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61.
Joongjai Panpranot Sujaree Kaewgun and Piyasan Praserthdam 《Reaction Kinetics and Catalysis Letters》2005,85(2):299-304
Summary The pore structure of silica supports (SiO2 or MCM-41) has little influence on the metal-support interaction in silica supported cobalt catalysts. Cobalt dispersion, reduction behavior, and catalytic properties for the Fischer-Tropsch synthesis were primarily affected by the metal particle size. 相似文献
62.
Jia Hui Xu Ting Ting Zhuang Yi Cao Dr. Jing Yang Jing Jia Wen Zheng Ying Wu Dr. Chun Fang Zhou Dr. Li Huang Ying Wang Prof. Dr. Ming Bo Yue Dr. Jian Hua Zhu Prof. Dr. 《化学:亚洲杂志》2007,2(8):996-1006
Copper oxide was incorporated into MCM‐41 by a one‐pot synthesis under acidic conditions to prepare a new mesoporous nitrosamines trap for protection of the environment. The resulting composites were characterized by XRD, N2 adsorption–desorption, and H2 temperature‐programmed reduction techniques, and their adsorption capabilities were assessed in the gaseous adsorption of N‐nitrosopyrrolidine (NPYR). The adsorption isotherms were consistent with the Freundlich equation. The copper salt was deposited onto MCM‐41 during the evaporation stage and was fixed on the host in the calcination process that followed. MCM‐41 was able to capture NPYR in air below 373 K but not at 453 K. Loading of copper oxide on MCM‐41 greatly improved its adsorption capability at elevated temperatures. The influence of the incorporation of copper into MCM‐41 samples and the adsorption behavior of these samples are discussed in detail. 相似文献
63.
64.
负载型纳米TiO2复合载体及其CoMo催化剂的酸性及孔特性的研究 总被引:3,自引:0,他引:3
总结了复载不同纳米尺度的复合载体及其CoMo催化剂的表面酸性及孔结构特性的表征结果。结果表明,负载型纳米TiO2与基载体γ-Al2O3存在着相互作用。当负载比较少量的纳米TiO2时,复合载体的总酸量随着TiO2含量的增加而增加,超过γ-Al2O3的酸量,但当 TiO2的含量比较高时复合载体的酸量又降低,纳米TiO2优先负载在γ-Al2O3的强酸中心位;负载了CoMo活性组分后酸量增加。不同粒径的纳米TiO2对复合载体和催化剂的酸分布没有明显影响,但对总酸量有影响。对不同尺度TiO2,随着TiO2负载量的增加以及负载金属活性组分的增加,表面积、孔容和最可几孔径均有不同程度的减少。 相似文献
65.
Yoshizumi Ishikawa Hideyasu Honda Yoshiyuki Sugahara 《Journal of Sol-Gel Science and Technology》2000,19(1-3):365-369
The conversion of tetrakis(diethylamino)titanium (Ti(NEt2)4) into titania via either a combination of hydrolysis (Ti(NEt2)4 : THF : H2O = 1 : 10 : x, x = 2, 4, 10) at ambient conditions and calcination (method A) or hydrolysis in a water-tetrahydrofuran (THF) mixture (Ti(NEt2)4 : THF : H2O = 1 : 10 : 100) at reflux (method B) was investigated. Titanium tertiary butoxide (Ti(O
t
Bu)4) was also used as a substitute for Ti(NEt2)4. The hydrolysis via method A resulted in the formation of amorphous solids containing organics. Thermal analyses showed that the hydrolysis products showed mass losses up to 500°C probably due to the presence of diethylamine (Et2NH) formed via the hydrolysis of Ti(NEt2)4 in the hydrolysis products, while a mass loss of the hydrolysis product from Ti(O
t
Bu)4 was completed up to about 200°C. After calcination at 600°C, anatase or a mixture of anatase and rutile was obtained. The crystallization behavior of the hydrolysis products from Ti(NEt2)4 was different from that of the hydrolysis product from Ti(O
t
Bu)4. The hydrolysis via method B gave only an amorphous material from Ti(NEt2)4, while a crystalline titania (anatase and brookite) formed from Ti(O
t
Bu)4. 相似文献
66.
