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991.
M. Hossein Nouri-Sorkhabi Lesley C. Wright David R. Sullivan Philip W. Kuchel 《Lipids》1996,31(7):765-770
31P Nuclear magnetic resonance (NMR) spectra of human erythrocyte lysates dissolved in sodium cholate were acquired. The narrow
resonances of phospholipids were mostly well resolved, allowing identification and accurate quantitative analysis of phospholipid
classes of the erythrocyte membranes. The ether-linked phosphatidylethanolamine components of the erythrocyte membranes were
identified, based on the removal of plasmalogens by acidolysis and of diacyl phospholipid species by degradation using phospholipase
A1. It was also shown that the introduction of double bonds on the acyl chains of phosphatidylcholine shifted the31P NMR resonances to lower frequencies. Quantitative analyses of phospholipids from the spectra were based on their apparent
molar concentrations. The recoveries of phospholipids from erythrocytes were significantly higher than those using conventional
extraction procedures. 相似文献
992.
The intact preen wax esters of the red knot Calidris canutus were studied with gas chromatography/mass spectrometry (GC/MS) and GC/MS/MS. In this latter technique, transitions from the
molecular ion to fragment ions representing the fatty acid moiety of the wax esters were measured, providing additional resolution
to the analysis of wax esters. The C21−C32 wax esters are composed of complex mixtures of hundreds of individual isomers. The odd carbon-numbered wax esters are predominantly
composed of even carbon-numbered n-alcohols (C14, C16, and C18) esterified predominantly with odd carbon-numbered 2-methyl fatty acids (C7, C9, C11, and C13), resulting in relatively simple distributions. The even carbon-numbered wax esters show a far more complex distribution
due to a number of factors: (i) Their n-alcohol moieties are not dominated by even carbon-numbered n-alcohol moieties are not dominated by even carbon-numbered n-alcohols esterified with odd carbon-numbered 2-methyl fatty acids, but odd and even carbon-numbered n-alcohols participate in approximately equal amounts; (ii) odd carbon-numbered methyl-branched alcohols participate abundantly
in these wax ester clusters; and (iii) with increasing molecular weight, various isomers of the 2,6-, 2,8-, and 2,10-dimethyl
branched fatty acids also participate in the even carbon-numbered wax esters. The data demonstrate that there is a clear biosynthetic
control on the wax ester composition although the reasons for the complex chemistry of the waxes are not yet understood. 相似文献
993.
Zdena Tvarůžková Magda Tupá Pavel Jírů Alfonso Nastro Giorgio Giordano Ferruccio Trifiró 《Catalysis Letters》1989,2(6):369-374
The small pore zeolite HLZ 132 exhibits, in comparison with other zeolites, an increased selectivity for the transformation of methanol to ethylene in the reaction temperature range 350–500 °C: the weight ratio of C2H4 to C3H6 in the products ranges between 1 and 4 at WHSV=2 h–1. Besides the effect of the reactant shape selectivity this fact may be interpreted by the participation of the asymmetrical methoxy groups in the surface as well as by proton-donor centres of lower acidity which do not catalyze the oligomerization of ethylene but which do the more basic molecule of propylene, thereby generating polyene-type coke. 相似文献
994.
Changes in south-east anatolian bitumens and their main fractions under various oxidative conditions
C. Tüzün F. Yaiz 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1973,23(11):781-802
Fractional analyses of South-East Anatolian bitumens were made using Marcusson's method and changes in fractional compositions and in functional groups under oxidative conditions were investigated. A more detailed study was carried out on the asphaltic resins fraction of bitumen of Ma?rip origin, since, of those tested, this bitumen proved to be the most susceptible to oxidative conditions. 相似文献
995.
Catalysts based in cerium oxide for wet oxidation of acrylic acid in the prevention of environmental risks 总被引:3,自引:0,他引:3
Adrin M. T. Silva Rita R. N. Marques Rosa M. Quinta-Ferreira 《Applied catalysis. B, Environmental》2004,47(4):269-279
Acrylic acid is a refractory compound for the non-catalytic wet oxidation (WO) process and can seriously damage the environment when released in industrial effluents. Oxidation of acrylic acid by catalytic wet oxidation (CWO) was studied in slurry conditions in a high-pressure batch reactor at 200 °C and 15 bar of oxygen partial pressure. Several solid cerium-based catalysts prepared in our laboratory were used (Ag/Ce, Co/Ce, Mn/Ce, CeO, MnO) and evaluated in terms of activity, selectivity and stability. Mn/Ce shows the higher activity in 2 h with 97.7% reduction of total organic carbon (TOC) followed by: MnO(95.5%)>Ag/Ce(85.0%)>Co/Ce(65.1%)>CeO(61.2%). Attempts were also carried out to analyze the influence of different Mn/Ce molar ratios. High percentages of Mn lead to practically total organic carbon concentration (TOC) abatements while low ratios lead to the formation of non-oxidizable compounds. Acrylic acid was readily degraded by all the catalysts pointing out the high importance of using a catalytic process. pH was an indicator of the reaction pathway and acetic acid was found as the major reaction intermediate compound; however it is completely oxidized after 2 h with exception for Co/Ce, CeO and MnO. Carbon adsorption and leaching of metals were poorly found for Mn/Ce indicating high stability. The catalyst microstructure after the reaction was analyzed and formation of whiskers of β-MnO2 (or less probably MnOOH) were observed at the catalyst surface. Therefore, Mn/Ce revealed to be a promising catalyst for the treatment of effluents containing acrylic acid; nevertheless, its commercialization depends on further research. 相似文献
996.
