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"■-&* I f ENHANCED COD REMOVAL FROM PHARMACEUTICAL WASTEWATER USING POWDERED ACTIVATED CARBON ADDITION TO AN ACTIVATED SLUDGE SYSTEM Richard A. Osantowski, Manager Industrial Waste Section EnviroEnergy Technology Center Rexnord, Inc. Milwaukee, Wisconsin 53201 Clyde R. Dempsey, Acting Chief Chemicals and Chemical Products Branch Kenneth A. Dostal, Environmental Engineer U.S. Environmental Protection Agency Cincinnati, Ohio 45268 INTRODUCTION The pharmaceutical manufacturing point source category manufactures biological products, medicinal chemicals, botanical products, and pharmaceutical products covered by Standard Industrial Classification Code Numbers 2831, 2833, and 2834, as well as other commodities. The industry is characterized by diversity of product, process, plant size, as well as wastewater quantity and quality. For example, many plants will generate wastewaters with chemical oxygen demand (COD) concentrations ranging from 500 to 1500 mg/l whereas wastewaters from Subcategories A (Fermentation Products) and C (Chemical Synthesis Products) may have COD concentrations up to 10,000 mg/l and higher [1]. These latter plants may be able to discharge treated wastewaters meeting Best Practicable Control Technology Currently Available (BPT), which is defined as a COD removal of 14% [1). However, these treated wastewaters may still contain COD concentrations of 2,600 mg/l and higher. On November 26, 1982, the U.S. Environmental Protection Agency (EPA) proposed Best Available Technology Economically Achievable (BAT) and New Source Performance Standards (NSPS) designed to control the discharge of the nonconventional pollutant, COD, as well as other pollutants from pharmaceutical manufacturing facilities 12,3]. The industry commented that the proposed regulations could not be met by A and C subcategory plants based on the proposed technology. On October 27, 1983, the EPA promulgated final Pharmaceutical Manufacturing Point Source Category Effluent Limitations Guidelines, Pretreatment Standards, and New Source Performance Standards [4,5]. In this rulemaking, the Agency decided to return to the 1976 BPT subcategorization scheme, and, as a result, the 1982 proposed COD regulations are no longer a valid point of comparison. A final decision on appropriate BAT limitations and NSPS for COD was postponed until additional information could be obtained on applicable COD removal technologies and their achievable concentrations. By way of responding to these additional information needs, the EPA initiated a program which included studies designed to evaluate the ability of activated carbon adsorption technologies to reduce the effluent COD concentrations. Two technologies were evaluated at a Subcategories A and C pharmaceutical manufacturing plant which employed secondary treatment and reported high COD concentrations in their discharge monitoring report. The two technologies were: 1) Powdered activated carbon (PAC) addition to the activated-sludge aeration basin; and 2) granular activated carbon (GAC) treatment of the secondary effluent. This paper presents the results of the PAC/activated sludge studies. From September to December, 1984, an eighty-three (83) day study was conducted using the biological pilot plant shown on 719
Object Description
Purdue Identification Number | ETRIWC198572 |
Title | Enhanced COD removal from pharmaceutical wastewater using powdered activated carbon addition to an activated sludge system |
Author |
Osantowski, Richard Dempsey, Clyde R. Dostal, Kenneth A. |
Date of Original | 1985 |
Conference Title | Proceedings of the 40th Industrial Waste Conference |
Conference Front Matter (copy and paste) | http://e-archives.lib.purdue.edu/u?/engext,36131 |
Extent of Original | p. 719-728 |
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 | 2009-07-15 |
Capture Device | Fujitsu fi-5650C |
Capture Details | ScandAll 21 |
Resolution | 300 ppi |
Color Depth | 8 bit |
Description
Title | page 719 |
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 | "■-&* I f ENHANCED COD REMOVAL FROM PHARMACEUTICAL WASTEWATER USING POWDERED ACTIVATED CARBON ADDITION TO AN ACTIVATED SLUDGE SYSTEM Richard A. Osantowski, Manager Industrial Waste Section EnviroEnergy Technology Center Rexnord, Inc. Milwaukee, Wisconsin 53201 Clyde R. Dempsey, Acting Chief Chemicals and Chemical Products Branch Kenneth A. Dostal, Environmental Engineer U.S. Environmental Protection Agency Cincinnati, Ohio 45268 INTRODUCTION The pharmaceutical manufacturing point source category manufactures biological products, medicinal chemicals, botanical products, and pharmaceutical products covered by Standard Industrial Classification Code Numbers 2831, 2833, and 2834, as well as other commodities. The industry is characterized by diversity of product, process, plant size, as well as wastewater quantity and quality. For example, many plants will generate wastewaters with chemical oxygen demand (COD) concentrations ranging from 500 to 1500 mg/l whereas wastewaters from Subcategories A (Fermentation Products) and C (Chemical Synthesis Products) may have COD concentrations up to 10,000 mg/l and higher [1]. These latter plants may be able to discharge treated wastewaters meeting Best Practicable Control Technology Currently Available (BPT), which is defined as a COD removal of 14% [1). However, these treated wastewaters may still contain COD concentrations of 2,600 mg/l and higher. On November 26, 1982, the U.S. Environmental Protection Agency (EPA) proposed Best Available Technology Economically Achievable (BAT) and New Source Performance Standards (NSPS) designed to control the discharge of the nonconventional pollutant, COD, as well as other pollutants from pharmaceutical manufacturing facilities 12,3]. The industry commented that the proposed regulations could not be met by A and C subcategory plants based on the proposed technology. On October 27, 1983, the EPA promulgated final Pharmaceutical Manufacturing Point Source Category Effluent Limitations Guidelines, Pretreatment Standards, and New Source Performance Standards [4,5]. In this rulemaking, the Agency decided to return to the 1976 BPT subcategorization scheme, and, as a result, the 1982 proposed COD regulations are no longer a valid point of comparison. A final decision on appropriate BAT limitations and NSPS for COD was postponed until additional information could be obtained on applicable COD removal technologies and their achievable concentrations. By way of responding to these additional information needs, the EPA initiated a program which included studies designed to evaluate the ability of activated carbon adsorption technologies to reduce the effluent COD concentrations. Two technologies were evaluated at a Subcategories A and C pharmaceutical manufacturing plant which employed secondary treatment and reported high COD concentrations in their discharge monitoring report. The two technologies were: 1) Powdered activated carbon (PAC) addition to the activated-sludge aeration basin; and 2) granular activated carbon (GAC) treatment of the secondary effluent. This paper presents the results of the PAC/activated sludge studies. From September to December, 1984, an eighty-three (83) day study was conducted using the biological pilot plant shown on 719 |
Resolution | 300 ppi |
Color Depth | 8 bit |
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