全文获取类型
收费全文 | 4444篇 |
免费 | 71篇 |
国内免费 | 8篇 |
专业分类
电工技术 | 176篇 |
综合类 | 7篇 |
化学工业 | 774篇 |
金属工艺 | 80篇 |
机械仪表 | 66篇 |
建筑科学 | 63篇 |
能源动力 | 107篇 |
轻工业 | 252篇 |
水利工程 | 20篇 |
石油天然气 | 10篇 |
无线电 | 522篇 |
一般工业技术 | 702篇 |
冶金工业 | 1328篇 |
原子能技术 | 125篇 |
自动化技术 | 291篇 |
出版年
2023年 | 19篇 |
2022年 | 62篇 |
2021年 | 72篇 |
2020年 | 30篇 |
2019年 | 40篇 |
2018年 | 36篇 |
2017年 | 33篇 |
2016年 | 65篇 |
2015年 | 27篇 |
2014年 | 78篇 |
2013年 | 153篇 |
2012年 | 107篇 |
2011年 | 153篇 |
2010年 | 106篇 |
2009年 | 129篇 |
2008年 | 132篇 |
2007年 | 114篇 |
2006年 | 111篇 |
2005年 | 98篇 |
2004年 | 105篇 |
2003年 | 102篇 |
2002年 | 90篇 |
2001年 | 122篇 |
2000年 | 91篇 |
1999年 | 130篇 |
1998年 | 549篇 |
1997年 | 335篇 |
1996年 | 241篇 |
1995年 | 128篇 |
1994年 | 135篇 |
1993年 | 112篇 |
1992年 | 63篇 |
1991年 | 55篇 |
1990年 | 54篇 |
1989年 | 52篇 |
1988年 | 53篇 |
1987年 | 49篇 |
1986年 | 46篇 |
1985年 | 45篇 |
1984年 | 37篇 |
1983年 | 37篇 |
1982年 | 40篇 |
1981年 | 44篇 |
1980年 | 23篇 |
1979年 | 30篇 |
1978年 | 20篇 |
1977年 | 30篇 |
1976年 | 53篇 |
1973年 | 17篇 |
1972年 | 13篇 |
排序方式: 共有4523条查询结果,搜索用时 15 毫秒
71.
Thermophysical properties of molten semiconductors are reviewed. Published data for viscosity, thermal conductivity, surface tension, and other properties are presented. Several measurement methods often used for molten semiconductors are described. Recommended values of thermophysical properties are tabulated for Si, Ge, GaAs, InP, InSb, GaSb, and other compounds. This review shows that further measurements of thermophysical properties of GaAs and InP in the molten state are required. It is also indicated that a very limited amount of data on emissivity is available. Space experiments relating to thermophysical property measurements are described briefly.Nomenclature
Density
-
C
p
Specific heat
-
Kinematic viscosity
-
Dynamic viscosity=
-
Thermal diffusivity
-
Thermal conductivity=Cp
-
Volumetric thermal expansion coefficient
-
Surface tension
-
d/dT
Temperature coefficient of surface tension
-
g
Gravitational acceleration
-
T
Temperature
-
T
Temperature difference
-
L
Characteristic dimension 相似文献
72.
Yoshiro Nakamura Akira Watanabe Kunio Mori Kosaku Tamura Michio Inagaki 《Journal of Materials Science》1986,21(12):4485-4488
A binary blend which consists of two incompatible polymers such as poly(vinyl chloride) and polyethylene has been performed through a partial co-crosslinking reaction with peroxide to give a co-crosslinked blend with a uniform dispersion of small polyethylene particles and with an improved mechanical property. The results are obtained through the formation of a co-crosslinked product which acts as a potential solid phase dispersant as well as a well-bonded reinforcing interlayer on polyethylene particles uniformly dispersed in poly(vinyl chloride) matrix. The resulting blends (PVC/PE=10/90 wt) give carbon spherules of 0.5 to 1m diameter through pressure-carbonization at 650° C for 1 h. 相似文献
73.
