Appendix – Fire Test Procedures for Non-Combustibility
Test
Introduction
This fire test is for identification of products which produce
only a very limited amount of heat and flame when exposed to temperatures
of approximately 750°C.
Safety Warning
The attention of all persons concerned with managing and
carrying out this test is drawn to the fact that fire testing may
be hazardous and that there is a possibility that toxic and/or harmful
smoke and gases may be evolved during the test. Operational hazards
may also arise during the testing of specimens and the disposal of
test residues.
An assessment of all potential hazards and risks to health
shall be made and safety precautions shall be identified and provided.
Written safety instructions shall be issued. Appropriate training
shall be given to relevant personnel. Laboratory personnel shall ensure
that they follow written safety instructions at all times.
1 Scope
1.1 This appendix specifies test procedures for
determining the non-combustibility.
1.2 Information on the precision of the test method
is given in annex A of standard ISO 1182.
2 Normative References
The following normative documents contain provisions which
constitute provisions of this appendix.
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.1 ISO 1182, Reaction to fire tests for building
and transport products – Non-combustibility test; and
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.2 ISO 13943, Fire safety – Vocabulary.
3 Terms and Definitions
For the purpose of this appendix, the terms and definitions
given in Fire safety – Vocabulary (ISO 13943), together with
the following, apply:
3.1
Homogeneous product is a product,
consisting of a single material, having uniform density and composition
throughout the product.
3.2
Loose fill material is a material
without any physical shape.
3.3
Material is a single basic substance
or uniformly dispersed mixture of substances, e.g., metal, stone,
timber, concrete, mineral wool with uniformly dispersed binder, polymers.
3.4
Non-homogeneous product is a
product that does not satisfy the requirements of a homogeneous product.
It is a product composed of more than one component, substantial and/or
non-substantial.
3.5
Product is material, element
or component about which information is required.
3.6
Sustained flaming shall be taken
as the persistence of flames on, or over any part of, the visible
part of the specimen lasting 5 s or longer.
3.7 Moisture content
3.7.1 The specimen for determining the moisture
content and organic contents shall not be used for the non-combustibility
test.
3.7.2 The moisture content (W1-W2)
of each specimen shall be calculated using the following method, and
indicate a percentage of the dry weight (W2), and which
information is required.
3.7.3 In the following, W1, W2 and
W3 are mean values of three weight measurements. W1 shall
be higher than 25 g. Three specimens of each material, taken in the
width of the production's direction and measuring width x minimum
20 mm x thickness of the material, shall be weighed (initial conditioned
weight W1) and then heated in a ventilated oven at a temperature
of 105 ± 2°C for 24 h and reweighed when cooled (W2).
However, gypsum-based, cementations and similar materials shall be
dried at a temperature of 55 ± 5°C to constant weight (W2).
3.7.4 The moisture content (W1-W2)
of each specimen shall be calculated as a percentage of the dry weight
(W2).
3.8 Organic content
3.8.1 The information of organic content is required.
After the percentage moisture contents have been calculated as specified
above, the three specimens shall be further heated in an oven at a
temperature of 500 ± 20°C for 2 h and again weighed (W3).
The organic content (W2-W3) shall be calculated
as a percentage of the dry weight (W2).
3.8.2 The organic content of each material used
in the test specimen shall be within ± 0.3% absolute of the
value stated as the nominal organic content.
4 Test Apparatus
The test apparatus including thermocouples, specimen holders
and other necessary peripherals shall be in accordance with Reaction
to fire tests for building and transport products – Non-combustibility
test (ISO 1182). Calibration of the test apparatus shall be conducted
in accordance with the ISO standard.
5 Test Specimen
5.1 General
5.1.1 The test specimen shall be taken from a
sample which is sufficiently large to be representative of the product.
5.1.2 The test specimens shall be cylindrical
and each shall have a diameter of 43 mm to 45 mm and a height of 50
± 3 mm.
5.2 Preparation
5.2.1 If the thickness of the material is different
from 50 ± 3 mm, specimens of the height of 50 ± 3 mm
shall be made by using a sufficient number of layers of the material
and/or by adjustment of the material thickness.
