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Iso 7203-2-2019
Iso 7203-2-2019
STANDARD 7203-2
Third edition
2019-07
Reference number
ISO 7203-2:2019(E)
© ISO 2019
ISO 7203-2:2019(E)
Contents Page
Foreword .......................................................................................................................................................................................................................................... v
Introduction ................................................................................................................................................................................................................................ vi
1 Scope ................................................................................................................................................................................................................................. 1
2 Normative re ferences ...................................................................................................................................................................................... 1
3 Terms and definitions ..................................................................................................................................................................................... 1
4 Classification and uses o f foam concentrates ......................................................................................................................... 4
4. 1 ............................................................................................................................................................................................. 4
C las s ificatio n
Annex A (normative) Preliminary sampling and conditioning o f the foam concentrate ............................... 8
Annex B (normative) Determination o f tolerance to freezing and thawing ................................................................ 9
Annex C (normative) Determination o f volume percentage o f sediment ................................................................... 11
Annex D (normative) Determination o f viscosity for pseudo-plastic foam concentrates .......................... 12
Annex E (normative)
Determination o f surface tension, interfacial tension and spreading
coe fficient ................................................................................................................................................................................................................. 14
Annex F (normative) Determination o f expansion and drainage time for medium-
expansion foam concentrates .............................................................................................................................................................. 15
Annex G (normative) Determination o f expansion anddrainage time for high-expansion
foam concentrates ............................................................................................................................................................................................ 20
Annex H (normative)
Determination o f test fire performance formedium-expansion foam
concentrates ........................................................................................................................................................................................................... 26
Annex I (normative)
Determination o f test fire performance forhigh-expansion foam
concentrates ........................................................................................................................................................................................................... 31
Annex J(informative) Determination of radiation measurement method................................................................ 36
Annex K (informative) Compatibility ................................................................................................................................................................ 40
Bibliography ............................................................................................................................................................................................................................. 41
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work o f preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters o f
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the di fferent approval criteria needed for the
di fferent types o f ISO documents should be noted. This document was dra fted in accordance with the
editorial rules o f the ISO/IEC Directives, Part 2 (see www.iso .org/directives).
Attention is drawn to the possibility that some o f the elements o f this document may be the subject o f
patent rights. ISO shall not be held responsible for identi fying any or all such patent rights. Details o f
any patent rights identified during the development o f the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www.iso .org/patents).
Any trade name used in this document is in formation given for the convenience o f users and does not
constitute an endorsement.
For an explanation o f the voluntary nature o f standards, the meaning o f ISO specific terms and
expressions related to con formity assessment, as well as in formation about ISO's adherence to
the World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see
www.iso .org/iso/foreword .html.
This document was prepared by Technical Committee ISO/TC 21, Equipment for fire protection and fire
.
fighting , Subcommittee SC 6, Foam and powder media and firefighting systems using foam and powder
This third edition cancels and replaces the second edition (ISO 7203-2:2011), which has been technically
revised.
The main changes compared to the previous edition are:
— addition o f Clause 4 containing specifications for Class A foam concentrates;
— extension o f Clause 2 ;
— modification o f Clause 12 to run two tests instead of one and take the average of both values instead
having just one datum;
— correction o f several figures;
— the extension o f Annex H by a scheme o f a decision tree and the modification o f the acceptable
temperature range for testing fire per formance;
— removal o f Annex “Typical anticipated per formance for various types o f foam concentrate”.
A list of all parts in the ISO 7203 series can be found on the ISO website.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www.iso .org/members .html.
Introduction
Firefighting foams are widely used to control and extinguish fires o f Class B (flammable liquids) and/or
Class A fuels (solid materials, usually o f an organic nature) and for inhibiting reignition.
Foams can be used in combination with other extinguishing media, in particular halons, carbon dioxide
and powders, which are the subject o f other International Standards, including, ISO 6183, ISO 7201-1,
ISO 7201-2 and ISO 7202. A specification for foam systems can be found in ISO 7076.
Attention is drawn to Annex K, which deals with the compatibility of foam concentrates, and the
compatibility o f foams and powders.
1 Scope
T h i s do c u ment s p e ci fie s the e s s enti a l prop er tie s and p er forma nce o f l iquid fo am concentrate s u s e d
to ma ke me d iu m- or h igh- exp a n s ion fo a m s or b o th for the control, the e xti nc tion and the i n h ibition o f
comply with I S O 7 2 03 -1 are a l s o s uitable for top appl ic ation to fi re s o f water-i m m i s c ible l iquid s .
2 Normative re ferences
T he fol lowi ng do c uments a re re ferre d to i n the te xt i n s uch a way that s ome or a l l o f thei r content
con s titute s re qui rements o f th i s do c u ment. For date d re ference s , on ly the e d ition c ite d appl ie s . For
u ndate d re ference s , the late s t e d ition o f the re ference d do c u ment (i nclud i ng any amend ments) appl ie s .
