• Title/Summary/Keyword: [ph]

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The Optimal Spare Level of a Weapon System having Phase-type Repair Time (Phase-type 수리시간을 갖는 무기체계의 적정예비품수 결정)

  • Yoon, Hyouk;Lee, Sang-Jin
    • Korean Management Science Review
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    • v.26 no.3
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    • pp.145-156
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    • 2009
  • The probability distribution of the repair process should be determined to choose the optimal spare level of a weapon system with a queueing model. Though most weapon systems have a multi-step repair process, previous studies use the exponential distribution for the multi-step repair process. But the PH distribution is more appropriate for this case. We utilize the PH distribution on a queueing model and solve it with MGM(Matrix Geometric Method). We derive the optimal spare level using the PH distribution and show the difference of results between the PH and exponential distribution.

Cloning and Sequencing of the rph Gene Encoding RNase PH from Legionella pneumophila

  • Kim, Se-Jin;Lim, Jong-Seok;Cianciotto, Nicholas P.;Choe, Yong-Kyung
    • Journal of Microbiology
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    • v.37 no.4
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    • pp.218-223
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    • 1999
  • Legionella pneumophila, the cause of Legionnaires disease, is able to survive intracellularly in eukaryotic cells such as monocytes, macrophages, and protozoan organisms. During protein biosynthesis, the rph gene encodes ribonuclease (RNase) PH which functions as a phosphorolytic nuclease that removes nucleotides following the CCA terminus of tRNA and as a nucleotidyl-transferase which adds nucleotides to the ends of RNA molecules by usingnucelside diohosphates as substrates. In this sutdy, the rph gene was screened in pUC19 library employing a DNA probe which was constructed from PCR based on a consensus pattern of multiple alignment of RNas PH. The encoded protein consists of 235 amino acid residues with a calculated molecular weight of 26,112 Daltons. The RNase PH signature domains are completely conserved.

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The Effects of Baldness on the Compression-Rebounding Properties of Shoe Midsole (발포체의 경도가 신발 중창의 압축-반발 특성에 미치는 영향)

  • Park, Cho-Cheol
    • Elastomers and Composites
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    • v.39 no.3
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    • pp.186-192
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    • 2004
  • Compression and rebounding properties of IP(injection phylon), PH(phylon) and PU(polyurethane) foams were studied. The compression stress, rebounding stress, loss compression energy and storage compression energy of foams were decreased with increasing hardness of foams. The compression stress, loss compression energy of IP foams were lower than those of PH and PU. Rebounding stress and storage compression energy of PU foams were higher than those of IP and PH. The compression stress and rebounding of PH foam were lower than those of IP and PU.

C1 HERMITE INTERPOLATION WITH MPH CURVES USING PH-MPH TRANSITIVE MAPPINGS

  • Kim, Gwangil;Kong, Jae Hoon;Lee, Hyun Chol
    • Journal of the Korean Mathematical Society
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    • v.56 no.3
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    • pp.805-823
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    • 2019
  • We introduce polynomial PH-MPH transitive mappings which transform planar PH curves to MPH curves in ${\mathbb{R}}^{2,1}$, and prove that parameterizations of Enneper surfaces of the 1st and the 2nd kind and conjugates of Enneper surfaces of the 2nd kind are PH-MPH transitive. We show how to solve $C^1$ Hermite interpolation problems in ${\mathbb{R}}^{2,1}$, for an admissible $C^1$ Hermite data-set, by using the parametrization of Enneper surfaces of the 1st kind. We also show that we can obtain interpolants for at least some inadmissible data-sets by using MPH biarcs on Enneper surfaces of the 1st kind.

Homogeneous Catalysis (IV). Hydrogenation of Acrylonitrile with trans-Chlorocarbonylbis(triphenylphosphine)rhodium(I)

  • Woo, Jin-Chun;Chin, Chong-Shik
    • Bulletin of the Korean Chemical Society
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    • v.4 no.4
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    • pp.169-171
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    • 1983
  • It has been found that the acrylonitrile solution of trans-$RhCl(CO)(Ph_3P)_2$ produces propionitrile catalytically at $90^{\circ}C$ under $P_{H_2}$=3 atm. This catalytic hydrogenation proceeds only for a certain period of time producing ca. 50 moles of propionitrile per mole of the rhodium complex. The hydrogenation with trans-$RhCl(CO)(Ph_3P)_2$ in the presence of formaldehyde is much faster than in the absence of formaldehyde, and continues without a decrease in the rate for a prolonged period of time. It is suggested that the hydrogenation with trans-$RhCl(CO)(Ph_3P)_2$ proceeds through the unsaturated route initiated by the dissociation of CO from trans- $RhCl(CO)(Ph_3P)_2$ to give coordinatively unsaturated $RhCl(Ph_3P)_2$.

Study on the Protein Binding of Anti-cancer Agent, 2"-O-benzoylcinnamaldehyde, using Ultrafilteration and Flurescence Spectrometry

  • Ren , Shan;Kim, Dae-Duk;Lee, Chi-Ho
    • Proceedings of the PSK Conference
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    • 2003.10b
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    • pp.242.3-243
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    • 2003
  • The compound of 2"-O-benzoylcinnamaldehyde(CB-ph) is a derivative of 2"-hydroxycinnamaldehyde whcih is a methanol extract of cinnamomum cassia blume. It"s a new anti-cancer agent which has been showed to inhibit the growth of various tumor cells in vitro and in vivo. In order to investigate the effective drug concentration and bio-distribution of CB-ph, the plasma protein binding was studied. In this study, the degree of the binding of Cb-ph to various serum proteins, the binding parameters, the binding site of CB-ph in human serum albumin, and the effect of some extensive protein-binding drugs on the protein binding of CB-ph in human serum ablumin were investigated respectively by ultrafilteration and fluorescence spectrometry. (omitted)

