US3098883A - Process and apparatus for carrying out chemical reactions at high temperatures - Google Patents
Process and apparatus for carrying out chemical reactions at high temperatures Download PDFInfo
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- US3098883A US3098883A US795077A US79507759A US3098883A US 3098883 A US3098883 A US 3098883A US 795077 A US795077 A US 795077A US 79507759 A US79507759 A US 79507759A US 3098883 A US3098883 A US 3098883A
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- 238000000034 method Methods 0.000 title claims description 26
- 238000006243 chemical reaction Methods 0.000 title description 17
- 238000002485 combustion reaction Methods 0.000 claims description 56
- 229930195733 hydrocarbon Natural products 0.000 claims description 28
- 150000002430 hydrocarbons Chemical class 0.000 claims description 28
- 239000000567 combustion gas Substances 0.000 claims description 27
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000004215 Carbon black (E152) Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 11
- 238000000197 pyrolysis Methods 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 5
- 239000007858 starting material Substances 0.000 claims description 5
- 239000007789 gas Substances 0.000 description 53
- 239000000446 fuel Substances 0.000 description 29
- 239000007800 oxidant agent Substances 0.000 description 15
- 238000004519 manufacturing process Methods 0.000 description 10
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 10
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 9
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 9
- 230000001590 oxidative effect Effects 0.000 description 8
- 239000000376 reactant Substances 0.000 description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
- 239000005977 Ethylene Substances 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229910010293 ceramic material Inorganic materials 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 description 3
- 239000004071 soot Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910001868 water Inorganic materials 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- GXDHCNNESPLIKD-UHFFFAOYSA-N 2-methylhexane Natural products CCCCC(C)C GXDHCNNESPLIKD-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 239000002826 coolant Substances 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 238000011017 operating method Methods 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 230000001172 regenerating effect Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 ethylene, propylene Chemical group 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J12/00—Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor
- B01J12/005—Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor carried out at high temperatures, e.g. by pyrolysis
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/2405—Stationary reactors without moving elements inside provoking a turbulent flow of the reactants, such as in cyclones, or having a high Reynolds-number
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
- C07C4/02—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by cracking a single hydrocarbon or a mixture of individually defined hydrocarbons or a normally gaseous hydrocarbon fraction
- C07C4/04—Thermal processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00157—Controlling the temperature by means of a burner
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S585/00—Chemistry of hydrocarbon compounds
- Y10S585/919—Apparatus considerations
- Y10S585/921—Apparatus considerations using recited apparatus structure
- Y10S585/922—Reactor fluid manipulating device
- Y10S585/923—At reactor inlet
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S585/00—Chemistry of hydrocarbon compounds
- Y10S585/949—Miscellaneous considerations
- Y10S585/953—Pulsed, sonic, or plasma process
Definitions
- the present invention relates to a process and to an apparatus for carrying out chemical reactions at high temperatures.
- the energy may be supplied indirectly by passing the gases to be cracked through externally heated pipes or heat exchangers.
- This method involves the disadvantage that the Walls of the pipes become superheated and thus give rise to pronounced formation of coke and soot.
- the method referred to is restricted to the use of small diameter pipes, since a pipe of greater diameter entails too slow and incomplete a heat transfer from the walls to the gas.
- the gases in the border zones become too hot While the gases in the middle zones do not become hot enough and, therefore, do not participate in the reaction.
- regenerative furnaces heated with a gas mixture obtained by combustion of fuel with
- heating is interrupted and the furnace is rinsed out with an inert gas and then charged with the hydrocarbons to be cracked in contact with the hot filling material of the furnaces.
- the furnace is again heated with heating gas.
- This operation is continually repeated by automatic commutation at intervals of a few minutes.
- this process entails the further disadvantages of the inevitable deposition of tarry substances in the regenerative furnace and the constantly changing temperature of the furnace which jeopardize the economy of the process and the yields obtained.
- the energy required for cracking is supplied directly by subjecting part of the hydrocarbon to be cracked to a combustion process in a special combustion device with oxygen, whereby the hydrocarbon itself furnishes the energy for pyrolysis of the hydrocarbon in excess.
- This process is, however, not applicable when it is desired to prevent the hydrocarbon to be cracked from partial combustion.
- a carrier gas for example hydrogen or a combustion gas such as steam heated to a high temperature
- a combustion gas such as steam heated to a high temperature
- heating gas there may also be used all products obtained by combustion of any combustible substance.
- combustion devices supplied with pre-mixed gases involves the risk, however, that the flame may flash back into the mixing chamber and destroy the whole apparatus unless the gas supply lines are provided with very sensitive and in most cases technically complicated control devices to maintain constant pressure and velocity of flow of the mixture of oxygen and vaporized or gaseous fuel, such as hydrogen, as is the case with combustion devices used for the incomplete combustion of methane or natural gas with oxygen. Allthese disadvantages are overcome by the present invention which provides a combustion chamber for performing any pyrolytic reaction.
- the present invention provides a process for the production of acetylene and/or ethylene and/or higher olefinic hydrocarbons having 2-4 carbon atoms by pyrolysis of a hydrocarbon in contact with very hot combustion gases produced in a combustion chamber by the continuous combustion of fuel and'gaseous oxidizing agents.
- the hydrocarbon can be introduced in the form of a gas or vapor either radially or tangentially with the same or opposite direction of rotation of the combustion gases. After a short time of reaction the hot gas mixture is chilled.
- the combustion gases are produced by introducing the fuel and a deficiency of oxidizing gas separately into the combustion chamber, for example at a velocity correspond ing to a Mach-number of at least 0.8, for instance at sonic speed, Where they are subjected to a combustion process.