I S O 3 0 4, Surface active agents — Determination o f surface tension by drawing up liquid films
I S O 3 10 4, Petroleum products — Transparent and opaque liquids — Determination o f kinematic viscosity
ISO and IEC maintain terminological databases for use in standardization at the following addresses:
— f https: //www.iso .org/obp
I S O O n l i ne brows i ng plat orm: avai lable at
3.1
characteristic value
va lue de clare d by the fo am concentrate s uppl ier for the chem ic a l a nd phys ic a l prop er tie s and the
3.2
25 % drainage time
ti me for 2 5 % o f the l iqu id content o f a fo am to d rai n out
3.3
expansion
ratio of the volume of foam to the volume of the foam solution from which it was made
3.4
low-expansion
expansion (3.3
) in the range 1 to 2 0 , a s appl ie d to fo a m and to a s s o c iate d e quipment, s ys tem s a nd
concentrates
3.5
medium-expansion
expansion (3.3
) i n the ra nge 2 1 to 2 0 0 , a s appl ie d to fo am and to as s o c iate d e qu ipment, s ys tem s a nd
concentrates
3.6
high-expansion
expansion (3.3
) gre ater tha n 200, as appl ie d to fo am and to as s o c iate d e qu ipment, s ys tem s a nd
concentrates
3.7
foam
< fi refighti ng> aggre gate o f a i r-fi l le d bub ble s forme d from an aque ou s s olution o f a s u itable fo am
concentrate
3.8
concentrate
< fo am> l iqu id th at, when m i xe d with water i n the appropri ate concentration, give s a fo am s olution
3.9
protein foam concentrate
P
foam concentrate (3.8 ) derive d from hyd rolys e d pro tei n materia l s
3.10
fluoroprotein foam concentrate
FP
protein foam concentrate (3.8 ) with adde d fluori nate d s ur face -ac tive agents
3.11
synthetic foam concentrate
S
foam concentrate (3.8 ) b as e d on a m i x tu re o f hyd ro c arb on s ur face -ac tive agents and wh ich c an conta i n
3.12
alcohol-resistant foam concentrate
AR
foam concentrate (3.8) resistant to breakdown when applied to the surface of alcohol or other water-
miscible solvents
3.13
aqueous film- forming foam concentrate
AFFF
foam concentrate (3.8) based on a mixture of hydrocarbon and fluorinated surface-active agents with
the ability to form an aqueous film on the sur face o f some hydrocarbons
3.14
film- forming fluoroprotein foam concentrate
FFFP
fluoroprotein foam concentrate (3.8 ) that has the ability to form an aqueous film on the sur face o f some
hydrocarbons
3.15
foam solution
solution of foam concentrate (3.8) and water
3.16
force ful application
application o f foam such that it falls directly onto the sur face o f a liquid fuel
3.17
gentle application
application o f foam indirectly to the sur face o f a liquid fuel via a backboard, tank wall or other sur face
3.18
sediment
insoluble particles in the foam concentrate
3.19
spreading coe fficient
value calculated from the measured sur face and inter facial tensions to indicate the ability o f one liquid
to spontaneously spread across the sur face o f another
3.20
temperature for use
maximum and minimum temperatures claimed by the manu facturer between which the foam
concentrate is ready for use
3.21
fluorine free foam concentrate
F3
foam concentrate (3.8) which does not form an aqueous film on hydrocarbon fuels, but which is
targeting Class B per formance at force ful application and which does not contain any fluorochemicals
3.22
Class A foam concentrate
foam concentrate (3.8
) for use on Class A fires
3.23
Class A fire
fire involving solid materials, usually o f an organic nature, in which combustion normally takes place
with the formation of glowing embers
Note 1 to entry: Adapted from ISO 3941:2007, Clause 2.
Note 2 to entry: Class A fires involve solid materials, usually o f an organic nature (such as vegetation, wood, cloth
and paper), rubber, and some plastics, in which combustion can occur at or below the sur face o f the material with
or without the formation of glowing embers.
4.1 Classification
The foam concentrate shall be classified as medium- or high- expansion or both and shall comply with
the appropriate requirements.
8.1 pH limits
T he pH o f the fo a m concentrate, b e fore and a fter temp eratu re cond itioni ng i n accorda nce with A.2 ,
conditioning in accordance with A.2 , at the s uppl ier's re com mende d concentration, sha l l b e with i n
±10 % o f the charac teri s tic va lue when de term i ne d i n accorda nce with E.2.
9.2 Temperature sensitivity
T he s ur face ten s ion o f the fo am s olution prep a re d from the concentrate, a fter temp eratu re cond ition i ng
in accordance with A.2 , at the s uppl ier's re com mende d concentration, s ha l l b e de term i ne d i n accordance
with E.2.
