Experimental study on active infrared thermography as a NDI tool for

Composites: Part B 45 (2013) 138–147
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Composites: Part B
journal homepage: www.elsevier.com/locate/compositesb
Experimental study on active infrared thermography as a NDI tool for
carbon–carbon composites
Liu Junyan a,⇑, Liu Liqiang b, Wang Yang a
a
b
School of Mechatronics Engineering, Harbin Institute of Technology, Harbin 150001, PR China
Jiamusi university, Jiamusi 154007, PR China
a r t i c l e
i n f o
Article history:
Received 2 January 2012
012
Received in revised form 14 March 2012
Accepted 1 September 2012
Available online 16 September 2012
Keywords:
C. Finite element analysis
A. Carbon–carbon composites (CCCs)
D. Non-destructive testing
a b s t r a c t
Active
A
Ac
Act
c ive
ve infrared
ve
in
iinf
nffrra
n
rar
arred
a
d thermographic
ther
he
he
errmogr
mo raphic technique
mog
techn
hni
niique
qu
ue was
ue
w used
use
us
u
se
sed as
as a non-destructive
no
on
n-d
n-d
-destructive inspection
in
(NDI) tool for carbon–
car
arrbon
a
bo
b
on (C/C)
(C/
((C
C/
C/C)) composite
comp
o
osite with subsurface
sub
bsur
s face defects.
su
defec
fec
eccts
tts.
s A serial
seri
se
ri l of
ria
o representative
rep
rep
re
epresentative carbon–carbon composite test
carbon
samples,
experimentally
and analyzed using
sam
am
mpl
ple
p
l s,, consisting
consisting
g of cutoutss and
an
a
nd cracks
crracks as defects
defe
efe
fect
ecct
cts
tts were
wer
erre investigated
e
iinves
in
nv
vesstig
t gated
g
exp
finite
element
thermography technique
fini
niitte
ee
lement method
le
met
etth
ho
hod
od
od (FEM).
((F
(FE
FE
F
EM). Both
Bot
B
oth transient
trrans
anssien
i t pulsed
ie
pulse
se
ed thermography
the
errrm
erm
mogr
o aph
ap
phy and
ph
and lock-in
lo
wer
re iin
vestigated. The
The
he capability
capa
ap
ap
pa
ab
bil
illity
ity
y off two
two
o techniques
techniques to
o detect
detect subsurface
subs
bsurrface defects
bs
d
were
investigated.
of C/C composite and to
provide
that active thermographic
pro
ro
ovid
i e information about
ab
abo
bout
bo
ut the
the location
loca
ca
atio
tio
on of
o defect
defect was analyzed.
ana
na
alyz
ly ed.
d. Results
d.
Result
Res
ult
u
ltts indicate
ind
technique
composite.
te
ecchni
e
h que is available for
fo
orr the
the subsurface
subsurf
rfface
acce
a
ce defect
def
d
de
effec
e
ect
e
c detection
d ection
det
on
n of carbon–carbon
carb
arb
arbon
bon–
n–
n
–car
c b
Crown
Ltd. All rights reserved.
Crow
wn Copyright
wn
Co
op
opy
py
pyrri
rig
iight Ó 2012
2 Published
Pu
ubl
bliish
bli
ssh
h
he
ed by
b Elsevier
E
1. Introduction
te
ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
d thermographic
therm
rmog
rm
graph
rra
aph
p icc measurements
me
m
easurrem
men
ents
t and
an
nd
In the last decades, infrared
use
s d in
in the
the
e inspection
iin
nsp
s ection
n of
of subssu
ub
b-investigation techniques have been used
surface defects and features, thermophysical
thermoph
physsic
ph
ical
al properties,
p op
pr
ope
errties, coating
on, and so
o on
on [1
1,,2
2]. D
urin
ur
ing infrared
infrared
thickness and hidden corrosion,
[1,2].
During
ere are two approaches
appr
ap
p roa
oach
chess that
th
hat
at can
can be
ca
be
thermographic inspections, there
approa
acch
h iss generally
ge
g
en
ene
ne
erra
all
lly used
lly
used
se
ed
used: passive and active. The passive approach
at are at different temperature
te
emp
m erat
attur
a
ure comco
com
om
min the research on materials that
ap
pp
pro
r acch,
h an
pare with the ambient, while in the case of active approach,
ch as optical flash lamps, halogen
hallo
loge
gen
external excitation source, such
onic vibration,
vibration hot and cold air gun
heat lamps, mechanical ultrasonic
is employed with the intention of inducing thermal contrast [3–
5]. In the active approach of the infrared thermographic nondestructive testing and evaluation (NDT&E), pulsed transient thermography and lock-in thermography are the most commonly used
approaches.
