JP7194789B2 - Articles and methods of manufacturing articles - Google Patents

Description

The present invention relates to molded articles and methods of manufacturing molded articles. In particular, the present invention relates to a molded article suitable for camera parts mounted on automobiles and a method for manufacturing the molded article.

Polyamide resins, which are representative engineering plastics, are easy to process and have excellent mechanical properties, electrical properties, heat resistance, and other physical and chemical properties. Therefore, it is widely used for vehicle parts, electrical and electronic equipment parts, and other precision equipment parts.
For example, in Patent Document 1, dicarboxylic acid units containing 60 to 100 mol% of terephthalic acid units and 1,9-diaminononane units and/or 60 to 100 mol% of 2-methyl-1,8-diaminooctane units are disclosed. A polyamide (A) having a diamine unit and a fibrous reinforcing material (B) are melt-kneaded, and the content of the polyamide (A) is 50 to 80% by mass and the content of the fibrous reinforcing material (B) A camera module barrel or holder formed by molding a polyamide composition having a content of 20 to 50% by mass, wherein the fibrous reinforcing material (B) has an average length of 300 μm or less before melt-kneading. A barrel or holder is disclosed.

JP 2010-286544 A

When the present inventor examined Patent Document 1, it was found that the mechanical strength was insufficient in Patent Document 1, although a fibrous filler was blended. In addition, precision machine parts such as camera parts are required to be less permeable to moisture. An object of the present invention is to solve such problems, and an object thereof is to provide a molded article which is excellent in mechanical strength and impermeable to moisture.

Based on the above problems, the present inventors conducted studies and found that a semi-aromatic polyamide resin having a terminal carboxyl group concentration higher than a terminal amino group concentration was used, and a fiber having a number average fiber length exceeding 300 µm was molded. The inventors have found that by forming a molded product that is made of a semi-aromatic polyamide resin and the fiber, the adhesion between the semi-aromatic polyamide resin and the fiber can be improved, the mechanical strength can be improved, and moisture can be made difficult to permeate, and the present invention has been completed. .
Specifically, the above problems have been solved by the following means <1>, preferably by <2> to <15>.
<1> Molded from a polyamide resin composition containing a semi-aromatic polyamide resin and fibers having a number average fiber length of more than 300 μm, wherein the terminal carboxyl group concentration of the semi-aromatic polyamide resin is higher than the terminal amino group concentration Molding.
<2> The molded article according to <1>, wherein the fiber is at least one selected from carbon fiber and glass fiber.
<3> The molded article according to <1> or <2>, wherein the fibers are treated with at least one of a surface treatment agent and a sizing agent.
<4> The molded article according to any one of <1> to <3>, wherein the number average fiber length of the fibers is 1.0 mm to 6.0 mm.
<5> The molded article according to any one of <1> to <4>, wherein the difference between the terminal carboxyl group concentration and the terminal amino group concentration is 40 to 100 μeq/g.
<6> The semi-aromatic polyamide resin is composed of diamine-derived structural units and dicarboxylic acid-derived structural units, and 70 mol% or more of the diamine-derived structural units are derived from xylylenediamine, and the dicarboxylic acid-derived structure The molded article according to any one of <1> to <5>, wherein 70 mol% or more of the units are derived from the α,ω-linear aliphatic dicarboxylic acid having 4 to 20 carbon atoms.
<7> The semi-aromatic polyamide resin is composed of diamine-derived structural units and dicarboxylic acid-derived structural units, and 70 mol% or more of the diamine-derived structural units are derived from xylylenediamine, and the dicarboxylic acid-derived structure The molded article according to any one of <1> to <5>, wherein 70 mol% or more of the units are derived from adipic acid.
<8> The molded article according to any one of <1> to <7>, further comprising a black colorant.
<9> The molded article according to any one of <1> to <8>, further comprising talc.
<10> Further, <1> to <7, wherein a black coloring agent and talc are included, and the mass ratio of the black coloring agent to talc (black coloring agent/talc) in the molded article is 1.5 to 2.5. The molded article according to any one of >.
<11> The molded article according to any one of <1> to <10>, which is an injection molded article.
<12> The molded article according to any one of <1> to <11>, which is a camera part.
<13> The molded article according to <12>, wherein the camera component has a maximum length of 15 to 40 mm.
<14> The molded article according to <12> or <13>, wherein the camera component contains a member derived from the polyamide resin composition, and the proportion of the member is 1 to 99% by mass.
<15> Injection molding a polyamide resin composition containing a semi-aromatic polyamide resin and fibers having a number average fiber length of more than 300 μm, wherein the terminal carboxyl group concentration of the semi-aromatic polyamide resin is higher than the terminal amino group concentration. The method for producing a molded article according to any one of <1> to <14>, comprising:

The present invention has made it possible to provide molded articles that are excellent in mechanical strength and impermeable to moisture.

1 is a schematic diagram showing a device for measuring water permeability coefficient; FIG.

The contents of the present invention will be described in detail below. In this specification, the term "~" is used to mean that the numerical values before and after it are included as the lower limit and the upper limit.

