JP2012001620A - Polylactic acid composition, and molded article formed therefrom - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a polylactic acid composition which has superior molding processability, exhibits improved hydrolysis resistance, produces no free isocyanate in a strp, and is suitable for industrial production.SOLUTION: The polylactic acid composition is mainly composed of a polylactic acid component (A), wherein, with regard to the resin composition, the polylactic acid composition contains 95-99.99 wt.% of the polylactic acid component (A), 0.01-5 wt.% of an α-hydroxycarboxylic acid component (B) other than lactic acid, and 0.01-10 wt.% of a carbodiimide compound (C) of a particular structure per 100 wt.% of component (A) and component (B) combined.

Description

  The present invention relates to a polylactic acid composition, and more specifically, it is composed of a polylactic acid component and an α-hydroxycarboxylic acid component other than lactic acid, and has good heat resistance and molding processability and is suitable for industrial production. The present invention relates to a polylactic acid composition and fibers, films, and resin molded articles comprising the same.

  In recent years, for the purpose of protecting the global environment, biodegradable polymers that are decomposed in a natural environment have attracted attention and are being studied all over the world. As biodegradable polymers, aliphatic polyesters such as polylactic acid, polyhydroxybutyrate and polycaprolactone are known. Since polylactic acid uses lactic acid obtained from a raw material derived from a living body or a derivative thereof as a raw material, it is a high-safety and environmentally friendly polymer material. Therefore, the use as a general-purpose polymer is examined, and the use as a stretched film, a fiber, an injection molded product, etc. is examined.

  However, polylactic acid has a low glass transition point of 58 ° C. and a crystal melting temperature of about 155 ° C., so there is a limit to heat resistance, and since it is easily decomposed by humidity, it has a limit to moist heat resistance and further has a crystallization rate. Since it is slow, there is a limit to the formability of crystallized and used as a molded product.

  In order to improve moldability, a method of adding a crystallization accelerating agent such as a crystallization nucleating agent (for example, Patent Document 1), and a method in which a phosphoric acid ester metal salt of a crystallization nucleating agent and a fatty acid amide are used in combination. (For example, patent document 2 etc.), the method (for example, patent document 3 etc.) of adding an organic and inorganic filler is proposed conventionally.

  With these proposals, some improvement has been seen in improving the crystallization speed and heat resistance of polylactic acid, that is, homopolymers consisting of L-lactic acid units and D-lactic acid units, random copolymers, block copolymers, and mixtures thereof. However, no mention is made of a polylactic acid composition containing a stereocomplex phase.

  That is, poly L-lactic acid (hereinafter sometimes abbreviated as PLLA) composed of L-lactic acid units and poly D-lactic acid (hereinafter sometimes abbreviated as PDLA) composed of D-lactic acid units in a solution or in a molten state. It is known that stereocomplex polylactic acid is formed by mixing (Patent Document 4).

This stereocomplex polylactic acid has a crystal melting temperature of 200 to 230 ° C., a higher melting point than PLLA and PDLA, and an interesting phenomenon showing high crystallinity has been discovered.
However, formation of stereocomplex polylactic acid is not easy, and the difficulty becomes even more pronounced especially when the weight average molecular weight of PLLA or PDLA exceeds 150,000 (Patent Document 4).

That is, the stereocomplex polylactic acid usually does not show a single phase, but a PLLA phase and a PDLA phase (hereinafter sometimes referred to as a homophase) and a polylactic acid stereocomplex phase (hereinafter sometimes referred to as a complex phase). This is a mixed phase composition.
In this mixed phase composition, if the proportion of the complex phase is small, it is difficult to exhibit the heat resistance inherent in stereocomplex polylactic acid.

  In addition, it has already been proposed to add a carbodiimide compound to polylactic acid and use it as a carboxyl group-terminal sealing agent to suppress hydrolysis of polylactic acid (for example, Patent Document 5). The carbodiimide compound used in this proposal is a linear carbodiimide compound.

  When a linear carbodiimide compound is used as a polymer end-capping agent, a compound having an isocyanate group is liberated along with a reaction in which the linear carbodiimide compound is bonded to the end of the polymer, and a unique odor of the isocyanate compound is generated. It has become a problem to deteriorate.

JP 2003-192894 A JP 2004-224990 A Japanese Patent Laid-Open No. 2005-2174 JP 63-24014 A JP 2006-63111 A

An object of the present invention is to provide a polylactic acid composition suitable for industrial production, which has excellent molding processability, improves hydrolysis resistance, and does not generate free isocyanate during the process. is there.
It is another object of the present invention to provide a polylactic acid composition containing stereocomplex polylactic acid and having the above properties and excellent heat resistance.

The present inventor completed the present invention as a result of intensive studies to solve the above problems.
That is, the object of the present invention is to
1. A polylactic acid composition comprising a polylactic acid (A) component as a main component, wherein the polylactic acid (A) component is 95 wt% or more and 99.99 wt% or less based on the resin composition, and α- other than lactic acid The hydroxycarboxylic acid (B) component is 0.01% by weight or more and 5% by weight or less, and the carbodiimide compound (C) represented by the following structural formula is added per 100% by weight of the total amount of the components (A) and (B). Achieved by a polylactic acid composition comprising 0.01 to 10% by weight.

（式中、Ｑは、二価の有機基を示す、）

(In the formula, Q represents a divalent organic group.)

  According to the present invention, it is possible to provide a polylactic acid composition suitable for industrial production that has excellent molding processability, improves hydrolysis resistance, and does not generate free isocyanate during the process. it can.

Hereinafter, the present invention will be described in detail.
The polylactic acid composition of the present invention is a polylactic acid composition mainly comprising a polylactic acid (A) component, and the polylactic acid (A) component is 95 wt% or more and 99.99 based on the resin composition. Less than wt%, α-hydroxycarboxylic acid (B) component other than lactic acid is 0.01 wt% or more and 5 wt% or less, carbodiimide compound (C) represented by the following structural formula, (A) component and (B) This is achieved by including 0.01 to 10% by weight per 100% by weight of the total amount of components.

（式中、Ｑは、二価の有機基を示す、）

(In the formula, Q represents a divalent organic group.)

  By setting the polylactic acid composition of the present invention to such a composition, the polylactic acid composition of the present invention is favorable with heat resistance and molding processability, which are the objects of the present invention, and can be suitably produced industrially.

Hereinafter, each component in the polylactic acid composition of the present invention will be described.
<Polylactic acid (A) component>
The polylactic acid (A) component of the present invention may be a poly L-lactic acid component or a poly D-lactic acid component.
Each of poly L-lactic acid and poly D-lactic acid has a crystal melting peak (Tmh) and a glass transition point (Tg) of 60 ° C. or higher between 150 ° C. and 190 ° C. as measured by differential scanning calorimetry (DSC). The crystal melting heat (ΔHmsc) is preferably 10 J / g or more.
This is because the heat resistance of the polylactic acid (A) can be suitably increased by satisfying the range of the crystal melting point and the crystal melting heat.

Furthermore, in this invention, the stereocomplex polylactic acid which consists of poly L lactic acid and poly D lactic acid is also included from a heat resistant viewpoint. The polylactic acid used here is a poly-L-lactic acid copolymer having a poly-L-lactic acid component of 95% by weight or more and an α-hydroxycarboxylic acid component other than lactic acid described later of 5% by weight or less, and a poly-D-lactic acid. A stereocomplex polylactic acid is prepared by mixing 95% by weight or more of the component with a poly D-lactic acid copolymer containing 5% by weight or less of an α-hydroxycarboxylic acid component other than lactic acid, which will be described later. The stereocomplex crystallinity defined in i) is preferably selected in the range of 90% to 100%, more preferably 95% to 100%. Particularly preferred is when the stereocomplex crystallinity is 100%.
S = [ΔHms / (ΔHmh + ΔHms)] × 100 (i)
(However, ΔHms = Crystal melting enthalpy of stereocomplex phase polylactic acid and ΔHmh = Polylactic acid homophase crystal melting enthalpy)

Further, the stereocomplex polylactic acid preferably has crystallinity, and the stereocomplex crystallization rate (Sc) defined by the following formula (ii) is determined by the intensity ratio of diffraction peaks by wide-angle X-ray diffraction (XRD) measurement. ) Is more preferably 50% or more.
Sc (%) = [ΣI _SCi / (ΣI _SCi + I _HM )] × 100 (ii)
[Where ΣI _SCi = I _SC1 + I _SC2 + I _SC3 and I _SCi (i = 1 to 3) are integrals of diffraction peaks around 2θ = 12.0 °, 20.7 °, and 24.0 °, respectively. _{intensity, I HM} represents the integrated intensity _{I HM} of a diffraction peak derived from homo-phase crystal appearing near 2θ = 16.5 °. ]

  Further, from the same viewpoint, the crystal melting point of the stereocomplex phase polylactic acid is suitably selected in the range of 190 to 250 ° C., more preferably 200 to 230 ° C., and the crystal melting enthalpy by DSC measurement is 20 J / g or more, preferably A range of 20 to 80 J / g, more preferably 30 to 80 J / g is selected.

  If the crystal melting point of the stereocomplex phase polylactic acid is less than 190 ° C., the significance of the formation of the stereocomplex phase, and thus the significance of the present invention, will be small. Furthermore, when exceeding 250 degreeC, when shape | molding the molded article of this invention, it will be necessary to shape | mold at the high temperature of 250 degreeC or more, and it may become difficult to suppress the thermal decomposition of a polylactic acid composition. The same argument applies to the value of crystal melting enthalpy.

  In order to suitably satisfy the stereocomplex crystallinity, stereocomplex crystallinity, and various crystallinity parameters described above, in the polylactic acid (A) component, the weight ratio of the poly L-lactic acid component to the poly D-lactic acid component Is preferably 90/10 to 10/90.

  More preferably, it is in the range of 80/20 to 20/80, more preferably 30/70 to 70/30, particularly preferably 40/60 to 60/40, and theoretically preferably as close to 1/1 as possible. Selected.

  In the present invention, the poly-D-lactic acid component is represented by the following formula (iv), and is composed of D-lactic acid units, preferably 90 to 100 mol% D-lactic acid units and 0 to 10 mol% D-. Consists of copolymer units other than lactic acid units. A range of 95 to 100 mol% is more preferable, and a range of 98 to 100 mol% is more preferable.

  The poly L-lactic acid component is represented by the following formula (iv), and is composed of L-lactic acid units, preferably 90 to 100 mol% L-lactic acid units and 0 to 10 mol% L-lactic acid units. It consists of copolymerized units other than. A range of 95 to 100 mol% is more preferable, and a range of 98 to 100 mol% is more preferable.

  In the poly L-lactic acid component and the poly D-lactic acid component, the copolymer unit is composed of units derived from dicarboxylic acid, polyhydric alcohol, lactone and the like having a functional group capable of forming two or more ester bonds and these various constituent components. Units derived from various polyesters, various polyethers, various polycarbonates and the like are exemplified.

  Examples of the dicarboxylic acid include succinic acid, adipic acid, azelaic acid, sebacic acid, terephthalic acid, and isophthalic acid. Examples of the polyhydric alcohol include aliphatic polyhydric alcohols such as ethylene glycol, propylene glycol, butanediol, pentanediol, hexanediol, octanediol, glycerin, sorbitan, neopentyl glycol, diethylene glycol, triethylene glycol, polyethylene glycol, and polypropylene glycol. Or aromatic polyhydric alcohol etc., such as what added ethylene oxide to bisphenol, etc. are mentioned. Examples of the lactone include glycolide, ε-caprolactone, β-propiolactone, δ-butyrolactone, β- or γ-butyrolactone, pivalolactone, and δ-valerolactone.

  The weight average molecular weights of the poly L-lactic acid and poly D-lactic acid components of the present invention are preferably 100,000 to 500,000, more preferably 110,000 to 35, in order to achieve both the mechanical properties and moldability of the molded article of the present invention. A range of 10,000, more preferably 12 to 250,000 is selected.

Poly L-lactic acid and poly D-lactic acid can be produced by a conventionally known method.
For example, it can be produced by ring-opening polymerization of L-lactide or D-lactide in the presence of a metal-containing catalyst. In addition, low molecular weight polylactic acid containing a metal-containing catalyst is crystallized as desired or without crystallization, under reduced pressure or from normal pressure, in the presence of an inert gas stream, or absent It can also be produced by solid phase polymerization. Furthermore, it can be produced by a direct polymerization method in which lactic acid is subjected to dehydration condensation in the presence or absence of an organic solvent.

  The polymerization reaction can be carried out in a conventionally known reaction vessel. For example, in a ring-opening polymerization or direct polymerization method, a vertical reactor or a horizontal reactor equipped with a stirring blade for high viscosity, such as a helical ribbon blade, is used alone, or Can be used in parallel. Moreover, any of a batch type, a continuous type, a semibatch type may be sufficient, and these may be combined.

  Alcohol may be used as a polymerization initiator. Such alcohol is preferably non-volatile without inhibiting the polymerization of polylactic acid, such as decanol, dodecanol, tetradecanol, hexadecanol, octadecanol, ethylene glycol, trimethylolpropane, pentaerythritol, etc. Can be suitably used.

  It can be said that the polylactic acid prepolymer used in the solid-phase polymerization method is preferably crystallized in advance from the viewpoint of preventing pellet fusion. The prepolymer is polymerized in a solid state in a fixed vertical or horizontal reaction vessel, or in a reaction vessel (such as a rotary kiln) that rotates itself like a tumbler or kiln, in the temperature range from the glass transition temperature of the prepolymer to less than the melting point. Is done.

  Metal-containing catalysts include alkali metals, alkaline earth metals, rare earths, transition metals, fatty acid salts such as aluminum, germanium, tin, antimony, titanium, carbonates, sulfates, phosphates, oxides, hydroxides , Halides, alcoholates and the like.

  Among them, fatty acid salts, carbonates, sulfates, phosphates, oxides, hydroxides containing at least one metal selected from tin, aluminum, zinc, calcium, titanium, germanium, manganese, magnesium and rare earth elements Products, halides, and alcoholates are preferred.

  Tin compounds due to low catalytic activity and side reactions, specifically stannous chloride, stannous bromide, stannous iodide, stannous sulfate, stannic oxide, tin myristate, tin octylate Tin-containing compounds such as tin stearate and tetraphenyltin are exemplified as preferred catalysts.

  Among these, tin (II) compounds, specifically, diethoxytin, dinonyloxytin, tin (II) myristate, tin (II) octylate, tin (II) stearate, tin (II) chloride and the like are suitable. Illustrated.

The amount of the catalyst used is 0.42 × 10 ⁻⁴ to 100 × 10 ⁻⁴ (mol) per 1 kg of lactide, and is 1.68 × 10 ^{−4 in} consideration of reactivity, color tone and stability of the resulting polylactides. To 42.1 × 10 ⁻⁴ (mol), particularly preferably 2.53 × 10 ⁻⁴ to 16.8 × 10 ⁻⁴ (mol) mol.

The metal-containing catalyst used for polylactic acid polymerization is preferably deactivated with a conventionally known deactivator prior to using polylactic acid.
Examples of such a deactivator include an organic ligand comprising a group of chelate ligands having an imino group and capable of coordinating to a polymerized metal catalyst, dihydridooxoline (I) acid, dihydridotetraoxodilin (II, II ) Acid, hydridotrioxoline (III) acid, dihydridopentaoxodiphosphorus (III) acid, hydridopentaoxodi (II, IV) acid, dodecaoxohexaphosphorus (III) acid, hydridooctaoxotriphosphate (III, IV) , IV) acid, octaoxotriphosphoric acid (IV, III, IV), hydridohexaoxodiphosphoric acid (III, V), hexaoxodiphosphoric acid (IV), decaoxotetralinic acid (IV), hedecaoxotetralinic acid (IV ) acid, Eneaokiso triphosphate (V, IV, IV) acid value 5 or less low oxidation number phosphoric acids such as acids, _{wherein, xH 2 O · yP 2 O} 5 X-y = 3 orthophosphoric acid, 2> x / y> 1, polyphosphoric acid referred to as diphosphoric acid, triphosphoric acid, tetraphosphoric acid, pentaphosphoric acid and the like based on the degree of condensation, and mixtures thereof , X / y = 1, especially trimetaphosphoric acid, tetrametaphosphoric acid, 1> x / y> 0, ultralin having a network structure with a part of the phosphorus pentoxide structure Acids (sometimes collectively referred to as metaphosphoric acid compounds), and acid salts of these acids, monovalent and polyhydric alcohols, or partial esters of polyalkylene glycols, fully ether, phosphono substitution Examples include lower aliphatic carboxylic acid derivatives.

