GB983473A - Purification of high melting dimethyl naphthalene - Google Patents
Purification of high melting dimethyl naphthaleneInfo
- Publication number
- GB983473A GB983473A GB3426863A GB3426863A GB983473A GB 983473 A GB983473 A GB 983473A GB 3426863 A GB3426863 A GB 3426863A GB 3426863 A GB3426863 A GB 3426863A GB 983473 A GB983473 A GB 983473A
- Authority
- GB
- United Kingdom
- Prior art keywords
- crystals
- solvent
- dissolving
- separating
- alcohol
- 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
- C07C7/00—Purification; Separation; Use of additives
- C07C7/14—Purification; Separation; Use of additives by crystallisation; Purification or separation of the crystals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A dimethylnaphthalene (DMN) mixture melting in the range 100-110.5 DEG C. is obtained from an aromatic hydrocarbon mixture containing DMN by dissolving in a solvent capable of dissolving at least 1 g. of aromatic hydrocarbon boiling in the range 495-510 DEG F. per 10 ml. of solvent at 25 DEG C., crystallizing at at 0 DEG to - 60 DEG C., separating the crystals, warming to 5-50 DEG C. and separating the melt from the crystals which are recovered as product. Preferably the crystals are recrystallized from the same or a similar solvent at 0 DEG to - 60 DEG C. and the crystals may again be partially melted at room temperature. Crystals may be washed at any stage with solvent. Suitable solvents are aliphatic hydrocarbons, e.g. propane, isobutane, n-pentane, n-hexane, heptanes or mixtures thereof with alcohols, e.g. methyl, ethyl, isopropyl, n-butyl, amyl alcohols containing 0-75% by volume of alcohol. A ketone, e.g. acetone or methyl isobutyl ketone may be used with or instead of the alcohol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3426863A GB983473A (en) | 1963-08-29 | 1963-08-29 | Purification of high melting dimethyl naphthalene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3426863A GB983473A (en) | 1963-08-29 | 1963-08-29 | Purification of high melting dimethyl naphthalene |
Publications (1)
Publication Number | Publication Date |
---|---|
GB983473A true GB983473A (en) | 1965-02-17 |
Family
ID=10363525
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3426863A Expired GB983473A (en) | 1963-08-29 | 1963-08-29 | Purification of high melting dimethyl naphthalene |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB983473A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1852409A1 (en) * | 2006-05-01 | 2007-11-07 | Hyosung Corporation | Method for separating and purifying 2,6-dimethylnaphthalene |
-
1963
- 1963-08-29 GB GB3426863A patent/GB983473A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1852409A1 (en) * | 2006-05-01 | 2007-11-07 | Hyosung Corporation | Method for separating and purifying 2,6-dimethylnaphthalene |
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