• 폴리머
• /
• 제35권2호
• /
• pp.130-135
• /
• 2011

전자 기기의 빠른 발전에 따른 무선 기기들의 사용은 급격히 늘어나고 있다. 그래서 이런 제품에 자가 발전이 가능한 재료를 적용시키는 사례가 점차 늘고 있다. 여기에 사용되는 재료로서 poly(vinylidene fluoride) (PVDF)가 있는데 PVDF는 piezoelectricity를 낼 수 있는 특별한 결정구조인 ${\beta}$-phase를 가지고 있다. 이 논문에서는 piezoelectricity에 결정적인 영향인 ${\beta}$-phase 함량을 증가시키기 위해 다층 PVDF 필름을 제조하였다. 이 PVDF 필름은 용매인 DMAc에 10%로 용해시킨 깃으로 spin rate는 850 rpm, spin time은 60초이며 건조온도는 $60^{\circ}C$이다. 비교적으로 다층 필름은 단열 층보다 더 높은 ${\beta}$-phase함량을 나타내었다 이 ${\beta}$-phase함량은 4-layer 필름이 되기까지 점차 증가되었으며 최대 함량은 7.72이다.

• 폴리머
• /
• 제25권3호
• /
• pp.367-374
• /
• 2001

여러 가지 탄소함유가스로부터 Ni 및 Ni-Cu의 합금촉매를 사용하는 화학증착반응에 의해 제조한 나노탄소섬유를 충전재로 하고, poly(vinylidene fluoride) (PVDF)를 매트릭스로 이용하여 복합재를 제조하여 전자파 차폐성능을 조사해보았다. 전자파 차폐용 충전재의 중요한 물성치인 나노탄소섬유의 전기전도도는 10000psi 압력에서 4.2∼22.4S/cm 사이에 분포하였다. 나노탄소섬유/PVDF 복합재의 전기전도도는 0.22∼2.46 S/cm 사이에 값을 보였고, 전자파 차폐성능은 2∼13 dB 범위를 나타내었다. 나노탄소섬유의 전기전도도는 열처리 온도와 시간의 증가에 따라 높아지지만, 얻어지는 복합재의 전기전도도는 초기에 급속한 증가 후 일정해지는 경향을 나타내었다. 복합재의 전자파 차폐성능은 열처리 온도와 시간의 증가에 따라 증가하다가 감소하였고, 복합재의 전기전도도에 비례하였다. 열처리가 진행됨에 따라 나노탄소섬유의 비표면적이 감소하였으며, 전자파 차폐성능에 충전재의 전기전도도 외에 비표면적이 중요한 변수임을 알 수 있었다.

• 한국재료학회지
• /
• 제33권12호
• /
• pp.517-524
• /
• 2023

BaTiO₃-Poly vinylidene fluoride (PVDF) solution was prepared by adding 0~25 wt% BaTiO₃ nanopowder and 10 wt% PVDF powder in solvent. BaTiO₃-PVDF film was fabricated by spreading the solution on a glass with a doctor blade. The output performance increased with increasing BaTiO₃ concentration. When the BaTiO₃ concentration was 20 wt%, the output voltage and current were 4.98 V and 1.03 ㎂ at an applied force of 100 N. However, they decreased when the over 20 wt% BaTiO₃ powder was added, due to the aggregation of particles. To enhance the output performance, the generator was poled with an electric field of 150~250 kV/cm at 100 ℃ for 12 h. The output performance increased with increasing electric field. The output voltage and current were 7.87 V and 2.5 ㎂ when poled with a 200 kV/cm electric field. This result seems likely to be caused by the c-axis alignment of the BaTiO₃ after poling treatment. XRD patterns of the poled BaTiO₃-PVDF films showed that the intensity of the (002) peak increased under high electric field. However, when the generator was poled with 250 kV/cm, the output performance of the generator degraded due to breakdown of the BaTiO₃-PVDF film. When the generator was matched with 800 Ω resistance, the power density of the generator reached 1.74 mW/m². The generator was able to charge a 10 ㎌ capacitor up to 1.11 V and turn on 10 red LEDs.

