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   4463篇
  免费   429篇
  国内免费   1773篇
安全科学   322篇
废物处理   286篇
环保管理   349篇
综合类   2511篇
基础理论   915篇
污染及防治   1745篇
评价与监测   166篇
社会与环境   160篇
灾害及防治   211篇
  2024年   49篇
  2023年   124篇
  2022年   277篇
  2021年   192篇
  2020年   144篇
  2019年   149篇
  2018年   154篇
  2017年   238篇
  2016年   300篇
  2015年   308篇
  2014年   322篇
  2013年   485篇
  2012年   363篇
  2011年   435篇
  2010年   282篇
  2009年   272篇
  2008年   347篇
  2007年   272篇
  2006年   256篇
  2005年   168篇
  2004年   127篇
  2003年   175篇
  2002年   137篇
  2001年   106篇
  2000年   132篇
  1999年   119篇
  1998年   107篇
  1997年   117篇
  1996年   85篇
  1995年   91篇
  1994年   64篇
  1993年   66篇
  1992年   61篇
  1991年   46篇
  1990年   30篇
  1989年   13篇
  1988年   14篇
  1987年   13篇
  1986年   11篇
  1985年   2篇
  1984年   4篇
  1983年   3篇
  1982年   4篇
  1981年   1篇
排序方式: 共有6665条查询结果,搜索用时 15 毫秒
821.
MSW(城市固体废物)生物反应器型填埋是一种较新颖的方法.在系统分析现有填埋方法优缺点的基础上,对其加以改进,将强制通风好氧和渗滤液循环2种方式有机地结合在一起,构建了MSW好氧生物反应器.考察了NH3、CH4、CO2、pH和温度等因素,并监测分析了渗滤液中的COD、BOD5、Zn^2+、NH4^+和NO3^-等指标,旨在研究其中垃圾的降解及渗滤液中COD、BOD5、Zn^2+、NH4^+和NO3^-的去除情况,探讨该生物反应器对垃圾和渗滤液相关参数的作用机理.结果表明,该反应器对渗滤液中COD、BOD5、NO3^-的去除率分别达到96.34%、94.58%和99.9%,对其中的Zn^2+也有较好的脱除效果.  相似文献   
822.
使用稀释富集法,从大港油田采油废水处理站生化池中定向快速的分离出多株高效石油降解菌株。对分离获得的1株优势菌株进行生理生化和分子生物学鉴定,显示属于Pseudomonas stutzeri的1个新菌株,命名为Pseudomonas stutzeri TH-31。通过批次实验,对菌株TH-31的生长条件和石油降解条件进行了优化,经过条件优化,P.stutzeri TH-31在初始pH 7,原油投加量为300 mg/L,35℃培养5 d后,获得最高石油烃降解率92.7%。  相似文献   
823.
利用化学沉淀法制备磁性四氧化三铁 /石墨烯(Fe3O4 /GE)纳米复合材料,并将其与H2O2构成非均相Fenton体系用于催化降解水中微量的17β-雌二醇(E2),研究了初始pH值,初始H2O2浓度,催化剂用量对E2降解的影响。结果表明,Fe3O4/GE纳米复合材料在无需外加光源的条件下能够有效催化降解E2。在pH 7.0,E2初始浓度为1 mg/L,初始H2O2浓度为15 mmol/L,Fe3O4 /GE投加量为15 mg/L的条件下,反应8 h后可去除92.9%的E2。Fe3O4/GE具有便捷的磁分离特性和稳定的催化活性,经过7次循环使用后对E2的降解效率仍保持在91.5%左右。  相似文献   
824.
RuO2/La2O3/TiO2悬浮体系中直接耐晒黑G的光催化降解   总被引:2,自引:0,他引:2  
钛酸丁酯为前驱体,采用溶胶-凝胶-浸渍法制备RuO2/La2O3/TiO2复合光催化剂,以紫外灯为光源,研究了催化剂组成、煅烧温度、溶液pH值等因素对直接耐晒黑G(DFBG)光催化降解的影响.结果表明掺杂量w(La2O3)1.39%、w(RuO2)0.12%、煅烧温度500℃(2 h)、溶液pH值7.3时,光催化活性最佳.当通气量为200 mL/min,催化剂投加量为150mg时,50 mg/L的DFBG溶液经60 min降解,其降解率近100%.DFBG的光催化降解服从Langmuir-Hinshelwood动力学模型,测得相应的动力学参数k=7.42×10-3mmol/L·min,K=19.54 L/mmol.  相似文献   
825.
In this study, MnO2 and pyrolusite were used as the catalysts to prepare modified activated carbon, that is, AC-Mn and AC-P, respectively, from coals by blending method and steam activation. The Brunauer–Emmett–Teller (BET) results indicated that the AC-P had higher surface areas and micropore volumes than the AC-Mn with the same blending ratio. The relative contents of basic functional groups (i.e., C = O, π-π*) on AC-P were slightly lower than those on AC-Mn, while both contained the same main metal species, namely, MnO. The desulfurization results showed that with 3 wt% of blending ratio, AC-Mn3 and AC-P3 had higher sulfur capacities at 220 and 205 mg/g, respectively, which were much higher than for the blank one (149.6 mg/g). Moreover, the AC-P had relatively higher sulfur capacity than the AC-Mn with the same contents of Mn, which might be attributed to the existence of other metals in pyrolusite. After the desulfurization process, MnO were gradually transferred into MnSO4, and the relative contents of basic functional groups decreased evidently for both AC-Mn3 and AC-P3. The results demonstrated that pyrolusite could be one good alternative to MnO2 to prepare modified activated carbon for desulfurization.

