Sustainable carbon dots comprising surficial oxime ester groups following homolytic bond cleavage exhibit potential as photoinitiators for traditional free radical photopolymerization. Carbon dots were made following a solvothermal procedure from sustainable furfural available from lignocellulose. Surficial aldehyde moieties reacted with hydroxylamine to the respective oxime while reaction with benzoyl chloride resulted in a biobased Type I photoinitiator comprising sustainable carbon dot ( CD ‐ PI ). Photoinitiating ability was compared with the traditional photoinitiator ( PI ) ethyl (2,4,6‐trimethyl benzoyl) phenyl phosphinate ( TPO ‐ L ) by real‐time FTIR with UV exposure at 365 nm. Photopolymer composition based on a mixture of urethane dimethacrylate ( UDMA ) and tripropylene glycol diacrylate ( TPGDA ) resulted in a similar final conversion of about 70 % using either CD‐PI or TPO‐L . Nevertheless, it appeared homogeneous in the case of compositions processed with CD‐PI , while those made with TPO ‐ L were heterogeneous as shown by two glass transition temperatures. Moreover, the migration rate of CD ‐ PI in the cured samples was lower in comparison with those samples using TPO ‐ L as PI .
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Li et al. (2024) studied this question.
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