• Journal of Microbiology and Biotechnology
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• 제19권9호
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• pp.946-950
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• 2009

In the course of screening for apoptotic substances that induce apoptosis in human leukemia U937 cells, a fungal strain, F000487, which exhibits potent inducible activity, was selected. The active compound was purified from an ethyl acetate extract of the microorganism by Sep-pak $C_{18}$ column chromatography and HPLC, and was identified as atromentin by spectroscopic methods. This compound induced caspase-3 processing in human leukemia U937 cells. The caspase-3 and poly (ADP-ribose) polymerase (PARP) were induced by atromentin in a dose-dependent manner. Furthermore, DNA fragmentation was also induced by this compound in a dose-dependent manner. These results show that atromentin potently induces apoptosis in U937 cells and that atromentin-induced apoptosis is related to the selective activation of caspases.

• 한국콘크리트학회:학술대회논문집
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• 한국콘크리트학회 2005년도 추계 학술발표회 제17권2호
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• pp.571-574
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• 2005

This study investigated the strength of concrete to improve construction material with polymer cement mortar. Some mixtures composed of Styrene-Butadiene Rubber(SBR) and Ethylene Vinyl Acetate(EVA) Poly Vinyl Alcohol(PVA) were studied. The three mixtures carried out the physical, mechanical test to determine its properties which a include : compressive, flexural, bond strength test. The test results show that the compressive strength was increased at long-term age when compared to early ages for increasing polymer contents. It was found that flexural strength and bond strength became larger as polymer to cement ratio became higher.

• 한국전기전자재료학회논문지
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• 제30권7호
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• pp.413-416
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• 2017

We investigated solution-processed indium-yttrium-oxide (IYO) TFTs using apoly (methyl methacrylate) (PMMA) passivation layer. The IYO semiconductor solution was prepared with 0.1 M indium nitrate hydrate and 0.1 M yttrium acetate dehydrate as precursor solutions. The solution-processed IYO TFTs showed good performance: field-effect mobility of $13.13cm^2/Vs$, a threshold voltage of 8.2 V, a subthreshold slope of 0.93 V/dec, and a current on-to-off ratio of $7.2{\times}10^6$. Moreover, the PMMA passivation layers used to protectthe IYO active layer of the TFTs, did so without deteriorating their performance under ambient conditions; their operational stability and electrical properties also improved by decreasing leakage current.

• 한국콘크리트학회:학술대회논문집
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• 한국콘크리트학회 1998년도 봄 학술발표회 논문집(I)
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• pp.231-236
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• 1998

In general, the drying shrinkage of polymer-modified mortars using redispersible polymer powders is much higher than that of unmodified mortar. The purpose of this study is to reduce the drying shringkage of polymer-modified mortars using a redispersible poly(ethylene-vinyl acetate) (EVA) powder, which is widely used for the manufacture of prepackaged-type polymer-modified mortar products at present. Polymer-modified mortars using the redispersible EVA powder with powdered shrinkage-reducing agent were prepared with various polymer-cement ratios and shrinkage-reducing agent contents, and tested for drying shrinkage and strength. From the test results, the drying shrinkage of the redispersible EVA powder-modified mortars with a powdered shrinkage agent is remarkably reduced with increasing shrinkage-reducing agent content, and becomes approximately a half of that of the redispersible EVA powder-modified mortars with the same polymer-cement ratios and without the shrinkage-reducing agent at a shrinkage-reducing agent content of 6%.

• Macromolecular Research
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• 제16권7호
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• pp.620-625
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• 2008

A novel nitrogen-phosphorus compound, diphenyl piperazine-1,4-diylbis(methylphosphinate)(DPPMP) was synthesized via a two step reaction and its flame retarding efficiency as a single component additive was investigated. The success of synthesis was confirmed by FTIR and $^1H$ and $^{31}P$ NMR analysis. The product was mixed with polycarbonate (PC), poly(butylene terephtalate) (PBT), ethylene-vinyl-acetate copolymer (EVA), and acrylonitrile-butadiene-styrene copolymer (ABS). The flame-retarding efficiency was evaluated using the limiting oxygen index (LOI) and the UL-94 vertical test methods. The addition of DPPMP enhanced the flame retardancy of the polymers and the V-0 ratings were obtained for the polymers examined in this study at a loading of 7-30 wt%. The gas-phase flame retardancy mode of action was suggested for this material from the thermogrametry experiment results.

