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21.
A. Tabata  K. Fukaya 《Vacuum》2008,82(8):777-781
Hydrogenated microcrystalline silicon (μc-Si:H) thin films were prepared on glass, aluminum-covered glass and Si wafer substrates at various substrate bias voltages (Vsb) between -400 and +50 V, and the influence of Vsb on their structural properties was investigated. The crystallinity (crystalline volume fraction and crystallite size) of the μc-Si:H films deposited on glass remained unchanged with respect to Vsb. For μc-Si:H films deposited on aluminum within the Vsb range of -20 to +50 V, the crystallinity also remained unchanged and showed the same crystallinity as that of the films deposited on glass substrate. However, the crystallinity of the μc-Si:H films deposited on aluminum-covered substrate was reduced as Vsb decreased from -20 to -100 V, and the film at Vsb=-400 V was completely amorphous.  相似文献   
22.
Silk sericin (SS)/silk fibroin (SF) blend nanofibers have been produced by electrospinning in a binary SS/SF trifluoroacetic acid (TFA) solution system, which was prepared by mixing 20 wt.% SS TFA solution and 10 wt.% SF TFA solution to give different compositions. The diameters of the SS/SF nanofibers ranged from 33 to 837 nm, and they showed a round cross section. The surface of the SS/SF nanofibers was smooth, and the fibers possessed a bead-free structure. The average diameters of the SS/SF (75/25, 50/50, and 25/75) blend nanofibers were much thicker than that of SS and SF nanofibers. The SS/SF (100/0, 75/25, and 50/50) blend nanofibers were easily dissolved in water, while the SS/SF (25/75 and 0/100) blend nanofibers could not be completely dissolved in water. The SS/SF blend nanofibers could not be completely dissolved in methanol. The SS/SF blend nanofibers were characterized by Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry, and differential thermal analysis. FTIR showed that the SS/SF blend nanofibers possessed a random coil conformation and ß-sheet structure.  相似文献   
23.
The spent fuel characteristics of the reduced-moderation water reactor (RMWR) have been investigated using the SWAT and ORIGEN codes. RMWR is an advanced LWR concept for plutonium recycling by using the MOX fuel. In the code calculation, the ORIGEN libraries such as one-group cross-section data prepared for RMWR were necessary. Since there were no open libraries for RMWR, they were produced in this study by using the SWAT code. New libraries based on the heterogeneous core modeling in the axial direction and with the variable actinide cross-section (VXSEC) option were produced and selected as the representative ORIGEN libraries for RMWR. In order to investigate the characteristics of the RMWR spent fuel, the decay heat, the radioactivity and the content of each nuclide were evaluated with ORIGEN using these libraries. In this study, the spent fuel characteristics of other types of reactors, such as PWR, BWR, high burn-up PWR, full-MOX-PWR, full-MOX-BWR and FBR, were also evaluated with ORIGEN.

It has been found that about a half of the decay heat of the RMWR spent fuel comes from the actinides nuclides. It is the same with the radioactivity. The decay heat and the radioactivity of the RMWR spent fuel are lower than those of full-MOX-LWRs and FBR, and are the same level as those of the high burn-up PWR. The decay heat and the radioactivity from the fission products (FPs) in the spent fuel mainly depend on the burn-up and the burn-up time rather than the reactor type. Therefore, the decay heat and the radioactivity from FPs in the RMWR spent fuel are smaller, reflecting its relatively long burn-up time resulted from its core characteristics with the high conversion ratio. The radioactivity from the actinides in the spent fuel mainly depends on the 241Pu content in the initial fuel, and the decay heat mainly depends on 238Pu and 244Cm. The contribution of 244Cm is much smaller in RMWR than in MOX-LWRs because of the difference in the spectrum. In addition, from the waste disposal point of view, the characteristics of the heat generation FP elements, the platinum group metals, Mo and the long-lived FPs (LLFPs) were also investigated.  相似文献   

24.
A relation was obtained between electro-chemical properties of sodium salts (NaCl, NaBr, and Na2SO4), and the thermodynamic property of permeability in symmetrical cellulose acetate membranes, the distribution coefficient K and the kinetic property, the overall diffusion coefficients D. K and D were obtained by the method we proposed using measured unsteady- and steady-state dialysis data. The K values increase with the increase of water content and are in the range of 10−2 for sodium halides and 10−3 for Na2SO4. D is found to increase with the increase of the solute concentration, and the extrapolated values of D to zero concentration D(0) are obtained as 0.015–0.03 μm2/s and increase with the increase of water content in the membrane. D can be divided into the concentration independent diffusion coefficients in the dense part of the membrane Dd and in the porous Dp, applying a two-part (perfect or dense and imperfect or porous) model of the membrane. Contrary to Dd, Dp increases with the increase of Ww and can be correlated as Dp,c = d exp (γ × Ww). It is shown that the averaged Dd, D increases with the increase of the quantity of the ionic mobility u of the solutes at infinite dilution divided by valence, and that the parameter γ increases with the increase of the ionic mobility u. The value of K increases slightly with the increase of water content and decreases with the increase of the Flory—Huggins parameter χ. The Flory—Huggins parameter χ is calculated from the measured values of distribution coefficients and data obtained from the literature. And it was found that the gradient of linear decrease of χ (λcation) depends on equivalent ionic conductivity of anion of salt, λan.  相似文献   
25.
