Water-soluble copolyester and preparation method thereof
A copolyester, water-soluble technology, used in textiles, papermaking, fiber processing, etc., can solve the problems of affecting production efficiency, fabric quality, poor hairiness attached to the slurry, and increased yarn breakage. Good adhesion to hairiness, reducing the effect of broken ends
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[0029] Example 1
[0030] 14.6kg of terephthalic acid, 6.6kg of isophthalic acid, 9.5kg of dimethyl isophthalate-5-sodium sulfonate, 15.8kg of ethylene glycol and 2.5kg of caprolactone were put into the 100L stainless steel reactor, And add 28g of zinc acetate, 28g of trifluoromethanesulfonic acid, under nitrogen system, stir at 55~80rpm rotating speed, heat up rapidly to 60~100 ℃ and react for 0.3 hours, then gradually heat up to 220 ℃ and heat preservation for 1 hour, and then react. The temperature was raised to 230-270°C and the reaction was carried out for about 2.2 hours, and the reaction was terminated when the amount of by-products produced reached 6.3 kg. Cool down to about 190°C, add 24g of antimony acetate and 15g of triphenyl phosphate, continue to heat up and slowly depressurize, adjust the rotational speed to 30~50rpm, control the temperature to between 255~285°C, and gradually reduce the pressure to below 100Pa. polycondensation reaction. Sampling and analysis...
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[0032] Example 2
[0033]19.9kg of terephthalic acid, 2.6kg of isophthalic acid, 7.1kg of dimethyl isophthalate-5-sodium sulfonate, 15.3kg of ethylene glycol and 4.4kg of caprolactone were put into the 100L stainless steel reactor, And add manganese acetate 32g, trifluoromethanesulfonic acid 35g, under nitrogen system, stir with 55~80rpm rotating speed, heat up rapidly to 70~110 ℃ after reaction 0.4 hour, be gradually warmed up to 230 ℃ insulation to carry out reaction 0.8 hour, then The temperature was raised to 245-275° C. to react for about 1.5 hours, and the reaction was terminated when the amount of by-products produced reached 6.1 kg. Cool down to about 190°C, add 25g of antimony acetate and 15g of triphenyl phosphate, continue to heat up and slowly depressurize, adjust the rotational speed to 35~45rpm, control the temperature to between 275~295°C, and gradually reduce the pressure to below 100Pa. polycondensation reaction. Sampling and analysis, when the viscosity of ...
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[0035] Example 3
[0036] 15.9kg of terephthalic acid, 7.9kg of isophthalic acid, 4.7kg of dimethyl isophthalate-5-sodium sulfonate, 16kg of ethylene glycol and 7.1kg of caprolactone were put into the 100L stainless steel reactor, and Add 23g of manganese acetate and 45g of methanesulfonic acid, stir with 60~70rpm rotating speed under nitrogen system, rapidly heat up to 65~120℃ and react for 0.45 hours, then gradually heat up to 225℃ and heat preservation for 1 hour, then heat up to 240 ℃ The reaction was carried out at ~270°C for about 1.8 hours, and the reaction was terminated when the amount of by-products produced reached 6.0 kg. Cool down to about 190°C, add 24g of germanium dioxide and 15g of triphenyl phosphate, continue to heat up and slowly depressurize, adjust the rotational speed to 40-50rpm, control the temperature to between 260-285°C, and gradually reduce the pressure to below 100Pa A polycondensation reaction is carried out. Sampling and analysis, when the vis...
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