US1851580A - Manufacture of white oils - Google Patents
Manufacture of white oils Download PDFInfo
- Publication number
- US1851580A US1851580A US263599A US26359928A US1851580A US 1851580 A US1851580 A US 1851580A US 263599 A US263599 A US 263599A US 26359928 A US26359928 A US 26359928A US 1851580 A US1851580 A US 1851580A
- Authority
- US
- United States
- Prior art keywords
- oil
- manufacture
- acid
- hydrogen
- white oils
- 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
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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
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
-
- 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
- C10G71/00—Treatment by methods not otherwise provided for of hydrocarbon oils or fatty oils for lubricating purposes
Definitions
- This invention relates to improvements in the manufacture of high boiling, viscous petroleum products, characterized by relative freedom from coloration, taste, and odor.
- the invention has particular reference to white oils. These include liquid petrolatum U, S. P. and specially refined technical oils of less purity.
- the improved method comprises two principal operations: (1) saturating, stabilizing, and purifying the stock by treatment with hydrogen at high pressure and temperature, and (2) further refining of the stock by chemical and/or physical means.
- the following example is illustrative of my preferred method :
- the stock to be treated for instance a Peruvian or Pennsylvania crude oil, or a heavy fraction of these or similar crudes, is first subjected at a temperature of 750 to 850 F. or thereabouts to a pressure of 50 'to 200 atmospheres of hydrogen gas.
- the reaction is best conducted in a pressure resistant reactor having nonreactive alloy steel surfaces in contact with the oil, which may be supplied as asingle charge or continuously.
- the oil under treatment is agitated by continuous injection of hydrogen
- Catalysts such as a mixture of finely divided metal oxids, especially a mixture of, about 90% chromium oxid and'10% molybdenum oxid, should be kept in suspension in the oil for accelerating the action of the hydrogen. Under the conditions stated, destructive -hydrogenation occurs and sulfur compounds present in the oil are attacked. The sulfur comes off mainly as hydrogen sulfid.
- the cracked and hydrogenated product distills over in admixture with hydrogen, from which it is separated by any suitable condensation, with or without rectification, and the hydrogen is recirculated for further action on the oil in the reactor.
- the particular object of the treatment as carried out for the purpose of the present invention is to secure a substantial proportion of stable, saturated, low-sulfur or sulfur-free distillate of high boiling point and of the required viscosity-that is, from 50 to 600 seconds Saybolt at 100 F.
- the heavier portions of the distillate produced, as described, are excellently suited for the manufacture of White oils, both for j the technical grades of low viscosity, for example 50 to seconds Saybolt at 100 F., and medicinal oils having high viscosity, for example around 400 seconds Saybolt.
- the hydrogenation may advantageously be carried on at temperatures below the cracking range, for example about 650 Fl at a pressure of 100 atmospheres of hydrogen gas.
- the oil is, in this way, hydrogenated only in preparation for the further chemical treatment. Generally, however, destructive hydrogenation is recommended.
- the present invention resides broadly in the combination of hydrogenation and subsequent treating, whereby there is effected a substantial economy in the overall cost of manufacture, as compared with present methods, and the quality of the finished product is also improved, as compared with the product now obtained.
- the undesired constituents of the oil are in part removed by placed'in better form for reaction with the treating agents in the subsequent operations.
- Low'grade stocks,'hitherto considered unsuitable for white oil manufacture, can be used with the present process.
- I claim 1 Process of making a highly purified petroleum oil product, comprising preliminarily heating a petroleum oil of substantially highv er boiling point than the desired product with ration, taste, and odor.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Patented Mar. 29, 1932 UNITED STATES- FRANK A. HOWARD, OF ELIZABETH, NEW ASSIGNOB TO STANDARD OIL DE- 1,ss1,sso
PATENT OFFICE VELOPME NT COMPANY, A CORPORATION OF DELAWARE 'muracrtmn or wnrrr: 011s Ho Drawing.
This invention relates to improvements in the manufacture of high boiling, viscous petroleum products, characterized by relative freedom from coloration, taste, and odor.
The invention has particular reference to white oils. These include liquid petrolatum U, S. P. and specially refined technical oils of less purity. The improved method comprises two principal operations: (1) saturating, stabilizing, and purifying the stock by treatment with hydrogen at high pressure and temperature, and (2) further refining of the stock by chemical and/or physical means. The following example is illustrative of my preferred method :The stock to be treated, for instance a Peruvian or Pennsylvania crude oil, or a heavy fraction of these or similar crudes, is first subjected at a temperature of 750 to 850 F. or thereabouts to a pressure of 50 'to 200 atmospheres of hydrogen gas. The reaction is best conducted in a pressure resistant reactor having nonreactive alloy steel surfaces in contact with the oil, which may be supplied as asingle charge or continuously.
Preferably the oil under treatment is agitated by continuous injection of hydrogen,
,but mechanical agitation may be adopted.
Catalysts such as a mixture of finely divided metal oxids, especially a mixture of, about 90% chromium oxid and'10% molybdenum oxid, should be kept in suspension in the oil for accelerating the action of the hydrogen. Under the conditions stated, destructive -hydrogenation occurs and sulfur compounds present in the oil are attacked. The sulfur comes off mainly as hydrogen sulfid. The cracked and hydrogenated product distills over in admixture with hydrogen, from which it is separated by any suitable condensation, with or without rectification, and the hydrogen is recirculated for further action on the oil in the reactor.
