US3923921A - Naphtha steam-cracking quench process - Google Patents

Naphtha steam-cracking quench process Download PDF

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US3923921A
US3923921A US365052A US36505273A US3923921A US 3923921 A US3923921 A US 3923921A US 365052 A US365052 A US 365052A US 36505273 A US36505273 A US 36505273A US 3923921 A US3923921 A US 3923921A
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steam
quench
effluent
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quench tower
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Walter C Kohfeldt
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/002Cooling of cracked gases
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D51/00Auxiliary pretreatment of gases or vapours to be cleaned
    • B01D51/10Conditioning the gas to be cleaned
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S585/00Chemistry of hydrocarbon compounds
    • Y10S585/949Miscellaneous considerations
    • Y10S585/95Prevention or removal of corrosion or solid deposits

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  • ABSTRACT In quenching the hot gaseous effluent from a naphtha steam-cracking operation employing transfer line heat exchangers, improved heat recovery is obtained by recycling a high boiling fraction, i.e., filtered steamcracked tar bottoms, to the quench point in addition to quenching with a steam-cracked gas oil fraction recovered from the quench tower.
  • the use of the high boiling fraction, i.e., tar bottoms, in conjunction with the steam-cracked gas oil fraction to quench the effluent which has previously passed through a transfer line heat exchanger maintains the temperature of the effluent passing to the quench tower in the range of from about 500 to about 650F. while insuring a liquid phase on the walls of the transfer line to prevent fouling, and thus allows additional high-level heat recovery in the quench tower.
  • This invention relates to a method of quenching a hot gaseous effluent of steam-cracked naphtha products being transferred from a cracking coil outlet into a quench tower for separation of the products into fractions. More particularly, this invention relates to an improved steam-cracking quench process wherein the ef fluent from the furnace is first passed through a heat exchanging zone and thereafter quenched with a circulating quench oil fraction, i.e., steam-cracked gas oil recovered as a distillate fraction from the quenching and fractionationzone.
  • a circulating quench oil fraction i.e., steam-cracked gas oil recovered as a distillate fraction from the quenching and fractionationzone.
  • quench tower i.e., quench tower and with a high boiling fraction such as filtered steam cracker tar bottoms recycled from the quench tower to the quench point
  • a novel quench system allows the temperature of the effluent passing to the quench tower to be maintained at a temperature in the range of from about 500 to about 650F. while at the same time maintaining a liquid phase on the wall of the transfer line or order to prevent fouling thereof. Accordingly, high-level heat recovery is obtained by first passing the effluent from the furnace through a transfer line heat exchanger and, after employing the quench system heretofore described, passing the effluent at a preferred temperature in the range of from about 525 to about 600F.
  • the effluent is quenched with a steam-cracked oil distillate fraction recovered from the quench tower and recycled to the quench point.
  • This fraction lowers the temperature to a range of from about 5 to about'600F., permitting substantial recovery of high-level heat, i.e., recovering X BTU per hour as 125 to about 145 psig steam generation in the quench tower equipment.
  • one or more transfer line heat exchangers are employed to initially cool the effluent from the furnace and to recover a substantial amount of heat, i.e., about 0.85 X BTU/hr.
  • a high-boiling fraction such as filtered steam-cracked tar bottoms recovered from the quench tower is recycled along with a steam-cracked oil distillate fraction recovered from the quench tower to the quench point in order to maintain the temperature of the effluent in the transfer line in the range of from about 525F. to about 600F. while at the same time maintaining a liquid phase on the wall of the transfer line passing to the quench tower in order to recover 0.85 X BTU/hr. as about 1800 psig steam and 0.15 X BTU(hr. as to about psig steam.
  • the instant quenching scheme allows the effluent to pass into the quench tower at a sufficient temperature to provide for substantial high-level heat recovery in the quench tower equipment and at the same time provides a liquid phase on the wall of the transfer line passing from the quench point to the quench tower in order to prevent plugging and fouling therein.
  • a hydrocarbon feedstock 1 is passed by line 2 into a preheat and cracking coil located within the cracking furnace 3, wherein the cracking coil is exposed to high intensity radiant heat.
  • the preferred hydrocarbon feedstock is a naphtha fraction containing principally C,-,C saturated aliphatic hydrocarbons, i.e., paraffins or naphthenes, boiling principally in the range from about 100 to 350F.
  • the feedstock may have a somewhat narrower boiling range, e.g., in the range of from about 100 to about F.
  • a suitable proportion of steam passing by way of line 4 is added to the hydrocarbon feed to make the resulting cracking mixture contain from about 40 to about 65 mole steam, thus substantially lowering the partial pressure of the hydrocarbons.
  • the naphtha hydrocarbons mixed with steam are heated to an outlet temperature in the range of from about l450 to about 1650F., preferably in the range of from about 1500 to loO0F.
  • the total pressure of the cracked reaction mixture is in the range of from about 1.5 to 3 atmospheres, and preferably less than 30 pounds per square inch absolute.
