US2079782A - Process of deodorizing lubricating oils - Google Patents
Process of deodorizing lubricating oils Download PDFInfo
- Publication number
- US2079782A US2079782A US717541A US71754134A US2079782A US 2079782 A US2079782 A US 2079782A US 717541 A US717541 A US 717541A US 71754134 A US71754134 A US 71754134A US 2079782 A US2079782 A US 2079782A
- Authority
- US
- United States
- Prior art keywords
- oil
- lubricating oils
- deodorizing
- odor
- steam
- 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
- 239000010687 lubricating oil Substances 0.000 title description 5
- 238000000034 method Methods 0.000 title description 5
- 230000001877 deodorizing effect Effects 0.000 title description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 26
- 239000003921 oil Substances 0.000 description 19
- 235000019645 odor Nutrition 0.000 description 11
- 239000004927 clay Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 3
- IXWIAFSBWGYQOE-UHFFFAOYSA-M aluminum;magnesium;oxygen(2-);silicon(4+);hydroxide;tetrahydrate Chemical compound O.O.O.O.[OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Mg+2].[Al+3].[Si+4].[Si+4].[Si+4].[Si+4] IXWIAFSBWGYQOE-UHFFFAOYSA-M 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000010727 cylinder oil Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000005325 percolation Methods 0.000 description 2
- 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 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical class [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- -1 for example Chemical class 0.000 description 1
- 229910000286 fullers earth Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C10G17/00—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge
- C10G17/08—Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge with acid-forming oxides
-
- 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 a process of producing lubricating oils of improved odor and will be understood from the following description when read in conjunction with the drawing the sole figure of which is a diagrammatic side elevation partly in section of an apparatus appropriate for carrying out the invention.
- Lubricating oils which have been treated with an adsorbent clay often develop a disagreeable odor. This is especially the case with lubricating oils and cylinder stocks which have been nished by percolation through coarse clay such as coarse fullers earth or Attapulgus clay. Such percolation is often carried out at temperatures ranging from 200-350 F. and higher. It is believed that this odor is caused by the action of the clay on the sulphur compounds, thereby forming I-IzS and similar compounds.
- I have found that the treatment of these oils with a small quantity of SO2 in the presence of moisture will destroy this odor.
- the necessary time of treating can be shortened by raising the temperature to from 100 F. to 200 F. and above. A treating temperature of 150 F. very often gives good practical results. Any small excess of SO2 can readily be removed by blowing with steam, air, inert gas, such as naturalgas, refinery gas, nitrogen, CO2, etc., which at the same time brightens the oil due to the removal of the water vapors
- any compound such as, for example, sodium or potassium bi-sulphite, which contains a loosely bound SO2 group can be used.
- the lubricating oil from storage tank I is pumped through preheater 2 and percolatng filter tank 3.
- the tank is filled with coarse clay 4 and provided with 4U lagging 5 to prevent heat losses.
- the treated oil is then passed through heating or cooling coil 6 to adjust its temperature and is pumped into the deodorizing tank l.
- sodium bi-sulphite solution When sodium bi-sulphite solution is used, the same may be pumped from the storage tank (not shown) through line 3 directly into the oil line leaving coil 6.
- Tank l is also provided with lagging 9 to prevent heat loss and with a ⁇ steam or inert gas line I0 conm nected with line Il for the introduction of SO2.
- lubricating cil is meant to designate both lubricating oils and cylinder oils, whether obtained by overhead distillation or as residual stocks.
- An improved process for refining mineral lubricating oils and removing objectionable odors therefrom comprising the separate steps of treating the oil with clay at a temperature of the order of 200 F. and higher, separating the clay and then agitating the oil with moist sulfur dioxide at A a temperature below 200 F. and then removing any excess thereof.
