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71.
72.
C. D. Evans G. R. List Helen A. Moser J. C. Cowan 《Journal of the American Oil Chemists' Society》1973,50(6):218-222
Commercially prepared and packaged soybean and cottonseed salad oils from several different processors were evaluated periodically
during storage for 12 months. Partially hydrogenated and winterized soybean oils, as well as unhydrogenated soybean salad
oils, were stored in bottles and cans at 78 and 100 F. Control samples of all oils were held at 0 F during the entire test.
Some lots in bottles and cans were packaged under nitrogen to improve storage stability. Agreement was good between organoleptic
and oxidative evaluation of aged oils. After 26 weeks of storage at 100 F, the flavor of partially hydrogenated-winterized
oils packaged under nitrogen showed a minimum loss. These same oils did not exhibit much, if any, reduction in their oxidative
stability as indicated by storage peroxide values (active oxygen method). Soybean oil not protected with nitrogen demonstrated
progressive flavor deterioration at 100 F. After 10 weeks of storage, the deterioration became marked and the flavor score
was below 5. From limited observations, bottled oils appear to have a better stability than oils packaged in screw-cap tin
cans. Hydrogenated oils packaged under nitrogen in cans had good oxidative stability, but some lowering of the flavor score
was observed. Nonhydrogenated soybean oils packaged in tin cans not under nitrogen exhibited the most rapid flavor deterioration
of all lots of oil investigated.
Presented in part at the AOCS meeting, New York, October 1968
ARS, USDA 相似文献
73.
A comprehensive experimental study concerning the influence of various types of initiator-emulsifier systems on emulsion polymerization of methacrylate monomers (2-hydroxyethyl methacrylate (HEMA), methyl methacrylate (MMA) and butyl methacrylate (BMA)) reveals interesting relations between initiator and surfactant hydrophilicity on the one hand and the hydrophilicity of the monomers on the other hand. For the water-soluble HEMA stable latexes are only obtained if hydrophobic initiators such as 2,2′-azobisisobutyronitrile or dibenzoyl peroxide in combination with alkyl sulfate surfactants with carbon chain lengths greater than 10 or surface active initiators of the 2,2′-azobis(N-2′-methylpropanoyl-2-amino-alkyl-1)-sulfonate type with alkyl chain lengths greater than 8 are employed. Stable nano size range poly(2-hydroxyethyl methacrylate) (PHEMA) particles have been prepared also by batch emulsion polymerization using ionic surface active initiators (inisurfs). The results clearly show that the formation of stable latex particles requires a proper choice of the initiator-emulsifier system regarding its hydrophilic-hydrophobic balance. The PHEMA particles prepared with surface-active initiators keep their identity and spherical shape even in the dried state whereas in the case of the other initiator-emulsifier systems complete coagulation and coalescence occurs during drying. 相似文献
74.
Darryl P. Butt Klaus S. Lackner Christopher H. Wendt Samuel D. Conzone Harriet Kung Yung-Cheng Lu Julie K. Bremser 《Journal of the American Ceramic Society》1996,79(7):1892-1898
The kinetics of simultaneous dehydroxylation and carbonation of precipitated Mg(OH)2 were studied using isothermal and nonisothermal thermogravimetric analyses. Specimens were analyzed using X-ray diffraction, transmission electron microscopy, and through measurements of the volume of carbon dioxide evolved in a subsequent reaction with hydrochloric acid. From 275° to 475°C, the kinetics of isothermal dehydroxylation in helium were best fit to a contracting-sphere model, yielding an activation energy of 146 kJ/mol, which was greater than values reported in the literature for isothermal dehydroxylation under vacuum (53–126 kJ/mol). The carbonation kinetics were complicated by the fact that dehydroxylation occurred simultaneously. The overall kinetics also could be fit to a contracting-sphere model, yielding a net activation energy of 304 kJ/mol. The most rapid carbonation kinetics occurred near 375°C. At this temperature, Mg(OH)2 underwent rapid dehydroxylation and subsequent phase transformation, whereas thermodynamics favored the formation of carbonate. During carbonation, MgCO3 precipitated on the surface of disrupted Mg(OH)2 crystals acting as a kinetic barrier to both the outward diffusion of H2 O and the inward diffusion of CO2 . 相似文献
75.
Applying a formal analysis technique to the CCITT X.509 strong two-way authentication protocol 总被引:1,自引:0,他引:1
In the quest for open systems, standardization of security mechanisms, framework, and protocols are becoming increasingly important. This puts high demands on the correctness of the standards. In this paper we use a formal logic-based approach to protocol analysis introduced by Burrows et al. [1]. We extend this logic to deal with protocols using public key cryptography, and with the notion of duration to capture some time-related aspects. The extended logic is used to analyse an important CCITT standard, the X.509 Authentication Framework. We conclude that protocol analysis can benefit from the use of the notation and that it highlights important aspects of the protocol analysed. Some aspects of the formalism need further study.This research was sponsored by the Royal Norwegian Council for Scientific and Industrial Research under Grant IT 0333.22222, and was performed while K. Gaarder was at Alcatel STK Research Centre. 相似文献
76.
