US2912475A - Manufacture of low molecular unsaturated hydrocarbons - Google Patents

Manufacture of low molecular unsaturated hydrocarbons Download PDF

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US2912475A
US2912475A US578581A US57858156A US2912475A US 2912475 A US2912475 A US 2912475A US 578581 A US578581 A US 578581A US 57858156 A US57858156 A US 57858156A US 2912475 A US2912475 A US 2912475A
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gas
oxygen
carrier gas
temperature
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Krause Walter
Krekeler Hans
Wirtz Rudolf
Kamptner Herbert
Bachmann Ditmar
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Hoechst AG
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/35Formation of carbon-to-carbon triple bonds only
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/76Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation of hydrocarbons with partial elimination of hydrogen
    • C07C2/78Processes with partial combustion
    • 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
    • C10G47/00Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
    • C10G47/36Controlling or regulating
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/34Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts
    • C10G9/36Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts with heated gases or vapours
    • 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
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B3/00Engines characterised by air compression and subsequent fuel addition
    • F02B3/06Engines characterised by air compression and subsequent fuel addition with compression ignition

Definitions

  • the hot combustion gases from an oxyhydrogen flame are used as a carrier; these gases are mixed in a nozzle with a hydrocarbon that is gaseous at room temperature andunder normal pressure, and the mixture of gases is chilled after a short time of reaction.
  • this process involves the disadvantage that thevhot combustion gases of the oxyhydrogen flame contain a considerable proportion of oxygen-containing radicals, oxygen atoms and oxygen molecules which react with part of the hydro carbon to form carbon monoxide and carbon dioxide.
  • Our present invention provides a process for the manufacture of low molecular unsaturated aliphatic hydrocarbons, especially acetylene and/or ethylene, in which a hydrocarbon containing at least two carbon atoms is pyrolized by contacting it for a short time with a carrier gas consisting of hot combustion gas containing hydrogen, wherein the oxygenand oxygen-containing radicals, oxygen atoms and oxygen molecules which are formed by dissociation and-are contained in the hot combustion gas are first recombined by the introduction of at least one secondary gas having a lower temperature than the combustion gas and which is advantageously of the same chemical nature as the combustion gas,
  • the amount of the hydrocarbon introduced is so selected that the temperature of the gas mixture still amounts to at least 700 C. after the gas has been mixed and reacted with the hydrocarbon and prior to the chilling of the reaction mixture obtained.
  • hydrocarbons there are used aliphatic hydrocarbons.
  • hydrocarbons which are liquid at room temperature there can advantageously be used any hydrocarbons, such as hexanes, he'ptanes, octanes, decanes, the mono-unsaturated aliphatic hydrocarbons, commercial mixtures of hydrocarbons, such as petroleum distillates, fractions of benz'ine, topped oils, diesel oils etc.
  • the process according to this invention can be conducted with particular advantage without application of superatmospheric pressure. It is, however, also possible toperform the pyrolysis both with application of elevated pressure or under sli htly reduced pressure.
  • Ascarrier gas there maybe used with advantage the combustion-gases of oils, coal dust, gaseous hydrocarbons, hydrogen, etc. to which freehydrogen is added, if not yet contained in these compounds.
  • As' carrier gas there may also be used mixtures of hydrogen with steam and carbon monoxide, if desired in admixture with carbon dioxide or small amounts of other-substances which do not affect the reaction and as obtained by combustion of the aforesaid substances orAby-the addition of hydrogen.
  • carrier gas nitrogen or carbon dioxide alone or gas mixtures rich in nitrogen or carbon dioxide.
  • secondary gases there may also be used the gases that are formed by the combustion of the substances described in the preceding paragraph.
  • steam it has proved to be particularly advantageous to use steam as carrier gas, and to use steam and/or hydrogen as secondary gas.
  • the hydrogen can be introduced into the carrier gas at any temperature desired; if, however, steam is used as a secondary gas, such steam is required to have a temperature which at least corresponds to the boiling point of the water under the corresponding pressure.
  • mixtures of steam or mixtures of steam and hydrogen it is, however, advantageous to introduce these mixtures at a temperature of at least 150 C.
  • the quantity of the secondary gas used may vary within wide limits; furthermore, the amount is dependent on the temperature of the carrier gas and the secondary gas.
