A modified ethylene-vinyl acetate copolymer pour point depressant
A vinyl acetate and copolymer technology, applied in the field of modified ethylene-vinyl acetate copolymer pour point depressant, can solve problems such as complex components, poor compatibility of high molecular polymers, and affecting the use effect of industrial devices, and achieve The effect of improving compatibility
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Embodiment 1
[0024] Step 1. Preparation of water phase
[0025] Add 1000Kg water and 2Kg polyoxyethylene alkyl ether sodium sulfate into a 2000L autoclave, and stir evenly.
[0026] Step 2. Preparation of oil phase
[0027] In a 200L reactor, mix 100Kg ethylene-vinyl acetate copolymer and 1Kg propenyl-1,3-sultone, then add 0.4Kg cumene hydroperoxide and 0.1Kg sodium bisulfate and stir well.
[0028] Step 3. Suspension Polymerization
[0029] Add the oil phase solution to the reaction kettle equipped with the prepared water phase in step 1, feed 0.5Kg of 2-cyclopentenyl-1-acetic acid, and then react at 50°C for 12 hours, discharge the material after the reaction, and dry to obtain product.
[0030] Step 4. Blending
[0031] The surface-modified ethylene-vinyl acetate copolymer obtained in step 3 of 85Kg is then mixed with 15Kg polycaprolactone to obtain the patented product. The number is T-1.
Embodiment 2
[0033] Step 1. Preparation of water phase
[0034] Add 1000Kg water and 0.5Kg polyoxyethylene alkyl ether sodium sulfate into a 2000L autoclave, and stir evenly.
[0035] Step 2. Preparation of oil phase
[0036] In a 200L reactor, mix 100Kg ethylene-vinyl acetate copolymer and 0.5Kg propenyl-1,3-sultone, then add 0.2Kg cumene hydroperoxide and 0.05Kg sodium bisulfate, and stir well .
[0037] Step 3. Suspension Polymerization
[0038] Add the oil phase solution to the reaction kettle equipped with the prepared water phase in step 1, pass in 0.1Kg of 2-cyclopentenyl-1-acetic acid, and then react at 40°C for 18 hours, discharge the material after the reaction, and dry to obtain product.
[0039] Step 4. Blending
[0040] 75Kg of the surface-modified ethylene-vinyl acetate copolymer obtained in step 3 is then mixed with 25Kg of polycaprolactone to obtain the patented product. The number is T-2.
Embodiment 3
[0042] Step 1. Preparation of water phase
[0043] Add 1000Kg water and 2Kg polyoxyethylene alkyl ether sodium sulfate into a 2000L autoclave, and stir evenly.
[0044] Step 2. Preparation of oil phase
[0045] In a 200L reactor, mix 100Kg ethylene-vinyl acetate copolymer and 2Kg propenyl-1,3-sultone, then add 0.6Kg cumene hydroperoxide and 0.2Kg sodium bisulfate, and stir evenly.
[0046] Step 3. Suspension Polymerization
[0047] Add the oil phase solution to the reaction kettle equipped with the prepared water phase in step 1, feed 1Kg of 2-cyclopentenyl-1-acetic acid, and then react at 70°C for 10 hours, discharge the material after the reaction, and dry to obtain the product .
[0048] Step 4. Blending
[0049] 90Kg of the surface-modified ethylene-vinyl acetate copolymer obtained in step 3 is then mixed with 10Kg of polycaprolactone to obtain the patented product. The number is T-3.
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