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臭氧催化氧化-BAF组合工艺深度处理抗生素制药废水
引用本文:何锦垚, 魏健, 张嘉雯, 刘雪瑜, 宋永会, 杨大壮, 王俭. 臭氧催化氧化-BAF组合工艺深度处理抗生素制药废水[J]. 环境工程学报, 2019, 13(10): 2385-2392. doi: 10.12030/j.cjee.201902043
作者姓名:何锦垚  魏健  张嘉雯  刘雪瑜  宋永会  杨大壮  王俭
作者单位:1.辽宁大学环境学院,沈阳 110036; 2.中国环境科学研究院城市水环境研究室,北京 100012; 3.北京建工环境修复股份有限公司,北京 100015
基金项目:国家自然科学基金;中央级公益性科研院所基本科研业务费专项;中央级公益性科研院所基本科研业务费专项
摘    要:针对抗生素制药废水组分复杂、毒性强、难生物降解的特点,以Ce负载天然沸石作为催化剂(Ce/NZ),采用臭氧催化氧化-曝气生物滤池(BAF)组合工艺对抗生素制药废水二级生化处理出水进行深度处理。结果表明,Ce/NZ催化剂可显著改善臭氧预处理单元的处理效率,在臭氧进气浓度为50 mg·L−1、臭氧进气量为600 mL·min−1、催化剂用量为1 g·L−1、臭氧反应时间为120 min的条件下,臭氧催化氧化预处理对抗生素制药废水的COD去除率达到43%,平均COD由220 mg·L−1降至125 mg·L−1,BOD5/COD由0.12升至0.28,废水的可生化性得到显著提高。臭氧预处理单元出水采用BAF进行生化处理,在进水平均COD为125 mg·L−1、平均NH4+-N为12 mg·L−1、水力停留时间为4 h、气水比为4∶1的条件下,COD和NH4+-N的平均去除率分别为62%和64%。组合工艺处理后出水平均COD和NH4+-N分别为46 mg·L−1和4.1 mg·L−1,出水水质可以稳定达到《发酵类制药工业水污染物排放标准》(GB 21903-2008)。相较于单独BAF工艺,组合工艺出水COD和NH4+-N平均去除率分别提高了66%和15%,出水水质明显优于单独BAF工艺出水。

关 键 词:制药废水   催化   臭氧氧化   曝气生物滤池   深度处理
收稿时间:2019-02-15

Advanced treatment of antibiotic pharmaceutical wastewater by catalytic ozonation combined with BAF process
HE Jinyao, WEI Jian, ZHANG Jiawen, LIU Xueyu, SONG Yonghui, YANG Dazhuang, WANG Jian. Advanced treatment of antibiotic pharmaceutical wastewater by catalytic ozonation combined with BAF process[J]. Chinese Journal of Environmental Engineering, 2019, 13(10): 2385-2392. doi: 10.12030/j.cjee.201902043
Authors:HE Jinyao  WEI Jian  ZHANG Jiawen  LIU Xueyu  SONG Yonghui  YANG Dazhuang  WANG Jian
Affiliation:1.College of Environmental Sciences, Liaoning University, Shenyang 110036, China; 2.Department of Urban Water Environmental Research, Chinese Research Academy of Environmental Sciences, Beijing 100012, China; 3.Beijing Construction Engineering Group Environmental Remediation Co. Ltd., Beijing 100015, China
Abstract:In view of the complex, toxic and difficult biodegradation of antibiotic pharmaceutical wastewater, the Ce-loaded natural zeolite was used as a catalyst (Ce/NZ), and the ozone-catalyzed biological aerated filter (BAF) combination process was applied to advanced treatment of the secondary biochemical treatment effluent of antibiotic pharmaceutical wastewater. The results showed that the Ce/NZ catalyst could significantly improve the treatment efficiency of the ozone pretreatment unit. With the ozone inlet concentration of 50 mg·L−1, the ozone intake of 600 mL·min−1, the catalyst dosage of 1 g·L−1 and the ozone reaction time of 120 min, the COD removal rate of antibiotic pharmaceutical wastewater reached 43%, the average COD value was reduced from 220 mg·L−1 to 125 mg·L−1, and the BOD5/COD increased from 0.12 to 0.28, during which the biodegradability of wastewater was significantly improved. The effluent of the ozone pretreatment unit was biochemically treated by BAF. At average influent COD value of 125 mg·L−1, the average influent ${rm{NH}}_4^{+} $-N concentration of 12 mg·L−1, the hydraulic retention time of 4 h, and the gas to water ratio of 4∶1, the average removal rates of COD and ${rm{NH}}_4^{+} $-N were 62% and 64%, respectively. After the combined process treatment, the average concentrations of COD and ${rm{NH}}_4^{+} $-N in the effluent were 46 mg·L−1 and 4.1 mg·L−1, respectively, and the effluent water quality could stably meet the Discharge Standards of Water pollutants for Pharmaceutical Industry Fermentation Products Category (GB 21903-2008). Compared with the BAF process alone, the average removal rates of COD and ${rm{NH}}_4^{+} $-N in the effluent of combined process increased by 66% and 15%, respectively, and the effluent quality was significantly better than that of the BAF process alone.
Keywords:pharmaceutical wastewater  catalysis  ozonation  biological aerated filter  advanced treatment
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