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391.
采用高斯点源模型对建陶生产造成的SO2地面浓度增量进行计算.利用比例下降模型计算建陶业的SO2允许排放总量,并根据企业的设备生产能力进行了总量分配,在方法上具有较强的可操作性,计算结果表明,可有效降低所在地区的SO2地面浓度.  相似文献   
392.
A two-dimensional (2D) laboratory model was used to study effects of gravity on areal recovery of a representative dense non-aqueous phase liquid (DNAPL) contaminant by an alcohol pre-flood and co-solvent flood in dipping aquifers. Recent studies have demonstrated that injection of alcohol and co-solvent solutions can be used to reduce in-situ the density of DNAPL globules and displace the contaminant from the source zone. However, contact with aqueous alcohol reduces interfacial tension and causes DNAPL swelling, thus facilitating risk of uncontrolled downward DNAPL migration. The 2D laboratory model was operated with constant background gradient flow and a DNAPL spill was simulated using tetrachloroethene (PCE). The spill was dispersed to a trapped, immobile PCE saturation by a water flood. Areal PCE recovery was studied using a double-triangle well pattern to simulate a remediation scheme consisting of an alcohol pre-flood using aqueous isobutanol ( approximately 10% vol.) followed by a co-solvent flood using a solution of ethylene glycol (65%) and 1-propanol (35%). Experiments were conducted with the 2D model oriented in the horizontal plane and compared to experiments at the 15 degrees and 30 degrees dip-angle orientations. Injection was applied either in the downward or upward direction of flow. Experimental results were compared to theoretical predictions for flood front stability and used to evaluate effects of gravity on areal PCE recovery. Sensitivity experiments were performed to evaluate effects of the alcohol pre-flood on PCE areal recovery. For experiments conducted with the alcohol pre-flood and the 2D model oriented in the horizontal plane, results indicate that 89-93% of source zone PCE was recovered. With injection oriented downward, results indicate that areal PCE recovery was 70-77% for a 15 degrees dip angle and 57-59% for a 30 degrees dip angle. With injection oriented upward, results indicate that areal PCE recovery was 57-60% at the 30 degrees dip angle, which was similar to PCE recovery for injection in the downward flow direction. Lower areal PCE recovery at greater dip angles in either direction of flow was attributed to DNAPL swelling and migration, flood front instabilities and bypassing of the displaced fluid past the extraction wells during the alcohol pre-flood. Additional results demonstrate that the use of an alcohol pre-flood can be beneficial in improving DNAPL recovery in the horizontal orientation, but pre-flooding may reduce areal recovery efficiency in dip-angle orientations. This study also demonstrates the use of theoretical perturbation (fingering) analysis in predicting NAPL recovery efficiency for flooding processes in remediating aquifers with dip angles.  相似文献   
393.
Shon ZH  Kim KH 《Chemosphere》2006,63(11):1859-1869
This study examines the oxidation of reduced sulfur compounds (RSCs) in urban ambient air. The photochemical conversions of RSC (such as DMS, CS2, H2S, DMDS, and CH3SH) to a further oxidized form (e.g., SO2, MSA, and H2SO4) were assessed using a photochemical box model. For our model simulation of RSC oxidation, measurements were taken at an urban monitoring station in Seoul, Korea (37.6° N, 127° E) during three separate time periods (e.g., Sept. 17–18, Oct. 23, and Oct. 27–28, 2003). The results indicate that DMS and H2S were the dominant RSCs with concentrations of 370 ± 140 and 110 ± 60 pptv, respectively. The photochemical conversion of DMDS to SO2 was found to occur more efficiently than other RSCs. The overall results of our study suggest that photochemical conversion of RSCs accounted for less than 15% of the observed SO2 during the measurement period. The SO2 production from DMS oxidation (mainly by the reaction with OH) was found to be affected primarily by the abstraction channel due to high NOx levels during the experimental conditions.  相似文献   
394.
为了解决常规污水处理技术无法进行完整的硝化反硝化过程,污水厂出水中氨氮、总氮、总磷偏高以及运行成本较高的问题,以某污水厂排水为研究对象,通过物化与生化耦合,构建化学催化生物耦合床(CCBF)脱氮系统,研究CCBF系统对污水厂排水中氨氮、总氮、总磷和COD的去除效能。结果表明:当DO为5.5~6.0 mg·L−1、RT为8 h、C/N为1.5∶1时,CCBF可将${\rm{NH}}_4^{+} $-N从48.5 mg·L−1降至4.58 mg·L−1、TN从51.2 mg·L−1降至6.5 mg·L−1、TP从6.6 mg·L−1降至0.48 mg·L−1、COD从78.5 mg·L−1降至33 mg·L−1,去除率分别达到89.5%、85.7%、92.5%和57.9%;污水经处理后,氨氮、总氮、总磷、COD均达到城镇污水处理厂污染物排放标准(GB 18918-2002)一级A排放标准。利用Eckenfelder方程对系统脱氮过程进行模拟,求得${n_{{\rm{NH}}_4^ +{\text{-}} {\rm{N}}}} $=0.314 76,nTN=0.282 21,${K_{{\rm{NH}}_4^ +{\text{-}} {\rm{N}}}} $=0.128 02,KTN=0.218 59,与水力负荷为0.000 8~0.007 m3·(m2·min)−1的常规生物处理相比,系统内部生物量充足、活性高,物化与生物耦合强化效果明显。  相似文献   
395.
