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51.
Using a Debye function analysis, the presence of icosahedral and face centered cuboctahedral gold in a 1 1 ratio has been found in freshly prepared Au/Mg(OH)2 catalyst. The results support earlier studies which suggest the icosahedral form to be more stable at small nanometer sizes. Interactions between the gold and the Mg(OH)2 support appear to be weak, with the gold rapidly coagulating over a period of three months. Re-analysis of the aged sample shows the gold to be mainly in the form of truncated decahedra. 相似文献
52.
以陶瓷纤维纸片为基材,顺次经水玻璃、酸性钛盐溶液浸渍共沉淀制得新型陶瓷基钛掺杂硅胶块体吸附剂.多孔介质表面分析显示:掺杂硅胶孔径在0.5~6 nm范围,以中孔为主.Fourier变换红外谱在波数954 cm 1处的特征吸收峰表明吸附剂中形成了Si-O-Ti键.根据掺杂前后固体魔角核磁共振硅谱中硅原子化学位移的变化(向高场方向移动)及X射线光电子能谱中各原子结合能的变化(Ti2p3/2的结合能随钛含量的增加而增加,而Si2p,O1s的结合能则呈相反趋势)进一步表明:钛原子替代硅原子进入硅胶网络.热重分析及烧结实验结果显示:钛掺杂吸附剂具有更好的热稳定性.新型吸附剂优异的吸附性能除了与其高的比表面积相关外,还与Ti-O键对水分子的亲合力紧密相关,其耐热性能增强与形成高热稳定性Ti-O Si键及材料表面导热性能提高有关. 相似文献
53.
Atar Musa Keskin Hakan Güçlü Yavuzcan H. 《Journal of Coatings Technology and Research》2004,1(3):219-224
The impacts of impregnation and bleaching on the varnish layer hardness of Oriental beech (Fagus orientalist L.) wood were investigated. A number of bleaching combinations {[NaOH−H2O2], [NaOH−Ca(OH)2−H2O2], [NaOH−MgSO4−H2O2] [NaHSO3−H2C2O4], [NaSiO3−H2O2], [KMnO4+NaHSO3+H2O3]} were applied at 18% concentration for bleaching to both impregnated and unimpregnated specimens of Oriental beech wood.
Subsequently, water-based (WB) varnish was coated over the samples and the varnish layer hardness values were determined in
accordance with ASTM D 4366-95.
All of the chemicals used for bleaching reduced the surface hardness. However, after varnish coating, the hardness of most
samples was similar to that of the varnish-coated natural (control) samples. 相似文献
54.
Saleh Al-Sayari Albert F. Carley Stuart H. Taylor Graham J. Hutchings 《Topics in Catalysis》2007,44(1-2):123-128
The preparation of Au/ZnO and Au/Fe2O3 catalysts using two coprecipitation methods is investigated to determine the important factors that control the synthesis
of high activity catalysts for the oxidation of carbon monoxide at ambient temperature. In particular, the factors involved
in the preparation of catalysts that are active without the need for a calcination step are evaluated. The two preparation
methods differ in the manner in which the pH is controlled during the precipitation, either constant pH throughout or variable
pH in which the pH is raised from an initial low value to a defined end point. Non-calcined Au/ZnO catalysts prepared using
both methods are very sensitive to pH and ageing time, and catalysts prepared at a maximum pH = 5 with a short ageing time
(ca. 0–3 h) exhibit high activity. Catalysts prepared at higher pH give lower activity. However, all catalysts require a short
operation period during which the oxidation activity increases. In contrast, the calcined catalysts are not particularly sensitive
to the preparation conditions. Non-calcined Au/Fe2O3 catalysts exhibit high activity when prepared at pH ≥ 5. Calcined Au/Fe2O3 prepared using the controlled pH method retain high activity, whereas calcined catalysts prepared using the variable pH method
are inactive. The study shows the immense sensitivity of the catalyst performance to the preparation methods. It is therefore
not surprising that marked differences in the performance of supported Au catalysts for CO oxidation that are apparent in
the extensive literature on this subject, particularly the effect of calcination, can be expected if the preparation parameters
are not carefully controlled and reported. 相似文献
55.
Laura Prati Alberto Villa Francesca Porta Di Wang Dangsheng Su 《Catalysis Today》2007,122(3-4):386-390
The liquid phase oxidation of glycerol with oxygen has been studied using mono and bimetallic catalysts based on Au and Pd metals supported on activated carbon, in order to study the effect of the metal on the distribution of the products and on activity of catalysts. It was found that by using bimetallic catalysts (Au–Pd) a strong synergistic effect was shown. By using a preformed nucleating centre we were able to obtain a single alloyed phase, which allowed us to address the synergistic effect to the presence of alloyed Au/Pd. The advantage of using this latter catalyst lies not only in the high activity but also in a prolonged catalyst life. Although a partial leaching of palladium and assembling of the particles have been revealed by ICP and HRTEM respectively, activity after 10 re-cycles decreased less than expected (about 10%). 相似文献
56.
58.
59.
Ruojun Lao Lihua Wang Ying Wan Jiong Zhang Shiping Song Zhizhou Zhang Chunhai Fan Lin He 《International journal of molecular sciences》2007,8(2):136-144
In this work, we reported the investigation on the interaction between DNA strands self-assembled at gold electrodes and an electron transfer protein, cytochrome c. We observed that cytochrome c exhibited well-defined electrochemistry in both double-stranded and single-stranded DNA films. This suggested that the electron transfer reaction of cytochrome c arose possibly due to the electron hopping along DNA strands rather than wiring along the double helix. We also compared the heterogeneous electron transfer rate of cytochrome c with that of a ruthenium complex, which further confirmed this mechanism. 相似文献
60.
Enhancement of the basic properties of the X zeolite with FAU framework has been carried out during synthesis, without further treatment such as ion-exchange or impregnation. Control of the washing stage enables retention of the optimum amount of alkaline hydroxides, which increases the basic catalytic activity of X zeolite in the alkylation of toluene. This alkaline hydroxides neither affect the FAU framework nor the silicon/aluminium molar ratio of the X zeolite. The optimum (Na + K)/Al molar ratio of the improved catalyst was 1.06 corresponding to a washing volume of 200 mL. This X zeolite presented better catalytic activity than a cesium-zeolite prepared by ion-exchange. The presence of hydroxysodalite impurity in the X zeolite increased the amount of impregnated alkaline hydroxides but not the catalytic activity. The present study shows that it is possible to increase the basic properties of the X zeolite directly in the synthesis process. 相似文献