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601.
Yifang Zhu Elinor Fanning Rong Chun Yu Qunfang Zhang John R. Froines 《Atmospheric environment (Oxford, England : 1994)》2011,45(36):6526-6533
Real time number concentrations and size distributions of ultrafine particles (UFPs, diameter <100 nm) and time integrated black carbon, PM2.5 mass, and chemical species were studied at the Los Angeles International Airport (LAX) and a background reference site. At LAX, data were collected at the blast fence (∼140 m from the takeoff position) and five downwind sites up to 600 m from the takeoff runway and upwind of the 405 freeway. Size distributions of UFPs collected at the blast fence site showed very high number concentrations, with the highest numbers found at a particle size of approximately 14 nm. The highest spikes in the time series profile of UFP number concentrations were correlated with individual aircraft takeoff. Measurements indicate a more than 100-fold difference in particle number concentrations between the highest spikes during takeoffs and the lowest concentrations when no takeoff is occurring. Total UFP counts exceeded 107 particles cm−3 during some monitored takeoffs. Time averaged concentrations of PM2.5 mass and two carbonyl compounds, formaldehyde and acrolein, were statistically elevated at the airport site relative to a background reference site. Peaks of 15 nm particles, associated with aircraft takeoffs, that occurred at the blast fence were matched with peaks observed 600 m downwind, with time lags of less than 1 min. The results of this study demonstrate that commercial aircraft at LAX emit large quantities of UFP at the lower end of currently measurable particle size ranges. The observed highly elevated UFP concentrations downwind of LAX associated with aircraft takeoff activities have significant exposure and possible health implications. 相似文献
602.
603.
604.
向膜生物反应器(MBR)中投加ABS颗粒,以干扰膜表面泥饼层的形成和减轻膜污染的发生。结果表明,向MBR中投加粒径为1 mm的ABS颗粒,发现颗粒的最佳投加量为1.5 kg/m3,投加颗粒的膜运行时间是对照实验运行时间的3倍。颗粒对膜表面泥饼沉积层抑制明显,与对照实验泥饼层重量最大相差290 g,颗粒使膜上泥饼层的分布也不同。颗粒的投加也改变了污泥EPS含量,相比对照实验,多糖、蛋白质含量分别提高了17.2%和8%,污泥粘度提高了17.6%。细格栅与颗粒使MBR对TN、TP去除效果分别提高了8.5%和9.7%,对COD的影响不大。 相似文献
605.
Yaacov Mamane Cinzia Perrino Osnat Yossef Maria Catrambone 《Atmospheric environment (Oxford, England : 1994)》2008,42(24):6114-6130
Fine and coarse atmospheric particles were collected in Ashdod—a midsize industrial city on the southeastern Mediterranean coast, and in Gedera—a rural site, to characterize ambient particles and to determine their long-range transport during two major seasons—winter and summer. Manual PM2.5 and PM10 samplers, dichotomous samplers, continuous automated PM10 samplers, and denuders were used to sample particulate and gaseous pollutants.Fine and coarse concentrations in Ashdod were 21.2 and 39.6 μg m−3, and 23.9 and 30.5 μg m−3 in the fall–winter and summer campaigns, respectively. Crustal material, as calcites or dolomites mixed with silicates, dominated the coarse fraction and also the fine fraction on dusty days. In the fall–winter, S, P, and Ni were coupled with minerals. Coarse Ni was associated with crustal material during dust storms, while P originated from shipping and deposition of phosphates in the urban area around.Sulfates dominated the fine fractions in the summer season averaging 12 μg m−3. Multivariate analysis indicated that S was associated with As and Se, V and Ni, both associated with heavy fuel combustion, and Zn and Pb. In winter, those mixed sources were local, but in summer they were part of long-range transport. In the fall–winter, Zn and Pb were strongly associated with Mn, Ga, and Cu—elements emitted from either traffic or metal processing plants.Although the influence of crustal material on both size fractions was significant, most heavy metals were associated with PM2.5. Higher concentrations were linked to a larger number of particles in this fraction, to a larger surface area available for biochemical reaction [Harrison, R., Shi, J., Xi, S., Khan, A., Mark, D., Kinnersley, R., Yin, J., Philos, T., 2000. Measurement of number, mass and size distribution of particles in the atmosphere. Philosophical Transactions of the Royal Society 358, 2567–2579], and finally to a larger concern in regards to health effects. 相似文献
606.
This review summarizes the existing knowledge on the occurrence of tire wear particles in the environment, and their ecotoxicological effects. A meta-analysis on tire components in the environment revealed that tire wear particles are present in all environmental compartments, including air, water, soils/sediments, and biota. The maximum Predicted Environmental Concentrations (PECs) of tire wear particles in surface waters range from 0.03 to 56 mg l−1 and the maximum PECs in sediments range from 0.3 to 155 g kg−1 d.w. The results from our previous long-term studies with Ceriodaphnia dubia and Pseudokirchneriella subcapitata were used to derive Predicted No Effect Concentrations (PNECs). The upper ranges for PEC/PNEC ratios in water and sediment were >1, meaning that tire wear particles present potential risks for aquatic organisms. We suggest that management should be directed towards development and production of more environmentally friendly tires and improved road runoff treatment. 相似文献
607.
