US2165857A - Solidified normally liquid substances - Google Patents
Solidified normally liquid substances Download PDFInfo
- Publication number
- US2165857A US2165857A US172922A US17292237A US2165857A US 2165857 A US2165857 A US 2165857A US 172922 A US172922 A US 172922A US 17292237 A US17292237 A US 17292237A US 2165857 A US2165857 A US 2165857A
- Authority
- US
- United States
- Prior art keywords
- glycerine
- normally liquid
- liquid substances
- products
- solidified
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L7/00—Fuels produced by solidifying fluid fuels
- C10L7/02—Fuels produced by solidifying fluid fuels liquid fuels
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/06—Solidifying liquids
Definitions
- This invention relates to a process for solidifying normally liquid substances, such as liquid polyhydric alcohols, and to the solidified products obtained thereby.
- saturated fatty alzo cchols of the group C6--Ci8, for example myristyl-, palmityl-, docosyland myricyl alcohol, or technical mixtures of same, are adapted to solidify glycerine and glycol respectively.
- This action may exactly be controlled by th 5 joint use of chemical compounds of sapona'ceous character, such as salts of the sulphuric acid esters of fatty alcohols, or of fatty-acid condensation products, or the like. Depending on the relative proportions of the substances employed, so the resulting products are similar to Vaseline, or also opaque salves and lubricants. Nearly solid preparations can also be obtained with the agents specified.
- emulgents i. e. emulsifying and dispersingly acting substances, which do not have an alkaline reaction in anaqueous" solution.
- Such- 40 substances are first of all the neutralization products of sulphuric acid esters (a) Of fatty alcohols, i. e. of higher molecular aliphatic alcohols with at least 8 carbon atoms and (b) 0f monoand di-glycerides respectively of higher molecular fatty acids.
- sulphuric acid esters (a) Of fatty alcohols, i. e. of higher molecular aliphatic alcohols with at least 8 carbon atoms and (b) 0f monoand di-glycerides respectively of higher molecular fatty acids.
- water soluble organic products for instance, the sulphuric acid esters of low molecular oxyalkylamines, as aminoethyl-sulphuric acid, or the onand aminoaikyl-acid sulphides respectively, for example, oxyethanacid sulphide or aminoethan- 5 acid sulphide, or the decomposition products of albumen as for instance lysalbic acid.
- the sulphuric acid esters of low molecular oxyalkylamines as aminoethyl-sulphuric acid, or the onand aminoaikyl-acid sulphides respectively, for example, oxyethanacid sulphide or aminoethan- 5 acid sulphide, or the decomposition products of albumen as for instance lysalbic acid.
- Gelatinous preparations applicable with vantage as lubricants and anti-friction agents for technical p poses, can be produced in extensive l0 variety.
- the present process enables the products to be adapted to meet the chief physical properties required for their technical application, such as the consistency which is retained even at low temperatures, by judicious selection of erent ingredients and their proportions in the ture.
- the resulting products both as such, and also after the addition of fillers such as starch, agar-agar, dimethylcellulose, and the like, or substances with a medicinal or cosmetic action, form valuable preparations for the care of the skin or for pharmaceutical purposes.
- glycerine substitutes such as slycols (ethylene-, butyleneand pentamethylene glycols) aqueous sugar solutions, and the like, may also be solidified by the present process.
- Glycerine and glycols can be used both in the anhydrous form and diluted with water.
- the products obtained by the process o! the invention may be arranged to have an acid, neutral, or alkaline reaction. The following examples will serve to illustrate the invention.
- Example I 9 parts by weight of myristyl alcohol are melted down, with 90 parts by weight of anhydrous glycerine, on the water bath, and 1 part by weight of sodium cetyl-sulphate and 10 parts by weight of starch are stirred in. The stirring of the mass is continued until cold, 9. semi-solid, unctuous 55 the skin, being obtained.
- Example III 8 parts by weight of a technical mixture. consisting of approximately equal parts of palmityland stearylalcohol, are melted down on the water bath with 2 parts by' weight of triethanolamine .dodecylphosphate and 80 parts by weight of hydrated (80%) glycerine, and treated with 2 parts by weight of salicylic acid, the whole being stirred until cold.
- An excellent agent for the pediculture 2,185,857 mass, forming a good medium for the care 01 a sulphuric acid ester oi a fatty alcohol having at least 8 carbon atoms in admixture with myristyl alcohol, said mixture being in an amount suflicient to solidify said substance.
- a solid composition of matter comprising a substance selected from the group consisting oi. glycerine, glycols, and aqueous sugar solutions, in combination with sodium cetbl sulphate in admixture with myristyl alcohol, said'mixture being in an amount suflicient to solidify said substance.
