• 제목/요약/키워드: 2-butanol solution

검색결과 63건 처리시간 0.185초

시금치(Spinacia oleracea L.) 엽록체의 광합성 전자전달 활성에 미치는 iso-Butanol의 영향 (Effects of iso-Butanol on Photosynthetic Electron Transport Activity in Isolated Spinach Chloroplasts)

  • 박강은
    • Journal of Plant Biology
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    • 제35권3호
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    • pp.247-252
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    • 1992
  • iso-Butanol이 엽록체의 광합성 전자전달 활성에 미치는 영향을 연구하기 위하여 암조건하에서 시금치의 엽록체에 iso-butanol을 처리한 후 대조구와 비교하여 광계 II 활성과 광계 I 활성을 조사하였으며, 또한 iso-butanol이 틸라코이드 막단백질에 미치는 영향을 알아보기 위해 전기영동으로 틸라코이드 막단백질의 변화를 조사하였다. 광계 I 활성은 iso-butanol이 저농도(1-4%)일 때는 증가하였으나 고농도(5-9%) 에서는 감소되었다. 광계 II 활성은 iso-butanol의 농도가 0.6, 0.8, 1%에서는 각각 75%, 55% 및 25%로 활성이 감소하였다. Butanol 중에서 탄소수는 같으나 OH 기의 위치가 다른 1-butanol, sec-butanol, tert-butanol, iso-butanol이 광계 II의 전자전달계에 미치는 영향을 비교해 본 결과 OH 기를 중심으로 탄소의 배열이 직선상 일 때 저해효과가 크다는 것을 알 수 있었다. iso-butanol이 1차적으로 광계 II에 미치는 억제 부위는 0.8% iso-butanol 처리구에 DPC 첨가했을 때 DCIP 환원율이 93%로 증가하는 것으로 보아 광계 II의 산화 부위임을 알 수 있다. 0.8% iso-butanol 처리구에 외부에서 망간과 칼슘을 첨가하였을 때 광계 II 활성이 각각 83%와 79%로 보호된 것으로 보아 광계 II 활성 억제는 망간의 소실과 관계 있는 것으로 생각된다. 또한 1% iso-butanol 처리한 엽록체를 20배 희석하였을 때 활성이 78%로 회복되었다. iso-Butanol은 1% 이하의 저농도에서 광계 II 활성을 감소시킨데 비해 1% iso-butanol 처리구의 틸라코이드 막단백질의 SDS-PAGE에 의한 band pattern은 대조구와 유사하며 2% 처리구에서는 52 Kd 부근에서 미세한 band pattern의 차이가 있으며 5%의 iso-butanol 처리구의 틸라코이드 막단백질의 band는 전체적으로 많이 소실되었다. 이것으로 보아 iso-butanol은 가역적으로 광계 II의 산화부위에 관여하는 단백질에 영향을 주어 $Ca^{2+}와\;Mn^{2+}$ 이온의 친화력을 저하시켜 광계 II 활성을 억제시키고 또한 알코올의 R-group의 틸라코이드 막에 침투하여 막구조를 변형시키므로 광계 I 활성이 증가하며 고농도(5-9%)에서는 비가역적으로 막구조를 변경하여 광계 I 활성이 감소한 것으로 사료된다.

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수송용 바이오 부탄올 생산을 위한 미강발효의 최적화 (Fermentation of rice bran and defatted rice bran for butanol production using Clostridium beijerinckii NCIMB 8052)

