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61.
The main contribution of the present article consists of new 3D parallel and symmetric thinning schemes which have the following qualities: They are effective and sound, in the sense that they are guaranteed to preserve topology. This guarantee is obtained thanks to a theorem on critical kernels; They are powerful, in the sense that they remove more points, in one iteration, than any other symmetric parallel thinning scheme; They are versatile, as conditions for the preservation of geometrical features (e.g., curve extremities or surface borders) are independent of those accounting for topology preservation; They are efficient: we provide in this article a small set of masks, acting in the grid ?3, that is sufficient, in addition to the classical simple point test, to straightforwardly implement them. 相似文献
62.
In this paper, deformation and breakup under simple shear of single molten polymer drops in a polymer matrix were investigated. Flow visualization was carried out in a Couette‐Flow apparatus under relatively high shear rates and temperatures up to 230°C. Drop/Matrix combinations were composed of polystyrene drops of 0.5–0.6 mm in diameter in polyethylene matrix, and ethylene–propylene copolymer drops of approximately the same size in polypropylene matrix. The deformation and breakup processes were studied under steady state and time‐dependent shearing conditions. Either for steady state or time‐dependant shearing conditions, drop elasticity generated at relatively high shear rates helped the drops to align perpendicular to the flow direction, i.e., parallel to vorticity axis. Also, the most striking non‐Newtonian effects for the high viscosity ratio systems were the surface erosion and the drop splitting mechanisms. The particles eroded off the main droplet surface were very fine, in the range of 10–50 μm, and led to a significant reduction in main drop size before its final breakup. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2582–2591, 2006 相似文献
63.
Michel Keddam Christiane Rakotomavo Hisasi Takenouti 《Journal of Applied Electrochemistry》1984,14(4):437-448
When the impedance is measured on a battery, an inductive impedance is often observed in a high frequency range. This inductance is frequently related to the cell geometry and electrical leads. However, certain authors claimed that this inductance is due to the concentration distribution of reacting species through the pores of battery electrodes. Their argument is based on a paper in which a fundamental error was committed. Hence, the impedance is re-calculated on the basis of the same principle. The model shows that though the diffusion process plays an outstanding role, the overall reaction rate is never completely limited by this process. The faradaic impedance due to the concentration distribution is capacitive. Therefore, the inductive impedance observed on battery systems cannot be, by any means, attributed to the concentration distribution inside the pores. Little frequency distribution is found and the impedance is close to a semi-circle. Therefore depressed impedance diagrams in porous electrodes without forced convection cannot be ascribed to either a Warburg nor a Warburg-de Levie behaviour.Nomenclature
A
D¦C¦ (mole cm s–1)
-
B
j+K¦C¦ (mole cm s–1)
-
b
Tafel coefficient (V–1)
-
C(x)
Concentration ofS in a pore at depthx (mole cm–3)
-
C
0
Concentration ofS in the solution bulk (mole cm–3)
- C C(x)
change under a voltage perturbation (mole cm–3)
- ¦C¦
Amplitude of C (mole cm–3)
-
D
Diffusion coefficient (cm2 s–1)
-
E
Electrode potential (V)
- E
Small perturbation inE namely a sine-wave signal (V)
- ¦E¦
Amplitude of E(V)
-
F
Faraday constant (96500 A s mol–1)
-
F(x)
Space separate variable forC
-
f
Frequency in Hz (s–1)
-
g(x)
KC(x)¦E¦(mole cm s–1)
-
I
Apparent current density (A cm–2)
-
I
st
Steady-state current per unit surface of pore aperture (A cm–2)
- j
Imaginary unit [(–1)1/2]
-
K
Pseudo-homogeneous rate constant (s–1)
-
K
Potential derivative ofK, dK/dE (s–1 V–1)
-
K
*
Heterogeneous reaction rate constant (cm s–1)
-
L
Pore depth (cm)
-
n
Reaction order
- P
Reaction product
-
p
Parameter forF(x), see Equation 13
-
q
Parameter forF(x), see Equation 13
-
R
e
Electrolyte resistance (ohm cm)
-
R
p
Polarization resistance per unit surface of pore aperture (ohm cm2)
-
R
t
Charge transfer resistance per unit surface of pore aperture (ohm cm2)
- S
Reacting species
-
S
a
Total surface of pore apertures (cm2)
-
S
0
Geometrical surface area
-
S
p
Developed surface area of porous electrode per unit volume (cm2 cm–3)
-
s
Concentration gradient (mole cm–3 cm–1)
-
t
Time
-
U
Ohmic drop
-
x
Distance from pore aperture (cm)
-
Z
Faradaic impedance per unit surface of pore aperture (ohm cm2)
-
Z
x
Local impedance per unit pore length (ohm cm3)
-
z
Charge transfer number
-
Porosity
-
Thickness of Nernst diffusion layer
-
Penetration depth of reacting species (cm)
-
Penetration depth of a.c. signal determined by the potential distribution (cm)
-
Electrolyte (solution) resistivity (ohm cm)
-
0
Flow of S at the pore aperture (mole cm2 s–1)
-
Angular freqeuncy of a.c. signal, 2f(s–1)
-
Integration constant 相似文献
64.
