• Title/Summary/Keyword: aniline

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Fluorescence probe study on the solubilization sites of aniline derivatives in triton X-100 and zephiramine micelles

  • Han, Suk-Kyu;Lee, Yong-Soo
    • Archives of Pharmacal Research
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    • v.9 no.3
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    • pp.139-144
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    • 1986
  • The solubilization sites of aniline and its derivatives in micelles were investigated with fluorescence probe technique. The fluorescence probes employed in this study are 12-(9-anthroyl) stearic acid (AS) and 2-p-toluidinylnaphthalene-6-sulfonate (TNS) which are incorporated in the interior of the micelle and attaced to its surface, respectively. As these two probes were effectively quenched by aniline and its surface, respectively. As these two probes were effectively quenched by aniline and its derivatives, the modified Stern-Volmer relationship in micellar system could be applicable to estimate the partition coefficient, $K_{p}$ of the solubilizate between aqueous and micellar phase. Because $K_{p}$ derived by this method reflects the relative proximity of the fluorophore to the quencher, the ratio of $K_{p}$ in the surface area to that in the interior of the micelle is interpreted in terms of the relative location of the solubilizate in micellar aggregate. The results show that the solubilizates are not located in a definite position but distributed in the multiple-sites of the micelle. The solubilization sites of the solubilizates in the icelle are dependent on their structures. As the solubilizate has more numbers of N-substituents of aniline and more numbers, of carbon in the substituent, it tends to incorporate in the interior of the micelle more effectively.

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Effect of Dual Substrates on Aniline Mineralization by Pseudomonas testosteroni 6F1 (Pseudomonas testosteroni 6F1의 아닐린 분해에 미치는 이차기질의 영향)

  • Cho, Kyung-Yun;Chun, Hyo-Kon;Bae, Kyung-Sook;Kho, Young-Hee
    • Microbiology and Biotechnology Letters
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    • v.16 no.5
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    • pp.427-431
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    • 1988
  • The simultaneons mineralization of aniline and other secondary carbon sources by Pseudomonas testosteroni 6Fl were evaluated by the lag time and the enzyme induction level. The lag time for aniline mineralization by P. testosteroni 6Fl was 7 hours, whereas the lag time for aniline and readily utilizable secondary substrates were 1-3 hours. This stimulated degradation resulted from the simultaneous use of secondary substrates and aniline, the increased rate of enzyme induction, and the in-creased rate of the cell growth. The enzyme induction level of P. testosteron 6F1 were varied according to the kinds of secondary substrate.

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Preparation of Antistatic Coating Solutions by Blending Aniline Terminated Waterborne Polyurethane with PEDOT/PSS (Aniline Terminated Waterborne Polyurethane과 PEDOT/PSS의 블렌딩에 의한 대전방지 코팅용액의 제조)

  • Hong, Min Gi;Huh, Woo Young;Byun, Tae Gang;Song, Ki Chang
    • Korean Chemical Engineering Research
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    • v.50 no.4
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    • pp.614-620
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    • 2012
  • Polyurethane prepolymers were prepared from poly (carbonate diol), isophrone diisocyanate and dimethylol propionic acid. Then, aniline terminated waterborne polyurethane dispersion (ATPUD) was synthesized by capping the NCO group of the prepolymer with aniline monomer. Subsequently, ATPUD and waterborne polyurethane dispersion (PUD), respectively, were blended with conducting polymer, poly (3,4-ethylenedioxythiophene)/polystyrene sulfonate [PEDOT/PSS], to yield antistatic coating solutions, and the mixture was coated on the polycarbonate substrates. At adequate addition amounts of PEDOT/PSS less than or equal to 2.5 g, the surface resistances ($1.0{\times}10^{11}{\sim}2.5{\times}10^8{\Omega}/cm^2$) of coating films from ATPUD showed better electronic conductivities than those ($5.0{\times}10^{11}{\sim}6.3{\times}10^9{\Omega}/cm^2$) from PUD. However, at excess amount of PEDOT/PSS of 3.0 g, the surface resistance from ATPUD showed similar electronic conductivity with that from PUD.

