Reduction of silver solubility by humic acid and thiol ligands during acanthite (@b-Ag"2S) dissolution [An article from: Environmental Pollution]
Book Details
PublisherElsevier
ISBN / ASINB000RR3V7A
ISBN-13978B000RR3V72
AvailabilityAvailable for download now
MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from Environmental Pollution, published by Elsevier in 2005. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
Precipitation of highly insoluble metal sulfide minerals like acanthite (@b-Ag"2S) or red cinnabar (HgS) is in principle an effective means to reduce metal availability and toxicity in contaminated soils. Unfortunately, experiments have shown that red cinnabar may be solubilized in the presence of dissolved organic matter or thiol ligands. To determine whether the same applies to acanthite, a laboratory synthesized @b-Ag"2S mineral was incubated for up to 3 weeks in the presence of KNO"3, dissolved humic acids, cysteine, methionine and thiosulfate. XPS analysis identified Ag"2O (52%), Ag"2SO"4 (8%) and Ag"2S (40%) on the particle surfaces. Ag was released into solution in the presence of KNO"3 and methionine, presumably from mixed-oxidation surface layers. Contrary to earlier results with cinnabar, however, humic acids reduced Ag concentrations in solution by about 75%, and cysteine and thiosulfate, each containing a free -SH functional group, almost completely suppressed Ag release into solution.
Description:
Precipitation of highly insoluble metal sulfide minerals like acanthite (@b-Ag"2S) or red cinnabar (HgS) is in principle an effective means to reduce metal availability and toxicity in contaminated soils. Unfortunately, experiments have shown that red cinnabar may be solubilized in the presence of dissolved organic matter or thiol ligands. To determine whether the same applies to acanthite, a laboratory synthesized @b-Ag"2S mineral was incubated for up to 3 weeks in the presence of KNO"3, dissolved humic acids, cysteine, methionine and thiosulfate. XPS analysis identified Ag"2O (52%), Ag"2SO"4 (8%) and Ag"2S (40%) on the particle surfaces. Ag was released into solution in the presence of KNO"3 and methionine, presumably from mixed-oxidation surface layers. Contrary to earlier results with cinnabar, however, humic acids reduced Ag concentrations in solution by about 75%, and cysteine and thiosulfate, each containing a free -SH functional group, almost completely suppressed Ag release into solution.
