US1868127A - Production of valuable hydrocarbons - Google Patents
Production of valuable hydrocarbons Download PDFInfo
- Publication number
- US1868127A US1868127A US328849A US32884928A US1868127A US 1868127 A US1868127 A US 1868127A US 328849 A US328849 A US 328849A US 32884928 A US32884928 A US 32884928A US 1868127 A US1868127 A US 1868127A
- Authority
- US
- United States
- Prior art keywords
- carbon
- acetylene
- mixture
- production
- metals
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229930195733 hydrocarbon Natural products 0.000 title description 13
- 150000002430 hydrocarbons Chemical class 0.000 title description 13
- 238000004519 manufacturing process Methods 0.000 title description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 21
- 229910052799 carbon Inorganic materials 0.000 description 20
- 239000000203 mixture Substances 0.000 description 20
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 19
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 19
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- 150000002739 metals Chemical class 0.000 description 14
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 13
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 13
- 239000011135 tin Substances 0.000 description 13
- 229910052718 tin Inorganic materials 0.000 description 13
- 229910052725 zinc Inorganic materials 0.000 description 13
- 239000011701 zinc Substances 0.000 description 13
- 229910045601 alloy Inorganic materials 0.000 description 12
- 239000000956 alloy Substances 0.000 description 12
- 229910052782 aluminium Inorganic materials 0.000 description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 239000011133 lead Substances 0.000 description 11
- 239000004411 aluminium Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 229910052710 silicon Inorganic materials 0.000 description 10
- 239000010703 silicon Substances 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
- 239000005977 Ethylene Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 230000008021 deposition Effects 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- HPDFFVBPXCTEDN-UHFFFAOYSA-N copper manganese Chemical compound [Mn].[Cu] HPDFFVBPXCTEDN-UHFFFAOYSA-N 0.000 description 2
- 230000003292 diminished effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000003921 oil Substances 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
- 230000000630 rising effect Effects 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000011269 tar Substances 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 241000792765 Minous Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- LQJIDIOGYJAQMF-UHFFFAOYSA-N lambda2-silanylidenetin Chemical compound [Si].[Sn] LQJIDIOGYJAQMF-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229910001510 metal chloride Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver 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
-
- 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
- B01J19/0006—Controlling or regulating processes
- B01J19/002—Avoiding undesirable reactions or side-effects, e.g. avoiding explosions, or improving the yield by suppressing side-reactions
- B01J19/0026—Avoiding carbon deposits
Definitions
- This invention relates to improvements in the manufacture and production of valuable hydrocarbons, especially those of liquid nature, althou h the production of gaseous hydrocarbons, ior example diolefines, such as bllitadiene or its homologues is also contemp ated. t
- hydrocarbons of higher molecular weight than that of the initial material can be produced by heating mixtures comprisin olefines and acetylene; for example, it is own-that, inter alia, butadiene can be obtained by heating a mixture of ethylene and acetylene in a lass retort to such a temperature that the said retort is brought to redness.
- butadiene can be obtained by heating a mixture of ethylene and acetylene in a lass retort to such a temperature that the said retort is brought to redness.
- glass, quartz, porcelain, iron, nickel, copper, silver and many other materials suitable for the apparatus used in this reaction cause extensive deposition of carbon and for this reason it has not hitherto been possible to carry out the processon a technical scale, because this is only practicable when the deposition of carbon is prevented.
- the process may be carried on under elevated, atmospheric or diminished pressure. Usually pressure of up to about 50 or '100 atmospheres are employed, but, if desired,
- reaction is usually carried out between about. 200 and 800 C. and preferably between about 300 and 600 C.
- reaction chamber for example, on plates, in the reaction chamber.
- the operation may be carried on in the presence of catalytic substances having a condensing action other than those hereinbefore specified.
- Anhydrous chlorides of the heavy metals such as v "be in excess, and, if desired, the mixture may be diluted with one or more extraneous gases, or example nitrogen, methane or ethane, carbon dioxide or carbon monoxide.
