• 멤브레인
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• 제17권4호
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• pp.311-317
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• 2007

Poly(vinyl alcohol-co-ethylene) (PVA-co-PE)와 poly(styrene sulfonic acid-co-maleic acid) (PSSA-co-PMA)을 고분자 블렌딩 방법으로 50 : 50의 무게비율로써 수소이온 전도성 가교형 전해질막을 제조하였다. PSSA와 PMA이 3 : 1과 1 : 1의 몰 구성비로 되이 있는 두 가지 종류의 PSSA-co-PMA 고분자를 수소이온 전도성 고분자로 사용하였으며, PVA-co-PE 고분자는 에틸렌의 함량이 0, 27 그리고 44 mol%인 고분자를 사용하였다. 전해질 막은 PVA의 히드록실 그룹과 PMA의 카르복시릭 그룹 사이의 에스테르화 반응을 통한 열가교를 통해 제조하였고, FT-IR을 통하여 이를 확인하였다. PSSA-co-PMA의 몰비율이 3 : 1로 구성되어 제조된 전해질막은 몰비율 1 : 1로 구성되어 제조된 막보다 더 낮은 이온교환용량과 더 높은 함수율, 수소이온 전도도를 나타내었다. 또한, 전해질막에서 PE의 함량이 증가할수록 이온교환용량, 함수율, 수소이온 전도도가 계속해서 감소하는 경향성을 보였다. 전해질막의 이러한 물성들은 술폰산기의 함량과 친수성, 막의 가교구조 사이의 경쟁적인 효과로써 설명하였다.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2004년도 하계학술대회 논문집 C
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• pp.1661-1663
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• 2004

The effect of the triblock copolymer poly[styrene-b-(ethylene-co-butylene)-b-styrene](SEBS) on the formation of space charge of immiscible low density polyethylene/polystyrene(LDPE/PS) blends was investigated. The amount of charge accumulated in the 70/30(wt%) LDPE/PS blends decreased when the SEBS content increased up to 10 wt%. For compatibilzed and uncompatibilized blend, morphological observation showed that the addition of SEBS results in the domain size reduction of the dispersed PS phase and a better interfacial adhesion between LDPE and PS phases. The location of SEBS at a domain interface enables charges to migrate from one phase to the other via domain interface and therefore, results in a significant decrease in the amount of space charge for the LDPE/PS blends with SEBS.

• Bulletin of the Korean Chemical Society
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• 제31권5호
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• pp.1345-1348
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• 2010

Highly monodisperse polystyrene (PS) nanospheres were fabricated by surfactant-free emulsion polymerization in water using styrene, 2,2'-azobis(2-methyl propionamidine) dihydrochloride (AIBA), and poly(vinyl pyrrolidone) (PVP). The size and distribution of the PS nanospheres were systematically investigated in terms of initiator concentration, stabilizer concentration, reaction temperature, reaction time, and reactant concentration. With increasing AIBA initiator concentration, PS particle sizes are raised proportionally, and can be controlled from 120 to 380 nm. Particle sizes were reduced with increasing PVP concentration. This decrease occurs because a high PVP concentration leads to a large number of primary nuclei in the early stage of polymerization. When the reaction temperature increased, the sizes of the PS particles decrease slightly. The particles grew quickly during the initial reaction stage (1-3 h) and the growth rate became steady-state after 6 h. The PS sizes approximately doubled when the reactant (styrene, PVP, azo-initiator) concentrations were increased by a factor of eight.

• Bulletin of the Korean Chemical Society
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• 제33권9호
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• pp.2966-2970
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• 2012

Fullerene/polystyrene ($C_{60}$/PS) nano particle was prepared by using emulsion polymerization. Styrene and fullerene were emulsified in aqueous media in the presence of poly(N-vinyl pyridine) as an emulsion stabilizer, and polymerization was initiated by water soluble radical initiator, potassium persulfate. The obtained nano particles have an average diameter in the range of 400-500 nm. The fullerene contents in the nano particle can be controlled up to 15 wt % by varying the feed ratio, which was confirmed by themogravimetric analysis (TGA) and elemental analysis (EA). The structure and morphologies of the $C_{60}$/PS nano particles were examined by various analytical techniques such as dynamic light scattering (DLS), scanning electron microscope (SEM), transmission electron microscope (TEM), electron diffraction (ED) pattern, X-ray powder diffraction (XRD), and UV spectroscopy. Unlike conventional $C_{60}$/PS particles initiated by organic free radical initiators, in which the fullerene is copolymerized forming a covalent bond with styrene monomer, the prepared $C_{60}$/PS nano particles contain pristine fullerene as secondary particles homogeneously distributed in the polystyrene matrix.

