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991.
坦克装甲车辆用橡胶履带板的研究开发 总被引:1,自引:0,他引:1
探讨了坦克装甲车辆用橡胶履带板(TTRP)的损坏摸式及其机理,从胶料配合,性能测试等方面评 TTRP的研究开发进展,并对我国TTRP的研究提出了建议。 相似文献
992.
Hale Sutcu 《Korean Journal of Chemical Engineering》2007,24(5):736-741
Pyrolysis of peat obtained from Yeniça?a, Bolu, Turkey was conducted in a fixed-bed tube furnace under various conditions, and variations in the structure of the char, tar and gas products were examined. The chars produced were studied by proximate and ultimate analyses. The maximum tar yield of 20.41% was obtained at a heating rate of 20 °C/min, a temperature of 450 °C, a sweeping gas flow rate of 100 ml/min and a 0.5–2.0 mm size range. The chemical composition of the tar was examined by elemental analysis, FTIR spectroscopy, 1H-NMR spectroscopy and column chromatography. The chemical composition of the tar with dense aliphatic structure was established to be CH1.22O0.25N0.02. The composition of the gases obtained at a heating rate of 20 °C/min for the 0.5–2.0 mm size range was examined by gas chromatography. 相似文献
993.
通过研究日用陶瓷材料在制备过程中发生的物理化学变化和最终产品的显微结构,得出日用低温陶瓷材料的制备原理,即在较低的温度下和较短的时间内完成制备日用陶瓷材料所需的物理化学变化,使制得的材料致密、均匀。具体的相抬构为,呈骨架状的晶体、填充在骨架中的玻璃相和均匀分布的由玻璃相连接的其他相。 相似文献
994.
995.
Yongwon Seo Sung-Ho Jo Ho-Jung Ryu Hee Dal Bae Chong Kul Ryu Chang-Keun Yi 《Korean Journal of Chemical Engineering》2007,24(3):457-460
A bubbling fluidized bed reactor was used to study CO2 capture from flue gas by using a potassium-based solid sorbent, sorbKX35 which was manufactured by the Korea Electric Power
Research Institute. A dry sorbent, sorbKX35, consists of K2CO3 for absorption and supporters for mechanical strength. To increase initial CO2 removal, some amount of H2O was absorbed in the sorbent before injecting simulated flue gas. It was possible to achieve 100% CO2 removal for more than 10 minutes at 60°C and a residence time of 2 s with H2O pretreatment. When H2O pretreatment time was long enough to convert K2CO3 of sorbKX35 into K2CO3 · 1.5H2O, CO2 removal was excellent. The results obtained in this study can be used as basic data for designing and operating a large scale
CO2 capture process with two fluidized bed reactors.
This work was presented at the 6
th
Korea-China Workshop on Clean Energy Technology held at Busan, Korea, July 4–7, 2006. 相似文献
996.
Viscoelastic, Thermal and Mechanical Properties of Dicyclopentadiene Bisphenol Diyanate Ester / Epoxy Co-polymers 总被引:1,自引:0,他引:1
Summary Dicyanate ester containing dicyclopentadiene cycles and epoxy co-polymers were prepared by copolymerization between epoxy
and dicyclopentadiene bisphenol cyanate esters (DCPDCE). Viscoelastic properties of the co-polymers were characterized by
the technique of dynamic mechanical analysis (DMA), which indicated that the introduction of E51 in the co-polymers would
effectively improve the toughness of DCPDCE, while the thermal dimensional stability would be weakened. Results from thermogravimetric
analysis (TGA) are in good accordance with the Tg values from DMA curves. Mechanical testing of the cured co-polymers shows that E51 can improve the mechanical properties
of the co-polymers while its usage is controlled among 5% to 15%. 相似文献
997.
Hongcang Zhou Baosheng Jin Zhaoping Zhong Yaji Huang Rui Xiao Youfei Zheng 《Korean Journal of Chemical Engineering》2007,24(3):489-494
The coal partial gasification catalyzed by limestone, sodium carbonate and dolomite was studied using a bench-scale atmospheric
fluidized bed in the presence of air and steam at 900 °C. The effects of limestone, sodium carbonate and dolomite on composition,
heating value, gas yield of product gas and carbon conversion in the catalytic coal partial gasification have been examined.
The experimental results show that the catalysts can effectively improve the gas quality, the heating value and the gas yield
of product gas and carbon conversion. The catalytic effect of sodium carbonate is better than that of limestone and dolomite.
The increase of limestone loading can enhance the quality of product gas, such as the content of combustible gas, the high
heating value and the gas yield, during coal partial gasification.
This work was presented at the 6
th
Korea-China Workshop on Clean Energy Technology held at Busan, Korea, July 4–7, 2006. 相似文献
998.
999.
Bin Li Chang-Rui Zhang Si-Qing Wang Feng Cao Yong-Gang Jiang 《Refractories and Industrial Ceramics》2007,48(4):280-283
A new wave-transparent composite reinforced by silica fibers with a hybrid matrix comprising BN and Si3N4 was prepared by precursor infiltration and pyrolysis, and it was heat-treated at elevated temperatures. The variations of
the composite during heat treatments were characterized and investigated by Fourier transform infrared spectroscopy (FT-IR),
X-ray diffraction (XRD) and scanning electron microscopy (SEM). The as-received composite exhibits good mechanical properties,
and it is almost amorphous. When treated at 1600°C, it turned brittle, and silica fibers in it were fused; the composite showed
a good crystalline form. When treated at 2100°C, the composite broke into pieces, and the composition showed only BN. Si3N4 was decomposed, and silica fibers were volatilized. The presence of BN probably affected the phase transitions of silica
fibers.
__________
Translated from Novye Ogneupory, No. 8, pp. 49–52, August 2007. 相似文献
1000.
Carbon/carbon composites were made through the pyrolysis of stabilized PAN felt and phenolic resin with the addition of 5 or 10 wt % carbon black to the matrix and then heat treatment at 600–2500°C. The effects of adding carbon black to the matrix precursor on the physical properties, microstructure, and mechanical properties of the resultant composites were investigated. Adding carbon black not only reduced the weight loss but also limited the shrinkage of the resultant composites. Adding carbon black also accelerated the formation of carbon basal planes in the matrix. At 2500°C, the crystalline stacking height in the composite with 10 wt % added carbon black was 200% greater than that with no additive. The flexural strength of the composite also increased from 15 to 42 MPa (almost 300%). © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 333–337, 2006 相似文献