diverse range of coatings for use in a wide variety of indus- tries. For example, coatings such as alkyds, acrylics, vinyls, epoxies, urethanes, polyureas, silicones, and silicates can be used to coat structures of such variety as bridges, railroad cars, chemical process vessels, elevated water tanks, and concrete floors. Therefore, it is obvious that because of the many different coating chemistries and the vast range of environments to which they might be exposed, the testing of industrial maintenance coatings can be a broad topic. Furthermore, a particular physical property which may be important in one application, such as temperature resis- tance for a stack coating, may be of little importance for a different coating in a different environment. Therefore, it is important to know not only what type of tests can be run, but to appreciate the relative importance of various tests, realizing that their ranking may change from project to project. In broad terms, the testing of coatings falls into one of two categories: determining the properties of the liquid paint, and determining the properties of the dried film. The testing of liquid paint can involve not only determin- ing compositional related parameters such as density or solids content, but also application related parameters such as dry time and sag resistance. Although dried films can certainly be subjected to a barrage of analytical techniques to investigate chemical composition, this would generally be considered a separate topic, and in the context of this chapter most of the testing on dried films is done to deter- mine performance or physical properties, such as abrasion resistance or adhesion. In the past, much emphasis, not only in testing but in specification writing, was placed on the chemical composi- tion of the coating. In the last decade or so, the emphasis has shifted more toward performance based requirements. Although the performance of the coating on the substrate is certainly of more fundamental importance than which ingredients are in the can, the latter should not be ignored. Indeed, it is fairly common when screening coatings for a Qualified Products List (QPL) to base acceptance on their performance characteristics, but also to do some basic compositional testing of the specific batch which was sub- mitted. The results of these compositional tests are then used to define the characteristics of any future batches which may be provided for specific jobs, to help insure that production batches have similar composition (and there- fore hopefully similar performance characteristics) to the batch which passed the QPL testing. TESTING OF LIQUID COATINGS Density The density, or weight/gallon, of a liquid coating is a rapid, inexpensive test which, when combined with a few other simple tests, provides a measurement indicative of the types and relative amounts of ingredients making up the coating. Indeed, a significant variation in density is a sign that a production error has probably occurred. The density of a material is generally performed with a pycnometer, which is simply a device which has a spe- cific, known volume at a certain temperature. In the paint industry, the pycnometer is known as a weight-gallon cup, and the test is performed in accordance with ASTM D1475 (Standard Test Method for Density of Liquid Coatings, Inks, and Related Products). Briefly, a slight excess of material is placed in the cup, such that when the lid is attached the excess is forced out through a small hole in the center of the lid. This assures that the cup is completely filled. The cup and lid are weighed before and after, and the grams of liquid paint can then be used to determine the density of the paint, in lbs/ gal. Often, the density of the paint in lbs/ gal is simply the weight of the paint contained in the cup, in grams, divided by 10. Solids by Weight The percent solids by weight of a coating, often referred to as its percent nonvolatile by weight, is usually determined in accordance with ASTM D2369 (Standard Test Method for Volatile Content of Coatings). Basically, a liquid coating consists of four types of ingredients: resins or polymers, pigment, additives, and solvents. By determining the solids by weight, one is determining the combined amount of the first three ingredients. Since these are the ingredients left behind in the dried film, it is important that a particular production batch have the correct solids content. Basically, the test method involves weighing a certain amount of liquid coating into a previously weighed thin, dis- posable aluminum dish, baking this in an oven for 1 hour at 105 to 115C, and dividing the weight of solid material left behind by the initial weight of liquid material used. The procedure is simple and straightforward, although the precision and accuracy for thick, high solids multi- component coatings is not quite as good as for simple low solids coatings such as alkyds. In some such cases, these coatings contain curing agents which are volatile at the temperature of the test, meaning that they can evaporate in the oven before they get a chance to cross-link and become nonvolatile. This possibility is recognized by ASTM, and 63 Testing of Industrial Maintenance Coatings Dwight G. Weldon 1
