• 제목/요약/키워드: Interfacial polymerization

검색결과 104건 처리시간 0.023초

저온 플라즈마 처리에 의한 전자파 차폐성 금속화 합성섬유의 계면 밀착성 개선 (Improvement of Interfacial Adhesion of Metal Plated Synthetic Fabrics for Electromagnetic Wave Shielding by Using Cold Plasma)

  • 천태일
    • 한국염색가공학회지
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    • 제10권2호
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    • pp.8-17
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    • 1998
  • In this study we have examined electroless chemical plating on the plasma grafted poly [ethylene terephathalate](PET) fabric in order to improve the interfacial adhesion between metal and fiber. The vapour phase of acrylic acid introduced on the PET surface and the graft polymerization was carried out by using cold plasma, resulting in the grafting yield of 0.8-1.3 wt%. The carboxyl group of the plasma grafted was identified by FT-IR-ATR spectra. The Interfacial adhesion was related to the carboxyl group. After electroless chemical plating of nickel, it showed that the more the carboxyl, the better the interfacial adhesion. Comparing to the untreated, the plasma grafted fabric showed fairly good interfacial adhesion(5B grade, ASTM D3359) . The shielding effect of electromagnetic wave showed 95dB. The shielding effect depends on the fabric structure, the surface structure, and the cross sectional shape of fibers. The dense fabric structure, the etched surface like a microcrater, and the trigonal cross sectional shape were prefered.

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기능성 microsphere의 개발(II) - EVA Microsphere의 표면개질과 특성 - (Development of Functional Microsphere( II ) - Surface Modification and Properties of EVA Microsphere -)

  • 김혜인;박형섭;박수민
    • 한국염색가공학회지
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    • 제17권3호
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    • pp.26-33
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    • 2005
  • EVA microsphere was prepared by a thermally induced phase separation. EVAL microsphere was made by a saponification on sheath of EVA microsphere. And microcapsule with EVA core-PU shell structure was synthesized by interfacial polymerization using diisocyanates with PEG in gelatin aqueous solution as the stabilizing agent. The effects of chemical structure of diisocyanate on the average particle size and distribution, morphology, color strength and friction fastness of core-shell particles were investigated to design microcapsule. The friction fastness of the fabrics printed with EVA core-PU shell microcapsules had the 4-5 grade.

Nanofiltration of Dye Solutions Through Polyamide Composite Membranes

  • Jonggeon Jegal;Baek, Kyung-Sook;Lee, Kew-Ho
    • Korean Membrane Journal
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    • 제4권1호
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    • pp.12-19
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    • 2002
  • Nanofiltration of aqueous dye solutions was carried out using polyamide (PA) nanofiltration (NF) composite membranes. The PA composite membranes were prepared by the interfacial polymerization of piperazine (PIP) and trimesoyl chloride (TMC) on the surface of microporous polysulfone (PSf) ultrafi1tration (UF) membranes. After characterization in terms of their permeation performance and surface ionic property, they were used for the separation of dye solutions such as Direct Red 75, 80, 81, and Direct Yellow 8 and 27. The separation conditions were varied to study the factors affecting on the permeation performance of the membranes: different concentrations of dye solutions, operating temperature and time, and flow rate of a feed solution. The surface property of the membrane, especially its ionic property, as a function of operating time was examined with a zeta-potentiometer and the relationship between the surface chemistry of the membrane and its permeation properties was also studied.

표면 개질된 나노복합막의 투과 특성 (Permeation Properties of Surface Modified Nanofiltration Membrane)

