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The effect of pretreatment on Pd/Al2O3 catalysts for the catalytic oxidation of o-xylene at low temperature was studied by changing the pretreatment and testing conditions. The fresh and pretreated Pd/Al2O3 catalysts were characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The results showed that the pretreatment dramatically changed the Pd/PdO ratio and then significantly affected the Pd/Al2O3 activity; while the pretreatment had not much influence on Pd particle size. The Pd/Al2O3 pre-reduced at 300℃/400℃, which has fully reduced Pd species, showed the highest activity; while the fresh Pd/Al2O3, which has fully oxidized Pd species, presented the worst performance, indicating the Pd chemical state plays an important role in the catalytic activity for the o-xylene oxidation. It is concluded that metallic Pd is the active species on the Pd/Al2O3 catalyst for the catalytic oxidation of o-xylene at low temperature. 相似文献
564.
Xinyong Liu Zhi Jiang Mingxia Chen Jianwei Shi Wenfeng Shangguan Yasutake Teraoka 《环境科学学报(英文版)》2013,25(5):1023-1033
Pt supported on mesoporous silica SBA-15 was investigated as a catalyst for low temperature selective catalytic reduction(SCR) of NO by C 3 H 6 in the presence of excess oxygen.The prepared catalysts were characterized by means of XRD,BET surface area,TEM,NO-TPD,NO/C 3 H 6-TPO,NH 3-TPD,XPS and 27 Al MAS NMR.The effects of Pt loading amount,O 2 /C 3 H 6 concentration,and incorporation of Al into SBA-15 have been studied.It was found that the removal efficiency increased significantly after Pt loading,but an optimal loading amount was observed.In particular,under an atmosphere of 150 ppm NO,150 ppm C 3 H 6,and 18 vol.% O 2,0.5% Pt/SBA-15 showed remarkably high catalytic performance giving 80.1% NOx reduction and 87.04% C 3 H 6 conversion simultaneously at 140°C.The enhanced SCR activity of Pt/SBA-15 is associated with its outstanding oxidation activities of NO to NO 2 and C 3 H 6 to CO 2 in low temperature range.The research results also suggested that higher concentration of O 2 and higher concentration of C 3 H 6 favored NO removal.The incorporation of Al into SBA-15 improved catalytic performance,which could be ascribed to the enhancement of catalyst surface acidity caused by tetrahedrally coordinated AlO 4.Moreover,the catalysts could be easily reused and possessed good stability. 相似文献
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566.
Liu Zhengqian Ma Jun Zhao Lei 《Frontiers of Environmental Science & Engineering in China》2007,1(4):482-487
Catalytic ozonation of aqueous solutions of oxalic acid was examined in the presence of graphite-supported platinum catalysts.
The catalytic activity of graphite was significantly enhanced by loading platinum. The removal efficiency of oxalic acid was
3.0%, 47.6% and 99.3% for ozonation alone, graphite catalytic ozonation and Pt/graphite catalytic ozonation in 30 min under
the experimental condition, respectively. The influence of support pretreatment, solvent, impregnation time, platinum loading
amount and reduction temperature on the activity of Pt/graphite catalyst was investigated. The pretreatment of graphite support
had no effect on activity improvement of Pt/graphite catalyst. Solvent and impregnation time also no great effect on the activity.
Platinum loading amount and reduction temperature influenced the catalyst activity significantly. The optimal catalytic performance
of Pt/graphite was obtained when 1.0% platinum loading and 623 K of reduction temperature was adopted. The Pt/graphite catalyst
was used for five times with no significant decrease in its activity and more than 90% oxalic acid removal was obtained.
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Translated from Environmental Science, 2007, 28(6): 1258–1263 [译自: 环境科学] 相似文献
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569.
Zhou Zexing Yin Ling Xu JingKesearch Center for Eco-Fnvironmental Sciences Chinese Academy of Sciences.Beijing China 《环境科学学报(英文版)》1994,(1)
StudyoncatalystsforcombustionofleanCH_4ZhouZexing,YinLing,XuJingKesearchCenterforEco-FnvironmentalSciences,ChineseAcademyofSc... 相似文献
570.
采用水热法、沉淀法和溶胶凝胶法制备了3种不同形貌的CeO2催化材料,并将其用于湿式空气氧化苯酚水溶液过程中,探讨了CeO2形貌结构对催化湿式氧化苯酚水溶液性能的影响.采用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线衍射(XRD)、程序升温还原(TPR)等手段对CeO2催化材料进行了表征.结果表明,水热法制备的CeO2催化材料表现出较好催化性能,主要原因是水热法合成的CeO2呈现交错的纳米棒状结构,主要暴露(220)晶面,且沿着(220)晶向生长.在反应温度为200℃、空气压力为2MPa、苯酚初始浓度500mg/L的条件下,最终(240min)COD的去除率为95.5%. 相似文献