Preparation method and application of a fully biodegradable resin with excellent hydrolysis resistance
A technology of degrading resin and whole biology is applied in the field of preparation of whole biodegradable resin, which can solve the problems of easy hydrolysis and difficult to meet the requirements of crop growth cycle in the service cycle.
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[0026] The invention provides a kind of preparation method of full biodegradable resin, comprises the following steps:
[0027] mixing terephthalic acid, 1,4-butanediol and a nucleating agent to perform an esterification and dehydration reaction to obtain a first intermediate product system;
[0028] Mixing the first intermediate product system with adipic acid, performing a second esterification and dehydration to obtain a second intermediate product system;
[0029] mixing the second intermediate product system, a catalyst and a stabilizer, and performing a polycondensation reaction to obtain a fully biodegradable resin;
[0030] The full biodegradable resin is PBAT.
[0031] In the present invention, unless otherwise specified, all raw material components are commercially available products well known to those skilled in the art.
[0032] The invention mixes terephthalic acid, 1,4-butanediol and a nucleating agent to carry out esterification and dehydration reaction to ob...
Embodiment 1
[0051] Mix 1kg of terephthalic acid and 3kg of 1,4-butanediol, heat to 200°C, stir evenly, mix with 20g of nucleating agent (β-cyclodextrin), and carry out negative pressure esterification dehydration at 180°C Reaction for 3 hours (at this time, the water yield reached 87% of the theoretical value, and the value of the esterified carboxyl group was 598mol / t), and the first intermediate product system was obtained;
[0052] The first intermediate product system is mixed with 1 kg of adipic acid under stirring conditions, and the negative pressure esterification dehydration reaction is carried out at 240 ° C for 2 hours (at this time, the water output reaches 90% of the theoretical value, and the esterified carboxyl value is 420mol / t), obtain the second intermediate product system;
[0053] The second intermediate product system, 30g catalyst (tetraethyl titanate and tetraisopropyl titanate compounded according to the mass ratio of 4:1) and 30g stabilizer (dibutyl phosphite and...
Embodiment 2
[0055] Mix 1kg terephthalic acid and 3kg 1,4-butanediol, heat to 200°C, stir evenly, mix with 30g nucleating agent (β-cyclodextrin), and carry out negative pressure esterification dehydration at 180°C React for 3 hours (at this time, the water yield reaches 85% of the theoretical value, and the esterified carboxyl value is 623mol / t), and the first intermediate product system is obtained;
[0056] The first intermediate product system was mixed with 1 kg of adipic acid under stirring conditions, and a negative pressure esterification dehydration reaction was carried out at 240° C. for 2 hours (at this time, the water yield reached 91% of the theoretical value, and the value of the esterified carboxyl group was 412mol / t), obtain the second intermediate product system;
[0057] The second intermediate product system 30g catalyst (tetraethyl titanate and tetraisopropyl titanate compounded according to the mass ratio of 4:1) and 30g stabilizer (dibutyl phosphite and dibutyl phospha...
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