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1.
Chen Xiude Chen Guocai Lin Miaoxin Tang Kai Ye Bin 《Environmental geochemistry and health》2022,44(9):2919-2942
Environmental Geochemistry and Health - Rampant corruption exists in China’s energy-intensive industries. However, we know little about the nexus of corruption and enterprise green innovation... 相似文献
2.
建立了便携式顶空/气相色谱-质谱法测定硬质聚氨酯泡沫和组合聚醚中一氟三氯甲烷(CFC-11)、二氟二氯甲烷(CFC-12)、二氟一氯甲烷(HCFC-22)及一氟二氯乙烷(HCFC-141b)的定性分析方法,系统考察了色谱柱、顶空体系、顶空温度和顶空时间对测定结果的影响。结果表明,DB-WAX色谱柱对目标物质的分离效果最好,顶空温度为50℃、顶空时间为10 min条件下,目标物质的检测灵敏度最高。在优化条件下,硬质聚氨酯泡沫取样体积为1 cm3时,4种目标物的方法检出限为0.6~0.8 μg;组合聚醚取样量为10 mg时,4种目标物的方法检出限为0.5~0.6 μg。该方法具有较高的灵敏度,定性准确,适用于实际样品的现场快速定性分析。 相似文献
3.
Y. Chen H. R. Jia S. Niu X. Zhang H. L. Wang Y. Z. Ye Q. S. Chen Z. L. Yuan 《Russian Journal of Ecology》2018,49(1):40-46
Species turnover patterns can be inconsistent due to differences in the dispersal ability of different growth forms. Here, species of trees, shrubs, herbs, and bryophytes in the Xiaoqinling National Nature Reserve in China were analyzed to determine patterns of species turnover along an elevation and spatial gradient. Variance partitioning was used to assess the relative contribution of topographic heterogeneity and dispersal limitation to species turnover. Our results suggest that the effect of dispersal limitation is more important than topographic heterogeneity on species turnover in temperate mountane ecosystems in the study area. Dispersal limitation has a greater effect on trees species turnover than on shrubs, herbs or bryophytes species turnover. 相似文献
4.
Chlorinated ethenes such as trichloroethene (TCE), cis‐1,2‐dichloroethene (cis‐1,2‐DCE), and vinyl chloride along with per‐ and polyfluoroalkyl substances (PFAS) have been identified as chemicals of concern in groundwater; with many of the compounds being confirmed as being carcinogens or suspected carcinogens. While there are a variety of demonstrated in‐situ technologies for the treatment of chlorinated ethenes, there are limited technologies available to treat PFAS in groundwater. At a former industrial site shallow groundwater was impacted with TCE, cis‐1,2‐DCE, and vinyl chloride at concentrations up to 985, 258, and 54 µg/L, respectively. The groundwater also contained maximum concentrations of the following PFAS: 12,800 ng/L of perfluoropentanoic acid, 3,240 ng/L of perfluorohexanoic acid, 795 ng/L of perfluorobutanoic acid, 950 ng/L of perfluorooctanoic acid, and 2,140 ng/L of perfluorooctanesulfonic acid. Using a combination of adsorption, biotic, and abiotic degradation in situ remedial approaches, the chemicals of concern were targeted for removal from the groundwater with adsorption being utilized for PFAS whereas adsorption, chemical reduction, and anaerobic biodegradation were used for the chlorinated ethenes. Sampling of the groundwater over a 24‐month period indicated that the detected PFAS were treated to either their detection, or below the analytical detection limit over the monitoring period. Postinjection results for TCE, cis‐1,2‐DCE, and vinyl chloride indicated that the concentrations of the three compounds decreased by an order of magnitude within 4 months of injection, with TCE decreasing to below the analytical detection limit over the 24‐month monitoring period. Cis‐1,2‐DCE, and vinyl chloride concentrations decreased by over 99% within 8 months of injections, remaining at or below these concentrations during the 24‐month monitoring period. Analyses of Dehalococcoides, ethene, and acetylene over time suggest that microbiological and reductive dechlorination were occurring in conjunction with adsorption to attenuate the chlorinated ethenes and PFAS within the aquifer. Analysis of soil cores collected pre‐ and post‐injection, indicated that the distribution of the colloidal activated carbon was influenced by small scale heterogeneities within the aquifer. However, all aquifer samples collected within the targeted injection zone contained total organic carbon at concentrations at least one order of magnitude greater than the preinjection total organic carbon concentrations. 相似文献
5.
类腐殖质(humic-like substance,HULIS)是一类水溶性、相对分子量高的有机混合物,常见于雾滴、云滴、积雪和大气颗粒物(PM)中.本文主要综述了大气PM中HULIS的提取和分析方法、毒理性、吸光特性和光敏性,重点探讨了PM中有机物和过渡金属(尤其是Fe离子)产生活性氧化性物种(reactive oxygen species,ROS)从而破坏DNA的致毒机理,进一步提出HULIS(含有可逆的氧化还原位点)单独或与过渡金属螯合成有机-金属配体形成ROS的机理.最后对未来大气HULIS的研究方向进行了展望,指出今后应该加强大气HULIS、金属等通过细胞内催生ROS的测定及细胞毒性相关的研究,并关注HULIS的化学结构、分子组分等的定量分析,更好地揭示物质结构与细胞毒性之间的作用机制和关系,以期为大气HULiS的健康影响提供支持. 相似文献
6.
Fu Li Chen Yi Yang Xinyi Yang Zuyao Liu Sha Pei Lei Feng Baixiang Cao Ganxiang Liu Xin Lin Hualiang Li Xing Ye Yufeng Zhang Bo Sun Jiufeng Xu Xiaojun Liu Tao Ma Wenjun 《Environmental science and pollution research international》2019,26(20):20137-20147
Environmental Science and Pollution Research - Fetal growth has been demonstrated to be an important predictor of perinatal and postnatal health. Although the effects of maternal exposure to air... 相似文献
7.
8.
Zhao Yuhuan Cao Ye Shi Xunpeng Zhang Zhonghua Zhang Wenjie 《Environmental science and pollution research international》2021,28(11):13469-13486
Environmental Science and Pollution Research - Electricity generation is the largest sector with decarbonization potential for China and the world. Based on the new emission factors, this paper... 相似文献
9.
为深入研究电气火灾中护套线因过电流诱发短路故障的转化过程,搭建RVVB护套线过电流诱发短路故障电路,统计短路发生概率,借助高速影像,获取短路发生的时间和次数,分析护套线起火燃烧过程。结果表明:在过电流故障发生1 h内,I≤16 A时护套线仅线芯发热、绝缘炭化,无法诱发短路;I=24 A时护套线发生短路概率为40%,在973 s内发生初次短路;32 A≤I<48 A时护套线发生多次短路的概率随电流值增大而增大,在I=48 A时达到50%,发生初次短路的时间随电流值增大而减小,最短时间为28 s;短路引发绝缘层燃烧的概率随电流值增大呈指数递增,I=24 A时护套线在短路后发生燃烧的概率为62.5%,在48 A时达到100%,短路后1 618 ms内火焰可蔓延至护套线两端,形成全线燃烧现象。研究结果可对溯源电气火灾发生的根本原因提供数据支撑。 相似文献
10.