JP2012102257A - Resin-based part excellent in chlorofluocarbons barrier property - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a resin-based part excellent in a chlorofluocarbons barrier property in the resin-based part to be used for enclosing chlorofluocarbons.SOLUTION: The resin-based part excellent in the chlorofluocarbons barrier property, used for enclosing the chlorofluocarbons, includes a polyamide (A) obtained by carrying out polycondensation of: a diamine component containing at least 30 mol% of 1,3-bis(aminomethyl)cyclohexane; and a dicarboxylic acid component.

Description

  The present invention relates to a resin part having excellent barrier properties for chlorofluorocarbons used for enclosing chlorofluorocarbons.

As refrigerants for air conditioners and refrigerators, so-called chlorofluorocarbons such as chlorofluorocarbon, fluorocarbon, hydrochlorofluorocarbon, hydrofluorocarbon and the like have been known. 1,1,2-tetrafluoroethane (HFC134a) is used. However, although the ozone depletion coefficient of HFC134a is 0, the global warming coefficient is 1300 (when CO ₂ is 1), and if released into the atmosphere, it causes global warming, which is not preferable.
Metal is mainly used as a component for encapsulating refrigerants for air conditioners and refrigerators. However, for the purpose of weight reduction, it is possible to use thermoplastic resin instead of metal, or to make plastic parts to prevent destruction of vibration parts. The use of hoses is being considered. However, a general resin component member is inferior in barrier properties against chlorofluorocarbons, and chlorofluorocarbons are released into the atmosphere. In order to prevent the emission, it is necessary to increase the thickness of the material.
Regarding such a chlorofluorocarbon barrier property, Patent Document 1 or 2 discloses a hose that is strong in chlorofluorocarbon gas barrier properties, but the methods disclosed in these documents did not provide sufficient chlorofluorocarbon barrier properties. Moreover, the strength when it was made into resin parts other than a hose was not enough.

JP-A-6-294484 JP-A-6-294485

  An object of the present invention is to solve the above-mentioned problems and to provide a resin part that is used for enclosing chlorofluorocarbons and has excellent chlorofluorocarbon barrier properties.

  As a result of intensive studies, the inventors of the present invention contain a polyamide (A) obtained by polycondensation of a diamine component containing 30 mol% or more of 1,3-bis (aminomethyl) cyclohexane and a dicarboxylic acid component. It has been found that the above-mentioned problems can be solved by a resin part having an excellent barrier property for chlorofluorocarbons used for enclosing chlorofluorocarbons.

  The resin part of the present invention is a resin part used for enclosing chlorofluorocarbons, and has excellent chlorofluorocarbon barrier properties, and can be used as a hose, tube, film, connector, joint, etc. Target value is high.

  The resin part of the present invention is a resin part used for enclosing chlorofluorocarbons, and is obtained by polycondensing a diamine component containing 30 mol% or more of 1,3-bis (aminomethyl) cyclohexane and a dicarboxylic acid component. It is a resin part containing the polyamide (A) obtained in this way and having excellent chlorofluorocarbon barrier properties.

  The polyamide (A) used in the present invention has good chlorofluorocarbon barrier properties and good chlorofluorocarbon barrier properties under high humidity. Examples of the polyamide (A) include polyamides obtained by polycondensation of a diamine component mainly composed of 1,3-bis (aminomethyl) cyclohexane and various dicarboxylic acid components. From the viewpoint that the polyamide (A) has good fluorocarbon barrier properties, 1,3-bis (aminomethyl) cyclohexane is 30 mol% or more, preferably 50 mol% or more, more preferably 70 mol% or more, More preferably, it is obtained using a diamine component containing 80 mol% or more, particularly preferably 90 mol% or more. This polyamide (A) may be a homopolymer or a copolymer. The polyamide (A) has high fluorocarbon barrier performance, and has good heat resistance and molding processability. The polyamide (A) may be a single type of resin, but a plurality of resins may be blended and used.

