• 한국건축시공학회:학술대회논문집
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• 한국건축시공학회 2021년도 가을 학술논문 발표대회
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• pp.133-134
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• 2021

Limestone-calcined clay-Cement (LC3) concrete provides a solution for sustainability, durability, and profitability of concrete industry. This study shows experimental studies of the macro properties (residual compressive strength), the meso properties (mesoscopic images), and micro properties (thermogravimetric (TG) analysis, X-ray powder diffraction (XRD), FTIR spectra, Raman spectra, Mercury intrusion porosimetry, and SEM) of LC3 paste with various mixtures and at high elevated temperatures (20 ℃, 300 ℃, 550 ℃ and 900 ℃). We find (1) Regarding to macro properties, LC3 cementitious materials are at a disadvantage in compressive strength when the temperature is higher than 300 ℃. (2) Regarding to meso properties, when the temperature reached 550 ℃, all samples generated more meso cracks. (3) Regarding to micro properties, first, as the substitution amount increases, its CH content decreases significantly; second, at 900 ℃, for samples with calcined clay, a large amount of gehlenite crystalline phase was found; third, at elevated temperatures (20 ℃, 300 ℃, 550 ℃ and 900 ℃), there is a linear relationship between the residual compressive strength and the cumulative pore volume; fourth, at 900 ℃, a large amount of dicalcium silicate was generated, and damage cracks were more pronounced. The experimental results of this study are valuable of material design of fire resistance of LC3 concrete.

• 폴리머
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• 제38권2호
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• pp.257-264
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• 2014

본 연구에서는 나노크기의 실리카 입자를 2차 아미노기를 가지는 dipodal 형태의 실란커플링제인 bis[3-(trimethoxysilyl)propyl]ethylenediamine(BTPED)으로 표면 개질한 후, 실리카에 도입되는 2차 아미노기인 N-H기와 마이클 부가 반응이 가능한 acrylate기를 가지는 3-(acryloyloxy)-2-hydroxypropyl methacrylate(AHM)로 표면 처리를 하여 중합 반응성 methacrylate기를 도입하는 연구를 수행하였다. 1 분자에 2차 아미노기를 2개 가지는 BTPED와 마이클 부가 반응성이 있는 acrylate기와 부가 반응성이 없는 methacrylate기를 각각 1개씩 가지는 AHM을 사용하여 BTPED와 AHM의 투입량 및 개질 반응 시간의 변화가 실리카 표면의 methacrylate기 도입에 미치는 영향을 Fourier transform infrared spectroscopy(FTIR), elemental analysis(EA)와 액체 및 고체 상태 cross polarization magic angle spinning(CP/MAS) nuclear magnetic resonance spectroscopy(NMR)법을 사용하여 분석하였다. 실리카 표면에 BTPED 를 도입하는 반응은 1시간 내에, BTPED로 개질된 실리카의 N-H기에 대한 AHM의 acrylate기와의 마이클 부가 반응에 따른 methacrylate기 도입은 2시간 내에 반응이 각각 완결됨을 확인하였다. 또한 BTPED로 개질된 실리카에 대하여 투입되는 AHM의 몰 비가 증가할수록 N-H기와 acrylate기의 마이클 부가 반응으로 인한 methacrylate기의 도입이 증가하였으며 이는 AHM을 도입했을 때 나타나는 FTIR 스펙트럼의 C=O 피크 면적 변화로 확인하였다. 위의 결과를 EA 및 고체 상태 $^{13}C$ 및 $^{29}Si$ NMR 분석으로도 확인하였다.

