词条 | Coking |
释义 |
A simplified equation for coking is shown in the case of ethylene: 3 C2H4 → 2 C ("coke") + 2 C2H6 A more realistic but complex view involves the alkylation of an aromatic ring of a coke nucleus. Acidic catalysts are thus especially prone to coking because they are effective at generating carbocations (i.e., alkylating agents). Coking is one of several mechanisms for the deactivation of a heterogeneous catalyst. Other mechanisms include sintering, poisoning, and solid-state transformation of the catalyst.[2][3] References1. ^{{cite journal|title=“Coking” of zeolites during methanol conversion: Basic reactions of the MTO-, MTP- and MTG processes|journal=Catalysis Today|volume=154|pages=183-194|doi=10.1016/j.cattod.2010.05.012|author=H. Schultz}} 2. ^{{cite journal|title=Catalyst Deactivation|authors=Forzatti, P.; Lietti, L.|journal=Catalysis Today|year=1999|volume=52|pages=165-181|doi=10.1016/S0920-5861(99)00074-7}} 3. ^{{cite journal|last1=Bartholomew|first1=Calvin H|title=Mechanisms of Catalyst Deactivation|journal=Applied Catalysis A: General|volume=212|issue=1–2|pages=17–60|doi=10.1016/S0926-860X(00)00843-7|year=2001}} 2 : Coking works|Catalysis |
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