In pulsed transient thermography, the surface of specimen is
pulsed heated (from ms to s) by different heating sources and
the resulting thermal transient at the surface is monitored using
an infrared camera. The duration of the heating pulse depends on
the thermal and physical properties of the materials, as well as
its thickness [6]. The heat flow into the sample is altered in the
presence of a subsurface defect or feature, creating temperature
contrast at the surface that is recorded by an infrared system [7,8].
⇑ Corresponding author. Tel.: +86 451 8640 3380; fax: +86 451 8640 2755.
E-mail address: [email protected] (L. Junyan).
In
n lo
ock
c -in thermogra
ap
ph
hy,, the
the surface
th
sur
urfac is heated periodically, typlock-in
thermography,
i al
ic
ally
y using
ussing sinusoidally
u
sinusoida
all
lly modulated
mod
dulatted halogen
ha
ically
lamps, and the tempe
era
rature
re
e modulation
on
n induced
indu
in
duce
du
ced at
at the surface of the inspected
perature
comp
mpon
mp
o en
nt from
from
m the
the
he outside
outs
ou
uts
tsid
id
de
e propagates
propaga
component
can be looked as a harmoni
niic thermal
the
erm
r all wave
wa
w
ave
e [9
[[9,10].
9,,1
10].. Thermal
Thermal images of the sample are
monic
reco
orrd
ded
ed throughout
th
hrro
oug
ugho
out
ut the
tth
he heating
heating period,
per
recorded
which lasts for a least
on
ne full
fu
ulll excitation
exc
xcit
itattiio
on cycle.
cyc
y le
l . The
The phase is modified by thermal waves
one
comi
co
m ng back
mi
ba
b
ack
ck from
ffrro
om
m inside
in
nsi
side of the material,
mater
coming
and it can be extracted
by post-analyzing
po
p
ost
stt-a
-a
an
na
aly
lyzing
ng
g the
the recorded images
th
image data [11,12]. The lock-in
by
tth
herrmo
m gr
grap
ap
phy
hy process facilitates a number
num
thermography
of advantages for subssurface
su
urf
rfac
ace defect
defect detection, and experimental
experim
artifacts due to environmental reflections,
reflections local non-uniform
non-unif
emissivity of sample
surface, air turbulence, etc., are significantly reduced [13].
It is an objective of this work to investigate subsurface defect
detection of carbon–carbon composite using both pulse transient
thermography and lock-in thermography. Finite element analysis
and experimentally trails of through skin imaging of subsurface
defect fixtures are presented in this paper.
2. Finite element analysis
In this section, finite element method (FEM) is used to investigate the surface temperature variation of C/C composite specimen
under the pulsed heat and modulation heat excitation conditions.
The incident heat flux function was described on the front face of
C/C composite specimen as following:
(q
q ðx;y;0;tÞ ¼
in
1359-8368/$ - see front matter Crown Copyright Ó 2012 Published by Elsevier Ltd. All rights reserved.
http://dx.doi.org/10.1016/j.compositesb.2012.09.006
A
½1 cosð2pftÞ
2
qmax
½1 signðt t c Þ
2
Lock in thermography
Pulsed thermography
ð1Þ
139
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
with
8
>
< 1 0 6 t < t c
signðt tc Þ ¼ 0
t ¼ tc
>
:
1
t > tc
ð2Þ
where qin(x, y, 0, t) is the incident heat flux function, qA the amplitude of modulated heat flux, f the modulation frequency, qmax the
peak value of pulsed heat flow, and tc is the pulsed heating time.
It is well known that the temperature distribution T(x, y, z, t), in
the considered anisotropic material satisfies the following thermal
conduction partial differential equation [14].
@Tðx;y;z;tÞ
@
@Tðx;y;z;tÞ
kxx ðx;y;zÞ
@t
@x
@x
@
@Tðx;y;z;tÞ
@
@Tðx;y;z;tÞ
þ
þ
¼ 0 ð3Þ
kyy ðx;y;zÞ
kzz ðx;y;zÞ
@y
@y
@z
@z
qðx;y;zÞ cp ðx;y;zÞ
D6
D5
he p
re
ese
sentt investigation, a pulsed
pul
In th
the
present
thermal source and a sinusoid
so
idal
al thermal
the
th
ther
errma
rmall source
sou
ourc
rce were used to excite
e
soidal
the surface of a C/C composi
siite
e specimen
speccim
sp
men
e with
wiith
w
th cutouts on the
t
posite
opposite side, respectively.
