• 미생물학회지
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• 제38권2호
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• pp.119-126
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• 2002

심해와 연안의 서로 다른 해양퇴적토 환경에서 ATP농도를 이용한 총 미생물 생체량을 측정하였다. 표층 ATP의 분포는 연안역에서 가장 높았으며, 육지로부터 멀어질수록 감소하였다. 또한 수직적으로는 깊이에 따라 급격히 감소하는 양상을 나타내, 저층의 생태계가 수층으로 부터의 영양원 공급에 의해 일차적으로 조절되고 있는 것으로 나타났다. 한편, 유기물은 퇴적물로의 흡착으로 인해 환경 내 체류시간이 길어짐으로 인해, 유기탄소의 함량 변화가 ATP에 비해 급격히 일어나지 않았으며, 특히, 연안퇴적토의 경우 유기탄소의 함량 변화에 비해 ATP의 농도변화가 일정하게 나타나 두 변수간의 유의성 이 없는 것으로 나타났다. 이러한 결과는 분해가능한 유기물의 공급이 많은 연안퇴적토의 경우, 영양원에 의한 조절보다는 상위영양단계의 포식활동이 미생물의 생체량을 최종적으로 조절하는 요인으로 작용하기 때문 인 것으로 사료된다. 지역분포 특성 및 수직적 분포 특성으로부터 ATP는 서로 다른 저서 생태환경의 생체량 분석을 위한 일차적 인 도구로 유용하게 쓰일 수 있는 것으로 나타났다.

• Journal of Microbiology and Biotechnology
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• 제23권4호
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• pp.511-517
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• 2013

In this work, a fibrous bed bioreactor with high specific surface area and good adsorption efficacy for S. cerevisiae cells was used as the immobilization matrix in the production of ethanol. In batch fermentation, an optimal ethanol concentration of 91.36 g/l and productivity of 4.57 g $l^{-1}\;h^{-1}$ were obtained at an initial sugar concentration of 200 g/l. The ethanol productivity achieved by the immobilized cells was 41.93% higher than that obtained from free cells. Ethanol production in a 22-cycle repeated batch fermentation demonstrated the enhanced stability of the immobilized yeast cells. Under continuous fermentation in packed-bed reactors, a maximum ethanol concentration of 108.14 g/l and a productivity of 14.71 g $l^{-1}\;h^{-1}$ were attained at $35^{\circ}C$, and a dilution rate of 0.136 $h^{-1}$ with 250 g/l glucose.

• 한국수자원학회논문집
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• 제49권9호
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• pp.741-748
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• 2016

개착식 하상여과에 대해서 실험실 규모의 모형을 구축하고 중사, 왕사, 화산석, 자갈에 대한 단일 여재를 구성하였다. 실험을 통해 투수계수 및 하상 여과에 대한 취수량을 추정하고, 지하수 유동 모델링인 Visual MODFLOW를 통해 탁도 변화에 따라 수정된 투수계수를 적용하고 미치는 영향을 분석하였다. 각 여재마다 22개의 수정 투수계수 시나리오가 적용되었다. 전체 모델링에서 최소 오차는 화산석(2~5 mm)을 여재로 한 경우 상부에서부터 3개 지층에 대해서 20% 감소된 투수계수를 적용한 시나리오다. 이는 화산석의 특성상 탁도를 유발하는 황토가 여재에 흡착되어 상부에서 3번째 지층까지 영향을 미치는 것으로 추정되었다. 또한 입자의 크기가 작은 중사의 경우 5% 감소된 투수계수를 상부에서 두 번째 지층까지 적용한 시나리오에서도 작은 오차 값을 나타냈다.

