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951.
黄土丘陵区不同有机碳背景下侵蚀坡面土壤呼吸特征   总被引:4,自引:1,他引:3  
以黄土丘陵区5个不同有机碳背景的坡面S型小区(坡顶为对照区、坡中为侵蚀区、坡脚为沉积区)为研究对象,通过对土壤呼吸速率的动态观测,分析坡面不同类型区土壤呼吸特征及其与土壤温湿度、有机碳和坡位的关系.结果表明,土壤温度的变化对沉积区土壤呼吸影响较大,土壤湿度的变化对侵蚀区土壤呼吸影响较大.有机碳是影响土壤呼吸的首要因子,可解释土壤呼吸变异的54.72%;其次是土壤湿度、坡位和土壤温度,分别可解释土壤呼吸变异的18.86%、16.13%和10.29%.侵蚀对坡面土壤呼吸的影响具有明显的原位和异位效应,侵蚀导致坡面侵蚀区土壤呼吸减小了21.14%,沉积区土壤呼吸增大了21.93%.侵蚀坡面土壤碳排放的源汇效应与有机碳水平有关,当土壤有机碳含量大于6.82 g·kg-1时,坡面侵蚀趋向于碳汇过程;当有机碳含量小于3.03 g·kg-1时,坡面侵蚀趋向于碳源过程.文中模型可以较好地反映有机碳和土壤温湿度与土壤呼吸的关系.  相似文献   
952.
953.
温度对厨余垃圾两相厌氧消化中水解和酸化过程的影响   总被引:16,自引:0,他引:16  
赵杰红  张波  蔡伟民 《环境科学》2006,27(8):1682-1686
实验考查了厨余垃圾在4个温度(25℃、37℃、40℃、50℃)条件下的水解率、挥发酸(VFA)产量和速率、乳酸产量和有机酸的组成.结果表明:温度对水解和酸化过程均有较大影响,在小于37℃范围内水解率和酸化率均随温度升高而增加,最大的VFA浓度在37℃下获得,达34.4g/L.超过37℃,酸化率下降而水解率继续增加,最大水解率在50℃下获得达82%.VFA中以甲酸和乙酸为主,并有少量丙酸和丁酸产生,同时乳酸浓度一直较高.通过实验确定了厨余垃圾水解酸化过程的最优温度条件为37℃.  相似文献   
954.
In fractured rocks with a porous rock matrix such as granites, radionuclides will flow with the water in the fracture network. The nuclides will diffuse in and out the rock matrix where they can sorb and be considerably retarded compared to the water velocity. A water parcel entering the network will mix and split at the fracture intersections and parts of the original parcel will traverse a multitude of different fractures. The flowrates, velocities, sizes and apertures of the fractures can vary widely. Normally one must solve the transport equations for every fracture and use the effluent concentration as inlet condition to the next fracture and so on. It is shown that under some weakly simplified conditions it suffices to determine one single parameter group containing information on the flow wetted surface that a water parcel contacts along the entire path. It is also shown how this can be obtained. Then, solving the transport equations only once for time and location along the path gives the concentration and nuclide flux of every nuclide in the chain everywhere along a path. The same solution actually is valid for every path in the network. This dramatically reduces the computation effort. The same approach can be used for models based on streamtubes.  相似文献   
955.
