JP6597808B2 - Polycarbonate diol and polyurethane using the same - Google Patents

Description

  The present invention relates to a polycarbonate diol useful as a raw material for a polycarbonate-based polyurethane and a polyurethane using the same.

  Conventionally, the raw material of the main soft segment part of polyurethane produced on an industrial scale is ether type typified by polytetramethylene glycol, polyester polyol type typified by adipate ester, polylactone type typified by polycaprolactone Or it is divided into the polycarbonate type represented by polycarbonate diol (nonpatent literature 1).

Among these, polyurethane using ether type is said to be inferior in heat resistance and weather resistance, although it is excellent in hydrolysis resistance, flexibility and stretchability. On the other hand, polyurethane using a polyester polyol type is improved in heat resistance and weather resistance, but has low ester group hydrolysis resistance and cannot be used depending on the application.
On the other hand, polyurethanes using polylactone type are considered to be superior in hydrolysis resistance compared to polyurethanes using polyester polyol type, but the hydrolysis is completely suppressed due to the presence of ester groups. I can't. In addition, it has been proposed to mix these polyester polyol type, ether type and polylactone type and use them as raw materials for polyurethane, but it has not been possible to completely compensate for the respective drawbacks.

On the other hand, polyurethane using polycarbonate type typified by polycarbonate diol is considered the best durability grade in heat resistance and hydrolysis resistance, including durable films, artificial leather for automobiles, (water-based) paints, Widely used as an adhesive.
However, the polycarbonate diol that is currently commercially available is a polycarbonate diol synthesized mainly from 1,6-hexanediol, but since this has high crystallinity, when it is made into polyurethane, the cohesiveness of the soft segment In particular, there is a problem that flexibility, elongation, bending, or elastic recovery at low temperatures is poor, and the application is limited. Furthermore, it has been pointed out that the artificial leather made from this polyurethane as a raw material has a hard texture and has a "feel" that is worse than natural leather.
In order to solve the above problems, polycarbonate diols having various structures have been proposed.

  For example, there is a method in which 1,6-hexanediol and another dihydroxy compound are used as raw materials to form a copolymerized polycarbonate diol, specifically, a polycarbonate copolymerized using 1,6-hexanediol and 1,4-butanediol as raw materials. Diol (Patent Document 1), Polycarbonate diol (Patent Document 2) copolymerized from 1,6-hexanediol and 1,5-pentanediol as raw materials, Copolymerized from 1,3-propanediol and other dihydroxy compounds as raw materials A polycarbonate diol (Patent Document 3) has been proposed.

  In addition, a method using a dihydroxy compound having a substituent in the main chain has been proposed as an effective method for inhibiting the crystallinity of the site derived from the dihydroxy compound. For example, 2-methyl-1,3-propanediol and other alkylenes have been proposed. There are polycarbonate diol copolymerized using glycol as a raw material (Patent Document 4), polycarbonate diol copolymerized using 3-methyl-1,5-pentanediol and another alkylene diol as raw materials (Patent Document 5), and the like.

In addition, polyurethanes using polycarbonate diols made from 2-methyl-1,8-octanediol or 1,9-nonanediol, which are long-chain diols, have been proposed. (Patent Document 6)
Furthermore, as a polycarbonate diol excellent in chemical resistance, low temperature characteristics, and heat resistance, a polycarbonate diol having an average diol carbon number exceeding 6 has been proposed. (Patent Document 7)
Also, by using a mixture of polycarbonate diol made from diols having 3 to 6 carbon atoms and polycarbonate diol made from diols having 7 to 12 carbon atoms, flexibility and chemical resistance are improved. A polyurethane using such a polycarbonate diol has been proposed. (Patent Documents 8 to 10)

JP-A-5-51428 JP-A-2-289616 International Publication No. 2002/070584 Pamphlet International Publication No. 2006/088152 Pamphlet JP 60-195117 A Japanese Examined Patent Publication No. 3-54967 JP 2000-95852 A Japanese Patent No. 04177318 Japanese Patent No. 05067544 JP 2008-106415 A

"Basics and Applications of Polyurethane", pages 96-106, supervised by Katsuharu Matsunaga, issued by CMC Publishing Co., Ltd., November 2006

  However, these conventionally known techniques, for example, the polycarbonate diols described in Patent Documents 1 to 3, etc., have insufficient low temperature characteristics when used as polyurethane. Further, the polycarbonate diols described in Patent Documents 4 to 5 have poor chemical resistance and heat resistance when used as polyurethane. Furthermore, the polycarbonate diol described in Patent Document 6 has poor chemical resistance and wear resistance when used as polyurethane. In addition, the short-chain diol substantially used in the polycarbonate diols of Patent Documents 7 to 10 and the like has 6 carbon atoms, and has poor chemical resistance when used as a polyurethane. An object of the present invention is to provide a polycarbonate diol, which is a raw material for polyurethane having an excellent balance of physical properties such as chemical resistance, low temperature characteristics, and heat resistance, which has not been achieved by the prior art.

  As a result of intensive studies to solve the above problems, the present inventors have obtained a structural unit derived from a compound represented by the following formula (A) and a structure derived from a compound represented by the following formula (B). A polycarbonate diol containing a unit, wherein the polycarbonate diol having a hydroxyl value of 20 mg-KOH / g or more and 450 mg-KOH / g or less is a raw material for polyurethane having a good balance of chemical resistance, low temperature characteristics and heat resistance It discovered that it was diol, and resulted in this invention.

That is, the gist of the present invention is as follows. That is, the gist of the present invention is as follows.
[1] A polycarbonate diol containing a structural unit derived from a compound represented by the following formula (A) and a structural unit derived from a compound represented by the following formula (B), and having a hydroxyl value of 20
mg-KOH / g or more 450mg-KOH / g Ri der below,
A structural unit derived from a compound represented by the following formula (A) and a compound represented by the following formula (B)
From the ratio of the structural units is a molar ratio 70: 30 to 99: polycarbonate diol according to claim 1 der Rukoto.
HO—R ¹ —OH (A)
HO—R ² —OH (B)

(In the above formula (A), R ¹ represents a substituted or unsubstituted divalent alkylene group having 3 to 5 carbon atoms. In the above formula (B), R ² represents a substituted or unsubstituted carbon number 9. ~ Represents a divalent alkylene group having 20 carbon atoms.
[2] The total ratio of the structural unit derived from the compound represented by the formula (A) and the structural unit derived from the compound represented by the formula (B) is 50 mol in all the structural units of the polycarbonate diol. % Of the polycarbonate diol as described in [1] above.
[3] The compound represented by the formula (B) is 1,9-nonanediol or 1,10-decane.
Diol, 1,11-undecanediol, 1,12-dodecanediol, 1,13-to
Lidecanediol, 1,14-tetradecanediol, 1,16-hexadecanediol
, 1,18-octadecanediol, and 1,20-eicosanediol
The polycarbonate diol according to the above [1] or [2], which is at least one selected compound .
[4] The polycarbonate diol according to any one of the above [1] to [3], wherein an average number of carbon atoms of a dihydroxy compound obtained by hydrolyzing the polycarbonate diol is 4 or more and 5.5 or less.
[5] The polycarbonate diol according to any one of [1] to [4], wherein the hydroxyl value is 20 mg-KOH / g or more and 60 mg-KOH / g or less.
[6] The above [1] to [5], wherein the compound represented by the formula (A) is at least one compound selected from the group consisting of 1,3-propanediol and 1,4-butanediol. Any one of the polycarbonate diols.
[7] The compound represented by the formula (B) is 1,9, is at least one compound selected from the group consisting of 1,10-decanediol, and 1,12-dodecanediol The polycarbonate diol according to any one of the above [1] to [6].
[8] The polycarbonate diol according to any one of [1] to [7], wherein at least one of the compound represented by the formula (A) and the compound represented by the formula (B) is derived from a plant. .
[9] Is it an ester compound of a cyclic lactone, a dicarboxylic acid compound and a dicarboxylic acid compound?
An ester group is introduced by reaction with at least one compound selected from the group consisting of
The polycarbonate diol according to any one of [1] to [8].
[ 10 ] A polyurethane comprising the polycarbonate diol according to any one of [1] to [ 9 ].
[ 11 ] Artificial leather or synthetic leather produced using the polyurethane described in [ 10 ] above.
[ 12 ] A paint or coating agent produced using the polyurethane described in [ 10 ] above.
[ 13 ] An elastic fiber produced using the polyurethane described in [ 10 ].
[ 14 ] A water-based polyurethane paint produced using the polyurethane described in [ 10 ] above.
[ 15 ] A pressure-sensitive adhesive or adhesive produced using the polyurethane described in [ 10 ] above.
[ 16 ] An active energy ray-curable polymer composition using the polycarbonate diol according to any one of [1] to [ 9 ].
[ 17 ] A method for producing the polycarbonate diol according to any one of [1] to [7] above, wherein the compound represented by the following formula (A) and the compound represented by the following formula (B): A method for producing a polycarbonate diol, wherein a polycondensation is carried out by transesterification using a carbonate compound.
HO—R ¹ —OH (A)
HO—R ² —OH (B)

(In the formula (A), R ¹ represents a substituted or unsubstituted divalent alkylene group having 3 to 5 carbon atoms, and in the formula (B), R ² represents an unsubstituted 9 to carbon atoms. This represents a divalent alkylene group of formula 20.

  The polyurethane produced using the polycarbonate diol of the present invention has an excellent balance of chemical resistance, low temperature characteristics, and heat resistance, and is suitable for use in elastic fibers, synthetic or artificial leather, paints, and high performance elastomers. It is extremely useful in industry.

Hereinafter, although the form of this invention is demonstrated in detail, this invention is not limited to the following embodiment, Various deformation | transformation can be implemented within the range of the summary.
Here, in the present specification, “mass%” and “weight%”, “mass ppm” and “weight ppm”, and “mass part” and “weight part” are synonymous, respectively. In addition, when “ppm” is simply described, it indicates “weight ppm”.

[1. Polycarbonate diol]
The polycarbonate diol of the present invention is a polycarbonate diol including a structural unit derived from a compound represented by the following formula (A) and a structural unit derived from a compound represented by the following formula (B), and has a hydroxyl value of 20 mg. -KOH / g or more and 450 mg-KOH / g or less.
HO—R ¹ —OH (A)
HO—R ² —OH (B)

(In the above formula (A), R ¹ represents a substituted or unsubstituted divalent alkylene group or polymethylene group having 3 to 5 carbon atoms, and in the above formula (B), R ² represents 8 to carbon atoms. (It represents a substituted or unsubstituted divalent alkylene group or polymethylene group represented by Formula 20.)

<1-1. Structural features>
The structural unit derived from the compound represented by the formula (A) according to the present invention is represented by the following formula (C), for example. Moreover, the structural unit derived from the compound represented by the said formula (B) is represented by the following formula (D), for example.

(In the above formula (C), R ¹ represents a substituted or unsubstituted divalent alkylene group having 3 to 5 carbon atoms or a polymethylene group.)

(In the above formula (D), R ² represents a substituted or unsubstituted divalent alkylene or polymethylene group having 8 to 20 carbon atoms.)
In the formula (C), R ¹ may be one kind or plural kinds. In the formula (D), R ² may be one kind or plural kinds.
In the above formula (C), R ¹ is a substituted or unsubstituted divalent alkylene group having 3 to 5 carbon atoms, and the chemical resistance, low temperature characteristics, and heat resistance are improved. the number of the substituents is preferably 1 or less in ^1, unsubstituted more preferably. When there is a substituent, the smaller the number of carbon atoms of the substituent, the better the chemical resistance, the low temperature characteristics, and the heat resistance, and therefore the number of carbons is preferably 2 or less, and more preferably 1 or less.

In the formula (D), R ² is a substituted or unsubstituted divalent alkylene group having 8 to 20 carbon atoms or a polymethylene group, and has good chemical resistance, low temperature characteristics, and heat resistance. Accordingly, the number of substituents in R ² is preferably 1 or less, and more preferably unsubstituted. When there is a substituent, the smaller the number of carbon atoms of the substituent, the smaller the number of carbon atoms of the substituent, the better the chemical resistance, low temperature characteristics, and heat resistance. Further preferred.

Furthermore, in the above formula (C) and the formula (D), the following is calculated by the equation, the ratio is 10% or less to the total number of carbon atoms of R ¹ and R ² of the number of carbon atoms of the substituent in R ¹ and R ² Is preferably 5% or less, more preferably 3% or less, particularly preferably 2% or less, and most preferably 0%.

  The polycarbonate diol of the present invention includes a structural unit derived from the compound represented by the formula (A) and a structural unit derived from the compound represented by the formula (B). By including the structural unit derived from the compound represented by the formula (A) and the structural unit derived from the compound represented by the formula (B), good chemical resistance and low temperature characteristics when made into a polyurethane are obtained. Obtainable. Furthermore, the ratio between the structural unit derived from the compound represented by the formula (A) and the structural unit derived from the compound represented by the formula (B) (hereinafter sometimes referred to as “(A) :( B)”). Is a molar ratio of (A) :( B) = 50: 50 to 99: 1, preferably 60:40 to 97: 3, more preferably 70:30 to 95: 5, and 80 : 20 to 90:10 is most preferable. If the content ratio of the structural unit derived from the compound represented by the formula (A) is too large, the low temperature characteristics when polyurethane is used may not be sufficient. When the content ratio of the structural unit derived from the compound represented by the formula (A) is too small, chemical resistance when polyurethane is used may not be sufficient.

  Furthermore, when the average number of carbon atoms of the dihydroxy compound obtained by hydrolyzing the polycarbonate diol is 4 or more and 5.5 or less, good chemical resistance, heat resistance, and abrasion resistance can be obtained when the polyurethane is made. it can. The upper limit of the average carbon number is preferably 5.3, more preferably 5.2, and even more preferably 5.1. The lower limit of the average carbon number is preferably 4.3, more preferably 4.5, and even more preferably 4.7. If it is less than the lower limit, the low-temperature characteristics may be insufficient, and if it exceeds the upper limit, chemical resistance, heat resistance, and wear resistance may be insufficient.

  The average carbon number of the dihydroxy compound obtained by hydrolyzing the polycarbonate diol in the present invention is determined from the result of gas chromatography analysis of the dihydroxy compound obtained by hydrolyzing the polycarbonate diol by heating in the presence of an alkali. be able to. Specifically, it is calculated from the carbon number of the dihydroxy compound obtained by hydrolyzing the polycarbonate diol and the molar ratio of the dihydroxy compound to the total dihydroxy compound.

  The total ratio of the structural unit derived from the compound represented by the formula (A) and the structural unit derived from the compound represented by the formula (B) to the total structural unit of the polycarbonate diol is chemical resistance, low temperature From the balance of physical properties, it is preferably 50 mol% or more, more preferably 70 mol% or more, further preferably 80 mol% or more, particularly preferably 90 mol% or more, and most preferably 95 mol% or more.

If the polycarbonate diol of the present invention contains a structural unit derived from the compound represented by the formula (A) and a structural unit derived from the compound represented by the formula (B), these are copolymers. Alternatively, it may be a mixture of different kinds of polycarbonate diols, but is preferably a copolymer because of low temperature characteristics and good flexibility. In the case of a copolymer, a block copolymer or a random copolymer may be used, but the polycarbonate diol of the random copolymer is more preferable because of low temperature characteristics and flexibility.
The ratio of the structural unit derived from each dihydroxy compound to the total structural unit of the polycarbonate diol of the present invention can be determined by analyzing each dihydroxy compound obtained by hydrolyzing the polycarbonate diol with an alkali by gas chromatography.

<1-2. Dihydroxy Compound>
The compound represented by the formula (A), which is a dihydroxy compound used as a raw material for the polycarbonate diol of the present invention, is 1,3-propanediol, 2-methyl-1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 2-methyl-1,4-butanediol, 1,5-pentanediol and the like can be mentioned. Among these, 1,3-propanediol, 1,4-butanediol, and 1,5-propanediol are preferred because of excellent balance between chemical resistance and low-temperature characteristics when polyurethane is used, and 1,3-propanediol, 4-butanediol is more preferred, and 1,4-butanediol is even more preferred. In addition, the compound represented by the said formula (A) may be 1 type, or may be multiple types.

