US20070264527A1 - System and method for increasing the bond strength between a structural material and its reinforcement - Google Patents

System and method for increasing the bond strength between a structural material and its reinforcement Download PDF

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US20070264527A1
US20070264527A1 US11/234,184 US23418405A US2007264527A1 US 20070264527 A1 US20070264527 A1 US 20070264527A1 US 23418405 A US23418405 A US 23418405A US 2007264527 A1 US2007264527 A1 US 2007264527A1
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Prior art keywords
reinforcing material
matrix
frit
coating
selecting
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US11/234,184
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Melvin Sykes
Charles Weiss
Donna Day
Philip Malone
Earl Baugher
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US Department of Army
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US Department of Army
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Priority to US11/234,184 priority Critical patent/US20070264527A1/en
Assigned to ARMY, UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY reassignment ARMY, UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BAUGHER, JR., EARL H., DAY, DONNA C., MALONE, PHILIP G., SYKES, MELVIN C., WEISS, JR., CHARLES A.
Priority to PCT/US2006/037501 priority patent/WO2007038518A2/en
Publication of US20070264527A1 publication Critical patent/US20070264527A1/en
Priority to US12/793,799 priority patent/US20100247860A1/en
Priority to US13/178,067 priority patent/US8859105B2/en
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C26/00—Coating not provided for in groups C23C2/00 - C23C24/00
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/38—Fibrous materials; Whiskers
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/38—Fibrous materials; Whiskers
    • C04B14/48—Metal
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
    • C04B20/0048—Fibrous materials
    • C04B20/0068—Composite fibres, e.g. fibres with a core and sheath of different material
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/16—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
    • C04B35/18—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay rich in aluminium oxide
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/71—Ceramic products containing macroscopic reinforcing agents
    • C04B35/74—Ceramic products containing macroscopic reinforcing agents containing shaped metallic materials
    • C04B35/76—Fibres, filaments, whiskers, platelets, or the like
    • E—FIXED CONSTRUCTIONS
    • E04—BUILDING
    • E04C—STRUCTURAL ELEMENTS; BUILDING MATERIALS
    • E04C5/00—Reinforcing elements, e.g. for concrete; Auxiliary elements therefor
    • E04C5/01—Reinforcing elements of metal, e.g. with non-structural coatings
    • E04C5/015—Anti-corrosion coatings or treating compositions, e.g. containing waterglass or based on another metal
    • E—FIXED CONSTRUCTIONS
    • E04—BUILDING
    • E04C—STRUCTURAL ELEMENTS; BUILDING MATERIALS
    • E04C5/00—Reinforcing elements, e.g. for concrete; Auxiliary elements therefor
    • E04C5/01—Reinforcing elements of metal, e.g. with non-structural coatings
    • E04C5/015—Anti-corrosion coatings or treating compositions, e.g. containing waterglass or based on another metal
    • E04C5/017—Anti-corrosion coatings or treating compositions containing cement
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C14/00—Glass compositions containing a non-glass component, e.g. compositions containing fibres, filaments, whiskers, platelets, or the like, dispersed in a glass matrix
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/14—Glass frit mixtures having non-frit additions, e.g. opacifiers, colorants, mill-additions

