Tailoring of a catalyst La0.8Ce0.1Ni0.4Ti0.6O3−δ interlayer via in situ exsolution for a catalytic membrane reactor. Issue 8 (6th May 2021)

• Record Type: Journal Article
• Authors: Luo, Ping; Xu, Zhi; Zheng, Qiankun; Tan, Jinkun; Zhang, Zhicheng; Liu, Zhengkun; Zhang, Guangru; Jin, Wanqin
• Is Part Of: Reaction chemistry & engineering. Volume 6:Issue 8(2021)
• Page Start: 1395
• Page End: 1403
• Publication Date: 2021-05-06
• Subjects: Reaction mechanisms (Chemistry) -- Periodicals; Chemical engineering -- Periodicals; Chemical engineering; Reaction mechanisms (Chemistry); Periodicals; 547.705
• DOI: 10.1039/d1re00103e
• Languages: English
• ISSNs: 2058-9883

Abstract

Abstract : Tailored nickel nanoparticles on La0.8 Ce0.1 Ni0.4 Ti0.6 O3− δ surfaces were prepared by in situ exsolution and used in the Ba0.5 Sr0.5 Co0.8 Fe0.2 O3− δ catalytic membrane reactor for high-efficient partial oxidation of methane. Abstract : The application of catalytic membrane reactors (CMRs) based on a perovskite-type oxygen-permeable membrane has been greatly limited by the instability of a membrane material. In this study, A-site deficient perovskite La0.8 Ce0.1 Ni0.4 Ti0.6 O3− δ (LCNT) as a modification porous interlayer (between a Ni/Al2 O3 catalyst and membrane) was applied on a Ba0.5 Sr0.5 Co0.8 Fe0.2 O3− δ (BSCF) four-channel hollow fiber membrane to construct a CMR. Ni nanoparticles were in situ exsolved from the LCNT surfaces and used for partial oxidation of methane (POM). The porous LCNT layer shows excellent attachment, effective protection and enhanced catalytic activity to the BSCF four-channel hollow fiber membrane. The LCNT/BSCF CMR shows a more than 700 h stability in POM which is much higher than that without the modification of the LCNT porous layer (which is less than 150 h). At 900 °C, more than 99% CH4 conversion and CO selectivity have been achieved in the LCNT/BSCF CMR. Our results have demonstrated the feasibility of coupling an in situ exsolution Ni nano-catalyst porous layer with the perovskite-type membrane, providing a new strategy for enhancing both the stability and catalytic activity of CMRs.