In this paper, a logger of an earthquake accelerometer in order to link and share the seismic data easily with related institutes is presented. The firmware is embedded into the logger, which transforms the seismic data into the formats, miniSEED.

An accelerometer that has optical fibers to measure the inclination and acceleration of the architectural structures was examined. This was to ensure precise measurement through the unification of the deformation rate sensor and the angular displacement sensor.

The purpose of this study was to evaluate the seismic performance of high-performance steel. For this study, the hysteretic behavior and deformation shape of steel beam-to-column connections with SM570TMC was investigated using non-linear finite element analysis. The non-linear finite element analysis was carried out using ANSYS. The displacement analysis of steel beam-to-column connections was conducted according to the qualifying procedures of current korean building code(KBC2009).

The antioxidative activity of various enzymatic extracts from Sarcodon aspratus (S. aspratus) was evaluated by measuring 1,1-diphenyl-2-picrylhydrazyl (DPPH), and alkyl radical scavenging activity using an electron spin resonance (ESR) spectrometer. For this study, the S. aspratus were enzymatically hydrolyzed by seven carbohydrases (Viscozyme, Celluclast, Dextrozyme, AMG, Promozyme, Maltogenase, and Termamyl) and eight proteases (α-chymotrypsin, Alcalase, Flavourzyme, Neutrase, papain, pepsin, Protamax, and trypsin). The DPPH radical scavenging activities of Viscozyme and pepsin extracts were the highest, and the half maximal inhibitory concentration (IC50) values were 0.896 and 0.734mg/mL, respectively. The Celluclast and trypsin extracts showed the highest scavenging activities on alkyl radical, and their IC50 values were 0.278 and 0.575mg/mL, respectively. The Celluclast extracts was decreased cell apoptosis in PC-12 cells against H2O2-induced oxidative damage. The findings of the present study suggest that enzymatic extracts of S. aspratus exhibit antioxidative activity against oxidative stress on PC-12 cells.