The growing environmental awareness,the search for alternatives to fossil resources,and the goal of achieving a circular economy have all contributed to the increasing valorization of biowaste to produce bio-based pol...The growing environmental awareness,the search for alternatives to fossil resources,and the goal of achieving a circular economy have all contributed to the increasing valorization of biowaste to produce bio-based polymers and other high-value products.Among the various biowaste materials,lignin has gained significant attention due to its high aromatic carbon content,low cost,and abundance.Lignin is predominantly sourced as a byproduct from the paper industry,available in large quantities from hardwood and softwood,with variations in chemical structure and susceptibility to hydrolysis.This study focuses on softwood lignin obtained through the LignoForce^(TM) technology,comparing the thermal and chemical characteristics,and stability,of a recently produced batch with that of a batch that has been stored for four years.Additionally,the development of lignin-based thermoplastic polymer mixtures using Polyethylene Terephthalate Glycol(PET-G)and a blend of Polycarbonate and Acrylonitrile-Butadiene-Styrene(PC/ABS)with high lignin content(50–60 wt%)is explored,as well as the production of filaments for carbon fiber production.For this purpose,following melt mixing,the lignin-based mixtures were spun into filaments,which were subsequently subjected to thermal stabilization in an oxidative atmosphere.The lignin phase was well distributed in the PET-Gmatrix and the twomaterials presented a good interface,which further improved after thermal treatment under an oxidative atmosphere.After thermal treatment an increase in tensile modulus,tensile strength,and elongation at break of approximately 160%,200%,and 100%,respectively,was observed,confirming the good interface established,and consistent with structural changes such as cross-linking.Conversely,the PC/ABS blend did not form a good interface with the lignin domains after melt mixing.Although the interactions improved after thermal treatment,the tensile strength and elongation at break decreased by approximately 30%,while themodulus increased by approximately 20%.Overall,the good processability of the lignin/polymer mixtures into filaments,and their physical,chemical,and mechanical characterization before and after thermal oxidation are good indicators of the potential as precursors for carbon fiber production.展开更多
基金funded by Project Better Plastics—Plastics in a Circular Economy—PPS4(Circularity by Alternative Feedstocks)Grant agreement ID:POCI-01-0247-FEDER-046091RR was funded by FCT through the PhD grant with reference UI/BD/154446/2022.
文摘The growing environmental awareness,the search for alternatives to fossil resources,and the goal of achieving a circular economy have all contributed to the increasing valorization of biowaste to produce bio-based polymers and other high-value products.Among the various biowaste materials,lignin has gained significant attention due to its high aromatic carbon content,low cost,and abundance.Lignin is predominantly sourced as a byproduct from the paper industry,available in large quantities from hardwood and softwood,with variations in chemical structure and susceptibility to hydrolysis.This study focuses on softwood lignin obtained through the LignoForce^(TM) technology,comparing the thermal and chemical characteristics,and stability,of a recently produced batch with that of a batch that has been stored for four years.Additionally,the development of lignin-based thermoplastic polymer mixtures using Polyethylene Terephthalate Glycol(PET-G)and a blend of Polycarbonate and Acrylonitrile-Butadiene-Styrene(PC/ABS)with high lignin content(50–60 wt%)is explored,as well as the production of filaments for carbon fiber production.For this purpose,following melt mixing,the lignin-based mixtures were spun into filaments,which were subsequently subjected to thermal stabilization in an oxidative atmosphere.The lignin phase was well distributed in the PET-Gmatrix and the twomaterials presented a good interface,which further improved after thermal treatment under an oxidative atmosphere.After thermal treatment an increase in tensile modulus,tensile strength,and elongation at break of approximately 160%,200%,and 100%,respectively,was observed,confirming the good interface established,and consistent with structural changes such as cross-linking.Conversely,the PC/ABS blend did not form a good interface with the lignin domains after melt mixing.Although the interactions improved after thermal treatment,the tensile strength and elongation at break decreased by approximately 30%,while themodulus increased by approximately 20%.Overall,the good processability of the lignin/polymer mixtures into filaments,and their physical,chemical,and mechanical characterization before and after thermal oxidation are good indicators of the potential as precursors for carbon fiber production.
