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901.
Regional Environmental Change - Most studies of major disasters focus on the impacts of the event and the short-term responses. Some evaluate the underlying causes of vulnerability, but few...  相似文献   
902.
The first objective of this study was to provide data of arsenic (As) levels in Peninsular Malaysia based on soil samples and accumulation of As in Centella asiatica collected from 12 sampling sites in Peninsular Malaysia. The second objective was to assess the accumulation of As in transplanted C. asiatica between control and semi-polluted or polluted sites. Four sites were selected which were UPM (clean site), Balakong (semi-polluted site), Seri Kembangan (semi-polluted site) and Juru (polluted site). The As concentrations of plant and soil samples were determined by Instrumental Neutron Activation Analysis. The As levels ranged from 9.38 to 57.05 μg/g dw in soils, 0.21 to 4.33 μg/g dw in leaves, 0.18 to 1.83 μg/g dw in stems and 1.32–20.76 μg/g dw in roots. All sampling sites had As levels exceeding the CCME guideline (12 μg/g dw) except for Kelantan, P. Pauh, and Senawang with P. Klang having the highest As in soil (57.05 μg/g dw). In C. asiatica, As accumulation was highest in roots followed by leaves and stems. When the As level in soils were higher, the uptake of As in plants would also be increased. After the transplantation of plants to semi-polluted and polluted sites for 3 weeks, all concentration factors were greater than 50 % of the initial As level. The elimination factor was around 39 % when the plants were transplanted back to the clean sites for 3 weeks. The findings of the present study indicated that the leaves, stems and roots of C. asiatica are ideal biomonitors of As contamination. The present data results the most comprehensive data obtained on As levels in Malaysia.  相似文献   
903.
Atmospheric corrections for multi-temporal optical satellite images are necessary, especially in change detection analyses, such as normalized difference vegetation index (NDVI) rationing. Abrupt change detection analysis using remote-sensing techniques requires radiometric congruity and atmospheric correction to monitor terrestrial surfaces over time. Two atmospheric correction methods were used for this study: relative radiometric normalization and the simplified method for atmospheric correction (SMAC) in the solar spectrum. A multi-temporal data set consisting of two sets of Landsat images from the period between 1991 and 2002 of Penang Island, Malaysia, was used to compare NDVI maps, which were generated using the proposed atmospheric correction methods. Land surface temperature (LST) was retrieved using ATCOR3_T in PCI Geomatica 10.1 image processing software. Linear regression analysis was utilized to analyze the relationship between NDVI and LST. This study reveals that both of the proposed atmospheric correction methods yielded high accuracy through examination of the linear correlation coefficients. To check for the accuracy of the equation obtained through linear regression analysis for every single satellite image, 20 points were randomly chosen. The results showed that the SMAC method yielded a constant value (in terms of error) to predict the NDVI value from linear regression analysis-derived equation. The errors (average) from both proposed atmospheric correction methods were less than 10%.  相似文献   
904.
膜法水处理技术的研究与应用现状   总被引:2,自引:1,他引:1  
介绍了膜法水处理技术的发展历程,其应用和研究现状,对超滤、微滤、纳滤、反渗透、电渗析、渗透蒸发、液膜技术等在给水处理,废水处理方面的应用作了较全面的介绍。  相似文献   
905.
Cu~(2+)改性活性炭的制备及其去除废水中CN~-的研究   总被引:1,自引:0,他引:1  
以活性炭为载体负载溶液中的 Cu~(2+),Cu~(2+)改性活性炭对溶液中 CN~-的去除效果较好。Cu~(2+)改性活性炭的最佳制备条件:活性炭加入量为1 g,质量浓度为5 g/L 的 CuSO_4溶液加入量为50 mL,溶液 pH 为4,负载时间为5.0 h。在此最佳条件下活性炭的最大 Cu~(2+)负载量为25.90 mg(以每克活性炭计)。Cu~(2+)改性后活性炭的 CN~-去除率明显提高,由22.10%提高至94.07%。Cu~(2+)改性活性炭吸附CN~-的最佳实验条件:溶液 pH 为12~13,吸附时间为9 h。Cu~(2+)改性活性炭对 CN~-的饱和吸附量为22 mg/g。Mg~(2+),K~+,Ca~(2+),Cl~-,SO_4~(2-),CO_3~(2-),AsO_3~-对 Cu~(2+)改性活性炭的 CN~-去除率基本没有影响。Cu~(2+)改性活性炭的动态吸附实验表明,开始一段时间流出液中 CN~-含量几乎为零,远低于国家排放标准(0.5 mg/L)。  相似文献   
906.
