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31.
The thermophysical properties of three kinds of fruit juices (grape juice, orange juice, and pineapple juice) were measured at various temperatures (10–50 °C) and concentrations (10–50%). A new method for the simultaneous determination of thermophysical properties using a modified version of current probe theory method was proposed. The temperature changes of the probe upon insertion in the sample were fitted to an approximate solution of the heat conduction equation, and the values of two parameters in that solution were determined. Using the values of these parameters, the thermal conductivity and thermal diffusivity of each sample were determined. The specific heat of each sample was estimated from the definition of thermal diffusivity. These thermophysical properties were expressed as a function of concentration and temperature. 相似文献
32.
Yen‐Ting Lin Ting‐Wei Yeh Yoshitake Nakajima P. Daniel Dapkus 《Advanced functional materials》2014,24(21):3162-3171
GaN nanorod formation on Ga‐polar GaN by continuous mode metalorganic chemical vapor deposition selective area growth (MOCVD SAG) is achieved under a relatively Ga‐rich condition. The Ga‐rich condition, provided by applying a very low V/III ratio, alters the growth rates of various planes of the defined nanostructure by increasing relative growth rate of the semi‐polar tilted m‐plane {1–101} that usually is the slowest growing plane under continuous growth conditions. This increased growth rate relative to the non‐polar m‐plane {1–100} and even the c‐plane (0001), permits the formation of GaN nanorods with nonpolar sidewalls. In addition, a new growth mode, called the NH3‐pulsed mode, is introduced, utilizing the advantages of both the continuous mode and the lower growth rate pulsed mode to form nanorods. Finally, nanorods grown under the different growth modes are compared and discussed. 相似文献
33.
Sausan Al-Riyami Shinya Ohmagari Tsuyoshi Yoshitake 《Diamond and Related Materials》2010,19(5-6):510-513
Nitrogen-doped ultrananocrystalline diamond (UNCD)/hydrogenated amorphous carbon (a-C:H) films were deposited by pulsed laser deposition (PLD). Nitrogen contents in the films were controlled by varying a ratio in the inflow amount between nitrogen and hydrogen gases. The film doped with a nitrogen content of 7.9 at.% possessed n-type conduction with an electrical conductivity of 18 Ω? 1 cm? 1 at 300 K. X-ray photoemission spectra, which were measured using synchrotron radiation, were decomposed into four component spectra due to sp2, sp3 hybridized carbons, C=N and C–N. A full-width at half-maximum of the sp3 peak was 0.91 eV. This small value is specific to UNCD/a-C:H films. The sp2/(sp3 + sp2) value was enhanced from 32 to 40% with an increase in the nitrogen content from 0 to 7.9 at.%. This increment probably originates from the nitrogen incorporation into an a-C:H matrix and grain boundaries of UNCD crystallites. Since an electrical conductivity of a-C:H does not dramatically enhance for this doping amount according to previous reports, we believe that the electrical conductivity enhancement is predominantly due to the nitrogen incorporation into grain boundaries. 相似文献
34.
Maeda Yoshitake; Koga Hiroshi; Yamada Hidenori; Ueda Tadashi; Imoto Taiji 《Protein engineering, design & selection : PEDS》1995,8(2):201-205
To increase the folding yield of concentrated reduced lysozyme,we developed a renaturation method by means of dialysis fromconcentrated urea with redox agents. After lysozyme was incubatedin the reducing buffer (8 M urea solution) with oxidized glutathione,renaturation of reduced lysozyme was started by dialysis againstthe dialyzing buffer containing 8 M urea with redox agents.The urea concentration of the dialyzing bottle was graduallydiluted with dialyzing buffer without urea at a flow rate of0.1 ml/min by high pressure pump. Using this systematic dialysis,a concentration as high as 5 mg/ml of reduced lysozyme couldbe renaturated in 80% yield, while the folding yield was <5%even at a concentration of 1 mg/ml using a conventional rapiddilution method [Goldberg et al. (1991) Biochemistry, 30, 27902797].Therefore, it was concluded that gentle removal of urea fromdenatured proteins, dissolved in concentrated urea solution,by means of dialysis should be useful to renature denaturedproteins effectively. 相似文献
35.
Kojiro Nakai Yasunori Oumi Haruyuki Horie Tsuneji Sano Hideaki Yoshitake 《Microporous and mesoporous materials》2007,100(1-3):328-339
Bromination and subsequent ethylenediamine substitution of the CC double bond in mesoporous ethylenesilica were carried out to explore the characteristics of this periodic mesoporous organosilica. The structures of the products (BrPMO and EDA–BrPMO, respectively) were analysed by IR, Br K-edge EXAFS and NMR spectroscopies, as well as X-ray diffraction and nitrogen adsorption. We showed (1) that the formulae of the two products that formed were [CHBrSiO1.5]0.45[CHSiO1.5]0.55 and [NH2CH2CH2NHCHSiO1.5]0.05 [CHBrSiO1.5]0.40[CHSiO1.5]0.55, respectively, (2) that the addition of Br2 at room temperature occurred on the CC double bonds with disturbing the framework structure, (3) that IR absorption band of CC bonds that reacted with Br2 is significantly different from that of inactive CC bond, (4) that the length of the C–Br bond was considerably longer than in conventional alkyl bromides, and (5) that a large proportion of the ν(C–Br) band remained at the same position in the IR absorption spectrum after the ethylenediamine (EDA) substitution, while a new ν(C–Br) absorption also appeared. The mechanisms of these reactions are discussed at both the micro and mesoscopic levels.