• Macromolecular Research
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• 제14권2호
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• pp.194-198
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• 2006

Polystyrene, PS, particles of 450 nm diameter and poly(styrene-co-styrene sulfonate), PSS, particles of 140-160 nm diameter were prepared by emulsifier-free emulsion polymerization. The surfaces of the PS and PSS particles were coated with Ag nanoparticles for the application of antimicrobial agents by reduction of Ag ions using ${\gamma}$-irradiation. The Ag-PS and Ag-PSS were characterized by High-Resolution Transmittance Electron Microscopy (HR-TEM), Field-Emission Scanning Electron Microscopy (FE-SEM), and Energy Dispersive X-ray Spectroscopy (EDXS). The HR-TEM and EDXS data showed that the Ag nanoparticles were loaded on the surface of the PS and PSS particles, respectively. The antimicrobial efficiency of the Ag-PS and Ag-PSS particles (0.4 g) with ca. 100 ppm Ag, which was coated onto yam (KS K 0905-1996 rule), was tested against Staphylococcus aureus ATCC 6538 and Klebsiella pneumoniae ATCC 4352 after 100 washing cycles (KS K 0432-1999 rule). The antimicrobial efficiency of the Ag-PS particles against Staphylococcus aureus ATCC 6538 and Klebsiella pneumoniae ATCC 4352 was 99.9% after 100 cycles washing., confirming that the Ag-PS particles can be used as antimicrobial agents.

• 폴리머
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• 제34권2호
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• pp.126-132
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• 2010

메탄올 용매에서 고분자 촉진 단량체와 소디윰 스티렌 슐포네이트를 방사선 그래프트 방법으로 양이온 교환 PVdF 맴브레인을 제조하였다. 고분자 촉진 단량체로서 스티렌, 아크릴산, 비닐 피롤리돈을 사용하였다. 또한, 음이온 교환 PVdF 맴브레인도 방사선 그래프트 중합법에 의해 제조하였다. 양이온 및 음이온 교환 PVdF 맴브레인은 SEM, XPS 그리고 열분석기기를 통해 특성평가를 하였고 성공적으로 합성됨을 확인할 수 있었다. 그래프트 수율, 이온교환기의 양 및 침투율은 각각 30.0~32.3%, 2.81~3.01 mmol/g 그리고 66.6~147%로 평가되었으며, 20 $^{\circ}C$에서 이온 전도도를 측정한 결과 0.020~0.053 S/cm 이었다. 최종적으로, 제조된 양이온 및 음이온교환 PVdF 맴브레인은 전지격막으로서 충분히 사용될 수 있음을 확인할 수 있었다.

• 폴리머
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• 제30권5호
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• pp.437-444
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• 2006

Hydroxypropyl methylcellulose phthalate (HPMCP)에 isophorone diisocyanate (IPDI)와 2-hydroxyethyl methacrylate (HEMA)를 순차적으로 반응하여 우레탄 그룹을 형성하고 HPMCP에 비닐 그룹을 도입하여 반응형(reactive) HPMCP를 합성하였다. 제조된 반응형의 HPMCP와 반응전의 순수한 HPMCP의 분자량, 산가, 임계 미셀 농도(CMC) 등을 측정하였으며, 스티렌의 유화 중합에 고분자 유화제로서 도입하였다. HPMCP의 함량을 단량체인 스티렌 대비로 6, 9, 12, 18, 24 wt%로 도입하여 HPMCP 혼성 폴리스티렌 나노입자를 제조하고, 최대 중합 속도($R_{p,max}$), 입자당 평균라디칼 개수(n), 입자 크기 분포 등을 분석하였다. 또한 제조된 HPMCP 혼성 폴리스티렌 나노입자의 모폴로지를 TEM으로 분석하여 core-shell 구조임을 확인하였으며, TGA를 이용하여 열적안정성의 변화를 분석하였다. 반응형 HPMCP는 순수 HPMCP와는 달리 HEMA의 비닐 그룹으로 인해 높은 중합속도와 작은 입자 크기, 높은 표 값을 나타내었으며, 높은 젤 함량을 나타내었다.

