Abstract
A highly dealuminated H-mordenite used for the isopropylation of biphenyl contained deposited coke and encapsulated products in its pores. Coke deposition occurred rapidly in the early stage, and the amount of encapsulated products was constant during the reaction. Propylene oligomerization began rapidly after the conversion of biphenyl reached 40 %, and increased up to ca. 11 % in consumed propylene. These results show that deposited coke was mainly formed from biphenyl and its alkylates, and not from propylene
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