System and process for steam cracking and pfo treatment integrating selective hydrogenation, selective hydrocracking and naphtha reforming

Abstract

A process for treatment of PFO from a steam cracking zone includes selectively hydrogenating PFO or a portion thereof for conversion of polyaromatics compounds contained in the PFO into aromatic compounds with one benzene ring to produce a selectively hydrogenated stream. The selectively hydrogenated stream is selectively hydrocracked for selective ring opening and dealkylation to produce a selectively hydrocracked BTX+ stream. In addition, a naphtha reformer is integrated, so that the selectively hydrocracked BTX+ stream and a reformate stream are separated into BTX compounds. Optionally the PFO is separated into a first stream containing C9+ aromatics compounds with one benzene ring, and a second stream containing C10+ aromatic compounds, whereby the first stream containing C9+ aromatics compounds with one benzene ring is passed to the selective hydrocracking step, and the feed to the selective hydrogenation step comprises all or a portion of the second stream containing C10+ aromatic compounds.

1 . A process for treatment of PFO from a steam cracking zone that produces light olefins and PFO from a steam cracking feed, the process comprising:
 optionally separating the PFO into at least a first stream containing C9+ aromatics compounds with one benzene ring, and a second stream containing C10+ aromatic compounds;   selectively hydrogenating all or a portion of the PFO, or all or a portion of the second stream containing C10+ aromatics compounds, using catalysts and conditions, including hydrogen, effective for conversion of polyaromatics compounds contained in the PFO into aromatic compounds with one benzene ring to produce a selectively hydrogenated stream;   selectively hydrocracking all or a portion of the selectively hydrogenated stream, and optionally all or a portion of the first stream containing C9+ aromatics compounds with one benzene ring, using catalysts and conditions, including hydrogen, effective for selective ring opening and dealkylation to produce a selectively hydrocracked BTX+ stream;   subjecting a naphtha feed to catalytic reforming to produce a reformate stream; and   separating at least a portion of the reformate stream and at least a portion of the selectively hydrocracked BTX+ stream into BTX compounds.   
     
     
         2 . The process as in  claim 1 , wherein the PFO is obtained from steam cracking of treated crude oil or other treated heavy oil feeds, and comprises at least 40 wt % of polyaromatics having three or more aromatic rings including triaromatics, naphtheno-triaromatics, tetraaromatics, penta-aromatics and heavier poly-aromatics including asphaltenes and coke. 
     
     
         3 . The process as in  claim 1 , wherein all or a portion of C20+ polyaromatic compounds are separated from the PFO or from the second stream, prior to selectively hydrogenating all or a portion of the PFO or all or a portion of the second stream containing C10+ aromatics compounds. 
     
     
         4 . The process as in  claim 1 , wherein the PFO is separated into the first stream, the second stream, and a third stream containing C20+ polyaromatic compounds, and wherein the second stream contains C10+ compounds with no less than 2 and up to 6 benzene rings. 
     
     
         5 . The process as in  claim 1 , wherein all or a portion of C9+ aromatics with one benzene ring are selectively hydrogenated with all or a portion of the PFO or all or a portion of the second stream containing C10+ aromatics compounds. 
     
     
         6 . The process as in  claim 1 , wherein the PFO is separated into at least the first stream and the second stream, and wherein all or a portion of the first stream containing C9+ aromatics compounds with one benzene ring bypasses selective hydrogenating and is selectively hydrocracked. 
     
     
         7 . The process as in  claim 1 , wherein the PFO stream or the second stream contains C20+ polyaromatic compounds, and wherein:
 selective hydrogenating occurs in the presence of a selective hydrogenating catalyst, and wherein selective hydrogenating conditions comprise a reaction temperature (° C.) in the range of about 250-500, a reaction pressure (hydrogen partial pressure, kg/cm 2 ) in the range of about 10-70, a hydrogen feed rate (standard liters per liter of hydrocarbon feed, SLt/Lt) in the range of about 30-5000, and a LHSV in the range of about 0.1-20; and   selective hydrocracking occurs in the presence of a selective hydrocracking catalyst, and wherein selective hydrocracking conditions comprise a reaction temperature (° C.) in the range of about 300-550, a reaction pressure (hydrogen partial pressure, kg/cm 2 ) in the range of about 3-30, a hydrogen feed rate (standard liters per liter of hydrocarbon feed, SLt/Lt) in the range of about 1-30, and a LHSV in the range of about 0.1-10.   
     
