• 제목/요약/키워드: C1-2 fusion

검색결과 544건 처리시간 0.035초

LTCC용 Mg-Si-O계 글라스-세라믹스의 유전특성 (Dielectric Properties of Mg-Si-O system glass-ceramics for LTCC applications)

  • 조정환;여동훈;신효순;홍연우;김종희;남산
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2007년도 추계학술대회 논문집
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    • pp.274-274
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    • 2007
  • LTCC 소재로 응용을 위해 Mg-Si-O계 세라믹스에 glass frit을 첨가하여 소결 및 마이크로파 유전특성에 관한 연구를 진행하였다. $Mg_2SiO_4$를 기본조성으로 하고 $B_2O_3-ZnO-Na_2O-SiO_2-Al_2O_3$계 glass를 20~40wt%로 첨가하여 $900^{\circ}C$에서 1시간 소결하였을 때 glass 함량이 증가함에 따라 밀도$(g/cm^3)$ 및 유전율$(\varepsilon_r)$은 증가하였고 품질계수$(Q{\times}f_0)$ 값은 감소하는 경향을 보였다. $900^{\circ}C$에서 1시간 소결한 소결체의 유전특성은 유전율 $(\varepsilon_r)$ = 6.5, 품질계수 $(Q{\times}f_0)$ = 4,000(GHz), 온도계수 $({\tau}_f)={\pm}10ppm/^{\circ}C$로 우수한 특성을 확인하였다. 그리고 Glass Milling 효과에 따른 glass-ceramics 소결체의 미세구조, 마이크로파 유전특성을 비교 고찰하였다.

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Constitutive Expression of Lipase on the Cell Surface of Escherichia coli using OmpC Anchoring Motif

  • Lee, Seung Hwan;Lee, Sang Yup
    • Korean Chemical Engineering Research
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    • 제58권2호
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    • pp.280-285
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    • 2020
  • We have developed a constitutive display system of the Pseudomonas fluorescens SIK W1 TliA lipase on the cell surface of Escherichia coli using E. coli outer membrane protein C (OmpC) as an anchoring motif, which is an economical compared to induced system. For the constitutive expression of truncated OmpC-TliA fusion proteins, gntT104 promoter was employed. Cell growth was not affected by over expression of fusion protein during entire culture time, suggesting cell lysis was not a problem. The localization of truncated OmpC-TliA fusion protein on the cell surface was confirmed by immunofluorescence microscopy and measuring whole cell lipase activity. Constitutively displayed lipase was very stable, retaining activity enantioselectivity throughout the five repeated reactions. These results suggest that OmpC from E. coli be a useful anchoring motif for displaying enzymes on the cell surface without any inducers, and this stable surface display system can be employed for a broad range of biotechnological applications.

Cellulase를 생산하는 Aspergillus niger MAN-831과 Aspergillus wentii MAW-538의 원형질체 형성 및 융합 (Formation and Fusion of Protoplasts from the Cellulolytic Fungi, Aspergillus niger MAN-831 and Aspergillus wentii MAW-538)

  • 박석규;이상원;문일식;손봉수;강성구
    • 한국식품영양과학회지
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    • 제24권6호
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    • pp.964-969
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    • 1995
  • 섬유성 biomass의 효율적인 이용을 위하여 CMCase, avicelase 분비력이 높은 균주(A. wentii MAW-598)와 ${\beta}-glucosidase$ (A. niger MAN-831) 분비력이 우수한 균주의 포자를 이용한 원형질세 형성.재생조건 및 융합을 실시하였다. 원형질체 형성 및 재생의 최적조건은 5일 성숙한 포자를 $30\mu\textrm{g}/ml$ 농도의 2-DG로 4시간 전배양하여 0.7M KCI 삼투압 안정제, novozyme(7.5mg/ml)+driselase(2.5mg/ml) 혼합효소로 5시간 반응시키는 것이 효과적이었다. 원형질체 융합 조건은 $CaCl_2$ 15mM, 25% PEG 4000, pH 5-7, $36^{\circ}C$에서 25~30분간 처리하였을때 효과적이었으며, 융합빈도는 $7.94\;{\times}\;10^{-4}$로 나타났다. FA-208 융합주는 친주에 비하여 각각 1.5, 1.3, 1.2배 효소활성의 증가를 나타내었다.