Definitions

  • Nickel and cobalt-rich glass frits bond to steel and the glass frits on the steel bond to bulk construction materials embedded in the glass frits on the steel.
  • These bulk materials may comprise portland cement clinker, mica, quartz, aluminum silicate, other refractory inorganic compounds, and the like. These bulk materials are bound in the surface of the glass frits, in turn bonding tightly to the calcium silicate hydrate that forms as the portland cement in the concrete hydrates.
  • FIG. 1 depicts an element that may be used in an embodiment of the present invention.
  • FIG. 2 is a photograph of a metal rod treated in accordance with an embodiment of the present invention.
  • FIG. 3 is a photograph of a fractured split section of a portland cement-based mortar cylinder and the rod of FIG. 2 after it has been extracted a short distance from the cylinder.
  • FIG. 4 is a photograph of the split section of the mortar cylinder of FIG. 3 after the rod has been removed from the mortar cylinder.
  • steel rods are coated with a coating (glaze) incorporating a commercial powdered glass frit and particles of one or more refractory materials such as mica, glass slag, portland cement clinkers and the like.
  • the frit and refractory material are suspended in a liquid carrier, such as water.
  • Refractory materials are those materials that do not melt at temperatures that fuse (solidify) frits used in making the coatings (glazes) used in select embodiments of the present invention.
  • coatings or glazes (“enameling”) of a rough finish texture are fired on metal structure.
  • the resultant “rough-enamel” coating is employed to improve the bonding of a variety of cement-based mortars or concretes to a variety of metals, such as steel, stainless steel, aluminum, copper and the like, or items plated with these metals.
  • flowable frit mixtures preferably in a liquid carrier mixed with a thickener added to the liquid, are mixed with a refractory additive of appropriate dimension to yield a rough or “bumpy” enameled surface after firing.
  • the refractory additives may be one or more of the following types: dry portland cement, mica, slag, and the like. These refractory additives are mixed with one or more suitable frits and applied as one or more coatings (glazes) on reinforcing materials such as steel rebar, metal fibers, and the like.
  • a reinforcement coated with one or more of the above “frit-bonding” mixtures (or rough glazes) appropriately fired on the reinforcing material, e.g., rebar is added as reinforcement to structural material during its flowable stage (such stage as may be present in a portland cement-based mortar paste or concrete paste) and then permitted to cure.
  • the selected frit in the mixture needs to bond to steel.
  • the frit contains a transition metal, e.g., nickel, cobalt, and the like, to facilitate this bond. Bonding of the “coated (glazed) and fired” steel to an embedding matrix, such as concrete in its paste form, is most likely not improved by applying multiple coats of a “frit-bonding” mixture.
  • a suitable bonding frit for steel is a groundcoat enamel that bonds directly to the steel, not to another enamel.
  • the coating is produced by mixing into (suspending in) the groundcoat enamel one or more high melting point (refractory) materials, such as a ceramic of portland cement clinkers, mica flakes, slag glass and the like.
  • refractory high melting point
  • a method for improving a bond between reinforcing material and a matrix incorporating the reinforcing material comprises: selecting one or more flowable frits, such as an alkali-resistant groundcoat enamel, the frits compatible with the matrix and reinforcing material; selecting refractory material compatible with the matrix, reinforcing material and frits; mixing the refractory material with the frits to yield one or more coatings (glazes); preparing one or more surfaces of the reinforcing material; applying one or more coatings (glazes) to the surfaces; selecting a temperature regime for firing the coatings (glazes) onto the reinforcing material; selecting a time regime for conducting the firing; firing the coatings (glazes) on the reinforcing material at the selected temperature regime for the selected time regime; cooling the resultant coated (glazed) reinforcing material; inserting the resultant cooled reinforcing material into the matrix while the matrix is flowable, and curing the resultant reinforced flowable matrix
  • a method for reinforcing a matrix by incorporating an enhanced reinforcing material therein comprises: selecting one or more flowable frits compatible with the matrix and the reinforcing material; selecting refractory material compatible with the matrix, the reinforcing material and the frits; mixing the refractory material with the frits to yield one or more coatings (glazes); preparing one or more surfaces of the reinforcing material; applying one or more of the coatings (glazes) to the surfaces; selecting a temperature regime for firing the coatings (glazes) onto the reinforcing material; selecting a time regime for conducting the firing; firing the coatings (glazes) on the reinforcing material at the selected temperature and time regimes; cooling the resultant coated (glazed) reinforcing material; inserting the resultant cooled coated (glazed) reinforcing material into the matrix while the matrix is flowable, and curing the resultant reinforced flowable matrix.
  • a method for producing an enhanced reinforcing material for incorporating in a matrix comprises: selecting one or more flowable frits compatible with the matrix and a base reinforcing material; selecting refractory material compatible with the matrix, the base reinforcing material and the frits; mixing the refractory material with the frits to yield one or more coatings (glazes); preparing one or more surfaces of the base reinforcing material; applying one or more of the coatings (glazes) to one or more of the surfaces; selecting a temperature regime for firing the coatings (glazes) onto the reinforcing material; selecting a time regime for conducting the firing; firing the coatings (glazes) on the reinforcing material at the selected temperature and time regimes and cooling the resultant coated (glazed) reinforcing material.
  • a configuration is affixed to a base reinforcing material for improving the bond between the base reinforcing material and an initially flowable matrix incorporating the enhanced reinforcing material.
  • the configuration comprises one or more flowable frits compatible with the matrix and the base reinforcing material and refractory material compatible with the matrix, the base reinforcing material and the frits, such that: the refractory material is mixed with the frits to yield one or more coatings (glazes); one or more surfaces of the reinforcing material are prepared for accepting the coatings (glazes); one or more coatings (glazes) are applied to the prepared surfaces, the coatings (glazes) are fired on the reinforcing material during a pre-specified temperature regime and for a pre-specified time regime; the resultant coated (glazed) reinforcing material is cooled; the resultant cooled enhanced reinforcing material is inserted into the matrix while the matrix is flowable and the resultant reinforced flowable matrix is
  • an enhanced reinforcing structure for improving bonding of the enhanced reinforcing structure to a matrix incorporating the enhanced reinforcing structure comprises: one or more base reinforcing materials, each having one or more surfaces suitable for coating; one or more flowable frits compatible with the matrix and the base reinforcing materials and refractory material compatible with the matrix, the base material and the frits, such that: the refractory material is mixed with the frits to yield one or more coatings (glazes); one or more surfaces of the base material are prepared for accepting the coatings (glazes); one or more coatings (glazes) are applied to one or more of the prepared surfaces; one or more of the coatings (glazes) are fired onto one or more of the surfaces during a pre-specified temperature regime over a pre-specified time regime; the resultant enhanced reinforcing structure is cooled; the resultant cooled enhanced reinforcing structure is inserted into the matrix while the matrix is flowable and the resultant flowable matrix
  • surfaces of the base reinforcing material are prepared for coating by cleaning and degreasing.
  • the base reinforcing material is selected from the group consisting of: metal fibers, metal rods, steel fibers, steel rods, metal alloy fibers, metal alloy rods, metal, metal alloys, steel, stainless steel, aluminum, copper, material plated with metal, and combinations thereof.
  • steels that may be used are selected from the group consisting of: low-carbon steel; decarburized steel; interstitial-free steel, i.e., steels in which carbon and nitrogen are contained in an alloying element such as titanium, niobium, vanadium and the like; titanium-stabilized steel, and combinations thereof.
  • the initially flowable matrix is a cement-based paste selected from the group consisting of: portland cement-based mortars; portland cement-based concretes; phosphate-cement based mortars; phosphate-cement based concretes; aluminum silicate cement-based mortars; aluminum silicate cement-based concretes, and combinations thereof.
  • frits are selected from the group consisting of: a ground glass, a ground glass slag, a frit suspended in a liquid, a glass frit suspended in a liquid, a powdered frit, a powdered glass frit, a frit containing transition metals, a frit containing cobalt, a frit containing nickel, an alkali-resistant glass frit, and combinations thereof.
  • coatings comprise approximately equal amounts by volume of a frit and a refractory material.
  • the frit may be a powdered glass frit and the refractory material dry portland cement, such as a type I-II portland cement.
  • the dry portland cement may be provided in a proportion of up to about 70% by volume of the final mix.
  • the coating (glaze) may comprise a frit suspended in a liquid and a dry refractory material in approximately equal amounts by volume of the liquid suspension and the refractory material.
  • the coating may comprise equal amounts by volume of a liquid suspension of an alkali-resistant glass frit and dry portland cement, such as a type I-II portland cement.
  • the liquid suspension of an alkali-resistant glass frit may be a commercially available enamel groundcoat.
  • the steps are:
  • steel parts treated with this process After drying at 93-150° C., steel parts treated with this process have a light straw color.
  • low-carbon decarburized steel is enameled in a direct operation, the steel is etched to remove 11-22 g/m 2 of surface metal and receives a surface deposit of 0.9-1.3 g/m 2 of nickel.
  • a ferric sulfate etching solution is sometimes used with decarburized steel.
