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Testing salt-spray test

Determination Test, Weight loss test, Eschke test, Salt spray test and Sulphur dioxide test at 50°C. Mechanism of inhibition of corrosion and surface study of mild steel was also studied by Metallurgical Resesarch Microscopy and Scanning electron Microscopy. [Pg.116]

Corrosion Testing. Salt spray testing (ASTM-B-117-52,54) was used to determine durability of adhesive bond in corrosive environment. Lap shear samples were exposed to salt spray for 14 days and then immediately tested for lap shear strength. [Pg.195]

Rubber cement tests Salt spray (fog) testing... [Pg.849]

Corrosion in Artificial Atmospheres Cosmetic Corrosion Test Metiiod for Automotive Parts Methods of Neutral Salt Spray Testing Salt Spray Test... [Pg.132]

In this study, PVC values ranged from 57.5 to 70.0% the variation of two consecutive PVC values was 2.5% in all cases. Preliminary laboratory tests (salt spraying chamber), with values of PVC from 10 to 70% for all formulations, helped to define the range of PVC more convenient to study (Sonawane et al., 2010). [Pg.162]

Product Utilization. The principal appHcation for chromium phosphate coatings is as a paint base for painted aluminum extmsions and aluminum beverage can stock. In these appHcations, extremely demanding performance criteria are met by the chromium phosphate conversion coatings. As an example, the Architectural Aluminum Manufacturer s Association Voluntary Specification 605.2-92 requires humidity and salt spray testing for 3000 hours and allows only minimal incidence of paint failure after testing (26). [Pg.224]

Formulation of effective corrosion-resistant coatings is made difficult by the lack of a laboratory test that can provide rehable predictions of field performance. The most widely used test is exposure in a salt fog chamber. It has been shown repeatedly, however, that the results of such tests do not correlate with actual performance (125). Outdoor exposure of panels can provide useful data, especially in locations where salt spray occurs, but predictions of performance are not always satisfactory (126). [Pg.350]

B287 acetic acid salt spray test... [Pg.110]

Sa.lt Spray Tests. One of the older accelerated corrosion tests is the salt spray test (40). Several modifications of this imperfect test have been proposed, some of which are even specified for particular appHcations. The neutral salt spray test persists, however, especially for coatings that are anodic to the substrate and for coatings that are dissolved or attacked by neutral salt fog. For cathodic coatings, such as nickel on steel, the test becomes a porosity test, because nickel is not attacked by neutral salt fog. Production specifications that call for 1000 hours salt spray resistance are not practical for quahty acceptance tests. In these cases, the neutral salt spray does not qualify as an accelerated test, and faster results from different test methods should be sought. [Pg.151]

The reproducibility of test results between labs using the neutral salt spray tests has not been consistent, but the repeatability, within one lab, is better, and the test has value in comparing variations in coating systems. Correlation of hours of exposure in the salt spray test to actual performance of the plated part in service, even in marine atmospheres, is not consistent and usually avoided. A classic example is that cadmium deposits outlast zinc deposits on steel in salt spray tests and clean marine atmospheres, yet zinc outlasts cadmium when exposed to real, industrial atmospheres, because of the presence of sulfur-bearing corrodents in industrial environments. An important variable in salt spray testing is the position of the surface to be tested. Whereas the surface of test panels is specified to be 15—30° from the vertical (40), when salt spray testing chromated zinc-plated specimens, this range has appeared excessive (41). [Pg.151]

The CASS Test. In the copper-accelerated acetic acid salt spray (CASS) test (42), the positioning of the test surface is restricted to 15 2°, and the salt fog corrosivity is increased by increasing temperature and acidity, pH about 3.2, along with the addition of cupric chloride dihydrate. The CASS test is used extensively by the U.S. automobile industry for decorative nickel—chromium deposits, but is not common for other deposits or industries. Exposure cycle requirements are usually 22 hours, rarely more than 44 hours. Another corrosion test, now decreasing in use, for decorative nickel—chromium finishes is the Corrodkote test (43). This test utilizes a specific corrosive paste combined with a warm humidity cabinet test. Test cycles are usually 20 hours. [Pg.151]