- a solid composition 01' matter comprising a substance selected from the group consisting of glycerine, glycols, and aqueous sugar solutions, in combination with about 840% myristyi alcohol and 1-2% of a neutralization product of a sulphuric acid ester of a fatty alcohol having at least 8 carbon atoms.
Description
This invention relates to a process for solidifying normally liquid substances, such as liquid polyhydric alcohols, and to the solidified products obtained thereby.
It has been proposed to solidify glycerine by an addition of sodium stearate, or soap made from hard fats, in association, if desired, with other agents. Glycerine thus solidified may also be worked up into lubricants, anti-friction agents,
salves, or the like. Naturally, owing to their content of soap, such products have an alkaline reaction which, as is well mown, is undesirable in many instances. Moreover, the purpose for which they are to be used precludes the additional use of agents with an acid reaction, such as salicylic acid or the like. Again, the addition of substances, such as zinc oxide, which react with soap, is usually impossible.
It has now been found that saturated fatty alzo cchols of the group C6--Ci8, for example myristyl-, palmityl-, docosyland myricyl alcohol, or technical mixtures of same, are adapted to solidify glycerine and glycol respectively.
This action may exactly be controlled by th 5 joint use of chemical compounds of sapona'ceous character, such as salts of the sulphuric acid esters of fatty alcohols, or of fatty-acid condensation products, or the like. Depending on the relative proportions of the substances employed, so the resulting products are similar to Vaseline, or also opaque salves and lubricants. Nearly solid preparations can also be obtained with the agents specified.
In order to distribute these alcohols in .the
35 most suitable manner in the glycerine and glycol respectively, the joint use of mown emulgents, i. e. emulsifying and dispersingly acting substances, which do not have an alkaline reaction in anaqueous" solution, is recommended. Such- 40 substances are first of all the neutralization products of sulphuric acid esters (a) Of fatty alcohols, i. e. of higher molecular aliphatic alcohols with at least 8 carbon atoms and (b) 0f monoand di-glycerides respectively of higher molecular fatty acids. v s
For many purposes the neutralization products of sulphurated unsaturated mineral oils, sulphurated castor oils, sulphurated fatty acids of 50 castcr oils, sulphurated fatty acids of fish oil also may be used. Finally those fatty acid condensation produc represent excellent emulgents which are obtained by condensing higher molecular fatty acids in 55 the form of their haloids with the most various wing. Application rial No. 172,922.
lctb,
.. Snack, iiu, Ger- Novemher 5, 137, So-
a Novemr 1'7,
water soluble organic products, for instance, the sulphuric acid esters of low molecular oxyalkylamines, as aminoethyl-sulphuric acid, or the onand aminoaikyl-acid sulphides respectively, for example, oxyethanacid sulphide or aminoethan- 5 acid sulphide, or the decomposition products of albumen as for instance lysalbic acid.
Gelatinous preparations, applicable with vantage as lubricants and anti-friction agents for technical p poses, can be produced in extensive l0 variety.
The joint employment of skin emollients, such as salicylic acid or the like, and also of antic'orrosive agents in the case of preparations used as lubricants for special purposes in the W 1 chinery industry, is also easily possible.
The present process enables the products to be adapted to meet the chief physical properties required for their technical application, such as the consistency which is retained even at low temperatures, by judicious selection of erent ingredients and their proportions in the ture. Finally, the resulting products, both as such, and also after the addition of fillers such as starch, agar-agar, dimethylcellulose, and the like, or substances with a medicinal or cosmetic action, form valuable preparations for the care of the skin or for pharmaceutical purposes.
In addition to glycerine, the so-called glycerine substitutes, such as slycols (ethylene-, butyleneand pentamethylene glycols) aqueous sugar solutions, and the like, may also be solidified by the present process. Glycerine and glycols can be used both in the anhydrous form and diluted with water. The products obtained by the process o! the invention may be arranged to have an acid, neutral, or alkaline reaction. The following examples will serve to illustrate the invention.
' Example I Example I! 9 parts by weight of myristyl alcohol are melted down, with 90 parts by weight of anhydrous glycerine, on the water bath, and 1 part by weight of sodium cetyl-sulphate and 10 parts by weight of starch are stirred in. The stirring of the mass is continued until cold, 9. semi-solid, unctuous 55 the skin, being obtained.
