GB1044163A - Process for the production of 2,6-dimethyl-naphthalene - Google Patents
Process for the production of 2,6-dimethyl-naphthaleneInfo
- Publication number
- GB1044163A GB1044163A GB32910/63A GB3291063A GB1044163A GB 1044163 A GB1044163 A GB 1044163A GB 32910/63 A GB32910/63 A GB 32910/63A GB 3291063 A GB3291063 A GB 3291063A GB 1044163 A GB1044163 A GB 1044163A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dmn
- naphthalene
- dealkylation
- fraction
- crystals
- 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
Links
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
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/24—Polycyclic condensed hydrocarbons containing two rings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D9/00—Crystallisation
- B01D9/0059—General arrangements of crystallisation plant, e.g. flow sheets
-
- 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
- C07C5/2729—Changing the branching point of an open chain or the point of substitution on a ring
- C07C5/2732—Catalytic processes
- C07C5/2735—Catalytic processes with metal oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Naphthalene and 2,6-dimethylnaphthalene (DMN) are obtained from a hydrodesulphurized gas oil boiling in the range 400-900 DEG F. by (1) separating a fraction boiling in the range 500-510 DEG F.; (2) crystallizing this fraction to recover a mixture of 2,6- and 2,7-DMN; (3) dealkylating at above 1000 DEG F. the filtrate from step (2) together with other fractions from step (1) and recycle material from the dealkylation to obtain naphthalene; (4) recrystallizing the mixture from step (2) to recover 2,6-DMN and a concentrate of 2,7-DMN and (5) isomerizing the latter to produce a further mixture of 2,6- and 2,7-DMN recycled to step (2) or (4). The dealkylation product is separated into naphthalene, a 500-520 DEG F. product passed to step (1) and a 450-500 DEG F. fraction recycled to the dealkylation. The mixed 2,6- and 2,7-DMN are crystallized from C3-C7 paraffin, a C1-C5 alcohol or a ketone or mixtures thereof at 0 to - 60 DEG C., the crystals partially melted by warming to 5-50 DEG C. and the crystals recrystallized from a solvent at -30 DEG to -60 DEG C. and the crystals warmed to room temperature.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US283772A US3249644A (en) | 1963-05-28 | 1963-05-28 | Process for the production of 2, 6-dimethylnaphthalene |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1044163A true GB1044163A (en) | 1966-09-28 |
Family
ID=23087482
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32910/63A Expired GB1044163A (en) | 1963-05-28 | 1963-08-20 | Process for the production of 2,6-dimethyl-naphthalene |
Country Status (2)
Country | Link |
---|---|
US (1) | US3249644A (en) |
GB (1) | GB1044163A (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3336411A (en) * | 1964-10-09 | 1967-08-15 | Marathon Oil Co | Process for producing 2, 6-dimethylnaphthalene |
US3485885A (en) * | 1968-04-22 | 1969-12-23 | Sun Oil Co | Process for the purification of 2,6-dimethylnaphthalene |
US3670040A (en) * | 1970-03-01 | 1972-06-13 | Sun Oil Co | Fractionation of c{11 {11 {11 bicyclic aromatic hydrocarbons di or trianhydride complex formation |
US3670039A (en) * | 1970-05-01 | 1972-06-13 | Sun Oil Co | Fractionation of c{11 {11 {11 bicyclic aromatic hydrocarbons by tetrahalophthalic anhydride complex formation |
ES2053664T3 (en) * | 1987-09-24 | 1994-08-01 | Nippon Mining Co | A PROCEDURE FOR PRODUCING DIMETHYLAPHTHALENS. |
US5186816A (en) * | 1990-03-12 | 1993-02-16 | Nippon Mining Co., Ltd. | Method of producing high aromatic-content solvents |
US6057487A (en) * | 1997-12-30 | 2000-05-02 | Chevron Chemical Company | Method for producing 2,6-DMN from mixed dimethylnaphthalenes by crystallization, adsorption and isomerization |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2700638A (en) * | 1950-11-06 | 1955-01-25 | Sinclair Refining Co | Combination cracking process for producing aromatics from petroleum |
US2795633A (en) * | 1952-09-16 | 1957-06-11 | Socony Mobil Oil Co Inc | Demethylation process |
US2750432A (en) * | 1952-09-16 | 1956-06-12 | Socony Mobil Oil Co Inc | Production of naphthalene |
US2958643A (en) * | 1956-08-29 | 1960-11-01 | Sinclair Refining Co | Two-stage catalytic conversion process for producing naphthalene and an aromatic gasoline from cycle oils |
US2858348A (en) * | 1957-03-12 | 1958-10-28 | Sinclair Refining Co | Process for making naphthalene |
US3109036A (en) * | 1961-10-12 | 1963-10-29 | Sun Oil Co | Isomerization of dimethylnaphthalenes |
-
1963
- 1963-05-28 US US283772A patent/US3249644A/en not_active Expired - Lifetime
- 1963-08-20 GB GB32910/63A patent/GB1044163A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US3249644A (en) | 1966-05-03 |
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