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71.
准好氧填埋渗滤液中氮转化机理 总被引:1,自引:0,他引:1
依据准好氧填埋的原理构建了填埋试验装置,在填埋装置各个层次设计采样装置.定期采集渗滤液进行分析,测定各个层次区域渗滤液中氨氮、硝态氮、亚硝态氮和总氮的质量浓度,分析各形态氮之间的变化规律与相关性,初步探讨氮转化的机理.结果表明,准好氧填埋上层区域中,渗滤液的氨氮与硝态氮质量浓度变化相关性极显著;中层和下层区域由于处于兼氧和厌氧状态,硝化作用较弱,渗滤液中氨氮与硝态氮质量浓度变化相关性不显著.上层渗滤液中氨氮与总氮相关性不显著,中层和下层氨氮与总氮相关性极显著,表明中层和下层区域中,渗滤液的氨氮质量浓度变化是导致总氮含量变化的主要贡献因素. 相似文献
72.
Landfill leachate treatment methods: A review 总被引:19,自引:0,他引:19
J. Wiszniowski D. Robert J. Surmacz-Gorska K. Miksch J. V. Weber 《Environmental Chemistry Letters》2006,4(1):51-61
Landfilling of municipal waste is still a major issue of the waste management system in Europe. The generated leachate must
be appropriately treated before being discharged into the environment. Technologies meant for leachate treatment can be classified
as follows (i) biological methods, (ii) chemical and physical methods. Here we review briefly the main processes currently
used for the landfill leachates treatments. 相似文献
73.
不同渗滤液循环方式对填埋层甲烷产生的影响 总被引:16,自引:5,他引:16
通过填埋模拟柱 ,实验室研究了以我国大城市生活垃圾组成为依据的新鲜垃圾填埋层在不同渗滤液循环方式条件下甲烷产生的规律 .渗滤液循环方式包括 :原液循环、好氧预处理 (SBR)后循环、与陈垃圾出水混合后循环 .结果表明 :新鲜垃圾填埋层初期渗滤液COD、VFA浓度高 ,原液循环导致有机酸的积累 ,抑制了甲烷化进程 ;初期渗滤液经预处理控制一定COD、VFA浓度后循环 ,能够显著地缩短产甲烷滞后时间、加速甲烷化进程 ;当填埋层进入稳定的甲烷化阶段后 ,渗滤液循环才能有效地降解渗滤液中的有机污染 ,近 10 0 %地转化为填埋气体. 相似文献
74.
通过DNA提取,PCR扩增和DGGE分离,用BLAST程序进行相似性比较分析体系中微生物群落多样性。所有序列与数据库中16S rDNA序列的相似性在94%~100%之间。从整个挂膜过程考虑,挂膜时间应在8天左右。渗滤液中污染物的去除与投加EM有很大的关系,但是渗滤液中原始菌种的贡献同样不可忽视。投加EM菌剂促进了渗滤液中群落结构演替和功能优化,并最终通过EM菌剂和渗滤液中原始菌群的共同作用实现渗滤液处理系统效能提高和完善。 相似文献
75.
垃圾渗滤液中有机物分子量的分布及在MBR系统中的变化 总被引:33,自引:0,他引:33
利用凝胶层析方法分析了垃圾渗滤液中有机物分子量的分布情况,并考察了利用膜生物反应器(MBR)处理垃圾渗滤液系统中有机污染物分子量的分布以及水溶性腐殖质(AHS)含量的变化.研究发现,垃圾渗滤液中的有机物主要由两部分组成,即分子量大于6000的大分子物质和分子量小于1500的小分子物质.大分子物质主要是水溶性腐殖质,而小分子物质主要由挥发性有机酸及水溶性腐殖质组成.大分子的AHS难以被微生物降解,但能被微滤膜截留.大部分小分子的AHS既难以被微生物降解,又不能被膜截留,是构成MBR处理出水COD的主要成分. 相似文献
76.
77.
