US1436550A - feance - Google Patents
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- US1436550A US1436550A US1436550DA US1436550A US 1436550 A US1436550 A US 1436550A US 1436550D A US1436550D A US 1436550DA US 1436550 A US1436550 A US 1436550A
- Authority
- US
- United States
- Prior art keywords
- acetylene
- mercury
- aldehyde
- kilos
- acetaldehyde
- 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
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- IKHGUXGNUITLKF-UHFFFAOYSA-N acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 72
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 64
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 56
- 229910052753 mercury Inorganic materials 0.000 description 42
- 238000000034 method Methods 0.000 description 38
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 36
- 229910000460 iron oxide Inorganic materials 0.000 description 34
- 239000000203 mixture Substances 0.000 description 32
- JEIPFZHSYJVQDO-UHFFFAOYSA-N Iron(III) oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 30
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 30
- 238000004519 manufacturing process Methods 0.000 description 26
- 239000001117 sulphuric acid Substances 0.000 description 26
- 235000011149 sulphuric acid Nutrition 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 229940008718 metallic mercury Drugs 0.000 description 24
- 238000006243 chemical reaction Methods 0.000 description 22
- 238000010521 absorption reaction Methods 0.000 description 20
- UKWHYYKOEPRTIC-UHFFFAOYSA-N Mercury(II) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 description 16
- 239000007800 oxidant agent Substances 0.000 description 16
- 239000002253 acid Substances 0.000 description 14
- 239000000126 substance Substances 0.000 description 14
- HSFWRNGVRCDJHI-UHFFFAOYSA-N acetylene Chemical compound C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 12
- 238000005755 formation reaction Methods 0.000 description 12
- 238000006116 polymerization reaction Methods 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 230000000887 hydrating Effects 0.000 description 8
- 230000036571 hydration Effects 0.000 description 8
- 238000006703 hydration reaction Methods 0.000 description 8
- 229940101209 mercuric oxide Drugs 0.000 description 8
- 239000011269 tar Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 230000000875 corresponding Effects 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 150000002730 mercury Chemical class 0.000 description 6
- 230000001590 oxidative Effects 0.000 description 6
- CWYNVVGOOAEACU-UHFFFAOYSA-N fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- -1 mercury aldehyde Chemical class 0.000 description 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 4
- 230000001603 reducing Effects 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 241000896693 Disa Species 0.000 description 2
- 241000286904 Leptothecata Species 0.000 description 2
- LWJROJCJINYWOX-UHFFFAOYSA-L Mercury(II) chloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 2
- 240000001987 Pyrus communis Species 0.000 description 2
- 235000014443 Pyrus communis Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000003197 catalytic Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000001627 detrimental Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000011872 intimate mixture Substances 0.000 description 2
- 229960002523 mercuric chloride Drugs 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000003638 reducing agent Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/26—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydration of carbon-to-carbon triple bonds
-
- 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
- B01J38/00—Regeneration or reactivation of catalysts, in general
Definitions
- LAURENT EMILE MARIE TREVOUX OF PETIT-QUEVILLY, FRANCE, ASSIGNOR TO LA SOCIETE ANONYME DE PRODUITS CHIMIQUES (ETABLISSEMENTS MALETRA), OF
- the amount of aldehyde produced varies greatly, according to the way in which the operation is performed.
- the mercury salt used as catalyzer is gradually reduced and at the end of a certain time is entirely transformed into a greyish powder. At this point the reaction stops, and the formation of aldehyde ceases.
- the quantity of aldehyde produced would, therefore, appear to depend essentially on the. speed with which the reduction of the mercury salt is, effected.
- the object of the present invention is a process for the production of acetaldehyde which enables the obtaining of much larger, and practically unlimited amounts of this aldehyde from a given weight of mercury.
- the essential characteristic of this process consists in using, as catalyzer, metallic mercury to which has been added an oxidizing Application filed March 24, 1920. Serial No. 368,348.
- the catalyzer consists solely of mercury either in the state of metallic mercury or in the form of reduced mercury, no
- the combination of the acetylene with water is effected by adding an oxidizing agent such as ferric oxide, and acetaldehyde can be prepared in unlimited quantities,
- the mercury can therefore be used indefinitely as catalyzer, all that is necessary beall that is necessary being that the oxidizing power of the substance used should be sufficient to maintain the catalytic action of the catalyzer and that it should'decompose the intermediate compound of mercury aldehyde formed, but not oxidize the aldehyde.
