• Bulletin of the Korean Chemical Society
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• v.34 no.11
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• pp.3185-3186
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• 2013

• Bulletin of the Korean Chemical Society
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• v.32 no.spc8
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• pp.2877-2878
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• 2011

• Bulletin of the Korean Chemical Society
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• v.28 no.10
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• pp.1665-1669
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• 2007

A direct regioselective α-hydroxyamination of α-branched aldehydes with nitrosobenzene using cis-5-benzylproline as catalyst has been developed for the preparation of α-hydroxyamino aldehydes possessing a quaternary carbon center. Such compounds are versatile building blocks for the synthesis of quaternary α- amino acids, β-amino alcohols, and 1,2-diamines.

• Polymer(Korea)
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• v.30 no.3
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• pp.224-229
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• 2006

Quaternary ammonium salt terminated silane was prepared from aminopropyldimethylethoxysilane with methyliodide and ionized 7,7,8,8-tetracyanoquinodimethane $(Li^+TCNQ^-)$ was prepared from TCNQ with methyliodide and lithium iodide. Quaternary ammonium salt silane-TCNQ adduct (ST) was prepared by reacting quaternary ammonium salt terminated silane with $Li^+TCNQ^-$ solution. Poly (dimethylsiloxane)-ST adduct (PST) was prepared by condensation of $\alpha,\omega-hydroxyl$ group terminated poly (dimethylsiloxane) (PDMS) with ST. Maleated polyethylene modified with PDMS (PST-g-MPE) was prepared by melt polymerization of maleated PE and PST in internal mixer and PST-g-MPE/carbon black (CB) and MPE/CB composites were prepared by compounding PST with MPE and PST-g-MPE, respectively. The thermal and mechanical properties of the composites were measured and dispersion characteristics of CB in matrix rosins show that the dispersion of CB in PST-g-MPE/CB was better than that of MPE/CB composite.

• Polymer(Korea)
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• v.31 no.1
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• pp.80-85
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• 2007

Maleic anhydride (MA) modified ethylene-propylene-diene terpolymer (MEPDM) was pre-pared from solution polymerization. MEPDM-g-PST copolymer was prepared by melt polymerization of male ate d EPDM and quaternary ammonium silyl polydimethylsiloxane -7,7,8,8- tetracyanoquinodimethane (TCNQ) adduct (PST) in internal mixer and MEPDM-g-PST/HDPE/CB (MPEC) was prepared by com-pounding HDPE, MEPDM-g-PST copolymer and carbon black (CB, 5, 10, 15, and 20 phr), and HDPE/ CB (PEC) by compounding HDPE and CB (5, 10, 15, and 20 phr), respectively. The structure of MEPDM-g-PST copolymer was confirmed by measuring the FTIR. The maximum grafting ratio of MA onto EPDM was 2.35%. The thermal and mechanical properties of the composites were measured and dispersion characteristics of CB in matrix show that CB in MPEC was better dispersed than that in PEC composite.

• International Journal of Precision Engineering and Manufacturing
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• v.9 no.4
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• pp.63-65
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• 2008

The increased interest in reducing the environmental effects caused by releasing organic compounds and aqueous waste has motivated the development of polymeric materials in supercritical fluids. Recently, supercritical fluids have been used in material synthesis and processing because of their special properties, such as high diffusivity, low viscosity, and low surface tension. Supercritical carbon dioxide is the most attractive because it is non-toxic, non-flammable, and has moderate critical temperature and critical pressure values. Supercritical carbon dioxide can also swell most polymers. In this study, we prepared polymer/clay nanocomposites using supercritical fluids. Cloisites 10A, 15A, 25A, and 30B used in this study are montmorillonites modified with a quaternary ammonium salt. The nanocomposites of polymer/clay were characterized by X-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry.

• The Korean Journal of Quaternary Research
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• v.4 no.1
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• pp.27-40
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• 1990

$^{14}C$ age dating by AMS (accelerator mass spectrometry) technique was performed on twenty five small sized fossil shells and one peat taken from the sixteen piston cores in the southern and southeastern Korean Sea. AMS technique is available to date only a few milligram of amorphous carbons compare than conventional dating technique. It is described in detail of sample pre-treatment and experimental, and applied to the reconstruction of the sea level changes since the late Pleistocene in the Korean Sea. Dated age ranges from 520$\pm$100 to older than 33,500 years. Sedimentary facies in the study area represents a different environmental set which is affected by sea level fluctuation since the late Pleistocene.

