• 제목/요약/키워드: Co(II) complex

검색결과 184건 처리시간 0.022초

Decision-Makings of CoPS Innovation Strategy, Power and Dominant Design - the Case of SKT and KTF

  • Kim, Jong-Seok;Miles, Ian;Flanagan, Kieron
    • 한국기술혁신학회:학술대회논문집
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    • 한국기술혁신학회 2017년도 춘계학술대회 논문집
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    • pp.219-219
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    • 2017
  • This study aims at examining each firm's decision-makings of complex product and system (hereafter CoPS) innovation strategy, so that it tries to reveal the nature and role of CoPS innovations strategy. And it designed a comparative case study along with qualitative methods, by having two mobile operators' digital rights management (hereafter DRM) innovation in South Korea's digital music service industry. Through literature review, this study formulated three research propositions: (i) Each firm's decision-makings of CoPS innovations strategy are analytical negotiation process among economic actors in an industry; (ii) Each firm's market power originated from its market share from the installed base through network effect and switching cost influence decision-makings of CoPS innovation strategies; (iii) Each firm's decision-makings of different CoPS innovation strategies are related to their intension of achieving better market power, consequently dominant design. Through empirical examination of two mobile operators' decision-makings of DRM innovation strategy, this study empirically verified three research propositions.

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용매추출법에 의한 토양중의 미량 구리와 아연원소의 동시추출 및 정량에 관한 연구 (The Simultaneous Extraction and Determination of Trace Copper and Zinc in Solvent Extraction)

  • 정창웅;지석주;박종안
    • 한국환경보건학회지
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    • 제21권3호
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    • pp.87-95
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    • 1995
  • A rapid and selective co-extraction systems of copper and zinc-thiocyanate complex into various types of alkylamine for the simultaneous determination of two metal ions by atomic absorption spectrometry and ion chromatograph have been proposed. The quantitative extractions of Cu(II) and Zn(II) at 0.1 M-thiocyanate and 0.1 M-HCI were achieved with Aliquat 336-$CHCl_3$. The detection limits of Cu and Zn were 2 ppb and 0.9 ppb respectively.

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무창돈사의 환경제어 시스템 개발 (II) - 자돈과 육성돈의 사양성적 - (Development of Environmental Control Systems for Windowless Pig-housing (II) - Growth Performance of Weaned Piglets and Growing Pigs -)

  • 장동일;장홍희;임영일;박창식;이봉덕;이형석
    • Journal of Biosystems Engineering
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    • 제24권5호
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    • pp.425-430
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    • 1999
  • Complex environmental control systems were developed, which control properly the pig's environment in windowless pig-housing based on the thermoregulatory behaviors of pigs and concentrations of noxious gases (CO2 and NH3). The this study was conducted to assess the performance of complex environmental control systems by raising weaned piglets and growing pigs under different seasonal conditions. Average daily gain of pigs in the experimental pig-housing was slightly higher than that of pigs in the conventional pig-housing. Average daily gain was not significantly different in winter and spring(P>0.05), but was significantly different in summer(P<0.05). Feed conversion rate of pigs in the experimental pig-housing was smaller than that of pigs in the conventional pig-housing. Feed conversion rate was not significantly different in environment for weaned piglets and growing pigs resulted in the improved daily gain, feed conversion rate, and carcass quality of the finishing pigs. These results showed that the performance of the complex environmental control systems in windowless pig-housing was excellent for weaned piglets and growing pigs.

