US3142401A - Gasket composition - Google Patents
Gasket composition Download PDFInfo
- Publication number
- US3142401A US3142401A US20638A US2063860A US3142401A US 3142401 A US3142401 A US 3142401A US 20638 A US20638 A US 20638A US 2063860 A US2063860 A US 2063860A US 3142401 A US3142401 A US 3142401A
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- US
- United States
- Prior art keywords
- closure
- gasket
- plastisol
- container
- composition
- 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
Links
- 239000000203 mixture Substances 0.000 title claims description 29
- 229920001944 Plastisol Polymers 0.000 claims description 23
- 239000004999 plastisol Substances 0.000 claims description 23
- 238000007789 sealing Methods 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000004014 plasticizer Substances 0.000 claims description 10
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims description 2
- 229920003023 plastic Polymers 0.000 claims description 2
- 239000004033 plastic Substances 0.000 claims description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 20
- 150000001408 amides Chemical class 0.000 description 13
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 9
- 229940037312 stearamide Drugs 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 8
- SFIHQZFZMWZOJV-HZJYTTRNSA-N linoleamide Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(N)=O SFIHQZFZMWZOJV-HZJYTTRNSA-N 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 6
- SFIHQZFZMWZOJV-UHFFFAOYSA-N Linolsaeure-amid Natural products CCCCCC=CCC=CCCCCCCCC(N)=O SFIHQZFZMWZOJV-UHFFFAOYSA-N 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920006385 Geon Polymers 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- 229910001864 baryta Inorganic materials 0.000 description 2
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 229940126543 compound 14 Drugs 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- TUTWLYPCGCUWQI-UHFFFAOYSA-N decanamide Chemical compound CCCCCCCCCC(N)=O TUTWLYPCGCUWQI-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000010437 gem Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940081141 hexadecanamide Drugs 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229940116335 lauramide Drugs 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- QEALYLRSRQDCRA-UHFFFAOYSA-N myristamide Chemical compound CCCCCCCCCCCCCC(N)=O QEALYLRSRQDCRA-UHFFFAOYSA-N 0.000 description 1
- LTHCSWBWNVGEFE-UHFFFAOYSA-N octanamide Chemical compound CCCCCCCC(N)=O LTHCSWBWNVGEFE-UHFFFAOYSA-N 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000001038 titanium pigment Substances 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D41/00—Caps, e.g. crown caps or crown seals, i.e. members having parts arranged for engagement with the external periphery of a neck or wall defining a pouring opening or discharge aperture; Protective cap-like covers for closure members, e.g. decorative covers of metal foil or paper
- B65D41/02—Caps or cap-like covers without lines of weakness, tearing strips, tags, or like opening or removal devices
- B65D41/04—Threaded or like caps or cap-like covers secured by rotation
- B65D41/0435—Threaded or like caps or cap-like covers secured by rotation with separate sealing elements
- B65D41/0442—Collars or rings
-
- 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
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/37—Closure
Definitions
- This invention relates to compounds which may be added to gasket lining compositions of the plastisol type, for the purpose of bringing within controllable limits the opening and closing torques of closures in sealing and unsealing containers.
- An object of this invention is therefore to provide an additive which may be inserted in plastisol forming compositions for closure gaskets so as to reduce the coefficient of friction between the plastisol and a glass container and to bring the opening torque within desirable limits, regardless of the fact that the sealed container may have been stored for long periods of time and that it may have been subjected to considerable changes of temperature due to weather or other factors.
- Another object of this invention is to provide a plastisol gasket additive which is not harmful to the human body, will not contaminate foods or have any objectionable odor.
- Still another object of this invention is to provide a plastisol gasket additive which may easily be mixed with other plastisol forming ingredients and flowed with them into metal closure caps without the necessity of heating the composition before or during the owing-in operation.
- compositions of the same general types may be used with the invention, such as organosols and formulations including vinyl polymer or copolymer resins which are generally fluXed with a plasticizer to produce a rubber-like composition.
- the essence of the present invention lies in the discovery that acid amides used as additives in plastisol gasket compositions produce a torque control which varies only slightly as a result of changes in temperature and as Patented July 28, 1964 a result of the passage of time from the time of sealing until the closure is removed. This new and improved result is highly desirable. It has been discovered that acid amides, when added to a plastisol formulation, will mix easily with it and provide a composition which may be flowed into metal caps without any previous heating.
