Classifications

• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING 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
  • C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
  • C10G9/14—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils in pipes or coils with or without auxiliary means, e.g. digesters, soaking drums, expansion means
  • C10G9/18—Apparatus
  • C10G9/20—Tube furnaces

Definitions

• the present invention relates to the cracking of hydrocarbon feedstocks, particularly those that contain relatively non-volatile hydrocarbons and other contaminants.
• the present invention relates to cooling hot liquid bottoms taken from a vapor- liquid separation apparatus used in steam cracking hydrocarbon feedstocks, while preheating a hydrocarbon feedstock to a pyrolysis furnace.
• Steam cracking also referred to as pyrolysis
• pyrolysis has long been used to crack various hydrocarbon feedstocks into olefins, preferably light olefins such as ethylene, propylene, and butenes.
• Conventional steam cracking utilizes a pyrolysis furnace which has two main sections: a convection section and a radiant section.
• the hydrocarbon feedstock typically enters the convection section of the furnace as a liquid (except for light feedstocks which enter as a vapor) wherein it is typically heated and vaporized by indirect contact with hot flue gas from the radiant section and by direct contact with steam.
• the vaporized feedstock and steam mixture is then introduced into the radiant section where the cracking takes place.
• the resulting products, including olefins leave the pyrolysis furnace for further downstream processing, including quenching.
• non-volatiles Only very low levels of non-volatiles, say, e.g., less than 50 ppmw, or even less than 5 ppmw can be tolerated in the convection section downstream of the point where the lighter components have fully vaporized. Additionally, some naphthas are contaminated with crude oil during transport. Conventional pyrolysis furnaces do not have the flexibility to process resids, e.g., atmospheric resids, crudes, or many resid- or crude-contaminated gas oils or naphthas, which contain a large fraction of heavy non- volatile hydrocarbons, say, from 50 to 100000 ppmw.
• resids e.g., atmospheric resids, crudes, or many resid- or crude-contaminated gas oils or naphthas, which contain a large fraction of heavy non- volatile hydrocarbons, say, from 50 to 100000 ppmw.
• the crude oil or resid is typically preheated and mixed with dilution steam, and only partially vaporized before it is removed from the convection section and fed to a vapor-liquid separator (flash drum or flash vessel) to separate heavy non-volatile hydrocarbons from lighter volatile hydrocarbons which are fed back to the convection section of the furnace for additional preheating and then cracked in the radiant section of the pyrolysis furnace. It is important to maximize non-volatile hydrocarbon removal efficiency in this process. Otherwise, heavy, coke-forming non-volatile hydrocarbons could be entrained in the vapor phase and carried overhead into the furnace creating coking problems in the convection section.
• U.S. Patent 3,617,493 which is incorporated herein by reference, discloses the use of an external vaporization drum for the crude oil feed and discloses the use of a first flash to remove naphtha as vapor and a second flash to remove vapors with a boiling point between 230° C and 590° C (450° F and 1100° F). The vapors are cracked in the pyrolysis furnace into olefins and the separated liquids from the two flash tanks are removed, stripped with steam, and used as fuel.
• U.S. Patent 3,617,493 which is incorporated herein by reference, discloses the use of an external vaporization drum for the crude oil feed and discloses the use of a first flash to remove naphtha as vapor and a second flash to remove vapors with a boiling point between 230° C and 590° C (450° F and 1100° F). The vapors are cracked in the pyrolysis furnace into olefins and the separated liquids from the two flash tanks
• Patents 7,097,758 and 7,138,047 both of which are incorporated by reference herein, disclose furnaces for processing high levels of non- volatile hydrocarbons (or resids) wherein the feedstocks are preheated, mixed with dilution steam and water, partially vaporized in the convection section and then fed to a vapor-liquid separator to remove non-volatiles as liquid, prior to cracking.
• a vapor-liquid separator to remove non-volatiles as liquid, prior to cracking.
• Patent 7,138,047 describes an advantageously controlled process to optimize the cracking of volatile hydrocarbons contained in the heavy hydrocarbon feedstocks and to reduce and avoid coking problems. It provides a method to maintain a relatively constant ratio of vapor to liquid leaving the flash by maintaining a relatively constant temperature of the stream entering the flash. More specifically, the constant temperature of the flash stream is maintained by automatically adjusting the amount of a fluid stream mixed with the heavy hydrocarbon feedstock prior to the flash.