  • 이지은;서은종;박기문;진용수
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2008년도 춘계학술대회 논문집
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    • pp.235-238
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    • 2008
  • We examined butanol fermentation by Clostridium beijerinckii NCIMB 8052 using various hydrolyzates obtained from rice bran which is one of the most abundant agricultural by-products in Korea and Japan. In order to increase the amount of fermentable sugars in the hydrolyzates of rice bran, various hydrolysis procedures were applied. Total eight different hydrolyzates were prepared using rice bran (RB) and defatted rice bran (DRB) with enzyme or acid treatment and both. Each hydrolyzate was evaluated in terms of total sugar concentration and butanol production after fermentation by C. beijerinckii NCIMB 8052. Acid treatment yielded more sugar than enzyme treatment and combined treatment with enzyme and acid yielded even more sugars as compared to single treatment with enzyme or acid. As a result, the highest sugar concentration (33 g/L) was observed from the hydrolyzate from DRB (100 g/L) with combined treatment using enzyme and acid. Prior to perform fermentation of the hydrolyzates, we examined the effect of P2 solution containing yeast extract, buffer, minerals, and vitamins on production of butanol during the fermentation. Fermentation of the hydrolyzates with or without additionof P2 was performed using C. beijerinckii NCIMB 8052 in a 1 L anaerobic bioreactor. Although the hydrolyzates RB were able to support growth and butanol production, addition of P2 solution into the hydrolyzates significantly improved cell growth and butanol production. Highest butanol production (12.24 g/L) was observed from the hydrolyzate of DRB with acid and enzyme treatment after supplementation of P2 solution.

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Fermentation of Rice Bran and Defatted Rice Bran for Butanol Production Using Clostridium beijerinckii NCIMB 8052

  • Lee, Ji-Eun;Seo, Eun-Jong;Kweon, Dae-Hyuk;Park, Ki-Moon;Jin, Yong-Su
    • Journal of Microbiology and Biotechnology
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    • 제19권5호
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    • pp.482-490
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    • 2009
  • We examined butanol fermentation by Clostridium beijerinckii NCIMB 8052 using various hydrolyzates obtained from rice bran, which is one of the most abundant agricultural by-products in Korea and Japan. In order to increase the amount of fermentable sugars in the hydrolyzates of rice bran, various hydrolysis procedures were applied. Eight different hydrolyzates were prepared using rice bran (RB) and defatted rice bran (DRB) with enzyme or acid treatment or both. Each hydrolyzate was evaluated in terms of total sugar concentration and butanol production after fermentation by C. beijerinckii NCIMB 8052. Acid treatment yielded more sugar than enzyme treatment, and combined treatment with enzyme and acid yielded even more sugars as compared with single treatment with enzyme or acid. As a result, the highest sugar concentration (33 g/l) was observed from the hydrolyzate from DRB (100 g/l) with combined treatment using enzyme and acid. Prior to fermentation of the hydrolyzates, we examined the effect of P2 solution containing yeast extract, buffer, minerals, and vitamins on production of butanol during the fermentation. Fermentation of the hydrolyzates with or without addition of P2 was performed using C. beijerinckii NCIMB 8052 in a 1-1 anaerobic bioreactor. Although the RB hydrolyzates were able to support growth and butanol production, addition of P2 solution into the hydrolyzates significantly improved cell growth and butanol production. The highest butanol production (12.24 g/l) was observed from the hydrolyzate of DRB with acid and enzyme treatment after supplementation of P2 solution.

PDMS-Zeolite 복합막을 이용한 부탄올 투과증발 (Pervaporation of Butanol from their Aqueous Solution using a PDMS-Zeolite Composite Membrane)

  • 공창인;조문희;이용택
    • Korean Chemical Engineering Research
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    • 제49권6호
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    • pp.816-822
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    • 2011
  • 투과증발법은 투과 측의 진공 유지에 필요한 전력만을 소비하기 때문에 에너지 저감 기술이며, 공비증류와 같이 제 3의 보조 화학 물질을 사용하지 않기 때문에 환경 친화 기술로 알려져 있다. 본 연구에서는 수열 합성을 통해 Silicalite-1을 합성하고 이를 PDMS 고분자에 적절한 양을 첨가하여 PDMS-zeolite 복합막을 제조하였다. 제조한 분리막을 이용하여 n-부탄올 수용액으로부터 n-부탄올을 분리하였다. 공급 수용액의 농도 변화 및 첨가한 제올라이트의 양 변화에 따른 투과증발 특성을 관찰하였다. 부탄올 농도가 매우 낮은 0.001 몰분율이 포함된 1,000 $cm^3$ 수용액을 용기로 공급하였다. 투과측의 압력을 약 0.2~0.3 torr로 유지하였다. n-부탄올의 투과플럭스는 공급된 n-부탄올의 농도가 0.015 몰분율인 실험조건에서 복합막 내의 Silicalite-1의 첨가량이 0 wt%에서 10 wt%로 증가함에 따라 14.5에서 186.3 g/$m^2$/hr로 크게 증가하였다. 이는 제올라이트 입자가 지닌 미세공 구조와 강력한 소수성으로 인하여 분리막의 분자 선택성이 4.8에서 11.8로 상당히 개선되었음을 의미한다. 이러한 결과로 투과된 투과물 내의 n-부탄올의 농도가 0.07 몰분율에서 0.15 몰분율로 상당히 증가함을 알 수 있었다. 이렇게 합성된 복합막을 n-부탄올 농도가 0.015 몰분율 이하의 상당히 낮은 발효액으로부터 분리 회수하는데 유용하게 활용될 수 있을 것으로 사료된다.