• 폴리머
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• 제37권1호
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• pp.5-14
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• 2013

본 연구에서는 UVB-313(자외선 파장 290-315 nm) 노출 하에 smooth HDPE 지오멤브레인과 flexible PP 지오멤브레인에 대한 자외선 노출의 영향을 평가하였다. 인장특성, 용융지수, 표준 및 고압 산화유도시간 및 FTIR/ATR 결과들을 고찰하였다. 노출된 지오멤브레인 시료의 인장특성은 변하지 않았지만, HDPE 지오멤브레인보다 flexible PP 지오멤브레인의 경우 산화방지제의 감소가 더 큼을 알 수 있었다. 대표적인 현장온도 $20^{\circ}C$에서의 산화방지제의 수명을 예측하기 위하여 외삽에 의한 Arrhenius 모델을 적용하였다. 자외선 노출 전후의 HDPE 지오멤브레인 시료는 용융지수의 큰 차이는 없었지만 flexible PP 지오멤브레인은 가교발생으로 인한 용융지수 감소가 발생하였다. FTIR 스펙트럼으로부터 자외선에 노출된 시료의 경우 카르보닐기와 관련된 $1750\;cm^{-1}$ 부근에서 작은 피크가 발견되었으며, 이는 산화가 진행되었음을 예시하고 flexible PP 지오멤브레인의 경우 $3100{\sim}3500\;cm^{-1}$에서 하이드록시기 또는 하이드로퍼옥사이드기에 의한 새로운 피크를 확인할 수 있었다.

• 대한화학회지
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• 제37권12호
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• pp.995-1002
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• 1993

TMA와 $NH_3$와의 기상 열분해 반응을 in-situ FTIR 분광법으로 관찰하였다. 사용한 spectroscopic reaction cell은 stainless-steel제로 자체 제작한 hexagonal-port chamber로서 2개의 NaCl window를 평행하게 설치하여 1100$^{\circ}C$까지 가열할 수 있으며 또한 이와 같은 높은 온도에서 분광분석이 가능하였다. TMA와 $NH_3$는 혼합 즉시 반응하여 TMA:$NH_3$adduct를 생성하였으며, 500$^{\circ}C$에서그 adduct가 완전분해됨을 FTIR로 확인하였다. TMA와 TMA:$NH_3$adduct의 열분해는 주생성물로$CH_4$을 방출하였다. 기상의 TMA,$NH_3$ 및 TMA:$NH_3$ adduct에 대하여 상온에서 관찰한 IR band들은 문헌값과 대조하여 assign하였다. TMA의 열분해에 대한 kinetic data로부터 이 반응이 1차식으로 일어남을 알 수 있었다.

• 폴리머
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• 제37권4호
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• pp.437-441
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• 2013

A novel sulfonate flame retardant, 1,3,5,7-tetrakis(phenyl-4-sodium sulfonate)adamantane (FR-A), was successfully synthesized from 1-bromoadamantane in sequential four-step reactions involving Fiedel-Crafts phenylation, sulphonation, hydrolysis, and neutralization. The success of synthesis was confirmed by FTIR spectra, $^1H$ NMR spectra, elemental analyses and mass spectra. The effect of FR-A on the flame retardacy of polycarbonate (PC) has been studied. Limiting oxygen index (LOI) and thermogravimetric analysis (TGA) showed that this novel sulfonate flame retardant had effective flame retardancy on polycarbonate (PC). With a small amount (0.08 wt%) of FR-A, the flame retardancy of PC was improved obviously, which got to UL 94 V-0 rating. TGA and DTA curves demonstrated that the additive raised the degradation rate of PC by promoting the quick formation of an insulating carbon layer on the surface, and confirmed that the flame retardant mechanism of PC/FR-A system was similar to potassium diphenylsulfone sulfonate (KSS).

• KIEE International Transactions on Electrophysics and Applications
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• 제4C권4호
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• pp.142-144
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• 2004

To use Poly-dimethylsiloxane (PDMS) for the electrokinetic flow channel, the PDMS surface must be modified to be hydrophilic. With $O_2$ plasma treatment, it is difficult to maintain hydrophilicity for more than one day. In this paper, we present the chemical modification of the PDMS surface using 2-Hydroxyethyl methacrylate (HEMA) to prolong hydrophilicity lifetime. The oxide radicals generated temporarily on the PDMS surface by $O_2$ plasma are grafted with HEMA. Once the PDMS samples have been grafted, they demonstrate improved hydrophilicity retainment and electroosmotic flow characteristics compared to the untreated PDMS and the oxidized PDMS following the $O_2$ plasma process. This phenomenon was verified by the contact angles, Fourier transform infrared (FTIR) spectra and electro osmotic flow rates observed for more than 300 hours.

