臭氧与氯联合消毒对钱塘江水源水DBPs形成及溴取代的影响

本文研究了在pH 6～8、反应时间2～72 h、反应温度10～30℃条件下,钱塘江水源水在臭氧-氯消毒联合作用下,三卤甲烷(THMs)、二卤乙酸(DHAAs)、三卤乙酸(THAAs)、二卤乙腈(HANs)、三卤硝基甲烷(THNMs)等5类消毒副产物(DBPs)的形成和溴取代特征.结果显示,臭氧-氯消毒下DBPs的形成与氯消毒有较多相似之处:①大部分DBPs形成量均随着温度的升高、时间的延长而增加,相应的溴取代因子(BSFs)则随着时间的延长、温度的上升而呈下降趋势;②氯代DHANs倾向于在酸性条件下形成多,而溴代DHANs则倾向于在碱性条件下形成多;③不管是氯消毒还是臭氧-氯消毒,也不管是哪种消毒条件,5类DBPs的BSF值顺序均为BSF_(HNMs)BSF_(DHANs) BSF_(THAAs)BSF_(THMs)≈BSF_(DHAAs).但与氯消毒不同的是,臭氧-氯消毒下THMs、DHAAs、THAAs、HANs的形成产量更低,而THNMs的产量则更高;而且与氯消毒相比,臭氧-氯消毒普遍增加了DBPs的溴取代程度,也改变了溴离子在不同DBPs之间的分配,即减少了THMs、DHAAs、THAAs、DHANs对溴的利用率,但大幅增加了HNMs的溴利用率.鉴于溴代HNMs的极高毒性,因此对于钱塘江水源水,臭氧-氯消毒要注意HNMs带来的健康风险.     

太湖、钱塘江取水口底泥及周边土壤有机物形成消毒副产物的特征研究

底泥、土壤均是水体有机物的重要来源,但目前相关消毒副产物(DBPs)形成方面的研究偏少.本研究以长三角重要水源地太湖、钱塘江取水口的底泥和周边土壤的浸出液为研究对象,探索氯、臭氧+氯、氯胺、臭氧+氯胺4种消毒方式下,三卤甲烷(THMs)、卤代酮(HKs)、卤乙腈(HANs)、卤代硝基甲烷(HNMs)的形成情况.结果表明,太湖、钱塘江取水口的底泥、周边土壤有机物的芳香度均很低(SUVA254(即比紫外吸光值)2),与腐殖质(Sigma)相比,底泥、土壤有机物不是氯消毒中THMs的重要前驱物,但却是HANs特别是HNMs的重要前驱物.相比氯消毒,氯胺消毒能大幅降低土壤、底泥有机物THMs、HKs、HANs、HNMs的生成量,而且也可抑制含溴DBPs的形成.臭氧预处理大幅提高了氯、氯胺消毒中HKs、HNMs的产量,但对THMs、HANs则不一定.太湖、钱塘江的土壤、底泥存在一定的溴污染,但不管是哪种消毒方式,均是HNMs的溴嵌入因子最大.     

Halogen-specific total organic halogen analysis: Assessment by recovery of total bromine

Determination of halogen-specific total organic halogen(TOX) is vital for studies of disinfection of waters containing bromide, since total organic bromine(TOBr) is likely to be more problematic than total organic chlorine. Here, we present further halogen-specific TOX method optimisation and validation, focusing on measurement of TOBr. The optimised halogen-specific TOX method was validated based on the recovery of model compounds covering different classes of disinfection by-products(haloacetic acids, haloacetonitriles,halophenols and halogenated benzenes) and the recovery of total bromine(mass balance of TOBr and bromide concentrations) during disinfection of waters containing dissolved organic matter and bromide. The validation of a halogen-specific TOX method based on the mass balance of total bromine has not previously been reported. Very good recoveries of organic halogen from all model compounds were obtained, indicating high or complete conversion of all organic halogen in the model compound solution through to halide in the absorber solution for ion chromatography analysis. The method was also successfully applied to monitor conversion of bromide to TOBr in a groundwater treatment plant. An excellent recovery(101%)of total bromine was observed from the raw water to the post-chlorination stage. Excellent recoveries of total bromine(92%–95%) were also obtained from chlorination of a synthetic water containing dissolved organic matter and bromide, demonstrating the validity of the halogen-specific TOX method for TOBr measurement. The halogen-specific TOX method is an important tool to monitor and better understand the formation of halogenated organic compounds, in particular brominated organic compounds, in drinking water systems.     

