• Title/Summary/Keyword: Spherical silica

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Synthesis of Core-Shell Silica Nanoparticles with Hierarchically Bimodal Pore Structures

  • Yun, Seok-Bon;Park, Dae-Geun;Yun, Wan-Su
    • Proceedings of the Korean Vacuum Society Conference
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    • 2011.02a
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    • pp.467-467
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    • 2011
  • Reflecting the growing importance of nanomaterials in science and technology, controlling the porosity combined with well-defined structural properties has been an ever-demanding pursuit in the related fields of frontier researches. A number of reports have focused on the synthesis of various nanoporous materials so far and, recently, the nanomaterials with multimodal porosity are getting an emerging importance due to their improved material properties compared with the mono porous materials. However, most of those materials are obtained in bulk phases while the spherical nanoparticles are one of the most practical platforms in a great number of applications. Here, we report on the synthesis of the core-shell silica nanoparticles with double mesoporous shells (DMSs). The DMS nsnoparticles are spherical and monodispersive and have two different mesoporous shells, i.e., the bimodal porosity. It is the first example of the core-shell silica nanoparticles with the different mesopores coexisting in the individual nanoparticles. Furthermore, the carbon and silica hollow capsules were also fabricated via a serial replication process.

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Evaluation and Comparative Physical/Biological Removal Performance for Extremely Low-Concentration NDMA(N-nitrosodimethylamine) (극저농도 NDMA(N-nitrosodimethylamine) 물리적/생물학적 처리 효율 비교 평가)

  • Park, Seyong;Kim, Hui Joo;Kim, Moonil
    • Journal of the Korean GEO-environmental Society
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    • v.12 no.2
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    • pp.55-61
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    • 2011
  • NDMA(N-Nitrosodimethylamine) has been considered as a carcinogenic pollutant even at extremely low-concentration (10ng/L). However, previous researches on NDMA have focused on mainly high concentration due to a difficulty of analysis. In this study, removal efficiencies were evaluated for individual or combined methods with PAC(Powder Activated Carbon), GS(Granular Sludge), MF(Microfiltration), UF(Ultrafiltration) and Silica gel(MCM-41, Diatomite, Spherical silica gel) at both aerobic and anaerobic conditions. Combined method of GS, PAC and UF membrane at anaerobic condition showed the highest removal efficiency of 65% while Silica gel showed the lowest removal efficiency of 6%. The outcomes of this study could be used further study of extremely low-concentration NDMA removal.

Experimental Study in Order to Get the Spherical Particles of Silica Glass by Autogenous Grinding with a Stirred Mill

  • Kotake, Naoya;Toida, Naoyuki;Sato, Yosuke;Kanda, Yoshiteru;Tsubaki, Junichiro;Ishikawa, Tsuyoshi;Nagaoka, Osamu
    • Proceedings of the IEEK Conference
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    • 2001.10a
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    • pp.84-87
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    • 2001
  • A demand for the aggregates is increasing in the field of civil and architectural industry and so on. In these industries, the particle size and shape of aggregates are important factors and especially spherical or rounded particles are desired. In Japan, waste glass is used as one of the aggregate materials for the pavement or the construction. In this study based on the frictional action of material on each other, an autogenous grinding of silica glass with a stirred mill were carried out in order to eliminate flakelike or squarish particles and get spherical or rounded ones for aggregate materials. The autogenous grinding experiments were conducted by applying loads to the particle layer of silica glass. The particle shape was evaluated by the shape index, N/T and the degree of circularity, Ψ$_{ci}$ . The unfractured particles (20~13mm) were evaluated by N/T and Ψ$_{ci}$ , and the products (finer than 10${\mu}{\textrm}{m}$) by Ψ$_{ci}$ . As a result, N/T of the unfractured particles decreased with an increase of grinding time. Ψ$_{ci}$ of the unfractured particles and the products increased with an increase of grinding time (; progress of grinding), and became almost constant in the long time grinding. These tendencies were not changed by the applied load on the particle layer, but the limit value of Ψ$_{ci}$ at the products were varied with the applied load.plied load.

