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Issues Impacting Bridge Painting: an Overview
FHWA/RD/94/098 –August 1995

Abstract | Table of Contents | Executive Summary | Chapter 1 | Chapter 2 | Chapter 3 | Chapter 4 | Chapter 5 | Chapter 6 | Chapter 7 | Appendix A | References | List of Figures | List of Tables

Chapter 5. Task D - Advanced Coatings

Table of Contents

INTRODUCTION

The rehabilitation of steel structures, in general, and bridges, in particular, is a significant drain on resources, including manpower and budget. As restrictions on both the permissible methods of paint removal and the VOC content of paint systems increase, the options available to bridge owners diminish.

For years, standard maintenance painting practice for steel bridges has entailed the use of open-abrasive blasting for the complete removal of existing paint prior to repainting. Open-abrasive blasting not only removes the existing paint, but also cleans the steel surface of corrosion products and millscale while providing a roughened surface profile desirable for the adhesion of new paint. In the past, lead-containing paint provided a reliable economical solution to the long-term corrosion protection of these structures without requiring extensive surface preparation such as the removal of millscale. Recent concerns over the effects of lead as a toxic substance in the environment and the release of VOCs during the application of paints has caused a radical change of direction to be pursued in the painting of steel highway bridges. The primary objective of task D was to investigate advanced coatings that have the potential to meet the changing needs associated with the rehabilitation of steel bridges.

BACKGROUND

Organic coatings are applied onto steel surfaces to provide a barrier to minimize the interaction of the steel and corrosive elements of the environment. In order to be successful, these coatings must delay and limit ingress of the aggressive corrosive elements: water, oxygen, and ionic species such as Cl- and SO4=. These aggressive corrosive elements can reach the substrate/coating interface either by intrusion through defects or by diffusion through the protective coating. While the incidence of defects can be reduced by proper coating application based on good quality control practices, the diffusion of oxygen and salts in solution will always take place. However, the rate of diffusion varies widely, based on the coating system chosen. Considerable research has been performed on the mechanism of coating degradation. However, due to the complexity of metal/coating and coating/environment systems, theories do not exist that quantitatively or even qualitatively describe the coating degradation processes and relate them in a manner that allows the prediction of the performance of coating systems during service. FIGURE 52 describes one model, developed by NIST, indicating the major factors that they perceive as influencing the durability of a coating system.

Aging is one of the factors that affect coating durability and is a direct measure of the success or failure of the system to provide its stated goal of protecting the substrate. It is primarily aging that determines when, and to what degree, a coating system is removed and replaced.

As mentioned in task A, advanced coatings can benefit the maintenance of steel bridges within the following options: (1) Total paint removal and recoating, and (2) Partial paint removal and overcoating.

In addition, advanced coatings can be of benefit during the rehabilitation of steel bridges that require replacement of structural components.

Total paint removal and replacement may be the best economical option if more than 20 percent of its protective coating system has failed. Within the context of total paint removal, several options exist which are based on the integrity of the structural elements. If component replacement is not necessary and/or can be deferred, a VOC-compliant paint system with an expected lifetime comparable to the next planned rehabilitation of the structure can be chosen.

If component replacement is necessary, a coating system applied in the fabrication shop should be chosen such that it can both perform and be repaired in the field. However, fabrication shops have to face increasing challenges in this area, again due to the implementation of ever more stringent VOC requirements as discussed below.

DILEMMAS FACING FABRICATION SHOPS

Increased Shop Painting

For many years, highway agencies specified paint systems for new bridges that were reasonably long-lasting and relatively simple for steel fabrication shops to apply. Initially, shop painting involved the application of a primer coat that was supplemented by additional coat(s) of paint applied after the steel was shipped to a job site and erected. Multi-coat paint systems offering enhanced performance have gradually been adopted by many highway agencies, resulting in a desire to limit or eliminate field painting. This is partially due to the increased control of the painting and quality control practices in a shop environment. At least eight highway agencies have adopted the practice of complete shop painting, limiting field painting to touch up work.

