US1990490A - Method of producing insecticide and the like - Google Patents
Method of producing insecticide and the like Download PDFInfo
- Publication number
- US1990490A US1990490A US547788A US54778831A US1990490A US 1990490 A US1990490 A US 1990490A US 547788 A US547788 A US 547788A US 54778831 A US54778831 A US 54778831A US 1990490 A US1990490 A US 1990490A
- Authority
- US
- United States
- Prior art keywords
- shale oil
- water
- miscible
- oil
- shale
- 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
- 238000000034 method Methods 0.000 title description 14
- 239000002917 insecticide Substances 0.000 title description 4
- 239000003079 shale oil Substances 0.000 description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 35
- 239000000203 mixture Substances 0.000 description 14
- 239000000047 product Substances 0.000 description 12
- 239000000463 material Substances 0.000 description 10
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- 239000003513 alkali Substances 0.000 description 8
- 238000009877 rendering Methods 0.000 description 8
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 7
- 239000005642 Oleic acid Substances 0.000 description 7
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 7
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 239000000344 soap Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 4
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 235000011118 potassium hydroxide Nutrition 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- -1 sutidine Natural products 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- 241000118205 Ovicides Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 230000002070 germicidal effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000011837 pasties Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 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
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- HOPRXXXSABQWAV-UHFFFAOYSA-N anhydrous collidine Natural products CC1=CC=NC(C)=C1C HOPRXXXSABQWAV-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-O azanium;hydron;hydroxide Chemical compound [NH4+].O VHUUQVKOLVNVRT-UHFFFAOYSA-O 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- UTBIMNXEDGNJFE-UHFFFAOYSA-N collidine Natural products CC1=CC=C(C)C(C)=N1 UTBIMNXEDGNJFE-UHFFFAOYSA-N 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000320 mechanical mixture Substances 0.000 description 1
- 125000005608 naphthenic acid group Chemical group 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000004058 oil shale Substances 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 150000007965 phenolic acids Chemical class 0.000 description 1
- 235000009048 phenolic acids Nutrition 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- LTUDISCZKZHRMJ-UHFFFAOYSA-N potassium;hydrate Chemical group O.[K] LTUDISCZKZHRMJ-UHFFFAOYSA-N 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 150000003388 sodium compounds Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000002557 soporific effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/924—Significant dispersive or manipulative operation or step in making or stabilizing colloid system
- Y10S516/927—Significant dispersive or manipulative operation or step in making or stabilizing colloid system in situ formation of a colloid system making or stabilizing agent which chemical reaction
Definitions
- the principal object of the invention is to take advantage of the toxicvalue of shale oil for such purposes.
- Another important object of the invention is to provide such a product that is an oily liquid that will be readily miscible with hot or cold water.
- the material is usually mixed with water in the orchard, vineyard, or other place where it is to be used. It isimpractical to have to mix the toxic material with water under heat.
- a further object is to provide a material for the purpose stated that will contain a relatively large amountof the toxic shale oil (preferably more than eighty-five per cent) and a relatively 1 small amount of material to render the oil miscible with water (less than fifteen per cent).
- Another object of the invention consists in taking advantage of the alkaline constituentsnaturally present in shale oil, such as naphthaline, secondary amines such as diethylamine, tertiary amine such, as triethylamine, sutidine, collidine ysis of these compounds in the presence of heat with a fatty acid, such as oleic acid, renders the oily alkaline constituents of shale oil miscible with water.
- a fatty acid such as oleic acid
- Our process consists principally in treating a shale oil product, such as pressure distillate of shale oil, from which the shale oil gasoline has been removed, and has a Baum gravity of, for [0 example, thirty-four degrees to forty-two degrees, with a small percentage (two per cent to five percent ,is preferable) of unsaturated fatty acid such as oleic acid. To the foregoing is added a small amount (one per cent to one and one-half per cent) of an alkalijsuch as potassium hydrate in solution. It is important not to mix the reagents together before mixing same with oil, for a different reaction results.
- reaction which takes place between a portion of the oleic acid and the excess of potassium hydrate forms a compound which parting from with water.
- alkalis such as sodium or ammonium hydrate.
- an alkali wash resulting from refining shale oil products may be used.
- Such washes contain salts of naphthenic acid phenolic acid and cresolic acid.
- condenser water resulting from retorting oil shale may be used.
- Pressure distillate of shale oil treated by one of the foregoing processes, has desirable proper-' ties as an insecticide, germicide, ovicide, and fungicide, but will not burn foliage of plants when sufficiently'diluted, and is thoroughly misciblewith water. As stated, an emulsion appreaching a perfect emulsion is obtained on dilution with water.
- alkali-containing material includes Potassium and sodium compounds and ammonium compounds.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented Feb. 12, 1935 1,990,490 METHOD OF PRODUCING INSECTICIDE AND THE LIKE Joseph W.-Horne and Carl P. Hopkins,
- Boulder, C010.
No llrawing. Application June Serial No. 547,788
8 Claims. (01. 167-28) Our invention relates to insecticides, germicides,
fungicides, ovicides, and the like. The principal object of the invention is to take advantage of the toxicvalue of shale oil for such purposes.