Background, Aims and Scope Polycyclic Aromatic Hydrocarbons (PAHs) are known for their adverse and cumulative effects at low concentration. In particular, the PAHs accumulate in sewage sludge during wastewater treatment, and may thereafter contaminate agricultural soils by spreading sludge on land. Therefore, sludge treatment processes constitute the unique opportunity of PAH removal before their release in the environment. In this study, the ability of aerobic microorganisms to degrade light and heavy PAHs was investigated in continuous bioreactors treating trace-level PAH-contaminated sludge. Methods Several aerobic reactors were operated under continuous and perfectly mixed conditions to simulate actual aerobic sludge digesters. Three sterile control reactors were performed at 35°C, 45°C or 55°C to assess PAH abiotic losses under mesophilic and thermophilic conditions. Three biological reactors were also operated at 35°C, 45°C or 55°C. Furthermore, 250 mM methanol were added in an additional mesophilic reactor (35°C). All reactors were fed with long-term PAH-contaminated sewage sludge, and PAH removal was assessed by inlet/outlet mass balance. In this study, PAH compounds ranged from 2 to 5-unsubstituted aromatic rings, i.e. respectively from Fluorene to Indeno(123cd)pyrene. Results and Discussion Significant abiotic losses were observed for the lightest PAHs (fluorene, phenanthrene and anthracene), while biodegradation occurred for all PAHs. More than 80% of the lightest PAHs were removed. Biodegradation rates inversely correlated with the increasing molecular weight, and seemed limited by the low bioavailability of the heaviest PAHs (only 50% of removal). The enhancement of PAH bioavailability by increasing the process temperature or adding methanol was tested. A temperature increase from 35°C to 45°C and then to 55°C significantly enhanced the biodegradation of the heaviest PAHs from 50% to 80%. However, high abiotic losses were observed for all PAHs at 55°C, which was attributed to volatilization. Optimal conditions were found at 45°C considering the low abiotic losses and the high PAH biodegradation rates. Similar performances were achieved by addition of methanol in the sludge. It was concluded that increasing temperatures or addition of methanol favored PAH diffusion from solids to an aqueous compartment, and enhanced their bioavailability to PAH-degrading microorganisms. Conclusion In this study, the use of long-term acclimated aerobic ecosystems showed the high potential of aerobic microorganisms to degrade a wide range of PAHs at trace levels. However, PAH biodegradation was likely controlled by their low bioavailability. Two aerobic processes have been finally proposed to achieve efficient decontamination of sewage sludge, at 45°C or in the presence of methanol. The PAH concentrations in reactor outlet were lower than the French requirements, and allow the treated sludge to be spread on agricultural land. Recommendations and Outlook The two proposed aerobic processes used physical or chemical diffusing agents. The global ecological impact of using the latter agents for treating trace level contamination must be considered. Since methanol was completely removed during the process, no additional harm is expected after treatment. However, an increase of temperature to 45°C could drastically increase the energy demand in full-scale plants, and therefore the ecological impact of the process. Moreover, since bioavailability controls PAH biodegradation, efficiency of the processes could also be influenced by the hydraulic parameters, such as mixing and aeration rates. Further experimentations in a pilot scale are therefore recommended, as well as a final assessment of the global environmental benefit of using such aerobic processes in the bioremediation of trace level compounds. - Abbreviations (PAHs): Ant – anthracene; B(a)A – benzo(a)anthracene ; B(b)F – benzo(b)fluoranthene; B(k)F – benzo(k)fluoranthene; B(ghi)P – benzo(g,h,i)perylene; B(a)P – benzo(a)pyrene; Chrys – chrysene; DB – dibenzo(a,h)anthracene; Fluor – fluoranthene; Fluo - fluorene; Ind – indeno(1,2,3-c,d)pyrene; Phe - phenanthrene; Pyr – pyrene - * The basis of this peer-reviewed paper is a presentation at the 9th FECS Conference on 'Chemistry and Environment', 29 August to 1 September 2004, Bordeaux, France.  相似文献   
956.
Nanotechnology is a major innovative scientific and economic growth area, which may present a variety of hazards for environmental and human health. The surface properties and very small size of nanoparticles and nanotubes provide surfaces that may bind and transport toxic chemical pollutants, as well as possibly being toxic in their own right by generating reactive radicals. There is a wealth of evidence for the harmful effects of nanoscale combustion-derived particulates (ultrafines), which when inhaled can cause a number of pulmonary pathologies in mammals and humans. However, release of manufactured nanoparticles into the aquatic environment is largely an unknown. This review addresses the possible hazards associated with nanomaterials and harmful effects that may result from exposure of aquatic animals to nanoparticles. Possible nanoparticle association with naturally occurring colloids and particles is considered together with how this could affect their bioavailability and uptake into cells and organisms. Uptake by endocytotic routes are identified as probable major mechanisms of entry into cells; potentially leading to various types of toxic cell injury. The higher level consequences for damage to animal health, ecological risk and possible food chain risks for humans are also considered based on known behaviours and toxicities for inhaled and ingested nanoparticles in the terrestrial environment. It is concluded that a precautionary approach is required with individual evaluation of new nanomaterials for risk to the health of the environment. Although current toxicity testing protocols should be generally applicable to identify harmful effects associated with nanoparticles, research into new methods is required to address the special properties of nanomaterials.  相似文献   
957.
