Effects of pH and phosphate on the adsorptive fractionation of purified Aldrich humic acid on kaolinite and hematite

被引:52
作者
Hur, J
Schlautman, MA [1 ]
机构
[1] Clemson Univ, Sch Environm, Dept Environm Engn & Sci, Clemson, SC 29634 USA
[2] Clemson Univ, Sch Environm, Dept Geol Sci, Clemson, SC 29634 USA
[3] Clemson Univ, Clemson Inst Environm Toxicol, Pendleton, SC 29670 USA
基金
美国国家科学基金会;
关键词
humic substances; molecular weight fractionation; size exclusion chromatography; mineral surface; adsorption;
D O I
10.1016/j.jcis.2004.04.046
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The molecular weight (M-w) fractionation of purified Aldrich humic acid (PAHA) resulting from adsorption on kaolinite and hematite was investigated for different solution pH and phosphate conditions. Adsorption was highly pH-dependent, with higher uptake at lower pH values. For all pH conditions, the weight-average MW (MWw) of residual PAHA remaining in solution after adsorption deviated from the original M-w, indicating that preferential adsorption of certain M-w components occurred. The extent of preferential adsorption depended on the percent carbon adsorption at a given pH condition. For similar percent carbon adsorption ranges, a greater extent of preferential adsorption of the higher M-w PAHA components was observed with higher pH values as demonstrated by the lowest residual MWw value occurring at pH 9. Detailed analyses of selected residual PAHA samples clearly showed that adsorption selectivity for particular M-w components was strongly influenced by solution pH. The extent of preferential adsorption of lower M-w PARA components decreased in the presence of a small amount of phosphate. This effect was more evident for hematite than kaolinite, and became greater with lower solution pH irrespective of the mineral type. The different fractionation patterns observed for PAHA were reasonably well explained by the physicochemical trends occurring in its MWw fractions and the underlying sorption processes. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:264 / 270
页数:7
相关论文
共 31 条
[1]  
[Anonymous], 1994, HUMUS CHEM GENESIS C
[2]  
[Anonymous], 1984, SURFACE CHEM SOIL
[3]   Reaction of forest floor organic matter at goethite, birnessite and smectite surfaces [J].
Chorover, J ;
Amistadi, MK .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2001, 65 (01) :95-109
[4]   ADSORPTION OF NATURAL DISSOLVED ORGANIC-MATTER AT THE OXIDE WATER INTERFACE [J].
DAVIS, JA .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1982, 46 (11) :2381-2393
[5]  
DAVIS JA, 1981, ENVIRON SCI TECHNOL, V26, P1388
[6]   MACROMOLECULAR STRUCTURES OF HUMIC SUBSTANCES [J].
GHOSH, K ;
SCHNITZER, M .
SOIL SCIENCE, 1980, 129 (05) :266-276
[7]   ADSORPTION AND DESORPTION OF NATURAL ORGANIC-MATTER ON IRON-OXIDE - MECHANISMS AND MODELS [J].
GU, BH ;
SCHMITT, J ;
CHEN, ZH ;
LIANG, LY ;
MCCARTHY, JF .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1994, 28 (01) :38-46
[8]   Using selected operational descriptors to examine the heterogeneity within a bulk humic substance [J].
Hur, J ;
Schlautman, MA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (05) :880-887
[9]   Molecular weight fractionation of humic substances by adsorption onto minerals [J].
Hur, J ;
Schlautman, MA .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2003, 264 (02) :313-321
[10]  
ILIES E, 2004, COLLOID SURF A, V230, P99