• 한국분말재료학회지
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• 제17권3호
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• pp.230-234
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• 2010

Homogenous silica-coated $CoFe_2O_4$ samples with controlled silica thickness were synthesized by the reverse microemulsion method. First, 7 nm size cobalt ferrite nanoparticles were prepared by thermal decomposition methods. Hydrophobic cobalt ferrites were coated with controlled $SiO_2$ using polyoxyethylene(5)nonylphenylether (Igepal) as a surfactant, $NH_4OH$ and tetraethyl orthosilicate (TEOS). The well controlled thickness of the silica shell was found to depend on the reaction time and the amount of surfactant used during production. Thick shell was prepared by increasing reaction time and small amount of surfactant.

• Macromolecular Research
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• 제17권5호
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• pp.307-312
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• 2009

Core-shell hydrogel nanocomposite was fabricated by encapsulating a silica-gold nanoshell (SGNS) with poly(N-isopropylacrylamide-co-acrylic acid) (PNIPAM-co-AAc) copolymer. The oleylamine-functionalized SONS was used as a nanotemplate for the shell-layer growth of hydrogel copolymer. APS (ammonium persulfate) was used as a polymerization initiator to produce a hydrogel-encapsulated SGNS (H-SGNS). The amounts of NIPAM (N-isopropylacrylamide) monomers were optimized to reproduce the hydrogel-encapsulated SGNS. The shell-layer thickness was increased with the increase of polymerization time and no further increase in the shell-layer thickness was clearly observed over 16 h. H-SGNS exhibited the systematic changes of particle size corresponding to the variation of pH and temperature, which was originated from hydrogen-bonding interaction between PNIPAM amide groups and water, as well as electrostatic forces attributed by the ionization of carboxylic groups in acrylic acid.

• 폴리머
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• 제28권6호
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• pp.487-493
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• 2004

계면간 상호작용이 약한 폴리(에틸 아크릴레이트-co-t-부틸 아크릴레이트) (PEB) 에멀션 고분자를 사용한 나노복합체 혼합용액에서는 pH변화에 따라 고분자 입자들과 실리카 나노입자들의 분포 형태가 결정되었다. 이러한 나노복합체는 실리카 입자의 응집이 심하였고 불규칙적인 분산성을 나타내었다. 메타아크릴옥시프로필트리메톡시실란 (MPS)를 사용하여 개질한 용액 중합 고분자나 실리카 나노입자를 사용한 나노복합체에서는 계면간 강한 상호작용으로 인하여 실리카 나노입자가 미세하게 분산되었고 코어-쉘 형태학적 특성을 나타냈다. 계면을 MPS로 개질한 나노복합체에서는 강한 수소 결합 상호작용이 존재하는 것을 적외선 분광계로 확인하였다. 강한 계면 상호작용을 갖는 나노복합체는 고분자 사슬의 유리 전이 온도가 증가하였고 ΔC$_{p}$ 는 감소하였으며 열분해 온도는 상승되었다.며 열분해 온도는 상승되었다.

• 한국재료학회지
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• 제10권6호
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• pp.415-421
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• 2000

실리카 바인더 함량이 지르콘 쉘 주형의 기계적 특성에 미치는 영향을 고찰하였다. 실리카 졸/지르콘 함량비 $R_w$는 0.18~0.43 범위에서 변화시켰으며, 주형의 소결온도는 $871^{\circ}C~1400^{\circ}C$ 범위에서 변화시켰다. 생형의 상온강도는 실리카 졸/지르콘 함량비 $R_w$에 비례하여 증가하였다. 소결온도가 $1300^{\circ}C$ 이하인 경우, $R_w$가 증가함에 따라 소결된 주형의 상온강도와 치밀화는 증가하였다. 그러나 $R_w$가 0.43이고 $1400^{\circ}C$에서 3시간 동안 소결시킨 경우 주형의 상온강도와 치밀화가 오히려 감소하였다. 이는 소결 중 내화물 입자와 실리카 바인더와 열팽창계수의 차이에 기인하는 것으로 판단된다. 정밀주조용 지르콘 쉘 주형 제작을 의한 최적의 $R_w$ 값은 0.33인 것으로 나타났다.

• 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.

• 한국연초학회지
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• 제16권2호
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• pp.181-190
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• 1994

Various active carbons were made from plant sources of coconut shell, pine tree, oak tree and lignite coal. Pore characteristics of these adsorbents were investigated. 1, With increasing activation time, specific surface area and pore volume increased, but the development of micropores was limited at a certain level. The average pore diameter, by BET, of coconut active carbon was 15.5-21.8$\AA$ and that of lignite carbon was 15.6-31.3$\AA$. The pore diameters of silica-gel, sepiolite and zeolite was 30.9$\AA$, 58.6$\AA$ and 55.7$\AA$, respectively. 2. The Horvath - Kawazoe micropore diameter of coconut shell active carbon was under 10.5$\AA$ and that of the other active carbon was under 20.9$\AA$ but silica-gel 33$\AA$, sepiolite 103 $\AA$ and zeolite was unexpectedly large to be 175$\AA$. From the difference between BET micropore diameter and Howath - Kawazoe diameter, it could be said that silica - gel has comparatively uniform pore diameter but sepiolite and zeolite have very uneven diameter. 3. Total pore volume of coconut shell active carbon was 0.27-1.04 cm3/g but that of the other active carbon, 0.23-0.62 cm3/g, was much lower than that of coconut shell active carbon. Hydrophilic adsorbent silica - gel and sepiolite showed big difference in specific surface area, but pore volumes of these were 0.47 and 0.56 cm3/g showing similar value and micropore volumes of these were, respectively, 0.06 cm3/g and 0.04 cm3/g. Total pore volume of zeolite was 0.1 cm3/g and that of micropore was only 0.02 cm3/g.

