• Title/Summary/Keyword: 용액합성

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A Study for Crystal Growth Inhibition of Ettringite by Solution Synthesis Experiment (용액합성실험에 의한 에트린자이트 결정성장억제 연구)

  • Lee, Hyo-Min;Hwang, Jin-Yeon;Oh, Ji-Ho
    • Journal of the Mineralogical Society of Korea
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    • v.23 no.1
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    • pp.51-61
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    • 2010
  • Ettringite $(Ca_6[Al(OH)_6]_2(SO_4)_3{\cdot}26H_2O)$ is a sulfate mineral that shows a complicate property in concrete. It is often called as "a cancer of concrete" because secondary ettringite formation in hardened concrete often cause expansion and cracking of concrete due to its expansive crystal structure. In the present study, we tested the possibility for crystal growth inhibition of secondary ettringite by crystallization inhibitors that are commercially used for scaling inhibitors in Korea. For the test, we developed a method of ettringite solution synthesis. Three types of crystallization inhibitors were selected and examined the effects On ettringite growth inhibition. The experimental results of ettringite solution synthesis indicated that ettringite was successfully synthesized under condition that the mass balance between calcium hydroxide saturated solution and aluminum sulfate solution was attained. Monosulfate and semisulfate were synthesized when the ratio of $Ca^{2+}$ ions to ${SO_4}^{2+}$ ions was increased. The induction time of ettringite crystallization was less than 2 min. and crystallization was almost completed within an hour. The experimental results of ettringite crystallization inhibition showed that organic PBCT (2-Phosphonobutane-1,2,4-Tricarboxylic Acid) and inorganic SHMP (Sodium Hexametaphosphate) were relatively less effective on ettringite crystallization inhibition under experimental conditions. However, organic HEDP (1-Hydoxyethylidene-1,1-Diphosphonic Acid) effectively prevented ettringite growth with producing amorphous gel phase materials up to inhibitor concentration 0.1 vol.% of aluminum sulfate solution.

Effects of mineralizer and concentration on the morphology of the $CaTiO_3$ powders prepared by hydrothermal method (수열법에 의한 $CaTiO_3$분말 합성 시 광화제와 농도가 입자형상에 미치는 영향)

  • 정항철;서동석;이종국
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.12 no.6
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    • pp.329-334
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    • 2002
  • The $CaTio_3$powder with perovskite structure was synthesized by mixing anatase $TiO_2$and $Ca(OH)_2$powders as starting materials, and KOH or NaOH as mineralizer, followed by hydrothermal method. The change of crystal structure, particle shape and size of the synthesized $CaTiO_3$powder was investigated with kind and concentration of mineralizer. It was found that the spherical particles of 0.7 $\mu$m were obtained when using 1N KOH and the hexahedrons particles of 3$\mu$m were obtained for the case of using 10 N KOH. With increasing KOH concentration, the particle shape was changed from sphere to hexahedrons and its size also increased. When using 1 N NaOH, the powder was consisted of 0.5~1 $\mu$m particle in size, whereas hexahedrons of 1~4 $\mu$m and whiskers more than 10$\mu$m in size was obtained for the 10 N NaOH solution. With increasing NaOH concentration, the particle shape was varied from hexahedrons to whiskers, showing the similar result with the KOH case. It was confirmed from EDS analysis that Na element, which was detected in hexahedrones was not contained in the whiskers.

Photocatalytic and Antipathogenic Effects of TiO2/CuxO (1 (TiO2/CuxO (1)

  • Cho, Sungwoo;Lee, Yong-Im;Kim, Lee-Han;Jung, Dongwoon
    • Journal of the Korean Chemical Society
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    • v.57 no.4
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    • pp.483-488
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    • 2013
  • Copper oxide (CuO) was synthesized from $CuCl_2$ by solution method. Anatase $TiO_2$ particle was dispersed into the solution before preparing CuO, so that $TiO_2$/CuO heterojunction was created through the nucleation of CuO onto the $TiO_2$ surface. Some amount of CuO was reduced to $Cu_2O$ by treating glucose into the solution, thereby preparing $TiO_2/Cu_xO$ complex. The obtained $TiO_2/Cu_xO$ complex showed advanced phtocatalytic activity under the sun light compared with the P-25 sample. In addition, the the $TiO_2/Cu_xO$ complex showed excellent antipathogenic effect.

