• Advances in nano research
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• 제6권1호
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• pp.1-19
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• 2018

Iron oxide nanoparticles excite researcher interest in biomedical applications due to their low cost, biocompatibility and superparamagnetism properties. Magnetic iron oxide especially magnetite ($Fe_3O_4$) possessed a superparamagnetic behaviour at certain nanosize which beneficial for drug and gene delivery, diagnosis and imaging. The properties of nanoparticles mainly depend on their synthesis procedure. There has been a massive effort in developing the best synthetic strategies to yield appropriate physico-chemical properties namely co-precipitation, thermal decomposition, microemulsions, hydrothermal and sol-gel. In this review, it is discovered that magnetite nanoparticles are best yielded by co-precipitation method owing to their simplicity and large production. However, its magnetic saturation is within range of 70-80 emu/g which is lower than thermal decomposition and hydrothermal methods (80-90 emu/g) at 100 nm. Dimension wise, less than 100 nm is produced by co-precipitation method at $70^{\circ}C-80^{\circ}C$ while thermal decomposition and hydrothermal methods could produce less than 50 nm but at very high temperature ranging between $200^{\circ}C$ and $300^{\circ}C$. Thus, co-precipitation is the optimum method for pre-compliance magnetite nanoparticles preparation (e.g., 100 nm is fit enough for biomedical applications) since thermal decomposition and hydrothermal required more sophisticated facilities.

• 한국결정성장학회지
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• 제11권5호
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• pp.185-189
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• 2001

비정질 인산알루미늄 분말은 화학양론조성비의 $Al_2(SO_4)_3$와 $H_3PO_4$혼합물을 NaOH 또는 KOH 용액을 이용하여 중화 반응시킨 뒤 이를 수열침전법에 의해 단일상으로 얻을 수 있었으며, 합성조건은 다음과 같다. 즉, 출발원료; $Al_2(SO_4)_3$와 $H_3PO_4$, 중화반응의 pH범위; 5.6~6.0, 수열반응의 온도범위; 170~$180^{\circ}C$, 수열반응의 시간범위; 4~5시간이었다. 이와 같은 조건하에서 얻어진 생성물은 0.1~0.3$\mu\textrm{m}$ 크기의 비정질 인산알루미늄 미립자였으며 그리고 미국약전에 따라 실험한 결과 모두 적합하였다.

• 한국결정성장학회지
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• 제19권5호
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• pp.223-227
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• 2009

침전법, 수열 반응법, 리간드 보조법을 사용하여 다양한 형태의 $BaCO_3$ 결정을 합성하였다. 수용액에서 $Ba(NO_3)_2$과 $Na_2CO_3$를 단순 침전시키면 불규칙한 입자 형태의 $BaCO_3$ 마이크로 결정이 얻어졌다. 수열 반응으로 $Ba(NO_3)_2$와 urea를 반응시켜 육각형 막대 피라미드 형태의 $BaCO_3$를 합성하였으며, 리간드 보조 수열 반응법을 사용하여 육각형 막대형의 $BaCO_3$를 합성하였다. 리간드 농도가 증가 할수록 $BaCO_3$ 육각형 막대의 종횡비가 증가하였다.

• 한국결정성장학회지
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• 제26권3호
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• pp.95-100
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• 2016

본 연구에서는 염화주석, 하이드라진 그리고 수산화나트륨을 원료로 하여 용액환원침전법과 수열반응법을 이용하여 주석산화물 결정을 제조하여, 주요 실험 변수에 의한 결정상 및 형상을 XRD와 SEM을 이용하여 분석하였다. 원료의 몰 비에 따라 구형 및 판상의 주석산화물 결정을 얻을 수 있었으며, 그 결정상은 SnO, $Sn_6O_4(OH)_4$이었다. 그리고 수열반응법에 의하여 얻어진 결정 모양은 온도 조건에 따라 판상 및 꽃 모양의 SnO 결정이 얻어졌다.

• Korean Chemical Engineering Research
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• 제50권5호
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• pp.808-814
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• 2012

수열합성법을 이용하여 zinc acetate와 암모니아수를 $80^{\circ}C$의 고온에서 침전 반응시켜 광촉매용 산화아연 입자를 제조하였다. 암모니아수의 pH, 전구체인 zinc acetate의 농도 변화가 산화아연 입자의 특성에 미치는 영향을 조사하였다. 암모니아수 pH 11, zinc acetate의 농도 1.0M, 침전반응온도 $80^{\circ}C$의 조건에서 제조된 산화아연이 평균 입경 $3{\mu}m$로 가장 작았으며, SEM과 XRD 분석을 통하여 육방정계의 봉상 막대형, Anatase 형태의 산화아연이 제조됨을 확인할 수 있었다. DRS와 PL 분석을 통하여 제조된 산화아연이 200~400 nm의 자외선 영역에서 활성을 나타냄을 확인하였고, 자외선 조사 하에서 광분해 실험을 수행한 결과 산화아연은 3시간 동안 식용색소인 Brilliant blue FCF를 57%까지 분해할 수 있었다.

