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rator; Quantitative fit testing using ambient        placed with a high efficiency particulate air
          aerosol as the test agent and appropriate in-        (HEPA) or P100 series filter supplied by the
          strumentation (condensation nuclei counter) to       same manufacturer.
          quantify the respirator fit; Quantitative fit test-
          ing using controlled negative pressure and ap-       (4) The sampling instrument shall be selected
          propriate instrumentation to measure the             so that a computer record or strip chart record
          volumetric leak rate of a facepiece to quantify      may be made of the test showing the rise and
          the respirator fit.                                  fall of the test agent concentration with each
                                                               inspiration and expiration at fit factors of at
            1. General                                         least 2,000. Integrators or computers that inte-
                                                               grate the amount of test agent penetration
          (a) The employer shall ensure that persons ad-       leakage into the respirator for each exercise
          ministering QNFT are able to calibrate equip-        may be used provided a record of the read-
          ment and perform tests properly, recognize           ings is made.
          invalid tests, calculate fit factors properly and
          ensure that test equipment is in proper work-        (5) The combination of substitute air-purifying
          ing order.                                           elements, test agent and test agent concentra-
                                                               tion shall be such that the test subject is not ex-
          (b) The employer shall ensure that QNFT              posed in excess of an established exposure
          equipment is kept clean, and is maintained           limit for the test agent at any time during the
          and calibrated according to the manufacturer’s       testing process, based upon the length of the
          instructions so as to operate at the parameters      exposure and the exposure limit duration.
          for which it was designed.
                                                               (6) The sampling port on the test specimen res-
          2. Generated Aerosol Quantitative Fit Testing        pirator shall be placed and constructed so that
          Protocol                                             no leakage occurs around the port (e.g., where
                                                               the respirator is probed), a free air flow is al-
          (a) Apparatus.                                       lowed into the sampling line at all times, and
                                                               there is no interference with the fit or perfor-
          (1) Instrumentation. Aerosol generation, dilu-       mance of the respirator. The in-mask sampling
          tion, and measurement systems using particu-         device (probe) shall be designed and used so
          lates (corn oil, polyethylene glycol 400 [PEG        that the air sample is drawn from the breath-
          400], di-2-ethyl hexyl sebacate [DEHS] or so-        ing zone of the test subject, midway between
          dium chloride) as test aerosols shall be used        the nose and mouth and with the probe ex-
          for quantitative fit testing.                        tending into the facepiece cavity at least 1/4
                                                               inch.
          (2) Test chamber. The test chamber shall be
          large enough to permit all test subjects to per-     (7) The test setup shall permit the person ad-
          form freely all required exercises without dis-      ministering the test to observe the test subject
          turbing the test agent concentration or the          inside the chamber during the test.
          measurement apparatus. The test chamber
          shall be equipped and constructed so that the        (8) The equipment generating the test atmo-
          test agent is effectively isolated from the ambi-    sphere shall maintain the concentration of test
          ent air, yet uniform in concentration through-       agent constant to within a 10 percent variation
          out the chamber.                                     for the duration of the test.

          (3) When testing air-purifying respirators, the      (9) The time lag (interval between an event
          normal filter or cartridge element shall be re-      and the recording of the event on the strip


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