  • the amount of the secondary gas used generally, amounts to bet-ween 1 and 80 percent by weight, preferably 30 to 70 percent by weight, and is in each case calculated upon the sum of carrier gas and secondary gas.
  • the hydrocarbon is introduced according to methods known per se; it is preferable to introduce the hydrocarbons at a temperature not in excess of 400 C., so that no cracking occurs prior to the reaction. It is, however, also possible to introduce liquid hydrocarbons by injection.
  • the carrier gas is produced, as has already been mentioned above, by combustion of a combustible substance immediately before contacting the hydrocarbon.
  • a nozzle is arranged between the combustion flame and the reaction chamber, it being of advantage to mix the hydrocarbon with the gas used as carrier gas immediately behind that nozzle.
  • the propellant has a temperature of about 2200" C. and, when it is mixed with said hydrocarbons, a temperature of about 1650 C. At 2200" C. there are still present noteworthy quantities of oxygencontaining radicals, oxygen atoms and oxygen molecules which favour the formation of carbon monoxide from the hydrocarbons to be reacted.
  • the gases to be reacted are preheated on the filling material to temperatures of about 1000 C. and more prior to being mixed up, whereby distinct cracking occurs.
  • This process is very complicated and can only be conducted, if at all, with the use of hydrocarbons which are gaseous at room temperature because of the high temperatures required for pre-heating and owing to the special mode of pre-heating the aforesaid hydrocarbons which are to be reacted; this pre-heating operation involves pumping the cooled filling material into a second container to be heated up.
  • EXAMPLE 1 (A) To the hot combustion gases obtained by'combustion, per hour, of 26 normal cubic metres (cubic metreat 0 C. under atmospheric pressure) of hydrogen and 12 normal cubic metres of oxygen, ethylene is added in an amount such that the temperature in the reaction zone is about 1100 to 1300 C. The gases are reacted within about 0.005 second and then chilled.
  • EXAMPLE 4 Under the conditions applied in Example 3 are reacted the same amounts of hydrogen, oxygen and hydrocarbons of the same petroleum fraction (boiling range: 54360 C.) with the exception, however, that the combustion gases are mixed, per hour, with 19.5 kilograms of steam prior to being mixed up with the hydrocarbons.
  • a process for the manufacture of low molecular weight unsaturated aliphatic hydrocarbons which comprises (a) forming a stream of hot combustion gas containing oxygen atoms, oxygen molecules and oxygencontaining radicals formed by dissociation; (b) introducing a secondary gas into said stream of hot combustion gas for recombining the oxygen atoms, oxygen molecules and oxygen-containing radicals therein and thereby form-' ing a stream of carrier gas which is substantially free from molecular oxygen and contains hydrogen, said secondary gas having a temperature of at least about 150 C. but a lower temperature than the combustion gas and the amount thereof being about 1 to 80% by weight,
  • a process for the manufacture of low molecular weight unsaturated aliphatic hydrocarbons rich in unsaturated C hydrocarbons which comprises (a) forming a stream of hot combustion gas obtained by combustion of an excess of hydrogen with oxygen and containing oxygen atoms, oxygen molecules and oxygen-containing radicals formed by dissociation; (b) introducing a secondary gas into said stream of hot combustion gas for recombining the oxygen atoms, oxygen molecules and oxygen-containing radicals therein and thereby forming a stream of carrier gas which is substantially free from molecular oxygen and contains hydrogen, said secondary gas being selected from the group consisting of hydrogen, steam and mixtures thereof and having a temperature of at least about 150 C.
  • a process for the manufacture of low molecular weight unsaturated aliphatic hydrocarbons rich in acetylene which comprises (a) forming a stream of hot combustion gas obtained by combustion of an excess of hydrogen with oxygen and containing oxygen atoms, oxygen molecules and oxygen-containing radicals formed by dissociation; (b) introducing a secondary gas into said stream of hot combustion gas for recombining the oxygen atoms, oxygen molecules and oxygen-containing radicals therein and thereby forming a stream of carrier gas which is substantially free from molecular oxygen and contains hydrogen, said secondary gas being selected from the group consisting of hydrogen, steam and mixtures thereof and having a temperature of at least about 150 C.