1 Weldon Laboratories, Inc., 1188 Route 30, P.O. Box 40, Imperial, PA 15126. MNL17-EB/Jan. 2012 Copyright 2012 by ASTM International www.astm.org
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized. CHAPTER 63 TESTING OF INDUSTRIAL MAINTENANCE COATINGS 779 for such coatings it is recommended that they be allowed to air dry for one hour after mixing and prior to placing them in the oven. Single component reactive coatings, such as moisture cured urethanes, are not specifically addressed by ASTM. However, it would seem logical to treat them in a similar fashion to the reactive two component coatings. Volume Solids The percent solids by volume of a coating, often referred to as its volume solids, is determined in accordance with ASTM D2697 (Standard Test Method for Volume Non- volatile Matter in Clear or Pigmented Coatings). This is a somewhat more complicated test than either the density or weight solids tests described above, and indeed requires that these two tests be done in order to perform the neces- sary calculations. Essentially, the liquid coating is applied to small metal disks and allowed to dry. The disks are then weighed in air, and again while suspended in water, and the appropriate calculations are done to determine the percent, by volume, of the nonvolatile material in the coating. Not only is volume solids an important property relat- ing to the composition of the coating, but it has important practical significance. If the coating is supposed to be 70 % solids by volume and is to be applied at 10 mils wet, it will dry to a thickness of 7 mils. If a batch were low in solids, say 50 % versus 70 %, and if the applicator still applied it at the recommended 10 mils wet, he would only get a dry film thickness of 5 mils, rather than the expected 7 mils. Viscosity There are many ways to measure the viscosity of a coating. These include determining the time it takes for a coating to drain from a cup of known volume through an orifice of known size (ASTM methods D4212Standard Test Method for Viscosity by Dip-Type Viscosity Cups, and D1200Stan- dard Test Method for Viscosity by Ford Viscosity Cup), the use of rotational viscometers using spindles, such as Brook- field viscometers (ASTM D2196Standard Test Methods for Rheological Properties of Non-Newtonian Materials by Rotational (Brookfield type) Viscometer), and rotational viscometers using paddles, such as the Stormer viscometer (ASTM D562Standard Test Method for Consistency of Paints Measuring Krebs (KU) Viscosity Using the Stormer- Type Viscometer). Brookfield viscometers can produce a much more accurate viscosity profile than a Stormer vis- cometer, because they allow one to obtain viscosity data over a wide range of shear rates. In contrast, a Stormer viscometer (Fig. 1) provides only a single data point, with the viscosity (expressed as Krebs Units, or KU) being deter- mined under a single, low shear condition. Nevertheless, partly because of its simplicity, the standard quality control test for viscosity is done with the Stormer type viscometer. When performing viscosity testing, it is important that the temperature requirements be observed, as this can sig- nificantly affect the results. It is also important to realize that the viscosity of a multi-component coating can change over time, and that viscosity should be determined as soon after mixing as possible. Pigment Content The weight solids test described above provides a measure of the total amount, by weight, of solid material in the liquid coating. It says nothing, however, about the ratio of pigment to vehicle, which can have a significant influ- ence on the performance of the coating. The common procedures for determining percent pigment are ASTM D2371 (Standard Test Method for Pigment Content of Solvent-Reducible Paints) for solvent borne coatings, and ASTM D3723 (Standard Test Method for Pigment Content of Water-Emulsion Paints by Low-Temperature Ashing) for water-borne coatings. The first procedure involves using a centrifuge to separate the pigment from the vehicle and sol- vents, while the latter involves ashing a dried film of coating after first determining its weight solids. Once a sample has been analyzed for percent pigment and weight solids, the percent vehicle can be calculated simply by taking the dif- ference between the two. The only error in this procedure, which is usually quite minor, is the inclusion of any addi- tives as vehicle. Sag Resistance Sag resistance provides a measure of how thick a coating can be applied to a vertical surface before it begins to sag. This is important, because if the coating is intended to be applied at 10 wet mils but sags at 5, it will have to applied in two coats rather than one. Sag resistance is commonly tested in accordance with ASTM D4400 (Standard Test Method for Sag Resistance of Paints Using a Multinotch Applicator). This involves preparing a drawdown using a notched applicator (Fig. 2) which applies the coating in a pattern of stripes covering a range of thicknesses. The drawdown is then immediately hung vertically, with the thinnest stripe at the top and the thickest at the bottom, and subsequently evaluated to determine the heaviest thickness which does not sag into the stripe below it. Fig. 1Stormer viscometer used to obtain viscosity of coatings. (Photograph courtesy of Weldon Laboratories.)
