US4180166A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Patching kit with aggregate and two-part epoxy binder system
Assignee: Foster Products Corp
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Filing: 1978-11-13
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Granted: 1979-12-25
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Expires: 1998-11-13
Abstract
Abstract The disclosed method for applying an epoxy mortar is highly streamlined and involves little more than blending the curable epoxide binder for the mortar, adding aggregate and water to form the mortar, spreading the mortar on a surface, and curing the mortar in place on this surface. Flood coats, special trowelling techniques, and hydrophobic coatings for the aggregate particles are usually unnecessary. The simplification of the mortar-applying method depends upon formulating an epoxy binder material which includes a polyfunctional primary amine having an extremely low affinity for water, particularly a polynuclear cycloaliphatic polyamine such as methylene-bis-(4-cyclohexyl amine). A suitably formulated epoxy binder composition of this invention has a reasonably lengthy pot life, insensitivity to water, a relatively strong incompatibility with water (including the tendency to drive water out of a water/mortar emulsion so that the water forms a separate phase on the top surface of the mortar), good tensile and compressive strength after curing or hardening of the epoxy resin, a relatively low viscosity and easy spreadability during much of the pot life, and a high degree of lubricity with respect to metal trowels or other spreading tools.
Inventors
- 👤 Vernon H. Batdorf
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-27 21:59
CPC Classifications
C; C09; C09K; C09K3/00; C09K3/10; C04; C04B; C04B26/00; C04B26/02; C04B26/10; C04B26/14; C08; C08G; C08G59/00; C08G59/18; C08G59/40; C08G59/50; C08G59/5026; C04B2111/00; C04B2111/00474; C04B2111/00482; C09K2200/00; C09K2200/02; C09K2200/0243; C09K2200/0247; C09K2200/06; C09K2200/0645; C09K2200/0647
Claims Analysis
Total Claims: 15
Claim 1
Independent Claim
193 words
A method for coating a surface with an epoxide mortar comprising the steps of: (a) blending together the following substantially compatible components to form a curable epoxide binder material: 1. a substantially water insoluble curable vicinal epoxide composition including a polyglycidyl ether of a polyhydric phenol, said polyglycidyl ether having an epoxide functionality greater than 1 but less than about 3, 2. a substantially water insoluble polynuclear cycloaliphatic polyamine having a primary amine functionality greater than 1 but less than 4, 3. a hydrophobic agent, which agent includes a higher aliphatic group and a polar group; (b) adding at least 200 parts by weight of aggregate and a lubricating amount of water to each 100 parts by weight of said curable epoxide binder material, thereby forming a curable epoxide mortar containing a substantially incompatible water phase generally uniformly distributed through said epoxide mortar; (c) spreading a layer of said epoxide mortar onto a surface and permitting at least a portion of said substantially incompatible water phase to form a film of water on the top of said layer; and (d) curing said curable epoxide binder material in said layer to a thermoset solid.
Claim 2
Independent Claim
193 words
A method for coating a surface with an epoxide mortar comprising the steps of: (a) blending together the following substantially compatible components to form a curable epoxide binder material: 1. a substantially water insoluble curable vicinal epoxide composition including a polyglycidyl ether of a polyhydric phenol, said polyglycidyl ether having an epoxide functionality greater than 1 but less than about 3, 2. a substantially water insoluble polynuclear cycloaliphatic polyamine having a primary amine functionality greater than 1 but less than 4, 3. a hydrophobic agent, which agent includes a higher aliphatic group and a polar group; (b) adding at least 200 parts by weight of aggregate and a lubricating amount of water to each 100 parts by weight of said curable epoxide binder material, thereby forming a curable epoxide mortar containing a substantially incompatible water phase generally uniformly distributed through said epoxide mortar; (c) spreading a layer of said epoxide mortar onto a surface and permitting at least a portion of said substantially incompatible water phase to form a film of water on the top of said layer; and (d) curing said curable epoxide binder material in said layer to a thermoset solid.
Claim 3
Dependent Claim
12 words
A method according to claim 1 wherein said spreading step includes trowelling.
Claim 4
Dependent Claim
30 words
A method according to claim 2 wherein said curing of said curable epoxide binder occurs substantially spontaneously through interaction of said vicinal epoxide and said polyamine under normal ambient conditions.
Claim 5
Dependent Claim
29 words
A method according to claim 1 wherein said polynuclear cycloaliphatic polyamine is a non-fused ring, binuclear di(primaryamino) cycloalkane compound having a primary amine group on each non-fused cycloalkane ring.