  • the residence time of the cracked reaction mixture of steam and hydrocarbons in the cracking coil is in the range of from about 0.] to about 0.6 seconds, and more preferably for about 0.3 to about 0.5 seconds.
  • the cracked reaction of products is transferred by way of line 5 to transfer line heat exchanger 6.
  • the temperature (cot) of the reaction products leaving the outlet of the coil is in the range of from about l450 to 1650F., and more preferably from about l500 to 1600F.
  • the effluent After passing through heat exchanger 6, the effluent is cooled to a temperature below about 850F., and preferably to a temperature in the range of from about 650 to about 8l5F.
  • the heat recovered by the effluent passing through the heat exchanger generates steam in the range of from about 600 to about 1800 psig steam, preferably from about 1400 to 1800 psig.
  • the effluent having been quenched in the transfer line heat exchanger to a temperature in the range from about 650 to about 815F. is passed by way ofline 7 to the quench tower 8.
  • a steam-cracked oil fraction is withdrawn from the lower portion of the quench tower 8 at a temperature in the range of from about 450 to 550F. through line 9 and is passed by pump 10 through line 1] for cooling in heat exchanger 12.
  • Heat recovered in heat exchanger 12 generates steam in the range of from about 100 to about 150 psig.
  • the cooled oil distillate fraction leaving the heat exchanger 12 at a tern perature in the range of from about 350 to about 400 F. through line 13 becomes divided into two streams.
  • One stream of the cooled oil distillate fraction is passed through line 14 for further cooling in the second heat exchanging zone 15.
  • Heat recovered in heat exchanger 15 generates steam in the range of from about 10 to about 30 psig.
  • the oil distillate cooled in the heat exchanger 15 is passed by line 16 into the top section of the quench tower for partial cooling of the vapors flowing upwardly through quench tower 8.
  • a sufficient amount of the oil distillate having a temperature in the range of from about 350 to about 400F. is passed from line 13 into line 14 and is injected at one or more points into line 7 to effect the lowering of the temperature in the effluent passing from the transfer line heat exchanger to a temperature in the range of from about 525 to about 600F.
  • the steam-cracked oil distillate fraction which is injected into line 7 by way of line 14 has a preferred boiling range of from about 350 to about 750F., and more preferably from about 450 to about 650F.
  • the flow rate of the oil distillate from line 14 into line 7 is in the range of from about 0.3 to about 0.8 parts by weight of the oil fraction per one part by weight of the effluent from the furnace, the oil fraction having a temperature in the range of from about 350 to about 400F.
  • the bottoms fraction is withdrawn from quench tower 8 at a temperature in the range of from about 525 to about 600F. through line 17 and is passed by pump 18 through line 19 to a filter 20.
  • the bottoms product recovered from quench tower 8 to line 7 comprises steam-cracked tar bottoms.
  • the coke and other carbonaceous particles present in said product are removed in the filter 20 and tower bottoms pass by way of line 21 for cooling in heat exchanger 22.
  • a sufficient amount of the cooled high-boiling fraction is recovered from heat exchanger 22 and passed by way of line 23 through line 24- and injected into line 7 at one or more points in order to maintain a liquid phase on the wall of line 7.
  • the boiling point'of the material i.e..
  • steamcracked tar bottoms passing by way of line 24 is in the range of from about 550 to about 800F.
  • the flow rate from line 24 into line 7 is in the range of from about 0.01 to about 0.03 parts by weight of the bottoms product passing by way of line 24 per one part by weight of the sum of the effluent and oil distillate, the temperature of the high-boiling material passing by way of line 24 being in the range of about 130 to about 250F.
  • the mixture of the cracked products and the steamcracked oil fraction and high-boiling bottoms fraction passing by way of line 7 is preferably introduced into the bottom of the quench tower at a temperature in the range from about 525 to 600F.
  • gaseous vapors containing steam-cracked hydrocarbon products boiling below about 450F., steam, and hydrogen is taken overhead from the tower 8 through line 25.
  • This gaseous stream is passed by way of line 25 into condenser 26 which is operated at a sufficiently low temperature to condense out water and hydrocarbons having more than about 7 carbon atoms per molecule.
  • the condensate is then passed by way of line 27 into a separation tank 28 wherein the liquid condensate is settled so that a lower water layer can be withdrawn to line 29 and condensed oil can be withdrawn from an upper liquid layer through line 30.
  • Uncondensed gaseous hydrocarbon products containing principally oletins and diolefins having up to about 6 carbon atoms per molecule are withdrawn from vessel 28 to line 33 to be subjected to light ends processing i.e., recover ethylene, propylene, butenes, butadienes and the like.
  • a portion of the condensed oil withdrawn from settling drum 28 by way of line 30 is passed by way of line 31 into the upper portion of quench tower 8 to form a reflux medium for the top of the tower.
  • the interior of quench tower 8 is equipped with plates 32 for obtaining contact between the liquid and vapor but allowing for the fast flow of materials.
