• 제목/요약/키워드: Membranes interface

검색결과 62건 처리시간 0.022초

온실기체 분리용 폴리이서설폰 비대칭 중공사 막의 제조 (Preparation of Asymmetric Folyethersulfone Hollow Fiber Membranes for Flue Gas Separation)

  • 김정훈;손우익;최승학;이수복
    • 멤브레인
    • /
    • 제15권2호
    • /
    • pp.147-156
    • /
    • 2005
  • 폴리이서설폰은 상용화된 엔지니어링 고분자 소재 중에서 이산화탄소/질소 및 이산화탄소/메탄의 분리 능력이 아주 우수하면서 이산화탄소에 대한 가소화에 대한 저항력이 아주 뛰어난 것으로 알려져 있다[1-4]. 본 연구에서는 연소 배가스내 이산화탄소의 분리/회수를 위하여 건-습식 상전이법에 의해 비대칭구조의 폴리이서설폰 중공사막을 제조하였다. 제막용액은 고비점이면서 폴리이서설폰의 용매인 NMP와 저 비점의 폴리이서설폰의 팽윤제인 acetone를 일정한 조성으로 함께 녹여서 제조하였다. 방사용액의 농도, NMP와 acetone의 비, 방사높이, 증발조건, 실리콘 코팅조건을 변화시키면서 중공사를 제조하였으며, 얻어진 중공사막의 이산화탄소와 질소에 대한 기체투과도와 선택도는 순수기체를 통하여 측정하였다. 최적의 PES 중공사막은 PES/Acetone/NMP = 30/35/35 $wt\%$ 방사용액과 실리콘의 코팅조건하에 제조된 것으로 폴리이서설폰 소재 자체의 고유선택도인 $30\~40$$CO_2/N_2$ 선택도를 보였으며 $25\~50$ GPU의 이산화탄소 투과플럭스를 보였다. 이러한 선택도와 투과도로부터 계산된 중공사 외표면의 선택층의 두께는 $0.1\;{\mu}m$였다. 제조된 폴리이서설폰중공사막이 향후 연소 배가스내 이산화탄소 분리/회수용 막분리 공정에 적용될 경우 우수한 결과를 보일 것으로 예측된다.

Liquid Crystal-based Imaging of Enzymatic Reactions at Aqueous-liquid Crystal Interfaces Decorated with Oligopeptide Amphiphiles

  • Hu, Qiongzheng;Jang, Chang-Hyun
    • Bulletin of the Korean Chemical Society
    • /
    • 제31권5호
    • /
    • pp.1262-1266
    • /
    • 2010
  • In this study, we investigated the use of liquid crystals to selectively detect the activity of enzymes at interfaces decorated with oligopeptide-based membranes. We prepared a mixed monolayer of tetra(ethylene glycol)-terminated lipids and carboxylic acid-terminated lipids at the aqueous-liquid crystal (LC) interface. The 17 amino-acid oligopeptide SNFKTIYDEANQFATYK was then immobilized onto this mixed monolayer through N-hydroxysuccinimide-activation of the carboxylic acid groups. We examined the orientational behavior of nematic 4-cyano-4'-pentylbiphenyl (5CB) after conjugation of the 17 amino-acid oligopeptide with the mixed monolayer assembled at the interface. Immobilization of the oligopeptide caused orientational transitions in 5CB, with a change from homeotropic (perpendicular) to tilted alignment, which was primarily due to the reorganization of the monolayer. The orientation of the 5CB molecules returned to its homeotropic state after contacting the interface containing ${\alpha}$-chymotrypsin, which can cleave the immobilized oligopeptide. Control experiments confirmed that the enzymatic activity of ${\alpha}$-chymotrypsin triggered the ordering transitions in the LC. These results suggest that the LC can provide a facile method for selective detection of enzymatic activity.

Carbonate Crystal Growth Controlled by Interfacial Interations of Artifical Cell Membranes

  • Goh, Dai-Young;Ahn, Dong-June
    • Biotechnology and Bioprocess Engineering:BBE
    • /
    • 제2권2호
    • /
    • pp.109-112
    • /
    • 1997
  • Morphology of carbonate crystals grown on the surface of artificial cell membranes was controlled by changing the interfacial chemistry. For octadecyltriethoxysilane (OTE) films with terminal methyl groups interacting little with an aqueous calcium carbonate solution calcite (104) crystals were formed. Polymerized pentacosadiynoic acid (PDA) films with terminal carboxylic acid groups induced deposition of calcite (012) crystals aligned along with each other within a polymer domain. On the other hand, stearyl alcohol (StOH) films with terminal hydroxyl groups induced deposition of aragonite crystals. When PDA was mixed with StOH, the 8:1 PDA:StOH (molar ratio) film produced dominating calcite (012) crystals without any crystal alignment, and the 4:1 mixture film produced minor calcite (012) crystals and major aragonite crystals. For the 2:1, 1:1, 1:2, and 1:4 mixture films, aragonite crystals were dominating. Hence, it is found that the chemical composition at the interface plays a very important role in controlling the morphology of deposited carbonate crystals.

