Pulsed discharge plasma induced Fenton-like reactions for the enhancement of the degradation of 4-chlorophenol in water

To sufficiently utilize chemically active species and enhance the degradation rate and removal efficiency of toxic and biorefractory organic pollutant para-chlorophenol (para-CP), the introductions of iron metal ions (Fe²⁺/Fe³⁺) into either pulsed discharge plasma (PDP) process or the PDP process with TiO₂ photo-catalyst were tentatively performed. The experimental results showed that under the same experimental condition, the degradation rate and removal efficiency of para-CP were greatly enhanced by the introduction of iron ions (Fe²⁺/Fe³⁺) into the PDP process. Moreover, when iron ions and TiO₂ were added together in the PDP process, the degradation rate and removal energy of para-CP further improved. The possible mechanism was discussed that the obvious promoting effects were attributed to ferrous ions via plasma induced Fenton-like reactions by UV light irradiation excited and hydrogen peroxide formed in pulsed electrical discharge, resulting in a larger amount of hydroxyl radicals produced from the residual hydrogen peroxide. In addition, the regeneration of ferric ions to ferrous ions facilitates the progress of plasma induced Fenton-like reactions by photo-catalytic reduction of UV light, photo-catalytic reduction on TiO₂ surface and electron transfer of quinone intermediates, i.e. 1,4-hydroquinone and 1,4-benzoquinone.     

Biomonitoring spatial and temporal impact of atmospheric dust from a cement industry

The objective of this work was to evaluate the spatial and temporal impact of dust-pollution in the vicinity of a cement industry, located in an area with dry climate. The spatial impact integrated over time was evaluated from the concentrations of Ca, Fe and Mg in in-situ Xanthoria parietina. The temporal pattern was assessed through one-month transplants of the lichen Ramalina canariensis. Four potential sources of atmospheric dust were evaluated: the limestone-quarry; the unpaved roads, the deposit area and the cement mill. Calcium concentration in lichens was considered the best cement-dust indicator. Different types of dust (clinker and grinded-limestone-dust) resulted in different time-patterns of Ca accumulation, which was also related with the different influence that wet and dry periods have in the lichen accumulation process. The dust pollution was found to be deposited locally and dependent on: the nature of dust particles and the volume and frequency of precipitation.     

Magnetic anomalies of forest soils in the Upper Silesia-Northern Moravia region

Previous investigations revealed a strong magnetic anomaly due to soil magnetic enhancement in the industrialized cross-border area of Upper Silesia (Poland) and Northern Moravia (Czech Republic). Since industrial and urban dusts contain magnetic particles, this soil magnetic enhancement is assumed to be of anthropogenic origin, caused by a high concentration of atmospherically deposited magnetic particles, accumulated in topsoil layers. This assumption is proved by investigations of vertical profiles of magnetic susceptibility along a transect crossing the border area of the two countries. The results show that the population of magnetic minerals in the organic horizon is different from that in the mineral horizons. The vertical distribution of magnetic susceptibility and thermomagnetic analysis suggests negligible lithogenic contribution. The observed relationship between magnetic susceptibility and some heavy metals, confirmed by micromorphological observations and microchemical analysis of magnetic particles separated from the organic horizons of forest topsoil, has proved the usefulness of soil magnetometry for pollution study.     

