TY - GEN
T1 - Dissolution of lead smelter dust compounds by humic acid
AU - Law, Kristen June
AU - Hiskey, J. B.
PY - 1990
Y1 - 1990
N2 - The ability of humic acids to complex metal ions is well established; however, the chemistry of lead dissolution and structure of the organo-metallic compound is not well understood. To better understand these problems, experiments were undertaken reacting the common smelter by-products PbSO4, PbCO3, and PbO with humic acid as a function of time, pH, and humic acid concentration. Examinations were made of the structure and mechanisms of complexing through the use of model humic acid functional group compounds and infra-red spectroscopy. Low pH conditions and increased humic acid concentrations favor PbO and PbCO3 complexing. Lead sulfate complexation was favored by increased pH and humic acid concentrations. At low pH values the particulate lead compounds adsorbed humic acid inhibiting lead dissolution. Active sites of complexation found through infra-red analysis were at carboxyl, phenol, phenyl, and aliphatic groups, along with formation of metalocyclohexanes and pentanes. Model functional group analysis proved inconclusive for characterization of active complexing sites.
AB - The ability of humic acids to complex metal ions is well established; however, the chemistry of lead dissolution and structure of the organo-metallic compound is not well understood. To better understand these problems, experiments were undertaken reacting the common smelter by-products PbSO4, PbCO3, and PbO with humic acid as a function of time, pH, and humic acid concentration. Examinations were made of the structure and mechanisms of complexing through the use of model humic acid functional group compounds and infra-red spectroscopy. Low pH conditions and increased humic acid concentrations favor PbO and PbCO3 complexing. Lead sulfate complexation was favored by increased pH and humic acid concentrations. At low pH values the particulate lead compounds adsorbed humic acid inhibiting lead dissolution. Active sites of complexation found through infra-red analysis were at carboxyl, phenol, phenyl, and aliphatic groups, along with formation of metalocyclohexanes and pentanes. Model functional group analysis proved inconclusive for characterization of active complexing sites.
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M3 - Conference contribution
AN - SCOPUS:0025684496
SN - 0873350901
T3 - Proc West Reg Symp Min Miner Process Wastes
SP - 61
EP - 67
BT - Proc West Reg Symp Min Miner Process Wastes
A2 - Doyle, Fiona M.
PB - Publ by Soc for Mining, Metallurgy & Exploration Inc
T2 - Proceedings of the Western Regional Symposium on Mining & Mineral Processing Wastes
Y2 - 30 May 1990 through 1 June 1990
ER -