• 공업화학
• /
• 제30권3호
• /
• pp.371-378
• /
• 2019

그래핀나노플레이트렛(GnP)이 목재기반 복합보드의 열적 및 난연 특성에 미치는 영향을 조사하기 위하여, 5, 10, 및 20 wt% 등 여러 가지 GnP 함량으로 GnP/재활용 페놀폼(re-PF)/목재 복합보드를 제조하였다. 제조된 복합보드의 열적특성 및 난연성은 열중량분석(TGA) 및 한계산소지수(LOI) 시험을 통하여 각각 분석되었다. 복합보드의 열안정성은 GnP 첨가량에 따라 비례하게 증가하였고, 이 복합보드의 탄화수율(char yield)은 순수 목재보드 대비 최대 22%까지 증가하였다. 복합보드의 LOI 값은 순수 목재보드보다 약 4.8~7.8% 높았다. 또한, 재활용 페놀폼 및 GnP 첨가로 인하여 복합보드의 난연성이 크게 향상되었음을 확인하였다. 이는 열안정성이 높은 재활용 페놀폼과 GnP가 복합보드의 열분해 개시 온도를 지연시키고, 탄화층(char layer)을 보다 조밀하고 두껍게 형성하였기 때문에, 복합보드의 연소 지연효과를 이끌었다. 특히 탄소기반 재료로서 GnP는 탄화층의 형성을 용이하게 하고, 탄화수율을 현저히 증가시켜 재활용 페놀폼에 비하여 난연성에 높은 효과를 나타내었다.

• 폴리머
• /
• 제36권6호
• /
• pp.822-830
• /
• 2012

본 연구에서는 실리카 나노입자를 우수한 내가수분해성을 가지는 dipodal 형태의 bis[3-(trimethoxysilyl)propyl]amine(BTMA) 실란 커플링제로 표면 개질한 후, 실리카에 도입된 BTMA의 2차 아미노기인 N-H기와 마이클 부가반응이 가능한 acrylate기를 1분자당 2개씩 가지는 poly(ethylene glycol)diacrylate(PEGDA)로 표면 처리하여 acrylate기를 실리카 입자 표면에 도입하는 연구를 수행하였다. PEGDA의 몰수 및 3가지 서로 다른 분자량의 PEGDA(M.W. 258, 575, 700) 처리가 실리카 표면에 도입되는 acrylate기의 구조에 미치는 영향을 fourier transform infrared spectroscopy(FTIR), elemental analysis(EA, 원소분석) 및 고체 상태 $^{13}C$ cross-polarization magic angle spinning(CP/MAS) nuclear magnetic resonance spectroscopy(NMR)법을 사용하여 분석하였다. 액체상태의 순수 PEGDA와 순수 BTMA를 같은 몰 비로 반응시키면 PEGDA 1분자당 2개씩 존재하는 acrylate기 중 1개 acrylate기는 순수 BTMA의 N-H기와 1:1의 비율로 마이클 부가반응이 일어나 ${\beta}$-amino acid ester를 형성하고, 나머지 1개의 acrylate기는 남아서 중합반응이 가능한 단량체 합성이 가능하다. 하지만, BTMA로 개질된 실리카 입자를 PEGDA와 반응시키면, PEGDA 1분자당 2개씩 결합있는 acrylate기 대부분이 실리카 입자에 결합되어 있는 BTMA의 N-H기와 마이클 부가반응으로 ${\beta}$-amino acid ester를 형성하여, acrylate기의 C=C기 대부분이 C-C로 변화함을 확인하였다.

