Cruz-Cabeza Aurora J, Esquivel Dolores, Jiménez-Sanchidrián César, Romero-Salguero Francisco J
Departamento de Química Orgánica, Instituto Universitario de Investigación en Química Fina y Nanoquímica (IUIQFN), Universidad de Córdoba, Campus de Rabanales, Edificio Marie Curie, Ctra. Nnal. IV, km 396, Córdoba 14014, Spain.
Materials (Basel). 2012 Jan 5;5(1):121-134. doi: 10.3390/ma5010121.
Various metal-β zeolites have been synthesized under similar ion-exchange conditions. During the exchange process, the nature and acid strength of the used cations modified the composition and textural properties as well as the Brönsted and Lewis acidity of the final materials. Zeolites exchanged with divalent cations showed a clear decrease of their surface Brönsted acidity and an increase of their Lewis acidity. All materials were active as catalysts for the transformation of acetone into hydrocarbons. Although the protonic zeolite was the most active in the acetone conversion (96.8% conversion), the metal-exchanged zeolites showed varied selectivities towards different products of the reaction. In particular, we found the Cu-β to have a considerable selectivity towards the production of isobutene from acetone (over 31% yield compared to 7.5% of the protonic zeolite). We propose different reactions mechanisms in order to explain the final product distributions.
在相似的离子交换条件下合成了各种金属-β沸石。在交换过程中,所用阳离子的性质和酸强度改变了最终材料的组成、织构性质以及布朗斯特和路易斯酸度。与二价阳离子交换的沸石其表面布朗斯特酸度明显降低,路易斯酸度增加。所有材料作为丙酮转化为烃类的催化剂均具有活性。尽管质子型沸石在丙酮转化中活性最高(转化率为96.8%),但金属交换沸石对反应的不同产物表现出不同的选择性。特别是,我们发现Cu-β对由丙酮生产异丁烯具有相当高的选择性(产率超过31%,相比之下质子型沸石为7.5%)。我们提出了不同的反应机理以解释最终产物分布。