JP2022144113A - Polyamide resin composition and polyamide molding - Google Patents

Abstract

To provide a polyamide resin composition which enables deterioration of the flowability thereof to be suppressed, the deterioration occurring when a glass fiber treated with a sizing agent or a surface treatment agent having an acid group is added to the polyamide resin composition.SOLUTION: A polyamide resin composition is provided, including polyamide resin, and a glass fiber including a surface treatment agent or a sizing agent. The surface treatment agent or the sizing agent has an acid group, the polyamide resin is a polyamide resin including a component unit (a) derived from a dicarboxylic acid and a component unit (b) derived from diamine, wherein the component unit (a) derived from the dicarboxylic acid includes a component unit derived from an aromatic dicarboxylic acid or an alicyclic dicarboxylic acid, and the component unit (b) derived from the diamine includes 10 mol% or more and less than 50 mol% of a component unit (b2) derived from 1,3-bis(aminomethyl) cyclohexane with respect to the total number of moles of the component unit (b) derived from the diamine.SELECTED DRAWING: None

Description

TECHNICAL FIELD The present invention relates to a polyamide resin composition and a polyamide molded article.

Conventionally, polyamide resin compositions have been excellent in moldability, mechanical properties and chemical resistance, and are used as materials for various parts such as clothing, industrial materials, automobiles, electrical/electronics and industrial use. widely used as

Various additives are added to the polyamide resin composition used for these applications in order to develop properties suitable for each application. For example, it is known to add a reinforcing material such as glass fiber in order to increase the impact resistance and rigidity of the polyamide resin composition.

The glass fibers may be treated with a sizing agent or a surface treatment agent for the purpose of enhancing dispersibility in the polyamide resin. For example, in Patent Document 1, 20 to 60% by mass of unsaturated dicarboxylic acid or carboxylic acid anhydride, 20 to 75% by mass of methyl acrylate, and 5 to 20% by mass of methyl methacrylate are copolymerized. A glass fiber sizing agent containing a copolymer compound, an aminosilane and a polyurethane resin and having a weight average molecular weight of 10,000 to 60,000 is described. Patent Document 1 describes that the sizing agent can increase the mechanical strength (particularly tensile strength) of a polyamide resin to which glass fibers have been added.

Attempts have also been made to change the raw materials of the polyamide resin to change the physical properties of the polyamide resin. For example, Patent Documents 2 and 3 disclose a polyamide resin using 1,3-bis(aminomethyl)cyclohexane as a diamine component used for producing a polyamide by polycondensing a diamine component and a dicarboxylic acid component. Have been described. Patent Document 2 describes that the polyamide resin described in the document has high transparency, and Patent Document 3 describes that the polyamide resin described in the document has a high glass transition point and a high crystallization ability. stated to be improving.

JP 2014-231452 A JP-A-49-55796 JP 2017-75303 A

The sizing agent described in Cited Document 1 has a carboxyl group derived from an unsaturated dicarboxylic acid or carboxylic acid anhydride. According to the new findings of the present inventors, when glass fibers treated with a sizing agent having a carboxyl group are added to a polyamide resin composition, the fluidity of the polyamide resin composition may decrease. rice field. The above decrease in fluidity was also observed when glass fibers treated with other sizing agents or surface treatment agents having acidic groups were added to the polyamide resin composition.

In view of these circumstances, the present invention provides a polyamide resin composition capable of suppressing a decrease in flowability when adding glass fibers treated with a sizing agent or a surface treatment agent having an acidic group, and the polyamide resin composition. It is an object thereof to provide a polyamide molded article containing

A polyamide resin composition related to one embodiment of the present invention includes a polyamide resin of 20% by mass or more and 80% by mass or less with respect to the total mass of the polyamide resin composition, and 15% by mass or more of the total mass of the polyamide resin composition. and 70% by mass or less of glass fibers containing a surface treatment agent or a sizing agent. The surface treatment agent or sizing agent has an acidic group, and the polyamide resin is a polyamide resin containing a component unit (a) derived from a dicarboxylic acid and a component unit (b) derived from a diamine, The component unit (a) derived from the dicarboxylic acid includes a component unit derived from an aromatic dicarboxylic acid or an alicyclic dicarboxylic acid, and the component unit (b) derived from the diamine is a component unit derived from the diamine. A component unit (b1) derived from an alkylenediamine having 4 to 18 carbon atoms, which is more than 50 mol% and 90 mol% or less relative to the total number of moles of (b), ) and a component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane, which accounts for 10 mol% or more and less than 50 mol% of the total number of moles of ).

A polyamide molded article relating to another embodiment of the present invention includes the polyamide resin composition.

According to the present invention, a polyamide resin composition capable of suppressing a decrease in flowability when glass fibers treated with a sizing agent or a surface treatment agent having an acidic group are added, and polyamide molding containing the polyamide resin composition body can be provided.

1. First Embodiment A first embodiment of the present invention relates to a polyamide resin composition.

The polyamide resin composition is a resin composition in which the main component of the resin component is a polyamide resin. Being the main component means that the polyamide resin accounts for 50% by mass or more of the resin component. The proportion of the polyamide resin in the resin component is preferably 60% by mass or more, more preferably 70% by mass or more, further preferably 80% by mass or more, and 90% by mass or more. is particularly preferred. The upper limit of the proportion of the polyamide resin in the resin component is not particularly limited, but may be 100% by mass or less, may be 90% by mass or less, or may be 80% by mass or less.

The proportion of the polyamide resin contained in the polyamide resin composition is preferably 20% by mass or more and 80% by mass with respect to the total mass of the polyamide resin composition.

1-1. Polyamide resin The polyamide resin may be a polyamide resin containing component units (a) derived from dicarboxylic acid and component units (b) derived from diamine. At this time, in order to set the melting point (Tm) and glass transition temperature (Tg) of the polyamide resin within the above ranges, the component unit (a) derived from a dicarboxylic acid is a component derived from an aromatic dicarboxylic acid or an alicyclic dicarboxylic acid. It is preferable that the component unit (b) derived from diamine has 4 or more carbon atoms and is more than 50 mol% and 90 mol% or less with respect to the total number of moles of component units (b) derived from diamine. 10 mol% or more and less than 50 mol% of 1,3-bis(aminomethyl ) a component unit (b1) derived from cyclohexane.