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Oxidation of trans-[FeH(NCS(Me)-S)(dppe)2]I to trans trans-[FeNCS)2(Ph2P(O)CH2CH2P(O)Ph2)2][I3](dppe=PPh2CH2CH2PPh2) (trans-[FeH(NCS(Me)-S)(dppe)2]I 화합물의 trans-[FeNCS)2(Ph2P(O)CH2CH2P(O)Ph2)2][I3]로 산화)

  • Lee, Ji Hwa;Lee, Soon W.
    • Journal of the Korean Chemical Society
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    • v.44 no.4
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    • pp.311-315
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    • 2000
  • The Fe(II)-isothiocyanato complex $trans-[FeH(NCS)(dppe)_2]$ (1) eactedwith iodomethane(Mel) to give methyl isothiocyanide-Fe(n) complex, $trans-FeH(NCS(Me)-S)(dppe)_2]I(2)$. Compound 2 was oxidized to $trans-[Fe(NCS)_2(Ph_2P(O)CH_2CH_2P(O)Ph_2)_2][I_3]$ (3), which was structurally characterized by X-ray diffraction. The molecular structure of 3 showed a bent Fe-NCS group, Crystallographic data for 3: triclinic space group P1,a=11.071(2) A,b=12.054(2)A,c=12.121(1)A, $\alpha=101.02(1){\circ}C{\beta}=95.887(9){\circ}Cr=110.34(1){\circ}C$, $Z=1R(wR_2)=0.0567(0.1294)$.

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Natrate reductase activity of 4 mosses including ctenidium molluscum in relation to increasing acidic deposition from atmosphere (大氣中의 酸性降下物의 增加에 따른 Ctenidium molluscum 등 4 종 蘇類의 窒酸還元酵素 活性)

  • Ihm, Byung-Sun;Lee, Jeom-Sook
    • The Korean Journal of Ecology
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    • v.15 no.4
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    • pp.355-363
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    • 1992
  • Nitrate reductase activity(NRA) and induced NRA were compared in 4 species of moss ctenidium molluscum, homalothecium, tortella tortusa and neckera crispa collected from limestone in england. the NRA and dry weight of the c. molluscum were also measured after spraying with acidic deposition adjusted to ph 5.6, 4.6, 3.6 and 2.8 with one of two molar ratios of nitric to sulfuric acid, i.e. 1:0(N alone) and 1:2(1N+2S) for 20 days. All 4 species showed high NR leavels in the upper part of cut shoots and occurred maximum inducation of NRA within 6h. c. molluscum had the highest NRA levels among 4 species. after daily spraying of acidic deposition, NRA of c. molluscum was increased much more largely at ph 6 and ph 3.6 derived from N alone than from 1N+2S. However that was decreased at ph 2.8 derived both from N alone and 1N+2S . Decline of dry weight had occurred at ph 3.6 and 2.8 derived both from N alone and 1N+2S. Whereas substantial fertilization effect was observed at ph 4.6 derived from N alone. the data suggest that c. molluscum are able to utilize nitrate more effectivery than any other species, and NRA induction are more sensitive than growth response to nitrogen content of acidicdeposition in a short- term. however toxic effects was detected at high $NO_3$ supply and low phacidic deposition.

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Electrical Conduction and Emission Properties of (tb-PMP)3Tb-(Ph3PO) Single Layer OLEDs ((tb-PMP)3Tb-(Ph3PO) 단일층 OLEDs의 전기전도 및 발광 특성)

  • Moon, Dae-Gyu
    • Journal of the Korean Institute of Electrical and Electronic Material Engineers
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    • v.19 no.9
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    • pp.878-882
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    • 2006
  • We have fabricated single organic layer devices of the organolanthanide complex, terbium tris-(1-phenyl-3-methyl-4-(tertiarybutyry)pyrazol-5-one)triphenylphosphine oxide [$(tb-PMP)_{3}Tb-(Ph_{3}PO)$] for the investigation of its light emission and electrical conduction properties. The thickness of ($(tb-PMP)_{3}Tb-(Ph_{3}PO)$) layer was varied to 60, 75, 95 nm. Mg and Ca layers were used for the cathode contact. The electrical conduction in the $(tb-PMP)_{3}Tb-(Ph_{3}PO)$ single layer devices was dominated by the injection of electrons into the organic layer from the cathode. A higher current density at much lower voltages can be attained with Ca cathode because of the enhanced electron injection. The device shows very sharp emission at 548 nm. The FWHM of the strongest emission peak was 12 nm.

THERMAL POLYMERIZATION OF 2-HYDROXYETHYL METHACRYLATE WITH PHENYLSILANS (PHENYLSILANS와 2-HYDROXYETHYL METHACRYLATE의 열중합)

  • Sung, A Young
    • Journal of Korean Ophthalmic Optics Society
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    • v.5 no.2
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    • pp.87-90
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    • 2000
  • Poly(HEMA)s have been used as the optometric material for the preparation of soft contact lens. The bulk thermal polymerization of 2-hydroxyethyl methacrylate (HEMA) with various hydrosilanes such as $phSiH_3$, $phMeSiH_2$, and $ph2SiH_2$ were performed to produce poly(HEMA)s containing phenylsilyl end moeity. It was found for thermal polymerization that while the polymerization yield and polymer molcular weights decreased as the relative phenylsilane concentration increases, the TGA residue yields and the relative intensities of SiH IR stretching bands increased as the relative hydrosilane concentration increases over HEMA. The polymerization yield, molecular weight, and TGA residue for the thermal polymerization were higher than those for the photo polymerization. Thus, the hydrosilanes significantly influence on the polymerization as both chain-initiation and chain-transfer agents.

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