T he va lue ob tai ne d a fter temp eratu re cond ition i ng s ha l l no t b e le s s than 0 ,9 5 ti me s , or more tha n
10.1 General
I nter fac ia l ten s ion sh a l l on ly b e te s te d on fo am agents wh ich a re de clare d b y the manu fac tu rer to b e
ten s ion f
b e twe en the o am f
s olution f
prep a re d rom the o am concentrate and c yclohexa ne (when
determined in accordance with E.3) and (b) the characteristic value for interfacial tension shall not
e xce e d 1 , 0 m N/m or 10 % o f the ch arac teri s tic va lue, wh ichever i s gre ater.
0 , 5 m N/m .
Before and after temperature conditioning in accordance with A.2 , the spreading coefficient of the foam
solution prepared from a concentrate claimed by the supplier to be “film- forming” shall be positive
when calculated in accordance with E.4.
NOTE Foam concentrates con forming with this clause are more likely to be o f type AFFF or FFFP than o f
type FP, P, F3 or S.
12 Expansion
14.1 Marking
i) b atch nu mb er;
j) word s “No t s uitable for u s e with s e a water ” or “Su itable for u s e with s e a water ”, a s appropri ate .
WARNING — It is extremely important that the foam concentrate, a fter dilution with water to
the recommended concentration, shall not, in normal usage, present a significant toxic hazard
to li fe in relation to the environment.
NO TE Re co m mende d s torage temp eratu re a nd temp eratu re o f u s e a re the s a me i f the p ro duc t i s m a rke d “do
no t fre e z e”.
14.1.4 Fo am co ncentrates co mp lying with I S O 7 2 0 3 - 1 s hall als o b e marked “lo w- exp ans io n”.
14.1.5 Fo am co ncentrates in acco rdance with I S O 7 2 0 3 - 3 s hall als o b e marked “alco ho l res is tant”.
14.2 Packaging
The packaging of the foam concentrate shall ensure that the essential characteristics of the concentrate
a re pre s er ve d when s tore d and ha nd le d i n accorda nce with the s uppl ier's re com mendation s .
14.3.1 I f reques ted by the us er, the s up p lier s hall p rovide a lis t o f the characteris tic values .
14.3.2 I f the fo am co ncentrate is N ewto nian and the vis co s ity at the lo wes t temp erature fo r us e is mo re
than 200 mm2 /s when meas ured in acco rdance with I S O 3 1 0 4, it s hall b e marked with the wo rds “This
14.3.3 I f the fo am co ncentrate is p s eudo - p las tic and the vis co s ity at the lowes t temp erature fo r us e is
greater than o r equal to 1 2 0 mPa⋅ s at 3 7 5 /s , it s hall b e marked “This co ncentrate can require s p ecial
Annex A
(normative)
Preliminary sampling and conditioning o f the foam concentrate
A.2.1 I f the s up p lier claims that the co ncentrate is no t advers ely a ffected by freezing and thawing,
co nditio n the co ncentrate s amp le thro ugh fo ur cycles o f freezing and thawing, generally as des crib ed
in B.2 , b e fo re co nditio ning in acco rdance with A.2.2 . I f the fo am co ncentrate is advers ely a ffected by
freezing and thawing, it s hall b e co nditio ned acco rding to A.2.2 without prior freezing and thawing.
A.2.2 C o nditio n the co ncentrate in the s ealed co ntainer fo r 7 d at (6 0 ± 2 ) °C , fo llo wed by 1 d at
(2 0 ± 5 ) °C .
Annex B
(normative)
Determination o f tolerance to freezing and thawing
B.1 Apparatus
The usual laboratory apparatus and, in particular, the following.
B.1.1 Freezing chamber, capable o f achieving the temperatures required in B.2.
B.1.2 Polyethylene tube , approximately 10 mm in diameter, approximately 400 mm long and sealed
and weighted at one end, with suitable spacers attached.
Figure B.1 shows a typical form.
B.1.3 Measuring cylinder, glass, o f 500 ml capacity, approximately 400 mm high and approximately
65 mm in diameter, with a stopper.
B.2 Procedure
Set the temperature of the freezing chamber (B.1.1) to at least 10 °C below the freezing point of the
sample, measured in accordance with BS 5117-1.3, excluding 5.2.
To prevent the glass measuring cylinder ( B.1.3 ) from breaking due to expansion o f the foam concentrate
on freezing, insert the tube ( B.1.2 ) into the measuring cylinder with the sealed end downward, weighted
i f necessary to avoid flotation, the spacers ensuring it remains approximately on the central axis o f the
cylinder. Fill the cylinder and fit the stopper.
Place the cylinder in the freezing chamber, cool it and maintain at the required temperature for 24 h.
At the end o f this period, thaw the sample for not less than 24 h and not more than 96 h in an ambient
temperature o f (20 ± 5) °C.
Repeat three times to give four cycles o f freezing and thawing be fore testing.
Examine the sample for stratification and non-homogeneity.