  • coatings are applied via a method selected from the group consisting of: spraying, dipping, brushing, flowing on, electrostatic spraying, rolling, and combinations thereof.
  • the temperature regime involves inserting the coated (glazed) reinforcing material into an oven pre-heated to the final temperature of said firing.
  • the final temperature of firing the coating (glaze) is from about 500° C. to about 900° C., and preferably from about 800° C. to about 875° C.
  • the time regime is that time after inserting the coated (glazed) reinforcing material into an oven pre-heated to the final temperature of firing until removal of the fired reinforcing material from the oven.
  • the time of firing is selected to be from about two minutes to about 45 minutes and preferably from about 15 minutes to about 30 minutes.
  • cooling of the fired reinforcing material is done by removing the fired reinforcing material from the oven and permitting the reinforcing material to reach ambient temperature in ambient air.
  • portland cement is employed as both the refractory material to be mixed with a frit and at least part of the composition of the matrix to be reinforced.
  • Portland cement-based concrete begins as a strong alkaline paste. This paste varies in pH from about the pH of calcium hydroxide (12.5) to almost 14 depending on the amount of sodium present. This high alkalinity dictates selection of a frit that is alkali-resistant.
  • alkali-resistant glass is made by adding zirconium to the basic silica-sodium-borate composition.
  • a highly alkaline paste attacks glass, it typically forms a gel that tends to swell unless the gel is stabilized with a lithium compound.
  • frits are selected from among existing (commercial) alkali-resistant frits. Some examples include “Cermet” from Thompson Enamel Co., Bellevue, Ky.; “Frit 2680 Transparent,” also from Thompson; and “F-579 Frit” from Fusion Ceramics, Inc., Carrollton, Ohio.
  • one or more flowable frits are mixed with one or more refractory materials (i.e., those inorganic materials having a melting point higher than that of the frits) such as portland cement clinkers, mica flakes, and the like.
  • the resultant mixture is compatible with an embedding matrix, such as a portland cement-based mortar, in which the enhanced reinforcing material is to be inserted.
  • the “frit-bonding” coating may eliminate or reduce the rate of corrosion of metal or metal-plated reinforcement coated with it in accordance with an embodiment of the present invention.
  • the embedding matrix such as a portland cement-based concrete or mortar paste
  • the embedding matrix may be designed to etch, and thus bond with a particular established glass coating (enamel) on a reinforcement, such as rebar.
  • the glass (enamel) coating on the reinforcement material may be abraded to form a rough (more chemically active) surface and a dry “powdered” refractory material, such as portland cement or glass slag and the like, applied to the roughened surface to enhance the bond of the reinforcement to a structural matrix, such as portland cement-based mortar or concrete.
  • flowable frit materials may be mixed with a refractory material to yield a coating mixture (glaze) that is subsequently applied to the surface of a base reinforcement material and fired.
  • the resultant coated (glazed) reinforcement material is permitted to cool and then inserted in an initially flowable matrix, such as a paste of a portland cement-based mortar or concrete.
  • equal volumes of a ground glass frit, preferably an alkali-resistant frit, and portland cement are mixed to prepare a mixture to be used as a “bonding-frit” coating (glaze).
  • the glass may be a mixture of glass types such as are available from a recycling plant. More than 50% by volume portland cement may be used. In select embodiments of the present invention, up to about 70% by volume of the bonding-frit coating (glaze) may be portland cement.
  • the texture of the resultant bonding-frit coating (glaze) mixture may range from a fine sand, such as a quartz sand, to a fine powder, such as portland cement.
  • a “ground glass” bonding-frit coating is applied by making a slurry of the mixture of ground glass and portland cement using water or water mixed with a thickener or adhesive, such as methyl cellulose.
  • the base reinforcing item such as a steel rebar, may be coated by dipping, spraying, brushing, rolling or flow coating the slurry onto the surface.
  • the resultant wet coating is typically air-dried prior to firing.
  • the bonding-frit coating mixture may be applied in its dry state by electro-static spray such as any of the methods used in commercial powder coating.
  • the method may be used to strongly bond two pieces of material each incorporating a rough (bumpy) enameled surface, prepared in accordance with embodiments of the present invention, at the interface to be joined.
  • the two pieces may be joined by applying a suitable matrix, such as a portland cement-based grout, as an adhesive.
  • a method of enhancing bonding between surfaces of materials comprises: selecting one or more first and one or more second surfaces to be bonded; selecting one or more first flowable frits compatible with materials comprising the first surfaces; selecting first refractory material compatible with the first surfaces and the first frits; mixing the first refractory material with the first frits to yield one or more first coatings; preparing the first surfaces; applying one or more first coatings to the first surfaces; selecting one or more second flowable frits compatible with the materials comprising the second surfaces; selecting second refractory material compatible with the second surfaces and the second frits; mixing the second refractory material with the second frits to yield one or more second coatings; preparing the second surfaces; applying the second coatings to the second surfaces; selecting one or more temperature regimes for firing each of the first and second coatings onto the first and second surfaces, respectively; selecting a time regime for conducting each of the firings of the first and second coatings; firing the first and second coatings onto the first and second surfaces
  • the bonding-frit coating was prepared by mixing about 50% by volume of a portland cement type I-II with a 50% by volume of a commercial alkali-resistant ground coat enamel to yield a frit-bonding liquid coating.
  • this coating was applied to the experimental rods and fired at temperatures from about 805-870° C. At this temperature range, heat exposure ranged from about 2-12 minutes.
  • the goal was to produce a final coating (glaze) that is about 50-100 ⁇ m (2-4 mils) thick, including the refractory material embedded therein. Thin spots were corrected by applying more bonding-frit coating (glaze) at the thin areas and firing a second time.
  • the surfaces of experimental steel rods “enhanced” in accordance with an embodiment of the present invention were prepared by: cleaning with an alkali-based solution; water rinsing preferably with warm water (in a range of about 45-60° C.); water rinsing, preferably with cold water (ambient, i.e., about 15-25° C.); acid-etching in a sulfuric acid solution of about 6-8%; cold rinsing with a dilute sulfuric acid solution of pH of about 3.0-3.5; nickel deposition at about 0.02 to 0.06 g/m 2 as described above from Porcelain Enameling ; cold rinsing in a dilute sulfuric acid solution of pH about 3.0-3.5; and final rinsing in a sodium carbonate/sodium borate solution.
  • FIG. 2 depicting a photograph of one of the coated (glazed) and fired experimental rods 20 . None of the experimental rods 20 were abraded.
  • the experimental rods were dipped into a water-based suspension of commercial glass frit (VitrearcTransparent Prussian Blue Cat. No. 2680, Thompson-Enamel Co., Bellevue, Ky.), portland cement (PC) type I-II, and methyl cellulose thickener (Klyr-Fire #A-1, Thompson-Enamel Co., Bellevue, Ky.).
  • the experimental rods 20 were permitted to air-dry and then fired in an electric furnace, resulting in a finished product 20 as represented in FIG.
  • the rods 10 , 20 were inserted to a depth of 65 mm in a 76 mm (3 in) diameter, 152 mm (6 in) long cylinder containing a portland cement-based mortar paste.
  • the standard mortar described in the ASTM C 109 section on proportioning was used to prepare the mortar cylinders. After the rods 10 , 20 were inserted in the mortar paste; each cylinder was consolidated by vibrating the mortar paste for thirty seconds. All cylinders were moist-cured for seven days.
  • FIG. 3 a photograph of a section 31 of a typical cylinder split lengthwise along one side of the inserted rod 30 .
  • the rod 30 has been extracted in the direction of the arrow 34 only a short distance as indicated at the arrow 32 to show a small portion of the void 33 resultant from extraction.
  • FIG. 3 also shows how the experimental rod 30 was stripped completely of its coating (glaze) 22 .
  • FIG. 4 a view of the mortar section 31 of FIG. 3 with the rod 30 removed completely.
  • the darkened area is the entire void 33 showing the fired glaze 22 remaining attached within the mortar matrix 31 after the experimental rod 30 was pulled out, i.e., the bond of the fired frit-bonding coating (glaze) 22 to the mortar section 31 was stronger than the bond of the coating (glaze) 22 to the steel rod 30 .
  • the adhesion between the mortar and the rods 10 , 20 was determined by measuring the peak load required to pull the rods free from the mortar such that peak load equaled break load. The results of the testing are presented in Table 3. The load required for pull-out was measured by using an MTS Material Testing System (Minneapolis, Minn.).
  • Results for the control rods 10 were similar to those obtained with earlier tests with similar uncoated rods.
  • the greatest adhesion between the experimental rods 20 and the mortar 31 was noted with the experimental rods 20 that were treated with a coating (glaze) containing a frit-bonding mixture of a glass frit and portland cement, i.e., a coating (glaze), that was fired on the rod 20 .
  • a coating i.e., a coating (glaze)
  • Coating with the “frit-bonding” coating mixture (glaze) of a portland cement type I-II and glass frit and firing the resultant coating (glaze) produced adhesion that was nearly three times greater than that measured for the control rods 10 .
  • the frit-bonding coating (glaze) incorporating a commercial glass frit and portland cement performs better than the fusing of portland cement to an established enamel or abrading enamel and fusing portland cement thereto, the latter two described above as approaches one and two, respectively.
  • a nail and a screw may not be structural equivalents in that a nail employs a cylindrical surface to secure wooden parts together, whereas a screw employs a helical surface, in the environment of fastening wooden parts, a nail and a screw may be equivalent structures.

