Atrazine removal by ozonation processes in surface waters

Abstract

Atrazine (6‐chloro‐N‐ethyl‐N'‐isopropyl‐1,3,5‐triazinedyl‐2,4‐diamine) was treated with ozone alone and in combination with hydrogen peroxide or UV radiation in three surface waters. Experiments were carried out in two bubble reactors operated continously. Variables investigated were the ozone partial pressure, temperature, pH, mass flow ratio of oxidants fed: hydrogen peroxide and ozone and the type of oxidation including UV radiation alone. Residence time for the aqueous phase was kept at 10 min. Concentrations of some intermediates, including deethylatrazine, deisopropylatrazine and deethyldeisopropylatrazine, were also followed. The nature of water, specifically the alkalinity and pH were found to be important variables that affected atrazine (ATZ) removal. Surface waters with low alkalinity and high pH allowed the highest removal of ATZ to be reached. There was an optimum hydrogen peroxide to ozone mass flow ratio that resulted in the highest ATZ removal in each surface water treated. This optimum was above the theoretical stoichiometry of the process. Therefore, to reach the maximum removal of ATZ in a O₃/H₂O₂ process, more hydrogen peroxide was needed in the surface waters treated than in ultrapure water under similar experimental conditions. In some cases, UV radiation alone resulted in the removal of ATZ higher than ozonation alone. This was likely due to the alkalinity of the surface water. Ozonation and UV radiation processes yield different amounts of hydrogen peroxide. Combined ozonations (O₃/H₂O₂ and O₃/UV) lead to ATZ removals higher than single ozonation or UV radiation but the formation of intermediates was higher.     

气田井喷硫化氢风洞模拟试验研究

为研究高含硫气田发生井喷事故后硫化氢的扩散运动规律,以重庆开县"12·23"井喷事故为研究对象,利用北京大学的2号环境风洞,制作了1∶2000的比例模型,利用乙烯和丙烯的混合气为示踪气体,采用长采样管方法测量浓度,首次在国内进行了井喷事故后硫化氢扩散的风洞试验,获得了低风速下(源处10m高风速为0.5m/s)N,NE,E,SE,S,SW,W,NW8个风向情况下的硫化氢浓度分布随时间的演化动画,定量地给出了各风向情况下硫化氢的最大浓度分布和各点的浓度时间序列,认为在低风速下,最大硫化氢浓度区域在撞山爬坡时出现,而爬过山坡后在背风区的硫化氢浓度会迅速降低。研究成果将为气田的井喷风险分级以及井喷事故后的应急处理提供参考。     

A sulfur removal and disposal process through H2S adsorption and regeneration: Ammonia leaching regeneration

An iron oxide solid sponge H₂S adsorbent works by reacting H₂S and turning ferric oxide into ferric sulfide. The ferric sulfide will be converted back into ferric oxide and elemental sulfur when contacting oxygen or air. This study investigates the leaching of elemental sulfur from the solid sponge using anhydrous liquid ammonia as solvent. The leaching treatment expectedly results in effective regeneration of the adsorbent, which is able to lead to a sulfur removal and recovery process suitable for handling the small and mid-sized sulfur production cases, i.e., those less than 10 ton/day sulfur. The leaching does not significantly impair the physical properties, including the adsorbent pellet strength. The adsorption–regeneration (or leaching) cycle could be repeated at least three times. The cumulative sulfur loading can achieve as high as 50% (w/w), three times greater than that in the one-time use. The wash-off in leaching and the spent adsorbent can be made into slurry that is to be injected into underground formations such as depleted oil wells. It is anticipated that this underground injection is safer and more efficient than acid gas injection.     

火电厂燃煤烟气过氧化氢脱硝技术的研究及应用

H2O2脱硝工艺是面向火电厂烟气污染物控制的一种环境友好型控制技术。通过对H2O2脱硝反应机理、关键影响因素、工艺路线和经济性等方面研究,综述了国内外H2O2脱硝技术研究进展,分析了不同工艺中存在的问题,并针对存在的问题进行了探讨。     

Ce-Mn双金属氧化物深度催化氧化废气中的氯甲苯

采用Ce-Mn双金属氧化物深度催化氧化废气中的氯甲苯。实验结果表明:当n(Ce):n(Mn)为1:5时,CeO_2与MnO_x之间的协同效应最大,对氯甲苯的去除效果最好;在以纯氧为氧化剂、反应温度为360℃、氯甲苯体积分数为0.5%～1.5%、体积空速为12 000～30 000 h~(-1)的条件下,氯甲苯去除率可达100%。     

