全文获取类型
收费全文 | 5107篇 |
免费 | 185篇 |
国内免费 | 20篇 |
专业分类
电工技术 | 327篇 |
综合类 | 15篇 |
化学工业 | 1500篇 |
金属工艺 | 139篇 |
机械仪表 | 148篇 |
建筑科学 | 125篇 |
矿业工程 | 5篇 |
能源动力 | 228篇 |
轻工业 | 428篇 |
水利工程 | 18篇 |
石油天然气 | 6篇 |
无线电 | 379篇 |
一般工业技术 | 1013篇 |
冶金工业 | 379篇 |
原子能技术 | 142篇 |
自动化技术 | 460篇 |
出版年
2023年 | 32篇 |
2022年 | 11篇 |
2021年 | 134篇 |
2020年 | 62篇 |
2019年 | 78篇 |
2018年 | 91篇 |
2017年 | 76篇 |
2016年 | 125篇 |
2015年 | 89篇 |
2014年 | 140篇 |
2013年 | 275篇 |
2012年 | 274篇 |
2011年 | 316篇 |
2010年 | 261篇 |
2009年 | 292篇 |
2008年 | 311篇 |
2007年 | 241篇 |
2006年 | 235篇 |
2005年 | 166篇 |
2004年 | 166篇 |
2003年 | 188篇 |
2002年 | 163篇 |
2001年 | 88篇 |
2000年 | 95篇 |
1999年 | 81篇 |
1998年 | 177篇 |
1997年 | 129篇 |
1996年 | 109篇 |
1995年 | 97篇 |
1994年 | 84篇 |
1993年 | 83篇 |
1992年 | 64篇 |
1991年 | 64篇 |
1990年 | 43篇 |
1989年 | 54篇 |
1988年 | 19篇 |
1987年 | 43篇 |
1986年 | 25篇 |
1985年 | 48篇 |
1984年 | 24篇 |
1983年 | 37篇 |
1982年 | 34篇 |
1981年 | 34篇 |
1980年 | 20篇 |
1979年 | 25篇 |
1978年 | 25篇 |
1977年 | 22篇 |
1976年 | 18篇 |
1975年 | 10篇 |
1974年 | 9篇 |
排序方式: 共有5312条查询结果,搜索用时 406 毫秒
101.
Yasushi Endo Sanae Hoshizaki Kenshiro Fujimoto 《Journal of the American Oil Chemists' Society》1997,74(9):1041-1045
Thirteen synthetic triacylglycerols (TAG) containing eicosapentaenoic acid (EPA) or docosahexaenoic acid (DHA) were oxidized
in the presence of 2,2′-azobis(2,4-dimethyl-valeronitrile) (AMVN) and 2,2′-azobis(2-amidinopropane)dihydrochloride (AAPH)
as aqueous and nonaqueous radical initiators to investigate the influence of TAG structure and oxidation system on the oxidative
stability of TAG that contain highly unsaturated fatty acids (HUFA). A 2:1 (mol/mol) mixture of trieicosapentaenoylglycerol
and tripalmitoylglycerol was most susceptible to the AMVN-initiated oxidation among three types of TAG that contained EPA
and palmitic acid (2:1, mol/mol). Compared with 1,2 (or 2,3)-dieicosapentaenoyl-3(or 1)-palmitoylglycerol (EEP) and 1,3-dieicosapentaenoyl-2-palmitoylglycerol
(EPE), the oxidative rate of EEP was somewhat higher. A similar result was obtained for DHA-containing TAG. The oxidative
rate of TAG that contained EPA and palmitic acid (1:2, mol/mol) showed a positive correlation with the amount of EPA in a
single TAG molecule. Moreover, in the nonaqueous system, the oxidative rate of EPA-containing TAG was affected by unsaturation
and carbon chainlength of constituent fatty acids. In the AAPH-initiated oxidation in the aqueous system, the oxidative rate
of TAG with EPA and palmitic acid was higher with the increased quantity of EPA in a single TAG molecule. Also, constituent
fatty acids modified the oxidative rate of EPA-containing TAG in an aqueous system. The glycerol position of EPA and DHA also
affected the oxidative rate of the TAG. EPA and DHA located at the 1,2 (or 2,3)-position of glycerol were more oxidizable
than those at the 1,3-position during AAPH-initiated oxidation. Thus, 1,2(or2,3)-dipalmitoyl-3(or 1)-eicosapentaenoylglycerol
was oxidized faster than 1,3-dipalmitoyl-2-eicosapentaenoylglycerol. These observations suggest that the oxidative stability
of TAG that contain HUFA could be modulated by the oxidation system and TAG structure. 相似文献
102.
