• Polymer Science and Technology
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• v.2 no.3
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• pp.158-168
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• 1991

본고에서는 고분자절연체의 내부전하분포 측정을 위한 측정원리, 측정장치 및 실제측정예 등에 대하여 언급하였다. 이 방법은 고분자내에 존재하는 전하의 종류, 위치 및 전하량에 대한 정보를 얻을 수 있으므로 고분자의 절연성질을 이해하는데 도움을 줄 것으로 생각한다. 특히 폴리에틸렌의 경우 여러 가지 요인, 즉 수지의 종류 또는 첨가제의 유무 등에 의해 각기 다른 내부전하분포를 갖는다는 사실이 밝혀졌다. 이와 같은 사실은 고분자 내부에 존재하는 공간 전하 때문에 외부전압에 의한 전기장이 변형되고 이에 따라 고분자의 절연성질이 변형될 수 있다는 점을 생각할 때 매우 중요한 의미를 갖는다고 할 수 있다. 따라서 고분자의 절연성질에 대한 이해를 높이기 위하여는 절연성질과 내부전하분포와의 관계에 대한 보다 깊은 연구가 이루어져야 할 것으로 생각된다.

• Applied Biological Chemistry
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• v.43 no.4
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• pp.241-246
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• 2000

In order to investigate structural properties of Chindo black rice(grown in Chindo, Chonnam) starch and its amylopectin, Chindo black rice was investigated in comparison to Shinsun waxy rice. The maximum absorbance wave and intrinsic viscosity of Chindo black rice starch and Shinsun waxy rice starch were 523 nm, 521 nm and 183 ml/g, 178 ml/g, respectively. ${\beta}-amylolysis$ limit(%) of Chindo black rice and Shinsun waxy rice starch were 62.8% and 60.3%, respectively. Chindo black rice was determined to be a waxy rice due to the results of iodine reaction and elution profile on Sephroce CL-2B. The chain of amylopectins in Chindo black rice distributed fraction 1$(F_1)$ of above degree of polymerization$({\overline{DP}})$ 55, fraction 2$(F_2)$ of ${\overline{DP}} $40{\sim}50$ and fraction 3$(F_3)$ of ${\overline{DP}} $15{\sim}20$, and the ratio of $F_3$ to $F_2$ for Chindo black rice was higher than that for Shinsun waxy rice. The super long chain of amylopectin in Chindo black rice was consisted much more than that of Shinsun waxy rice. ${\beta}-limit$ dextrins in Chindo black rice amylopectin distributed $F_1$ of above ${\overline{DP}} 55, $F_2$ of ${\overline{DP}} $30{\sim}45$ and $F_3$ of ${\overline{DP}} $10{\sim}20$. Little difference was shown between elution patterns of the pullulanase treated ${\beta}-limit$ dextrins of Chindo black rice amylopectin and Shinsun waxy rice amylopectin. These results suggest that Chindo black rice starch was similar to Shinsun waxy rice starch.

• Korean Chemical Engineering Research
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• v.43 no.6
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• pp.704-714
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• 2005

Phase separations of Poly(4-vinylphenol)(PVPh)/Ethyl Acetate and PVPh/Butyl Acetate solutions were measured using the thermal optical analysis (TOA) method. The experimental phase separation data were correlated with liquid-liquid equilibria relations based on PC-SAFT equation of state. The phase separations of these system showed the behaviors of LCST (lower critical solution temperature)-type. The measured cloud temperatures were lowered with increasing in molecular weights of polymer(PVPh), and cloud temperatures of PVPh/Ethyl Acetate solutions shifted to lower temperature regions, compared to the PVPh/Butyl Acetate solutions. Extents of cross-association between solvent molecule and polymer in the PVPh/Ethyl Acetate solutions were measured using the FT-IR spectrum analysis method, and cross-association parameters of PC-SAFT model were estimated from experimental extents of cross-association. By using the estimated cross-association parameters between PVPh and solvent molecule, binodal and spinodal curves of liquid-liquid equilibria in PVPh/Ethyl Acetate and PVPh/Butyl Acetate solutions were calculated from PC-SAFT equation of state. The calculated binodal curves of these system were shown to be well agreeable with the experimental cloud temperature curves.

