• 공업화학
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• 제27권2호
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• pp.190-194
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• 2016

Tricyclopentadiene (TCPD)는 차세대 고밀도에너지 연료인 tetrahydrotricyclopentadiene의 전구체로서 중요한 화합물이다. 본 연구에서는 이온성 액체가 담지된 메조포로스 실리카 촉매를 이용하여 dicyclopentadiene 소중합 반응을 통한 TCPD 합성에 관한 연구를 수행하였다. 나노기공의 크기가 다른 대표적인 메조포로스 실리카인 MCM-41과 SBA-15에 이온성 액체(IL)를 함침법을 이용하여 담지하고 소중합 촉매를 제조하였다. 음이온 전구체로 copper(I) chloride (CuCl) 또는 iron(III) chloride ($FeCl_3$), 양이온 전구체로 triethylamine hydrochloride (TEAC) 또는 1-butyl-3-methylimidazolium chloride(BMIC)를 사용하여 4가지 종류의 IL을 메조포로스 실리카에 담지하였다. 이온성 액체가 담지된 메조기공의 실리카를 사용하였을 때 이온성 액체만 사용하였을 때보다 TCPD 수율과 dicyclopentadiene (DCPD)의 전환율 측면에서 우수하였다. 특히, MCM-41에 루이스 산도가 낮은 CuCl계 이온성 액체를 담지할 때 TCPD 수율이 가장 높았다.

• 새물리
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• 제68권11호
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• pp.1173-1182
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• 2018

메조포러스 실리카는 강한 친수성과 구조적인 특성으로 인하여 저습환경에서도 이온교환막에 적절한 수화가 일어나도록 할 것이다. 그러므로 메조포러스 실리카와 나피온을 합성한 이온교환막은 낮은 상대습도에서도 우수한 양성자 전도도를 보일 것이다. 메조포러스 실리카와 나피온 합성이온교환막의 이온채널형성 그리고 네트워크를 통한 양성자 이동에 대한 이해는 합성이온교환막을 개발하고 최적화하기 위해 필수적이라 할 수 있다. 이 연구에서는 메조포러스 구조 (mesoporous cellular foam) $SiO_2/Nafion$ 합성이온교환막을 제작하고 양성자 전도도 및 성능을 평가하였다. 또한, 정전기력 현미경(electrostatic force microscopy, EFM)을 사용하여 메조포러스 구조 $SiO_2/Nafion$ 합성 이온교환막의 표면 전하 밀도 측정을 통한 이온 채널의 분포 및 밀도를 분석하였다. 연구는 몇 가지 주목할 만한 결과를 보여주었다. 첫째, 합성이온교환막은 저습환경에서 우수한 양성자 전도도 및 성능을 나타내었다. 둘째, 합성이온교환막은 국부적으로 이온채널의 밀도가 주목할 만하게 높은 지역이 형성되며 동시에 양성자 전도도가 극단적으로 낮은 지역 또한 동시에 형성됨을 확인하였다.

• 분석과학
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• 제24권2호
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• pp.94-104
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• 2011

본 연구에서는 양쪽성 메조 다공성 실리카를 다양한 조건(용매, 계면활성제와 올리고머의 량, 용액의 pH)에서 합성하였다. 메조 다공성 실리카를 사용하여 염소 소독으로 인해 음용수 중에 미량 존재하는 변이원성 물질인 MX (3-chloro-4-(dichloromethyl)-5-hydroxy-2-(5H)-furanone)의 흡착에 관한 특성을 연구하였다. 소수성과 친수성의 양쪽성 폴리우레탄 올리고머를 사용하여 합성된 메조다공성 실리카의 경우 뛰어난 흡착특성을 나타내었다. 그리고 보조 계면 활성제의 경우에는 비이온성이며 분자량이 큰 폴리 에틸렌 프로필렌 옥사이드(PEO-PPO)를 사용하여 합성된 메조 다공성 실리키가 가장 좋은 흡착 특성을 보였다.

• 한국산학기술학회:학술대회논문집
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• 한국산학기술학회 2010년도 추계학술발표논문집 1부
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• pp.313-317
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• 2010

Li, Zr doped mesoporous silica was synthesized in one pot and investigated for low temperature $CO_2$ adsorption. Herein CTAB and TEOS are used as structural directing agent and silica source respectively. The characteristics of the material was obtained from FT IR, XRD, SEM, TG and BET results. ICP AES results revealed the presence of lithium and zirconium. The material possesses high surface area ($962.22m^2g^{-1}$) with mono dispersed particles of about 2 nm. The maximum $CO_2$ adsorption capacity is 5 wt % (50 mg/g) of $CO_2$/g of sorbent at $25^{\circ}C$, which is regenerable at $200^{\circ}C$. This regeneration temperature of the adsorbent is lower than the reported lithium zirconium silicate powder. Until now, there is no report for the synthesis of Li, Zr doped mesoporous silica. The performance studies illustrate that Li, Zr doped mesoporous silica is tunable, regenerable, recyclable and selective sorbent and hence found to be a promising candidate for $CO_2$ adsorption.

