US3052562A - Stable emulsions - Google Patents

Stable emulsions Download PDF

Info

Publication number
US3052562A
US3052562A US18481A US1848160A US3052562A US 3052562 A US3052562 A US 3052562A US 18481 A US18481 A US 18481A US 1848160 A US1848160 A US 1848160A US 3052562 A US3052562 A US 3052562A
Authority
US
United States
Prior art keywords
paper
antioxidant
emulsion
ester
water
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
Application number
US18481A
Inventor
Gerald R Ferrante
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shell USA Inc
Original Assignee
Shell Oil Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to NL130711D priority Critical patent/NL130711C/xx
Priority to NL262873D priority patent/NL262873A/xx
Application filed by Shell Oil Co filed Critical Shell Oil Co
Priority to US18481A priority patent/US3052562A/en
Priority to GB11312/61A priority patent/GB904620A/en
Priority to DES73202A priority patent/DE1167174B/en
Priority to FR857039A priority patent/FR1295399A/en
Application granted granted Critical
Publication of US3052562A publication Critical patent/US3052562A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/36Biocidal agents, e.g. fungicidal, bactericidal, insecticidal agents
    • 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
    • C09K23/34Higher-molecular-weight carboxylic acid esters
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B5/00Preserving by using additives, e.g. anti-oxidants
    • C11B5/0021Preserving by using additives, e.g. anti-oxidants containing oxygen
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B5/00Preserving by using additives, e.g. anti-oxidants
    • C11B5/0021Preserving by using additives, e.g. anti-oxidants containing oxygen
    • C11B5/0035Phenols; Their halogenated and aminated derivates, their salts, their esters with carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B5/00Preserving by using additives, e.g. anti-oxidants
    • C11B5/0092Mixtures
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S106/00Compositions: coating or plastic
    • Y10S106/901Low molecular weight hydrocarbon polymer-containing mixture

