US2773812A - Wax composition - Google Patents

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US2773812A
US2773812A US43054754A US2773812A US 2773812 A US2773812 A US 2773812A US 43054754 A US43054754 A US 43054754A US 2773812 A US2773812 A US 2773812A
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wax
composition
oil
solvent
viscosity
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John D Tench
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Sunoco Inc
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Sun Oil Co
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
    • A23C19/00Cheese; Cheese preparations; Making thereof
    • A23C19/14Treating cheese after having reached its definite form, e.g. ripening, smoking
    • A23C19/16Covering the cheese surface, e.g. with paraffin wax
    • A23C19/163Covering the cheese surface, e.g. with paraffin wax with a non-edible liquid or semi-liquid coating, e.g. wax, polymer dispersions
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06Waxes
    • C08L91/08Mineral waxes
    • 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
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31801Of wax or waxy material

Definitions

  • This invention relates ⁇ to Va novel wax composition and more particularly relates to a solid. composition containing paraffin wax, microcrystalline waxand-oil, the composition being especially suitable for coating containers for packaging dairy products.
  • waxes and wax compositions heretofore described as suitable for coating containers for dairy products arenot suitable for certain applications such as coating containers designed to package cottage cheese. It appears thatone or more of the components of cottage'cheese, in some manner, passes through the wax barrier so. that. there after iiuids of the cheese composition can pass through the wax coating. The uids are then absorbed by the iibrous walls of the container, which becomes soggy. The sospoiled container meets considerable consumer resistance, and in some instances leaks develop in the container.
  • Wax for coating such compositions is complicated by the requirement that the waxed-coated containers, when stacked in nesting relation, must not stick together at temperatures ordinarily encountered during storage and shipment, i. e., the blocking temperature of the wax must be relatively high.
  • An object of the present invention is to provide a novel wax composition, made from petroleum hydrocarbons, which is especially suitable for coating containers. Another object is to provide containers for packaging dairy products which will not stick together. when stored in contact at temperatures of up to 100 F., and preferably will not stick when stored in contact at temperatures up to 105 F. A further specic object is to provide ak container for packaging cottage cheese.
  • composition is especially suitable for coatingV fibrous containers, and particularly fibrous containers for packaging cottage cheese.
  • the three components that are combined to produce the composition of the invention are Va paraiiin wax, a microcrystalline wax and a lubricating oil, each of which has specific properties within narrow ranges, as hereinafter deiined. It is essential to the invention that, in parts by weight, from 60 to 70 parts of the parain wax, from 2O to 35 parts of the microcrystalline wax, and from 2 to parts of the oil be employed, as will appear hereinafter.
  • the paraffin wax is prepared by distilling slack wax, or its equivalent, and collecting the light'distillate frac- 2,773,812 Patented Dec. lil, 1956 tion boiling within the range of from about 375 F. to 520 F. at 2 mm. of. mercury pressure. then dissolved in a solvent at an elevated temperature. The resulting solution is cooled to a temperature of from about 30 to 50 F., preferably from about 35 F. to 40 F., when using a mixture of about equal parts by volume of benzene and methyl ethyl ketone as the solvent, or to the temperature that gives the same wax fraction, within the stated limits, when usinga different solvent.
  • the wax precipitated at this temperature is separated, preferably by ltering, and after removal separation of solvent forms the paratiin wax of. the present composition.
  • the solvent is conveniently removed by distillation.
  • the resulting parati'in wax has a melting point of about 12S-142 F. (ASTM D87-42), a viscosity of about 35- 42 SUS at 210 F. (ASTM D446-39), an average molecular weight of about 355-400, and a refractive index at 212 F. of from 1.4.19 to 1.423.
  • the microcrystalline wax of the composition of the iuvention is prepared by distilling slack wax to form a residual Wax boiling above about 525 F. at 2 mm. of mercury pressure. This fraction is dissolved in a solvent at an elevated temperature. 'The resulting solution is chilled to a temperature of from about 40 F. to 60 F. when using a mixture of about equal parts by volume of benzene and methyl ethyl ketone as the solvent, or to a temperature that gives the same wax fraction, within the stated limits, when using a dierent solvent. The precipitated wax is separated, preferably by filtration, and is again dissolved in a solvent at an elevated temperature. This solution is then chilled to a temperature of from about F.