Containment For Maintenance Painting

Environmental regulations currently prohibit environmental releases of particulates generated by abrasive blasting during maintenance painting of bridges in urban areas. Worker exposure to these particulates necessitates the use of protective respirators, even when abrasive blasting operations do not involve lead-based paints. In the future, it is likely that all bridge maintenance painting incorporating abrasive blasting will require total containment. Highway agencies anticipating that eventuality are currently seeking extremely durable shop coatings to forestall the need for maintenance painting.

Fabrication Shop Problems

In the past, fabrication shop personnel considered shop painting as a nuisance, however, it was necessary to sell fabricated steel. In many cases, the quality of painting operations in those shops took a back seat to other activities such as welding. The forgiving nature of the early oil-alkyd paints promoted that antipathy. The advent of advanced structural steel paints, such as the inorganic zinc/vinyl systems demonstrated the need for improved quality control. For example, poor control of wet thickness for inorganic zinc paints resulted in "mud cracking." As more highway agencies have required the shops to perform more painting work using high-performance paint systems, painting has had greater impact on shop profitability and the quality of shop painting has became more critical.

Regulation of Fabrication Shops

Fabrication shops are point sources of waste generation. As a result, they are easy targets for regulation by State departments of environmental protection (DEP's). Those agencies promulgated regulations restricting the VOC content in paints. In addition, if materials are used that exceed these limits, the fabrication shops are faced with a limit on their total yearly VOC emissions. Highway agencies specifying paints with high-VOC content have been forced to employ lower VOC coatings or the fabrication shops nearing their VOC point-source limits are unable to supply the components.

Current limitations on VOC content of paints and the total allowed yearly VOC emissions by fabrication shops will most likely be tightened in the future. The VOC regulations for paints, as the result of the ongoing regulation-negotiation activities related to architectural industrial maintenance will most likely reduce the VOC limits on bridge maintenance paints to 336 g/L (2.8 lbs/gal). Most states require for new construction that point sources use paints with a VOC limit of 420 g/L (3.5 lbs/gal). In States restricting the total yearly VOC emissions from fabrication shops, those restrictions probably will be more limiting than that for the VOC content.

A solution to the problems of both highway agencies and fabrication shops would be for State highway agencies to specify water-based paint systems such as the acrylic systems now offered by a number of paint companies. However, while these systems may meet present and projected VOC restrictions, they are not as durable, particularly in high-salt environments, as conventional solvent-based systems. In addition, waterborne paints are less application-tolerant than their solvent-based counterparts. They require close control of application conditions (e.g., temperature and humidity) and surface cleanliness (e.g., sensitivity to surface oils and other contamination). Fabrication shops able to apply high-performance solvent-based paints have experienced problems with waterborne systems. Due to shop layouts and the proximity to other operations, some of those problems are difficult to resolve and severely limit painting operations when waterborne systems are employed. Several highway agencies have experienced reduced performance using those systems on new bridges.

Many polymer manufacturers and paint companies have invested heavily in water-based paint technology. With continued research, some of the problems currently experienced with waterborne systems will be remedied over the next 5 to 10 years. However, it is problematical that coating durability of waterborne paints will improve sufficiently to match that of some of the solvent-based systems presently in use, such as inorganic zinc.

The 100-hundred percent solids paint technology employs two-component systems that react chemically and polymerize to form a solid film. The coatings are automatically mixed during the feeding process or internally mixed in the spray-gun head during application. Common two-component systems include epoxies, polyureas, and polyurethanes. The 100-hundred percent solids painting generates no VOC's. Typically, onethe 100-percent solids paints are applied in high builds 0.5 to 0.75 mm (20 to 30 mils). The coating components react and dry quickly (typically within 15 to 30 min), facilitating shop handling. Special application and handling equipment, coating materials, and operator training are required. Coating costs will initially be somewhat higher than for conventional solvent-based paint systems. These costs are anticipated to be offset by somewhat longer service lives. The 100-hundred percent solids paints are presently being employed on chemical plants, boat hulls, and railway cars.