  • PDF

Transport Analysis of olefins & nitrogen through PDMS membranes

  • Kim, Jeong-Hoon;Shin, Hyo-Jin;Choi, Seung-Hak;Park, In-Jun;Lee, Soo-Bok
    • 한국막학회:학술대회논문집
    • /
    • 한국막학회 2004년도 Proceedings of the second conference of aseanian membrane society
    • /
    • pp.195-198
    • /
    • 2004
  • Annually, 60 millions tons of polyolefins including polyethylene and polypropylene, etc. are produced in the world. During the manufacturing process, 1-2wt% of olefin gases of total feedstock remains unreacted and incinerated into air. Because of high cost of olefins and hazardous emission of carbon dioxide and toxic gases in incineration process, it is of important to recover them efficiently.(omitted)

  • PDF

Synthesis and characterization of polyamide thin-film nanocomposite membrane containing ZnO nanoparticles

  • AL-Hobaib, A.S.;El Ghoul, Jaber;El Mir, Lassaad
    • Membrane and Water Treatment
    • /
    • 제6권4호
    • /
    • pp.309-321
    • /
    • 2015
  • We report in this study the synthesis of mixed matrix reverse osmosis membranes by interfacial polymerization (IP) of thin film nanocomposite (TFNC) on porous polysulfone supports (PS). This paper investigates the synthesis of ZnO nanoparticles (NPs) using the sol-gel processing technique and evaluates the performance of mixed matrix membranes reached by these aerogel NPs. Aqueous m-phenyl diamine (MPD) and organic trimesoyl chloride (TMC)-NPs mixture solutions were used in the IP process. The reaction of MPD and TMC at the interface of PS substrates resulted in the formation of the thin film composite (TFC). NPs of ZnO with a size of about 25 nm were used for the fabrication of the TFNC membranes. These membranes were characterized and evaluated in comparison with neat TFC ones. Their performances were evaluated based on the water permeability and salt rejection. Experimental results indicated that the NPs improved membrane performance under optimal concentration of NPs. By changing the content of the filler, better hydrophilicity was obtained; the contact angle was decreased from $74^{\circ}$ to $32^{\circ}$. Also, the permeate water flux was increased from 26 to 49 L/m2.h when the content of NPs is 0.1 (wt.%) with the maintaining of lower salt passage of 1%.

Slippage on which interface in nanopore filtration?

  • Xiaoxu Huang;Wei Li;Yongbin Zhang
    • Membrane and Water Treatment
    • /
    • 제15권1호
    • /
    • pp.31-39
    • /
    • 2024
  • The flow in a nanopore of filtration membrane is often multiscale and consists of both the adsorbed layer flow and the intermediate continuum fluid flow. There is a controversy on which interface the slippage should occur in the nanopore filtration: On the adsorbed layer-pore wall interface or on the adsorbed layer-continuum fluid interface? What is the difference between these two slippage effects? We address these subjects in the present study by using the multiscale flow equations incorporating the slippage on different interfaces. Based on the limiting shear strength model for the slippage, it was found from the calculation results that for the hydrophobic pore wall the slippage surely occurs on the adsorbed layer-pore wall interface, however for the hydrophilic pore wall, the slippage can occur on either of the two interfaces, dependent on the competition between the interfacial shear strength on the adsorbed layer-pore wall interface and that on the adsorbed layer-continuum fluid interface. Since the slippage on the adsorbed layer-pore wall interface can be designed while that on the adsorbed layer-continuum fluid interface can not, the former slippage can result in the flux through the nanopore much higher than the latter slippage by designing a highly hydrophobic pore wall surface. The obtained results are of significant interest to the design and application of the interfacial slippage in nanoporous filtration membranes for both improving the flux and conserving the energy cost.