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Abstract

A method of coating a reinforcing material, such as a metal, increases the adhesion between the material and a matrix, such as a cement-based mortar or concrete, in which the material is embedded. In one embodiment, a glass frit mixed with a refractory material, such as dry portland cement, is bonded, typically by heat, to the surface of the material. The reaction of the refractory component when the metal is embedded in fresh mortar or concrete prevents the formation of soft precipitates at the interface of the matrix and its reinforcement. One embodiment involves mixing portland cement Type I-II with a glass frit as a coating, coating a steel reinforcing rod and firing the coating to bond to the metal. The frit-refractory coating produces a strong bond between the metal reinforcement and its concrete or mortar matrix and may eliminate or significantly reduce the potential for corrosion of the reinforcement.

Description

    STATEMENT OF GOVERNMENT INTEREST
  • Under paragraph 1(a) of Executive Order 10096, the conditions under which this invention was made entitle the Government of the United States, as represented by the Secretary of the Army, to an undivided interest therein on any patent granted thereon by the United States. This and related patents are available for licensing to qualified licensees. Please contact Phillip Stewart at 601 634-4113.
    • BACKGROUND
  • Metals embedded in concrete typically form very poor bonds with the contacting cement because there are no coupling compounds that form between the cement and the metal. In select embodiments of the present invention, nickel and cobalt-rich glass frits bond to steel and the glass frits on the steel bond to bulk construction materials embedded in the glass frits on the steel. These bulk materials may comprise portland cement clinker, mica, quartz, aluminum silicate, other refractory inorganic compounds, and the like. These bulk materials are bound in the surface of the glass frits, in turn bonding tightly to the calcium silicate hydrate that forms as the portland cement in the concrete hydrates.
    • BRIEF DESCRIPTION OF DRAWINGS
  • FIG. 1 depicts an element that may be used in an embodiment of the present invention.
  • FIG. 2 is a photograph of a metal rod treated in accordance with an embodiment of the present invention.
  • FIG. 3 is a photograph of a fractured split section of a portland cement-based mortar cylinder and the rod of FIG. 2 after it has been extracted a short distance from the cylinder.
  • FIG. 4 is a photograph of the split section of the mortar cylinder of FIG. 3 after the rod has been removed from the mortar cylinder.
    • DETAILED DESCRIPTION
  • Adding material of a non-melting mineral type, i.e., refractory material, to a low-melting temperature glass frit; mixing the two as a coating (glaze); coating some reinforcing steel rods with the resultant mix and firing the resultant coating (glaze) increases the strength of the bond to concrete as compared to uncoated (unglazed) steel rods, such as rebar used to reinforce concrete. In select embodiments of the present invention, steel rods are coated with a coating (glaze) incorporating a commercial powdered glass frit and particles of one or more refractory materials such as mica, glass slag, portland cement clinkers and the like. In select embodiments of the present invention, the frit and refractory material are suspended in a liquid carrier, such as water. Refractory materials are those materials that do not melt at temperatures that fuse (solidify) frits used in making the coatings (glazes) used in select embodiments of the present invention.
  • In select embodiments of the present invention, coatings or glazes (“enameling”) of a rough finish texture are fired on metal structure. The resultant “rough-enamel” coating is employed to improve the bonding of a variety of cement-based mortars or concretes to a variety of metals, such as steel, stainless steel, aluminum, copper and the like, or items plated with these metals.
  • In select embodiments of the present invention, flowable frit mixtures, preferably in a liquid carrier mixed with a thickener added to the liquid, are mixed with a refractory additive of appropriate dimension to yield a rough or “bumpy” enameled surface after firing. In select embodiments of the present invention, the refractory additives may be one or more of the following types: dry portland cement, mica, slag, and the like. These refractory additives are mixed with one or more suitable frits and applied as one or more coatings (glazes) on reinforcing materials such as steel rebar, metal fibers, and the like. In select embodiments of the present invention, a reinforcement coated with one or more of the above “frit-bonding” mixtures (or rough glazes) appropriately fired on the reinforcing material, e.g., rebar, is added as reinforcement to structural material during its flowable stage (such stage as may be present in a portland cement-based mortar paste or concrete paste) and then permitted to cure.
  • In select embodiments of the present invention, the selected frit in the mixture (coating or glaze) needs to bond to steel. Thus, the frit contains a transition metal, e.g., nickel, cobalt, and the like, to facilitate this bond. Bonding of the “coated (glazed) and fired” steel to an embedding matrix, such as concrete in its paste form, is most likely not improved by applying multiple coats of a “frit-bonding” mixture. Thus, with steel rebar for example, it is proper to use a mixture of a suitable bonding frit and a refractory material. A suitable bonding frit for steel is a groundcoat enamel that bonds directly to the steel, not to another enamel. In select embodiments of the present invention, the coating (glaze) is produced by mixing into (suspending in) the groundcoat enamel one or more high melting point (refractory) materials, such as a ceramic of portland cement clinkers, mica flakes, slag glass and the like. The composition of a typical alkali-resistant groundcoat enamel for steel is shown in Table 1.
    TABLE 1
    Composition of a typical alkali-resistant
    groundcoat enamel for steel
    Amount
    Constituent (%)
    Silicon dioxide (SiO2) 42.02
    Boron oxide (B2O3) 18.41
    Sodium oxide (Na2O) 15.05
    Potassium oxide (K2O) 2.71
    Lithium oxide (Li2O) 1.06
    Calcium oxide (CaO) 4.47
    Aluminum oxide (Al2O3) 4.38
    Zirconium oxide (ZrO2) 5.04
    Copper oxide (CuO) 0.07
    Manganese dioxide (MnO2) 1.39
    Nickel oxide (NiO) 1.04
    Cobalt Oxide (Co3O4) 0.93
    Phosphorous Pentoxide (P2O5) 0.68
    Fluorine (F2) 2.75
  • In select embodiments of the present invention, a method for improving a bond between reinforcing material and a matrix incorporating the reinforcing material, comprises: selecting one or more flowable frits, such as an alkali-resistant groundcoat enamel, the frits compatible with the matrix and reinforcing material; selecting refractory material compatible with the matrix, reinforcing material and frits; mixing the refractory material with the frits to yield one or more coatings (glazes); preparing one or more surfaces of the reinforcing material; applying one or more coatings (glazes) to the surfaces; selecting a temperature regime for firing the coatings (glazes) onto the reinforcing material; selecting a time regime for conducting the firing; firing the coatings (glazes) on the reinforcing material at the selected temperature regime for the selected time regime; cooling the resultant coated (glazed) reinforcing material; inserting the resultant cooled reinforcing material into the matrix while the matrix is flowable, and curing the resultant reinforced flowable matrix.
  • In select embodiments of the present invention, a method for reinforcing a matrix by incorporating an enhanced reinforcing material therein, comprises: selecting one or more flowable frits compatible with the matrix and the reinforcing material; selecting refractory material compatible with the matrix, the reinforcing material and the frits; mixing the refractory material with the frits to yield one or more coatings (glazes); preparing one or more surfaces of the reinforcing material; applying one or more of the coatings (glazes) to the surfaces; selecting a temperature regime for firing the coatings (glazes) onto the reinforcing material; selecting a time regime for conducting the firing; firing the coatings (glazes) on the reinforcing material at the selected temperature and time regimes; cooling the resultant coated (glazed) reinforcing material; inserting the resultant cooled coated (glazed) reinforcing material into the matrix while the matrix is flowable, and curing the resultant reinforced flowable matrix.