A. Bulgakov A. Konoplev J. Smith G. Laptev O. Voitsekhovich 《Journal of environmental radioactivity》2009
During the coming years, a management and remediation strategy for the Chernobyl cooling pond (CP) will be implemented. Remediation options include a controlled reduction in surface water level of the cooling pond and stabilisation of exposed sediments. In terrestrial soils, fuel particles deposited during the Chernobyl accident have now almost completely disintegrated. However, in the CP sediments the majority of 90Sr activity is still in the form of fuel particles. Due to the low dissolved oxygen concentration and high pH, dissolution of fuel particles in the CP sediments is significantly slower than in soils. After the planned cessation of water pumping from the Pripyat River to the Pond, significant areas of sediments will be drained and exposed to the air. This will significantly enhance the dissolution rate and, correspondingly, the mobility and bioavailability of radionuclides will increase with time. The rate of acidification of exposed bottom sediments was predicted on the basis of acidification of similar soils after liming. Using empirical equations relating the fuel particle dissolution rate to soil and sediment pH allowed prediction of fuel particle dissolution and 90Sr mobilisation for different remediation scenarios. It is shown that in exposed sediments, fuel particles will be almost completely dissolved in 15–25 years, while in parts of the cooling pond which remain flooded, fuel particle dissolution will take about a century. 相似文献
608.
Vera I. Slaveykova Konstantin Startchev 《Environmental pollution (Barking, Essex : 1987)》2009,157(12):3445-3450
The influence of pH, ionic strength, presence of humic or alginic acids, extracellular polymeric substances (EPS), or freshwater microalga Chlorella kesslerii on the stability and transformation of carboxyl-PEG-CdSe/ZnS core/shell quantum dots (QDs) in terms of number, hydrodynamic size and fluorescence of individual particles, was studied by fluorescence correlation spectroscopy. Obtained results demonstrated that QDs form stable dispersions at nanomolar concentrations under conditions typical for freshwaters. The presence of 5 or 15 mg C L−1 of humic acid or 50 mg C L−1 EPS did not significantly affect these parameters. In contrast, 5 or 50 mg C L−1 alginate at ionic strength of 10 mM shifted the hydrodynamic radius toward larger values, suggesting a possible capture of QDs by the linear alginate chains. The addition of microalga to the QD dispersions resulted in a slight reduction of the number of QDs and a significant decline in the fluorescence of individual QDs. 相似文献
609.
黄河兰州段水环境中多环芳烃污染初步研究 总被引:5,自引:3,他引:5
2004年11月对黄河兰州段11个采样点的水样、悬浮颗粒物和表层沉积物中的多环芳烃(PAHs)污染作了初步研究。调查结果显示,在此河段中,16种优先控制的PAHs均有检出,总PAHs浓度范围分别为水中,2920~6680ng/L;表层沉积物中,960~2940ng/g(干重);悬浮物中,4145~29090ng/g(干重);其中含量较高的是和芘,且分子量较小的PAHs所占的比例较大。来源分析结果显示,黄河兰州段水环境中PAHs的来源是燃烧源和石油源混合的结果,为混合输入型。用生物学阈值对表层沉积物质量进行评价,黄河兰州段表层沉积物的PAHs污染不算严重,偶尔会产生负面生态效应。 相似文献
610.
银川地区大气颗粒物输送路径及潜在源区分析 总被引:4,自引:0,他引:4
利用Traj Stat软件和全球资料同化系统数据,计算了2014—2016年银川市逐日72 h气流后向轨迹,并采用聚类分析方法,结合银川市同期PM~(10)和PM~(2.5)质量浓度数据,分析了银川年及四季气流轨迹特征及其对银川颗粒物浓度的影响.同时,运用潜在源贡献因子分析法(PSCF)和浓度权重轨迹分析法(CWT),探讨了影响银川颗粒物质量浓度的潜在源区及不同源区对银川颗粒物质量浓度的贡献.结果表明,输送距离最长、高度最高、移速最快的西北气流轨迹占总轨迹的比例最高,达66.7%,且气团移动速度和高度与轨迹距离呈正比;输送高度较低、距离最短、移速最慢的北方气流轨迹占总轨迹数的24.3%;东南气团占总轨迹数的9%,输送距离和移速介于前两者之间,但输送高度较西北气流和北方气流低.四季各类气流轨迹变化特征与年变化特征基本一致,春、秋、冬三季,中、短距离西北气流占气流轨迹总数的比例最高,夏季东南气流占比最高,且夏季南方气流和北方气流占比较春、秋两季高,冬季未出现南方气流和北方气流,春季和冬季气流轨迹输送距离普遍比夏季和秋季长;春、夏、秋三季,偏南气流的输送高度均最低,四季长距离西北气流的输送高度均最高.年及四季都表现为西北气流轨迹对应的银川PM_(10)和PM_(2.5)平均浓度均较高,是影响银川颗粒物质量浓度的最重要输送路径,其次是东南气流轨迹,北方气流轨迹对银川颗粒物浓度影响较小.PSCF和CWT分析发现,位于新疆、甘肃、蒙古国、内蒙古、青海的西北源区及四川、陕西的东南源区是影响银川PM_(10)和PM_(2.5)浓度的两个主要潜在源区,各季节区域范围有所差异. 相似文献