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721.
Recycling of WEEE plastics: a review 总被引:1,自引:0,他引:1
Electric and electronic equipment (EEE) is swiftly growing in volume, level of sophistication, and diversity. Also, it evolves briskly, moved by innovation and technical change, and draws on numerous and at times rare resources. Waste EEE (WEEE) has evolved into an important societal problem. Recycling and treating WEEE implies occupational as well as environmental hazards that are still incompletely documented. Still, second hand EEE has been exported and treated in Africa, China, and India in a precarious informal context. In developed countries, EEE recycling has been sustained by a wide range of initiatives and motives, such as sustainability, creating jobs, and the value of precious or rare metals. Current EU Directives require a steep reduction of WEEE plastics (WEEP) going to landfill. Mechanical, thermal, and feedstock recycling of WEEP are analysed and some options confronted. Plastics recycling should be weighed against the eventual risks related to their hazardous ingredients, mainly legacy brominated fire retardants and heavy metals. Another paper is related to a somewhat similar problem, yet involving a different mix of plastics: recycling plastics from automotive shredder residue. 相似文献
722.
Carbon Sequestration Function of Check-Dams: A Case Study of the Loess Plateau in China 总被引:2,自引:0,他引:2
Check-dams are the most common structures for controlling soil erosion in the Loess Plateau. However, the effect of check-dams on carbon sequestration, along with sediment transport and deposition, has not been assessed over large areas. In this study, we evaluated the carbon sequestration function of check-dams in the Loess Plateau. The results indicate that there were approximately 11 000 check-dams distributed in the Loess Plateau, with an estimate of the amount of sediment of 21 × 109 m3 and a soil organic carbon storage amount of 0.945 Pg. Our study reveals that check-dams in the Loess Plateau not only conserve soil and water but also sequester carbon. 相似文献
723.
Physicochemical and biological quality of soil in hexavalent chromium-contaminated soils as affected by chemical and microbial remediation 总被引:1,自引:0,他引:1
Yingping Liao Xiaobo Min Zhihui Yang Liyuan Chai Shujuan Zhang Yangyang Wang 《Environmental science and pollution research international》2014,21(1):379-388
Chemical and microbial methods are the main remediation technologies for chromium-contaminated soil. These technologies have progressed rapidly in recent years; however, there is still a lack of methods for evaluating the chemical and biological quality of soil after different remediation technologies have been applied. In this paper, microbial remediation with indigenous bacteria and chemical remediation with ferrous sulphate were used for the remediation of soils contaminated with Cr(VI) at two levels (80 and 1,276 mg kg?1) through a column leaching experiment. After microbial remediation with indigenous bacteria, the average concentration of water-soluble Cr(VI) in the soils was reduced to less than 5.0 mg kg?1. Soil quality was evaluated based on 11 soil properties and the fuzzy comprehensive assessment method, including fuzzy mathematics and correlative analysis. The chemical fertility quality index was improved by one grade using microbial remediation with indigenous bacteria, and the biological fertility quality index increased by at least a factor of 6. Chemical remediation with ferrous sulphate, however, resulted in lower levels of available phosphorus, dehydrogenase, catalase and polyphenol oxidase. The result showed that microbial remediation with indigenous bacteria was more effective for remedying Cr(VI)-contaminated soils with high pH value than chemical remediation with ferrous sulphate. In addition, the fuzzy comprehensive evaluation method was proven to be a useful tool for monitoring the quality change in chromium-contaminated soils. 相似文献
724.
Xuetao Guo Chen Yang Yinai Wu Zhi Dang 《Environmental science and pollution research international》2014,21(4):2572-2580
As one of the widely used antibiotics in the world, the environmental risks of tylosin (TYL) received more and more attention. In order to assess its environmental fate and ecological effects accurately, it is necessary to understand the sorption properties of TYL on the soils/sediments. The sorption of TYL on goethite at different pH and ionic strength conditions were measured through a series of batch experiments and the sorption data of TYL were fitted by Freundlich and dual-mode sorption models. It was obvious that sorption was strongly dependent on pH and ionic strength. Sorption capacity of TYL increased as the pH increased and ionic strength decreased. The pH and ionic strength-dependent trends might be related with complexation between cationic/neutral TYL species and goethite. The sorption affinity of TYL on goethite decreased as ionic strength increased, which only occurred at higher TYL concentrations, suggested that inner complex might have dominated process at low concentrations and outer complex might occur at higher concentrations of TYL. Spectroscopic evidence indicated that tricarbonylamide and hydroxyl functional groups of TYL might be accounted for the sorption on mineral surfaces. The experimental data of TYL sorption could be fitted by surface complexation model (FITEQL), indicating that ≡FeOH with TYL interaction could be reasonably represented as a complex formation of a monoacid with discrete sites on goethite. The sorption mechanism of TYL might be related with surface complexation, electrostatic repulsion, and H-bounding on goethite. It should be noticed that the heterogeneous of sorption affinity of TYL on goethite at various environment to assess its environment risk. 相似文献
725.