  The compound represented by the formula (B) is 1,8-octanediol, 2-methyl-1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol, 1,12-dodecanediol, 1,13-tridecanediol, 1,14-tetradecanediol, 1,16-hexadecanediol, 1,18-octadecanediol, 1,12-octadecanediol, 1,20-eicosanediol Etc. Among these, 1,8-octanediol, 2-methyl-1,8-octanediol, 1,9-nonanediol, and 1,10-decanediol have excellent balance of chemical resistance and low temperature characteristics when polyurethane is used. 1,11-undecanediol and 1,12-dodecanediol are preferable, and 2-methyl-1,8-octanediol, 1,9-nonanediol, 1,10-decanediol and 1,12-dodecanediol are more preferable. 1,9-nonanediol, 1,10-decanediol, and 1,12-dodecanediol are more preferable, 1,10-decanediol and 1,12-dodecanediol are particularly preferable, and 1,10-decanediol is preferable. Most preferred. In addition, the compound represented by the said formula (B) may be 1 type, or may be multiple types.

In the production of the polycarbonate diol of the present invention, unless the effect of the present invention is impaired, the compound represented by the above formula (A) and the dihydroxy compound other than the compound represented by the above formula (B) (with other dihydroxy compounds and May be used). Specific examples include linear dihydroxy compounds, dihydroxy compounds having an ether group, dihydroxy compounds having a branched chain, and dihydroxy compounds having a cyclic group. However, when other dihydroxy compounds are used, in order to effectively obtain the effects of the present invention, the proportion of structural units derived from other dihydroxy compounds is preferably 50 mol% or less with respect to the total structural units of the polycarbonate diol. 30 mol% or less is more preferable, 20 mol% or less is more preferable, and 10 mol% or less is the most preferable. When the proportion of structural units derived from other dihydroxy compounds is large, the balance between chemical resistance and low temperature characteristics may be impaired.

The compound represented by the formula (A) is preferably derived from a plant from the viewpoint of reducing environmental load. Examples of the compound represented by the formula (A) applicable as a plant origin include 1,3-propanediol, 1,4-butanediol, 1,5-propanediol and the like.
The compound represented by the formula (B) is preferably derived from a plant from the viewpoint of reducing environmental load. Examples of the compound represented by the formula (B) applicable as a plant-derived material include 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol, 1,12-dodecanediol, and 1,13. -Tridecanediol, 1,12-octadecanediol, 1,20-eicosanediol and the like.

  As a plant-derived dihydroxy compound, for example, in the case of 1,4-butanediol, succinic acid, succinic anhydride, succinic acid ester, maleic acid, maleic acid anhydride, maleic acid ester, tetrahydrofuran and γ obtained by the fermentation method -1,4-butanediol may be produced by chemical synthesis from butyrolactone or the like, 1,4-butanediol may be produced directly by fermentation, or 1,3-butadiene obtained by fermentation 1,4-butanediol may be produced from Among them, a method of directly producing 1,4-butanediol by a fermentation method and a method of obtaining 1,4-butanediol by hydrogenating succinic acid with a reduction catalyst are efficient and preferable.

In the case of 1,3-propanediol, 3-hydroxypropionaldehyde is produced from glycerol, glucose, and other sugars by fermentation, and then converted to 1,3-propanediol, and then fermented from glucose and other sugars. It can be obtained by directly producing 1,3-propanediol by the method.
1,10-decanediol can be synthesized by synthesizing sebacic acid from castor oil by alkali melting and hydrogenating directly or after the esterification reaction.

<1-3. Carbonate compound>
The carbonate compound (sometimes referred to as “carbonic acid diester”) that can be used in the production of the polycarbonate diol of the present invention is not limited as long as the effects of the present invention are not impaired, but examples thereof include dialkyl carbonate, diaryl carbonate, and alkylene carbonate. It is done. Of these, diaryl carbonate is preferred from the viewpoint of reactivity.
Specific examples of the carbonate compound include dimethyl carbonate, diethyl carbonate, dibutyl carbonate, diphenyl carbonate, ethylene carbonate and the like, and diphenyl carbonate is preferable.

<1-4. Transesterification Catalyst>
The polycarbonate diol of the present invention can be produced by polycondensing a compound represented by the above formula (A), a compound represented by the above formula (B) and a carbonate compound by a transesterification reaction.
In the production of the polycarbonate diol of the present invention, a transesterification catalyst (hereinafter sometimes referred to as a catalyst) can be used as necessary to promote polymerization. In that case, when an excessively large amount of catalyst remains in the obtained polycarbonate diol, the reaction may be inhibited or the reaction may be excessively promoted when a polyurethane is produced using the polycarbonate diol.

For this reason, the amount of catalyst remaining in the polycarbonate diol is not particularly limited, but is preferably 100 ppm or less, more preferably 50 ppm or less, and even more preferably 10 ppm or less as the content in terms of catalyst metal.
As the transesterification catalyst, any compound that is generally considered to have transesterification ability can be used without limitation.

  Examples of transesterification catalysts include lithium, sodium, potassium, rubidium, cesium and other periodic table group 1 metal compounds; magnesium, calcium, strontium, barium and other periodic table group 2 metal compounds; titanium, zirconium Periodic Table Group 4 metal compounds such as Hafnium; Periodic Table Group 5 metal compounds such as hafnium; Periodic Table Group 9 metal compounds such as cobalt; Periodic Table Group 12 metal compounds such as zinc; Periodic table group 13 metal compounds; germanium, tin, lead, etc. periodic table group 14 metal compounds; antimony, bismuth, etc. periodic table group 15 metal compounds; lanthanide metals such as lanthanum, cerium, europium, ytterbium And the like. Among these, from the viewpoint of increasing the transesterification reaction rate, compounds of Group 1 metal of the periodic table, compounds of Group 2 metal of the periodic table, compounds of Group 4 metal of the periodic table, compounds of Group 5 metal of the periodic table, Periodic table Group 9 metal compound, Periodic table Group 12 metal compound, Periodic table Group 13 metal compound, Periodic table Group 14 metal compound are preferred, Periodic table Group 1 metal compound, Periodic table A compound of Group 2 metal is more preferable, and a compound of Group 2 metal of the periodic table is more preferable. Among the compounds of Group 1 metals of the periodic table, lithium, potassium, and sodium compounds are preferable, lithium and sodium compounds are more preferable, and sodium compounds are more preferable. Among the compounds of Group 2 metals of the periodic table, magnesium, calcium and barium compounds are preferred, calcium and magnesium compounds are more preferred, and magnesium compounds are more preferred. These metal compounds are mainly used as hydroxides and salts. Examples of salts when used as a salt include halide salts such as chloride, bromide and iodide; carboxylates such as acetate, formate and benzoate; methanesulfonic acid, toluenesulfonic acid and trifluoro Examples thereof include sulfonates such as romethanesulfonic acid; phosphorus-containing salts such as phosphates, hydrogen phosphates, and dihydrogen phosphates; acetylacetonate salts. The catalyst metal can also be used as an alkoxide such as methoxide or ethoxide.

  Among these, preferably, acetate, nitrate, sulfate, carbonate, phosphate, hydroxide, halide, alkoxide of at least one metal selected from Group 2 metals of the periodic table is used, More preferred are group 2 metal acetates, carbonates, and hydroxides of the periodic table, more preferred are magnesium, calcium acetates, carbonates, and hydroxides, and particularly preferred are magnesium and calcium. Acetate is used, most preferably magnesium acetate.

<1-5. Molecular chain end>
The molecular chain terminal of the polycarbonate diol of the present invention is mainly a hydroxyl group. However, in the case of a polycarbonate diol obtained by the reaction of a dihydroxy compound and a carbonate compound, there is a possibility that some molecular chain terminals are not hydroxyl groups as impurities. As specific examples thereof, the molecular chain terminal is an alkyloxy group or an aryloxy group, and many have a structure derived from a carbonate compound.

For example, when diphenyl carbonate is used as the carbonate compound, a phenoxy group (PhO-) as an aryloxy group, a methoxy group (MeO-) as an alkyloxy group when dimethyl carbonate is used, and an ethoxy group when diethyl carbonate is used. (EtO-), when ethylene carbonate is used, a hydroxyethoxy group (HOCH2CH2O-) may remain as a molecular chain end (where Ph represents a phenyl group, Me represents a methyl group, and Et represents ethyl Represents a group).

  The molecular chain terminal of the polycarbonate diol of the present invention has the number of terminals derived from the compound represented by the formula (A) and the number of terminals derived from the compound represented by the formula (B) with respect to the total number of terminals. The total number ratio is preferably 80 mol% or more, more preferably 90 mol% or more, further preferably 95 mol% or more, particularly preferably 97 mol% or more, and most preferably 99 mol% or more. By setting it within the above range, it becomes easy to obtain a desired molecular weight when polyurethane is used, and it becomes possible to provide a polyurethane raw material having an excellent balance of chemical resistance and low temperature characteristics.

The ratio of the number of terminal groups in which the molecular chain terminal of the polycarbonate diol is derived from the carbonate compound is preferably 10 mol% or less, more preferably 5 mol% or less, and still more preferably 3 mol%, based on the total number of terminals. Hereinafter, it is particularly preferably 1 mol% or less.
The lower limit of the hydroxyl value of the polycarbonate diol of the present invention is 20 mg-KOH / g, preferably 25 mg-KOH / g, more preferably 30 mg-KOH / g, still more preferably 35 mg-KOH / g. The upper limit is 450 mg-KOH / g, preferably 230 mg-KOH / g, more preferably 150 mg-KOH / g, more preferably 120 mg-KOH / g, still more preferably 75 mg-KOH / g, particularly preferably 60 mg. -KOH / g, most preferably 45 mg-KOH / g. If the hydroxyl value is less than the above lower limit, the viscosity may be too high and handling during polyurethane formation may be difficult. If the upper limit is exceeded, physical properties such as flexibility and low-temperature characteristics may be insufficient when polyurethane is used.

<1-6. Molecular Weight / Molecular Weight Distribution>
The lower limit of the number average molecular weight (Mn) determined from the hydroxyl value of the polycarbonate diol of the present invention is preferably 250, more preferably 300, still more preferably 400. On the other hand, the upper limit is preferably 5,000, more preferably 4,000, and still more preferably 3,000. If the Mn of the polycarbonate diol is less than the lower limit, sufficient flexibility may not be obtained when urethane is used. On the other hand, if the upper limit is exceeded, the viscosity increases, and handling during polyurethane formation may be impaired.

The weight average molecular weight / number average molecular weight (Mw / Mn), which is the molecular weight distribution of the polycarbonate diol of the present invention, is not particularly limited, but the lower limit is preferably 1.5, and more preferably 1.8. The upper limit is preferably 3.5, more preferably 3.0. When the molecular weight distribution exceeds the above range, the properties of the polyurethane produced using this polycarbonate diol tend to become hard at low temperatures and decrease in elongation, and an attempt is made to produce a polycarbonate diol having a molecular weight distribution less than the above range. Then, an advanced purification operation such as removing the oligomer may be necessary.
The weight average molecular weight is a polystyrene-equivalent weight average molecular weight, and the number-average molecular weight is a polystyrene-equivalent number average molecular weight, and can be usually determined by measurement of gel permeation chromatography (sometimes abbreviated as GPC).

<1-7. Ratio of raw materials used>
In the production of the polycarbonate diol of the present invention, the amount of the carbonate compound used is not particularly limited, but is usually a molar ratio with respect to a total of 1 mol of the dihydroxy compound, and the lower limit is preferably 0.35, more preferably 0.50, still more preferably. Is 0.60, and the upper limit is preferably 1.00, more preferably 0.98, and still more preferably 0.97. If the amount of the carbonate compound used exceeds the above upper limit, the proportion of the polycarbonate diol end group that is not a hydroxyl group may increase or the molecular weight may not fall within the predetermined range. If the amount is less than the lower limit, the polymerization does not proceed to the predetermined molecular weight. There is a case.

<1-8. Catalyst Deactivator>
As described above, when a catalyst is used in the polymerization reaction, the catalyst is usually left in the obtained polycarbonate diol, and due to the remaining catalyst, heating of the polycarbonate diol causes an increase in molecular weight, composition change, deterioration of color tone, etc. Or control of the polyurethane-forming reaction may not be possible. In order to suppress the influence of the remaining catalyst, it is preferable to inactivate the transesterification catalyst by adding substantially equimolar amount of, for example, a phosphorus compound to the transesterification catalyst used. Further, after the addition, the transesterification catalyst can be efficiently inactivated by heat treatment or the like as described later. As the phosphorus compound, phosphoric acid and phosphorous acid are preferable, and phosphoric acid is more preferable because the effect is large in a small amount.

  Examples of phosphorus compounds used for inactivating the transesterification catalyst include inorganic phosphoric acid such as phosphoric acid and phosphorous acid, dibutyl phosphate, tributyl phosphate, trioctyl phosphate, triphenyl phosphate, And organic phosphate esters such as triphenyl phosphate.

These may be used alone or in combination of two or more.
Although the amount of the phosphorus compound used is not particularly limited, as described above, it may be approximately equimolar with the transesterification catalyst used, and specifically, with respect to 1 mol of the transesterification catalyst used. The upper limit is preferably 5 mol, more preferably 2 mol, and the lower limit is preferably 0.6 mol, more preferably 0.8 mol, and still more preferably 1.0 mol. When a smaller amount of phosphorus-based compound is used, heating the polycarbonate diol may result in an increase in the molecular weight of the polycarbonate diol, composition change, color tone deterioration, etc., or inactivation of the transesterification catalyst is not sufficient. When the polycarbonate diol is used as a raw material for polyurethane production, for example, the reactivity of the polycarbonate diol with respect to the isocyanate group may not be sufficiently lowered. In addition, when a phosphorus compound exceeding this range is used, the obtained polycarbonate diol is colored or when the polycarbonate diol is used as a raw material, the polyurethane is easily hydrolyzed, and the phosphorus compound bleeds out. There is a possibility.

The inactivation of the transesterification catalyst by adding a phosphorus compound can be performed at room temperature, but it is more efficient when heat-treated. The temperature of this heat treatment is not particularly limited, but the upper limit is preferably 180 ° C., more preferably 150 ° C., still more preferably 120 ° C., even more preferably 100 ° C., and the lower limit is preferably 50 ° C. Preferably it is 60 degreeC, More preferably, it is 70 degreeC. If the temperature is lower than this, it takes time to inactivate the transesterification catalyst, which is not efficient, and the degree of inactivation may be insufficient. On the other hand, at a temperature exceeding 180 ° C., the obtained polycarbonate diol may be colored.
The time for reacting with the phosphorus compound is not particularly limited, but is usually 0.1 to 5 hours.

<1-9. Residual monomers, etc.>
When an aromatic carbonic acid diester such as diphenyl carbonate is used as a raw material, phenols are by-produced during the production of the polycarbonate diol. Since phenols are monofunctional compounds, they may be an inhibitory factor in the production of polyurethane, and the urethane bonds formed by phenols are weak in their bonding strength, so they can be heated by subsequent processes. It may dissociate, causing isocyanates and phenols to be regenerated and causing problems. Moreover, since phenols are also stimulating substances, it is preferable that the residual amount of phenols in the polycarbonate diol is smaller. Specifically, the weight ratio to the polycarbonate diol is preferably 1000 ppm or less, more preferably 500 ppm or less, still more preferably 300 ppm or less, and particularly preferably 100 ppm or less.
In order to reduce the phenols in the polycarbonate diol, as described later, the pressure of the polymerization reaction of the polycarbonate diol may be set to a high vacuum of 1 kPa or less as an absolute pressure, or thin film distillation or the like may be performed after the polymerization of the polycarbonate diol. It is valid.

  In polycarbonate diol, the carbonic acid diester used as a raw material at the time of manufacture may remain. The residual amount of the carbonic acid diester in the polycarbonate diol is not limited, but a smaller amount is preferable, and the upper limit of the weight ratio with respect to the polycarbonate diol is preferably 5% by weight, more preferably 3% by weight, still more preferably 1% by weight. is there. If the carbonic diester content of the polycarbonate diol is too large, the reaction during polyurethane formation may be inhibited. On the other hand, the lower limit is not particularly limited, but is preferably 0.1% by weight, more preferably 0.01% by weight, and still more preferably 0% by weight.

  In polycarbonate diol, the dihydroxy compound used at the time of manufacture may remain. The residual amount of the dihydroxy compound in the polycarbonate diol is not limited, but a smaller amount is preferable, and the weight ratio with respect to the polycarbonate diol is preferably 1% by weight or less, more preferably 0.1% by weight or less, and still more preferably. Is 0.05% by weight or less. If the residual amount of the dihydroxy compound in the polycarbonate diol is large, the molecular length of the soft segment portion when polyurethane is used may be insufficient, and desired physical properties may not be obtained.

