Enhanced cyanogen chloride formation after UV/PS and UV/H2O2 pre-oxidation and chlorination in natural river water

Ultraviolet/persulfate (UV/PS) and Ultraviolet/hydrogen peroxide (UV/H₂O₂) have attracted much attention in recent years as advanced oxidation processes for water treatment. However, it is not all clear how these two methods affect the formation of cyanogen chloride (CNCl) in the subsequent water chlorination process. In this study, it was found that both UV/H₂O₂ and UV/PS pre-oxidation promoted the formation of CNCl in six actual water samples collected from urban rivers. Glycine, uric acid, arginine and histidine were investigated as the model compounds to explore the effects of different methods on the production of CNCl. The results showed that compared with chlorination alone, pre-oxidation by UV/H₂O₂ and UV/PS can reduce the production of CNCl for glycine and uric acid by up to 95% during post-chlorination process. However, they can greatly promote the formation of CNCl for arginine and histidine by up to 120-fold. In a more detailed investigation, pre-oxidation of histidine formed highly reactive intermediates to chlorine, leading to increased CNCl formation and chlorine consumption. The results showed that the precursors of CNCl was altered after pre-oxidation, and need to be re-evaluated.     

水稻烤田期间N2O排放及其影响因素

水稻田间实验研究了烤田期间的土壤温度、Eh、含水量和裂缝基本性质,矿质态氮以及与氮有关的酶活性的演变规律,及其对N2O排放的影响.试验表明,在水稻分蘖期间烤田,N2O有一个排放高峰,其最高值可达75.6μg·m-2·h-1.在排放高峰后,即使继续烤田,N2O的排放值也将降低.N2O排放与尿素氮肥的施用量没有明显关系.裂缝的生成,改变了N2O的日排放规律.随着烤田时间的延长,脲酶和羟胺还原酶活性呈波动变化,硝酸还原酶活性递减,亚硝酸还原酶活性极低.硝酸还原酶活性与N2O排放之间没有显著相关性.土壤中的脲酶活性与N2O日排放通量呈显著的线性正相关.在烤田期间,NO-3含量呈增加趋势.土壤中的硝态氮含量与N2O排放通量之间呈显著正线性关系.土壤中的铵态氮含量与N2O排放通量之间呈显著负线性相关.     

Geological CO2 Storage as a Climate Change Mitigation Option

Carbon dioxide (CO₂₎ capture and storage is increasingly being considered as an important climate change mitigation option. This paper explores provisions for including geological CO₂ storage in climate policy. The storage capacity of Norway's Continental Shelf is alone sufficient to store a large share of European CO₂ emissions for many decades. If CO₂ is injected into oil reservoirs there is an additional benefit in terms of enhanced oil recovery. However, there are significant technical and economic challenges, including the large investment in infrastructure required, with related economies of scale properties. Thus CO₂ capture, transportation and storage projects are likely to be more economically attractive if developed on a large scale, which could mean involving two or more nations. An additional challenge is the risk of future leakages from storage sites, where the government must take on a major responsibility. In institutional and policy terms, important challenges are the unsettled status of geological CO₂ storage as a policy measure in the Kyoto Protocol, lack of relevant reporting and verification procedures, and lack of decisions on how the option should be linked to the flexibility mechanisms under the Kyoto Protocol. In terms of competitiveness with expected prices for CO₂ permits under Kyoto Protocol trading, the relatively high costs per tonne of CO₂ stored means that geological CO₂ storage is primarily of interest where enhanced oil recovery is possible. These shortcomings and uncertainties mean that companies and governments today only have weak incentives to venture into geological CO₂ storage.     

纳米TiO2光催化反应器研究进展

光催化氧化作为一种高级氧化技术,在环境工程治理领域得到较快的发展。主要介绍了纳米TiO2光催化反应器近年来的研究进展,对各类型反应器的优缺点进行了深入分析,并展望了催化反应器应用前景。     

纳米金红石TiO2的转晶及声催化降解偶氮品红的研究

利用超声波结合过氧化氢(H2O2)使纳米金红石型TiO2转晶,制备出了大约含有30%锐钛相的转晶纳米TiO2.通过TiO2催化超声降解偶氮品红的研究证实了转晶纳米TiO2粉末具有明显的声催化活性.除此之外,还考察了各种因素对转晶纳米TiO2催化超声降解偶氮品红反应的影响.结果表明,在转晶纳米TiO2催化剂的作用下,偶氮品红的超声降解效果明显优于使用纳米金红石型和纳米锐钛型TiO2的情况.偶氮品红的声催化降解过程符合一级动力学反应.在超声波频率40 kHz、输出功率50 W、催化剂用量1000 mg·L-1、pH为5.00、温度为20℃、偶氮品红水溶液初始浓度20 mg·L-1的条件下,照射40 min时的降解率即可达到75%以上.     

