US20070119715A1 - Corrosion Resistant Wire Products and Method of Making Same - Google Patents

Corrosion Resistant Wire Products and Method of Making Same Download PDF

Info

Publication number
US20070119715A1
US20070119715A1 US11/624,649 US62464907A US2007119715A1 US 20070119715 A1 US20070119715 A1 US 20070119715A1 US 62464907 A US62464907 A US 62464907A US 2007119715 A1 US2007119715 A1 US 2007119715A1
Authority
US
United States
Prior art keywords
wire
mesh
strands
electrogalvanizing
galvanizing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/624,649
Inventor
Abraham Sacks
Jeffrey Sacks
Harold Davis
William Spilchen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US11/287,051 external-priority patent/US20070119106A1/en
Application filed by Individual filed Critical Individual
Priority to US11/624,649 priority Critical patent/US20070119715A1/en
Publication of US20070119715A1 publication Critical patent/US20070119715A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04FFINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
    • E04F13/00Coverings or linings, e.g. for walls or ceilings
    • E04F13/02Coverings or linings, e.g. for walls or ceilings of plastic materials hardening after applying, e.g. plaster
    • E04F13/04Bases for plaster
    • E04F13/047Plaster carrying meshes
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/06Zinc or cadmium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/34Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
    • C23C2/36Elongated material
    • C23C2/38Wires; Tubes
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C22/00Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/24Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing hexavalent chromium compounds
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/02Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D7/00Electroplating characterised by the article coated
    • C25D7/06Wires; Strips; Foils
    • C25D7/0607Wires
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2222/00Aspects relating to chemical surface treatment of metallic material by reaction of the surface with a reactive medium
    • C23C2222/10Use of solutions containing trivalent chromium but free of hexavalent chromium