Development of Fusant Degrading Aniline and 4-chlorobiphenyl by Spheroplast Fusion between Pseudomonas sp. and Flavimonas oryzihabitans (Flavimonas oryzihabitans와 Pseudomonas sp.간 원형질체 융합에 의한 Aniline과 4-chlorobiphenyl 분해균주 개발)

  • 박형수;박용근;김무훈;고범준;조미영;김치경
    • Korean Journal of Microbiology
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    • v.36 no.4
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    • pp.259-266
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    • 2000
  • Spheroplast cell fusions were performed with Flavimonas oryzihabitans degrading aniline and Pseudomonas sp. degrading 4-chlorobiphenyl to develope the new fusant degrading aniline and 4-CBP and its characters were investigated. F. oryzihabitans was induced to antibiotic marker ($Cm^r$ by NTG treatment for the fusants selection. The results of spheroplast formation and regeneration frequencies of the strains treated with lysozyme-EDTA were 99% and 5.0~6.6%, respectively. Fusion products were treated with 40% (v/v) PEG 6000 and fusion frequency was $3.16{\times}10^{-4} $. The DNA content of fusant, F22 was approximately 2-fold compared with parents. The fusant was stable, and showed the mixed biochemical characteristics of the parent strains. F22 was similar to parent for cell growth pattern and degrading capacity on 5 mM aniline but cell growth rate of F22 was 1.5-fold higher than that of the parent on 10mM aniline. However 4-CBP degrading ability of F22 was slightly lower than that of parental strain.

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The Effects of Tungsten Electrode on Electrochemical Synthesis of Polyaniline (텅스텐 전극이 폴리아닐린의 전기화학적 중합에 미치는 영향)

  • Jung-Kyoon Chon;Byoung Hoon Min
    • Journal of the Korean Chemical Society
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    • v.38 no.12
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    • pp.885-890
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    • 1994
  • Kinetics of electrochemical polymerization of aniline on a tungsten electrode in acidic aqueous solution was studied by means of cyclic voltammetry and kinetic measurements of anodic oxidation. Aniline molecule appeared to be intially oxidized via two-electron transfer to produce oxidized deprotonated aniline ion, which subsequently undergoes nucleophilic attack to the parent aniline and results in head to tail coupling to yield a dimerized species. But, being contrary to the case of Pt electrode, the propagation of polymerization occured through attack of the monomer by the oxidized aniline monomer to polymer. The growth rate of polyaniline was slow in comparison with the growth on Pt electrode. The degradation products were confirmed to be not p-benzoquinone(BQ) but p-phenylenediamine(p-PDA) by spectrophotometry, which agrees with the fact that oxidation of p-PDA was not observed below 1.0 V.

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Cinnamic Acid Derivatives IV, The Kinetics and Mechanism of the Hydrolysis of Cinnamylidene aniline Derivatives (신남산 유도체 Ⅳ, Cinnamylidene anilin 유도체의 가수분해 반응에 대한 메카니즘과 그 반응속도론적 연구)

  • Lee, Gi-Chang;Park, Su-In;Hwang, Yong-Hyeon;Lee, Gwang-Il;Choe, Bong-Jong;Jeong, Deok-Chae
    • Journal of the Korean Applied Science and Technology
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    • v.8 no.1
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    • pp.1-7
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    • 1991
  • The kinetic of hydrolysis for cinnamylidene aniline derivatives has been investigated by ultraviolet spectrophotometry in 20% (v/v) dioxane - $H_2O$ at $25^{\circ}C$. A rate equation which can be applied over wide pH range was obtained. The substituent effects on cinnamylidene aniline derivatives were studied and the hydrolysis was facilitated by electron attracting group. Final products of the hydrolysis were cinnamaldehyde and aniline. From the rate equation, substituent effect and final products, the hydrolysis of cinnamylidene aniline derivatives was initiated by the neutral molecule of $H_2O$ which does not dissociate at below pH 9.0${\sim}$12.0, but proceeded by the hydrogen ion at above pH 5.0${\sim}$9.0.

