US3142401A - Gasket composition - Google Patents

Gasket composition Download PDF

Info

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
Authority
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
Application number
US20638A
Inventor
George J Foss
Donald A Giessler
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Anchor Hocking Glass Corp
Original Assignee
Anchor Hocking Glass Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Anchor Hocking Glass Corp filed Critical Anchor Hocking Glass Corp
Priority to US20638A priority Critical patent/US3142401A/en
Application granted granted Critical
Publication of US3142401A publication Critical patent/US3142401A/en
Anticipated expiration legal-status Critical
Assigned to JPMORGAN CHASE BANK, AS COLLATERAL AGENT reassignment JPMORGAN CHASE BANK, AS COLLATERAL AGENT SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SEMICONDUCTOR COMPONENTS INDUSTRIES, LLC
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS 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
    • B65D41/00Caps, 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
    • B65D41/02Caps or cap-like covers without lines of weakness, tearing strips, tags, or like opening or removal devices
    • B65D41/04Threaded or like caps or cap-like covers secured by rotation
    • B65D41/0435Threaded or like caps or cap-like covers secured by rotation with separate sealing elements
    • B65D41/0442Collars or rings
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S260/00Chemistry of carbon compounds
    • Y10S260/37Closure

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.
US20638A 1960-04-07 1960-04-07 Gasket composition Expired - Lifetime US3142401A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (3)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US3142401A (en) Gasket composition
CN102123919B (en) Method of making a container closure
JP2660765B2 (en) Compression molded hermetic liner
US4256234A (en) Container closure having easily openable liner comprised of base resin, lubricant and 1 to 15% by weight of a conjugated diene resin
US4585135A (en) Screw closure
KR890001588B1 (en) Container lid with easy-open liner
EA029809B1 (en) Cap for a vessel for receiving foods or beverages
GB1563169A (en) Linerless closure
US3695477A (en) Plastisols and gaskets
EA026821B1 (en) Closure for a vessel for receiving foods or beverages
DE1066686B (en) Sealing compound based on a polyvinyl chloride resin for the production of a sealing ring
US11713166B2 (en) Low migration container
US20030176548A1 (en) Stiff and impact resistant compositions containing poly(propylene) or poly(ethylene/propylene) and calcium carbonate for closures
US3563402A (en) Plastic gasket rings and gasket linings
US3447710A (en) Manually removable tear-type closure elements
EP0478109A1 (en) Container closures and processes of making them
US3406854A (en) Gasket-forming plastisols comprising vinyl chloride resin, fatty acid amides and salt of lauryl sulfate
US3400094A (en) Gasket-forming compositions containing a mixture of unsaturated fatty acid amides as torque control agent
US3381837A (en) Gasket-forming compositions for container closures
US3933724A (en) Sealing compounds
US2880901A (en) Controlled torque gasket compositions
JPS58149268A (en) Closed cap
US3796681A (en) Low uniform removal torque gasket-forming plastisols
US3390800A (en) Controlled torque gasket compositions for container closure elements containing a mixture of mineral oil and fatty acid amides
US1425349A (en) Bottle closure

Legal Events

Date Code Title Description
AS Assignment

Owner name: JPMORGAN CHASE BANK, AS COLLATERAL AGENT, NEW YORK

Free format text: SECURITY INTEREST;ASSIGNOR:SEMICONDUCTOR COMPONENTS INDUSTRIES, LLC;REEL/FRAME:014830/0212

Effective date: 20030923