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881.
882.
Andrew Dravnieks Frank Jarke 《Journal of the Air & Waste Management Association (1995)》2013,63(12):1284-1289
Abstract Combustion flue gases of three different industrial boilers firing miscellaneous fuels were monitored for a twoweek period. Nitric oxide (NO), sulfur dioxide (SO2), carbon monoxide (CO), carbon dioxide (CO2), and total hydrocarbons (CxHy) were continuously measured using single-component gas analyzers in parallel with a lowresolution Fourier Transform Infrared (FTIR) gas analyzer. Hydrogen chloride (HCl) was measured continuously using the FTIR analyzer and semi-continuously using a traditional liquid-absorption technique. Nitrous oxide (N2O), nitrogen dioxide (NO2), and water vapor (H2O) were continuously measured using the FTIR analyzer only. Laboratory tests were conducted prior to the field measurements to assess the detection limits of the different measurement methods for each gas component. No significant differences were found between the results of the low-resolution FTIR analyzer and the single-component analyzers or the liquid absorption method. 相似文献
883.
Frank E. Butler Joseph E. Knoll M. Rodney Midgett 《Journal of the Air & Waste Management Association (1995)》2013,63(5):581-584
Techniques were developed to sample and analyze the Cr content of participate samples with emphasis on determining the concentration of the carcinogen Cr+6. Cr+6 is extracted to alkaline solution and analyzed colorimetrically. Residual particles are extracted with acid solution to remove soluble Cr+3, which is determined by atomic absorption spectrometry. This methodology was tested on samples from three diverse types of sources: a ferrochrome smelter, a chemical plant, and a refractory brick plant. Identical quadruplicate samples were collected to determine accuracy and precision of the collection and analysis procedures, and extraction of Cr+6 and Cr+3. A statistical analysis revealed that the precision of Cr+6 analysis is comparable to that of the particulate mass determination. The stability of Cr+6 In particulate form and in solution was determined. Size resolved particulate samples were collected to determine the particle size versus the Cr+6 content. At the ferrochrome smelter and the chemical plant the majority of the Cr+6 was contained in the respirable particles. The accuracy and completeness of the chemical methods employed were verified by neutron activation analysis, x-ray photoelectron spectroscopy, and scanning electron microscopyenergy dispersive x-ray analysis. 相似文献
884.
885.
Frank J. Schenck Vinetta Howard‐King 《Journal of environmental science and health. Part. B》2013,48(1):1-12
Abstract A multiresidue solid‐phase extraction (SPE) method for the isolation and subsequent gas Chromatographie determination of organochlorine and organophosphorus pesticide residues in low‐moisture, nonfatty products is described. Residues are extracted from samples with an acetonitrile/water mixture. Cleanup of the extract is performed using graphitized carbon black and anion exchange SPE columns, and analysis is performed by gas chromatography with Hall electrolytic conductivity and flame photometric detection. Recovery data was obtained by fortifying corn, oats and wheat with pesticides. The average recoveries were 79–123% for eight organochlorine and 51–122% for 28 organophosphorus pesticide residues. The limit of quantitation for chlorpyriphos was 0.05 ppm using the Hall electrolytic conductivity detector and <0.005 ppm using the flame photometric detector. 相似文献
886.
Edgar R. Stephens Frank R. Burleson 《Journal of the Air & Waste Management Association (1995)》2013,63(12):929-936
The diversity of hydrocarbons which are present in ambient polluted air provide a potentially rich source of information concerning the nature of this type of pollution. Measurements of the relative amounts of various hydrocarbons can be correlated with the various possible sources. Since hydrocarbon reactivities vary widely it is also possible to estimate the extent to which various individual hydrocarbons have reacted. Except for samples taken deliberately near sources of hydrocarbon pollution these air samples invariably resemble auto exhaust with an addition of natural gas and of C3–C5 paraffins which resemble gasoline vapor. Samples taken in industrial areas and near the smoke plume from a brush fire showed distinctive differences in composition. During the smog season in the fall of 1968 good data were obtained of “typical” or “representative” samples of light, medium and heavy smog. These show the expected depletion of more reactive hydrocarbons in a much more convincing way than before. By comparing these distributions with composition in unreacted samples and by making use of data from bottle irradiations, it was possible to estimate the contribution of the various hydrocarbons in terms of “amount reacted.” The amounts of higher hydrocarbons present and reacted were also estimated from gasoline composition. 相似文献
887.
Frank L. Heaney 《Journal of the Air & Waste Management Association (1995)》2013,63(8):617-620
A new incineration plant has replaced the sanitary landfill in Braintree, Mass. Designed in 1966 and completed in 1971 it includes sophisticated air pollution controls although existing laws or codes did not require them. The results of dust loading tests conducted by an independent organization are presented. 相似文献
888.
Frank E. Augustine Richard W. Boubel 《Journal of the Air & Waste Management Association (1995)》2013,63(6):617-621
Size distributions of particles at several downwind points in a Kraft paper mill plume have been determined by means of airborne sampling. Size distributions from samples close to the stack were found to have a log normal frequency distribution, but significant deviations from the log normal were found farther downwind. Several possible physical mechanisms are postulated as causes for this behavior. Plume dilution with background particles appears to be the most likely mechanism. The airborne sampling system is described, and electron micrographs of sampled particles are presented. 相似文献
889.
Frank F. Scherr Ajit K. Sarmah 《Journal of environmental science and health. Part. B》2013,48(8):763-772
A simple and robust analytical method was developed to simultaneously detect and quantify 17β-estradiol (E2), estrone (E1), 17β-estradiol-3-sulphate (E2-3S), and estrone-3-sulphate (E1-3S) in aqueous solutions (calcium chloride and artificial urine solutions) and agricultural soils using high performance liquid chromatography and UV detection. The standards for all four compounds were linear in the range of 0.01 to 1.0 μg mL?1 (n = 6) and 1.0 to 20 μg mL?1 (n = 6), respectively, with correlation coefficients > 0.999. The on-column limits of detection at an injection volume of 50 μL and S/N (signal: noise) ratio of 3 were: 9.0 ng mL?1, 10 ng mL?1, 5.0 ng mL?1, and 7.0 ng mL?1 for E2-3S, E1-3S, E2 and E1, respectively. The limit of detection and quantification in artificial urine solution and CaCl2 solution was 1.0 ng mL?1 for all four compounds. Method detection limits for the compounds in the 3 soils ranged from 2 to 2.4 ng g?1 (E2-3S and E1-3S), and 1.0 to 2.9 ng g?1 (E2 and E1), respectively. 相似文献
890.
Soyoung Cha Frank Black Foy King 《Journal of the Air & Waste Management Association (1995)》2013,63(3):252-257
Evaluation of emerging diesel particulate emissions control technology will require analytical procedures capable of continuous or “real-time” measurement of transient organic and elemental carbon emissions. Procedures based on the flame ionlzation properties of organic carbon and the opacity or light extinction properties of elemental carbon are described, and applied for measurement of particulate emissions from diesel engines. The Instrumentation provided adequate sensitivity and time resolution for observation of the transient emissions associated with typical automobile urban driving conditions. Analytical accuracy is evaluated by comparing Integrated average results to measurements using classical gravimetric filtration and solvent extraction procedures. Mass specifc extinction coefficients are evaluated using the Beer-Lambert law. A simplified linear model relating elemental carbon concentration to opacity is also evaluated. 相似文献