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91.
环己烷液相无催化剂的氧化动力学研究 总被引:2,自引:0,他引:2
采用搅拌釜反应器,在确认已排除传质因素对反应速率影响的情况下,研究了环己烷液相无催化剂的氧化反应动力学。应用自由基理论及最优化计算技术,从导出的8个候选动力学模型中,确定了最佳的动力学模型,它能满意地描述环已烷氧化过程。该动力学可为环己烷氧化工业生产操作条件的优化、反应器的选型及工业设计提供依据。 相似文献
92.
李勇 《高校化学工程学报》1997,11(3):244-248
用硬链微扰理论分析了MH-55型状态方程。首次改进了该方程中的参考项,以CS硬球方程替代了原来的vanderWaals斥力项,使改进后的MH-55方程计算范围扩大到汽液两相。 相似文献
93.
Hong-Bing Tsai Da-Kong Lee Jung-Liang Liu Jiang-Wen You 《Journal of Polymer Research》1995,2(2):109-114
The block copolyetheresters with hard segments of poly(pentamethylene p,p-bibenzoate) and soft segments of poly (tetramethylene ether) were prepared by melt polycondensation of dimethyl-p,p-bibenzoate, 1,5-pentanediol and poly (tetramethyene ether) glycol (PTMEG) with molecular weights of 650, 1000 and 2000. The results by NMR indicate that the polymer composition is determined by the charge molar ratio (x) of PTMEG to dimethyl-p,p-bibenzoate. The thermal transitions of the block copolyetheresters were investigated by DSC in combination with X-ray diffraction and polarized microscopy. Some block copolyetheresters exhibit a monotropic smectic phase due to the presence of the poly (pentamethylene p,p-bibenzoate) segments. As the molar content of PTMEG increases, the average sequence length of the polyester segments decreases, the isotropic-smectic transition temperature and the smectic order decrease accordingly. When x is as high as 0.3, the block copolyetheresters exhibit no liquid crystallinity. 相似文献
94.
95.
Ping Shen Lifeng Zhang Jianxun Fu Hao Zhou Yi Wang Limei Cheng 《Ceramics International》2019,45(9):11287-11295
In the present study, the wettability between liquid iron with two different Al contents and MgOAl2O3 binary substrates was studied in reducing atmosphere. The contact angles between liquid iron with 18?ppm Al and MgO, MgO·Al2O3, Al2O3 were 133.5°, 113.7°, 126.9° respectively. With the variation of the substrate composition, the contact angles for the intermediate binary phases of the three components (MgO, MgO·Al2O3, Al2O3) obeyed the Cassie theory. In the experiment using iron with 370?ppm Al, all the contact angles were higher than that using low Al-containing iron. The surface of the iron drop was covered with an oxide layer, which mainly consisted of many small particles. With the variation of the substrate gradually from MgO to Al2O3, the composition of the oxide layer changed from MgO·Al2O3 to CaOAl2O3. The formation of the oxide layer prevented the spreading of liquid iron, leading to the increase of the contact angle. 相似文献
96.
Yasuhiko H. Mori Takehiro Nosoko Atsushi Mikami Tetsuya Ohyama 《Chemical Engineering Communications》1990,92(1):95-102
The shape of interfaces formed by the contact of two liquid phases, immiscible with each other, and a gaseous phase can be predicted on the condition that the tension to work at each interface is known with a sufficient accuracy. In general, interfacial tension data available are not so accurate, however, as to be useful as they are in predicting the shape of interfaces, particularly when the spreading coefficient of either liquid (liquid 1) on the other (liquid 2) has a negative value of a small magnitude. Presented in this note is a simple method to rectify the interfacial tension data, with the aid of a measurement of the radius of a lens of liquid 1 of a known volume placed on the horizontal surface of liquid 2, and thereby make them usable for predicting interfacial geometries. The method is tested by applying it to benzene/water and n-pentane/water systems. 相似文献
97.
A rapid test to measure performance,emission and wear of a diesel engine fueled with palm oil diesel
H. Masjuki A. M. Zaki S. M. Sapuan 《Journal of the American Oil Chemists' Society》1993,70(10):1021-1025
Results of performance, emission and tribological evaluations of palm oil methyl ester and its blends with conventional diesel
in an automobile diesel engine test bed are presented. Polymerization and carbon deposits on the fuel injector were monitored.
CO, CO2, O2, combustion efficiency and temperature of exhaust gases were also measured. Palm oil methyl ester and its blends have great
potential as alternative diesel fuel. Performance and exhaust gas emission for palm oil methyl ester and its blends with conventional
diesel are comparable with those of conventional diesel fuel. Palm oil methyl ester does not pose a severe environmental problem
and will not deteriorate engine and bearing components. 相似文献
98.
A new and effective liquid membrane process to achieve both separation and enrichment simultaneously of weak organic acids or bases was developed. The process utilizes effectively the difference in the apparent partition coefficient of the constituent species between the aqueous and organic phases, and uses the change of the apparent partition coefficients with the hydrogen ion concentration of the aqueous phase. For such a fundamental model apparatus as a diaphragm diffusion cell being operated batch wise, the effects of pK value of solutes, permeability of solutes through the membrane, volume ratio of liquids in two aqueous phases, and pH value of aqueous phase on enrichment factor and selectivity for the solute to be concentrated were discussed analytically. Separation and enrichment were demonstrated using aqueous mixed solutions of fumaric acid and L-malic acid. The results were in good agreement with the theoretical predictions. 相似文献
99.
100.
Novel side-chain liquid crystalline (LC) ionomers containing d-metals Co(II) and Ni(II) were synthesized and characterized. Both families of the ionomers are characterized by the same influence of charged group content in polymer on their phase behavior. The incorporation of 2-3 mol% of metal ions in the nematic polymer matrix leads to the induction of SmA phase and rise in the clearing point. The peculiarity of their phase behavior in comparison with the earlier investigated LC ionomers with alkaline or alkali-earth metals is the full destruction of the mesophase at the concentration of d-metal higher than 12 mol%. This phenomenon was associated with the well-known ability of the transition metal ions to form various complexes that, in the case of LC ionomers, can negatively influence the ordering of the side mesogenic groups. The proposed structure of the LC ionomers is discussed in comparison with the metallomesogenic polymer systems. 相似文献