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35 ARSENIC REMOVAL USING ELECTROCHEMICALLY GENERATED IRON IN CONJUNCTION WITH HYDROGEN PEROXIDE ADDITION Michael D. Brewster, Research Chemist Michael N. Laschinger, Process Engineer Andco Environmental Processes, Inc. Amherst, New York 14228-2380 INTRODUCTION Arsenic is a common contaminant that exhibits varying degrees of toxicity depending on its chemical form. Its potential to form highly toxic compounds, coupled with the fact that arsenic chemistry allows it to form soluble compounds has made arsenic one of the inorganic contaminants regulated in the National Primary Drinking Water Regulations. As of May, 1990, the Environmental Protection Agency (EPA) Maximum Contaminant Level (MCL) allowed for point source discharges is 0.05 milligrams per liter.' Many sources of arsenic contaminated water are required to meet even stricter limits due to state and local regulations. A factor in determining these point source limits is where the discharge is being sent. Surface water discharges regularly have lower limits than discharges to a municipality. It is common to have limits of 0.025 ppm arsenic. There are many sources of arsenic. Naturally occurring arsenide is commonly present in many sulfide ores such as cobalt, copper, lead, silver, tin, and zinc. Arsenic is found in the minerals realgar (AsS) and orpiment (As2S3). These mineral forms are highly insoluble and pose little threat to the environment. The chemistry of arsenic and its presence at trace levels in soils have resulted in arsenic being detected in waters, plant tissues, and animals throughout the world. Levels of natural occurring arsenic seldom pose health risks. Arsenic does have industrial uses. It is commercially produced as a by-product from ores of metals. Arsenic trioxide (As203) is obtained during the smelting process. From this oxide, many other arsenic compounds are produced, notably those used for pesticide and herbicide formulations. Refined arsenic trioxide is also used to decolorize glass and as an ingredient of some pyrotechnics. It is present in some wastewaters from chemical production plants, tannery operations, wood preserving and timber products processing facilities, paint/pigment formulation companies and semiconductor producers. While arsenic occurs naturally in coal, it becomes an industrial source when coal is converted to energy. As a result, power plant fly ash ponds typically contain soluble arsenic compounds. Soluble forms of arsenic are of much greater concern than insoluble arsenic compounds. Their ability to leach through soils and contaminate groundwater is much greater. Nearly all of the hazard associated with arsenic compounds is the result of industrial products or byproducts. This paper addresses and compares the treatment of a range of arsenic contaminated water sources. THE CHEMISTRY OF ARSENIC Arsenic, atomic number 33, is one of the elements located in group VA of the periodic table.2 Within this group, metallic characteristics increase as atomic number increases. Thus, arsenic will be more metallic than phosphorous, which has atomic number 15. A characteristic of metals, in aqueous solutions, is the loss of electrons and resulting formation of cations. This is only observed for the heavier members of this group, which are antimony and bismuth. These two elements can readily lose three electrons to form simple cations. Arsenic will loose electrons to be in the + 3 or +5 states though in aqueous solutions it exists tightly bound to oxygen which results in an anionic form. Arsenic's anionic form is important when discussing the chemistry of arsenic and how it relates to whether or not successful treatment is achieved. Four stable states are known to occur in nature, they are +5, +3, -3, and 0. The + 5 or pentavalem forms are As04'3, HAs04"2 and H2As04"'.3 They will predominate and be stable in oxygen rich water where mild oxidizing conditions are present. These forms of arsenic in its pentavalent state are 46th Purdue Industrial Waste Conference Proceedings, 1992 Lewis Publishers, Inc., Chelsea, Michigan 48118. Printed in U.S.A. 339
Object Description
Purdue Identification Number | ETRIWC199135 |
Title | Arsenic removal using electrochemically generated iron in conjunction with hydrogen peroxide addition |
Author |
Brewster, Michael D. Laschinger, Michael N. |
Date of Original | 1991 |
Conference Title | Proceedings of the 46th Industrial Waste Conference |
Conference Front Matter (copy and paste) | http://e-archives.lib.purdue.edu/u?/engext,42649 |
Extent of Original | p. 339-346 |
Collection Title | Engineering Technical Reports Collection, Purdue University |
Repository | Purdue University Libraries |
Rights Statement | Digital object copyright Purdue University. All rights reserved. |
