US690062A - Method of making sulfuric anhydrid. - Google Patents
Method of making sulfuric anhydrid. Download PDFInfo
- Publication number
- US690062A US690062A US12039A US1900012039A US690062A US 690062 A US690062 A US 690062A US 12039 A US12039 A US 12039A US 1900012039 A US1900012039 A US 1900012039A US 690062 A US690062 A US 690062A
- Authority
- US
- United States
- Prior art keywords
- reaction
- pipe
- contact
- making sulfuric
- sulfuric anhydrid
- 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
- 238000004519 manufacturing process Methods 0.000 title description 3
- 239000007789 gas Substances 0.000 description 11
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 102000004338 Transferrin Human genes 0.000 description 1
- 108090000901 Transferrin Proteins 0.000 description 1
- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 1
- QEVHRUUCFGRFIF-MDEJGZGSSA-N reserpine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C(C5=CC=C(OC)C=C5N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 QEVHRUUCFGRFIF-MDEJGZGSSA-N 0.000 description 1
- 239000012581 transferrin Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B17/00—Sulfur; Compounds thereof
- C01B17/69—Sulfur trioxide; Sulfuric acid
- C01B17/74—Preparation
- C01B17/76—Preparation by contact processes
- C01B17/765—Multi-stage SO3-conversion
Definitions
- Figure 1 is a Vertical section of an apparatus containing a single contact-chamber, represented by a tube or pipe R.
- Fig. 2 is a vertical section of an apparatus containing a pluralityof contactchambers, represented by tubes or pipes R.
- M represents a brickwork structure or an iron pipe.
- this pipe R is fixed, leaving the passage S' between.
- This pipe R consists of two parts co and b, which have different functions and may difer from one another in length and diameter. Also either part can be replaced by aplurality of narrower pipes.
- the portion b ot' the pipe R is occupied bythe contact substance, (indicated in the drawings by broken section lines,) and this is cooled by the cold air entering the passage S' at n.
- the other part a of the pipe R the gases containing the sulfur dioxid which enter at O are heated to the temperature necessary for the reaction.
- the whole apparatus is first raised to the temperature necessary for the reaction by heating by means of h 7-say gas-flames. Then, when gases rich in sulfur dioxid are used, after the reaction has once commenced further heating is unnecessary, because the air' as it passes through the pipe M in contact with that part b of the pipe R in which the reaction is in progress in extracting the eXcess of heat due to the reaction absorbs the heat and transfers sufficient heat to the other portion a to prevent a change of position of the reaction zone or the entire cessation of the reaction.
- the current of air can be regulated by means of the updraft-openings L L, which are adjustable by the' slides Z l.
- the contact substance in b is constantly maintained at the most favorable temperature for the reaction.
- the gases contain but little sulfur dioXid
- the air which is somewhat heated by its cooling' action on the contact substance, is further heated by suitable means h' h', (such as gas-flames,) so that the gases in flowing through part a receive a greater increment of heat.
- suitable means h' h' such as gas-flames,
- the gases are still poorer in sulfur dioxid, it may be necessary to continually heatto some eX- tent the current of air fiowing in through n, either by means of the gas-flames at h h or in some other way.
- the gases containing the sulf uric anhydrid issuing from the contact-chamber b leave the apparatus by the pipe O and are worked up in any suitable way.
- the apparatus represented in Fi g. 2 is made up of a plurality of contact-tubes R R, which are in connection with one another by means of the two tube-plates W W and the covers D D' above and below. In other respects it resembles Fig. 1.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Description
PatentedDec. 3l, !901.
B. KNIETSCH. METHOD OF MAKiNG SULFURIC ANHYDRID.
(Application filed Apr. 7. 1900.)
(No Model.)
D T A a R. Em
16 T M a haf h Urrnn reres ATENT OFFICE.
RUDOLF KNIETSOH, OF LUDYVIGSHAFEN, GERMANY, ASSIGNOR TO THE BADISCHE ANILIN 85 SODA FABRIK, OF LUDVVIGSHAFEN, GERMANY, A
CORPORATION OF GERMANY.
