IL26181A - Simultaneous preparation of saturated elliptical hydrocarbons containing 1 to 4 atoms of carbon, and benzene and its homologues, from light crude oil - Google Patents
Simultaneous preparation of saturated elliptical hydrocarbons containing 1 to 4 atoms of carbon, and benzene and its homologues, from light crude oilInfo
- Publication number
- IL26181A IL26181A IL26181A IL2618166A IL26181A IL 26181 A IL26181 A IL 26181A IL 26181 A IL26181 A IL 26181A IL 2618166 A IL2618166 A IL 2618166A IL 26181 A IL26181 A IL 26181A
- Authority
- IL
- Israel
- Prior art keywords
- hydrocarbons
- saturated
- hydrogen
- aromatics
- light naphtha
- Prior art date
Links
- 229920006395 saturated elastomer Polymers 0.000 title claims description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 title description 33
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 title description 3
- 238000002360 preparation method Methods 0.000 title description 3
- 239000001257 hydrogen Substances 0.000 claims description 40
- 229910052739 hydrogen Inorganic materials 0.000 claims description 40
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 35
- 229930195733 hydrocarbon Natural products 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 26
- 150000002430 hydrocarbons Chemical class 0.000 claims description 24
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 17
- 239000003054 catalyst Substances 0.000 claims description 16
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 14
- 239000005977 Ethylene Substances 0.000 claims description 14
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 14
- 239000000047 product Substances 0.000 claims description 14
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 12
- 238000006356 dehydrogenation reaction Methods 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 7
- 238000004227 thermal cracking Methods 0.000 claims description 7
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- 239000011368 organic material Substances 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 239000012263 liquid product Substances 0.000 claims 1
- 230000000063 preceeding effect Effects 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000007789 gas Substances 0.000 description 16
- 125000003118 aryl group Chemical group 0.000 description 13
- 238000009835 boiling Methods 0.000 description 9
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 8
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 238000000926 separation method Methods 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 239000008096 xylene Substances 0.000 description 6
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 229940058172 ethylbenzene Drugs 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- 239000001273 butane Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical class [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000004517 catalytic hydrocracking Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000008246 gaseous mixture Substances 0.000 description 2
- 238000006317 isomerization reaction Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 238000001833 catalytic reforming Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000004230 steam cracking Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- FHYUCVWDMABHHH-UHFFFAOYSA-N toluene;1,2-xylene Chemical group CC1=CC=CC=C1.CC1=CC=CC=C1C FHYUCVWDMABHHH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/58—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to change the structural skeleton of some of the hydrocarbon content without cracking the other hydrocarbons present, e.g. lowering pour point; Selective hydrocracking of normal paraffins
- C10G45/68—Aromatisation of hydrocarbon oil fractions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C9/00—Aliphatic saturated hydrocarbons
- C07C9/14—Aliphatic saturated hydrocarbons with five to fifteen carbon atoms
-
- 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
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL6509667A NL6509667A (enrdf_load_stackoverflow) | 1965-07-26 | 1965-07-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
IL26181A true IL26181A (en) | 1970-06-17 |
Family
ID=19793744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL26181A IL26181A (en) | 1965-07-26 | 1966-07-20 | Simultaneous preparation of saturated elliptical hydrocarbons containing 1 to 4 atoms of carbon, and benzene and its homologues, from light crude oil |
Country Status (12)
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3926779A (en) * | 1974-01-21 | 1975-12-16 | Texaco Inc | Upgrading of paraffinic gasoline blending components by cyclization with a platinum/magnesium oxide alumina matrix catalyst |
NZ211005A (en) * | 1984-02-02 | 1988-03-30 | Terje Rosenlund | Impregnating wood |
DE102004011553A1 (de) * | 2004-03-08 | 2005-10-06 | Betriebsforschungsinstitut VDEh - Institut für angewandte Forschung GmbH | Messvorrichtung und Messverfahren zur Zustandsbestimmung eines Metallschmelzenstroms |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2143472A (en) * | 1936-07-20 | 1939-01-10 | Shell Dev | Process for treating hydrocarbons |
US2908628A (en) * | 1956-06-28 | 1959-10-13 | Sun Oil Co | Hydrocarbon conversion |
DE1470593A1 (de) * | 1961-02-03 | 1969-02-13 | Metallgesellschaft Ag | Verfahren zur Erzeugung von Aromaten und olefinischen Kohlenwasserstoffen |
US3198728A (en) * | 1962-06-20 | 1965-08-03 | Socony Mobil Oil Co Inc | Method of improving front end octane rating and increasing "lpg" production |
-
0
- NL NL128679D patent/NL128679C/xx active
-
1965
- 1965-07-26 NL NL6509667A patent/NL6509667A/xx unknown
-
1966
- 1966-07-19 GB GB32430/66A patent/GB1133263A/en not_active Expired
- 1966-07-20 IL IL26181A patent/IL26181A/en unknown
- 1966-07-22 AT AT703366A patent/AT269321B/de active
- 1966-07-22 CH CH1068366A patent/CH473071A/de not_active IP Right Cessation
- 1966-07-23 ES ES0329427A patent/ES329427A1/es not_active Expired
- 1966-07-25 NO NO164051A patent/NO118557B/no unknown
- 1966-07-25 DE DEST25686A patent/DE1276265B/de active Pending
- 1966-07-26 SE SE10183/66A patent/SE341390B/xx unknown
- 1966-07-26 US US567940A patent/US3455813A/en not_active Expired - Lifetime
- 1966-07-26 DK DK387766A patent/DK132399C/da active
- 1966-07-26 BE BE684601D patent/BE684601A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
ES329427A1 (es) | 1967-09-01 |
SE341390B (enrdf_load_stackoverflow) | 1971-12-27 |
CH473071A (de) | 1969-05-31 |
AT269321B (de) | 1969-03-10 |
DK132399C (da) | 1976-05-03 |
BE684601A (enrdf_load_stackoverflow) | 1967-01-26 |
NL6509667A (enrdf_load_stackoverflow) | 1967-01-27 |
NO118557B (enrdf_load_stackoverflow) | 1970-01-12 |
GB1133263A (en) | 1968-11-13 |
DK132399B (da) | 1975-12-01 |
NL128679C (enrdf_load_stackoverflow) | |
DE1276265B (de) | 1968-08-29 |
US3455813A (en) | 1969-07-15 |
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