• Journal of Electrochemical Science and Technology
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• 제1권1호
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• pp.31-38
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• 2010

In this study, we have demonstrated the fine structure effect of PdCo electrocatalyst on oxygen reduction reaction activity with different alloy composition and heat-treatment time. In order to identify the intrinsic factors for the electrocatalytic activity, various X-ray analyses were used, including inductively coupled plasma-atomic emission spectrometer, transmission electron microscopy, X-ray diffractometer, and X-ray Absorption Spectroscopy technique. In particular, extended X-ray absorption fine structure was employed to extract the structural parameters required for understanding the atomic distribution and alloying extent, and to identify the corresponding simulated structures by using FEFF8 code and IFEFFIT software. The electrocatalytic activity of PdCo alloy nanoparticles for the oxygen reduction reaction was evaluated by using rotating disk electrode technique and correlated to the change in structural parameters. We have found that Pd-rich surface was formed on the Co core with increasing heating time over 5 hours. Such core shell structure of PdCo/C showed that a superior oxygen reduction reaction activity than pure Pd/C or alloy phase of PdCo/C electrocatalysts, because the adsorption energy of adsorbates was apparently reduced by lowering the dband center of the Pd skin due to a combination of the compressive strain effect and ligand effect.

• Carbon letters
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• 제21권
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• pp.33-50
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• 2017

In this study, Fe-Ni bimetallic catalyst supported on kaolin is prepared by a wet impregnation method. The effects of mass of kaolin support, pre-calcination time, pre-calcination temperature and stirring speed on catalyst yields are examined. Then, the optimal supported Fe-Ni catalyst is utilised to produce multi-walled carbon nanotubes (MWCNTs) using catalytic chemical vapour deposition (CCVD) method. The catalysts and MWCNTs prepared using the optimal conditions are characterized using high resolution transmission electron microscope (HRTEM), high-resolution scanning electron microscope (HRSEM), electron diffraction spectrometer (EDS), selected area electron diffraction (SAED), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET), and X-ray diffraction (XRD). The XRD/EDS patterns of the prepared catalyst confirm the formation of a purely crystalline ternary oxide ($NiFe_2O_4$). The statistical analysis of the variance demonstrates that the combined effects of the reaction temperature and acetylene flow rate predominantly influenced the MWCNT yield. The $N_2$ adsorption (BET) and TGA analyses reveal high surface areas and thermally stable MWCNTs. The HRTEM/HRSEM micrographs confirm the formation of tangled MWCNTs with a particle size of less than 62 nm. The XRD patterns of the MWCNTs reveal the formation of a typical graphitized carbon. This study establishes the production of MWCNTs from a bi-metallic catalyst supported on kaolin.

• 한국세라믹학회지
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• 제53권6호
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• pp.604-609
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• 2016

This study reports on wet-foam stability with respect to porous ceramics from a particle-stabilized colloidal suspension that is achieved through the addition of polymethyl methacrylate (PMMA) using a wet process. To stabilize the wet foam, an initial colloidal suspension of $Al_2O_3$ was partially hydrophobized by the surfactant propyl gallate (2 wt.%) and $SiO_2$ was added as a stabilizer. The influence of the PMMA content on the bubble size, pore size, and pore distribution in terms of the contact angle, surface tension, adsorption free energy, and Laplace pressure are described in this paper. The results show a wet-foam stability of more than 83%, which corresponds to a particle free energy of $2.7{\times}10^{-12}J$ and a pressure difference of 61.1 mPa for colloidal particles with 20 wt.% of PMMA beads. It was possible to control the uniform distribution of the open/closed pores by increasing the PMMA content and by adding thick struts, leading to the achievement of a higher-stability wet foam for use in porous ceramics.

• Korean Chemical Engineering Research
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• 제49권6호
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• pp.739-744
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• 2011

선택적환원 반응용 활성탄 촉매는 액정디스플레이 제조 공정에서 배출되는 붕소를 포함하는 배가스 중의 $NO_x$를 제거하는데 사용되는데, 붕소가 촉매의 세공을 막거나 활성점에 침적되어 촉매 비활성화가 발생하게 된다. 폐촉매는 다양한 계면활성제를 포함하는 수용액 중에서의 세정, 건조 및 소성에 의해 재생이 가능하였다. 세정 과정의 조건, 계면 활성제 종류, 소성 조건 등을 변화시키면서 재생 전과 후의 폐촉매의 물리화학적 성능 비교를 위하여 질소 흡착 실험, ICP에 의한 원소 분석을 수행하였다. 암모니아를 사용하는 선택적환원 반응은 고정층 촉매 반응기를 사용하여 $120^{\circ}C$에서 수행하였다. $90^{\circ}C$의 수용액에서 비이온 계면활성제를 사용하여 세정하고, 질소 분위기에서 $550^{\circ}C$에서 소성하여 재생한 활성탄 촉매는 붕소가 가장 많이 제거되어 신규 활성탄과 유사한 수준의 표면적과 $NO_x$ 제거 효율을 회복하였다.