Definitions

  • This invention relates to wire products and in particular to fabricated wire products, such as welded or woven mesh, stucco corner reinforcements, barbed wire and wire fencing.
  • the zinc can be applied by hot galvanizing methods, by electro-galvanization, by sherardizing, by spraying, or by cold galvanizing methods.
  • the zinc protects the steel since it is less noble in the galvanic series of metals and hence will be sacrificed in a corrosive environment in relation to the steel. Since zinc is sacrificial, it will be consumed with time. The rate of zinc loss or consumption over time depends on the severity of the corrosive environment.
  • Zinc also has the further benefit that since it protects the steel by being sacrificial, small localized areas of bare steel are still protected by the adjacent zinc. This differs from the behavior of other protective coatings such as paint or chrome whereby any non-coated or scratched areas corrode quickly.
  • Zinc consumption rates can vary under different general atmospheric exposures, but have been evaluated by various researchers to be generally 0.06 oz./sq. ft. per year in rural atmospheres, 0.07 oz./sq. ft. per year in marine atmospheres, and 0.1 to 0.4 oz./sq. ft. per year in industrial areas.
  • the amount of zinc coating can be increased for specific applications or environments to provide a longer effective life.
  • Ranges of zinc coating weights are given in specifications such as ASTM A 641/A 641M-03 ‘Standard Specification for Zinc-Coated (Galvanized) Carbon Steel Wire’. Coating weights range from a low of 0.15 oz./sq. ft. for Class 1 wires up to a maximum of 3.00 oz./sq. ft. for Class C coating.
  • ASTM A653/A653M-05a ‘Standard Specification for Steel Sheet, Zinc-Coated (Galvanized) by the Hot-Dip Process” and provides standards for various zinc or zinc-iron alloy coating weights or coating designations.
  • the coating weight can be selected from such standards and specifications to best suit the intended application and expected life. Nonetheless, in the case of wire coatings, even at maximum zinc weights, life expectancy may range from 50 years to as little as 7.5 years.
  • the Zn-55 Al alloy exhibits good corrosion resistance, but does not provide satisfactory sacrificial protection of the steel substrate because of the high aluminum content. Further, weldability is very poor due to the high aluminum content. The process is further complicated by the need for expensive preliminary surface treatments, and even so has a tendency to form bare spots and similar defects. These deficiencies led to the development of improved coatings as disclosed in U.S. Pat. No. 4,448,748.
  • the coating bath contains zinc, 5% aluminum, and a mischmetal addition.
  • the term mischmetal refers to a variety of known rare earth alloys, such as cerium and lanthanum. This coating was developed by ILZRO (The International Lead-Zinc Research Organization), and is known in the trade as Galfan®.
  • Corrosion resistance of the Galfan® products is not quite as good as the original 55% Al—Zn coatings but the sacrificial aspect of the coating was improved. However, weldability is still a problem and surface preparation is still difficult. Normal zinc ammonium chloride fluxes cannot be used in the surface preparation, as would be the case with conventional hot galvanizing.
  • aluminized wire coatings when formed into products such as welded mesh for concrete reinforcement, showed very rapid corrosion in concrete, compared to pure zinc coatings, with the aluminized coating losing 95% of its coating weight in five years. In the same period, galvanized wire mesh loses only 40%. Cinders, fly ash, and lime found in concrete, mortar or stucco, in direct contact with aluminized steels is extremely corrosive.
  • Chromate conversion coatings are produced on various metals by chemical or electrochemical treatment with mixtures of hexavalent chromium and certain other compounds. These treatments react with the metal surface to provide a superficial layer containing a complex mixture of chromium compounds. Chromate conversion of zinc or cadmium coatings was first patented in 1936 by E. J. Wilhelm (U.S. Pat. No. 2,035,380).
  • Chromate coatings are usually applied to electroplated zinc coatings. A range of distinctive colors such as clear-blue, yellow, green or black can be obtained. The color differences are obtained by varying the chemical formulation and pH values. The darker colors indicate greater chromate thickness. Coating thickness can vary from 0.2 to 0.7 mils. Greater thickness also provides the greatest corrosion resistance. For example, salt spray tests show the following hours to red rust on zinc plated steel with and without chromate: 150 to 400 hours with no chromate, 250 to 750 hours with clear or bluish chromate, 250 to 1000 hours with yellow chromate, and 500 to 1500 hours with olive/khaki chromate. As can be seen, chromate coatings can enhance corrosion resistance by a factor of 2 to 4.
  • Chromate coatings are relatively inexpensive, can be applied quickly and can provide good corrosion enhancement as shown above. Protection is due to both the corrosion inhibiting effect of chromium compounds contained in the film, and to the physical barrier presented by the film itself. Even scratched or abraded films retain a great deal of their protective value, since the chromium content is slowly leachable in contact with moisture, providing a self healing effect.
  • chromate coatings are that they soft and easily damaged while wet. They become reasonably hard when dried, and can withstand normal handling and part assembly. However, they will not withstand continued scratching, abrasion, stamping or cold forming, such as is encountered in fabrication processes.
  • the terms “fabrication” and “fabricated” refer to mechanical steps that involve the manipulation of strands to change their relative positions, or their shapes or mechanical interrelationship. Examples of fabrication steps as understood herein are welding, weaving, rolling, reshaping, bending, cutting and twisting.
  • a second disadvantage of chromate coatings is that they only convert zinc coatings well when the zinc coatings are pure, with few contaminants.
  • a zinc coating obtained by hot dip galvanizing consists of several layers: an internal alloy of iron and zinc which adheres to the surface of the ferrous material, and an external layer, consisting almost entirely of pure zinc called the Eta phase.
  • an internal alloy of iron and zinc which adheres to the surface of the ferrous material
  • an external layer consisting almost entirely of pure zinc
  • the Eta phase In the interior layer, formed by the diffusion of zinc into the ferrous material, up to three zones or sub-layers can be distinguished, identified by their different iron contents.
  • the sub-layer closest to the base material is called the Gamma phase and contains 21 to 28% iron.
  • the next layer is the Delta phase, which contains from 6% to 11% iron, and finally the Zeta phase which contains approximately 6% iron.
  • iron contamination of the zinc coating causes black staining of the zinc coating when chromated.
  • the cause of this black staining is postulated to be the formation of black iron oxides as a result of reaction of hexavalent chromium compounds and iron deposits. Not only is the appearance of the black staining not attractive, but some of the corrosion enhancement is lost as well
  • Such products such as metal flashings, metal roofing, wire fencing, barbed wire, lath, welded wire fabrics and others, are fabricated from pre-galvanized sheet or wire.
  • the galvanizing may be damaged during fabrication. Zinc may be burned off during welding, and cut edges such as on barbed wire results in non galvanized areas.
  • Such products are nonetheless manufactured from pre galvanized feed stock since it would be extremely difficult and expensive to galvanize them after fabrication.
  • hot galvanizing offers distinct advantages. These include the fact that hot galvanizing is fast resulting in high production speeds, requires low capital investment and requires relatively little space. Adhesion of zinc is normally very good as a result of the alloying effect of the hot galvanizing process.
  • electro-galvanizing is a very efficient process. There is no dross or oxide formation and therefore virtually 100% of the zinc is plated onto the product. Further, coating weights can be exactly controlled to specification and there is no give away of zinc. With rapidly rising zinc costs, economics have swung in favor of electro-galvanizing. Unfortunately, the electro-galvanizing process is slow and coating weights are inversely proportional to line speed. In order to achieve a two-fold increase in coating weight, a production line needs to operate at half the speed. Further, with increased coating weight, zinc adhesion becomes more difficult such that zinc flaking may occur with mechanical deformation during fabrication of finished products. Therefore, electro-galvanizing can not take full economic advantage of the rising zinc costs in relation to hot galvanizing, and consequently the costs of all galvanized products are rising.
