以戊二醛和三聚磷酸为交联剂合成壳聚糖磁性纳米颗粒

Indri Alidha Rahmani, Ani Mulyasuryani, U. Andayani
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引用次数: 0

摘要

壳聚糖是一种丰富的天然聚合物,具有吸附Pb2+的功能。然而,壳聚糖的缺点是在酸碱条件下不稳定,需要交联。本文将比较戊二醛(GD)和三聚磷酸盐(TPP)两种交联剂的使用,以解决这些问题。在酸性条件下加入戊二醛,在碱性条件下加入TPP共沉淀法合成壳聚糖磁性纳米颗粒。结果表明,FTIR光谱的特征波段为3131.96 cm-1 (OH和NH)、1635.86 cm-1 (C=O)、1401.97 cm-1 (CN)、~1110 cm-1 (COC)和~617 cm-1 (Fe-O)。SEM分析表明,CMNP-GA颗粒聚集的表面形貌比CMNP-TPP更明显。通过PSA分析确定了合成的纳米颗粒的尺寸,分别为131.95µm和137.10µm。XRD分析结果表明,制备的CMNP除含有Fe3O4相和壳聚糖相外,还含有γFe2O3相,认为这是Fe3O4氧化引起的
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of Chitosan Magnetic Nanoparticles using Glutaraldehyde and Tripolyphosphate as Crosslinker
Chitosan is an abundant natural polymer, which able to adsorb Pb2+. However, chitosan has the drawback of being unstable in acid and alkaline conditions, so it needs cross-linking. In this article, we will compare the usage of two crosslinkers, glutaraldehyde (GD) and tripolyphosphate (TPP), to solve these issues. The synthesis of chitosan magnetic nanoparticles was carried out by co-precipitation with the addition of glutaraldehyde under acidic conditions and the addition of TPP under alkaline conditions. The results showed that the FTIR spectrum gave characteristic bands at 3131.96 cm-1 (OH and NH), 1635.86 cm-1 (C=O), 1401.97 cm-1 (CN), ~1110 cm-1 (COC), and ~617 cm-1 (Fe-O). SEM analysis showed that the surface morphology of CMNP-GA particle aggregation was clear more than that of CMNP-TPP. The size of the synthesized nanoparticles was determined by PSA analysis, which was 131.95 µm and 137.10 µm, respectively. The results of the XRD analysis showed that, in addition to the Fe3O4 and chitosan phases, the produced CMNP also contained γFe2O3 phase, which was considered to be caused by Fe3O4 oxidation
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