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91.
A simple method has been devised for immobilization of acetylcholinesterase (AChE) covalent bonding to a multiwall carbon
nanotube (MWNT)-cross-linked cellulose acetate composite on a screen-printed carbon electrode (SPCE) and a sensitive and disposable
amperometric sensor for rapid determination of carbaryl pesticide is proposed. The immobilized enzyme was preserved on this
film because of the excellent biocompatibility and non-toxicity of cellulose acetate. Based on the inherent conductive properties
of the MWNT, the immobilized AChE had greater affinity for ATCl and excellent catalytic effect in the hydrolysis of ATCl.
MWNT improved the interface enzymatic hydrolysis reaction and increased the amperometric response of the sensor. Under optimum
conditions, the inhibition of carbaryl on AChE increased linearly with the increasing concentration of carbaryl in two ranges,
from 0.01 to 0.5 μg mL−1 and from 2 to 20 μg mL−1, with the correlation coefficients of 0.9985 and 0.9977, respectively. The detection limit was 0.004 μg mL−1 taken as the concentration equivalent to 10% decrease in signal. The sensor showed acceptable stability, accuracy and could
be fabricated in batches, thus it is economic and portable. This type of disposable enzyme-based amperometric sensor has extensive
application potential in environmental monitoring of pesticides. 相似文献
92.
Debasmita Das Purabi Rani Samaddar Pratik Kumar Sen Kaushik Das 《Journal of Applied Electrochemistry》2008,38(6):743-749
Galvanostatic steady state current potential measurements were carried out for oxidation of a series of aliphatic alcohols
having varying number of hydroxyl groups. The anodically deposited layer of MnO2 on platinum was used as the electrode material. The deposit was characterised by scanning electron microscopy (SEM), energy
dispersive X-ray analysis (EDAX) and electrode potential measurements. The catalytic role of MnO2 in the electro-oxidation of alcohols was indicated by the chronopotentiograms and the cyclic voltammograms. An analysis of
the electrochemical data indicated a catalytic EC mechanism in which Mn (V) is generated electrochemically and consumed chemically
in succession. Based on this and the hydrogen bonding interaction between alcoholic hydroxyl groups and MnO2 layer, a mechanism was proposed which accounts for the variation in the observed electrochemical reaction orders. Tafel behaviour
was found to be followed only approximately. Current efficiency of the electrochemical oxidation of polyols was studied. Replacement
of platinum by carbon as current collector was found to leave the electrocatalytic activity of the MnO2 deposit practically unaltered. 相似文献
93.
Teresa Łuczak 《Journal of Applied Electrochemistry》2008,38(4):469-476
The electrooxidation of phenylethanolamine (2-amino-1-phenylethanol) at a gold electrode in alkaline electrolyte has been
studied. Measurement of the differential capacitance of the electric double layer versus the electrode potential has shown
that the adsorption of phenylethanolamine at the gold-solution interface plays a significant role in the oxidation mechanism.
The effect of amine concentration, electrolyte pH and potential scan rate on the electrooxidation is analysed. 相似文献
94.
S. Zisekas G. Karagiannakis C. Kokkofitis M. Stoukides 《Journal of Applied Electrochemistry》2008,38(8):1143-1149
The reaction of NH3 decomposition was studied on Ag in a proton conducting double chamber cell-reactor. The proton conductor was a strontia-ceria-ytterbia
(SCY) perovskite of the form SrCe0.95Yb0.05O3−α. The reaction was studied at 350–700 °C and atmospheric total pressure. The proton transference number (PTN) was calculated
by simultaneous measurement of the imposed current and the proton flux and it was found to vary between 0.5 and 0.7. The effects
of imposed current, temperature and inlet gas composition on the reaction rate and the PTN, were examined. Although the faradaic
efficiency (Λ) remained near unity in all experiments, reaction rate enhancements (ρ) as high as 57 were achieved. An up to
90% decrease in the activation energy of the reaction was observed when protons were electrochemically “pumped” away from
the catalyst. 相似文献
95.