  • Stucco lath and stucco wire reinforcement products may be of the welded type or the woven type. These products are described in specifications ASTM C933-05 ‘Standard Specification for Welded Wire Lath’, ASTM C1032-06 ‘Standard Specification for Woven Wire Plaster Base’ and ASTM C1063-03 ‘Standard Specification for Installation of Lathing and Furring to Receive Interior and Exterior Portland Cement -Based Plaster’.
  • the wire must be Class 1 zinc coated (galvanized) soft temper steel material.
  • the wire sizes usually incorporated in these wire laths are 0.035 inch diameter to 0.053 inch diameter. Class 1 coatings for these size ranges specify a minimum 0.15 oz./sq. ft.
  • Corrosion resistance of stucco laths has become of increasing concern in the building industry over the last 10 years because of premature failures.
  • the Class 1 coating as specified is still considered to be a light zinc coating and is not intended for years of service in an outdoor environment.
  • the galvanized coating is intended to provide short term protection after the lath is produced but still not applied, while the lath is on the wall prior to stucco application, and while the stucco is wet and curing. Long term protection is provided by the stucco keeping the majority of moisture away from the wire. Installation instructions caution the installer to ensure that wire is covered with at least 1 ⁇ 8 inch of stucco.
  • these proprietary stuccos have various additives such as fly ash and a myriad of other chemical admixtures which can result in more aggressive stuccos when in contact with moisture.
  • the invention is a method of manufacturing fabricated wire products comprising welded or reverse twist woven wire mesh, comprising the steps of galvanizing wire strands prior to fabricating said mesh, fabricating the mesh from the galvanized wire strands and applying a chromate treatment to the fabricated wire mesh.
  • the wire strands are galvanized by hot galvanizing followed by electrogalvanizing.
  • the electrogalvanized layer is less than 0.10 oz./sq. ft.
  • the invention consists of welded or woven wire mesh manufactured according to the foregoing methods.
  • the invention consists of welded wire mesh comprising perpendicular strands of wire welded together at their intersections, wherein said strands comprise a first hot galvanized layer of zinc or zinc alloy and a second electrogalvanized layer, said second layer having been subjected to a chromate treatment.
  • FIG. 1 is a diagram of the first embodiment of the method of the invention
  • FIG. 1A is an enlarged cross-sectional view of a strand made according to the invention.
  • FIG. 2 is a diagram of the alternative embodiment of the method of the invention.
  • FIG. 2A is an enlarged cross-sectional view of a strand made according to the alternative embodiment of the invention.
  • FIG. 3 is illustrates the method of applying a chromate treatment to rolls of fabricated product according to the invention.
  • stucco lath 10 consists of welded wire mesh formed from strands 12 welded at their intersections 13 .
  • the strands 12 Prior to the fabrication steps 16 of forming the mesh and welding, the strands 12 have been galvanized with a galvanized zinc or zinc alloy coating 14 of less than 0.10 oz./sq. ft.
  • the galvanized coating is less than 0.05 oz./sq. ft.
  • the zinc is applied by electro-galvanization.
  • a chromate treatment 18 coating 16 is applied to provide a chromate coating 20 .
  • lath 10 has been exemplified as a welded wire mesh stucco lath, the invention applies equally to woven wire mesh lath, woven wire plaster base, or welded stucco corner reinforcement, wherein the fabrication may involve formation of the structure and bending, rolling, twisting or weaving steps.
  • a zinc-chromate layer is applied to areas that have been damaged during welding or mechanical twisting. It has been found that despite the presence of localized ungalvanized areas (due to trauma during fabrication), a post-fabrication chromate treatment seems to somehow repair the damaged areas, resulting in a significant increase in corrosion resistance even for such areas. Further to this benefit is the opportunity for cost savings through the use of less zinc to obtain equal or better corrosion resistance in comparison to higher zinc coating weights. This offers significant economic benefits.
  • FIGS. 2 and 2 A illustrate the steps according to an alternative embodiment.
  • welded wire stucco lath 22 is fabricated from strands 24 that were first hot galvanized ( 26 ) to produce a hot galvanized layer 28 , then treated ( 30 ) to provide an electro-galvanized coating 32 .
  • the lath is then fabricated ( 34 ) by forming the mesh into perpendicular strands 36 and 38 , and welding them at their intersections 13 as illustrated in FIG. 1 .
  • Other fabrication steps such as rolling to deform the nominally round shape of some of the strands, and bending may also be involved.
  • the lath Once the lath has been fabricated, it is subjected to a chromate conversion process 40 to produce a chromate layer 42 .
  • This embodiment has the advantage of utilizing the hot galvanization process which can rapidly apply the base zinc with good adhesion. A very thin electro-galvanized coating is then applied.
  • the benefits of this embodiment are that both the hot galvanizing and the electro-galvanizing can be accomplished in line at the wire galvanizing plant at high speed. This utilizes the positive attributes of each type of galvanizing.
  • the hot galvanization can be applied at high speeds, and since only a very thin electro-galvanized layer is called for in the invention, it can also be achieved at that same high speed. Since the outer layer is pure zinc as a result of the electro-galvanization, the chromate conversion is of good quality.
  • the zinc or zinc alloy coating applied by hot galvanization is between 0.08 and 0.20 oz/sq.ft. and the electro-galvanized layer is less than 0.10 oz/sq.ft. or less.
  • the hot galvanization is less than 0.10 oz./sq.ft. and the electro-galvanized layer isbetween 0.02 and 0.1 oz./sq.ft. and preferably about 0.05 oz./sq.ft.
  • the wires are generally round in cross section. In other embodiments, some or all of the wires could be shaped such as flattened, oval, square, rectangular, or fluted. Further, these shaped areas could be parallel with the longitudinal axis of the wire, or they may be twisted to form spirals. Shaped wire adds rigidity or stiffness to the products, and reduces overall weight These wires would also be formed from pre galvanized round wires, either hot galvanized, electro-galvanized, or a combination of hot and electro galvanized type (for the first alternative embodiment). Shaped wires within the various stucco products would have an even greater benefit with this new invention since the wires have to undergo primary deformation to create the shape prior to final fabrication into the finished product.
  • this new invention is of even greater benefit to shaped wires as compared to round wires.
  • the production of the various stucco laths is accomplished on high speed machinery.
  • the products are packaged either in rolls, in sheets or in bundles.
  • the chromating treatment can be applied in line as the products are being produced, or in a secondary line after the product is in the packaged form.
  • a web of welded lath or woven lath passes through the chromating process before final packaging.
  • corner reinforcement single lengths of the product pass through the chromating process.
  • rolls 44 of welded or woven lath pass through the chromating process 46 - 52 in batches after fabrication.
  • groups of sheets could similarly be processed. Corner reinforcements would pass through the chromate process in groups of individual corners stacked together. Since the corners are normally marketed in groups of ten, it would be desirable to process groups of ten through the chromating process.
  • the chromating process consists of a series of steps.
  • the first step 46 is an aqueous dip for removal of lubricants or corrosion inhibitors that have been applied either during the galvanizing process or during fabrication of the product.
  • This dip bath is a heated alkaline solution, preferably 160 to 180 deg. F.
  • the time in this bath can range from 30 to 60 seconds. This is followed by a cold water rinse 46 a.
  • the second step 48 is removal of zinc oxides.
  • This dip bath is a nitric acid solution, with acid concentrations preferably in the 0.25% to 0.5% by volume and at temperatures in the 70 deg.F to 80 deg.F. range.
  • the time in this bath is 1 to 5 seconds, to limit loss of zinc.
  • This step is also followed by a cold water rinse ( 48 a ).
  • the third step is the actual chromating step 50 in which the roll is submerged in a bath of an aqueous solution of either a hexavalent sodium chromate or a trivalent sodium chromate.
  • the temperature is from 70 deg.F. to 110 deg.F., but the preferred temperature would be 90 deg.F.
  • the preferred concentration is 1% by volume.
  • the time in this bath can range from 5 to 60 seconds.
  • the preferred time is 25 to 30 seconds. This is followed by a cold water rinse 50 a.
  • the cold water rinses serve to minimize the contamination of subsequent solutions. They also reduce the quantity of contaminated rinse solutions, which would have to be treated in a waste water treatment facility prior to discharge.