- combustion .process can "be also carried out in a manner such that the wall of thecombustion chamber is largely separated from the combustion gas by a layer of the fuel or the oxidizing agent.
- the fuel and the oxidizing agents are mixed so completely that a very short flame is produced.
- fuel and oxidizing agents undergo so rapid a combustion that the resulting flarne ceases to burn after a very short distance.
- the combustion chamber as used in the process of this invention involves the particular advantage that the whole combustion process is performed within the smallest space.as is the case with flames produced with pre-mixed gases-so that the heat losses caused by dissipation are small in relation to the energy produced. Contrary to the known devices, a combustion chamber as used herein prevents the flame from flashing back into the mixing chamber and requires no complicated control mechanism.
- Mach-number is used herein to indicate the ratio bet-ween the gas velocity applied and the sonic speed at the corresponding temperature.
- the operating procedure according to this invention involves the further advantage that the combustion gases leaving the combustion chamber at [flame temperature possess such a high turbulence-due to their having been swirled in said chamber -that they are practically instantaneously mixed with the reactant that is to undergo pyrolysis.
- the heat is particularly well transferred from the combustion gas to the react-ants (hydrocarbons), whereby it is possible to perform a practically complete reaction.
- The'hydrocar-bons to undergo pyrolysis can he intro pokerd into the combustion chamber radially or tangem tially either in one or both directions of rotation. Furthermore, it may be advantageous to' force the combust-ion gases, prior-to their lbei'ng' mixed with the reactant,
- a constricted opening for example a nozzle
- a ring or circle of bore holes means a group of inlets which are arranged in a plane, for ex:
- the desired effect can be further improved by additionally providing the upper part of the burner withone or more bore holes, for. example in the direction of the axis of the burner, as shown in FIGURE 2; Inlet 111 is in the center of the upper part of the burner. advantage to introduce fuel through that inlet when oxidizing agent is supplied through the upper circle of bore holes and vice versa.
- the complete angular momentum of the combustion gases produced can be largely varied or even wholly suppressed.
- the bore holes have a tangential direction; it is preferred, however, to arrange the bore holes in a manner such that the projection of the axis of the bore holes of one circle, preferably the inlets for the fuel, forms clockwise an angle of less than with the projection of the appertaining tangent to the inner wall of the burner.
- a ring of bore holes in which the projection of the axis of the bore holes forms clockwise an angle of more than 90 with the projection of the appertaining tangent to the inner wall of the burner.
- the projections are referred to a plane in vertical position to the axis of the burner. Tangential inlets are especially prefer-red.
- the position and direction of their inlets may further regulate the angular It has proved advantageous to provide the burner with inlets for the secondary gas where the gasesistrearning on the wall and supplied through the circle of inlets being next to the lburner outlet have just burned. Thus the wall of the burner is effectively cooled and the secondary gases do not impair the combustion. It is furthermore advisable to arrange the inlets for the secondary gas in a direction such that an angular momentum is imparted to the secondary gas, the direction of which corresponds to that of the medium streaming off the next higher ring of nozzles.
- inlet rings of different diameters on various bodies, for example on a top of a burner having the form of a cone-shaped shell (FIGURE 3) or a dome-shaped shell (FIGURE 4) it proved to he particularly advantageous to use a burner the upper part of which is composed of concentric cylinder jackets provided with bore holes and of interconnecting circular ring disks (FIGURES l and 2').
- This arrangement presents the additional advantage that the inlets can be disposed in the combustion chamber at positions where the mixing ratio of the two participants in the combustion process is still below the ignition limit. Thus the combustion and the thermal stress of the Wall near the inlets is avoided.
- the last mentioned arrangement furthermore serves best to the second purpose of the. invention, namely to separate the wall of the burner by fresh gas from the hot combustion gases.
- olefin-containing gases i.e. gases which in addition to acetylene and/or ethylene contain propylene, n-butylene, iso-butylene, etc., that is chiefly olefins with 3 or 4 carbon atoms
- a secondary gas preferably steam and/or hydrogen
- the secondary gas shall suitably have a temperature of at least 150 C. and below the temperature of the combustion gas.
- the addition of said secondary gas reduces the proportion of oxygen-containing radicals, oxygen atoms and oxygen molecules in the combustion gas.
- the secondary gas can be introduced into the combustion gas radially or tangentially and in one or both directions of rotation.
- the secondary gas may likewise be introduced axially, that is to say through the cover of the burner or the outer circular ring disk, for example via bore holes or a ring slot.
- a layer of secondary gas for example steam, is formed between the wall of the burner and the center of the flame so that a separation of carbon is impossible and the dissipation of heat is considerably reduced.
- the hydrocarbon shall be introduced in amounts such that with a reaction time of l0- seconds a temperature of 700 C. is attained at the end of the reaction.
- a reaction time of l0- seconds a temperature of 700 C. is attained at the end of the reaction.
- olefins, especially ethylene are to be produced, it is advantageous to operate with a reaction time of 10 l0* seconds and when acetylene is to be produced it is advisable to add an amount of hydrocarbons such that the temperature of the reaction mixture at the end of the reaction amounts to 1000 C.
- reaction time 10 l0
- aliphatic hydrocarbons which may have been pre-heated are introduced in liquid or gaseous formwhich term is intended to include the vapourized state-either radially or tangentially or in any other known manner into the current of combustion gases so that they are mixed with the latter gases rapidly and completely, and the reacted mixture is chilled in known manner after a short time of reaction, for example by injection of water.