Th
he response
res
espo
p nsse of
of thermally
the
the
h rm
rma
allly excited surface was recorded simultaThe
n ously using
ne
ussiing
n an
an infrared
iin
nfrrarred
ed camera. Real
R
neously
time analysis of both signals was
na
w s performed
wa
per
errform
form
fo
med
ed to
t determine
de
de
nals
the associated phase angle
usiin
us
ng available
available lock-in
lock
lo
k--iin modulus.
mod
dul
ulus
lu .
using
Fou
Fo
urr C/C composite
com
mpo
posite specimens
spec
eccim
mens were manufactured. Circular
Four
cu
uto
tout
u s of
of varying
varying depth
de
ept
pth
h and
and
n diameter
diamet were manufactured in specdi
cutouts
en
e
n 1#
1# and
an
a
nd 2#,
2#, and
d specimen
spe
peci
cciime
men 3#
3# and
a 4# were formed SiC coating
imen
n the
the surface
th
su
su
urrface of spec
cim
me
en
n in
in much
m ch higher temperature environmu
on
specimen
ment by chemical vapor
vapo
or reaction
rea
eacttio
ion
on (CVR),
(CV but this method is inclined
ment
o generate cracks in the
th
he specimen.
spe
peci
cime
ci
me
m
en. The idealized shape of a circuto
defect was chosen in
n thiss investigation
invesstig
in
larr defect
to illustrate the effects of
geo
ge
om
metry on observed
ed
d thermal
tth
herrm
ma
al response.
resp
geometry
Fig. 3 shows the geometrry of
of the
the test specim
im
men u
us
sed
e iin
n this
th study. An integrate pulsed
try
specimen
used
the
th
errmo
m graphy and
d lock-in
locckk in
n thermography
therrmogr
th
thermography
system employing a midwave
ele
length infrared
infrar
arred
ed camera
ca
am
me
era (SC7300
(SC73
wavelength
2.5–5.0 lm with internal
lo
ock
c -in
n unit
unit by
y FLIR
FL
LIIR ATS)
AT
TS
S) were
we
erre utilized
utiliz for the experimental work.
lock-in
Th
he sschematic
ch
hem
e attiicc of
of general
ge
g
enera
ne
n
er l test
test arrangement
arran
The
is presented in Fig. 4,
an
nd tthe
he in
he
nfr
frar
ared thermographic
th
her
ermogr
ogr
g aphic system
syst
and
infrared
is a portable non-destructive
evaluation
tiv
ti
ve ev
va
allua
uatiio
on
n system
syst
sy
stem
m with
w th a flash heat device and a modulation
wi
h
he
eat
a exci
ciita
attiiion
on
o
n apparatus.
appa
ap
paratus. The flash heat device used an pulse elecpa
heat
excitation
ttr
ric
ic power
po
p
ow
we
er to
to provide
pro
rovide power output
outpu 4.6 KJ in 2–5 ms from lamp,
tric
a
nd a tr
trig
ig
gg
ge
er was used to control the flash lamp switch, which
and
trigger
e
en
na
ab
blle
es the infrared camera to simultaneously
simu
enables
record the response
of thermally excited surface at the beginning of pulsed thermal
excitation. The modulation heat apparatus used two 1 KW halogen
lamps to provide the thermal excitation, and a Protek 9031 function generator was used to control the amplifier to sinusoidally
modulate the intensity of the lamps. To prevent direct reflection
back into the infrared camera, the thermal sources were oriented
D7
D3
D4
3. Experiments
ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
where q(x, y, z) is the density
ty in the domain, cp(x, y, z) the specific
condu
du
d
uccttiiv
vit
ity in
in
heat capacity of material, kd(x, y, z) is the thermal conductivity
the domain (d = xx, yy, zz).
If the initial temperature distribution of dom
domain
om
o
mai
mai
ain considered
co
on
nsi
sidere
dered
de
re
ed and
an
nd
d
ditions (heat flux,
flux
ux, continuity
c nttiin
con
nu
u
uit
iitty and
and
nd insui suin
the necessary boundary conditions
3) will be solved.
sso
ollv
ved
d. However,
H
How
ow
o
we
ev
ver
er,, Eq.
Eq. (3) is
i
lation) are presented, Eq. (3)
lytical solution
solu
llu
uti
tion
n due
due to
du
to specimen
spe
peci
c men struchardly solved using the analytical
earizatio
on boundary
bou
und
ndar
ary
y and
and anisotropic
an
nissot
otro
r pic
ture complicated, non-linearization
or C/C composite.
cco
omp
m ositte. The
The commercially
Th
comme
errccia
iall
lly fifithermophysical properties for
softtw
wa
are
r , COMSOL
COM
MS
SO
OL Multiphysics
Multiphyssic
ics was
wa
ass
nite element analysis (FEA) software,
or of
of thermal
therrma
th
m l response
response of C/C composco
omp
pos
o selected to study the behavior
ation
on
o
n heat
heat
he
at excitation
ex
xcitation conditions.. The
The
h
ite under pulse and modulation
COM
MS
SO
OL was
was applied to simulate
e the
the
e
heat transfer modulus of COMSOL
tin
ng problems
pro
rob
bllem
ems where
where surface temperatem
mperathermal non-destructive testing
ace
e features
feat
fe
atur
at
ures
ur
ess (i.e.
