Method for the preparation of pentafluorophenylacrylate polymer
AssigneeChung-Shan Institute of Science and Technology
InventorsShean-Jeng Jong, Chang-Chih Lin, Yu-Sheng Lin
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Abstract
A method for synthesizing a pentafluorophenyl acrylate polymer includes bulk polymerizing a pentafluorophenyl acrylate monomer in the presence of a free radical initiator. The reactant mixture was subjected to an ultrasonication treatment, so that the mixing of the initiator and the monomer is enhanced; carried out the bulk polymerization at 25-99° C. for a period of time, and at 100-200° C. under a vacuum pressure for another period of time to complete the bulk polymerization, so that residue amounts of the initiator, unreacted monomer and oligomer of the monomer are reduced in the resulting reaction mixture.
Claims9
A process for preparing a pentafluorophenyl acrylate polymer by bulk polymerizing a reaction mixture comprising a pentafluorophenyl acrylate monomer and a radical initiator, wherein the radical initiator is not soluble in the pentafluorophenyl acrylate monomer, wherein the improvement comprises subjecting the reaction mixture to an ultrasonication treatment, so that the mixing of the initiator and the monomer is enhanced;
- carrying out the bulk polymerization at a first temperature of 25-200° C. for a first period of time;
- and carrying out the bulk polymerization at a second temperature of 25-200° C. under a vacuum pressure for a second period of time, wherein the second temperature is higher than the first temperature for another period of time, so that residue amounts of the radical initiator, unreacted monomer and oligomer of the monomer are reduced in the resulting product mixture.
A process for preparing a pentafluorophenyl acrylate homopolymer by bulk homopolymerizing a reaction mixture comprising a pentafluorophenyl acrylate monomer and a radical initiator, wherein the radical initiator is not soluble in the pentafluorophenyl acrylate monomer, wherein the improvement comprises subjecting the reaction mixture to an ultrasonication treatment, so that the mixing of the initiator and the monomer is enhanced;
- carrying out the bulk homopolymerization at a first temperature of 25-200° C. for a first period of time;
- and carrying out the bulk homopolymerization at a second temperature of 25-200° C. under a vacuum pressure for a second period of time, wherein the second temperature is higher than the first temperature for another period of time, so that residue amounts of the radical initiator, unreacted monomer and oligomer of the monomer are reduced in the resulting product mixture.
Dependencies are inferred from the claim text.