Sol-gel-derived titania films were analyzed by temperature programmed desorption (TPD) and X-ray diffraction (XRD) techniques.
The relationship between the TPD curves measured for two types of titania gel films and their crystal structures was investigated.
On the basis of the analyses, a preparation process for a titania sol solution containing anatase nanocrystals was designed
and developed. Using this process, a colloidal anatase titania sol solution was prepared by heating aqueous titanium hydroxide
containing HCl at 60°C for 2 h. The nanocrystal structure of the titania films obtained by coating the sol on glass substrates
was confirmed by TPD and XRD measurements. 相似文献
67.
TiO2/Eu-MCM纳米超分子材料的组装和光催化性能 总被引:1,自引:0,他引:1
利用有机相-水相界面共沉淀溶胶支持自组装方法制备粒径为15 nm、孔径为8 nm的分子筛Eu-MCM, 它拥有734 m2/g的比表面积和1.49 cm3/g的比孔容. 把TiO2组装到Eu-MCM的孔道中, 组装成TiO2/Eu-MCM纳米复合材料. XRD, RAMAN和选区电子衍射花样分析表明纳米复合材料中的TiO2为锐钛型. TiO2/Eu-MCM的发光表现为Eu3+离子的特征光谱, 激发峰分别为342 (5L10), 358 (5L9), 378 (5L7), 390 (5L6), 411 (5D3), 462 (5D2)和524 (5D1) nm; 发射峰为579, 592, 613, 653和701 nm, 归属于5D0→7FJ (J=0, 1, 2, 3, 4)组态间的跃迁. 纳米复合材料的发光强度都要比Eu-MCM的发光强, 其中43%TiO2/Eu-MCM的发光最强. 荧光和紫外漫反射结果表明客体TiO2对主体分子筛存在能量传递效应. 在微弱的紫外灯光照射下, TiO2/Eu-MCM纳米复合材料对苯酚的光催化氧化性能和其发光强度具有一定的相关性. 29%TiO2/Eu-MCM的纳米复合材料拥有的比表面积、孔容和孔径分别为204 m2/g, 0.24 cm3/g和4.7 nm. 29%TiO2/Eu- MCM对苯酚具有68%的最高光催化氧化产率和85%催化氧化选择性. 相似文献
68.
69.
锐钛相虫蛀状介孔二氧化钛的表征 总被引:3,自引:0,他引:3
0IntroductionMesostructuredtitania(TiO2)hasattractedagreatdealofattention,inviewofcontrolleddelivery,catalytic,photocatlytic,orenergyconversionapplica-tions犤1犦.Theuseoftitaniumisopropoxidebis-acetylace-tonateprecursors,combinedwithalkylphosphatean-ionicsurfactantsastemplate,ledtothefirstdocu-mentedpuremesoporousTiO2犤2犦.Insubsequentyears,moresyntheticstrategieshavebeendevelopedusingavarietyofstructure-directingagents,forexample,car-boxylicacids犤3犦,alkylamine犤4犦,aminium犤5犦,blockcop-o… 相似文献
70.
Vera P. Shmachkova Nina S. Kotsarenko Vladislav V. Kanazhevskiy Galina N. Kryukova Dimitri I. Kochubey Jacques Vedrine 《Reaction Kinetics and Catalysis Letters》2007,91(1):177-185
Methods of the preparation of catalysts for alkane skeletal isomerization based on uniform nanoparticles of sulfated zirconia
anchored to different supports were investigated. These catalysts were characterized by using the ICP, HRTEM and BET techniques.
The activities of the catalysts in the reaction of n-butane isomerization were measured and compared with those of bulk catalysts. 相似文献