From the viewpoint of catalyst deactivation ability, it is represented by the formula xH ₂ O · yP ₂ O ₅ , x / y = 3 orthophosphoric acid, 2> x / y> 1, and the degree of condensation is diphosphoric acid, triphosphorus Polyphosphoric acid referred to as acid, tetraphosphoric acid, pentaphosphoric acid and the like, and mixtures thereof, metaphosphoric acid represented by x / y = 1, especially trimetaphosphoric acid, tetrametaphosphoric acid, 1> x / y> 0 And an ultraphosphoric acid having a network structure in which part of the phosphorus pentoxide structure is left (sometimes collectively referred to as a metaphosphoric acid compound), and acid salts of these acids, monovalent, polyvalent Alcohols of the above, partial esters of polyalkylene glycols, phosphorus oxoacids or acidic esters thereof, phosphono-substituted lower aliphatic carboxylic acid derivatives and the above-mentioned metaphosphoric acid compounds are preferably used.

  The metaphosphoric acid compound used in the present invention is a cyclic metaphosphoric acid in which about 3 to 200 phosphoric acid units are condensed, an ultra-regional metaphosphoric acid having a three-dimensional network structure, or their (alkal metal salt, alkaline earth metal salt, Onium salts).

  Among them, cyclic sodium metaphosphate, ultra-region sodium metaphosphate, phosphono-substituted lower aliphatic carboxylic acid derivative dihexylphosphonoethyl acetate (hereinafter sometimes abbreviated as DHPA) and the like are preferably used.

<Α-hydroxycarboxylic acid (B) component other than lactic acid>
In the α-hydroxycarboxylic acid (B) component other than lactic acid of the present invention, R ′ is composed of hydrogen or an aliphatic alkyl group, as shown by the following formula.

（式中Ｒ’は水素原子、または脂肪族アルキル基を表す。）

(In the formula, R ′ represents a hydrogen atom or an aliphatic alkyl group.)

  In order to achieve the object of the present invention, it is essential that the α-hydroxycarboxylic acid (B) component other than lactic acid is contained in an amount of 0.01 to 5 parts by weight per 100 parts by weight of the polylactic acid composition. When the content is less than 0.01 parts by weight, the addition effect of the α-hydroxycarboxylic acid (B) component other than lactic acid does not occur. I can't get it.

The content is preferably selected in the range of 0.01 to 5 parts by weight, more preferably 0.01 to 4 parts by weight, particularly preferably 0.02 to 3 parts by weight.
Specific examples of the α-hydroxycarboxylic acid (B) component other than lactic acid include a glycolic acid component, a 2-hydroxybutyric acid component, a 2-hydroxyvaleric acid component, a 2-hydroxyisovaleric acid component, and 2-hydroxy-4. Examples thereof include α-hydroxycarboxylic acid components (B) other than lactic acid, wherein R ′ in the above formula is an aliphatic group, such as a methyl-valeric acid component.

When obtaining the polylactic acid composition described later, the α-hydroxylcarboxylic acid other than these lactic acids is produced from a cyclic dimer containing these components in the production of the aforementioned poly L-lactic acid and poly D-lactic acid. For example, 2-hydroxybutyric acid cyclic dimer, 2-hydroxyvaleric acid cyclic dimer, 2-hydroxyisovaleric acid cyclic dimer, 2-hydroxy-4-methyl-valeric acid In addition to the cyclic dimer, a combination in which one of these components is different, or a cyclic dimer of 2-hydroxybutyric acid and lactic acid, one of which is composed of lactic acid, can be used.
By using such a starting material, the glass transition point is improved, the thermal decomposability is lowered, the moldability and the dyeability are improved.

<Carbodiimide compound (C)>
In order to achieve the object of the present invention, it is necessary to contain a carbodiimide compound (C) described later in an amount of 0.01 to 10% by weight per 100% by weight of the total amount of the component (A) and the component (B). is there.
If the content is less than 0.01% by weight, the effect of adding a carbodiimide compound cannot be obtained as expected, while if it exceeds 10% by weight, no further effect of addition can be obtained.
The content is preferably in the range of 0.01 to 5% by weight, more preferably 0.01 to 4% by weight, particularly preferably 0.02 to 3% by weight.
The cyclic carbodiimide compound used as the carbodiimide compound (C) has a cyclic structure. The cyclic carbodiimide compound may have a plurality of cyclic structures.

  The cyclic structure has one carbodiimide group (—N═C═N—), and the first nitrogen and the second nitrogen are bonded by a bonding group. One cyclic structure has only one carbodiimide group. For example, when there are a plurality of cyclic structures in the molecule, such as a spiro ring, one cyclic structure bonded to a spiro atom is included in each cyclic structure. Needless to say, the compound may have a plurality of carbodiimide groups as long as it has a carbodiimide group. The number of atoms in the cyclic structure is preferably 8 to 50, more preferably 10 to 30, further preferably 10 to 20, and particularly preferably 10 to 15.

  Here, the number of atoms in the ring structure means the number of atoms that directly constitute the ring structure, and is, for example, 8 for an 8-membered ring and 50 for a 50-membered ring. This is because if the number of atoms in the cyclic structure is smaller than 8, the stability of the cyclic carbodiimide compound is lowered, and it may be difficult to store and use. From the viewpoint of reactivity, there is no particular restriction on the upper limit of the number of ring members, but cyclic carbodiimide compounds having more than 50 atoms are difficult to synthesize, and the cost may increase significantly. From this viewpoint, the number of atoms in the cyclic structure is preferably 10-30, more preferably 10-20, and particularly preferably 10-15.

  The molecular weight of the cyclic carbodiimide compound is preferably 100 to 1,000. If it is lower than 100, the structural stability and volatility of the cyclic carbodiimide compound may be problematic. On the other hand, if it is higher than 1,000, synthesis in a diluting system is required for the production of cyclic carbodiimide, and the yield is lowered, which may cause a problem in cost. From this viewpoint, it is more preferably 100 to 750, and further preferably 250 to 750.

The cyclic structure is a structure represented by the following formula.

  In the formula, Q is a divalent to tetravalent linking group that is an aliphatic group, an alicyclic group, an aromatic group, or a combination thereof, and may contain a hetero atom or a substituent. Two of the valences of this linking group are used to form a cyclic structure. When Q is a trivalent or tetravalent linking group, it is bonded to a polymer or other cyclic structure via a single bond, a double bond, an atom, or an atomic group.

  The linking group is a divalent to tetravalent C 1-20 aliphatic group, a divalent to tetravalent C 3-20 alicyclic group, a divalent to tetravalent C 5-15 aromatic group, or A combination of these is preferred. As the linking group, one having the necessary number of carbon atoms for forming a cyclic structure is selected. Examples of combinations include structures such as an alkylene-arylene group in which an alkylene group and an arylene group are bonded.

  The aliphatic group, alicyclic group, and aromatic group constituting the bonding group may each include a hetero atom and a substituent. A hetero atom refers to O, N, S, P. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group.

In the present invention, examples of the halogen atom include a chlorine atom, a bromine atom, and an iodine atom.
The linking group (Q) is preferably a divalent to tetravalent linking group represented by the following formula (1-1), (1-2) or (1-3).

In the formula, Ar ¹ and Ar ² are each independently a divalent to tetravalent aromatic group having 5 to 15 carbon atoms, and may contain a hetero atom or a substituent.
Examples of the aromatic group include an arylene group having 5 to 15 carbon atoms, an arenetriyl group having 5 to 15 carbon atoms, and an arenetetrayl group having 5 to 15 carbon atoms. Examples of the arylene group (divalent) include a phenylene group and a naphthalenediyl group. Examples of the arenetriyl group (trivalent) include a benzenetriyl group and a naphthalenetriyl group. Examples of the arenetetrayl group (tetravalent) include a benzenetetrayl group and a naphthalenetetrayl group.

  These aromatic groups may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group. These aromatic groups may contain a hetero atom and have a heterocyclic structure. Heteroatoms include O, N, S, and P.

R ¹ and R ² are each independently a divalent or tetravalent aliphatic group having 1 to 20 carbon atoms, a divalent or tetravalent alicyclic group having 3 to 20 carbon atoms, or a combination thereof, or these aliphatic groups. It is a combination of a group, an alicyclic group and a divalent to tetravalent aromatic group having 5 to 15 carbon atoms, and may contain a hetero atom or a substituent.

  Examples of the aliphatic group include an alkylene group having 1 to 20 carbon atoms, an alkanetriyl group having 1 to 20 carbon atoms, and an alkanetetrayl group having 1 to 20 carbon atoms. Examples of the alkylene group include a methylene group, an ethylene group, a propylene group, a butylene group, a pentylene group, a hexylene group, a heptylene group, an octylene group, a nonylene group, a decylene group, a dodecylene group, and a hexadecylene group. As the alkanetriyl group, methanetriyl group, ethanetriyl group, propanetriyl group, butanetriyl group, pentanetriyl group, hexanetriyl group, heptanetriyl group, octanetriyl group, nonanetriyl group, decantriyl group, dodecantriyl group, Examples include a hexadecantriyl group. As alkanetetrayl group, methanetetrayl group, ethanetetrayl group, propanetetrayl group, butanetetrayl group, pentanetetrayl group, hexanetetrayl group, heptanetetrayl group, octanetetrayl group, nonanetetrayl group Decanetetrayl group, dodecanetetrayl group, hexadecanetetrayl group and the like.

  These aliphatic groups may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group. Moreover, these aliphatic groups may contain a hetero atom. Heteroatoms include O, N, S, and P.

  Examples of the alicyclic group include a cycloalkylene group having 3 to 20 carbon atoms, a cycloalkanetriyl group having 3 to 20 carbon atoms, and a cycloalkanetetrayl group having 3 to 20 carbon atoms. Examples of the cycloalkylene group include a cyclopropylene group, a cyclobutylene group, a cyclopentylene group, a cyclohexylene group, a cycloheptylene group, a cyclooctylene group, a cyclononylene group, a cyclodecylene group, a cyclododecylene group, and a cyclohexadecylene group. As the alkanetriyl group, cyclopropanetriyl group, cyclobutanetriyl group, cyclopentanetriyl group, cyclohexanetriyl group, cycloheptanetriyl group, cyclooctanetriyl group, cyclononanetriyl group, cyclodecanetriyl group , Cyclododecanetriyl group, cyclohexadecanetriyl group and the like. As the alkanetetrayl group, cyclopropanetetrayl group, cyclobutanetetrayl group, cyclopentanetetrayl group, cyclohexanetetrayl group, cycloheptanetetrayl group, cyclooctanetetrayl group, cyclononanetetrayl group, cyclodecanetetrayl group Group, cyclododecanetetrayl group, cyclohexadecanetetrayl group and the like.

  These alicyclic groups may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group. Moreover, these alicyclic groups may include a hetero atom and have a heterocyclic structure. Heteroatoms include O, N, S, and P.

  Examples of the aromatic group include an arylene group having 5 to 15 carbon atoms, an arenetriyl group having 5 to 15 carbon atoms, and an arenetetrayl group having 5 to 15 carbon atoms. Examples of the arylene group include a phenylene group and a naphthalenediyl group. Examples of the arenetriyl group (trivalent) include a benzenetriyl group and a naphthalenetriyl group. Examples of the arenetetrayl group (tetravalent) include a benzenetetrayl group and a naphthalenetetrayl group.

These aromatic groups may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group.
Moreover, these aromatic groups may include a hetero atom and have a heterocyclic structure. Heteroatoms include O, N, S, and P.

X ¹ and X ² are each independently a 2 to 4 valent aliphatic group having 1 to 20 carbon atoms, a 2 to 4 valent alicyclic group having 3 to 20 carbon atoms, and a 2 to 4 valent carbon number having 5 to 5 carbon atoms. 15 aromatic groups, or a combination thereof, which may contain heteroatoms and substituents.

  Examples of the aliphatic group include an alkylene group having 1 to 20 carbon atoms, an alkanetriyl group having 1 to 20 carbon atoms, and an alkanetetrayl group having 1 to 20 carbon atoms. Examples of the alkylene group include a methylene group, an ethylene group, a propylene group, a butylene group, a pentylene group, a hexylene group, a heptylene group, an octylene group, a nonylene group, a decylene group, a dodecylene group, and a hexadecylene group. As the alkanetriyl group, methanetriyl group, ethanetriyl group, propanetriyl group, butanetriyl group, pentanetriyl group, hexanetriyl group, heptanetriyl group, octanetriyl group, nonanetriyl group, decantriyl group, dodecantriyl group, Examples include a hexadecantriyl group. As alkanetetrayl group, methanetetrayl group, ethanetetrayl group, propanetetrayl group, butanetetrayl group, pentanetetrayl group, hexanetetrayl group, heptanetetrayl group, octanetetrayl group, nonanetetrayl group Decanetetrayl group, dodecanetetrayl group, hexadecanetetrayl group and the like.

  These aliphatic groups may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group. Moreover, these aliphatic groups may contain a hetero atom. Heteroatoms include O, N, S, and P.

  Examples of the alicyclic group include a cycloalkylene group having 3 to 20 carbon atoms, a cycloalkanetriyl group having 3 to 20 carbon atoms, and a cycloalkanetetrayl group having 3 to 20 carbon atoms. Examples of the cycloalkylene group include a cyclopropylene group, a cyclobutylene group, a cyclopentylene group, a cyclohexylene group, a cycloheptylene group, a cyclooctylene group, a cyclononylene group, a cyclodecylene group, a cyclododecylene group, and a cyclohexadecylene group. As the alkanetriyl group, cyclopropanetriyl group, cyclobutanetriyl group, cyclopentanetriyl group, cyclohexanetriyl group, cycloheptanetriyl group, cyclooctanetriyl group, cyclononanetriyl group, cyclodecanetriyl group , Cyclododecanetriyl group, cyclohexadecanetriyl group and the like. As the alkanetetrayl group, cyclopropanetetrayl group, cyclobutanetetrayl group, cyclopentanetetrayl group, cyclohexanetetrayl group, cycloheptanetetrayl group, cyclooctanetetrayl group, cyclononanetetrayl group, cyclodecanetetrayl group Group, cyclododecanetetrayl group, cyclohexadecanetetrayl group and the like.

  These alicyclic groups may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group. Moreover, these alicyclic groups may include a hetero atom and have a heterocyclic structure. Heteroatoms include O, N, S, and P.

  Examples of the aromatic group include an arylene group having 5 to 15 carbon atoms, an arenetriyl group having 5 to 15 carbon atoms, and an arenetetrayl group having 5 to 15 carbon atoms. Examples of the arylene group include a phenylene group and a naphthalenediyl group. Examples of the arenetriyl group (trivalent) include a benzenetriyl group and a naphthalenetriyl group. Examples of the arenetetrayl group (tetravalent) include a benzenetetrayl group and a naphthalenetetrayl group.

  These aromatic groups may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group. Moreover, these aromatic groups may include a hetero atom and have a heterocyclic structure. Heteroatoms include O, N, S, and P.

s and k are each independently an integer of 0 to 10, preferably an integer of 0 to 3, more preferably an integer of 0 to 1. When s and k exceed 10, the cyclic carbodiimide compound is difficult to synthesize, and the cost may increase significantly. From this viewpoint, the integer is preferably selected in the range of 0 to 3. When s or k is 2 or more, X ¹ or X ² as a repeating unit may be different from other X ¹ or X ² .

X ³ is a 2 to 4 valent aliphatic group having 1 to 20 carbon atoms, a 2 to 4 valent alicyclic group having 3 to 20 carbon atoms, a 2 to 4 valent aromatic group having 5 to 15 carbon atoms, Or it is a combination of these and may contain a hetero atom and a substituent.

  Examples of the aliphatic group include an alkylene group having 1 to 20 carbon atoms, an alkanetriyl group having 1 to 20 carbon atoms, and an alkanetetrayl group having 1 to 20 carbon atoms. Examples of the alkylene group include a methylene group, an ethylene group, a propylene group, a butylene group, a pentylene group, a hexylene group, a heptylene group, an octylene group, a nonylene group, a decylene group, a dodecylene group, and a hexadecylene group. As the alkanetriyl group, methanetriyl group, ethanetriyl group, propanetriyl group, butanetriyl group, pentanetriyl group, hexanetriyl group, heptanetriyl group, octanetriyl group, nonanetriyl group, decantriyl group, dodecantriyl group, Examples include a hexadecantriyl group. As alkanetetrayl group, methanetetrayl group, ethanetetrayl group, propanetetrayl group, butanetetrayl group, pentanetetrayl group, hexanetetrayl group, heptanetetrayl group, octanetetrayl group, nonanetetrayl group Decanetetrayl group, dodecanetetrayl group, hexadecanetetrayl group and the like.

  These aliphatic groups may contain a substituent, such as an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, or an ester group. , Ether group, aldehyde group and the like. Moreover, these aliphatic groups may contain a hetero atom. Heteroatoms include O, N, S, and P.

