• Korean Chemical Engineering Research
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• 제54권5호
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• pp.712-718
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• 2016

Y 제올라이트로부터 합성한 메조 포러스 물질을 지지체로 사용한 백금 촉매를 n-octadecane의 수첨업그레이딩 반응을 통한 항공유 제조에 적용 하였다. Y 제올라이트를 골격 구성물질로 사용하여 메조 포러스 알루미노실리케이트($MMZ_{HY}$)를 합성 하였다. $Pt/MMZ_{HY}$ 촉매상에서 Mg 첨가가 n-octadecane의 수첨업그레이딩 반응에 미치는 영향을 고찰 하였다. 촉매의 특성은 X 선 회절, 질소 흡착, 승온환원, 암모니아승온탈착 및 흡착 피리딘 적외선 분광법으로 수행 하였다. 본 연구에서 Mg가 2 wt% 첨가된 $Pt/MMZ_{HY}$ 촉매가 가장 높은 항공유 수율을 보였는데, 이는 Mg의 첨가에 의해 Pt금속의 분산도와 환원도가 증가할 뿐만 아니라, 산점의 양과 세기가 증가하기 때문이다. 또한 $PtMg/MMZ_{HY}$ 촉매 상에서 이소 파라핀에 대한 선택도가 80 % 이상임을 확인하였다.

• 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.

• Bulletin of the Korean Chemical Society
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• 제28권11호
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• pp.1985-1992
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• 2007

Ordered mesoporous silica (MCM-41) materials with different textural properties were prepared using alkyl (dodecyl, cetyl, eicosane) trimethyl ammonium bromide (DTAB, CTAB, ETAB, respectively) as structure directing surfactants, functionalized with amine groups and used as adsorbent for the toxic metal ions, Cr (VI), As (V), Pb (II) and Hg (II). Amino functionalization of mesoporous MCM-41 was achieved by cocondensation of N-[3-(trimethoxysilyl)-propyl] aniline with tetraethyl orthosilicate. Adsorption isotherm and adsorption capacity of the amine functionalized materials for Cr (VI), As (V), Pb (II) and Hg (II) ions were followed by inductively coupled plasma mass spectrometry (ICP-MS). Results demonstrate that amine functionalized MCM-41 prepared with ETAB showed higher adsorption capacity for Cr (VI), As (V), Pb (II) and Hg (II) ions in comparison to MCM-41 prepared with CTAB and DTAB. The higher adsorption capacity for MCM-41(ETAB) was correlated with amine content in the material (determined by CHN analysis) and relative decrease in pore volume and pore diameter. X-ray diffraction (XRD) analysis, nitrogen adsorptiondesorption measurements and Fourier Transform infrared spectrometry (FTIR) were used to follow the changes in the textural parameters and surface properties of the mesoporous materials as a result of amine functionalization to correlate with the adsorption characteristics. The adsorption process was found to depend on the pH of the medium.

• 한국자기공명학회논문지
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• 제1권2호
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• pp.126-140
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• 1997

Mesoporous MCM-41 gallosilicate material was synthesized through shifting through shifting gallosilicate polymer equilibrium towards a MCM-41 phase by addition of acid. The location of Cu(II) exchanged into MCM-41 and its interaction with various adsorbate molecules were investigated by electron spin responance and electron spin echo modulation spectroscopies. It was found that in the fresh hydrated material, Cu(II) is octahedrally coordinated to six water molecules. This species is located in a cylindrical channel and rotates rapidly at room temperature. Evacuation at room temperature removes three of these water molecules, leaving the Cu (II) coordinated to three water molecules and anchored to oxygens in the channel wall. Dehydration at 45$0^{\circ}C$ produces one Cu (II) species located in the inner surface of a channel as evidenced by broadening of its ESR lines by oxygen. Adsorption of polar molecules such as water, methanol and ammonia on dehydrated CuNa-MCM-41 gallosilicate material causes changes in the ESR spectrum of Cu (II), indicating the complex formation with these adsorbates. Cu (II) forms a complex with six molecules of methanol as evidenced by an isotropic room temperature ESR signal and ESEM data like upon water adsorption. Cu(II) also forms a complex containing four molecules of ammonia based on resolved nitrogen superhyperfine interaction.

• Journal of Electrochemical Science and Technology
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• 제5권2호
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• pp.58-64
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• 2014

The surface of an ordered mesoporous silica (OMS) was functionalized using 1H,1H,2H,2H-perfluorooctyltrimethoxysilane at $20^{\circ}C$ and $60^{\circ}C$. It was shown that only elevated temperature allows lyophobic properties on the walls of OMS, eventually preventing pore flooding with nonaqueous electrolytes. The functionalized OMSs (OMS-F) were characterized with various techniques: wettability test, $N_2$ sorption measurement, high-resolution transmission electron microscopy (HR-TEM). Cathodes of $10mg/cm^2$ loading were prepared with a commercial Pt/C catalyst and polyvinylidene fluoride (PVDF, 2.5 wt.%) binder using a typical doctor blade method on a commercial gas diffusion layer (GDL) in the presence or in the absence of OMS-F additives. Subsequent discharge-charge curves were taken in a 1M LiTFSI-TEGDME electrolyte at 60oC in pure oxygen atmosphere. It was found that the discharge capacity was significantly affected by OMS-F: 5 wt.% of additive extended discharge capacity by a factor 1.5. On the other hand, a similar OMS material but synthesized at $20^{\circ}C$ did not show lyophobic properties and deteriorated cathode capacity.

