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51.
A series of new alkene and octenyloxy monomers containing 4′-[oligo(ethylene oxide)] n monomethyl ether 4-biphenyl ether carboxyl benzoate [MS3BDBEn] (n = to 3) and 1- (p-methoxydiphenyl)–(carboxyl benzoate) [oligo(ethylene oxide)]n [MSm+2BEnDB] (m = 1, 6; n = 1 to 3) as end groups were synthesized. The molecular structure of the monomers was charaterized using nuclear magnetic resonance (NMR) spectroscopy. These monomers were grafted onto poly(methylhydrosiloxane)s (PMHS) by the platinun-catalyzed hydrosilylation process. The thermal transition temeratures and mesophase textures of the monomers and the polysiloxane polymers have been determined by diffential scanning calorimetry (DSC) and by polarized optical microscopy. The effect of changes in chemical structure on the mesophase properties, glass transition temperature, isotropic temperature, and mesophase texture of the monomers and the polysiloxane polymers is discussed. Polymers PS3BDBEn showed smectic and nematic phases which were not analogous to their precursor nematic monomers MS3BDBEn. Both monomers MSm+2BEnDB and their polymeric homologous PSm+2BEnDB did not exhibit mesophase properties. This demonstrated that the polymer effect could not stabilize the mesophase obtained from mesogenic core which contained a flexible oligo(ethylene oxide) unit interconnecting aromatic group. © 1995 John Wiley & Sons, Inc. 相似文献
52.
This paper examines the linear elastic tensile and fracture behavior of biaxial plain weave SiC/SiC ceramic woven fabric composites. Iso-phase mode and random-phase mode have been adopted to simulate multilayer stacking and to predict the initial linear elastic constants. It has been found that both modes predict very close results. Porosities in the composite affect the stiffness significantly, while fiber undulation shows only minimal effect. The nonlinear stress-strain relation of the composite is due to transverse cracks, which initiate mainly from interyarn pores. In the second part of this paper, two methods, classical fracture mechanics and energy balance approach, have been used to examine the crack initiation and growth. A finite element method and a modified shear-lag method have been developed to evaluate the stress distribution in the yarn with transverse cracks. The composite stiffness reduction due to transverse cracking has been obtained by both the finite element and shear-lag methods. Strain energy release rates of the growth of transverse cracks have been studied by the crack-closure procedure, using finite element methods. Effects of the yarn size and crack position on the strain energy release rate have been quantified. It is concluded that thinner yarns lead to higher critical strains for transverse cracking. 相似文献
53.
Poly(vinyl pyrrolidone‐co‐isobutyl styryl polyhedral oligomeric silsesquioxane)s (PVP–POSS) were synthesized by one‐step polymerization and characterized using FTIR, high‐resolution 1H‐NMR, solid‐state 13C‐NMR, 29Si‐NMR, GPC, and DSC. The POSS content can be controlled by varying the POSS feed ratio. The Tg of the PVP–POSS hybrid is influenced by three main factors: (1) a diluent role of the POSS in reducing the self‐association of the PVP; (2) a strong interaction between the POSS siloxane and the PVP carbonyl, and (3) physical aggregation of nanosized POSS. At a relatively low POSS content, the role as diluent dominates, resulting in a decrease in Tg. At a relatively high POSS content, the last two factors dominate and result in Tg increase of the PVP–POSS hybrid. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2208–2215, 2004 相似文献
54.
Jui‐Ming Yeh Chi‐Lun Chen Tai‐Hung Kuo Wen‐Fen Su Hsi‐Ya Huang Der‐Jang Liaw Hsin‐Yi Lu Chi‐Fong Liu Yuan‐Hsiang Yu 《应用聚合物科学杂志》2004,92(2):1072-1079
A series of polymer–clay nanocomposite (PCN) materials consisting of 1,4‐bis(4‐aminophenoxy)‐2‐tert‐butylbenzene–4,4′‐oxydiphthalic anhydride (BATB–ODPA) polyimide (PI) and layered montmorillonite (MMT) clay were successfully prepared by an in situ polymerization reaction through thermal imidization up to 300°C. The synthesized PCN materials were subsequently characterized by Fourier‐Transform infrared (FTIR) spectroscopy, wide‐angle powder X‐ray diffraction (XRD) and transmission electron microscopy (TEM). The effects of material composition on thermal stability, mechanical strength, molecular permeability and optical clarity of bulk PI and PCN materials in the form of membranes were studied by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), molecular permeability analysis (GPA) and ultraviolet‐visible (UV/VIS) transmission spectra, respectively. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1072–1079, 2004 相似文献
55.
