• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2009년도 학술발표대회
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• pp.90-91
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• 2009

• 한국염색가공학회지
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• 제32권1호
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• pp.19-26
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• 2020

The previous study reported that the quaternary copolymer of MMA, BA, MAA, and NEA was expected to be a good monomer composition for a binder polymer with good rubbing fastness for digital textile printing(DTP) pigment ink. However, the rubbing fastness of the dyed fabric with the quaternary copolymer binder containing pigment ink is not enough to be commercially used. Therefore, this study aims to optimize MMA:BA:MAA:NEA composition for improved rubbing fastness. And the binder polymer with various MMA:BA:MAA:NEA compositions were synthesized using miniemulsion polymerization. The particle size, viscosity, molecular weight, and Tg of the synthesized binder were evaluated. And the color strength and rubbing fastness of the black pigment ink dyed cotton fabrics with the prepared binders were also evaluated. Then, the stiffness of undyed and dyed cotton fabrics were evaluated to investigate the changes in touch as the binder structure changes.

• 한국염색가공학회지
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• 제30권4호
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• pp.256-263
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• 2018

The binder polymers for digital textile printing(DTP) pigment inks were prepared using miniemulsion polymerization with various monomer compositions to study effects of monomer compositions on particle size distribution, average molecular weight, Tg, and color strength and rubbing fastness of the dyed fabrics with the prepared binder based pigment ink. The monomers used were MMA(Methyl methacrylate), BA(Butyl acrylate), MAA(Methacrylic acid), NMA(N-methylol acrylamide), NEA(N-ethylol acrylamide) and the ratios of the monomers were changed. The particle size was the smallest with 136nm when the MMA to BA weight ratio was 4:16 and the largest with 290nm when the MMA, BA, MAA, NEA ratio was 2.5:17:0.25:0.25. However, the glass transition temperature was lowest with $-41.90^{\circ}C$ and the color strength and rubbing fastness of the resulting sample were the best when the MMA, BA, MAA, NEA ratio was used. This suggested that the introduction of the NEA monomer to the binder polymer for the pigment ink could be an efficient way to enhance the rubbing fastness of the DTP pigment inks present.

• 한국염색가공학회지
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• 제31권2호
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• pp.77-87
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• 2019

To improve rubbing fastness of the printed fabrics, the binder polymers for Digital Textile Printing(DTP) pigment inks were synthesized with miniemulsion polymerization using various acrylic monomers, which are MMA(Methyl methacrylate), BA(Butyl acrylate), and Self-crosslinking monomers, such as NEA(N-Ethylol acrylamide) and MAA (Methacrylic acid). The acrylic monomer compositions were varied when synthesizing the binder polymers and their particle size distributions, average molecular weights, and Tgs were investigated. The prepared binder polymers were applied to prepare Cyan, Black, Yellow and Magenta pigment ink for DTP and the prepared inks were used to dye cotton fabrics. Then, color strength, and rubbing fastness were also investigated to study the effect of the comonomer compositions of the binder polymer on the color strength and rubbing fastness of the resulting pigment inks.

• 폴리머
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• 제37권1호
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• pp.15-21
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• 2013

폴리스티렌을 쉘 물질로 하여 상변환물질인 파라핀 왁스 코어 물질을 나노캡슐화하는 방법과 형성된 입자들의 열적 특성을 연구하였다. 나노캡슐화의 방법으로는 미니에멀젼 중합법을 채택하였다. 중합시 사용된 가교제의 성질, 유화제의 양, 상변환 물질과 단량체의 비율, 개시제의 친수성 등이 나노캡슐화된 상변환물질의 열적 특성에 미치는 영향을 분석하였다. 오스왈드 숙성에 의한 입자의 크기 변화, 형태 변화는 캡슐 입자의 열적 특성에 가장 큰 영향을 미치는 것으로 나타났으며, 또한 폴리스티렌 쉘의 친수성과 가교밀도도 캡슐 입자의 형태 변화와 이로 인한 열적 특성에 영향을 주는 것으로 나타났다.

• 접착 및 계면
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• 제24권1호
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• pp.1-8
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• 2023

공액고분자는 유기전자소자부터 바이오메디칼 응용분야까지 다양하게 적용가능한 차세대 반도체소재이다. 하지만 낮은 수용성으로 주로 유기용매에 녹여 사용하나 최근 유기 용매의 독성과 환경 문제 이슈로 공액고분자의 수분산 나노입자화가 주목받고 있다. 본 총설에서는 나노입자가 형성되는 두 가지 원리와 이를 이용한 대표적인 공액고분자 나노입자 합성방법들 및 관련 연구들을 소개하고자 한다.