  • the resulting microcrystalline wax has a melting point of about 18S-200 F. (ASTM D-127-49), a viscosity of about 81-89 SUS at 210 F. (ASTM D446-39), an average molecular weight of labout 650, and a refractive index at 212 F. of from 1.435 to 1.438.
  • the nal composition of the process containing the paraiiin and microcrystalline waxes andl oil can be decolorized in like manner.
  • filtration in each instance is advantageously accomplished by means of a rotary vacuum lilter having provision for both supplying wash liquid to the filtered wax and subsequent drying by suction.
  • the fresh wash liquid is advantageously of the same composition as the solvent employed for dissolution of the wax, since recovery and recycling problems are thereby simplified.
  • the solvent employed in preparing the components of the composition should have a preferential solvent power for the oil contained in slack wax, should dissolve the wax at relatively high temperatures, and precipitate wax at lower temperatures.
  • a mixture of methyl ethyl ketone and benzenel in approximately equal parts by volume is they preferred solvent, but either of'these components may be replaced, in whole or in part, by other ketones such as methyl butyl ketone or acetone, or hydrocarbons ⁇ and halogenated hydrocarbons such as ethylene dichloride, pentane and hexane, or alcohols such as propyl or the heptyl alcohols.
  • the oil component'offthe compositionof the inventionv is preferably prepared by solvent-refining the residual fraction from the vacuum distillation of crude petroleum, such as by extraction with furfural or propane-phenol solvents, dewaxing the oil such as by chilling in the presence Aof asolvent selected for preferential dissolution of oil, for example, a mixture of methyl ethyl ketone and benzene, and clay-treating the dewaxed oil.
  • An additional distillation step can be included if necessary or desirable to' insure the preparation of oil having the properties hereafter described. It will be understood that the oil component can be obtained using diterent refining steps, or a different sequence of steps, so long as the oil meets the following specifications.
  • the oil component should boil rwithin the lubricating oil range, and have an API gravity of about 18.
  • the oil has a viscosity at 100 F. of about '100 SUS, and more preferably Iabove about 1000 SUS.
  • the oil has Ia viscosity index vof about 90.
  • the oil should, in any event, have an ini- Y tial boiling point of about 600 F., and preferably above 700 F., at atmospheric pressure.
  • the three components of the invention are conveniently blended by heating proper portions thereof, as hereinafter dened, to :a temperature above the melting point of the microcrystalline wax, and stirring the molten mixture so that on solidiiication a homogeneous composition lis obtained.
  • the Wax composition of the invention exhibits two Ibreaks in the cooling curve (ASTM 'D87-42), one at from 160 to 175. F. and a second at from 123 to 139 F.
  • the composition has a penetration (ASTM -D127'49) at 7:7 F. of from 12 to 21, and at 100 F. of from ⁇ 31 to 50, and a viscosity at 210 F. (ASTM D446-5-3) of from 41 to 51.
  • the composition has a blocking temperature of at least 100 F., and preferably above 105 F.
  • the blending was per,- for-med -at a temperature of about 225 F., which lwas suicient to maintain the components in liquid phase.
  • the paran wax was prepared by distilling reduced crude petroleum having a high wax content yand separating the fraction boiling between 375 and 480 F. at 2 mm. pressure. This entire fraction was dissolved in -a solvent consisting of about equal parts of benzene and methyl ethyl ketone at a temperature of about 180
  • the microcrystalline wax was prepared by distilling
  • the recovered Wax is the paraffin Wax employed slack Wax to remove the fractions boiling above about 525 F. Iat 2 mm. pressure.
  • the residue ⁇ was dissolved in a solvent .at .a temperature of about 210 F. and the resulting solution chilled to a temperature of 50 F.
  • Wax compositions having varying quantities of the parain wax, microcrystalline wax and oil, prepared as above described, were compounded and tested as follows: heavy paper stock employed for making cottage cheese containers was cut into strips of about 2 by ⁇ 6 inches. The k strips were dipped finto the molten composition :of the 4in-Vl vention to form a desired weight of Wax per unit area of paper stock. 'I'he coated paper was then cooled to room temperature. Similar strips were coated with waxes heretofore used for coating such containers.