(i.e. defects, damages
damag
ag
ges and
ture signals include subsurface
y interest.
in
ntere
rest
re
st. It
It is
is intended
intended forr calculating
ca
alc
lculating
discontinuity) are of primary
an anisotropic
ani
niso
s tr
tro
op
pic thermophysical
thermoph
ph
p
hysical solid
3D temperature distribution in an
e defects
de
efe
fect
ctts or
or features.
fea
eat res. The
eatu
e heat
heat transfer
that may contain subsurface
ing of
of thin
th
hiin subsurface
sub
bsurface features,
fe
ea
e
atu
ture
r s, which
modulus enables the modeling
eated
d uniformly
uniifo
forrm
mly
y or
or non-uniformly
n n-un
no
un
niiffor
orm
mly
y with
wit
ih
allows the specimen to be heated
ction description
des
e crrip
iption
tion
ti
n [15].
[[1
15].
a random mathematical function
osite whose
wh
w
hos
ose
e dimensional
d
dim
i e
im
en
nssiiional size
siize was
w s
wa
A solid of C/C composite
ussed
d ass the
the geometry
th
geo
eom
me
etr
etr
try model,
80 mm 40 mm 9.2 mm was used
T e defect
Th
de
effe
ecct depth
dep
pth
th refers
rre
efe
fers
rs to
which consists of different size defects. The
und surface and
nd
d the
t e top
th
top
p face
ffa
ace
ce of defect.
de
d
effe
ecctt.
the distance between the sound
om 0.5 mm to 4.0 mm,
mm, and
mm
and
nd the
the defect
th
de
effec
e t
The defect depth varied from
re and
re
an
a
nd meshing
mes
mes
eshi
hiing
h
ng
thickness is set up 0.1 mm. The geometry structure
t p are
are
re dididi
grid were shown in Fig. 1. The meshing size and time-ste
time-step
ergence and stability of thermal model
rectly influence on the convergence
solution by COMOSL heat transfer modulus. For given geometry
model in Fig. 1a, the automatically meshing was hardly implemented to mesh successfully, the swept meshing method was used
to mesh the geometry model, and the geometry model meshing
process was presented in Fig. 2. The choosing time-step was de-
pended on the analysis time and sample frames. For pulsed transient thermography, the time-step was set to 0.02 s for the
simulation on the duration of 5.0 s. For lock-in thermography,
the time-step was determined by the modulation frequency and
analysis periods, and it was set to 2.0/(100 f). So, the above
appropriate meshing size and time-step choosing, whish ensured
the convergence and stability of thermal model solution. The thermophysical parameters C/C composite were measured experimentally, which the test specimen was manufactured as a round shape
(diameters 12.5 mm and thickness 2.5 mm) and the Netzsch
LFA457 made in Germany was used to measure the thermophysical parameters of different directions in the temperature range
from room temperature to 1000 °C. The thermophysical parameters shown in Table 1 and simulation parameters shown in Table
2 were used for the finite element analysis.
D2
te
D1
80
40
(a)
(b)
Fig. 1. The geometry structure and finite element grid: (a) geometry structure and (b) finite element meshing grid.
140
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
Top layer solid
Dividing
Defective layer solid
Swept meshing:
1. Number of element layers
2. Meshing size (extra-fine,
finer, fine, normal, coarse,
coarser, and extra-coarse)
Y
Matching
Close?
N
Bottom layer solid
Fig. 2. The meshing grid process and matching.
Table 1
Thermophysical parameters used during
ng modeling.
Component
C/C composite
Air
Parameter
m3)
Density q (kg/m
Special
Sp
pec
eci
cciia
all heat
heat
att c (J/(kg°C))
(J/
(J
JJ///(kg
(kg
((k
kg°C))
k
C)))
1955
1.1774
19
1
900
1900
1005.3
Thermal diffusivity
d
a 106 (m2/s)
Thermal
h
conductivit
conductivity
vit
itty k (W/
((W/(m
/(m
(m °C))
°C))
C)))
))
x
y
z
x
y
z
60
60
60
60
0.