  The 1,3-bis (aminomethyl) cyclohexane used as the diamine component in the present invention includes a cis isomer and a trans isomer. By controlling the cis / trans ratio, the melting point and glass transition point of the polyamide (A) can be arbitrarily controlled. From this viewpoint, the cis / trans ratio is preferably 50/50 to 100/0. More preferably, it is 60 / 40-100 / 0, More preferably, it is 70 / 30-100 / 0. By setting it as this range, melting | fusing point becomes 200 degreeC or more, heat resistance becomes favorable, and polyamide has crystallinity. Moreover, it is preferable from the viewpoint that the fluorocarbon barrier property is improved.

Examples of diamine components other than 1,3-bis (aminomethyl) cyclohexane that can be used in the production of polyamide (A) include tetramethylenediamine, pentamethylenediamine, 2-methylpentanediamine, hexamethylenediamine, heptamethylenediamine, and octamethylene. Aliphatic diamines such as diamine, nonamethylenediamine, decamethylenediamine, dodecamethylenediamine, 2,2,4-trimethyl-hexamethylenediamine, 2,4,4-trimethylhexamethylenediamine; 1,4-bis (aminomethyl) ) Cyclohexane, 1,3-diaminocyclohexane, 1,4-diaminocyclohexane, bis (4-aminocyclohexyl) methane, 2,2-bis (4-aminocyclohexyl) propane, bis (aminomethyl) decalin, bis ( Alicyclic diamines such as minomethyl) tricyclodecane; diamines having an aromatic ring such as bis (4-aminophenyl) ether, paraphenylenediamine, metaxylylenediamine, paraxylylenediamine, bis (aminomethyl) naphthalene, etc. However, the present invention is not limited to these examples.
In the present invention, among diamine components other than the 1,3-bis (aminomethyl) cyclohexane, 1,4-bis (aminomethyl) cyclohexane is preferably used from the viewpoint of improving heat resistance.

  Examples of the dicarboxylic acid component that can be used for producing the polyamide (A) include aliphatic dicarboxylic acids such as succinic acid, glutaric acid, pimelic acid, suberic acid, azelaic acid, adipic acid, sebacic acid, undecanedioic acid, and dodecanedioic acid. An aromatic dicarboxylic acid such as terephthalic acid, isophthalic acid or 2,6-naphthalenedicarboxylic acid can be exemplified, but is not limited thereto. Among the above dicarboxylic acid components, in the present invention, from the viewpoint of good moldability and controlling the melting point within a preferable range, α, ω-linear aliphatic having 4 to 20 carbon atoms such as adipic acid and sebacic acid. Dicarboxylic acid, isophthalic acid and the like are preferably used.

  In the present invention, in addition to the diamine component and the dicarboxylic acid component, as a component constituting the polyamide (A), lactams such as ε-caprolactam and laurolactam, aminocaproic acid, and aminoundecane are used as long as the effects of the present invention are not impaired. Aliphatic aminocarboxylic acids such as acids can also be used as copolymerization components.

  Examples of the polyamide (A) that can be used in the present invention include polyamides composed of 1,3-bis (aminomethyl) cyclohexane and isophthalic acid, polyamides composed of 1,3-bis (aminomethyl) cyclohexane, caprolactam, and isophthalic acid. It can be illustrated.

  As a polyamide (A) that can be preferably used in the present invention in view of the effects of the present invention, a diamine component containing 1,3-bis (aminomethyl) cyclohexane and an α, ω-linear aliphatic dicarboxylic acid having 4 to 20 carbon atoms Examples thereof include polyamides obtained by polycondensation with a dicarboxylic acid component mainly composed of an acid. Examples of the α, ω-linear aliphatic dicarboxylic acid having 4 to 20 carbon atoms include succinic acid, glutaric acid, pimelic acid, suberic acid, azelaic acid, adipic acid, sebacic acid, undecanedioic acid, and dodecanedioic acid. Aliphatic dicarboxylic acids such as acids can be exemplified, but among these, adipic acid and sebacic acid are preferable.

  As the polyamide (A) that can be preferably used in the present invention in terms of the effects of the present invention, 1,3-bis (aminomethyl) cyclohexane is 30 mol% or more, preferably 50 mol% or more, more preferably 70 mol% or more, More preferably 80 mol% or more, particularly preferably 90 mol% or more of the diamine component and C4-20 α, ω-linear aliphatic dicarboxylic acid is preferably 50 mol% or more, more preferably 70 mol%. As mentioned above, polyamides obtained by polycondensation with a dicarboxylic acid component containing 80 mol% or more, particularly preferably 90 mol% or more can be exemplified.

