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51.
We consider scaling of flow within a stirred tank with increasing Reynolds number. Experimental results obtained from two different tanks of diameter 152.5 and 292.1 mm, with a Rushton turbine operating at a wide range of rotational speeds stirring the fluid, are considered. The Reynolds number ranges from 4000 to about 78,000. Phase-locked stereoscopic PIV measurements on three different vertical planes close to the impeller give phase-averaged mean flow on a cylindrical surface around the impeller. The scaling of θ- and plane-averaged radial, circumferential and axial mean velocity components is first explored. A theoretical model for the impeller-induced flow is used to extract the strength and size of the three dominant elements of the mean flow, namely the circumferential flow, the jet flow and the pairs of tip vortices. The scaling of these parameters with Reynolds number for the two different tanks is then obtained. The plane-averaged mean velocity scales with the blade tip velocity above a Reynolds number of about 15,000. However, parameters associated with the jet and tip vortices do not become Reynolds number independence until Re exceeds about 105. The results for the two tanks exhibit similar Reynolds number dependence, however, a perfect collapse is not observed, suggesting a sensitive dependence of the mean flow to the finer details of the impeller. 相似文献
52.
The effects of potassium on the catalytic behavior in CO hydrogenation over K-promoted Fe/carbon catalysts having low K/Fe
ratios were investigated. Even though the doses of potassium were low the promotional effects were pronounced, especially
on the olefin-to-paraffin ratio, and theC
3
toC
4
olefin selectivities of the K-promoted catalysts were as high as 51 to 66 mol%. Over the catalysts having no or low potassium
content the olefin-to-paraffin ratio and the ratio of the CO2 formation rate to the rate of CO conversion to hydrocarbons remained roughly the same regardless of temperature, while over
the K-promoted catalysts having higher potassium content they increased with temperature. Formation of significant amounts
of filamentous carbon was observed in the K-promoted catalysts; however, the carbon deposition did not appear to affect the
inherent activity and selectivity of the K-promoted catalysts. 相似文献
53.
Novel polyimides were synthesized from 1‐[3′,5′‐bis(trifluoromethyl)phenyl] pyromellitic dianhydride (6FPPMDA) by a conventional two‐step process: the preparation of poly(amic acid) followed by solution imidization via refluxing in p‐chlorophenol. The diamines used for polyimide synthesis included bis(3‐aminophenyl)‐3,5‐bis(trifluoromethyl)phenyl phosphine oxide, bis(3‐aminophenyl)‐4‐trifluoromethylphenyl phosphine oxide, and bis(3‐aminophenyl)phenyl phosphine oxide. The synthesized polyimides were designed to have a molecular weight of 20,000 g/mol by off‐stoichiometry and were characterized by Fourier transform infrared, NMR, differential scanning calorimetry, and thermogravimetric analysis. In addition, their intrinsic viscosity, solubility, water absorption, and coefficient of thermal expansion (CTE) were also measured. The adhesion properties of the polyimides were evaluated via a T‐peel test with bare and silane/Cr‐coated Cu foils, and the failure surfaces were investigated with scanning electron microscopy. The 6FPPMDA‐based polyimides exhibited high glass‐transition temperatures (280–299°C), good thermal stability (>530°C in air), low water absorption (1.46–2.16 wt %), and fairly low CTEs (32–40 ppm/°C), in addition to good adhesion properties (83–88 g/mm) with silane/Cr‐coated Cu foils. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1801–1809, 2005 相似文献
54.
Oxidation and reduction processes on coal- and mineral-pyrite surfaces have been investigated to better understand the reactions that control the hydrophobicity and flotation behavior of pyrite. The incipient oxidation and reduction reactions were studied using fresh surfaces of pyrite that were created by in situ fracturing electrodes potentiostated at a predetermined potential. Chronoamperometry immediately after fracture and subsequent cyclic voltammetry have established that fresh fracture surfaces of pyrite instantaneously assume a unique potential (referred to as the “stable” potential) at which neither oxidation nor reduction takes place. For Peruvian and Chinese pyrites, the stable potential is −0.28 V (standard hydrogen electrode, SHE) at pH 9.2 and 0 V at pH 4.6. The initial oxidation of pyrite begins at potentials slightly positive of the stable potential and is believed to produce a hydrophobic sulfur-rich species, most likely a polysulfide or metal-deficient sulfide. A rotating ring-disc electrode (RRDE) was employed to study the kinetics and mechanisms of surface reactions on pyrite over moderate potential ranges. Two distinct soluble reduction products (ferrous hydroxide and HS−) and one distinct soluble oxidation product (ferrous hydroxide) were observed on pyrite in alkaline solutions. It is concluded that the initial oxidation of pyrite and the oxidation of ferrous to ferric hydroxide occur in a similar potential range. When the electrode is oxidized, e.g. by polishing, prior to experiments, the initial oxidation of pyrite is masked by the oxidation of ferrous hydroxide, making it difficult to study the oxidation of pyrite itself. 相似文献
55.
