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   216篇
  免费   44篇
  国内免费   199篇
安全科学   29篇
废物处理   17篇
环保管理   15篇
综合类   264篇
基础理论   57篇
污染及防治   69篇
评价与监测   5篇
社会与环境   1篇
灾害及防治   2篇
  2024年   1篇
  2023年   4篇
  2022年   7篇
  2021年   11篇
  2020年   17篇
  2019年   17篇
  2018年   15篇
  2017年   6篇
  2016年   20篇
  2015年   23篇
  2014年   21篇
  2013年   48篇
  2012年   34篇
  2011年   27篇
  2010年   22篇
  2009年   26篇
  2008年   19篇
  2007年   21篇
  2006年   15篇
  2005年   14篇
  2004年   19篇
  2003年   12篇
  2002年   12篇
  2001年   6篇
  2000年   4篇
  1999年   3篇
  1998年   6篇
  1997年   5篇
  1996年   5篇
  1995年   3篇
  1994年   1篇
  1993年   4篇
  1992年   5篇
  1991年   2篇
  1990年   1篇
  1989年   1篇
  1988年   1篇
  1986年   1篇
排序方式: 共有459条查询结果,搜索用时 351 毫秒
21.
动力与热力抬升对烟气抬升高度的影响分析   总被引:1,自引:0,他引:1  
通过模式选择和计算,得出烟气抬升高度的增加与动能和热能的关系,表明当烟囱出口处风速分别为3 m/s、2 m/s和1 m/s时欲增加同样大小的烟气抬升高度,需要的动能比热能要高,结论认为烟气的热力提升比动力提升的贡献大。  相似文献   
22.
Fenton氧化在废水处理中的应用   总被引:2,自引:0,他引:2  
综述了近年来Fenton氧化在废水处理领域的应用状况,对Fenton试剂氧化的机理和主要影响因素:温度、pH、反应时间、H2O2和Fe2+的投加量、H2O2/Fe2+量比以及反应动力学模型进行了简要介绍.最后探讨了Fenton氧化技术在废水处理领域现存不足之处及今后的发展趋势.  相似文献   
23.
Dissipation of chlorpyrifos in pakchoi-vegetated soil in a greenhouse   总被引:2,自引:1,他引:1  
The dissipation of chlorpyrifos in pakchoi-vegetated soil was investigated in the summer and autumn in a greenhouse and field, respectively. The dissipation of chlorpyrifos in pakchoi-grown soil was comparatively described by fitting the residue data to seven models (lst-order, 1.5th-order, 2nd-order, RF lst-order, RF 1.5th-order, RF 2nd-order, and bi-exponential or two-compartment models). Statistical analysis was performed using the SPSS 11.5 statistical package. The bi-exponential model was selected as the optimal model according to the coefficient of determination r^2. The dissipation half-lives (DT50) of chlorpyrifos in pakchoi-vegetated soil at the recommended dose in the summer and autumn, calculated by the bi-exponential model, were 0.6 and 1.2 d in a greenhouse, 0.4 and 1.0 d in a field, respectively; the corresponding values at double dose were 1.2 and 2.1 d in a greenhouse, 0.5 and 1.3 d in a field, respectively. The kinetic data indicate the dissipation of chlorpyrifos in pakchoi-grown soil in a greenhouse is slower than that in a field, and dissipates slower in the autumn than in the summer.  相似文献   
24.
为研究燃料氢气泄漏、爆炸的特性和规律,预防高压储氢系统中氢气泄漏爆炸事故发生,以加氢站为背景,数值仿真45 MPa高压储罐氢气泄漏并引发爆炸事故,分析泄漏爆炸动力学性质以及爆炸波在非均匀氢气浓度中的传播机制。同时,基于泄漏爆炸事故演化的力学机理,开展氢气泄漏爆炸动态风险分析,针对氢气不同泄漏量,建立泄漏扩散形成的气云体积、气云爆炸产生的冲击波与空间x,z方向上危害距离之间关系。研究结果表明:氢气泄漏过程中,气云氢气浓度变化与流场雷诺数具有较好一致性;氢气扩散受到高压储氢罐周围装置影响,流场中氢气浓度分布不均匀;当发生燃烧爆炸事故时,冲击波参数和湍动能变化梯度大;得到复杂布局区域冲击波超压峰值与比例距离之间关系式,其相比于理论方法更精细、计算结果更准确。研究结果可为降低高压储氢系统泄漏爆炸事故后果、采取有效防护措施提供一定依据。  相似文献   
25.
利用热重分析(TGA)研究船舶塑料垃圾在不同升温速率和不同气氛下的热解特性,并得到了热解动力学参数。结果表明,船舶塑料垃圾的热解过程主要有3个阶段,比一般塑料热解复杂;随着升温速率增大,最大热解速率和最大热解速率温度等热解特性参数也增大,反应变得更剧烈;N2/CO2比为4∶1时,热解反应进行得最完全,固体残留率最少。动力学分析表明,采用3个连续一级反应模型能很好地拟合实验数据;不同的升温速率和气氛比对反应各阶段活化能均有不同程度的影响。  相似文献   
26.
