• 공업화학
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• 제9권7호
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• pp.1047-1052
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• 1998

본 연구에서는 시판용 99.8% 금속알루미늄을 정전류 방식을 이용하여 황산, 수산, 인산 및 크롬산 전해조에서 양극산화를 행하여 다공성 알루미나 막을 제조하였다. 양극산화시 전해액의 종류에 따른 반응온도, 전해액의 농도 및 전류밀도에 따라 형성되는 다공성 알루미나 막의 세공직경과 분포, 막의 두께 및 형태와 결정구조를 조사함으로서 각 전해질 용액하에서의 최적 반응조건을 결정하고 우수한 다공성 알루미나 막을 제조하고자 하였다. 황산, 수산전해질하에서는 한외여과(Ultrafiltration)막이, 인산, 크롬산전해질하에서는 정밀여과(Microfiltration)막의 얻어짐을 알수 있었다. 황산, 수산 및 인산 전해조에서 제조된 막의 결정구조는 무정형임을 알 수 있으며, 크롬산 전해조에서 제조된 막은 ${\gamma}-Al_2O_3$의 결정구조를 보이고 있다.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2011년도 제36회 춘계학술대회논문집
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• pp.85-88
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• 2011

세계적인 환경보호 추세에 발맞추어 단일 추진제 역시 강한 독성을 가지는 Hydrazine 대신 새로운 친환경 추진제를 찾으려는 노력이 계속되고 있다. 그 중 이온성 액체 추진제는 Hydrazine과 비교하여 낮은 독성, 높은 밀도, 그리고 높은 비추력을 가지고 있다. 이들 이온성 액체 추진제는 연소실 온도가 높아 감마 알루미나 등등의 촉매 지지체는 버틸 수가 없다. 따라서 고온에 안정적인 성능을 보이는 촉매가 필요하다. 바륨이 담지된 알루미나는 고온에서 Hexaaluminate로 변환될 수 있으며 그 열적 특성 또한 감마 알루미나보다 우수하다. 바륨이 담지된 알루미나에 백금을 올린 촉매의 특성을 알아보기 위해 $1300^{\circ}C$, $1400^{\circ}C$ 2시간 가열한 후 XRD, SEM, EDS, BET와 Drop test를 진행하였다.

• 공학논문집
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• 제2권1호
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• pp.139-145
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• 1997

촉매연소용 촉매담체인 $\gamma$-$Al_2O_3$의 열안정화에 미치는 Ba의 첨가 효과에 대하여 연구하였다. Ba의 첨가는 $Ba(No_3)_3$.$6H_2O$를 $\gamma$-$Al_2O_3$ 분말에 wet impergnation시키는 방법으로 행하였다. Ba는 $\gamma$-$Al_2O_3$의 소결을 억제함으로써 $\gamma$-$Al_2O_3$의 열안정화에 효과적인 첨가제임을 확인하였으며 최적의 첨가량은 전체 열처리 조건에서 5 mol%임을 알 수 있었다. 이러한 Ba첨가에 의한 열안정화 효과는 이온반경이 큰 $Ba^{2+}$이온이 $\Al^{3+}$이온의 자리에 치환하여 $\Al^{3+}$이온의 표면 확산을 억제하는 효과에서 기인하는 것으로 사료된다.

• 한국세라믹학회지
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• 제54권2호
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• pp.102-107
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• 2017

The dependence of the IR optical properties of PMMA/$Al_2O_3$ nanocomposite on the alumina content was investigated in the wavelength range of $3500-2800cm^{-1}$. The samples were prepared via emulsion polymerization technique using oleic acid as a coupling agent. Grafting density calculations were carried out by means of elemental analysis CHN to yield the best coupling agent content. FTIR analysis confirmed the existence of a chemical bond between aluminum oxide and oleic acid. The outcomes of XRD analyses showed the presence of cubic gamma aluminum oxide in the nanocomposite, in contrast to the amorphous nature of PMMA. TEM images showed the core-shell morphology of the particles other than pristine PMMA. Optical constants of the nanocomposite were calculated based on FTIR spectra and the Kramers-Kronig equations. The presence of nano alumina modified some of the optical indexes in IR region.

• 한국세라믹학회지
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• 제25권6호
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• pp.585-592
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• 1988

Aluminum sec-butoxide was synthesized from aluminum foil and alcohol. The characteristics of the alumina powder prepared from the synthesized alkoxide by the Yoldas method were studied. As a result of measuring the synthesized aluminum sec-butoxide by GC, the purity of the synthesized alkoxide was 98.7% on the basis of commercial alkoxide and the yield was 78.5%. A127-MASNMR analysis shows that powders dried at 9$0^{\circ}C$ and $\alpha$-Al2O3 have 6-cordinated structure and ${\gamma}$-Al2O3 has 4-coordinated structure. The characteristics of alumina powder prepared from the synthisized alkoxide showed the same characteristics with the alumina powder prepared from the commercial alkoxide.