  • the necessary cooling is obtained in the upper part of the quench tower 8 by the injection of the cooled oil distillate fraction introduced to the tower by way of line 16 and by introducing the condensed oil introduced by way of line 31.
  • Each of these streams is introduced in suitable amounts and at the proper temperatures at several space points in order to obtain the optimum cooling and fractionation.
  • the temperature of the vapors at EXAMPLE While various virgin naphtha fractions may be employed as the feedstocks of the instant invention, a preferred feed contains hydrocarbons boiling principally in the range of to 300F. The feed is cracked at temperatures of about 1500F.
  • the cracked products leave the outlet coil at about 1500F. and are then introduced into the transfer line heat exchanger.
  • the cracked products are recovered from the transfer line heat exchanger at a temperature in the range of from about 650F. to 8l5F.
  • the effluent is then quenched by a steam-cracked gas oil distillate fraction being removed from the lower section of the quench tower, and after passing through a heat exchanger is injected into the quench point or points at a temperature of about 375F., the proportion of steamcracked oil quench being about 0.5 times the weight of the admixed hydrocarbon products which are being quenched.
  • a steam-cracked tar bottoms fraction having a boiling point of about 750F. is removed from the bottom of the quench tower, and after being filtered and passed through a heat exchanger such that the temperature of the tar fraction is about 200F., is injected at said temperature into the quench points in the transfer line, the proportion of tar bottoms quench oil being 0.02 times the weight of the admixed cracked hydrocarbon products and steamcracked oil quench which are passing in the transfer line to the quench tower.
  • the amount of steam-cracked gas oil quench and tar bottoms quench injected into the transfer line is sufficient to maintain the temperature in the transfer line at about 525 to 600F., while maintaining a liquid phase on the wall of the transfer line in order to prevent coking and plugging of the transfer line.
  • the quenched effluent is then introduced into a combined quenching and fractionation zone, the gaseous products being 7 cooled by being brought successfully into contact with the cooled distillate fractions either removed or recovered from the quenched tower.
  • the gaseous stream that is recovered from the top of the quenched tower is taken overhead and passed into a settling drum to separate out water, condensed oil, and uncondensed gaseous hydrocarbon products containing principally olefins and diolefins.
  • a sidestream may be withdrawn from the quench tower to remove cycle oil boiling in the intermediate range between the overhead and bottoms products. This may be necessary to control the boiling range of the distillate oil to permit generation of 100 to 150 psig steam.
  • the sidestream is usually steam stripped to recover absorbed light hydrocarbon products.
  • the above-described novel quench system results in recovering about 0.85 X 1800 psig steam by passing the gaseous effluent from the furnace to the initial transfer line heat exchanger. Additional heat is recovered i.e., 0.15 X BTU/hr, in the range of from about 100 to about 150 psig steam in initially cooling the steamcracked gas oil distillate fraction removed from the middles of the quench tower, before recycling as a quench oil to the transfer line. Additionally, a lower upper part of the quench tower for cooling and reflux purposes.
  • hydrocarbon feedstock is a naphtha fraction boiling in the range from about 100 to about 350F.

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Abstract

In quenching the hot gaseous effluent from a naphtha steamcracking operation employing transfer line heat exchangers, improved heat recovery is obtained by recycling a high boiling fraction, i.e., filtered steam-cracked tar bottoms, to the quench point in addition to quenching with a steam-cracked gas oil fraction recovered from the quench tower. The use of the highboiling fraction, i.e., tar bottoms, in conjunction with the steam-cracked gas oil fraction to quench the effluent which has previously passed through a transfer line heat exchanger, maintains the temperature of the effluent passing to the quench tower in the range of from about 500* to about 650*F. while insuring a liquid phase on the walls of the transfer line to prevent fouling, and thus allows additional high-level heat recovery in the quench tower.

Description

[ 1 Dec.2, 1975 1 NAPHTHA STEAM-CRACKING QUENCH PROCESS [75] Inventor: Walter C. Kohfeldt, Madison, NJ.
[73] Assignee: Exxon Research & Engineering Co.,
Linden, NJ.
[22] Filed: May 30, 1973 [21] Appl. No.: 365,052
Related US. Application Data [63] Continuation of Ser. No. 119,485, March 1, 1971,
3,597,494 8/1971 Bigache ct al. 260/683 3,647,907 3/1972 Sato et a1 260/683 3.676.519 7/1972 Dom et a] 260/683 Primary ExaminerDelbert E. Gantz Assistant Examiner-C. E. Spresser Attorney, Agent, or Firm-Donald C. Caulfield [57] ABSTRACT In quenching the hot gaseous effluent from a naphtha steam-cracking operation employing transfer line heat exchangers, improved heat recovery is obtained by recycling a high boiling fraction, i.e., filtered steamcracked tar bottoms, to the quench point in addition to quenching with a steam-cracked gas oil fraction recovered from the quench tower. The use of the high boiling fraction, i.e., tar bottoms, in conjunction with the steam-cracked gas oil fraction to quench the effluent which has previously passed through a transfer line heat exchanger, maintains the temperature of the effluent passing to the quench tower in the range of from about 500 to about 650F. while insuring a liquid phase on the walls of the transfer line to prevent fouling, and thus allows additional high-level heat recovery in the quench tower.