  • compositions blocking at below 100"V F. were considered to fail the test; the compositions that passed the test had n. blocking temperature of atleast F. Y
  • Example 2 Sample C of vExample 1 was duplicated except that the paraffin wax employed had a melting point of F. and an average molecular weight of 385. On testing the composition as described in Example 1, good protection was observed, i. e., a pass was obtained in the protection test, and a pass wasalso obtained in the blocking lest.
  • Example 3 A composition according to Example 2 was prepared except that aV different oilV was used.
  • Other properties were within the limitations as described above.
  • the quantity of parafn Wax to employ must be within the range of from 60-70% by weight
  • the quantity of microcrystalline wax to employ must be within the range of from 25-35% by Weight
  • the quantity of oil to employ must be within the range of from 2-l0% by weight.
  • the preferred composition, with which excellent results are obtained contains 30% by weight of the microcrystalline wax, 65% by weight of the parain wax and 5% by weight of the oil.
  • a new composition of matter comprising: (A) from 60 to 70 parts of a paran wax having a melting point of from about 125 F. to 142 P., a viscosity of about 35 to 42 SUS at 210 F., a refractive index at 212 F. of from 1.419 to 1.423 and an average molecular Weight of from about 355 to about 400; (B) from 25 to 35 parts of a microcrystalline Wax boiling above about 525 F. at 2 mm. mercury pressure, and having a melting point of from about 185 F. to about 200 F., a viscosity at 210 F. of from about 8l to 89 SUS, a refractive index at 212 F. of from 1.435 to 1.438; and (C) from 2 to 10 parts of a lubricating oil having an API gravity of above 18 and an initial boiling point of above 600 F.
  • a new article of manufacture comprising a brous container for packaging dairy products coated with the composition of claim l.
  • Process for the preparation of a new composition of matter which comprises admixing in the molten state: (A) from to 70 parts of a paran wax having a melting point of from about F. to 142 F., a viscosity of about 35 to 42 SUS at 210 F., a refractive index at 212 F. of from 1.419 to 1.423 and an average molecular weight of from about 355 to about 400; (B) from 25 to 35 parts of a microcrystalline wax boiling above about 525 F. at 2 mm. mercury pressure, and having a melting point of from about F. to about 200 F., a viscosity at 210 F. of from about 8l to 89 SUS, a refractive index at 212 F. of from 1.435 to 1.438; and (C) from 2 to l0 parts of a lubricating oil having an API gravity of above 18 and an initial boiling point of above 600 F., and solidifying the molten composition.

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  • Chemical & Material Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
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Description

Dec. 11, 1956 J. D. TENCH 2,773,812
WAX COMPOSITION Filed May 18. 1954 Puroffin Wx A A A vvAv vA vvv v g A 9 o AA AvAvAvA 5% AvAvAvA AvAvAvAvAvvAvAvAvAvA vvvv W vvv @@@QWMM w@ Q www Ko Mmm/Awww oowwvvvvw/mvw/vw vv\/\/\/\/\/\^/\/\/vv\/\/\/V\Oil Microcrysnline Wan INVENTOR.
JOHN o. rl-:NCH
ATTORNEY United StatesV Patent O wax ComosrrfIoN .lohn D. Teach, Prospect Park, Pa., assignor to Sun Oil Company, Philadelphia, Pa., a corporation of New Jersey Application May- 18, 1954,.Serial,No. 430,547'
3 Claims. (Cl. 1945-149) This invention relates `to Va novel wax composition and more particularly relates to a solid. composition containing paraffin wax, microcrystalline waxand-oil, the composition being especially suitable for coating containers for packaging dairy products.
Paraiiin waxes have heretofore been employed for la variety of uses, such as water-proofing textiles and papers. ln order to obtain certain properties for such waxes, foreign materials such as microcrystalline wax, rubber, beeswax, resins, and the like, have been compounded therewith. Such compositions, however, have not proved entirely satisfactory for certain purposes. For example, waxes and wax compositions heretofore described as suitable for coating containers for dairy products arenot suitable for certain applications such as coating containers designed to package cottage cheese. It appears thatone or more of the components of cottage'cheese, in some manner, passes through the wax barrier so. that. there after iiuids of the cheese composition can pass through the wax coating. The uids are then absorbed by the iibrous walls of the container, which becomes soggy. The sospoiled container meets considerable consumer resistance, and in some instances leaks develop in the container.
