Scalable Pickering Stabilization to Design Cellulose Nanofiber-wrapped Block Copolymer Microspheres for Thermal Energy Storage

被引:22
作者
Chakrabarty, Arindam [1 ]
Teramoto, Yoshikuni [1 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Div Forest & Biomat Sci, Kyoto 6068502, Japan
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2020年 / 8卷 / 11期
基金
日本学术振兴会; 日本科学技术振兴机构; 奥地利科学基金会;
关键词
Cationic cellulose nanofiber; Ultrasound-free Pickering emulsion; Thermal energy storage; Block copolymer; PHASE-CHANGE MATERIALS; MICROENCAPSULATED PARAFFIN; CHANGE COMPOSITES; EMULSION; SHELL; MINIEMULSION; NANOCOMPOSITE; ENCAPSULATION; NANOCRYSTALS; STABILITY;
D O I
10.1021/acssuschemeng.0c00687
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The only limitation to scale up the preparation of Pickering emulsion is the ultrasonication step. In this study, a scalable ultrasound-free approach was adopted to make a stable oilin-water (o/w) Pickering emulsion using cationic cellulose nanofibers (cNFs) as a stabilizer. The formation and stability of the emulsions were entirely dependent on the degree of cationic substitution (DS) in cNFs. Using such emulsions, we developed an aqueous dispersion of block copolymer (BCP)/cNF nanocomposite having the ability to store thermal energy. The BCP was prepared by reversible addition-fragmentation chain transfer ( RAFT) polymerization of stearyl methacrylate (SMA) followed by the polymerization of methyl methacrylate (MMA) in cNF-stabilized Pickering emulsion. The polySMA (PSMA) segment in the nanocomposite exhibited the ability to absorb and release thermal energy due to the side-chain melting and crystallization. The stability of the Pickering emulsion and nanocomposite latex along with the respective yields were greatly dependent on the DS in cNFs. Interestingly, the cNF-stabilized BCPs had the crystalline melting at 34-37 degrees C and crystallization at 22-28 degrees C with 12-fold higher latent heat than the BCP stabilized by sodium dodecylsulfate (SDS), a conventional surfactant.
引用
收藏
页码:4623 / 4632
页数:10
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