3 Claims, 1 Drawing Figure H MEDOE US. Patent Dec. 2, 1975 w &
W. 6. Ko'hfe/df INVENTOR BY ATTORNEY NAPIrITHA STEAM-CRACKING QUENCH PROCESS This is a continuation of application Ser. No. 1 19,485 filed Mar. 1, 197], now abandoned.
FIELD OF THE INVENTION This invention relates to a method of quenching a hot gaseous effluent of steam-cracked naphtha products being transferred from a cracking coil outlet into a quench tower for separation of the products into fractions. More particularly, this invention relates to an improved steam-cracking quench process wherein the ef fluent from the furnace is first passed through a heat exchanging zone and thereafter quenched with a circulating quench oil fraction, i.e., steam-cracked gas oil recovered as a distillate fraction from the quenching and fractionationzone. i.e., quench tower and with a high boiling fraction such as filtered steam cracker tar bottoms recycled from the quench tower to the quench point Employing such a novel quench system allows the temperature of the effluent passing to the quench tower to be maintained at a temperature in the range of from about 500 to about 650F. while at the same time maintaining a liquid phase on the wall of the transfer line or order to prevent fouling thereof. Accordingly, high-level heat recovery is obtained by first passing the effluent from the furnace through a transfer line heat exchanger and, after employing the quench system heretofore described, passing the effluent at a preferred temperature in the range of from about 525 to about 600F. into the quench tower such that a significant amount of high-level heat is further recovered when the circulating quench oil fraction is removed from the quench tower, passed through one or more heat exchangers and thereafter employed as a quenching medium at the transfer line quench point and in the quench tower itself.
DESCRIPTION OF THE PRIOR ART In steam-cracking virgin naphtha fractions to produce high yields of C to C olefins and diolefins using cracking conditions at high temperatures and low pressures, quick quenching and fast separation of products are necessary. It is necessary to quench the product from the cracking zone; that is, chill, cool them suddenly and rapidly to a lower temperature to prevent or minimize side reactions which reduce yields of desired products and increase yields of undesired products.
In the prior art there are numerous disclosures of different quenching agents or mediums and among these are high-boiling hydrocarbons, low-boiling hydrocarbons, water, steam, and the like. In many cases fouling occurs at or beyond the quench point or region and the process must be terminated to clean the equipment. Simultaneously, when naptha-cracking operation eco nomics favor the use of transfer line heat exchangers to quench the effluent from the steam-cracking furnace, it is important to maximize the level of heat recovered in the quenching process in order to generate high pressure steam for turbine drivers and the like.
In conventional naphtha steam-cracking quench systems, the effluent is quenched with a steam-cracked oil distillate fraction recovered from the quench tower and recycled to the quench point. The use of this fraction as the quench oil lowers the temperature to a range of from about 5 to about'600F., permitting substantial recovery of high-level heat, i.e., recovering X BTU per hour as 125 to about 145 psig steam generation in the quench tower equipment. However, when one or more transfer line heat exchangers are employed to initially cool the effluent from the furnace and to recover a substantial amount of heat, i.e., about 0.85 X BTU/hr. as 1200 to about 1800 psig high-pressure steam, a considerably lower temperature after oil quench must be employed in order to maintain the liquid phase on the walls of the transfer line passing to the quench tower in order to prevent fouling and plugging of the transfer line. This operation lowers the temperature of the effluent in the transfer line to from about 350 to about 425F. such that only a low-level heat recovery is economical in the quench tower, i.e., 0.15 X BTU/hr. as 25 psig steam.
SUMMARY OF THE INVENTION cordance with the instant invention, a high-boiling fraction such as filtered steam-cracked tar bottoms recovered from the quench tower is recycled along with a steam-cracked oil distillate fraction recovered from the quench tower to the quench point in order to maintain the temperature of the effluent in the transfer line in the range of from about 525F. to about 600F. while at the same time maintaining a liquid phase on the wall of the transfer line passing to the quench tower in order to recover 0.85 X BTU/hr. as about 1800 psig steam and 0.15 X BTU(hr. as to about psig steam. Thus, the instant quenching scheme allows the effluent to pass into the quench tower at a sufficient temperature to provide for substantial high-level heat recovery in the quench tower equipment and at the same time provides a liquid phase on the wall of the transfer line passing from the quench point to the quench tower in order to prevent plugging and fouling therein.
The manner of quenching the high temperature steam-cracked naphtha products and obtaining the quick separation of these products into suitable fractions while allowing for an improved heat recovery will be further understood by reference to the accompanying drawing.