The graft–copolymerization of silk with methacrylamide (MAA), 2‐hydroxyethyl methacrylate (HEMA), and methyl methacrylate (MMA) was studied using three different free‐radical initiators: an inorganic peroxide [ammonium persulfate (APS)] and two azo compounds [2,2′‐azobisisobutyronitrile (AIBN) and 2,2′‐azobis(2‐methylpropionamidine) dihydrochloride (ADC)]. The rate and yield of grafting followed the order: APS > AIBN > ADC. The performance of AIBN was close to that of APS in terms of weight gain attained. The degree of yellowing of grafted silk varied as a function of the initiator–monomer system used. APS induced the highest degree of yellowing, regardless of which monomer was used, whereas silk grafted with the MAA/AIBN system displayed the lowest level of yellowing. Moisture regain of grafted silk changed as a function of the hydrophilic/hydrophobic character of the grafted polymer, regardless of the kind of initiator used. Accordingly, tensile properties showed a tendency to decrease with increasing weight gain of grafted silk, the extent of which was independent of the kind of monomer and initiator used. The different initiators did not induce any appreciable change in the fine structure of silk, as demonstrated by optical measurements. Uneven surface deposition of homopolymer was detected to variable extent with MMA and HEMA grafting, whereas the surface of MAA‐grafted silk was completely free of any foreign deposit, independently of the initiator used. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 1401–1409, 2001  相似文献   
26.
The method of implicit curve-fitting and explicit-calculation has been used for fast and stable calculations of thermodynamic properties of subcritical refrigerants. In order to extend that method to the critical pressure, a method of sectional implicit curve-fitting and explicit-calculation for refrigerant thermodynamic properties is introduced in this paper. The whole data range is divided into several subsections. The requirements on the continuity of thermodynamic properties and the first order derivative of thermodynamic properties in the intersection points of subsections are indicated, and the methods to meet the requirements are presented. Quadric equations are constructed instead of curve-fitting when no data can be given. With the source data obtained from REFPROP 7.1, explicit fast calculation formulae for thermodynamic properties of R410A, covering the saturated temperature of 213.15–344.51 K and superheat of 0–65 K, are given as an example. The calculation speeds of the formulae of R410A are more than 7000 times faster than those of REFPROP 7.1 while the total mean relative deviation of the fast calculation formulae from REFPROP 7.1 is only 0.04%.  相似文献   
27.
28.
Immunolocalization of transforming growth factor-alpha (TGF alpha), epidermal growth factor (EGF), cripto-1, amphiregulin and epidermal growth factor receptor (EGFR) was studied in 51 premenopausal human ovaries at various phases of the menstrual cycle. Localization of mRNA for TGF alpha and EGF was also studied by in-situ hybridization. Immunoreactive TGF alpha was observed predominantly in theca cells in 12 of 33 antral follicles in the follicular phase (6/14 dominant follicles, and 6/19 non-dominant) but not in any of the 18 follicles in the luteal phase or in primordial and pre-antral follicles. TGF alpha immunoreactivity was present predominantly in the luteinized granulosa cells in 13 of 15 corpora lutea in the luteal phase, which are considered to be active in steroidogenesis, but not in any of the regressed corpora lutea. Accumulation of TGF alpha mRNA hybridization signal was observed only in the theca cells in the follicles and luteinized theca cells in the ovaries that were immunohistochemically positive for TGF alpha. EGFR immunoreactivity was detected in 24 of 33 antral follicles in the follicular phase and in two of 18 follicles in the luteal phase but not in any of the corpora lutea. Immunoreactive EGF, cripto-1 and amphiregulin or EGF mRNA was not detected in any follicles, corpora lutea, or the stroma cells examined. These results indicate that, of the epidermal growth factors examined in this study, TGF alpha is locally synthesized in normal cycling human ovaries and TGF alpha may be synthesized in theca cells and act on the granulosa cells in a paracrine fashion through the EGFR in ovarian follicles.  相似文献   
29.
This paper deals with the physical properties of silk fibers grafted with 2-hydroxyethyl methacrylate (HEMA). Both tensile strength and elongation measured in the dry and wet states gradually decreased with increasing weight gain. The initial modulus of the grafted silk fibers in the dry state sharply increased in the weight gain range of 0–16%, then decreased to a lower value than the reference untreated sample. The refractive indices parallel and perpendicular to the fiber axis decreased, though the former showed a steeper slope. Accordingly, birefringence and isotropic refractive index also decreased, suggesting a lower degree of crystallinity and molecular orientation of grafted silk fibers. DSC, TMA, and TGA curves of the HEMA-grafted silk fibers indicated an increased higher thermal stability of silk fibers due to the HEMA grafting. The dynamic mechanical measurements showed that the thermally induced molecular movement of both amorphous and crystalline domains of silk fibers was enhanced by HEMA grafting. X-ray diffraction curves, however, implied that the crystalline structure of the silk fibroin remained unchanged regardless of HEMA polymerization. The introduction of HEMA polymer in silk fibers was evidenced by the infrared spectra, exhibiting the absorption bands characteristic of either the grafted HEMA polymer and the fibroin molecules with ordered β structure. © 1993 John Wiley & Sons, Inc.  相似文献   
30.
The structural characteristics, physical properties, and dyeing behavior of Bombyx mori silk fibers containing ethoxyethylmethacrylate (ETMA) polymer are reported in relation to the add-on. The add-on value increased with the reaction time and attained a maximum after 60 min at 80°C. The surface of silk fibers with an add-on value of 40% showed the presence of several irregular granules, consisting of ETMA oligomers. The infrared spectrum of the silk fibers containing the ETMA polymer showed overlapped absorption bands due to the molecular conformation of untreated silk and ETMA polymer, giving evidence that the ETMA polymerization occurred inside the fiber matrix. The DSC results suggested that the thermal decomposition behavior of the silk fiber remained almost unchanged, except that the decomposition temperature shifted slightly to higher temperature. The tensile properties of the silk fiber remained unchanged regardless of the ETMA polymerization. The rate and extent of acid dye uptake was greatly increased by the polymerization of ETMA into the silk fibers as well as the transfer printing properties.  相似文献   
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