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761.
油罐中油气爆炸规律研究   总被引:2,自引:0,他引:2  
建立了油料储罐油气爆炸模拟实验系统,并在模拟实验的基础上,分析了不同因素对爆炸压力的影响及爆炸产物的分布规律.结果表明,油气浓度、罐内初始温度等对油罐油气混合物爆炸过程有重要影响,且存在临界油气浓度(2.5%)及临界初始温度(306 K),在临界值下,油气爆炸最为剧烈.当油气浓度小于临界浓度时,爆炸产物中CO2浓度高于CO浓度,而大于临界浓度时,爆炸产物中CO2浓度小于CO浓度.本研究可为油料储罐油气爆炸灾害事故的防治及安全规程的制定提供参考.  相似文献   
762.
The low-heat-value cornstalk gas produced in the down-flow fixed bed gasifier was tentatively used for methanol synthesis. The cornstalk gas was purified and the technical procedures such as deoxygenation, desulfurization, catalytic cracking of tar, purification and hydrogenation were studied. The catalytic experiments of methanol synthesis with cornstalk syngas were carried out in a tubular-flow integral and isothermal reactor. The effect of reaction temperature, pressure, catalyst types, catalyst particle size, syngas flow at entering end and composition of syngas was investigated. The optimum process conditions and yield of methanol from cornstalk syngas were obtained. The experimental results indicated that the proper catalyst for the synthetic reaction was C301 and the optimum catalyst size was 0.833 mm x 0.351 mm. The optimum operating temperature and pressure were found to be 235癈 and 5 MPa, respectively. The suitable syngas flow 0.9-1.10 mol/h at entering end was selected and the best composition of syngas were CO 10.49%, CO2 8.8%, N2 37.32%, CnHm 0.95% and H2 40.49%. The best methanol yield was 0.418 g/g cornstalk. This study provided the technical support for the industrial test of methanol production from biomass (cornstalk) gas.  相似文献   
763.
中国液态生物质燃料潜力测算为下一步开发提供依据.该文对我国发展液态生物质燃料原料的分布进行整合,从宜能荒地测算、高浓度酒精降度模拟和餐饮地沟油估算等方面,对生产燃料乙醇和生物柴油的原料潜力进行梳理.利用覆盖甜高粱、木薯、甘薯、食用酒精、麻疯树、黄连木和餐饮地沟油等原料来源的数据,测算了我国液态生物质燃料的潜力产量,发现:到2030年,我国燃料乙醇生产潜力将达到5 500万t左右,生物柴油生产潜力将达到3 200万t左右,将能有效保证我国经济增长对能源的需求和缓解化石能源对外依存度过离的能源安全威胁.同时,应该在生物质燃料产业化的关键技术研究上寻求突破,并配套以政府部门的补贴政策,提升我国生物质燃料产业化初期的综合实力.  相似文献   
764.
Recent advances in combustion theories are reviewed, especially the detailed mechanisms of hydrocarbon oxidation, formation of polynuclear aromatic hydrocarbon from aliphatic fuels, and the behavior of halogens in flames. Experimental observations of polychlorinated dibenzo‐p‐dioxins and dibenzofurans (PCDD/F) formation in combustion of aliphatic fuels such as acetylene, ethylene and methane in the presence of hydrogen chloride are summarized. Then, from combustion chemistry considerations a reaction mechanism for T4CDD/F formation in the CH4/ HCl/O2 system is developed. This mechanism consists of elementary reactions describing the main oxidation steps, formation of chlorinated C1‐ to C4‐species, formation of the first aromatic ring, and T4CDD/F formation. The mechanism may be extended to other hydrocarbon fuels and higher PCDD/F homologues. Possible relevance of the mechanism to the “trace chemistries of fire hypothesis”; is discussed.  相似文献   
765.
