质子化
傅里叶变换红外光谱
X射线光电子能谱
壳聚糖
聚电解质
化学
胺气处理
酰胺
红外光谱学
离子键合
羧酸盐
分析化学(期刊)
高分子化学
物理化学
化学工程
有机化学
聚合物
离子
工程类
作者
Gwendolyn Lawrie,Imelda Keen,Barry R. Drew,A. F. Chandler-Temple,Llewellyn Rintoul,Peter M. Fredericks,Lisbeth Grøndahl
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2007-06-26
卷期号:8 (8): 2533-2541
被引量:1260
摘要
This study investigates alginate−chitosan polyelectrolyte complexes (PECs) in the form of a film, a precipitate, as well as a layer-by-layer (LbL) assembly. The focus of this study is to fully characterize, using the complementary techniques of Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS) in combination with solution stability evaluation, the interactions between alginate and chitosan in the PECs. In the FTIR spectra, no significant change in the band position of the two carbonyl vibrations from alginate occurs upon interaction with different ionic species. However, protonation of the carboxylate group causes a new band to appear at 1710 cm-1, as anticipated. Partial protonation of the amine group of chitosan causes the appearance of one new band (∼1530 cm-1) due to one of the −NH3+ vibrational modes (the other mode overlaps the amide I band). Importantly, the position of the two main bands in the spectral region of interest in partly protonated chitosan films is not dependent on the extent of protonation. XPS N 1s narrow scans can, however, be used to assess the degree of amine protonation. In our alginate−chitosan film, precipitate, and LbL assembly, the bands observed in the FTIR correspond to the species −COO- and −NH3+, but their position is not different from each of the single components. Thus, the conclusion of the study is that FTIR cannot be used directly to identify the presence of PECs. However, in combination with XPS (survey and narrow N 1s scans) and solution stability evaluation, a more complete description of the structure can be obtained. This conclusion challenges the assignment of FTIR spectra in the literature.
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