Key
1 spacers (e.g. plastic cable strap)
2 mass at sealed end
Figure B.1 — Typical form o f polyethylene tube
Annex C
(normative)
Determination o f volume percentage o f sediment
C.1 Sampling
Use a sample prepared in accordance with A.1 . Ensure that any sediment is dispersed by shaking the
sample container. Take two samples, testing one immediately and the other a fter ageing for (24 ± 2) h at
(60 ± 2) °C in a filled container without access to air.
C.2 Apparatus
C.2 .3 Sieve , o f nominal aperture size 180 µm, complying with ISO 3310-1.
C.3 Procedure
Centri fuge each sample o f the concentrate for (10 ± 1) min. Determine the volume o f the sediment and
record it as a percentage of volume of the centrifuged sample volume.
Wash the contents of the centrifuge tube (C.2.1) onto the sieve (C.2.3) and check whether the sediment
can or cannot be dispersed through the sieve by the jet from the plastic wash bottle (C.2.4).
Annex D
(normative)
Determination o f viscosity for pseudo-plastic foam concentrates
D.1 General
This annex gives the procedure for determining the viscosity for pseudo-plastic foam concentrates. The
procedure is described in ISO 3219.
NOTE Pseudo-plastic foam concentrates are a particular class of non-Newtonian foam concentrate and have
a viscosity which decreases with increasing shear rate at constant temperature.
D.2.1 Apparatus
The usual laboratory apparatus and the following.
D.2.1.1 Rotational viscometer, in accordance with ISO 3219 with the following parameters:
— maximum shear stress o f ≥75 Pa;
— maximum shear rate o f ≥600/s.
The viscometer shall be fitted with a temperature control unit which can maintain the sample
temperature within ±1 °C o f the required temperature.
D.2.2 Test temperatures
The viscosity o f the foam concentrate shall be measured from 20 °C down to, and including, the lowest
temperature for use claimed by the manu facturer, in increments o f 10 °C. Use a fresh sample for each
temperature.
D.2.3 Viscosity measurement
I f the sample contains suspended air bubbles, the sample shall be centri fuged for 10 min using the
apparatus specified in C.2.1 and C.2.2 before the sample is placed in the apparatus.
The test should be performed according to the following test procedure:
a) Adjust the temperature control unit.
b) Set the gap.
c) Apply the sample.
d) Wait a minimum o f 10 min (with no shear) to reach temperature equilibrium.
e) Pre-shear for 1 min at 600/s.
f) Wait 1 min without shearing.
g) Measure the shear stress for 10 s at each shear rate, starting at the lowest shear rate (pre ferably
at 75/s).
12 © ISO 2019 – All rights reserved
ISO 7203-2:2019(E)
h) M e a s ure the s he ar s tre s s at a m i n i mu m o f eight d i fferent s he ar rate s over the range (0/s to 6 0 0/s) ,
e . g. 75/s , 1 5 0/s , 2 2 5/s , 3 0 0/s , 3 75/s , 45 0/s , 5 2 5/s , 6 0 0/s . C a lc u l ate the app a rent vi s co s ity, v,
expre s s e d i n m i l l ip a s c a l- s e cond s , a s given i n Formula (D.1)
s
v = 1 000 × 1
s2
(D.1)
where
s1 i s the she a r s tre s s , expre s s e d i n p a s c a l s;
D.2.4 Results
Rep or t the re s u lts a s a table i nclud i ng te s t temp eratu re, e xpre s s e d i n degre e s C el s iu s , the she ar rate,
e xpre s s e d i n re c ipro c a l s e cond s , the s he ar s tre s s , expre s s e d i n re cipro c a l s e cond s , and the app arent
Annex E
(normative)
Determination o f surface tension, interfacial tension and
spreading coe fficient
E.1.1 Solution o f foam concentrate , at the reco mmended co ncentratio n fo r us e in fres hly made
analytical water co mp lying with grade 3 of I SO 3 696: 1 9 87 and with s ur face tens io n no t les s than
70 mN/m.
NO TE T he s olution c a n b e m ade up i n a 10 0 m l vo lu me tr ic fl a s k, u s i ng a pip e tte to me a s u re the fo a m
concentrate.
E.1.2 Cyclohexane , o f p urity no t les s than 9 9 %, fo r inter facial tens io n and s p reading co e fficient o nly.
Yf i s the s u r face ten s ion o f the fo a m s olution, e xpre s s e d i n m i l l i new ton s p er me tre;
Yi i s the i nter fac ia l ten s ion b e twe en the fo am s olution and c yclohe xa ne, expre s s e d i n m i l l i new ton s
per metre.
Annex F
(normative)
Determination o f expansion and drainage time for medium-
expansion foam concentrates
F.1 Apparatus
The usual laboratory apparatus and, in particular, the following.
F.1.1 Collecting vessel , plastic, cylindrical, o f volume known to ±1 %, equipped with a bottom
discharge facility, as shown in Figure F.1.
