US1864496A - Production of nonknocking motor fuels - Google Patents
Production of nonknocking motor fuels Download PDFInfo
- Publication number
- US1864496A US1864496A US381063A US38106329A US1864496A US 1864496 A US1864496 A US 1864496A US 381063 A US381063 A US 381063A US 38106329 A US38106329 A US 38106329A US 1864496 A US1864496 A US 1864496A
- Authority
- US
- United States
- Prior art keywords
- nonknocking
- production
- coal
- motor fuels
- extraction
- 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
- 239000000446 fuel Substances 0.000 title description 7
- 238000004519 manufacturing process Methods 0.000 title description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 20
- 239000000463 material Substances 0.000 description 14
- 230000001066 destructive effect Effects 0.000 description 12
- 238000000605 extraction Methods 0.000 description 12
- 239000003245 coal Substances 0.000 description 10
- 238000005984 hydrogenation reaction Methods 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- 239000010426 asphalt Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000003921 oil Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000003077 lignite Substances 0.000 description 5
- 239000010687 lubricating oil Substances 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 239000012084 conversion product Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000000295 fuel oil Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- VLAPMBHFAWRUQP-UHFFFAOYSA-L molybdic acid Chemical compound O[Mo](O)(=O)=O VLAPMBHFAWRUQP-UHFFFAOYSA-L 0.000 description 2
- 235000002918 Fraxinus excelsior Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- WKQCYNCZDDJXEK-UHFFFAOYSA-N simalikalactone C Natural products C1C(C23C)OC(=O)CC3C(C)C(=O)C(O)C2C2(C)C1C(C)C=C(OC)C2=O WKQCYNCZDDJXEK-UHFFFAOYSA-N 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
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
- C10G1/006—Combinations of processes provided in groups C10G1/02 - C10G1/08
Definitions
- This invention relates to improvements in the production of non-knocking motor fuels from solid non-asphaltic pyrobituminous materials.
- bitumen is intended to include for the purposes of the present invention all those constituents which can be extracted from the
- the increase in the rigor of the successive stages may be eHected by increasing the temperature, the pressure or the duration of the treatment or the quantity of the solvent,vor any of these methods combine l.
- Different solvents may be employed for eac 1 stage if desired.
- fractions of bitumens or their primary conversion products of different kinds are obtained which can each be treated bythemselves and thus yield valuable conversion products, for example solid parain wax, lubricating oils of different consistencies, benzine and the like.
- the separate products obtained may be extracted by means of aromatic solvents under ordinary pressure or they may be subjected to destructive hy rogenation, or to low temperature carbonization or they may be refined by distillaticn.
- the accompanying drawing shows diagrammatically an elevation of a plant which is particularly advantageous for carrying out the process according to the present invention.
- coal is supplied from the coal mill 1 by way of conveyor wheel 2 into the extracting vessel 3 in which it is treated with benzene pumped 1n from container 4 by pump 5.
- Superheated steam is introduced at 6 into the coils 7.
- the stirrer 8 provides for a thorough stirring of the treated materials.
- the materials are then withdrawn from the vessel 3 lat 9 and then passed by way of cooler 10 and y.conveyor Wheel 11 into the filtering device 12 in which the solid coal is separated from the liquid matter. his liquid matter is then subjected to distillation in the still 15 heated by steam introduced at 14.'
- the benzene vapors are carried olf through pipe 13 and condensed in the condenser 16, the condensate being recycled by means of pump 17 into the container 4.
- the residue resulting in the said distillation which consists mainly of bituminous materials extracted from the coal is collected in container 18.
- the coal separated in the filtering device 12 is Withdrawn at 19 and mixed in the mixing vessel 20 with a heavy oil from container 21.
- the mixture is then pumped by pump 22 into the second extracting vessel 23 heated by electrical means 24.
- Stirrer -25 provides for a .thoroughstirring of the treated materials.
- the materials are passed into the cooler 26 and from thence into the container 27.
- the filtering device 28 the coal is separated from the liquid materials, the latter then being conveyed to the still 29 in which the heavy oil ⁇ is separated from the extract.