- Armids are products manufactured by the Armour Chemical Division of Armour and Co., in Chicago, Illinois. These consist of acid amides, singly or in mixtures, such acid amides being generally derived from various fatty acids.
- Armid-O is a composition containing 91% oleamide (9-octadecanamide), 6% stearamide (octadecanamide), 3% linoleamide, (9,12-octadecadienamide) by weight.
- a basic formula, Formula #1, in accompanying Table I was discovered to be particularly satisfactory. Experiments were continued, varying the proportions of Armids employed and at times also adding new compounds. The results obtained with the basic formula and variations thereof are given below:
- Geon 120X3, 121 and 202 are resins which are solvated by the plasticizer at elevated temperatures thus forming an elastic and rubbery permanent gel upon cooling. These materials are manufactured by the B. F. Goodrich Chemical Co. Baryta White is a liller which lessens the material cost of the plastisol and functions synergistically with the lubricant or lubricants employed.
- GP-261 is a plasticizer which solvates the resins at elevated temperatures and also gives fluidity to the unfused plastisol.
- Paraplex G-62 is also a plasticizer and functions as does GP-261, but it is used in these formulas primarily as a stabilizer against high temperature discoloration.
- Titanox 16S-LO is a product ofthe Titanium Pigment Corp., a white pigment to add color to the plastisol.
- Acrawax C, glycerin, parathn and flexible wax were utilized with the acid amides in several of the formulations as illustrated in the accompanying tables. As Formula 13 in Table III indicates, Acrawax C was found to give particularly desirable results when used in conjunction with Ohopex Q-10. When utilized with GP- 261, however, these various additives were not always helpful, as Table II, shows in Formulas 7, 8 and 9. Acrawax C is a hard synthetic wax manufactured by Glyco Products Company.
- Armid-O is mostly composed of oleamide (91%), with small amounts of linoleamide and stearamide added (3% and 6%, respectively).
- Armid HT mostly consists of stearamide (75%) with 22% of palmitamide (hexadecanamide) and 3% oleamide also entering the composition.
- Armid C is a composition consisting of 49% lauramide (dodecanamide), 17% myristamide (tetradecanamide), 9% palrnitamide, 8% caprylamide (octanamide), 7% capramide (decanarnide), 6% oleamide, and 2% each of stearamide and linoleamide.
- Armid 18 is a composition made up almost entirely of stearamide (93%) with 5% palmitamide, and 2% oleamide added.
- Armowax is the Armour Chemical Divisions tradename for methylene bis-stearamide.
- the preparation of the composition described in Formula #l is typical of the others and is accomplished as follows: all of the ingredients are blended together except for one third of the plasticizer, until the resins are thoroughly dispersed. The remaining one third of the plasticizer is then added and also thoroughly dispersed. To' facilitate the incorporation of the acid amide additive in the plastisol, it is melted in the plasticizer. The mixture is then cooled to at least 90 F. prior to the blending in of other ingredients, With the exception of melting the acid amide additive, all operations of compound mixing and lining of caps, are performed at room temperature (SW-90 F.). Thus the temperature of the plastisol composition need at no time be raised above room temperature except for cold winter days when it may be necessary to raise the plastisol temperature to F. This temperature rise may be facilitated by agitation.
- FIG. 1 is a side elevational view partially in section of a typical closure cap for use with the gasket conipounds of the invention
- FIG. 2 is a bottom plan view of the closure cap of FIG. 1;
- FIG. 3 is a sectional view of the closure cap taken along lines 3-3 of FIG. 2;
- FIG. 4 is a sectional view corresponding to FIG. 3 showing the closure cap applied to a container with the closure gasket compound in sealing engagement with the rim of the container.
- the gasket compounds of this invention having acid amide lubricants to control the slippage of gaskets on sealing surfaces, are suitable for the various types of closures utilizing gaskets, including threaded caps, interrupted thread caps, and lug-type caps.
- FIGS. 1 through 4 the gasket compound is applied to a well known lug-type closure 1 to form a sealing gasket 2 therein.