As such a polyamide, a polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane and adipic acid, and a polycondensation of 1,3-bis (aminomethyl) cyclohexane and sebacic acid are obtained. Preferred examples include polyamide, polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane, adipic acid and sebacic acid.
By using adipic acid and sebacic acid in combination as a dicarboxylic acid component, heat resistance, gas barrier properties, and crystallinity can be arbitrarily controlled. When it is desired to lower the crystallinity or when it is in an amorphous state, the sebacic acid / adipic acid ratio (molar ratio) is preferably 80/20 to 30/70, more preferably 70/30 to 40/60. When importance is attached to gas barrier properties, the sebacic acid / adipic acid ratio (molar ratio) is preferably 50/50 or less, more preferably 40/60 or less, and even more preferably 30/70 or less. When importance is attached to heat resistance, the sebacic acid / adipic acid ratio (molar ratio) is preferably 60/40 or less, more preferably 40/60 or less, and even more preferably 30/70 or less.

  Moreover, as polyamide (A) which can be preferably used in the present invention, polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane and adipic acid, 1,3-bis (aminomethyl) cyclohexane and sebacine Examples thereof include a polyamide mixture obtained by polycondensation with an acid. Mixing a polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane and adipic acid and a polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane and sebacic acid Thus, it is possible to arbitrarily control heat resistance and gas barrier properties while maintaining crystallinity. When emphasizing gas barrier properties, polycondensation of polyamide / 1,3-bis (aminomethyl) cyclohexane and adipic acid obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane and sebacic acid The obtained polyamide ratio (mass ratio) is preferably 50/50 or less, more preferably 40/60 or less, and even more preferably 30/70 or less.

The method for producing the polyamide (A) is not particularly limited except that the above-described raw material components are used, and it is produced by appropriately selecting conventionally known methods and polymerization conditions. For example, by a method in which a nylon salt composed of 1,3-bis (aminomethyl) cyclohexane and adipic acid is heated in a pressurized state in the presence of water and polymerized in a molten state while removing added water and condensed water. Manufactured. It can also be produced by a method in which 1,3-bis (aminomethyl) cyclohexane is directly added to molten adipic acid and polycondensed under normal pressure. In this case, in order to keep the reaction system in a uniform liquid state, 1,3-bis (aminomethyl) cyclohexane is continuously added to adipic acid, during which the reaction temperature does not fall below the melting point of the generated oligoamide and polyamide. Thus, polycondensation proceeds while the reaction system is heated.
A small amount of monoamine or monocarboxylic acid may be added as a molecular weight regulator during the polycondensation of the polyamide. The polyamide (A) may be subjected to solid phase polymerization after being produced by a melt polymerization method.

  The number average molecular weight (Mn) of the polyamide (A) is preferably from 18000 to 70000, more preferably from 20000 to 50000, as a PMMA (polymethyl methacrylate) conversion value by GPC (gel permeation chromatography) measurement. Within this range, the heat resistance and moldability are good.

  The melting point or softening point of the polyamide (A) is preferably from 100 to 280 ° C, more preferably from 120 to 270 ° C. Within this range, melting in the extruder is facilitated, and productivity and moldability are improved.

  The glass transition point (Tg) of the polyamide (A) is preferably 80 to 120 ° C, more preferably 100 to 110 ° C. Within this range, the heat resistance is good.

  The melting point and glass transition point can be measured by DSC (Differential Scanning Calorimetry) method. The measurement can be performed, for example, by using DSC-50 manufactured by Shimadzu Corporation, heating the sample from about room temperature to 300 ° C. under the condition of a temperature increase rate of 10 ° C./min with a sample amount of about 5 mg. The atmosphere gas is nitrogen at 30 ml / min. A so-called midpoint temperature (Tgm) was adopted as the glass transition point. As is widely known, Tgm is the midpoint temperature of the intersection of the tangent line of the baseline and the transition slope of the glass state and the supercooled state (rubber state) in the DSC curve.