- the catalyzer may be prepared in the following manner:
- aldehyde compound is immediately formed and the aldehyde vapors are directly condensed in suitable refrigerating means.
- the cata yzer of the present invention which consists of metallic mercury and an added oxidizing agent such as ferric oxide may exhibit the maximum activ'ity, a number of conditions require to be fulfilled.
- the quantity of sulphuric acid used '1s preferably to of the mixture. With this proportion, coupled with a suitable temperature and a suitable flow of acetylene, an almost theoretical yield of pure aldehyde is obtained. An excessive sulphuric acid content leads to the formation of polymerization. products of aldehyde, (aldols, crotonaldehydes, tars). Similarly, an excessive rate 'of flow of the acetylene is detrimental to the satisfactory progress of the reaction, which being exothermic requires a certain equilib rium of temperature to be maintained. The purity of the gas also plays an essential part in the progress of the reaction.
- the yield of aldehyde may vary considerably with the extent to which the impurities, especially phosphoretted hydrogen, in the gas have been removed.
- the gas after being washed with a purifying agent containing metallic oxichlorides may be advantion of the catalyzer throughout the course tageously passed through a column containing a hydrochloric solution of mercuric chloride which is a very sensitive re-agent, for hydrogen phosphide.
- the temperature of the reaction must be between and 83 C. Below 70 C. the absorption is slower, whilst above 83 C.-'polymerization begins and the residue after the operation contains a considerable amount of tars. 4
- the water necessary for the hydration of the acetylene is added'periodically at certain intervals in a quantity corresponding to the Weight of aldehyde formed during such intervals.
- Sulphuric acid may be replaced by 'another suitable acid such as a sulphonic acid, or part of the sulphuric acid may be replaced by a fatty acid, such as acetic acid which is a good solvent for acetylene.
- the essential advantage of the process is that the mercury employed as catalyzer can be used indefinitely.
- the mercury employed as catalyzer can be used indefinitely.
- the mercury is reduced it has to be regenerated, an operation which is very expensive and is entirely dispensed with in the present invention.
- the only substance which is periodically and systematically renewed is the ferric oxide, a substance which costs little, and can be easily separated from the mercury as soon as it is reduced to the ferrous state; whilst the mercury plays the part of a continuous catalyst.
- the catalyzer used is mercury in the metallic or in the reduced state.
- either mercuric oxide, in acid solution, or a mercuric salt, may take the place of the initial charge of mercury.
- this operation may be repeated almost to an unlimited extent by periodically renewing the acid ferric oxide solution.
- the absorption liquor should contain a small amount of tars, these latter are separated from the mercurial catalyzer, which is used again.
- a commencement is made with the reduced mercury obtained by the reduction of 10 kilos of mercuric oxide.
- This oxide may be reduced by means of a suitable organic reducing agent such as formaldehyde, acetaldehyde, sugar or the like.
- a suitable organic reducing agent such as formaldehyde, acetaldehyde, sugar or the like.
- 10 kilos of mercuric oxide 13.34 kilos of 100% sulphuric acid and 191 kilos of water, 200 to 210 kilos of aldehyde are obtained.
- the liquid is decanted and 7.4 kilos of ferric oxide, 70 kilos of sulphuric acid and 191 kilos of water are added to the reduced mercury.
- the operation is then continued in the same way as in Examp e 1.
- a process for the production of acetaldehyde from acetylene comprising hydrating acetylene in t e presence of a catalyzer consisting of a mixture of metallic mercury, a sulfur acid and an oxidizing agent capable of maintaining the catalyzing action of the mercury indefinitely; substantially as described.
- a process for the production of acetaldehyde from acetylene comprising hydratlng acetylene in the presence of a catalyzer consisting of a mixture of metallic mercury, a sulfur acid and ferric oxide; substantially as described.
- a process for the production of acetaldehyde from acetylene comprising hydrating acetylene in the presence of a catalyzer conslsting of a mixture of metallic mercury and an oxidizing agent capable of maintaining the catalyzing action of the mercury indefinitely, and adding concentrated sulphuric acid to obtain a theoretic yield of pure aldehyde and to avoid the formation of polymerization products of aldehyde; substantially as described.
- a process for the production of acetal dehyde from acetylene comprising hydrating acetylene in the presence of a catalyzer consisting of a mixture of metallic mercury and ferric oxide, and adding concentrated sulphuric acid to obtain a theoretic yield of pure aldehyde and to avoid the formation of polymerization products of aldehyde; substantially as described.
