JPH0427216B2 - - Google Patents
Info
- Publication number
- JPH0427216B2 JPH0427216B2 JP60297619A JP29761985A JPH0427216B2 JP H0427216 B2 JPH0427216 B2 JP H0427216B2 JP 60297619 A JP60297619 A JP 60297619A JP 29761985 A JP29761985 A JP 29761985A JP H0427216 B2 JPH0427216 B2 JP H0427216B2
- Authority
- JP
- Japan
- Prior art keywords
- methylnaphthalene
- monoethanolamine
- distilled
- hydrocarbon oil
- fraction
- 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 - Lifetime
Links
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 claims description 100
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 19
- 239000004215 Carbon black (E152) Substances 0.000 claims description 16
- 229930195733 hydrocarbon Natural products 0.000 claims description 16
- 150000002430 hydrocarbons Chemical class 0.000 claims description 16
- 238000004821 distillation Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 239000003921 oil Substances 0.000 description 21
- QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical compound C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 14
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
- 238000000926 separation method Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 6
- 239000002994 raw material Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000006477 desulfuration reaction Methods 0.000 description 4
- 230000023556 desulfurization Effects 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 150000002391 heterocyclic compounds Chemical class 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- -1 bicyclic aromatic compounds Chemical class 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000011280 coal tar Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 150000002898 organic sulfur compounds Chemical class 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical class C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 1
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000000895 extractive distillation Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002475 indoles Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29761985A JPS62153232A (ja) | 1985-12-26 | 1985-12-26 | メチルナフタレンを分離する方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29761985A JPS62153232A (ja) | 1985-12-26 | 1985-12-26 | メチルナフタレンを分離する方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62153232A JPS62153232A (ja) | 1987-07-08 |
JPH0427216B2 true JPH0427216B2 (no) | 1992-05-11 |
Family
ID=17848900
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29761985A Granted JPS62153232A (ja) | 1985-12-26 | 1985-12-26 | メチルナフタレンを分離する方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62153232A (no) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108586184B (zh) * | 2018-04-17 | 2021-03-30 | 鹏辰新材料科技股份有限公司 | 一种基于超临界和超声波的β-甲基萘的分离和精制方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6036427A (ja) * | 1983-08-08 | 1985-02-25 | Sumikin Coke Co Ltd | メチルナフタレン含有炭化水素油からメチルナフタレンを分離する方法 |
-
1985
- 1985-12-26 JP JP29761985A patent/JPS62153232A/ja active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6036427A (ja) * | 1983-08-08 | 1985-02-25 | Sumikin Coke Co Ltd | メチルナフタレン含有炭化水素油からメチルナフタレンを分離する方法 |
Also Published As
Publication number | Publication date |
---|---|
JPS62153232A (ja) | 1987-07-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2817393B1 (en) | Regeneration of selective solvents for extractive processes | |
USRE26255E (en) | Recovery of aromatics | |
US3173966A (en) | Solvent extraction process for recovery of aromatic hydrocarbons | |
US3338824A (en) | Water-washing raffinate to recover the sulfolane solvent | |
GB1430481A (en) | Process for purifying benezene and toluene by extractive azeotropic distillation process for producing aromatic hydrocarbons | |
US2831905A (en) | Gamma-butyrolactone as a selective solvent for hydrocarbons | |
US2957811A (en) | Segregation of xylene isomers | |
US2727854A (en) | Recovery of naphthalene | |
US2786085A (en) | Solvent extraction process applied to feed stocks of high boiling points | |
JPH0427216B2 (no) | ||
US2848387A (en) | Separation of aromatic and nonaromatic hydrocarbons | |
US2183852A (en) | Solvent extraction | |
US2952717A (en) | Separation of hydrocarbons by dual solvent extraction | |
US3299158A (en) | Production of pure aromatic hydrocarbons | |
US3449462A (en) | Separation process | |
US3120487A (en) | Solvent extraction with alkyl substituted 2-oxazolidones | |
US2386755A (en) | Purification of hydrocarbons by azeotropic distillation | |
JPS636531B2 (no) | ||
JPS63410B2 (no) | ||
US3560374A (en) | Aromatic extraction process | |
US3247101A (en) | Hydrocarbon treating process | |
JPS62153233A (ja) | 2−メチルナフタレンの精製方法 | |
JPH0378853B2 (no) | ||
SU1161505A1 (ru) | Экстрагент дл выделени ароматических углеводородов @ - @ | |
US2465717A (en) | Isolation of styrene by azeotropic distillation with ethylene chlorohydrin |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
EXPY | Cancellation because of completion of term |