Natural realgar and amorphous AsS oxidation kinetics

被引:64
作者
Lengke, MF
Tempel, RN [1 ]
机构
[1] Univ Nevada, Mackay Sch Mines, Dept Geol Sci, Reno, NV 89557 USA
[2] Univ Nevada, Grad Program Hydrol Sci, Reno, NV 89557 USA
关键词
D O I
10.1016/S0016-7037(02)01227-9
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
The oxidation rates of natural realgar and amorphous synthetic AsS by dissolved oxygen were evaluated using mixed flow reactors at pH 7.2 to 8.8 and dissolved oxygen contents of 5.9 to 16.5 ppm over a temperature range of 25 to 40degreesC. The ratios of As/S are stoichiometric for all amorphous AsS oxidation experiments except for two experiments conducted at pH similar to8.8. In these experiments, stoichiometric ratios of As/S were only observed in the early stages of AsS (am) oxidation whereas lower As/S ratios were observed during steady state. For realgar oxidation experiments, the As/S ratio is less than the stoichiometric ratio of realgar, ranging between 0.61 and 0.71. This nonstoichiometric release of As and S to solution indicates that realgar oxidation is more selective for S after the rates of oxidation become constant. All measured oxidation rates at 25degreesC can be described within experimental uncertainties as follows: [GRAPHICS] where R signifies the steady-state oxidation rate (mol m(-2) s(-1)), [DO] is dissolved oxygen concentration (M), and [H+] is the proton concentration (M). Arsenic (111) and As(V) are both present in solution, and As(III) is the dominant species in most experiments. Intermediate sulfur species besides sulfate, sulfite, and thiosulfate are the important products during realgar and AsS (am) oxidation. Comparison of realgar and AsS (am) oxidation rates shows that at similar conditions, the rates of AsS (am) are always faster by about a factor ranging from 2 to 38. The oxidation of realgar involves breaking bonds in the realgar crystal, whereas AsS (am) oxidation does not include crystallographic framework destruction due to the amorphous nature of the solid. Copyright (C) 2003 Elsevier Science Ltd.
引用
收藏
页码:859 / 871
页数:13
相关论文
共 24 条
[1]  
Barrante J.R., 1998, APPL MATH PHYS CHEM, P179
[2]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[3]   THE SURFACE OXIDATION OF PYRITE [J].
BUCKLEY, AN ;
WOODS, R .
APPLIED SURFACE SCIENCE, 1987, 27 (04) :437-452
[4]  
Craig J.R., 1981, ORE MICROSCOPY ORE P, V2nd
[5]  
DOUGLASS DL, 1992, AM MINERAL, V77, P1266
[6]  
Ehrlich H.L., 1963, ECON GEOL, V58, P991
[7]  
FORNERIS R, 1969, AM MINERAL, V54, P1062
[8]  
HUGI M, 1988, THESIS U BERN SWITZE
[9]  
Lasaga AC, 1981, REV MINERAL, P135, DOI DOI 10.1515/9781501508233-008
[10]   Electrochemical study of orpiment (As2S3) and realgar (As2S2) in acidic medium [J].
Lazaro, I ;
Gonzalez, I ;
Cruz, R ;
Monroy, MG .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (12) :4128-4132