  Examples of the alicyclic group include a cycloalkylene group having 3 to 20 carbon atoms, a cycloalkanetriyl group having 3 to 20 carbon atoms, and a cycloalkanetetrayl group having 3 to 20 carbon atoms. Examples of the cycloalkylene group include a cyclopropylene group, a cyclobutylene group, a cyclopentylene group, a cyclohexylene group, a cycloheptylene group, a cyclooctylene group, a cyclononylene group, a cyclodecylene group, a cyclododecylene group, and a cyclohexadecylene group. As the alkanetriyl group, cyclopropanetriyl group, cyclobutanetriyl group, cyclopentanetriyl group, cyclohexanetriyl group, cycloheptanetriyl group, cyclooctanetriyl group, cyclononanetriyl group, cyclodecanetriyl group , Cyclododecanetriyl group, cyclohexadecanetriyl group and the like. As the alkanetetrayl group, cyclopropanetetrayl group, cyclobutanetetrayl group, cyclopentanetetrayl group, cyclohexanetetrayl group, cycloheptanetetrayl group, cyclooctanetetrayl group, cyclononanetetrayl group, cyclodecanetetrayl group Group, cyclododecanetetrayl group, cyclohexadecanetetrayl group and the like.

  These alicyclic groups may contain a substituent, such as an alkyl group having 1 to 20 carbon atoms, an arylene group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, and an ester. Group, ether group, aldehyde group and the like. Moreover, these alicyclic groups may include a hetero atom and have a heterocyclic structure. Heteroatoms include O, N, S, and P.

  Examples of the aromatic group include an arylene group having 5 to 15 carbon atoms, an arenetriyl group having 5 to 15 carbon atoms, and an arenetetrayl group having 5 to 15 carbon atoms. Examples of the arylene group include a phenylene group and a naphthalenediyl group. Examples of the arenetriyl group (trivalent) include a benzenetriyl group and a naphthalenetriyl group. Examples of the arenetetrayl group (tetravalent) include a benzenetetrayl group and a naphthalenetetrayl group.

  These aromatic groups may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 15 carbon atoms, a halogen atom, a nitro group, an amide group, a hydroxyl group, an ester group, an ether group, and an aldehyde group. Moreover, these aromatic groups may include a hetero atom and have a heterocyclic structure. Heteroatoms include O, N, S, and P.

As described above, Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² and X ³ may contain a hetero atom.
When Q is a divalent linking group, Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² and X ³ are all divalent groups. When Q is a trivalent linking group, one of Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² and X ³ is a trivalent group. When Q is a tetravalent linking group, one of Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² and X ³ is a tetravalent group or two are trivalent It is a group.

  Examples of the cyclic carbodiimide used in the present invention include compounds represented by the following (a) to (c).

<Cyclic carbodiimide (a)>
Examples of the cyclic carbodiimide used in the present invention include a compound represented by the following formula (2) (hereinafter sometimes referred to as “cyclic carbodiimide (a)”).

In the formula, Q _a is a divalent linking group that is an aliphatic group, an alicyclic group, an aromatic group, or a combination thereof, and may contain a hetero atom or a substituent.
The aliphatic group, alicyclic group, and aromatic group are the same as those described in Formula (1). However, in the compound of formula (2), the aliphatic group, alicyclic group, and aromatic group are all divalent. Q _a is preferably a divalent linking group represented by the following formula (2-1), (2-2) or (2-3).

In the formula, Ar _a ¹ , Ar _a ² , R _a ¹ , R _a ² , X _a ¹ , X _a ² , X _a ³ , s and k are represented by formulas (1-1) to (1-3), respectively. Are the same as Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² , X ³ , s and k. However, these are all divalent.
As the cyclic carbodiimide (a), a compound represented by the following formula (2-1-1) is preferable.

_{Wherein, X} ^{a 1} is preferably 1 to 20 carbon atoms, more preferably an alkylene group having 1 to 10 carbon atoms. Examples of the alkylene group include a methylene group, an ethylene group, a trimethylene group, and a tetramethylene group.
In the formula, Ar _a ¹ and Ar _a ² are each independently an arylene group having 5 to 15 carbon atoms which may be substituted. Examples of the arylene group include a phenylene group and a naphthalenediyl group. The arylene group may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, preferably 1 to 6 carbon atoms. Examples of the substituent include a methyl group, an ethyl group, and a propyl group.
As the cyclic carbodiimide (a), a compound represented by the following formula (2-1-1a) is preferable.

_{Wherein, X} ^{a 1} is preferably 1 to 20 carbon atoms, more preferably 1 to 10 carbon atoms, more preferably an alkylene group having 1 to 4 carbon atoms. Examples of the alkylene group include a methylene group, an ethylene group, a trimethylene group, and a tetramethylene group.
In the formula, R ^q and R ^r are each independently preferably an alkyl group having 1 to 20 carbon atoms, more preferably an alkyl group having 1 to 6 carbon atoms or a hydrogen atom. Examples of the alkyl group include a methyl group, an ethyl group, and a propyl group.
Examples of the cyclic carbodiimide compound (a) include the following compounds.

<Cyclic carbodiimide (b)>
Furthermore, examples of the cyclic carbodiimide used in the present invention include a compound represented by the following formula (3) (hereinafter sometimes referred to as “cyclic carbodiimide (b)”).

Wherein, Q _b is an aliphatic group, an alicyclic group, an aromatic group or a trivalent linking group combinations thereof, a hetero atom may contain substituents. Y is a carrier supporting a cyclic structure. The aliphatic group, alicyclic group, and aromatic group are the same as those described in Formula (1). However, in the compound of formula (3), the inner one of the group constituting the Q _b is trivalent.
Q _b is preferably a trivalent linking group represented by the following formula (3-1), (3-2) or (3-3).

In the formula, Ar _b ¹ , Ar _b ² , R _b ¹ , R _b ² , X _b ¹ , X _b ² , X _b ³ , s and k are respectively represented by the formulas (1-1) to (1-3). The same as Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² , X ³ , s and k. However, one of these is a trivalent group.
Y is preferably a single bond, a double bond, an atom, an atomic group or a polymer. Y is a bonding portion, and a plurality of cyclic structures are bonded via Y to form a structure represented by the formula (3).
Examples of the cyclic carbodiimide compound (b) include the following compounds.

<Cyclic carbodiimide (c)>
Examples of the cyclic carbodiimide used in the present invention include a compound represented by the following formula (4) (hereinafter sometimes referred to as “cyclic carbodiimide (c)”).

In the formula, Q _c is a tetravalent linking group that is an aliphatic group, an alicyclic group, an aromatic group, or a combination thereof, and may contain a hetero atom or a substituent. Z ¹ and Z ² are carriers that support a cyclic structure. Z ¹ and Z ² may be bonded to each other to form a cyclic structure.
The aliphatic group, alicyclic group, and aromatic group are the same as those described in Formula (1). However, in the compound of formula (4), Q _c is tetravalent. Accordingly, one of these groups is a tetravalent group or two are trivalent groups.
Q _c is preferably a tetravalent linking group represented by the following formula (4-1), (4-2) or (4-3).

Ar _c ¹ , Ar _c ² , R _c ¹ , R _c ² , X _c ¹ , X _c ² , X _c ³ , s and k are each Ar ^{1 in} formulas (1-1) to (1-3). , Ar ² , R ¹ , R ² , X ¹ , X ² , X ³ , s and k are the same. Provided that Ar _c ¹ , Ar _c ² , R _c ¹ , R _c ² , X _c ¹ , X _c ² and X _c ³ are one of which is a tetravalent group or two of which are trivalent It is a group.
Z ¹ and Z ² are preferably each independently a single bond, a double bond, an atom, an atomic group or a polymer. Z ¹ and Z ² are bonding portions, and a plurality of cyclic structures are bonded via Z ¹ and Z ² to form a structure represented by the formula (4).
As the cyclic carbodiimide compound (c), a compound represented by the following formula (4-1-1) is preferable.

_{Wherein, X} ^{c 1} is preferably 1 to 20 carbon atoms, more preferably 1 to 10 carbon atoms, more preferably alkanetetrayl group having 1 to 6 carbon atoms. Examples of the alkanetetrayl group include an isobutanetetrayl group, an isopentanetetrayl group, and a neopentanetetrayl group. A neopentanetetrayl group represented by the following formula is preferred.

In the formula, Ar _c ¹ , Ar _c ² , Ar _c ³ , and Ar _c ⁴ are each an independently substituted arylene group having 5 to 15 carbon atoms. Examples of the arylene group include a phenylene group and a naphthalenediyl group. The arylene group may be substituted. Examples of the substituent include an alkyl group having 1 to 20 carbon atoms, preferably 1 to 6 carbon atoms. Examples of the substituent include a methyl group, an ethyl group, and a propyl group.
As the cyclic carbodiimide (c), a compound represented by the following formula (2-1-1c) is preferable.

_{Wherein, X} ^{c 1} is preferably 1 to 20 carbon atoms, more preferably 1 to 10 carbon atoms, more preferably alkanetetrayl group having 1 to 6 carbon atoms. Examples of the alkanetetrayl group include an isobutanetetrayl group, an isopentanetetrayl group, and a neopentanetetrayl group. A neopentanetetrayl group represented by the following formula is preferred.

In the formula, R ^q , R ^r , R ^s , and R ^t are each independently an alkyl group having 1 to 20 carbon atoms, preferably an alkyl group having 1 to 6 carbon atoms, or a hydrogen atom. Examples of the alkyl group include a methyl group, an ethyl group, and a propyl group.
Examples of the cyclic carbodiimide compound (c) include the following compounds.

<Method for producing cyclic carbodiimide compound>
In the present invention, the production method of the cyclic carbodiimide compound is not particularly limited and can be produced by a conventionally known method. For example, a method for producing an amine body via an isocyanate body, a method for producing an amine body via an isothiocyanate body, a method for producing an amine body via a triphenylphosphine body, a urea body from an amine body The method of manufacturing via a thiourea body, the method of manufacturing via a thiourea body, the method of manufacturing from a carboxylic acid body via an isocyanate body, the method of manufacturing a lactam body, etc. are mentioned.

  Moreover, the cyclic carbodiimide compound of this invention can be manufactured by combining the method described in the following literature, or changing or combining suitably according to the target compound.

Tetrahedron Letters, Vol. 34, no. 32, 515-5158, 1993.
Medium- and Large-Membered Rings from Bis (iminophosphoranes): An Efficient Preparation of Cyclic Carbidiimides, Pedro Molina et al.
Journal of Organic Chemistry, Vol. 61, no. 13, 4289-4299, 1996.
New Models for the Study of the Racemization Mechanism of Carbodiimides. Synthesis and Structure (X-ray Crystallography and 1H NMR) of Cyclic Carbodiimides, Pedro Molina et al.
Journal of Organic Chemistry, Vol. 43, No8, 1944-1946, 1978.
Macrocyclic Ureas As Masked Isocynates, Henri Ulrich et al.
Journal of Organic Chemistry, Vol. 48, no. 10, 1694-1700, 1983.
Synthesis and Reactions of Cyclic Carbodiimides, R.A. Richter et al.
Journal of Organic Chemistry, Vol. 59, no. 24, 7306-7315, 1994.
A New and Efficient Preparation of Cyclic Carboxidimids from Bis (iminophosphoranea) and the System Boc2O / DMAP, Pedro Molina et al.

（２）得られたニトロ体を還元して下記式（ｄ）で表わされるアミン体を得る工程、

（３）得られたアミン体とトリフェニルホスフィンジブロミドを反応させ下記式（ｅ）で表されるトリフェニルホスフィン体を得る工程、および

（４）得られたトリフェニルホスフィン体を反応系中でイソシアネート化した後、直接脱炭酸させることによって製造したものは、本願発明に用いる環状カルボジイミド化合物として好適に用いることができる。
（上記式中、Ａｒ^１およびＡｒ^２は各々独立に、炭素数１〜６のアルキル基またはフェニル基で置換されていてもよい芳香族基である。Ｅ^１およびＥ^２は各々独立に、ハロゲン原子、トルエンスルホニルオキシ基およびメタンスルホニルオキシ基、ベンゼンスルホニルオキシ基、ｐ−ブロモベンゼンスルホニルオキシ基からなる群から選ばれる基である。Ａｒ_ａは、フェニル基である。Ｘは、下記式（ｉ−１）から（ｉ−３）の結合基である。） Depending on the compound to be produced, an appropriate production method may be employed. For example, (1) nitrophenols represented by the following formula (a-1), nitrophenols represented by the following formula (a-2) And a compound represented by the following formula (b) to obtain a nitro compound represented by the following formula (c),

(2) A step of reducing the obtained nitro body to obtain an amine body represented by the following formula (d);

(3) a step of reacting the obtained amine body with triphenylphosphine dibromide to obtain a triphenylphosphine body represented by the following formula (e); and

(4) After the obtained triphenylphosphine body is isocyanated in the reaction system and then directly decarboxylated, it can be suitably used as the cyclic carbodiimide compound used in the present invention.
(In the above formula, Ar ¹ and Ar ² are each independently an aromatic group optionally substituted with an alkyl group having 1 to 6 carbon atoms or a phenyl group. E ¹ and E ² are each independently a halogen atom. A group selected from the group consisting of an atom, a toluenesulfonyloxy group, a methanesulfonyloxy group, a benzenesulfonyloxy group, and a p-bromobenzenesulfonyloxy group, Ar _a is a phenyl group, X is represented by the following formula (i -1) to (i-3).

<Polylactic acid composition>
In the polylactic acid composition of the present invention, the polylactic acid (A) component is 95% by weight or more and 99.99% by weight or less based on the composition, and the α-hydroxycarboxylic acid (B) component other than lactic acid is 0.01%. The carbodiimide compound (C) is contained in an amount of 0.01 to 10% by weight per 100% by weight of the total amount of the component (A) and the component (B).
The polylactic acid (A) component and the α-hydroxycarboxylic acid (B) component other than lactic acid are as described above.

  The polylactic acid composition of the present invention preferably has a lactide content of 1 to 5000 (wtppm). The lactide contained in the polylactic acid composition deteriorates the polylactic acid composition and deteriorates the color tone at the time of melt processing, and may be rendered unusable as a product.

  Poly L-lactic acid and / or poly D-lactic acid immediately after the melt ring-opening polymerization usually contains 1 to 5% by weight of lactide, but poly L-lactic acid and / or poly D-lactic acid is polymerized from the end of polymerization. At any stage up to the formation of the lactic acid composition, a conventionally known lactide weight loss method, that is, a vacuum devolatilization method in a single-screw or multi-screw extruder, or a high vacuum treatment in a polymerization apparatus is used alone or in combination. In practice, lactide can be reduced to a suitable range.

  The smaller the lactide content, the better the melt stability and heat-and-moisture resistance stability of the polylactic acid composition, but there is also an advantage of lowering the polylactic acid composition melt viscosity. Reasonable and economical. That is, it is reasonable to set it to 1 to 1000 (wtppm) at which practical melt stability is achieved. More preferably, a range of 1 to 700 (wtppm), more preferably 2 to 500 (wtppm), and particularly preferably 5 to 100 (wtppm) is selected.

  Since the polylactic acid composition has a lactide content in such a range, the stability of the polylactic acid composition of the present invention at the time of melt molding can be improved, and the molded product can be efficiently manufactured and the heat resistance of the molded product Stability and low gas properties can be improved.

  A polylactic acid composition containing a stereocomplex phase polylactic acid is obtained by bringing a poly L-lactic acid component and a poly D-lactic acid component into contact with each other in a weight ratio of 10/90 to 90/10, preferably by melt-contacting. More preferably, it can be obtained by contact with melt kneading.

  The contact temperature is selected in the range of 220 to 290 ° C., preferably 220 to 280 ° C., and more preferably 225 to 275 ° C. from the viewpoint of improving the stability of polylactic acid when melted and the stereocomplex crystallinity.

  The melt kneading method is not particularly limited, but a conventionally known batch type or continuous type melt mixing apparatus is preferably used. For example, melt stirring tank, single-screw or twin-screw extruder, kneader, non-shaft vertical stirring tank (finisher), Violac made by Sumitomo Heavy Industries, N-SCR made by Mitsubishi Heavy Industries, glasses blade made by Hitachi, lattice blade or Kenix type stirrer Alternatively, a Sulzer-type SMLX type static mixer equipped pipe type polymerization apparatus can be used, but a non-axial vertical stirring tank, N-SCR, which is a self-cleaning type polymerization apparatus in terms of productivity, quality of polylactic acid, especially color tone A biaxial extrusion ruder or the like is preferably used.

  In the polylactic acid composition of the present invention, in order to stably and highly advance the formation of a complex phase, it is essential to apply a component having an acid value of less than 5 as a stereocomplex crystallization accelerator. ) And (iii) are preferably selected. Such phosphoric acid ester metal salts can be used alone or in combination.

