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101.
A systematic study focusing on the effect of Niobium (Nb) doping on the structural, magnetic and magnetocaloric properties of Ba2FeMoO6 samples is presented here. The samples of interest Ba2FeMo1?xNbxO6 (0 ≤ x ≤ 0.4) were prepared using the solid state reaction method and were confirmed to possess a cubic structure with Fm-3m space group using the X-ray diffraction analysis and Rietveld refinement. A second order of ferromagnetic phase transition was recorded in both the pure as well as the Nb doped samples using the temperature dependent magnetization and Arrott plots analysis. The pristine Ba2FeMoO6 (BFMO) sample indicated a spontaneous magnetization (34.6 emu/g at 100 K) with a relatively sharp magnetic transition at the Curie temperature (TC) of 315 K as compared to the doped samples. A magnetic entropy change of 0.93 Jkg?1K?1 at an applied magnetic field of 2.5 T was measured for the pure BFMO sample. The doped BFMO samples with Mo partially substituted by Nb however, were observed to effectively modify the TC accompanied by a decrease in magnetization. The results investigated in this work suggest that the magnetic and magnetocaloric properties of the BFMO can be tailored by controlled Nb doping which is of significant importance in order to realize the numerous potential applications of the material in the magnetic refrigeration technology.  相似文献   
102.
An ideal oxygen reduction catalyst for use in fuel cells should exhibit both long-term durability and high activity. In this study, to increase the durability of highly loaded platinum- and platinum-nickel alloy catalysts possessing different types of carbon supports, a nitrogen-doped carbon shell was introduced on the catalyst surface through dopamine coating. As the catalyst surfaces were altered following shell formation, the ionomer contents of the catalyst inks were adjusted to optimise the three-phase boundary formation. Single cell tests were then conducted on these inks by applying them in a membrane electrolyte assembly. Furthermore, to confirm the durability of the catalysts under accelerated conditions, the operation was continued for 200 h at 70 °C and at a relative humidity of 100%. Transmission electron microscopy and electrochemical analysis were conducted before and after the durability tests, and the observed phenomena were discussed for catalysts bearing different types of carbon supports.  相似文献   
103.
In this work, the relationship between the structural mechanisms and macroscopic electrical properties of the Nb-modified 0.96(Bi0.5Na0.84K0.16TiO3)–0.04SrTiO3 (BNKT–ST) system were elucidated by using temperature dependent and in situ synchrotron X-ray diffraction (XRD) techniques. For the composition x?=?0.0175, a large-signal piezoelectric coefficient (Smax/Emax?=?d33*) of 735 pm?V?1 at 6?kV mm?1 was observed at room temperature. Interestingly, at a higher temperature of 110?°C, the sample still showed a large d33* of 570 pm V?1. Furthermore, the temperature-invariant electrostrictive coefficient for this sample was found to be 0.0285?m4?C?2 over the temperature range of 25–170?°C. Moreover, the energy density for x?=?0.030 sample was ~1.0?J?cm?3 with an energy storage efficiency of ?70% in the temperature range of 25–135?°C. These results suggest that the synthesized Nb-modified BNKT–ST system is promising for the design of ceramic actuators as well as capacitor applications.  相似文献   
104.
Oxidation resistance of textured Ti3AlC2 ceramics was measured in the temperature range 1273–1573?K. It was found that the oxidation was markedly anisotropic and the samples exhibited a better oxidation resistance when tested along a direction transverse to the c-axis. This behavior was attributed to the rapid diffusion of Al within its basal planes to form a passivating Al2O3 scale and it respected Ellingham diagrams. The scales formed had different compositions depending on the testing direction; this response was clearly resulting from the crystallographic orientation. Even at 1473?K after 20?h exposure, the samples tested in a direction transverse to the c-axis showed a reduced weight gain which was 45 times lower than one seen on a basal plane.  相似文献   
105.
In this work, highly transparent yttria ceramics Φ?=?55?mm in size were fabricated by a hot-pressing method with 1 at.% ZrO2 or 12 at.% La2O3 as a sintering additive. For a 4-mm-thick specimen doped with ZrO2, the in-line transmittance reaches 71.1% at 400?nm and 80.9% at 1100?nm, and the transmittance of the La2O3-doped specimen is comparable to that of the ZrO2-doped specimen. By means of the relatively low sintering temperature of 1600?°C, the present samples exhibited very fine microstructures (<2?μm), giving rise to excellent mechanical strength levels (~200?MPa). With regard to the 1 at.% ZrO2-doped specimen, the combination of high strength and high thermal conductivity (~10 W/m?K) substantially improved parameters related to the thermal shock resistance. The results of this study indicate that the hot-pressed transparent yttria ceramic doped with 1 at.% ZrO2 is optically, mechanically, and thermally suitable for high-temperature IR window applications.  相似文献   
106.
