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991.
992.
碳羟基磷灰石对水中Cr(Ⅵ)的吸附性能研究 总被引:2,自引:0,他引:2
利用废弃蛋壳为原材料,水热法合成碳羟基磷灰石(CHAP),并利用X射线衍射、扫描电镜、能谱分析手段对其结构进行了表征.将CHAP作为含铬废水的吸附剂,考察了pH、Cr(Ⅵ)初始浓度、吸附时间等对Cr(Ⅵ)吸附行为的影响.结果表明,初始质量浓度为50 mg/L的Cr(Ⅵ)溶液,在常温(22±2) ℃、溶液pH为3.0、CHAP用量为5 g/L时,30 min基本达到吸附平衡,Cr(Ⅵ)去除率为98.3%,饱和吸附容量达29.85 mg/g.CHAP对Cr(Ⅵ)的吸附行为符合Langmuir吸附等温式和Freundlich吸附等温式,相关系数分别为0.998 4和0.922 6.通过10%(体积分数)H2SO4对吸附Cr(Ⅵ)的CHAP进行再生,再生率最高达95.8%. 相似文献
993.
994.
嘉兴市构建的县域跨界水污染补偿机制,不仅是一项流域水污染防治制度刨新,而且是浙江省跨行政区水污染补偿政策的重要支撑和有力保障.通过对大量数据的统计分析,提出了3种补偿标准,并运用跨界水污染补偿模型,模拟测算了2个市级断面和2个县级断面的补偿额.模拟测算结果不但能描绘出县域跨界水污染的现状,而且能够明确补偿对象和补偿额,对流域水质根本改善具有重要意义. 相似文献
995.
由美国次贷危机引发的金融危机已对全球经济产生巨大冲击,也将给世界环境保护工作带来负面效应.客观分析了此次金融危机对中国环境保护带来的挑战和契机,明确指出应充分利用这次契机,除依靠国家宏观经济政策的扶持外,还要通过产业内部调整和完善来积极应对.大力促进中国环境保护事业的新发展. 相似文献
996.
L.J. Deacon L.J. Pankhurst G.H. Drew E.T. Hayes S. Jackson P.J. Longhurst J.W.S. Longhurst J. Liu S.J.T. Pollard S.F. Tyrrel 《Atmospheric environment (Oxford, England : 1994)》2009,43(35):5698-5701
Information on the particle size distribution of bioaerosols emitted from open air composting operations is valuable in evaluating potential health impacts and is a requirement for improved dispersion simulation modelling. The membrane filter method was used to study the particle size distribution of Aspergillus fumigatus spores in air 50 m downwind of a green waste compost screening operation at a commercial facility. The highest concentrations (approximately 8 × 104 CFU m−3) of culturable spores were found on filters with pore diameters in the range 1–2 μm which suggests that the majority of spores are emitted as single cells. The findings were compared to published data collected using an Andersen sampler. Results were significantly correlated (p < 0.01) indicating that the two methods are directly comparable across all particles sizes for Aspergillus spores. 相似文献
997.
Zhi-Ping Wang Yang Song Jay Gulledge Qiang Yu Hong-Sheng Liu Xing-Guo Han 《Atmospheric environment (Oxford, England : 1994)》2009,43(13):2148-2153
A budget for the methane (CH4) cycle in the Xilin River basin of Inner Mongolia is presented. The annual CH4 budget in this region depends primarily on the sum of atmospheric CH4 uptake by upland soils, emission from small wetlands, and emission from grazing ruminants (sheep, goats, and cattle). Flux rates for these processes were averaged over multiple years with differing summer rainfall. Although uplands constitute the vast majority of land area, they consume much less CH4 per unit area than is emitted by wetlands and ruminants. Atmospheric CH4 uptake by upland soils was ?3.3 and ?4.8 kg CH4 ha?1 y?1 in grazed and ungrazed areas, respectively. Average CH4 emission was 791.0 kg CH4 ha?1 y?1 from wetlands and 8.6 kg CH4 ha?1 y?1 from ruminants. The basin area-weighted average of all three processes was 6.8 kg CH4 ha?1 y?1, indicating that ruminant production has converted this basin to a net source of atmospheric CH4. The total CH4 emission from the Xilin River basin was 7.29 Gg CH4 y?1. The current grazing intensity is about eightfold higher than that which would result in a net zero CH4 flux. Since grazing intensity has increased throughout western China, it is likely that ruminant production has converted China's grazed temperate grasslands to a net source of atmospheric CH4 overall. 相似文献
998.
