US1809114A - Process and apparatus for catalytic reactions - Google Patents
Process and apparatus for catalytic reactions Download PDFInfo
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- US1809114A US1809114A US751802A US75180224A US1809114A US 1809114 A US1809114 A US 1809114A US 751802 A US751802 A US 751802A US 75180224 A US75180224 A US 75180224A US 1809114 A US1809114 A US 1809114A
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- gases
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- catalytic
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- 238000006555 catalytic reaction Methods 0.000 title description 13
- 238000000034 method Methods 0.000 title description 10
- 239000007789 gas Substances 0.000 description 54
- 230000003197 catalytic effect Effects 0.000 description 27
- 238000006243 chemical reaction Methods 0.000 description 21
- 239000000463 material Substances 0.000 description 18
- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulfur dioxide Inorganic materials O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 13
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 11
- 235000010269 sulphur dioxide Nutrition 0.000 description 10
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Inorganic materials O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 9
- 239000006096 absorbing agent Substances 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 6
- 239000002826 coolant Substances 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000000428 dust Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000010276 construction Methods 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 241000286904 Leptothecata Species 0.000 description 1
- 241000219171 Malpighiales Species 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000002101 lytic effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000000126 substance 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
- C01B17/7655—Multi-stage SO3-conversion with intermediate absorption
Definitions
- My invention relates to catalytic processes ⁇ and apparatus, andparticularly to such as are suitable for the conversion of sulfurous anhydride (SO2), in'to sulfuric anhydride (S03).
- SO2 sulfurous anhydride
- S03 sulfuric anhydride
- the object of my invention is to conduct such catalytic reactions under 'conditions of great economy and uniformity of results, and toreducethe size of the apparatus required, thereby saving in factory space and in the cost of the plant.
- A'furtherl object of my invention is yto preserve the apparatus in a working condition without cleaning for a long time, by making specialprovision for the trapping of solid impurities, and particularly dust and scale carried by the gases under treatment.
- FIG. 1 is a diagrammatic elevation of the entire plant adapted for the-conversion of sulfurous acid (SO2) into sulfuric acid
- Figs. 2 and 3 are vertical sections, on an enlarged scale; showing the upper and the lower portions respectively of a column forming part of the apparatus
- Figs. 4 and 5 are horizontal sections onlines 4 4 and 5-5 respectively of Fig. 2
- Fig. 6 is a detail vertical section of a portion of the heat-transferrer.
- a co1- umn-like structure A which, in the particular embodiment shown, comprises live' superposed sections or compartments, of which the upper-most'and lowermost, B and C, as Well as the" middle compartment, D, constitute catalytic converters connected in series, while the two intermediate com artm'ents, E and F (immediately .above an below the middle compartment D), ⁇ are heat-exchangers or:
- the converters B, C, D differ as to the number of layers of catalytic material (between the perforated plates 11), the upper converter having the smallest number of such layers (for instance, live), the middle converter D a larger number (for instance six) and the lower converter C a still larger number for instance, fifteen).
- the purpose of this ierence willx be explained below.
- the lower converter C 1s provided, at the bottom,
- Each of the transferrers E, F is provided with an inlet 15 at the bottom, for ⁇ the admission of the cooling medium, and with an out'- let 16 at the top.
- the horizontal walls or v partitions 17 located above such outlets and below said inlets receive tubes 18 through which the gases undergoing conversion pass downwardly from one converter to the next, while the cooling medium flows in contact with the outer surfaces of the tubes 18, beingl preferably compelled, as by baboards. 19, to fol-4 low a sinuous path.
- a purifier or dust collector for arresting dust and other solid matter suspended in the gases under treatment, and preventing such matter from reaching the converters C and D and impairing their eliciency.
- Such collector may consist of a pan-like body 21 having apertures 22 (generally less in number than the tubes 18) with tubular projections 23 extending upwardly and covered by caps or coWls 24 which act as deflectors to throw any dust or other foreign matter laterally away from the apertures 22 and into the pan-like body 21, whence the matter thus collected may be removed from time to time.
- the outlet 14 is connected by a pipe 25 to the inlet of a cooler 26 (of any suitable construction) the outlet of which is connected by a pipe 27 with the inlet of an absorber 28 which may be of any approved construction suitable for the absorption of the converted gas (that is to say, in the present case,'SO3).
- a pipe 29 to a filter 30 (for instance a coke filter) and then through a pipe 31 and branches 32, 33 to the inlets 15 ofthe transferrers E, F.
- a final converter Gr This may be of the same character as the converters B, C, D, but is more powerful, having a greater number of layers of catalytic material, preferably about as many as the three converters B, D, C, have together.