Referring to FIG. 1, which shows a diagrammatic flow plan of the naphtha steam-cracking quench system of the instant invention, a hydrocarbon feedstock 1 is passed by line 2 into a preheat and cracking coil located within the cracking furnace 3, wherein the cracking coil is exposed to high intensity radiant heat. The preferred hydrocarbon feedstock is a naphtha fraction containing principally C,-,C saturated aliphatic hydrocarbons, i.e., paraffins or naphthenes, boiling principally in the range from about 100 to 350F. The feedstock may have a somewhat narrower boiling range, e.g., in the range of from about 100 to about F.
A suitable proportion of steam passing by way of line 4 is added to the hydrocarbon feed to make the resulting cracking mixture contain from about 40 to about 65 mole steam, thus substantially lowering the partial pressure of the hydrocarbons. In the cracking coil located within furnace 3, the naphtha hydrocarbons mixed with steam are heated to an outlet temperature in the range of from about l450 to about 1650F., preferably in the range of from about 1500 to loO0F.
The total pressure of the cracked reaction mixture is in the range of from about 1.5 to 3 atmospheres, and preferably less than 30 pounds per square inch absolute. The residence time of the cracked reaction mixture of steam and hydrocarbons in the cracking coil is in the range of from about 0.] to about 0.6 seconds, and more preferably for about 0.3 to about 0.5 seconds. On leav ing the outlet of the coil, the cracked reaction of products is transferred by way of line 5 to transfer line heat exchanger 6. The temperature (cot) of the reaction products leaving the outlet of the coil is in the range of from about l450 to 1650F., and more preferably from about l500 to 1600F. After passing through heat exchanger 6, the effluent is cooled to a temperature below about 850F., and preferably to a temperature in the range of from about 650 to about 8l5F. The heat recovered by the effluent passing through the heat exchanger generates steam in the range of from about 600 to about 1800 psig steam, preferably from about 1400 to 1800 psig.
The effluent having been quenched in the transfer line heat exchanger to a temperature in the range from about 650 to about 815F. is passed by way ofline 7 to the quench tower 8. A steam-cracked oil fraction is withdrawn from the lower portion of the quench tower 8 at a temperature in the range of from about 450 to 550F. through line 9 and is passed by pump 10 through line 1] for cooling in heat exchanger 12. Heat recovered in heat exchanger 12 generates steam in the range of from about 100 to about 150 psig. The cooled oil distillate fraction leaving the heat exchanger 12 at a tern perature in the range of from about 350 to about 400 F. through line 13 becomes divided into two streams. One stream of the cooled oil distillate fraction is passed through line 14 for further cooling in the second heat exchanging zone 15. Heat recovered in heat exchanger 15 generates steam in the range of from about 10 to about 30 psig. The oil distillate cooled in the heat exchanger 15 is passed by line 16 into the top section of the quench tower for partial cooling of the vapors flowing upwardly through quench tower 8. A sufficient amount of the oil distillate having a temperature in the range of from about 350 to about 400F. is passed from line 13 into line 14 and is injected at one or more points into line 7 to effect the lowering of the temperature in the effluent passing from the transfer line heat exchanger to a temperature in the range of from about 525 to about 600F. The steam-cracked oil distillate fraction which is injected into line 7 by way of line 14 has a preferred boiling range of from about 350 to about 750F., and more preferably from about 450 to about 650F. The flow rate of the oil distillate from line 14 into line 7 is in the range of from about 0.3 to about 0.8 parts by weight of the oil fraction per one part by weight of the effluent from the furnace, the oil fraction having a temperature in the range of from about 350 to about 400F.
The bottoms fraction is withdrawn from quench tower 8 at a temperature in the range of from about 525 to about 600F. through line 17 and is passed by pump 18 through line 19 to a filter 20. The bottoms product recovered from quench tower 8 to line 7 comprises steam-cracked tar bottoms. The coke and other carbonaceous particles present in said product are removed in the filter 20 and tower bottoms pass by way of line 21 for cooling in heat exchanger 22. A sufficient amount of the cooled high-boiling fraction is recovered from heat exchanger 22 and passed by way of line 23 through line 24- and injected into line 7 at one or more points in order to maintain a liquid phase on the wall of line 7. The boiling point'of the material. i.e.. steamcracked tar bottoms passing by way of line 24 is in the range of from about 550 to about 800F. The flow rate from line 24 into line 7 is in the range of from about 0.01 to about 0.03 parts by weight of the bottoms product passing by way of line 24 per one part by weight of the sum of the effluent and oil distillate, the temperature of the high-boiling material passing by way of line 24 being in the range of about 130 to about 250F.
