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ANSI Z24.22-1957
Pure Tones Anechoic 1 spkr. 34c / 25 / 16 / 12 10 / 8 / 22 10/3 (minimum) Subject fit for best attenuation Yes Random selection, but may choose for good fit if explicitly stated in repoort
ANSI S3.19-1974
1/3-OBa Noise Reverberantb 0.5 s<T60<1.6 s 3 spkrs. min., 1 per plane 24 / 18 / 16 / 16 14 / 9 / 30 10/3 (minimum Subject fit for best atten., or experimenter best fit No Subjects for whom adequate fit cannot be obtained should be noted, but should not be included in the evaluation
ANSI 12.6-1984
1/3-OB noise T60< 1.6 s not specified 28 / 18 / 14 / 14 8 / 9 / 20 10/3 (minimum) Experimenter supervised fit for best attenuation No Subjects for whom good fit cannot be obtained shall be noted, but should not be included in the evaluation
a c
b Reverberation time (T60) - time required for steady-state sound to decay 60 dB. Z24.22 data converted from old to new OBs re ANSI S1.11-1971
should be "randomly" selected, none of the three standards suggests or requires that the test population should be chosen in any particular way that would ensure its representativeness of the target population of users. This is due to the difficulty of defining relevant anatomical selection criteria and of the problems in creating a truly representative sample with a test group of only 10 subjects. All three standards permit exclusion of subjects for whom "adequate" or "good" fits cannot be obtained. This requirement also stems from limitations incurred by using small "representative" test populations. Although S12.6 explicitly requires the laboratory report to include a discussion of any subjects who were dismissed, it is in practice unlikely that such information will be passed on by manufacturers to buyers and end users. Fitting the HPD The most critical aspect of an REAT evaluation is the fitting of the HPD.10 To better define this procedure, S12.6 has eliminated the "subject fit" and "experimenter fit" categories of the previous standard and replaced them with an "experimenter supervised fit." The protectors are put on by the listener and then personally checked by the experimenter who has the option to have the subject refit the HPD "in accordance with the manufacturer's instructions as many times as necessary to obtain a 'best' fit prior to testing but not after the test has begun." A key point of this procedure is that the experimenter is not permitted to actu-
ally fit the protector, but rather must instruct the subject so that the "best" fit is one that is achievable by the subjects themselves. This important restriction arises from the improbability of wearers being inclined to obtain physical assistance in donning their protectors in real-world environments. Another key point pertains to the statement "after the test has begun." Whereas in S3.19 this statement was open to interpretation, S12.6 includes an additional sentence that clearly indicates that once the actual audiometric testing begins no further manipulation of the HPD is permitted. Thus the experimenter cannot use the results of the audiometric testing to assist in determining when the best fit has been obtained. This has been included to try to assure that the "best" fit is indeed one that is potentially achievable in practice without the use of special instrumentation or techniques. However, since the best-fit criterion is intended to yield optimum - performance values regardless of comfort, such values will always represent an upper, and often unobtainable, limit to actual real-world attenuation. Summary ANSI S12.6 should prove to be a more precise standard for the measurement of optimum (laboratory) HPD attenuation than was its predecessor, S3.19. However, it does not address the issue of the noncomparability of laboratory and real-world HPD performance. The principal procedural changes that it embodies are modified hearing protector fitting methods, and incorporation of a specified technique for the reading and
averaging of automatic audiometer traces. A precise determination of the effects these changes will have on attenuation test results awaits implementation of this standard by practicing test laboratories. References and Footnotes
1. ANSI (1957). "Method for the Measurement of Real-Ear Attenuation of Ear Protectors at Threshold," Z24.22-1957 (R1971), NewY ork, NY . 2. ANSI (1974). "Method for the Measurement of Real-Ear Protection of Hearing Protectors and Physical At tenuation of Ear muffs," S3.19-1974 (ASA STD1-1975), NewY ork, NY . 3. ANSI (1984). "Method for the Measurement of Real-Ear Attenuation of Hearing Protectors," S12.6-1984, NewY ork, NY . 4. Berger, E.H. - The EARLog Series is available upon request fromAearoCompany . 5. ANSI S3.19 also included a supplemental section describing the use of a dummy head to measure earmuff attenuation. In S12.6 the decision was made to delete the supplemental test in favor of developing a separate standard specifically for that purpose. 6. Berger, E.H. and Kerivan, J.E. (1983)."Influence of Physiological Noise and the Occlusion Effect on the Measurement of Real-Ear Attenuation at Threshold," J. Acoust. Soc. Am. 74(1), 81-94. 7. Whitham, E.M. and Martin, A.M. (1976).A Review of Methods of Measurement of the Acoustic Attenuation of Hearing Protectors," Inst. of Sound and Vibration Research, Memo No. 528, Southampton, England. 8. Berger, E.H. (1983). "Using the NRR to Estimate the Real WorldPerformanceofHearingProtectors,"SoundandVibration 17(1), 12-18. 9. Martin, A.M. (1979). "Dependence of Acoustic Attenuation of Hearing Protectors on Incident Sound Level," Br. J. Ind. Med. 36,1-14. 10. Berger, E.H. (1983). "Considerations Regarding the Laboratory Measurement of Hearing Protector Attenuation," in Proceedings of Inter-Noise 83, edited by R. Lawrence, Institute of Acoustics, Edinburgh, U.K., 379-382.
EARLog is a registered trademark of Aearo Company. Copyright 1996. First printing 1985
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