The molded article of the present invention comprises a semi-aromatic polyamide resin and fibers having a number average fiber length of more than 300 μm, and the terminal carboxyl group concentration of the semi-aromatic polyamide resin is higher than the terminal amino group concentration, a polyamide resin composition. It is characterized by being a molded article molded from.
By using a semi-aromatic polyamide resin having a terminal carboxyl group concentration higher than a terminal amino group concentration and using a fiber having a number average fiber length exceeding 300 μm, the adhesion of the semi-aromatic polyamide resin to the fiber is improved, Molded products with high mechanical strength can be obtained. Furthermore, a molded article that is difficult to permeate with moisture can be obtained.

<Semi-aromatic polyamide resin>
The molded article of the present invention contains a semi-aromatic polyamide resin.
Here, the semi-aromatic polyamide resin is composed of diamine-derived structural units and dicarboxylic acid-derived structural units, and 30 to 70 mol% of the total structural units of the diamine-derived structural units and dicarboxylic acid-derived structural units It refers to a structural unit containing an aromatic ring, and preferably 40 to 60 mol % of the total structural units of the diamine-derived structural unit and the dicarboxylic acid-derived structural unit are structural units containing an aromatic ring.

The semi-aromatic polyamide resin used in the present invention has a terminal carboxyl group concentration higher than a terminal amino group concentration. With such a configuration, the adhesion between the fibers and the semi-aromatic polyamide resin can be improved.
The difference between the terminal carboxyl group concentration and the terminal amino group concentration in the present invention is preferably 40 to 100 μeq/g. By setting it as such a range, the adhesiveness with a fiber can be improved more.
The lower limit of the difference between the terminal carboxyl group concentration and the terminal amino group concentration is preferably 45 μeq/g or more, more preferably 47 μeq/g or more. The upper limit of the difference between the terminal carboxyl group concentration and the terminal amino group concentration is preferably 90 μeq/g or less, more preferably 80 μeq/g or less, and 70 μeq/g or less. More preferably, it is 65 μeq/g or less, and even more preferably 55 μeq/g or less.
In addition, the semi-aromatic polyamide resin used in the present invention preferably has a terminal amino group concentration ([NH ₂ ]) of less than 100 μeq/g, more preferably 5 to 75 μeq/g, still more preferably 10 to 60 μeq/g. g, more preferably 20-50 μeq/g. In addition, the semi-aromatic polyamide resin used in the present invention has a terminal carboxyl group concentration ([COOH]) of preferably less than 150 μeq/g, more preferably 20 to 120 μeq/g, still more preferably 40 to 110 μeq/g. g, more preferably 50-100 μeq/g, even more preferably 75-100 μeq/g.
Furthermore, the ratio of terminal amino group concentration to terminal carboxyl group concentration ([NH ₂ ]/[COOH]) is preferably 0.7 or less, more preferably 0.6 or less, and even more preferably 0.5 or less. If the ratio is more than 0.7, it may become difficult to control the molecular weight when polymerizing the semi-aromatic polyamide resin. Although the lower limit of the ratio of terminal amino group concentration to terminal carboxyl group concentration ([NH ₂ ]/[COOH]) is not particularly defined, it may be, for example, 0.2 or more.
The terminal amino group concentration and the terminal carboxyl group concentration of the semi-aromatic polyamide resin are measured according to the methods described in Examples below. If the devices and the like described in the examples cannot be obtained due to obsolescence or the like, other devices having equivalent performance can be used. The same applies to other measurement methods hereinafter.

Semi-aromatic polyamide resins used in the present invention include polyhexamethylene terephthalamide (polyamide 6T), polyhexamethylene isophthalamide (polyamide 6I), polyamide 66/6T, polyxylylene adipamide, polyxylylene bacamide, polyxylylene dedecamide, polyamide 9T, polyamide 9MT, polyamide 6I/6T and the like.
In addition, semi-aromatic polyamide resins and the like described in paragraphs 0020 to 0058 of JP-A-2016-138163 are also preferably used.

Among the semi-aromatic polyamide resins as described above, from the viewpoint of moldability and heat resistance, it is composed of structural units derived from diamine and structural units derived from dicarboxylic acid, and 70 mol% or more of the structural units derived from diamine is xylylene. A semi-aromatic polyamide resin derived from an amine and having 70 mol% or more of the structural units derived from a dicarboxylic acid derived from an α,ω-straight-chain aliphatic dicarboxylic acid having 4 to 20 carbon atoms (hereinafter referred to as "XD-based polyamide" (sometimes) is preferred.

In the XD-based polyamide, 70 mol% or more, preferably 80 mol% or more, more preferably 90 mol% or more, and still more preferably 95 mol% or more of the diamine-derived structural units are derived from xylylenediamine, and dicarboxylic acid-derived 70 mol% or more, preferably 80 mol% or more, more preferably 90 mol%, and still more preferably 95 mol% or more of the structural units are derived from α,ω-linear aliphatic dicarboxylic acid having 4 to 20 carbon atoms do.
The xylylenediamine is preferably para-xylylenediamine, meta-xylylenediamine, or a mixture of both, and more preferably includes at least meta-xylylenediamine.