The mixture of the cracked products and the steamcracked oil fraction and high-boiling bottoms fraction passing by way of line 7 is preferably introduced into the bottom of the quench tower at a temperature in the range from about 525 to 600F.
gaseous vapors containing steam-cracked hydrocarbon products boiling below about 450F., steam, and hydrogen is taken overhead from the tower 8 through line 25. This gaseous stream is passed by way of line 25 into condenser 26 which is operated at a sufficiently low temperature to condense out water and hydrocarbons having more than about 7 carbon atoms per molecule. The condensate is then passed by way of line 27 into a separation tank 28 wherein the liquid condensate is settled so that a lower water layer can be withdrawn to line 29 and condensed oil can be withdrawn from an upper liquid layer through line 30. Uncondensed gaseous hydrocarbon products containing principally oletins and diolefins having up to about 6 carbon atoms per molecule are withdrawn from vessel 28 to line 33 to be subjected to light ends processing i.e., recover ethylene, propylene, butenes, butadienes and the like. A portion of the condensed oil withdrawn from settling drum 28 by way of line 30 is passed by way of line 31 into the upper portion of quench tower 8 to form a reflux medium for the top of the tower.
The interior of quench tower 8 is equipped with plates 32 for obtaining contact between the liquid and vapor but allowing for the fast flow of materials. The necessary cooling is obtained in the upper part of the quench tower 8 by the injection of the cooled oil distillate fraction introduced to the tower by way of line 16 and by introducing the condensed oil introduced by way of line 31. Each of these streams is introduced in suitable amounts and at the proper temperatures at several space points in order to obtain the optimum cooling and fractionation. The temperature of the vapors at EXAMPLE While various virgin naphtha fractions may be employed as the feedstocks of the instant invention, a preferred feed contains hydrocarbons boiling principally in the range of to 300F. The feed is cracked at temperatures of about 1500F. in the presence of a sufficient amount of steam to make the hydrocarbon partial pressure about 14 lbs. per square inch absolute. The cracked products leave the outlet coil at about 1500F. and are then introduced into the transfer line heat exchanger. The cracked products are recovered from the transfer line heat exchanger at a temperature in the range of from about 650F. to 8l5F. The effluent is then quenched by a steam-cracked gas oil distillate fraction being removed from the lower section of the quench tower, and after passing through a heat exchanger is injected into the quench point or points at a temperature of about 375F., the proportion of steamcracked oil quench being about 0.5 times the weight of the admixed hydrocarbon products which are being quenched. Simultaneously, a steam-cracked tar bottoms fraction having a boiling point of about 750F. is removed from the bottom of the quench tower, and after being filtered and passed through a heat exchanger such that the temperature of the tar fraction is about 200F., is injected at said temperature into the quench points in the transfer line, the proportion of tar bottoms quench oil being 0.02 times the weight of the admixed cracked hydrocarbon products and steamcracked oil quench which are passing in the transfer line to the quench tower.
The amount of steam-cracked gas oil quench and tar bottoms quench injected into the transfer line is sufficient to maintain the temperature in the transfer line at about 525 to 600F., while maintaining a liquid phase on the wall of the transfer line in order to prevent coking and plugging of the transfer line. The quenched effluent is then introduced into a combined quenching and fractionation zone, the gaseous products being 7 cooled by being brought successfully into contact with the cooled distillate fractions either removed or recovered from the quenched tower. The gaseous stream that is recovered from the top of the quenched tower is taken overhead and passed into a settling drum to separate out water, condensed oil, and uncondensed gaseous hydrocarbon products containing principally olefins and diolefins.
A sidestream may be withdrawn from the quench tower to remove cycle oil boiling in the intermediate range between the overhead and bottoms products. This may be necessary to control the boiling range of the distillate oil to permit generation of 100 to 150 psig steam. The sidestream is usually steam stripped to recover absorbed light hydrocarbon products.
The above-described novel quench system results in recovering about 0.85 X 1800 psig steam by passing the gaseous effluent from the furnace to the initial transfer line heat exchanger. Additional heat is recovered i.e., 0.15 X BTU/hr, in the range of from about 100 to about 150 psig steam in initially cooling the steamcracked gas oil distillate fraction removed from the middles of the quench tower, before recycling as a quench oil to the transfer line. Additionally, a lower upper part of the quench tower for cooling and reflux purposes.
What is claimed is:
1. In a process of treating a hydrocarbon feed stock in a steam-cracking furnace at elevated temperatures and low hydrocarbon partial pressures to form unsaturated hydrocarbon products wherein a quenching medium is introduced into the effluent from the furnace and thereater passing said effluent through a transfer line heat exchanger to the quench tower, the improvement which comprises passing said effluent from the furnace through a transfer line heat exchanger zone to lower the temperature of said products below about 850F. and thereafter contacting said products passing to the quenching and fractionation zone with:
a. from about 0.3 to about 0.8 parts by weight of a steam-cracked oil fraction recovered from the quench tower per one part by weight of the effluent from the furnace, said steam-cracked oil fraction having been withdrawn from the quench tower at a temperature in the range of from about 450 to about 550F. and therafter passed through a heat exchanging zone in order to recover high level heat in an amount in order to generate steam in the range of from about to about psig; and
b. from about 0.01 to about 0.03 parts by weight of a bottom fraction recovered from said quenching tower per one part by weight of the sum of the effluent and the steam-cracked oil fraction, said fraction boiling in the range of from about 500 to about 800F. to lower the temperature of the products passing through the transfer line to the quench tower to a range of from about 525 to about 600F. in order to maintain a liquid phase on the wall of said transfer line.
