摘要
Summary Catalytic dehydrogenation of ethane (EDH) is promising for the utilization of shale gas to produce ethylene, but the current processes mostly exhibit space-time productivity of ethylene lower than 1.5 Kg C2H4 Kg cat −1 h −1 because of the insufficient catalyst activity in the non-oxidative route. We reported a catalyst with isolated cobalt in siliceous zeolite derived from a mechanically assisted spontaneous dispersion. This material can operate as a non-oxidative EDH catalyst at thermodynamically limited conversion levels under rapid gas feeding, resulting in ethylene productivity at 13.4 Kg C2H4 Kg cat −1 h −1 . This result is superior to that of the previous non-noble metal catalysts and even outperforms the precious PtSn/Al 2 O 3 catalyst. The isolated cobalt sites are preserved upon calcination at high temperatures and during EDH operation under harsh conditions, resulting in superior durability in a long reaction period with negligible coke formation.
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