- the reaction chamber for example the reaction tube
- ceramic material to suppress undesirable soot formation which is favoured by metal surfaces.
- a metal which is cooled by means of a cooling agent for example water; however, there may also be used ceramic material or metal lined with ceramic material.
- a cooling agent for example water
- ceramic material or metal lined with ceramic material there may also be used.
- the heat taken up by the cooling agent can be recovered and used for other purposes.
- saturated or unsaturated hydrocarbons con taining up to 30 or more carbon atoms.
- saturated hydrocarbons such as methane, ethane, propane, butane, pentane, heptane, octane, decane, dodecane, especially in the form of liquid commercial mixtures, such as petroleum distillates or hydrocatrbon oils, for example topped Kuwait oil, or also in the form of technical gases such as natural gas.
- aliphatic saturated hydrocarbons containing from 1 to about 30 or more carbon atoms there may also be used unsaturated hydrocarbons and hydrocarbons having a branched chain.
- branched hydrocarbons there are concerned, for example isobutane, isooctane, isoheptane, isohexane, etc. It is not advisable to use unsaturated hydrocarbons unless it is desired to produce acetylene or unless they are contained in small amounts in other hydrocarbons. Thus, for example, ethylene, propylene, nor isobutylene may be used for the production of acetylene.
- fuels suitable for use in the production of acetylene and/ or ethylene and/or higher hydrocarbons there may be used any gaseous or other hydrocarbons that are liquid or can be liquefied by heating. Such fuels are used in a finely divided form for operating the combustion chamber according to this invention and for the production of the aforesaid unsaturated hydrocarbons.
- the term finely divided form as used herein is intended to comprise fine atomization of liquid hydrocarbons and also the gaseous and vapour states.
- oxidizing agent there may advantageously be used commercial pure oxygen, if desired in admixture with air, the oxidizing agent being always employed in a theoreti cally insuflicient quantity.
- EXAMPLE 1 The table illustrates an example to be understood with the aid of FIGURES l and 2. Only relative values are given and the production of angular momenta in the burner is chosen so that their sum disappears.
- the active radius (R in column E represents the radius of the circle round the axis of the burner to which the projection of the appertaining axis of the bore holes forms the tangent.
- the improvement which comprises introducing into the combust-ionzonean excess oflatomized fuel and an oxidizing gas therefor separately and with an oppositely directed angular momenturn at a different distance from theaxis of said combustion zone to form rotating coaxially arranged-hollow atmospheres of different diameter which contrarotate in one another.
- the improvement which comprises introducing into the. combustion zone an excess of atomized. fuel and.
- an oxidizing gas therefor separately through at least two sets of nozzles arranged in annular manner, said annular sets of nozzles being at difierent .distanccs'from the axis vof, said combustion zone and one set of nozzles for thefuel being adjacent and having an angular direction opposite to a set of l s forthe o zi gas, whereby otatin q x ly arranged hollow atmospheres of different diameter are formed which contrarotate in one another.
- streaming direction forms an angle of less than with the projection of the appertaining tangent to the outer limitation of the combustion zone, the projection being referred to a plane perpendicular to the axis of the cornbustion zone.
- An apparatus suitable for the manufacture of unsaturated hydnocarbons consisting of a unitary combustion chamber having a wall provided with at least three annular sets ofnozzles for fuel and oxidizing gas, the annulus in which the nozzles for the fuel are arranged having a diameter difierent from that of the annulus in which nozzles forthe oxidizing gas are arranged and a set of nozzles for the fuel being adjacent and having an angular direction opposite to a setof nozzles for the oxidizing gas so that rotating axially arranged hollow atmospheres of different diametenare formed which .contrarotate in one another and contact each other along their interface.
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- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- General Chemical & Material Sciences (AREA)
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Description
July 23, 1963 Filed Feb. 24, 1959 EUSE ET AL 3,098,883
0. H PROCESS AND APPARATUS FOR CARRYING OUT CHEMICAL REACTIONS AT HIGH TEMPERATURES 2 Sheets-Sheet l BY m,mv%4
ArrO/PA/EVJ.
y 1963 o. HEUSE ETAL 3,098,883
PROCESS AND APPARATUS FOR CARRYING our CHEMICAL 2 Sheets-Sheet 2 REACTIONS AT HIGH TEMPERATURES' Filed Feb. 24, 1959 FRIEDRICH HOP/V HTTO/P/VEKSZ United States Patent 6 3,098,883 PROCESS AND APPARATUS FOR CARRYING OUT CHEMICAL REACTIONS AT HIGH TEMPERATURES Otto Heuse, Kronberg, Taunus, Werner Fischer, Bad Soden, Taunus, and Friedrich Horn and Rudolf Wimmer, Frankfurt am Main, Germany, assignors to Farbwerke Hoechst Aktiengesellschaft vormals Meister Lucius 8: Briining, Frankfurt am Main, Germany, a corporation of Germany Filed Feb. 24, 1959, Ser. No. 795,077 Claims priority, application Germany Feb. 28, 1%8
' 13 Claims. (Cl. 260-683) The present invention relates to a process and to an apparatus for carrying out chemical reactions at high temperatures.
It is known that the production of acetylene, ethylene and higher o-lefines from methane, ethane or higher hydrocarbons requires the supply within the shortest possible time to the hydrocarbons to be reacted of large amounts of energy.
