首页> 美国政府科技报告 >Development Document for Final Effluent Limitations Guidelines and Standards for211 the Pharmaceutical Manufacturing Point Source Category
【24h】

Development Document for Final Effluent Limitations Guidelines and Standards for211 the Pharmaceutical Manufacturing Point Source Category

机译:最终排放限制的发展文件211制药生产点来源类别的指南和标准

获取原文

摘要

;Table of Contents: Introduction; Summary; Industry Description; Industry211u001eSubcategorization; Water Use and Wastewater Characterization; Pollutants Selected 211u001efor Regulation; Description of the Control and Treatment Options; Performance of 211u001ethe Control and Treatment Options; Pollutant Reduction Estimates; Costs of 211u001eTechnology Bases of Regulations; Regulatory Options Selection; Nonwater Quality 211u001eEnvironmental Impacts; Best Practicable Control Technology (BPT); Best 211u001eConventional Technology; Best Available Technology Economically Achievable (BAT); 211u001eNew Source Performance Standards (NSPS); and Pretreatment Standards for Existing 211u001eSources (PSES) and Pretreatment Standards for New Sources (PSNS).

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号