5.2.2 For non-homogeneous materials, the specimen
of height of 50 ± 3 mm shall be constructed such that all layers
are represented in the specimen in proportion to their presence, by
volume, in the original specimen.
5.2.3 The layers shall occupy a horizontal position
in the specimen holder and shall be held together firmly, without
significant compression, by means of two fine steel wires, of maximum
diameter 0.5 mm, to prevent air gaps between layers. The specimens
of loose fill materials shall be representative in appearance, density,
etc., as in use.
5.3 Number
For homogeneous products, five specimens shall be made.
For non-homogeneous products, 10 specimens shall be made.
6 Conditioning
The test specimens shall be dried in a ventilated oven maintained
at 60 ± 5°C, for between 20 h and 24 h, and cooled to ambient
temperature in a desiccator prior to testing. The mass of each specimen
shall be determined to an accuracy of 0.01 g prior to test.
7 Test Procedure
7.1 Test environment
The apparatus shall not be exposed to draughts or any form
of strong direct sunlight or artificial illumination which would adversely
affect the observation of flaming inside the furnace. The room temperature
shall not change by more than 5°C during a test.
7.2 Setting up procedure
Remove the specimen holder and its support from the furnace.
7.2.2.1 Furnace thermocouple
The furnace thermocouple shall be located with its hot junction
10 ± 0.5 mm from the furnace tube wall and at a height corresponding
to the geometric centre of the furnace tube.
7.2.2.2 Specimen surface thermocouple
The specimen surface thermocouple shall be positioned so
that its hot junction is in contact with the specimen at mid-height
of the specimen at the start of the test and shall be located diametrically
opposite the furnace thermocouple.
Connect the heating element of the furnace either to the
voltage stabilizer, variable transformer and the electrical input
monitor or the power controller. Automatic thermostatic control of
the furnace shall not be used during testing.
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Note 1 : The heating element should normally draw
a current of between 9 A and 10 A at approximately 100 V under steady
state conditions. In order not to overload the winding, it is recommended
that the maximum current does not exceed 11 A.
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Note 2: A new furnace tube should be subjected
to slow heating initially. A suitable procedure has been found to
be to increase the furnace temperature in steps of approximately 200°C,
allowing 2 h heating at each temperature.
7.2.4
Furnace stabilization
Adjust the power input to the furnace so that the average
furnace temperature, as indicated by the furnace thermocouple, is
stabilized for at least 10 min at 750 ± 5°C. The drift
(linear regression) shall not be more than 2°C during these 10
min and there shall be a maximum deviation from the average temperature
of not more than 10°C in 10 min.
7.3 Standard test procedure
7.3.1 Stabilize the furnace as described in paragraph
7.2.4. If the recorder used does not allow a real-time calculation,
the temperature stabilization shall be checked afterwards. If the
conditions specified in paragraph 7.2.4 were not satisfied, the test
shall be repeated.
7.3.2 Before starting the test, ascertain that
the whole equipment is in good working order, for example, that the
stabilizer is clean, the specimen insertion device is working smoothly
and the specimen holder exactly occupies the required position in
the furnace.
7.3.3 Insert one specimen prepared and conditioned
as specified in paragraph 6 into the specimen holder suspended on
its support.
7.3.4 Place the specimen holder in the furnace
in the position taking not more than 5 s for this operation. The position
of the specimen shall be such that the geometric centre of the specimen
is located rigidly at the geometric centre of the furnace during the
test.
7.3.5 Start observation of flaming before the
specimen is lowered into the furnace.
7.3.6 Start the timing device immediately following
the insertion of the specimen into the furnace.
7.3.7 Record in intervals not longer than 1 s,
throughout the test, the temperature measured by the furnace thermocouple
and the specimen surface thermocouple.
7.3.8 Carry out the test for a period of 30 min.
7.3.9 After cooling the specimen to ambient temperature
in a desiccator, weigh the specimen. Recover any char, ash or other
debris which breaks off the specimen and falls down the tube, either
during or following the test, and include this as a part of the unconsumed
specimen.