Ionic composition of TSP and PM2.5 during dust storms and air pollution episodes at Xi'an,China 总被引:1,自引:0,他引:1
Zhenxing Shen Junji Cao Richard Arimoto Zhiwei Han Renjian Zhang Yuemei Han Suixin Liu Tomoaki Okuda Shunsuke Nakao Shigeru Tanaka 《Atmospheric environment (Oxford, England : 1994)》2009,43(18):2911-2918
TSP and PM2.5 samples were collected at Xi'an, China during dust storms (DSs) and several types of pollution events, including haze, biomass burning, and firework displays. Aerosol mass concentrations were up to 2 times higher during the particulate matter (PM) events than on normal days (NDs), and all types of PM led to decreased visibility. Water-soluble ions (Na+, NH4+, K+, Mg2+, Ca2+, F?, Cl?, NO3?, and SO42?). were major aerosol components during the pollution episodes, but their concentrations were lower during DSs. NH4+, K+, F?, Cl?, NO3?, and SO42? were more abundant in PM2.5 than TSP but the opposite was true for Mg2+ and Ca2+. PM collected on hazy days was enriched with secondary species (NH4+, NO3?, and SO42) while PM from straw combustion showed high K+ and Cl?. Firework displays caused increases in K+ and also enrichments of NO3? relative to SO42?. During DSs, the concentrations of secondary aerosol components were low, but Ca2+ was abundant. Ion balance calculations indicate that PM from haze and straw combustion was acidic while the DSs samples were alkaline and the fireworks' PM was close to neutral. Ion ratios (SO42?/K+, NO3?/SO42?, and Cl?/K+) proved effective as indicators for different pollution episodes. 相似文献
999.
Junfeng Liu Denise L. Mauzerall Larry W. Horowitz 《Atmospheric environment (Oxford, England : 1994)》2009,43(28):4339-4347
In this second of two companion papers, we quantify for the first time the global impact on premature mortality of the inter-continental transport of fine aerosols (including sulfate, black carbon, organic carbon, and mineral dust) using the global modeling results of (Liu et al., 2009). Our objective is to estimate the number of premature mortalities in each of ten selected continental regions resulting from fine aerosols transported from foreign regions in approximately year 2000. Our simulated annual mean population-weighted (P-W) concentrations of total PM2.5 (aerosols with diameter less than 2.5 μm) are highest in East Asia (EA, 30 μg m?3) and lowest in Australia (3.6 μg m?3). Dust is the dominant component of PM2.5 transported between continents. We estimate global annual premature mortalities (for adults age 30 and up) due to inter-continental transport of PM2.5 to be nearly 380 thousand (K) in 2000. Approximately half of these deaths occur in the Indian subcontinent (IN), mostly due to aerosols transported from Africa and the Middle East (ME). Approximately 90K deaths globally are associated with exposure to foreign (i.e., originating outside a receptor region) non-dust PM2.5. More than half of the premature mortalities associated with foreign non-dust aerosols are due to aerosols originating from Europe (20K), ME (18K) and EA (15K); and nearly 60% of the 90K deaths occur in EA (21K), IN (19K) and Southeast Asia (16K). The lower and higher bounds of our estimated 95% confidence interval (considering uncertainties from the concentration–response relationship and simulated aerosol concentrations) are 18% and 240% of the estimated deaths, respectively, and could be larger if additional uncertainties were quantified. We find that in 2000 nearly 6.6K premature deaths in North America (NA) were associated with foreign PM2.5 exposure (5.5K from dust PM2.5). NA is least impacted by foreign PM2.5 compared to receptors on the Eurasian continent. However, the number of premature mortalities associated with foreign aerosols in NA (mostly occurring in the U.S.) is comparable to the reduction in premature mortalities expected to result from tightening the U.S. 8-h O3 standard from 0.08 ppmv to 0.075 ppmv. International efforts to reduce inter-continental transport of fine aerosol pollution would substantially benefit public health on the Eurasian continent and would also benefit public health in the United States. 相似文献
1000.
Chongguo Tian Jianmin Ma Liyan Liu Hongliang Jia Diandou Xu Yi-Fan Li 《Atmospheric environment (Oxford, England : 1994)》2009,43(25):3891-3901
Using a dynamic numerical atmospheric transport model for organochlorine pesticides (OCPs), the relationship between the East Asian summer monsoon and the fate of α-hexachlorocyclohexane (α-HCH), a banned OCP, in the atmosphere over Northeast Asia was investigated and assessed. The modeled temporal and spatial patterns and variability of α-HCH air concentrations during the summer months of 2005 revealed a strong link between this chemical in the atmosphere over Northeast Asia and the East Asian summer monsoon. At lower atmospheric levels, easterly and southeasterly winds blowing from relatively cold ocean surface convey α-HCH air concentration from southeast China to northeast China. A monsoon front extending from southeast China to Japan, characterized by a strong wind convergence, carried the air concentration to a high elevation of the atmosphere where it was delivered by southerly monsoon flow to northern China and North Pacific Ocean. This summer monsoon associated northward atmospheric transport caused a reversal of the soil/air exchange from outgassing to net deposition during spring–summer period. The modeled wet deposition fluxes of α-HCH agreed well with the changes in the typical summer monsoon rain bands, designated as Meiyu in China, Changma in Korea, and Baiu in Japan. The major wet deposition flux paralleled with the monsoon front as well as the monsoon rain bands. The temporal change in the fluxes exhibits abrupt northward advances, which is associated with a stepwise northward and northeastward advance of the East Asian summer monsoon. The modeled α-HCH outflow in the atmosphere from China occurs mostly in the summer months and through northeast China, featured strongly by the evolution of the summer month. This study suggests that the East Asian summer monsoon provides a major atmospheric pathway and summer outflows to α-HCH over East Asia. 相似文献