• 전산구조공학
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• 제10권2호
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• pp.51-55
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• 1997

미래의 구조공학 자동화시스템은 Windows NT 운영체제의 저가의 데스크탑 컴퓨터에서 작동하며 객체지행적 CAD를 사용할 것이다. 모든 구조공학 관련 프로그램들은 객체지향 프로그램기법과 병렬처리기술로 재개발될 것이다. 구조공학 관련 소프트웨어프로그램의 통하븐 Microsoft사의 Objected Linking and Embedding(OLe)자동화 기술과 강력한 다중처리, 그리고 Windows NT의 다중연결 서버 기능에 의하여 이루어진다. 이 논문에서는 먼저 Windows NT의 다중연결 서버 기능에 의하여 이루어진다. 이 논문에서는 먼저 Windows NT 운영체제의 데스크탑 컴퓨터에서 구조공학 자동화시스템의 응용현황을 설명하고 미래의 구조공학 자동화 소프트웨어의 개발경향과 전략에 대해 논하게 될 것이다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제21권2호
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• pp.8-14
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• 2016

We compared the plausible reaction mechanism and quantitative efficiency of highly self-organized TiO₂ nanotube (ntTiO₂) film with TiO₂ powder. Film was fabricated by electrochemical potentiostatic anodization of titanium thin film in an ethylene-glycol electrolyte solution containing 0.3 wt% NH₄F and 2 vol% deionized water. Nanotubes with a pore size of 80-100 nm were formed by anodization at 60 V for 3 h. Humic acid (HA) was degraded through photocatalytic degradation using the ntTiO₂ film. Pseudo first-order rate constants for 0.3 g of ntTiO₂, 0.3 g TiO₂ powder, and 1 g TiO₂ powder were 0.081 min⁻¹, 0.003 min⁻¹, and 0.044 min⁻¹, respectively. HA adsorption on the ntTiO₂ film was minimal while adsorption on the TiO₂ powder was about 20% based on thermogravimetric analysis. Approximately five-fold more normalized OH radicals were generated by the ntTiO₂ film than the TiO₂ powder. These quantitative findings explain why ntTiO₂ film showed superior photocatalytic performance to TiO₂ powder.

• Bulletin of the Korean Chemical Society
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• 제32권11호
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• pp.4035-4040
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• 2011

Long $TiO_2$ nanotube (NT) arrays, prepared by electrochemical anodization of Ti foils, have been utilized as dye-adsorbing electrodes in dye-sensitized solar cells (DSCs). By anodizing for 1-24 hr and subsequent annealing, highly crystallized and tightly-adhered NT arrays were tailored to 11-150 ${\mu}m$ lengths, ~90 nm innerpore diameter and ~30 nm wall thickness. I-V curves revealed that the photovoltaic conversion efficiency (${\eta}$) was proportional to the NT length up to 36 ${\mu}m$. Beyond this length, the ) was proportional to the NT length up to ${\eta}$ was still steadily increased, though at a much lower rate. For example, an ${\eta}$ of 5.05% at 36 ${\mu}m$ was increased to 6.18% at 150 ${\mu}m$. Transient photoelectron spectroscopic analyses indicated that NT array-based DSCs revealed considerably higher electron diffusion coefficient ($D_e$) and life time (${\tau}_e$) than those with $TiO_2$ nanoparticles (NP). Moreover, the electron diffusion lengths ($L_e$) of the photo-injected electrons were considerably larger than the corresponding NT lengths in all the cases, suggesting that electron transport in NT arrays is highly efficient, regardless of tube length.

• Journal of Electrochemical Science and Technology
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• 제1권2호
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• pp.92-96
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• 2010

A new synthesis method for the preparation of Pt electrocatalysts on carbon nanofibers (CNFs) is reported. In this method, Pt electrocatalysts are loaded onto 2-naphthalenethiol (NT) functionalized CNFs. The noncovalent functionalization of CNFs by NT is the effective way for better distribution of Pt particles and higher electrocatalytic activity in polymer electrolyte membrane fuel cells. It was found that the presence of NT acts as a poison to catalysts. Therefore, it is necessary to remove NT through the heat treatment at $400^{\circ}C$.