Abstract

Corrosion resistance is achieved for fabricated wire products such as welded or woven stucco mesh, by fabricating the products from pre-galvanized strands of wire, followed by a post-fabrication chromate treatment. In the preferred embodiment, the strands are pre-galvanized by a first hot galvanization step followed by applying a thin electro-galvanization layer.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a Continuation-In-Part of U.S. patent application Ser. No. 11/287,051 which was filed on Nov. 25, 2005.
  • FIELD OF THE INVENTION
  • This invention relates to wire products and in particular to fabricated wire products, such as welded or woven mesh, stucco corner reinforcements, barbed wire and wire fencing.
  • BACKGROUND OF THE INVENTION
  • Using zinc to protect steel from corrosion has been practiced for over 150 years. The zinc can be applied by hot galvanizing methods, by electro-galvanization, by sherardizing, by spraying, or by cold galvanizing methods. The zinc protects the steel since it is less noble in the galvanic series of metals and hence will be sacrificed in a corrosive environment in relation to the steel. Since zinc is sacrificial, it will be consumed with time. The rate of zinc loss or consumption over time depends on the severity of the corrosive environment. Zinc also has the further benefit that since it protects the steel by being sacrificial, small localized areas of bare steel are still protected by the adjacent zinc. This differs from the behavior of other protective coatings such as paint or chrome whereby any non-coated or scratched areas corrode quickly.
  • However, as the zinc is consumed, protection of the steel substrate is ultimately lost and corrosion of the steel begins to occur. Zinc consumption rates can vary under different general atmospheric exposures, but have been evaluated by various researchers to be generally 0.06 oz./sq. ft. per year in rural atmospheres, 0.07 oz./sq. ft. per year in marine atmospheres, and 0.1 to 0.4 oz./sq. ft. per year in industrial areas.
  • The amount of zinc coating can be increased for specific applications or environments to provide a longer effective life. Ranges of zinc coating weights are given in specifications such as ASTM A 641/A 641M-03 ‘Standard Specification for Zinc-Coated (Galvanized) Carbon Steel Wire’. Coating weights range from a low of 0.15 oz./sq. ft. for Class 1 wires up to a maximum of 3.00 oz./sq. ft. for Class C coating. Similarly, ASTM A653/A653M-05a ‘Standard Specification for Steel Sheet, Zinc-Coated (Galvanized) by the Hot-Dip Process” and provides standards for various zinc or zinc-iron alloy coating weights or coating designations.
  • The coating weight can be selected from such standards and specifications to best suit the intended application and expected life. Nonetheless, in the case of wire coatings, even at maximum zinc weights, life expectancy may range from 50 years to as little as 7.5 years.
  • Therefore, in the prior art, there have been various efforts to improve or increase the corrosion resistance of zinc coatings. One approach has been to coat steel substrates with aluminum-zinc coatings. Aluminum-zinc coatings, and the products of such coatings have been disclosed in U.S. Pat. Nos. 3,343,930, 3,393,089 and 3,952,120. It has been said that optimum corrosion resistance for such coatings occurs with a combination of 55% aluminum and 45% zinc and suppliers claim that 55% Al—Zn sheets will have a life from 30 to 40 plus years, except in severe marine applications, and at least twice the life of equal galvanized steels.
  • The Zn-55 Al alloy exhibits good corrosion resistance, but does not provide satisfactory sacrificial protection of the steel substrate because of the high aluminum content. Further, weldability is very poor due to the high aluminum content. The process is further complicated by the need for expensive preliminary surface treatments, and even so has a tendency to form bare spots and similar defects. These deficiencies led to the development of improved coatings as disclosed in U.S. Pat. No. 4,448,748. The coating bath contains zinc, 5% aluminum, and a mischmetal addition. The term mischmetal refers to a variety of known rare earth alloys, such as cerium and lanthanum. This coating was developed by ILZRO (The International Lead-Zinc Research Organization), and is known in the trade as Galfan®. Corrosion resistance of the Galfan® products is not quite as good as the original 55% Al—Zn coatings but the sacrificial aspect of the coating was improved. However, weldability is still a problem and surface preparation is still difficult. Normal zinc ammonium chloride fluxes cannot be used in the surface preparation, as would be the case with conventional hot galvanizing.
  • Further, it has been found that aluminized wire coatings, when formed into products such as welded mesh for concrete reinforcement, showed very rapid corrosion in concrete, compared to pure zinc coatings, with the aluminized coating losing 95% of its coating weight in five years. In the same period, galvanized wire mesh loses only 40%. Cinders, fly ash, and lime found in concrete, mortar or stucco, in direct contact with aluminized steels is extremely corrosive.
  • Another prior art approach to enhance corrosion resistance of galvanized surfaces is the application of a chromate surface treatment. Chromate conversion coatings are produced on various metals by chemical or electrochemical treatment with mixtures of hexavalent chromium and certain other compounds. These treatments react with the metal surface to provide a superficial layer containing a complex mixture of chromium compounds. Chromate conversion of zinc or cadmium coatings was first patented in 1936 by E. J. Wilhelm (U.S. Pat. No. 2,035,380).
  • Chromate coatings are usually applied to electroplated zinc coatings. A range of distinctive colors such as clear-blue, yellow, green or black can be obtained. The color differences are obtained by varying the chemical formulation and pH values. The darker colors indicate greater chromate thickness. Coating thickness can vary from 0.2 to 0.7 mils. Greater thickness also provides the greatest corrosion resistance. For example, salt spray tests show the following hours to red rust on zinc plated steel with and without chromate: 150 to 400 hours with no chromate, 250 to 750 hours with clear or bluish chromate, 250 to 1000 hours with yellow chromate, and 500 to 1500 hours with olive/khaki chromate. As can be seen, chromate coatings can enhance corrosion resistance by a factor of 2 to 4.
  • Chromate coatings are relatively inexpensive, can be applied quickly and can provide good corrosion enhancement as shown above. Protection is due to both the corrosion inhibiting effect of chromium compounds contained in the film, and to the physical barrier presented by the film itself. Even scratched or abraded films retain a great deal of their protective value, since the chromium content is slowly leachable in contact with moisture, providing a self healing effect.
  • The disadvantages of chromate coatings are that they soft and easily damaged while wet. They become reasonably hard when dried, and can withstand normal handling and part assembly. However, they will not withstand continued scratching, abrasion, stamping or cold forming, such as is encountered in fabrication processes. In this disclosure and in the claims, the terms “fabrication” and “fabricated” refer to mechanical steps that involve the manipulation of strands to change their relative positions, or their shapes or mechanical interrelationship. Examples of fabrication steps as understood herein are welding, weaving, rolling, reshaping, bending, cutting and twisting.
  • A second disadvantage of chromate coatings is that they only convert zinc coatings well when the zinc coatings are pure, with few contaminants.
  • The two most common methods for commercial galvanization are hot galvanizing and electro-galvanizing.
  • In general, a zinc coating obtained by hot dip galvanizing consists of several layers: an internal alloy of iron and zinc which adheres to the surface of the ferrous material, and an external layer, consisting almost entirely of pure zinc called the Eta phase. In the interior layer, formed by the diffusion of zinc into the ferrous material, up to three zones or sub-layers can be distinguished, identified by their different iron contents. The sub-layer closest to the base material is called the Gamma phase and contains 21 to 28% iron. The next layer is the Delta phase, which contains from 6% to 11% iron, and finally the Zeta phase which contains approximately 6% iron.
  • In hot galvanizing of wire, it is common to wipe the wires as they exit the zinc bath to remove excess zinc and meet the lower coating weights that customers have specified. This wiping action removes the outer phases leaving primarily the Gamma phase, which is iron rich.
  • As pointed out in U.S. Pat. No. 4,171,231, iron contamination of the zinc coating causes black staining of the zinc coating when chromated. The cause of this black staining is postulated to be the formation of black iron oxides as a result of reaction of hexavalent chromium compounds and iron deposits. Not only is the appearance of the black staining not attractive, but some of the corrosion enhancement is lost as well
  • As a result, chromate conversion is usually not performed on hot galvanized surfaces, and is restricted to steel parts that have been electro-galvanized since the zinc coating is very pure.
  • Many products such as fasteners, hardware, stamped parts, nails, etc, are made from uncoated steel. Once fabricated, the product is then degreased, electro-galvanized and chromated. Since there is no post galvanizing fabrication, there is no damage to the galvanizing or chromating. In addition, there are typically no ungalvanized areas, since there is no further punching, cutting, welding that would result in ungalvanized surfaces.
  • However, post-fabrication galvanizing is not considered to be practical for many products where the bulkiness or shape of the finished product would make it uneconomical or impractical to galvanize after fabrication. Classic examples are welded and woven wire mesh such as is used for stucco lath. This problem is exacerbated in the global economy where semi-finished steel may be produced overseas, and shipment of unprotected steel would be difficult and costly.
  • Such products, such as metal flashings, metal roofing, wire fencing, barbed wire, lath, welded wire fabrics and others, are fabricated from pre-galvanized sheet or wire. However, the galvanizing may be damaged during fabrication. Zinc may be burned off during welding, and cut edges such as on barbed wire results in non galvanized areas. Such products are nonetheless manufactured from pre galvanized feed stock since it would be extremely difficult and expensive to galvanize them after fabrication. However, it would be ineffective to use pre-chromated galvanized steel since the chromate surface would itself be damaged during fabrication, and hence the chromating properties could not be assured on the finished products.
  • Further, the economics of galvanizing have been dramatically affected by recent rises in the price of zinc. To compound this problem, the hot galvanizing process inherently results in the wastage of zinc through the formation of zinc dross and zinc oxides. These losses can amount up to 50% of the zinc usage, especially with lighter zinc coating weights such as Class 1 wire. Further losses of zinc are experienced with difficulty in controlling coating weights. A certain amount of over galvanization can occur which increases the cost of production.
  • Despite the drawback that chromate conversion is viewed as not applicable to hot galvanized surfaces, hot galvanizing offers distinct advantages. These include the fact that hot galvanizing is fast resulting in high production speeds, requires low capital investment and requires relatively little space. Adhesion of zinc is normally very good as a result of the alloying effect of the hot galvanizing process.
  • Conversely, electro-galvanizing is a very efficient process. There is no dross or oxide formation and therefore virtually 100% of the zinc is plated onto the product. Further, coating weights can be exactly controlled to specification and there is no give away of zinc. With rapidly rising zinc costs, economics have swung in favor of electro-galvanizing. Unfortunately, the electro-galvanizing process is slow and coating weights are inversely proportional to line speed. In order to achieve a two-fold increase in coating weight, a production line needs to operate at half the speed. Further, with increased coating weight, zinc adhesion becomes more difficult such that zinc flaking may occur with mechanical deformation during fabrication of finished products. Therefore, electro-galvanizing can not take full economic advantage of the rising zinc costs in relation to hot galvanizing, and consequently the costs of all galvanized products are rising.
  • Although the present invention may be applied to many fabricated wire products, the primary application is for wire mesh stucco lathing and stucco wire corner reinforcement. Stucco lath and stucco wire reinforcement products may be of the welded type or the woven type. These products are described in specifications ASTM C933-05 ‘Standard Specification for Welded Wire Lath’, ASTM C1032-06 ‘Standard Specification for Woven Wire Plaster Base’ and ASTM C1063-03 ‘Standard Specification for Installation of Lathing and Furring to Receive Interior and Exterior Portland Cement -Based Plaster’. According to ASTM A641-03 ‘Standard Specification for Zinc-Coated (Galvanized) Carbon Steel Wire, the wire must be Class 1 zinc coated (galvanized) soft temper steel material. The wire sizes usually incorporated in these wire laths are 0.035 inch diameter to 0.053 inch diameter. Class 1 coatings for these size ranges specify a minimum 0.15 oz./sq. ft.
