乳液聚合
木筏
高分子化学
化学
聚合
链式转移
乳状液
可逆加成-断裂链转移聚合
自组装
化学工程
自由基聚合
有机化学
聚合物
工程类
作者
Steven Thompson,Thiago R. Guimarães,Per B. Zetterlund
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2020-06-19
卷期号:21 (11): 4577-4590
被引量:24
标识
DOI:10.1021/acs.biomac.0c00685
摘要
Polymerization-induced self-assembly (PISA) and amphiphilic-macroRAFT-mediated emulsion polymerization are commonly used approaches for synthesis of well-defined polymers and sophisticated particle morphologies. One aspect of these systems that remains relatively unexplored is the conformational state of macroRAFT agents in aqueous solution. To redress this deficiency, we have used fluorescence spectrometry experiments to conduct detailed investigations of the coil conformation across a wide range of pH values for a series of poly(acrylic acid) (PAA) and poly(methacrylic acid) (PMAA) macroRAFT agents with different Z-groups (-S-(CH2)2-COOH, -S-(CH2)3-CH3, and -S-(CH2)11-CH3), as well as amphiphilic macroRAFT agents (PMAA-b-poly(methyl methacrylate)(PMMA) and PAA-b-polystyrene(PS)). The critical aggregate concentrations (CAC) or critical micelle concentrations (CMC) for all systems ranged from 7.48 × 10–7 to 2.57 × 10–3 mol L–1. Overall, an extensive library of CAC/CMC values has been compiled for PAA- and PMAA-based macroRAFT agents at different pH conditions, providing important information related to the mechanistic understanding and optimization of macroRAFT-assisted emulsion polymerization.
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