Rui Wan Yuyin Yang Weimin Sun Zhao Wang Shuguang Xie 《Environmental science and pollution research international》2014,21(4):3175-3181
The objective of the present study was to investigate the impact of ammonia and nitrate nitrogen sources on simazine biodegradation by Arthrobacter sp. strain SD1 and the community structures of ammonia-oxidizing archaea (AOA) and bacteria (AOB) in non-agricultural soil. Soil microcosms with different treatments were constructed for herbicide biodegradation test. The relative abundance of the strain SD1 and the structures of AOA and AOB communities were assessed using quantitative PCR (q-PCR) and terminal restriction fragment length polymorphism (TRFLP), respectively. The co-existence of two inorganic nitrogen sources (ammonia and nitrate) had certain impact on simazine dissipation by the strain SD1. Bioaugmentation could induce a shift in the community structures of both AOA and AOB, but AOA were more responsive. Nitrogen application had significant impacts on AOA and AOB communities in bioaugmented soils. Moreover, in non-bioaugmented soil, the community structure of AOA, instead of AOB, could be quickly recovered after herbicide application. This study could add some new insights towards the impacts of nitrogen sources on s-triazine bioremediation and ammonia-oxidizing microorganisms in soil ecosystem. 相似文献
726.
Xiaoling Yang Jun Huang Kunlun Zhang Gang Yu Shubo Deng Bin Wang 《Environmental science and pollution research international》2014,21(6):4634-4642
Perfluorooctane sulfonate (PFOS), a widely used mist suppressant in hard chrome electroplating industry, has been listed in the Stockholm Convention for global ban. 6:2 Fluorotelomer sulfonate (6:2 FTS) acid and salts have been adopted as alternative products in the market, but no data about their abiotic degradation has been reported. In the present study, the degradability of 6:2 FTS potassium salt (6:2 FTS-K) was evaluated under various advanced oxidation processes, including ultraviolet (UV) irradiation, UV with hydrogen peroxide (H2O2), alkaline ozonation (O3, pH = 11), peroxone (O3/H2O2), and Fenton reagent oxidation (Fe2+/H2O2). UV/H2O2 was found to be the most effective approach, where the degradation of 6:2 FTS-K followed the pseudo-first-order kinetics. The intermediates were mainly shorter chain perfluoroalkyl carboxylic acid (C7 to C2), while sulfate (SO4 2?) and fluoride (F?) were found to be the final products. The high yields of SO4 2? and F? indicate that 6:2 FTS-K can be nearly completely desulfonated and defluorinated under UV/H2O2 condition. The degradation should firstly begin with the substitution of hydrogen atom by hydroxyl radicals, followed by desulfonation, carboxylation, and sequential “flake off” of CF2 unit. Compared with PFOS which is inert in most advanced oxidation processes, 6:2 FTS-K is more degradable as the alternative. 相似文献
727.