• Macromolecular Research
• /
• 제17권10호
• /
• pp.757-762
• /
• 2009

The micro domain structures and crystallization behavior of the binary blends of poly(methyl methacrylate)-b-poly(pentafluorostyrene)-b-poly(methyl methacrylate) (PMMA-PPFS-PMMA) triblock copolymer with a low molecular weight poly(vinylidene fluoride) (PVDF) were investigated by small-angle X-ray scattering (SAXS), small-angle light scattering (SALS), transmission electron microscopy (TEM), optical microscopy, and differential scanning calorimetry (DSC). A symmetric, PMMA-PPFS-PMMA triblock copolymer with a PPFS weight fraction of 33% was blended with PVDF in N,N-dimethylacetamide (DMAc). In the wide range of PVDF concentration between 10.0 and 30.0 wt%, PVDF was completely incorporated within the PMMA micro domains of PMMA-PPFS-PMMA without further phase separation on a micrometer scale. The addition of PVDF altered the phase morphology of PMMA-PPFS-PMMA from well-defined lamellar to disordered. The crystallization of PVDF significantly disturbed the domain structure of PMMA-PPFS-PMMA in the blends, resulting in a poorly-ordered morphology. PVDF displayed unique crystallization behavior as a result of the space constraints imposed by the domain structure of PMMA-PPFS-PMMA. The pre-existing microdomain structures restricted the lamellar orientation and favored a random arrangement of lamellar crystallites.

• Korea-Australia Rheology Journal
• /
• 제20권4호
• /
• pp.213-220
• /
• 2008

The effects of temperature on the rheological properties of the solutions of poly(vinylidene fluoride-co-hexafluopropylene) (PVDF-HFP) in dimethyl acetamide (DMAc) were investigated in terms of frequency and concentration. The effects of temperature on the intrinsic viscosity of the solutions were discussed. In dynamic rheological measurement, the concentrated solutions showed a little unexpected rheological response; as temperature was increased dynamic viscosity was increased and the solutions exhibited more noticeable Bingham body character over the temperature range, 30 to $70^{\circ}C$. In addition, the solution gave longer relaxation time, lower value of loss tangent and higher value of yield stress at higher temperature and at higher concentration. On the other hand, the dilute solutions revealed that intrinsic viscosity was decreased and its Huggins constant was increased with increasing temperature. These physical parameters suggested that the increase of viscosity with increasing temperature resulted from the localized gelation of PVDF-HFP due to reduced solubility to the solvent.

• Journal of Electrical Engineering and Technology
• /
• 제13권4호
• /
• pp.1692-1696
• /
• 2018

Ferroelectric $BaTiO_3$/poly(vinylidene fluoride) (PVDF) nanocomposite films were successfully prepared by mixing $BaTiO_3$ nano-particles into PVDF solution dissolved in dimethylformamide under ultrasonification. The mixture was casted onto glass petri dish and then annealed at $100^{\circ}C$ for 12 h in vacuum dry oven. Crystal structure and surface morphology of the samples were analyzed by using an X-ray diffraction analysis and a field emission-scanning electron microscope, respectively. The relative dielectric permittivity and loss tangent were determined in the frequency range of 50 Hz to 1 MHz. For the $BaTiO_3/PVDF$ nanocomposites, the entire diffraction peaks match those indicated by standard $BaTiO_3$ perovskite structure. The FE-SEM image reveals the homogeneity of the $BaTiO_3$ nanopowder distribution and also predominant 0-3 connectivity. All results show that the dielectric properties of the nanocomposite films are desirable and the fabrication technique for preparing the $BaTiO_3/PVDF$ nanocomposites has a potential in the electronic applications.

