首页> 外文期刊>Journal of Polymers and the Environment >Chemically Modified Chitosan Bio-Sorbents for the Competitive Complexation of Heavy Metals Ions: A Potential Model for the Treatment of Wastewaters and Industrial Spills
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Chemically Modified Chitosan Bio-Sorbents for the Competitive Complexation of Heavy Metals Ions: A Potential Model for the Treatment of Wastewaters and Industrial Spills

机译:化学改性的壳聚糖生物吸附剂,用于重金属离子的竞争络合:一种治疗废水和工业泄漏的潜在模型

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Heavy metal pollution of water sources has become one of the most serious environmental and health problems nowadays. Chitosan (CHI) and derivatives can be used in the complexation and adsorption of heavy metals in water. Hence, this study compared the influence of CHI and carboxymethyl chitosan (CMC) ligands on the competitive complexation between toxic heavy metal ions with opposite charges Cr(VI) and Cd(II) at different pH values as an alternative and ecologically sustainable proposal for industrial spills of heavy metals into aquatic environments. The properties of the synthesized products and CHI were extensively characterized by several spectroscopy techniques, the competitive kinetics of complexation of metal ions with CHI and two type of CMC (with methanol, CMC 40_ME, and with ethanol, CMC 60_ET) was evaluated by wavelength dispersive X-ray fluorescence spectroscopy (WDXRF). The results clearly indicated the influence of the pH and ligands on the competitive complexation of the cationic or anionic ions. The results demonstrated that O-carboxymethylation of chitosan has occurred with a degree of functionalization of (1.20 +/- 0.02) and (0.88 +/- 0.02) for CMC 40_ME and CMC 60_ET, respectively, leading to the formation of CMC soluble in alkaline medium (pH range of 3.5pH6.5 and 4.0pH8.0 for CMC 40_ME and CMC 60_ET, respectively). In alkaline media, complexation of CMC 40_ME is approximately 10% higher (147.2 +/- 0.9mgg(-1)) than CMC 60_ET (99.8 +/- 2.9mgg(-1)) with Cd2+ ions at pH 8.5, and approximately 21% lower [(95 +/- 2mgg(-1)) and (96.3 +/- 2.8mgg(-1)) for CMC 40_ME and CMC 60_ET, respectively] than CHI (121 +/- 6mgg(-1)) for CrxO yz- ions at pH 3.0. The kinetic analysis showed variations for each ion and a significant difference regarding the complexant towards the negatively charged ions. The CMC 40_ME, in any analyzed pH, the complexation occurred during the first 45min of the process. These results showed that CMC, as polydentate functional ligand, was more efficient than CHI especially for the complexation of cations in basic media. Therefore, these systems appear to be attractive alternatives for the containment of industrial spills of heavy metals in wastewater.
机译:现在的水源的重金属污染已成为现在最严重的环境和健康问题之一。壳聚糖(Chi)和衍生物可用于水中重金属的络合和吸附。因此,该研究将Chi和羧甲基壳聚糖(CMC)配体对不同pH值(VI)和CD(II)的有毒重金属离子与不同pH值的竞争络合的影响,作为工业的替代和生态可持续的提案将重金属溢出到水生环境中。通过多波长分散评估合成产品和CHI的合成产品和CHI的性质,通过多种光谱技术,用CHI和两种CMC(用甲醇,CMC 40_ME和乙醇,CMC 60_ET)来络合金属离子络合的竞争动力学X射线荧光光谱(WDXRF)。结果清楚地表明了pH和配体对阳离子或阴离子离子的竞争络合的影响。结果表明,CMC 40_ME和CMC 60_ET的(1.20 +/- 0.02)和(0.88 +/- 0.02)的官能化程度,壳聚糖的O-羧甲基化分别发生,导致CMC溶于碱性的CMC中等(CMC 40_ME和CMC 60_ET的3.5ph6.5和4.0ph8.0的pH范围为3.5phph6.5和4.0ph0.0.et)。在碱性介质中,CMC 40_ME的络合比CMC 60_ET(99.8 +/- 2.9mgg(-1))高约10%(147.2 +/- 0.9mgg(-1)),pH 8.5的CD2 +离子,约21百分比[(95 +/- 2mgg(-1))和(96.3 +/- 2.8mgg(-1)),CMC 40_ME和CMC 60_ET,分别为CHI(121 +/- 6mgg(-1)) pH 3.0的Crxo Yzions。动力学分析显示了每个离子的变化以及对带负电离子的络合剂的显着差异。在任何分析的pH中,CMC 40_ME,在该过程的前45分钟期间发生络合。这些结果表明,CMC作为络胶质官能配体,比CHI更有效,特别是对于碱基培养基中的阳离子络合。因此,这些系统似乎是遏制废水中重金属产业泄漏的有吸引力的替代品。

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