This paper presents a novel superstructure-based optimization model for the synthesis of industrial water networks with partitioning regenerators. Such regenerators function by splitting a contaminated water stream into a regenerated lean stream and a low-quality reject stream. Membrane separation-based processes are examples of these types of regenerators. The optimization model presented in this work integrates a single, centralized partitioning regenerator with a source–demand superstructure under the assumption that the processes within the plant are of the fixed flow rate type. The formulation is non-linear as a result of the presence of bilinear terms in the regenerator balance equations, but global optimal solutions can be found using commercial software. The features of the model are illustrated by solving case studies from the literature. It is notable from these examples that considerable design flexibility exists in networks of this type, since potentially both the lean and reject streams from the partitioning regenerator can be reused/recycled within the plant.  相似文献   
907.
超声破解吸持稠油粘土颗粒的研究   总被引:2,自引:0,他引:2  
在频率为28 kHz的超声辐照下,研究了超声作用功率和辐照时间对石油污染土壤淋洗液中吸持稠油粘土颗粒的破解作用,并采用GC/MS分析了超声辐照时间对淋洗液中特征有机物的影响。结果表明,随着超声作用功率和辐照时间的增加,粘土颗粒吸持的稠油显著下降,辐照时间为45 min,作用功率为100 W时,粘土颗粒吸持稠油的解吸率为7925%;作用功率为60 W,辐照时间为75 min时,粘土颗粒吸持稠油的解吸率为77.36%。超声波能够显著增加解吸稠油在水中的溶解率,辐照时间为45 min,作用功率为80 W时,水相含油率升高92%;当作用功率为60 W,辐照时间为75 min时,水相含油率升高近1倍。随着超声辐照时间的增加,极性相对较强的环烷酮类有机物的相对丰度随之增加,极性相对较弱的环烷二酮类有机物相对丰度则显著减小。超声波有利于异位化学淋洗在高含粘土颗粒石油污染土壤修复中的应用。  相似文献   
908.
石灰湿法脱硫传质-反应过程机理   总被引:3,自引:1,他引:3  
对以旋流板塔作吸收器的石灰湿法烟气脱硫技术进行了试验研究。分析了为浆液吸收SO2的传质-反应过程,并提出了Ca(OH)2浆液吸收SO2的传质-反应过程机理。本机理认为,总反应速度由气相中SO2的扩散(气相阻力)和液相中Ca(OH)2固体的溶解(包括在液相阻力之内)及扩散控制;同时认为,反应过程可分为气相阻力控制、所液共同控制、液相阻力控制3个阶段。此外,本机得到了实验的验证。以上结果将有助于改进为  相似文献   
909.
在沈阳张士灌区采用综合方法治理镉污染农田。在中度和轻度污染土壤种植水稻,控制灌溉水质(Cd~2+<2PPb,PH>7,Cl-<100ppm)或以清水灌溉,在重污染区,采用农业生态工程改良方法如农业改良(繁育水稻、玉米良种),繁育绿化苗木和草皮、种植甜高梁提取酒精。结果表明,农业生态工程方法是合理利用和改良严重镉污染农田的良好途径。  相似文献   
910.
A home-made inexpensive passive diffusion bag (PDB) sampler, prepared by filling deionized water in low-density polyethylene (LDPE) tubes, was evaluated for volatile organic compounds (VOC) sampling in groundwater at industrial contamination sites. Impacts of environmentally relevant conditions on the sampling equilibration time and partitioning of VOCs between the sampler and the water sample were investigated. Sample salinity, agitation and temperature can influence the equilibration time, but generally sampling equilibration was obtained in 14 days under real field sampling of VOCs in groundwater. Both laboratory study and field testing in a contaminated site showed that the VOC concentrations in the developed sampler were equal to those in the water samples at equitibrium. Coupled with a purge and trap concentrator-gas chromatograph-mass spectrometer (P&T-GC-MS), the developed PDB sampler provided a low-cost sampling device for routine monitoring of VOCs in groundwater in wells, with LODs in the range of 2.9-10 μg/L. The proposed PDB was applied to determine VOCs in groundwater at an industrial contamination site, and the present results agreed well with those determined using conventional pump-and-sample monitoring. All the studied 13 VOCs were tested in the four wells in the industrial contamination sites, with their concentrations in the range of 12-73660 μg/L. In addition, while benzene and toluene were heavily contaminated up to a maximum concentration of 74000 μg/L and 6000 μg/L, respectively, 1,2,3-trichlorobenzene and bromobenzene had relatively low contamination levels (below 25 μg/L).  相似文献   
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