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)
- Fats And Perfumes (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Lubricants (AREA)
Description
May l1, 1937. A. A. WELLS POCESS OF DEODORIZING LUBRICATING OILS Filed March 27, 1934 Ill QQ @NSW l s URN Patented May 11, 1937 UNITED srargs PROCESS F DEODORIZING LUBRICATING OILS Alfred A. Wells, Roselle Park, N. J., assignor t0 Standard Oil Development Company, a corporation of Delaware Application March 27,4
2 Claims.
This invention relates to a process of producing lubricating oils of improved odor and will be understood from the following description when read in conjunction with the drawing the sole figure of which is a diagrammatic side elevation partly in section of an apparatus appropriate for carrying out the invention.
Lubricating oils which have been treated with an adsorbent clay often develop a disagreeable odor. This is especially the case with lubricating oils and cylinder stocks which have been nished by percolation through coarse clay such as coarse fullers earth or Attapulgus clay. Such percolation is often carried out at temperatures ranging from 200-350 F. and higher. It is believed that this odor is caused by the action of the clay on the sulphur compounds, thereby forming I-IzS and similar compounds. I have found that the treatment of these oils with a small quantity of SO2 in the presence of moisture will destroy this odor. The necessary time of treating can be shortened by raising the temperature to from 100 F. to 200 F. and above. A treating temperature of 150 F. very often gives good practical results. Any small excess of SO2 can readily be removed by blowing with steam, air, inert gas, such as naturalgas, refinery gas, nitrogen, CO2, etc., which at the same time brightens the oil due to the removal of the water vapors present.
Instead of using SO2 gas, any compound such as, for example, sodium or potassium bi-sulphite, which contains a loosely bound SO2 group can be used.
Referring now to the drawing, the same will be 5 described in conjunction with the method of operating the apparatus shown. The lubricating oil from storage tank I is pumped through preheater 2 and percolatng filter tank 3. The tank is filled with coarse clay 4 and provided with 4U lagging 5 to prevent heat losses. The treated oil is then passed through heating or cooling coil 6 to adjust its temperature and is pumped into the deodorizing tank l. When sodium bi-sulphite solution is used, the same may be pumped from the storage tank (not shown) through line 3 directly into the oil line leaving coil 6. Tank l is also provided with lagging 9 to prevent heat loss and with a` steam or inert gas line I0 conm nected with line Il for the introduction of SO2. UU The steam and SO2 are discharged into tank 'i through the spray i2. The treated oil is removed through bottom line I3, cooler I4 into the finished oil tank i5. The steam and gas leave tank i through overhead line It and steam condenser I1. A receiver l0 for any condensate, vent line l0 and vacuum pump are provided as shown.
The following examples will illustrate my invention: A cylinder oil which had been acid 1934, serial No. 717,541
treated and neutralized in the ordinary way was percolated through Attapulgus clay at a temperature of Z50-300 F. The oil coming from the percclating unit was cooled to 150 F. and then blown with steam for a short period. SO2 gas was then bubbled into the oil until a slight odor of SO2 could be detected. The SO2 supply was then shut 01T and the oil blown with air at 150 F. until the odor of SO2 had disappeared. The disagreeable odor of the original percolatecl oil was largely removed.
In another experiment the sample of oil which had previously been percolated at a temperature above 250 F. and which had a disagreeable odor was heated to 150 F. while at the same time a small amount of steam was blown through the oil. A solution or" sodium bi-sulphite was then added to the oil in the ratio of 0.35 gram of sodium bi-sulphite to a liter of oil and agitated with air for a brief period. The oil was then blown with steam at approximately 150 F. until the odor of sodium bi-sulphite had disappeared. The resulting oil was sweet in odor.
Still in another experiment the sample of oil which had been treated with SO2, as in the iirst example, was blown with nitrogen under a slight vacuum at a temperature of 200 F. to remove the traces of SO2. This sample had a particularly good odor.
In the following claims the term lubricating cil is meant to designate both lubricating oils and cylinder oils, whether obtained by overhead distillation or as residual stocks.