  In polycarbonate diol, the cyclic carbonate (cyclic oligomer) byproduced in the case of manufacture may be contained. For example, when 1,3-propanediol is used as the compound represented by the formula (A), 1,3-dioxan-2-one or a compound in which two or more of these are converted to a cyclic carbonate is used. It may be produced and contained in polycarbonate diol. These compounds may cause side reactions in the polyurethane formation reaction and cause turbidity. Therefore, the pressure of the polymerization reaction of the polycarbonate diol is set to a high vacuum of 1 kPa or less as an absolute pressure, or the synthesis of the polycarbonate diol is performed. It is preferable to remove as much as possible by performing thin film distillation or the like later. The content of these cyclic carbonates contained in the polycarbonate diol is not limited, but is preferably 3% by weight or less, more preferably 1% by weight or less, and still more preferably 0.5% by weight or less as a weight ratio to the polycarbonate diol. .

[2. Polyurethane]
Polyurethane can be produced using the above-described polycarbonate diol of the present invention.
The process for producing the polyurethane of the present invention using the polycarbonate diol of the present invention usually employs known polyurethane reaction conditions for producing a polyurethane.

For example, the polyurethane of the present invention can be produced by reacting the polycarbonate diol of the present invention with a polyisocyanate and a chain extender in the range of room temperature to 200 ° C.
In addition, the polycarbonate diol of the present invention and an excess of polyisocyanate are first reacted to produce a prepolymer having an isocyanate group at the terminal, and the degree of polymerization is increased using a chain extender to produce the polyurethane of the present invention. I can do it.

<2-1. Polyisocyanate>
Examples of the polyisocyanate used for producing a polyurethane using the polycarbonate diol of the present invention include various known polyisocyanate compounds such as aliphatic, alicyclic or aromatic.
For example, tetramethylene diisocyanate, hexamethylene diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, 2,4,4-trimethylhexamethylene diisocyanate, lysine diisocyanate and dimerized isocyanate in which the carboxyl group of dimer acid is converted to an isocyanate group Aliphatic diisocyanates; 1,4-cyclohexane diisocyanate, isophorone diisocyanate, 1-methyl-2,4-cyclohexane diisocyanate, 1-methyl-2,6-cyclohexane diisocyanate, 4,4′-dicyclohexylmethane diisocyanate and 1,3-bis (Isocyanatomethyl) cycloaliphatic diisocyanates such as cyclohexane; xylylene diisocyanate, 4,4′-diphenyldi Cyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, m-phenylene diisocyanate, p-phenylene diisocyanate, 4,4'-diphenylmethane diisocyanate, 4,4'-diphenyldimethylmethane diisocyanate, 4,4 ' Dibenzyl diisocyanate, dialkyl diphenylmethane diisocyanate, tetraalkyl diphenylmethane diisocyanate, 1,5-naphthylene diisocyanate, 3,3′-dimethyl-4,4′-biphenylene diisocyanate, polymethylene polyphenyl isocyanate, phenylene diisocyanate and m-tetramethyl And aromatic diisocyanates such as xylylene diisocyanate. These may be used alone or in combination of two or more.

  Among these, 4,4′-diphenylmethane diisocyanate (hereinafter sometimes referred to as “MDI”), hexamethylene diisocyanate, a point where the balance of physical properties of the obtained polyurethane is preferable, and a large amount can be obtained industrially at low cost. 4,4′-dicyclohexylmethane diisocyanate and isophorone diisocyanate are preferred.

<2-2. Chain extender>
The chain extender used in producing the polyurethane of the present invention is a low molecular weight compound having at least two active hydrogens that react with isocyanate groups when producing a prepolymer having an isocyanate group, which will be described later. Usually, a polyol, a polyamine, etc. can be mentioned.

Specific examples thereof include ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, and 1,9-nonanediol. Linear diols such as 1,10-decanediol and 1,12-dodecanediol; 2-methyl-1,3-propanediol, 2,2-dimethyl-1,3-propanediol, 2,2-diethyl -1,3-propanediol, 2-methyl-2-propyl-1,3-propanediol, 2,4-heptanediol, 1,4-dimethylolhexane, 2-ethyl-1,3-hexanediol, 2 2,4-trimethyl-1,3-pentanediol, 2-methyl-1,8-octanediol, 2-butyl-2-ethyl-1,3-propanedi Diols having a branched chain such as diol and dimer diol; diols having an ether group such as diethylene glycol and propylene glycol; 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, 1,4-dihydroxyethylcyclohexane, etc. Diols having an alicyclic structure, diols having an aromatic group such as xylylene glycol, 1,4-dihydroxyethylbenzene, 4,4′-methylenebis (hydroxyethylbenzene); glycerin, trimethylolpropane, pentaerythritol, etc. Polyols; hydroxyamines such as N-methylethanolamine and N-ethylethanolamine; ethylenediamine, 1,3-diaminopropane, hexamethylenediamine, triethylenetetramine, diethylenetri Min, isophorone diamine, 4,4′-diaminodicyclohexyl methane, 2-hydroxyethyl propylene diamine, di-2-hydroxyethyl ethylene diamine, di-2-hydroxyethyl propylene diamine, 2-hydroxypropyl ethylene diamine, di-2-hydroxypropyl Polyamines such as ethylenediamine, 4,4′-diphenylmethanediamine, methylenebis (o-chloroaniline), xylylenediamine, diphenyldiamine, tolylenediamine, hydrazine, piperazine, N, N′-diaminopiperazine; and water be able to.

These chain extenders may be used alone or in combination of two or more.
Among them, 1,4-butanediol (hereinafter sometimes referred to as 1,4BD), 1,5 is preferable in that the balance of physical properties of the obtained polyurethane is preferable, and a large amount can be obtained industrially at low cost. -Pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,4-cyclohexanedimethanol, 1,4-dihydroxyethylcyclohexane, ethylenediamine, 1,3-diaminopropane, isophoronediamine, and 4,4′-diaminodicyclohexylmethane are preferred.
The chain extender in the case of producing a prepolymer having a hydroxyl group, which will be described later, is a low molecular weight compound having at least two isocyanate groups, specifically <2-1. And polyisocyanates>.

<2-3. Chain terminator>
In producing the polyurethane of the present invention, a chain terminator having one active hydrogen group can be used as necessary for the purpose of controlling the molecular weight of the resulting polyurethane.
These chain terminators include aliphatic monools such as methanol, ethanol, propanol, butanol and hexanol having one hydroxyl group, diethylamine, dibutylamine, n-butylamine, monoethanolamine and diethanolamine having one amino group. And aliphatic monoamines such as morpholine.
These may be used alone or in combination of two or more.

<2-4. Catalyst>
In the polyurethane formation reaction in producing the polyurethane of the present invention, an amine catalyst such as triethylamine, N-ethylmorpholine, triethylenediamine, or tin such as trimethyltin laurate, dibutyltin dilaurate, dioctyltin dilaurate, dioctyltin dineodecanate, etc. Known urethane polymerization catalysts typified by organic compounds such as organic metal salts such as titanium compounds and the like can also be used. A urethane polymerization catalyst may be used individually by 1 type, and may use 2 or more types together.

<2-5. Polyols Other than Polycarbonate Diol of the Present Invention>
In the polyurethane formation reaction in producing the polyurethane of the present invention, the polycarbonate diol of the present invention may be used in combination with other polyols as necessary. Here, the polyol other than the polycarbonate diol of the present invention is not particularly limited as long as it is used in normal polyurethane production, and examples thereof include polyether polyol, polyester polyol, polycaprolactone polyol, and polycarbonate polyol other than the present invention. can give. For example, when used in combination with a polyether-based polyol, a polyurethane having further improved low temperature characteristics, which is a feature of the polycarbonate diol of the present invention, can be obtained. Here, it is based on the combined weight of the polycarbonate diol of the present invention and other polyols. The weight ratio of the polycarbonate diol of the present invention is preferably 70% or more, more preferably 90% or more. If the weight ratio of the polycarbonate diol of the present invention is small, the balance of chemical resistance, low temperature characteristics and heat resistance, which are the characteristics of the present invention, may be lost.

In the present invention, the above-mentioned polycarbonate diol of the present invention can be modified for use in the production of polyurethane. As a modification method of the polycarbonate diol, a method of introducing an ether group by adding an epoxy compound such as ethylene oxide, propylene oxide or butylene oxide to the polycarbonate diol, a cyclic lactone such as ε-caprolactone, adipic acid, or succinic acid is used as the polycarbonate diol. There is a method of introducing an ester group by reacting with dicarboxylic acid compounds such as sebacic acid and terephthalic acid and ester compounds thereof. In the ether modification, the viscosity of the polycarbonate diol is lowered by modification with ethylene oxide, propylene oxide or the like, which is preferable for reasons such as handling. In particular, the polycarbonate diol of the present invention is modified with ethylene oxide or propylene oxide, so that the crystallinity of the polycarbonate diol is lowered and the flexibility at low temperature is improved. Since the water absorption and moisture permeability of the manufactured polyurethane are increased, the performance as artificial leather / synthetic leather may be improved. However, when the addition amount of ethylene oxide or propylene oxide increases, the physical properties such as mechanical strength, heat resistance, chemical resistance, etc. of the polyurethane produced using the modified polycarbonate diol are lowered. -50 wt% is suitable, preferably 5-40 wt%, more preferably 5-30 wt%. In addition, the method of introducing an ester group is preferable for reasons such as handling because the viscosity of the polycarbonate diol is reduced by modification with ε-caprolactone. The amount of ε-caprolactone added to the polycarbonate diol is preferably 5 to 50% by weight, preferably 5 to 40% by weight, and more preferably 5 to 30% by weight. When the added amount of ε-caprolactone exceeds 50% by weight, the hydrolysis resistance, chemical resistance, etc. of the polyurethane produced using the modified polycarbonate diol are lowered.

<2-6. Solvent>
A solvent may be used for the polyurethane formation reaction in producing the polyurethane of the present invention.
Preferred solvents include amide solvents such as dimethylformamide, diethylformamide, dimethylacetamide and N-methylpyrrolidone; sulfoxide solvents such as dimethyl sulfoxide; ketone solvents such as methyl ethyl ketone, cyclohexanone and methyl isobutyl ketone; tetrahydrofuran, dioxane and the like. Examples include ether solvents; ester solvents such as methyl acetate, ethyl acetate, and butyl acetate; and aromatic hydrocarbon solvents such as toluene and xylene. These solvents may be used alone or as a mixed solvent of two or more.

Among these, preferred organic solvents are methyl ethyl ketone, ethyl acetate, toluene, dimethylformamide, dimethylacetamide, N-methylpyrrolidone, dimethyl sulfoxide and the like.
Moreover, the polyurethane of an aqueous dispersion can also be manufactured from the polyurethane composition with which the polycarbonate diol of this invention, polydiisocyanate, and the said chain extender were mix | blended.

<2-7. Polyurethane production method>
As a method for producing the polyurethane of the present invention using the above-mentioned reaction reagent, a production method generally used experimentally or industrially can be used.
Examples thereof include a method in which the polycarbonate diol of the present invention, other polyols, polyisocyanate and chain extender are mixed and reacted (hereinafter sometimes referred to as “one-step method”), or first of the present invention. A method of reacting a polycarbonate diol, other polyol and polyisocyanate to prepare a prepolymer having isocyanate groups at both ends, and then reacting the prepolymer with a chain extender (hereinafter sometimes referred to as “two-stage method”). There is).

In the two-stage method, the polycarbonate diol of the present invention and other polyol are reacted with one or more equivalents of a polyisocyanate in advance to prepare a part of the terminal isocyanate intermediate corresponding to the soft segment of the polyurethane. Is. In this way, once the prepolymer is prepared and reacted with the chain extender, it may be easy to adjust the molecular weight of the soft segment part, and when it is necessary to ensure phase separation of the soft segment and the hard segment. Is useful.

<2-8. One-step method>
The one-stage method is also referred to as a one-shot method, and is a method in which the reaction is carried out by charging the polycarbonate diol of the present invention, other polyols, polyisocyanate and chain extender all at once.
The amount of polyisocyanate used in the one-stage method is not particularly limited, but the total number of hydroxyl groups of the polycarbonate diol of the present invention and other polyols and the total number of hydroxyl groups and amino groups of the chain extender is 1 equivalent. The lower limit is preferably 0.7 equivalents, more preferably 0.8 equivalents, still more preferably 0.9 equivalents, particularly preferably 0.95 equivalents, and the upper limit is preferably 3.0 equivalents, more preferably Is 2.0 equivalents, more preferably 1.5 equivalents, and particularly preferably 1.1 equivalents.

If the amount of polyisocyanate used is too large, unreacted isocyanate groups will cause side reactions, and the resulting polyurethane will have too high a viscosity, making it difficult to handle and tending to reduce flexibility. If it is too high, the molecular weight of the polyurethane will not be sufficiently large, and sufficient polyurethane strength will not be obtained.
The amount of the chain extender is not particularly limited, but when the number obtained by subtracting the number of isocyanate groups of the polyisocyanate from the total number of hydroxyl groups of the polycarbonate diol of the present invention and other polyols is 1 equivalent, the lower limit is preferably Is 0.7 equivalents, more preferably 0.8 equivalents, still more preferably 0.9 equivalents, particularly preferably 0.95 equivalents, and the upper limit is preferably 3.0 equivalents, more preferably 2.0 equivalents, Preferably it is 1.5 equivalent, Most preferably, it is 1.1 equivalent. If the amount of chain extender used is too large, the resulting polyurethane tends to be difficult to dissolve in the solvent and difficult to process. If too small, the resulting polyurethane is too soft and has sufficient strength, hardness, elastic recovery performance and elasticity. Holding performance may not be obtained or heat resistance may deteriorate.

<2-9. Two-stage method>
The two-stage method is also called a prepolymer method, and mainly includes the following methods.
(A) The polycarbonate diol of the present invention and other polyols and an excess of polyisocyanate are added in advance from an amount in which the reaction equivalent ratio of polyisocyanate / (polycarbonate diol of the present invention and other polyols) exceeds 1 to 10. A method of producing a polyurethane by reacting at 0 or less to produce a prepolymer having a molecular chain terminal at an isocyanate group, and then adding a chain extender thereto (b) in advance polyisocyanate, excess polycarbonate diol and A prepolymer whose molecular chain terminal is a hydroxyl group is produced by reacting with other polyols at a reaction equivalent ratio of polyisocyanate / (polycarbonate diol of the present invention and other polyols) of 0.1 or more and less than 1.0. This is followed by isocyanine as a chain extender. Method for producing a polyurethane polyisocyanate preparative groups reacted.

The two-stage method can be carried out without a solvent or in the presence of a solvent.
The polyurethane production by the two-stage method can be performed by any one of the methods (1) to (3) described below.
(1) Without using a solvent, first, a polyisocyanate, a polycarbonate diol, and a polyol other than that are directly reacted to synthesize a prepolymer and used as it is in a chain extension reaction.
(2) A prepolymer is synthesized by the method of (1), then dissolved in a solvent, and used for the subsequent chain extension reaction.
(3) Using a solvent from the beginning, polyisocyanate, polycarbonate diol and other polyol are reacted, and then chain extension reaction is performed.

In the case of the method (1), in the chain extension reaction, the polyurethane is obtained in the form of coexisting with the solvent by dissolving the chain extender in the solvent or simultaneously dissolving the prepolymer and the chain extender in the solvent. This is very important.
The amount of polyisocyanate used in the method of the two-stage method (a) is not particularly limited, but the lower limit is preferable as the number of isocyanate groups when the number of total hydroxyl groups of polycarbonate diol and other polyols is 1 equivalent. Is an amount exceeding 1.0 equivalent, more preferably 1.2 equivalent, still more preferably 1.5 equivalent, and the upper limit is preferably 10.0 equivalent, more preferably 5.0 equivalent, still more preferably 3.0 equivalent. Equivalent range.

If the amount of isocyanate used is too large, there will be a tendency for excess isocyanate groups to cause side reactions and it will be difficult to reach the desired properties of polyurethane. May be low.
The amount of chain extender used is not particularly limited, but the lower limit is preferably 0.1 equivalents, more preferably 0.5 equivalents, and even more preferably 0 with respect to the number of equivalents of 1 isocyanate group contained in the prepolymer. 0.8 equivalent, and the upper limit is preferably 5.0 equivalents, more preferably 3.0 equivalents, and even more preferably 2.0 equivalents.