- the outlets 16 are connected to the inlet of the final converter G by pi es 34, 35. From the outlet of the converter (I the gases pass through a pipe 36 to a cooler 37 and then through a pipe 38 to an absorber 39, to pass subsequently through a pipe 40 to a filter 41 and thence to the stack through a pipe 42.
- the second converter has been made more powerful than the first, by increasing the number of layers of catalytic material. In this second converter, the conversion is carried to the point where about of the original S02 content has been converted into SOS, the temperature rising to about 950 F.
- the gases pass into the lower transferrer F, where'their temperature is again reduced to the original admission temperature (7 50o).
- the cooled gases are then led through the dust-separator interposed between the second transferrer F and the third converter C, and being thus further freed of any solid matter, are brought, at this temperature of about 750 F., into contact with the catalytic material in the converter C.-
- SO2 containing, for instance, from 2 to 2.5% of SO2
- the gases are thus subjected to catalytic action in a plurality of separate converter stages, each containing a successively vincreasing amount of platinum catalytic material, and are cooled intermediate the several conversion stages to the temperature desired for the following conversion.
- the cooler 26 brings the temperature of the gases down to one suitable for the efficient absorption of S03 tol form HZSO., in the absorber 28.
- the remaining gases which are relatively cool and still contain from about 1 to 1.5% of S02, )ass through the filter 30 to the transferrers F, where these gases act as a cooling medium for the hot gases passing through the tube's 18.
- the gases leaving thc transferrers at 16 are brought to a higher temperature, for instance about 800 F., and at this temperature they pass to the linal converterfG, where the conversion of S0: into S03 is completed, or at least carried as far as practical considerations will permit.
- the process is also economical for the reason that the heat of the incoming gases which have undergone partial conversion is suiicient to raise the temperature of the gases used for cooling purposes (that is, the gases from which a large proportion of S03 has been removed in the absorber 28) to the proper point forvthe inal conversion in converter G. j
- An apparatus of the character set forth comprising a plurality of catalytic converters connected in series, a cooler interposed between two successive converters, an absorber having an inlet connected to the outlet of the last of said converters and an outiet connected to the inlet of said cooler, and a final converter connected to the outlet of said cooler, said converters containing catalytic material in an amount increasing from one converter to the next.
- An apparatus of the character set forth comprising a plurality of catalytic converters connected in series, a cooler interposed between two successive converters, an absorber having an inlet connected to the outlet of the last of said converters and an outlet connected to the inlet of said cooler, and a nal con,
- said converters containing catalytic material in an amount increasing from one converter to the next, and the said inal converter oontaining approximately as much catalytic material as the others together.
- An apparatus of the character set forth 4comprising a plurality of catalytic converters connected in series, a plurality of coolers arranged in alternation with said converters, and an absorber having an inlet connected to the outlet of the last of said converters and an outlet connected to the inlets of dierent coolers.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Heat-Exchange Devices With Radiators And Conduit Assemblies (AREA)
Description
June 9, 1931.' l.. GILLETT PROCESS AND APPARATUS FOR CATALYTIC REACTIONS 4 Sheets-Sheet 1 Filed Nov.` 24, 1924 lqllll um. .EESQ wm. m
`zune 9, 1931. 1 GILLET-r 1,809,114
PROCESS AND APPARATUS FOR CATALYTIG REACTIONS Filed Nov. 24, 1924 4 Sheets-Sheet 2 l BMMTWM A TTURNEYS WITNESS June 9, 1931. l.. GILLETT PROCESS APARATUS FOR CATALYTIC REACTIONS Filed Nov. 24, 1924 4 Sheets-Sheet 3 :WE/vrai? 0W/Px 6/1. arr BWKW l L Anonufrs A WITNESS Vif-WWW June 9, 1931.- L. GILLET-r 1 1,809Q1A14 PRocEss AND APPARATUS FOR CATALYTIG REACTIONS Filed Nov. 24, 1924 4 Sheets-Sheet 4 f5. ff
wirf/Ess mvfuron 'Lon/Rr G/LLErr A TTORNEYS Patented June 9, 1931 UNITED vSTATES PATENT ori-*ICEI l 51,'zmaii4A LOWBY GILLETT, OF SYOSSET, NEW YORK, ASSIGNOR TO y(flEhl'llRfAIi CHEMICAL COM- PANY, OF NEW YORK, N. Y., A CORPORATION OF-NEW YORK PROCESS AND APPARATUS FOB, CATA-LYTICAREACTIONS l Application led November 24, 1924. Serial' No. 751,802.
