전자 소재 물성을 설계하기 위한 원자 단위로 얇은 결정 박막의 적층

김철주,Kim, Cheol-Ju 한국전기전자재료학회 2019 전기전자재료 Vol.32 No.5

Some Crystalline Properties and Growth Condition of BP(100)Epitaxially Grown on Si(100) Substrates

김철주,고연규,안철,Kim, Chul Ju,Koh, Youn Kyu,Ahn, Chul The Institute of Electronics and Information Engin 1986 전자공학회논문지 Vol.23 No.6

Boron monophosphide(100) was eitaxially grown on Si(100) substrate by thermal reaction of B2H6 and PH3 in hydrogen ambient. In an LPCVD system, the growth condition was studied as a function of gas mixture composition and temperature. For the growth temperature of 950\ulcorner in the constant flow rate (partial pressure) of B2H6, n-BP with c(2x2) surface structure was obtained in the PH3 partial pressure of 300-500 cc/min. On the other hand, for the growth temperature of 1080\ulcorner, p-BP with surface structure was observed for the PH3 partial pressure of 400-500cc/min.

규산(硅酸)나트륨 수용액(水溶液)의 솔-젤 반응속도론적(反應速度論的) 고찰(考察)

김철주,윤호성,장희동,Kim, Chul-Joo,Yoon, Ho-Sung,Jang, Hee-Dong 한국자원리싸이클링학회 2008 資源 리싸이클링 Vol.17 No.6

본 연구에서는 yellow silicomolybdate method를 이용하여 규산나트륨 수용액의 특성, 핵 생성에 필요한 규산나트륨 수용액의 산화반응 특성 그리고 출발용액의 솔젤 반응특성을 기초로 하여 실리카 솔 형성에 대한 반응속도론적 고찰을 하였다. $SiO_2$를 2wt% 함유한 규산나트륨 수용액은 황산으로 산화시키기에 적당하였으며, 규산나트륨 수용액중의 나트륨 이온을 제거한 후, 안정된 실리 케이트 수용액을 얻기 위한 용액의 pH는 9 이상이었다. 규산종과 실리카 핵 표면 사이의 축중합 반응에 관한 속도론적 연구는 반응온도 $20{\sim}80^{\circ}C$, 수용액의 pH 10에서 수행하였다. 반응은 두 영역으로 구분되는데, 규산종의 농도가 높은 영역에서는 축중합 반응에 의해 제한을 받으며, 낮은 농도 영역에서는 화학흡착된 규산종이 실리카로 응축되는 공정에 영향을 미친다. 전체 축중합 반응은 규산종 농도의 1차 반응으로 진행되며, 축중합 반응은 무정형 실리카의 용해도에 접근하기 보다는 가평형점($C_x$) 향하여 진행된다. 본 연구조건에서 무정형 실리카의 용해열은 3.34 kcal/mol이었고 축중합 반응의 활성화에너지는 3.16 kcal/mol이었다. The properties of sodium silicate solution were surveyed by using the yellow silicomolybdic method, and the formation of silica sol from sodium silicate solution and the growth of silica sol were investigated in this study. The $SiO_2$ content of 2 wt% in sodium silicate solution was proper to oxidize sodium silicate with sulfuric acid. After the removal of sodium ions in sodium silicate solution, the pH of silicate solution had to be controlled above 9 for the stabilization of silicate solution. The condensation between silicic acid species and silica nuclei surfaces has been studied at $20{\sim}80^{\circ}C$ and pH 10 in silicate solutions with silica nuclei. The reaction falls into two kinetics regimes, limited at high silicic acid species concentration by polymerization, but at lower concentration by a process whereby deposited silicic acid species condenses further to silica. The overall condensation is first-order in silicic acid species concentration, proceeded toward to pseudo equilibrium concentration, $C_x$, rather than the solubility of amorphous silica. The heat of solution of amorphous silica was 3.34 kcal/mol and exhibits an Arrhenius temperature dependence with an apparent activation energy of 3.16 kcal/mol in the range of $20{\sim}80^{\circ}C$.

소디움실리케이트 수용액(水溶液)으로부터 솔-젤 반응(反應)에 의해 제조(製造)된 실리카 솔 입자특성(粒子特性) 고찰(考察)

김철주,김성돈,장희동,윤호성,Kim, Chul-Joo,Kim, Sung-Don,Jang, Hee-Dong,Yoon, Ho-Sung 한국자원리싸이클링학회 2009 資源 리싸이클링 Vol.18 No.6