In the formula, R ¹¹ represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, R ¹² and R ¹³ each independently represents a hydrogen atom or an alkyl group having 1 to 12 carbon atoms, and M ₁ represents Represents an alkali metal atom, an alkaline earth metal atom, a zinc atom or an aluminum atom, p represents 1 or 2, q represents 0 when M ₁ is an alkali metal atom, an alkaline earth metal atom or a zinc atom; When it is an atom, it represents 1 or 2.

In the formula, each of R ¹⁴ , R ¹⁵ and R ¹⁶ independently represents a hydrogen atom or an alkyl group having 1 to 12 carbon atoms, and M ₂ represents an alkali metal atom, an alkaline earth metal atom, a zinc atom or an aluminum atom. P represents 1 or 2, q represents 0 when M ₂ is an alkali metal atom, alkaline earth metal atom or zinc atom, and 1 or 2 when M ₂ is an aluminum atom.

M ₁ and M ₂ of the metal phosphate represented by the above two formulas are preferably Na, K, Al, Mg, Ca and Li, and in particular, Li, Al is the most among K, Na, Al and Li. It can be used suitably.
Among them, trade names “ADEKA STAB” NA-10, NA-11, NA-21, NA-30, NA-35, NA-71 and the like manufactured by ADEKA Corporation are exemplified as suitable agents.

  With respect to the polylactic acid composition, the phosphoric acid ester metal salt is 0.001 to 2 wt%, preferably 0.005 to 1 wt%, more preferably 0.01 to 0.5 wt%, and further preferably 0.02 to 0.2 wt%. It is preferable to use 3 wt%. When the amount is too small, the effect of improving the degree of crystallinity of the stereocomplex is small, and when too large, the stereocomplex phase melting point is lowered, which is not preferable.

Furthermore, if desired, a known crystallization nucleating agent described below can be used in combination in order to enhance the action of the metal phosphate within the scope not departing from the gist of the present invention. Of these, calcium silicate, talc, kaolinite, and montmorillonite are preferably selected.
The amount of the crystallization nucleating agent used is selected in the range of 0.05 to 5 wt%, more preferably 0.06 to 2 wt%, still more preferably 0.06 to 1 wt% with respect to the polylactic acid composition.

  In the present invention, in order to further increase the degree of stereocomplex crystallinity of polylactic acid, [(epoxy group, oxazoline group, oxazine group, isocyanate group, ketene group and carbodiimide group) (hereinafter abbreviated as a specific functional group) as a stereocomplex crystallization aid. It is preferable to add a compound having at least one functional group selected from the group of

  Stereocomplex crystallizing aid is a specific functional group that reacts with the molecular terminal of polylactic acid composition to partially link poly L-lactic acid unit and poly D-lactic acid unit to promote stereocomplex phase formation. It is the agent that the present inventors speculate that it is made to be.

  As the stereocomplex crystallization aid, a known agent can be suitably applied as a carboxyl group-capping agent for conventional polyesters described below. Of these, known carbodiimide compounds, oxazoline compounds and the like are suitably selected in the present invention because of the effect of promoting the formation of complex phases and the hue of the composition.

  Of the stereocomplex crystallization aids, agents containing oxazine groups, isocyanate groups, and carbodiimide groups cause deterioration of the working environment due to malodor due to thermal decomposition of the agent during the formation of the complex phase, and deterioration of the color tone of the polylactic acid composition. Because there is a high risk of causing it, it is preferable to prepare a separate work environment for use. When using it, it is limited to the case where emphasis is placed on the formation of a complex phase height, and it should be used as little as possible. It is preferable to do.

  In addition, agents with only ketene groups and epoxy groups are less concerned about deterioration of the working environment, but the application of these agents should be avoided because the effect of deterioration of the hue of the polylactic acid composition composition is similar to or greater than that of carbodiimide compounds. Is preferred.

  The amount of the stereocomplex crystallization aid used is not more than 1 wt%, preferably 0 to 0.5 wt%, more preferably 0 to 0.3 wt%, still more preferably 0 to 0.1 wt% in the same standard as above. Is selected.

In the present invention, the carboxyl end group concentration of the polylactic acid composition is 0.01 to 10 (equivalent / 10 ⁶ g), and {hereinafter (equivalent / 10 ⁶ g) may be abbreviated as (eq / ton). } Is preferred. A range of 0.02 to 5 (eq / ton) is more preferable, and a range of 0.5 to 3 (eq / ton) is more preferably selected.

  When the carboxyl end group concentration is within this range, the polylactic acid composition of the present invention and the molded article of the present invention comprising this composition can have good heat resistance, hue, and particularly heat and humidity resistance.

In order to reduce the carboxyl end group concentration of the polylactic acid composition to 10 (eq / ton) or less, conventionally known methods for reducing the carboxyl end group concentration in the polyester composition can be suitably applied. For example, it is also possible to esterify or amidate with an alcohol or amine without adding a conventionally known end capping agent or without adding such a terminal capping agent.
As such an end-capping agent, the stereocomplex crystallization aid having the specific functional group described above can effectively seal the carboxyl group.

  Examples of the epoxy compound that can be used as a stereocomplex crystallization aid having a specific functional group in the present invention include glycidyl ether compounds, glycidyl ester compounds, glycidyl amine compounds, glycidyl imide compounds, glycidyl amide compounds, and alicyclic epoxy compounds. Can be preferably used. By blending such an agent, formation of a complex phase of the polylactic acid composition can be promoted, and a polylactic acid molded product having excellent mechanical properties, heat resistance, moist heat resistance, durability, moldability, and the like can be obtained.

  Examples of glycidyl ether compounds include, for example, stearyl glycidyl ether, phenyl glycidyl ether, ethylene oxide lauryl alcohol glycidyl ether, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, neopentylene glycol diglycidyl ether, Bisphenol A obtained by condensation reaction of epichlorohydrin with polytetramethylene glycol diglycidyl ether, glycerol triglycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol tetraglycidyl ether, and other bisphenols such as bis (4-hydroxyphenyl) methane Diglycidyl ether type epoxy resin Etc. can be mentioned, among others bisphenol A diglycidyl ether type epoxy resin is preferable. Examples of glycidyl ester compounds include, for example, glycidyl benzoate, glycidyl stearate, glycidyl stearic acid, diglycidyl terephthalate, diglycidyl phthalate, diglycidyl phthalate dicarboxylate, diglycidyl adipate, Examples include acid diglycidyl ester, dodecanedioic acid diglycidyl ester, pyromellitic acid tetraglycidyl ester, and the like. Among them, benzoic acid glycidyl ester and versatic acid glycidyl ester are preferable.

  Examples of the glycidylamine compound include tetraglycidylamine diphenylmethane, triglycidyl-p-aminophenol, diglycidylaniline, diglycidyltoluidine, tetraglycidylmetaxylenediamine, triglycidyl isocyanurate, and the like.

  Examples of glycidyl imide and glycidyl amide compounds include N-glycidyl phthalimide, N-glycidyl-4,5-dimethyl phthalimide, N-glycidyl-3,6-dimethyl phthalimide, N-glycidyl succinimide, N-glycidyl-1 , 2,3,4-tetrahydrophthalimide, N-glycidyl maleimide, N-glycidyl benzamide, N-glycidyl stearyl amide, etc., among which N-glycidyl phthalimide is preferable.

  Examples of alicyclic epoxy compounds include 3,4-epoxycyclohexyl-3,4-cyclohexylcarboxylate, bis (3,4-epoxycyclohexylmethyl) adipate, vinylcyclohexene diepoxide, N-methyl-4,5- Examples thereof include epoxycyclohexane-1,2-dicarboxylic imide, N-phenyl-4,5-epoxycyclohexane-1,2-dicarboxylic imide and the like. Furthermore, a polyepoxy compound containing the above compound as a monomer unit, particularly a polyepoxy compound having an epoxy group as a pendant group in a side chain, and the like can be mentioned as suitable agents.

  As other epoxy compounds, epoxy-modified fatty acid glycerides such as epoxidized soybean oil, epoxidized linseed oil, and epoxidized whale oil, phenol novolac type epoxy resins, cresol novolac type epoxy resins and the like can be used.

  Examples of oxazoline compounds that can be used as a stereocomplex crystallization aid having a specific functional group used in the present invention include 2-methoxy-2-oxazoline, 2-butoxy-2-oxazoline, and 2-stearyloxy-2-oxazoline. 2-cyclohexyloxy-2-oxazoline, 2-allyloxy-2-oxazoline, 2-benzyloxy-2-oxazoline, 2-p-phenylphenoxy-2-oxazoline, 2-methyl-2-oxazoline, 2-cyclohexyl- 2-oxazoline, 2-methallyl-2-oxazoline, 2-crotyl-2-oxazoline, 2-phenyl-2-oxazoline, 2-o-ethylphenyl-2-oxazoline, 2-o-propylphenyl-2-oxazoline, 2-p-phenylphenyl-2 Oxazoline, 2,2'-bis (2-oxazoline), 2,2'-bis (4-methyl-2-oxazoline) 2,2'-bis (4-butyl-2-oxazoline), 2,2'- m-phenylenebis (2-oxazoline), 2,2′-p-phenylenebis (4-methyl-2-oxazoline), 2,2′-p-phenylenebis (4,4′-methyl-2-oxazoline) 2,2′-ethylenebis (2-oxazoline), 2,2′-tetramethylenebis (2-oxazoline), 2,2′-hexamethylenebis (2-oxazoline), 2,2′-ethylenebis ( 4-methyl-2-oxazoline), 2,2′-tetramethylenebis (4,4′-dimethyl-2-oxazoline), 2,2′-cyclohexylenebis (2-oxazoline), 2,2′-dipheni Nbisu (4-methyl-2-oxazoline), and the like more specific oxazoline resin of the present invention.

  Among the oxazoline compounds, 2,2'-m-phenylenebis (2-oxazoline), 2,2'-p-phenylenebis (2-oxazoline) and the specific oxazoline resin of the present invention are selected as preferred.

  Examples of oxazine compounds that can be used as a stereocomplex crystallization aid having a specific functional group in the present invention include 2-methoxy-5,6-dihydro-4H-1,3-oxazine, 2-hexyloxy-5. , 6-dihydro-4H-1,3-oxazine, 2-decyloxy-5,6-dihydro-4H-1,3-oxazine, 2-cyclohexyloxy-5,6-dihydro-4H-1,3-oxazine, Examples include 2-allyloxy-5,6-dihydro-4H-1,3-oxazine, 2-crotyloxy-5,6-dihydro-4H-1,3-oxazine and the like.

  Further, 2,2′-bis (5,6-dihydro-4H-1,3-oxazine), 2,2′-methylenebis (5,6-dihydro-4H-1,3-oxazine), 2,2′- Ethylenebis (5,6-dihydro-4H-1,3-oxazine), 2,2′-hexamethylenebis (5,6-dihydro-4H-1,3-oxazine), 2,2′-p-phenylene Bis (5,6-dihydro-4H-1,3-oxazine), 2,2′-P, P′-diphenylenebis (5,6-dihydro-4H-1,3-oxazine) and the like can be mentioned.

  Furthermore, a polyoxazine compound containing the above-described compound as a monomer unit, particularly a polyoxazine compound having the above functional group as a pendant group in a side chain, and the like can be mentioned as suitable agents.

  Examples of isocyanate compounds that can be used in the present invention include aromatic isocyanates, aliphatic isocyanates, alicyclic isocyanate compounds, and mixtures thereof.

  Examples of the monoisocyanate compound that can be used as a stereocomplex crystallization aid having a specific functional group include phenyl isocyanate, tolyl isocyanate, dimethylphenyl isocyanate, cyclohexyl isocyanate, butyl isocyanate, and naphthyl isocyanate.

Specific examples of the diisocyanate include 4,4′-diphenylmethane diisocyanate, 4,4′-diphenyldimethylmethane diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, (2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate) mixture, cyclohexane-4,4′-diisocyanate, xylylene diisocyanate, isophorone diisocyanate, dicyclohexylmethane 4,4 '-Diisocyanate, methylcyclohexane diisocyanate, tetramethylxylylene diisocyanate, 2,6-diisopropylphenyl-1,4-diisocyanate, etc. it can.
Among these isocyanate compounds, aromatic isocyanates such as 4,4′-diphenylmethane diisocyanate and phenyl isocyanate are preferable.

  Examples of ketene compounds that can be used as stereocomplex crystallization aids having specific functional groups include aromatic ketene compounds, aliphatic ketene compounds, alicyclic ketene compounds, and mixtures thereof.

  Specific examples of the compound include diphenyl ketene, bis (2,6-di-tert-butylphenyl) ketene, bis (2,6-di-isopropylphenyl) ketene, and dicyclohexyl ketene.

  Among these ketene compounds, aromatic ketenes such as diphenyl ketene, bis (2,6-di-tert-butylphenyl) ketene, and bis (2,6-di-isopropylphenyl) ketene are preferable.

  As the agent that can be used as the stereocomplex crystallization aid and the end-capping agent, one or more compounds can be appropriately selected and used. One of preferred embodiments is to promote formation of a complex phase with a stereocomplex crystallization aid and to seal a carboxyl group terminal and a part of an acidic low molecular weight compound.

  The polylactic acid composition of the present invention includes a thermoplastic resin other than polylactic acid, a stabilizer, a crystallization accelerator, a filler, a mold release agent, an antistatic agent, a carboxyl group reaction, as long as it does not contradict the gist of the present invention. At least one selected from the group consisting of a conductive end-capping agent, a plasticizer, an impact stabilizer and the like.

<Thermoplastic resin>
The polylactic acid composition of the present invention can contain a thermoplastic resin other than the polylactic acid composition of the present invention. Examples of such thermoplastic resins include polyester resins other than polylactic acid, polyamide resins, polyacetal resins, polyolefin resins such as polyethylene resins and polypropylene resins, polystyrene resins, acrylic resins, polyurethane resins, chlorinated polyethylene resins, and chlorinated polypropylene resins. , Aromatic and aliphatic polyketone resins, fluorine resins, polyphenylene sulfide resins, polyether ether ketone resins, polyimide resins, thermoplastic starch resins, AS resins, ABS resins, AES resins, ACS resins, polyvinyl chloride resins, poly Vinylidene chloride resin, vinyl ester resin, MS resin, polycarbonate resin, polyarylate resin, polysulfone resin, polyethersulfone resin, phenoxy resin, polyphenylene oxide Fat, poly-4-methylpentene-1, polyetherimide resin, cellulose acetate resin, and thermoplastic resins such as polyvinyl alcohol resins.

Among them, selected from polyacetal resins, polyester resins other than polylactic acid, for example, polyester resins such as PET (polyethylene terephthalate), PTT (polytrimethylene terephthalate), PBT (polybutylene terephthalate), PEN (polyethylene naphthalate), and polyamide resins. It is preferable to blend at least one kind.
By blending these resins, the surface properties, moldability, mechanical properties, durability, toughness and the like of the molded article made of the composition of the present invention can be made excellent.

  The content of the thermoplastic resin is preferably 0.5 to 200 parts by weight, more preferably 1 to 100 parts by weight, further preferably 3 to 70 parts by weight, based on 100 parts by weight of the polylactic acid composition of the present invention. More preferably, it is 5 to 50 parts by weight. By blending these resins, a composition and a molded product having excellent characteristics can be obtained.

<Stabilizer>
The polylactic acid composition of the present invention can contain a stabilizer. As a stabilizer, what is used for the stabilizer of a normal thermoplastic resin can be used. For example, an antioxidant, a light stabilizer, etc. can be mentioned. By blending these agents, a molded product having excellent mechanical properties, moldability, heat resistance and durability can be obtained.

  Examples of the antioxidant include hindered phenol compounds, hindered amine compounds, phosphite compounds, thioether compounds, and the like.

  Examples of hindered phenol compounds include n-octadecyl-3- (3 ′, 5′-di-tert-butyl-4′-hydroxyphenyl) -propionate, n-octadecyl-3- (3′-methyl-5 ′). -Tert-butyl-4'-hydroxyphenyl) -propionate, n-tetradecyl-3- (3 ', 5'-di-tert-butyl-4'-hydroxyphenyl) -propionate, 1,6-hexanediol- Bis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) -propionate], 1,4-butanediol-bis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) ) -Propionate], 2,2′-methylene-bis (4-methyl-tert-butylphenol), triethylene glycol-bis 3- (3-tert-butyl-5-methyl-4-hydroxyphenyl) -propionate], tetrakis [methylene-3- (3 ′, 5′-di-tert-butyl-4-hydroxyphenyl) propionate] methane, 3,9-bis [2- {3- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionyloxy} -1,1-dimethylethyl] 2,4,8,10-tetraoxaspiro ( 5,5) Undecane and the like can be mentioned.

