• Title/Summary/Keyword: Functional polymer

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Synthesis of Poly(2,6-dimethyl-1,4-phenylene oxide) containing Poly(styrene sulfonic acid) for Fuel Cell (연료전지용 Poly(styrene sulfonic acid)를 갖는 Poly(2,6-dimethyl-1,4-phenylene oxid)의 합성)

  • An, Sung-Guk;Cho, Chang-Gi
    • Proceedings of the Korean Fiber Society Conference
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    • 2003.10b
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    • pp.34-37
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    • 2003
  • The development and improvement of advanced fuel cell systems is a major topic of current research, since fuel cells are considerably more efficient than other energy converters$^1$. In proton exchange membrane fuel cell and direct methanol fuel cell the polymer membrane represents a key component. The membrane materials fulfill complex requirements. It has to combine electrochemical stability, workability, high ionic conductivity, low permeation of the reactants (methanol etc.) (omitted)

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Thermally Induced Mesophase Development in Ethanesilica Films via Macromolecular Templating Approach

  • Cho, Whirang;Char, Kook-Heon;Kwon, Su-Yong
    • Macromolecular Research
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    • v.17 no.9
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    • pp.697-702
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    • 2009
  • Mesoporous ethanesilica thin film was prepared using PEO-PLGA-PEO triblock copolymers as structure-directing agents and (1,2-bis(triethoxysilyl) ethane BTESE; bridged organosilicates) as inorganic precursors via one-step sol-gel condensation of ethanesilica precursors. The mesostructure of ethanesilica films is critically dependent on the processing experimental parameters after the hydrolyzed silica sol mixture was spin-cast. This study examined the effects of the block copolymer template/organosilica precursor ratio in the casting solution and aging period before calcination of the mesostructure. It was further demonstrated that mesoscopic ordering of organosilicate thin films is induced by the rearrangement of block copolymer template/organosilica hybrid during thermal decomposition of the PEO-PLGA-PEO triblock copolymer. The mesoporous structure and morphology were characterized by SAXS, TEM and solid-state NMR measurement.

Spherulitic Morphologies of Poly(ethylene terephthalate), Poly(ethylene 2,6-naphthalate), and Their Blend

  • Lee, Jong-Kwan;Lee, Kwang-Hee;Jin, Byung-Suk
    • Macromolecular Research
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    • v.10 no.1
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    • pp.44-48
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    • 2002
  • The supermolecular structures of poly(ethylene terephthalate) (PET), poly(ethylene 2,6-naphthalate) (PEN), and their blend were investigated with optical microscopy and small angle light scattering. With increasing the crystallization temperature, incomplete spherulitic texture was developed for the PET samples. At a high crystallization temperature of 220 $^{\circ}C$, the light scattering pattern represented a random collection of uncorrelated lamellae. The general morphological appearances for the PEN samples were similar to that of the PET. A notable feature was that the spherulites of the PEN formed at 200 $^{\circ}C$ showed regular concentric bands arising from a regular twist in the radiating lamellae. The spherulitic morphology of the PET/PEN blend was largely influenced by the changes of the sequence distribution in polymer chains determined by the level of transesterifcation. The increased sequential irregularity in the polymer chains via transesterification caused a morphological transition from a regular folded crystallite to a tilted lamellar crystallite.

Thermoresponsive Phase Transitions of PLA-block-PEO-block-PLA Triblock Stereo-Copolymers in Aqueous Solution

  • Lee, Hyung-Tak;Lee, Doo-Sung
    • Macromolecular Research
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    • v.10 no.6
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    • pp.359-364
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    • 2002
  • A series of PLA-PEO-PLA triblock stereo-copolymers with varying PLA/PEO and L-DL-LA ratios were synthesized via ring opening pelymerizations. Aqueous solutions of these copolymers undergo thermo-responsive phase transitions as the temperature monotonically increases. Further study shows that there is a critical gel concentration (CGC), and also lower and upper critical gel temperatures (CGTs), at which the thermo-responsive phase transition occurs. The CGC and CGTs are affected by various factors such as block length, as well as the compositions of the PLA blocks and of the additives. In particular, the changes in the phase diagram produced by varying the L-/DL-LA ratio in the PLA blocks were determined to be mainly due to consequent stereo-regularity changes in the PLA blocks.