  • In select embodiments of the present invention, a method for producing an enhanced reinforcing material for incorporating in a matrix comprises: selecting one or more flowable frits compatible with the matrix and a base reinforcing material; selecting refractory material compatible with the matrix, the base reinforcing material and the frits; mixing the refractory material with the frits to yield one or more coatings (glazes); preparing one or more surfaces of the base reinforcing material; applying one or more of the coatings (glazes) to one or more of the surfaces; selecting a temperature regime for firing the coatings (glazes) onto the reinforcing material; selecting a time regime for conducting the firing; firing the coatings (glazes) on the reinforcing material at the selected temperature and time regimes and cooling the resultant coated (glazed) reinforcing material.
  • In select embodiments of the present invention, a configuration is affixed to a base reinforcing material for improving the bond between the base reinforcing material and an initially flowable matrix incorporating the enhanced reinforcing material. The configuration comprises one or more flowable frits compatible with the matrix and the base reinforcing material and refractory material compatible with the matrix, the base reinforcing material and the frits, such that: the refractory material is mixed with the frits to yield one or more coatings (glazes); one or more surfaces of the reinforcing material are prepared for accepting the coatings (glazes); one or more coatings (glazes) are applied to the prepared surfaces, the coatings (glazes) are fired on the reinforcing material during a pre-specified temperature regime and for a pre-specified time regime; the resultant coated (glazed) reinforcing material is cooled; the resultant cooled enhanced reinforcing material is inserted into the matrix while the matrix is flowable and the resultant reinforced flowable matrix is cured.
  • In select embodiments of the present invention, an enhanced reinforcing structure for improving bonding of the enhanced reinforcing structure to a matrix incorporating the enhanced reinforcing structure comprises: one or more base reinforcing materials, each having one or more surfaces suitable for coating; one or more flowable frits compatible with the matrix and the base reinforcing materials and refractory material compatible with the matrix, the base material and the frits, such that: the refractory material is mixed with the frits to yield one or more coatings (glazes); one or more surfaces of the base material are prepared for accepting the coatings (glazes); one or more coatings (glazes) are applied to one or more of the prepared surfaces; one or more of the coatings (glazes) are fired onto one or more of the surfaces during a pre-specified temperature regime over a pre-specified time regime; the resultant enhanced reinforcing structure is cooled; the resultant cooled enhanced reinforcing structure is inserted into the matrix while the matrix is flowable and the resultant flowable matrix incorporating enhanced reinforcement is cured.
  • In select embodiments of the present invention, surfaces of the base reinforcing material are prepared for coating by cleaning and degreasing.
  • In select embodiments of the present invention, the base reinforcing material is selected from the group consisting of: metal fibers, metal rods, steel fibers, steel rods, metal alloy fibers, metal alloy rods, metal, metal alloys, steel, stainless steel, aluminum, copper, material plated with metal, and combinations thereof.
  • In select embodiments of the present invention, steels that may be used are selected from the group consisting of: low-carbon steel; decarburized steel; interstitial-free steel, i.e., steels in which carbon and nitrogen are contained in an alloying element such as titanium, niobium, vanadium and the like; titanium-stabilized steel, and combinations thereof.
  • In select embodiments of the present invention, the initially flowable matrix is a cement-based paste selected from the group consisting of: portland cement-based mortars; portland cement-based concretes; phosphate-cement based mortars; phosphate-cement based concretes; aluminum silicate cement-based mortars; aluminum silicate cement-based concretes, and combinations thereof.
  • In select embodiments of the present invention, frits are selected from the group consisting of: a ground glass, a ground glass slag, a frit suspended in a liquid, a glass frit suspended in a liquid, a powdered frit, a powdered glass frit, a frit containing transition metals, a frit containing cobalt, a frit containing nickel, an alkali-resistant glass frit, and combinations thereof.
  • In select embodiments of the present invention, coatings (glazes) comprise approximately equal amounts by volume of a frit and a refractory material. In select embodiments of the present invention, the frit may be a powdered glass frit and the refractory material dry portland cement, such as a type I-II portland cement. In select embodiments of the present invention, the dry portland cement may be provided in a proportion of up to about 70% by volume of the final mix. In select embodiments of the present invention, the coating (glaze) may comprise a frit suspended in a liquid and a dry refractory material in approximately equal amounts by volume of the liquid suspension and the refractory material. In select embodiments of the present invention, the coating (glaze) may comprise equal amounts by volume of a liquid suspension of an alkali-resistant glass frit and dry portland cement, such as a type I-II portland cement. In select embodiments of the present invention, the liquid suspension of an alkali-resistant glass frit may be a commercially available enamel groundcoat.
  • Surfaces are typically prepared for groundcoat enameling using an acid etch/nickel deposition preparation process. One such process is described in Porcelain Enameling, reprinted from Metals Handbook, Volume 5, ASM Committee on Porcelain Enameling, “Nonmetallic Coating Processes,” Porcelain Enameling American Society for Metals, 1995, with permission of the American Society of Metals, by Porcelain Enamel Institute, Inc., Nashville, Tenn., pp 459-460. The acid etch/nickel deposition process involves placing components to be coated (glazed) on corrosion-resistant racks and either dipping or spraying the parts with various solutions in a prescribed order and for a prescribed time regime at each step.
  • Specifically, the steps are:
      • 1). Clean with an alkaline cleaner using a 2-step process for spray cleaning
      • 2). Warm rinse with water
      • 3). Cold rinse with water
      • 4). Pickle in a warm dilute sulfuric acid solution
      • 5). Cold rinse in a cold dilute sulfuric acid solution
      • 6). Deposit nickel
      • 7). Cold rinse in a cold dilute sulfuric acid solution
      • 8). Neutralize with a suitable liquid solution having a basic pH
  • Table 2, as provided in Porcelain Enameling, establishes specific ranges for the above Table 2, as provided in Porcelain Enameling, establishes specific ranges for the above process.
    TABLE 2
    Ground-Coat Enameling, Acid-etch/Nickel-deposition Process.
    Cycle time (min)
    Step Solution Composition ° C. Dip Spray
    1 Alkaline  15-60 g/L b Ambient  6-12 1-3
    Cleaner a to 100 c
    2 Warm Rinse Water 49-60 0.5-4   0.5-1  
    3 Cold Rinse Water Ambient 2-4 0.5-1  
    4 Pickle d H2SO4, 6-8% 66-71  5-10 3-5
    5 Cold Rinse Water, H2SO4 e Ambient 0.5-4   0.5-1  
    6 Nickel NiSO4 6 H2O, 60-82  5-10 4-6
    deposition f 5.6-7.5 g/L
    7 Cold rinse Water, H2SO4 e Ambient 0.5-4   0.5-1  
    8 Neutralize ⅔ Na2CO3, Ambient 1-6 1-2
    ⅓ borax,
    0.6-2.1 g/L