Examples of diamines other than meta-xylylenediamine and para-xylylenediamine that can be used as raw material diamine components for XD-based polyamides include tetramethylenediamine, pentamethylenediamine, 2-methylpentanediamine, hexamethylenediamine, heptamethylenediamine, octamethylenediamine, and octamethylenediamine. Aliphatic diamines such as methylenediamine, nonamethylenediamine, decamethylenediamine, dodecamethylenediamine, 2,2,4-trimethyl-hexamethylenediamine, 2,4,4-trimethylhexamethylenediamine, 1,3-bis(amino methyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane, 1,3-diaminocyclohexane, 1,4-diaminocyclohexane, bis(4-aminocyclohexyl)methane, 2,2-bis(4-aminocyclohexyl)propane , alicyclic diamines such as bis(aminomethyl)decalin and bis(aminomethyl)tricyclodecane, diamines having aromatic rings such as bis(4-aminophenyl) ether, paraphenylenediamine, bis(aminomethyl)naphthalene, etc. can be exemplified, and can be used alone or in combination of two or more.
When a diamine other than xylylenediamine is used as the diamine component, it is preferably less than 20 mol %, more preferably 10 mol % or less, of the constituent units derived from the diamine.

Examples of α,ω-straight-chain aliphatic dicarboxylic acids having 4 to 20 carbon atoms that are preferable for use as the starting dicarboxylic acid component of the semiaromatic polyamide resin include succinic acid, glutaric acid, pimelic acid, suberic acid, azelaic acid, Aliphatic dicarboxylic acids such as adipic acid, sebacic acid, undecanedioic acid, and dodecanedioic acid can be exemplified, and one or a mixture of two or more thereof can be used. Adipic acid or sebacic acid is preferred, and adipic acid is more preferred, since it is in a range suitable for

Examples of dicarboxylic acid components other than the α,ω-straight-chain aliphatic dicarboxylic acids having 4 to 20 carbon atoms include phthalic acid compounds such as isophthalic acid, terephthalic acid and orthophthalic acid, 1,2-naphthalenedicarboxylic acid, 1,3 -naphthalenedicarboxylic acid, 1,4-naphthalenedicarboxylic acid, 1,5-naphthalenedicarboxylic acid, 1,6-naphthalenedicarboxylic acid, 1,7-naphthalenedicarboxylic acid, 1,8-naphthalenedicarboxylic acid, 2,3-naphthalene Naphthalenedicarboxylic acids such as isomers such as dicarboxylic acids, 2,6-naphthalenedicarboxylic acid and 2,7-naphthalenedicarboxylic acid can be exemplified, and can be used singly or in combination of two or more. When using a dicarboxylic acid component other than the α,ω-straight-chain aliphatic dicarboxylic acid having 4 to 20 carbon atoms, it is preferably less than 20 mol% of the structural units derived from the dicarboxylic acid, and is preferably 10 mol% or less. more preferred.

The semi-aromatic polyamide resin is mainly composed of diamine-derived structural units and dicarboxylic acid-derived structural units, but does not completely exclude structural units other than these. It goes without saying that structural units derived from aliphatic aminocarboxylic acids such as lactams such as lactams such as aminocaproic acid and aminoundecanoic acid may be included. In the present invention, the sum of diamine-derived structural units and dicarboxylic acid-derived structural units in the semi-aromatic polyamide resin preferably accounts for 90% or more, more preferably 95% or more, of all structural units.

The melting point of the semi-aromatic polyamide resin is preferably 150 to 350°C, more preferably 180 to 330°C, even more preferably 200 to 300°C.
Also, the glass transition temperature of the semi-aromatic polyamide resin is preferably 50 to 150°C, more preferably 55 to 120°C, and particularly preferably 60 to 100°C. Within this range, the heat resistance of the molded product tends to be better.

The melting point of the semi-aromatic polyamide resin is measured as the peak top temperature of the endothermic peak during temperature rise observed by DSC (differential scanning calorimetry). The glass transition temperature of the semi-aromatic polyamide resin is measured as the peak top temperature obtained by once heating and melting the semi-aromatic polyamide resin to eliminate the influence of the heat history on the crystallinity, and then raising the temperature again.
Specifically, using a DSC measuring instrument, the amount of the semi-aromatic polyamide resin as a sample was about 1 mg, nitrogen was flowed at 30 mL / min as the atmosphere gas, and the temperature increase rate was 10 ° C. / min. The melting point is determined from the peak top temperature of the endothermic peak observed when the material is melted by heating from room temperature to a temperature higher than the expected melting point. Next, the molten semi-aromatic polyamide resin is rapidly cooled with dry ice, heated again to a temperature above the melting point at a rate of 10° C./min, and the glass transition temperature is determined. The DSC measuring instrument includes DSC-60 manufactured by SHIMADZU CORPORATION.

