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A Faster Approach to Stereocomplex Formation of High Molecular Weight Polylactide Using Supercritical Dimethyl Ether

Authors
Bibi, GulnazJung, YoungmeeLim, Jong ChooKim, Soo Hyun
Issue Date
5월-2015
Publisher
POLYMER SOC KOREA
Keywords
fast stereocomplex; dimethyl ether; high molecular weight polylactides; supercritical fluid technology
Citation
POLYMER-KOREA, v.39, no.3, pp.453 - 460
Indexed
SCIE
SCOPUS
KCI
Journal Title
POLYMER-KOREA
Volume
39
Number
3
Start Page
453
End Page
460
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/93638
DOI
10.7317/pk.2015.39.3.453
ISSN
0379-153X
Abstract
Engineering the polylactide via stereocomplexation with supercritical fluid (SCF) technology paved way to fabricate polymers with enhanced thermal and mechanical properties. We aimed to establish a SCF medium with excellent solubility for PLA without any additional solvent/co-solvent. We, therefore, employed supercritical dimethyl ether to synthesize 100% stereocomplex polylactide from high molecular weight homopolymers with an excellent yield. The remarkable solubility of the homopolymers in dimethyl ether is the key for quick conversion to s-PLA. This study proves a rapid synthesis route of dry s-PLA powder with sc-DME at 250 bar, 70 degrees C and 1.5 h, which are reasonably achievable processing parameters compared to the conventional methods. The degree of stereocomplexation was evaluated under the effect of pressures, temperatures, times, homopolymer-concentrations and molecular weights. An increment in the degree of stereocomplexation was observed with increased temperature and pressure. Complete conversion to s-PLA was obtained for PLLA and PDLA with M-n similar to 200 kg.mol(-1) with a total homopolymer to total DME ratio of 6:100% w/w at prescribed reaction conditions. The degree of stereocomplexation was determined by DSC and confirmed by XRD. Considerable improvement in thermo-mechanical properties of s-PLA was observed. DSC and TGA analyses proved a 50 degrees C enhancement in melting transition and a high onset temperature for thermal degradation of s-PLA respectively.
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