Nanoscavenger based dispersion preconcentration; sub-micron particulate extractants for analyte collection and enrichment

被引:40
作者
Howard, AG [1 ]
Khdary, NH
机构
[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[2] Minist Hlth, Mecca, Saudi Arabia
关键词
D O I
10.1039/b506242j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new approach has been developed for the preconcentration of analytes from solution using nanoscavengers; monodisperse functionalised particles of sub-micron dimensions, that can be suspended as a quasi-stable sol in an aqueous solution, and quantitatively recovered with the analyte by conventional filtration. No external agitation of the sample is required as the particles move naturally through the sample by Brownian motion, convection and sedimentation. By careful choice and control of their particle size and surface chemistries, nanoscavengers can be designed to suit a number of different analytical problems. Surface modification of these nanometre-sized particles, through the grafting of complexing or partitioning functional groups, can produce nanoscavengers having affinities for specific analytes and operating through a wide range of mechanisms from covalent bonding to hydrophobic interaction. The approach is illustrated by the development of an extraction-based preconcentration of metals from solution that employs sub-micron Stober-type silica spheres, the surfaces of which have been modified using chelating diamine and dithiocarbamate groups. The concept has potentially widespread applicability as it is neither limited to metal extractions, nor to the use of silica-based nanoscavengers. Minimal involvement of organic solvents make nanoscavengers a potentially environmentally benign ("green'') alternative to many conventional solvent extraction techniques.
引用
收藏
页码:1432 / 1438
页数:7
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共 41 条
[1]   Separation and preconcentration in a batch mode of Cd(II), Cr(III, VI), Cu(II), Mn(II, VII) and Pb(II) by solid-phase extraction by using of silica modified with N-propylsalicylaldimine [J].
Abou-El-Sherbini, KS ;
Kenawy, IMM ;
Hamed, MA ;
Issa, RM ;
Elmorsi, R .
TALANTA, 2002, 58 (02) :289-300
[2]  
AKATSUKA K, 1993, BUNSEKI KAGAKU, V42, P423
[3]   TiO2 nanosized powders by TiCl4 laser pyrolysis [J].
Alexandrescu, R ;
Dumitrache, F ;
Morjan, I ;
Sandu, I ;
Savoiu, M ;
Voicu, I ;
Fleaca, C ;
Piticesu, R .
NANOTECHNOLOGY, 2004, 15 (05) :537-545
[4]   Synthesis of sub-200 nm silsesquioxane particles using a modified Stober sol-gel route [J].
Arkhireeva, A ;
Hay, JN .
JOURNAL OF MATERIALS CHEMISTRY, 2003, 13 (12) :3122-3127
[5]   PREPARATION OF MONODISPERSE SILICA PARTICLES - CONTROL OF SIZE AND MASS FRACTION [J].
BOGUSH, GH ;
TRACY, MA ;
ZUKOSKI, CF .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 1988, 104 (01) :95-106
[6]   AGGREGATIVE GROWTH OF SILICA FROM AN ALKOXYSILANE IN A CONCENTRATED-SOLUTION OF AMMONIA [J].
BURNEAU, A ;
HUMBERT, B .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1993, 75 :111-121
[7]   Kinetics of formation of monodisperse colloidal silica particles through the hydrolysis and condensation of tetraethylorthosilicate [J].
Chen, SL ;
Dong, P ;
Yang, GH ;
Yang, JJ .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1996, 35 (12) :4487-4493
[8]  
Das RP, 2004, INDIAN J PHYS PT-A, V78A, P165
[9]   Surfacial, liquid sorption and monolayer-forming properties of hydrophilic and hydrophobic Stober silica particles [J].
Dékány, I ;
Németh, J ;
Szekeres, M ;
Schoonheydt, R .
COLLOID AND POLYMER SCIENCE, 2003, 282 (01) :1-6
[10]   A chemically bonded adsorbent for separation of antimony, copper and lead [J].
Deorkar, NV ;
Tavlarides, LL .
HYDROMETALLURGY, 1997, 46 (1-2) :121-135