• 산업기술연구
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• 제23권A호
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• pp.199-206
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• 2003

The charcoal-encapsulated methyl silica microcapsules were prepared by a O/W microemulsion sol-gel method, and the adsorption properties on aquatic humic acid were investigated. The capsules prepared were spherical, $100{\sim}1000{\mu}m$ in size. The size distribution was controllable by adjusting the size of charcoal powder, charcoal/methyl silica ratio, and agitating speed in O/W sol-gel process. Adsorption efficiency of charcoal for aquatic humic acid was decreased after encapsulation by methyl silica shell. The decreased adsorption efficiency can be dependent on the decrease of the BET surface area and pore volume after encapsulation. Diffusion properties of humic acid through the capsule shell also played an important role on adsorption efficiency. Therefore, the reasonable target pollutants for the capsules can be VOC or odor molecules which can overcome diffusion barrier through shell of capsules in air condition. Functionalization methods for the charcoal-encapsulated $CH_3(SiO)_n$ microcapsules by incorporation of $TiO_3$ as a phtocatalytic function and by incorporation of inorganic pigment as a color function were also investigated. $TiO_2$ coating properties were controllable by adjusting pH, temperature, and the concentration of $TiOSO_4$. In XRD measurement, the crystal form of the coated $TiO_2$ was anatase. For the colorization of the capsules, inorganic pigments were more efficient than organic dyes, and various color was introduced to the capsules using inorganic pigments.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.553-553
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• 2012

The artificial shells of hard inorganic nanocomposites on individual cells would protect the cells physically and chemically, and control cell division. These emerging properties could be combined with cell-surface functionalizations for applications to cell-based sensors and assays as well as for fundamental studies on single-cell biology. In this work, individual Chlorella cells were encapsulated within a silica/titania nanocomposite shell in a biocompatible fashion that utilized a designed peptide, RKKRKKRKKRKKDDDDDDDD, as a catalytic template for formation of both $SiO_2$ and $TiO_2$ on the cell surface. The cell viability was maintained, and the division of the encapsulated Chlorella cells was controlled. The cell viability was enhanced compared with the $TiO_2$-shell formation. In addition, the incorporation of $TiO_2$ to the shell made it possible to anchor the ligands of interest to the shell via catechol chemistry. All in all, the combination of biological $SiO_2$ and abiolgical $TiO_2$ for the shell formation gave more tunability of the artificial shells compared with the $SiO_2$ or $TiO_2$ shells only.

• 박물관보존과학
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• 제27권
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• pp.91-102
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• 2022

철기 문화재 복원에 사용되고 있는 실리카 계열의 무기질 충전제는 열팽창률감소, 흐름성 개선 등의 기능성 부여를 목적으로 사용되고 있다. 그러나 충전제의 양이 많을 수록 복원재의 물성저하 및 황변 현상 촉진의 원인이되며, 결과적으로 재처리로 이어져 유물의 피로도를 상승시키는 결과를 초래한다. 따라서 복원제와 충전제의 혼합 정량화 및 황변성 연구 필요성이 강조될 수 밖에 없다. 이를 보완하기 위해 실리카계 경량 충전제인 Micro Shell을 비교군으로 물성연구를 진행하였다. 실험 결과 기존에 사용하던 충전제에 비해 Micro Shell이 황변도 발생 수치가 최대 34% 낮았으며, 충전제의 배합양에 따라서 공통적으로 접착력과 비중의 물성 수치값이 좋은 것을 확인하였다. 본 연구 결과 Micro Shell의 사용 가능성에 대해 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제32권10호
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• pp.3707-3711
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• 2011

Silver nanoparticles coated with silica can be obtained by the reduction of $AgNO_3$ with hydrazine in the presence of NaOH-stabilized, active silicic acid (polysilicic acid). The size of the silver nanoparticles and the silica shell thicknesses were affected by varying the hydrazine content, the active silicic acid content and the experimental method (e.g. hydrothermal method). Typically, silver nanoparticles sized around 40 nm were aggregated, connected by silica. The presence of peaks centered around 400 nm in UV-vis spectra corresponds to the surface plasmon resonance of silver nanoparticles. The size of the aggregated silver nanoparticles increased with increasing hydrazine concentration. Under hydrothermal conditions at $150^{\circ}C$ the formation of individual silica particles was observed and the sizes of the silver nanoparticles were reduced. The hydrothermal treatment of silver nanoparticles at $180^{\circ}C$ gives a well-defined Ag@$SiO_2$ core-shell in aggregated silica sol particles. The absorption band observed at around 412 nm were red-shifted with respect to the uncoated silver nanoparticles (${\lambda}_{max}$ = 399 nm) due to the larger refractive index of silica compared to that of water. The formation of silver nanoparticles coated with silica is confirmed by UV-visible absorption spectra, transmission electron microscopy (TEM) and energy-dispersive spectroscopy (EDS) data.