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61.
62.
Zerbinati O Pittavino S 《Environmental science and pollution research international》2003,10(6):395-398
BACKGROUND AND INTENTION: Aromatic sulphonates other than surfactants and their hydroxy and amino-derivatives are important intermediates for the production of azo dyes. Their production on a large scale can be detrimental for the environment, if the by-products of their synthesis are not disposed of appropriately. An industrial waste, the organic components of which were mainly amino and hydroxy-substituted aromatic sulphonates, seriously endangers the environment close to an dismissed Italian industrial site. Inorganic sulphates and chlorides contained in the waste seriously hinder its disposal by incineration, since they corrode furnace walls. In this work, preliminary exploration of aqueous-phase electrochemically and photochemically induced oxidation techniques have been performed as possible alternatives to incineration. METHODS: Electrochemically-induced oxidation was experimented on individual aromatic sulphonates and on an industrial waste by electrolysing them between smooth platinum electrodes at low temperature (5 degrees C) and high current densities (0.4 A/cm2) with aqueous 0.5 M NaHSO4 electrolyte. Photochemically-induced oxidation was performed by irradiating individual aromatic sulphonates or industrial waste with a 500 W mercury lamp in the presence of sodium peroxydisulphate. RESULTS AND DISCUSSION: After 200 min electrodegradation, 90% of the original compounds disappeared, while 50% Total Organic Carbon (TOC) of an industrial waste was removed from solution after 10 hours. After 180 min UV-photodegradation, 90% of two test aromatic sulphonates disappeared, while 65% of TOC of industrial waste was removed after 5 hours. CONCLUSIONS: Two methods, electrochemical and UV-persulphate oxidation of an industrial waste, were used in order to propose a disposal procedure alternative to incineration. Electrodegradation with smooth Pt anode in 0.5 M NaHSO4 at 5 degrees C halved TOC concentration within 10 hours, while persulphate-assisted UV-photochemical oxidation with a 500 W high pressure Hg lamp abated two-thirds of TOC concentration after 5 hours. Energetic consumption of electrodegradation was 0.33 kWh/g TOC, while that of photooxidation was larger than 2 kWh/g TOC. Although both techniques can be considered efficient from a purely chemical point of view, since both are capable of wet-oxidising the aromatic sulphonates and the industrial waste, electrodegradation seems more promising than a photochemical degradation if economical considerations are also taken into account. Considering also that neither cell design nor catalyst were optimised in this preliminary study, the energy yield of electrodegradation seems likely to be largely improved. 相似文献
63.
Raja S Ravikrishna R Kommalapati RR Valsaraj KT 《Environmental monitoring and assessment》2005,110(1-3):99-120
Seventeen fog events were sampled in Baton Rouge, Louisiana during 2002–2004 as part of characterizing wet deposition by fogwater
in the heavily industrialized corridor along the Louisiana Gulf Coast in the United States. These samples were analyzed for
chemical characteristics such as pH, conductivity, total organic and inorganic carbon, total metals and the principal ion
concentrations. The dominant ionic species in all samples were NH4+, NO3−, Cl− and SO42−. The pH of the fogwater sampled had a mean value of 6.7 with two cases of acidic pH of 4.7. Rainwater and fogwater pH were
similar in this region. The acidity of fogwater was a result of NO3− but partly offset by high NH4+. The measured gaseous SO2 accounted for a small percentage of the observed sulfate concentration, indicating additional gas-to-particle conversion
of SO2 to sulfate in fogwater. The gaseous NOx accounted for most of the dissolved nitrate and nitrite concentration in fogwater. The high chloride concentration was attributable
to the degradation of chlorinated organics in the atmosphere. The metal composition was traced directly to soil-derived aerosol
precursors in the air. The major metals observed in fogwater were Na, K, Ca, Fe, Al, Mg and Zn. Of these Na, K, Ca and Mg
were predominant with mean concentrations > 100 μM. Al, Fe and Zn were present in the samples, at mean concentrations < 100
μM. Small concentrations of Mn (7.8 μM), Cu (2 μM), Pb (0.07 μM) and As (0.32 μM) were also observed in the fogwaters, and
these were shown to result from particulates (PM2.5) in the atmosphere. The contribution to both ions and metals from the marine sources in the Louisiana Gulf Coast was minimal.
The concentrations of all principal ionic species and metals in fogwater were 1–2 orders of magnitude larger than in rainwater.
Several linear alkane organic compounds were observed in the fogwater, representing the contributions from petroleum products
at concentrations far exceeding their aqueous solubility. A pesticide (atrazine) was also observed in fogwater, representing
the contribution from the agricultural activities nearby. 相似文献
64.
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66.
