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91.
改进型活性炭吸附法去除污水生化处理过程中的恶臭 总被引:3,自引:0,他引:3
采用二级生化处理工艺的生活污水处理系统,在运转一段时间后会产生氨气、硫化氢等有刺激性的气体,对环境造成污染。在臭气的各种处理方法中,改进型活性炭吸附法对污水生化处理过程中产生的氨气和硫化氢气体的去除有特别显著、持久的效果,有望推广应用到更多的实际处理过程。阐述了改进型活性炭吸附法的工艺、材料特点和除湿装置作用。 相似文献
92.
93.
流化吸附法净化处理沥青烟气的研究 总被引:4,自引:0,他引:4
以炉灰渣为吸附剂,在流化状态下吸附净化沥青烟气的实验室小试表明,炉灰渣的吸附容量高达185mg/g,一次性净化效率为99%。该工艺具有运转成本低.操作简单和以废治废的特点,为治理沥青烟气污染提供一条新途径。 相似文献
94.
95.
Nobuhisa Watanabe Saburo Inoue Hisao Ito 《Journal of Material Cycles and Waste Management》1999,1(1):38-47
The arsenic and antimony balance in two municipal waste incinerators was investigated. Initially, the production rates of
ash and wet scrubber effluent were estimated. Then the arsenic and antimony in the ash and wet scrubber effluent were determined,
which gave an estimate of the elemental balance. The total amounts of arsenic and antimony in the municipal waste were 0.9 g/t
and 30–44 g/t, respectively. The distributions to fly ash were 45–47% and 33–74% for arsenic and antimony, respectively. The
distribution mechanisms of arsenic and antimony are discussed from the viewpoints of their thermodynamics as well as their
initial valencies, which greatly affect their behaviour.
Received: July 2, 1998 / Accepted: February 27, 1999 相似文献
96.
活性炭吸附室内空气中挥发性有机化合物 总被引:13,自引:0,他引:13
活性炭吸附室内空气中挥发性有机化合物的10%穿透时间与气相浓度及挥发性有机化合物的种类有关,通过对苯、甲苯和丙酮的实验研究,得出了由高浓度估算室内低浓度时炭床10%穿透时间的经验公式tb,1=tb,h(C0,1/C0,h)^a,其中a值是与炭床性能及挥发性有机化合物种类有关的参数,可通过实验确定。 相似文献
97.
Immobilization of Pb(II), Cd(II) and Ni(II) ions on kaolinite and montmorillonite surfaces from aqueous medium 总被引:4,自引:0,他引:4
The present study investigates the immobilization of Pb(II), Cd(II) and Ni(II) on clays (kaolinite and montmorillonite) in aqueous medium through the process of adsorption under a set of variables (concentration of metal ion, amount of clay, pH, time and temperature of interaction). Increasing pH favours the removal of metal ions till they are precipitated as the insoluble hydroxides. The uptake is rapid with maximum adsorption being observed within 180 min for Pb(II) and Ni(II) and 240 min for Cd(II). A number of available models like the Lagergren pseudo first-order kinetics, second-order kinetics, Elovich equation, liquid film diffusion and intra-particle diffusion are utilized to evaluate the kinetics and the mechanism of the immobilization interactions. Two isotherm equations due to Langmuir and Freundlich showed good fits with the experimental data. Kaolinite and montmorillonite have considerable Langmuir monolayer capacity with respect to Pb(II), Cd(II) and Ni(II), the values being in the range of 6.8-11.5mg/g (kaolinite) and 21.1-31.1mg/g (montmorillonite). The Freundlich adsorption capacity follows a similar order. The thermodynamics of the immobilization process indicates the same to be exothermic with Pb(II) and Ni(II), but endothermic with Cd(II). The interactions with Pb(II) and Ni(II) are accompanied by decrease in entropy and Gibbs energy while the endothermic immobilization of Cd(II) is supported by an increase in entropy and an appreciable decrease in Gibbs energy. The results have established good potentiality for kaolinite and montmorillonite to remove heavy metals like Pb(II), Cd(II) and Ni(II) from aqueous medium through adsorption-mediated immobilization. 相似文献
98.
