Reduction of molar mass loss and enhancement of thermal and rheological properties of recycled poly(lactic acid) by using chain extenders obtained from RAFT chemistry

2020 ◽  
Vol 153 ◽  
pp. 104628
Author(s):  
Juan José Benvenuta-Tapia ◽  
Eduardo Vivaldo-Lima
Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2791
Author(s):  
Juan José Benvenuta-Tapia ◽  
Pascale Champagne ◽  
José Alfredo Tenorio-López ◽  
Eduardo Vivaldo-Lima ◽  
Ramiro Guerrero-Santos

The aim of this contribution is to assess the use poly(styrene-co-glycidyl methacrylate-b-styrene) copolymers synthesized by nitroxide mediated polymerization (NMP) as chain extenders in the recycling of poly(lactic acid) biopolyester. Concisely, the addition of such block copolymers during the melt processing of recycled poly(lactic acid) (rPLA) leads to important increases in the viscosity average molecular weight of modified polymeric materials. Molar masses increase from 31,000 g/mol for rPLA to 48,000 g mol−1 for the resulting rPLA/copolymer blends (bPLA). Fortuitously, this last value is nearly the same as the one for pristine PLA, which constitutes a first piece of evidence of the molar mass increase of the recycled biopolymer. Thermograms of chain extended rPLA show significant decreases in cold crystallization temperature and higher crystallinity degrees due to the chain extension process using NMP-synthesized copolymers. It was found that increasing epoxide content in the NMP-synthesized copolymers leads to increased degrees of crystallinity and lower cold crystallization temperatures. The rheological appraisal has shown that the addition of NMP synthesized copolymers markedly increases complex viscosity and elastic modulus of rPLA. Our results indicate that P(S-co-GMA)-b-S) copolymers act as efficient chain extenders of rPLA, likely due to the reaction between the epoxy groups present in P(S-co-GMA)-b-PS and the carboxyl acid groups present in rPLA. This reaction positively affects viscometric molar mass of PLA and its performance.


2021 ◽  
Vol 138 (29) ◽  
pp. 50686
Author(s):  
Krishnaa B. Venkatesan ◽  
Sonal S. Karkhanis ◽  
Laurent M. Matuana

2007 ◽  
Vol 249-250 (1) ◽  
pp. 529-534 ◽  
Author(s):  
Fengwei Xie ◽  
Tao Xue ◽  
Long Yu ◽  
Ling Chen ◽  
Xiaoxi Li ◽  
...  

2008 ◽  
Vol 62 (1) ◽  
pp. 91-98 ◽  
Author(s):  
Fathilah Ali ◽  
Young-Wook Chang ◽  
Shin Choon Kang ◽  
Joon Yong Yoon

2020 ◽  
pp. 096739112093135
Author(s):  
Mohammad Mahdi Salehi ◽  
Fatemeh Hakkak

The main objective of the present work was to study the role of carbon nanotube (CNT) on the microstructure development and physical, mechanical, and rheological properties of poly(lactic acid) (PLA)/natural rubber (NR)/CNT hybrid nanocomposites. The PLA/NR blend samples with constant blend ratio (90/10) were prepared by melt mixing in a laboratory internal mixer at a temperature of 190°C. The behavior of the PLA/NR blend was examined depending on the CNT content (0.5–6 wt%). The droplet size and droplet size distribution of the NR phase decreases with the increase in CNTs content. This could be explained in terms of compatibilizing effect of CNT and the changing of the viscosity ratio of the blend phases. The development of the microstructure and the physical properties of the blend were also investigated according to the CNT contents by measuring the linear viscoelasticity. The elongational behavior and mechanical properties of the blends were strongly dependent on the location of the CNT. The CNT worked as an efficient compatibilizer and also it worked as a reinforcing filler making the matrix more rigid.


2019 ◽  
pp. 203-225
Author(s):  
Lee Tin Sin ◽  
Bee Soo Tueen

2011 ◽  
Vol 311-313 ◽  
pp. 1741-1745
Author(s):  
Chao Guo ◽  
Xiao Bo Sheng ◽  
Cheng Lin Chu ◽  
Yin Sheng Dong

Poly (lactic acid) (PLA) scaffolds with different sizes are often fabricated for various requirements. A cellular automaton simulation was used to investigate the effect of the size on the degradation behaviors of porous PLA scaffolds. Four porous PLA scaffolds with 90% initial porosity and different sizes were established by a novel repeat unit method. Mass loss and the change in molecular weight during the degradation were simulated. The results indicate that mass loss is related to the size of the porous scaffold while molecular weight change is independent on the size. With the size of the porous scaffold increasing, the mass loss increases while the difference in mass loss between the scaffolds with different sizes decreases. All these changes can be attributed to the difference in the autocatalytic effect and corresponding oligomer diffusion ability of the porous scaffolds with different sizes.


Polymer Korea ◽  
2018 ◽  
Vol 42 (3) ◽  
pp. 394-399
Author(s):  
Jae O Park ◽  
Woo Jin Choi ◽  
Kwang Je Kim ◽  
Jae Heung Lee ◽  
Jae Sup Shin

Sign in / Sign up

Export Citation Format

Share Document