5种植物材料的水解释碳性能及反硝化效率

碳源在硝酸盐去除过程中起电子供体的作用,是生物反硝化反应的关键物质之一。为解决污水处理脱氮时碳源不足抑制反硝化反应造成脱氮效率低的问题,本研究选取风车草、甘蔗渣、芦竹、美人蕉和稻草秆5种植物材料作为反硝化碳源,探讨不同植物材料的水解释碳能力和释放规律;并进一步以其水解液作为外加碳源,探讨其对反硝化脱氮效率的影响。研究结果表明,植物材料水解释碳过程符合二级动力学反应规律,不同植物材料的释碳能力具有显著性差异,以甘蔗渣在固液比1∶80时COD释放当量最大,为45.45 mg/L;添加植物水解液可显著提高反硝化脱氮效率,以芦竹水解液脱氮效果最好,达到71.9%。此外,碳氮比是影响脱氮效率的重要因素之一,以碳氮比为9时反硝化脱氮效果最佳。     

竹制填料生物接触氧化工艺处理污染河水简

针对受污染的湖溪河水质特征,以传统弹性塑料填料做对比,研究以竹球和竹丝为填料的生物接触氧化工艺,考察填料的挂膜时间、生物量和污水处理效果;确定连续曝气和间歇曝气时反应器的最优运行工况：连续曝气时为HRT=7.5 h,DO=3 mg/L;间歇曝气时为厌氧1.2 h、好氧6.3 h交替运行。实验结果表明,与弹性塑料填料相比,竹制填料挂膜速度快,竹球填料的水处理效果最好;连续曝气最优工况下竹球填料反应器中COD、TN、NH₃-N和TP的平均去除率分别为66.7%、47.9%、57.1%和30.6%;间歇曝气最优工况下竹球填料反应器中COD、TN、NH₃-N和TP的平均去除率分别64.08%、39.95%、60.7%和54.68%;竹制填料可替代传统的塑料填料作为生物接触氧化工艺的载体填料。     

电催化氧化处理除草剂异噁草酮废水的效能

为有效处理含异噁草酮除草剂废水,以Sb掺杂Ti／SnO2电极为阳极,不锈钢板为阴极,采用电催化氧化技术对异噁草酮废水进行降解,研究了不同影响因素对异噁草酮去除率的影响,并分析了异噁草酮的降解效果。结果表明,当异噁草酮初始浓度为100mg／L、电流密度为20mA／cm2、电解质投加量为0．10mol／L,反应120min后,异噁草酮去除率达到94％,此时TOC去除率为57．9％,能耗为25kWh／m2,且废水的可生化性能显著提高。     

南京某城市污水二级处理系统中酞酸酯类的分布及去除特征

以南京某城市污水厂污水和污泥中的酞酸酯类（PAEs）为研究对象,分别采用固相萃取-气相色谱-质谱联用（SPE—Gc．Ms）和超声提取．气相色谱．质谱联用（USE—GC—Ms）检测其中的优先控制污染物邻苯二甲酸二甲酯（DMP）、邻苯二甲酸二乙酯（DEP）、邻苯二甲酸二丁酯（DBP）和邻苯二甲酸单（2-乙基己基）酯（MEHP）,研究其在厌氧／好氧（A／O）污泥处理过程中的分布特征及降解规律。研究结果表明,各类PAEs在该污水厂的污水和污泥中均有检出,二级处理出水中4种酞酸酯类物质的浓度在0．151—2．419μg／L。污水中4种酞酸酯的分布规律为MEHP〉DBP〉DMP〉DEP,污泥中4种酞酸酯的分布规律为MEHP〉DBP〉DEP〉DMP。该污水厂二级处理工艺对4种PAEs的去除效果较明显,去除效率DBP〉DEP〉DMP〉MEHP．     

发酵类抗生素废水处理工艺及运行效果

介绍了内蒙古某抗生素废水处理厂的处理工艺流程、处理单元类型及其详细设计参数,通过对该污水处理厂半年内运行效果的调研,分析评价该污水处理系统的处理效果及出水指标;该水厂工艺流程对COD、TOC、氨氮、总氮、总磷、BOD和急性毒性的平均去除率分别为96.52%、95.83%、50.24%、55.20%、62.05%、98.52%和99.14%,COD、氨氮、总氮、总磷出水水质分别为477、438、556.7和7.69 mg/L,达到排放到城区下水道要求,园区内所有废水汇集到园区污水处理厂进行集中深度处理达标后排放水体。通过对该水厂工艺的介绍和水质分析,为我国抗生素生产企业面临的废水处理工艺类型选择及工程改造升级提供一定参考。     