Thus, for example, the energy may be supplied indirectly by passing the gases to be cracked through externally heated pipes or heat exchangers. This method involves the disadvantage that the Walls of the pipes become superheated and thus give rise to pronounced formation of coke and soot. Furthermore, the method referred to is restricted to the use of small diameter pipes, since a pipe of greater diameter entails too slow and incomplete a heat transfer from the walls to the gas. The gases in the border zones become too hot While the gases in the middle zones do not become hot enough and, therefore, do not participate in the reaction.
For the indirect supply of heat there are also used socalled regenerative furnaces heated with a gas mixture obtained by combustion of fuel with When the furnace is hot, heating is interrupted and the furnace is rinsed out with an inert gas and then charged with the hydrocarbons to be cracked in contact with the hot filling material of the furnaces. After a minimum temperature has been reached, the furnace is again heated with heating gas. This operation is continually repeated by automatic commutation at intervals of a few minutes. In addition to the necessary complicated automatic reversing device, this process entails the further disadvantages of the inevitable deposition of tarry substances in the regenerative furnace and the constantly changing temperature of the furnace which jeopardize the economy of the process and the yields obtained.
According to another process the energy required for cracking is supplied directly by subjecting part of the hydrocarbon to be cracked to a combustion process in a special combustion device with oxygen, whereby the hydrocarbon itself furnishes the energy for pyrolysis of the hydrocarbon in excess. This process is, however, not applicable when it is desired to prevent the hydrocarbon to be cracked from partial combustion.
Therefore, it has repeatedly been proposed to supply the energy by means of a carrier gas, for example hydrogen or a combustion gas such as steam heated to a high temperature, which is then mixed in a suitable manner with the hydrocarbons to be cracked. In this case, it is especially advantageous to use as fuel hydrogen and to subject this substance together with oxygen to a com- 3',098883' Patented July 23, 1963 bustion process since, after the reaction, the steam formed can be easily separated from the resulting gas by condensation and since the subsequent separation of the gas is thereby rendered less difiicult. As heating gas there may also be used all products obtained by combustion of any combustible substance. Furthermore, it is particularly advantageous to perform the combustion of the fuel within a fairly small space and to provide for as short a distance as possible between the end of the combustion zone and the hydrocarbon to be cracked, so that the inevitable heat losses caused by dissipation are kept as small as possible. Accordingly a fairly short flame is required which furnishes large amounts of energy but burns only for a short distance. To this end, the combustion gas and the oxidizing agent are often pre-mixed in a separate mixing chamber before they are introduced into the combustion chamber, proper. The use of combustion devices supplied with pre-mixed gases involves the risk, however, that the flame may flash back into the mixing chamber and destroy the whole apparatus unless the gas supply lines are provided with very sensitive and in most cases technically complicated control devices to maintain constant pressure and velocity of flow of the mixture of oxygen and vaporized or gaseous fuel, such as hydrogen, as is the case with combustion devices used for the incomplete combustion of methane or natural gas with oxygen. Allthese disadvantages are overcome by the present invention which provides a combustion chamber for performing any pyrolytic reaction. More particularly, the present invention provides a process for the production of acetylene and/or ethylene and/or higher olefinic hydrocarbons having 2-4 carbon atoms by pyrolysis of a hydrocarbon in contact with very hot combustion gases produced in a combustion chamber by the continuous combustion of fuel and'gaseous oxidizing agents. The hydrocarbon can be introduced in the form of a gas or vapor either radially or tangentially with the same or opposite direction of rotation of the combustion gases. After a short time of reaction the hot gas mixture is chilled. The combustion gases are produced by introducing the fuel and a deficiency of oxidizing gas separately into the combustion chamber, for example at a velocity correspond ing to a Mach-number of at least 0.8, for instance at sonic speed, Where they are subjected to a combustion process.
It may likewise be possible to introduce the gases at a lower velocity than corresponds to a Mach-number of 0.8. In some cases it is suitable to carry out said reaction with a small angular momentum or even in a manner such that the reactants do not possess any angular momentum at all. This fact sometimes involves the advantage that the low degree of formation of soot or carbon particles on the wall of the reaction chamber, which may occur when especially high boiling oils are used as starting materials, can be still further reduced. The combustion .process can "be also carried out in a manner such that the wall of thecombustion chamber is largely separated from the combustion gas by a layer of the fuel or the oxidizing agent.
These results can be achieved by introducing the fuel and the oxidizing agent in several planes through several bore holes into the upper part of the burner which is opposite to the mouth of the burner, the walls of the said upper part "being formed in a manner such that the bore holes are at different distances from the center of the burner as shown, for example, in FIGURE 1 of the accompanying drawings. Thus the fuel and the oxidizing agent form in the burner contrarotating atmospheres of coaxial hollow spaces of different diameters.
The fuel and the oxidizing agents are mixed so completely that a very short flame is produced. By mixing and swirling as described above fuel and oxidizing agents undergo so rapid a combustion that the resulting flarne ceases to burn after a very short distance.
It is, therefore, possible to operate the combustion chamber with very high loads. industrially, itis especially advantageous to operate the combustion chamber with evolution of heat at the rate of 1 billion or vmore Kcal./m. h. (l Kcal.). The combustion chamber as used in the process of this invention involves the particular advantage that the whole combustion process is performed within the smallest space.as is the case with flames produced with pre-mixed gases-so that the heat losses caused by dissipation are small in relation to the energy produced. Contrary to the known devices, a combustion chamber as used herein prevents the flame from flashing back into the mixing chamber and requires no complicated control mechanism.
The term Mach-number 'is used herein to indicate the ratio bet-ween the gas velocity applied and the sonic speed at the corresponding temperature.
