Hu Xuewei, Li Aimin, Fan Jun, Deng Conglin, Zhang Quanxing
State Key Laboratory of Pollution Control and Resources Reuse, School of the Environment, Nanjing University, Nanjing 210093, PR China.
Bioresour Technol. 2008 Jul;99(10):4529-33. doi: 10.1016/j.biortech.2007.08.039. Epub 2007 Oct 22.
This work combined selective adsorption and bioaugmentation to treat mixed wastewater of nitrobenzene and p-nitrophenol. The mixed wastewater of nitrobenzene (217 mg/L) and p-nitrophenol (500 mg/L) was adjusted its pH to 8 and then passed through the adsorption column at 100 mL/h. In effluent the nitrobenzene concentration was less than 4 mg/L. Without the toxic inhibition of nitrobenzene, p-nitrophenol in effluent could be degraded within 60 h through bioaugmentation. About 23 mg/g of nitrobenzene adsorbed the dry resin HU-05 could be desorbed and degraded through bioaugmentation. During this process the adsorption capacity of the resin HU-05 was recovered partly. The recovered extent was limited by nitrobenzene bioavailability. The performance of the resin HU-05 kept stably in the recycle experiments of 60 days.
本研究将选择性吸附与生物强化相结合,用于处理含硝基苯和对硝基苯酚的混合废水。将硝基苯(217mg/L)和对硝基苯酚(500mg/L)的混合废水pH调至8,然后以100mL/h的流速通过吸附柱。流出液中硝基苯浓度低于4mg/L。在没有硝基苯毒性抑制的情况下,流出液中的对硝基苯酚可通过生物强化在60h内降解。干燥树脂HU-05吸附的约23mg/g硝基苯可通过生物强化解吸并降解。在此过程中,树脂HU-05的吸附容量部分得以恢复。恢复程度受硝基苯生物可利用性的限制。在60天的循环实验中,树脂HU-05的性能保持稳定。