• 한국세라믹학회지
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• 제54권3호
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• pp.222-227
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• 2017

Flake-type micro hollow silica was synthesized by precipitation method using an $Mg(OH)_2$ inorganic template and sodium silicate and ammonium sulfate as the silica precursors. We investigated the effects of the silica precursor concentration on the shape, shell thickness, and surface of the hollow silica. When the concentration of the silica precursor was 0.5 M, the hollow silica had a smooth and translucent thin shell, but the shell was broken. On the other hand, the shell thickness of the hollow silica changed in the range of 12 nm to 18 nm with the increase of the precursor concentration from 0.7 M to 1.1 M. Simultaneously, unintended spherical silica satellites were created on the shell surface. The number of satellites and the size rose according to the increased concentration of silica precursor. The reason for the formation of spherical silica satellites is that the $NH_4OH$ nucleus generated in the synthesis of hollow silica acted as another silica reaction site.

• Bulletin of the Korean Chemical Society
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• 제32권8호
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• pp.2683-2688
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• 2011

Silica-manganese oxides with a core-shell structure were synthesized via precipitation of manganese oxides on the $SiO_2$ core while varying the concentration of a precipitation agent. Elemental analysis, crystalline property investigation, and morphology observations using low- and high-resolution electron microscopes were applied to the synthesized silica-manganese oxides with the core-shell structure. As the concentration of the precipitating agent increased, the manganese oxide shells around the $SiO_2$ core sequentially appeared as $Mn_3O_4$ particles, $Mn_2O_3+Mn_3O_4$ thin layers, and ${\alpha}-MnO_2$ urchin-like phases. The prepared samples were assembled as electrodes in a supercapacitor with 0.1 M $Na_2SO_4$ electrolyte, and their electrochemical properties were examined using cyclic voltammetry and charge-discharge cycling. The maximum specific capacitance obtained was 197 F $g^{-1}$ for the $SiO_2-MnO_2$ electrode due to the higher electronic conductivity of the $MnO_2$ shell compared to those of the $Mn_2O_3$ and $Mn_3O_4$ phases.

• Macromolecular Research
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• 제16권5호
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• pp.399-403
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• 2008

Monodisperse, micron-sized, hybrid particles having a core-shell structure were prepared by coating the surface of poly(methyl methacrylate)(PMMA) microspheres with silica and by copolymerizing acrylamide (AAm) to supply the hydrogen bonding effect by means of the amide groups. Tetraethoxysilane (TEOS) was then slowly dropped onto the medium under certain conditions. Because of the hydrogen bonding between the amide of the PMMA particles and the hydroxyl group of the hydrolyzed silanol, a silica shell was generated on the PMMA core particles. The morphology of the hybrid particles was investigated with transmission (TEM) and scanning (SEM) electron microscopy as a function of the medium conditions and the amount of TEOS. Improved thermal properties were observed by TGA analysis.

• 대한화학회지
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• 제56권4호
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• pp.478-483
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• 2012

We successfully synthesized $Fe_3O_4/SiO_2$ nanoparticles with ultrathin silica layer of $1.0{\pm}0.5$ nm that was fine controlled by changing concentration of $Fe_3O_4$. Among various reaction conditions for silica coating, increasing concentration of $Fe_3O_4$ was more effective approach to decrease silica thickness compared to water-to-surfactant ratio control. Moreover, we found that concentration of the 1-octanol is also important factor to produce the homogeneous $Fe_3O_4/SiO_2$ nanoparticles. The present approach could be available to apply on preparation of other core/shell nanoparticles with ultrathin silica layer.

• Elastomers and Composites
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• 제45권1호
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• pp.7-11
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• 2010

본 논문에서는 polyethyleneimine (PEI)를 커플링제로 사용하여 간단한 공정을 통하여 아세틸렌 블랙/실리카 복합체 입자를 제조하였다. 복합체 입자는 PEI를 아세틸렌 블랙 표면에 흡착시키고 졸-겔 합성공정을 통하여 실리카를 아세틸렌 블랙 위에서 합성하는 두단계 공정을 통하여 제조되었다. 복합체 입자의 모폴로지 분석 결과 실리카가 아세틸렌 블랙위에 존재하는 core-shell 구조를 확인하였으며, 표면에 상당한 미세기공이 존재함을 알 수 있었다.