  As a hindered amine compound, N, N′-bis-3- (3 ′, 5′-di-tert-butyl-4′-hydroxyphenyl) propionylhexamethylenediamine, N, N′-tetramethylene-bis [3- (3′-Methyl-5′-tert-butyl-4′-hydroxyphenyl) propionyl] diamine, N, N′-bis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) -propionyl ] Hydrazine, N-salicyloyl-N'-salicylidenehydrazine, 3- (N-salicyloyl) amino-1,2,4-triazole, N, N'-bis [2- {3- (3,5-di -Tert-butyl-4-hydroxyphenyl) propionyloxy} ethyl] oxyamide and the like. Preferably, triethylene glycol-bis [3- (3-tert-butyl-5-methyl-4-hydroxyphenyl) -propionate] and tetrakis [methylene-3- (3 ′, 5′-di-tert-butyl) -4-hydroxyphenyl) propionate] methane and the like.

  As the phosphite compound, those in which at least one P—O bond is bonded to an aromatic group are preferable. Specifically, tris (2,6-di-tert-butylphenyl) phosphite, tetrakis ( 2,6-di-tert-butylphenyl) 4,4′-biphenylene phosphite, bis (2,6-di-tert-butyl-4-methylphenyl) pentaerythritol-di-phosphite, 2,2-methylenebis (4,6-di-tert-butylphenyl) octyl phosphite, 4,4′-butylidene-bis (3-methyl-6-tert-butylphenyl-di-tridecyl) phosphite, 1,1,3-tris (2-methyl-4-ditridecyl phosphite-5-tert-butylphenyl) butane, tris (mixed mono and di-no Butylphenyl) phosphite, tris (nonylphenyl) phosphite, 4,4'-isopropylidene-bis (phenyl - dialkyl phosphite), and the like.

  Among them, tris (2,6-di-tert-butylphenyl) phosphite, 2,2-methylenebis (4,6-di-tert-butylphenyl) octyl phosphite, bis (2,6-di-tert-butyl) -4-Methylphenyl) pentaerythritol diphosphite, tetrakis (2,6-di-tert-butylphenyl) 4,4'-biphenylene phosphite and the like can be preferably used.

  Specific examples of thioether compounds include dilauryl thiodipropionate, ditridecyl thiodipropionate, dimyristyl thiodipropionate, distearyl thiodipropionate, pentaerythritol-tetrakis (3-lauryl thiopropionate), Pentaerythritol-tetrakis (3-dodecylthiopropionate), pentaerythritol-tetrakis (3-octadecylthiopropionate), pentaerythritol tetrakis (3-myristylthiopropionate), pentaerythritol-tetrakis (3-stearylthio) Propionate) and the like.

  Specific examples of the light stabilizer include benzophenone compounds, benzotriazole compounds, aromatic benzoate compounds, oxalic acid anilide compounds, cyanoacrylate compounds, hindered amine compounds, and the like.

  Examples of the benzophenone compounds include benzophenone, 2,4-dihydroxybenzophenone, 2,2′-dihydroxybenzophenone, 2,2 ′, 4,4′-tetrahydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2,2 ′. -Dihydroxy-4,4'-dimethoxybenzophenone, 2,2'-dihydroxy-4,4'-dimethoxy-5-sulfobenzophenone, 2-hydroxy-4-octoxybenzophenone, 2-hydroxy-4-dodecyloxybenzophenone 2-hydroxy-4-octoxybenzophenone, 2-hydroxy-4-methoxy-5-sulfobenzophenone, 5-chloro-2-hydroxybenzophenone, 2-hydroxy-4-octoxybenzophenone, 2-hydroxy-4-methoxy -2 - carboxy benzophenone, 2-hydroxy-4- (2-hydroxy-3-methyl - acryloxy-isopropoxyphenyl) benzophenone.

  Examples of the benzotriazole compound include 2- (5-methyl-2-hydroxyphenyl) benzotriazole, 2- (3,5-di-tert-butyl-2-hydroxyphenyl) benzotriazole, 2- (3,5- Di-tert-amyl-2-hydroxyphenyl) benzotriazole, 2- (3 ′, 5′-di-tert-butyl-4′-methyl-2′-hydroxyphenyl) benzotriazole, 2- (3,5- Di-tert-amyl-2-hydroxyphenyl) -5-chlorobenzotriazole, 2- (5-tert-butyl-2-hydroxyphenyl) benzotriazole, 2- [2′-hydroxy-3 ′, 5′-bis (Α, α-Dimethylbenzyl) phenyl] benzotriazole, 2- [2′-hydroxy-3 ′, 5′-bis (α, α Dimethylbenzyl) phenyl] -2H- benzotriazole, 2- (4'-octoxy-2'-hydroxyphenyl) benzotriazole.

  Examples of the aromatic benzoate compounds include alkylphenyl salicylates such as p-tert-butylphenyl salicylate and p-octylphenyl salicylate.

  Examples of oxalic acid anilide compounds include 2-ethoxy-2′-ethyloxalic acid bisanilide, 2-ethoxy-5-tert-butyl-2′-ethyloxalic acid bisanilide, and 2-ethoxy-3′-. Examples include dodecyl oxalic acid bisanilide.

  Examples of the cyanoacrylate compound include ethyl-2-cyano-3,3'-diphenyl acrylate, 2-ethylhexyl-cyano-3,3'-diphenyl acrylate, and the like.

  Examples of hindered amine compounds include 4-acetoxy-2,2,6,6-tetramethylpiperidine, 4-stearoyloxy-2,2,6,6-tetramethylpiperidine, 4-acryloyloxy-2,2,6, 6-tetramethylpiperidine, 4- (phenylacetoxy) -2,2,6,6-tetramethylpiperidine, 4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 4-methoxy-2,2, 6,6-tetramethylpiperidine, 4-octadecyloxy-2,2,6,6-tetramethylpiperidine, 4-cyclohexyloxy-2,2,6,6-tetramethylpiperidine, 4-benzyloxy-2,2 , 6,6-tetramethylpiperidine, 4-phenoxy-2,2,6,6-tetramethylpiperidine, 4- (ethylcarba Yloxy) -2,2,6,6-tetramethylpiperidine, 4- (cyclohexylcarbamoyloxy) -2,2,6,6-tetramethylpiperidine, 4- (phenylcarbamoyloxy) -2,2,6,6 -Tetramethylpiperidine, bis (2,2,6,6-tetramethyl-4-piperidyl) carbonate, bis (2,2,6,6-tetramethyl-4-piperidyl) oxalate, bis (2,2,6 , 6-tetramethyl-4-piperidyl) malonate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (2,2,6,6-tetramethylpi-4-peridyl) adipate, bis (2,2,6,6-tetramethylpi-4-peridyl) terephthalate, 1,2-bis (2,2,6,6-tetramethylpi-4-peridylo) Cis) -ethane, α, α′-bis (2,2,6,6-tetramethyl-4-piperidyloxy) -p-xylene, bis (2,2,6,6-tetramethyl-4-piperidyl) -Tolylene-2,4-dicarbamate, bis (2,2,6,6-tetramethyl-4-piperidyl) -hexamethylene-1,6-dicarbamate, tris (2,2,6,6-tetramethyl -4-piperidyl) -benzene-1,3,5-tricarboxylate, tris (2,2,6,6-tetramethyl-4-piperidyl) -benzene-1,3,4-tricarboxylate, 1- “2- {3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionyloxy} -2,2,6,6-tetramethylpiperidine, 1,2,3,4-butanetetracarboxylic acid And 1,2,2, , 6-Pentamethyl-4-piperidinol and β, β, β ′, β′-tetramethyl-3,9- [2,4,8,10-tetraoxaspiro (5,5) undecane] dimethanol And the like. In this invention, E component may be used by 1 type and may be used in combination of 2 or more type. As the stabilizer component, a hindered phenol compound and / or a benzotriazole compound are preferable. The content of the stabilizer is preferably 0.01 to 3 parts by weight, more preferably 0.03 to 2 parts by weight, per 100 parts by weight of the polylactic acid composition.

<Crystallization accelerator>
The polylactic acid composition of the present invention can contain an organic or inorganic crystallization accelerator. By containing the crystallization accelerator, the action of the phosphoric acid ester metal salt can be further enhanced, and a molded product having excellent mechanical properties, heat resistance, and moldability can be obtained.

  That is, by applying the crystallization accelerator, the moldability and crystallinity of the polylactic acid composition are improved, and a molded product that is sufficiently crystallized even in normal injection molding and excellent in heat resistance and moist heat resistance can be obtained. . In addition, the manufacturing time for manufacturing the molded product can be greatly shortened, and the economic effect is great.

  As the crystallization nucleating agent used in the present invention, those generally used as crystallization nucleating agents for crystalline resins can be used, and both inorganic crystallization nucleating agents and organic crystallization nucleating agents are used. be able to.

As inorganic crystallization nucleating agents, talc, kaolin, silica, synthetic mica, clay, zeolite, graphite, carbon black, zinc oxide, magnesium oxide, titanium oxide, calcium carbonate, calcium sulfate, barium sulfate, calcium sulfide, boron nitride , Montmorillonite, neodymium oxide, aluminum oxide, phenylphosphonate metal salt and the like.
These inorganic crystallization nucleating agents are treated with various dispersing aids in order to enhance the dispersibility in the composition and the effect thereof, and are in a highly dispersed state with a primary particle size of about 0.01 to 0.5 μm. Are preferred.

  Organic crystallization nucleating agents include calcium benzoate, sodium benzoate, lithium benzoate, potassium benzoate, magnesium benzoate, barium benzoate, calcium oxalate, disodium terephthalate, dilithium terephthalate, dipotassium terephthalate, Sodium laurate, potassium laurate, sodium myristate, potassium myristate, calcium myristate, barium myristate, sodium octacolate, calcium octacolate, sodium stearate, potassium stearate, lithium stearate, calcium stearate, magnesium stearate , Barium stearate, sodium montanate, calcium montanate, sodium toluate, sodium salicylate, potassium salicylate, salicy Organic carboxylic acid metal salts such as zinc acid, aluminum dibenzoate, β-naphthoic acid sodium, β-naphthoic acid potassium, sodium cyclohexanecarboxylic acid and the like, and organic sulfonic acid metal salts such as sodium p-toluenesulfonate and sodium sulfoisophthalate. Can be mentioned.

  Also, organic carboxylic acid amides such as stearic acid amide, ethylenebislauric acid amide, palmitic acid amide, hydroxystearic acid amide, erucic acid amide, trimesic acid tris (tert-butylamide), low density polyethylene, high density polyethylene, polyiso Propylene, polybutene, poly-4-methylpentene, poly-3-methylbutene-1, polyvinylcycloalkane, polyvinyltrialkylsilane, high melting point polylactic acid, sodium salt of ethylene-acrylic acid copolymer, sodium of styrene-maleic anhydride copolymer Examples thereof include salts (so-called ionomers), benzylidene sorbitol and derivatives thereof such as dibenzylidene sorbitol.

Among these, at least one selected from talc and organic carboxylic acid metal salts is preferably used. Only one type of crystallization nucleating agent may be used in the present invention, or two or more types may be used in combination.
The content of the crystallization accelerator is preferably 0.01 to 30 parts by weight, more preferably 0.05 to 20 parts by weight, per 100 parts by weight of the polylactic acid composition.

<Filler>
The polylactic acid composition of the present invention can contain an organic or inorganic filler. By containing the filler component, a molded product having excellent mechanical properties, heat resistance, and moldability can be obtained.

  Organic fillers such as rice husks, wood chips, okara, waste paper ground materials, clothing ground materials, cotton fibers, hemp fibers, bamboo fibers, wood fibers, kenaf fibers, jute fibers, banana fibers, coconut fibers Plant fibers such as pulp or cellulose fibers processed from these plant fibers and fibrous fibers such as animal fibers such as silk, wool, angora, cashmere and camel, synthetic fibers such as polyester fibers, nylon fibers and acrylic fibers , Paper powder, wood powder, cellulose powder, rice husk powder, fruit husk powder, chitin powder, chitosan powder, protein, starch and the like. From the viewpoint of moldability, powdery materials such as paper powder, wood powder, bamboo powder, cellulose powder, kenaf powder, rice husk powder, fruit husk powder, chitin powder, chitosan powder, protein powder, and starch are preferred. Powder, bamboo powder, cellulose powder and kenaf powder are preferred. Paper powder and wood powder are more preferable. Paper dust is particularly preferable.

These organic fillers may be those directly collected from natural products, but may also be those obtained by recycling waste materials such as waste paper, waste wood and old clothes.
The wood is preferably a softwood material such as pine, cedar, oak or fir, or a hardwood material such as beech, shii or eucalyptus.

  Paper powder is an adhesive from the viewpoint of moldability, especially emulsion-based adhesives such as vinyl acetate resin-based emulsions and acrylic resin-based emulsions when processing paper, polyvinyl alcohol-based adhesives, polyamide-based adhesives, etc. Preferred examples include those containing a hot melt adhesive.

  In the present invention, the amount of the organic filler is not particularly limited, but from the viewpoint of moldability and heat resistance, it is preferably 1 to 300 parts by weight, more preferably 5 to 200 parts by weight per 100 parts by weight of polylactic acid. Parts, more preferably 10 to 150 parts by weight, particularly preferably 15 to 100 parts by weight. If the blending amount of the organic filler is less than 1 part by weight, the effect of improving the moldability of the composition is small, and if it exceeds 300 parts by weight, uniform dispersion of the filler becomes difficult, or other than moldability and heat resistance In addition, the strength and appearance of the material may decrease, which is not preferable.

  The polylactic acid composition of the present invention can contain an inorganic filler. A composition excellent in mechanical properties, heat resistance and moldability can be obtained by the inorganic filler. As the inorganic filler used in the present invention, a fibrous, plate-like, or powder-like material used for reinforcing ordinary thermoplastic resins can be used.

  Specifically, for example, carbon nanotube, glass fiber, asbestos fiber, carbon fiber, graphite fiber, metal fiber, potassium titanate whisker, aluminum borate whisker, magnesium whisker, silicon whisker, wollastonite, imogolite, sepiolite, Asbestos, slag fiber, zonolite, gypsum fiber, silica fiber, silica. Fibrous inorganic fillers such as alumina fiber, zirconia fiber, boron nitride fiber, silicon nitride fiber and boron fiber, layered silicate, layered silicate exchanged with organic onium ions, glass flake, non-swellable mica, graphite, metal Foil, ceramic beads, talc, clay, mica, sericite, zeolite, bentonite, dolomite, kaolin, powdered silicic acid, feldspar powder, potassium titanate, shirasu balloon, calcium carbonate, magnesium carbonate, barium sulfate, calcium oxide, aluminum oxide, Examples thereof include plate-like and particulate inorganic fillers such as carbon nanoparticles such as titanium oxide, aluminum silicate, silicon oxide, gypsum, novaculite, dawsonite, and white clay fullerene.

  Specific examples of layered silicates include smectite clay minerals such as montmorillonite, beidellite, nontronite, saponite, hectorite, and soconite, various clay minerals such as vermiculite, halosite, kanemite, and kenyanite, Li-type fluorine teniolite, Na And swellable mica such as Li-type fluorine teniolite, Li-type tetrasilicon fluorine mica and Na-type tetrasilicon fluorine mica. These may be natural or synthetic. Among these, smectite clay minerals such as montmorillonite and hectorite, and swellable synthetic mica such as Li type fluorine teniolite and Na type tetrasilicon fluorine mica are preferable.

  Among these inorganic fillers, fibrous or plate-like inorganic fillers are preferable, and glass fiber, wollastonite, aluminum borate whisker, potassium titanate whisker, mica, and kaolin, a cation-exchanged layered silicate. Is preferred. The aspect ratio of the fibrous filler is preferably 5 or more, more preferably 10 or more, and further preferably 20 or more.

Such a filler may be coated or converged with a thermoplastic resin such as an ethylene / vinyl acetate copolymer or a thermosetting resin such as an epoxy resin, or may be treated with a coupling agent such as aminosilane or epoxysilane. May be.
The amount of the inorganic filler is preferably 0.1 to 200 parts by weight, more preferably 0.5 to 100 parts by weight, still more preferably 1 to 50 parts by weight, particularly preferably 100 parts by weight of the polylactic acid composition. Is 1 to 30 parts by weight, most preferably 1 to 20 parts by weight.

<Release agent>
The polylactic acid composition of the present invention can contain a release agent. As the mold release agent used in the present invention, those used for ordinary thermoplastic resins can be used.
Specific examples of release agents include fatty acids, fatty acid metal salts, oxy fatty acids, paraffins, low molecular weight polyolefins, fatty acid amides, alkylene bis fatty acid amides, aliphatic ketones, fatty acid partial saponified esters, fatty acid lower alcohol esters, fatty acid polyvalents. Examples include alcohol esters, fatty acid polyglycol esters, and modified silicones. By blending these, a polylactic acid molded product excellent in mechanical properties, moldability, and heat resistance can be obtained.

