• Title/Summary/Keyword: Silane modification

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Spectroscopic Analysis of Silica Nanoparticles Modified with Silane Coupling Agent (실란 커플링제에 의해 표면이 개질된 실리카 나노입자의 분광학적 분석)

  • Song, Seong-Kyu;Kim, Jung-Hye;Hwang, Ki-Seob;Ha, Ki-Ryong
    • Korean Chemical Engineering Research
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    • v.49 no.2
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    • pp.181-186
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    • 2011
  • In this study, we used 3-(trimethoxysilyl)propylmethacrylate(MPS) silane coupling agent for surface modification of silica nanoparticles. We studied effects of reaction conditions such as solvent pH, MPS hydrolysis time, reaction time, and molar ratio of MPS to Si-OH groups on silica nanoparticle surfaces, on the surface modification reactions of silica nanoparticles. Fourier Transform Infrared Spectroscopy(FTIR), Elemental Analysis(EA) and solid state crosspolarization magic angle spinning(CP/MAS) Nuclear Magnetic Resonance Spectroscopy(NMR) techniques were used to determine the type and the degree of surface modification. We found MPS reacts preferentially with Si-OH groups of the silica nanoparticles as monomeric form at solvent pH = 4.5. But increasing hydrolysis time of MPS from 30 mins to 90 mins, and molar ratio of MPS to Si-OH groups on silica nanoparticle surfaces, we found that MPS reacts preferentially with Si-OH groups of the silica nanoparticles as oligomeric form.

Effect of Surface Modification of Calcium Carbonate Nanoparticles by Octyltrimethoxysilane on the Stability of Emulsion and Foam (실란 커플링제 옥틸트리메톡시실란에 의해 표면 개질된 탄산칼슘 나노입자가 에멀젼 및 기포 안정성에 미치는 영향)

  • Lim, Jong Choo;Park, Ki Ho;Lee, Jeong Min;Shin, Hee Dong
    • Applied Chemistry for Engineering
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    • v.33 no.4
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    • pp.386-393
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    • 2022
  • In this study, the surface modification of calcium carbonate (CaCO3) nanoparticles by a silane coupling agent, octyltrimethoxysilane (OTMS), was investigated and characterized using Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA) analysis. Both floating tests and contact angle measurements were also conducted to study the effect of OTMS concentration on the hydrophobicity of CaCO3 nanoparticles. It was found that the active ratio for the CaCO3 nanoparticles modified by 1 wt% of OTMS was 97.0 ± 0.5%, indicating that OTMS is a very effective silane coupling agent in enhancing the hydrophobicity of the CaCO3 nanoparticle surface. The most stable foam was generated with 1 wt% of CaCO3 nanoparticles in aqueous solutions at 1 wt% of OTMS, where the contact angle of water was found to be 91.8 ± 0.7°. It was also found that the most stable emulsion drops were formed at the same OTMS concentration. These results suggest that CaCO3 nanoparticles modified by a silane coupling agent OTMS are a powerful candidate for a foam stabilizer or an emulsifier in many industrial applications.

Preparation and Characterization of ACF Using Lyocell Adopting Surface Modification Process (리오셀 표면개질공정을 도입한 ACF 제조 및 특성)

  • Jo, Young Hyuk;Jin, Young Min;Lee, Soon Hong
    • Journal of the Korean Society of Safety
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    • v.31 no.1
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    • pp.66-73
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    • 2016
  • Lyocell fibers were used as a precursor in order to improve yield and strength of cellulose-based precursor while manufacturing activated carbon fiber(ACF). Lyocell fibers as a precursor for the preparation of ACF were surface-modified by reaction with 3-aminopropyltriethoxysilane(APTES) and pre-treated with KOH and H3PO4. Using aforementioned precursor, ACFs were prepared by a series of stabilization, carbonization and activation process at high temperatures. On each process, FT-IR, TGA, UTM and SEM were used to observe fibers' physical properties including structure and porous surfaces. FT-IR results proved that surface modification was achieved during stabilization, carbonization and activation process. TGA results during carbonization process found that surface modified fibers with APTES 0.02 mol(A2) showed higher thermostability, and extended pre-treatment increased yield. Especially, yield was found to have an increase of 10~20 wt% with surface modification during activation process. UTM results showed that tensile strength has the same order of concentration of APTES after surface modification, however, was found to show lower tensile strength than lyocell fibers after stabilization process. SEM results revealed that more homogeneous porosity control could be proceed after modifying the surface for the effective removal of hazardous substances.

