Al-Modified Ti-MOR as a robust catalyst for cyclohexanone ammoximation with enhanced anti-corrosion performance. Issue 22 (6th October 2021)
- Record Type:
- Journal Article
- Title:
- Al-Modified Ti-MOR as a robust catalyst for cyclohexanone ammoximation with enhanced anti-corrosion performance. Issue 22 (6th October 2021)
- Main Title:
- Al-Modified Ti-MOR as a robust catalyst for cyclohexanone ammoximation with enhanced anti-corrosion performance
- Authors:
- Peng, Rusi
Wan, Zhipeng
Lv, Huanzhi
Guan, Yejun
Xu, Hao
Wu, Peng - Abstract:
- Abstract : The skeleton desilication accompanied by Ti active sites leaching accounts for the dominant chemical deactivation reasons in the alkali liquid-phase ammoximation, which could be retarded by creating a protective Al-rich shell. Abstract : The skeleton desilication accompanied by Ti active sites leaching accounts for the dominant chemical deactivation reasons during the clean industrial production of cyclohexanone oxime through titanosilicate-catalyzed liquid-phase ammoximation in the alkali reaction system. In this study, aluminum species were reintroduced into Ti-MOR by hydrothermal post-treatment with aluminum salts to enhance its anti-corrosion performance against alkaline medium and catalytic stability in cyclohexanone ammoximation reaction. The undesired strengthening in hydroxylamine decomposition and oxime hydrolysis derived from the implantation of aluminum into the framework could be eliminated via further Na + -exchange. By means of quenching bridging Si(OH)Al-related acidic sites selectively, the exchanged process then enhanced catalytic activity significantly in both the hydroxylamine formation and ammoximation processes. With aluminum species enriched on the crystal shell, Ti-MOR after aluminated and Na + -exchanged (denoted as Al-Ti-M-Na) showed a more robust performance in the simulated desilication process and a tremendously prolonged ammoximation lifetime of 460 h, which was 2.75 times that of pristine Ti-MOR. The unprecedented duration ofAbstract : The skeleton desilication accompanied by Ti active sites leaching accounts for the dominant chemical deactivation reasons in the alkali liquid-phase ammoximation, which could be retarded by creating a protective Al-rich shell. Abstract : The skeleton desilication accompanied by Ti active sites leaching accounts for the dominant chemical deactivation reasons during the clean industrial production of cyclohexanone oxime through titanosilicate-catalyzed liquid-phase ammoximation in the alkali reaction system. In this study, aluminum species were reintroduced into Ti-MOR by hydrothermal post-treatment with aluminum salts to enhance its anti-corrosion performance against alkaline medium and catalytic stability in cyclohexanone ammoximation reaction. The undesired strengthening in hydroxylamine decomposition and oxime hydrolysis derived from the implantation of aluminum into the framework could be eliminated via further Na + -exchange. By means of quenching bridging Si(OH)Al-related acidic sites selectively, the exchanged process then enhanced catalytic activity significantly in both the hydroxylamine formation and ammoximation processes. With aluminum species enriched on the crystal shell, Ti-MOR after aluminated and Na + -exchanged (denoted as Al-Ti-M-Na) showed a more robust performance in the simulated desilication process and a tremendously prolonged ammoximation lifetime of 460 h, which was 2.75 times that of pristine Ti-MOR. The unprecedented duration of Al-Ti-M-Na was mainly ascribed to the protective effect of the Al-rich shell as it served as the guardian crust that defended the Ti active sites against leaching caused by desilication and skeleton destruction. … (more)
- Is Part Of:
- Catalysis science & technology. Volume 11:Issue 22(2021)
- Journal:
- Catalysis science & technology
- Issue:
- Volume 11:Issue 22(2021)
- Issue Display:
- Volume 11, Issue 22 (2021)
- Year:
- 2021
- Volume:
- 11
- Issue:
- 22
- Issue Sort Value:
- 2021-0011-0022-0000
- Page Start:
- 7287
- Page End:
- 7299
- Publication Date:
- 2021-10-06
- Subjects:
- Catalysis -- Periodicals
541.395 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/CY ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1cy01396c ↗
- Languages:
- English
- ISSNs:
- 2044-4753
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3090.943100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 19816.xml