• 한국수정란이식학회지
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• 제10권1호
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• pp.73-82
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• 1995

large scale production of cloned embryos requires the technology of multiple generation nuclear transplantation(NT) using NT embryos as the subsequent donor nuclei. The purposes of this study were producing the second generation cloned rabbit embryos, and also to determine the electrofusion rate and in vitro developmental potential comparatively in the cloned embryos of the first and second NT generation. The embryos of 16-cell stage were collected from the mated does by flushing oviducts with Dulbecco's phosphate buffered saline(D-PBS) containing 10% fetal calf serum(FCS) at 47 hours after hCG injection In the first generation NT, the nuclear donor embryos were synchronized in the phase of Gi /S transition of 32-cell stage. The first generation NT embryos which were developed to 8-cell were synchronized in Gi /S transition phase of the following 16-cell stage and used as donor nuclei for second generation Synchronization of the cell cycle of blastomeres was induced, first, using an inhibitor of microtuble polymerization, colcemid for 10 hours to arrest blastomeres in M phase, and secondly, using a DNA synthesis inhibitor, aphidicolin for 1.5 to 2 hours to arrest them in Gi /S transition boundary. The recipient cytoplasms were obtained by removing the nucleus and the first polar body from the oocytes collected at 14 hours after hCG injection. The separated donor blastomeres were injected into the enucleated recipient oocytes by micromanipulation and were electrofused by electrical stimulation of three pulses for 60 $\mu$sec at 1.25 kV /cm in 0.28 M rnannitol solution The fused oocytes were co-cultured with a monolayer of rabbit oviductal epithelial cells in M-199 solution containing 10% FCS for 120 hours at 39$^{\circ}C$ in a 5% $CO_2$ incubator. Following in vitro culture of the first and second generation cloned embryos to blastocyst stage, they were stained with Hoechst 33342 dye for counting the number of blastomeres by fluorescence microscopy. The results obtained were summarized as follows: 1. The electrofusion rate was found to be similar as 79.4 and 91.5% in the first and second generation NT rabbit embryos, respectively. 2. The in vitro developmental potential to blastocyst stage of the second generation NT embryos (23.3%) was found significantly(p<0.05) lower, compared with that of the first generation NT embryos (56.8%). 3. The mean blastomeres counts of embryos developed to blastosyst stage following in vitro culture for 120 hours and also their daily cell cycles during the culture period were decreased significantly (p<0.05) to 104.3 cells and 1.33 cylces in the second NT generation, compoared with 210.4 cells and 1.54 cycles in the first NT generation, respectively.

• 수산해양기술연구
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• 제47권2호
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• pp.128-138
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• 2011

In this study, energy budget was estimated to produce an efficient artificial seed. And it needs to enhance fisheries productivity of sandfish, A. japonicus. In order to estimate energy budget of the sandfish, A. japonicus juvenile fed on nonriched Artemia nauplii (NA) and the enriched Artemia nauplii (EA), of sandfish were reared at constant condition of seawater temperature of natural temperature (NT) and heated temperature (HT). During the reared period, energy used by the reared juveniles were calculated from estimates of data on ingestion, growth, oxygen consumption, nitrogen excretion and energy content. Energy budget of NT-NA, NT-EA, HT-NA and HT-EA were represented as 100C=66.49G+21.28M+0.78F+1.44U, 100C=67.54G+21.40M+9.39F+1.67U, 100C=66.86G+22.66M+8.01F+2.47U and 100C=67.06G+22.96M+7.70F+2.28U. The assimilation efficiency estimated NT-NA, NT-EA, HT-NA and HTEA were represented as 87.78%, 88.94%, 89.52% and 90.02%. Gross growth efficiency estimated NT-NA, NT-EA, HT-NA and HT-EA were represented as 66.49%, 67.54%, 66.86% and 67.06%. Net growth efficiency estimated NT-NA, NT-EA, HT-NA and HT-EA were represented as 75.75%, 75.94%, 74.68% and 74.49%. In this results, two ways could be considered to produce an efficient artificial seed of sandfish. To hasten the growth of sandfish juvenile, heated seawater (HT) and enriched Artemia nauplii (EA) should be inputted to reared condition. And to increase the energy efficiency, natural seawater (NT) and enriched Artemia nauplii (EA) should be inputted to reared condition.

• 한국컴퓨터정보학회논문지
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• 제19권2호
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• pp.11-19
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• 2014

본 논문에서는 노후화된 NT 서버를 중심으로 서버 통합 가상화를 구축하고 이에 따른 효과 분석을 통해 다음과 같은 결과를 제시하였다. 첫째, 다수의 물리적인 서버를 가상화 통합 서버에 탑재하여 전산 데이터 센터의 상면공간확보로 인한 항온항습기의 효율 증가를 얻을 수 있었다. 둘째, 노후화된 대형서버의 가상화 탑재로 전력 사용량 감소 및 신규 서버도입에 따른 추가 하드웨어 도입감소로 전산데이터센터 유지비용과 신규 자원 도입에 따른 비용 절감 효과를 도출할 수 있었다. 상면 절감 효과는 89%, 전력과 냉방 소비량은 기존 대비 79% 정도 절감 효과를 얻었다. 이러한 NT 서버 통합 가상화는 현재 뿐만 아니라 추후에도 전산센터의 유지보수 비용을 주는데 기여하고 Green-IT로의 변화를 기대 할 수 있다. 본 논문에서 적용한 가상화 서버 통합 구축 방법은 UNIX 계열 및 기타 다른 서버군을 통합 할 때도 동일하게 적용할 수 있다.