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알칼리 용융 및 수열 합성에 의한 석탄회로부터 제올라이트 A의 합성 (Synthesis of zeolite A from coal fly ash by alkali fusion followed by hydrothermal treatment)

  • 정지백;최고열
    • 한국응용과학기술학회지
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    • 제32권2호
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    • pp.240-247
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    • 2015
  • 석탄회를 NaOH로 용융시킨 후 수열 처리에 의하여 제올라이트 A를 합성하였다. NaOH/석탄회의 비, 용융 온도, $NaAlO_2$의 첨가량, 수열 처리 온도 및 시간이 생성된 제올라이트의 종류와 결정도에 미치는 영향에 대하여 연구하였다. 결정도가 높은 제올라이트의 생성에 필요한 최적의 NaOH/석탄회의 중량비는 1.2, 최적의 용융 온도는 $550^{\circ}C$이었다. 용융된 석탄회로부터 $Si^{4+}$$Al^{3+}$의 용출은 교반 시간의 영향을 받지 않았다. 생성된 제올라이트의 형태는 첨가한 $NaAlO_2$의 영향을 받는 것으로 나타났다. 적은 양의 $NaAlO_2$를 첨가하면 제올라이트 X가 생성되나 $NaAlO_2$의 양이 증가하면 단일상의 제올라이트 A가 생성되었다. 수열처리 시간과 온도가 증가하면 제올라이트 A는 hydroxysodalite로 변화 하였다. 승온 속도를 낮춰 반응 온도까지의 도달시간을 증가시키면 결정도가 좋은 제올라이트 A를 얻을 수 있었다.

핵융합로 블랭킷용 저방사화 철강재료 TIG 용접부의 강도특성 (Strength Characteristics of Reduced Activation Ferritic Steel for Fusion Blanket by TIG Welding)

  • 윤한기;이상필;김동현
    • Journal of Welding and Joining
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    • 제21권1호
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    • pp.87-92
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    • 2003
  • JLF-1 steel (Fe-9Cr-2W-V-Ta), reduced activation ferritic steel, is one of the promising candidate materials for fusion reactor applications. Tensile properties of JLF-1 base metal and its TIG weldments has been investigated at the room temperature, $400^{\circ}C$ and $600^{\circ}C$. The tensile strength of base metal (JLF-1) showed the level between those of weld metal and the Heat Affected Zone (HAZ). When the test temperature was increased from room temperature to high temperature ($400^{\circ}C$ and $600^{\circ}C$), both strength and ductility decreased or base metal, weld metal and the HAZ. The longitudinal specimens of base metal represented similar strength and ductility at room temperature and high temperature, compared to those of transverse specimens. Little anisotropy for the rolling direction was observed in the base metal of JLF-1 steel.

용액 결정성장하의 Nylon 4,6 의 결정구조 및 열적성질 (Crystal structure and thermal properties of solution crystallized nylon 4,6)

  • 김연철;홍성권
    • 한국재료학회:학술대회논문집
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    • 한국재료학회 1993년도 춘계학술발표회
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    • pp.99-100
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    • 1993
  • Calorimetric (D.S.C) studies were carried out on the nylon 4,6 single crystals grown from 1,4-butanediol solution at various crystallisation temperatures, based on the assessment of the lamellar thickness by small angle x-ray scattering. Samples were annealed mainly ot get rid of residual solvents inside the crystals. The effect of annealing on the crystal perfection is inferred from the measured thermal properties of the crystals. Accordig to the scanning rates less than 80 K/min., D. S C. melting peaks indicate that changes in the internal morphology of nylon 4,6 crystals preapred at different crystallisation temeratures yield a thermodynamic melting temperature. Tm, of 319 $^{\circ}C$, for the infinitely extended crystal thickness (1/ι). The obtained heat of fusion value for the inginite crystal thickness, Ho, was 270 J/g from the plot of measured feat of fusion ($\Delta$Hm) vs. reciprocal crystal thickness (1/ι). based on these values, the fold surface energy, $\delta$e. of 65.4 erg/$\textrm{cm}^2$ was obtained from Hoffman-Waeeks equation. The thermodynamic melting temperature and heat of fusion of the infinite crystal thickness for the solution grow nylon 4,6 single crystals are found to be higher than of the reported corresponding solution grown nylon 6,6 single crystals. pbtained crystallinity from D. S. C measurements ranges from 40 to 50 %, which is close to the reported yalue for the nylon 6,6 single ctystals but lower than we expected.