When performing the chain extension reaction, monofunctional organic amines or alcohols may coexist for the purpose of adjusting the molecular weight.
The amount of polyisocyanate used in preparing the prepolymer having a terminal hydroxyl group in the two-step method (b) is not particularly limited. As the number of isocyanate groups in the case of equivalent, the lower limit is preferably 0.1 equivalent, more preferably 0.5 equivalent, still more preferably 0.7 equivalent, and the upper limit is preferably 0.99 equivalent, more preferably 0.98 equivalent, more preferably 0.97 equivalent.

If the amount of isocyanate used is too small, the process for obtaining the desired molecular weight in the subsequent chain extension reaction tends to be long and production efficiency tends to decrease.If the amount is too large, the viscosity becomes too high and the flexibility of the polyurethane obtained is too high. In some cases, it may decrease, or the productivity may be inferior due to poor handling.
The amount of chain extender used is not particularly limited, but when the total number of hydroxyl groups of the polycarbonate diol and other polyols used in the prepolymer is 1 equivalent, the total of the isocyanate groups used in the prepolymer is added. As the equivalent, the lower limit is preferably 0.7 equivalents, more preferably 0.8 equivalents, still more preferably 0.9 equivalents, and the upper limit is preferably less than 1.0 equivalents, more preferably 0.99 equivalents, still more preferably. Is in the range of 0.98 equivalents.

When performing the chain extension reaction, monofunctional organic amines or alcohols may coexist for the purpose of adjusting the molecular weight.
The chain extension reaction is usually carried out at 0 ° C. to 250 ° C., but this temperature varies depending on the amount of the solvent, the reactivity of the raw materials used, the reaction equipment, etc., and is not particularly limited. If the temperature is too low, the progress of the reaction may be too slow, or the production time may be prolonged due to the low solubility of the raw materials and polymer, and if it is too high, side reactions and decomposition of the resulting polyurethane may occur. . The chain extension reaction may be performed while degassing under reduced pressure.

Moreover, a catalyst, a stabilizer, etc. can also be added to chain extension reaction as needed.
Examples of the catalyst include compounds such as triethylamine, tributylamine, dibutyltin dilaurate, stannous octylate, acetic acid, phosphoric acid, sulfuric acid, hydrochloric acid, sulfonic acid and the like. You may use the above together. Examples of stabilizers include 2,6-dibutyl-4-methylphenol, distearylthiodipropionate, N, N'-di-2-naphthyl-1,4-phenylenediamine, and tris (dinonylphenyl) phos. A compound such as phyto may be mentioned, and one kind may be used alone, or two or more kinds may be used in combination. In the case where the chain extender is highly reactive such as a short chain aliphatic amine, the reaction may be carried out without adding a catalyst.

<2-10. Water-based polyurethane emulsion>
It is also possible to produce an aqueous polyurethane emulsion using the polycarbonate diol of the present invention.
In that case, when a prepolymer is produced by reacting a polyol containing polycarbonate diol and excess polyisocyanate, a compound having at least one hydrophilic functional group and at least two isocyanate-reactive groups is mixed. A prepolymer is formed, and an aqueous polyurethane emulsion is obtained through a neutralization and chlorination step of hydrophilic functional groups, an emulsification step by adding water, and a chain extension reaction step.

  The hydrophilic functional group of the compound having at least one hydrophilic functional group and at least two isocyanate-reactive groups used here is, for example, a carboxyl group or a sulfonic acid group, and can be neutralized with an alkaline group. It is a basic group. The isocyanate-reactive group is a group that generally reacts with isocyanate to form a urethane bond or a urea bond, such as a hydroxyl group, a primary amino group, or a secondary amino group, and these are mixed in the same molecule. It does not matter.

  Specific examples of the compound having at least one hydrophilic functional group and at least two isocyanate-reactive groups include 2,2′-dimethylolpropionic acid, 2,2-methylolbutyric acid, 2,2 ′. -Dimethylol valeric acid etc. are mentioned. Further, diaminocarboxylic acids such as lysine, cystine, 3,5-diaminocarboxylic acid and the like can also be mentioned. These may be used alone or in combination of two or more. When these are actually used, they are used after neutralizing with an amine such as trimethylamine, triethylamine, tri-n-propylamine, tributylamine or triethanolamine, or an alkaline compound such as sodium hydroxide, potassium hydroxide or ammonia. be able to.

  When an aqueous polyurethane emulsion is produced, the amount of the compound having at least one hydrophilic functional group and at least two isocyanate-reactive groups is used in order to increase the dispersion performance in water. Preferably it is 1 weight% with respect to the total weight of polycarbonate diol and the other polyol, More preferably, it is 5 weight%, More preferably, it is 10 weight%. On the other hand, if too much is added, the properties of the polycarbonate diol of the present invention may not be maintained, so the upper limit is preferably 50% by weight, more preferably 40% by weight, and even more preferably 30% by weight. It is.

In the case of producing an aqueous polyurethane emulsion, it may be reacted in the presence of a solvent such as methyl ethyl ketone, acetone, or N-methyl-2-pyrrolidone in the prepolymer process, or may be allowed to react in the absence of a solvent. Moreover, when using a solvent, after manufacturing an aqueous | water-based emulsion, it is preferable to distill a solvent off by distillation.
In the case of producing an aqueous polyurethane emulsion without using a solvent with the polycarbonate diol of the present invention, the upper limit of the number average molecular weight determined from the hydroxyl value of the polycarbonate diol is preferably 5000, more preferably 4500, and still more preferably 4000. . The lower limit is preferably 300, more preferably 500, and still more preferably 800. When the number average molecular weight obtained from the hydroxyl value exceeds 5000 or is smaller than 300, emulsification may be difficult.

  In addition, in the synthesis or storage of water-based polyurethane emulsions, typical examples include higher fatty acids, resin acids, acidic fatty alcohols, sulfate esters, higher alkyl sulfonates, higher alkyl sulfonates, alkyl aryl sulfonates, sulfonated castor oil, and sulfosuccinate esters. Anionic surfactants, primary surfactants, secondary amine salts, tertiary amine salts, quaternary amine salts, cationic surfactants such as pyridinium salts, or ethylene oxide and long chain fatty alcohols or phenols The emulsion stability may be maintained by using a nonionic surfactant represented by a known reaction product.

In addition, when preparing a water-based polyurethane emulsion, water is mechanically mixed under high shear in the presence of an emulsifier in an organic solvent solution of the prepolymer, if necessary, without a neutralization chlorination step. You can also do it.
The water-based polyurethane emulsion thus produced can be used for various applications. In particular, recently, there has been a demand for chemical raw materials with a small environmental load, and it is possible to replace conventional products for the purpose of using no organic solvent.

  As a specific use of the water-based polyurethane emulsion, for example, use in coating agents, water-based paints, adhesives, synthetic leather, and artificial leather is preferable. In particular, the water-based polyurethane emulsion produced using the polycarbonate diol of the present invention has a structural unit derived from the compound represented by the above formula (B) in the polycarbonate diol, and is therefore flexible and a coating agent. For example, it can be used more effectively than a conventional water-based polyurethane emulsion using a polycarbonate diol.

<2-11. Additives>
The polyurethane of the present invention produced using the polycarbonate diol of the present invention includes a heat stabilizer, a light stabilizer, a colorant, a filler, a stabilizer, an ultraviolet absorber, an antioxidant, an anti-tacking agent, a flame retardant, and aging. Various additives such as an inhibitor and an inorganic filler can be added and mixed as long as the properties of the polyurethane of the present invention are not impaired.

  Compounds that can be used as heat stabilizers include phosphoric acid, phosphorous acid aliphatic, aromatic or alkyl group-substituted aromatic esters and hypophosphorous acid derivatives, phenylphosphonic acid, phenylphosphinic acid, diphenylphosphonic acid, polyphosphonate, dialkyl Phosphorus compounds such as pentaerythritol diphosphite and dialkylbisphenol A diphosphite; phenol derivatives, particularly hindered phenol compounds; thioethers, dithioacid salts, mercaptobenzimidazoles, thiocarbanilides, thiodipropionic acid esters, etc. Compounds containing sulfur; tin compounds such as tin malate and dibutyltin monoxide can be used.

Specific examples of the hindered phenol compound include Irganox 1010 (trade name: manufactured by BASF Japan Ltd.), Irganox 1520 (trade name: manufactured by BASF Japan Ltd.), Irganox 245 (trade name: manufactured by BASF Japan Ltd.), and the like.
Examples of the phosphorus compound include PEP-36, PEP-24G, and HP-10 (all trade names: manufactured by ADEKA Corporation) Irgafos 168 (trade name: manufactured by BASF Japan Corporation).

Specific examples of the compound containing sulfur include thioether compounds such as dilauryl thiopropionate (DLTP) and distearyl thiopropionate (DSTP).
Examples of light stabilizers include benzotriazole-based compounds, benzophenone-based compounds, and the like. Specifically, “TINUVIN622LD”, “TINUVIN765” (above, Ciba
Specialty Chemicals Co., Ltd.), “SANOL LS-2626”, “SANOL LS-765” (Sanyo Co., Ltd.) can be used.

Examples of the ultraviolet absorber include “TINUVIN 328” and “TINUVIN 234” (manufactured by Ciba Specialty Chemicals Co., Ltd.).
Colorants include direct dyes, acid dyes, basic dyes, metal complex dyes and the like; inorganic pigments such as carbon black, titanium oxide, zinc oxide, iron oxide and mica; and coupling azo series, condensed azo series, And organic pigments such as anthraquinone, thioindigo, dioxazone, and phthalocyanine.

Examples of the inorganic filler include short glass fibers, carbon fibers, alumina, talc, graphite, melamine, and clay.
Examples of the flame retardant include addition of phosphorus and halogen-containing organic compounds, bromine or chlorine-containing organic compounds, ammonium polyphosphate, aluminum hydroxide, antimony oxide, and reactive flame retardants.

These additives may be used alone or in combination of two or more in any combination and ratio.
The lower limit of the addition amount of these additives is preferably 0.01% by weight, more preferably 0.05% by weight, still more preferably 0.1% by weight, and the upper limit is preferably 10% by weight with respect to the polyurethane. % By weight, more preferably 5% by weight, still more preferably 1% by weight. If the amount of the additive added is too small, the effect of the addition cannot be sufficiently obtained, and if it is too large, it may precipitate in the polyurethane or generate turbidity.

<2-12. Polyurethane film and polyurethane plate>
When a film is produced using the polyurethane of the present invention, the lower limit of the thickness of the film is preferably 10 μm, more preferably 20 μm, still more preferably 30 μm, and the upper limit is preferably 1000 μm, more preferably 500 μm, still more preferably. Is 100 μm.
If the thickness of the film is too thick, sufficient moisture permeability tends not to be obtained, and if it is too thin, pinholes are generated or the film tends to be blocked and difficult to handle.

<2-13. Molecular weight>
The molecular weight of the polyurethane of the present invention is appropriately adjusted according to its use and is not particularly limited, but is preferably 50,000 to 500,000 as a weight average molecular weight (Mw) in terms of polystyrene measured by GPC. More preferably, it is 10,000 to 300,000. If Mw is smaller than the lower limit, sufficient strength and hardness may not be obtained. If Mw is larger than the upper limit, handling properties such as workability tend to be impaired.

<2-14. Chemical resistance>
For example, the polyurethane of the present invention is evaluated by the method described in the Examples section below, and the change rate (%) ) Is preferably 40% or less, more preferably 30% or less, and even more preferably 20% or less.
If the weight change rate exceeds the upper limit, desired chemical resistance may not be obtained.

<2-15. Oleic acid resistance>
The polyurethane of the present invention is, for example, evaluated by the method described in the Examples section below. (%) Is preferably 80% or less, more preferably 60% or less, further preferably 50% or less, particularly preferably 45% or less, and most preferably 40% or less.
If the weight change rate exceeds the upper limit, sufficient oleic acid resistance may not be obtained.

<2-16. Ethanol resistance>
The polyurethane of the present invention is, for example, evaluated by the method described in the Examples section below, and the change rate (%) of the weight of the polyurethane test piece after being immersed in ethanol relative to the weight of the polyurethane test piece before being immersed in ethanol. ) Is preferably 25% or less, more preferably 23% or less, further preferably 21% or less, particularly preferably 20% or less, and most preferably 19% or less.
If the weight change rate exceeds the upper limit, sufficient ethanol resistance may not be obtained.

<2-17. Tensile breaking elongation>
The polyurethane of the present invention is measured on a strip-shaped sample having a width of 10 mm, a length of 100 mm, and a thickness of about 50 to 100 μm at a temperature of 23 ° C. and a relative humidity of 50% at a chuck distance of 50 mm and a tensile speed of 500 mm / min. The lower limit of the tensile elongation at break is preferably 50%, more preferably 100%, still more preferably 150%, and the upper limit is preferably 900%, more preferably 850%, and still more preferably 800%. If the tensile elongation at break is less than the above lower limit, handling properties such as workability tend to be impaired, and if it exceeds the upper limit, sufficient chemical resistance may not be obtained.

<2-18. Young's modulus>
Using the polycarbonate diol of the present invention, MDI, and 1,4BD, the weight-average molecular weight (Mw) in terms of polystyrene measured by GPC, which is manufactured by a one-step method with an HS content of 12% to 13%, is 140,000. The Young's modulus at 23 ° C. measured by the same method as the above-described measurement of tensile elongation at break of 210,000 polyurethane (hereinafter sometimes referred to as “specific polyurethane”) is preferably 0.02 or more, more preferably It is 0.04 or more, more preferably 0.06 or more. Further, it is preferably 2 or less, more preferably 1 or less, and still more preferably 0.5 or less. If the Young's modulus is too low, chemical resistance may be insufficient. If the Young's modulus is too high, flexibility may be insufficient, and handling properties such as workability may be impaired. Further, the Young's modulus measured by the same method as the above tensile break elongation measurement except that the specific polyurethane is set to −10 ° C. is preferably 0.01 or more, more preferably 0.02 or more, and further preferably 0.03 or more. Especially preferably, it is 0.05 or more. Further, it is preferably 2 or less, more preferably 1 or less, further preferably 0.5 or less, and particularly preferably 0.3 or less. If the Young's modulus at −10 ° C. is less than the above lower limit, chemical resistance may be insufficient. If the Young's modulus at −10 ° C. exceeds the above upper limit, flexibility at low temperatures may be insufficient, and handling properties such as workability may be impaired.

Here, the Young's modulus is a stress value at an elongation of 1% as the slope of the stress value at the initial elongation, and is specifically measured by the method described in the section of Examples described later. .
The HS (hard segment) content% can be calculated by the following equation. HS content (% by weight) = [Polyisocyanate charge weight (g) + Chain extender charge weight (g) + Hardness modifier (g)] ÷ [Polyisocyanate charge weight (g) + Polycarbonate diol charge weight (g) + Other polyol charge weight (g) + chain extender charge weight (g) + hardness modifier (g)]
Each term of the above formula is a numerical value related to the raw material used at the time of urethane production.

<2-19. 100% modulus>
When the polyurethane of the present invention is obtained by reacting 2 equivalents of 4,4′-dicyclohexylmethane diisocyanate with the polycarbonate diol of the present invention and further performing chain extension reaction with isophoronediamine to obtain a polyurethane by a two-stage method, the width is 10 mm, Preferably, the lower limit of 100% modulus measured at a temperature of 23 ° C. and a relative humidity of 50% for a strip-shaped sample having a length of 100 mm and a thickness of about 50 to 100 μm at a chuck distance of 50 mm and a tensile speed of 500 mm / min. It is 0.1 MPa or more, more preferably 0.5 MPa or more, further preferably 1 MPa or more, and the upper limit is preferably 20 MPa or less, more preferably 10 MPa or less, still more preferably 6 MPa or less. If the 100% modulus is less than the above lower limit, chemical resistance may not be sufficient, and if it exceeds the upper limit, flexibility tends to be insufficient or handling properties such as workability tend to be impaired. Furthermore, the 100% modulus at −10 ° C. of the specific polyurethane is preferably 0.5 or more, more preferably 1.0 or more, still more preferably 1.5 or more, and particularly preferably 2.0 or more. Further, it is preferably 13.0 or less, more preferably 12.5 or less, further preferably 12.0 or less, particularly preferably 11.5 or less, and most preferably 10.0 or less. If the 100% modulus at −10 ° C. is less than the above lower limit, chemical resistance may be insufficient. When the 100% modulus at −10 ° C. exceeds the above upper limit, flexibility at low temperatures may be insufficient, and handling properties such as workability may be impaired.

