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Release of arsenic from cyanidation tailings
Luleå University of Technology, Department of Civil, Environmental and Natural Resources Engineering, Geosciences and Environmental Engineering.ORCID iD: 0000-0002-5010-4815
Luleå University of Technology, Department of Civil, Environmental and Natural Resources Engineering, Geosciences and Environmental Engineering.ORCID iD: 0000-0001-9846-1793
Luleå University of Technology, Department of Civil, Environmental and Natural Resources Engineering, Geosciences and Environmental Engineering.ORCID iD: 0000-0001-7585-4017
Luleå University of Technology, Department of Civil, Environmental and Natural Resources Engineering, Geosciences and Environmental Engineering.ORCID iD: 0000-0001-7291-8585
2016 (English)In: Minerals Engineering, ISSN 0892-6875, E-ISSN 1872-9444, Vol. 93, p. 57-64Article in journal (Refereed) Published
Abstract [en]

At a gold mine in northern Sweden, gold occurring as inclusions in pyrrhotite and arsenopyrite is leached by cyanidation of the ore. The main sulphide minerals in the ore are pyrrhotite and arsenopyrite. Effluents from the cyanidation process are treated with Fe2(SO4)3 to form Fe-precipitates suitable for the co-precipitation of As. The aim of this study was to perform static and kinetic leaching tests on the ore and tailings to define geochemical processes governing As mobility. Sequential leaching tests suggested that the majority of dissolved As deriving from the sulphide fraction in the ore was incorporated in newly formed Fe-precipitates in the tailings. The mobility of As in the tailings was therefore mainly dependent on the stability of these As-bearing Fe-precipitates. Weathering cell tests (WCT) involving 31 weekly cycles of wetting and air exposure were conducted to assess the stability of the As in the tailings under accelerated weathering conditions. The first stage of the WCT was characterized by a pH ≈ 5 and low As leaching, probably driven by the dissolution of amorphous Fe-As species. In the second stage of the WCT, leaching of Fe, S and As increased and the pH decreased to <3.5. An increase of the leachate’s molar Fe/S-ratio suggested that pyrrhotite oxidation was occurring. The falling pH destabilized As-bearing Fe-precipitates, causing further As release. The total As release during the WCT corresponded to only a small proportion of the tailings’ total As content. The accelerated As-leaching observed towards the end of the WCT could thus indicate that its release could increase progressively over time.

Place, publisher, year, edition, pages
2016. Vol. 93, p. 57-64
National Category
Geochemistry Geology
Research subject
Tillämpad geokemi; Ore Geology
Identifiers
URN: urn:nbn:se:ltu:diva-5851DOI: 10.1016/j.mineng.2016.04.013ISI: 000377313900008Scopus ID: 2-s2.0-84964596057Local ID: 409d1fb8-7260-414b-88b4-4904aadd11f9OAI: oai:DiVA.org:ltu-5851DiVA, id: diva2:978727
Note
Validerad; 2016; Nivå 2; 20160502 (andbra)Available from: 2016-09-29 Created: 2016-09-29 Last updated: 2018-07-10Bibliographically approved
In thesis
1. Cementation of cyanidation tailings – effects on the release of As, Cu, Ni and Zn
Open this publication in new window or tab >>Cementation of cyanidation tailings – effects on the release of As, Cu, Ni and Zn
2018 (English)Doctoral thesis, comprehensive summary (Other academic)
Alternative title[sv]
Solidifiering av anrikningssand från cyanidlakning – effekter på lakning av arsenik, nickel, zink och koppar
Abstract [en]

Knowledge about mineralogy and chemical composition in sulfidic tailings is essential to predict how tailings management may affect the future leachate quality. At a gold mine in the north of Sweden, gold was extracted from inclusions in arsenopyrite and pyrrhotite by the use of cyanide. Sulfides in the ore dissolved to a large extent during the cyanide leaching process causing sulfide-related elements such as As, Cu, Ni and Zn to be mobilized to a various extent. In a subsequent water treatment process, a significant proportion of As and Cu was captured in secondary formed Fe-precipitates. Large proportions of water-soluble Ni- and Zn-species in tailings suggested that this treatment was insufficient to reduce the mobility of Ni and Zn. Maintaining oxidized, neutral conditions is of major importance for the immobility of As, Cu, Ni and Zn during further management of the cyanidation tailings (CT).

Part of the CT were planned to be managed in underground cavities by the use of a cemented paste backfill (CPB) -application. In CPB, a monolithic mass is formed as tailings are mixed with small proportions (4-7 weight %) of pozzolanic materials and backfilled into underground excavated areas. Using a CPB-application may decrease the sulphide oxidation rate, reducing exposure of mineral surfaces to oxygen and increasing water saturation levels within the material. In this study, CT was mixed with binders (1-3 wt. %) for the formation of a low-strength (0.2 Mpa) CT-CPB-mass. These mixtures were stored at moisturized conditions and subsequently subjected to oxidized and flooded conditions in a laboratory-based study. During short-term storing, high water saturation levels were preserved in the CT-CPB-mixtures, but, sulfide oxidation still progressed, and the release of Zn, Cu, and Ni was still lower compared to that in CT. The opposite was true for As, probably due to a desorption from Fe-precipitates. The desorbed As was subsequently incorporated into less acid-tolerant species (i.e. Ca-arsenates and As bonded to cementitious phases) in the CT-CPB:s, that readily dissolved and released more As compared to that in CT.

A complete flooding of CPB-filled workings may take a long time to be reached. During this transition period, zones with low levels of water saturation forms in the CPB-monoliths, which could increase the sulphide oxidation rate, lower pH and dissolve the cementitious binders. In this study, strength decreased along with the water saturation levels in the CPB-mixtures, due to a more extensive pyrrhotite oxidation. A minimal proportion (1 wt. %) of binders did not suppress Cu and As leaching during flooding, but Ni and Zn-leaching were still lower than from CT. In the CT-CPB:s, proportions of As, Cu, Ni and Zn associated with cementitious phases increased in tandem with the fraction of binders. Using higher binder proportions in the CPB, as water saturation levels were lowered, substantially increased the Zn-release while there was an insignificant change in the As-release, and substantially lower Cu- and Ni-release. Pyrrhotite oxidation proceeded in the CT-CPB-mixtures independent of water saturation level. So, increasing binder proportion in a CPB does not necessary mean that trace metals are more stabilized, due to the formation of acid-intolerant fractions. Results from this study, pinpoints the importance of having knowledge about trace element distribution and mineral assemblage in tailings before management methods are chosen and implemented.

Place, publisher, year, edition, pages
Luleå: Luleå University of Technology, 2018. p. 35
Series
Doctoral thesis / Luleå University of Technology 1 jan 1997 → …, ISSN 1402-1544
National Category
Geochemistry
Research subject
Applied Geochemistry
Identifiers
urn:nbn:se:ltu:diva-68436 (URN)978-91-7790-124-2 (ISBN)978-91-7790-125-9 (ISBN)
Public defence
2018-06-15, E246, Luleå, 09:00 (Swedish)
Opponent
Supervisors
Available from: 2018-04-23 Created: 2018-04-20 Last updated: 2018-05-29Bibliographically approved

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Hamberg, RogerBark, GlennMaurice, ChristianAlakangas, Lena

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