The provision of a suitable Wax for coating such compositions is complicated by the requirement that the waxed-coated containers, when stacked in nesting relation, must not stick together at temperatures ordinarily encountered during storage and shipment, i. e., the blocking temperature of the wax must be relatively high.
An object of the present invention is to provide a novel wax composition, made from petroleum hydrocarbons, which is especially suitable for coating containers. Another object is to provide containers for packaging dairy products which will not stick together. when stored in contact at temperatures of up to 100 F., and preferably will not stick when stored in contact at temperatures up to 105 F. A further specic object is to provide ak container for packaging cottage cheese.
lt has now been discovered that by compounding three separate components prepared from petroleum, all of which have specic properties within narrow ranges, the
resulting composition is especially suitable for coatingV fibrous containers, and particularly fibrous containers for packaging cottage cheese.
The three components that are combined to produce the composition of the invention are Va paraiiin wax, a microcrystalline wax and a lubricating oil, each of which has specific properties within narrow ranges, as hereinafter deiined. It is essential to the invention that, in parts by weight, from 60 to 70 parts of the parain wax, from 2O to 35 parts of the microcrystalline wax, and from 2 to parts of the oil be employed, as will appear hereinafter.
The accompanying drawing is a ternary diagram showing the permissible variations in the concentrations ofthe three components, as hereinafter described.
The paraffin wax is prepared by distilling slack wax, or its equivalent, and collecting the light'distillate frac- 2,773,812 Patented Dec. lil, 1956 tion boiling within the range of from about 375 F. to 520 F. at 2 mm. of. mercury pressure. then dissolved in a solvent at an elevated temperature. The resulting solution is cooled to a temperature of from about 30 to 50 F., preferably from about 35 F. to 40 F., when using a mixture of about equal parts by volume of benzene and methyl ethyl ketone as the solvent, or to the temperature that gives the same wax fraction, within the stated limits, when usinga different solvent. The wax precipitated at this temperature is separated, preferably by ltering, and after removal separation of solvent forms the paratiin wax of. the present composition. The solvent is conveniently removed by distillation.
The resulting parati'in wax has a melting point of about 12S-142 F. (ASTM D87-42), a viscosity of about 35- 42 SUS at 210 F. (ASTM D446-39), an average molecular weight of about 355-400, and a refractive index at 212 F. of from 1.4.19 to 1.423.
The microcrystalline wax of the composition of the iuvention is prepared by distilling slack wax to form a residual Wax boiling above about 525 F. at 2 mm. of mercury pressure. This fraction is dissolved in a solvent at an elevated temperature. 'The resulting solution is chilled to a temperature of from about 40 F. to 60 F. when using a mixture of about equal parts by volume of benzene and methyl ethyl ketone as the solvent, or to a temperature that gives the same wax fraction, within the stated limits, when using a dierent solvent. The precipitated wax is separated, preferably by filtration, and is again dissolved in a solvent at an elevated temperature. This solution is then chilled to a temperature of from about F. to about 120 F., and preferably about F., when using the benzene-methyl ethyl ketone solvent, or to an equivalent temperature with a different solvent, as above described. The wax precipitated at this temperature is separated from the solution, preferably byV filtration. Separation of solvent'from the wax, such as by distillation, forms the microcrystalline wax of the present composition.
The resulting microcrystalline wax has a melting point of about 18S-200 F. (ASTM D-127-49), a viscosity of about 81-89 SUS at 210 F. (ASTM D446-39), an average molecular weight of labout 650, and a refractive index at 212 F. of from 1.435 to 1.438.
In the preparation of both the paraliin and microcrystalline waxes, it is-advantageous to include a decolorization step, such as by contacting the molten Wax with clay,v but decolorization is not necessary to the successful operation of the invention. If desired, the nal composition of the process containing the paraiiin and microcrystalline waxes andl oil can be decolorized in like manner.
