US3849075A - Cracking reactor - Google Patents

Cracking reactor Download PDF

Info

Publication number
US3849075A
US3849075A US00359676A US35967673A US3849075A US 3849075 A US3849075 A US 3849075A US 00359676 A US00359676 A US 00359676A US 35967673 A US35967673 A US 35967673A US 3849075 A US3849075 A US 3849075A
Authority
US
United States
Prior art keywords
tube
ratio
orifice
walls
equivalent diameter
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US00359676A
Inventor
C Albright
G Keller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Priority to US00359676A priority Critical patent/US3849075A/en
Priority to FR7414938A priority patent/FR2229756A1/en
Priority to CA199,929A priority patent/CA1025640A/en
Priority to NL7406406A priority patent/NL7406406A/xx
Priority to JP5234374A priority patent/JPS5411282B2/ja
Priority to IT2264274A priority patent/IT1012311B/en
Priority to DE19742423143 priority patent/DE2423143A1/en
Priority to BE144240A priority patent/BE814934A/en
Application granted granted Critical
Publication of US3849075A publication Critical patent/US3849075A/en
Assigned to MORGAN GUARANTY TRUST COMPANY OF NEW YORK, AND MORGAN BANK ( DELAWARE ) AS COLLATERAL ( AGENTS ) SEE RECORD FOR THE REMAINING ASSIGNEES. reassignment MORGAN GUARANTY TRUST COMPANY OF NEW YORK, AND MORGAN BANK ( DELAWARE ) AS COLLATERAL ( AGENTS ) SEE RECORD FOR THE REMAINING ASSIGNEES. MORTGAGE (SEE DOCUMENT FOR DETAILS). Assignors: STP CORPORATION, A CORP. OF DE.,, UNION CARBIDE AGRICULTURAL PRODUCTS CO., INC., A CORP. OF PA.,, UNION CARBIDE CORPORATION, A CORP.,, UNION CARBIDE EUROPE S.A., A SWISS CORP.
Assigned to UNION CARBIDE CORPORATION, reassignment UNION CARBIDE CORPORATION, RELEASED BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: MORGAN BANK (DELAWARE) AS COLLATERAL AGENT
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/24Stationary reactors without moving elements inside
    • B01J19/2415Tubular reactors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/24Stationary reactors without moving elements inside
    • B01J19/2405Stationary reactors without moving elements inside provoking a turbulent flow of the reactants, such as in cyclones, or having a high Reynolds-number
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00051Controlling the temperature
    • B01J2219/00157Controlling the temperature by means of a burner
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00051Controlling the temperature
    • B01J2219/00159Controlling the temperature controlling multiple zones along the direction of flow, e.g. pre-heating and after-cooling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00164Controlling or regulating processes controlling the flow
    • B01J2219/00166Controlling or regulating processes controlling the flow controlling the residence time inside the reactor vessel
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/19Details relating to the geometry of the reactor
    • B01J2219/194Details relating to the geometry of the reactor round
    • B01J2219/1941Details relating to the geometry of the reactor round circular or disk-shaped
    • B01J2219/1942Details relating to the geometry of the reactor round circular or disk-shaped spherical
    • 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
    • C10G2400/00Products obtained by processes covered by groups C10G9/00 - C10G69/14
    • C10G2400/20C2-C4 olefins
    • 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
    • Y10S585/919Apparatus considerations
    • Y10S585/921Apparatus considerations using recited apparatus structure
    • Y10S585/924Reactor shape or disposition
    • 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
    • Y10S585/919Apparatus considerations
    • Y10S585/921Apparatus considerations using recited apparatus structure
    • Y10S585/924Reactor shape or disposition
    • Y10S585/925Dimension or proportion

