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481.
稀土金属具有一些特殊的性能,这使得其对碳质材料还原NO的反应可能表现出特殊的催化效果,而此方面的研究没有报道.为了研究稀土金属对活性炭还原NO反应的催化效果,采用浸渍法制备了负载氧化镧的活性炭颗粒(La/C),并在无氧的固定床反应器中进行了程序升温反应和等温反应,考察了气体流量、NO的入口浓度、反应温度和氧化镧负载量对反应活性的影响,同时对反应机理和动力学进行了初步探讨.研究结果表明负载氧化镧的活性炭还原NO的反应是一级反应.由于炭表面3%(质量分数)的氧化镧的存在,C-NO反应的起始反应温度从500 ℃降低到300 ℃,反应活性大大提高,反应活化能从88.95 kJ/mol降低到51.05 kJ/mol.氧化镧的负载量对反应活性有重要影响,但负载量的大量增加对反应活性的提高效果甚微,最佳负载量为1.5%.La/C体系在反应中较稳定,而反应温度的升高对其稳定性不利. 相似文献
482.
Influence of hydrogeochemical processes on zero-valent iron reactive barrier performance: a field investigation 总被引:1,自引:0,他引:1
Geochemical and mineralogical changes were evaluated at a field Fe0-PRB at the Oak Ridge Y-12 site concerning operation performance during the treatment of U in high NO3- groundwater. In the 5-year study period, the Fe0 remained reactive as shown in pore-water monitoring data, where increases in pH and the removal of certain ionic species persisted. However, coring revealed varying degrees of cementation. After 3.8-year treatment, porosity reduction of up to 41.7% was obtained from mineralogical analysis on core samples collected at the upgradient gravel-Fe0 interface. Elsewhere, Fe0 filings were loose with some cementation. Fe0 corrosion and pore volume reduction at this site are more severe due to the presence of NO3- at a high level. Tracer tests indicate that hydraulic performance deteriorated: the flow distribution was heterogeneous and under the influence of interfacial cementation a large portion of water was diverted around the Fe0 and transported outside the PRB. Based on the equilibrium reductions of NO3- and SO4(2-) by Fe0 and mineral precipitation, geochemical modeling predicted a maximum of 49% porosity loss for 5 years of operation. Additionally, modeling showed a spatial distribution of mineral precipitate volumes, with the maximum advancing from the interface toward downgradient with time. This study suggests that water quality monitoring, coupled with hydraulic monitoring and geochemical modeling, can provide a low-cost method for assessing PRB performance. 相似文献
483.
利用铁屑微电解-共沉淀法处理屠宰场废水,介绍其作用机理,考察了废水pH值、铁屑用量、反应时间、曝气时间和操作方式等因素对色度和CODCr去除率的影响.结果表明,在废水pH值为4,铁屑用量为15%,常温反应4 h,曝气时间2 h条件下,色度去除率可达100%,CODCr去除率达92.68%. 相似文献
484.
介绍了氧化铁黄生产中的废水治理情况,同时其产生的废渣可回收利用。经过治理产生的环境、经济和社会效益显著。 相似文献
485.
光助Fenton氧化、化学絮凝法联合处理R盐废水的研究 总被引:4,自引:0,他引:4
采用光助Fenton氧化、化学絮凝法联合处理生物难降解的R盐废水,考察了不同反应条件对处理效果的影响.试验结果表明,光助Fenton氧化、化学絮凝法联合处理废水,两者之间存在协同作用,可以提高处理效果,降低处理成本.在最佳试验条件下,R盐废水经光助Fenton氧化、化学絮凝法联合处理后,COD去除率可达90%以上. 相似文献
486.
487.
基于常熟河网原型调水实验和水功能区划,建立了感潮地区河网水量水质模型,对常熟河道水质降解系数及水环境容量进行了计算,并按照点源和面源对区域内污染源进行统计,在此基础上进行了常熟河网水污染物总量控制值和现状削减量的计算,为该地区的水污染防控提供了科学依据。 相似文献
488.
A Triassic sandstone aquifer polluted with a mixture of phenolic hydrocarbons has been investigated by means of high-resolution groundwater sampling. Samples taken at depth intervals of 1 m have revealed the presence of a diving pollutant plume with a sharply defined upper margin. Concentrations of pollutant phenols exceed 4 g/l in the plume core, rendering it sterile but towards the diluted upper margin evidence for bacterial sulphate reduction (BSR) has been obtained. Groundwaters have been analysed for both delta34S-SO4 and delta18O-SO4. Two reservoirs have been identified with distinct sulphate oxygen isotope ratios. Groundwater sulphate (delta18O-SO4 = 3-5/1000) outside the plume shows a simple linear mixing trend with an isotopically uniform pollutant sulphate reservoir (delta18O-SO4 = 10-12/1000) across the plume margin. The sulphur isotope ratios do not always obey a simple mixing relation, however, at one multilevel borehole, enrichment in 34SO4 at the plume margin is inversely correlated with sulphate concentration. This and the presence of 34S-depleted dissolved sulphide indicate that enrichment in 34SO4 is the result of bacterial sulphate reduction. Delta34S analysis of trace hydrogen sulphide within the plume yielded an isotope enrichment factor (epsilon) of -9.4/1000 for present-day bacterial sulphate reduction. This value agrees with a long-term estimate (-9.9/1000) obtained from a Rayleigh model of the sulphate reduction process. The model was also used to obtain an estimate of the pre-reduction sulphate concentration profile with depth. The difference between this and the present-day profiles then gave a mass balance for sulphate consumption. The organic carbon mineralisation that would account for this sulphate loss is shown to represent only 0.1/1000 of the phenol concentration in this region of the plume. Hence, the contribution of bacterial sulphate reduction to biodegradation has thus far been small. The highest total phenolic concentration (TPC) at which there is sulphur isotope evidence of bacterial sulphate reduction is 2000 mg/l. We suggest that above this concentration, the bactericidal properties of phenol render sulphate-reducing bacteria inactive. Dissolved sulphate trapped in the concentrated plume core will only be utilised by sulphate reducers when toxic phenols in the plume are diluted by dispersion during migration. 相似文献
489.
490.
Dale R. Van Stempvoort James Armstrong Bernhard Mayer 《Journal of contaminant hydrology》2007,92(3-4):184-207
Despite a rapid expansion over the past decade in the reliance on intrinsic bioremediation to remediate petroleum hydrocarbon plumes in groundwater, significant research gaps remain. Although it has been demonstrated that bacterial sulfate reduction can be a key electron accepting process in many petroleum plumes, little is known about the rate of this reduction process in plumes derived from crude oil and gas condensates at cold-climate sites (mean temperature <10 degrees C), and in complex hydrogeological settings such as silt/clay aquitards. In this field study, sulfate was injected into groundwater contaminated by gas condensate plumes at two petroleum sites in Alberta, Canada to enhance in-situ bioremediation. In both cases the groundwater near the water table had low temperature (6-9 degrees C). Monitoring data had provided strong evidence that bacterial sulfate reduction was a key terminal electron accepting process (TEAP) in the natural attenuation of dissolved hydrocarbons at these sites. At each site, water with approximately 2000 mg/L sulfate and a bromide tracer was injected into a low-sulfate zone within a condensate-contaminant plume. Monitoring data collected over several months yielded conservative estimates for sulfate reduction rates based on zero-order kinetics (4-6 mg/L per day) or first-order kinetics (0.003 and 0.01 day(-1)). These results favor the applicability of in-situ bioremediation techniques in this region, under natural conditions or with enhancement via sulfate injection. 相似文献