Sara Cavaliere-Jaricot Arnaud Etcheberry Michel Herlem Henri Perez 《Electrochimica acta》2007,52(6):2285-2293
Platinum nanoparticles (n-Pt), over-grafted with 2-thiophenecarbonyl chloride are assembled on gold electrodes, by the Langmuir Blodgett (LB) technique using behenic acid (BHA) as promoting agent. These layers are electrochemically active without any preliminary activation. The [Fe(CN)6]3−/4− redox couple was used as electrochemical probe. This paper reports on the influence of the number of deposited LB layers, and the n-Pt density on the electrochemical response. n-Pt density was modified by the change of the “BHA/n-Pt” ratio. Cyclic voltammograms of “[Fe(CN)6]3−/4−” were observed whatever the coating conditions. As soon as the first layer was deposited the electrochemical response was associated to the n-Pt coverage, its response slightly increased up to a steady state for five or seven layers. As expected, the increase of the Pt density favored the increase of the current density. XPS analysis performed before and after electrochemical cycling showed that 4-mercaptoaniline capped platinum nanoparticles, and their over grafting were chemically and electrochemically stable. Analysis of influence of the number or the n-Pt density of the layers showed that the electrochemically active part of LB electrodes was provided by the last layer plus a part of the underlying one. 相似文献
65.
The axial and radial distributions of solid and gas holdups were investigated in an air‐water‐glass bead circulating fluidized bed (GLSCFB) using a new ultrasonic technique, with a new method based on signal fluctuations. The cross‐sectional averaged gas and solid holdups measured at two axial positions appear to be similar at all studied operating conditions. The radial non‐uniformity decreases with increasing liquid velocity but does not change with an increasing solid circulating rate. The radial distribution of gas holdup was more uniform for 1.3 mm beads than for 433 µm glass beads. 相似文献
66.
Frédérique Rémy Thomas Flament Aurélie Michel Jacques Verron 《International journal of remote sensing》2014,35(14):5497-5512
From September 2002 to October 2010, the Envisat radar altimeter surveyed Greenland and Antarctica ice sheets on a 35 day repeat orbit, providing a unique data set for ice sheet mass balance studies. Up to 85 repeat cycles are available and the whole Envisat data set may be along-track processed in order to provide height variability and trend with a good spatial resolution for the objectives of ice sheet survey.Soon, a joint Centre National d’Etudes Spatiales/Indian Space Research Organisation mission, SARAL (Satellite with Argos and AltiKa), with the AltiKa payload on board, will be launched on exactly the same orbit (less than 1 km of the nomimal orbit in the across-track direction). This will allow an extension of previous European Remote Sensing (ERS) satellite, ERS-1 and ERS-2, and Envisat missions of the European Space Agency (ESA), in particular from the point of view of ice altimetry. However, AltiKa operates in the Ka band (36.8 GHz), a higher frequency than the classical Ku band (13.6 GHz), leading to important modifications and potential improvements in the interactions between radar wave and snow-pack.In this paper, a synthesis is presented of all available information relevant to ice altimetry scientific purposes as derived from the Envisat mission: mean and temporal derivatives of the height ? but also of the backscatter and of the two waveform parameters ? snow-pack change corrections, across-track surface slope at 1 km scale, etc. The spatial and temporal variability of ice sheet surface elevation is investigated with the help of the high-resolution Envisat along-track observations. We show that at least 50 repeat cycles are needed to reach the required accuracy for the elevation trend. It is thus advocated as potentially highly beneficial for SARAL/AltiKa as a follow-on mission. Moreover, the novel characteristics of SARAL/AltiKa are promising in improving our understanding of snow penetration impact. 相似文献
67.
