참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Azobisisobutyronitrile | HCID 6547 | — |
| 반응물 | Acrylamide | HCID 6579 | — |
| 반응물 | Vinyl Acetate | HCID 7904 | — |
| 반응물 | 2,2'-Azobis(2,4-dimethylvaleronitrile) | HCID 91537 | — |
| 반응물 | Isooctyl acrylate | HCID 165746 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Ethylacetate methanol | HCID 21584119 | — |
| 생성물 | Isooctyl Acrylate Acrylamide Vinyl Acetate | HCID 86608178 | — |
반응 단계
A master batch was prepared by combining 621.0 g of isooctyl acrylate, 41.4 g of acrylamide, 165.6 g of vinyl acetate, 1.656 g of 2,2′-azobis(2,4-dimethylpentanenitrile) (available from the DuPont Company as Vazo™ 52), 884.52 g of ethyl acetate and 87.48 g of methanol. A 400 g portion of the resulting solution was placed in an amber quart bottle. The bottle was purged for two minutes with nitrogen at a flow rate of one liter per minute. The bottle was sealed and placed in a rotating water bath at 45° C. for twenty-four hours to effect essentially complete polymerization. The copolymer was diluted with 250 g of ethyl acetate/methanol (90/10) to 26.05% solids and had a measured inherent viscosity of 1.27 dl/g in ethyl acetate at a concentration of 0.15 g/dl. Its Brookfield viscosity was 5580 centipoise.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08242155B2 |
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| 출처 데이터셋 | uspto-grants-2012_08 |
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| ORD ID | ord-88c5ce84192a48a98cf94001c0143135 |
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| 출처 메모 | uspto-grants-2012_08 |
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