• Title/Summary/Keyword: LEE Myong-ki

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Clinnamic Acid Derivatives II, The Kinetics and Mechanism of the Hydrolysis of Benzalacetophenone Derivatives (신남산 유도체 II, Benzalacetophenone 유도체의 가수분해 메카니즘과 반응속도론적 연구)

  • Hwang, Yong-Hyun;Lee, Ki-Chang;Ryu, Jung-Wook;Lee, Kwang-Il;Choi, Bong-Jong
    • Journal of the Korean Applied Science and Technology
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    • v.6 no.2
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    • pp.67-74
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    • 1989
  • The Kinetics of the Hydrolysis of benzalacetophenone derivatives has been investigated by ultraviolet spectrophotometry in 5% dioxane - $H_2O$ at $50^{\circ}C$. A rate equation which can be applied over wide pH range was obtained. The substituent effect on the hydrolysis of benzalacetophenone derivatives were facilitated by electron attracting groups. Based on the rate equation, substituent effect, general base effect, activation parameters and final product, the hydrolysis of benzalacetophenone derivatives seems to be initiated by the netural molecule of $H_2O$ which does not dissociate at below pH 9.0 but proceeded by the hydroxide ion at above pH 11.0. In the range of pH $9.0{\sim}11.0$ these two reactions occur competitively.

Characteristics and Pot Test according to Blending of PVA/Algin (PVA와 Algin의 블렌딩에 따른 특성과 토양분해)

  • Cho, Hyung-Jae;Oh, Se-Young;Lee, Ki-Chang;Jung, Duck-Chea;Kim, Yong-Yeul;Hwang, Seong-Hee
    • Journal of the Korean Applied Science and Technology
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    • v.16 no.1
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    • pp.25-31
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    • 1999
  • Algin is known as biodegradable natural polymer from marine plants. PVA/Algin blend films were prepared by solution blending method for the purpose of useful biodegradable polymer. Characteristics properties of PVA/Algin blend films such as DSC, Elongation, Tensile strength and Morphological change by SEM were determined. Tensile strength and Elongation were rapidly reduced as increasing the blend ratio of Algin. PVA/Algin blend films were found that phase separation was occured as more than 25wt% increasing the blend ratio of Algin. Blend films were observed to be less partially compatibility than 10wt% increasing the blend ratio of Algin by DSC, mechanical properties and SEM. Also, PVA/Algin blend films at the laboratory soil test(Pot Test) were completely degraded in months with four kinds of soils by microorganisms.

The Kinetics and Mechanism of the Hydrolysis to Thienyl Chalcone Derivatives (Thienyl Chalcone 유도체의 가수분해 반응메카니즘과 그 반응속도론적 연구)

  • Hwang, Yong-Hyun;Lee, Ki-Chang;Kim, Jin-Yeong
    • Journal of the Korean Applied Science and Technology
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    • v.10 no.2
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    • pp.73-80
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    • 1993
  • The hydrolysis reaction kinetics of 2-thienyl chalcone derivatives $[II]{\sim}[V]$ was investigated by ultraviolet spectrophotometery in 20% dioxane-$H_2O$ at $25^{\circ}C$ and the structure of these compounds were ascertained by means of ultraviolet, infrared and NMR spectra. The rate equations which were applied over a wide pH range(pH $1.0{\sim}13.0$) were obtained. The substituent effects on 2-thienyl chalcone derivatives$[II]{\sim}[V]$ were studied, and the hydrolysis were facilitated by electron attracting groups. On the basis of the rate equation, substitutent effect and final product, the plausible hydrolysis reaction mechanism was proposed : At pH $1.0{\sim}9.0$, not relevant to the hydrogen ion concentration, neutral $H_2O$ molecule competitvely attacked on the double bond. By contraries, above pH 9.0, it was proportional to concentration of hydroxide ion.

