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Heavy metals and surfactants have a significant effect on the sorption of organic contaminants. In this study, batch equilibrium experiments were carried out to investigate the influence of Pb(NO(3))(2) on the sorption of p-nitrophenol (PNP) onto sediments in the presence of cationic surfactant cetylpyridinium chloride (CPC). Results indicated that in the complex system containing PNP, Pb(NO(3))(2) and CPC, the sorption of PNP decreased with increasing concentration of Pb(NO(3))(2) due primarily to competing for adsorption sites. Likewise, partitioning of PNP in adsorbed surfactant layers and micelles decreased with increasing level of Pb(NO(3))(2). Moreover, the influence of different metal ions (Pb(2+), Cd(2+), Zn(2+)) was examined and results indicated that the presence of heavy metals inhibited the sorption of PNP in the order: Pb(2+)>Cd(2+)>Zn(2+). The competitive effect of the heavy metals was in agreement with the hydration energy and hydrated radius. The results are believed to provide a useful insight into describing the transport and fate of PNP in natural environments. 相似文献
214.
Luo J Weber FA Cirpka OA Wu WM Nyman JL Carley J Jardine PM Criddle CS Kitanidis PK 《Journal of contaminant hydrology》2007,92(1-2):129-148
We present a travel-time based reactive transport model to simulate an in-situ bioremediation experiment for demonstrating enhanced bioreduction of uranium(VI). The model considers aquatic equilibrium chemistry of uranium and other groundwater constituents, uranium sorption and precipitation, and the microbial reduction of nitrate, sulfate and U(VI). Kinetic sorption/desorption of U(VI) is characterized by mass transfer between stagnant micro-pores and mobile flow zones. The model describes the succession of terminal electron accepting processes and the growth and decay of sulfate-reducing bacteria, concurrent with the enzymatic reduction of aqueous U(VI) species. The effective U(VI) reduction rate and sorption site distributions are determined by fitting the model simulation to an in-situ experiment at Oak Ridge, TN. Results show that (1) the presence of nitrate inhibits U(VI) reduction at the site; (2) the fitted effective rate of in-situ U(VI) reduction is much smaller than the values reported for laboratory experiments; (3) U(VI) sorption/desorption, which affects U(VI) bioavailability at the site, is strongly controlled by kinetics; (4) both pH and bicarbonate concentration significantly influence the sorption/desorption of U(VI), which therefore cannot be characterized by empirical isotherms; and (5) calcium-uranyl-carbonate complexes significantly influence the model performance of U(VI) reduction. 相似文献
215.
Mechanism of decolorization and degradation of CI Direct Red 23 by ozonation combined with sonolysis
The decolorization and degradation of CI Direct Red 23, which is suspected to be carcinogenic, were investigated using ozonation combined with sonolysis. The results showed that the combination of ozonation and sonolysis was a highly effective way to remove color from waste water. The operational parameters, namely concentration of the dye, pH, ozone dose and ultrasonic density, were investigated during the process. The decolorization of the dye followed pseudo-first-order kinetics. Increasing the initial concentration of Direct Red 23 led to a decreasing rate constant. The optimum pH for the reaction was 8.0, and both lower and higher pH decreased the removal rate. The effect of the ozone dose on the dye decolorization was much greater than that of the sonolysis density. Intermediates such as naphthalene-2-sulfonic acid, 1-naphthol, urea and acetamide were detected by gas chromatography coupled with mass spectrometry in the absence of pH buffer, while nitrate and sulfate ions and formic, acetic and oxalic acids were detected by ion chromatography. A tentative degradation pathway was proposed without any further quantitative analyses. During the degradation, all nitrogen atoms and phenyl groups of Direct Red 23 were degraded into urea, nitrate ion, nitrogen and formic, acetic and oxalic acids, etc. 相似文献
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Comparative on Causes and Accumulation of Selenium in the Tree-rings Ambient High-selenium Coal Combustion Area from Yutangba, Hubei, China 总被引:1,自引:0,他引:1
Liu G Zhang Y Qi C Zheng L Chen Y Peng Z 《Environmental monitoring and assessment》2007,133(1-3):99-103
Toxic trace elements emitted during coal combustion are the main sources of air pollution. They are released into the atmosphere
mainly in the forms of fine ash, smoke and flue, and thus adversely affect plant, animal and human health. Selenium is one
of toxic and the most volatile in coal. Large amount of atmospheric emission of selenium, as well as selenium present and
scrubber stockpiles in ash may create serious environmental problems. In the paper, on the basis of investigating the abundance
and distribution of selenium in plant-rings during recent 20 years, the bioaccumulation of selenium is explained that selenium
in plant, which were collected from the village of selenium-rich coal combustion, is much higher than that in plants collected
away from the village of selenium-rich coal combustion. The main origins of selenium are selenium-rich coal combustion and
high-selenium rock weathered. The selenium recycle by food chain and selenium will accumulate and redistribute in environments. 相似文献
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生物滤池对气相与液相中污染物质的净化 总被引:4,自引:0,他引:4
通过实验室研究探讨了生物滤池同时处理废水和废气的可行性。试验结果表明:在25℃-37℃条件下,甲苯废气的流量为90L/h,甲苯浓度为500mg/m^3;废水的流量为0.4L/h,CODcr浓度为400-750mg/L,甲苯与CODcr的去除率分别是70%-72%和86%-89%。 相似文献
220.
垃圾填埋场稳定化及其研究现状 总被引:19,自引:0,他引:19
文章对直埋场稳定化过程进行了初步描述,并从填埋气、渗滤液、垃圾组成和沉降等4个方面总结了填埋场稳定化的研究现状。 相似文献