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以季铵盐改性硅藻土为吸油剂,采用吸附—电化学组合工艺处理拉丝废乳化液,优化了工艺条件。实验结果表明,在乳化液pH为5.0、吸油剂加入量为20 g/L、反应温度为25 ℃的最优条件下吸附除油15 min,然后在清液pH为8.5、阳极电流密度为4 A/dm2的最优条件下电化学反应4 h后,废水无色无味,COD为43 mg/L,ρ(NH3-N)=0,ρ(Cu)= 1.6 mg/L,ρ(Zn)= 3.7 mg/L,浊度为1.1 NTU,达到GB 8978—1996污水综合排放标准。 相似文献
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K.M.S. Sundaram 《Journal of environmental science and health. Part. B》2013,48(6):1215-1239
Abstract Leaching, downward mobility and persistence of tebufenozide was investigated under laboratory conditions in columns packed with forest litter and soil, after fortification with the analytical grade material (purity > 99.6%) and with two commercial formulations, RH‐5992 2F (aqueous flowable) and RH‐5992 ES (emulsion suspension). Two types of litter and soil were used: one type with relatively high amounts of sand and the other with high amounts of clay. The concentrations eluted in the leachates were lower when the analytical material (dissolved in acetone) was used for fortification, than when the two formulations (diluted with water) were used. The amount leached was higher for RH‐5992 2F than for RH‐5992 ES. The type of substrate, i.e., sandy or clay type, had only marginal influence on the amounts eluted in the leachates. Downward movement of tebufenozide from the top 2‐cm layer to the untreated middle and bottom layers (3‐cm segments) was consistently lower when the analytical material was used for fortification, than when the two formulations were used. Downward movement was higher for RH‐5992 2F than for RH‐5992 ES. Persistence of tebufenozide in substrates, maintained under submerged conditions for 70 days after leaching, indicated an initial 2‐week lag period prior to the onset of degradation. Formulation‐related differences were observed in the half‐life (DT50) values. When the analytical material was used for fortification, the DT50 ranged from ca 54 to 59 d. However, when the formulations were used for fortification, the DT50 showed a higher range, i.e., from ca 62 to 67 d for RH‐5992 2F and ca 70 to 80 d for RH‐5992 ES. Formulation ingredients appear to have caused enhanced adsorption of tebufenozide onto the substrates, thus delaying degradation. 相似文献
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介绍加拿大学者用能量概念解决化学实验室锥形瓶或烧杯,水动力学物理模拟实验室水槽以及自然界海岸线波浪破碎等不同尺度下波浪同溢油乳化行为之间关系的同化方法和针对某些特殊问题所采取的措施以及新的尝试.从物理模拟实验室尺度和自然界海岸线尺度提出一些思考问题,并从发展的角度和中国同加拿大研究设备、能力和观点上的差异,提出中国曾经开展的类似研究是否有再度崛起的可能性,使得研究成果成为溢油乳化和溢油清理科学技术的基础,并带动解决冻结水域溢油乳化现象的理论解释. 相似文献
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An attempt has been made to produce stable water–diesel emulsion with optimal formulation and process parameters and to evaluate the performance and emission characteristics of diesel engine using this stable water–diesel emulsion. A total of 54 samples were prepared with varying water/diesel ratio, surfactant amount and stirring speed and water separation was recorded after 24 and 48 hr of emulsification. The recorded data were used in artificial neural network (ANN)-particle swarm optimization (PSO) technique to find the optimal parameters to produce water–diesel emulsion for engine testing. The predicted optimal parameters were found as 20% water to diesel ratio, 0.9% surfactant and 2200 rpm of stirrer for a water separation of 14.33% in one day with a variation of 6.54% against the actual value of water separation. Water–diesel emulsion fuel exhibited similar fuel properties as base fuel. The peak cylinder gas pressure, peak pressure rise rate and peak heat release rate for water–diesel were found higher as compared to diesel at medium to full engine loads. The improved air-fuel mixing in water–diesel emulsion enhanced brake thermal efficiency (BTE) of engine. The absorption of heat by water droplets present in water–diesel emulsion led to reduced exhaust gas temperature (EGT). With water–diesel emulsion fuel, the mean carbon monoxide (CO), unburned hydrocarbon and oxides of nitrogen (NOx) emissions reduced by 8.80, 39.60, and 26.11%, respectively as compared to diesel. 相似文献
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