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331.
通过亚铵法制浆蒸煮黑液直接作农肥施于水稻田的研究,给出了不同施肥方式连续数天田间水和渗滤水中黑液污染物变化情况,定量描述了黑液作肥料直接施于水稻田对水环境的影响。 相似文献
332.
An air quality monitoring network (AQMN) usually performs the basic function of assessment of regional air quality and demonstration of compliance with ambient air quality standards in an urban area. Different pollutants, however, may present different characteristic variabilities due to their specific emission patterns, rates of diffusion, and transport and transformation behaviors. But the costs of siting in a pollutant-specific monitoring network would be higher than that for a common network with respect to several pollutants monitored simultaneously. This paper presents a survey of multi-pollutant design principles and optimal searches for siting patterns of an AQMN using both simulation and optimization models as a combined tool. While conservative, quasi-stable, and reactive pollutants are considered in the design principles, cost, coverage effectiveness, and spatial correlation characteristics are included in the multi-criteria decision making process. For illustrative purpose, a series of technical settings and two types of objectives were examined in the case study for the city of Kaohsiung in Taiwan. 相似文献
333.
H. S. Lin H. D. Scott K. F. Steele H. I. Inyang 《Environmental monitoring and assessment》1999,58(2):151-172
Statistical methods and a Geographic Information System (GIS) were used to investigate potential indicators of ground water vulnerability to agricultural chemical contamination in a representative area of the Mississippi River alluvial aquifer. A total of 47 wells were sampled for analysis of nitrate, phosphorus, potassium, and 13 pesticides commonly-used in the area. Ten soil and hydrogeologic variables and five ground water vulnerability indices were examined to explain the variations of chemical concentrations. The results showed that no individual soil or hydrogeologic variables or their linear combinations could explain more than 25% of the variation of the chemical concentrations. A quadratic response surface model with the values of confining unit thickness, slope, soil permeability, depth to ground water, and recharge rate accounted for 62% of the variation of nitrate, 43% of P, and 83% of K, suggesting that the interactions among soil and hydrogeologic variables were significant. Observed trends of decreasing nitrate and P concentrations with increasing well depth and/or depth to ground water seemed to correlate with carbonate equilibrium in the aquifer and more reduced environment with depth. In view of uncertainties involved, it was recognized that the limitations associated with input data resolution used in GIS and the formulation of leaching indices limited their use for predicting ground water vulnerability. Misuse of pesticides could be another factor that would complicate the relationships between pesticide concentrations and the vulnerability indices. 相似文献
334.
鉴于目前环境影响预测中基准值取法存在的问题,提出了结合目前通用做法与灰色预测的灰靶方案,该方案使得环境影响预测结果在一定范围内变化,从而更为切合评价实际。 相似文献
335.
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
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337.
超临界水氧化中设备腐蚀的研究现状 总被引:2,自引:0,他引:2
超临界水氧化(SCWO)技术是近年发展起来的处理有机难溶废物的安全高效的新技术。在阐述超临界水的物理、化学性质的基础上,介绍了SCWO反应的工作原理和流程,分析总结了世界范围内开展的SCWO环境中设备腐蚀及监测技术等方面的研究动态,提出了我国SCWO技术研究的未来发展方向。 相似文献
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