• The Korean Journal of Quaternary Research
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• v.22 no.1
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• pp.28-36
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• 2008

The present study has focused on the environmental changes and evidences for sedimentation in the Lake Khuvsgul catchment during the Holocene period, inferred from short core sediment (BO03) from the eastern shore of Borsog Bay, which were analyzed in order to review records of the Holocene climatic evolution and Holocene history in Northern Mongolia. For the purpose of reconstruction of natural phenomenon that occurred in the lake catchment system during the Holocene, physical and chemical properties including HCl-soluble material, biogenic silica, organic matter and grain size distribution of minerals in the core sediments have been analyzed in this study. The vertical variations in composition for these properties show distinctly that five lines of paleoenvironmental evidence occurred in the lake catchment during the Holocene. A modified age model resulting from AMS carbon dating for the BO03 core sediment shows timings of these environmental events at 9.5 Kyr BP, 8.0 Kyr BP, 5.6 Kyr BP and 3.2 Kyr BP, respectively. Paleoenvironmental changes in the Lake Khuvsgul catchment system during the Holocene highlight distinctive features of the hydrological regime and geomorphologic evolution in the lake catchment due to regional landscape and global climatic changes corresponding with the Holocene optimum and thermal optimum. In particular, the change of hydrologic regime based on the sedimentological evidence has been caused by not only overland flow due to melting water, but also base flow due to thick permafrost around Khuvsgul region.

• Membrane Journal
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• v.32 no.5
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• pp.348-356
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• 2022

With the development of the bio industry, membrane chromatography with a high adsorption efficiency is emerging to replace the existing column chromatography used in the downstream processes of pharmaceuticals, food, etc. In this study, through the deacetylation reaction of two commercial cellulose acetate (CA) membranes with different pore sizes, the porous regenerated cellulose (RC) supports for membrane chromatography were obtained to attach the anion exchange ligands. The adsorptive membranes for anion exchange were prepared by attaching an anion exchange ligand ([3-(methacryloylamino) propyl] trimethylammonium chloride) containing quaternary ammonium groups on the RC supports by grafting and UV polymerization. The protein adsorption capacities of the prepared membranes were obtained through both the static binding capacity (SBC) and the dynamic adsorption capacity (DBC) measurement. As a result, the membrane chromatography with the smaller the pore size, the larger the surface area showed the highest protein adsorption capacity. Membrane chromatography which was prepared by using deacetylated commercial CA support with MAPTAC ligand (i.e., RC 0.8 + MAPTAC: 43.69 mg/ml, RC 3.0 + MAPTAC: 36.33 mg/ml) showed a higher adsorption capacity compared to commercial membrane chromatography (28.38 mg/ml).

• Proceedings of the Korean Vacuum Society Conference
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• 2011.08a
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• pp.198-198
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• 2011

Organocatalysis is a relatively new and popular area within the field of chiral molecule synthesis. It is one of the main branches of enantioselective synthesis with enzymatic and organometallic catalysis. In recent years, immense high quality studies on catalysis by chiral secondary amines were reported. These progresses instantly led to different organocatalytic activation concepts, so thousands of researchers from academia and the chemical industry are currently involved in this field and new ideas, new approaches, and creative thinking have been rapidly emerged. Organocatalysts, some of which are natural products, appear to solve the problems of metal catalysts. Compared to metal-based catalysis, they have many advantages including savings in cost, time, and energy, easier experimental procedure, and reduction of chemical waste. These benefits originate from the following factors. First, organocatalysts are generally stable in oxygen and water in the atmosphere, there is no need for special equipments or experimental techniques to operate under anhydrous or anaerobic conditions. Second, organic reagents are naturally available from biological materials as single enantiomers that they are easy and cheap to prepare which makes them suitable for small-scale to industrial-scale reactions. Third, in terms of safety related catalysis, small organic molecules are non-toxic and environmentally friendly. Therefore, the purpose of this research is to develop novel synthetic methods and design for various organocatalyst. Furthermore, it is expected that these organocatalysts can be applied to a variety of asymmetric reactions and study the transition state of these reactions using a metal sulface. Here, we report the synthesis of unprecedented organocatalysts, proline and pyrrolidine derivatives with quaternary carbon center.