The operating procedure according to this invention involves the further advantage that the combustion gases leaving the combustion chamber at [flame temperature possess such a high turbulence-due to their having been swirled in said chamber -that they are practically instantaneously mixed with the reactant that is to undergo pyrolysis. Thus, the heat is particularly well transferred from the combustion gas to the react-ants (hydrocarbons), whereby it is possible to perform a practically complete reaction.
The'hydrocar-bons to undergo pyrolysis can he intro duced into the combustion chamber radially or tangem tially either in one or both directions of rotation. Furthermore, it may be advantageous to' force the combust-ion gases, prior-to their lbei'ng' mixed with the reactant,
through a constricted opening, for example a nozzle, in
order to increase their axial velocity.
In the following a ring or circle of bore holes means a group of inlets which are arranged in a plane, for ex:
ample, in a position perpendicular to the axis of the burner. In the extreme case a ring of bore holes only contains one inlet. All bore holes hientioned in the presentspeciflcation serve to supply the burner either with the oxidizing agent or with the fuel, which may he a "gas mixture. Onering of bore holes may likewise he provided with inlets for the different reactants.
For carrying out the process according to the present invention a device may be used as shown diagrammatically in the accompanying drawings.
It is of advantage to introduce into the upper part of a burner 10 through one ring or circle of bore holes 2 (of. FIGURES l and 2) the fuel in one direction of angular momentum and through the following ring of inlets 3 the oxidizing agent in oppositedirection of angular momentum. By this means the fuel and the oxidizing agent form in the burner atmospheres having approximately the shape of concentric hollow cylinders (annuli) which contrarotate in one another .and which mix thoroughly at the border surfaces due to the high relative velocity formed.
The desired effect can be further improved by additionally providing the upper part of the burner withone or more bore holes, for. example in the direction of the axis of the burner, as shown in FIGURE 2; Inlet 111 is in the center of the upper part of the burner. advantage to introduce fuel through that inlet when oxidizing agent is supplied through the upper circle of bore holes and vice versa.
It is of.
'momentum ofthe gases in the. lburner.
By suitably selecting the amounts of fuel and oxidizing agent supplied through the individual inlets, the inlet velocity into the burner, the direction of the bore holes and finally the diameter of the circle of nozzles the complete angular momentum of the combustion gases produced can be largely varied or even wholly suppressed. Furthermore it is not necessary that the bore holes have a tangential direction; it is preferred, however, to arrange the bore holes in a manner such that the projection of the axis of the bore holes of one circle, preferably the inlets for the fuel, forms clockwise an angle of less than with the projection of the appertaining tangent to the inner wall of the burner. Contiguous to said circle of bore holes there is suitably arranged a ring of bore holes in which the projection of the axis of the bore holes forms clockwise an angle of more than 90 with the projection of the appertaining tangent to the inner wall of the burner. The projections are referred to a plane in vertical position to the axis of the burner. Tangential inlets are especially prefer-red.
In case further gases, such as secondary gases, are supplied in addition to the fuel and the oxidizing agent, for example through inlets 4a and 4b, the amount and nature of the secondary gases used, the position and direction of their inlets may further regulate the angular It has proved advantageous to provide the burner with inlets for the secondary gas where the gasesistrearning on the wall and supplied through the circle of inlets being next to the lburner outlet have just burned. Thus the wall of the burner is effectively cooled and the secondary gases do not impair the combustion. It is furthermore advisable to arrange the inlets for the secondary gas in a direction such that an angular momentum is imparted to the secondary gas, the direction of which corresponds to that of the medium streaming off the next higher ring of nozzles.
In general lburners of the type described above are shaped in axially symrnctricmanner round the axis which is vertical according to'the drawings. I-t is likewise possible, however, to use other variants which are elliptic or polygonal. In this case the terms used in the present specification which are taken from theno menclature of the rotation symmetry, such as circle or cylinder, are to be replaced by analogous terms.
Although it is possible to arrange inlet rings of different diameters on various bodies, for example on a top of a burner having the form of a cone-shaped shell (FIGURE 3) or a dome-shaped shell (FIGURE 4) it proved to he particularly advantageous to use a burner the upper part of which is composed of concentric cylinder jackets provided with bore holes and of interconnecting circular ring disks (FIGURES l and 2'). This arrangement presents the additional advantage that the inlets can be disposed in the combustion chamber at positions where the mixing ratio of the two participants in the combustion process is still below the ignition limit. Thus the combustion and the thermal stress of the Wall near the inlets is avoided. The last mentioned arrangement furthermore serves best to the second purpose of the. invention, namely to separate the wall of the burner by fresh gas from the hot combustion gases.
The same advantage present, for example, an upper part of the burner as shown in [FIGURE 5, which is composed of cone-shaped shells having different inclinations in which a cone-shaped shell of greater inclination carrying a circle of bore holes is followed by a cone-shaped shell of inferior inclination which is free from bore holes and other variants thereof. Although the purpose of the present invention can be achieved by very different combinations of the above features the best results are obtained when the axes of the bore holes of one ring are arrangedin general in one plane. For reasons of production an inclination of the axes of the bore holes may likewise be advisable (cf. FIGURE -5). In order to produce optimum conditions of flow it is particularly desirable to arrange the axes of the major part of the inlets or of all inlets of a circle so that their projection on a plane in vertical position to the axis of the burner does not cut the projection of the next higher circle of bore holes and to install between the combustion chamber and the point of introduction of the reactant a constriction, for example in the form of a nozzle.