My invention relates to catalytic processes `and apparatus, andparticularly to such as are suitable for the conversion of sulfurous anhydride (SO2), in'to sulfuric anhydride (S03). The object of my invention is to conduct such catalytic reactions under 'conditions of great economy and uniformity of results, and toreducethe size of the apparatus required, thereby saving in factory space and in the cost of the plant. A'furtherl object of my invention is yto preserve the aparatus in a working condition without cleaning for a long time, by making specialprovision for the trapping of solid impurities, and particularly dust and scale carried by the gases under treatment.
. A typical and satisfactor apparatus embodying my. present invention and suitable for carrying out my improvediprocess, is illustrated by the accompanying drawings, in which Fig. 1 is a diagrammatic elevation of the entire plant adapted for the-conversion of sulfurous acid (SO2) into sulfuric acid; Figs. 2 and 3 are vertical sections, on an enlarged scale; showing the upper and the lower portions respectively of a column forming part of the apparatus; Figs. 4 and 5 are horizontal sections onlines 4 4 and 5-5 respectively of Fig. 2; and Fig. 6 is a detail vertical section of a portion of the heat-transferrer.
At 10, I have indicated the inlet through which thel gases to'be treated (for. instance va mixture containing from 10 to 12% of SO2) are admitted to the upper portion of a co1- umn-like structure A which, in the particular embodiment shown, comprises live' superposed sections or compartments, of which the upper-most'and lowermost, B and C, as Well as the" middle compartment, D, constitute catalytic converters connected in series, while the two intermediate com artm'ents, E and F (immediately .above an below the middle compartment D),` are heat-exchangers or:
transferrers. 'I'he two transferrers are constructed alike, and the three converters are of the `same general construction, but di'ifery somewhat in power, as will be explained be- .lo'w.. This construction provides a plurality of, separate converter stages connected in space and secure the plates. The entire carv rier or basket may be removed togetherwith the plates 11 and the catalytic material, as soon as the top of the converter section is opened. As shown in Figs. 2 and 3, the sections of column A are connected in such a way as to' allow them to be taken'apart readily. The converters B, C, D, differ as to the number of layers of catalytic material (between the perforated plates 11), the upper converter having the smallest number of such layers (for instance, live), the middle converter D a larger number (for instance six) and the lower converter C a still larger number for instance, fifteen). The purpose of this ierence willx be explained below. The lower converter C 1s provided, at the bottom,
with an outlet 14. i
Each of the transferrers E, F, is provided with an inlet 15 at the bottom, for` the admission of the cooling medium, and with an out'- let 16 at the top. The horizontal walls or v partitions 17 located above such outlets and below said inlets receive tubes 18 through which the gases undergoing conversion pass downwardly from one converter to the next, while the cooling medium flows in contact with the outer surfaces of the tubes 18, beingl preferably compelled, as by baiiles. 19, to fol-4 low a sinuous path. In order to prevent the gas streams in the tubes 18 from iiowing chiefly along the inner surfaces of said tubes and leaving a relatively stagnant core, it, is advisable to locate a helical wall 20 within each of these tubes, so that the stream will be whirled and all of ifs particles brought in con- `tact with the metallic cooling surfaces.
Between the lower end of each of the transferrers and the upper end of the converter located immediately below, I prefer to arrange a purifier or dust collector for arresting dust and other solid matter suspended in the gases under treatment, and preventing such matter from reaching the converters C and D and impairing their eliciency. Such collector may consist of a pan-like body 21 having apertures 22 (generally less in number than the tubes 18) with tubular projections 23 extending upwardly and covered by caps or coWls 24 which act as deflectors to throw any dust or other foreign matter laterally away from the apertures 22 and into the pan-like body 21, whence the matter thus collected may be removed from time to time.
The outlet 14 is connected by a pipe 25 to the inlet of a cooler 26 (of any suitable construction) the outlet of which is connected by a pipe 27 with the inlet of an absorber 28 which may be of any approved construction suitable for the absorption of the converted gas (that is to say, in the present case,'SO3). From the absorber, the remaining gas passes through a pipe 29 to a filter 30 (for instance a coke filter) and then through a pipe 31 and branches 32, 33 to the inlets 15 ofthe transferrers E, F.
From the outlets 16 of the transferrers the gases pass to a final converter Gr. This may be of the same character as the converters B, C, D, but is more powerful, having a greater number of layers of catalytic material, preferably about as many as the three converters B, D, C, have together. The outlets 16 are connected to the inlet of the final converter G by pi es 34, 35. From the outlet of the converter (I the gases pass through a pipe 36 to a cooler 37 and then through a pipe 38 to an absorber 39, to pass subsequently through a pipe 40 to a filter 41 and thence to the stack through a pipe 42.