Twenty four waste cellular phones, manufactured between 2002 and 2011, were selected in order to determine the total heavy metal content in each of their parts (printed circuit boards (PCBs), plastic housing (PH) and liquid crystal display monitors (LCDs)) and compare the results with the permissible limits set by the 2003 Directive on Restriction of Hazardous Substances (RoHS). All the selected samples were pulverized and digested with strong acids. Inductively coupled plasma-mass spectrometry was used to measure the heavy metal content in each sample. The results revealed that concentration levels of the examined heavy metals were higher in PCBs, followed by PH and LCD in that particular order (PCB > PH > LCD). With the exception of Pb and Cr present in PCBs of mobile phones released before the year 2006, all the other metal concentrations were according to the Directive. Concentration levels of Cd, Hg were lower than the permissible limits set by the EU, either before or after the validity of the 2003 RoHS Directive. Considering their significant heavy metal content, coupled with their large quantities produced worldwide in an annual rate, waste cellular phones need to be treated under an environmentally sound management scheme, prioritizing recycling and at the same time eliminating the possibility of any harm.  相似文献   
766.
The Outer Loop landfill bioreactor (OLLB) in Louisville, KY, USA has been the site of a study to evaluate long-term bioreactor performance at a full-scale operational landfill. Three types of landfill units were studied including a conventional landfill (Control cell), a new landfill area that had an air addition and recirculation piping network installed as waste was being placed (As-Built cell), and a conventional landfill that was modified to allow for liquids recirculation (Retrofit cell). During the monitoring period, the Retrofit, Control, and As-Built cells received 48, 14, and 213 L Mg?1 (liters of liquids per metric ton of waste), respectively. The leachate collection system yielded 60, 57 and 198 L Mg?1 from the Retrofit, Control, and As-Built cells, respectively. The head on liner in all cells was below regulatory limits. In the Control and As-Built cells, leachate head on liner decreased once waste placement stopped. The measured moisture content of the waste samples was consistent with that calculated from the estimate of accumulated liquid by the liquid balance. Additionally, measurements on excavated solid waste samples revealed large spatial variability in waste moisture content. The degree of saturation in the Control cells decreased from 85% to 75%. The degree of saturation increased from 82% to 83% due to liquids addition in the Retrofit cells and decreased back to 80% once liquid addition stopped. In the As-Built cells, the degree of saturation increased from 87% to 97% during filling activities and then started to decrease soon after filling activities stopped to reach 92% at the end of the monitoring period. The measured leachate generation rates were used to estimate an in-place saturated hydraulic conductivity of the MSW in the range of 10?8 to 10?7 m s?1 which is lower than previous reports. In the Control and Retrofit cells, the net loss in liquids, 43 and 12 L Mg?1, respectively, was similar to the measured settlement of 15% and 5–8% strain, respectively (Abichou et al., 2013). The increase in net liquid volume in the As-Built cells indicates that the 37% (average) measured settlement strain in these cells cannot be due to consolidation as the waste mass did not lose any moisture but rather suggests that settlement was attributable to lubrication of waste particle contacts, softening of flexible porous materials, and additional biological degradation.  相似文献   
767.
Microbial fuel cells (MFC) utilize microbes as catalysts to convert chemical energy to electricity. Inocula used for MFC operation must therefore contain active microbial population. The dye reduction-based electron-transfer activity monitoring (DREAM) assay was employed to evaluate different inocula used in MFCs for their microbial bioelectrical activity. The assay utilizes the redox property of Methylene Blue to undergo color change from blue to colorless state upon microbial reduction. The extent of Methylene Blue reduction was denoted as the DREAM assay coefficient. DREAM assay was initially performed on a microbial culture along with the growth curve and estimation of colony forming units (CFUs). DREAM coefficient correlated to the CFU/mL obtained over time as growth progressed. The assay was then extended to water samples (domestic sewage, lake and a man-made pond) serving as inocula in MFCs. Domestic wastewater gave the highest DREAM coefficient (0.300 ± 0.05), followed by pond (0.224 ± 0.07) and lake (0.157 ± 0.04) water samples. Power density obtained conformed to the DREAM coefficient values, with the three samples generating power densities of 46.45 ± 5.1, 36.12 ± 3.2 and 25.08 ± 4.3 mW/m2 respectively. We have also studied the role of addition of various carbon sources and their concentrations towards improving the sensitivity of the assay. The DREAM assay is a rapid, easy-to-perform and cost-effective method to assess inocula for their suitability as anolytes in terms of electron transfer potential in MFCs.  相似文献   
768.