• 한국결정성장학회지
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• 제6권4호
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• pp.521-531
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• 1996

분무건조법을 이용하여 무기질막 microcapsule과 무기질/유기질막 microcapsule을 제조하였다. 무기질막 microcapsule은 core 물질로 $K_{4}SO$와 clay shell 물질로 colloidal silica를 사용하였고, 무기질/유기질막 microcapsule은 core 물질로 상기 제조된 무기질막 microcapsule을 shell 물질로는 ethyl cellulose를 사용하여 각각의 microcapsule를 제조하였다. 제조된 microcapsule이 기능성을 갖기 위하여는 구형의 균일한 표면과 세공용적이 매우 중요하다. 무기질막 microcapsule인 경우 core/shell의 체적비가 0.3/0.7인 경우 구형의 균일한 표면의 microcapsule이 제조되었으며, 무기질/유기질막 microcapsule인 경우, 무게비가 0.76/0.24일 때 균일한 표면을 갖는 microcapsule이 제조되었다. 무기질/유기질막 microcapsule인 경우, 무기질막 microcapsule보다 세공용적이 감소하였고, shell물질(ethyl cellulose)의 양이 증가할수록 피복이 균일하게 되며, 세공용적도 감소하였다.

• 폴리머
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• 제33권5호
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• pp.452-457
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• 2009

다중벽 탄소나노튜브 및 전도성 고분자인 PEDOT으로 이루어진 하이브리드 나노재료를 제조하였다. 다중벽 탄소나노튜브 표면에 처리반응을 수행함으로써 -Br 특성기를 갖는 다중벽 탄소나노튜브를 제조하였으며, 이를 중합반응의 개시제로 사용하였다. 이와 함께 MMA를 사용하여 촉매와 리간드 존재 하에서 원자이동 라디칼중합 공정을 수행함으로써 다중벽 탄소나노튜브 표면에 PMMA가 공유결합된 나노복합체를 제조하였다. 미니에멀젼 중합공정을 통하여 제조된 PS 수용성 에멀젼에 EDOT과 산화가를 투입하여 산화중합을 수행함으로써 core-shell 구조를 갖는 PEDOT/PS 나노입자를 제조하였다. 실란화합물로 표면 처리한 silica 입자를 PEDOT:poly(styrene sulfonate) (PSS) 수용성 분산액에 투입한 후 표면화학 반응과정을 수행함으로써 silica 외벽에 PEDOT:PSS가 코팅된 나노입자를 제조하였다. 하이브리드 나노재료들은 TEM, FE-SEM, TGA, EDX, UV 그리고 FT-IR 등을 사용하여 분석되었다.

• Smart Structures and Systems
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• 제25권3호
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• pp.337-343
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• 2020

In this paper, we focused on the self-healing concrete using new nano-capsules. Three types of nano-capsules with respect to availability, high strength and temperature tolerance are used; type 1 is URF and polyethylene (PE) as shell and nano titanium oxide (TiO₂) as core, type 2 is URF and PE as shell and nano silica oxide (SiO₂) as core, type 3 is PE as shell and nano silica oxide (SiO₂) as core. The concrete samples mixed by nano-capsules with three percents of 0.5, 1 and 1.5. Based on experimental tests and the compressive strength of samples, the URF-PE-SiO₂ is selected for additional tests of compressive strength before and after recovery, ultrasonic test, ion chlorine and water penetration depths. After careful investigation, it is concluded that the optimum value of URF-PE-SiO₂ nano-capsules is 0.5% since leads to higher compressive strength, ultrasonic test, ion chlorine and water penetration depths.

• KEPCO Journal on Electric Power and Energy
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• 제7권1호
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• pp.167-169
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• 2021

In this study, monodispersive silica nanoparticles with double mesoporous shells were synthesized, and the pore size of synthetic mesoporous silica nanoparticles was controlled. Cetyltrimethylammonium chloride (CTAC), N, N-dimethylbenzene, and decane were used as soft template and induced to form outer mesoporous shell. The resultant double mesoporous silica nanoparticles were consisted of two layers of shells having different pore sizes, and it has been confirmed that outer shells with larger pores (Mean pore size > 2.5 nm) are formed directly on the surface of the smaller pore sized shell (Mean pore size < 2.5 nm). It was confirmed that the regulation of the molar ratio of pore expansion agents plays a key role in determining the pore size of double mesoporous shells.

• Bulletin of the Korean Chemical Society
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• 제26권2호
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• pp.227-228
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• 2005