DE2162614A1 - - Google Patents
Info
- Publication number
- DE2162614A1 DE2162614A1 DE19712162614 DE2162614A DE2162614A1 DE 2162614 A1 DE2162614 A1 DE 2162614A1 DE 19712162614 DE19712162614 DE 19712162614 DE 2162614 A DE2162614 A DE 2162614A DE 2162614 A1 DE2162614 A1 DE 2162614A1
- Authority
- DE
- Germany
- Prior art keywords
- mixture
- zeolite
- catalyst
- polymethylbenzene
- isomerization
- 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.)
- Granted
Links
- 239000003054 catalyst Substances 0.000 claims description 40
- 239000010457 zeolite Substances 0.000 claims description 21
- 238000006317 isomerization reaction Methods 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 20
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 18
- 229910021536 Zeolite Inorganic materials 0.000 claims description 17
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 16
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 claims description 8
- 239000008096 xylene Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 229910000476 molybdenum oxide Inorganic materials 0.000 claims description 6
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 claims description 6
- 150000003863 ammonium salts Chemical class 0.000 claims description 5
- 238000002425 crystallisation Methods 0.000 claims description 5
- 230000008025 crystallization Effects 0.000 claims description 5
- 229910052750 molybdenum Inorganic materials 0.000 claims description 5
- 239000011733 molybdenum Substances 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 239000007789 gas Substances 0.000 claims description 4
- 239000012808 vapor phase Substances 0.000 claims description 4
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 3
- 238000011068 loading method Methods 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 claims 1
- 229940010552 ammonium molybdate Drugs 0.000 claims 1
- 235000018660 ammonium molybdate Nutrition 0.000 claims 1
- 239000011609 ammonium molybdate Substances 0.000 claims 1
- ORVKAVOXRZPETQ-UHFFFAOYSA-N benzene;1,4-xylene Chemical group C1=CC=CC=C1.CC1=CC=C(C)C=C1 ORVKAVOXRZPETQ-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 12
- 238000004821 distillation Methods 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 230000008929 regeneration Effects 0.000 description 6
- 238000011069 regeneration method Methods 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 229910000510 noble metal Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 239000010953 base metal Substances 0.000 description 3
- 230000006698 induction Effects 0.000 description 3
- 238000007086 side reaction Methods 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- -1 ITHnNO ^ 5 -NHj Chemical class 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000010970 precious metal Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000005201 tetramethylbenzenes Chemical class 0.000 description 2
- 150000005199 trimethylbenzenes Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 150000003738 xylenes Chemical class 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- JEWHCPOELGJVCB-UHFFFAOYSA-N aluminum;calcium;oxido-[oxido(oxo)silyl]oxy-oxosilane;potassium;sodium;tridecahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.O.[Na].[Al].[K].[Ca].[O-][Si](=O)O[Si]([O-])=O JEWHCPOELGJVCB-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002751 molybdenum Chemical class 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910001743 phillipsite Inorganic materials 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
Classifications
-
- 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
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
- B01J29/78—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65 containing arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/2702—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously
- C07C5/2708—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously with crystalline alumino-silicates, e.g. molecular sieves
-
- 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
- B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
- B01J2229/30—After treatment, characterised by the means used
- B01J2229/36—Steaming
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S585/00—Chemistry of hydrocarbon compounds
- Y10S585/8995—Catalyst and recycle considerations
- Y10S585/906—Catalyst preservation or manufacture, e.g. activation before use
