GSO ISO 16107:2008
ISO 16107:1999
Gulf Standard
Current Edition
·
Approved on
20 February 2008
Workplace atmospheres-Protocol for evaluating the performance of diffusive samplers
GSO ISO 16107:2008 Files
English
15 Pages
Current Edition
Reference Language
OMR
46.16
GSO ISO 16107:2008 Scope
1 Scope
1.1 This International Standard covers the evaluation of the performance of diffusive samplers of gases and
vapours for use over sampling periods from 4 h to 12 h. Sampling periods of such duration are the most common in
workplace sampling. Given a suitable exposure chamber, this International Standard can be straightforwardly
extended to cover samplers for use over other sampling periods as well. The aim is to provide a concise set of
experiments for classifying samplers primarily according to a single numerical value representing sampler accuracy.
NOTE Accuracy estimates refer to conditions of sampler use which are normally expected in a workplace setting. These
conditions may be characterized by the temperature, atmospheric pressure, humidity and ambient wind speed, none of which
may be constant or accurately known. Furthermore, the accuracy accounts for difficulty in the estimation of time-weighted
averages of concentrations which may not be constant in time.
In addition to accuracy determination, a method is provided to test the samplers for compliance with the
manufacturer's stated limits on capacity, possibly in the presence of interfering compounds. A method is given for
classification of samplers according to their capability to detect situations in which sampler capacity may be
exceeded.
1.2 This International Standard is an extension of previous research on diffusive samplers [1-17] as well as EN
838. Essential advantages are the estimation of sampler accuracy under actual conditions of use and the reduction
in cost of sampler evaluation.
NOTE Furthering the latter point, knowledge of similarity between analytes of interest can be used to expedite sampler
evaluation. For example, interpolation of data characterizing the sampling of analytes at separated points of a homologous
series of compounds is recommended. At present the procedure in [9] is suggested: Following evaluation of a sampler in use at
a single homologous series member according to the present practice, higher molecular weight members would receive partial
validations considering sampling rate, capacity, analytical recovery and interferences.
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