• Proceedings of the Korea Technical Association of the Pulp and Paper Industry Conference
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• 2010.04a
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• pp.193-193
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• 2010

이전의 연구에서 우리는 선응집 기술을 적용한 중질탄산칼슘의 크기에 따른 수초지의 물성을 평가하였다. 이때 선응집 기술이 적용된 충전물의 입도와 분포를 측정하기 위해 light diffraction spectroscopy (LDS) 가 사용되었다. 경질탄산칼슘과 양이온성 고분자의 흡착 현상을 알아보기 위한 이번 연구에도 LDS가 사용되었으며, 일회성으로 입자의 크기와 분포를 측정하는 것에서 더 나아가 시간의 흐름에 따라 응집체의 형성과 파괴, 재성장을 관찰할 수 있는 도구로서 역할 하였다. 본 연구에서 우리는 세 가지 경우로 나누어 경질탄산칼슘의 응집 현상을 관찰하였다. 첫째로 경질탄산칼슘에 흡착되는 양이온성 고분자의 특성, 분자량과 전하밀도, 을 달리하여 응집체의 성장과 파괴를 관찰하였다. 둘째, 양이온성 고분자로 중질탄산칼슘을 응집시켜, 경질탄산칼슘 응집체의 경우와 입도와 전단 안정성 등을 비교하였다. 마지막으로 나노 크기의 실리카 투입이, 마이크로 크기의 경질탄산칼슘 응집체가 강한 전단에 의해 파괴되었을 때, 응집체의 전단 안정성이나 재성장 측면에 도움을 주는지 관찰하였다. 내첨용 충전물로써 경질탄산칼슘의 사용이 전 세계적으로 늘고 있는 시점에서 양이온성 고분자 첨가에 의한 경질탄산칼슘의 응집 현상을 관찰하는 것은 일반적인 제지 공정에서 경질탄산칼슘의 거동을 이해하는데 도움이 될 뿐만 아니라, 내첨용 충전물 첨가에 따른 종이의 강도 저하 방지를 위한 선응집 기술의 적용에도 도움이 될 수 있을 것으로 생각한다.

• Applied Chemistry for Engineering
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• v.8 no.5
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• pp.844-852
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• 1997

In the polymerization of ethylene to produce crystalline polyethylene wax using the homogeneous titanium-based catalyst, the effects of various parameters such as catalyst, temperature, pressure, comonomer and time on the performance of catalyst and the properties of polyethylene wax were investigated. The properties of polyethylene wax obtained were characterized in terms of molecular weight, molecular weight distribution, crystallinity, density and morphology. Among the polymerization features with a series of mixed cocatalyst systems of $(C_2H_5)_3Al$, $(i-C_4H_9)_3Al$, $(C_2H_5)_2AlCl$ and $(C_2H_5)_3Al_2Cl_3$, it turned out that the combination of $(C_2H_5)_3Al$ and $(C_2H_5)_3Al_2Cl_3$ was more effective than any other combination. It was noted that the activity of catalyst and the properties of polyethylene wax were affected by the polymerization parameters, i.e. time, temperature and hydrogen partial pressure. The various kinds of crystalline polyethylene wax could be obtained by careful control of these parameters. Also we could obtain low density polyethylene wax which has density down to 0.91 g/cc by use of 1-butene as a comonomer.

• 한국생물공학회:학술대회논문집
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• 2003.04a
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• pp.334-338
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• 2003

In this study, We evaluated the removal efficiency of natural organic matters(NOM) in the Ultrafiltration(UF) and Nanofiltration(NF) membranes with molecular weight cutoff of 2500(GH), 8000(GM) and 250(HL), respectively. Filtration type was cross-flow filtration. The investigation result about raw water structure was hydrophobic 28%, hydrophilic 53% and transphilic 19%, in conjunction with XAD8/4 resin fractionation method. We were compared with UF(GM, GH) and NF(HL), in operation characteristic. In spite of poor MWCO, GM(8000Da) was superior than GH(2500Da), in the efficiency of total operation. It was showed the NF(HL) 80%, UF(GM) 50%, in the removing efficiency of HAAFP.

