• 제목/요약/키워드: Perchlorate

검색결과 249건 처리시간 0.025초

Voltammetric Studies of Anion Transfer Reactions Across a Microhole Array-Water/PVC-NPOE Gel Interface

  • Hossain, Md. Mokarrom;Girault, Hubert H.;Lee, Hye-Jin
    • Bulletin of the Korean Chemical Society
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    • 제33권5호
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    • pp.1734-1740
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    • 2012
  • Voltammetric characterization of hydrophilic anion transfer processes across a 66 microhole array interface between the water and polyvinylchloride-2-nitrophenyloctylether gel layer is demonstrated. Since the transfer of hydrophilic anions including $Br^-$, $NO_3{^-}$, $I^-$, $SCN^-$ and $ClO_4{^-}$ across the liquid/gel interface usually sets the potential window within a negative potential region, a highly hydrophobic organic electrolyte, tetraoctylammonium tetrakis(pentafluorophenyl)borate, providing a wider potential window was incorporated into the gel phase. The transfer reaction of perchlorate anions across the microhole-water/gel interface was first studied using cyclic voltammetry and differential pulse voltammetry. The full voltammetric response of perchlorate anion transfer was then used as a reference for evaluating the half-wave transfer potentials, the formal transfer potentials and the formal Gibbs transfer energies of more hydrophilic anions such as $Br^-$, $NO_3{^-}$, $I^-$, and $SCN^-$. The current response associated with the perchlorate anion transfer across the micro-water/gel interface versus the perchlorate concentration was also demonstrated for sensing applications.

Ormosil에 침투된 Rhodamine 6G Perchlorate의 이중합체의 검출 (Detection of Dimer of Rhodamine 6G Perchlorate Doped in Ormosil)

  • 김구대;이동아;문지웅;박경수
    • 분석과학
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    • 제10권3호
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    • pp.225-229
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    • 1997
  • 졸겔법에 의해 제조된 organically modified silicate(Ormosil)에 Rhodamine 6G perchlorate(Rh6GP)를 침투시켰으며, 이 유기염료가 무기/유기 복합 기저체(host)에 안정하게 침투되었는지를 확인하였다. 복합졸의 상태에서 측정된 유기염료의 흡수스펙트럼과 겔화된 후의 스펙트럼, 그리고 복합체가 완전히 건조된 상태에서의 스펙트럼을 비교하여 Rh6GP가 이합체화되지 않고 안정한 상태로 있을 수 있는 Ormosil의 조성을 확립하였다. 졸겔반응시의 촉매로 사용된 염산의 농도가 Tetraethyl orthosilicate(TEOS) 1몰을 기준으로 0.1몰 이내의 범위에서만 유기염료가 안정하고 이합체화되지 않은 상태가 유지되었다.

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영가철 나노 입자가 전착된 다공성 탄소전극을 이용한 과염소산 이온의 전기화학적 환원 (Electrochemical Reduction of Perchlorate Ion on Porous Carbon Electrodes Deposited with Iron Nanoparticles)

  • 이인숙;김은영;이보경;팽기정
    • 전기화학회지
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    • 제18권2호
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    • pp.81-85
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    • 2015
  • A method for degradation of the perchlorate anion ($ClO{_4}^-$) has been studied using electrochemically generated zero-valent iron (ZVI) deposited on a porous carbon electrode. The first strategy of this study is to produce the ZVI via the electrochemical reduction of iron (II) on a porous carbon electrode coated with a conducting polymer, instead of employing expensive $NaBH_4$. The present method produced well distributed ZVI on conducting polymer (polypyrrole thin film) and increased surface area. ZVI surface can be regenerated easily for successive reduction. The second strategy is to apply a mild reducing condition (-0.3 V) to enhance the efficiency of the degradation of perchlorate with ZVI without the evolution of hydrogen. The electrochemically generated ZVI nanoparticles may offer an alternative means for the complete destruction perchlorate without evolution of hydrogen in water with high efficiency and at low cost.

Polymeric Membrane and Solid Contact Electrodes Based on Schiff Base Complexes of Co(III) for Potentiometric Determination of Perchlorate Ions

  • Soleymanpour, Ahmad;Hanifi, Abdolghafoor;Kyanfar, Ali Hossein
    • Bulletin of the Korean Chemical Society
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    • 제29권9호
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    • pp.1774-1780
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    • 2008
  • New PVC based polymeric membrane electrodes (PME) and coated glassy carbon electrodes (CGCE) based on synthesized Schiff base complexes of Co(III); [Co(Salen)$(PBu_3)_2$]$ClO_4$, [Co($Me_2$Salen)$(PBu_3)_2$]$ClO_4$, [Co(Salen)$(PBu_3)H_2O$]$ClO_4$; as anion carriers for potentiometric determination of $ClO_4\;^-$were studied. The PME and also CGCE electrodes prepared with [Co(Me2Salen)$(PBu_3)_2$]$ClO_4$ showed excellent response characteristics to perchlorate ions. The electrodes exhibited Nernstian responses to $ClO_4\;^-$ ions over a wide concentration range with low detection limits ($1.0 {\times} 10^{-6}\;mol\;L^{-1}$ for PME and $9.0 {\times} 10^{-7}\;mol\;L^{-1}$ for CGCE). The electrodes possess fast response time, satisfactory reproducibility, appropriate lifetime and, most importantly, good selectivity toward $ClO_4\;^-$ relative to a variety of other common inorganic anions. The potentiometric response of the electrodes is independent of the pH in the pH range 2.5-8.5. The proposed sensors were used in potentiometric determination of perchlorate ions in mineral water and urine samples. The interaction of the ionophore with perchlorate ions was shown by UV/Vis spectroscopy.

