全文获取类型
收费全文 | 4964篇 |
免费 | 94篇 |
国内免费 | 7篇 |
专业分类
电工技术 | 176篇 |
综合类 | 2篇 |
化学工业 | 843篇 |
金属工艺 | 115篇 |
机械仪表 | 109篇 |
建筑科学 | 99篇 |
矿业工程 | 1篇 |
能源动力 | 102篇 |
轻工业 | 400篇 |
水利工程 | 26篇 |
石油天然气 | 7篇 |
无线电 | 522篇 |
一般工业技术 | 857篇 |
冶金工业 | 1349篇 |
原子能技术 | 116篇 |
自动化技术 | 341篇 |
出版年
2023年 | 17篇 |
2022年 | 34篇 |
2021年 | 72篇 |
2020年 | 43篇 |
2019年 | 47篇 |
2018年 | 57篇 |
2017年 | 41篇 |
2016年 | 68篇 |
2015年 | 42篇 |
2014年 | 85篇 |
2013年 | 225篇 |
2012年 | 126篇 |
2011年 | 204篇 |
2010年 | 137篇 |
2009年 | 168篇 |
2008年 | 173篇 |
2007年 | 149篇 |
2006年 | 168篇 |
2005年 | 139篇 |
2004年 | 135篇 |
2003年 | 149篇 |
2002年 | 131篇 |
2001年 | 99篇 |
2000年 | 91篇 |
1999年 | 139篇 |
1998年 | 493篇 |
1997年 | 341篇 |
1996年 | 254篇 |
1995年 | 136篇 |
1994年 | 131篇 |
1993年 | 144篇 |
1992年 | 62篇 |
1991年 | 58篇 |
1990年 | 60篇 |
1989年 | 54篇 |
1988年 | 49篇 |
1987年 | 32篇 |
1986年 | 53篇 |
1985年 | 59篇 |
1984年 | 39篇 |
1983年 | 41篇 |
1982年 | 39篇 |
1981年 | 44篇 |
1980年 | 40篇 |
1979年 | 27篇 |
1978年 | 17篇 |
1977年 | 28篇 |
1976年 | 48篇 |
1975年 | 13篇 |
1973年 | 13篇 |
排序方式: 共有5065条查询结果,搜索用时 31 毫秒
101.
102.
103.
Lithium naphthalene reacts with acetic acid to give α-anion of lithium acetate. The reaction of this anion with various ketones gives the corresponding β-hydroxy-acids in good yield. 相似文献
104.
Masaru Takahashi Tetsu Nakatani Shinji Iwamoto Tsunenori Watanabe Masashi Inoue 《Applied catalysis. B, Environmental》2007,70(1-4):73-79
The solvothermal reaction of mixtures of aluminum isopropoxide (AIP) and gallium acetylacetonate (Ga(acac)3) directly yielded the mixed oxides of γ-Ga2O3-Al2O3. In the solvothermal synthesis, the crystal structure of mixed oxides was controlled by the initial formation of γ-Ga2O3 nuclei. The mixed oxides prepared in diethylenetriamine have extremely high activities for selective catalytic reduction (SCR) of NO with methane as a reducing agent. With increasing crystallite size of the spinel structure, the catalytic activity increased. The ratio of the amount of methane consumed by combustion to total methane conversion was proportional to the density of acid sites on the surface of the mixed oxides. The mixed oxide catalysts prepared in diethylenetriamine had lower densities of acid sites and showed a higher methane-efficiency for CH4-SCR than those prepared in other solvents. These catalysts maintained their high activity even when the reaction was carried out under the severe conditions (i.e., high space velocity and low NO concentration). 相似文献
105.
Single-walled carbon nanotube networks grown on SiO2 pillars were studied by means of scanning photoemission microscopy. The individual nanotubes or nanotube bundles growing from the pillar tops were observed in C 1s images. Band bending near catalytic Fe/nanotube contacts in an end-bonded configuration was studied by measuring C 1s spectra along the tube axes. Within our experimental resolution, no band bending was observed. This implies that the depletion width is less than the spatial resolution of the scanning photoemission microscope (90 nm) or that the amount of the band bending is less than 0.1 eV. 相似文献
106.
The crystalline complex between poly(γ-methyl l-glutamate) (PMLG) and dimethyl phthalate (DMP) has been formed in films cast from a solution in dichloroethane. It has the stoichiometry of 1 mol of DMP to three or four residues of PMLG and shows two definite characteristics in X-ray diffraction patterns; one is the large hexagonal unit cell with the edge of around 28 Å and another the ‘extra’ 5.07 Å meridional reflection which can not be interpreted by a PMLG α-helical conformation. The structural examination for the films with various DMP contents is carried out by X-ray, viscoelastic, and d.s.c. measurements and the following structure is proposed for the crystalline complex. Four PMLG are associated to form a group which is hexagonally packed and DMP molecules, located in the gaps between groups, form a specific favourable helical structure along PMLG chains in which the van der Waals stacking of benzene rings of DMP is significant. 相似文献
107.