F.1.2 Foam-making equipment, with nozzle as shown in Figures F.2 and F.3 which, when tested
with water, has a flow rate o f between 3,1 l/min and 3,4 l/min at a nozzle pressure o f (500 ± 10) kPa
[(5,0 ± 0,1) bar].
F.3 Procedure
F.3.1 Prepare two samples of foam concentrate in accordance with Annex A. Condition one in
accordance with Annex A.
F.3.2 Carry out the remainder o f the procedure for each sample on the same day. Prepare a foam
solution o f each sample following the supplier's recommendations for concentration, maximum premix
time, compatibility with the test equipment, avoiding contamination by other types o f foam, etc. Use
potable water to make up the foam solutions and, i f the supplier claims that the concentrate is suitable for
sea water, also make foam solutions at the same concentration using the synthetic sea water prepared in
accordance with F.4. The concentration used in synthetic sea water shall be the same as the concentration
used in potable water.
F.3.3 Wet the vessel internally and weigh it. Record the mass as m 1 . Set up the foam equipment and
adjust the nozzle pressure to within the range (500 ± 10) kPa [(5,0 ± 0,1) bar] to give a flow rate between
3,1 l/min and 3,4 l/min. With discharge facility closed, collect foam, taking care that voids are not formed
in the vessel, and start the timing device when the vessel is half full. As soon as the vessel is full, stop
collecting foam and strike the foam surface level with the rim, and clean the exterior surface o f the vessel
of foam. Weigh the vessel and record the mass as m 2 .
Calculate the expansion, E, from Formula (F.1):
V
E=
m2 − m1
(F.1)
where
V is the vessel volume, expressed in litres;
m1 is the mass, expressed in kilograms, o f the empty vessel;
m2 is the mass, expressed in kilograms, o f the full vessel.
Assume that the density o f the foam solution is 1,0 kg/l.
Open the drainage facility and measure the 25 % and 50 % drainage time. Determine the drainage
either by placing the vessel on a set o f scales and recording the mass loss or by collecting the drained
foam solution in a measuring cylinder. Adjust the drainage facility such that the drained foam solution
can flow out but the passage o f foam is prevented. For each sample carry out the test three times.
F.3.4 For each sample, calculate the mean values o f the three tests for the expansion and 25 % and
50 % drainage time.
F.4 Synthetic sea water
Prepare the synthetic sea water by dissolving the components as given in Table F.1.
Table F.1 — Components o f synthetic sea water
Dimensions in millimetres
Key
1 f
b o tto m dis charge acility
Dimensions in millimetres
Key
1 ring Number Size
2 net 1
3 pipe 1
4 nut 1
5 acorn nut 1 M6M 6
6 nipple 3 MHM 6
7 tee 1 G- 1 /4″- 1 /8 ″
8 nipple 1 G- 1 /4″
9 valve 1 G- 1 /4″
10 nipple 1 G- 1 /4″
11 nozzle 1 G- 1 /4″- 3 /8 ″
12 collar 1 G- 1 /8 ″ GG3 , 5
13 pressure gauge 1 12
1 G- 1 /4″ 1 - 1 , 6 M Pa D = 40
a The no zzle s hall b e co axial with the b arrel o f the fo am b ranch.
b The pressure gauge shall be positioned so as not to interfere with the air inlet of the branch.
Figure F.2 — Medium-expansion foam-making nozzle
Dimensions in millimetres
Key
a The s creen s hall b e 2 4 mes h p er inch, with a wire diameter o f 0 , 4 mm.
Annex G
(normative)
Determination o f expansion and drainage time for high-expansion
foam concentrates
G.1 Apparatus
The usual laboratory apparatus and, in particular, the following.
G.1.1 Collecting vessel (see Figure G.1), o f volume, V, o f approximately 500 l and that is accurately
known to ±5 l, equipped with a drain at the base.
G.1.2 High-expansion foam generator, with nozzle as shown in Figures G.2, G.3 and G.4 that, when
tested with water, has a flow rate o f between 6,0 l/min and 6,2 l/min at a nozzle pressure o f (500 ± 10) kPa
[(5,0 ± 0,1) bar].
G.3 Procedure
G.3.1 Prepare two samples of foam concentrate in accordance with Annex A. Condition one in
accordance with Annex A.
G.3 .2 Carry out the remainder o f the procedure for each sample on the same day. Prepare a foam
solution o f each sample following the supplier's recommendations for concentration, maximum
premix time, compatibility with the test equipment, avoiding contamination by other types o f foam,
etc. Use potable water to make up the foam solutions and, i f the supplier claims that the concentrate is
suitable for sea water, also make foam solutions at the same concentration using the synthetic sea water
prepared in accordance with G.4. The concentration used in synthetic sea water shall be the same as the
concentration used in potable water.
