GB494834A - Improvements in or relating to the extraction of bituminous or brown coal and like solid carbonaceous materials with solvents at high temperatures - Google Patents
Improvements in or relating to the extraction of bituminous or brown coal and like solid carbonaceous materials with solvents at high temperaturesInfo
- Publication number
- GB494834A GB494834A GB292037A GB292037A GB494834A GB 494834 A GB494834 A GB 494834A GB 292037 A GB292037 A GB 292037A GB 292037 A GB292037 A GB 292037A GB 494834 A GB494834 A GB 494834A
- Authority
- GB
- United Kingdom
- Prior art keywords
- kgs
- hydrogenation
- extract
- naphthalene
- tetrahydronaphthalene
- 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
- 238000000605 extraction Methods 0.000 title abstract 5
- 239000002904 solvent Substances 0.000 title abstract 5
- 239000002802 bituminous coal Substances 0.000 title abstract 2
- 239000003575 carbonaceous material Substances 0.000 title abstract 2
- 239000007787 solid Substances 0.000 title abstract 2
- 239000003077 lignite Substances 0.000 title 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 12
- 238000005984 hydrogenation reaction Methods 0.000 abstract 8
- 239000003795 chemical substances by application Substances 0.000 abstract 5
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 abstract 5
- 150000001896 cresols Chemical class 0.000 abstract 4
- 238000009835 boiling Methods 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- 239000003502 gasoline Substances 0.000 abstract 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 abstract 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- 230000001066 destructive effect Effects 0.000 abstract 2
- 238000004821 distillation Methods 0.000 abstract 2
- 239000007789 gas Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 229910001570 bauxite Inorganic materials 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000003245 coal Substances 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 229930003836 cresol Natural products 0.000 abstract 1
- 239000012467 final product Substances 0.000 abstract 1
- 239000000295 fuel oil Substances 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000012263 liquid product Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 229910001507 metal halide Inorganic materials 0.000 abstract 1
- 150000005309 metal halides Chemical class 0.000 abstract 1
- 230000004048 modification Effects 0.000 abstract 1
- 238000012986 modification Methods 0.000 abstract 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 238000007670 refining Methods 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- ITRNXVSDJBHYNJ-UHFFFAOYSA-N tungsten disulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 abstract 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
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/08—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts
- C10G1/083—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts in the presence of a solvent
-
- 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
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/002—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal in combination with oil conversion- or refining processes
-
- 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
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/04—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
- C10G1/042—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction by the use of hydrogen-donor solvents
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
In the pressure extraction of solid carbonaceous materials with solvents followed by destructive hydrogenation of the extract obtained, the extraction agent employed comprises a fraction boiling between 170 to 260 DEG C. and containing 5-40 per cent cresols by weight which has been obtained from the products produced by destructive hydrogenation of a previous extract. The heavy residues from the hydrogenation process are preferably recycled as pasting agent for further initial material to be extracted, the said residues being collected as liquids without substantial cooling from the hot reaction products issuing from the reaction vessel. The extraction is carried out at 250-470 DEG C. and under pressures of 20-500 atmos. for 30 to 60 mins. in the presence of catalysts, e.g. metal halides, and if desired in presence of limited amounts of hydrogen. Naphthalene may be added to the used hydrogenation extract to increase the content of tetrahydronaphthalene or may be removed therefrom by distillation. In the example, 435 kgs. ground bituminous coal are pasted with 700 kgs. solvent comprising 420 kgs. tetrahydronaphthalene, 140 kgs. naphthalene, and 140 kgs. cresols, and the paste is extracted at 410-430 DEG C. at pressures increasing from 80 to 105 atmos.; 300 kgs. pressure extract and 700 kgs. extraction agent are obtained, the latter comprising 280 