Method for preparing aromatic vinyl-unsaturated nitrile-based copolymer and aromatic vinyl-unsaturated nitrile-based copolymer prepared thereby
An aromatic vinyl, unsaturated technology, applied in the preparation of aromatic vinyl-unsaturated nitrile copolymers and the field of aromatic vinyl-unsaturated nitrile copolymers, can solve the lack of impact resistance and Heat resistance, low oligomer content and other issues, to achieve the effect of reducing residue generation, improving surface quality, and excellent heat resistance
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[0023] Specifically, the preparation method of the aromatic vinyl-unsaturated nitrile copolymer according to one embodiment of the present invention includes: adding aromatic vinyl monomers with a weight ratio of 65:35 to 78:22 to the reaction solvent monomers and unsaturated nitrile monomers to prepare a mixed solution, by adding to the mixed solution a polymerization initiator comprising an organic peroxide having a half-life temperature of 100° C. to 120° C. so that based on 100 parts by weight of all monomers , the content of the polymerization initiator is in the range of 0.01 parts by weight to 0.08 parts by weight, and then the polymerization is carried out at 115°C to 135°C so that the monomer conversion rate is more than 80%, to prepare the step of the polymerization product (step 1); and The polymer product is subjected to a devolatilization process to prepare an oligomer content of less than 0.5 parts by weight (based on 100 parts by weight of the copolymer), a resid...
Embodiment 1
[0062]A mixed solution was prepared by dissolving 71 parts by weight of styrene and 29 parts by weight of acrylonitrile in toluene (TLN). Here, toluene was used in an amount of 25 parts by weight based on 100 parts by weight of the total weight of all monomers. Furthermore, 0.05 parts by weight of 1,1-bis(tert-butylperoxy)cyclohexane as a polymerization initiator and 0.21 parts by weight of tert-dodecylmercaptan (TDDM) as a molecular weight regulator, and copolymerized at a reaction temperature of 130°C. The obtained polymer product was subjected to a devolatilization process at a temperature of 230° C. and a pressure of 20 Torr to prepare a styrene-acrylonitrile (SAN) copolymer.
[0063] Mix 73 parts by weight of the SAN copolymer thus prepared with 27 parts by weight of ABS DP (polybutadiene grafted with SAN), 0.25 parts by weight of antioxidant and 0.7 parts by weight of lubricant, and prepare heat-resistant permanent resin composition. The heat-resistant resin compositi...
Embodiment 2 to 5
[0065] Each SAN copolymer and heat-resistant resin composition were prepared in the same manner as in Example 1 except that the materials were used in the amounts listed in Table 1 below.
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