Short-range structure in (partially) crystalline potato starch determined with attenuated total reflectance Fourier-transform IR spectroscopy

衰减全反射 化学 淀粉 结晶度 无定形固体 吸光度 差示扫描量热法 结晶学 傅里叶变换红外光谱 红外线的 光谱学 分析化学(期刊) 红外光谱学 光学 色谱法 有机化学 量子力学 热力学 物理
作者
J.J.G. van Soest,H. Tournois,D. de Wit,Johannes F.G. Vliegenthart
出处
期刊:Carbohydrate Research [Elsevier]
卷期号:279: 201-214 被引量:1032
标识
DOI:10.1016/0008-6215(95)00270-7
摘要

A fast and direct method, based on infrared spectroscopy, for quantitative determination of starch short-range structure has been developed. The IR spectrum of starch is sensitive to changes in short-range structure in the C—C and C—O stretching region at 1300-800 cm−1. The IR absorbance band at 1047 cm−1 is sensitive to the amount of ordered or crystalline starch and the band at 1022 cm−1 is characteristic of amorphous starch. The ratios (R) of the heights of the bands at 1047 and 1022 cm−1, which expresses the amount of ordered starch to amorphous starch, and 1047 and 1035 cm−1, which is a measure of the amount of ordered starch, showed a linear regression with the amount of potato starch having B-type crystallinity as determined with wide-angle X-ray diffractometry. The IR spectrum and thus the short-range order is also sensitive to water content. In particular, the band at 994 cm−1, which is related to intramolecular hydrogen bonding of the hydroxyl group at C-6, is water sensitive. It is possible to quantify the IR data in terms of short-range order (SIR) over a range of 10–50% water. The method has been applied to quantify the changes in short-range structure during the melting of potato starch with 18 or 26% (w/w) water. The amount of short-range structure and the changes during melting in the (partially) destructured starch samples concur with differential scanning calorimetry and wide-angle X-ray diffractometry measurements.
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