Formation Pathway of By-products in Methacrolein Oxidation over H3PMo12O4o Investigated by Using 13C-Labeled Methacrolein

Kanno, Mitsuru; Hirata, Jun; Umezawa, Taiki et al.

Journal of the Japan Petroleum Institute, 2023, 66(4), 128-131

Permalink : https://hdl.handle.net/2115/90338

このアイテムのアクセス数:931件（2026-01-13 05:42 集計）

ファイル	フォーマット	サイズ	閲覧回数	説明
66_128	pdf	377 KB	142	本文
66_128_1	pdf	278 KB	103	Supporting Information

アクセス権	open access
URI	https://hdl.handle.net/2115/90338
タイトル	Formation Pathway of By-products in Methacrolein Oxidation over H3PMo12O4o Investigated by Using 13C-Labeled Methacrolein
著者	Kanno, Mitsuru ; Hirata, Jun ; Umezawa, Taiki ; Ninomiya, Wataru ; Kamiya, Yuichi
著者名 Kanno, Mitsuru
著者名 Hirata, Jun
e-Rad_Researcher 20503618 著者名 Umezawa, Taiki
著者名 Ninomiya, Wataru
e-Rad_Researcher 10374638 著者名 Kamiya, Yuichi
言語	英語
キーワード	Methacrolein oxidation
	Heteropoly acid
	Isotopic labeling method
	Reaction mechanism
	Acetic acid
発行日	2023-07-01
出版者	Japan Petroleum Institute
収録物名	Journal of the Japan Petroleum Institute
巻(号)	66(4)
ページ	128-131
抄録	Understanding the mechanism for the formations of by-products as well as a main product can give us useful information for improvement in the catalytic performances. In the present study, formation pathway of by-products in oxidation of methacrolein (MAL) was investigated by using MAL with 13C-labeled methyl group as a reactant. The reaction pathway for the formation of the by-products was proposed based on GC-MS analysis as follows: The first step is oxidative cleavage of C=C double bond in MAL, giving pyruvaldehyde, and pyruvaldehyde is subsequently hydrolyzed to acetic acid.
資源タイプ	学術雑誌論文
出版タイプ	Version of Record
PISSN	1346-8804
EISSN	1349-273X
関連情報 (isIdenticalTo)	出版社版DOI https://doi.org/10.1627/jpi.66.128