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71.
    
To facilitate the dispersion of single‐walled carbon nanotubes (SWCNT) into poly(methyl methacrylate) (PMMA), SWCNT were functionalized with a RAFT chain transfer agent, and PMMA was grafted from the SWCNT by reversible addition–fragmentation transfer (RAFT) polymerization to give SWCNT‐g‐PMMA containing 6 wt % PMMA. SWCNT‐g‐PMMA in the form of small bundles was dispersed into PMMA matrices. The SWCNT‐g‐PMMA filler increased the glass transition temperature (Tg) of the composite when the matrix molecular weight Mn was less than the graft molecular weight, but not when the matrix Mn was equal to or greater than the graft Mn. The threshold of electrical conductivity of the composites as a function of weight percent SWCNT increased from 0.2% when matrix Mn was less than graft Mn to about 1% when matrix Mn was greater than graft Mn. Dynamic mechanical analyses of the composites having graft Mn less than or equal to matrix Mn showed broader rubbery plateaus with increased SWCNT content but no significant differences between samples with different grafted PMMAs. The results indicate that lower Mn matrix wets the SWCNT‐g‐PMMA whereas higher Mn matrix does not wet the SWCNT‐g‐PMMA. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39884.  相似文献   
72.
    
Shrinkage studies were conducted on silane‐grafted moisture crosslinkable linear low‐density polyethylene (LLDPE) insulation stripped from extrusion‐coated copper conductors. The insulation, which possesses orientation imparted during melt processing, showed remarkable levels of shrinkage when heated above the melting point of the polymer, though the shrinkage can be greatly reduced by moisture crosslinking the insulation below the melting point of the LLDPE. Shrinkage along the direction of orientation was accompanied by swelling in the other dimensions. Differential scanning calorimetry (DSC) revealed several trends, including a decrease in both melting point and degree of crystallinity with increasing crosslinking. In the first heat after annealing, crosslinked samples exhibited a shoulder in the DSC endotherm several degrees below the normal melting point of the LLDPE. In agreement with prior studies in silane‐grafted HDPE, relaxation of orientation by annealing appeared to result in an increase in the enthalpy of melting. The degree of shrinkage was also found to be dependent on the insulation thickness, which is attributed to faster cooling in thinner insulation immediately following extrusion coating. The results highlight the extensive built in stresses that can be frozen into polymer layers in fabricated articles due to melt orientation. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010  相似文献   
73.
    
In the present work, the metallocene‐based polyethylene–octene elastomer (POE) was chemically modified by solution grafting of acrylic acid in presence of benzoyl peroxide. The relative proportions of graft and gel formation were optimized through %weight gain, Fourier Transform infrared spectroscopy, elemental analysis and proton nuclear magnetic resonance spectroscopy. The gel formation in the POE matrix was found to be the prime competitor. The effect of grafting at its maximum level on various physicomechanical properties was thoroughly investigated, using X‐ray diffraction analysis, differential scanning calorimetry, mechanical, dynamic mechanical, and thermogravimetric analysis. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007  相似文献   
74.
    
In the present work, thermoplastic elastomer (TPE)–clay nanocomposites (TPN) based on different rubber–plastic blends from ethylene–octene copolymer [Engage]–Polypropylene and brominated poly(isobutylene‐co‐paramethyl styrene)–nylon 6 were prepared by melt blending. Hexadecyltrimethylammonium bromide and octadecyl amine‐modified sodium montmorillonite were used as organoclays. The nanocomposites were prepared by adding the nanoclay separately into the rubber and plastic phases. The TPNs were characterized with the help of transmission electron microscopy (TEM) and X‐ray diffraction. The X‐ray diffraction peaks observed in the range of 3–10° for the modified clays disappeared in the thermoplastic elastomeric nanocomposites. TEM photographs showed exfoliation and intercalation of the clays in the range of 20–30 nm in the particular phase where the clay was added. Excellent improvement in mechanical properties like tensile strength, elongation at break, and modulus was observed on incorporation of the nanoclays in the rubber phase of TPN. When the nanoclay was added to the plastic phase, the mechanical reinforcement is comparatively poorer due to partial destruction of the crystallinity. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1645–1656, 2006  相似文献   
75.
    