The Union Carbide Corporation has developed a proprietary paint application method, the Unicarb System, that uses carbon dioxide to replace up to 80 percent of the solvents in conventional solvent-based paint systems. Carbon dioxide gas is introduced in a spray gun during application. It improves paint atomization during spraying and acts as a carrier for the paint. The method has the advantage of being able to employ current solvent-based paint technology, while achieving a significantly reduced VOC release level. The reduced level of VOC's causes the paint to dry fairly rapidly (depending on the paint system), facilitating handling. Special application equipment, coating materials (i.e., compressed gas-carbon dioxide), and operator training are required. Coating costs will initially be slightly higher than for conventional solvent-based systems. The same coatings applied using the Unicarb System in place of conventional solvents have had relatively lower permeability. Therefore, longer service lives may be obtained. The Unicarb System has been employed for commercial products; it has been demonstrated successfully in several areas, including automotive and aircraft applications. The system as presently employed appears to be more economically attractive for higher production rate, repetitive operations.

OVERCOATING

Spot repair and overcoating of compromised coatings involves: (1) cleaning the surface of the bridge with pressurized water to remove salts, soils, and other contaminants, (2) mechanically removing loose corrosion products and paint, (3) spot priming areas where paint and corrosion products have been removed, and (4) applying coats of paint over the entire surface. The conditions required for successful overcoat application are: (1) adequate adhesion and mechanical properties of the old paint, (2) compatibility of the overcoat system to existing coating system, and (3) proper surface preparation. In the past, many highway agencies maintained bridge paint systems by overcoating. Typically, existing lead-based alkyd systems were overcoated with similar or identical paints that provided years of acceptable service. Maintained alkyd paint systems have lasted well over 15 years. Often, oil-alkyd painted bridges were overcoated until they had paint builds as high as 0.75 to 1.0 mm (30-40 mils).

Overcoating has some potential advantages compared to full removal with containment. It minimizes the disturbance of the existing paint, which in turn, limits the generation of (possibly hazardous) wastes and minimizes precautions necessary for preventing waste discharge, worker exposure to lead, and efforts required to dispose of generated wastes. Repair and overcoating operations do not require expensive containment enclosures. Costs for repair and overcoating are low (typically one-fifth to one-third that for full removal with containment) and overcoating. Overcoating may extend the service life of the in-place coating system by 15 years or more. Low initial painting costs coupled with potentially significant extension of service life are very attractive to State highway agencies strapped with limited painting budgets and large backlogs of bridges needing to be repainted. However, there exists significant danger of short-term failure of the complete system if the original coating system does not have sufficient adhesion/mechanical properties or if a non-compatible repair system is chosen.

The uncertainty with this maintenance option is that long-term experience with many of the newer paint systems as repair material is lacking.

Factors Affecting Performance and Durability of Overcoating Systems

In the following section, we will discuss the factors that affect the success or failure of an overcoating job. The relative importance of the discussed factors is not clearly understood. Furthermore, in many cases, the current test methods available do not clearly characterize various factors.

Adhesion/cohesion

The use of adhesion tests to rate the ability of an existing paint system to be overcoated and to estimate the durability/compatibility of the repair merit review. Current tests are time-consuming to perform, difficult to repeat, and the meaning of the results are subject to individual interpretation. For example, large differences have been observed between the test results when different methods are used. Existing paints may be brittle and lack cohesion and intercoat adhesive strength (i.e., typically occurring between an alkyd primer and existing intermediate or topcoats of alkyd paints containing aluminum pigments). Knifing adhesion tests such as ASTM D3359-90 (Measuring Adhesion by Tape Test) typically fracture old alkyd paints causing intercoat (cohesive) failure. The pull-off test, ASTM D-4541 (Standard test Method for Pull-Off Strength of Coatings Using Portable Adhesion Testers), measures adhesion between existing coats or between the primer and the substrate, or the cohesive strength of a specific coat depending upon which component fails first. Brittle alkyds may provide only a 1B or 0B rating using the knifing adhesion test. If used on existing paint that contains several overcoated layers, the knifing adhesion test may provide similar values. However, a pull-off adhesion test on the same system may provide readings in excess of 2067 kPa (300 lb/in2).

Surface Contamination

The presence of soluble salts on existing paint surfaces and in corrosion products pose a distinct threat to repair coating's durability. Soluble salts must be removed in order to provide extended paint durability even though their effects are difficult to assess. They are difficult to detect in the field and their concentration may vary depending on level of deicing salt application, bridge design, and structural location. Currently, the primary tests for chloride surface contamination are wet chemical tests that are slow to perform and are questionable as to accuracy and precision.

