• 제목/요약/키워드: 산 무수물

검색결과 59건 처리시간 0.029초

Synthesis and Properties of Photocurable Epoxy Modified Acrylates Using Half-Ester Acrylates (하프-에스터 아크릴레이트를 이용한 광경화형 에폭시 변성 아크렐레이트의 합성과 물성)

  • 김동국;임진규;김우근;허정림
    • Polymer(Korea)
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    • 제28권6호
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    • pp.531-537
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    • 2004
  • Various half-ester acrylates were prepared from anhydrides and 2-hydroxyethyl acrylate. Photocurable epoxy modified acrylates were prepared from synthesized half-ester acrylate and neopentylglycol diglycidylether. Physical properties such as hardness, yellowing, tensile strength and elongation were tested and compared as the structure of oligomer in cured-film differs. It was found that viscosity of neopentylglycol diglycidylether-hexahydrophthalic anhydride (NP-HA) was highest. Hardness and tensile strength of photocrosslinked neopentylglycol diglycidylether-hexahydrophthalic anhydride were better than those of other photocrosslinted epoxy acrylates. And 5% weight loss temperature of photocrosslinked neopentylglycol diglycidylether-hexahydrophthalic anhydride was higher than those of other photocrosslinked epoxy acrylates. Value of yellow index of photocrosslinked neopentylglycol diglycidyl ether-succinic anhydride (NP-SA) was lower than the other products.

Synthesis and Physical Properties of Biocompatible and Biodegradable Chitin Derivatives III. -Synthesis and Solubility of Ester Chitin Derivatives- (생체적합성과 생분해성을 갖는 키틴유도체의 합성 및 물성 III -에스테르 키틴 유도체의 합성과 용해 특성-)

  • Kim, Seon-Jeong;Lee, Young-Moo;Sung, Yong-Kiel;Kang, Inn-Kyu;Park, Young-Hoon
    • Applied Chemistry for Engineering
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    • 제4권4호
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    • pp.785-790
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    • 1993
  • Three ester-type chitin derivatives were synthesized by reacting chitin with acetic anhydride, propionic anhydride and n-butyric anhydride to form acetyl chitin(AC), propionyl chitin(PC) and n-butyryl chitin(BC). Methanesulfonic acid was used as a catalyst. FT-IR spectra and solid state CP/MAS $^{13}C-NMR$ spectra of three chitin derivatives showed that the substituents were mainly incorporated in the $C_6$ position of chitin. The ester-type chititn derivatives were dissolved well in formic acid and swollen in aqueous acidic solution.

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Effects os Stoichiometric Ratio on Dynamic Mechanical Behavior for an Epoxy/Anhydride System (에폭시/산무수물계에서 동역학적 거동에 미치는 화학양론비의 효과)

  • Kim, Deuk-Su;Lee, Jong-Geun
    • Korean Journal of Materials Research
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    • 제7권12호
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    • pp.1089-1096
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    • 1997
  • 본 연구에서는 에폭시/산무수물계에 화학양론비(r=산무수물/에폭시)를 0.5, 0.7,0.9,1.1로 변화시켜 서로 다른 두종류의 경화촉진제 1-cyanoethy1-2-ethy1-4-methy1 imidazole(2E4MZ-CN)과 N,N-dimethy1 benzy1 amine(BDMZ)을 첨가한 시료에 대한 경화거동과 경화 후 물성을 관찰하였다. 이 시료의 등온 경화거동은 동역학 측정기(dynamic mechanical analyzer, DMA)와 시차주사 열량분석기(differential scanning calorimeter, DSC)를 이용하여 조사하였다. DMA로부터 구해진 결과를 보면 경화시 상대저장강성을 (relative storage rigidity, RSR)과 상대손실강성율(relative loss rigidity, RSR)과 상대손실강성율(relative loss rigidity, RLR)의 변화가 r값과 경화촉진제의 종류에 영향을 받았다. 그리고 DSC결과는 r값이 감소함에 따라 경화가 촉진되는 것으로 나타났다. 경화물의 성질을 조사하기 위하여 사용된 DMA로부터 얻어진 유리전이온도(glass transition temperature, T$_{g}$)와 가교결합간의 평균분자량(average molecular weigh between crosslinks, M$_{c}$은 사용한 두 경화촉진제에 대하여 r값의 영향이 다르게 나타났다. BDMA의 경우는 T$_{g}$가 1:1화학양론비인 r=0.9에서 최고치를 보였으나, 2E4MZ-CN은 r이 감소함에 따라 계속 증가하는 양상을 보였다. 이와 같은 경향은 2E4MZ-CN을 경화촉진제로 사용하였을 때 에폭시가 과량으로 될수록 잔류 에폭시기들간의 에케르반응이 추가적으로 일어나 M$_{c}$가 감소하기 때문이다.