Zhiqiang Nie Qingqi Die Yufei Yang Zhenwu Tang Qi Wang Qifei Huang 《Environmental science and pollution research international》2014,21(13):7863-7875
Polychlorinated dibenzo-p-dioxin and dibenzofuran (PCDD/PCDF) were overall measured and compared in ambient air, water, soils, and sediments along the upper reaches of the Haihe River of North China, so as to evaluate their concentrations, profiles, and to understand the processes of gas–particle partitioning and air–water/soil exchange. The following results were obtained: (1) The average concentrations (toxic equivalents, TEQs) of 2,3,7,8-PCDD/PCDF in air, water, sediment, and soil samples were 4,855 fg/m3, 9.5 pg/L, 99.2 pg/g dry weight (dw), and 56.4 pg/g (203 fg TEQ/m3, 0.46 pg TEQ/L, 2.2 pg TEQ/g dw, and 1.3 pg TEQ/g, respectively), respectively. (2) Although OCDF, 1,2,3,4,6,7,8-HpCDF, OCDD, and 1,2,3,4,6,7,8-HpCDD were the dominant congeners among four environmental sinks, obvious discrepancies of these congener and homologue patterns of PCDD/PCDF were observed still. (3) Significant linear correlations for PCDD/PCDF were observed between the gas–particle partition coefficient (K p) and the subcooled liquid vapor pressure (P L 0) and octanol–air partition coefficient (K oa). (4) Fugacity fraction values of air–water exchange indicated that most of PCDD/PCDF homologues were dominated by net volatilization from water into air. The low-chlorinated PCDD/PCDF (tetra- to hexa-) presented a strong net volatilization from the soil into air, while high-chlorinated PCDD/PCDF (hepta- to octa-) were mainly close to equilibrium for air–soil exchange. 相似文献
728.
Haiying Lu Linzhang Yang Sadaf Shabbir Yonghong Wu 《Environmental science and pollution research international》2014,21(14):8782-8791
To explain the detailed process involved in phosphorus removal by periphyton, the periphyton dominated by photoautotrophic microorganisms was employed in this study to remove inorganic phosphorus (P i ) from wastewater, and the removal kinetics and isotherms were then evaluated for the P i removal process. Results showed that the periphyton was capable of effectively removing P i that could completely remove the P i in 24 h at an initial P i concentration of 13 mg P L?1. Furthermore, the P i removal process by the periphyton was dominated by adsorption at initial stage (~24 h), which involved physical mechanistic process. However, this P i adsorption process was significantly influenced by environmental conditions. This work provides an insight into the understanding of phosphorus adsorption by periphyton or similar microbial aggregates. Graphical Abstract
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729.
Distribution and ecological risk assessment of organochlorine pesticides in surface sediments from the East Lake,China 总被引:1,自引:0,他引:1
Xiaoyan Yun Yuyi Yang Minxia Liu Jun Wang 《Environmental science and pollution research international》2014,21(17):10368-10376
Organochlorine pesticides (OCPs) are ubiquitous pollutants, and their presence in urban lakes is a concern for human and ecological health. Surface sediments in the East Lake, China, were collected in winter 2012 and summer 2013 to investigate concentrations, distribution patterns, possible sources, and potential ecological risks of OCPs in this area. The total concentrations of 14 OCPs ranged from 6.3 to 400 ng g?1 dry weight (dw) with an average concentration of 79 ng g?1 dw. The mean values of hexachlorocyclohexanes (HCHs) (α-, β-, γ-, and δ-HCH) and dichlorodiphenyltrichloroethanes (DDTs) (p,p’-DDE, p,p’-DDD, and p,p’-DDT) were 36 and 7.6 ng g?1 dw, accounting for 45 and 10 % of the total OCPs, respectively. The concentrations of OCPs in sediment samples collected in winter were significantly higher than those in summer, especially the HCHs, of which in winter were two times greater than summer. Composition analyses indicated that DDTs and endosulfan were mainly from historical contribution. Historical use of technical HCH and new input of lindane were probably the source of HCHs in the East Lake. Most sampling sites of HCHs and DDTs were found to have the potential ecological risk based on levels specified in the sediment quality standards. 相似文献
730.
Yongduo Chen Yang Li Anna Zhu Yifan Huang Zhen Liu Keping Yan 《Environmental science and pollution research international》2014,21(16):9948-9958
The degradation of aqueous Rhodamine B (RhB) was examined using a dual-channel spark switch module designed to regulate the steepness of pulsed high voltage with microsecond rise time. Depending on the energy per pulse, a spark along the water surface (SPWS) or streamer along the water surface (STWS) was formed. STWS was found to have a better degradation effect and energy efficiency toward RhB than SPWS at the same power; however, addition of H2O2 amounts resulted in increased degradation, the effect being more pronounced using SPWS. The initial concentration of RhB also appeared to influence the rate constant of the degradation reaction. Furthermore, TiO2 films doped with Fe, Mn, and Ce were found to enhance the degradation performance of plasma. A possible reaction mechanism of plasma formation along the water surface was concluded by determination of the main inorganic products in the liquid and gas phases. 相似文献