The catalytic activity of Pt catalysts supported on high surface area tin(IV) oxide in the complete oxidation of CH4 traces under lean conditions at low temperature was studied in the absence and in the presence of water (10 vol.%) or H2S (100 vol.ppm). Their catalytic properties were compared to those of Pd/Al2O3 and Pt/Al2O3. In the absence of H2S in the feed, Pt/SnO2appears as a very promising catalyst for CH4 oxidation, being even significantly more active under wet conditions than the best reference catalyst, Pd/Al2O3. Catalysts steamed-aged at 873 K were also studied in order to simulate long term ageing in real lean-burn NGV exhaust conditions. To this respect, Pt/SnO2 is slightly less resistant than Pd/Al2O3. In the presence of H2S, Pt/SnO2catalysts are rapidly and almost completely poisoned, comparably to Pd/Al2O3and the catalytic activity is hardly restored upon oxidising treatment below 773 K. A synergetic effect between Pt and specific surface SnO2sites active in CH4oxidation is proposed to explain the superior catalytic behaviour of Pt/SnO2. 相似文献
68.
Pei Lian Ma Basil D. Favis Michel F. Champagne Michel A. Huneault Florin Tofan 《Polymer Engineering and Science》2002,42(10):1976-1989
Blends of polyethylene terephthalate (PET) and ethylene‐ethyl acrylate‐maleic anhydride terpolymer (E‐EA‐MAH) were dynamically crosslinked in a one‐step extrusion process. An amine‐terminated glycol reacting with MAH moieties was used as the crosslinking agent. The effect of blend composition and dynamic crosslinking on the microstructure and mechanical properties were investigated. Blend ratios ranging from 80:20 to 20:80 PET/E‐EA‐MAH were studied. The region of phase inversion was located for uncrosslinked and dynamically crosslinked blends. The rheological characterization was also carried out for these blends in comparison with the neat materials. After dynamic crosslinking, the phase inversion is shifted from the 30–40% range to the 70–80% range of elastomer content. This shift is induced by the increase of viscosity and elasticity of the network formed. Dynamically crosslinked blends show significant improvements in impact strength but also exhibit a decrease in elongation at break. 相似文献
69.
Pascale Sabin Bouchra Benjelloun-Mlayah Michel Delmas 《Journal of the American Oil Chemists' Society》1997,74(5):481-489
Two sets of alkyd resins of variable oil lengths with the required properties for offset printing ink formulations, modified
by sunflower and rapeseed oil, were synthetized according to the “monoglyceride” process. The influence of the acyl composition
of the modifying vegetable oil and of the oil content on alkyds’ properties was determined by detailed chemical and rheological
characterization. Molecular structure, size, and molecule size distribution appeared to be linked to these two factors. A
comparative study with two usual linseed oil-modified alkyds led to determination of the more appropriate alkyds for applications
in offset varnishes. 相似文献
70.
Structure and functional complementation of engineered fragments from yeast phosphoglycerate kinase 总被引:1,自引:0,他引:1
Pecorari Frederic; Minard Philippe; Desmadril Michel; Yon Jeannine M. 《Protein engineering, design & selection : PEDS》1993,6(3):313-324
Previous studies have shown that, although the isolated structuraldomains of yeast phosphoglycerate kinase recover a quasi-nativestructure in vitro as well as in vivo, they do not reassociatenor generate a functional enzyme. The aim of this work was firstto study the folding of complementary fragments different fromstructural domains and second to determine the requirementsfor their reassociation and functional complementation. Themethod used for producing rigorously defined fragments consistsof the introduction of a unique cysteinyl residue in the proteinfollowed by a specific cleavage by 5'5'-dithiobis(2-nitrobenzoate)/potassiumcyanide at this residue. Two pairs of complementary fragmentswere thus obtained, 196/97415 and 1248/249415.The structure and stabilities of the different fragments werestudied. The short fragments, i.e. 196 and 249415were found to contain some secondary structure, but to havea low stability. Each large fragment has a high structural contentand a stability close to that of the corresponding domain. Incontrast to that observed with the isolated domains, a weakbut significant complementation was observed for the two pairsof fragments; the pair of fragments 1248/249415recovered 8% of the activity of the native enzyme upon complementation.An independent refolding of the complementary fragments beforereassociation decreased the yield of complementation for thepair of fragments 196/97415, but did not affectthe complementation for the other pair (1248/249415).From the present data and previous work on the isolated domains,it appears that the correct folding of the isolated fragmentsis not a prerequisite for their complementation. 相似文献