• Corrosion Science and Technology
• /
• 제7권1호
• /
• pp.50-60
• /
• 2008

The majority of the described experimental results deal with relatively pure aluminium. Variations were made in the pretreatment of the aluminum substrates and an investigation was performed on the resulting changes in oxide layer composition and chemistry. Subsequently, the bonding behavior of the surfaces was investigated by using model adhesion molecules. These molecules were chosen to represent the bonding functionality of an organic polymer. They were applied onto the pretreated surfaces as a monolayer and the bonding behavior was studied using infrared reflection absorption spectroscopy. A direct and clear relation was found between the hydroxyl fraction on the oxide surfaces and the amount of molecules that subsequently bonded to the surface. Moreover, it was found that most bonds between the oxide surface and organic functional groups are not stable in the presence of water. The best performance was obtained using molecules, which are capable of chemisorption with the oxide surface. Finally, it was found that freshly prepared relatively pure aluminum substrates, which are left in air, rapidly lose their bonding capacity towards organic functional groups. This can be attributed to the adsorption of contamination and water to the oxide surface. In addition the adhesion of a typical epoxy-coated aluminum system was investigated during exposure to water at different temperatures. The coating was found to quite rapidly lose its adhesion upon exposure to water. This rapid loss of adhesion corresponds well with the data where it was demonstrated that the studied epoxy coating only bonds through physisorptive hydrogen bonding, these bonds not being stable in the presence of water. After the initial loss the adhesion of the coating was however found to recover again and even exceeded the adhesion prior to exposure. The improvement could be ascribed to the growth of a thin oxyhydroxide layer on the aluminum substrate, which forms a new, water-stable and stronger bond with the epoxy coating. Two routes for improvement of adhesion are finally decribed including an interphasial polymeric thin layer and a treatment in boiling water of the substrate before coating takes place. The adhesion properties were finely also studied as a function of the Mg content of the alloys. It was shown that an enrichment of Mg in the oxide could take place when Mg containing alloys are heat-treated. It is expected that for these alloys the (hydr)oxide fraction also depends on the pre-treatment and on the distribution of magnesium as compared to the aluminium hydroxides, with a direct impact on adhesive properties.

• 한국진공학회:학술대회논문집
• /
• 한국진공학회 1999년도 제17회 학술발표회 논문개요집
• /
• pp.168-168
• /
• 1999

Recently, Fe/Si multilayered films (MLF) have been a focus of interest due to the strong antiferromagnetic (AF) coupling observed in such kind of MLF originates from the same nature as in the metal/metal MLF. In particular, a question of whether the spacer layer in the Fe/Si MLF is metallic or semiconducting is of interest. In spite of various experimental techniques envolved in the study, the chemical composition and the properties of the interfacial regions in the MLF exhibiting the AF coupling is still questionable. The nature of the AF coupling and the interfacial properties of Fe/Si MLF are investigated in this study. A series of Fe/Si MLF with a fixed nominal thickness of Fe(3nm) and a variable thickness of Sk(1.0-2.2nm) were deposited by RF-sputtering onto glass substrates at room temperature. The atomic structures and the actual sublayer thicknesses of the Fe/Si MLF are investigated by using x-ray diffraction. The magnetic-field dependence of the equatorial Kerr effect clearly shows an appearance of the AF coupling between Fe sublayers at tsi = 1.5 - 1.8 nm. the drastic discrepancies between the experimental magnetooptical (MO) and optical properties, and based on the assumption of sharp interfaces between Fe and Si sublayers leads to a conclusion that pure si is absent in the AF-coupled Fe/Si MLF. Introducing in the model nonmagnetic semiconducting FeSi alloy layers between Fe and Si sublayers or as spacer between pure Fe sublayers only slightly improves the agreement between model and experiment. A reasonable agreement between experimental and simulated MO spectra was reached with using the fitted optical properties for the spacer with a typical metallic type of behavior. The results of the magnetic properties measured by vibrating sample magnetometer and magnetic circular dichroism are also analyzed in connection with the MO and optical properties.

