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MIL-STD-202G

NUMERICAL INDEX OF TEST METHODS

Test Method

 

Date

 

Title

 

Number

 

 

 

 

 

 

 

 

Environmental tests (100 class)

 

101E

 

February 2002

 

Salt atmosphere (corrosion)

(formerly called salt spray)

8

 

102A

Cancelled

 

Superseded by Method 107

(see note on Method 102)

103B

12

September 1963

 

Humidity (steady state)

 

104A

24

October 1956

 

Immersion

 

105C

12

September 1963

 

Barometric pressure (reduced)

 

106G

8

February 2002

 

Moisture resistance

 

107G

28

March 1984

 

Thermal shock

 

108A

12

September 1963

 

Life (at elevated ambient temperature)

 

109C

8

February 2002

 

Explosion

 

110A

16

April 1973

 

Sand and dust

 

111A

16

April 1973

 

Flammability (external flame)

 

112E

11

October 1988

 

Seal

 

 

 

Physical characteristics tests (200 class)

 

201A

 

October 1956

 

Vibration

 

24

 

 

202D

Cancelled

 

Superseded by Method 213

(see note on Method 202)

203C

8

February 2002

 

Random drop

 

204D

1

April 1980

 

Vibration, high frequency

 

205E

Cancelled

 

Superseded by Method 213

(see note on Method 205)

206

12

September 1963

 

Life (rotational)

 

207B

8

February 2002

 

High-impact shock

 

208H

31

January 1996

 

Solderability

 

209

18

May 1962

 

Radiographic inspection

 

210F

8

February 2002

 

Resistance to soldering heat

 

211A

14

April 1969

 

Terminal strength

 

212A

16

April 1973

 

Acceleration

 

213B

16

April 1973

 

Shock (specified pulse)

 

214A

28

March 1984

 

Random vibration

 

215K

8

February 2002

 

Resistance to solvents

 

216

Cancelled

 

Superseded by Method 210

(see note on Method 216)

217A

8

February 2002

 

Particle impact noise detection (PIND)

 

 

 

Electrical characteristics tests (300 class)

 

301

 

February 1956

 

Dielectric withstanding voltage

 

6

 

 

302

6

February 1956

 

Insulation resistance

 

303

6

February 1956

 

DC resistance

 

304

24

October 1956

 

Resistance temperature characteristic

 

305

24

October 1956

 

Capacitance

 

306

24

October 1956

 

Quality factor (Q)

 

307

24

October 1956

 

Contact resistance

 

308

29

November 1961

 

Current-noise test for fixed resistors

 

309

27

May 1965

 

Voltage coefficient of resistance determination procedure

310

20

January 1967

 

Contact-chatter monitoring

 

311

14

April 1969

 

Life, low level switching

 

312

16

April 1973

 

Intermediate current switching

 

7

MIL-STD-202G

CLASS 100

ENVIRONMENTAL TESTS

MIL-STD-202G

METHOD 101E

SALT ATMOSPHERE (CORROSION)

(formerly Salt Spray (Corrosion))

1.PURPOSE. The salt-spray test, in which specimens are subjected to a fine mist of salt solution, has several useful purposes when utilized with full recognition of its deficiencies and limitations. Originally proposed as an accelerated laboratory corrosion test simulating the effects of seacoast atmospheres on metals, with or without protective coatings, this test has been erroneously considered by many as an all-purpose accelerated corrosion test, which if "withstood successfully" will guarantee that metals or protective coatings will prove satisfactory under any corrosive condition. Experience has since shown that there is seldom a direct relationship between resistance to salt atmosphere corrosion and resistance to corrosion in other media, even in so-called "marine" atmospheres and seawater. However, some idea of the relative service life and behavior of different samples of the same (or closely related) metals or of protective coating-base metal combinations in marine and exposed seacoast locations can be gained by means of the salt atmosphere test, provided accumulated data from correlated field service tests and laboratory salt atmosphere tests show that such a relationship does exist, as in the case of aluminum alloys. (Such correlation tests are also necessary to show the degree of acceleration, if any, produced by the laboratory test). The salt atmosphere test is generally considered unreliable for comparing the general corrosion resistance of different kinds of metals or coating-metal combinations, or for predicting their comparative service life. The salt atmosphere test has received its widest acceptance as a test for evaluating the uniformity (specifically, thickness and degree of porosity) of protective coatings, metallic and nonmetallic, and has served this purpose with varying amounts of success. In this connection, the test is useful for evaluating different lots of the same product, once some standard level of performance has been established. The salt atmosphere test is especially helpful as a screening test for revealing particularly inferior coatings. When used to check the porosity of metallic coatings, the test is more dependable when applied to coatings that are cathodic rather than anodic toward the basic metal. This test can also be used to detect the presence of free iron contaminating the surface of another metal, by inspection of the corrosion products.

2.APPARATUS. Apparatus used in the salt atmosphere test shall include the following:

a.Exposure chamber with racks or fixtures for supporting specimens.

b.Salt-solution reservoir with means for monitoring an adequate level of solution.

c.Means for atomizing the salt solution, including suitable nozzles and compressed air supply.

d.Chamber-heating means and controls.

e.Means for humidifying the air at a temperature above the chamber temperature.

2.1 Chamber. The chamber and all accessories shall be made of material that will not affect the corrosiveness of the salt atmosphere, such as glass, hard rubber, or plastic. All parts of the test setup that come in contact with test specimens shall be of materials that will not cause electrolytic corrosion. The chamber and accessories shall be so constructed and arranged that there is no direct impinging of the spray or dripping of the condensate on the specimens, so that the atmosphere circulates freely about all specimens to the same degree, and so that no liquid which has come in contact with the test specimens returns to the salt-solution reservoir. The chamber shall be properly vented to prevent pressure build up and allow uniform distribution of salt spray. The chamber shall have a suitable means of heating and maintaining the required test temperature.

2.2 Salt solution reservoir. The salt solution reservoir shall be made of material that is non-reactive with the salt solution, e.g., glass, hard rubber, or plastic. The reservoir shall be adequately protected from the surrounding environment and shall have a means to monitor the solution level. The reservoir shall include a means to filter the salt solution in the supply line to the atomizers. When long duration test conditions are specified (e.g. test condition D), the reservoir may be refilled via auxiliary reservoirs so that the test cycle shall not be interrupted.

METHOD 101E

8 February 2002

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