Definitions

  • antioxidants The additionof chemical stabilizers, preservatives or antioxidants to organic materials subject to oxidative deterioration is well known.
  • Small amounts of antioxidants have been incorporated into such materials as butter, lard, hydrogenated fats, vegetable oils and the like, as well as into toilet soaps and other non-food items.
  • the antioxidant In the case of foods, of course, the antioxidant must be non-toxic as well as tasteless and non-discoloring.
  • Antioxidants used in such materials as soaps, which contact the human skin must be non-toxic, non-irritating and non allergenic. Thus, severe restrictions apply to properties of chemical antioxidants or oxidation inhibitors which are to be incorporated directly into the organic material to be stabilized.
  • the loss of antioxidant has been found to result not from the volatility of the antioxidant alone but from its steam distillation thereof when wet paper containing the stabilizer is dried under the conditions described. Under the conditions of paper drying, the partial vapor pressure of the relatively non-volatile phenolic antioxidant in the stream is sufficient to effect the rapid removal of the antioxidant from the paper with the removal of the water of manufacture in the paper.
  • Another object is the provision of an economical composition for such purposes which may be conveniently used in papermaking. Still another object is the provision of a process for employing the antioxidant compositions of the invention. Other objects will be clear from the following description of the invention. Another object is the provision of an emulsion which is unusually easy to prepare and is remarkably stable.
  • a stable aqueous emulsion consisting of a continuous aqueous phase having dispersed therein an oil phase consisting of a waterdmmiscible ester selected from the group consisting of diisobutyl phthalate and ethyl hexyl diphenyl phosphate, up to by weight, based on the ester, of 2,6-di-tert-butyl-4-methylphenol, and up to 100% by weight, based on the phenol, of a fatty acid ester of polyoxyethylene sorbitan.
  • This emulsion has the advantage of being very easily prepared, extremely stable, and being entirely composed of components which are safe for human consumption.
  • the 2,6-di-tert butyl-4-methylphenol is employed in the composition of the invention as a solute in a special type of non-volatile ester.
  • This type of ester has been approxed for food packaging by the US. Food and Drug Administration and is selected from diisobutyl adipate and ethyl hexyl diphenyl phosphate.
  • diisobutyl adipate and ethyl hexyl diphenyl phosphate In addition to being suitable for food uses, both of these esters have extremely low vapor pressure at relatively high temperature.
  • the boiling point and vapor pressure of ethyl hexyl diphenyl phosphate for example, are shown in the following table:
  • This compound is also known as butylat-' White Ethyl Corn Refined Hexyl Diisobutyl Oil Mineral Diphenyl Adipate Oil Phosphate 2,6-(li-tert-butyl 4-metl1yl- 30 30 60 80 phenol solubility at 21 C. (g./100 g.).
  • the ester solution of 2,6-di-tert-butyl-4-methylphenol is dispersed in water to form the emulsion of the invention.
  • the dispersion may be accomplished by any of the means known to the art, such as shakers, stirrers, colloid mills and the like.
  • the amount of water employed for the dispersion is, of course, at least that required to form a continuous phase and may be as little as by volume, based on the ester. The quantity of water required will, however, depend on such variables as the temperature of the dispersion and the nature of the emulsifying agent employed.
  • an ester-miscible emulsifier is employed.
  • These emulsifiers are selected from the polyoxyethylene sorbitan esters of fatty acids having 12 to 18 carbon atoms.
  • Example of such esters include polyoxyethylene sorbitant monolaurate, polyoxyethylene sorbitant monopalmitate, polyoxyethylene sorbitan monostearate, and polyoxyethylene sorbitan monooleate.
  • polyoxyethylene sorbitan monooleate that which has been found to afford the most stability is polyoxyethylene sorbitan monooleate, and it is therefore the preferred emulsifier.
  • emulsifier may be employed in a concentration of up to 100% by weight, based on the weight of 2,6-di-tertbutyl-4-methylphenol in the emulsion, about 1030% by weight has been found to be sufficient under most conditions.
  • One principal advantage of the emulsions of the invention is the ease with which they are formed. It has been unexpectedly found that merely by adding the ester solution containing the phenol and emulsifier to water and stirring the mixture extremely stable oil-in-water emulsions are almost instantly formed. These emulsions are not broken upon heating, dilution, or agitation, and thus are particularly suitable for use under industrial conditions where ease of prepartion and considerable stability are desired.
  • Such an emulsion aifords a useful concentrate which can be prepared, stored and transported without breaking, and which may be readily diluted with additional water prior to use.
  • the diluted emulsion in any desired concentration, is applied to paper by rolling, brushing or spraying the prepartion onto the moving sheet. Since the sheet will then contain the Water from the continuous phase of the emulsion as well as water from the papermaking process itself, the water is best removed by passing the sheet to the drying section of the papermaking machine and driving off the water at that stage.
  • paper in this description is meant not only unwaxed paper and glassine paper but also waxed papers wherein the emulsion may be 'added to the paper prior to coating, and paperboard including waxed paperboard and such nnwaxed board as chocolate board.
  • the use of the emulsion described with these types of paper and paperboard will in no way limit the incorporation in or on the paper or board of conventional paper additives, such as wax; glue, starch and other sizes; clay, talc, chalk and other fillers; titanium or zinc oxides and other pigments; and inks or other coatings.
  • the paper packaging materials prepared with the emulsion described may be used alone or with a protective outer wrapping of cellophane, metal foil such as aluminum foil, synthetic organic resins such as polyethylene or polystyrene, and the like.
  • Example I An oil-in-water emulsion was prepared in which the oil phase had the following composition:
  • the emulsion was prepared by mixing a colloid mill at 60 C., the emulsion was still stable and unbroken after nine months standing at room temperature.
  • the second organic antioxidant solution had the following composition:
  • aqueous emulsions formed by the mill were considerably less stable than those prepared from the first solution, breaking after about one-half the storage time.
  • a stable aqueous emulsion consisting of a continuous aqueous phase having dispersed therein an oil phase consisting of a water-immiscible ester selected from the group consisting of diisobutyl adipate and ethyl hexyl diphenyl phosphate, from about 60% to 100% by weight, based on the ester, of 2,6-di-tert-butyl-4-methylphenol, and from about to 100% by weight, based on the phenol, of a fatty acid ester of polyoxyethylene sorbitan, said fatty acid having from 12 to 18 carbon atoms.
  • a stable aqueous emulsion consisting of a continuous aqueous phase having dispersed therein an oil phase consisting of diisobutyl adipate, from about 60% to 100% 6 by weight, based on the adipate, of 2,6-di-tert-butyl-4- methylphenol, and from about 10% to 100% by weight, based on the phenol, of a fatty acid ester of polyoxyethylene sorbitan, said fatty acid having from 12 to 18 carbon atoms.
  • a stable aqueous emulsion consisting of a continuous aqueous phase having therein an oil phase consisting of ethyl hexyl diphenyl phosphate, from about to by Weight, based on the phosphate, of 2,6-di-tert-buty1- 4-methylphenol, and from about 10% to 100% by weight, based on the phenol, of a fatty acid ester of polyoxyethylene sorbitan, said fatty acid having from 12 to 18 carbon atoms.
  • a stable aqueous emulsion consisting of a continuous aqueous phase having therein an oil phase consisting of 50% by weight of diisobutyl adipate, 40% by weight of 3,5-di-tert-butyl-4-rnethylphenol, and 10% by weight of polyoxyethylene sorbitan monooleate.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Pest Control & Pesticides (AREA)
  • Materials Engineering (AREA)
  • Paper (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

