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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Vinyl Acetate → Vinyl Acetate

HRID 1090
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HRID 1090 반응식
[C:1]([O:4][CH:5]=[CH2:6])(=[O:3])[CH3:2].[OH-].[NH4+]>CO>[CH:1]([OH:3])=[CH2:2].[C:1]([O:4][CH:5]=[CH2:6])(=[O:3])[CH3:2]
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참가 물질

5

반응물 2

HCID 7904Vinyl AcetateHCID 14923Ammonium Hydroxide

생성물 2

HCID 7904Vinyl AcetateHCID 11199Vinyl alcohol

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

This Example shows the preparation of high TFE content copolymer. The conditions of Example III were repeated except that a total of 470 mg of APS was added, the TFE addition rate was 0.01 lb/min (4.5 g/min), the vinyl acetate addition rate was 2 ml/min., and the final agitation rate was 80 rpm. 2580 g of a 25.0 wt % solids colloidal dispersion was obtained. To 100 g of the isolated, dried polymer was added 500 ml of methanol and 40 ml of concentrated ammonium hydroxide. After several weeks at room temperature with occasional shaking, the resulting solution was heated to remove the reaction by-products and there was obtained a hazy, viscous solution of 19 wt % solids of approximate composition 82 wt % TFE, 16 wt % vinyl alcohol, and 2 wt % vinyl acetate. Upon evaporation of the solvent at 50° C. in a vacuum oven for one day, a clear, somewhat rubbery melt fabricable polymer was obtained.

후처리

  1. customthe preparation of high TFE content copolymer
  2. additionwas added
  3. additionthe TFE addition rate
  4. custom2580 g of a 25.0 wt % solids colloidal dispersion was obtained
  5. waitAfter several weeks at room temperature with occasional shaking
  6. temperaturethe resulting solution was heated
  7. customto remove the reaction by-products

출처 및 근거

ORD 기록
ord-5fccfb36b4f847b99c3306f4dc04bee7
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05723556

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