  • a process according to claim 1, wherein the hydrocarbon to be pyrolized is liquid at room temperature and g is contacted with the combustion gas in the geaseous state.
  • a combustion gas which consists substantially of a mixture of steam, hydrogen and carbon monoxide.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Description

United States Patent MANUFACTURE OF LOW MOLECULAR UNSATURATED HYDROCARBONS Walter Krause, Frankfurt am Main, Hans Krekeler, Ko-
nigstein (Taunus), and Rudolf Wirtz and Herbert Kamptner, Frankfurt am Main, and Ditmar Bachmann, Hofheim (Taunus), Germany, assignors to Farbwerke Hoechst Aktiengesellschaft vormals Meister Lucius &
Briining, Frankfurt am Main, Germany, a corporation of Germany 1 N0 Drawing. Application April 17, 1956 Serial No. 578,581
Claims priority, application Germany April 28, 1955 14 Claims. (Cl. 260-679) Various processes have already been described which relate to the, production of low molecular unsaturated hydrocarbons, wherein gaseous or liquid hydrocarbons are reacted with a carrier gas at high temperatures. As carrier gas it has been proposed to use, for example, steam. In these known processes, the gas used as a carrier has been heated in various ways to a high temperature Thus, for example, a tower filled with ceramic material is first heated by combustion gases of carboncontaining compounds and, when the combustion is terminated, the tower is cleansed by means of inert gases, e.g. steam, so as to remove the combustion gases and the steam is then heated up on the heated ceramic material. This process, however, involves the disadvantage that the steam temperature varies during the cracking process and diminishes in each period until the heating tower must again be heated up; therefore, a non-uniform reaction product is always obtained. This process, furthermore, requires thorough and constant control and involves great losses in energy.
According to another known process, the hot combustion gases from an oxyhydrogen flame are used as a carrier; these gases are mixed in a nozzle with a hydrocarbon that is gaseous at room temperature andunder normal pressure, and the mixture of gases is chilled after a short time of reaction. However, this process involves the disadvantage that thevhot combustion gases of the oxyhydrogen flame contain a considerable proportion of oxygen-containing radicals, oxygen atoms and oxygen molecules which react with part of the hydro carbon to form carbon monoxide and carbon dioxide.
Our present invention provides a process for the manufacture of low molecular unsaturated aliphatic hydrocarbons, especially acetylene and/or ethylene, in which a hydrocarbon containing at least two carbon atoms is pyrolized by contacting it for a short time with a carrier gas consisting of hot combustion gas containing hydrogen, wherein the oxygenand oxygen-containing radicals, oxygen atoms and oxygen molecules which are formed by dissociation and-are contained in the hot combustion gas are first recombined by the introduction of at least one secondary gas having a lower temperature than the combustion gas and which is advantageously of the same chemical nature as the combustion gas,
introduction of the less heated gas is used for heating up the secondary-gas and the dissociation energy contained in the carrier gas used is converted to kinetic energy. It-has been found that the oxygen-containing radicals, the oxygen atoms andthe oxygen molecules -contained in the carrier gas favour the formation of carbon monoxide and carbon dioxide in the subsequentin the conventional time of reaction which, preferably,
amounts to 10* to 10- seconds, and prior to the chilling of the reaction mixture.
When it is desired to produce ethylene as the main product, it is advisable to effect the reaction within. 10' to 10- seconds; in this case, the amount of the hydrocarbon introduced is so selected that the temperature of the gas mixture still amounts to at least 700 C. after the gas has been mixed and reacted with the hydrocarbon and prior to the chilling of the reaction mixture obtained. When, however, it is desired to produce acetylene asthe main product, it is advantageous to perform thc'reaction within a shorter time, i.e. within 10; to 10- seconds, and so to select the amount of the hydrocarbon introduced that the temperature of the gas mixture still amounts to at least 1000" C., after the gas has been mixed and reacted with the hydrocarbon or hydrocarbons and prior to the chilling of the reaction mixture obtained.