  • 탁태문;박형규;장경국
    • 멤브레인
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    • 제14권3호
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    • pp.207-217
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    • 2004
  • 본 연구에서는 복합막의 제조공법으로 가장 광범위하게 쓰이는 계면중합법을 이용하여 나노복합막을 제조하였다. Monomer의 농도 및 조성, curing 조건, 후처리 조건과 같은 복합막 제조조건과, 운전압력, 공급액의 농도와 같은 운전인자에 의한 막성능 변화를 조사하였고, 계면중합 과정중에 첨가제를 사용하여 막의 유효면적을 확대하여 투과유속을 증가시키고자 하였다. Monomer의 농도가 증가함에 따라 배제능은 일정하였지만 투과유속이 감소하였고, curing 온도가 증가함에 따라서는 오히려 안정적인 박막층의 형성이 저해되어서 배제능과 투과유속이 모두 감소하였고, curing 시간에 따른 막성능의 변화는 나타나지 않았다. Test solution의 농도가 올라감에 따라서 투과유속과 배제능 모두 감소하였으며, 운전압력이 증가함에 따라서는 배제능과 투과유속 모두 향상하는 경향을 보였다. 계면중합과정중에 사용하는 아민단량체(amine monomer) 중 방향족 다이아민(aromatic amine)인 MPD의 함량을 높임에 따라서 배제능은 증가하였지만 투과유속은 현저하게 떨어졌다. 첨가제의 농도에 따른 표면 거칠기 증가 경향은 MPD가 포함된 amine 조성일 때가 더 높았지만 투과유속은 piperazine만 단독으로 사용하였을 때보다 떨어졌다.

계면중합에 의한 역삼투용 복합막 제조에 관한 연구 (Manufacture of the Thin-Film Composite Membranes for the Reverse Osmosis Process using Interfacial Polymerization Technique)

  • 박종원;김희진;민병렬
    • 멤브레인
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    • 제8권1호
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    • pp.29-41
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    • 1998
  • 수용상 MPD(m-phenylene diamine)와 유기상 TMC(trimesoyl chloride)를 사용하여 역삼투 복합막의 활성층 고분자인 aromatic polyamide 제조를 행하고 그 성능을 고찰하였다. 또한 polysulfone 다공성 지지막 위에 박막을 회분, 연속식으로 계면중합 제조한 후, 제조변수에 따른 역삼투 성능을 비교하였다. 회분식으로 복합막을 제조한 결과 유기상 용매의 종류, 단량체의 농도와 함침시간, 열처리 온도, 중화제, 알코올 후처리, 산 후처리 등에 의해 다양한 성능을 나타내었다. 이때, 투과량 향상에는 알코올 후처리 효과가, 또 선택도의 향상에는 단량체의 농도와 함침시간이 변수이었다. 최적조건에서 연속식 공정으로 막모듈을 제조하여 NaCl 5,000 ppm, $25kg_f/cm^2$에서 상용막과 비교할때, 투과량은 33% 증가하고 배제율은 5% 감소하였다.

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다공성 PVDF 막의 polyamide 계면중합법처리를 통한 나노 중공사 복합막 제조 연구 (Study on the Hollow Fiber Nano-composite Membrane Preparation onto the Porous PVDF Membrane Surfaces using the Interfacial Polymerization)

  • 강수연;조은혜;김일형;김정식;임지원
    • 멤브레인
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    • 제24권2호
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    • pp.107-112
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    • 2014
  • Poly (vinylidene fluoride) (PVDF)의 소수성 중공사막 표면에 계면중합하여 복합막을 제조하였다. Piperazine (PIP)과 trimesoyl chloride (TMC)의 농도변화, polyethylene glycol (PEG)의 함량변화에 따라 막을 제조하였으며, 막의 특성 평가를 위해 100 ppm의 NaCl, $CaSO_4$, $MgCl_2$ 용액과 NaCl과 $CaSO_4$를 혼합하여 제조한 300 ppm의 공급액에 대한 막의 투과도와 배제율을 알아보고자 하였다. TMC를 사용하여 계면중합하였을 때 막의 투과도와 배제율이 가장 높게 나타났으며, 0.1~1 wt%로 TMC 농도를 변화시켜 가며 실험을 수행한 결과 0.1 wt%일 때 NaCl 100 ppm에 대해 투과도 48.3 LMH ($L/m^2{\cdot}hr$)와 배제율 59%로 가장 높은 값을 나타내었다. 또한, 투과도를 향상시키기 위해 annealing처리와 piperazine에 PEG를 첨가하여 실험을 수행하였다. 실험결과 처리하지 않은 막에 비해 투과도는 전체적으로 향상되는 모습을 나타냈지만 배제율이 감소하는 경향을 나타내었다.