Single‐walled carbon nanotubes (SWCNTs) dispersed in N‐methylpyrrolidone (NMP) were functionalized by addition of polystyryl radicals from 2,2,6,6‐tetramethyl‐1‐piperidinyloxy‐ended polystyrene (SWCNT‐g‐PS). The amount of polystyrene grafted to the nanotubes was in the range 20‐25 wt% irrespective of polystyrene number‐average molecular weight ranging from 2270 to 49 500 g mol?1. In Raman spectra the ratios of D‐band to G‐band intensity were similar for all of the polystyrene‐grafted samples and for the starting SWCNTs. Numerous near‐infrared electronic transitions of the SWCNTs were retained after polymer grafting. Transmission electron microscopy images showed bundles of SWCNT‐g‐PS of various diameters with some of the polystyrene clumped on the bundle surfaces. Composites of SWCNT‐g‐PS in a commercial‐grade polystyrene were prepared by precipitation of mixtures of the components from NMP into water, i.e. the coagulation method of preparation. Electrical conductivities of the composites were about 10?15 S cm?1 and showed no percolation threshold with increasing SWCNT content. The glass transition temperature (Tg) of the composites increased at low filler loadings and remained constant with further nanotube addition irrespective of the length and number of grafted polystyrene chains. The change of heat capacity (ΔCp) at Tg decreased with increasing amount of SWCNT‐g‐PS of 2850 g mol?1, but ΔCp changed very little with the amount of SWCNT‐g‐PS of higher molecular weight. The expected monotonic decrease in ΔCp coupled with the plateau behavior of Tg suggests there is a limit to the amount that Tg of the matrix polymer can increase with increasing amount of nanotube filler. Copyright © 2012 Society of Chemical Industry  相似文献   
76.
77.
The plasma membrane Ca-ATPases play an important role in the regulation of intracellular Ca2+ ion concentration by pumping Ca2+ out of the cell into the extracellular fluid at the expense of ATP. These pumps potentially play an important role in the delivery of Ca2+ during mineralization of hard tissues such as bone. The properties of the plasma membrane Ca2+ pump are compared with those of the sarco(endo)plasmic reticulum and the factors regulating pump function are presented. The different gene products for the plasma membrane Ca-ATPases are described as well as their known functional significance. Particular attention is paid on the plasma membrane Ca2+ pumps present in mineralizing tissues and evidence supporting a role for these pumps in the transcellular delivery of Ca2+ during the process of mineralization is also presented.  相似文献   
78.
Saha  Abhijit  Mondal  Subhas Chandra 《SILICON》2019,11(3):1313-1326
Silicon - Wire electric discharge machining (WEDM) is a nontraditional machining technique to cut hard and conductive material with the assistance of a moving electrode. Nanostructured hardfacing...  相似文献   
79.
Present work describes a kinetic analysis of various aspects of biohydrogen production in batch test using optimized conditions obtained previously. Monod model and Logistic equation have been used to find growth kinetic parameters in batch test under uncontrolled pH. The values of μm, Ks, and Xm were 0.64 h−1, 15.89 g-COD L−1, and 7.26 g-VSS L−1, respectively. Modified Leudeking-Piret and Michaelis–Menten equation corroborates a flux of energy to hydrogen production pathway and energy sufficiency in the system. Modified Gompertz equation illustrates that the overall rate and hydrogen yield at 15 g-COD L−1 was higher compared to a dark fermentation of other wastewaters. Besides, Andrew's equation also suggests that since the higher value of KI (19.95 g-COD L−1), k (255 mL h−1 L−1) was not inhibited at high S. The experimental results implied that the entire products during the fermentation process were growth and substrate degradation associated. The result also confirms that the acetate and butyrate were substantially used for hydrogen production in acidogenic metabolism under uncontrolled pH.  相似文献   
80.
Ionic polymers, their blends and composites are considered potential candidates for application as electrolytes in fuel cells. While developing new materials for membranes, it is important to understand the interactions of these electrolytic materials with electrodes/catalysts and with reactants/products. Some of these interactions can be understood by estimating the surface energy and wettability of the membrane materials. In this work, polyvinyl alcohol with varying degrees of sulfonation and its blend with sulfonated poly(ether ether ketone) are prepared and studied for their wettability characteristics using goniometry. The surface energy and its components are estimated using different approaches and compared. Properties such as the ion-exchange capacity, the proton conductivity and the water sorption/desorption behaviour are also investigated to understand the relationship with wettability and surface energy and its components. Among the different methods, the van Oss acid-base and the modified Berthelot approaches yield comparable estimates for the total surface energy.  相似文献   
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