• Title/Summary/Keyword: 1,4-Cyclohexanedimethanol

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Conjugate Spun of Polyethylene Terephthalate Resin Modified with 1,4-Cyclohexanedimethanol

  • Bang, Ho-Ju;Kim, Hak-Yong;Jin, Fan-Long;Woo, Je-Wan;Park, Soo-Jin
    • Bulletin of the Korean Chemical Society
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    • v.32 no.2
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    • pp.541-546
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    • 2011
  • In this study, conjugate fibers were prepared from 1,4-cyclohexanedimethanol-modified polyethylene terephthalate (PET) resin using side by side conjugate spinning, sea-island type conjugate spinning, and split type conjugate spinning methods, and the properties of the conjugate fibers were investigated via several techniques. When viscosity increased, the tenacity of side by side conjugate fibers was increased, whereas elongation decreased. The sea-island conjugate fibers showed lower weight loss and surface color difference (K/S) values relative to that of regular PET fibers at the same conditions. The SEM results indicate that orange type spilt readily produced at a temperature range of 120 - 140$^{\circ}C$.

New Aliphatic Diol/Dicarboxylic Acid Based Biodegradable Polyesters and Their in-vitro Degradations (새로운 지방족 디올/디카복실산계 생분해성 폴리에스테르 및 가수분해 특성)

  • Kang Tae-Gon;Han Yang-Kyoo
    • Polymer(Korea)
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    • v.29 no.3
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    • pp.314-319
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    • 2005
  • Four kinds of new aliphatic diols were synthesized by the ring opening reaction of glycolide with 1,4-butanediol, 1,6-hexanediol, 1,4-cyclohexanediol, or 1,4-cyclohexanedimethanol, a difunctional initiator, in the presence of stannous octoate catalyst. The resulting diols were melt-polymerized with succinic acid, adipic acid, or suberic acid at 170, 190, or $220^{circ}C$ to produce new sequentially ordered aliphatic polyesters and their corresponding polyesters with random structure. Their glass transition temperatures ($T_g$) ranged from -40 to $30^{circ}C$, The sequentially ordered polyesters prepared at $170^{cir}C$ had higher $T_g$ of 5 to $10^{circ}$ than the polyesters with rand()m structure produced at higher temperature. From in-vitro degradation test the sequentially ordered polyesters was shower in the rate of hydrolysis in a buffer solution than the polymers with random molecular structure.

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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Endocrine Disruption Potentials of Bisphenol A Alternatives - Are Bisphenol A Alternatives Safe from Endocrine Disruption?

  • Ji, Kyunghee;Choi, Kyungho
    • Journal of Environmental Health Sciences
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    • v.39 no.1
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    • pp.1-18
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    • 2013
  • Objectives: Although a great body of knowledge is available on the toxicity of bisphenol A (BPA), little is known about that of BPA alternatives, such as bisphenol analogues (BPs) or $Tritan^{TM}$ copolyesters. This review provides a summary of the available information on the toxicity of BPs and three components of $Tritan^{TM}$, with a special focus on endocrine disruption. Methods: We collected from the literature a battery of in vitro and in vivo assay data developed to assess endocrine disruption of four BPs (bisphenol AF, B, F, and S) and three major components of $Tritan^{TM}$ ((di-methylterephthalate (DMT), 1,4-cyclohexanedimethanol (CHDM), and 2,2,4,4-tetramethyl-1,3-cyclobutanediol (TMCD)). Results: Several alternative compounds were identified as possessing comparable or even greater endocrinedisrupting effects than BPA in in vitro and in vivo studies. Conclusions: Potential endocrine disruption of BPA alternatives requires further studies on health consequences in experimental animals and in humans following longer term exposure.