• Clean Technology
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• v.12 no.2
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• pp.62-66
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• 2006

Poly($\small{L}$-Lactide)(PLLA) was prepared by a ring-opening polymerization of $\small{L}$-Lactide with various polydimethylsiloxane(PDMS) based copolymers as a stabilizer in supercritical carbon dioxide($scCO_2$). The block copolymeric stabilizers were synthesized by group transfer polymerization (GTP) by using PDMS macroinitiator. PLLA was found to be produced with fairly low molecular weight distribution as confirmed by gel permeation chromatography(GPC) analysis. Scanning electron microscopy (SEM) results showed that sub-micron size Poly($\small{L}$-lactide)(PLLA) particles were formed by suspension polymerization.

• Polymer(Korea)
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• v.28 no.2
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• pp.143-148
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• 2004

${\alpha}$,$\omega$-Hydrogen polyorganosiloxane(HPMDMS) prepolymer was prepared from equilibrium polymerization ofoctamethylcyclotetrasiloxane, 1,3,5-trimethylcyclotrisiloxane, 1,3,5,7-tetravinyl-1,3,5,7-tetramethyl-cyclotetrasiloxane, and 1,1,3,3-tetramethyl disiloxane as an end-blocker in the presence of tetramethylammonium siloxanolate as a catalyst. Polyorganosiloxane modified with dimethylacrylamide(APMDMS) was prepared by hydrosilylation of HPMDMS with dimethylacrylamide in the presence of Pt catalyst, and followed by coordination of metal oxide (APMDMS-MO), such as NiO and FeO, to the amide moieties of the resulting polymer. The chemical structures of HPMDMS and APMDMS were confirmed by FT-IR and $^1$H-NMR analysis. Liquid silicone rubber containing metal oxide composite (LSRMO) was prepared by compounding APMDMS-MO, ${\alpha}$,$\omega$-vinylpolydimethylsiloxane, and a catalyst in a high speed dissolver. The thermal conductivity of LSRMO composite was determined to be 0.29 W/mK, and the volume resistivity exhibited a lower value than that of LSR composite. The mechanical and thermal properties of LSRMO and LSR composite were measured by UTM and TGA.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2010.06a
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• pp.136-136
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• 2010

본 연구에서는 귀금속 촉매 식각법을 이용하여 고효율의 태양전지 응용을 위한 p형 실리콘 와이어 어레이를 제조 하였다. 실리콘 와이어 어레이를 기판에서 분리하기 위해 고무 상의 고분자인 폴리디메틸실록산 (polydimethylsiloxane)을 스핀 코팅을 이용하여 실리콘 와이어 어레이 위에 증착하였다. 희석제의 함량과 스핀코팅의 회전수에 따라 폴리디메틸실록산의 박막두께를 조절하였으며, 기계적 방법으로 실리콘 와이어 어레이를 기판에서 분리할 수 있음을 보여주었다.

• Polymer(Korea)
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• v.28 no.4
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• pp.305-313
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• 2004

A vacuum pressure-difference technique for making a nano-precision replica is investigated for various applications. Master patterns for replication were fabricated using a nano-replication printing (nRP) process. In the nRP process, any picture and pattern can be replicated from a bitmap figure file in the range of several micrometers with resolution of 200nm. A liquid-state monomer is solidified by two-photon absorption (TPA) induced by a femto-second laser according to a voxel matrix scanning. After polymerization, the remaining monomers were removed simply by using ethanol droplets. And then, a gold metal layer of about 30nm thickness was deposited on the fabricated master patterns prior to polydimethylsiloxane molding for preventing bonding between the master and the polydimethylsiloxane mold. A few gold particles attached on the polydimethylsiloxane stamp during detaching process were removed by a gold selecting etchant. After fabricating the polydimethylsiloxane mold, a nano-precision polydimethylsiloxane replica was reproduced. More precise replica was produced by the vacuum pressure-difference technique that is proposed in this paper. Through this study, direct patterning on a glass plate, replicating a polydimethylsiloxane mold, and reproducing polydimethylsiloxane replica are demonstrated with a vacuum pressure-difference technique for various micro/nano-applications.

