Mechanochemical Phosphorylation of Polymers and Synthesis of Flame-Retardant Cellulose Nanocrystals

被引:119
|
作者
Fiss, Blaine G. [1 ]
Hatherly, Lucius [1 ]
Stein, Robin S. [1 ]
Friscic, Tomislav [1 ]
Moores, Audrey [1 ]
机构
[1] McGill Univ, Ctr Green Chem & Catalysis, Dept Chem, 801 Sherbrooke St West, Montreal, PQ H3A 0B8, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
mechanochemistry; biomass; coating; surface modification; solid-state synthesis; solvent-free; THERMAL-DEGRADATION; ACID; PHOSPHORUS; SYSTEM; LEGACY;
D O I
10.1021/acssuschemeng.9b00764
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Phosphorylated polymers are versatile materials for a broad range of applications from flame-retardant coatings to bioactive scaffolds. Traditionally, they are synthesized in solution using corrosive concentrated phosphoric acid and energy intensive drying techniques. In the past decade, mechanochemistry has proven to be a valuable tool for green chemists to conduct new transformations, with minimal waste, often solvent-free. This work presents the phosphorylation of cellulose nanocrystals, poly(ethylene glycol), poly(vinyl alcohol), poly(vinyl chloride), and lignin through mechanochemical processes with phosphorus pentoxide to produce reproducible phosphorylation for potential flame-retardant applications. Through P-31 magic angle spinning (MAS) NMR, loadings of up to 3300 mmol/kg were determined for cellulose nanocrystals, far superior to loadings in solution around 1600 mmol/kg, and loadings of up to 4375 mmol/kg were obtained for synthetic polymers such as poly(vinyl alcohol).
引用
收藏
页码:7951 / 7959
页数:17
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