• Textile Coloration and Finishing
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• v.17 no.1
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• pp.45-51
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• 2005

Soluble keratose(S-keratose) could be obtained by oxidizing the wool keratin with performic acid. S-keratose/PVA solutions were made by dissolving them in the formic acid and S-keratose/PVA web of sub-micron size was made by electro-spinning technique. SEM, elemental analysis, FT-IR, X-ray diffractometry, and TGA were used to characterize the properties of S-keratose/PVA solutions and fibers. As the S-keratose content in S-keratose/PVA solution increased, viscosity of solution decreased while electrical conductivity has increased. The fiber diameter has decreased with increasing the S-keratose content. S-keratose/PVA ratio in fibers were similar to the ratio in the solutions. The crystalline structures of S-keratose and PVA existed separately in the electrospun webs. Thermal stability of the web increased with the PVA content increasing.

• Journal of the Korean Graphic Arts Communication Society
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• v.22 no.2
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• pp.111-122
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• 2004

The purpose of this study was to investigate the possibility of application of microwave energy for the fabrication of polymer/clay nanocomposite. APES/Clay nanocomposites were prepared at $130^{\circ}C$ for 30min with various amount of MMT or OMMT used the melt-intercalation method applied the classical and microwave heating source. APES/Clay samples were characterized by the means of X-ray diffractometry (XRD), transmitted electron microscopy (TEM) differential scanning calorimetry (DSC), and rheometric dynamic analysis (RDA). It was found that intercalated or exfoliated state of the samples could be controlled by the clay type, clay content, and heating type.

• Journal of Pharmaceutical Investigation
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• v.18 no.3
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• pp.99-105
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• 1988

Inclusion complex formation of furosemide with ${\beta}-cyclodextrin({\beta}-CyD)$ in solid state was confirmed by X-ray diffractometry, IR spectroscopy and differential scanning calorimetry (DSC). The solid complexes of ${\beta}-CyD$ with furosemide in molar ratio of 2 : 1 were prepared by solvent evaporation method. The photodegradation of furosemide in alkaline solution under the light and the hydrolysis of furosemide in acidic solution were not inhibited by complex formation with ${\beta}-CyD$. However, the bioavailability of furosemide was improved by complex formation with ${\beta}-CyD$ after oral administration to rats.

• Journal of Environmental Science International
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• v.13 no.4
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• pp.429-434
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• 2004

The purpose of this study was to investigate the possibility of application of microwave energy for the fabrication of polymer/clay nanocomposite. APES/Clay nanocomposites were prepared at 13$0^{\circ}C$ for 30min with various content of clay by melt-intercalation method under classical and microwave heating source. APES/Clay samples were characterized by the means of X-ray diffractometry(XRD), thermal gravimetric analysis(TGA), and rheometric dynamic analysis(RDA). It was found that intercalated or exfoliated state was obtained in the samples according to the condition of organic modification, clay content, and heating source.

• 한국정보디스플레이학회:학술대회논문집
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• 2008.10a
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• pp.330-332
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• 2008

Banana-shaped molecules were synthesized introducing ester linking group into mesogenic unit, varying the central unit with 1,6-, 2,3-naphthylenes, and introducing the hexyloxy group as the terminal flexible unit. The properties of the compounds were characterized by FT-IR, NMR spectroscopy, DSC, polarizing optical microscopy, and X-ray diffractometry.

• Journal of the Korean Ceramic Society
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• v.27 no.3
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• pp.383-388
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• 1990

Hydraulic properties of CA2-based clinker synthesized by Hydration-Burning Method was studied by calorimetry, analysis of suspension, thermogravimetry, scanning electron microscopy and X-ray diffractometry. Hydraulic properties of the clinker was so activated that heat of hydration of the clinker evolved faster than that of CA synthesized by conventional method. In suspension of W/C=33, dissolution of the clinker began at nearly same time as that of CA, but precipitation of AH3 and rise of [OH-] occurred fairly faster in the suspension of the clinker than that of CA. From the beginning of hydration, AH3 was produced and became a main phase of the hydrate with minor phase of CAH10 and C2AH8, but C3AH6 was not produced at ambient temperature.

