• The Korean Journal of Ceramics
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• 제2권3호
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• pp.152-156
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• 1996

Fine (~0.09 $\mu$m) $\beta$-SiC Powders with 3.3wt% of large (~0.44$\mu$m) $\alpha$-SiC of $\beta$-SiC particles (seeds) added were hotpressed at 175$0^{\circ}C$ using $Y_2O_3$, $Al_2O_3$ and CaO as sintering aids and then annealed at 185$0^{\circ}C$ for 4 h to enhance grain growth. The resultant microstructure and polytypes were analyzed by high resolution electron microscopy (HREM).Growth of $\beta$-SiC with high density of microtwins and formation of ${\alpha}/{\beta}$ composite grains consisting of $\alpha$-SiC domain sandwiched between $\beta$-SiC domains were found in both specimens. When large $\alpha$-SiC (mostly 6H) seeds were added, the $\beta$-SiC transformend preferentially to the 6H polytype. In contrast, when large $\beta$-SiC (3C) seeds were added, the fine $\beta$-SiC transformed preferentially to the 4H polytype. Such results suggested that the polytype formation in SiC was influenced by crystalline form of seeds added as well as the chemistry of sintering aids. The ${\alpha}/{\beta}$ interface played and important role in the formation of elongated grains as evidenced by presence of ${\alpha}/{\beta}$ composite grains with high aspect ratio.

• 대한전기학회논문지:전기물성ㆍ응용부문C
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• 제50권10호
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• pp.479-488
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• 2001

The effects of accelerated Ultraviolet (UV) radiation on High temperature vulcanized (HTV), Room temperature vulcanized (RTV) silicone rubber and two types of ethylene propylene diene terpolymer (EPDM) used for composite insulator were inverstigated by hydrophobicity class (HC), surface voltage decay after corona charging, SEM-EDS, FTIR and XPS. The contact angle in two kinds of silicone rubber was scarcely change, but EPDM occurred to the loss of hydrophobicity followed by surface cracking and chalking. The surface voltage decay on UV-treated silicone rubber and EPDM showed a different decay trend with UV treatment. EDS and XPS analysis indicated that the oxygen content increased with UV treatment time in all samples. For silicone rubber, the oxidized groups of inorganic silica-like structure increased with UV treatment time. The oxidized carbon of C=0, O=C-O in EPDM increased. These oxidized surface for each material had different electrostatic characteristics, so deposited charges were expected to have different impacts on their surface hydrophobicity. The degradation mechanism based on our results was discussed.

• 한국조명전기설비학회지:조명전기설비
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• 제7권2호
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• pp.51-56
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• 1993

Epoxy 복합재료의 충전제 및 수분함유의 유전특성에 대한 영향을 고찰한 결과를 요약하면 다음과 같다. 1) ${\varepsilon}_\tau$의 주파수 의존성은 시편1과 시편2의 경우에서 $140^{\circ}C$이하에서 직선적인 특성을 나타내고 있으며 수분의 함유시에도 직선적인 변화를 하고 있으므로 주파수나 습도 센서소자로서 개발이 가능하다. 2) 100[Hz]~3[kHz]의 범위에서 $tan{\delta}$ 주파수 의존성은 캐리어 이동에 의한 도전손실 보다 쌍극자완화에 의한 손실이 지배적이며 수분에 영향은 낮은 주파수에서 크게 받는다.

• 한국응용과학기술학회지
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• 제27권2호
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• pp.183-187
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• 2010

Core-Shell polymers of silicone dioxide-styrene system were prepared by sequential emulsion polymerization. In inorganic/organic Core-Shell composite particle polymerization, silicone dioxide adsorbed by surfactant sodium dioctyl sulfosuccinate (EU-DO133L) was prepared initially and then core silicone dioxide was encapsulated emulsion by sequential emulsion polymerization using styrene at the addition of potassium persulfate (KPS) as an initiator. We found that $SiO_2$ core shell of $SiO_2$/styrene structure was formed when polymerization of styrene was conducted on the surface of $SiO_2$ particles, and the concentration sodium dioctyl sulfosuccinate (EU-DO133L) was 0.5~2.0g. The structure of core-shell polymer were investigated by measuring to the thermal decomposition of polymer composite using thermogravimetric analyzer and morphology of latex by scanning electron microscope(SEM).

• 공업화학
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• 제20권5호
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• pp.527-531
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• 2009

전구체로서 bis(triethoxy silyl) benzene (BTEB), 구조유도체로서 dodecyl trimethyl ammonium bromide (DTMA)를 사용하여 periodic mesoporous organosilicas (PMO) 합성하였다. PMO를 XRD, TEM, 그리고 NMR로 확인한 결과 육각 벌집형태의 메조포러스한 물질임을 확인하였다. 합성한 PMO에 polyethylene oxide (PEO)를 삽입하여, DSC와 XRD로 확인한 결과 고분자가 PMO에 삽입되는 과정에서 고분자의 결정성 용융 온도가 감소하다가 결국 사라짐을 확인하였다. 이러한 결과는 고분자 사슬이 PMO의 기공에 삽입되었다는 것이며, 삽입된 고분자 사슬은 PMO의 골격구조에 의하여 제한 받아서 비결정성 형태의 구조를 지니고 있음을 보여주고 있다.

