US1599228A - Process and apparatus for exothermic catalytic reactions - Google Patents
Process and apparatus for exothermic catalytic reactions Download PDFInfo
- Publication number
- US1599228A US1599228A US399354A US39935420A US1599228A US 1599228 A US1599228 A US 1599228A US 399354 A US399354 A US 399354A US 39935420 A US39935420 A US 39935420A US 1599228 A US1599228 A US 1599228A
- Authority
- US
- United States
- Prior art keywords
- catalytic
- casing
- naphthalene
- heat
- oxidation
- 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
- 238000000034 method Methods 0.000 title description 7
- 238000006555 catalytic reaction Methods 0.000 title description 5
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 22
- 230000003197 catalytic effect Effects 0.000 description 12
- 238000007254 oxidation reaction Methods 0.000 description 11
- 230000003647 oxidation Effects 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 8
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical class [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 235000010333 potassium nitrate Nutrition 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 235000010344 sodium nitrate Nutrition 0.000 description 2
- 241001527902 Aratus Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241000286904 Leptothecata Species 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002101 lytic effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/87—Benzo [c] furans; Hydrogenated benzo [c] furans
- C07D307/89—Benzo [c] furans; Hydrogenated benzo [c] furans with two oxygen atoms directly attached in positions 1 and 3
-
- 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
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
- B01J8/06—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds in tube reactors; the solid particles being arranged in tubes
Definitions
- This invention relates to catalytic oxidation apparatus and process, and comprises an apparatus which, although of relatively large capacity, is so constructed as to b e operable under precisely controlled conditions.
- One 0f the o jects of my invention is to provide a large scale apparatus wherein the ease of controlling the reaction which is characteristic of small scale operations may be retained.
- Fig. l is a diagrammatic view of a horizontal section through the ap aratus
- Fig. 2 shows a rear elevation with 'part of the condenser broken away.
- the apparatus comprises a casing 2 having in the front end a header or manifold 3 provided with the curved surface 4, and
- tubes 5 Extending lengthwise through said casing, and equally spaced apart, are tubes 5 adapted to be partly illed with catalytic material.
- the condenser 7 Surrounding the pipes 5 and filling the interior of the casing 2 is a medium 5a of high heat conductivity.
- the condenser 7 is provided with an outlet 8 leadingv to any suitable recovery apparatus.
- a burner 9 is disposed 2, both the burner and the casing being supported by brick-work or other sultable frame-work 10.
- An inlet pipe l for introducing a fluid into the apparatus extends into the conduit 6 and through the center of the casing 2.
- the operation may be described with reference to the catalytlc oxidation of naphthalene to phthalic anhydride.
- the interior of the casing 2 having been filled with a material ofvhgh heat conductivity', such as a mixt-ure of sodium and potassium nitrates, and the tubes 5fbeing partly lled withl an oxidation catalyst such as vanadium oxide, the casing 2 and its contents are heated by the burner 9 until the temperature reaches about 500 C.
- a material ofvhgh heat conductivity' such as a mixt-ure of sodium and potassium nitrates
- the burner 9 c an be shut od, the heat of the reaction being more than suiiicient to maintain the temperature at 500 C.
- various other heat conducting materials either solid or liquid, for example, ⁇ other fused salts, materials of high boiling points, such as molten metals, etc.
- the curved surface 4 of the manifold 3 should be such as to distribute the gases uniformly to the several catalytic tubes 5; the best distribution of gases is obtained when this surface is a parabola -of revolution.
- the condenser 7 maybe shaped in various Ways, depending largely upon the material roduced as a result of the catalytic oxi ation. Although the re-heating of the vapors by passing them t rough the casing 2 is desirable, it is not an essential feature of my invention.
- the process of producing phthalic anhydride by the catalytic oxidation of naphth'alene which comprises passing a mixture of naphthalene vapor andan oxygencontaining gas through a plurality of relatively smal, catalytic reaction zones containing an oxidation catalyst at a temperature of from about 400 to 600 C., and causing rapid dissipation of heat in excessof that required to continue the reaction by maintaining said zones in contact with a medium of high heat conductivity.
- the rocess of producing phthalic anhydride which comprises passing a mixture of naphthalene vapor and an oxygencontaining gas through a plurality of small, hot catalytic reaction zones disposed in -a medium of high heat-conductivity.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Description
' beneath the casing Patented Sept. v7, 1926.-
'HARRY n. GIBBs, or' rENNs GaovE, NEW NEMOURS a COMPANY, or WILMINGTO WARE.
PROCESS AND APPARATUS FOR EXOTHERMIC CATALYTIC REACTIONS.
Application led July 27,
This invention relates to catalytic oxidation apparatus and process, and comprises an apparatus which, although of relatively large capacity, is so constructed as to b e operable under precisely controlled conditions.
It is well-known that many oxidation reactions are exothermic, and it is very dilicult to carry on these reactions on a large scale practicable for commercial operatlons, and remove the large amount of heat generated in the process of the reaction. It is also well-known that many ofl these reactions will proceed in very satisfactory manner on a smaller scale, but on a large scale, the concentration of the large amount of heat in the apparatus results in the destruction of the apparatus or the raid combustionl of the desired products o 4the reaction, resultin in unsatisfactory yields.
One 0f the o jects of my invention is to provide a large scale apparatus wherein the ease of controlling the reaction which is characteristic of small scale operations may be retained.
Other objects of the invention will become apparent from the following description.
One embodiment of my invention is shown in the accompanying drawings in which Fig. l is a diagrammatic view of a horizontal section through the ap aratus, and Fig. 2 shows a rear elevation with 'part of the condenser broken away.