  The flexural modulus of the polyamide (A) is preferably 2.5 to 5.0 GPa, more preferably 2.6 to 4.5 GPa, and still more preferably 2.7 to 4.4 GPa. Within this range, the strength is good when a resin part is formed. In addition, a bending elastic modulus can measure what heat-processed the injection molded piece of thickness 4mm at 150 degreeC for 1 hour based on JISK7171.

  A phosphorous compound can be added to the polyamide (A) in order to increase the processing stability during melt molding or to prevent the polyamide (A) from being colored. As the phosphorus compound, a phosphorus compound containing an alkali metal or an alkaline earth metal is preferably used. For example, an alkali metal or alkaline earth metal phosphate such as sodium, magnesium, calcium, hypophosphite, phosphorus Acid salts may be mentioned, but those using alkali metal or alkaline earth metal hypophosphites are particularly preferred because they are particularly excellent in the anti-coloring effect of polyamide. Content of a phosphorus compound is 1-500 ppm as a phosphorus atom in polyamide (A), Preferably it is 1-350 ppm, More preferably, it is 1-200 ppm.

The resin component of the present invention has an HFC-134a (1,1,1,2-tetrafluoroethane) permeability coefficient of 1 cc · mm / m ² · day for polyamide (A) at a temperature of 80 ° C. and a relative humidity of 0% RH. · Atm or less, preferably 0.8 cc · mm / m ² · day · atm or less, more preferably 0.5 cc · mm / m ² · day · atm or less. Within this range, barrier properties against chlorofluorocarbons are good.
Examples of the chlorofluorocarbons in the chlorofluorocarbon barrier property include those used as refrigerants for air conditioners and refrigerators, and examples include chlorofluorocarbons, fluorocarbons, hydrochlorofluorocarbons, hydrofluorocarbons, and the like.

  It is preferable to mix | blend the carbodiimide compound (C) with the resin-made components of this invention. Resin parts with excellent chlorofluorocarbon barrier properties are parts such as air conditioners and refrigerators for automobiles, etc., but these parts are susceptible to physical shocks such as vibration, and are particularly hot and humid in the case of automobiles. Because it is used in a rough environment, the resin tends to deteriorate. When the resin is deteriorated, there are problems that the member is destroyed or the fluorocarbon barrier properties are deteriorated. However, by adding the carbodiimide compound (C) to the polyamide (A) of the present invention, the terminal carboxyl group or the amino group of the polyamide (A) reacts with the carbodiimide compound (C), and the molecular chain of the polyamide (A). By extending the length, it is possible to improve the deterioration resistance when used in a high-temperature and high-humidity environment, etc., and it is possible to prevent the destruction of members and to suppress the deterioration of the fluorocarbon barrier properties.

  Preferred examples of the carbodiimide compound (C) include aromatic, aliphatic or alicyclic polycarbodiimide compounds produced by various methods. Among these, an aliphatic or alicyclic polycarbodiimide compound is preferable, and an alicyclic polycarbodiimide compound is more preferably used from the viewpoint of melt kneadability at the time of extrusion or the like. As specific products, Nisshinbo Chemical Co., Ltd. Carbodilite LA-1, Rhein Chemie Co. Stabaxol P and Stabaxol P-400 can be preferably used. These products are preferable because of their high reactivity with the polyamide (A) and high effect in improving the deterioration resistance.

  These carbodiimide compounds (C) can be produced by decarboxylation condensation reaction of organic polyisocyanate. For example, a method of synthesizing various organic polyisocyanates by decarboxylation condensation reaction at a temperature of about 70 ° C. or higher in an inert solvent or without using a solvent in the presence of a carbodiimidization catalyst can be exemplified. . The isocyanate group content is preferably 0.1 to 5%, more preferably 1 to 3%. By setting it as the above range, reaction with polyamide (A) becomes easy and it exists in the tendency for hydrolysis resistance to become favorable.