..0
026
0.026
45
1
16.2
16.2
21.9
12.1
Table 2
Simulation parameters used during modeling.
odellliing.
Pulse transient thermography
Lo
L
Lock-in
occk-in thermogr
o
thermography
ra
ap
phy
p
Heat time (s)
End time (s)
s)
Time
T m step (s)
Tim
Modulation
Mod
M
ulation fr
ffrequency
re en
requ
nccy (Hz)
n
Analysis
periods
number
Analys
lys
yssis p
y
eriods
eri
o n
um
Sample numbers
0.002
0.003
5.0
5.0
0.
0.0
.0
02
0.02
0.0
02
0.02
0.05, 0.10, 0
0.
.15
5
0.15
0.20, 0.50, 0
.08
8, 1.
8,
..0
0
0.08,
1.0
2
100
int
nto friction
fri
r ctio
on such
suc
u h as
as cracks,
cra
acks, delamination,
del
ted into
and disbonding
In this
thi
hiss study,
stu
tud
dy
y, the
the
he ultrasound
ultras
asound wave
as
wav stimulation whose modu[17].. In
on
n frequencies
freq
eq
qu
ue
enc
ncie
ie
es were
w
wer
ere varied
er
varied from 0.5
0. down to 0.08 Hz was used
lation
to detect
de
d
ete
tect
e cracks
crracks
accks
a
ks of
of specimen
sp
pec
ecimen 3# and 4#,
4 and the infrared camera
to
wa
w
as used
usse
use
ed to
to record
rec
e orrd the
the surface temperature
tempe
was
with the frame rate
of 37
37 ffr
ram
ames
ess//ss during
during the acquisition duration of 2 modulation
of
frames/s
pe
p
eri
riod
ods.
periods.
te
ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
on either side of the specimen.. The inf
infrared
nfra
nf
r re
ed camera
cam
amer
erra
er
a uses
uses a cooled
c olled
co
witth a focal
foca
fo
cal plane
pla
ane
ne array
a ra
ar
ay pixel
InSb detector array producing image with
d has a quoted
quote
te
ed thermal
the
herm
rmal
rmal
a sensitivity
se
ens
nsiittiv
iviitty of
of
format of 320 (H) 256 (V) and
re over 25 °C. A sstandard
tand
ta
nda
nd
arrd 50
50 mm
mm fofooless than 25 mK for temperature
investigat
attio
on with
wit
ith the
the
he camcca
ammcus length lens was used in the current investigation
enco
omp
mpassi
as ing
as
g the
the
th
era positioned to fully utilize the field of view encompassing
ples were positioned vertically
verticall
lly with
ll
wit
ith
entire specimen. The test samples
the sound side of the plate exposed to the stimulation source.
For pulsed transient thermography, the heating time was set to
0.003 s, and the infrared camera frame rate was set to 59 frames/
s for the duration time of 5 s. For lock-in thermography, a range
of modulation frequencies was used to interrogate C/C composite
samples ranging from 0.2 Hz down to 0.05 Hz. The infrared camera
frame rate was set to 47 frames/s with 2 numbers of modulated
periods (acquisition time) for each frequency roughly.
In this study, the ultrasound lock-in thermography (ULIT) was
used to inspect the test specimen 3# and 4#, the external excitation is provided by an ultrasonic wave transducer (sonotrode) of
19.8 kHz resonance frequency drive by a specific amplifier/function generator, and Fig. 5 illustrates the experimental setup. The
sonotrode was directly positioned on the edge of specimen, rigidly
coupled to the sample, and as far as possible contact with the edge
by an air cylinder. The maximum output power of PZTs is about
1.5 KW, and it produced ultrasounds wave within sample in this
case of experimental investigation, which would create local friction between the defect edges, those would be converted into heat
sources detectable by the infrared camera [16]. This mechanism
concerns only certain defects involving edges that can be submit-
4. Results
4.1. Pulsed transient thermography
In this section, only the surface temperature contrast was used
to investigate the defect detectability using pulsed transient thermography. The surface temperature difference DT(x, y, 0, s) at each
pixel of thermal image between defective area and the healthy area
was defined by Eq. (4.a) and its normalization DT(x, y, 0, s)N was
defined by Eq. (4.b).
DTðx; y; 0; sÞ ¼ T d ðx; y; 0; sÞ T h ðx; y; 0; sÞ
DTðx; y; 0; sÞN ¼
fmax½DTðx; y; 0; sÞ DTðx; y; 0; sÞg
fDTðx; y; 0; sÞ min½DTðx; y; 0; sÞg
ð4:aÞ
ð4:bÞ
where T(x, y, 0, s)d is the temperature of pixel (x, y) of the defective
area and T(x, y, 0, s)h is the temperature of pixel (x, y) of the healthy
area.