<2-20. Low temperature characteristics>
The polyurethane of the present invention has good low-temperature characteristics. The low-temperature characteristics in this patent can be evaluated by tensile elongation at break, Young's modulus, and 100% modulus in a tensile test at a low temperature such as −10 ° C. Specifically, it refers to flexibility at low temperatures, impact resistance, flex resistance, and durability.

<2-21. Heat resistance>
In the polyurethane of the present invention, a urethane film having a width of 100 mm, a length of 100 mm, and a thickness of about 50 to 100 μm is heated in a gear oven at a temperature of 120 ° C. for 400 hours, and the weight average molecular weight (Mw) of the heated sample is heated. The lower limit is preferably 15% or more, more preferably 20% or more, still more preferably 30% or more, particularly preferably 45% or more, and the upper limit is preferably 120% or less with respect to the previous weight average molecular weight (Mw). More preferably, it is 110% or less, More preferably, it is 105% or less.

<2-22. Glass transition temperature>
When the polycarbonate diol of the present invention is reacted with 2 equivalents of 4,4′-dicyclohexylmethane diisocyanate and further subjected to chain extension reaction with isophoronediamine to obtain a polyurethane by a two-stage method, it is converted to polystyrene measured by GPC. The lower limit of the glass transition temperature (Tg) of the specific polyurethane having a weight average molecular weight (Mw) of 130,000 to 210,000 is preferably −50 ° C., more preferably −45 ° C., further preferably −40 ° C., and the upper limit is preferably Is −20 ° C., more preferably −25 ° C., still more preferably −30 ° C. If Tg is less than the above lower limit, chemical resistance may not be sufficient, and if it exceeds the upper limit, low temperature characteristics may not be sufficient.

<2-23. Application>
The polyurethane of the present invention is excellent in chemical resistance and has good low-temperature characteristics. Therefore, foam, elastomer, elastic fiber, paint, fiber, pressure-sensitive adhesive, adhesive, flooring, sealant, medical material, artificial leather, It can be widely used for synthetic leather, coating agents, water-based polyurethane paints, active energy ray-curable resin compositions, and the like.

In particular, when the polyurethane of the present invention is used for artificial leather, synthetic leather, water-based polyurethane, adhesives, elastic fibers, medical materials, flooring materials, paints, coating agents, etc., the chemical resistance and the low-temperature characteristics are good. Because it has a balance, it is highly durable in areas where it touches human skin and where cosmetic drugs and alcohol for disinfection are used. A good characteristic of being strong can be imparted. Further, it is also suitable for an intermediate coating material for automobile exteriors that require more stringent flexibility at low temperatures.

  The polyurethane of the present invention can be used as a cast polyurethane elastomer. Specific applications include rolling rolls, papermaking rolls, office equipment, rolls such as pre-tension rolls, forklifts, solid tires for automobile vehicles, trams, carts, etc., casters, industrial products such as conveyor belt idlers, guides There are rolls, pulleys, steel pipe linings, ore rubber screens, gears, connection rings, liners, pump impellers, cyclone cones, and cyclone liners. It can also be used for OA equipment belts, paper feed rolls, copying cleaning blades, snow plows, toothed belts, surferers, and the like.

  The polyurethane of the present invention is also applied for use as a thermoplastic elastomer. For example, it can be used for tubes and hoses, spiral tubes, fire hoses, etc. in pneumatic equipment, coating equipment, analytical equipment, physics and chemistry equipment, metering pumps, water treatment equipment, industrial robots and the like used in the food and medical fields. Moreover, it is used for various power transmission mechanisms, spinning machines, packing equipment, printing machines and the like as belts such as round belts, V belts, and flat belts. Also, it can be used for footwear heel tops, shoe soles, couplings, packings, pole joints, bushes, gears, rolls and other equipment parts, sports equipment, leisure goods, watch belts, and the like. Furthermore, examples of automobile parts include oil stoppers, gear boxes, spacers, chassis parts, interior parts, tire chain substitutes, and the like. In addition, it can be used for films such as keyboard films and automobile films, curl cords, cable sheaths, bellows, transport belts, flexible containers, binders, synthetic leather, depinning products, adhesives, and the like.

The polyurethane of the present invention can also be applied as a solvent-based two-component paint, and can be applied to wood products such as musical instruments, Buddhist altars, furniture, decorative plywood, and sports equipment. Moreover, it can be used for automobile repair as tar epoxy urethane.
The polyurethane of the present invention can be used as a component of a moisture-curable one-component paint, a blocked isocyanate solvent paint, an alkyd resin paint, a urethane-modified synthetic resin paint, an ultraviolet curable paint, a water-based urethane paint, etc. Paints for plastic bumpers, strippable paints, coating agents for magnetic tape, floor tiles, flooring materials, overprint varnishes such as paper and wood grain printing films, wood varnishes, coil coats for high processing, optical fiber protective coatings, solder resists, metals It can be applied to a top coat for printing, a base coat for vapor deposition, a white coat for food cans, and the like.

The polyurethane of the present invention can also be applied to food packaging, shoes, footwear, magnetic tape binders, decorative paper, wood, structural members, etc. as adhesives and adhesives, and as low temperature adhesives and hot melt components Can also be used.
The polyurethane of the present invention can be used as a binder for magnetic recording media, inks, castings, fired bricks, graft materials, microcapsules, granular fertilizers, granular agricultural chemicals, polymer cement mortars, resin mortars, rubber chip binders, recycled foams, glass fiber sizing, etc. It can be used.

The polyurethane of the present invention can be used as a component of a fiber processing agent for shrink-proofing, anti-molding, water-repellent processing, and the like.
When the polyurethane of the present invention is used as an elastic fiber, the fiberizing method can be carried out without any limitation as long as it can be spun. For example, a melt spinning method in which the pellets are once pelletized, melted, and directly spun through a spinneret can be employed. When elastic fibers are obtained from the polyurethane of the present invention by melt spinning, the spinning temperature is preferably 250 ° C. or lower, more preferably 2
It is 00 degreeC or more and 235 degrees C or less.

  The polyurethane elastic fiber of the present invention can be used as a bare yarn as it is, or can be coated with another fiber and used as a coated yarn. Examples of other fibers include conventionally known fibers such as polyamide fibers, wool, cotton, and polyester fibers. Among them, polyester fibers are preferably used in the present invention. The polyurethane elastic fiber of the present invention may contain a dyeing type disperse dye.

The polyurethane of the present invention can be used as a sealant caulking for concrete wall, induction joint, sash area, wall PC joint, ALC joint, board joint, composite glass sealant, heat insulation sash sealant, automotive sealant, etc. .
The polyurethane of the present invention can be used as a medical material. As a blood compatible material, a tube, a catheter, an artificial heart, an artificial blood vessel, an artificial valve, etc., and as a disposable material, a catheter, a tube, a bag, and a surgical glove. It can be used for artificial kidney potting materials.
The polyurethane of the present invention can be used as a raw material for UV curable paints, electron beam curable paints, photosensitive resin compositions for flexographic printing plates, photocurable optical fiber coating materials, etc. by modifying the ends. it can.

<2-24. Urethane (meth) acrylate oligomer>
Moreover, a urethane (meth) acrylate oligomer can be produced by addition reaction of polyisocyanate and droxyalkyl (meth) acrylate using the polycarbonate diol of the present invention. When a polyol, which is another raw material compound, and a chain extender are used in combination, the urethane (meth) acrylate oligomer can be produced by addition reaction of these other raw material compounds with polyisocyanate. .

In addition, the charging ratio of each raw material compound at that time is substantially equal to or the same as the composition of the target urethane (meth) acrylate oligomer.
The amount of all isocyanate groups in the urethane (meth) acrylate oligomer and the amount of all functional groups that react with isocyanate groups such as hydroxyl groups and amino groups are usually equimolar in theory.

  When producing urethane (meth) acrylate oligomers, the amount of hydroxyalkyl (meth) acrylate used is determined based on the amount of hydroxyalkyl (meth) acrylate, polycarbonate diol, and other raw material compounds used as needed, and 10 mol% or more, preferably 15 mol% or more, more preferably 25 mol% or more, and usually 70 mol% or less, based on the total amount of the compound containing a functional group that reacts with isocyanate such as a chain extender. The amount is preferably 50 mol% or less. According to this ratio, the molecular weight of the urethane (meth) acrylate oligomer obtained can be controlled. When the proportion of hydroxyalkyl (meth) acrylate is large, the molecular weight of the urethane (meth) acrylate oligomer tends to be small, and when the proportion is small, the molecular weight tends to be large.

  The amount of polycarbonate diol used is preferably 25 mol% or more, more preferably 50 mol% or more, still more preferably 70 mol% or more, based on the total amount of polycarbonate diol and polyol used. When the usage-amount of polycarbonate diol is larger than the said lower limit, there exists a tendency for the hardness and stain resistance of the hardened | cured material obtained to become favorable, and it is preferable.

Further, the amount of polycarbonate diol used is preferably 10% by mass or more, more preferably 30% by mass or more, still more preferably 50% by mass or more, particularly preferably based on the total amount of polycarbonate diol and polyol used. Is 70% by mass or more. If the amount of polycarbonate diol used is greater than the lower limit, the viscosity of the resulting composition will decrease and workability will improve, and the mechanical strength, hardness and abrasion resistance of the resulting cured product will tend to improve. preferable.

  Further, the amount of polycarbonate diol used is preferably 25 mol% or more, more preferably 50 mol% or more, and still more preferably 70 mol% or more with respect to the total amount of polycarbonate diol and polyol used. When the usage-amount of polycarbonate diol is larger than the said lower limit, it will become the tendency for the elongation of a hardened | cured material obtained and a weather resistance to improve, and is preferable.

  Furthermore, when a chain extender is used, the amount of polyol used is preferably 70 mol% or more, more preferably 80 mol%, based on the total amount of compounds used in combination of polycarbonate diol and polyol and chain extender. The mol% or more, more preferably 90 mol% or more, particularly preferably 95 mol% or more. When the amount of polyol is larger than the above lower limit value, the liquid stability tends to be improved, which is preferable.

  In the production of the urethane (meth) acrylate oligomer, a solvent can be used for the purpose of adjusting the viscosity. A solvent may be used individually by 1 type and may be used in mixture of 2 or more types. As the solvent, any known solvent can be used. Preferable solvents include toluene, xylene, ethyl acetate, butyl acetate, cyclohexanone, methyl ethyl ketone, and methyl isobutyl ketone. The solvent can be used usually at less than 300 parts by mass with respect to 100 parts by mass of the solid content in the reaction system.

  In the production of the urethane (meth) acrylate oligomer, the total content of the urethane (meth) acrylate oligomer to be produced and the raw material compounds thereof is preferably 20% by mass or more, based on the total amount of the reaction system, and 40% by mass. % Or more is more preferable. In addition, the upper limit of this total content is 100 mass%. It is preferable for the total content of the urethane (meth) acrylate oligomer and its raw material compound to be 20% by mass or more because the reaction rate tends to increase and the production efficiency tends to improve.

  An addition reaction catalyst can be used in the production of the urethane (meth) acrylate oligomer. Examples of the addition reaction catalyst include dibutyltin laurate, dibutyltin dioctoate, dioctyltin dilaurate, and dioctyltin dioctoate. An addition reaction catalyst may be used individually by 1 type, and 2 or more types may be mixed and used for it. Of these, the addition reaction catalyst is preferably dioctyltin dilaurate from the viewpoints of environmental adaptability, catalytic activity, and storage stability.

The addition reaction catalyst has an upper limit of usually 1000 ppm or less, preferably 500 ppm or less, and a lower limit of usually 10 ppm or more, preferably 30 ppm or more, with respect to the total content of the urethane (meth) acrylate oligomer to be produced and its raw material compounds. Used.
Moreover, a polymerization inhibitor can be used together when the reaction system contains a (meth) acryloyl group during the production of the urethane (meth) acrylate oligomer. Examples of such polymerization inhibitors include phenols such as hydroquinone, methylhydroquinone, hydroquinone monoethyl ether, dibutylhydroxytoluene, amines such as phenothiazine and diphenylamine, copper salts such as copper dibutyldithiocarbamate, and manganese such as manganese acetate. Examples thereof include salts, nitro compounds, and nitroso compounds. A polymerization inhibitor may be used individually by 1 type, and 2 or more types may be mixed and used for it. Of these, phenols are preferable as the polymerization inhibitor.

The polymerization inhibitor has an upper limit of usually 3000 ppm or less, preferably 1000 ppm or less, particularly preferably 500 ppm or less, and a lower limit usually based on the total content of the urethane (meth) acrylate oligomer and raw material compounds to be produced. It is used at 50 ppm or more, preferably 100 ppm or more.
During the production of the urethane (meth) acrylate oligomer, the reaction temperature is usually 20 ° C. or higher, preferably 40 ° C. or higher, and more preferably 60 ° C. or higher. A reaction temperature of 20 ° C. or higher is preferable because the reaction rate increases and the production efficiency tends to improve. Moreover, reaction temperature is 120 degrees C or less normally, and it is preferable that it is 100 degrees C or less. A reaction temperature of 120 ° C. or lower is preferable because side reactions such as an allohanato reaction are less likely to occur. When the reaction system contains a solvent, the reaction temperature is preferably lower than the boiling point of the solvent. When (meth) acrylate is contained, the reaction temperature is 70 ° C. from the viewpoint of preventing the reaction of the (meth) acryloyl group. The following is preferable. The reaction time is usually about 5 to 20 hours.

  The number average molecular weight of the urethane (meth) acrylate oligomer thus obtained is preferably 500 or more, particularly preferably 1000 or more, preferably 10,000 or less, particularly 5000 or less, especially 3000 or less. When the number average molecular weight of the urethane (meth) acrylate oligomer is not less than the above lower limit, the resulting cured film has good three-dimensional workability and tends to have an excellent balance between three-dimensional workability and stain resistance. When the number average molecular weight of the urethane (meth) acrylate oligomer is not more than the above upper limit, the cured film obtained from the composition has good contamination resistance and tends to have a good balance between three-dimensional processability and contamination resistance. Therefore, it is preferable. This is because the three-dimensional workability and stain resistance depend on the distance between the cross-linking points in the network structure, and as this distance increases, the structure becomes flexible and easily stretched, and the three-dimensional workability is superior. This is presumed to be because the structure becomes a strong structure and is excellent in stain resistance.

<2-25. Polyester elastomer>
Furthermore, the polycarbonate diol of the present invention can be used as a polyester elastomer. The polyester elastomer is a copolymer composed of a hard segment mainly composed of aromatic polyester and a soft segment mainly composed of aliphatic polyether, aliphatic polyester or aliphatic polycarbonate. When the polycarbonate diol of the present invention is used as a constituent component of the soft segment, physical properties such as heat resistance and water resistance are excellent as compared with the case where aliphatic polyether or aliphatic polyester is used. Compared with known polycarbonate diol, it has a meltability, that is, a polycarbonate ester elastomer with a melt flow rate suitable for blow molding and extrusion molding and excellent balance with mechanical strength and other physical properties. It can be suitably used for various molding materials including fibers, films and sheets, for example, molding materials such as elastic yarns and boots, gears, tubes and packings. Specifically, it can be effectively applied to applications such as joint boots such as automobiles and home appliance parts that require heat resistance and durability, and wire covering materials.

<2-26. Active energy ray-curable polymer composition>
Below, the active energy ray-curable polymer composition of the present invention containing the above-mentioned urethane (meth) acrylate oligomer will be described.
The active energy ray-curable polymer composition of the present invention preferably has a molecular weight between calculated network crosslinking points of 500 to 10,000.

In the present specification, the molecular weight between calculated network cross-linking points of the composition is the average molecular weight between active energy ray reactive groups (hereinafter sometimes referred to as “cross-linking points”) that form a network structure in the entire composition. Represents a value. The molecular weight between the calculated network cross-linking points is correlated with the network area at the time of network structure formation,
The crosslink density decreases as the molecular weight between the calculated network crosslink points increases. In the reaction by active energy ray curing, when a compound having only one active energy ray reactive group (hereinafter, sometimes referred to as “monofunctional compound”) reacts, it becomes a linear polymer, while the active energy A network structure is formed when a compound having two or more linear reactive groups (hereinafter sometimes referred to as “polyfunctional compound”) reacts.