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Synthesis and Spectral Characterization of Antifungal Sensitive Schiff Base Transition Metal Complexes

  • Raman, N.;Sakthivel, A.;Rajasekaran, K.
    • Mycobiology
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    • 제35권3호
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    • pp.150-153
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    • 2007
  • New $N_2O_2$ donor type Schiff base has been designed and synthesized by condensing acetoacetanilido-4-aminoantipyrine with 2-aminobenzoic acid in ethanol. Solid metal complexes of the Schiff base with Cu(II), Ni(II), Co(II), Mn(II), Zn(II), VO(IV), Hg(II) and Cd(II) metal ions were synthesized and characterized by elemental analyses, magnetic susceptibility, molar conduction, fast atom bombardment (FAB) mass, IR, UV-Vis, and $^1H$ NMR spectral studies. The data show that the complexes have the composition of ML type. The UV-Vis. and magnetic susceptibility data of the complexes suggest a square-planar geometry around the central metal ion except VO(IV) complex which has square-pyramidal geometry. The in vitro antifungal activities of the compounds were tested against fungi such as Aspergillus niger, Aspergillus flavus, Rhizopus stolonifer, Candida albicans, Rhizoctonia bataicola and Trichoderma harizanum. All the metal complexes showed stronger antifungal activities than the free ligand. The minimum inhibitory concentrations (MIC) of the metal complexes were found in the range of $10{\sim}31{\mu}g/ml$.

부분적으로 Co(Ⅱ) 이온으로 치환한 제올라이트 A를 탈수한 후 메탄올을 흡착한 결정구조 (Crystal Structure of a Methanol Sorption Complex of Dehydrated Partially Cobalt(Ⅱ)-Exchanged Zeolite A)

  • 장세복;한영욱;김양
    • 대한화학회지
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    • 제38권5호
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    • pp.339-344
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    • 1994
  • 부분적으로 $Co^{2+}$이온으로 치환한 제올라이트 A를 탈수한 후 메탄올을 흡착한 결정구조 즉 $Co_4Na_4Si_{12}Al_{12}O_{48}{\cdot}$6.5CH_3OH$ (a = 12.169(1) $\AA)$를 입방공간군 Pm$\bar3$m를 사용하여 단결정 X-선 회절법으로 해석하고 정밀화하였다. $Co_4Na_4$-A 제올라이트를 $360^{\circ}C$ 에서 $2{\times}10^{-6}$ torr하에서 2일간 진공탈수한 후 $22(1)^{\circ}C$에서 약 104 torr의 메탄올 증기로 약 1시간 동안 흡착시켜 결정을 만들었다. Full matrix최소자승법 정밀화 계산에서 I > $3\sigma(I)$인 147개의 독립반사를 사용하여 최종오차인자를 $R_1$ = 0.061, $R_2$ = 0.060까지 정밀화시켰다. 단위세포당 4개의 $Co^{2+}$ 이온과 1.5개의 $Na^+$ 이온은 6-링 산소와 결합하고 있었다. 4개의 $Co^{2+}$ 이온은 O(3)의 (111)평면에서 큰 동공쪽으로 약 0.44 $\AA$ 들어가 위치하고 1.5개의 $Na^+$ 이온은 O(3)의 (111)평면에서 소다라이트 동공 깊숙히 약 0.55 $\AA$ 들어간 자리에 위치하고 있다. 2.5개의 $Na^+$ 이온은 8-링 평면상에 위치한다. 단위세포당 약 6.5개의 메탄올 분자가 흡착되었다. 이들 메탄올 분자는 큰 동공내에 위치하고 있고, 4개의 $Co^{2+}$이온과 2.5개의 $Na^+$이온과 결합하고 있다. 4개의 메탄올의 산소는 6-링에 위치한 $Co^{2+}$이온과 결합하고 나머지 2.5개의 메탄올의 산소는 8-링에 위치한 $Na^+$이온과 결합하고 있다.

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한국형발사체 추진제공급시스템 충전모드 해석 (Analysis on the Filling Mode of Propellant Supply System for the Korea Space Launch Vehicle)

  • 이재준;박상민;강선일;오화영;정은상
    • 한국추진공학회지
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    • 제20권4호
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    • pp.50-58
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    • 2016
  • 한국형 발사체(KSLV-II) 추진제 공급시스템은 각 단에 위치한 추진제 탱크에 산화제와 케로신을 공급해주는 시스템이다. 발사체의 추진제 탱크를 안정적으로 충전하기 위해, 충전시나리오와 충전유량을 결정하였다. 다음으로 1D 유동 해석프로그램을 이용하여 추진제 공급시스템을 모델링 하였다. 1D steady state 해석을 통하여 각 시스템에서의 충전모드에 따른 밸브용량과 orifice 사이즈를 계산하였다. Steady state 결과를 이용하여 1D transient 해석을 수행하였다. 해석 결과 추진제가 각 추진제 탱크로 충전됨에 따라 탱크의 수두가 상승하여 충전유량이 감소하는 것으로 나타났다. 최종적으로 해석을 통해 제안된 충전시스템 모델이 요구되는 충전설계조건을 만족하는 것을 확인하였다.

