Abstract
The methanol-to-hydrocarbons (MTH) reaction was studied over a moderately acidic zeotype material, H-SAPO-5, at 350–450°C and with WHSV=0.3–5h−1. C3–C5 alkenes were the main products of reaction, followed by C6+ aliphatics. Conversion-selectivity plots from experiments conducted at various contact times revealed that coking did not influence product selectivity significantly. Steady-state isotope transient experiments (12CH3OH//13CH3OH) were performed at 450°C. 13C incorporation was more rapid in the alkene products than in the polymethylated benzene molecules that were retained inside the catalyst after testing, suggesting that polymethylbenzenes contribute only to a minor extent to alkene formation in H-SAPO-5. Co-feed studies of methanol and benzene at 350°C revealed that benzene shifts the product selectivity towards ethene and aromatic products. Co-feeding 13CH3OH and benzene at 250°C, giving <2% conversion of both reactants, indicated that polymethylbenzenes, when present in excessive amounts, may contribute to ethene and propene, but not to C4+ alkene, formation. Furthermore, the isotopic labelling pattern of ethene provided the first direct experimental evidence for ethene formation by a paring-type reaction from polymethylated benzene intermediates. Overall, the results obtained in this study suggest that a lower acid strength promotes an alkene-mediated MTH reaction mechanism, and that acid strength is therefore an important design parameter for selectivity optimisation in zeotype catalysis.
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