||Analytical methods for the determination of pollutants in pharmaceutical manufacturing industry wastewater.
||Environmental Protection Agency, Washington, DC. Engineering and Analysis Div.
|| U.S. Environmental Protection Agency, Office of Water, Engineering and Analysis Division,
Water--Pollution--United States--Measurement. ;
Pharmaceutical industry--Waste disposal--Environmental aspects--United States.
Water pollution control ;
Test methods ;
Industrial waste treatment ;
Drug industry ;
Chemical analysis ;
Chemical effluents ;
Water pollution sampling ;
Industrial plants ;
Industrial water ;
Point sources ;
Analytical chemistry ;
Mass spectroscopy ;
Organic compounds ;
HPLC(High-pressure liquid chromatography) ;
Volatile organic compounds ;
Semi-volatile organic compounds ;
EPA Method 1665 ;
EPA Method 1666 ;
EPA Method 1667 ;
EPA Method 1671 ;
EPA Method 1673 ;
40 CFR Part 439
||Most EPA libraries have a fiche copy filed under the call number shown. Check with individual libraries about paper copy.
||v, 128 pages : illustrations ; 28 cm
The U.S. Environmental Protection Agency (EPA or the Agency) is proposing effluent limitations guidelines and standards for promulgation at 40 CFR Part 439 for the Pharmaceutical Manufacturing Industrial category to control the discharge of pollutants into surface water of the United States. This compendium of test procedures (methods) supports the proposal. The purpose of publishing the compendium is to provide a single source of methods that are unique to the proposed rule. These methods or the referenced methods must be used for filing permit applications and for compliance monitoring under the National Pollutant Discharge Elimination System (NPDES) program.
Distributed to depository libraries in microfiche. Shipping list no.: 95-0465-M. "February 1995"--Cover. Includes bibliographical references. "EPA 821-B-94-001"--Cover. "This document was prepared under EPA contract no. 68-C3-0337 by the Environmental Programs Division of DynCorp"--Title page verso. Microfiche.