用FTIR光谱研究了静磁场下水溶液中聚氧乙烯的半胶化

E. Calabrò, S. Magazù
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引用次数: 32

摘要

采用傅里叶红外光谱研究了聚氧乙烯水溶液在200 mT静磁场作用4 h后,在25 mg/mL浓度下中红外区振动带的变化。对PEO溶液在3500 ~ 1000 cm−1范围内的FTIR光谱分析证实了醚带的伸缩振动、亚甲基的C-H对称-反对称振动和弯曲振动以及C-O-C伸缩带。暴露2h和4h后,对称和非对称拉伸CH2振动带强度显著降低,1465 cm−1附近平面CH2振动剪切弯曲强度显著降低。最后,1080 cm−1附近的C-O-C拉伸带在暴露4 h后强度增加。这一结果可归因于SMF暴露后PEO水溶液中分子间氢键的形成增加,这是由于PEO链在SMF暴露后发生了重定向。在这种情况下,观察到的CH2振动带强度的降低也是可以理解的,因为在施加SMF的情况下,PEO链的重定向引起了PEO的脱胶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Demicellization of Polyethylene Oxide in Water Solution under Static Magnetic Field Exposure Studied by FTIR Spectroscopy
FTIR spectroscopy was used to investigate the alterations of the vibration bands in the mid-infrared region of Polyethylene oxide in aqueous solution at 25 mg/mL concentration under exposure up to 4 h to a static magnetic field at 200 mT. FTIR spectroscopic analysis of PEO solution in the range 3500–1000 cm−1 evidenced the stretching vibrations of ether band, C–H symmetric-antisymmetric and bending vibrations of methylene groups, and the C–O–C stretching band. A significant decrease in intensity of symmetric and asymmetric stretching CH2 vibration bands occurred after 2 h and 4 h of exposure, followed by a significant decrease in intensity of scissoring bending in plane CH2 vibration around 1465 cm−1. Finally, the C–O–C stretching band around 1080 cm−1 increased in intensity after 4 h of exposure. This result can be attributed to the increase of formation of the intermolecular hydrogen bonding that occurred in PEO aqueous solution after SMF exposure, due to the reorientation of PEO chain after exposure to SMF. In this scenario, the observed decrease in intensity of CH2 vibration bands can be understood as well considering that the reorientation of PEO chain under the applied SMF induces PEO demicellization.
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