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Template-controlled acidity and catalytic activity of ferrierite crystals

机译:模板控制的镁碱沸石晶体的酸度和催化活性

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摘要

A synthesis strategy to tailor the acid sites location in ferrierite crystals has been developed. The zeolite catalysts were synthesised in fluoride medium using different combinations of organic structure directing agents (SDAs) in the absence of inorganic cations. Therefore, the negative charge associated to the incorporation of aluminium to the framework was compensated exclusively by the positive charge of the organic SDAs. In this way, Al sitting in the zeolite framework was driven by the specific location of the different SDA molecules within the zeolite void volume. Following this synthesis strategy, it has been found that the distribution of strongly acidic hydroxyl groups in the proton form of the zeolites obtained after removal of the organic templates was dependent on the combination of organic molecules used as SDAs. Moreover, the catalytic activity of the zeolites in m-xylene and 1-butene isomerisation increased as the relative population of strong Br?nsted acid groups in sterically constrained sites inside the ferrierite cavity decreased.
机译:已经开发出一种合成策略,以调整镁碱沸石晶体中的酸位点位置。在不存在无机阳离子的情况下,使用有机结构定向剂(​​SDA)的不同组合在氟化物介质中合成了沸石催化剂。因此,与铝结合到框架相关的负电荷仅由有机SDA的正电荷补偿。以这种方式,位于沸石骨架中的Al是由沸石空隙体积内不同SDA分子的特定位置驱动的。按照这种合成策略,已经发现在除去有机模板后获得的沸石的质子形式中的强酸性羟基的分布取决于用作SDA的有机分子的组合。此外,随着镁碱沸石腔内空间受限位点中强布朗斯台德酸基团的相对数量减少,沸石在间二甲苯和1-丁烯异构化中的催化活性增加。

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