Thermally stable imidazole/heteropoly acid composite as a heterogeneous catalyst for m-xylene ammoxidation

Ammoxidation of m -xylene is evaluated in the presence of a customized heteropoly acid catalyst as an imidazole/molybdovanadophosphoric acid (imidazole/PMoV). Imidazole is employed to maintain its heterogeneous phase during the ammoxidation reaction and to provide the thermal stability of PMoV with...

Full description

Saved in:
Bibliographic Details
Published inResearch on chemical intermediates Vol. 47; no. 1; pp. 287 - 302
Main Authors Jeon, Yukwon, Lee, Chanmin, Lee, Gicheon, Kwon, Ohchan, Kim, Jinsol, Park, Sang Sun, Oh, Kyeongseok, Shul, Yong-Gun
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.01.2021
Springer Nature B.V
Subjects
Online AccessGet full text
ISSN0922-6168
1568-5675
DOI10.1007/s11164-020-04342-1

Cover

More Information
Summary:Ammoxidation of m -xylene is evaluated in the presence of a customized heteropoly acid catalyst as an imidazole/molybdovanadophosphoric acid (imidazole/PMoV). Imidazole is employed to maintain its heterogeneous phase during the ammoxidation reaction and to provide the thermal stability of PMoV with the expectation that imidazole can generate strong electronic interactions with terminal molybdenum-oxygen on PMoV. The characterizations of the prepared catalysts are performed using SEM–EDX, XRD, FT-IR, Raman, XPS, and TGA to prove the physical and chemical changes by incorporating imidazole to PMoV, respectively. Also, the thermal stability of the developed catalyst is confirmed by the means of heat treatment test at relatively high temperature. The composite catalyst, imidazole/PMoV, shows an excellent conversion rate of over 98% with high selectivity of isophthalonitrile in m -xylene ammoxidation. Moreover, while the imidazole-free PMoV catalyst is deactivated and washed out during the reaction, the catalyst durability of the imidazole/PMoV is preserved without significant activity loss after 5 reaction cycles at 380 °C.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ISSN:0922-6168
1568-5675
DOI:10.1007/s11164-020-04342-1