Speciation of mobile arsenic in soil samples as a function of pH

被引:85
作者
PantsarKallio, M
Manninen, PKG
机构
[1] Lahti Research Laboratory, FIN-15210 Lahti
关键词
arsenic; mobile fraction; pH changes; wood-preservative plants;
D O I
10.1016/S0048-9697(97)00176-9
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Arsenic (as As2O5)-contaminated soil samples collected from wood-preservative plants were extracted at pH 1-13 and analyzed by ion chromatography-inductively coupled plasma mass spectrometry. The extraction conditions were chosen to simulate the pH changes occurring in the environmental waters or pH changes due to acidic or basic accidental leaks, in order to provide information about the mobile arsenic species in the environment. Only the mobile fraction of toxic metals in the soil can cause contamination and health risks. The highest amount of arsenic was extracted at the highest pH, i.e. pH 13. At pH 3-9, in the case of most samples, less than 2% of the total arsenic was extracted, which indicates that pH changes in the environment would have to be very dramatic if they were to release high amounts of arsenic bound to the soil. Only inorganic species, As(III) and As(V), were found in extractions and much higher concentrations of As(V) than As(III) were extracted in all cases. However, some species conversion had taken place, since also As(III) was found in extractions and in the original solution in wood-preservative plant arsenic was present as As2O5. Also the effects of different types of solutions and the ionic strength of the carbonate buffer in arsenic extraction were studied. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:193 / 200
页数:8
相关论文
共 24 条
[1]   DETERMINATION OF ARSENIC SPECIES IN FISH BY DIRECTLY COUPLED HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY-INDUCTIVELY COUPLED PLASMA-MASS SPECTROMETRY [J].
BRANCH, S ;
EBDON, L ;
ONEILL, P .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1994, 9 (01) :33-37
[2]  
CAROLI S, 1996, ELEMENTAL SPECIATION, P23
[3]   EXTRACTION TECHNIQUES FOR SELECTIVE DISSOLUTION OF AMORPHOUS IRON-OXIDES FROM SOILS AND SEDIMENTS [J].
CHAO, TT ;
ZHOU, L .
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL, 1983, 47 (02) :225-232
[4]   SPECIATION OF ARSENIC IN A CONTAMINATED SOIL BY SOLVENT-EXTRACTION [J].
CHAPPELL, J ;
CHISWELL, B ;
OLSZOWY, H .
TALANTA, 1995, 42 (03) :323-329
[5]   ARSENIC SPECIATION BY COUPLING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY [J].
DEMESMAY, C ;
OLLE, M ;
PORTHAULT, M .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1994, 348 (03) :205-210
[6]  
FURST A, 1983, NEW LOOK ARSENIC CAR
[7]   The importance of mobile, mobilisable and pseudo total heavy metal fractions in soil for three-level risk assessment and risk management [J].
Gupta, SK ;
Vollmer, MK ;
Krebs, R .
SCIENCE OF THE TOTAL ENVIRONMENT, 1996, 178 (1-3) :11-20
[8]   SEPARATION OF 7 ARSENIC COMPOUNDS BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH ONLINE DETECTION BY HYDROGEN ARGON FLAME ATOMIC-ABSORPTION SPECTROMETRY AND INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY [J].
HANSEN, SH ;
LARSEN, EH ;
PRITZL, G ;
CORNETT, C .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1992, 7 (04) :629-634
[9]   SPECIATION OF ARSENIC IN URINE USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRIC DETECTION [J].
HEITKEMPER, D ;
CREED, J ;
CARUSO, J .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1989, 4 (03) :279-284
[10]  
HODGSON E, 1988, DIRECTIONARY TOXICOL, P40