  Therefore, the active energy ray reactive group of the polyfunctional compound is a crosslinking point, and the calculation of the molecular weight between the calculated network crosslinking points is centered on the polyfunctional compound having the crosslinking point, and the monofunctional compound has the polyfunctional compound. The molecular weight between the crosslinking points is treated as having an effect of extending the molecular weight, and the molecular weight between the calculation network crosslinking points is calculated. In addition, the calculation of the molecular weight between the calculation network crosslinking points is performed on the assumption that all the active energy ray reactive groups have the same reactivity and that all the active energy ray reactive groups react by irradiation with the active energy ray. .

In a polyfunctional compound single-system composition in which only one type of polyfunctional compound reacts, the molecular weight between the calculated network crosslinking points is twice the average molecular weight per active energy ray reactive group of the polyfunctional compound. . For example, (1000/2) × 2 = 1000 for a bifunctional compound with a molecular weight of 1,000, and (300/3) × 2 = 200 for a trifunctional compound with a molecular weight of 300.
In a polyfunctional compound mixed system composition in which multiple types of polyfunctional compounds react, the average value of the molecular weights between the calculated network cross-linking points of each of the single systems with respect to the total number of active energy ray reactive groups contained in the composition is It is the molecular weight between the calculated network crosslinking points of the composition. For example, in a composition comprising a mixture of 4 moles of a bifunctional compound having a molecular weight of 1,000 and 4 moles of a trifunctional compound having a molecular weight of 300, the total number of reactive energy ray reactive groups in the composition is 2 × 4 + 3 × 4 = 20. The molecular weight between calculated network crosslinking points of the composition is {(1000/2) × 8 + (300/3) × 12} × 2/20 = 520.

  When a monofunctional compound is included in the composition, a molecule formed by calculation and equimolar to the active energy ray reactive group (that is, the crosslinking point) of the polyfunctional compound, and the monofunctional compound linked to the crosslinking point Assuming that the reaction takes place in the middle of the chain, the extension of the molecular chain by the monofunctional compound at one crosslinking point is the total molecular weight of the monofunctional compound, and the total active energy ray reaction of the polyfunctional compound in the composition. Half of the value divided by the radix. Here, since the molecular weight between the calculated network cross-linking points is considered to be twice the average molecular weight per cross-linking point, the amount extended by the monofunctional compound relative to the calculated molecular weight between the cross-linking points calculated for the polyfunctional compound is The value obtained by dividing the total molecular weight of the monofunctional compound by the total number of reactive energy ray reactive groups of the polyfunctional compound in the composition.

For example, in a composition comprising a mixture of 40 mol of a monofunctional compound having a molecular weight of 100 and 4 mol of a bifunctional compound having a molecular weight of 1,000, the number of reactive energy ray reactive groups of the polyfunctional compound is 2 × 4 = 8. The extension due to the monofunctional compound in the molecular weight between the calculated network cross-linking points is 100 × 40/8 = 500. That is, the molecular weight between calculated network crosslinks of the composition is 1000 + 500 = 1500.
From the above, in the mixture of the monofunctional compound MA mole with molecular weight WA, the fB functional compound MB mole with molecular weight WB, and the fC functional compound MC mole with molecular weight WC, the molecular weight between the calculated network crosslinking points of the composition Can be expressed by the following formula.

  The molecular weight between the calculated network crosslinking points of the active energy ray-curable polymer composition of the present invention calculated in this way is preferably 500 or more, more preferably 800 or more, and 1,000 or more. More preferably, it is preferably 10,000 or less, more preferably 8,000 or less, further preferably 6,000 or less, and even more preferably 4,000 or less. 3,000 or less is particularly preferable.

  A molecular weight between calculated network crosslinking points of 10,000 or less is preferable because the cured film obtained from the composition has good stain resistance and tends to have a good balance between three-dimensional processability and stain resistance. Moreover, it is preferable that the molecular weight between the calculation network cross-linking points is 500 or more because the obtained cured film has good three-dimensional workability and tends to have an excellent balance between the three-dimensional workability and the stain resistance. This is because the three-dimensional workability and stain resistance depend on the distance between the cross-linking points in the network structure. When this distance is increased, the structure becomes flexible and easily stretched, and the three-dimensional processability is excellent. This is presumed to be because the structure becomes a strong structure and is excellent in stain resistance.

The active energy ray-curable polymer composition of the present invention may further contain components other than the urethane (meth) acrylate oligomer. Examples of such other components include an active energy ray-reactive monomer, an active energy ray-curable oligomer, a polymerization initiator, a photosensitizer, an additive, and a solvent.
In the active energy ray-curable polymer composition of the present invention, the content of the urethane (meth) acrylate oligomer is 40% by mass or more based on the total amount of the active energy ray-reactive components including the urethane (meth) acrylate oligomer. It is preferable that it is 60 mass% or more. In addition, the upper limit of this content is 100 mass%. When the content of the urethane (meth) acrylate oligomer is 40% by mass or more, the curability is good and the three-dimensional workability tends to be improved without excessively increasing the mechanical strength of the cured product. This is preferable.

  Moreover, in the active energy ray-curable polymer composition of the present invention, the content of the urethane (meth) acrylate oligomer is preferably large in terms of elongation and film-forming property, and on the other hand, the viscosity is reduced. In terms of points, a smaller number is preferable. From such a viewpoint, the content of the urethane (meth) acrylate oligomer is preferably 50% by mass or more based on the total amount of all components including other components in addition to the active energy ray-reactive component. 70% by mass or more is more preferable. In addition, the upper limit of content of a urethane (meth) acrylate type oligomer is 100 mass%, and it is preferable that this content is less than that.

Moreover, in the active energy ray-curable polymer composition of the present invention, the content of the total amount of the active energy ray-reactive component including the urethane (meth) acrylate oligomer depends on the curing rate and surface curability of the composition. From the standpoint of excellent and no tack remaining, it is preferably 60% by mass or more, more preferably 80% by mass or more, and still more preferably 90% by mass or more based on the total amount of the composition. More preferably, it is 95% by mass or more. In addition, the upper limit of this content is 100 mass%.

  Any known active energy ray-reactive monomer can be used as the active energy ray-reactive monomer. These active energy ray reactive monomers are used for the purpose of adjusting the hydrophilicity / hydrophobicity of urethane (meth) acrylate oligomers and the physical properties such as hardness and elongation of the cured product when the resulting composition is cured. Is done. An active energy ray reactive monomer may be used individually by 1 type, and 2 or more types may be mixed and used for it.

Examples of such active energy ray reactive monomers include vinyl ethers, (meth) acrylamides, and (meth) acrylates. Specific examples include styrene, α-methylstyrene, α-chlorostyrene. Aromatic vinyl monomers such as vinyltoluene and divinylbenzene; vinyl such as vinyl acetate, vinyl butyrate, N-vinylformamide, N-vinylacetamide, N-vinyl-2-pyrrolidone, N-vinylcaprolactam and divinyl adipate Ester monomers; Vinyl ethers such as ethyl vinyl ether and phenyl vinyl ether; Allyl compounds such as diallyl phthalate, trimethylolpropane diallyl ether, and allyl glycidyl ether; (meth) acrylamide, N, N-dimethylacrylamide N, N-dimethylmethacrylamide, N-methylol (meth) acrylamide, N-methoxymethyl (meth) acrylamide, N-butoxymethyl (meth) acrylamide, Nt-butyl (meth) acrylamide, (meth) acryloylmorpholine (Meth) acrylamides such as methylenebis (meth) acrylamide; (meth) acrylic acid, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, (meth) acrylate-n-butyl , (Meth) acrylic acid-i-butyl, (meth) acrylic acid-t-butyl, (meth) acrylic acid hexyl, (meth) acrylic acid-2-ethylhexyl, (meth) acrylic acid lauryl, (meth) acrylic acid Stearyl, tetrahydrofurfuryl (meth) acrylate, (meth) a Morpholyl laurate, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, glycidyl (meth) acrylate, dimethyl (meth) acrylate Aminoethyl, diethylaminoethyl (meth) acrylate, benzyl (meth) acrylate, cyclohexyl (meth) acrylate, phenoxyethyl (meth) acrylate, tricyclodecane (meth) acrylate, dicyclopentenyl (meth) acrylate , (Meth) acrylic acid dicyclopentenyloxyethyl, (meth) acrylic acid dicyclopentanyl, (meth) acrylic acid allyl, (meth) acrylic acid-2-ethoxyethyl, (meth) acrylic acid isobornyl, (meth) Monofunctional (meth) acrylic acid such as phenyl acrylate And ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate ( n = 5-14), propylene glycol di (meth) acrylate, dipropylene glycol di (meth) acrylate, tripropylene glycol di (meth) acrylate, tetrapropylene glycol di (meth) acrylate, di (meth) Polypropylene glycol acrylate (n = 5-14), di (meth) acrylic acid-1,3-butylene glycol, di (meth) acrylic acid-1,4-butanediol, di (meth) acrylic acid polybutylene glycol ( n = 3-16), di (meth) acrylic acid poly Li (1-methylbutylene glycol) (n = 5-20), di (meth) acrylic acid-1,6-hexanediol, di (meth) acrylic acid-1,9-nonanediol, di (meth) acrylic acid Neopentyl glycol, hydroxypivalate neopentyl glycol di (meth) acrylate, di (meth) acrylate dicyclopentanediol, di (meth) acrylate tricyclodecane, trimethylolpropane tri (meth) acrylate, pentaerythritol Tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, ditrimethylolpropane tetra (meth) acrylate, dipentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hex (Meth) acrylate,
Trimethylolpropane trioxyethyl (meth) acrylate, trimethylolpropane trioxypropyl (meth) acrylate, trimethylolpropane polyoxyethyl (meth) acrylate, trimethylolpropane polyoxypropyl (meth) acrylate, tris (2-hydroxyethyl) ) Isocyanurate tri (meth) acrylate, tris (2-hydroxyethyl) isocyanurate di (meth) acrylate, ethylene oxide-added bisphenol A di (meth) acrylate, ethylene oxide-added bisphenol F di (meth) acrylate, propylene oxide-added bisphenol A di (meth) acrylate, propylene oxide-added bisphenol F di (meth) acrylate, tricyclodecane dimethanol (Meth) acrylate, bisphenol A epoxy di (meth) acrylate, polyfunctional (meth) acrylates such as bisphenol F epoxy di (meth) acrylate; and the like.

  Among these, (meth) acryloylmorpholine, (meth) acrylic acid tetrahydrofurfuryl, (meth) acrylic acid benzyl, (meth) acrylic acid cyclohexyl, (meth) acrylic acid, especially in applications where coating properties are required. Has a ring structure in the molecule, such as trimethylcyclohexyl, phenoxyethyl (meth) acrylate, tricyclodecane (meth) acrylate, dicyclopentenyl (meth) acrylate, isobornyl (meth) acrylate, (meth) acrylamide, etc. Monofunctional (meth) acrylates are preferred. On the other hand, in applications where mechanical strength of the resulting cured product is required, di (meth) acrylic acid-1,4-butanediol, di (meth) acrylic acid-1, 6-hexanediol, di (meth) acrylic acid-1,9-nonanediol, di (meth) Neopentyl glycol acrylate, tricyclodecane di (meth) acrylate, trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol tetra (meth) acrylate, Polyfunctional (meth) acrylates such as dipentaerythritol penta (meth) acrylate and dipentaerythritol hexa (meth) acrylate are preferred.

  In the active energy ray-curable polymer composition of the present invention, the content of the active energy ray-reactive monomer is selected from the viewpoints of adjusting the viscosity of the composition and adjusting physical properties such as hardness and elongation of the resulting cured product. It is preferably 50% by mass or less, more preferably 30% by mass or less, still more preferably 20% by mass or less, and still more preferably 10% by mass or less, based on the total amount of the composition. .

The active energy ray-curable oligomer may be used alone or in combination of two or more. Examples of the active energy ray-curable oligomer include epoxy (meth) acrylate oligomers and acrylic (meth) acrylate oligomers.
In the active energy ray-curable polymer composition of the present invention, the content of the active energy ray-reactive oligomer is based on the total amount of the composition from the viewpoint of adjusting physical properties such as hardness and elongation of the obtained cured product. 50% by mass or less, more preferably 30% by mass or less, further preferably 20% by mass or less, and further more preferably 10% by mass or less.

  The polymerization initiator is mainly used for the purpose of improving the initiation efficiency of a polymerization reaction that proceeds by irradiation with active energy rays such as ultraviolet rays and electron beams. As the polymerization initiator, a photoradical polymerization initiator which is a compound having a property of generating radicals by light is generally used, and any known photoradical polymerization initiator can be used. A polymerization initiator may be used individually by 1 type, and 2 or more types may be mixed and used for it. Furthermore, you may use together radical photopolymerization initiator and a photosensitizer.

  Examples of the photo radical polymerization initiator include benzophenone, 2,4,6-trimethylbenzophenone, 4,4-bis (diethylamino) benzophenone, 4-phenylbenzophenone, methylorthobenzoylbenzoate, thioxanthone, diethylthioxanthone, isopropylthioxanthone, chloro Thioxanthone, 2-ethylanthraquinone, t-butylanthraquinone, diethoxyacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, benzyldimethyl ketal, 1-hydroxycyclohexyl phenyl ketone, benzoin methyl ether, benzoin ethyl Ether, benzoin isopropyl ether, benzoin isobutyl ether, methylbenzoylformate, 2-methyl-1- [4- ( Tilthio) phenyl] -2-morpholinopropan-1-one, 2,6-dimethylbenzoyldiphenylphosphine oxide, 2,4,6-trimethylbenzoyldiphenylphosphine oxide, bis (2,6-dimethoxybenzoyl) -2,4 4-trimethylpentylphosphine oxide, bis (2,4,6-trimethylbenzoyl) phenylphosphine oxide, and 2-hydroxy-1- [4- [4- (2-hydroxy-2-methyl-propionyl) -benzyl]- Phenyl] -2-methyl-propan-1-one and the like.

  Among these, benzophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-hydroxycyclohexyl phenyl ketone, 2,4,6, since the curing speed is high and the crosslinking density can be sufficiently increased. -Trimethylbenzoyldiphenylphosphine oxide and 2-hydroxy-1- [4- [4- (2-hydroxy-2-methyl-propionyl) -benzyl] -phenyl] -2-methyl-propan-1-one 1-hydroxycyclohexyl phenyl ketone, 2,4,6-trimethylbenzoyldiphenylphosphine oxide, and 2-hydroxy-1- [4- [4- (2-hydroxy-2-methyl-propionyl) -benzyl] -phenyl ] 2-Methyl-propan-1-one is more preferred.

In addition, when the active energy ray-curable polymer composition contains a compound having a cationic polymerizable group such as an epoxy group together with a radical polymerizable group, as a polymerization initiator, a photocation together with the above-mentioned photo radical polymerization initiator. A polymerization initiator may be included. Any known cationic photopolymerization initiator can be used.
The content of these polymerization initiators in the active energy ray-curable polymer composition of the present invention is preferably 10 parts by mass or less with respect to a total of 100 parts by mass of the active energy ray-reactive components, More preferably, it is 5 parts by mass or less. When the content of the photopolymerization initiator is 10 parts by mass or less, the mechanical strength is not easily lowered by the initiator decomposition product, which is preferable.

  The photosensitizer can be used for the same purpose as the polymerization initiator. A photosensitizer may be used individually by 1 type and may be used in mixture of 2 or more types. As the photosensitizer, any known photosensitizer can be used as long as the effects of the present invention are obtained. Examples of such photosensitizers include ethanolamine, diethanolamine, triethanolamine, N-methyldiethanolamine, methyl 4-dimethylaminobenzoate, ethyl 4-dimethylaminobenzoate, amyl 4-dimethylaminobenzoate, And 4-dimethylaminoacetophenone.

In the active energy ray-curable polymer composition of the present invention, the content of the photosensitizer is preferably 10 parts by mass or less with respect to 100 parts by mass in total of the active energy ray reactive components. More preferably, it is 5 parts by mass or less. It is preferable for the content of the photosensitizer to be 10 parts by mass or less because it is difficult for mechanical strength to decrease due to a decrease in crosslink density.
The additive is optional, and various materials added to a composition used for the same application can be used as the additive. An additive may be used individually by 1 type, and 2 or more types may be mixed and used for it. Examples of such additives include glass fiber, glass beads, silica, alumina, calcium carbonate, mica, zinc oxide, titanium oxide, mica, talc, kaolin, metal oxide, metal fiber, iron, lead, and metal powder. Fillers such as carbon fibers, carbon black, graphite, carbon nanotubes, carbon materials such as fullerenes such as C60 (fillers and carbon materials may be collectively referred to as “inorganic components”); Agent, heat stabilizer, UV absorber, HALS (hindered amine light stabilizer), anti-fingerprint agent, surface hydrophilizing agent, antistatic agent, slipperiness imparting agent, plasticizer, mold release agent, antifoaming agent, leveling agent, Anti-settling agents, surfactants, thixotropy imparting agents, lubricants, flame retardants, flame retardant aids, polymerization inhibitors, fillers, silane coupling agents and other modifiers; pigments, dyes, hue adjustments Colorants and the like; and, monomer and / or oligomer thereof, or a curing agent required for the synthesis of inorganic components, catalysts, curing accelerators like; and the like.

