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준설토 배송관로 내에서의 개질재 혼합효율에 대한 CFD 해석
박병준,강병윤,정민철,신재렬,Park, Byongjun,Kang, Byungyoon,Chung, Minchul,Shin, Jaeryul 대한토목학회 2015 대한토목학회논문집 Vol.35 No.5
본 연구는 준설매립과정에서의 관중혼합 거동을 3차원 전산유체역학(CFD, Computational Fluid Dynamics)을 통해 분석한 연구로 준설토 배송관과 개질재 주입관이 합류하며 발생되는 이상(2-phase)유체의 혼합효율을 사전 평가함으로써 관중혼합 양상을 고찰하는 물리실험의 시행착오를 줄여 경제성을 증진시키는데 연구목적을 두고 있다. 수치해석에 이용된 CFD 코드는 OpenFOAM$^{(R)}$이고, 몇 가지의 기본가정 하에 배송관-주입관의 관경과 합류각을 변화시켜 총 18가지 경우에 대한 삼상(3-phase)유체 거동을 모의하였다. 그 결과 혼합효율에 대한 우열은 있었으나 그 차이는 미미하였고, 모든 경우에서 각 재료 사이의 경계층이 뚜렷하게 형성되었다. 이러한 현상을 극복하기 위한 보완 실험을 통해 경계층 파쇄(破碎)를 위한 관 내 부속 구조물이 고안되었으며, 본 연구에서 제시된 구조물은 단거리 배송관로 내 준설토와 개질재의 혼합효율을 크게 향상시킬 수 있음을 확인할 수 있었다. This study utilised Computational Fluid Dynamics(CFD) for preliminary assessment of mixing efficiencies of 2-phase fluids in a pipe at which a slurry flow and an injected solidifier join, for the purposes of reducing trial-and-error-based instances of physical experiments and conducting the overall research in an economical way. Using OpenFOAM$^{(R)}$, we simulated behavior of 3-phase fluids under 18 different settings generated by changing diameters of a dredged soil transportation pipe, a quality improving material injection pipe and the confluence angle. While difference in mixing efficiencies amongst the instances was insignificant, discernible boundary layers amongst the materials were observed in all of the instances. In order to break the boundary layers, we designed a substructure inside a pipe and found out that it could remarkably improve mixing efficiencies particularly for short distance applications.
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PEMFC 전극촉매 Pt/C와 PtCo/C의 촉매 지지체 열화비교
오소형,한유한,정민철,유동근,박권필,Sohyeong Oh,Yoohan Han,Minchul Chung,Donggeun Yoo,Kwonpil Park 한국화학공학회 2023 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.61 No.3
In PEMFC, PtCo/C alloy catalysts are widely used because of good performance and durability. However, few studies have been reported on the durability of carbon supports of PtCo/C evaluated at high voltages (1.0~1.5 V). In this study, the durability of PtCo/C catalysts and Pt/C catalysts were compared after applying the accelerated degradation protocol of catalyst support. After repeating the 1.0↔1.5V voltage change cycles, the mass activity, electrochemical surface area (ECSA), electric double layer capacitance (DLC), Pt dissolution and the particle growth were analyzed. After 2,000 cycles of voltage change, the current density per catalyst mass at 0.9V decreased by more than 1.5 times compared to the Pt/C catalyst. This result was because the degradation rate of the carbon support of the PtCo/C catalyst was higher than that of the Pt/C catalyst. The Pt/C catalyst showed more than 1.5 times higher ECSA reduction than the PtCo/C catalyst, but the corrosion of the carbon support of the Pt/C catalyst was small, resulting in a small decrease in I-V performance. In order to improve the high voltage durability of the PtCo/C catalyst, it was shown that improving the durability of the carbon support is essential.