7.3.10 For homogeneous products, test five specimens
as described in paragraphs 7.3.1 to 7.3.9.
7.3.11 For non-homogeneous products, test five
specimens oriented with one surface on the top of the test specimen
as described in paragraphs 7.3.1 to 7.3.9. Repeat with the remaining
five specimens oriented with that surface on the bottom.
7.4 Observations during test
7.4.1 Record the mass, in g, before and after
the test for each specimen tested according to paragraph 7.3, and
note any observations relating to the behaviour of the specimen during
the test including during insertion into the apparatus.
7.4.2 Note the occurrence of any sustained flaming
and record the duration of such flaming in seconds.
7.4.3 Record the following temperatures, in °C,
as measured by the thermocouples:
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.1 the initial furnace temperature, Ti(furnace)
which is the average temperature over the final 10 min
of the stabilization period as defined in paragraph 7.2.4;
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.2 the maximum furnace temperature Tm(furnace)
and the maximum specimen surface temperature Tm(surface)
, which are the discrete values at maximum temperature
anywhere over the entire test period; and
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.3 the final furnace temperature Tf(furnace)
and the final specimen surface temperature Tf(surface)
, which is the average temperature over the final 1 min
of the test period as defined in paragraph 7.3.8.
8 Expression of Results
8.1 Calculation of averages
8.1.1 For homogeneous products, calculate the
averages for paragraphs 8.2 (Mass loss) to 8.5 (Average temperature
rise) for the five specimens.
8.1.2 For non-homogeneous products, calculate
the averages for paragraphs 8.2 (Mass loss) to 8.5 (Average temperature
rise) for each set of five specimens in the same orientation. The
results for each orientation shall be presented separately, but they
shall not be combined. Classification shall be based on the most onerous
orientation such that all the averages for each set of five specimens
shall meet the requirements in paragraph 3 of part 1.
8.2 Mass loss
8.2.1 Calculate and record the mass loss in percentage
for each of the five specimens, expressed as a percentage of the initial
mass of the specimen, measured as specified in paragraph 7.4.1.
8.2.2 Calculate the average mass loss in percentage,
which is the average of mass loss of the five specimens.
8.3 Flaming
8.3.1 Calculate and record the total duration
of sustained flaming, in seconds, for each of the five specimens measured
as specified in paragraph 7.4.2.
8.3.2 Calculate the average duration of sustained
flaming, which is the average of total duration of sustained flaming
of the five specimens.
8.4 Temperature rise
Calculate and record the following temperature rise in °C
for each of the five specimens recorded by the thermocouples as specified
in paragraph 7.4.3
8.5 Average temperature rise
Calculate the average furnace temperature rise Tave
r(furnace)
and the average specimen surface temperature
rise Tave r(surface)
from the values obtained
by paragraph 8.4.
9 Test Report
The test report shall include the following information
as a minimum. A clear distinction shall be made between the data provided
by the sponsor and data determined by the test:
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.1 reference that the test was carried out in
accordance with part 1 of the 2010 FTP Code (see also subparagraph
.2);
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.2 any deviations from the test method;
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.3 name and address of the testing laboratory;
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.4 date and identification number of the report;
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.5 name and address of the sponsor;
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.6 name and address of the manufacturer/supplier,
if known;
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.7 name and/or identification of the product tested;
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.8 description of the sampling procedure, where
relevant;
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.9 description of the product tested including
density, mass per unit area and thickness, together with details of
the construction, moisture content and organic content of the product;
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.10 description of the specimen including dimensions,
orientations and construction;
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.11 date of sample arrival;
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.12 details of specimen conditioning;
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.13 date of test;
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.14 test results expressed in accordance with
paragraph 8;
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.15 observations made during the test;
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.16 classification of the material; and
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.17 the statement:
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"The test results relate to the behaviour of the test specimens
of a product under the particular conditions of the test; they are
not intended to be the sole criterion for assessing the potential
fire hazard of the product in use.".
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