Definitions

  • A. a circular convex lens shaped hollow structure having (i) two walls, which are joined at their peripheries to form the structure, at least one of said walls being provided with an orifice disposed substantially centrally, therein; and (ii) at least one hollow inlet feed chamber open at both ends passing through a wall of the structure, one end of said feed chamber being disposed in the interior of the structure at about the juncture of the walls in such a manner that vapor, which is passed through said chamber, will flow substantially tangentially to the juncture, provided that the rate of flow is sufficient therefor, creating a vortexrlike flow within the structure; and
  • one end of the tube is connected to the structure at its orifice in substantially concentric alignment therewith and in open communication with the structure;
  • the ratio of the length of the structure measured along a theoretical axis, which joins the center points of the walls, to the diameter of the structure measured across a theoretical plane perpendicular to the theoretical axis and bisecting the structure is about 0.05:1 to about 1:1;
  • the ratio of the equivalent diameter of the orifice of the structure to the equivalent diameter of the tube is about 1:1 to about 0.1:1.
  • the tube has a length to equivalent diameter ratio of about 5:1 to about 200:1;
  • the ratio of the volume of the structure to the volume of the tube is about 0.01:1 to about 5:1.
  • thermal cracking involves introducing liquid feedstocks into a reactor in atomized form together with superheated steam, and/or another hot gas, which supplies the heat necessary for the endothermic cracking reaction.
  • the introduction of the feedstocks and steam is accomplished in such a manner that the components are thoroughly mixed and the high temperature is uniformly and rapidly established throughout'the incoming feedstock.
  • An object of this invention is to provide a reactor which, using conventional processes, is capable of cracking a variety of hydrocarbon feedstocks,
  • A. a circular convex lens shaped hollow structure having (i) two walls, which are joined at their peripheries to form the structure, at least one of said walls being provided with an orifice disposed substantially cen trally therein; and (ii) at least one hollow inlet feed chamber open at both ends passing through a wall of the structure, one end of said feed chamber being disposed in the interior of the structure at about the juncture of the walls in such a manner that vapor, which is passed through said chamber, will flow substantially tangentially to the juncture, provided that the rate of flow is sufficient therefor, creating a vortex-like flow within the structure; and
  • one end of the tube is connected to the structure at its orifice in substantially concentric alignment therewith and in open communication with the structure;
  • the ratio of the length of the structure measured along a theoretical axis, which joins the center points of the walls, to the diameter of the structure measured across a theoretical plane perpendicular to the theoretical axis and bisecting the structure is about 0.05:1 to about 1:1;
  • the ratio of the equivalent diameter of the orifice of the structure to the equivalent diameter of the tube is about 0.121 to about 1:1;
  • the tube has a length to equivalent diameter ratio of about 5:1 to about 200:1;
  • FIG. 1 is a schematic sideview cross section of a reactor embodying the invention.
  • FIG. 2 is a schematic plan view taken along line 22 of FIG. 1.
  • FIG. 3 is a schematic plan view taken along line 3-3 of FIG. 1.
  • FIG. 4 is a schematic flow diagram illustrating a conventional system in which a reactor embodying the invention can be used.
  • the reactor can be made from various materials, the preferred material being stainless steel, e.g., AISI type 316 stainless steel.
  • Other representative materials from which the reactor can be made are AISI types 304 and 347 stainless steels; an alloy containing approximately 76 percent nickel, 16 percent chromium, and 6 percent iron; as well as various ceramics with high temperature stability.
  • the thickness of the reactor walls can be decided upon conventional lines and is not critical to the invention. Temperatures, pressures, longevity, economics,
  • the mixture enters inlet feed chamber 3 and then passes into interior 9 of the lens portion of the reactor where the cracking begins.
  • Inlet feed chamber (or inlet tube) 3 is disposed in interior 9 at the juncture of walls 4 and 12, which describe a convex lens type structure.
  • inlets There can be one or more inlets depending on the size of the reactor and the feed input per unit time desired, all placed in a similar manner to chamber 3, preferably at points equally spaced on either side from one another along the juncture at the peripheries of walls 4 and 12.
  • two inlets can be connected through the juncture at points representing 180 and 360, respectively; three inlets at points along the juncture representing 120, 240 and 360, respectively; and four inlets along the juncture at 90, 180, 270, and 360, respectively.
  • connection of chamber 3, and similar tubes, to the interior of the structure is preferably essentially tangential; however, such disposition is best defined by stating that it be disposed in such a manner that gas flowing from the chamber can flow substantially tangentially to the juncture of walls 4 and 12 creating a vortex-like flow in the lens portion of the reactor.
  • the size and shape of the chamber, the rate of flow of the feedstock/hot gas mixture, and the direction of flow will have to be considered by the technician in achieving tangential and vortex-like flow in the lens.
  • the inlet chamber is a tube with openings at both ends placed in a fixed position in the lens so that its theoretical axis is tangential to the juncture of the walls, in this case walls 4 and 12, and the rate of flow is controlled to achieve the tangential and vortex-like flow.
  • chamber 3 is preferably disposed through the juncture as shown in the drawing, it can be disposed through wall 4 or wall 12 and still achieve a modicum of tangential flow together with vortex-like flow. Although such a disposition is contemplated, it is not the preferred way of carrying out the invention in view of the irregularities of the flow.
  • Top wall 4 is a circular structure representing one half of the convex lens type structure and is the same shape as bottom wall 12. It has no openings except at the point where inlet feed chamber 3 is disposed.
  • the are described by wall 4 can be in the range of about 1 1 to about 124 and is preferably in the range of about 23 to about 106.
  • the definition of the arc is not critical because the dimensions of the lens are defined by various ratios mentioned heretofore.
  • bottom wall 12 is the mirror image of top wall 4 except for orifice 6 disposed substantially centrally therein.
  • the mixture which now comprises partially cracked feedstock, its cracked derivatives, and steam, and/or other hot gases, passes from the lens portion of the reactor through orifice 6 into interior 1]. of the hollow tube portion of the reactor.
  • Wall 5 describes the hollow tube of the tube portion which is open at both ends. The tube is in open communication with the lens through orifice 6.
  • Wall 5 can be connected to wall 12 at the boundaries of orifice 6 or, if the diameter of the tube is greater than the orifice, wall 5 can be connected at other points on wall 12. In any case, the center of the tube is substantially aligned with the center of the orifice.
  • the cross-section of the hollow tube can be of a variety of shapes, a cylindrical cross-section being preferred. It can, for example, be square, rectangular, triangular, pentagonal, hexagonal, or elliptical, although a mixture of these cross-sections in the same tube is not recommended.
  • the tube can also be a helical coil, which may be of value if the space available will not accommodate a straight tube.
  • the lens portion of the reactor will be referred to as structure A and the tube portion of the reactor as tube B.
  • the important dimensions are as follows:
  • c the equivalent diameter of tube B, the tube portion of the reactor. This dimension can also be referred to insofar as the drawing is concerned to the diameter of the cylindrical tube bounded by wall 5.
  • orifice 6 is not shown in the drawing since it coincides with dimension c. This dimension can, however, be different from dimension c and will be referred to hereinafter as the equivalent diameter of the orifice of structure A.
  • dimensions a, b, and c are outer dimensions which include the thickness of the reactor walls. This was an arbitrary selection, i.e., interior dimensions could have just as well been used.
  • Equivalent diameter is used to describe dimension c and the dimension of orifice 6 simply because the tube and orifice do not have to be cylindrical cross-sections, but can take on a variety of shapes. Various kinds of shapes were mentioned heretofore for the tube and this is applicable to the orifice also. Equivalent diameter is a convenient way of defining both non-cylindrical cross-sections and cylindrical cross-sections with one term. The mathematical abbreviation for equivalent diameter is D and the equation defining this term is as folows:
  • the ratio of the equivalent diameter of the orifice of structure A to the equivalent diameter of tube B can be in the range of about 1:1 to about 0.121 and is preferably in the range of about 1:1 to about 0.25:1.
  • Tube B can have a length d to equivalent diameter c ratio in the range of about 5:1 to about 200:1 and such ratio is preferably in the range of about :1 to about 100:1.
  • the ratio of the volume of structure A to the volume of tube B can be in the range of about 0.01:1 to about 5:1 and is preferably in the range of about 0.01:1 to about 2.5:1.
  • Volume of structure A is approximately defined by the following equation:
  • Volume 1/24 (11') (diameter)*] Volume of tube B is defined by the following equation:
  • volume (rr) [diameter or equivalent diameter/2] (length)
  • the actual dimensions of the reactor vary according to the use to which the reactor is to be put, e. g., laboratory, pilot plant, or commerical use and, even more so, according to the amount of throughput desired.
  • the number of inlet feed chambers, the number of tube portions, i.e., one or two, and the number of reactors along with many auxillary factors such as the particular economics of the situation must all be considered.
  • An illustration of the range of dimensions, which would be desirable for a feedstock throughput of 50 to 100 pounds per hour, using one inlet feed chamber and one tube portion, is as follows:
  • FIG. 4 is a schematic flow diagram illustrating a conventional system in which a reactor embodying the invention can be used.
