Method for preparing vinyl chloride pasty resin
A technology of paste resin and vinyl chloride, which is applied in the field of microsuspension polymerization, can solve the problems of lower latex stability, lower drying efficiency, and increased burden of post-processing steps, and achieve the effect of improving yield and increasing output
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Embodiment 1
[0032] 110 kg of vinyl chloride, 110 kg of ionized water, 0.77 kg of sodium dodecylbenzenesulfonate and 1.1 kg of cetyl alcohol were added to a 300-liter pressure vessel and homogenized with a pressure homogenizer. The resulting aqueous dispersion was transferred to a 300-liter polymerization reactor containing 100 g of 2,2'-azobis(2,4-dimethylvaleronitrile), and the temperature was raised to 45°C to initiate polymerization.
[0033] Separately, 35 kg of a 1% by weight aqueous solution of sodium dodecylbenzenesulfonate was added to an 80-liter pressure vessel. After degassing, 40 kg of vinyl chloride was added to the container and dispersed with a homogenizer for 30 minutes to obtain a second dispersion for additional feeding.
[0034] After 3 hours, since the internal temperature of the reactor reached 45° C., continuous addition of the second dispersion at a rate of 6.0 kg / hour (3.2 kg monomer per hour) to the reactor was started. When 8 hours had elapsed, the continuous ad...
Embodiment 2
[0039] The procedure of Example 1 was repeated, except that when 2 hours passed, since the internal temperature of the reactor reached 45° C., the second dispersion was continuously added at a rate of 5.1 kg / hour (2.7 kg monomer per hour) . The total amount of the second dispersion added was 30.6 kg, of which the monomer portion was 16.3 kg. The polymerization conversion of the initially charged monomer was 15% at the time the addition of the second dispersion was started and 87% at the time the addition was terminated. With regard to the latex obtained finally, the conversion rate of all monomers was 93%. The results are listed in Table 1.
Embodiment 3
[0041] The procedure of Example 1 was repeated, except that when 1 hour passed, since the internal temperature of the reactor reached 45° C., the second dispersion was started to be continuously added at a rate of 5.1 kg / hour (2.7 kg monomer per hour) . The total amount of the second dispersion added was 35.7 kg, of which the monomer portion was 19.0 kg. The polymerization conversion of the initially charged monomer was 8% at the time the addition of the second dispersion was started and 89% at the time the addition was terminated. With regard to the latex obtained finally, the conversion rate of all monomers was 94%. The results are listed in Table 1.
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