- the latter method of operating may also be carried on under elevated or diminished pressure.
- Example '1 v A mixture of equal parts of ethylene and acetylene is passed, from above downwards,
- Example 2 370 to 400 C., the reaction commences whereupon the same temperature is maintained for about 6 hours. On cooling, 72 per cent by weight of the mixture of ethylene and acetylene employed is recovered in the form of oil, of which 10 per cent, consisting mainly of butylene, boils below ordinary temperature, per cent, consisting mainly of benzene and toluene, boils up to 120 (1, and the rest boils up to 150 C. The catalyst remains perfectly free from tar or carbon.
- Example 3 A mixture of 9 parts of ethylene and 1 part of acetylene is passed, at the rate of 10 liters per hour, through a manganese-copper tube coated internally with tin, 18 millimeters in diameter, which is heated over a length of 60' centimeters to about 600 C. 4' per cent of the transmitted gases is continuously converted, and the tube does not show the slightest deposition of carbon, even after prolonged use.
- the condensate obtained on cooling to low temperatures contains 13 per cent of butadione, which'can be readily identified in the form of tetrabromide by adding on bromine. A further 7 per cent of the converted materials boils'below ordinary temperatures and the remainder boils up to about C.
- the residual gas contains ethylene, acetylene, a little propylene and butylene, and also 0.5 be employed for the process again after the addition of acetylene, which is the chief constituent consumed.
- Example 3 The same conversion as described in Example 3 is carried on in a manganese copper tube coated internally with zinc. 5.5 per cent of the gas is converted into a liquid which boils, for the most part at between about 60 C. and 80 0., and consists almost entirely of benzene. Merely traces of buta diene can be detected in the conversion mixture, and only traces of methane are. present in the residual gas. No deposit of carbon can be found in the-tube itself after being in use for 120 hours. Benzene is also obtained as the chief product by-operating, in a similar way, at about 600 C., with a brass tube.
- the tube may be replaced, for example, by an electrically heated tinned radiator of copper wire.
- the operation may 60 per cent carbons by heating a lead, tin, zinc,
- Tin, zinc and the like have also proved very advantageous for internally coating the apparatus, in cases, where gases obtained b pyrogenic decomposition of tars, oils, b minous coals and the like and which contain olefines and acetylene, for example, 20-to 40 the ituper cent of the former and about 1 to 2 per cent of the latter, are subjected to the aforesaid treatment, since the said metals prevent the deposition of carbon.
- 2- 1 In the production of valuable hydroolefine and acetylene, the step of brmgmg the said initial materials, while in the hot state, only into contact with substances selected from the class consisting .of carbon, silicon,
- aluminium and alloys containfine and acetylene, the step 0 bringing the y said initial materials, while in the hot state, only into contact with substances selec from the class consisting of carbon, silicon, aluminium and ing-substantial amounts of these metals, and maintaining an elevated pressure.
- the step 0 bringing the said initial materials, while in the hot state, only into contact with substances se-' lected from the class consisting of carbon, silicon, lead, tin, zinc, aluminium and alloys containing substantial amounts of in dilution with an extraneous as.
- vauable hydro-' from the class consisting of carbon, silicon,
- alloys containthese metals, andemploying the initial m xture:
- step 0 bringing the said initial materials, while in the hot state, only into contact with substances selected from the class consisting of carbon, silicon,
- a process for the production ofvaluable hydrocarbons which comprises passing a mixture comprismg ethylene and acet lene through a tube coated internally wit tin and heatedto about 600 C.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Description
Patented July 19, 1932 UNITED STATES PATENT; OFFICE;
rmz am) we EAEUBEB, or LnnwIosnArnN-oN-rnn-nnm, Gunman?) ABBIGNORS -TO I. G. FABBENINDUSTRIE AKTIENGESELLSCHAFT, OF FRANKFURT- ON-m-m, GERMANY, A CORPORATION OF GERMANY PRODUCTION OF V ALUAIBLE HYDROCARBONS Io Drawing. Application filed December 87, 1928, Serial No. 328,849, and in Germany January .5, 1888.
