Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You or Your Team.

Learn More →

Pyrite Formation in Organic‐rich Clay, Calcitic and Coal‐Forming Environments

Pyrite Formation in Organic‐rich Clay, Calcitic and Coal‐Forming Environments Abstract The early diagenetic characteristics of pyrite formation processes in a Miocene freshwater sequence of mixed sediments (coal fragments in clays, sandstones or shales) alternating with continuous brown coal layers was investigated. Based on abundant minerals, the following main sedimentary environments were distinguished: the illite‐montmorillonitic (I‐M), calcitic (Ct) and coal‐forming environment (CL). For these hydrogeochemically differing environments the effects of limiting factors on the pyrite formation process (availability of sulphate and Fe, amount of organic matter and participation of organic sulphur) were assessed by correlation analysis. Significant differences in the effects of these limiting factors in the particular environments were observed. These differences were explained taking in account the different oxidative activity, Fe‐complex and surface complex forming properties of humic substances in dependence of pH of environment and the abundance of sorptionally active clay minerals. In environments having a relatively low pH and containing clay minerals (I‐M‐and CL‐environments) the oxidative activity of humic substances (Hs) on pyrite precursors was greatly prevented however pyrite formation depended on reactive Fe availability as the consequence of complex formation. On the contrary, in environments with a relatively high pH, as it was the calcitic, the oxidative activity of Hs was greatly enhanced, thus oxidizing the sulfur precursors of pyrite. The oxidation degree of organic matter was probably also a consequence of the differing activity of the humic electron‐acceptors. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Acta Geologica Sinica (English Edition) Wiley

Pyrite Formation in Organic‐rich Clay, Calcitic and Coal‐Forming Environments

Loading next page...
 
/lp/wiley/pyrite-formation-in-organic-rich-clay-calcitic-and-coal-forming-YhuKdAj9yf

References (75)

Publisher
Wiley
Copyright
2006 Geological Society of China
ISSN
1000-9515
eISSN
1755-6724
DOI
10.1111/j.1755-6724.2006.tb00278.x
Publisher site
See Article on Publisher Site

Abstract

Abstract The early diagenetic characteristics of pyrite formation processes in a Miocene freshwater sequence of mixed sediments (coal fragments in clays, sandstones or shales) alternating with continuous brown coal layers was investigated. Based on abundant minerals, the following main sedimentary environments were distinguished: the illite‐montmorillonitic (I‐M), calcitic (Ct) and coal‐forming environment (CL). For these hydrogeochemically differing environments the effects of limiting factors on the pyrite formation process (availability of sulphate and Fe, amount of organic matter and participation of organic sulphur) were assessed by correlation analysis. Significant differences in the effects of these limiting factors in the particular environments were observed. These differences were explained taking in account the different oxidative activity, Fe‐complex and surface complex forming properties of humic substances in dependence of pH of environment and the abundance of sorptionally active clay minerals. In environments having a relatively low pH and containing clay minerals (I‐M‐and CL‐environments) the oxidative activity of humic substances (Hs) on pyrite precursors was greatly prevented however pyrite formation depended on reactive Fe availability as the consequence of complex formation. On the contrary, in environments with a relatively high pH, as it was the calcitic, the oxidative activity of Hs was greatly enhanced, thus oxidizing the sulfur precursors of pyrite. The oxidation degree of organic matter was probably also a consequence of the differing activity of the humic electron‐acceptors.

Journal

Acta Geologica Sinica (English Edition)Wiley

Published: Aug 1, 2006

There are no references for this article.