When it is desired to manufacture acetylene and/or ethylene and/or higher olefin-containing gases, i.e. gases which in addition to acetylene and/or ethylene contain propylene, n-butylene, iso-butylene, etc., that is chiefly olefins with 3 or 4 carbon atoms, it is especially suitable to admix, between the flame end and the place where the reactant is introduced, a secondary gas, preferably steam and/or hydrogen.
The secondary gas shall suitably have a temperature of at least 150 C. and below the temperature of the combustion gas. The addition of said secondary gas reduces the proportion of oxygen-containing radicals, oxygen atoms and oxygen molecules in the combustion gas. By this means it is furthermore possible to influence the angular momentum of the combustion gases or to compensate completely the residual angular momentum thereof.
This operating procedure is especially suitable if fuels are used that produce flames and combustion gases, such as have very high temperatures, for example hydrogen. In this case, the secondary gas can be introduced into the combustion gas radially or tangentially and in one or both directions of rotation.
The secondary gas may likewise be introduced axially, that is to say through the cover of the burner or the outer circular ring disk, for example via bore holes or a ring slot. By this latter step a layer of secondary gas, for example steam, is formed between the wall of the burner and the center of the flame so that a separation of carbon is impossible and the dissipation of heat is considerably reduced. It is especially advantageous to use as secondary gas hydrogen and/or steam in an amount of 1-80 parts by weight, preferably 30-70 parts by weight, calculated on the total amount of the combustion gases.
In the pyrolysis the hydrocarbon shall be introduced in amounts such that with a reaction time of l0- seconds a temperature of 700 C. is attained at the end of the reaction. When olefins, especially ethylene, are to be produced, it is advantageous to operate with a reaction time of 10 l0* seconds and when acetylene is to be produced it is advisable to add an amount of hydrocarbons such that the temperature of the reaction mixture at the end of the reaction amounts to 1000 C. In this case it is expedient to operate with a reaction time of 10 l0 For the production of acetylene and/ or ethylene and/ or other olefines containing 2 to 4 carbon atoms, for example propylene or butylene using a combustion device according to this invention, aliphatic hydrocarbons which may have been pre-heated are introduced in liquid or gaseous formwhich term is intended to include the vapourized state-either radially or tangentially or in any other known manner into the current of combustion gases so that they are mixed with the latter gases rapidly and completely, and the reacted mixture is chilled in known manner after a short time of reaction, for example by injection of water. In this case it is especially advantageous to line the reaction chamber, for example the reaction tube, with ceramic material to suppress undesirable soot formation which is favoured by metal surfaces.
For the construction of the combustion chamber it is expedient to use a metal which is cooled by means of a cooling agent, for example water; however, there may also be used ceramic material or metal lined with ceramic material. In the case of a cooled metal combustion chamber, the heat taken up by the cooling agent can be recovered and used for other purposes.
As starting materials suitable for use in the process of this invention there can be used the known hydrocarbons,
for example saturated or unsaturated hydrocarbons con taining up to 30 or more carbon atoms. It is particularly advantageous to employ saturated hydrocarbons, such as methane, ethane, propane, butane, pentane, heptane, octane, decane, dodecane, especially in the form of liquid commercial mixtures, such as petroleum distillates or hydrocatrbon oils, for example topped Kuwait oil, or also in the form of technical gases such as natural gas. Instead of aliphatic saturated hydrocarbons containing from 1 to about 30 or more carbon atoms there may also be used unsaturated hydrocarbons and hydrocarbons having a branched chain. As branched hydrocarbons there are concerned, for example isobutane, isooctane, isoheptane, isohexane, etc. It is not advisable to use unsaturated hydrocarbons unless it is desired to produce acetylene or unless they are contained in small amounts in other hydrocarbons. Thus, for example, ethylene, propylene, nor isobutylene may be used for the production of acetylene.
As fuels suitable for use in the production of acetylene and/ or ethylene and/or higher hydrocarbons there may be used any gaseous or other hydrocarbons that are liquid or can be liquefied by heating. Such fuels are used in a finely divided form for operating the combustion chamber according to this invention and for the production of the aforesaid unsaturated hydrocarbons. The term finely divided form as used herein is intended to comprise fine atomization of liquid hydrocarbons and also the gaseous and vapour states. As fuels there may also be used hydrogen, carbon monoxide or Water gas which contains an excess of hydrogen and/ or carbon monoxide.
As oxidizing agent there may advantageously be used commercial pure oxygen, if desired in admixture with air, the oxidizing agent being always employed in a theoreti cally insuflicient quantity.
The following examples illustrate the invention, but they are not intended to limit it thereto.
EXAMPLE 1 The table illustrates an example to be understood with the aid of FIGURES l and 2. Only relative values are given and the production of angular momenta in the burner is chosen so that their sum disappears. The active radius (R in column E represents the radius of the circle round the axis of the burner to which the projection of the appertaining axis of the bore holes forms the tangent.
R is in relation with the radius R of the ring of bore holes and the angle to formed by the projection of the axis of the inlets with the projection of the appertaining tangent to the circle of nozzles: R,=R-cos go.
' In the following table In stands for mass, 1 for length and t for time.