This invention relates to improvements in the manufacture and production of valuable hydrocarbons, especially those of liquid nature, althou h the production of gaseous hydrocarbons, ior example diolefines, such as bllitadiene or its homologues is also contemp ated. t
It is already known that hydrocarbons of higher molecular weight than that of the initial material can be produced by heating mixtures comprisin olefines and acetylene; for example, it is own-that, inter alia, butadiene can be obtained by heating a mixture of ethylene and acetylene in a lass retort to such a temperature that the said retort is brought to redness. But glass, quartz, porcelain, iron, nickel, copper, silver and many other materials suitable for the apparatus used in this reaction, cause extensive deposition of carbon and for this reason it has not hitherto been possible to carry out the processon a technical scale, because this is only practicable when the deposition of carbon is prevented.
We have now found that the said conversion ofolefines, such as ethyleneor propylene f together with acetylene can be carried out at high temperatures and without deposition of carbon if care be taken that the heated sees and vapors come into contact only with ree elements of grou 4 of the periodic system, such, for examp e, as tin silicon, lead,-
carbon in the form of graphite, or with zinc or aluminium or alloys containing substantial amounts of these metals. With this object in view it is essential that such hot portions of the conversion apparatus as come into contact with the gases and vapors should be constructed of the said metals or alloys or should be coated with them. The operation can also be conducted by simply passing the mixtures of olefines and acetylene under treatment through a highly heated bath of molten tin, zinc, lead, aluminium, or alloys of these metals with one another or withother metals which do not cause deposition of carbon, or with silicon or graphitic carbon.
The process may be carried on under elevated, atmospheric or diminished pressure. Usually pressure of up to about 50 or '100 atmospheres are employed, but, if desired,
higher pressures, for example 200 atmospheres or more, may also be employed. The reaction is usually carried out between about. 200 and 800 C. and preferably between about 300 and 600 C.
The materials hereinbefore specified not only prevent the deposition of carbon, but
also to a large extent exert a catalytic action. It is therefore advantageous to dispose them,
for example, on plates, in the reaction chamber.
It has also been found that the operation may be carried on in the presence of catalytic substances having a condensing action other than those hereinbefore specified. Anhydrous chlorides of the heavy metals, such as v "be in excess, and, if desired, the mixture may be diluted with one or more extraneous gases, or example nitrogen, methane or ethane, carbon dioxide or carbon monoxide. I
The latter method of operating may also be carried on under elevated or diminished pressure.
The following examples will further illustrate the nature of the saidinvention, but the invention is not restricted to these examples. The parts are by weight.
Example '1 v A mixture of equal parts of ethylene and acetylene is passed, from above downwards,
' per cent of methane. It can manganese also be conducted under elevated pressure.
Example 2 370 to 400 C., the reaction commences whereupon the same temperature is maintained for about 6 hours. On cooling, 72 per cent by weight of the mixture of ethylene and acetylene employed is recovered in the form of oil, of which 10 per cent, consisting mainly of butylene, boils below ordinary temperature, per cent, consisting mainly of benzene and toluene, boils up to 120 (1, and the rest boils up to 150 C. The catalyst remains perfectly free from tar or carbon.
Example 3 A mixture of 9 parts of ethylene and 1 part of acetylene is passed, at the rate of 10 liters per hour, through a manganese-copper tube coated internally with tin, 18 millimeters in diameter, which is heated over a length of 60' centimeters to about 600 C. 4' per cent of the transmitted gases is continuously converted, and the tube does not show the slightest deposition of carbon, even after prolonged use.