United States Patent ()fifice 3,52,562- Patented Sept. 4, i962 3,052,562 STABLE EMULSIGNS Gerald R. Ferrante, Metuchen, NJL, assignor to Shell Oil Company, New York, N.Y., a corporation of Delaware No Drawing. Filed Mar. 30, 1960, Ser. No. 18,481 6 Claims. (Cl. l06287) This invention relates to antioxidant compositions useful in papermaking and to a process for employing such emulsions in paper manufacturing. More particularly, it relates to novel antioxidant emulsions and their application to paper during manufacture.
The additionof chemical stabilizers, preservatives or antioxidants to organic materials subject to oxidative deterioration is well known. Small amounts of antioxidants have been incorporated into such materials as butter, lard, hydrogenated fats, vegetable oils and the like, as well as into toilet soaps and other non-food items. In the case of foods, of course, the antioxidant must be non-toxic as well as tasteless and non-discoloring. Antioxidants used in such materials as soaps, which contact the human skin, must be non-toxic, non-irritating and non allergenic. Thus, severe restrictions apply to properties of chemical antioxidants or oxidation inhibitors which are to be incorporated directly into the organic material to be stabilized.
In most organic materials packaged in solid form, such as butter or soap, oxidative attack occurs mostly at the surface of the material. As a consequence, it is more important to provide the antioxidant at the surface than in the bulk of the packaged item. Thus, more economical use of the antioxidant can be made if the antioxidant is employed only at that surface. This employment is conventionally carried out by incorporating the antioxidant in the paper packaging surrounding and in contact with the packaged item. Since it is known that paper, or traces of chemicals in the paper, catalyze the oxidation of fats and oils, the inclusion of antioxidant in the paper serves both to protect the packaged item in general and to repress the oxidative effect of the paper in particular. Since in oily materials, such as butter, oil leached from the packaged item into the packaging paper tends to turn rancid rapidly because of the nature and extended surface of the paper, the incorporation of antioxidant in the paper also prevents such rancidity from developing.
A variety of methods have been employed for impregnating paper with antioxidants. Typical methods include the addition to the paper of antioxidant emulsions at the. beater, or as emulsion or solutions to the finished sheet leaving the Fourdrinier machine. The latter type of application may be accomplished by passing the sheet through a bath of the antioxidant-containing liquid or by calendering the liquid onto the paper. In either case, the dispersant or solvent liquid must be removed from the paper sheet in the course of manufacture. Such removal is generally accomplished by passing the paper over steam-heated dryer rolls which remove not only much of the water in the moving sheet but also any other volatile liquids which have been added to the paper in the course of manufacture.
It has been observed that serious antioxidant losses occur when impregnated papers containing conventional phenolic stabilizers are passed through heated drying sections of papermaking machines. Losses as great as 90% of the added stabilizer have been measured. As a consequence, to obtain given concentrations of antioxidant in certain papers, ten times as much of the com pound must be added thereto. Since antioxidants are generally expensive chemicals, losses on such a scale seriously increase the cost of the impregnated paper.
The loss of antioxidant has been found to result not from the volatility of the antioxidant alone but from its steam distillation thereof when wet paper containing the stabilizer is dried under the conditions described. Under the conditions of paper drying, the partial vapor pressure of the relatively non-volatile phenolic antioxidant in the stream is sufficient to effect the rapid removal of the antioxidant from the paper with the removal of the water of manufacture in the paper.
It has been found that by employing the antioxidant in the form of an emulsion in certain non-volatile Waterimmiscible liquids the loss of antioxidant by steam distillation is effectively prevented. As a consequence, it is an object of this invention to provide an antioxidant composition which, when employed in paper, will reduce or prevent loss of the antioxidant. A further object is the provision of a non-toxic antioxidant composition which may be employed in paper used in the packagingof.
foods, soap and other items intended for human consumption and use. The provision of an economical composition for such purposes which may be conveniently used in papermaking is another object of the invention. Still another object is the provision of a process for employing the antioxidant compositions of the invention. Other objects will be clear from the following description of the invention. Another object is the provision of an emulsion which is unusually easy to prepare and is remarkably stable.