In the active energy ray-curable polymer composition of the present invention, the content of the additive is preferably 10 parts by mass or less with respect to 100 parts by mass in total of the active energy ray reactive components. It is more preferable that the amount is not more than part by mass. It is preferable for the content of the additive to be 10 parts by mass or less, since it is difficult for mechanical strength to decrease due to a decrease in crosslink density.
The solvent is used for the purpose of adjusting the viscosity of the active energy ray-curable polymer composition of the present invention, for example, depending on the coating method for forming the coating film of the active energy ray-curable polymer composition of the present invention. Can be used. A solvent may be used individually by 1 type and may be used in mixture of 2 or more types. As the solvent, any known solvent can be used as long as the effects of the present invention are obtained. Preferable solvents include toluene, xylene, ethyl acetate, butyl acetate, isopropanol, isobutanol, cyclohexanone, methyl ethyl ketone, and methyl isobutyl ketone. A solvent can be normally used in less than 200 mass parts with respect to 100 mass parts of solid content of an active energy ray curable polymer composition.

  There are no particular limitations on the method of incorporating the active energy ray-curable polymer composition of the present invention into optional components such as the aforementioned additives, and examples thereof include conventionally known mixing and dispersion methods. In addition, in order to disperse | distribute the said arbitrary component more reliably, it is preferable to perform a dispersion | distribution process using a disperser. Specifically, for example, two rolls, three rolls, bead mill, ball mill, sand mill, pebble mill, tron mill, sand grinder, seg barrier striker, planetary stirrer, high speed impeller disperser, high speed stone mill, high speed impact mill , A kneader, a homogenizer, an ultrasonic disperser and the like.

  The viscosity of the active energy ray-curable polymer composition of the present invention can be appropriately adjusted according to the use and usage of the composition, but the viewpoints of handleability, coatability, moldability, three-dimensional formability, etc. From the above, the viscosity at 25 ° C. in an E-type viscometer (rotor 1 ° 34 ′ × R24) is preferably 10 mPa · s or more, more preferably 100 mPa · s or more, 000 mPa · s or less is preferable, and 50,000 mPa · s or less is more preferable. The viscosity of the active energy ray-curable polymer composition can be adjusted by, for example, the content of the urethane (meth) acrylate oligomer of the present invention, the type of the optional component, the blending ratio thereof, and the like.

  As a coating method of the active energy ray-curable polymer composition of the present invention, a bar coater method, an applicator method, a curtain flow coater method, a roll coater method, a spray method, a gravure coater method, a comma coater method, a reverse roll coater method Known methods such as a lip coater method, a die coater method, a slot die coater method, an air knife coater method and a dip coater method can be applied. Among them, a bar coater method and a gravure coater method are preferable.

<2-27. Cured film and laminate>
The active energy ray-curable polymer composition of the present invention can be made into a cured film by irradiating this with active energy rays.
As the active energy rays used when the composition is cured, infrared rays, visible rays, ultraviolet rays, X-rays, electron beams, α rays, β rays, γ rays and the like can be used. From the viewpoint of equipment cost and productivity, it is preferable to use an electron beam or an ultraviolet ray. As a light source, an electron beam irradiation apparatus, an ultrahigh pressure mercury lamp, a high pressure mercury lamp, a medium pressure mercury lamp, a low pressure mercury lamp, a metal halide lamp, Ar A laser, a He—Cd laser, a solid laser, a xenon lamp, a high frequency induction mercury lamp, sunlight, or the like is suitable.

  The irradiation amount of the active energy ray can be appropriately selected according to the type of the active energy ray. For example, when curing is performed by electron beam irradiation, the irradiation amount is preferably 1 to 10 Mrad. In the case of ultraviolet irradiation, it is preferably 50 to 1,000 mJ / cm 2. The atmosphere during curing may be air, an inert gas such as nitrogen or argon. Moreover, you may irradiate in the sealed space between a film or glass, and a metal metal mold | die.

  The thickness of the cured film is appropriately determined according to the intended use, but the lower limit is preferably 1 μm, more preferably 3 μm, and particularly preferably 5 μm. The upper limit is preferably 200 μm, more preferably 100 μm, particularly preferably 50 μm. When the film thickness is 1 μm or more, the design properties and functionality after three-dimensional processing are improved, and when it is 200 μm or less, the internal curability and the three-dimensional workability are preferable. In industrial use, the lower limit is preferably 1 μm, and the upper limit is preferably 100 μm, more preferably 50 μm, particularly preferably 20 μm, and most preferably 10 μm.

A laminate having a layer made of the above cured film can be obtained on a substrate.
The laminate is not particularly limited as long as it has a layer made of a cured film, and may have a layer other than the base material and the cured film between the base material and the cured film, or may be present outside the layer. You may do it. Moreover, the said laminated body may have multiple layers of a base material and a cured film.
As a method of obtaining a laminate having a multi-layer cured film, all layers are laminated in an uncured state and then cured with active energy rays, and the lower layer is cured with active energy rays or semi-cured. Apply a known method such as applying the upper layer and curing again with active energy rays, or applying each layer to the release film or base film and then laminating the layers in an uncured or semi-cured state. Although possible, a method of curing with an active energy ray after laminating in an uncured state is preferable from the viewpoint of improving adhesion between layers. As a method of laminating in an uncured state, a known method such as sequential coating in which the upper layer is applied after the lower layer is applied or simultaneous multilayer coating in which two or more layers are simultaneously applied from multiple slits is applied. Yes, but not always.

Examples of the base material include various shapes such as polyesters such as polyethylene terephthalate and polybutylene terephthalate, polyolefins such as polypropylene and polyethylene, various plastics such as nylon, polycarbonate, (meth) acrylic resin, and plates formed of metal. The article is mentioned.
The cured film can be a film excellent in stain resistance and hardness against general household contaminants such as ink and ethanol, and the laminate using the cured film as a coating on various substrates has a design property and surface. It can be excellent in protection.

In addition, the active energy ray-curable polymer composition of the present invention is flexible, capable of following deformation during three-dimensional processing, considering the molecular weight between the calculation network crosslinking points, elongation at break, mechanical strength, contamination resistance. A cured film having both properties and hardness can be provided.
Moreover, it is expected that the active energy ray-curable polymer composition of the present invention can easily produce a thin film-like resin sheet by applying a single layer.

The breaking elongation of the cured film was determined by cutting the cured film into a width of 10 mm and using a Tensilon tensile tester (Orientec, Tensilon UTM-III-100) at a temperature of 23 ° C., a tensile speed of 50 mm / min, and between chucks. The value measured by performing a tensile test under the condition of a distance of 50 mm is preferably 50% or more, more preferably 75% or more, further preferably 100% or more, and 120% or more. It is particularly preferred.
The cured film and the laminate can be used as a coating substitute film, and can be effectively applied to, for example, interior / exterior building materials, various members of automobiles, home appliances, and the like.

EXAMPLES Hereinafter, although an Example and a comparative example are given and this invention is demonstrated further more concretely, this invention is not limited to these Examples, unless the summary is exceeded.
Below, the evaluation method of each physical property value is as follows.

[Evaluation method: Polycarbonate diol]
<Quantification of phenoxy group content, dihydroxy compound content and phenol content>
Polycarbonate diol was dissolved in CDCl ₃ , 400 MHz ¹ H-NMR (AL-400 manufactured by JEOL Ltd.) was measured, phenoxy group, dihydroxy compound and phenol were identified from the signal position of each component, and each of the integral values was determined from the integral value. The content of was calculated. In this case, the detection limit is 100 ppm as the weight of phenol with respect to the weight of the whole sample, and the compound represented by the formula (A) and the dihydroxy compound such as the compound represented by the formula (B) are 0.1% by weight. is there. The ratio of the phenoxy group is determined from the ratio of the integral value of one proton of the phenoxy group to the integral value of one proton of the whole terminal, and the detection limit of the phenoxy group is 0.05% with respect to the whole terminal. .

<Hydroxyl value>
Based on JIS K1557-1 (2007), the hydroxyl value of polycarbonate diol was measured by a method using an acetylating reagent.
<Measurement of APHA value>
According to JIS K0071-1 (1998), the APHA value was measured in comparison with a standard solution in which a polycarbonate diol was placed in a colorimetric tube. As a reagent, a chromaticity standard solution of 1000 degrees (1 mg Pt / mL) (Kishida Chemical) was used.

<Measurement of melt viscosity>
After the polycarbonate diol was heated to 80 ° C. and melted, the melt viscosity was measured at 80 ° C. using an E-type viscometer (BROOKFIELD DV-II + Pro, Cone: CPE-52).

<Measurement of glass transition temperature (Tg), melting peak temperature, heat of fusion>
About 10 mg of polycarbonate diol is enclosed in an aluminum pan, EXSTAR
Using DSC6200 (manufactured by Seiko Instruments Inc.), in a nitrogen atmosphere at a rate of 20 ° C / min, 30 ° C to 150 ° C, at a rate of 40 ° C / min, 150 ° C to -120 ° C, at a rate of 20 ° C / min The temperature was raised and lowered from −120 ° C. to 120 ° C., the inflection point at the second temperature increase was the glass transition temperature (Tg), and the melting peak temperature and the heat of fusion were determined from the melting peak.

<Molar ratio of dihydroxy compound after hydrolysis>
About 0.5 g of polycarbonate diol was precisely weighed and placed in a 100 mL Erlenmeyer flask, and 5 mL of tetrahydrofuran was added and dissolved. Next, 45 mL of methanol and 5 mL of a 25 wt% aqueous sodium hydroxide solution were added. A condenser was set in a 100 mL Erlenmeyer flask and heated in a water bath at 75 to 80 ° C. for 30 minutes for hydrolysis. 6N after cooling at room temperature
Hydrochloric acid (5 mL) was added to neutralize the sodium hydroxide to bring the pH to 7. The entire amount was transferred to a 100 mL volumetric flask, the inside of the Erlenmeyer flask was washed twice with an appropriate amount of methanol, and the washing solution was also transferred to the 100 mL volumetric flask. After adding an appropriate amount of methanol to 100 mL, the liquid was mixed in a volumetric flask. The supernatant was collected, filtered through a filter, and analyzed by gas chromatography (GC). For the concentration of each dihydroxy compound, a calibration curve was prepared in advance from each known dihydroxy compound as a standard substance, and the weight percentage was calculated from the area ratio obtained by gas chromatography (GC).

(Analysis conditions)
Apparatus: Agilent 6850 (manufactured by Agilent Technologies)
Column: Agilent J & W GC column DB-WAX
Inner diameter 0.25mm, length 60m, membrane pressure 0.25mm
Detector: Hydrogen flame ionization detector (FID)
Temperature rising program: 150 ° C. (2 minutes), 150 ° C. → 280 ° C. (10 ° C./min, 9 minutes),
240 ° C (10 minutes)
The molar ratio of the dihydroxy compound was calculated from the weight% obtained by gas chromatography and the molecular weight of each dihydroxy compound.

[Evaluation method: Polyurethane]
<Isocyanate group concentration measurement>
After diluting 20 mL of a mixed solution of di-n-butylamine / toluene (weight ratio: 2/25) with 90 mL of acetone, titrating with 0.5 N hydrochloric acid aqueous solution, measuring the amount of hydrochloric acid aqueous solution required for neutralization, and blank value It was. Thereafter, 1 to 2 g of the reaction solution was extracted, 20 mL of a mixed solution of di-n-butylamine / toluene was added, and the mixture was stirred at room temperature for 30 minutes. The amount of hydrochloric acid aqueous solution required for neutralization was measured by titration with, and the amount of remaining amine was quantified. The concentration of the isocyanate group was determined from the volume of the aqueous hydrochloric acid solution required for neutralization by the following formula.
Isocyanate group concentration (% by weight) = A * 42.02 / D
A: Isocyanate group (mol) contained in the sample used in this measurement
A = (B−C) × 0.5 / 1000 × f
B: Amount of 0.5N hydrochloric acid aqueous solution required for blank measurement (mL)
C: Amount of 0.5N hydrochloric acid aqueous solution required for this measurement (mL)
D: Sample used for this measurement (g)
f: Potency of aqueous hydrochloric acid solution

<Measurement of solution viscosity>
A solution of polyurethane dissolved in dimethylformamide (concentration: 30% by weight) was set on a VISCOMETER TV-22 (manufactured by Toki Sangyo Co., Ltd.) with a 3 ° × R14 rotor, and the solution viscosity of the polyurethane solution was measured at 25 ° C. .

<Molecular weight measurement>
Prepare a dimethylacetamide solution so that the polyurethane has a molecular weight of 0.14% by weight and a GPC apparatus (product name “HLC-8220” manufactured by Tosoh Corporation (column: Tskel GMH-XL × 2)) The number average molecular weight (Mn) and weight average molecular weight (Mw) in terms of standard polystyrene were measured.

<Oleic acid resistance evaluation method>
The polyurethane solution was applied on a fluororesin sheet (fluorine tape Nittofuron 900, thickness 0.1 mm, manufactured by Nitto Denko Corporation) with a 9.5 mil applicator, and then 0.5 hours at 100 ° C. for 1 hour at 60 ° C. Let dry for hours. Furthermore, in a vacuum state of 100 ° C., 0.5 hours, 8
After drying at 0 ° C. for 15 hours, the sample was allowed to stand for 12 hours or more at a constant temperature and humidity of 23 ° C. and 55% RH, and a 3 cm × 3 cm test piece was cut out from the resulting film, and a volume of 250 ml containing 50 ml of the test solvent. Were placed in a glass bottle and allowed to stand for 1 week or 16 hours in a thermostatic bath in a nitrogen atmosphere at 80 ° C. After the test, after lightly wiping the front and back of the test piece with a paper wiper, the weight was measured and the weight increase ratio from before the test was calculated. A weight change rate closer to 0% indicates better oleic acid resistance.

<Polyurethane ethanol resistance evaluation method>
A urethane film was prepared in the same manner as described in the above <Method for evaluating resistance to oleic acid>, and then a urethane film test piece cut out to 3 cm × 3 cm was cut out. After measuring the weight of the test piece with a precision balance, it was put into a glass petri dish having an inner diameter of 10 cmφ containing 50 ml of a test solvent and immersed at room temperature of about 23 ° C. for 1 hour. After the test, the test piece was taken out and lightly wiped with a paper wiper, and then the weight was measured to calculate the weight increase ratio from before the test.

<Method of measuring glass transition temperature (Tg)>
About 5 mg of a polyurethane film piece prepared in the same manner as in the evaluation of oleic acid resistance was enclosed in an aluminum pan, and EXSTAR DSC6200 (manufactured by Seiko Instruments Inc.) was used. From 250 ° C. to 250 ° C., from −100 ° C. to −100 ° C., and from −100 ° C. to 250 ° C.

<Room temperature tensile test method>
According to JIS K6301 (2010), using a tensile tester [product name “Tensilon UTM-III-100” manufactured by Orientec Co., Ltd.] Then, a tensile test was performed at a temperature of 23 ° C. (relative humidity 55%) at a distance between chucks of 50 mm and a tensile speed of 500 mm / min. The Young's modulus is the slope of the stress value at the initial elongation, specifically, the stress value when the elongation is 1%.

<Low temperature tensile test method>
In accordance with JIS K6301 (2010), a polyurethane test piece having a strip shape having a width of 10 mm, a length of 100 mm, and a thickness of about 50 μm was used as a tensile tester [manufactured by Shimadzu Corporation, product name “Autograph AG-X 5kN”. ], A film was placed in a thermostatic bath set to −10 ° C. [manufactured by Shimadzu Corporation, product name “THERMOSTATIC CHAMBER TCR2W-200T”] with a chuck distance of 50 mm. Then, after leaving still at -10 degreeC for 3 minute (s), the tension test was implemented at the tension speed of 500 mm / min, and the stress at the time of test piece extending | stretching 100% was measured. The Young's modulus is the slope of the stress value at the initial elongation, specifically, the stress value when the elongation is 1%.