  Fatty acids having 6 to 40 carbon atoms are preferred. Specifically, oleic acid, stearic acid, lauric acid, hydroxystearic acid, behenic acid, arachidonic acid, linoleic acid, linolenic acid, ricinoleic acid, palmitic acid, montan Examples thereof include acids and mixtures thereof. The fatty acid metal salt is preferably an alkali (earth) metal salt of a fatty acid having 6 to 40 carbon atoms, and specific examples include calcium stearate, sodium montanate, and calcium montanate.

  Examples of the oxy fatty acid include 1,2-oxysteric acid. Paraffin having 18 or more carbon atoms is preferable, and examples thereof include liquid paraffin, natural paraffin, microcrystalline wax, petrolactam and the like.

  As the low molecular weight polyolefin, for example, those having a molecular weight of 5000 or less are preferable, and specific examples include polyethylene wax, maleic acid-modified polyethylene wax, oxidized type polyethylene wax, chlorinated polyethylene wax, and polypropylene wax. Fatty acid amides having 6 or more carbon atoms are preferred, and specific examples include oleic acid amide, erucic acid amide, and behenic acid amide.

  The alkylene bis fatty acid amide is preferably one having 6 or more carbon atoms, and specifically includes methylene bis stearic acid amide, ethylene bis stearic acid amide, N, N-bis (2-hydroxyethyl) stearic acid amide and the like. As the aliphatic ketone, those having 6 or more carbon atoms are preferable, and examples thereof include higher aliphatic ketones.

  Examples of the fatty acid partial saponified ester include a montanic acid partial saponified ester. Examples of the fatty acid lower alcohol ester include stearic acid ester, oleic acid ester, linoleic acid ester, linolenic acid ester, adipic acid ester, behenic acid ester, arachidonic acid ester, montanic acid ester, isostearic acid ester and the like.

  Examples of fatty acid polyhydric alcohol esters include glycerol tristearate, glycerol distearate, glycerol monostearate, pentaerythritol tetrastearate, pentaerythritol tristearate, pentaerythritol dimyristate, pentaerythritol Examples include tall stearate, pentaerythritol adipate stearate, and sorbitan monobehenate. Examples of fatty acid polyglycol esters include polyethylene glycol fatty acid esters and polypropylene glycol fatty acid esters.

  Examples of the modified silicone include polyether-modified silicone, higher fatty acid alkoxy-modified silicone, higher fatty acid-containing silicone, higher fatty acid ester-modified silicone, methacryl-modified silicone, and fluorine-modified silicone.

  Of these, fatty acid, fatty acid metal salt, oxy fatty acid, fatty acid ester, fatty acid partial saponified ester, paraffin, low molecular weight polyolefin, fatty acid amide, and alkylene bis fatty acid amide are preferred, and fatty acid partial saponified ester and alkylene bis fatty acid amide are more preferred. Of these, montanic acid ester, montanic acid partial saponified ester, polyethylene wax, acid value polyethylene wax, sorbitan fatty acid ester, erucic acid amide, and ethylene bisstearic acid amide are preferred, and particularly, montanic acid partial saponified ester and ethylene bisstearic acid amide are preferred. preferable.

  A mold release agent may be used by 1 type and may be used in combination of 2 or more type. The content of the release agent is preferably 0.01 to 3 parts by weight, more preferably 0.03 to 2 parts by weight, with respect to 100 parts by weight of polylactic acid.

<Antistatic agent>
The polylactic acid composition of the present invention may contain an antistatic agent, specifically, a quaternary ammonium salt compound such as (β-lauramidopropionyl) trimethylammonium sulfate, sodium dodecylbenzenesulfonate, Examples thereof include sulfonate compounds and alkyl phosphate compounds.
One antistatic agent may be used, or two or more antistatic agents may be used in combination. When the antistatic agent is contained, the amount is preferably 0.05 to 5 parts by weight, more preferably 0.1 to 5 parts by weight with respect to 100 parts by weight of the polylactic acid composition.

<Plasticizer>
The polylactic acid composition of the present invention can contain a plasticizer, and generally known plasticizers can be used as the plasticizer to be used. For example, a polyester plasticizer, a glycerin plasticizer, a polyvalent carboxylic ester plasticizer, a phosphoric ester plasticizer, a polyalkylene glycol plasticizer, and an epoxy plasticizer.

  As a polyester plasticizer, acid components such as adipic acid, sebacic acid, terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid, diphenyldicarboxylic acid and ethylene glycol, propylene glycol, 1,3-butanediol, 1,4-butanediol, Examples thereof include polyesters composed of diol components such as 1,6-hexanediol and diethylene glycol, and polyesters composed of hydroxycarboxylic acids such as polycaprolactone. These polyesters may be end-capped with a monofunctional carboxylic acid or a monofunctional alcohol.

  Examples of the glycerol plasticizer include glycerol monostearate, glycerol distearate, glycerol monoacetomonolaurate, glycerol monoacetomonostearate, glycerol diacetomonooleate, and glycerol monoacetomonomontanate.

  Polyvalent carboxylic acid plasticizers include dimethyl phthalate, diethyl phthalate, dibutyl phthalate, diheptyl phthalate, dibenzyl phthalate, butyl benzyl phthalate, trimellitic acid tributyl, trimellitic acid trioctyl, Trimellitic acid esters such as trihexyl meritate, isodecyl adipate, adipic acid esters such as adipate-n-decyl-n-octyl, citrate esters such as tributyl acetylcitrate, and bis (2-ethylhexyl) azelate Examples include sebacic acid esters such as azelaic acid ester, dibutyl sebacate, and bis (2-ethylhexyl) sebacate.

  Examples of the phosphate ester plasticizer include tributyl phosphate, tris phosphate (2-ethylhexyl), trioctyl phosphate, triphenyl phosphate, tricresyl phosphate, diphenyl-2-ethylhexyl phosphate, and the like.

  Polyalkylene glycol plasticizers such as polyethylene glycol, polypropylene glycol, polytetramethylene glycol, poly (ethylene oxide.propylene oxide) block and / or random copolymers, ethylene oxide addition polymers of bisphenols, tetrahydrofuran addition polymers of bisphenols, etc. And end-capping compounds such as a terminal epoxy-modified compound, a terminal ester-modified compound, and a terminal ether-modified compound.

  Examples of the epoxy plasticizer include an epoxy triglyceride composed of alkyl epoxy stearate and soybean oil, and an epoxy resin using bisphenol A and epichlorohydrin as raw materials.

  Specific examples of other plasticizers include benzoic acid esters of aliphatic polyols such as neopentyl glycol dibenzoate, diethylene glycol dibenzoate, triethylene glycol-bis (2-ethylbutyrate), and fatty acids such as stearamide. Examples thereof include fatty acid esters such as amide and butyl oleate, oxyacid esters such as methyl acetylricinoleate and butyl acetylricinoleate, pentaerythritol, various sorbitols, polyacrylic acid esters, silicone oils, and paraffins.

  As the plasticizer, at least one selected from polyester-type plasticizers and polyalkylene-type plasticizers can be preferably used, and only one type may be used, or two or more types may be used in combination.

  The amount when the plasticizer is contained is preferably 0.01 to 30 parts by weight, more preferably 0.05 to 20 parts by weight, still more preferably 0.1 to 10 parts by weight per 100 parts by weight of the polylactic acid composition. It is. In the present invention, the crystallization nucleating agent and the plasticizer may be used singly or in combination.

<Impact resistance improver>
The impact resistance improver that may be added to the polylactic acid composition of the present invention can be used for improving the impact resistance of a thermoplastic resin, and is not particularly limited. For example, at least one selected from the following impact resistance improvers can be used.

  Specific examples of impact modifiers include ethylene-propylene copolymers, ethylene-propylene-nonconjugated diene copolymers, ethylene-butene-1 copolymers, various acrylic rubbers, ethylene-acrylic acid copolymers and their Alkali metal salt (so-called ionomer) ethylene-glycidyl (meth) acrylate copolymer, ethylene-acrylate copolymer (for example, ethylene-ethyl acrylate copolymer, ethylene-butyl acrylate copolymer), modified ethylene- Propylene copolymer, diene rubber (eg, polybutadiene, polyisoprene, polychloroprene), diene and vinyl copolymer (eg, styrene-butadiene random copolymer, styrene-butadiene block copolymer, styrene-butadiene-styrene block copolymer) , Styrene-a A random copolymer, styrene-isoprene block copolymer, styrene-isoprene-styrene block copolymer, polybutadiene grafted with styrene, butadiene-acrylonitrile copolymer), polyisobutylene, isobutylene and butadiene or Examples include copolymers with isoprene, natural rubber, thiocol rubber, polysulfide rubber, polyurethane rubber, polyether rubber, epichlorohydrin rubber, and the like.

  In addition, those having various cross-linking degrees, various micro structures such as those having a cis structure, a trans structure, etc., a core layer and one or more shell layers covering the core layer, and adjacent layers are composed of heterogeneous polymers. A so-called core-shell type multi-layered polymer can also be used.

Further, the various (co) polymers mentioned in the above specific examples may be any of randomand copolymers, block copolymers, block copolymers and the like, and can be used as the impact resistance improver of the present invention.
The impact resistance improver is preferably 1 to 30 parts by weight, more preferably 5 to 20 parts by weight, and still more preferably 10 to 20 parts by weight with respect to 100 parts by weight of polylactic acid.

<Others>
Moreover, in this invention, you may contain thermosetting resins, such as a phenol resin, a melamine resin, a thermosetting polyester resin, a silicone resin, an epoxy resin, in the range which is not contrary to the meaning of this invention.
In the present invention, flame retardants such as bromine, phosphorus, silicone, and antimony compounds may be included within the scope not departing from the spirit of the present invention.

  Colorants containing organic and inorganic dyes and pigments, for example, oxides such as titanium dioxide, hydroxides such as alumina white, sulfides such as zinc sulfide, ferrocyanides such as bitumen, and chromium such as zinc chromate Contains acid salts, sulfates such as barium sulfate, carbonates such as calcium carbonate, silicates such as ultramarine, phosphates such as manganese violet, carbon such as carbon black, metal colorants such as bronze powder and aluminum powder, etc. You may let them.

  Also, nitroso type such as naphthol green B, nitro type such as naphthol yellow S, azo type such as naphthol red, chromophthal yellow, phthalocyanine type such as phthalocyanine blue and fast sky blue, condensed polycyclic colorants such as indanthrone blue In addition, additives such as slidability improvers such as graphite and fluorine resin may be added. These additives can be used alone or in combination of two or more.

  A polylactic acid composition containing these additives can be prepared by mixing each component. For the mixing, a tumbler, a V-type blender, a super mixer, a nauter mixer, a Banbury mixer, a kneading roll, a monoaxial or biaxial extruder can be used. The resulting composition can be molded as it is or after being once pelletized with a melt extruder.

  The shape of the pellet may be any shape such as a spherical shape, a die shape, a linear shape, a curved shape, and a cross-sectional shape such as a round shape, an oval shape, a flat shape, a triangular shape, a polygon shape having a square shape or more, and a star shape. However, it is preferable to have a shape suitable for further molding the pellets by various molding methods. Specifically, the pellet length is preferably 1 to 7 mm, the major axis 3 to 5 mm, and the minor axis 1 to 4 mm. Further, it is preferable that the shape does not vary.

<Manufacture of molded products>
Molded products made of the polylactic acid composition of the present invention are injection molded products, extruded molded products, vacuum molded products, compressed air molded products, blow molded products, and the like, specifically, pellets, fibers and cloth, and other materials. And the like, including a fiber structure, a film, a sheet, a sheet nonwoven fabric, and a compression molded product.

  The polylactic acid composition of the present invention is not limited in its melt molding method, and those produced by a known pellet production method can be preferably used. That is, after the polylactic acid composition applied in the form of a strand or plate is completely solidified or is not completely solidified and is still in a molten state, a method such as cutting in air or water Are conventionally known, but any of them can be suitably applied to the polylactic acid composition of the present invention.

  Conventionally known molding methods can be applied to the injection molded product of the present invention without any limitation. From the viewpoint of increasing the crystallization of the molded product and the molding cycle at the time of injection molding, the mold temperature is preferably 30 ° C. or more, more preferably Is 60 ° C. or higher, more preferably 70 ° C. or higher. However, in order to prevent deformation of the molded product, the mold temperature is preferably 140 ° C. or lower, more preferably 120 ° C. or lower, and further preferably 110 ° C. or lower.

  Examples of these molded products include various housings, electric / electronic parts such as gears and gears, building members, civil engineering members, agricultural materials, automobile parts (interior parts, exterior parts, etc.), and daily parts.

<Fiber and fiber structure>
For the fiber and fiber structure comprising the polylactic acid composition of the present invention, materials obtained by ordinary melt spinning and subsequent post-processing steps can be suitably used.
That is, after the polylactic acid composition is melted by an extruder type or pressure melter type melt extruder, it is weighed by a gear pump, filtered in a pack, and then monofilament and multifilament from a nozzle provided on the base. Etc.
The shape of the base and the number of the bases are not particularly limited, and any of circular, irregular, solid, hollow and the like can be adopted. The discharged yarn is immediately cooled and solidified, then converged, added with oil, and wound. The winding speed is not particularly limited, but is preferably in a range of 300 m / min to 5000 m / min because a stereo complex crystal is easily formed.

  From the viewpoint of stretchability, a winding speed at which the stereocomplex crystallization ratio of the undrawn yarn is 0% is preferable. The undrawn yarn that has been wound is then subjected to a drawing step, but the spinning step and the drawing step do not necessarily need to be separated, and even if a direct spinning drawing method is used in which the drawing is continued without being wound once after spinning. I do not care.

  The stretching may be one-stage stretching or multi-stage stretching of two or more stages. From the viewpoint of producing a high-strength fiber, the stretching ratio is preferably 3 times or more, and more preferably 4 times or more. Preferably 3 to 10 times is selected. However, if the draw ratio is too high, the fiber is devitrified and whitened, the strength of the fiber is lowered, the elongation at break is too low, and it is not preferable for fiber use.

As a preheating method for stretching, in addition to the temperature rise of the roll, a flat or pin-like contact heater, a non-contact hot plate, a heat medium bath, and the like can be used, and a commonly used method may be used.
Following the stretching, it is preferable that the heat treatment is performed at a temperature of 170 ° C. or higher and lower than the melting point of the polylactic acid composition before winding. In addition to the hot roller, any method such as a contact heater or a non-contact hot plate can be adopted for the heat treatment. The stretching temperature is selected from the glass transition point of polylactic acid to 170 ° C., preferably 70 ° C. to 140 ° C., particularly preferably 80 ° C. to 130 ° C.

  After stretching, heat-fixing at 170 ° C. to 220 ° C. under tension to obtain a fiber composed of a polylactic acid composition having a high stereocomplex crystallization rate, low heat shrinkage, and a strength of 3.5 cN / dTex or more. Can do.

The fiber of the present invention having high strength and excellent heat resistance and heat and heat resistance stability can take the form of various fiber structures such as woven fabrics, knitted fabrics, nonwoven fabrics, and molded articles such as cups.
Specifically, thread form products such as sewing thread, embroidery thread, string, fabric such as woven fabric, knitted fabric, nonwoven fabric, felt, outer clothing such as shirt, blouson, pants, coat, sweater, uniform, underwear, pantyhose, socks, Lining, interlining, sports clothing, high value-added clothing products such as women's clothing and formal wear, clothing products such as cups and pads, curtains, carpets, chair upholstery, mats, furniture, baskets, furniture upholstery, wall materials, etc. Products for daily use such as belts and slings, as well as various textile products such as canvas, belts, nets, ropes, heavy cloth, bags, industrial materials such as felts and filters, vehicle interior products, and artificial leather products.

  The fiber and fiber structure of the present invention may be composed of a single fiber formed from a polylactic acid composition, or may be mixed with other types of fibers. In addition to various combinations with fiber structures composed of other types of fibers, mixed modes include mixed yarns with other fibers, composite false twisted yarns, mixed spun yarns, long and short composite yarns, fluid processed yarns, covering yarns, and twisted yarns. Examples thereof include union, union, pile, pile, mixed cotton, mixed non-woven fabric of long fibers and short fibers, and felt. When mixed, in order to exhibit the characteristics of the polylactic acid composition, the mixed ratio is selected in the range of 1 wt% or more, more preferably 10 wt% or more, and further preferably 30 wt% or more.

  Other fibers to be mixed, for example, cellulose fibers such as cotton, hemp, rayon and tencel, wool, silk, acetate, polyester, nylon, acrylic, vinylon, polyolefin, polyurethane and the like can be raised.

