The present disclosure relates to novel metal-organic frameworks (MOFs) comprising tetratopic ligands with small pore apertures. The present disclosure further relates to methods of utilizing the MOFs of the disclosure to separate hydrocarbons through adsorptive processes.

The present disclosure relates to novel metal-organic frameworks (MOFs) comprising tetratopic ligands with small pore apertures. The present disclosure further relates to methods of utilizing the MOFs of the disclosure to separate hydrocarbons through adsorptive processes.

Methods for cracking a hydrocarbon feed stream include contacting a hydrocarbon feed stream with a catalyst system in a catalytic cracking unit having a flowing gas stream to obtain a cracking product containing light olefins. The catalyst system includes at least a base catalyst. The base catalyst includes a pentasil zeolite. The pentasil zeolite includes from 0.01% to 5% by mass lithium atoms, as calculated on an oxide basis, based on the total mass of the pentasil zeolite. The flowing gas stream comprises hydrogen and, optionally, at least one additional carrier gas.

Methods for cracking a hydrocarbon feed stream include contacting a hydrocarbon feed stream with a catalyst system in a catalytic cracking unit having a flowing gas stream to obtain a cracking product containing light olefins. The catalyst system includes at least a base catalyst. The base catalyst includes a pentasil zeolite. The pentasil zeolite includes from 0.01% to 5% by mass lithium atoms, as calculated on an oxide basis, based on the total mass of the pentasil zeolite. The flowing gas stream comprises hydrogen and, optionally, at least one additional carrier gas.

A method of recovery of rich gas where the rich gas is a hydrocarbon gas comprising less than 50 mole % methane is disclosed. The method comprises the steps of gathering the low pressure gas, compressing the gathered gas, cooling the compressed gas in a condenser so that a portion of the compressed gas condenses to form a liquefied gas and liquefied gas vapour in the condenser, and discharging the liquefied gas and liquefied gas vapour from the condenser, in which the cooling of the compressed gas is performed using at least one heat exchanger (40).

A method of recovery of rich gas where the rich gas is a hydrocarbon gas comprising less than 50 mole % methane is disclosed. The method comprises the steps of gathering the low pressure gas, compressing the gathered gas, cooling the compressed gas in a condenser so that a portion of the compressed gas condenses to form a liquefied gas and liquefied gas vapour in the condenser, and discharging the liquefied gas and liquefied gas vapour from the condenser, in which the cooling of the compressed gas is performed using at least one heat exchanger (40).

A process can be used for purifying a hydrocarbon stream containing at least Cx alkanes, Cx olefins, low boilers such as Cx−1 hydrocarbons, and high boilers such as Cx+1 hydrocarbons, with x=3 or 4. The process involves separating off low boilers and separating off high boilers, wherein the separating-off of high boilers is performed in the presence of hydrogen and hence a hydrogenation of the olefins present takes place.

A process can be used for purifying a hydrocarbon stream containing at least Cx alkanes, Cx olefins, low boilers such as Cx−1 hydrocarbons, and high boilers such as Cx+1 hydrocarbons, with x=3 or 4. The process involves separating off low boilers and separating off high boilers, wherein the separating-off of high boilers is performed in the presence of hydrogen and hence a hydrogenation of the olefins present takes place.

A carbon molecular sieve (CMS) membrane having improved separation characteristics for separating olefins from their corresponding paraffins is comprised of carbon with at most trace amounts of sulfur and a group 13 metal. The CMS membrane may be made by pyrolyzing a precursor polymer devoid of sulfur in which the precursor polymer has had a group 13 metal incorporated into it, wherein the metal is in a reduced state. The pyrolyzing for the precursor having the group 13 metal incorporated into it is performed in a nonoxidizing atmosphere and at a heating rate and temperature such that the metal in a reduced state (e.g., covalently bonded to carbon or nitrogen or in the metal state).

A carbon molecular sieve (CMS) membrane having improved separation characteristics for separating olefins from their corresponding paraffins is comprised of carbon with at most trace amounts of sulfur and a group 13 metal. The CMS membrane may be made by pyrolyzing a precursor polymer devoid of sulfur in which the precursor polymer has had a group 13 metal incorporated into it, wherein the metal is in a reduced state. The pyrolyzing for the precursor having the group 13 metal incorporated into it is performed in a nonoxidizing atmosphere and at a heating rate and temperature such that the metal in a reduced state (e.g., covalently bonded to carbon or nitrogen or in the metal state).