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471.
A shortened version of Quick, Easy, Cheap, Effective, Rugged, and Safe method (QuEChERS) for determining the dissipation and residue of imidacloprid present in Zizania latifolia and purple sweet potato was established by using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The average recoveries of imidacloprid in the two crops ranged from 82.12 to 113.79%, with relative standard deviation (RSD) of <7.32%. The dissipation dynamics of imidacloprid in Z. latifolia plants and purple sweet potato plants followed first-order kinetics, with half-lives of 3.2–5.5?days in each of sampling locations. The terminal imidacloprid residues in Z. latifolia and purple sweet potato at each of location were <0.005–0.120?mg kg?1. According to the risk assessment results, both the acute dietary risk quotient and chronic dietary risk quotient values were <1, indicating that imidacloprid is unlikely to pose health risks to humans with normal recommended use. The present study may serve as a valuable reference for the safe and reasonable use of imidacloprid in Z. latifolia and purple sweet potato fields.  相似文献   
472.
Environmental Science and Pollution Research - Natural steroid estrogens (NSEs), including free estrogens (FEs) and conjugated estrogens (CEs), are of emerging concern globally among public and...  相似文献   
473.
ABSTRACT

This paper assesses the evolution of generation technology-mix in Australia, with specific emphasis on understanding how such evolution has been shaped by wider political and socio-economic influences. This assessment is predicated on the argument that the contemporary, quintessentially techno-economic, policy discourse on renewable energy is deficient, as it ignores climacteric political and socio-economic influences on generation technology-mix. The methodological framework employed in this paper is informed by the core tenets of technological change theory. The assessment suggests that generation technology-mix in Australia has historically been overwhelmingly influenced by the underlying technological paradigm of the electricity industry; and that this technological paradigm essentially draws its imprimatur from the wider political and socio-economic contexts. By implication, it suggests that a rapid uptake of renewables will have widespread ramifications, extending into political, socio-economic and cultural realms of a society. Clearly, existing policy discourse – that tends to focus on technical potentials, cost competitiveness, externalities and risks of various renewable technologies – is deficient. A much broader discourse is needed. This paper also made an attempt to develop a basis for such a discourse by reviewing broader aspects of the Australian society that would be affected by a rapid uptake of renewables.  相似文献   
474.
Yang  W.  Deng  D. G.  Meng  X. L.  Zhang  S. 《Russian Journal of Ecology》2019,50(4):352-360
Russian Journal of Ecology - Temporal and spatial variations of phytoplankton community in Lake Erhai were investigated from May 2010 to April 2011. A total of 124 species belonging to 8 phyla and...  相似文献   
475.
Chen  Hui  Mao  Wei  Shen  Yiqiu  Feng  Weiwei  Mao  Guanghua  Zhao  Ting  Yang  Lanqin  Yang  Liuqing  Meng  Chunfeng  Li  Yong  Wu  Xiangyang 《Environmental science and pollution research international》2019,26(24):24609-24619

Phthalates (PAEs) in drinking water sources such as the Yangtze River in developing countries had aroused widespread concern. Here, the water, suspended particulate matter (SPM), and sediment samples were collected from 15 sites in wet and dry seasons in Zhenjiang, for the determination of six PAEs (DMP, DEP, DIBP, DBP, DEHP, and DOP) using the solid-phase extraction (SPE) or ultrasonic extraction coupled with gas chromatography-mass spectrometry (GC-MS). The total concentrations of six PAEs (Σ6PAEs) spanned a range of 2.65–39.31 μg L?1 in water, 1.97–34.10 μg g?1 in SPM, and 0.93–34.70 μg g?1 in sediment. The partition coefficients (Kd1) of PAEs in water and SPM phase ranged from 0.004 to 3.36 L g?1 in the wet season and from 0.12 to 2.84 L g?1 in the dry season. Kd2 of PAEs in water and sediment phase was 0.001–9.75 L g?1 in the wet season and 0.006–8.05 L g?1 in the dry season. The dominant PAEs were DIBP, DBP, and DEHP in water and SPM, DIBP, DEHP, and DOP in sediment. The concentration of DBP in water exceeded the China Surface Water Standard. The discharge of domestic sewage and industrial wastewater might be the main potential sources of PAEs. The risk quotient (RQ) method used for the risk assessment revealed that DBP (0.01 < RQ < 1) posed a medium risk, while DIBP and DEHP (RQ > 1) posed a high environmental risk in water, DIBP (RQ > 1) also showed a high risk in sediment.

  相似文献   
476.
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   
477.
徐正超  刘阳  王世琦  马聪  方峰 《化工环保》2019,39(4):408-412
以季铵盐改性硅藻土为吸油剂,采用吸附—电化学组合工艺处理拉丝废乳化液,优化了工艺条件。实验结果表明,在乳化液pH为5.0、吸油剂加入量为20 g/L、反应温度为25 ℃的最优条件下吸附除油15 min,然后在清液pH为8.5、阳极电流密度为4 A/dm2的最优条件下电化学反应4 h后,废水无色无味,COD为43 mg/L,ρ(NH3-N)=0,ρ(Cu)= 1.6 mg/L,ρ(Zn)= 3.7 mg/L,浊度为1.1 NTU,达到GB 8978—1996污水综合排放标准。  相似文献   
478.
合成了一种高吸附容量的磁性生物炭负载Mg-Fe水滑石复合材料(L-BC),并用于去除水中的Cd2+和Ni2+。表征结果表明,采用浸渍联合热解法成功制备了磁性生物炭(M-BC),水热合成法成功地将Mg-Fe水滑石负载在M-BC上。动力学研究结果表明,Cd2+和Ni2+吸附符合伪二级动力学模型,化学吸附为速率控制步骤。等温吸附研究结果表明,L-BC对Cd2+和Ni2+的吸附符合Langmuir模型,为单分子层化学吸附,最大吸附量分别为263.156 mg/g和43.291 mg/g。吸附机理主要为Mg-Fe水滑石层间CO32-和表面羟基与Cd2+和Ni2+产生表面共沉淀。L-BC具有良好的吸附和重复利用性能,是一种很有前景的去除Cd2+和Ni2+的吸附材料。  相似文献   
479.
化学混凝法去除稠油废水中的硅   总被引:1,自引:0,他引:1  
以新疆油田稠油废水为研究对象,采用化学混凝除硅方法对稠油废水进行处理。实验结果表明:采用锌复合混凝剂的混凝、软化及镁剂除硅相结合的方法具有较好的除硅效果。确定了最佳除硅配方:NaOH的加入量为500~600mg/L,除硅剂MgCl2.6H2O的加入量为700~800mg/L,锌复合混凝剂加入量为100~150mg/L,处理后废水中SiO2的质量浓度小于50mg/L,达到热采锅炉的用水标准。  相似文献   
480.
钢渣吸附Pb2+的动力学研究   总被引:1,自引:0,他引:1  
采用批式振荡吸附法研究了钢渣吸附Pb^2+的动力学。研究结果表明,钢渣吸附Pb^2+的动力学控制步骤(简称动力学控制步骤)随实验条件的变化而变化:钢渣粒径大于120μm、振荡器转速小于150r/min或Pb^2+初始质量浓度小于150mg/L时,孔扩散是动力学控制步骤;钢渣粒径小于120μm、振荡器转速大于150r/min或Pb^2+初始质量浓度大于150mg/L时,表面扩散是动力学控制步骤;钢渣对Pb^2+的吸附反应是二级反应,其吸附速率为13.26g/(mg.min)。  相似文献   
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