Ni2+对2-氯酚厌氧降解系统的影响

针对重金属对难降解有毒有机物厌氧降解的影响问题,采用间歇试验法研究Ni2 对2-氯酚(2-CP)厌氧降解系统的影响规律.结果表明,当ρ(Ni2 )＜5 mg/L时,Ni2 对2-CP厌氧降解表现出轻度促进,当ρ(Ni2 )为5～500 mg/L,Ni2 以抑制作用为主,抑制作用随ρ(Ni2 )的增加而增强.Ni2 对原基质及关键中间产物苯酚和苯甲酸的抑制程度表现为:苯酚＞苯甲酸＞2-CP;ρ(Ni2 )低时的驯化能有效提高厌氧污泥对Ni2 毒性的耐受性能,300 mg/L Ni2 对2-CP降解的抑制从驯化前的65%降至驯化后的21%.Ni2 对2-CP厌氧降解的抑制作用与污泥中Ni的截留量之间存在正相关关系.抑制浓度CIP值和方程αC=[1-(I/I*)m]/[1 (I/I*)n)]能较好地表征厌氧生物处理过程受抑制程度.     

胞外聚合物、Ca2+及pH值对生物絮凝作用的影响

应用阳离子交换树脂从活性污泥中提取了胞外聚合物(EPS),考察了EPS、Ca2 及pH值对生物絮凝作用的影响.结果表明,当pH≥7.5, EPS≥70mg/L,[Ca2 ]≥300mg/L时,有利于生物絮体的形成.通过正交试验,得出pH值、EPS和[Ca2 ]对生物絮体形成综合影响的回归方程: h浊度= -901.70 97.35pH 1.96[Ca2 ] 9.08EPS-0.11pH[Ca2 ]-0.91pHEPS-0.02[Ca2 ]EPS 0.0021pH[Ca2 ]EPS.回归分析表明,pH值对生物絮体形成影响最显著,其次是EPS和Ca2 .     

微生物脱臭研究应用进展

随着恶臭气体污染成为环境污染的重大问题,对恶臭气体的控制和治理逐渐兴起。文章论述了用微生物法治理恶臭气体污染的基本原理,国内外研究现状以及主要工艺的类型和特点。讨论微生物法的主要影响因素,总结其存在的问题,并对发展趋势做了介绍。     

铁屑/焦炭/H_2O_2法预处理焦化废水的试验研究

采用铁屑/焦炭/H2O2法对焦化废水进行处理,通过单因素试验法考察了铁炭比、铁炭用量、H2O2用量、废水pH以及反应时间对处理效果的影响,并确定了最适工艺条件。结果表明,铁屑/焦炭/H2O2法与常规的铁屑内电解法相比,可显著提高焦化废水的预处理效果,并缩短反应时间。铁屑/焦炭/H2O2法处理焦化废水的最适条件为:铁炭比为4,铁炭用量为300mg/L铁屑+75mg/L焦炭,H2O2用量为1000mg/L,pH为3,反应时间20min。在此条件下,COD、色度、NH3-N和CN-的去除效率分别可达61.2%、74.0%、56.2%和74.3%,B/C比由处理前的0.189提高到0.387,处理水可生化性良好。铁屑/焦炭/H2O2可作为焦化废水的一种有效的预处理方法。     

金鱼藻对Cu2+的生物吸附特征

研究了沉水植物金鱼藻对Cu2 的吸附动力学及热力学特征.结果表明,金鱼藻对Cu2 的吸附在20min内达到平衡,吸附动力学的实验结果符合伪二级动力学方程,其相关系数达到0.9937,表明该吸附为多种反应同时作用的复杂过程.用Langmuir和Freundlich2种吸附等温式拟合吸附热力学的实验结果表明,以Langmuir模型拟合效果更好,相关系数为0.9977,其最大吸附量为7.79mg/g.在解吸实验中,各浓度组的解吸率均在1%以下,表明金鱼藻对Cu2 的吸持作用较强.