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
103.
Noboru Hashimoto Yasushi Sawada Takashi Bando Hiroyoshi Yoden Shigehito Deki 《Journal of the American Ceramic Society》1991,74(6):1282-1286
AIN powder was synthesized from aluminum polynuclear complexes. Basic aluminum chloride and basic aluminum lactate were used as the aluminum polynuclear complexes. These starting materials and glucose were dissolved in water and mixed homogeneously. AIN powder was obtained by calcining after drying and precalcining at 800°C under nitrogen gas flow. Then excess carbon was removed by firing in air. Nitridation in the system was investigated and compared with that in the alumina–carbon black system. It was found that in our reaction system nitridation began and proceeded at lower calcination temperatures above 1200°C than in the alumina–carbon black system. Using aluminum polynuclear complexes, AIN was synthesized through the nitridation of γ-alumina and produced in a very fine and sharp particle size distribution. 相似文献
104.
This paper presents a new maritime lifesaving multiple-effect solar still design where several extended wicks feed seawater to their evaporating areas by capillary force, and the resulting water vapor diffuses and condenses on facing wicks with the condensate flowing through the wicks into storage bags. A theoretical analysis showed that a temperature drop through diffusion layers between evaporating and condensing wicks slowly increases in the main evaporating areas and rapidly near salt depositions whereas the evaporation rate decreases slowly in the main area and rapidly near salt depositions. These changes are caused by increases in salt concentrations and resulting boiling point elevation. With steady-state transfer analysis, the proposed still is predicted to produce about 15 kg m −2d−1 fresh water on a sunny day of 22 MJm−2d−1 solar radiation, showing a potential to be a maritime lifesaving desalinator. 相似文献
105.
Uphill transport of ammonium ions through a membrane with sulfonic acid groups were investigated with pH-controllers which keep the solution at a constant pH. A membrane with sulfonic acid groups was prepared by casting an aqueous solution containing poly(styrenesulfonic acid) and poly(vinyl alcohol) on a glass plate. When a membrane with one side alkaline and the other acidic was fixed as a diaphragm in a cell, ammonium ions were transported from the alkaline side to the acidic side through the membrane against the concentration gradient of the adjacent solutions. Uphill transport of ammonium ions with pH-controllers was more efficient than without, thus keeping the pH difference between both sides of the membrane constant, which is a driving force for the uphill transport. Furthermore, the effect of pH of the acidic side on the uphill transport was investigated and the mechanism of the pH-controlled uphill transport is discussed. 相似文献
106.
Because of their unique structures and properties, π-conjugated polymers have attracted the attention of scientists and engineers. The authors have studied the synthesis of two kinds of π-conjugated poly(aromatic acetylene)s, i.e. poly(arylacetylene)s and poly(aryleneethynylene)s with the aim of obtaining new polymers having novel functions or higher performances. This review mainly concerns the authors' results, as follows: first, we describe the synthesis and properties of achiral poly(arylacetylene)s, containing trimethylsilyl groups, oligodimethylsiloxanyl groups, dendritic groups, and glavinoxyl groups, for application as oxygen permselective membrane materials. Their self-membrane-forming abilities and high oxygen permeabilities are presented. Second, the synthesis by asymmetric-induced polymerization of chiral poly(arylacetylene)s having both a main-chain chirality and chiral pendant groups and their application as optical resolution membranes are described. Third, two new synthetic methods for preparing chiral helical poly(phenylacetylene)s without the coexistence of any other chiral moieties are presented. One is helix-sense-selective addition polymerization and the other is in situ removal of chiral pendant groups from membranes of poly(arylacetylene)s that also contain a main-chain chirality. The chiral helical poly(arylacetylene)s were tested as optical resolution membranes. The chiral and achiral poly(arylacetylene)s were synthesized by addition polymerization using metathesis catalysts or rhodium complexes. Finally, the synthesis of regiospecific poly(aryleneethynylene)s bearing stable radicals by the polycondensation of bromoethynylanthracene derivatives using a Pd(0) complex is described. The magnetization and the static magnetic susceptibility of the polyradicals are explained. 相似文献
107.