As starting hydrocarbons there are used aliphatic hydrocarbons. As such compounds there may be mentioned, more especially, ethane, propane, butane, ethylene, propylene, the butylenes and commercial mixtures of these gases; as hydrocarbons which are liquid at room temperature there can advantageously be used any hydrocarbons, such as hexanes, he'ptanes, octanes, decanes, the mono-unsaturated aliphatic hydrocarbons, commercial mixtures of hydrocarbons, such as petroleum distillates, fractions of benz'ine, topped oils, diesel oils etc. There can also be used hydrocarbons which are sol-id at room temperature and contain up to 30 or more carbon atoms; these latter compounds are adgaseous state With a current of combustion gases which are free from oxygen and contain hydrogen.
The process according to this invention can be conducted with particular advantage without application of superatmospheric pressure. It is, however, also possible toperform the pyrolysis both with application of elevated pressure or under sli htly reduced pressure. A It is advisable to introduce the secondary gas under a pressure of at least 1 atmosphere '(absolute). However, itis advantageous to introduce the secondary gas at least under-the same pressure as prevails at the inlet where the carriergasf is introduced. 1
Ascarrier gas there maybe used with advantage the combustion-gases of oils, coal dust, gaseous hydrocarbons, hydrogen, etc. to which freehydrogen is added, if not yet contained in these compounds. As' carrier gas there may also be used mixtures of hydrogen with steam and carbon monoxide, if desired in admixture with carbon dioxide or small amounts of other-substances which do not affect the reaction and as obtained by combustion of the aforesaid substances orAby-the addition of hydrogen. In the preparation of acetylene it is, generally, not advisable to use as carrier gas nitrogen or carbon dioxide alone or gas mixtures rich in nitrogen or carbon dioxide. These mixtures exhibit a detrimental effect, that is, in the presence of carbon dioxide it is especially the subsequent separation of the gas that is rendered diflicult, and in the presence of nitrogen the formation of acetylene is retarded.
As secondary gases there may also be used the gases that are formed by the combustion of the substances described in the preceding paragraph. For the purpose of this invention, it has proved to be particularly advantageous to use steam as carrier gas, and to use steam and/or hydrogen as secondary gas. If hydrogen is used as secondary gas, the hydrogen can be introduced into the carrier gas at any temperature desired; if, however, steam is used as a secondary gas, such steam is required to have a temperature which at least corresponds to the boiling point of the water under the corresponding pressure. When mixtures of steam or mixtures of steam and hydrogen are used, it is, however, advantageous to introduce these mixtures at a temperature of at least 150 C.
The quantity of the secondary gas used may vary within wide limits; furthermore, the amount is dependent on the temperature of the carrier gas and the secondary gas. The amount of the secondary gas used, generally, amounts to bet-ween 1 and 80 percent by weight, preferably 30 to 70 percent by weight, and is in each case calculated upon the sum of carrier gas and secondary gas.
The hydrocarbon is introduced according to methods known per se; it is preferable to introduce the hydrocarbons at a temperature not in excess of 400 C., so that no cracking occurs prior to the reaction. It is, however, also possible to introduce liquid hydrocarbons by injection.
In the process of this invention the carrier gas is produced, as has already been mentioned above, by combustion of a combustible substance immediately before contacting the hydrocarbon. To this end, it is advisable to provide for a fairly small distance between the combustion flame and the reaction chamber in order to keep the heat losses caused by dissipation as limited as possible. Preferably a nozzle is arranged between the combustion flame and the reaction chamber, it being of advantage to mix the hydrocarbon with the gas used as carrier gas immediately behind that nozzle.
The significance of the process steps according to the invention is apparent from the fact that in a hot current of steam of 2000" C. about 1.0 percent by volume of steam is present in the form of the OH-radical, 1.0 percent by volume in the form of the O -molecule, and 0.06 percent by volume in the form of the oxygen atom. At a temperature of 2850 C. which is the temperature of the oxyhydrogen flame without admixture of secondary steam, the OH-radicals, O-radicals and O -mlecules are present in a proportion of 11.5:4.5:5.8 percent by volume. It will be understood that the higher the temperature of the combustion gas, the greater is the advantage offered by the process of this invention.
