Volatile halogenated organics in swimming pools

This survey undertaken in Greece (Mytilene town) has shown that Volatile halogenated organics (VHO) are present in swimming pool water. Analysis was performed by purge‐and‐trap (PAT) gas chromatographic (GC) technique and samples from two public indoor swimming pools in Mytilene were analyzed for VHO. Water samples were collected every week for a period of three months, and have shown the occurrence of chloroform, dichlorobromomethane, chlorodi‐bromomethane, bromoform (all four are trihalomethanes [THMs]), as a result of the chlorination and the occurrence of tetrachloroethylene and 1,1,1,2‐tetrachloroethane is assigned to their introduction as impurities during the process treatment of water. The levels of concentrations ranged from 4.0 to 26.0 μg/1 for chloroform, from 0.26 to 7.0 μg/1 for dichlorobromomethane, from 0.5 to 3.0 μg/1 for chlorodibromomethane, from 0.07 to 0.9 μg/1 for bromoform, from no detectable levels to 0.07 μg/1 for tetrachloroethylene and from no detectable levels to 0.2 μg/1 for 1,1,1,2‐tetrachloroethane.     

Assessing inter-laboratory comparability and limits of determination for the analysis of cyclic volatile methyl siloxanes in whole Rainbow Trout (Oncorhynchus mykiss)

Cyclic volatile methyl siloxanes (cVMS) are high volume production chemicals used in a wide range of industrial and consumer products. Three cVMS compounds (D4, D5, and D6) have and are undergoing environmental risk evaluations in several countries and have been proposed for legal regulation in Canada. As interest in monitoring concentrations of these chemicals in the environment increase, there is a need to evaluate the analytical procedures for cVMS in biological matrices in order to assess the quality of data produced. The purpose of this study was to determine laboratory testing performance for measuring residues of D4, D5, and D6 in a standard set of fish homogenate samples and to estimate limits of determination for each substance. The samples sent to each laboratory consisted of homogenized whole body tissues of hatchery raised rainbow trout which were fed food fortified with D4, D5, and D6 (dosed) and trout that were fed standard food rations (control). The participants analyzed each sample using their analytical method of choice using their own standards and procedures for quantification and quality control. With a few exceptions, participating laboratories generated comparable results for D4, D5, and D6 in both the dosed and control samples having z-scores between 2 and −2. Method detection limits for the whole fish matrix were on average 2.4 ng g⁻¹ ww for D4, 2.3 ng g⁻¹ ww for D5, and 1.8 ng g⁻¹ ww for D6.     

椰壳活性炭吸附消除VOCs

对一种椰壳活性炭对甲基丙烯酸甲酯的吸附消除行为进行了研究,重点考察了甲基丙烯酸甲酯的浓度、流速和吸附温度等条件以及水汽存在时对活性炭吸附行为的影响。结果表明,该颗粒活性炭对甲基丙烯酸甲酯有良好的吸附效果,甲基丙烯酸甲酯进口浓度和进气量的改变均会影响吸附饱和时间,导致其增加或减少。通过变温吸附实验确定降低环境温度对其吸附有促进作用。湿度为50%时吸附量相对干气饱和吸附量影响较小,说明该活性炭抗水汽能力较好。经多次重复再生实验,其饱和吸附量未见明显下降。     

活性炭吸附和脱附-等离子体氧化净化有机废气的研究

根据滑动弧放电等离子体适于降解高浓度有机物废气的特性,结合活性炭吸附法,提出了吸附器的吸附浓缩和热脱附-等离子体氧化净化有机废气的方法。在活性炭吸附过程中,最初2 h内甲苯净化率达到100%,随着时间的增加净化率下降;在热脱附滑动弧放电等离子体净化过程中,甲苯降解效率最高为97.3%。将滑动弧放电等离子体反应器出口气相产物收集进行FT-IR检测,发现放电后有CO2、CO、H2O和NO2产生,并分析了甲苯的降解机理。     

Determination and potential importance of diterpene (kaur-16-ene) emitted from dominant coniferous trees in Japan

Reactive volatile organic compounds (VOCs) are known to affect atmospheric chemistry. Biogenic VOCs (BVOCs) have a significant impact on regional air quality due to their large emission rates and high reactivities. Diterpenes (most particularly, kaur-16-ene) were detected in all of the 205 enclosure air samples collected over multiple seasons at two different sites from Cryptomeria japonica and Chamaecyparis obtusa trees, the dominant coniferous trees in Japan,. The emission rate of kaur-16-ene, was determined to be from 0.01 to 7.1 μg dwg⁻¹ h⁻¹ (average: 0.61 μg dwg⁻¹ h⁻¹) employing branch enclosure measurements using adsorbent sampling followed by solid phase-liquid extraction techniques. The emission rate was comparable to that of monoterpenes, which is known major BVOC emissions, collected from the same branches. In addition, total emission of kaur-16-ene at 30 °C was estimated to exceed that of total anthropogenic VOC emissions.     

