首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   495篇
  免费   89篇
  国内免费   363篇
安全科学   44篇
废物处理   150篇
环保管理   42篇
综合类   441篇
基础理论   76篇
污染及防治   190篇
评价与监测   1篇
社会与环境   3篇
  2024年   1篇
  2023年   17篇
  2022年   25篇
  2021年   29篇
  2020年   27篇
  2019年   27篇
  2018年   49篇
  2017年   35篇
  2016年   51篇
  2015年   58篇
  2014年   60篇
  2013年   42篇
  2012年   55篇
  2011年   35篇
  2010年   24篇
  2009年   32篇
  2008年   28篇
  2007年   39篇
  2006年   42篇
  2005年   34篇
  2004年   34篇
  2003年   26篇
  2002年   24篇
  2001年   27篇
  2000年   18篇
  1999年   23篇
  1998年   20篇
  1997年   8篇
  1996年   13篇
  1995年   10篇
  1994年   10篇
  1993年   7篇
  1992年   7篇
  1991年   4篇
  1990年   1篇
  1989年   2篇
  1988年   2篇
  1987年   1篇
排序方式: 共有947条查询结果,搜索用时 62 毫秒
791.
以三乙胺为氮源,HF为形貌控制剂,采用水热法一步合成了N掺杂(001)面锐钛矿TiO_2纳米片/还原氧化石墨烯(N-Ti O2/RGO)复合催化剂,通过XRD、FTIR、SEM、TEM和Raman对样品的组成结构和形貌进行表征。以罗丹明B(Rh B)为模拟污染物,研究了不同掺N量和氧化石墨烯加入量下制备的复合材料的光催化性能。实验结果表明:当n(N)∶n(Ti)为0.5,氧化石墨烯加入量为15 m L时,N-TiO)2/RGO复合材料的光催化性能最好。在催化剂用量为0.5 g/L,罗丹明B溶液初始浓度为20 mg/L时,紫外光催化反应30 min后,罗丹明B的降解率可达94.02%。  相似文献   
792.
废SCR脱硝催化剂中钨和钒的浸出实验研究   总被引:1,自引:0,他引:1  
废SCR脱硝催化剂中钨和钒的浸出是实现其回收的关键.采用碳酸钠混合焙烧-稀硫酸浸出法,对废SCR脱硝催化剂中金属钨和钒的浸出实验进行了研究,考察了焙烧温度t_1(℃)、焙烧时间t_2(h)、硫酸浓度c(v/v)、液固比w、浸出温度t_3(℃)、浸出时间t_4(h)、Na_2CO_3与催化剂的质量比m(Na_2CO_3)/m(催化剂)等因素对钨和钒浸出率的影响.结果表明,在t_1为800℃、t_2为3 h、c为2%、w为8:1、t_3为80℃、t_4为4 h、m(Na2CO3)/m(催化剂)为1.2的反应条件下,废SCR脱硝催化剂中钨和钒的浸出率可分别高达99.08%、98.49%,为后续钨和钒的高效提取与回收提供了有利的条件.  相似文献   
793.
An environmentally benign, simple, and efficient process has been developed for biodiesel production from waste olive oil in the presence of a catalytic amount of TiO2 nanoparticles at 120°C with a conversion of 91.2% within 4 h. The present method affords nontoxic and noncorrosive medium, high yield of biodiesel, clean reaction, and simple experimental and isolation procedures. The catalyst can be recycled by simple filtration and reused without any significant reduction in its activity.  相似文献   
794.
Spent mushroom compost (SMC) is a co-product of edible mushroom which contains abundant nutrients including organics, nitrogen (N) and phosphorous (P). This study is related to the release potential of nitrogen, phosphate and organic matter from SMC amended soil in column-based experiments. Results showed that due to SMC application, NH4+–N and NO3–N concentrations in leachate decreased by 92.5% and 76.3%, respectively, while EC and CODCr concentrations increased by 84.2% and 481.9%, respectively, as compared to chemical fertilizers. Moreover, a minor loss of TNcum (65%) and TPcum (almost equal value) exhibited good nutrient retention capacity. Leaching test results demonstrated that the mixed application of SMC and chemical fertilizers could alleviate excessive CODCr level in SMC leachate. The release process of nutrients in SMC amended soil could be described by first/first order mixed model, indicating that nutrients leached from SMC follow a two-stage pattern.  相似文献   
795.
