BRITISH STANDARD AEROSPACE SERIES BS EN 2155 12 1997 Test methods for transparent materials for aircraft glazing — Part 12 Determination of linear thermal expansion The European Standard EN 2155 12 19[.]
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Sum mary of pag es
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theEN title p g e, p g es 2 to 5 and a b ck cov er
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Trang 3Pag e
Trang 5NORME EUROPÉENNE
July 19 7
ICS 4 0 5.4
Des riptor : Air raft in ustry, g lazing , materials,transp rency,plastic ,tests,determination, thermal pro erties, thermal e p nsion
Eng lish ver ion
Série aérosp tiale — Méthodes d’es ais pour
matériaux transparents pour vitrag es
aéronautiques — Partie 1 : Détermination de
la diatation thermique lnéaire
Luft- und Raumfahrt — Prüfver ahren für
transp rente W erkstofe zur Verg lasung von
Luftfahr eug en — Tei 1 : Bestimmung der
l nearen W ärmeausdehnung
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Ref No EN 2 5 -1 :19 7 E
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Contents
Pag e
Fig ure 1 — Quartz-tube diatometer 5
Trang 71 Scope
This stand rd specifies the method to determine the
rev er ible lnear thermal ex ansion of plastic with
exclusion of chang es in leng th due to ac idental
factor such as chang es in moisture content, deg re
of poly merization and stres release Since it wi
not be pos ible to exclude al these ac idental
factor , the method can be ex ected to g iv e only
a proximate v alues
2 Definition
For the purposes of this stand rd, the folowing
definition a pl es:
Linear thermal ex ansion is defined as the chang e
in leng th of a material in relation to u it leng th for
a v ariation in temperature of 1 °C
3.1 Dil a tometer
A simple fused-quartz tube diatometer is shown in
Fig ure 1 Any g eneraly ac epted method of
measuring thermal ex ansion ma be used which
wi l be ac urate to within ± 10% The ac uracy of
the dev ice which measures the ex ansion shal be
such that it measures the chang e in leng th ov er the
temperature interv al u der consideration
within ± 2 %
This dev ice shal not exert a stres of more
than 5 kPa on this specimen which shal not be
distorted or indented
3.2 Sca l e o ca l iper
The s ale or calper shal be ca a le of measuring
the test leng th of the specimen with an ac uracy
of±0,5%
3.3 Tempera ture ba th
The temperature of the specimen shal prefera ly be
controled b the use of a lquid b th The b th shal
be ar ang ed in such a wa that u iform
temperature throug hout the specimen is secured
Means shal be prov ided for stir ing the b th and for
control ng its temperature within ± 0,2 °C of the
temperatures used
4 Specim ens
4.1 Preparation
Specimens shal be cut or sha ed, f om she t The
ends of the specimen shal be cut perpendicular to
the a is of the specimen.They shal be protected b
means of thin ste l plates cemented to them
4.2 Dim ensions
For the a p ratus shown in Fig ure 1, specimens can
be rou d or square and shal fit easi y into the outer
tube without exces iv e pla The leng th of the
specimen ma be 5 mm to 10 mm but its leng th is
g ov erned to some ex tent b the sensitiv ity of the dial
g aug e, the ex ected ex ansion and the desired
ac uracy
5 Conditioning
The specimen shal be conditioned
at ( 23 ± 2) °C, ( 50 ± 5)% relativ e h midity for at
least 4 h prior to measurement of the test leng th of
the specimen u der these conditions
6 Procedure
The temperature range over which the co ficient of
thermal ex ansion is to be measured shal be chosen
so that no transitional reg ions are included
The l mits of the rang e shal be ag re d betwe n
pur haser and manufacturer
6.1 Low temperature
Mou t the specimen in the a p ratus and maintain
the temperature of the b th at the lowest
temperature at which measurements are required
u ti the temperature of the specimen reaches the
temperature of the b th The time neces ary shal
be determined b prelminary measurements of
temperature inside a simiar specimen Record the
rea ing of the dial g aug e or other dev ice indicating
chang e in leng th
6.2 Hig h tem perature
Repeat the foreg oing operations at the hig hest
temperature at which measurements are required
6.3 Che k determ ination
Repeat the operations des ribed in 6.1 and 6.2 I
the chang es in leng th caused b heating and co lng
do not ag re within 10% of their av erag e, the cause
of this dis rep ncy shal be inv estig ated and if
pos ible, elminated ( se 6.5) Otherwise the
observ ations shal be reported, se 8.3
6.4 Constant temperature bath
W here the construction of the a p ratus permits, it
ma be more conv enient to alternately use two
b ths at the required temperatures Care shal be
taken not to disturb the a p ratus during exchang e
The use of two b ths is prefer ed because it wi l
reduce the time required to bring the specimen to
the desired temperature The test in g eneral shal
be conducted in as short a time as pos ible to av oid
chang es in phy sical properties during long ex osure
to high and low temperatures
Trang 86.5 Transition tem perature
The co ficient of thermal ex pansion of some
materials is k own to chang e rather a ruptly at a
certain temperature To find this temperature, it is
neces ary to measure the co ficient of thermal
ex ansion in nar ow temperature l mits, or to
observ e the rate of ex ansion during a stea y rise in
temperature of the specimen Once such a transition
point has be n fou d, a sep rate co ficient of
ex ansion for a temperature rang e below and a ov e
the transition point shal be determined
7 Expres ion ofresults
The av erag e co ficient of thermal ex ansion shal
be calculated fom the formula:
Co ficient of l near thermal ex ansion =
where:
8 Test report
It shal include:
8.1 Temperatures betwe n which the co ficient of
thermal ex ansion has be n computed
8.2 Av erag e co ficient of lnear thermal ex ansion
per °C
8.3 Complete des ription of any u usual behav iour
such as, for instance, a diference of more than 10%
in measured v alues of ex ansion and contraction
% L is the av erag e of chang es in leng th due to
heating or co lng ;
L is the test leng th of specimens immediately
after the conditioning stag e ( %L and L
being in the same u its);
T is the temperature diference in °C ov er
which the chang e in leng th has be n
measured
%L
L T
Trang 9Fig ure 1 — Quartz- tube di atom eter
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