    a For spray cleaning, use a two-stage process.

    b For spray cleaning, use 3.8-15 g/L.

    c 60-82° C. for spray cleaner.

    d Weight loss of metal is 3-5 g/m2.

    e Maintain a pH in the solution of 3-3.5 to prevent formation of ferric iron.

    f Nickel deposit should be 0.2-0.6 g/m2; continuous filtration is used to remove Fe(OH)3.
  • After drying at 93-150° C., steel parts treated with this process have a light straw color. When low-carbon decarburized steel is enameled in a direct operation, the steel is etched to remove 11-22 g/m2 of surface metal and receives a surface deposit of 0.9-1.3 g/m2 of nickel. A ferric sulfate etching solution is sometimes used with decarburized steel.
  • In select embodiments of the present invention, coatings (glazes) are applied via a method selected from the group consisting of: spraying, dipping, brushing, flowing on, electrostatic spraying, rolling, and combinations thereof.
  • In select embodiments of the present invention, the temperature regime involves inserting the coated (glazed) reinforcing material into an oven pre-heated to the final temperature of said firing. In select embodiments of the present invention, the final temperature of firing the coating (glaze) is from about 500° C. to about 900° C., and preferably from about 800° C. to about 875° C.
  • In select embodiments of the present invention, the time regime is that time after inserting the coated (glazed) reinforcing material into an oven pre-heated to the final temperature of firing until removal of the fired reinforcing material from the oven. In select embodiments of the present invention, the time of firing is selected to be from about two minutes to about 45 minutes and preferably from about 15 minutes to about 30 minutes.
  • In select embodiments of the present invention, cooling of the fired reinforcing material is done by removing the fired reinforcing material from the oven and permitting the reinforcing material to reach ambient temperature in ambient air.
  • In select embodiments of the present invention, portland cement is employed as both the refractory material to be mixed with a frit and at least part of the composition of the matrix to be reinforced. Portland cement-based concrete begins as a strong alkaline paste. This paste varies in pH from about the pH of calcium hydroxide (12.5) to almost 14 depending on the amount of sodium present. This high alkalinity dictates selection of a frit that is alkali-resistant. Typically, alkali-resistant glass is made by adding zirconium to the basic silica-sodium-borate composition. Further, when a highly alkaline paste attacks glass, it typically forms a gel that tends to swell unless the gel is stabilized with a lithium compound. Existing alkali-resistant glass frits are made with both zirconium and lithium, thus, for a portland cement-based matrix, frits are selected from among existing (commercial) alkali-resistant frits. Some examples include “Cermet” from Thompson Enamel Co., Bellevue, Ky.; “Frit 2680 Transparent,” also from Thompson; and “F-579 Frit” from Fusion Ceramics, Inc., Carrollton, Ohio.
  • In select embodiments of the present invention, one or more flowable frits are mixed with one or more refractory materials (i.e., those inorganic materials having a melting point higher than that of the frits) such as portland cement clinkers, mica flakes, and the like. The resultant mixture is compatible with an embedding matrix, such as a portland cement-based mortar, in which the enhanced reinforcing material is to be inserted. In addition to improving the bond between the base reinforcing material and the matrix, the “frit-bonding” coating (glazing) may eliminate or reduce the rate of corrosion of metal or metal-plated reinforcement coated with it in accordance with an embodiment of the present invention.
  • In select embodiments of the present invention, at least three approaches exist for establishing an improved bond of a matrix to reinforcement material embedded in the matrix. First, the embedding matrix, such as a portland cement-based concrete or mortar paste, may be designed to etch, and thus bond with a particular established glass coating (enamel) on a reinforcement, such as rebar. Second, the glass (enamel) coating on the reinforcement material may be abraded to form a rough (more chemically active) surface and a dry “powdered” refractory material, such as portland cement or glass slag and the like, applied to the roughened surface to enhance the bond of the reinforcement to a structural matrix, such as portland cement-based mortar or concrete. Third, a preferred approach of select embodiments of the present invention, flowable frit materials may be mixed with a refractory material to yield a coating mixture (glaze) that is subsequently applied to the surface of a base reinforcement material and fired. The resultant coated (glazed) reinforcement material is permitted to cool and then inserted in an initially flowable matrix, such as a paste of a portland cement-based mortar or concrete.
  • In select embodiments of the present invention, equal volumes of a ground glass frit, preferably an alkali-resistant frit, and portland cement are mixed to prepare a mixture to be used as a “bonding-frit” coating (glaze). In select embodiments of the present invention, the glass may be a mixture of glass types such as are available from a recycling plant. More than 50% by volume portland cement may be used. In select embodiments of the present invention, up to about 70% by volume of the bonding-frit coating (glaze) may be portland cement. In select embodiments of the present invention, the texture of the resultant bonding-frit coating (glaze) mixture may range from a fine sand, such as a quartz sand, to a fine powder, such as portland cement.
  • In select embodiments of the present invention, a “ground glass” bonding-frit coating (glaze) is applied by making a slurry of the mixture of ground glass and portland cement using water or water mixed with a thickener or adhesive, such as methyl cellulose. The base reinforcing item, such as a steel rebar, may be coated by dipping, spraying, brushing, rolling or flow coating the slurry onto the surface. The resultant wet coating is typically air-dried prior to firing. In select embodiments of the present invention, the bonding-frit coating mixture may be applied in its dry state by electro-static spray such as any of the methods used in commercial powder coating.
  • Further, the method may be used to strongly bond two pieces of material each incorporating a rough (bumpy) enameled surface, prepared in accordance with embodiments of the present invention, at the interface to be joined. The two pieces may be joined by applying a suitable matrix, such as a portland cement-based grout, as an adhesive.
  • In select embodiments of the present invention, a method of enhancing bonding between surfaces of materials comprises: selecting one or more first and one or more second surfaces to be bonded; selecting one or more first flowable frits compatible with materials comprising the first surfaces; selecting first refractory material compatible with the first surfaces and the first frits; mixing the first refractory material with the first frits to yield one or more first coatings; preparing the first surfaces; applying one or more first coatings to the first surfaces; selecting one or more second flowable frits compatible with the materials comprising the second surfaces; selecting second refractory material compatible with the second surfaces and the second frits; mixing the second refractory material with the second frits to yield one or more second coatings; preparing the second surfaces; applying the second coatings to the second surfaces; selecting one or more temperature regimes for firing each of the first and second coatings onto the first and second surfaces, respectively; selecting a time regime for conducting each of the firings of the first and second coatings; firing the first and second coatings onto the first and second surfaces respectively at the selected temperature regimes for the duration of the selected time regimes; cooling the fired first and second surfaces; applying one or more grouts to one or more of the first and second fired surfaces; bringing one or more of the grouted surfaces in contact with one or more of the ungrouted surfaces to effect a bond between the first and second surfaces; and curing the grout.
