Synthesis and properties of grafted copolymers of xanthan and glucomannan with acrylic monomers

Anton K. Smirnov, A. Shipovskaya
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Abstract

Graft copolymers of polysaccharides with acrylic monomers combine biodegradability, biocompatibility, the environmental friendliness of natural polymers and the increased thermal stability, chemical and mechanical resistance of synthetic polymers. This paper describes our search and analysis of the literature in English for 2002–2022 devoted to the graft polymerization of acrylamide, acrylic acid and 2-acrylamido- 2-methylpropanesulfonic acid onto xanthan and glucomannan macromolecular chains. It has been found that the synthesis of grafted copolymer chains proceeds by a radical polymerization mechanism using thermal homolytic decomposition of the initiator or microwave irradiation, or radiation initiation and frontal polymerization in some cases. Depending on the method of the reaction, the synthesis time of a graft copolymer varies from several minutes to several hours. The influence of the synthesis conditions and parameters on the monomer conversion, structure and properties of the resulting polymer has been considered. It has been found that decreasing the polysaccharide/monomer ratio and increasing the initiator concentration raise the efficiency and degree of grafting. Several methods for characterization of graft copolymers are discussed, including: IR spectroscopy to analyze the chemical structure of a sample, scanning electron microscopy to characterize structure, supramolecular ordering and porosity, differential thermal analysis to evaluate thermal effects and thermal stability. The effect of the synthesis conditions and the pH of the sorption medium on the water absorption and sorption capacity of this class of graft copolymers are discussed. The broad potential of graft copolymers for repeated cycles of absorption and release of liquid medium without loss of functional properties has been found. This opens prospects for the use of graft copolymers of xanthan and glucomannan with acrylic monomers as materials for water purification from metal ions and cationic dyes, targeted delivery and prolonged action of drugs and wound coatings for wound treatment.
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黄原胶与葡甘露聚糖接枝丙烯酸单体共聚物的合成及性能研究
多糖与丙烯酸单体的接枝共聚物结合了天然聚合物的生物可降解性、生物相容性和环境友好性,以及合成聚合物的热稳定性、耐化学性和耐机械性。本文描述了我们对2002-2022年关于丙烯酰胺、丙烯酸和2-丙烯酰胺- 2-甲基丙磺酸在黄原胶和葡甘露聚糖大分子链上接枝聚合的英文文献的搜索和分析。已有研究发现,接枝共聚物链的合成是通过引发剂的热均裂分解或微波辐照进行自由基聚合,或在某些情况下采用辐射引发和正面聚合的方式进行的。根据反应方法的不同,接枝共聚物的合成时间从几分钟到几个小时不等。考察了合成条件和参数对单体转化率、聚合物结构和性能的影响。研究发现,降低多糖/单体比和增加引发剂浓度可提高接枝效率和接枝程度。讨论了几种表征接枝共聚物的方法,包括:红外光谱分析样品的化学结构,扫描电子显微镜表征结构,超分子有序度和孔隙度,差热分析评价热效应和热稳定性。讨论了合成条件和吸附介质pH对该类接枝共聚物吸水性和吸附性能的影响。接枝共聚物具有广泛的潜力,可以在不损失功能特性的情况下对液体介质进行反复循环的吸收和释放。这为黄原胶和葡甘露聚糖与丙烯酸单体的接枝共聚物作为金属离子和阳离子染料的水净化材料、药物的靶向递送和延长作用以及伤口治疗的伤口涂层开辟了前景。
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