CS224625B2 - Method for producing a catalyst,particularly for standard parafines isomerization - Google Patents
Method for producing a catalyst,particularly for standard parafines isomerization Download PDFInfo
- Publication number
- CS224625B2 CS224625B2 CS816315A CS631581A CS224625B2 CS 224625 B2 CS224625 B2 CS 224625B2 CS 816315 A CS816315 A CS 816315A CS 631581 A CS631581 A CS 631581A CS 224625 B2 CS224625 B2 CS 224625B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- catalyst
- solution
- treated
- metal
- deposited
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 59
- 238000004519 manufacturing process Methods 0.000 title claims 2
- 238000006317 isomerization reaction Methods 0.000 title abstract description 19
- 239000000243 solution Substances 0.000 claims abstract description 26
- 239000007864 aqueous solution Substances 0.000 claims abstract description 17
- 239000000203 mixture Substances 0.000 claims abstract description 16
- 150000003868 ammonium compounds Chemical class 0.000 claims abstract description 14
- 239000011260 aqueous acid Substances 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 14
- 229910000510 noble metal Inorganic materials 0.000 claims abstract description 14
- 229910052751 metal Inorganic materials 0.000 claims abstract description 7
- 239000002184 metal Substances 0.000 claims abstract description 7
- 229910001414 potassium ion Inorganic materials 0.000 claims abstract description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 26
- 230000000737 periodic effect Effects 0.000 claims description 18
- 229910052697 platinum Inorganic materials 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 9
- 229910044991 metal oxide Inorganic materials 0.000 claims description 6
- 150000004706 metal oxides Chemical class 0.000 claims description 6
- 238000009835 boiling Methods 0.000 claims description 3
- 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 claims description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 claims 2
- 235000015107 ale Nutrition 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims 1
- 229960005181 morphine Drugs 0.000 claims 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 12
- 238000002360 preparation method Methods 0.000 abstract description 9
- 229910052680 mordenite Inorganic materials 0.000 abstract description 8
- 229910001415 sodium ion Inorganic materials 0.000 abstract description 8
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract description 6
- 239000011591 potassium Substances 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 4
- 150000002739 metals Chemical class 0.000 abstract description 3
- 238000007493 shaping process Methods 0.000 abstract description 3
- 238000011282 treatment Methods 0.000 description 15
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 4
- 238000010306 acid treatment Methods 0.000 description 4
- 238000000151 deposition Methods 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- 239000003929 acidic solution Substances 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000001354 calcination Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000010970 precious metal Substances 0.000 description 3