톨루엔과 2-부탄올 계의 최소자연발화온도의 측정 및 예측 (Prediction and Measurement of Autoignition Temperature of Toluene and 2-Butanol System)

  • 하동명
    • 한국안전학회지
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    • 제30권4호
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    • pp.73-78
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    • 2015
  • The autoignition temperatures(AIT) of solvent mixture is important index for the safe handling of flammable liquids which constitute the solvent mixtures. Therefore, the AITs of common pure chemical substances are widely reported, but very limited data are available for mixtures. This study, the toluene and 2-butnaol system which used mixture solution solvent was measured the AIT and ignition delay time by using ASTM E659 apparatus. The AITs of toluene and 2-butanol constituted binary system were $547^{\circ}C$ and $400^{\circ}C$, respectively. The experimental AIT of toluene and 2-butanol were a good agreement with the calculated AIT by the proposed equations with a few average absolute deviation(A.A.D.).

단분산 $Al_2O_3-ZrO_2$ 복합분말의 합성과 소결특성 (Preparation and Sintering Behavior of Monodispersed Alumina-Zirconia Fine Powders)

  • 부재필;송용원;최상홀
    • 한국세라믹학회지
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    • 제31권10호
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    • pp.1209-1217
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    • 1994
  • Monodispersed alumina-zirconia fine powders were prepared by controlled hydrolysis of alkoxides. These powders and the sintered bodies were characterized. Aluminium alkoxide and zirconium alkoxide were dissolved into complex solvent with butanol and n-propanol, and by acetonitrile added hydrolytic solution, hydrolysis rate was controlled. The oil, as a dispersant, was added in hydrolytic solution, and then prepared powders were nano-sized and well-monodispersed. In the case of hydroxypropyl celluose (HPC) as a dispersant, it was added in complex solution with butanol and iso-propanol, sub-micrometer sized and well-monodispersed powders could be prepared. The value of relative density (R.D.) and tetragonal phase fraction of zirconia in the sintered body made by nano-meter sized powders were respectively higher than those in the case of sub-micrometer sized one.

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이소프로판올과 이소부탄올 용매에서의 YBCO 분말 영동전착 (Electrophoretic Deposition of YBCO powder in mixed suspension solution of iso-prophanol and iso-buthanol)

  • 소대화;이영매;박정철;코로보바
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2001년도 추계학술대회 논문집 Vol.14 No.1
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    • pp.288-291
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    • 2001
  • It is very important to select suspension solution for forming electrophoretic deposited YBCO thick mm, because it is heavily affected to its superconducting properties. In this paper, high-temperature superconductor films of $YBa_{2}Cu_{3}O_{7-x}$ were fabricated by electrophoretic deposition (EPD) from alcohol-based suspension such as iso-propanol, iso-butanol, and their mixture. For the formation of YBCO dense and adherent coating on a silver wire by EPD, 1 % PEG(1000) 2 ml, as a additive for making their surface crack-free, was used for electrophoresis. As a results, the cracks were considerably decreased and the superconducting critical current density $(J_e)$ without/with PEG was $1200A/cm^2$ and $2020A/cm^2$, which films deposited in mix iso-propanol and iso-butanol suspension.

