• 제목/요약/키워드: Copolyesters

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음이온형 수분산성 공중합 폴리에스테르의 합성 및 응용 연구(I)

  • 엄성일;고석원
    • 한국섬유공학회:학술대회논문집
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    • 한국섬유공학회 1994년도 추계 학술발표회
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    • pp.135-136
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    • 1994
  • Anionic water dispersible copolyesters were synthesized by the polycon-densation of dimethyl isophathalate/5-sodium sulfo dimethyl isophathalate with ethylene glycol/diethylene glycol. Structrual analyses such as NMR, Irm WAXD analyses were done and copolyesters were found to be correctly synthesized. Relation between feed ratio and composition ratio of EG/DEG in copolyesters was confirmed by NMR analysis. Solubility test was done to find out optimum conditon of DMS feed ration of 10 mol% in dimethyl esters. Water resistance of copolyesters decreased with the increase of DMS or DEG molar feed ratio.

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Enzymatic and Non-enzymatic Degradation of Poly (3-Hydroxybutyrate-co-3-Hydroxyvalerate) Copolyesters Produced by Alcaligenes sp. MT-16

  • Choi Gang Guk;Kim Hyung Woo;Rhee Young Ha
    • Journal of Microbiology
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    • 제42권4호
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    • pp.346-352
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    • 2004
  • Poly(3-Hydroxybutyrate-co­3-Hydroxyvalerate), poly(3HB-co-3HV), copolyesters with a variety of 3HV contents (ranging from 17 to $60\;mol\%$) were produced by Alcaligenes sp. MT-16 grown on a medium containing glucose and levulinic acid in various ratios, and the effects of hydrophilicity and crystallinity on the degradability of the copolyesters were evaluated. Measurements of thermo-mechanical pro­perties and Fourier-transform infrared spectroscopy in the attenuated total reflectance revealed that the hydrophilicity and crystallinity of poly(3HB-co-3HV) copolyesters decreased as 3HV content in the copolyester increased. When the prepared copolyester film samples were non-enzymatically hydrolysed in 0.01 N NaOH solution, the weights of all samples were found to have undergone no changes over a period of 20 weeks. In contrast, the copolyester film samples were degraded by the action of extra­cellular polyhydroxybutyrate depolymerase from Emericellopsis minima W2. The overall rate of weight loss was higher in the films containing higher amounts of 3HV, suggesting that the enzymatic degra­dation of the copolyester is more dependent on the crystallinity of the copolyester than on its hydro­philicity. Our results suggest that the degradability characteristics of poly(3HB-co-3HV) copolyesters, as well as their thermo-mechanical properties, are greatly influenced by the 3HV content in the copoly­esters.

Biocompatibility of Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) Copolyesters Produced by Alcaligenes sp. MT-16

  • Choi, Gang-Guk;Kim, Hyung-Woo;Kim, Young-Baek;Rhee, Young-Ha
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제10권6호
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    • pp.540-545
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    • 2005
  • Poly(3-hydroxybutyrate-co-3-hydroxyvalerate), poly(3HB-co-3HV), copolyesters, with 3-hydroxyvalerate (3HV) contents ranging from 17 to 60 mol%, were produced by Alcaligenes sp. MT-16, and their biocompatibility evaluated by the growth of Chinese hamster ovary (CHO) cells and the adsorption of blood proteins and platelets onto their film surfaces. The number of CHO cells that adhered to and grew on these films was higher with increasing 3HV content. In contrast, the tendency for blood proteins and platelets to adhere to the copolyester surfaces significantly decreased with increasing 3HV content. Examination of the surface morphology using atomic force microscopy revealed that the surface roughness was an important factor in determining the biocompatibility of theses copolyesters. The results obtained in this study suggest that poly(3HB-co-3HV) copolyesters, with >30 mol% 3HV, may be useful in biocompatible biomedical applications.

Synthesis and Characterization of Copolyester Sizing Agents

  • Baik, Doo-Hyun;Kim, Gil-Lae
    • Fibers and Polymers
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    • 제2권1호
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    • pp.148-151
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    • 2001
  • The effect of main chain structure of anion-containing copolyesters on the properties of copolyester sizing agents was investigated. The copolyesters were prepared by conventional two step polymerization technique from DMT, DMI, DMS, EG, and DEG. The copolyesters synthesized were characterized by atomic absorption spectroscopy, $^1$H-NMR Spectroscopy, GC, FTIR Spectroscopy, and DSC. The solubility decreased as the DMT content increased. The copolyesters having DMT:DMI = 1:1 showed the minimum viscosity. The effect of EG content on the solution stability was not clear and the samples having high DMI content showed better solution stability. The water resistance was best when only DMI and EG were used, while it was worst when DMT:DMI was 1:0.