- a process for the production of acetaldehyde from acetylene comprising passing an excess of acetylene gas'in contact with an agitated mixture of metallic mercury and an oxidizing agent capable of maintaining the catalyzing action of the mercy indefinitely and containing concentrated sulphuric acid, maintaining the temperature of the mixture at between 70 and 83 0., and adding the Water necessary for the hydration of the acetylene at intervals cor responding to the weight of acetaldehyde formed during such intervals; substantially as described.
- a process for the production of acetaldehyde from acetylene comprising passing an excess of acetylene gas in contact with an agitated mixture of metallic mercury and ferric oxide, maintaining the temperature of the mixture at between 70 and 83 C., and adding the water necessary for the hydration of the acetylene at intervals corresponding to the weight of acetaldehyde formed during such intervals; substantially as described.
- a process for the production of acetaldehyde from acetylene comprising passing an excess of acetylene gas in contact with an agitated mixture of metallic mercury and concentrated sulphuric acid and water, maintaining the temperature of the mixture at between 70 and 80 C., and gradually adding an oxidizing agent capable of maintaining the catalyzing action of the mercury indefinitely, at certain intervals and at the rate at which the the oxidizing agent is reduced.
- a process for the production of acetaldehyde from acetylene comprising pass ng an excess of acetylene gas in contact with an agitated mixture of metallic mercury and concentrated sulphuric acid and water, mamtaining the temperature of the mixture at between 70 and 80 C., and gradually adding ferric oxide to the mixture, so as to maintain the catalyzing action of the mercury indefinitely, at certain intervals and at the rate at which ferrous oxide is formed.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Description
Patented Nov. 21, 1922.
LAURENT EMILE MARIE TREVOUX, OF PETIT-QUEVILLY, FRANCE, ASSIGNOR TO LA SOCIETE ANONYME DE PRODUITS CHIMIQUES (ETABLISSEMENTS MALETRA), OF
PETIT-QUEVILLY, FRANCE.
PROCESS FOR THE PRODUCTION OF ACETALDEHYDE FROM ACETYLENE.
No Drawing.
To all whom it may concern:
Be it known that I, LAURENT EMILE MARIE Tnsvoux, citizen ofthe Republic of France, and resident of Petit-Quevilly, Seine Inferieure (post-oilice address 143 Route de Caen), France, have invented a new and useful Process for the Production of Acct-aldehyde from Acetylene, which improvements are fully set forth in the following specification.
A number of patents and processes exist for the production of acetaldehyde from acetylene, all of them based on the same re action, namely, the combining of acetylene with water by means of a catalyzing agent, a mercury saltgenerally in an acid medium. The only difference between these processes is with regard to the kind of mercury salt used, the nature and concentration of the acid, the temperature of reaction and the rate of supply of the acetylene gas.
The amount of aldehyde produced varies greatly, according to the way in which the operation is performed. The mercury salt used as catalyzer is gradually reduced and at the end of a certain time is entirely transformed into a greyish powder. At this point the reaction stops, and the formation of aldehyde ceases. The quantity of aldehyde produced would, therefore, appear to depend essentially on the. speed with which the reduction of the mercury salt is, effected.
In order to lower the cost of manufacturing the aldehyde, it is desirable to produce 20 times that weight.
v. The object of the present invention is a process for the production of acetaldehyde which enables the obtaining of much larger, and practically unlimited amounts of this aldehyde from a given weight of mercury.
The essential characteristic of this process consists in using, as catalyzer, metallic mercury to which has been added an oxidizing Application filed March 24, 1920. Serial No. 368,348.
substance adapted to impart to the mercury a special activity which enables it to form the mercury-aldehyde compound in a. stable condition, and maintain the catalyzing action of the contact substance indefinitely. If the catalyzer consists solely of mercury either in the state of metallic mercury or in the form of reduced mercury, no
absorption of the acetylene takes place.
The combination of the acetylene with water is effected by adding an oxidizing agent such as ferric oxide, and acetaldehyde can be prepared in unlimited quantities,
provided that a certain proportion of ferric oxide is maintained in the absorption liquor. The reaction does not stop until the added agent has lost its oxidizing power.
The mercury can therefore be used indefinitely as catalyzer, all that is necessary beall that is necessary being that the oxidizing power of the substance used should be sufficient to maintain the catalytic action of the catalyzer and that it should'decompose the intermediate compound of mercury aldehyde formed, but not oxidize the aldehyde.
lVith oxidizing agents that are too energetic, or with a substance capable of liberating oxygen in the nascent state, a negative result would be obtained, and the formation of aldehyde would be arrested.