• ETRI Journal
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• 제31권6호
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• pp.636-641
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• 2009

ZnO nanofibers were electro-spun from a solution containing poly 4-vinyl phenol and Zn acetate dihydrate. The calcination process of the ZnO/PVP composite nanofibers brought forth a random network of polycrystalline wurtzite ZnO nanofibers of 30 nm to 70 nm in diameter. The electrical properties of the ZnO nanofibers were governed by the grain boundaries. To investigate possible applications of the ZnO nanofibers, their CO and $NO_2$ gas sensing responses are demonstrated. In particular, the $SnO_2$-deposited ZnO nanofibers exhibit a remarkable gas sensing response to $NO_2$ gas as low as 400 ppb. Oxide nanofibers emerge as a new proposition for oxide-based gas sensors.

• Carbon letters
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• 제23권
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• pp.55-62
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• 2017

We report on the dispersion state of partially reduced graphene oxide (PRGO) in organic solvents, namely methyl ethyl ketone, ethyl acetate, methylene chloride, toluene, and xylene, by controlling the carbon to oxygen (C/O) atomic ratio of the PRGOs. A two-phase solvent exchange method is also proposed to transfer PRGO from water to an aprotic solvent, such as methyl ethyl ketone. We achieve relatively good dispersion in aprotic and non-polar solvents by controlling the C/O atomic ratio of the PRGOs and applying the two-phase solvent exchange method. There is an increase in the glass transition temperatures with the dispersion of PRGOs into amorphous polymers, in particular a $4.4^{\circ}C$ increase for poly(methyl methacrylate) and $3.0^{\circ}C$ increase for polycarbonate. Good dispersion of PRGO in a nonpolar polymer, such as linear low density polyethylene, is also obtained.

• Elastomers and Composites
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• 제55권1호
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• pp.6-12
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• 2020

Poly(ethylene-co-vinyl acetate) compounds and vulcanizates containing dicumyl peroxide (DCP) (HD) were prepared, and the curing agent and reaction products were analyzed using gas chromatography/mass spectrometry (GC/MS). Samples containing trially cyanurate (TAC) and DCP (HDT) were also prepared and analyzed. Some raw DCP were decomposed in the injector region of GC to produce acetophenone. DCP was detected in the HD compound but was not observed in the HD vulcanizate, and instead acetophenone and 2-phenyl-2-propanol were detected. Both DCP and TAC were observed in the HDT compound but not in the HDT vulcanizate, where acetophenone and 2-phenyl-2-propanol were detected. Thus, some of the DCP decomposed during the compounding process. The formation mechanism for acetophenone and 2-phenyl-2-propanol during the crosslinking reaction was identified, and differences in the crosslinking reactions of HD and HDT compounds were discussed.

• 방사선산업학회지
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• 제3권1호
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• pp.31-37
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• 2009

This paper describes the preparation of manufacturing a new nanocomposite material, which involves adding a multi walled carbon nanotube (MWCNT) to improve thermal characteristics of poly (ethylene-co-vinyl acetate) (EVA). We irradiated the prepared nanocomposites with doses of 50 kGy, 100 kGy and 200 kGy at a dose rate of $5kGy\;hr^{-1}$ and examined their thermal stability, activation energy and crosslink level by using a thermogravimetric analyzer (TGA) and gel fraction experiments. TGA results indicated that the samples with a MWCNT had higher Derivative Thermo Gravimetry (DTG) 2nd peak temperatures than those without a MWCNT. And activation energy of the samples reduced as the absorption dose and the MWCNT content increased. Finally, the gel fraction increased rapidly up to 100 kGy as total absorption dose increased, and then the growth rate of all samples was slowly increased from 100 kGy.

• Bulletin of the Korean Chemical Society
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• 제16권11호
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• pp.1099-1104
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• 1995

The catalyzed polycondensations of bis(2-hydroxyethyl) naphthalate were kinetically investigated in the presence of various antimony compounds as a catalyst. The polymerization were investigated with various ligand types of antimony oxides, various concentrations of antimony triacetate and titanium/antimony mixed catalysts. The time to reach the maximum molecular weight was remarkably changed in each case. With increasing the concentration of antimony acetate, the propagation rate was largely increased, while the degradation rate was slightly decreased. It also can be seen that the propagation and degradation rate were larger influenced by the equimolecular titanium/antimony mixed catalyst than other mixed catalysts. The temperature dependence of bis(2-hydroxyethyl) naphthalate with antimony triacetate also has been studied. From the results, it was found that the propagation rate was less influenced by a temperature change than the degradation rate.