• 대한전자공학회논문지
• /
• 제26권6호
• /
• pp.30-37
• /
• 1989

Silane($SiH_4$), methane($CH_4$), diborane(B_2H_6)그리고 phosphine($PH_3$)을 이용하여 rf글로방전분해법으로 PIN형 a-SiC:H/a-Si:H 이종접합 태양전지를 제작하였다. $SnO_2/ITO$층 형성치 태양전지의 효율은 ITO 투명전극만의 경우보다 1.5% 향상되었다. 제작조건은 P층의 경우 $CH_4/SiH_4$의 비를 5로 하고 두께는 $100{\AA}$이었다. I층은 P층위에 증착하였으나 진성이 아니고 N형에 가깝다. 이 I층을 진성으로 바꾸기 위해서 0.3ppm의 $B_2H_6$를 $SiH_4$에 혼합하여 5000${\AA}$증착했다. 또한 N층은 $PH_4/SiH_4$의 비를 $10^{-2}$로 하여 $400{\AA}$ 증착시켰다. 그 결과 입사강도가 15mW/$cm^2$일 때 개방전압 $V_{oc}=O'$단락전류밀도 $J_{sc=14.6mA/cm^2}$, 충진율 FF=58.2%, 그리고 효율 ${eta}=8.0%$를 나타내었다. 빛의 반사에 의한 손실을 감소시키기 위하여 $MgF_2$를 유리기판위에 도포하였다. 이에 의한 효율은 0.5% 향상되어 전체적인 효율은 8.5%였다.

• 통합자연과학논문집
• /
• 제3권3호
• /
• pp.153-156
• /
• 2010

Oxidation behaviors of porous silicon were investigated by the measurement of area of $SiO_2$ vibrational peaks in FT-IR spectra during thermal oxidation of porous silicon at corresponding temperatures. Visible photoluminescent porous silicon samples were obtained from an electrochemical etch of n-type silicon of resistivity between 1-10 ${\Omega}/cm$. The etching solution was prepared by adding an equal volume of pure ethanol to an aqueous solution of HF. The porous silicon was illuminated with a 300 W tungsten lamp for the duration of etch. Etching was carried out as a two-electrode galvanostatic procedure at applied current density of 200 $mA/cm^2$ for 5 min. The porosity of samples prepared was about 80%. After formation of porous silicon, the samples were thermally oxidized at $100^{\circ}C$, $200^{\circ}C$, $300^{\circ}C$, and $400^{\circ}C$, respectively. The growth rate of $SiO_2$ layer of porous silicon was investigated by using FT-IR spectroscopy. The effect of oxidation of porous silicon was presented.

• 한국전기전자재료학회논문지
• /
• 제14권5호
• /
• pp.435-443
• /
• 2001

As power durable RF SAW filters, AL-(0∼2wt%)Cu alloy multi-layered thin electrodes were deposited on 42° LiTaO$_3$ piezoelectric substrates by magnetron sputtering process, and then ladder-type RF SAW filters, satisfying the electrical specification of CDMA transmission band, were fabricated through optimizing SAW resonator structures. The temperature of film electrodes in SAW filter was increased with RF power, and reached the maxima to cause a failure of SAW filters at the cut-off frequencies of the RF filter band. As RF power increases, the electrodes of Al-Cu alloy showed higher power durability than that of pure Al. The multi-layer laminated film of Al-1wt.% Cu/Cu/Al-1wt%Cu resulted in the best power durability up to 4W of RF power. Every film electrode, however, was destroyed within seconds whenever applying a critical RF power to SAW filters, regardless of the composition and structure of film electrodes. The breakdown of film electrodes under FR power seems to believe due to the fatigue of electrodes caused by repetitive cyclic stress of surface acoustic wave, which is amplified as RF power increases.