In the present invention the catalyzer may be prepared in the following manner:
An intimate mixture of reduced mercury and of ferric oxide is prepared, the necessary acid and water for hydrating the acetylene being then added. If an excess of purified acetylene is introduced at a temperature of 80 C., and under suitable pressure, into the absorption apparatus, which is provided with a mechanical stirrer, the reaction begins, the
aldehyde compound is immediately formed and the aldehyde vapors are directly condensed in suitable refrigerating means.
The absorption of the acetylene proceeds in a very regular manner, and only ceases we when the ferric oxide has' been completely I transformed into ferrous oxide. If the v.
sorption liquid are added. The presence of a few globules of mercury in the liquid does not interfere with the reaction, as the mechanical agitation in the course of the reaction causes them to disa pear.
In order that the cata yzer of the present invention which consists of metallic mercury and an added oxidizing agent such as ferric oxide may exhibit the maximum activ'ity, a number of conditions require to be fulfilled.
The quantity of sulphuric acid used '1s preferably to of the mixture. With this proportion, coupled with a suitable temperature and a suitable flow of acetylene, an almost theoretical yield of pure aldehyde is obtained. An excessive sulphuric acid content leads to the formation of polymerization. products of aldehyde, (aldols, crotonaldehydes, tars). Similarly, an excessive rate 'of flow of the acetylene is detrimental to the satisfactory progress of the reaction, which being exothermic requires a certain equilib rium of temperature to be maintained. The purity of the gas also plays an essential part in the progress of the reaction. It has been found that the yield of aldehyde may vary considerably with the extent to which the impurities, especially phosphoretted hydrogen, in the gas have been removed. In order to be able to check at any moment the degree of purity of the gas, the gas after being washed with a purifying agent containing metallic oxichlorides, may be advantion of the catalyzer throughout the course tageously passed through a column containing a hydrochloric solution of mercuric chloride which is a very sensitive re-agent, for hydrogen phosphide.
Finally, the temperature of the reaction must be between and 83 C. Below 70 C. the absorption is slower, whilst above 83 C.-'polymerization begins and the residue after the operation contains a considerable amount of tars. 4
In order to maintain the same concentr of the process, the water necessary for the hydration of the acetylene is added'periodically at certain intervals in a quantity corresponding to the Weight of aldehyde formed during such intervals.
As in similar processes, energetic mechanical agitation is required in the absorption apparatus in order to mix the acetylene intimately with the contact substance.
Sulphuric acid may be replaced by 'another suitable acid such as a sulphonic acid, or part of the sulphuric acid may be replaced by a fatty acid, such as acetic acid which is a good solvent for acetylene.
With such an acid the reaction is much quicker and the absorption is intensified, so that it is more difiicult to avoid polymerization and the formation of tars.
The essential advantage of the process is that the mercury employed as catalyzer can be used indefinitely. In all the other processes, on the contrary, as soon as the mercury is reduced it has to be regenerated, an operation which is very expensive and is entirely dispensed with in the present invention. In the present process, the only substance which is periodically and systematically renewed is the ferric oxide, a substance which costs little, and can be easily separated from the mercury as soon as it is reduced to the ferrous state; whilst the mercury plays the part of a continuous catalyst.
As can be seen from the above the catalyzer used is mercury in the metallic or in the reduced state. However, without departing from the scope of the invention either mercuric oxide, in acid solution, or a mercuric salt, may take the place of the initial charge of mercury.
E wample In a suitable agitation apparatus 9.26 kilos of metallic mercury are triturated with 7.4 kilos of ferric oxide, 70 kilos of 100% sulphuric acid, and 191 kilos of water are added and the mixture is heated to 80 C. Thereupon, a suitable excess of acetylene is introduced under the necessary pressure, the temperature being maintained between 70 and 83 C. preferably at 80 during the reaction. The amount of water required for hydration, which corresponds to the weight of aldehyde obtained, 'is added at certain intervals so as to maintain a suitable content of water in the absorption liquor throughout.
In this way 280 kilos of acetic aldehyde are obtained.
As soon as all the ferric salt has been transformed into the ferrous state, 7 .4 more kilos of ferric oxide and 13.34 kilos of sulphuric acid are added to the absorption liquor. By continuing to work under the same conditions as described above, 280 more kilos of acetaldehyde are obtained.
Theoretically, this operation may be repeated almost to an unlimited extent by periodically renewing the acid ferric oxide solution.
