Oxidative degradation of triblock-copolymer surfactant and its effects on self-assembly

被引:6
作者
Fussell, S. L. [1 ,3 ,4 ]
King, S. M. [2 ]
Royall, C. P. [1 ,3 ,4 ,5 ]
van Duijneveldt, J. S. [1 ]
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[2] STFC Rutherford Appleton Lab, ISIS Pulsed Neutron & Muon Source, Harwell Campus, Didcot OX11 0QX, Oxon, England
[3] Univ Bristol, HH Wills Phys Lab, Tyndall Ave, Bristol BS8 1TL, Avon, England
[4] Univ Bristol, Bristol Ctr Funct Nanomat, Tyndall Ave, Bristol BS8 1TL, Avon, England
[5] Univ PSL, ESPCI Paris, Gulliver UMR CNRS 7083, F-75005 Paris, France
基金
欧盟地平线“2020”; 欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
Surfactant; Self-assembly; Gelation; THERMAL-DEGRADATION; AQUEOUS-SOLUTIONS; POLY(ETHYLENE OXIDE); TEMPERATURE; STABILITY; GELATION;
D O I
10.1016/j.jcis.2021.08.045
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We investigate the degradation behaviour of a triblock-copolymer surfactant made from polyethylene oxide (PEO) and polypropylene oxide (PPO) (PEO-PPO-PEO), highlighting how the aggregation behaviour of this polymer in water alters with ageing. Samples aged at room temperature were compared to sam-ples degraded using accelerated ageing at elevated temperatures. We find that large mass losses occurred to the polymer surfactant which resulted in a change in the aggregation behaviour, with larger, rod-like or planar aggregates forming at longer degradation times. We look at how this change in aggregation behaviour changes the formulation stability of these polymers, specifically, the interaction of the polymer surfactant with poly(N-isopropylacrylamide) microgels. It is known that these species associate and form gels at elevated temperatures. This paper highlights how commonly used polymeric surfactants can degrade over time, resulting in dramatic changes to aggregation behaviour and therefore, formulation properties. (c) 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:953 / 960
页数:8
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