[Component unit (a) derived from dicarboxylic acid]
When the polyamide resin contains a component unit derived from an aromatic dicarboxylic acid or an alicyclic dicarboxylic acid as the component unit (a) derived from a dicarboxylic acid, the melting point (Tm) and crystallinity can be sufficiently increased.

Examples of aromatic dicarboxylic acids include terephthalic acid, naphthalenedicarboxylic acid and their esters. Examples of cycloaliphatic dicarboxylic acids include cyclohexanedicarboxylic acid and its esters. Among them, from the viewpoint of obtaining a polyamide resin having high crystallinity and high heat resistance, the component unit (a) derived from a dicarboxylic acid preferably contains a component unit derived from an aromatic dicarboxylic acid, and is derived from terephthalic acid. It is more preferable to include a component unit that

The content of component units derived from aromatic dicarboxylic acid or alicyclic dicarboxylic acid (preferably component units derived from aromatic dicarboxylic acid, more preferably component units derived from terephthalic acid) is not particularly limited, but dicarboxylic acid It is preferably 50 mol % or more and 100 mol % or less with respect to the total number of moles of component units (a) derived from an acid. When the content of the component unit is 50 mol % or more, the crystallinity of the polyamide resin can be easily increased. From the same viewpoint, the content of the component unit is more preferably 70 mol % or more and 100 mol % or less.

In the present embodiment, the component unit (a) derived from dicarboxylic acid preferably contains the component unit (a1) derived from terephthalic acid, naphthalenedicarboxylic acid or cyclohexanedicarboxylic acid. These component units (a1) can increase the crystallinity of the polyamide, unlike isophthalic acid, for example. From the viewpoint of ensuring the crystallinity of the polyamide resin, the content of these component units (a1) is more than 20 mol% and 100 mol% or less with respect to the total number of moles of the component units (a) derived from dicarboxylic acid. do. From the viewpoint of further increasing the crystallinity of the polyamide resin, the content of these component units (a1) is 45 mol% or more and 100 mol% or less with respect to the total number of moles of the component units (a) derived from dicarboxylic acid. is preferably 50 mol% or more and 99 mol% or less, more preferably more than 80 mol% and 99 mol% or less, and particularly preferably more than 90 mol% and 99 mol% or less. .

The component unit (a) derived from a dicarboxylic acid is an aromatic carboxylic acid component unit (a2) other than the component unit (a1) or an aliphatic It may contain a dicarboxylic acid component unit (a3). However, from the viewpoint of not impairing the crystallinity of the resin, the content of component units derived from isophthalic acid and component units derived from aliphatic dicarboxylic acids having 4 to 18 carbon atoms other than adipic acid is small. Specifically, it is preferably 20 mol % or less, more preferably 10 mol % or less, relative to the total number of moles of component units (a) derived from dicarboxylic acid.

Examples of aromatic dicarboxylic acid component units (a2) other than terephthalic acid include component units derived from isophthalic acid and 2-methylterephthalic acid. Among these, component units derived from isophthalic acid are preferred. From the viewpoint of ensuring the crystallinity of the polyamide resin, the content of these component units (a2) is 1 mol% or more and 50 mol% or less with respect to the total number of moles of the component units (a) derived from dicarboxylic acid. is preferably 1 mol % or more and 20 mol % or less, more preferably 1 mol % or more and 10 mol % or less, and particularly preferably 1 mol % or more and 5 mol % or less.

The component unit (a3) derived from an aliphatic dicarboxylic acid is a component unit derived from an aliphatic dicarboxylic acid having an alkylene group having 4 to 20 carbon atoms, and has an alkylene group having 6 to 12 carbon atoms. A structural unit derived from an aliphatic dicarboxylic acid is preferred. Examples of the above aliphatic dicarboxylic acids include malonic acid, dimethylmalonic acid, succinic acid, glutaric acid, adipic acid, 2-methyladipic acid, trimethyladipic acid, pimelic acid, 2,2-dimethylglutaric acid, 3,3 - includes diethylsuccinic acid, azelaic acid, sebacic acid, suberic acid component units, etc. Among these, adipic acid and sebacic acid are preferred. From the viewpoint of ensuring the crystallinity of the polyamide resin, the content of these component units (a3) is 0 mol% or more and 40 mol% or less with respect to the total number of moles of the component units (a) derived from dicarboxylic acid. more preferably 0 mol % or more and 20 mol % or less, more preferably 1 mol % or more and 10 mol % or less, and particularly preferably 1 mol % or more and 5 mol % or less.

The semi-aromatic polyamide resin (A) contains, in addition to the component units (a1), (a2), and (a3) described above, a small amount of a tribasic or higher tribasic compound such as trimellitic acid or pyromellitic acid. may further contain a polyvalent carboxylic acid component unit. The content of such polyvalent carboxylic acid component units can be 0 mol % or more and 5 mol % or less with respect to the total number of moles of component units (a) derived from dicarboxylic acids.

[Component unit (b) derived from diamine]
A polyamide resin, in addition to a component unit (b1) derived from an alkylenediamine having 4 to 18 carbon atoms as a component unit (b) derived from a diamine, is derived from 1,3-bis(aminomethyl)cyclohexane. When the component unit (b2) is included, the glass transition temperature (Tg) can be sufficiently increased.

That is, since the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane has a nonlinear structure, it reduces the mobility of the molecular chains of the polyamide resin. Therefore, the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane has the glass transition temperature (Tg) of the polyamide resin having the component unit (b2). can be higher than polyamide resins that do not have In addition, it is believed that this allows the polyamide resin having the component unit (b2) to have high mechanical strength even in a high-temperature, high-humidity environment, and to maintain this high mechanical strength for a long period of time.

Furthermore, the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane has the melting point (Tm) of the polyamide resin having the component unit (b2), and does not have the component unit (b2). It can be lowered more moderately than polyamide resin. As a result, the polyamide resin having the component unit (b2) has high fluidity during injection molding and high moldability.

By the way, according to the findings of the present inventors, the decrease in fluidity when adding glass fibers treated with a sizing agent having an acidic group or a surface treatment agent is due to the presence of the sizing agent in the melted area of the polyester resin composition. Alternatively, it is considered that the acid group of the surface treatment agent reacts with the amino terminal of the polyester resin. In other words, the reaction causes the polyester resin and the glass fiber to bond together via the sizing agent or the surface treatment agent, increasing the apparent molecular weight of the polyester resin. It is believed that the increase in the apparent molecular weight reduces the fluidity of the polyester resin composition. On the other hand, the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane bends the molecular chain of the polyester resin to cause moderate steric hindrance, and the sizing agent or surface treatment agent has It inhibits the reaction between acid groups and amino termini of polyester resins. It is believed that this suppresses an increase in the apparent molecular weight of the polyester resin and suppresses a decrease in fluidity of the polyester resin composition when a sizing agent or surface treatment agent having an acidic group is used.