  • Corrosion resistance of stucco laths has become of increasing concern in the building industry over the last 10 years because of premature failures. The Class 1 coating as specified is still considered to be a light zinc coating and is not intended for years of service in an outdoor environment. The galvanized coating is intended to provide short term protection after the lath is produced but still not applied, while the lath is on the wall prior to stucco application, and while the stucco is wet and curing. Long term protection is provided by the stucco keeping the majority of moisture away from the wire. Installation instructions caution the installer to ensure that wire is covered with at least ⅛ inch of stucco.
  • However, there are a number of changes that have occurred that have resulted in rapid deterioration of the stucco laths. First has been the advent of acrylic finish coats. These finishes have the ability to diffuse water vapor but are much slower than previous cementitious finishes. Therefore, if any moisture gets behind the surface of the stucco, it takes a longer time to dry which results in available moisture for accelerated corrosion. Acrylic finishes are not as thick as cementitious and do not result in ⅛ inch of covering, especially at corners. A second contributor to accelerated corrosion is the shift to one coat stucco systems. These systems are all thin systems resulting in stucco thickness down to ⅜ inch. Further, these proprietary stuccos have various additives such as fly ash and a myriad of other chemical admixtures which can result in more aggressive stuccos when in contact with moisture. Thirdly are environmental exposures. More stucco clad structures are being built in non-typical stucco climates such as coastal areas subject to wind driven rains and salt air, and high humid areas such as Texas and Florida. Therefore, there is a growing focus of building officials, architects, engineers, contractors and home owners to build improved stucco claddings.
  • Therefore, there is a need to provide a method for improved corrosion resistance on galvanized steel products whilst minimizing the amount of zinc used. In particular it is an object of the present invention to provide improved corrosion resistance on galvanized fabricated wire mesh products such as lath and corner reinforcements.
  • It is further an object of the present invention to provide a method for enhanced corrosion protection of wire products such as welded and woven wire fabrics, welded and woven meshes, barbed wire, and woven wire fencing.
  • These and other objects of the invention will be better understood by reference to the detailed description of the preferred embodiments which follows.
  • SUMMARY OF THE INVENTION
  • In one aspect the invention is a method of manufacturing fabricated wire products comprising welded or reverse twist woven wire mesh, comprising the steps of galvanizing wire strands prior to fabricating said mesh, fabricating the mesh from the galvanized wire strands and applying a chromate treatment to the fabricated wire mesh.
  • In another aspect, the wire strands are galvanized by hot galvanizing followed by electrogalvanizing. In a more specific aspect, the electrogalvanized layer is less than 0.10 oz./sq. ft.
  • In another aspect the invention consists of welded or woven wire mesh manufactured according to the foregoing methods.
  • In another aspect, the invention consists of welded wire mesh comprising perpendicular strands of wire welded together at their intersections, wherein said strands comprise a first hot galvanized layer of zinc or zinc alloy and a second electrogalvanized layer, said second layer having been subjected to a chromate treatment.
  • The foregoing was intended as a broad summary only and of only some of the aspects of the invention. It was not intended to define the limits or requirements of the invention. Other and more particular aspects of the invention will be appreciated by reference to the detailed description of the preferred embodiment and to the claims.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The preferred embodiments will be described by reference to the drawings thereof in which:
  • FIG. 1 is a diagram of the first embodiment of the method of the invention;
  • FIG. 1A is an enlarged cross-sectional view of a strand made according to the invention;
  • FIG. 2 is a diagram of the alternative embodiment of the method of the invention;
  • FIG. 2A is an enlarged cross-sectional view of a strand made according to the alternative embodiment of the invention; and,
  • FIG. 3 is illustrates the method of applying a chromate treatment to rolls of fabricated product according to the invention.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • Referring to FIGS. 1 and 1A, in a first embodiment of the present invention, stucco lath 10 consists of welded wire mesh formed from strands 12 welded at their intersections 13. Prior to the fabrication steps 16 of forming the mesh and welding, the strands 12 have been galvanized with a galvanized zinc or zinc alloy coating 14 of less than 0.10 oz./sq. ft. Preferably the galvanized coating is less than 0.05 oz./sq. ft. In the preferred embodiment, the zinc is applied by electro-galvanization.
  • After the lath has been fabricated (at 16), a chromate treatment 18 coating 16 is applied to provide a chromate coating 20.
  • Although lath 10 has been exemplified as a welded wire mesh stucco lath, the invention applies equally to woven wire mesh lath, woven wire plaster base, or welded stucco corner reinforcement, wherein the fabrication may involve formation of the structure and bending, rolling, twisting or weaving steps.
  • Testing on products produced in accordance with the invention has shown that corrosion resistance is increased by 6 to 10 times in relation to products with a Class 1 coating. These tests were conducted in salt spray chambers in accordance with ASTM B117-03 ‘Standard Practice for Operating Salt Spray (Fog) Apparatus’. The onset of red rust failure is at damaged areas. In the case of the welded products, this is at the weld points where the zinc has been burned off. In the case of woven products, rust failure occurs at the twisted areas which have been in contact with the twister gears.
  • By applying the chromate conversion coating on the finished product after fabrication as described herein, a zinc-chromate layer is applied to areas that have been damaged during welding or mechanical twisting. It has been found that despite the presence of localized ungalvanized areas (due to trauma during fabrication), a post-fabrication chromate treatment seems to somehow repair the damaged areas, resulting in a significant increase in corrosion resistance even for such areas. Further to this benefit is the opportunity for cost savings through the use of less zinc to obtain equal or better corrosion resistance in comparison to higher zinc coating weights. This offers significant economic benefits.
  • FIGS. 2 and 2A illustrate the steps according to an alternative embodiment. According to this embodiment, welded wire stucco lath 22 is fabricated from strands 24 that were first hot galvanized (26) to produce a hot galvanized layer 28, then treated (30) to provide an electro-galvanized coating 32. The lath is then fabricated (34) by forming the mesh into perpendicular strands 36 and 38, and welding them at their intersections 13 as illustrated in FIG. 1. Other fabrication steps such as rolling to deform the nominally round shape of some of the strands, and bending may also be involved. Once the lath has been fabricated, it is subjected to a chromate conversion process 40 to produce a chromate layer 42. This embodiment has the advantage of utilizing the hot galvanization process which can rapidly apply the base zinc with good adhesion. A very thin electro-galvanized coating is then applied. The benefits of this embodiment are that both the hot galvanizing and the electro-galvanizing can be accomplished in line at the wire galvanizing plant at high speed. This utilizes the positive attributes of each type of galvanizing. The hot galvanization can be applied at high speeds, and since only a very thin electro-galvanized layer is called for in the invention, it can also be achieved at that same high speed. Since the outer layer is pure zinc as a result of the electro-galvanization, the chromate conversion is of good quality.
  • According to this alternative embodiment, the zinc or zinc alloy coating applied by hot galvanization is between 0.08 and 0.20 oz/sq.ft. and the electro-galvanized layer is less than 0.10 oz/sq.ft. or less. Preferably, the hot galvanization is less than 0.10 oz./sq.ft. and the electro-galvanized layer isbetween 0.02 and 0.1 oz./sq.ft. and preferably about 0.05 oz./sq.ft.
  • In each of the above embodiments, the wires are generally round in cross section. In other embodiments, some or all of the wires could be shaped such as flattened, oval, square, rectangular, or fluted. Further, these shaped areas could be parallel with the longitudinal axis of the wire, or they may be twisted to form spirals. Shaped wire adds rigidity or stiffness to the products, and reduces overall weight These wires would also be formed from pre galvanized round wires, either hot galvanized, electro-galvanized, or a combination of hot and electro galvanized type (for the first alternative embodiment). Shaped wires within the various stucco products would have an even greater benefit with this new invention since the wires have to undergo primary deformation to create the shape prior to final fabrication into the finished product. During this primary deformation, damage to the zinc surface may occur. As well, thinning of the zinc coating occurs since the surface area of the wire is increased, whilst the available zinc quantity remains the same. Therefore, this new invention is of even greater benefit to shaped wires as compared to round wires.
  • Although the preferred embodiments have been described in relation to welded wire mesh, the invention is also applicable to reverse twist woven wire mesh.
  • The production of the various stucco laths is accomplished on high speed machinery. The products are packaged either in rolls, in sheets or in bundles. In each of the embodiments, the chromating treatment can be applied in line as the products are being produced, or in a secondary line after the product is in the packaged form. In the former case, a web of welded lath or woven lath passes through the chromating process before final packaging. With corner reinforcement, single lengths of the product pass through the chromating process. In the secondary line case, rolls 44 of welded or woven lath pass through the chromating process 46-52 in batches after fabrication. In the case of sheet products, groups of sheets could similarly be processed. Corner reinforcements would pass through the chromate process in groups of individual corners stacked together. Since the corners are normally marketed in groups of ten, it would be desirable to process groups of ten through the chromating process.
  • In either the inline or secondary line approach, the chromating process consists of a series of steps. The first step 46 is an aqueous dip for removal of lubricants or corrosion inhibitors that have been applied either during the galvanizing process or during fabrication of the product. This dip bath is a heated alkaline solution, preferably 160 to 180 deg. F. The time in this bath can range from 30 to 60 seconds. This is followed by a cold water rinse 46 a.
  • The second step 48 is removal of zinc oxides. This dip bath is a nitric acid solution, with acid concentrations preferably in the 0.25% to 0.5% by volume and at temperatures in the 70 deg.F to 80 deg.F. range. The time in this bath is 1 to 5 seconds, to limit loss of zinc. This step is also followed by a cold water rinse (48 a).
  • The third step is the actual chromating step 50 in which the roll is submerged in a bath of an aqueous solution of either a hexavalent sodium chromate or a trivalent sodium chromate. The temperature is from 70 deg.F. to 110 deg.F., but the preferred temperature would be 90 deg.F. The preferred concentration is 1% by volume. The time in this bath can range from 5 to 60 seconds. The preferred time is 25 to 30 seconds. This is followed by a cold water rinse 50 a.
  • The preceding step is followed by a hot water dip 52. This bath aids in curing the coating and provides heat to aid in flash drying the product. For drying, temperatures above 200 deg.F. are advantageous. However, above 150 deg.F., the iridescent yellow coating will start to bleach and fade. Therefore, the preferred temperature of the hot water rinse is 150 deg.F. and the time in this bath can range from 1 to 2 minutes.
  • The cold water rinses serve to minimize the contamination of subsequent solutions. They also reduce the quantity of contaminated rinse solutions, which would have to be treated in a waste water treatment facility prior to discharge.
  • Another feature of the chromating treatment is the relative movement of the solutions and the product itself. It was found that when there was very little relative motion, the chromate coating was very uneven. Satisfactory coatings were obtained at the outer edges of the rolls or bundles, but there was no coating within the package. Conversely, when there was high relative motion or agitation, virtually no chromate coating was achieved since it was washed off as it was being formed.
  • Agitating the solution does not produce satisfactory results, since solution velocities will be higher around the outside of the roll or bundle and virtually zero through the product itself. This is a result of the density of wire creating a high resistance to liquid flow through the product. Therefore, again the chromate is not consistent throughout the product package.
  • Therefore, in the preferred embodiment, the product is moved within each of the baths. The preferred rate of motion is 3 inches per second to achieve optimum results. The rolls or bundles are mounted on hooks or racks, which are transported from tank to tank by a mechanized crane or conveyor 56 before being collected on a pallet 54. At each tank, the crane or conveyor stops for the appropriate dip time and oscillates the product either up and down or from side to side at the desired velocity.
  • It will be appreciated by those skilled in the art that the preferred and alternative embodiments have been described in some detail but that certain modifications may be practiced without departing from the principles of the invention.

