US1788204A - Process of bleaching mineral oils and fats - Google Patents
Process of bleaching mineral oils and fats Download PDFInfo
- Publication number
- US1788204A US1788204A US214214A US21421427A US1788204A US 1788204 A US1788204 A US 1788204A US 214214 A US214214 A US 214214A US 21421427 A US21421427 A US 21421427A US 1788204 A US1788204 A US 1788204A
- Authority
- US
- United States
- Prior art keywords
- bleaching
- oils
- mineral oils
- solution
- fats
- 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
- 238000004061 bleaching Methods 0.000 title description 36
- 239000002480 mineral oil Substances 0.000 title description 17
- 238000000034 method Methods 0.000 title description 16
- 235000014593 oils and fats Nutrition 0.000 title description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical class Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 42
- 239000003921 oil Substances 0.000 description 29
- 239000000243 solution Substances 0.000 description 24
- 150000003839 salts Chemical class 0.000 description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 11
- 239000000460 chlorine Substances 0.000 description 11
- 229910052801 chlorine Inorganic materials 0.000 description 11
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
- 238000000354 decomposition reaction Methods 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- 238000005406 washing Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 150000001805 chlorine compounds Chemical class 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 6
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910017052 cobalt Inorganic materials 0.000 description 5
- 239000010941 cobalt Substances 0.000 description 5
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- 239000003513 alkali Substances 0.000 description 4
- 238000009874 alkali refining Methods 0.000 description 4
- 229910001385 heavy metal Inorganic materials 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 2
- FAZNZOQAEBFDJI-UHFFFAOYSA-N (3,4a,5-trimethyl-9-oxo-4,5,6,7-tetrahydrobenzo[f][1]benzofuran-4-yl) acetate Chemical compound CC(=O)OC1C2(C)C(C)CCC=C2C(=O)C2=C1C(C)=CO2 FAZNZOQAEBFDJI-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 241000266847 Mephitidae Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- NWDGEEKPPUMFCN-UHFFFAOYSA-N [Ni++].[O-]Cl.[O-]Cl Chemical compound [Ni++].[O-]Cl.[O-]Cl NWDGEEKPPUMFCN-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229910000361 cobalt sulfate Inorganic materials 0.000 description 1
- 229940044175 cobalt sulfate Drugs 0.000 description 1
- KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 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
- C10G27/00—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation
- C10G27/02—Refining of hydrocarbon oils in the absence of hydrogen, by oxidation with halogen or compounds generating halogen; Hypochlorous acid or salts thereof
-
- 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
- C10G29/06—Metal salts, or metal salts deposited on a carrier
- C10G29/12—Halides
Definitions
- This invention relates to a method of bleaching mineral oils and fats and is more particularly concerned with the treatment of these substances for bleaching purposes after other, especially sulfur containing, impurities, such as the so-called skunk compound, have been removed, preferably by the known acid alkali treatment.
- hypochlorites substances which exert an accelerating action on the decomposition of hypochlorites into chloride and free oxygen, such as the salts of heavy metals, for instance, nickel, cobalt, copper &c, the bleach is easily initiated without the addition of an acid and a thorough utilization of the hypochlorite is brought about.
- substances which exert an accelerating action on the decomposition of hypochlorites into chloride and free oxygen such as the salts of heavy metals, for instance, nickel, cobalt, copper &c
- any means for removing the caustic alkali contents in the hypochlorite solution andserving to partially transform the hypochlorite to hypochlorous acid accelerates and enhances the accomplishment of the bleach.
- our process for bleaching any ordinary or prerefined mineral oil or fat-the latter in the liquid state at a correspondingly elevated temperature comprises a treatment with an aqueous hypochlorite solution in the presence of means for accelerating the decomposition of the hypochlorite .into its chloride and free oxygen, which means according to our invention consists in the simul- The nickel hypochlorite is immediately decomposed accordinging to the following equatron: I
- 0111 examples correspond only to single cases chosen at random and the exact proportions of the metal oxids, the concentration of the hypochlorite solution and "the addition of acidulating means must be ascertained in any special case by preliminary experiments, which however are easily performed.
- Examples 1 1000 kilograms of a mineral oil pre-refined by acids or alkalies in the well known manner-are mixed anduthoroughly stirred with kilograms of soda bleaching liquor containing 150 grams of available chlorine per liter. While stirring continually 500 grams of nickel sulfate dissolved in 50 liters of water are added. From time to time the available chlorine contents of a sample is tested. After the reaction is completed, which is indicated by the consumption of the available chlorine, the oil is heated to about C. to facilitate the separation of the emulsion and washed with water.
