USRE20361E - Frocess of producing emulsions - Google Patents

Frocess of producing emulsions Download PDF

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USRE20361E
USRE20361E US20361DE USRE20361E US RE20361 E USRE20361 E US RE20361E US 20361D E US20361D E US 20361DE US RE20361 E USRE20361 E US RE20361E
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fatty acids
emulsions
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/017Mixtures of compounds
    • C09K23/018Mixtures of two or more different organic oxygen-containing compounds

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  • This invention relates to a process of producing emulsions in which partially esterified polyhydric alcohols or derivatives thereof are employed in conjunction with fatty acids of high molecular weight or derivatives thereof, as emulsifying agents. It has been found that these partially esterifled compounds, in so far as they still contain free alcoholic hydroxyl groups, possess the property of forming very stable emulsions with water or aqueous solutions in the presence of substances with an alkaline reaction, such emulsions remaining stable even at elevated temperatures.
  • estersof this kind are for example the monoor di-glycerol esters and the monoor di-glycol esters, such as glycol mono-oleic acid ester (glycol mono-oleate).
  • esters of the polyhydric alcohols are however also eminently adaptable for this purpose, provided these esters possess non-esterified alcoholic hydroxyl groups.
  • the esters of the hydroxylated fatty acids have been found to be advantageous and relatively easily obtainable, as well as esters which contain ethereal poly-compounds of' polyhydric alcohols as alcoholic components.
  • the ethereal poly-compounds may have similar and dissimilar alcohol radicles, and the hydroxy compounds of fatty acids, the singly and poly-unsaturated 'monobasic aliphatic acids come into consideration as derivatives of fatty acids with high molecular weight. Examples of these are the di-glyceride of the a-hydroxy'stearic acid, the mono glycol ester of oleic acid and triethylene glycol mono stearate.
  • these substances are emulsified either alone or in conjunction with other substances, with water or aqueous solutions in the presence of substances with an alkaline reaction.
  • the added substances can be of very diverse natures, for example fats, fatty acids,- waxes, resins, vegetable or mineral oils of all kinds, colloids such as rubber, glue, gelatine, dextrine and also terpenes, perfumes, animal and plant emulsions (latex, cow's milk) lamp-black, talc, zinc oxide and thelike can be employed.
  • a particularly excellent effect has been produced by adding the above described esters to aqueous emulsions of wool-grease.
  • aqueous wool-grease emulsions can be produced by intimately admixing wool-grease and water by rubbing, kneading or the like. These emulsions form relatively viscid salves or ointments, even when they contain as much as per cent of water. greasy layer is formed which is not easily ab- On rubbing the same on the skin, a
  • perfumes and the like can be added to the emul- :5,
  • the emulsions are preferably produced by melting down the ester-soluble substances such as fats, waxes,
  • the water or the aqueous solution to be employed which also contains the substances having analkaline reaction.
  • esters suitable for emulsification naturally neednot be effected by employing individual acids and alcohols. On the contrary, mixtures of the same can be employed, such as those which occur in the natural state or are available in technical processes.
  • th'ese'starting materials are subjected to a corresponding purification,
  • the acids, obtained in the saponification of oleag'inous matter, such as oils, fats and waxes by steam or alkali are suitable raw materials for the production of esters adapted to act as emulsifying agents, olive oil, ground nut oil, linseed oil, rape-seed oil, coconut fat, wool-grease and Mont'an wax may be mentioned as examples of such oils, fats and waxes.
  • Partially esterified glycols carrying fatty acids of high molecular weight can be prepared by.
  • sired glycol esters, the alkali salts of the corresponding fatty acids, and an emulsion can be obtained immediately on treating the product with water, without it being first necessary to add separately salts with an alkaline reaction.
  • An emulsion of this nature can be prepared for example in the following manner:
  • ammonium stearate (alkaline substance) employed amounts to about 11 per cent by weight of the glycerine di-stea'rate.
  • Emulsions prepared in accordance with the present invention can be employed with advantage in processes of wetting, impregnating and rendering soft and pliable fibrous or artificial materials, paper or similar materials. They can also be employed as lubricating agents, for example as solid lubricants such as Staufi'er greases. They are also of advantage for cosmetic and "pharmaceutical purposes, and likewise for the production of margarine and the like, that is of emulsions adapted to be used in foods, as
  • esters on account of their emulsifying action when employed, in conjunction with substances having an 'alkaline reaction, are well adapted for washing and cleaning purposes,.to I
  • Another field of application of the abovedescribed emulsions is the fatting of fibrous materials, for example, the oiling of wool.
