The current commercial process for producing ethylene is steam cracking of ethane. Ethane is heated until it pyrolyzes into ethylene. This process consumes large amounts of methane, operates at 800°C and has residence times of about one second. It also forms significant quantities of solid carbon, or coke, which leads to steam addition to inhibit its formation.; In comparison, our group has investigated partial oxidation of ethane to ethylene using a millisecond contact time reactor operating at about 1000°C. By adding oxygen and using a Pt-coated alumina foam monolith in a quartz tube, combustion reactions provide sufficient energy to crack the remaining ethane into ethylene, without coking. Adding Sn improves results, and adding H 2 to the feed increases selectivity even more.; However, time dependence studies show a slow decrease in activity, which occurs due to Sn loss. To counter this, SnCl2 solution is added in-situ by dripping it onto the upstream catalyst face, thus regenerating it without reactor shutdown. This on-line addition also allows for screening of various metals and examination of the dynamic behavior of the reactor system.; On-line addition of Pt creates superior results to catalyst preparation by incipient wetness, especially when combined with H2 addition. This may be since on-line addition keeps almost all Pt on the front face of the monolith, and SEM results indicate on-line addition creates rougher Pt particles than those formed through incipient wetness. Continued work with this apparatus may lead to a better understanding of the mechanism of ethylene formation. |