Another important object of the invention is to provide such a product that is an oily liquid that will be readily miscible with hot or cold water.
In practice, the material is usually mixed with water in the orchard, vineyard, or other place where it is to be used. It isimpractical to have to mix the toxic material with water under heat.
A further object is to provide a material for the purpose stated that will contain a relatively large amountof the toxic shale oil (preferably more than eighty-five per cent) and a relatively 1 small amount of material to render the oil miscible with water (less than fifteen per cent).
Heretofore experiments have .been made to make an emulsion of the oil and water by the use of a mechanical mixture with soap. The difliculty has been that a relatively large amount (approximately fifty per cent) of such reagent had to be used to make such an emulsion. The result was a soapy mass in a pasty condition. Of course, it is much more preferable to use as little reagent as possible, for otherwise it dilutes the toxic shale oil too much.
However, the shale oil must undergo some treatment in order to render it miscible with water and especially with cold water. Untreated shale oil will rise to the top of water in a. very short time,
as in the case of any oil, but after being treated and higher compounds in the series, and the pyrolin taking advantage of the 'acid reacting constituents naturally present in shale oil, such as naphthenes, phenols and cresols and the hydrolysis of these compounds in the presence of an alkali with heat, rendering the acid reacting constituents of shale oil miscible with water.
Another object of the invention consists in taking advantage of the alkaline constituentsnaturally present in shale oil, such as naphthaline, secondary amines such as diethylamine, tertiary amine such, as triethylamine, sutidine, collidine ysis of these compounds in the presence of heat with a fatty acid, such as oleic acid, renders the oily alkaline constituents of shale oil miscible with water. 1 Other objects reside in details of the invention, in the materials used to treat the shale oil and in the proportions thereof, which will appear in the 5 course of the following detailed description,
Our process consists principally in treating a shale oil product, such as pressure distillate of shale oil, from which the shale oil gasoline has been removed, and has a Baum gravity of, for [0 example, thirty-four degrees to forty-two degrees, with a small percentage (two per cent to five percent ,is preferable) of unsaturated fatty acid such as oleic acid. To the foregoing is addeda small amount (one per cent to one and one-half per cent) of an alkalijsuch as potassium hydrate in solution. It is important not to mix the reagents together before mixing same with oil, for a different reaction results.
The combining is dofieunder heat and the ing'redients are continuously agitated and heated for approximately an. hour. Hydrolysis of a portion of the shale oiltakes place by means of a series of chemical reactions, such as-the following:
.CHz-CHa' n CH:\ /C I I +Hydrolysls+ QHz-CH: COiCH: N 033011 ron carom H CHz-GHi 002K Reactions similar to this occur between the natural naphthenic acids and related compounds present in the shale oil products in the presence of an active alkali, the presence of which render the shale oil product partially miscible. The soporific and miscible qualities are improved and completed by the reactions between the unsaturated fatty acid and the active alkali, which are separately added. Salts so formed in the above process are soluble in the phenolic acids and cresolic acids naturally present in the shale oil used and aid in forming a homogenous liquid of the finished product. v
It is readily apparent from the material when the reactions have taken place, because the properties of the oil are changed; viz., the viscosity of the oil has been increased by the formation of new and/or other compounds; and the oil isnow miscible with water.
Moreover, the reaction which takes place between a portion of the oleic acid and the excess of potassium hydrate forms a compound which parting from with water.
of shale oil miscible'with water,
products resulting from water used to wash the concentrated sulphuric acid sludge recovered from refining shale oil products may be used. When this partial substitution is made, it is preferred to use about ten per cent of the sulpho-l nated products, in which case, one per cent of the oleic acid is dispensed with. All of these compounds neutralize the nitrogenous compounds of the shale oil distillate.
'In'place of the potassium hydrate, other alkalis may be used, such as sodium or ammonium hydrate. Instead of one of said alkalis, an alkali wash resulting from refining shale oil products may be used. Such washes contain salts of naphthenic acid phenolic acid and cresolic acid. In lieu of or in addition to such washes, condenser water resulting from retorting oil shale may be used.
Pressure distillate of shale oil, treated by one of the foregoing processes, has desirable proper-' ties as an insecticide, germicide, ovicide, and fungicide, but will not burn foliage of plants when sufficiently'diluted, and is thoroughly misciblewith water. As stated, an emulsion appreaching a perfect emulsion is obtained on dilution with water.
-As further proof that a chemical change has taken place in the shale oil when treated by the foregoing process, a mixture of untreated shale oil and water does not change thecolor of the oil, even though violently agitated. In a mixture of water and pressure distillate of shale oil, treated in accordance with the foregoing process, the oil turns a very light tan orcream colorquite unlike the dark brown color of the. original, untreated shale oil.
Any user can mix the present product and water anywhere by just pouring the two together and stirring. With a pasty mass, which was obtained in the prior art, the water must be heated and the agitation must continue until the'paste is thoroughly dissolved. It is usually quite impractical for the ordinary user to. heat the water,, so the advantages of the present product are thought apparent.