  • Zone 21 represents the source of the feedstock and includes a preheating section where the feed is preheated to a temperature in the range of about 100C.
  • feedstocks such as pentanes and hexanes.
  • the preferred feedstocks in this system are naphtha, gas oil, and crude oil, the efficient cracking of which is an object of this invention.
  • gaseous feedstocks are natural gas, synthetic natural gas and various gaseous hydrocarbon components such as ethane, propane, and butanes.
  • the most noteworthy characteristic of the instant cracking reactor is its ability to accept and process high boiling fractions, which cannot be vaporized at 500C. at normal pressures. These fractions are, of course, major constituents of crude oil.
  • the feed passes along line 22, which corresponds to line 1 in FIG. 1, and joins line 23., which in part corresponds to line 2 in FIG. 1.
  • Line 23 is carrying a hot gas from zone 24 which represents a hot gas source.
  • the temperature of the hot gas is in the range of about l,000C. to about 3,000C. and is preferably in the range of about 1,200C. to about 2,500C.
  • the hot gases which can be used to crack the feedstock are exemplified by superheated steam, which is preferred, or products of combustion of various fuels.
  • the ratio of hot gas to feedstock lies in the range of about 0.5 parts by weight of hot gas per part by weight of feedstock to about 5 parts by weight of hot gas per part by weight of feedstock and! is preferably in the range of about 0.7 parts by weight of hot gas per part by weight of feedstock to about 2.5 parts by weight of hot gas per part by weight of feedstock.
  • the mixture of preheated feedstock and hot gas proceeds along line 25, which corresponds to the remaining length of line 2 in FIG. 1, into the reactor heretofore described.
  • Temperatures in the lens portion of the reactor are in the range of about 500C. to about 1,200C. and are preferably in the range of about 600C. to about 1,100C. Temperatures at the outlet of the tube portion of the reactor are in the range of about 45 0C. to about l,l50C. and are preferably in the range of about 550C. to about 1,050C.
  • Pressures are in the range of about 1 atmosphere to about 10 atmospheres and are preferably in the range of about 1 atmosphere to about 5 atmospheres.
  • Residence time is maintained within the range of about 0.005 seconds to about 0.5 seconds and is preferably in the range of about 0.01 seconds to about 0.2 seconds.
  • reactor effluent passes from reactor 26 along line 27 into quench zone 28.
  • Water or a hydrocarbon stream is used to quench the effluent. Separation of the effluent takes place in this zone with the gas product going overhead along line 29 and the water and liquid product being taken off as bottoms through line 30. Again, separation, recovery and analysis are conventional,
  • Another embodiment of the described reactor concerns the use of two tube portions connected to the lens portion in the same manner as the tube portion described above except that, in terms of FIG. 1, the connection would be to wall 4 at an orifice similar to orifice 6 disposed in that side. All ratios would be the same for this tube portion as for the tube portion heretofore described. The only change would be the step-up in rate of flow of feedstock and hot gas and the preferable use of multiple inlet feed chambers.
  • the outlets of both tube portions can be connected to one downstream system or two of such systems.
  • EXAMPLE 1 The system and reactor heretofore described are used in this example. More specifically, the procedure followed and the conditions used are as follows:
  • a steam generating system is started first by increasing natural gas flow to a furnace and turning on a water pump.
  • a high steam generation rate is used on startup to rapidly heat the associated piping.
  • the water rate is then adjusted to that required to meet test conditions. Approximately 1 hour is required for the steam generation conditions to stabilize after adjustment because of the large volume of the steam generating coils.
  • steam is turned into the mixing section to preheat the reaction system.
  • the burner and reactor When the burner and reactor are at or above the saturation steam temperature the burner is readied for ignition. Hydrogen is used as fuel for the burner. The burner and reactor are first purged with nitrogen to be sure no combustibles are present. The burner is then ignited. Hydrogen and oxygen flows to the burner are controlled in the proportion for proper combustion, both streams being increased simultaneously to raise the reactor temperature. The function of the burner is to provide a heat source to supply the required sensible heat and heat of reaction.
  • the feed pump When the reactor is heated almost to operating temperature, the feed pump is turned on.
  • the hydrocarbon feed is admitted near the outlet of the mixing section where it is mixed with the steam and the mixture passes into what is designated as inlet feed chamber 3 in FIGS. 1 and 2 of the drawing.
  • This inlet feed chamber 3 is attached so that its theoretical axis is tangential to the juncture of the walls of the lens portion of the reactor.
  • Reactor temperature, feed rate, water rate, and combustion rate are controlled to provide tangential flow of the feed/steam mixture and to give the desired residence time.
  • the reactor effluent is quenched with water to condense residual oils and a major proportion of the steam (about 80 percent by weight). Quench water rate is controlled to maintain the temperature of the stream leaving the quench zone at 70C.
  • the gaseous product leaving the quench zone or sep arator is cooled to ambient temperature in a condenser. Condensed hydrocarbons and water are collected and the make gas is flared.
  • the outer dimensions of the reactor used in this example are as follows:
  • the lens portion i.e., structure A, has a length of 2.625 inches and a diameter of 9 inches for a length to diameter ratio of 2.62519 or 0.29:1.
  • the tube portion i.e., tube B, is a helical coil of cylindrical cross-section having a length of 56 inches and a diameter of 1.5 inches for a length to diameter ratio of 56:1.5 or 37:1.
  • the volume of structure A is (n/24) (2.625) [(2.625 3(9) ]or 86 cubic inches.
  • the volume of tube (B) is (1r) (0.75) (56) or 99 cubic inches.
  • the ratio of the volume of tube A to the volume of tube B is, therefore, 86:99 or 0.87:1.
  • the total volume of structure A plus tube B is cubic inches or 3,034 cubic centimeters.
  • the ratio of the diameter of the orifice of structure A to the diameter of tube B, both of which are circular cross-sections, is 1:1.
  • the feedstock is designated as Texaco naphtha having the following analysis.
  • the reactor of this invention is considered especially degraded to a low molecular weight liquid wax-type or heavy oil-type composition, which can be cracked in subject reactor to ethylene yields approaching 60 percent or more.
  • a reactor adapted for the cracking of hydrocarbuns with hot gas comprising:
  • A. a circular convex lens shaped hollow structure having (i) two walls, which are joined at their peripheries to form the structure, at least one of said walls being provided with an orifice disposed substantially centrally therein; and (ii) at least one hollow inlet feed chamber open at both ends passing through a wall of the structure, one end of said feed chamber being disposed in the interior of the structure at about the juncture of the walls in such a manner that vapor, which is passed through said chamber, will flow substantially tangentially to the juncture, provided that the rate of flow is sufficient therefor, creating a vortex-like flow within the structure; and
  • tube (B) is connected to structure (A) at about its orifice in substantially concentric alignment therewith and in open communication with structure (A);
  • the ratio of the length of structure (A) measured along a theoretical axis, which joins the center points of the walls, to the diameter of structure (A) measured across a theoretical plane perpendicular to the theoretical axis and bisecting structure (A) is about 0.05:1 to about 1:1;
  • the ratio of the equivalent diameter of the orifice of structure (A) to the equivalent diameter of tube (B) is about 1:1 to about 0.1:1;
  • cl. tube (B) has a length to the equivalent diameter ratio of about 5:1 to about 200:1;
  • the ratio of the volume of structure (A) to the volume of tube (B) is about 0.01:1 to about 5:1.
  • structure (A) has a length to diameter ratio of about 0.1:1 to about 1:1;
  • the ratio of the equivalent diameter of the orifice of structure (A) to the equivalent diameter of tube (B) is about 1:1 to about 0.25:1;
  • d. tube (B) has a length to equivalent diameter ratio of about 10:1 to about :1;
  • the ratio of the volume of structure (A) to the volume of tube (B) is about 0.01:1 to about 2.5:1.
  • structure (A) has a length to diameter ratio of about 0.1:1 to about 1:1;
  • the ratio of the equivalent diameter of the orifice of structure (A) to the equivalent diameter of tube (B) is about 1:1 to about 0.25:1;
  • (1. tube (B) has a length to equivalent diameter ratio of about 10:1 to about 100:1;
  • the ratio of the volume of structure (A) to the volume of tube (B) is about 0.01:1 to about 2.5:1.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A reactor adapted for the cracking of hydrocarbons with hot gas comprising: A. a circular convex lens shaped hollow structure having (i) two walls, which are joined at their peripheries to form the structure, at least one of said walls being provided with an orifice disposed substantially centrally therein; and (ii) at least one hollow inlet feed chamber open at both ends passing through a wall of the structure, one end of said feed chamber being disposed in the interior of the structure at about the juncture of the walls in such a manner that vapor, which is passed through said chamber, will flow substantially tangentially to the juncture, provided that the rate of flow is sufficient therefor, creating a vortex-like flow within the structure; and B. at least one hollow tube open at both ends; WHEREIN: A. ONE END OF THE TUBE IS CONNECTED TO THE STRUCTURE AT ITS ORIFICE IN SUBSTANTIALLY CONCENTRIC ALIGNMENT THEREWITH AND IN OPEN COMMUNICATION WITH THE STRUCTURE; B. THE RATIO OF THE LENGTH OF THE STRUCTURE MEASURED ALONG A THEORETICAL AXIS, WHICH JOINS THE CENTER POINTS OF THE WALLS, TO THE DIAMETER OF THE STRUCTURE MEASURED ACROSS A THEORETICAL PLANE PERPENDICULAR TO THE THEORETICAL AXIS AND BISECTING THE STRUCTURE IS ABOUT 0.05:1 TO ABOUT 1:1; C. THE RATIO OF THE EQUIVALENT DIAMETER OF THE ORIFICE OF THE STRUCTURE TO THE EQUIVALENT DIAMETER OF THE TUBE IS ABOUT 1:1 TO ABOUT 0.1:1. D. THE TUBE HAS A LENGTH TO EQUIVALENT DIAMETER RATIO OF ABOUT 5:1 TO ABOUT 200:1; AND E. THE RATIO OF THE VOLUME OF THE STRUCTURE TO THE VOLUME OF THE TUBE IS ABOUT 0.01:1 TO ABOUT 5:1.