  • fibrous materials for example, the oiling of wool.
  • the efllcacy of the means hitherto employed has been very unsatisfactory in many ways.
  • the fibres were only covered on the exterior with a film of fat and remained to all intents and purposes just as hard and brittle as they were originally.
  • esters hereinbefore referred to have also been found to be excellent for the washing of raw wool for example.
  • the more easily alkali content of which is far less than 1 per cent exhibit such an excellent washing effect that the washed product is obtained in an unusually clean state.
  • esters themselves are pro-eminently suitable for the most diverse purposes. They can be used per se or in combination with the hereinbefore specified substances which can be added to the emulsions.
  • the addition of acid or basic substances as the case may be is of particular advantagein order to weaken or to neutralize basic or acid substances during the operation.
  • a case of this kind arises for example in the treatment of weighed silk fibres with glycerine stearic ester, to which some potash soap has been added.
  • Silk, cotton and wool yarns can be treated with ease with these esters or mixtures or solutions thereof, 'I'hey thereby obtain 'a strength and suppleness which has ne'verpreviously been attamed, so that thread breakage's, which frequently occurred during the weaving process, are almost completely obviated.
  • a further sphere of application of these esters resides in their additionto oil-colors. Inthis case they prevent the pigment settling out when the paint is allowed to stand. For example, if glycol-monostearic ester is added to the customary red lead linseed oil paint, even 1.5 per cent is suillcient to prevent the settling-out of the pigment, without the paint being detrimentally influenced thereby.
  • polyhydric alcohols partially esterifled with any derivatives of fatty acids of high molecular weightand particularly their hydroxyare emulsified with water or aqueous solutions of any substances in the presence of small amounts of substances having an alkaline reaction.
  • a process for the production of emulsions in which ethereal poly-compounds of at least one polyhydric alcohol partially esterified with acids selected'from a group consisting of fatty acids acids, are emulsified with water or aqueous solutions of any substances in the presence of small amounts of substances having an alkaline reaction.
  • emulsions In the production of emulsions, the process which comprises emulsifying in the presence of small amounts of alkaline reacting substances, ethereal poly-compounds of at least one polyhydric alcohol, partially esterified with high molecular fatty acids, with water and with oleaginous matter selected from a class consisting of fats, fatty acids, waxes, vegetable oils and mineral oils.
  • the process which comprises reacting alkyline oxids with fatty acids of high molecular weight in the presence of an aqueous solution of alkali salts of said fatty acids as catalysts, thereby producing a mixture of partially esterified glycol esters and alkali oleaginous'matter selected from a class consisting of fatty acids, naturalfats and fatty acid containing oils in the presence of an aqueoussolution of alkali salts of said fatty acids as catalysts, thereby producing a mixture of partially esterified glycol esters and alkali salts of said fatty acids, and emulsifying the said resulting mixture with water or aqueous solutions of suitable substances.
  • an emulsion comprising water, polyhydric alcohols partially esterified with acids selected from a class consisting of derivatives of fatty acids of high molecular weight, .hydroxy-compounds of said fatty acids and unsaturated derivatives of said fatty acids; and'also containing small amounts of substances of alkaline reaction.
  • an emulsion comprising water, polyhydric alcohols, partially esterified with acids selected from a class consisting of derivatives of fatty acids of high molecular weight, hydroxy-compounds of said fatty acids and unsaturated derivatives of .said fatty acids;
  • oleaginous matter selected from a class consisting of fatty acids, waxes, natural fats and oils; and also containing small amounts of substances of alkaline reaction.
  • Theprocess of forming an emulsion of oilwith water which comprises incorporating therewith an emulsifying agentconsisting essentially of ethereal poly-compounds of at least one polyhydric alcohol partially esterified with acids se-' lected from a group consisting of derivatives of fatty acids of high molecular weight, hydroxycompounds of said fatty acids and umaturated derivatives of said fatty acids and a quantity of soap suilicient to increase materially the stability of the emulsion, but not substantially in excess 5 ,of ten per cent based onthe weight of the p ym 13.
