水环境中微囊藻毒素检测技术研究进展

随着世界各国对微囊藻毒素的重视,中国也在相关水质标准里新增了微囊藻毒素这项指标.因此,水环境中微囊藻毒素的检测和控制变得非常重要,而检测更是控制的基础.比较详细地综述了目前国内外在微囊藻毒素检测方面的各种不同的研究方法和成果;并在总结这些研究的基础上,展望了微囊藻毒素检测的发展方向.     

沸石滤料曝气生物滤池启动性能研究

沸石滤料曝气生物滤池 (ZBAF)对氨氮的去除包括生物硝化和离子交换两种作用。中试装置启动试验表明 ,初期对氨氮的去除以离子交换作用为主 ,末期以硝化作用为主 ,不能以氨氮总去除率达到稳定作为启动过程结束的标志 ,而应以氨氮硝化去除率达到稳定作为标志。沿程试验表明 ,硝化细菌对沸石的“生物再生功能” ,实质是已被沸石交换的氨氮被水中浓度较大的其他阳离子交换下来后 ,被硝化菌所利用的现象 ;沸石表面有生物膜时 ,仍具有交换氨氮能力     

浮动生物床/地下渗滤联合工艺处理校园污水的设计与管理

结合沈阳师范大学的校园污水处理实例,阐明地下渗滤与浮动生物床联合工艺的设计和运营管理的问题.实践证明,采用浮动生物床/地下渗滤工艺对生活污水进行深度处理,投资运行费用低、管理简单、出水水质稳定且优于所要求的回用水水质.     

低浓度硫化氢废气的液相催化氧化法净化实验研究

针对H2S浓度为750~1500mg/m3的气体的液相催化氧化技术进行了动力学实验研究。配制了以铁基离子作为主催化剂的复合吸收净化溶液,同时加入稳定剂和表面活性剂提高催化剂在碱性吸收溶液的活性。分别考察了原料气中H2S、O2含量以及吸收液中催化剂离子浓度、温度等因素对吸收速率的影响;确定了较为理想的吸收操作条件并获得了较好的吸收净化效果;饱和吸收液易于再生,净化性能恢复良好,可重复使用。     

多相催化-臭氧氧化法处理模拟有机磷农药废水

实验通过臭氧氧化法来降解模拟废水中的有机磷农药，将其转化为无害物质，并试验研究了在废水中加入2种自制的催化剂对降解结果的影响。采用气相色谱法测定水中有机磷农药的量。结果表明，只用臭氧处理的情况下1周后有机磷的去除率为78．03％；在催化剂A存在下，去除率可达93．85％；在催化剂B存在下，去除率可达为88．35％。结果表明，臭氧氧化法对此类污水：具有较好的降解作用，尤其在有催化剂存在的情况下处理效果更好，在室温和中性介质中均属于一级反应。     

提高LIFAC法脱硫效率的工程实例

针对LIFAC法脱硫效率低的问题，从吸收剂的涡流循环喷钙装置、增强吸收剂的活性、抑制脱硫产物硫酸钙的高温分解等几个方面进行了剖析，并自制LIFAC法廉价喷钙剂，在佛山华丰纸业有限公司进行中试，取得了脱硫率平均90％以上的效果，最后，作者对该技术的优越性进行了评估。     

Effect of alkalinity on the performance of a simulated landfill bioreactor digesting organic solid wastes