Description

United States Patent [191 Albright et ai.
[ CRACKING REACTOR [75] Inventors: Charles W. Albright; George E.
Keller, 11, both of South Charleston, W. Va.
[73] Assignee: Union Carbide Corporation, New
York, NY.
[22] Filed: May 14, 1973 [21] Appl. No.: 359,676
Related 1.1.8. Application Data [63] Continuation-impart of Ser. No. 252,512, May 8,
1972, abandoned.
[52] 0.8. Ci. 23/284, 23/252 R, 23/277 R, 259/4, 260/679 R, 260/683 R [51] Int. Cl 801i 3/04, B01j 1/00, C07c 11/04 [58] Field of Search 23/284, 285, 277 R, 252 R, 23/277 C; 260/677 R, 679 R, 683 R, 678; 196/115, 123, 126, 129; 48/94, 75, 105; 259/4 [56] References Cited UNITED STATES PATENTS 3,351,427 11/1967 Wendell et al. 23/277 R X 3,498,753 3/1970 Hokari et al 23/284 X 3,563,710 2/1971 Dew, Jr. et al. 23/285 Primary Examiner-Joseph Scovronek Attorney, Agent, or Firm-Saul R. Bresch with hot gas comprising:
A. a circular convex lens shaped hollow structure having (i) two walls, which are joined at their peripheries to form the structure, at least one of said walls being provided with an orifice disposed substantially centrally, therein; and (ii) at least one hollow inlet feed chamber open at both ends passing through a wall of the structure, one end of said feed chamber being disposed in the interior of the structure at about the juncture of the walls in such a manner that vapor, which is passed through said chamber, will flow substantially tangentially to the juncture, provided that the rate of flow is sufficient therefor, creating a vortexrlike flow within the structure; and
B. at least one hollow tube open at both ends;
wherein:
a. one end of the tube is connected to the structure at its orifice in substantially concentric alignment therewith and in open communication with the structure;
b. the ratio of the length of the structure measured along a theoretical axis, which joins the center points of the walls, to the diameter of the structure measured across a theoretical plane perpendicular to the theoretical axis and bisecting the structure is about 0.05:1 to about 1:1;
c. the ratio of the equivalent diameter of the orifice of the structure to the equivalent diameter of the tube is about 1:1 to about 0.1:1.
, d. the tube has a length to equivalent diameter ratio of about 5:1 to about 200:1; and
e. the ratio of the volume of the structure to the volume of the tube is about 0.01:1 to about 5:1.
7 Claims, 4 Drawing; Figures @1 t a 2 a 1 w 1 N I? z \i b CRACKING REACTOR FIELD OF THE INVENTION This invention relates to an improvement in the systems presently used for the thermal cracking of hydrocarbons with hot gases and more particularly, to an improved cracking reactor for such systems.
DESCRIPTION OF THE PRIOR ART Thermal cracking of hydrocarbon feedstocks has for many. years been a major source for supplying the needs of the chemical industry with the most basic of chemicals such as ethylene and propylene, the former being used chiefly in the production of low and high density polyethylene, ethylene oxide and vinyl chloride, and the latter for the production of isopropyl alcohol, acrylonitrile, polypropylene and propylene oxide.
Natural gas or. various components thereof and naphtha are currently the major feedstocks from which ethylene, propylene and acetylene are derived by thermal cracking; however, shortages of these feedstocks at reasonable cost suggest that industry will have to turn to crude oil or even heavier materials in their stead. One method for thermal cracking involves introducing liquid feedstocks into a reactor in atomized form together with superheated steam, and/or another hot gas, which supplies the heat necessary for the endothermic cracking reaction. The introduction of the feedstocks and steam is accomplished in such a manner that the components are thoroughly mixed and the high temperature is uniformly and rapidly established throughout'the incoming feedstock.
The main drawbacks in present thermal cracking techniques center in the reactors available in that they are not versatile, i.e., these reactors do not accept a variety of liquid feedstocks such as naphtha, gas oils, natural gasolines, raffinates, and their component hydrocarbons, which are being used as feedstocks and will continue to be used for many years, together with crude oil and possibly even heavier materials, which will be used more and more in the future, and present reactors do not have the capability of providing high yields of ethylene, propylene and acetylene regardless of the choice of feedstock. This simply means that because of the transitional nature of the economics affecting feedstocks, highly specialized reactors, which only accept limited kinds of feedstocks are not presently attractive investment-wise. Rather, to be commercially advantageous, a reactor must have sufficient flexibility to accept the feedstocks which are considered to be the most economic at the time whether, e.g., it is naphtha or crude oil, and provide good yields from either.
To date, the provision of high yield reactors for thermally cracking a variety of liquid feedstocks, all at high yields, has proved elusive especially when both naphtha and crude oil must be included in their repertoire.
SUMMARY OF THE INVENTION An object of this invention, therefore, is to provide a reactor which, using conventional processes, is capable of cracking a variety of hydrocarbon feedstocks,
particularly naphtha and crude oil, to ethylene, propylene and acetylene in high yield.
Other objects and advantages will become apparent hereinafter.
According to the present invention, such a reactor has been discovered for the cracking of hydrocarbons with hot gas comprising:
A. a circular convex lens shaped hollow structure having (i) two walls, which are joined at their peripheries to form the structure, at least one of said walls being provided with an orifice disposed substantially cen trally therein; and (ii) at least one hollow inlet feed chamber open at both ends passing through a wall of the structure, one end of said feed chamber being disposed in the interior of the structure at about the juncture of the walls in such a manner that vapor, which is passed through said chamber, will flow substantially tangentially to the juncture, provided that the rate of flow is sufficient therefor, creating a vortex-like flow within the structure; and
B. at least one hollow tube open at both ends; wherein:
a. one end of the tube is connected to the structure at its orifice in substantially concentric alignment therewith and in open communication with the structure;
b. the ratio of the length of the structure measured along a theoretical axis, which joins the center points of the walls, to the diameter of the structure measured across a theoretical plane perpendicular to the theoretical axis and bisecting the structure is about 0.05:1 to about 1:1;
c. the ratio of the equivalent diameter of the orifice of the structure to the equivalent diameter of the tube is about 0.121 to about 1:1;
(1. the tube has a length to equivalent diameter ratio of about 5:1 to about 200:1; and
e. the ratio of the volume of the structure to the volume of the tube is about 0.01:1 to about 5:1.
BRIEF DESCRIPTION OF THE DRAWING FIG. 1 is a schematic sideview cross section of a reactor embodying the invention.
FIG. 2 is a schematic plan view taken along line 22 of FIG. 1.
FIG. 3 is a schematic plan view taken along line 3-3 of FIG. 1.
It should be noted that the relative dimensions of parts of the reactor in FIGS. 1 to 3 do not conform to the ratios prescribed in the specification.
FIG. 4 is a schematic flow diagram illustrating a conventional system in which a reactor embodying the invention can be used.
DESCRIPTION OF THE PREFERRED EMBODIMENT The reactor can be made from various materials, the preferred material being stainless steel, e.g., AISI type 316 stainless steel. Other representative materials from which the reactor can be made are AISI types 304 and 347 stainless steels; an alloy containing approximately 76 percent nickel, 16 percent chromium, and 6 percent iron; as well as various ceramics with high temperature stability.
The thickness of the reactor walls can be decided upon conventional lines and is not critical to the invention. Temperatures, pressures, longevity, economics,
and available materials should be considered when parts of the reactor. The mixture enters inlet feed chamber 3 and then passes into interior 9 of the lens portion of the reactor where the cracking begins.
Inlet feed chamber (or inlet tube) 3 is disposed in interior 9 at the juncture of walls 4 and 12, which describe a convex lens type structure.
There can be one or more inlets depending on the size of the reactor and the feed input per unit time desired, all placed in a similar manner to chamber 3, preferably at points equally spaced on either side from one another along the juncture at the peripheries of walls 4 and 12. Thus, two inlets can be connected through the juncture at points representing 180 and 360, respectively; three inlets at points along the juncture representing 120, 240 and 360, respectively; and four inlets along the juncture at 90, 180, 270, and 360, respectively.