In preparing the wax components of the composition, filtration in each instance is advantageously accomplished by means of a rotary vacuum lilter having provision for both supplying wash liquid to the filtered wax and subsequent drying by suction. The fresh wash liquid is advantageously of the same composition as the solvent employed for dissolution of the wax, since recovery and recycling problems are thereby simplified.
The solvent employed in preparing the components of the composition should have a preferential solvent power for the oil contained in slack wax, should dissolve the wax at relatively high temperatures, and precipitate wax at lower temperatures. A mixture of methyl ethyl ketone and benzenel in approximately equal parts by volume is they preferred solvent, but either of'these components may be replaced, in whole or in part, by other ketones such as methyl butyl ketone or acetone, or hydrocarbons `and halogenated hydrocarbons such as ethylene dichloride, pentane and hexane, or alcohols such as propyl or the heptyl alcohols.
The oil component'offthe compositionof the inventionv This fraction isl ispreferably prepared by solvent-refining the residual fraction from the vacuum distillation of crude petroleum, such as by extraction with furfural or propane-phenol solvents, dewaxing the oil such as by chilling in the presence Aof asolvent selected for preferential dissolution of oil, for example, a mixture of methyl ethyl ketone and benzene, and clay-treating the dewaxed oil. An additional distillation step can be included if necessary or desirable to' insure the preparation of oil having the properties hereafter described. It will be understood that the oil component can be obtained using diterent refining steps, or a different sequence of steps, so long as the oil meets the following specifications.
The oil component should boil rwithin the lubricating oil range, and have an API gravity of about 18. Preferably the oil has a viscosity at 100 F. of about '100 SUS, and more preferably Iabove about 1000 SUS. In the preferred embodiment, the oil has Ia viscosity index vof about 90. The oil should, in any event, have an ini- Y tial boiling point of about 600 F., and preferably above 700 F., at atmospheric pressure.
The three components of the invention are conveniently blended by heating proper portions thereof, as hereinafter dened, to :a temperature above the melting point of the microcrystalline wax, and stirring the molten mixture so that on solidiiication a homogeneous composition lis obtained.
The Wax composition of the invention exhibits two Ibreaks in the cooling curve (ASTM 'D87-42), one at from 160 to 175. F. and a second at from 123 to 139 F. The composition has a penetration (ASTM -D127'49) at 7:7 F. of from 12 to 21, and at 100 F. of from `31 to 50, and a viscosity at 210 F. (ASTM D446-5-3) of from 41 to 51. The composition has a blocking temperature of at least 100 F., and preferably above 105 F.
Example 1 -In 'order to illustrate the compositions of the invention and their process of preparation, there were blended varying quantities of a paralhn wax, a microcrystalline wax `and ya lubricating oil, the .components having properties within the limits given above. The blending was per,- for-med -at a temperature of about 225 F., which lwas suicient to maintain the components in liquid phase.
The paran wax was prepared by distilling reduced crude petroleum having a high wax content yand separating the fraction boiling between 375 and 480 F. at 2 mm. pressure. This entire fraction was dissolved in -a solvent consisting of about equal parts of benzene and methyl ethyl ketone at a temperature of about 180 |F. The resulting solution was cooled to 35 F. and the precipitated wax separated 'by tiltration. The wax cake was washed with the same solvent used -to dissolve the distillate fraction. The wax was separated from the solvent by distillation and subsequently decolorized |by clay contacting. in the present composition. The parat-lin wax had the following properties, as determined by the tests hereinabove designated: melting point :133 F., viscosity at 210 F.=37.9 SUS, oil content=0.4% by Weight, color=+27 Saybolt Universal, average molecular Weight=365, and refractive index at 212 F.=1.4196.