The semi-aromatic polyamide resin preferably has a number average molecular weight (Mn) of 6,000 to 30,000, more preferably 8,000 to 28,000, still more preferably 9,000 to 26,000. , more preferably 10,000 to 24,000, and even more preferably 11,000 to 22,000. Within such a range, heat resistance, elastic modulus, dimensional stability, and moldability are improved.

The number average molecular weight (Mn) referred to here is defined by the terminal amino group concentration [NH ₂ ] (μ equivalent/g) and the terminal carboxyl group concentration [COOH] (μ equivalent/g) of the semi-aromatic polyamide resin. It is calculated by the following formula.
Number average molecular weight (Mn) = 2,000,000/([COOH] + [ _NH2 ])

The semi-aromatic polyamide resin preferably has a molecular weight distribution (weight average molecular weight/number average molecular weight (Mw/Mn)) of 1.8 to 3.1. The molecular weight distribution is more preferably 1.9-3.0, more preferably 2.0-2.9. By setting the molecular weight distribution within such a range, there is a tendency to easily obtain a three-dimensional structure having excellent mechanical properties.
The molecular weight distribution of the semi-aromatic polyamide resin can be adjusted, for example, by appropriately selecting the species and amounts of initiators and catalysts used during polymerization and polymerization reaction conditions such as reaction temperature, pressure and time. It can also be prepared by mixing a plurality of types of semi-aromatic polyamide resins with different average molecular weights obtained under different polymerization conditions, or by separating and precipitating the semi-aromatic polyamide resins after polymerization.

The molecular weight distribution can be determined by GPC measurement, specifically, as an apparatus "HLC-8320GPC" manufactured by Tosoh Corporation, as a column, two "TSK gel Super HM-H" manufactured by Tosoh Corporation are used, and an eluent is used. As, hexafluoroisopropanol (HFIP) with a sodium trifluoroacetate concentration of 10 mmol / L, a resin concentration of 0.02% by mass, a column temperature of 40 ° C., a flow rate of 0.3 mL / min, and a refractive index detector (RI). , can be obtained as a value in terms of standard polymethyl methacrylate (PMMA). A calibration curve is prepared by dissolving 6 levels of PMMA in HFIP and measuring.

The lower limit of the content of the semi-aromatic polyamide resin in the molded article of the present invention is preferably 25% by mass or more, more preferably 30% by mass or more, and further preferably 40% by mass or more. It is more preferably 50% by mass or more, and even more preferably 55% by mass or more. The upper limit of the content is preferably 75% by mass or less, more preferably 70% by mass or less.
The molded article of the present invention may contain only one type of semi-aromatic polyamide resin, or may contain two or more types. When two or more types are included, the total amount is preferably within the above range.

In the molded article of the present invention, the total amount of the semi-aromatic polyamide resin and the filler containing fibers described below preferably accounts for 90% by mass or more of the entirety.

<Other polyamide resins>
The molded article of the present invention may contain one or more polyamide resins other than the semi-aromatic polyamide resin. Such polyamide resins include polyamide 4, polyamide 6, polyamide 11, polyamide 12, polyamide 46, polyamide 66, polyamide 610, polyamide 612 and the like.
Of course, in the present invention, the configuration may be such that these other polyamide resins are not substantially included. "Substantially free" means that the content of the other polyamide resin is 2% by mass or less of the content of the semi-aromatic polyamide resin contained in the molded article of the present invention, preferably 1% by mass or less. , 0.1% by mass or less is more preferable.

<Fiber>
The molded article of the present invention contains fibers.
The fibers are not particularly limited as long as the number average fiber length exceeds 300 μm, and known fibers can be used. The lower limit of the number average fiber length of the fibers is preferably 500 μm or longer, more preferably 1.0 mm or longer, even more preferably 2.0 mm or longer, and still more preferably 3.0 mm or longer. The upper limit of the number average fiber length of the fibers is preferably 6.0 mm or less, more preferably 5.0 mm or less, and even more preferably 4.0 mm or less.

The type of fiber is not particularly limited, but inorganic fibers such as glass fiber, carbon fiber, vegetable fiber (including kenaf, bamboo fiber, etc.), alumina fiber, boron fiber, ceramic fiber, metal fiber (steel fiber, etc.). , and organic fibers such as aramid fibers, polyoxymethylene fibers, polyparaphenylenebenzobisoxazole fibers, and ultra-high molecular weight polyethylene fibers. Among them, it is preferably at least one selected from carbon fiber, aramid fiber and glass fiber, more preferably at least one selected from carbon fiber and glass fiber, and at least one selected from glass fiber. One type is more preferable.

The glass fiber has a glass composition such as A glass, C glass, E glass, S glass, etc. E glass (alkali-free glass) is particularly preferable. Only one kind of glass fiber may be contained, or two or more kinds thereof may be contained.

The fiber used in the present invention may be a single fiber or a plurality of twisted single fibers.
The fibers used in the present invention are preferably treated with at least one of a surface treatment agent and a sizing agent. Examples of surface treatment agents include coupling agents such as silane-based coupling agents, titanium-based coupling agents, and aluminate-based coupling agents. Examples of sizing agents include epoxy-based compounds, urethane-based compounds, carboxylic acid-based compounds, urethane/maleic acid-modified compounds, and urethane/amine-modified compounds. By using a surface treatment agent and/or a sizing agent, the adhesion to the semi-aromatic polyamide resin can be further improved, and the mechanical strength of the molded article of the present invention can be further improved.