  • the process which comprises emulsifying oleaginous matter selected from a classcomistingoffats. l0 fatty acids, waxes, vegetable oils and mineral oils,
  • an emul- 20 sion comprising oil, water; polyhydric alcohols partially esterlfled with acidsgelected from a class fatty acids and unsaturated derivatives of said' fatty acids; and also containing soap in amount sumcient to m, materially the stabflity of the emulsion, but not substantially in excess of ten per cent bas'ed'on the weight of the partially 15.
  • an emulsion comprising water, polyhydric alcohols par tiaily esterli'ied with acids selected from a class consisting of derivatives of fatty acids and unsaturated derivatives of said fatty acids; oleaginous matter selected ,from a class consisting of fatty acids, waxes, natural fats and oils; and also containing soap in amount suilicient to increase materially the stability of the emulsion. but not substantially in excess of ten'per cent based on the w isht oi the partially esterifled polyhydric alcohols.

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Description

Reissued May 11, 1937' umreo STATES faceless 0F rnonuomo infusions Hans Schrader, Essen-Ruhr, Germany, assignor' to the firm Th. Goldschi'nidt A.-G., Essen-Ruhr,
No Drawing. Original 1%. 1,826,900, dated 0cm 1 ber 13, 1931, Serial No. 314,837, October 24,
1928, Application for reissue October 7, 1933,
Serial No. 692,697.
15 Claims.
This invention relates to a process of producing emulsions in which partially esterified polyhydric alcohols or derivatives thereof are employed in conjunction with fatty acids of high molecular weight or derivatives thereof, as emulsifying agents. It has been found that these partially esterifled compounds, in so far as they still contain free alcoholic hydroxyl groups, possess the property of forming very stable emulsions with water or aqueous solutions in the presence of substances with an alkaline reaction, such emulsions remaining stable even at elevated temperatures. Among estersof this kind are for example the monoor di-glycerol esters and the monoor di-glycol esters, such as glycol mono-oleic acid ester (glycol mono-oleate). The derivatives of esters of the polyhydric alcohols are however also eminently adaptable for this purpose, provided these esters possess non-esterified alcoholic hydroxyl groups. In particular the esters of the hydroxylated fatty acids have been found to be advantageous and relatively easily obtainable, as well as esters which contain ethereal poly-compounds of' polyhydric alcohols as alcoholic components. The ethereal poly-compounds may have similar and dissimilar alcohol radicles, and the hydroxy compounds of fatty acids, the singly and poly-unsaturated 'monobasic aliphatic acids come into consideration as derivatives of fatty acids with high molecular weight. Examples of these are the di-glyceride of the a-hydroxy'stearic acid, the mono glycol ester of oleic acid and triethylene glycol mono stearate.
In order to prepare the emulsions these substances are emulsified either alone or in conjunction with other substances, with water or aqueous solutions in the presence of substances with an alkaline reaction. The added substances can be of very diverse natures, for example fats, fatty acids,- waxes, resins, vegetable or mineral oils of all kinds, colloids such as rubber, glue, gelatine, dextrine and also terpenes, perfumes, animal and plant emulsions (latex, cow's milk) lamp-black, talc, zinc oxide and thelike can be employed.
A particularly excellent effect has been produced by adding the above described esters to aqueous emulsions of wool-grease. As is known I aqueous wool-grease emulsions can be produced by intimately admixing wool-grease and water by rubbing, kneading or the like. These emulsions form relatively viscid salves or ointments, even when they contain as much as per cent of water. greasy layer is formed which is not easily ab- On rubbing the same on the skin, a
In Germany August 2'1, 1927 sorbed by the skin. The reason for this property is the structure of the emulsion, in which the water is distributed in small droplets throughout the wool-grease and in which the wool grease consequently constitutes the external continuous phase. Hence the relatively poor rubbing power and greasy property of these ordinary emulsions being continuous. These emulsions possess much more favorable properties, in particular they have i a very ready spreading power, and the fat is absorbed by the skin with surprising rapidity on account of its fine state of subdivision. The proportions in mixtures of wool-grease, ester and water can be varied within wide limits; moreover a whole series of substances as for example glycerine, petroleum jelly, spermaceti, talc, borax,
perfumes and the like, can be added to the emul- :5,
sions.
