全文获取类型
收费全文 | 9804篇 |
免费 | 365篇 |
国内免费 | 3554篇 |
专业分类
安全科学 | 741篇 |
废物处理 | 645篇 |
环保管理 | 860篇 |
综合类 | 5084篇 |
基础理论 | 1653篇 |
环境理论 | 2篇 |
污染及防治 | 3627篇 |
评价与监测 | 393篇 |
社会与环境 | 319篇 |
灾害及防治 | 399篇 |
出版年
2024年 | 5篇 |
2023年 | 149篇 |
2022年 | 482篇 |
2021年 | 388篇 |
2020年 | 281篇 |
2019年 | 262篇 |
2018年 | 352篇 |
2017年 | 456篇 |
2016年 | 410篇 |
2015年 | 552篇 |
2014年 | 803篇 |
2013年 | 1044篇 |
2012年 | 905篇 |
2011年 | 890篇 |
2010年 | 688篇 |
2009年 | 654篇 |
2008年 | 733篇 |
2007年 | 586篇 |
2006年 | 497篇 |
2005年 | 367篇 |
2004年 | 288篇 |
2003年 | 355篇 |
2002年 | 307篇 |
2001年 | 254篇 |
2000年 | 264篇 |
1999年 | 244篇 |
1998年 | 250篇 |
1997年 | 243篇 |
1996年 | 224篇 |
1995年 | 175篇 |
1994年 | 119篇 |
1993年 | 122篇 |
1992年 | 104篇 |
1991年 | 79篇 |
1990年 | 55篇 |
1989年 | 26篇 |
1988年 | 27篇 |
1987年 | 10篇 |
1986年 | 17篇 |
1985年 | 11篇 |
1984年 | 11篇 |
1983年 | 8篇 |
1982年 | 9篇 |
1981年 | 8篇 |
1975年 | 1篇 |
1974年 | 2篇 |
1973年 | 1篇 |
1972年 | 2篇 |
1971年 | 1篇 |
1968年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 520 毫秒
901.
采用电称冲击低压系统(ELPI)将无烟室和吸烟室内的空气颗粒物(0.03~10.00 μm)分成12级,对其粒子数和质量浓度进行测定.结果表明,吸烟室PM0.03~10.00的日平均粒子数和质量浓度分别是无烟室的1.50、1.13倍.烟草烟雾对室内颗粒物粒子数的影响集中在0.03~1.00 μm粒径段;对室内颗粒物质量浓度的影响表现为双模态结构,峰值分别在0.20~0.70、5.00~8.20 μm粒径段.烟草烟雾颗粒物的粒子数和质量浓度随烟雾消散时间的增加而减少,粒径越小,减小的越明显;烟草烟雾颗粒物在室内消散缓慢,会在长时间内造成影响,应引起足够关注. 相似文献
902.
903.
904.
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
905.
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
906.
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
907.
Jun-Ji Cao Bai-Qing Xu Jian-Qiao He Xian-Qin Liu Yong-Ming Han Ge-hui Wang Chong-shu Zhu 《Atmospheric environment (Oxford, England : 1994)》2009,43(29):4444-4452
Carbonaceous aerosol concentrations were determined for total suspended particle samples collected from Muztagh Ata Mountain in western China from December 2003 to February 2006. Elemental carbon (EC) varied from 0.004 to 0.174 μg m?3 (average = 0.055 μg m?3) while organic carbon (OC) ranged from 0.12 to 2.17 μg m?3 and carbonate carbon (CC) from below detection to 3.57 μg m?3. Overall, EC was the least abundant fraction of carbonaceous species, and the EC concentrations approached those in some remote polar areas, possibly representing a regional background. Low EC and OC concentrations occurred in winter and spring while high CC in spring and summer was presumably due to dust from the Taklimakan desert, China. OC/EC ratios averaged 10.0, and strong correlations between OC and EC in spring–winter suggest their cycles are coupled, but lower correlations in summer–autumn suggest influences from biogenic OC emissions and secondary OC formation. Trajectory analyses indicate that air transported from outside of China brings ~0.05 μg m?3 EC, ~0.42 μg m?3 OC, and ~0.10 μg m?3 CC to the site, with higher levels coming from inside China. The observed EC was within the range of loadings estimated from a glacial ice core, and implications of EC-induced warming for regional climate and glacial ice dynamics are discussed. 相似文献
908.
Min Qin Pinhua Xie Hang Su Jianwei Gu Fumin Peng Suwen Li Limin Zeng Jianguo Liu Wenqing Liu Yuanhang Zhang 《Atmospheric environment (Oxford, England : 1994)》2009,43(36):5731-5742
The temporal behavior of HONO and NO2 was investigated at an urban site in Guangzhou city, China, by means of a DOAS system during the Pearl River Delta 2006 intensive campaign from 10 to 24 July 2006. Within the whole measurement period, unexpected high HONO mixing ratios up to 2 ppb were observed even during the day. A nocturnal maximum concentration of about 8.43 ± 0.4 ppb was detected on the night of 24 July 2006. Combining the data simultaneously observed by different instruments, the coupling of HONO–NO2 and the possible formation sources of HONO are discussed. During the measurement period, concentration ratios of HONO to NO2 ranged from (0.03 ± 0.1) to (0.37 ± 0.09), which is significantly higher than previously reported values (0.01–0.1). Surprisingly, in most cases a strong daytime correlation between HONO and NO2 was found, contrary to previous observations in China. Aerosol was found to have a minor impact on HONO formation during the whole measurement period. Using a pseudo steady state approach for interpreting the nocturnal conversion of NO2 to HONO suggests a non-negligible role of the relative humidity for the heterogeneous HONO formation from NO2. 相似文献
909.
污泥膨胀状态下原生动物群落结构分析 总被引:5,自引:0,他引:5
系统研究了丝状菌膨胀与非丝状菌膨胀2种典型污泥状态下原生动物的群落结构特征及其演变规律。伴随丝状菌的大量增殖,原生动物总量相应减少,匍匐型纤毛虫及有壳类肉足虫数量迅速上升,占据明显的优势地位,典型原生动物为斜管虫(Chilodonella sp.)、小轮毛虫(Trochilia minuta)以及匣壳虫(Centropyxis sp.);非丝状菌污泥膨胀对原生动物总量及种群结构影响较小,伴随粘性菌胶团的大量出现,各功能类群的比例变化较小,但原生动物总量持续增加,其中菌食性纤毛虫呈线性增加,典型原生动物为钟虫(Vorticella sp.)。 相似文献
910.
新型TCAS吸附树脂对水中Cd2+的吸附去除研究 总被引:4,自引:3,他引:1
通过静态吸附试验,研究一种由超分子受体化合物磺化硫杂杯芳烃(TCAS)与树脂结合的产物——新型TCAS吸附树脂对重金属Cd2+的吸附去除性能,并初步探讨了吸附机理。试验研究结果表明,TCAS吸附树脂对Cd2+的饱和吸附量为14.45 mg/g。当温度为20℃,0.5 g TCAS吸附树脂对10 mL浓度为5 mg/L的Cd2+溶液吸附60 min时, Cd2+的去除率可达到99%以上。pH值是影响TCAS吸附树脂吸附效果的重要因素,在pH=5~9时,Cd2+的去除率随着pH值的升高而增大。在试验范围内,TCAS吸附树脂对Cd2+吸附符合Freundlich方程。吸附在TCAS吸附树脂上的Cd2+可洗脱回收,TCAS吸附树脂也可再生利用。 TCAS吸附树脂对重金属Cd2+的吸附机理主要归因于TCAS对Cd2+的络合作用。 相似文献