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91.
Tank fires threaten the lives of people and pollute the environment for their intense radiant heat, rapid fire spread and explosion hazard. Compressed air/nitrogen foam (CAF/CNF), a cleaner fire extinguishing technique used for the tank fire suppression because halogen-based agents were prohibited for environmental reasons. In this work, the influence of foaming gas in CAF/CNF on extinguishing the n-heptane tank fire was firstly investigated. Firstly, it was found that CNF spreads faster with rapid increase in foam thickness, mainly due to its better stability and less evaporation. Secondly, after foam was discharged, there existed a short increase of the combustion intensity, associated with three monotonous regions and two time delays in the whole extinguishing time. The two time delays were caused by Rayleigh–Taylor instability and flame sheet shift, respectively, and the shift distance was larger for CNF. Finally, the influential factors contributing to flame extinction were exhibited to be mainly related to the decrease in liquid burning rate and gas-phase Damkohler number. Among these factors, foam spreading rate and thickness dominated due to coupled chemical and physical extinguishing effects. Resulted from some competitive effects, CNF was slightly more efficient at extinguishing tank fires than CAF. 相似文献
92.
防灭火泡沫材料是1种新型的防灭火材料,对高位倾斜裂隙火灾的降温隔热、充填加固具有很好的应用性能。为了了解高位倾斜裂隙通道中泡沫流体的扩散规律,通过理论推导得出不同裂隙倾角和方位角下浆体2端面压力差随时间的变化方程式,以理论公式为基础进行修正,提出了泡沫流体的扩散规律函数式,并通过用其他实验测点进行误差对比分析。研究结果表明:误差均在允许的范围之内,证明拟合出的函数式具有普遍适用性,可以为大采空区隐蔽高温火源点的防治提供理论支持。 相似文献
93.
利用表面活性剂胶态微泡沫冲洗技术来提高四氯乙烯(PCE)在地下水的溶解性和流动性,提高污染物迁移通量,强化去除效果.主要工艺参数和影响因素对泡沫稳定性的影响,结果表明4000r/min的搅拌转数即可产生稳定的胶态微泡沫,泡沫稳定性随表面活性剂浓度增大有小幅度提高,PCE对泡沫稳定性有不利影响;胶态微泡沫在含水层的迁移规律表明,泡沫前端迁移时不断破裂并气液分离,形成气体在上部,液体在下部,后续泡沫稳定向前推流的迁移模式,泡沫在含水层中受到地下水的静水压力,与在土壤迁移相比其体系压力更大,泡沫破裂更严重、迁移速率更慢;和液体冲洗相比,泡沫冲洗对PCE增溶增流效果明显,介质粒径为0.1~0.25mm、0.25~0.5mm和0.5~1mm时,PCE去除率分别达到83.7%、90.8%和98.2%,介质粒径越大,去除效果越明显. 相似文献
94.
在氩气气氛下,经高温煅烧三聚氰胺海绵(MS),制备了碳化三聚氰胺海绵(HMS),利用SEM、XPS、FI-IR对HMS的碳化情况进行分析,测定了海绵碳化前后的密度、亲水性、孔隙率、吸收光谱及压缩回弹性能.结果表明,MS部分碳化形成HMS,疏水性增强且亲油性不变,孔隙率略有降低,具有优异的吸光性能及机械性能.HMS海绵对轻质油品和重油吸附实验的结果显示:HMS海绵对轻质油品饱和吸附体积为92.20cm3/g;在一个太阳光(1kW/m2)照射下,HMS海绵温度快速升高,有效降低底面接触的重油粘度并加快吸附重油速度,吸附量高达99.1g/g左右;利用HMS海绵重复对重油进行10次吸附-挤压脱附,发现其对重油的饱和吸附量可保持在81.00 g/g以上.这些特性使得HMS海绵成为一种有前景的高效节能、可重复利用的石油泄漏吸附剂. 相似文献
95.
