膜生物反应器在制药废水和生物源元素废水净化中的应用前景

M. Boichenko, O. Vovk, S. Boichenko, S. Shamanskyi
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引用次数: 3

摘要

本文分析了生物耐药药品和生物源元素废水的现代处理方法。药品,如抗炎药、镇痛药、抗生素、麻醉药、激素、降胆固醇药物等。,通常少量进入污水中。它们很难被生物降解,经过污水处理厂后没有任何变化,往往最终进入水体。它们即使少量存在于开阔水域,也会对水生生态系统和人类健康产生重大负面影响。在废水中存在的营养物质中,氮和磷化合物最值得关注。当它们进入水体时,会引起富营养化,这对生态系统和人类也很危险。结果表明,在现代各种纯化方法中,最适合去除医药产品和生物源元素的是生化法和光净化技术,以及使用膜生物反应器。生物吸附膜法为利用现代生物技术有效去除生物抗性外源物和减少其对自然环境的负面影响提供了可能性。使用光净化技术可以帮助减少地表水体中排放的营养物质的数量,从而减少其富营养化的可能性,并获得额外的可再生能源。圣经30,图3,表4。
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PERSPECTIVES OF MEMBRANE BIOREACTORS FOR WASTEWATER PURIFICATION FROM WASTE OF PHARMACEUTICAL PRODUCTS AND BIOGENIC ELEMENTS
The article analyzes modern methods of wastewater treatment from bioresistant pharmaceutical products and biogenic elements. Pharmaceuticals, such as anti-inflammatory drugs, analgesics, antibiotics, narcotic drugs, hormones, drugs that reduce cholesterol,etc., are often get into sewage in small quantities. They are hardly biodegradable and, passing through wastewater treatment plants without any changes, they often end up in water bodies. They have significant negative impact on aquatic ecosystems and human health, while being present in open waters even in small quantities. Among the nutrients that are also present in the wastewater, nitrogen and phosphorus compounds deserve the greatest attention. While getting into water bodies, they cause eutrophication, which isalso dangerous to ecosystems and human beings. It is shown that among modern variety of purification methods, the most suitable for removal of pharmaceutical products and biogenic elements are biochemical methods and photopurification technologies, as well as using membrane bioreactors. Biosorption-membrane methods open the possibility to use modern biotechnologies for efficient removal of bioresistant xenobiotics and reducing their negative impact on natural environment. Using photopurification technologies can help to reduce amount of nutrients discharged in surface water bodies, thus reducing their potential for eutrophication, as well as receiving additional renewable energy sources. Bibl. 30, Fig. 3, Tab. 4.  
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