In carrying out the present invention, the emulsions are preferably produced by melting down the ester-soluble substances such as fats, waxes,
oils and the like in the esters and then gradually stirring into the melt produced, the water or the aqueous solution to be employed, which also contains the substances having analkaline reaction.
The production of the esters suitable for emulsification naturally neednot be effected by employing individual acids and alcohols. On the contrary, mixtures of the same can be employed, such as those which occur in the natural state or are available in technical processes. vAccording to the purpose of employment and the requirements with respect to purity of color and odor and the like, of the finished product, th'ese'starting materials are subjected to a corresponding purification, Thus, for example/the acids, obtained in the saponification of oleag'inous matter, such as oils, fats and waxes by steam or alkali, are suitable raw materials for the production of esters adapted to act as emulsifying agents, olive oil, ground nut oil, linseed oil, rape-seed oil, coconut fat, wool-grease and Mont'an wax may be mentioned as examples of such oils, fats and waxes. Moreover, esters obtained by the re-esterification of such acids with polyhydric alcohols, such as glycol or glycerol can be used for, the aforesaid purpose.
. Partially esterified glycols carrying fatty acids of high molecular weight can be prepared by.
sired glycol esters, the alkali salts of the corresponding fatty acids, and an emulsion can be obtained immediately on treating the product with water, without it being first necessary to add separately salts with an alkaline reaction.
An emulsion of this nature can be prepared for example in the following manner:
5 kgs. of stearic acid are heated with 1kg. ethylene oxide, after the addition of 5 gr. NaOH, in an autoclave for several hours. The product obtained in this manner is emulsified with 18 kgs. of a 25 per cent glycerine solution at a temperature of 60"-'l0 C. On cooling 9. fine soft, white salve or ointment is produced which no longer gives a basic reaction with red litmus paper. In this example the NaOH (alkaline substance) employed amounts to about 0.5 per cent by weight of the glycol stearate formed by the reaction.
The following are further examples of the production'of emulsions:
In making an emulsion containing 45 per cent lubricating oil, 4.5 per cent of glycerine di-stea-' rate, 0.5 per cent ammonium stearate and 50 per cent water, the ester is dissolved in they lubricating oil which is heated up to about 75 0., where* upon the water is added with continual stirring.- A creamy, smooth emulsion is obtained, which is applicable as a greasing and lubricating agent for the most diverse purposes.
In this example the ammonium stearate (alkaline substance) employed amounts to about 11 per cent by weight of the glycerine di-stea'rate.
In making another emulsion containing 20 per cent petroleum jelly, 19 per cent of tri-ethylene glycol monc-stearate, 1 per cent potassium stearate and 60 per cent water, the petroleum jelly, ester and potassium stearate are melted down together at about 70 C. The water is gradually added to the melted mass with continual stirring.- A fine uniform stable emulsion is produced in which the aqueous liquid forms the outer continuous phase. In this example the potassium stearate (alkaline substance) employed amounts to about per cent by weight of the tri-ethylene glycol mono-stearate. From the above specific examples it is seen that small amounts, ranging from about 0.5 to 11 per cent, of substances having an alkaline reaction are required in my process of producing emulsions, these quantities being based on the weight of partially esterifled polyhydric alcohols present. Emulsions prepared in accordance with the present invention can be employed with advantage in processes of wetting, impregnating and rendering soft and pliable fibrous or artificial materials, paper or similar materials. They can also be employed as lubricating agents, for example as solid lubricants such as Staufi'er greases. They are also of advantage for cosmetic and "pharmaceutical purposes, and likewise for the production of margarine and the like, that is of emulsions adapted to be used in foods, as
well as for the production of boot polishes and polishing waxes.
The esters on account of their emulsifying action when employed, in conjunction with substances having an 'alkaline reaction, are well adapted for washing and cleaning purposes,.to I
of the above-described esters.
which end, special ingredients, such as boric acid, oil of turpentine, tetra-hydro naphthalene and the like can be added. They can also be employed advantageously as superfatting agents for soaps. In particular a special technical washing effect can be produced by employing the esters in conjunction with soaps or substances having a similar action, such as saponin or the like. Thus the.
addition of 5 per cent of ethylene glycol-monostearate to ordinary soap results in a product which dlfiers very advantageously from the initial soap. The foam produced is of a particular creamy nature and good consistency and the washing action of thesoap is considerably enhanced by the addition. Moreover the product possesses the property, in its use in toilet soaps, of imparting a pleasant suppleness to the skin after washing, similar to that produced by the ointments made from the esters. A further advantage is the pure white color of the ester, whereas most other superfatting agents are more or less strongly colored.
