• Korean Chemical Engineering Research
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• v.46 no.5
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• pp.958-964
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• 2008

In this work, micro-sized dextran particles, which have recently been focused as one of the candidate materials for the Drug Delivery System(DDS), were prepared by means of the Supercritical Antisolvent (SAS) process with $CO_2$. With dimethyl sulfoxide(DMSO) as the solvent, effects of the operating variables such as temperature (308.15~323.15 K), pressure(90~130 bar), solute concentration(10~20 mg/ml), and the molecular weight of the solute(Mw=37,500, 450,000) on the size and morphology of the resulting particles were thoroughly observed. The higher solute concentration led to the larger particles, however, the injection velocity of the solution and pressure did not show significant effects on the resulting particle size. With dextran of the lower molecular weight, the smallest particles were obtained at 313.15 K. On the other hand, the size of the particles from the high molecular weight dextran ranged between $0.1{\sim}0.5{\mu}m$ with an incremental effect of the temperature and pressure. For the solute concentration of 5 mg/ml, the lower molecular weight dextran did not form discrete particles while aggregation of the particles appeared when the solute concentration exceeded 15 mg/ml for the higher molecular weight dextran. It is believed that if the solute concentration is too low, the degree of the supersaturation in the recrystallization chamber would not be sufficient for initiation of the nucleation and growth mechanism. Instead, the spinodal decomposition mechanism leads to formation of the island-like phase separation which appears similar to aggregation of the discrete particles. This effect would be more pronounced for the smaller molecular weight polymer system due to the narrower phase-splitting region.

• International Journal of Industrial Entomology and Biomaterials
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• v.5 no.2
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• pp.163-170
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• 2002

In this paper, silk fibroin (SF)/polyurethane (PU) blend films were fabricated to develop a new biomaterial for biomedical applications. These blend films were prepared using formic acid as a cosolvent, and structural characteristics and properties of blend films were investigated. FTIR results suggested that there was no specific interaction between SF and PU, implying molecular immiscibility in SF/PU blend films. Furthermore, it was revealed by XRD method that the crystalline region of blend components was not perturbed by counterpart polymers. The degree of phase separation of SF/PU blend films was diminished by increasing PU content in blend. Especially, the blend with 70% content of PU showed no evidence of macro-phase separation in SEM observation. However, SF/PU blend (70/30) was revealed to be phase-separated in a lower dimension confirmed by DMTA measurement. TGA result showed that thermal decomposition temperature of blend film was slightly decreased compared to those of SF and PU polymer itself, Though mechanical properties of SF/PU blend films were not good enough due to the solvent, blood compatibility of PU can be enhanced markedly by mixing with SF for SF/PU blend film.

• Korean Journal of Materials Research
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• v.24 no.10
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• pp.509-514
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• 2014

We demonstrate a simple and effective method to accurately position silicon nanowires (Si NWs) at desirable locations using drop-casting of Si NW inks; this process is suitable for applications in nanoelectronics or nanophotonics. Si NWs were assembled into a lithographically patterned sacrificial photoresist (PR) template by means of capillary interactions at the solution interface. In this process, we varied the type of solvent of the SiNW-containing solution to investigate different assembly behaviors of Si NWs in different solvents. It was found that the assembly of Si NWs was strongly dependent on the surface energy of the solvents, which leads to different evaporation modes of the Si NW solution. After Si NW assembly, the PR template was cleanly removed by thermal decomposition or chemical dissolution and the Si NWs were transferred onto the underlying substrate, preserving its position without any damage. This method enables the precise control necessary to produce highly integrated NW assemblies on all length scales since assembly template is easily fabricated with top-down lithography and removed in a simple process after bottom-up drop-casting of NWs.

• Proceedings of the Membrane Society of Korea Conference
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• 1996.04a
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• pp.16-19
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• 1996

Separation with synthetic membrane have become increasingly important processes in many fields. In the most application of membrane process, polymer membrane is used. the main advantage of polymers as a material for membrane preparation is the relative simplicity of this film formation which enables one to obtain rather high permeability rates. However, polymeric membranes have several limitations, such as high temperature instability, swelling and decomposition in organic solvent, et. al.. These limitations can be overcome by inorganic membrane. At the present time, commercially available inorganic membranes have pore diameters ranging 5nm to 50mm, and the predominant flow regime in such membrane is Knudsen diffusion. Since the Knudsen permeability is directly proportional to the molecular velocity, gases can be separated due to their molecular masses. However, this separation mechanism is only of important for light gases such as H2 and He. Other separation mechanisms like surface diffusion, active diffusion can play an important role only with very small pore diameters(2nm) and give rise to large permselectivities. Therefore, preparation of inorganic membrane with nano-sized pore have been attracting more and more attention.

• Bulletin of the Korean Chemical Society
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• v.35 no.5
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• pp.1385-1390
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• 2014

Hydrofluoroethers (HFEs) are developed as a suitable for the replacement of environmentally hazardous CFCs and are termed as third generation refrigerants. One of the major products of decomposition of HFEs in the atmosphere is a fluoroester. The present study relates to the OH and Cl initiated oxidation of $CF_3C(O)OCH_2CF_3$ formed from the oxidation of HFE-356mff. The latter is used as a solvent in the industry and reaches the atmosphere without any degradation. Kinetics of the titled molecule has been studied at MPWB1K/6-31+G(d,p) level of theory. Single point energy calculations have been made at G2(MP2) level of theory and barrier heights are determined. The rate constants are calculated using canonical transition state theory. Tunnelling correction are made using one-dimensional Eckart potential barrier. The rate constant calculated during the present study are compared with the experimental values determined using relative rate method and FTIR detection technique.