The apparatus comprises a casing 2 having in the front end a header or manifold 3 provided with the curved surface 4, and
at the other end a conduit 6 leading into a condenser 7. Extending lengthwise through said casing, and equally spaced apart, are tubes 5 adapted to be partly illed with catalytic material. Surrounding the pipes 5 and filling the interior of the casing 2 is a medium 5a of high heat conductivity. The condenser 7 is provided with an outlet 8 leadingv to any suitable recovery apparatus. A burner 9 is disposed 2, both the burner and the casing being supported by brick-work or other sultable frame-work 10. An inlet pipe l for introducing a fluid into the apparatus extends into the conduit 6 and through the center of the casing 2. Y
1920. Serial No. 399,354.
The operation may be described with reference to the catalytlc oxidation of naphthalene to phthalic anhydride. The interior of the casing 2 having been filled with a material ofvhgh heat conductivity', such as a mixt-ure of sodium and potassium nitrates, and the tubes 5fbeing partly lled withl an oxidation catalyst such as vanadium oxide, the casing 2 and its contents are heated by the burner 9 until the temperature reaches about 500 C. A. mixture of air and naphthalene vapo-rs is then conducted by the pipe `1 through the casing 2, where it becomes preheated, and into the manifold 3 andthen through the catalytic tubes 5, where the naphthalene is oxidized to phthalic anhydride. The mixture of nitrogen, unused oxygen and phthalic anhydride vapor passes into the condenser 7 where the phthalic anhydride condenses and is separated from the permanent ases, the latter escaping through the ue 8.
vAs soon as the oxidation is well started the burner 9 c an be shut od, the heat of the reaction being more than suiiicient to maintain the temperature at 500 C. Instead of a mixture of sodium and potassium nitrates as the heat conducting medium in the casing 2, there may be used various other heat conducting materials, either solid or liquid, for example, `other fused salts, materials of high boiling points, such as molten metals, etc.
The curved surface 4 of the manifold 3 should be such as to distribute the gases uniformly to the several catalytic tubes 5; the best distribution of gases is obtained when this surface is a parabola -of revolution.
With the apparatus above described the catalytic/oxidation of a large amount of a hydrocarbon vapor. such as naphthalene vapor can be effected in a short time, ordinarily at temperatures above 200 O. without losses due to local overheating of the catalytic material with corresponding de- .J'ERSEY, ASSIGNOR TO E. I. DU PONT DE- N, DELAWARE, A CORPORATION 0F DELA--Y composition of the substances to be oxidized.
This desirable result is due to the fact that the medium 5", of high heat conductivity, permits of a rapid and uniform conduction throughout the apparatus of the heat generated in the excess heat being radiated or dissipated about as fast as it is generated. The cata'- several catalytic tubes, the
lytic material is in this way maintained at a uniform temperature throughout the casin 2. v
llthough I have described and shown in detail one specific embodiment of my invention, it will be understood that the apparatus may be changed in various respects without departing from my invention. Thus, the condenser 7 maybe shaped in various Ways, depending largely upon the material roduced as a result of the catalytic oxi ation. Although the re-heating of the vapors by passing them t rough the casing 2 is desirable, it is not an essential feature of my invention.
-.1. The process of producing phthalic anhydride by the catalytic oxidation of naphth'alene which comprises passing a mixture of naphthalene vapor andan oxygencontaining gas through a plurality of relatively smal, catalytic reaction zones containing an oxidation catalyst at a temperature of from about 400 to 600 C., and causing rapid dissipation of heat in excessof that required to continue the reaction by maintaining said zones in contact with a medium of high heat conductivity. 2. The rocess of producing phthalic anhydride liy the catalytic oxidation of naphthalene which comprises passing a mixture of naphthalene vapor and an oxygencontaining gas through a plurality of small, hot catalytic reaction zones disposed in -a medium of high heat-conductivity.
3. The process of producing phthalic anhydride by the catalytic oxidation of naphthalene which comprises passing a mixvture of naphthalene vaporand an oxygencontaining gas through a plurality of small, hot, catalytlc reaction zones evenly disposed in a medium of such high heat .conductivity as to dissipate excess heatl and to maintain said zones at a uniform reacting temperature. y. j
4. The process of producing phthalic anhydride by the catalytic oxidation of naphthalene which comprises passing a. mixture of naphthalene vapor and air through a plurality of relatively small, catalytic reaction zones at a temperature between about 400' and 600 C., and causing rapid dissipation of heat in excess of that required to continue the reaction by maintaining said zones inlcontact with a medium which is a liquid at said temperature and which has ahigh heat-conductlvity.
In testimony whereof I. aix my signature.
-HARRY D. GIBBS.'
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US399354A US1599228A (en) | 1920-07-27 | 1920-07-27 | Process and apparatus for exothermic catalytic reactions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US399354A US1599228A (en) | 1920-07-27 | 1920-07-27 | Process and apparatus for exothermic catalytic reactions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1599228A true US1599228A (en) | 1926-09-07 |
Family
ID=23579206
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US399354A Expired - Lifetime US1599228A (en) | 1920-07-27 | 1920-07-27 | Process and apparatus for exothermic catalytic reactions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1599228A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2567596A (en) * | 1946-03-25 | 1951-09-11 | Phillips Petroleum Co | Synthesis of hydrocarbons |
| US2925319A (en) * | 1953-01-21 | 1960-02-16 | Herbert P A Groll | Process and apparatus for cooling exothermic reactions |
-
1920
- 1920-07-27 US US399354A patent/US1599228A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2567596A (en) * | 1946-03-25 | 1951-09-11 | Phillips Petroleum Co | Synthesis of hydrocarbons |
| US2925319A (en) * | 1953-01-21 | 1960-02-16 | Herbert P A Groll | Process and apparatus for cooling exothermic reactions |
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