US3052562A - Stable emulsions - Google Patents
Stable emulsions Download PDFInfo
- 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
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- 239000000839 emulsion Substances 0.000 title claims description 40
- -1 ETHYL HEXYL Chemical class 0.000 claims description 18
- 150000002148 esters Chemical class 0.000 claims description 18
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 14
- 239000000194 fatty acid Substances 0.000 claims description 14
- 229930195729 fatty acid Natural products 0.000 claims description 14
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 11
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 11
- 239000012071 phase Substances 0.000 claims description 11
- 229910019142 PO4 Inorganic materials 0.000 claims description 10
- 239000010452 phosphate Substances 0.000 claims description 10
- 235000010354 butylated hydroxytoluene Nutrition 0.000 claims description 9
- 239000008346 aqueous phase Substances 0.000 claims description 8
- RDOFJDLLWVCMRU-UHFFFAOYSA-N Diisobutyl adipate Chemical compound CC(C)COC(=O)CCCCC(=O)OCC(C)C RDOFJDLLWVCMRU-UHFFFAOYSA-N 0.000 claims description 7
- 229920001214 Polysorbate 60 Polymers 0.000 claims description 7
- 229940031769 diisobutyl adipate Drugs 0.000 claims description 7
- 150000004665 fatty acids Chemical class 0.000 claims description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000000123 paper Substances 0.000 description 36
- 239000003963 antioxidant agent Substances 0.000 description 34
- 230000003078 antioxidant effect Effects 0.000 description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 239000003921 oil Substances 0.000 description 12
- 235000019198 oils Nutrition 0.000 description 12
- 239000000203 mixture Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- 235000013305 food Nutrition 0.000 description 8
- 239000011087 paperboard Substances 0.000 description 8
- 235000010290 biphenyl Nutrition 0.000 description 7
- 239000004305 biphenyl Substances 0.000 description 7
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 6
- 229920000053 polysorbate 80 Polymers 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 5
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 235000014121 butter Nutrition 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 241000209149 Zea Species 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 229920000136 polysorbate Polymers 0.000 description 2
- 238000001256 steam distillation Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000001149 (9Z,12Z)-octadeca-9,12-dienoate Substances 0.000 description 1
- WTTJVINHCBCLGX-UHFFFAOYSA-N (9trans,12cis)-methyl linoleate Natural products CCCCCC=CCC=CCCCCCCCC(=O)OC WTTJVINHCBCLGX-UHFFFAOYSA-N 0.000 description 1
- LNJCGNRKWOHFFV-UHFFFAOYSA-N 3-(2-hydroxyethylsulfanyl)propanenitrile Chemical compound OCCSCCC#N LNJCGNRKWOHFFV-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- PKIXXJPMNDDDOS-UHFFFAOYSA-N Methyl linoleate Natural products CCCCC=CCCC=CCCCCCCCC(=O)OC PKIXXJPMNDDDOS-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- VSYMNDBTCKIDLT-UHFFFAOYSA-N [2-(carbamoyloxymethyl)-2-ethylbutyl] carbamate Chemical compound NC(=O)OCC(CC)(CC)COC(N)=O VSYMNDBTCKIDLT-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 230000002009 allergenic effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229960004217 benzyl alcohol Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- BDIFKMOUQSYRRD-UHFFFAOYSA-N diphenyl hexanedioate Chemical compound C=1C=CC=CC=1OC(=O)CCCCC(=O)OC1=CC=CC=C1 BDIFKMOUQSYRRD-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N para-hydroxytoluene Natural products CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP 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
- D21H21/00—Non-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
- D21H21/14—Non-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
- D21H21/36—Biocidal agents, e.g. fungicidal, bactericidal, insecticidal agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/34—Higher-molecular-weight carboxylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, 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
- C11B5/00—Preserving by using additives, e.g. anti-oxidants
- C11B5/0021—Preserving by using additives, e.g. anti-oxidants containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, 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
- C11B5/00—Preserving by using additives, e.g. anti-oxidants
- C11B5/0021—Preserving by using additives, e.g. anti-oxidants containing oxygen
- C11B5/0035—Phenols; Their halogenated and aminated derivates, their salts, their esters with carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, 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
- C11B5/00—Preserving by using additives, e.g. anti-oxidants
- C11B5/0092—Mixtures
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S106/00—Compositions: coating or plastic
- Y10S106/901—Low 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.
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- 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,
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)
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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0313708D0 (en) * | 2003-06-13 | 2003-07-16 | J R Crompton Ltd | Beverage package |
Citations (1)
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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2758032A (en) * | 1951-11-10 | 1956-08-07 | American Cyanamid Co | Antioxidant wrapper for foods |
-
0
- NL NL130711D patent/NL130711C/xx active
- NL NL262873D patent/NL262873A/xx unknown
-
1960
- 1960-03-30 US US18481A patent/US3052562A/en not_active Expired - Lifetime
-
1961
- 1961-03-28 DE DES73202A patent/DE1167174B/en active Pending
- 1961-03-28 FR FR857039A patent/FR1295399A/en not_active Expired
- 1961-03-28 GB GB11312/61A patent/GB904620A/en not_active Expired
Patent Citations (1)
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)
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) |
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