Filiberto González Garcia Bluma G. Soares Victor J. R. R. Pita Rubén Sánchez Jacques Rieumont 《应用聚合物科学杂志》2007,106(3):2047-2055
The mechanical properties of epoxy networks based on diglycidyl ether of bisphenol A epoxy resin cured with various linear aliphatic amines, such as ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, and cyclic amines such as 1‐(2‐aminoethyl)piperazine and isophorone diamine, were studied. General characteristics such as Tg, density, and packing density, were determined and related to the structure and funcionality of the curing agent. Dynamic mechanical spectra were used to study both the α and β relaxations. Tensile and the flexural tests were used to determine the Young's and flexural modulus, and fracture strength all in the glassy state. Furthermore, linear elastic fracture mechanics was used to determine KIC. As a rule, isophorone diamine network presented the higher tensile and flexure modulus while 1‐(2‐aminoethyl)piperazine gave the highest toughness properties. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 相似文献
997.
网络化雷达在战场上可以构成全方位、立体化、多层次的战斗体系,因
此对欺骗式干扰对抗具有很大的优越性。本文首先简要介绍了网络化雷达概念,并分析了其
抗干扰优势。根据网络化雷达融合结构不同,将现有协同抗干扰方法分为数据级融合抗欺骗
式干扰和信号级融合抗欺骗式干扰两大类,其中,数据级融合方法进一步分类为点迹关联和
航迹关联两类。本文对各类方法进行了详细介绍,在此基础上,比较分析了数据级融合和信
号级融合两类方法的抗干扰性能及算法复杂度,为抗干扰措施的选择提供依据。最后,针对
现有方法中存在的问题,对网络化雷达协同抗欺骗式干扰的发展趋势进行展望,指出下一步
的研究方向。 相似文献
998.
Z. Benzo T. Zoltan M. Murillo M. Quintal J. Salas E. Marcano C. Gómez 《Journal of the American Oil Chemists' Society》2006,83(5):401-405
An emulsion-based method was developed as an alternative for the introduction of oil-based samples into a graphite furnace
to produce a more rapid, precise, and accurate method of analysis. The combination of emulsion sampling and electrothermal
atomization for atomic absorption spectroscopy was developed and then applied to the determination of Ni and manganese in
neem oil from Venezuela. The optimal concentration of neem oil in the emulsion was 30 and 4% for Ni and Mn, respectively,
based on the metal concentration of the neem oil. The stability of the emulsion as a function of time was evaluated. The use
of aqueous calibration solutions and the accuracy attained using this method make it attractive for the analysis of oil samples.
The metal recovery was between 97 and 101%. Based on the emulsion method, the neem oil samples had 1.39 and 0.21 mg of Mn
and Ni per kg of oil, respectively. The wet digestion method indicated a Mn and Ni concentration in the neem oil sample of
1.42 and 0.24 mg/kg, respectively. 相似文献
999.
F.J. Medellín‐Rodríguez J.M. Mata‐Padilla B.S. Hsiao M.A. Waldo‐Mendoza E. Ramírez‐Vargas S. Sánchez‐Valdes 《Polymer Engineering and Science》2007,47(11):1889-1897
The influence of organomodified nanoclay (montmorillonite) on the crystallization and melting mechanisms of isotactic polypropylene (iPP) was studied. Films of both neat polymer and clay nanocomposites were prepared after molecular weight optimization through melt extrusion. Products exhibited the tactoidlike morphology since no compatibilizers were used. The effect of introduction of nanoclay within the polymer was studied through isothermal crystallization and linear heating. The results indicated that low nanoclay concentrations induce the formation of the β‐crystalline structure, its formation being inhibited with high nanoclay contents. Dynamic nonisothermal bulk crystallization experiments indicated that nanoclays act as nucleating agents of iPP. Isothermal, bulk crystallization studies indicated that the crystallization process (induction time and crystallization kinetics) is proportionally accelerated by the nanoclay presence. There was also an accelerated formation of secondary crystallization when nanoclays were present in high concentrations. POLYM. ENG. SCI., 47:1889–1897, 2007. © 2007 Society of Plastics Engineers 相似文献
1000.
A. Serrano Aroca A.J. Campillo Fernndez J.L. Gmez Ribelles M. Monlen Pradas G. Gallego Ferrer P. Pissis 《Polymer》2004,45(26):8949-8955
Dynamic-mechanical and water sorption properties of porous and non-porous hydrogels have been studied as a function of their porosity and crosslinking density. Porous hydrogels with different crosslinking densities were prepared by co-polymerisation of 2-hydroxyethyl acrylate and ethyleneglycol dimethacrylate in solution in methanol. Pores were formed due to the segregation of the solvent from the polymer network during the polymerisation process. The porosity of the samples was observed by scanning electron microscopy. The pores collapse during the drying process after polymerisation but they reopen when the xerogel is immersed in liquid water. Bulk polymer networks with varying crosslinking densities were also synthesised and used as a reference in the analysis of the porous hydrogels. Water sorption from the gas phase and from the liquid phase was studied by means of equilibrium sorption isotherms and immersion experiments, respectively. Dynamic-mechanical spectroscopy conducted on the xerogels shows that the elastic modulus in the rubber-like state highly depends on the amount of solvent used in the polymerisation what is attributed to the presence of discontinuity surfaces in the xerogel although the pores are closed. 相似文献