- This typical closure l has a metal shell with a cover 3 and a depending skirt 4 having container engaging lugs 5 formed at its lower edge.
- An annular channel 6 is provided adjacent the periphery of the cover 3 to receive the gasket compound which may be owed into the channel 6 or otherwise applied.
- the lugs 5 are threaded into engagement with cooperating threads or lugs 8 on the container 7 and the gasket 2 is drawn into sealing engagement with the container linish 9 as illustrated in FIG. 4.
- the gasket compounds of the invention with the acid amide lubricants tix the removal torque within predetermined limits as the closure 1 is removed from the container 7 by controlling the friction forces between the closure finish 9 and the contacting surface of the gasket 2.
- the acid amides are included in suiiicient amounts as illustrated in the formula tables so that the friction reducing effects of the lubricants are obtained on the surface of the gasket 2 which is in contact with the closure finish 9.
- gasket forming compositions are produced which, because of the use of acid amides as torque controlling agents, are eminently satisfactory for use in closures for both bottles and jars, and because of the extreme simplicity of their application as well as the excellent results obtained, represent an advance over the prior art in comparable gasket formulations.
- the acid amide additives will bloom to the surface of the plastisol composition, and thereby provide the lubrication necessary so as to obtain the torque control required by the objects of the present invention.
- a container sealing closure to be applied and removed by rotation of the closure about an axis perpendicular to the plane of the -opening of the container, carrying on its inner surface a gasket comprising a thin layer of a sealing composition comprising a plastic matrix of a vinyl polymer and an amount of a plasticizer therefor suicient to form a plastisol and including a minor proportion of a torque control agent uniformly distributed therein, said torque control agent including at least one long chain aliphatic carboxylic acid amide.
- torque control agent is predominantly lauramide, in admixture with minor amounts of myristamide, palmitamide, caprylamide, capramide, oleamide, stearamide, and linoleamide.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Closures For Containers (AREA)
Description
Juy 28, 1964 G. J. Foss ETAL 3,142,401
GASKET COMPOSITION Filed April 7. 1960 IN VEN TORS Gems d. Foss BY Dor/44o Grasse: YMWJ United States Patent O 3,142,451 GASKET COMPSlTlON George J. Foss and Donald A. Giessler, Lancaster, Ohio,
assigner-s to Anchor Hocking Glass Corporation, Lancaster, Ghia, a corporation of Delaware Filed Apr. 7, 126i), Ser. No. 20,638 6 Claims. (Cl. 21S-45) This invention relates to compounds which may be added to gasket lining compositions of the plastisol type, for the purpose of bringing within controllable limits the opening and closing torques of closures in sealing and unsealing containers.
The use of vinyl chloride resins, especially the so-called plastisol formulations, as gasket material to line the inside of metal closures, has developed rapidly in recent years. Such plastisol gaskets are satisfactory in many respects, and they present certain advantages over other well-known types of gaskets. Considerable difficulty, however, has resulted from the fact that the elasticity of plastisols varies substantially with changes in temperature and with the passage of time. A closure cap applied originally to a container with a proper removal torque value may become tightly frozen after it is stored so as to be diflicult to remove by hand. On the other hand, a change in temperature may render the cap so loose as to expose its contents to loss, spoilage or contamination before they reach the consumer. Generally, it has been found that for each size of closure, there is a maximum opening torque which permits easy removal of the cap by the user, but attempts to keep the opening torques always below the desirable limits have frequently failed in the past.
An object of this invention is therefore to provide an additive which may be inserted in plastisol forming compositions for closure gaskets so as to reduce the coefficient of friction between the plastisol and a glass container and to bring the opening torque within desirable limits, regardless of the fact that the sealed container may have been stored for long periods of time and that it may have been subjected to considerable changes of temperature due to weather or other factors.
Another object of this invention is to provide a plastisol gasket additive which is not harmful to the human body, will not contaminate foods or have any objectionable odor.
Still another object of this invention is to provide a plastisol gasket additive which may easily be mixed with other plastisol forming ingredients and flowed with them into metal closure caps without the necessity of heating the composition before or during the owing-in operation.
