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铝基铁合金粉化影响因素分析及措施
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作者 李学慧 王东溟 +1 位作者 解斌 梁荣山 《鞍钢技术》 CAS 2024年第4期43-47,76,共6页
采用正交试验法分析了炼钢脱氧用铝基铁合金粉化的影响因素,结果表明,铝、碳、钛含量对合金抗粉化时间有不同程度的影响,而Ti/C是决定合金粉化时间的主要因素,该值达到10以上时,合金即具有较强抗粉化能力。当合金含铝量为40%~60%时,选... 采用正交试验法分析了炼钢脱氧用铝基铁合金粉化的影响因素,结果表明,铝、碳、钛含量对合金抗粉化时间有不同程度的影响,而Ti/C是决定合金粉化时间的主要因素,该值达到10以上时,合金即具有较强抗粉化能力。当合金含铝量为40%~60%时,选择碳、钛含量为B1、C4的水平性价比较高。 展开更多
关键词 炼钢脱氧 铝基铁合金 粉化时间 含量
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Combustion synthesis of FeAl−Al2O3 composites with TiB2 and TiC additions via metallothermic reduction of Fe2O3 and TiO2 被引量:2
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作者 Chun-Liang YEH Chih-Yao KE 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2020年第9期2510-2517,共8页
Combustion synthesis involving metallothermic reduction of Fe2O3 and TiO2 was conducted in the mode of self-propagating high-temperature synthesis(SHS)to fabricate FeAl-based composites with dual ceramic phases,TiB2/A... Combustion synthesis involving metallothermic reduction of Fe2O3 and TiO2 was conducted in the mode of self-propagating high-temperature synthesis(SHS)to fabricate FeAl-based composites with dual ceramic phases,TiB2/Al2O3 and TiC/Al2O3.The reactant mixture included thermite reagents of 0.6Fe2O3+0.6TiO2+2Al,and elemental Fe,Al,boron,and carbon powders.The formation of xFeAl−0.6TiB2−Al2O3 composites with x=2.0−3.6 and yFeAl−0.6TiC−Al2O3 composites with y=1.8−2.75 was studied.The increase of FeAl causes a decrease in the reaction exothermicity,thus resulting in the existence of flammability limits of x=3.6 and y=2.75 for the SHS reactions.Based on combustion wave kinetics,the activation energies of Ea=97.1 and 101.1 kJ/mol are deduced for the metallothermic SHS reactions.XRD analyses confirm in situ formation of FeAl/TiB2/Al2O3 and FeAl/TiC/Al2O3 composites.SEM micrographs exhibit that FeAl is formed with a dense polycrystalline structure,and the ceramic phases,TiB2,TiC,and Al2O3,are micro-sized discrete particles.The synthesized FeAl−TiB2−Al2O3 and FeAl−TiC−Al2O3 composites exhibit the hardness ranging from 12.8 to 16.6 GPa and fracture toughness from 7.93 to 9.84 MPa·m1/2. 展开更多
关键词 FeAl-based composites self-propagating high-temperature synthesis metallothermic reduction activation energy
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