Aspects of Cellulase Induction by Sophorose in Trichoderma reesei QM9414 (Trichoderma reesei QM9414의 sophorose에 의한 섬유소 분해효소 유도현상에 관하여)

  • 정종문;박희문;홍순우;하영칠
    • Korean Journal of Microbiology
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    • v.23 no.2
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    • pp.77-83
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    • 1985
  • The aim of this investigation was to resolve the contradiction between the results of Sternberg and Mandels (1980, 1982)and those of Nisizawa et al., (1971) in cellulase induction by sophorose, and furthermore to study the conditional effects in sophorose-induced cellulase induction in Trichoderma reesei QM 9414. Sophorose could induce the synthesis of CMCase and ${\beta}-glucosidase$ simultaneously. Optimal induction medium by sophorose had the potassium citrate buffer solution of pH 3.0-4.0 for CMCase, but one of pH 5.0-6.0 for ${\beta}-glucosidase$. At this time, two different types of ${\beta}-glucosidase$ could be induced by sophorose: one was extracellular and had maximum at pH 5.0, the other was intracellular and had maximum activity at pH6.5. Induction study showed that $methyl-{\beta}-glucoside$ was not a true inducer of ${\beta}-glucosidase$ and that large ${\beta}-glucosidase$ induction could be obtained only by the addition of sophorose into the induction medium. Glucose repressed the induction of cellulase by sophorose. The repression of glucose could not be overcome by the addition of cyclic AMP into the induction medium.

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나노입자 페이스트를 이용한 CuInSe2 태양전지 제작

  • Jo, Hyo-Jeong;Seong, Si-Jun;Park, Mi-Seon;Hwang, Dae-Gyu;Gang, Jin-Gyu;Kim, Dae-Hwan
    • Proceedings of the Korean Vacuum Society Conference
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    • 2011.02a
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    • pp.412-412
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    • 2011
  • CI(G)S계 태양전지는 화합물 반도체로서, 우수한 광 전류 변환 효율을 보이며, 광조사 등에 의한 열화가 없어 유망한 태양전지로 인정받고 있다. CI(G)S계 태양전지를 구성하는 흡수층을 제조하는 방법은 진공 기반의 공증착법 및 스퍼터-셀렌화법이 대표적이며, 액상의 전구체 물질을 도포하고 이를 고온 열처리하는 용액공정법도 최근 많은 연구가 이루어지고 있다. 진공 증착법은 고효율의 흡수층을 제조할 수 있고 상용화에 적합한 방법이다. 그러나 고가의 진공 장비를 이용하는 진공증착법은 원가 절감 관점에서 한계를 지니고 있어, 미래의 저가 공정 실현을 위해 용액 기반 흡수층 제조법도 다양한 접근법으로 연구되고 있으며 현재까지는 진공공정에 비해 상대적으로 낮은 변환효율이 큰 문제점으로 인식되고 있다. 용액 공정에서 전구체 물질의 코팅법으로는 spray법, spin coating법, drop-casting법, doctor-blade법 등이 있으며, 이들 중 양산 공정에 실용화되기 가장 적합한 것으로 보이는 방법으로는, 화합물 나노입자 페이스트를 기재 상에 doctor blade 법으로 코팅한 후에 이를 열처리하여 흡수층을 제조하는 방법을 들 수 있다. 이러한 방법은 균일한 흡수층을 저비용으로 제조할 수 있는 장점은 있지만, 전구체로 사용하는 화합물 나노입자들이 화학적 및 열적으로 매우 안정한 물질이므로, 최종 흡수층에서 큰 결정을 얻기 어렵고, 그 결과 효율이 낮아지는 단점이 있다. 따라서, 치밀하고 조대한 grain 형성을 위하여 CISe 균일한 나노입자를 합성하고 셀레늄을 포함하는 용액을 추가로 도포하여 열처리 공정에서 Se의 손실을 막아 입자를 성장시키는 방법과 In-Se 균일한 나노입자를 합성한 후 Cu, Se이 포함된 용액을 도포하여 코어-쉘 (InSe/CuSe)을 제작하고 이를 Se 분위기하 열처리 하여 흡수층의 결정성을 증진시키고자 하였다. 또한 다양한 방법으로 제작한 CuInSe2 나노입자로 잉크를 제작하여 닥터블레이드 공정을 적용하여 박막을 제작하고 소자 적용성을 평가하였다.

