全文获取类型
收费全文 | 2081篇 |
免费 | 40篇 |
国内免费 | 6篇 |
专业分类
电工技术 | 84篇 |
综合类 | 1篇 |
化学工业 | 405篇 |
金属工艺 | 68篇 |
机械仪表 | 37篇 |
建筑科学 | 33篇 |
能源动力 | 36篇 |
轻工业 | 127篇 |
水利工程 | 4篇 |
无线电 | 206篇 |
一般工业技术 | 305篇 |
冶金工业 | 632篇 |
原子能技术 | 50篇 |
自动化技术 | 139篇 |
出版年
2023年 | 14篇 |
2022年 | 29篇 |
2021年 | 24篇 |
2020年 | 8篇 |
2019年 | 19篇 |
2018年 | 27篇 |
2017年 | 27篇 |
2016年 | 30篇 |
2015年 | 17篇 |
2014年 | 33篇 |
2013年 | 63篇 |
2012年 | 54篇 |
2011年 | 92篇 |
2010年 | 49篇 |
2009年 | 63篇 |
2008年 | 59篇 |
2007年 | 62篇 |
2006年 | 41篇 |
2005年 | 54篇 |
2004年 | 53篇 |
2003年 | 52篇 |
2002年 | 51篇 |
2001年 | 45篇 |
2000年 | 45篇 |
1999年 | 67篇 |
1998年 | 265篇 |
1997年 | 151篇 |
1996年 | 109篇 |
1995年 | 62篇 |
1994年 | 48篇 |
1993年 | 47篇 |
1992年 | 29篇 |
1991年 | 33篇 |
1990年 | 24篇 |
1989年 | 23篇 |
1988年 | 15篇 |
1987年 | 16篇 |
1986年 | 13篇 |
1985年 | 20篇 |
1984年 | 10篇 |
1983年 | 20篇 |
1982年 | 11篇 |
1981年 | 20篇 |
1980年 | 16篇 |
1979年 | 7篇 |
1978年 | 11篇 |
1977年 | 23篇 |
1976年 | 27篇 |
1974年 | 9篇 |
1973年 | 7篇 |
排序方式: 共有2127条查询结果,搜索用时 0 毫秒
41.
We examined the influence of polyaniline (PAn)'s unit sequence and doping with low molecular weight dopants or polymer dopants on permeation property. It was found that CO2 permeability was increased by the formation of a quinonediimine unit in PAn with the oxidation. CO2 sorption amount of PAn was decreased by oxidation. The increase of CO2 permeability with oxidation, therefore, resulted from the increase of diffusivity, which was attributable to morphological variation by the increase of a quinonediimine unit. The permselectivity of PAn films was found to be remarkably improved by doping. In particular, the selectivity value of the PAn film doped with polyvinyl sulphonic acid as a polymer dopant went up to over 2,000. This remarkable increase of selectivity was found to result in the increase of selectivity, depending on diffusivity. It was also found that the permselectivity of the PAn film doped by polymer dopants was surpassed, as compared with that doped by low molecular dopants. © 1995 John Wiley & Sons, Inc. 相似文献
42.
An investigation was undertaken on the application of dilute chitosan solutions gelled by tyrosinase‐catalyzed reaction with 3,4‐dihydroxyphenethylamine (dopamine). The tyrosinase‐catalyzed reaction with dopamine conferred water‐resistant adhesive properties to the semidilute chitosan solutions. The viscosity of the chitosan solutions increased highly by the tyrosinase‐catalyzed reaction and the subsequent reactions between o‐quinone compounds and chitosan. These highly viscous, gel‐like modified chitosan materials were allowed to spread onto the surfaces of the glass slides, which were tightly lapped together and held them in water. Tensile shear adhesive strength of over 400 kPa was observed for the modified chitosan samples. The increase in the amino group concentration of the chitosan solutions and the molecular mass of the chitosan used effectively led to the increase in adhesive strength of the glass slides. In addition, in the case where the chitosan solution was gelled by the enzymatic reaction with dopamine in the presence of poly(ethylene glycol), adhesive strength sharply increased at shorter reaction times concomitantly with the increase in the viscosity of the chitosan solutions because the tyrosinase activity effectively was retained by poly(ethylene glycol). © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1818–1827, 2007 相似文献
43.
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
44.