Manthiou Aikaterini Klaus Phil Kuppelwieser Volker G. Reeves William 《Electronic Markets》2021,31(3):511-527
Electronic Markets - There is a growing need in the tourism and hospitality literature to harmonise service robots and artificial intelligence’s (AI) meaning and foundations, while also... 相似文献
77.
Bryan R. Moser Michael A. Jackson Kenneth M. Doll 《Journal of the American Oil Chemists' Society》2021,98(3):305-316
We report the dehydration and isomerization of renewable perillyl alcohol to industrially useful p-cymene in 91% yield utilizing 2.0 mol% para-toluenesulfonic acid (pTsOH) catalyst at 110 °C as a 3.0 M solution in toluene. Lower reaction temperatures, catalyst loadings, and/or starting concentrations resulted in lower yields of p-cymene as well as longer reaction times. Conversion of perillyl alcohol to p-cymene yielded atom and carbon economies of 88.1% and 100% as well as an E-factor of 2.7, thereby indicating that the process was both green and sustainable. A lower yield of 86% was observed when the reaction was performed neat, but a lower E-factor of 0.4 indicated that neat conditions were more desirable from an environmental perspective. Application of the optimized parameters to 3.0 M solutions of dl-limonene led predominantly to oligomerization (92%) as opposed to dehydroisomerization (5%), which was attributed to the strong Brønsted acidity of pTsOH. In addition, camphene (44%), terpinene isomers (15%), and limonene (14%) were obtained when dehydroisomerization was attempted on 3.0 M solutions of α- and β-pinene, which was once again attributed to the acidity of the catalyst. Oligomerization was strongly favored when dehydroisomerization of dl-limonene, α- and β-pinene was attempted neat. In summary, synthesis of renewable p-cymene was readily achieved from perillyl alcohol with catalytic pTsOH but competing side reactions suppressed yield when dehydroisomerization of dl-limonene, α- and β-pinene was attempted due to the strong Brønsted acidity of the catalyst. 相似文献
78.
Daniel S. Camarda Matthew J. Lampe Alan J. Lesser Philippe Desbois Klaus Stoll Claus Gabriel Rupert Konradi 《应用聚合物科学杂志》2021,138(41):51203
The creation of graft copolymers by selectively grafting a second polymer to the amorphous fraction of a semi-crystalline polymer in supercritical CO2 is demonstrated herein. The graft copolymer is synthesized by free radical polymerization of a vinyl monomer within the semi-crystalline polymer below its melt temperature. Such conditions afford selective grafting on the amorphous regions (block “B”) while leaving the crystalline domains (block “A”) unmodified. Accordingly, unique A-B, A-B-A, A-B-A-B-A, and so forth. block structures are formed. In this work, styrene is polymerized within polyamide 6, polyethylene terephthalate, and isotactic polypropylene. Purification of these material is performed to remove the un-grafted homopolymer, allowing for determination of the graft yield, the portion of polymer which covalently bonds to the semi-crystalline matrix. Grafting yields achieved in polyamide 6, polyethylene terephthalate, and isotactic polypropylene were 98%, 59%, and 15%, respectively. Property enhancements were observed upon further characterization of polystyrene-polyamide 6 copolymers, including high glass transition temperatures, the ability to be remelted, and tunable grafting molecular weight. Additionally, hydrophobicity is controlled by varying polystyrene composition. The remarkable range of accessed properties demonstrates this as a potential route to upcycling plastics. 相似文献
79.
Sascha Stanic Thomas Koch Klaus Schmid Simone Knaus Vasiliki-Maria Archodoulaki 《应用聚合物科学杂志》2021,138(28):50659
The influence of two peroxides (peroxydicarbonate/dilauroyl peroxide) with various concentrations (10–200 mmol/kg PP) and their effective opportunity to introduce long chain branched (LCB) were investigated. The dependence of a single and double extrusion step and the changes of the properties were studied. Experiments were carried out in a single screw extruder at 180°C for the first extrusion step (modification) and at 240°C for the second extrusion step (processing simulation). Melt flow rate and dynamic rheological properties were studied at a measuring temperature of 230°C. For the definitive determination of long chain branched polypropylene (LCB-PP) served the extensional rheology measurements. The mechanical properties were examined via tensile test and impact tensile test. Summarized, LCB (melt strength) could be observed via extensional rheology for all modified specimens and the mechanical properties were maintained or even improved for the modified samples. Particularly, samples containing dilauroyl peroxide display excellent mechanical properties in this study. 相似文献
80.
Chaudry Oliver Friedberger Andreas Grimm Alexandra Uder Michael Nagel Armin Michael Kemmler Wolfgang Engelke Klaus 《Magma (New York, N.Y.)》2021,34(3):367-376
Magnetic Resonance Materials in Physics, Biology and Medicine - To develop a precise semi-automated segmentation of the fascia lata (FL) of the thigh to quantify IMAT volume in T1w MR images and... 相似文献