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861.
Liu X  Zhao W  Sun K  Zhang G  Zhao Y 《Chemosphere》2011,82(5):773-777
The conventional hydrothermal reaction with iron powder, NaOH and H2O as reactants was reported to occur at temperature above 423 K, and iron oxides (Fe3O4 and NaFeO2) and hydrogen were produced. In this study, microwave heating was adopted to take the place of conventional heating to induce the hydrothermal reaction. Under microwave irradiation, NaOH and H2O absorbed microwave energy by space charge polarization and dipolar polarization and instantly converted it into thermal energy, which initiated the hydrothermal reaction that involved with zero-valent iron. X-ray diffraction (XRD) analysis found Fe3O4/NaFeO2 and confirmed the occurrence of microwave-induced hydrothermal reaction. The developed microwave-hydrothermal reaction was employed for the dechlorination of PCBs. Hexadecane containing 100 mg L−1 of Aroclor1254 was used as simulative transformer oil, and the dechlorination of PCBs was evaluated by GC/ECD, GC/MS and ion chromatography. For PCBs in 10 mL simulative transformer oil, almost complete dechlorination was achieved by 750 W microwave irradiation for 10 min, with 0.3 g iron powder, 0.3 g NaOH and 0.6 mL H2O added. The effects of important factors including microwave power and the amounts of reactants added, on the dechlorination degree were investigated, moreover, the dechlorination mechanism was suggested. Microwave irradiation combined with the common and cheap materials, iron powder, NaOH and H2O, might provide a fast and cost-effective method for the treatment of PCBs-containing wastes.  相似文献   
862.
Previously, we demonstrated that the concentrations of DDTs were greater in breast milk collected from Chinese mothers than from Japanese and Korean mothers. To investigate dicofol as a possible source of the DDTs in human breast milk, we collected breast milk samples from 2007 to 2009 in China (Beijing), Korea (Seoul, Busan) and Japan (Sendai, Takarazuka and Takayama). Using these breast milk samples, we quantified the concentrations of dichlorobenzophenone, a pyrolysis product of dicofol (simply referred to as dicofol hereafter), dichlorodiphenyltrichloroethane and its metabolites (DDTs) using GC-MS. Overall, 12 of 14 pooled breast milk samples from 210 mothers contained detectable levels of dicofol (>0.1 ng g−1 lipid). The geometric mean concentration of dicofol in the Japanese breast milk samples was 0.3 ng g−1 lipid and significantly lower than that in Chinese (9.6 ng g−1 lipid) or Korean breast milk samples (1.9 ng g−1 lipid) (p < 0.05 for each). Furthermore, the ΣDDT levels in breast milk from China were 10-fold higher than those from Korea and Japan. The present results strongly suggest the presence of extensive emission sources of both dicofol and DDTs in China. However, exposure to dicofol cannot explain the large exposure of Chinese mothers to DDTs because of the trace levels of dicofol in the ΣDDTs. In the present study, dicofol was confirmed to be detectable in human breast milk. This is the first report to identify dicofol in human samples.  相似文献   
863.
Zhang J  Liu SS  Dou RN  Liu HL  Zhang J 《Chemosphere》2011,82(7):1024-1029
Ionic liquids (ILs) are a fascinating group of new chemicals with the potential to replace the classical volatile organic solvents, stimulating many applications in chemical industry. In case ILs are released to the environment, possible combined toxicity should be taken into account and it is, however, often neglected up to now. In this paper, therefore, the concentration-response curves (CRCs) of four groups of IL mixtures with various mixture ratios to Vibrio qinghaiensis sp.-Q67 were determined using the microplate toxicity analysis and were compared to the CRCs predicted by an additive reference model, the concentration addition (CA) or independent action (IA), to identify the toxicity interaction. It is showed that most of the IL mixture rays displayed the classical addition while the remaining rays exhibited antagonism or synergism. Moreover, it is found that the pEC50 values of the mixture rays exhibiting antagonism or synergism are well correlated with the mixture ratio of a certain IL therein.  相似文献   
864.
Liu YP  Li JG  Zhao YF  Wen S  Huang FF  Wu YN 《Chemosphere》2011,83(2):168-174
The levels of polybrominated diphenyl ethers (PBDEs) and indicator polychlorinated biphenyls (PCBs) were determined in marine fish from four areas of China (South China Sea, Bohai Sea, East China Sea, and Yellow Sea) using GC/NCI-MS and GC/ITMS, respectively. Total concentrations of eight PBDEs (BDE-28, 47, 99, 100, 153, 154, 183 and 209) in all samples ranged from 0.3 ng g−1 ww (wet weight) to 700 ng g−1 ww, with median and mean values of 85 ng g−1 ww and 200 ng g−1 ww, respectively. BDE-209 and BDE-47 were the major congeners in all samples, contributing 54% and 19% to the total concentration, respectively. The sum of seven indicator PCB levels (CB-28, 52, 101, 118, 138, 153, and 180) ranged from 0.3 ng g−1 ww to 3.1 μg g−1 ww, with median and mean values of 6.4 ng g−1 ww and 398 ng g−1 ww, respectively. High contributions of CB-138 (32%) and CB-153 (25%) were found in all samples. In general, pollutants measured in this study were at high levels when compared with previous studies from other regions in the world. The relative abundance of BDE-209 may suggest that deca-BDE sources existed in studied area. And principal component analysis (PCA) showed that there were other PBDE sources in Yellow Sea. The pattern and PCA showed that PCB pollutions came from similar sources in the studied areas. In addition, concentrations of ∑7PBDEs (u/209) were strongly correlated with those of ∑7PCBs in all fish (r = 0.907, n = 44).  相似文献   
865.