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음이온형 수분산성 공중합 폴리에스테르의 합성 및 응용 연구(II)

  • 엄성일;고석원
    • 한국섬유공학회:학술대회논문집
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    • 한국섬유공학회 1994년도 추계 학술발표회
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    • pp.137-138
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    • 1994
  • Anionic water dispersible copolyesters were synthesized and characterized. Viscosity of the copolyester is lower than that of routine acrylic water dispersible polymers. Adhesive force of the copolyester was much higher than that of water dispersible acrylic polymers. Particle size of the copolyesters in water decreased with the increase of DMS or DEG feed ratio. With the conclusive study of the data of particle size and potential, it was found that the dispersion stability of copolyesters in water increased with the increase of DMS or DEG feed ratio. Judging from the results of potential and particle size of copolyesters, there seems to be competition between two dispersion stability factors, i.e. electrostatic stabilization and steric stabilization and as a result, morphological change of particles occurrs. Tg decreased with the increase of DEG molar feed ratio or oil contents.

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락톤류로부터 Hydrogenophaga pseudoflava와 Ralstonia eutropha H16 두 세균에 의한 공중합 PHA의 합성 및 미세구조적 특성 연구 (Synthesis of Copolymeric PHA by Hydrogenophaga pseudoflava and Ralstonia eutropha H16 from Vari-ous Lactones and Their Microstructural Studies)

  • 장영옥;남원;최문환;송재준;윤성철
    • 한국미생물·생명공학회지
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    • 제28권2호
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    • pp.71-79
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    • 2000
  • Two typess of copolyesters, poly(3-hydroxybutyric acid-co-4-hydroxy-butyric acid)[P(3HB-co-4HB] and poly(3-hydroxybutyric acid-co-3-hydroxyvaleric acid)[P(3HB-co-3HV)], with various monomer ratios and different degree of microstructural heterogeneity were synthesized from Ralstonia eutropha H16 and Hydrogenophaga pseudoflava by using ${\gamma}$-butyrolactone and ${\gamma}$-valerolactone, respectively. The two bacteria showed a large difference in the utilization of ${\gamma}$-butyrolactone for cell growth and PHA synthesis. H. pseudoflava synthesized P(3HB-co-4HB) copolyesters with a wide range of 4HB content from 13 to 96 mol% depending on culture conditions, whiel R. eutropha H16 was able to synthesize the copolyesters containing less than 20 mol% of 4HB. An increase in the 4HB content in the P(3HB-co-4HB) copolyesters synthesized by H. pseud-oflava induced an lowering of their melting temperatures as well as their enthalpies of fusion. The increase in the 4HB content, however, increased the rate of degradation by an extracellular P(3HB) depolymerase. NMR spectros-copy and differential scanning calorimetry showed that the P(3HB-co-4HB) copolyesters from H. pseudoflava were generally microstructurally heterogeneous. The P(3HB-co-4HB) copolyesters) synthesized by R. eutropha H16 were rather random copolymers showing less microstructural heterogeneity than those synthesized by H. pseudoflava. The NMR D value analysis suggested that the monomer distribution of the P(3HB-co-3HV) copolymers from the two bacteria were relatively random.

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기능성 폴리에스테르 공중합체의 합성, PET와의 블렌드 및 카본 블랙 Dry Color의 물성 (Synthesis of Functional Copolyester, its Blend with PET, and Properties of Carbon Black Dry Color)