METHOD OF MAKING SULFURIC ANHYDRID.
SPECIFICATION forming part of Letters Patenta No. 690,062, dated December 31 1901.
Original application filed July 14, 1898, Serial No. 685369. Divide& and this application filed April '7, 1900. Serial No. 12,039. (No specimensl To all whom it may conccrn:
Be it known thatl, RUDOLF KNIETSCH, doctor of hilosophy, a subject of the King of Prussia,Enperorof Germany,residin g at Ludwigshafen-on-the-Rhine,Kingdom of Bavaria, Germany, have invented certain new and usef ul Improvements in the Process for the Manufacture of Sulfuric Anhydrids, (which inventionis divided outof myapplicationtorLetters Patent filed July let, 1898, Serial No. 685,969, which application had previously been divided, giving rise to the application filed August 18, 1899, Serial No. 727,63G,) of which the following is a specification.
In my application, Serial No. 681969, filed July 14:, 1898, I described the apparatus and process described in this application. In the application, Serial No. 727,(336, filed August 1899, I described aspecific form of apparatus and claimed the specific apparatus and the process as carried out therewith. I file the present application as a division of the said application for the purpose of securing the specific claim on the said process.
In the accompanying drawings, Figure 1 is a Vertical section of an apparatus containing a single contact-chamber, represented by a tube or pipe R. Fig. 2 is a vertical section of an apparatus containing a pluralityof contactchambers, represented by tubes or pipes R.
Referring first to Fig. 1, M represents a brickwork structure or an iron pipe. lVithin this a pipe R is fixed, leaving the passage S' between. This pipe R consists of two parts co and b, which have different functions and may difer from one another in length and diameter. Also either part can be replaced by aplurality of narrower pipes. The portion b ot' the pipe R is occupied bythe contact substance, (indicated in the drawings by broken section lines,) and this is cooled by the cold air entering the passage S' at n. ln the other part a of the pipe R the gases containing the sulfur dioxid which enter at O are heated to the temperature necessary for the reaction. `When commencing the operation, the whole apparatus is first raised to the temperature necessary for the reaction by heating by means of h 7-say gas-flames. Then, when gases rich in sulfur dioxid are used, after the reaction has once commenced further heating is unnecessary, because the air' as it passes through the pipe M in contact with that part b of the pipe R in which the reaction is in progress in extracting the eXcess of heat due to the reaction absorbs the heat and transfers sufficient heat to the other portion a to prevent a change of position of the reaction zone or the entire cessation of the reaction. The current of air can be regulated by means of the updraft-openings L L, which are adjustable by the' slides Z l. It is regulated in such a Way that the contact substance in b is constantly maintained at the most favorable temperature for the reaction. When the gases contain but little sulfur dioXid, the air, which is somewhat heated by its cooling' action on the contact substance, is further heated by suitable means h' h', (such as gas-flames,) so that the gases in flowing through part a receive a greater increment of heat. When the gases are still poorer in sulfur dioxid, it may be necessary to continually heatto some eX- tent the current of air fiowing in through n, either by means of the gas-flames at h h or in some other way. The gases containing the sulf uric anhydrid issuing from the contact-chamber b leave the apparatus by the pipe O and are worked up in any suitable way.
The apparatus represented in Fi g. 2 is made up of a plurality of contact-tubes R R, which are in connection with one another by means of the two tube-plates W W and the covers D D' above and below. In other respects it resembles Fig. 1.
It will now be Inanifest that in the operation above described there are two independent Currents of gas. One of them-the mixture containing sulfur dioxid and oxygen* passes through the pipe R and is converted. The other current, differently constituted, passes through the' passage adjoining the pipe R, but does not enter the contact material, and performs the function of transferring the eXcess of heat due to the reaction from the part b of the tube R to the part a thereof,
I claim-- 1. The heroin-described process of making sulfuric anhydri'd which consists in passing a gas containing sulfur dioxid and oxygen through a contact substance while removing excess of heat due to the reaction from the contents of the contact-chamber by means of a current ot' fluid which does not enter the contact material, substantially as described;
2. The herein-described process of making sulfuric anhydrid which consists in passing a gas containing sulfur dioxid and oxygen through a contact substa'nce while removing a current of fluid differently constituted from the said gas, substantially as described.