소디움실리케이트 수용액으로부터 나트륨이온이 제거된 핵생성 산화실리케이트 수용액과 실리케이트 수용액을 pH 10~11로 조절하여 혼합한 다음, $20{\sim}80^{\circ}C$에서 솔-젤 반응하여 실리카 솔 입자를 제조하였다. 이 때 yellow silicomolybdate method를 이용하여 소디움실리케이트와 나트륨이온이 제거된 실리케이트 수용액의 특성과 이들 출발용액으로부터 솔-젤 반응에 의해 제조된 실리카 솔의 입자특성에 대하여 고찰하였다. $SiO_2$를 2 wt% 함유한 소디움실리케이트 수용액은 약 95% 이상의 반응성 실리케이트를 함유하며, 솔-젤 반응에 참여하는 반응성 실리케이트는 전체 실리카 기준 약 50% 정도이다. 반응온도가 증가함에 따라 silanol(Si-OH) 결합구조의 흡수피크 세기는 감소하고, siloxane(Si-O-Si) 결합구조의 흡수피크 세기가 증가하였다. 반응조건별로 제조된 실리카 솔 수용액의 zeta potential은 -40~-60 mV 범위로 분산성이 좋은 상태를 유지하였다. 실리카 솔 입자크기는 5~10 nm로 반응온도 증가에 따라 크기가 약간 감소하였다. 실리카 솔 제조 후, 2차 입자 성장을 위하여 실리케이트 수용액을 재 첨가하였을 경우에 실리카 솔입자 크기가 약 20 nm로 증가하였다. Silica sol was prepared from the mixture of sodium silicate solution and oxidized silicate solution in which sodium had been removed by sol-gel process. The properties of sodium silicate solution and silicate solution thus prepared were characterized by yellow silicomolydate method. Moreover, the formation and growth of silica sol from sodium silicate solution was investigated. Sodium silicate solution with 2% of $SiO_2$ contains 95% of reactive silicate, and 50% of reactive silicate participates sol-gel reaction. From the results of FT-IR analysis, it was found that the intensity of silanol bond decreased and the intensity of siloxane bond increased with increasing reaction temperature. Zeta potential of silica sol prepared at each condition was -40~-60 mV and it could be known that silica sol in this study was well dispersed. The silica sol with 5~10 nm size could be prepared by heating the mixed solution of sodium silicate and silicate solution. And the silica sol grew into about 20 nm as silicate solution was added to silica sol solution.

염화네오디뮴 수용액으로부터 탄산네오디뮴 결정화

김철주,윤호성,김준수,이승원,Kim, Chul-Joo,Yoon, Ho-Sung,Kim, Joon-Soo,Lee, Seung-Won 한국자원리싸이클링학회 2007 資源 리싸이클링 Vol.16 No.2

본 연구는 염화네오디뮴 수용액으로부터 탄산수소암모늄의 첨가에 의한 탄산네오디뮴 합성 시, 반응에 따라 형성되는 탄산네오디뮴 결정에 대하여 고찰하였다. 결정형의 탄산네오디뮴을 얻기 위해서는 염화네오디뮴 수용액에 투입되는 탄산수소암모늄 수용액의 농도와 반응온도가 중요한 역할을 한다. 무정형의 탄산네오디뮴은 핵생성을 통한 일차입자들의 응집에 의하여 형성되며, 반응물의 농도 및 반응온도 등을 증가시켜 반응속도를 빠르게 함으로서 결정형의 탄산네오디뮴을 얻을 수 있었다. 또한 반응조건에 따라 lanthanite[$Nd_2(CO_3)_3{\cdot}8H_2O$]와 tengerite[$Nd_2(CO_3)_3{\cdot}2.5H_2O$] 결정구조를 갖는 탄산네오디뮴을 합성할 수 없었으며, lanthanite 구조의 탄산네오디뮴은 온도에 민감하고 불규칙한 모양의 덩어리 형태를 가지며, 반면에 tengerite 구조의 탄산네오디뮴은 침상의 형태를 가지고 있음을 알 수 있다. 열분해 거동 고찰 결과 250까지 탄산네오디뮴의 결정수가 분해되고 $420^{\circ}C$부근에서 $CO_2$가 분해되어 $Nd_2O_2CO_3$가 형성되며, $620^{\circ}C$에서 산화네오디뮴 결정화가 시작하여 $700^{\circ}C$ 부근에서 최종적으로 산화네오디뮴의 형성되는 것을 알 수 있다. 또한 소성된 산화네오디뮴의 형상은 탄산네오디뮴의 형상에 의하여 영향 받고 있음을 알 수 있다. In this study, the crystallization of neodymium carbonate from neodymium chloride solution by addition of ammonium bicarbonate was investigated. The concentration of reactants such as neodymium chloride and ammonium bicarbonate, and reaction temperature play an important part in order to obtain the crystal of neodymium carbonate. It seemed that amorphous neodymium carbonate was prepared by aggregation of primary particles formed through nucleation. If reaction rate was increased by increasing the concentration of reactants and reaction temperature, then neodymium carbonate crystal could be obtained. Lanthanite-type neodymium carbonate[$Nd_2(CO_3)_3{\cdot}8H_2O$] and tengerite-type neodymium carbonate[$Nd_2(CO_3)_3{\cdot}2.5H_2O$] could be obtained with reaction renditions. Lanthanite-type neodymium carbonate was sensitive to temperature. The thermal decomposition of neodymium carbonate contained the processes or dehydration, decarbonation and crystalization of $Nd_2O_3$. The shape of lanthanite-type neodymium carbonate was irregular lump type, and tengerite-type neodymium carbonate had the shape of needle type. The shape of $Nd_2O_3$ was affected by the shape of neodymium carbonate.