The microcrystalline wax was prepared by distilling The recovered Wax is the paraffin Wax employed slack Wax to remove the fractions boiling above about 525 F. Iat 2 mm. pressure. The residue `was dissolved in a solvent .at .a temperature of about 210 F. and the resulting solution chilled to a temperature of 50 F. The
precipitated -Wax was sepa-rated by liltration. The so-separated wax was again dissolved in solvent.v at an elevated due. The solvent remaining was theny removed from the wax by distillation. The recovered wax had the followi ing properties, using the tests above designated: melting point=193 F., viscosity at 210 F.=85 SUS, oil content=0.4%, average molecular weight=650, and refractive index at 212 F.=1.4363.`v
The oil component was prepared by distilling crude oi-l to recover Kabout 15 thereof yas residue. The residue was solvent-refined with propane yand phenol-cresol, and then devvaxed. The resulting heavy oil was distilled in the presence of clay to yield a heavy `residue which vwas the oil employed in the present composition and had the :following properties: A. P.l I. g-ravity=26.3, viscosity at 1lfm-:2634 SUS and at .210 F.=153.9 SUS, and viscosity index= 95. The initial boiling .point of the oil w-as about 766 F. and it contained about 127.5% aromatic hydrocarbons. n
Wax compositions having varying quantities of the parain wax, microcrystalline wax and oil, prepared as above described, were compounded and tested as follows: heavy paper stock employed for making cottage cheese containers was cut into strips of about 2 by `6 inches. The k strips were dipped finto the molten composition :of the 4in-Vl vention to form a desired weight of Wax per unit area of paper stock. 'I'he coated paper was then cooled to room temperature. Similar strips were coated with waxes heretofore used for coating such containers.
cated by passage of the dye solution through the Iwax bar- Y rier to the brous paper stock, which Was readily observable. Ihe quantities of the wax composition components, and results obtained, were as follows.
Micro Paratn Protec Bloei'- Sample crystalline Wax Oil Y tion 1 ing 2 lVax 30 70 pass. 20 80 pass. 30 65 pass. 15 80 fail. 30 64 pass.
1 Passage of dye solution through the wax coating, as above described,
does not pass the test, andis designated in the table as fa1l.
2 Compositions blocking at below 100"V F. were considered to fail the test; the compositions that passed the test had n. blocking temperature of atleast F. Y
the stated limits therefor, defeats the objects of ,they invention, a-s shown by the data.
. Example 2 Sample C of vExample 1 was duplicated except that the paraffin wax employed had a melting point of F. and an average molecular weight of 385. On testing the composition as described in Example 1, good protection was observed, i. e., a pass was obtained in the protection test, and a pass wasalso obtained in the blocking lest.
Example 3 A composition according to Example 2 was prepared except that aV different oilV was used. The oil boiled in A the lubricating oil range, had a viscosity at 100 F. of about 100 SUS and a viscosity index of about 95. Other properties were within the limitations as described above.
It was foundthat excellent results were obtained in both the protection and blocking tests as described for Example 1, a pass being obtained in both instances. The proportions of each of the three components to Cottage cheese containing bacteria known to deleteriously affect Wax.
employ are critical in 'the preparation of the composition of the invention. The quantity of parafn Wax to employ must be within the range of from 60-70% by weight, the quantity of microcrystalline wax to employ must be within the range of from 25-35% by Weight, and the quantity of oil to employ must be within the range of from 2-l0% by weight. The preferred composition, with which excellent results are obtained, contains 30% by weight of the microcrystalline wax, 65% by weight of the parain wax and 5% by weight of the oil. To emphasize the necessity of employing quantities of the wax composition components within the stated ranges, attention is now directed to the accompanying figure. The gure is a ternary diagram showing, by area ABCDEF, the permissible variations in the concentrations of the three components. If a composition dened by any point outside of area ABCDEF, be employed, the objects of the invention are defeated. For example, if a quantity of the microcrystalh'ne wax below the stated range is employed, the blocking temperature of the Wax coating becomes prohibitively low, whereas if quantities above the stated range are employed, the wax coating is not suiciently exible to provide adequate protection when coated on containers for packaging dairy products. For similar reasons the quantity of paraiin wax used must be within the stated range. The presence of the oil in a quantity within the defined range is necessary so that the wax coating has the proper ilexibility, but a quantity of oil above the stated limitation results in a composition that blocks at a temperature below about 100 F.