G.3 .3 Wet the vessel internally and weigh it. Record the mass as m 1 . Set up the foam equipment and
adjust the nozzle pressure within the range (500 ± 10) kPa [(5,0 ± 0,1) bar] to give a flow rate o f between
6,0 l/min and 6,2 l/min. With the drain at the base closed, collect foam, taking care that voids are not
formed in the vessel. Start the timing device when the vessel is hal f full. As soon as the vessel is full, stop
collecting foam, strike the foam surface level with the rim, and clean the exterior surface o f the vessel o f
foam. Weigh the vessel and record the mass as m 2 .
Calculate the expansion, E, from Formula (G.1) :
V
E= (G.1)
m 2 − m1
where
V is the vessel volume, expressed in litres;
m1 is the mass, expressed in kilograms, of the empty vessel;
m 2 is the mass, expressed in kilograms, of the full vessel.
Assume that the density o f the foam solution is 1,0 kg/l.
Open the drainage facility and measure the 25 % and 50 % drainage time. Determine the drainage
either by placing the vessel on a set o f scales and recording the mass loss or by collecting the drained
foam solution in a measuring cylinder. Adjust the drainage facility such that the drained foam solution
can flow out but the passage o f foam is prevented. For each sample, carry out the test three times.
G.3.4 For each sample, calculate the mean values o f the three tests for the expansion and the 25 % and
50 % drainage time.
G.4 Synthetic sea water
Prepare the synthetic sea water by dissolving the components as given in Table G.1 .
Table G.1 — Components o f synthetic sea water
Dimensions in millimetres
Key
1 f
b o tto m dis charge acility
Dimensions in millimetres
Key
1 housing Number Dimension Material
2 ring 1
3 perforated plate 1
4 motor (1 400 rpm; 0,3 HP; 50 Hz; 3 ph; 380 VAC) 1 1 mm SS 1312
5 fan (1 400 rpm; 7,5 mm water, 2 000 m 3 /h) ∅405 mm, ∅10 × 12
6 screw 1
7 nut 1
8 washer 8 M6S 6 × 16 SS 2343
9 support 8 M6M 6 SS 2343
10 screw 8 RB 6,4 SS 2343
11 washer 2
12 nut 20 M6S 6 × 14 SS 2343
13 nut 20 RB 8,4 SS 2343
14 screen 6 M6M 8 SS 2343
15 valve 4 MVM-K 6 SS 2343
16 pressure gauge 1
17 tee 1 OLO R ¼″
18 nipple 1 ∅63R¼″,0-10 bar galvanized
19 pipe 1 galvanized
20 bend 2
21 nozzle 1
22 inspection cover 1 galvanized
23 screw 1 ¼″HH 6,5
24 washer 1
25 handle 1 M6S 5 × 16 SS 2343
1 ∅18/5,5 × 2 SS 2343
Figure G.2 — High-expansion foam generator — General arrangement
Dimensions in millimetres
Key
1 housing (2 mm plate)
2 ring
26 collar
27 and 28 screen supports (2 mm plate)
29 bar reinforcement
30 legs
31 screw
32 nut
Figure G.3 — High-expansion foam generator — Housing (1)
Dimensions in millimetres
Key
33 s up p o rt ring (1 , 5 mm p late)
Annex H
(normative)
Determination o f test fire performance for medium-expansion
foam concentrates
H.1 General
T h i s an nex s p e ci fie s the pro ce du re for de term i n i ng the tes t fi re p er formance for me d iu m- e xp an s ion
fo a m concentrate s . T he te s ts de s c rib e d i n th i s a n nex are more e xp en s ive and ti me - con s u m i ng tha n the
o ther te s ts des c rib e d i n th i s do c u ment. I t i s re com mende d that they b e ca rrie d out at the end o f the te s t
neither are successful). The concentrate conforms to Clause 13 if two tests are successful.
H.2.1.2 Foam concentrates compatible with sea water
C onduc t one te s t with p o table water (tes t 1) and the o ther (te s t 2 ) with s ynthe tic s e a water o f the
composition given in F.4 . I f b o th a re s ucce s s fu l, rep e at the te s t with the gre ater o f the two ex ti nc tion
ti mes (te s t 3 ) . I f the e xti nc tion ti me s a re identic a l, rep e at the s e a water te s t. I f the rep e at te s t i s
I f the rep e at te s t i s u n s ucce s s fu l, ca rr y out a fu r ther rep e at te s t (te s t 4) . I f that te s t then fa i l s , term i nate
that series.
I f one o f the fi rs t two te s ts (te s t 1 or 2 ) i s no t s ucce s s fu l , rep e at that te s t. I f th i s rep e at te s t i s s ucce s s fu l,
conduc t a s e cond rep e at te s t; o ther wi s e term i nate the te s t s erie s . T he concentrate con form s to
Figure H.1 — Decision tree for fire per formance test on water-immiscible fuels
— ai r temp erature (5 − 4 0) ° C;
H.2 .4 Records
a) lo c ation;
b) ai r temp erature;
c) fuel temperature;
d) water temperature;
e) foam solution temperature;
f ) wind speed;
g) 90 % control time;
h) 99 % control time;
i) extinction time;
j) 1 % burn-back time.