表面活性剂改性4A分子筛对Cr(VI)的吸附行为   总被引:1,自引:0,他引:1  
采用浸渍法对4A分子筛进行表面改性,通过引入阳离子表面活性剂,使4A分子筛表面附着季铵型阳离子,并与反离子Br-形成"阴离子交换膜",从而促使更多的Cr(VI)阴离子通过离子交换吸附到改性4A分子筛上,通过X-射线衍射(XRD)和傅里叶变换红外光谱(FTIR)对样品的物相结构和组成进行表征分析。研究表明,表面活性剂的类型和疏水碳氢链结构会影响4A分子筛的吸附能力,十八烷基三甲基溴化铵(OTAB)碳氢链长,在分子筛表面形成的双分子层密,对Cr(VI)的吸附量最大。采用准一级、准二级、Elovich和Bangham动力学模型对六价铬的吸附数据进行拟合,其中准一级动力学方程最符合十八烷基三甲基溴化铵改性分子筛的吸附行为。同时,分别从Langmuir和Redlich-Peterson等温吸附模型获得六价铬的最大吸附量为13.98 mg/g,且改性分子筛以均一表面吸附为主。  相似文献   
27.
A study was carried out in order to compare the environmental performance of two different types of adsorbents in removing arsenic (As) from wastewater. A FeCl3-based adsorbent and a poly-Fe-based adsorbent were first synthesized and their abilities in adsorbing As from wastewater were investigated in terms of the adsorption density and the rate of adsorption. Here, it should be noted that the main material being used in the synthesis of the poly-Fe-based adsorbent was a waste product, known as polyferric sulfate or poly-Fe in short, which exits the manufacturing process of titanium dioxide.Both adsorbents were then compared in the context of life-cycle assessment (LCA). In other words, the experimental results (i.e. the value of the adsorption density and the rate of adsorption) were input into the LCA model in order to assess the environmental performance of each adsorbent in removing arsenic. An estimate for the environmental burden of each option was finally calculated as the sum of the depletion of abiotic resources (ADP), the global warming potential (GWP), the acidification potential (AP), the photo-oxidant formation potential (POCP), the eutrophication potential (EP), and the human toxicity potential (HTP). The main finding of this study was that the adsorption of arsenic by using the poly-Fe-based adsorbent is more attractive treatment option in the environmental protection point of view than the adsorption by using the FeCl3-based adsorbent, which generates a relatively larger environmental burden.  相似文献   
28.
The objective of this study was to quantify 2,4-D (2,4-dichlorophenoxyacetic acid) mineralization in soil profiles characteristic of hummocky, calcareous-soil landscapes in western Canada. Twenty-five soil cores (8 cm inner diameter, 50 to 125 cm length) were collected along a 360 m transect running west to east in an agricultural field and then segmented by soil-landscape position (upper slopes, mid slopes, lower slopes and depressions) and soil horizon (A, B, and C horizons). In the A horizon, 2,4-D mineralization commenced instantaneously and the mineralization rate followed first-order kinetics. In both the B and C horizons, 2,4-D mineralization only commenced after a lag period of typically 5 to 7 days and the mineralization rate was biphasic. In the A horizon, 2,4-D mineralization parameters including the first-order mineralization rate constant (k 1), the growth-linked mineralization rate constant (k 2) and total 2,4-D mineralization at the end of the experiment at 56 days, were most strongly correlated to parameters describing 2,4-D sorption by soil, but were also adequately correlated to soil organic carbon content, soil pH, and carbonate content. In both B and C horizons, there was no significant correlation between 2,4-D mineralization and 2,4-D sorption parameters, and the correlation between soil properties and 2,4-D mineralization parameters was very poor. The k 1 significantly decreased in sequence of A horizon (0.113% day?1) > B horizon (0.024% day?1) = C horizon (0.026% day?1) and in each soil horizon was greater than k 2. Total 2,4-D mineralization at 56 days also significantly decreased in sequence of A horizon (42%) > B horizon (31%) = C horizon (27%). In the A horizon, slope position had little influence on k 1 or k 2, except that k 1 was significantly greater in upper slopes (0.170% day?1) than in lower slopes (0.080% day?1). Neither k 1 nor k 2 was significantly influenced by slope position in the B or C horizons. Total 2,4-D mineralization at 56 days was not influenced by slope positions in any horizon. Our results suggest that, when predicting 2,4-D transport at the field scale, pesticide fate models should consider the strong differences in 2,4-D mineralization between surface and subsurface horizons. This suggests that 2,4-D mineralization is best predicted using a model that has the ability to describe a range of non-linear mineralization curves. We also conclude that the horizontal variations in 2,4-D mineralization at the field scale will be difficult to consider in predictions of 2,4-D transport at the field scale because, within each horizon, 2,4-D mineralization was highly variable across the twenty-five soil cores, and this variability was poorly correlated to soil properties or soil-landscape position.  相似文献   
29.
Fenton法处理垃圾渗滤液的参数优化及反应动力学模型   总被引:1,自引:0,他引:1  
采用Fenton法处理垃圾渗滤液,研究反应时间、初始浓度、pH、Fenton试剂用量对垃圾渗滤液TOC去除率的影响。研究结果表明,最优反应条件是反应时间30 min,初始pH为3.0,初始[H2O2]0=7 310 mg/L,最佳[H2O2]/[Fe2+]摩尔比为5,反应温度为室温,此时渗滤液的TOC去除率达到70.3%。渗滤液矿化过程符合一级反应动力学,并建立了符合该渗滤液的反应动力学模型。  相似文献   
30.
La在模拟水生态系统中的动力学行为   总被引:2,自引:0,他引:2  
采用140La放射示踪技术,研究了稀土元素镧(La)在模拟水生态系统各组分中的迁移分布规律.并建立了相应的数学模型.结果表明,La在模拟水生态系统各组分中的积累率大小依次为:金鱼藻>底泥>螺蛳>鱼,La在系统内的动态变化规律可用封闭分室模型来描述.  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