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681.
膜生物反应器内污泥增长规律的研究 总被引:1,自引:0,他引:1
研究了不同进水有机物浓度下MBR反应器的污泥增长和活性变化的规律,并确定了本系统三个运行阶段活性污泥增长的动力学系数(Yg和ms)。结果表明,MBR长时间不排泥和低负荷的运行方式会使污泥的活性下降和微生物种群的改变,在低负荷下运行时会出现污泥的负增长。根据经典的微生物能量代谢理论并结合各个运行阶段污泥浓度的变化情况计算得到进水COD300、180和120mg/L下MBR的Yg和ms的值,分别为0.42、0.39、0.24(gVSSgCOD^-1)和0.11、0.06、0.08(gCODgVSS^-1day^-1)。 相似文献
682.
Abstract Despite its strong advantages in resource, technology and human resource, China's Northeast Industrial Area is also experiencing problems of unreasonable industrial structure, environmental pollution, and the degradation of ecological condition, etc., which prevent this area from achieving a sustainable development. Through analyzing the resource problem, the present paper proposed a strategy of circular economy for the prosperity of this are, discussed the theories of circular economy and resource recycling, and finally concluded that improving resource productivity is at the core of circular economy. 相似文献
683.
Zhu Qirong 《中国人口.资源与环境(英文版)》2013,11(3):86-96
Abstract In this paper, using the input-output model, the author first calculated the CO2 emissions embodied in exports of China in 2002 and 2007. Then, the author empirically analyzed problems existing in the composition of exported products and analyzed its possible reasons. The research results of this paper are as follows: Since China’s entry into WTO, the CO2 emissions embodied in exports of China have been increasing rapidly; the value of exported products of high-carbon emissions industries accounts for a relatively higher proportion to China’s total exports value because China’s carbon intensive products have a certain competitive advantage. Additionally, this paper has put forward relevant suggestions based on these results. 相似文献
684.
685.
Soybean [ (L.) Merr.] stalk-based carbons were prepared by phosphoric acid activation at different carbonization temperatures. Characteristics of the prepared carbon, including specific surface area, iodine number, and amount of methylene blue sorption, were determined. Experiments on phenanthrene, naphthalene, and acenaphthene, as representatives of polycyclic aromatic hydrocarbons (PAHs), removal from aqueous solution by the prepared carbon were conducted at different levels of carbon addition. The results indicated that the specific surface area, iodine number, and amount of methylene blue sorption increased with an increase of carbonization temperature. The maximum values were observed at 700°C and were 287.63 m g, 508.99 mg g, and 90.14 mg g, respectively. The removal efficiencies of phenanthrene, naphthalene, and acenaphthene tended to increase with increasing carbon amounts and carbonization temperature. The optimal removal performance was obtained under the experimental conditions of carbon concentrations of 0.04 g 32 mL and carbonization temperature of 700°C, and the removal efficiencies of phenanthrene, naphthalene, and acenaphthene were 99.89, 100, and 95.64%, respectively. The performance of the prepared carbon was superior to that of commercial activated carbon. Additionally, for the same carbon concentrations, the removal efficiency of PAHs on prepared carbons followed the order: phenanthrene > naphthalene > acenaphthene. Results obtained from this work provide some insight into the reuse of an agricultural residue, and also provide a new application for the treatment of PAHs in contaminated water utilizing activated carbon prepared from agricultural residues. 相似文献
686.
The recovery of waste substances is important not only for the prevention of environmental issues, but also for the rational utilization of natural resources. Hydrolysis reaction in sub-critical water is a promising method for the treatment of organic wastes and has been attracting worldwide attention. In this paper, sub-critical water hydrolysis was employed as a method for producing amino acids, reducing sugars, bio-oil and gas fuels from biomass wastes. The current statuses of these useful chemicals production from biomass wastes by hydrolysis in sub-critical water were reviewed. The review indicates that sub-critical water hydrolysis can be an efficient process for recovering useful chemicals from biomass wastes. This method is renewable, sustainable, efficient, and safe for the environment. 相似文献
687.
688.
Eight heavy metals (Cu, Zn, Fe, Mn, Cd, Cr, Ni, and Pb) in 14 different wild-growing edible mushroom species (Coprinus comatus, Voluariella volvacea, Pleurotus nebrodensis, Hypsizigus marmoreus, Hericium erinaceus, Agrocybe aegerita, Lenfinus edodes, Collybia velutipes, Agaricus bisporus, Russula albida, Clitocybe conglobata, Pleurotus eryngii, Lepista sordida, and Pleurotus ostreatus) collected from Yunnan province, China, were determined by inductively coupled plasma-atomic emission spectrometry after microwave digestion. All element concentrations were determined on a dry weight basis. The ranges of element concentrations for copper, zinc, iron, manganese, cadmium, chromium, nickel, and lead were 6.8-31.9, 42.9-94.3, 67.5-843, 13.5-113, 0.06-0.58, 10.7-42.7, 0.76-5.1, and 0.67-12.9 mg/kg, respectively. In general, iron content was higher than other metals in all mushroom species. The levels of zinc, cadmium, and lead in some edible mushroom samples were found to be higher than legal limits. The relative standard deviations were found below 10%. The accuracy of procedure was confirmed by certified reference material. 相似文献
689.
Persulfate can efficiently decolorize azo dyes through oxidizing these compounds, which enabled us to develop a method of rapid spectrophotometric determination of persulfate for monitoring the wastewater treatment on the basis of the oxidation decolorization of azo dyes. Four azo dyes with different molecular structures were investigated as probes, and the influences of operation parameters including reaction time, solution pH, initial dye concentration, and initial concentration of activator Fe(2+) were checked on the determination of persulfate. Under optimum conditions, the decolorization degree of the dyes responded linearly with persulfate concentration for all the four azo dyes, and the linear range and detection limit were found to be 2.0-150 μmol L(-1) and 0.62 μmol L(-1) for rhodamine B, 2.0-100 μmol L(-1) and 0.42 μmol L(-1) for methylene blue, 4.0-150 μmol L(-1) and 0.50 μmol L(-1) for methyl violet, and 20-150 μmol L(-1) and 8.1 μmol L(-1) for orange II. A persulfate treatment of a spiked wastewater sample was satisfactorily monitored with the new method. 相似文献
690.