• a variable quantity of a dilution liquid (or fluid), preferably water, is substituted for dilution steam as required to keep the vapor-liquid separator (flash) temperature substantially constant, despite load changes that the furnace may experience.
• the bottoms from the flash can be cooled in a heat exchanger and exported or recycled to the flash drum.
• At least the first stage of cooling can be achieved in a heat exchanger located in close proximity to the vapor-liquid separator. This heat exchanger has been used in the past to cool the liquid stream from the separator by generating medium pressure steam (693 to 1138 kPa (100 to 150 psig)) which can be exported to the plant medium pressure steam header.
• medium pressure steam (693 to 1138 kPa (100 to 150 psig)
• U.S. Patent 7,351,872 incorporated herein by reference, teaches alternate ways of maintaining vapor-liquid separator temperature, e.g., by varying furnace draft, which can dispense with the need for water injection entirely.
• U.S. Patent Application Ser. No. 12/132,130, filed June 3, 2008 discloses cooling liquid bottoms taken from a vapor-liquid separation apparatus used in steam cracking hydrocarbon feeds, by heat exchange with high pressure boiler feed water.
• the present invention relates to a process for cooling liquid bottoms from a vapor-liquid separator used in separating heated hydrocarbon feedstock that is to be cracked, which comprises: i) indirectly heat exchanging hot liquid bottoms, e.g., having a temperature ranging from 200° C to 500° C (392° F to 932° F), say, from 250° C to 350° C (482° F to 662° F), with a cool hydrocarbon feedstock, e.g., having a temperature ranging from 20° C to 200° C (68° F to 392° F), say, from 50° C to 150° C (122° F to 302° F), to provide cooled liquid bottoms, e.g., at a temperature ranging from 50° C to 350° C (122° F to 662° F), say, from 70° C to 300° C (158° F to 572° F), and preheated hydrocarbon feedstock, e.g., at a
• Step ii)'s directing of the preheated hydrocarbon feedstock to the convection section inlet results in additional heating and subsequent cracking of the feedstock.
• the cool hydrocarbon feedstock can typically contain "resid,” described further below.
• hot liquid bottoms can be defined as a liquid bottoms stream of sufficient heat content for transfer to a cooler stream using an indirect heat exchanger.
• cool hydrocarbon feedstock can be defined as a hydrocarbon feedstock stream which is sufficiently cool to accept heat transferred from a hotter stream using an indirect heat exchanger.
• the temperature difference between the hot liquid bottoms and the cool hydrocarbon feedstock can be at least 25° C (77° F), say, at least 100° C (212° F), e.g., at least 200° C (392° F).
• the process of the invention further comprises: iii) introducing diluent steam to the preheated hydrocarbon feedstock; and, optionally, iv) introducing a liquid diluent to the preheated hydrocarbon feedstock.
• the introduced liquid diluent typically comprising water, can be reduced as a function of the extent to which the hydrocarbon feedstock is preheated.
• the introduced liquid diluent can be substituted for the steam diluent in an amount sufficient to maintain a substantially constant temperature in the vapor- liquid separator.
• the hydrocarbon feedstock can vary from heavier feedstocks selected from heavy crude oil and atmospheric resid, to lighter feedstocks selected from lighter crude oils and mixtures of crude oil and condensate.
• the present invention relates to a process for cracking a hydrocarbon feedstock in a pyrolysis furnace comprising at least one convection section and a radiant section, the process comprising: (a) introducing a preheated hydrocarbon feedstock, for further heating in a convection zone, such as but not limited to an upper convection zone; (b) mixing the preheated hydrocarbon feedstock with dilution steam and, optionally, a dilution liquid, e.g., water, to form a mixture stream; (c) separating the mixture stream in a vapor-liquid separator to form I) a vapor phase and II) a liquid phase; (d) removing the vapor phase as overhead and the liquid phase as bottoms from the vapor-liquid separator; (e) cooling the hotter bottoms in a heat exchanger outside the pyrolysis furnace by indirect heat exchange with a cooler hydrocarbon feedstock to provide at least a portion of the preheated hydrocarbon feedstock; (f) crack
• the mixture stream is heated in an additional convection zone prior to its introduction to the vapor-liquid separator.
