Sulfated and carboxylated nanocellulose for Co+2 adsorption

纳米纤维素 材料科学 纳米纤维 络腮胡子 结晶度 表面改性 水溶液 硫酸 化学工程 吸附 纤维素 水解 接触角 核化学 有机化学 复合材料 冶金 化学 工程类
作者
Lucas Tonette Teixeira,Wanderson Ferreira Braz,Rogério Navarro Correia de Siqueira,Omar Pandoli,Mauro César Geraldes
出处
期刊:Journal of materials research and technology [Elsevier BV]
卷期号:15: 434-447 被引量:17
标识
DOI:10.1016/j.jmrt.2021.07.123
摘要

Regarding metals adsorption from aqueous solutions, nanocellulose emerges as a potential material, due to the many functionalization possibilities and enhanced surface contact area (nanostructured nature). In the present work, sulfated and carboxylated nanocellulose samples were obtained through sulfuric acid hydrolysis (S-CNC) and oxidation by TEMPO (CNF). The obtained nanofibers were characterized through multiple techniques, which XRD data indicated the presence of α-cellulose crystals, with crystallinity indexes equal to 72.3% (S-CNC) and 69.3% (CNF). Expressive morphological differences were revealed, whiskers particles for S-CNC, and elongated nanofibrils for CNF, with average thickness of 9.99 and 5.61 nm, respectively. The desired functionalization with carboxylate groups was evidenced based on FTIR data (CNF). A significant and homogeneous presence of sulfur was evidenced through SEM/EDS (S-CNC). The synthesized nanofibers were next applied to cobalt (Co+2) adsorption from aqueous solutions at room temperature. On both cases, expressive maximum cobalt recoveries have been achieved, 90% (CNF) and 87% (S-CNC), for contact times higher than 30 and 45 min, respectively. The adsorptive capacities evaluated through ICP-OES from liquid phase data (87 mg g−1 S-CNC; 90 mg g−1 CNF) were both significantly higher than the values determined through LA-ICP-MS (10.5 mg Co g−1 S-CNC; 31.5 mg Co g−1 CNF).

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