Tetramethylbenzenium radical cations as major active intermediates of methanol-to-olefin conversions over phosphorous-modified HZSM-5 zeolites

• Published in: Journal of catalysis Vol. 299; pp. 240 - 248
• Main Authors: Jang, Hoi-Gu, Min, Hyung-Ki, Hong, Suk Bong, Seo, Gon
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Inc 01.03.2013; Elsevier; Elsevier BV
• Subjects: Catalysis; Catalysts; Chemical compounds; Chemistry; Electron spin resonance; Exact sciences and technology; General and physical chemistry; HZSM-5; Ion-exchange; Methanol; Methanol-to-olefin conversion; Minerals; Phosphorous modification; Phosphorus; Surface physical chemistry; Tetramethylbenzenium radical cations; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Zeolites: preparations and properties; Methanol-to-olefin conversion; Tetramethylbenzenium radical cations; HZSM-5; Electron spin resonance; Phosphorous modification; Reaction intermediate; Alcohol; Phosphorus; Conversion; Heterogeneous catalysis; Olefin; Alkanol; Ethylenic compound; Modified material; Methanol
• ISSN: 0021-9517; 1090-2694
• DOI: 10.1016/j.jcat.2012.12.014

The hyperfine splitting of tetramethylbenzenium radical cations is similar to that of organic species formed in MTO conversions in HZSM-5 pores. [Display omitted] ► Radical cations were formed in methanol-to-olefin conversion over HZSM-5 zeolites. ► Phosphorous modification allowed the observation of their hyperfine splitting. ► Electron spin resonance signals confirm the presence of tetramethylbenzenium cations. ► They worked as major active intermediates in methanol-to-olefin conversions. The reaction intermediates of methanol-to-olefin (MTO) conversion over phosphorous-modified HZSM-5 (P-MFI) catalysts were investigated by electron spin resonance (ESR) and gas chromatography–mass spectroscopy (GC–MS). Phosphorous modification partially neutralized the strong acid sites in HZSM-5. The phosphorous compounds suppress the migration of polymethylbenzenium radical cations, lowering spin–spin interactions and thus preserved their hyperfine splitting. The ESR spectra of the organic species formed in P-MFI zeolites during MTO conversion were similar to those of the cation species generated from 1,2,4,5-tetramethylbenzene in mordenite. GC–MS of organic extracts revealed the predominant formation of polymethylbenzenes with 4–6 methyl groups. The correlation between conversion and the number of spins of tetramethylbenzenium radical cations exhibited that these radical cations might be major active intermediates of MTO conversion over P-MFI catalysts.