Studies on the optimal conditions for synthesizing poly(butylene succinate‐co‐terephthalate) copolyesters with targeted properties

Abstract

The aliphatic-aromatic copolyesters are becoming more important due to their desirable mechanical properties and biodegradability. In this study, a series of Poly(butylene succinate-co-terephthalate) (PBST) of various monomer compositions were synthesized from succinic acid (SA), dimethyl terephthalate (DMT), and 1,4-butanediol (BDO) in the presence of tetrabutyl titanate (Ti(Obu) 4 ). The experiment was divided into three parts. The first part is a 2 3 factorial design with permutations of three factors, namely, temperature, molar ratio of BDO/DMT, and molar ratio of SA/ DMT in polycondensation. Our statistical analysis showed that the temperature has a more significant effect on the intrinsic viscosity ([Z]) of PBST than the other two factors. The number-average molecular weight (M n ) of the PBST was determined from the intrinsic viscosity by using the Berkowitz model of M n = 1.521 Â 10 5 [Z] 1.5 . The second part of the experiment is a time course investigation of polycondensation under various temperatures, molar ratios of BDO/ (DMT + SA), and concentrations of Ti(Obu) 4 . Our results showed the best polycondensation occurred at 1.5 hr with [Z] reaching 0.49 dL/g when the temperature was held at 250 C, BDO/(SA + DMT) = 1.2 mol/mol with SA/(SA + DMT) = 50 mol%, and 0.97 mmol of Ti(Obu) 4 per mol of SA + DMT. The third part of the experiment involves searching for the best molar ratio of SA/(SA + DMT) in obtaining desirable polymer properties and biodegradability. The results showed that the highest melting point of PBST can be as high as 177 C at SA/(SA + DMT) = 30 mol%. The maximum tensile strength of 25.6 MPa is obtained at SA/(SA + DMT) = 30 mol%. The maximum elongation at break of 269.3% and the maximum Young's modulus of 754.8 MPa are reached at SA/(SA + DMT) = 60 mol% and at SA/(SA + DMT) = 30 mol%, respectively. The fastest lipase-decomposition rate of PBST reached 100 % at day six for samples with molar ratio SA/(SA + DMT) = 80 mol%.

The establishment and biological assessment of a whole tissue‐engineered intervertebral disc with PBST fibers and a chitosan hydrogel in vitro and in vivo

“…The compression strength and tensile strength of PBST fibers can reach up to 245 MPa and 418 MPa, respectively. Additionally, the tensile modulus of PBST fibers can reach up to 754 MPa . The tensile strength of PBST fibers can reach 418.2 MPa, and the elastic recovery can reach 95% .…”

“…Additionally, the tensile modulus of PBST fibers can reach up to 754 MPa. 29,30 The tensile strength of PBST fibers can reach 418.2 MPa, and the elastic recovery can reach 95%. 29 Compared with PBST, other common AF scaffold materials have poor mechanical properties.…”

Highly Stretchable Biobased Poly(butylene succinate)-Based Copolyesters with Shape Memory and Self-Healing Properties

“…[24][25][26][27] Poly(butylene succinate-co-terephthalate) (PBST) [28][29][30] is one such copolymer that has good biodegradability, high flexibility, and high toughness, [31][32][33] whose synthesis process, crystal structure, as well as thermomechanical and biodegradation characteristics have been studied extensively. [31][32][33][34][35] Zheng et al [36] synthesized a PBST copolymer with 50 mol% PBS and found that the crystalline abilities of both the PBS and PBT segments were limited; further, the melting point of the copolymer was 132 °C, and the elongation at break was enhanced to around 1300%. Shi and coworkers [37] reported a PBST copolymer with 35 mol% PBT that exhibited outstanding shape memory properties under different kinds of deformation; moreover, the reversion ratio of the sample was maintained above 97% even after 35 cycle times.…”