TY - JOUR
T1 - Natural Polymers from Biomass Resources as Feedstocks for Thermoplastic Materials
AU - Müller, Kerstin
AU - Zollfrank, Cordt
AU - Schmid, Markus
N1 - Publisher Copyright:
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/5
Y1 - 2019/5
N2 - With the objective of a more sustainable circular economy, one long-term goal is the utilization of renewable resources as feedstock for the production of polymer-based materials. In order to successfully process such materials using existing industrial-scale technologies or even recycling processes, the natural polymers must have thermoplastic properties. With only a few exceptions, natural polymers are not thermoplastic. However, chemical and physical modification techniques are able to induce thermoplasticity in natural polymers from biomass resources such as cellulose, lignin, and chitin. Modification techniques focus on masking the hydroxyl groups to disrupt dense hydrogen bonding and so enable polymer chain mobility upon heating. The introduction of long alkyl chains into the polymer backbone effectively improves the thermoplastic processing of natural polymers. With regard to polymer blending, chemical grafting and graft copolymerization are powerful tools for enhancing compatibility. For both chemical and physical modification, solvents such as ionic liquids and deep eutectic solvents are currently being explored for biomass and fiber processing and show promise for the future development of thermoplastic biopolymers. This review describes possible modifications, potential processing difficulties, and gives a summary of relevant studies described in the scientific literature.
AB - With the objective of a more sustainable circular economy, one long-term goal is the utilization of renewable resources as feedstock for the production of polymer-based materials. In order to successfully process such materials using existing industrial-scale technologies or even recycling processes, the natural polymers must have thermoplastic properties. With only a few exceptions, natural polymers are not thermoplastic. However, chemical and physical modification techniques are able to induce thermoplasticity in natural polymers from biomass resources such as cellulose, lignin, and chitin. Modification techniques focus on masking the hydroxyl groups to disrupt dense hydrogen bonding and so enable polymer chain mobility upon heating. The introduction of long alkyl chains into the polymer backbone effectively improves the thermoplastic processing of natural polymers. With regard to polymer blending, chemical grafting and graft copolymerization are powerful tools for enhancing compatibility. For both chemical and physical modification, solvents such as ionic liquids and deep eutectic solvents are currently being explored for biomass and fiber processing and show promise for the future development of thermoplastic biopolymers. This review describes possible modifications, potential processing difficulties, and gives a summary of relevant studies described in the scientific literature.
KW - cellulose
KW - chitin
KW - lignin
KW - plasticizers
KW - thermoplastic biopolymers
UR - http://www.scopus.com/inward/record.url?scp=85061811746&partnerID=8YFLogxK
U2 - 10.1002/mame.201800760
DO - 10.1002/mame.201800760
M3 - Review article
AN - SCOPUS:85061811746
SN - 1438-7492
VL - 304
JO - Macromolecular Materials and Engineering
JF - Macromolecular Materials and Engineering
IS - 5
M1 - 1800760
ER -