Direct 3D Printing of Catalytically Active Structures

被引:51
|
作者
Manzano, J. Sebastian
Weinstein, Zachary B.
Sadow, Aaron D.
Slowing, Igor I. [1 ]
机构
[1] US DOE, Ames Lab, Ames, IA 50011 USA
来源
ACS CATALYSIS | 2017年 / 7卷 / 11期
关键词
3D printing; additive manufacturing; catalysis; polymeric materials; millifluidics; STABLE CARBONIUM-IONS; COOPERATIVE CATALYSIS; PERIODIC STRUCTURES; ALDOL CONDENSATION; CHEMICAL-SYNTHESIS; FUNCTIONAL-GROUPS; MANNICH REACTIONS; REACTIONWARE; MICROFLUIDICS; FABRICATION;
D O I
10.1021/acscatal.7b02111
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
3D printing of materials with active functional groups can provide custom-designed structures that promote chemical conversions. Herein, catalytically active architectures were produced by photo polymerizing bifunctional molecules using a commercial stereolithographic 3D printer. Functionalities in the monomers included a polymerizable vinyl group to assemble the 3D structures and a secondary group to provide them with active sites. The 3D-printed architectures containing accessible carboxylic acid, amine, and copper carboxylate functionalities were catalytically active for the Mannich, aldol, and Huisgen cycloaddition reactions, respectively. The functional groups in the 3D-printed structures were also amenable to postprinting chemical modification. As proof of principle, chemically active cuvette adaptors were 3D printed and used to measure in situ the kinetics of a heterogeneously catalyzed Mannich reaction in a conventional solution spectrophotometer. In addition, 3D printed millifluidic devices with catalytically active copper carboxylate complexes were used to promote azide-alkyne cycloaddition under flow conditions. The importance of controlling the 3D architecture of the millifluidic devices was evidenced by enhancing reaction conversion upon increasing the complexity of the 3D prints.
引用
收藏
页码:7567 / 7577
页数:11
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