It is recommended that the time is recorded at 1 % burn-back. Control times and burn-back time can be
determined either visually by an experienced person or from thermal radiation measurements. Annex J
gives details o f a method suitable for medium-expansion foams.
H.2.5 Foam solution
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 o f foam, etc.
Use potable water to prepare the foam solution and, i f the supplier claims that the concentrate is
suitable for use in sea water, make a second foam solution at the same concentration using synthetic sea
water in accordance with G.4.
H.2.6 Fuel
Use an aliphatic hydrocarbon mixture having physical properties according to the following
specification:
a) distillation range: 84 °C to 105 °C;
b) maximum di fference between initial and final boiling points: 10 °C;
c) maximum aromatic content: 1 % mass fraction;
d) density at 15 °C: (700 ± 20) kg/m 3 .
NOTE 1 The normal value o f sur face tension o f the aliphatic hydrocarbon mixture measured in accordance
with H.2.1 is 21 mN/m to 22 mN/m.
NOTE 2 Typical fuels meeting this specification are certain solvent fractions sometimes re ferred to as
commercial heptane.
H.3.1.1 Circular fire tray, stainless steel grade X5CrNi18-10 (ISO 3506: A2; ASTM: 304304; UNS:
S30400), with dimensions as follows:
— internal diameter at rim (1 480 ± 15) mm;
— depth (150 ± 10) mm;
— nominal thickness o f steel wall 2,5 mm
NOTE The tray has an area o f approximately 1,73 m 2 .
Place the tray directly on the ground and ensure that it is level. Add approximately 30 l o f water and
(55 ± 2) l o f fuel to give a nominal 50 mm fuel depth, with approximately 100 mm between the fuel
sur face and the upper rim o f the tray wall.
Suspend the burn-back pot containing (0,9 ± 0,1) l o f fuel on the sheltered side o f the fire tray.
Ignite the fuel not less than 3 min and not more than 5 min after adding it. Not less than 45 s after full
involvement o f the sur face o f the fuel, mount the medium-expansion nozzle horizontally on the rim o f
the tray, as shown in Figure H.2 . Start foam application (60 ± 2) s a fter full involvement. Apply foam for
(120 ± 2) s. Record the extinction time as the time a fter the start o f foam application at which all flames
in the fire tray are extinguished. Following foam application, allow the fire in the burn-back pot to burn
until sustained flames appear above the foam blanket. Record this time as the 1 % burn-back time.
I f the burn-back pot is extinguished due to overflow o f foam during foam application, re-ignite it
immediately.
Key
1 foam-making nozzle
2 tray
3 burn-back pot, suspended outside tray
4 fuel
5 water
Figure H.2 — Test fire arrangement for medium-expansion foam
Annex I
(normative)
Determination o f test fire performance for high-expansion foam
concentrates
I.1 General
T h i s an nex s p e c i fie s the pro ce dure for de term i n i ng the te s t fi re p er formance for h igh- exp an s ion fo am
concentrate s . T he te s ts de s c rib e d i n th i s an ne x a re more exp en s ive and ti me - con s um i ng tha n the o ther
te s ts de s crib e d i n th i s do c u ment. I t i s re com mende d th at they b e c a rrie d out at the end o f the te s t
neither are successful). The concentrate conforms to Clause 13 if two tests are successful.
I.2.1.2 Foam concentrates compatible with sea water
C onduc t one te s t with p o table water (te s t 1) a nd the o ther (te s t 2 ) with s ynthe tic s e a water o f the
composition given in G .4. I f b o th a re s ucce s s fu l , rep e at the te s t with the gre ater o f the two e xti nc tion
ti me s (te s t 3 ) . I f the e xti nc tion ti me s a re identic a l , rep e at the s e a water te s t. I f the rep e at te s t i s
I f the rep e at te s t i s un s ucce s s fu l , c arr y out a fur ther rep e at te s t (te s t 4) . I f that te s t then fa i l s , term i nate
that series.
I f one o f the fi rs t two te s ts (te s t 1 or 2 ) i s no t s ucce s s fu l, rep e at th at te s t. I f th i s rep e at te s t i s s ucce s s fu l,
conduc t a s e cond rep e at te s t; o ther wi s e term i nate the te s t s erie s . T he concentrate con form s to
Figure I.1 — Decision tree for fire per formance test on water-immiscible fuels
— ai r temp eratu re (5 − 4 0) ° C;
— ma xi mu m wi nd s p e e d i n the 3 m/s.
proxi m ity o f the fi re tray
NO TE I f ne ce s s a r y, s o me fo rm o f wi nd- s c re en c a n b e u s e d .
I.2 .4 Records
a) lo c ation;
c) f uel temperature;
d) water temperature;
e) f oam solution temperature;
f ) wind speed;
g) 90 % control time;
h) 99 % control time;
i) extinction time.