141
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
8
80
10
100
50
80
4×Φ6
4×Φ3
4
3
1.2
1.0
1.2
1.5
1
4×Φ1
2
10
3×Φ6
((a))
((b))
10
80
80
80
8
8
80
80
(c)
(d)
Fig.
Fig
ig
g. 3.
3. Geometry
Geo
eo
e
omet
m ry
y structu
structure
ure
e of
of C/C
/ composite
p
e sp
specimens:
p cciime
pec
men
m
e s:: (a)
( ) 1#,, (b)
( ) 2#,, (c)
( )3
3#
# and
an
nd ((d
(d)
d) 4#.
4#
#.
Fuunc
ncti
tion Generator
Gen
ner
e at
ator aand
nndd Power
Pooow
werr Amplifier
Amppliifi
f er
Function
Puls
se el
eelectric
lec
e tr
tric
ic ppower
ow
wer
Pulse
Infrared
ared Camera and In
IInternal
nte
t rnal
all
Lock-in Unit
Test specimen
Modulated excitation source
ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
Pulse excitation source
Sim
Si
muuult
ltaan
ltan
neo
neo
eous Trigger
Tri
rigg
gger
gg
Simultaneous
Acquisition and analysis system
Fig. 4. A schematic of the experimental arrangement used to perform both lock-in thermography and pulsed transient thermography.
te
The temperature variation curve of FEM and experimental measurement during pulsed heating time of 0.003 s are plotted in
Fig. 6.
Fig. 6a plots the curve of surface temperature variation with
time. Also, Fig. 6b plots the curve of the logarithmic value of temperature log10 (T) with the logarithmic value of the time. It is found
that the surface temperature of FEM is in good agreement with the
experimental measurements, especially, during the duration of 1 s
after the pulse flash excitation. However, over the time of 1 s after
the pulse flash excitation, the surface temperature is reduced to a
constant value due to the cooling course. Thus indicates that in this
presented investigation, the FEA by COMSOL heat transfer modulus
is available for being allowed to investigate the behavior of thermal
response of C/C composite using pulsed heat excitation. The tem-
142
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
Amplifier/ function generator
PZTs
Sonotrode
Air cylinder
Reference sample
Infrared camera
Trigger
Inner lock-in unit
PC
Fig. 5. Experimental set-up
set-up
up
u
p fo
ffor
o
orr ult
u
ultrasound
ltras
rassound
ra
rasoun
oun
oun
und llo
lock-in
ock
ck-in
in thermography.
Fig. 6. Simulations of temperature contrast
ntrast a
and
nd
de
experimental
xpe
x
xp
p
pe
erim
men
ent
ntta
n
al measurements
meassur
ure
u
rremen
ments ffor
orr defect
o
d ect
defe
ct d
depth
ep
ptth off 1.0
p
1.0 mm: (a) temperature
tem
mp
per
pe
eratu
e
ure
e contrast
cont
ontrrras
a t and (b) the logarithm of temperature
contrast.
Th
he gray
gra
ay scale
sca
calle
e of each
eacch
ea
h image
im
mage has been adjusted to maximize
The
conttra
rast between
be
etw
we
ee
en the
the
he defect
defe
de
ect
ct and the sound
so
contrast
material. In Fig. 8a, capttu
ure
red the
red
the
he temperature
temp
mp
pe
errat
atu
urre contrast
contrast image at the time of 0.017 s, detured
fectts are
are
re not
not observed
no
obse
errved at all. While
Wh
fects
the recording time is
increa
in
crea
cr
ase
sed to
to 0.067
0.0
0.0
06
67
7 s, the defects at the
th depth of 1.0 mm are obincreased
e in
n Fig.
Fiig. 8b. The captured time of infrared camera is increased
F
served
to 0.101
0.101 s, the defects at the depths of 1.0 mm and 2.0 mm become
to
i ibl as shown
h
i Fig.
Fi 8c
8 and
d d.
d However, the defect depth
visible,
in
reaches up to 3.0 mm, the defect that the size is diameter
3.0 mm is unable to be detected due to very small temperature
contrast from Fig. 8c and d, and this presents in agreement with
the FEM results. In this study, the temperature contrast image is
only applied to detect the subsurface defects of C/C composite,
and the temperature data can be analyzed by Fourier transformation (Phase Pulse Thermography-PPT) method [18], Thermal Wave
Signal Reconstruction (TSR) method [19], etc., which have been
shown to produce deeper defect detection limits.