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized. 780 PAINT AND COATING TESTING MANUAL 15TH EDITION Drying Time How long it takes a coating to dry to touch, or dry hard, can be an important practical consideration. Furthermore, if the drying time of a particular batch is very much lon- ger than expected, it could be an indication of a compo- sitional problem. Drying time is commonly measured in accordance with ASTM D1640 (Standard Test Methods for Drying, Curing, or Film Formation of Organic Coatings at Room Temperature). The tests are simple but subjective, and involve such techniques as touching with ones finger to determine set to touch times, or using a twisting motion with ones thumb to determine dry to handle times. Infrared Spectroscopy Most of the above tests are rapid, require relatively inex- pensive equipment, and provide a quick screening method to determine if a particular batch of coating falls within specification requirements. However, they essentially mea- sure some type of bulk property which, although dependent to some extent on the specific ingredients of the coating, does not in any way actually identify these ingredients. A powerful tool for providing compositional information on paints and coatings, whether in the solid or liquid state, is infrared spectroscopy. Infrared spectroscopy is described in great detail else- where in this volume. Simply put, it allows a material to be identified by measuring the amount of infrared light absorbed (or transmitted) at various frequencies. Indeed, a spectrum is simply a graph showing the amount of absorbed (or transmitted) infrared light as a function of fre- quency. Two examples of infrared spectra are shown in Fig. 3. Even without understanding the underlying theory of the process, it is obvious that the spectrum of the vinyl latex is much different in appearance than the spectrum of the Fig. 2A multinotch applicator used to evaluate sag resis- tance. (Photograph courtesy of Weldon Laboratories.) Fig. 3Infrared spectra of an epoxy (top) and a vinyl latex (bottom). (Photograph courtesy of Weldon Laboratories.)
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized. CHAPTER 63 TESTING OF INDUSTRIAL MAINTENANCE COATINGS 781 epoxy. The fact that different materials each have their own unique infrared spectrum has led to them being referred to as fingerprints. In recent years there has been a trend in product test- ing to obtain an infrared spectrum of the batch of coating submitted for testing. If the batch passes all the testing requirements and is approved, the spectrum is kept on file in the event that a problem occurs with a later, production batch of coating. If the spectrum shows a marked devia- tion in composition from the originally approved batch, it is likely that the problem is a coating one. On the other hand, if the various bulk properties are consistent, and the spectrum is a good match to the spectrum of the approved batch, it is likely (but not certain) that the problem lies elsewhere. Although an extremely useful technique, infrared spec- troscopy is not without its limitations. First of all, there is more than one way to actually obtain a spectrum of a sam- ple, and the analyst must be consistent in his methodology in order to obtain reproducible spectra. Secondly, infrared spectroscopy generally cannot detect ingredients which are present at less than 4 % or 5 % unless they are somehow separated or at least partially isolated from the mixture. Therefore, a minor additive which might have a crucial bear- ing on the performance of a coating, such as an ultraviolet light absorber, would not even be detected by this technique. TESTING OF APPLIED COATINGS Because of the diversity of coating types, structures, and environments encountered in the industrial maintenance field, there are numerous tests which could be appropriate for a given situation. Because of this, the first question to ask when putting together a testing program, or evaluat- ing the manufacturers published literature, is what is this coating going to be used for?. This simple question will help greatly in deciding which tests are appropriate, and how much emphasis to place on each test. The follow- ing is a list of many of the common tests which could be appropriate for evaluating the performance of an industrial maintenance coating. ASTM D6577 (Standard Guide for Testing Industrial Protective Coatings) provides a good list of the many tests available. Adhesion Of all the physical and chemical properties of a coating, this one is arguably the most important. The best coating will offer little protection if it does not stick to the substrate. There are several methods to measure adhesion, including such subjective, unofficial techniques as prying with a hammer and chisel to rubbing with the edge of a coin. The three more widely used standardized ASTM techniques, however, include D3359, D4541, and D6677. ASTM D3359 (Standard Test Methods for Measur- ing Adhesion by Tape Test) is often referred to as tape adhesion. There are two methods to choose from, A and B, depending on the thickness of the coating. Method A is recommended for films