Micellar Catalysis on the Hydrolysis of the Fungicidal N-[1-(benzotriazol-1-yl)benzyl]aniline (항균성, N-[1-(benzotriazol-1-yl)benzyl]aniline의 가수분해 반응에 미치는 미셀 촉매효과)

  • Sung, N.D.;Park, C.K.;Lim, C.W.
    • Applied Biological Chemistry
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    • v.37 no.3
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    • pp.189-193
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    • 1994
  • The hydrolysis of fungicidal N-[1-(benzotriazol-1-yl)benzyl]aniline (BBA) molecule in the presence of cationic cetyltrimethylammonium bromide (CTABr) and anionic sodium laurylsulfate (NaLs) micellar solutions has been studied kinetically. The Micellar catalysis effect shows that the rate is slightly accelerated by the addition of the anionic NaLs at high pH and the binding constant (Ks) is $1.45{\times}10^4M^{-1}$. This result presumably is due to the electrostatic stabilization by the anionic micelle of the developing carbocation in the transition state rather than the hydrophobic character (${\pi}$: 4.93) of (BBA).

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Tempereture Dependent Dielectric Relaxation Study of Aniline in Dimethylsulphoxide and Dimethlformamide Using Time Domain Technique (시간분해기법을 이용한 디메틸 술폭사이드와 디메틸 포름아미드-아닐린용액에서 온도의존 유전이완에 관한 연구)

  • Chaudhari, Ajay;Patil, C.S.;Shankarwar, A.G.; Arbad, B.R.;Mehrotra, S.C.
    • Journal of the Korean Chemical Society
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    • v.45 no.3
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    • pp.201-207
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    • 2001
  • The dielectric relaxation study for aniline-dimethylsulphoxide (DMSO) and aniline-dim.ethylformamide(DMF) has been carried out using the Time domain reflectometry (TDR) technique, at different temperature and concentrations, in the frequency range of 10 MHz to 10 GHz. The dielectric parameters viz. static permittivity, relaxation time, the Kirkwood correlation factor, excess permittivity, excess inverse relaxation time and thermodynamic parameters have been obtained. The calibration method based on least squares fit method has been used. The dielectric parameters show systematic change with temperature and concentrations.

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Synthesis of 2,6-dichloro-4-Nitro Aniline Mercuric Acetate and Its Pharmaceutical Effects (2,6 dichloro-4-Nitro Aniline Mercuric Acetate의 合成과 그 藥劑效果에 관한 硏究)

  • Cho, Chul-Hyung;Shin, Sung-Euy
    • Journal of the Korean Chemical Society
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    • v.14 no.3
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    • pp.207-212
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    • 1970
  • A large variety of weed killers, insecticides, and bactericiedes on the market today are of almost infinite variety, but their pharmacological effects are different from each other according to the objects to cope with. Therefore, it is hoped that some chemical substance which serves as weed killer, an insecticide, and a bactericede at a same time, should be synthesized, in order to save expense and labor. I anticipated that the desire would be met by introducing to a molecule the radical which has the three effects. Here, I made an attempt of introducing $Cl_2$ gas to aniline considering the following respects: 1. Introduction velocity of $Cl_2$ gas under the varied temeratures and velocities of $Cl_2$ gas 2. The effect of reaction period under the condition which gives the most satisfactory yield. 3. The actions of catalysts, $SbCl_3$, $FeCl_3$, and $MoCl_5$, and their proportions when a mixture of the three catalysts is used in producing 2,6-dichloro-aniline. After consideration of above phenomena, the maximum production rate of 79.5% of 2.6-compound was obtained. With the compound I synthesized 2.6-dichloro-4-nitroaniline-mercuric acetate. Investigations of the effects of the compound as weed killer, an insecticide, and a bactericide showed that the compound, 2,6-dichloro-4-Nitro Aniline mercuric acetate has a satisfactory herbi-insecti-bactericidal effect.

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The Influence of Aniline to Acid Composition on the Electrical Conductivity of PANI-PAAMPSA

  • Yoo, Joung Eun;Bae, Joonho
    • Bulletin of the Korean Chemical Society
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    • v.34 no.12
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    • pp.3825-3828
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    • 2013
  • In this study, the influences of aniline to acid composition were investigated on the electrical conductivity of PANI-PAAMPSA. The ratio of aniline to sulfonic acid groups was optimized for the maximum conductivity of PANI-PAAMPSA. The conductivity is strongly correlated with the electronic structure of PANI-PAAMPSA; the highest conductivity of PANI-PAAMPSA was observed when PANI has the longest conjugation length.