Preparation process of polypropylene resin special for thin-wall injection molding, prepared resin and application
A polypropylene resin and preparation process technology, applied in the field of polypropylene resin, can solve the problems of unsatisfactory impact resistance, aging resistance and transparency, too many transition materials, etc., to expand the scope of product application, good transparency, Use effects that have a long storage time
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Embodiment 1
[0058] The preparation method of vinyl chloride butenyl glycine copolymer M1 is as follows:
[0059] Spray the anti-sticking agent into the 5L reactor, and vacuumize the reactor three times until the pressure of the reactor is -0.7MPa. Add 2000g vinyl chloride monomer, 2000g R-4-butenyl glycine, 2040g deionized water, 12g alcoholysis degree 88% polyvinyl alcohol, 15g alcoholysis degree 72% polyvinyl alcohol, 1g alcoholysis degree 55% polyvinyl alcohol, 0.5g cumyl peroxyneodecanoate, 1g tert-butyl peroxydecanoate, the temperature of the reactor was raised to 56.8° C., and the polymerization reaction was started. Observe the pressure drop of the system during the reaction. After 2.5 hours of reaction, add 20ml of defoamer P875567 (polyether modified silicone oil, purchased from Shanghai McLean Biochemical Technology Co., Ltd.). When the system pressure drop reaches 0.15MPa(G), add 1g to stop the compounding (antioxidant 1076:antioxidant 245=1:1), the reactor pressure was releas...
Embodiment 2
[0061] The preparation method of vinyl chloride butenyl glycine copolymer M2 is as follows:
[0062] Spray anti-sticking agent into the 5L reactor, vacuumize the reactor three times until the pressure of the reactor is -0.7MPa, add 2000g vinyl chloride monomer, 1800g R-4-butenylglycine, 2040g Deionized water, 10g alcoholysis degree 88% polyvinyl alcohol, 10g alcoholysis degree 72% polyvinyl alcohol, 1g alcoholysis degree 55% polyvinyl alcohol, 0.5g cumyl peroxyneodecanoate, 2g decyl peroxide Acetate tert-butyl ester, the temperature of the reactor was raised to 56.8°C, and the polymerization reaction was started. Observe the pressure drop of the system during the reaction. After 2.5 hours of reaction, add 20ml of defoamer P875567 (polyether modified silicone oil, purchased from Shanghai Macklin Biochemical Technology Co., Ltd.). When the system pressure drop reaches 0.18MPa(G), add 1g to stop the compounding (antioxidant 1076:antioxidant 245=1:1), the pressure of the reactor ...
Embodiment 3
[0064] The preparation method of vinyl chloride butenyl glycine copolymer M3 is as follows:
[0065] Spray anti-sticking agent into the 5L reactor, vacuumize the reactor three times until the pressure of the reactor is -0.7MPa, add 2000g vinyl chloride monomer, 2500g R-4-butenylglycine, 2040g Deionized water, 15g alcoholysis degree 88% polyvinyl alcohol, 20g alcoholysis degree 72% polyvinyl alcohol, 1g alcoholysis degree 55% polyvinyl alcohol, 0.5g cumyl peroxyneodecanoate, 1g decyl peroxide Acetate tert-butyl ester, the temperature of the reactor was raised to 56.8°C, and the polymerization reaction was started. Observe the pressure drop of the system during the reaction. After 2.5 hours of reaction, add 20ml of defoamer P875567 (polyether modified silicone oil, purchased from Shanghai McLean Biochemical Technology Co., Ltd.). When the system pressure drop reaches 0.2MPa(G), add 1g to stop the compounding (antioxidant 1076:antioxidant 245=1:1), the pressure of the reactor wa...
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