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硫醇接枝壳聚糖凝胶珠对汞的吸附

Uptake of mercury by thiol-grafted chitosan gel beads.

作者信息

Merrifield John D, Davids William G, MacRae Jean D, Amirbahman Aria

机构信息

Department of Civil and Environmental Engineering, University of Maine, 5711 Boardman Hall, Orono, ME 04469-5711, USA.

出版信息

Water Res. 2004 Jul;38(13):3132-8. doi: 10.1016/j.watres.2004.04.008.

Abstract

This study describes the synthesis and characterization of thiol-grafted chitosan beads for use as mercury (Hg) adsorbents. Chitosan flakes were dissolved and formed into spherical beads using a phase inversion technique, then crosslinked to improve their porosity and chemical stability. Cysteine was grafted onto the beads in order to improve the adsorption affinity of Hg to the beads. The beads possessed an average diameter of 3.2 mm, porosity of 0.9, specific surface area of approximately 100 m2/g, average pore size of approximately 120 angstroms, and specific gravity of 2.0. Equilibrium and kinetic uptake experiments were conducted to study the uptake of Hg by the beads. The adsorption capacity was approximately 8.0 mmol-Hg/g-dry beads at pH 7, and decreased with decreasing pH. Hg adsorption kinetics was modeled as radial pore diffusion into a spherical bead with nonlinear adsorption. Use of the nonlinear Freundlich isotherm in the diffusion equation allowed modeling of the uptake kinetics with a single tortuosity factor of 1.5 +/- 0.3 as the fitting parameter for all initial Hg concentrations, chitosan loadings, and agitation rates. At agitation rates of 50 and 75 rpm, where uptake rate was reduced significantly due to the boundary layer effect, the mass transfer coefficient at the outside boundary was also used as a fitting parameter to model the kinetic data. At agitation rates higher than 150 rpm, pore diffusion was the rate-limiting step. The beads exhibited a high initial uptake rate followed by a slower uptake rate suggesting pore diffusion as the rate-determining step especially at high agitation rates. Higher uptake rates observed in this study compared to those in a previous study of chitosan-based crab shells indicate that dissolution and gel formation increase the porosity and pore accessibility of chitosan.

摘要

本研究描述了用作汞(Hg)吸附剂的硫醇接枝壳聚糖珠的合成与表征。壳聚糖薄片溶解后,采用相转化技术制成球形珠,然后进行交联以提高其孔隙率和化学稳定性。将半胱氨酸接枝到珠子上,以提高汞对珠子的吸附亲和力。珠子的平均直径为3.2毫米,孔隙率为0.9,比表面积约为100平方米/克,平均孔径约为120埃,比重为2.0。进行了平衡和动力学吸收实验,以研究珠子对汞的吸收情况。在pH值为7时,吸附容量约为8.0毫摩尔汞/克干珠,并随pH值降低而降低。汞吸附动力学被模拟为径向孔扩散进入具有非线性吸附的球形珠。在扩散方程中使用非线性弗伦德利希等温线,允许以1.5±0.3的单一曲折因子作为所有初始汞浓度、壳聚糖负载量和搅拌速率的拟合参数来模拟吸收动力学。在搅拌速率为50和75转/分钟时,由于边界层效应吸收速率显著降低,外部边界处的传质系数也用作拟合参数来模拟动力学数据。在搅拌速率高于150转/分钟时,孔扩散是限速步骤。珠子表现出较高的初始吸收速率,随后吸收速率较慢,表明孔扩散是限速步骤,尤其是在高搅拌速率下。与先前基于壳聚糖的蟹壳研究相比,本研究中观察到的较高吸收速率表明,溶解和凝胶形成增加了壳聚糖的孔隙率和孔可及性。

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