• Structural Engineering and Mechanics
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• v.31 no.1
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• pp.1-10
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• 2009

An experimental investigation was conducted to evaluate the performance of mortars with and without Metakaolin (MK) exposed to elevated temperatures $200^{\circ}C$, $400^{\circ}C$, $600^{\circ}C$ and $800^{\circ}C$ for two hours. The binder to sand ratio was kept constant (1:5.23). The ordinary Portland cement (OPC) was replaced with MK at 0%, 5%, 10% 20% and 30%. All mixtures were designed to have a flow of $94{\pm}5%$. The compressive strength of mortars before and after exposure to elevated temperature was determined. The formation of various decomposition phases were identified using X-ray diffractometry (XRD) and differential thermal analysis (DTA). The microstructure of the mortars was examined using scanning electron microscope (SEM). Test results indicated that MK improves the compressive strength before and after exposure to elevated temperature and that the 20% cement replacement of MK is the optimum percentage.

• Bulletin of the Korean Chemical Society
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• v.23 no.9
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• pp.1201-1210
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• 2002

A new series of hyperbranched aromatic polyesters containing azoxybenzene mesogens and polymethylene spacers were prepared by polymerizing AB2 type monomers that have the isophthaloyl dicarboxylic acid terminal at one end and the p-oxyp henol terminal at the other end. The monomers contain a built-in azoxybenzene mesogen that is linked to the terminal groups through polymethylene spacers. The polyesters prepared were characterized by solution viscosity, differential scanning calorimetry, X-ray diffractometry and polarizing microscopy. All of the polyesters were found to be thermotropic (nematic). Their glass-transition temperatures and mesophase temperature ranges were very sensitive to the length of the two spacers existing in the repeating unit. The degree of branching of one of the polyesters was determined by the NMR spectroscopy and found to be 0.56.

• Journal of Magnetics
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• v.9 no.2
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• pp.65-68
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• 2004

Magnetically soft nanomaterials obtained by controlled crystallisation of metallic glasses are the newest group of materials for inductive components. In particular, research is carried out in the field of alloys for high temperature applications. This kind of materials must meet two basic requirements: good magnetic properties and stability of properties and structure. In the present work the magnetic properties and structure of Fe-Co-Hf-Zr-Cu-B (HIDTPERM-type) alloys were investigated, as well as their stability. Differential thermal analysis, (DTA), X-ray diffractometry (XRD), transmission electron microscopy (TEM), magnetometry (VSM) and quasistatic hysteresis loop recording were used to characterise structure and properties of the alloys investigated. Optimisation against properties and their stability was performed, resulting in formulation of chemical composition of the optimum alloy, as well as its heat treatment.

• Elastomers and Composites
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• v.52 no.2
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• pp.131-135
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• 2017

Zinc nitrate hexahydrate [$Zn(NO_3){\cdot}6H_2O$] and sodium hydroxide [NaOH] were used as source reagents in the preparation of ZnO nanoparticles in an aqueous solution containing deionized water and ethanol in a ratio of 2:5 (v/v). ZnO nanoparticles were heated in an electric furnace at $700^{\circ}C$ for 2 h under an atmosphere of inert argon gas. The morphological and structural properties of the nanoparticles were characterized by scanning electron microscopy (SEM) and powder X-ray diffractometry (XRD). UV-vis spectrophotometry was used to analyze the photocatalytic degradation of 3-nitrophenol with ZnO nanoparticles as photocatalyst under ultraviolet irradiation at 254 nm. Evaluation of the kinetic of the photo-catalytic degradation of 3-nitrophenol indicated that the degradation of 3-nitrophenol with ZnO nanoparticles obeyed the pseudo-first order reaction rate model.