The connection of chamber 3, and similar tubes, to the interior of the structure is preferably essentially tangential; however, such disposition is best defined by stating that it be disposed in such a manner that gas flowing from the chamber can flow substantially tangentially to the juncture of walls 4 and 12 creating a vortex-like flow in the lens portion of the reactor. The size and shape of the chamber, the rate of flow of the feedstock/hot gas mixture, and the direction of flow will have to be considered by the technician in achieving tangential and vortex-like flow in the lens. In practice, the inlet chamber is a tube with openings at both ends placed in a fixed position in the lens so that its theoretical axis is tangential to the juncture of the walls, in this case walls 4 and 12, and the rate of flow is controlled to achieve the tangential and vortex-like flow.
Although chamber 3 is preferably disposed through the juncture as shown in the drawing, it can be disposed through wall 4 or wall 12 and still achieve a modicum of tangential flow together with vortex-like flow. Although such a disposition is contemplated, it is not the preferred way of carrying out the invention in view of the irregularities of the flow.
Top wall 4 is a circular structure representing one half of the convex lens type structure and is the same shape as bottom wall 12. It has no openings except at the point where inlet feed chamber 3 is disposed. The are described by wall 4 can be in the range of about 1 1 to about 124 and is preferably in the range of about 23 to about 106. The definition of the arc is not critical because the dimensions of the lens are defined by various ratios mentioned heretofore.
Since symmetry in the lens portion of the reactor is important, bottom wall 12 is the mirror image of top wall 4 except for orifice 6 disposed substantially centrally therein.
The mixture, which now comprises partially cracked feedstock, its cracked derivatives, and steam, and/or other hot gases, passes from the lens portion of the reactor through orifice 6 into interior 1]. of the hollow tube portion of the reactor. Wall 5 describes the hollow tube of the tube portion which is open at both ends. The tube is in open communication with the lens through orifice 6. Wall 5 can be connected to wall 12 at the boundaries of orifice 6 or, if the diameter of the tube is greater than the orifice, wall 5 can be connected at other points on wall 12. In any case, the center of the tube is substantially aligned with the center of the orifice.
The cross-section of the hollow tube can be of a variety of shapes, a cylindrical cross-section being preferred. It can, for example, be square, rectangular, triangular, pentagonal, hexagonal, or elliptical, although a mixture of these cross-sections in the same tube is not recommended. The tube can also be a helical coil, which may be of value if the space available will not accommodate a straight tube. The end of the tube opposite to the tubes connection to the disc at orifice 6 is outlet 7 through which the reactor is in open communication with the down-stream portion of the system and, after cracking is essentially completed in the tube portion, the effluent proceeds through this outlet.
Certain ratios concerning dimensions and volumes are critical to the invention. For the purpose of setting out these ratios, the lens portion of the reactor will be referred to as structure A and the tube portion of the reactor as tube B. The important dimensions are as follows:
a the diameter of structure A measured across a theoretical plane perpendicular to the theoretical axis joining the center points of walls 4 and 12, and bisecting the structure.
b the length of structure A measured along a theoretical axis, which joins the center points of walls 4 and 12.
c= the equivalent diameter of tube B, the tube portion of the reactor. This dimension can also be referred to insofar as the drawing is concerned to the diameter of the cylindrical tube bounded by wall 5.
d the length of tube B. This dimension can also be referred to as the height of wall 5.
The dimension of orifice 6 is not shown in the drawing since it coincides with dimension c. This dimension can, however, be different from dimension c and will be referred to hereinafter as the equivalent diameter of the orifice of structure A.
It should be noted that dimensions a, b, and c are outer dimensions which include the thickness of the reactor walls. This was an arbitrary selection, i.e., interior dimensions could have just as well been used.
Equivalent diameter is used to describe dimension c and the dimension of orifice 6 simply because the tube and orifice do not have to be cylindrical cross-sections, but can take on a variety of shapes. Various kinds of shapes were mentioned heretofore for the tube and this is applicable to the orifice also. Equivalent diameter is a convenient way of defining both non-cylindrical cross-sections and cylindrical cross-sections with one term. The mathematical abbreviation for equivalent diameter is D and the equation defining this term is as folows:
D (4 X cross-sectional area)/perimeter of crosssectional area Where the cross-sectional area of the tube varies along its length an average equivalent diameter can be used, but tubes of varying cross-section are considered impractical and are not recommended. The shape of the orifice can be different from that of the tube, how- 2. The ratio of the equivalent diameter of the orifice of structure A to the equivalent diameter of tube B can be in the range of about 1:1 to about 0.121 and is preferably in the range of about 1:1 to about 0.25:1.
3. Tube B can have a length d to equivalent diameter c ratio in the range of about 5:1 to about 200:1 and such ratio is preferably in the range of about :1 to about 100:1.
4. The ratio of the volume of structure A to the volume of tube B can be in the range of about 0.01:1 to about 5:1 and is preferably in the range of about 0.01:1 to about 2.5:1.
Volume of structure A is approximately defined by the following equation:
Volume 1/24 (11') (diameter)*] Volume of tube B is defined by the following equation:
Volume (rr) [diameter or equivalent diameter/2] (length) The actual dimensions of the reactor vary according to the use to which the reactor is to be put, e. g., laboratory, pilot plant, or commerical use and, even more so, according to the amount of throughput desired. The number of inlet feed chambers, the number of tube portions, i.e., one or two, and the number of reactors along with many auxillary factors such as the particular economics of the situation must all be considered. An illustration of the range of dimensions, which would be desirable for a feedstock throughput of 50 to 100 pounds per hour, using one inlet feed chamber and one tube portion, is as follows:
(length) [(length) +3- dimension value in inches a 7 to l2 b 2.2 to 3.0 c 1 to 2 d 30 to 70 of orifice 0.5 to 2 As stated heretofore, FIG. 4 is a schematic flow diagram illustrating a conventional system in which a reactor embodying the invention can be used.
Referring to FIG. 4 of the drawing:
Zone 21 represents the source of the feedstock and includes a preheating section where the feed is preheated to a temperature in the range of about 100C.
to about 700C. and preferably in the range of about such feedstocks such as pentanes and hexanes. The preferred feedstocks in this system are naphtha, gas oil, and crude oil, the efficient cracking of which is an object of this invention. Examples of gaseous feedstocks are natural gas, synthetic natural gas and various gaseous hydrocarbon components such as ethane, propane, and butanes.
The most noteworthy characteristic of the instant cracking reactor is its ability to accept and process high boiling fractions, which cannot be vaporized at 500C. at normal pressures. These fractions are, of course, major constituents of crude oil.
The feed passes along line 22, which corresponds to line 1 in FIG. 1, and joins line 23., which in part corresponds to line 2 in FIG. 1. Line 23 is carrying a hot gas from zone 24 which represents a hot gas source. The temperature of the hot gas is in the range of about l,000C. to about 3,000C. and is preferably in the range of about 1,200C. to about 2,500C. The hot gases which can be used to crack the feedstock are exemplified by superheated steam, which is preferred, or products of combustion of various fuels.
, The ratio of hot gas to feedstock lies in the range of about 0.5 parts by weight of hot gas per part by weight of feedstock to about 5 parts by weight of hot gas per part by weight of feedstock and! is preferably in the range of about 0.7 parts by weight of hot gas per part by weight of feedstock to about 2.5 parts by weight of hot gas per part by weight of feedstock.
The mixture of preheated feedstock and hot gas proceeds along line 25, which corresponds to the remaining length of line 2 in FIG. 1, into the reactor heretofore described.
Cracking is effected in subject reactor under the following conditions:
Temperatures in the lens portion of the reactor are in the range of about 500C. to about 1,200C. and are preferably in the range of about 600C. to about 1,100C. Temperatures at the outlet of the tube portion of the reactor are in the range of about 45 0C. to about l,l50C. and are preferably in the range of about 550C. to about 1,050C.
Pressures are in the range of about 1 atmosphere to about 10 atmospheres and are preferably in the range of about 1 atmosphere to about 5 atmospheres.
Residence time is maintained within the range of about 0.005 seconds to about 0.5 seconds and is preferably in the range of about 0.01 seconds to about 0.2 seconds.
The reactor effluent passes from reactor 26 along line 27 into quench zone 28. Water or a hydrocarbon stream is used to quench the effluent. Separation of the effluent takes place in this zone with the gas product going overhead along line 29 and the water and liquid product being taken off as bottoms through line 30. Again, separation, recovery and analysis are conventional,
