Method of removal of volatile organic compounds by using wet scrubber coupled with photo-Fenton reaction - Preventing emission of by-products

The photo-Fenton reaction was applied as a novel method for the removal of volatile organic compounds (VOCs) in the gas phase, and its effectiveness was experimentally examined. In conventional VOCs removal methods using a photocatalyst or ozone, VOCs are oxidized in the gas phase. Therefore, incompletely oxidized intermediates, which may have adverse effects on health, are likely to contaminate the treated air. On the other hand, in the VOCs removal method developed in this study, because the VOCs are oxidized in the liquid phase by the photo-Fenton reaction, any incompletely oxidized intermediates produced are confined to the liquid phase. As a result, the contamination of the treated air by these harmful intermediates can be prevented. Using a semi-batch process, it was found that the removal efficiency for toluene in a one-pass test (residence time of 17 s) was 61%, for an inlet toluene gas concentration of 930 ppbv, an initial iron ion concentration of 20 mg L⁻¹, and an initial hydrogen peroxide concentration of 630 mg L⁻¹. The removal efficiency was almost constant as long as H₂O₂ was present in the solution. Proton transfer reaction mass spectrometry analysis confirmed the absence of any incompletely oxidized intermediates in the treated air.     

Linking chemical elements in forest floor humus (Oh-horizon) in the Czech Republic to contamination sources

While terrestrial moss and other plants are frequently used for environmental mapping and monitoring projects, data on the regional geochemistry of humus are scarce. Humus, however, has a much larger life span than any plant material. It can be seen as the “environmental memory” of an area for at least the last 60-100 years. Here concentrations of 39 elements determined by ICP-MS and ICP AES, pH and ash content are presented for 259 samples of forest floor humus collected at an average sample density of 1 site/300 km² in the Czech Republic. The scale of anomalies linked to known contamination sources (e.g., lignite mining and burning, metallurgical industry, coal fired power plants, metal smelters) is documented and discussed versus natural processes influencing humus quality. Most maps indicate a local impact from individual contamination sources: often more detailed sampling than used here would be needed to differentiate between likely sources.     

Bioavailability of particulate metal to zebra mussels: biodynamic modelling shows that assimilation efficiencies are site-specific

This study investigates the ability of the biodynamic model to predict the trophic bioaccumulation of cadmium (Cd), chromium (Cr), copper (Cu), nickel (Ni) and zinc (Zn) in a freshwater bivalve. Zebra mussels were transplanted to three sites along the Seine River (France) and collected monthly for 11 months. Measurements of the metal body burdens in mussels were compared with the predictions from the biodynamic model. The exchangeable fraction of metal particles did not account for the bioavailability of particulate metals, since it did not capture the differences between sites. The assimilation efficiency (AE) parameter is necessary to take into account biotic factors influencing particulate metal bioavailability. The biodynamic model, applied with AEs from the literature, overestimated the measured concentrations in zebra mussels, the extent of overestimation being site-specific. Therefore, an original methodology was proposed for in situ AE measurements for each site and metal.     

Chemistry of fogs at Agra, India: Influence of soil particulates and atmospheric gases

Fog water samples were collected in the months of December and January during 1998–2000 at Agra, India. The samples were analyzed for pH, major anions (F⁻, Cl⁻, SO₄ ²⁻, NO₃ ⁻, HCOO⁻ and CH₃COO⁻), major cations (Ca²⁺, Mg²⁺, Na⁺ and K⁺) and NH₄ ⁺ using ion chromatography, ICP-AES and spectrophotometer methods, respectively. pH of fog water samples ranged between 7.0 and 7.6 with a volume weighted mean of 7.2, indicating its alkaline characteristic. NH₄ ⁺ contributed 40%, SO₄ ²⁻ and NO₃ ⁻ accounted for 28%, while Ca²⁺, Mg²⁺, Na⁺ and K⁺ accounted for 16% of the total ionic concentration. The ratios of Mg²⁺/Ca²⁺ and Na⁺/Ca²⁺ in fog water indicates that 50–75% of fog water samples correspond to the respective ratios in local soil. Significant correlation between Ca²⁺, Mg²⁺, Na⁺ and K⁺ suggests their soil origin. The order of neutralization, NH₄ ⁺ (1.4) > Ca²⁺ (0.28) > Mg²⁺ (0.12), indicates that NH₄ ⁺ is the major neutralizing species. Fog water and atmospheric alkalinity were also computed and were found to be 873 and 903 neqm⁻³, respectively. Both of these values are higher than values reported from temperate sites and thus indicate that at the present level of pollutants, there is no risk of acid fog problem. The study also shows that the alkaline nature of fog water is due to dissolution of ammonia gas and partly due to interaction of fog water with soil derived aerosols.     