<Polyurethane low temperature cycle test method>
In accordance with JIS K6301 (2010), a polyurethane test piece having a strip shape having a width of 10 mm, a length of 100 mm, and a thickness of about 90 μm was used as a tensile tester [manufactured by Shimadzu Corporation, product name “Autograph AG-X 5kN”. , Using a load cell 100N], a film was placed in a thermostatic bath set to −10 ° C. [manufactured by Shimadzu Corporation, product name “THERMOSTATIC CHAMBER TCR2W-200T”] with a distance between chucks of 50 mm. Then, after leaving still at -10 degreeC for 3 minute (s), it extended | stretched to 300% at the tensile speed of 500 mm / min, and it was made to shrink | contract to the original length at the same speed, and this was repeated twice. The ratio of the stress at the time of 250% elongation at the first contraction (hereinafter sometimes referred to as “ratio 1”) to the stress at the time of 250% elongation at the first elongation was determined. In addition, the stress at the time of 250% elongation at the time of the second elongation (hereinafter also referred to as “ratio 2”) was obtained with respect to the stress at the time of 250% elongation at the first elongation.

<Heat resistance evaluation>
The polyurethane film prepared in the same manner as in the oleic acid resistance evaluation is formed into a strip shape having a width of 100 mm, a length of 100 mm, and a thickness of about 50 μm, and heated in a gear oven at a temperature of 120 ° C. for 400 hours. (Mw) was measured by the method described in <Molecular weight measurement>.

<Raw materials>
The raw materials used for the production of the polycarbonate diol of this example are as follows.
1,4-butanediol (hereinafter sometimes abbreviated as 1,4BD): manufactured by Mitsubishi Chemical Corporation 1,5-pentadiol (hereinafter sometimes abbreviated as 1,5PD): manufactured by Tokyo Chemical Industry Co., Ltd. 1,3-propanediol (hereinafter sometimes abbreviated as 1,3PDO): 1,6-hexanediol (hereinafter, abbreviated as 1,6HD) manufactured by Wako Pure Chemical Industries, Ltd. or DuPont Co., Ltd. ): BASF 1,10-decanediol (hereinafter sometimes abbreviated as 1,10DD): Toyokuni Oil Co., Ltd. 1,9-nonanediol (hereinafter sometimes abbreviated as 1,9ND): Tokyo 1,12-dodecanediol (hereinafter, may be abbreviated as 1,12 DDD) manufactured by Kasei Kogyo Co., Ltd .: 2-methyl-1,3-propanediol (hereinafter referred to as Wako Pure Chemical Industries, Ltd.) Below, it may be abbreviated as 2M1,3PDO): Tokyo Chemical Industry Co., Ltd. 3-methyl-1,5-pentanediol (hereinafter abbreviated as 3M1,5PD): Wako Pure Chemical Industries, Ltd. Diphenyl carbonate (hereinafter sometimes abbreviated as DPC): Mitsubishi Chemical Corporation ethylene carbonate (hereinafter sometimes abbreviated as EC): Mitsubishi Chemical Corporation magnesium acetate tetrahydrate: Wako Pure Chemical Industries, Ltd. Company-made lead acetate (II) trihydrate: Wako Pure Chemical Industries, Ltd. Lead acetate (IV): Nacalai Tesque

[Example 1]
<Manufacture and evaluation of polycarbonate diol>
In a 5 L glass separable flask equipped with a stirrer, a distillate trap, and a pressure regulator, 1,4-butanediol (1,4BD): 768.5 g, 1,10-decanediol (1,1) 10DD): 768.5 g, diphenyl carbonate: 2563.0 g, magnesium acetate tetrahydrate aqueous solution: 6.6 mL (concentration: 8.4 g / L, magnesium acetate tetrahydrate: 55 mg), and purged with nitrogen gas . Under stirring, the internal temperature was raised to 160 ° C., and the contents were dissolved by heating. Thereafter, the pressure was lowered to 24 kPa over 2 minutes, and then reacted for 90 minutes while removing phenol out of the system. Next, the pressure is lowered to 9.3 kPa over 90 minutes and further lowered to 0.7 kPa over 30 minutes, and then the reaction is continued, and then the temperature is raised to 170 ° C. to remove phenol and unreacted dihydroxy compounds out of the system. For 60 minutes to obtain a polycarbonate diol-containing composition.

The obtained polycarbonate diol-containing composition was fed to a thin film distillation apparatus at a flow rate of 20 g / min, and thin film distillation (temperature: 180 to 190 ° C., pressure: 40 to 67 Pa) was performed. As the thin-film distillation apparatus, an internal condenser having a diameter of 50 mm, a height of 200 mm, and an area of 0.0314 m2, a special model of molecular distillation apparatus MS-300 manufactured by Shibata Kagaku Co., Ltd. with a jacket was used.
The same applies to the following examples and comparative examples.
Table 1 shows the evaluation results of properties and physical properties of the polycarbonate diol obtained by thin film distillation.

<Manufacture and evaluation of polyurethane>
Using the polycarbonate diol obtained by the above method, a specific polyurethane was produced by the following operation.
(Prepolymer (PP) reaction)
In a separable flask equipped with a thermocouple and a condenser tube, 90.57 g of the above polycarbonate diol heated to 80 ° C. was put in advance, and the flask was immersed in an oil bath at 60 ° C., and then 4,4′-dicyclohexylmethane. Diisocyanate (hereinafter, H12MDI, manufactured by Tokyo Chemical Industry Co., Ltd.) (22.69 g) and triisooctyl phosphite (hereinafter, TiOP, manufactured by Tokyo Chemical Industry Co., Ltd.) (0.332 g) as a reaction inhibitor are added, and the flask is filled with a nitrogen atmosphere. The temperature was raised to 80 ° C. in about 1 hour while stirring at 60 rpm. After raising the temperature to 80 ° C., 9.3 mg of Neostan U-830 (hereinafter referred to as U-830, manufactured by Nitto Kasei Co., Ltd.) as a urethanization catalyst was added (81.9 wtppm with respect to the total weight of polycarbonate dio and isocyanate) to generate heat. Then, the oil bath was heated to 100 ° C. and further stirred for about 2 hours. The concentration of the isocyanate group was analyzed, and it was confirmed that the theoretical amount of the isocyanate group was consumed.

(Chain extension reaction)
106.62 g of the obtained prepolymer (PP) was diluted with 11.46 g of dehydrated toluene (manufactured by Wako Pure Chemical Industries, Ltd.). Subsequently, 237.36 g of dehydrated N, N-dimethylformamide (hereinafter DMF, manufactured by Wako Pure Chemical Industries, Ltd.) was added, the flask was immersed in an oil bath at 55 ° C., and the prepolymer was dissolved while stirring at about 200 rpm. After analyzing the concentration of isocyanate groups in the prepolymer solution, the flask was immersed in an oil bath set at 35 ° C., and the required amount of isophorone diamine calculated from the remaining isocyanate (hereinafter referred to as IPDA, manufactured by Tokyo Kasei) 6 while stirring at 150 rpm. 0.06 g was added in portions. After stirring for about 1 hour, 0.623 g of morpholine (manufactured by Tokyo Chemical Industry Co., Ltd.) is added as a terminal terminator, and the mixture is further stirred for 1 hour to obtain a polyurethane solution having a viscosity of 125 Pa · s and a weight average molecular weight of 151,000. It was. Table 3 shows the evaluation results of the properties and physical properties of this polyurethane.

[Examples 2 to 13]
<Manufacture and evaluation of polycarbonate diol>
In the production of the polycarbonate diol of Example 1, all the reactions were carried out under the same conditions and methods except that the types and amounts of PCD polymerization raw materials were changed to the types and amounts of raw materials shown in Table 1. A containing composition was obtained.
The obtained polycarbonate diol-containing composition was subjected to thin film distillation in the same manner as in Example 1. Table 1 shows the evaluation results of properties and physical properties of the polycarbonate diol obtained by thin film distillation.

<Manufacture and evaluation of polyurethane>
In the production of the polyurethane of Example 1, the reaction was carried out under the same conditions and methods, except that the type of polycarbonate diol (PCD) used and the charged amount of each raw material were changed to the PCD and charged amount shown in Table 3, respectively. To obtain a polyurethane solution. Table 3 shows the properties and physical properties of this polyurethane.

[Comparative Example 1 and Comparative Example 5]
<Manufacture and evaluation of polycarbonate diol>
In the production of the polycarbonate diol of Example 1, the reaction was carried out under the same conditions and methods except that the types and amounts of the PCD polymerization raw materials were changed to the raw materials and the amounts of raw materials shown in Table 2. A containing composition was obtained.

The obtained polycarbonate diol-containing composition was subjected to thin film distillation in the same manner as in Example 1.
Table 2 shows the evaluation results of properties and physical properties of polycarbonate diol obtained by thin film distillation.

<Manufacture and evaluation of polyurethane>
In the production of the polyurethane of Example 1, the reaction was carried out under the same conditions and methods except that the polycarbonate diol (PCD) to be used and the charge amount of each raw material were changed to the charge amounts shown in Table 3, respectively. A solution was obtained. Table 3 shows the evaluation results of the properties and physical properties of this polyurethane.

[Comparative Examples 2 to 4, Comparative Example 6]
<Evaluation of polycarbonate diol>
The following polycarbonate diols were used. Table 2 shows the evaluation results of properties and physical properties of each polycarbonate diol.
Comparative Example 2: Polycarbonate diol produced using 1,6HD as a raw material ("Duranol (registered trademark)" grade: T-6002 manufactured by Asahi Kasei Chemicals Corporation)
Comparative Example 3: Polycarbonate diol produced from 1,4BD and 1,6HD as raw materials ("Duranol (registered trademark)" grade: T-4672, manufactured by Asahi Kasei Chemicals Corporation)
Comparative Example 4: Polycarbonate diol produced using 1,5PD and 1,6HD as raw materials ("Duranol (registered trademark)" grade: T-5552 manufactured by Asahi Kasei Chemicals Corporation)
Comparative Example 6: Polycarbonate diol using 1,9ND, 2M1,8OD as raw materials (trade name: Kuraray polyol C-2065N manufactured by Kuraray Co., Ltd.)
<Manufacture and evaluation of polyurethane>
Polyurethane was produced using the above polycarbonate diol as PCD as a polyurethane production raw material.

  In the production of the polyurethane of Example 1, the reaction was carried out under the same conditions and methods except that the polycarbonate diol used as the raw material and the raw material charge amount were changed to the raw material types and respective charge amounts shown in Table 3. To obtain a polyurethane solution. Table 3 shows the evaluation results of the properties and physical properties of this polyurethane.

[Comparative Example 7]
<Manufacture and evaluation of polycarbonate diol>
In the production of the polycarbonate diol of Example 1, the raw materials and the charged amounts of the raw materials were all changed in the same manner except that the raw materials (1,6HD and 3M1,5PD) and the charged amounts of the raw materials shown in Table 2 were changed. Reaction was performed and the polycarbonate containing composition was obtained.

The obtained polycarbonate diol-containing composition was subjected to thin film distillation in the same manner as in Example 1.
Table 2 shows the evaluation results of properties and physical properties of polycarbonate diol obtained by thin film distillation.

<Manufacture and evaluation of polyurethane>
The polycarbonate diol obtained by the above method and the polycarbonate diol used in Comparative Example 6 (trade name: Kuraray Polyol C-2065N, manufactured by Kuraray Co., Ltd.) are mixed at a weight ratio of 75:25 for the production of polyurethane. A raw material (PCD) was used.

In the production of the polyurethane of Example 1, the raw material (PCD) obtained by this mixing was used, and the reaction was carried out under the same conditions and methods except that the raw material charge amount was changed to the charge amount shown in Table 3. And a polyurethane solution was obtained. Table 3 shows the evaluation results of the properties and physical properties of this polyurethane.
In “Stress at −10 ° C./100% elongation” in Table 3, the value of the example is smaller than that of the comparative example, indicating that the flexibility at low temperature is good. Further, since the values of “80 ° C. resistance to oleic acid weight change” and “room temperature resistance to ethanol weight change” are small, it is understood that the chemical resistance is good. Furthermore, since the value of “change rate of polystyrene-equivalent weight average molecular weight after the heat test” is small, it can be seen that the heat resistance is good, and the examples show that the physical properties are good. Therefore, it can be seen that the polycarbonate diol of the present invention is a polycarbonate diol as a raw material for polyurethane, which is excellent in the balance of chemical resistance, low temperature characteristics and heat resistant physical properties as compared with the conventional polycarbonate diol.

The meanings of the abbreviations in Tables 1 and 2 are as follows.
1,4BD ... 1,4-butanediol 1,5PD ... 1,5-pentadiol 1,3PDO ... 1,3-propanediol 1,6HD ... 1,6-hexanediol 1,10DD ... 1,10-decanediol 1,9ND ... 1,9-nonanediol 1,12DDD ... 1,12-dodecanediol 2M1,3PDO ... 2-methyl-1,3-propanediol 2M1,8OD ... 2-methyl-1,8-octanediol 3M1, 5PD ... 3-methyl-1,5-pentanediol DPC ... diphenyl carbonate

Claims (15)

A polycarbonate diol comprising a structural unit derived from a compound represented by the following formula (A) and a structural unit derived from a compound represented by the following formula (B),
The compound represented by the formula (A) is 1,3-propanediol and 1,4-butanedio
At least one compound selected from the group consisting of
The compound represented by the formula (B) is 1,9-nonanediol, 1,10-decandioe.
1,11-undecanediol, 1,12-dodecanediol, 1,13-trideca
Diol, 1,14-tetradecanediol, 1,16-hexadecanediol, 1,
Selected from the group consisting of 18-octadecanediol and 1,20-eicosanediol
At least one compound,
The hydroxyl value is 20 mg-KOH / g or more and 450 mg-KOH / g or less,
The ratio of the structural unit derived from the compound represented by the following formula (A) and the structural unit derived from the compound represented by the following formula (B) is 70:30 to 99: 1 in molar ratio. Polycarbonate diol.
HO—R ¹ —OH (A)
HO—R ² —OH (B)
(In the formula (A), R ¹ represents a substituted or unsubstituted divalent alkylene group having 3 to 5 carbon atoms, and in the formula (B), R ² represents an unsubstituted 9 to carbon atoms. This represents a divalent alkylene group of formula 20. The total proportion of the structural unit derived from the compound represented by the formula (A) and the structural unit derived from the compound represented by the formula (B) is 50 in all the structural units of the polycarbonate diol.
The polycarbonate diol according to claim 1, wherein the polycarbonate diol is at least mol%. The polycarbonate diol according to claim 1 or 2 , wherein an average number of carbon atoms of a dihydroxy compound obtained by hydrolyzing the polycarbonate diol is 4 or more and 5.5 or less. The hydroxyl value is 20 mg-KOH / g or more and 60 mg-KOH / g or less.
4. The polycarbonate diol according to any one of 3 . 2. The compound represented by the formula (B) is at least one compound selected from the group consisting of 1,9-nonanediol, 1,10-decanediol, and 1,12-dodecanediol. The polycarbonate diol according to any one of to 4 . The polycarbonate diol according to any one of claims 1 to 5 , wherein at least one of the compound represented by the formula (A) and the compound represented by the formula (B) is derived from a plant. An ester group is introduced by reaction with at least one compound selected from the group consisting of cyclic lactones, dicarboxylic acid compounds and ester compounds of dicarboxylic acid compounds.
The polycarbonate diol according to any one of to 6 . A polyurethane comprising the polycarbonate diol according to any one of claims 1 to 7 . Artificial leather or synthetic leather produced using the polyurethane according to claim 8 . A paint or coating agent produced using the polyurethane according to claim 8 . The elastic fiber manufactured using the polyurethane of Claim 8 . A water-based polyurethane paint produced using the polyurethane according to claim 8 . A pressure-sensitive adhesive or adhesive produced using the polyurethane according to claim 8 . An active energy ray-curable polymer composition comprising the polycarbonate diol according to any one of claims 1 to 7 . A method for producing the polycarbonate diol according to any one of claims 1 to 7 ,
At least selected from the group consisting of 1,3-propanediol and 1,4-butanediol
Both one compound (A),
1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol
1,12-dodecanediol, 1,13-tridecanediol, 1,14-tetradecane
Diol, 1,16-hexadecanediol, 1,18-octadecanediol, and
At least one compound (B) selected from the group consisting of 1,20-eicosanediol;
,
A process for producing a polycarbonate diol, characterized in that polycondensation is carried out by transesterification using a carbonate compound .