Implications: MnO2 and pyrolusite were used as the additives to prepare modified activated carbon from coals by a blending method and by steam activation, that is, AC-Mn and AC-P, respectively. The AC-P had higher surface areas and micropore volumes than the AC-Mn with the same blending ratio. The AC-Mn and AC-P had higher sulfur capacities than a blank one. Moreover, the AC-P had relatively higher sulfur capacity than the AC-Mn with the same contents of Mn. The results demonstrated that pyrolusite could be one good alternative to MnO2 to prepare modified activated carbon for desulfurizatio.  相似文献   

826.
为解决水体因低碳氮比而导致脱氮效率差的问题,将颗粒聚己内酯(PCL)重新塑形为阶梯环状,研究其作为反硝化过程的生物膜载体与固相碳源的反硝化性能。结果表明,在静态实验中,平均反硝化速率为8.57 mg NO3-N/(L·h);反硝化过程为零级反应。连续填充床实验中,超过90%的硝酸盐可被去除,出水NO2-N质量浓度低于0.20 mg/L;出水NH3-N质量浓度略有上升;出水溶解性有机碳(DOC)先上升后降低至1 mg/L左右。电子扫描显微镜扫描显示,PCL阶梯环反应表面空隙率较高,表面生物膜以杆菌为主,反应后被明显腐蚀;液相色谱检测显示PCL阶梯环分子量反应前后略有下降,其结构未受到破坏;表明该材料适合作为反硝化反应的碳源的同时,又可以作为载体供微生物附着生长。  相似文献   
827.

The response of soil respiration (Rs) to nitrogen (N) addition is one of the uncertainties in modelling ecosystem carbon (C). We reported on a long-term nitrogen (N) addition experiment using urea (CO(NH2)2) fertilizer in which Rs was continuously measured after N addition during the growing season in a Chinese pine forest. Four levels of N addition, i.e. no added N (N0: 0 g N m−2 year−1), low-N (N1: 5 g N m−2 year−1), medium-N (N2: 10 g N m−2 year−1), and high-N (N3: 15 g N m−2 year−1), and three organic matter treatments, i.e. both aboveground litter and belowground root removal (LRE), only aboveground litter removal (LE), and intact soil (CK), were examined. The Rs was measured continuously for 3 days following each N addition application and was measured approximately 3–5 times during the rest of each month from July to October 2012. N addition inhibited microbial heterotrophic respiration by suppressing soil microbial biomass, but stimulated root respiration and CO2 release from litter decomposition by increasing either root biomass or microbial biomass. When litter and/or root were removed, the “priming” effect of N addition on the Rs disappeared more quickly than intact soil. This is likely to provide a point of view for why Rs varies so much in response to exogenous N and also has implications for future determination of sampling interval of Rs measurement.

  相似文献   
828.
Environmental Science and Pollution Research - The prevalence of gestational diabetes mellitus (GDM) is increasing worldwide. Reports of the association between air pollution exposure and GDM have...  相似文献   
829.
Environmental Science and Pollution Research - Hydrothermal liquefaction (HTL) of biomass used HTL reaction under high temperature and pressure to produce bio-oil. This technology is considered as...  相似文献   
830.
Advancements in technology are inextricably bound to our society and the natural environment. However, how the development process of a technology system interacts with both remains unclear. We propose a process model to understand the complex dynamics among technology, society, and the environment via seven interactive elements: technologies, actors, receiving bodies, natural contexts, social contexts, temporal–spatial contexts, and outcomes. The model was applied to agricultural and water technology development in China from 8000 bc to 1911 ad. Our findings show that these elements did not play equally important roles in different periods of the development in ancient China, with social contexts most dominating during the earlier periods and both social and environmental concerns arising towards the later periods. The proposed model, by identifying the elements in the technology development that should be strengthened, can act as an analysis device to assist in reconfiguring a more sustainable socio-technological system.Electronic supplementary materialThe online version of this article (10.1007/s13280-020-01424-7) contains supplementary material, which is available to authorized users.  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