• 폴리머
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• 제30권2호
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• pp.135-139
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• 2006

인체 뼈의 주성분인 수산화인회석(hydroxyapatite, HAP)이 충전된 고분자 복합체를 제조하고 이들의 치과적 물성을 분석하여 치과용 수복재료로의 응용성을 확인하고자 하였다. 복합체 제조에 사용된 기질인 아크릴계 단량체는 가시광선으로 경화시켰다. 실험 결과, HAP는 무게비로 65%까지 첨가되었으며 중합깊이는 6.0 mm 정도로서 일반적 치과용 수복재료로의 응용이 가능함을 확인하였다. 제조된 고분자 복합체의 중합전환율은 HHP 첨가량이 늘어날수록 약간 감소하였으며 중합수축률은 HAP 변화량에의 의존성이 거의 없었다. 복합체의 기계적 물성은 HAP함량이 증가할수록 간접인장강도는 증가하였고 굴곡강도는 큰 변화가 없었다. 그러나 그 값들은 치의학에서 규정한 값들을 상회하여 치과용 재료로의 응용 가능성이 매우 높음을 확인할 수 있었다.

• 접착 및 계면
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• 제2권1호
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• pp.1-8
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• 2001

본 연구에서는 슬러지 및 폐타이어 칩(WTC)으로부터 얻은 폐석분을 충전제로 하고 불포화 폴리에스테르 수지(UPE)를 결합재로 하여 고분자 혼성복합재를 제조하였다. 또한 무기 충전제와 매트릭스 사이의 계면 결합뿐만 아니라 매트릭스 내의 충전제의 분산을 향상시키기 위하여 실란[${\gamma}$-methacryloxy propyl trimethoxy silane(${\gamma}$-MPS)]을 이용하여 표면처리를 하였다. 혼성복합재의 구조적 특성과 기계적 물성에 대한 이 무기 재활용 충전제의 함량과 농도의 영향은 Mercury Porosimeter 및 주사전자현미경을 이용하여 관찰하였다.

• Bulletin of the Korean Chemical Society
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• 제35권2호
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• pp.392-396
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• 2014

New organic-inorganic composite of 2,4-dihydroxybenzophenone (BP-1) encapsulation into dodecylbenzenesulfonate (DBS) modified layered double hydroxide (LDH) was successfully prepared. The surface, structural, thermal and absorption properties of the BP-1/DBS-LDH nanohybrid was characterized by BET analysis, scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TG) and diffuse reflectance UV-Vis absorbance spectra (DRUV-vis). The interlayer configuration of composite and the adsorption mechanism of BP-1 on MgAl-DBS-LDH were discussed. It was suspected that DBS anions located in the form of monolayer arrangement with a $75^{\circ}$ anti parallel angle between dodecylbenzenesulfonate chain axis. The diffuse reflectance UV-Vis absorbance results revealed that the UV absorbing wavelength of BP-1/DBS-LDH evidently extends to about 400 nm, which shows that the BP-1/DBS-LDH has the potential application as a UV absorber.

• Macromolecular Research
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• 제12권5호
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• pp.443-450
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• 2004

We have studied the effects that inorganic zeolite powder have on structurally different copolymer [poly(propylene-co-ethylene)] and terpolymer [poly(propylene-co-ethylene-co-l-butene)] systems and the possibility of preparing suitable porous composite films. The impact strength and yield stress of the composites did not improve upon any further loading of zeolite, but the modulus increased gradually with respect to the filler loading. The experimental modulus of each of the two systems was compared with theoretical models. We performed a morphological study of the filler mixing efficiency and image analysis. The number-, weight-, and z-average air hole diameters were compared with respect to the draw ratio as well as the zeolite loading. The experimental results suggest that these two matrices can provide a new choice for preparing future multiphase polymeric porous films by stretching them unidirectionally. In particular, we suggest that a 40 wt% zeolite loading at a draw ratio of 4 is useful for porous film applications.

• 한국세라믹학회지
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• 제43권8호
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• pp.486-491
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• 2006

A new $TiN-Ti_5Si_3$ bulk composite was synthesized from preceramic, inorganic polymer (methylpolysilsesquioxane) and $TiH_2$ filler powders via polymer pyrolysis. Using this process, ceramics with high melting points can be produced relatively easily to a near net shape. The $TiN-Ti_5Si_3$ composite oxidized slowly during heating to $1000^{\circ}C$. During heating at the temperatures of at 700 and $800^{\circ}C$, TiN oxidized to Rutile-$TiO_2$ whereas $Ti_5Si_3$ resisted to oxidation. The oxide scale formed consisted primarily of $TiO_2$ containing $Ti_5Si_3$.