- 238000007873 sieving Methods 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229910001413 alkali metal ion Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- -1 hydrogen ions Chemical class 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 150000003058 platinum compounds Chemical class 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PXFBZOLANLWPMH-UHFFFAOYSA-N 16-Epiaffinine Natural products C1C(C2=CC=CC=C2N2)=C2C(=O)CC2C(=CC)CN(C)C1C2CO PXFBZOLANLWPMH-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- OTIJDYHLLCTUJA-UHFFFAOYSA-N aluminum oxygen(2-) platinum(2+) Chemical compound [Pt+2].[O-2].[Al+3] OTIJDYHLLCTUJA-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 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
- B01J29/18—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type
- B01J29/20—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type containing iron group metals, noble metals or copper
- B01J29/22—Noble metals
-
- 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
- C07C5/2767—Changing the number of side-chains
- C07C5/277—Catalytic processes
- C07C5/2791—Catalytic processes with metals
-
- 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
- B01J2229/37—Acid treatment
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/02—Gasoline
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL8004797A NL8004797A (nl) | 1980-08-26 | 1980-08-26 | Katalysatorbereiding. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS224625B2 true CS224625B2 (en) | 1984-01-16 |
Family
ID=19835778
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS816315A CS224625B2 (en) | 1980-08-26 | 1981-08-24 | Method for producing a catalyst,particularly for standard parafines isomerization |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US4359409A (ro) |
| EP (1) | EP0046615B1 (ro) |
| JP (1) | JPS5771642A (ro) |
| AR (1) | AR226125A1 (ro) |
| AT (1) | ATE6911T1 (ro) |
| AU (1) | AU542918B2 (ro) |
| BR (1) | BR8105383A (ro) |
| CA (1) | CA1169041A (ro) |
| CS (1) | CS224625B2 (ro) |
| DD (1) | DD200858A5 (ro) |
| DE (1) | DE3162971D1 (ro) |
| DK (1) | DK156267C (ro) |
| ES (1) | ES8301860A1 (ro) |
| MY (1) | MY8500923A (ro) |
| NL (1) | NL8004797A (ro) |
| NO (1) | NO154595C (ro) |
| NZ (1) | NZ198148A (ro) |
| RO (1) | RO83320A (ro) |
| SG (1) | SG68184G (ro) |
| SU (1) | SU1210653A3 (ro) |
| ZA (1) | ZA815831B (ro) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL8004797A (nl) * | 1980-08-26 | 1982-04-01 | Shell Int Research | Katalysatorbereiding. |
| US4575417A (en) * | 1983-03-31 | 1986-03-11 | Texaco Inc. | Process for catalytic dewaxing with mordenite |
| US4536486A (en) * | 1983-03-31 | 1985-08-20 | Texaco Inc. | Process for dewaxing with mordenite |
| FR2579906B1 (ro) * | 1985-04-05 | 1987-05-15 | Inst Francais Du Petrole | |
| US4735929A (en) * | 1985-09-03 | 1988-04-05 | Uop Inc. | Catalytic composition for the isomerization of paraffinic hydrocarbons |
| US4665272A (en) * | 1985-09-03 | 1987-05-12 | Uop Inc. | Catalytic composition for the isomerization of paraffinic hydrocarbons |
| US4665273A (en) * | 1986-02-14 | 1987-05-12 | Uop Inc. | Isomerization of high sulfur content naphthas |
| FR2593084B1 (fr) * | 1986-01-22 | 1990-09-28 | Inst Francais Du Petrole | Catalyseur contenant une mordenite, sa preparation et son application a l'isomerisation de coupes riches en paraffines normales. |
| FR2602696B1 (fr) * | 1986-08-13 | 1988-11-04 | Inst Francais Du Petrole | Catalyseur a base de mordenite pour l'isomerisation de paraffines normales |
| GB2200302A (en) * | 1986-12-05 | 1988-08-03 | South African Inventions | Oligomerization catalyst |
| FR2637200B1 (fr) * | 1988-10-05 | 1991-01-04 | Inst Francais Du Petrole | Catalyseur a base de mordenite renfermant au moins un metal du groupe viii et son utilisation en isomerisation d'une coupe c8 aromatique |
