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971.
湿地资源开发利用及生态功能恢复 总被引:1,自引:0,他引:1
采用生态环境现状调查方法,查清了辽河三角洲资源种类、数量、分布、物种多样性组成、生境条件。分析了生态系统整体性特点、结构、环境服务功能、湿地资源动态变化对生态环境影响。为保护生态功能,提出了有效的恢复性措施。 相似文献
972.
973.
974.
对环境教育与化学实验教学的体系,作了一些有益的探索和尝试,并结合实际工作经验提示了一系列改进实验,减少污染的科学实验方法。 相似文献
975.
976.
介绍了人居环境的定义,并根据全面性、以人为本、可操作性、相对独立性的原则选取评价指标和构建指标体系。采用层次分析法对各指标和子系统赋予不同的权重,利用综合加权求和的方法得出该生态示范区的社会经济,基础设施和公共服务设施,生态环境以及人居环境在1999年和2000年的综合评价指数,对比人居环境1999年和2000年的评价指数,从而得出南充城市人居环境的指数在增大,状况是在不断改善,并从不同的角度给南充城市人居环境建设提出了一些建议,比如:园地制宜,采用多种投资方式加快城市基础设施和公共服务设施建设;优化城市布局,改善能源结构,加大环境治理投资,改善生态环境;加大宣传力度,提高城市可持续管理意识;坚持以人为本,搞好城市人居环境的规划和设计改善措施。 相似文献
977.
978.
Adsorption of phenolic compounds from aqueous solutions by a water-compatible hypercrosslinked polymeric adsorbent 总被引:18,自引:0,他引:18
A water-compatible hypercrosslinked polymeric adsorbent (NJ-8) for adsorbing and removing phenolic compounds from their aqueous solutions was prepared. This product can be used directly without a wetting process. Its adsorption property toward four phenolic compounds, phenol, p-cresol, p-chlorophenol, and p-nitrophenol was tested using the commercial Amberlite XAD-4 as a reference. The capacities of equilibrium adsorption for all four phenolic compounds on the NJ-8 from their aqueous solutions are around two times as high as that of Amberlite XAD4 within the temperature range 283-323 K, which may contribute to their micropore structure and the partial polarity on the network. Freundlich isotherm equations, as well as relative adsorption capacities and isosteric adsorption enthalpies for the four phenolic compounds, indicate that the adsorption of phenolic compounds on the NJ-8 resin is a physical adsorption process. Mini-column adsorption studies for phenol on Amberlite XAD4 and NJ-8 resins show that the breakthrough adsorption capacities are 0.54 and 0.99 mmol/ml, and the total capacities are 0.62 and 1.37 mmol/ml, while no extra acetone was needed to remove the adsorbed phenol from NJ-8 as from Amberlite XAD4. 相似文献
979.
980.
Vertical distribution of polycyclic aromatic hydrocarbons in atmospheric boundary layer of Beijing in winter 总被引:1,自引:0,他引:1
Shu Tao Yi Wang Shiming Wu Shuzheng Liu Han Dou Yanan Liu Chang Lang Fei Hu Baoshan Xing 《Atmospheric environment (Oxford, England : 1994)》2007,41(40):9594-9602
Air samples were collected using active samplers at various heights of 8, 15, 32, 47, 65, 80, 102, 120, 140, 160, 180, 200, 240, 280 and 320 m on a meteorological tower in an urban area of Beijing in two campaigns in winter 2006. Altitudinal distributions of polycyclic aromatic hydrocarbons (PAHs) in atmospheric boundary layer of Beijing in winter season were investigated. Meteorological conditions during the studied period were characterized by online measurements of four meteorological parameters as well as trajectory calculation. The mean total concentrations of 15 PAHs except naphthalene of gaseous and particulate phase were 667±450 and 331±144 ng m−3 in January and 61±19 and 29±6 ng m−3 in March, respectively. Domestic coal combustion and vehicle emission were the dominant PAH sources in winter. Although the composition profiles derived from the two campaigns were similar, the concentrations were different by one order of magnitude. The higher concentrations in January were partly caused by higher emission due to colder weather than March. Moreover, weak wind, passing through the city center before the sampling site, picked up more contaminants on the way and provided unfavorable dispersion condition in January. For both campaigns, PAH concentrations decreased with heights because of ground-level emission and unfavorable dispersion conditions in winter. The concentration ratio of PAHs in gas versus solid phases was temperature dependent and negatively correlated to their octanol–air partition coefficients. 相似文献