• Proceedings of the Korean Fiber Society Conference
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• 1993.06a
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• pp.60-60
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• 1993

• Journal of the Korean Applied Science and Technology
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• v.32 no.3
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• pp.546-567
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• 2015

Silicone-based surfactants consist of a hydrophobic organosilicone group coupled to one or more hydrophilic polar groups, while the hydrophobic groups of hydrocarbon surfactants are hydrocarbons. Silicone surfactants have been widely used in many industrial fields starting from polyurethane foam to construction materials, cosmetics, paints & inks, agrochemicals, etc., because of their low surface tension, lubricity, spreading, water repellency and thermal and chemical stability. A wide range of silicone surfactant structures are required to provide the functional diversity for reflecting the necessities in the various applications. This review covers the basic properties and the synthetic schemes of polydimethylsiloxane and reactive polysiloxanes as hydrophobic siloxane backbones, the main reaction schemes, such as hydrosilylation reaction, for coupling reactive polysiloxanes to hydrophilic groups, and the synthetic schemes of the main polysiloxane surfactants including polyether-, ionic-, carbohydrate-type surfactants.

• Polymer(Korea)
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• v.37 no.2
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• pp.167-176
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• 2013

Linear and cross-linked waterborne polyurethanes (WPUs) based on isophorone diisocyanate and mixed diols of poly(tetramethylene glycol)/hydroxyethyl-terminated polydimethylsiloxane (PDMS-OH) were synthesized with dimethylol propionic acid as an anionic component, trimethylolpropane as a cross-linking agent, and butanediol as a chain extender and characterized. The hydrophobicity, $T_g$, stress-strain behaviors of the linear or cross-linked siloxane-containing WPU (WPU-Si) films with different PDMS content were analyzed by using water contact shape analyzer, energy dispersive spectrometer, dynamic mechanical analyzer, and universal testing machine. The results reveal that as the PDMS content increased, the hydrophobicity of WPU-Si films increased, $T_g$ moved to higher temperature, the breaking stress increased, and the breaking strain decreased.

• Composites Research
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• v.30 no.2
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• pp.165-168
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• 2017

Coiled polymer actuators fabricated by twisting polymer fishing lines or sewing threads respond to heating and cooling with their contraction and relaxation. However, their actuation speed is highly dependent on the heating and cooling rates. In order to improve the actuation speed, the coiled polymer actuator was coated with polydimethylsiloxane composites. The introduction of multi-walled carbon nanotubes into the polydimethylsiloxane improved the actuation speed by about 13%.

• Textile Coloration and Finishing
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• v.5 no.1
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• pp.1-9
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• 1993

The polymethylhydrosiloxane(PMHS) was synthesized by the co-hydrolysis of methyldichlorophydrosilane and ethyl ether, also polydimethylsiloxane(PDMS) was synthesized by the hydrolysis of dimethyl dichlorosilane and ethyl ether. The silk fabrics were treated with PMHS and PDMS in order to improve the water repellency and the wrinkle recovery. Also the effect of PMHS concentration, PDMS concentration and cure temperature on the physical properties of silk fabrics were studied. The maximum water repellency and maximum wrinkle recovery were obtained from the fabrics treated under the conditions 5%-PMHS and PDMS at 16$0^{\circ}C$, and 3%-PMHD and PDMS at 16$0^{\circ}C$, respectively. The tensile strength, the breaking elongation, the reflection and the bending properties of silk fabrics were not degraded severely by the treatment of PMHS or PDMS.

• Journal of the Korean Applied Science and Technology
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• v.32 no.2
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• pp.232-239
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• 2015

In this paper, we study the dry transfer technology utilizing PDMS (Polydimethylsiloxane) stamp of a large single-layer graphene grown on Cu-foil as catalytic metal by using Chemical Vapor Deposition (CVD). By changing the surface property of the target substrate through $UV/O_3$ treatment, we can transfer the graphene on the target substrate while minimizing mechanical damages of graphene layer. Multi-layer (1~4 layers) graphene was stacked on $SiO_2/Si$ wafer successfully by repeating thetransfer method/process and then optical transmittance and sheet resistance of graphene layers have been measured as a quality assessment.