greater than 5 mils thick, and involves using a cutting tool to scribe an X cut into the specimen, followed by the application of a special pressure sensitive adhesive tape. The tape is then rapidly removed, and the adhesion is assessed in accordance with the methods descriptive rating system. The ratings range from a 5 for no peeling or removal, to a 0 for removal beyond the area of the X. Method B, for thinner films, involves scribing a cross-hatch pattern into the specimen, again fol- lowed by the application and removal of tape. The ratings, which also range from 5 to 0, are assessed in accordance with pictorial representations of the percentage of coating removal. The technique has the advantage of being quick, simple, and inexpensive, and can even be done on curved surfaces. However, occasionally problems can be encoun- tered with the tape not adhering well to the paint, resulting in artificially good results. A more common problem, how- ever, especially with thick, tough coatings, is not being able to scribe completely through to the substrate. ASTM D4541 (Standard Test Method for Pull-Off Strength of Coatings Using Portable Adhesion Testers) is often referred to as tensile adhesion. It involves using an adhesive to attach aluminum or steel dollies or stubs to the coating, and then using some sort of portable adhesion tester (Fig. 4) to measure the force required to pull the stub from the surface, hopefully taking the coating along with it. The result is reported in psi. A variation of this test is cur- rently being evaluated for use on coated concrete. The advantages of this method compared to D3359 include less subjectivity and less operator error associ- ated with not cutting completely through the coating. It has several potential drawbacks, however, not the least of which is the fact that the various instruments on the mar- ket can produce widely varying results. Thus, it is critical, when performing the test, to report which instrument was used, and results between one coating and another should only be compared if they were tested using the same type of instrument. It is also not uncommon for the precision to be relatively poor, at least for certain types of instru- ments, so it is advisable to perform testing in duplicate or triplicate. The method can usually not be used on curved sur- faces, as this changes the degree of contact and hence the surface area tested, and, once the stubs are applied, it can take from a few hours to overnight before the adhesive has cured enough to test. Furthermore, some adhesives do not bond well to the surfaces of some coatings, resulting in glue failures rather than coating delamination. It should also be pointed out that it is not unusual for tensile adhesion and tape adhesion results to appear to be inconsistent. This is Fig. 4A type of commonly used portable adhesion tester. (Photograph courtesy of Weldon Laboratories.)
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized. 782 PAINT AND COATING TESTING MANUAL 15TH EDITION likely because tape adhesion applies a significant degree of shear stress to the coating, which is absent in the tensile testing. Thus, the coating adhesion, when assessed by tape adhesion, can sometimes appear to be worse than the ten- sile adhesion values would indicate. A third, relatively new ASTM method for assessing adhesion, is D6677 (Standard Test Method for Evaluating Adhesion by Knife). This method involves using a knife to cut an X into the sample, and then uses the tip of the knife to pick or probe at the intersection of the cuts. There is a rating system based on the ease with which the coating can be removed. Investigators and inspectors have used similar methods for years in subjectively determining coating adhe- sion, and one of the main reasons for establishing D6677 was to try to standardize, at least to some extent, the vari- ous subjective methods in use. Corrosion Resistance When the structure being painted is made of steel, assess- ing the corrosion resistance of the coating is very impor- tant. By far the most commonly used procedure is the salt spray test, ASTM B117 (Standard Practice for Operating Salt Spray (Fog) Apparatus). The test involves placing the painted panels in a salt spray cabinet (Fig. 5), which essen- tially produces a fog of warm (95F) saltwater (5 % sodium chloride). After an agreed upon period of time, such as 1000h, the panels are evaluated for such things as blister- ing (ASTM D714Standard Test Method for Evaluating Degree of Blistering of Paints), rusting (ASTM D610Stan- dard Practice for Evaluating Degree of Rusting on Painted Steel Surfaces), and undercutting at the scribe (ASTM D1654Standard Test Method for Evaluation of Painted or Coated Specimens Subjected to Corrosive Environments), if the panels were scribed (an option) before placing them on test. The procedure has been used for decades, and is firmly entrenched in many specifications. Over the last ten years or so, however, it has become somewhat controversial, and there is a body of evidence that salt spray results do not cor- relate very well with real world performance. A second commonly used test procedure which