• 폴리머
• /
• 제34권4호
• /
• pp.294-299
• /
• 2010

아미노실란 처리된 점토를 제조하여, 이를 분자량이 서로 다른 폴리프로필렌(140 kg/mol과 410 kg/mol) 과 상용화제인 무수말레인산 그래프트 폴리프로필렌(50 kg/mol)과 함께 $170^{\circ}C$ 및 $190^{\circ}C$에서 용융혼합법으로 각각의 폴리프로필렌/점토 나노복합체를 제조하였다. 무수말레인산 그래프트 폴리프로필렌과 용융혼합과정에서 낮은 분자량의 폴리프로필렌은 점토 층 사이로 쉽게 침투하여 층간 거리를 58 $\AA$ 이상으로 증가시키지만, 첨가된 점토는 60~80 nm 두께의 응집체로 나노복합체 내에 분산상을 이룬다. 이와 달리 높은 분자량의 폴리프로필렌 기반 나노복합체에서는 점토는 27 $\AA$로 낮은 박리 정도를 보이며, 전반적으로 고른 점토 분산상을 형성한다. 분자 량 및 용융혼합공정의 차이에 따른 폴리프로필렌/점토 나노복합체의 미세 모폴로지 차이로 기계적 물성 및 결정 화거동이 관찰되었으며, 분자량 410(kg/mol)인 폴리프로필렌은 개질된 점토를 1~3 wt% 첨가함으로써 순수 폴 리프로필렌의 연성특성을 유지하면서 향상된 인장강도와 탄성률을 보였다.

• 한국자기학회지
• /
• 제5권1호
• /
• pp.42-47
• /
• 1995

자기 유도 헤드용 FeN 박막을 RF diode reactive 스퍼터 방법으로 Corning 7059 유리 기판 위에 증착하여 그 자기적 특성을 측정하였다. FeN 박막의 자기적 특성은 박막 두께, 가스 압력, 스퍼터 파워, $N_{2}$와 Ar의 유량비에 큰 영향을 받았다. 스퍼터 파워 800 W, 가스 압력 3 mT, 질소와 아르곤의 유량비 6.6 : 100, 단층 박막의 두께를 $1,000\;{\AA}$에서 $6,000\;{\AA}$으로 변화시키며 보자력의 변화를 측정 하였다. 두께가 $30\;{\AA}$인 $SiO_{2}$ 층을 사이층으로 하여 전체 박막 두께를 $6,000\;{\AA}$으로 고정하고 7층까지 증착한 시편의 보자력과 포화 자화값을 측정하였다. 단층 박막 두께에 따른 자화용이 방향의 보자력은 두께가 증가할수록 감소하였으며 $3,000\;{\AA}$ 이상에서는 거의 변화가 없었다. FeN 다층 박막의 경우 층수가 증가함에 따라 보자력은 감소하였다. X 선 회절 선폭으로 부터 결정립의 크기를 계산한 결과 층수가 증가할수록 결정립의 크기가 $200\;{\AA}$에서 $120\;{\AA}$으로 점차 감소하였다. 최소 보자 력은 4층 박막에서 자화 곤란 방향으로 0.4 Oe을 얻었다. 투자율 측정 결과 최대 상대 투자율은 2,900이었으며, 이들 박막의 차단 주파수는 100 MHz 이상이었다.

• 한국전기전자재료학회:학술대회논문집
• /
• 한국전기전자재료학회 2009년도 추계학술대회 논문집
• /
• pp.127-127
• /
• 2009

The most important part of the fabrication solar cells is the anti-reflection coating when excludes the kinds of silicon substrates (crystalline, polycrystalline, or amorphous), patterns and materials of electrodes. Anti-reflection coatings reduce the reflection of sunlight and at last increase the intensity of radiation to inside of solar cells. So, we can obtain increase of solar cell efficiency about 10% using anti-reflection coating. There are many kinds of anti-reflection film for solar cell, such as SiN, $SiO_2$, a-Si, and so on. And, they have two functions, anti-reflection and passivation. However such materials could not perfectly prevent reflection. So, in this work, we investigated the anti-reflection coating with the columnar structure ZnO thin film. We synthesized columnar structure ZnO film on glass substrates. The ZnO films were synthesized using a RF magnetron sputtering system with a pure (99.95%) ZnO target at room temperature. The anti-reflection coating layer was sputtered by argon and oxygen gases. The angle of target and substrate measures 0, 20, 40, 60 degrees, the working pressure 10 mtorr and the 250 W of RF power during 40 minutes. The confirm the growth mechanism of ZnO on columnar structure, the anti-reflection coating layer was observed by field emission scanning electron microscopy (FE-SEM). The optical trends were observed by UV-vis and Elleso meter.