• Korean Chemical Engineering Research
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• 제52권4호
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• pp.436-442
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• 2014

염화코발트 용액을 사용하여 전자기파와 진동에 영향을 받지 않는 원거리 실시간 광섬유 온도 감지 센서를 개발하였다. 염화코발트 용액을 제조하기 위하여, 물과 에탄올은 부피 비율로 10%와 90%로 고정하고, 용해되는 염화코발트의 양을 다양하게 변화시켰다. 제조된 염화코발트 용액은 자외-가시선 분광 광도계를 사용하여, 온도 변화에 따른 655 nm 파장의 투과도를 측정하였다. 또한 제조된 30.8 mM 염화코발트 수화물 용액에 polyvinyl butyral을 용해시켜 겔화한 후, 온도 변화에 따른 655 nm 파장의 투과도 측정 및 센서 적용 후 광 파워 분석을 실시하였다. 투과도와 광 파워 측정 결과, $25^{\circ}C$에서 66.8%와 149.5 nW, $70^{\circ}C$에서는 7.1%와 48 nW로 각각 나타나, 온도가 증가함에 따라 투과도와 광 파워 모두 감소하는 경향을 보였다. 본 실험에서 제조된 겔화 염화코발트/polyvinyl butyral은 온도 변화에 따라 655 nm 파장에 대한 광 투과도와 광 파워가 변하는 점을 이용하여 온도 변화를 감지하기 위한 광섬유 센서로 사용 가능함을 확인하였다.

• 문화기술의 융합
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• 제9권3호
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• pp.587-592
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• 2023

CoCl₂·6H₂O 수용액을 결정성셀룰로오스에 함침시켜 건조한 후, 하소, 소성을 통하여 산화코발트(Co₃O₄·CoO) 초미세입자를 합성하였다. 합성된 코발트 산화물 입자의 결정구조 및 표면구조를 주사전자현미경(SEM)과 X-선회절분석(XRD)으로 조사하였다. CoCl₂·6H₂O 수용액을 함침시키는 매개체로 사용한 결정성셀룰로오스(crystalline cellulose)는 470℃ 정도에서 열분해 되었고, Co₃O₄ 결정상은 350℃에서 생성되기 시작하였다. Co₃O₄ 결정상은 500℃까지 유지되었으며, 500℃ 이상의 온도에서는 CoO 결정상으로 변화하는 것을 알 수 있었다. 열처리 온도가 증가함에 따라 산화코발트 입자의 크기가 커지는 현상이 나타났으며, 900℃ 이상의 온도에서는 입자간 용융이 일어나는 것이 관찰되었다. 하소온도 700℃ 이하의 온도에서 입자크기 2-10㎛의 Co₃O₄와 CoO의 초미세입자가 생성되는 것을 확인하였다.

• 대한화학회지
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• 제31권3호
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• pp.231-235
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• 1987

니켈중 미량의 코발트를 분리하는데 액상음이온교환수지인 Amberlite LA-2를 이용하였다. 10M 염소이온 (4M HCl + 6M LiCl) 용액중에서 코발트는 ${CoCl_3}^-$를 형성하여 Amberlite LA-2 1ml에 2.175meq 추출되었다. 그러나 같은 조건의 염소이온용액에서 니켈은 착음이온을 형성하지 않으므로 전연 추출되지 않았다. 수지층에 추출된 코발트는 0.4M 질산용액에 의해 정량적으로 용리되었다. 코발트 50mg과 니켈 500mg을 녹인 합성시료용액중에 본 분리 방법을 적용시킨 결과 99.6%의 코발트를 분리회수 하였다.

• 한국재료학회지
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• 제26권11호
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• pp.662-669
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• 2016

In order to identify changes in the nature of the particles due to changes in the inflow rate of the raw material solution, the present study was intended to prepare nano-sized cobalt oxide ($Co_3O_4$) powder with an average particle size of 50 nm or less by spray pyrolysis reaction using raw cobalt chloride solution. As the inflow rate of the raw material solution increased, droplets formed by the pyrolysis reaction showed more divided form and the particle size distribution was more uneven. As the inflow rate of the solution increased from 2 to 10 ml/min, the average particle size of the formed particles increased from about 25 nm to 40 nm, while the average particle size did not show significant changes when the inflow rate increased from 10 to 50 ml/min. XRD analysis showed that the intensity of the XRD peaks increased remarkably when the inflow rate of the solution increased from 2 to 10 ml/min. On the other hand, the peak intensity stayed almost constant when the inflow rate increased from 10 to 50 ml/min. With the increase in the inflow rate from 2 to 10 ml/min, the specific surface area of the particles decreased by approximately 20 %. On the contrary, the specific surface area stayed constant when the inflow rate increased from 10 to 50 ml/min.

