• Title/Summary/Keyword: E-64

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The Measurement of Combustible Properties of Cyclohexanol (사이클로헥산올의 연소특성치의 측정)

  • Ha, Dong-Myeong
    • Fire Science and Engineering
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    • v.28 no.2
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    • pp.64-68
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    • 2014
  • For the safe handling of cyclohexanol, this study was investigated the explosion limits of cyclohexanol in the reference data. The flash points and auto-ignition temperatures (AITs) by ignition delay time were experimented. The lower flash points of cyclohexanol by using closed-cup tester were experimented in$60^{\circ}C{\sim}64^{\circ}C$. The lower flash points of cyclohexanol by using open cup tester were experimented in $66^{\circ}C{\sim}68^{\circ}C$. This study measured relationship between the AITs and the ignition delay times by using ASTM E659 tester for cyclohexanol. The AIT of cyclohexanol was experimented as $297^{\circ}C$. The lower explosion limit (LEL) and the upper explosion limit UEL) by the measured the lower flash point and the upper flash point of cyclohexanol were calculated as 0.95 Vol% and 10.7 Vol%, respectively.

Mean ergodic theorem and multiplicative cocycles

  • Choe, Geon H.
    • Bulletin of the Korean Mathematical Society
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    • v.33 no.1
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    • pp.57-64
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    • 1996
  • Let $(X, B, \mu)$ be a probability space. Then we say $\tau : X \to X$ is a measure-preserving transformation if $\mu(\tau^{-1} E) = \mu(E)$. and we call it an ergodic transformation if $\mu(\tau^{-1}E\DeltaE) = 0$ for a measurable subset E implies $\mu(E) = 0$. An equivalent definition is that constant functions are the only $\tau$-invariant functions.

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Expressional Subpopulation of Cancers Determined by G64, a Co-regulated Module

  • Min, Jae-Woong;Choi, Sun Shim
    • Genomics & Informatics
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    • v.13 no.4
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    • pp.132-136
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    • 2015
  • Studies of cancer heterogeneity have received considerable attention recently, because the presence or absence of resistant sub-clones may determine whether or not certain therapeutic treatments are effective. Previously, we have reported G64, a co-regulated gene module composed of 64 different genes, can differentiate tumor intra- or inter-subpopulations in lung adenocarcinomas (LADCs). Here, we investigated whether the G64 module genes were also expressed distinctively in different subpopulations of other cancers. RNA sequencing-based transcriptome data derived from 22 cancers, except LADC, were downloaded from The Cancer Genome Atlas (TCGA). Interestingly, the 22 cancers also expressed the G64 genes in a correlated manner, as observed previously in an LADC study. Considering that gene expression levels were continuous among different tumor samples, tumor subpopulations were investigated using extreme expressional ranges of G64-i.e., tumor subpopulation with the lowest 15% of G64 expression, tumor subpopulation with the highest 15% of G64 expression, and tumor subpopulation with intermediate expression. In each of the 22 cancers, we examined whether patient survival was different among the three different subgroups and found that G64 could differentiate tumor subpopulations in six other cancers, including sarcoma, kidney, brain, liver, and esophageal cancers.

Optimization of I layer bandgap for efficient triple junction solarcell by ASA simulation (삼중접합 태양전지에서 Intrinsic Layer 밴드갭 가변을 통한 태양전지 고효율화 시뮬레이션)

  • Kang, Minho;Jang, Juyeon;Baek, Seungsin;Yi, Junsin
    • 한국신재생에너지학회:학술대회논문집
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    • 2011.11a
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    • pp.64.1-64.1
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    • 2011
  • 다중접합 태양전지는 흡수대역이 다른 juntion으로 구성되어, 각각의 태양전지 간의 전류정합(current matching)이 효율 향상에 중요하다. 본 실험에서는 Top cell에 i-a-Si:H(Thinckness:100nm), Middle cell에는 i-a-SiGe:H(Thickness:800nm)을 적용하였고, bottom cell에는 i-${\mu}c$-Si:H(Thickness:1800nm), 수광부의 p-layer에 에 SiOx을 이용하여 triple juntion amorphous silicon solar cell(삼중접합태양전지)을 구현하였다. 이를 최적화 시키기 위해 ASA simulation을 이용하여 각 Cell의 intrinsic layer의 밴드갭을 가변하였다. 가변 결과 i-a-Si:H : 1.85 eV, i-a-SiGe:H: 1.6 eV, i-${\mu}c$-Si:H: 1.4 eV에서 태양전지 효율 14.5 %을 기록 하였다. 본 연구를 통해 Triple juntion cell에서의 intrinsic layer의 밴드갭 최적화를 구현해 볼 수 있었다.

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Isolation of endosulfan degrading bacteria and their degradation characteristics (유기염소계 농약 endosulfan을 분해하는 미생물의 분리 및 분해 특성)

  • Shin, Jae-Ho;Kwak, Yun-Young;Kim, Won-Chan;So, Jai-Hyun;Shin, Hyun-Soo;Park, Jong-Woo;Kim, Tae-Hwa;Kim, Jang-Eok;Rhee, In-Koo
    • Korean Journal of Environmental Agriculture
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    • v.27 no.3
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    • pp.292-297
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    • 2008
  • A bacterium, which was named to be Bacillus sp. E64-2, capable of degrading endosulfan was isolated from the environmental sample using enrichment culture technique. The Bacillus sp. E64-2 was able to degrade 99% of 10 mg/L endosulfan in the culture media within 7 days at $30^{\circ}C$. Endosulfan diol was the only intermediate by the endosulfan degrading bacterial culture and the pH value of the culture media was significantly increased to pH 8.4 from pH 7.0 after 7 days of incubation. When the endosulfan and the crude extract of the strain were incubated, endosulfan diol was a major metabolite. Both the enzymatic reaction and the pH-increasing effect contribute to the degradation of endosulfan by the bacterial culture.

