Thiol-Surface-Engineered Cellulose Nanocrystals in Favor of Copper Ion Uptake

纤维素 硫醇 纳米晶 材料科学 表面改性 化学工程 纳米技术 化学 生物化学 冶金 工程类
作者
Trung Dang‐Bao,Thi-My-Chau Nguyen,Gia-Han Hoang,Hoa-Hung Lam,Hong-Phuong Phan,Thi-Kieu-Anh Tran
出处
期刊:Polymers [MDPI AG]
卷期号:15 (11): 2562-2562 被引量:11
标识
DOI:10.3390/polym15112562
摘要

Cellulose, the most abundant natural polymer on earth, has recently gained attention for a large spectrum of applications. At a nanoscale, nanocelluloses (mainly involving cellulose nanocrystals or cellulose nanofibrils) possess many predominant features, such as highly thermal and mechanical stability, renewability, biodegradability and non-toxicity. More importantly, the surface modification of such nanocelluloses can be efficiently obtained based on the native surface hydroxyl groups, acting as metal ions chelators. Taking into account this fact, in the present work, the sequential process involving chemical hydrolysis of cellulose and autocatalytic esterification using thioglycolic acid was performed to obtain thiol-functionalized cellulose nanocrystals. The change in chemical compositions was attributed to thiol-functionalized groups and explored via the degree of substitution using a back titration method, X-ray powder diffraction, Fourier-transform infrared spectroscopy and thermogravimetric analysis. Cellulose nanocrystals were spherical in shape and ca. 50 nm in diameter as observed via transmission electron microscopy. The adsorption behavior of such a nanomaterial toward divalent copper ions from an aqueous solution was also assessed via isotherm and kinetic studies, elucidating a chemisorption mechanism (ion exchange, metal chelation and electrostatic force) and processing its operational parameters. In contrast to an inactive configure of unmodified cellulose, the maximum adsorption capacity of thiol-functionalized cellulose nanocrystals toward divalent copper ions from an aqueous solution was 4.244 mg g−1 at a pH of 5 and at room temperature.
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