Dr. Daisuke Fujiwara Kousuke Mihara Ryo Takayama Yusuke Nakamura Prof. Mitsuhiro Ueda Prof. Takeshi Tsumuraya Prof. Ikuo Fujii 《Chembiochem : a European journal of chemical biology》2021,22(24):3406-3409
Conformationally constrained peptides hold promise as molecular tools in chemical biology and as a new modality in drug discovery. The construction and screening of a target-focused library could be a promising approach for the generation of de novo ligands or inhibitors against target proteins. Here, we have prepared a protein kinase-focused library by chemically modifying helix-loop-helix (HLH) peptides displayed on phage and subsequently tethered to adenosine. The library was screened against aurora kinase A (AurA). The selected HLH peptide Bip - 3 retained the α-helical structure and bound to AurA with a KD value of 13.7 μM. Bip - 3 and the adenosine-tethered peptide Bip - 3 - Adc provided IC50 values of 103 μM and 7.7 μM, respectively, suggesting that Bip - 3 - Adc bivalently inhibited AurA. In addition, the selectivity of Bip - 3 - Adc to several protein kinases was tested, and was highest against AurA. These results demonstrate that chemical modification can enable the construction of a kinase-focused library of phage-displayed HLH peptides. 相似文献
74.
Decomposition of t-butylhydroperoxide was retarded by triazine thiols and their zinc salts, but accelerated by the copper salts of triazine thiols as well as sulfur compounds such as dithiocarbamates and mercaptobenzothiazolates. Triazine thiols and their zine salts are effective antioxidants for polyethylene crosslinked with peroxide and containing copper, and for protecting epichlorohydrin vulcanizates against attack by “sour” or hydroperoxide-containing gasoline. 相似文献
75.
Zhongwen Wu Yubin Zheng Hongmao Yan Tomoki Nakamura Takafumi Nozawa Ryutoku Yosomiya 《大分子材料与工程》1989,173(1):163-181
Polymer blends of PEEK with PES were prepared by the solution blending method. Copolymers composed of PEEK and PES components were synthesized from these oligomers. The formation conditions exerted an influence over the molecular aggregation and the crystallization behaviors of the blend films and block copolymers which were examined by X-ray diffractometry and DSC analysis. As a result, phase-separation in the blend films was found when the formation temperature was high. The blend films formed at 340°C, quenched and annealed at 180°C, exhibited the same crystallization behavior as those of PEEK. In the case of the blend films formed at 300°C, the annealing of the films at 250°C was required to crystallize the blend films. The Tg of a copolymer with a PEEK component content of more than 50% tends to shift toward a higher temperature than the Tg of PEEK itself, and the Tm of the copolymer toward a lower temperature than that of PEEK ist. 相似文献
76.
Yoshitoshi Nakamura Tatsuro Sawada Akihiro Komatsu 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2002,77(10):1101-1106
In order to develop a method for converting raw starch into ethanol efficiently, direct fermentation of ozonized raw starch using a recombinant yeast was investigated. Ozonolysis was carried out as a pretreatment to convert raw starch into ethanol rapidly and efficiently, and then the effect of the ozone degradation conditions on the degree of polymerization and the amount of amylose in a raw starch was determined. Since the degree of polymerization was low and the amount of amylose was high, raw starch treated with an ozone concentration of 40 gm?3 and an ozonation time of 30 min was the material chosen for alcohol fermentation. Though the recombinant yeast could not convert the untreated raw starch, it converted the soluble starch and the ozonized raw starch at a comparatively high yield into ethanol. About 56% of the ozonized raw starch decomposed, and the ethanol concentration obtained from the ozonized raw starch was markedly greater than that obtained from untreated raw starch. The dynamic behavior of cell growth, substrate degradation, and ethanol production was examined in a continuous culture under various dilution rates, and the optimal dilution rate, ie 0.15 h?1, was determined for maximizing the ethanol productivity (amount of ethanol produced per unit time). © 2002 Society of Chemical Industry 相似文献
77.