The condensate obtained on cooling to low temperatures contains 13 per cent of butadione, which'can be readily identified in the form of tetrabromide by adding on bromine. A further 7 per cent of the converted materials boils'below ordinary temperatures and the remainder boils up to about C. The residual gas contains ethylene, acetylene, a little propylene and butylene, and also 0.5 be employed for the process again after the addition of acetylene, which is the chief constituent consumed.
E'wample J;
The same conversion as described in Example 3 is carried on in a manganese copper tube coated internally with zinc. 5.5 per cent of the gas is converted into a liquid which boils, for the most part at between about 60 C. and 80 0., and consists almost entirely of benzene. Merely traces of buta diene can be detected in the conversion mixture, and only traces of methane are. present in the residual gas. No deposit of carbon can be found in the-tube itself after being in use for 120 hours. Benzene is also obtained as the chief product by-operating, in a similar way, at about 600 C., with a brass tube.
The tube may be replaced, for example, by an electrically heated tinned radiator of copper wire. The operation may 60 per cent carbons by heating a lead, tin, zinc,
Tin, zinc and the like have also proved very advantageous for internally coating the apparatus, in cases, where gases obtained b pyrogenic decomposition of tars, oils, b minous coals and the like and which contain olefines and acetylene, for example, 20-to 40 the ituper cent of the former and about 1 to 2 per cent of the latter, are subjected to the aforesaid treatment, since the said metals prevent the deposition of carbon. What we claim is 2- 1. In the production of valuable hydroolefine and acetylene, the step of brmgmg the said initial materials, while in the hot state, only into contact with substances selected from the class consisting .of carbon, silicon,
lead, tin, zinc, aluminium and alloys containing substantial amounts of these metals.
2. In theproduction of valuable hydrocarbons b heating a mixture comprising an olefine an acetylene, the step of bringing the said initial materials, only into contact with substances selected from theclass consisting of carbon, silicon, lead, tin, zinc, aluminium and alloys containing substantial amounts of these metals, and
- maintaining a temperature of between about 200 and 800 C.
3. In the production of valuable hydrocarbons by heating a mixture comprising an olefine and acetylene, the step of bringing the said initial materials while in the hot state,
only into contact with substances selectedfrom the class consisting of carbon, silicon,
lead, tin, zinc, ing substantial amounts of these metals, and maintaining a, temperature of between about 300and 600 C.
4. In the production of valuable hydrocarbons by heating a mixture com rising an olemixture comprising an while in the hot state,
aluminium and alloys containfine and acetylene, the step 0 bringing the y said initial materials, while in the hot state, only into contact with substances selec from the class consisting of carbon, silicon, aluminium and ing-substantial amounts of these metals, and maintaining an elevated pressure.
5. In thevproduction of valuable hydrocarbons by heating a mixture com risingan olefine and acetylene, the step 0 bringing the said initial materials, while in the hot state, only into contact with substances se-' lected from the class consisting of carbon, silicon, lead, tin, zinc, aluminium and alloys containing substantial amounts of in dilution with an extraneous as.
6. In the production of vauable hydro-' from the class consisting of carbon, silicon,
.lead, tin, zinc, aluminium and alloys containno. alloys containthese metals, andemploying the initial m xture:
ing substantial amounts of these metals, and treating the said mixture with a catalyst comprising an anhydrous'metal chloride.
7. In the production of valuable hydrocarbons by heating a mixture com rising an olefine and acetylene, the step 0 bringing the said initial materials, while in the hot state, only into contact with substances selected from the class consisting of carbon, silicon,
lead, tin, zinc, aluminum and alloys containing substantial amounts of these metals, and treating the said mixture with a catalyst comprising aluminum chloride.
8. In the production of valuable hydrocarbons by heating a mixture comprising an olefine and acetylene, the step of bringing a mixture comprising ethylene and acetylene, while in the hot state, only into contact with substances selected from the class consisting of carbon, silicon, lead, tin, zinc, aluminium and alloys containing substantial amounts of these metals.
