US1558880A - Solvent and vehicle for resinous and gelatinized material - Google Patents
Solvent and vehicle for resinous and gelatinized material Download PDFInfo
- Publication number
- US1558880A US1558880A US344178A US34417819A US1558880A US 1558880 A US1558880 A US 1558880A US 344178 A US344178 A US 344178A US 34417819 A US34417819 A US 34417819A US 1558880 A US1558880 A US 1558880A
- Authority
- US
- United States
- Prior art keywords
- acids
- gelatinized
- resinous
- oil
- free fatty
- 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
- 239000000463 material Substances 0.000 title description 9
- 239000002904 solvent Substances 0.000 title description 4
- 235000021588 free fatty acids Nutrition 0.000 description 17
- 239000000203 mixture Substances 0.000 description 17
- 239000002253 acid Substances 0.000 description 15
- 239000003921 oil Substances 0.000 description 15
- 235000019198 oils Nutrition 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- 229920005989 resin Polymers 0.000 description 15
- 150000007513 acids Chemical class 0.000 description 12
- 235000015112 vegetable and seed oil Nutrition 0.000 description 12
- 239000008158 vegetable oil Substances 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 150000004665 fatty acids Chemical class 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000004359 castor oil Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000003981 vehicle Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229960001777 castor oil Drugs 0.000 description 5
- 235000019438 castor oil Nutrition 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 5
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000002966 varnish Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- 210000003298 dental enamel Anatomy 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 239000004922 lacquer Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 239000004859 Copal Substances 0.000 description 2
- 241000782205 Guibourtia conjugata Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 230000003292 diminished effect Effects 0.000 description 2
- 239000000025 natural resin Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000350151 Guibourtia demeusei Species 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 244000000231 Sesamum indicum Species 0.000 description 1
- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000004534 enameling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000004426 flaxseed Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- -1 stearic Chemical group 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
Definitions
- This invention relates to vehicles for resinous and similar substances used in varnishes, enamels, impregnating compounds, japans, lacquers, and the like.
- Natural resins such as used for bases of the so-called varnish gums and spirit lacquers, vary greatly in their solubility. Some are soluble incommon solventssuch as alcobenzol, carbon-bisulphide, turpentine, products and others can be only by special solsome prelimihol, petroleum brought into soiution vents or mixtures unless given nary treatment, such as fusion. Drying oils also have been used to some extent as vehicles for such natural resins. If the varnish gums which .are employed are those which requirea preliminary treatment, the fusion operation necessary to render them soluble involves a considerable loss of-material. This is of course undesirable.
- An object of the invention is to produce a vehicle in which these resinous or gelatinized materials may be. incorporated, i. e., resins,
- semi-drying oils such as corn, cotton seed, sesame, rapeseed, and castor oils
- a polyacid alcohol, glycerine on the one hand and, on the other, alkali salts from which can be re cipitated two or more freefatty acids.
- he following fatty acids have been found as being derived in this manner from the oils above mentioned; oleic, stearic, palmitic, myristic, linolenic, isolinolenic, elaeomar- (glaric; arachidic, eru'cic, rapic,'ricinoleio, and ihydroxystearic.
- the free fatty acids may be derived from the vegetable oils by saponifying the oils with an excess ofa solution of caustic soda or otash in water, and after complete saponi cation, decomposin the re-- sulting soaps with a dilute acid, suc as by drochloric acid or sulphuric acid, washing and filtering.
- the mass is kept boiling until complete f clear solution has been obtained.
- Thefatty acids are set free by adding a dilute solution of sulphuric acid (10%) with brisk stirring to the soap solution until the watery under lying layer, which contains the glycerine, shows a distinct' acid reaction to litmus paand fatty acids, which have been set per free, form a uniform clear layer on to of 1 the water.
- the water .is drawn 05 an the fatty acids washed free from mineral acids and salts by repeated treatment with hos water, after which they are filtered dried.
- a homogeneous body is obtained from a vegetable oil by the above process, and adding to it'either a resin, the gelatinn ized product formed by the heating of a vegetable oil at atmosp eric or diminished pressure, the gelatinized product formed by the'combination of a resin'with a vegetable oil, or the gelatinized product formed by the action of glycerine on a resin, it has been found that a homogeneous body is readily obtained.
- the homogeneous body obtained will be a liquid, while in the cases of resins or their gelatinized products, the character of this compound will depend upon the proportion of the acids employed, and the nature of the solid resinous or gelatinized material used.
- a basic material for this composition is formed, preferably, from Congo copal and Chinese wood oil.
- Congo copal and Chinese wood oil By saponification of v the Chinese wood oil and subsequent separation from the glycerine and precipitation of their alkali salts by process described above, a mixture of fatty acids consisting largely of oleic and elaeomargaric acids is obtained.
- Three parts of the Congo co-pal are added to .two parts of this mixture of free fatty acids and heat is applied until a temperature of from 250 to 300 degrees centigrade is reached. After maintainin the mlxture at this temperature for two hours, it is al-- lowed to cool.