These objects are accomplished in the invention by a stable aqueous emulsion consisting of a continuous aqueous phase having dispersed therein an oil phase consisting of a waterdmmiscible ester selected from the group consisting of diisobutyl phthalate and ethyl hexyl diphenyl phosphate, up to by weight, based on the ester, of 2,6-di-tert-butyl-4-methylphenol, and up to 100% by weight, based on the phenol, of a fatty acid ester of polyoxyethylene sorbitan. This emulsion has the advantage of being very easily prepared, extremely stable, and being entirely composed of components which are safe for human consumption.
Of the many phenolic antioxidants known, one of the most effective single compounds is 2,6-di-tert-butyl-4- methylphenol. ed hydroxytoluene and as di-tert-butyl-p-cresol. Because it is one of the few synthetic chemical compounds approved for antioxidant use in foods by the Food and Drug Administration, it is employed extensively in foods and food packaging.
The 2,6-di-tert butyl-4-methylphenol is employed in the composition of the invention as a solute in a special type of non-volatile ester. This type of ester has been approxed for food packaging by the US. Food and Drug Administration and is selected from diisobutyl adipate and ethyl hexyl diphenyl phosphate. In addition to being suitable for food uses, both of these esters have extremely low vapor pressure at relatively high temperature. The boiling point and vapor pressure of ethyl hexyl diphenyl phosphate, for example, are shown in the following table:
Temperature, C
Vapor pressure abs, mm. Hg
This compound is also known as butylat-' White Ethyl Corn Refined Hexyl Diisobutyl Oil Mineral Diphenyl Adipate Oil Phosphate 2,6-(li-tert-butyl 4-metl1yl- 30 30 60 80 phenol solubility at 21 C. (g./100 g.).
From these data it will be apparent that far more of the antioxidant can be incorporated in paper with a given amount of the esters of this invention than can be when corn or mineral oil is employed.
The ester solution of 2,6-di-tert-butyl-4-methylphenol is dispersed in water to form the emulsion of the invention. The dispersion may be accomplished by any of the means known to the art, such as shakers, stirrers, colloid mills and the like. The amount of water employed for the dispersion is, of course, at least that required to form a continuous phase and may be as little as by volume, based on the ester. The quantity of water required will, however, depend on such variables as the temperature of the dispersion and the nature of the emulsifying agent employed.
To stabilize the oil-in-water dispersion of the ester containing the antioxidant in the Water, an ester-miscible emulsifier is employed. These emulsifiers are selected from the polyoxyethylene sorbitan esters of fatty acids having 12 to 18 carbon atoms. Example of such esters include polyoxyethylene sorbitant monolaurate, polyoxyethylene sorbitant monopalmitate, polyoxyethylene sorbitan monostearate, and polyoxyethylene sorbitan monooleate. Of these esters, that which has been found to afford the most stability is polyoxyethylene sorbitan monooleate, and it is therefore the preferred emulsifier. While the emulsifier may be employed in a concentration of up to 100% by weight, based on the weight of 2,6-di-tertbutyl-4-methylphenol in the emulsion, about 1030% by weight has been found to be sufficient under most conditions.
One principal advantage of the emulsions of the invention is the ease with which they are formed. It has been unexpectedly found that merely by adding the ester solution containing the phenol and emulsifier to water and stirring the mixture extremely stable oil-in-water emulsions are almost instantly formed. These emulsions are not broken upon heating, dilution, or agitation, and thus are particularly suitable for use under industrial conditions where ease of prepartion and considerable stability are desired.
Such an emulsion aifords a useful concentrate which can be prepared, stored and transported without breaking, and which may be readily diluted with additional water prior to use. In practice, the diluted emulsion, in any desired concentration, is applied to paper by rolling, brushing or spraying the prepartion onto the moving sheet. Since the sheet will then contain the Water from the continuous phase of the emulsion as well as water from the papermaking process itself, the water is best removed by passing the sheet to the drying section of the papermaking machine and driving off the water at that stage.
By paper in this description is meant not only unwaxed paper and glassine paper but also waxed papers wherein the emulsion may be 'added to the paper prior to coating, and paperboard including waxed paperboard and such nnwaxed board as chocolate board. The use of the emulsion described with these types of paper and paperboard will in no way limit the incorporation in or on the paper or board of conventional paper additives, such as wax; glue, starch and other sizes; clay, talc, chalk and other fillers; titanium or zinc oxides and other pigments; and inks or other coatings. Furthermore, the paper packaging materials prepared with the emulsion described may be used alone or with a protective outer wrapping of cellophane, metal foil such as aluminum foil, synthetic organic resins such as polyethylene or polystyrene, and the like.