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Cure Kinetics for the Acid Anhydride-cured Epoxy System Using a Near-infrared Reflection Spectroscopy (근적외선 분광분석을 통한 산무수물경화 에폭시 시스템의 경화 동력학)

  • 곽근호;박수진;이재락
    • Polymer(Korea)
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    • 제24권1호
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    • pp.65-71
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    • 2000
  • The latent properties and cure kinetics of an acid anhydride-cured epoxy resin have been investigated by a near-infrared (NIR) reflection spectroscopy. The assignments of the latent properties and cure behaviors were performed by the measurements of the NIR reflectance for epoxide and hydroxyl groups at different temperatures. A comprehensive analysis of the origin, location, and shifts during reaction of all major NIR absorption peaks in the spectral range from 4000 to 7100 $cm^{-1}$ / was provided. The extent of reaction was determined from NIR absorption band at the 4530 $cm^{-1}$ / depending on epoxide concentration and cure temperature.

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Synthesis and Antibacterial Activity of Some Oxazolone Derivatives (옥사졸론 유도체의 합성과 항균성)

  • Aaglawe M. J.;S. S. Dhule;S. S. Bahekar;P. S. Wakte;D. B. Shinde
    • Journal of the Korean Chemical Society
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    • 제47권2호
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    • pp.133-136
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    • 2003
  • A series of oxazolone derivatives (4a-n) have been synthesized as a potential antibacterial agent. Titled compounds have been prepared by the condensation of aryloxy acetyl-amino-acetic acid with aldehyde in presence of ethanol, acetic anhydride and sodium acetate. The structures of the new compounds were established on the basis of $^1H$ NMR and IR spectral data.

Effect of External and Intramolecular Nucleophiles on Nature of Products of Carboxypeptidase A-Catalyzed Hydrolysis of Esters. Attempted Trapping of Acyl-Enzyme Intermediate (카르복시펩티다제A의 에스테르 가수분해 반응생성물의 종류에 대한 외부 및 분자내 친핵체의 영향. 아실-효소중간체의 포획시도)

  • Junghun Suh;Emil Thomas Kaiser
    • Journal of the Korean Chemical Society
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    • 제22권3호
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    • pp.164-172
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    • 1978
  • Carboxypeptidase A-catalyzed hydrolysis of ester substrates was carried out at room temperature in the presence of a number of external reagents. If the acyl-enzyme intermediate, an anhydride, is attacked by the external reagents, products formed by trapping at the acyl portion or at the enzyme portion of the anhydride group can be obtained. Examination of the uv/vis spectral properties of the reaction products and of changes in enzyme activity indicated that such trapping reactions did not occur. Also performed was evaluation of enzymatic rate parameters for the the hydrolysis of O-(o-hydroxyphenylacetyl)-L-${\beta}$-phenyllactate. Detection of 2-coumaranone possibly formed by attack of the o-hydroxy group as an intramolecular trapping group at the acyl-enzyme intermediate was tried, but no evidences for the intramolecular trapping reaction were obtained. Failure to trap the intermediate was discussed in terms of steric hindrance imposed on the approach of the trapping reagents to the anhydride group of the acyl-enzyme intermediate and of the fast enzymatic breakdown of the intermediate.

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Cure Behavior of an Epoxy/Anhydride System by Torsion Pendulum (Torsion Pendulum에 의한 에폭시/산무수물계의 경화거동)

  • Lee, Jong-Geun;Park, Won-Ho
    • Korean Journal of Materials Research
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    • 제6권5호
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    • pp.494-503
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    • 1996
  • 에폭시/산무수물계의 등온 경화거동을 새로이 제작된 Torsion Pendulum(TP)으로 다양한 온도에서 조사하였으며 경화반응을 촉진시키기 위하여 두 종류의 경화촉진제를 사용하였다. 새로이 제작된 TP는 개인용 컴퓨터를 이용하여 모든 기계\ulcorner인 작동과 date 수집 및 분석이 자동으로 처리될 수 있도록 하였다. 이 기기로부터 얻어진 결과인 경화 동안의 상대전단강성율(RSR, relative shear rigidity)과 log decrement(LD)의 변화로부터 제작된 TP가 잘 작동한다는 것을 알 수 있었다. 두 종류의 촉진제가 전체적인 경화과정에 미치는 촉진효과는 비슷하였으나 각 촉진제로부터 얻어진 LD 곡선을 보면 서로 다른 모양을 나타내었다. 이것은 경화촉진제가 반응 촉진효과 이외에도 경화거동에 영향을 미친다는 것을 의미하며, 따라서 이러한 경화거동의 차이는 경화물의 성질에 영향을 줄 수 있다.

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