| FR2643830B1 (fr) * | 1989-03-03 | 1991-06-21 | Inst Francais Du Petrole | Catalyseur a base de mordenite renfermant au moins un metal des groupes iia, ivb, iib ou iva et son utilisation en isomerisation d'une coupe c8 aromatique |
| GB8916103D0 (en) * | 1989-07-13 | 1989-08-31 | Shell Int Research | Preparation and use of metal-containing zeolitic catalysts |
| US5225383A (en) * | 1991-05-03 | 1993-07-06 | Amoco Corporation | Distillate hydrogenation catalyst |
| FR2744458B1 (fr) * | 1996-02-05 | 1998-03-27 | Inst Francais Du Petrole | Procede d'isomerisation de paraffines par distillation reactive |
| US8349754B2 (en) * | 2008-03-26 | 2013-01-08 | Council Of Scientific & Industrial Research | Modified zeolite catalyst useful for the conversion of paraffins, olefins and aromatics in a mixed feedstock into isoparaffins and a process thereof |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3376214A (en) * | 1965-09-28 | 1968-04-02 | Standard Oil Co | Hydroforming process with mordenite, alumina and platinum catalyst |
| US3511773A (en) * | 1968-04-29 | 1970-05-12 | Universal Oil Prod Co | Process for producing lpg and a high octane reformate |
| DE1901285A1 (de) * | 1969-01-11 | 1970-08-13 | Feldmuehle Ag | Verfahren und Vorrichtung zum Herstellen von Flaechengebilden |
| US3574092A (en) * | 1969-02-10 | 1971-04-06 | Universal Oil Prod Co | Hydrocarbon conversion process and catalyst therefor |
| DE2044853A1 (de) * | 1969-09-15 | 1971-03-25 | Standard Oil Co , Chicago, 111 (VStA) | Naphtha Hydroformierungs Verfahren |
| CA998989A (en) * | 1970-11-17 | 1976-10-26 | Sun Oil Company Of Pennsylvania | Conversion process using leached mordenite catalyst |
| US3749752A (en) * | 1971-02-19 | 1973-07-31 | Universal Oil Prod Co | Olefin hydroisomerization process |
| US4018711A (en) * | 1971-07-29 | 1977-04-19 | Standard Oil Company (Indiana) | Catalytic composition |
| GB1494314A (en) * | 1974-01-03 | 1977-12-07 | Shell Int Research | Zeolite preparation process |
| US3953320A (en) * | 1974-05-16 | 1976-04-27 | Texaco Inc. | Cracking-isomerization process |
| BE853463A (nl) * | 1976-04-12 | 1977-10-12 | Exxon Research Engineering Co | Katalysator voor het omzetten van koolwaterstoffen |
| NL8004797A (nl) * | 1980-08-26 | 1982-04-01 | Shell Int Research | Katalysatorbereiding. |
-
1980
- 1980-08-26 NL NL8004797A patent/NL8004797A/nl not_active Application Discontinuation
-
1981
- 1981-06-25 US US06/277,359 patent/US4359409A/en not_active Expired - Lifetime
- 1981-07-09 CA CA000381408A patent/CA1169041A/en not_active Expired
- 1981-08-05 EP EP81200885A patent/EP0046615B1/en not_active Expired
- 1981-08-05 AT AT81200885T patent/ATE6911T1/de not_active IP Right Cessation
- 1981-08-21 AR AR286530A patent/AR226125A1/es active
- 1981-08-22 RO RO81105160A patent/RO83320A/ro unknown
- 1981-08-24 BR BR8105383A patent/BR8105383A/pt unknown
- 1981-08-24 ZA ZA815831A patent/ZA815831B/xx unknown
- 1981-08-24 AU AU74469/81A patent/AU542918B2/en not_active Ceased
- 1981-08-24 DD DD81232752A patent/DD200858A5/de not_active IP Right Cessation
- 1981-08-24 NO NO812859A patent/NO154595C/no unknown
- 1981-08-24 CS CS816315A patent/CS224625B2/cs unknown
- 1981-08-24 JP JP56131653A patent/JPS5771642A/ja active Granted
- 1981-08-24 ES ES504918A patent/ES8301860A1/es not_active Expired
- 1981-08-24 SU SU813370200A patent/SU1210653A3/ru active
- 1981-08-24 NZ NZ198148A patent/NZ198148A/xx unknown
- 1981-08-24 DK DK373581A patent/DK156267C/da not_active IP Right Cessation