- the result is a wax-like product which may readily be used as a asic material in making compounds for the enameling of wire.
- the free fatty acid may be added thereto; and the whole heated to a homogeneous state, thereby yielding a satisfactory material for liquid coating com positions.
- the product formed by the heating of a. vegetable oil with a resin may be dissolved readily in either one or more of the freefatty acids, giving a uniform, syrupy com osition,
- fatty-acids is considered to include any and all classes embraced by the following outline:
- composition of matter which comprises adding free fatty acid to gelatinizedcastor oil.
- composition of matter which comprises gelatinizing vegetable oil and resin, and adding free fatty acid thereto.
- composition of matter comprising gelatinized castor oil and free fatty acid.
- composition of matter comprising free fatty acid, and gelatinized castor oil and co al.
- T e process of forming a composition of matter which comprises adding free fatty acid to gelatinized castor oil, and heating these ingredients to form a homogeneous mass.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Description
Patented Oct. 27, 1925. i
' I UNITED STATES PATENT orrics.
cant.
n. ROCKER, or EAST ORANGE, NEW JERSEY, ASSIGNOR 'ro wnszrnannano rmc I COMPANY, INCORPORATED, OF NEW YORK, N. Y., A CORPORATION OF NEW KOBE.
SOLVENT D MOLE-FOR BESINOUS AND GELATINIZED MATERIAL.
Io Drawing.
To all whom z'tmay con ern.-
Be it known that I, CARL D. HooKER, a
citizen of the United States, residing at East the/county of Essex, State of Orange, in
have invented certain new and New Jersey, useful Improvements hicles for Resinous and Gelatinized Material, of which the following is a full, clear, concise, and exact description.
This invention relates to vehicles for resinous and similar substances used in varnishes, enamels, impregnating compounds, japans, lacquers, and the like.
Natural resins such as used for bases of the so-called varnish gums and spirit lacquers, vary greatly in their solubility. Some are soluble incommon solventssuch as alcobenzol, carbon-bisulphide, turpentine, products and others can be only by special solsome prelimihol, petroleum brought into soiution vents or mixtures unless given nary treatment, such as fusion. Drying oils also have been used to some extent as vehicles for such natural resins. If the varnish gums which .are employed are those which requirea preliminary treatment, the fusion operation necessary to render them soluble involves a considerable loss of-material. This is of course undesirable.
Take for example the usual method employed in treating gums for use in making varnishes. The resin must be subjected to a preliminary fusion until all the residue canbe completely incorporated with the oily vehicle or solvent. A considerable amount 0 the raw material, depending upon the hard-' ness of the resin, isthus lost. If the resin be treated with drying or semidrying oils, only "alimited amount of the resin may be dissolved, the resulting mixture being comparatively low in resin content.
It is well knownthat if vegetable oils are ."subjected to a heat treatment under. the
mosplheric or diminis ressure, 1. e.', either ated pressure depending e nature of the oil, a gelatinous predon t not may be obtained. In case of those proper conditions of vegetable oils which will gelatinize on heat-' ing, the oil will only dissolve about an equal weight of the gel, and for this reason the resu ting solutions have been relatively d1- lute. M
,An object of the invention is to produce a vehicle in which these resinous or gelatinized materials may be. incorporated, i. e., resins,
Application filed December 11, 1919. Serial No. 344,178.
7 the gelatinized products of overheating of an oil and By completely saponi'fying drying oils such as linseed and Chinese wood oils, or
in Solvents and -Ve-.
.has been used to accomplish t v vegetable oils and the gelatinous masses formed by the resin.
semi-drying oils such a as corn, cotton seed, sesame, rapeseed, and castor oils, there is produced a polyacid alcohol, glycerine, on the one hand and, on the other, alkali salts from which can be re cipitated two or more freefatty acids. he following fatty acids have been found as being derived in this manner from the oils above mentioned; oleic, stearic, palmitic, myristic, linolenic, isolinolenic, elaeomar- (glaric; arachidic, eru'cic, rapic,'ricinoleio, and ihydroxystearic. The free fatty acids may be derived from the vegetable oils by saponifying the oils with an excess ofa solution of caustic soda or otash in water, and after complete saponi cation, decomposin the re-- sulting soaps with a dilute acid, suc as by drochloric acid or sulphuric acid, washing and filtering. One laboratory rocess which is is the following: One kilo of the oil is heated to about 80 C. and a solution of 50 ms caustic soda in 600 c. c. of water is ad ed with con stant stirring. The emulsion formed is heat= ed to boiling, and a solution of'150 grams caustic soda in 1200 c. 0. water is-added.
