Recycling of poly-(methyl methacrylate) waste sheets to synthesize catalyst-free bi-functional cation-exchange resin for sequestering of toxic pollutant
A simple and green method for the recovery of methyl methacrylate (MMA) has been developed by recycling waste sheets of poly-(methyl methacrylate) without using any catalyst. The liquefaction yield was 97.33% while the purity of recovered MMA was up to 92%. The recovered monomer utilized for the syn...
Gespeichert in:
Veröffentlicht in: | Polymer bulletin (Berlin, Germany) Germany), 2024-09, Vol.81 (14), p.12575-12592 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | A simple and green method for the recovery of methyl methacrylate (MMA) has been developed by recycling waste sheets of poly-(methyl methacrylate) without using any catalyst. The liquefaction yield was 97.33% while the purity of recovered MMA was up to 92%. The recovered monomer utilized for the synthesis of methylmethacrylate-copolymer-divinylbenzene at 20% cross-linking in the presence of different porogens (methyl isobutyl ketone, cyclohexane, toluene, and cyclohexanone) by suspension polymerization. The same copolymer was also synthesized but with different cross-linking percentages such as 4, 10, 15, 20, 25, 30, and 40% in the presence of a single porogen (methyl isobutyl ketone). Different copolymers having pore volumes in the range of 0.120–0.682 mL/g were obtained. The pendant –COOCH
3
groups within the polymeric chain were converted to –COOH groups via acid hydrolysis, accompanied by the attachment of –SO
3
H groups to phenyl rings. ATR-FTIR, UV–Vis spectrometry, and HPLC techniques were used for qualitative and quantitative analyses of –COOH and –SO
3
H groups. The obtained results were compared with copolymers and resin synthesized using commercial MMA, displaying similar behavior. The resin derived from the recovered monomer was utilized for Co
2+
ion removal at various pH, demonstrating excellent removal performance. |
---|---|
ISSN: | 0170-0839 1436-2449 |
DOI: | 10.1007/s00289-024-05282-1 |