Degradation behaviour and recovery of bisphenol-A from epoxy resin and polycarbonate resin by liquid-phase chemical recycling

2005 ◽  
Vol 89 (2) ◽  
pp. 317-326 ◽  
Author(s):  
Yoshiki Sato ◽  
Yasuhiko Kondo ◽  
Koji Tsujita ◽  
Noboru Kawai
2013 ◽  
Vol 658 ◽  
pp. 153-157 ◽  
Author(s):  
Yu Yan Liu ◽  
Song Quan Wu ◽  
Li Li ◽  
Yu Ting Liu ◽  
Guo Hua Shan

The degradation behaviour of an anhydride-cured bisphenol A diglycidyl ether (DGEBA) epoxy resin in near-critical water was studied in this paper. The experiments were performed in a stainless steel reactor (100ml) without stirring. Epoxy resin could be decomposed successfully at 270°C for 30 min. The degradation rate of epoxy resin increased with an increase in reaction temperature and reaction pressure. The degradation reaction products were characterized by gas chromatography-mass spectrometry (GC-MS). The degradation reaction was associated with the scission of ester and ether bonds which further destabilizes the epoxy network.


2021 ◽  
Vol 2 (2) ◽  
pp. 419-430
Author(s):  
Ankur Bajpai ◽  
James R. Davidson ◽  
Colin Robert

The tensile fracture mechanics and thermo-mechanical properties of mixtures composed of two kinds of epoxy resins of different chemical structures and functional groups were studied. The base resin was a bi-functional epoxy resin based on diglycidyl ether of bisphenol-A (DGEBA) and the other resins were (a) distilled triglycidylether of meta-amino phenol (b) 1, 6–naphthalene di epoxy and (c) fluorene di epoxy. This research shows that a small number of multifunctional epoxy systems, both di- and tri-functional, can significantly increase tensile strength (14%) over neat DGEBA while having no negative impact on other mechanical properties including glass transition temperature and elastic modulus. In fact, when compared to unmodified DGEBA, the tri-functional epoxy shows a slight increase (5%) in glass transition temperature at 10 wt.% concentration. The enhanced crosslinking of DGEBA (90 wt.%)/distilled triglycidylether of meta-amino phenol (10 wt.%) blends may be the possible reason for the improved glass transition. Finally, the influence of strain rate, temperature and moisture were investigated for both the neat DGEBA and the best performing modified system. The neat DGEBA was steadily outperformed by its modified counterpart in every condition.


2021 ◽  
Vol 92 (4) ◽  
pp. 044103
Author(s):  
Chase A. Salazar ◽  
Blaise J. Thompson ◽  
Spring M. M. Knapp ◽  
Steven R. Myers ◽  
Shannon S. Stahl

ChemSusChem ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 1184-1195
Author(s):  
Saeid Nikafshar ◽  
Jiarun Wang ◽  
Kevin Dunne ◽  
Prakit Sangthonganotai ◽  
Mojgan Nejad

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1722
Author(s):  
Troy Semelsberger ◽  
Jason Graetz ◽  
Andrew Sutton ◽  
Ewa C. E. Rönnebro

We present the research findings of the DOE-funded Hydrogen Storage Engineering Center of Excellence (HSECoE) related to liquid-phase and slurry-phase chemical hydrogen storage media and their potential as future hydrogen storage media for automotive applications. Chemical hydrogen storage media other than neat liquid compositions will prove difficult to meet the DOE system level targets. Solid- and slurry-phase chemical hydrogen storage media requiring off-board regeneration are impractical and highly unlikely to be implemented for automotive applications because of the formidable task of developing solid- or slurry-phase transport systems that are commercially reliable and economical throughout the entire life cycle of the fuel. Additionally, the regeneration cost and efficiency of chemical hydrogen storage media is currently the single most prohibitive barrier to implementing chemical hydrogen storage media. Ideally, neat liquid-phase chemical hydrogen storage media with net-usable gravimetric hydrogen capacities of greater than 7.8 wt% are projected to meet the 2017 DOE system level gravimetric and volumetric targets. The research presented herein is a collection of research findings that do not in and of themselves warrant a dedicated manuscript. However, the collection of results do, in fact, highlight the engineering challenges and short-comings in scaling up and demonstrating fluid-phase ammonia borane and alane compositions that all future materials researchers working in hydrogen storage should be aware of.


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