The temperature contrast at the sample surface provides sufficient information about the shape and location of subsurface
defect, and the boundary of the defect results in maximum
and minimum temperature changes that help determine its size
and location. The slope curve of the normalized temperature
contrast distribution can be obtained by means of the differential calculation along the x or y axis, where the differential normalized temperature contrast DDT(x, y, 0, s) in Eq. (5) is
calculated by subtraction of adjacent normalized temperature
contrast.
te
ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
perature and its logarithmic value
lue at the
e time
tim
me of
of 0.1
0.1
1 s provide
pro
r vide maximum difference between defective
ctive region
n and
and healthy
hea
alt
lthy
hy
y region
regi
re
gion
o from
Fig. 6, and this record time is suggested
uggested to detect
de
ettecct the
th
he
e defect
de
d
efe
ectt of
of C/C
C/C
C/
composite using the surface temperature
mperature image
e of
o pulsed
pu
puls
uls
lssed
ed
e
d transient
ttrra
an
nssiien
entt
thermography.
func
fu
n ttiion
The temperature contrast off FEA over the defects as a function
sed excitation time of 0.002 s and
d
of defect depth with the pulsed
0.003 s are illustrated in Fig. 7.
It can be seen form Fig. 7, the temperature contrast is decreased
in an almost exponential manner with defect depth increasing. As
we all known that the thermal sensitivity of infrared camera is
about 0.025 °C for environment temperature about 25 °C, and we
can use this value to estimate the limit of defect depth detectability using pulsed transient thermography for the heating time of
0.002 s and 0.003 s. We assume that the temperature contrast between defective area and healthy area is over two times of thermal
sensitivity of infrared camera, and then the defect is allowed to detect by the temperature contrast image. When the defect depth
reached up 2.0 mm, the temperature contrasts over all size defects
are below the 0.05 °C, and these defects cannot be detected using
temperature contrast image with pulsed heating time of 0.002 s
from Fig. 7a. While, the defects whose size are over the diameter
3.0 at the defect depth of 2.0 mm are detectable using the temperature contrast image with pulsed heat time of 0.003 s from Fig. 7b.
Fig. 8 shows the specimen 2# examples using the temperature
contrast image at the record time of 0.017 s, 0.067 s, 0.083 s and
0.101 s.
143
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
Fig. 7. Simulations of temperature contrast as a function of the defect depth: (a) pulsed heating time of 0.002 s and (b) pulsed heating time of 0.003 s.
Fig. 8. Temperature contrast image
mage of p
pulsed
uls
u
ul
llsed tther
thermography
her
errmog
mog
gra
gr
rrap
a hy with p
pu
pul
pulsed
ulsed
ul
sed
se
ed heatin
heating
ng ti
time
me
eo
off 0.
0
0.003
.0
.003
003
0 s at the
he
e tim
time
e of
o
of:
f: ((a
f:
(a)) 0.
0
0.017
.01
17 s, (b) 0
0.067 s, (c) 0.083 s and (d) 0.101 s.
DDTðx; y; 0; sÞN jx ¼ DTðx þ 1;; y; 0;
0; sÞN DTð
Tðx;
ðx; y; 0; sÞN
ðð5Þ
5Þ
4.2.
4.2
4.
2. Lock-in thermography
thermograph
ph
p
hy
In this following ssection,
ection
ec
n, tthe
e phase
pha angle contrast was used to
In
in
nv
ve
est
stigate the defect
defe
ecctt detectability
de
ette
ect
ctab
bility using lock-in thermography.
investigate
x, y) at each pixel of thermal image
T
Th
he p
h se angle difference
ha
dif
iffffe
erencce Du((x,
The
phase
b
be
etw
wee
een defective
ve
e area
arrea
a
a and
and the
an
the healthy
he
between
area was defined by Eq.
(6
6.a
. ) and
an
nd iits
ts normalization
no
orm
rma
ma
alliz
izat
atio
at
atio
ion Du(x, y)N was defined by Eq. (6.b).
(6.a)
Duððx;
x; yÞÞ ¼ ud ððx;
x; y
yÞÞ uh ððx;
x; yÞ
ffmax½
ma
m
ax½Duððx;
x; yÞ Duðx; yÞg
fDuððx;
x; yÞ min½Duðx; yÞg
y
ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
The differential normalized tem
temperature
mpe
pera
rattu
ure co
ur
ccontrast
ontrast distribution
on
np
pr
proro
o-vides maximum, minimum and
zeros
values,
dz
erros
os v
a ues, the distance between
alu
be
ettw
ween
characteristic points (maximum
value
and
value)
used
mum
m val
lue a
nd
d minimum value
e) iiss u
sed
for defect size determination
and
zero
n an
nd tthe
he ze
he
z
ro
o point is used ffor
or location
or
lo
of defect determination. Fig. 9a
a shows
sho
ows
ws the
th
he normalized
normalize
ed temperature
tem
emperature
eat ttime
ime
eo
off 0.
