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首页> 外文期刊>Journal of Polymers and the Environment >Structural Modification of Starch Nanoparticles Via Graft Copolymerization Using KMnO_4, HClO_4 and HNO_3 Redox Pair
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Structural Modification of Starch Nanoparticles Via Graft Copolymerization Using KMnO_4, HClO_4 and HNO_3 Redox Pair

机译:使用KMnO_4,HClO_4和HNO_3氧化还原对通过接枝共聚对淀粉纳米颗粒进行结构改性

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摘要

The novelty addressed here is commenced with a view to use our formerly prepared starch nanoparticles (SNPs) of size around 80-100nm as a starting substrate for grafting meth acrylic acid (MAA) using KMnO4, HClO4 in presence of HNO3 as innovative redox pair in aqueous medium. This was done to see the effect of SNPs with respect to well-dispersed nanosized particles, large surface areas, biodegradability and reactivity on the rate and extent of grafting. Besides; maximize the graft yield and graft reaction efficiency and reduce the homopolymer formation to lower extent. This could be accomplished via an in-depth assessment into the chief factors affecting the polymerization reaction such as initiator, monomer, SNPs and acid concentrations, time and temperature of polymerization, and liquor ratio. The results obtained indicate that the magnitude of the polymer yield including graft yield, graft reaction efficiency and homopolymer formation are determined by these factors. The structure of the resultant copolymers was confirmed instrumentally by Fourier transforms infrared spectroscopy; while both the surface morphology, crystalline structure and thermal properties were characterized by scanning electron microscopy, X-ray diffraction and thermal gravimetric analysis. Furthermore, the resultant copolymers were evaluated as environmental remediation materials via cadmium ions and cationic dyes removal from their solutions with different extent; in addition to higher swelling and chemical resistance in water as polar solvent and hydrochloric acid as acidic solution. The anticipated mechanisms involved in the synthesis are reported.
机译:为了解决这一问题,我们开始使用以前制备的大小为80-100nm左右的淀粉纳米颗粒(SNP)作为起始底物,使用KMnO4和HClO4在HNO3作为创新氧化还原对存在下接枝甲基丙烯酸(MAA)。水性介质。这样做是为了观察SNPs对均匀分散的纳米级颗粒,大表面积,生物降解性和反应性对接枝速率和程度的影响。除了;使接枝产率和接枝反应效率最大化,并减少均聚物的形成。这可以通过对影响聚合反应的主要因素进行深入评估来完成,例如引发剂,单体,SNP和酸浓度,聚合时间和温度以及液比。所得结果表明,由这些因素决定了包括接枝产率,接枝反应效率和均聚物形成在内的聚合物产率的大小。所得共聚物的结构通过傅里叶变换红外光谱仪进行了仪器确认。通过扫描电子显微镜,X射线衍射和热重分析对表面形貌,晶体结构和热性能进行了表征。此外,所得共聚物通过不同程度地从其溶液中脱除镉离子和阳离子染料被评价为环境修复材料。除了在水中作为极性溶剂和在盐酸作为酸性溶液时具有更高的溶胀性和耐化学性外。报告了参与合成的预期机理。

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