MSC.1/Circ.1312
10 June 2009
REVISED GUIDELINES FOR THE PERFORMANCE AND TESTING CRITERIA, AND
SURVEYS OF FOAM CONCENTRATES FOR FIXED FIRE-EXTINGUISHING SYSTEMS
1 The Maritime
Safety Committee, at its sixtieth session (6 to 10 April 1992), approved Guidelines
for the performance and testing criteria, and surveys of low-expansion foam
concentrates for fixed fire-extinguishing systems (MSC/Circ.582).
2 The Committee, at
its sixty-eighth session (28 May to 6 June 1997), approved Guidelines for the
performance and testing criteria, and surveys of expansion foam concentrates
for fixed fire-extinguishing systems of chemical tankers (MSC/Circ.799).
3 The Sub-Committee
on Fire Protection, at its fifty-third session (16 to 20 February 2009)
reviewed the aforementioned Guidelines and made amendments to the test methods
for both types of foam concentrates which combined the test procedure into one
document.
4 The Committee, at
its eighty-sixth session (27 May to 5 June 2009), after having considered the
above proposal by the Sub-Committee on Fire Protection, at its fifty-third
session, approved the Revised Guidelines for the performance and testing
criteria, and surveys of foam concentrates for fixed fire-extinguishing
systems, as set out in the annex.
5 Member Governments
are invited to apply the annexed Guidelines when approving foam concentrates
for fixed fire-extinguishing systems onboard tankers and chemical tankers and
bring them to the attention of ship designers, shipowners, equipment
manufacturers, test laboratories and other parties concerned.
6 This circular
supersedes MSC/Circ.582 and Corr.1, and MSC/Circ.799. Type approvals conducted
in accordance with the aforementioned Guidelines should remain valid until 1
July 2012.
ANNEX
REVISED GUIDELINES FOR THE PERFORMANCE AND TESTING CRITERIA, AND
SURVEYS OF FOAM CONCENTRATES FOR FIXED FIRE-EXTINGUISHING SYSTEMS
1 GENERAL
1.1 Application
These Guidelines apply to the foam concentrates used for fixed
deck foam fire-extinguishing systems required for tankers by SOLAS regulations
II-2/10.8 and chapter 14 of the International Code for Fire Safety Systems (FSS
Code), and chemical tankers as specified by SOLAS regulation II-2/1.6.2.1.2 and
the International Code for the Construction and Equipment of Ships Carrying
Dangerous Chemicals in Bulk (IBC Code). These Guidelines also apply to foam
concentrates for fixed foam fire-extinguishing systems in machinery spaces
according to chapter 6 of the FSS Code and to portable foam applicators
according to chapter 4 of the FSS Code. These Guidelines do not apply to the
foam generating equipment, only the foam concentrate.
1.2 Definitions
For the purpose of these Guidelines, the following definitions
apply:
1.2.1 Foam (fire
fighting) is an aggregate of air filled bubbles formed from an aqueous
solution of suitable foam concentrate.
1.2.2 Foam solution
is a solution of foam concentrate and water.
1.2.3 Foam concentrate
is a liquid which, when mixed with water in the appropriate concentration,
gives a foam solution.
1.2.4 Expansion ratio
is the ratio of the volume of foam to the volume of foam solution from which it
was made.
1.2.5 Spreading
coefficient is a measurement of the ability of one liquid to spontaneously
spread across another.
1.2.6 25% (50%)
drainage time is the time for 25% (50%) of the liquid content of a foam to
drain out.
1.2.7 Gentle
application is the application of foam to the surface of a liquid fuel via
a backboard, tank wall or surface.
1.2.8 Sediment is
insoluble particles in the foam concentrate.
1.2.9 Aqueous
film-forming foam concentrate (AFF) is a foam concentrate based on a
mixture of hydrocarbon and fluorinated surface active agents.
1.2.10 Alcoholresistant
foam concentrate (AR) is a foam concentrate that is resistant to breakdown
when applied to the surface of alcohol or other polar solvents.
1.2.11 Film-forming
fluoroprotein foam concentrate (FFFP) is a foam concentrate which has the
ability to form an aqueous film on the surface of some hydrocarbons.
1.2.12 Fluoroprotein foam
concentrate (FP) is a protein foam concentrate with added fluorinated
surface active agents.
1.2.13 Protein foam
concentrate (P) is a foam concentrate made from hydrolyzed protein
materials.
1.2.14 Synthetic foam
concentrate (S) is a foam concentrate based on a mixture of hydrocarbon
surface active agents and which may contain fluorocarbons with additional
stabilizers.
