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941.
北京餐饮源排放细粒子理化特征及其对有机颗粒物的贡献 总被引:10,自引:6,他引:4
调研了北京餐饮业发展现状,通过在线监测、采样分析等手段研究北京4家不同烹调方式的餐馆所排放颗粒物的质量浓度、粒径分布、形貌特征、化学组分,并初步估算餐饮源排放细粒子对北京细粒子中颗粒有机物的贡献.结果表明,餐馆的原料、烹饪过程、油烟去除装置以及客流量都会影响餐馆所排放颗粒物的物理、化学性质.样本餐馆营业期间排放颗粒物PM2 .5质量浓度是当日环境大气PM2 .5质量浓度的8~35倍,PM1 .0在PM2 .5的质量浓度中约占50%~85%.餐饮源排放颗粒物多以固态和液态颗粒物形貌存在,化学组分质量百分数由多到少依次是有机物、无机离子和元素碳,分别占到PM2 .5质量浓度的70%左右、5%~11%和小于2%.初步估计结果表明,北京餐饮源排放细粒子对有机颗粒物的贡献和交通源的排放相当,成为北京细粒子有机颗粒物的主要来源之一.认识餐饮源排放颗粒物的理化性质,可以为改善北京空气质量和保证居民身体健康提供数据支持. 相似文献
942.
针对石化工业废水开展沸石强化脱氮处理试验研究,通过比较沸石浓度25mg/L与空白,以及沸石浓度25 mg/L与50mg/L两阶段脱氮效果,探讨沸石促进脱氮功能的机理,结果表明,曝气池中投加沸石可明显提高氨氮和总氮的去除率,硝化细菌总数和硝化功能也得到增强。与空白对照组相比, 沸石浓度25mg/L的试验组运行稳定后,氨氮去除率提高约10%~13%,总氮去除率约提高13%,出水中NO3--N含量约提高100%,氨氮与总氮之比下降6%,内源硝化耗氧呼吸速率可提高138%,硝化细菌总数是空白对照组2.2folds。沸石浓度提高到50mg/L后,试验组的脱氮效果略有增加,但效果不明显。通过对试验结果的关联分析,认为沸石提高系统脱氮能力的原因一方面是因为沸石对NH4+及硝态氮的交换吸附,另一方面NH4+离子富集于沸石表面及内部、沸石颗粒独特的好氧-缺氧微环境,以及沸石离解出CO32- 或HCO3-增加碱度等条件,促进了硝化细菌和反硝化细菌的生长,从而提高了系统脱氮能力。 相似文献
943.
The catalyst of Fe-Mo/ZSM-5 has been found to be more active than Fe-ZSM-5 and Mo/ZSM-5 separately for selective catalytic reduction (SCR) of nitric oxide (NO) with NH3. The kinetics of the SCR reaction in the presence of O2 was studied in this work. The results show that the observed reaction orders were 0.74-0.99, 0.01-0.13, and 0 for NO, O2 and NH3, respectively, at 350-450℃. And the apparent activation energy of the SCR was 65 kJ/mol on the Fe-Mo/ZSM-5 catalyst. The SCR mechanism was also deduced. Adsorbed NO species can react directly with adsorbed ammonia species on the active sites to form N2 and H2O. Gaseous O2 might serve as a reoxidizing agent for the active sites that have undergone reduction in the SCR process. It is also important to note that a certain amount of NO was decomposed directly over the Fe-Mo/ZSM-5 catalyst in the absence of NH3. 相似文献
944.
945.
江西省陆地生态系统氮平衡的时空分布规律研究 总被引:4,自引:1,他引:3
利用系统物质平衡模型,对1995-2005年江西省陆地生态系统的N收支平衡进行了核算,并分析了不同来源N收支量的时间序列特征以及N盈余强度的空间分布特征,探讨了自然灾害和政策实施对N平衡的影响.结果表明:江西省陆地生态系统的N输入量变化范围是(155.5-184.2)×107kg·a-1,平均值为168.5 ×107 ... 相似文献
946.
947.
948.
949.
Some emerging technologies are expected to be pivotal for solving many of the environmental challenges faced today, especially those related to energy. However, many of these technologies may incur significant environmental impacts over their life cycle, while having environmental benefits during their use. This paper presents results of a Life Cycle Assessment (LCA) of a proposed type of nanophotovoltaic, quantum dot photovoltaic (QDPV) module. The LCA is confined to the stages of raw materials acquisition, manufacturing, and use. The impacts of QDPV are compared with other types of PV modules and energy sources - both renewable and nonrenewable. To provide a comprehensive comparative assessment, QDPV modules were compared with mature as well as emerging PV types for which data are available. Comparative assessment with other types of energy sources includes coal, oil, lignite, natural gas, diesel, nuclear, wind, and hydropower.QDPV modules may have the potential to overcome two current barriers of solar technology: low efficiencies and high manufacturing costs. If higher efficiencies are realized, QDPV modules could pave the way to large scale implementation of solar energy, helping nations move toward greater energy independence. On the other hand, candidate materials as quantum dots for solar cell applications are mostly compound semiconductors such as cadmium selenide, cadmium telluride, and lead sulfide which may be toxic and for which renewable options are limited. Toxic effects of these materials may be exacerbated by their nanoscale features.The LCA was carried out using the software SimaPro, and the Ecoinvent Life Cycle Inventory (LCI) database supplemented with available literature and patent information. Our results indicate that while QDPV modules have shorter Energy PayBack Time (EPBT), lower Global Warming Potential (GWP), SOx and NOx emissions than other types of PV modules, they have higher heavy metal emissions, underscoring the need for investigation of emerging technologies, especially nano-based ones, from a life cycle perspective. QDPV modules are better in all impact categories assessed than carbon-based energy sources but they have longer EPBT than wind and hydropower and higher GWP. 相似文献
950.
A little known side effect of the atmospheric air pollution is the degradation of photovoltaic (PV) cells’ performance due to the deposition of solid particles varying in composition, size and origin. In this context, an experimental-based investigation is conducted in order to compare the energy performance of two identical pairs of PV-panels; the first being clean and the second being artificially polluted with ash, i.e. a by-product of incomplete hydrocarbons’ combustion mainly originating from thermal power stations and vehicular exhausts. A series of systematic measurements of current intensity, voltage output and solar radiation are executed simultaneously for the clean and the polluted PV-panel, so that the effect of several mass depositions on the PVs’ power output, energy yield and conversion efficiency may be determined. According to the results, a considerable deterioration of the PV-panels’ performance is obtained, i.e. almost 30% energy reduction per hour or 1.5% efficiency decrease (in absolute terms) for ash accumulation on the panels’ surface reaching up to 0.4 mg/cm2. 相似文献