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31.
用超细玻璃纤维滤膜采集杭州市某道路上机动车排放的苯并(a)芘,经超声萃取,高速离心后直接进HPLC分析。在选定的色谱条件下,苯并(a)芘与其他多环芳烃完全分离,绝对进样量在0.8~0.02 ng时线性良好,相关系数为0.99979,最小检出量0.8 pg,加标回收率87.5%~93.8%。 相似文献
32.
Adsorption of Pb(II) on variable charge soils amended with rice-straw derived biochar 总被引:11,自引:0,他引:11
Two Ultisols and one Oxisol from tropical regions of southern China were incubated with rice straw biochar to investigate the effect of biochar on their surface charge and Pb(II) adsorption using batch methods. The incorporation of biochar induced a remarkable increase in soil cation exchange capacity after 30 d of incubation. The incorporation of biochar significantly increased the adsorption of Pb(II) by these variable charge soils; the enhancement of adsorption of Pb(II) by these soils increased with the addition level of biochar. Adsorption of Pb(II) involved both electrostatic and non-electrostatic mechanisms; however, biochar mainly increased Pb(II) adsorption through the non-electrostatic mechanism via the formation of surface complexes between Pb2+ and functional groups on biochar. There was greater enhancement of biochar on the non-electrostatic adsorption of Pb(II) by the variable charge soils at relatively low pH. Therefore, the incorporation of biochar decreased the activity and availability of Pb(II) to plants through increased non-electrostatic adsorption of Pb(II) by acidic variable charge soils. 相似文献
33.
34.
Effective EU and Member State policies for stimulating CCS 总被引:1,自引:0,他引:1
Although CO2 capture and storage (CCS) is widely recognised as an option to mitigate climate change, consistent and effective EU policies to advance CCS are still absent. This paper discusses policy instruments for advancing large-scale deployment of CCS in the European Union, and evaluates them in a multi-criteria analysis. The EU Emissions Trading Scheme (EU-ETS) is a cost-effective instrument for limiting greenhouse gas emissions, but it is questionable whether its currently limited time horizon and short-trading periods will lead to substantial CCS diffusion. Complementary policies at the EU and the Member State level may repair this and provide sufficient incentives for CCS. Potential policies include financial instruments such as investment subsidies, a feed-in scheme, or a CO2 price guarantee, as well as a CCS mandate or a low-carbon portfolio. These policy options differ with respect to their environmental effectiveness, possible interaction with the EU-ETS, costs and financial risk involved, and their competition with other mitigation options. Interactions between Member State policies and the EU-ETS are smaller in scope than those of EU-wide policies, but they are more likely to lead to displacement of financial resources from other low-carbon technologies. In addition, national policies may pose a significant part of the financial risk of CCS operations with Member States, reducing the operator's incentive to innovate. Overall, structural policies at the EU level, such as a mandate or a low-carbon portfolio standard would be more conducive for realising large-scale deployment of CCS across the EU as well as more acceptable to environmental organisations. 相似文献
35.
Banerjee A Nayak D Chakrabortty D Lahiri S 《Environmental pollution (Barking, Essex : 1987)》2008,151(2):423-427
Attempt has been made to study the accumulation behaviour of a common plant, Mung bean (Vigna radiata) towards Cr(III) and Cr(VI) to have an insight on the migration and bio-magnification of Cr. For this purpose healthy germinated Mung bean seeds were sown in the sand in the presence of Hoagland's nutrient solution containing measured amount of K(2)(51)Cr(2)O(7) and (51)Cr(NO(3))(3).9H(2)O. Growth rate was also studied in the presence and absence of phosphate salts in the medium. It has been found that the transfer of chromium from soil to plant is significantly low (maximum 5% for both Cr(III) and Cr(VI)). Maximum accumulation of Cr occurs in the root with respect to the total chromium accumulation by the plant. Other parts of the Mung bean plant, e.g. cotyledons, shoot and leaves, show negligible accumulation. Therefore, the chance of direct intake of Cr through food as well as through the grazing animals to human body is less. 相似文献
36.
Comparison of China’s Environmental Impact Assessment (EIA) Law with the European Union (EU) EIA Directive 总被引:1,自引:0,他引:1
In this paper, we first review the development of China’s Environmental Impact Assessment (EIA) system in the past 30 years.
Then we compare the framework and operational procedures of China’s new EIA law with those of the EU EIA Directive. We also
compare public participation, as well as sanctions and control in the two EIA systems. In addition, we identify where the
processes in both EIA systems are similar or different from one another. By comparison, we noted that there are at least three
obvious weaknesses in China’s EIA system: (1) the application of new models for EIA legislation; (2) the improvement of EIA
guidance and education; and (3) the enhancement of public participation in EIA process. Our study indicates that these three
major shortcomings should be overcome and improved in China’s EIA system, when compared with the EU EIA system. 相似文献
37.