- the heavy oil vapors areA condensed in the condenser 30 and recycled to the container 21 by pump 31.
- the extract is collected in vessel 32.
- the coal separated in the filtering device 28 is mixed with oil in the vessel 33, the mixture being introduced by means of pump 34 into the preheater 35.
- Initial hydrogen is joined with the said mixture of coal and oil at a point before the preheater 35.
- the preheated materials are then 10. supplied into the high pressure vessel 36 in which they are subjected to destructive hy- Y drogenation.
- the vapors issuing from the vessel 36' are passed into the condenser 37 in which the condensable portions are liquefied.
- the liquids are collected at the bottom of the stripping vessel 38.
- the uncondense'd materials are joined with the initial hydrogen, if desired after having passed'a second con? denser 39 and a purifier 40.
- the liquids collected in the stripping vessel 38 are withdrawn at 41. . Any sludge formed during the destructive hydrogenation is removed from vessel 36 at 42. i A
- Emample 5 Two parts of brown coal rich in bitumen 80 are extracted for about from 1/2 hour to 3/1.
- Bitumen is dissolved out to the extent of from 85 5 to 15 per cent of the initial carbon content and a product is obtained which can be worked up for example into Montan wax or into solid paraiin wax.
- This may be carried out by distilling off the solvent, and if desired treating the product with chromic acid.
- rlwo parts of the residue are then further' extracted with 3 parts of a heavy oil, for examplefanthracene oil, at about 200 atmospheres, at a temperature varying from about 380 to 400 centigrade, 40 to 80 per cent of the original coal content -being thus .removed in all.
- the duration of this extraction is about 1 hour and should preferably not exceed 1 hour and a half.
- the extract can be worked up into lubricating oil by destructive hydrogenation with condensing catalysts. This extraction may be followed and temperature, for example at pressures of upl to about 1000 atmospheres or more, .for exampler 5000 atmospheres and at temperatures of up to about 450 centigrade.
- a product remains, which only contains from 30 to 50, per cent or even less of the original carbon content, and this is de- ,structively hydrogenated under elevated pressure, for example at about 200 atmospheres or more, and even 1000 or 5000 atmospheres with hydrogen at a temperature Y perature and pressure to extract bitumens by a third extraction at still higher pressure.
- a processl for the production of no nknocking motor fuels from brown coal rich in bitumen which comprises subjecting the said brown coal to a treatment by extraction with benzene at pressures ranging between about 1 and 12 atmospheres and at temperatures of between about 200 and 250 C., then subjecting the residue to a further extraction with anthracene oil at about 200 atmospheres and at a vtemperature varying from about 380 to 400 C., then subjecting the residue to a further extraction at pressuresup to about 1000 atmospheres and at temperatures of up to about 450 C., and inally subjecting the residue to destructive hydrogenation at a temperature of about 440 to 450 C. and at a pressure of about 200 atmospheres in the presence of a catalyst prepared from molybdic acid and zinc oxide.
- a process for the. production of nonknocking 'motor Jf'uels from non-asphaltic pyro-bituminous materials having a high bitumen content which comprises subjecting the materials to a treatmentby extraction with aromatic solvents in at least two A successive stages, the first stage being carried out under a high pressure and at a high temperature to extract bitumens suitable for producing paraiiin Wax, subjectin the .extracted residue to extraction at a higher.
- a process for the production of nonknocking motor fuels from brown coal having a high bitumen content which comprises subjecting said coal to an extraction treatment with benzene at an elevated temsuitable for'producing paraiiin wax, subject- A ing the extracted residue to extraction at a higher temperature and pressure with anthracene oil to produceV a product suitable no finally subjecting the residue to destructive hydrogenation to produce low boiling hydrocarbons.
