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

• 자원환경지질
• /
• 제53권1호
• /
• pp.1-9
• /
• 2020

이산화탄소 고정화 및 탄산화 반응에는 칼슘(Ca)과 마그네슘(Mg)과 같은 알칼리토류 금속을 함유하고 있는 사문석(serpentine, Mg₃Si₂O₅(OH)₄) 규회석(wollastonite, CaSiO₃), 감람석(olivine, Mg₂SiO₄)과 같은 칼슘/마그네슘 실리케이트 광물(Ca/Mg-silicate mineral)들이 주로 이용되어 왔다. 특히 사문석은 탄산화가 가능한 자연물질 중 자연계 내에 풍부한 매장량을 갖고 있으며, 우수한 반응성 때문에 광물탄산화에 가장 적절한 출발물질로 인식되어 있다. 따라서 본 연구는 사문석을 출발물질로 사용하여 산성 용액 내에서 이산화탄소의 압력이 탄산화 효율에 미치는 영향력을 확인하고자 하였다. 탄산화 실험 조건은 황산용액 0.3~1 M, 반응온도 100℃ 및 150℃ 그리고 이산화탄소의 부분압력 0~3 MPa이며, 탄산화법은 수정된 직접탄산화법(modified direct method)으로 실시하였다. 또한 탄산화 효율을 높이고자 liquid pump로 NaOH 용액을 주입하여 pH를 13으로 조절하였다. 탄산화율은 황산의 농도 및 반응온도에 비례하여 증가하였으며, 3 MPa의 이화탄소를 주입한 조건에서의 탄산화율이 이산화탄소를 첨가하지 않은 조건의 탄산화율보다 높았다. 반응결과 황산용액 1 M과 이산화탄소 부분압 3 MPa, 반응온도 150℃에서 용출 및 탄산화 실험 후 약 85%의 상당히 높은 탄산화율이 분석되었다. 따라서 산성용액에서 이산화탄소의 압력이 사문석 내의 Mg 용출에 영향을 미치는 것으로 확인되었다. Mg의 용해속도는 Si의 용해속도보다 높아 반응 후 사문석의 Mg : Si의 비가 약 1.5에서 0.1미만으로 급속하게 감소하여, 사문석의 구조 내에 불완전한 Si 사면체 층 골격구조(Mg-depleted skeletal phase)가 분석되었다.

• 열처리공학회지
• /
• 제27권1호
• /
• pp.15-22
• /
• 2014

This study is to investigate the phase changes and cold workability after isothermal transformation at $780^{\circ}C$ by using the high temperature gas nitrided (HTGN) STS 430 ferritic stainless steel specimens. The phase diagram of STS 430 steel obtained by calculation showed that the phase appeared at $1100^{\circ}C$ showed as ${\alpha}+{\gamma}{\rightarrow}{\gamma}{\rightarrow}{\gamma}+Cr_2N{\rightarrow}{\gamma}+Cr_2N+CrN$ with increasing nitrogen concentration. Also, the transformation of ${\gamma}{\rightarrow}Cr_2N$ during heat treatment isothermally at $780^{\circ}C$, nitrogen pearlite with lamellar type was fully formed at the nitrogen permated surface layer for 10 hrs. However, this transformation was not completed for 1 hr, resulting nitrogen pearlite plus martensite. The cold rolled specimen of isothermally transformed at $780^{\circ}C$ for 10 hrs after high temperature gas nitriding decreased the layer thickness of nitrogen pearlite inducing the deformation of hard $Cr_2N$ phase. the dissolution rate of $Cr_2N$ phase increased rapidly with increasing cold rolling ratio. Specimens with the microstructure of nitrogen pearlite (isothermally transformed at $780^{\circ}C$ for 10 hrs) were possible to cold rolling without crack formation. However, the mixed structures of nitrogen pearlite + martensite (isothermally transformed at $780^{\circ}C$ for 1 hr) were impossible to cold deformation without cracking.

