Continuous, intermittent and passive sampling of airborne VOCs

Long sampling periods are often advantageous or required for measuring air quality and characterizing exposures. However, sampling periods exceeding 8 to 24 h using thermally desorbable adsorbent tube (TDT) samplers for the measurement of airborne volatile organic compounds (VOCs) face several challenges, including maintaining stable and low flow rates, and avoiding breakthrough of the adsorbent. These problems may be avoided using intermittent sampling; however, the literature contains few if any reports that have evaluated this technique in environmental, occupational or other applications. The purpose of this study is to evaluate continuous, intermittent and passive sampling methods using both laboratory and real-world tests. Laboratory tests compared continuous and intermittent (active) samplers in a controlled dynamic test gas generation system. Field tests used side-by-side active and passive samplers in an office, home workshop and four smokers' homes. All samples were analyzed for a wide range of VOCs by GC-MS. In most instances, intermittent sampling yielded better reproducibility (duplicate precision of 10 +/- 6%) than continuous low-flow sampling (18 +/- 5%), in part due to difficulty maintaining low flows. Concentrations obtained using intermittent sampling agreed with those for continuous sampling, with downward biases resulting primarily from errors in flow rate measurements. In the field, more VOC species were detected using active rather than passive sampling. Passive measurements were 12% lower than continuous measurements, a difference attributed to declining uptake rates at higher concentrations over the 3 to 4 d sampling period. Overall, most measurements obtained using the three sampling methods agreed within 20% for a wide range of concentrations (0.1 to 230 microg m(-3)). Both passive and intermittent sampling approaches are suitable for long sampling periods, but intermittent sampling provides greater flexibility with respect to sampling period, and permits the use of multi-bed adsorbents that can capture a wider range of VOCs.     

Application of a novel cold activated carbon fiber-solid phase microextraction for analysis of organochlorine pesticides in soil

A novel and simple analytical procedure using cold activated carbon fiber-solid phase microextraction (CACF-SPME) was applied to determine organochlorine pesticides (OCs) in soil samples. The pesticides in this study consist of alpha -, beta -, gamma -, and delta -hexachlorocyclohexane (HCH). By heating the sample while cooling the fiber, the developed method not only provides better performance in terms of sensitivity, linearity and recovery but also offers shorter adsorption procedure than that of traditional headspace-solid phase microextraction (HS-SPME). The experimental conditions such as the amount of water, adsorption time and adsorption temperature were optimized. Matrix effects were investigated with different types of soils. We concluded that using the standard addition method was required for quantification purposes. The limits of detection obtained using the proposed method range from 0.01 to 0.05 ng/g, and the recoveries for CACF-SPME are in the range of 80.01% to 89.68% with relative standard deviation (RSDs) better than 8.60%. The proposed method was further applied to determine OCs in real agricultural soil. The results are in good agreement with those obtained using traditional ultrasonic extraction. The research demonstrates the suitability of the CACF-SPME for the analysis of OCs in soil.     

Rapid determination of ETS markers with a prototype field-portable GC employing a microsensor array detector

The adaptation of a portable gas chromatograph (GC) prototype with several unique design features to the determination of vapor-phase markers of environmental tobacco smoke (ETS) is described. This instrument employs a dual-stage adsorbent preconcentrator, two series-coupled separation columns that can be independently temperature programmed, and a detector consisting of an array of nanoparticle-coated chemiresistors, whose response patterns are used together with retention times for vapor recognition. An adsorbent pre-trap was developed to remove semi-volatile organics from the sample stream. Conditions were established to quantitatively capture two ETS markers, 2,5-dimethylfuran (2,5-DMF) and 4-ethenylpyridine (4-EP, as a surrogate for 3-EP), and to separate them from the 34 most prominent co-contaminants present in ETS using ambient air as the carrier gas. A complete analysis can be performed every 15 min. Projected detection limits are 0.58 and 0.08 ppb for 2,5-DMF and 4-EP, respectively, assuming a 1 L sample volume, which are sufficiently low to determine these markers in typical smoking-permitted environments.     

淀山湖总氮和总磷的时空模拟分布

为了解氮磷在淀山湖的时空分布特征及变化规律,运用ELCOM-CAEDYM耦合模块分析了2008年淀山湖总氮和总磷浓度的时空变异。研究表明:模型较好地模拟了淀山湖上覆水中的总氮、总磷的时空分布,总氮、总磷质量浓度总体变化趋势与实测值相一致。淀山湖春冬季总氮的质量浓度要明显高于夏秋季,3月份是淀山湖总氮质量浓度最高的时候,千墩港是淀山湖总氮质量浓度最高的区域。淀山湖总磷的分布并未表现出季节上的规律性,空间分布整体呈现北高南低的趋势。     

新标准下环境空气质量监控网络完善实践 ——以珠三角地区佛山市为例

介绍珠三角及佛山市新标准监测网络结构,从拓宽网络有效覆盖范围、提升网络对污染研究的支撑能力、以及巩固数据实时发布工作基础等多角度分析了网络完善需求,提出了下一阶段网络建设的重点措施建议,并介绍了佛山市目前计划进行的网络完善工作。     