The mass is kept boiling until complete f clear solution has been obtained. Thefatty acids are set free by adding a dilute solution of sulphuric acid (10%) with brisk stirring to the soap solution until the watery under lying layer, which contains the glycerine, shows a distinct' acid reaction to litmus paand fatty acids, which have been set per free, form a uniform clear layer on to of 1 the water. The water .is drawn 05, an the fatty acids washed free from mineral acids and salts by repeated treatment with hos water, after which they are filtered dried. By taking one of the above fatty acids or a mixture of them as. is obtained from a vegetable oil by the above process, and adding to it'either a resin, the gelatinn ized product formed by the heating of a vegetable oil at atmosp eric or diminished pressure, the gelatinized product formed by the'combination of a resin'with a vegetable oil, or the gelatinized product formed by the action of glycerine on a resin, it has been found that a homogeneous body is readily obtained. In thecase of the treatment with the acids of the gelatinized product formed by the heating of the vegetable oil at atmospheric or diminished pressure, the homogeneous body obtained will be a liquid, while in the cases of resins or their gelatinized products, the character of this compound will depend upon the proportion of the acids employed, and the nature of the solid resinous or gelatinized material used.
The adaptation of such compounds as mentioned herein for enamels, impregnating compounds, japans, lacquers, and varnishes has been proven by tests which have been made and the value of the discovery of this property'of the free fatty acids and its application will be apparent to one skilled in the art.
An example of the use of these free fatty acids as vehicles for the above mentioned substances is shown in the preparation of a li uid composition for application to electrical conductors as an insulating enamel or japan. A basic material for this composition is formed, preferably, from Congo copal and Chinese wood oil. By saponification of v the Chinese wood oil and subsequent separation from the glycerine and precipitation of their alkali salts by process described above, a mixture of fatty acids consisting largely of oleic and elaeomargaric acids is obtained. Three parts of the Congo co-pal are added to .two parts of this mixture of free fatty acids and heat is applied until a temperature of from 250 to 300 degrees centigrade is reached. After maintainin the mlxture at this temperature for two hours, it is al-- lowed to cool. The result is a wax-like product which may readily be used as a asic material in making compounds for the enameling of wire.
In the manner described above, after subjecting a vegetable oil, such as Chinese wood oil to heat and obtaining a gelatinized product therefrom, the free fatty acid may be added thereto; and the whole heated to a homogeneous state, thereby yielding a satisfactory material for liquid coating com positions. So also the product formed by the heating of a. vegetable oil with a resin may be dissolved readily in either one or more of the freefatty acids, giving a uniform, syrupy com osition,
' Moreover, as wil be seen from my prior Patent No. 1,422,861, granted July 18, 1922, the free fatty acids afford a means by which resins may be more easily treated with glycerine in order to form the specific coatlng composition covered by that application.
While there has been named herein a s e- ClfiC number of resinous materials whlch may be utilized in preparing liquid coating compositions according to the invention, it is intended to include all substances of resinous or gelatinized-oleaginous nature, which are adapted for such use when one or more of the free fatty acids are used as the vehicle.
In order that it may be understood what acids are intended to be included as belonging to the fatty acid class, a word of explanation is considered to be necessary. Vari ous textbooks which contain matter relating to the chemical" composition of such substances difi'er in their classification of the fatty acids. As used in this specification, the term fatty-acids is considered to include any and all classes embraced by the following outline:
l. Acids of the acetic series, C H nO 2. Acids of the oleic series, C H O 3. Acids of the series C H O which includes the open chain and cyclic series.
4. Acids of the linoleic series, C H O 5. Acids of the clupanodonic and the C H O series.
6. Hydroxylated or carboxylated acids of any of the above series.
What is claimed is:
1. The process of forming a composition of matter which comprises adding free fatty acid to gelatinizedcastor oil.
2. The process of forming a composition of matter which comprises gelatinizing vegetable oil and resin, and adding free fatty acid thereto.
3. The process of forming a -composition of matter which comprises gelatinizing castor oil and copal, and adding free fatty acid thereto.
4. A composition of matter comprising gelatinized castor oil and free fatty acid.
5. A composition of matter comprising free fatty acid, and gelatinized castor oil and co al.
6. T e process of forming a composition of matter which comprises adding free fatty acid to gelatinized castor oil, and heating these ingredients to form a homogeneous mass.
7. The process of forming a composition of matter which comprises gelatinizing vegetable oil and resin, adding free fatty acid thereto and heating the resulting product to a homogeneous state.
8. The process of forming a composition of matter which comprises gelatinizing cas tor oil and copal, adding free fatty acid thereto and heating the resulting product to a homogeneous state.
In witness whereof, I hereunto subscribe my name this 10th day of December A. D.,
CARL D. HOCKER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US344178A US1558880A (en) | 1919-12-11 | 1919-12-11 | Solvent and vehicle for resinous and gelatinized material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US344178A US1558880A (en) | 1919-12-11 | 1919-12-11 | Solvent and vehicle for resinous and gelatinized material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1558880A true US1558880A (en) | 1925-10-27 |
Family
ID=23349383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US344178A Expired - Lifetime US1558880A (en) | 1919-12-11 | 1919-12-11 | Solvent and vehicle for resinous and gelatinized material |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1558880A (en) |
-
1919
- 1919-12-11 US US344178A patent/US1558880A/en not_active Expired - Lifetime
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