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51.
分析了我国居住建筑室内PM_(2.5)污染水平,总结了现阶段PM_(2.5)的研究方法,主要包括理论分析法、数值模拟法和实验测试法。指出室外源是室内PM_(2.5)的主要污染来源,而室内烟草烟雾、烹饪及人员活动也会严重影响室内PM_(2.5)浓度。针对目前研究中存在的问题,提出了标定典型建筑在不同影响因素下的I/O比范围、研究家具和家电的颗粒物释放状况、加强农村室内外空气颗粒物污染调查等建议。 相似文献
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Racha Dejchanchaiwong Napawan Mahasakpan Phatsarakorn Chaisongkaew Muanfun Iner Nobchonnee Nim Worradorn Phairuang Surajit Tekasakul Masami Furuuchi Mitsuhiko Hat Thaniya Kaosol Perapong Tekasakul 《环境科学学报(英文版)》2023,35(2):253-267
Distribution of PM0.1,PM1and PM2.5particle-and gas-polycyclic aromatic hydrocarbons(PAHs) during the 2019 normal,partial and strong haze periods at a background location in southern Thailand were investigated to understand the behaviors and carcinogenic risks PM1was the predominant component,during partial and strong haze periods,accounting for 45.1%and 52.9%of total suspended particulate matter,respectively,while during nor mal period the contribution... 相似文献
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《环境科学学报(英文版)》2023,35(4):708-721
Nowadays, the fine particle pollution is still severe in some megacities of China, especially in the Sichuan Basin, southwestern China. In order to understand the causes, sources, and impacts of fine particles, we collected PM2.5 samples and analyzed their chemical composition in typical months from July 2018 to May 2019 at an urban and a suburban (background) site of Chengdu, a megacity in this region. The daily average concentrations of PM2.5 ranged from 5.6-102.3 µg/m3 and 4.3-110.4 µg/m3 at each site. Secondary inorganics and organic matters were the major components in PM2.5 at both sites. The proportion of nitrate in PM2.5 has exceeded sulfate and become the primary inorganic component. SO2 was easier to transform into sulfate in urban areas because of Mn-catalytic heterogeneous reactions. In contrast, NO2 was easily converted in suburbs with high aerosol water content. Furthermore, organic carbon in urban was much greater than that in rural, other than elemental carbon. Element Cr and As were the key cancer risk drivers. The main sources of PM2.5 in urban and suburban areas were all secondary aerosols (42.9%, 32.1%), combustion (16.0%, 25.2%) and vehicle emission (15.2%, 19.2%). From clean period to pollution period, the contributions from combustion and secondary aerosols increased markedly. In addition to tightening vehicle controls, urban areas need to restrict emissions from steel smelters, and suburbs need to minimize coal and biomass combustion in autumn and winter. 相似文献
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对2005年7月至2006年2月采集到的南京市气溶胶Pm2.5 进行季节性初步分析,并对其中的15种优控多环芳烃(PAHs)进行分析研究,通过比值法判断南京市PAHs夏季主要来源于柴油型燃烧,冬季主要来源于柴油和煤型相结合的燃烧.对15种优控PAHs两两之间的相关性分析,发现各化合物之间显著相关,表明各化合物的来源有相似之处. 相似文献
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PM2.5 (particles with aerodynamic diameters less than 2.5 μm) chemical source profiles applicable to speciated emissions inventories and receptor model source apportionment are reported for geological material, motor vehicle exhaust, residential coal (RCC) and wood combustion (RWC), forest fires, geothermal hot springs; and coal-fired power generation units from northwestern Colorado during 1995. Fuels and combustion conditions are similar to those of other communities of the inland western US. Coal-fired power station profiles differed substantially between different units using similar coals, with the major difference being lack of selenium in emissions from the only unit that was equipped with a dry limestone sulfur dioxide (SO2) scrubber. SO2 abundances relative to fine particle mass emissions in power plant emissions were seven to nine times higher than hydrogen sulfide (H2S) abundances from geothermal springs, and one to two orders of magnitude higher than SO2 abundances in RCC emissions, implying that the SO2 abundance is an important marker for primary particle contributions of non-aged coal-fired power station contributions. The sum of organic and elemental carbon ranged from 1% to 10% of fine particle mass in coal-fired power plant emissions, from 5% to 10% in geological material, >50% in forest fire emissions, >60% in RWC emissions, and >95% in RCC and vehicle exhaust emissions. Water-soluble potassium (K+) was most abundant in vegetative burning profiles. K+/K ratios ranged from 0.1 in geological material profiles to 0.9 in vegetative burning emissions, confirming previous observations that soluble potassium is a good marker for vegetative burning. 相似文献
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Polycyclic aromatic hydrocarbons, black carbon, and molecular markers in soils of Switzerland 总被引:16,自引:0,他引:16
Polycyclic aromatic hydrocarbons (PAH) were analysed in 23 soil samples (0–10 cm layer) from the Swiss soil monitoring network (NABO) together with total organic carbon (TOC) and black carbon (BC) concentration, as well as some PAH source diagnostic ratios and molecular markers. The concentrations of the sum of 16 EPA priority PAHs ranged from 50 to 619 μg/kg dw. Concentrations increased from arable, permanent and pasture grassland, forest, to urban soils and were 21–89% lower than median numbers reported in the literature for similar Swiss and European soils. NABO soils contained BC in concentrations from 0.4 to 1.8 mg/g dw, except for two sites with markedly higher levels. These numbers corresponded to 1–6% of TOC and were comparable to the limited published BC data in soil and sediments obtained with comparable analytical methods. The various PAH ratios and molecular markers pointed to a domination of pyrogenically formed PAHs in Swiss soils. In concert, the gathered data suggest the following major findings: (1) gas phase PAHs (naphthalene to fluorene) were long-range transported, cold-condensated at higher altitudes, and approaching equilibrium with soil organic matter (OM); (2) (partially) particle-bound PAHs (phenanthrene to benzo[ghi]perylene) were mostly deposited regionally in urban areas, and not equilibrated with soil OM; (3) Diesel combustion appeared to be a major emission source of PAH and BC in urban areas; and (4) wood combustion might have contributed significantly to PAH burdens in some soils of remote/alpine (forest) sites. 相似文献
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Municipal wastewater reclamation is becoming of increasing importance in the world to solve the problem of water scarcity. A better understanding of the molecular composition of effluent organic matter(Ef OM) in the treated effluents of municipal wastewater treatment plants(WWTPs) is crucial for ensuring the safety of water reuse. In this study, the molecular composition of Ef OM in the secondary effluent of a WWTP in Beijing and the reclaimed water further treated with a coagulation–sedimentation–ozonation process were characterized using a non-target Fourier transform ion cyclotron resonance mass spectrometry(FT-ICR MS) method and compared to that of natural organic matter(NOM) in the local source water from a reservoir. It was found that the molecular composition of Ef OM in the secondary effluent and reclaimed water was dominated by CHOS formulas, while NOM in the source water was dominated by CHO formulas. The CHO formulas of the three samples had similar origins. Anthropogenic surfactants were responsible for the CHOS formulas in Ef OM of the secondary effluent and were not well removed by the coagulation-sedimentation-ozonation treatment process adopted. 相似文献