The following examples will illustrate the nature and advantages of the invention. It should be understood, however, that the examples are merely illustrative and are not to be regarded as limitations to the appended claims since the basic teachings thereof may be varied at will as will be understood by one skilled in the art.
Example I An oil-in-water emulsion was prepared in which the oil phase had the following composition:
Parts by weight 2,6-di-tert-butyl-4-methylphenol 10.0 Diisobutyl phthalate 12.5 Tween (polyoxyethylene sorbitan monooleate) 2.5
Total 25.0
This ester solution was stirred into water until the total emulsion contained 6% w. of the phenol in the organic dispersed phase. The emulsion formed readily on handstirring.
Similar emulsions are formed by substituting ethyl hexyl diphenyl phosphate.
In a plant run, twelve tons of paperboard were impregnated with the emulsion, the level of impregnation being about two pounds of the phenol per ton of paperboard.
Samples of the paperboard were taken at various times during the run, and a sample of the emulsion was analyzed at the beginning of the run. Resulting data are presented in the following table:
test. In the test, 0.2 gram of paperboard, immersed in 1.0 gram of methyl linoleate, was stored in an oven at 50 C. The sample was weighed daily and when an increase of 12 mg. was obtained, the sample was considered rancid. Results of the test are given below.
Sample Days to Rancidity at 50 C.
N o paperboard 7 Untreated board 3% Initial board 5% Middle board 8 Final board 5% Example 11 Two 10-ml. samples of organic antioxidant solutions were emulsified. The first solution had the following composition:
Parts by weight 2,6-di-tert-buty l-4-methylphenol 10 Diisobutyl adipate 12.5
Tween 80 (polyoxyethylene sorbitan monooelate) 2.5
Total 25.0
This solution was added to about 250 ml. of water and the mixture was stirred gently with a glass stirring rod. A white emulsion quickly formed which was still stable and unbroken after standing ninety days at room temperature.
When the emulsion was prepared by mixing a colloid mill at 60 C., the emulsion was still stable and unbroken after nine months standing at room temperature.
Further experiments showed that the aqueous emulsion could be quickly formed with all proportions of organic and aqueous phases merely by gentle hand stirring.
The second organic antioxidant solution had the following composition:
Volume percent When this solution was added to 250 ml. of water, under the above conditions, no stable emulsion could be formed by hand stirring or stirring with a conventional laboratory stirrer. The emulsion formed by such stirring broke as soon as stirring was stopped. In order to form stable emulsions, violet agitation in a colloid mill for about a half hour was required.
The aqueous emulsions formed by the mill were considerably less stable than those prepared from the first solution, breaking after about one-half the storage time.
I claim as my invention:
1. A stable aqueous emulsion consisting of a continuous aqueous phase having dispersed therein an oil phase consisting of a water-immiscible ester selected from the group consisting of diisobutyl adipate and ethyl hexyl diphenyl phosphate, from about 60% to 100% by weight, based on the ester, of 2,6-di-tert-butyl-4-methylphenol, and from about to 100% by weight, based on the phenol, of a fatty acid ester of polyoxyethylene sorbitan, said fatty acid having from 12 to 18 carbon atoms.
2. A stable aqueous emulsion consisting of a continuous aqueous phase having dispersed therein an oil phase consisting of diisobutyl adipate, from about 60% to 100% 6 by weight, based on the adipate, of 2,6-di-tert-butyl-4- methylphenol, and from about 10% to 100% by weight, based on the phenol, of a fatty acid ester of polyoxyethylene sorbitan, said fatty acid having from 12 to 18 carbon atoms.
3. A stable aqueous emulsion consisting of a continuous aqueous phase having therein an oil phase consisting of ethyl hexyl diphenyl phosphate, from about to by Weight, based on the phosphate, of 2,6-di-tert-buty1- 4-methylphenol, and from about 10% to 100% by weight, based on the phenol, of a fatty acid ester of polyoxyethylene sorbitan, said fatty acid having from 12 to 18 carbon atoms.
4. The emulsion of claim 2 wherein the fatty acid ester is polyoxyethylene sorbitan monooleate.
5. A stable aqueous emulsion consisting of a continuous aqueous phase having therein an oil phase consisting of 50% by weight of diisobutyl adipate, 40% by weight of 3,5-di-tert-butyl-4-rnethylphenol, and 10% by weight of polyoxyethylene sorbitan monooleate.
6. A process for impregnating paper with an antioxidant, comprising applying to the paper an aqueous emulsion consisting of a continuous aqueous phase having dispersed therein an oil phase consisting of a water-immisci- =b'le ester selected from the group consisting of diisobutyl adipate and ethyl hexyl diphenyl phosphate, from about 30% to 100% by weight, based on the ester, of 2,6-ditert-butyl-4-methylpheno1, and from about 10% to 100% by weight, based on the phenol, of a fatty acid ester of a fatty acid ester of polyoxyethylene sorbitan, said fatty acid having from 12 to 18 carbon atoms.
Atlas Surface Active Agents, 1948, ATL CD-41, 10-48, page 15.
Schwartz et al.: 209.
Surface Active Agents, 1949, page