The operation, in the case of gases containing, say from 10 to 12% of SO2, is as follows:
These gases, having a temperature of about 750 F., enter at 10 and pass through the Vupper converter B, where about 50% ot the SO2 present-is converted into S03 by thc wellknown catalytic reaction, the temperature of the gases being thereby raised to about 1100 F. The hot gases then pass downwardly through the helical paths within the tubes 18 of the upper transferrer E, and are there cooled to the original admission temperature (750 As the gases issue from the lower ends of the tubes 18, they are not allowed to pass directly to the second converter D, but are deflected by the cowls 24 so that dust and other solid matter will be deflected into the pan-like collector 21, while the gases thus freed of solid matter will pass through the apertures 22 to the second converter D. In view of the fact that the gases admitted to the second converter contain a considerably smaller proportion of SO2 than the gases originally admitted at 10 (the gases entering the second converter may contain, for instance, from 5 to 6% of SO2) the second converter has been made more powerful than the first, by increasing the number of layers of catalytic material. In this second converter, the conversion is carried to the point where about of the original S02 content has been converted into SOS, the temperature rising to about 950 F. At this temperature, the gases pass into the lower transferrer F, where'their temperature is again reduced to the original admission temperature (7 50o The cooled gases are then led through the dust-separator interposed between the second transferrer F and the third converter C, and being thus further freed of any solid matter, are brought, at this temperature of about 750 F., into contact with the catalytic material in the converter C.- The fact that at this point the gases are comparatively rich in S03 and poor in SO2 (containing, for instance, from 2 to 2.5% of SO2) is taken care of by again increasing the number of layers of catalytic material, and thus, when leaving the converter' C through the outlet 14, the gases will have about of the original S02 content converted into S03, and their temperature may be, for instance, about 850 F. It will be seen that the gases are thus subjected to catalytic action in a plurality of separate converter stages, each containing a successively vincreasing amount of platinum catalytic material, and are cooled intermediate the several conversion stages to the temperature desired for the following conversion.
The cooler 26 brings the temperature of the gases down to one suitable for the efficient absorption of S03 tol form HZSO., in the absorber 28. The remaining gases, which are relatively cool and still contain from about 1 to 1.5% of S02, )ass through the filter 30 to the transferrers F, where these gases act as a cooling medium for the hot gases passing through the tube's 18. By this cooling action, as they absorb heat from the gases streaming through the tubes 18, the gases leaving thc transferrers at 16 are brought to a higher temperature, for instance about 800 F., and at this temperature they pass to the linal converterfG, where the conversion of S0: into S03 is completed, or at least carried as far as practical considerations will permit. I have found it desirable to send a-larger portion of the gases from pipe 31 through the. first transferrer E, and a smaller portion through the second transferrer F; for instance, two-thirds of these gases may pass through the pipe 32, and one third through the pipe 33. The cooling action will thus be properly proportioned in view of the fact that the gases enter the tubes 18 of the first transferrer at a considerably higher temperature than the tubes of the second transferrer (1100 and 950 F., respecllG or valves would e place at appropriate points of the pipes, to enable the iow to be controlled or varied as desired, and a blower or like device may be employed to propel or draw the gases through the apparatus. As these elements may be of a well-known type, I have not deemed it necessary to showthem in the drawings. v 4
The advantages of my invention` residein a great simpliication` of the plant, there being but few pipe joints, thereby reducing the changes of leakage. Furthermore, as a minimumnumber of layers of catalytic material is used, the resistance to the flow of the gases is reduced, as are also pressure losses, and-less power is required to cause the gases to pass through the apparatus. A further saving in initial cost and running expenses is effected by the use of a relatively small amount of catalytic material, and by the fact that this material is not allowed to become heated excessively, the heat being removed when the temperature of the gas reaches the point at or above which little or no conversion into SO8 takes place. The process is also economical for the reason that the heat of the incoming gases which have undergone partial conversion is suiicient to raise the temperature of the gases used for cooling purposes (that is, the gases from which a large proportion of S03 has been removed in the absorber 28) to the proper point forvthe inal conversion in converter G. j
Various changes may be made in the specific forms shown and described without departing from the spirit of my invention, as set forth in the claims.
I claim as my invention:
l. The process of carrying out catalytic gas reactions, which consists in subjecting the gases under treatment to a catalytic reaction in successive stages with an amount of catalytic material increasing from one stage to the next, absorbing the gaseous product resulting from such reaction, and using the gases remaining after such absorption, as a cooling medium forthe gases which have become heated by part of the said catalytic reaction.