• Bulletin of the Korean Chemical Society
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• 제31권4호
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• pp.901-904
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• 2010

Decylthiocyanate (DTC) self-assembled monolayers (SAMs) on Au(111) were prepared by solution and vapor phase deposition methods at $50^{\circ}C$ for 24 h. The formation and surface structure of DTC SAMs were examined using scanning tunneling microscopy (STM). STM imaging revealed that DTC SAMs formed in 1 mM ethanol solution at $50^{\circ}C$ were composed of small ordered domains with lateral dimensions of a few nanometers and disordered phases, whereas DTC SAMs formed in the vapor phase at $50^{\circ}C$ contained two ordered phases: a closely packed c($4{\times}2$) superlattice and a striped phase with an interstripe spacing of 2.6 - 2.8 nm. It was also found that the ordered domain and vacancy island formation for DTC SAMs on Au(111) differs significantly from that of decanethiol SAMs, suggesting that adsorption mechanism is different from each other. From this study, it was confirmed that DTC SAMs with a high degree of structural order can be obtained by vapor phase deposition.

• 한국자기학회지
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• 제9권2호
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• pp.121-126
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• 1999

친수성 철계 자성유체의 제조와 이 자성유체를 Nd-영구자석과 병용하여 기름 밀봉 장치의 개발을 목적으로 실험검토한 결과 다음과 같은 결론을 얻었다. 1)평균 입경 100$\AA$, 자화값 125.5emu/g, 대기중 15$0^{\circ}C$까지 산화 변질성이 없는 실리카 피착 철 초미립자의 표면에 오레인산 이온, D.B.S. 이온 및 T.M.A. 이온을 흡착한 후 ethylene glycol 용액중에 분산시켜 친수성 철 분말 자성유체를 제조할 수 있었다. 2)이상의 친수성 철 분말 자성유체[70%(g/ )Fe]를 영구자석(3200 Gauss)과 병용하여 기름 밀봉 장치에 응용한 결과 영구자석의 설치 개수를 영구자석 6단 그리고 구동축과 밀봉 장치 사이 간격 0.2mm의 조건에서 압력 7400g/$\textrm{cm}^2$까지 견딜 수 있는 우수한 내압 특성을 얻었다.

• Bulletin of the Korean Chemical Society
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• 제33권4호
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• pp.1135-1140
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• 2012

An electrochromatographic microchip with carboxyl-group-derivatized mono-disperse silica packing was prepared from the corresponding colloidal silica solution by utilizing capillary action and self-assembly behavior. The silica beads in water were primed by the capillary action toward the ends of cross-patterned microchannel on a cyclic olefinic copolymer (COC) substrate. Slow evaporation of water at the front of packing promoted the self-assembled packing of the beads. After thermally binding a cover plate on the chip substrate, reservoirs for sample solutions were fabricated at the ends of the microchannel. The packing at the entrances of the microchannel was silver coated to fix utilizing an electroless silver-plating technique to prevent the erosion of the packed structure caused by the sudden switching of a high voltage DC power source. The electrochromatographic behavior of the microchip was explored and compared to that of the microchip with bare silica packing in basic borate buffer. Electrophoretic migration of Rhodamine B was dominant in the microchip with the carboxyl-derivatized silica packing that resulted in a migration approximated twice as fast, while the reversible adsorption was dominant in the bare silica-packed microchip. Not only the faster migration rates of the negatively charged FITC-derivatives of amino acids but also the different migration due to the charge interaction at the packing surface were observed. The electrochromatographic characteristics were studied in detail and compared with those of the bare silica packed microchip in terms of the packing material, the separation potential, pH of the running buffer, and also the separation channel length.