R. Grover A.J. Cessna L.A. Kerr 《Journal of environmental science and health. Part. B》2013,48(1):113-128
Abstract Analytical procedures for the simultaneous determination of residues of 2,4‐D and dicamba from polyurethane foam plug air samplers, ethylene glycol impregnated glass‐fiber filter paper dermal samplers, 1% sodium bicarbonate hand wash solution, and urine are presented. Residues were derivatized with diazomethane and quantitated using electron capture gas chromatography. Recoveries were greater than 80% at the limit of detection in all substrates. The limits of detection for both herbicides were 0.1 μg/foam plug and 0.5 μg/filter paper, and in the urine, 1.7 μg/100 mL and 5.0 μg/100 mL for dicamba and 2,4‐D, respectively. 相似文献
96.
Both long duration (>6 h) and high temperature (up to 139 °C) sampling efforts were conducted using ambient air sampling methods to determine if either high volume throughput or higher than ambient air sampling temperatures resulted in loss of target polychlorinated dibenzodioxins/dibenzofurans (PCDDs/PCDFs) from a polyurethane foam (PUF) sorbent. Emissions from open burning of simulated military forward operating base waste were sampled using EPA Method TO-9A for 185 min duration using a filter/PUF/PUF in series combination. After a 54 m3 sample was collected, the sampler was removed from the combustion source and the second PUF was replaced with a fresh, clean PUF. An additional 6 h of ambient air sampling (171 m3) was conducted and the second PUF was analyzed to determine if the PCDD/PCDF transferred from the filter and the first PUF. Less than 4.4% of the initial PCDD/PCDF was lost to the second PUF. To assess the potential for blow off of PCDD/PCDF analytes during open air sampling, the mobility of spiked mono- to hepta-PCDD/PCDF standards across a PUF sorbent was evaluated from ambient air temperatures to 145 °C with total volumes between 600 L and 2400 L. Lower molecular weight compounds and higher flow amounts increased release of the spiked standards consistent with vapor pressure values. At 600 L total sampled volume, the release temperature for 1% of the tetra-CDD (the lowest chlorinated homologue with a toxic compound) was 87 °C; increasing the volume fourfold reduced this temperature to 73 °C. 相似文献
97.
研究了氟碳表面活性剂添加量、氟碳表面活性剂性质和泡沫液浓度等对空心微珠三相泡沫在油面稳定性的影响,并在模拟燃烧装置上对比了添加氟碳表面活性剂前后三相泡沫的抗烧能力.结果表明,加入氟碳表面活性剂后,三相泡沫在油面的稳定性显著增强,且阴离子氟碳表面活性剂优于阳离子和两性离子表面活性剂.当阴离子氟碳表面活性剂、空心玻璃微珠和蛋白泡沫浓度分别为0.02%、6%和10%时,三相泡沫受热后表面形成黑色致密覆盖层,可有效隔绝热量向内部传递,使抗烧性得到明显提高. 相似文献
98.
99.
Ana Isabel Barrado Susana García Marisa Luisa Sevillano Jose Antonio Rodríguez Enrique Barrado 《Chemosphere》2013
Thirteen PAHs, five nitro-PAHs and two hydroxy-PAHs were determined in 55 vapor-phase samples collected in a suburban area of a large city (Madrid, Spain), from January 2008 to February 2009. The data obtained revealed correlations between the concentrations of these compounds and a series of meteorological factors (e.g., temperature, atmospheric pressure) and physical–chemical factors (e.g., nitrogen and sulfur oxides). As a consequence, seasonal trends were observed in the atmospheric pollutants. A “mean sample” for the 14-month period would contain a total PAH concentration of 13 835 ± 1625 pg m−3 and 122 ± 17 pg m−3 of nitro-PAHs. When the data were stratified by season, it emerged that a representative sample of the coldest months would contain 18 900 ± 2140 pg m−3 of PAHs and 150 ± 97 pg m−3 of nitro-PAHs, while in an average sample collected in the warmest months, these values drop to 9293 ± 1178 pg m−3 for the PAHs and to 97 ± 13 pg m−3 for the nitro-PAHs. Total vapor phase concentrations of PAHs were one order of magnitude higher than concentrations detected in atmospheric aerosol samples collected on the same dates. Total nitro-PAH concentrations were comparable to their aerosol concentrations whereas vapor phase OH-PAHs were below their limits of the detection, indicating these were trapped in airborne particles. 相似文献
100.