• 제목/요약/키워드: successive reaction.

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황화납/산화아연 나노선을 이용한 양자점 감응형 태양전지 (Quantum Dot Sensitized Solar Cell Using PbS/ZnO Nanowires)

  • 김우석;용기중
    • 청정기술
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    • 제16권4호
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    • pp.292-296
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    • 2010
  • 황화납(PbS)을 감응물질로 하는 양자점 감응형 태양전지를 제작하고 효율을 측정해 보았다. 기판에 산화아연(ZnO) 나노선을 기른 후 SILAR(Successive ionic layer adsorption and reaction)법으로 PbS 양자점을 합성하고 이를 주사전자현미경(SEM), X-선 회절(XRD)을 통해 확인하였다. SILAR를 통해서 형성된 나노이종구조는 PbS 나노입자들이 ZnO 나노선 위에 균일하게 성장한 것을 확인할 수 있었다. 본 실험에서 PbS을 이용한 양자점 감응형 태양전지의 최고 효율은 one sun에서 0.075%로 나타났으며, 이는 기존의 다른 감응 물질에 비해 비교적 낮은 효율을 나타내었다. 이러한 요인으로는 i) ZnO와 PbS의 밴드갭 배열이 Type-I 형을 이룰 수 있는 가능성, ii) 다양한 크기의 밴드갭을 가지는 PbS에 의한 전자이동 방해 효과, iii) 전해질에 의한 PbS의 안정성 저하 등의 이유를 생각해 볼 수 있으며, 이를 해결하기 위해서는 PbS의 크기분포 조절과 새로운 전해질에 대한 연구가 향후 필요할 것으로 생각된다.

대곡(大谷) W-Sn-Cu 광상(鑛床)의 열수변질작용(熱水變質作用) (Wall-rock Alteration Relating to Tungsten-Tin-Copper Mineralization at the Ohtani Mine, Japan)

  • 김문영
    • 자원환경지질
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    • 제21권3호
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    • pp.209-221
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    • 1988
  • The ore deposit of the Ohtani mine is one of repesentatives of plutonic tungsten-tin veins related genetically to acidic magmatism of Late Cretaceous in the Inner zone of Southwest Japan. Based on macrostructures of vein filling on the order of ore body, three major mineralization stages, called stage I, stage II, and stage ill from earliest to latest, are distinguished by major tectonic breaks. The alteration zories are characterized by specific mineral associations in pseudomorphs after biotite. The alteration zones can be divided into two parts, i. e. a chlorite zone and a muscovite zone, each repesenting mineralogical and chemical changes produced by the hydrothermal alteration. The chloritic alteration took place at the beginning of mineralization, and muscovite alteration in additions to chloritic alteration took place at stage II and ill. The alteration zones are considered to be formed by either of two alteration mechanism. 1) The zones are formed by reaction of the rock with successive flows of solution of different composition and different stage. 2) The zones are formed contemporaneously as the solution move outward. Reaction between the solution and the wall-rock results in a continuous change in solution chemistry. The migration of the successive replacement of the fresh zone$\rightarrow$the chlorite zone$\rightarrow$the muscovite zone may have transgressed slowly veinward, leaving metasomatic borders between the different zones.

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$(\pm)$-2-[p-(1-Oxo-2-isoindolinyl)phenyl]butyric acid(인도부펜)의 합성 (Facile Synthesis of $(\pm)$-2-[p-(1-Oxo-2-isoindolinyl)phenyl]butyric acid (Indobufen))

  • 최홍대;강병원;마정주;윤호상
    • 약학회지
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    • 제35권5호
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    • pp.389-393
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    • 1991
  • A convenient method for the synthesis of indobufen, which is a potent antiinflammatory agent, was described. Ethyl 2-phenylbutyrate(4) was prepared by Friedel-Crafts reaction of benzene with ethyl $\alpha$-chloro-$\alpha$-(methylthio)acetate(l) followed by ethylation and desulfurization of the resultant ethyl 2-(methylthio)phenylacetate(2). Ethyl 2-(p-aminophenyl)butyrate(6) was prepared by nitration of (4) and successive reduction of ethyl 2-(p-nitrophenyl) butyrate(5). Indobufen was obtained by condensation reaction of (6) with phthalic anhydride followed by reduction and hydrolysis of the resultant ethyl 2-[p-(1, 3-dioxo-2-isoindolinyl)phenyl]butyrate(7).

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In Situ X-ray Absorption Spectroscopic Study for α-MoO3 Electrode upon Discharge/Charge Reaction in Lithium Secondary Batteries

  • Kang, Joo-Hee;Paek, Seung-Min;Choy, Jin-Ho
    • Bulletin of the Korean Chemical Society
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    • 제31권12호
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    • pp.3675-3678
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    • 2010
  • In-situ X-ray absorption spectroscopy (XAS) was used to elucidate the structural variation of $\alpha-MoO_3$ electrode upon discharge/charge reaction in a lithium ion battery. According to the XAS analysis, hexavalent Mo atoms in $\alpha-MoO_3$ framework are reduced as the amount of intercalated lithium ions increases. As lithium de-intercalation proceeds, most of pre-edge peaks are restored again. However, according to the Fourier transforms of the extended X-ray absorption fine structure (EXAFS) spectra, lithium de-intercalation reaction is partially irreversible upon the charge reaction, which is one of the main reasons why the capacity of $\alpha-MoO_3$ electrode decreases upon successive discharge/charge cycles.

