Method for preparing isooctane by isobutene superposition-hydrogenation
A technology for isobutene and isooctane, which is applied in the field of isobutene superposition-hydrogenation to prepare isooctane, can solve the problem of not involving isooctane and the like, and achieve the effects of shortened residence time, long service life of catalyst and simplified process
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Embodiment 1
[0049] The styrene-divinylbenzene macroporous sulfonic acid resin catalyst of loading 50mL load Pd in the fixed-bed reactor, the dry basis acid amount of this catalyst is 3.5mol H + / kg, the dry basis Pd content is 0.7wt%. The specific surface area of the catalyst is 36m 2 / g, the pore volume is 0.22mL / g, and the average pore diameter is 27nm. The catalyst was activated for 8 hours at a temperature of 110 °C, a pressure of 0.5 MPa, and a hydrogen flow rate of 4 mL / (min·mL catalyst) to complete the reduction and activation treatment. The raw material was mixed hydrocarbons with a weight ratio of isooctane / isobutene of 5:1. Based on the weight of the raw material, add 6wt% tetrahydrofuran to the raw material as a dimer selectivity regulator, mix it evenly, and mix it with the hydrogen flow, at a temperature of 80°C, a pressure of 0.8 MPa, and a hydrogen / isobutene molar ratio of 2.0 and the volumetric space velocity of the fresh raw material is 3.0h -1 Under certain reacti...
Embodiment 2
[0051] Use "methacrylic anhydride-methacrylic acid methanol macroporous sulfonic acid resin catalyst" to replace the "styrene-divinylbenzene macroporous sulfonic acid resin catalyst" in Example 1, and the remaining reaction conditions are the same as in Example 1 to start the reaction . The specific reaction results are shown in Table 1.
Embodiment 3
[0053] The "bisphenol-methacrylic acid epoxy macroporous sulfonic acid resin catalyst" was used to replace the "styrene-divinylbenzene macroporous sulfonic acid resin catalyst" in Example 1, and the rest of the reaction conditions were the same as in Example 1 to start the reaction. The specific reaction results are shown in Table 1.
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