US1934068A - Process for treating synthetic oils - Google Patents
Process for treating synthetic oils Download PDFInfo
- Publication number
- US1934068A US1934068A US500424A US50042430A US1934068A US 1934068 A US1934068 A US 1934068A US 500424 A US500424 A US 500424A US 50042430 A US50042430 A US 50042430A US 1934068 A US1934068 A US 1934068A
- Authority
- US
- United States
- Prior art keywords
- oil
- oils
- chlorine
- halides
- condensation
- 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
- 239000003921 oil Substances 0.000 title description 27
- 238000000034 method Methods 0.000 title description 17
- 229910052801 chlorine Inorganic materials 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 14
- 150000004820 halides Chemical class 0.000 description 14
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 13
- 238000009833 condensation Methods 0.000 description 10
- 230000005494 condensation Effects 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 239000010687 lubricating oil Substances 0.000 description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 230000008018 melting Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B61/00—Other general methods
-
- 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
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
Definitions
- the present invention relates to an improved method for treating lubricating oils andmore specifically to the removal of halogens from oils pr pared by condensation means.
- Our-invention will be fully understood from the following description and the example which illustrates one method of application of our process.
- the temperature range given above is preferred in order to obtain the most complete reaction within a reasonably short time, say less than five or ten hours.
- the temperature may also beabove 450 F. even up to 600 F. or slightly higher, but it is preferably below such temperatureas causes appreciable thermal decomposition of the oil.
- a hard parafiin wax having a melting point of 122 to 125 F. is chlorinatedv by the direction- The chlorine is blown through the oil for about 24 hours and after this time it is found that the product contains about 12% chlorine, although thereis some unchlorinated hydrocarbon.
- the heavy oil remaining has the following inspection:
- This synthetic oil and similar oils prepare'diby condensation of organic chlorides contains small amounts of residual chlorine whichis normally below 1% and may be as low as .2 to 0.05 of 1% and is objectionable. The majority of this chlorine may be removed by treatment with alumina,
- gasoline and alcohol are then removed by distillation using external heating and passing 3 steam through the liquid. No trace of chlorine is found in the final oil after this treatment.
- the oil is then suitable for use as a high quality lubricatingoil, or it may be blended with other oils suitable for lubrication, or it may be added in very small amounts of 10% to of 1% or less as a solidification inhibitor to oils of high pour point to produce a marked decrease in the pour point of the oil.
- oils prepared by synthetic means in which either organic or metallic halides are used the following are given; oils prepared by condensation of chloro-paraffin through the action of a high vacuum distillation,.
- Process for removing traces of halides from oils produced by condensation of organic material containing a halide comprising treating the liquid oil with a reactive metal in a liquid or molten condition at a temperature below the decomposition temperature of the oil.
- Process for removing traces of halides from lubricating oils produced by condensation of organic materials in the presence of metallic halides which comprises bringing the condensed liquid oil into contact at a temperature below 600 F. with the reactive metal in a molten condition.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Lubricants (AREA)
Description
Patented Nov. 7, 1933 UNITED STATES PROCESS FOR TREATING SYNTHETIC OILS Edward M. Jollyand Charles C. Swoope, Baton Rouge,La., assignors to Standard Oil Develop ment Company, a corporation of Delaware No Drawing. Application December 5, 1930 Serial No.- 500,424
"5 Claims] (o1. 196-23) The present invention relates to an improved method for treating lubricating oils andmore specifically to the removal of halogens from oils pr pared by condensation means. Our-invention will be fully understood from the following description and the example which illustrates one method of application of our process.