• Proceedings of the Korean Vacuum Society Conference
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• 2016.02a
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• pp.420.2-420.2
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• 2016

Various fields have been paid attention to upconversion nanoparticles (UCNPs) because of its unique optical properties. Moreover, to use the UC luminescent techniques through cell images for identified apoptosis/necrosis of cancer cells have been performed. They have been studied for a versatile biomedical application such as a biosensing tool, or delivery of active forms of medicines inside living cells. UCNPs have distinctive characteristics such as photoluminescence, special emission, low background fluorescence signal and good colloidal stability, which have many advantages compared with the organic dyes and quantum dots. UCNPs have not only a great potential for imaging (UC luminescence) but also therapies (photo-thermal therapy, PTT and photo-dynamic therapy, PDT) in cancer diagnostics. Therefore, we report the enhancement of upconversion red emission in NaYF4:Yb3+,Er3+ nanoparticles, synthesized via solid-state method with the thermal decomposition of trifluoroacetate as precursors and organic solvent at a high boiling point. The UCNPs have an emission in the field of near infrared wavelength, cubic shape and nano-size in length. In this study, we will further investigate it for cancer therapy with NIR optical detection onto the solid substrate.

• Korean Journal of Materials Research
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• v.21 no.3
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• pp.156-160
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• 2011

FePt nanoparticles suspension was synthesized by reduction of platinum acetylacetonate and decomposition of iron pentacarbonyl in the presence of oleic acid and oleyl amine. FePt nanoparticles were coated on a substrate by convective assembly from the suspension. To prevent the coalescence during the annealing of FePt nanoparticles double convective coatings were tried. First convective coating was for silica particle assembly on a silicon substrate and second one was for FePt nanoparticles on the previously coated silica layers. It was observed by scanning electron microscopy (SEM) that FePt nanoparticles were dispersed on the silica particle surface. After annealing at $700^{\circ}C$ for 30 minutes under nitrogen atmosphere, FePt nanoparticles on silica particles were maintained in a dispersed state with slight increase of particle size. On the contrary, FePt nanoparticles that were directly coated on silicon substrate showed severe particle growth after annealing due to the close-packing of nanoparticles during assembly. The size variation during annealing was also verified by X-ray diffractometer (XRD). It was suggested that pre-coating, which offered solvent flux oppose to the capillary force between FePt nanoparticles, was an effective method to prevent coalescence of nano-sized particles under high temperature annealing.

• Journal of the Korean Ceramic Society
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• v.45 no.3
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• pp.150-156
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• 2008

Pitch-binded activated carbon fiber(ACF)/$TiO_2$ composite photocatalysts were prepared by Carbon Tetra Chloride (CTC) solvent mixing method with different mixing ratios of anatase to ACF. The result of the textural surface properties demonstrated that there is a slight increase in the Brunauer, Emmett and Teller (BET) surface area of composites with an increase of the amount of ACF. The surfaces structure morphologies of the composites were observed using an Scanning Electron Microscope (SEM). In the XRD patterns for all ACF/$TiO_2$ composites, the diffraction peaks showed the formation of anatase crystallites. The EDX spectra showed the presence of C, O and Si with strong Ti peaks. Most of these samples were richer in carbon and major Ti metal than any other elements. From the photo-decomposition results, the excellent activity of the ACF/$TiO_2$ composites between c/$c_0$ for methylene blue and UV irradiation time could be attributed to both the effects of the photocatalysis of the supported $TiO_2$ and adsorptivity of activated carbon fiber and another carbon derived from pitch.

• Journal of environmental and Sanitary engineering
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• v.13 no.3
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• pp.102-112
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• 1998

The fate of polynuclear aromatic hydrocarbons(PAMs) in soil has drawn increasing concern due to their toxic, carcinogenic, and mutagenic effects. These compounds have been most commonly carried into the soil in solvent, as in a coal tar or cresote. This study has been focused on the applicability of microwave treatment of soils contaminated by PAHs. Studies have been conducted with soil(particle diameter $150~500{\mu}m$), which was spiked with naphthalene, acenaphthene, fluorene, anthracene and pyrene, with different moisture contents. According to the results of the research, up to 95% removal efficiency of naphthalene was observed in 10% moisturized soil for five minutes microwave inducing And the removal efficiency of acenaphthene and fluorene were observed to be 88.9%, 67.2% in 30% moisturized soil, respectively. Due to the low vapor pressure, anthracene and pyrene showed the low removal efficiency. In case the powdered activated carbon was added to the soil as a sensitizer, anthracene and pyrene were decomposed into a various by-products. Decomposition rates of anthracene and pyrene were increased with incresing addition of a PAC to the soil. It is concluded that the developement of a microwave process to remediate soils contaminated with PAHs is foreseeable. But additional studies are also needed regarding continuous microwave heating process.

• Applied Chemistry for Engineering
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• v.5 no.4
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• pp.657-661
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• 1994

A method to analyse the concentration of mixture (AC/urea) and the concentration of urea or AC alone was developed. In this study, the decomposition of AC solution to ammonium bicarbonate was suppressed by using of 15% w/v ammonia as a solvent and the error of equilibrium point was maintained less than 1 %. Strong peaks at $1600cm^{-1}$ for urea and at $1405cm^{-1}$ for AC, corresponding to the N-H bending and symmetric carboxylate ion stretch were used to construct calibration graph and equations for the measurement of concentration. The errors of calculated concentration were ${\pm}0.1%$ w/v for AC and ${\pm}0.3%$ w/v for urea.