Reacción #1006001

ord-814c85078e9745ccb9216d94c7389a87

Ecuación de reacción

C=CC(=O)OCCCCCC(C)C
isooctyl acrylate
CC(C)(C#N)N=NC(C)(C)C#N
Vazo
C=COC(C)=O
vinyl acetate
CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C
2,2′-azobis(2,4-dimethylpentanenitrile)
C=CC(N)=O
acrylamide
C=CC(=O)OCCCCCC(C)C.C=CC(N)=O.C=COC(C)=O
Isooctyl Acrylate Acrylamide Vinyl Acetate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA master batch was prepared
  2. 2
    OtroThe bottle was purged for two minutes with nitrogen at a flow rate of one liter per minute
  3. 3
    OtroThe bottle was sealed
  4. 4
    workup.WAITplaced in a rotating water bath at 45° C. for twenty-four hours
  5. 5
    Otropolymerization

Procedimiento

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 Ng in ethyl acetate at a concentration of 0.15 g/dl. Its Brookfield viscosity was 5580 centipoise.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09271973B2uspto-grants-2016_03