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551.
Effect of natural organic matter on arsenic release from soils
and sediments into groundwater 总被引:6,自引:0,他引:6
Arsenic (As) contamination in groundwater has received significant attention recently. Natural and anthropogenic sources contribute to the worldwide occurrence of As contamination. As speciation is an important factor related to its toxic and mobile behavior. The release of As from soils and sediments into groundwater is governed by several geophysicochemical processes, of which, As sorption behavior is of principle significance. This review paper summarizes existing information regarding the effects of natural organic matter (NOM) on the fate and mobility of As species in the environment. NOM may enhance the release of As from soils and sediments into the soil solution, thereby facilitating As leaching into the groundwater. The main influencing mechanisms include competition for available adsorption sites, formation of aqueous complexes, and/or changes in the redox potential of site surfaces and As redox speciation. NOM may also serve as binding agents, thereby reducing As mobility. However, comparably little research has been performed on this aspect. Since most investigations have been done on purified minerals under laboratory conditions, further research involving various geological materials under natural environmental conditions is required. Development of proper geochemical conceptual models may provide means of predicting the role of NOM in arsenic leaching and/or immobilization. 相似文献
552.
The role of humic substances in chromium sorption onto natural organic matter (peat) 总被引:5,自引:0,他引:5
To elucidate mechanisms of Cr3+ sorption onto the unaltered solid natural organic matter, the comparative studies of this ion binding from a solution at pH 4.0 onto three selected particle size fractions: 2000–1000 μm, 630–200 μm and 63–20 μm of markedly different HS content and structure, separated by a wet sieving from an overall sample of peat (Brushwood Peat Humus) were carried out. Comparable patterns of COOH groups and CECt confirmed that for cation exchange capacity were responsible mainly cations connected with COO− functional groups. It was though found that aliphatic acids in the solid state did not take part in Cr3+ binding, thus the finest studied fraction 63–20 μm of the highest contents of functional groups showed the lowest sorption capacity for Cr3+, while similar patterns of sorbed Cr3+, soluble HS content and base CEC0 indicated that these parameters were directly interrelated. The base ion exchange processes determined by CEC0 (with Ca2+ as a predominant exchangeable cation) appeared to be not the major mechanisms responsible for Cr3+ sorption. For this metal, strong binding to insoluble large molecular weight organic pool two- to threefold prevailed over the ion exchange processes. Very low acid desorption indicated generally low mobility of Cr3+-organic compounds. 相似文献
553.
A/DAT-IAT生物膜法处理高含盐废水 总被引:1,自引:0,他引:1
以含盐量为60 000mg/L(以NaCl计)的模拟工业废水为研究对象,利用A/DAT-IAT生物膜反应器,研究A/DAT-IAT工艺对投加悬浮填料后高含盐废水的处理,并以CODCr、NH4 -N、PO43--P等作为指标评价处理效果.试验结果表明,在总水力停留时间(HRT)为13 h、pH=7,5、25℃条件下,进水ρ(CODCr)、ρ(NH4 -N)和ρ(PO43--P)分别为907.4~1 210.0 mg/L、86.2~99.7 mg/L和3.6~5.1 mg/L.CODCr、NH4 -N和PO43--P的平均去除率分别为73.9%、38.6%和93.5%,平均出水SS为198 mg/L,其中CODCr和PO43--P的去除效果较好.研究表明,A/DAT-IAT生物膜法较其他活性污泥法有了较大的提高. 相似文献
554.
Perfluorinated Surfactants in Surface and Drinking Waters (9 pp) 总被引:1,自引:0,他引:1
Skutlarek D Exner M Färber H 《Environmental science and pollution research international》2006,13(5):299-307
Background, Aim and Scope
In this paper recent results are provided of an investigation on the discovery of 12 perfluorinated surfactants (PS) in different
surface and drinking waters (Skutlarek et al. 2006 a, Skutlarek et al. 2006 b). In the last years, many studies have reported
ubiquitous distribution of this group of perfluorinated chemicals, especially perfluorooctane sulfonate (PFOS) and perfluorooctanoic
acid (PFOA) in the environment, particularly in wildlife animal and human samples (Giesy and Kannan 2001, Houde et al. 2006,
Prevedouros et al. 2006). Perfluorinated surfactants (e.g. PFOS and PFOA) have shown different potentials for reproductory
interference and carcinogenity in animal experiments as well as partly long half-lives in humans (Guruge et al. 2006, FSA
UK 2006a, FSA UK 2006b, 3M 2005, OECD 2002, Yao and Zhong 2005). They possess compound-dependent extreme recalcitrance against
microbiological and chemical degradation and, in addition, they show variable potentials for bioaccumulation in animals and
humans (Houde et al. 2006).
Materials and Methods:
Surface and drinking water samples were collected from different sampling sites:
- Surface waters: samples taken from the rivers Rhine, Ruhr, Moehne and some of their tributaries. Further samples were taken
from the Rhine-Herne-Canal and the Wesel-Datteln-Canal.
