Broadening synthetic scope of SSZ-39 zeolite for NH3-SCR: A fast and direct route from amorphous starting materials

被引:14
作者
Hu, Peidong [1 ,2 ]
Iyoki, Kenta [2 ]
Fujinuma, Haruko [1 ]
Yu, Jingyun [2 ]
Yu, Sijing [2 ]
Anand, Chokkalingam [1 ]
Yanaba, Yutaka [3 ]
Okubo, Tatsuya [2 ]
Wakihara, Toru [1 ,2 ]
机构
[1] Univ Tokyo, Inst Engn Innovat, Bunkyo Ku, 2-11-16 Yayoi, Tokyo 1138656, Japan
[2] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[3] Univ Tokyo, Inst Ind Sci, Meguro Ku, 4-6-1 Komaba, Tokyo 1538505, Japan
基金
日本学术振兴会;
关键词
SSZ-39; Zeolites; Hydrothermal synthesis; Hydrothermal stability; Selective catalytic reduction; SEED-ASSISTED SYNTHESIS; CHA-TYPE ZEOLITE; ULTRAFAST SYNTHESIS; INTERZEOLITE CONVERSION; METHANOL; FAU; AEI; CATALYST; CRYSTALLIZATION; CU-SSZ-39;
D O I
10.1016/j.micromeso.2021.111583
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The inevitable use of FAU-type zeolites and long synthesis time bottleneck the mass production of SSZ-39 zeolite, a next-generation catalyst for selective catalytic reduction of NOx by ammonia (NH3-SCR). Herein, fast synthesis of SSZ-39 zeolites directly from colloidal silica and sodium aluminate is achieved with various reactant compositions, including a cost-effective low organic structure-directing agent-consuming condition and a scarcely reported KOH-containing condition. The reactant alkalinity and NaOH content are critical to the phase selectivity and fast crystallization, and partially replacing Na+ with K+ can eliminate the formation of gmelinite impurity. With optimized conditions, synthesis can be completed within 4 h without aging process in an autoclave, and even within 80 min by fast heating in a tubular reactor. Outstanding hydrothermal stability and NH3-SCR activity of the Cu-exchanged samples prove such fast and direct synthesis route a promising way to efficiently produce high-quality SSZ-39 zeolites for further applications.
引用
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页数:9
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