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US4311181A Expired / Lapsed US ⏱️ 0.0 years remaining

Ambient temperature application of indicia to elastomer substrates

Assignee: Bridgestone Research LLC
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Filing: 1980-06-05
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Granted: 1982-01-19
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Expires: 2000-06-05
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Abstract

Abstract A process and composition for applying and bonding an indicia which is curable at ambient temperatures to a cured elastomer substrate. The substrate is treated generally at ambient temperatures with organic oxidants selected from the group consisting of N-halosulfonamides, N-halohydantoins, N-haloamides, N-haloimides, and the various isomers of mono-, di-, and trichloroisocyanuric acid. The indicia which is generally a urethane polymer or prepolymer is blended with an amine curing agent. A polar solvent is added to the amine curing agent and the amine curable polymer or prepolymer composition and mixed with the resulting blend or mixture applied to the treated elastomer surface in the form of an indicia so that said polymer or prepolymer cures at ambient temperature and is bonded to said elastomer. The invention is particularly suitable for applying indicia to various elastomer articles such as tires, conveyor belts, hoses, floor mats, sporting goods, and the like. An advantage of the invention is that the indicia can be made utilizing liquid components, mixed and applied at the site.

Inventors

  • 👤 Walter R. Hausch

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 22:05
CPC Classifications
B; B29; B29C; B29C65/00; B29C65/48; B29C65/4895; B29C66/00; B29C66/01; B29C66/05; B29C66/10; B29C66/11; B29C66/112; B29C66/1122; B29C66/40; B29C66/47; B29C66/472; B29C66/4724; B29C66/70; B29C66/71; B29C66/712; B29C73/00; B29C73/02; B29C73/16; B29C73/163; B29D; B29D30/00; B29D30/06; B29D30/52; B29D30/54; B29C66/02; B29C66/026; B29D30/72; B29D2030/728; B29K; B29K2021/00; B29L; B29L2023/00; B29L2023/005; B29L2030/00; B29L2031/00; B29L2031/709; B29L2031/7092; Y; Y10; Y10T; Y10T152/00; Y10T152/10; Y10T152/10495; Y10T428/00; Y10T428/13; Y10T428/1352; Y10T428/1386; Y10T428/24; Y10T428/24628; Y10T428/24736; Y10T428/24802; Y10T428/31504; Y10T428/31511; Y10T428/31551; Y10T428/31562; Y10T428/31569; Y10T428/31573; Y10T428/3158; Y10T428/31583; Y10T428/31587; Y10T428/31652; Y10T428/31663