It has already been proposed to mix a superheated carrier gas with heated methane, ethane or propane in a nozzle and to react the mixture obtained in a reactor. In this known process the propellant has a temperature of about 2200" C. and, when it is mixed with said hydrocarbons, a temperature of about 1650 C. At 2200" C. there are still present noteworthy quantities of oxygencontaining radicals, oxygen atoms and oxygen molecules which favour the formation of carbon monoxide from the hydrocarbons to be reacted. Besides, according to this known process, the gases to be reacted are preheated on the filling material to temperatures of about 1000 C. and more prior to being mixed up, whereby distinct cracking occurs. This process is very complicated and can only be conducted, if at all, with the use of hydrocarbons which are gaseous at room temperature because of the high temperatures required for pre-heating and owing to the special mode of pre-heating the aforesaid hydrocarbons which are to be reacted; this pre-heating operation involves pumping the cooled filling material into a second container to be heated up.
The following examples serve to illustrate the invention, but they are not intended to limit it thereto:
EXAMPLE 1 (A) To the hot combustion gases obtained by'combustion, per hour, of 26 normal cubic metres (cubic metreat 0 C. under atmospheric pressure) of hydrogen and 12 normal cubic metres of oxygen, ethylene is added in an amount such that the temperature in the reaction zone is about 1100 to 1300 C. The gases are reacted within about 0.005 second and then chilled.
(B) The same amounts of hydrogen, oxygen and ethylene are reacted as indicated sub A with the exception, however, that, per hour, 9 kilograms of steam are added prior to the mixing operation with ethylene.
(C) The reaction tower is charged with the same amounts of oxygen, hydrogen and ethylene as indicated sub A and B with the exception, however, that, per hour, 35 kilograms of steam are added prior to the mixing operation with ethylene. The test results obtained are indicated in the following table. The quantities determined by analysis are given in percent by volume:
Table Steam intro- Steam intro- Wlthout steam duced, 9 kilodnced, 35 kilograms/hour grams/hour EXAMPLE 2 To the hot combustion gases obtained by combustion, per hour, of 27.5 normal cubic metres of hydrogen and 13.5 normal cubic metres of oxygen are added first 19.5 kilograms of steam of 180 C. and immediately thereafter benzine (boiling range: 50220 C.; superheated to 350 C.) in an amount such that the temperature in the reaction zone amounts to 11001300 C. The components are reacted in the reaction zone for 0.002 second and the reaction mixture is chilled.
From the benzine introduced is obtained percent of a gaseous product of the following composition, (Quantities in percent by volume): 0.8% of CO 17.0% of acetylene, 0.8% of higher unsaturated hydrocarbons, 14.9% of ethylene, 9.1% of carbon monoxide, 44.8% of hydrogen and 12.6% of saturated hydrocarbons consisting substantially of methane.
EXAMPLE 3 To the hot combustion gases obtained by combustion, per hour, of 27.5 normal cubic metres of hydrogen and 13.5 normal cubic metres of oxygen are added, per hour, 3 kilograms of steam of C. and immediately there after a petroleum fraction (boiling range: 54360 C.; superheated to 400 C.) in an amount such that the temperature in the reaction zone amounts to 1100-1300 C. The components are reacted in the reaction zone within 0.002 second and the reaction mixture obtained is chilled.
From the petroleum fraction used is obtained 78.5 percent of a gaseous product of the following composition (quantities in percent by volume): 2.1% of CO 15.1% of acetylene, 0.8% of higher unsaturated hydrocarbons, 11.8% of ethylene, 9.9% of carbon monoxide,
47.5% of hydrogen, and 12.8% of unsaturated hydrocarbons.
EXAMPLE 4 Under the conditions applied in Example 3 are re acted the same amounts of hydrogen, oxygen and hydrocarbons of the same petroleum fraction (boiling range: 54360 C.) with the exception, however, that the combustion gases are mixed, per hour, with 19.5 kilograms of steam prior to being mixed up with the hydrocarbons.
From the petroleum fraction used is obtained 76 percent of a gaseous product of the following composition (quantities in percent by volume): 1.6% of CO 17.5% of acetylene, 13.9% of ethylene, 8.8% of carbon monoxide, 45.6% of hydrogen and 12.6% of saturated hydrocarbons.