1.2.15 Type A foam concentrates
are alcohol-resistant or multi-purpose foam concentrates.
1.2.16 Type B foam
concentrates are all regular type foam concentrates that are not
alcohol-resistant, including fluoroprotein and aqueous film-forming (AFF) foam
concentrates.
2 SAMPLING PROCEDURE
The sampling method should ensure representative samples which
should be stored in filled containers.
The sample size should be:
.1 2 x 20 l containers (or other
standard shipping containers) for type tests (see section 3); and
.2 2 l for periodical controls (see
section 4).
3 TESTS FOR TYPE
APPROVAL OF FOAM CONCENTRATES
For foam concentrate type approval, the tests under paragraphs 3.1
to 3.14 below should be performed by the foam concentrate manufacturer at
laboratories acceptable to the Administration.
3.1 Freezing and
thawing
3.1.1 Before and after
temperature conditioning in accordance with paragraph 3.1.2 below, the foam
concentrate should show no visual sign of stratification, non-homogeneity or
sedimentation.
3.1.2 Freezing and thawing
test:
.1 apparatus:
.1 freezing chamber, capable of achieving
temperatures required, as stated in paragraph 3.1.2.2.1 below;
.2 polyethylene tube, approximately 10 mm
diameter, 400 mm long and sealed and weighted at one end, with suitable spacers
attached. Figure 1 shows a typical form; and
.3 500 ml cylinder, approximately 400 mm high
and 65 mm in diameter.
.2 procedure:
.1 set the temperature of the freezing
chamber to a temperature which is 10C below the freezing point of the sample
measured in accordance with standard BS 5117, section 1.3 (excluding 5.2 in the
standard). To prevent the glass measuring cylinder from breaking, due to
expansion of the foam concentrate on freezing, insert the tube into the
measuring cylinder, sealed end downward, weighted if necessary to avoid
flotation, and the spacers ensuring it remains approximately on the central
axis of the cylinder. Place the cylinder with the sample in the chest, cool it
and maintain at the required temperature for 24 h. At the end of this period,
thaw the sample for not less than 24 h and not more than 96 h in an ambient
temperature of 20 to 25C;
.2 repeat the procedure described in the
above subparagraph three times to give four cycles of freezing and thawing; and
.3 condition the sample for seven days at
60C followed by one day at room temperature. The sample shall then be examined
for visual signs of stratification, non-homogeneity or sedimentation.
3.2 Heat stability
An unopened 20 l container (or other standard shipping
container), as supplied by the manufacturer from a production batch, should be
maintained for seven days at 60C, followed by one day at room temperature.
Following this conditioning, the foam liquid after agitating/stirring will be
subjected to the fire test as per subsection 3.9. Only fire tests as per
subsection 3.9 should be performed with the heat conditioned sample.
3.3 Sedimentation
3.3.1 Any sediment in the
concentrate prepared in accordance with section 2 should be dispersible through
a 180 m sieve, and the percentage volume of sediment should not be more than
0.25% when tested in accordance with paragraph 3.3.2 below.
3.3.2 The test should be
carried out as follows:
.1 apparatus:
.1 graduated centrifuge tubes;
.2 centrifuge operating at 6,000 100 m/s2;
.3 180 m sieve complying with standard ISO
3310-1; and
.4 plastic wash bottle.
Note:
a centrifuge and tubes complying with standard ISO 3734 are
suitable; and
.2 procedure: centrifuge each sample for 10
min. Determine the volume of the sediment and determine the percentage of this
volume with respect to the centrifuged sample volume. Wash the contents of the
centrifuge tube onto the sieve and check that the sediment can or cannot be
dispersed through the sieve by the jet from the plastic wash bottle.
Note: It is possible
that the test method is not suitable for some non-Newtonian foam concentrates.
In this case an alternative method, to the satisfaction of the Administration,
should be used so that compliance with this requirement can be verified.
3.4 Kinematic viscosity
3.4.1 The test should be
carried out according to standard ASTM D 445-86 or ISO 3104. Kinematic
viscosity should not exceed 200 mm2/s.
3.4.2 The method for
determining viscosity of non-Newtonian foam concentrates or kinematic viscosity
exceeding 200 mm2/s should be to the satisfaction of the
Administration. A suitable method is described in standard EN 1568.
3.5 pH value
The pH of the foam concentrate prepared in accordance with section
2 should be not less than 6 and not more than 9.5 at 20 2C.