has increased substantially in popularity over the last several years is what is known as Prohesion testing, which is described in ASTM D5894 (Standard Practice for Cyclic Salt Fog/UV Exposure of Painted Metal). The terminology, however, is somewhat confusing, as Prohesion testing refers to a procedure involving a cyclic salt fog test, which is only one component of D5894 (the other component being accel- erated weathering). In D5894, the test panels (either scribed or unscribed) are placed in a cyclic salt fog cabinet (sometimes referred to as a Prohesion cabinet), which introduces a fog of dilute salt water (0.05 % sodium chloride/0.35 % ammonium sulfate) at room temperature for one h. After one h, the cabinet is purged with warm, dry air for one hour, and the cycle is repeated. The panels remain in the cyclic salt fog cabinet (also described in ASTM G85, Standard Practice for Modified Salt Spray (Fog) Testing) for a specified period of time (typi- cally one week), after which time they are manually trans- ported to an ASTM G154 accelerated weathering cabinet, which uses ultraviolet light, heat, and moisture to weather the panels, again typically for one week. The panels alter- nate between the two cabinets, typically for a total duration of 1000 h, and are then evaluated in the manner described above for salt fog testing. It is generally felt that D5894 gives better correlation to the real world performance of coatings than does B117. However, in both cases, and indeed with all accelerated laboratory test methods, it is extremely difficult to use the tests to actually predict the service life of a coating system. The tests are primarily used to compare one coat- ing with another, allowing them to be ranked as to which can be expected to perform the best. There is also concern that D5894 gives artificially poor results for zinc-rich primers. Accelerated Weathering A commonly asked question of a coating is how durable is it, or how well does it weather. The best, but also the slowest way, to answer this question is to expose painted panels outdoors in an environment similar to what might actually be expected. As this can take years, there have been various accelerated laboratory test methods developed. All of these methods employ a combination of heat, ultravio- let light, and moisture to weather or degrade the coating. Broadly speaking, they fall into two categories, depending on the source of ultraviolet light: arc devices, and fluores- cent tube devices. Arc devices produce ultraviolet light by passing an electrical current through an electrode. Devices include enclosed and open-flame carbon arcs described by ASTM G153 (Standard Practice for Operating Enclosed Carbon Arc Light Apparatus for Exposure of Nonmetallic Materi- als) and D822 (Standard Practice for Filtered Open-Flame Carbon-Arc Exposures of Paint and Related Coatings), and Fig. 5An ASTM B117 salt fog cabinet. (Photograph courtesy of Weldon Laboratories.)
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized. CHAPTER 63 TESTING OF INDUSTRIAL MAINTENANCE COATINGS 783 xenon arc machines described by ASTM G155 (Standard Practice for Operating Xenon Arc Light Apparatus for Exposure of Non-Metallic Materials). In all cases, water is sprayed intermittently onto the specimens as a fine mist, and exposure to light and darkness is alternated. A com- monly used cycle is 102 min of light at 145F and 18 min of light and water spray at 60F. The xenon arc devices have become much more common than the carbon-arc devises. Fluorescent UV bulb devices are described in ASTM G154 (Standard Practice for Operating Fluorescent Light- Apparatus (for UV) Exposure of Nonmetallic Materials), formerly known as ASTM G53. Briefly, they use fluorescent tubes to provide the ultraviolet light, and moisture in the form of condensation is produced by heating a trough of water located in the bottom of the instrument. Many differ- ent types of bulbs are available which have different spec- tral characteristics, although most fall into what is known as either the UV-A or UV-B region of the electromagnetic spectrum. The UV-B region is more aggressive and can pro- duce results in less time, but the UV-A region is generally felt to be a more realistic test. Regardless of which type of test is selected it must be kept in mind that it is very difficult, if not impossible, to predict an actual lifetime for a coating based upon accel- erated weathering data. Weather varies dramatically from geographic region to geographic region, and even from year to year in the same region. Therefore, the primary use of accelerated weathering is to compare or rank one coating versus another. Chemical Resistance When one considers all the industrial environments that painted structures can be exposed to, as well as the fact that coatings are used to protect such things as waste water treatment plants, off shore oil platforms, secondary containments, and even the interiors of railroad tank cars and chemical process vessels, it is apparent that chemical resistance is an extremely important property. The two rel- evant test methods for determining chemical resistance are ASTM D1308 (Standard Test Method for Effect of House- hold Chemicals on Clear and Pigmented Organic Finishes), and ASTM C868 (Standard Test Method for Chemical Resis- tance of Protective Linings). The title of D1308 is somewhat misleading, as the methodology can be applied to harsh industrial chemicals as well as mild household ones. The method is broadly written, and covers such possibilities as simple room tem- perature spot testing, where a small amount of chemical is applied to a test panel and covered with a watch glass for an hour or so, to high temperature immersion testing. The method does not go into much detail as to apparatus, time, or temperature, and basically leaves these decisions up to the investigator. Obviously, chemicals should be chosen which could reasonably come into contact with the coating, and realistic, although perhaps slightly elevated, tempera- tures should be chosen. Although in service the coating may be expected to perform for several years, laboratory testing is usually carried out for no more than a few months, with the panels being evaluated for such things as rusting, blis- tering, cracking, softening, or delamination. If the coating goes for a few months with little or no sign of deterioration, it is generally assumed to be acceptable for that chemical, even though it is not possible to predict the actual service life in years. While D1308 involves immersion testing, C868 is often referred to as one-sided immersion testing, or sometimes Atlas Cell testing, even though there may be a number of companies which manufacture the equipment. A virtually identical test is described in NACE TM-01-74 (Laboratory Methods for the Evaluation of Protective Coatings and Lin- ing Materials in Immersion Service). The apparatus used in C868 (Fig. 6) consists of a glass cylinder, typically 5 to 7 in. in diameter, fitted with ground glass take offs for such things as condensers, thermometers, or immersion heaters (one variety jackets the outside of the cell with a flexible heating element). The gasketed test panels actually form the two ends of the cell. The cell is then filled halfway to two thirds full with the chemical of interest, and the heating ele- ment set to maintain the desired test temperature. The test duration is typically from 3 to 6 months. One of the main advantages to C868 testing is that, since the test panels are not immersed, there are no edge effects to worry about. Sometimes it is difficult to seal sharp edges, and failures can occur near edges which are more application related than coating related. Another advantage to C868 testing, which depending on circumstances may be more perceived than real, is the belief that it mimics the cold wall effect. The cold wall effect has been observed numerous times, and occurs when the outside, non-immersed surface of the steel is colder than the inner surface which is exposed to the contents of the vessel. This is a more aggressive condition than if the inner and outer temperatures are the same, and can more readily cause blistering of the interior coatings. Fig. 6An ASTM C868 chemical resistance cell. (Photograph courtesy of Weldon Laboratories.)
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized. 784 PAINT AND COATING TESTING MANUAL 15TH EDITION At first glance, this condition would appear to be simulated in Atlas Cell testing. However, unless the steel test panels are rather thick, there is actually very little dif- ference in temperature between the inner and outer walls. A temperature gradient can be imposed by jacketing the outer surface with a cell containing circulating water, but in practice this is rarely done. When doing chemical resistance testing, it is tempt- ing to choose a temperature much higher than the actual, expected temperature, in order to accelerate the test. Care must be taken, however, not to choose too high of a tem- perature. If the coating is below its glass transition temper- ature when in actual service, but has been artificially raised above its glass transition temperature during laboratory testing, the possibility exists that it will have been made more permeable as a result. Thus, it could fail in the labora- tory, yet in actual service it could perform very well. Abrasion Resistance Coatings used to protect handrails or used in areas sub- jected to heavy foot traffic need to be resistant to abrasion. By far the two most popular methods to evaluate abrasion resistance include Taber abrasion and falling sand. Taber abrasion testing is described by ASTM D4060 (Standard Test Method for Abrasion Resistance of Organic Coatings by the Taber Abraser). The test panels, which are 4 4 in. 2 with a hole in the middle, are mounted on a device called a Taber abrader. This is essentially a turntable with a pair of weighted abrading wheels which rest on the panel. As the panel rotates, the abrasive wheels turn along with it, resulting in removal of some or all of the coating. The panels are weighed before and after testing, and the result is usually reported as a weight loss per so many cycles (usually 1000 cycles). Coatings with better abrasion resis- tance lose a smaller amount of weight. When