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Efficient Depolymerization of Poly(ethylene 2,5-furanoate) Using Polyester Hydrolases.
Kumar, Virender; Pellis, Alessandro; Wimmer, Reinhard; Popok, Vladimir; Christiansen, Jesper de Claville; Varrone, Cristiano.
Afiliación
  • Kumar V; Department of Chemistry and Bioscience, Aalborg University, Fredrik Bajers Vej 7H, 9220 Aalborg, Denmark.
  • Pellis A; Dipartimento di Chimica e Chimica Industriale, Universitá degli Studi di Genova, Via Dodecaneso 31, Genova 16146, Italy.
  • Wimmer R; Department of Chemistry and Bioscience, Aalborg University, Fredrik Bajers Vej 7H, 9220 Aalborg, Denmark.
  • Popok V; Department of Materials and Production, Aalborg University, Fibigerstræde 16, 9220 Aalborg, Denmark.
  • Christiansen JC; Department of Materials and Production, Aalborg University, Fibigerstræde 16, 9220 Aalborg, Denmark.
  • Varrone C; Department of Chemistry and Bioscience, Aalborg University, Fredrik Bajers Vej 7H, 9220 Aalborg, Denmark.
ACS Sustain Chem Eng ; 12(26): 9658-9668, 2024 Jul 01.
Article en En | MEDLINE | ID: mdl-38966237
ABSTRACT
Poly(ethylene 2,5-furanoate) (PEF) is considered to be the next-generation green polyester and is hailed as a rising star among novel plastics. It is biobased, is nontoxic, and has comparable or improved properties compared to polyethylene terephthalate (PET). Biobased PEF offers lower life-cycle greenhouse gas emissions than PET. However, with its industrial production starting soon, relatively little is known about its actual recyclability. This work reports on the near complete depolymerization of PEF using two efficient PET hydrolases, FastPETase and leaf compost-cutinase (LCC), at loadings 4.5-17 times lower than previously reported. FastPETase and LCC exhibited maximum depolymerization of PEF, measured by weight loss and 2,5-furandicarboxylic acid (FDCA) production, using potassium phosphate-NaOH buffer at 50 and 65 °C, respectively. The 98% depolymerization of 13 g L-1 PEF film was achieved by three additions of the LCC in 72 h, while 78% weight loss was obtained using FastPETase in controlled conditions. Nonetheless, 92% weight loss was obtained with FastPETase when using only 6 g L-1 PEF. The main reaction products were identified as FDCA, ethylene glycol, and mono(2-hydroxyethyl)-furanoate. LCC performed better than FastPETase, in terms of both FDCA release and weight loss. The effect of crystallinity was evident on the enzymes' performance, as only 4% to 7% weight loss of crystalline PEF (32%) was recorded. Microscopy studies of the treated PEF films provided information on the surface erosion processes and revealed higher resistance of the crystalline phase, explaining the low level of depolymerization. The study presents important insights into the enzymatic hydrolysis of biobased PEF material and paves the path toward more viable applications within biopolymer waste recycling.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: ACS Sustain Chem Eng Año: 2024 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: ACS Sustain Chem Eng Año: 2024 Tipo del documento: Article País de afiliación: Dinamarca