THERMAL SPRAY TECHNOLOGY

Introduction

As can be seen, the dilemmas facing facility owners and fabrication shops are complex. One potential answer may be thermal spray (TS) technology. TS is a coating process that has been proven in FHWA, National Association of Corrosion Engineers (NACE), U.S. Navy (USN), and other sponsored programs to provide superior long term corrosion protection in a variety of environments. As part of task D, Thermal Spray was evaluated by both ongoing field tests and also as part of task E, Accelerated Testing.

Thermal Spray Coatings

The term "thermal spray" is commonly used to describe a family of coating technologies associated with the application of thick coatings onto components in order to reduce or eliminate the debilitating effects of wear and corrosion. In general, material in either powder, wire, or rod form is introduced into a region of high enthalpy (FIGURE 53). Within this region, the material is brought to either a plastic or molten state. As part of this process, an expanding gas is used to accelerate the droplets onto the component surface, forming a coating. As the droplets impact onto the surface, they form lenticular splats (FIGURE 54) and form a coating layer. The coating is built up to the desired thickness by multiple passes over the component surface. As with any coating, the surface must be properly prepared in order to insure coating adherence. In the case of thermal spray coatings applied in open atmosphere, the proper surface preparation is the roughening of the surface either by grit blasting or chemical etching in order to generate the asperities necessary for the mechanical bonding of the coating to the component surface. In addition, thermal spraying is a line-of-sight process with optimum coatings being obtained when the angle of impingement of the molten droplets is perpendicular to the surface being coated. Depending on the process being used, excellent coatings can be obtained when the droplets impinge at angles between 90 and 45o relative to the surface being coated. Below 45o, evaluation of the coating microstructure determines the applicability of a given coating and process to the problem being addressed.

Flame spraying, the oldest form of thermal spraying, has been used since the late 1800's. In its simplest form, it consists of a nozzle assembly wherein a fuel (acetylene, hydrogen, propane, etc.) is mixed either with oxygen or air and undergoes combustion external to the nozzle. The flame front is stabilized by matching the flame propagation speed to the average unburned gas velocity. Heat transferred to the nozzle also aids in anchoring the flame front. For materials in powder form (FIGURE 55a), the powder is injected into the flame in a manner designed to optimize the heating of the powder. For materials in wire or rod form (FIGURE 55b), the flame is concentric to the wire or rod in order to maximize the uniform heating of the wire rod. A coaxial sheath of compressed gasses around the flame acts to atomize the molten particles and accelerate them toward the substrate. The main advantages of these processes are low capital investment costs and ease of operation. Because of the relatively small size of the equipment and the ease of operation, the process is field-portable, and there is little restriction to the size and complexity of components that can be coated. However, particle velocities are relatively low and, therefore, the coating porosity can be as high as 20 percent.

The electric arc process is illustrated in FIGURE 55c and involves the continuous feeding of two wires into a device such that the wires converge at a point in space. The wires are held at different electrical potentials, such that an electric arc is generated between them. These wires are, in essence, consumable electrodes and are continuously melted. A jet of gas, usually compressed air, is used to atomize the molten material and accelerate the resultant droplets onto the component surface. It is not necessary for both wires to have the same chemical composition resulting in alloyed coating, however, adjustments to the feeding mechanism are necessary to compensate for these differences. Very high deposition rates are achievable by this process, but the atomization process generates more fumes than other thermal spray processes. In addition, this process frequently results in porosity levels of 25 percent by volume. Recent advances in the design of electric arc equipment have incorporated the use of Coanda accelerators. The Coanda accelerators use the geometry of the flow chamber to enhance the syphoning action of the atomizing gas, thereby increasing the volumetric flow through the same cross-sectional flow area. This results in higher particle velocities and coatings of higher density.

Thermal Spray Materials

As with any coating process, the proper choice of coating materials may determine whether or not the desired goals are achieved. Historically, thermal spray coating systems have used pure zinc, pure aluminum, and zinc/aluminum alloys for applications involving corrosion protection of steel structures. Being metallic, the coatings offer additional protection in high-wear areas.