4. The heroin-described process of making i sulfuric anhydrid which consists in passing a current of gas containing sulfur dioXid and oxygen through a contact substance while transferrin g excess of heat due to the reaction` 'from the contact substance to said chamber by means of a second current of fluid differently constituted from and flowin'g in a direction inversely to that of the first-named current, substantially as described.
In testimony whereof I have hereunto set my hand in the presence of two subscribing witnesses.
RUDOLF KNIETSCH.
Witnesses u ERNEST F. EHRHARDT, JACOB ADRIAN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12039A US690062A (en) | 1898-07-14 | 1900-04-07 | Method of making sulfuric anhydrid. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68596998A US652119A (en) | 1898-07-14 | 1898-07-14 | Method of making sulfuric anhydrid. |
| US12039A US690062A (en) | 1898-07-14 | 1900-04-07 | Method of making sulfuric anhydrid. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US690062A true US690062A (en) | 1901-12-31 |
Family
ID=2758604
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US12039A Expired - Lifetime US690062A (en) | 1898-07-14 | 1900-04-07 | Method of making sulfuric anhydrid. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US690062A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2443773A (en) * | 1940-08-24 | 1948-06-22 | Phillips Petroleum Co | Catalytic apparatus |
| US6572835B1 (en) * | 1997-01-24 | 2003-06-03 | The Chemithon Corporation | Method and apparatus for producing gaseous sulfur trioxide |
-
1900
- 1900-04-07 US US12039A patent/US690062A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2443773A (en) * | 1940-08-24 | 1948-06-22 | Phillips Petroleum Co | Catalytic apparatus |
| US6572835B1 (en) * | 1997-01-24 | 2003-06-03 | The Chemithon Corporation | Method and apparatus for producing gaseous sulfur trioxide |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3656900A (en) | Process for the catalytic conversion of sulfur dioxide to sulfur trioxide with production of sulfuric acid | |
| US2236555A (en) | Manufacture of acetylene under modified pressure and temperature conditions | |
| US1917685A (en) | Recovery of sulphur | |
| US3525586A (en) | Production of sulfur trioxide and sulfuric acid | |
| US690062A (en) | Method of making sulfuric anhydrid. | |
| US3915655A (en) | Process and apparatus for burning gas and vapor mixture produced in the purification of coke gas ovens | |
| US2003442A (en) | Manufacture of sulphuric acid from hydrogen sulphide gas | |
| US1894768A (en) | Catalytic apparatus | |
| US3780166A (en) | Process of catalytically reacting so2 to form so3 and of producing sulfuric acid | |
| US2042922A (en) | Process and apparatus for vapor phase catalyses | |
| US2087894A (en) | Recovery of sulphur | |
| US1522166A (en) | Kiln and method of operating same | |
| US2596507A (en) | Manufacture of hcn | |
| US2846291A (en) | Process and apparatus for the production of gases containing sulfur trioxide | |
| US2160610A (en) | Metallurgical furnace | |
| GB1010663A (en) | Improvements in or relating to methods of and apparatus for cooling exhaust gases emerging intermittently from converters or arc furnaces | |
| US2038429A (en) | Contact method of sulphuric acid manufacture | |
| US2087893A (en) | Recovery of sulphur | |
| US688469A (en) | Apparatus for the manufacture of sulfuric anhydrid. | |
| US1995360A (en) | Manufacture of sulphuric acid | |
| US931868A (en) | Process of purifying gases containing sulfur dioxid. | |
| GB991523A (en) | Production of hydrogen-containing gases particularly useful for ammonia synthesis | |
| US1923256A (en) | Process of making contact sulphuric acid | |
| US1547167A (en) | Process for the production of sulphuric acid | |
| US2049243A (en) | Production of sulphuric acid from high oil acid sludges |