全文获取类型
收费全文 | 2569篇 |
免费 | 51篇 |
国内免费 | 30篇 |
专业分类
安全科学 | 117篇 |
废物处理 | 104篇 |
环保管理 | 767篇 |
综合类 | 165篇 |
基础理论 | 559篇 |
环境理论 | 1篇 |
污染及防治 | 658篇 |
评价与监测 | 180篇 |
社会与环境 | 81篇 |
灾害及防治 | 18篇 |
出版年
2023年 | 17篇 |
2022年 | 24篇 |
2021年 | 25篇 |
2020年 | 26篇 |
2019年 | 29篇 |
2018年 | 34篇 |
2017年 | 39篇 |
2016年 | 53篇 |
2015年 | 48篇 |
2014年 | 41篇 |
2013年 | 319篇 |
2012年 | 84篇 |
2011年 | 104篇 |
2010年 | 96篇 |
2009年 | 75篇 |
2008年 | 112篇 |
2007年 | 122篇 |
2006年 | 131篇 |
2005年 | 106篇 |
2004年 | 74篇 |
2003年 | 100篇 |
2002年 | 94篇 |
2001年 | 35篇 |
2000年 | 42篇 |
1999年 | 31篇 |
1998年 | 45篇 |
1997年 | 34篇 |
1996年 | 38篇 |
1995年 | 34篇 |
1994年 | 28篇 |
1993年 | 26篇 |
1992年 | 33篇 |
1991年 | 28篇 |
1990年 | 28篇 |
1989年 | 23篇 |
1988年 | 30篇 |
1987年 | 24篇 |
1986年 | 23篇 |
1985年 | 26篇 |
1984年 | 45篇 |
1983年 | 33篇 |
1982年 | 39篇 |
1981年 | 38篇 |
1980年 | 27篇 |
1979年 | 45篇 |
1978年 | 30篇 |
1977年 | 23篇 |
1976年 | 21篇 |
1973年 | 11篇 |
1971年 | 11篇 |
排序方式: 共有2650条查询结果,搜索用时 31 毫秒
991.
Mary K. Stinson Herbert S. Skovronek William D. Ellis 《Journal of the Air & Waste Management Association (1995)》2013,63(1):96-103
A pilot-scale soil washing process, patented by BioTrol, Inc., was demonstrated on soil contaminated by wood treating waste, primarily pentachlorophenol (PCP) and creosote-derived polynuclear aromatic hydrocarbons (PAHs). Although soil washing was the main object of this demonstration, the treatment train that was evaluated included two other BioTrol technologies for treatment of waste streams from the soil washer. The three technologies were: ? The BioTrol Soil Washer (BSW)—a volume reduction process, which uses water to separate contaminated soil fractions from the bulk of the soil. ? The BioTrol Aqueous Treatment System (BATS)—a biological water treatment process. ? The Slurry Bioreactor (SBR)—a BioTrol biological slurry treatment process conducted in an EIMCO BIOLIFTtm reactor. The sandy soil at the site, consisting of less than 10 percent of fines, was well suited for treatment by soil washing. The soil washer was evaluated in two tests on soil samples containing 130 ppm and 680 ppm of PCP, respectively. The BSW successfully separated the feed soil (dry weight basis) into 83 percent of washed soil, 10 percent of woody residues, and 7 percent of fines. The washed soil retained about 10 percent of the feed soil contamination while 90 percent of the feed soil contamination was contained within the woody residues, fines, and process water. The soil washer achieved up to 89 percent removal of PCP and 88 percent of total PAHs, based on the difference between their levels in the as-is (wet) feed soil and the washed soil. PCP concentrations of 14 ppm and 87ppm in the washed soil were achieved from PCP concentrations of 130 ppm and 680ppm in the feed soil. Concentrations of total PAHs were reduced from 247 ppm to 42 ppm and 404 ppm to 48 ppm, respectively, in the two tests. The BATS degraded up to 94 percent of PCP in the process water from soil washing. PAH removal could not be determined due to low influent concentrations. The SBR achieved over 90 percent removals of PCP and 70 to 90 percent removals of PAHs from the slurry of contaminated fines from soil washing. However, steady state operation was not achieved during the single test and the results were variable. Cost of a commercial-scale soil washing, assuming use of all three technologies, was estimated to be $168 per ton of soil treated. Incineration of woody material accounts for 76 percent of the cost. 相似文献
992.