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Preparation of Silica-Gold Composite particles (실리카-골드 복합체의 합성 연구)

  • Kim, Dae-Wook;Shim, Seung-Bo;Chun, Yong-Jin
    • Journal of the Korea Academia-Industrial cooperation Society
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    • v.12 no.11
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    • pp.5365-5369
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    • 2011
  • Silica-gold composite particles were prepared by wet chemical route including impregnation method. The effect of precursor and solvent on the preparation of silica-gold particles was investigated. When spherical silica particles and PVP and hydrogentetrachloroaurate(III) hydrate aqueous solution were used as support material and precursor solution, silica-gold composite particles with light pink color successfully obtained. Obtained composite particles were characterized using FE-SEM, FE-TEM and XRD.

Preparation of Silica Particles by Emulsion-Gel Process Using Membrane Emulsification (막유화 에멀젼-겔 공정에 의한 실리카 입자의 제조)

  • Yeon, Song-Hee;Youm, Kyung-Ho
    • Membrane Journal
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    • v.20 no.2
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    • pp.87-96
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    • 2010
  • We prepared spherical silica particles by controlling various conditions of emulsion-gel procedure using a lab-scale membrane emulsification system equipped with SPG (Shirasu porous glass) membrane having pore size of 2.6 ${\mu}m$. We determined the effects of process parameters of membrane emulsification (dispersed phase pressure, stabilizer and emulsifier concentration in continuous phase, $H_2O$/TEOS ratio, ratio of dispersed phase to continuous phase) on the mean size and size distribution of silica particles. The increase of the dispersed phase pressure and ratio of dispersed phase to continuous phase led to the increase in the mean size of silica particles. On the contrary, the increase in stabilizer and emulsifier concentration and $H_2O$/TEOS ratio caused the reduction of the mean size of particles. Through controlling these parameters, monodisperse spherical silica particles with about 3 ${\mu}m$ of the mean size were finally prepared.

Synthesis of New Black Pigment; Carbon Black Pigment Capsulated into the Meso-pore of Silica as Black Pigment in Cosmetic (새로운 Black Color의 합성;화장품에서 블랙 색소로서 Meso-pore Silca에 캡슐레이션된 Carbon-black Silica)

  • Hye-in, Jang;Kyung-chul, Lee;Hee-chang , Ryoo
    • Journal of the Society of Cosmetic Scientists of Korea
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    • v.30 no.2
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    • pp.189-195
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    • 2004
  • Carbon black have not been used as pigment material in cosmetic because of very low density and dispersity, but carbon black have applicable character as black pigment because of non-toxic, stable physico-chemical property, and black colority. In this study, mesoporous silica samples were synthesized by sol-gel reaction using surfactants-template method; TEOS (tetraethoxysilane) - a) PEO/lecithin, b) PEO/polyethylene glycol, c) lecithin/polyethylene glycol in ethanol/water solution. Synthesized organic-inorganic hybrid - silica were heat-treated in N2 condition at 500$^{\circ}C$. Mesoporous silica with black carbon in pore have the effective density and show the good dispersity in both hydrophilic and hydrophobic solvent. Properties of the samples were measured; specific surface area (750㎡/g) and pore size (4-6nm) using BET, pore structure (cylindrical type) using XRD, morphology (spherical powder with 0.1-0.5$\mu\textrm{m}$ partical size) of the samples using SEM. Carbon-silica black color applied to mascara, it shows a dark black colority and good dispersity as compared with the general black color titania pigment. Moreover, it is possible to control the density of black color pigment because it is possible to control pore volume and particle size of mesoporous silica properly. It show the good volume effects in mascara. That is why possible to apply all kinds of cosmetic products.

Characteristic of Resistance to Tracking and Mechanical Strength by Silica type of Cycloaliphatic-Bisphenol Blending Epoxy (싸이클로알리파틱과 비스페놀 계열 혼합 에폭시 수지의 실리카 종류에 따른 내트래킹 특성 및 기계적 강도)