为了解煤胶体对汞的吸附动力学特性,采用沉降法和离心法提取由霍林河采集煤样中的煤胶体(0~2、2~5、5~10 μm),采用批量实验对不同粒径和不同温度下,煤胶体对汞的吸附动力学特性进行了研究。结果表明:煤胶体对汞的吸附反应为吸热反应,以化学吸附为主,其吸附动力学过程可用准二级动力学方程和双室模型很好的描述。煤胶体对汞的平衡吸附量随粒径的减小和温度的升高而逐渐增大,不同粒径煤胶体受温度影响的大小关系为(5~10)μm > (2~5)μm > (0~2)μm。煤胶体对汞的吸附从初始阶段到达到表观平衡,快速吸附均占据优势。在表观平衡时,粒径越大,快速吸附的贡献率越小。煤胶体对汞的吸附反应速率随温度升高和粒径减小而增大。温度越高、粒径越小,快速吸附速率越大;而慢速吸附速率则随温度升高和粒径增大而增大。汞在0~2 μm和2~5 μm煤胶体上的吸附过程,粒内扩散是其主要控速步骤;而对于5~10 μm的煤胶体,膜扩散是主要控速步骤。  相似文献   
396.
Numerical simulations of colloid transport in discretely fractured porous media were performed to investigate the importance of matrix diffusion of colloids as well as the filtration and remobilization of colloidal particles in both the fractures and porous matrix. To achieve this objective a finite element numerical code entitled COLDIFF was developed. The processes that COLDIFF takes into account include advective-dispersive transport of colloids, filtration and remobilization of colloidal particles in both fractures and porous matrix, and diffusive interactions of colloids between the fractures and porous matrix. Three sets of simulations were conducted to examine the importance of parameters and processes controlling colloid migration. First, a sensitivity analysis was performed using a porous block containing a single fracture to determine the relative importance of various phenomenological coefficients on colloid transport. The primary result of the analysis showed that the porosity of the matrix and the process of colloid filtration in fractures play important roles in controlling colloid migration. Second, simulations were performed to replicate and examine the results of a laboratory column study using a fractured shale saprolite. Results of this analysis showed that the filtration of colloidal particles in the porous matrix can greatly affect the tailing of colloid concentrations after the colloid source was removed. Finally, field-scale simulations were performed to examine the effect of matrix porosity, fracture filtration and fracture remobilization on long-term colloid concentration and migration distance. The field scale simulations indicated that matrix diffusion and fracture filtration can significantly reduce colloid migration distance. Results of all three analyses indicated that in environments where porosity is relatively high and colloidal particles are small enough to diffuse out of fractures, the characteristics of the porous matrix that affect colloid transport become more important than those of the fracture network. Because the properties of the fracture network tend to have greater uncertainty due to difficulties in their measurement relative to those of the porous matrix, prediction uncertainties associated with colloid transport in discretely fractured porous media may be reduced.  相似文献   
397.
推导了BAF前置反硝化工艺简化动力学模型,揭示了BAF去除有机物与反应速率常数与膜厚的关系。同时以生物膜中活性物质与非活性物质增长生物数学模型体系为基础,从理论上推导了BAF最佳膜厚的范围。  相似文献   
398.
综合交通枢纽运营安全集成管理机制的构建   总被引:2,自引:0,他引:2  
为提高综合交通枢纽(ITH)运营安全管理的效率和效果,从脆弱性的角度,分析综合交通枢纽运营安全事故的机理和运营安全管理的特性,构建综合交通枢纽运营安全集成管理机制。该机制以安全信息、安全组织和安全资源的协调、集成和优化为核心,包含干扰监测、威胁预警、漏洞修复、事故控制、鲁棒性提升和应急与恢复等实施机制。建立包含管理措施和技术手段的支撑体系。研究表明:脆弱性是综合交通枢纽运营安全事故发生的根源;该机制以脆弱性为突破口,通过若干管理措施和技术手段,能够实现综合交通枢纽运营安全的全要素、全过程和全资源的集成管理。  相似文献   
399.
基于化工园区整体风险量分析的安全规划研究   总被引:1,自引:2,他引:1  
通过对园区安全容量和危险量的分析,得到园区整体的风险评估值;提出并定义园区危安比最大临界点,用其反映园区的最大可接受风险量;运用"二八法则",确定危安比上限;当危安比在3种不同值域区间下,对应的园区安全规划的重点不同;从园区整个生命周期考虑,提出包含各个阶段的园区安全规划主要内容。  相似文献   
400.
用2,3-二羟基苯甲酸经羟基保护、酰胺化、酯化和去保护4步反应,生成一种新型的四齿丙二酸二(2-(2,3-二羟基苯甲酰胺)乙基)酯配体.采用傅里叶变换红外光谱(FT-IR)、紫外-可见光谱(UV-Vis)、核磁共振氢谱(1H NMR)、核磁共振碳谱(13C NMR)和质谱(MS)对其结构进行了表征.在中性pH值条件下,研究了这种配体对铀酰离子的络合能力.结果表明,丙二酸二(2-(2,3-二羟基苯甲酰胺)乙基)酯配体与铀酰离子的螯合常数为23.2.  相似文献   
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