The lower limit of the content of the fibers used in the present invention is preferably 25% by mass or more, more preferably 26% by mass or more, and even more preferably 28% by mass or more. The upper limit of the content is preferably 75% by mass or less, more preferably 65% by mass or less, further preferably 55% by mass or less, and even more preferably 45% by mass or less, It is more preferably 35% by mass or less.
The molded article of the present invention may contain only one type of fiber, or may contain two or more types. When two or more kinds are included, the total amount is preferably within the above range.

<Other fillers>
The molded article of the present invention may contain other fillers in addition to the fibers having a number average fiber length exceeding 300 μm. Other fillers include fibers having a number average fiber length of 300 μm or less.
In addition, in the molded article of the present invention, the content of filler other than the fibers having a number average fiber length exceeding 300 μm is preferably 10% by mass or less of the fibers having a number average fiber length exceeding 300 μm, and 5 mass % or less, more preferably 3 mass % or less, and even more preferably 1 mass % or less. By setting it as such a range, there exists a tendency for the effect of this invention to be exhibited more effectively.

<Black colorant>
The molded article of the present invention may contain a black colorant. By blending a black colorant, a molded article having excellent light-shielding properties can be obtained.
Carbon black is exemplified as the black colorant used in the present invention. Details of carbon black can be referred to the description in paragraph 0021 of JP-A-2011-57977, and the contents thereof are incorporated herein.
Further, when a black colorant such as carbon black is blended into the molded article of the present invention, it is preferable to knead it with the semi-aromatic polyamide resin after forming a masterbatch. For details of the masterbatch, reference can be made to paragraphs 0038 to 0042 of JP-A-2011-57977, the contents of which are incorporated herein.
Furthermore, when producing the molded article of the present invention by laser welding, it is also preferable to use a light-transmitting black colorant. The light-transmissive black colorant is a colorant with high transmittance in the wavelength range of the irradiated laser light, for example, the wavelength range of 800 nm to 1064 nm. Specific examples include nigrosine, naphthalocyanine, aniline black, phthalocyanine, porphyrin, perylene, perinone, quaterrylene, azo dyes, anthraquinone, squaric acid derivatives, and immonium dyes. Examples of commercially available products include e-Bind ACW-9871 and e-BIND LTW-8731H, which are colorants manufactured by Orient Chemical Industry Co., Ltd.
When the molded article of the present invention contains a black colorant, its content is preferably 0.1 to 10 parts by mass, and 0.5 to 8 parts by mass with respect to 100 parts by mass of the semi-aromatic polyamide resin. More preferably, 1 to 6 parts by mass is even more preferable.
The molded article of the present invention may contain only one kind of black colorant, or may contain two or more kinds thereof. When two or more types are included, the total amount is preferably within the above range.

<Talc>
Molded articles of the present invention may contain talc. In the present invention, crystallization can be promoted by blending talc.
The amount of talc compounded in the molded article of the present invention is preferably 0.05 to 20% by mass, more preferably 0.1 to 10% by mass, and more preferably 0.15 to 5% by mass. % by mass is more preferred, and 0.2 to 2% by mass is even more preferred. Only one type of talc may be used, or two or more types may be used in combination. When two or more kinds are used, the total amount is preferably within the above range.

In the present invention, it is particularly preferable that a black coloring agent and talc are included, and the mass ratio of the black coloring agent and talc (black coloring agent/talc) in the molded article is 1.5 to 2.5. It is more preferably 8 to 2.2. Such a range promotes the crystallization of the semi-aromatic polyamide resin and provides a molded product with excellent light-shielding properties.

<Release agent>
The molded article of the present invention may contain a release agent. Release agents include, for example, aliphatic carboxylic acids, salts of aliphatic carboxylic acids, esters of aliphatic carboxylic acids and alcohols, aliphatic hydrocarbon compounds having a number average molecular weight of 200 to 15,000, and polysiloxane-based silicone oils. etc.

Aliphatic carboxylic acids include, for example, saturated or unsaturated aliphatic monovalent, divalent or trivalent carboxylic acids. Here, the aliphatic carboxylic acid also includes alicyclic carboxylic acid. Among these, preferred aliphatic carboxylic acids are monovalent or divalent carboxylic acids having 6 to 36 carbon atoms, more preferably aliphatic saturated monovalent carboxylic acids having 6 to 36 carbon atoms. Specific examples of such aliphatic carboxylic acids include palmitic acid, stearic acid, caproic acid, capric acid, lauric acid, arachidic acid, behenic acid, lignoceric acid, cerotic acid, melissic acid, tetratriacontanoic acid, montanic acid, and adipine. acid, azelaic acid, and the like. Examples of salts of aliphatic carboxylic acids include sodium salts, potassium salts, calcium salts, and magnesium salts.