城市污水处理厂除臭生物滤池运行效果及影响因素研究

对山东某城市污水处理厂散发的恶臭气体进行除臭研究,考察了除臭生物滤池的运行效果、工艺影响因素和除臭生物滤池内微生物相特点。结果表明:(1)在进气量为828 m3/h、气体停留时间为30 s、硫化氢和氨进气质量浓度分别为0.5~28.4、0.9~34.3 mg/m3的条件下,稳定运行时,大部分时间硫化氢和氨去除率分别达98%和80%以上,而且除臭生物滤池对于进气负荷具有较强的抗冲击能力。(2)当填料含湿量为43.6%~63.4%时,硫化氢去除率在90%以上;氨去除受填料含湿量的影响较大,填料含湿量越高越利于氨的去除。(3)在处理低浓度含硫化氢和氨的恶臭气体时,生物除臭工程可以在低填料pH(3.0左右)下长期运行,并保持较高的恶臭气体去除率。(4)运行第60天后,当温度为10℃以上时,硫化氢和氨去除率几乎不受影响;第169天后,当温度降至10℃以下时,硫化氢和氨去除率均有一定程度的下降,最低分别为94.6%和79.8%。(5)除臭生物滤池稳定运行时,优势硫氧化菌主要为嗜酸性硫细菌。     

An economic evaluation on the purification and storage of waste hydrogen for the use of fuel cell scooters

Safe and reliable metal hydride canisters (MHCs) for the use of hydrogen storage at low pressure can be applied to supply small fuel cell vehicles or scooters with hydrogen fuel. However, greater cost-effectiveness of hydrogen gas is obviously necessary to the successful promotion of hydrogen fuel cell scooters in the market. In this study, we use the net present value (NPV) method to evaluate the feasibility of an investment project on the supply of purified hydrogen in a pulp company at Hualien, Taiwan. The purified hydrogen can be separated from waste hydrogen by using pressure swing adsorption (PSA) technology and then be stored in MHCs. Under some assumptions of improved parameters about hydrogen production cost and hydrogen gas price, the discounted payback period of hydrogen purification and storage project in our study can be less than 10 years and the unit cost of hydrogen gas can be close to the price of gasoline. Moreover, the unit cost of hydrogen gas in our study can be lower than the cost from other sources of hydrogen.     

磷酸盐对硫化亚铁(FeS)吸附Sb(Ⅲ)的影响机理研究

还原环境(如湖泊、海洋沉积物)中,FeS是重金属的重要载体。在富营养化过程中,磷酸盐可能对重金属在FeS上的吸附行为产生重要影响。本文通过不同pH、磷酸盐浓度的批次试验,结合X射线衍射仪(XRD)和场发射透射电子电镜-能谱仪(TEM-EDS)固体分析手段,进行磷酸盐对FeS吸附Sb(Ⅲ)的影响研究。结果表明：酸性和中性条件下,磷酸盐会与FeS溶解释放的Fe(Ⅱ)反应生成磷酸亚铁沉淀,促进FeS溶解,同时释放出更多的H₂S(aq)/HS^-与Sb(Ⅲ)结合形成Sb₂S₃沉淀,从而促进溶液中Sb(Ⅲ)的吸附。碱性条件下,FeS对Sb(Ⅲ)只有吸附作用,而磷酸盐会占据FeS表面部分的吸附位点,与Sb(Ⅲ)形成竞争关系,进而抑制溶液中Sb(Ⅲ)的吸附。     

车载储氢瓶泄漏及车库内通风方式研究

为研究车库内燃料电池汽车氢气意外泄漏后的浓度分布情况,采用ANSYS软件,通过分析可燃性气体体积、水平方向和垂直方向氢气的扩散分布、不同泄漏位置氢气的扩散情况,研究6种不同通风方式对氢气意外泄漏扩散分布的影响,针对车库内氢气泄漏的特性,在通风方式上引入侧墙底部送风和侧墙顶部送风方式。研究结果表明：底部送风能显著加快氢气的扩散和排出。垂直高度上氢气浓度分布不均,侧墙顶部送风能使顶部堆积的氢气向下扩散,降低最大气体浓度;在墙角泄漏会由于墙壁的影响导致氢气堆积,对墙角局部通风尤为重要。研究结果可为氢燃料电池汽车专用车库的通风设计提供重要参考。     

对氯苯甲酸用于测量OH#方法探讨1.机理研究

对氯苯甲酸被用于臭氧氧化过程中羟基自由基的测量,为了检验对氯苯甲酸是否在测量过程中出现误差,进行了臭氧氧化对氯苯甲酸的间歇实验和半连续实验.结果表明,中性条件下间歇试验中,对氯苯甲酸可以强烈促进臭氧分解,它促进臭氧分解的能力比典型的促进剂甲酸和甲醇高10倍.半连续试验的结果进一步表明,臭氧氧化对氯苯甲酸时,可以形成中间产物过氧化氢,过氧化氢能和臭氧反应,形成大量的OH.,从而改变O3/OH.的链式反应,导致采用对氯苯甲酸测量OH.时出现误差.