  • 박이순;이동찬;김진곤;허완수
    • 공업화학
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    • 제7권3호
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    • pp.496-503
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    • 1996
  • 고농도 안료 분산용 매스터 배취 제조를 위해 방향족 및 지방족형 폴리에스테르 공중합체들을 에스테르화 반응 및 중축합반응의 두 단계 반응으로 합성하였으며 이들을 안료 없이 PET에 블렌드하였을 때 열적성질과 유변학적 특성의 변화를 조사하였다. GPC 분석결과 합성된 폴리에스테르 공중합체는 $M_n{\approx}30000g/mol$, $M_w{\approx}65000g/mol$의 분자량을 가졌고, DSC 분석결과 $90{\sim}150^{\circ}C$$T_m$을 가졌으며 $^1H$-NMR 분석결과 공단량체 공급비와 공중합체내 조성비가 거의 일치하였다. 합성된 공중합체 중 $90{\sim}120^{\circ}C$$T_m$을 갖는 방향족, 지방족 폴리에스테르 공중합체, 그리고 표준시료인 SPA를 각각 PET와 용융 블렌드 하였으며 DSC 분석결과 상용성이 있음을 확인하였다. 그리고 이들의 전단속도 변화에 따른 용융점도의 변화를 조사하였는데 방향족 폴리에스테르 공중합체의 경우 PET내 폴리에스테르 공중합체의 함량이 증가할수록 용융점도가 증가하였으며, 지방족 폴리에스테르 공중합체와 표준시료 SPA의 경우는 이와 반대의 경향을 나타내었다. 카아본 블랙 dry color의 분산시간에 따른 체적저항은 방향족 폴리에스테르 공중합체가 가장 큰 값을 보였으며 이로부터 방향족 폴리에스테르 공중합체가 가장 적합한 분산제임을 알았다.

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Miscibility of Branched Polycarbonate Blends with Poly(ethylene-co-1,4-dimethyl cyclohexane terephthalate) Copolyesters

  • Song, Jeong-Oh;Jeon, Mi-Young;Kim, Chang-Keun
    • Macromolecular Research
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    • 제15권7호
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    • pp.640-645
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    • 2007
  • The phase behavior of branched polycarbonate (BPC) blends with poly(ethylene terephthalate-co-1,4-dimethyl cyclohexane terephthalate) copolyesters (PECT), as well as their rheological properties, were assessed. Even though BPC blends with PECT prepared by solvent casting proved to be immiscible, BPC and PECT copolyesters containing 1,4-dimethyl cyclohexane (CHDM) from 32 to 80 mole% formed homogeneous mixtures upon heating. The homogenization temperatures of the blends decreased with increasing CHDM content in PECT. The interaction energies of the BPC-PECT pairs calculated from the phase boundary in accordance with the lattice-fluid theory were positive and also decreased with increasing CHDM content in PECT. It was shown that the phase homogenization of these blends occurs upon heating when the combinatorial entropy term, which is favorable for miscibility, overcomes unfavorable energetic terms at elevated temperatures. A novel product, which is not limited by the drawbacks of linear polycarbonate (PC) and evidences processability superior to that of the PC/PECT blends, can be developed via the blending of BPC and PECT.

Synthesis and Crystallization Behaviors of Modified PET Copolymers

  • Hu, Seung-Woo;Myung, Hee-Soo;Bae, Jong-Seok;Yoo, Eui-Sang;Im, Seung-Soon
    • Fibers and Polymers
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    • 제1권2호
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    • pp.76-82
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    • 2000
  • A series of random copolyesters having various compositions were synthesized by bulk copolymerization of bishydroxyethyl terephthalate (BHET) with 1,4-cyclohexane dimethanol (CHDM) or dimethyl isophthalate (DMI). CHDM and DMI content was less than 10 wt%. For the synthesized copolyesters, isothermal crystallization rate, melting behavior, and equilibrium temperature were investigated by calorimetry and by Avrami and Hoffman-Weeks equation. Crystalline lattice and morphology were studied by WAXD and SEM. Regardless of the composition, the value of the Avrami exponent was about 3, which indicates that crystallization mechanism of the copolyester was similar to those of PET homopolymer. Incoporation of CHDM or DMI units in PET backbone decreased the crystallization rate of the copolyesters. Surface free energy of copolyesters was evaluated using the newly proposed equation. The value of surface free energy was about 189$\times$$10^{-6}$/$J^{2}$/$m^{4}$ regardless of comonomer contents. This result is in good agreement with that of PET homopolymer.

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Poly(butylene glutarate-co-adipate-co-succinate-co-terephthalate) 공중합체의 서열분포 및 열적성질 (Sequence Distribution and Thermal Property of Poly(butylene glutarate-co-adipate-co-succinate-co-terephthalate) Copolyesters)

  • 박상순;조윤;강혜정
    • 대한화학회지
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    • 제43권6호
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    • pp.682-690
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    • 1999
  • 사성분계 랜덤 공중합체인 poly(butylene glutarate-co-adipate-co-succinate-co-terephthalate)(PBGAST)를 합성하고 $^1H-NMR$ 분광분석법, 시차주사열량분석법(DSC) 및 X-선회절법 등을 시행하였다. PBGAST 공중합체의 융점거동과 결정화거동은 반응조건 뿐 만 아니라 공중합체내 terephthalate 단위의 함량에도 의존하였다.

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