• 멤브레인
• /
• 제20권4호
• /
• pp.320-325
• /
• 2010

화학적 안정성이 양호하고, 제막조건이 온화한 재료인 poly(vinylidene fluoride) (PVDF)를 주재료로 사용하여 용매, 첨가제, 혼합고분자 및 제막조건의 변화에 따른 고강도 친수성 정밀여파(microfiltration, MF) 중공사 분리막의 실험에 의해 고찰하였다. 제조된 MF 중공사막의 막성능은 평균 공경 $0.3{\mu}m$, 인장강도 $42kg_f/cm^2$, 순수 투과유량은 600 LMH을 얻었다. 제막과정에서 다양한 첨가제의 막성능을 검토한 결과는 순수투과유량과 제거율에 상당한 영향을 미치고 있음을 알 수 있었다. MF막의 친수성을 개선하기 위해 소수성 PVDF와 상호 용해성 이 좋은 친수성 poly(methyl methacrylate) (PMMA)를 혼합하여 투과성능과 제거율을 개선한 우수한 친수성 MF막을 제조할 수 있었다.

• 한국섬유공학회:학술대회논문집
• /
• 한국섬유공학회 2001년도 가을 학술발표회 논문집
• /
• pp.271-274
• /
• 2001

최근 압전성 및 유전성, 비선형 광학전도성 등과 같은 특성을 갖는 전기전자 및 광기능성 고분자에 대한 연구가 많이 이루어지고 있다[1-2]. 그 중에서 압전 및 초전성을 나타내는 대표적 유기 고분자인 poly(vinylidene fluoride)(PVDF)의 경우 압전성을 향상시키기 위하여 vinylidene. fluoride(VDF)나 vinyl fluoride(VF), trifluoroethylene(TrFE) 등과 공중합시킨 고분자들에 대한 연구가 활발히 진행되어 왔다[3-4]. (중략)

• 폴리머
• /
• 제28권6호
• /
• pp.509-518
• /
• 2004

비대칭 블록 공중합체와 단일고분자로 구성된 블렌드의 미세 도메인 구조와 결정화 거동을 소각 X-선 산란, 광학 현미경 및 DSC를 사용하여 조사하였다. 본 연구에서는 폴리(메틸 메타크릴레이트) 블록의 무게 분률이 0.53인 폴리(메틸 메타크릴레이트)-폴리스티렌 이종 블록 공중합체 (PMMA-b-PS)를 저분자량 폴리(비닐리덴 플루오라이드) (PVDF)와 혼합하였다. PVDF 함량 증가에 따라 블렌드 미세구조가 라멜라에서 실린더 구조로 전이하였으며, PVDF의 결정화는 결정화 이전에 형성된 미세구조의 배열을 교란시켜 질서도가 낮은 형태를 야기시켰다. 또한, PVDF 결정화 거동은 PMMA 블록과의 혼화성 및 미세 도메인에 의해 부가되는 공간적 제한에 큰 영향을 받았다.

• Korean Membrane Journal
• /
• 제9권1호
• /
• pp.57-63
• /
• 2007

Amphiphilic graft copolymer from poly(vinylidene fluoride) (PVDF) was synthesized using atom transfer radical polymerization (ATRP) for composite nanofiltration membranes. Direct initiation of the secondary fluorinated site of PVDF facilitates grafting of tert-butyl methacrylate (tBMA). Amphiphilic PVDF-g-PMAA graft copolymer with a 51:49 wt ratio was obtained by hydrolyzing poly(tert-butyl methacrylate) (PtBMA) to poly(methacrylic acid) (PMAA). Wide angle X-ray scattering (WAXS) and differential scanning calorimetry (DSC) confirmed the decrease of crystallinity of PVDF upon graft copolymerization. Composite nanofiltration membranes were prepared from PVDF-g-PMAA as a top layer coated onto PVDF ultrafiltration (UF) support membrane. The morphology and hydrophilicity of membranes were characterized using scanning electron microscopy (SEM) and contact angle measurement. The rejections of composite membranes were 80.2% for $Na_2SO_4$ and 28.4% for NaCl, and the solution flux were 9.5 and $14.5\;L/m^2\;h$ at 1.0 MPa pressure.