USRE19794E - Preparation of acetylene - Google Patents
Preparation of acetylene Download PDFInfo
- Publication number
- USRE19794E USRE19794E US19794DE USRE19794E US RE19794 E USRE19794 E US RE19794E US 19794D E US19794D E US 19794DE US RE19794 E USRE19794 E US RE19794E
- Authority
- US
- United States
- Prior art keywords
- acetylene
- methane
- reaction
- temperatures
- furnace
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 title description 16
- 238000002360 preparation method Methods 0.000 title description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 14
- 239000007789 gas Substances 0.000 description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 230000001131 transforming Effects 0.000 description 4
- 239000004020 conductor Substances 0.000 description 3
- 238000010494 dissociation reaction Methods 0.000 description 3
- 230000005593 dissociations Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N acetylene Chemical compound C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- YZCKVEUIGOORGS-IGMARMGPSA-N protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/76—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation of hydrocarbons with partial elimination of hydrogen
Definitions
- This invention relates to the art of treating methane and other hydrocarbons for the preparation of acetylene and hydrogen.
- methane gas has been heated to high temperatures for the production of lamp black or soot, in which processes the methane is said to be completely decomposed into carbon and hydrogen.
- the heating has thus split up the methane into its elemental components. If any intermediate products are formed, they are apparently decomposed before leaving the furnace.
- 2CH 2C H +3H (1) depends on the contact between the quantity of methane and the surface heated to temperatures higher than the temperature for total dissociation of methane, i. e., for practical purposes, between 1400 and 2000 C.
- the process is carried out in the main by passing the gas, either preheated or not, through an electric furnace with carbon electrodes.
- the interior of the furnace is filled with pieces of carbon irregularly broken up, or of some uniform shape but of different sizes.
- an electric furnace with elec trodes of carbon fragments I obtained a yield of about of acetylene (exactly 68.8%).
- the yield in the transformation of methane into acetylene can be increased if one uses as resistances in the electric furnace any variety of carbon or material which contains carbon and is good conductor of electricity, or any other material which has a large contact surface and is made an electrical conductor by one of the known means and is raised to and kept at the temperatures necessary for the reaction, 1. e. temperatures higher than 1400" C.
- any porous material which can withstand the temperatures mentioned above, at which the reaction (1) takes place.
- This material may, or may not be a conductor of electricity.
- the gases should be preheated.
- the heated gases should flow into the furnace directly into a zone higher in temperature than 1400 C.
- a reduced pressure produced by an exhauster should be maintained in the furnace to help the transformation of methane into acetylene and hydrogen 1. e. to increase the yield.
- acetylene one is not obliged to prepare it only from methane.
- acetylene In the manufacture of acetylene, the process which comprises passing a gas, selected from a class consisting of methane and gases containing a substantial quantity of methane, into a reaction zone, maintained at temperatures ranging from about 1400 C. to 2000 C. and in the absence oi air, and exhausting the acetylene-containing reaction products from the reaction zone thereby producing a reduced pressure in said zone.
- a gas selected from a class consisting of methane and gases containing a substantial quantity of methane
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
SPAS-3.5: c
Reissued Dec. 24, 1935 'UNITED STATES kxammer PREPARATION OF ACETYLENE Martin Banck, Bucharest, Rumania, assignor to Ruhrchemie Aktiengesellschaft, Oberhausen- Holten, Germany, a corporation of Germany No Drawing. Original No. 1,773,611, dated August 19, 1930, Serial No. 172,561, March 3, 1927. Application for reissue August 5, 1932, Serial No. 627,601, and in Germany March 15, 1926 3 Claims.
This invention relates to the art of treating methane and other hydrocarbons for the preparation of acetylene and hydrogen.
According to certain prior processes, methane gas has been heated to high temperatures for the production of lamp black or soot, in which processes the methane is said to be completely decomposed into carbon and hydrogen. The heating has thus split up the methane into its elemental components. If any intermediate products are formed, they are apparently decomposed before leaving the furnace.
It has also been reported in the literature that, upon the heating of hydrocarbons, such as methane, acetylene is first formed but that at higher temperatures this splits up directly into carbon and hydrogen; see, for example, Prof. Lewes article in Proc. Royal Soc. London, 55, 91-107 (1894). This article states that the acetylene first formed polymerizes to form benzene, etc. at relatively low temperatures but that it "decomposes at about 1200 C. with liberation of carbon, indicating that at temperatures much above this decomposition point it is impossible to obtain any substantial yields of acetylene. I have found, on the contrary, that much larger yields of acetylene can be obtained at higher temperatures by exhausting the reaction products from the reaction zone or by preventing dissociation of the acetylene by diluting the reaction gases with other inert gases. By these means a subatmospheric pressure of methane is obtained in the reaction zone.