• 한국정보과학회논문지:컴퓨팅의 실제 및 레터
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• 제5권2호
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• pp.176-184
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• 1999

지금까지의 소프트웨어 기반 분산 공유 메모리(이하 DSM이라 칭함)시스템은 유닉스 워크스테이션 클러스터를 목표로 하는 것이 대부분이었다. 그러나 현재 Windows-NT 는 서버급 시스템과 PC 모두를 위한 운영체제로서 유닉스와 더불어 널리 사용되고 있는 실정이다. 본 논문에서는 Windows-NT 워크스테이션 클러스터 환경을 위한 DSM 시스템을 구현하고, 구현된 DSM 시스템의 성능 평가 결과를 제시한다. 구현된 DSM 시스템은 Win32 API와 표준 실행-시간 라이브러리를 이용해 구현되었기 때문에 모든 Windows-NT 워크스테이션에서 실행 가능하며 , 프로그래머는 몇 라인의 코드 추가만으로 DSM 시스템 상에서 수행되는 병렬 응용 프로그램을 작성할 수 있다. 워크스테이션 간의 상호연결망으로 범용성을 위해 이더넷 LAN을 지원하였고, 아울러 성능 향상을 위해 기가비트 SAN(System Area Network)도 지원하였다. 기가비트 SAN을 위한 하드웨어로는 Dolphin 사의 PCI-SCI 타입 제품인 Clustar를 사용하였다. 우리는 성능 평가를 통해, 구현된 DSM 시스템이 정확히 동작함은 물론 확장성이 뛰어나다는 것을 확인하였다. 특히 , 기가비트 SAN을 사용할 경우 일부 병렬 벤치 마크 프로그램에서는 노드 수 증가에 따라 성능이 거의 선형적으로 향상된다는 것을 알 수 있었다. 본 논문이 기여하는 바는 Windows-NT 기반 소프트웨어 DSM 시스템의 원천 기술을 확보함으로써 향후 Windows-NT 워크스테이션 클러스터 환경에서의 분산 및 병렬 처리 연구에 도움을 줄 수 있다는 점이다.

• Molecules and Cells
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• 제24권3호
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• pp.323-328
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• 2007

SOX (Sry-related HMG box) family proteins, which have an evolutionarily conserved DNA binding domain, have crucial roles in cell differentiation. However, their target genes remain enigmatic. Some members of the SOX family may have roles in regulation of cell proliferation. We established stable NT2/D1 cell lines overexpressing SOX15 (SOX15-NT2/D1), and a modified 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay showed that the SOX15-NT2/D1 cells exhibited significantly slower growth than the controls. Flow cytometry analysis revealed that an increased fraction of the SOX15-NT2/D1 cells were in G1-G0. In addition, a microarray analysis identified 26 genes that were up-regulated in the SOX15-NT2/D1 cells, but none that were down-regulated genes. Among the up-regulated genes, IGFBP5, S100A4, ID2, FABP5, MTSS1, PDCD4 have been shown to be related to cell proliferation and/or the cell cycle.

• 한국응용곤충학회지
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• 제37권2호
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• pp.187-191
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• 1998

새로운 Bacillus thuringiensis NT0423균주를 이용한 배양체계를 확립하고 대량생산을 위한 새로운 배양배지를 개발하였다 대두박과 밀기울의 다양한 성분비로 구성된 5종의 SW 배지는 기존의 인공합성배지인 GYS나 LB B. huringiensis 의 성장과 포자형성면에서 훨씬 우수한 결과를 보였고, 그중 대두박과 밀기율이 3:2의 비율로 구성된 SW32배지에서 전체 세포수가 3.9$\times$${10}^{8}$CFU/ml에 달했고, 대부분의 세포가 빠르게 포자를 형성하여 (3.7$\times$${10}^{8}$CFU/ml)가장 효율적이었다. 배양에 따른 배지의 pH는 최저 6.2에서 최고 7.3까지 변화하여 성장에 크게 영향을 미치지 않았고, 전체 배양액에서 대두박과 밀기울이 차지하는 비율이 4%일 경우, ml당 4.2$\times$${10}^{8}$CFU/ml의 포자가 형성되어 B. thuringiensis 의 성장에 가장 유리하였다. 교반플라스크와 5ι의 소규모 발효기를 이용한 B. thuringiensis 의 배양조건 확립에 의해 각각 최대 1$\times$${10}^{9}$CFU/ml과 5$\times$${10}^{10}$CFU/ml에 해당하는 많은 양의 균체를 회수할 수 있다.