Volatile pollutants emitted from selected liquid household products

BACKGROUND, AIM, AND SCOPE: To identify household products that may be potential sources of indoor air pollution, the chemical composition emitted from the products should be surveyed. Although this kind of survey has been conducted by certain research groups in Western Europe and the USA, there is still limited information in scientific literature. Moreover, chemical components and their proportions of household products are suspected to be different with different manufacturers. Consequently, the current study evaluated the emission composition for 42 liquid household products sold in Korea, focusing on five product classes (deodorizers, household cleaners, color removers, pesticides, and polishes). MATERIALS AND METHODS: The present study included two phase experiments. First, the chemical components and their proportions in household products were determined using a gas chromatograph and mass spectrometer system. For the 19 target compounds screened by the first phase of the experiment and other selection criteria, the second phase was done to identify their proportions in the purged-gas phase. RESULTS: The number of chemicals in the household products surveyed ranged from 9 to 113. Eight (product class of pesticides) to 17 (product class of cleaning products) compounds were detected in the purged-gas phase of each product class. Several compounds were identified in more than one product class. Six chemicals (acetone, ethanol, limonene, perchloroethylene (PCE), phenol, and 1-propanol) were identified in all five product classes. There were 13 analytes occurring with a frequency of more than 10% in the household products: limonene (76.2%), ethanol (71.4%), PCE (66.7%), phenol (40.5%), 1-propanol (35.7%), decane (33%), acetone (28.6%), toluene (19.0%), 2-butoxy ethanol (16.7%), o-xylene (16.7%), chlorobenzene (14.3%), ethylbenzene (11.9%), and hexane (11.9%). All of the 42 household products analyzed were found to contain one or more of the 19 compounds. DISCUSSION: The chemical composition varied broadly along with the product classes or product categories, and it was different from that reported in other studies abroad, although certain target chemicals were identified in both studies. This finding supports an assertion that chemical components emitted from household products may be different in different products and with different manufacturers. The chlorinated pollutants identified in the present study have not been reported to be components of cleaning products in papers published since the early 1990s. Limonene was identified as having the highest occurrence in the household products in the present study, although it was not detected in any of 67 household products sold in the U.S. CONCLUSIONS: The emission composition of selected household products was successfully examined by purge-and-trap analysis. Along with other exposure information such as use pattern of household products and the indoor climate, this composition data can be used to estimate personal exposure levels of building occupants. This exposure data can be employed to link environmental exposure to health risk. It is noteworthy that many liquid household products sold in Korea emitted several toxic aromatic and chlorinated organic compounds. Moreover, the current finding suggests that product types and manufacturers should be considered, when evaluating building occupants' exposure to chemical components emitted from household products. RECOMMENDATIONS AND PERSPECTIVES: The current findings can provide valuable information for the semiquantitative estimation of the population inhalation exposure to these compounds in indoor environments and for the selection of safer household products. However, although the chemical composition is known, the emissions of household products might include compounds formed during the use of the product or compounds not identified as ingredients by this study. Accordingly, further studies are required, and testing must be done to determine the actual composition being emitted. Similar to eco-labeling of shampoos, shower gels, and foam baths proposed by a previous study, eco-labeling of other household products is suggested.     

烟花爆竹用氧化剂的研究进展

在调查研究的基础上,分析、总结、研讨用于烟花爆竹的氧化剂的历史、现状及发展方向。分析和讨论氯酸盐类、高氯酸盐类、硝酸盐类以及金属氧化物等氧化剂的物化性质、燃爆性能及各自用于烟火剂的优缺点。研究指出:将不同类型的氧化剂复合使用,当选择的组分及搭配的比例合适时,不仅能使各种氧化剂充分发挥其优点,而且还将产生一些新的实际的性能。同时提出:复合氧化剂是配制燃放效果好、安全性能高、价格低廉的烟花爆竹氧化剂的发展方向。     

A sulfur removal and disposal process through H2S adsorption and regeneration: Ammonia leaching regeneration

An iron oxide solid sponge H₂S adsorbent works by reacting H₂S and turning ferric oxide into ferric sulfide. The ferric sulfide will be converted back into ferric oxide and elemental sulfur when contacting oxygen or air. This study investigates the leaching of elemental sulfur from the solid sponge using anhydrous liquid ammonia as solvent. The leaching treatment expectedly results in effective regeneration of the adsorbent, which is able to lead to a sulfur removal and recovery process suitable for handling the small and mid-sized sulfur production cases, i.e., those less than 10 ton/day sulfur. The leaching does not significantly impair the physical properties, including the adsorbent pellet strength. The adsorption–regeneration (or leaching) cycle could be repeated at least three times. The cumulative sulfur loading can achieve as high as 50% (w/w), three times greater than that in the one-time use. The wash-off in leaching and the spent adsorbent can be made into slurry that is to be injected into underground formations such as depleted oil wells. It is anticipated that this underground injection is safer and more efficient than acid gas injection.     