• the vapor phase is heated in an additional convection zone prior to cracking.
• the at least one convection zone comprises a tube bank heat exchanger.
• the process further comprises quenching the effluent comprising olefins from cracking, prior to recovering cracked product.
• the process further comprises recycling a portion of the cooled liquid bottoms to the vapor- liquid separator.
• the process can further comprise at least one of: (h) heat exchanging high pressure boiler feed water with hot flue gas in a convection zone to provide preheated high pressure boiler feed water; (i) heat exchanging dilution steam with hot flue gas in a convection zone to provide heated dilution steam; (j) optionally adding desuperheater water to the heated dilution steam, providing a cooled mixture; (k) adding the heated dilution steam and optional desuperheater water to the mixture stream of (b); (1) heat exchanging superheated high pressure steam with hot flue gas in a convection zone to provide heated superheated high pressure steam; (m) adding desuperheater water to the heated superheated high pressure steam to provide a stream of superheated high pressure steam at reduced temperature; and (n)
• Such temperature can be at least 370° C (700° F), typically ranging from 477° C to 565° C (890° F to 1050° F).
• temperatures for a specific stream to be heated or cooled can be measured at the appropriate inlet or outlet of the heat exchange means from which they are received or taken, unless otherwise described.
• the liquid bottoms from the vapor-liquid separation apparatus range from 250° C to 350° C (482° F to 662° F)
• the cooled liquid bottoms range from 90° C to 260° C (194° F to 500° F)
• the hydrocarbon feedstock ranges from 70° C to 150° C (158° F to 302° F)
• the preheated hydrocarbon feedstock ranges from 90° C to 200° C (194° F to 392° F).
• the dilution liquid used to form the mixture stream of (b) is reduced as a function of the extent to which the hydrocarbon feedstock is preheated.
• the dilution liquid is substituted for the dilution steam in an amount sufficient to maintain a substantially constant temperature in the vapor-liquid separator.
• the hydrocarbon feedstock is selected or varied over a range of hydrocarbon liquid feeds, from heavier feedstocks to lighter feedstocks.
• the heavier feedstocks comprise higher boiling fractions than lighter feedstocks.
• Heavier feedstocks can be selected, for example, from heavy crude oil and atmospheric resid, while lighter feedstocks can be selected, for example, from lighter crude oils and mixtures of crude oil and condensate.
• the present invention relates to an apparatus for cracking a preheated hydrocarbon feedstock in a pyrolysis furnace comprising a) a convection section having at least one convection zone, and b) a radiant section, the apparatus comprising: (1) an inlet for receiving preheated hydrocarbon feedstock; (2) a convection zone for heating the preheated hydrocarbon feedstock; (3) at least one inlet for introducing steam, or steam and water, to the heated hydrocarbon feedstock to form a mixture stream; (4) a vapor-liquid separator, which can be external to the pyrolysis furnace, for treating the mixture stream to form I) a vapor phase and II) a liquid phase, the separator further comprising an overhead outlet for substantially removing the vapor phase as overhead and a liquid outlet for substantially removing the liquid phase as heated bottoms from the vapor-liquid separator; (5) a heat exchanger, external to the pyrolysis furnace, for cooling the vapor-liquid separator bottoms by indirect heat exchange,
• the apparatus can further comprise at least one of: (8) a convection zone for heating the mixture stream; (9) a convection zone for heating the overhead to provide a heated vapor phase; (10) a quench exchanger for cooling the effluent comprising olefins; and (11) a recovery train for recovering light olefins from the effluent comprising olefins.
• the at least one convection zone comprises at least one heat exchanger tube bank.