从规划内容与目标、规划方法及方案实施和评估3方面对太湖近20年水污染物控制历程进行综合分析,认为太湖水污染物控制正处面源污染、生活污染及新型污染问题凸显且更难处理,更为广泛的利益相关者和科研队伍积极参与的转型期.这种变化将导致污染治理面临更难应付的动态性和复杂性,使得当前以环境容量为总量为指导通过自上而下分配排污量和削减量的控制方案面临极大挑战.结合太湖水污染现状,通过与现行治理方法在管理假设、适合对象、协调管理手段、管理目标、规划方法、公众参与程度以及规划的优劣势等方面的比较发现,适应性管理可以积极有效应对由于环境趋势和管理协调对象变化所带来的系统不确定性和复杂性,将是一个积极有效的补充方法.同时,本文基于适应性管理提出了太湖水环境污染物排放控制体系的构建框架,突出适应性管理平台、科学研究及公众与基层单位参与在污染物控制中的重要作用.  相似文献   
866.
基于空间计量经济学的碳排放与经济增长分析   总被引:8,自引:0,他引:8  
本文采用空间计量经济学的方法对我国各省份的经济增长与碳排放之间的关系进行了实证分析,结果表明:我国各省份的碳排放在空间分布上表现出一定的空间正自相关性,碳排放量最高的省份多处于经济发达的沿海地区,如以北京为中心的环渤海地区,以上海为中心的长三角地区和以广东为核心的珠三角地区,而次之的是经济较为发达的地区,如中部的山西、湖北、湖南、江西、安徽和西南地区;我国各省份的碳排放在空间分布上存在一定的空间集群效应,如环渤海地区就表现出高碳排放的空间集群效应,而西部地区的西藏、新疆、甘肃、青海却表现出低碳排放的空间集群效应.经济增长与碳排放呈现出正相关关系,高碳排放的地区多处于经济发达的沿海地区,而低碳排放的地区多处于经济落后的内陆地区;我国目前的经济增长对碳排放的依赖性较强,经济增长对碳排放的弹性系数约为0.8左右,说明在未来的短时间内很难实行低碳经济的发展模式.  相似文献   
867.
The five central cities-Beijing,Tianjin,Shanghai,Guangzhou and Shenzhen-of the three most important strategic regions in China,namely Beijing-Tianjin-Hebei metropolitan region,the Yangtze River Delta and the Pearl River Delta,are taken as a comparative analysis on urban producer services’ competitiveness,especially focusing on the comparative advantages and disadvantages of producer services in Beijing.Firstly,based on an integrated indicator system including one objective hierarchy,four standard hierarchies and 35 indicator hierarchies,the study applies factor analysis model and analytic hierarchy process model reformed by entropy technology to measure the comprehensive competitiveness of producer services in the above five cities.Secondly,Beijing has comparative advantages of capital resource,industrial base,scientific research resource and market scale,since it takes the first place of the five cities in the comprehensive competitiveness of producer services,the competitiveness of industrial development,business environment and living environment,only inferior to Shanghai in the competitiveness of talent capital.Thirdly,Beijing has comparative disadvantages in the level of producer services development,urban innovation capability and living environment.Finally,five proposals are put forth to enhance the competitiveness of producer services in Beijing,namely perfecting the system of laws and statutes,supporting the development of industry association,implementing scientific development planning,introducing preferential fiscal and taxation policies and strengthening human capital reserve.  相似文献   
868.
In the present study, five soil samples with organic carbon contents ranging from 0.23% to 7.1% and aged with technical dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) for 15 months were incubated in a sealed chamber to investigate the dynamic changes of the OCP residues. The residues in the soils decreased over the incubation period and finally reached a plateau. Regression analysis showed that degradable fractions of OCPs were negatively correlated with soil organic carbon (SOC) except for α-HCH, while no correlation was found between degradation rate and SOC, which demonstrated that SOC content determines the OCP sequestration fraction in soil. Analysis of the ratio of DDT and its primary metabolites showed that, since it depends on differential sequestration among them, magnitude of (p,p′-DDE + p,p′-DDD)/p,p′-DDT is not a reliable criterion for the identification of new DDT sources.  相似文献   
869.
The distribution and bioaccumulation of steroidal and phenolic endocrine disrupting chemicals (EDCs) were studied in various tissues of wild fish species from Dianchi Lake, China. In muscle tissue, 4-tert-octylphenol, 4-cumylphenol, 4-nonlyphenol and bisphenol A were detected in fish from each sampling site, with maximal concentrations of 4.6, 4.4, 18.9 and 83.5 ng/g dry weight (dw), respectively. Steroids (estrone, 17β-estradiol 17α-ethynylestradiol and estriol) were found at lower levels (<11.3 ng/g dw) and less frequently in muscle samples. The highest concentrations of steroids and phenols were found in liver, followed by those in gill and the lowest concentration was found in muscle. The field bioconcentration factors (BCFs) of phenols were calculated in fish species ranged from 18 to 97. Moreover, the measured tissue concentrations were utilized in order to estimate water concentration of steroids (4.4-18.0 ng/L). These results showed that steroidal and phenolic EDCs were likely ubiquitous contaminants in wild fish.  相似文献   
870.
A monoclonal antibody-based competitive antibody-coated enzyme-linked immunosorbent assay (ELISA) was developed and optimized for determining chlorpyrifos residue in agricultural products. The IC(50) and IC(10) of this ELISA were 3.3 ng/mL and 0.1 ng/mL respectively. The average recoveries in six agricultural products were between 79.5% and 118.0%, with the intra-assay coefficient of variation being less than 8 %. The limit of detection for all tested products was 30 ng/g. To the best of our knowledge, this assay has the best specificity among all the published research on ELISAs for chlorpyrifos.  相似文献   
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