9. In the production of valuable hydrocarbons by heatin a mixture comprising an olefine and acety ene, the step of bringing a mixture comprising ethylene and acetylene, while in the hot state, only into contact with substances selected from the class consisting of carbon, silicon, lead, tin, zinc, aluminium and alloys containing substantial amounts of these metals, and malntaining a temperature of between about 300 and 600 C.
10. A process for the production ofvaluable hydrocarbons which comprises passing a mixture comprismg ethylene and acet lene through a tube coated internally wit tin and heatedto about 600 C.
In testimony whereof we have hereunto set our hands. V
FRITZ WINKLER. HANS HA EUBER.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1868127X | 1928-01-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1868127A true US1868127A (en) | 1932-07-19 |
Family
ID=7746812
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US328849A Expired - Lifetime US1868127A (en) | 1928-01-05 | 1928-12-27 | Production of valuable hydrocarbons |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1868127A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2417119A (en) * | 1942-12-03 | 1947-03-11 | Gen Motors Corp | Synthesis of olefins by reacting an olefin with an alkyl halide in the presence of calcium oxide |
| US3247276A (en) * | 1962-07-09 | 1966-04-19 | Texaco Inc | Catalytic treatment of hydrocarbons |
| US3444253A (en) * | 1967-09-20 | 1969-05-13 | Union Carbide Corp | Addition reactions of butadiene catalyzed by copper (i) zeolites |
| US3513209A (en) * | 1968-08-19 | 1970-05-19 | Du Pont | Method of making 1,4-cyclohexadiene |
| US3527827A (en) * | 1968-10-25 | 1970-09-08 | Universal Oil Prod Co | Synthesis of monocyclic terpenes |
| EP0092959A3 (en) * | 1982-04-23 | 1984-03-28 | Exxon Research And Engineering Company | A method of coating a metal substrate with a protective aluminium-silicon coating, a metal substrate having the coating, and the use of the coated metal substrate |
| JP2008537737A (en) * | 2005-03-23 | 2008-09-25 | サウディ ベーシック インダストリーズ コーポレイション | Process for simultaneous production of benzene and ethylene by conversion of acetylene |
-
1928
- 1928-12-27 US US328849A patent/US1868127A/en not_active Expired - Lifetime
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2417119A (en) * | 1942-12-03 | 1947-03-11 | Gen Motors Corp | Synthesis of olefins by reacting an olefin with an alkyl halide in the presence of calcium oxide |
| US3247276A (en) * | 1962-07-09 | 1966-04-19 | Texaco Inc | Catalytic treatment of hydrocarbons |
| US3444253A (en) * | 1967-09-20 | 1969-05-13 | Union Carbide Corp | Addition reactions of butadiene catalyzed by copper (i) zeolites |
| US3513209A (en) * | 1968-08-19 | 1970-05-19 | Du Pont | Method of making 1,4-cyclohexadiene |
| US3527827A (en) * | 1968-10-25 | 1970-09-08 | Universal Oil Prod Co | Synthesis of monocyclic terpenes |
| EP0092959A3 (en) * | 1982-04-23 | 1984-03-28 | Exxon Research And Engineering Company | A method of coating a metal substrate with a protective aluminium-silicon coating, a metal substrate having the coating, and the use of the coated metal substrate |
| JP2008537737A (en) * | 2005-03-23 | 2008-09-25 | サウディ ベーシック インダストリーズ コーポレイション | Process for simultaneous production of benzene and ethylene by conversion of acetylene |
| US20090287031A1 (en) * | 2005-03-23 | 2009-11-19 | Agaddin Mamadov | Process for Simultaneous Production of Benzene and Ethylene by Conversion of Acetylene |
| US8013198B2 (en) | 2005-03-23 | 2011-09-06 | Saudi Basic Industries Corporation | Process for simultaneous production of benzene and ethylene by conversion of acetylene |
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