Table A B C D E F G Produc- Activc tion of Direc- Flow radius Inlet angular tion of (Rt) velocity momen- Inlet Medium angular t momen- G=DEF turn m -t- Z Z-tm .12 .t-z
7 0 300 0 2 15 250 7500 7 30 300 +6300() 7 30 300 +63000 2 45 250 22500 2 45 250 22500 Sec.-gas 5 45 163 36750 Sec.-gas- 5 45 163 36750 EXAMPLE 2 6 kilograms of light gasoline, 2 m. of hydrogen (measured lat N.T.P.) and 15.8 m of oxygen (at N.T.P.) are burned per hour in a combustion chamber into which the components which are liquid at room temperature there are obtained per hour 40.6 m? (at N.T.P.) of a gas mixture composed (in percent by volume) of N +o 1.3 CO2 14.5 C 14.8 H2 25.6 CH 11.6 C H 8.0 C H 18.7 C H 1.3 The residue contains various higher hydrocanbons.
Weclaim;
1. In a process for the pyrolysis of aliphatichydrocan bons by continuously.formingastream of hot combustion. gas in a combustion zone, contacting said combustion gas fora short time with, an atomized aliphatic hydrocarbon for pyrolysis thereofto yield C2- to C -unsaturatedhydrocarbons having less hydrogen in the molecule than the starting material, and chilling the effluent mixture of pyro: lyzed. hydnocarbonand combustion gas, the improvement which comprises introducing into the combust-ionzonean excess oflatomized fuel and an oxidizing gas therefor separately and with an oppositely directed angular momenturn at a different distance from theaxis of said combustion zone to form rotating coaxially arranged-hollow atmospheres of different diameter which contrarotate in one another.
2. In a process for the pyrolysis of aliphatic hydrocarbons by continuously forminga stream of hot combustion gas in a combustion zone, contacting said combustion.
gas for a shorttime with an atomized aliphatichydrm carbon for pyrolysis thereof to yield C toC -unsaturated hydrocarbons having less hydrogen in the molecule than. the starting material, and chillingthe effluent mixture of pyrolyzed hydrocarbon and combustion gas, the improvement which comprises introducing into the. combustion zone an excess of atomized. fuel and. an oxidizing gas therefor separately through at least two sets of nozzles arranged in annular manner, said annular sets of nozzles being at difierent .distanccs'from the axis vof, said combustion zone and one set of nozzles for thefuel being adjacent and having an angular direction opposite to a set of l s forthe o zi gas, whereby otatin q x ly arranged hollow atmospheres of different diameter are formed which contrarotate in one another.
3. A process as claimed in claim 1, wherein the fuel and the oxidizing gas are introduced into the combustion zone in a manner such as to yield a total angular momentum of the gases in the combustion zone which is substantially about nil.
4. A process as claimed inclaim 1, wherein the fuel and the oxidizing gas are introduced into the combustion zone in such a manner that the projection of. theaxis of .the
streaming direction forms an angle of less than with the projection of the appertaining tangent to the outer limitation of the combustion zone, the projection being referred to a plane perpendicular to the axis of the cornbustion zone.
5. A process as claimed in claim 1, wherein at least one of the reactants of the combustion reaction is tangentially introduced into the combustion zone.
6. A process as claimed in claim 1, wherein a secondary gas is admixed to the combustion gases.
7. A process as claimed'in claim 6, wherein the secondary gas is introduced into the combustion zone in such a direction that it is given an angular momentum in the combustion zone in the same direction as has the medium which is introduced through the adjacent nozzles.
8, A process as claimed in claim 1, wherein the velocity of the combustion gases is. increased when. leaving the combustion zone but before. the hydrocarbon to be pyrolyzed is introduced.
9. An apparatus suitable for the manufacture of unsaturated hydnocarbons consisting of a unitary combustion chamber having a wall provided with at least three annular sets ofnozzles for fuel and oxidizing gas, the annulus in which the nozzles for the fuel are arranged having a diameter difierent from that of the annulus in which nozzles forthe oxidizing gas are arranged and a set of nozzles for the fuel being adjacent and having an angular direction opposite to a setof nozzles for the oxidizing gas so that rotating axially arranged hollow atmospheres of different diametenare formed which .contrarotate in one another and contact each other along their interface.
10. An apparatusas defined in claim 9 wherein the pnojections, ofthe axes of the nozzles of one set of nozzles donotintersect theprojection .of the wall which contains thenozzlesof an, a djacent set, referred to a plane perpendicular to the axis of the combustion chamber.
11. An. apparatus asclaimed in claim 9, wherein sets ofnpzzles are adjacent with each other in which the projectionsof the axes ,of the nozzles of one set with the projection of .the. appertaining tangent to the inner wall of .the.combustio n chamber form clockwise a smaller angle than 90"; while theprojections of the axes of an adjacent set of nozzleswith the appertaining tangent to the inner wallof the combustionchamber forms clockwise an angle of. more. than 90.
12. An. apparatus as claimed in. claim 9, wherein the upperpart of thecombustion chamber is composed of concentric cylindrical jackets provided with bore holes and of interconnecting circular ring disks.
13; A modificationofthe apparatus claimed in claim 9, wherein the upper part ofthe combustion chamber is addition-ally provided with at least one nozzle forat least one of the reactants-which is arranged in an axial direction.