Phytoremediation of phenol using Polygonum orientale,including optimized conditions

Removing phenol from wastewater has become a major challenge of international concern. Phytoremediation is a novel and eco-friendly method and is attracting an increasing amount of attention for treating phenol in wastewater. We studied the ability of Polygonum orientale, which is frequently present around water bodies and in wetlands in China, to phytoremediate phenol. We determined the inhibition concentration for phenol on P. orientale using emergency toxicology experiments and morphological observations. Isothermal and kinetic models were created to assess the adsorption process involved in phenol removal. Comparison tests in sterile conditions demonstrated that metabolic removal was the main way in which the phenol concentrations were decreased, and removal by adsorption played a smaller role. An orthogonal test was performed to determine the optimum conditions under which P. orientale will remove phenol, and these were found to be an initial phenol concentration of 5 mg L^?1, 100 % natural light, and a 13-day treatment time. These results provide a theoretical basis for increasing our understanding of the mechanisms involved in the removal of phenol by P. orientale and will help in developing its application in the greening of urban areas to provide both phytoremediation and esthetic landscaping.     

异烟酸-巴比妥酸分光光度法测定水中总氰化物的探讨

对异烟酸-巴比妥酸分光光度法测定水中总氰化物的试验条件进行了探讨,分析了蒸馏时馏出液体积对结果的影响,明确了显色剂的配制及保存时效等问题。提出样品预蒸馏时可适当减少馏出液的收集体积,测定结果无显著性差异;将氯胺T、异烟酸-巴比妥酸试剂在冰箱中于4℃保存,在正常情况下可稳定使用4周。     

2-(2-喹啉偶氮)-4-二乙氨基苯甲酸光度法测定镍的研究

合成了新试剂 2 -( 2 -喹啉偶氮 ) -4 -二乙氨基苯甲酸 ( QADEABA) ,并研究了其与镍的显色反应 ,在 p H=8.0的硼酸 -磷酸二氢钾缓冲介质中 ,吐温 -80存在下 ,QADEABA与镍反应生成 2∶ 1稳定络合物 ,λmax=5 90 nm ,ε=1 .1 8× 1 0 5L· mol-1· cm-1。镍含量在 0～ 0 .4 mg/ L内符合比耳定律 ,方法用于水样中镍含量的测定 ,结果令人满意     

Emissions of reduced sulphur compounds from the surface of primary and secondary wastewater clarifiers at a Kraft Mill

Emissions of reduced sulphur compounds (RSCs) from the primary and secondary clarifiers at a Kraft mill were measured for respectively 8 and 22 days using a floating flux chamber. In the primary clarifier, dimethyl disulphide (DMDS) had the highest mean flux (0.83 microg s(-1) m(-2)) among all RSCs, and the mean flux of total reduced sulphur (TRS) was 1.53 microg s(-1) m(-2). At the secondary clarifier, dimethyl sulphide (DMS) had the highest mean flux (0.024 microg s(-1) m(-2)), and the mean flux of total reduced sulphur (TRS) was 0.025 microg s(-1) m(-2). Large variations in fluxes as a function of sampling date were observed in both clarifiers. Emission fluxes of DMS from the secondary clarifier were correlated with temperature in the flux chamber and with the biological and chemical oxygen demands (BOD and COD) of the wastewater. Emission rates of RSCs from the clarifiers were found to be insignificant by comparison with other mill sources.     

Evaluation of potential habitat with an integrated analysis of a spatial conservation strategy for David's deer, Elaphurus davidians

How to assess the potential habitat integrating landscape dynamics and population research, and how to reintroduce animals to potential habitats in environments highly human disturbed are still questions to be answered in conservation biology. According to behavioral research on Elaphurus davidians, we have developed a suitability index and a risk index to evaluate the potential habitats for the deer. With these indices, we conducted two transect assessments to evaluate the gradient change of the target region. Then, taking rivers as border lines, we tabulated the forest areas, high grassland area and total area and then compared the forest and high grassland area in each subregion. Furthermore, we computed the land use transfer matrix for the whole Yancheng coast during 1987-2000. We also computed human modified index (HMI) in six subregions. Lastly with a geographical information system support we obtained the spatial distribution of the indices and evaluation of the whole potential habitats from a neighborhood analysis. The transect assessment showed that the suitability of the coastal area was higher than that of the inland area for the deer, while the southern area was higher than the northern. Landscape metrics and HMI analysis showed that different landscape patterns and different anthropogenic disturbance existed within the region, and the increasing human disturbance was the key factor causing the pattern dynamics. The evaluation of potential habitats showed that there was an estimated carrying capacity of no more than 10,000 for David's deer reintroduction into the natural area. Also the reintroduction strategy was discussed. This integrated approach linked the population research and the landscape metrics, and the dataset with different scale; thus, it is an approach likely to be useful for the protection of other large animal in a landscape highly disturbed by humans.