The characteristics of gas bubbles in a 5 cm diameter bubble column equipped with a single orifice of 1,3 or 5 mm diameter were investigated under system pressure of 0.1-15 MPa. The formation of gas bubbles was strongly affected by the system pressure. Under high pressures a dispersed gas jet was formed at gas velocities where spherical gas bubbles would have been formed at atmospheric pressure. The critical gas velocity between the bubbling regime and the jetting regime was correlated with the liquid phase Weber number and the gas phase Reynolds number based on the gas velocity at the orifice. Bubble size and gas holdup in the main part of the bubble column were also affected by the bubble formation pattern at the distributor 相似文献
45.
Summary Several metal oxides-supported TiCl3 catalysts were prepared and propylene polymerization was conducted over them without cocatalysts. It was found that isotactic polymerization of propylene took place effectively over them. 相似文献
46.
Summary It was found that isotactic polymerization of propylene took place over titanium ion-exchanged Y-zeolite without organometallic compounds. The results obtained have led to the conclusions that Ti4+ species as well as Ti3+ species are active for the polymerization and that neither Ti-alkyl bonds nor Cl ligands are necessarily essential for polymerization of propylene. 相似文献
47.
The liver lipogenic enzymes are compared among rats, chickens, frogs and fish. Although the apparent Km values of glucose-6-phosphate
dehydrogenase for glucose-6-phosphate are not much different among all the species, those of malic enzyme for malate are much
higher in chickens and fish than in rats and frogs. Glucose-6-phosphate dehydrogenase showed very high activities compared
with malic enzyme in fish liver, and malic enzyme showed high activities in chicken liver. Although the apparent Km values
of acetyl-CoA carboxylase and fatty acid synthetase for substrates are in the same range among all the animals, the activity
of acetyl-CoA carboxylase seems to be extremely low in fish and frog livers, and that of fatty acid synthetase is low in frog
livers only. In addition, the apparent Km values of α-glycerophosphate acyltransferase of fish liver are very high, and the
enzyme activity appears to be extremely low compared to the others. Therefore, the enzymes at the first steps of both fatty
acid and glycerolipid syntheses of poikilothermos animals appear to be very low. On the other hand, the Ouchterlony double-diffusion
patterns showed that the lipogenic enzymes of chickens, frogs and fish are immunologically different from those of rats, with
the exception of acetyl-CoA carboxylase in chickens. Therefore, it is suggested that the fatty acid and glycerolipid forming
systems of poikilothermos animals are quite different from those of homoiothermos and the lipogenesis is very low in poikilothermos. 相似文献
48.
The prooxidant property of inorganic chromium compounds was determined in methyl linoleate free from natural antioxidants
and metals. Prooxidant properties of inorganic chromium compounds appeared in order of sodium chromate > chromium (VI)-oxide
> chromium chloride > potassium chromate > chromium (III)-oxide > potassium dichomate. In comparison with the control, additions
of chromium compounds induced different amounts of autoxidation products derived from methyl linoleate, such as small amounts
of hydroperoxides and conjugated dienes and large amounts of hydroxy groups,α,β,γ,δ-unsaturated carbonyls, isolatedtrans double bonds, polymers, and free radicals. From these analytical data, the catalysis of chromium compounds in the autoxidation
of methyl linoleate seemed to be based on their abilities of abstracting a hydrogen from methyl linoleate and decomposing
hydroperoxides derived from the autoxidation of methyl linoleate. 相似文献
49.
Various polymeric phosphonium salts containing long alkyl chains (C10? C18) and their corresponding model compounds were prepared, which possess the same hydrophobic structure as that of the common disinfectants (quaternary ammonium salts), and their antibacterial activities were evaluated by means of the viable cell counting method against Staphylococcus aureus (Gram-positive) and Escherichia coli (Gram-negative). The polymer with the decyl group exhibited a higher activity than that of the corresponding model compound, particularly against the Gram-positive strain. Furthermore, antibacterial activity of the polymers was found to decrease as the chain length increased. In contrast with the polymers, the antibacterial activity of the corresponding model compounds increased as hydrophobicity of the substituents increased. The antibacterial activity was strongly dependent on the structure, particularly on the length of the alkyl chain. © 1994 John Wiley & Sons, Inc. 相似文献
50.
Masanori Yamazaki Akiko Nishijima Kazuko Ikeda Shoji Ichihara 《Polymer Bulletin》2004,52(3-4):267-274
Summary
In order to obtain materials with nanopores which will be applicable for many fields, the structures of the cured blends of phenolic resin (PhN), poly(methyl methacrylate) (PMMA) and curing agent were studied. After PMMA was extracted from cured blends, the structures of cured phenolic resins were observed with SEM. As a results, it was found that nanosized continuous pore structures were formed in extremely wide composition region if curing temperature was high. 相似文献