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).

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
刚刚
张慧慧发布了新的文献求助10
刚刚
苏城完成签到,获得积分10
2秒前
2秒前
蔡demon发布了新的文献求助10
2秒前
2秒前
3秒前
吴谷杂粮发布了新的文献求助10
3秒前
3秒前
3秒前
4秒前
木木老师完成签到,获得积分10
4秒前
4秒前
芋圆发布了新的文献求助10
5秒前
5秒前
5秒前
5秒前
NexusExplorer应助沛沛采纳,获得10
5秒前
愉快的亦云关注了科研通微信公众号
5秒前
5秒前
6秒前
czz发布了新的文献求助10
6秒前
朝夕完成签到,获得积分10
6秒前
小树苗1020完成签到,获得积分10
7秒前
舒心飞珍发布了新的文献求助10
7秒前
jia7发布了新的文献求助10
7秒前
myjf发布了新的文献求助10
7秒前
噢噢噢噢发布了新的文献求助10
7秒前
斯文败类应助木木采纳,获得10
8秒前
8秒前
xxp完成签到 ,获得积分10
8秒前
苗条盼芙发布了新的文献求助10
8秒前
8秒前
KKK研完成签到,获得积分10
8秒前
隋玉完成签到,获得积分10
8秒前
9秒前
农大馒头发布了新的文献求助10
9秒前
边瑞明关注了科研通微信公众号
9秒前
chengshaoyan发布了新的文献求助10
9秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
Contemporary Debates in Epistemology (3rd Edition) 1000
International Arbitration Law and Practice 1000
文献PREDICTION EQUATIONS FOR SHIPS' TURNING CIRCLES或期刊Transactions of the North East Coast Institution of Engineers and Shipbuilders第95卷 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6155194
求助须知:如何正确求助?哪些是违规求助? 7983702
关于积分的说明 16589147
捐赠科研通 5265446
什么是DOI,文献DOI怎么找? 2809802
邀请新用户注册赠送积分活动 1789879
关于科研通互助平台的介绍 1657459