The prior discussion has considered the use of both liquid and gaseous feedstocks in the above described reactor. its versatility goes beyond these feedstocks, however, e.g., oxygenated materials such as alcohols and acids, various polymeric materials, and Diels-Alder products can also be effectively cracked therein.
Another embodiment of the described reactor, concerns the use of two tube portions connected to the lens portion in the same manner as the tube portion described above except that, in terms of FIG. 1, the connection would be to wall 4 at an orifice similar to orifice 6 disposed in that side. All ratios would be the same for this tube portion as for the tube portion heretofore described. The only change would be the step-up in rate of flow of feedstock and hot gas and the preferable use of multiple inlet feed chambers. The outlets of both tube portions can be connected to one downstream system or two of such systems.
The following examples illustrate the invention. Parts and percentages are by weight unless otherwise designated.
EXAMPLE 1 The system and reactor heretofore described are used in this example. More specifically, the procedure followed and the conditions used are as follows:
Initially, a steam generating system is started first by increasing natural gas flow to a furnace and turning on a water pump. A high steam generation rate is used on startup to rapidly heat the associated piping. The water rate is then adjusted to that required to meet test conditions. Approximately 1 hour is required for the steam generation conditions to stabilize after adjustment because of the large volume of the steam generating coils. When the steam generation system is at the desired conditions, steam is turned into the mixing section to preheat the reaction system.
When the burner and reactor are at or above the saturation steam temperature the burner is readied for ignition. Hydrogen is used as fuel for the burner. The burner and reactor are first purged with nitrogen to be sure no combustibles are present. The burner is then ignited. Hydrogen and oxygen flows to the burner are controlled in the proportion for proper combustion, both streams being increased simultaneously to raise the reactor temperature. The function of the burner is to provide a heat source to supply the required sensible heat and heat of reaction.
When the reactor is heated almost to operating temperature, the feed pump is turned on. The hydrocarbon feed is admitted near the outlet of the mixing section where it is mixed with the steam and the mixture passes into what is designated as inlet feed chamber 3 in FIGS. 1 and 2 of the drawing. This inlet feed chamber 3 is attached so that its theoretical axis is tangential to the juncture of the walls of the lens portion of the reactor. Reactor temperature, feed rate, water rate, and combustion rate are controlled to provide tangential flow of the feed/steam mixture and to give the desired residence time.
The reactor effluent is quenched with water to condense residual oils and a major proportion of the steam (about 80 percent by weight). Quench water rate is controlled to maintain the temperature of the stream leaving the quench zone at 70C.
The gaseous product leaving the quench zone or sep arator is cooled to ambient temperature in a condenser. Condensed hydrocarbons and water are collected and the make gas is flared.
Analysis of the products is by gas chromatography and Mass Spectrometer gas analysis.
The outer dimensions of the reactor used in this example are as follows:
The lens portion, i.e., structure A, has a length of 2.625 inches and a diameter of 9 inches for a length to diameter ratio of 2.62519 or 0.29:1.
The tube portion, i.e., tube B, is a helical coil of cylindrical cross-section having a length of 56 inches and a diameter of 1.5 inches for a length to diameter ratio of 56:1.5 or 37:1.
The volume of structure A is (n/24) (2.625) [(2.625 3(9) ]or 86 cubic inches.
The volume of tube (B) is (1r) (0.75) (56) or 99 cubic inches.
The ratio of the volume of tube A to the volume of tube B is, therefore, 86:99 or 0.87:1.
The total volume of structure A plus tube B is cubic inches or 3,034 cubic centimeters.
The ratio of the diameter of the orifice of structure A to the diameter of tube B, both of which are circular cross-sections, is 1:1.
The feedstock is designated as Texaco naphtha having the following analysis.
Mass Spectrometer Analysis Normal Paraffins 39.49 percent [so Paraffins 38.61 percent Olefins 1.36 percent Napthenes 13.39 percent Aromatics 7.16 percent ASTM Distillation (ASTM No. D-86) Percent overhead Temperature (F.)
104 (initial boiling mol ratio Operating Conditions: Reactor temperature: 860C. at outlet of tube portion 2.] parts of steam per one part of feed 0047 62.5 pounds per hour 134 pounds per hour 10 pounds per square inch gauge Steam dilution ratio (by weight):
Residence time (seconds): rate of hydrocarbon feed: rate of steam feed: reactor pressure:
Results:
Yield in percent by weight ethylene propylene acetylene methane total gas product 011 coke EXAMPLE 2 Example 1 is repeated except that the feedstock is changed to that designated as Pennsylvania crude oil having the following analysis:
ASTM Distillation (ASTM No. D-86) Percent overhead Temperature (C.)
148 10 230 5 20 282 30 336 40 398 50 470 60 552 70 596 End point 596 Recovery 71 percent residue: 29 millimeters API Gravity: 46.6 at 60F. Specific Gravity: 0.795 at 60F. Refractive Index: 1.4412 at 20C. ppm sulfur: 1S3 bromine number: 2.]4 H/C, calculated from elemental analysis: 2.08 APl American Petroleum Institute ppm parts per million H/C hydlrogemcarbon mo ratio and various operating conditions are changed as follows:
Reactor temperature:
disc temperature 875C. outlet temperature (tube portion) 857C. Residence time (seconds): 0.040 rate of hydrocarbon feed: 74.1 pounds per hour molecular 'weight of feed: 180 rate of steam feed: 156 pounds per hour Results: Yield in percent by weight ethylene 38.4 propylene l 3.2 acetylene 1.8 methane 12.7 total gas product 84.2 oil coke 15.8
The reactor of this invention is considered especially degraded to a low molecular weight liquid wax-type or heavy oil-type composition, which can be cracked in subject reactor to ethylene yields approaching 60 percent or more.
What is claimed is:
l. A reactor adapted for the cracking of hydrocarbuns with hot gas comprising:
A. a circular convex lens shaped hollow structure having (i) two walls, which are joined at their peripheries to form the structure, at least one of said walls being provided with an orifice disposed substantially centrally therein; and (ii) at least one hollow inlet feed chamber open at both ends passing through a wall of the structure, one end of said feed chamber being disposed in the interior of the structure at about the juncture of the walls in such a manner that vapor, which is passed through said chamber, will flow substantially tangentially to the juncture, provided that the rate of flow is sufficient therefor, creating a vortex-like flow within the structure; and
B. at least one hollow tube open. at both ends; wherein:
a. one end of tube (B) is connected to structure (A) at about its orifice in substantially concentric alignment therewith and in open communication with structure (A);
b. the ratio of the length of structure (A) measured along a theoretical axis, which joins the center points of the walls, to the diameter of structure (A) measured across a theoretical plane perpendicular to the theoretical axis and bisecting structure (A) is about 0.05:1 to about 1:1;
0. the ratio of the equivalent diameter of the orifice of structure (A) to the equivalent diameter of tube (B) is about 1:1 to about 0.1:1;
cl. tube (B) has a length to the equivalent diameter ratio of about 5:1 to about 200:1; and
e. the ratio of the volume of structure (A) to the volume of tube (B) is about 0.01:1 to about 5:1.
2. The reactor defined in claim 1 wherein one wall is provided with the orifice and there is one tube (B) connected to structure (A) at about said orifice.
3. The reactor defined in claim 11 wherein both walls are provided with an orifice and two tubes (B) are connected to structure (A), one tube (B) at about each orifice.
4. The reactor defined in claim 2 wherein:
b. structure (A) has a length to diameter ratio of about 0.1:1 to about 1:1;
c. the ratio of the equivalent diameter of the orifice of structure (A) to the equivalent diameter of tube (B) is about 1:1 to about 0.25:1;
d. tube (B) has a length to equivalent diameter ratio of about 10:1 to about :1; and
e. the ratio of the volume of structure (A) to the volume of tube (B) is about 0.01:1 to about 2.5:1.
5. The reactor defined in claim 3 wherein:
b. structure (A) has a length to diameter ratio of about 0.1:1 to about 1:1;
c. the ratio of the equivalent diameter of the orifice of structure (A) to the equivalent diameter of tube (B) is about 1:1 to about 0.25:1;
(1. tube (B) has a length to equivalent diameter ratio of about 10:1 to about 100:1; and
e. the ratio of the volume of structure (A) to the volume of tube (B) is about 0.01:1 to about 2.5:1.
6. The reactor defined in claim 2 wherein the inlet feed chamber is a cylindrical tube, the theoretical axis of which is in essentially tangential alignment with the juncture of the walls of structure (A).
7. The reactor defined in claim 4 wherein the inlet feed chamber is a cylindrical tube, the theoretical axis of which is in essentially tangential alignment with the juncture of the walls of structure (A).
* a a: 1: a