3.6 Film formation of
the foam solution (if applicable)
3.6.1 The spreading
coefficient should be determined using the following formula:
S = Tc Ts - Ti
where:
S is the spreading
coefficient;
Tc is the surface tension of cyclohexane (N/m);
Ts is the surface tension of the foam
solution (N/m);
Ti is
the interfacial tension between the foam solution and cyclohexane (N/m).
Tc, Ts and Ti
should be determined according to paragraph 3.6.2 below.
The spreading coefficient S should be greater than 0.
3.6.2 Determination of
Tc, Ts and Ti
.1 materials:
.1 solution of foam
concentrate, at the recommended usage concentration in distilled water
complying with standard ISO 3696; and
Note:
The solution may be made up in a 100 ml volumetric flask
using a pipette to measure the foam concentrate.
.2 for Tc
and Ti, cyclohexane of purity not less
than 99%;
.2 procedures for surface tension: determine
Ts at a temperature of 20 2C using the ring or plate
method of standard ISO 304; and
.3 procedure for interfacial tension: after
measuring the surface tension in accordance with subparagraph .2 above,
introduce a layer of cyclohexane at 20 2C onto the foam solution, being
careful to avoid contact between the ring or plate and the cyclohexane. Wait 6
1 min and measure Ti.
3.7 Expansion ratio
3.7.1 The test should be
carried out according to paragraph 3.7.2 with simulated seawater at about 20C
having the characteristics stated in paragraph 3.7.3.
3.7.2 Determination of
the expansion ratio
.1 apparatus:
.1 plastic collecting vessel of volume V,
known to 16 ml, as shown in figure 2, equipped with a bottom discharge
facility;
.2 foam collector, as shown in figure 3; and
.3 foam making equipment with nozzle, as
shown in figure 4, which when tested with water has a flow rate of 11.4 l/min
at a nozzle pressure of 6.3 0.3 bar;
.2 procedure:
.1 check that the pipe work and hose from the
foam solution tank to the nozzle is completely full of solution. Set up the
nozzle horizontally directly in front of the foam collector with the front of
the nozzle 3 0.3 m from the top edge of the collector. Wet the vessel
internally and weigh it (W1). Set up the foam equipment and
adjust the nozzle pressure to give a flow rate of 11.4 l/min. Discharge
the foam and adjust the height of the nozzle so that the discharge strikes the
collector centrally. Keep the nozzle horizontal. Stop the foam discharge and
rinse all foam from the collector. Check that the foam solution tank is full.
Start discharging the foam and after 30 5 s to allow the discharge to
stabilize, place the collecting vessel, with the discharge outlet closed, on
the collector. As soon as the vessel is full, remove it from the collector,
strike the foam surface level with the rim and start the clock. Weigh the
vessel (W2);
.2 calculate the expansion E from the
equation:
E
=
V / (W2 W1)
in
which it is assumed that the density of the foam solution is 1 and where:
V is the vessel volume in ml;
W1 is the mass of the empty vessel in
grams;
W2 is the mass of the full vessel in grams;
and
.3 open the drainage facility and collect the
foam solution in the measuring cylinder to measure the 25% drainage time (see
paragraph 3.8.1 below).
3.7.3 Simulated sea water
may be made up by dissolving in 0.9584 kg of potable water:
25 g Sodium
chloride (NaCl);
11 g Magnesium
chloride (MgCl2
6 H2O);
1.6 g Calcium
chloride (CaCl2
2H2O);
4 g Sodium
sulphate (Na2
SO4).
3.8 Drainage time
3.8.1 The drainage time
should be determined according to paragraph 3.7.2.3 above, after having determined
the expansion ratio.
3.8.2 The test should be
carried out with simulated seawater at about 20C having the characteristics
stated in paragraph 3.7.3 above.
3.9 Fire tests
Fire tests should be carried out according to paragraphs 3.9.1 to
3.9.7.
Note: The fire tests of this subsection 3.9 are more expensive and time
consuming than the other tests of these Guidelines. It is recommended that fire
tests should be carried out at the end of the test programme, so as to avoid
the expense of unnecessary testing of foam concentrates which do not comply in
other respects.
3.9.1 Environmental conditions:
.1 air temperature 15 5C;
.2 fuel temperature 17.5 2.5C;
.3 water temperature 17.5 2.5C;
.4 foam solution temperature 17.5 2.5C; and
.5 maximum wind speed 3 m/s in proximity of
the fire tray.
Note: If necessary, some form of wind-screen may be used.
3.9.2 Observations
during the fire test:
During the fire test, record the following:
.1 indoor or outdoor test;
.2 air temperature;
.3 fuel temperature;
.4 water temperature;
.5 foam solution temperature;
.6 wind speed;
.7 extinction time; and
.8 25% burnback time.