Drop-on-demand ink-jet inks made from dyes generally show poor light and wet fastness. A number of studies have been carried out previously to improve the fastness of such inks by introducing novel dyes and new additives. Based on the research results, use of fast dyes could give ink-jet inks with good properties. This study describes new black dyes for aqueous ink-jet inks, which show better light and wet fastness and print quality, compared to an analogous ink formulated from CI Food Black 2. 相似文献
56.
Man-Hee HanJung-Whan Kim Jinwon KimJung Yoon Ko Jules J. MagdaIn Suk Han 《Polymer》2003,44(16):4541-4546
The acrylic comonomers hydroxypropyl methacrylate (HPMA) and N,N-dimethylaminoethyl methacrylate (DMA) have been used in several earlier studies to produce pH-responsive hydrogels. However, these same monomers can also be used to prepare hydrogels that are highly responsive to temperature. One manifestation of this temperature sensitivity is a sharp decrease in hydrogel optical transparency that occurs when the temperature exceeds a critical transition value. For example, a hydrogel that exhibits a swelling transition at the physiological pH value of 7.4 has a transition temperature of about 45 °C when the environmental salt concentration is 0.15 M. The value of the transparency transition temperature is shown to depend on hydrogel synthesis parameters such as comonomer mole ratio, crosslinker mole ratio, and even initiator concentration. By reducing the mole ratio of the crosslinker tetraethylene glycol dimethacrylate (TEGDMA), the transition temperature can be lowered by as much as 15 °C. Environmental salt concentration and solvent polarity are also shown to influence the transition temperature. 相似文献
57.
The application of some polymers as nucleating agents for polypropylene has been examined. Among various polymeric nucleating agents, polycyclopentene was found to be a superior nucleating agent to typical organic nucleating agents. When polycyclopentene was added to polypropylene, the crystallization temperature and the degree of crystallinity of polypropylene increased. In addition, the crystallization rate and the number of spherulites increased whereas the size of spherulites decreased remarkably. As a result of polycyclopentene addition, the transparency of polypropylene film could be improved considerably. © 1994 John Wiley & Sons, Inc. 相似文献
58.
Min-Jae Yoon Yoan-Sang Bae Sang-Ha Son Jae-Wook Lee Chang-Ha Lee 《Korean Journal of Chemical Engineering》2007,24(5):877-880
Luminescent yttrium aluminum garnet (YAG, Y3Al5O12) nanoparticles doped with Eu (10 at%) were synthesized in batch-type and continuous-type supercritical water (SCW) reactors.
In the case of the continuous-type SCW method, the particles of YAG: Eu phosphors were much smaller and demonstrated a uniform
spherical-like shape. Inversely, in the case of the batch-type SCW method, a needle-like or elliptical-like shape was formed
because a finite amount of time was required to reach SCW conditions from ambient conditions. However, the emission intensity
of YAG: Eu phosphors synthesized by using the batch-type SCW method was stronger. Therefore, it is concluded that the continuous-type
SCW method is superior to the batch-type SCW method from the viewpoint of the particle size and shape, but the luminescence
property of phosphors in the continuous-type SCW method needs to be improved. In addition, a calcination process slightly
improved the luminescence intensities of YAG: Eu phosphors generated by using either the batch-type or continuous-type SCW
methods. 相似文献
59.
Summary New biodegradable hydrophobic polyurethane (PU)/hydrophilic poly (ethylene glycol) diacrylate (PEGDA) IPN was simultaneously synthesized with changing the molecular weight of PEGDA to investigate the effect of crosslinking density on the degree of phase separation. PU was modified using biodegradable poly(-caprolactone)diol and the hydroxy group of PEG was substituted to crosslinkable acrylate group having double bond, which induce photo-polymerization. The sturucture of PEGDA was confirmed by NMR. Because the reaction rate of PEGDA was faster than that of PU, the continuous matrix of the micro-separated PU/PEGDA IPNs having amphiphilic character was made of hydrophilic PEGDA-rich phase. All IPNs have sea-island morphology resulting from the suppressed phase separation. The effect of the degree of phase separation on blood compatibility was investigated. 相似文献
60.
Catalytic performances of various metal molybdates were tested in the oxidative dehydrogenation of propane to propene with molecular oxygen under an atmospheric pressure. Most of the molybdates tested promoted the selective oxidative conversion of propane to propene and among them cobalt and magnesium molybdates were found highest in the activity and selectivity. It was also found that their catalytic activities were highly sensitive to the catalyst composition, and it turned out that Co0.95MoO
x
and Mg0.95MoO
x
catalysts which have slightly excess molybdenum showed the highest activity in the oxidative dehydrogenation of propane. Under the optimized reaction conditions, higher reaction temperatures and lower partial pressures of oxygen, these catalysts gave 60% selectivity to propene at 20% conversion of propane. Since the molybdates having the surface enriched with molybdenum oxide tended to show high activity for the propane oxidation, surface molybdenum oxide clusters supported on metal molybdate matrix seem to be the active sites for the selective oxidative dehydrogenation of propane. 相似文献