This study investigated the effects of alkalinity on the anaerobic treatment of the organic solid wastes collected from the kitchen of Engineering Faculty in Dokuz Eylul University, Izmir, Turkey and the leachate characteristics treated in three simulated landfill anaerobic bioreactors. All of the reactors were operated with leachate recirculation. One reactor was operated without alkalinity addition. The second reactor was operated by the addition of 3 g l-1 d-1 of NaHCO3 alkalinity to the leachate and the third reactor was operated by the addition of 6 g l-1 d-1 NaHCO3 alkalinity to the leachate. After 65 d of anaerobic incubation, it was observed that the chemical oxygen demand (COD), volatile fatty acids (VFA) concentrations, and biochemical oxygen demand to chemical oxygen demand (BOD5/COD) ratios in the leachate samples produced from the alkalinity added reactors were lower than the control reactor while the pH values were higher than the control reactor. The COD values were measured as 18900, 3800 and 2900 mg l-1 while the VFA concentrations were 6900, 1400 and 1290 mg l-1, respectively, in the leachate samples of the control, and reactors containing 3 g l-1 NaHCO3 and 6 g l-1 NaHCO3 after 65 d of anaerobic incubation. The total nitrogen (TN), total phosphorus (TP) and ammonium nitrogen (NH4-N) concentrations in organic solid waste (OSW) significantly reduced in the reactor containing 6 g l-1 NaHCO3 by d 65. The values of pH were 6.54, 7.19 and 7.31, after 65 d of anaerobic incubation, respectively, in the aforementioned reactors results in neutral environmental conditions in alkalinity added reactors. Methane percentage of the control, reactors containing 3 g l-1 NaHCO3 and 6 g l-1 NaHCO3 were 37%, 64% and 65%, respectively, after 65 d of incubation. BOD5/COD ratios of 0.27 and 0.25 were achieved in the 3 and 6 g l-1 NaHCO3 containing reactors, indicating a better OSW stabilization. Alkalinity addition reduced the waste quantity, the organic content of the solid waste and the biodegradation time.     

污泥酸化速率影响因子的探讨

采用城市污水厂污泥作为嗜酸微生物菌株来源,通过添加一定量的单质硫,使其中的嗜酸硫杆菌群大量增殖,并使污泥pH大幅降低.取得的培养物可用于废旧干电池中重金属沥滤等的处理.由于培养物对重金属沥滤效率和污泥的酸化速率密切相关,为此进行了不同的污泥种类、加硫量、污泥浓度和曝气强度对污泥酸化速率影响的实验.实验表明,初沉泥、二沉泥和混合浓缩污泥都能迅速利用硫产酸;加硫量(以100 mL污泥计)在0.5、1.0、2.0、4.0 g时,快速酸化的趋势相同.0.5 g的加硫量显示出略微慢的酸化速率,最后达到的最低pH在1.2左右,其他三个都降至1.0以下.污泥质量分数在0.5%、1.0%、2.0%、3.0%、4.0%时,也具有相同的酸化趋势,0.5%质量分数的污泥下降速率最快,这与较低浓度下污泥对pH的缓冲能力较小有关;曝气强度在0.45 L/min和0.3 L/min差别较小,5 d内能迅速降低pH,0.2 L/min的酸化速率较慢,足够长的时间(12 d)也能将pH降至2.5左右,0.1 L/min的曝气强度的酸化速率最慢,不能达到预期的酸化效果.     

浅谈电镀清洁生产技术与管理

介绍了电镀行业的清洁生产技术与加强清洁生产管理。通过发展环保技术，从源头削减和技术改造来减少污染物的产生量，不断加强企业清洁生产管理，促进电镀行业实现社会效益、经济效益和环境效益的统一，走可持续发展的道路。     

Aromatic photonitration in homogeneous and heterogeneous aqueous systems

This work describes the nitration of aromatics upon near-UV photolysis of nitrate and nitrite in aqueous solution and upon photocatalytic oxidation of nitrite in TiO2 suspensions. Phenol is used in this work as a model aromatic molecule and as a probe for *NO2/N2O4. The photoinduced nitration of phenol in aqueous systems occurs upon the reaction between phenol and *NO2 or N2O4, and is enhanced by the photocatalytic oxidation of nitrite to *NO2 by TiO2. Aromatic photonitration in the liquid phase can play a relevant role in the formation of nitroaromatics in natural waters and atmospheric hydrometeors, thus being a potential pathway for the condensed-phase nitration of aromatics. Furthermore, the photoinduced oxidation of nitrite to nitrogen dioxide suggests a completely new role for nitrite in natural waters and atmospheric aerosols.