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41.
S. Sakkopoulos E. Vitoratos E. Dalas N. Kyriakopoulos P. Malkaj T. Argyreas 《应用聚合物科学杂志》2005,97(1):117-122
The dc electrical conductivity (σ) of HCl‐protonated polyaniline, polypyrrole, and their blends was measured from 80 to 300 K for thermal aging times between approximately 0 and 600 h. The thermal aging took place at 70°C under room atmosphere. The change of σ with the temperature (T) and the decrease of σ with the thermal aging time (t) are consistent with a granular metal type structure, in which conductive grains are randomly distributed into an insulating matrix. Aging makes the grains shrink in a corrosion‐like process. From σ = σ(T) measurements the ratio s/d, where s is the average separation between the grains and d their diameter, as well as the rate d(s/d)/dt of their decrease with t were calculated. These revealed that the conductive grains consist of a shell, in which aging proceeds at a decreasing rate, and a central core, which is consumed at a much slower rate. Our measurements not only permitted the estimation of the shell thickness, which lies between 0 and 5 Å, but also gave quantitative information about the quality of the shells and the cores from their aging rates. The shells are consumed with an average rate of d(s/d)/dt = 6.6 × 10?4 (h?1), which is about 5 times greater than the more durable cores. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 117–122, 2005 相似文献
42.
本文研究了炭黑-环氧树脂复合材料的制备工艺及炭黑填充率对材料电阻率的影响。实验结果表明,加入表面活性剂,明显改善了炭黑在环氧树脂中分布的均匀性。炭黑-环氧树脂材料具有明显的渗流效应,正温度系数效应即PTC效应,非线性伏安特性和电磁波屏蔽效应。 相似文献
43.
用多元乳液共聚法制备了用于粘贴导静电PVC地板胶粘剂,加入乙炔碳黑赋予乳液胶粘剂导静电性能。研究了影响胶接强度和初粘力的主要因素,确定m(VAc)/m(BA+VAc)较合适比为1∶3;研究了乳化剂和交联单体对乳液性能的影响,研究得出,适量加入AA和HMAM可以减少乳化剂的用量,提高乳液的性能;考查了影响导静电性能的因素,研究表明,导静电性能由乙炔碳黑决定,其加入量越大,导静电性能越好。得到的导静电乳液胶粘剂胶接强度达到0.51MPa以上,导静电可达到7.2×103Ω,两项指标均超过国家标准。 相似文献
44.
Polypyrrole (PPY) and PPY/SBA‐15 host–guest composite materials have been prepared using chemical synthesis route and characterized by XRD, IR, N2 adsorption–desorption isotherms, and SEM. The humidity sensitive properties (HSP) of this kind of materials have been studied by analyzing the variation curve of impedance as a function of relative humidity. It was found that the PPY/SBA‐15 host–guest composites materials exhibit better HSP than that of the corresponding pure PPY. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3301–3305, 2006 相似文献
45.
46.
To overcome the problems relevant to the low processbility and scarce mechanical properties of polyaniline, in a previous work we have proposed the synthesis of elastomeric conducting copolymers prepared by grafting polyaniline (EB) or sulfonated polyaniline (SPAN) chains to the backbone of a carboxylated segmented polyurethane (PEUA). In the present work the physical and chemical‐physical properties of the copolymers are investigated. As evidenced by thermal (DSC) and dynamo‐mechanical (DMTA) characterization, the introduction of EB or SPAN in the matrix enhances the hard‐soft phase segregation effect, because of the strong tendency of the conductive polymer chains to aggregate. Moreover, the EB and SPAN chains, grafted to the polyurethane backbone, acting as reinforcing filler, give rise, compared with the mechanical properties of the insulating matrix, to an increase of the Young modulus and a decrease of the tensile set. When the copolymers are HCl doped their electrical conductivity increases many orders of magnitude, reaching values of about 10?3 Ω?1 cm?1. The conductivity, measured along the deformation direction, may be further increased by stretching the copolymer films. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1259–1264, 2002 相似文献
47.