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전기자극법에 의한 생쥐 2세포기란의 분할구 융합에 관한 연구 (Blastomeres Fusion of 2-cell Mouse Embryos by Electric Stimulation)

  • 양부근;한상익;김정익
    • Clinical and Experimental Reproductive Medicine
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    • 제18권1호
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    • pp.35-40
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    • 1991
  • To find out the suitable method for blastomeres fusion of mouse 2-cell embryo using electric stimuli, these studies were carried out with various voltages (1.0 KV, 1.2 KV, 1.5 KV, 1.7 KV and 2.0KV), pulse duration times($50{\mu}\;sec$, $75/{\mu}\;sec$, $100{\mu}\;sec$) and different fusion solutions. In addition, the fused embryos were cultured for 72-80hr to observe their subsequent development. These results were summarized as follows: 1. The proportion of the fused embryos were 50.8%(34/67), 60.7%(34/56), 70.6%(48/68), 66.7% (48/72) and 85.3% (58/68) after stimuli of 1.0KV, 1.2KV, 1.5KV, 1.7KV and 2.0KV for $100{\mu}\;sec$ with 2 times, and the electric stimulation at 2.0KV(85.3%) was the most effective voltage on the blastomere fusion. 2. For in vitro development, blastocysts of the fused embryos were cultured for 72-80hrs in $M_{16}$ medium. The group(52.1%) treated with 1.5KV for $100{\mu}\;sec$ with 2 times showd higher development rates than those any other group. However, these results were not corresponded to those of the rates of blastomere fusion. 3. There were no significant differences among the rates of blastomeres fusion to 50(70.6%), 75(71.9%), and 100(78.0%) ${\mu}sec$ stimulation at 1.5KV with two times. However, the development rates of the fused embryo in vitro were 52.1%(25/48), 28.3%(13/46) and 9.4%(3/32) at the above conditions, and the development rates of fused embryo increased as the pulse duration times increased. 4. The rates of the blastomeres fusion were 38.9% (28/72) or 70.6% (48/68) in electrolyte (PBS) or non-electrolyte(0.3M mannitol) solution. The development rates of the fused embryo were 32.1% (9/28) or 52.1%(25/48) in the above fusion solutions, and non-electrolyte-treated group showed higher development rates of embryo than that of electrolyte-treated group.

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핵융합로용 저방사화 철강재료(RAFs)의 크리프 특성평가 (Evaluation on Creep properties of Reduced Activation Ferritic Steel(RAFs) for Nuclear Fusion Reactor)

  • 공유식;윤한기;김동현;박이현;남승훈
    • 한국해양공학회:학술대회논문집
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    • 한국해양공학회 2003년도 추계학술대회 논문집
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    • pp.146-151
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    • 2003
  • Reduced Activation Ferritic/Martenstic (RAFs) are leading candidates for structural materials of D-T fusion reactor. One of The RAFs, JLF-1 (9Cr-2W-V, Ta) has been developed and proved to have good resistance against high-fluency neutrino irradiation and good phase stability. Recently, in order to clarify the strengthening mechanical at high temperature, a new scheme to improve high temperature mechanical properties is desired. Therefore, the creep properties and creep life prediction by Larson-Miller Parameter method for JLF-1 to be used for fusion reactor materials or other high temperature components were presented at the elevated temperatures of $500^{\circ}C$, $550^{\circ}C$, $600^{\circ}C$, $650^{\circ}C$ and $704^{\circ}C$. It was confirmed experimentally and quantitatively that a creep life predictive e벼ation at such various high temperatures was well derived by LMP.

