Ester-type resin composition, method for producing said ester-type resin composition, and molded article produced using said ester-type resin
A technology of ester-based resins and compositions, which is applied in the field of ester-based resin compositions, can solve the problems of reduced strength, difficulty in resisting warping, cracking or reduced strength, etc., to prevent a large increase, prevent melt viscosity and solution viscosity, and prevent performance-reducing effect
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[0112] Hereinafter, the present invention will be described in more detail by giving examples and comparative examples, but the present invention is not limited thereto.
[0113] [evaluation items]
[0114] (1) Solution viscosity (intrinsic viscosity) of ester resin composition
[0115] [Polyester resin (PET): Examples 1-9, Comparative Examples 1-4]
[0116] The melt-kneaded polyester resin (PET) was dried at 130° C. for 4 hours, and 0.15 g of the dried resin was dissolved in 30 mL of phenol / tetrachloroethane = 1 / 1, using a Canon Fenske viscometer at 30 °C for measurement. The unit is (dl / g).
[0117] [Polylactic acid resin (PLA): Examples 10, 11, Comparative Examples 5, 6]
[0118] The melt-kneaded polylactic acid resin (PLA) was dried at 110° C. for 4 hours, 0.15 g of the dried resin was dissolved in 30 mL of chloroform, and measured at 30° C. using a Canon Fenske viscometer. The unit is (dl / g).
[0119] (2) Melt viscosity (melt flow resistance) of ester resin
[0120...
Synthetic example 1
[0129] [Synthesis Example 1] Synthesis of Aliphatic Polycarbodiimide
[0130] Add 100 parts by mass of 4,4'-diisocyanate dicyclohexylmethane and 0.5 parts by mass of carbodiimidization catalyst (3-methyl-1-phenyl-2-phosphorus-1-oxide) into the In a reaction vessel with a stirrer, stirring was carried out at 185° C. for 15 hours under a nitrogen flow to obtain poly-4,4′-dicyclohexylmethanecarbodiimide whose terminal is isocyanate.
[0131] Confirmed by infrared absorption (IR) spectroscopy at a wavelength of 2150cm -1 Around the absorption peak of the carbodiimide group. The NCO% was measured to be 4.88% (average degree of polymerization = 6.7).
[0132] Next, heat the poly-4,4'-dicyclohexylmethane carbodiimide obtained above to 120° C., add 40 parts by mass of polyethylene glycol monomethyl ether (average molecular weight: 400) and heat to 150° C. and react under stirring for 5 hours.
[0133] Confirmed by infrared absorption (IR) spectroscopy with a wavelength of 2200-230...
Synthetic example 2
[0134] [Synthesis Example 2] Synthesis of xylene-based polycarbodiimide
[0135] Add 100 parts by mass of m-tetramethylxylylene diisocyanate and 2 parts by mass of carbodiimidization catalyst (3-methyl-1-phenyl-2-phosphorus-1-oxide) into a mixer with a reflux tube and agitator In a reaction vessel, the mixture was stirred at 180° C. for 32 hours under a nitrogen stream to obtain isocyanate-terminated tetramethylxylylenecarbodiimide.
[0136] Confirmed by infrared absorption (IR) spectroscopy at a wavelength of 2150cm -1 Around the absorption peak of the carbodiimide group. The NCO% was measured to be 3.75% (average degree of polymerization = 10.0).
[0137] Next, the polytetramethylphenylenecarbodiimide obtained above isocyanate-terminated was heated to 120°C, 38 parts by mass of polyethylene glycol monomethyl ether (average molecular weight: 500) was added thereto, heated to 150°C and The reaction was carried out under stirring for 6 hours.
[0138] Confirmed by infrared ...
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