In addition, the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane bends the molecular chain of the polyester resin and suppresses penetration of water into the interior of the polyester resin composition. As a result, the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane makes the polyester resin difficult to hydrolyze. It is believed that this suppresses the decrease in the mechanical strength (especially tensile strength) of the molded article of the polyester resin composition, particularly in a high-temperature and high-humidity environment.

In addition, since the above polyamide resin has crystallinity due to the component unit (b1) derived from alkylenediamine having 4 to 18 carbon atoms, it has high fluidity and mechanical strength during injection molding. Furthermore, since the polyamide resin has a high glass transition temperature (Tg), it has high mechanical strength even in a high temperature range, and it is believed that these high mechanical strengths are likely to be maintained.

The number of carbon atoms in the alkylenediamine having 4 or more and 18 or less carbon atoms, which is the raw material of the component unit (b1), is more preferably 4 or more and 10 or less from the viewpoint of making the Tg of the resin less likely to decrease.

The alkylenediamine having 4 to 18 carbon atoms may include linear alkylenediamine or branched alkylenediamine. From the viewpoint of enhancing the crystallinity of the resin, the alkylenediamine having 4 to 18 carbon atoms preferably includes linear alkylenediamine. That is, component units derived from alkylenediamines having 4 to 18 carbon atoms preferably include component units derived from straight-chain alkylenediamines.

Examples of alkylenediamines having 4 to 18 carbon atoms include 1,4-diaminobutane, 1,6-diaminohexane, 1,7-diaminoheptane, 1,8-octanediamine, 1,9-nonanediamine, and Included are linear alkylenediamines such as 1,10-decanediamine, 2-methyl-1,5-pentanediamine, and branched alkylenediamines such as 2-methyl-1,8-octanediamine. . Among these, 1,4-diaminobutane, 1,6-diaminohexane, 1,9-nonanediamine, 1,10-decanediamine, 2-methyl-1,5-pentanediamine, and 2-methyl-1,8 -octanediamine is preferred, 1,6-diaminohexane and 1,10-decanediamine are preferred. One of these alkylenediamines may be used, or two or more of them may be used.

The content of component units (b1) derived from alkylenediamines having 4 to 18 carbon atoms is more than 50 mol% and 90 mol% or less with respect to the total number of moles of component units (b) derived from diamines. is preferred. When the content is more than 50 mol %, the crystallinity of the polyamide resin can be sufficiently enhanced, and the fluidity and mechanical strength of the resin during injection molding can be enhanced. When the content is 90 mol % or less, the content of the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane can be increased. As a result, the glass transition temperature (Tg) of the polyamide resin can be increased to increase the mechanical strength in a high temperature range, and the (Tm) of the polyamide resin can be moderately decreased to improve moldability.

On the other hand, the content of component units (b2) derived from 1,3-bis(aminomethyl)cyclohexane is 10 mol% or more and less than 50 mol% with respect to the total number of moles of component units (b) derived from diamine. is preferably When the content is 10 mol% or less, the glass transition temperature (Tg) of the polyamide resin is increased, the mechanical strength in a high temperature range is increased, and the (Tm) of the polyamide resin is moderately decreased, resulting in moldability. can increase When the content is less than 50 mol %, the content of the component unit (b1) derived from an alkylenediamine having 4 to 18 carbon atoms can be increased. As a result, the crystallinity of the polyamide resin can be sufficiently improved to further increase the mechanical strength of the molded product, and the polyamide resin itself by the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane. A decrease in fluidity can be suppressed.

From the above viewpoint, the content of the component unit (b1) derived from an alkylenediamine having 4 to 18 carbon atoms is more than 50 mol% and 90 mol with respect to the total number of moles of the component unit (b) derived from a diamine. % or less, more preferably 55 mol % or more and 85 mol % or less, and even more preferably 60 mol % or more and 80 mol % or less.

In addition, from the above viewpoint, the content of the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane is 10 mol% or more with respect to the total number of moles of the component unit (b) derived from diamine. It is preferably less than mol%, more preferably 15 mol% or more and less than 45 mol%, further preferably 20 mol% or more and 40 mol% or less, and 20 mol% or more and 38 mol% or less. is more preferable, and 20 mol % or more and 33 mol % or less is particularly preferable.

The component unit (b) derived from a diamine may further contain a component unit (b3) derived from another diamine as long as the effect of the present invention is not impaired. Examples of other diamines include aromatic diamines and cycloaliphatic diamines. The content of component units (b3) derived from other diamines may be 50 mol% or less with respect to the total number of moles of component units (b) derived from diamines.

At least part of the molecular terminal groups of the polyamide resin may be blocked with a terminal blocking agent from the viewpoint of increasing thermal stability during compounding or molding and further increasing mechanical strength. The terminal blocking agent is preferably a monoamine when the molecular terminal is a carboxyl group, and is preferably a monocarboxylic acid when the molecular terminal is an amino group.

Examples of monoamines include aliphatic monoamines such as methylamine, ethylamine, propylamine, and butylamine, cycloaliphatic monoamines such as cyclohexylamine and dicyclohexylamine, and aromatic monoamines such as aniline and toluidine. is included. Examples of monocarboxylic acids include acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, caprylic acid, lauric acid, tridecylic acid, myristic acid, palmitic acid, stearic acid, oleic acid and linoleic acid. aliphatic monocarboxylic acids having 2 to 30 atoms, aromatic monocarboxylic acids including benzoic acid, toluic acid, naphthalenecarboxylic acid, methylnaphthalenecarboxylic acid and phenylacetic acid; and alicyclic monocarboxylic acids including cyclohexanecarboxylic acid and the like. Contains carboxylic acids. Aromatic monocarboxylic acids and alicyclic monocarboxylic acids may have a substituent on the cyclic structure portion.

[Physical properties]
The polyamide resin can have a melting point (Tm) measured by a differential scanning calorimeter (DSC) of 280° C. or higher and 330° C. or lower, and a glass transition temperature (Tg) measured by DSC of 135° C. or higher and 180° C. °C or less.

