Thermo-responsive diblock and triblock cationic copolymers at the silica/aqueous interface: A QCM-D and AFM study

被引:7
|
作者
Moghaddam, Saeed Zajforoushan [1 ]
Zhu, Kaizheng [2 ]
Nystrom, Bo [2 ]
Thormann, Esben [1 ]
机构
[1] Tech Univ Denmark, Dept Chem, DK-2800 Lyngby, Denmark
[2] Univ Oslo, Dept Chem, POB 1033, N-0315 Oslo, Norway
基金
瑞典研究理事会;
关键词
Poly(N-isopropylacrylamide); Poly(ethylene glycol); Cationic copolymer; Dynamic light scattering; Quartz crystal microbalance with dissipation; Atomic force microscopy; QUARTZ-CRYSTAL MICROBALANCE; ATOMIC-FORCE MICROSCOPE; N-ISOPROPYL ACRYLAMIDE; DRUG-DELIVERY; AQUEOUS-SOLUTIONS; BLOCK-COPOLYMERS; BIOMEDICAL APPLICATIONS; PHASE-TRANSITION; SILICA NANOPARTICLES; POLY(ETHYLENE OXIDE);
D O I
10.1016/j.jcis.2017.06.044
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
The properties of synthesized diblock poly(N-isopropylacrylamide)-poly((3-acrylamidopropyl)trimethy lammonium chloride) and triblock methoxy-poly(ethylene glycol)-poly(N-isopropylacrylamide)-poly((3 -acrylamidopropyl)trimethylammonium chloride) cationic copolymers at the silica/aqueous interface are investigated using quartz crystal microbalance with dissipation monitoring (QCM-D) and atomic force microscopy (AFM). Moreover, dynamic light scattering is employed to assess the copolymers in terms of the hydrodynamic size and interchain aggregation. Although viscoelastic Voigt modeling of the QCM-D data suggests a comparable layer thickness for the copolymers on the silica surface, the AFM imaging and colloidal probe measurements reveal significant differences in surface coverage and thickness of the layers, which are discussed and compared with respect to the stabilization effect by the hydrophilic poly(ethylene glycol) block. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:546 / 555
页数:10
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