US2954337A

US2954337A - Composition of matter consisting of a microcrystalline wax and 5-25% of an aromatic petroleum extract

Info

Publication number: US2954337A
Application number: US368476A
Authority: US
Inventors: Edward J Martin
Original assignee: Sinclair Refining Co
Current assignee: Sinclair Refining Co
Priority date: 1953-07-16
Filing date: 1953-07-16
Publication date: 1960-09-27
Anticipated expiration: 1977-09-27

Description

Sept. 27, 1960 E. J. MARTIN 2,954,337 COMPOSITION OF MATTER CONSISTING OF A MICROCRYSTALLINE WAX AND 525% OF AN AROMATIC PETROLEUM EXTRACT Filed July 16, 1955 2 n z 53 c3 4 g: Z III M; m; m l Ol- 3g: m :3 2|: 3 u 3:: J u: a m 5/ u g; o

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N n -l N O u z l l I o o o o o o g m 8 0 0 e n l O 2 "NI/sup HLSNBULS Nouvmmn INVENTOR. Edward J. Martin ATTORNEYS r 2,954,337 Patented Sept. 27, 1960 COMPOSITION 'OF RTATTER CONSISTING 'OF A 4 Claims. (Cl. 208 -21) My invention relates to the production of novel microcrystalline wax compositions useful in .the lamination of materials.

Microcrystalline waxes are used to a great extent in v I the paper industry for'thelamination or bonding together of materials such as two or more sheets of glassine, cellophane, sulphite, kraft, and various metallicifoils'for the packaging of goods such as food and dairy products.

The wax serves asan adhesiveiand, .at the time time, acts,

as a barrier to the passage'of moisture, oil "and grease- =through the paper. 'larly suited for this purpose because of their properties Microcrystalline waxes are particuof tackiness, 'film flexibility, grease resistance, water and water vapor resistance, and adhesiveness. line waxes are the solid hydrocarbon mixtures that are separated from heavy petroleum distill-ates and residues .by conventional dewaxing processes. They :may .be deoiledto produce waxes ofcontrolledmeltingpoints and different degrees of hardness.

.I have found that deoilingamicrocrystalline wax frac -tion .to-a hardness correspondingto a needlefpenetration at 77 F. ofabout 2410 produces a waxofioptimum .laminationstrength. .I have .further found that .theaddi- .tion of aromaticpetroleum extracts to amicrocrystalline .a wax composition of increased lamination strength over that obtainable by deoiling the wax to its optimum strength. The flexibility of the wax composition is also improved. Thus, the wax compositions provide'.materials of greatly improved lamination strength for "the lamination or bonding together of various materials used for the packaging of various articles. 'In use, the wax compositions are applied to a material to be "laminated such as paperor foil' to'form a sheet orfilm and constitute a component part of .the material. They serve as an adhesive and as a barrier to the passage of moisture, oil

and grease when the material is used for-packaging.

By the term aromatic petroleum extracts, I mean the aromatic petroleum products obtained by conventional solvent extraction of petroleum oils, such as residual lubricating oil stocks, which are characterized 'bytheir tackiness, high aromaticity, high viscosity and flow viscosity index. The term includes aromatic extracts ob- 'tained from the solvent treating of residual lubricating oil stocks from Mid Continent and parafiin ibase cru'de's,

.for example with phenol, vfur'fural, nitrobenzene and the like, as well as the extracted aromatic residues known conventionally as petroleum resins which are the high molecular weight naturally contained viscous materials Microcryst'al-r 2 obtained by the solvent treating, for example, with propane, ofheavy residuallubricating oil fractions' from aMid-Continenb or na-phthenic base crude. Theseimaterials are readilyavailableiand relativelyinexpensive. By contrast, I have found that the addition to the ideoiled 'microcrystalline "wax fraction of jparafiinic petroleum materials such as .the corresponding .raifinate :from .the solvent treating of lubricating oil stocks, i.e. va solvent refined Mid-Continent lubricating .oil, .or high viscosity index petroleum resins from Pennsylvania crude do .not produce any improvement in lamination strength beyond that obtained by deoiling alone.

The compositions are prepared by first deoiling a microcrystalline wax fraction, e.g. petrolatum, toahardness corresponding to a needle penetration at 77 F. of less than about 24 to 25. For commercial operation, deoiling to a penetration of about 15 to 20 is satisfactory and additional expense need not be incurred by further deoiling. The base wax must be deoiled, however, to a penetration lower than the optimum penetration of about 24 to 25 before the aromatic petroleum extract is added in order to achieve the improved results. Addition of the extracttoa wax'which has not been deoiled to below this-penetration value does not improve the lamination strength-but on .the contrary *has an adverse elfect. An aromatic "petroleum extract is then added to the deoiled wax and the components are intimately admixed. The

' amoun'tof aromatic extract added may vary from about 1 to 2 5'percent based on the weight of the final composition. At least about 5 weight percent is required, however, to produce a composition of greater lamination strength than that obtainable by deoiling the base Wax. Amounts of about 5 to 20 weight percent are preferred as rthese give 'the'largest increase in lamination strength of .the compositions. .A proportion of about 10 to 12 percent produces an optimum laminating strength "at about the same penetration hardness corresponding .to the optimum lamination strength of the deoiled waxes. The improvement obtained'with thesearomatic materials appears to be independent of their viscosity. 7

The preparation and properties of the wax con1pos'i tions of my invention will be further illustrated byitlre following example and by reference -to Figure :l "which illustrates graphically the properties of thecomp'ositions.