When the melting point (Tm) of the polyamide resin is 280 ° C. or higher, the mechanical strength and heat resistance of the polyamide resin composition and the molded article are unlikely to be impaired in a high temperature range, and when it is 330 ° C. or lower, the molding temperature is excessively increased. Since there is no need to increase the viscosity, the moldability of the polyamide resin composition tends to be good. From the above viewpoint, the melting point (Tm) of the polyamide resin is more preferably 290° C. or higher and 330° C. or lower, and further preferably 300° C. or higher and 330° C. or lower.

When the glass transition temperature (Tg) of the polyamide resin is 135° C. or higher, the heat resistance of the polyamide resin composition and the molded article is less likely to be impaired, and at the same time the mechanical strength in a high temperature range can be increased. When the glass transition temperature (Tg) of the polyamide resin is 180°C or lower, the polyamide resin composition tends to have good moldability. From the above viewpoint, the glass transition temperature (Tg) of the polyamide resin is more preferably 140°C or higher and 170°C or lower.

The heat of fusion (ΔH) of the polyamide resin is preferably 10 mJ/mg or more. When the heat of fusion (ΔH) of the polyamide resin is 10 mJ/mg or more, the polyamide resin has crystallinity, so that fluidity and mechanical strength during injection molding can be easily increased. From the same viewpoint, the heat of fusion (ΔH) of the polyamide resin is more preferably 15 mJ/mg or more, further preferably 20 mJ/mg or more. Although the upper limit of the heat of fusion (ΔH) of the polyamide resin is not particularly limited, it can be 90 mJ/mg from the viewpoint of not impairing moldability.

The heat of fusion (ΔH), melting point (Tm) and glass transition temperature (Tg) of the polyamide resin can be measured using a differential scanning calorimeter (DSC220C, manufactured by Seiko Instruments Inc.).

Specifically, about 5 mg of polyamide resin is sealed in an aluminum pan for measurement and heated from room temperature to 350°C at 10°C/min. Hold at 360° C. for 3 minutes to completely melt the resin, then cool to 30° C. at 10° C./min. After 5 minutes at 30°C, heat a second time to 360°C at 10°C/min. The endothermic peak temperature (° C.) in this second heating is taken as the melting point (Tm) of the crystalline polyamide resin, and the displacement point corresponding to the glass transition is taken as the glass transition temperature (Tg). The heat of fusion (ΔH) is determined according to JIS K7122 from the area of the endothermic peak of crystallization during the first heating process.

The melting point (Tm), glass transition temperature (Tg) and heat of fusion (ΔH) of the polyamide resin are the structure of the component unit (a) derived from the dicarboxylic acid, the component unit derived from the diamine represented by the formula (1) The content of (b2), the content ratio of the component unit (b1) derived from the alkylenediamine having 4 to 18 carbon atoms and the component unit (b2) derived from the diamine represented by the formula (1), and the number of carbon atoms It can be adjusted by adjusting the number of carbon atoms in the alkylenediamine, which is 4 or more and 18 or less.

Further, when the heat of fusion (ΔH) of the polyamide resin is increased, the content and content ratio of the component unit (b2) (the ratio of the component unit (b2) to the total number of moles of the component unit (b) derived from diamine) should be low. On the other hand, when the glass transition temperature (Tg) of the polyamide resin is increased and the melting point (Tm) is decreased, for example, the content or content ratio of the component unit (b2) (total moles of component units (b) derived from diamine The ratio of component units (b2) to the number) is preferably high.

The intrinsic viscosity [η] of the polyamide resin measured in 96.5% sulfuric acid at a temperature of 25° C. is preferably 0.6 dl/g or more and 1.5 dl/g or less. When the intrinsic viscosity [η] of the polyamide resin is 0.6 dl/g or more, the mechanical strength (toughness, etc.) of the molded body can be sufficiently increased, and when it is 1.5 dl/g or less, the resin composition Fluidity during molding is less likely to be impaired. From the same viewpoint, the intrinsic viscosity [η] of the polyamide resin is more preferably 0.8 dl/g or more and 1.2 dl/g or less. The intrinsic viscosity [η] can be adjusted by the terminal capping amount of the polyamide resin.

The intrinsic viscosity of the polyamide resin can be measured according to JIS K6810-1977.
Specifically, 0.5 g of the above polyamide resin is dissolved in 50 ml of a 96.5% sulfuric acid solution to prepare a sample solution. The number of seconds the sample solution flows down can be measured using an Ubbelohde viscometer under the condition of 25±0.05° C., and the obtained value can be applied to the following formula for calculation.
[η]=ηSP/[C(1+0.205ηSP)]

In the above formula, each algebra or variable represents:
[η]: Intrinsic viscosity (dl/g)
ηSP: specific viscosity C: sample concentration (g/dl)

ηSP is obtained by the following formula.
ηSP=(t−t0)/t0
t: number of seconds for the sample solution to flow down (seconds)
t0: Number of seconds for blank sulfuric acid to flow down (seconds)

The terminal amino group content of the polyamide resin is preferably 10 mmol/kg or more and 150 mmol/kg or less, more preferably 15 mmol/kg or more and 130 mmol/kg or less, and 20 mmol/kg or more and 100 mmol/kg or less. is more preferred. If the amount of terminal amino groups of the polyamide resin is 150 mmol/kg or more, the fluidity tends to decrease when glass fibers treated with a surface treatment agent or a sizing agent having an acidic group are added, so the above polyamide resin is used. The effect of suppressing the decrease in fluidity due to use is remarkable. When the terminal amino group content of the polyamide resin is 150 mmol/kg or less, the fluidity of the resin composition can be sufficiently ensured.

The terminal amino group content is a value measured by the following method. 1 g of polyamide resin is dissolved in 35 mL of phenol, mixed with 2 mL of methanol, and used as a sample solution. Using thymol blue as an indicator, the sample solution is titrated with a 0.01N HCl aqueous solution to determine the amount of terminal amino groups ([NH ₂ ], unit: mmol/kg).

[Production method]
The polyamide resin can be produced, for example, by polycondensing the aforementioned dicarboxylic acid and the aforementioned diamine in a uniform solution. Specifically, a dicarboxylic acid and a diamine are heated in the presence of a catalyst as described in WO 03/085029 to obtain a lower condensate, and then the lower condensate is It can be produced by subjecting a melt to polycondensation by applying shear stress.

