The effects of reaction conditions on the yield of ethylene and propylene from pentene cracking were investigated in a fixed-bed reactor at 500–750 °C and for a weight hourly space velocity (WHSV) of 15–83 h−1. The total yield of ethylene and propylene reached a maximum (67.8 wt%) at 700 °C and 57 h−1. In order to explore the reaction mechanism at high temperatures, a thermal/catalytic cracking proportion model was established. It was found that the proportion of pentene feed chemically adsorbed with the acid sites and cracked through catalytic cracking was above 88.4%, even at 750 °C. Ethylene and propylene in the products were mainly derived from catalytic cracking rather than thermal cracking at 650–750 °C. In addition, the suitable reaction network for pentene catalytic cracking was deduced and estimated. The results showed that the monomolecular cracking proportion increased from 1% at 500 °C to 95% at 750 °C. The high selectivity of ethylene and propylene at high temperatures was mainly due to the intensification of the monomolecular cracking reaction. After 20 times of regeneration, the acidity and pore structure of the zeolite had hardly changed, and the conversion of pentene remained above 80% at 650 °C.

The effect of reaction temperature and weight hourly space velocity (WHSV) on the reaction of 1-decene cracking to ethylene and propylene over H-ZSM-5 zeolite was investigated. Also, the thermal cracking reaction of 1-decene was studied by cracking over quartz sand as blank. It was observed that 1-decene undergoes a significant thermal cracking reaction above 600 °C over quartz sand. In the range of 500−750 °C, the conversion remained above 99% for 1-decene cracking over H-ZSM-5, and the catalytic cracking dominated even at 750 °C. With the increase in temperature, the yields of ethylene and propylene gradually increased, and the yields of alkanes and aromatics also increased. The low WHSV was favorable for the yield of light olefins. With the increase of the WHSV, the yields of ethylene and propylene decrease. However, at low WHSV, secondary reactions were accelerated, and the yields of alkanes and aromatics increased significantly. In addition, the possible main and side reaction routes of the 1-decene cracking reaction were proposed based on product distribution.

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