Claim 6
Dependent Claim
17 words
A method according to claim 4 wherein each said non-fused cycloalkane ring is a six-member carbocyclic ring.
Claim 7
Dependent Claim
59 words
A method according to claim 5 wherein said hydrophobic agent is selected from the group consisting of: (a) a metal salt of a higher alkanoic acid; (b) a higher alkyl phenoxy poly(oxyethylene) ethanol surfactant; and (c) an amine of the formula R--NH--A--NH 2 , wherein R represents an open-chain, higher aliphatic radical and A is a lower alkylene radical.
Claim 8
Dependent Claim
57 words
A method according to claim 1 wherein said epoxide binder material has a Brookfield viscosity less than 12,000 c.p.s. and comprises: (a) a diglycidyl ether of bisphenol A having an epoxide equivalent weight ranging from about 160 to about 1,000; (b) a bis (primary aminocyclohexyl) methane; (c) an N-higher alkyl-1,3-propane diamine; and (d) a silane adhesion promoter.
Claim 9
Dependent Claim
25 words
A method according to claim 1 wherein said lubricating amount of water is at least 5% by weight, based on the weight of said aggregate.
Claim 10
Dependent Claim
135 words
A two-part curable epoxy binder system for use in binding together an aggregate having a Brookfield viscosity less than 3,000 centipoise when initially blended and before curing, said system comprising: in a first part having a Brookfield viscosity less than 3,000 centipoise, a substantially water insoluble curable vicinal epoxide composition comprising a polyglycidyl ether of a polyhydric phenol having an average epoxide functionality greater than 1 but less than 3 and an amine-reactive, viscosity reducing diluent therefor, for reducing the viscosity to below 3,000 centipoise; in an active hydrogen, epoxide-reactive second part capable of curing said first part, (a) a substantially water-insoluble, non-fused ring, di-primaryamino-bi-cycloalkane and (b) a substantially water insoluble N-higher aliphatic alkyl-1,3-propane diamine, the ratio of amino equivalents of said compound (a) to said compound (b) ranging from about 0.5:1 to about 2:1.
Claim 11
Dependent Claim
135 words
A two-part curable epoxy binder system for use in binding together an aggregate having a Brookfield viscosity less than 3,000 centipoise when initially blended and before curing, said system comprising: in a first part having a Brookfield viscosity less than 3,000 centipoise, a substantially water insoluble curable vicinal epoxide composition comprising a polyglycidyl ether of a polyhydric phenol having an average epoxide functionality greater than 1 but less than 3 and an amine-reactive, viscosity reducing diluent therefor, for reducing the viscosity to below 3,000 centipoise; in an active hydrogen, epoxide-reactive second part capable of curing said first part, (a) a substantially water-insoluble, non-fused ring, di-primaryamino-bi-cycloalkane and (b) a substantially water insoluble N-higher aliphatic alkyl-1,3-propane diamine, the ratio of amino equivalents of said compound (a) to said compound (b) ranging from about 0.5:1 to about 2:1.
Claim 12
Dependent Claim
35 words
A two-part curable composition according to claim 9 wherein said polyglycidyl ether of a polyhydric phenol is a polyglycidyl ether of bisphenol A having an epoxide equivalent weight ranging from about 170 to about 200.
Claim 13
Dependent Claim
14 words
A two-part curable composition according to claim 9 wherein said di-primaryamino-bi-cycloalkane is bis(4-aminocyclohexyl) methane.
Claim 14
Dependent Claim
79 words
A patching kit for aggregate-filled, cured epoxide coatings comprising the two-part epoxy binder system of claim 9, and, packaged with said two-part epoxy binder system but in a container separate from said two-part epoxy binder system: a mortar-forming amount of aggregate, said amount being at least 200 parts by weight per 100 parts by weight of said two-part epoxy binder system, and a lubricating amount of water, said lubricating amount being at least 5% by weight of said aggregate.
Claim 15
Dependent Claim
25 words
A patching kit according to claim 12 wherein said lubricating amount of water is preblended with said aggregate to provide water-moistened aggregate in said container.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1982-12-24 | 1983-06-25 | 1983-12-25 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1986-12-24 | 1987-06-25 | 1987-12-25 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1990-12-24 | 1991-06-25 | 1991-12-25 | $7700.00 | Window Closed / Lapsed |