材料科学
吸附
聚合物
化学工程
芴
热重分析
热稳定性
解吸
分散性
高分子化学
有机化学
化学
复合材料
工程类
作者
Noorullah Baig,Suchetha Shetty,Sk Abdul Wahed,Atikur Hassan,Neeladri Das,Bassam Alameddine
标识
DOI:10.1021/acsami.4c02948
摘要
Three novel conjugated porous organic polymers, denoted as C-POP1–3 and which consist of alternating pyrene cores with various contorted fluorene surrogates, were successfully synthesized from a versatile one-pot palladium-catalyzed [3+2] cyclocondensation reaction. The resulting polymers were obtained in excellent yields and displayed weight-average molecular weights (Mw) ranging from 12.2 to 20.2 kg/mol with polydispersity indices (Mw/Mn) ranging between 1.8 and 2.4, suggesting that the molecular masses are narrowly distributed and thus implying homogeneous polymer chains. Thermal stability exploration of C-POP1–3 by thermogravimetric analysis (TGA) revealed an impressive robustness with a 10% weight reduction temperature attaining 485 °C. Investigation of the inherent microporosity properties of C-POP1–3 via nitrogen adsorption experiments using Brunauer–Emmett–Teller (BET) theory discloses their surface areas which reach up to 560 m2 g–1 and pore volumes averaging 0.47 cm3 g–1. The target conjugated polymers were explored as adsorbents disclosing a maximum carbon dioxide adsorption of 83.0 mg g–1 at 273 K and low pressure for C-POP1, whereas iodine sorption tests portrayed prominent outcomes, notably for C-POP3 which proved to owe a strong affinity toward the hitherto mentioned halogen by achieving a maximum adsorption of 2220 mg g–1. Additionally, recyclability experiments confirmed the possibility to regenerate the polymers' adsorption capabilities even after seven consecutive cycles of adsorption–desorption cycles, which qualify them as auspicious iodine adsorbents.
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