Characterisation of novel modified active carbons and marine algal biomass for the selective adsorption of lead

被引:99
作者
Malik, DJ
Strelko, V
Streat, M [1 ]
Puziy, AM
机构
[1] Univ Loughborough, Dept Chem Engn, Loughborough LE11 3TU, Leics, England
[2] Inst Sorpt & Endoecol Problems, UA-03164 Kiev, Ukraine
关键词
oxidised carbons; phosphorus-containing carbon; algae; pK distribution function; selectivity; metal sorption;
D O I
10.1016/S0043-1354(01)00348-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This paper discusses the sorption performance of novel materials for the removal of lead(II) and copper(II) from near-neutral aqueous solutions. Active carbons with surface heteroatoms of oxygen and phosphorus have been prepared. The surface functional groups display weakly acidic ion exchange characteristics. The optimum solution pH for maximum metal sorption is related to the pK values of the surface functional groups. In oxygenated active carbons, pK values are not distinct but can be obtained by describing proton binding to the heterogeneous adsorbent surface as a continuous proton affinity distribution. Information derived from zeta-potential measurements combined with knowledge of the pK distribution function and concentration of surface functional groups has been used to explain the selectivity of oxidised active carbons towards lead(II) in the presence of copper(II) from multi-metal bearing solutions. Marine algal-based biosorbents have been challenged with lead(II) and copper(Il)-bearing wastewater. The weakly acidic carboxyl groups of structural polysaccharides present within the algal matrix display high sorption capacity for both metals. The negative surface charge of algal particles results in electrostatic interactions as well as coordination between metal species and the adsorbent surface. Proton affinity for the algal surface lowers the negative surface potential at pH values around 2. The surface functional groups in algae unlike those in oxidised active carbons may be represented by discrete acid-dissociation constant values. The influence of conformational differences in uronic-acid segments upon metal ion selectivity is discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1527 / 1538
页数:12
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