Surface modification of plastic substrates mediated by silane coupling agents and its application for plastic assembly (use poster) (실란 화합물 기반 플라스틱 기판의 표면 개질화 및 저온 저압 접합 공정)

  • Lee, Nae-Yun
    • Proceedings of the Korean Institute of Surface Engineering Conference
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    • 2013.05a
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    • pp.107-108
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    • 2013
  • 플라스틱 기판 표면을 플라즈마 처리시 형성되는 수산화기에 실란화합물을 반응시키면 상온에서도 플라스틱 표면에 다양한 유기기를 도입할 수 있다. 아민기와 에폭시기가 상온에서도 강력한 화학결합을 이루는 원리를 이용하여, 유기기로써 아미노기와 에폭시기를 갖는 두 실란화합물을 선정, 두 고분자 기판에 각각 도입 후 접합시킨 결과, 저온 및 대기압 조건에서도 강력한 본딩을 이루는 것을 확인할 수 있었다.

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Improvement of Fouling Resistance with Reverse Osmosis Membrane Using Multi-layer Silane-Epoxy Surface Modification (실란-에폭시 다층 표면개질을 통한 역삼투막의 내오염성 향상)

  • Kwon, Sei;Lee, Yong Taek
    • Membrane Journal
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    • v.25 no.4
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    • pp.332-342
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    • 2015
  • In this study, to solve the major problem of reverse osmosis (RO) membrane, surface of reverse osmosis membrane was modified by silane-epoxy multi layer. Octyltrimethoxysilane (OcTES) was polymerized to membrane surface via cross-linking by Sol-gel method. n = 8 alkylgroup of OcTES formed the branch structure by self assembly. And for improve fouling resistance of RO membrane, Ether group of ethylene glycol diglycidyl ether (EGDE) was given to improve hydrophilicity of RO membrane surface by ring-opening. To analyze structure of RO membrane surface with FE-TEM and AFM. Membrane surface of the ridge and valley structure and the bridge structure was confirmed due to the multi-layer surface modification of OcTES and EGDE. And through the increase of the roughness, the branch structure was formed well on membrane surface. Through the XPS analysis was identified chemical structure of membrane surface. And confirmed that the hydrophilic surface modification is given to the surface of the film through a Contact angle analysis. In optimization of EGDE surface modification condition, was suitable 0.5 wt% EGDE concentraion and $70^{\circ}C$ ring-opening temperature. In result of fouling resistance test and MFI is SUL-H10, $PA-OcTES_{1.0}$, $PA-OcTES_{1.0}-EGDE_{0.5}$ 68.7, 60.4, 5.4 ($10E-8hr/mL^2$), multi-layer surface modified membrane improved fouling resistance.

Influence of Reinforcing Systems on Thermal Aging Behaviors of NR Composites (충전 시스템이 NR 복합체의 열노화 거동에 미치는 영향)

  • Choi, Sung-Seen;Kim, Jong-Chul
    • Elastomers and Composites
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    • v.46 no.3
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    • pp.237-244
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    • 2011
  • Five natural rubber (NR) composites with different reinforcing systems of unfilled, carbon black, carbon black with silane coupling agent, silica, and silica with silane coupling agent were thermally aged and change of the crosslink densities by the accelerated thermal aging was investigated. The crosslink densities on the whole increased as the aging time elapsed irrespective of the reinforcing systems. The crosslink density changes became noticeable by increasing the aging temperature. For carbon black-filled composites, the silane coupling agent made the crosslink density change to be increased. For silica-filled composites, however, the silane coupling agent made the crosslink density increment reduced at 60 and $70^{\circ}C$ and it hardly affect the degree of the crosslink density change at 80 and $90^{\circ}C$. The activation energies for the crosslink density changes of the carbon black-filled samples increased continuously in a logarithmic fashion, whereas that of the silica-filled one showed a quasi-steady state ranges at aging times of 30-150 days. The activation energy of the unfilled sample increased exponentially with the aging time. The experimental results were explained with sulfur donation from the silane coupling agent, surface modification of the filler by the silane coupling agent, adsorption of curative residues on the silica surface, and release of the adsorbed curative residues.

