全文获取类型
收费全文 | 4975篇 |
免费 | 385篇 |
国内免费 | 180篇 |
专业分类
电工技术 | 37篇 |
综合类 | 256篇 |
化学工业 | 3098篇 |
金属工艺 | 81篇 |
机械仪表 | 40篇 |
建筑科学 | 262篇 |
矿业工程 | 23篇 |
能源动力 | 70篇 |
轻工业 | 216篇 |
水利工程 | 16篇 |
石油天然气 | 158篇 |
武器工业 | 11篇 |
无线电 | 147篇 |
一般工业技术 | 1019篇 |
冶金工业 | 47篇 |
原子能技术 | 40篇 |
自动化技术 | 19篇 |
出版年
2024年 | 19篇 |
2023年 | 84篇 |
2022年 | 83篇 |
2021年 | 131篇 |
2020年 | 145篇 |
2019年 | 132篇 |
2018年 | 143篇 |
2017年 | 149篇 |
2016年 | 193篇 |
2015年 | 181篇 |
2014年 | 272篇 |
2013年 | 305篇 |
2012年 | 347篇 |
2011年 | 340篇 |
2010年 | 251篇 |
2009年 | 290篇 |
2008年 | 283篇 |
2007年 | 319篇 |
2006年 | 264篇 |
2005年 | 263篇 |
2004年 | 192篇 |
2003年 | 175篇 |
2002年 | 173篇 |
2001年 | 132篇 |
2000年 | 106篇 |
1999年 | 100篇 |
1998年 | 91篇 |
1997年 | 73篇 |
1996年 | 37篇 |
1995年 | 35篇 |
1994年 | 30篇 |
1993年 | 33篇 |
1992年 | 25篇 |
1991年 | 22篇 |
1990年 | 9篇 |
1989年 | 13篇 |
1988年 | 4篇 |
1987年 | 6篇 |
1986年 | 2篇 |
1985年 | 25篇 |
1984年 | 17篇 |
1983年 | 22篇 |
1982年 | 21篇 |
1981年 | 1篇 |
1951年 | 2篇 |
排序方式: 共有5540条查询结果,搜索用时 15 毫秒
1.
Oxidation behavior of a 2 mol % divinylbenzene (DVB)‐crosslinked polystyrene‐supported permanganate function was investigated toward low molecular weight primary and secondary alcohols and aldehydes. The permanganate function was attached to a polystyrene support through cyclic polyoxyethylene (POE) units immobilized on the support. Contrary to the oxidations catalyzed by low molecular weight permanganate reagents, the oxidation of primary alcohol terminated in the aldehyde stage. The secondary alcohols were converted to the respective ketone and aldehyde to acid. The effect of the variable parameters similar to solvent, temperature, and reagent to substrate ratio was followed. Nonpolar cyclohexane was found to be the best solvent for the present study. Also the reactivity increased with increasing temperature. The oxidizing reagent possesses a long shelf life and could be recycled several times without reduction of capacity and mechanical stability. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3708–3717, 2003 相似文献
2.
3.
P. Meenakshi S. E. Noorjahan R. Rajini U. Venkateswarlu C. Rose T. P. Sastry 《Bulletin of Materials Science》2002,25(1):25-29
DriedMusa paradiciaca (banana) stem and veins of the leaves, which were hitherto discarded as a waste, were collected and used as starting material
for the preparation of cellulose and cellulose acetate. This cellulose acetate was mixed with polystyrene to form blend of
cellulose acetate-polystyrene in order to provide enhanced stability and extended utility to the end products. The films of
these composites or their individual partners were made separately and studied for their mechanical properties, chemical modification
and morphological changes. We report here that banana stem is good source of cellulose and that cellulose completely undergoes
modification upon esterification. 相似文献
4.
Wei-Jun Liu Wei-Dong He Xue-Wu Ge Hua-Rong Liu Mo-Zheng Wang Zheng-Qi Chang 《Materials Letters》2007,61(13):2818-2821
Interfacial-initiated polymerization of styrene (St) was carried out in inversed emulsion with cumene hydroperoxide (CHPO) and ferrous sulfate (FeSO4)/disodium ethylenediaminetetraacetate (NaEDTA)/sodium formaldehyde sulfoxylate (SFS) as the redox initiation system. The water-soluble Fe2+-NaEDTA-SFS acted as the reducing component and the oil-soluble CHPO as the oxidant component of the redox initiation system. Therefore, the primary radicals were produced mainly at the oil/water interface to initiate the polymerization of St. Thus, sub-micrometer hollow polystyrene (PSt) spheres were obtained by one-stage polymerization, which was supported by the techniques of transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM). 相似文献
5.
Frdric Boschet Catherine Branger Andr Margaillan Thieo E Hogen‐Esch 《Polymer International》2005,54(1):90-95
The synthesis of 2,2,3,3‐tetrahydro‐perfluoroundecanoyl end‐functionalized polystyrene–poly(ethylene oxide) block (PS‐block‐PEO‐RF) copolymers and their matching PS‐block‐PEO diblock copolymers was carried out by sequential anionic polymerization. Viscometry and 19F NMR studies show that the PS‐block‐PEO copolymers, in contrast to their matching PS‐block‐PEO‐RF copolymers, exhibit a micellar rather than the associative behavior seen for the latter. However, the presence of an excess of fluorinated acid, used for end‐functionalization, produces a reduction of the associative behavior above the overlap concentration, with the fluorinated acid acting like a surfactant. A competition may also occur between PS—and RF—mediated micellization. Copyright © 2004 Society of Chemical Industry 相似文献
6.