Arsenate adsorption on EDA–BrPMO, in which the EDA is directly bound to the “surface” of the mesopores, was compared with adsorption on EDA–Pr–PMO, which was prepared by the direct synthesis of 3-chloropropyl-functionalized mesoporous ethanesilica followed by the substitution of Cl with EDA. The strength of the adsorption, as measured with the distribution coefficient, was greater for the former adsorbent than the latter. The origin of this difference was attributed to the distance between amino group and the surface. 相似文献
36.
We proposed and developed an exfoliation process for layer-structured NaxCoO2 to prepare CoO nanosheets. Na+ ion exchange by acid treatment was utilized to expand the spacing between the two CoO2 layers in NaxCoO2. Ethylamine was then effectively utilized for the exfoliation of cobalt oxide sheets having nanometer-order thickness and high aspect ratio. CoO nanosheets were observed by TEM micrographs and electron diffraction patterns after drying. Further efforts are needed for the application of exfoliated sheets to an integration process to fabricate self-assembled nanomaterials such as desired layer structures composed of two (or more) kinds of nanosheets. 相似文献
37.
Yoshitake Masuda Noriko Saito Rudolf Hoffmann Mark De Guire Kunihito Koumoto 《Science and Technology of Advanced Materials》2013,14(5):461-467
We proposed a novel method to fabricate nano/micro-scaled patterns of thin films and successfully fabricated patterns of anatase TiO2 thin films in an aqueous solution at 50 8C. The patterned self-assembled monolayer (SAM) having octadecyltrichlorosilane (OTS) regions and silanol regions was immersed in a solution containing a Ti precursor and subjected to ultrasonication for several hours. The difference in adhesion of thin films on substrates was employed for the site-selective elimination method. Heterogeneously nucleated TiO2 and homogeneously nucleated TiO2 particles adhering to the OTS–SAM could be easily eliminated from the substrate by ultrasonication, whereas those on silanol groups maintained their adhesion during the immersion period. TiO2 can form chemical bonds such as Ti–O–Si with silanol groups, but cannot form them with octadecyl groups, resulting in the difference in adhesion, which is the essence of the site-selectivity of this method. The site-selective elimination method can be applied to fabricate nano/micro-scaled patterns in the solution by the immersion of the substrate that has regions on which depositions adhere strongly and regions on which depositions adhere weakly, enabling elimination by treatment such as ultrasonication. © 2003 Elsevier Ltd. All rights reserved. 相似文献
38.
Hu X Masuda Y Ohji T Saito N Kato K 《Journal of nanoscience and nanotechnology》2011,11(12):10935-10939
Bunch-shaped ZnO nanowires film was successfully fabricated by the forced-hydrolysis-initiated-nucleation of anhydrous zinc acetate in an aqueous solution of zinc acetate and sodium hydroxide at low temperature. X-ray diffraction and a field emission scanning electron microscope clarified their formation mechanism and morphology development. The morphology was controllable by adjusting the solution temperature and deposition time. ZnO nanowires obtained at 65 degrees C for 6 h have a high aspect ratio of about 106. The smaller diameter with higher aspect ratio of ZnO nanowires, the easier the formation of bunch shapes by the capillary force during the drying process. This fabrication technique indicated that bunched ZnO film was prepared at low cost, and fittable to low heat-resistance substrates such as a polymer substarte. 相似文献
39.
Susumu Kashihara Shoji Otani Hironori Orikasa Yasuto Hoshikawa Jun-ichi Ozaki Takashi Kyotani 《Carbon》2012,50(9):3310-3314
A technique to determine a trace amount of hydrogen in carbon materials heat-treated above 1000 °C was developed. Three types of carbons prepared from poly(furfulyl alcohol), poly(vinyl chloride) and mesophase carbon microbeads were heat-treated at various temperatures ranging from 1000 to 1800 °C. Then they were gasified by O2 in a fixed bed flow reactor, and the H2O gases formed during the gasification processes were carefully monitored with a Karl Fischer moisture analyzer. As a result, this method makes it possible to determine the hydrogen contents in the carbons down to three places of decimals as a weight percent and can detect even a trace amount of hydrogen as low as 0.002 wt.%. A possible chemical structure of carbon edge sites was also discussed based on the experimentally determined hydrogen contents. 相似文献
40.
T. R. Allen J. I. Cole E. A. Kenik H. Tsai S. Ukai S. Mizuta T. Yoshitake 《JOM Journal of the Minerals, Metals and Materials Society》1999,51(10):27-30
An understanding of the effects of long-term, low-dose-rate radiation on core components is critical to light-water reactor
plant life extension. Following reactor shutdown, materials that had experienced long exposures to low-dose-rate irradiation
were retrieved from the EBR-II research reactor for analysis. These components are being analyzed to provide insight into
pressurized water reactor life extension. In this work, three examples of EBR-II materials analyses are highlighted: radiation-induced
segregation in 304 stainless steel, stress relaxation in Inconel X750, and swelling in 316 stainless steel.
For more information, contact T.R. Allen, Argonne National Laboratory-West, P.O. Box 2528, Idaho Falls, Idaho 83403-2528;(208)533-7760;
fax (208) 533-7863; e-mail todd.allen@anlw.anl.gov. 相似文献