John Wooley William W. Nazaroff Alfred T. Hodgson 《Journal of the Air & Waste Management Association (1995)》2013,63(8):1114-1120
Liquid laundry and hand dish washing detergents contain volatile organic compounds, Including ethanol, that may be liberated during use and contribute to photochemical air pollution. In this study, the release of ethanol to the atmosphere during simulated household use of liquid detergents was measured. Three replicate experiments, plus a blank, were conducted In a 20-m3 environmental chamber for each of four conditions: “typical” dish washing (DT), “high-release” dish washing (DH), “typical” laundry (LT), and “high-release” laundry (LH). Average amounts of ethanol transferred to the atmosphere per use (and the fraction of ethanol used so liberated) were 32 mg (0.038) for DT, 100 mg (0.049) for DH, 18 mg (0.002) for LT, and 110 mg (0.011) for LH. Thus, a large fraction of the ethanol added to wash solutions with liquid detergents is discharged to the sewer rather than transferred to the atmosphere during use. 相似文献
993.
William F. Jaynes Stephen A. Boyd 《Journal of the Air & Waste Management Association (1995)》2013,63(12):1649-1653
Homoionic trimethylphenylammonium (TMPA)- and tetramethylammonium (TMA)-clays were prepared by Ion-exchange reactions using two smectite clays that differed in their cation exchange capacities and surface charge densities. These clays are referred to as a low-charge (SAC) and high-charge (SWa)-smectite. The organo-clays were evaluated as adsorbents of water soluble aromatic hydrocarbons including benzene, toluene, ethylbenzene, p-xylene, butylbenzene, and naphthalene. All of the aromatic hydrocarbons tested were effectively removed from water by the low-charge TMPA-smectite. The low-charge TMA-smectite was an effective adsorbent for benzene but was ineffective in the removal of the alkylbenzenes and naphthalene from water. The effect of surface charge on the adsorption properties of TMPA-smectite was pronounced. The uptake of benzene and toluene by the high-charge TMPA-smectite was greatly reduced as compared to the low-charge TMPAsmectite. These results suggest the utility of TMPA-smectite as a liner material for petroleum storage containers and waste disposal reservoirs. The use of TMPA-smectite in conjunction with Na-smectite would provide a barrier with the ability to impede the flow of water and to effectively adsorb dissolved organic contaminants. 相似文献
994.
Brady D. Lee William A. Apel Amber R. Miller 《Journal of the Air & Waste Management Association (1995)》2013,63(9):1068-1074
ABSTRACT Research was performed to demonstrate the removal of carbon tetrachloride (CT) using compost biofilters operated under methanogenic conditions. Biofilters were operated at an empty-bed residence time of 2.8 minutes using nitrogen as the atmosphere. Hydrogen and carbon dioxide were supplied as an electron donor and carbon source, respectively, during acclimation of the bed medium microbes. Once methanogenesis was demonstrated, CT flow to the biofilter was established. Biofilters were operated over a CT concentration range from 20 to 700 ppbv for 6 months. Bed medium microbes were able to remove up to 75% of the inlet CT. At excessively high CT concentrations (>500 ppmv), methane production and hydrogen utilization by the bed medium microbes appeared to be inhibited. CT removal by the biofilter decreased when the hydrogen supply was removed from the biofilter inlet, indicating that hydrogen acted as the electron donor for reductive dechlorination. The removal efficiency and relatively low empty bed residence times demonstrated by these laboratory-scale biofilters indicate that anaerobic biofiltration of CT may be a feasible full-scale process. 相似文献
995.
996.
Barbara E. Smith William J. Adamski 《Journal of the Air & Waste Management Association (1995)》2013,63(12):1204-1206
ABSTRACT Temperature-adjusted trends in 1-hr and 8-hr ozone averages were calculated for ten sites near Lake Michigan for 1980-1995. Results show that ozone trends declined similarly according to both metrics for sites on the west side of the lake. This suggests that the factors underlying the trends were similar. These factors include, among others, ozone control programs designed to address the 1-hr standard. Thus, these control programs may have been similarly effective in moving these sites toward compliance with the 8-hr standard. 相似文献
997.