N. Mizuochi M. Ogura H. Watanabe J. Isoya H. Okushi S. Yamasaki 《Diamond and Related Materials》2004,13(11-12):2096
Boron-doped p-type single crystalline chemical vapor deposition (CVD) homoepitaxial diamond films were investigated by electron paramagnetic resonance (EPR). Carbon dangling bond defects, which were accompanied by a nearby hydrogen atom, were observed in boron-doped p-type CVD diamond films on a IIa substrate similar to those observed in undoped diamond. This result suggested that the energy level position of the defects is located below the Fermi energy of boron-doped diamond, at around 0.3 eV above the valence-band top. The reason why the Fermi energy could be changed by the incorporation of boron atoms at low density (1016–1017/cm3) in the film in spite of the existence of the large defect density of EPR centers (1018/cm3) is thought to be that the singly occupied electron states of defects are located near the band edge. As for the thermal annealing effect of the defects, it was revealed that the concentration of the defects and the mobility of the p-type film did not change after annealing up to 1200 °C which is much higher than the temperature of boron–hydrogen pair dissociation. 相似文献
108.
Praphan?Pinsirodom Yomi?Watanabe Toshihiro?Nagao Akio?Sugihara Takashi?Kobayashi Yuji?ShimadaEmail author 《Journal of the American Oil Chemists' Society》2004,81(6):543-547
Production of MAG by a lipase-catalyzed reaction is known to be effective at low temperature. This phenomenon can be explained
by assuming that synthesized MAG are excluded from the reaction system because MAG, which have low m.p., are solidified at
low temperatures. Consequently, MAG are efficiently accumulated and do not serve as the precursor of DAG. If this hypothesis
is correct, the critical temperature for MAG production, defined as the highest temperature at which DAG synthesis is repressed,
should depend on the m.p. of the MAG. Esterification of FFA with glycerol using Candida rugosa, Rhizopus oryzae, and Penicillium camembertii lipases produced MAG efficiently at low temperatures. However, Candida lipase showed very low esterification activity at high temperatures (>20°C), and Rhizopus lipase produced not only MAG but also DAG even at low temperatures. Meanwhile, P. camembertii lipase catalyzed synthesis of MAG only from FFA and glycerol at low temperatures, although the enzyme catalyzed synthesis
of DAG from MAG in addition to synthesis of MAG at high temperatures. We thus studied the effect of temperature on esterification
of C10−C18 FFA with glycerol using Penicillium lipase as a catalyst and determined the critical temperatures for production of MAG. The critical temperature for production
of each MAG showed a linear correlation with m.p. of the MAG, which supported the hypothesis. In addition, because the m.p.
of MAG are estimated from that of the constituent FA, the optimal temperature for production of MAG can be predicted from
the m.p. of the FFA used as a substrate. 相似文献
109.
The compositions of ester- and amide-linked fatty acids from ceramides of human vernix caseosa were described with emphasis
on the distribution of the branched-chain fatty acid (BCFA). Two novel ceramides were isolated from vernix caseosa in the
course of this study: the acylated type of esterified α-OH-hydroxyacid/sphingosine ceramide (Cer[EAS]) and nonacylated type
of non-OH fatty acid/hydroxysphingosine ceramide (Cer[NH]). Their chemical structures were identified by nuclear magnetic
resonance and chemical procedure. The Cer[EAS] was an acylceramide and consisted of the highest concentrations of ester- and
amide-linked BCFA (62 and 67%, respectively). The iso- or anteiso-branching structures of the aliphatic chains were confirmed
by the mass spectra of their picolinyl or pyrrolidide derivatives. As a whole, amide-linked fatty acids of ceramides 1–7 and
Cer[NH] were normal types of straight-chain fatty acids with or without α- or ω-hydroxylation. The BCFA concentrations of
amide-linked fatty acids in these ceramides (ceramides 1–7 and Cer[NH]) were low and less than 10%. The BCFA thus occurred
exclusively in a novel acylceramide of Cer[EAS] in the vernix caseosa. 相似文献
110.
S. Mitsui M. Shionoya K. Gohke F. Watanabe S. Imaizumi Y. Senda 《Journal of Catalysis》1975,40(3):372-378
In order to investigate the steric effect of the substituents to determine the product distribution, disubstituted cyclohexenes were hydrogenated over several transition metal catalysts. Some cyclohexenes which have two large substituents at the vicinal carbon atoms, at least one of which is trigonal, were not hydrogenated over Raney Ni at all but were hydrogenated over Pt catalyst under our experimental conditions. Presumably, the stereoselectivity depends on the competitive operation of the torsional angle strain and the catalyst hindrance with substituents. In the hydrogenation over Pd catalyst, thermodynamically more stable products were dominant at the standard condition but at high substrate to catalyst ratio the less stable products were slightly preferred. No appreciable stereoselectivity was observed in the hydrogenation of 1,4-disubstituted cyclohexenes. 相似文献