阴极材料对三相三维电极反应器电解处理酸性橙7的影响研究

采用具有不同阴极材料的三相三维电极反应器,对300 mg/L酸性橙7(AO7)模拟废水进行处理研究,重点考察阴极材料对脱色率和反应体系矿化能力的影响,同时利用HPLC、UV-Vis、GC-MS等分析方法对·OH、H2O2以及降解产物进行测定,探讨了3种电极对AO7的降解行为.结果表明,在电压20 V条件下电解60 min后,活性炭纤维(ACF)、石墨和不锈钢等3种阴极体系对于AO7的脱色率均高于96%,三者之间没有明显差别.但是ACF体系对TOC的去除率可达到57.4%,高于其它两者.3种阴极体系中均有高活性的·OH和H2O2生成,但是ACF阴极体系中产生的浓度较高,从而决定了其具有较高的矿化能力.几种不同电极体系电解AO7过程中都遵循了相同的产生酮类和萘酚类物质的过程.     

台州市酸雨污染现状及其对策分析

通过对近十年来的酸雨监测资料的收集分析,结合同期台州市大气环境中二氧化硫和氮氧化物的监测数据,采用秩相关系数法,对酸雨污染趋势和成因进行分析和讨论,并提出针对性措施,以期为台州市以及类似地区的大气污染、酸雨污染等防治工作提供政策参考。     

H-酸的催化湿式氧化反应过程研究

湿式氧化（ＷＡＯ）和催化湿式氧化（ＣＷＡＯ）都能有效地处理染料中间体－－Ｈ－酸。所有的Ｈ－酸在５ｍｉｎ内均被支除和形成一些中间产物。在不同反应时间段测定了ｐＨ值及阴、阳离子和小分子有机酸等中间产物。分析表明,ｐＨ值与ＣＯＤ的去除及有机酸的产生有密切的联系,Ｈ－酸被氧化成ＮＨ４＾＋、ＳＯ４＾２－、ＨＣＯＯＨ和ＣＨ２ＣＯＯＨ。ＷＡＯ法的瓜速率慢而且氧化乙酸困难。而ＣＷＡＯ法的反应速率不但快而且能有效地     

不同环境条件下偶氮染料酸性大红GR的生物降解性能

为了考察不同环境条件下偶氮染料酸性大红GR生物降解性能,采用已驯化的混合菌群作为接种液进行偶氮染料酸性大红GR脱色试验。结果表明,微氧条件下(静置敞口培养),偶氮染料酸性大红GR脱色效果最佳,染料脱色主要发生在菌体的对数生长期。混合菌群对pH、温度适应范围较广,pH为3.32~9.18,温度在20℃~37℃范围内均可以获得较好脱色效果,脱色率均在80%以上。微氧条件下酸性大红GR降解历程表明,偶氮基整个共轭系统被破坏,生成了一种新的结构,使原有的某些精细结构在二阶导数光谱中得以表现,由此探讨其生物降解机理。     

Fenton试剂处理酸性玫瑰红B的研究

采用Fenton试剂处理酸性玫瑰红B染料废水,考察了FeSO4投加量、H2O2投加量、pH值和反应时间对处理效果的影响,研究了原水的氧化还原电位和TOC的变化规律,评价了它的可生化性。结果表明,最佳pH值为3,FeSO4的适宜投加量为8mmol/L,H2O2最佳投加量为50mmol/L,此时COD去除率和脱色率分别为77.1%和92.8%,处理后该染料废水的可生化性大大提高。     

强磁场影响下菌株B1对染料的脱色作用

从校园土壤中筛选出一株对人工合成染料酸性红B有一定脱色能力的菌株B1(芽孢杆菌属),经过6.0、8.0、8.0T的强磁场分别作用30、15、30 min后进行了脱色试验;根据实验数据,得到染料脱色模型.结果表明,强磁场对B1具有诱变作用,能使其脱色能力得到强化.     

