• ETRI Journal
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• 제34권2호
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• pp.226-234
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• 2012

The novelty of this study resides in the fabrication of stoichiometric and stress-reduced $Si_3N_4/SiO_2/Si_3N_4$ triple-layer membrane sieves. The membrane sieves were designed to be very flat and thin, mechanically stress-reduced, and stable in their electrical and chemical properties. All insulating materials are deposited stoichiometrically by a low-pressure chemical vapor deposition system. The membranes with a thickness of 0.4 ${\mu}m$ have pores with a diameter of about 1 ${\mu}m$. The device is fabricated on a 6" silicon wafer with the semiconductor processes. We utilized the membrane sieves for plasma separations from human whole blood. To enhance the separation ability of blood plasma, an agarose gel matrix was attached to the membrane sieves. We could separate about 1 ${\mu}L$ of blood plasma from 5 ${\mu}L$ of human whole blood. Our device can be used in the cell-based biosensors or analysis systems in analytical chemistry.

• 한국산학기술학회:학술대회논문집
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• 한국산학기술학회 2011년도 춘계학술논문집 1부
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• pp.144-146
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• 2011

Al-MCM-48 molecular sieves (Si/Al = 25, 50, 75 and 100) were synthesized hydrothermally using cetyltrimethyl ammonium bromide as the structure directing template. The orderly arrangement of mesopores was evident from the low angle X-ray diffraction patterns and TEM images. The catalytic performance was evaluated in the vapour phase isopropylation of phenol with isopropyl acetate. Phenol conversion decreased with increase in the Si/Al ratio of the catalysts. The major reaction product was 4-isopropyl phenol (selectivity: 78%). Delocalization of phenolic oxygen electron pair over the aromatic ring promoted para-selective alkylation. Such delocalization could be aided by the hydrophilic surface of the molecular sieves. Though ester was used as the alkylating agent, phenyl isopropyl ether was not formed

• Bulletin of the Korean Chemical Society
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• 제20권6호
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• pp.715-719
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• 1999

The incorporation of cobalt into mesoporous molecular sieves MCM-41 and MCM-48 was carried out. Co-PO/MCM41 and Co-PO/MCM48 were prepared using Co(II) acetate solution adjusted to pH = 3.0 with phosphoric acid by the incipient wetness method. Photoacoustic spectroscopy (PAS) was used to study the local environments of Co(II) incorporated into mesopores. The band around 500 nm in PAS of as-prepared Co-PO/MCM41 and Co-PO/MCM48 with Co(II) acetate solution was changed to triplet bands around 600 nm. This could be assigned to the 4 A2(F)-> 4T1(P) transition of Co(II) surrounded tetrahedrally by oxygen ions after calcination. It may be attributable to that the octahedral cobalt species containing phosphate ligands in coordination sphere reacting with framework's silanol groups to be dispersed atomically onto the surface of mesoporous molecular sieves as a tetrahedral species. This is unlike that the Co in Co-Cl/MCM41 and direct-synthesized Co-MCM41 transforms to Co oxide phase upon calcination. Co-PO/MCM41 and Co-PO/MCM48 were stable while treated with water.

• Bulletin of the Korean Chemical Society
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• 제20권3호
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• pp.291-296
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• 1999

The immobilization of APTMS(3-(2-aminoethylamino)propyltrimethoxysilane) and AAPTMS(3-(2-(2-aminoethyl)aminoethylanino)propyltrimethoxysilane) on the surface of high quality mesoporous molecular sieves MCM-41 and MCM-48 have been confirmed by F.T.-IR spectroscopy, Raman spectroscopy, 29Si solid state NMR, and a surface polarity measurement using Reichardt's dye. The formation of metal (Co(Ⅱ), Ni(Ⅱ), and Cu(Ⅱ)) complexes by immobilized aminosilanes have been investigated by photoacoustic spectroscopy(PAS). The assignment of UV-Vis. PAS bands makes it possible to identify the structure of metal complexes within mesoporous molecular sieves. Co(Ⅱ) ion may be coordinated mainly in a tetrahedral symmetry by two APTMS onto MCM-41, and in an octahedral one by two AAPTMS. Both Ni(Ⅱ) and Cu(Ⅱ) coordinated by aminosilanes within MCM-41 form possibly the octahedral complexes such as [Ni(APTMS)2(H20)2]2+, [Ni(AAPTMS)2]2+, [Cu(APTMS)2(H2O)2]2+, and [Cu(AAPTMS)(H2O)3]2+, respectively. The PAS band shapes of complexes onto MCM-48 are similar to those of corresponding MCM-41 with the variation of PAS intensity. Most of metal ion(Ⅱ) within MCM-41 and MCM-48 are coordinated by aminosilanes without the impregnation on the surface.

