含碳纳米TiO2光催化降解甲醇

采用管式光催化反应器，在石英玻璃管壁上涂镀含碳纳米TiO2薄膜，研究含碳纳米TiO2对甲醇气体的光催化降解性能。实验结果表明：随气体流量增加，甲醇降解率呈线性降低；在气体流量为200mL／min、相对湿度为40％、甲醇初始质量浓度为90～170mg／m^3的较佳条件下，甲醇降解率维持在80％以上，最高达85％；在甲醇初始质量浓度为150mg／m^3、气体流餐为200mL／min、相对湿度为40％的条件下，德国Degusa—P25光催化剂对甲醇的平均降解率为89％，含碳纳米TiO2对甲醇的平均降解率为82％，最人降解率为85％。     

采用两段SBR工艺处理石化废水

采用两段序批式活性污泥反应器（SBR）工艺处理高浓度石化废水，考察了DO、MLSS、反应温度对废水处理效果的影响。实验结果表明，两段SBR系统中有机物降解存在着不同的作用机理，第一段主要以去除易降解有机物为主，第二段主要以去除难降解有机物为主。在进水COD为4000mg／L、SBR1中DO为4～5mg／L、MLSS为5000mg／L，SBR2中DO为2～4mg／L、MLSS为3000mg／L、反应温度约为20℃的条件下，废水COD去除率达90％以上。     

超临界水氧化处理高浓度丙烯酸废水

采用超临界水氧化（SCWO）技术在连续蒸发壁式反应器内处理高浓度丙烯酸废水。实验结果表明：SCWO能有效地处理丙烯酸废水，废水COD和TOC去除率分别达到99％左右，且反应时间短；反应温度、反应压力和氧化剂加入量的增加有利于COD和TOC去除率的提高。实验得出的废水处理最佳工艺条件：反应温度693K、反应压力24～26MPa、氧化剂加入量1．0～1．5倍。对反应器出口试样进行色谱-质谱联用分析结果表明，小分子醇、醚类以及CO2和CO是主要的液相产物和气相产物。针对腐蚀和盐沉积问题，提出了预防措施。     

IC反应器处理制浆洗草废水的内循环状况

中试用内循环厌氧反应器处理制浆造纸厂的洗草废水,并探讨内循环系统的循环状况。试验表明,洗草水不适合进行深度厌氧处理,宜进行水解酸化。由于洗草废水的有机物浓度低,产气量小,反应器内循环系统仅产生了不连续的提升,液体提升量与产气量的比值在0.08~0.36,下降管中产生了间歇性回流,液体的流量达到了518.4~725.1 L/h。     

滤料粒径对BAF小尺度下流场形态及挂膜速度的影响

为探讨颗粒粒径对曝气生物滤池(BAF)运行效果的影响,采用数值模拟和实验研究方法分析了滤料粒径对曝气生物滤池流场形态及挂膜速度的作用机理.选用5个颗粒尺寸结构空间作为计算区域,利用Fluent软件对相同颗粒间隙、不同颗粒粒径下BAF小尺度下的流场形态进行模拟分析,并通过对3种粒径下流线图、速度矢量图、压力分布及湍流强度变化的对比分析,发现颗粒粒径为3 mm时流场形态最好,最有利于气水混合及氧传质的进行.同时,为验证模拟结果的正确性,对同种材质、相同运行条件下3种不同颗粒粒径进行挂膜速度对比,通过考察挂膜启动28 d的COD去除率变化及污泥生物量的对比分析,发现颗粒粒径为3 mm时,运行最为稳定,系统运行第16 d时就达到了80%的COD去除效率.     

内循环厌氧反应器流动模型及反应过程模拟

为揭示内循环厌氧反应器放大过程中所出现的规律,本文对反应器中流动模型和反应过程进行了模拟研究,通过对主反应区的停留时间分布的实验研究,确定了主反应区流型可用一平推流与两个并联的全混流进行串联的三参数组合模型进行模拟.在实验范围内,平推流区所占的体积分数约为36%,两个全混流区所占的体积分数分别为53%和11%.结合厌氧反应动力学方程,应用组合模型模拟了实际反应器的状态,并和实验值进行了对比,发现反应器出口处CH_4体积流量最大误差为9.67%,在可允许的范围内.同时,模拟了基质初始COD和温度变化对反应器出口状态的影响.研究表明,与其它模型相比,组合模型计算简洁,同时又有较好的精度,能够满足反应器的设计需要.     