• 한국분말재료학회지
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• 제18권6호
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• pp.546-551
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• 2011

Ag spot-coated Cu nanopowders were synthesized by a hydrothermal-attachment method (HA) using oleic acid capped Ag hydrosol. Cu nano powders were synthesized by pulsed wire exploding method using 0.4 mm in diameter of Cu wire (purity 99.9%). Synthesized Cu nano powders are seen with comparatively spherical shape having range in 50 nm to 150 nm in diameter. The oleic acid capped Ag hydrosol was synthesized by the precipitation-redispersion method. Oleic acid capped Ag nano particles showed the narrow size distribution and their particle size were less than 20 nm in diameter. In the case of nano Ag-spot coated Cu powders, nanosized Ag particles were adhered in the copper surface by HAA method. The components of C, O and Ag were distributed on the surface of copper powder.

• 한국분말재료학회지
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• 제19권6호
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• pp.424-428
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• 2012

Nano Pd spot-coated active carbon powders were synthesized by a hydrothermal-attachment method (HAA) using PVP capped Pd colloid in a high pressure bomb at $250^{\circ}C$, 450 psi, respectively. The PVP capped Pd colloid was synthesized by the precipitation-redispersion method. PVP capped Pd nano particles showed the narrow size distribution and their particle sizes were less than 8nm in diameter. In the case of nano Pd-spot coated active carbon powders, nano-sized Pd particles were adhered in the active carbon powder surface by HAA method. The component of Pd was homogeneously distributed on the active carbon surface.

• 한국재료학회지
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• 제21권8호
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• pp.425-431
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• 2011

The industrial manufacturing of YSZ products can be summarized as a three step process: a) hydrolysis of zirconyl chloride and mixing of other solutions, b) precipitation, and c) calcination. The addition of ammonia or OH- is essential in the precipitation process. However, a strong agglomeration was observed in the results of an ammonia or OH- addition. Thus, it is necessary to disperse the powders smoothly in order to improve the mechanical strength of YSZ. In this study, YSZ was synthesized using the urea stabilizer and hydrothermal method. YSZ powders were synthesized using a hydrothermal method with Teflon Vessels at $180^{\circ}C$ for 24 h. The mole ratio of urea to Zr was 0, 0.5, 1, and 2. The crystal phase, particle size, and morphologies were analyzed. Rectangular specimens ($33\;mm{\times}8\;mm{\times}1{\pm}0.5\;mm$) for three-point bend tests were used in the mechanical properties evaluation. The crystalline of YSZ powders observed a tetragonal phase in the sample with a ratio of Zr:urea = 1:2 addition and a hydrothermal reaction time of 24 h. The average primary particle size of YSZ was measured to be 9 nm to 11 nm. The agglomerated particle size was measured from 15 nm to 30 nm. The three-point bending strength of the YSZ samples was 142.47 MPa, which is the highest value obtained for the Zr:urea = 1:2 ratio addition YSZ sample.

• Bulletin of the Korean Chemical Society
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• 제20권8호
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• pp.869-874
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• 1999

In this paper, electrochemical techniques are used to investigate hydrothermal-electrochemically formation of barium titanate (BT) ceramic films. For comparison, the electrochemical behaviors of anodic titanium oxide films formed in alkaline solution were also investigated both at room temperature and in hydrothermal condition at 150.0 ℃. Film structure and morphology were identified by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Titanium oxide films produced at different potentials exhibit different film morphology. The breakdown of titanium oxide films anodic growth on Ti electrode plays an important roles in the formation of BT films. BT films can grow on anodic oxide/metal substrate interface by short-circuit path, and the dissolution-precipitation processes on the ceramic film/solution interface control the film structure and morphology. Based upon the current experimental results and our previous work, extensively schematic proce-dures are proposed to model the mechanism of ceramic film formation by hydrothermal-electrochemical method.

• Korean Chemical Engineering Research
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• 제49권6호
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• pp.752-757
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• 2011

암모니아수와 zinc acetate로부터 액상 수열합성법에 의한 ZnO의 제조에 있어 반응온도, 반응물의 농도와 혼합방법, 용액의 pH 등 반응조건에 따른 ZnO 입자의 형상과 입자분포 등 제조특성을 고찰하고, UV 조사하에 tartrazine의 광분해를 측정하여 합성된 ZnO의 광촉매로서의 성능을 확인하였다. 반응용액의 pH가 높을수록 ZnO 입자의 평균 크기는 증가하였고, zinc acetate의 농도가 증가할수록 그리고 반응온도가 증가할수록 입자의 크기는 감소하였다. 반응용액의 혼합시 암모니아수 주입 후에 zinc acetate를 첨가하였을 경우 더 작은 입자를 얻을 수 있었다. 최소 크기의 ZnO 입자의 생성을 위한 최적 조건은 용액의 pH 11.2, zinc acetate의 농도 0.6 M, 반응온도 $90^{\circ}C$였으며, 입자 평균크기는 3.133 ${\mu}$m이었다. 합성온도 $80^{\circ}C$, zinc acetate 농도 1.0M 및 반응용액의 pH 11.2의 조건에서 합성된 ZnO에 의한 tartrazine의 광촉매 분해는 분해시간 60분에서 약 97%의 분해율을 보였다.