Porous Carbon Fiber Functionalization and Thermochemical Degradation of Polystyrene-based Plastics for Resource Recovery

dc.contributor.authorZhang, Yueen
dc.contributor.committeechairLiu, Guoliangen
dc.contributor.committeememberMadsen, Louis Alberten
dc.contributor.committeememberQuan, Linaen
dc.contributor.committeememberLin, Fengen
dc.contributor.departmentChemistryen
dc.date.accessioned2025-12-24T09:01:30Zen
dc.date.available2025-12-24T09:01:30Zen
dc.date.issued2025-12-23en
dc.description.abstractThis dissertation explores the chemical transformation of polyacrylonitrile (PAN)- and polystyrene (PS)-based polymers into sustainable functional materials and chemical products. The research is motivated by two global challenges: the increasing demand for rare earth elements (REEs) for high technology applications and the environmental issues caused by plastic waste accumulation. First, porous carbon fiber (PCF) derived from PAN-based block copolymer was synthesized and functionalized for the extraction of REEs. Second, the thermochemical degradation of PS and PS-based engineering plastic into benzene and alkylbenzene were explored. In the first project, a greener REE leaching method followed by solid-phase extraction using functionalized PCF was developed. To dissolve REE in NdFeB magnets, citrate-assisted leaching was developed and achieved over 90% leaching efficiency, reducing the use of mineral acid. A block copolymer-based PCF with high surface area and well-controlled porous structure was synthesized and functionalized with diglycolamide (DGA) ligands. Two different functionalization strategies, using silane-modified and azide-modified DGA, were employed. Although functionalization of PCF with both strategies was successful, limited improvement in extraction capacity was achieved. The poor performance was attributed to low ligand loading, partial pore blocking, and strong citrate-REE complex interaction. This study provided PCF functionalization strategies but showed challenges of REE extraction with functionalized PCF as an adsorbent. The second project focused on the degradation of PS into benzene and its subsequent upcycling into alkylbenzene. PS was thermochemically degraded using AlCl3 as a catalyst to produce benzene. The effect of Lewis acid type, solvent, and AlCl3 concentration was investigated. The optimized reaction conditions for benzene production were identified as 100 mol% AlCl3 in cyclohexane at 100 °C for 5 h. The recovered benzene was further upcycled to alkylbenzene by Friedel-Crafts alkylation with 1-dodecene or 1-chlorodedecane. Both one-step and two-step alkylation reactions for alkylbenzene production were explored, but a low alkylbenzene yield was achieved. GC-MS analysis revealed the formation of alkylbenzene isomers and alkane side products, indicating low selectivity and competing side reactions as the limitation of alkylbenzene production. The third project extended the thermochemical degradation strategy to an engineering plastic, acrylonitrile-butadiene-styrene (ABS), containing a PS block. Compared with PS, ABS is a multiphase polymer, containing two other polymer blocks, PS and polybutadiene (PBD), which make the degradation pathway more complicated. Under similar conditions of PS degradation using AlCl3, the benzene yield was lower in ABS degradation. Size exclusive chromatography (SEC) analysis revealed the incomplete degradation with crosslinked structures. The effect of solvent on benzene yield was investigated, showing that the benzene yield was affected by both aromaticity of the solvent and the solvent-AlCl3 interactions. Deuterated benzene as an aromatic solvent enhanced benzene yield due to charge-transfer interaction with AlCl3. Degradation studies on PAN and PBD homopolymers showed that both PAN and PBD underwent partial backbone degradation, forming short-chain fragments. Nitrile groups in PAN remained intact, and PBD underwent crosslinking. These results showed that non-PS blocks altered the degradation pathways and hindered the benzene production. Overall, this dissertation advances the understanding of polymer-derived porous carbon materials and thermochemical plastic degradation for sustainable material recovery. While challenges remain in the improvement of REE extraction capacity and achieving high alkylbenzene and benzene yield, the results highlighted the potential of PCF-based adsorbents for REE extraction and thermochemical degradation pathways for plastic recycling. These studies not only provide fundamental insights into structure-property relationships but also suggest future directions toward greener and more efficient strategies for addressing critical metal recovery and plastic waste management.en