Quantifying the importance of diffuse minewater pollution in a historically heavily coal mined catchment

There has been considerable progress in developing treatment systems for point sources of minewater pollution in recent years; however, there remains a knowledge gap in the characterisation and remediation of diffuse minewater sources. Data are presented from the River Gaunless catchment, a historically heavily coal mined catchment in the northeast of England. Instream iron (Fe) loadings were monitored alongside loadings arising from point minewater discharges over a 12-month period to assess the dynamic importance of diffuse sources of minewater pollution. In low flow, diffuse sources account for around 50% of instream loading, a proportion which increases to 98% in high flow conditions. The low flow sources appear to be dominated by direct discharge of contaminated groundwater to surface waters in lower reaches of the catchment. In high flow, resuspended Fe-rich sediments, which are both naturally occurring and derived from historic mining, become the dominant diffuse source of Fe in the water column.     

Group size and relative competitive ability: geometric progressions as a conceptual tool

Contrary to the assumptions of many previous theoretical models, group size has recently been shown in experiments to have an effect on the relative (as well as absolute) competitive abilities of group members. Here we introduce a novel and effective mathematical tool for describing how relative competitive ability will change for any two specified individuals within a group as group size changes. We show that there is no simple general rule for describing how relative competitive ability will change with group size. A subsequent empirical test of the model helps to illustrate that very specific knowledge of the system under study is needed in order to produce robust predictions. Received: 23 December 1998 / Received in revised form: 26 July 1999 / Accepted: 2 October 1999     

Enhanced reductive dechlorination of DDT in an anaerobic system of dissimilatory iron-reducing bacteria and iron oxide

The transformation of DDT was studied in an anaerobic system of dissimilatory iron-reducing bacteria (Shewanella decolorationis S12) and iron oxide (α-FeOOH). The results showed that S. decolorationis could reduce DDT into DDD, and DDT transformation rate was accelerated by the presence of α-FeOOH. DDD was observed as the primary transformation product, which was demonstrated to be transformed in the abiotic system of Fe²⁺ + α-FeOOH and the system of DIRB + α-FeOOH. The intermediates of DDMS and DBP were detected after 9 months, likely suggesting that reductive dechlorination was the main dechlorination pathway of DDT in the iron-reducing system. The enhanced reductive dechlorination of DDT was mainly due to biogenic Fe(II) sorbed on the surface of α-FeOOH, which can serve as a mediator for the transformation of DDT. This study demonstrated the important role of DIRB and iron oxide on DDT and DDD transformation under anaerobic iron-reducing environments.     

Arsenic in groundwater and sediment in the Mekong River delta, Vietnam

A study of groundwater and sediment during 2007-2008 in the Mekong River delta in Vietnam (MDVN) revealed that 26%, 74%, and 50% of groundwater samples were above the US EPA drinking water guidelines for As (10 μg/L), Mn (0.05 mg/L), and Fe (0.3 mg/L). The range of As, Fe, and Mn concentrations in the MDVN were <0.1-1351 μg/L, <0.01-38 mg/L, and <0.01−14 mg/L, respectively. Elevated levels of As were found in groundwater at sampling sites close to the Mekong River and in wells less than 60−70 m deep. An inverse relationship was found between As and Mn concentrations in groundwater. Sediment samples from An Giang and Dong Thap had the highest As concentrations (18 mg/kg and 38 mg/kg, respectively). Arsenic sediment occurred mainly in the poorly crystalline Fe oxide phases. Reductive dissolution of the Fe oxide phase is not necessarily the dominant mechanism of As release to groundwater.