Other and further objects of the invention will be obvious upon an understanding of the illustrative embodiment about to be described or will be indicated in the appended claims, and Various advantages not referred to herein will occur to one skilled in the art upon employment of the invention in practice.
Although the specifications herein generally refer to plastisols, it is understood that other compositions of the same general types may be used with the invention, such as organosols and formulations including vinyl polymer or copolymer resins which are generally fluXed with a plasticizer to produce a rubber-like composition.
The use of lubricants in various types of gaskets for controlling the torque in sealing and removal of screw closures is known in the art and has been used commercially as described in Patent No. 1,899,821 to Parker.
The essence of the present invention lies in the discovery that acid amides used as additives in plastisol gasket compositions produce a torque control which varies only slightly as a result of changes in temperature and as Patented July 28, 1964 a result of the passage of time from the time of sealing until the closure is removed. This new and improved result is highly desirable. It has been discovered that acid amides, when added to a plastisol formulation, will mix easily with it and provide a composition which may be flowed into metal caps without any previous heating.
After subsequent iluxing of the composition inside the cap, a satisfactory gasket results and the closure, when applied to a glass container, does not require an excessive opening torque even though subjected to unusually low temperatures such as are met under refrigerating conditions prior to removal of the closures. The tests conducted with Armid-O, a material the composition of which is given below, were particularly successful in these respects, as it was found that the low opening torques with closures containing that compound were not adversely affected by either unusually high or low storage temperatures or by prolonged storage periods prior to opening of the container.
In practising the invention, use was made especially of various Armids, which are products manufactured by the Armour Chemical Division of Armour and Co., in Chicago, Illinois. These consist of acid amides, singly or in mixtures, such acid amides being generally derived from various fatty acids. For instance Armid-O is a composition containing 91% oleamide (9-octadecanamide), 6% stearamide (octadecanamide), 3% linoleamide, (9,12-octadecadienamide) by weight. A basic formula, Formula # 1, in accompanying Table I, was discovered to be particularly satisfactory. Experiments were continued, varying the proportions of Armids employed and at times also adding new compounds. The results obtained with the basic formula and variations thereof are given below:
TABLE I Plastisol Formulas and Removal Torques Geen 120X3 60 60 60' 60 Geon 202 40 40 40 40 Baryta. White 50 100 -26 75 80 70 70 Paraplex G62 5 5 6 5 Titanox 16B-LO 5 5 5 5 Armd 0 4 5 3 3 Aerawax C 3 Removal Torques (in inch lbs.):
Hot Pack-82 mln.-
Average 40. 2 44. 2 41. 65. 0 nge 29-48 34-65 37-49 49-86 Hot Pack-63 mm Average. 27. 2 Range 24-34 TABLE II Plastzsol Formulas and Removal Torques Geon 121 60 60 60 60 60 Goon 202 40 40 4() 40 40 Baryta White- 50 50 50 50 50 GP-261- 75 75 75 75 Para-plex G-62 5 5 5 5 5 Titanox lG8-LO 5 5 5 5 5 Armitl O 4 6 4 4 4 Glycern 1 Parallm 2 Flexible War 2 Removal Turques (in inch lbs):
Hot Rick-82 mm.-
Average 43. 3 43. 8 47. 2 47.0 48. 5 Range 41-46 41-49 45-49 43-52 43-54 Hot Pack-63 nlm.-
Average 31. 5 31. 8 35. 7 31. 7 33. 3 Range 27-35 26-36 29-50 27-43 26-40 TABLE III F ormzllas and Removal Torques [O1eamide, stearamide, and various acid amides] Plnstisol Compound 14 Armownx. Removal Torques:
63 mm. Twist Caps- Average. 57. 2 37. 8 46. 8 44. 8
Range 34-75 33-44 44-50 42-48 70 mm. Twist Caps- Average 62. 2 60. 8
Range 52-75 51-68 In the above tables, Geon 120X3, 121 and 202 are resins which are solvated by the plasticizer at elevated temperatures thus forming an elastic and rubbery permanent gel upon cooling. These materials are manufactured by the B. F. Goodrich Chemical Co. Baryta White is a liller which lessens the material cost of the plastisol and functions synergistically with the lubricant or lubricants employed. GP-261 is a plasticizer which solvates the resins at elevated temperatures and also gives fluidity to the unfused plastisol. Paraplex G-62 is also a plasticizer and functions as does GP-261, but it is used in these formulas primarily as a stabilizer against high temperature discoloration. It is a product of the Rohm & Haas Co. Ohopex Q-10, a product of Ohio Apex, Inc., is a plasticizer made up of a mixture of fatty, phthalic acid esters. Titanox 16S-LO is a product ofthe Titanium Pigment Corp., a white pigment to add color to the plastisol.