NaA zeolite membranes were synthesised in the secondary growth hydrothermal method based on the seeding of the inner surface of a ceramic α-alumina tube. The impacts of crystallisation time and zeolite precursor concentration (in H2O) were investigated. The structure and stability of the prepared NaA zeolite membranes were also investigated with operating temperatures, times and pressures. The results indicate that the optimal synthesis gel molar composition was 3Na2O: 2SiO2: Al2O3: 200H2O. This led to cubic-shaped NaA zeolite which showed good stability. The optimal NaA zeolite membrane had H2O and CH3OH fluxes of 2.77 and 0.19 kg/m2h, with H2O/H2 and CH3OH/H2 separation factors of ∞ and 0.09 at a temperature of 30 °C. The NaA zeolite membrane had high thermal stability, but poor separation performance at high temperature (240 °C). The results suggested that the H2 permeation flux is significantly influenced by preferential adsorption of vapour in the NaA zeolite membrane.  相似文献   
107.
Perovskite ferroelectrics possess the fascinating piezoelectric properties near a morphotropic phase boundary, attributing to a low energy barrier that the results in structural instability and easy polarization rotation. In this work, a new lead-free system of (1-x)BaTiO3-xCaHfO3 was designed, and characterized by a coexistence of ferroelectric rhombohedral-orthorhombic-tetragonal (R-O-T) phases. With the increase amount of CaHfO3 (x), a stable coexistence region of three ferroelectric phases (R-O-T) exists at 0.06  x  0.08. Both large piezoelectric coefficient (d33~400 pC/N), inverse piezoelectric coefficient (d33*~547 pm/V) and planar electromechanical coupling factor (kp~58.2%) can be achieved for the composition with x = 0.08 near the coexistence of three ferroelectric phases. Our results show that the materials with the composition located at a region where the three ferroelectric R-O-T phases coexist would have the lowest energy barrier and thus greatly promote the polarization rotation, resulting in a strong piezoelectric response.  相似文献   
108.
Carbon contamination from the carbon paper/dies during spark-plasma-sintering (SPS) processing was examined in the MgAl2O4 spinel. The carbon contamination sensitively changes with the heating rate during the SPS processing. At the high heating rate of 100 °C/min, the carbon contamination having organized structures occurred over almost the entire area from the surface to deep inside the SPSed spinel disk. In contrast, at the slow heating rate of 10 °C/min, the carbon contamination having disordered structures occurred only around the surface area. The carbon phases transform into high pressure CO/CO2 gases by post-annealing in air and lead to pore formation along the grain junctions. The pore formation significantly occurs at the high heating rate due to the large amount of the contaminant carbon phases. This suggests that if once the carbon contamination was formed in the materials, it is very difficult to remove the carbon phases from the materials.  相似文献   
109.
Food-grade titanium dioxide (TiO2) is a common and widespread food additive in many processed foods, personal care products, and other industrial categories as it boosts the brightness and whiteness of colours. Although it is generally recognised as safe for humans, there is a growing interest in the health risks associated with its oral intake. This study quantified and identified TiO2 nanoparticles present in confectionery foods, which are children’s favourite foods, with inductively coupled plasma optical emission spectrometry (ICP-OES) and transmission electron microscopy (TEM). A reliable digestion method using hot sulphuric acid and a digestion catalyst (K2SO4:CuSO4 = 9:1) was suggested for titanium analysis. Validations of the experimental method were quite acceptable in terms of linearity, recoveries, detection limits, and quantification limits. Of all the 88 analysed foods, TiO2 was detected in 19 products, all except three declared TiO2 in their labelling. The mean TiO2 content of candies, chewing gums, and chocolates were 0.36 mg g?1, 0.04 mg g?1, and 0.81 mg g?1, respectively. Whitish particles isolated from the confectionery foods were confirmed as TiO2 nanoparticles via TEM and energy dispersive X-ray spectroscopy (EDX), in which nanosized particles (<100 nm) were identified.  相似文献   
110.
A series of branched poly(biphenylene-co-sulfone) ion exchange membranes containing perfluorocyclobutane groups were prepared for fuel cells. Two bifunctional trifluorovinyloxy-terminated monomers (sulfonable 4,4′-bis(trifluorovinyloxy)biphenyl and insulfonable 4,4′-sulfonyl-bis(trifluorovinyloxy)biphenyl) and a trifunctional trifluorovinyloxy-terminated branching agent (1,1,1-tris(4′-trifluorovinyloxyphenyl)ethane) were synthesized and terpolymerized via thermal [2π + 2π] cyclodimerization to obtain partially fluorinated and branched polymers containing 0–5 mol% of the branching agent. They were then postsulfonated by chlorosulfonic acid at room temperature, cast as membranes, and characterized to evaluate their electrochemical properties for fuel cell applications. As the branching agent content was increased, their polydispersity values highly increased, indicating they became highly branched. It was confirmed that higher branching agent content also increased the ion exchange capacity, water uptake, and proton conductivity of the branched ion exchange membranes containing perfluorocyclobutane groups. This indicates that their electrochemical properties can be easily controlled by the degree of branching. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48373.  相似文献   
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