Michel P. Bonin William L. Flower Ronald F. Renzi Lawrence W. Peng 《Journal of the Air & Waste Management Association (1995)》2013,63(11):902-907
Abstract Optical measurements of particle size and concentration were made at the chromium plating tank and exhaust system at a commercial hexavalent chromium plating facility. Particles were examined at three locations in the exhaust system: 1) directly at the hexavalent chromium plating bath surface, 2) at the exit of a cyclone separator located in the exhaust system approximately three to four meters downstream of the bath, and 3) in the exhaust stack, downstream of the induced draft fan and all abatement devices. Particle diameters at the bath surface ranged from 0.3 to 25 μm. Downstream of the cyclone exit and mesh pad filters, particle top sizes were approximately 5 and 0.7 mm, respectively. On a mass basis, the collection efficiency of all abatement devices was 99.997%. Assuming that droplets in the flow consist primarily of water and chromium, correcting the total particle mass flow against water content gives a chromium emission rate of 64,000 μg/hr, which compares favorably with a value of 77,000 μg/hr measured with EPA methods. This initial agreement, which should be validated through additional measurements over a broad range of flow conditions, raises the possibility of continuous monitoring for chromium metal emissions using particle size/mass as a surrogate. 相似文献
998.
Fang-Yu Yueh Ramesh C. Sharma Jagdish P. Singh Hansheng Zhang William A. Spencer 《Journal of the Air & Waste Management Association (1995)》2013,63(11):1307-1315
Abstract The analytical figure of merit of the potential of laser-induced breakdown spectroscopy (LIBS) has been evaluated for detection of trace element in liquid. LIBS data of Mg, Cr, Mn, and Re were studied. Various optical geometries, which produce the laser spark in and at the liquid sample, were tested. The calibration curves for Mg, Cr, Mn, and Re were obtained at the optimized experimental conditions with bulk liquid and in liquid jet. It was found that measurements using a liquid jet provide better detection limits than bulk liquid measurements. The limits of detection (LOD) of Mg, Cr, Mn, and Re in the present liquid jet measurement are found to be 0.1, 0.4, 0.7, and 8 ppm, respectively. The LOD of Mg using Mg 279.55 nm was compared with the values found in other liquid work. 相似文献
999.
Timothy H. Bertram Ronald C. Cohen William J. Thorn III 《Journal of the Air & Waste Management Association (1995)》2013,63(10):1473-1479
Abstract The absolute accuracy and long‐term precision of atmospheric measurements hinge on the quality of the instrumentation and calibration standards. To assess the consistency of the ozone (O3) and nitrogen oxides (NOx) standards maintained at the National Institute of Standards and Technology (NIST), these standards were compared through the gas‐phase titration of O3 with nitric oxide (NO). NO and O3 were monitored using chemiluminescence and UV absorption, respectively. Nitrogen dioxide (NO2) was monitored directly by laser‐induced fluorescence and indirectly by catalytic conversion to NO, followed by chemiluminescence. The observed equivalent loss of both NO and O3 and the formation of NO2 in these experiments was within 1% on average over the range of 40–200 nmol mol?1 of NO in excess O3, indicating that these instruments, when calibrated with the NIST O3 and NO standards and the NO2 permeation calibration system, are consistent to within 1% at tropospherically relevant mixing ratios of O3. Experiments conducted at higher initial NO mixing ratios or in excess NO are not in as good agreement. The largest discrepancies are associated with the chemiluminescence measurements. These results indicate the presence of systematic biases under these specific conditions. Prospects for improving these experiments are discussed. 相似文献
1000.
William A. McClenny Eric J. Williams Ronald C. Cohen Jochen Stutz 《Journal of the Air & Waste Management Association (1995)》2013,63(5):542-562
Abstract The capping of stationary source emissions of NOx in 22 states and the District of Columbia is federally mandated by the NOx SIP Call legislation with the intended purpose of reducing downwind O3 concentrations. Monitors for NO, NO2, and the reactive oxides of nitrogen into which these two compounds are converted will record data to evaluate air quality model (AQM) predictions. Guidelines for testing these models indicate the need for semicontinuous measurements as close to real time as possible but no less frequently than once per hour. The measurement uncertainty required for AQM testing must be less than ±20% (±10% for NO2) at mixing ratios of 1 ppbv and higher for NO, individual NOz component compounds, and NOy. This article is a review and discussion of different monitoring methods, some currently used in research and others used for routine monitoring. The performance of these methods is compared with the monitoring guidelines. Recommendations for advancing speciated and total NOy monitoring technology and a listing of demonstrated monitoring approaches are also presented. 相似文献