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1.
基于中国资源型城市2003—2018年面板数据综合测度城市转型绩效,采用空间马尔科夫链、空间计量模型和空间双重差分模型,探究资源型城市转型绩效特征及其对碳排放的影响。结果表明:(1)资源型城市转型绩效逐渐提升,与此对应的是区域差异呈波动上升趋势,且四种类型资源型城市之间区域差异主要来源于地区内差异,成熟型城市贡献最大;资源型城市转型绩效存在明显的空间分异性,发展格局由以跨越区为核心的“多点式”零星分布向先行区为核心的“组团式”聚集形态演变。(2)资源型城市转型绩效在不同时期存在状态转移的可能性,具有滞后区、起步区、跨越区和先行区4个趋同俱乐部特征,空间马尔科夫链表明转移趋势存在明显空间关联性,状态转移通常出现在相邻等级之间,较少有“跳跃式”转移现象,具有长期性和持续性特征。(3)资源型城市转型具有显著碳减排效应,而且这种效应存在不同资源类型、不同发展阶段和不同空间区位的异质性特征,经济产业转型、社会生活转型和生态环境转型是发挥碳减排效应的重要因素;进一步的政策冲击分析表明,产业转型升级示范区和高新技术产业开发区的设立对城市碳减排具有积极的政策效应。  相似文献   
2.
• Pore structure affects biologically activated carbon performance. • Pore structure determines organic matter (OM) removal mechanism. • Microbial community structure is related to pore structure and OM removal. Optimizing the characteristics of granular activated carbon (GAC) can improve the performance of biologically activated carbon (BAC) filters, and iodine value has always been the principal index for GAC selection. However, in this study, among three types of GAC treating the same humic acid-contaminated water, one had an iodine value 35% lower than the other two, but the dissolved organic carbon removal efficiency of its BAC was less than 5% away from the others. Iodine value was found to influence the removal of different organic fractions instead of the total removal efficiency. Based on the removal and biological characteristics, two possible mechanisms of organic matter removal during steady-state were suggested. For GAC with poor micropore volume and iodine value, high molecular weight substances (3500–9000 Da) were removed mainly through degradation by microorganisms, and the biodegraded organics (soluble microbial by-products,<3500 Da) were released because of the low adsorption capacity of activated carbon. For GAC with higher micropore volume and iodine value, organics with low molecular weight (<3500 Da) were more easily removed, first being adsorbed by micropores and then biodegraded by the biofilm. The biomass was determined by the pore volume with pore diameters greater than 100 μm, but did not correspond to the removal efficiency. Nevertheless, the microbial community structure was coordinate with both the pore structure and the organic removal characteristics. The findings provide a theoretical basis for selecting GAC for the BAC process based on its pore structure.  相似文献   
3.
为了对比径向外喷和轴向喷雾下的低阻文丘里振弦栅耦合除尘效果,以除尘效率和系统阻力为参照,选定喉管气速、振弦栅数、纤维丝间隙和喉管液气比进行单因素实验。结果表明2种喷雾方式的除尘效率和系统阻力的变化趋势相同。利用SPSS软件进行4因素3水平正交实验设计,在特定参数条件下,2种喷雾方式的因素影响排序相同,除尘效率为纤维栅数>纤维丝间隙>喉管气速>喷雾量;系统阻力为喉管气速>纤维栅数>纤维丝间隙>喷雾量;径向外喷最佳配置为喉管气速24 m/s、喷雾量2.3 L/min、2块间隙为0.8 mm纤维栅板;轴向喷雾为喉管气速28 m/s、喷雾量2.4 L/min、2块间隙为0.8 mm纤维栅板;在最优配置下的除尘性能为径向外喷>轴向喷雾。  相似文献   
4.
重金属对人体的显著毒性和难降解的特性,使重金属水体污染成为全球性关注的环境问题。本文综述了重金属废水的危害、来源及常用处理方法,比较了不同类型活性炭处理废水中重金属离子的差异,阐述了不同类型活性炭处理技术的优势和特点,并对今后的重金属废水处理技术研究方向进行了展望。  相似文献   
5.
李楠  王鹏  宋伦  邵泽伟  赵海勃 《化工环保》2018,38(3):300-304
以颗粒活性炭(GAC)为载体、铜为活性组分、铈为助剂组分、草酸钠为沉淀剂,采用浸渍焙烧法制得CuO_x-CeO_2/GAC催化剂。以H_2O_2为氧化剂,微波强化催化湿式过氧化氢氧化(CWPO)处理二甲亚砜(DMSO)初始质量浓度为1 000 mg/L的废水,处理3 min后DMSO去除率达93.8%。催化剂第7次使用时DMSO去除率仍保持在75%以上。初始废水pH在3~9范围内,DMSO去除率均在85%以上。助剂Ce的加入提高了催化剂表面活性组分的分散性和稳定性,使催化剂的活性稳定性和使用寿命显著提高。  相似文献   
6.
三维电极电Fenton氧化法处理染料废水   总被引:1,自引:0,他引:1       下载免费PDF全文
采用三维电极电Fenton氧化法处理实际染料废水,探究了染料废水处理效果的影响因素。实验结果表明:以钌铱镀层钛电极为阳极、不锈钢板为阴极、粉末活性炭为颗粒电极,在粉末活性炭投加量为2.0 g/L、电流密度为0.5 mA/mm2、极板间距为3 cm、pH为2.0、硫酸亚铁投加量为0.50 g/L的最优工艺条件下,反应2 h后COD、TOC、氨氮、色度的去除率达到最大,分别为62.80%、41.15%、42.48%和95.00%;粉末活性炭作为颗粒电极可使染料废水COD去除率提高18个百分点;重复使用10次的处理效果与第2次基本持平。  相似文献   
7.
Biomethane production through biogas upgrading is a promising renewable energy for some industries which could be part of the equilibrium needed with fossil fuels consumption to achieve a sustainable society. This paper presents a comprehensive list of biogas upgrading technologies focused on carbon dioxide removal as well as recent advances reported by researcher with wide expertise in this topic. Additionally, an extensive costs–performance comparison among the technologies studied is discussed. Among the different alternatives, chemical scrubbing stood out to achieve high biomethane purities while cryogenic technologies proved to be effective against methane losses. Regarding the different costs, water scrubbing and membrane separation seem to be the most affordable techniques.  相似文献   
8.
We exploit recent advances in climate science to develop a physically consistent, yet surprisingly simple, model of climate policy. It seems that key economic models have greatly overestimated the delay between carbon emissions and warming, and ignored the saturation of carbon sinks that takes place when the atmospheric concentration of carbon dioxide rises. This has important implications for climate policy. If carbon emissions are abated, damages are avoided almost immediately. Therefore it is optimal to reduce emissions significantly in the near term and bring about a slow transition to optimal peak warming, even if optimal steady-state/peak warming is high. The optimal carbon price should start relatively high and grow relatively fast.  相似文献   
9.
10.
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   
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