ES294716A1 - Procedimiento para efectuar reacciones de condensaciën de material hidrocarbonado - Google Patents

Procedimiento para efectuar reacciones de condensaciën de material hidrocarbonado

Info

Publication number: ES294716A1
Authority: ES; Spain
Prior art keywords: catalyst; alkylation; benzene; silica; alumina
Prior art date: 1962-12-21
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

Application number

ES0294716A

Other languages

English (en)

Spanish (es)

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Universal Oil Products Co

Original Assignee

Universal Oil Products Co

Priority date (The priority date 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 date listed.)

1962-12-21

Filing date

1963-12-20

Publication date

1964-07-01

1962-12-21 Priority claimed from US246459A external-priority patent/US3205277A/en

1963-12-20 Application filed by Universal Oil Products Co filed Critical Universal Oil Products Co

1964-07-01 Publication of ES294716A1 publication Critical patent/ES294716A1/es

Status Expired legal-status Critical Current

Links

239000003054 catalyst Substances 0.000 title abstract 7
230000005494 condensation Effects 0.000 title abstract 2
238000009833 condensation Methods 0.000 title abstract 2
238000000034 method Methods 0.000 title abstract 2
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 12
238000005804 alkylation reaction Methods 0.000 abstract 5
125000003118 aryl group Chemical group 0.000 abstract 5
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 abstract 4
MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract 4
230000029936 alkylation Effects 0.000 abstract 4
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 4
229910052731 fluorine Inorganic materials 0.000 abstract 4
239000011737 fluorine Substances 0.000 abstract 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 3
239000002131 composite material Substances 0.000 abstract 3
239000007789 gas Substances 0.000 abstract 3
238000006116 polymerization reaction Methods 0.000 abstract 3
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 3
238000010555 transalkylation reaction Methods 0.000 abstract 3
JRZJOMJEPLMPRA-UHFFFAOYSA-N 1-nonene Chemical compound CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
239000005977 Ethylene Substances 0.000 abstract 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
150000001336 alkenes Chemical class 0.000 abstract 2
-1 alkyl sulphates Chemical class 0.000 abstract 2
MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 abstract 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
229910052809 inorganic oxide Inorganic materials 0.000 abstract 2
239000000203 mixture Substances 0.000 abstract 2
YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 abstract 2
OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 abstract 1
239000004215 Carbon black (E152) Substances 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
229910019142 PO4 Inorganic materials 0.000 abstract 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 1
150000001298 alcohols Chemical class 0.000 abstract 1
150000004996 alkyl benzenes Chemical class 0.000 abstract 1
150000001350 alkyl halides Chemical class 0.000 abstract 1
230000002152 alkylating effect Effects 0.000 abstract 1
229910052786 argon Inorganic materials 0.000 abstract 1
150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
235000010290 biphenyl Nutrition 0.000 abstract 1
239000004305 biphenyl Substances 0.000 abstract 1
125000006267 biphenyl group Chemical group 0.000 abstract 1
238000006243 chemical reaction Methods 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
150000001925 cycloalkenes Chemical class 0.000 abstract 1
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
150000002170 ethers Chemical class 0.000 abstract 1
125000002534 ethynyl group Chemical class [H]C#C* 0.000 abstract 1
239000001307 helium Substances 0.000 abstract 1
229910052734 helium Inorganic materials 0.000 abstract 1
SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 abstract 1
229930195733 hydrocarbon Natural products 0.000 abstract 1
150000002430 hydrocarbons Chemical class 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000011261 inert gas Substances 0.000 abstract 1
229910052743 krypton Inorganic materials 0.000 abstract 1
DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 abstract 1
239000000395 magnesium oxide Substances 0.000 abstract 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 1
229910052754 neon Inorganic materials 0.000 abstract 1
GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 abstract 1
229910052757 nitrogen Inorganic materials 0.000 abstract 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
235000021317 phosphate Nutrition 0.000 abstract 1
229920000098 polyolefin Polymers 0.000 abstract 1
JTXAHXNXKFGXIT-UHFFFAOYSA-N propane;prop-1-ene Chemical group CCC.CC=C JTXAHXNXKFGXIT-UHFFFAOYSA-N 0.000 abstract 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
RQFVHGAXCJVPBZ-UHFFFAOYSA-N propylene pentamer Chemical compound CC=C.CC=C.CC=C.CC=C.CC=C RQFVHGAXCJVPBZ-UHFFFAOYSA-N 0.000 abstract 1
239000000376 reactant Substances 0.000 abstract 1
YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 abstract 1
238000000926 separation method Methods 0.000 abstract 1
239000000377 silicon dioxide Substances 0.000 abstract 1
IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 abstract 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 abstract 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 abstract 1
229910052724 xenon Inorganic materials 0.000 abstract 1
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
- 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
- B01J21/04—Alumina
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
- C07C2/66—Catalytic processes
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/02—Boron or aluminium; Oxides or hydroxides thereof
- C07C2521/04—Alumina
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/12—Silica and alumina
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials

Landscapes

Chemical & Material Sciences (AREA)
Organic 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)
Catalysts (AREA)

ES0294716A 1962-12-21 1963-12-20 Procedimiento para efectuar reacciones de condensaciën de material hidrocarbonado Expired ES294716A1 (es)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US24632062A	1962-12-21	1962-12-21
US24631962A	1962-12-21	1962-12-21
US246459A US3205277A (en)	1962-12-21	1962-12-21	Alkylation-transalkylation process

Publications (1)

Publication Number	Publication Date
ES294716A1 true ES294716A1 (es)	1964-07-01

Family

ID=27399916

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0294716A Expired ES294716A1 (es)	1962-12-21	1963-12-20	Procedimiento para efectuar reacciones de condensaciën de material hidrocarbonado

Country Status (7)

Country	Link
BR (1)	BR6355568D0 (de)
CH (1)	CH455719A (de)
DE (1)	DE1442931A1 (de)
DK (1)	DK117554B (de)
ES (1)	ES294716A1 (de)
GB (1)	GB1063489A (de)
SE (1)	SE334600B (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2133032B (en) *	1983-01-07	1986-09-24	Coalite Group Plc	Preparation of dimethylnaphthalenes

1963
- 1963-12-19 DE DE19631442931 patent/DE1442931A1/de active Pending
- 1963-12-20 DK DK598763AA patent/DK117554B/da unknown
- 1963-12-20 ES ES0294716A patent/ES294716A1/es not_active Expired
- 1963-12-20 BR BR155568/63A patent/BR6355568D0/pt unknown
- 1963-12-23 GB GB50623/63A patent/GB1063489A/en not_active Expired
- 1963-12-23 CH CH1587763A patent/CH455719A/de unknown
1967
- 1967-09-01 SE SE12175/67A patent/SE334600B/xx unknown

Also Published As

Publication number	Publication date
GB1063489A (en)	1967-03-30
BR6355568D0 (pt)	1973-07-19
DK117554B (da)	1970-05-11
DE1442931A1 (de)	1969-05-29
CH455719A (de)	1968-05-15
SE334600B (de)	1971-05-03

Publication	Publication Date	Title
US2939890A (en)	1960-06-07	Alkylation of aromatic hydrocarbons
US3551510A (en)	1970-12-29	Alkylation-transalkylation process
EP0358792B1 (de)	1993-03-10	Alkylierungs-/Transalkylierungsverfahren zur selektiven Herstellung von monoalkylierten aromatischen Kohlenwasserstoffen
US5003119A (en)	1991-03-26	Manufacture of alkylbenzenes
US3678120A (en)	1972-07-18	Hydrocarbon conversion catalyst and process
US4857666A (en)	1989-08-15	Alkylation/transalkylation process
US3131230A (en)	1964-04-28	Alkylation of aromatic compounds
KR920001786B1 (ko)	1992-03-02	알킬벤젠의 제조방법
US2372320A (en)	1945-03-27	Hydrocarbon alkylation process
US3531546A (en)	1970-09-29	Alkylation of organic compounds
ES2234512T3 (es)	2005-07-01	Procedimiento para la regeneracion de catalizadores zeoliticos utilizados en procesos de (trans)alquilacion.
US3205277A (en)	1965-09-07	Alkylation-transalkylation process
US3428701A (en)	1969-02-18	Alkylation-transalkylation process
US2395198A (en)	1946-02-19	Alkylation and olefin recovery process
US3631122A (en)	1971-12-28	Alkylation process
US2396682A (en)	1946-03-19	Production of alkyl aromatics
US3068301A (en)	1962-12-11	Alkylation of aromatic hydrocarbons
ES294716A1 (es)	1964-07-01	Procedimiento para efectuar reacciones de condensaciën de material hidrocarbonado
US3436432A (en)	1969-04-01	Process for alkylation of aromatics using a halogen-containing aluminosilicate-alumina catalyst
US2897248A (en)	1959-07-28	Alkylation
US3054836A (en)	1962-09-18	Alkylation of aromatic hydrocarbons
US2416022A (en)	1947-02-18	Alkylation process
US3054835A (en)	1962-09-18	Alkylation of aromatic hydrocarbons
US2541882A (en)	1951-02-13	Alkylation of polynuclear aromatic hydrocarbons
US2971992A (en)	1961-02-14	Alkylation of aromatic hydrocarbons