Microcrystalline wax fractions of varying degrees o'f hardness were prepared *by deoiling a Mid-Continent petrolatum and the products tested 'for lamination strength, following which aromatic petroleum extracts were added to a deoiled wax "in varying proportions and -the products tested for lamination strength. i

in the example, the following testprocedure was used for measuring the lamination strength of -the compositions. 'Two sheets-of glassinepaper, "25 pounds'perream, were coated onone side with 4.5 to 5 .5 poundsper ream of the wax composition to be tested. The sheets-were trimmed and laminated by pressing them between two rolls. The bottom roll was heated to 210 F. with steam. The upper roll was a rubber roll weighted -s'o that'the bearing pressure between the rolls was 0175 'p'oun'd p'er inch. The laminated specimen was *aged under fixed conditions and then delarninated at a uniform 'rate using adelaminationtester. The amount of force in-grams=per inch to delaminate the test specimen was designated as "the'lamination strength. 7 v

The needle penetration was determined by D525 procedure modified in'thefollowing'manner. "The wax to be tested is completely melted "in an'oven and heated to 180 F. After-stirring it-is permitted to stand for fifteen minutes at 180 =F.-to allow any waterto separate. A one inch section cut from a's'tandard'two inch copper tube 'is used as a mold and is placed "on a sheet of aluminum foil on a stainless steel plate. The sampleis carefully poured into the mold, allowed to stand at 70 F.- 2 F. for one hour, and aged in a water bath at 77 F.:L 1 F. for two hours. It is then placed in a transfer dish of such capacity as to insure complete immersion of the wax mold and to maintain a temperature of 77 F..-l:l F. during the test. The needlepenetration is determined in accordance with ASTM D25 method using the 100 gram load and five seconds penetration with the test points selected on the cast surface as nearly as possible at one half the distance from the center of the sample to the side of the mold.

The physical properties of the deoiled microcrystalline wax fractions, including the Mid-Continent petrolatum, and the lamination strength test results are tabulated in Table I.

aniline point of 483 C., an iodine number of 63.8 and a molecular weight of 516519.

Another aromatic petroleum extract of the type known heavy residual lubricating oil stocks was also added in varying proportions to the 15 needle penetration deoiled as petroleum resin obtained by the solvent treating of wax and the resulting products tested for needle penetration and lamination strength. The aromatic resin had an API gravity of 9.9, a flash point of 540 F., a fire point of 625 F., a viscosity in SUS of 550,000 at 100 F., 1100 at 210 F., and 185.3 at 275 F., a viscosity index of 130, a pour point of 80 R, an OD. color of 1939, a carbon residue of 7.738, an ASTM ash of 0.027, an aniline point of 46.0 C., an iodine number of 83.0 and a molecular weight of 558.

The results are tabulated below in Table II.

Table II Wt. Percent Additive 1 Extract:

Penetration at 77 F. 15 16 17 18 19 24 31 39 48 R Lamination Strength, gins/in- 80 96 120 132 156,160 154 140 124 esm:

Penetration at 77 F. 15 16 17 18 23 31 36 42 Laminatlon Strength, glIlSJin 53. 3 90 98.6 120 130 160, 168 158 .152 144 1 Based on the final composition. 1 Modified ASTM D5-25 procedure.

Table I Microerystalline Base Waxes Petrolatum Penetration, at 77 F.

Gravity, API 35. 2 34. 5 34. 5 34. 1 33. 6 Viscosity, SUS/210 F 74.0 75. 9 77. 7 80. 8 77. 6 Petrolatum, M.P., F 160. 0 154. 5 155.0 158. 0 151. 5 Color, N PA 7-(dilute) 8 8 8 6- Percent Oil (D721-51T) 0.13 0. 01 0.19 0. 37 2. 72 Penetration, at 77 F.

(C) 33 Penetration, at 110 F.-- 46 Abrahams Hard, at

110 F 17.0 Lamination Strength,

gmsJin. 34 110 96 93 60 The results show that the optimum lamination strength of the waxes that can be obtained by a conventional solvent deoiling of petrolatum occurs at a needle penetration at 77 F. of 24. By reference to Figure 1, the curve resulting from the plotting of penetration against lamination strength of the deoiled waxes shows a gradual rise in lamination strength, as the wax is deoiled to a lower penetration value, to a peak optimum strength at a needle penetration at 77 F. of about 24 to 25, followed by a sharp decline.