Membrane Concentrate Thickening by Hollow-fiber Microfilter in Drinkin Water Treatment Processes

  • 이병호
    • 멤브레인
    • /
    • 제1권1호
    • /
    • pp.100-100
    • /
    • 1991
  • A novel system to thicken the concentrated colloidal solution from membrane water treat-ment processes was developed. A hollow-fiber microfilter(hydrophilic polyethylene nominal pore size 0.1 μm total surface area 0.42 m2) was installed in an acrylic housing that has an aeration port 5 cm below the membrane and a clarifier in the bottom. The concentrate was uniformly supplied from the top of the housing. Bacuum filtration caused downward flow of concentrate and as a result thickening interface. The addition of poly-aluminum chloride (PAC) resulted in rapid increase of trans-membrane pressure (TMP) and in no improvement of the filtered water turbidity and thickening process. Two types of con-centrate and concentrate turbidity had little effect on the increase of TMP and concentrate thickening. It was observed that for the same height of membrane housing membrane surface area to housing volume (A/V) ratio had significant effect on the increase of TMP. When the housing volume was increased ten times the increasing rate of TMP was three times faster as compared to the original housing. A hydraulic model successfully simulated the formation and sedimentation of thickening interface.

자기기생하는 실새삼(Cuscuta australis)에서 세포 화합성에 관한 미세구조 연구 (Ultrastructural Study on the Cellular Compatibility in Self-Parasiting Cuscuta australis)

  • 이규배
    • Journal of Plant Biology
    • /
    • 제36권3호
    • /
    • pp.285-292
    • /
    • 1993
  • Cellular compatibility in the self-parasitism of Cuscuta australis R. Brown was studied at the ultrastructural level. The front cells of the haustorium penetrated the host stems independently grew within the host tissues and transformed into elongate, filamentous hyphae. Each hyphal cells contained a large nucleus and dense cytoplasm with abundant cell organelles. Multilamellar structures were contained in the cytoplasm and cell walls of the penetrating hyphal cells. When the hyphal cells did not yet invade the host cells, the middle lamella and the fused cellulosic cell walls of the two partners at the host-parasite interface were preserved well. As the invasion of the parasitic hyphal cells progressed, however, the middle lamella was not found at the interface and the host cell walls and plasma membranes were partially broken down. A hyphal cell penetrated deeply into the host cell had a more darkly stained cytoplasm with numerous of cell organelles. In the host cells attacked by the hyphal cells the limiting membranes of plastids were broken down and several vesicles were arrayed near the cell walls. No plasmodesmatal connections between the host and parasite cell walls were found; however, half-plasmodesmata were observed frequently on the side of the hyphal cell walls. These results suggested that the compatibility response in the self-parasitism of Cuscuta was expressed by cell walls, not by plasmodesmata, between the host and the parasite cells.

  • PDF

PFCB (Perfluorocyclobutane) Group을 포함한 랜덤 공중합체 고분자 전해질 막 제조 및 특성연구 (Preparation and Characterization of Random Copolymer Electrolyte Membranes Containing PFCB (Perfluorocyclobutane) Group)

  • 김정훈;김동진;장봉준;이수복;주혁종
    • 멤브레인
    • /
    • 제16권3호
    • /
    • pp.221-229
    • /
    • 2006
  • 본 연구는 불소관능기인 perfluorocyclobutane (PFCB), fluorenyl, sulfonyl계 방향족 화합물을 동시에 포함하는 술폰화된 랜덤 고분자 전해질 막의 제조 및 그 특성에 관한 것이다. 이러한 고분자 전해질 막은 세단계의 합성, 즉 trifluorovinyloxy그룹을 양말단에 포함하는 단량체의 합성, 중부가반응 형태의 열중합, 그리고 chlorosulfonic acid를 이용한 후술폰화를 통하여 얻어졌다. 후술폰화 반응은 고분자 내에 포함된 fluorenyl기의 함량에 따라 일정한 몰비의 술폰화제 비율로 고정하여 진행되었으며, 이에 따라 다양한 이온교환 능력(IEC)을 가지는 고분자를 쉽게 합성할 수 있었다. 제조된 단량체 및 고분자들의 구조와 순도는 각각 FT-IR과 NMR 그리고 질량분석기를 통하여 확인되었다. 술폰화된 fluorenyl기가 많아질수록 술폰화도와 이온교환 능력이 증가하는 것을 확인할 수 있었고 그에 따른 함수율도 역시 증가하는 거동을 보였다. 술폰화된 고분자들의 이온전도도를 측정한 결과 술폰화도가 증가할수록 이온 전도도가 증가하는 것을 관찰할 수 있었다, 이렇게 제조된 전해질막 중 S-1과 S-2의 경우 다양한 온도범위($25{\sim}80^{\circ}C$)에서 상용 전해질막인 Nafion-115를 능가하는 우수한 이온전도도를 나타냈다.