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Synthesis of Heteroatom-Carbon Nanosheets by Solution Plasma Process (솔루션 플라즈마를 이용한 이종 원소 카본 나노시트의 합성)

  • Hyeon, Gwang-Ryong;Jeong, Gwang-Hu;Park, Il-Cho;Lee, Jeong-Hyeong;Han, Min-Su;Kim, Seong-Jong;Saito, Nagahiro
    • Proceedings of the Korean Institute of Surface Engineering Conference
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    • 2018.06a
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    • pp.114-114
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    • 2018
  • 탄소 재료는 뛰어난 물성에서 다양한 재료로의 응용이 기대되고 있다. 특히, 이종 원소 함유 카본 재료는 전기적 특성과 촉매성의 발현 등 새로운 기능을 카본 재료에 부여할 수 있어서 연료 전지, 에너지 저장, 태양 전지 등에의 응용이 기대되고 있다. 최근, 용액 중의 저온 플라즈마인 솔루션 플라즈마(solution plasma process)를 이용하여 벤젠 용액 등에서 탄소 재료 합성에 성공하였다. 그러나 기존의 연구에서는 솔루션 플라즈마 프로세스를 이용하여 합성한 이종원소 카본은 전도성이 낮아 이종원소의 함유량을 낮추는 고온의 열처리가 필요했다. 따라서 본 연구에서는 우수한 물리적 전기적 특성을 갖는 그래핀(graphene)과 같은 이종 원소 카본 나노시트(heteroatom carbon nanosheets)의 합성 및 메커니즘(mechanism)에 대해 검토하였다. 다양한 이종원소를 포함한 유기용매 안에 바이폴라 펄스 전원에 의한 전압을 두 텅스텐 전극 간에 인가하고, 솔루션 플라즈마를 생성하여 이종원소 카본 재료를 합성했다. 플라즈마 생성은 텅스텐 봉을 전극으로 사용하고 전압을 2.0 kV, 펄스 주파수를 200 kHz, 펄스 폭을 $1.0{\mu}s$, 전극 간 거리를 1.5 mm에서 일정하게 유지하며 200 mL 유기용매 중에서 방전시키는 것으로 재료를 합성했다. 플라즈마 방전 후, 필터을 이용하여 흡인 여과한 뒤 $200^{\circ}C$에서 1 시간 동안 건조 시켰다. 건조 후의 이종원소 카본의 물리적 특성을 원소 분석, X선 회절 법(XRD), 저항률 측정, 투과형 전자 현미경(TEM) 및 라만 분광법, 전자 현미경(SEM), X-선광전자분광기(XPS)등을 이용하여 카본의 형상 및 특성을 분석하였다. 그 결과 다양한 이종원소를 포함한 유기용매 중 2-pyrrolidone을 사용했을 때, 이종 원소 카본 나노시트를 합성하는데 성공하였다. 또한, 이 연구방법을 통해서 솔루션 플라즈마 프로세스를 통한 카본 나노시트 합성의 메커니즘을 규명하였다.

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Synthesis of ZnS : Cu nano-crystals and structural and optical properties (ZnS : Cu nano 업자의 합성 및 구조적.광학적 특성)

  • 이종원;이상욱;조성룡;김선태;박인용;최용대
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.12 no.3
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    • pp.138-143
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    • 2002
  • In this study, ZnS: Cu nano-crystals are synthesized by solution synthesis technique (SST). The structural properties such as crystal structure and particle morphology, and the optical properties such as light absorption/transmittance, energy bandgap, and photoluminescence (PL) excitation/emission are investigated. In an attempt to realize the Cu-doping easiness, the synthesis temperature (~$80^{\circ}C$) is applied to the synthesis bath, and the thiourea is used as sulfur precursor, unlike other general chemical synthesis route. Both undoped ZnS and ZnS : Cu nano-crystals have the cubic crystal structure and have the spherical particle shape. The position of light absorption edge is ~305 nm, indicating the occurrence of quantum size effect. The PL emission intensity and line-width are maximum and minimum, respectively, for Cu-doping concentration 0.03M. In particular, the dependence of PL intensity and line-width on the Cu-doping concentration for ZnS : Cu nano-crystals synthesized by SST is reported for the first time in this study. Experimental results of the absorption edge and the PL excitation show that the main emission peak of ZnS : Cu nano-crystals (~510 nm) in this study is due to the radiative recombination center in the energy bandgap induced by Cu dopant.

Synthesis and characterization of $BaTiO_3$ fine particles by hydrothermal process (수열합성법에 의한 미립의 $BaTiO_3$ 분말합성 및 특성)

  • 배동식;주기태;한경섭;최상흘
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.8 no.4
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    • pp.563-566
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    • 1998
  • $BaTiO_3$ fine particles were prepared by hydrothermal process from titanium tetra-isoproproxide ($Ti(OiPr)_4$) and barium hexa-hydroxide ($Ba(OH)_2{cdot}8H_2O$) as raw materials. The fine particles were obtained at the temperature range of 160 to $185^{\circ}C$. The properties of $BaTiO_3$ particles were studied as a function of various parameters such as reaction temperature, reaction time and Ba/Ti ratio, etc. The average particle size of $BaTiO_3$ increased with increasing reaction temperature and time. After hydrothermal treatment at $170^{\circ}C$ for 8 h, the average particle size of $BaTiO_3$ was about 30 nm and the particle size distribution was narrow.

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