高温水解-溴离子选择电极测定煤中溴的影响因素实验研究

建立了高温水解-溴离子选择电极法测定煤中溴含量的方法,优选并确定高温水解提取煤中溴的最佳条件:煤样取样量0.80 g、高温水解温度1 100 ℃、停留时间25 min、氧气流量为0.2 L/min、水蒸气通量为0.9 m L/min、吸收液为10 g/L的Na OH溶液。研究表明在此优化条件下吸收液中的溴全部以Br-形式存在,用离子选择电极法测定消解液中Br-的量时,选择TISAB总离子强度调节缓冲溶液作为本方法的离子强度调节剂,测试温度为25 ℃、响应时间约为1 min。在此条件下,用岩石标准样进行验证,多次测定其误差均在标样规定的误差限内。本方法可消除试剂的基质效应和管道记忆效应,与其他方法相比,具有经济、简便和不需要贵重仪器等优点,因而能广泛用于煤和其它地质样品中溴含量的日常分析。     

ACUTE RESIDUAL TOXICITY OF SEVERAL WASTEWATER DISINFECTANTS TO AQUATIC LIFE1

ABSTRACT: This study was conducted to determine the comparative acute toxicity of chlorine, bromine chloride and ozone in wastewater, and to determine any acute toxicity associated with chlorinated wastewater which had been dechlorinated with sulfur dioxide. Toxicity tests were conducted with several species of cyprinids, salmonids and centrarchids, and the freshwater macroinvertebrate, Daphnia magna. Chlorinated effluent exhibited the greatest potential for residual toxicity of any disinfected stream tested. The reduced residual toxicity of chlorobrominated or ozonated effluent was largely the result of the more rapid dissipation of these disinfectants in wastewater. The acute residual toxicity of chlorinated effluent was eliminated by dechlorination with sulfur dioxide.     

Atmospheric lead and bromine in Germany: post-abatement levels,variabilities and trends

INTENTION, GOAL, SCOPE, BACKGROUND: Abatement measures since the 1970s have depleted lead and bromine levels in the atmosphere over large parts of Europe. Our knowledge of the atmospheric cycling of these elements while a several decade-long period of intensive mobilization reaches its end is incomplete. OBJECTIVE: We have characterized the trends in the atmospheric levels of Pb and Br and present-day temporal and spatial variabilities. METHODS: This was achieved by short-term (weeks) and long-term (years) measurements of particulate Pb and Br at various sites in Germany. Samples of atmospheric particulate matter were collected on filter membranes and analyzed by x-ray fluorescence. RESULTS AND DISCUSSION: Average Pb levels at rural and urban inland sites did not exceed concentrations in background aerosols, sampled at a Baltic Sea coastal site, by more than a factor of 3. Due to sea salt, bromide inland particulate Br levels are below those at a coastal site. There, non-sea salt Br, however, is significant as well. Urban Pb and Br levels are not necessarily higher than rural levels. The concentration levels have decreased in such a way that the previously common source, local vehicular traffic emissions, is no longer predominant. Regional rather than local sources have been increasingly determining the concentrations since the 1990s. This is more pronounced for Br than for Pb. We found indications for coal burning and long-range transport as significant Pb sources. For particulate Pb species, a range of ages (elapsed time since Pb emission) has been found. This range shows two maxima corresponding to characteristic times of 72 and 24 h. CONCLUSIONS: The (mean) atmospheric residence time of particulate Pb is longer than the residence time of Br, in particular in the wintertime. The chemical species contributing to atmospheric Pb should be addressed in future studies. RECOMMENDATION AND OUTLOOK: Clearly, despite effective abatement measures, atmospheric Pb will continue to be dominated by anthropogenic mobilization. The influence from long-range transport can be expected to decrease with the effectiveness of abatement programmes in neighbouring countries of the region.     