宝钢焦化废水处理脱氮研究与实践

针对上海提高新排放标准中总氮(TN)≤35 mg/L的要求,对焦化废水进行了脱氮研究。选取现场缺氧-好氧-好氧(A-O-O)工艺中前两段的A-O生化沉淀池1出水,在SBR内进行反硝化脱氮实验,考察葡萄糖、葡萄糖+乙酸钠、甲醇和甲醇+乙酸钠单一或复合碳源及投加反硝化菌种对脱氮的影响,确定最佳碳源为甲醇+乙酸钠,最佳反硝化水力停留时间为16 h。当反硝化菌液投加浓度为1 mg/L时,SBR出水TN满足达标排放要求。结合实验结果对宝钢焦化废水原有AO-O工艺改造升级为A-O-A-O二段脱氮工艺,并对生化出水实施进一步的物化混凝处理。改造后,工艺长期运行稳定,最终出水完全达到上海市污水综合排放标准(DB 31/199-2009)TN≤35 mg/L的要求,并满足氰化物、氟化物以及COD的排放要求。     

Industrial wastewater pre-treatment for heavy metal reduction by employing a sorbent-assisted ultrafiltration system

This work examined the adoption of a sorbent-assisted ultrafiltration (UF) system for the reduction of Pb(II), Cu(II), Zn(II) and Ni(II) from industrial wastewater. In such a system metals were removed via several processes which included precipitation through the formation of hydroxides, formation of precipitates/complexes among the metal ions and the wastewater compounds, adsorption of metals onto minerals (bentonite, zeolite, vermiculite) and retention of insoluble metal species by the UF membranes. At pH = 6 the metal removal sequence obtained by the UF system was Pb(II) > Cu(II) > Zn(II) > Ni(II) in mg g⁻¹ with significant amount of lead and copper being removed due to chemical precipitation and formation of precipitates/complexes with wastewater compounds. At this pH, zinc and nickel adsorption onto minerals was significant, particularly when bentonite and vermiculite were employed as adsorbents. Metal adsorption onto zeolite and bentonite followed the sequence Zn(II) > Ni(II) > Cu(II) > Pb(II), while for vermiculite the sequence was Ni(II) > Zn(II) > Cu(II) > Pb(II) in mg g⁻¹. The low amount of Pb(II) and Cu(II) adsorbed by minerals was attributed to the low available lead and copper concentration. At pH = 9 the adoption of UF could effectively reduce heavy metals to very low levels. The same was observed at pH = 8, provided that minerals were added. The prevailing metal removal process was the formation of precipitates/complexes with wastewater compounds.     

Zero-valent iron nanoparticles in treatment of acid mine water from in situ uranium leaching

Acid mine water from in situ chemical leaching of uranium (Straz pod Ralskem, Czech Republic) was treated in laboratory scale experiments by zero-valent iron nanoparticles (nZVI). For the first time, nZVI were applied for the treatment of the real acid water system containing the miscellaneous mixture of pollutants, where the various removal mechanisms occur simultaneously. Toxicity of the treated saline acid water is caused by major contaminants represented by aluminum and sulphates in a high concentration, as well as by microcontaminants like As, Be, Cd, Cr, Cu, Ni, U, V, and Zn. Laboratory batch experiments proved a significant decrease in concentrations of all the monitored pollutants due to an increase in pH and a decrease in oxidation-reduction potential related to an application of nZVI. The assumed mechanisms of contaminants removal include precipitation of cations in a lower oxidation state, precipitation caused by a simple pH increase and co-precipitation with the formed iron oxyhydroxides. The possibility to control the reaction kinetics through the nature of the surface stabilizing shell (polymer vs. FeO nanolayer) is discussed as an important practical aspect.     

XAFS study of starch-stabilized magnetite nanoparticles and surface speciation of arsenate

It has been shown that starch can effectively stabilize nanoscale magnetite particles, and starch-stabilized magnetite nanoparticles (SMNP) are promising for in situ remediation of arsenic-contaminated soils. However, a molecular level understanding has been lacking. Here, we carried out XAFS studies to bridge this knowledge gap. Fe K-edge XAFS spectra indicated that the Fe-O and Fe-Fe coordination numbers of SMNP were lower than those for bare magnetite particles, and these coordination numbers decreased with increasing starch concentration. The decrease in the average coordination number at elevated stabilizer concentration was attributed to the increase in the surface-to-volume ratio. Arsenic K-edge XAFS spectra indicated that adsorbed arsenate on SMNP consisted primarily of binuclear bidentate (BB) complexes and monodentate mononuclear (MM) complexes. More BB complexes (energetically more favorable) were observed at higher starch concentrations, indicating that SMNP not only offered greater adsorption surface area, but also stronger adsorption affinity toward arsenate.     

粗MnSO4溶液中MnS2O6的去除条件研究

用软锰矿吸收SO2生成MnSO4时会伴随有副产物MnS2O6生成。产品中MnS2O6的存在会降低硫酸锰产品质量,同时会缓慢释放出SO2气体污染环境。本文用单因素实验方法研究了粗MnSO4溶液中MnS2O6的最优去除条件。研究结果显示,软锰矿用量为12.2 g,硫酸加入量为20 mL、反应温度100℃、反应时间3 h、搅拌速度500 r/min,MnS2O6的去除率可达91%以上。其最终产品能达到GB1622-1986一级品标准。