Michelle M. Lorah Isabelle M. Cozzarelli J.K. Bhlke 《Journal of contaminant hydrology》2009,105(3-4):99-117
The biogeochemistry at the interface between sediments in a seasonally ponded wetland (slough) and an alluvial aquifer contaminated with landfill leachate was investigated to evaluate factors that can effect natural attenuation of landfill leachate contaminants in areas of groundwater/surface-water interaction. The biogeochemistry at the wetland-alluvial aquifer interface differed greatly between dry and wet conditions. During dry conditions (low water table), vertically upward discharge was focused at the center of the slough from the fringe of a landfill-derived ammonium plume in the underlying aquifer, resulting in transport of relatively low concentrations of ammonium to the slough sediments with dilution and dispersion as the primary attenuation mechanism. In contrast, during wet conditions (high water table), leachate-contaminated groundwater discharged upward near the upgradient slough bank, where ammonium concentrations in the aquifer where high. Relatively high concentrations of ammonium and other leachate constituents also were transported laterally through the slough porewater to the downgradient bank in wet conditions. Concentrations of the leachate-associated constituents chloride, ammonium, non-volatile dissolved organic carbon, alkalinity, and ferrous iron more than doubled in the slough porewater on the upgradient bank during wet conditions. Chloride, non-volatile dissolved organic carbon (DOC), and bicarbonate acted conservatively during lateral transport in the aquifer and slough porewater, whereas ammonium and potassium were strongly attenuated. Nitrogen isotope variations in ammonium and the distribution of ammonium compared to other cations indicated that sorption was the primary attenuation mechanism for ammonium during lateral transport in the aquifer and the slough porewater. Ammonium attenuation was less efficient, however, in the slough porewater than in the aquifer and possibly occurred by a different sorption mechanism. A stoichiometrically balanced increase in magnesium concentration with decreasing ammonium and potassium concentrations indicated that cation exchange was the sorption mechanism in the slough porewater. Only a partial mass balance could be determined for cations exchanged for ammonium and potassium in the aquifer, indicating that some irreversible sorption may be occurring.Although wetlands commonly are expected to decrease fluxes of contaminants in riparian environments, enhanced attenuation of the leachate contaminants in the slough sediment porewater compared to the aquifer was not observed in this study. The lack of enhanced attenuation can be attributed to the fact that the anoxic plume, comprised largely of recalcitrant DOC and reduced inorganic constituents, interacted with anoxic slough sediments and porewaters, rather than encountering a change in redox conditions that could cause transformation reactions. Nevertheless, the attenuation processes in the narrow zone of groundwater/surface-water interaction were effective in reducing ammonium concentrations by a factor of about 3 during lateral transport across the slough and by a factor of 2 to 10 before release to the surface water. Slough porewater geochemistry also indicated that the slough could be a source of sulfate in dry conditions, potentially providing a terminal electron acceptor for natural attenuation of organic compounds in the leachate plume. 相似文献
78.
对城市生活垃圾的分类回收、处理进行了探讨,对完善城市基础设施建设,改善投资环境将起到重要作用。 相似文献
79.
80.
The inorganic nitrogen transformations occurring at a municipal waste leachate treatment facility were investigated. The treatment
facility consisted of a collection well and an artificial wetland between two aeration ponds. The first aeration pond showed
a decrease in ammonium (from 3480 (± 120) to 630(± 90) mg ⋅ L−1), a reduction in inorganic nitrogen load (3480 to 1680 mg N ⋅ L−1), and an accumulation of nitrite (< 1.3 mg-N ⋅ L−1 in the collection well, to 1030 mg-N ⋅ L−1). Incomplete ammonium oxidation was presumably the result of the low concentration of carbonate alkalinity (∼2 mg ⋅ L−1), which may cause a limitation in the ammonium oxidation rate of nitrifiers. Low carbonate alkalinity levels may have been
the result of stripping of CO2 from the first aeration pond at the high aeration rates and low pH. Various chemodenitrification mechanisms are discussed
as the reason for the reduction in the inorganic nitrogen load, including; the reduction of nitrite by iron (II) (producing
various forms of gaseous nitrogen); and reactions involving nitrous acid. It is suggested that the accumulation of nitrite
may be the result of inhibition of nitrite oxidizers by nitrous acid and low temperatures. Relative to the first aeration
pond, the speciation and concentration of inorganic nitrogen was stable in the wetlands and 2nd aeration pond. The limited
denitrification in the wetlands most probably occurred due to low concentrations of organic carbon, and short retention times. 相似文献