- Drinking waters: samples taken in public buildings of the Rhine-Ruhr area.
After sample clean-up and concentration by solid-phase extraction, the perfluorinated surfactants were determined using HPLC-MS/MS.
Results:
All measured concentrations (sum of seven mainly detected components) in the Rhine river and its main tributaries (mouths)
were determined below 100 ng/L. The Ruhr river (tributary of the Rhine) showed the highest concentration (94 ng/L), but with
a completely different pattern of components (PFOA as major component), as compared with the other tributaries and the Rhine
river. Further investigations along the Ruhr river showed remarkably high concentrations of PS in the upper reaches of the
Ruhr river and the Moehne river (tributary of the Ruhr) (Ruhr: up to 446 ng/L, Moehne: up to 4385 ng/L). The maximum concentration
of all drinking water samples taken in the Rhine-Ruhr area was determined at 598 ng/L with the major component PFOA (519 ng/L).
Discussion:
The surface water contaminations most likely stem from contaminated inorganic and organic waste materials (so-called 'Abfallgemisch').
This waste material was legally applied to several agricultural areas on the upper reaches of the Moehne. Perfluorinated surfactants
could be detected in some suchlike soil samples. They contaminated the river and the reservoir belonging to it, likely by
superficial run-off over several months or probably years. Downstream, dilution effects are held responsible for decreasing
concentrations of PS in surface waters of the Moehne and the Ruhr river. In analogy to the surface water samples, PS (major
component PFOA) can be determined in many drinking water samples of the Rhine-Ruhr area where the water supplies are mainly
based on bank filtration and artificial recharge.
Conclusions:
The concentrations found in drinking waters decreased with the concentrations of the corresponding raw water samples along
the flow direction of the Ruhr river (from east to west) and were not significantly different from surface water concentrations.
This indicates that perfluorinated surfactants are at present not successfully removed by water treatment steps.
Recommendations and Perspectives:
Because of their different problematic properties (persistence, mobility, toxicity, bioaccumulation), the concentrations of
specific perfluorinated surfactants and their precursors in drinking waters and food have to be minimised. Therefore, it is
of utmost importance to take the initiative to establish suitable legal regulations (limitations/ban) concerning the production
and use of these surfactants and their precursors. Furthermore, it is indispensable to protect water resources from these
compounds. A discussion on appropriate limit values in drinking water and foodstuffs is urgently needed. Concerning the assumed
soil contamination, the corresponding regulation (Bioabfall-Verordnung 1998 – Regulation on Organic Waste 1998) should be
extended to allow the control of relevant organic pollutants. 相似文献
555.
556.
厌氧-好氧活性污泥法处理高浓度甲醇废水 总被引:5,自引:0,他引:5
介绍了厌氧一好氧活性污泥法处理电管厂高浓度甲醇废水的动态试验结果。试验结果表明:该方法处理高浓度甲醇废水,可以克服甲醇废水厌氧处理容易酸化的问题.运行稳定.抗负荷冲击性强.处理效果良好。 相似文献
557.
558.
生物滴滤池净化二氯甲烷废气的实验研究 总被引:20,自引:4,他引:16
在φ50mm生物滴滤池内进行了二氯甲烷废气净化的实验研究.由工厂活性污泥经驯化培养得到菌种,进一步接种、在填料表面挂膜,接种和挂膜约需30d.滴滤池内装填聚丙烯散堆填料,废气和循环液在滴滤池内逆流操作,循环液pH值为7.0±0.5,温度维持在28.5±2℃的条件下,生物膜系统能较好地适应进口浓度的变化.在气体空床停留时间为15.7s、二氯甲烷进口浓度为0.7~3.12g/m3的范围内,去除效率为72.0%~99.1%.滴滤池中的酸性环境对二氯甲烷的降解具有明显抑制作用. 相似文献
559.
560.
微塑料对环境中有机污染物吸附解吸的研究进展 总被引:1,自引:0,他引:1
微塑料已成为新的全球性环境污染问题。作为强吸附剂,微塑料可以吸附共存的有机污染物,进而改变其环境行为和毒性;也可以通过解吸作用促进污染物在不同介质中的迁移。因而,微塑料与有机污染物的相互作用强度和机理是全面评估两者的环境风险和深度研究微塑料毒性机制的必要信息。目前微塑料研究处于快速发展的起始阶段,加之微塑料本身成分、粒径、表面风化情况的复杂性及共存有机污染物的多样性使两者的相互作用十分复杂,亟需理清微塑料吸附解吸作用的影响因素和相关机制。因而,本文详细综述了微塑料对有机污染物吸附解吸作用的研究进展,并着重从微塑料性质(成分、粒径和表面风化)、有机污染物性质和水环境介质性质方面探讨了吸附的影响因素和相互作用机制,希望为微塑料吸附有机污染物及吸附的后续影响研究提供借鉴与参考。 相似文献