dc.description.abstractgeneralThis dissertation focuses on developing new ways to recover rare earth elements (REEs) and recycle plastic waste. REEs are critical metals used in electronics, clean energy, and high-tech devices. The increasing production and poor waste management lead to the accumulation of plastic waste. The research combines chemistry and material science to develop innovative materials and to transform plastic waste into useful products in more sustainable ways. In the first project, recovery of REEs from magnets using a porous carbon material was studied. REEs have unique properties and are widely used in magnets, catalysts, and electronic technologies. The increasing demand for REEs and pollution caused by industrial mining showed the necessity of developing new materials for REE extraction. A greener alternative, citric acid, was used to dissolve REE from magnets, reducing the use of strong mineral acid and the production of hazardous waste. Then, porous carbon fiber (PCF) with a high surface area and porous structure was synthesized. The surface of PCF was modified with ligands for the binding of REE ions. High leaching efficiency using citric acid was achieved and carbon fiber surface modification was successful. However, the extraction capacity of REE with modified carbon fiber was limited. This was due to the low available binding sites on carbon fiber, blocked pores, and interference of other chemical species in the solution. The study showed the potential of porous carbon fiber used for metal extraction, but further optimization is needed. The second project focused on turning polystyrene (PS) into linear alkylbenzene for the application of detergents. PS is a widely used plastic in food containers and packaging. Common plastic management includes burying in landfill or incineration to produce energy. These strategies will cause the accumulation of plastic waste or the generation of greenhouse gases. The development of chemical degradation and upcycling methods for plastic waste management is important to solve the environmental problems. In this study, PS was degraded using AlCl3 as a catalyst and converted into benzene, a useful chemical in industry. The reaction conditions, such as catalyst type, catalyst concentration, and solvent, were explored. Then, efforts were made to upcycle benzene to alkylbenzene, a compound used in detergents, by reacting benzene with 1-dodecene or 1-chlorododecane. Alkylbenzene was produced, but the overall yield was low with the presence of side reactions. This project shows the potential of plastic degradation and upcycling to produce higher value chemicals, but the improvement of the reaction process is needed for better efficiency. The third project extended the degradation to a more complex plastic, acrylonitrile-butadiene-styrene (ABS) under similar conditions of PS degradation. ABS is widely used in consumer goods, electronics, automotive components, and 3D printing filaments. ABS contains the same building block as PS, and also contains two other blocks, PAN and polybutadiene (PBD). The PAN and PBD blocks in ABS improved its mechanical properties and chemical resistance, but it also makes the degradation of ABS more difficult. In this project, benzene was generated from ABS degradation, but with a lower yield than that of PS degradation. The plastic was partially degraded and formed crosslinking structures. The effect of the solvent was studied, and the highest yield was achieved in deuterated benzene. The benzene yield was affected by the structure of the solvent and the solvent-catalyst interaction. Further experiments on the individual components of ABS were conducted and showed that PAN was chemically stable, while PBD was partially crosslinked. These findings explained why engineering plastics like ABS are difficult to recycle, and further studies on ABS degradation pathways are needed. In summary, this dissertation demonstrated new approaches to turning porous carbon fibers and plastic waste into useful materials for resource recovery. The REE extraction by modified porous carbon fiber and the degradation of plastics such as PS and ABS into valuable chemicals were explored. This work highlights the potential of sustainable materials development. The results also showed challenges of these strategies, offering insights to guide future innovation towards critical metal recovery and plastic waste management.en
dc.description.degreeDoctor of Philosophyen
dc.format.mediumETDen
dc.identifier.othervt_gsexam:44806en
dc.identifier.urihttps://hdl.handle.net/10919/140563en
dc.language.isoenen
dc.publisherVirginia Techen
dc.rightsIn Copyrighten
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en
dc.subjectPorous carbon fiberen
dc.subjectrare earth elementsen
dc.subjectdiglycolamide functionalizationen
dc.subjectpolystyreneen
dc.subjectacrylonitrile-butadiene-styreneen
dc.subjectplastic recyclingen
dc.subjectthermochemical degradationen
dc.titlePorous Carbon Fiber Functionalization and Thermochemical Degradation of Polystyrene-based Plastics for Resource Recoveryen
dc.typeDissertationen
thesis.degree.disciplineChemistryen
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen
thesis.degree.leveldoctoralen
thesis.degree.nameDoctor of Philosophyen

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