Monitoring long-term variation of aerosol composition: a dual particle-size approach applied to Hong Kong

The 1990's time series in Hong Kong for various components oftotal suspended particulate matter (TSP) and PM₁₀ have beenanalyzed in order to assess two distinct types of anthropogenicinput. The first of these relates to the immense reclamation andconstruction activities for new developments and airportconstruction. The concentrations of crustal components inPM₁₀ (= TSP – PM₁₀) were found to peak at the time ofthis maximum activity. A second type of anthropogenic input,ambient lead from petrol vehicles, has decreased in Hong Kongand now represents a regional background. Ambient bromine nowarises mainly from the seasalt source.     

Geochemical mapping in Jamaica

A high-precision regional geochemical data base of Jamaica is being developed as a basis for a wide variety of economic and environmental applications. These include pollution studies, resource identification and management, agriculture, land use, and the relationship between geochemistry and the health of crops, animals, and man. The acquisition of analytical data is mainly by instrumental neutron activation analysis using a SLOWPOKE reactor and by energy dispersive X-ray fluorescence. Concentration ranges and means in soil are presented for 31 elements and maps illustrating the distributions of Al, Br, Co, and the -ray intensities are presented as examples. Compared with world averages the levels of many heavy metals in Jamaican soils are found to be relatively high and in the main strongly correlated with bauxite occurrences. The high content of bromine in the soils appears to reflect the impact of sea-spray.     

溴掺杂TiO_2光催化剂的制备与性能研究

以KBr和Ti(SO4)2为原料,通过水热法制备了高催化活性的溴掺杂纳米TiO2(Br-TiO2)光催化剂,利用XRD、XPS、TEM、BET和UV-Vis DRS等测试手段对其进行了表征。通过苯酚降解实验评价了Br-TiO2的光催化活性。结果表明,700℃焙烧、溴与钛的摩尔比为0.35∶1时,Br-TiO2具有最佳光催化活性。该催化剂为晶体发育完整的锐钛矿相TiO2,粒径平均大小为50 nm,比表面积为16.81 m2/g,在紫外区的吸收得到加强,光催化能力优于Degussa P-25。确定了降解苯酚的最佳条件:催化剂投加量为0.5 g/L,苯酚初始浓度为10 mg/L,pH值为6.0。     

铜绿微囊藻胞内物消毒副产物生成：氯化和溴化比较

为了研究蓝藻水华期间释放的有机物给原水水质及给水处理过程带来的影响,选取优势藻种铜绿微囊藻的胞内物质(IOM)作为前驱体,分析了其结构特征.此外,分别研究了IOM在pH 6.5、7.1及8.4条件下与氯及溴反应后性质的变化及消毒副产物的生成,并进行了相关性分析.结果表明,IOM中以相对分子质量较大的组分(>30×103)为主,其溶解性有机碳(DOC)含量占总量的68.8%.三维荧光光谱(EEM)的结果表明IOM的成分主要以芳香蛋白类物质为主,其单位DOC的荧光强度为92.6 AU·L·mg-1.与氯或溴反应后,芳香蛋白类EEM峰值下降了76.6%~93.3%,且其降低值与三卤甲烷(THMs,R2=0.81)和卤乙酸(HAAs,R2=0.77)的生成量正相关.IOM与氯或溴反应生成的THMs和HAAs浓度均随着pH的增加而增加.溴相比氯与IOM反应可以生成更多的THMs和HAAs,且HAAs的卤代程度更高,但是氯及溴与IOM反应能力的差异随着pH的升高而逐渐减小,即k OBr·IOM/k OCl·IOM相似文献