• Title/Summary/Keyword: DMT(Dimethylterephthalate)

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Studies on Synthesis of Liquid Polyester Polyol by using DMT(Dimethylterephthalate) and NDC(Dimethyl-2,6-Naphthalene Dicarboxylate) (DMT(Dimethylterephthalate), NDC(Dimethy1-2,6-Naphthalene Dicarboxylate)를 이용한 액상 폴리에스터 폴리올의 합성에 관한 연구)

  • Kim, Sang-Hern
    • Journal of the Korean Applied Science and Technology
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    • v.26 no.3
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    • pp.317-327
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    • 2009
  • In this study DMT(Dimethylterephthalate), NDC(Dimethyl-2, 6-Naphthalene Dicarboxylate) were used to synthesize polyester polyol which shows enhanced storage stability, improved flame retardancy, and good compressive strength. If DMT and NDC react respectively with DEG(Diethylene Glycol) which is kind of linear diol, the obtained polyester polyols tend to crystallize easily after the reaction. In case of DMT, PA(Phthalic Anhydride) which has asymmetric structure was introduced to retard the crystallization. In case of NDC, DPG(Dipropylene Glycol) which has an methyl side chain was introduced to prevent the crystallization. It was found that to introduce DPG was much more effective method to prevent the crystallization than PA. NDC and DMT were reacted together with DPG for various compositions of NDC:DMT(8:2, 6:4, 4:6 mol ratio). The obtained NDC-DMT-DPG based polyester polyol showed improved flame retardancy, and good compressive strength with increasing the content of NDC.

Synthesis and Characterization of Poly(1,4-cyclohexanedimethylene/ethylene terephthalate) (Poly(1,4-cyclohexanedimethylene/ethylene terephthalate)의 합성 및 물성)

  • Cho, In-Ho;Rhee, Jong M.;Lee, Jong-Shin
    • Textile Coloration and Finishing
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    • v.3 no.3
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    • pp.23-28
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    • 1991
  • Poly(1, 4-cyclohexanedimethylene/ethylene terephthalate), PCET was prepared by condensing 1, 4-cyclohexanedimethanol(CHDM) and ethylene glycol with dimethylterephthalate(DMT), and some thermal properties of PCET were studied by DSC at a heating rate $20^{\circ}C$min. On increasing the CHDM content in PCET up to 20 mole%/DMT, the glass transition temperature(Tg) decreased a little and the crystallizability reduced sharply, and from 20 to 50 mole %/DMT the $T_g$ did not changed and the crystallization temperature was not detected. But on increasing the CHDM content above 70 mole %/DMT the TEX>$T_g$/ and the melting temperature increased.

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The Kinetics of Transesterification between Dimethylterephthalate and 1,3-Propanediol (디메틸 테레프탈레이트와 1,3-프로판디올 사이의 에스테르교환반응에 관한 연구)

  • Na, Sang-Kuwon;Kong, Byeong-Gi;Choi, Chang-Yong;Kim, Jung-Gyu;Hong, Wan-Hae;Nah, Jae-Woon
    • Polymer(Korea)
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    • v.29 no.1
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    • pp.41-47
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    • 2005
  • The transesterification of dimethyl terephthalate (DMT) with 1,3-propanediol (PDO) was investigated in the presence of catalyst, titanium (IV) butoxide (TBO), at 175~190 $^{\circ}C$ . The degree of transesterification reaction was measured by the output of methanol which was distilled from the reactor. The amount of methanol increased as the reaction temperature, molar ratio and catalyst concentration increased. The observed overall rate of the transesterification was third order; first order with respect to DMT, PDO, and the concentration of catalyst, respectively. Using calculated rate constants, the activation energy for transesterification was 26.93 kcal/mole. The melting temperature of bis(2-hydroxytrimethyl) terephthalate (BHTMT) was 85.2$^{\circ}C$ and heat of fusion 141.3 J/g.

Transesterification of Dimethyl Terephthalate with Diethylene Glycol (Dimethyl terephthalate와 diethylene glycol의 에스테르 교환 반응)

  • Kim, Gunhyung;Cho, Minjeong;Jeon, Yeonghwan;Han, Myungwan;Kang, Kyungsuk
    • Korean Chemical Engineering Research
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    • v.53 no.2
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    • pp.253-261
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    • 2015
  • The kinetics of the transesterification of dimethyl terephthalate (DMT) with diethylene glycol (DEG) was studied in a batch reactor. bis-hydroxyethoxytethyl-terephthalate (BHEET), which is polyester polyol monomer, can be produced by the transesterification reaction. Zinc acetate was used as a catalyst. Previous kinetic studies was carried out in a semi-batch reactor where generated methanol was removed so that reverse reactions were not considered in the kinetic expressions, resulting in inaccuracy of the kinetic model. Mathematical models of a batch reactor for the tranesterification reaction, which took the reverse reaction into account, were developed and used to characterize the reaction kinetics and the composition distribution of the reaction products. More accurate models than previous ones were obtained and found to have a good agreement between model predictions and experimental data. Effect of process variables on the esterification reaction was investigated based on the experimental and simulation results.

Preparation of Elastic Branched Copolyester for Toner Binder: Effects of Branching Agents (토너 바인더용 분지화된 탄성 폴리에스테르 공중합체의 합성: 분지제의 영향)

  • Roh, Hyung-Jin;Lim, Jong-Kwan;Lee, Dong-Ho;Yoon, Keun-Byoung
    • Polymer(Korea)
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    • v.36 no.4
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    • pp.440-447
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    • 2012
  • The branched copolyester was synthesized and its molecular weight, $T_g$, 1/2 method temperature ($T_{1/2}$) and rheological properties were characterized for the application of toner binder. The linear copolyester had low molecular weight and melt elasticity obtained by dimethylterephthalate (DMT), ethylene glycol (EG) and 2,2-bis(4-(2-hydroxypropoxy) phenyl)propane (HPP). The branched copolyesters prepared with various branching agents such as 2-(hydroxymethyl)-2-ethylpropane-1,3-diol (trimethylol propane, TMP), 2,2-bi(hydroxymethyl)-1,3-propanediol (pentaerythritol, PER), 1,2,4-benzenetricarboxylic anhydride (trimellitic anhydride, TMA) and glycerol to improve the physical properties of the linear copolyester. The effect of branching agents on the molecular weight and melt elasticity of the branched copolyester was examined. The branched copolyesters prepared by adding over 15 mol% of branching agent showed relatively high molecular weight and melt elasticity, and $T_{1/2}$ value of $140^{\circ}C$. Therefore, the highly branched copolyesters were deemed suitable as a hot-melt toner of laser print process.