• Journal of Korean Society of Water and Wastewater
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• v.22 no.1
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• pp.31-38
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• 2008

The primary objective of this study was to evaluate the variation of the molecular size distribution by granular activated carbon (GAC) adsorption. GAC adsorption was assessed by using the rapid small-scale column test (RSSCT) and high-performance size-exclusion chromatography (HPSEC) was used to analyze the molecular size distribution (MSD) in the effluent of GAC column. RSSCT study suggested that GAC adsorption exhibited excellent interrelationship between dissolved organic carbon (DOC) breakthrough and MSD as function of bed volumes passed. After GAC treatment, the nonadsorbable fraction which was about 25percents of influent DOC corresponded to the hydrophilic (HPI) natural organic carbon (NOM) of NOM fractions and was composed entirely of <300 molecular weight (MW) in the HPSEC at the initial stage of the RSSCT operation. The dominant MW fraction in the source water was 1,000~5,000daltons. At the bed volumes 2,500, MW <500 of GAC treated water was risen rather than it of source water. After the bed volumes 7,300 of operation, the MW 1,000~3,000 fraction was closed to about 80percents of DOC found in the GAC influent. The Number-average molecular weight (Mn) value determined using HPSEC for the effluent of GAC column was gently increased as DOC breakthrough progress. The quotient p(Mw/Mn) can be used to estimate the degree of polydispersity was shown greatest value for the GAC effluent at the initial stage of the RSSCT operation.

• Polymer(Korea)
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• v.33 no.5
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• pp.463-468
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• 2009

Syntheses of monodisperse and micron-sized hollow plastic pigment (HPP) were carried out through the core-shell reaction. The effects of the reaction parameters, such as the particle size, molecular weight, the swelling time, agitation rate, and the solid contect were investigated. This micron-sized HPP could be made by using the alkali soluble core with at least bigger than 200 nm size. To obtain a higher opacity ratio, the swelling time and molecular weight of the core should be controlled. The agitation rate affected the particle's morphology. To prevent the shell destruction, the agitation rate must be sufficiently low in case of the syntheses of micron-sized HPP. In this study, micron-sized HPP exhibiting the high hiding power and narrow particle distribution could be obtained.

• Polymer(Korea)
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• v.33 no.5
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• pp.458-462
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• 2009

We have synthesized ABC linear triblock copolymers, i.e., polystyrene-b-poly(ethylene oxide)-b-polylactide, via sequential anionic and ring-opening polymerizations. In the first anionic polymerization step, styrene was polymerized in cyclohexane using sec-butyllithium as the initiator. Poly (styryl) lithium was hydroxylated by the addition of ethylene oxide, and the subsequent protonation with methanolic HCl. In the second anionic polymerization step, potassium naphthalenide was used to deprotonate the hydroxyl group of the PS to generate the macroinitiator of PS-$O^-K^+$. Polymerization of ethylene oxide was performed in THF and terminated with methanolic HCl. In the ring-opening polymerization step, the PS-b-PEO-$AlEt_2$ macroinitiator was prepared from an $AlEt_3$/pyridine system in THF, and the polymerization of lactide was performed at $90^{\circ}C$. The resulting block copolymers showed well-defined molecular weights and narrow molecular weight distributions as revealed by $^1H$- NMR spectroscopy and gel permeation chromatography (GPC).

• Journal of Digital Convergence
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• v.13 no.4
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• pp.369-375
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• 2015

In this study, the formation potential and the stability of nano-emulsions were evaluated according to the structure of various cosmetic oils in Tween 80/Span 80 system using PIC method at 80 oC LP 70, Isopar H and Pripure 3759 of hydrocarbons were both form a stable nano-emulsion, particle size distribution of about 40 nm. A linear structure of silicone oil formed an unstable emulsion, but cyclic or short chain oil formed was a stable nano-emulsion. In ester oils, the particle size of emulsions increases with increasing molecular weight of oils and a stable nano-emulsion could not be obtained in the molecular weight of about 450. The particle size of the nano-emulsion against required HLB value for calculating in consideration of the lipophilic and hydrophilic oil was smaller in the HLB of 8-10.