Kiyoaki Imoto Kohshin Takahashi Takahiro Yamaguchi Teruhisa Komura Jun-ichi Nakamura Kazuhiko Murata 《Solar Energy Materials & Solar Cells》2003,79(4):459-469
Here, we reported that a new carbon electrode prepared with an activated carbon was superior to a Pt sputtered electrode as the counter electrode of dye-sensitized solar cells. The photovoltaic performance was largely influenced by the roughness factor of carbon electrode. The open-circuit voltage increased by about 60 mV using the carbon counter electrode compared to the Pt counter electrode because of positive shift of the formal potential for I3−/I− couple. 相似文献
96.
97.
The effects of soaking of whole, dehulled and ground millet and soybean seeds on phytate degradation and Phy/Fe and Phy/Zn molar ratios 总被引:1,自引:0,他引:1
Isabelle Lestienne Claire Mouquet-Rivier Christèle Icard-Vernière Isabelle Rochette & Serge Trèche 《International Journal of Food Science & Technology》2005,40(4):391-399
The degradation and leaching of phytates, phytase activity and iron and zinc concentrations have been studied after soaking of whole seeds, dehulled seeds and flours of millet and soybean, in order to investigate the efficiency of soaking on reducing Phy/Fe and Phy/Zn molar ratios. When using millet grains, dehulling and milling before soaking facilitated the leaching of phytates and phytases in the aqueous medium and hence phytate degradation. Dehulling of soybean seeds led to a marked increase in phytate content, whereas milling favoured reactions between phytases and phytates. The Phy/Fe and Phy/Zn molar ratios decreased only slightly during soaking. The highest decreases for millet were obtained after soaking of flour for 8 h (Phy/Fe: 10.8–7.7 and Phy/Zn: 20.3–15.1), and after soaking of whole seeds for 24 h for soybean (Phy/Fe: 10.4–9.4 and Phy/Zn: 23.8–19.1). Cooking of flours with water used for soaking did not increase phytate degradation. 相似文献
98.
Akbar Eslami Simin Nasseri Bahram Yadollahi Alireza Mesdaghinia Foroogh Vaezi Ramin Nabizadeh Shahrokh Nazmara 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2008,83(11):1447-1453
BACKGROUND: Over the past several decades methyl tert‐butyl ether (MTBE) as additive to gasoline, intended to either boost ratings of fuel or to reduce air pollution, has been accepted worldwide. Since MTBE has high water solubility, the occurrence of fuel spills or leaks from underground storage tanks or transferring pipeline has led to the contamination of natural waters. In this study the degradation of aqueous MTBE at relatively high concentrations was investigated by a UV‐visible/ZnO/H2O2 photocatalytic process. The effects of important operational parameters such as pH, amount of H2O2, catalyst loading and irradiation time were also investigated. Concentration of MTBE and intermediates such as tert‐butyl formate and tert‐butyl alcohol were measured. RESULTS: Time required for complete degradation increased from 20 to 150 min when the initial concentration was increased from 10 to 500 mg L?1. The first‐order rate constants for degradation of MTBE were estimated to be 0.183–0.022 min?1 as the concentration increased from 10 to 500 mg L?1. Study of the overall mineralization monitored by total organic carbon analysis showed that at an initial concentration of 100 mg L?1 MTBE complete mineralization was obtained after 100 min under UV‐visible/ZnO/H2O2 photocatalysis. CONCLUSION: The data presented in this paper clearly indicated that UV‐visible/ZnO/O2 as an advanced oxidation process provides an efficient treatment alternative for the remediation of MTBE‐contaminated waters. Copyright © 2008 Society of Chemical Industry 相似文献
99.
100.
氢化物发生原子吸收光谱法测定金属锌中的痕量汞 总被引:1,自引:1,他引:0
采用氢化物发生原子吸收光谱法测定金属锌中的痕量汞,研究了金属锌消解的最佳条件,本法简便、快速、重现性好,准确度高,灵敏度为0.73μg/L,检测限为0.22μg/L,相对标准偏差为3.1%,回收率为96%-102%。 相似文献