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61.
采用透射电子显微术(TEM),研究了用磁控溅射技术在柔性金属基体上制备的、钇稳定的ZrO2(YSZ)为过镀层的YBa2Cu3O7-y(YBCO)薄膜的横断面结构。所得YBCO膜的超导临界转变温度Tc为91K,临界电流密度Jc=2×103A/cm2(77K,0T)。基体为Ni基合金(HasteloyC)。YSZ层为致密、均匀的细晶组织,约12μm厚,具有织构取向,并与基体紧密连接。YBCO层的厚度不均匀,约500nm;YBCO/YSZ界面有时连接较差,在该界面上有杂质出现,杂质有可能引发裂纹。 相似文献
62.
《Surface and interface analysis : SIA》2003,35(6):544-547
We have developed multiple short‐period delta layers as a reference material for SIMS ultra‐shallow depth profiling. Boron nitride delta layers and silicon spacer layers were sputter‐deposited alternately, with a silicon spacer thickness of 1–5 nm. These delta‐doped layers were used to measure the sputtering rate change in the initial stage of oxygen ion bombardment. A significant variation of sputtering rate was observed in the initial 3 nm or less. The sputtering rate in the initial 3 nm was estimated to be about four times larger than the steady‐state value for 1000 eV oxygen ions. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
63.
《Electroanalysis》2005,17(11):953-958
An electron transfer reaction between ascorbic acid (H2A) in an aqueous solution and oxidizing agent in an organic solution immiscible with water has been studied by thin‐layer cyclic voltammetry (TLCV) for charge transfer at the interface between two immiscible electrolyte solutions (ITIES). As an antioxidant, H2A provide electrons through the aqueous/organic interface to reduce Fc+ and the procedure has been proved to be a one electron process again. In this work, the first combination of TLCV and scanning electrochemical microscopy (SECM) was achieved and showed a reasonable agreement between the results from the two different approaches. Otherwise, lower concentration ratios Kr of aqueous to organic reactants was adopted, which is given as evidence to the proposed procedure of Barker. 相似文献
64.
V. G. Nefedov O. A. Artyushenko E. V. Kashevarova 《Russian Journal of Electrochemistry》2006,42(6):638-642
Mass transfer to a horizontal electrode during electrolytic evolution of oxygen and hydrogen at current densities of 100 to 10 000 A/m2 is studied. The mass transfer intensity is evaluated from the diffusion layer thickness, which varies from 60 to 5 μm at such current densities. Calculations show that the decrease in the diffusion layer thickness is due to bubbles with a stationary interphase surface crossing the diffusion layer. During the hydrogen evolution, the diffusion layer thickness is nearly the same for vertical and horizontal electrodes. During the oxygen evolution, the diffusion layer is much thinner for a horizontal electrode. Additional decrease of the diffusion layer thickness during the evolution of oxygen is associated with the lesser solution density in the near-electrode layer and with its transport away by means of natural convection. 相似文献
65.
A simple, rapid, cost-effective and accurate high performance thin layer chromatographic method has been developed for quantification
of valerenic acid in Valeriana jatamansi and Valeriana officinalis which is one of the stable compounds of Valeriana officinalis and designated as a key marker compound. Valerenic acid makes substantial contribution to the sedative and spasmolytic activity
of the essential oil and extract of Valeriana officinalis. Separation and quantification was achieved by HPTLC using ternary mobile phase of hexane: ethyl acetate: acetic acid (80:20:0.5
v/v) on precoated silica gel 60F254 aluminium plates and densitometric determination was carried out after derivatization with anisaldehyde-sulphuric acid reagent
at 700 nm, in absorption-reflectance mode. The calibration curves were linear in the range of (500 ng–2.5 μg). This is the
first HPTLC report for the identification and quantification of valerenic acid in Valeriana jatamansi and Valeriana officinalis. 相似文献
66.
生物质在流化床中的空气-水蒸气气化研究 总被引:22,自引:6,他引:22
以流化床为反应器,对生物质的空气-水蒸气气化特性进行了研究。考察了一些主要参变量,如温度 (700 ℃~900 ℃)、水蒸气/生物质比(0~4.04)、空气当量比(0.19~0.27)以及生物质粒度(0.2 mm~0.9 mm)等对气化结果的影响。在实验研究的条件范围内,生物质产气率在1.43 m3/kg~2.57 m3/kg范围内变化,产气的低热值在6 741 kJ/m3~9 143 kJ/m3范围内变化。实验结果表明:较高的气化温度有利于氢的产生;但气化温度过高会使气体热值下降;与常规的空气气化相比,水蒸气的加入使生物质气化产气率显著提高,但水蒸气加入量过多使气化温度下降,产气率和产气热值降低;生物质颗粒粒度的大小对产气组分的分布和产气率均有影响,较小颗粒的生物质会产生较多的CH4、CO和较少的CO2。 相似文献
67.
Ogbonnaya Ofor 《Journal of colloid and interface science》1996,180(2):323
Using “pure” natural hematite selected from a high silica Nigerian hematitic ore, oleate adsorption densities at the hematite–water interface were determined in the presence of various inorganic ions (anions and cations) of different charges and at varying concentrations. Adsorption density was determined using electrical conductivity measurements. The specific surface area of the hematite particles was determined using the method of adsorption of paranitrophenol in aqueous solution. Inorganic ions in solution depressed oleate adsorption at the aqueous hematite surface. The charge of the ion proved to be the dominant factor determining the depression of oleate adsorption. Ionic strength also was an influence, up to a limiting value at which monolayer oleate coverage of the hematite surface occurred. The inorganic ions in solution are considered to function through nonspecific adsorption in the diffuse region of the electric double layer. 相似文献
68.
69.
70.
The structure of the double electric layer (DEL) on a liquid dropping Sn-Ga electrode containing 8 at. % of Sn is studied in acetonitrile (AN) solutions of electrolytes. It is shown that the transition from aqueous to AN solutions of electrolytes makes it possible to expand the region of investigation of parameters of DEL on an Sn-Ga electrode from negative charges to a zero charge and to small positive charges. As follows from the obtained data, throughout the entire interval of charges studied, an excess, as compared with an Hg electrode, chemisorption interaction (Sn-Ga)-AN is absent. It is established that the distance of the closest approach of AN dipoles to an ionic core increases upon going from Hg to Sn-Ga to Ga. The Ga, Bi-Ga, and Sn-Ga electrodes, which possess close values of the “electrochemical work function,” are used as an example to show that the metal-solvent chemisorption interaction increases with decreasing distance of the closest approach of its dipoles to the ionic core of the metal. The effect of this factor becomes stronger as the donor number of the solvent increases. 相似文献