• 멤브레인
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• 제24권6호
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• pp.463-471
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• 2014

폴리스티렌계 음이온교환막은 제조가 쉽고 공정이 간단한 장점을 갖고 있으나 막의 취성이 높아 내구성이 떨어지는 단점을 가지고 있다. 이를 보완하여 유연하고 우수한 내구성을 갖는 막을 만들기 위해 acrylonitrile-butadiene rubber를 첨가제로 사용하여 음이온교환막을 제조하였다. 다양한 조성의 vinylbenzylchloride와 styrene, divinylbenzene, acrylonitrile-butadiene rubber 그리고 benzoyl peroxide로 이루어진 단량체 용액을 지지체인 직물 형태의 지지체인 poly(propylene)위에 캐스팅 후 열중합 가교시킨 다음 trimethylamine과 acetone을 이용하여 음이온 교환기($-N+(CH_3)_3$)를 함유하는 복합막을 제조하였다. 음이온 교환막 제조시 첨가제의 함량에 따른 막의 성능을 평가하여 최적화 비율을 찾고, 단량체의 함량을 변화하여 함수율, 이온교환용량(IEC) 및 전기저항 값을 측정하였다. 그 결과 최적화 비율로 제조된 막들은 아스톰사의 상용화 음이온 교환막(AMX)보다 높은 IEC와 낮은 전기저항 값을 나타내는 동시에 유연성과 내구성이 우수한 막이 만들어진 것을 확인할 수 있었다.

• 펄프종이기술
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• 제44권5호
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• pp.21-31
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• 2012

In this study, we modified the surface of ground calcium carbonate (GCC) with polyelectrolytes with different molecular weight using Layer-by-Layer (LbL) multilayering technique and investigated its effect on the paper properties. Polydiallydimethylammonium chloride (poly-DADMAC) and poly sodium 4-styrene sulfonate (PSS) which have different molecular weights were used for LbL multilayering. Zeta potential and particle size of the LbL modified GCC were measured. After preparation of handsheets, their structural and mechanical properties were evaluated. The zeta potential and average particle size of the modified GCC were affected by the molecular weight of anionic polyelectrolyte (PSS). The zeta potential was higher and the particle size was smaller when GCC was treated by PSS with high molecular weight compared to the case with low molecular weight of PSS. The tensile and internal bond strength of the handsheets was increased with an increase in the number of layers on GCC particles, but the molecular weight of polyelectrolyte did not significantly affect the paper strength.

• 반도체디스플레이기술학회지
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• 제7권2호
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• pp.49-53
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• 2008

The yellow base polymer light emitting diodes(PLEDs) with double emission and hole blocking layers were prepared to improve the light efficiency. ITO(indium tin oxide) and PEDOT : PSS[poly(3,4-ethylenedioxythiophene) : poly(styrene sulfolnate)] were used as cathode and hole transport materials. The PFO[poly(9,9-dioctylfluorene)] and MEH-PPV[poly(2-methoxy-5(2-ethylhe xoxy)-1,4-phenylenevinyle)] were used as the light emitting host and guest materials, respectively. TPBI[Tpbi1,3,5-tris(N-phenylbenzimidazol-2-yl)benzene] was used as hole blocking layer. To investigate the optimization of device structure, we prepared four kinds of PLED devices with different structures such as single emission layer(PFO : MEH-PPV), two double emission layer(PFO/PFO : MEH-PPV, PFO : MEH-PPV/PFO) and double emission layer with hole blocking layer(PFO/PFO : MEH-PPV/TPBI). The electrical and optical properties of prepared devices were compared. The prepared PLED showed yellow emission color with CIE color coordinates of x = 0.48, y = 0.48 at the applied voltage of 14V. The maximum luminance and current density were found to be about 3920 cd/$m^2$ and 130 mA/$cm^2$ at 14V, respectively for the PLED device with the structure of ITO/PEDOT : PSS/PFO/PFO : MEH-PPV/TPBI/LiF/Al.