Oxidation Kinetics of Pyrite in Synthetic Seawater

Oxidation Kinetics of Pyrite in Synthetic Seawater PDF Author: Taylor Alexander van Hoorebeke
Publisher:
ISBN: 9781369656565
Category : Ocean bottom
Languages : en
Pages : 87

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Book Description
As the demand for industrial materials rises, mining companies have become increasingly interested in exploiting unconventional metal resources. Seafloor massive sulfide (SMS) deposits, one such example of an unconventional resource, will be mined for their high ore grade and abundance along oceanic plate margins. As these deposits are mined, fresh and highly reactive surfaces of sulfide minerals will be exposed to seawater, causing them to immediately oxidize. Pyrite (FeS2) is the most common sulfide mineral and readily oxidizes under atmospheric conditions. Sulfuric acid is a product of the sulfide mineral oxidation process and is often responsible for the devastating effects of acid mine drainage at terrestrial mining sites. Kinetics experiments have been conducted to determine a rate law for the abiotic rate of pyrite oxidation in synthetic seawater. Experiments run from pH 2-5, 0.995 or 0.10 atm O2, and temperatures of 285 - 303 K were used in rate law calculations. The experimentally derived molal specific rate law is: Rsp = -10-11.02±0.03[H+]0.39±0.03[PO2]0.44±0.05 where [H+] and [PO2] represent the initial molal concentrations of protons and dissolved oxygen in the seawater, and the rate Rsp is in units of moles m-2 sec-1. The initial rate method was combined with the method of isolation to determine the effects that pH, dissolved oxygen concentration, and temperature have on the pyrite oxidation rate. Results show that the initial concentration of dissolved oxygen is more influential upon the initial pyrite oxidation rate than the initial pH of the seawater under acidic, low temperature conditions. The pyrite oxidation rate in acidic seawater is the slowest of the sulfides pyrite, pyrrhotite, and chalcopyrite, with the reaction proceeding up to three orders of magnitude slower than that of pyrrhotite in synthetic seawater. The slow pyrite weathering rate (whether natural or anthropogenically induced) enhanced pyrite preservation in massive sulfide deposits. This may explain why VMS deposits are more enriched in pyrite than any other sulfide mineral.

Oxidation Kinetics of Pyrite in Synthetic Seawater

Oxidation Kinetics of Pyrite in Synthetic Seawater PDF Author: Taylor Alexander van Hoorebeke
Publisher:
ISBN: 9781369656565
Category : Ocean bottom
Languages : en
Pages : 87

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Book Description
As the demand for industrial materials rises, mining companies have become increasingly interested in exploiting unconventional metal resources. Seafloor massive sulfide (SMS) deposits, one such example of an unconventional resource, will be mined for their high ore grade and abundance along oceanic plate margins. As these deposits are mined, fresh and highly reactive surfaces of sulfide minerals will be exposed to seawater, causing them to immediately oxidize. Pyrite (FeS2) is the most common sulfide mineral and readily oxidizes under atmospheric conditions. Sulfuric acid is a product of the sulfide mineral oxidation process and is often responsible for the devastating effects of acid mine drainage at terrestrial mining sites. Kinetics experiments have been conducted to determine a rate law for the abiotic rate of pyrite oxidation in synthetic seawater. Experiments run from pH 2-5, 0.995 or 0.10 atm O2, and temperatures of 285 - 303 K were used in rate law calculations. The experimentally derived molal specific rate law is: Rsp = -10-11.02±0.03[H+]0.39±0.03[PO2]0.44±0.05 where [H+] and [PO2] represent the initial molal concentrations of protons and dissolved oxygen in the seawater, and the rate Rsp is in units of moles m-2 sec-1. The initial rate method was combined with the method of isolation to determine the effects that pH, dissolved oxygen concentration, and temperature have on the pyrite oxidation rate. Results show that the initial concentration of dissolved oxygen is more influential upon the initial pyrite oxidation rate than the initial pH of the seawater under acidic, low temperature conditions. The pyrite oxidation rate in acidic seawater is the slowest of the sulfides pyrite, pyrrhotite, and chalcopyrite, with the reaction proceeding up to three orders of magnitude slower than that of pyrrhotite in synthetic seawater. The slow pyrite weathering rate (whether natural or anthropogenically induced) enhanced pyrite preservation in massive sulfide deposits. This may explain why VMS deposits are more enriched in pyrite than any other sulfide mineral.