    • EXAMPLE I
  • In laboratory tests, the bonding-frit coating (glaze) was prepared by mixing about 50% by volume of a portland cement type I-II with a 50% by volume of a commercial alkali-resistant ground coat enamel to yield a frit-bonding liquid coating. In select testing, this coating was applied to the experimental rods and fired at temperatures from about 805-870° C. At this temperature range, heat exposure ranged from about 2-12 minutes. The goal was to produce a final coating (glaze) that is about 50-100 μm (2-4 mils) thick, including the refractory material embedded therein. Thin spots were corrected by applying more bonding-frit coating (glaze) at the thin areas and firing a second time.
    • EXAMPLE II
  • Two sets of smooth (un-deformed) AISI C1018 steel rods, 72 mm in length and 6.35 mm in diameter, were treated in accordance with a method of an embodiment of the present invention. Unmodified rods were threaded at one end and used as a control. These control rods (threaded version not shown separately) were cleaned with oxalic acid and water, rinsed with tap water, rinsed with dilute sulfuric acid, rinsed with distilled water, and given a final rinse of alcohol and allowed to air dry.
  • The surfaces of experimental steel rods “enhanced” in accordance with an embodiment of the present invention were prepared by: cleaning with an alkali-based solution; water rinsing preferably with warm water (in a range of about 45-60° C.); water rinsing, preferably with cold water (ambient, i.e., about 15-25° C.); acid-etching in a sulfuric acid solution of about 6-8%; cold rinsing with a dilute sulfuric acid solution of pH of about 3.0-3.5; nickel deposition at about 0.02 to 0.06 g/m2 as described above from Porcelain Enameling; cold rinsing in a dilute sulfuric acid solution of pH about 3.0-3.5; and final rinsing in a sodium carbonate/sodium borate solution.
  • Refer to FIG. 1 describing the control and experimental rods used, where L1=65 mm, L=72 mm and D=6.5 mm. All rods 10 were threaded for about 7 mm (L−L1) of their length, L, similar to threading 21 of FIG. 2. The rods 10 were threaded to facilitate “pull out” testing.
  • Refer to FIG. 2 depicting a photograph of one of the coated (glazed) and fired experimental rods 20. None of the experimental rods 20 were abraded. The experimental rods were dipped into a water-based suspension of commercial glass frit (VitrearcTransparent Prussian Blue Cat. No. 2680, Thompson-Enamel Co., Bellevue, Ky.), portland cement (PC) type I-II, and methyl cellulose thickener (Klyr-Fire #A-1, Thompson-Enamel Co., Bellevue, Ky.). After coating (glazing) with the frit-bonding coating (glaze), the experimental rods 20 were permitted to air-dry and then fired in an electric furnace, resulting in a finished product 20 as represented in FIG. 2. After firing, the experimental rods 20 were allowed to air cool. Portions of the resultant fired frit-bonded coating (glaze) 22 are portland cement embedded in a cobalt-doped blue glass and appear as light-colored areas 23 in the “frit-bonding” coating (glaze) 22. The furnace temperature for the rod 20 photographed in FIG. 2 was 816° C., maintained for 30 minutes. For other experimental rods 20, the rods 20 were maintained at 745° C. for approximately 15 minutes.
  • The rods 10, 20 were inserted to a depth of 65 mm in a 76 mm (3 in) diameter, 152 mm (6 in) long cylinder containing a portland cement-based mortar paste. The standard mortar described in the ASTM C 109 section on proportioning was used to prepare the mortar cylinders. After the rods 10, 20 were inserted in the mortar paste; each cylinder was consolidated by vibrating the mortar paste for thirty seconds. All cylinders were moist-cured for seven days.
  • Refer to FIG. 3, a photograph of a section 31 of a typical cylinder split lengthwise along one side of the inserted rod 30. In this photo, the rod 30 has been extracted in the direction of the arrow 34 only a short distance as indicated at the arrow 32 to show a small portion of the void 33 resultant from extraction. FIG. 3 also shows how the experimental rod 30 was stripped completely of its coating (glaze) 22.
  • Refer to FIG. 4, a view of the mortar section 31 of FIG. 3 with the rod 30 removed completely. The darkened area is the entire void 33 showing the fired glaze 22 remaining attached within the mortar matrix 31 after the experimental rod 30 was pulled out, i.e., the bond of the fired frit-bonding coating (glaze) 22 to the mortar section 31 was stronger than the bond of the coating (glaze) 22 to the steel rod 30.
  • After moist curing, the adhesion between the mortar and the rods 10, 20 was determined by measuring the peak load required to pull the rods free from the mortar such that peak load equaled break load. The results of the testing are presented in Table 3. The load required for pull-out was measured by using an MTS Material Testing System (Minneapolis, Minn.).
    TABLE 3
    Results of Pull-out Test of Steel Rods in Moist-Cured Mortar
    Break Load
    Specimen (lbf)
    Control #1 735.9
    Control #2 136.8
    Control #3 749.4
    Control #4 929.7
    Mean 638.0
    Std Deviation 345.6
    Frit #1 w/PC (700° C.) 1927.0
    Frit #2 w/PC (700° C.) 1936.3
    Frit #3 w/PC (700° C.) 1441.5
    Mean 1768.3
    Std Deviation 283.0
  • Results for the control rods 10 were similar to those obtained with earlier tests with similar uncoated rods. The greatest adhesion between the experimental rods 20 and the mortar 31 was noted with the experimental rods 20 that were treated with a coating (glaze) containing a frit-bonding mixture of a glass frit and portland cement, i.e., a coating (glaze), that was fired on the rod 20. Coating with the “frit-bonding” coating mixture (glaze) of a portland cement type I-II and glass frit and firing the resultant coating (glaze) produced adhesion that was nearly three times greater than that measured for the control rods 10.
  • In select embodiments of the present invention, the frit-bonding coating (glaze) incorporating a commercial glass frit and portland cement performs better than the fusing of portland cement to an established enamel or abrading enamel and fusing portland cement thereto, the latter two described above as approaches one and two, respectively.
  • In summary, investigation proved that it is possible to bond grains of portland cement in mortar paste to portland cement grains, or any refractory mineral phases such as mica or quartz, that are bonded to steel. The bond thus achieved significantly improves the steel reinforcement of conventional concrete structures such as roadways, bridge decks, foundations, and the like.
  • The abstract of the disclosure is provided to comply with the rules requiring an abstract that will allow a searcher to quickly ascertain the subject matter of the technical disclosure of any patent issued from this disclosure. It is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims. 37 CFR § 1.72(b). Any advantages and benefits described may not apply to all embodiments of the invention.
  • While the invention has been described in terms of some of its embodiments, those skilled in the art will recognize that the invention can be practiced with modifications within the spirit and scope of the appended claims. For example, although the system is described in specific examples for improving the bond of reinforcement in cement-based matrices, it may apply to any number of applications including structure that may not employ a cement-based matrix but that does utilize reinforcement bonded thereto. In the claims, means-plus-function clauses are intended to cover the structures described herein as performing the recited function and not only structural equivalents, but also equivalent structures. Thus, although a nail and a screw may not be structural equivalents in that a nail employs a cylindrical surface to secure wooden parts together, whereas a screw employs a helical surface, in the environment of fastening wooden parts, a nail and a screw may be equivalent structures. Thus, it is intended that all matter contained in the foregoing description or shown in the accompanying drawings shall be interpreted as illustrative rather than limiting, and the invention should be defined only in accordance with the following claims and their equivalents.