If, however, aromatic extracts are added to the wax which has been deoiled to a hardness corresponding to a needle penetration at 77 F. of less than about 24 to 25 greatly improved lamination strength is obtained which is as much as about 50 percent more than the optimum lamination of the solvent deoiled waxes. For example, an aromatic petroleum extract obtained by the solvent treating of a lubricating oil stock was added in varying proportions to the 15 needle penetration deoiled wax of Table I and the resulting products tested for needle penetration and lamination strength. The aromatic extract oil had an API gravity of 11.5, a flash point of 510 R, a fire point of 595 F., a viscosity in SUS of 60,000 at 100 F., 9,604 at 130 F. and 405 at 210 F., a viscosity index of 72, a pour point of 55 R, an OD. Color of 943, a carbon residue of 4.176, ASTM ash of 0.003, an

The results show that the optimum lamination strength of the wax compositions containing aromatic extracts occurs at a needle penetration at 77 F. of about 24 as does the optimum strength of the deoiled microcrystalline waxes of Table I. The lamination strength of the wax compositions, however, is unexpectedly and greatly in creased at this needle penetration to as high as 168 grams per inch as compared to for the deoiled waxes. The surprising improvement is shown graphically in Figure 1 in which the curves resulting from the plotting of penetration against lamination strength of the wax compositions show a marked increase in lamination strength over the deoiled waxes at any penetration value and particularly at the penetration value corresponding to the optimum lamination strength of the deoiled waxes.

Thus, microcrystalline wax compositions of greatly improved lamination strength can be produced by the addition of readily available and relatively inexpensive materials to a deoiled microcrystalline wax thereby providing materials of improved utility in the lamination of materials such as paper and foils for the packaging of goods.

I claim:

1. A microcrystalline wax composition of improved lamination strength which essentially comprises a microcrystalline wax fraction base which has been deoiled to a hardness in terms of needle penetration at 77 F. of less than about 24 to 25 and about 5 to 25 weight percent based on the composition of an aromatic petroleum extract.

2. A microcrystalline wax composition of improved lamination strength which essentially comprises a microcrystalline wax fraction base which has been deoiled to a hardness in terms of needle penetration at 77 F. of about 15 to 20 and about 5 to 20 weight percent based on the composition of an aromatic petroleum extract.

3. The method of preparing a microcrystalline wax composition of improved lamination strength which comprises deoiling a microcrystalline wax fraction to a hardness corresponding to a needle penetration at 77 F. of less than about 24 to 25 and admixing therewith about 5 to 25 weight percent based on the composition of an aromatic petroleum extract.

5- 6 4. The method of preparing a microcrystalline waX 2,373,634 Wagner Apr. 10, 1945 composition of improved lamination strength which corn- 2,444,269 Phillips June 29, 1948 prises deoiling a microcrystalline wax fraction to a hard- 2,535,604 Schiermeyer Dec. 26, 1950 ness corresponding to a needle penetration at 77 F. of 2,598,257 Bennett et al. May 27, 1952 about 15 to 20 and admixing therewith about 5 to 20 5 2,599,130 Rumberger et a1 June 3, 1952 weight percent based on the composition of an aromatic 2,661,318 MacLaren et a1. Dec. 1, 1953 petroleum extract. 2,847,367 Walsh et a1 Aug. 12, 1958 References Cited in the file of this patent OTHER REFERENCES UNITED STATES PATENTS 10 Bennetts Commercial Waxes, Brooklyn, NY. 2,157,625 Page May 9, 1939 (1944), pages 60-62.

UNITED STATES PATENT OFFICE CERTIFICATE OF CORBECTIDN Patent N0, 2 954 337 September 27 l960-- Edward Ja Martin It is hereb$ certified that error appears in the-printed specification of the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.

Column 4 line 6 strike out "as petroleum resin obtained by the solvent treating of" and insert the same afterf'known" in line 3, same column 4; column 6, line 4,, list of references cited under "UNITED STATES PATENTS" for Bennett et al read Hill et a1 -B Signed and sealed this. 11th day of April 1961.

(SEAL) Attest:

ERNEST YY' THUR w. CROCKER Attesting- Ofiicer Acting Commissioner of Patents

Claims

1. A MICROCRYSTALLINE WAS COMPOSITION OF IMPROVED LAMINATION STRENGTH WHICH ESSENTIALLY COMPRISES A MICROCRYSTALLINE WAX FRACTION BASE WHICH HAS BEEN DEOILED TO A HARDNESS IN TERMS OF NEEDLE PENETRATION AT 77* F. OF LESS THAN ABOUT 24 TO 25 AND ABOUT 5 TO 25 WEIGHT PERCENT BASED ON THE COMPOSITION OF AN AROMATIC PETROLEUM EXTRACT.