Claims (7)

1. A REACTOR ADAPTED FOR THE CRACKING OF HYDROCARBONS WITH HOT GAS COMPRISING: A. A CIRCULAR CONVEX LES SHAPED HOLLOW STRUCTURE HAVING (I) TWO WALLS, WHICH ARE JOINED AT THEIR PERIPHERIES TO FORM THE STRUCTURE, AT LEAST ONE OF SAID WALLS BEING PROVIDED WITH AN ORIFICE DISPOSED SUBSTANTIALLY CENTRALLY THEREIN; AND (ii9 AT LEAST ONE HOLLOW INLET FEED CHAMBER OPEN AT BOTH ENDS PASSING THROUGH A WALL OF THE STRUCTURE, ONE END OF SAID FEED CHAMBER BEING DISPOSED IN THE INTERIOR OF THE STRUCTURE AT ABOUT THE JUNCTURE OF THE WALLS IN SUCH A MANNER THAT VAPOR, WHICH IS PASSED THROUGH SAID CHAMBER, WILL FLOW SUBSTANTIALLY TANGENTIALLY TO THE JUNCTURE, PROVIDED THAT THE RATE OF FLOW IS SUFFICIENT THEREFOR, CREATING A VORTEX-LIKE FLOW WITHIN THE STRUCTURE; AND B. AT LEAST ONE HOLLOW TUBE OPEN AT BOTH ENDS; WHEREIN; A. ONE END OF TUBE (B) IS CONNECED TO STRUCTURE (A) AT ABOUT ITS ORIFICE IN SUBSTANTIALLY CONCENTRIC ALIGNMENT THEREWITH AND IN OPEN COMMUNICATION WITH STRUCTURE (A); B. THE RATIO OF THE LENGTH OF STRUCTURE (A) MEASURED ALONG A THEORETICAL AXIS, WHICH JOINS THE CENTER POINTS OF THE WALLS, TO THE DIAMETER OF STRUCTURE (A) MEASURED ACROSS A THEORETICAL PLANE PERPENDICULAR TO THE THEORETICAL AXIS AND BISECTING STRUCTURE (A) IS ABOUT 0.05:1 TO ABOUT 1:1:. C. THE RATIO OF THE EQUIVALENT DIAMETER OF THE ORIFICE OF STRUCTRUE (A) TO THE EQUIVALENT DIAMTER OF THE TUBE (B) IS ABOUT 1:1 TO ABOUT 0.1:1. D. TUBE (B) HAS A LENGTH TO THE EQUIVALENT DIAMETER OF RATIO OF ABOUT 5:1 TO ABOUT 200:1. AND E. THE RATIO OF THE VOLUME OF STRUCTURE OF (A) TO THE VOLUME OF TUBE (B) IS ABOUT 0.01:1 TO ABOUT 5:1.
2. The reactor defined in claim 1 wherein one wall is provided with the orifice and there is one tube (B) connected to structure (A) at about said orifice.
3. The reactor defined in claim 1 wherein both walls are provided with an orifice and two tubes (B) are connected to structure (A), one tube (B) at about each orifice.
4. The reactor defined in claim 2 wherein: b. structure (A) has a length to diameter ratio of about 0.1:1 to about 1:1; c. the ratio of the equivalent diameter of the orifice of structure (A) to the equivalent diameter of tube (B) is about 1:1 to about 0.25:1; d. tube (B) has a length to equivalent diameter ratio of about 10:1 to about 100:1; and e. the ratio of the volume of structure (A) to the volume of tube (B) is about 0.01:1 to about 2.5:1.
5. The reactor defined in claim 3 wherein: b. structure (A) has a length to diameter ratio of about 0.1:1 to about 1:1; c. the ratio of the equivalent diameter of the orifice of structure (A) to the equivalent diameter of tube (B) is about 1:1 to about 0.25:1; d. tube (B) has a length to equivalent diameter ratio of about 10:1 to about 100:1; and e. the ratio of the volume of structure (A) to the volume of tube (B) is about 0.01:1 to about 2.5:1.
6. The reactor defined in claim 2 wherein the inlet feed chamber is a cylindrical tube, the theoretical axis of which is in essentially tangential alignment with the juncture of the walls of structure (A).
7. The reactor defined in claim 4 wherein the inlet feed chamber is a cylindrical tube, the theoretical axis of which is in essentially tangential alignment with the juncture of the walls of structure (A).
US00359676A 1972-05-08 1973-05-14 Cracking reactor Expired - Lifetime US3849075A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
US00359676A US3849075A (en) 1972-05-08 1973-05-14 Cracking reactor
FR7414938A FR2229756A1 (en) 1973-05-14 1974-04-30 Hydrocarbon cracker using hot gases - for naphtha, gas oil or crude feedstock
NL7406406A NL7406406A (en) 1973-05-14 1974-05-13
JP5234374A JPS5411282B2 (en) 1973-05-14 1974-05-13
CA199,929A CA1025640A (en) 1973-05-14 1974-05-13 Advanced cracking reactor
IT2264274A IT1012311B (en) 1973-05-14 1974-05-13 PERFECTED CRACKING REACTOR
DE19742423143 DE2423143A1 (en) 1973-05-14 1974-05-13 REACTOR FOR CRACKING HYDROCARBONS WITH HOT GAS
BE144240A BE814934A (en) 1973-05-14 1974-05-13 HYDROCARBON CRACKING REACTOR

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US25251272A 1972-05-08 1972-05-08
US00359676A US3849075A (en) 1972-05-08 1973-05-14 Cracking reactor

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
US05252511 Continuation-In-Part 1972-05-08
US25251272A Continuation-In-Part 1972-05-08 1972-05-08

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US05/498,990 Continuation-In-Part US3985820A (en) 1973-05-14 1974-08-20 Cracking process

Publications (1)

Publication Number Publication Date
US3849075A true US3849075A (en) 1974-11-19

Family

ID=26942380

Family Applications (1)

Application Number Title Priority Date Filing Date
US00359676A Expired - Lifetime US3849075A (en) 1972-05-08 1973-05-14 Cracking reactor

Country Status (1)