My process may be modified in various ways. The blowing with air or steam or inert gas may be carried out in atmospheric pressure or under vacuum. Other changes and modiications will be apparent to those skilled in the art. Therefore, my invention is not to be limited by the examples given ior illustration but only by the following claims, in which it is my intention to claim all novelty inherent in the invention.
What I claim is:
l. An improved process for refining mineral lubricating oils and removing objectionable odors therefrom, comprising the separate steps of treating the oil with clay at a temperature of the order of 200 F. and higher, separating the clay and then agitating the oil with moist sulfur dioxide at A a temperature below 200 F. and then removing any excess thereof.
2. A process according to claim 1 in which the clay treating step is accomplished at a temperature within the range from about 200 to 350 F., and treatment with moist sulfur dioxide at a lower temperature range within from about 100 to 200 F.
ALFRED A. WELLS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US717541A US2079782A (en) | 1934-03-27 | 1934-03-27 | Process of deodorizing lubricating oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US717541A US2079782A (en) | 1934-03-27 | 1934-03-27 | Process of deodorizing lubricating oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2079782A true US2079782A (en) | 1937-05-11 |
Family
ID=24882438
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US717541A Expired - Lifetime US2079782A (en) | 1934-03-27 | 1934-03-27 | Process of deodorizing lubricating oils |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2079782A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2498201A (en) * | 1947-02-12 | 1950-02-21 | Socony Vacuum Oil Co Inc | Deodorizing refined petroleum oils and waxes |
| US2773861A (en) * | 1955-12-30 | 1956-12-11 | Standard Oil Co | Process of stabilizing phosphorus sulfide-oxygen containing organic compound reaction products against hydrogen sulfide evolution |
| US2773862A (en) * | 1955-12-30 | 1956-12-11 | Standard Oil Co | Process of stabilizing phosphorus sulfide-oxygen-containing organic compound reaction products |
| US2773860A (en) * | 1955-12-30 | 1956-12-11 | Standard Oil Co | Process of stabilizing phosphorus sulfide-oxygen-containing organic compound reaction products against liberation of hydrogen sulfide |
| US3876534A (en) * | 1971-12-23 | 1975-04-08 | Ballestra Spa | Method for the removal of non-saturated and/or aromatic hydrocarbons from saturated paraffin hydrocarbons and a device to embody said method |
| US4332676A (en) * | 1980-12-19 | 1982-06-01 | Exxon Research & Engineering Co. | Removal of basic nitrogen compounds from organic streams |
| US4332675A (en) * | 1980-12-19 | 1982-06-01 | Exxon Research & Engineering Co. | Removal of basic nitrogen compounds from organic streams |
-
1934
- 1934-03-27 US US717541A patent/US2079782A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2498201A (en) * | 1947-02-12 | 1950-02-21 | Socony Vacuum Oil Co Inc | Deodorizing refined petroleum oils and waxes |
| US2773861A (en) * | 1955-12-30 | 1956-12-11 | Standard Oil Co | Process of stabilizing phosphorus sulfide-oxygen containing organic compound reaction products against hydrogen sulfide evolution |
| US2773862A (en) * | 1955-12-30 | 1956-12-11 | Standard Oil Co | Process of stabilizing phosphorus sulfide-oxygen-containing organic compound reaction products |
| US2773860A (en) * | 1955-12-30 | 1956-12-11 | Standard Oil Co | Process of stabilizing phosphorus sulfide-oxygen-containing organic compound reaction products against liberation of hydrogen sulfide |
| US3876534A (en) * | 1971-12-23 | 1975-04-08 | Ballestra Spa | Method for the removal of non-saturated and/or aromatic hydrocarbons from saturated paraffin hydrocarbons and a device to embody said method |
| US4332676A (en) * | 1980-12-19 | 1982-06-01 | Exxon Research & Engineering Co. | Removal of basic nitrogen compounds from organic streams |
| US4332675A (en) * | 1980-12-19 | 1982-06-01 | Exxon Research & Engineering Co. | Removal of basic nitrogen compounds from organic streams |
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