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单羧酸对壳聚糖膜结构及传输和力学性能的异常影响。

Unusual effects of monocarboxylic acids on the structure and on the transport and mechanical properties of chitosan films.

机构信息

KTH Royal Institute of Technology, School of Chemical Science and Engineering, Fibre and Polymer Technology, SE-100 44 Stockholm, Sweden.

Innventia, Box 5604, SE-11486 Stockholm, Sweden.

出版信息

Carbohydr Polym. 2015 Nov 5;132:419-29. doi: 10.1016/j.carbpol.2015.06.050. Epub 2015 Jun 25.

Abstract

The purpose of this study was to study the transport of monocarboxylic acids in chitosan films, since this is important for understanding and predicting the drying kinetics of chitosan from aqueous solutions. Despite the wealth of data on chitosan films prepared from aqueous monocarboxylic acid solutions, this transport has not been reported. Chitosan films were exposed to formic, acetic, propionic and butyric acid vapours, it was found that the rate of uptake decreased with increasing molecular size. The equilibration time was unexpectedly long, especially for propionic and butyric acid, nine months. A clear two-stage uptake curve was observed for propionic acid. Evidently, the rate of uptake was determined by acid-induced changes in the material. X-ray diffraction and infrared spectroscopy indicated that the structure of the chitosan acetate and buffered chitosan films changed during exposure to acid and during the subsequent drying. The dried films previously exposed to the acid showed less crystalline features than the original material and a novel repeating structure possibly involving acid molecules. The molar mass of the chitosan decreased on exposure to acid but tensile tests revealed that the films were always ductile. The films exposed to acid vapour (propionic and butyric acid) for the longest period of time were insoluble in the size-exclusion chromatography eluent, and they were also the most ductile/extensible of all samples studied.

摘要

本研究旨在研究单羧酸在壳聚糖膜中的传输,因为这对于理解和预测壳聚糖从水溶液中的干燥动力学非常重要。尽管有大量关于壳聚糖从单羧酸水溶液中制备的膜的数据,但这种传输尚未被报道。壳聚糖膜暴露于甲酸、乙酸、丙酸和丁酸蒸气中,发现吸收速率随分子尺寸的增加而降低。平衡时间出人意料地长,特别是对于丙酸和丁酸,需要九个月。对于丙酸,观察到明显的两阶段吸收曲线。显然,吸收速率由酸诱导的材料变化决定。X 射线衍射和红外光谱表明,壳聚糖醋酸盐和缓冲壳聚糖膜的结构在暴露于酸以及随后的干燥过程中发生了变化。先前暴露于酸的干燥膜显示出比原始材料更少的结晶特征,并且可能涉及酸分子的新型重复结构。壳聚糖的摩尔质量在暴露于酸时降低,但拉伸试验表明膜始终具有延展性。在最长时间内暴露于酸蒸气(丙酸和丁酸)的膜在尺寸排阻色谱洗脱液中不溶,并且它们也是所有研究样品中最柔韧/可拉伸的。

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