• Bulletin of the Korean Chemical Society
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• 제26권11호
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• pp.1653-1668
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• 2005

Assembly of hybrid mesophases through the combination of amphiphilic block copolymers, acting as structuredirecting agents, and silicon sources using low acid catalyst concentration regimes is a versatile strategy to produce large quantities of high-quality ordered large-pore mesoporous silicas in a very reproducible manner. Controlling structural and textural properties is proven to be straightforward at low HCl concentrations with the adjustment of synthesis gel composition and the option of adding co-structure-directing molecules. In this account, we illustrate how various types of large-pore mesoporous silica can easily be prepared in high phase purity with tailored pore dimensions and tailored level of framework interconnectivity. Silica mesophases with two-dimensional hexagonal (p6mm) and three-dimensional cubi (Fm$\overline{3}$m, Im$\overline{3}$m and Ia$\overline{3}$d) symmetries are generated in aqueous solution by employing HCl concentrations in the range of 0.1−0.5 M and polyalkylene oxide-based triblock copolymers such as Pluronic P123 $(EO_{20}-PO_{70}-EO_{20})$ and Pluronic F127 $(EO_{106}-PO_{70}-EO_{106})$. Characterizations by powder X-ray diffraction, nitrogen physisorption, and transmission electron microscopy show that the mesoporous materials all possess high specific surface areas, high pore volumes and readily tunable pore diameters in narrow distribution of sizes ranging from 4 to 12 nm. Furthermore, we discuss our recent advances achieved in order to extend widely the phase domains in which single mesostructures are formed. Emphasis is put on the first synthetic product phase diagrams obtained in $SiO_2$-triblock copolymer-BuOH-$H_2O$ systems, with tuning amounts of butanol and silica source correspondingly. It is expected that the extended phase domains will allow designed synthesis of mesoporous silicas with targeted characteristics, offering vast prospects for future applications.

• 상하수도학회지
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• 제21권1호
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• pp.139-147
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• 2007

For environmental remediation of a contaminated groundwater plume, the use of zero-valent metal represents one of the latest innovative technologies. In this study, the effects of denitrification by zero-valent iron adsorbed in mesoporous silicas have been studied for groundwater contaminant degradation. The mesoporous silica was functionalized with 3-mercaptopropyltrimethoxysilane (MPTS) ligands and the zero-valent iron precipitated in the mesopore of granular silica was made by $FeCl_2$ and $NaBH_4$. Hydrogen was exchanged with $Fe^{2+}$ ions in the granular silicas. And then the ions were reduced by sodium borohydride in the mesoporous silicas. The surface area of the silica determined via the BET method ranged from 858 to $1275m^2/g$. The reductive reaction of nitrate-nitrogen indicated that the degradation of nitrate-nitrogen appeared to be pseudo first-order with the observed reaction rate constant kobs ($0.1619h^{-1}$) and to be directly proportional to the specific surface area. Therefore, the mesoporous silica with nano zero-valent iron proposed as a novel treatment strategy for contaminated groundwater was successfully implemented herein for the removal of nitrate-nitrogen.

• 한국결정학회:학술대회논문집
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• 한국결정학회 2002년도 정기총회 및 추계학술연구발표회
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• pp.49-49
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• 2002

A strategy for the synthesis of more stable and large periodic mesoporous organo-silica materials has been developed for the 2D hexagonal mesoporous organosilica by the core-shell approach using nonionic PEO-PLGA-PEO triblock copolymer templates. The BET surface area of the solvent-extracted hexagonal mesoporous organosilica is estimated to be 1,016 ㎡/g and the pore volume, pore diameter, and wall thickness are 1.447 ㎤/g, 65 Å, and 43 Å, respectively. More hydrophobic PLGA block than the PPO block used for templates of mesoporous silica proves to be quite effective in confining the organosilicates within the PEO phase. Reaction temperature and acid concentration of an initial solution as well as the chemical nature of the bloc k copolymer templates also demonstrate to be important experimental parameters for ordered organosilica mesophase. Moreover, the mesoporous organosilicas prepared with the PEO-PLGA-PEO block templates maintain their structural integrity for up to 25 days in boiling water at 100℃. The mesoporous materials with large pores and high hydrothermal stability prepared in this study has a potential for many applications.

• 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.

• Bulletin of the Korean Chemical Society
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• 제35권12호
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• pp.3465-3474
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• 2014

Porous silica particles are the most prevailing raw material for stationary phases of liquid chromatography. During a long period of time, various methodologies for production of porous silica particles have been proposed, such as crashing and sieving of xerogel, traditional dry or wet process preparation of conventional spherical particles, preparation of hierarchical mesoporous particles by template-mediated pore formation, repeated formation of a thin layer of porous silica upon nonporous silica core (core-shell particles), and formation of specific silica monolith followed by grinding and calcination. Recent developments and applications of useful porous silica particles will be covered in this review. Discussion on sub-$3{\mu}m$ silica particles including nonporous silica particles, carbon or metal oxide clad silica particles, and molecularly imprinted silica particles, will also be included. Next, the individual preparation methods and their feasibilities will be collectively and critically compared and evaluated, being followed by conclusive remarks and future perspectives.

• Elastomers and Composites
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• 제55권4호
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• pp.277-280
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• 2020

In this study, mesoporous hollow silica spheres were synthesized using a polystyrene core and cetyltriammonium chloride (CTACl) as a pore template, and a low-cost water glass instead of expensive tetraethyl orthosilicate (TEOS) as a precursor. In addition, the material was synthesized by varying the concentration of polystyrene. Later, the polystyrene core and CTACl were removed by firing in a high-temperature heat-treatment process. The synthesized product was analyzed by various methods, such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffractometry (XRD), and N2-sorption analysis. It was confirmed that the hollow silica sphere had a hexagonal structure with a Brunauer-Emmett-Teller (BET) specific area of 1623 ㎡/g.