Acrawax C, glycerin, parathn and flexible wax were utilized with the acid amides in several of the formulations as illustrated in the accompanying tables. As Formula 13 in Table III indicates, Acrawax C was found to give particularly desirable results when used in conjunction with Ohopex Q-10. When utilized with GP- 261, however, these various additives were not always helpful, as Table II, shows in Formulas 7, 8 and 9. Acrawax C is a hard synthetic wax manufactured by Glyco Products Company.
As has been pointed out already above, Armid-O is mostly composed of oleamide (91%), with small amounts of linoleamide and stearamide added (3% and 6%, respectively).
Armid HT mostly consists of stearamide (75%) with 22% of palmitamide (hexadecanamide) and 3% oleamide also entering the composition.
Armid C is a composition consisting of 49% lauramide (dodecanamide), 17% myristamide (tetradecanamide), 9% palrnitamide, 8% caprylamide (octanamide), 7% capramide (decanarnide), 6% oleamide, and 2% each of stearamide and linoleamide.
Armid 18 is a composition made up almost entirely of stearamide (93%) with 5% palmitamide, and 2% oleamide added.
Armowax is the Armour Chemical Divisions tradename for methylene bis-stearamide.
The preparation of the composition described in Formula #l is typical of the others and is accomplished as follows: all of the ingredients are blended together except for one third of the plasticizer, until the resins are thoroughly dispersed. The remaining one third of the plasticizer is then added and also thoroughly dispersed. To' facilitate the incorporation of the acid amide additive in the plastisol, it is melted in the plasticizer. The mixture is then cooled to at least 90 F. prior to the blending in of other ingredients, With the exception of melting the acid amide additive, all operations of compound mixing and lining of caps, are performed at room temperature (SW-90 F.). Thus the temperature of the plastisol composition need at no time be raised above room temperature except for cold winter days when it may be necessary to raise the plastisol temperature to F. This temperature rise may be facilitated by agitation.
A typical closure cap for use with the gasket compounds of the invention has been chosen for purposes of illustration and description and is shown in the accompanying drawings forming a part of the specification, wherein:
FIG. 1 is a side elevational view partially in section of a typical closure cap for use with the gasket conipounds of the invention;
FIG. 2 is a bottom plan view of the closure cap of FIG. 1;
FIG. 3 is a sectional view of the closure cap taken along lines 3-3 of FIG. 2; and
FIG. 4 is a sectional view corresponding to FIG. 3 showing the closure cap applied to a container with the closure gasket compound in sealing engagement with the rim of the container.
The gasket compounds of this invention, having acid amide lubricants to control the slippage of gaskets on sealing surfaces, are suitable for the various types of closures utilizing gaskets, including threaded caps, interrupted thread caps, and lug-type caps. In FIGS. 1 through 4 the gasket compound is applied to a well known lug-type closure 1 to form a sealing gasket 2 therein. This typical closure l has a metal shell with a cover 3 and a depending skirt 4 having container engaging lugs 5 formed at its lower edge. An annular channel 6 is provided adjacent the periphery of the cover 3 to receive the gasket compound which may be owed into the channel 6 or otherwise applied. When the closure 1 is applied to the container 7, the lugs 5 are threaded into engagement with cooperating threads or lugs 8 on the container 7 and the gasket 2 is drawn into sealing engagement with the container linish 9 as illustrated in FIG. 4. The gasket compounds of the invention with the acid amide lubricants tix the removal torque within predetermined limits as the closure 1 is removed from the container 7 by controlling the friction forces between the closure finish 9 and the contacting surface of the gasket 2. The acid amides are included in suiiicient amounts as illustrated in the formula tables so that the friction reducing effects of the lubricants are obtained on the surface of the gasket 2 which is in contact with the closure finish 9.
