Evaluating the Potential of Scaling due to Calcium Compounds in Hydrometallurgical Processes
A fundamental theoretical and experimental study on calcium sulphate scale formation in hydrometallurgical solutions containing various minerals was conducted. A new database for the Mixed Solvent Electrolyte (MSE) model of the OLI Systems® software was developed through fitting of existing literatu...
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ndltd-TORONTO-oai-tspace.library.utoronto.ca-1807-246722013-11-01T04:10:43ZEvaluating the Potential of Scaling due to Calcium Compounds in Hydrometallurgical ProcessesAzimi, GhazalCalcium sulphateGypsumAnhydriteHemihydrateChemical ModellingSolubility measurementsTransformation mechanismTransformation kineticsHydrometallurgyScalingLaterite Pressure Acid LeachingSolid phase transformation0542A fundamental theoretical and experimental study on calcium sulphate scale formation in hydrometallurgical solutions containing various minerals was conducted. A new database for the Mixed Solvent Electrolyte (MSE) model of the OLI Systems® software was developed through fitting of existing literature data such as mean activity, heat capacity and solubility data in simple binary and ternary systems. Moreover, a number of experiments were conducted to investigate the chemistry of calcium sulphate hydrates in laterite pressure acid leach (PAL) solutions, containing Al2(SO4)3, MgSO4, NiSO4, H2SO4, and NaCl at 25–250ºC. The database developed, utilized by the MSE model, was shown to accurately predict the solubilities of all calcium sulphate hydrates (and hence, predict scaling potential) in various multicomponent hydrometallurgical solutions including neutralized zinc sulphate leach solutions, nickel sulphate–chloride solutions of the Voisey’s Bay plant, and laterite PAL solutions over a wide temperature range (25–250°C). The stability regions of CaSO4 hydrates (gypsum, hemihydrate and anhydrite) depend on solution conditions, i.e., temperature, pH and concentration of ions present. The transformation between CaSO4 hydrates is one of the common causes of scale formation. A systematic study was carried out to investigate the effect of various parameters including temperature, acidity, seeding, and presence of sulphate/chloride salts on the transformation kinetics. Based on the results obtained, a mechanism for the gypsum–anhydrite transformation below 100°C was proposed. A number of solutions for mitigating calcium sulphate scaling problems throughout the processing circuits were recommended: (1) operating autoclaves under slightly more acidic conditions (~0.3–0.5 M acid); (2) mixing recycled process solutions with seawater; and (3) mixing the recycling stream with carbonate compounds to reject calcium as calcium carbonate. Furthermore, aging process solutions, saturated with gypsum, with anhydrite seeds at moderate temperatures (~80°C) would decrease the calcium content, provided that the solution is slightly acidic.Papangelakis, Vladimiros G.2010-062010-08-04T14:46:59ZNO_RESTRICTION2010-08-04T14:46:59Z2010-08-04T14:46:59ZThesishttp://hdl.handle.net/1807/24672en_ca |
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language |
en_ca |
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NDLTD |
topic |
Calcium sulphate Gypsum Anhydrite Hemihydrate Chemical Modelling Solubility measurements Transformation mechanism Transformation kinetics Hydrometallurgy Scaling Laterite Pressure Acid Leaching Solid phase transformation 0542 |
spellingShingle |
Calcium sulphate Gypsum Anhydrite Hemihydrate Chemical Modelling Solubility measurements Transformation mechanism Transformation kinetics Hydrometallurgy Scaling Laterite Pressure Acid Leaching Solid phase transformation 0542 Azimi, Ghazal Evaluating the Potential of Scaling due to Calcium Compounds in Hydrometallurgical Processes |
description |
A fundamental theoretical and experimental study on calcium sulphate scale formation in hydrometallurgical solutions containing various minerals was conducted. A new database for the Mixed Solvent Electrolyte (MSE) model of the OLI Systems® software was developed through fitting of existing literature data such as mean activity, heat capacity and solubility data in simple binary and ternary systems. Moreover, a number of experiments were conducted to investigate the chemistry of calcium sulphate hydrates in laterite pressure acid leach (PAL) solutions, containing Al2(SO4)3, MgSO4, NiSO4, H2SO4, and NaCl at 25–250ºC. The database developed, utilized by the MSE model, was shown to accurately predict the solubilities of all calcium sulphate hydrates (and hence, predict scaling potential) in various multicomponent hydrometallurgical solutions including neutralized zinc sulphate leach solutions, nickel sulphate–chloride solutions of the Voisey’s Bay plant, and laterite PAL solutions over a wide temperature range (25–250°C).
The stability regions of CaSO4 hydrates (gypsum, hemihydrate and anhydrite) depend on solution conditions, i.e., temperature, pH and concentration of ions present. The transformation between CaSO4 hydrates is one of the common causes of scale formation. A systematic study was carried out to investigate the effect of various parameters including temperature, acidity, seeding, and presence of sulphate/chloride salts on the transformation kinetics. Based on the results obtained, a mechanism for the gypsum–anhydrite transformation below 100°C was proposed.
A number of solutions for mitigating calcium sulphate scaling problems throughout the processing circuits were recommended: (1) operating autoclaves under slightly more acidic conditions (~0.3–0.5 M acid); (2) mixing recycled process solutions with seawater; and (3) mixing the recycling stream with carbonate compounds to reject calcium as calcium carbonate. Furthermore, aging process solutions, saturated with gypsum, with anhydrite seeds at moderate temperatures (~80°C) would decrease the calcium content, provided that the solution is slightly acidic. |
author2 |
Papangelakis, Vladimiros G. |
author_facet |
Papangelakis, Vladimiros G. Azimi, Ghazal |
author |
Azimi, Ghazal |
author_sort |
Azimi, Ghazal |
title |
Evaluating the Potential of Scaling due to Calcium Compounds in Hydrometallurgical Processes |
title_short |
Evaluating the Potential of Scaling due to Calcium Compounds in Hydrometallurgical Processes |
title_full |
Evaluating the Potential of Scaling due to Calcium Compounds in Hydrometallurgical Processes |
title_fullStr |
Evaluating the Potential of Scaling due to Calcium Compounds in Hydrometallurgical Processes |
title_full_unstemmed |
Evaluating the Potential of Scaling due to Calcium Compounds in Hydrometallurgical Processes |
title_sort |
evaluating the potential of scaling due to calcium compounds in hydrometallurgical processes |
publishDate |
2010 |
url |
http://hdl.handle.net/1807/24672 |
work_keys_str_mv |
AT azimighazal evaluatingthepotentialofscalingduetocalciumcompoundsinhydrometallurgicalprocesses |
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1716611679258673152 |