• Honam Mathematical Journal
• /
• v.41 no.3
• /
• pp.581-593
• /
• 2019

The notions of (${\in}$, ${\in}{\vee}q$)-permeable S-value and (${\in}$, ${\in}{\vee}q$)-permeable I-value are introduced, and related properties are investigated. Relations among (${\in}$, ${\in}{\vee}q$)-fuzzy subalgebra, (${\in}$, ${\in}{\vee}q$)-fuzzy ideal, (strong) lower and (strong) upper level sets, (${\in}$, ${\in}{\vee}q$)-permeable S-value, (${\in}$, ${\in}{\vee}q$)-permeable I-value, S-energetic set, I-energetic set, right stable set and right vanished set are discussed.

• The Transactions of The Korean Institute of Electrical Engineers
• /
• v.59 no.2
• /
• pp.445-451
• /
• 2010

This paper presents a threshold adaptation based voice query transcription scheme for music information retrieval. The proposed scheme analyzes monophonic voice signal and generates its transcription for diverse music retrieval applications. For accurate transcription, we propose several advanced features including (i) Energetic Feature eXtractor (EFX) for onset, peak, and transient area detection; (ii) Modified Windowed Average Energy (MWAE) for defining multiple small but coherent windows with local threshold values as offset detector; and finally (iii) Circular Average Magnitude Difference Function (CAMDF) for accurate acquisition of fundamental frequency (F0) of each frame. In order to evaluate the performance of our proposed scheme, we implemented a prototype music transcription system called AMT2 (Automatic Music Transcriber version 2) and carried out various experiments. In the experiment, we used QBSH corpus [1], adapted in MIREX 2006 contest data set. Experimental result shows that our proposed scheme can improve the transcription performance.

• Bulletin of the Korean Chemical Society
• /
• v.29 no.7
• /
• pp.1335-1343
• /
• 2008

Theoretical studies on the un-catalyzed and catalyzed aminations of ketene with $NH_3$ and $(NH_3)_2$, respectively, were studied using MP2 and hybrid density functional theory of B3LYP at the 6-31+G(d,p) and 6- 311+G(3df,2p) basis sets in the gas phase and in benzene and acetonitrile solvents. In the gas phase reaction, the un-catalyzed mechanism was the same as those previously reported by others. The catalyzed mechanism, however, was more complicated than expected requiring three transition states for the complete description of the C=O addition pathways. In the un-catalyzed amination, rate determining step was the breakdown of enol amide but in the catalyzed reaction, it was changed to the formation of enol amide, which was contradictory to the previous findings. Starting from the gas-phase structures, all structures were re-optimized using the CPCM method in solvent medium. In a high dielectric medium, acetonitrile, a zwitterions formed from the reaction of $CH_2$=C=O with $(NH_3)_2$, I(d), exists as a genuine minimum but other zwitterions, I(m) in acetonitrile and I(d) in benzene become unstable when ZPE corrected energies are used. Structural and energetic changes induced by solvation were considered in detail. Lowering of the activation energy by introducing additional $NH_3$ molecule amounted to ca. −20 $\sim$ −25 kcal/mol, which made catalyzed reaction more facile than un-catalyzed one.