Description of the turbidity measurements near the phase transition temperature of poly(N-isopropyl acrylamide) copolymers:: the effect of pH, concentration, hydrophilic and hydrophobic content on the turbidity

被引:24
作者
Erbil, C [1 ]
Saraç, AS [1 ]
机构
[1] Istanbul Tech Univ, Dept Chem, TR-50626 Istanbul, Turkey
关键词
turbidity; coil-globule transition; poly(N-isopropyl acrylamide-itaconic acid) copolymers; poly(N-isopropyl acrylamide)s with siloxane end group;
D O I
10.1016/S0014-3057(02)00010-1
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Absorbance values between 300 and 800 nm of aqueous solutions of poly(N-isopropyl acrylamide-co-itaconic acid-9.80), poly(N-isopropyl acrylamide-co-itaconic acid-52.05) and poly(N-isopropyl acrylamide)s containing Tegomer H-Si 2111 end groups and/or blocks were measured using a Shimadzu 160-A UV-visible spectrometer. Turbidities obtained from these absorbance values were used to interpret the macromolecular phase transition from a hydrophilic to a hydrophobic structure of the polymers. The effects of comonomer type and content, concentration of the solutions, pH and temperature on the coil-globule transition were discussed in terms of turbidity form factor, beta related to size and shapes of particles and calculated by using the simplified form of Debye equation. The results presented in this work show that the presence of Tegomer H-Si 2111 (Si containing end groups and/or blocks) or high amount of itaconic acid (IA) in the chains prevent a collapse transition from hydrated extended coils to hydrophobic globules, which aggregate and form a separate phase (beta < 2). Furthermore, it was observed that in the case of concentrated solutions intermolecular hydrophobic interactions between isopropyl groups overcame the repulsive forces resulting from the ionized carboxylic acid groups of IA or surface active nature of Si containing hydrophobic groups (beta > 2). This stage of the transition corresponds to macroscopic phase separation after an intramolecular process. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1305 / 1310
页数:6
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