<Film, sheet>
Moreover, the film and sheet | seat which consist of the polylactic acid composition of this invention are shape | molded by the conventionally well-known method.
For example, in a film or sheet, a molding technique such as extrusion molding or cast molding can be used. That is, an unstretched film can be extruded using an extruder or the like equipped with a T die, a circular die, or the like, and further stretched and heat treated to be molded. At this time, the unstretched film can be used as it is as a sheet.
In the case of forming a film, if a material obtained by melt-kneading the polylactic acid composition and the above-described various components in advance can be used, it can be formed through melt-kneading at the time of extrusion molding.

When extruding an unstretched film, an unstretched film with few surface defects can be obtained by blending a molten resin with an electrostatic adhesive such as a sulfonic acid quaternary phosphonium salt.
Moreover, an unstretched film can also be cast-molded by melt | dissolving, casting, and drying and solidifying a polylactic acid composition and an additive component using solvents, such as chloroform and a methylene dichloride, for example.

Unstretched film can be uniaxially stretched longitudinally in the direction of mechanical flow and transversely uniaxially stretched in the direction perpendicular to the direction of mechanical flow. Simultaneous biaxial stretching by roll and tenter stretching, and simultaneous biaxial stretching by tenter stretching A biaxially stretched film can be produced by stretching by a biaxial stretching method using a method such as tubular stretching. Further, the film is usually subjected to a heat setting treatment after stretching in order to suppress heat shrinkability and the like.
The stretched film thus obtained can be subjected to surface activation treatment such as plasma treatment, amine treatment, and corona treatment by a conventionally known method if desired.

  The film and sheet of the present invention can be used in combination with other types of films and sheets other than a single form. Examples of mixed use include various combinations with films and sheets made of other types of materials, such as lamination and lamination, and combinations with other types of forms such as injection molded articles and fiber structures.

  The present invention will be described more specifically with reference to the following examples. However, the present invention is not limited to these examples.

In addition, each value in a present Example was calculated | required according to the following method.
1. Measuring method (1) Weight average molecular weight and number average molecular weight (Mn) of polymer:
The weight average molecular weight and number average molecular weight (Mn) of the polymer were converted to standard polystyrene by gel permeation chromatography (GPC).
The GPC measuring instrument used was a detector, a differential refractometer, and chloroform as the eluent, flowed at a temperature of 40 ° C. and a flow rate of 1.0 ml / min, and 10 μl of a sample having a concentration of 1 mg / ml (chloroform) was injected and measured.

(2) Measurement of crystal melting point and melting enthalpy:
Measurement was performed using a differential scanning calorimeter (DSC) manufactured by TA Instruments.
A sample of 5 mg was heated from room temperature to 200 ° C. at a temperature rising rate of 20 ° C./min in a nitrogen atmosphere, and a crystal melting temperature (Tmh) and a crystal melting heat (ΔHmh) were determined.

[Production Example 1] Production of cyclic carbodiimide compound CC1 (MW = 194):
ω- laurolactam (0.05 mol) and trimethyl oxonium tetrafluoroborate (0.1 mol), was charged under _{N 2} into the reactor which was placed a stirrer and a heating device of dichloromethane 100 ml, subjected to an atmosphere of _{N 2} at reflux the reaction It was. After 6 hours of reaction, the generated salt was removed by filtration, and the filtrate was washed three times with 100 ml of a 15% aqueous potassium carbonate solution and further washed three times with 100 ml of distilled water. The organic layer was dehydrated with 5 g of sodium sulfate, and dichloromethane was removed under reduced pressure to obtain an intermediate product A.

Next, intermediate product A (0.1 mol), hydroxylamine hydrochloride (0.11 mol), sodium bicarbonate (0.15 mol), and 100 ml of methanol were placed in a reactor equipped with a stirrer and a heating device under N ₂ atmosphere. The reaction was refluxed under N ₂ atmosphere. After 6 hours of reaction, the reaction mixture was filtered, and intermediate product B was obtained by recrystallization from the filtrate.

Next, an intermediate product B (0.1 mol) and 50 ml of pyridine are charged and stirred in a reactor equipped with a stirrer, a dropping funnel and an ice bath in an N ₂ atmosphere. Methanesulfonyl chloride (0.11 mol) is gradually added dropwise thereto. After the dropwise addition, the mixture is reacted for 6 hours in an ice bath under N ₂ atmosphere. After the reaction, when transferred to a beaker containing 500 ml of water, a pale yellow solid is precipitated. The solid was collected by filtration and washed several times with 100 ml of water to obtain intermediate product C.

Next, an intermediate product C (0.1 mol) and 50 ml of dimethoxyethane were charged into a reactor equipped with a stirrer and an ice bath, and potassium tert-butoxide (0.11 mol) was dispersed therein under an N ₂ atmosphere. 20 ml of dimethoxyethane was gradually added. After reacting in an ice bath for 2 hours, CC1 having the following structure was obtained from the reaction solution. The structure of CC1 was confirmed by NMR and IR.

[Production Example 2] Production of cyclic carbodiimide compound CC2 (MW = 252):
o-Nitrophenol (0.11 mol), 1,2-dibromoethane (0.05 mol), potassium carbonate (0.33 mol), 200 ml of N, N-dimethylformamide were added to a reactor equipped with a stirrer and a heating device. _After charging under _two atmospheres and reacting at 130 ° C. for 12 hours, DMF was removed under reduced pressure, and the resulting solid was dissolved in 200 ml of dichloromethane and separated three times with 100 ml of water. The organic layer was dehydrated with 5 g of sodium sulfate, and dichloromethane was removed under reduced pressure to obtain an intermediate product D (nitro form).

  Next, intermediate product D (0.1 mol), 5% palladium carbon (Pd / C) (1 g), and 200 ml of ethanol / dichloromethane (70/30) were charged into a reactor equipped with a stirrer, and 5 hydrogen substitution was performed. The reaction is performed in a state where hydrogen is constantly supplied at 25 ° C., and the reaction is terminated when there is no decrease in hydrogen. When Pd / C was recovered and the mixed solvent was removed, an intermediate product E (amine body) was obtained.

Next, in a reactor equipped with a stirrer, a heating device, and a dropping funnel, triphenylphosphine dibromide (0.11 mol) and 150 ml of 1,2-dichloroethane are charged and stirred in an N ₂ atmosphere. A solution prepared by dissolving intermediate product E (0.05 mol) and triethylamine (0.25 mol) in 50 ml of 1,2-dichloroethane is gradually added dropwise thereto at 25 ° C. After completion of dropping, the reaction is carried out at 70 ° C. for 5 hours. Thereafter, the reaction solution was filtered, and the filtrate was separated 5 times with 100 ml of water. The organic layer was dehydrated with 5 g of sodium sulfate, and 1,2-dichloroethane was removed under reduced pressure to obtain an intermediate product F (triphenylphosphine compound).

Next, in a reactor equipped with a stirrer and a dropping funnel, di-tert-butyl dicarbonate (0.11 mol), N, N-dimethyl-4-aminopyridine (0.055 mol), dichloromethane under N ₂ atmosphere. 150 ml is charged and stirred. Thereto, 100 ml of dichloromethane in which the intermediate product F (0.05 mol) is dissolved is slowly dropped at 25 ° C.
After dropping, react for 12 hours. Then, CC2 of the following structure was obtained by refine | purifying the solid substance obtained by removing dichloromethane. The structure of CC2 was confirmed by NMR and IR.

[Production Example 3] Production of cyclic carbodiimide compound CC3 (MW = 516) o-nitrophenol (0.11 mol), pentaerythrityl tetrabromide (0.025 mol), potassium carbonate (0.33 mol), N, N- 200 ml of dimethylformamide was charged in a reactor equipped with a stirrer and a heating device under N ₂ atmosphere, reacted at 130 ° C. for 12 hours, DMF was removed under reduced pressure, and the resulting solid was dissolved in 200 ml of dichloromethane, and 100 ml of water was used. Liquid separation was performed 3 times. The organic layer was dehydrated with 5 g of sodium sulfate, and dichloromethane was removed under reduced pressure to obtain an intermediate product D (nitro form).

  Next, intermediate product D (0.1 mol), 5% palladium carbon (Pd / C) (2 g), and 400 ml of ethanol / dichloromethane (70/30) were charged into a reactor equipped with a stirrer, and 5 hydrogen substitution was performed. The reaction was performed in a state where hydrogen was constantly supplied at 25 ° C., and the reaction was terminated when there was no decrease in hydrogen. When Pd / C was recovered and the mixed solvent was removed, an intermediate product E (amine body) was obtained.

Next, in a reactor equipped with a stirrer, a heating device, and a dropping funnel, triphenylphosphine dibromide (0.11 mol) and 150 ml of 1,2-dichloroethane are charged and stirred in an N ₂ atmosphere. A solution prepared by dissolving the intermediate product E (0.025 mol) and triethylamine (0.25 mol) in 50 ml of 1,2-dichloroethane is gradually added dropwise thereto at 25 ° C. After completion of dropping, the reaction is carried out at 70 ° C. for 5 hours. Thereafter, the reaction solution was filtered, and the filtrate was separated 5 times with 100 ml of water. The organic layer was dehydrated with 5 g of sodium sulfate, and 1,2-dichloroethane was removed under reduced pressure to obtain an intermediate product F (triphenylphosphine compound).

Next, in a reactor equipped with a stirrer and a dropping funnel, di-tert-butyl dicarbonate (0.11 mol), N, N-dimethyl-4-aminopyridine (0.055 mol), dichloromethane under N ₂ atmosphere. 150 ml is charged and stirred. Thereto, 100 ml of dichloromethane in which the intermediate product F (0.025 mol) is dissolved is slowly dropped at 25 ° C.
After dropping, react for 12 hours. Then, CC3 of the following structure was obtained by refine | purifying the solid substance obtained by removing dichloromethane. The structure of CC3 was confirmed by NMR and IR.

[Production Example 4]
As a raw material for the α-hydroxycarboxylic acid (B) component other than lactic acid, a cyclic dimer composed of 2-hydroxybutyric acid, a cyclic dimer composed of lactic acid and 2-hydroxybutyric acid, and a raw material for the lactic acid (A) component L-lactide was mixed in a molten state and adjusted so that 2-hydroxybutyric acid was 0.1 parts by weight with respect to 100 parts by weight of lactic acid (the optical purity of lactic acid was 99.9%). 2 parts by weight, 0.005 part by weight of tin octylate was added, and the reaction was carried out at 180 ° C. for 2 hours in a reactor equipped with a stirring blade in a nitrogen atmosphere. As a catalyst deactivator for tin octylate, 5 times An equivalent amount of DHPA was added, and then the remaining lactide at 13.3 Pa was removed and chipped to obtain a polylactic acid composition. The resulting polylactic acid composition had a carboxyl end group concentration of 14 equivalents / ton, a weight average molecular weight of 160,000, and a melting point of 175 ° C.

[Production Example 5]
As a raw material for the α-hydroxycarboxylic acid (B) component other than lactic acid, a cyclic dimer composed of 2-hydroxybutyric acid, a cyclic dimer composed of lactic acid and 2-hydroxybutyric acid, and a raw material for the lactic acid (A) component L-lactide was mixed in a molten state and adjusted so that 2-hydroxybutyric acid was 0.1 parts by weight with respect to 100 parts by weight of lactic acid (the optical purity of lactic acid was 99.9%). 2 parts by weight, 0.005 part by weight of tin octylate was added, and the reaction was carried out at 180 ° C. for 2 hours in a reactor equipped with a stirring blade in a nitrogen atmosphere. As a catalyst deactivator for tin octylate, 5 times An equivalent amount of DHPA was added, and then the remaining lactide at 13.3 Pa was removed and chipped to obtain a polylactic acid composition. The resulting polylactic acid composition had a carboxyl end group concentration of 16 equivalents / ton, a weight average molecular weight of 170,000, and a melting point of 174 ° C.

[Production Example 6]
50 parts by weight of the polylactic acid composition obtained by the operation of Production Example 4 and the polylactic acid composition obtained by the operation of Production Example 5 were each mixed with a phosphate metal salt (“ADEKA STAB” NA-11 manufactured by ADEKA Corporation). ) After mixing 0.3 parts by weight with a blender and vacuum drying at 110 ° C. for 5 hours, from the first supply port of the extruder, melt and knead while evacuating at a cylinder temperature of 270 ° C. and a vent pressure of 13.3 Pa. The strand was extruded into a chip with a chip cutter, and stereocomplex polylactic acid having a stereocomplex crystallinity (S) of 100% and a crystal melting temperature of 216 ° C. was obtained. The resulting stereocomplex polylactic acid had a carboxyl end group concentration of 11 equivalents / ton and a weight average molecular weight of 130,000.

[Production Example 7]
Glycolic acid, 2-hydroxybutyric acid, 2-hydroxyvaleric acid, 2-hydroxy-4-methyl-valeric acid, which are α-hydroxycarboxylic acids as raw materials for the α-hydroxycarboxylic acid (B) component other than lactic acid, are In a ratio of 7/4/1, a cyclic dimer composed of each, a cyclic dimer composed of lactic acid and 2-hydroxycarboxylic acid, and L-lactide as a raw material for the lactic acid (A) component were mixed in a molten state. , 100 parts by weight of lactic acid (the optical purity of lactic acid is 98.5%), adjusted so that 2-hydroxycarboxylic acid is 0.6 parts by weight, 0.2 parts by weight of molecular weight regulator, tin octylate Add 0.005 parts by weight, react in a reactor equipped with a stirring blade under nitrogen atmosphere at 180 ° C. for 2 hours, add 5 times equivalent of DHPA as a catalyst deactivator to tin octylate, 13.3 Pa remaining The existing lactide was removed and chipped to obtain a polylactic acid composition. The resulting polylactic acid composition had a carboxyl end group concentration of 14 equivalents / ton, a weight average molecular weight of 200,000, a melting point of 159 ° C., and a glass transition point of 63 ° C.

[Production Example 8]
50 parts by weight of each of the polylactic acid composition obtained by the operation of Production Example 7 and the polylactic acid composition obtained by the operation of Production Example 5, phosphate metal salt (“ADEKA STAB” NA-produced by ADEKA Corporation) 11) After mixing 0.3 parts by weight with a blender, vacuum drying at 110 ° C. for 5 hours, from the first supply port of the extruder, melt kneading while evacuating at a cylinder temperature of 270 ° C. and a vent pressure of 13.3 Pa, The strand was extruded into a water bath and chipped with a chip cutter to obtain stereocomplex polylactic acid having a stereocomplex crystallinity (S) of 100% and a crystal melting temperature of 216 ° C. The resulting stereocomplex polylactic acid had a carboxyl end group concentration of 11 equivalents / ton and a weight average molecular weight of 130,000.

[Example 1]
A twin-screw extruder (KTX46, L / D = 58. Manufactured by Kobe Steel, Ltd.) in which the set temperatures of the barrels 0 to 15 in order from the first supply port to the discharge unit were 180 ° C. to 210 ° C., respectively. In 8), the polylactic acid composition produced in Production Example 4 is quantitatively supplied from the first supply port, and the polylactic acid composition is produced from the second supply port provided with cyclic carbodiimide (CC2) at the barrel 14 position by the side feeder. When the product was 100 parts by weight, 1 part by weight of cyclic carbodiimide (CC2) was supplied, kneaded and pelletized to obtain a polylactic acid composition of the present invention containing a cyclic carbodiimide compound.
The carboxyl end group concentration of the obtained polylactic acid composition was reduced to 0.4 equivalent / ton or less. The resulting polylactic acid composition had a weight average molecular weight of 175,000 and a melting point of 176 ° C. Further, there was no isocyanate odor at the exit of the ruder after kneading. When the resin filter at the outlet of the extruder was confirmed, no foreign matter due to thermal modification of the cyclic carbodiimide (CC2) was found.

[Example 2]
In Example 1, when the reaction was carried out in the same manner except that the cyclic carbodiimide (CC2) was changed to the cyclic carbodiimide (CC1), the carboxyl end group concentration was reduced to 0.7 equivalent / ton or less. The resulting polylactic acid had a weight average molecular weight of 180,000 and a melting point of 174 ° C. Further, there was no isocyanate odor at the exit of the ruder after kneading. When the resin filter at the outlet of the extruder was confirmed, no foreign matter due to thermal modification of the cyclic carbodiimide (CC1) was found.

[Example 3]
In Example 1, when the polylactic acid composition obtained by the operation of Production Example 4 was changed to the polylactic acid composition obtained by the operation of Production Example 5, the same operation was carried out to obtain a reaction. The carboxyl end group concentration of the obtained polylactic acid composition was reduced to 0.5 equivalent / ton or less. The resulting polylactic acid composition had a weight average molecular weight of 173,000 and a melting point of 174 ° C. Further, there was no isocyanate odor at the exit of the ruder after kneading. When the resin filter at the outlet of the extruder was confirmed, no foreign matter due to thermal modification of the cyclic carbodiimide (CC2) was found.