kgs. <PICT:0494834/III/1> <PICT:0494834/III/2> <PICT:0494834/III/3> is mixed with 555 kgs. of pasting oil comprising sludgy residues obtained from the hot catchpot of a previous hydrogenation and which contains already as catalyst 5-7 per cent of iron oxide obtained as a residue from the chemical disintegration of bauxite by sodium carbonate. The mixture is destructively hydrogenated at 470-480 DEG C. under a pressure of 650 atmos. and a product is obtained comprising 70 kgs. gases and 11 kgs. water and liquid products which are topped to remove gasoline boiling below 190 DEG C. The fraction boiling between 190 and 225 DEG C. is recovered and 700 kgs. of this fraction comprising 420 kgs. tetrahydronaphthalene, 140 kgs. naphthalene, and 140 kgs. cresols are separated and used as extracting agent for fresh coal. The remainder of this fraction is mixed with the gasoline fraction and subjected to a refining hydrogenation at 475 DEG C. tetrahydronaphthalene, 280 kgs. naphthalene, and 140 kgs. cresols (one-third of the tetrohydronaphthalene is thus converted into naphthalene). The mixture of extract and extracting agent and 50 atmos. pressure in presence of a stationary catalyst comprising tungsten disulphide, and a final product comprising 70 kgs. gases, 11 kgs. water, 112 kgs. gasoline (octane number 92) and 177 kgs. fuel oil (viscosity, 1,5 Engler at 20 DEG C. and pour point, 50 DEG C.) is obtained. The method of operation is shown diagrammatically in Fig. 1, while in Fig. 2 the process is modified by separating by distillation the tetrahydronaphthalene and cresol from the extract prior to the hydrogenation stage. The separation may be carried out before or after the hot residues have been added to the extract. A further modification is shown in Fig. 4, according to which the separated solvent with or without addition or removal of naphthalene is subjected to hydrogenation prior to re-use as solvent. Specification 283,545, [Class 91], is referred to.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB292037A GB494834A (en) | 1937-02-01 | 1937-02-01 | Improvements in or relating to the extraction of bituminous or brown coal and like solid carbonaceous materials with solvents at high temperatures |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB292037A GB494834A (en) | 1937-02-01 | 1937-02-01 | Improvements in or relating to the extraction of bituminous or brown coal and like solid carbonaceous materials with solvents at high temperatures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB494834A true GB494834A (en) | 1938-11-01 |
Family
ID=9748557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB292037A Expired GB494834A (en) | 1937-02-01 | 1937-02-01 | Improvements in or relating to the extraction of bituminous or brown coal and like solid carbonaceous materials with solvents at high temperatures |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB494834A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2412600A1 (en) * | 1977-12-21 | 1979-07-20 | South African Coal Oil Gas | PROCESS FOR THE LIQUEFACTION OF COAL |
| EP0047571A3 (en) * | 1980-09-09 | 1982-06-09 | The Pittsburgh & Midway Coal Mining Company | Short residence time coal liquefaction process including catalytic hydrogenation |
| GB2138839A (en) * | 1983-02-28 | 1984-10-31 | Sasol Operations Pty Ltd | Refining of coal |
| US4521291A (en) * | 1982-02-09 | 1985-06-04 | Coal Industry (Patents) Limited | Coal extraction |
| GB2152071A (en) * | 1983-12-30 | 1985-07-31 | Inst Chemii Przemyslowej | Method for separating volatile matter from solid coal residues |
| GB2175915A (en) * | 1985-06-01 | 1986-12-10 | British Petroleum Co Plc | Process for obtaining lower molecular weight materials from coal |
| CN117185893A (en) * | 2023-09-07 | 2023-12-08 | 黄淮学院 | A heat-integrated multi-column distillation method for separating tetralin and o-, m- and p-cresol mixtures |
-
1937
- 1937-02-01 GB GB292037A patent/GB494834A/en not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2412600A1 (en) * | 1977-12-21 | 1979-07-20 | South African Coal Oil Gas | PROCESS FOR THE LIQUEFACTION OF COAL |
| EP0047571A3 (en) * | 1980-09-09 | 1982-06-09 | The Pittsburgh & Midway Coal Mining Company | Short residence time coal liquefaction process including catalytic hydrogenation |
| US4521291A (en) * | 1982-02-09 | 1985-06-04 | Coal Industry (Patents) Limited | Coal extraction |
| GB2138839A (en) * | 1983-02-28 | 1984-10-31 | Sasol Operations Pty Ltd | Refining of coal |
| GB2152071A (en) * | 1983-12-30 | 1985-07-31 | Inst Chemii Przemyslowej | Method for separating volatile matter from solid coal residues |
| GB2175915A (en) * | 1985-06-01 | 1986-12-10 | British Petroleum Co Plc | Process for obtaining lower molecular weight materials from coal |
| CN117185893A (en) * | 2023-09-07 | 2023-12-08 | 黄淮学院 | A heat-integrated multi-column distillation method for separating tetralin and o-, m- and p-cresol mixtures |
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