首页> 外文会议>Water Environment Federation 72nd annual conference amp; exposition (WEFTEC'99) >REFINEMENT OF THE EPA'S POTW PASSTHROUGH ANALYSIS METHOD FOR APPLICATION TO THE PHARMACEUTICAL MANUFACTURING INDUSTRY
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REFINEMENT OF THE EPA'S POTW PASSTHROUGH ANALYSIS METHOD FOR APPLICATION TO THE PHARMACEUTICAL MANUFACTURING INDUSTRY

机译:EPA的POTW穿透分析方法的完善,可用于制药业

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The U.S. Environmental Protection Agency (EPA) is required by the Clean Water Actrnto establish industrial pretreatment standards for pollutants that may "pass-through" orrninterfere with publicly owned treatment works (POTW). Through the years EPA hasrnused a pass-through analysis method that compares the percent removals ofrnpollutants by industry plants with treatment that represented best available technologyrneconomically achievable (BAT) to percent removals of the same pollutants by a set ofrnwell designed and operated POTWs. Pass-through is determined if the percentrnremoval of a pollutant by a BAT plant is greater than the percent removal of thatrnpollutant at a POTW. Pass-through is also identified if a pollutant is predicted tornvolatilize in the POTW sewer or treatment units, because this volatilization is notrnconsidered treatment.rnWhen EPA began the revision of the pharmaceutical manufacturing effluentrnlimitations guidelines and standards in 1991, it identified a number of pollutants that itrnhad not regulated in previous rules. A number of these pollutants were oxygenatedrnchemicals such as acetone, methanol, ethanol, and isopropanol. Because thesernchemicals are semi-volatile but also highly soluble and are biodegradable, the POTWrnpass-through methodology was revisited to assure that it would be a technicallydefensiblernapproach for identifying those pollutants requiring pretreatment standards.rnThis paper describes the efforts that were undertaken by EPA, in cooperation with thernPharmaceutical Research and Manufacturers of America (PhRMA), to develop thernnecessary data and information for refining the POTW pass-through methodology forrnuse in the development of the pharmaceutical manufacturing effluent guidelines andrnstandards, which were promulgated on September 21, 1998. This successful effortrnhas resulted in an approach to pass-through analysis that considers multiplernproperties of a chemical, including volatility, solubility, and biodegradability.
机译:《清洁水法》要求美国环境保护局(EPA)为可能“通过”或干扰公有处理厂(POTW)的污染物建立工业预处理标准。多年来,EPA一直采用一种通过分析方法,该方法将经过工厂处理的,代表最佳可经济实现的最佳技术(BAT)的处理工厂的污染物去除百分比与通过一套精心设计和运行的POTW去除相同污染物的百分比进行比较。确定是否通过BAT装置去除污染物的百分比大于在POTW处去除污染物的百分比。如果预测污染物会在POTW下水道或处理单元中挥发掉,也可以确定通过,因为这种挥发没有被考虑处理。当EPA在1991年开始修订制药生产废水限量指南和标准时,它确定了许多污染物以前的规则中没有对此进行监管。其中许多污染物是含氧化合物,例如丙酮,甲醇,乙醇和异丙醇。由于这些化学品是半挥发性的,但也具有很高的溶解性和可生物降解性,因此对POTWrnpass-through方法进行了重新研究,以确保它是鉴定需要预处理标准的那些污染物的技术上可行的方法。本文介绍了EPA在合作下所做的努力与美国药品研究与制造商(PhRMA)合作,开发必要的数据和信息,以完善POTW传递方法,以用于制定制药生产废水准则和标准,该方法于1998年9月21日颁布。一种通过分析的方法,该方法考虑了化学品的多种特性,包括挥发性,溶解性和生物降解性。

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