Salt spray tests, humidity tests, and other accelerated tests, some usiag sulfur dioxide and carbon dioxide, have shown favorable results for tin—2inc ia comparison with 2iac, cadmium, and fin deposits. Chromating improves the performance. [Pg.164]

As of this writing the 2inc alloys are too new to have actual corrosion resistance data, except for that based on accelerated tests. Zinc—nickel usually shows better results than 2inc-cobalt in salt spray tests. The reverse is tme when the Kesternich test is used. Tin—2inc performs well in both salt spray and Kesternich tests, but appears only to equal 2inc plating and 2inc—nickel in humidity tests. [Pg.165]

MSTM B117, Std Test Method of Salt Spray (Fog) Testings American Society for Testing and Materials, Philadelphia, Pa., 1990. [Pg.166]

In many commercial brochures, chemical resistance is indicated as excellent, good, fair, or poor. Although the test method is usually outlined, wide interpretation is possible. Immersion tests are usually described in this manner. Hydrolytic stabiUty is tested by salt-spray cycling or autoclave cycling. [Pg.265]

Corrosion-resistance test This can be done with the help of a salt spray test. The test piece is suspended in a salt spray chamber (Figure A13.6) for. seven days in 100% relative humidity (IS 101 and IS 11864). After the test, the surface should have no signs of deterioration or corrosion. [Pg.409]

Standard method for evaluation of painted or coated specimens subjected to corrosive environments Standard test method of salt spray (FOG) testing... [Pg.418]

Ductile and easily buffed chromium deposits having satisfactory corrosion resistance have been produced thus 0.005 mm-thick chromium deposits applied to steel by chemical deposition or by eiectrodeposition gave simiiar results when subjected to a salt-spray test . [Pg.437]

Resistance to corrosion Most authors who compare resistance to corrosion of electroless nickel with that of electrodeposited nickel conclude that the electroless deposit is the superior material when assessed by salt spray testing, seaside exposure or subjection to nitric acid. Also, resistance to corrosion of electroless nickel is said to increase with increasing phosphorus level. However, unpublished results from International Nickel s Birmingham research laboratory showed that electroless nickel-phosphorus and electrolytic nickel deposits were not significantly different on roof exposure or when compared by polarisation data. [Pg.537]

Even small traces of certain corrosion stimulants, notably soluble chlorides and sulphates, can maintain a continuing corrosion process under a paint film because the salts accelerate the initial dissolution of ferrous iron (and other metal ions) but are not immobilised in the hydrated oxide corrosion products. Filiform corrosion is the most spectacular example of this phenomenon, but progressive spread, preceded by blistering, is also observed from scratches or other breaks in a coating, for example during salt spray tests. [Pg.618]

Jaudon tested phosphate coatings with and without paint and found the salt-spray resistance, as judged by the first appearance of rust, to be as follows ... [Pg.715]

The most widely used accelerated tests are based on salt spray, and are covered by several Government Specifications. BS 1391 1952 (recently withdrawn) gives details of a hand-atomiser salt-spray test which employs synthetic sea-water and also of a sulphur-dioxide corrosion test. A continuous salt-spray test is described in ASTM B 117-61 and BS AU 148 Part 2(1969). Phosphate coatings are occasionally tested by continuous salt spray without a sealing oil film and are expected to withstand one or two hours spray without showing signs of rust the value of such a test in cases where sealing is normally undertaken is extremely doubtful. [Pg.716]

The main value of salt-spray tests is in the evaluation of the effectiveness of phosphate coatings in restricting the spread of rust from scratches or other points of damage in a paint film. This feature is of particular interest to the motorcar industry, as vehicles are often exposed to marine atmospheres and to moisture and salt when the latter is used to disperse ice and frost from road surfaces. Great care is needed in the interpretation of a salt-spray test, as it has been found to favour thin iron phosphate coatings more than is justified by experience with natural weathering. In the motorcar industry the present custom is to use zinc phosphate coatings on the car bodies and all other parts exposed to the outside atmosphere. [Pg.716]

