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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:通过kmno_4,hClO_4和HNO_3氧化还原对通过接枝共聚的淀粉纳米粒子的结构改性

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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:这里寻址的新颖性是为了使用我们以前制备的淀粉纳米粒子(SNP)约80-100nm作为用于使用KMnO 4,HCLO4在HNO3存在下以创新的氧化还原对的甲基丙烯酸(MAA)的起始基底。水性介质。这是为了看看SNP对分散良好的纳米粒子颗粒,大表面积,生物降解性和反应性的速度和程度的影响。除了;最大化移植物产量和移植反应效率,并降低均聚物形成以更低的程度。这可以通过深入评估进入影响聚合反应的主要因素,例如引发剂,单体,SNP和酸浓度,聚合时间和温度和液体比例。获得的结果表明,包括接枝产率,移植物反应效率和均聚物形成的聚合物产率的大小由这些因素确定。通过傅里叶变换红外光谱仪仪器确认所得共聚物的结构;虽然通过扫描电子显微镜,X射线衍射和热重分析表征表面形态,结晶结构和热性能。此外,通过镉离子评价所得共聚物作为环境修复材料,并在不同程度上从其溶液中除去阳离子染料;除了作为极性溶剂和盐酸作为酸性溶液的较高溶胀和耐化学性。报道了合成中涉及的预期机制。

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