As the aliphatic carboxylic acid in the ester of aliphatic carboxylic acid and alcohol, for example, the same aliphatic carboxylic acid as mentioned above can be used. Alcohols, on the other hand, include, for example, saturated or unsaturated monohydric or polyhydric alcohols. These alcohols may have substituents such as fluorine atoms and aryl groups. Among these, monohydric or polyhydric saturated alcohols having 30 or less carbon atoms are preferable, and aliphatic or alicyclic saturated monohydric alcohols or saturated aliphatic polyhydric alcohols having 30 or less carbon atoms are more preferable.

Specific examples of such alcohols include octanol, decanol, dodecanol, stearyl alcohol, behenyl alcohol, ethylene glycol, diethylene glycol, glycerin, pentaerythritol, 2,2-dihydroxyperfluoropropanol, neopentylene glycol, ditrimethylolpropane, dipentaerythritol, and the like. are mentioned.

Specific examples of esters of aliphatic carboxylic acids and alcohols include beeswax (a mixture containing myricyl palmitate as a main component), stearyl stearate, behenyl behenate, stearyl behenate, glycerin monopalmitate, glycerin monostea glycerin distearate, glycerin tristearate, pentaerythritol monopalmitate, pentaerythritol monostearate, pentaerythritol distearate, pentaerythritol tristearate, pentaerythritol tetrastearate and the like.

Examples of aliphatic hydrocarbons having a number average molecular weight of 200 to 15,000 include liquid paraffin, paraffin wax, microwax, polyethylene wax, Fischer-Tropsch wax, and α-olefin oligomers having 3 to 12 carbon atoms. In addition, an alicyclic hydrocarbon is also contained as an aliphatic hydrocarbon here. Also, the number average molecular weight of the aliphatic hydrocarbon is preferably 5,000 or less.
Among these, paraffin wax, polyethylene wax, or partial oxides of polyethylene wax are preferable, and paraffin wax and polyethylene wax are more preferable.

When the molded product of the present invention contains a mold release agent, the content of the mold release agent is preferably 0.001 to 2% by mass, more preferably 0.01 to 1% by mass, relative to the molded product. more preferred. Only one release agent may be used, or two or more release agents may be used. When two or more kinds are included, the total amount is preferably within the above range. By setting the content of the release agent within the above range, it is possible to suppress deterioration in hydrolysis resistance while sufficiently maintaining the effect of release properties, and to effectively suppress mold contamination during injection molding. .

<Other additives>
The molded article of the present invention may contain other additives generally used in polyamide resins, in addition to the above, as long as the gist of the present invention is not impaired. Such other additives include resins other than polyamide resins, lubricants, stabilizers, flame retardants, fluorescent bleaches, plasticizers, antioxidants, ultraviolet absorbers, antistatic agents, fluidity improvers, and the like. is exemplified. The total content of other additives is preferably 5% by mass or less of the molded product. Details of these additives can be referred to JP-A-2011-57977 and JP-A-2015-129244, the contents of which are incorporated herein.
Other resins include polyester resins, polyphenylene sulfide resins, polyphenylene ether resins, polycarbonate resins, polyarylate resins, phenolic resins, epoxy resins, and the like.

The polyamide resin composition constituting the molded article of the present invention is molded to a thickness of 1 mm and has a moisture permeability coefficient of 3.0 g mm / It is preferably day·m ² or less, more preferably 1.5 g·mm/day·m ² or less. The lower limit of the water permeability coefficient is preferably 0 g·mm/day·m ² , but 0.2 g·mm/day·m ² or more is sufficiently practical. The water permeability coefficient is a value measured by the method described in Examples.
Incidentally, even if the water absorption of the polyamide resin is low, it cannot be said that the water permeability coefficient is small. This is because polyamide resins have different water absorption speeds and diffusion speeds.

The molded article of the present invention can be applied to various storage containers having transparent members, electric and electronic equipment parts, office automation (OA) equipment parts, household appliance parts, machine mechanism parts, vehicle mechanism parts, and the like. In particular, it is preferably used as a camera component. As camera parts, they are used as barrels, holders, and housings. In particular, the molded article of the present invention is preferably used as a camera component for a vehicle-mounted camera.
When the molded article of the present invention is a camera part, the maximum length is preferably 15-40 mm. With such a configuration, a camera component having a balance between performance and appearance can be obtained.
When the molded article of the present invention is a camera part, it preferably contains a member derived from the polyamide resin composition, and the proportion of the member is 1 to 99% by mass. With such a configuration, it is possible to reduce the weight of the camera component and to obtain a molded product having an excellent balance between the strength of the camera component.
In particular, the molded article of the present invention is preferably an injection molded article. Of course, it goes without saying that the molded article of the present invention may be a molded article other than an injection molded article.