Zinc

Zinc provides long-term corrosion protection to steel through galvanic action at the zinc/steel surface as well as by its ability to protect itself with its own corrosion byproducts. Zinc has a lower oxidation potential than iron and will therefore preferentially corrode, preventing the steel from rusting. In addition, this properly provides cathodic protection to any small discontinuities or damage done to the zinc coating that may expose the steel components. Being a reactive metal, zinc readily forms a protective corrosion-product film. When exposed to air, a very thin layer of zinc oxide forms. When exposed to moisture in the atmosphere, the zinc oxide reacts with the moisture to form zinc hydroxide. During the drying process, the zinc hydroxide reacts with carbon dioxide to form an insoluble zinc carbonate layer on the surface, providing excellent protection to the underlying zinc.

Aluminum

Aluminum provides a barrier to the corrosion of steel by the formation of an inert aluminum oxide layer on the surface of the coating. When damaged, this coating is self-healing. Like zinc, aluminum has a lower oxidation potential than steel with respect to iron and therefore provides galvanic protection to the steel substrate. Unlike zinc, pure aluminum has not been extensively thermally sprayed onto steel bridges and structures although extensive use by the U.S. Navy indicates aluminum is more corrosion-resistant than zinc in marine environments. FIGURE 56 describes the estimated service life for aluminum thermal spray coatings.

Zinc/Aluminum

With the proven protection associated with zinc and the implied improved performance of aluminum in salt environments, alloys of zinc and aluminum have been developed. Initial work in Japan indicates that such alloys, particularly 85 percent zinc/15 percent aluminum alloy, have advantages over all-zinc coatings. This alloy has successfully been applied to steel bridges within the United States. FIGURE 57 describes the estimated service life for Zn and 85/15 Zn/Al thermal spray coatings.

Recently, the application of polymers such as ethylene acrylic acid EAA) by thermal spray technology[A has been suggested for corrosion prevention on bridges. Unfortunately, unlike the metallic coatings described above, success has been limited for two reasons. First, control of the substrate temperature is critical for adhesion and to date no definitive method for insuring the proper temperature has been proposed. Second, like most paint systems, these coatings are solely barrier coatings without any additional protective mechanisms such as those exhibited by the metallic coatings.

Sealers

Although zinc, aluminum, and their alloys provide galvanic protection, additional protection can be obtained by sealing the porosity with acrylic urethanes, polyester urethanes, vinyls, phenolics, epoxy sealers, or thermally sprayed polymers.

INFRASTRUCTURAL APPLICATIONS OF THERMAL SPRAY TECHNOLOGY

There is a history of corrosion protection by aluminum and zinc thermal spray coatings for structural steel work: buildings, bridges, towers, radio and TV antenna masts, steel gantry structures, high-power search radar aerials, overhead walkways, railroad overhead line support columns, electrification masts, tower cranes, traffic-island posts, and street and bridge railings.

The interior of steel-hopper rail cars for hauling coal have been sprayed with aluminum for sulfuric acid corrosion protection and with aluminum composite for both corrosion and abrasion protection. Steel car exteriors have been sprayed with zinc for atmospheric- corrosion protection.

Zinc thermal spray coatings used to protect potable water pipelines and storage tanks as specified in ANSI/AWWA D-102-78, American Water Works Association Standard for Painting Water-Storage Tanks. (5). Aluminum and zinc thermal spray coatings are used on sluice gates in irrigation systems and canal lock gates in shipping canals. These coated components have required virtually no maintenance for decades.

In marine applications, ship structural areas and components are preserved with aluminum and zinc thermal spray coatings. The U.S. Navy routinely uses aluminum thermal spray coatings in new ship construction and in the overhaul, repair, and maintenance of ship structures and for a wide range of shipboard components, especially those in topside and wet spaces. The British, Australian, and New Zealand Navies use a duplex zinc (base) and aluminum (top) thermal spray coatings system.

Zinc thermal spray coatings complement hot-dip galvanizing when fabrications are excessively large or otherwise cannot be hot-dip galvanized. Zinc thermal spray coatings are used for repairing galvanized coating damaged during the fabrication process (e.g., welding, cutting and joining areas) and for maintenance recoating. Here, zinc spray is particularly advantageous because it ensures the uniformity and reproducibility of the galvanized coating thickness.

