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51.
Tetsuo Sato Yasuhiro Takahata Takahiro Noda Takashi Yanagisawa Toshikazu Morishita Shinji Sakai 《Journal of the American Oil Chemists' Society》1995,72(10):1177-1183
Determination of the fatty acid composition of sunflower (Helianthus annua L.) seeds by near-infrared (NIR) spectroscopy was examined. Sunflower seeds were husked (removed from their hulls by a husking
machine or manually with a knife). NIR spectra of these seeds were scanned from 1100 to 2500 nm at 2-nm intervals in a whole-grain
cell with a wideangle moving drawer for machine-husked seeds or in a single-grain cup for a manually husked single-grain seed.
The extracted oils from machine-husked seeds also were scanned by sandwiching them between a pair of slide glasses to create
a thin layer and by placing them on a syrup cup. For extracted oil, the absorption band around 1720 nm filled out to the shorter
wavelength region in the NIR second-derivative spectra as the percentage of the linoleic acid moiety increased, because linoleic
acid absorbs in this region. On the other hand, for husked seeds and for a single-grain seed, as the percentage of linoleic
acid increased, the trough at 1724 nm where oleic and saturated acids absorb decreased in the second-derivative NIR spectra.
Determination of the fatty acid composition of sunflower seeds could be carried out successfully according to the NIR spectral
pattern for both extracted oil (r=−0.989) and kernel seed (r=−0.993). This is important, especially for a manually husked
single-grain seed (r=−0.971), because it can still be germinated after such nondestructive analysis. 相似文献
52.
Selectivity and mechanism for skeletal isomerization of alkanes over typical solid acids and their Pt-promoted catalysts 总被引:2,自引:0,他引:2
Atsuyuki Miyaji Tsuneo Echizen Lianshun Li Tetsuo Suzuki Yusuke Yoshinaga Toshio Okuhara 《Catalysis Today》2002,74(3-4):291-297
Selectivities for skeletal isomerizations of n-butane and n-pentane catalyzed by typical solid acids such as Cs2.5H0.5PW12O40 (Cs2.5), SO42−/ZrO2, WO3/ZrO2, and H-ZSM-5 and their Pt-promoted catalysts were compared. High selectivities for n-butane and low selectivity for n-pentane were observed over Cs2.5 and SO42−/ZrO2, while H-ZSM-5 was much less selective, and WO3/ZrO2 was highly selective for both reactions. The Pt-promoted solid acids were usually selective for these reactions in the presence of H2 except for Pt-H-ZSM-5 for n-butane isomerization. Both the acid strength and pore structure would be factors influencing the selectivity. Mechanism of skeletal isomerization of n-butane was investigated by using 1,4-13C2-n-butane over Cs2.5 and Pt–Cs2.5. It was concluded that n-butane isomerization proceeded mainly via monomolecular pathway with intramolecular rearrangement on Pt–Cs2.5, while it occurred through bimolecular pathway with intermolecular rearrangement on Cs2.5. The higher selectivity on Pt–Cs2.5 would be brought about by the monomolecular mechanism. In the skeletal isomerization of cyclohexane, Pt–Cs2.5/SiO2 was highly active and selective, while Pt–Cs2.5 was less selective. Control in the acid strength of Cs2.5 by the supporting would be responsible for the high selectivity. 相似文献
53.
Tetsuo Asakura Motohiro Kitaguchi Makoto Demura Harutoshi Sakai Keiichi Komatsu 《应用聚合物科学杂志》1992,46(1):49-53
The enzyme glucose oxidase (GOD) was immobilized on the nonwoven fabrics, which have excellent properties in diffusivity of substrates, mechanical strength, and handling, with Bombyx mori silk fibroin gel. The nonwoven fabrics of silk fibroin, viscose rayon, poly-ethyleneterephthalate, 6-nylon, and polypropylene with activated surface by fluoline treatment were used. The stabilities of GOD to heat or pH changes were much improved by the immobilization as well as the case of the GOD immobilized in the silk fibroin membrane. Among nonwoven fabrics, silk fibroin was the most excellent support material for the immobilization of GOD although all nonwoven fabrics used here are able to be used as the support materials. The increase of the sensitivity was observed when the glucose sensor was made with the GOD immobilized on nonwoven silk fabrics as four times compared with the case of the GOD immobilized in the silk fibroin membrane. 相似文献
54.
