Temperature dependent phase behavior of PNIPAM microgels in mixed water/methanol solvents

被引:94
作者
Kojima, Hiroyuki [1 ]
Tanaka, Fumihiko [1 ,2 ]
Scherzinger, Christine [3 ]
Richtering, Walter [3 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Polymer Chem, Kyoto 6158510, Japan
[2] Inst Theoret Polymer Sci, Kawasaki, Kanagawa 2150018, Japan
[3] Rhein Westfal TH Aachen, Inst Phys Chem, D-52056 Aachen, Germany
关键词
competitive hydrogen bonds; cononsolvency; dynamic light scattering; microgels; neutron scattering; poly(N-isopropylacylamide); solvent excess adsorption; solvent excess binding; N-ISOPROPYLACRYLAMIDE GELS; AQUEOUS-SOLUTIONS; POLY(N-ISOPROPYLACRYLAMIDE) GELS; CO-NONSOLVENCY; WATER; TRANSITION; METHANOL; CONONSOLVENCY; MIXTURES; DYNAMICS;
D O I
10.1002/polb.23194
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Temperature dependent phase behavior of poly(N-isopropylacylamide) (PNIPAM) microgels in water/methanol mixtures of different composition was studied with dynamic light scattering (DLS) and small-angle neutron scattering (SANS). Using DLS, it is possible to measure the diffusion coefficient, and thus the size of particles exactly and directly; the variation of the phase transition temperature in the different solvents is also easy to detect by this method. With SANS measurements in D2O/MeOD mixtures, some of the DLS results were confirmed. Moreover, SANS measurements give valuable information on the particle structure in different solvents. The experiments were compared with the theory of competitive hydration introduced by Tanaka et al. We found a good agreement of theory and experiment, and obtained the theoretical predictions: around the transition temperature, the composition of the bound methanol along the chains is higher than that of the outer solution, while the whole methanol composition inside the gel is lower. (c) 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym. Phys. 2013, 51, 1100-1111
引用
收藏
页码:1100 / 1111
页数:12
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