As organic polyisocyanate which is a synthesis raw material of the carbodiimide compound (C), for example, various organic diisocyanates such as aromatic diisocyanate, aliphatic diisocyanate, and alicyclic diisocyanate, and mixtures thereof can be used.
Specific examples of the organic diisocyanate include 1,5-naphthalene diisocyanate, 4,4′-diphenylmethane diisocyanate, 4,4′-diphenyldimethylmethane diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, 2 , 4-tolylene diisocyanate, 2,6-tolylene diisocyanate, hexamethylene diisocyanate, cyclohexane-1,4-diisocyanate, xylylene diisocyanate, isophorone diisocyanate, dicyclohexylmethane-4,4-diisocyanate, methylcyclohexane diisocyanate, tetramethylxylylene Range isocyanate, 2,6-diisopropylphenyl isocyanate, 1,3,5-triisopropylbenzene-2,4-di Isocyanate, methylenebis (4,1-cyclohexylene) = can be exemplified diisocyanate may be used in combination of two or more thereof. Among these, dicyclohexylmethane-4,4-diisocyanate and methylenebis (4,1-cyclohexylene) = diisocyanate are preferable.

  In order to seal the terminal of the carbodiimide compound (C) and control the degree of polymerization, it is also preferable to use a terminal blocking agent such as monoisocyanate. Examples of the monoisocyanate include phenyl isocyanate, tolyl isocyanate, dimethylphenyl isocyanate, cyclohexyl isocyanate, butyl isocyanate, and naphthyl isocyanate, and two or more kinds may be used in combination.

  In addition, as terminal blocker, it is not limited to said monoisocyanate, What is necessary is just an active hydrogen compound which can react with isocyanate. Examples of such active hydrogen compounds include aliphatic, aromatic, and alicyclic compounds such as methanol, ethanol, phenol, cyclohexanol, N-methylethanolamine, polyethylene glycol monomethyl ether, and polypropylene glycol monomethyl ether. -OH group compounds, secondary amines such as diethylamine and dicyclohexylamine, primary amines such as butylamine and cyclohexylamine, carboxylic acids such as succinic acid, benzoic acid and cyclohexanecarboxylic acid, ethyl mercaptan, allyl mercaptan, thiophenol, etc. Examples of these compounds include thiols and compounds having an epoxy group, and two or more of them may be used in combination.

  Examples of the carbodiimidization catalyst include 1-phenyl-2-phospholene-1-oxide, 3-methyl-1-phenyl-2-phospholene-1-oxide, 1-ethyl-2-phospholene-1-oxide, 3- Metal catalysts such as methyl-2-phospholene-1-oxide and phospholene oxides such as these 3-phospholene isomers, tetrabutyl titanate, etc. can be used. -Methyl-1-phenyl-2-phospholene-1-oxide is preferred. Two or more carbodiimidization catalysts may be used in combination.

  The content of the carbodiimide compound (C) is preferably 0.1 to 2 parts by mass, more preferably 0.1 to 1.5 parts by mass, and still more preferably 0 to 100 parts by mass of the polyamide (A). .2 to 1.5 parts by mass, particularly preferably 0.3 to 1.5 parts by mass. If the amount is less than 0.1 parts by mass, the resin composition does not have sufficient hydrolysis resistance, uneven discharge during melt kneading such as extrusion tends to occur, and melt kneading tends to be insufficient. On the other hand, when it exceeds 2 parts by mass, the viscosity of the resin composition during melt kneading is remarkably increased, and melt kneadability and moldability are liable to deteriorate.

The end group concentration of the polyamide (A) is preferably in the following range in order to increase the reactivity with the carbodiimide compound (C).
The polyamide (A) preferably has a terminal amino group concentration of less than 100 μequivalent / g, more preferably 5 to 75 μequivalent / g, still more preferably 10 to 50 μequivalent / g, and a terminal carboxyl group concentration of preferably 100 μequivalent / g. Less than, more preferably 10 to 90 μeq / g, and still more preferably 10 to 50 μeq / g. By setting the terminal amino group concentration and the terminal carboxyl group concentration within the above ranges, the reaction with the carbodiimide compound (C) is facilitated and the deterioration resistance tends to be good.

  The resin part of the present invention may contain an inorganic filler. By using the inorganic filler, it is possible to improve the rigidity, dimensional stability, workability, etc. of the part.