evaluating Taber abrasion results, it is important to know the number of cycles, the load on the wheels, and the type of wheels. CS-17 wheels are the most common, but wheels of lesser and greater abrasiveness can be used. The falling sand test is described by ASTM D968 (Stan- dard Test Methods for Abrasion Resistance of Organic Coatings by Falling Abrasive). Essentially, the test panel is mounted at a 45 angle beneath a tube which is attached to a hopper. A known quantity of sand is dumped into the hopper and impinges upon the test panel. The amount of sand required to wear through the coating is reported. On relatively thin, ordinary coatings such as an acrylic latex or an alkyd, the test is relatively simple to do. On a thick, high performance coating such as an epoxy or an elastomeric urethane the test can be extraordinarily time consuming, and requires large quantities of sand (an individual quan- tity of sand is to be discarded after a certain number of uses). Impact Resistance Examples of coatings which would require good impact resistance would include coatings for overseas shipping containers, and coatings for use on locks and dams. Most- impact resistance tests involve dropping a weight onto a coated panel and looking for cracking or disbonding. The most common procedure is ASTM D2794 (Standard Test Method for Resistance of Organic Coatings to the Effects of Rapid Deformation (Impact), where a hemispherical tup is rested on the panel, and a falling weight, housed in a guide tube, is dropped from varying heights to determine the greatest force, expressed in in-lbs, which will not crack or disbond the coating (Fig. 7). The procedure calls for the use of a thin gage steel panel which will deform under the conditions of the test, although many users prefer to use thicker steel representative of the actual article to be coated. If the weight is dropped on the coated face, the result is referred to as direct impact. If it is dropped on the back of the panel, it is referred to as indirect or reverse impact. Coatings nearly always have lower reverse impact than they do direct impact resistance. Flexibility A certain amount of flexing or movement is common with many structures. Electrical transmission towers flex and move in the wind, thin galvanized decking can flex when walked upon, and metal can change dimensions slightly upon freezing and thawing. Furthermore, instantaneous flexing can occur when a surface is subjected to a sharp impact. Indeed, it is difficult to imagine a case where flex- ibility would not be a desirable property of a coating. The fact that not all coatings are flexible is because to impart flexibility to a coating, one must often sacrifice other properties, such as chemical resistance or resistance to permeation. Coatings are commonly tested for flexibility by bend- ing a coated, thin gauge steel or aluminum panel over a mandrel and examining the coating for cracking, in accor- dance with ASTM D522 (Standard Test Methods for Man- drel Bend Test of Attached Organic Coatings). The method Fig. 7A variable impact tester used to measure the impact resistance of coatings. (Photograph courtesy of Weldon Laboratories.)
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized. CHAPTER 63 TESTING OF INDUSTRIAL MAINTENANCE COATINGS 785 describes two procedures, one using a conical mandrel, and one using cylindrical mandrels. The conical mandrel consists of a metal cone, 8 in. in length, with a diameter of 1/8 ft at the narrow end to 1 1/2 in. at the wide end (Fig. 8). There are clamps for mounting the panel, and a rotating arm which is used to bend the panel around the mandrel. If the coating is being evaluated for percent elongation, it is bent slowly (over a period of 15 s). If it is being evaluated for crack resistance it is bent quickly (approximately 1 s). If cracking occurs, the distance which the cracking extends from the small diameter end towards the large diameter end is measured and used to determine the coatings percent elongation. If no cracking occurs, the percent elongation is greater than approxi- mately 32 percent. When using cylindrical mandrels, one usually simply reports the smallest diameter mandrel over which the panel can be bent without cracking, although % elongation can also be estimated. The mandrel testing described in D522 is usually sufficient for testing most industrial maintenance coat- ings. However, for very flexible elastomeric coatings it is of little use, since these coatings will have elongations of 100 % or more, far above the maximum 32 % which can be determined by D522. In such cases, it may be desirable to test such coatings using the so-called universal test- ing machines, which essentially use clamps to hold free, unsupported films of coatings between the jaws of the machine. The sample is then stretched apart at a known rate and a stress-strain curve obtained. Such properties as percent elongation, tensile strength, and modulus (essen- tially the stiffness of the sample) can be determined. Applicable test procedures include D2370 (Standard Test Method for Tensile Properties of Organic Coatings) and D638 (Standard Test Method for Tensile