Characteristics and applications of controlled-release KMnO4 for groundwater remediation

In situ chemical oxidation (ISCO) using potassium permanganate (KMnO4) has been widely used as a practical approach for remediation of groundwater contaminated by chlorinated solvents like trichloroethylene. The most common applications are active flushing schemes, which target the destruction of some contaminant source by injecting concentrated permanganate (MnO4(-)) solution into the subsurface over a short period of time. Despite many promising results, KMnO4 flushing is often frustrated by inefficiency associated with pore plugging by MnO2 and bypassing. Opportunities exist for the development of new ISCO systems based on KMnO4. The new scheme described in this paper uses controlled-release KMnO4 (CRP) as an active component in the well-based reactive barrier system. This scheme operates to control spreading of a dissolved contaminant plume. Prototype CRP was manufactured by dispersing fine KMnO4 granules in liquid crystal polymer resin matrix. Scanning electron microscope data verified the formation of micro-scale (ID=20-200 microm) secondary capillary permeability through which MnO4(-) is released by a reaction-diffusion process. Column and numerical simulation data indicated that the CRP could deliver MnO4(-) in a controlled manner for several years without replenishment. A proof-of-concept flow-tank experiment and model simulations suggested that the CRP scheme could potentially be developed as a practical approach for in situ remediation of contaminated aquifers. This scheme may be suitable for remediation of sites where accessibility is limited or some low-concentration contaminant plume is extensive. Development of delivery systems that can facilitate lateral spreading and mixing of MnO4(-) with the contaminant plume is warranted.     

垃圾渗滤液处理中膜污染的防治

膜污染及其防治是影响膜系统运行效果的重要因素.对运行1年多的利用膜技术的垃圾渗滤液处理工程进行了研究,从预处理、膜污染结构与形态、膜清洗等方面,探讨了防治膜污染的措施.研究表明,调整进水pH、过滤、添加阻垢剂等预处理措施可减缓膜污染的发生;膜面污染层的主要成分是有机物,并含有Al、Si等的胶体物质以及Fe和Ca的化合物;先碱洗后酸洗的清洗效果好于先酸洗后碱洗.工程中采用先碱洗后酸洗的措施是可行的,清洗后产水量由13.8 L/(m2·h)提高至17.0 L/(m2·h),产水电导率由117 μS/cm降至45μS/cm,进水压力由4.60 MPa降至3.40 MPa.     

有关化工石化建设项目环境风险评价技术评估的探讨

根据国家化工石化行业建设项目加强环境风险评价的主要规定,结合化工石化行业建设项目特点及环境影响技术评估,反思化工石化项目评价及评估工作,重点从环境风险评价方面,对进一步完善环境风险评价与防范的后评估,从严建设项目技术评估与环境管理等进行了初步探讨,目的是为建设项目环境影响技术评估和环境管理提供参考。     

化学需氧量现有2种标准分析方法若干问题研究

《水质化学需氧量的测定重铬酸盐法》(HJ 828-2017)和《高氯废水化学需氧量的测定氯气校正法》(HJ/T70-2001)是测定水中CODCr现有有效的2种标准方法.针对这2种方法存在的问题,通过实验给出操作建议.指出,对高氯废水稀释后采用《HJ828-2017》方法测定水中CODCr时,稀释倍数太大或稀释后COD...     

Mating expenditures reduced via female sex pheromone modulation in the primitively eusocial halictine bee, Lasioglossum (Evylaeus) malachurum (Hymenoptera: Halictidae)

The present paper reports on behavioral experiments and gas chromatographic analysis of chemical communication in the mating biology of the primitively eusocial sweat bee Lasioglossum (Evylaeus) malachurum. In a dual-choice experiment, a female made odorless was significantly less attractive than an untreated one. Attraction in L. (Evylaeus) malachurum is therefore mediated by a female-produced sex pheromone. Further bioassays showed that unmated gynes are more attractive to males than mated ones. Males are able to differentiate between the two groups of females as little as 3 h after mating. Biotests with different samples obtained from attractive gynes showed surface extracts to be most attractive. Behavioral tests with synthetic copies of the compounds identified as cuticular constituents of virgin gynes were highly attractive to males; the volatile bouquets consisting of n-alkanes, n-alkenes and iso- pentenyl esters of unsaturated fatty acids were the most attractive samples. Isopentenyl esters of unsaturated fatty acids were the key compounds in inducing male inspections as well as stimulating pounces and copulatory attempts. Virgin and nesting gynes differed clearly in the relative and absolute amounts of the volatiles on the cuticle. The total amount of volatiles was significantly higher in virgin gynes and decreased in breeding queens. Hydrocarbons were the dominant group of compounds in both groups of females. The relative amounts of the wax-type ester, hexadecyl oleate, iso- pentenyl esters, and a hitherto unidentified steroid were higher in attractive virgin gynes, while the relative proportions of hydrocarbons and lactones dominated in nesting queens. The site of sex pheromone production in attractive young L. (Evylaeus) malachurum gynes remains unknown. Head glands or Dufour's gland secretions may be involved. Another possible source of the `active principle' found among the cuticular lipids could be glandular cells of the epidermis. The significance of modulation of female sex pheromone composition is discussed in terms of a reduction in mating expenditures. Received: 30 April 1998 / Accepted after revision: 24 July 1998