The invention claimed is:
1. A new composition of matter comprising: (A) from 60 to 70 parts of a paran wax having a melting point of from about 125 F. to 142 P., a viscosity of about 35 to 42 SUS at 210 F., a refractive index at 212 F. of from 1.419 to 1.423 and an average molecular Weight of from about 355 to about 400; (B) from 25 to 35 parts of a microcrystalline Wax boiling above about 525 F. at 2 mm. mercury pressure, and having a melting point of from about 185 F. to about 200 F., a viscosity at 210 F. of from about 8l to 89 SUS, a refractive index at 212 F. of from 1.435 to 1.438; and (C) from 2 to 10 parts of a lubricating oil having an API gravity of above 18 and an initial boiling point of above 600 F.
2. A new article of manufacture comprising a brous container for packaging dairy products coated with the composition of claim l.
3. Process for the preparation of a new composition of matter Which comprises admixing in the molten state: (A) from to 70 parts of a paran wax having a melting point of from about F. to 142 F., a viscosity of about 35 to 42 SUS at 210 F., a refractive index at 212 F. of from 1.419 to 1.423 and an average molecular weight of from about 355 to about 400; (B) from 25 to 35 parts of a microcrystalline wax boiling above about 525 F. at 2 mm. mercury pressure, and having a melting point of from about F. to about 200 F., a viscosity at 210 F. of from about 8l to 89 SUS, a refractive index at 212 F. of from 1.435 to 1.438; and (C) from 2 to l0 parts of a lubricating oil having an API gravity of above 18 and an initial boiling point of above 600 F., and solidifying the molten composition.
References Cited in the le of this patent UNITED STATES PATENTS 1,902,489 Clark Mar. 21, 1933 1,937,518 Henderson et al. Dec. 5, 1933 2,015,739 Winning Oct. 1, 1935 2,624,501 Ferris Ian. 6, 1953 2,668,140 Arabian Feb. 2, 1954 2,670,323 Hunter et Feb. 23, 19:54

Claims (1)

1. A NEW COMPOSITION OF MATTER COMPRISING: (A) FROM 60 TO 70 PARTS OF A PARAFFIN WAX HAVING A MELTING POINT OF FROM ABOUT 125* F. TO 142* F., A VISCOSITY OF ABOUT 35 TO 42 SUS AT 210* F., A REFRACTIVE INDEX AT 212* F. OF FROM 1.419 TO 1.423 AND AN AVERAGE MOLECULAR WEIGHT OF FROM ABOUT 355 TO ABOUT 400; (B) FROM 25 TO 35 PARTS OF A MICROCYSTALLINE WAX BOILING ABOVE ABOUT 525* F. AT 2 MM. MERCURY PRESSURE, AND HAVING A MELTING POINT OF FROM ABOUT 185* F. TO ABOUT 200* F., A VISCOSITY AT 210* F. OF FROM ABOUT 81 TO 89 SUS, A REFRACTIVE INDEX
US43054754 1954-05-18 1954-05-18 Wax composition Expired - Lifetime US2773812A (en)

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Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2842483A (en) * 1955-05-26 1958-07-08 British Petroleum Co Carton wax composition
US2885341A (en) * 1957-07-16 1959-05-05 Sun Oil Co Coating composition comprising paraffin wax, microcrystalline wax and petroleum distillate oil
US2937985A (en) * 1957-05-31 1960-05-24 Sun Oil Co Centrifugal separation of wax and oil
US2942766A (en) * 1959-02-27 1960-06-28 Sun Oil Co Wax coating compositions
US2943991A (en) * 1958-03-13 1960-07-05 Sun Oil Co Wax composition comprising a mixture of specific paraffin waxes and 1-2% of a microcrstalline wax
US2985538A (en) * 1959-09-24 1961-05-23 John W Padgett Wax coating composition and coated article
US3014002A (en) * 1959-09-03 1961-12-19 Atlantic Refining Co Wax coating and laminating composition and sheet material coated and laminated therewith
US3016312A (en) * 1958-07-02 1962-01-09 Sun Oil Co Wax coated cellophane
US3044917A (en) * 1960-01-19 1962-07-17 Sun Oil Co Wax composition
US3060045A (en) * 1959-11-17 1962-10-23 Socony Mobil Oil Co Inc Dairy container coating formulation
US3069346A (en) * 1959-01-20 1962-12-18 Sun Oil Co Wax composition
