• Title/Summary/Keyword: 용액합성

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Preparation of Magnetic Chitosan Microsphere Particles (나노 크기의 마그네타이트 입자를 이용한 자성 키토산 미소구체의 제조)

  • Ko, Sang-Gil;Cho, Jun-Hee;Ahn, Yang-Kyu;Song, Ki-Chang;Choi, Eun-Jung
    • Journal of the Korean Magnetics Society
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    • v.16 no.1
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    • pp.66-70
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    • 2006
  • Magnetite nanoparticles, which have been extensively used in many fields, were encapsulated with a natural polymer, chitosan, to improve their biocompatibility. We have synthesized magnetite $(Fe_3C_4)$ nanoparticles using chemical coprecipitation technique with sodium oleate as surfactant. Nanoparticle size can be varied from 1.2 to 7.4nm by controlling the sodium oleate concentration. Magnetite phase nanoparticles could be observed from X-ray diffraction. Magnetic colloid suspensions containing particles with sodium oleate and chitosan have been prepared. High magnetic property chitosan-microsphere particles were prepared from oleate-coated magnetite suspension using spray method. The surftce, and tile morphology of the magnetic chitosan microsphere particles were characterized using optical microscope and scanning electron microscope. Magnetic hysteresis measurement were performed using a superconducting quantum interference device (SQUID) magnetometer at room temperature to investigate the magnetic properties of the chitosan microspheres including magnetite nanoparticles. The SQUID measurements revealed superparamagnetism of nanoparticles.

Preparation and Characterization of BaTiO3 Powders and Thin films (티탄산바륨 분말과 박막의 제조 및 특성 연구)

  • Jung, Miewon;Son, Hyunjin;Lee, Jiyun;Kim, Hyunjung
    • Analytical Science and Technology
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    • v.17 no.2
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    • pp.173-179
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    • 2004
  • The $BaTiO_3$ powders and thin films were prepared by an alkoxide modified sol-gel process (polymerization-complex route) using ethylene glycol. The stable starting (Ba-Ti)-mixed metal organic sol was made by addition of acetylacetone. The $BaTiO_3$ powders, which had a particle size of 40~77 nm, were crystallized from an amorphous to a tetragonal phase on annealing at 700 and $1100^{\circ}C$ for 1 h. From FT-IR, solid-state $^{13}C$ CP/MAS NMR spectroscopy and X-ray diffractometry, the trace of the Ba-Ti-oxycarbonate phase first appeared at $400^{\circ}C$. Hydrolyzed sol was spin coated on a quartz wafer at 3500 rpm for 60 s and pyrolyzed at $1100^{\circ}C$ for 1 h. After heat treatment, the coated layer became dense and smooth.

A Study on the Cementation of Cu, Ni and Co Ions with Mn Powders in Chloride Solution (염산용액중에서 망간분말에 의한 구리, 니켈 및 코발트 이온의 세멘테이션에 관한 연구)

  • 안재우;안종관;박경호
    • Resources Recycling
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    • v.9 no.3
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    • pp.3-12
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    • 2000
  • A Study on the cementation for the recovery of Cu, Ni and Co with Mn metallic powders in leaching solution from the manganese nodule that have removed Fe ions was studied. The results showed that the recovery efficiencies of metal ions with Mn powders increased when the temperature, pH and the concentration of chloride ions were increased in mixed solution. And the recovery efficiencies of Cu was 98% and not changed with the addition amounts of Mn powders but, in case of Co and Ni, the recovery efficiencies were increased with the addition amounts. The particle size of precipitate was about $5\mu\textrm{m}$. From the results of experiment we proposed the two-step cementation process for the recovery of Cu, Ni and Co with Mn powders.

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Platinum Nanoparticles Synthesis using Recovered Platinum from Waste Fuel cell (폐연료전지(廢燃料電池)스택으로부터 회수(回收)된 백금(白金)의 나노 입자(粒子) 제조(製造))

  • Kim, Young-Ae;Kwon, Hyun-Ji;Koo, Jeong-Boon;Kwak, In-Seob;Sin, Jang-Sik
    • Resources Recycling
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    • v.20 no.2
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    • pp.67-73
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    • 2011
  • In this study, for recovery of renewable noble metal from used stack of fuel cell, synthesis of platinum nano particle is established through effect of platinum solution concentration, pH value, reducing agent and dispersing agent at a volume ratio of 1 mM $H_2PtCl_6$:10 mM $NaBH_4$:8 mM Cl4TABr = 1:0.4:0.4(vol.%), pH4, $50^{\circ}C$, 160 rpm and 10min. Less than 5 nm platinum particles were synthesized using Pt leaching solution from used MEA of stack under same condition of method using simulated Pt solution. The characteristics of synthesized nano particles was illustrated by XPS analysis as the reduction of platinum ions into platinum metals(zero-valent).

Synthesis parameters of hydroxyapatite preparation by a precipitation process (합성조건이 침전법에 의한 Hydroxyapatite 제조에 미치는 영향)

  • Moon, Sung Wook;Lee, Byeong Woo
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.32 no.3
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    • pp.96-102
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    • 2022
  • Hydroxyapatite (HAp) was synthesized from calcium hydroxide (Ca(OH)2) reacting with phosphoric acid (H3PO4) in aqueous solution. HAp powders were synthesized from extremely high concentration of precursor solutions over 3 M of Ca(OH)2 aqueous suspension using modified process parameters such as phosphoric acid (H3PO4) pouring rate, aging time and post ball milling process. Regardless of phosphoric acid pouring rate, the DCPD (dicalcium phosphate dihydrate) was formed at room temperature and when heated above 700℃, β-TCP (tricalcium phosphate) was synthesized and the amount reached its maximum at 900℃. When the synthesized powder was sintered at 1150℃, β-TCP, a high temperature impurity phase, remained. The single HAp phase without DCPD was obtained from post ball-milled precipitates followed by 3 day aging. For the ball-milled precipitates even without the aging process, the desired single HAp phase without β-TCP could be obtained by heat treatment above 500℃. The post ball milling process provided a convenient route for HAp synthesis.