• Transactions on Electrical and Electronic Materials
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• 제12권3호
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• pp.119-122
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• 2011

A series of mesoporous silicalites was synthesized using different compositions of tetraethylorthosilicate and methyltriethoxysilane (MTES) as the silica source. Cetyltrimethylammonium bromide was used as the organic template. Their detailed pore structures were investigated by transmission electron microscopy, X-ray diffraction, and N2 adsorption method. The thermal properties of these silicalites were studied by thermogravimetric analysis. The increased amount of MTES destroyed mesoporous channels and reduced pore sizes from 3.4 nm to 2.8 nm in calcined silicalites. The calcined silicalite transformed completely into an amorphous state at 30% MTES loading. Methyl pending groups of MTES hindered the structural ordering of ≡Si-O- frameworks, resulting in an amorphous structure. This was caused by the insufficient formation of supramolecular assembly with the organic template. No capillary condensation step was found in MS 7/3 silicalite. The other capillary condensation steps shifted toward the lower relative pressure with increasing MTES content, indicating the reduction of pore sizes.

• 한국재료학회지
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• 제28권1호
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• pp.24-31
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• 2018

This study reports an environment-friendly synthetic strategy to process nickel oxide nanocrystals. A mesoporous nickel oxide nanostructure was synthesized using an environmentally benign biomimetic method. We used a natural rambutan peel waste resource as a raw material to ligate nickel ions to form nickel-ellagate complexes. The direct decomposition of the obtained complexes at $700^{\circ}C$, $900^{\circ}C$ and $1100^{\circ}C$ in a static air atmosphere resulted in mesoporous nickel oxide nanostructures. The formation of columnar mesoporous NiO with a concentric stacked doughnuts architecture was purely dependent on the suitable direct decomposition temperature at $1100^{\circ}C$ when the synthesis was carried out. The prepared NiO nanocrystals were coated on cotton fabric and their antibacterial activity was also analyzed. The NiO nanoparticle-treated cotton fabric exhibited good antibacterial and wash durability performance.

• Bulletin of the Korean Chemical Society
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• 제29권3호
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• pp.609-614
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• 2008

A periodic mesoporous organosilica material was synthesized by microwave heating (PMO-M) using 1,2-bis(trimethoxysilyl)ethane as a precursor in a cationic surfactant solution, and textural properties were compared with those of the product produced by conventional convection heating (PMO-C). These synthesized materials were characterized using XRD, TEM/SEM, N2 adsorption isotherm, 29Si and 13C NMR, and TGA, which confirmed their good structural orders and clear arrangements of uniform 3D-channels. Synthesis time was reduced from 21 h in PMO-C to 2-4 h in PMO-M. PMO-M was made of spherical particles of 1.5-2.2 m m size, whereas PMO-C was made of decaoctahedron-shaped particles of ca. 8.0 m m size. Effect of synthesis temperature, time, and heating mode on the PMO particle morphology was examined. The particle size of PMO-M could be controlled by changing the heating rate by adjusting microwave power level. PMO-M demonstrated improved separation of selected organic compounds compared to PMO-C in a reversed phase HPLC experiment. Ti-grafted PMO-M also resulted in higher conversion in liquid phase cyclohexene epoxidation than by Ti-PMO-C.

• 한국세라믹학회지
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• 제45권1호
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• pp.48-53
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• 2008

In order to reduce signal delay in ULSI, an intermetal material of low dielectric constant is required. Ordered mesoporous silica film is proper to intermetal dielectric due to its low dielectric constant and superior mechanical properties. The ordered mesoporous silica film prepared by TEOS (tetraethoxysilane) / MTES (methyltriethoxysilane) mixed silica precursor and Brij-76 surfactant was surface-modified by HMDS (hexamethyldisilazane) treatment to reduce its dielectric constant. HMDS can substitute $-Si(CH_3)_3$ groups for -OH groups on the surface of silica wall. In order to modify interior silica wall, HMDS was treated by two different processes except the conventional spin coating. One process is that film is dipped and stirred in HMDS/n-hexane solution, and the other process is that film is exposed to evaporated HMDS. Through the investigation with different HMDS treatment, it was concluded that surface modification in evaporated HMDS was more effective to modify interior silica wall of nano-sized pores.

• Korean Chemical Engineering Research
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• 제44권4호
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• pp.369-374
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• 2006

$V_2O_5$와 AlMCM-48을 고체상에서 반응시킨 후 소성하면 메조포러스 물질 내에서 V(V) 화학종이 아주 약하게 나타난다. 그러나 환원 과정을 거치면 EPR로 조사할 수 있는 바나딜 $VO^{2+}$ 화학종이 생성된다. $VO^{2+}-AlMCM-48$에 들어있는 바나듐의 화학적 환경을 XRD, EDX, UV-Vis, EPR, $^{29}Si$ and $^{27}Al$ and $^{51}V$ NMR로 조사하였다. 탈수하거나 CO 로 환원하면 바나듐은 MCM-48에 유사 사면체형 $VO^{2+}$ 바나딜 이온 상태로 존재하며 물이 배위되면 찌그러진 팔면체구조로 바뀐다.