What we claim is:
l. A process for the manufacture of low molecular weight unsaturated aliphatic hydrocarbons which comprises (a) forming a stream of hot combustion gas containing oxygen atoms, oxygen molecules and oxygencontaining radicals formed by dissociation; (b) introducing a secondary gas into said stream of hot combustion gas for recombining the oxygen atoms, oxygen molecules and oxygen-containing radicals therein and thereby form-' ing a stream of carrier gas which is substantially free from molecular oxygen and contains hydrogen, said secondary gas having a temperature of at least about 150 C. but a lower temperature than the combustion gas and the amount thereof being about 1 to 80% by weight,
calculated upon the total amount of carrier gas;
passing the carrier gas through a restricted opening into a reaction zone for accelerating said stream of carrier gas; and (d) contacting the accelerated stream of carrier gas with a hydrocarbon containing at least two carbon atoms in the molecule for to 10- seconds for pyrolysis of said hydrocarbon, the rate of feed of hydrocarbon being adjusted to maintain the temperature of the reacted gas mixture at at least about 700 C.
2. A process for the manufacture of low molecular weight unsaturated aliphatic hydrocarbons rich in unsaturated C hydrocarbons which comprises (a) forming a stream of hot combustion gas obtained by combustion of an excess of hydrogen with oxygen and containing oxygen atoms, oxygen molecules and oxygen-containing radicals formed by dissociation; (b) introducing a secondary gas into said stream of hot combustion gas for recombining the oxygen atoms, oxygen molecules and oxygen-containing radicals therein and thereby forming a stream of carrier gas which is substantially free from molecular oxygen and contains hydrogen, said secondary gas being selected from the group consisting of hydrogen, steam and mixtures thereof and having a temperature of at least about 150 C. but a lower temperature than the combustion gas and the amount thereof being about 1 to 80% by weight, calculated upon the total amount of carrier gas; (c) passing the carrier gas through a restricted opening into a reaction zone for accelerating said stream of carrier gas; and (d) contacting the accelerated stream of carrier gas with a hydrocarbon that is liquid at room temperature for 10- to 10- seconds for pyrolysis of said hydrocarbon, the rate of feed of hydrocarbon being adjusted to maintain the temperature I of the reacted gas mixture at at least about 700 C.
3. A process for the manufacture of low molecular weight unsaturated aliphatic hydrocarbons rich in acetylene which comprises (a) forming a stream of hot combustion gas obtained by combustion of an excess of hydrogen with oxygen and containing oxygen atoms, oxygen molecules and oxygen-containing radicals formed by dissociation; (b) introducing a secondary gas into said stream of hot combustion gas for recombining the oxygen atoms, oxygen molecules and oxygen-containing radicals therein and thereby forming a stream of carrier gas which is substantially free from molecular oxygen and contains hydrogen, said secondary gas being selected from the group consisting of hydrogen, steam and mixtures thereof and having a temperature of at least about 150 C. but a lower temperature than the combustion gas and the amount thereof being about 1 to 80% by weight, calculated upon the total 7 amount of carrier gas; (0) passing the carrier gas through a restricted opening into a reaction zone for accelerating said stream of carrier gas; and (d) contacting the accelerated stream of carrier gas with a hydrocarbon that is liquid at room temperature for 10- to 10 seconds for pyrolysis of said hydrocarbon, the rate of feed of hydrocarbon being adjusted to maintain the temperature of the reacted gas mixture at at least about 1000 C.
4. A process as defined in claim 1 wherein steam is present in the secondary gas and said secondary gas has in addition a temperature at least equal to the boiling temperature of water under the conditions of operation.
5. A process according to claim 1, wherein the hydrocarbons to be pyrolized are preheated before they are contacted with the combustion gas.
6. A process according to claim 1, wherein ethylene is produced as a main product by adjusting the temperature of the gas mixture after the reaction within 10' to 10- sec., to at least 700 C. by regulating the amount of the hydrocarbon to be pyrolized.
7. A'process according to claim 1, wherein the reaction is carried out substantially at atmospheric pressure.
8. A process according to claim 1, wherein the secondary gas is introduced under a pressure of at least 1 atmosphere.
9. A process according to claim 1, wherein the secondary gas is a compound selected from the group consisting of hydrogen, steam and mixtures thereof.
10. A process according to claim 1, wherein the secondary gas is used in an amount of 30-70% by weight, calculated upon the total amount of combustion gas and secondary gas.
11. A process according to claim 1, wherein a combustion gas is used which consists substantially of steam.
12. A process according to claim 1, wherein the hydrocarbon to be pyrolized is liquid at room temperature and g is contacted with the combustion gas in the geaseous state.