硫高温腐蚀及腐蚀产物氧化自燃性的研究   总被引:1,自引:0,他引:1  
随着炼制原油硫含量的增加,炼油装置的硫腐蚀问题也日益严重.针对硫高温腐蚀状况,用差热-热重分析仪研究硫与Fe(OH)3、Fe2O3和Fe3O4发生硫化腐蚀反应的初始温度,并采用X射线衍射仪鉴定了360 ℃高温无氧条件下硫化腐蚀产物的组成.结果表明,硫与Fe(OH)3、Fe2O3和Fe3O4发生硫化反应的初始温度分别为287.67 ℃、233.34℃和308.47 ℃;高温硫化腐蚀产物主要是FeS2.对硫化产物FeS2进行氧化反应,氧化升温曲线和耗氧曲线表明,硫化腐蚀产物FeS2具有很高的氧化自燃性,在一定条件下能引发油品火灾和爆炸等事故.  相似文献   
958.
钢筋混凝土结构抗火研究进展与趋势   总被引:2,自引:0,他引:2  
李耀庄  唐毓  曾志长 《灾害学》2008,23(1):102-107
火灾高温对钢筋混凝土结构材性有显著影响,极易造成结构损伤、破坏甚至倒塌。在大量阅读国内外文献的基础上,从建筑火灾发展过程研究、钢筋混凝土结构在火灾中的行为研究、钢筋混凝土结构抗火设计方法的研究、火灾后钢筋混凝土结构的损伤评估和加固方法的研究等4个方面对钢筋混凝土结构抗火研究进行了论述;总结了目前国内外钢筋混凝土结构抗火研究的主要进展及成果;指出了结构抗火研究尚存在的一些问题;最后,对结构抗火研究趋势进行了展望。  相似文献   
959.
The paper presents the application of thermal remote sensing for mapping hydrocarbon polluted sites. This has been achieved by mono-window algorithm for land surface temperature (LST) measurements, using multi-date band 6 data of Landsat Thematic Mapper (TM). The emissivity, transmittance and mean atmospheric temperature were used as critical factors to estimate LST. The changes in the surface emissivity due to oil pollution alter the apparent temperature, which was used as a recognition element to map out oil polluted surfaces. The LST contrast was successfully used to map spatial distribution of hydrocarbon pollution in the Burgan Oil field area of Kuwait. The methodology can be positively used to detect waste dumping, oil spills in oceans and ports, besides environmental management of oil pollution at or near the land surface.  相似文献   
960.
陈静  陈敏  王宇  王静 《环境技术》2009,27(6):36-39
本项目结合湖北省科技计划自然科学基金项目“混凝土结构使役环境的智能模拟”,在WTST-150试验机硬件平台基础上,以LabVIEW8.5为开发平台,设计了一套混凝土结构使役环境中温度智能模拟LabVIEW软件,主要包括能初始化程序、温度采集与显示子程序、温度PID控制子程序、温度存储和查询子程序。经投入实验验证,该软件能实现实时曲线显示、温度控制、试验状态和保存试验数据、数据查询、手动加热、分配温度通道、PID控制参数整定、制冷、读入温度曲线等功能。具有实时在线循环检测、采集数据、响应快速等优点,并具有良好的故障诊断能力和可维护性以及超强的纠错能力。本软件完善了WTST-150试验机的温度控制系统,使其更加符合实际工况。  相似文献   
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