Influence of pH on the surface activity of humic acid: micelle-like aggregate formation and interfacial adsorption

被引:125
作者
Terashima, M
Fukushima, M
Tanaka, S [1 ]
机构
[1] Hokkaido Univ, Grad Sch Environm Earth Sci, Div Mat Sci, Sapporo, Hokkaido 0600810, Japan
[2] Natl Inst AIST, Tsukuba, Ibaraki 3058569, Japan
关键词
humic acid; surface activity; pH; micelle-like aggregation; interfacial adsorption;
D O I
10.1016/j.colsurfa.2004.08.028
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 influence of pH on the surface activity of humic acid (HA), was extracted from peat soil, was investigated by surface tension (gamma) measurement and the increase in solubility of p-dichlorobenzene (p-DCB). The gamma for an HA solution gradually decreased with increasing concentrations of HA. As the pH was decreased, the gamma versus HA concentration curve shifted into a lower HA concentration region. In these curves, the beginning of the plateau was in good agreement with the aggregation point of HA as evaluated by the enhanced solubility of p-DCB. The logarithmic concentration of HA at the aggregation point, gamma and the surface area occupied by an HA molecule decreased sigmoidally with decreasing pH. The aggregation point at pH 4 was 1/1.4 times that at pH 7. These results can be attributed to the acid dissociation behavior of the HA. The change in surface area occupied by an HA molecule may be due to both collaborative adsorption and a decrease in electrostatic repulsion between carboxyl groups at the air-water interface. The pC(20) value, which was used as one of hydrophobic parameters, sigmoidally increased with decreasing pH, and the pC(20) values at pH 4 and 5 were 1.3 times higher than those at pH 6 and 7. These results demonstrate that micelle-like aggregation and the interfacial adsorption of HA were substantially facilitated in the acidic region. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 83
页数:7
相关论文
共 37 条
[1]  
[Anonymous], 1996, METHODS SOIL ANAL 3, DOI DOI 10.2136/SSSABOOKSER5.3.C35
[2]   Volume and structure of humic acids studied by viscometry pH and electrolyte concentration effects [J].
Avena, MJ ;
Vermeer, AWP ;
Koopal, LK .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1999, 151 (1-2) :213-224
[3]   Kinetics of humic acid adsorption at solid-water interfaces [J].
Avena, MJ ;
Koopal, LK .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (16) :2739-2744
[4]   SURFACE-TENSION OF AQUEOUS-SOLUTIONS OF SOIL HUMIC SUBSTANCES [J].
CHEN, Y ;
SCHNITZER, M .
SOIL SCIENCE, 1978, 125 (01) :7-15
[5]   WATER SOLUBILITY ENHANCEMENT OF SOME ORGANIC POLLUTANTS AND PESTICIDES BY DISSOLVED HUMIC AND FULVIC-ACIDS [J].
CHIOU, CT ;
MALCOLM, RL ;
BRINTON, TI ;
KILE, DE .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1986, 20 (05) :502-508
[6]   Effects of humic substances on the bioavailability and aerobic biodegradation of polychlorinated biphenyls in a model soil [J].
Fava, F ;
Piccolo, A .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 77 (02) :204-211
[7]   Acid-base characterization of molecular weight fractionated humic acid [J].
Fukushima, M ;
Tanaka, S ;
Nakamura, H ;
Ito, S .
TALANTA, 1996, 43 (03) :383-390
[8]   Influence of humic substances on the removal of pentachlorophenol by a biomimetic catalytic system with a water-soluble iron (III) - Porphyrin complex [J].
Fukushima, M ;
Sawada, A ;
Kawasaki, M ;
Ichikawa, H ;
Morimoto, K ;
Tatsumi, K ;
Aoyama, M .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (05) :1031-1036
[9]   INTERPRETATION OF THE ACID-BASE-EQUILIBRIUM OF HUMIC-ACID BY A CONTINUOUS PK DISTRIBUTION AND ELECTROSTATIC MODEL [J].
FUKUSHIMA, M ;
TANAKA, S ;
HASEBE, K ;
TAGA, M ;
NAKAMURA, H .
ANALYTICA CHIMICA ACTA, 1995, 302 (2-3) :365-373
[10]   DOES HUMIC-ACID FORM A MICELLE [J].
GUETZLOFF, TF ;
RICE, JA .
SCIENCE OF THE TOTAL ENVIRONMENT, 1994, 152 (01) :31-35