13. A process according to claim used as secondary gas.
14. *A process accordingto to claim 1, wherein a combustion gas is used which consists substantially of a mixture of steam, hydrogen and carbon monoxide.
1, wherein steam is References Cited in the file of this patent UNITED STATES PATENTS Robinson Feb. 11,1958

Claims (1)

  1. 3. A PROCESS FOR THE MANUFACTURE OF LOW MOLECULAR WEIGHT UNSATURATED ALIPHATIC HYDROCARBONS RICH IN ACETYLENE WHICH COMPRISES (A) FORMING A STREAM OF HOT COMBUSTION GAS OBTAINED BY COMBUSTION OF AN EXCESS OF HYDROGEN WITH OXYGEN AND CONTAINING OXYGEN ATOMS, OXYGEN MOLECULES AND OXYGEN-CONTAINING RADICALS FORMED BY DISSOCIATION; (B) INTRODUCING A SECONDARY GAS INTO SAID STREAM OF HOT COMBUSTION GAS FOR RECOMBINING THE OXYGEN ATOMS, ATOMS, OXYGEN MOLECULES AND OXYGEN-CONTAINING RADICALS THEREIN AND THEREBY FORMING A STREAM OF CARRIER GAS WHICH IS SUBSTANIALLY FREE FROM MOLECULAR OXYGEN AND CONTAINS HYDROGEN, SAID SECONDARY GAS BEING SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, STEAM AND MIXTURE THEREOF AND HAVING A TEMPERATURE OF AT LEAST ABOUT 150* C. BUT A LOWER TEMPERATURE THAN THE COMBUSTION GAS AND THE AMOUNT THEREOF BEING ABOUT 1 TO 8% BY WEIGHT, CALCULATED UPON THE TOTAL AMOUNT OF CARRIER GAS; (C) PASSING THE CARRIER GAS THROUGH A RESTRICTED OPENING INTO A REACTION ZONE FOR ACCELERATING SAID STREAM OF CARRIER GAS; AND (D) CONTACTING THE ACCELERATED STREAM OF CARRIER GAS WITH A HYDROCARBON THAT IS LIQUID AT ROOM TEMPERATURE FOR 10-2 TO 10-4 SECONDS FOR PYROLSIS OF SAID HYDROCARBON, THE RATE OF FEED OF HYDROCARBON BEING ADJUSTED TO MAINTAINED THE TEMPERATURE OF THE REACTED GAS MIXTURE AT AT LEASTE ABOUT 1000* C.
US578581A 1955-04-28 1956-04-17 Manufacture of low molecular unsaturated hydrocarbons Expired - Lifetime US2912475A (en)

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US3019271A (en) * 1958-09-08 1962-01-30 Belge Produits Chimiques Sa Process and apparatus for treatment of hydrocarbons
US3116343A (en) * 1960-08-19 1963-12-31 Shell Oil Co Temperature-stabilized conversion of hydrocarbons and the like
US3116344A (en) * 1960-08-19 1963-12-31 Shell Oil Co Vortex tube reactor and process for converting hydrocarbons therein
US3129266A (en) * 1961-09-11 1964-04-14 Messrs Kogyokaihatsu Process for production of acetylene by thermal decomposition of hydrocarbons
US3180904A (en) * 1959-05-15 1965-04-27 Hoechst Ag Process for the manufacture of olefins
US3240836A (en) * 1960-06-21 1966-03-15 Hoechst Ag Process for cracking hydrocarbons
US3270076A (en) * 1965-10-28 1966-08-30 Nat Lead Co Propylene cracking
US4206032A (en) * 1978-03-17 1980-06-03 Rockwell International Corporation Hydrogenation of carbonaceous materials
US4256565A (en) * 1979-11-13 1981-03-17 Rockwell International Corporation Method of producing olefins from hydrocarbons
US4536603A (en) * 1983-12-22 1985-08-20 Rockwell International Corporation Production of acetylene from coal by contact with a combustion gas
US4724272A (en) * 1984-04-17 1988-02-09 Rockwell International Corporation Method of controlling pyrolysis temperature
US11123705B1 (en) 2018-10-23 2021-09-21 Sabic Global Technologies B.V. Method and reactor for conversion of hydrocarbons

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CA835434A (en) * 1964-11-09 1970-02-24 Happel John Pyrolysis of hydrocarbons
GB1504776A (en) * 1975-08-14 1978-03-22 Davy Powergas Ltd Hydrocracking c3 or higher hydrocarbon feedstock