Claims (36)

1. A method of manufacturing fabricated wire products comprising welded or reverse twist woven wire mesh, comprising the steps of:
1. galvanizing wire strands prior to fabricating said mesh;
2. fabricating said mesh from said galvanized wire strands; and,
3. applying a chromate treatment to said fabricated wire mesh.
2. The method of claim 1 wherein said step of galvanizing comprises electrogalvanizing said wire strands.
3. The method of claim 1 wherein said step of galvanizing comprises hot galvanizing said wire strands followed by electrogalvanizing said wire strands.
4. The method of claim 3 wherein said step of electrogalvanizing said wire strands comprises electrogalvanizing an outer layer of said wire strands at less than 0.10 oz./sq. ft.
5. The method of claim 1 wherein said mesh comprises at least portions of at least some of said wire strands that have a non-round cross-section.
6. The method of claim 5 wherein said step of galvanizing comprises electrogalvanizing said wire strands.
7. The method of claim 5 wherein said step of galvanizing comprises hot galvanizing said wire strands followed by electrogalvanizing said wire strands.
8. The method of claim 7 wherein said step of electrogalvanizing said wire strands comprises electrogalvanizing an outer layer of said wire strands at less than 0.10 oz./sq. ft.
9. Welded or reverse twist woven wire mesh manufactured according to the method of any of claims 1 to 8.
10. Welded wire mesh comprising perpendicular strands of wire welded together at their intersections, wherein said strands comprise a first hot galvanized layer of zinc or zinc alloy and a second electrogalvanized layer, said second layer having been subjected to a chromate treatment.
11. A method of manufacturing wire mesh, comprising providing wire mesh in rolled form, and applying a chromate treatment to said wire mesh while said wire mesh is in rolled form.
12. The method of claim 11 wherein said step of applying a chromate treatment comprises submerging said wire mesh in rolled form in a chromating solution.
13. The method of claim 12 wherein said chromating solution comprises an aqueous mixture containing hexavalent chromium.
14. The method of claim 12 wherein said chromating solution comprises an aqueous mixture containing trivalent chromium.
15. The method of claim 11 wherein said chromating treatment results in an iridescent yellow colour.
16. The method of claim 11, 12 or 13 wherein said wire mesh in rolled form is cleaned to remove an oxide layer therefrom prior to said step of applying a chromate treatment.
17. Wire mesh manufactured according to the method of any one of claims 11, 12, 13 or 14.
18. The method of claim 11 wherein said wire mesh in rolled form comprises portions of said mesh having strands with non-round cross sections.
19. The method of claim 11 wherein said wire mesh is selected from the group comprising welded wire mesh and reverse twist woven wire mesh.
20. The method of claim 19 further comprising the step of fabricating said wire mesh after said step of electrogalvanizing and applying a chromate treatment to said mesh after said step of fabricating.
21. Wire mesh manufactured according to the method of any one of claims 11 or 12 wherein said wire mesh is selected from the group comprising welded wire mesh and reverse twist woven wire mesh.
22. A method of manufacturing wire mesh comprising hot galvanizing wire, electrogalvanizing a thin layer over said hot galvanized wire, said hot galvanizing coating having a thickness between 0.08 oz./sq.ft. and 0.20 oz./sq.ft. and said electrogalvanizing having a thickness between 0.02 oz./sq.ft. and 0.10 oz./sq.ft.
23. The method of claim 22 further comprising the step of applying a chromate treatment to said wire mesh.
24. The method of claim 23 further comprising the step of fabricating said mesh from said wire after said step of electrogalvanizing and before said step of applying a chromate treatment.
25. A method of manufacturing welded wire corner reinforcements for stucco comprising the steps of:
galvanizing wire strands prior to fabricating a mesh;
fabricating said corner reinforcement from said mesh formed from said galvanized wire strands;
applying a chromate treatment to said fabricated corner reinforcement.
26. A welded wire corner reinforcement manufactured according to the method of claim 25.
27. The method of claim 25 wherein said step of galvanizing comprises electrogalvanizing said wire strands.
28. The method of claim 25 wherein said step of galvanizing comprises hot galvanizing said wire strands followed by electrogalvanizing said wire strands.
29. The method of claim 28 wherein said step of electrogalvanizing said wire strands comprises electrogalvanizing an outer layer of said wire strands at less than 0.10 oz./sq. ft.
30. The method of claim 25 wherein said mesh comprises at least portions of at least some of said wire strands that have a non-round cross-section.
31. The method of claim 30 wherein said step of galvanizing comprises electrogalvanizing said wire strands.
32. The method of claim 30 wherein said step of galvanizing comprises hot galvanizing said wire strands followed by electrogalvanizing said wire strands.
33. The method of claim 32 wherein said step of electrogalvanizing said wire strands comprises electrogalvanizing an outer layer of said wire strands at less than 0.10 oz./sq. ft.
34. Welded wire corner reinforcement for stucco comprising wire strands welded together at their intersections, wherein said strands comprise a first hot galvanized layer of zinc or zinc alloy, a second electrogalvanized layer of zinc, said second layer having been subjected to a chromate treatment.
35. Use of welded or reverse twist woven wire mesh manufactured according to the method of any one of claims 1 to 8 as stucco lath.
36. A building comprising a stucco surface, a stucco lath embedded in said surface, wherein said lath comprises mesh manufactured according to the method of any one of claims 1 to 8.
US11/624,649 2005-11-25 2007-01-18 Corrosion Resistant Wire Products and Method of Making Same Abandoned US20070119715A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/624,649 US20070119715A1 (en) 2005-11-25 2007-01-18 Corrosion Resistant Wire Products and Method of Making Same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11/287,051 US20070119106A1 (en) 2005-11-25 2005-11-25 Wire corner bead for stucco
US11/624,649 US20070119715A1 (en) 2005-11-25 2007-01-18 Corrosion Resistant Wire Products and Method of Making Same

