Wall-Rock Alteration in the Goldfield District, Nevada

Richard D. Harvey, Charles J. Vitaliano

The Journal of Geology · 1964 · 27 citations · 13 references

Concepts

Abstract

Hydrothermal alteration of early Tertiary dacite, andesite, and latite has produced the following miner-alogical zones which flank a complex system of gold-bearing veins: (1) propylitic zone farthest from the vein; (2) argillic zone, divided into a montmorillonite subzone in the outermost part, and an illite-kaolinite sub-zone in the innermost part; (3) alunite-quartz zone, immediately adjacent to the vein. The boundary between the alunite-quartz zone and the relatively thin illite-kaolinite subzone is sharp. The latter subzone grades into the relatively wide montmorillonite subzone. The degree of crystallinity of kaolinite increases and the polymorphic form of the 9.9 Å mica varies from lMd (illite) to 2M (K-mica) as the alunite-quartz zone is approached. The propylitic zone is characterized by chlorite (14 Å) and calcite. The gradational transition to the argillic zone is marked by the occurrence of a 1:1 mixed-layer chlorite-vermiculite. Alunite is believed to have formed by reaction of sulfuric acid and K-mica and the chemical reaction is believed to be \documentclass{aastex} \usepackage{amsbsy} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{bm} \usepackage{mathrsfs} \usepackage{pifont} \usepackage{stmaryrd} \usepackage{textcomp} \usepackage{portland,xspace} \usepackage{amsmath,amsxtra} \usepackage{wasysym} \pagestyle{empty} \DeclareMathSizes{10}{9}{7}{6} \begin{document}$$\mathrm{KAl_{3}Si_{10}(OH)_{2(s)} + 4H^{+}{}_{(aq)} + 2SO^{=}{}_{4(aq)} = KAl_{3}(SO_{4})_{2}(OH)_{6(s)} + 3SiO_{2(s)}},$$\end{document} where (s) and (aq) indicate the solid and aqueous state, respectively. The theoretical standard free energy of this reaction is approximately -42.1, -54, and -72 kcal/mole alunite at 25° C, 200° C, and 300° C, respectively. The uncertainty of the free energies is 3 kcal. at 25° C. and of the order of 10 kcal. at the higher temperatures. Consideration of the chemical kinetics of the decomposition of the illite is very important in the reaction.

References

13