2-(p-메틸알릴아미노페닐)프로판산의 합성 (Facile Synthesis of 2-(p-Methylallylaminophenyl)propionic Acid (Alminoprofen))

  • 최홍대;윤호상;강병원;마정주;손병화
    • 약학회지
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    • 제36권1호
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    • pp.12-16
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    • 1992
  • A new method for the synthesis of alminoprofen, which is a non-steroidal antiinflammatory agent, was described. Ethyl 2-phenyl-propionate(4) was prepared by Friedel-Crafts reaction of benzene with ethyl ${\alpha}-chloro-{\alpha}(methylthio)acetate(1)$, followed by methylation and desulfurization of the resultant ethyl 2-(methylthio)phenylacetate(2). Ethyl 2-(p-aminophenyl)propionate(6) was obtained by nitration of (4) and successive reduction of ethyl 2-(p-nitrophenyl)propionate(5). Alminoprofen was synthesized by reaction of (6) with methallyl chloride, followed by hydrolysis of the resultant ethyl 2-(p-methylallylaminophenyl)propionate (7).

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Preparation of CdS-pillared $H_4Nb_6O_7$ and Photochemical Reduction of Nitrate under Visible Light Irradiation

  • Tawkaew, Sittinun;Fujishiro, Yoshinobu;Uchida, Satoshi;Sato, Tsugio
    • The Korean Journal of Ceramics
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    • 제6권1호
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    • pp.43-46
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    • 2000
  • $H_4Nb_6/O_{17}$/CdS nanocomposites which intercalated CdS particles, less than 0.8nm thickness, in the interlayer of $H_4Nb_6/O_{17}$ were prepared by the successive ion exchange reactions of $H_4Nb_6/O_{17}$ with $Cd^{2+}$ and $C_3H_7NH_3_+$, followed by the reaction with $H_2S$ gas. $H_4Nb_6/O_{17}$/CdS photocatalytically reduced $NO_3$ ̄ to $NO_2$ ̄ and $NH_3$in the presence of sacrificial hole acceptor such as methanol under visible light irradiation (wavelength>400nm), although unsupported CdS showed no noticeable photocatalytic activity for $NO_3$ ̄ reduction. The catalytic activity of $H_4Nb_6/O_{17}$/CdS greatly enhanced with co-doping of Pt particles in the interlayer.

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주쇄형이량체액정의 상도와 분자형태 (Phase Diagrams of Binary Mixtures Comprising Main-Chain Dimer Liquid Crystals and Molecular Ordering)

  • 남수용
    • 한국인쇄학회지
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    • 제16권2호
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    • pp.61-74
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    • 1998
  • Some photopolymer, poly(vinyl cinnamoyl acetate)(PVCiA) was synthesized by esterification of polymer(vinyl alcohol)(PVA) with monochloroacetic acid, followed by reaction poly(vinyl monochloroacetate)(PVAhA) and potassium cinnamate. When esterification of PVA with monochloroacetic acid was reacted in the dimethyl sulfoxide(DMSO), in the synthesis of PVChA, it is very good yield and the successive cinnamoyl acetoxyl esterification of PVCiA can be successfully synthesized. But PVCiA is low photosensitive polymer if net added photosensitizing dyes. Here, we synthesized photosensitizing dyes.

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Anti-allergy Activity of Cinnamomi Cortex

  • Kim, Ra-Min;Kim, Young-Hee;Lee, Eun-Bang
    • Natural Product Sciences
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    • 제6권1호
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    • pp.49-51
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    • 2000
  • The anti-allergy activity of Cinnamomum cassia cortex extract and its fractions were investigated in mice. The extract exhibited potent anaphylactic shock and Arthus reaction. Among the fractions obtained in the successive fractionation with n-hexane, butanol and acetone, the butanol insoluble portion was shown to have the activities.

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Acceptor reaction of a novel transfructosylating enzyme from Bacillus sp.

  • 김영미;;박종필;윤종원
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2000년도 추계학술발표대회 및 bio-venture fair
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    • pp.583-586
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    • 2000
  • Many different oligosaccharides were produced by transferring the fructose residue of sucrose to maltose, cellobiose, lactose and sucrose (self-transfer), where their yields of fructosylated acceptor products accounted for $26{\sim}30%$ (w/w). The maximum conversion yield (30%) was obtained in fructosyl cellobioside formation with 500 g sucrose/l (substrate) and 200 g cellobiose/l (acceptor). These four acceptors gave various products having DP (degree of polymerization) $2{\sim}7$ by successive transfer reactions.

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팔라듐 촉매하 결합반응을 이용한 플루비프로펜의 간결한 합성 (Concise Synthesis of Flurbiprofen via Palladium-Catalyzed Cross-Coupling Reactions)

  • 한영택
    • 약학회지
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    • 제59권2호
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    • pp.66-69
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    • 2015
  • A concise synthesis of flurbiprofen, a member of the non-steroidal anti-inflammatory 2-arylpropionic acids, has been accomplished. The key feature of this synthesis involves successive palladium-catalyzed cross coupling reactions. In particular, a 2-arylacylate intermediate, which easily converted to the key 2-arylpropionic acid scaffold, was afforded by a versatile palladium-catalyzed cross coupling reaction between diazopropanate and bisphenylboronic acid. This synthetic procedure would facilitate synthesis of the flurbiprofen and anti-inflammatory 2-arylpropionic acid derivatives.