AQUEOUS STABLE FREE RADICAL POLYMERIZATION PROCESSES

Your Location：

Home >

Browse articles >

AQUEOUS STABLE FREE RADICAL POLYMERIZATION PROCESSES

Papers | Updated：2021-06-21

- AQUEOUS STABLE FREE RADICAL POLYMERIZATION PROCESSES
- AQUEOUS STABLE FREE RADICAL POLYMERIZATION PROCESSES
- 高分子科学（英文版） 2004年22卷第4期页码：309-312
- Affiliations：
- Author bio：
- Funds：
- DOI：
  中图分类号：
- 纸质出版：2004-08-20
- Accepted：
Scan QR Code
AQUEOUS STABLE FREE RADICAL POLYMERIZATION PROCESSES[J]. 高分子科学（英文版）, 2004,22(4):309-312.

AQUEOUS STABLE FREE RADICAL POLYMERIZATION PROCESSES[J]. 2004, 22(4): 309-312.
AQUEOUS STABLE FREE RADICAL POLYMERIZATION PROCESSES[J]. 高分子科学（英文版）, 2004,22(4):309-312. DOI：

AQUEOUS STABLE FREE RADICAL POLYMERIZATION PROCESSES[J]. 2004, 22(4): 309-312. DOI：

摘要

An overview of aqueous polymerizations

which include emulsion

miniemulsion and suspension polymerizations

under stable free radical polymerization (SFRP) conditions is presented. The success of miniemulsion and suspension SFRP polymerizations is contrasted with the difficulties associated with obtaining a stable emulsion polymerization. A recently developed unique microprecipitation technique is referenced as a means of making submicron sized particles that can be used to achieve a stable emulsion SFRP process.

Abstract

An overview of aqueous polymerizations

which include emulsion

miniemulsion and suspension polymerizations

关键词

Keywords

references

浏览量

Downloads

CSCD

文章被引用时，请邮件提醒。

Submit

工具集

关联资源

Multiple-Responsive Chiral Hydrogels from Helical Dendronized Poly(phenylacetylene)s

Squaramide-directed Cooperative One-dimensional Assembly in Telechelic Polydimethylsiloxane for Hierarchical Network Formation

Tunable Circularly Polarized Luminescence of Helical Poly(phenylacetylene)s via Side-chain-to-Backbone Förster Resonance Energy Transfer

A Paradigm for BF3 Co-initiated Cationic Polymerization with Low Dispersity: Introducing Acetonitrile and Lowering the Reaction Temperature

Alternating Poly(ether-alt-ester)s with High Glass Transition Temperature Enabled by Rotationally Constrained Biaryl Units