2. The process of carrying out catalytic gas reactions, which consists in' subjecting the gases under treatment to a partial catalytic reaction in successive stages with an amount of catalytic material increasing from one stage to the next, absorbing the gaseous product resulting from such partial reaction, using the gases remaining after such absorption, as a cooling medium for the gases which have become heated by that part of "the cata'- lytic reaction which precedes said absorption and thereby heating such remaining gases, and then subjecting the remaining gases thus heated, to a further catalytic reaction with an amount of catalytic -material exceeding Suitable cocks that employed in the last preceding catalytic reaction stage.
3` The processof carrying out catalytic i gas reactions, which consists in subjecting the gases under treatment to a catalytic reaction in successive stages with an amount of catalytic material increasing from one stage to the next, absorbing the gaseous product resultin -from such reaction, cooling the gases on their way from one of said reaction stages Ito the next, to approximately their original admission temperature, by means of the unconverted residue of the -gases which have been partially converted by the catalytic reactiomsnbsequently cooled, and have had the product of the conversion removed therefrom by absorption, thereby heating such unconvertef* residue and then subjecting the residue gases thus heated to a further catalytic reaction with an amount of catalytic material exceeding that employed in the last preceding catalytic reaction stage.
4. An apparatus of the character set forth, comprising a plurality of catalytic converters connected in series, a cooler interposed between two successive converters, an absorber having an inlet connected to the outlet of the last of said converters and an outiet connected to the inlet of said cooler, and a final converter connected to the outlet of said cooler, said converters containing catalytic material in an amount increasing from one converter to the next.
5. An apparatus of the character set forth, comprising a plurality of catalytic converters connected in series, a cooler interposed between two successive converters, an absorber having an inlet connected to the outlet of the last of said converters and an outlet connected to the inlet of said cooler, and a nal con,
verter connected to the outlet of said cooler, said converters containing catalytic material in an amount increasing from one converter to the next, and the said inal converter oontaining approximately as much catalytic material as the others together.
6. An apparatus of the character set forth, 4comprising a plurality of catalytic converters connected in series, a plurality of coolers arranged in alternation with said converters, and an absorber having an inlet connected to the outlet of the last of said converters and an outlet connected to the inlets of dierent coolers.
In testimony whereof I have hereunto set my hand. i
LOWRY GILLETT.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US751802A US1809114A (en) | 1924-11-24 | 1924-11-24 | Process and apparatus for catalytic reactions |
| DEG65682D DE442036C (en) | 1924-11-24 | 1925-11-06 | Process and device for the production of sulfuric anhydride by the contact process |
| FR606725D FR606725A (en) | 1924-11-24 | 1925-11-20 | Process and apparatus involving catalytic reactions for the manufacture of sulfur trioxide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US751802A US1809114A (en) | 1924-11-24 | 1924-11-24 | Process and apparatus for catalytic reactions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1809114A true US1809114A (en) | 1931-06-09 |
Family
ID=25023534
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US751802A Expired - Lifetime US1809114A (en) | 1924-11-24 | 1924-11-24 | Process and apparatus for catalytic reactions |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US1809114A (en) |
| DE (1) | DE442036C (en) |
| FR (1) | FR606725A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3034869A (en) * | 1958-05-29 | 1962-05-15 | Scient Design Co | Catalyst retainer |
| US3142536A (en) * | 1960-09-17 | 1964-07-28 | Bayer Ag | Process for the production of sulphur trioxide |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE753027C (en) * | 1940-07-26 | 1953-02-02 | Koppers Gmbh Heinrich | Extraction of sulfur |
| DE1567672B1 (en) * | 1964-07-08 | 1972-04-27 | Metallgesellschaft Ag | Process for the production of SO3 and / or sulfuric acid through the catalytic conversion of gases containing SO2 |
| US3620673A (en) * | 1968-03-21 | 1971-11-16 | Parsons Co Ralph M | Method of producing sulfuric acid |
-
1924
- 1924-11-24 US US751802A patent/US1809114A/en not_active Expired - Lifetime
-
1925
- 1925-11-06 DE DEG65682D patent/DE442036C/en not_active Expired
- 1925-11-20 FR FR606725D patent/FR606725A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3034869A (en) * | 1958-05-29 | 1962-05-15 | Scient Design Co | Catalyst retainer |
| US3142536A (en) * | 1960-09-17 | 1964-07-28 | Bayer Ag | Process for the production of sulphur trioxide |
Also Published As
| Publication number | Publication date |
|---|---|
| DE442036C (en) | 1927-03-22 |
| FR606725A (en) | 1926-06-18 |
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