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)
- Working-Up Tar And Pitch (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
M. PIER ET AL PRODUCTIN 0F NONKNOCKING MOTOR FUELS June 2l, :1932.
Filed July 25. 1929 .TIEL- 00 INVENTOR mollzias Pier BY ATTORNEYS Patented June 21, 1932 n UNITED STATESl PAT-ENT ori-ics HATHIAS PIER, 0F HEIDELBERG, AND KURT 'WISSEL OF LUDWIGSHAFEN-ON-THE- l RHINE, GERMANY, ASSIGNORS TO I. G. FARBENINDUSTRIE AKTIENGESELLSCHAFT, 0F FRANKFORT-ON-THE-MAIN, GERMANY, A CORPORATION OF GERMANY l PRODUCTION OF NONKNOCKING MOTOR FUELS Application mea July 25, 1929,'seria1 No. 381,063, and 'in Germany August 22, 192s.
This invention relates to improvements in the production of non-knocking motor fuels from solid non-asphaltic pyrobituminous materials.
A process has already been proposed for 'obtaining non-knocking motor fuels by the destructive. hydrogenation of solid non-as-v phaltic pyrobituminous, materials, such as bituminous coals and even such rich. in bitumens by'taking care that the bitumem which term also comprises its primary vconversion products are not appreciably oo nverted into products of low boiling point range, which can be effected by extracting the bitumen before the destructive hydrogenation, for example, with solvents, which are usuallyA organic and which may be of aromatic nature, or by removing it at an intermediate stage of the said destructive hydrogenation inthe form of solid paraflin Wax or the like, the destructive hydrogenation being carried out under such mild conditions so long as bitumens or their conversion 'products are present in the materials under treatment, that no substantial conversion `of bitumens or their prim ary conversion products takes place thereby. .The term bitumen is intended to include for the purposes of the present invention all those constituents which can be extracted from the pyro-bituminous material by means of a solvent of the nature of benzene and its equivalents'.
We have now found that it is particularly suitable to carry out the said process by removing the bitumens or their primary conversion products in stages, each stage being, preferably, carried out under conditions more rigorous than that preceding it and sub]ect ing the residue to destructive hydrogenation.
If the saidlremoval be effected by extraction with solvents, the increase in the rigor of the successive stages may be eHected by increasing the temperature, the pressure or the duration of the treatment or the quantity of the solvent,vor any of these methods combine l. Different solvents may be employed for eac 1 stage if desired. In this manner fractions of bitumens or their primary conversion products of different kinds are obtained which can each be treated bythemselves and thus yield valuable conversion products, for example solid parain wax, lubricating oils of different consistencies, benzine and the like. Thus for example, the separate products obtained, may be extracted by means of aromatic solvents under ordinary pressure or they may be subjected to destructive hy rogenation, or to low temperature carbonization or they may be refined by distillaticn.
The accompanying drawing shows diagrammatically an elevation of a plant which is particularly advantageous for carrying out the process according to the present invention.
Referring to the drawing in detail coal is supplied from the coal mill 1 by way of conveyor wheel 2 into the extracting vessel 3 in which it is treated with benzene pumped 1n from container 4 by pump 5. Superheated steam is introduced at 6 into the coils 7. The stirrer 8 provides for a thorough stirring of the treated materials. The materials are then withdrawn from the vessel 3 lat 9 and then passed by way of cooler 10 and y.conveyor Wheel 11 into the filtering device 12 in which the solid coal is separated from the liquid matter. his liquid matter is then subjected to distillation in the still 15 heated by steam introduced at 14.' The benzene vapors are carried olf through pipe 13 and condensed in the condenser 16, the condensate being recycled by means of pump 17 into the container 4. The residue resulting in the said distillation Which consists mainly of bituminous materials extracted from the coal is collected in container 18. The coal separated in the filtering device 12 is Withdrawn at 19 and mixed in the mixing vessel 20 with a heavy oil from container 21. The mixture is then pumped by pump 22 into the second extracting vessel 23 heated by electrical means 24. Stirrer -25 provides for a .thoroughstirring of the treated materials. When the extraction is completed the materials are passed into the cooler 26 and from thence into the container 27. In the filtering device 28 the coal is separated from the liquid materials, the latter then being conveyed to the still 29 in which the heavy oil` is separated from the extract. The heavy oil vapors areA condensed in the condenser 30 and recycled to the container 21 by pump 31. The extract is collected in vessel 32. The coal separated in the filtering device 28 is mixed with oil in the vessel 33, the mixture being introduced by means of pump 34 into the preheater 35.