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비피리미딘계 배위자를 골격으로 하는 Pt(II)착체의 합성 및 특성
손석환 ( Seokhwan Son ),안호근 ( Hogeun Ahn ),정민철 ( Minchul Chung ) 한국화학공학회 2016 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.54 No.4
In this study, new platinum complexes were synthesized utilizing the ligand of a 2,2``-bispyrimidine (bpim), 2,2``-bipyridine (bpy), 5,5``-dimethyl-2,2``-bipyridine (5,5-mebpy), 5``-bromo-2,2``-bipyridine (5-brbpy), 5,5``-dibromo-2,2``-bipyridine (5,5-brbpy), 4,4``-dimethyl-2,2``-bipyridine (4,4-mebpy), 4,4``- dihexyl-2, 2``-Bipyridine (4,4-hebpy), 1,10``-Phenanthroline (phen), 3, 4, 7, 8``-tetramethyl-1, 10``-Phenanthroline (3,4,7,8-phen). In order to determine chemical structure of Synthesized platinum complexes, 1H(13C)-NMR, UV-vis and FT-IR were used and optical physics and chemical properties were measured PL. In the case of platinum complexes, wavelength has been identified 356~421 nm. Quantum efficiency in DMSO solution was appeared 0.05~0.46.
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이승민 ( Seungmin Lee ),손석환 ( Seokhwan Son ),정성훈 ( Sunghun Jung ),곽원봉 ( Wonbong Kwak ),신은주 ( Eun Ju Shin ),안호근 ( Hogeun Ahn ),정민철 ( Minchul Chung ) 한국공업화학회 2018 공업화학 Vol.29 No.1
Styrenated phenol alkoxylate (SP-A)는 일반적으로 균일계 염기 촉매 하에서 styrenated phenol (SP)과 ethylene oxide (EO)로부터 제조되어진다. 그러나, 취급이 용이하지 않은 EO를 사용하려면 고압반응장치를 이용한 반응공정 제어가 필요하다. 또한, 균일계 염기 촉매를 사용하면 반응종결 후에 잔존하는 염기를 제거하기 위한 중화공정이 필요하고, 촉매와 생성물의 분리가 어렵다는 문제점이 있다. 따라서, 본 연구에서는 균일계 염기 촉매를 사용하지 않고 불균일계염기 촉매를 사용하여 SP와 ethylene carbonate (EC)의 반응으로부터 제조된 SP-A에 대하여 보고하고자 한다. SP-A의 제조에 사용된 불균일계 염기 촉매는 KOH를 La<sub>2</sub>O<sub>3</sub>에 담지시킨 후, 소성하여 얻었다. 또한, EO 대신 EC를 사용함으로써 고압반응이 아닌 상압반응 조건에서 SP-A제조가 가능하였다. 합성된 SP-A의 평균 분자량 크기는 반응조건에 따라서 매우 다양하게 나타났다. KOH/La<sub>2</sub>O<sub>3</sub>촉매 하에서 제조된 SP-A의 평균 분자량 크기는 반응온도, 촉매의 첨가량 및 EC의 첨가량을 조절함으로써 임의로 조절이 가능하였다. Styrenated phenol alkoxylates (SP-A) were prepared from styrenated phenol (SP) and ethylene oxide (EO) under a homogeneous base catalyst. However, to use EO that is difficult to handle, a high-pressure reaction device capable of controlling the reaction process should be used. Additionally, when a homogeneous base catalyst is used, a neutralization process is required to remove residual bases after the reaction, and it is also difficult to separate the catalyst and the product. Therefore, in this study, we report the results of SP-A prepared from the reaction of SP and EC using only heterogeneous base catalysts. The heterogeneous base catalyst was obtained by supporting KOH on La<sub>2</sub>O<sub>3</sub> and calcintion. Using EC instead of EO, it was possible to produce SP-A under the atmospheric rather than high-pressure reaction condition. Average molecular weights of synthesized SP-A varied greatly depending on reaction conditions. The average molecular weight of SP-A prepared using the KOH/La<sub>2</sub>O<sub>3</sub> catalyst could be controlled arbitrarily by controlling the reaction temperature and added catalyst and EC amounts.
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정민철,정혜성,김성민,이정훈,박권필,안호근 한국공업화학회 2005 응용화학 Vol.9 No.1
We have been used for the Pt catalyst of cathode electrode in fuel cell. Weak point of Pt electrode are easily deactivated by the CO poisoning which are producing in reaction at electrode. Recent, researchers have developed cathode electrode to avoid the CO poisoning in electrode using the Pt-alloy or another novel metal. We now report Au-carbene complexes as an Au-electrode precursor derived from the reaction of the carbene with the ClAu(PPh₃) complex in THF/MeOH.
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