• 한국지하수토양환경학회:학술대회논문집
• /
• 한국지하수토양환경학회 2006년도 총회 및 춘계학술발표회
• /
• pp.303-306
• /
• 2006

Using a variety of chemical geothermometers we estimate the temperature of a deep geothermal reservoir in relation to thermal groundwater in the Bugok area, southern Korea, in order to assess the potential use of geothermal energy in South Korea. Thermal water at Bugok has been exploited down to about 400 m below the land surface and shows the highest outflow temperatures (up to $78{\circ}C$) in South Korea. Based on the hydrochemical data and occurrence, groundwater in Bugok can be classified into three groups: $Na-SO_4$ type thermal groundwater (CTGW) occurring in the central part (about 0.24 $km^2$) $Ca-HCO_3$ type cold groundwater (SCGW) occurring in shallow peripheral parts of CTGW; and the intermediate type groundwater (STGW). CTGW waters are typical of thermal water in the area, because they have the highest outflow temperatures and contain very high concentrations of Na, K and $SiO_2$ due to the sufficient reaction with silicate minerals in deep reservoir. Their enriched $SO_4$ was likely formed by gypsum dissolution. The major ion composition of CTGW shows the general approach to a partial equilibrium state with rocks at depth. The application of various alkali ion geothermometers yields temperature estimates in the range of 88 to $198{\circ}C$ for the thermal reservoir. Multiple mineral equilibrium calculation indicates asimilar but narrower temperature range between about 100 and $155{\circ}C$. These temperature estimates are not significantly higher than the measured outflow temperatures for CTGW Considering the heat loss during the ascent- of thermal waters, this fact may suggest that a thermal reservoir in the study area is likely located at relatively shallow depths (possibly close to the depth of preexisting wells). Therefore, we suggest a high potential for geothermal energy development around the Bugok area in southern Korea.

• Nuclear Engineering and Technology
• /
• 제54권3호
• /
• pp.965-974
• /
• 2022

Platinum anodes are widely used for metal oxides reduction in LiCl-Li₂O, however high-cost and low-corrosion resistance hinder their implementation. NiO-Li₂O ceramics is an alternative corrosion resistant anode material. Anode processes on platinum and NiO-Li₂O ceramics were studied in (80 mol.%) LiCl-(20mol.%)KCl and (80 mol.%)LiCl-(20 mol.%)KCl-Li₂O melts by cyclic voltammetry, potentiostatic and galvanostatic electrolysis. Experiments performed in the LiCl-KCl melt without Li₂O illustrate that a Pt anode dissolution causes the Pt²⁺ ions formation at 3.14 V and 550℃ and at 3.04 V and 650℃. A two-stage Pt oxidation was observed in the melts with the Li₂O at 2.40 ÷ 2.43 V, which resulted in the Li₂PtO₃ formation. Oxygen current efficiency of the Pt anode at 2.8 V and 650℃ reached about 96%. The anode process on the NiO-Li₂O electrode in the LiCl-KCl melt without Li₂O proceeds at the potentials more positive than 3.1 V and results in the electrochemical decomposition of ceramic electrode to NiO and O₂. Oxygen current efficiency on NiO-Li₂O is close to 100%. The NiO-Li₂O ceramic anode demonstrated good electrochemical characteristics during the galvanostatic electrolysis at 0.25 A/cm² for 35 h and may be successfully used for pyrochemical treating of spent nuclear fuel.

• 콘크리트학회논문집
• /
• 제26권6호
• /
• pp.723-730
• /
• 2014

최근 고로슬래그 미분말의 사용량이 증가함에 따라 고로슬래그 미분말 혼입 시멘트의 수화반응 모델뿐만 아니라 압축강도, 수화생성물, 수화열 등 고로슬래그 미분말 혼입 시멘트 페이스트의 물성에 관한 연구가 활발히 진행되고 있다. 하지만 고로슬래그 미분말 혼입 시멘트 페이스트의 물성에 큰 영향을 끼치는 고로슬래그 미분말의 반응도에 대한 연구는 세계적으로도 부족하며 특히 국내에서는 전무한 실정이다. 따라서 본 연구는 선택적 추출법을 이용하여 시멘트 페이스트 내 고로슬래그 미분말의 반응도를 정량분석하고 물 바인더비, 치환율, 양생온도에 따라 압축강도, 화학결합수, $Ca(OH)_2$을 측정하여 비교 분석 하였다. 실험결과 시멘트 페이스트 내 고로슬래그 미분말의 반응도, 화학결합수, $Ca(OH)_2$은 치환율이 낮고 물 바인더비와 양생 온도가 높을수록 높게 나타났으며 특히 고로슬래그 미분말의 반응도는 최종적으로 약 0.3~0.4 값에 수렴하는 것으로 나타났다.

• 한국가스학회지
• /
• 제16권5호
• /
• pp.28-34
• /
• 2012

보일러 튜브용 크롬강의 열화기구에 대해 고찰하였다. 크롬강의 열화는 경도 및 응력-파단 수명의 변화를 동반하는데, 이는 주로 탄화물 분해 거동에 의존한다. 그런데 2Cr강인 T22의 열화는 이러한 탄화물 거동에 따르지만 12Cr강인 X20의 열화는 마르텐사이트 래쓰 성장거동에 따르기도 한다. T22와 X20의 열화에 의한 경도값과 응력-파단수명 변화현상을 미세조직적인 측면에서 고찰하였다.