Pyrite Oxidation and Its Control

Pyrite Oxidation and Its Control PDF Author: V. P. Evangelou
Publisher: CRC Press
ISBN: 1351420798
Category : Science
Languages : en
Pages : 308

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Book Description
Pyrite Oxidation and its Control is the single available text on the market that presents the latest findings on pyrite oxidation and acid mine drainage (AMD). This new information is an indispensable reference for generating new concepts and technologies for controlling pyrite oxidation. This book focuses on pyrite oxidation theory, experimental findings on oxidation mechanisms, as well as applications and limitations of amelioration technologies. The text also includes discussions on the theory and potential application of novel pyrite microencapsulation technologies for controlling pyrite oxidation currently under investigation in the author's laboratory.

The Kinetics of Pyrite Oxidation in Marine Systems

The Kinetics of Pyrite Oxidation in Marine Systems PDF Author: Teresa Ann Hood
Publisher:
ISBN:
Category :
Languages : en
Pages : 238

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Kinetics of Pyrite Oxidation

Kinetics of Pyrite Oxidation PDF Author: Americo Luis Larez
Publisher:
ISBN:
Category : Oxidation
Languages : en
Pages : 80

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Kinetics and Mechanisms of Pyrite (FeS2) Oxidation in the Formation of Acid Mine Drainage

Kinetics and Mechanisms of Pyrite (FeS2) Oxidation in the Formation of Acid Mine Drainage PDF Author: Abbas Hussain Mirza
Publisher:
ISBN:
Category :
Languages : en
Pages : 548

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Kinetics of Aqueous Pyrite Oxidation by Dissolved Oxygen from PH 3.8-5.2 and 10-30 0C

Kinetics of Aqueous Pyrite Oxidation by Dissolved Oxygen from PH 3.8-5.2 and 10-30 0C PDF Author: Joseph Diamadi
Publisher:
ISBN:
Category : Oxidation
Languages : en
Pages : 184

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Kinetics of Pyrite Oxidation

Kinetics of Pyrite Oxidation PDF Author: Michael George Paschka
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

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Marine Geochemistry

Marine Geochemistry PDF Author: Horst D. Schulz
Publisher: Springer Science & Business Media
ISBN: 3540321446
Category : Science
Languages : en
Pages : 583

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Book Description
Since 1980 a considerable amount of scientific research dealing with geochemical processes in marine sediments has been carried out. This textbook summarizes the state-of-the-art in this field of research providing a complete representation of the subject and including the most recent findings. The topics covered include the examination of sedimentological and physical properties of the sedimentary solid phase. A new chapter describes properties, occurrence and formation of gas hydrates in marine sediments. The textbook ends with a chapter on model conceptions and computer models to quantify processes of early diagenesis.

The Effect of Alkalinity on the Kinetics of Pyrite Oxidation

The Effect of Alkalinity on the Kinetics of Pyrite Oxidation PDF Author: Jeremy Jon Picard
Publisher:
ISBN:
Category :
Languages : en
Pages : 192

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Chemistry of Marine Water and Sediments

Chemistry of Marine Water and Sediments PDF Author: Antonio Gianguzza
Publisher: Springer Science & Business Media
ISBN: 366204935X
Category : Science
Languages : en
Pages : 513

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Book Description
The most important processes on the Earth`s surface occur in the Ocean where materials and energy are primarily exchanged. In the case of marine chemistry different fields of chemistry from organic to inorganic as well as thermodynamics and biochemistry are involved. Analytical Chemistry is a very important tool for the quantification of biogeochemical processes by providing correct and even more sophisticated methodologies. These are often directly applied 'in situ', in order to detect trace and ultra-trace natural and anthropogenic substances. Kinetic and thermodynamic studies allow us to establish whether the process occurs. Once discovered it is then possible to build up general models for environmental systems. This book gathers many aspects with the aim of creating a general picture of the chemical processes occurring in the marine environment