Experiments were conducted in a fixed-bed reactor that contained a commercial catalyst, V2O5–WO3/TiO2, to investigate mercury oxidation in the presence of NO and O2. Mercury oxidation was improved by NO, and the efficiency was increased by simultaneously adding NO and O2. With NO and O2 pretreatment at 350°C, the catalyst exhibited higher catalytic activity for Hg0 oxidation, whereas NO pretreatment did not exert a noticeable effect. Decreasing the reaction temperature boosted the performance of the catalyst treated with NO and O2. Although NO promoted Hg0 oxidation at the very beginning, excessive NO counteracted this effect. The results show that NO plays different roles in Hg0 oxidation; NO in the gaseous phase may directly react with the adsorbed Hg0, but excessive NO hinders Hg0 adsorption. The adsorbed NO was converted into active nitrogen species (e.g., NO2) with oxygen, which facilitated the adsorption and oxidation of Hg0. Hg0 was oxidized by NO mainly by the Eley–Rideal mechanism. The Hg0 temperature-programmed desorption experiment showed that weakly adsorbed mercury species were converted to strongly bound ones in the presence of NO and O2.  相似文献   
796.
Co、Ni掺入对Pd-Rh型催化剂三效净化C_3H_8、CO、NO的影响   总被引:1,自引:1,他引:0  
以堇青石质陶瓷蜂窝为第一载体,活性氧化铝和铈锆复合氧化物固溶体涂层为第二载体,采用等体积浸渍法制备系列低Pd-Rh含量的三效催化剂及Co、Ni单或双掺入样品。主要研究了Co、Ni掺入对Pd-Rh型催化剂三效净化C3H8、CO、NO活性的影响,结果表明:同时掺入Co、Ni催化剂的三效净化效果优于单独掺入Co或Ni的三效净化效果,同时掺入Co、Ni时,掺入1%Co3O4和2%Ni O的催化剂净化效果最佳;350℃时,催化脱除C3H8、CO的效率分别为100%、97%,400℃时,催化脱除NO的效率为99%。  相似文献   
797.
针对目前关键装置要害部位的安全技术报告中只进行定性评估的不足,运用模糊层次分析法对催化裂化装置进行了评价,评价结果对改进关键装置要害部位安全管理提供了决策依据.  相似文献   
798.
The low-heat-value cornstalk gas produced in the down-flow fixed bed gasifier was tentatively used for methanol synthesis. The cornstalk gas was purified and the technical procedures such as deoxygenation, desulfurization, catalytic cracking of tar, purification and hydrogenation were studied. The catalytic experiments of methanol synthesis with cornstalk syngas were carried out in a tubular-flow integral and isothermal reactor. The effect of reaction temperature, pressure, catalyst types, catalyst particle size, syngas flow at entering end and composition of syngas was investigated. The optimum process conditions and yield of methanol from cornstalk syngas were obtained. The experimental results indicated that the proper catalyst for the synthetic reaction was C301 and the optimum catalyst size was 0.833 mm x 0.351 mm. The optimum operating temperature and pressure were found to be 235癈 and 5 MPa, respectively. The suitable syngas flow 0.9-1.10 mol/h at entering end was selected and the best composition of syngas were CO 10.49%, CO2 8.8%, N2 37.32%, CnHm 0.95% and H2 40.49%. The best methanol yield was 0.418 g/g cornstalk. This study provided the technical support for the industrial test of methanol production from biomass (cornstalk) gas.  相似文献   
799.
本文研究了失活甲醇催化剂用于脱除硫化氢的试验。结果表明,失活甲醇催化剂具有较好的脱硫性能,其重量硫容在室温和623K时稍低于工业氧化锌脱硫剂,在423K-523K的温度范围内则大于工业氧化锌脱硫剂,其体积硫容在室温下大于工业氧化锌脱硫剂,失活甲醇催化剂的工作硫容随着的升高而增长,而且在低反应空速时或者经过还原后具有更大的硫容。  相似文献   
800.
陈敏  郑小明 《环境化学》2000,19(2):110-113
采用共沉淀法制备了一系列不同摩尔比的银铁复合氧化物催化剂。采用XRD,TPD-MS,TPR等技术以及CO氧化反应考察银了铁复合氧化物催化剂的结构和表面氧性质。  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号