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Unlocking the Potential of CO 2 Capture: A Synergistic Hybridization Strategy for Polymeric Hydrogels with Tunable Physicochemical Properties.

Yucong GuGaopeng WangXuanzhou ChenXiaohan XuYanghe LiuJintao YangDong Zhang
Published in: Small (Weinheim an der Bergstrasse, Germany) (2024)
Unlocking CO 2 capture potential remains a complex and challenging endeavor. Here, a blueprint is crafted for optimizing materials through CO 2 capture and developing a synergistic hybridization strategy that involves synthesizing CO 2 -responsive hydrogels by integrating polymeric networks interpenetrated with polyethyleneimine (PEI) chains and inorganic CaCl 2 . Diverging from conventional CO 2 absorbents, which typically serve a singular function in CO 2 capture, these hybrid PEAC hydrogels additionally harness its presence to tune their optical and mechanical properties once interacting with CO 2 . Such synergistic functions entail two significant steps: (i) rapid CO 2 -fixing through PEI chains to generate abundant carbamic acid and carbamate species and (ii) mineralization via CaCl 2 to induce the formation of CaCO 3 micro-crystals within the hydrogel matrix. Due to the reversible bonding, the PEAC hydrogels enable the decoupling of CO 2 through an acid fumigation treatment or a heating process, achieving dynamic CO 2 capture-release cycles up to 8 times. Furthermore, the polyethyleneimine-acrylamide-calcium chloride (PEAC) hydrogel exhibits varying antibacterial attributes and high interfacial adhesive strength, which can be modulated by fine-tuning the compositions of PEI and CaCl 2 . This versatility underscores the promising potential of PEAC hydrogels, which not only unlocks CO 2 capture capabilities but also offers opportunities in diverse biological and biomedical applications.
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