Claims (1)

1. A STABLE AQUEOUS EMULSION CONSISTING OF A CONTINUOUS AQUEOUS PHASE HAVING DISPERSE THEREIN AN OIL PHASE CONSISTING OF A WATER-IMMISCIBLE ESTER SELECTED FROM THE GROUP CONSISTING OF DIISOBUTYL ADIPATE AND ETHYL HEXYL DISPHENYL PHOSPHATE, FROM ABOUT 60% TO 100% BY WEIGH, BASED ON THE ESTER, OF 2,6-DI-TERT-BUTYL-4-METHYLPHENOL, AND FROM ABOUT 10% TO 100% BY WEIGHT, BASED ON THE PHENOL, OF A FATTY ACID ESTER OF POLYOXYETHYLENE SORBITAN, SAID FATTY ACID HAVING FORM 12 TO 18 CARBON ATOMS,
US18481A 1960-03-30 1960-03-30 Stable emulsions Expired - Lifetime US3052562A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
NL130711D NL130711C (en) 1960-03-30
NL262873D NL262873A (en) 1960-03-30
US18481A US3052562A (en) 1960-03-30 1960-03-30 Stable emulsions
GB11312/61A GB904620A (en) 1960-03-30 1961-03-28 Stable antioxidant emulsions for use in paper manufacture
DES73202A DE1167174B (en) 1960-03-30 1961-03-28 Emulsion for the production of packaging paper containing antioxidants
FR857039A FR1295399A (en) 1960-03-30 1961-03-28 stable antioxidant emulsions for papermaking