• the apparatus further comprises at least one of: (12) a heat exchanger for preheating high pressure boiler feed water with hot flue gas in a convection zone to provide preheated high pressure boiler feed water; (13) a heat exchanger for heating dilution steam with hot flue gas in a convection zone to provide heated dilution steam; (14) an inlet for adding desuperheater water to the heated dilution steam; (15) an inlet for adding the heated dilution steam to the mixture stream of (3); (16) an inlet for adding desuperheater water to the mixture stream of (3); (17) a heat exchanger for superheating high pressure steam with hot flue gas in a convection zone to provide heated superheated high pressure steam; (18) an inlet for adding desuperheater water to the heated superheated high pressure steam to provide a stream of superheated high pressure steam at reduced temperature; and (19) a heat exchanger for heating the mixture of heated superheated high pressure
• FIGURE illustrates a schematic flow diagram of the overall process and apparatus in accordance with the present invention.
• the present invention provides an efficient way of treating the liquid bottoms from a vapor-liquid separation apparatus, which are associated with a hydrocarbon pyrolysis reactor used for steam cracking.
• the invention provides efficient removal and recovery of heat from the bottoms stream by preheating a hydrocarbonaceous feed to the reactor.
• the hydrocarbon pyrolysis reactor (or furnace) used in the present invention comprises a convection section having at least one convection zone, and a radiant section.
• a convection section can be described as that portion of the furnace wherein a feedstock is treated by convection heating, e.g., by indirect heat exchange of hot flue gas from the radiant section, in passages having heat conducting surfaces, e.g., a bank of metal tubes.
• the convection section typically comprises one or more convection zones, each zone having an inlet to and an outlet from the convection section.
• a convection section can typically comprise one or more heating zones, as well as a preheating zone, although the latter can be redundant in the present invention which preheats feedstock in a heat exchanger utilizing heated bottoms from a vapor-liquid separator.
• Each convection zone is typically associated with a specific tube bank for effecting heat exchange.
• an internal or external vapor- liquid separator e.g., flash drum or vessel, can be interposed between convection zones.
• the convection section may also include separate convection zones which treat other streams, e.g., boiler feed water, steam, etc.
• conditions e.g., temperatures, of a reactant stream or starting material stream are measured at the inlet of the zone in which they are treated, while conditions for a treated stream are typically measured at the outlet of the zone in which they are treated.
• the heat exchanger used to cool the hot liquid bottoms can be any suitable heat exchanger means, e.g., a shell-and-tube exchanger, spiral wound exchanger, airf ⁇ n, or double-pipe exchanger.
• the present invention is used in the steam cracking of hydrocarbon feedstocks, especially liquid hydrocarbon feedstocks, e.g., those having a nominal final boiling point of at least 315° C (600° F). These feedstocks typically contain non-volatile components.
• non-volatile components are the fraction of the hydrocarbon feed with a nominal boiling point above 590° C (1100° F) as measured by ASTM D-6352-98 or D-2887.
• This invention works very well with non-volatiles having a nominal boiling point above 760° C (1400° F).
• the boiling point distribution of the hydrocarbon feed is measured by Gas Chromatograph Distillation (GCD), also measured by ASTM D-6352-98 or D-2887.
• GCD Gas Chromatograph Distillation
• Non-volatiles include coke precursors, which are large, condensable molecules that condense in the vapor, and then form coke under the operating conditions encountered in the present process of the invention.
• Typical hydrocarbon feedstocks suited to use for steam cracking in the present invention are commonly selected from the exemplary group including steam cracked gas oil/residue admixtures, gas oils, heating oil, jet fuel, diesel, kerosene, gasoline, coker naphtha, steam cracked naphtha, catalytically cracked naphtha, hydrocrackate, reformate, raffmate reformate, Fischer-Tropsch liquids, Fischer-Tropsch gases, natural gasoline, distillate, virgin naphtha, crude oil, atmospheric pipestill bottoms, vacuum pipestill streams including bottoms, wide boiling range naphtha to gas oil condensates, heavy non-virgin hydrocarbon streams from refineries, vacuum gas oils, heavy gas oil, naphtha contaminated with crude, atmospheric residue, heavy residue, hydrocarbon gas/residue admixtures, hydrogen/residue admixtures, C4 T s/residue admixtures, naphtha/residue admix
• vapor- liquid separator For heavy crude oils or atmospheric resids, it is usually desired to operate the vapor- liquid separator at the highest possible temperature in order to maximize the quantity of the feed that is recovered to the radiant section of the pyrolysis furnace for cracking to light olefins.
