Jg. Bennett et al., CORROSIVITY TEST METHODS FOR POLYMERIC MATERIALS .4. CONE CORROSIMETER TEST METHOD, Journal of fire sciences, 12(2), 1994, pp. 175-195
This is the fourth in a series of papers to investigate corrosivity te
st methods published by the Polyolefins Fire Performance Council, an o
perating unit of The Society of the Plastics Industry, Inc. In the fir
st paper, 24 polymeric materials were evaluated for smoke corrosivity
following the test method proposed by ASTM E05.21.70 which uses a radi
ant combustion/exposure apparatus. The second paper discussed the eval
uation of the same materials using the CNET corrosion test method unde
r consideration by ISO TC61/SC4/WG2 and IEC TC89/WG3 and compared the
CNET results with the ASTM E05.21.70 results. In the third paper, the
24 polymeric materials were evaluated using a modified DIN acid gas te
st method and the results were compared to both the previous ASTM E05.
21.70 and CNET results. These commercially available polymeric materia
ls cover a broad range of compositions used for wire and cable insulat
ion and jacketing. In this paper, the same polymeric materials were ev
aluated following the ''Fire Response Standard for Determining the Cor
rosive Effect of Combustion Products Using a Cone Corrosimeter'' propo
sed by ASTM D09.21.04. In this test method, a specimen is subjected to
radiant heat at the recommended heat flux using a spark igniter to ig
nite combustible vapors. A portion of the products of decomposition or
combustion are channeled in a dynamic mode through an exposure chambe
r in which corrosion targets are placed until the specimen has lost 70
% of its total available mass loss. The mass loss is determined from p
revious experiments at the recommended heat flux. When the specimen ha
s lost 70% of its mass loss, the exposure chamber is sealed and isolat
ed. The corrosion of the target is determined by exposing the target t
o the now static combustion products for one hour measured from the st
art of the test. The target is then placed in an environmental chamber
at 75% relative humidity at 23-degrees-C for 24 hours. The test metho
d measures the increase in electrical resistance of a metallic circuit
. This increase is related to the decrease in conductive cross-section
al area resulting from metal loss due to corrosion. The increase in el
ectrical resistance of each target is determined throughout the test a
nd correlated to its metal loss. The 24 hour corrosion value is report
ed as metal loss in angstroms. In this study, heat fluxes of 25 and 50
kW/m2 were used to simulate two different fire scenarios. All of the
materials were run at 50 kW/m2 and 12 materials were run at 25 kW/m2.
Two targets, one with a span of 2,500 angstrom and the second with a s
pan of 45,000 angstrom were used during each test at each heat flux. T
he results of this study indicate that the measured corrosivity of mat
erials: (1) does not correlate consistent with the expectations based
upon the known chemistry of their compositions (2) varies numerically
with the heat flux under which the tests are run and on the target use
d to obtain the corrosion data and (3) although numerically different,
loosely ranks the corrosive potentials of the materials in a consiste
nt manner at both heat fluxes and with both targets. The test protocol
does not specify either the heat flux or the targets to be used recom
mending both in the appendix. As corrosion values are numerically depe
ndent on the conditions and target used to obtain the data, it is ques
tionable how this test method can be used as a standard for determinin
g and comparing the corrosion potentials of materials without requirin
g that both the specific heat flux and the target be specified in the
test protocol as well as be reported with the results. To complete the
review of corrosion test methods, a comparison of the corrosive poten
tials of the 24 materials using the four test methods will be made and
one test method recommended for use as a global standard.