GB506678A - Improvements in the manufacture and production of products similar to wax or petroleum jelly - Google Patents
Improvements in the manufacture and production of products similar to wax or petroleum jellyInfo
- Publication number
- GB506678A GB506678A GB3410637A GB3410637A GB506678A GB 506678 A GB506678 A GB 506678A GB 3410637 A GB3410637 A GB 3410637A GB 3410637 A GB3410637 A GB 3410637A GB 506678 A GB506678 A GB 506678A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fatty acids
- products
- distillation
- hydrogen
- residue
- 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
Links
- 235000019271 petrolatum Nutrition 0.000 title abstract 6
- 238000004519 manufacturing process Methods 0.000 title 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 8
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 5
- 238000004821 distillation Methods 0.000 abstract 5
- 239000000194 fatty acid Substances 0.000 abstract 5
- 229930195729 fatty acid Natural products 0.000 abstract 5
- 150000004665 fatty acids Chemical class 0.000 abstract 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 150000002576 ketones Chemical class 0.000 abstract 4
- 239000003921 oil Substances 0.000 abstract 4
- 230000003647 oxidation Effects 0.000 abstract 4
- 238000007254 oxidation reaction Methods 0.000 abstract 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 3
- 150000001298 alcohols Chemical class 0.000 abstract 3
- 238000005984 hydrogenation reaction Methods 0.000 abstract 3
- 229910052742 iron Inorganic materials 0.000 abstract 3
- 239000012188 paraffin wax Substances 0.000 abstract 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical class [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 2
- 244000068988 Glycine max Species 0.000 abstract 2
- 235000010469 Glycine max Nutrition 0.000 abstract 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 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- 239000001993 wax Substances 0.000 abstract 2
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 abstract 1
- 235000013162 Cocos nucifera Nutrition 0.000 abstract 1
- 244000060011 Cocos nucifera Species 0.000 abstract 1
- 235000010919 Copernicia prunifera Nutrition 0.000 abstract 1
- 244000180278 Copernicia prunifera Species 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 240000006240 Linum usitatissimum Species 0.000 abstract 1
- 235000004431 Linum usitatissimum Nutrition 0.000 abstract 1
- 235000004443 Ricinus communis Nutrition 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 235000015278 beef Nutrition 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 229910002091 carbon monoxide Inorganic materials 0.000 abstract 1
- 229910002090 carbon oxide Inorganic materials 0.000 abstract 1
- 239000004203 carnauba wax Substances 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 229910017052 cobalt Inorganic materials 0.000 abstract 1
- 239000010941 cobalt Substances 0.000 abstract 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 1
- 230000000911 decarboxylating effect Effects 0.000 abstract 1
- 238000006114 decarboxylation reaction Methods 0.000 abstract 1
- 239000003925 fat Substances 0.000 abstract 1
- 235000004426 flaxseed Nutrition 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 230000000266 injurious effect Effects 0.000 abstract 1
- 239000003077 lignite Substances 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000012170 montan wax Substances 0.000 abstract 1
- 229910000480 nickel oxide Inorganic materials 0.000 abstract 1
- 239000002674 ointment Substances 0.000 abstract 1
- 238000007127 saponification reaction Methods 0.000 abstract 1
- XCUPBHGRVHYPQC-UHFFFAOYSA-N sulfanylidenetungsten Chemical compound [W]=S XCUPBHGRVHYPQC-UHFFFAOYSA-N 0.000 abstract 1
- 239000003760 tallow Substances 0.000 abstract 1
- 239000011269 tar Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000010698 whale oil Substances 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 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
- C10G73/00—Recovery or refining of mineral waxes, e.g. montan wax
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
Abstract
506,678. Hydrocarbons; alcohols; ketones. JOHNSON, G. W. (I. G. Farbenindustrie.Akt.-Ges.) Dec. 9, 1937, No. 34106. [Class 2 (iii)] Products resembling wax or petroleum jelly arc obtained by heating distillation residues of high molecular weight fatty acids with decarboxylating catalysts, and reducing the products with hydrogen. Residues obtained by distillation of fatty acids. from the saponification of natural oils, fats or waxes, e.g. coconut, pahn kernel, castor, linseed, soya bean, and train oils, beef tallow, carnauba and montan waxes or from the oxidation of paraffins or hydrogenation products of coals, tars, and carbon oxides may be treated, in particular those obtained by distillation under reduced pressure, if desired while leading in, for example, steam, water, benzine or benzene, as described in Specification 213,267, [Class 32]. The residues may first be purified as by hydrogenation. Waxy, oily or fatty substances may be added before or during the working up. Metallic iron or nickel or manganese oxide or even the walls of metallic reaction vessels may be used as catalysts for the decarboxylation, generally at above 200‹ C. Increased pressure may be used. The treatment is generally continued until evolution of carbon dioxide ceases, the product then consisting of ketones. The subsequent reduction may be effected with hydrogen at, 10-250 atmos. and 100-500‹ C., in thepresence of catalysts such as metallic nickel, cobalt or iron or tungsten sulphide, preferably on carriers, or with zinc and acid or sodium and alcohol. It may be interrupted when part of the ketones is still present as such or as alcohols. The products are mainly hydrocarbons and/or alcohols of high molecular weight. They may be used in oil pastes, for protecting metals and other substances from injurious gases or, when fully hydrogenated, as bases for salves. In examples: (1) and (2) the residue from the distillation according to Specification 213,267 of fatty acids obtained from soya bean oil is hydrogenated, decarboxylated by heating with iron powder, and then hydrogenated to products resembling ozokerite or petroleum jelly ; (3) fatty acids made by oxidation of paraffin wax synthesized from carbon monoxide and hydrogen are distilled with steam under reduced pressure, and the residue similarly treated ; (4), (5), (6) the residue after distilling crude fatty acids obtained by oxidation of brown coal paraffin wax is heated with iron powder to give a ketone mixture. This is hydrogenated alone or after mixing with refrigerator oil, or, is dissolved in butyl alcohol and reduced by adding sodium ; (7) the distillation residue of the oxidation product of synthetic paraffin wax is heated with iron, and reduced with hydrogen. Further hydrogenation with fresh catalyst removes the colour.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3410637A GB506678A (en) | 1937-12-09 | 1937-12-09 | Improvements in the manufacture and production of products similar to wax or petroleum jelly |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3410637A GB506678A (en) | 1937-12-09 | 1937-12-09 | Improvements in the manufacture and production of products similar to wax or petroleum jelly |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB506678A true GB506678A (en) | 1939-06-02 |
Family
ID=10361442
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3410637A Expired GB506678A (en) | 1937-12-09 | 1937-12-09 | Improvements in the manufacture and production of products similar to wax or petroleum jelly |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB506678A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008157465A3 (en) * | 2007-06-15 | 2009-11-19 | E. I. Du Pont De Nemours And Company | Catalytic process for converting renewable resources into paraffins for use as diesel blending stocks |
-
1937
- 1937-12-09 GB GB3410637A patent/GB506678A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008157465A3 (en) * | 2007-06-15 | 2009-11-19 | E. I. Du Pont De Nemours And Company | Catalytic process for converting renewable resources into paraffins for use as diesel blending stocks |
| EP2540804A1 (en) * | 2007-06-15 | 2013-01-02 | E. I. du Pont de Nemours and Company | Catalytic process for converting renewable resources into paraffins for use as diesel blending stocks |
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