NOTE Control times can be determined visually by an experienced person.
I.3.1.1 Circular fire tray, stainless steel grade X5CrNi18-10 (ISO 3506: A2; ASTM: 304304; UNS:
S30400), with dimensions as follows:
— internal diameter at rim (1 480 ± 15) mm;
— depth (150 ± 10) mm;
— nominal thickness o f steel wall 2,5 mm.
NOTE The tray has an area o f approximately 1,73m 2 .
I.3.1.2 High-expansion foam generator, as described in G.1.2, mounted horizontally (650 ± 50) mm
above the ground.
I.3.1.3 Fire screens , o f nominal 5 mm square metal mesh, to form the nominal arrangement shown in
Figure I.2.
I.3.2 Test procedure
Place the tray directly on the ground and ensure that it is level. Add approximately 30 l o f water and
(55 ± 2) l o f fuel to give a nominal 50 mm fuel depth, with approximately 100 mm between the fuel
sur face and the upper rim o f the tray wall.
Place the net screens around the fire tray as shown in Figure I.2. Ignite the fuel not less than 3 min and
not more than 5 min a fter adding it. Not less than 45 s a fter full involvement o f the sur face o f the fuel,
commence foam generation with the foam generator no nearer than 3 m to the tray.
Wait (60 ± 2) s a fter full involvement, then move the foam generator to the opening in the net screen
and apply foam to the fire. Apply foam for (120 ± 2) s. Record the extinction time as the period from the
start o f foam application to extinction.
Dimensions in metres
Key
1 foam-making nozzle
2 tray
3 burn-back pot, suspended outside tray
4 fuel
5 water
NOTE All dimensions are nominal.
Figure I.2 — Test fire arrangement for high-expansion foam
Annex J
(informative)
Determination o f radiation measurement method
J.1 Evaluation
Rad i ation me as u rement i s a conven ient a nd obj e c tive way to monitor the p er formance o f a fo am du ri ng
the fi re p er formance te s t. I t re duce s the ne e d for vi s ua l ob s er vation s (excep t for fl ame fl ickers and ti me
T h i s an nex de s crib e s the e qu ipment and pro ce du re u s e d i n a s erie s o f te s ts i n one te s ti ng lab orator y,
and the methods used to interpret and present the results. See Reference [6 ] for de ta i l s . T he me tho d i s
s u itable for low- and me d iu m- exp an s ion fo am s , but no t for h igh- exp a n s ion fo am s .
Rad i ation level s s hou ld b e re corde d conti nuou sly or with i nter va l s no t exce e d i ng 1 s .
Dimensions in metres
Key
1 radiometer
2 circular fire tray
Figure J.1 — Location o f radiometers for recording heat radiation during fire per formance tests
J.4 Procedure
Correct the output from the two radiometers by deducting the background radiation recorded from 5 s
to 10 s a fter the moment o f complete extinction.
Determine the average value of the two radiometers.
Determine the average value of time of recorded radiation during the 25 s period beginning at 30 s
before the start of the foam application and ending 5 s before the start of foam application (see
Figure J.2 ).
Determine the relative radiation by dividing the output by the average value obtained in accordance
with the preceding paragraph.
The instantaneous radiation values are subject to random fluctuation. A smoother curve, which
facilitates interpretation, can be obtained by plotting radiation values averaged over a period o f ±5 s for
each time value.
The adjusted relative radiation is shown for the extinguishing test in Figure J.3 and for the burn-back
test in Figure J.4. A control of 90 % is equivalent to the relative radiation 0,1.
The description above implies that computer-controlled measuring practices should be applied.
1) The Medtherm Series 64 supplied by Medtherm Corp., PO Box 412, Huntsville, AL, USA is an example o f a
suitable product (apparatus) available commercially. This in formation is given for the convenience o f users o f this
document and does not constitute an endorsement by ISO o f this product (apparatus).
© ISO 2019 – All rights reserved 37
ISO 7203-2:2019(E)
Key
X time, exp res s ed in minutes
NOTE Foam application starts at 1 min and stops at 5 min. The burn-back test starts at 15 min.
Figure J.2 — Typical absolute radiation levels throughout a test
Key
X time, exp res s ed in minutes
NOTE Foam application starts at 0 min and stops at 4 min. 90 % control is achieved at about 1 min 8 s.
Figure J.3 — Typical relative radiation levels during extinction
Key
X time, exp res s ed in minutes
Annex K
(informative)
Compatibility
Bibliography
safe handling and transfer procedures o f halon 1211 and halon 1301
[6 ] I S O 7 2 02 , Fire protection — Fire extinguishing media — Powder
[7 ] NORD T E S T Me tho d N T Fi re 02 3 , Fi re E x ti ngui s h i ng Fo am C oncentrate s
ICS 13.220.10
Price based on 41 pages
© ISO 2019 – All rights reserved