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101.
用于甲烷分解和甲烷二氧化炭重整的碳材料催化剂研究进展 总被引:1,自引:0,他引:1
The decomposition and CO2 reforming of methane,respectively,are promising alternatives to industrial steam methane reforming. In recent years,research has been focused on the development of catalysts that can operate without getting deactivated by carbon deposition,where,in particular,carbon catalysts have shown positive results. In this work,the role of carbon materials in heterogeneous catalysis is assessed and publications on methane decomposition and CO2 reforming of methane over carbon materials are reviewed. The influence of textural properties(BET surface area and micropore volume,etc.) and oxygen surface groups on the catalytic activity of carbon materials are discussed. In addition,this review examines how activated carbon and carbon black catalysts,which are the most commonly used carbon catalysts,are deactivated. Characteristics of the carbon deposits from methane are discussed and the influence of the reactivity to CO2 of fresh carbon and carbonaceous deposits for high and steady conversion during CO2 reforming of CH4 are also considered. 相似文献
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采用浸渍法制备了介孔Al2O3(M-Al2O3)负载PdO催化剂,考察了其催化CH4燃烧反应性能.结果表明,以M-Al2O3为载体的PdO催化剂活性比普通Al2O3载体高得多,这很可能与M-Al2O3的孔道结构对PdO物种的限域作用有关.随着PdO/M-Al2O3催化剂焙烧温度的升高,甲烷催化燃烧活性先增加后降低,其中700oC焙烧的催化剂活性最高,400oC反应时CH4转化率为91%.此时Pd物种主要以PdO颗粒形式高度分散在载体的介孔孔道内,而高温焙烧时,Pd物种主要以Pd和PdO的混合晶相存在.尽管900oC焙烧制得的催化剂上CH4的转化率降低,但TOF值最大,这可能与该催化剂中同时存在金属Pd和PdO有关. 相似文献
107.
煤层气(矿井瓦斯)是一种有望替代传统化石燃料,如煤、石油和天然气的非常规气体. 作为可得的清洁能源,它的利用被认为是节能和经济的选择. 在本工作中,非金属原子X(X=H,O,N,S,P,Si,F,Cl)修饰的石墨烯(Gr)被用来代表具有结构异性的煤表面模型. 通过密度泛函理论系统地研究了煤层气组分Y(Y=CH4,CO2,H2O)在非金属原子修饰石墨烯上的吸附作用. 结果表明Y在非金属原子修饰石墨烯上的吸附均为物理吸附. 态密度和差分电荷密度共同表明了这种弱的相互作用.其中,H和Cl对CH4的作用较大; N、O、F、Cl对CO2的作用较强; N,Cl对H2O的影响不容忽视. 总的来说,吸附能大小依次为:H2O>CO2>CH4. 因此,在CH4富集的煤层里注入H2O或CO2可以与CH4形成竞争吸附,进而提高煤层气采收率. 本工作提供了在分子水平下煤层气与非金属原子修饰石墨烯之间的相互作用的详情,并为煤层瓦斯的开采与分离提供了有用的信息. 相似文献
108.
Florian Blasberg 《Journal of organometallic chemistry》2011,696(23):3593-3600
The synthesis, structural characterization, and coordination behavior of ditopic ortho-hydroquinone-based bis(pyrazol-1-yl)methane ligands (ortho-(OH)2C6H3-4-CHpz2, ortho-(OH)2C6H3-4-CH(3-Phpz)2, and ortho-(OH)2C6H3-4-CH(3-tBupz)2) with pyrazole, 3-phenylpyrazole, and 3-tert-butylpyrazole as donors are described. The reaction of a soluble PdCl2-source with ortho-(OH)2C6H3-4-CHpz2 in acetonitrile yielded the related square-planar N,N-coordinated Pd(II) dichloride complex, whereas treatment of ortho-(OH)2C6H3-4-CH(3-Phpz)2 or ortho-(OH)2C6H3-4-CH(3-tBupz)2 with PdCl2 in acetonitrile resulted in degradation of these ligands. The Pd(II) complexes trans-(3-PhpzH)2PdCl2 and trans-(3-tBupzH)2PdCl2 were isolated and fully characterized including X-ray diffraction analyses. 相似文献
109.
Ke Ding 《Journal of organometallic chemistry》2011,696(23):3662-3667
Reactions of 2-hydroxyphenyl and 2-methoxyphenylbis(pyrazol-1-yl)methanes as well as 2-hydroxyphenyl and 2-methoxyphenylbis(3,5-dimethylpyrazol-1-yl)methanes with W(CO)5THF have been carried out. Heating 2-hydroxyphenylbis(pyrazol-1-yl)methane (L1) with W(CO)5THF in THF at reflux yielded complex (L1)W(CO)4.L1, while similar reaction of 2-hydroxyphenylbis(3,5-dimethylpyrazol-1-yl)methane (L2) with W(CO)5THF resulted in the cleavage of a Csp3-N bond to generate 1,2-bis(2-hydroxyphenyl)-1,2-bis(3,5-dimethylpyrazol-1-yl)ethane (L) and pyrazole derivative W(CO)5(3,5-Me2PzH) (Pz = pyrazol-1-yl). These two fragments were connected together through strong O…H-N and O-H…N hydrogen bonds to form complex L.[W(CO)5(3,5-Me2PzH)]2. The analogous results were observed in the treatment of 2-methoxyphenylbis(pyrazol-1-yl)methane (L3) with W(CO)5THF, which gave product L′.[W(CO)5(PzH)]2 (L′ = 1,2-bis(2-methoxyphenyl)-1,2-bis(pyrazol-1-yl)ethane) as well as certain amount of complex (L3)W(CO)4. In addition, during the reaction of 2-methoxyphenylbis(3,5-dimethylpyrazol-1-yl)methane (L4) with W(CO)5THF, partial decomposition reactions took place to yield complexes (L4)W(CO)4 and W(CO)5(3,5-Me2PzH), but no hydrogen bond was found between these two moieties. 相似文献
110.
A comprehensive kinetic model for oxidative coupling of methane(OCM)over Mn and/or W promoted Na2SO4/SiO2 catalysts was developed based on a micro-catalytic reactor data.The methane conversion and ethylene,ethane,carbon monoxide and carbon dioxide selectivities were obtained in a wide operating condition range of 750 - 825-C,CH4/O2=2.5 - 10 and contact time=267 - 472 kg s m-3.Reaction networks of six models with different rate equation types were compared together.The kinetic rate parameters of each reaction network were estimated using linear regression or genetic algorithm optimization method(GA).A reaction network suggested by Stansch et al.for OCM was found to be the best one and was further used in this work.The suggested model could predict the experimental results of OCM reaction within a deviation range of ± 20%. 相似文献