Benzoyl Peroxide → HCID 21225556, compound

HRID 1941051Notes

Reaction equation

HRID 1941051 reaction equation
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9]([O:13]CCCC)(=[O:12])[CH:10]=[CH2:11].C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C1(C)C(C)=CC=CC=1>[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9]([O-:13])(=[O:12])[CH:10]=[CH2:11]

Participants

5

Procedure

15 Parts of the above-obtained polymer resin having a higher molecular weight, 6 parts of a Fischer-Tropsch wax formed from natural gas (FT-100, melting point 91° C., supplied by Shell MDS (Malaysia) Sdn. Bhd.) and 100 parts of xylene were charged into a flask, and dissolved. The inner atmosphere of the flask was replaced with nitrogen gas, and the mixture was heated up to the boiling point of xylene. While the mixture was stirred under the reflux of xylene, a mixture containing 67 parts of styrene, 12 parts of n-butyl acrylate and 3 parts of benzoyl peroxide (polymerization initiator) were dropwise added over 2 hours to carry out a solution polymerization. After the addition was completed, the reaction mixture was aged for 1 hour with stirring under the reflux of xylene, to give a styrene/acrylate copolymer resin having molecular weight maximal values, measured by GPC, of 8,000 and 1.2×106 and containing 15% by weight of the polymer having a higher molecular weight, for use in an electrophotographic toner of the present invention.

Workup

  1. additionwere charged into a flask
  2. dissolutiondissolved
  3. additionwere dropwise added over 2 hours
  4. customa solution polymerization
  5. additionAfter the addition
  6. stirringwith stirring under the

Sources & evidence

ORD record
ord-39fd7074c1734ff791c8c1634c9cac29
Source dataset
uspto-grants-1997_12
Patent number
US05702859

Reaction notes

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