{"title":"Catalytic hydrodenitrogenation of primary, secondary, and tertiary C12-alkyl amines over a platinum on zirconia catalyst","authors":"Joakim, Kattelus, Leoni-Franziska, Klingelhöfer, Emma, Verkama, Jorge, Velasco, Leonhard, Iser, Marcus, Rose, Reetta, Karinen, Riikka, Puurunen","doi":"10.26434/chemrxiv-2024-z1kc3","DOIUrl":null,"url":null,"abstract":"In this work, the hydrodenitrogenation (HDN) of a primary amine (dodecylamine), a secondary amine (didodecylamine), and a tertiary amine (tridodecylamine) over a Pt/ZrO2 catalyst was compared in a batch reactor. The main product of the amine hydrotreating was dodecane, but significant amounts of secondary amine were also formed as an intermediate during HDN of the primary and the tertiary amine. It was found that the primary amine is the only species for which direct HDN is possible; HDN of the secondary amine thus proceeds through a primary amine intermediate and HDN of the tertiary amine involves formation of secondary amine, which decomposes to primary amine. Consequently, HDN of the tertiary and secondary amines is slower than that of the primary amine. Kinetic modeling indicated that bimolecular condensation reactions of the primary amine, as well as potentially of the primary amine and the secondary amine, have a significant effect on the HDN process. Formation of secondary amine from primary amine increases the initial conversion and nitrogen removal rate but appeared to slow down the overall rate of nitrogen removal. The results thus demonstrate how condensation reactions affect amine HDN, which has implications for catalyst design for HDN of renewable feeds containing aliphatic amines.","PeriodicalId":9813,"journal":{"name":"ChemRxiv","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26434/chemrxiv-2024-z1kc3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In this work, the hydrodenitrogenation (HDN) of a primary amine (dodecylamine), a secondary amine (didodecylamine), and a tertiary amine (tridodecylamine) over a Pt/ZrO2 catalyst was compared in a batch reactor. The main product of the amine hydrotreating was dodecane, but significant amounts of secondary amine were also formed as an intermediate during HDN of the primary and the tertiary amine. It was found that the primary amine is the only species for which direct HDN is possible; HDN of the secondary amine thus proceeds through a primary amine intermediate and HDN of the tertiary amine involves formation of secondary amine, which decomposes to primary amine. Consequently, HDN of the tertiary and secondary amines is slower than that of the primary amine. Kinetic modeling indicated that bimolecular condensation reactions of the primary amine, as well as potentially of the primary amine and the secondary amine, have a significant effect on the HDN process. Formation of secondary amine from primary amine increases the initial conversion and nitrogen removal rate but appeared to slow down the overall rate of nitrogen removal. The results thus demonstrate how condensation reactions affect amine HDN, which has implications for catalyst design for HDN of renewable feeds containing aliphatic amines.