Note: Burnback time may either be determined visually by an experienced
person or may be determined from thermal radiation measurements (a suitable
method is described in standard EN 1568).
3.9.3 Foam solution:
.1 prepare a foam solution following the
recommendations from the supplier for concentration, maximum premix time,
compatibility with the test equipment, avoiding contamination by other types of
foam, etc; and
.2 the test should be carried out with
simulated sea water at about 20C having the characteristics stated in
paragraph 3.7.3 above.
3.9.4 Apparatus:
.1 fire tray: square tray with the following
dimensions:
area 4.5
m2;
depth 200
mm;
thickness of
steel wall 2.5 mm;
with a vertical
steel backboard 1 0.05 m high and 1 0.05 m long;
.2 foam making equipment: in accordance with
paragraph 3.7.2.1 for type B foam concentrates. For type A foam concentrates,
the foam application rate should be as determined by the manufacturer, up to a
total of three nozzles in accordance with paragraph 3.7.2.1;
.3 burnback pot: circular burnback pot with
the following dimensions:
diameter 300 5
mm;
height 150
5 mm;
thickness of
steel wall 2.5 mm.
3.9.5 Fuel
3.9.5.1 For type B foams,
use an aliphatic hydrocarbon mixture with physical properties according to the
following specification:
distillation
range 84C
to 105C;
maximum
difference between initial and
final
boiling points 10C;
maximum
aromatic content 1%;
density
at 15C 707.5
2.5 kg/m3;
temperature
about 20C.
Note: Typical fuels meeting this specification are n-heptane and certain
solvent fractions sometimes referred to as commercial heptane.
The Administration may require additional fire tests using an
additional test fuel.
3.9.5.2 For type A foams,
acetone and isopropyl alcohol should be used as the standard test fuels.
However, the Administration may require additional fire tests using different
test fuels for water-miscible cargoes that require a higher foam application
rate than acetone. Impurities for all type A fuels should not exceed 1%.
3.9.6 Test procedure:
.1
place the tray directly on the ground and ensure that it is level. If using
heptane, add approximately 90 l of simulated sea water having the
characteristics stated in paragraph 3.7.3, and check that the base of the tray
is completely covered. Set up the foam nozzle horizontally, about 1 m above the
ground in a position where the central part of the foam discharge will strike
the centre axis of the backboard, 0.35 0.1 m above the rim of the tray
(gentle application). Add 144 5 l of fuel, to give a nominal freeboard
of 150 mm. If using acetone or isopropyl alcohol, add 234 5 l of fuel
directly into the tray, without water, to give a nominal freeboard of 150 mm;
.2 ignite the tray not more than 5 min after
adding the fuel and allow it to burn for a period of 60 5 s after full
involvement of the surface of the fuel, then start foam application; and
.3 apply foam for 300 2 s. Stop foam
application and after a further 300 10 s place the burnback pot, containing 2
0.1 l of fuel in the centre of the tray and ignite. Visually estimate
when 25% of the tray is covered by sustained flames or by flare up flames
(see Note below), ignoring any faint, barely visible, or transient flames.
Note: During the burnback test, a flare up may occur, in which large
flames may be sustained for periods typically from 30 s to 3 min before
decreasing in intensity.
3.9.7 Permissible
limits:
.1 extinction time: not more than 5 min; and
.2 burnback time: not less than 15 min for
25% of the surface.
3.10 Corrosiveness
The storage container should be compatible with its foam
concentrate throughout the service life of the foam such that the chemical and
physical properties of the foam should not deteriorate below the initial values
accepted by the Administration.
3.11 Volumic mass
According to standard ASTM D 1298-85.
3.12 Batch certificate
The foam concentrate should be delivered with a declaration of the
main characteristics (sedimentation, pH value, expansion ratio, drainage time
and volumetric mass). The declaration should be issued by the maker and will be
the basis for the annual condition test.
3.13 Foam concentrate
container marking
Each foam concentrate container should be marked with complete
information needed to identify the liquid and confirm its intended use. As a
minimum, the following information should be included:
.1 name and address of manufacturer;
.2 product designation;
.3 type of foam (synthetic, protein-based,
etc.);
.4 intended use (regular or
alcohol-resistant);
.5 batch number and reference to batch
certificate;
.6 date of manufacture;
.7 expiry date;
.8 reference to test standard and approvals;
.9 recommended usage concentration;
.10 indication if seawater compatible;
.11 maximum and minimum storage temperature;
.12 required onboard storage tank materials
(steel, stainless steel, FRP, etc.);
.13 quantity of foam concentrate;