- 1981-10-05 DE DE8181200885T patent/DE3162971D1/de not_active Expired
-
1982
- 1982-07-16 US US06/399,039 patent/US4400576A/en not_active Expired - Lifetime
-
1984
- 1984-09-21 SG SG681/84A patent/SG68184G/en unknown
-
1985
- 1985-12-30 MY MY923/85A patent/MY8500923A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU7446981A (en) | 1982-03-04 |
| RO83320B (ro) | 1984-03-30 |
| RO83320A (ro) | 1984-03-30 |
| DK373581A (da) | 1982-02-27 |
| AU542918B2 (en) | 1985-03-21 |
| JPH0226541B2 (ro) | 1990-06-11 |
| ES504918A0 (es) | 1983-01-01 |
| DK156267B (da) | 1989-07-24 |
| US4400576A (en) | 1983-08-23 |
| ES8301860A1 (es) | 1983-01-01 |
| JPS5771642A (en) | 1982-05-04 |
| EP0046615B1 (en) | 1984-04-04 |
| SU1210653A3 (ru) | 1986-02-07 |
| NZ198148A (en) | 1983-11-18 |
| SG68184G (en) | 1985-03-15 |
| MY8500923A (en) | 1985-12-31 |
| CA1169041A (en) | 1984-06-12 |
| AR226125A1 (es) | 1982-05-31 |
| DD200858A5 (de) | 1983-06-22 |
| DK156267C (da) | 1989-12-11 |
| ZA815831B (en) | 1982-08-25 |
| US4359409A (en) | 1982-11-16 |
| NL8004797A (nl) | 1982-04-01 |
| BR8105383A (pt) | 1982-08-31 |
| EP0046615A1 (en) | 1982-03-03 |
| NO154595B (no) | 1986-08-04 |
| NO812859L (no) | 1982-03-01 |
| DE3162971D1 (en) | 1984-05-10 |
| ATE6911T1 (de) | 1984-04-15 |
| NO154595C (no) | 1986-11-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CS224625B2 (en) | Method for producing a catalyst,particularly for standard parafines isomerization | |
| EP0474536B1 (fr) | Procédé d'aromatisation des hydrocarbures contenant 2 à 4 atomes de carbone par molécule | |
| JPS6261569B2 (ro) | ||
| US5849652A (en) | Metal containing catalysts and methods for making same | |
| EP0517891B1 (fr) | Zeolithe de type mfi et son procede de preparation | |
| JPH0535019B2 (ro) | ||
| EP0855369B1 (fr) | Zéolithe au phosphore de type structural CON, sa préparation et son utilisation en craquage catalytique | |
| JPS62267242A (ja) | 芳香族炭化水素の製造方法 | |
| CA1300115C (fr) | Catalyseur a base de mordenite pour l'isomerisation de paraffines normales | |
| JPH02157045A (ja) | 第８族の少なくとも１つの金属を含むモルデナイトベース触媒および芳香族ｃ↓８留分の異性化におけるその使用 | |
| JPH08510447A (ja) | ２−メチル−１，５−ジアミノペンタンの触媒環化による３−メチルピペリジンおよび３−メチルピリジンの製造方法 | |
| EP0755717B1 (fr) | Catalyseurs à base de zéolithe mordénite modifié au cérium, et son utilisation en isomérisation d'une coupe C8 aromatique | |
| US4182692A (en) | Mordenite catalyst | |
| EP0440540A1 (fr) | Procédé d'isomérisation de paraffines normales en présence d'au moins un catalyseur à base d'une zéolithe oméga particulière | |
| US5235122A (en) | Zeolite catalysts suitable for hydrocarbon conversion | |
| FR2622473A1 (fr) | Catalyseur d'isomerisation des paraffines normales comprenant une mordenite et du titane | |
| EP0612563B1 (fr) | Catalyseur composite contenant un halogène, un metal noble et au moins un métal additionnel, et son utilisation en aromatisation d'hydrocarbures C2-C12 | |
| CA1092047A (en) | Process for increasing the octane number of a light gasoline fraction | |
| DE60015313T2 (de) | Verfahren zur oxidierung von benzol und/oder toluol zu phenol und/oder cresol | |
| JPH0316644A (ja) | 炭化水素転化に適したゼオライト触媒 | |
| CN1035316A (zh) | 含β沸石的烃重整催化剂 | |
| DE2628262C2 (de) | Katalysator zur Dehydrierung von Paraffinkohlenwasserstoffen zu Olefinen und Verfahren zu seiner Herstellung | |
| JP2555644B2 (ja) | 白金属金族を担持したモルデナイト及びその製造法 | |
| SU857230A1 (ru) | Способ обессеривани легких углеводородов | |
| Oudejans et al. | The decomposition of ethyl diazoacetate over zeolite NaCuX |