• 한국재료학회지
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• 제24권1호
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• pp.25-32
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• 2014

In this study, nano-sized cobalt oxide powder with an average particle size below 50 nm was prepared from a cobalt chloride solution by the spray pyrolysis process. The influences of reaction temperature on the properties of the generated powder were examined. The average particle size of the particles formed based on the spray pyrolysis process at a reaction temperature of $700^{\circ}C$ is roughly 20 nm. Moreover, most of these particles cannot appear with an independent type, thereby coexisting in a droplet type. When the reaction temperature increases to $800^{\circ}C$, the average particle size not only increases to roughly 40 nm but also shows a more dense structure while the ratio of particles which shows a polygonal form significantly increases. As the reaction temperature increases to $900^{\circ}C$, the distribution of the particles is from roughly 70 nm to 100 nm, while most of the particle surface is more intricately close and forms a polygonal shape. When the reaction temperature increases to $1000^{\circ}C$, the particle size distribution of the powder shows an existing form from 80 nm to at least 150 nm in an uneven form. As the reaction temperature increases, the XRD peak intensity gradually increases, yet the specific surface area gradually decreases.

• 한국분말재료학회지
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• 제10권4호
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• pp.228-234
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• 2003

In the present study, the focus is on the synthesis of titanium carbide/cobalt composite powder by the spray thermal conversion process using metallic salt solution as the raw materials. Two types of oxide powders of Ti-Co-O system were prepared by the spray drying of two types of metallic salt solutions : titanium chloride-cobalt nitrate and $TiO_2$ powder-cobalt nitrate solutions. These oxide powders were mixed with carbon black, and then these mixtures were carbothermal reduced under a flowing argon atmosphere. The changes in the phase structure and thermal gravity of the mixtures during carbothermal reduction were analysed using XRD and TG-DTA. In the case of using the titanium chloride-cobalt nitrate solution, it could not be obtained TiC/Co composite powder due to contamination of the impurities during the spray drying of the solution. However, in tile case of using the $TiO_2$ powder-cobalt nitrate scullion, TiC-15 wt. %Co composite powder could be synthesized by the spray thermal conversion process. The synthesized TiC-15 wt. %Co composite powder at 120$0^{\circ}C$ for 2 hours has average particle size of 150 nm.

• 대한화학회지
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• 제19권1호
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• pp.53-64
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• 1975

Co$Cl_2$-THF-MMA계에 대한 중합반응을 조사한 결과 다음과 같은 사실을 알았다. 즉 중합시간에 따른 중합변화율이 6${\sim}$7% 미만의 초기에는 직선적인 관계가 있으나 차차 중합속도가 감소했다가 그 후에는 라디칼중합의 경우와 같이 자동가속화현상을 볼 수 있었다. 개시물인 염화 코발트(II)의 농도가 증가하면 중합속도가 증가했다가 약 $3.4{\times}10^{-4}$mole/l 이상이 되면 반대로 중합속도는 감소하였다. 그리고 단위체인 MMA의 농도에 따라 중합속도는 1.38의 반응차수를 가지고 증가하였다. 라디칼중합에 대한 억제물인 DPPH를 첨가하면 억제기간이 생기고 이 억제기간은 DPPH의 농도에 따라 증가하였다. 이 중합계에 대한 겉보기 총 활성화 에너지는 13.2kcal/moe임을 알았다. MMA($M_1$)과 styrene($M_2$)의 공중합체에 대한 단위체 반응성비는 $r_1$=2.35, $r_2$=0.78이었다. 그리고 이러한 실험결과에서 이 계에 의한 중합개시 메카니즘을 논의하여 디라디칼에 의한 중합이 우세하게 일어난다고 생각되었다.

