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Sulfate removal from acid mine water from the deepest active European mine by precipitation and various electrocoagulation configurations.

08:00 EDT 31st August 2018 | BioPortfolio

Summary of "Sulfate removal from acid mine water from the deepest active European mine by precipitation and various electrocoagulation configurations."

Sulfate removal from mine or process water is a key issue in the mining industry. In this paper, precipitation with lime (calcium oxide) was integrated with electrocoagulation for sulfate removal from Pyhäsalmi/Finland mine water. Sulfate precipitation with calcium oxide decreased the sulfate concentration from 13,000 mg/L to 1600 mg/L. Various current densities were applied to the pre-treated mine water with various electrodes and aluminium and iron anodes. It was found that 25 mA/cm was the best tested current density for both anode types. At the second stage, this current density was used for different iron and aluminium anodes in various monopolar and bipolar configurations. It was found that this hybridisation is effective for sulfate removal, and that a bipolar configuration showed better results than the monopolar configuration. The best result was gained from 25 mA/cm with a two aluminium and two stainless steel anode-cathode configuration and calcium oxide pre-treatment to reach pH 12. The removal efficiency reached 84.4% and 63.8% with aluminium anodes in bipolar and monopolar configurations, respectively. This setup was able to decrease sulfate concentrations from 13,000 mg/L to 250 mg/L, which meets mine water discharge limits. Kinetic studies showed that iron and aluminium anodes obey pseudo-second order kinetic. Finally, the energy consumption was calculated.

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This article was published in the following journal.

Name: Journal of environmental management
ISSN: 1095-8630
Pages: 162-171

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Medical and Biotech [MESH] Definitions

An enzyme that specifically cleaves the ester sulfate of iduronic acid. Its deficiency has been demonstrated in Hunter's syndrome, which is characterized by an excess of dermatan sulfate and heparan sulfate. EC 3.1.6.13.

Derivatives of chondroitin which have a sulfate moiety esterified to the galactosamine moiety of chondroitin. Chondroitin sulfate A, or chondroitin 4-sulfate, and chondroitin sulfate C, or chondroitin 6-sulfate, have the sulfate esterified in the 4- and 6-positions, respectively. Chondroitin sulfate B (beta heparin; DERMATAN SULFATE) is a misnomer and this compound is not a true chondroitin sulfate.

5'-Adenylic acid, monoanhydride with sulfuric acid. The initial compound formed by the action of ATP sulfurylase on sulfate ions after sulfate uptake. Synonyms: adenosine sulfatophosphate; APS.

A naturally occurring glycosaminoglycan found mostly in the skin and in connective tissue. It differs from CHONDROITIN SULFATE A (see CHONDROITIN SULFATES) by containing IDURONIC ACID in place of glucuronic acid, its epimer, at carbon atom 5. (from Merck, 12th ed)

An enzyme that catalyzes the activation of sulfate ions by ATP to form adenosine-5'-phosphosulfate and pyrophosphate. This reaction constitutes the first enzymatic step in sulfate utilization following the uptake of sulfate. EC 2.7.7.4.

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