The particular object of the treatment as carried out for the purpose of the present invention is to secure a substantial proportion of stable, saturated, low-sulfur or sulfur-free distillate of high boiling point and of the required viscosity-that is, from 50 to 600 seconds Saybolt at 100 F.
Application filed much 21, 1928. Serial no. 268,599.
(lon'siderable amounts of lighter hydrocarbons are always formed when working at I the temperatures stated. Theseamounts are controllable within limits by proper adjustment of the treating temperature with reference to the hydrogenation efiect and the rate of distillation. The hydrogenation ef-' fectis fixed-by the partial pressure of the hydrogen and the proportion and activity of ating in accordance with well known principles, a satisfactory yield of high boiling products of the desired characteristics may be obtained.
The heavier portions of the distillate produced, as described, are excellently suited for the manufacture of White oils, both for j the technical grades of low viscosity, for example 50 to seconds Saybolt at 100 F., and medicinal oils having high viscosity, for example around 400 seconds Saybolt.
To produce a finished oil from the stable,
saturated, sulfur-free distillate, the latter is treated to remove substantially all the remaining impurities or undesired constituents, leaving an oil which appears to be composed almost exclusively of paraffin and naphthene hydrocarbons 'This treatment is best carried out by reacting upon the oil with sulfuric acid of not less than 98% strength and preferably with fuming acid, at low temperature, and with active mechanicalagitation. The acid should be introduced in successive stages, the separation of the acid and products dissolved in the same being carried out between stages. The total amount of acid employed will depend upon the character of the oil to be produced, but may be 1 from 10 to 50% by volume with reference to the oil treated.
Following the acid treatment,'the oil is washed with caustic soda solution, blown dry and filtered through fullers earth. For
the production of especially good oil, the treatments above referred to may be repeat- 7 used.-
the destructive hydrogenatlon, and in part In some cases, especially when working with oils containing large amounts of unsaturated compounds, either initially present or produced by cracking, the hydrogenation may advantageously be carried on at temperatures below the cracking range, for example about 650 Fl at a pressure of 100 atmospheres of hydrogen gas. The oil is, in this way, hydrogenated only in preparation for the further chemical treatment. Generally, however, destructive hydrogenation is recommended.
' The present invention resides broadly in the combination of hydrogenation and subsequent treating, whereby there is effected a substantial economy in the overall cost of manufacture, as compared with present methods, and the quality of the finished product is also improved, as compared with the product now obtained. The undesired constituents of the oil are in part removed by placed'in better form for reaction with the treating agents in the subsequent operations. Low'grade stocks,'hitherto considered unsuitable for white oil manufacture, can be used with the present process.
-The invention is not to be limited to the specific details given, which are merely illustrative. The hydrogenation may be carried out in any desired way and the subsequent treating may take, any suitable form. Various changes may be made Within the scope of the appended claims, in which it is my intention to claim all novelty inherent v in the invention as broadly as the prior art permits.
I claim 1. Process of making a highly purified petroleum oil product, comprising preliminarily heating a petroleum oil of substantially highv er boiling point than the desired product with ration, taste, and odor.
, 2. Process of making a highly purified petroleum oil product, comprising heating a petroleum fraction of higher boiling range than the desired product to a temperature above about 750 F. under a pressure of 50 to 200 atmospheres of hydrogen gas, taking off a distillate having-a viscosity between about 50 and 600 seconds Saybolt at 100 F treat- 7 ing the distillate. with sulfuric acid of not less than 98% strength to i'emove substantially all undesired constituents of the oil,
and separating the purified oil from the acid reaction products and residual acid, to produce an oil substantially free from coloration, taste,,and odor.
3. Process of making a highly purified substantially sulfur-free, odorless, colorless and late with sulfuric acid of not less than 98% strength, and separating the purified distillate from the excess acid and acid extraction products.
FRANK A. HOWARD.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US263599A US1851580A (en) | 1928-03-21 | 1928-03-21 | Manufacture of white oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US263599A US1851580A (en) | 1928-03-21 | 1928-03-21 | Manufacture of white oils |
Publications (1)
Publication Number | Publication Date |
---|---|
US1851580A true US1851580A (en) | 1932-03-29 |
Family
ID=23002458
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US263599A Expired - Lifetime US1851580A (en) | 1928-03-21 | 1928-03-21 | Manufacture of white oils |
Country Status (1)
Country | Link |
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US (1) | US1851580A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3328293A (en) * | 1963-04-25 | 1967-06-27 | British Petroleum Co | Preparation of white oils and liquid paraffins |
US3330758A (en) * | 1964-07-27 | 1967-07-11 | Atlantic Richfield Co | Motor fuel blend containing hydrogenated heavy cracked naphtha |
-
1928
- 1928-03-21 US US263599A patent/US1851580A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3328293A (en) * | 1963-04-25 | 1967-06-27 | British Petroleum Co | Preparation of white oils and liquid paraffins |
US3330758A (en) * | 1964-07-27 | 1967-07-11 | Atlantic Richfield Co | Motor fuel blend containing hydrogenated heavy cracked naphtha |
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