Methods of treating hydroconversion catalysts used for cracking of hydrocarbons are described. A method can include mixing an inactive hydroconversion catalyst with a solid hydrocarbon containing material having a melting point of 50° C. or greater. The inactive hydroconversion catalyst/solid hydrocarbon containing material mixture can be contacted with a gaseous stream that includes hydrogen (H.sub.2) and a sulfur-containing compound under conditions sufficient to sulfide the catalyst and carbonize at least a portion of the hydrocarbon containing material on the sulfided catalyst to obtain a treated sulfided hydroconversion catalyst.

Methods of treating hydroconversion catalysts used for cracking of hydrocarbons are described. A method can include mixing an inactive hydroconversion catalyst with a solid hydrocarbon containing material having a melting point of 50° C. or greater. The inactive hydroconversion catalyst/solid hydrocarbon containing material mixture can be contacted with a gaseous stream that includes hydrogen (H.sub.2) and a sulfur-containing compound under conditions sufficient to sulfide the catalyst and carbonize at least a portion of the hydrocarbon containing material on the sulfided catalyst to obtain a treated sulfided hydroconversion catalyst.

Disclosed are a catalyst pre-hydrocarbon-pooling method and a pre-hydrocarbon-pooling device, relating to the technical field of preparation of low carbon olefins. A regenerated catalyst enters a pre-hydrocarbon-pooling reactor, and a pre-hydrocarbon-pooling reaction occurs between the regenerated catalyst and an activation medium to form “hydrocarbon pool” active species. “Pre-hydrocarbon-pooling” treatment is performed on the regenerated catalyst by providing a pre-hydrocarbon-pooling device, so that the regenerated catalyst forms the “hydrocarbon pooled” active species and carbon deposition before entering into an oxygenate conversion reactor, by way of which “hydrocarbon pool” active species distribution and coke distribution of the catalyst in the conversion reactor are improved. This shortens or eliminates a reaction “induction period” and improves the catalytic activity and selectivity of the regenerated catalyst for a reaction of an oxygenate to low-carbon olefins.

Disclosed are a catalyst pre-hydrocarbon-pooling method and a pre-hydrocarbon-pooling device, relating to the technical field of preparation of low carbon olefins. A regenerated catalyst enters a pre-hydrocarbon-pooling reactor, and a pre-hydrocarbon-pooling reaction occurs between the regenerated catalyst and an activation medium to form “hydrocarbon pool” active species. “Pre-hydrocarbon-pooling” treatment is performed on the regenerated catalyst by providing a pre-hydrocarbon-pooling device, so that the regenerated catalyst forms the “hydrocarbon pooled” active species and carbon deposition before entering into an oxygenate conversion reactor, by way of which “hydrocarbon pool” active species distribution and coke distribution of the catalyst in the conversion reactor are improved. This shortens or eliminates a reaction “induction period” and improves the catalytic activity and selectivity of the regenerated catalyst for a reaction of an oxygenate to low-carbon olefins.

A regeneration method for a benzene alkylation solid acid catalyst, comprising: purging the solid acid catalyst in a reactor with a gas; continuously injecting n-hexane at a feed port of the reactor and heating the n-hexane to wash the solid acid catalyst, and discharging the n-hexane entraining benzene alkylation reaction residues from a discharge port of the reactor; and stopping injecting n-hexane, cleaning off a liquid in the reactor by purging with the gas, and cooling the reactor. In the regeneration method of the present disclosure, the regeneration liquid used is n-hexane, which can increase the solubility of the residues in channels and enhance the regeneration effect. Meanwhile, permanent damage to the channel structure of the catalyst caused by carbon burning regeneration can be avoided, thereby prolonging the lifetime of the catalyst.

A regeneration method for a benzene alkylation solid acid catalyst, comprising: purging the solid acid catalyst in a reactor with a gas; continuously injecting n-hexane at a feed port of the reactor and heating the n-hexane to wash the solid acid catalyst, and discharging the n-hexane entraining benzene alkylation reaction residues from a discharge port of the reactor; and stopping injecting n-hexane, cleaning off a liquid in the reactor by purging with the gas, and cooling the reactor. In the regeneration method of the present disclosure, the regeneration liquid used is n-hexane, which can increase the solubility of the residues in channels and enhance the regeneration effect. Meanwhile, permanent damage to the channel structure of the catalyst caused by carbon burning regeneration can be avoided, thereby prolonging the lifetime of the catalyst.

Embodiments provide a method for determining a chloride content of an alumina-based catalyst used for catalytic reforming. The method includes the step of combining nitric acid, isopropanol, and the alumina-based catalyst such that the alumina-based catalyst is dissolved in the nitric acid and the isopropanol to form a homogenized mixture. The alumina-based catalyst include chloride. The method includes the step of taking a conductivity measurement of the homogenized mixture using a pair of electrodes. The method includes the step of introducing a titrant solution comprising silver nitrate to the homogenized mixture such that a precipitate of silver chloride is formed. The method includes the step of determining a chloride concentration of the homogenized mixture based on the conductivity measurement of the homogenized mixture. The method includes the step of determining the chloride content of the alumina-based catalyst based on the chloride concentration of the homogenized mixture.

Embodiments provide a method for determining a chloride content of an alumina-based catalyst used for catalytic reforming. The method includes the step of combining nitric acid, isopropanol, and the alumina-based catalyst such that the alumina-based catalyst is dissolved in the nitric acid and the isopropanol to form a homogenized mixture. The alumina-based catalyst include chloride. The method includes the step of taking a conductivity measurement of the homogenized mixture using a pair of electrodes. The method includes the step of introducing a titrant solution comprising silver nitrate to the homogenized mixture such that a precipitate of silver chloride is formed. The method includes the step of determining a chloride concentration of the homogenized mixture based on the conductivity measurement of the homogenized mixture. The method includes the step of determining the chloride content of the alumina-based catalyst based on the chloride concentration of the homogenized mixture.

A catalytic upgrading process includes introducing a feed comprising crude oil to a steam cracking unit, thereby producing pyrolysis fuel oil (PFO). The PFO is introduced to a first catalytic depolyaromatization reactor to remove polyaromatics from the feed, thereby producing polyaromatics adsorbed to the catalyst and depolyaromatized PFO. The depolyaromatized PFO is introduced to a hydrocracking unit. The resulting benzene-toluene-xylenes (BTX) and liquid petroleum gas (LPG) are separated, and the BTX is introduced to a BTX complex to produce refined BTX. The LPG can then be introduced to the steam cracking unit. After depolyaromatization, a wash solvent is introduced into the first catalytic depolyaromatization reactor to remove the polyaromatics, regenerate the catalyst, and produce a mixture comprising the wash solvent and the polyaromatics. The wash solvent is separated from the polyaromatics.

The invention is concerned with the oligomerization of supercritical ethene. An essential aspect of the invention is that of mixing ethene with an inert medium and setting the conditions in the reaction such that both ethene and inert medium are supercritical. This is because the solubility for ethene in the inert medium is greater in the supercritical state, such that more ethene is dissolved in the supercritical inert medium than in a liquid solvent. The process regime in the supercritical state therefore enables the use of a much higher proportion of ethene in a homogeneous mixture of ethene and inert medium than is possible on the basis of the thermodynamic solubility restriction in a purely liquid hydrocarbon stream. In this way, the space-time yield is distinctly enhanced. Since a greater amount of ethene can be passed into the reactor, it is possible as a result to better exploit the apparatus volume compared to a liquid phase process. The inert medium used may, for example, be isobutane.