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壳聚糖溶液温度诱导降解动力学数值模拟时MHS粘度常数的校正

Correction of MHS Viscosimetric Constants upon Numerical Simulation of Temperature Induced Degradation Kinetic of Chitosan Solutions.

作者信息

De Benedictis Vincenzo Maria, Soloperto Giulia, Demitri Christian

机构信息

DHITECH Scarl, Via Trinchese 61, Lecce 73100, Italy.

Department of Engineering for Innovation, University of Salento, Via Monteroni, km 1, Lecce 73100, Italy.

出版信息

Polymers (Basel). 2016 May 31;8(6):210. doi: 10.3390/polym8060210.

Abstract

The Mark⁻Houwink⁻Sakurada (MHS) equation allows for estimation of rheological properties, if the molecular weight is known along with good understanding of the polymer conformation. The intrinsic viscosity of a polymer solution is related to the polymer molecular weight according to the MHS equation, where the value of the constants is related to the specific solvent and its concentration. However, MHS constants do not account for other characteristics of the polymeric solutions, , Deacetilation Degree (DD) when the solute is chitosan. In this paper, the degradation of chitosan in different acidic environments by thermal treatment is addressed. In particular, two different solutions are investigated (used as solvent acetic or hydrochloric acid) with different concentrations used for the preparation of chitosan solutions. The samples were treated at different temperatures (4, 30, and 80 °C) and time points (3, 6 and 24 h). Rheological, Gel Permeation Chromatography (GPC), Fourier Transform Infrared Spectroscopy (FT-IR), Differential Scanning Calorimetry (DSC) and Thermal Gravimetric Analyses (TGA) were performed in order to assess the degradation rate of the polymer backbones. Measured values of molecular weight have been integrated in the simulation of the batch degradation of chitosan solutions for evaluating MHS coefficients to be compared with their corresponding experimental values. Evaluating the relationship between the different parameters used in the preparation of chitosan solutions (e.g., temperature, time, acid type and concentration), and their contribution to the degradation of chitosan backbone, it is important to have a mathematical frame that could account for phenomena involved in polymer degradation that go beyond the solvent-solute combination. Therefore, the goal of the present work is to propose an integration of MHS coefficients for chitosan solutions that contemplate a deacetylation degree for chitosan systems or a more general substitution degree for polymers in which viscosity depends not only on molecular weight and solvent combinations.

摘要

如果已知分子量并对聚合物构象有充分了解,Mark-Houwink-Sakurada(MHS)方程可用于估算流变性质。根据MHS方程,聚合物溶液的特性粘度与聚合物分子量相关,其中常数的值与特定溶剂及其浓度有关。然而,MHS常数并未考虑聚合物溶液的其他特性,例如当溶质为壳聚糖时的脱乙酰度(DD)。本文探讨了壳聚糖在不同酸性环境中通过热处理的降解情况。具体而言,研究了两种不同的溶液(用作溶剂的乙酸或盐酸),它们具有不同的浓度,用于制备壳聚糖溶液。样品在不同温度(4、30和80°C)和时间点(3、6和24小时)下进行处理。进行了流变学、凝胶渗透色谱(GPC)、傅里叶变换红外光谱(FT-IR)、差示扫描量热法(DSC)和热重分析(TGA),以评估聚合物主链的降解速率。测得的分子量值已整合到壳聚糖溶液间歇降解的模拟中,以评估MHS系数,并与相应的实验值进行比较。评估壳聚糖溶液制备中使用的不同参数(例如温度、时间、酸的类型和浓度)之间的关系,以及它们对壳聚糖主链降解的贡献,拥有一个能够解释聚合物降解过程中所涉及现象的数学框架非常重要,这些现象超出了溶剂-溶质组合的范畴。因此,本工作的目标是提出一种针对壳聚糖溶液的MHS系数整合方法,该方法考虑了壳聚糖体系的脱乙酰度,或者对于粘度不仅取决于分子量和溶剂组合的聚合物,考虑更一般的取代度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92da/6432309/44e55443289d/polymers-08-00210-g001.jpg

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