• 대한화학회지
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• 제33권2호
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• pp.263-270
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• 1989

금속알루미늄 조각과 alcohols을 반응시켜 Al-alkoxides를 합성하였으며 이것을 가수분해하여 얻은 Al-hydroxides와 시약 AlCl3로부터 얻은 Al-hydroxides를 여러 온도에서 소성하여 여러 상의 고순도 $Al_2O_3$를 제조하였다. 제조한 ${\gamma}$와 ${\eta}$상 알루미나의 촉매적 특성을 알아보았고, $Al(OH)_3$로부터 ${\alpha}-Al_2O_3$의 생성과정을 속도론적으로 고찰하였다.

• 한국세라믹학회지
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• 제39권10호
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• pp.1007-1010
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• 2002

마이크로파 가열을 이용하여 ${\gamma}-Al_2O_3와\;Na_2SO_4$ 분말 혼합물로부터 알파 알루미나 판상체 입자를 합성하였다. 마이크로파를 이용하여 합성된 알루미나 입자의 크기와 입자분포를 마이크로파 이용 없이 동일한 혼합물로부터 합성된 분말과 비교하였다. 마이크로파를 이용하여 합성된 시료는 마이크로파 사용 없이 합성된 시료에 비하여 입자크기가 작고 입자분포가 좁음을 알 수 있었다.

• 한국응용과학기술학회지
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• 제16권2호
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• pp.163-170
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• 1999

Spherical alumina powders were prepared by the controlled hydrolysis of aluminum iso-propoxide in a solution consisting of n-octyl alcohol and acetonitrile. As aluminum alkoxide's concentration increased, the particle size was increased and size distribution was more broad. As-prepared particle morphology was not spherical when acetonitrile volume fraction was increased over than 60%. As-prepared amorphous powders crystallized to ${\gamma}$-alumina at $1000^{\circ}C$ and converted to ${\alpha}$-alumina at $1150^{\circ}C$. The particle morphology was retain after crystallization ${\alpha}$-alumina. When aluminum iso-propoxide was used as aluminum source, the optimum preparation condition of spherical alumina was 0.1M AIP, 0.2M H2O, $0.1g/{\ell}$ HPC with a volume fraction (1/1) of the n-octyl alcohol/acetonitrile, 10min of reaction time and 30min of aging time.

• 환경위생공학
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• 제11권3호
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• pp.29-35
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• 1996

Numerical solutions were obtained to the model equations for various parameters characterizing the pore structure, effective internal diffusion and the chemical reaction constant. The conversion was decreased with the cause of pore closure at the surface of reacting particles, reduction of porosity, surface area of reaction and effective diffusion coefficient in the solid with the progress of reaction. Total conversion was strongly depend on the local conversion at surface. According to the decreasing of impregnated concentration of the copper oxide and the increase of the flue gases concentration, total conversion was increased. And the conversion were affected by gas flow rate and pore size distribution of the reacting solid.

• Korean Chemical Engineering Research
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• 제61권2호
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• pp.226-233
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• 2023

To create an environmentally sustainable fuel with a low sulfur concentration, requires alternative sulfur removal methods. During the course of this study, a high surface gamma alumina-supported ZnO nanocatalyst with a ZnO/-Al₂O₃ ratio of 12% was developed and tested for its ability to improve the activity of the oxidative desulfurization (ODS) process for the desulfurization of kerosene fuel. Scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) were used to characterize the produced nanocatalyst. In a digital batch baffled reactor (20~80 min), the effectiveness of the synthesized nanocatalyst was tested at different initial concentrations of dibenzothiophene (DBT) of 300~600 ppm, oxidation temperatures (25~70 ℃), and oxidation periods (0.5, 1, and 2 hours). The baffles included in the digital baffled batch reactor resist the swirling of the reaction mixture, thus facilitating mixing. The ODS procedure yielded the maximum DBT conversion (95.5%) at 70 ℃ with an 80-minute reaction time and an initial DBT level of 600 ppm. The most precise values of kinetic variables were subsequently determined using a mathematical modelling procedure for the ODS procedure. The average absolute error of the simulation findings was less than 5%, demonstrating a good degree of agreement with the experimental results acquired from all runs. The optimization of the operating conditions revealed that 99.1% of the DBT can be removed in 140 minutes.