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Pushing Poly(Limonene Carbonate) Toward Commercial Applications: Bio‐Based Poly(Menth‐1‐Ene Carbonate)‐Graft‐Poly(n‐Butyl Acrylate) With Tailored Graft Density

DOI zum Zitieren der Version auf EPub Bayreuth: https://doi.org/10.15495/EPub_UBT_00009007
URN to cite this document: urn:nbn:de:bvb:703-epub-9007-4

Title data

Höferth, Marcel ; Schmalz, Holger ; Greiner, Andreas:
Pushing Poly(Limonene Carbonate) Toward Commercial Applications: Bio‐Based Poly(Menth‐1‐Ene Carbonate)‐Graft‐Poly(n‐Butyl Acrylate) With Tailored Graft Density.
In: European Journal of Lipid Science and Technology. Vol. 127 (2025) Issue 7 . - e70037.
ISSN 1438-9312
DOI der Verlagsversion: https://doi.org/10.1002/ejlt.70037

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Project information

Project title:
Project's official title
Project's id
Block- und Pfropfcopolymere auf Basis von Polylimonencarbonat, einem biobasiertem Polycarbonat mit vielversprechenden Materialeigenschaften
438886960
Open Access Publizieren
No information

Project financing: Deutsche Forschungsgemeinschaft

Abstract

Poly(limonene carbonate) (PLimC) is a promising material in the search for bio-based alternatives to fossil-based plastics, such as poly(styrene) and bisphenol A-based polycarbonates. PLimC is made from orange waste-derived limonene oxide (LimO) and CO2. The brittle behavior of PLimC remains a challenge for industrial applications. A possible solution could be the introduction of low Tg polymer grafts. The terpolymerization of trans-LimO, trans-menth-1-ene oxide (Men1O), and CO2 was shown to yield a terpolymer that can be used as a platform for controlled functionalization and tailored graft copolymerization. To transform the terpolymer into a macroinitiator for atom transfer radical polymerization (ATRP), the PLimC double bonds were post-modified with hydroxyl groups via thiol-ene click reaction of 2-mercaptoethanol and subsequently esterified with 2-bromoisobutyryl bromide (BiB). n-Butyl acrylate (nBA) was chosen as a bio-based monomer for grafting-from copolymerization to introduce low Tg side chains that increase the ductility of the otherwise brittle PLimC. Matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) was used to show the narrow molecular weight distribution of the side chains. Non-wovens made from PMen1C-g-PnBA were produced via electrospinning. PMen1C-g-PnBA was added as a compatibilizer for blends of PLimC and poly(n-butyl acrylate) (PnBA) and as a toughening agent for PLimC. Practical Applications: PMen1C-g-PnBA shows tunable mechanical properties by variation of PnBA content and graft density. Poly(limonene carbonate)’s brittle nature could be compensated by addition of PMen1C-g-PnBA, therefore opening up many possible industrial applications for PLimC to replace common fossil-based plastics. Additionally, filter applications of PMen1C-g-PnBA as sustainable electrospun non-wovens are possible.

Further data

Item Type: Article in a journal
DDC Subjects: 500 Science > 540 Chemistry
Institutions of the University: Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Macromolecular Chemistry II > Chair Macromolecular Chemistry II - Univ.-Prof. Dr. Andreas Greiner
Profile Fields > Advanced Fields > Polymer and Colloid Science
Research Institutions > Affiliated Institutes > Bavarian Polymer Institute (BPI)
Faculties
Faculties > Faculty of Biology, Chemistry and Earth Sciences
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Macromolecular Chemistry II
Profile Fields
Profile Fields > Advanced Fields
Research Institutions
Research Institutions > Affiliated Institutes
Language: English
Originates at UBT: Yes
URN: urn:nbn:de:bvb:703-epub-9007-4
Date Deposited: 19 Mar 2026 14:19
Last Modified: 19 Mar 2026 14:20
URI: https://epub.uni-bayreuth.de/id/eprint/9007

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