• 한국산업보건학회지
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• 제4권1호
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• pp.43-70
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• 1994

The effects of potassium chromate (500ppm/500ppm), potassium dichromate (500ppm/500ppm), cobalt chloride (100ppm/10ppm), methylmercuric chloride (100ppm/10ppm) on the biosynthesis of phospholipid and their composition of fatty acids in E.coli and B.subtilis were analyzed. The contents of phosphatidylethanolamine, phosphatidylcholine, phosphatidylinositol, phosphatidylglycerol, cardiolipin and total lipids in treatment with metal compounds were lower to compare with the control. The major fatty acid utilized for biosynthesis of phospholipid was palmitic acid in control of E.coli and B.subtilis. However, in treatment with metal compounds, changes of fatty acid composition utilized for phospholipid formation were as follows. In E.coli major fatty acids were palimitic acid (ave. 26.26%) and cis-vaccenic acid (ave. 10.94%) in treatment with potassium chromate, palmitic acid (ave. 31.41%/31.42%) and stearic acid (ave. 17.92%/19.41%) in treatment with potassium dichromate and cobalt chloride. And in treatment with raethylmercuric chloride, palmitic acid (ave. 26.66%), stearic acid (ave. 15.50%) and cis-vaccenic acid (ave. 20.59%) were used in phospholipid formation. In B.subtilis, the major fatty acid was palmitoleic acid (ave. 15.29% /10.22%) in treatment with potassium chromate and cobalt chloride, and stearic acid (ave. 16.01%) in treatment with potassium dichromate. On the other hand, cis-vaccenic acid (ave. 9.09%), palmitic acid (ave. 17.23%), stearic acid (ave. 6.66%), myristic acid (ave. 6.34%) and lauric acid (ave. 4.75%) were analyzed into major fatty acids in treatment with methylmercuric chloride. As shown in results, specific fatty acid pattern was came out in treatment with metal compounds according to bacteria and treatments.

• Bulletin of the Korean Chemical Society
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• 제18권4호
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• pp.406-409
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• 1997

The various cobalt(Ⅱ) complexes were synthesized and characterized using tris-(2-benzimidazolylmethyl)amine (ntb) as a ligand where the ntb plays as a tripodal tetradentate ligand to form complexes with a trigonal pyramidal geometry. The complexes have 5 and 6 coordinate cobalt(Ⅱ) ions depending on the additional ligand used. In each complex the additional ligand, chloride anion, or acetate anion occupies the "open" site trans to the apical tertiary nitrogen atom of ntb ligand. Complex 1, [Co(Ⅱ)(ntb)Cl]Cl has a trigonal bipyramidal geometry. This geometry was easily constructed using ntb as a tetradentate ligand and chloride as a monodentate ligand. The complex is isostructural to the corresponding manganese(Ⅱ) complex. Crystal data are as follows: [Co(Ⅱ)(ntb)Cl]Cl·MeOH, 1. triclinic space group P1; a=13.524(2) Å, b=14.037(2) Å, c=17.275(1) Å; α=78.798(9), β=84.159(8)°, γ=65.504(9)°; V=2929.6(6) Å3; Z=4; R1=0.0715, wR2=0.1461 for reflections of I > 2σ(I). Six coordinate complex 2 [Co(ntb)(OAc)](OAc) was synthesized using ntb as a tetradentate ligand and acetate as a bidentate chelating ligand.

• 폴리머
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• 제29권4호
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• pp.338-343
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• 2005

Chloride계 전이금속 촉매의 존재 하에서 ABS/PC/triphenyl phosphate 컴파운드의 열분해 거동을 TGA(thermogravimetric analysis)를 통해서 조사하였다. Chloiide계 전이금속 촉매(cobalt chloiide, ferric chloride, nickel chloride 및 zinc chloride)는 ABS/PC/triphenyl phosphate 컴파운드의 열분해 과정에서 화학반응을 야기하여, 질소분위기에서 숯(char) 형성이 관찰되었으며, $600^{circ}C$에서 $3\~l3\%$의 비휘발성 눈을 형성하였다. 이와 같은 질소분위기에서의 ABS/PC/triphenyl phosphate 컴파운드의 숯 생성은 chloride계 전이금속 촉매의 가교효과(crosslinking effect)로 추정된다. 한편, 공기분위기에서는 생성된 숯은 고온 산화반응에 의해서 역분해되었다.