Atsushi Takahashi Isao Nakamura Masaaki Haneda Tadahiro Fujitani Hideaki Hamada 《Catalysis Letters》2006,106(3-4):133-138
Catalytic hydrogenation of naphthalene to decalin was studied over a carbon-supported rhodium catalyst in supercritical carbon
dioxide solvent at 333 K, and the results were compared with those in an organic solvent. cis-, trans-Decalin and tetralin were formed from the beginning of the reaction in supercritical carbon dioxide. Higher concentration
of hydrogen in carbon dioxide solvent and on the active site, and also the suppression of desorption of partially hydrogenated
tetralin molecules from the active site would be responsible for higher selectivity to cis-decalin in supercritical carbon dioxide than that in an organic solvent. 相似文献
78.
Takashi Nakamura 《Lipids》1986,21(9):553-557
Prostaglandin-like substances other than 3-(2-ethyl-5-hydroxy-3-oxo)-cyclopentanyl-2-propenal (compound I), which upon reacting
with amino acids form reddish pigments, were purified, and their chemical structures were determined. Three red pigment-forming
substances (RPS) in autoxidized methyl linolenate were purified successively by gel chromatography on Sephadex LH-20, column
chromatography and thin layer chromatography on Silica Gel 60, and by high performance liquid chromatography on μ-Porasil.
IR spectra of the RPS showed the absorption of an ester group (νC=O 1730 cm−1 in CHCl3) and of a longer branched chain (νC-H 2800–3100 cm−1), in addition to the absorption bands observed in compound I. Electron impact mass spectra of the trimethylsilyl ethers obtained
after reduction with NaBH4 and NaBD4 were analyzed in detail and compared with those of compound I. The structures of the RPS were identified as stereoisomeric
methyl 8-[2-(2-formylvinyl)-3-hydroxy-5-oxo-cyclopentanyl]-octanoates derived from methyl 12-hydroperoxy-linolenate.
Presented at the general meeting of the Japanese Society of Scientific Fisheries, held at Tohoku University, Sendai, Japan,
October 1984. 相似文献
79.
Dimethylsiloxane-tetramethyl-p-silphenylenesiloxane-dimethylsiloxane (DMS-TMPS-DMS) triblock copolymer was synthesized by employing living anionic polymerization of hexamethylcyclotrisiloxane (D3). Two synthetic methods were carried out for the polymerization. One of those methods was the anionic polymerization of D3 initiated at the silanolate anion which was prepared from the terminal hydroxyl group of silanol-terminated TMPS prepolymer by reaction with n-butyllithium (method 1). The other was the coupling reaction of vinyl-terminated TMPS prepolymer with hydrosilyl-terminated DMS prepolymer obtained from the anionic polymerization of D3 by using diphenylmethylsilanolate anion as initiator (method 2). In method 1, DMS contents of the copolymers ranged from 25.8 to 72.5 wt% and the values agreed with the ratio of D3 to TMPS prepolymer. The weight-average molecular weights ranged from 1.36×104 to 19.4×104 and were close to the predicted values calculated from the of the TMPS prepolymer and the amount of D3 added. In the case of method 2, weight-average molecular weights ranged from 19.5×104 to 24.2×104. The high molecular weight copolymer could thus be obtained by method 2. Intrinsic viscosity values of the triblock copolymers agreed with calculated values obtained by considering the copolymer as a binary mixture of these homopolymers. Differential scanning calorimetry and thermogravimetry were carried out on the triblock copolymers. The equilibrium melting temperatures of each of the copolymers were very close to that of poly-TMPS (160°C). The glass transition temperature and heat of fusion were decreased as the DMS content was increased. The thermogravimetric curves for the copolymers indicated that the thermal stability of the triblock copolymer was intermediate between the DMS and TMPS homopolymers. 相似文献
80.
A technique for separating similar and diverse ionogenic mixtures into their individual homologs was studied by high performance
liquid chromatography on an octadecyl-silica (TSK Gel LS-410) column. Conditions used for the separation were: column size,
6 mm id×200 mm; mobile phase, water/methanol (15:85, v/v) containing (a) 1.0 M sodium perchlorate and adjsting to pH 2.5 with
phosphoric acid, (b) 0.1 M and pH 3.5; column temp., 50 C. By using 2 mobile phase conditions, various surfactant mixtures
were separated into their individual homologs and simultaneously distinguished from each other, regardless of their ionogenic
properties. 相似文献