It will be seen that by the present invention as expressed in the formulas in the foregoing charts, gasket forming compositions are produced which, because of the use of acid amides as torque controlling agents, are eminently satisfactory for use in closures for both bottles and jars, and because of the extreme simplicity of their application as well as the excellent results obtained, represent an advance over the prior art in comparable gasket formulations. In effect, the acid amide additives will bloom to the surface of the plastisol composition, and thereby provide the lubrication necessary so as to obtain the torque control required by the objects of the present invention.
As various changes may be made in the form, construction, and arrangement of the parts herein without departing from the spirit and scope of the invention, and without sacrificing any of its advantages, it is to be understood that all matter herein is to be interpreted as i1lustrative and not in a limiting sense.
Having thus described our invention, we claim:
1. A container sealing closure to be applied and removed by rotation of the closure about an axis perpendicular to the plane of the -opening of the container, carrying on its inner surface a gasket comprising a thin layer of a sealing composition comprising a plastic matrix of a vinyl polymer and an amount of a plasticizer therefor suicient to form a plastisol and including a minor proportion of a torque control agent uniformly distributed therein, said torque control agent including at least one long chain aliphatic carboxylic acid amide.
2. The closure of claim 1, in which the amount of the torque control agent is between about 1.6% and about 2.5% by Weight of the plastisol.
3. The closure of claim 1, in which the torque control agent is predominantly oleamide, in adrniXture with minor amounts of stearamide and linoleamide.
4. The closure of claim 1, in which the torque control agent is predominantly stearamide, in admixture with minor amounts of palmitamide and oleamide.
5. The closure of claim 1, in which the torque control agent is predominantly lauramide, in admixture with minor amounts of myristamide, palmitamide, caprylamide, capramide, oleamide, stearamide, and linoleamide.
6. The closure of claim 1, in which the torque control agent consists essentially of about 91% oleamide, 6% stearamide, and about 3% linoleamide, by Weight.
References Cited in the le of this patent UNITED STATES PATENTS OTHER REFERENCES 26 Chem. & Eng. News, page 2205, advertisement, July 26, 1948.
Claims (1)
1. A CONTAINER SEALING CLOSURE TO BE APPLIED AND REMOVED BY ROTATION OF THE CLOSURE ABOUT AN AXIS PERPENDICULAR TO THE PLANE OF THE OPENING OF THE CONTAINER, CARRYING ON ITS INNER SURFACE A GASKET COMPRISING A THIN LAYER OF A SEALING COMPOSITION COMPRISING A PLASTIC MATRIX OF A VINYL POLYMER AND AN AMOUNT OF A PLASTICIZER THEREFOR SUFFICIENT TO FORM A PLASTISOL AND INCLUDING A MINOR PROPORTION OF A TORQUE CONTROL AGENT UNIFORMLY DISTRIBUTED THEREIN, SAID TORQUE CONTROL AGENT INCLUDING AT LEAST ONE LONG CHAIN ALIPHATIC CARBOXYLIC ACID AMIDE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20638A US3142401A (en) | 1960-04-07 | 1960-04-07 | Gasket composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20638A US3142401A (en) | 1960-04-07 | 1960-04-07 | Gasket composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3142401A true US3142401A (en) | 1964-07-28 |
Family
ID=21799742
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US20638A Expired - Lifetime US3142401A (en) | 1960-04-07 | 1960-04-07 | Gasket composition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3142401A (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3231529A (en) * | 1960-11-18 | 1966-01-25 | Grace W R & Co | Gasket compositions comprising polyvinyl chloride and vinyl ester interpolymers |
| US3286868A (en) * | 1965-10-06 | 1966-11-22 | Owens Illinois Inc | Container and closure for same |
| US3365089A (en) * | 1966-11-29 | 1968-01-23 | Grace W R & Co | Gasket-forming compositions for container closures |