  • Jung, Hae-Eun;Kang, Han-Young;Park, Seok-Weon;Lee, Jhong-Ho
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2010.06a
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    • pp.90-90
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    • 2010
  • Cycloaliphatic Epoxy와 Bisphenol Epoxy를 각각 mol-wt%비 (80:20, 50:50, 20:80)로 혼합하고 Epoxy Silaned Silica, 바ed Silica, Spherical Silica, ATH(Aluminum Trihydrate)를 충진하여 내트래킹 특성 및 인장강도, 충격강도 등의 기계적 강도를 비교하였다. Cycloaliphatic 수지는 Huntsman사(社)의 CY5622, Bisphenol 수지는 Hexion사(社)E의 Epikote2200을 사용하였으며, Silaned Silica 및 Fused Silica는 Quatzwerke사(社)의 W12, FW12를 사용하였다. 전체 혼합물 중, 에폭시는 약 36%, 실리카는 약 34~540%, ATH는 약 10~30% 이다. 실험결과, ATH 함량이 높은 조성 및 Epoxy Silaned Silica를 사용한 조성과 Cycloaliphatic 혼합비율이 높은 조성이 우수한 내트래킹 특성을 보였다. 또한, Silica의 함량이 증가할수록 기계적 강도가 증가하였으며, Silaned Silica를 사용하였을 때 가장 우수한 특성을 나타내었다. 본 실험의 결과를 통해 옥외용 내트래킹 특성 규격인 IEC60587 4.5kV/6h를 만족하는 조성에 대해 가늠이 가능하였고, 각 조성에 따른 기계적 강도의 확인이 가능하였다.

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Doxorubicin-loaded PEI-silica Nanoparticles for Cancer Therapy

  • Heekyung Park;Seungho Baek;Donghyun Lee
    • Korean Chemical Engineering Research
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    • v.61 no.4
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    • pp.570-575
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    • 2023
  • Targeted anticancer drug delivery systems are needed to enhance therapeutic efficacy by selectively delivering drugs to tumor cells while minimizing off-target effects, improving treatment outcomes and reducing toxicity. In this study, a silica-based nanocarrier capable of targeting drug delivery to cancer cells was developed. First, silica nanoparticles were synthesized by the Stöber method using the surfactant cetyltrimethylammonium bromide (CTAB). Increasing the ratio of EtOH in the solvent produced uniformly spherical silica nanoparticles. Washing the nanoparticles removed unreacted residues, resulting in a non-toxic carrier for drug delivery in cells. Upon surface modification, the pH-responsive polymer, polyethyleneimine (PEI) exhibited slow doxorubicin release at pH 7.4 and accelerated release at pH 5.5. By exploiting this feature, we developed a system capable of targeted drug release in the acidic tumor microenvironment.

Effect of Pore Size of Mesoporous Spherical Silica for the Purification of Paclitaxel from Plant Cell Cultures (식물세포배양으로부터 Paclitaxel 정제를 위한 메조다공성 실리카의 기공크기 영향)

  • Oh, Hyeon-Jeong;Jung, Kyeong Youl;Kim, Jin-Hyun
    • KSBB Journal
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    • v.28 no.3
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    • pp.208-212
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    • 2013
  • Four types of mesoporous spherical silica adsorbents with different physical properties were prepared by spray pyrolysis and were used for the purification of the anticancer agent paclitaxel from plant cell cultures. Pore size had a greater effect on the removal of plant-derived impurities during the pre-purification of paclitaxel compared with surface area and pore volume. An appropriate pore diameter (~9.07 nm) was required to achieve the highest purity (~46.1%) and yield (~82.3%) of paclitaxel. These results were confirmed by HPLC analysis of the absorbent after treatment and Thermogravimetric analysis of the organic substances bonded to the adsorbent.

Preparation of Silica Microgels Using Membrane Emulsification Method (막유화법을 이용한 실리카 마이크로겔의 제조)

  • Youm, Kyung-Ho;Kwak, No-Shin
    • Membrane Journal
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    • v.19 no.2
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    • pp.122-128
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    • 2009
  • We prepared monodispersed spherical silica microgels by controlling various conditions of emulsification procedure using a lab-scale membrane emulsification system equipped with SPG (Shirasu porous glass) porous membrane having pore size of $1.5{\mu}m$. We determined the effects of process parameters of membrane emulsification (ratio of dispersed phase to continuous phase, sodium silicate concentration, emulsifier concentration, dispersed phase pressure, stirring speed) on the mean size and size distribution of silica microgels. The increase of the ratio of dispersed phase to continuous phase, dispersed phase pressure and sodium silicate concentration led to the increase in the mean size of microgels. On the contrary, the increase in emulsifier concentration and stirring speed of the continuous phase caused the reduction of the mean size of microgels. Through controlling these parameters, monodisperse spherical silica microgels with about $6{\mu}m$ of the mean size were finally prepared.