狀移動重合. Tetrabutylammonium Bromide 존재하에서 Diphenoxides와 1,6-Dibromohexane의 二狀重縮合反應 (Phase Transfer Polymerization. Two Phase Polycondensation of Diphenoxides and 1,6-Dibromohexane in the Presence of Tetrabutylammonium Bromide)

  • 진정일;정용운;이광섭;정근우
    • 대한화학회지
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    • 제23권4호
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    • pp.259-266
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    • 1979
  • 수용액상에 존재하는 2,2-비스(4-히드록시페닐)프로판, 황화비스(4-히드록시페닐) 및 비스(4-히드록시페닐)술폰의 음이온과 니트로벤젠속에 존재하는 1,6-디브르모헥산을 브롬화테트라부틸 암모늄을 상이동 촉매로 사용하여 반응시켜 새로운 폴리에테르를 합성하였다. 중합속도는 교반속도와 촉매량에 의존하였으나 어느정도 이상에서는 영향을 받지 않았다. 분배실험으로 부터 친수성 음이온이 촉매에 의하여 니트로벤젠 층으로 상이동함을 확증하였으며 일부 중합체의 본성점성도 (0.09∼0.16), 수평균분자량 (2400∼4800) 및 열안정성등을 조사하였다. 이와같은 중합 메카니즘은 소위 interfacial polymerization의 메카니즘과 다르며, 이를 구별하기 위하여 "상이동 중합''(phase transfer polymerization) 이란 용어를 사용할 것을 제안한다.

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Core-Shell Polymerization with Hydrophilic Polymer Cores

  • Park, Jong-Myung
    • Macromolecular Research
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    • 제9권1호
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    • pp.51-65
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    • 2001
  • Two-stage emulsion polymerizations of hydrophobic monomers on hydrophilic seed polymer particles were carried out to make core-shell composite particles. It was found that the loci of polymerization in the second stage were the surface layer of the hydrophilic seed latex particles, and that it has resulted in the formation of either eccentric core-shell particles with the core exposed to the aqueous phase or aggregated nonspherical composite particles with the shell attached on the seed surface as many small separated particles. The driving force of these phenomena is related to the gain in free energy of the system in going from the hydrophobic polymer-water interface to hydrophilic polymer-water interface. Thermodynamic analysis of the present polymerization system, which was based on spreading coefficients, supported the likely occurrence of such nonspherical particles due to the combined effects of interfacial free energies and phase separation between the two polymer phases. A hypothetical pathway was proposed to prepare hydrophilic core-hydrophobic shell composite latex particles, which is based on the concept of opposing driving and resistance forces for the phase migration. It was found that the viscosity of the monomer-swollen polymer phase played important role in the formation of particle morphology.

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Preparation of novel NF membrane via interfacial cross-linking polymerization

  • Lehi, Arash Yunessnia;Akbari, Ahmad;Soleimani, Hosna
    • Membrane and Water Treatment
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    • 제6권3호
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    • pp.173-187
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    • 2015
  • The goal of present work is the preparation of a novel positively charged nanofiltration (NF) membrane and its development for the cation removal of aqueous solutions. This NF membrane was fabricated by the surface modification of polysulfone (PSf) ultrafiltration support. The active top-layer was formed by interfacial cross-linking polymerization of poly(ethyleneimine) (PEI) with p-xylylene dichloride (XDC) and then quaternized with methyl iodide to form a perpetually positively charged layer. In order to improve the efficiency of nanofiltration membrane, the concentration of PEI, XDC and methyl iodide solutions, PEI coating and cross-linking time have been optimized. As a result, a high water flux and high $CaCl_2$ rejection (1,000 ppm) was obtained for the composite membrane with values of $18.29L/m^2.h$ and 93.62% at 4 bar and $25^{\circ}C$, respectively. The rejections of NF membrane for different salt solutions followed the order of $Na_2SO_4$ < $MgSO_4$ < NaCl < $CaCl_2$. Molecular weight of cut off (MWCO) was calculated via retaining of PEG solutions with different molecular weights that finally, it revealed the Stokes and hydrodynamic radius of 1.457 and 2.507 nm on the membrane selective layer, respectively. The most efficient positively charged nanofiltration membrane exhibited a $Ni^{2+}$ rejection of 96.26% for industrial wastewater from Shamse Hadaf Co. (Kashan, Iran).