Initial hydrogen is joined with the said mixture of coal and oil at a point before the preheater 35. The preheated materials are then 10. supplied into the high pressure vessel 36 in which they are subjected to destructive hy- Y drogenation. The vapors issuing from the vessel 36' are passed into the condenser 37 in which the condensable portions are liquefied. The liquids are collected at the bottom of the stripping vessel 38. The uncondense'd materials are joined with the initial hydrogen, if desired after having passed'a second con? denser 39 and a purifier 40. The liquids collected in the stripping vessel 38 are withdrawn at 41. .Any sludge formed during the destructive hydrogenation is removed from vessel 36 at 42. i A
The following example will further illustrate the nature of this invention, but the invention is not restricted to this example.
Emample 5 Two parts of brown coal rich in bitumen 80 are extracted for about from 1/2 hour to 3/1.
hour with 4 parts of'benzene at ordinary or slightly elevated pressure; say 12 'atmospheres, and at about 200 to 250 C. Bitumen is dissolved out to the extent of from 85 5 to 15 per cent of the initial carbon content and a product is obtained which can be worked up for example into Montan wax or into solid paraiin wax.
This may be carried out by distilling off the solvent, and if desired treating the product with chromic acid.
rlwo parts of the residue are then further' extracted with 3 parts of a heavy oil, for examplefanthracene oil, at about 200 atmospheres, at a temperature varying from about 380 to 400 centigrade, 40 to 80 per cent of the original coal content -being thus .removed in all. The duration of this extraction is about 1 hour and should preferably not exceed 1 hour and a half. The extract can be worked up into lubricating oil by destructive hydrogenation with condensing catalysts. This extraction may be followed and temperature, for example at pressures of upl to about 1000 atmospheres or more, .for exampler 5000 atmospheres and at temperatures of up to about 450 centigrade.
'Finally a product remains, which only contains from 30 to 50, per cent or even less of the original carbon content, and this is de- ,structively hydrogenated under elevated pressure, for example at about 200 atmospheres or more, and even 1000 or 5000 atmospheres with hydrogen at a temperature Y perature and pressure to extract bitumens by a third extraction at still higher pressure.
- for condensation into lubricating oils and Your hands.
of from 440 to 450 centigrade in the presence of a catalyst prepared from molybdic acid andzinc oxide. Benzine and insome cases also even middle oils and lubricating oils canbe recovered from the liquid product by distillation after removal of the ashes.-
What we claim is:
1. A processl for the production of no nknocking motor fuels from brown coal rich in bitumen, which comprises subjecting the said brown coal to a treatment by extraction with benzene at pressures ranging between about 1 and 12 atmospheres and at temperatures of between about 200 and 250 C., then subjecting the residue to a further extraction with anthracene oil at about 200 atmospheres and at a vtemperature varying from about 380 to 400 C., then subjecting the residue to a further extraction at pressuresup to about 1000 atmospheres and at temperatures of up to about 450 C., and inally subjecting the residue to destructive hydrogenation at a temperature of about 440 to 450 C. and at a pressure of about 200 atmospheres in the presence of a catalyst prepared from molybdic acid and zinc oxide.
2.. A process for the. production of nonknocking 'motor Jf'uels from non-asphaltic pyro-bituminous materials having a high bitumen content which comprises subjecting the materials to a treatmentby extraction with aromatic solvents in at least two A successive stages, the first stage being carried out under a high pressure and at a high temperature to extract bitumens suitable for producing paraiiin Wax, subjectin the .extracted residue to extraction at a higher.
temperature and pressureto produce a product suitable for condensation into lubricating oils and finally subjecting the residue to destructive hydrogenation to produce low boiling hydrocarbons.
