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   2313篇
  免费   650篇
  国内免费   985篇
安全科学   200篇
废物处理   101篇
环保管理   108篇
综合类   1625篇
基础理论   1368篇
污染及防治   373篇
评价与监测   117篇
社会与环境   23篇
灾害及防治   33篇
  2024年   10篇
  2023年   67篇
  2022年   101篇
  2021年   130篇
  2020年   99篇
  2019年   91篇
  2018年   187篇
  2017年   217篇
  2016年   233篇
  2015年   254篇
  2014年   256篇
  2013年   286篇
  2012年   293篇
  2011年   233篇
  2010年   259篇
  2009年   209篇
  2008年   168篇
  2007年   137篇
  2006年   135篇
  2005年   103篇
  2004年   75篇
  2003年   64篇
  2002年   55篇
  2001年   45篇
  2000年   43篇
  1999年   35篇
  1998年   22篇
  1997年   30篇
  1996年   15篇
  1995年   25篇
  1994年   17篇
  1993年   19篇
  1992年   11篇
  1991年   6篇
  1990年   5篇
  1989年   3篇
  1988年   2篇
  1986年   3篇
  1985年   3篇
  1983年   1篇
  1980年   1篇
排序方式: 共有3948条查询结果,搜索用时 15 毫秒
801.
本研究先以水浸实现砷碱渣中的砷锑分离,再对水浸渣进行盐酸浸出,得到了可作为工业原料氯化锑溶液.研究结果表明,在液固比为6∶1,温度40℃,浸出时间40 min的条件下,可使水浸过程中锑的浸出率低于3%,砷的浸出率达到99%;盐酸浸出中,控制酸浓度为1∶1,液固比10∶1,温度60℃,浸出时间30 min,能使锑的浸出率达到88%以上.经过水浸和盐酸浸出,锑的直接回收率为85.36%.  相似文献   
802.
Cao J  Zhao C  Huang L  Ding Y  Wang L  Han S 《Chemosphere》2000,40(12):1411-1416
The solubilization of four pairs of substituted indole compounds (SICs) by β-cyclodextrin (β-CD) in water was investigated. The results show that 1,2,3,4-tetrahydrocarbazole and N-methyl-1,2,3,4-tetrahydrocarbazole form 1:1 inclusion complexes with β-CD, while the other six SICs form 1:2 inclusion complexes, respectively. To each pair of SICs with similar structures, the differences between their solubilization in β-CD/water solutions has been explained by the difference of their contact area within the β-CD cavity, the difference of their molecule polarity, or the presence of hydrogen bond between SIC molecule and β-CD molecule.  相似文献   
803.
This work merges kinetic models for α-pinene and d-limonene which were individually developed to predict secondary organic aerosol (SOA) formation from these compounds. Three major changes in the d-limonene and α-pinene combined mechanism were made. First, radical–radical reactions were integrated so that radicals formed from both individual mechanisms all reacted with each other. Second, all SOA model species from both compounds were used to calculate semi-volatile partitioning for new semi-volatiles formed in the gas phase. Third particle phase reactions for particle phase α-pinene and d-limonene aldehydes, carboxylic acids, etc. were integrated. Experiments with mixtures of α-pinene and d-limonene, nitric oxide (NO), nitrogen dioxide (NO2), and diurnal natural sunlight were carried out in a dual 270 m3 outdoor Teflon film chamber located in Pittsboro, NC. The model closely simulated the behavior and timing for α-pinene, d-limonene, NO, NO2, O3 and SOA. Model sensitivities were tested with respect to effects of d-limonene/α-pinene ratios, initial hydrocarbon to NOx (HC0/NOx) ratios, temperature, and light intensity. The results showed that SOA yield (YSOA) was very sensitive to initial d-limonene/α-pinene ratio and temperature. The model was also used to simulate remote atmospheric SOA conditions that hypothetically could result from diurnal emissions of α-pinene, d-limonene and NOx. We observed that the volatility of the simulated SOA material on the aging aerosol decreased with time, and this was consistent with chamber observations. Of additional importance was that our simulation did not show a loss of SOA during the daytime and this was consistent with observed measurements.  相似文献   
804.
采用O3、UV/O3高级氧化法对水中六氯苯(HCB)的降解效果及机理进行了研究,并对结果进行了比较,结果表明,UV本身对HCB的去除率贡献不大,HCB可被O3、UV/O3快速降解,即UV<O3<UV/O3;O3、UV/O3作用时,提高体系的初始pH值不利于HCB的降解,在pH=3,HCB=0.2 mg/L,反应40 min时,HCB的去除可达50%左右,酸性条件下有利于降解反应的进行;无论是O3单独作用还是UV/O3联合作用,HCB的降解基本上满足准一级反应动力学规律,如果体系的pH值基本保持恒定,这种规律就更为明显。根据离子色谱(IC)、GC对六氯苯降解中间产物进行了测定,探讨了O3、UV/O3降解六氯苯的途径和机理。  相似文献   
805.