- 1000 kilograms of a distilled lubricating oil are at first treated with an acid and an alkali and then with a bleaching solution made in the following manner: 50 kilograms of soda bleaching liquor containing 150 grams of available chlorine per liter are mixed with 400 grams of cobalt sulfate dissolved in 50 liters of water and 2 kilograms of sodium bicarbonate dissolved in 20 liters of water. This bleaching solution is added to the mineral oil while stirring. During the bleaching operation stirring is continued. After consumption of the available chlorine the oil is further treated as described in the preceding example.
- the process of bleaching mineral oils which comprises subjecting said oils to a usual acid-alkali refining treatment, treat ing the refined oils with an aqueous hypochlorite solution in the presence of a salt of a metal selected from the group consisting of copper, nickel and cobalt, which salt is capable of accelerating the decomposition of hypochlorites into chlorides and oxygen, heating the resulting mixture to about 60 (1, separating the oils from the spent bleaching bath and washing said oils.
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)
- Detergent Compositions (AREA)
Description
Patented Jan, 6, 193B WILHELM POSTH AND FRANZ BESEMANN, OF BITTEBFELD, GERMANY, AS SIGNORS TO "1- USTBIE AKTIENGFSELLSGHAIFT, OI FRANKFORT-ON-THE-HAIN,
PROCESS OF BLEACHING MINERAL OILS FATS No Drawing. Application filed August 19, 1927, Serial No. 214,214, and in Germany July 21, 1926.
This invention relates to a method of bleaching mineral oils and fats and is more particularly concerned with the treatment of these substances for bleaching purposes after other, especially sulfur containing, impurities, such as the so-called skunk compound, have been removed, preferably by the known acid alkali treatment.
The products thus obtained frequently do not display the clearness generally required by the consumers and it has been already proposed to cure this by a treatment with hypochlorites. In this case, however, the difficulty arises that the bleaching liquor which acts but slowly in an alkaline solution is insufliciently utilized. On the other hand, when providing for the presence of a certain quantity of acid in the solution or considerably increasing the temperature, so as to prompt the formation of hypochlorous acid, secondary reactions of a detrimental nature are produced, these being soinetimes also followed by a subsequent darkening of the oil or fat.
Now we have found that by adding substances which exert an accelerating action on the decomposition of hypochlorites into chloride and free oxygen, such as the salts of heavy metals, for instance, nickel, cobalt, copper &c, the bleach is easily initiated without the addition of an acid and a thorough utilization of the hypochlorite is brought about.
Furthermore we have found that any means for removing the caustic alkali contents in the hypochlorite solution andserving to partially transform the hypochlorite to hypochlorous acid, as for instance a blCfl-I bona-te or other substance of weak acid character accelerates and enhances the accomplishment of the bleach.
Therefore our process for bleaching any ordinary or prerefined mineral oil or fat-the latter in the liquid state at a correspondingly elevated temperaturecomprises a treatment with an aqueous hypochlorite solution in the presence of means for accelerating the decomposition of the hypochlorite .into its chloride and free oxygen, which means according to our invention consists in the simul- The nickel hypochlorite is immediately decomposed acording to the following equatron: I
. Our improved process may be illustrated by the following examples. Taking into account the great variety and variability of materials to be treated it must be understood that within our general rule neither a speci fied rule as regards the composition of the bleaching solutions nor a schedule as regards the numerical proportions between bleaching goods and bleaching means can be given.
0111 examples correspond only to single cases chosen at random and the exact proportions of the metal oxids, the concentration of the hypochlorite solution and "the addition of acidulating means must be ascertained in any special case by preliminary experiments, which however are easily performed.
Examples 1. 1000 kilograms of a mineral oil pre-refined by acids or alkalies in the well known manner-are mixed anduthoroughly stirred with kilograms of soda bleaching liquor containing 150 grams of available chlorine per liter. While stirring continually 500 grams of nickel sulfate dissolved in 50 liters of water are added. From time to time the available chlorine contents of a sample is tested. After the reaction is completed, which is indicated by the consumption of the available chlorine, the oil is heated to about C. to facilitate the separation of the emulsion and washed with water.
2. 1000 kilograms of a distilled lubricating oil are at first treated with an acid and an alkali and then with a bleaching solution made in the following manner: 50 kilograms of soda bleaching liquor containing 150 grams of available chlorine per liter are mixed with 400 grams of cobalt sulfate dissolved in 50 liters of water and 2 kilograms of sodium bicarbonate dissolved in 20 liters of water. This bleaching solution is added to the mineral oil while stirring. During the bleaching operation stirring is continued. After consumption of the available chlorine the oil is further treated as described in the preceding example.
3. 1000 kilograms of paratfin are melted.
40 kilograms of a bleaching solution contain-,
ing about 150 grams of available chlorine per liter are diluted with an equal quantity of water and gradually added to the oil. Hereupon 150 grams of nickel sulfate dissolved in 2 liters of water are added and the reaction mixture is stirred while performing the bleaching action. As soon as no more active chlorine is ascertainable the oil is washed with hot water until neutral reaction is attained. The para-flin after being separated from the Water is allowed to solidify.
