WAC 296-62-20029
Appendix B -- Industrial hygiene and
medical surveillance guidelines.
APPENDIX B
INDUSTRIAL HYGIENE AND MEDICAL
SURVEILLANCE GUIDELINES
I. INDUSTRIAL HYGIENE GUIDELINES
(1) Sampling. (Benzene-Soluble Fraction Total
Particulate Matter.)
Samples collected should be full shift (8-hour) samples. Sampling should be done using a personal sampling pump
with pulsation damper at a flow rate of 2 liters per
minute. Samples should be collected on 0.8 micrometer
pore size silver membrane filters (37 mm diameter)
preceded by Gelman glass fiber type A filters encased in
three-piece plastic (polystyrene) field monitor
cassettes. The cassette face cap should be on and the
plug removed. The rotameter should be checked every hour
to ensure that proper flow rates are maintained.
A minimum of three full-shift samples should be collected
for each job classification on each battery, at least one
from each shift. If disparate results are obtained for
particular job classification, sampling should be
repeated. It is advisable to sample each shift on more
than one day to account for environmental variables
(wind, precipitation, etc.) which may affect sampling. Differences in exposures among different work shifts may
indicate a need to improve work practices on a particular
shift. Sampling results from different shifts for each
job classification should not be averaged. Multiple
samples from same shift may be used to calculate an
average exposure for a particular job classification.
(2) Analysis.
(a) All extraction glassware is cleaned with dichromic
acid cleaning solution, rinsed with tap water, then
deionized water, acetone, and allowed to dry completely.
The glassware is rinsed with nanograde benzene before
use. The Teflon cups are cleaned with benzene then with
acetone.
(b) Pre-weigh the 2 ml Perkin-Elmer Teflon cups to one
hundredth of a milligram on a Perkin-Elmer autobalance AD
2 Tare weight of the cups is about 50 mg.
(c) Place the silver membrane filter and glass fiber
filter into a 15 ml test tube.
(d) Extract with 5 ml of benzene for five minutes in an
ultrasonic cleaner.
(e) Filter the extract in 15 ml medium glass fritted
funnels.
(f) Rinse test tube and filters with two 1.5 ml aliquots
of benzene and filter through the fritted glass funnel.
(g) Collect the extract and two rinses in a 10 ml Kontes
graduated evaporative concentrator.
(h) Evaporate down to a 1 ml while rinsing the sides with
benzene.
(i) Pipet 0.5 ml into the Teflon cup and evaporate to
dryness in a vacuum oven at 40°C for 3 hours.
(j) Weight the Teflon cup and the weight gain is due to
the benzene soluble residue in half the sample.
II. MEDICAL SURVEILLANCE GUIDELINES
(1) General.
The minimum requirements for the medical examination for
coke oven workers are given in WAC 296-62-20017.
The initial examination is to be provided to all coke
oven workers who work at least thirty days in the
regulated area. The examination includes a 14" x 17"
posterior-anterior chest X ray and a ILO/UC rating to
assure some standardization of X-ray reading, pulmonary
function tests (FVC and FEV 1.0), weight, urinalysis,
skin examination and a urinary cytologic examination. These tests are to serve as the baseline for comparing
the employee's future test results. Periodic exams
include all the elements of the initial exams, except
that the urine cytologic test is to be performed only on
those employees who are forty-five years of age or older
or who have worked for five or more years in the
regulated area; periodic exams, with the exception of X
rays, are to be performed semiannually for this group
instead of annually; for this group, X rays will continue
to be given at least annually. The examination contents
are minimum requirements, additional tests such as
lateral and oblique X rays or additional pulmonary
function tests may be performed if deemed necessary.
(2) Pulmonary function tests.
Pulmonary function tests should be performed in a manner
which minimizes subject and operator bias. There has
been shown to be learning effects with regard to the
results obtained from certain tests, such as FEV 1.0. Best results can be obtained by multiple trials for each
subject. The best of three trials or the average of the
last three of five trials may be used in obtaining
reliable results. The type of equipment used
(manufacturer, model, etc.) should be recorded with the
results as reliability and accuracy varies and such
information may be important in the evaluation of test
results. Care should be exercised to obtain the best
possible testing equipment.
[Statutory Authority: RCW 49.17.010, [49.17].040 and[49.17].050
. 99-17-094, § 296-62-20029, filed 8/17/99,
effective 12/1/99; 98-02-030, § 296-62-20029, filed 12/31/97,
effective 1/31/98; Order 77-14, Appendix B (codified as WAC 296-62-20029), filed 7/25/77.]