Next, the method for manufacturing the molded product of the present invention will be described.
The method for producing a molded article of the present invention includes a semi-aromatic polyamide resin and a fiber having a number average fiber length of more than 300 μm, and the terminal carboxyl group concentration of the semi-aromatic polyamide resin is higher than the terminal amino group concentration. Including injection molding the resin composition. The details of the semi-aromatic polyamide resin, fibers, etc. are the same as described above.
The temperature during injection molding is preferably 260 to 300°C.
In the present invention, the method for producing the polyamide resin composition is not particularly defined, and widely known methods for producing thermoplastic resin compositions can be employed. Specifically, each component is mixed in advance using various mixers such as a tumbler and Henschel mixer, and then melt-kneaded with a Banbury mixer, roll, Brabender, single screw extruder, twin screw extruder, kneader, etc. A polyamide resin composition can be produced by

Further, for example, the polyamide resin composition can be produced without pre-mixing the respective components, or pre-mixing only some of the components, supplying the mixture to an extruder using a feeder, and melt-kneading it. .
Furthermore, for example, a resin composition obtained by pre-mixing some components, supplying them to an extruder, and melt-kneading them is used as a masterbatch, and this masterbatch is mixed again with the remaining components and melt-kneaded. Polyamide resin compositions can also be produced.

EXAMPLES The present invention will be described more specifically with reference to examples below. The materials, usage amounts, ratios, processing details, processing procedures, etc. shown in the following examples can be changed as appropriate without departing from the gist of the present invention. Accordingly, the scope of the present invention is not limited to the specific examples shown below.

<Semi-aromatic polyamide resin>
(Synthesis of Polyamide (MXD6))
According to the description in paragraph 0038 of JP-A-2011-140620, a semi-aromatic compound obtained by polycondensation of metaxylylenediamine and adipic acid and having a terminal amino group concentration of 40 μeq/g and a terminal carboxyl group concentration of 90 μeq/g A polyamide resin was synthesized. The ratio of terminal amino group concentration to terminal carboxyl group concentration ([NH ₂ ]/[COOH]) was 0.44. The obtained semi-aromatic polyamide resin is called "MXD6".

(Synthesis of Polyamide (MP6-1))
According to the description of Example 2 of Japanese Patent No. 5218705, meta-xylylenediamine, para-xylylenediamine and adipic acid are polycondensed, and the terminal carboxyl group concentration ([COOH]) is 95 μeq/g, the terminal amino group concentration is A semi-aromatic polyamide resin with ([NH ₂ ]) of 45 μeq/g was synthesized ([NH ₂ ]/[COOH]=0.47).

(Synthesis of Polyamide (MP6-2))
Accurately weighed 8768.4 g (60 mol) of adipic acid and sodium hypophosphite monohydrate were placed in a reaction vessel equipped with a stirrer, partial condenser, total condenser, thermometer, dropping funnel, nitrogen inlet tube, and strand die. 3.105 g of compound (NaH ₂ PO ₂ ·H ₂ O) (50 mass ppm as phosphorus atom concentration in polyamide resin) and 1.61 g of sodium acetate were added, and after sufficient nitrogen substitution, nitrogen was added to the internal pressure of 0.4 MPa. After filling, the inside of the system was heated to 170° C. under a small amount of nitrogen stream while stirring. The sodium hypophosphite monohydrate/sodium acetate molar ratio was 0.67.
To this, 8,335 g (61 mol) of a mixed diamine of meta-xylylenediamine and para-xylylenediamine (7:3 (molar ratio)) was added dropwise with stirring. The temperature was raised to After the dropwise addition of the mixed xylylenediamine was completed, the internal temperature was set to 260° C. and the melt polymerization reaction was continued for 20 minutes. Then, the internal pressure was returned to atmospheric pressure at a rate of 0.01 MPa per minute.
Thereafter, the inside of the system was pressurized again with nitrogen, and the polymer was taken out from the strand die and pelletized to obtain about 24 kg of polyamide resin (MP6-2). The obtained pellets were dried with dehumidified air at 80°C (dew point -40°C) for 1 hour. The obtained MP6-2 had a terminal carboxyl group concentration ([COOH]) of 37 μeq/g and a terminal amino group concentration ([NH ₂ ]) of 89 μeq/g.

<Terminal group concentration>
The terminal amino group concentration is measured by dissolving 0.5 g of a semi-aromatic polyamide resin in a mixed solution of 30 mL of phenol/methanol (4:1 by volume) with stirring at 20 to 30° C. and titrating with 0.01N hydrochloric acid. did. As for the terminal carboxyl group concentration, 0.1 g of a semi-aromatic polyamide resin was dissolved in 30 mL of benzyl alcohol at 200°C, and 0.1 mL of phenol red solution was added in the range of 160°C to 165°C. The solution is titrated with a titrant (KOH concentration of 0.01 mol / L) in which 0.132 g of KOH is dissolved in 200 mL of benzyl alcohol, and the color change is yellow to red. It was calculated by taking it as the end point.
The unit of end group concentration is μequivalent/g.

<Fiber>
Glass fiber: ECS03T-296GH manufactured by Nippon Electric Glass Co., Ltd., average fiber length 3.0 mm, short fiber diameter 10.0 μm

<Black colorant>
Carbon black (manufactured by Mitsubishi Chemical Corporation, MA600B)
<Talc>
Micron White #5000S: manufactured by Hayashi Kasei Co., Ltd. <Releasing agent>
Lightamide WH255: manufactured by Kyoeisha Chemical Co., Ltd.