Another field of application of the abovedescribed emulsions is the fatting of fibrous materials, for example, the oiling of wool. As is well known it is necessary to impregnate the washed wool to be spun with emulsions of fats or oils with soaps 'or alkalies, in order that the wool may posses the requisite smoothness and suppleness during the spinning process. The efllcacy of the means hitherto employed however has been very unsatisfactory in many ways. The fibres were only covered on the exterior with a film of fat and remained to all intents and purposes just as hard and brittle as they were originally. Moreover it was diflicult to remove the fat-layer from the individual wool-fibres after finishing the spunyarn. Even if the washing previous to dyeing was carried out as carefully as possible, the yarns which had been tightly spun crinkled and were useless for further treatment. All these disadvantages are obviated if wool oiling agents are employed which contain even small percentages with the use of these .esters milk like emulsions are obtained which possess an outstanding wetting-power. The stability of the emulsified phase is so great, that the addition of adhesive agents is not necessary. After spinning the oils are removed completely, even from hard twisted threads, by simple rinsing in tepid, very weakly alkaline baths, this havlng'an absolutely non-injurious eifect.
The esters hereinbefore referred to have also been found to be excellent for the washing of raw wool for example. When these esters are added to the wool washing baths, then the more easily alkali content of which is far less than 1 per cent, exhibit such an excellent washing effect that the washed product is obtained in an unusually clean state.
It has already been stated that not only the emulsions derived from the aforesaid esters, but also the esters themselves are pro-eminently suitable for the most diverse purposes. They can be used per se or in combination with the hereinbefore specified substances which can be added to the emulsions. In this connection it should compounds or theirv unsaturated dcrivativesbe pointed out that the addition of acid or basic substances as the case may be, is of particular advantagein order to weaken or to neutralize basic or acid substances during the operation. A case of this kind arises for example in the treatment of weighed silk fibres with glycerine stearic ester, to which some potash soap has been added. Silk, cotton and wool yarns can be treated with ease with these esters or mixtures or solutions thereof, 'I'hey thereby obtain 'a strength and suppleness which has ne'verpreviously been attamed, so that thread breakage's, which frequently occurred during the weaving process, are almost completely obviated.
' Moreover the dyeing properties of textile fab- I can thus be more uniformly dyed. Natural silk. is in certain circumstances liable to attack by the atmosphere as soon as it is weighted with tin. If however, it is steeped with the esters derived under the present invention from fatty acids of high molecular weight and polyhydric alcohols,
it becomes much more stable. A further advantage resides'in the fact that raw silk prepared in this way leaves no spots after being worked up. Mediocre silks are rendered more stable, so that a larger field of use is open to them.
A further sphere of application of these esters resides in their additionto oil-colors. Inthis case they prevent the pigment settling out when the paint is allowed to stand. For example, if glycol-monostearic ester is added to the customary red lead linseed oil paint, even 1.5 per cent is suillcient to prevent the settling-out of the pigment, without the paint being detrimentally influenced thereby.
What I claim is: g l
1. A process for the production of emulsions,
.in which ethereal poly-compounds of at least substances having an alkaline reaction.
2. Aprocess for the production of emulsions,
in which polyhydric alcohols partially esterifled with any derivatives of fatty acids of high molecular weightand particularly their hydroxyare emulsified with water or aqueous solutions of any substances in the presence of small amounts of substances having an alkaline reaction.
3. A process for the production of emulsions, in which ethereal poly-compounds of at least one polyhydric alcohol partially esterified with acids selected'from a group consisting of fatty acids acids, are emulsified with water or aqueous solutions of any substances in the presence of small amounts of substances having an alkaline reaction. Y
4. In the production of emulsions, the process which comprises emulsifying in the presence of small amounts of alkaline reacting substances, ethereal poly-compounds of at least one polyhydric alcohol, partially esterified with high molecular fatty acids, with water and with oleaginous matter selected from a class consisting of fats, fatty acids, waxes, vegetable oils and mineral oils.