Language | eng |
Type (DCMI) | text |
Format | JP2 |
Date Digitized | 2009-11-24 |
Capture Device | Fujitsu fi-5650C |
Capture Details | ScandAll 21 |
Resolution | 300 ppi |
Color Depth | 8 bit |
Description
Title | page 339 |
Collection Title | Engineering Technical Reports Collection, Purdue University |
Repository | Purdue University Libraries |
Rights Statement | Digital copyright Purdue University. All rights reserved. |
Language | eng |
Type (DCMI) | text |
Format | JP2 |
Capture Device | Fujitsu fi-5650C |
Capture Details | ScandAll 21 |
Transcript | 35 ARSENIC REMOVAL USING ELECTROCHEMICALLY GENERATED IRON IN CONJUNCTION WITH HYDROGEN PEROXIDE ADDITION Michael D. Brewster, Research Chemist Michael N. Laschinger, Process Engineer Andco Environmental Processes, Inc. Amherst, New York 14228-2380 INTRODUCTION Arsenic is a common contaminant that exhibits varying degrees of toxicity depending on its chemical form. Its potential to form highly toxic compounds, coupled with the fact that arsenic chemistry allows it to form soluble compounds has made arsenic one of the inorganic contaminants regulated in the National Primary Drinking Water Regulations. As of May, 1990, the Environmental Protection Agency (EPA) Maximum Contaminant Level (MCL) allowed for point source discharges is 0.05 milligrams per liter.' Many sources of arsenic contaminated water are required to meet even stricter limits due to state and local regulations. A factor in determining these point source limits is where the discharge is being sent. Surface water discharges regularly have lower limits than discharges to a municipality. It is common to have limits of 0.025 ppm arsenic. There are many sources of arsenic. Naturally occurring arsenide is commonly present in many sulfide ores such as cobalt, copper, lead, silver, tin, and zinc. Arsenic is found in the minerals realgar (AsS) and orpiment (As2S3). These mineral forms are highly insoluble and pose little threat to the environment. The chemistry of arsenic and its presence at trace levels in soils have resulted in arsenic being detected in waters, plant tissues, and animals throughout the world. Levels of natural occurring arsenic seldom pose health risks. Arsenic does have industrial uses. It is commercially produced as a by-product from ores of metals. Arsenic trioxide (As203) is obtained during the smelting process. From this oxide, many other arsenic compounds are produced, notably those used for pesticide and herbicide formulations. Refined arsenic trioxide is also used to decolorize glass and as an ingredient of some pyrotechnics. It is present in some wastewaters from chemical production plants, tannery operations, wood preserving and timber products processing facilities, paint/pigment formulation companies and semiconductor producers. While arsenic occurs naturally in coal, it becomes an industrial source when coal is converted to energy. As a result, power plant fly ash ponds typically contain soluble arsenic compounds. Soluble forms of arsenic are of much greater concern than insoluble arsenic compounds. Their ability to leach through soils and contaminate groundwater is much greater. Nearly all of the hazard associated with arsenic compounds is the result of industrial products or byproducts. This paper addresses and compares the treatment of a range of arsenic contaminated water sources. THE CHEMISTRY OF ARSENIC Arsenic, atomic number 33, is one of the elements located in group VA of the periodic table.2 Within this group, metallic characteristics increase as atomic number increases. Thus, arsenic will be more metallic than phosphorous, which has atomic number 15. A characteristic of metals, in aqueous solutions, is the loss of electrons and resulting formation of cations. This is only observed for the heavier members of this group, which are antimony and bismuth. These two elements can readily lose three electrons to form simple cations. Arsenic will loose electrons to be in the + 3 or +5 states though in aqueous solutions it exists tightly bound to oxygen which results in an anionic form. Arsenic's anionic form is important when discussing the chemistry of arsenic and how it relates to whether or not successful treatment is achieved. Four stable states are known to occur in nature, they are +5, +3, -3, and 0. The + 5 or pentavalem forms are As04'3, HAs04"2 and H2As04"'.3 They will predominate and be stable in oxygen rich water where mild oxidizing conditions are present. These forms of arsenic in its pentavalent state are 46th Purdue Industrial Waste Conference Proceedings, 1992 Lewis Publishers, Inc., Chelsea, Michigan 48118. Printed in U.S.A. 339 |
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Color Depth | 8 bit |
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