References Cited in the file of this patent UNITED STATES PATENTS 2,162,433" Hillhouse June 13, 1939 2,353,509 Schultze July 11, 1944 2,375,795 Krejci May 15, 1945 2,413,407 Dreyfus Dec. 31, 1946 2,813,138 M'acQueen Nov. 12, 1957
Claims (1)
1. IN A PROCESS FOR THE PYROLYSIS OF ALIPHATIC HYDROCARBONS BY CONTINUOUSLY FORMING A STREAM OF HOT COMBUSTION GAS IN A COMBUSTION ZONE, CONTACTING SAID COMBUSTION GAS FOR A SHORT TIME WITH AN ATOMIZED ALIPHATIC HYDROCARBON FOR PYROLYSIS THEREOF TO YIELD C2- TO C4-UNSATURATED HYDROCARBONS HAVING LESS HYDROGEN IN THE MOLECULE THAN THE STARTING MATERIAL, AND CHILLING THE EFFLUENT MIXTURE OF PYROLYZED HYDROCARBON AND COMBUSTION GAS, THE IMPROVEMENT WHICH COMPRISES INTRODUCING INTO THE COMBUSTION ZONE AN
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3098883X | 1958-02-28 |
Publications (1)
| Publication Number | Publication Date |
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| US3098883A true US3098883A (en) | 1963-07-23 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US795077A Expired - Lifetime US3098883A (en) | 1958-02-28 | 1959-02-24 | Process and apparatus for carrying out chemical reactions at high temperatures |
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| US (1) | US3098883A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3885919A (en) * | 1972-11-24 | 1975-05-27 | Marcel T Pillard | Residual gas burner with superimposed, increasing size burning chambers |
| US3959401A (en) * | 1973-05-14 | 1976-05-25 | Union Carbide Corporation | Process for cracking |
| US4134966A (en) * | 1976-06-29 | 1979-01-16 | Phillips Petroleum Company | Carbon black process with inner and outer hot combustion gas entries providing protective blanket and extra hot gases for conversion of feed |
| US4321248A (en) * | 1980-04-30 | 1982-03-23 | Phillips Petroleum Company | Method for vortex flow carbon black production |
| WO1996029143A1 (en) * | 1995-03-20 | 1996-09-26 | Schmidt, Hermann | Fluid compound thermochemical conversion process and converter |
| US20100099052A1 (en) * | 2002-08-09 | 2010-04-22 | Jfe Steel Corporation | Tubular flame burner and combustion control method |
| US10570345B2 (en) * | 2011-11-08 | 2020-02-25 | Exxonmobil Chemical Patents Inc. | Regenerative reactor system |
| EP3976571A4 (en) * | 2019-05-27 | 2023-06-14 | Council Of Scientific & Industrial Research | An intensified process of synthesis of dialkyl ethers using a step conical reactor |
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| US2162433A (en) * | 1936-01-27 | 1939-06-13 | Sylvia Remsen Hillhouse | Method for producing gasoline |
| US2353509A (en) * | 1942-02-06 | 1944-07-11 | Phillips Petroleum Co | Process for hydrocarbon conversion |
| US2375795A (en) * | 1941-12-22 | 1945-05-15 | Phillips Petroleum Co | Carbon black process |
| US2413407A (en) * | 1941-12-18 | 1946-12-31 | Bonard Claude | Method of cracking hydrocarbons in the presence of a diluent gas |
| US2813138A (en) * | 1953-07-27 | 1957-11-12 | Phillips Petroleum Co | Production of unsaturated hydrocarbons and reactor therefor |
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| US2162433A (en) * | 1936-01-27 | 1939-06-13 | Sylvia Remsen Hillhouse | Method for producing gasoline |
| US2413407A (en) * | 1941-12-18 | 1946-12-31 | Bonard Claude | Method of cracking hydrocarbons in the presence of a diluent gas |
| US2375795A (en) * | 1941-12-22 | 1945-05-15 | Phillips Petroleum Co | Carbon black process |
| US2353509A (en) * | 1942-02-06 | 1944-07-11 | Phillips Petroleum Co | Process for hydrocarbon conversion |
| US2813138A (en) * | 1953-07-27 | 1957-11-12 | Phillips Petroleum Co | Production of unsaturated hydrocarbons and reactor therefor |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3885919A (en) * | 1972-11-24 | 1975-05-27 | Marcel T Pillard | Residual gas burner with superimposed, increasing size burning chambers |
| US3959401A (en) * | 1973-05-14 | 1976-05-25 | Union Carbide Corporation | Process for cracking |
| US4134966A (en) * | 1976-06-29 | 1979-01-16 | Phillips Petroleum Company | Carbon black process with inner and outer hot combustion gas entries providing protective blanket and extra hot gases for conversion of feed |
| US4321248A (en) * | 1980-04-30 | 1982-03-23 | Phillips Petroleum Company | Method for vortex flow carbon black production |
| WO1996029143A1 (en) * | 1995-03-20 | 1996-09-26 | Schmidt, Hermann | Fluid compound thermochemical conversion process and converter |
| US6555727B2 (en) | 1995-03-20 | 2003-04-29 | Michael L. Zettner | Fluid compound thermochemical conversion process and converter |
| US20100099052A1 (en) * | 2002-08-09 | 2010-04-22 | Jfe Steel Corporation | Tubular flame burner and combustion control method |
| US20100104991A1 (en) * | 2002-08-09 | 2010-04-29 | Jfe Steel Corporation | Tubular flame burner |
| US8944809B2 (en) * | 2002-08-09 | 2015-02-03 | Jfe Steel Corporation | Tubular flame burner and combustion control method |
| EP1528316B1 (en) * | 2002-08-09 | 2017-10-04 | JFE Steel Corporation | Combustion controller for tubular flame burner and method for controlling combustion |
| US10570345B2 (en) * | 2011-11-08 | 2020-02-25 | Exxonmobil Chemical Patents Inc. | Regenerative reactor system |
| EP3976571A4 (en) * | 2019-05-27 | 2023-06-14 | Council Of Scientific & Industrial Research | An intensified process of synthesis of dialkyl ethers using a step conical reactor |
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