I have established by systematic experiments that the yield from the well known reaction:
2CH 2C H +3H (1) depends on the contact between the quantity of methane and the surface heated to temperatures higher than the temperature for total dissociation of methane, i. e., for practical purposes, between 1400 and 2000 C.
The yield from this reaction of methane into acetylene and hydrogen increases and approximates more closely the theoretical yield in proportion to the extent of the surface of contact.
In other words, it is dependent on the extent to which the whole of the gas is brought into contact with the surfaces heated to the temperatures necessary for the reaction.
The process is carried out in the main by passing the gas, either preheated or not, through an electric furnace with carbon electrodes. In order to get a greater contact surface the interior of the furnace is filled with pieces of carbon irregularly broken up, or of some uniform shape but of different sizes. In an electric furnace with elec trodes of carbon fragments I obtained a yield of about of acetylene (exactly 68.8%).
I have further found that the yield in the transformation of methane into acetylene can be increased if one uses as resistances in the electric furnace any variety of carbon or material which contains carbon and is good conductor of electricity, or any other material which has a large contact surface and is made an electrical conductor by one of the known means and is raised to and kept at the temperatures necessary for the reaction, 1. e. temperatures higher than 1400" C.
I have also found that one can use in the furnace as contact mass, any porous material which can withstand the temperatures mentioned above, at which the reaction (1) takes place. This material may, or may not be a conductor of electricity.
By varying the resistance in the electric furnace, the consumption of almost 1 kw/hr. which had been found necessary for the transformation of a cubic meter of methane, can be reduced to about kw/hr., for the same quantity.
I have noticed and determined experimentally that to increase and maintain the contact surface at the necessary reaction temperatures one can employ other electric furnaces, or other means of heating without resistances.
I have found that it is possible to employ for the same purpose, and with the same result, an arc furnace with the are expanded by a magnetic field or by a strong current of gas.
In all cases one must pay scrupulous attention to the tightness of the apparatus so as to prevent any access of air. It is also absolutely necessary to prevent the diffusion of hydrogen which is necessary for maintaining the stability of the acetylene at temperatures lower than the temperatures of formation of this hydrocarbon.
By experience I have found that the following things are advantageous to assure the greatest yield from this reaction and to keep the furnace in continuous operation:
1. The gases should be preheated.
2. The heated gases should flow into the furnace directly into a zone higher in temperature than 1400 C.
3. A reduced pressure produced by an exhauster should be maintained in the furnace to help the transformation of methane into acetylene and hydrogen 1. e. to increase the yield.
Further I have found that to obtain acetylene one is not obliged to prepare it only from methane. One can obtain it from all other gaseous or gasifled hydrocarbons, mixtures of natural or synthetic hydrocarbons, and in general from any other organic material under the condition that it should first pass through the methane phase, with or without the addition of hydrogen.
I have shown by experiments that one condition which assists the transformation reaction of methane by preventing the dissociation of a part of the acetylene (i. e. by increasing its thermic stability) is to dilute these gases with other inert gases under the conditions under which the reaction takes place.
I claim:-
1. In the manufacture of acetylene, the process which comprises passing a gas, selected from a class consisting of methane and gases containing a substantial quantity of methane, into a reaction zone, maintained at temperatures ranging from about 1400 C. to 2000 C. and in the absence oi air, and exhausting the acetylene-containing reaction products from the reaction zone thereby producing a reduced pressure in said zone.
2. The process of claim 1 wherein the gas employed comprises methane diluted with an inert gas.
3. The process of claim 1 wherein the gas employed is diluted with hydrogen.
MARTIN BANCK.
Publications (1)
Publication Number | Publication Date |
---|---|
USRE19794E true USRE19794E (en) | 1935-12-24 |
Family
ID=2084202
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US19794D Expired USRE19794E (en) | Preparation of acetylene |
Country Status (1)
Country | Link |
---|---|
US (1) | USRE19794E (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2721227A (en) * | 1951-07-02 | 1955-10-18 | Stanolind Oil & Gas Co | Method and apparatus for making acetylene |
US6130260A (en) | 1998-11-25 | 2000-10-10 | The Texas A&M University Systems | Method for converting natural gas to liquid hydrocarbons |
US6602920B2 (en) | 1998-11-25 | 2003-08-05 | The Texas A&M University System | Method for converting natural gas to liquid hydrocarbons |
-
0
- US US19794D patent/USRE19794E/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2721227A (en) * | 1951-07-02 | 1955-10-18 | Stanolind Oil & Gas Co | Method and apparatus for making acetylene |
US6130260A (en) | 1998-11-25 | 2000-10-10 | The Texas A&M University Systems | Method for converting natural gas to liquid hydrocarbons |
US6602920B2 (en) | 1998-11-25 | 2003-08-05 | The Texas A&M University System | Method for converting natural gas to liquid hydrocarbons |
US7119240B2 (en) | 1998-11-25 | 2006-10-10 | The Texas A&M University System | Method for converting natural gas to olefins |
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