Значение и использование

Although a cleaning action is imparted to the test component, it is not the intent of this practice to serve as a cleaning procedure. Components are normally cleaner after each consecutive test; thus repeated tests may be used to establish process limits for a given component (Fig. 4). A specific set of test parameters must be supplied by the agency specifying cleanliness limits. Fig. 1, Fig. 2, and Fig. 3 may be used as a guide to establish the desired parameters of test fluid, vibration, extraction, and analysis.

The curve in Fig. 4 shows the typical behavior of a component when tested for cleanliness several consecutive times. Stabilization generally occurs before the fifth successive run. The stabilized region starts where a horizontal line through the maximum stabilized value intersects the curve.

The allowable cleanliness limit of a test component should be based on the cleanliness requirements of the system in which it will be used and the assigned value should be greater than the maximum stabilized value. When defining the allowable cleanliness limits, an important consideration is that the accuracy of the results decreases as the allowable limit value approaches the stabilized value.

FIG. 4 Contamination per Test Run Versus Consecutive Test Run Number

Область применения

1.1 These practices cover sampling procedures for use in determining the particle cleanliness of liquids and liquid samples from components. Three practices, A, B, and C, have been developed on the basis of component geometry in order to encompass the wide variety of configurations. These practices establish guidelines to be used in preparing detailed procedures for sampling specific components.

Note 1—The term cleanliness used in these practices refers to solid particles in the liquid. It does not generally cover other foreign matter such as gases, liquids, and products of chemical degradation. Cleanliness with respect to particulate contamination does not necessarily give any indication of the other types of contamination.

1.2 All components, regardless of application, may be tested provided (1) the fluid medium selected is completely compatible with the materials, packing and fluid used in the test component, and test apparatus, and (2) the fluid is handled in accordance with the manufacturer's recommendations and precautions. A liquid shall be used as the test fluid medium. These test fluids may be flushing, rinsing, packing, end use operating, or suitable substitutes for end use operating fluids. (Warning—Practices for sampling surface cleanliness by the vacuum cleaner technique (used on clean room garments and large storage tanks) sampling gaseous fluids and handling hazardous fluids such as oxidizers, acids, propellants, and so forth, are not within the scope of the practices presented; however, they may be included in addendums or separate practices at a later date.

Substitute fluids are recommended in place of end item fluids for preassembly cleanliness determinations on components using hazardous end item fluids. After obtaining the sample, the substitute fluid must be totally removed from the test part with particular caution given to the possibility of trapped fluid. It is hazardous to use a substitute fluid for testing assembled parts where the fluid can be trapped in dead ends, behind seals, and so forth.)

Note 2—The word fluid used in these practices shall be assumed to be a liquid unless otherwise stated.

1.3 The cleanliness of assemblies with or without moving parts may be determined at the time of test; however, movement of internal component parts during the test will create unknown quantities of contamination from wear. Practice B covers configurations requiring dynamic actuation to achieve a sample. The practice does not differentiate between built-in particles and wear particles.

Note 3—Defining allowable cleanliness limits is not within the scope of these practices.

1.4 The three practices included are as follows:

Sections Practice A—Static Fluid Sampling (Method for extracting fluid from the test article for analysis. This applies to components that have a cavity from which fluid may be extracted) 5-13 Practice B—Flowing Fluid Sampling (Method for flushing contaminants from the test article for analysis. This applies to components which fluid can pass (1) directly through, or (2) pass into and out of by cycling)14-22 Practice C—Rinse Fluid Sampling (Method for rinsing contaminants from the test article's surfaces. The rinse fluid is analyzed for contamination. This applies to components that do not have a fluid cavity or for other reasons are not adaptable to Practices A and B)23-31

1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.