MUNICIPAL RESPONSES TO VOLATILE ORGANIC COMPOUNDS IN WISCONSIN GROUND WATER1

ABSTRACT: Contamination of ground water supplies with volatile organic compounds is a new and significant problem. Municipalities and their community water systems are often the first to discover ground water contamination because of the monitoring programs they are required to carry out. When contamination exceeds standards, some action is required. The responses of Wisconsin municipalities to volatile organic compounds that exceed standards in their ground water sources is described. Actions to protect human health are prompt, but the survey results indicate plumes of contaminated ground water are usually not treated. They may continue to migrate and contaminate other private and public wells.     

用生物滴滤床处理H2S和挥发性有机物混合废气

用生物滴滤床（BTF）处理某化工厂污水站的H2S和挥发性有机物（VOCs）混合废气，当废气中H2S质量浓度为120～400mg／m^3、VOCs质量浓度为115～340mg／m^时，运行稳定后H2S和VOCs的去除率为95％和85％。考察了影响BTF运行的循环水水质情况，试验结果表明：加入Na2CO3可使循环水pH控制在3～6；循环水中含盐量、Cl^-质量浓度和SO4^2-质量浓度分别为2200～3300，600～800，1200～1400mg／L，均未达到抑制微生物的水平。     

Contamination of Oxygen-Consuming Organics in the Yellow River of China

Contamination of oxygen-consuming organics (OCOs) was one of the most serious problems in the Yellow River of China. This study was conducted to analyze monitoring of the data on OCOs contamination for the river in 1980 and during 1992–1999 as well as examining the effect of suspended solids (SS) on chemical oxygen demand (COD_Mn) and biochemical oxygen demand (BOD₅) of river water. Several significant results have arisen from the study. First, COD_Mn and BOD₅ of the river water showed an increasing trend from the upper to the lower reaches of the mainstream. BOD₅ values of river water in 1992 were significantly higher than those in 1980 and showed an increasing trend during 1992–1999. Second, OCOs in river water of the mainstream was attributed mainly to point sources; the ratio of point to non-point sources of BOD₅ was about 2.81. The load from point sources showed an increasing trend during 1992–1998. In contrast, the load from non-point sources manifested a decreasing trend during this period; this was caused by the decreasing trend of SS content in river water. The total load of BOD₅ from point and non-point sources displayed an increasing trend during 1992–1998. Third, as the humic substances in SS can hardly be biologically oxidized in natural conditions but can be oxidized by chemical oxidants such as potassium permanganate, COD_Mn was not suitable for being regarded as a parameter reflecting the pollution degree of OCOs in river water with a high SS content.     

强化混凝工艺深度处理给水厂排泥废水

水厂废水的综合处理与回用是我国供水行业的新趋势和节水目标所在,采用强化混凝技术进行水厂排泥废水的深度处理。通过混凝剂筛选实验和有机物表征确定最佳混凝剂为高效聚合铝(HPAC),适宜投加量为650 mg/L。当混凝剂HPAC投加量为650 mg/L时,对COD、TOC、浊度和色度的去除率分别为82.5%、89.8%、95%和92.5%,相应的出水值分别为58 mg/L、8.46 mg/L、2.35 NTU、13度,COD满足《污水综合排放标准》(GB 8978-1996)的要求(COD≤100 mg/L),同时实验结果显示聚合氯化铝(PAC)、HPAC、三氯化铁(FeCl3)主要去除分子量处于>1 300 Da范围的有机物,对分子量处于744～1 300 Da之间的有机物去除有限。     

Biogenic volatile organic compound analyses by PTR-TOF-MS: Calibration, humidity effect and reduced electric field dependency

Green leaf volatiles(GLVs) emitted by plants after stress or damage induction are a major part of biogenic volatile organic compounds(BVOCs). Proton transfer reaction time-of-flight mass spectrometry(PTR-TOF-MS) is a high-resolution and sensitive technique for in situ GLV analyses, while its performance is dramatically influenced by humidity, electric field,etc. In this study the influence of gas humidity and the effect of reduced field(E/N) were examined in addition to measuring calibration curves for the GLVs. Calibration curves measured for seven of the GLVs in dry air were linear, with sensitivities ranging from 5 to10 ncps/ppbv(normalized counts per second/parts per billion by volume). The sensitivities for most GLV analyses were found to increase by between 20% and 35% when the humidity of the sample gas was raised from 0% to 70% relative humidity(RH) at 21°C, with the exception of(E)-2-hexenol. Product ion branching ratios were also affected by humidity,with the relative abundance of the protonated molecular ions and higher mass fragment ions increasing with humidity. The effect of reduced field(E/N) on the fragmentation of GLVs was examined in the drift tube of the PTR-TOF-MS. The structurally similar GLVs are acutely susceptible to fragmentation following ionization and the fragmentation patterns are highly dependent on E/N. Overall the measured fragmentation patterns contain sufficient information to permit at least partial separation and identification of the isomeric GLVs by looking at differences in their fragmentation patterns at high and low E/N.