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US11/287,051 Continuation-In-Part US20070119106A1 (en) 2005-11-25 2005-11-25 Wire corner bead for stucco

Publications (1)

Publication Number Publication Date
US20070119715A1 true US20070119715A1 (en) 2007-05-31

Family

ID=46327076

Family Applications (1)

Application Number Title Priority Date Filing Date
US11/624,649 Abandoned US20070119715A1 (en) 2005-11-25 2007-01-18 Corrosion Resistant Wire Products and Method of Making Same

Country Status (1)

Country Link
US (1) US20070119715A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102996975A (en) * 2012-12-17 2013-03-27 济南玫德铸造有限公司 Pipe fitting with double galvanized layers and manufacturing method thereof
TWI480538B (en) * 2013-05-21 2015-04-11 China Steel Corp Method of optically determining metallography of iron-zinc galvannealed intermetallic layer
US20150298158A1 (en) * 2014-04-22 2015-10-22 Metokote Corporation Zinc rich coating process
WO2019001872A1 (en) * 2017-06-29 2019-01-03 Nv Bekaert Sa Pre-stressed concrete structure with galvanized reinforcement

Citations (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2035380A (en) * 1933-05-13 1936-03-24 New Jersey Zinc Co Method of coating zinc or cadmium base metals
US2250508A (en) * 1936-06-15 1941-07-29 John S Thompson Treating zinc with organic acids
US2276353A (en) * 1935-09-28 1942-03-17 Parker Rust Proof Co Process of coating
US2327002A (en) * 1939-03-09 1943-08-17 Parker Rust Proof Co Coated article and method of making the same
US2393640A (en) * 1944-11-11 1946-01-29 Rheem Res Products Inc Dyed metals
US2485510A (en) * 1946-02-13 1949-10-18 American Cyanamid Co Preparation of acrylic acid and esters thereof
US2559878A (en) * 1948-12-29 1951-07-10 Western Electric Co Zinc and cadmium passivating bath
US3343930A (en) * 1964-07-14 1967-09-26 Bethlehem Steel Corp Ferrous metal article coated with an aluminum zinc alloy
US3393089A (en) * 1964-07-14 1968-07-16 Bethlehem Steel Corp Method of forming improved zinc-aluminum coating on ferrous surfaces
US3619441A (en) * 1969-04-03 1971-11-09 Southern Block And Pipe Corp Metal treatment to prevent corrosion and blemishes in metal reinforced concrete structures
US3952120A (en) * 1974-05-31 1976-04-20 Bethlehem Steel Corporation Aluminum-zinc coated low-alloy ferrous product and method
US4023600A (en) * 1974-10-10 1977-05-17 Firma Evg Entwicklungs-U Verwertungsgesellschaft Method of producing wire mesh
US4171231A (en) * 1978-04-27 1979-10-16 R. O. Hull & Company, Inc. Coating solutions of trivalent chromium for coating zinc surfaces
US4287008A (en) * 1979-11-08 1981-09-01 Bethlehem Steel Corporation Method of improving the ductility of the coating of an aluminum-zinc alloy coated ferrous product
US4359348A (en) * 1981-06-17 1982-11-16 Occidental Chemical Corporation Stabilized trivalent chromium passivate composition and process
US4448748A (en) * 1980-03-25 1984-05-15 International Lead Zinc Research Organization, Inc. Zinc-aluminum alloys and coatings
US4605598A (en) * 1983-06-28 1986-08-12 Fils Et Cables D'acier De Lens (Fical) Steel wire having superposed coatings resisting corrosion
US4774825A (en) * 1984-12-10 1988-10-04 N.V. Bekaert S.A. Method for cladding a wire-shaped steel element with an aluminum coating, as well as aluminum-coated wire-shaped steel element
US4776898A (en) * 1985-03-20 1988-10-11 Omi International Corporation Passivation
US4931317A (en) * 1988-03-30 1990-06-05 Nihon Parkerizing Co., Ltd. Composition and process for the formation of a black coating on surfaces of materials
US4966634A (en) * 1986-07-14 1990-10-30 Nihon Parkerizing Co., Ltd. Composition of the surface treatment for metal and the treatment method
US5096666A (en) * 1988-09-02 1992-03-17 Farnsworth Verdun H Rare earth and aluminium containing galvanizing bath and method
US5219617A (en) * 1989-09-19 1993-06-15 Michigan Chrome And Chemical Company Corrosion resistant coated articles and process for making same
US5236574A (en) * 1989-05-08 1993-08-17 Sumitomo Metal Industries, Ltd. Electroplating of hot-galvanized steel sheet and continuous plating line therefor
US5330588A (en) * 1993-02-02 1994-07-19 E2Ki & Associates Inc. Organic-aqueous composition and process for forming corrosion-resistant coatings on metal surfaces
US5368655A (en) * 1992-10-23 1994-11-29 Alchem Corp. Process for chromating surfaces of zinc, cadmium and alloys thereof
US5393354A (en) * 1993-10-07 1995-02-28 Mcgean-Rohco, Inc. Iridescent chromium coatings and method
US5415702A (en) * 1993-09-02 1995-05-16 Mcgean-Rohco, Inc. Black chromium-containing conversion coatings on zinc-nickel and zinc-iron alloys
US5876517A (en) * 1994-12-07 1999-03-02 Atotech Deutschland Gmbh Chromate-plating bath and process for finishing zinc zinc alloy or cadmium surfaces
US20010008654A1 (en) * 1997-01-02 2001-07-19 Manuel B. Ferrero Zinc alloys yielding anticorrosive coatings on ferrous materials
US6305432B1 (en) * 2000-06-19 2001-10-23 Sacks Industrial Corp. Wire mesh having flattened strands
US6858098B2 (en) * 2001-11-30 2005-02-22 Dipsol Chemicals Co., Ltd. Processing solution for forming hexavalent chromium free and corrosion resistant conversion film on zinc or zinc alloy plating layers, hexavalent chromium free and corrosion resistant conversion film, method for forming the same