5. In the production of emulsions, the process which comprises reacting alkyline oxids with fatty acids of high molecular weight in the presence of an aqueous solution of alkali salts of said fatty acids as catalysts, thereby producing a mixture of partially esterified glycol esters and alkali oleaginous'matter selected from a class consisting of fatty acids, naturalfats and fatty acid containing oils in the presence of an aqueoussolution of alkali salts of said fatty acids as catalysts, thereby producing a mixture of partially esterified glycol esters and alkali salts of said fatty acids, and emulsifying the said resulting mixture with water or aqueous solutions of suitable substances.
' 7. As a new composition of matter, an emulsion comprising water, polyhydric alcohols partially esterified with acids selected from a class consisting of derivatives of fatty acids of high molecular weight, .hydroxy-compounds of said fatty acids and unsaturated derivatives of said fatty acids; and'also containing small amounts of substances of alkaline reaction.
8. As a new composition of matter, an emulsion comprising water, polyhydric alcohols, partially esterified with acids selected from a class consisting of derivatives of fatty acids of high molecular weight, hydroxy-compounds of said fatty acids and unsaturated derivatives of .said fatty acids;
oleaginous matter selected from a class consisting of fatty acids, waxes, natural fats and oils; and also containing small amounts of substances of alkaline reaction.
9. The process of forming an emulsion of oil with water which comprises incorporating there I with an emulsifying agent consisting essentially of polyhydric alcohols partially esterified with higher fatty acids and a quantity of soap suflicient to increase materially the stability of the emulwith water which comprises incorporating therewith an emulsifying agent consisting essentially of ethereal poly-compounds of at least one polyhydric alcohol partially esteriiled with fatty acids of high molecular weight and a quantity of soap sufllcient to increase materially the stability of the emulsion, but not substantially in excess of ten percent based on the weight of the ethereal polycompounds.
quantity of soap suflicient. to increase materially the stability of the emulsion, but not substantially in excess of ten per cent based on the weight of the partially esterifled polyhydric alcohols.
12. Theprocess of forming an emulsion of oilwith water which comprises incorporating therewith an emulsifying agentconsisting essentially of ethereal poly-compounds of at least one polyhydric alcohol partially esterified with acids se-' lected from a group consisting of derivatives of fatty acids of high molecular weight, hydroxycompounds of said fatty acids and umaturated derivatives of said fatty acids and a quantity of soap suilicient to increase materially the stability of the emulsion, but not substantially in excess 5 ,of ten per cent based onthe weight of the p ym 13. In the production of oleaginous emulsions, the process which comprises emulsifying oleaginous matter selected from a classcomistingoffats. l0 fatty acids, waxes, vegetable oils and mineral oils,
,with water and with an emulsifying agent consisting essentially of ethereal poly-compounds of atleast one polyhydric alcohol, partially esteriiled with high molecular weight fatty acids and'a l5 quantity of soap sufllcientto increase materially. the stability of the emulsion, but not substantially in excess of ten per cent based on the weight of the ethereal poly-compounds. Y
14, As a new composition of matter, an emul- 20 sion comprising oil, water; polyhydric alcohols partially esterlfled with acidsgelected from a class fatty acids and unsaturated derivatives of said' fatty acids; and also containing soap in amount sumcient to m, materially the stabflity of the emulsion, but not substantially in excess of ten per cent bas'ed'on the weight of the partially 15. As a new composition of matter, an emulsion comprising water, polyhydric alcohols par tiaily esterli'ied with acids selected from a class consisting of derivatives of fatty acids and unsaturated derivatives of said fatty acids; oleaginous matter selected ,from a class consisting of fatty acids, waxes, natural fats and oils; and also containing soap in amount suilicient to increase materially the stability of the emulsion. but not substantially in excess of ten'per cent based on the w isht oi the partially esterifled polyhydric alcohols.-
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4440654A (en) 1981-04-04 1984-04-03 Henry Zimzik Cooling emulsion and method of producing a cooling emulsion

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4440654A (en) 1981-04-04 1984-04-03 Henry Zimzik Cooling emulsion and method of producing a cooling emulsion

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