Porosity of Polymer-Modified Mortars Using Methylmethacrylate-Butyl Acrylate Latexes with Various Monomer Ratios (MMA/BA 합성 라텍스 혼입 폴리머 시멘트 모르타르의 세공성상)

  • 형원길;송해룡;김완기;소양섭
    • Proceedings of the Korea Concrete Institute Conference
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    • 2002.05a
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    • pp.87-92
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    • 2002
  • At present, the polymer-modified mortars are used as high-performance as well as multi-functional materials in the construction industry. The purpose of this study is to synthesize polymer to modify in cement mortars and make test samples to understand pore size distribution. This paper deals with the effect of monomer ratio on the typical properties of polymer-modified mortars using Methylmethacrylate-Butyl Acrylate(MMA/BA) latexes synthesized through emulsion polymerization. From the results, we knew that the pore volume of polymer-modified mortars using Methylmethacrylate-Butyl Acrylate latexes at bound MMA contents of 70 and 60 percent is 7.5-75cm$^3$/g and the fine pore volume is increased with an increase in the polymer-cement ratio. The total pore volume of polymer-modified mortars using MMA/BA latexes is linearly reduced with an increase in the bound MMA content and increased in the polymer-cement ratio.

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Adsorption of Aromatic Compounds on a QCM System Coated with Polymer Films (고분자 필름이 코팅된 QCM 시스템에 의한 방향족 화합물의 흡착)

  • Hwang, Min-Jin;Shim, Wang-Geun;Moon, Hee
    • Korean Chemical Engineering Research
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    • v.51 no.2
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    • pp.233-239
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    • 2013
  • A quartz crystal microbalance (QCM) system coated with poly (isobutylene), polystyrene, and poly (methyl methacrylate) has been prepared to measure the adsorption amounts of benzene, toluene, and p-xylene at very low pressures. The resonant frequency shift of the QCM system is proportional to the increase in pressure in all experiments. The Henry's constants for all adsorbates on the polymer films are obtained from experimental data and compared with the minimum adsorption potential energies between adsorbates and the polymer films. In general, there is an explicit correlation between adsorption amount and the minimum adsorption potential energy.

Synthesis of Molecularly Imprinted Polymers for Chiral (S)-Ibuprofen and Their Molecular Recognition Mechanism (키랄(S)-이부푸로펜 함유 고분자의 합성과 제조된 고분자의 분자 인식 메카니즘)

  • Huangfu, Fengyun;Wang, Bing;Sun, Yan
    • Polymer(Korea)
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    • v.37 no.3
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    • pp.288-293
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    • 2013
  • A group of molecularly imprinted polymers (MIPs) with specific recognition for chiral (S)-ibuprofen were successfully prepared based on hydrogen bonds, utilizing ${\alpha}$-methacrylic acid as a functional monomer. The IR analysis of MIPs showed that the blue- and red-shifted hydrogen bonds were formed between templates and functional monomers in the process of self-assembly imprinting and re-recognition, respectively. According to UV-Vis analysis, we found that the ratio of host-guest complexes between template molecule and functional monomer was 1:1. The effect of cross-linker's quantity on the polymerization was studied by transmission electron microscope (TEM). The adsorption selectivity experiments indicated that MIPs exhibited higher selectivity to (S)-ibuprofen than those to ketoprofen and (R)-ibuprofen, (S)-ibuprofen's structural analogs.

The Effect of Ions on Thermal Behaviors of Water in Poly(acrylic acid)/Water Mixtures (폴리아크릴산/$H_2O$ 혼합물에서 $H_2O$ 열적 거동에 미치는 이온의 영향)

  • Guan, Lan;Xu, Hongyan;Huang, Dinghai
    • Polymer(Korea)
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    • v.34 no.4
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    • pp.386-389
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    • 2010
  • Thermal behaviors of water in the poly(acrylic acid) (PAA)/water mixtures with 0.1 M NaCl, HCl, and NaOH were investigated by DSC. It showed that adding ions in the mixtures affected the crystallization of water evidently. Compared with the PAA/water mixtures, the $T_m$ of freezable bound water in the mixtures with ions moved to lower values and varied with different cations and anions, due to the stabilization or destabilization of the hydrogen-bonding hydration between polymers and water molecules through ionic hydration. The content of non-freezable bound water in the non-crystalline phase of the PAA/water mixtures with ions was not constant, it increased with total water content gradually, owing to the more binding sites created by ions. The ions could change the distribution of different states of water in the polymer aqueous solutions evidently.

Functional Polymeric Materials for Biomedical Application (생체의료용 기능성 고분자 재료의 개발)

  • Sung, Yong-Kiel;Song, Dae-Kyung;Sung, Jung-Suk
    • Polymer(Korea)
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    • v.30 no.1
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    • pp.1-9
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    • 2006
  • The development of functional polymeric materials for biomedical application has progressed on the basis of functionality, biocompatibility and biodegradability. In this paper we review the functional polymeric biomaterialsbased systems and propose a range of biomedical applications in the near future. These systems include the functional biodegradable polymers synthesized in our research laboratory, biodegradable polymeric materials, thermosensitive polymeric materials, cationic polymeric materials, non-condensing polymeric biomaterials, bio-polymeric DNA matrix for tissue engineering, and polymeric biomaterials for RNA interference (RNAi) technology.