Hydration mechanism on a poly(methacrylic acid) film studied by in situ attenuated total reflection infrared spectroscopy

被引:19
|
作者
Tajiri, Tomokazu [1 ,2 ]
Morita, Shigeaki [3 ]
Ozaki, Yukihiro [1 ]
机构
[1] Kwansei Gakuin Univ, Dept Chem, Sch Sci & Technol, Sanda, Hyogo 6691337, Japan
[2] Astellas Pharma Inc, Pharmaceut Anal Pharmaceut Res & Technol Labs, Technol, Shizuoka 4250072, Japan
[3] Nagoya Univ, EcoTopia Sci Inst, Aichi 4648603, Japan
关键词
Poly(methacrylic acid) (PMAA); Hydrogen bonding; Hydration; HYDROGEN-BONDING INTERACTION; POLARIZED IR-SPECTRA; ACETIC-ACID; FORMIC-ACID; AB-INITIO; RAMAN; WATER; SORPTION; STATES; DIMER;
D O I
10.1016/j.polymer.2009.09.060
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A drastic structure change during a hydration process of a poly(methacrylic acid) (PMAA) film was observed by time-resolved in situ attenuated total reflection infrared (ATR-IR) spectroscopy. Inter- or intra-hydrogen-bonds via side-chain carboxyl groups are formed as cyclic dimers, side-on dimers and linear open chain oligomers including open dimers in a dried PMAA film. By contacting water, the side-chain hydrogen-bonds in PMAA are dissociated instantly, and then the subsequent carboxyl groups which have no hydrogen-bond newly hydrate with water molecules in a side-on form. Quantum chemical calculations (QCCs) using a model monomer of propionic acid (PA) also support the hydrogen-bonded and hydrated structures explored by the ATR-IR spectroscopy. It has been concluded from the present study that the dissociation of hydrogen-bonded and newly created hydrated structures via the carboxyl groups play an important role for the swelling of PMAA in water. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5765 / 5770
页数:6
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