• target temperatures generally fall between 400° C and 500° C (752° F and 932° F).
• the upper limit is typically set by the onset of thermal cracking and fouling in the overhead lines from the vapor-liquid separator, e.g., temperatures of 460° C (860° F).
• the concentration of non-volatile hydrocarbons in the separator bottoms liquid may reach a maximum value prior to the separator temperature reaching the aforesaid upper limit. In such instances, it is desirable to operate the separator at a lower temperature to maintain an adequate quantity and quality of the separator bottoms liquid.
• Such temperatures depend on the boiling range of the feed mixture, and can range from 400° C to 450° C (752° F to 842°
• the liquid bottoms stream from the vapor-liquid separator is cooled prior to being sent to storage or alternative downstream disposition. At least the first stage of cooling can be achieved in a heat exchanger in proximity to the vapor-liquid separator.
• the pyrolysis furnace of U.S. Patent 7,138,047 suitable for use in the present invention, utilizes a mixture of steam and fluid, e.g., water, as diluent, and can be operated in a commercially stable operation on a wide variety of feedstocks containing non-volatile hydrocarbons. However, its operation is most efficient when process feedstocks require a high vapor-liquid separator temperature. In such cases, the rate of water injection into the convection section can be minimized.
• Additional control techniques for a pyrolysis furnace described in U.S. Patent 7,351,872, incorporated herein by reference in its entirety include adjusting furnace draft to control the inlet temperature of the vapor-liquid separator, and can eliminate the need for water injection where feed quality remains consistent.
• the furnace must process not only feedstocks requiring a high separator temperature, e.g., whole crude or atmospheric resid, but feedstocks requiring low separator temperature, e.g., crude oil/condensate mixture, significant quantities of water must be substituted for dilution steam to maintain the separator at the required lower temperature.
• each mass of water injected into the convection section of a furnace in place of dilution steam requires an incremental mass of sour condensate blowdown from the dilution steam generation system. This increases both the cost of the waste water treatment facilities required by the plant in question, and also increases the volume of the treated water discharge from the plant.
• the present invention provides for using a broad range of feedstocks containing non-volatile hydrocarbons to be processed across a reasonable range of vapor- liquid separator temperatures, without requiring injection of significant volumes of water in place of dilution steam in the convection section of the furnace.
• the reduced preheat duty required by lighter feedstocks is balanced by the heat exchange with the low liquid flow rates from the separator bottoms that are associated with lighter feedstocks. This permits efficient and substantially self-regulating energy recovery from the flue gas with minimal water injection into the convection section for both the heavy feedstocks and the light feedstocks.
• the balancing of convection section duties and separator temperatures may also be aided by varying the temperature at which the feed is supplied to the preheat exchanger. For applications requiring high preheat duties, e.g., heavy crude oils, higher supply temperatures are favored. For low preheat duties, e.g., crude oil/condensate mixtures, low supply temperatures are favored. This balancing can further be aided by varying the excess O 2 levels at which the furnace is operated. For applications requiring high preheat duties, higher excess O 2 levels are desirable, for lower preheat duties, lower excess O 2 levels are preferred.
• the hydrocarbon feedstock which typically contains resid, is preheated outside the pyrolysis furnace comprising a convection section with one or more convection zones, and a radiant section, prior to introduction of the hydrocarbon feedstock to the convection zone for initially heating feedstock within the convection section of the pyrolysis furnace.
• the preheating can be carried out by heat exchanging the hydrocarbon feedstock with a suitable source of heat.
• the present invention utilizes as the heat source a hot liquid bottoms stream taken from a vapor-liquid separator that is located downstream of the initial convection zone for heating feedstock in the convection section of the pyrolysis furnace, and upstream of the radiant section of the pyrolysis furnace.
• the preheated hydrocarbon feedstock can be further heated by indirect contact with flue gas in a convection zone tube bank of the pyrolysis furnace before mixing with a fluid, e.g., steam, and optionally, liquid water.
• a fluid e.g., steam, and optionally, liquid water.
• the temperature of the hydrocarbon feedstock is from 130° C to 260° C (266° F to 500° F), before mixing with the fluid.