| US3365090A (en) * | 1966-11-29 | 1968-01-23 | Grace W R & Co | Gasket-forming compositions for container closures |
| US3371057A (en) * | 1965-09-27 | 1968-02-27 | Sinclair Research Inc | Coating composition of improved "slip" characteristics |
| US3371811A (en) * | 1964-11-20 | 1968-03-05 | Corning Glass Works | Container closure |
| US3381837A (en) * | 1966-11-29 | 1968-05-07 | Grace W R & Co | Gasket-forming compositions for container closures |
| US3390800A (en) * | 1965-12-22 | 1968-07-02 | Grace W R & Co | Controlled torque gasket compositions for container closure elements containing a mixture of mineral oil and fatty acid amides |
| US3400094A (en) * | 1965-12-22 | 1968-09-03 | Grace W R & Co | Gasket-forming compositions containing a mixture of unsaturated fatty acid amides as torque control agent |
| US3406854A (en) * | 1965-12-22 | 1968-10-22 | Grace W R & Co | Gasket-forming plastisols comprising vinyl chloride resin, fatty acid amides and salt of lauryl sulfate |
| US3448881A (en) * | 1967-05-02 | 1969-06-10 | Continental Can Co | Closure with means to control opening torque |
| US3563402A (en) * | 1968-02-09 | 1971-02-16 | Heinrich Arnold | Plastic gasket rings and gasket linings |
| US4209176A (en) * | 1979-01-11 | 1980-06-24 | Baxter Travenol Laboratories, Inc. | Nose seal assembly |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2464855A (en) * | 1944-10-26 | 1949-03-22 | Bakelite Corp | Vinyl resin composition containing a stearic acid amide of ethylene diamine |
| GB810786A (en) * | 1955-11-29 | 1959-03-25 | Crown Cork & Seal Co | Improved container closure and material therefor |
| US2880901A (en) * | 1956-04-27 | 1959-04-07 | White Cap Co | Controlled torque gasket compositions |
-
1960
- 1960-04-07 US US20638A patent/US3142401A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2464855A (en) * | 1944-10-26 | 1949-03-22 | Bakelite Corp | Vinyl resin composition containing a stearic acid amide of ethylene diamine |
| GB810786A (en) * | 1955-11-29 | 1959-03-25 | Crown Cork & Seal Co | Improved container closure and material therefor |
| US2880901A (en) * | 1956-04-27 | 1959-04-07 | White Cap Co | Controlled torque gasket compositions |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3231529A (en) * | 1960-11-18 | 1966-01-25 | Grace W R & Co | Gasket compositions comprising polyvinyl chloride and vinyl ester interpolymers |
| US3371811A (en) * | 1964-11-20 | 1968-03-05 | Corning Glass Works | Container closure |
| US3371057A (en) * | 1965-09-27 | 1968-02-27 | Sinclair Research Inc | Coating composition of improved "slip" characteristics |
| US3286868A (en) * | 1965-10-06 | 1966-11-22 | Owens Illinois Inc | Container and closure for same |
| US3390800A (en) * | 1965-12-22 | 1968-07-02 | Grace W R & Co | Controlled torque gasket compositions for container closure elements containing a mixture of mineral oil and fatty acid amides |
| US3406854A (en) * | 1965-12-22 | 1968-10-22 | Grace W R & Co | Gasket-forming plastisols comprising vinyl chloride resin, fatty acid amides and salt of lauryl sulfate |
| US3400094A (en) * | 1965-12-22 | 1968-09-03 | Grace W R & Co | Gasket-forming compositions containing a mixture of unsaturated fatty acid amides as torque control agent |
| US3365090A (en) * | 1966-11-29 | 1968-01-23 | Grace W R & Co | Gasket-forming compositions for container closures |
| US3381837A (en) * | 1966-11-29 | 1968-05-07 | Grace W R & Co | Gasket-forming compositions for container closures |
| US3365089A (en) * | 1966-11-29 | 1968-01-23 | Grace W R & Co | Gasket-forming compositions for container closures |
| US3448881A (en) * | 1967-05-02 | 1969-06-10 | Continental Can Co | Closure with means to control opening torque |
| US3563402A (en) * | 1968-02-09 | 1971-02-16 | Heinrich Arnold | Plastic gasket rings and gasket linings |
| US4209176A (en) * | 1979-01-11 | 1980-06-24 | Baxter Travenol Laboratories, Inc. | Nose seal assembly |
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