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US18481A US3052562A (en) 1960-03-30 1960-03-30 Stable emulsions

Publications (1)

Publication Number Publication Date
US3052562A true US3052562A (en) 1962-09-04

Family

ID=21788147

Family Applications (1)

Application Number Title Priority Date Filing Date
US18481A Expired - Lifetime US3052562A (en) 1960-03-30 1960-03-30 Stable emulsions

Country Status (5)

Country Link
US (1) US3052562A (en)
DE (1) DE1167174B (en)
FR (1) FR1295399A (en)
GB (1) GB904620A (en)
NL (2) NL262873A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3296065A (en) * 1963-10-07 1967-01-03 Monsanto Co Paper products containing carboxylic acid esters and process for preparing such products
US3390098A (en) * 1964-06-08 1968-06-25 Armour Pharma Antioxidant composition
US5041485A (en) * 1989-08-03 1991-08-20 Bayer Aktiengesellschaft Stabilizer dispersions
US20050025871A1 (en) * 2003-06-17 2005-02-03 Shoshan Legi Gil Spreadable butter product

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0313708D0 (en) * 2003-06-13 2003-07-16 J R Crompton Ltd Beverage package

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2843497A (en) * 1955-02-23 1958-07-15 Eastman Kodak Co Wax coatings containing synergistic antioxidants

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2758032A (en) * 1951-11-10 1956-08-07 American Cyanamid Co Antioxidant wrapper for foods

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2843497A (en) * 1955-02-23 1958-07-15 Eastman Kodak Co Wax coatings containing synergistic antioxidants

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3296065A (en) * 1963-10-07 1967-01-03 Monsanto Co Paper products containing carboxylic acid esters and process for preparing such products
US3390098A (en) * 1964-06-08 1968-06-25 Armour Pharma Antioxidant composition
US5041485A (en) * 1989-08-03 1991-08-20 Bayer Aktiengesellschaft Stabilizer dispersions
US20050025871A1 (en) * 2003-06-17 2005-02-03 Shoshan Legi Gil Spreadable butter product

Also Published As

Publication number Publication date
NL262873A (en)
DE1167174B (en) 1964-04-02
GB904620A (en) 1962-08-29
FR1295399A (en) 1962-06-08
NL130711C (en)

Similar Documents

Publication Publication Date Title
EP1608707B1 (en) Process for the application of aqueous wax emulsions
US3116305A (en) Hydroxybenzyl esters
EP0292975B1 (en) Sizing pulp
US3052562A (en) Stable emulsions
EP0220941A1 (en) Paper sizing composition
US2843497A (en) Wax coatings containing synergistic antioxidants
JPH0144270B2 (en)
US2320644A (en) Wax composition
US2758032A (en) Antioxidant wrapper for foods
US3097131A (en) Eutectic liquid preservatives
US2500543A (en) Antioxidant
US2803612A (en) 9-octadecenamide-polyethylene compositions
US3052553A (en) Transparent food wrapper
US2086903A (en) Grease repellant paper
US2324529A (en) Manufacture of paper and board
US2155731A (en) Paper treatment
US2636002A (en) Paraffin wax compositions
US2387157A (en) Emulsified petroleum products
US2694014A (en) Paraffin wax compositions
US2485640A (en) Stabilized glyceridic oil compositions and processes of preparing them
US2637665A (en) Impregnated paper and method of making same
US2377359A (en) Manufacture of antioxygenic paper
US2325624A (en) Treatment of paper and paperboard
US2636003A (en) Paraffin wax compositions
US2646362A (en) Paraffin wax composition