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Expression and Characterization of Uropathogenic Escherichia coli Adhesin Protein Linked to Cholera Toxin A2B Subunits in Escherichia coli TB1

  • Lee, Yong-Hwa;Ryu, Dong-Kyun;Kim, Byung-Oh;Pyo, Suhk-Neung
    • Journal of Microbiology and Biotechnology
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    • 제13권4호
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    • pp.552-559
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    • 2003
  • The FimH subunit of type 1-fimbriated Escherichiu coli (E. coli) has been determined as a major cause for urinary tract infections. Thus, to produce a possible vaccine antigen against urinary tract infections, the fimIH gene was genetically coupled to the ctxa2b gene and cloned into a pMAL-p2E expression vector. The chimeric construction of pMALfimH/ctxa2b was then transformed into E. coli K-12 TB1 and its nucleotide sequence was verified. A fusion protein, based on fusing adhesin to the cholera toxin subunit A2B (CTXA2B), was induced with 0.01 mM isopropyl-${\beta}-D-thiogalactoside$ (IPTG) for 4 h at $37^{\circ}C$ to yield a soluble fusion protein. The fusion protein was then purified by affinity chromatography. The expressed fusion protein was confirmed by SDS-PAGE and Western blotting using antibodies to the maltose binding protein (MBP) or the cholera toxin subunit B (CTXB), plus the N-terminal amino acid sequence was also analyzed. The orderly-assembled fusion protein was confirmed by a modified $G_{Ml}-ganglioside$ ELISA, using antibodies to adhesin. The results indicated that the purified fusion protein was an adhesin/CTXA2B protein containing E. coli adhesin and the $G_{Ml}-ganglioside$ binding activity of CTXB. Accordingly, this adhesin/CTXA2B protein may be a potential antigen for oral immunization against uropathogenic E. coli.

Increase in the Contents of Ginsenosides in Raw Ginseng Roots in Response to Exposure to 450 and 470 nm Light from Light-Emitting Diodes

  • Park, Sang-Un;Ahn, Deok-Jong;Jeon, Hyeon-Jeong;Kwon, Tae-Ryong;Lim, Hyoun-Sub;Choi, Bo-Seong;Baek, Kwang-Hyun;Bae, Han-Hong
    • Journal of Ginseng Research
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    • 제36권2호
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    • pp.198-204
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    • 2012
  • An light-emitting diode (LED)-based light source was used as a monochromatic light source to determine the responses of raw ginseng roots (Panax ginseng Meyer) to specific emission spectra with respect to the production of ginsenosides. The ginsenoside content in the ginseng roots changed in response to the LED light treatments at $25^{\circ}C$ relative to the levels in the control roots that were treated in the dark or at $4^{\circ}C$ for 7 d. Ginseng roots were exposed to LEDs with four different peak emission wavelengths, 380, 450, 470, and 660 nm, in closed compartments. Compared with the control $4^{\circ}C$-treated roots, roots that were treated with 450 and 470 nm light showed a significantly increased production of ginsenosides (p<0.05), with increases of 64.9% and 74.1%, respectively. The contents of the ginsenosides $Rb_2$, Rc, and $Rg_1$ were significantly higher (p<0.05) in the 450 and 470 nm-treated root samples. The ratio of protopanaxadiol ginsenosides ($Rb_1$, $Rb_2$, Rc, and Rd) to protopanaxatriol ginsenosides ($Rb_1$, $Rb_2$, Re, and Rf) was significantly higher (p<0.05) in the 450 and 470 nm-treated root samples than in the control $4^{\circ}C$-treated roots. This is the first report that demonstrates the increase and conversion of ginsenosides in raw ginseng roots in response to exposure to LED light.