Household fuel use in developing countries, particularly as biomass and coal, is a major source of carbonaceous aerosols and other air pollutants affecting health and climate. Using state-of-the-art emission inventories, a global three-dimensional photochemical tracer/transport model of the troposphere, and a global radiative transfer model based on methods presented in the latest IPCC Assessment Report (2007-AR4), we estimate the radiative forcing (RF) attributable to household fuel combustion in Asia in terms of current global annual-mean RF and future global integrated RF for a one-year pulse of emissions (2000) over two time horizons (100 and 20 years). Despite the significant emissions of black carbon (BC) aerosols, these estimates indicate that shorter-lived (non-Kyoto) air pollutants from household fuel use in the region overall seem to exert a small net negative RF because of the strong influence of reflective aerosols. There are, however, major uncertainties in emission estimates for solid fuel burning, and about the sustainability of household fuel wood harvesting in Asia (the carbon neutrality of harvesting). In addition, there is still substantial uncertainty associated with the BC radiative forcing. As a result we find that the sign of the RF from household biomass burning in the region cannot be established. While recognizing the value of integrating climate change and air pollution policies, we are concerned that for a ‘Kyoto style’ post-Kyoto treaty (with global cap-and-trade and the Global Warming Potential as the metric) expanding the basket of components with a selection of short-lived species without also including the wider range of co-emitted species may lead to unintended consequences for global-scale climate. Additional measurement, modelling, and policy research is urgently needed to reduce the uncertainties so that the net impact on climate of emissions and mitigation measures in this sector can be accurately assessed.  相似文献   
769.
模拟了车用工况下燃料电池发动机脉冲式排氢的特点,设计开发了一套质子交换膜燃料电池的尾气净化系统,并以5 kW燃料电池的尾气排放为例,研究其净化效果。研究了电池阳极排放氢气缓冲前后尾气中氢气浓度的变化,以及不同空速条件下氢气的去除效果。结果表明:电堆阳极排放氢气经过缓冲处理后,尾气中氢气浓度趋于平稳,大部分工况下处在2%以下,达到了安全处理的要求;尾气中氢气的去除效果与空速密切相关。对自制的整体式催化剂而言,当空速低于20 000 h-1时,氢气的去除率能达到约95%,而当空速达到39 270 h-1时,氢气的去除率仅为10.9%。鉴于这一问题,提出通过采用尾排空气的分流手段调整催化燃烧反应器对空速的要求,以提高尾气中氢气的去除率。  相似文献   
770.
Sampling and monitoring for cyanotoxins can be problematic as concentrations change with environmental and hydrological conditions. Current sampling practices (e.g. grab samples) provide data on cyanotoxins present only at one point in time and may miss areas or times of highest risk. Recent research has identified the widespread distribution of anatoxin-producing benthic cyanobacteria in rivers highlighting the need for development of effective sampling techniques. In this study we evaluated the potential of an in situ method known as solid phase adsorption toxin tracking (SPATT) for collecting and concentrating anatoxin-a (ATX) and homoanatoxin-a (HTX) in river water. Fifteen different adsorption substrates were screened for efficiency of ATX uptake, nine of which retained high proportions (>70%) of ATX. Four substrates were then selected for a 24-h trial in a SPATT bag format in the laboratory. The greatest decrease in ATX in the water was observed with powdered activated carbon (PAC) and Strata-X (a polymeric resin) SPATT bags. A 3-d field study in a river containing toxic benthic cyanobacterial mats was undertaken using PAC and Strata-X SPATT bags. ATX and HTX were detected in all SPATT bags. Surface grab samples were taken throughout the field study and ATX and HTX were only detected in one of the water samples, highlighting the limitations of this currently used method. Both Strata-X and PAC were found to be effective absorbent substrates. PAC has the advantage that it is cheap and readily available and appears to continue to sorb toxins over longer periods than Strata-X. SPATT has the potential to be integrated into current cyanobacterial monitoring programmes and would be a very useful and economical tool for early warning of ATX and HTX contamination in water.  相似文献   
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