From the viewpoint of adjusting the intrinsic viscosity of the polyamide resin, etc., the aforementioned end blocking agent may be added to the reaction system. The intrinsic viscosity [η] (or molecular weight) of the polyamide resin can be adjusted by the amount of the terminal blocker added.

A terminal blocking agent is added to the reaction system of the dicarboxylic acid and the diamine. The amount added is preferably 0.07 mol or less, more preferably 0.05 mol or less, per 1 mol of the total amount of dicarboxylic acid.

1-2. Glass fiber The polyamide fiber includes glass fiber.

The type of the glass fiber is not particularly limited as long as it is used for reinforcing the resin, and may be chopped strand or milled fiber having a shorter fiber length. The cross-sectional shape of the glass fiber may be circular or non-circular such as elliptical or oval.

The average fiber length of the glass fiber can be, for example, 1 μm or more and 20 mm or less, preferably 5 μm or more and 10 mm or less, from the viewpoint of improving the moldability of the resin composition and improving the mechanical strength and heat resistance of the resulting molded product. Further, the aspect ratio of the glass fiber can be, for example, 5 or more and 2000 or less, preferably 30 or more and 600 or less.

The average fiber length and average fiber diameter of glass fibers can be measured by the following methods.
1) After dissolving the resin composition in a hexafluoroisopropanol/chloroform solution (0.1/0.9% by volume), the solution is filtered and collected.
2) The filtrate obtained in 1) above is dispersed in water, and the fiber length (Li) and fiber diameter (di) of each of 300 arbitrary fibers are measured with an optical microscope (magnification: 50 times). Let qi be the number of fibers whose fiber length is Li, and calculate the weight average length (Lw) based on the following equation, and use this as the average fiber length of the glass fibers.
Weight average length (Lw)=(Σqi×Li ² )/(Σqi×Li)
Similarly, the number of fibers having a fiber diameter of Di is defined as ri, and the weight average diameter (Dw) is calculated based on the following formula, and is defined as the average fiber diameter of the glass fibers.
Weight average diameter (Dw)=(Σri×Di ² )/(Σri×Di)

The content of the glass fiber is not particularly limited, but can be, for example, 15% by mass or more and 70% by mass or less, and is 15% by mass or more and 50% by mass or less with respect to the total mass of the polyamide resin composition. is preferred, and more preferably 20% by mass or more and 50% by mass or less.

The glass fibers contain a surface treatment agent or a sizing agent.

The surface treating agent or sizing agent may be any known surface treating agent or sizing agent used for glass fibers blended in the polyamide resin composition. However, the surface treatment agent or sizing agent has an acidic group. Examples of the acidic groups include carboxy groups, anhydride groups, ester groups and sulfonic acid groups. Among these, a carboxy group, an acid anhydride group and an ester group are preferred, and a carboxy group and an acid anhydride group are more preferred. The ester group may be a functional group derived from a carboxylic acid ester.

Examples of surface treatment agents having acidic groups include silane coupling agents containing acid anhydride groups such as 3-trimethoxysilylpropylsuccinic anhydride.

Examples of sizing agents having acidic groups include sizing agents comprising homopolymers or copolymers of unsaturated carboxylic acids, or copolymers of unsaturated carboxylic acids or their anhydrides with unsaturated monomers. .

Examples of the unsaturated carboxylic acids include acrylic acid, methacrylic acid, cinnamic acid, itaconic acid, fumaric acid, mesaconic acid, citraconic acid and maleic acid. Examples of anhydrides of the above unsaturated carboxylic acids include maleic anhydride, itaconic anhydride, dodecenylsuccinic anhydride, and the like. Of these, acrylic acid, methacrylic acid, maleic acid and maleic anhydride are preferred.

Examples of such unsaturated monomers include styrene, butadiene, acrylonitrile, vinyl acetate, methyl acrylate, ethyl acrylate, methyl methacrylate, ethyl methacrylate, methylstyrene, ethylene, propylene, butylene, isobutylene, vinyl ethers, and the like. be Of these, methyl acrylate and methyl methacrylate are preferred, and it is more preferred to include both methyl acrylate and methyl methacrylate.

When the sizing agent contains a copolymer of the unsaturated carboxylic acid or its anhydride and an unsaturated monomer, the ratio of the unsaturated carboxylic acid or its anhydride to the total mass of the copolymer is 20% by mass or more. It is preferably 60% by mass or less. When the above proportion is 20% by mass or more, the effect of improving the mechanical strength of the polyamide resin composition by increasing the chemical interaction with the polyamide resin by the acidic group (carboxy group) is remarkable. When the above ratio is 60% by mass or less, the effect of improving the mechanical strength of the polyamide resin composition by increasing the molecular weight (chain length) of the copolymer and enhancing the physical interaction with the polyamide resin is obtained. Remarkable.

The above homopolymers or copolymers may be used in combination with other resins such as urethane resins and epoxy resins.

(Production method)
The glass fiber containing the surface treatment agent or sizing agent is applied (applied) to the fiber strand using a known method such as a roller applicator during the manufacturing process of the glass fiber. It can be obtained by drying and reacting.

The amount of the surface treatment agent or sizing agent attached to 100 parts by mass of glass fiber is preferably 0.2 parts by mass or more and 3 parts by mass or less, and 0.2 parts by mass or more and 2 parts by mass. It is more preferably 0.3 parts by mass or more and 2 parts by mass or less. When the adhesion amount is 0.2 parts by mass or more, the bundling property of the glass fibers is further improved. Moreover, the thermal stability of a resin composition improves more that the said adhesion amount is 2 mass parts or less.

1-3. Other Components The polyamide resin composition may contain other known components.

Examples of other ingredients include reinforcing materials other than glass fiber, crystal nucleating agents, lubricants, flame retardants, corrosion resistance improvers, anti-drip agents, ion scavengers, elastomers (rubber), antistatic agents, and release agents. , antioxidants (phenols, amines, sulfur and phosphorus, etc.), heat stabilizers (lactone compounds, vitamin E, hydroquinones, copper halides and iodine compounds, etc.), light stabilizers (benzotriazoles, triazines, benzophenones, benzoates, hindered amines and oxanilides, etc.), other polymers (polyolefins, olefin copolymers such as ethylene/propylene copolymers, ethylene/1-butene copolymers, propylene/1 -olefin copolymers such as butene copolymers, polystyrene, polyamides, polycarbonates, polyacetals, polysulfones, polyphenylene oxides, fluororesins, silicone resins and LCPs). Above all, the resin composition of the present invention preferably further contains a reinforcing material from the viewpoint of increasing the mechanical strength of the molded article.