Optically active 2-endo-actoxy-5-endo-bornyl methacrylate (ABMA) was prepared from (+)-camphor. The homopolymerization of ABMA and copolymerization of ABMA with achiral methyl methacrylate (MMA) or styrene (St) were carried out with 2,2′-azobisisobutyronitrile (AIBN) in benzene. Effects of temperature, solvents, and reaction time on the copolymerization were discussed. The monomer reactivity ratios(r1, r2) for poly(ABMA-co-MMA) and poly(ABMA-co-St) and Q and e values for the chiral ABMA in the copolymerization systems were evaluated by the Fineman—Ross method. The absolute value of the specific rotation of poly(ABMA-co-MMA) increased with increasing ABMA unit content. A small deviation from linearity was observed, which suggests that asymmetry is not introduced into the copolymer main chain. Temperature and solvent effects on the specific rotation of the chiral homopolymer and copolymers were investigated. The results suggest that the chiral polymers synthesized in this investigation did not show a strong preference for a particular helical conformation. Applications of the chiral polymers on the asymmetric addition of n-butyllithium to aldehydes were also discussed. 相似文献
56.
Carbon/carbon composites were made through the pyrolysis of stabilized PAN felt and phenolic resin with the addition of 5 or 10 wt % carbon black to the matrix and then heat treatment at 600–2500°C. The effects of adding carbon black to the matrix precursor on the physical properties, microstructure, and mechanical properties of the resultant composites were investigated. Adding carbon black not only reduced the weight loss but also limited the shrinkage of the resultant composites. Adding carbon black also accelerated the formation of carbon basal planes in the matrix. At 2500°C, the crystalline stacking height in the composite with 10 wt % added carbon black was 200% greater than that with no additive. The flexural strength of the composite also increased from 15 to 42 MPa (almost 300%). © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 333–337, 2006 相似文献
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<正>作者等过去的工作已经证实,由于扩散过程的影响、温度范围的不同、或化学组成的差异,二氧化硫在钒催化剂上的氧化动力学方程式可能具有不同的形式。反应物及生成物与催化剂之间的相互作用,可能使催化剂具有不同的颜色与活性,因而即使温度相同,由于催化剂在层内所处的部位不同,其催化活性可能并不一致。这些复杂性给工业设计带来了很大的困难。因此,合理的简化是完全必要的。 作者等选取了几种不同的工业钒催化剂,用实验方法求得了适用于它们的动力学方程式,进行比较和讨论,提出了一个简便的、合理的、可以用作设计基础的动力学方程式。 相似文献
60.
This study investigates the growth mechanism of IC compatible processes and to the feasibility of synthesizing networks of single-walled carbon nanotubes (SWNTs) at lower temperatures (610 °C) on Si wafer using microwave plasma chemical vapor deposition (MPCVD) with CH4 and H2 as source gases. The effects of the buffer layer materials (ZnS–SiO2, Al2O3, AlON, and AlN ) and process conditions on growth of carbon nanostructures with Co as catalyst were also examined, where the buffer layers and Co catalyst were deposited in sequence by physical vapor deposition (PVD), followed by H-plasma pretreatment before deposition of carbon nanostructures. Additionally, the morphologies and bonding structures of carbon nanostructures were characterized by field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), and Raman Spectroscopy. Analytical results demonstrate that networks of SWNTs are more favorable to be synthesized by selecting proper buffer layer material (e.g., AlON), and under higher temperatures, thinner catalyst thickness (e.g., 5 nm) and lower CH4 / H2 ratio (e.g., 5 / 100 sccm/sccm). The networks of SWNTs can be fabricated at temperatures as low as 610 °C by manipulating these parameters. In conclusion, the growth mechanism determines the conditions for the formation of nano-sized extrusions on catalyst particles surface. 相似文献