Yusaku Takita Jun-ichi Moriyama Hiroyasu Nishiguchi Tatsumi Ishihara Fusakazu Hayano Tetsuo Nakajo 《Catalysis Today》2004,88(3-4):103-109
Activity for hydrolysis of CCl2F2 (CFC12) on various metal sulfate was investigated. Zr(SO4)2 was found to be the most active while FeSO4, Cr2(SO4)3, Al2(SO4)3, La2(SO4)3 and Ce2(SO4)3 had intermediate activity. MnSO4, CoSO4, and MgSO4 showed low activity and SrSO4, CaSO4, and BaSO4 had even less activity. The major carbon containing product was CO2 and small amount of CClF3 and CO were formed over several sulfates. The crystal structure of the sulfates was stable during decomposition of CCl2F2, and the conversion reached a steady state after initial decrease at 275 °C over Zr(SO4)2 catalyst. The concentration of surface hydroxyl was larger than that over AlPO4-based catalysts and a reaction mechanism similar to that over AlPO4-based catalysts was proposed. 相似文献
55.
Hiromi Yoshida Yuka Tomiyama Masayuki Saiki Yoshiyuki Mizushina 《Journal of the American Oil Chemists' Society》2007,84(11):1031-1038
The positional distribution of fatty acids (FA) of triacylglycerols (TAG) and major phospholipids (PL) prepared from four
cultivars of peas (Pisum sativum L.) were investigated as well as their tocopherol contents. The lipids extracted from these peas were separated by thin-layer
chromatography (TLC) into seven fractions. The major lipid components were PL (52.2–61.3%) and TAG (31.2–40.3%), while the
other components were also present in minor proportions (5.6–9.2%). γ-Tocopherol was present in the highest concentration,
and α- and δ-tocopherols were very small amounts. The main PL components isolated from the four cultivars were phosphatidylcholine
(42.3–49.2%), followed by phosphatidylinositol (23.3–25.2%) and then phosphatidylethanolamine (17.7–20.5%). Small but significant
differences (P < 0.05) in FA distribution existed when different pea cultivars were determined. However, the principal characteristics of
the FA distribution in the TAG and the three PL were evident among the four cultivars; unsaturated FA were predominantly located
in the sn-2 position, and saturated FA primary occupied the sn-1 or sn-3 position in the oils of the peas. These results suggest that the regional distribution of tocopherols and fatty acids in
peas is not dependent on the climatic conditions and the soil characteristics of the cultivation areas during the growing
season. 相似文献
56.
57.
58.
Tohru S. Suzuki Tetsuo Uchikoshi Yoshio Sakka 《Journal of the European Ceramic Society》2009,29(12):2627-2633
The preparation of oriented AlN bulk ceramics with and without additives was achieved by slip casting in a high magnetic field. The a and b axes of the AlN were aligned parallel to the direction of the magnetic field. The degree of crystallographic orientation was controlled by the viscosity of the slurry and the grain growth during sintering attributed to the sintering additives. The mechanical properties of the textured AlN depended on the direction of the crystallographic orientation. 相似文献
59.
Takuji Yamamoto Tomofumi Nishimura Tetsuo Suzuki Hajime Tamon 《Drying Technology》2001,19(7):1319-1333
Resorcinol-formaldehyde hydrogels were synthesized by sol-gel polycondensation of resorcinol with formaldehyde in a slightly basic aqueous solution. RF cryogels, RF xerogels, and RF xerogels (MW gels) were respectively prepared from RF hydrogels by freeze drying, hot air drying, and microwave drying. Carbon cryogels, carbon xerogels and carbon MW gels were subsequently obtained by pyrolyzing RF drygels in an inert atmosphere. Freeze drying and microwave drying were effective to prepare mesoporous RF drygels and carbon gels. RF cryogels and carbon cryogels showed high mesoporosity over wide ranges of the molar ratio of resorcinol to catalyst (R/C) and the ratio of resorcinol to water (R/W) used in sol-gel polycondensation. Although RF xerogels had a few mesopores, carbon xerogels had no mesopores. RF MW gels and carbon MW gels showed mesoporosity if appropriate values of R/C and R/W were selected. 相似文献
60.
Masahiro Nagae Tetsuo Yoshio Yoshito Takemoto Jun Takada 《Journal of the American Ceramic Society》2001,84(5):1175-1177
For pure molybdenum nitrided at 1373 K in NH3 gas, microstructural observations of a molybdenum nitride layer were conducted through a transmission electron microscope. The molybdenum nitride layer consisted of two molybdenum nitrides: an outer one of γ-Mo2 N and an inner one of β-Mo2 N. A great number of (011)[0 1] type twins were observed in the β-Mo2 N phase, whereas the microstructure of the γ-Mo2 N phase was almost free from lattice defects except for slightly observed {111}〈112〉 type twin. 相似文献