• the mixture stream may be heated by indirect contact with flue gas in the convection section of the pyrolysis furnace before being flashed.
• the convection section is arranged to add the primary dilution steam stream and any liquid water, between convection zones such that the hydrocarbon feedstock can be heated before mixing with the fluid and the mixture stream can be further heated before being flashed.
• the temperature of the flue gas entering the uppermost (or furthest upstream) convection zone tube bank for heating feedstock is generally less than 815° C (1500° F), for example, less than 705° C (1300° F), such as less than 620° C (1150° F), and preferably less than 540° C (1000° F).
• Dilution steam may be added at any point in the process, for example, it may be added to the hydrocarbon feedstock before or after heating, to the mixture stream, and/or to the vapor phase.
• Any dilution steam stream may comprise sour steam.
• Any dilution steam stream may be heated or superheated in a convection zone tube bank located anywhere within the convection section of the furnace.
• the mixture stream may be at 315° C to 540° C (600° F to 1000° F) before introduction to the vapor- liquid separator or flash apparatus, e.g., knockout drum, and the flash pressure may be 275 to 1375 kPa (40 to 200 psia). Following the flash, 50 to 98% of the mixture stream may be in the vapor phase.
• An additional separator such as a centrifugal separator may optionally be used to remove trace amounts of liquid from the vapor phase.
• the vapor phase may be heated to above the flash temperature before entering the radiant section of the furnace, for example, to 425° C to 705° C (800° F to 1300° F). This heating may occur in a convection section tube bank, preferably the tube bank in the convection zone nearest the radiant section of the furnace.
• a transfer line exchanger can be used to produce high pressure steam which is then preferably superheated in a convection section tube bank of the pyrolysis furnace, typically to a temperature less than 590° C (1100° F), for example, 370° C to 565° C (700° F to 1050° F) by indirect contact with the flue gas before the flue gas enters the convection section tube bank used for heating the heavy hydrocarbon feedstock and/or mixture stream.
• An intermediate desuperheater may be used to control the temperature of the high pressure steam.
• the high pressure steam is preferably at a pressure of 4240 kPa (615 psia) or greater and may have a pressure of 10450 to 13900 kPa (1515 to 2015 psia).
• the high pressure steam superheater tube bank is preferably located in a convection zone between the first convection zone tube bank and the convection zone tube bank used for heating the vapor phase.
• the cooled gaseous effluent derived from the transfer line exchanger is directed to a recovery train for recovering C 2 to C 4 olefins, inter alia.
• a hydrocarbon feedstock 10 e.g., heavy crude oil requiring high preheat duties, or crude oil/condensate mixtures requiring low preheat duties
• a hydrocarbon feedstock e.g., heavy crude oil requiring high preheat duties, or crude oil/condensate mixtures requiring low preheat duties
• the initial feed temperature is measured at the heat exchanger inlet, and the feed temperature exiting the heat exchanger, is measured at the heat exchanger outlet.
• Preheated feed passes via line 14 into a first convection zone exchanger tube bank 15 in steam cracking furnace (pyro lysis reactor) 16 at the upper portion of convection section 18 for additional preheating.
• Heating of the feedstock within the convection section is by indirect contact of the feedstock in the convection section of the furnace, using hot flue gases from the radiant section 20 of the furnace exiting via furnace outlet 22 which can be associated with a blower 23 to vary draft as needed.
• the feedstock as measured at the outlet of the first convection zone exchanger tube bank in the upper convection section has a temperature between 100° C and 300° C (212° F and 572° F).
• the temperature of the heated feedstock is between 120° C and 270° C (248° F and 518° F), and most preferably between 130° C and 250° C (266° F and 482° F).
• the additionally preheated feedstock passes through a sparger 24 that receives water via line 26 controlled by valve 28 to introduce water or other suitable fluid to the feed.
• Dilution steam is introduced to the sparger via line 30 controlled by valve 32 where it mixes with the feedstock and water, the mixture exiting the sparger via line 34 which returns to an intermediate convection zone tube exchanger bank 35 for additional heating of the mixture which is taken outside the convection section via line 36 for reintroduction to the convection section for further heating in a lower intermediate convection zone tube bank.
