Viscoelasticity of near-critical silica-polyacrylamide hydrogel nanocomposites

被引:34
作者
Adibnia, Vahid [1 ]
Hill, Reghan J. [1 ]
机构
[1] McGill Univ, Dept Chem Engn, Montreal, PQ H3A005, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Hydrogel nanocomposite; Viscoelastiticy; Sol-gel transition; Polyacrylamide; CROSS-LINKING; NANOPARTICLE; PARTICLES; POLYMER; SUSPENSIONS; GELATION;
D O I
10.1016/j.polymer.2017.01.013
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The sol-gel transition of silica-polyacrylamide hydrogel nanocomposites is studied when approaching the gel point by independently varying the nanoparticle (NP) and chemical crosslinker concentrations. Time-concentration-superposition (TCS) principles are applied to ascertain the effect of NPs on dynamics at the gel point. Doping dilute and concentrated polyacrylamide (PA) solutions with silica NPs indicates that these particles do not crosslink PA; neither do they form percolating networks. Nevertheless, silica NPs interact with PA to influence the storage and loss moduli to a much greater degree than expected for passive fillers. Interestingly, when silica NPs are embedded in very weakly chemically crosslinked PA (with a bis crosslinker concentration that would otherwise not form PA hydrogels), they significantly enhance the effective degree of crosslinking, forming viscoelastic solids. From TCS analysis of dynamics at the gel point, the bond probability is found to scale with the NP volume fraction as p similar to phi(1.5), whereas chemical crosslinking furnishes a bond probability that is linear in the crosslinker concentration. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:457 / 465
页数:9
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