[Example 4]
In Example 1, the cyclic carbodiimide (CC2) was converted to the cyclic carbodiimide (CC3), the polylactic acid composition obtained by the operation of Production Example 4 was converted to the stereocomplex polylactic acid composition obtained by the operation of Production Example 6, and biaxial extrusion When the reaction was carried out in the same manner except that the temperature of the machine was changed to 180 to 260 ° C., the carboxyl end group concentration of the obtained polylactic acid composition was reduced to 0.3 equivalent / ton or less. The resulting polylactic acid had a weight average molecular weight of 152,000 and a melting point of 220 ° C. Further, there was no isocyanate odor at the exit of the ruder after kneading. When the resin filter at the outlet of the extruder was confirmed, no foreign matter due to thermal modification of the cyclic carbodiimide (CC3) was found.

[Example 5]
In Example 4, the stereocomplex polylactic acid composition obtained by the operation of Production Example 6 was obtained as the polylactic acid composition obtained by the operation of Production Example 4, and the polylactic acid composition obtained by the operation of Production Example 5 was 1: 1. When the reaction was carried out in the same manner except that 0.3 parts by weight of a phosphate ester metal salt (“ADEKA STAB” NA-11 manufactured by ADEKA Co., Ltd.) was added at the preceding stage of the extruder, The carboxyl end group concentration of the lactic acid composition decreased to 0.2 equivalent / ton or less. The resulting polylactic acid had a weight average molecular weight of 155,000 and a melting point of 219 ° C. Further, there was no isocyanate odor at the exit of the ruder after kneading. When the resin filter at the outlet of the extruder was confirmed, no foreign matter due to thermal modification of the cyclic carbodiimide (CC3) was found.

[Example 6]
In Example 4, the same method was used except that the polylactic acid composition obtained by the operation of Production Example 6 was changed to the stereocomplex polylactic acid composition obtained by the operation of Production Example 8. The carboxyl end group concentration of the obtained polylactic acid composition was reduced to 0.3 equivalent / ton or less. The resulting polylactic acid composition had a weight average molecular weight of 160,000 and a melting point of 210 ° C. Further, there was no isocyanate odor at the exit of the ruder after kneading. When the resin filter at the outlet of the extruder was confirmed, no foreign matter due to thermal modification of the cyclic carbodiimide (CC3) was found.

[Example 7]
In Example 1, when the reaction was carried out in the same manner except that the polylactic acid composition obtained by the operation of Production Example 7 was used instead of the polylactic acid composition of Production Example 4, the carboxyl end group concentration was 0.00. It decreased to 7 equivalents / ton or less. The resulting polylactic acid composition had a weight average molecular weight of 220,000 and a melting point of 154 ° C. Further, there was no isocyanate odor at the exit of the ruder after kneading. When the resin filter at the outlet of the extruder was confirmed, no foreign matter due to thermal denaturation of the cyclic carbodiimide compound (CC1) was found.

[Examples 8 to 11]
In Example 4, it carried out by the same operation except having changed the addition amount of the cyclic carbodiimide compound (CC3) to 0.5-6 weight part. The results are shown in Table 1.

[Comparative Example 1]
In Example 1, the cyclic carbodiimide compound (CC2) was replaced with linear carbodiimide manufactured by Rhein Chemie Japan Co., Ltd., “STABAXOL” I, and reacted under the same conditions except that the carboxyl end group concentration was 0. The equivalent malodor of isocyanate was strongly generated at the exit of the ruder.

[Comparative Example 2]
In Example 4, the cyclic carbodiimide compound (CC3) was replaced with a linear polycarbodiimide compound [Nisshinbo Chemical Co., Ltd .; “Carbodilite” HMV-8CA], and other conditions were reacted in the same manner. Although the concentration was 0.6 equivalent / ton, a strong malodor of isocyanate was generated at the outlet of the ruder.

[Example 12]
The pellets obtained in Example 4 were dried for 12 hours in a vacuum dryer set at 110 ° C. The dried chip was melt-extruded into a 210 μm film at a die temperature of 220 ° C., and adhered and solidified to the surface of the mirror-cooled drum by electrostatic casting using a platinum-coated linear electrode.
The unstretched film is further 100 ° C., stretched 1.1 to 1.5 times in the longitudinal direction, 1.1 to 2.0 times in the transverse direction, and further heat-set at 140 to 160 ° C. to a thickness of about 40 μm. A biaxially stretched film was obtained. An irritating odor derived from isocyanate gas was not felt in the process of film formation, stretching and heat setting.

[Example 13]
The pellets obtained in Example 4 were dried with a dehumidifying dryer at 50 ° C., melted at a temperature of 220 ° C. with an extruder-type spinning machine, and a spinneret having 36 holes of 0.27 φmm was used. After spinning at a discharge rate of 8.35 g / min, the undrawn yarn was wound up at a speed of 500 m / min. The wound undrawn yarn was drawn 4.9 times with a drawing machine at 80 ° C. by preheating to wind the drawn yarn, and then heat treated at 130 ° C. The process passability in the spinning process and the drawing process was good, and the wound drawn yarn was a multifilament with a fineness of 167 dTex / 36 fil, a strength of 3.7 cN / dTex, an elongation of 35%, and a melting point of 213 ° C. . Moreover, it had a single melting peak in DSC measurement, the melting peak temperature (melting point) was 224 ° C., and the stereocomplex crystallinity was 100%.
The obtained stereocomplex polylactic acid filament was twisted at 80 T / m (twisting coefficient 6.2), and then placed on warps and wefts to weave a twill-woven fabric. After dry heat setting at 2 ° C. for 2 minutes, dyeing was performed at a temperature of 110 ° C. for 20 minutes using a liquid dyeing machine. At that time, a black disperse dye was used. Furthermore, a dry heat set at a temperature of 130 ° C. for 2 minutes was performed to obtain a woven fabric having a warp density of 124 yarns / 2.54 cm and a weft density of 93 yarns / 2.54 cm.
Generation of isocyanate odor was not felt during melt-kneading, yarn production and weaving. Moreover, when the obtained textile fabric was melted at 300 ° C. for 5 minutes, the isocyanate odor evaluation was acceptable.

[Example 14]
The pellets obtained in Example 4 were dried with a dehumidifying dryer at 50 ° C., mixed and spun at 220 ° C. with a discharge rate of 8.35 g / min with an extruder-type spinning machine, and then at a speed of 500 m / min. Undrawn yarn was wound up. The wound undrawn yarn was drawn 4.9 times with a drawing machine at 80 ° C. by preheating to wind the drawn yarn, and then heat treated at 180 ° C. The processability in the spinning process and the drawing process was good, and the wound drawn yarn was a multifilament having a fineness of 167 dTex / 36 fil, a strength of 3.6 cN / dTex, an elongation of 36%, and a melting point of 219 ° C. . Moreover, it had a single melting peak in DSC measurement, the melting peak temperature (melting point) was 222 ° C., and the stereocomplex crystallization rate was 100%.
After knitting a tentacle knitted fabric using the obtained stereocomplex polylactic acid filament, the knitted fabric was set at 150 ° C. for 2 minutes by dry heat, and then 20 ° C. at 120 ° C. using a liquid dyeing machine. Minute staining was performed. At that time, a black disperse dye was used. Furthermore, a dry heat set at a temperature of 160 ° C. for 2 minutes was performed.
Generation of isocyanate odor was not felt during melt-kneading, yarn production and knitting. Moreover, when the obtained textile fabric was melted at 300 ° C. for 5 minutes, the isocyanate odor evaluation was acceptable.
Further, the carboxyl end group concentration of the polylactic acid filament immediately after spinning was 1 equivalent / ton, and the carboxyl end group concentration of the polylactic acid structure was 1 equivalent / ton.

[Example 15]
The pellets obtained in Example 4 were dried with a dehumidifying dryer at 50 ° C., melted at 220 ° C. with an extruder type spinning machine, spun from the pores, and then spun at a spinning speed of 4300 m / min with an ejector. Then, the web collected on the moving net conveyor is thermocompression bonded with an embossing roll and a flat roll having a convex area of 16% under the conditions of a temperature of 160 ° C. and a linear pressure of 25 kg / cm. A spunbonded nonwoven fabric having a fineness of 1.6 dtex and a basis weight of 30 g / m ² was produced.
Generation of isocyanate odor was not felt during melt-kneading, yarn production and spunbond production. Moreover, when the obtained textile fabric was melted at 300 ° C. for 5 minutes, the isocyanate odor evaluation was acceptable.
Further, the carboxyl end group concentration of the polylactic acid filament immediately after spinning was 1 equivalent / ton, and the carboxyl end group concentration of the polylactic acid structure was 2 equivalent / ton.

[Example 16]
The pellets obtained in Example 4 were dried with a dehumidifying dryer at 50 ° C., and a test piece was prepared with an injection molding machine at a nozzle of 220 ° C. and a mold temperature of 110 ° C.
Generation of isocyanate odor was not felt during melt-kneading and injection molding. Moreover, when the obtained test piece was melted at 300 ° C. for 5 minutes, the isocyanate odor evaluation was acceptable.
Further, the carboxyl end group concentration of the molded product was 1 equivalent / ton.

Claims (24)

A polylactic acid composition comprising a polylactic acid (A) component as a main component, wherein the polylactic acid (A) component is 95 wt% or more and 99.99 wt% or less based on the resin composition, and α- other than lactic acid The hydroxycarboxylic acid (B) component is 0.01% by weight or more and 5% by weight or less, and the carbodiimide compound (C) represented by the following structural formula is added per 100% by weight of the total amount of the components (A) and (B) A polylactic acid composition comprising 0.01 to 10% by weight.

(In the formula, Q represents a divalent organic group.) The polylactic acid composition according to claim 1, wherein the α-hydroxycarboxylic acid (B) component other than lactic acid is a component derived from a compound represented by the following structural formula.

(In the formula, R ′ represents a hydrogen atom or an aliphatic alkyl group.)   The polylactic acid composition according to claim 1, comprising a poly L-lactic acid component and a poly D-lactic acid component as the polylactic acid (A) component.   The polylactic acid composition according to claim 3, which shows a crystal melting peak of a stereocomplex phase polylactic acid at 190 ° C. or higher in differential scanning calorimetry measurement. The polylactic acid composition according to claim 4, wherein the stereocomplex crystallinity (S) defined by the following formula is 90 to 100%.
S = [ΔHms / (ΔHmh + ΔHms)] × 100
(However, ΔHms = Crystal melting enthalpy of stereocomplex phase polylactic acid and ΔHmh = Polylactic acid homophase crystal melting enthalpy) The polylactic acid composition according to claim 1, wherein Q in the carbodiimide compound (C) is a divalent to tetravalent linking group represented by the following formula (1-1), (1-2) or (1-3). object.

(In the formula, Ar ¹ and Ar ² are each independently a divalent to tetravalent aromatic group having 5 to 15 carbon atoms, and may contain a hetero atom or a substituent. R ¹ and R ² each represent Independently, an aliphatic group having 2 to 4 carbon atoms and 1 to 20 carbon atoms, an alicyclic group having 2 to 4 carbon atoms and a combination thereof, or these aliphatic groups, alicyclic groups and 2 A combination of a tetravalent aromatic group having 5 to 15 carbon atoms and optionally containing a heteroatom or a substituent, and X ¹ and X ² are each independently 2 to 4 carbon atoms having 1 to 20 carbon atoms. An aliphatic group having 2 to 4 carbon atoms, an alicyclic group having 3 to 20 carbon atoms, an aromatic group having 2 to 4 carbon atoms and a combination thereof, and includes a hetero atom and a substituent. S is an integer of 0 to 10. k is an integer of 0 to 10. When s or k is 2 or more, s is an integer. ^{X 1} or ^{X 2,} of the unit and the other ^{X 1,} or ^{X 2} and good .X ³ be different, a divalent to tetravalent aliphatic group having 1 to 20 carbon atoms, a divalent to tetravalent The alicyclic group having 3 to 20 carbon atoms, the aromatic group having 2 to 4 carbon atoms and the combination thereof, which may contain a hetero atom or a substituent, and Q is When it is a divalent linking group, Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² and X ³ are all divalent groups, and when Q is a trivalent linking group , Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² and X ³ are trivalent groups, and when Q is a tetravalent linking group, Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² and X ³ are tetravalent groups or two are trivalent groups.) The polylactic acid composition according to claim 1, wherein the carbodiimide compound (C) is a compound represented by the following formula (2).

(Wherein Q _a is a divalent linking group that is an aliphatic group, an alicyclic group, an aromatic group, or a combination thereof, and may contain a hetero atom or a substituent.) The polylactic acid composition according to claim 7, wherein Q _a is a divalent linking group represented by the following formula (2-1), (2-2), or (2-3).

(In the formula, Ar _a ¹ , Ar _a ² , R _a ¹ , R _a ² , X _a ¹ , X _a ² , X _a ³ , s and k are represented by the formulas (1-1) to (1-3), respectively. ^{Ar 1, Ar 2, R 1} , R 2, X 1, is the same as ^{X 2,} X ^3, s and k in.) The polylactic acid composition according to claim 7, wherein the carbodiimide compound (C) is a compound represented by the following formula (2-1-1).

(In the formula, Ar _a ¹ and Ar _a ² are each an independently substituted arylene group having 5 to 15 carbon atoms. X _a ¹ is an alkylene group having 1 to 20 carbon atoms. ) The polylactic acid composition according to claim 7, wherein the carbodiimide compound (C) is a compound represented by the following formula (2-1-1a).

(In the formula, R ^q and R ^r each independently represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms. X _a ¹ is an alkylene group having 1 to 20 carbon atoms.) The polylactic acid composition according to claim 1, wherein the carbodiimide compound (C) is a compound represented by the following formula (3).

(Wherein, Q _b is an aliphatic group, an alicyclic group, an aromatic group or a trivalent linking group combinations thereof, heteroatoms, which may contain a substituent .Y is annular It is a carrier carrying the structure.) The polylactic acid composition according to claim 11, wherein Q _b is a trivalent linking group represented by the following formula (3-1), (3-2), or (3-3).

(In the formula, Ar _b ¹ , Ar _b ² , R _b ¹ , R _b ² , X _b ¹ , X _b ² , X _b ³ , s and k are represented by the formulas (1-1) to (1-3), respectively. Are the same as Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² , X ³ , s, and k, with one of these being a trivalent group.)   The polylactic acid composition according to claim 11, wherein Y is a single bond, a double bond, an atom, an atomic group or a polymer. The lactic acid composition according to claim 1, wherein the carbodiimide compound (C) is a compound represented by the following formula (4).

(Wherein Q _c is a tetravalent linking group which is an aliphatic group, an aromatic group, an alicyclic group or a combination thereof, and may contain a hetero atom or a substituent. Z ¹ and Z ² is a carrier carrying a ring structure.) The polylactic acid composition according to claim 14, wherein Q _c is a tetravalent linking group represented by the following formula (4-1), (4-2), or (4-3).

(In the formula, Ar _c ¹ , Ar _c ² , R _c ¹ , R _c ² , X _c ¹ , X _c ² , X _c ³ , s and k are respectively represented by formulas (1-1) to (1-3) Are the same as Ar ¹ , Ar ² , R ¹ , R ² , X ¹ , X ² , X ³ , s and k, provided that one of them is a tetravalent group or two are 3 Valent group.) The polylactic acid composition according to claim 14, wherein Z ¹ and Z ² are each independently a single bond, a double bond, an atom, an atomic group or a polymer. The polylactic acid composition according to claim 16, wherein the carbodiimide compound (C) is a compound represented by the following formula (4-1-1).

_{(Wherein, .Ar} ^{c 1} _X ^c 1 is alkanetetrayl group having 1 to 20 carbon ^{_{atoms, Ar c 2, Ar c 3}} , Ar c 4 may be substituted independently, the number of carbon atoms 5 to 15 arylene groups.) The polylactic acid composition according to claim 16, wherein the carbodiimide compound (C) is a compound represented by the following formula (4-1-1c).

(Wherein, X _c ¹ is an alkanetetrayl group having 1 to 20 carbon atoms. R ^q , R ^r , R ^s and R ^t are each independently a hydrogen atom or an alkyl group having 1 to 20 carbon atoms. .)   A molded body selected from the group consisting of a fiber, a film, and a molded product obtained by molding the polylactic acid composition according to claim 1.   A fiber structure partially including the fiber according to claim 19.   The film structure which contains the film of Claim 19 in part.   The fiber structure which contains the resin composition of any one of Claims 1-18 in part.   The film structure which contains the resin composition of any one of Claims 1-18 in part.   The molded article which contains the resin composition of any one of Claims 1-18 in part.