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Correlation Between Magnetic Properties and Allotropic Phase Transition of Fe–Co–V Alloy 被引量:1
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作者 Saeed Hasani Ali Shafyei +4 位作者 Morteza Shamanian Peiman Behjati Hossein Mostaan Timu Juuti Jerzy A.Szpunar 《Acta Metallurgica Sinica(English Letters)》 SCIE EI CAS CSCD 2015年第8期1055-1058,共4页
In this study, the allotropic phase transition and its effect on the magnetic behavior of Fe Co–7 wt%V alloy were investigated. It was found that c phase is observed in the microstructure in the as-cast condition, an... In this study, the allotropic phase transition and its effect on the magnetic behavior of Fe Co–7 wt%V alloy were investigated. It was found that c phase is observed in the microstructure in the as-cast condition, and it diminishes after severe cold rolling(90% reduction). After annealing at temperatures higher than 500 up to 750 ℃, the c phase is observed in the structure, again. But, this phase is disappeared by annealing at temperatures above 750 ℃ due to the formation of vanadium-rich precipitates. Thermocalc software was used in order to elucidate the influence of vanadium percent on the stability of c phase in Fe–Co alloys. Also, magnetic studies showed that the saturation induction is reduced by annealing at temperatures from 500 up to 750 ℃, which is related to the formation of residual non-magnetic γ phase. 展开更多
关键词 Fe–Co–V alloy Thermocalc software Magnetic material phase transformation Electron backscatter diffraction(EBSD)
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Design, Synthesis and Evaluation of Substituted N-(3-Arylpropyl)-9,10-dihydro-9-oxoacridine-4-carboxamides as Potent MDR Reversal Agents in Cancer 被引量:3
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作者 Velingkar, V. S. Dandekar, V. D. 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第3期504-510,共7页
A novel class of molecules with structure N-(3-arylpropyl)-9,10-dihydro-9-oxoacridine-4-carboxamides (20- 29) were designed by generating a pharmacophore for potent MDR reversal activity using phase drug design so... A novel class of molecules with structure N-(3-arylpropyl)-9,10-dihydro-9-oxoacridine-4-carboxamides (20- 29) were designed by generating a pharmacophore for potent MDR reversal activity using phase drug design software. The designed molecules were synthesized by a novel synthesis route and evaluated for their inhibitory effects on the transport activity of P-glycoprotein (P-gp) by standard Hoechst 33342 assay method. Based on the pIC50 values of ten title compounds screened, three compounds exhibited better activity as compared to Verapamil used as standard. 展开更多
关键词 N-(3-arylpropyl)-9 10-dihydro-9-oxo-acridine-4-carboxamides MDR reversal agents pharmacophore phase drug design software structure-activity relationships structure elucidation
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