폴리에스테르 바니시에서 나노 실리카의 분산성 향상과 나노 복합체 에나멜 와이어 개발

  • Kim, Yong-Beom;Kim, Eun-Jin;Kim, Seon-Jae;Hwang, Jong-Seon;Choe, Yong-Seong;Seo, Yeong-Su
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2009.11a
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    • pp.151-151
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    • 2009
  • A enameled wire may have better corona-resistance when its coating material contains nano-sized inorganic particles. However, industrial applications are still limited because an aggregation between nanofillers may happen during coating processes. In this study we use a novel scheme of surface modification with silane on silica nanoparticles using sonochemical reaction where composition and surface density of silanes can be controlled in order to reduce particle-particle attractive interaction. Functionalized nanoparticles are evenly dispersed in the matrix confirmed by SEM and energy dispersive x-ray analysis. Dielectric strength and thermal resistance of the nanocomposite wires are improved while flexibility of the wire maintains.

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Preparation and Characterization of Chemically Modified Wood Flour Reinforced Phenol-formaldehyde Composites

  • Nam, Byeong-Uk;Mun, Jun-Yeong
    • Journal of the Semiconductor & Display Technology
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    • v.17 no.1
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    • pp.1-5
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    • 2018
  • Wood Polymer Composites(WPC) have attracted significant attention because of ecological and environmental concerns. However, the structure of Wood Flour containing many hydroxyl groups(-OH) reduces the interface adhesion to Phenol-formaldehyde(PF) and it decreases the mechanical properties of the PF/Wood Flour Composites. The present work involves the modification of Wood Flour using silanes reinforced with Phenol-formaldehyde to enhance the mechanical properties of the composites. The spectroscopic properties of the composites were analyzed using FT-IR, XPS(X-ray Photoelectron Spectroscopy) and the mechanical properties i.e., tensile strength, flexural strength and impact strength were studied. We confirmed the modification effect of silanes by spectroscopic analysis, and the mechanical properties of the composites using wood flour modified by silanes were significantly improved.

Investigation of Co-poly-para-aramid Fiber Dispersion in Chloroprene Rubber Matrix and Improvement of Dispersibility Through Fiber Surface Modification

  • Garam Park;Hyeri Kim;Gayeon Jeong;Dohyeong Kim;Seungchan Noh;Dajeong Gwon;Myung Chan Choi;Jaseung Koo
    • Elastomers and Composites
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    • v.57 no.4
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    • pp.175-180
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    • 2022
  • To produce a co-poly-para-aramid fiber (AF, Technora®)-reinforced neoprene rubber composite, dispersion of AF in a neoprene matrix is investigated. The AF is then surface-modified by mercerization and acetone, plasma, and silane treatments to improve dispersibility. Finally, an internal mixer process is used to disperse the surface-modified fibers in the neoprene rubber matrix.

Microencapsulation of Surface-modified Carbon Black by Miniemulsion Polymerization (미니유화중합법에 의한 표면개질된 카본블랙의 마이크로캡슐화)

  • Jang, Heang Sin;Hong, Jinho;Lee, Jeongwoo;Shim, Sang Eun
    • Korean Chemical Engineering Research
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    • v.46 no.4
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    • pp.669-675
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    • 2008
  • Carbon black has been widely used in composites, tonor resin, and ink materials. Since carbon black readily agglomerates, it is important to disperse carbon black in real applications. Aiming to improve dispersion stability, carbon black was chemically oxidized to possess hydroxyl groups using a phase transfer catalyst at room temperature. The modified carbon black (CB-OH) was grafted by a silane coupling agent, p-methylacryloxypropyltrimethoxysilane, to carry teminal vinyl groups. The modified carbon black was subsequently used in miniemulsion polymerization to achieve encapsulted core-shell structure. Finally, well-encapsulated carbon black by polymer was obtained in the size range of 100-500 nm. Throughout the polymerization, the effects of surface modification, types of monomers, initiators, and emulsifiers were investigated.