THERMAL SPRAYING OF STEEL BRIDGES: A SHORT HISTORY

Thermal spraying of bridges is not a new idea. Since the 1930s, zinc spraying has been extensively utilized in Europe, and in many countries zinc spraying is specified as the only corrosion protection system for new bridge construction. To date, several hundred bridges have been thermally sprayed to provide long-term corrosion protection. TABLE 8 lists several significant bridges, the year of metallization, and the last date when the coatings were inspected and found to be intact. In the United States, the oldest known bridge to be thermally sprayed is the Kaw River Bridge in Kansas City, Missouri. In 1936, the bridge was sprayed with between 0.25 to 0.30 mm (10 to 12 mils of pure zinc. The bridge with the most notoriety is the Ridge Avenue bridge in Philadelphia, the underside of which was sprayed with 00.25 mm (10 mils) of pure zinc in 1937. The Ridge Avenue Bridge is a railroad overpass and therefore has been subjected to severe corrosion environments due both to its exposure to the effluence of generations of steam and diesel locomotives as well as to road salts. Fifty-five years later, the zinc coating is still effectively protecting the bridge. The Forth Road Bridge in the United Kingdom is noteworthy in that it is the largest structure in the world to have its entire outer surface thermally sprayed. In 1961, over 18,140 Mg (20,000 tons) of structural steel was metallized with a 0.125-mm (5-mil) coating of zinc, and upon assembly, supplemented with three coats of paint. The Pierre-LaPorte Bridge spanning the St. Lawrence River near Quebec City, Canada, is the largest onsite metallized structure in the world. The original construction of the bridge was completed in 1970. The corrosion protection system consisted of painting with a lead silico-chromate, oil, and alkyd system. Maintenance and repainting of the bridge began in 1975. In 1977, the Province of Quebec decided to zinc spray the entire understructure of the bridge [160,000 m2 (1.8 million ft2)]. An economic study concluded that while the paint system would have provided an 8-year lifespan requiring frequent touchups, the alternate zinc spray system would give a probable life of 20-25 years, requiring no major touchups. As recently as 1991, the coating was providing superior corrosion resistance on the bridge.

Since 1985, Ohio has coated four bridges with the thermal spray process. The first bridge selected consisted of five lines of 21 WF 62s, 32 m (102 ft) long, over a stream. The surface area of steel to be coated was 309 m2 (3323 ft). The bridge was to have a new concrete bridge deck constructed on the existing beams. The metallizing of the beams was to be done after the deck was replaced. The beams were required to be sandblasted to a white metal surface (SP 5) and the 85 percent zinc/15 percent aluminum metallizing was to be applied [0.15-2.0 mm (6-8 mils) thick] followed by 0.0375 mm (1.5 mils) of epoxy, and 0.05 mm (2 mils) of a urethane topcoat. The metallizing had to be applied within 4 h of sandblasting to avoid flash rusting of the freshly blasted surfaces. The bid price on this first bridge for surface preparation, metallizing, epoxy intermediate coat, and urethane topcoat was $30,000 or $95.35/m2 ($9.03/ft2). This cost did not include containment of blasting debris since this work was done before containment was a requirement in Ohio. The actual time required for metallizing the beams was 8 working days. To date, this bridge remains in excellent condition and exhibits no rusting of the steel beams.

A second bridge was selected to be metallized in 1985. This structure was considerably more complicated to metallize because: (1) it is a bridge over an Interstate highway and (2) the beams are composed of riveted plates and angles. The bridge consisted of four lines of riveted beams each being 111 m (364 ft) long. Again, this was to have a concrete deck replacement with the metallizing to be done after the deck had been replaced. Containment of the blasting debris was not a requirement on this project. The bid price for cleaning and painting this bridge was $217,000 or $87.44/m2 ($8.28/ft2).

In an effort to better evaluate the effectiveness of the metallizing, it was decided not to topcoat the beams with the epoxy and urethane, but rather only seal the metallized surface with a clear sealer. This bridge, being situated over an Interstate highway, is subject to much salt spray and to date, the beams remain in excellent condition.