Example 1
Semi-aromatic polyamide resin, talc, release agent and black colorant were weighed and dry-blended so that the final composition would be the composition shown in Table 1 below. TEM26SS) using a twin-screw cassette weighing feeder (CE-W-1-MP, manufactured by Kubota Corporation). As for the black colorant, a part of the semi-aromatic polyamide resin within the range of the amount was used to make a masterbatch and then added. In addition, the glass fiber is fed into the above-mentioned twin-screw extruder from the side of the extruder using a vibrating cassette weighing feeder (CE-V-1B-MP, manufactured by Kubota Corporation), and melted and kneaded with the resin component. , to obtain pellets (polyamide resin composition). The temperature setting of the extruder was 280°C.

<Measurement of water permeability coefficient>
Using the pellets obtained above, using NEX80III-9E manufactured by Nissei Plastic Industry Co., Ltd., a test piece of 100 mm × 100 mm × 1 mm thickness was injection molded at a cylinder temperature of 280 ° C. and a mold surface temperature of 135 ° C.
Next, as shown in FIG. 1, 25 g of calcium chloride particles 12 were placed inside an aluminum cylindrical cup 11 having an inner diameter of 67 mm and an internal height of 80 mm. The test piece 13 was used to seal the cup at a position 50 mm from the inner bottom surface of the cup, and the cup was allowed to stand in an atmosphere of 40° C. and a relative humidity of 90% for 42 hours. The mass of the calcium chloride particles was measured, and the difference (increase) from before standing was taken as the amount of permeated water to calculate the water permeability coefficient.
The unit of moisture permeability coefficient is g·mm/day·m ² .

<Bending strength>
After drying the pellets at 120°C for 4 hours, a 100mm x 100mm x 2mm thickness is molded using a Fanuc injection molding machine (100T) under the conditions of a cylinder temperature of 280°C and a mold surface temperature of 135°C. The product was injection molded. The molding conditions were about 95% filling of the cavity in about 0.5 seconds, and holding pressure was set at about 80% of the VP switching pressure for 10 seconds.
The flexural strength of the molded article obtained was measured according to the ISO-178 standard. The unit of bending strength is MPa.

Example 2
In Example 1, the semi-aromatic polyamide resin was changed to MP6-1, and the rest was carried out in the same manner.

Comparative example 1
In Example 1, the glass fiber was changed to an equal amount of glass flakes (Glass flake REF-015 manufactured by Nippon Sheet Glass Co., Ltd., average thickness 5 μm, average particle size 15 μm), and other operations were performed in the same manner.

Comparative example 2
In Example 2, the semi-aromatic polyamide resin was changed to MP6-2, and the rest was carried out in the same manner.

As is clear from the above results, the molded article of the present invention was excellent in mechanical strength.

11 cup 12 calcium chloride particles 13 test piece

Claims (11)

A semi-aromatic polyamide resin and a fiber having a number average fiber length exceeding 300 μm, wherein the terminal carboxyl group concentration of the semi-aromatic polyamide resin is higher than the terminal amino group concentration, and the difference between the terminal carboxyl group concentration and the terminal amino group concentration is 47 μ equivalent / g or more and less than 100 μ equivalent / g, and the polyamide resin composition is molded to a thickness of 1 mm, 40 ° C., under the conditions of 90% relative humidity A molded product having a moisture permeability coefficient of 3.0 g·mm/day·m ² or less after being left to stand for 42 hours, a number average fiber length of 1.0 mm to 6.0 mm, and being a camera part. . 2. The molded article according to claim 1, which is used for molding a camera part of an on-vehicle camera having a transparent member. The molded article according to claim 1 or 2, wherein said fiber is at least one selected from carbon fiber and glass fiber. The molded article according to any one of claims 1 to 3, wherein the fibers are treated with at least one of a surface treatment agent and a sizing agent. The molded article according to any one of claims 1 to 4, further comprising a black colorant. The molded article according to any one of claims 1 to 5, further comprising talc. Any one of claims 1 to 6, further comprising a black coloring agent and talc, wherein the mass ratio of the black coloring agent to talc (black coloring agent/talc) in the molded product is 1.5 to 2.5. Articles described in paragraph. The molded article according to any one of claims 1 to 7, which is an injection molded article. The molded article according to any one of claims 1 to 8, wherein the camera part has a maximum length of 15 to 40 mm. The molded article according to any one of claims 1 to 9, wherein the camera part contains a member derived from the polyamide resin composition, and the proportion of the member is 1 to 99% by mass. Injection molding a polyamide resin composition comprising a semi-aromatic polyamide resin and fibers having a number average fiber length exceeding 300 μm, wherein the concentration of terminal carboxyl groups of the semi-aromatic polyamide resin is higher than the concentration of terminal amino groups. 11. A method for manufacturing a molded product which is a camera part according to any one of claims 1 to 10.

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