TY - JOUR
T1 - Evaluation of Relationship Between Crystallization Structure and Thermal-Mechanical Performance of PLA with MCC Addition
AU - Wen, Huiying
AU - Wang, Yali
AU - Wang, Di
AU - de Claville Christiansen, Jesper
AU - Yu, Donghong
AU - Jiang, Shichun
AU - Chen, Chunxia
PY - 2019/9/13
Y1 - 2019/9/13
N2 - Poly(lactic acid) (PLA) biocomposite with 1 wt % microcrystalline cellulose (MCC) addition were prepared by melt-mixed method using torque rheometer and annealed under different isothermal conditions. The morphology, crystallization behaviors, thermal and dynamic-mechanical properties were evaluated by techniques of polarized optical microscopy (POM), differential scanning calorimetry (DSC), X-ray diffraction (XRD) and dynamic mechanical analysis (DMA). Nucleus density, crystallization rate and crystallinity (X
c) of PLA matrix were significantly increased by addition of MCC. It was found that MCC could improve the activity of PLA segments at low crystallization temperature (T
c), and the stability of segments in crystal lattice was also enhanced at high T
c. DSC and XRD analysis supported that MCC contributed to the transformation of α’ form into α form in PLA during annealing. The temperature range in which α crystal form appeared for pure PLA was 125 to 135 °C and it was enlarged from 105 to 145 °C for PLA with MCC addition. The Avrami exponent (n) and crystallization rate constant (k) for MCC/PLA decreased and increased respectively, supporting that the time dimension in nucleation mode was inhibited and crystallization kinetics was improved. MCC/PLA showed an increased stiffness and the highest value of storage modulus (E’) was 52 GPa at T
c of 125 °C, which is basically consistent with the condition of maximum X
c. DMA analysis supported that at high T
c, the addition of MCC greatly increased the crystallization ability of PLA and the elasticity and toughness were also improved.
AB - Poly(lactic acid) (PLA) biocomposite with 1 wt % microcrystalline cellulose (MCC) addition were prepared by melt-mixed method using torque rheometer and annealed under different isothermal conditions. The morphology, crystallization behaviors, thermal and dynamic-mechanical properties were evaluated by techniques of polarized optical microscopy (POM), differential scanning calorimetry (DSC), X-ray diffraction (XRD) and dynamic mechanical analysis (DMA). Nucleus density, crystallization rate and crystallinity (X
c) of PLA matrix were significantly increased by addition of MCC. It was found that MCC could improve the activity of PLA segments at low crystallization temperature (T
c), and the stability of segments in crystal lattice was also enhanced at high T
c. DSC and XRD analysis supported that MCC contributed to the transformation of α’ form into α form in PLA during annealing. The temperature range in which α crystal form appeared for pure PLA was 125 to 135 °C and it was enlarged from 105 to 145 °C for PLA with MCC addition. The Avrami exponent (n) and crystallization rate constant (k) for MCC/PLA decreased and increased respectively, supporting that the time dimension in nucleation mode was inhibited and crystallization kinetics was improved. MCC/PLA showed an increased stiffness and the highest value of storage modulus (E’) was 52 GPa at T
c of 125 °C, which is basically consistent with the condition of maximum X
c. DMA analysis supported that at high T
c, the addition of MCC greatly increased the crystallization ability of PLA and the elasticity and toughness were also improved.
KW - crystal form
KW - crystallinity
KW - crystallization dynamics
KW - dynamic-mechanical performance
UR - http://www.scopus.com/inward/record.url?scp=85073194902&partnerID=8YFLogxK
U2 - 10.1002/slct.201902015
DO - 10.1002/slct.201902015
M3 - Journal article
SN - 2365-6549
VL - 4
SP - 10174
EP - 10180
JO - ChemistrySelect
JF - ChemistrySelect
IS - 34
ER -