Co-Location and Analysis of an eLoran Transmitting Antenna in an MF Transmitting Site (중파방송 송신소 내 eLoran용 송신 안테나 동일 장소 배치 및 분석)

  • Kim, Ki-nam;Mok, Ha-kyun;Koo, Hanni;Nam, Sangwook
    • The Journal of Korean Institute of Electromagnetic Engineering and Science
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    • v.27 no.12
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    • pp.1053-1058
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    • 2016
  • The eLoran(enhanced Long Range Navigation) transmitting antenna is analyzed for co-location with an AM transmitting antenna in an MF transmitting site. To compensate for the loading effect, the umbrella-type loading is applied for eLoran antenna. The validity of the co-location between the MF antenna and the eLoran antenna is verified through the simulation results of the radiation pattern and the return loss. Also, coupling including antenna matching circuit is analyzed to verify the effect of the transmitting circuit. The coupling between the LF and eLoran antenna is -53.3 dB at 100 kHz and -64.8 dB at 1,053 kHz, respectively.

Elucidating Molecular Interactions of Natural Inhibitors with HPV-16 E6 Oncoprotein through Docking Analysis

  • Kumar, Satish;Jena, Lingaraja;Galande, Sneha;Daf, Sangeeta;Mohod, Kanchan;Varma, Ashok K.
    • Genomics & Informatics
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    • v.12 no.2
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    • pp.64-70
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    • 2014
  • Human papillomavirus (HPV) infection is the leading cause of cancer mortality among women worldwide. The life-threatening infection caused by HPV demands the need for designing anticancerous drugs. In the recent years, different compounds from natural origins, such as carrageenan, curcumin, epigallocatechin gallate, indole-3-carbinol, jaceosidin, and withaferin, have been used as a hopeful source of anticancer therapy. These compounds have been shown to suppress HPV infection by different researchers. In the present study, we explored these natural inhibitors against E6 oncoprotein of high-risk HPV-16, which is known to inactivate the p53 tumor suppressor protein. A robust homology model of HPV-16 E6 was built to anticipate the interaction mechanism of E6 oncoprotein with natural inhibitory molecules using a structure-based drug designing approach. Docking analysis showed the interaction of these natural compounds with the p53-binding site of E6 protein residues 113-122 (CQKPLCPEEK) and helped the restoration of p53 functioning. Docking analysis, besides helping in silico validation of natural compounds, also helps understand molecular mechanisms of protein-ligand interactions.

Packet Scheduling Algorithms for Throughput Fairness and Coverage Enhancement in TDD-OFDMA Downlink Network (TDD-OFDMA 하향 링크에서의 수율 공평성과 서비스 커버리지 보장을 위한 패킷 스케줄링 알고리즘 연구)

  • Ki, Young-Min;Kim, Dong-Ku
    • The Journal of Korean Institute of Communications and Information Sciences
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    • v.30 no.7A
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    • pp.611-619
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    • 2005
  • The present paper proposes two different packet scheduling algorithms in the IEEE 802.16e type TDD-OFDMA downlink, which are the weighted fair scheduling(WFS) and the throughput guarantee scheduling(TGS). The performance of proposed scheduling algorithms are compared to some of conventional schedulers such as round robin(RR), proportional fair(PF), fast fair throughput(FFTH), and fair throughput(FH) in terms of service coverage, effective throughput and fairness at 64 kbps and 128 kbps minimum user throughput requirements. For a relatively smaller throughput(64 kbps) requirement, the proposed algorithms provide higher improvement in the number of users per sector within 95$\%$ service coverage while satisfying the lxEV-DV fairness criterion. For a relatively larger throughput(128 kbps) requirement, the proposed algorithms provide higher coverage enhancement while maintaining the same effective aggregate throughput over PF scheduler.

Deciphering the Genes for Taste Receptors for Fructose in Drosophila

  • Uchizono, Shun;Itoh, Taichi Q.;Kim, Haein;Hamada, Naoki;Kwon, Jae Young;Tanimura, Teiichi
    • Molecules and Cells
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    • v.40 no.10
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    • pp.731-736
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    • 2017
  • Taste sensitivity to sugars plays an essential role in the initiation of feeding behavior. In Drosophila melanogaster, recent studies have identified several gustatory receptor (Gr) genes required for sensing sweet compounds. However, it is as yet undetermined how these GRs function as taste receptors tuned to a wide range of sugars. Among sugars, fructose has been suggested to be detected by a distinct receptor from other sugars. While GR43A has been reported to sense fructose in the brain, it is not expressed in labellar gustatory receptor neurons that show taste response to fructose. In contrast, the Gr64a-Gr64f gene cluster was recently shown to be associated with fructose sensitivity. Here we sought to decipher the genes required for fructose response among Gr64a-Gr64f genes. Unexpectedly, the qPCR analyses for these genes show that labellar expression levels of Gr64d and Gr64e are higher in fructose low-sensitivity flies than in high-sensitivity flies. Moreover, gustatory nerve responses to fructose in labellar sensilla are higher in Gr64d and Gr64f mutant lines than in mutant flies of the other Gr64a-Gr64f genes. These data suggest the possibility that deletion of GR64D or GR64F may indirectly induce enhanced fructose sensitivity in the labellum. Finally, we conclude that response to fructose cannot be explained by a single one of the Gr64a-Gr64f genes.