• 한국산학기술학회:학술대회논문집
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• 한국산학기술학회 2012년도 춘계학술논문집 1부
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• pp.431-435
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• 2012

Aluminum containing mesoporous molecular sieves Al-SBA-1 ($n_{Si}/n_{Al}$= 2, 5, 10, 15) was synthesized with a one-step method, and the catalyst was characterized with powder X-ray diffraction (XRD), nitrogen adsorption-desorption, thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR). Finally, we studied the catalytic activities of Al-SBA-1 molecular sieves in Pechmann reaction of 3-methoxyphenol and Ethyl acetoacetate to get 7-methoxy-4-methyl coumarin. Four parameters reaction temperature, time, catalyst weight and reactants ratio were optimized.

• Bulletin of the Korean Chemical Society
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• 제31권1호
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• pp.100-103
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• 2010

In this study, NO reduction behaviors of copper-loaded mesoporous molecular sieves (Cu/MCM-41) have been investigated. The Cu loading on MCM-41 surfaces was accomplished by a chemical reduction method with different Cu contents (5, 10, 20, and 40%). $N_2/77$ K adsorption isotherm characteristics, including the specific surface area and pore volume, were studied by BET's equation. NO reduction behaviors were confirmed by a gas chromatography. From the experimental results, the Cu loading amount on MCM-41 led to the increase of NO reduction efficiency in spite of decreasing the specific surface area of catalysts. This result indicates that highly ordered porous structure in the MCM-41 and the presence of active metal particles lead the synergistical NO reduction reactions due to the increase in adsorption energy of MCM-41 surfaces by the Cu particles.

• Bulletin of the Korean Chemical Society
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• 제18권6호
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• pp.663-665
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• 1997

• Bulletin of the Korean Chemical Society
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• 제21권2호
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• pp.251-258
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• 2000

• 한국식품영양과학회지
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• 제38권8호
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• pp.1062-1068
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• 2009

DAG 합성율이 가장 높은 몰비율을 선정하기 위하여 GMO와 CLA의 몰비율을 1:1, 2:1 그리고 3:1로 하고 Lipozyme TLIM은 기질 질량의 20%를 사용하여 반응하였다. 그 결과 총 DAG의 함량은 1 hr일 때 높게 나타나 몰비율이 1:1, 2:1, 3:1(GMO:CLA)일 경우 각각 42.6, 54.4 그리고 54.6 area%로 나타났고, DAG 함량이 높은 2:1과 3:1의 기질몰비율 조건 중 MAG와 TAG의 함량이 낮았던 2:1 비율을 가장 적합한 비율로 선정하였다. 적합한 몰비율로 선정된 GMO와 CLA의 몰비율 2:1에 효소량을 2%, 5%, 10% 그리고 20%를 사용하여 효소량에 따른 DAG 합성율을 살펴 본 결과, 효소량을 10% 사용하였을 경우, 반응 6 hr에서 56.2 area%의 가장 높은 DAG 함량을 나타내었다. 이어 Lipozyme TLIM을 10% 사용하여 GMO와 CLA의 몰비율 2:1에 molecular sieves를 전체 기질 질량의 10% 사용하여 molecular sieves 첨가의 유, 무에 따른 DAG 합성율을 알아보았다. 그 결과 효소량을 5%를 사용하여 반응하였을 경우 molecular sieves를 첨가하지 않았을 때보다 총 DAG 함량이 약 30%의 증가율을 보였고, 효소량을 10% 사용하였을 경우 23%의 증가율을 보였다. 이상에서 DAG가 가장 많이 합성된 반응조건은 몰비율이 GMO와 CLA가 2:1이고, Lipozyme TLIM과 molecular sieves의 양이 각각 기질 질량의 10%씩 사용되었을 때이었다. 이 반응 조건으로 6 hr 반응하였을 때 최대의 DAG량이 생성되어 그 함량은 69 area%로 나타났으며, 1,3-DAG과 1,2-DAG의 지방산 조성변화를 살펴 본 결과 1,2-DAG의 지방산 조성 중 CLA의 함량은 반응 시간이 지날수록 증가한 반면, 1,3-DAG의 CLA 함량은 1 hr에서 24 hr까지 증가하였다가 72 hr에서 감소함을 보였다.

• 공업화학
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• 제29권1호
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• pp.122-126
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• 2018

비이온성 계면활성제 수용액 중에서 $Na_2SiO_3$와 $H_2SiF_6$의 빠른 반응을 통하여 메조포러스 분자체를 제조하였다. 침전은 수초 이내에 형성되었으며, 시료의 XRD분석은 d-spacing이 3.1-5.8 nm인 잘 발달된 피크를 나타내어 메조포러스분자체임을 확인할 수 있었다. 비표면적은 비이온 계면활성제에 따라 $290-1,018m^2/g$의 큰 값을 나타내었으며, 기공분포는 2.5-3.1 nm의 일정한 값을 보여주었다. SEM을 통해 관찰한 입자의 모양은 크기가 ${\sim}0.5{\mu}m$로 균일하고 잘 분리된 구형이었으며, TEM은 기공의 형태가 일정크기의 벌레구멍 모양임을 보여주었다.