Humidity tests are generally of more practical use than salt-spray tests, particularly where painting is employed, as the thoroughness of rinsing may be checked by this means. The use of contaminated water can leave... [Pg.716]

Table 15.13. This specification follows good industrial practice, with additional safeguards in rinsing to remove residues to treatment solutions. Nonaccelerated treatments must be followed by a single rinse which may contain chromate accelerated treatments must be followed by three rinses—cold water, hot water and a final chromate rinse. Table 15.14 shows the salt-spray test requirements for phosphate coatings with various finishes without formation of rust the paints and lacquer have the additional requirement that no rust shall be visible beyond 0-2 in (5 mm) from the deliberate scratches and no blistering, lifting or flaking beyond 0-05 in (1-27 mm) from the original boundaries of the scratches. Table 15.13. This specification follows good industrial practice, with additional safeguards in rinsing to remove residues to treatment solutions. Nonaccelerated treatments must be followed by a single rinse which may contain chromate accelerated treatments must be followed by three rinses—cold water, hot water and a final chromate rinse. Table 15.14 shows the salt-spray test requirements for phosphate coatings with various finishes without formation of rust the paints and lacquer have the additional requirement that no rust shall be visible beyond 0-2 in (5 mm) from the deliberate scratches and no blistering, lifting or flaking beyond 0-05 in (1-27 mm) from the original boundaries of the scratches.
The American Aeronautical Material Specification AMS 2480 A calls for 150h salt-spray test without rusting extending more than 0-125 in (3-175 mm) on either side of scratch marks, using a black enamel finish for the phosphate coating. [Pg.718]

The most common of the spray tests is the salt-spray or salt-fog test which was developed originally by Capp in 1914 for studying the protective values of metallic coatings on steel under conditions that he hoped would simulate exposure to a sea-coast atmosphere. Since then the test has been used for a number of purposes, for many of which it is not well suited Although there is no standard size or shape of salt-spray box certain other features of the test have been standardised in ASTM B117 1990. Various... [Pg.1022]

Fig. 19.11 Effect of specimen position on corrosion in salt-spray tests specimens of cold-rolled steel, (a) 20% NaCl, (i>) synthetic sea-water... Fig. 19.11 Effect of specimen position on corrosion in salt-spray tests specimens of cold-rolled steel, (a) 20% NaCl, (i>) synthetic sea-water...
The results will also be influenced by the concentration of NaCl solution sprayed —some metals are affected more by one concentration than another — for example, zinc is corroded most by a concentrated brine (20%), while iron is corroded most by a dilute brine (3%) synthetic sea-water is less corrosive to these metals than either brine. In view of the many other ways by which the conditions within a salt-spray box differ from those of exposure to a natural sea-coast environment, there seems to be no great advantage in making-up complicated synthetic sea-waters for use in salt-spray testing. However, tablets for this purpose are commercially available. [Pg.1023]


See other pages where Testing salt-spray test is mentioned: [Pg.477]    [Pg.493]    [Pg.2117]    [Pg.332]    [Pg.223]    [Pg.110]    [Pg.165]    [Pg.2425]    [Pg.259]    [Pg.359]    [Pg.439]    [Pg.440]    [Pg.453]    [Pg.511]    [Pg.514]    [Pg.718]    [Pg.720]    [Pg.978]    [Pg.1023]    [Pg.1024]    [Pg.1025]   
See also in sourсe #XX -- [ Pg.203 , Pg.207 ]




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Acetic acid-salt-spray test

Assemblies and Salt Spray or Immersion Testing

Cabinet corrosion tests salt spray test

Copper-accelerated acetic acid-salt spray testing (ASTM

Copper-accelerated salt spray test

Corrosion protection salt spray test

Corrosion resistance salt spray tests

Electrodeposition salt spray test

Industrial salt spray testing

Modified salt spray testing

Neutral salt-spray test (ASTM

Organic coatings salt spray test

Phosphating salt spray tests

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Salt Spray (Fog) Testing

Salt Spray Test Results

Salt spray fog test

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Salt spray testing (ASTM

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Salt spray testing method

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