질소-산소 주개 거대고리 화합물-금속착물의 수용액에서의 안정도상수 (Stability Constants of Nitrogen-Oxygen Donor Macrocyclic Ligand-Metal Ion Complexes in Aqueous Solutions)

  • 김정;윤창주;박휴범;김시중
    • 대한화학회지
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    • 제35권2호
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    • pp.119-127
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    • 1991
  • 고리를 구성하는 원자의 수가 15개에서 18개인 디아자 크라운계의 고대고리 화합물인 1,12-diaza-3, 4 : 9, 10-dibenzo-5, 8-dioxacyclopentadecane(NtnOenH$_4$), 1,13-diaza-3,4 : 10,11-dibenzo-hydroxy-5,9-dioxacyclohexadecane(NtnOtnH$_4$), 1,13-diaza-3,4 : 10,11-dibenzo-15-hydroxy-5,9-dioxacyclohexadecane(Ntn(OH)OtnH$_4$), 1,15-diaza-3,4 : 12,13-dibenzo-5,8,11-trioxacycloheptadecane (NenOdienH$_4$) and 1,15-diaza-3,4 : 12,13-dibenzo-5,8,11-trioxacyclooctadecane(NtnOdienH$_4$)의 양성자화와 금속이온과의 착물 형성을 전위차적정법과 핵자기 공명법으로 연구하였다. 양성자화상수는 크라운 에테르의 염기도를 예측하는데 상용하였다. 본 연구에서 사용한 거대고리 화합물의 염기도 순서는 NenOdienH$_4$ < Ntn(OH)OtnH$_4$ < NtnOenH$_4$ < NtnOtnH$_4$ < NtnOdienH$_4$였다. 염기도의 이와 같은 변화를 거대고리에 대한 치환기와 양성자화가 일어날 때의 고리의 비틀림 정도로 설명하였다. 금속이온과의 착물 형성에 대한 안전도상수는 전이금속이온에 대해서는 Co(II) < Ni(II) < Cu(II) < Zn(II)순이었으며, 중금속이온에 대해서는 Cd(II) < pb(II) < Hg(II)의 순이었다. 금속 착물 형성에 대한 이와 같은 안정도상수의 변화에는 Co(II), Ni(II) 및 Cu(II) 착물의 경우 리간드 고리의 크기가 영향을 미치고 있었으며, Zn(II), Cd(II), pb(II) 및 Hg(II) 착물의 경우에는 리간드의 염기도가 주로 영향을 미치고 있었다. 후전이금속 착물에 대한 $^1$H와 $^{13}$C 핵자기공명 분광법에서는 고리의 질소원자가 산소원자보다 금속이온에 더 큰 친화력을 가짐을 알 수 있었고, 금속이온과 착물을 형성할 때에 고리의 평면성이 상실되고 있음도 밝혀졌다.

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Sorption of Thiocyanate Silver Complexes and Determination of Silver by Diffuse Reflectance Spectroscopy