In the production of high grade lubricants, and in particular the lubricants prepared by condensation of organic halides or of organic materials in the presence of metallic halides, it is well known that the complete elimination of chlorine and other halogens from the finished product is necessary, particularly with motor oils or oils which are adapted for machinery operation at high temperatures. For example, a residue of as little as 0.1% chlorine is known to form combinations with iron and aluminum producing active cracking or polymerizing catalysts in the cylinders and bearings of the engine. The action of halogen is therefore undesirable both because of its corrosive effects on the engine parts and because of its catalytic effect in promoting the formation of carbon and sludge from the oil. We have now found a method whereby chlorine and similar substances may be removed from the lubricating oils so completelythat not even traces of residual chlorine may be found in the final oil. Our improved process consists essentially in treating the synthetic oil with reactive metal which is in a liquid condition under the conditions of operation In the operation of our process the condensed oil which has been found to contain traces of chlorine or other halides is subjected to the action of a reactive metal such as an alkali metal or mercury at a temperature of about 300 F. to 450 E, which is the preferred operating range. It will be understood that lower temperatures may be used which are ordinarily above the melting point of the particular metal say 210 F. for sodium for example, but usually the temperature range given above is preferred in order to obtain the most complete reaction within a reasonably short time, say less than five or ten hours. The temperature may also beabove 450 F. even up to 600 F. or slightly higher, but it is preferably below such temperatureas causes appreciable thermal decomposition of the oil.
As an example of the operation of. the process the following is given:.
A hard parafiin wax having a melting point of 122 to 125 F. is chlorinatedv by the direction- The chlorine is blown through the oil for about 24 hours and after this time it is found that the product contains about 12% chlorine, although thereis some unchlorinated hydrocarbon. To
90 parts of this chloro-paraffin 10 parts of naphkerosene and the unreacted paraffin as distillates.
The heavy oil remaining has the following inspection:
Gravity 23.4: A. P. I. Vis. at 100 F 8500 sec. Saybolt Vis. at 210 F 312 sec. Saybolt Pour 65 F.
Flash 535 F.
Conradson carbon 4.6% I
Residual chlorine .2%
This synthetic oil and similar oils prepare'diby condensation of organic chlorides contains small amounts of residual chlorine whichis normally below 1% and may be as low as .2 to 0.05 of 1% and is objectionable. The majority of this chlorine may be removed by treatment with alumina,
bauxite, and the like, but ordinary treatment with these agents does not remove all the chlo- ,rine and we have found that a final treatment with metals of the class described, namely those having melting points below 400 1 completely removes the residual chlorine. As an example of one method of treatment by our process the following is given:
500 grams of synthetic oil containing 0.02% chlorine is treated with 1 gram of sodium for four hours at 300-350 F. the mixture being stirred vigorously throughout this time with a mechanical stirrer. At the end of the four hours the mixture is allowed to cool and methyl alcohol is added to decompose the excess sodium. When reaction has ceased the oil is diluted with 300 cc.
of gasoline and washed well with hot water. The
gasoline and alcohol are then removed by distillation using external heating and passing 3 steam through the liquid. No trace of chlorine is found in the final oil after this treatment. The oil is then suitable for use as a high quality lubricatingoil, or it may be blended with other oils suitable for lubrication, or it may be added in very small amounts of 10% to of 1% or less as a solidification inhibitor to oils of high pour point to produce a marked decrease in the pour point of the oil.
While the above example shows the use of sodium for removing chlorine from a lubricating oil prepared by condensation of chloro-parafiin with a naphthenic compound in the presence of aluminum chloride it will be understood that our process includes the removal of halides from any.
lubricating oil prepared by synthetic means in which either organic or metallic halides are used. As examples of such oils the following are given; oils prepared by condensation of chloro-paraffin through the action of a high vacuum distillation,.
by the condensation of olefins and similar organic substances with metallic halides, or by the condensation of organic halides with oleflns or aromatic compounds. It will also be understood that other reactive metals having melting points below 400 F. including lithium, potassium, rubidium, caesium and mercury may be used in place of sodium. 7
This invention is not to be limited by any theory of the mechanism of the reactions nor to any specific example which may have been given for purpose of illustration, but only by the following claims in which it is wished to claim all novelty inherent in this invention.
