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DISTRIBUTION OF CADMIUM AND NICKEL IN ACTIVATED SLUDGE SYSTEMS Prasad S. Kodukula, Instructor James W. Patterson, Professor Department of Environmental Engineering Illinois Institute of Technology Chicago, Illinois 60616 INTRODUCTION In recent years, there has been considerable interest in the topic of heavy metals in sewage treatment plants with numerous studies being reported in the literature on their source, fate, effect, and control [1-8]. Whereas several investigators have attempted to characterize adsorption of metals to well-defined oxide surfaces [9-14] and, more recently, to estuarine particulate matter [15], there seems to be a relative lack of information on fundamental aspects of adsorption processes controlling the removals of heavy metals in activated sludge systems. An understanding of the fate of heavy metals in the activated sludge treatment system requires characterization of metal distribution in terms of the various physical, chemical, and biological interactions during each stage of the treatment. The extent and affinity of such interactions is a complex function of intrinsic variables, such as, the individual metal, its concentration, and presence of other metals; the physical-chemical characteristics of the aqueous medium, such as, temperature, solids content, pH, alkalinity and complexing ligands; and operational factors, including solids retention time. Among the mechanisms which are reported to affect the metal distribution between the soluble and solid phases in an activated sludge system are: adsorption, complexation, ion-exchange, precipitation, and biological uptake. Several investigators [16,17] have concluded that biological uptake metals is rather slow and insignificant compared to the physical-chemical mechanisms influencing the metals distribution. Whereas Jenkins et al. [18,19] attributed the observed metals removals in raw sewage and digested sludge primarily to precipitation, most investigators in recent years have assumed that precipitation is insignificant in their studies involving adsorption in activated sludge mixed liquor [17,20]. However, Brown and Lester [21] recently suggested that both precipitation and adsorption of metals have taken place in their batch cultures of K. aerogenes. an organism commonly found in activated sludge. A thorough evaluation of experimental procedures and results reported in the literature pertaining to the characterization of metal adsorption processes and description of these processes by isotherm models raises several interesting questions, which need to be answered for a better understanding of the adsorption process in activated sludge systems: Is the assumption that the test liquid is in equilibrium (forward adsorption rate = backward desorption rate) with metal after a few hours of contact time valid? How do pH and concentration of total metal and suspended solids affect the adsorption behavior of metals? Is precipitation a significant factor affecting the distribution of metals? This investigation makes an attempt to answer these questions. CONCEPTUAL MODEL In order to be able to characterize the adsorption process and its relation with precipitation in solid-liquid suspensions, a conceptual model is proposed here, as described below. 439
Object Description
Purdue Identification Number | ETRIWC198346 |
Title | Distribution of cadmium and nickel in activated sludge systems |
Author |
Kodukula, Prasad S. Patterson, James William, 1940- |
Date of Original | 1983 |
Conference Title | Proceedings of the 38th Industrial Waste Conference |
Conference Front Matter (copy and paste) | http://e-archives.lib.purdue.edu/u?/engext,34749 |
Extent of Original | p. 439-448 |
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 | 2009-07-28 |
Capture Device | Fujitsu fi-5650C |
Capture Details | ScandAll 21 |
Resolution | 300 ppi |
Color Depth | 8 bit |
Description
Title | page 439 |
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 | DISTRIBUTION OF CADMIUM AND NICKEL IN ACTIVATED SLUDGE SYSTEMS Prasad S. Kodukula, Instructor James W. Patterson, Professor Department of Environmental Engineering Illinois Institute of Technology Chicago, Illinois 60616 INTRODUCTION In recent years, there has been considerable interest in the topic of heavy metals in sewage treatment plants with numerous studies being reported in the literature on their source, fate, effect, and control [1-8]. Whereas several investigators have attempted to characterize adsorption of metals to well-defined oxide surfaces [9-14] and, more recently, to estuarine particulate matter [15], there seems to be a relative lack of information on fundamental aspects of adsorption processes controlling the removals of heavy metals in activated sludge systems. An understanding of the fate of heavy metals in the activated sludge treatment system requires characterization of metal distribution in terms of the various physical, chemical, and biological interactions during each stage of the treatment. The extent and affinity of such interactions is a complex function of intrinsic variables, such as, the individual metal, its concentration, and presence of other metals; the physical-chemical characteristics of the aqueous medium, such as, temperature, solids content, pH, alkalinity and complexing ligands; and operational factors, including solids retention time. Among the mechanisms which are reported to affect the metal distribution between the soluble and solid phases in an activated sludge system are: adsorption, complexation, ion-exchange, precipitation, and biological uptake. Several investigators [16,17] have concluded that biological uptake metals is rather slow and insignificant compared to the physical-chemical mechanisms influencing the metals distribution. Whereas Jenkins et al. [18,19] attributed the observed metals removals in raw sewage and digested sludge primarily to precipitation, most investigators in recent years have assumed that precipitation is insignificant in their studies involving adsorption in activated sludge mixed liquor [17,20]. However, Brown and Lester [21] recently suggested that both precipitation and adsorption of metals have taken place in their batch cultures of K. aerogenes. an organism commonly found in activated sludge. A thorough evaluation of experimental procedures and results reported in the literature pertaining to the characterization of metal adsorption processes and description of these processes by isotherm models raises several interesting questions, which need to be answered for a better understanding of the adsorption process in activated sludge systems: Is the assumption that the test liquid is in equilibrium (forward adsorption rate = backward desorption rate) with metal after a few hours of contact time valid? How do pH and concentration of total metal and suspended solids affect the adsorption behavior of metals? Is precipitation a significant factor affecting the distribution of metals? This investigation makes an attempt to answer these questions. CONCEPTUAL MODEL In order to be able to characterize the adsorption process and its relation with precipitation in solid-liquid suspensions, a conceptual model is proposed here, as described below. 439 |
Resolution | 300 ppi |
Color Depth | 8 bit |
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