If after a certain number of operations the absorption liquor should contain a small amount of tars, these latter are separated from the mercurial catalyzer, which is used again.
E wample 2.
A commencement is made with the reduced mercury obtained by the reduction of 10 kilos of mercuric oxide. This oxide may be reduced by means of a suitable organic reducing agent such as formaldehyde, acetaldehyde, sugar or the like. In this Way by using 10 kilos of mercuric oxide, 13.34 kilos of 100% sulphuric acid and 191 kilos of water, 200 to 210 kilos of aldehyde are obtained. At this point all the mercuric oxide will have been reduced. The liquid is decanted and 7.4 kilos of ferric oxide, 70 kilos of sulphuric acid and 191 kilos of water are added to the reduced mercury. The operation is then continued in the same way as in Examp e 1.
By this means 280 kilos of acetaldehyde are obtained.
By renewing the ferric oxide at every operation a fresh quantity of 280 kilos of acetaldeh de is obtained in each case.
What claim as new and desire to secure by Letters Patent of the United States is 1. A process for the production of acetaldehyde from acetylene, comprising hydrating acetylene in t e presence of a catalyzer consisting of a mixture of metallic mercury, a sulfur acid and an oxidizing agent capable of maintaining the catalyzing action of the mercury indefinitely; substantially as described.
2. A process for the production of acetaldehyde from acetylene, comprising hydratlng acetylene in the presence of a catalyzer consisting of a mixture of metallic mercury, a sulfur acid and ferric oxide; substantially as described.
3. A process for the production of acetaldehyde from acetylene, comprising hydrating acetylene in the presence of a catalyzer conslsting of a mixture of metallic mercury and an oxidizing agent capable of maintaining the catalyzing action of the mercury indefinitely, and adding concentrated sulphuric acid to obtain a theoretic yield of pure aldehyde and to avoid the formation of polymerization products of aldehyde; substantially as described.
4. A process for the production of acetal dehyde from acetylene, comprising hydrating acetylene in the presence of a catalyzer consisting of a mixture of metallic mercury and ferric oxide, and adding concentrated sulphuric acid to obtain a theoretic yield of pure aldehyde and to avoid the formation of polymerization products of aldehyde; substantially as described.
5. A process for the production of acetaldehyde from acetylene, comprising passing an excess of acetylene gas'in contact with an agitated mixture of metallic mercury and an oxidizing agent capable of maintaining the catalyzing action of the mercy indefinitely and containing concentrated sulphuric acid, maintaining the temperature of the mixture at between 70 and 83 0., and adding the Water necessary for the hydration of the acetylene at intervals cor responding to the weight of acetaldehyde formed during such intervals; substantially as described.
6. A process for the production of acetaldehyde from acetylene, comprising passing an excess of acetylene gas in contact with an agitated mixture of metallic mercury and ferric oxide, maintaining the temperature of the mixture at between 70 and 83 C., and adding the water necessary for the hydration of the acetylene at intervals corresponding to the weight of acetaldehyde formed during such intervals; substantially as described.
7. A process for the production of acetaldehyde from acetylene, comprising passing an excess of acetylene gas in contact with an agitated mixture of metallic mercury and concentrated sulphuric acid and water, maintaining the temperature of the mixture at between 70 and 80 C., and gradually adding an oxidizing agent capable of maintaining the catalyzing action of the mercury indefinitely, at certain intervals and at the rate at which the the oxidizing agent is reduced.
8. A process for the production of acetaldehyde from acetylene, comprising pass ng an excess of acetylene gas in contact with an agitated mixture of metallic mercury and concentrated sulphuric acid and water, mamtaining the temperature of the mixture at between 70 and 80 C., and gradually adding ferric oxide to the mixture, so as to maintain the catalyzing action of the mercury indefinitely, at certain intervals and at the rate at which ferrous oxide is formed.
Witness ALPHONSE NICOLAS.
Publications (1)
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US1436550A true US1436550A (en) | 1922-11-21 |
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US1436550D Expired - Lifetime US1436550A (en) | feance |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3281476A (en) * | 1966-10-25 | Dae-tmp | ||
US3458591A (en) * | 1967-12-04 | 1969-07-29 | Firestone Tire & Rubber Co | Removal of alkyne impurity from butadiene-1,2 |
-
0
- US US1436550D patent/US1436550A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3281476A (en) * | 1966-10-25 | Dae-tmp | ||
US3458591A (en) * | 1967-12-04 | 1969-07-29 | Firestone Tire & Rubber Co | Removal of alkyne impurity from butadiene-1,2 |
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