Hidehiko Kobayashi Kenichi Shimosaka Miki Saitoh Takashi Mitamura 《Journal of the American Ceramic Society》1993,76(9):2389-2392
We investigated the conditions for low-temperature synthesis of ZrC fine powder from ZrO2 –Mg–CH4 . The synthesis utilizes a thermite-type reaction, with Mg as the reducing agent, and a reaction between Mg and CH4 gas as a carbon source. The Mg/ZrO2 molar ratio as well as the heating rate were varied. Because C can be continuously fed into the reaction group by the cyclic reaction of Mg through the formation and decomposition of Mg2 C3 (2Mg + 3CH4 → Mg2 C3 + 6H2 → 2Mg + 3C), a molar ratio of 2.2 for Mg/ZrO2 was sufficient for the synthesis of single-phase ZrC. ZrC powders were synthesized under the following conditions: Mg/ZrO2 molar ratio = 2.2, heating rate = 20°C/min, and temperature maintained at 750°C for 30 min. The amount of reaction heat produced in the reduction reaction of ZrO2 by Mg depended on the Mg/ZrO2 molar ratio, specifically, the amount of ZrO2 contained. Moreover, the cyclic reaction of Mg-Mg2 C3 –Mg was influenced by the amount of reaction heat described above and by the heating rate. The ZrC fine powder showed little aggregation and high dispersibility. 相似文献
108.
Takashi Yamashiki Toshihiko Matsui Keisuke Kowsaka Masayoshi Saitoh Kunihiko Okajima Kenji Kamide 《应用聚合物科学杂志》1992,44(4):691-698
A novel cellulose solution, prepared by dissolving an alkali-soluble cellulose, which was obtained by the steam explosion treatment on almost pure natural cellulose (soft wood pulp), into the aqueous sodium hydroxide solution with specific concentration (9.1 wt %) was employed for the first time to prepare a new class of multifilament-type cellulose fiber. For this purpose a wet spinning system with acid coagulation bath was applied. The mechanical properties and structural characteristics of the resulting cellulose fibers were compared with those of regenerated cellulose fibers such as viscose rayon and cuprammonium rayon commercially available. X-ray analysis shows that the new cellulose fiber is crystallographically cellulose II, and its crystallinity is higher but its crystalline orientation is slightly lower than those of other commercial regenerated fibers. The degree of breakdown of intramolecular hydrogen bond at C3[Xam(C3)] of the cellulose fiber, as determined by solid-state cross-polarization magic-angle sample spinning (CP/MAS) 13C NMR, is much lower than other, and the NMR spectra of its dry and wet state were significantly different from each other, indicating that cellulose molecules in the new cellulose fiber are quite mobile when wet. This phenomenon has not been reported for so-called regenerated cellulose fibers. 相似文献
109.
Lida T Nakamori R Yabuta R Yada S Takagi Y Mano N Ikegawa S Goto J Nambara T 《Lipids》2002,37(1):101-110
A facile and efficient synthesis of the carboxyl-linked glucosides of bile acids is described. Direct esterification of unprotected
bile acids with 2,3,4,6-tetra-O-benzyl-d-glucopyranose in pyridine in the presence of 2-chloro-1,3,5-trinitrobenzene as a coupling agent afforded a mixture of the
α- and β-anomers (ca. 1∶3) of the 1-O-acyl-d-glucoside benzyl ethers of bile acids, which was separated effectively on a C18 reversedphase chromatography column (isolated yields of α- and β-anomers are 4–9% and 12–19%, respectively). Subsequent hydrogenolysis
of the α- and β-acyl glucoside benzyl ethers on a 10% Pd−C catalyst in acetic acid/methanol/EtOAc (1∶2∶2, by vol) at 35°C
under atmospheric pressure gave the corresponding free esters in good yields (79–89%). Chemical specificities such as facile
hydrolysis and transesterification of the acyl glucosides in various solvents were also discussed. 相似文献
110.
The glass transition behavior of emulsion-polymerized poly(methyl methacrylate) and polystyrene films containing sodium laurylsulfate as emulsifier was studied by measurements of dynamic mechanical properties and thermal depolarization current. The film specimens of the emulsion-polymerized polymers were prepared by casting from their benzene solutions. The glass transition temperatures of the emulsion-polymerized films are higher than those of the bulk-polymerized films. The higher glass transition temperature of the emulsion-polymerized films is attributed to the colloidal properties of sodium laurylsulfate in the process of the film formation. The restriction of the molecular chains in the emulsion-polymerized films is attributed to the interaction between the hydrophobic groups of sodium laurylsulfate and the polymer molecules. 相似文献