Indole Derivatives II. The Kinetics and Mechanism of the Hydrolysis of Indolylacrylophenone Derivatives (인돌 유도체 II. Indolylacrylophenone 유도체의 가수분해 반응에 대한 메카니즘과 그 반응 속도론적 연구)

  • Lee, Ki-Chang;Ryu, Jung-Wook
    • Journal of the Korean Applied Science and Technology
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    • v.9 no.2
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    • pp.119-126
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    • 1992
  • The kinetics of the hydrolysis of indolylacrylophenone derivatives(IA) was investigated by ultraviolet spectrophotometry in 30% dioxane-$H_2O$ at 25$^{\circ}C$ Rate equations were obtained over a wide pH range. On the basis of rate equation, general base catalysis and Hammett's plot, the mechanism of hydrolysis to the (IA) were proposed: Below pH 3.0, the hydrolysis of (IA) was proportional to hydronium ion concentration, between pH 4.0${\sim}$9.0 neutral water molecule and hydroxide ion were added to carbon-carbon double bond and over pH 10.0 hydrolysis of (IA) was proportional to hydroxide ion concentration.

Synthesis of Durable Softner for Cotton Fabrics and Its Characterization (면직물용 내구성유연제의 합성과 그의 특성화)

  • Lee, Ki-Chang;Park, Hong-Soo
    • Journal of the Korean Applied Science and Technology
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    • v.7 no.1
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    • pp.87-91
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    • 1990
  • 1,3-Di(2-octadecanoyl)-2,7-dioxy-l,3,6,8-tetra aza cyclodecane [DDTC] was synthesized by reacting octadecanoic acid, 2,2'-di-aminodiethyl amine with urea. O/W type softner (STA) was prepared by blending DDTC and pentaerithritol monostearate with polyoxysthylene (20) oleyl ether, polyoxyethylene (10) castor oil, and PEG #1000-lauric acid ester. Treating STA to all cotton fabrics, the physical properties, such as tear strength, crease recovery, flexing abrasion resistance, and so on were measured. Resulting the measurements, STA was found to be durable softner with softness.

Analysis of loop impedance characteristic based on korea internal electrical environment (국내환경을 고려한 loop impedance 특성 분석)

  • Jung, Jin-Soo;Han, Woon-Ki;Kim, O-Huan;Ahn, Jae-Min;Lee, Seung-Jae
    • Proceedings of the KIEE Conference
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    • 2009.07a
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    • pp.2174_2175
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    • 2009
  • This Paper present about loop impedance characteristic based on korea internal electrical environment. Analysis parameters were touch voltage, electrical shock current and human body resistance. Result, For protect of electrical shock must measuring of loop impedance. And current capacity & loop impedance are must important parameters.

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Synthesis of 4,6-Dichloro-3-[(1-N-Arylaminocarbonyl)-Hydrazono]- 1,3-Dihydro-Indole-2-One as a Potential NMDA Receptor Glycine Site Antagonist

  • Hwang, Ki-Jun;Lee, Tae-Suk
    • Archives of Pharmacal Research
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    • v.23 no.2
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    • pp.112-115
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    • 2000
  • A synthetic procedure for the preparation of indole-2,3-dione derivatives 6 as a potential NMDA receptor glycine site antagonist with improved pharmacological profile compared with 2-carboxyindole derivative 5, starting from readily available 3,5-dichloroaniline (7), is described.

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Benzoic acid II. The Kinetics and Mechanism of the Hydrolysis to 2-Furyl Chalcone Derivatives (벤조산 유도체 II. Furyl Chalcone 유도체의 가수분해 반응메카니즘과 그 반응속도론적 연구)

  • Lee, Ki-Chang;Hwang, Yong-Hyun;Ryu, Wan-Ho;Yang, Cheon-Hoi;Lee, Seok-Woo
    • Journal of the Korean Applied Science and Technology
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    • v.10 no.1
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    • pp.75-81
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    • 1993
  • The hydrolysis kinetics of 2-furyl chalcone derivatives $[I]{\sim}[V]$ was investigated by ultraviolet spectrophotometery in 30% dioxane-$H_{2}O$ at $25^{\circ}C$ and the structure of these compounds were ascertained by means of ultraviolet, infrared and NMR spectra. The rate equations which were applied over a wide pH range(pH $1.0{\sim}12.0$) were obtained. The substituent effects on 2-furyl chalcone derivatives $[I]{\sim}[V]$ were studied, and the hydrolysis were facilitated by the electron attrecting groups. On the basis of the rate equation, substituent effect, general base effect and final product. the plausible hydrolysis mechaism was proposed: Below pH 4.0, it was only proportional to concentration of hydronium ion, at pH $4.0{\sim}9.0$, neutral $H_{2}O$ molecule competitively attacked on the double bond. By contrast, above pH 9.0, it was proportional to concentration of hydroxide ion.