  In addition, the resin parts of the present invention have a matting agent, a weather stabilizer, an ultraviolet absorber, a nucleating agent, a plasticizer, a flame retardant, an antistatic agent, an anti-coloring agent, as long as the effects of the present invention are not impaired. Additives such as an antigelling agent, a colorant, and a release agent can be added.

  Furthermore, the resin component of the present invention can be blended with one or more resins such as polyamide, polyester, polyolefin, polyphenylene sulfide, and polycarbonate other than the polyamide (A) within a range not impairing the object of the present invention.

  Especially, since polyamide other than polyamide (A) can be blended preferably and the mechanical physical property of a molded article can be improved, aliphatic polyamide resin can be blended more preferably. As the aliphatic polyamide resin, nylon 6, nylon 66, nylon 11, nylon 12, nylon 46, nylon 610, nylon 612, nylon 666, or the like can be used alone or in combination.

  The resin part of the present invention is a part used for enclosing chlorofluorocarbons, specifically, a part for enclosing a refrigerant such as an air conditioner or a refrigerator, for example, a hose, a tube, a film, a connector, a joint. , Gaskets, packing, seal parts and the like. These can be formed by a known method, and are particularly useful as a hose, piping connector or joint.

  The resin part of the present invention can be reduced in thickness because the fluorocarbon barrier properties are greatly improved. In the present invention, as the thickness of the resin part, for example, in the case of a hose, a tube, a film or the like, the thickness of the layer made of polyamide (A) can be 1000 μm or less, preferably 50 to 800 μm. can do. Moreover, in the case of a connector, a joint, etc., it can be 0.1-5 mm, Preferably it can be 0.2-3 mm. Of course, use of other thicknesses is not excluded.

  EXAMPLES Hereinafter, although an Example and a comparative example demonstrate this invention further more concretely, this invention is not limited to these Examples. In this example, various measurements were performed by the following methods.

(1) Fluorocarbon barrier properties Under the atmosphere of 80 ° C. and 0% RH, the fluorocarbon permeability of the film is determined according to the JIS K7126-1: 2006 differential pressure method, and the fluorocarbon permeability coefficient (cc · mm / m ² · day). In addition, HFC-134a (1,1,1,2-tetrafluoroethane) was used as chlorofluorocarbons. In addition, it shows that fluorocarbon barrier property is so favorable that the value of fluorocarbon transmission coefficient is low.

(2) Melting point of polyamide, glass transition point It was determined by differential scanning calorimetry (DSC) using DSC-60 manufactured by Shimadzu Corporation. As measurement conditions, a sample of about 5 mg was heated at a temperature of 10 ° C./min, rapidly cooled when it reached 300 ° C., and heated again at a temperature of 10 ° C./min.

(3) Number average molecular weight The PMMA conversion value was calculated | required by GPC measurement using the Tosoh company make HLC-8320GPC. In addition, TSKgel SuperHM-H was used for the measurement column, hexafluoroisopropanol (HFIP) in which sodium trifluoroacetate was dissolved at 10 mmol / l was used as the solvent, and the measurement temperature was 40 ° C. A calibration curve was prepared by dissolving 6 levels of PMMA in HFIP.

<Production Example 1>
(Synthesis of polyamide (A1))
Adipic acid (manufactured by Rhodia) was heated and melted at 170 ° C. in a reaction vessel, and 1,3-bis (aminomethyl) cyclohexane (manufactured by Mitsubishi Gas Chemical Co., Ltd.) was then added to adipic acid while stirring the contents. The temperature was raised to 240 ° C. while gradually dropping so that the molar ratio of to was 1: 1. After completion of dropping, the temperature was raised to 260 ° C. After completion of the reaction, the contents were taken out in a strand shape and pelletized with a pelletizer. The obtained pellets were charged into a tumbler and subjected to solid phase polymerization under reduced pressure to obtain a polyamide (A1) having a molecular weight adjusted. As 1,3-bis (aminomethyl) cyclohexane, a cis / trans ratio adjusted to 74/26 was used. Polyamide (A1) had a melting point of 230 ° C., a glass transition point of 103 ° C., and a number average molecular weight of 30000.