Country Link
US (1) US3849075A (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4005986A (en) * 1972-11-06 1977-02-01 Nippon Kokan Kabushiki Kaisha Device for making high temperature reformed gas
US4050904A (en) * 1974-10-07 1977-09-27 Clean Energy Corporation Solubilization and reaction of coal and like carbonaceous feedstocks to hydrocarbons and apparatus therefor
EP0027692A2 (en) * 1979-10-18 1981-04-29 Imperial Chemical Industries Plc A process and reactor for the pyrolysis of a hydrocarbon feedstock
US5551472A (en) * 1994-08-01 1996-09-03 Rpc Waste Management Services, Inc. Pressure reduction system and method
US5620606A (en) * 1994-08-01 1997-04-15 Rpc Waste Management Services, Inc. Method and apparatus for reacting oxidizable matter with particles
US5755974A (en) * 1994-08-01 1998-05-26 Rpc Waste Management Services, Inc. Method and apparatus for reacting oxidizable matter with a salt
US6001243A (en) * 1996-06-07 1999-12-14 Chematur Engineering Ab Heating and reaction system and method using recycle reactor
EP1018366A2 (en) * 1995-05-24 2000-07-12 The Dow Chemical Company Spherical, egg-shaped or oval reactor
US6283626B1 (en) * 1998-10-02 2001-09-04 Institute For Advanced Engineering Multiphase mixing apparatus using acoustic resonance
US6958122B1 (en) 1999-09-03 2005-10-25 Chematur Engineering Ab High pressure and high temperature reaction system
US20080073292A1 (en) * 2004-11-15 2008-03-27 Chematur Engineering Ab Reactor and Method for Supercritical Water Oxidation
US20080264873A1 (en) * 2004-11-15 2008-10-30 Anders Gidner Method and System for Supercritical Water Oxidation of a Stream Containing Oxidizable Material
CN105524642A (en) * 2014-10-21 2016-04-27 中国科学院过程工程研究所 Apparatus and method thereof for directly heating and cracking waste polyolefin by oxy-hydrogen combustion method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3351427A (en) * 1963-11-01 1967-11-07 Cabot Corp Vapor phase process for producing metal oxides
US3498753A (en) * 1966-07-04 1970-03-03 Nippon Zeon Co Apparatus for thermal cracking of hydrocarbon
US3563710A (en) * 1968-02-16 1971-02-16 Monsanto Co Polymerization apparatus

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3351427A (en) * 1963-11-01 1967-11-07 Cabot Corp Vapor phase process for producing metal oxides
US3498753A (en) * 1966-07-04 1970-03-03 Nippon Zeon Co Apparatus for thermal cracking of hydrocarbon
US3563710A (en) * 1968-02-16 1971-02-16 Monsanto Co Polymerization apparatus

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4005986A (en) * 1972-11-06 1977-02-01 Nippon Kokan Kabushiki Kaisha Device for making high temperature reformed gas
US4050904A (en) * 1974-10-07 1977-09-27 Clean Energy Corporation Solubilization and reaction of coal and like carbonaceous feedstocks to hydrocarbons and apparatus therefor
EP0027692A2 (en) * 1979-10-18 1981-04-29 Imperial Chemical Industries Plc A process and reactor for the pyrolysis of a hydrocarbon feedstock
EP0027692A3 (en) * 1979-10-18 1981-11-04 Imperial Chemical Industries Plc A process and reactor for the pyrolysis of a hydrocarbon feedstock
US4349432A (en) * 1979-10-18 1982-09-14 Imperial Chemical Industries Limited Pyrolysis of hydrocarbons
US4461742A (en) * 1979-10-18 1984-07-24 Imperial Chemical Industries Plc Pyrolysis of hydrocarbons
US5551472A (en) * 1994-08-01 1996-09-03 Rpc Waste Management Services, Inc. Pressure reduction system and method
US5620606A (en) * 1994-08-01 1997-04-15 Rpc Waste Management Services, Inc. Method and apparatus for reacting oxidizable matter with particles
US5755974A (en) * 1994-08-01 1998-05-26 Rpc Waste Management Services, Inc. Method and apparatus for reacting oxidizable matter with a salt
US5823220A (en) * 1994-08-01 1998-10-20 Rpc Waste Management Services, Inc. Pressure reduction system and method
KR100415889B1 (en) * 1995-05-24 2004-06-26 다우 글로벌 테크놀로지스 인크. Process for the production of allyl chloride and reactors useful in the process
EP1018366A2 (en) * 1995-05-24 2000-07-12 The Dow Chemical Company Spherical, egg-shaped or oval reactor
EP1018366A3 (en) * 1995-05-24 2000-07-26 The Dow Chemical Company Spherical, egg-shaped or oval reactor
US6017460A (en) * 1996-06-07 2000-01-25 Chematur Engineering Ab Heating and reaction system and method using recycle reactor
US6001243A (en) * 1996-06-07 1999-12-14 Chematur Engineering Ab Heating and reaction system and method using recycle reactor
US6283626B1 (en) * 1998-10-02 2001-09-04 Institute For Advanced Engineering Multiphase mixing apparatus using acoustic resonance
US6958122B1 (en) 1999-09-03 2005-10-25 Chematur Engineering Ab High pressure and high temperature reaction system
US20080073292A1 (en) * 2004-11-15 2008-03-27 Chematur Engineering Ab Reactor and Method for Supercritical Water Oxidation
US20080264873A1 (en) * 2004-11-15 2008-10-30 Anders Gidner Method and System for Supercritical Water Oxidation of a Stream Containing Oxidizable Material
CN105524642A (en) * 2014-10-21 2016-04-27 中国科学院过程工程研究所 Apparatus and method thereof for directly heating and cracking waste polyolefin by oxy-hydrogen combustion method
CN105524642B (en) * 2014-10-21 2017-10-03 中国科学院过程工程研究所 Oxyhydrogen combustion method directly heats the device and method of cracking waste polyolefin

Similar Documents

Publication Publication Date Title
US3849075A (en) Cracking reactor
US3985820A (en) Cracking process
CA1137522A (en) Method of producing olefins from hydrocarbons
US4879104A (en) Process for producing carbon black
US2377245A (en) Process for producing acetylene
US2941021A (en) Process and device for carrying out chemical reactions at high temperatures
US4997525A (en) Hydrocarbon cracking apparatus
US3927185A (en) Process for producing carbon disulfide
US2599981A (en) Carbon black
US2419565A (en) Carbon black process and apparatus
US3959401A (en) Process for cracking
GB825841A (en) Method of carrying out endothermic chemical gas reactions
US4777318A (en) Process and furnace for the steam cracking of hydrocarbons for the preparation of olefins and diolefins
US2989380A (en) Apparatus for carrying out chemical reactions
US3170863A (en) Hydrocarbon conversion process
GB2024847A (en) Cracking hydrocarbons
US5124003A (en) Apparatus for the steam cracking of hydrocarbons for the preparation of olefins an diolefins
US3178488A (en) Production of unsaturates by the nonuniform mixing of paraffin hydrocarbons with hot combustion gases
US3005857A (en) Process for the production of unsaturated hydrocarbons from liquid hydrocarbons
US3098883A (en) Process and apparatus for carrying out chemical reactions at high temperatures
US2548759A (en) Fluid mixer-reactor
US3246957A (en) Apparatus for acetylene production by partial combustion of hydrocarbons
US3254964A (en) Apparatus for the production of acetylene by incomplete combustion of hydrocarbons
US3523758A (en) Apparatus for producing carbon black
US3363024A (en) Hydrogenation of hydrocarbon oils

Legal Events

Date Code Title Description
AS Assignment

Owner name: MORGAN GUARANTY TRUST COMPANY OF NEW YORK, AND MOR

Free format text: MORTGAGE;ASSIGNORS:UNION CARBIDE CORPORATION, A CORP.,;STP CORPORATION, A CORP. OF DE.,;UNION CARBIDE AGRICULTURAL PRODUCTS CO., INC., A CORP. OF PA.,;AND OTHERS;REEL/FRAME:004547/0001

Effective date: 19860106

AS Assignment

Owner name: UNION CARBIDE CORPORATION,

Free format text: RELEASED BY SECURED PARTY;ASSIGNOR:MORGAN BANK (DELAWARE) AS COLLATERAL AGENT;REEL/FRAME:004665/0131

Effective date: 19860925