Isobe T Takada H Kanai M Tsutsumi S Isobe KO Boonyatumanond R Zakaria MP 《Environmental monitoring and assessment》2007,135(1-3):423-440
A comprehensive monitoring survey for polycyclic aromatic hydrocarbons (PAHs) and phenolic endocrine disrupting chemicals
(EDCs) utilizing mussels as sentinel organisms was conducted in South and Southeast Asia as a part of the Asian Mussel Watch
project. Green mussel (Perna viridis) samples collected from a total of 48 locations in India, Indonesia, Singapore, Malaysia, Thailand, Cambodia, Vietnam, and
the Philippines during 1994–1999 were analyzed for PAHs, EDCs including nonylphenol (NP), octylphenol (OP) and bisphenol A
(BPA), and linear alkylbenzenes (LABs) as molecular markers for sewage. Concentrations of NP ranged from 18 to 643 ng/g-dry
tissue. The highest levels of NP in Malaysia, Singapore, the Philippines, and Indonesia were comparable to those observed
in Tokyo Bay. Elevated concentrations of EDCs were not observed in Vietnam and Cambodia, probably due to the lower extent
of industrialization in these regions. No consistent relationship between concentrations of phenolic EDCs and LABs were found,
suggesting that sewage is not a major source of EDCs. Concentrations of PAHs ranged from 11 to 1,133 ng/g-dry, which were
categorized as “low to moderate” levels of pollution. The ratio of methylphenanthrenes to phenanthrene (MP/P ratio) was >1.0
in 20 out of 25 locations, indicating extensive input of petrogenic PAHs. This study provides a bench-mark for data on the
distribution of anthropogenic contaminants in this region, which is essential in evaluating temporal and spatial variation
and effect of future regulatory measures. 相似文献
38.
Lemly AD 《Environmental monitoring and assessment》2007,125(1-3):361-375
This paper gives step-by-step instructions for assessing aquatic selenium hazards associated with mining. The procedure was
developed to provide the U.S. Forest Service with a proactive capability for determining the risk of selenium pollution when
it reviews mine permit applications in accordance with the National Environmental Policy Act (NEPA). The procedural framework
is constructed in a decision-tree format in order to guide users through the various steps, provide a logical sequence for
completing individual tasks, and identify key decision points. There are five major components designed to gather information
on operational parameters of the proposed mine as well as key aspects of the physical, chemical, and biological environment
surrounding it — geological assessment, mine operation assessment, hydrological assessment, biological assessment, and hazard
assessment. Validation tests conducted at three mines where selenium pollution has occurred confirmed that the procedure will
accurately predict ecological risks. In each case, it correctly identified and quantified selenium hazard, and indicated the
steps needed to reduce this hazard to an acceptable level. By utilizing the procedure, NEPA workers can be confident in their
ability to understand the risk of aquatic selenium pollution and take appropriate action. Although the procedure was developed
for the Forest Service it should also be useful to other federal land management agencies that conduct NEPA assessments, as
well as regulatory agencies responsible for issuing coal mining permits under the authority of the Surface Mining Control
and Reclamation Act (SMCRA) and associated Section 401 water quality certification under the Clean Water Act. Mining companies
will also benefit from the application of this procedure because priority selenium sources can be identified in relation to
specific mine operating parameters. The procedure will reveal the point(s) at which there is a need to modify operating conditions
to meet environmental quality goals. By recognizing concerns early in the NEPA process, it may be possible for a mining company
to match operational parameters with environmental requirements, thereby increasing the likelihood that the permit application
will be approved. 相似文献
39.
Samaratunga SS Nishimoto J Tabata M 《Environmental science and pollution research international》2008,15(1):27-30
BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples. 相似文献
40.
制备了聚硅酸氯化铝(PASC)絮凝剂,并用其进行了皂素废水处理实验。考察了絮凝剂投加量、pH值、搅拌速度对COD和浊度去除率的影响。结果表明,当絮凝剂投加量为9~13.5 mg/L、pH值5~7、搅拌速度150~250 r/min时,COD和浊度去除效果较好。最佳工艺条件为:絮凝剂投加量11.25 mg/L、pH值6、搅拌速度200 r/min。此时,COD去除率为93.7%,浊度去除率为97.5%。PASC的絮凝性能明显优于PAC。 相似文献