• Corrosion Science and Technology
• /
• 제6권3호
• /
• pp.103-111
• /
• 2007

The effect of stress factors on the growing process of stress corrosion cracking (SCC) of the sensitized 18-8 stainless steel in high temperature water was investigated using equations of crack growth rate derived from applying electric circuits to SCC corrosion paths. Three kinds of cross sections have to be considered when electric circuit is constructed using total current. The first is ion flow passage area, $S_{sol}$, of solution in crack, the second is total dissolving surface area, $S_{dis}$, of metal on electrode of crack tip and the third is dissolving cross section, $S_{met}$, of metal on grain boundary or in base metal or in welding metal. Stress may affect each area. $S_{sol}$ may depend on applied stress, $\sigma_{\infty}$, related with crack depth. $S_{dis}$ is expressed using a factor of $\varepsilon(K)$ and may depend on stress intensity factor, K only. SCC crack growth rate is ordinarily estimated using a variable of K only as stress factor. However it may be expected that SCC crack growth rate depends on both applied stress $\sigma_{\infty}$ and K or both crack depth and K from this consideration.$\varepsilon(K)$ is expressed as ${\varepsilon}(K)=h_2{\cdot}K^2+h_3{\cdot}K^3$ when $h_{2}$ and $h_{3}$ are coefficients. Also, relationships between SCC crack growth rate, da/dt and K were simulated and compared with the literature data of JBWR-VIP-04, NRC NUREG-0313 Rev.2 and SKIFS Draft. It was pointed out in CT test that the difference of distance between a point of application of force and the end of starter notch (starting point of fatigue crack) may be important to estimate SCC crack growth rate. An anode dissolution current density was quantitatively evaluated using a derived equation.

• 한국결정성장학회지
• /
• 제17권3호
• /
• pp.95-101
• /
• 2007

수열합성 장치를 이용하여 종자 결정이 도포된 알루미나 지지체 위에 제올라이트 박막을 합성하였다. X-선 회절 분석과 전자현미경 사진을 이용하여 반응기 내에 생성된 제올라이트 A 분말과 제올라이트 A박막의 생성과 전이 생성물에 대해 합성온도, 합성시간, 종자결정의 영향에 대해서 고찰하였다. 제올라이트 A박막의 생성은 지지체 표면에 도포된 종자 결정에서 치밀한 연속적인 박막이 형성된 다음 용해과정을 거쳐 결정의 크기가 큰 다결정 층을 형성하고, 최종적으로 소다라이트를 거쳐 무정형으로 진행하였다. 반면에 분말에서는 반응초기부터 소다라이트가 관찰되는데 고정된 제올라이트 A 박막과 다르게 결정주위의 공간적인 차이에 의해 소다라이트가 생성하기에 용이한 공간을 갖기 때문에 소다라이트가 쉽게 생성되는 것으로 생각된다. 합성온도가 높으면 짧은 시간 내에 전이 생성물을 거쳐 무정형으로 진행하였고 온도가 낮으면 합성 시간이 길고 피복도가 다소 낮은 제올라이트 A 박막을 얻었다. $120^{\circ}C$, 12시간에서 피복도가 높은 치밀한 제올라이트 A박막을 합성하였다.

• Journal of Welding and Joining
• /
• 제31권3호
• /
• pp.76-83
• /
• 2013

This study investigated the effect of bonding temperature and holding time on microstructures and mechanical properties of diffusion bonded joint of Haynes230. The diffusion bonds were performed at the temperature of 950, 1050, and $1150^{\circ}C$ for holding times of 30, 60, 120 and 240 minutes at a pressure of 4MPa under high vacuum condition. The amount of non-bonded area and void observed in the bonded interface decreased with increasing bonding temperature and holding time. Cr-rich precipitates at the linear interface region restrained grain migration at $950^{\circ}C$ and $1050^{\circ}C$. However, the grain migration was observed in spite of short holding time due to the dissolution of precipitates to base metal in the interface region at $1150^{\circ}C$. Three types of the fracture surface were observed after tensile test. The region where the coalesce and migration of grain occurred much showed high fracture load because of base metal fracture whereas the region where those did less due to the precipitates demonstrated low fracture load because of interface fracture. The expected fracture load could be derived with the value of fracture area of base metal ($A_{BF}$) and interface ($A_{IF}$), $Load=201A_{BF}+153A_{IF}$. Based on this equation, strength of base metal and interface fracture were calculated as 201MPa and 153MPa, respectively.