액상법에 의한 단분산 ZnS입자 및 피복형복합입자의 합성

  • 김영도;신건철
    • Proceedings of the Korea Association of Crystal Growth Conference
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    • 1997.10a
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    • pp.27-31
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    • 1997
  • 액상법에 의한 단분산 ZnS입자의 합성을 60~9$0^{\circ}C$에서 행하여, 반응조건이 ZnS입자의 형태에 미치는 효과를 검토했다. ZnS입자의 형태는 반응 시간의 경과와 더불어 단분산으로부터 다분산 혹은 응집체로 변화하였다. 반응 온도 60~9$0^{\circ}C$에서 초기 농도적이 중간값이고, 반응시간이 짧을 경우 입경 0.2~0.8$\mu\textrm{m}$의 구상 단분산 입자를 얻었다. 또한 Ag$_2$NO$_3$, EtOH용액, $0^{\circ}C$에서, Ag$_2$S에 의한 ZnS의 균일 피복이 가능하였다.

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The characteristic evaluation of gelatin/Ag nanoparticles biocomposite prepared by solution plasma process (유체 플라즈마 공정으로 제조 된 젤라틴/은 나노입자 생체복합체의 특성 평가)

  • Kim, Seong-Cheol;Kim, Seong-Min;Kim, Jeong-Wan;Lee, Sang-Yul
    • Proceedings of the Korean Institute of Surface Engineering Conference
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    • 2013.05a
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    • pp.166-166
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    • 2013
  • 유체 플라즈마 공정은 금속 나노입자를 제조하는데 있어서 혁신적이고 친환경적인 공정 방법의 하나이다. 본 연구에서는 유체 플라즈마 공정을 통해 젤라틴 기지재 내에 은 나노입자를 합성하였고, 합성 된 용액은 동결건조를 통해 3D scaffold 형태의 생체복합체로 제조하였다. 이렇게 제조된 생체복합체의 물리적 특성 및 생물학적 특성 평가를 통해 생체복합체의 효율성과 항균 효과가 뛰어남을 확인하였다.

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TiO2 nanostructures by Hydrothermal method : synthesis and properties (수열 합성법에 의한 TiO2 nanotube의 제조 및 특성)

  • Son, Ji-Eun;Jo, Seong-Hun;Lee, Su-Wan
    • Proceedings of the Korean Institute of Surface Engineering Conference
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    • 2014.11a
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    • pp.263-263
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    • 2014
  • 자외선 영역에서 우수한 광촉매 반도체인 이산화티탄($TiO_2$)은 환경, 에너지와 같은 분야 등에 유용하게 이용된다. 용액상에서 고활성 광촉매의 제조가 가능한 수열합성법에 의해 균일한 결정상의 나노 크기의 미세한 이산화티탄($TiO_2$) 입자를 제조하고, XRD, TEM, UV-vis-DRS, 그리고 염료의 광촉매 흡착 반응을 통하여 그 특성과 광촉매 효율을 조사하였다.

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MICROSTURCTURE AND MAGNETIC PROPERTY OF NiZn-FERRITE POWDER SYNTHESIZED BY ULTRASONIC SPRAY PYROLYSIS PROCESS (초음파 분무 열분해법으로 합성한 NiZn 페라이트 분말의 미세구조 및 자기 특성)

  • 남중희;김민상;박상진;김효태;정상진
    • Proceedings of the Korean Magnestics Society Conference
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    • 2002.12a
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    • pp.114-115
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    • 2002
  • 다성분계 세라믹스에 대하여 초미립 및 나노 분말을 제조하기 위해 공침법, 비정질 citrate법, 무기 금속염을 이용한 sol-gel법, 분무 열분해법 등과 같이 비교적 단순한 공정이면서 입도 분포가 좁고 재현성이 우수한 구형의 초미립 또는 나노 분말의 제조에 적합한 방법들이 많이 연구되고있다[1-3]. 분무 열분해법은 출발물질로 용액을 사용하고 미세한 액적(droplet)을 초음파 분무 후 열분해 하여 분말을 합성하는 방법으로, 입자의 조성이 균질하고 구형의 형상을 갖는 우수한 결정상을 얻을 수 있다. (중략)

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Single Crystal Growing of NaX Zeolite Continuos Crystallization (연속결정화에 의한 NaX 제올라이트 단결정 성장)

  • 하종필;서동남;김익진
    • Proceedings of the KAIS Fall Conference
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    • 2000.10a
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    • pp.178-180
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    • 2000
  • 제올라이트의 결정성장은 유도기와 결정성장기 안정화기의 3단계로 진행한다 이러한 제올라이트의 결정성장 기구를 이해하고 결정의 성장기를 계속적으로 연장함으로서 조대한 NaX 제올라이트 결정의 성장을 유도하였으며, 선형결정성장속도에 대하여 고찰하였다. NaX 제올라이트의 수열합성 과정 중 결정성장기에 일정하게 3일 간격으로 반응용액내의 액상을 분리하고 반응겔을 보충하여 제올라이트의 합성 반응이 안정화기로 진행하는 것을 억제하고 결정 성장기를 연장하여 30㎛ 이상의 NaX 제올라이트 결정을 얻었다.