Role of Water on Zeolite-Catalyzed Dehydration of Polyalcohols and EVOH Polymer

被引:11
作者
Chau, Han K. [1 ]
Nguyen, Quy P. [1 ]
Jerdy, Ana Carolina [1 ]
Bui, Dai-Phat [1 ]
Lobban, Lance L. [1 ]
Wang, Bin [1 ]
Crossley, Steven P. [1 ]
机构
[1] Univ Oklahoma, Sch Chem Biol & Mat Engn, Norman, OK 73019 USA
基金
美国国家科学基金会;
关键词
polymer upcycling; zeolites; dehydration; water effect; competitive adsorption; BRONSTED-ACID SITE; GAMMA-VALEROLACTONE; THERMAL-DEGRADATION; ETHANOL DEHYDRATION; CHABAZITE ZEOLITES; AB-INITIO; FRAMEWORK; CRACKING; SOLVATION; PROXIMITY;
D O I
10.1021/acscatal.2c05303
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Selective dehydration of polyalcohols over zeolites containing Bri nsted acids is a promising approach to purify and recycle multilayer polymer films consisting of non-polar polymers such as polyethylene and polar polymers like ethylene-vinyl alcohol copolymer. In addition, polar aprotic solvents can be utilized to improve the diffusion of polymer molecules to access the active sites in solid catalysts. Here, we reveal the positive role of water on dehydration of ethylene-vinyl alcohol polymer over a solid acid catalyst in the presence of gamma-valerolactone as the solvent. Through vapor-phase experiments with 2,5-hexanediol as a model compound and theoretical calculations, we reveal that water facilitates dehydration reactions by delocalizing surface-bound protons and allowing dehydration rates to occur even in the presence of solvents that would otherwise inhibit reaction rates. The hydronium ion clusters act as delocalized acid sites, leading to improved surface coverage of the reactant, and consequently enhance dehydration activity in the presence of solvent molecules. This example of co-solvent-induced modulation of environments around active sites could open doors for polymer recycling and upcycling.
引用
收藏
页码:1503 / 1512
页数:10
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