     
         8 . The process as in  claim 1 , wherein all or a portion of C20+ polyaromatic compounds are removed prior to selective hydrogenation, and wherein:
 selective hydrogenating occurs in the presence of a selective hydrogenating catalyst, and wherein selective hydrogenating conditions comprise a reaction temperature (° C.) in the range of about 250-480, a reaction pressure (hydrogen partial pressure, kg/cm 2 ) in the range of about 10-50, a hydrogen feed rate (standard liters per liter of hydrocarbon feed, SLt/Lt) in the range of about 30-4000, and a LHSV in the range of about 0.1-20; and   selective hydrocracking occurs in the presence of a selective hydrocracking catalyst, and wherein selective hydrocracking conditions comprise a reaction temperature (° C.) in the range of about 300-500, a reaction pressure (hydrogen partial pressure, kg/cm 2 ) in the range of about 3-25, a hydrogen feed rate (standard liters per liter of hydrocarbon feed, SLt/Lt) in the range of about 1-25, and a LHSV in the range of about 0.1-8.   
     
     
         9 . The process as in  claim 1 , wherein light gases from selective hydrogenating and/or selective hydrocracking are treated and one or more LPG streams are recovered, wherein the one or more LPG streams are passed to the steam cracking zone as additional steam cracking feed. 
     
     
         10 . The process as in  claim 1 , wherein the selectively hydrogenated stream is separated into an LPG stream that is treated and passed to the steam cracking zone, and a stream containing one-ring C9+ hydrocarbon compounds that is passed to selective hydrocracking as all or a portion of the selectively hydrogenated stream. 
     
     
         11 . The process as in  claim 1 , wherein separating at least a portion of the selectively hydrocracked stream into BTX compounds further comprises separating C9 aromatic compounds, and wherein the process further comprises transalkylating the separated C9 aromatic compounds to produce a transalkylated effluent containing additional BTX compounds. 
     
     
         12 . The process as in  claim 11 , wherein light gases from transalkylating are treated and one or more LPG streams are recovered, and wherein the one or more LPG streams are passed to the steam cracking zone as additional steam cracking feed. 
     
     
         13 . The process as in  claim 11 , further comprising separating naphtha-range hydrocarbon compounds from the transalkylated effluent prior to separation into BTX compounds, and passing all or a portion of said naphtha-range hydrocarbon compounds to the steam cracking zone as additional steam cracking feed, or wherein all or a portion of said naphtha-range hydrocarbon compounds comprise at least a portion of the naphtha feed to catalytic reforming. 
     
     
         14 . The process as in  claim 11 , further comprising recovering a raffinate stream comprising non-aromatic compounds from the transalkylated effluent, and passing all or a portion of said raffinate stream to the steam cracking zone as additional steam cracking feed. 
     
     
         15 . The process as in  claim 14 , wherein recovering a raffinate stream is by aromatics extraction to separate the selectively hydrocracked stream into the raffinate stream and an extract stream comprising aromatic compounds, and wherein the extract stream is separated into the BTX compounds. 
     
     
         16 . The process as in  claim 1 , wherein separating the selectively hydrocracked stream into BTX compounds further comprises separating C10+ compounds from the selectively hydrocracked stream. 
     
     
         17 . The process as in  claim 16 , wherein at least a portion of the separated C10+ compounds are selectively hydrocracked together with the selectively hydrogenated stream. 
     
     
         18 . The process as in  claim 16 , wherein an initial feed is subjected to treatment upstream of the steam cracking zone, and wherein at least a portion of the separated C10+ compounds are subjected to treatment with the initial feed. 
     