Examples of reinforcing materials other than glass fibers include fibrous reinforcing materials such as wollastonite, potassium titanate whiskers, calcium carbonate whiskers, aluminum borate whiskers, magnesium sulfate whiskers, zinc oxide whiskers, milled fibers and cut fibers, as well as particulate reinforcements.

A crystal nucleating agent can increase the crystallinity of a molded body. Examples of nucleating agents include 2,2-methylenebis(4,6-di-t-butylphenyl)sodium phosphate, tris(pt-butylbenzoate)aluminum, and metals such as stearates. Salt compounds, sorbitol compounds including bis(p-methylbenzylidene)sorbitol and bis(4-ethylbenzylidene)sorbitol, and inorganic substances including talc, calcium carbonate, hydrotalcite, and the like are included. Among these, talc is preferable from the viewpoint of increasing the degree of crystallinity of the molded product. One type of these crystal nucleating agents may be used alone, or two or more types may be used in combination.

The content of the crystal nucleating agent is preferably 0.1 parts by mass or more and 5 parts by mass or less, more preferably 0.1 parts by mass or more and 3 parts by mass or less, relative to the total mass of the polyamide resin composition. preferable. When the content of the crystal nucleating agent is within the above range, the degree of crystallinity of the molded body can be sufficiently increased, and sufficient mechanical strength can be easily obtained.

A lubricant enhances the injection fluidity of the polyamide resin composition and improves the appearance of the obtained molded article. Lubricants can be fatty acid metal salts such as oxycarboxylic acid metal salts and higher fatty acid metal salts.

The oxycarboxylic acid constituting the oxycarboxylic acid metal salt may be either an aliphatic oxycarboxylic acid or an aromatic oxycarboxylic acid. Examples of the above aliphatic oxycarboxylic acids include α-hydroxymyristic acid, α-hydroxypalmitic acid, α-hydroxystearic acid, α-hydroxyeicosanoic acid, α-hydroxydocosanoic acid, α-hydroxytetraeicosanoic acid. , α-hydroxyhexaeicosanoic acid, α-hydroxyoctaeicosanoic acid, α-hydroxytriacontanoic acid, β-hydroxymyristic acid, 10-hydroxydecanoic acid, 15-hydroxypentadecanic acid, 16-hydroxyhexadecanoic acid, 12- Aliphatic oxycarboxylic acids having 10 to 30 carbon atoms such as hydroxystearic acid and ricinoleic acid are included. Examples of the aromatic oxycarboxylic acids include salicylic acid, m-oxybenzoic acid, p-oxybenzoic acid, gallic acid, mandelic acid, and trobaic acid.

Examples of metals constituting the metal oxycarboxylate include alkali metals such as lithium and alkaline earth metals such as magnesium, calcium and barium.

Among these, the metal oxycarboxylic acid salt is preferably a metal salt of 12-hydroxystearate, more preferably magnesium 12-hydroxystearate and calcium 12-hydroxystearate.

Examples of the higher fatty acid constituting the higher fatty acid metal salt include higher fatty acids having 15 to 30 carbon atoms such as stearic acid, oleic acid, behenic acid, behenic acid and montanic acid.

Examples of metals constituting the higher fatty acid metal salt include calcium, magnesium, barium, lithium, aluminum, zinc, sodium and potassium.

Among these, the higher fatty acid metal salt is preferably calcium stearate, magnesium stearate, barium stearate, calcium behenate, sodium montanate, calcium montanate, or the like.

The content of the lubricant is preferably 0.01% by mass or more and 1.3% by mass or less with respect to the total mass of the polyamide resin composition. When the content of the lubricant is 0.01% by mass or more, the fluidity during molding tends to increase, and the appearance of the obtained molded article tends to improve. When the content of the lubricant is 1.3% by mass or less, the decomposition of the lubricant is less likely to generate gas during molding, and the appearance of the product tends to be good.

1-4. Production method The polyamide resin composition is prepared by mixing the above-described polyamide resin and, if necessary, other components with a known resin kneading method, such as a Henschel mixer, a V blender, a ribbon blender, or a tumbler blender, or by mixing After that, it is further melt-kneaded with a single-screw extruder, a multi-screw extruder, a kneader, or a Banbury mixer, and then granulated or pulverized.

2. Applications of Resin Composition The resin composition of the present invention is used as various polyamide molded articles by molding by known molding methods such as compression molding, injection molding, and extrusion molding.

The molded article of the resin composition of the present invention can be used for various purposes. Examples of such applications include automotive applications such as radiator grilles, rear spoilers, wheel covers, wheel caps, cowl vent grilles, air outlet louvers, air scoops, hood bulges, sunroofs, sunroof rails, fenders and back doors. Exterior parts, cylinder head covers, engine mounts, air intake manifolds, throttle bodies, air intake pipes, radiator tanks, radiator supports, water pumps, water pump inlets, water pump outlets, thermostat housings, cooling fans, fans Automotive engine compartment parts such as shrouds, oil pans, oil filter housings, oil filler caps, oil level gauges, oil pumps, timing belts, timing belt covers and engine covers, fuel caps, fuel filler Automotive fuel system components such as tubes, automotive fuel tanks, fuel sender modules, fuel cut-off valves, quick connectors, canisters, fuel delivery pipes and fuel filler necks, automotive such as shift lever housings and propeller shafts Automotive chassis parts such as drive system parts, stabilizer bars/linkage rods, engine mount brackets, window regulators, door locks, door handles, outside door mirror stays, wipers and their parts, accelerator pedals, pedal modules, joints Automotive functional parts such as resin screws, nuts, bushes, seal rings, bearings, bearing retainers, gears and actuators, wire harness connectors, relay blocks, sensor housings, fuse parts, encapsulation, ignition coils and distributors・Electronic parts for automobiles such as caps, fuel system parts for general-purpose equipment such as fuel tanks for general-purpose equipment (brush cutters, lawn mowers and chain saws), electric and electronic parts such as connectors and LED reflectors, building material parts, industrial equipment Parts, various housings or exterior parts such as small housings (including housings for personal computers, mobile phones, etc.), exterior molded products, etc. are included.