Maria Grazia Gnoni Gianni Mummolo Luigi Ranieri 《Journal of Environmental Planning and Management》2008,51(6):833-845
In this paper, the authors propose a mixed integer linear programming model for designing an Integrated Solid Waste Management System (ISWMS) to meet specific economic goals. The model refers to a set of municipalities, known as ‘local basin’, which have to share a common waste management system. At the municipal level the model allows for an identification of the optimal collection service option; at the local basin level, the model provides the optimal waste flow appropriate to the collection service option of each municipality. The model has been applied to a full-scale case study of an area located in southeast Italy. A scenario analysis was carried out to investigate alternative municipal solid waste management options, which fundamentally differ in the organic flow mass rate to be either collected and composted or landfilled. Findings show that an increase in the cost of landfilling determines the optimal collection scenario and the configuration plants tend to recover higher rates of organics in separate collection and thus higher refuse derived fuel productions. The results obtained validate the application of the model in both the strategic planning and operational phases, by supporting public administrators at both municipality and local basin level in decision making and evaluation of technical and economic performances of ISWMSs. 相似文献
67.
进行了添加乙醇作为碳源强化油制气废水生物降解的研究,并利用GC/MS分析对油制气废水中芳烃类化合物的降解进行了初步研究。研究表明,共代谢基质乙醇的加入,可使菌种S-2、Y-3、XH-3、M-3对COD、氨氮、可萃取有机物等指标的去除率分别提高17.6%~25.6%、34.9%~42.8%、10.4%~14.2%;但在所采用的时间范围内,酚类化合物的去除率降低;芳烃类化合物的去除率提高15.4%~21.2%。除了维持无共代谢条件下对芳环数≤3的芳烃类化合物的良好降解能力外,对芳环数为4~6的化合物降解能力也有所提高。 相似文献
68.
Antony A Bassendeh M Richardson D Aquilina S Hodgkinson A Law I Leslie G 《Chemosphere》2012,86(8):829-836
Granular activated carbon (GAC) exhaustion rates on pulp and paper effluent from South East Australia were found to be a factor of three higher (3.62 cf. 1.47 kg m−3) on Kraft mills compared to mills using Thermomechanical pulping supplemented by Recycled Fibre (TMP/RCF). Biological waste treatment at both mills resulted in a final effluent COD of 240 mg L−1. The dissolved organic carbon (DOC) was only 1.2 times higher in the Kraft effluent (70 vs. 58 mg L−1), however, GAC treatment of Kraft and TMP/RCF effluent was largely different on the DOC persisted after biological treatment. The molecular mass (636 vs. 534 g mol−1) and aromaticity (5.35 vs. 4.67 L mg−1 m−1) of humic substances (HS) were slightly higher in the Kraft effluent. The HS aromaticity was decreased by a factor of 1.0 L mg−1 m−1 in both Kraft and TMP/RCF effluent. The molecular mass of the Kraft effluent increased by 50 g mol−1 while the molecular mass of the TMP/RCF effluent was essentially unchanged after GAC treatment; the DOC removal efficiency of the GAC on Kraft effluent was biased towards the low molecular weight humic compounds. The rapid adsorption of this fraction, coupled with the slightly higher aromaticity of the humic components resulted in early breakthrough on the Kraft effluent. Fluorescence excitation-emission matrix analysis of the each GAC treated effluent indicated that the refractory components were higher molecular weight humics on the Kraft effluent and protein-like compounds on the TMP/RCF effluent. Although the GAC exhaustion rates are too high for an effective DOC removal option for biologically treated pulp and paper mill effluents, the study indicates that advanced organic characterisation techniques can be used to diagnose GAC performance on complex effluents with comparable bulk DOC and COD loads. 相似文献
69.
Rocío Reina Christiane Liers Juan Antonio Ocampo Inmaculada García-Romera Elisabet Aranda 《Chemosphere》2013
The in vivo conversion of dry olive mill residue (DOR) by wood- and dung-dwelling fungi − Auricularia auricula-judae, Bjerkandera adusta and Coprinellus radians − increases peroxidase secretion up to 3.2–3.5-fold (∼1.3, 3.5 and 7.0 U g−1 DOR for dye-decolorizing peroxidase, manganese peroxidase and aromatic peroxygenases, respectively). The incubation of DOR with these fungi produced a sharp decrease in total phenolic content (100% within 4 wk), a reduction in phytotoxicity as well as a certain degree of plant growth caused by the stimulating effect of fungal-treated DOR. These findings correlate with a characteristic shift in the fragmentation pattern of water-soluble aromatics (detected at 280 nm) from low (0.2, 1.5 and 2.2 kDa, respectively) to high molecular mass (35 to >200 kDa), which demonstrates the presence of a polymerization process. Phenol-rich agricultural residues are a useful tool for enzyme expression and production studies of peroxidase-producing Agaricomycetes which could make DOR a valuable organic fertilizer. 相似文献
70.
杭州市居室空气中芳香族化合物污染现状及其来源解析 总被引:3,自引:0,他引:3
用热解吸/气质联用技术研究了杭州市居室空气中芳香族化合物的组成。结果表明,杭州市居室空气中共存在60种芳香族化合物,其中苯系化合物48种,非苯芳香族化合物12种,检出率大于50%的23种;苯、甲苯、乙苯、苯乙烯、邻二甲苯、间(对)-二甲苯等10种化合物的总含量之和大于85.39%,是室内空气中主要的芳香族污染物,除萘外,其他22种污染物的平均浓度值均随装修时间间隔延长而降低;污染物主要来源是室内装修过程中使用的或装修材料中残留的有机溶剂、机动车辆排放的尾气、居民家庭中常用的清洁用品及含萘等成分的防蛀剂。 相似文献