新型复合球填料为沸石与悬浮球填料的有机组合体,密度约为0.92~0.97g/cm^3,比表面积为711~1185m^2/m^2,表面粗糙,物化性能稳定。在曝气量为20:1,停留时间为6h时,装有新型复合球填料的反应柱挂膜容易,成膜时间短,膜不易脱落,且生物相丰富。膜成熟时对生活污水中的氨氮和COD都有很好的去除效果,出水氨氮浓度≤2mg/L,去除率≥93%;出水COD浓度≤22mg/L,去除率≥80%。新型复合球反应柱在稳定状态处理低浓度的二级出水时,出水氨氮浓度≤2mg/L,去除率89%,出水COD浓度为10~36mg/L,去除率为48%~81%。出水水质符合GB50335-2002标准。  相似文献   
806.
钛基燃烧催化剂的抗硫性能   总被引:1,自引:0,他引:1  
郑柏存  汪仁 《环境化学》1993,12(1):19-23
本文研究了钛基非贵金属燃烧催化剂的硫中毒过程及载体吸硫特性。结果表明,催化剂的抗硫能力与载体吸硫量有关,不同催化剂的抗硫性能为:Cat.3>Cat.4>Cat.5>Cat.1>Cat.2,本文还讨论了硫中毒机理。  相似文献   
807.
Summary. During peak calling activity by male oil palm bunch moths, Tirathaba mundella Walker (Lepidoptera: Pyralidae), their hairpencils, wings or entire body were extracted in hexane. Gas chromatographic-electroantennographic detection (GC-EAD) analyses of hair pencil extracts revealed four compounds that consistently elicited responses from female antennae. The NMR spectrum of isolated compound 1, and mass spectra and retention indices of compounds 1–4 suggested that they were (3S,6S)-2,2,6-trimethyl-6-vinyl-tetrahydro-pyran-3-ol (1), 4-hydroxy-3-methoxy-benzaldehyde (2, vanillin), 6,10,14-trimethyl-2-pentadecanone (3), and 6,10,14-trimethyl-2-pentadecanol (4). Comparative GC and GC-MS analyses of hair pencils extract and synthetic standards confirmed these structural assignments. Moreover, comparative chromatography of synthetic and hairpencil-isolated 1 on a Cyclodex-B column (which separated the four stereoisomers with baseline resolution) revealed that male T. mundella produce the SS-stereoisomer (SS-1). In field cage bioassay experiments in Palembang, Indonesia, synthetic SS-1 and vanillin in combination, but not singly, attracted female T. mundella. SS-1 plus vanillin were as effective as male T. mundella in attracting females. Compounds 3 and 4 did not enhance the blend's attractiveness. Received October 11 2002; accepted March 14, 2003. R1D=" Correspondence to: Gerhard Gries, email: gries@sfu.ca  相似文献   
808.
邻苯二酚2,3-双加氧酶基因克隆、定位和高效表达   总被引:8,自引:2,他引:8  
采用特异性引物,以菲、芘降解菌株ZL5的代谢性质粒为模板,扩增出邻苯二酚2,3—双加氧酶(C23O)基因,将该基因和表达载体pET—30a( )连接,转化E.coli JM109(DE3),获得了高效表达的转化子,SDS—PAGE结果表明,转化子的C23O蛋白不仅在细胞内存在,而且能被分泌到胞外,薄层扫描显示,转化子细胞内和细胞外表达蛋白总量占细胞总蛋白的42%,酶活分析表明,分布在转化子细胞内、外的表达蛋白都具有较高的C23O比活力,Southern杂交将菌株ZL5的C23O基因定位在内生质粒的不同酶切片段上。图5表1参12。  相似文献   
809.
测试了AlCl3,Al2(SO4)3,FeCl3,Fe2(SO4)3等对水的^17O-NMR化学位移和半峰宽的影响。并利用水^17O-NMR化学位移和半峰宽的变化与氢键的关系,分析了AlCl3,Al2(SO4)3。FeCl3,Fe2(SO4)3等对水缔合的影响,研究表明,AlCl3,Al2(SO4)3。FeCl3,Fe2(SO4)3等对水缔合有促进作用。且Fe^3 对水缔合的作用大于Al^3 。  相似文献   
810.
分析了采用叠氮化钠修正法测定水中溶解氧时,对水中亚硝酸根含量与叠氮化钠加入量的关系。  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