In order to measure groundwater age and design nuclear waste disposal sites, it is important to understand the sorption behavior of tritium on soils. In this study, batch tests were carried out using four soils from China: silty clays from An County and Jiangyou County in Sichuan Province, both of which could be considered candidate sites for Very Low Level Waste disposal; silty sand from Beijing; and loess from Yuci County in Shanxi Province, a typical Chinese loess region. The experimental results indicated that in these soil media, the distribution coefficient of tritium is slightly influenced by adsorption time, water/solid ratio, initial tritium specific activity, pH, and the content of humic and fulvic acids. The average distribution coefficient from all of these influencing factors was about 0.1-0.2 mL/g for the four types of soil samples. This relatively modest sorption of tritium in soils needs to be considered in fate and transport studies of tritium in the environment. 相似文献
99.
Mosaddeghi MR Mahboubi AA Zandsalimi S Unc A 《Journal of environmental management》2009,90(2):730-739
Organic wastes are considered to be a source for the potentially pathogenic microorganisms found in surface and sub-surface water resources. Following their release from the organic waste matrix, bacteria often infiltrate into soil and may be transported to significant depths contaminating aquifers. We investigated the influence of soil texture and structure and most importantly the organic waste properties on the transport and filtration coefficients of Escherichia coli and total bacteria in undisturbed soil columns. Intact soil columns (diameter 16 cm and height 25 cm) were collected from two soils: sandy clay loam (SCL) and loamy sand (LS) in Hamadan, western Iran. The cores were amended with cow manure, poultry manure and sewage sludge at a rate of 10 Mg ha(-1) (dry basis). The amended soil cores were leached at a steady-state flux of 4.8 cm h(-1) (i.e. 0.12 of saturated hydraulic conductivity of the SCL) to a total volume of up to 4 times the pore volume of the columns. The influent (C(0)) and effluent (C) were sampled at similar time intervals during the experiments and bacterial concentrations were measured by the plate count method. Cumulative numbers of the leached bacteria, filtration coefficient (lambda(f)), and relative adsorption index (S(R)) were calculated. The preferential pathways and stable structure of the SCL facilitated the rapid transport and early appearance of the bacteria in the effluent. The LS filtered more bacteria when compared with the SCL. The effluent contamination of poultry manure-treated columns was greater than the cow manure- and sewage sludge-treated ones. The difference between cow manure and sewage sludge was negligible. The lambda(f) and S(R) values for E. coli and total bacteria were greater in the LS than in the SCL. This indicates a predominant role for the physical pore-obstruction filtration mechanisms as present in the poorly structured LS vs. the retention at adsorptive sites (chemical filtration) more likely in the better structured SCL. While the results confirmed the significant role of soil structure and preferential (macroporous) pathways, manure type was proven to have a major role in determining the maximum penetration risk of bacteria by governing filtration of bacteria. Thus while the numbers of bacteria in waste may be of significance for shallow aquifers, the type of waste may determine the risk for microbial contamination of deep aquifers. 相似文献
100.
Adsorption of phenol and its derivatives from water using synthetic resins and low-cost natural adsorbents: a review 总被引:1,自引:0,他引:1
In this article, the technical feasibility of the use of activated carbon, synthetic resins, and various low-cost natural adsorbents for the removal of phenol and its derivatives from contaminated water has been reviewed. Instead of using commercial activated carbon and synthetic resins, researchers have worked on inexpensive materials such as coal fly ash, sludge, biomass, zeolites, and other adsorbents, which have high adsorption capacity and are locally available. The comparison of their removal performance with that of activated carbon and synthetic resins is presented in this study. From our survey of about 100 papers, low-cost adsorbents have demonstrated outstanding removal capabilities for phenol and its derivatives compared to activated carbons. Adsorbents that stand out for high adsorption capacities are coal-reject, residual coal treated with H3PO4, dried activated sludge, red mud, and cetyltrimethylammonium bromide-modified montmorillonite. Of these synthetic resins, HiSiv 1000 and IRA-420 display high adsorption capacity of phenol and XAD-4 has good adsorption capability for 2-nitrophenol. These polymeric adsorbents are suitable for industrial effluents containing phenol and its derivatives as mentioned previously. It should be noted that the adsorption capacities of the adsorbents presented here vary significantly depending on the characteristics of the individual adsorbent, the extent of chemical modifications, and the concentrations of solutes. 相似文献