The copolymerization of carbazole (CZ) and 3‐methylthiophene (3MeT) was successfully performed electrochemically in freshly distilled boron trifluoride diethyl etherate by direct anodic oxidation of the monomer mixtures, although the oxidation potentials of CZ and 3MeT were quite different. The electrochemical properties of the copolymers were studied with cyclic voltammetry. The influence of the applied polymerization potential on the synthesis of the copolymers was investigated. The higher potential favored the incorporation of 3MeT units into the copolymers. The insertion of 3MeT units into polycarbazole (PCZ) was helpful in improving the conductivity of PCZ. The novel copolymers had the advantages of both PCZ and poly(3‐methylthiophene), that is, good redox activity, good thermal stability, and high conductivity. The structure and morphology of the copolymers were investigated with ultraviolet–visible, infrared spectroscopy, thermal analysis, and scanning electron microscopy. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1877–1885, 2006 相似文献
48.
A novel method for the preparation of electrically conducting fibers through chemical grafting of electrically conducting polymer onto poly(propylene) (PP) fiber is described. The graft copolymerization of aniline (ANI) was performed in aqueous acidic medium by using a chemical oxidant such as peroxydisulfate (PDS). Grafting occurred with simultaneous homopolymer formation. The content of polyaniline in the backbone fiber was found to vary by varying [monomer], [initiator], and amount of PP fiber. Various graft parameters such as rate of grafting (Rg), % grafting, and % grafting efficiency were evaluated. The rate of homopolymerization (Rh) was also determined. Both Rh and Rg showed first‐order dependency on [ANI], [PDS], and amount of PP fiber variation. The chemical grafting was confirmed by use of cyclic voltammetry and conductivity measurements. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3827–3834, 2003 相似文献
49.
Poly(methylphenylene) (PMeP) films were prepared by direct oxidation of toluene in the mixed electrolytes of boron trifluoride diethyl etherate (BFEE) and trifluoroacetic acid (TFA). The oxidation potential of toluene in pure BFEE was measured to be 1.52 V versus saturated calomel electrode (SCE). This value was much lower than that determined in a neutral medium such as acetonitrile (2.13 V versus SCE). The introduction of TFA into BFEE decreased the oxidation potential of toluene and also improved the properties of as‐formed polymer films. Infrared and Raman spectra confirmed the formation of PMeP films. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 189–195, 2004 相似文献
50.
Rinaldo Gregorio Luiz Francisco Malmonge Guilherme Fontes Leal Ferreira Wilson Nunes Dos Santos Luiz Henrique Capparelli Mattoso 《应用聚合物科学杂志》2003,87(5):752-758
The real (ε′) and imaginary (ε″) components of the complex permittivity of blends of PVDF [poly(vinylidene fluoride)] with POMA [poly(o‐methoxyaniline)] doped with toluenosulfonic acid (TSA) containing 1, 2.5, and 5 wt % POMA–TSA were determined in the frequency interval between 102 and 3 × 106 Hz and in the temperature range from ?120 up to 120°C. It was observed that the values of ε′ and ε″ had a greater increase with the POMA–TSA content and with a temperature in the region of frequencies below 10 kHz. This effect decreased with frequency and it was attributed to interfacial polarization. This polarization was caused by the blend heterogeneity, formed by conductive POMA–TSA agglomerates dispersed in an insulating matrix of PVDF. The equation of Maxwell–Garnett, modified by Cohen, was used to evaluate the permittivity and conductivity behavior of POMA–TSA in the blends. A strong decrease was observed in POMA–TSA conductivity in the blend, which was bigger the lower the POMA–TSA content in the blend. This decrease could have been caused either by the POMA dedoping during the blend preparation process or by its dispersion into the insulating matrix. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 752–758, 2003 相似文献