梯度洗脱高效液相色谱法表征纤维素酯的化学异构性

IF 0.2 4区 化学 Q4 CHEMISTRY, ANALYTICAL
Tadatomo Kawai, Shizuka Ukita, S. Shimamoto
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引用次数: 0

摘要

开发了一种梯度聚合物洗脱色谱法(GPEC),该方法可以在宽取代度(DS)范围内分离乙酸纤维素(CA)。通过平均取代度为0.6至2.9的CA样品的丙酰化或苯甲酰化合成了一系列乙酸丙酸纤维素和乙酸苯甲酸纤维素样品,并使用GPEC方法进行了成分分离。基于吸附/解吸机理的反相梯度分离,使用乙腈∶H2O=6∶1和乙酸乙酯的线性梯度,苯基修饰的硅胶柱作为固定相。对于两个样品系列,实现了具有不同DS值的样品的分离。在低DS样品的洗脱过程中观察到轻微的摩尔质量效应。此外,在高DS样品的低保留时间下观察到尖锐的峰。尽管为了确定定量取代度分布,需要搜索进一步的分离系统,但该方法适用于在宽DS范围内确定DS分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of Chemical Heterogeneity of Cellulose Esters by Gradient Elution HPLC
A gradient polymer elution chromatography (GPEC) method was developed that can separate cellulose acetate (CA) with respect to a wide range of degrees of substitution (DS). A series of cellulose acetate propionate and cellulose acetate benzoate samples were synthesized by propionylation or benzoylation of CA samples with average degrees of substitution ranging from 0.6 to 2.9, and compositionally separated using the GPEC method. The reversed-phase gradient separation based on an adsorption/desorption mechanism, a linear gradient of acetonitrile : H 2 O = 6 : 1 and ethyl acetate was used with a phenyl group-modified silica column as stationary phase. Separation of samples with different DS values was achieved for both sample series. A slight molar mass effect was observed during elution for the sample with low DS. In addition, a sharp peak at low retention time was observed for the high DS sample. Although a search for further separation systems is necessary for the determination of quantitative substitution degree distribution, this method is applicable to the determination of DS distribution over a wide DS range.
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来源期刊
Bunseki Kagaku
Bunseki Kagaku 化学-分析化学
CiteScore
0.30
自引率
0.00%
发文量
64
审稿时长
3 months
期刊介绍: Bunsekikagaku is a journal written in Japanese and is published monthly by The Japan Society for Analytical Chemistry. The journal publishes papers on all aspects of the theory and practice of analytical sciences, including fundamental and applied, inorganic and organic, wet chemical and instrumental methods.
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