     
         19 . The process as in  claim 1 , further comprising separating naphtha-range hydrocarbon compounds from the selectively hydrogenated stream prior to selective hydrocracking, and passing all or a portion of said naphtha-range hydrocarbon compounds to the steam cracking zone as additional steam cracking feed. 
     
     
         20 . The process as in  claim 1 , further comprising separating naphtha-range hydrocarbon compounds from the selectively hydrocracked stream prior to separation into BTX compounds, and passing all or a portion of said naphtha-range hydrocarbon compounds to the steam cracking zone as additional steam cracking feed. 
     
     
         21 . The process as in  claim 1 , further comprising separating naphtha-range hydrocarbon compounds from the selectively hydrogenated stream prior to selective hydrocracking, wherein all or a portion of said naphtha-range hydrocarbon compounds comprise at least a portion of the naphtha feed to catalytic reforming. 
     
     
         22 . The process as in  claim 1 , further comprising separating naphtha-range hydrocarbon compounds from the selectively hydrocracked stream prior to separation into BTX compounds, wherein all or a portion of said naphtha-range hydrocarbon compounds comprise at least a portion of the naphtha feed to catalytic reforming. 
     
     
         23 . The process as in  claim 1 , further comprising separating at least a portion of the selectively hydrocracked stream into BTX compounds includes recovering a raffinate stream comprising non-aromatic compounds, and passing all or a portion of said raffinate stream to the steam cracking zone as additional steam cracking feed. 
     
     
         24 . The process as in  claim 23 , wherein recovering a raffinate stream is by aromatics extraction to separate the selectively hydrocracked stream into the raffinate stream and an extract stream comprising aromatic compounds, and wherein the extract stream is separated into the BTX compounds. 
     
     
         25 . The process as in  claim 1 , further comprising separating at least a portion of the reformate stream into BTX compounds includes recovering a raffinate stream comprising non-aromatic compounds, and passing all or a portion of said raffinate stream to the steam cracking zone as additional steam cracking feed. 
     
     
         26 . The process as in  claim 25 , wherein recovering a raffinate stream is by aromatics extraction to separate the reformate stream into the raffinate stream and an extract stream comprising aromatic compounds, and wherein the extract stream is separated into the BTX compounds. 
     
     
         27 . A steam cracking process comprising
 steam cracking a steam cracker feed to produce olefins, pyrolysis gasoline and PFO; and   treating the PFO as in the process of  claim 1 .   
     
     
         28 . A system for treatment of PFO from a steam cracking zone that produces at least light olefins and PFO from a steam cracking feed, the system comprising:
 an optional PFO separation zone having one or more inlets in fluid communication with the steam cracking zone, one or more outlets for discharging a fraction of the PFO including C9+ aromatics compounds with one benzene ring, and one or more outlets for discharging a fraction of the PFO including containing C10+ aromatic compounds;   a selective hydrogenation zone having one or more inlets in fluid communication with the steam cracking zone to receive PFO or the second outlet of the PFO separation zone to receive C10+ aromatic compounds from the PFO, and hydrogen, and one or more outlets for discharging reaction effluent including selectively hydrogenated aromatic compounds;   a selective hydrocracking zone having one or more inlets in fluid communication with the one or more outlets of the selective hydrogenation zone, and hydrogen, and one or more outlets for discharging reaction effluent including selectively hydrocracked BTX+ compounds;   a catalytic reforming zone having one or more inlets in fluid communication with a source of naphtha feed and one or more outlets for discharging a reformate stream; and   a BTX splitting zone having one or more inlets in fluid communication with the one or more outlets of the selective hydrocracking zone for discharging reaction effluent including selectively hydrocracked BTX+ compounds, and with the one or more outlets of the catalytic reforming zone for discharging a reformate stream, and one or more outlets for discharging BTX compounds.   
     
     
         29 . The system as in  claim 28 , comprising the PFO separation zone including the one or more outlets for discharging C9+ aromatics compounds with one benzene ring, and the one or more outlets for discharging C10+ aromatic compounds, the PFO separation zone further comprising one or more outlets for discharging a fraction of the PFO including C20+ polyaromatic compounds. 
     
     
         30 - 45 . (canceled)