3. A process as defined in claim 2 wherein the pyrobituminous material is brown coal.
4. A process for the production of nonknocking motor fuels from brown coal having a high bitumen content which comprises subjecting said coal to an extraction treatment with benzene at an elevated temsuitable for'producing paraiiin wax, subject- A ing the extracted residue to extraction at a higher temperature and pressure with anthracene oil to produceV a product suitable no finally subjecting the residue to destructive hydrogenation to produce low boiling hydrocarbons. f
` In testimony whereof we have hereunto set MATHIAS PIER. KURT-Y WISSEL.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1864496X | 1928-08-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1864496A true US1864496A (en) | 1932-06-21 |
Family
ID=7746617
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US381063A Expired - Lifetime US1864496A (en) | 1928-08-22 | 1929-07-25 | Production of nonknocking motor fuels |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1864496A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2431677A (en) * | 1945-06-08 | 1947-12-02 | Harry D Brown | Process for the recovery of oil from shales |
| US2658861A (en) * | 1948-11-19 | 1953-11-10 | Texas Co | Process for the hydrogenation of coal |
| US3726785A (en) * | 1971-03-03 | 1973-04-10 | Exxon Research Engineering Co | Coal liquefaction using high and low boiling solvents |
| US4036730A (en) * | 1974-05-24 | 1977-07-19 | South African Coal, Oil & Gas Corporation Limited | Solvent-refining of coal |
-
1929
- 1929-07-25 US US381063A patent/US1864496A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2431677A (en) * | 1945-06-08 | 1947-12-02 | Harry D Brown | Process for the recovery of oil from shales |
| US2658861A (en) * | 1948-11-19 | 1953-11-10 | Texas Co | Process for the hydrogenation of coal |
| US3726785A (en) * | 1971-03-03 | 1973-04-10 | Exxon Research Engineering Co | Coal liquefaction using high and low boiling solvents |
| US4036730A (en) * | 1974-05-24 | 1977-07-19 | South African Coal, Oil & Gas Corporation Limited | Solvent-refining of coal |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69920489T2 (en) | INTEGRATED SOLVENT TASTE PACKAGING AND GASIFICATION PROCESS | |
| US4036731A (en) | Hydrogenation of coal | |
| US4028219A (en) | Process for the production of deashed coal liquifaction products | |
| DE2654635A1 (en) | PROCESS FOR THE PRODUCTION OF HYDROCARBON OILS BY CRACKING CARBON HYDRATION | |
| US1881927A (en) | Alfred pott and hans bboche | |
| US2772209A (en) | Recovery of oil from bituminous sands | |
| US1864496A (en) | Production of nonknocking motor fuels | |
| US1838547A (en) | Process for obtaining valuable products from solid carbonaceous materials | |
| DE2919126A1 (en) | PROCESS FOR LIQUID COALING | |
| US2431677A (en) | Process for the recovery of oil from shales | |
| US4464245A (en) | Method of increasing the oil yield from hydrogenation of coal | |
| US1822349A (en) | Recovery of soluble products from solid carbonizable substances | |
| US2223184A (en) | Splitting up of extracts obtained from solid carbonaceous materials | |
| US2215190A (en) | Process for the production of valuable hydrocarbon products by the extraction of solid carbonaceous materials | |
| EP0123161B1 (en) | Process for the hydrogenation of coal | |
| US2572583A (en) | Improved liquid-liquid contacting process using di(beta-cyanoethyl)-amine | |
| US1864855A (en) | Process of producing motor fuel by destructive hydrogenation of carbonaceous materials | |
| US4405437A (en) | Process for coal liquefaction employing a superior coal liquefaction process solvent | |
| DE2803916A1 (en) | Pressure liquefaction of coal - with extn. of prod. by supercritical gas | |
| US3247096A (en) | Hydrocarbon conversion process to produce lubricating oils and waxes | |
| US1904521A (en) | Separation of oils from solid residues | |
| US1920887A (en) | Production of valuable liquid products from solid distillable carbonaceous materialsby destructive hydrogenation | |
| US1921477A (en) | Production of valuable hydrocarbons | |
| US2748061A (en) | Thermal treatment and separation process | |
| US1988019A (en) | Production of hydrocarbons of high boiling point range |