We claim 1. The process of bleaching pre-refined mineral oils which comprises treating them with an aqueous hypochlorite solution in the presence of a heavy metal salt capable of accelerating the decomposition of hypochlorites into chlorides and oxygen, heating the resulting mixture to about 60 C., separating the oils from the spent bleaching bath and washing said oils. i
2. The process of bleaching pro-refined mineral oils which comprises treating them with an aqueous hypochlorite solution in the presence of a salt of a metal selected from the group consisting of copper, nickel and cobalt, which salt is capable of accelerating the decomposition of hypochlorites into chlorides and oxygen, heating the resulting mixture to about 60 (3., separating the oils from the spent bleaching bath and washing said oils.
3. The process of bleaching pre-refiued mineral oils which comprises treating them with an aqueous hypochlorite solution in the presence of nickel sulfate, heating the resulting mixture to about 60 G, separating the oils from the spent bleaching bath and washing said oils.
4. The process of bleaching mineral Oils which comprises subjecting said oils to a usual acid-alkali refining treatment, treating the refined oils with an aqueous hypochlorite solution in the presence of a heavy metal salt capable of accelerating the decomposition of hypochloritesv into chlorides and oxygen, heating the resulting mixture to about 60 C.,
separating the oils from the spent bleaching bath and washing said oils.
5. The process of bleaching mineral oils which comprises subjecting said oils to a usual acid-alkali refining treatment, treat ing the refined oils with an aqueous hypochlorite solution in the presence of a salt of a metal selected from the group consisting of copper, nickel and cobalt, which salt is capable of accelerating the decomposition of hypochlorites into chlorides and oxygen, heating the resulting mixture to about 60 (1, separating the oils from the spent bleaching bath and washing said oils.
6. The process of bleaching mineral oils which comprises subjecting said oils to a usual acid-alkali refining treatment, treat-- ingthe refined oils with an aqueous hypochlorite solution in the presence of nickel sulfate, heating the resulting mixture to about 60 C., separating the oils from the spent bleaching bath and washing said oils.
7. The process of bleaching mineral oils which comprises subjecting said oils to a usual acid-alkali refining treatment, treating the refined oils with an aqueous alkaline hypochlorite solution containing a bicarbonate, whereby the alkalinity of the bleaching solution is reduced, in the presence of a salt of a metal selected from the group consisting of copper, nickel and cobalt, which salt is capable of accelerating the decompositin of hypochlorites into chlorides and oxygen, heating the resulting mixture to about 60 0., separating the oils from the spent bleaching bath and washing said oils.
8. The process of bleaching pre-refined mineral oils which comprises treating them with an aqueous hypochlorite solution, con-- taining about 150 grams of available chlorine per liter of solution, in the presence of a heavy metal salt capable of accelerating the decom-- position of hypochlorites into chlorides and oxygen.
9. The process of bleaching pre-refined mineral oils which comprises treating them with an aqueous hypochlorite solution, containing about 150 grams of available chlorine per liter of solution, in the presence of a salt of a metal selected from the group consisting of copper, nickel and cobalt, which salt is capable of accelerating the decomposition of hypochlorites into chlorides and oxygen.
10. The process of bleaching pro-refined mineral oils which comprises treating them with an aqueous hypochlorite solution, containing about 150 grams of available chlorine per liter of solution, in the presence of nickel sulfate.
11. The process of bleaching pre-refined mineral oils which comprises treating them with an aqueous hypochlorite solution, containing about 150 grams of available chlorine per liter of solution, in the. presence of nickel sulfate, heating the resulting mixture to about 60 (1, se arating the oils from the spent bleaching ath and washing said oils.
In testimony whereof we have hereunto set our hands.
wmLM POSTHI FRANZ BESEMANN.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1788204X | 1926-07-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1788204A true US1788204A (en) | 1931-01-06 |
Family
ID=7743335
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US214214A Expired - Lifetime US1788204A (en) | 1926-07-21 | 1927-08-19 | Process of bleaching mineral oils and fats |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1788204A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2755224A (en) * | 1952-12-18 | 1956-07-17 | Exxon Research Engineering Co | Process for improving lubricating oils |
| US4076762A (en) * | 1977-04-29 | 1978-02-28 | Engelhard Minerals & Chemicals Corporation | Continuous process for the removal of other hydrocarbons from saturated aliphatic hydrocarbons |
-
1927
- 1927-08-19 US US214214A patent/US1788204A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2755224A (en) * | 1952-12-18 | 1956-07-17 | Exxon Research Engineering Co | Process for improving lubricating oils |
| US4076762A (en) * | 1977-04-29 | 1978-02-28 | Engelhard Minerals & Chemicals Corporation | Continuous process for the removal of other hydrocarbons from saturated aliphatic hydrocarbons |
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