Patent Citations (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2035380A (en) * 1933-05-13 1936-03-24 New Jersey Zinc Co Method of coating zinc or cadmium base metals
US2276353A (en) * 1935-09-28 1942-03-17 Parker Rust Proof Co Process of coating
US2250508A (en) * 1936-06-15 1941-07-29 John S Thompson Treating zinc with organic acids
US2327002A (en) * 1939-03-09 1943-08-17 Parker Rust Proof Co Coated article and method of making the same
US2393640A (en) * 1944-11-11 1946-01-29 Rheem Res Products Inc Dyed metals
US2485510A (en) * 1946-02-13 1949-10-18 American Cyanamid Co Preparation of acrylic acid and esters thereof
US2559878A (en) * 1948-12-29 1951-07-10 Western Electric Co Zinc and cadmium passivating bath
US3393089A (en) * 1964-07-14 1968-07-16 Bethlehem Steel Corp Method of forming improved zinc-aluminum coating on ferrous surfaces
US3343930A (en) * 1964-07-14 1967-09-26 Bethlehem Steel Corp Ferrous metal article coated with an aluminum zinc alloy
US3619441A (en) * 1969-04-03 1971-11-09 Southern Block And Pipe Corp Metal treatment to prevent corrosion and blemishes in metal reinforced concrete structures
US3952120A (en) * 1974-05-31 1976-04-20 Bethlehem Steel Corporation Aluminum-zinc coated low-alloy ferrous product and method
US4023600A (en) * 1974-10-10 1977-05-17 Firma Evg Entwicklungs-U Verwertungsgesellschaft Method of producing wire mesh
US4171231A (en) * 1978-04-27 1979-10-16 R. O. Hull & Company, Inc. Coating solutions of trivalent chromium for coating zinc surfaces
US4287008A (en) * 1979-11-08 1981-09-01 Bethlehem Steel Corporation Method of improving the ductility of the coating of an aluminum-zinc alloy coated ferrous product
US4448748A (en) * 1980-03-25 1984-05-15 International Lead Zinc Research Organization, Inc. Zinc-aluminum alloys and coatings
US4359348A (en) * 1981-06-17 1982-11-16 Occidental Chemical Corporation Stabilized trivalent chromium passivate composition and process
US4605598A (en) * 1983-06-28 1986-08-12 Fils Et Cables D'acier De Lens (Fical) Steel wire having superposed coatings resisting corrosion
US4774825A (en) * 1984-12-10 1988-10-04 N.V. Bekaert S.A. Method for cladding a wire-shaped steel element with an aluminum coating, as well as aluminum-coated wire-shaped steel element
US4776898A (en) * 1985-03-20 1988-10-11 Omi International Corporation Passivation
US4966634A (en) * 1986-07-14 1990-10-30 Nihon Parkerizing Co., Ltd. Composition of the surface treatment for metal and the treatment method
US4931317A (en) * 1988-03-30 1990-06-05 Nihon Parkerizing Co., Ltd. Composition and process for the formation of a black coating on surfaces of materials
US5096666A (en) * 1988-09-02 1992-03-17 Farnsworth Verdun H Rare earth and aluminium containing galvanizing bath and method
US5236574A (en) * 1989-05-08 1993-08-17 Sumitomo Metal Industries, Ltd. Electroplating of hot-galvanized steel sheet and continuous plating line therefor
US5219617A (en) * 1989-09-19 1993-06-15 Michigan Chrome And Chemical Company Corrosion resistant coated articles and process for making same
US5368655A (en) * 1992-10-23 1994-11-29 Alchem Corp. Process for chromating surfaces of zinc, cadmium and alloys thereof
US5330588A (en) * 1993-02-02 1994-07-19 E2Ki & Associates Inc. Organic-aqueous composition and process for forming corrosion-resistant coatings on metal surfaces
US5415702A (en) * 1993-09-02 1995-05-16 Mcgean-Rohco, Inc. Black chromium-containing conversion coatings on zinc-nickel and zinc-iron alloys
US5393354A (en) * 1993-10-07 1995-02-28 Mcgean-Rohco, Inc. Iridescent chromium coatings and method
US5876517A (en) * 1994-12-07 1999-03-02 Atotech Deutschland Gmbh Chromate-plating bath and process for finishing zinc zinc alloy or cadmium surfaces
US20010008654A1 (en) * 1997-01-02 2001-07-19 Manuel B. Ferrero Zinc alloys yielding anticorrosive coatings on ferrous materials
US6305432B1 (en) * 2000-06-19 2001-10-23 Sacks Industrial Corp. Wire mesh having flattened strands
US6858098B2 (en) * 2001-11-30 2005-02-22 Dipsol Chemicals Co., Ltd. Processing solution for forming hexavalent chromium free and corrosion resistant conversion film on zinc or zinc alloy plating layers, hexavalent chromium free and corrosion resistant conversion film, method for forming the same

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102996975A (en) * 2012-12-17 2013-03-27 济南玫德铸造有限公司 Pipe fitting with double galvanized layers and manufacturing method thereof
TWI480538B (en) * 2013-05-21 2015-04-11 China Steel Corp Method of optically determining metallography of iron-zinc galvannealed intermetallic layer
US20150298158A1 (en) * 2014-04-22 2015-10-22 Metokote Corporation Zinc rich coating process
US9956576B2 (en) * 2014-04-22 2018-05-01 Metokote Corporation Zinc rich coating process
US10717104B2 (en) 2014-04-22 2020-07-21 Metokote Corporation Zinc rich coating process
WO2019001872A1 (en) * 2017-06-29 2019-01-03 Nv Bekaert Sa Pre-stressed concrete structure with galvanized reinforcement
US10753095B2 (en) 2017-06-29 2020-08-25 Nv Bekaert Sa Pre-stressed concrete structure with galvanized reinforcement

Similar Documents

Publication Publication Date Title
JP5112422B2 (en) Method for producing a flat steel product coated by a corrosion protection system
US5114799A (en) Material for roofing and facing
US20070119715A1 (en) Corrosion Resistant Wire Products and Method of Making Same
JP2005169765A (en) Coated zn-al alloy plated steel sheet excellent in corrosion resistance
AU2021365696A1 (en) Plated steel material
US6372296B2 (en) High aluminum galvanized steel
Lynch Hot-dip galvanizing alloys
JP2004323932A (en) Coated steel sheet, base material plated steel sheet thereof and their production methods
JP4312635B2 (en) Painted aluminized steel sheet with excellent corrosion resistance
Shimoda et al. Corrosion resistance of several Zn-Al-Mg alloy coated steels
KR102639488B1 (en) plated steel
AU4348199A (en) Method of galvanizing with molten zinc-aluminum alloy
JP2002080952A (en) Home building material excellent in corrosion resistance, and home building member
JPS63143269A (en) Production of alloy plated steel products having excellent corrosion resistance and workability
US4548872A (en) Protection process of flat rolled steel sections by means of multi-layer electrolytic plating in particularly aggressive environments
JP2004232029A (en) COATED HOT DIP Al-Zn BASED ALLOY PLATED STEEL SHEET HAVING EXCELLENT SURFACE APPEARANCE, AND PRODUCTION METHOD THEREFOR
JPS63134653A (en) Manufacture of alloy-plated steel material excellent in corrosion resistance and workability
JPH09143659A (en) Galvannealed steel sheet excellent in initial white rust resistance
Zhang et al. Properties, Products, and Processes
JP2825724B2 (en) Striped steel sheet with excellent workability and corrosion resistance
JP2982653B2 (en) High corrosion resistance Al-Zn alloy hot-dip coated steel sheet and manufacturing method thereof
US20140190229A1 (en) Method for improving light gauge building materials
CN107058931A (en) A kind of production method of color painted steel strip or steel band
Leonard Precoated steel sheet
Dallin Control and treatment of hot-dip galvanized surfaces

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION