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961.
This article will review the development of the Fe–Ga (Galfenol) alloy system for magnetostriction applications including
work on substitutional ternary alloying additions for magnetic property enhancement. A majority of the alloying addition research
has focused on substitutional ternary elements in Bridgman grown single crystals with the intent of improving the magnetostrictive
capability of the Galfenol system. Single crystals provide the ideal vehicle to assess the effectiveness of the addition on
the magnetostrictive properties by eliminating grain boundary effects, orientation variations, and grain-to-grain interactions
that occur when polycrystals respond to applied magnetic fields. In almost all cases, ternary additions of transition metal
elements have decreased the magnetostriction values from the binary Fe–Ga alloy. Most of the ternary additions are known to
stabilize the D03 chemical order and could be a primary contribution to the observed reduction in magnetostriction. In contrast, both Sn and
Al are found to substitute chemically for Ga. For Sn additions, whose solubility is limited, no reduction in magnetostriction
strains are observed when compared to the equivalent binary alloy composition. Aluminum additions, whose effect on the magnetoelastic
coupling on Fe is similar to Ga, result in a rule of mixture relationship. The reviewed research suggests that phase stabilization
of the disordered bcc structure is a key component to increase the magnetostriction of Fe–Ga alloys. 相似文献
962.
963.
Nina Georgieva Kostova Elka Kraleva Alla A. Spojakina Erika Godocikova Peter Balaz 《Journal of Materials Science》2007,42(10):3321-3325
The Al-MCM-41 has been used as support to prepare Mo-containing catalysts. The 12- molybdophosphoric heteropoly acid (HPMo)
is used as initial compound. The catalysts are synthesized by two different methods: incipient impregnation with aqueous solution
of the acid and mechanochemical synthesis. The samples were tested in the reaction of the thiophene hydrodesulfurization after
activation with mixture H2 + H2S. The effect of the preparation method of the catalysts on their physicochemical and catalytic properties has been studied.
A partial destruction of the loaded compound is observed in mechanochemically treated sample whereas the aggregates are formed
from the particles of different size in the impregnated sample. The specific surface area of the sample prepared by mechanical–chemical
treatment decreases 2–3 times, while the total pore volume is about four times lower. The HDS activity is higher on the impregnated
sample than on the mechanochemically treated one. 相似文献
964.
On structural and high temperature electrochemical properties of ZrO2 thin film coating on Zr metal produced by carbonate melt 总被引:1,自引:0,他引:1
Melt of NaCO3 can favor oxidation of Zr to form ZrO2 thin film on Zr surface, which is used to make Zr/ZrO2 oxidation/reduction electrode of pH sensor for testing elevated temperature aqueous solutions. Using SEM, EPMA, XPS, EXAFS
and HRTEM, we found that ZrO2 film is tightness and solid with 20 μm thickness composed by nanometer-sized monoclinic crystals. Zr/ZrO2 interface is characterized of zoning structure according to topography and chemical composition in five zones: oxygen-rich
ZrO2, ZrO2, oxygen-rich Zr metal, oxygen-bearing Zr and Zr from outmost to center. Melt oxidation process of Zr involved oxidation time,
air and temperature. The air is important effect on structural and electrochemical properties of ZrO2 thin film for making elevate temperature electrochemical sensor. If oxygen air largely presented in carbonate melting process,
ZrO2 thin film is not tightness and not for oxidation/reduction electrode. 相似文献
965.
Z. Ferhat-Hamida H. Phuong-Nguyen P. Bernazzani A. Haine G. Delmas 《Journal of Materials Science》2007,42(9):3138-3154
LLDPE samples synthesized with Ziegler–Natta (ZN) and Metallocene (MT) catalysts have been analyzed to investigate a potential
catalyst-dependent morphology and to find an explanation for the difficult processing of MT. Slow calorimetry at v = 0.02 K/min and IR at RT and in the melt are used. The differences between MT and ZN are assigned to their different composition,
MT not having the linear segments, which are present in ZN. Slow calorimetry is effectively a drawing process of the melt
with chain orientation followed by decay. The later event, characterized by an endotherm, ΔH
network, occurs at higher temperatures for MT, the presence of a regular distribution of methyl groups slowing down the process.
The rocking, gauche, bending and stretching regions of the IR spectra are analyzed. The nascent MT has more strained bands
in the rocking region. The wagging region reveals the more homogeneous environment of MT through the maximum absorbance at
1,368 cm−1. Decomposition of bands is made for the rocking and wagging regions. The orthorhombic crystallinity, αc (FTIR), measures the sum of long- and short-range orthorhombic order, the latter being obtained by αc (FTIR)-αc (X-rays). The values of αc (FTIR) for MT and ZN are very similar in conditions of equilibrium. The justifications for the molecular origin of ΔH
network are presented: (i) the slow relaxation of long chains strained and oriented in the melt measured by other techniques, (ii)
The correlation, for gels of a linear sample, made in different solvents, between the maximum drawability, λmax, and ΔH
network in a slow T-ramp. The range is 80–270 for λmax and 40–120 J/g for ΔH
network. (iii) The comparison of two traces of the same sample, between 140 °C and 270 °C, show that comparable events in the melt
appear in the integrated absorbance and in the slow calorimetry signal. Analysis on thin films of the little-studied CH2 stretching region reveals that their extinction coefficient, ε, and the shape of the bands are highly sensitive to the sample
history, ε diminishing by a large factor in slowly crystallized samples. Events in the slow T-ramp, followed by a fast crystallization, on the other hand, leads to materials with standard characteristics. Slow calorimetry
traces display more events (endothermic and exothermic) for MT than for ZN, a finding consistent with more flow irregularities
during processing. Equilibrium conditions and better processing could be reached for MT by extending time in the melt or using
higher temperatures. 相似文献
966.
Daniel X. Gouveia Odair P. Ferreira Antonio G. Souza Filho M. G. da Silva J. A. C. de Paiva Oswaldo L. Alves Josué Mendes Filho 《Journal of Materials Science》2007,42(2):534-538
The thermal decomposition properties of Mg–Fe hydrotalcites were studied through in situ 57Fe Mössbauer spectroscopy and in situ X-ray diffraction. Abrupt changes in the quadrupolar splitting measured in the Mössbauer spectra revealed a phase transition from the starting lamellar structure to a new crystalline arrangement. By analyzing the Mössbauer parameters we show that the material is highly disordered in the 300–400 °C temperature range. This hypothesis is confirmed by the X-ray results whose diffractograms indicated the collapse of the lamellar structure and the formation of a solid solution. 相似文献
967.
Christian P. Romero Jonathan I. Avila Edgardo Cisternas Guerau B. Cabrera Alejandro L. Cabrera Kristiaan Temst Margriet J. Van Bael 《Journal of Materials Science》2007,42(18):7667-7672
Hydrogen desorption curves were obtained from a sample composed of a square arrangement of Co dots with average diameter of
4.4 μm, separated by a distance of 11.6 μm. A macroscopic sample of Co dots grown on a 2.5 × 2.5 cm Si substrate was made
by standard lithographic techniques and used in these experiments. Thermal programmed desorption (TPD) was performed under
ultra-high vacuum conditions. Hydrogen TPD curves were obtained from a 1 × 1 cm Co dots samples displaying a maximum of intensity
at 425 K. Hydrogen TPD curve was also obtained from 1 cm× 1 cm samples of Co films and Co foils for comparison. The hydrogen
TPD curves have decreasing intensity from the Co foils to the Co dots and finally to the Co films. This indicates that there
are more sites for hydrogen adsorption on the Co dots than in the Co films. This is a surprising result because there is approximately
8.7 times less Co atoms exposed in the Co dots that in the Co film sample. A desorption energy of 27 kcal/mol was obtained
for the Co dots suggesting that hydrogen is adsorbed on an hcp hollow site of the Co dot crystalline structure. 相似文献
968.
I.H. Song 《Thin solid films》2007,515(19):7598-7602
This paper is a report on the effect of a single perpendicular grain boundary on the hot-carrier and high current stability in high performance polycrystalline silicon (poly-Si) thin film transistors (TFTs). Under a hot carrier stress condition (Vg = Vth + 1 V, Vd = 12 V), the poly-Si TFT with a single grain boundary is superior to the poly-Si without any grain boundary because of the smaller free carriers available for electric conduction. The shift of transconductance in poly-Si TFT with a single grain boundary is less than 5% after hot carrier stress during a period of 1000 s. The shift of transconductance is about 25% in the case of the poly-Si TFTs without a grain boundary in the channel. On high current stress, the poly-Si TFT without the grain boundary is less degraded than the poly-Si TFT with the grain boundary because the concentrated electric field near the drain junction is lower. 相似文献
969.
A consistent analytical model of nonlinear ion drift spectrometry for modern gas analyzers is developed. A procedure for determining the field dependence of the ion mobility using the experimental data is described. An ionogram is calculated for the case of a flat drift chamber and polynomial character of the field dependence of the ion mobility. 相似文献
970.
C. B. Winkelmann E. Collin Yu. M. Bunkov H. Godfrin 《Journal of Low Temperature Physics》2004,135(1-2):3-14
We report systematic measurements of the response of a Vibrating Wire Resonator (VWR) in normal and superfluid liquid 3He. Special attention has been paid to the hydrodynamic regime of the superfluid B-phase, where the response parameters of the VWR do not follow a simple law. We show that a simple interpolation between the region where first order slip-corrections can be applied and the ballistic regime is insufficient. Measuring an empirical effective viscosity, we propose a temperature calibration method which allows the use of VWRs as a secondary thermometer at intermediate and high pressures in the temperature range 0.2 T c < T < 50 mK. 相似文献