Poly(lactic acid) synthesized from non‐food biomass feedstocks with tin‐loaded ZA molecular sieve catalysts by direct melt polycondensation
Chengtao Gao,
Yanwen Wang,
Yunlong Yang
et al.
Abstract:The design and synthesis of catalysts loaded with active components has attracted considerable attention in current research owing to their exceptional catalytic performance. In this study, the focus was on the utilization of tin‐loaded ZA molecular sieves, possessing remarkable adsorption properties, alongside the catalytic activity of tin. These catalysts were successfully prepared and employed for the synthesis of poly(lactic acid) (PLA) from lactic acid derived from non‐food biomass. By modifying the treat… Show more
The ring-opening polymerization of L-lactide is a crucial route for producing biodegradable polylactides (PLAs). Developing an efficient catalyst for this process poses significant challenges. Herein, we report the successful incorporation of nickel during the crystallization of ZIF-67, the derivation of the abundant and stable CoO source, to obtain the composite magnetic Ni@CoO@ZIF-67 using the solid-state thermal (SST) method. The characterization of the resulting materials revealed that nickel atoms are well dispersed in the composite CoO@ZIF-67, imparting additional magnetic properties. The composite Ni@CoO@ZIF-67 demonstrated superior performance as a heterogeneous catalyst for the ring-opening polymerization of L-lactide compared to reference materials such as Ni-Hmim, CoO, ZIF-67, and CoO@ZIF-67. Furthermore, the magnetic property of Ni@CoO@ZIF-67 offers practical advantages, enabling easier separation and recycling of the catalyst. Notably, the SST method facilitates the single-step synthesis of composite magnetic Ni@CoO@ZIF-67 under solvent-free conditions, representing a significant advancement in catalyst development. This approach not only simplifies the synthesis process but also inspires further developments of heterogeneous magnetic catalysts for a variety of effective and diverse reactions.
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