2-phenyl-N-methyl-l,3-thiazolium Perchlorate 유도체의 합성 및 가수분해 (Synthesis and hydrolysis of 2-phenyl-N-methyl-1,3-thiazolium Perchlorate derivatives.)

  • 한만소;이소영
    • 한국응용과학기술학회지
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    • 제15권2호
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    • pp.93-99
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    • 1998
  • 2-phenyl-N-methyl-1,3-thiazolium perchlorate(PTP)derivatives were synthesized via addition and substitution reactions. PTP was hydrolyzed under aqueous hydrochloride. The structures of the compounds were conformed by N.M.R.,I.R., and elemental analysis.

An Efficient Method for Multicomponent Synthesis of Spiro[4H-pyran-oxindole] Derivatives Catalyzed by Magnesium Perchlorate

  • Wu, Chunlei;Shen, Runpu;Chen, Jianhui;Hu, Chunqi
    • Bulletin of the Korean Chemical Society
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    • 제34권8호
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    • pp.2431-2435
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    • 2013
  • A simple and efficient method for the synthesis of spiro[4H-pyran-oxindole] derivatives by means of three-component reactions between isatins, malononitrile or ethyl cyano-acetate, and 1,3-dicarbonyl compounds in the presence of catalytic amount of magnesium perchlorate in 50% aqueous ethanol medium has been described.

Reactions of Thianthrene Cation Radical Perchlorate with Free Radical. Ⅱ. On the Reaction with tert-Butyl Peroxide$^1$

  • Shin, Jong-Heon;Kim, Kyon-Gtae
    • Bulletin of the Korean Chemical Society
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    • 제5권6호
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    • pp.211-215
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    • 1984
  • Reaction of thianthrene cation radical perchlorate (1) with tert-butyl peroxide (TBP) in acetonitrile gave thianthrene (2), thianthrene 5-oxide (3), cis-thianthrene-5,10-dioxide (4), 5-acetonylthianthrenium perchlorate (9), along with small amount of thianthrene-5,5-dioxide (7) in some cases. Isolation of N-tert-butylacetamide indicated the formation of tert-butyl cation from TBP. The formation mechanisms of these products were proposed.

초미세 크기의 과염소산암모늄 결정체 제조 (Preparation of Ultra Fine Ammonium Perchlorate Crystals)

  • 김준형;임유진
    • 한국추진공학회지
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    • 제8권1호
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    • pp.1-7
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    • 2004
  • 과염소산암모늄(AP)의 N-메틸피롤리돈(NMP) 용액으로부터 초미세 크기를 갖는 과염소산암모늄(UFAP) 결정의 결정화 연구를 수행하였고, 침전된 결정들의 특성들을 scanning electron micrograph(SEM)와 X-ray diffraction(XRD) 그리고 thermogravimetric analysis(TGA)를 사용하여 분석하였다. 침전용매로 클로로포름, 염화메틸렌 그리고 톨루엔이 사용되었을 경우, 2$\mu\textrm{m}$ 이하의 크기를 갖는 결정들이 제조되었다. 제조된 UFAP의 결정학적 특성과 열분해 거동은 상용으로 사용되는 AP와 거의 유사하였다.

Citrobacter amalonatics와 Citrobacter farmari에 의한 perchlorate 환원

  • ;이일수;배재호
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 2003년도 추계학술발표회
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    • pp.438-441
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    • 2003
  • The present study reports the novel physiological function of dissimilatory perchlorate reduction by two strains JB101 and JB109 isolated from a sewage treatment facility in Incheon, South Korea. The physiological data of the isolates showed good correspondence with the members of the family Enterobacteriaceae. The partial 16S rRNA and 16S rDNA sequence of strains JB101 and JB109 showed similarity of 99.8% to Citrobacter amalonaticus and 98% to Citrobacter farmari, respectively. The study infers toward possibility of Citrobacter spp. to form an important group of dissimilatory perchlorate reducers within the (equation omitted) subclass of Proteobacteria because the majority of the known. members belong to two monophyletic groups namely Dechloromonas and Dechlorosoma in $\beta$ subclass of Proteobacteria.

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산화티탄의 광전기화학 특성을 이용한 퍼클로레이트 이온 제거 (Photoelectrochemical Degradation of Perchlorate Ions by TiO2)

  • 민형섭;이전국
    • 한국재료학회지
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    • 제18권8호
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    • pp.432-437
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    • 2008
  • Titanium oxide films and powders are attached onto carbon cloths via RF reactive sputtering and an epoxy resin mixture, respectively. $TiO_2$/carbon composite materials were used to investigate the photoelectrochemical degradation of perchlorate ions in water. The energy band gaps of the RF-sputtered $TiO_2$ thin films ranged from 3.35-3.44 eV. A photocurrent of the powdered $TiO_2$ as illuminated by ultra-violet light for 30 min. was $2.79\;mA/cm^2$. Perchlorate ions in water were shown to be degradable by a UV-illuminated $TiO_2$ powder/carbon/Nafion/carbon composite.