An important feature of the invention the hydrolysis of the natural constituents of shale oil and the addition of certain reagents to produce changes in the oil which renders the oil miscible It is to be understood that changes may be madein the invention, as by the use of equivalents for the above ingredients, and that changes may be made in proportions thereof, without dethe spirit and scope ofithe invention. The term alkali-containing material as used in the claims includes Potassium and sodium compounds and ammonium compounds.
What we claim and desire to secure by Letters Patent is:
1. The process of rendering a pressure distillate comprising first to form a soap, whereby the final composition is rendered miscible with hot or cold water. I
3. The process of rendering a shale oil distillate misciblewith water, comprising chemically combining said shale oil distillate with an unsaturated fatty acid, and then treating the resulting reaction product with sufiicient base in the preswhereby the final cold ence of heat to form a soap, composition is rendered miscible with hot or water.
4. The process of rendering a shale oil distillate miscible with water, comprising chemically combining said shale oil with oleic acid, allowing the mixture to react, and then adding sufficient alka- Ii-cQntaining material to the reaction product in the presence of heat to form a soap, whereby the final composition is. rendered miscible with hot or cold water.
5. The process of rendering a shale oil distillate miscible with water, comprising chemically combining said shale oil with an unsaturated fatty acid, allowing the mixture to react, and then adding sufiicient alkali-containing material to the reaction product in the presence of heat to form a soap, whereby the finalcomposition is rendered miscible with hot or cold water.
6. The process of rendering a shale oil distillate miscible with water, comprising chemically combining said shale oil distillate with oleic acid in an amount varying between 2% and 5%, allowing-the mixture to react, and then adding about 1% of an alkali-containing material to the reaction product in the presence of heat, whereby the final composition is rendered miscible with hot or cold water.
'7. The process of rendering a shale oil distillate miscible with water, comprising chemically combining said shale oil distillate with oleic acid in an amount varying between 2% and 5%, al lowing the mixture to react, and then adding about 1% of potassium hydrate to the reaction product in the presence of heat, whereby the final composition is rendered miscible with hot or cold water.
8. The process of rendering a shale oil distillate miscible with water, comprising chemically rived from the treatment of sulphuric acid sludge recovered from refining shale oil, allowing the latter mixture to react with the shale oil, and then adding-suf icient to the reaction product in the presence of heat to form a soap, whereby the final composition is ren dered miscible with hot or cold water.
.iosEPn w. HORNE. CARL P. norms.
alkali-containing product
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US547788A US1990490A (en) | 1931-06-29 | 1931-06-29 | Method of producing insecticide and the like |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US547788A US1990490A (en) | 1931-06-29 | 1931-06-29 | Method of producing insecticide and the like |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1990490A true US1990490A (en) | 1935-02-12 |
Family
ID=24186129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US547788A Expired - Lifetime US1990490A (en) | 1931-06-29 | 1931-06-29 | Method of producing insecticide and the like |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1990490A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2708185A (en) * | 1948-09-15 | 1955-05-10 | Scottish Oils Ltd | Detergent compositions |
-
1931
- 1931-06-29 US US547788A patent/US1990490A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2708185A (en) * | 1948-09-15 | 1955-05-10 | Scottish Oils Ltd | Detergent compositions |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1151795B (en) | Process for making low salt alkyl glyceryl ether sulfonates | |
| US1990490A (en) | Method of producing insecticide and the like | |
| US2243519A (en) | Asphalt emulsion and method of preparing same | |
| US1643675A (en) | Bituminous emulsion | |
| DE582790C (en) | Process for the production of cleaning, emulsifying and wetting agents | |
| DE670096C (en) | Process for the production of pellets from protein substances and / or protein breakdown products | |
| DE728224C (en) | Process for the preparation of derivatives of the condensation products from high molecular weight protein breakdown products and higher molecular weight saturated or unsaturated fatty acids | |
| DE868952C (en) | laundry detergent | |
| US1790070A (en) | Process for the manufacture of concentrated emulsions of oil and water | |
| US1939169A (en) | Method of preparing an aluminum sulphostearate | |
| DE622262C (en) | Process for the production of sulfuric acid esters from linseed oil and similar drying oils | |
| US1840157A (en) | Manufacture of new products comprising lignone derivatives | |
| US2116884A (en) | Manufacture of lead-manganese | |
| US2128247A (en) | L i ed blailb faient office | |
| DE504693C (en) | Process for the production of disinfecting substances | |
| DE652959C (en) | Process for obtaining a product containing organic nitrogen bases from acid sludge | |
| US2006895A (en) | Insecticides and fungicides and process of making the same | |
| US1502956A (en) | Insecticide | |
| US286048A (en) | William j | |
| US2017391A (en) | Insecticidal and fungicidal composition | |
| US2144260A (en) | Method of preparing an emulsifiable oil | |
| DE875652C (en) | Process for the production of a product suitable as an antioxidant for mineral oils and mixtures containing mineral oils | |
| US1867778A (en) | Process of producing sulphonic acids and sulphonates | |
| US1817120A (en) | Fur treating composition and process of making same | |
| DE555311C (en) | Process for the production of wetting and emulsifying agents |