Above all, the resin composition of the present invention is suitable for use in high-temperature and high-humidity environments, such as in-vehicle members, especially tubes through which antifreeze flows, because the mechanical strength is less reduced even in high-temperature and high-humidity environments. In addition, the resin composition of the present invention can be suitably used for parts of electric equipment such as electronic parts for automobiles, electrical and electronic parts, industrial equipment parts, and housings or exterior parts of electric equipment.

In the following, the invention is illustrated with reference to examples. The examples should not be construed as limiting the scope of the present invention.

In the experiments below, the melting point (Tm), glass transition temperature (Tg), intrinsic viscosity, heat of fusion, and terminal amino group content of the polyamide resin were measured by the following methods.

(Melting point (Tm), glass transition temperature (Tg))
The heat of fusion (ΔH), melting point (Tm) and glass transition temperature (Tg) of the polyamide resin were measured using a differential scanning calorimeter (DSC220C, manufactured by Seiko Instruments Inc.).

Specifically, about 5 mg of polyamide resin was sealed in an aluminum pan for measurement and heated from room temperature to 350°C at 10°C/min. It was held at 360°C for 3 minutes to completely melt the resin, then cooled to 30°C at 10°C/min. After 5 minutes at 30°C, it was heated a second time to 360°C at 10°C/min. The endothermic peak temperature (°C) in this second heating was taken as the melting point (Tm) of the crystalline polyamide resin, and the displacement point corresponding to the glass transition was taken as the glass transition temperature (Tg). The heat of fusion (ΔH) was obtained from the area of the endothermic peak of crystallization during the first heating process according to JIS K7122.

(Intrinsic viscosity [η])
The intrinsic viscosity [η] of the polyamide resin is obtained by dissolving 0.5 g of the polyamide resin in 50 ml of a 96.5% sulfuric acid solution, and the number of seconds the resulting solution flows down under the conditions of 25 ° C. ± 0.05 ° C. It was measured using an Ubbelohde viscometer and calculated based on the formula: [η]=ηSP/(C(1+0.205ηSP)).
[η]: Intrinsic viscosity (dl/g)
ηSP: specific viscosity C: sample concentration (g/dl)
t: number of seconds for the sample solution to flow down (seconds)
t0: Number of seconds for blank sulfuric acid to flow down (seconds)
ηSP=(t−t0)/t0

(heat of fusion (ΔH))
The heat of fusion (ΔH) of the polyamide resin was determined according to JIS K 7122 (2012) from the area of the exothermic peak of crystallization during the first heating process.

(Amount of terminal amino group)
1 g of polyamide resin was dissolved in 35 mL of phenol and mixed with 2 mL of methanol to prepare a sample solution. Using thymol blue as an indicator, the sample solution was titrated with a 0.01N HCl aqueous solution to determine the amount of terminal amino groups ([NH ₂ ], unit: mmol/kg).

1. Synthesis/preparation of materials 1-1. Synthesis of Polyamide Resin (Synthesis Example 1)
259.5 g (1561.7 mmol) of terephthalic acid, 128.1 g (1102.0 mmol) of 1,6-diaminohexane, 67.2 g (472.3 mmol) of 1,3-bis(aminomethyl)cyclohexane, sodium hypochlorite 0.37 g of sodium phosphate monohydrate and 81.8 g of distilled water were placed in a 1 L autoclave and purged with nitrogen. Stirring was started from 190° C., and the internal temperature was raised to 250° C. over 3 hours. At this time, the internal pressure of the autoclave was increased to 3.0 MPa. After the reaction was continued for 1 hour, the autoclave was vented to the atmosphere through a spray nozzle installed at the bottom of the autoclave to extract low order condensates. Then, after cooling this low-order condensate to room temperature, the low-order condensate was pulverized with a pulverizer to a particle size of 1.5 mm or less and dried at 110° C. for 24 hours.

Next, this low-order condensate was placed in a tray-type solid phase polymerization apparatus, and after purging with nitrogen, the temperature was raised to 215° C. over about 1 hour and 30 minutes. After that, the reaction was allowed to proceed for 1 hour and 30 minutes, and the temperature was lowered to room temperature.

Thereafter, the obtained prepolymer is melt-polymerized in a twin-screw extruder with a screw diameter of 30 mm and L/D = 36 at a barrel setting temperature of 330°C, a screw rotation speed of 200 rpm, and a resin feed rate of 6 kg/h. , to obtain a polyamide resin 1.

The resulting polyamide resin 1 had an intrinsic viscosity [η] of 0.9 dl/g, a melting point (Tm) of 323°C, a glass transition temperature (Tg) of 154°C, a heat of fusion (ΔH) of 51 mJ/mg, and terminal amino groups. was 23 mmol/kg.

(Synthesis example 2)
Synthesis except that the amount of 1,6-diaminohexane put in the autoclave was 118.9 g (1023.1 mmol) and the amount of 1,3-bis(aminomethyl)cyclohexane was 78.4 g (551.1 mmol) Polyamide resin 2 was obtained in the same manner as in Example 1. The intrinsic viscosity [η] of polyamide resin 2 is 0.9 dl / g, the melting point (Tm) is 320 ° C., the glass transition temperature (Tg) is 156 ° C., the heat of fusion (ΔH) is 48 mJ / mg, and the amount of terminal amino groups is 25 mmol/kg.

(Synthesis Example 3)
Synthesis except that the amount of 1,6-diaminohexane put in the autoclave was 109.9 g (944.5 mmol) and the amount of 1,3-bis(aminomethyl)cyclohexane was 89.5 g (629.7 mmol) Polyamide resin 3 was obtained in the same manner as in Example 1. The intrinsic viscosity [η] of polyamide resin 3 is 0.9 dl / g, the melting point (Tm) is 305 ° C., the glass transition temperature (Tg) is 166 ° C., the heat of fusion (ΔH) is 35 mJ / mg, and the amount of terminal amino groups is 25 mmol/kg.

(Synthesis Example 4)
The amount of 1,6-hexanediamine put into the autoclave was 280 g (2410 mmol), the amount of terephthalic acid was 277.4 g (1670 mmol), the amount of isophthalic acid was 119.6 g (720 mmol), and the amount of benzoic acid was 3. Polyamide resin 4 was obtained in the same manner as in Synthesis Example 1 except that 0.66 g (30 mmol) was added, the amount of sodium hypophosphite monohydrate was changed to 5.7 g, and the amount of distilled water was changed to 545 g. Polyamide resin 4 has an intrinsic viscosity of 1.0 dl/g, a melting point (Tm) of 330° C., a glass transition temperature (Tg) of 125° C., a heat of fusion (ΔH) of 50 J/g, and an amount of terminal amino groups of 25 mmol/kg. Met.