• Macromolecular Research
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• 제15권1호
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• pp.51-58
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• 2007

The approach studied in the present work produced an exfoliated state of clay layers via confinement of the charged nano-sized polystyrene (PS) beads within the gallery of swollen pristine clay. It was demonstrated that adsorption of the polymer nanobeads dramatically promotes expansion of the clay gallery. A comparative study of incorporation was conducted by employing organo-modified clay along with two different colloid polymer systems: electrostatically stabilized PS nanobeads and cationic monomer-grafted PS nanobeads. The mechanism of adsorption of the monomer-grafted polymer beads onto clay via cationic exchange between the alkyl ammonium group of the polymer nanobeads and the interlayer sodium cation of the layered silicate was verified by using several techniques. As distinct from the polymer nanobeads formed using conventional miniemulsion polymerization method, competitive adsorption of stabilizing surfactant molecules was be prevented by grafting the surface functional groups into the polymer chain, thereby supporting the observed effective adsorption of the polymer beads. The presence of surface functional groups that support the establishment of strong polymer-clay interactions was suggested to improve the compatibility of the clay with the polymer matrix and eventually play a crucial role in the performance of the final nanocomposites.

• 한국염색가공학회지
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• 제31권4호
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• pp.341-353
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• 2019

Quercetin is one of flavonoids widely distributed in the plants and well known to have antioxidants, antiinflammatory, antimicrobial properties. In this study, alginate sponge containing quercetin-encapsulated nanocapsules was prepared by miniemulsion polymerization, dyring/crosslinking method and their bioactive characteristics were investigated. Alginate sponge containing quercetin-encapsulated nanocapsules were evaluated using a field emission scanning electron microscope(FE-SEM), a high performance liquid chromatography, cell viability, DPPH radical scavenging activity and antibacterial activity. The study indicates that alginate sponge containing quercetin-encapsulated nanocapsules had significant antioxidant, antiinflammatory and antibacterial activities. This study suggested that alginate sponge containing quercetin-encapsulated nanocapsules can be a potential candidate for medical materials.

• 폴리머
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• 제33권5호
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• pp.452-457
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• 2009

다중벽 탄소나노튜브 및 전도성 고분자인 PEDOT으로 이루어진 하이브리드 나노재료를 제조하였다. 다중벽 탄소나노튜브 표면에 처리반응을 수행함으로써 -Br 특성기를 갖는 다중벽 탄소나노튜브를 제조하였으며, 이를 중합반응의 개시제로 사용하였다. 이와 함께 MMA를 사용하여 촉매와 리간드 존재 하에서 원자이동 라디칼중합 공정을 수행함으로써 다중벽 탄소나노튜브 표면에 PMMA가 공유결합된 나노복합체를 제조하였다. 미니에멀젼 중합공정을 통하여 제조된 PS 수용성 에멀젼에 EDOT과 산화가를 투입하여 산화중합을 수행함으로써 core-shell 구조를 갖는 PEDOT/PS 나노입자를 제조하였다. 실란화합물로 표면 처리한 silica 입자를 PEDOT:poly(styrene sulfonate) (PSS) 수용성 분산액에 투입한 후 표면화학 반응과정을 수행함으로써 silica 외벽에 PEDOT:PSS가 코팅된 나노입자를 제조하였다. 하이브리드 나노재료들은 TEM, FE-SEM, TGA, EDX, UV 그리고 FT-IR 등을 사용하여 분석되었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2010년도 제39회 하계학술대회 초록집
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• pp.281-281
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• 2010

Very low refractive index (<1.4) materials have been proved to be the key factor improving the performance of various optical components, such as reflectors, filters, photonic crystals, LEDs, and solar cell. Highly porous SiO2 are logically designed for ultralow refractive index materials because of the direct relation between porosity and index of refraction. Among them, ordered macroporous SiO2 is of potential material since their theoretically low refractive index ~1.10. However, in the conventional synthesis of ordered macroporous SiO2, the time required for the crystallization of organic nanoparticles, such as polystyrene (PS), from colloidal solution into well ordered template is typical long (several days for 1 cm substrate) due to the low interaction between particles and particle - substrate. In this study, polystyrene - polyacrylic acid (PS-AA) nanoparticles synthesized by miniemulsion polymerization method have hydrophilic polyacrylic acid tails on the surface of particles which increase the interaction between particle and with substrate giving rise to the formation of PS-AA film by simply spin - coating method. Less ordered with controlled thickness films of PS-AA on silicon wafer were successfully fabricated by changing the spinning speed or concentration of colloidal solution, as confirmed by FE-SEM. Based on these template films, a series of macroporous SiO2 films whose thicknesses varied from 300nm to ~1000nm were fabricated either by conventional sol - gel infiltration or gas phase deposition followed by thermal removal of organic template. Formations of SiO2 films consist of interconnected air balls with size ~100 nm were confirmed by FE-SEM and TEM. These highly porous SiO2 show very low refractive indices (<1.18) over a wide range of wavelength (from 200 to 1000nm) as shown by SE measurement. Refraction indices of SiO2 films at 633nm reported here are of ~1.10 which, to our best knowledge, are among the lowest values having been announced.