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Evaluation of pump pulsation in respirable size-selective sampling: part III. Investigation of European standard methods.

Authors
Soo-J-C; Lee-EG; Lee-LA; Kashon-ML; Harper-M
Source
Ann Occup Hyg 2014 Oct; 58(8):1006-1017
NIOSHTIC No.
20044739
Abstract
Lee et al. (Evaluation of pump pulsation in respirable size-selective sampling: part I. Pulsation measurements. Ann Occup Hyg 2014a;58:60-73) introduced an approach to measure pump pulsation (PP) using a real-world sampling train, while the European Standards (EN) (EN 1232-1997 and EN 12919- 1999) suggest measuring PP using a resistor in place of the sampler. The goal of this study is to characterize PP according to both EN methods and to determine the relationship of PP between the published method (Lee et al., 2014a) and the EN methods. Additional test parameters were investigated to determine whether the test conditions suggested by the EN methods were appropriate for measuring pulsations. Experiments were conducted using a factorial combination of personal sampling pumps (six medium- and two high-volumetric flow rate pumps), back pressures (six medium- and seven high-flow rate pumps), resistors (two types), tubing lengths between a pump and resistor (60 and 90 cm), and different flow rates (2 and 2.5 l min-1 for the medium- and 4.4, 10, and 11.2 l min-1 for the high-flow rate pumps). The selection of sampling pumps and the ranges of back pressure were based on measurements obtained in the previous study (Lee et al., 2014a). Among six medium-flow rate pumps, only the Gilian5000 and the Apex IS conformed to the 10% criterion specified in EN 1232-1997. Although the AirChek XR5000 exceeded the 10% limit, the average PP (10.9%) was close to the criterion. One high-flow rate pump, the Legacy (PP = 8.1%), conformed to the 10% criterion in EN 12919-1999, while the Elite12 did not (PP = 18.3%). Conducting supplemental tests with additional test parameters beyond those used in the two subject EN standards did not strengthen the characterization of PPs. For the selected test conditions, a linear regression model [PPEN = 0.014 + 0.375 PPNIOSH (adjusted R2 = 0.871)] was developed to determine the PP relationship between the published method (Lee et al., 2014a) and the EN methods. The 25% PP criterion recommended by Lee et al. (2014a), average value derived from repetitive measurements, corresponds to 11% PPEN. The 10% pass/fail criterion in the EN Standards is not based on extensive laboratory evaluation and would unreasonably exclude at least one pump (i.e. AirChek XR5000 in this study) and, therefore, the more accurate criterion of average 11% from repetitive measurements should be substituted. This study suggests that users can measure PP using either a real-world sampling train or a resistor setup and obtain equivalent findings by applying the model herein derived. The findings of this study will be delivered to the consensus committees to be considered when those standards, including the EN 1232-1997, EN 12919-1999, and ISO 13137-2013, are revised.
Keywords
Sampling; Samplers; Respiration; Pumps; Particulates; Particulate-sampling-methods; Aerosols; Aerosol-particles; Author Keywords: amplitude; frequency; penetration shift; pulsation magnitude; pump pulsation; respirable cyclones; sampling efficiency
Contact
Eun Gyung Lee, Exposure Assessment Branch (EAB), Health Effects Laboratory Division (HELD), National Institute for Occupational Safety and Health (NIOSH), 1095 Willowdale Road, Morgantown, WV 26505
CODEN
AOHYA3
Publication Date
20141001
Document Type
Journal Article
Email Address
dtq5@cdc.gov
Fiscal Year
2015
NTIS Accession No.
NTIS Price
Identifying No.
M072014
Issue of Publication
8
ISSN
0003-4878
NIOSH Division
HELD
Priority Area
Mining
Source Name
Annals of Occupational Hygiene
State
WV
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