Properties of Plas- tics). It is often difficult, however, to test very thin free film coatings by these methods, although coatings thicker than about 5 mils can usually be tested. Moisture Resistance A coating intended to line the interior of a potable water tank obviously requires good moisture resistance. While salt spray and accelerated weathering tests have a moisture component to them, they introduce other elements which the potable water lining would not be exposed to. Since water could certainly be considered a chemical, some type of water immersion test could certainly be carried out in accordance with the general chemical resistance testing previously described by ASTM D1308. However, water or moisture resistance is more commonly done in accordance with either ASTM D4585, D2247, or D1735. ASTM D4585 (Standard Practice for Testing Water Resis- tance of Coatings Using Controlled Condensation) involves generating water vapor by heating a pan of water located in the bottom of the chamber. The test panels form the roof or walls of the chamber, and since their back side is exposed to the cooler air of the laboratory, condensation forms on the coated front surfaces. Although this sounds like a relatively gentle test, it is actually quite aggressive since the condens- ing water is relatively pure and it is conducted at a slightly elevated temperature. Coatings typically fail by blistering. ASTM D2247 (Standard Practice for Testing Water Resis- tance of Coatings in 100 % Relative Humidity), is somewhat similar, except that the cabinet is designed differently and the specimens are completely suspended inside the chamber. Considerably different than the above methods is ASTM D1735 (Standard Practice for Testing Water Resis- tance of Coatings Using Water Fog Apparatus). This method uses a chamber similar to an ASTM B117 salt fog cabinet to expose the panels to an actual mist of water. Hardness Industrial maintenance coatings are commonly rated for hardness using the pencil hardness method described in ASTM D3363(Standard Test Method for Film Hardness by Pencil Test). In this method, a series of pencils is used to determine the hardest pencil lead which will not scratch or gouge the coating. The pencil ratings, from softest to hard- est, are as follows: 6B-5B-4B-3B-2B-B-HB-F-H-2H-3H-4H-5H-6H The test is somewhat subjective, not only because of operator variability, but also because of possible variations among different sets of pencils. ASTM lists a reproducibility of plus or minus one pencil. For thick coatings, hardness is sometimes determined using some type of indentation tester. The two most commonly used are the Barcol (D2583) and Durom- eter (D2240Standard Test Method for Rubber Property- Durometer Hardness) types. In both cases, hand pressure is used to drive a spring loaded indenter into the coating, and the ease of penetration is reflected on the scale (higher numbers indicate harder coatings). Water Vapor Permeability It is not surprising that a coatings resistance to the perme- ation of water vapor can have a significant bearing on its ability to protect the substrate. In many cases, this is tested in a very practical way by subjecting painted test panels to wet or humid environments, such as the salt spray, accel- erated weathering, and humidity tests described above. A more direct way to actually measure the rate of water vapor permeation, however, is described in ASTM D1653 (Standard Test Methods for Water Vapor Transmission of Organic Coating Films). In this test method, free films of coating (or films attached to a thin, porous paper substrate) are sealed to the open mouth of a cup or dish, and essen- tially form the lid of the cup (Fig. 9). In Method A the cup Fig. 8A conical mandrel tester used to determine per cent elongation. (Photograph courtesy of Weldon Laboratories.)
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized. 786 PAINT AND COATING TESTING MANUAL 15TH EDITION contains a desiccant, and the assembly is placed in a humid environment. The cup is weighed periodically to measure the amount of moisture which has passed through the coating and into the desiccant. In Method B, which is the more common procedure, the cup contains water, and is placed in a dry environment. It is then weighed periodically to determine the amount of moisture which has passed through the coating and out of the cup. Theoretically the procedure sounds very simple and straightforward. In practice, however, it is not quite so simple. It can sometimes be extremely difficult to obtain, as the method calls for, smooth and completely continu- ous films of uniform thickness throughout the test area. Furthermore, if the coatings are very thin, or very brittle, it can be a frustrating task to remove them from the release paper or even mount them on the cups without tearing or fracturing them. Fig. 9A permeability cup used to determine water vapor transmission. (Photograph courtesy of Weldon Laboratories.)
Copyright by ASTM Int'l (all rights reserved); Mon Feb 4 01:24:12 EST 2013 Downloaded/printed by North Carolina State Univ pursuant to License Agreement. No further reproductions authorized.