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 229 words
An indicia residing on a substrate, comprising: a cured elastomer substrate; an amine cured prepolymer or polymer, said amine cured prepolymer or polymer cured at ambient temperature; a layer of a treating agent, said treating agent residing between said elastomer substrate and said amine cured prepolymer or polymer and forming a strong bond therebetween, said treating agent selected from the group consisting of the N-halohydantoins, the N-haloamides, and the N-haloimides; said amine cured prepolymer or polymer being in the form of an indicia; said substrate being an elastomer made from monomers selected from the group consisting of (a) dienes having from 4 to 12 carbon atoms, copolymers thereof, and interpolymers thereof, (b) natural rubber, (c) copolymers made from vinyl substituted aromatic compounds having from 8 to 15 carbon atoms and diene compounds having from 4 to 12 carbon atoms, (d) elastomers made from monomers of isobutylene and isoprene, (e) elastomers made from monomers of butadiene and acrylonitrile, (f) elastomers made from monomers of chloroprene, and (g) combinations thereof; and wherein said prepolymer or polymer is selected from the group consisting of (a) epoxy resins; (b) halogen-containing hydrocarbon polymers; (c) chlorosulfonated polymers; (d) polymers containing acid halide groups such as ##STR5## and haloformate groups such as ##STR6## (e) polymers containing anhydride groups which, on reaction with diamines, yield amide-acid linkages; (f) organopolysiloxanes; (g) urethane polymers or prepolymers; and combinations thereof.
Claim 2
Dependent Claim 229 words
An indicia residing on a substrate, comprising: a cured elastomer substrate; an amine cured prepolymer or polymer, said amine cured prepolymer or polymer cured at ambient temperature; a layer of a treating agent, said treating agent residing between said elastomer substrate and said amine cured prepolymer or polymer and forming a strong bond therebetween, said treating agent selected from the group consisting of the N-halohydantoins, the N-haloamides, and the N-haloimides; said amine cured prepolymer or polymer being in the form of an indicia; said substrate being an elastomer made from monomers selected from the group consisting of (a) dienes having from 4 to 12 carbon atoms, copolymers thereof, and interpolymers thereof, (b) natural rubber, (c) copolymers made from vinyl substituted aromatic compounds having from 8 to 15 carbon atoms and diene compounds having from 4 to 12 carbon atoms, (d) elastomers made from monomers of isobutylene and isoprene, (e) elastomers made from monomers of butadiene and acrylonitrile, (f) elastomers made from monomers of chloroprene, and (g) combinations thereof; and wherein said prepolymer or polymer is selected from the group consisting of (a) epoxy resins; (b) halogen-containing hydrocarbon polymers; (c) chlorosulfonated polymers; (d) polymers containing acid halide groups such as ##STR5## and haloformate groups such as ##STR6## (e) polymers containing anhydride groups which, on reaction with diamines, yield amide-acid linkages; (f) organopolysiloxanes; (g) urethane polymers or prepolymers; and combinations thereof.
Claim 3
Dependent Claim 18 words
An indicia according to claim 1, wherein said indicia extends along a limited portion of said elastomer substrate.
Claim 4
Dependent Claim 82 words
An indicia according to claim 2, wherein said elastomer substrate is cured and is selected from the group consisting of said elastomers made from said conjugated dienes, elastomers made from said conjugated dienes and said vinyl substituted aromatics, and said natural rubber; said elastomers made from said conjugated dienes being made from monomers selected from the group consisting of butadiene, isoprene, pentadiene, hexadiene, heptadiene, octadiene, 2,3-dimethylbutadiene, and 2,3-dimethyl-1,3-pentadiene; and wherein said amine cured polymer or prepolymer is said urethane polymer or prepolymer.
Claim 5
Dependent Claim 55 words
An indicia according to claim 3, wherein said elastomer substrate is selected from the group consisting of polybutadiene, natural rubber, and styrene-butadiene rubber, wherein said indicia is formed in a mold, and said mold is applied to said treated elastomer substrate so that said indicia adheres to said treated substrate when said mold is removed.
Claim 6
Dependent Claim 29 words
An indicia according to claim 4, wherein said treating agent is selected from the group consisting of 1,3-dichloro-5,5-dimethyl hydantoin; 1,3-dibromo-5,5-dimethyl hydantoin; 1,3-dichloro-5-methyl-5-isobutyl hydantoin; 1,3-dichloro-5-methyl-5-hexyl hydantoin; N-bromoacetamide; tetrachloroglycoluril; and N-bromosuccinimide.
Claim 7
Dependent Claim 26 words
An indicia according to claim 4, wherein said treating agent is selected from the group consisting of monochloroisocyanuric acid, dichloroisocyanuric acid, trichloroisocyanuric acid, and combinations thereof.
Claim 8
Dependent Claim 15 words
An indicia according to claims 1, or 6 wherein said elastomer substrate is a tire.
Claim 9
Dependent Claim 13 words
An indicia according to claim 7, wherein said tire is an off-the-road tire.
Claim 10
Dependent Claim 16 words
An indicia according to claim 1, or 7 wherein said elastomer substrate is a conveyor belt.
Claim 11
Dependent Claim 15 words
An indicia according to claims 1, or 7 wherein said elastomer substrate is a hose.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-01-18 1985-07-20 1986-01-19 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-01-18 1989-07-20 1990-01-19 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-01-18 1993-07-20 1994-01-19 $7700.00 Window Closed / Lapsed

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