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Thermal Behavior and Molecular Interaction of Poly(3-hydroxybutyrate-c o-3-hydroxyhexanoate) Studied by Wide-Angle X-ray Diffraction

The thermal behavior and molecular interaction of a new type of bacterial copolyester, poly(3-hydroxybutyrate-co-3-hydroxyhexanoate), P(HB-co-HHx) (HHx = 12 mol %), was investigated by using wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). The WAXD measurements were c...

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Published in:Macromolecules 2004-05, Vol.37 (10), p.3763-3769
Main Authors: Sato, Harumi, Nakamura, Masayuki, Padermshoke, Adchara, Yamaguchi, Hiroshi, Terauchi, Hikaru, Ekgasit, Sanong, Noda, Isao, Ozaki, Yukihiro
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cited_by cdi_FETCH-LOGICAL-a391t-af4535ca4b38f31423d4dd82fe9a3e41525f3a16d7944f919aa6c461389376c33
cites cdi_FETCH-LOGICAL-a391t-af4535ca4b38f31423d4dd82fe9a3e41525f3a16d7944f919aa6c461389376c33
container_end_page 3769
container_issue 10
container_start_page 3763
container_title Macromolecules
container_volume 37
creator Sato, Harumi
Nakamura, Masayuki
Padermshoke, Adchara
Yamaguchi, Hiroshi
Terauchi, Hikaru
Ekgasit, Sanong
Noda, Isao
Ozaki, Yukihiro
description The thermal behavior and molecular interaction of a new type of bacterial copolyester, poly(3-hydroxybutyrate-co-3-hydroxyhexanoate), P(HB-co-HHx) (HHx = 12 mol %), was investigated by using wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). The WAXD measurements were carried out over a temperature range from 25 to 110 °C in the scattering angle range of 2θ = 5−13°. The WAXD pattern at room temperature shows that the P(HB-co-HHx) copolymer has an orthorhombic system (α = β = γ = 90°) with a = 5.76 Å, b = 13.20 Å, and c = 5.96 Å (fiber repeat), which is identical to the crystal system of poly(3-hydroxybutyrate) (PHB) homopolymer. However, temperature-dependent variations in the lattice parameters, a and b, of P(HB-co-HHx) are quite different from those of PHB. Only the a lattice parameter increases with temperature, while the b lattice parameter changes very little in the case of crystalline P(HB-co-HHx). It seems that the intermolecular and intramolecular interactions between the CO group and the CH3 group decrease along the a axis of crystalline P(HB-co-HHx) with temperature. The (110) peak area of P(HB-co-HHx) starts decreasing from around 50 °C while that of PHB changes little at least until 140 °C, indicating that the crystallinity of PHB remains almost unchanged until 140 °C, but that of P(HB-co-HHx) decreases gradually from fairly low temperature (∼50 °C). The DSC measurement of the chloroform solution cast P(HB-co-HHx) shows a recrystallization peak around 51 °C. The (110) peak area of WAXD pattern of the chloroform solution cast P(HB-co-HHx) shows a maximum value at around 54 °C. The maximum of the (110) peak area demonstrates the recrystallization process of P(HB-co-HHx). The result is in a good agreement with the result of the DSC measurement.
doi_str_mv 10.1021/ma049863t
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The (110) peak area of P(HB-co-HHx) starts decreasing from around 50 °C while that of PHB changes little at least until 140 °C, indicating that the crystallinity of PHB remains almost unchanged until 140 °C, but that of P(HB-co-HHx) decreases gradually from fairly low temperature (∼50 °C). The DSC measurement of the chloroform solution cast P(HB-co-HHx) shows a recrystallization peak around 51 °C. The (110) peak area of WAXD pattern of the chloroform solution cast P(HB-co-HHx) shows a maximum value at around 54 °C. The maximum of the (110) peak area demonstrates the recrystallization process of P(HB-co-HHx). 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The (110) peak area of P(HB-co-HHx) starts decreasing from around 50 °C while that of PHB changes little at least until 140 °C, indicating that the crystallinity of PHB remains almost unchanged until 140 °C, but that of P(HB-co-HHx) decreases gradually from fairly low temperature (∼50 °C). The DSC measurement of the chloroform solution cast P(HB-co-HHx) shows a recrystallization peak around 51 °C. The (110) peak area of WAXD pattern of the chloroform solution cast P(HB-co-HHx) shows a maximum value at around 54 °C. The maximum of the (110) peak area demonstrates the recrystallization process of P(HB-co-HHx). 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The WAXD measurements were carried out over a temperature range from 25 to 110 °C in the scattering angle range of 2θ = 5−13°. The WAXD pattern at room temperature shows that the P(HB-co-HHx) copolymer has an orthorhombic system (α = β = γ = 90°) with a = 5.76 Å, b = 13.20 Å, and c = 5.96 Å (fiber repeat), which is identical to the crystal system of poly(3-hydroxybutyrate) (PHB) homopolymer. However, temperature-dependent variations in the lattice parameters, a and b, of P(HB-co-HHx) are quite different from those of PHB. Only the a lattice parameter increases with temperature, while the b lattice parameter changes very little in the case of crystalline P(HB-co-HHx). It seems that the intermolecular and intramolecular interactions between the CO group and the CH3 group decrease along the a axis of crystalline P(HB-co-HHx) with temperature. The (110) peak area of P(HB-co-HHx) starts decreasing from around 50 °C while that of PHB changes little at least until 140 °C, indicating that the crystallinity of PHB remains almost unchanged until 140 °C, but that of P(HB-co-HHx) decreases gradually from fairly low temperature (∼50 °C). The DSC measurement of the chloroform solution cast P(HB-co-HHx) shows a recrystallization peak around 51 °C. The (110) peak area of WAXD pattern of the chloroform solution cast P(HB-co-HHx) shows a maximum value at around 54 °C. The maximum of the (110) peak area demonstrates the recrystallization process of P(HB-co-HHx). The result is in a good agreement with the result of the DSC measurement.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma049863t</doi><tpages>7</tpages></addata></record>
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subjects Applied sciences
Exact sciences and technology
Organic polymers
Physicochemistry of polymers
Properties and characterization
Structure, morphology and analysis
title Thermal Behavior and Molecular Interaction of Poly(3-hydroxybutyrate-c o-3-hydroxyhexanoate) Studied by Wide-Angle X-ray Diffraction
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