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881.
Electroreductive dechlorination of chlorophenols with Pd catalyst supported on solidelectrode was studied. As solid electrodes, carbon cloth (CC), carbon felt (CF) and titanium mesh were used, and palladium was plated on solid electrodes by either electrolytic or electroless method. On each electrode with Pd, chlorophenols were qualitatively dechlorinated to phenol, while they were entirely intact on electrodes without Pd. Moreover, neither base electrode nor plating method significantly affected the activity of Pd as far as it was sufficiently loaded on the electrode. Based on the results in the experiments using one electrode repeatedly, Pd catalyst proved to possess a satisfactory duarability under the present condition. It was suggested that the reactive species responsinble for the dechlorination of chlorophenols could be formed during preliminary electrolysis. Thus, (Pd)x-H resulting from the adsorption of electrogenerated hydrogen on metallic Pd might be assumed most probable.  相似文献   
882.
燃煤发电厂SCR脱硝技术原理及催化剂的选择   总被引:4,自引:3,他引:4  
阐述了SCR反应的基本原理,SCR高含尘布置系统主要构成以及选择催化剂应注意的要素。  相似文献   
883.
采用电容耦合等离子体对干空气中的甲烷进行氧化实验,对甲烷的分解效率、反应产物进行了分析。并且和放置催化剂时进行对比,结果表明放置催化剂后,甲烷的分解效率明显提高,反应产物中CO2 的选择性增加。甲烷的最终氧化产物都为CO、CO2 和H2 O。  相似文献   
884.
将Ag-Rh浸渍到共沉淀法合成的Ce-Zr-Al上,制备出Ag(0.04)-Rh(x)/Ce0.5Zr0.5O2-75%Al2O3系列催化剂,采用BET比表面积、X射线衍射光谱(XRD)和原位漫反射傅里叶变换红外光谱(DRIFTS)对催化剂进行表征,并探讨催化剂在贫燃条件下选择性还原NO的活性和反应机理.结果表明,Ag-Rh双组分催化剂的活性较单组分Ag、Rh催化剂的高.Rh负载量为0.7%(质量分数)时,NO转化率达最佳(90.3%),且反应的起燃温度低、活性温度范围宽(300~500℃).DRIFTS结果显示,Rh的添加不仅有利于催化剂表面NO的吸附,而且能促进Ag催化生成关键反应中间体—CO—NH—,进而显著提高NO的转化率.  相似文献   
885.
以实用型太阳能固定膜光催化中试装置对水中大肠杆菌的灭活特性进行了研究.结果表明,太阳能固定膜光催化灭菌包含光催化灭菌和阳光直接灭菌的协同作用,光催化杀菌效果优于阳光的直接杀菌效果.环境扫描电镜分析(ESEM)表明,光催化处理对菌体产生了致命性破坏.光催化灭菌还具有良好的持久性,灭菌处理8 h后,没有出现明显复活再生现象.光催化灭菌速率随循环流速、光强的增大而增大.太阳能固定膜光催化灭菌技术具有良好的应用前景.  相似文献   
886.
• The sustainable approaches related to Fenton sludge reuse systems are summarized. • Degradation mechanism of Fenton sludge heterogeneous catalyst is deeply discussed. • The efficient utilization directions of Fenton sludge are proposed. The classical Fenton oxidation process (CFOP) is a versatile and effective application that is generally applied for recalcitrant pollutant removal. However, excess iron sludge production largely restricts its widespread application. Fenton sludge is a hazardous solid waste, which is a complex heterogeneous mixture with Fe(OH)3, organic matter, heavy metals, microorganisms, sediment impurities, and moisture. Although studies have aimed to utilize specific Fenton sludge resources based on their iron-rich characteristics, few reports have fully reviewed the utilization of Fenton sludge. As such, this review details current sustainable Fenton sludge reuse systems that are applied during wastewater treatment. Specifically, coagulant preparation, the reuse of Fenton sludge as an iron source in the Fenton process and as a synthetic heterogeneous catalyst/adsorbent, as well as the application of the Fenton sludge reuse system as a heterogeneous catalyst for resource utilization. This is the first review article to comprehensively summarize the utilization of Fenton sludge. In addition, this review suggests future research ideas to enhance the cost-effectiveness, environmental sustainability, and large-scale feasibility of Fenton sludge applications.  相似文献   
887.
单原子催化剂不仅实现了对金属原子最大化利用,而且具有较高催化活性和选择性,还是理想的催化理论研究位点,近年来引起了广泛关注。环境催化在环境保护和污染修复中扮演着重要的角色。单原子催化剂在环境催化领域越来越受关注并有望应用于解决环境问题。单原子催化剂研究的重点和难点集中在单原子催化剂可控合成和催化位点分析表征。为推进单原子催化剂在环境催化领域中的应用,本文综述了单原子的主要制备方法和常规表征手段以及单原子催化剂在环境催化中应用的典型案例,并对单原子催化剂在环境催化中的应用将面临的挑战进行了展望。  相似文献   
888.
Catalytic wet air oxidation (CWAO) coupled desalination technology provides a possibility for the effective and economic degradation of high salinity and high organic wastewater. Chloride widely occurs in natural and wastewaters, and its high content jeopardizes the efficacy of Advanced oxidation process (AOPs). Thus, a novel chlorine ion resistant catalyst B-site Ru doped LaFe1-xRuxO3-δ in CWAO treatment of chlorine ion wastewater was examined. Especially, LaFe0.85Ru0.15O3-δ was 45.5% better than that of the 6%RuO2@TiO2 (commercial carrier) on total organic carbon (TOC) removal. Also, doped catalysts LaFe1-xRuxO3-δ showed better activity than supported catalysts RuO2@LaFeO3 and RuO2@TiO2 with the same Ru content. Moreover, LaFe0.85Ru0.15O3-δ has novel chlorine ion resistance no matter the concentration of Cl and no Ru dissolves after the reaction. X-ray diffraction (XRD) refinement, X-ray photoelectron spectroscopy (XPS), transmission electron microscope (TEM), and X-ray absorption fine structure (XAFS) measurements verified the structure of LaFe0.85Ru0.15O3-δ. Kinetic data and density functional theory (DFT) proved that Fe is the site of acetic acid oxidation and adsorption of chloride ions. The existence of Fe in LaFe0.85Ru0.15O3-δ could adsorb chlorine ion (catalytic activity inhibitor), which can protect the Ru site and other active oxygen species to exert catalytic activity. This work is essential for the development of chloride-resistant catalyst in CWAO.
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