We claim:
1. Process for removing traces of halides from oils produced by condensation of organic material containing a halide comprising treating the liquid oil with a reactive metal in a liquid or molten condition at a temperature below the decomposition temperature of the oil.
2. Process for removing traces of halides from lubricating oils produced by the condensation of organic halides by the action of metallic halides which comprises treatment of the condensed liquid oil at temperatures below about 600 F. with a metal which is in a molten condition at the temperature of treating.
,3. Process for removing traces of halides from lubricating oils produced by condensation of organic materials in the presence of metallic halides which comprises bringing the condensed liquid oil into contact at a temperature below 600 F. with the reactive metal in a molten condition.
4. Process according to claim 1 in which a metal from the class comprising alkali metals and mercury is used.
5. Process according to claim 1, in which sodium is used at a temperature between abou 190 and 450 F.
EDWARD M. JOLLY. CHARLES C. SWOOPE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US500424A US1934068A (en) | 1930-12-05 | 1930-12-05 | Process for treating synthetic oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US500424A US1934068A (en) | 1930-12-05 | 1930-12-05 | Process for treating synthetic oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1934068A true US1934068A (en) | 1933-11-07 |
Family
ID=23989356
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US500424A Expired - Lifetime US1934068A (en) | 1930-12-05 | 1930-12-05 | Process for treating synthetic oils |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1934068A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2463077A (en) * | 1943-08-30 | 1949-03-01 | Universal Oil Prod Co | Process for treating hydrocarbon mixtures to remove halogens therefrom |
| US2463076A (en) * | 1943-05-31 | 1949-03-01 | Universal Oil Prod Co | Treatment of hydrocarbons |
| US3097157A (en) * | 1960-06-10 | 1963-07-09 | Chilean Nitrate Sales Corp | Oil purification process |
| US4097369A (en) * | 1975-02-28 | 1978-06-27 | Adolf Schmids Erben Aktiengesellschaft | Process for reclaiming used hydrocarbon oils |
| US4255252A (en) * | 1978-03-25 | 1981-03-10 | Deutsche Gold Und Silber-Scheideanstalt Vormals Roessler | Procedure for the reprocessing of used lubricating oils |
| US4561969A (en) * | 1984-09-28 | 1985-12-31 | The United States Of America As Represented By The United States Department Of Energy | Method for removing chlorine compounds from hydrocarbon mixtures |
| WO2012038499A1 (en) | 2010-09-23 | 2012-03-29 | Shell Internationale Research Maatschappij B.V. | Process for reducing the halogen content of a hydrocarbon product stream by contacting with a metal |
-
1930
- 1930-12-05 US US500424A patent/US1934068A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2463076A (en) * | 1943-05-31 | 1949-03-01 | Universal Oil Prod Co | Treatment of hydrocarbons |
| US2463077A (en) * | 1943-08-30 | 1949-03-01 | Universal Oil Prod Co | Process for treating hydrocarbon mixtures to remove halogens therefrom |
| US3097157A (en) * | 1960-06-10 | 1963-07-09 | Chilean Nitrate Sales Corp | Oil purification process |
| US4097369A (en) * | 1975-02-28 | 1978-06-27 | Adolf Schmids Erben Aktiengesellschaft | Process for reclaiming used hydrocarbon oils |
| US4255252A (en) * | 1978-03-25 | 1981-03-10 | Deutsche Gold Und Silber-Scheideanstalt Vormals Roessler | Procedure for the reprocessing of used lubricating oils |
| US4561969A (en) * | 1984-09-28 | 1985-12-31 | The United States Of America As Represented By The United States Department Of Energy | Method for removing chlorine compounds from hydrocarbon mixtures |
| WO2012038499A1 (en) | 2010-09-23 | 2012-03-29 | Shell Internationale Research Maatschappij B.V. | Process for reducing the halogen content of a hydrocarbon product stream by contacting with a metal |
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