分子识别作用下光催化降解偶氮染料酸性红GR

合成了β-环糊精(β-CD)与偶氮染料酸性红GR(ARGR)的包结物,并采用红外光谱仪对ARGR、β-CD及β-CD与ARGR的包结物进行了表征,表征结果显示,β-CD与ARGR的包结物的特征峰的峰形和强度与β-CD相似,但峰位有明显的偏移,说明ARGR进入了β-CD空腔与β-CD发生了分子识别作用。采用TiO2作为催化剂,研究了β-CD分子识别后ARGR的光催化降解行为,实验结果表明,在ARGR质量浓度为20.0 mg/L、β-CD浓度为1.8×10-5 mol/L、体系pH为4.0、TiO2加入量为1.0 g/L、光催化反应时间为60 min的条件下,经β-CD分子识别后ARGR的光催化降解率可达100%。     

Tissue S/N ratios and stable isotopes (δS and δN) of epilithic mosses (Haplocladium microphyllum) for showing air pollution in urban cities in Southern China

In urban cities in Southern China, the tissue S/N ratios of epilithic mosses (Haplocladium microphyllum), varied widely from 0.11 to 0.19, are strongly related to some atmospheric chemical parameters (e.g. rainwater SO₄²⁻/NH₄⁺ ratios, each people SO₂ emission). If tissue S/N ratios in the healthy moss species tend to maintain a constant ratio of 0.15 in unpolluted area, our study cities can be divided into two classes: class I (S/N > 0.15, S excess) and class II (S/N < 0.15, N excess), possibly indicative of stronger industrial activity and higher density of population, respectively. Mosses in all these cities obtained S and N from rainwater at a similar ratio. Sulphur and N isotope ratios in mosses are found significantly linearly correlated with local coal δ³⁴S and NH₄⁺-N wet deposition, respectively, indicating that local coal and animal NH₃ are the major atmospheric S and N sources.     

Review on the use of enzymes for the detection of organochlorine, organophosphate and carbamate pesticides in the environment

Pesticides are released intentionally into the environment and, through various processes, contaminate the environment. Three of the main classes of pesticides that pose a serious problem are organochlorines, organophosphates and carbamates. While pesticides are associated with many health effects, there is a lack of monitoring data on these contaminants. Traditional chromatographic methods are effective for the analysis of pesticides in the environment, but have limitations and prevent adequate monitoring. Enzymatic methods have been promoted for many years as an alternative method of detection of these pesticides. The main enzymes that have been utilised in this regard have been acetylcholinesterase, butyrylcholinesterase, alkaline phosphatase, organophosphorus hydrolase and tyrosinase. The enzymatic methods are based on the activation or inhibition of the enzyme by a pesticide which is proportional to the concentration of the pesticide. Research on enzymatic methods of detection, as well as some of the problems and challenges associated with these methods, is extensively discussed in this review. These methods can serve as a tool for screening large samples which can be followed up with the more traditional chromatographic methods of analysis.     

Speciation and transport of arsenic in an acid sulfate soil-dominated catchment, eastern Australia

Factors controlling the transport of geogenically-derived arsenic from a coastal acid sulfate soil into downstream sediments are identified in this study with both solid-phase associations and aqueous speciation clearly critical to the mobility and toxicity of arsenic. The data from both sequential extractions and X-ray adsorption spectroscopy indicate that arsenic in the unoxidised Holocene acid sulfate soils is essentially non-labile in the absence of prolonged oxidation, existing primarily as arsenopyrite or as an arsenopyrite-like species, likely arsenian pyrite. Anthropogenically-accelerated pedogenic processes, which have oxidised this material over time, have greatly enhanced the potential bioavailability of arsenic, with solid-phase arsenic almost solely present as As(V) associated with secondary Fe(III) minerals present. Analyses of downstream sediments reveal that a portion of the arsenic is retained as a mixed As(III)/As(V) solid-phase, though not at levels considered to be environmentally deleterious. Determination of arsenic speciation in pore waters using high performance liquid chromatography/Inductively Coupled Plasma-Mass Spectrometry shows a dominance of As(III) in upstream pore waters whilst an unidentified As species reaches comparative levels within the downstream, estuarine locations. Pore water As(V) was detected at trace concentrations only. The results demonstrate the importance of landscape processes to arsenic transport and availability within acid sulfate soil environments.