REDOX REACTIONS ACCOMPANYING HYDROTHERMAL WALL ROCK ALTERATION

被引:26
作者
RAYMAHAS.BC
HOLLAND, HD
机构
[1] Department of Geological and Geophysical Sciences, Princeton University, Princeton, NJ
[2] Department of Civil Engineering, Indian Institute of Technology, Kanpur, U.P.
关键词
D O I
10.2113/gsecongeo.64.3.291
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
Wall rock alteration processes often include redox reactions involving iron and sulfur. The effect of these reactions on the composition of hydrothermal solutions can be represented conveniently on 1ogfs2-1ogfo2 diagrams. Contours of total dissolved sulfur concentration at 250° C and 350° C, calculated on the basis of the available thermochemical data and partially checked by direct experiment, were superimposed on the mineralogical boundaries of the Fe-S-O system in logf s2 - logfo 2 diagrams. During the replacement of iron oxides or silicates by pyrite, solutions containing a higher concentration of reduced than oxidized sulfur species move toward lower for values, whereas solutions containing a higher concentration of oxidized than reduced sulfur species move toward higher for values. The sequence of iron sulfide-iron oxide minerals in wall rock alteration zones depends both on the trend of these reaction paths and on the initial total dissolved sulfur concentration in the hydrothermal solutions. The observed sequences of minerals in alteration zones at Butte, in the northern part of the Boulder Batholith, and at Ely, Nevada, can be interpreted readily in terms of the proposed scheme. The concentration of total dissolved sulfur in the solutions in these three areas was probably less than 10 -2 moles/kg of solution. In the northern part of the Boulder Batholith the chemistry of the hydrothermal solutions was affected strongly both by cation metasomatism and by redox reactions. © 1969 Society of Economic Geologists, Inc.
引用
收藏
页码:291 / &
相关论文
共 32 条
[21]   BISULFATE ACID CONSTANT FROM 25 TO 225 DEGREES AS COMPUTED FROM SOLUBILITY DATA [J].
LIETZKE, MH ;
YOUNG, TF ;
STOUGHTON, RW .
JOURNAL OF PHYSICAL CHEMISTRY, 1961, 65 (12) :2247-&
[22]   2ND DISSOCIATION CONSTANT OF SULFURIC ACID FROM 25 TO 350 DEGREES EVALUATED FROM SOLUBILITIES OF CALCIUM SULFATE IN SULFURIC ACID SOLUTIONS [J].
MARSHALL, WL ;
JONES, EV .
JOURNAL OF PHYSICAL CHEMISTRY, 1966, 70 (12) :4028-&
[23]  
MEYER C, 1967, GEOCHEMISTRY HYDROTH, pCH6
[24]  
NORTON PJ, 1955, 55RL1248 GE RES LAB, P1
[25]  
PINCKNEY DM, 1965, THESIS PRINCETON U
[26]  
POLDERVAART A, 1955, 62 GEOL SOC AM SPEC, P119
[27]   SOLUBILITY OF HYDROGEN, OXYGEN, NITROGEN, AND HELIUM IN WATER - AT ELEVATED TEMPERATURES [J].
PRAY, HA ;
SCHWEICKERT, CE ;
MINNICH, BH .
INDUSTRIAL AND ENGINEERING CHEMISTRY, 1952, 44 (05) :1146-1151
[28]   COMPOSITION OF AQUEOUS SOLUTIONS IN EQUILIBRIUM WITH SULFIDES AND OXIDES OF IRON AT 350 DEGREES C [J].
RAYMAHASHAY, BC ;
HOLLAND, HD .
SCIENCE, 1968, 162 (3856) :895-+
[29]  
ROEDDER E, 1967, GEOCHEMISTRY HYDROTH, pCH12
[30]  
RYE RO, IN PRESS