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Patty's Industrial Hygiene, Physical and Biological Agents


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which had been calibrated in New Zealand in summer under high solar UV conditions, showed deviations of up to 30%, compared to the erythemally weighted irradiance determined from reference spectroradiometer measurements, when tested in northern Germany in autumn (40).

      4.3 Alternative Assessment Methods

      Alternatives to direct measurement of optical radiation may be needed when reliable measurement instruments are not available or when installation of a source is being planned or designed. Alternative methods include calculations of radiometric values and use of lamp classifications. Other source‐related guidelines, such as the UV Index (UVI) for solar radiation and shade numbers for welding, are discussed in Section 6.

      4.3.1 Calculation of Effective Radiometric Values

      If the source data are reported in terms of spectral irradiance, the manufacturer should provide information on the geometric configuration at which the spectral irradiance was measured. If the measurement distance exceeded five times the longest dimension of the source, then the following version of the inverse square law can be used to calculate the effective irradiance at the exposed surface of the skin or eye, Esurf:

      where rsurf is the distance between the source and the exposed body surface, Eref is the effective radiance under the measurement conditions, and rref is the measurement distance.

Hazard Exempt Group RG‐1 very low risk RG‐2 low risk RG‐3 high risk
Exposure limit will not be exceeded within a period of
Actinic UV hazard 8 h 10 000 s 1000 s Fails RG‐2 criterion
UV‐A hazard 1000 s 300 s 100 s Fails RG‐2 criterion
IR‐cornea/lens hazard 1000 s 100 s 10 s Fails RG‐2 criterion
Retinal thermal hazard (arc sources) 0.25 s n/a n/a Fails Exempt Group criterion
Blue‐light hazard 10 000 s 100 s 0.25 s Fails RG‐2 criterion
IR‐retinal hazard, non‐lighting sources 810 s 10 s n/a Fails RG‐1 criterion

      h, hour; s, second.

      4.3.2 Lamp Classifications

      Radiation‐emitting devices, including optical radiation sources, are subject to regulation in the United States by the U.S. Food and Drug Administration (FDA) through its Center for Devices and Radiological Health. The FDA has not established a classification system, analogous to its laser classification system, for noncoherent optical radiation sources.

      In the absence of governmental regulations requiring safety‐related classification of all lamps, the IESNA has published a voluntary guideline, ANSI/IES RP‐27.3, Recommended Practice for Photobiological Safety for Lamps and Lamps SystemsRisk Group Classification and Labeling (44). This recommended practice applies to all electrically powered sources emitting radiation between 200 and 3000 nm, except for LEDs used in fiber optic communications systems and lasers. Laser‐driven broadband light sources are included under the standard.