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00098524A US3848009A (en) | 1970-12-16 | 1970-12-16 | Isomerization of polymethylbenzenes |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2162614A1 true DE2162614A1 (https=) | 1972-07-06 |
| DE2162614B2 DE2162614B2 (de) | 1980-03-13 |
| DE2162614C3 DE2162614C3 (de) | 1980-11-06 |
Family
ID=22269669
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2162614A Expired DE2162614C3 (de) | 1970-12-16 | 1971-12-16 | Verfahren zum Isomerisieren eines nicht im Gleichgewicht befindlichen Polymethylbenzolgemisches |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3848009A (https=) |
| JP (1) | JPS5620289B1 (https=) |
| DE (1) | DE2162614C3 (https=) |
| FR (1) | FR2118112B1 (https=) |
| GB (1) | GB1328918A (https=) |
| NL (1) | NL170131C (https=) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4347397A (en) * | 1981-04-27 | 1982-08-31 | Mobil Oil Corporation | Treatment of effluent resulting from conversion of methanol to gasoline in order to decrease durene and produce distillate |
| US5030787A (en) * | 1990-01-24 | 1991-07-09 | Mobil Oil Corp. | Catalytic disproportionation/transalkylation utilizing a C9+ aromatics feed |
-
1970
- 1970-12-16 US US00098524A patent/US3848009A/en not_active Expired - Lifetime
-
1971
- 1971-12-13 GB GB5774771A patent/GB1328918A/en not_active Expired
- 1971-12-15 FR FR7145163A patent/FR2118112B1/fr not_active Expired
- 1971-12-16 JP JP10225271A patent/JPS5620289B1/ja active Pending
- 1971-12-16 DE DE2162614A patent/DE2162614C3/de not_active Expired
- 1971-12-16 NL NLAANVRAGE7117277,A patent/NL170131C/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| GB1328918A (en) | 1973-09-05 |
| NL7117277A (https=) | 1972-06-20 |
| FR2118112B1 (https=) | 1976-04-16 |
| JPS5620289B1 (https=) | 1981-05-13 |
| DE2162614C3 (de) | 1980-11-06 |
| NL170131B (nl) | 1982-05-03 |
| DE2162614B2 (de) | 1980-03-13 |
| NL170131C (nl) | 1982-10-01 |
| FR2118112A1 (https=) | 1972-07-28 |
| US3848009A (en) | 1974-11-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE19756292C2 (de) | Katalysator zur Umwandlung paraffinischer Kohlenwasserstoffe in korrespondierende Olefine | |
| DE69938318T2 (de) | Katalysator zur Disproportionierung und Transalkylierung von aromatischen Kohlenwasserstoffen und Verfahren zu seiner Herstellung | |
| DE2819267C2 (https=) | ||
| DE3841800A1 (de) | Verfahren und katalysator zur dehydrierung oder dehydrozyklisierung von kohlenwasserstoffen | |
| DE1667704B2 (de) | Verfahren zur herstellung eines katalysators aus einem zeolith und dessen verwendung zur umwandlung von kohlenwasserstoffen | |
| DE1542309A1 (de) | Verfahren zur Herstellung eines edelmetallhaltigen Katalysators | |
| DE1935073C3 (de) | Verfahren zum Reaktivieren eines Festbett-Platinmetall-Aluminiumoxid-Katalysators | |
| DE2261273A1 (de) | Verfahren zur isomerisierung, disporportionierung und/oder umalkylierung von alkylnaphthalinen | |
| DE2414282C2 (de) | Verfahren zur Herstellung sehr reiner aromatischer Kohlenwasserstoffe | |
| CH633504A5 (de) | Verfahren zur dampfphasen-isomerisierung von xylol. | |
| DE69023863T2 (de) | Verfahren zur Herstellung von aromatischen Kohlenwasserstoffen. | |
| DE2531814A1 (de) | Katalysator zur isomerisation von kohlenwasserstoffen | |
| DE2823567C2 (https=) | ||
| DE69915036T2 (de) | Verfahren zur hydrodealkylierung von ethylbenzol und zur isomerisierung von xylol bei niedriger druck | |
| DE2162614A1 (https=) | ||
| DE69112853T2 (de) | Verfahren zur Hestellung eines Katalysators für die Aromatisierung von leichten Kohlenwasserstoffen. | |
| DE1418009C3 (https=) | ||
| DE69001702T2 (de) | Katalysatorzusammensetzung, Verfahren zum Kracken von Nichtaromaten und Verfahren zum Isomerisieren von C8-aromatischen Kohlenwasserstoffen. | |
| DE2723802A1 (de) | Verfahren zur umwandlung von aromatischen kohlenwasserstoffen mit 8 kohlenstoffatomen | |
| DE2806130A1 (de) | Verfahren zur vorbehandlung eines katalysators, der bei der umwandlung von aromatischen kohlenwasserstoffen in einer wasserstoffatmosphaere benutzt wird | |
| DE2513756A1 (de) | Katalysator fuer die wasserstoffbehandlung von kohlenwasserstoffen und dessen herstellung | |
| DE2104131A1 (de) | Verfahren zum Aktivieren von Katalysatoren | |
| DE1442873C3 (https=) | ||
| CH627208A5 (en) | Process for increasing the octane number of a light gasoline fraction | |
| DE918565C (de) | Isomerisieren von Alkylaromaten |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| C3 | Grant after two publication steps (3rd publication) | ||
| 8339 | Ceased/non-payment of the annual fee |