DE3173086D1 (en) * 1981-03-09 1986-01-16 Dow Chemical Co Crude oil cracking using partial combustion gases
JPS59152992A (en) * 1983-02-18 1984-08-31 Mitsubishi Heavy Ind Ltd Thermal decomposition for producing olefin from hydrocarbon
JPS59159887A (en) * 1983-03-03 1984-09-10 Mitsubishi Heavy Ind Ltd Thermal cracking of hydrocarbon to produce olefin
JPS6011585A (en) * 1983-06-30 1985-01-21 Mitsubishi Heavy Ind Ltd Thermal cracking to produce petrochemicals selectively from hydrocarbon
JPS6011584A (en) * 1983-06-30 1985-01-21 Mitsubishi Heavy Ind Ltd Thermal cracking to produce petrochemicals selectively from hydrocarbon
US4982039A (en) * 1987-09-03 1991-01-01 University Of Southern California Conversion of halogenated toxic substances

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US2520149A (en) * 1944-06-14 1950-08-29 Koppers Co Inc Process for producing olefins
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US2816941A (en) * 1953-11-27 1957-12-17 Phillips Petroleum Co Production of unsaturated hydrocarbons and apparatus therefor
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US2520149A (en) * 1944-06-14 1950-08-29 Koppers Co Inc Process for producing olefins
US2706210A (en) * 1950-12-05 1955-04-12 Wulff Process Company Process suitable for converting primary hydrocarbons to secondary hydrocarbons
US2767233A (en) * 1952-01-07 1956-10-16 Chemical Construction Corp Thermal transformation of hydrocarbons
US2816941A (en) * 1953-11-27 1957-12-17 Phillips Petroleum Co Production of unsaturated hydrocarbons and apparatus therefor
US2823243A (en) * 1956-03-19 1958-02-11 Phillips Petroleum Co Process and apparatus for pyrolysis of hydrocarbons

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3019271A (en) * 1958-09-08 1962-01-30 Belge Produits Chimiques Sa Process and apparatus for treatment of hydrocarbons
US3180904A (en) * 1959-05-15 1965-04-27 Hoechst Ag Process for the manufacture of olefins
US3240836A (en) * 1960-06-21 1966-03-15 Hoechst Ag Process for cracking hydrocarbons
US3116343A (en) * 1960-08-19 1963-12-31 Shell Oil Co Temperature-stabilized conversion of hydrocarbons and the like
US3116344A (en) * 1960-08-19 1963-12-31 Shell Oil Co Vortex tube reactor and process for converting hydrocarbons therein
US3129266A (en) * 1961-09-11 1964-04-14 Messrs Kogyokaihatsu Process for production of acetylene by thermal decomposition of hydrocarbons
US3270076A (en) * 1965-10-28 1966-08-30 Nat Lead Co Propylene cracking
US4206032A (en) * 1978-03-17 1980-06-03 Rockwell International Corporation Hydrogenation of carbonaceous materials
US4256565A (en) * 1979-11-13 1981-03-17 Rockwell International Corporation Method of producing olefins from hydrocarbons
FR2469446A1 (en) * 1979-11-13 1981-05-22 Rockwell International Corp PROCESS FOR THE RAPID PRODUCTION OF OLEFINS BY THERMAL CONVERSION OF HYDROCARBONS IN THE PRESENCE OF HYDROGEN
US4536603A (en) * 1983-12-22 1985-08-20 Rockwell International Corporation Production of acetylene from coal by contact with a combustion gas
US4724272A (en) * 1984-04-17 1988-02-09 Rockwell International Corporation Method of controlling pyrolysis temperature
US11123705B1 (en) 2018-10-23 2021-09-21 Sabic Global Technologies B.V. Method and reactor for conversion of hydrocarbons

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DE1114182B (en) 1961-09-28
GB823956A (en) 1959-11-18
BE547407A (en)
FR1161043A (en) 1958-08-19

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