1-2. Glass fiber ・Glass fiber surface-modified by acid modification (manufactured by Owens Corning: FT-2A)

1-3. Lubricant sodium montanate (manufactured by Clariant, LICOMONT NAV101 "LICOMONT" is a registered trademark of the company)

1-4. Crystal nucleating agent Talc

2. Preparation of polyamide resin composition The above materials are mixed in a tumbler blender at the composition ratio (unit: parts by mass) shown in Table 1, and the cylinder temperature is 300 to 335 ° C. using a 30 mmφ vented twin screw extruder. It was melt-kneaded under the following conditions. After that, the kneaded product was extruded into strands and cooled in a water bath. After that, the strand was collected by a pelletizer and cut to obtain a polyamide resin composition in the form of pellets.

3. Evaluation The obtained polyamide resin composition was evaluated according to the following criteria.

3-1. Flow length Each polyamide resin composition was injected under the following conditions using a bar flow mold with a width of 10 mm and a thickness of 0.5 mm, and the flow length (mm) of the polyamide resin composition in the mold was measured. . It should be noted that the longer the flow length, the better the injection fluidity.
Molding machine: EC75N-2A manufactured by Toshiba Machine Co., Ltd.
Injection set pressure: 2000 kg/cm ²
Molding machine cylinder temperature: 335°C
Mold temperature: 160°C

3-2. Flow length maintenance rate before and after blending of glass fiber The above flow length of the polyamide resin composition blended with glass fiber and the polyamide resin composition in which the blending amount of the additive was the same amount except that the glass fiber was not blended The flow length was compared with the above flow length, and the maintenance rate of the flow length before and after blending the glass fiber was calculated.

3-3. Tensile strength (initial)
Each polyamide resin composition was injection molded under the following conditions to prepare an ASTM-1 (dumbbell piece) test piece having a thickness of 3.2 mm.
Molding machine: SE50DU manufactured by Sumitomo Heavy Industries, Ltd.
Molding machine cylinder temperature: Melting point of polyamide resin +10°C
Mold temperature: Polyamide resin glass transition temperature +20°C
The prepared test piece was allowed to stand at a temperature of 23° C. in a nitrogen atmosphere for 24 hours according to ASTM D638. Then, according to ASTM D638, a tensile test was performed under an atmosphere of 23° C. and 50% relative humidity to measure the tensile strength.

3-4. Tensile strength (after high humidity treatment)
The test piece was left for 500 hours under conditions of 121° C. temperature, 2 atmospheric pressure, and 100% RH. Thereafter, the test piece was allowed to cool to 23° C., and a tensile test was performed in accordance with ASTM D638 at a temperature of 23° C. and a relative humidity of 50% to measure the tensile strength.

3-5. Retention Rate of Tensile Strength By comparing the initial tensile strength and the tensile strength after the high-humidity treatment, the ratio (retention rate) of the tensile strength after the high-humidity treatment to the initial tensile strength was calculated.

Table 1 shows the composition, flow length, flow length retention, tensile strength (initial), tensile strength (after high-humidity treatment), and tensile strength retention of the prepared polyamide resin composition.

As is clear from Table 1, the polyamide resin having the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane is a surface treatment agent having an acidic group or a glass fiber containing a sizing agent. It is possible to suppress the decline in sexuality. In addition, the polyamide resin having the component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane can suppress a decrease in mechanical strength in a high-temperature/high-humidity environment.

According to the polyamide resin composition of the present invention, it is possible to achieve both improvement in mechanical strength and suppression of decrease in fluidity by adding glass fibers treated with a sizing agent or surface treatment agent having an acidic group. can. Therefore, the present invention is expected to expand the applicability of polyamide resins to various uses and contribute to the further spread of polyamide resins.

Claims (9)

A polyamide resin of 20% by mass or more and 80% by mass or less with respect to the total mass of the polyamide resin composition;
15% by mass or more and 70% by mass or less of glass fibers containing a surface treatment agent or a sizing agent with respect to the total mass of the polyamide resin composition,
The surface treatment agent or sizing agent has an acidic group,
The polyamide resin is
A polyamide resin containing a component unit (a) derived from a dicarboxylic acid and a component unit (b) derived from a diamine,
The component unit (a) derived from the dicarboxylic acid includes a component unit derived from an aromatic dicarboxylic acid or an alicyclic dicarboxylic acid,
The component unit (b) derived from the diamine is
A component unit (b1) derived from an alkylenediamine having 4 to 18 carbon atoms, which is more than 50 mol% and 90 mol% or less with respect to the total number of moles of the component units (b) derived from the diamine;
A component unit (b2) derived from 1,3-bis(aminomethyl)cyclohexane, which accounts for 10 mol% or more and less than 50 mol% of the total number of moles of the component units (b) derived from the diamine;
including,
Polyamide resin composition. 2. The polyamide resin composition according to claim 1, wherein said acidic group possessed by said surface treatment agent or sizing agent is a carboxy group, an acid anhydride group, or an ester group. The polyamide resin is 15 mol% or more and less than 45 mol% of the total number of moles of the component units (b) derived from the diamine, and the component units (b2) derived from 1,3-bis(aminomethyl)cyclohexane. The polyamide resin composition according to claim 1 or 2, comprising: The component unit (b1) derived from an alkylenediamine having 4 to 18 carbon atoms includes a component unit derived from a linear alkylenediamine or a branched alkylenediamine.
The polyamide resin composition according to any one of claims 1 to 3. The linear alkylenediamine or branched alkylenediamine includes 1,4-diaminobutane, 1,6-diaminohexane, 1,9-nonanediamine, 1,10-decanediamine, 2-methyl-1,5 - a diamine selected from the group consisting of pentanediamine and 2-methyl-1,8-octanediamine;
The polyamide resin composition according to claim 4. The aromatic dicarboxylic acid or alicyclic dicarboxylic acid is terephthalic acid, naphthalenedicarboxylic acid or cyclohexanedicarboxylic acid,
The polyamide resin composition according to any one of claims 1 to 5. The polyamide resin composition according to any one of claims 1 to 6, which is a resin composition for in-vehicle members. Containing the polyamide resin composition according to any one of claims 1 to 7,
Polyamide molding. It is an in-vehicle component,
The polyamide molded article according to claim 8.