열파이프의 제조 및 성능시험

김철주,이준엽,Kim, Chul-Ju,Lee, Joon-Yeob 대한설비공학회 1989 설비저널 Vol.18 No.1

금속의 평면 접촉면에서 표면부식에 의한 열접촉 저항의 변화

김철주,김원근,Kim, C.J.,Kim, W.G. 대한설비공학회 1991 설비공학 논문집 Vol.3 No.4

The corrosion effects on thermal contact resistance were experimentally studied for a given contact interface of a couple of metals. 2 cylindrically shaped test pieces, the one was carbon steel whose surface was machined by lathe and the other was stainless steel, ground, were come into contact under pressure, and then submerged to $HNO_3$ gas environment. While the corrosion process was going on, the thermal contact resistance was measured with time. The experiment was performed for 2 cases; 1) Highly compress the test pieces and then bring them to $HNO_3$ gas environment. 2) Anteriorly corrode the interface under low contact pressure and then increase the contact pressure. The results were as follows; In 1st. case of experiment, the thermal contact resistance seemed to be very stable, and showed low values with a tendancy of small decrease with time. But in 2nd. case the resistance was unstable and jumped to a value of 200-250% more then that expected for uncontaminated interface. More over it demonstrated some increase with time.

경제발전과 도서관

김철주,Kim, Cheol-Ju 한국도서관협회 1976 圖協月報 Vol.17 No.8

Preparation of Nano-sized Pt Powders by Solution-phase Reduction

김철주,윤호성,조성욱,손정수,Kim, Chul-Joo,Yoon, Ho-Sung,Cho, Sung-Wook,Sohn, Jung-Soo The Korean Institute of Resources Recycling 2007 資源 리싸이클링 Vol.16 No.5

백금은 물리화학적 특성에 기인하여 많은 분야에서 중요한 역할을 하고 있으며, 이러한 분야에서는 아주 미세한 백금의 사용을 요구하고 있다. 그러므로 본 연구에서는 액상에서 환원제를 사용하여 백금염을 환원시킴으로서 나노크기의 백금을 제조하는 방법에 대하여 알아보았다. 수용액상에서 C14TABr과 $H_2[PtCl_6]$ 상호작용은 $[C1_4TA]_2[PtCl_6]$의 유기백금염 화합물을 형성한다. 단분산 나노 백금입자를 얻기 위해서는 $C1_4TABr$과 $H_2[PtCl_6]$ 농도가 각각 cmc와 0.32 mM 이상이 되어야 한다. $H_2[PtCl_6]$와 C14TABr 농도가 증가함에 따라 백금입자 크기가 증가하였으며, 백금입자의 형태는 C14RABr농도 증가에 따라 제어가 가능하였다. Platinum plays an important role in many applications because of its extraordinary physical and chemical properties. All these applications require the use of platinum in the finely divided state. Therefore the preparation of platinum nanoparticles by reducing platinum-surfactant salt with reducing agent in the solution was investigated in this study. The net interaction between C14TABr and $H_2[PtCl_6]$ in aqueous solution results in the formation of $[C14TA]_2[PtCl_6]$. The concentration of C14TABr and the concentration of $H_2[PtCl_6]$ has to be above cmc and 0.32 mM, respectively in order to obtain complex-micelle aggregation for mono dispersed Pt particles. Pt particle size increases with increasing $H_2[PtCl_6]$ and C14TABr concentration. And the shape of Pt particles was well controlled with increasing surfactant concentration.

밀폐형 2상 열사이폰의 Pool 내부 Pulse Boiling에 관한 연구

김철주,문석환,강환국,Kim, Cheol-Ju,Mun, Seok-Hwan,Gang, Hwan-Guk 대한기계학회 1997 大韓機械學會論文集B Vol.21 No.10

Pulse boiling, the unsteady periodic boiling phenomenon appearing in the evaporator of thermosyphons was investigated by many researchers. In the present study investigations were conducted to examine the evolution of flow patterns at the evaporator, and changes in thermodynamic state that each of liquid pool and vapor experiences through 1 cycle of pulse boiling process. For wall and liquid pool the degree of superheat for the onset of nucleation was examined. It revealed that the degree of superheat increased with the increase of pulse period, reaching to 16.5 deg.C and 23 deg.C for liquid pool and evaporator wall respectively at .tau.=80 sec. The data on flow patterns obtained through series of operation tests were plotted in the coordinates of heat flux and vapor pressure to get a regime map. Further this map could be used to figure out the conditions of pulse boiling for a thermosyphon.