At the time of metallizing these two bridges, standard paint systems were costing $36.96/m2 ($3.50/ft2) and it seemed unlikely at that time that metallizing would ever become cost-competitive on a first-cost basis. However, recent cost increases in standard systems are narrowing the margin between metallizing and conventional painting.

A third bridge, which carries a local road over a four-lane divided highway, was selected for metallizing in 1988. This bridge was also to receive a reinforced concrete deck replacement with the metallizing of the steel beams to be completed after the deck was replaced. The bid price for metallizing the four lines of 30 WF steel beams, 117.2 m (384.5 ft) long, was $237,000 or $91.66/m2 ($8.68/ft2). This price included surface preparation, but not full containment (which was still not required at that time).

TEST PANEL PREPARATION

As part of this task, 210 test panels were prepared for field and accelerated testing. Initially, it was proposed that in addition to thermally sprayed test panels, paint systems under testing at the Mathis River Bridge in New Jersey would be included in testing. This was proposed to provide a baseline comparison between the paint coating systems and the thermally sprayed coating systems. Unfortunately, many of the paint systems tested at Mathis River are no longer VOC-compliant and, therefore, it was decided that paint systems meeting existing and proposed VOC limits would be used in this study. TABLE 9 details the thermally sprayed samples prepared and TABLES 10a and 10b detail the paint systems samples prepared.

All coatings were applied onto standard 102-mm by 152-mm by 4.76-mm (4-in by 6-in by 3/16-in) A-36 steel panels purchased from KTA Tator. All samples were degreased in a vapor degreaser/ultrasonic bath containing 1,1,1 trichloromethane. They were then grit-blasted using 36 grit aluminum oxide at 511 kPa (80 lb/in2) to a SP-5 white metal finish with at least a 0.051-mm (0.002-in) profile as shown in FIGURE 58. Using ANSI/AWS C2.18-93, Guide for the Protection of Steel with Thermally Sprayed Coatings of Aluminum, Zinc, and their Alloys and Composites, the zinc (FIGURE 59), aluminum (FIGURE 60), and the 85/15 zinc/aluminum (FIGURE 61) samples were prepared. The EAA coating (FIGURE 62) was applied using manufacturer supplied parameters. In addition, the paint systems were applied following manufacturers' guidelines.

A typical set of samples for field testing was composed of one each of paint systems 1 through 5 and one each of the thermally sprayed zinc, aluminum, and 85/15 zinc/aluminum. In addition, one each of the zinc, aluminum, and 85/15 zinc/aluminum test samples had one-half of each panel sealed with the cycloaliphatic/aliphatic amine epoxy. Finally, one each of the 85/15 zinc/aluminum test samples had one-half of each panel thermally sprayed with the EAA copolymer. One set of test panels has been deployed to the I-55 bridge with three remaining sets to be deployed in early 1994. Follow-on evaluation of these panels will occur as part of an ongoing 4-year program on overcoating. The remaining samples were supplied for evaluation under task E.

CONCLUSIONS AND RECOMMENDATIONS

The most critical factor in the implementation of advanced coatings is the relative lack of history as it pertains to the durability of these coatings with the exception being thermally sprayed coatings. One difficulty with the implementation of thermally sprayed coatings is the relative age of the infrastructure and limited access to portions of the bridges where advanced corrosion has occurred.

Since many bridges have suffered loss of cross section, the application of thermally sprayed coatings retard corrosion, but cannot replace lost steel. In addition, since the regions of most serious corrosion are in the area of expansion joints and bearing areas, thermal spray technology's need for line of sight can limit the quality of coating applied. This should not preclude use of this technology when the above-mentioned limitations do not contraindicate its use.

Two immediate areas where thermal spray technology can be implemented are in structural replacement and fabrication. In these applications, if the steel at an expansion joint was sprayed with 85/15 Zn/Al it would provide long-term corrosion protection and minimize loss of cross section.

The use of paint for overcoating requires an understanding of the durability of these paint systems and a fuller understanding of the equivalent uniform annual cost as demonstrated in task A. A partial list of companies and State DOT's addressing the technical and economic aspects of overcoating include: Ocean City Research, Inc., BIRL, the industrial research laboratory at Northwestern University, IDOT, KTC, NCDOT, LADOT, VIDOT, WI-DOT, etc.

 

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