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城市污水处理厂除臭技术 总被引:10,自引:0,他引:10
介绍了城市污水处理厂臭气来源、成分及产量。针对目前国内外除臭技术的研究和发展情况,分析了污水处理厂的各种物理、化学和生物除臭方法的技术原理、优缺点和应用现状。结合日本城市污水处理厂的运行实际,重点介绍了一种不产生臭气的新技术——腐殖活性污泥法的工艺流程、特点及其应用现状。 相似文献
955.
Leaching of bisphenol A (BPA) to seawater from polycarbonate plastic and its degradation by reactive oxygen species 总被引:4,自引:0,他引:4
In this study, (1) change in the concentration of bisphenol A (BPA) leached from polycarbonate (PC) tube to control water (BPA free), seawater and river water at 20 and 37 degrees C as a function of time, (2) the fate of BPA caused by addition of H(2)O(2) and Fe(3+) to seawater containing BPA leached from PC tube were assessed. BPA leached from PC tube to all water samples increased with the ascendant of temperature and with the passage of time. The BPA leaching velocity in seawater was the fastest in three samples (11 ng/day for seawater, 4.8 ng/day for river water 0.8 ng/day for control water at 37 degrees C).BPA leaching velocity from PC tube was significantly high at pH 8 (50 mM Na(2)HPO(4)) and increased dose-dependently. There was no difference in the velocity of BPA among the 50 mM phosphate-buffers at pH 6.5, 7.0 and 7.5. BPA was leached three times higher by addition of Na(+) than K(+). However, the higher the K(+) concentration, the larger the BPA leached from PC tube. Na(+) mixed with PO(4)(-) was effective on BPA leaching from PC tube, but not with SO(4)(-) or Cl(-). The results suggested that BPA leaching from PC tube would be attributed to the concentration of bibasic phosphate such as Na(2)HPO(4) and K(2)HPO(4) in water samples. BPA was degraded in both control water and seawater in the presence of radical oxygen species, but the degradation rate was lower in seawater than in control water, suggesting that anti-oxidative system exists in seawater. Neo-synthesized substance in both control water and seawater in the presence of reactive oxygen species was identified as BPA-quinone by LC-MS. 相似文献
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Short-term experiments were conducted to investigate the effect of a commercial Fe and an iron-bearing clay mineral, ferruginuous smectite (SWa-1), on the degradation of pentachloroethane (PCA). After 3 h of contact time, SWa-1 catalyzed PCA dehydrochlorination to tetrachloroethene (PCE, 65% conversion), whereas commercial Fe promoted PCA stepwise dechlorination via dehydrochlorination (approximately 40% conversion) and subsequent PCE hydrogenolysis to trichloroethene (TCE). The addition of unaltered SWa-1 to commercial Fe led to a complete inhibition on TCE production, whereas the addition of reduced SWa-1 barely resulted in a 30% decrease. 相似文献
958.
概述了高速微涡活性污泥法的工艺特点,并对该法提高氧的转移及利用效率进行了研究和机理分析。 相似文献
959.
Melissa Fiffer Choong-Min Kang Weeberb J. Requia Petros Koutrakis 《Journal of the Air & Waste Management Association (1995)》2020,70(7):700-707
ABSTRACT
Ultrafine particles (UFPs) pose a human health risk as they can penetrate deep into the respiratory system. The Harvard supersite in Boston, MA provides one of the longest time series of UFP concentrations. This study examined the hypothesis that long-term reductions in PM2.5 mass and sulfur have influenced UFP trends by limiting the ability of UFPs to coagulate onto the accumulation mode via polydisperse coagulation with larger particles. The study used Generalized Additive Models (GAMs) to assess whether changes in PM2.5 mass and sulfur concentrations resulted in smaller than expected (assuming no change in PM2.5 mass or sulfur) decreases in daily UFP trends over the 20-year period from 1999 to 2018. The impact of PM2.5 mass and sulfur changes were represented as UFP penalties. Bootstrapping was applied to calculate standard errors for the different trend and penalty estimates. Results showed that PM2.5 mass and sulfur concentrations declined significantly over the study period. The analysis found an estimated 7.3% (95% CI: 3.5, 11.1%) UFP penalty due to long-term PM2.5 mass trends, and a 9.9% (95% CI: 6.2, 13.7%) UFP penalty due to long-term sulfur trends. Findings from this study suggest that future UFP control efforts should account for the role of PM2.5 mass and sulfur changes. 相似文献
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农林生物质是一种成本低、环境友好的重金属废水处理材料,也是受重金属污染环境的修复材料之一.实验讨论了初始pH值、米糠用量、吸附时间对含铬(Ⅵ)水溶液解毒的影响.结果表明,米糠对Cr(Ⅵ)存在吸附作用,同时也有解毒还原能力.100 mL浓度为100 mg/L的含铬溶液,在初始pH为2、米糠用量为3 g、吸附-反应平衡时间7 h的条件下,生物质吸附去除溶液中的铬为14.4%,而原溶液中Cr(Ⅵ)解毒了57.2%,米糠生物质吸附总铬的能力为0.48 mg Cr/g(生物质).米糠生物质有潜在的吸附铬和修复受铬污染环境的利用价值. 相似文献