Suppr超能文献

头孢唑林抗生素制剂废水采用臭氧及臭氧/过氧化氢工艺的可处理性

Treatability of cefazolin antibiotic formulation effluent with O3 and O3/H2O2 processes.

作者信息

Iskender G, Sezer A, Arslan-Alaton I, Germirli Babuna F, Okay O S

机构信息

Istanbul Technical University, Civil Engineering Faculty, Environmental Engineering Department, 34469, Maslak, Istanbul, Turkey.

出版信息

Water Sci Technol. 2007;55(10):217-25. doi: 10.2166/wst.2007.325.

Abstract

The effect of applying ozonation and perozonation to antibiotic cefazolin-Na formulation effluents were investigated in this study. Twenty minutes of ozonation at a rate of 1,500 mg/L-h was observed to remove COD by 38%, whereas a COD removal efficiency of 40% was achieved via H2O2 enhanced ozonation (same conditions + 31.25 mM H2O2). Both of the pretreatment alternatives were monitored to elevate the BOD5/COD ratio from 0.01 to 0.08. The initially inert COD was reduced by 38% using ozonation and by 60% employing H2O2 enhanced ozonation. In terms of the lowest achievable effluent COD levels after bio-treatment, ozonation was observed to yield a residual COD of 205 mgL(-1), while a residual COD of 135 mgL(-1) was involved for perozonation. According to the results of acute toxicity on Phaedactylum tricornutum, ozonated and perozonated samples exhibited more toxicity than the untreated effluent after 4 days. The activated sludge inhibition test demonstrated that both of the pretreatment alternatives efficiently eliminated the inhibition of investigated formulation effluent.

摘要

本研究考察了臭氧化和过臭氧化处理抗生素头孢唑林钠制剂废水的效果。在1500mg/L·h的速率下进行20分钟臭氧化处理,观察到化学需氧量(COD)去除率为38%,而通过过氧化氢强化臭氧化(相同条件+31.25mM过氧化氢)实现的COD去除效率为40%。监测这两种预处理方法,以将生化需氧量与化学需氧量(BOD5/COD)的比值从0.01提高到0.08。使用臭氧化处理时,初始惰性COD降低了38%,采用过氧化氢强化臭氧化时降低了60%。就生物处理后可达到的最低出水COD水平而言,观察到臭氧化处理产生的残余COD为205mg/L,而过臭氧化处理的残余COD为135mg/L。根据对三角褐指藻的急性毒性结果,臭氧化和过臭氧化样品在4天后比未处理的废水表现出更大的毒性。活性污泥抑制试验表明,这两种预处理方法都能有效消除所研究制剂废水的抑制作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验