<Production Example 2>
(Synthesis of polyamide (A2))
A polyamide (A2) was synthesized in the same manner as in Production Example 1 except that sebacic acid (TA Grade manufactured by Ito Oil Co., Ltd.) was used instead of adipic acid. Polyamide (A2) had a melting point of 181 ° C., a glass transition point of 84 ° C., and a number average molecular weight of 30000.

<Production Example 3>
(Synthesis of polyamide (A3))
A polyamide (A3) was synthesized in the same manner as in Production Example 1 except that a mixed dicarboxylic acid having a molar ratio of sebacic acid to adipic acid of 4: 6 was used instead of sebacic acid. Polyamide (A3) had a melting point of 135 ° C., a glass transition point of 98 ° C., and a number average molecular weight of 35,000.

<Production Example 4>
The polyamides (A1) and (A2) produced in Production Example 1 and Production Example 2 were dry blended in a tumbler at a weight ratio of 1: 1 to obtain a mixed polyamide.

<Example 1>
Polyamide (A1) was extruded using a twin screw extruder equipped with a 30 mmφ screw and a T die to obtain a 50 μm thick film. The evaluation results are shown in Table 1.

<Examples 2 to 4>
A film was obtained in the same manner as in Example 1 except that the polyamide (A) was as described in Table 1. The evaluation results are shown in Table 1.

<Example 5>
A film was obtained in the same manner as in Example 1 by dry blending 95.5% by mass of polyamide (A1) and 0.5% by mass of Nisshinbo Chemical's Carbodilite LA-1. The evaluation results are shown in Table 1. Moreover, although the obtained film was boiled at 100 ° C. for 24 hours, the mechanical properties of the film were not deteriorated and the barrier property was the same as that before the treatment.

The abbreviations listed in Table 1 are as follows.
A1: Polyamide (A1) obtained in Production Example 1
A2: Polyamide obtained in Production Example 2 (A2)
A3: Polyamide obtained in Production Example 3 (A3)

  As shown in the above examples, the resin-made part of the present invention is excellent in fluorocarbon barrier properties and has high industrial value.

Claims (11)

  Fluorocarbon barrier properties used to encapsulate chlorofluorocarbons containing polyamide (A) obtained by polycondensation of a diamine component containing 30 mol% or more of 1,3-bis (aminomethyl) cyclohexane and a dicarboxylic acid component Excellent plastic parts.   The resin part according to claim 1, wherein the polyamide (A) has a glass transition point Tg of 80 to 120 ° C. The polyamide (A) has a 1,1,1,2-tetrafluoroethane (HFC-134a) permeability coefficient at 80 ° C. and 0% RH of 1 cc · mm / m ² · day · atm or less. The resin parts described.   The dicarboxylic acid in which the polyamide (A) contains a diamine component containing 30 mol% or more of 1,3-bis (aminomethyl) cyclohexane and 50 mol% or more of an α, ω-linear aliphatic dicarboxylic acid having 4 to 20 carbon atoms. The resin part according to any one of claims 1 to 3, which is a polyamide obtained by polycondensation of components.   The resin part according to any one of claims 1 to 3, wherein the polyamide (A) is a polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane and adipic acid.   The resin part according to any one of claims 1 to 3, wherein the polyamide (A) is a polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane and sebacic acid.   The resin part according to any one of claims 1 to 3, wherein the polyamide (A) is a polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane, adipic acid and sebacic acid.   Polyamide (A) is obtained by polycondensation of polyamide obtained by polycondensation of 1,3-bis (aminomethyl) cyclohexane and adipic acid, 1,3-bis (aminomethyl) cyclohexane and sebacic acid. The resin part according to any one of claims 1 to 3, which is a polyamide mixture.   The resin-made part in any one of Claims 1-8 which contain 0.1-2 mass parts of carbodiimide compounds (C) with respect to 100 mass parts of polyamides (A).   The resin part according to claim 9, wherein the carbodiimide compound (C) is an aliphatic or alicyclic polycarbodiimide compound.   The resin part according to any one of claims 1 to 10, selected from a hose, a tube, a film, a connector, a joint, a gasket, a packing, and a seal part.