Example III 8 parts by weight of a technical mixture. consisting of approximately equal parts of palmityland stearylalcohol, are melted down on the water bath with 2 parts by' weight of triethanolamine .dodecylphosphate and 80 parts by weight of hydrated (80%) glycerine, and treated with 2 parts by weight of salicylic acid, the whole being stirred until cold. An excellent agent for the pediculture 2,185,857 mass, forming a good medium for the care 01 a sulphuric acid ester oi a fatty alcohol having at least 8 carbon atoms in admixture with myristyl alcohol, said mixture being in an amount suflicient to solidify said substance.
2. A solid composition of matter comprising a substance selected from the group consisting oi. glycerine, glycols, and aqueous sugar solutions, in combination with sodium cetbl sulphate in admixture with myristyl alcohol, said'mixture being in an amount suflicient to solidify said substance.
3. A solid composition 01' matter comprising a substance selected from the group consisting of glycerine, glycols, and aqueous sugar solutions, in combination with about 840% myristyi alcohol and 1-2% of a neutralization product of a sulphuric acid ester of a fatty alcohol having at least 8 carbon atoms.
' SIMON JACOBOWI'IZ.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2165857X | 1936-11-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2165857A true US2165857A (en) | 1939-07-11 |
Family
ID=7988157
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US172922A Expired - Lifetime US2165857A (en) | 1936-11-17 | 1937-11-05 | Solidified normally liquid substances |
Country Status (1)
Country | Link |
---|---|
US (1) | US2165857A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2643229A (en) * | 1953-06-23 | Nonsoap synthetic detergent in | ||
US2651829A (en) * | 1949-01-12 | 1953-09-15 | Metallgesellschaft Ag | Surface active media |
US2990371A (en) * | 1959-07-23 | 1961-06-27 | Ellenson Evelyn | Lubricant composition |
US3888995A (en) * | 1968-07-19 | 1975-06-10 | Syntex Corp | Fatty alcohol-propylene glycol vehicle |
US6416749B1 (en) * | 1992-10-15 | 2002-07-09 | Schering-Plough Healthcare Products, Inc. | Treatment for onychomycosis topically applying salicylic acid, optionally in combination with a retinoid |
-
1937
- 1937-11-05 US US172922A patent/US2165857A/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2643229A (en) * | 1953-06-23 | Nonsoap synthetic detergent in | ||
US2651829A (en) * | 1949-01-12 | 1953-09-15 | Metallgesellschaft Ag | Surface active media |
US2990371A (en) * | 1959-07-23 | 1961-06-27 | Ellenson Evelyn | Lubricant composition |
US3888995A (en) * | 1968-07-19 | 1975-06-10 | Syntex Corp | Fatty alcohol-propylene glycol vehicle |
US6416749B1 (en) * | 1992-10-15 | 2002-07-09 | Schering-Plough Healthcare Products, Inc. | Treatment for onychomycosis topically applying salicylic acid, optionally in combination with a retinoid |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3033755A (en) | Process for removing the water soluble materials from a keratin structure and cosmetic or pharmaceutical product formed therefrom | |
US3542919A (en) | Astringent alkali metal aluminum complexes of hydroxy acids | |
US4370319A (en) | Skin conditioning compositions | |
US3846556A (en) | Water-in-oil emulsions, cosmetic products made therefrom and method of making said cosmetic products | |
EP0216557A2 (en) | Translucent water-in-oil emulsions | |
CA1138342A (en) | Cholesterol emulsifier in cosmetics | |
US2241331A (en) | Suppository | |
US2820768A (en) | Soaps and their methods of preparation | |
US3259545A (en) | Stable aluminum hydroxide gel or aluminum hydroxide-sodium zirconium lactate antiperspirant stick | |
US4035514A (en) | Water washable petrolatum compositions | |
US2165857A (en) | Solidified normally liquid substances | |
US5362418A (en) | Gel-like emulsion and O/W emulsion obtained from the gel-like emulsion | |
US5294435A (en) | Stabilization of emulsion additives to nail polish removers | |
EP0062352B1 (en) | Soap composition | |
US2294229A (en) | Cosmetic preparations | |
US2086479A (en) | Stable emulsion and method of producing the same | |
EP0273619B1 (en) | Cosmetic composition | |
US1999161A (en) | Skin cream containing magnesium | |
US3624208A (en) | Floating bath oil composition | |
US2361756A (en) | Ointments and the like | |
US2164717A (en) | Brushless shaving cream | |
US2532206A (en) | Ointment base of glycerine with phosphatide and petrolatum | |
US2121305A (en) | Manufacture of emulsions | |
US2079166A (en) | Topical preparation | |
AT156593B (en) | Process for the solidification of glycerine or glycerine substitutes. |