US3090538A (en) * 1961-06-27 1963-05-21 Sun Oil Co Wax composition having non-flaking characteristics for use in coating fibrous materials
US3128241A (en) * 1959-01-26 1964-04-07 Sinclair Research Inc Wax composition and method of producing same
US3155537A (en) * 1959-02-24 1964-11-03 Du Pont Rope finish
US3170864A (en) * 1961-06-27 1965-02-23 Exxon Research Engineering Co High quality dairy wax
US3379550A (en) * 1964-06-26 1968-04-23 Sinclair Research Inc Paraffin-microcrystalline wax composition
US3489600A (en) * 1966-02-08 1970-01-13 Celanese Corp Oxymethylene polymer-microcrystalline wax article
EP0141299A2 (en) * 1983-10-22 1985-05-15 H.B. Fuller GmbH Process for the coating of cheese

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1902489A (en) * 1931-08-24 1933-03-21 Gen Electric Insulating composition
US1937518A (en) * 1931-04-28 1933-12-05 Atlantic Refining Co Hydrocarbon wax
US2015739A (en) * 1935-10-01 Wax coating composition
US2624501A (en) * 1950-11-25 1953-01-06 Sun Oil Co Container having wax product coating
US2668140A (en) * 1950-05-24 1954-02-02 Shell Dev Preparation of paraffin waxes
US2670323A (en) * 1951-01-06 1954-02-23 California Research Corp Low melting paraffin wax

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2015739A (en) * 1935-10-01 Wax coating composition
US1937518A (en) * 1931-04-28 1933-12-05 Atlantic Refining Co Hydrocarbon wax
US1902489A (en) * 1931-08-24 1933-03-21 Gen Electric Insulating composition
US2668140A (en) * 1950-05-24 1954-02-02 Shell Dev Preparation of paraffin waxes
US2624501A (en) * 1950-11-25 1953-01-06 Sun Oil Co Container having wax product coating
US2670323A (en) * 1951-01-06 1954-02-23 California Research Corp Low melting paraffin wax

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2842483A (en) * 1955-05-26 1958-07-08 British Petroleum Co Carton wax composition
US2937985A (en) * 1957-05-31 1960-05-24 Sun Oil Co Centrifugal separation of wax and oil
US2885341A (en) * 1957-07-16 1959-05-05 Sun Oil Co Coating composition comprising paraffin wax, microcrystalline wax and petroleum distillate oil
US2943991A (en) * 1958-03-13 1960-07-05 Sun Oil Co Wax composition comprising a mixture of specific paraffin waxes and 1-2% of a microcrstalline wax
US3016312A (en) * 1958-07-02 1962-01-09 Sun Oil Co Wax coated cellophane
US3069346A (en) * 1959-01-20 1962-12-18 Sun Oil Co Wax composition
US3128241A (en) * 1959-01-26 1964-04-07 Sinclair Research Inc Wax composition and method of producing same
US3155537A (en) * 1959-02-24 1964-11-03 Du Pont Rope finish
US2942766A (en) * 1959-02-27 1960-06-28 Sun Oil Co Wax coating compositions
US3014002A (en) * 1959-09-03 1961-12-19 Atlantic Refining Co Wax coating and laminating composition and sheet material coated and laminated therewith
US2985538A (en) * 1959-09-24 1961-05-23 John W Padgett Wax coating composition and coated article
US3060045A (en) * 1959-11-17 1962-10-23 Socony Mobil Oil Co Inc Dairy container coating formulation
US3044917A (en) * 1960-01-19 1962-07-17 Sun Oil Co Wax composition
US3090538A (en) * 1961-06-27 1963-05-21 Sun Oil Co Wax composition having non-flaking characteristics for use in coating fibrous materials
US3170864A (en) * 1961-06-27 1965-02-23 Exxon Research Engineering Co High quality dairy wax
US3379550A (en) * 1964-06-26 1968-04-23 Sinclair Research Inc Paraffin-microcrystalline wax composition
US3489600A (en) * 1966-02-08 1970-01-13 Celanese Corp Oxymethylene polymer-microcrystalline wax article
EP0141299A2 (en) * 1983-10-22 1985-05-15 H.B. Fuller GmbH Process for the coating of cheese
EP0141299A3 (en) * 1983-10-22 1987-05-20 H.B. Fuller Gmbh Process for the coating of cheese

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