2. The process as described in claim 1 wherein the hydrocarbon feedstock is a naphtha fraction boiling in the range from about 100 to about 350F.
3. The process of claim 1 wherein a portion of the steam-cracked gas oil fraction which has been cooled to a temperature in the range of from about 350 to about 400F. is passed through a second heat exchanging zone in order to further generate steam in the range of from about 10 to about 30 psig. l

Claims (3)

1. A PROCESS OF TREATING A HYDROCARBON FEED STOCK IN A STEAM-CRACKING FURNACE AT ELEVATED TEMPERATURES AND LOW HYDROCARBON PARTIAL PRESSURES TO FORM UNSATURATED HYDROCARBON PRODUCTS WHEREIN A QUENCHING MEDIUM IS INTRODUCED INTO THE EFFLUENT FROM THE FURNACE AND THEREAFTER PASSING SAID EFFLUENT THROUGH A TRANSFER LINE HEAT EXCHANGER TO THE QUENCH TOWER, THE IMPROVEMENT WHICH COMPRISES PASSING SAID EFFLUENT FROM THE FURNACE THROUGH A TRANSFER LINE HEAT EXCHANGER ZONE TO LOWER THE TEMPERATURE OF SAID PRODUCTS BELOW ABOUT 850*F. AND THEREAFTER CONTACTING SAID PRODUCTS PASSING TO THE QUENCHING AND FRACTIONATION ZONE WITH: A. FROM ABOUT 0.3 TO ABOUT 0.8 PARTS BY WEIGHT OF A STEAMCRACKED OIL FRACTION RECOVERED FROM THE QUENCH TOWER PERONE PART BY WEIGHT OF THE EFFLUENT FROM THE FURNACE, SAID STEAM-CRACKED OIL FRACTION HAVING BEEN WITHDRAWN FROM THE QUENCH TOWER AT A TEMPERATURE IN THE RANGE OF FROM ABOUT 450* TO ABOUT 550*F. AND THEREAFTER PASSED THROUGH A HEAT EXCHANGING ZONE IN ORDER TO RECOVER HIGH LEVEL HEAT
2. The process as described in claim 1 wherein the hydrocarbon feedstock is a naphtha fraction boiling in the range from about 100* to about 350*F.
3. The process of claim 1 wherein a portion of the steam-cracked gas oil fraction which has been cooled to a temperature in the range of from about 350* to about 400*F. is passed through a second heat exchanging zone in order to further generate steam in the range of from about 10 to about 30 psig.
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Cited By (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4212726A (en) * 1977-11-23 1980-07-15 Cosden Technology, Inc. Method for increasing the purity of hydrogen recycle gas
FR2463177A1 (en) * 1979-08-07 1981-02-20 Uop Inc Visbreaking with improved quenching before passing to flash zone - using liq. mixt. having relatively low viscosity
US4404087A (en) * 1982-02-12 1983-09-13 Phillips Petroleum Company Antifoulants for thermal cracking processes
US4446003A (en) * 1981-06-02 1984-05-01 British Gas Corporation Heat recovery process and apparatus
EP0911378A2 (en) * 1997-10-27 1999-04-28 The M. W. Kellogg Company Quench oil viscosity control in pyrolysis fractionator
US20040267076A1 (en) * 2001-11-06 2004-12-30 Font Freide Josephus Johannes Helena Maria Olefins production process
US20050008796A1 (en) * 2001-11-09 2005-01-13 Uwe Kriltz Fire-resisting glass
WO2006063201A1 (en) * 2004-12-10 2006-06-15 Bhirud Vasant L Steam cracking with naphtha dearomatization
US20070007170A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007175A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007173A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007169A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007172A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007171A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20070007174A1 (en) * 2005-07-08 2007-01-11 Strack Robert D Method for processing hydrocarbon pyrolysis effluent
US20080099371A1 (en) * 2006-10-30 2008-05-01 Mccoy James N Process for upgrading tar
EP2082010A2 (en) * 2006-09-28 2009-07-29 Uop Llc Process for enhanced olefin production
US20090194458A1 (en) * 2008-01-31 2009-08-06 Ou John D Y Process and Apparatus for Upgrading Steam Cracked Tar
US20090255852A1 (en) * 2008-04-09 2009-10-15 Ou John D Y Process and Apparatus for Upgrading Steam Cracked Tar Using Steam
US20110308995A1 (en) * 2010-06-16 2011-12-22 Marathon Oil Canada Corporation Dual reactor for better conversion of heavy hydrocarbons
WO2012015494A2 (en) 2010-07-30 2012-02-02 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
US8118996B2 (en) 2007-03-09 2012-02-21 Exxonmobil Chemical Patents Inc. Apparatus and process for cracking hydrocarbonaceous feed utilizing a pre-quenching oil containing crackable components
WO2012158450A3 (en) * 2011-05-13 2013-04-11 Catalytic Distillation Technologies Method for producing high vcm coke