Biological removal of antiandrogenic activity in gray wastewater and coking wastewater by membrane reactor process

A recombinant human androgen receptor yeast assay was applied to investigate the occurrence of antiandrogens as well as the mechanism for their removal during gray wastewater and coking wastewater treatment. The membrane reactor (MBR) system for gray wastewater treatment could remove 88.0% of antiandrogenic activity exerted by weakly polar extracts and 97.3% of that by moderately strong polar extracts, but only 32.5% of that contributed by strong polar extracts. Biodegradation by microorganisms in the MBR contributed to 95.9% of the total removal. After the treatment, the concentration of antiandrogenic activity in the effluent was still 1.05 μg flutamide equivalence (FEQ)/L, 36.2% of which was due to strong polar extracts. In the anaerobic reactor, anoxic reactor, and membrane reactor system for coking wastewater treatment, the antiandrogenic activity of raw coking wastewater was 78.6 mg FEQ/L, and the effluent of the treatment system had only 0.34 mg FEQ/L. The antiandrogenic activity mainly existed in the medium strong polar and strong polar extracts. Biodegradation by microorganisms contributed to at least 89.2% of the total antiandrogenic activity removal in the system. Biodegradation was the main removal mechanism of antiandrogenic activity in both the wastewater treatment systems.     

Mercury adsorption characteristics of HBr-modified fly ash in an entrained-flow reactor

In this study, the mercury adsorption characteristics of HBr-modified fly ash in an entrained-flow reactor were investigated through thermal decomposition methods. The results show that the mercury adsorption performance of the HBr-modified fly ash was enhanced significantly. The mercury species adsorbed by unmodified fly ash were HgCl₂, HgS and HgO. The mercury adsorbed by HBr-modified fly ash, in the entrained-flow reactor, existed in two forms, HgBr₂ and HgO, and the HBr was the dominant factor promoting oxidation of elemental mercury in the entrained-flow reactor. In the current study, the concentration of HgBr₂ and HgO in ash from the fine ash vessel was 4.6 times greater than for ash from the coarse ash vessel. The fine ash had better mercury adsorption performance than coarse ash, which is most likely due to the higher specific surface area and longer residence time.     

Some properties of a sequencing batch reactor for treatment of wastewater containing thiocyanate compounds

Thiocyanate (SCN) compounds in photo-processing wastewater (PPWW) could be treated by an SBR system without any release of thiocyanate to the atmosphere during the aeration step. An SCN loading greater than 84 g m(-3)d(-1) showed negative effects on the growth of bio-sludge and removal efficiencies of the system. The acclimatization period of the system was increased with an increase in SCN concentration or loading. The COD, BOD(5), TKN, and SCN removal efficiencies were 96.0 +/- 1.6%, 72 +/- 2%, 49 +/- 5%, and 82 +/- 3%, respectively, under an SCN loading of up to 84 g m(-3)d(-1). The removal efficiency of the system was repressed by SCN due to the repressed growth rate of nitrification bacteria. However, the removal efficiency could be increased with an increase in HRT or a decrease in SCN loading. Also, increases in HRT or decreases in SCN loading led to increased sludge age or solid retention time (SRT) and decreased the sludge volume index (SVI) value. The SRT and SVI of the system with synthetic wastewater containing 840 mg l(-1) SCN under an HRT of 3 days (SCN loading of 280 g m(-3)d(-1)) were 3.9 +/- 0.7 days and 65 +/- 4 ml g(-1), respectively, while they were 11.2+/-0.8 days and 55 +/- 6 ml g(-1), respectively under an HRT of 10 days (SCN loading of 84 g m(-3)d(-1)).     

电活性生物膜阳极构建及其对2，4，6-三氯酚同步降解和产电

为实现氯酚（CPs）的高效降解和资源化利用,探究微生物燃料电池（MFC）体系优势功能菌,揭示生物降解路径.接种、驯化长春市南郊污水处理厂的厌氧活性污泥,获得生物膜阳极以构筑MFC-2,4,6-TCP体系,基于扫描电子电镜（SEM）、16S rRNA分析测序方法,考察生物膜阳极微生物的附着情况和优势菌种,基于电化学阻抗（EIS）、循环伏安（CV）和线性扫描伏安（LSV）等电化学分析手段,表征生物阳极的电化学性能和氧化还原能力.结果表明,生物膜阳极微生物种类丰富,其中Geobacter和Acinetobacter分别为MFC-2,4,6-TCP体系产电和降解驯化期的优势功能菌,体系最大输出电压可达0.55 V,最大功率密度为428.65 mW·m-2,对2,4,6-TCP的降解和矿化率可达97.5%和85.4%.随着MFC循环次数的增加,微生物代谢途径多样化,产电菌逐渐演替为协同菌,且优势功能菌对2,4,6-TCP降解的中间产物（环己醇）,其毒性远低于氯酚或苯酚,更利于被微生物利用.该结果可为氯酚废水的实际处理提供新策略和技术参考.