Claims (43)

1. A method for producing an enhanced reinforcing material for incorporating in an initially flowable matrix, comprising:
providing base reinforcing material;
selecting one or more flowable frits compatible with said matrix and said base reinforcing material;
selecting refractory material compatible with said matrix, said base reinforcing material and said frits;
mixing at least one said refractory material with at least one said frits to yield at least one coating;
preparing at least one surface of said base reinforcing material;
applying one or more of said coatings to said surfaces;
selecting at least one temperature regime for firing said coatings onto said base reinforcing material;
selecting at least one time regime for conducting said firing;
firing at least one said coatings onto said base reinforcing material at said selected temperature regime for said selected time regime; and
cooling said enhanced reinforcing material.
2. The method of claim 1 preparing said base reinforcing material by cleaning and degreasing said surfaces.
3. The method of claim 2 further comprising preparing said surfaces by:
cleaning with an alkaline cleaner;
then rinsing with water at temperature between about 45 and 60° C.;
then rinsing with water provided at ambient temperature;
then pickling in a dilute sulfuric acid solution of about 66-71° C.;
then rinsing in a dilute sulfuric acid solution provided at ambient temperature;
then depositing nickel via a nickel-containing solution held between about 60 and 82° C.;
then rinsing in a dilute sulfuric acid solution provided at ambient temperature; and
then neutralizing with a suitable fluid solution having a pH above 7.0.
4. The method of claim 1 providing said base reinforcing material selected from the group consisting of: metal fibers, metal rods, steel fibers, steel rods, metal alloy fibers, metal alloy rods, metal, metal alloys, steel, stainless steel, aluminum, copper, material plated with metal, and combinations thereof.
5. The method of claim 4 providing said steel, steel fibers and steel rods selected from the group consisting of: low-carbon steel; decarburized steel; interstitial-free steel, titanium-stabilized steel, and combinations thereof.
6. The method of claim 1 providing said initially flowable matrix as cement-based pastes selected from the group consisting of: portland cement-based mortars; portland cement-based concretes; phosphate-cement based mortars; phosphate-cement based concretes;
aluminum silicate cement-based mortars; aluminum silicate cement-based concretes, and combinations thereof.
7. The method of claim 1 providing said frit selected from the group consisting of: a ground glass, a ground glass slag, a frit suspended in a liquid, a glass frit suspended in a liquid, a frit suspended in a liquid incorporating a thickener, a powdered frit, a powdered glass frit, a frit containing transition metals, a frit containing cobalt, a frit containing nickel, an alkali-resistant glass frit, an alkali-resistant groundcoat enamel, and combinations thereof.
8. The method of claim 1 providing said refractory material from the group consisting of portland cement, slag, mica, quartz, inorganics having a melting point higher than said frits, and combinations thereof.
9. The method of claim 1 providing at least one said coatings as a mixture of at least one powdered glass frit and at least one dry refractory material.
10. The method of claim 9 providing at least one said coatings as a mixture of dry portland cement and a powdered alkali-resistant glass frit.
11. The method of claim 10 providing said powdered alkali-resistant glass frit in the form of at least one commercially available enamel groundcoat.
12. The method of claim 1 providing at least one said coatings as a mixture of at least one glass frit suspended in a liquid and at least one dry refractory material.
13. The method of claim 12 providing at least one said dry refractory material as dry portland cement and at least one said glass frit suspended in a liquid as an alkali-resistant glass frit.
14. The method of claim 13 providing said alkali-resistant glass frit suspended in a liquid as at least one commercially available enamel groundcoat.
15. The method of claim 1 providing at least one said coatings as a mix of a volume amount of said frits approximately equal to a volume amount of said refractory material, wherein each of said coatings comprises at least one said frit and at least one said refractory material.
16. The method of claim 1 providing at least one said coatings as a mixture of up to approximately 70% by volume of dry portland cement and as little as approximately 30% by volume of at least one powdered alkali-resistant glass frit.
17. The method of claim 1 applying said coating via a method from the group consisting of: spraying, dipping, brushing, flowing on, electrostatic spraying, rolling, and combinations thereof.
18. The method of claim I selecting said temperature regime as inserting said coated reinforcing material into an oven pre-heated to the final temperature of said firing.
19. The method of claim 18 selecting said final temperature of said firing from about 500° C. to about 900° C.
20. The method of claim 18 selecting said final temperature of said firing from about 800° C. to about 875° C.
21. The method of claim 1 selecting said time regime as that time after inserting said glazed reinforcing material into an oven pre-heated to the final temperature of said firing until removal of said reinforcing material from said oven.
22. The method of claim 21 selecting said time of said firing from about two minutes to about 45 minutes.
23. The method of claim of claim 21 selecting said time of said firing from about 15 minutes to about 30 minutes.
24. The method of claim 1 accomplishing said cooling by removing said fired reinforcing material from said oven and permitting said reinforcing material to reach ambient temperature in ambient air.
25. A method for improving a bond between enhanced reinforcing material and a matrix into which said enhanced reinforcing material is inserted prior to curing said matrix, comprising:
selecting at least one flowable frit compatible with said matrix and said reinforcing material;
selecting refractory material compatible with said matrix, said reinforcing material and said frits;
mixing said refractory material with said frits to yield at least one coating;
preparing at least one surface of said reinforcing material;
applying at least one said coating to said surfaces;
selecting a temperature regime for firing said coatings onto said reinforcing material;
selecting a time regime for conducting said firing;
firing said coatings onto said reinforcing material at said temperature regime for the duration of said time regime;
cooling said fired reinforcing material;
inserting said cooled reinforcing material into said matrix while said matrix is flowable, said cooled reinforcing material suitable to reinforce said matrix; and
curing said reinforced matrix.
26. A method for reinforcing a matrix that is initially flowable by incorporating enhanced reinforcement material therein, comprising:
selecting at least one flowable frit compatible with said matrix and said reinforcing material;
selecting refractory material compatible with said matrix, said reinforcing material and said frits;
mixing said refractory material with said frits to yield at least one coating;
preparing at least one surface of said reinforcing material;
applying at least one said coating to said prepared surfaces;
selecting a temperature regime for firing said coatings onto said reinforcing material;
selecting a time regime for conducting said firing;
firing said coated reinforcing material at said temperature regime over said time regime;
cooling said fired and glazed reinforcing material;
inserting said cooled reinforcing material into said matrix while said matrix is flowable, said cooled reinforcing material suitable to reinforce said matrix; and
curing said reinforced matrix.
27. A configuration affixed to reinforcing material for improving the bond between said reinforcing material and an initially flowable matrix incorporating said reinforcing material, comprising:
at least one flowable frit compatible with said matrix and said reinforcing material; and
refractory material compatible with said matrix, said reinforcing material and said frits,
wherein said refractory material is mixed with said frits to yield at least one coating, and
wherein at least one surface of said reinforcing material is prepared for accepting said coating, and
wherein at least one said coating is applied to said prepared surfaces, and
wherein said coating is fired on said reinforcing material during a pre-specified temperature regime and for a pre-specified time regime, and
wherein said fired reinforcing material is cooled, and
wherein said cooled reinforcing material is inserted into said matrix while said matrix is flowable, said cooled reinforcing material suitable to reinforce said matrix, and
wherein said reinforced matrix is cured.
28. The configuration of claim 27 in which said reinforcing material is material selected from the group consisting of: metal fibers, metal rods, steel fibers, steel rods, metal alloy fibers, metal alloy rods, metal, metal alloys, steel, stainless steel, aluminum, copper, material plated with metal, and combinations thereof.
29. The configuration of claim 28 in which said steel, steel fibers and steel rods are selected from the group consisting of: low-carbon steel; decarburized steel; interstitial-free steel, titanium-stabilized steel, and combinations thereof.
30. The configuration of claim 27 in which said initially flowable matrix comprises cement-based pastes selected from the group consisting of: portland cement-based mortars; portland cement-based concretes; phosphate-cement based mortars; phosphate-cement based concretes; aluminum silicate cement-based mortars; aluminum silicate cement-based concretes, and combinations thereof.
31. The configuration of claim 27 in which said frit is selected from the group consisting of: a ground glass, a ground glass slag, a frit suspended in a liquid, a glass frit suspended in a liquid, a frit suspended in a liquid incorporating a thickener, a powdered frit, a powdered glass frit, a frit containing transition metals, a frit containing cobalt, a frit containing nickel, an alkali-resistant glass frit, an alkali-resistant groundcoat enamel, and combinations thereof.
32. The configuration of claim 27 in which at least one said coatings is a mixture of at least one powdered glass frit and at least one dry refractory material.
33. The configuration of claim 27 in which at least one said coatings is a mixture of dry portland cement and a powdered alkali-resistant glass frit.
34. The configuration of claim 33 in which said powdered alkali-resistant glass frit is at least one commercially available enamel groundcoat.
35. The configuration of claim 27 in which at least one of said coatings is a mixture of at least one glass frit suspended in a liquid and at least one dry refractory material.
36. The configuration of claim 35 in which at least one said dry refractory material is dry portland cement and at least one said glass frit suspended in a liquid is an alkali-resistant glass frit.
37. The configuration of claim 36 in which said alkali-resistant glass frit suspended in a liquid is at least one commercially available enamel groundcoat.
38. The configuration of claim 27 in which at least one of said coatings is a mixture of a volume amount of said frits approximately equal to a volume amount of said refractory material,
wherein each of said coatings comprises at least one said frit and at least one said refractory material.
39. The configuration of claim 27 in which at least one of said coatings is a mixture of up to approximately 70% by volume of dry portland cement and as little as approximately 30% by volume of powdered alkali-resistant glass frit.
40. The configuration of claim 27 in which at least one said coating is applied via a method from the group consisting of: spraying, dipping, brushing, flowing on, electrostatic spraying, rolling, and combinations thereof.
41. A reinforcing structure for improving the bonding of said reinforcing structure to an initially flowable matrix incorporating said reinforcing structure, comprising:
at least one base material having at least one surface suitable for coating;
at least one flowable frit compatible with said matrix and said base material; and
refractory material compatible with said matrix, said base material and said frits,
wherein said refractory material is mixed with said frits to yield at least one coating, and
wherein at least one surface of said base material is prepared for accepting said coating, and
wherein at least one said coating is applied to said prepared surfaces, and
wherein said coatings are fired on said surfaces at a pre-specified temperature regime over a pre-specified time regime, and
wherein said resultant coated reinforcing structure is cooled, and
wherein said resultant cooled reinforcing structure is inserted into said matrix while said matrix is flowable, and
wherein the resultant reinforced flowable matrix is cured.
42. A method of enhancing bonding between surfaces of materials, comprising:
selecting at least one first and at least one second surfaces, at least one said first surface to be bonded to at least one said second surface;
selecting at least one first flowable fit compatible with said materials comprising said first surfaces;
selecting first refractory material compatible with at least said first surfaces and said first frits;
mixing said first refractory material with said first frits to yield at least one first coating;
preparing at least one first surface;
applying at least one said first coating to said first surfaces;
selecting at least one second flowable frit compatible with said materials comprising said second surfaces;
selecting second refractory material compatible with at least said second surfaces and said second frits;
mixing said second refractory material with said second frits to yield at least one second coating;
preparing at least one second surface;
applying at least one said second coating to said second surfaces;
selecting at least one temperature regime each for firing said first and second coatings onto said first and second surfaces, respectively;
selecting a time regime for conducting each of said firings of said first and second coatings;
firing said first and second coatings onto said first and second surfaces respectively at said temperature regimes for the duration of said time regimes;
cooling said fired first and second surfaces;
applying at least one grout to at least one said first and second fired surfaces;
bringing at least one said grouted surfaces in contact with at least one ungrouted surface to effect a bond between said first and second surfaces; and
curing said grout.
43. The method of claim 42 preparing said base reinforcing material by cleaning and degreasing said first and second surfaces.
US11/234,184 2005-09-26 2005-09-26 System and method for increasing the bond strength between a structural material and its reinforcement Abandoned US20070264527A1 (en)

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US12/793,799 US20100247860A1 (en) 2005-09-26 2010-06-04 Configuration for Increasing the Bond Strength Between a Structural Material and Its Reinforcement
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