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131.
132.
采用水蒸气、氨气、过氧化氢气雾和臭氧4种气体对沙林模拟剂氟磷酸二异丙酯(DFP)进行降解研究,发现臭氧对DFP具有较好的降解作用,在流量200 L/h,DFP初始浓度50 mg/m3时,降解率最高可达56.1%。对高浓度DFP(大于80 mg/m3)进行降解研究时,等离子体单独作用最高降解率为89%,而添加臭氧后的降解率都在95%以上。计算得到臭氧作用的能量利用率为0.05 mg/(W·h),等离子体的能量利用率为0.55 mg/(W·h),而添加臭氧后的等离子体能量利用率为0.68 mg/(W·h)明显高于臭氧和等离子体能量利用率之和,因此对高浓度DFP进行处理时,臭氧与等离子体存在耦合作用。对等离子体和臭氧耦合等离子体降解DFP反应进行了产物分析,发现主要的降解产物基本一致,但是臭氧的存在能使降解更加彻底。 相似文献
133.
Ying Wang Juying Wang Jingli Mu Zhen Wang Ziwei Yao Zhongsheng Lin 《Environmental science and pollution research international》2014,21(1):148-158
Predicted no-effect concentration (PNEC) is often used in ecological risk assessment to determine low-risk concentrations for chemicals. In the present study, native marine species were selected for toxicity testing. The PNECs for three polycyclic aromatic hydrocarbons (PAHs), specifically phenanthrene (Phe), pyrene (Pyr), and benzo[a]pyrene (BaP), were derived from chronic and acute toxicity data with log-normal statistical methods. The achieved PNECs for Phe, Pyr, and BaP were 2.33, 1.09, and 0.011 μg/L, respectively. In Jinzhou Bay and the Shuangtaizi River Estuary of Liaodong Bay in the Bohai Sea, China, the surface water concentrations of the three PAHs were analyzed by gas chromatography–mass spectrometry. Based on two probabilistic ecological risk assessment (PERA) methods, namely probabilistic risk quotient and joint probability curve, the potential risk of Phe, Pyr, and BaP in Jinzhou Bay and Shuangtaizi River Estuary was assessed. The same order of ecological risk (BaP > Phe > Pyr) was found by both models. Our study considered regional characteristics of marine biota during the calculation of PNECs, and the PERA methods provided probabilities of potential ecological risks of chemicals. Within the study area, further research on BaP is required due to its high potential ecological risk. 相似文献
134.
石英砂滤料表面润湿改性 总被引:2,自引:0,他引:2
采用硅烷偶联剂、钛酸酯偶联剂和铝酸酯偶联剂对石英砂进行表面改性,以制备亲油疏水性滤料。研究得出,钛酸酯偶联剂改性石英砂的最佳工艺条件为:偶联剂用量15%,反应温度90℃,搅拌时间15 min;硅烷偶联剂和铝酸酯偶联剂改性石英砂的最佳工艺条件均为:偶联剂用量15%,反应温度110℃,搅拌时间15 min。水对钛酸酯偶联剂改性石英砂滤料的润湿重量由改性前的1.5589 g降低到0.0282 g,水对硅烷偶联剂改性石英砂滤料的润湿重量降低到0.0607 g,水对铝酸酯改性石英砂滤料的润湿重量降低到0.2664 g。静态吸附实验表明,硅烷偶联剂、钛酸酯偶联剂和铝酸酯偶联剂改性石英砂滤料对油的吸附容量分别增加了33.67%、42.87%和22.30%。XPS和FT-IR分析表明,偶联剂均以化学键的方式包覆在石英砂滤料表面,结合稳定。 相似文献
135.
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137.
Climate change and human disturbance drive catchment erosion and increase riverine sediment load sensitively in small and
medium-sized watersheds. This is not always true in large basins, where aggregation and buffering effects have dampen the
ability to determine the driving forces of sedimentation. Even though there are significant responses to sedimentation in
large river basins, it is difficult to get a precise quantitative assessment of specific drivers. This paper develops a methodology
to identify driving forces that change suspended sediment load in the Upper Yangtze river. Annual runoff and sediment load
data from 1954 to 2005 at the Yichang gauging station in the Upper Yangtze basin, daily precipitation data from 60 meteorological
stations, and survey data on reservoir sediment were collected for the study. Sediment load/rainfall erosivity (S/R), is a
new proxy indicator introduced to reflect human activities. Since the mid-1980s, S/R in the Upper Yangtze has dramatically
declined from 0.21 to 0.03 (×1010 t ha h MJ−1 mm−1), indicating that human activity has played a key role in the decline of the suspended sediment load. Before the mid-1980s,
a higher average S/R is attributed to large-scale deforestation and land reclamation. A significant sediment decrease occurred
from 1959 to 1961 during an extreme drought condition, and an increase in sedimentation in 1998 coincided with an extreme
flood event, which was well recorded in the S/R curve. This indicates that the S/R proxy is able to distinguish anthropogenic
from climate impacts on suspended sediment load, but is not necessarily indicatory in extreme climate events. In addition,
typical drivers of riverine sediment load variation including soil conservation projects, reservoirs construction, and land
use/cover change are discussed. 相似文献
138.
火电燃料消费过程对资源环境的影响评估 总被引:2,自引:0,他引:2
杨振 《长江流域资源与环境》2011,20(2):239-243
我国以化石能源为主要燃料的火电生产导致了严重的资源枯竭和环境污染问题,定量评估火电燃料消费对资源环境的影响是区域可持续发展研究的重要内容。在估算火电燃料燃烧及运输、生产过程中排放的主要大气污染物的基础上,利用成分法计算相应的生态足迹,定量评估火电燃料消费过程对资源环境的影响。结果表明:我国1 kW〖DK〗·h火电的燃料消费过程中排放的CO2、CH4、NOx、SO2、烟尘分别为107 kg、993×10-3 kg、646×10-3 kg、260×10-3 kg、202×10-2 kg;全国火电燃料消费占用的生态足迹由2000年的50 67444万hm2,增加到2007年的123 84208万hm2,年均增长1362%;CO2和NOx的生态足迹平均比重高达836%,是影响资源环境的主要因子,SO2、烟尘与CH4三者合计仅164%,对资源环境的冲击相对较小 相似文献
139.
Dechlorane Plus (DP) has been determined in surface sediments from three Chinese coastal bays, e.g. Jiaozhou, Sishili and Taozi Bay in North China. DP concentrations ranged from <1.2 to 187 pg g−1 dry weight (dw) (mean: 24.7 pg g−1 dw) in Jiaozhou Bay, <1.2 to 135 pg g−1 dw (mean 69.9 pg g−1 dw) in Sishili Bay and <1.2 to 66.7 pg g−1 dw (mean: 40.4 pg g−1 dw) in Taozi Bay, respectively. Additionally, two dechlorinated species were quantified, which accounted for 0.6-5.1% of the ∑DP concentration.The fsyn values (syn-isomer/(syn- + anti-isomer)) in sediments from Jiaozhou Bay (mean 0.29) were close to the technical DP mixture (0.2-0.4), probably indicating local inputs of DP. In contrast, sediments in Sishili and Taozi Bay showed much lower fsyn values (mean 0.16). During transportation the DP isomers are subject to stereo selective degradation which partly resulted in the relative enrichment of anti-DP in coastal sediments. 相似文献
140.