WO2013149721A1 (en) * 2012-04-05 2013-10-10 Linde Aktiengesellschaft Method for separating olefins with gentle cleavage
US8663458B2 (en) 2011-02-03 2014-03-04 Chemical Process and Production, Inc Process to hydrodesulfurize pyrolysis gasoline
US9534174B2 (en) 2012-07-27 2017-01-03 Anellotech, Inc. Fast catalytic pyrolysis with recycle of side products
US9790179B2 (en) 2014-07-01 2017-10-17 Anellotech, Inc. Processes for recovering valuable components from a catalytic fast pyrolysis process
WO2021016306A1 (en) * 2019-07-24 2021-01-28 Exxonmobil Chemical Patents Inc. Processes and systems for fractionating a pyrolysis effluent
US11124708B2 (en) * 2014-10-13 2021-09-21 Total Research & Technology Feluy Process for the production of high value chemicals from biologically produced materials

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2340778A (en) * 1940-06-21 1944-02-01 Clinton C Steward Process for producing olefins and motor fuel
US2366521A (en) * 1943-02-25 1945-01-02 Standard Oil Dev Co Method of removing coke deposits from high-temperature oil lines
US2943041A (en) * 1958-06-09 1960-06-28 Exxon Research Engineering Co Processing of steam-cracked naphtha light end products
US3180904A (en) * 1959-05-15 1965-04-27 Hoechst Ag Process for the manufacture of olefins
US3580838A (en) * 1969-02-24 1971-05-25 Lummus Co Hydrocarbon pyrolysis process
US3597494A (en) * 1968-09-04 1971-08-03 Inst Francais Du Petrole Steam-cracking of hydrocarbons
US3647907A (en) * 1968-09-06 1972-03-07 Mitsubishi Petrochemical Co Process for quenching a gas obtained by thermal cracking of hydrocarbons
US3676519A (en) * 1970-01-02 1972-07-11 Lummus Co Quench process

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2340778A (en) * 1940-06-21 1944-02-01 Clinton C Steward Process for producing olefins and motor fuel
US2366521A (en) * 1943-02-25 1945-01-02 Standard Oil Dev Co Method of removing coke deposits from high-temperature oil lines
US2943041A (en) * 1958-06-09 1960-06-28 Exxon Research Engineering Co Processing of steam-cracked naphtha light end products
US3180904A (en) * 1959-05-15 1965-04-27 Hoechst Ag Process for the manufacture of olefins
US3597494A (en) * 1968-09-04 1971-08-03 Inst Francais Du Petrole Steam-cracking of hydrocarbons
US3647907A (en) * 1968-09-06 1972-03-07 Mitsubishi Petrochemical Co Process for quenching a gas obtained by thermal cracking of hydrocarbons
US3580838A (en) * 1969-02-24 1971-05-25 Lummus Co Hydrocarbon pyrolysis process
US3676519A (en) * 1970-01-02 1972-07-11 Lummus Co Quench process

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4212726A (en) * 1977-11-23 1980-07-15 Cosden Technology, Inc. Method for increasing the purity of hydrogen recycle gas
FR2463177A1 (en) * 1979-08-07 1981-02-20 Uop Inc Visbreaking with improved quenching before passing to flash zone - using liq. mixt. having relatively low viscosity
US4446003A (en) * 1981-06-02 1984-05-01 British Gas Corporation Heat recovery process and apparatus
US4404087A (en) * 1982-02-12 1983-09-13 Phillips Petroleum Company Antifoulants for thermal cracking processes
EP0911378A2 (en) * 1997-10-27 1999-04-28 The M. W. Kellogg Company Quench oil viscosity control in pyrolysis fractionator
EP0911378A3 (en) * 1997-10-27 1999-10-27 Kellogg Brown & Root, Inc. Quench oil viscosity control in pyrolysis fractionator
KR100587761B1 (en) * 1997-10-27 2006-08-30 더 엠. 더블유. 켈로그 컴파니 Quench oil viscosity control in pyrolysis fractionator
US20040267076A1 (en) * 2001-11-06 2004-12-30 Font Freide Josephus Johannes Helena Maria Olefins production process
US7763763B2 (en) * 2001-11-06 2010-07-27 Bp Exploration Operating Company Limited Olefins production process
US20050008796A1 (en) * 2001-11-09 2005-01-13 Uwe Kriltz Fire-resisting glass
US20080194900A1 (en) * 2004-12-10 2008-08-14 Bhirud Vasant L Steam Cracking with Naphtha Dearomatization
WO2006063201A1 (en) * 2004-12-10 2006-06-15 Bhirud Vasant L Steam cracking with naphtha dearomatization
US7749372B2 (en) 2005-07-08 2010-07-06 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
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WO2007008397A1 (en) 2005-07-08 2007-01-18 Exxonmobil Chemical Patents Inc. Method for processing hydrocarbon pyrolysis effluent
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