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Effect of the nature of rhodium catalyst supports on initiation of H _2 production during n-butane oxidative reforming at room temperature

机译:铑催化剂载体性质对室温下正丁烷氧化重整过程中H _2生成的影响

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摘要

Three rhodium catalysts supported on rare earth oxides with redox properties, Rh/CeO _2, Rh/Pr _6O _(11), and Rh/Tb _4O _7, were tested for their ability to trigger oxidative reforming of n-butane at room temperature. Only Rh/CeO _2 triggered the oxidative reforming, owing to the heat generated by the spontaneous oxidation of the CeO _(2-x) species produced by prior reduction of the supported catalyst with H _2. Although the three rare earth oxides were reduced to CeO _(1.91), Pr _2O _3, and Tb _2O _3, respectively, by H _2 at ≥873 K, CeO _(1.91) was the only reduced oxide that was oxidized upon exposure to O _2 at room temperature. These results indicate that the ability of the reduced oxide support to undergo oxidation at room temperature was crucial for triggering oxidative reforming of n-butane at room temperature.
机译:测试了三种负载在具有氧化还原特性的稀土氧化物上的铑催化剂Rh / CeO _2,Rh / Pr _6O _(11)和Rh / Tb _4O _7在室温下引发正丁烷氧化重整的能力。由于由预先用H _2还原负载型催化剂而产生的CeO _(2-x)物种自发氧化产生的热量,只有Rh / CeO _2触发了氧化重整。尽管这三种稀土氧化物在≥873 K时被H _2分别还原为CeO _(1.91),Pr _2O _3和Tb _2O _3,但CeO _(1.91)是唯一暴露于金属氧化物中被氧化的还原氧化物。室温下为O _2。这些结果表明,还原的氧化物载体在室温下进行氧化的能力对于在室温下引发正丁烷的氧化重整至关重要。

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