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이소프로판올과 이소부탄을 용매에서의 YBCO 분말 영동전착 (Electrophoretic Deposition of YBCO powder in mixed suspension solution of iso-prophanol and iso-buthanol)

  • 소대화;이영매;박정철
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2001년도 추계학술대회 논문집
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    • pp.288-291
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    • 2001
  • It is very important to select suspension solution for forming electrophoretic deposited YBCO thick film, because it is heavily affected to its superconducting properties. In this paper, high-temperature superconductor films of YBa$_2$Cu$_3$$O_{7-x}$ were fabricated by electrophoretic deposition (EPD) from alcohol-based suspension such as iso-propanol, iso-butanol, and their mixture. For the formation of YBCO dense and adherent coating on a silver wire by EPD, 1% PEG(1000) 2 $m\ell$, as a additive for making their surface crack-free, was used for electrophoresis. As a results, the cracks were considerably decreased and the superconducting critical current density (J$_{c}$) without/with PEG was 1200 A/$\textrm{cm}^2$ and 2020 A/$\textrm{cm}^2$, which films deposited in mix ism-propanol and iso-butanol suspension.ion.

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소수성 ZSM-5 제올라이트 분리막을 이용한 n-부탄올/물 혼합물의 투과증발 (Pervaporation of n-Butanol/water Mixture through Organophilic ZSM-5 Zeolite Membrane)

  • 조문희;공창인;이용택
    • 멤브레인
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    • 제21권4호
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    • pp.336-344
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    • 2011
  • 소수성 ZSM-5 분리막을 결정성장핵의 수열합성 2차 성장법으로 다공성 스테인레스 스틸 지지체의 안쪽에 합성하였으며, 이렇게 제조한 분리막을 이용하여 n-부탄올 수용액으로부터 n-부탄올을 선택적으로 분리하였다. 공급 수용액의 농도 변화 및 운전 온도의 변화에 따른 투과증발 특성을 관찰하였다. 공급 수용액 내의 n-부탄올 농도를 각각 0.001, 0.005, 0.01 그리고 0.015 몰분율로, 운전 온도는 25C, $35^{\circ}C$ 그리고 $45^{\circ}C$로 바꾸면서 실험하였다. 운전 온도가 $45^{\circ}C$인 실험조건에서 공급측 n-부탄올의 몰분율이 0.001에서 0.015로 증가함에 따라 n-부탄올의 플럭스는 약 $2g/m^2/hr$ 에서 $27g/m^2/hr$ 로 크게 증가하였다. 이 결과로 투과물 내의 n-부탄올의 농도가 0.0016 몰분율에서 0.052 몰분율로 상당히 증가함을 알 수 있었다. 공급 농도가 0.015인 상태에서 운전 온도가 $25^{\circ}C$에서 $45^{\circ}C$로 증가함에 따라 n-부탄올의 플럭스는 약 $13g/m^2/hr$ 에서 $27g/m^2/hr$ 로 크게 증가하였으며, 투과물 내의 n-부탄올 농도도 따라서 0.045에서 0.052로 증가함을 관찰할 수 있었다.

공비혼합물로 제조된 다공성 센서재료용 실리카 에어로젤 (Silica aerogels for potential sensor material prepared by azeotropic mixture)

  • 안나 쉴랴흐티나;오영제
    • 센서학회지
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    • 제16권6호
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    • pp.395-400
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    • 2007
  • Ambient drying sol-gel processing was used for monolithic silica ambigels in the temperature range of $130-250^{\circ}C$. A new method of mesopore ambigels, which mean the aerogels prepared by ambient pressure drying process synthesis, is suggested at first. This method includes two important approaches. The first point is that $SiO_{2}$ surface modification of wet gel was performed by trimethylchlorosilane in n-butanol solution. This procedure is provided the silica gel mesopore structure formation. The second point is a creation of the ternary azeotropic mixture water/n-butanol/octane as porous liquid, which is effectively provided removing of water such a low temperature by 2 step drying condition under ambient pressure. The silica aerogels, which were prepared by ambient pressure drying from azeotropic mixture of water/n-butanol/octane, are transparent, crack-free and mesoporous (pore size ${\sim}$ 5.6 nm) with surface area of ${\sim}$ $923{\;}m^2/g$, bulk density of $0.4{\;}g/cm^3$ and porosity of 85 %.