• Bulletin of the Korean Chemical Society
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• 제27권6호
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• pp.869-874
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• 2006

We have carried out the Glaser oxidative coupling polymerizations of diethynyldiphenylsilane, diethynylmethylphenylsilane,diethynylmethyloctylsilane, and 1,2-diethynyl-1,1,2,2-tetramethyldisilane to afford polycarbosilanes containing diethynyl and organosilane groups in the main chain, such as poly(diethynyldiphenylsilane), poly(diethynylmethylphenylsilane), poly(diethynylmethyloctylsilane), and poly(1,2-diethynyl-1,1,2,2-tetramethyldisilane), respectively. These obtained materials are almost insoluble in common organic solvents such as $CHCl_3$ and THF probably due to the presence of a rigid rod diacetylene group along the polymer main chain. Therefore, the polymers were characterized using several spectroscopic methods in solid state. FTIR spectra of all the polymeric materials show that the characteristic $C \equiv C$ stretching frequencies appear at 2147-2154 $cm ^{-1}$, in particular. The polymers in the solid state exhibit that the strong maximum excitation peaks appear at 260-283 nm and the strong maximum fluorescence emission bands at 367-412 nm, especially. Thermogravimetric analysis of the materials shows that about 55-68% of the initial polymer weights remain at 400 ${^{\circ}C}$ in nitrogen.

• 한국진공학회지
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• 제7권s1호
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• pp.190-196
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• 1998

Amorphous ternary $Si_xC_yN-z$ thin films were obtained by plasma enhanced chemical vapor deposition(PECVD) using $N_2, SiH_4 \;and \;C_2H_4$ as the reaction sources. The chemical state were characterized by x-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy(FTIR). The optical properties of the thin films were investigated by UV-visible spectrophotometer and ellipsometer, and the optical band gaps of thin films were determined from corresponding transmittance spectra following Tauc equation.

• Tribology and Lubricants
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• 제3권2호
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• pp.44-49
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• 1987

Molecular alignment has been postulated as influencing non-Newtonian behavior of liquid lubricants containing various additives. Four blended lubricants, two synthetic and two mineral were analyzed by FTIR spectroscopy. All of the lubricants exhibited polarization changes in their infrared emission spectra at 60$\circ$C under shear. For this work a special mockup journal bearing was constructed to seperate load and shear effects. At a temperature of 100$\circ$C polarization by shear was always reduced, presumably by Browninn motion. This work should be useful in pointing to the shear-sensitive factors. The presence of of a VI improving additive is manifested by the independence of the infrared emissivity with temperature at several wavelengths; a lubricant without a VI improver generally shows a decrease of emissivity at higher temperature.

• 한국전기전자재료학회논문지
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• 제14권2호
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• pp.133-138
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• 2001

We studied the optical properties of poly(3-hexylthiophene) for applying to the emitting material of organic electro luminescent device. The infrared spectrum and NMR of synthesized polymer gave good evidence for the conjugation of 3-hexylthiophene monomer unit. We confirmed that poly(3-hexylthiophene) contains the HT(head-to-tail)-HT(head-to-Tail) linkage larger than 65% based on NMR analysis. FTIR and raman spectroscopy show that poly(3-hexylthiophene) has two main vibration levels which have an energy about 0.18eV and 0.36eV. Electronic absorption spectra shifted to the shorter wavelength with increasing temperature, which is related to a conformational transition of the polymer. Photoluminescence spectrum generated at low temperature(10K) is separated at 669nm, 733nm and 812nm that it's because of phonon energy generated from the lattice vibration.