Polystyrene‐fullerene compositions containing up to 0.45 mol % (3 wt %) fullerene C60 were investigated. It was established that the addition of fullerene to polystyrene (PS) leads to an increase of molecular packing density and so influences the transport of small molecules through the polymer films. Gas diffusion through films of PS‐fullerene compositions is slower than through PS films, and gas separating properties of compositions are higher. Dielectric studies showed that the fullerene is distributed as clusters in the polymer matrix of solid composition prepared from a toluene solution of PS and fullerene. Heating without air to the temperature higher than PS glass transition leads to increasing relaxation time of α‐transition in PS of compositions containing >0.15 mol % (1 wt %) fullerene. This effect is caused by rather strong interaction of PS chains via fullerene molecules entered into the PS‐fullerene complex. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2946–2951, 2002 相似文献
7.
P. Bocchetta C. Sunseri A. Bottino G. Capannelli G. Chiavarotti S. Piazza F. Di Quarto 《Journal of Applied Electrochemistry》2002,32(9):977-985
Alumina membranes were fabricated by anodizing aluminium metal in 0.15 M oxalic acid. The growth kinetics of the porous layer were investigated in the temperature range –1 to 16 °C using linear potential scans up to 70 V. The faradaic efficiencies of metal oxidation and of porous layer formation, determined by applying Faraday's law, were found to be independent of both temperature and electrical charge. SEM analysis of the metal-side and solution-side surfaces revealed different morphologies. After dissolution of the barrier layer in phosphoric acid, the metal-side surface showed circular pores whose size of about 90 nm was found to be uniform and independent of temperature. The pore population was also practically independent of temperature and a value of about 4 × 1013 pores m–2 was determined. On the solution-side surface the presence of a deposit partially occluding the mouths of pores was observed. This coating could be removed by chemical etching in NaOH or thermal treatment at 870 °C, where decomposition of oxalate occurs. This supports the hypothesis that the deposit consists of an aluminium salt containing oxalate anions precipitated from the solution. The results show that it is possible to control the morphological characteristics of the anodic alumina membranes by careful choice of experimental conditions. 相似文献
8.
Studies were made on the thermally stimulated discharge currents (TSDCs) in pure (undoped) and Fe-doped polystyrene films as a function of polarizing field, polarizing temperature and dopant concentration. While undoped films exhibited a single peak, doped films showed two peaks one at low temperatures and another at high temperatures. The low temperature peak, which exhibits a shift towards lower temperatures with increasing dopant concentration, is attributed to the relaxation of the main chain, while the high temperature peak, which shows a tendency to shift towards higher temperatures with dopant concentration, is due to space charge polarization. The TSDCs were higher for low dopant concentrations than their undoped counterparts, while for high concentrations of the dopant, the TSDCs decreased. Formation of charge transfer complexes at low dopant concentrations and molecular aggregates at higher dopant concentrations are suggested as the possible reasons for this behaviour. 相似文献
9.
Mohamed Jaziri Tasnim Kossentini Kallel Souad Mbarek Boubaker Elleuch 《Polymer International》2005,54(10):1384-1391
The influence of processing conditions and interfacial modification on the morphology evolution and the composition range within which fully co‐continuous high density polyethylene/polystyrene blend structures can exist during blending in a single screw extruder was studied. Blends ranging from pure A to pure B component, with and without compatibilizer, were prepared under two different shear rates. It was found that high shear rates displaced the breakdown–coalescence balance of the dispersed nodules to the side of coalescence, narrowing the percolation domain and the critical composition for full co‐continuity decreased with increasing shear rates. The addition of a tri‐block compatibilizer induced the percolation threshold of the polystyrene phase to begin at lower percentages of polyethylene but the phase inversion point did not change. The experimental results are discussed in the light of various theoretical models. Copyright © 2005 Society of Chemical Industry 相似文献
10.
Flame retardant and the degradation mechanism of high impact polystyrene/Fe-montmorillonite nanocomposites 总被引:1,自引:1,他引:0
High impact polystyrene/Fe-montmorillonite (HIPS/Fe-MMT) nanocomposites were successfully prepared by melting intercalation.
The nanostructures of HIPS/Fe-MMT were testified by X-ray diffraction (XRD) and transmission electron microscope (TEM). Corresponding
to pure HIPS, the thermal stability of HIPS/Fe-MMT nanocomposites was notably improved. The peaks of heat release rate (PHRR)
and the mass loss rate (MLR) were significantly reduced after the formation of the HIPS/Fe-MMT nanocomposites from cone calorimetry.
And nanocomposites PHRR was further lower with the increase of Fe-MMT content in the range of 1 to 5 wt%. The degradation
mechanism of HIPS and HIPS/Fe-MMT nanocomposites was conducted by pyrolysis gas chromatography mass spectrometry (Py-GC-MS).
And the reason of the enhancement of thermal stability maybe is that structural iron is the operative site for radical trapping
in the Fe-MMT and the nanostructure enhances the interaction of the chains of the HIPS. 相似文献