• the mixture again exits the convection section, this time via line 38 to a vapor-liquid separator 40 through a side inlet 42.
• Liquid is taken as bottoms from the separator via bottom outlet 44 (at which point bottoms temperatures can be measured) via line 46 and then directed via pump 48 as heat transfer medium to heat exchanger 12.
• the liquid separator bottoms taken from the heat exchanger can be recycled via line 50, controlled by valve 52 to the boot 54 of the vapor-liquid separator. Unrecycled liquid bottoms are collected for liquid stream export via line 56 controlled by valve 58.
• Superheated dilution steam can be mixed with the feed to the vapor-liquid separator via line 64, intermediate convection zone tube exchanger bank 68, and line 70, controlled by valve 66.
• Desuperheating water can be mixed with the superheated dilution steam via line 60 controlled by valve 62.
• the heated dilution steam passes via line 70 to the vapor-liquid separator via line 38.
• the desuperheater maintains the temperature of the dilution steam between 425° C and 590° C (800° F and 1100° F), for example, between 455° C and 540° C (850° F and 1000° F), such as between 455° C and 510° C (850° F and 950° F), and typically between 470° C and 495° C (875° F and 925° F), as measured at the inlet to the vapor-liquid separator 40.
• the desuperheater can be a control valve and water atomizer nozzle.
• the vapor from the vapor-liquid separator 40 passes as overhead via line 72 to a downstream convection zone tube exchanger bank 79 where it is heated, and thence to crossover line 76 from which it is directed to the radiant section 20 from which it emerges as hot gaseous pyrolysis effluent.
• the hot gaseous pyrolysis effluent exits the radiant section 20 of steam cracking furnace 16 via line 78 into at least one primary transfer line heat exchanger 80 that cools the effluent from an inlet temperature ranging from 704° C to 927° C (1300° F and 1700° F), say, from 760° C to 871° C (1400° F to 1600° F), e.g., 816° C (1500° F), to an outlet temperature ranging from 316° C to 704° C (600° C to 1300° F), say, from 371° C to 649° C (700° F to 1200° F), e.g., 538° C (1000° F).
• High pressure boiler feed water can be directed via line 84 for preheating to a high pressure boiler feed water heat exchange coil 86 located below the intermediate convection zone tube exchanger bank coil 35 that receives sparger 24 effluent via line 34.
• the preheated high pressure boiler feed water is directed to a steam drum (not shown) via line 88.
• Alternate or additional heating of high pressure boiler feed water can be carried out by directing a source of high pressure boiler feed water 90 to a low temperature high pressure boiler feed water preheat coil 92 situated above the initial feed inlet to the furnace at the first convection zone heat exchanger tube bank 15.
• This preheated boiler feed water can be directed via line 94 to the high pressure boiler feed water heat exchange coil 86 for additional preheating as necessary.
• the use of the low temperature high pressure boiler feed water preheat coil 92 heat provides for efficient furnace operation for a wider variety of feed cases using heat from flue gas that would otherwise be vented to the atmosphere.
• Saturated high pressure steam is taken from a steam drum via line 96 to a high pressure steam heat exchange coil 98 located in a convection zone beneath high pressure boiler feed water heat exchange coil 86.
• the heated superheated high pressure steam is directed outside the convection section 18 via line 100 where desuperheater water can be added to the heated superheated high pressure steam via line 102 controlled by valve 104.
• the heated superheated high pressure steam having a pressure of at least 4100 kPa (600 psia) (or resulting mixture of steam and water) can be directed via line 100 for additional heating to a convection zone for secondary superheated high pressure steam heater 106 located below the lower intermediate convection zone tube bank 37 for heating.
• TABLE 1 illustrates the predicted performance of a furnace having the convection zones, vapor-liquid separator, and feed preheater/bottoms cooler arrangement shown in the FIGURE described above. The predicted performance is based upon a computer simulation.
• the present invention provides for a wide range of hydro carbonaceous feedstocks to be processed, such as crude oils and atmospheric resids, while minimizing the flow rate of water to the convection section, thereby reducing the energy inefficiencies and environmental treatment demands associated with the addition of fluids such as water to the steam cracking process.

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