  • Kononova, O.N.;Goryaeva, N.G.;Vorontsova, T.V.;Bulavskaya, T.A.;Kachin, S.V.;Kholmogorov, A.G.
    • Bulletin of the Korean Chemical Society
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    • 제27권11호
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    • pp.1832-1838
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    • 2006
  • The present paper is focused on sorption concentration of silver (I) on some complex-forming ion exchangers in the initial thiocyanate form and subsequent determination of Ag(I) in the phase of anion exchanger AN-25 by diffuse reflectance spectroscopy. The sorption and kinetic characteristics of the sorbents were investigated. The apparent stability constants of thiocyanate silver complexes in the ion exchanger phase were calculated. The sorption-spectroscopic method is proposed for Ag(I) determination in aqueous solutions. The calibration curve is linear in the concentration range of 10-200 mg/L (sample volume is 10.0 mL) and the detection limit is 2 $\mu$g/mL. The presence of $Na^+,\;K^+,\;Mg^{2+}$ (macrocomponents) as well as of Ni (II), Co (II), Cu (II) do not hinder the determination of silver (I).

Cloning, Sequencing, and Characterization of the Pradimicin Biosynthetic Gene Cluster of Actinomadura hibisca P157-2

  • Kim, Byung-Chul;Lee, Jung-Min;Ahn, Jong-Seog;Kim, Beom-Seok
    • Journal of Microbiology and Biotechnology
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    • 제17권5호
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    • pp.830-839
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    • 2007
  • Pradimicins are potent antifungal antibiotics having an unusual dihydrobenzo[$\alpha$]naphthacenequinone aglycone substituted with D-alanine and sugars. Pradimicins are polyketide antibiotics produced by Actinomadura hibisca P157-2. The gene cluster involved in the biosynthesis of pradimicins was cloned and sequenced. The pradimicin gene cluster was localized to a 39-kb DNA segment and its involvement in the biosynthesis of pradimicin was proven by gene inactivation of prmA and prmB(ketosynthases $\alpha\;and\;\beta$). The pradimicin gene cluster consists of 28 open reading frames(ORFs), encoding a type II polyketide synthase(PKS), the enzymes involved in sugar biosynthesis and tailoring enzymes as well as two resistance proteins. The deduced proteins showed strong similarities to the previously validated gene clusters of angucyclic polyketides such as rubromycin, griseorhodin, and fredericamycin. From the pradimicin gene cluster, prmP3 encoding a component of the acetyl-CoA carboxylase complex was disrupted. The production levels of pradimicins of the resulting mutants decreased to 62% of the level produced by the wild-type strain, which indicate that the acetyl-CoA carboxylase gene would have a significant role in the production of pradimicins through supplying the extender unit precursor, malonyl-CoA.

Hydrogenation of trans-Cinnamaldehyde with Hydrido-Carbonyl Osmium(II) Complexes of Chelating Phosphine Ligands

  • 정민교;허성;이원용;전무진
    • Bulletin of the Korean Chemical Society
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    • 제18권8호
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    • pp.806-810
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    • 1997
  • A series of new hydridocarbonyl osmium(Ⅱ) complexes, OsHCl(CO)(PPh3)(L-L)[L-L=Ph2P(CH2)nPPh2 (n=1 (1), 2 (2), 3 (3), cis-Ph2PCH=CHPPh2 (4), and Fe(η5-C5H4PPh2)2 (5)] has been synthesized from OsHCl(CO)(PPh3)3 and chelating diphosphines. These complexes have been characterized by IR, 1H NMR and elemental analysis. The catalytic activities of these complexes both for the transfer hydrogenation of trans-cinnamaldehyde with 2-propanol as the hydrogen donor, and for the selective hydrogenation of trans-cinnamaldehyde with H2, have been examined. Complexes (1)-(5) were shown to have higher selectivities for the transfer hydrogenation of the C=O bond of aldehyde than for the transfer hydrogenation of the C=C bond of aldehyde. The selectivities for the transfer hydrogenation with 2-propanol as well as for the hydrogenation with H2 have been found to decrease in the order 3 > 5 > 2 > 4 > 1. Complex (3) has shown to possess almost 90% of the selectivity to cinnamyl alcohol for transfer hydrogenation. It is also found that there is a correlation between the ν(CO) of each complex and the hydrogenation, of the C=O bond of trans-cinnamaldehyde. Overall, the selectivities with the complexes (1)-(5) are greater for the transfer hydrogenation with 2-propanol than for the hydrogenation with H2.