0
003 s at the
003
00
e ccentral
entral line of
contrast induced by pulse heat
0.003
ers ar
a
re 6
..0
0 mm
m and 3.0
0m
mm
m (seen in
the defects whose diameters
are
6.0
ons ca
an be
an
be d
de
ete
errm
min
i ed fr
rom
om th
he m
axiax
Fig. 8d). Although the locations
can
determined
from
the
maxiure cont
nttra
r stt (s
((seen
see
e n in
in Fig. 9a),
9a)
a), it
it is
is diffidif
iffi
fi-mum normalized temperature
contrast
ct size. The
Th
he differential
diifffe
ere
rent
ntial normalized
normaliized
cult to evaluate the defect
db
yE
q.. (5)
q
((5
5) calculation
c lccul
ca
ula
attio
ion is illustemperature contrast profile obtained
by
Eq.
tions of defects
defe
fe
ecctts can
ca
an
n be
be quantitatively
qu
quan
uan
anttiita
tati
tive
vely
y
trated in Fig. 9b. The locations
oints from Fig. 9b.
9b.
b For
For the
the
he size
siz
si
ze
e of diamdiam
di
amdetermined by zero value points
an
nd 3.0
3.0 mm
mm deep,
de
de
eep
ep, the
ep
the
he
eter 6.0 mm defects that are 1.0 mm, 2.0 mm and
ated to be 20.14 mm, 44.54
44
4
4..5
54 mm
m and
and
d
location of defect is calculated
e of the specimen 2#, and for the
the size
th
siz
iz e
66.45 mm from the left edge
1 0 mm,
mm and 2.0
2 0 mm deep,
deep
of diameter 3.0 mm defectss that are 1.0
the location of defect is calculated to be 20.14 mm and 44.75 from
the left
lef
e t edge
edg
dge of the
e specimen.
ssp
peccim
men
en.. The
The
h distance
d
the
between the maximum
d minimum
min
inim
inim
imum
um differential
differe
en
e
nti
t al
al n
no
orm
malize temperature contrast is caland
normalized
cu
ulla
ate
ted as
as the
the
h size of the
the defect,
de
effect
ectt,, which
ec
whi has been marked in Fig. 9b.
culated
Duððx;
x; y
yÞÞN ¼
ð6:aÞ
ð6:bÞ
te
where u((x,
x, y)
y)d is the phase angle of pixel
p
(x, y) of the defective area
pi
(x, y) of the healthy area.
a
an
nd u(x, y)h is the phase angle of pixel
and
Fig. 10 shows the phase angle contrast
Fig
c
of FEM calculation as
function of modulation excitation frequencies for the size of diam-
Fig. 9. Temperature contrast normalized and its differential curve: (a) the curve of temperature contrast normalized and (b) the differential curve of temperature contrast
normalized.
144
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
observed that the edges of the defect become increasing more diffuse as the defects become deeper, and this is similar to the observation of metal specimen inspection using lock-in thermography
by Wallbrink et al. [20].
The present phase angle measurements have an associated level
of background noise that will interfere with the detection of defects. The ability to detect a defect requires that the phase angle
change caused by the defect is greater than the background noise.
A limitation criterion was proposed in Ref. [20], and we used it to
analyze the detectability of defect using lock-in thermography. Eq.
(7) sets a limitation criterion on the detectability of defects associated with phase angle contrast measurements, where DL represents the limiting phase angle contrast, and two times standard
deviations of phase angle in the defective region and the healthy
region were used to represent 95% confidence intervals for measurements of phase angle contrast in the sound material and over
the defects.
DL ¼ 2rD þ 2rH
DL
ð7Þ
where
wh
w
he
erre rD is
i the
the standard
th
sta
tand
n ard deviation of phase
p
in the defective region,
the
he standard
sta
tand
nda
nd
arrd deviation
deviation of phase
ph
in the healthy region.
an
a
nd rH iss tth
and
When
W
Wh
en
n the
the local
th
lloc
occal phase
o
ph
has
ase angle
angle contrast
contr
over a defect is greater
than DL,
DLL, then
th
he
en a defect
de
efe
fect is
fect
is detected
d tected and
de
an below DL a defect is not
detectable.
Fig.
detectability of dede
ete
tectable. Fi
ig
g.. 14
4 represents
rre
ep
prres
e en
nts
ts experimentally
experim
ffects
fe
ectts with
wiitth various
vario
ouss defect
de
efe
fect
ct depths
dep
de
pths
pt
h using DL as the detectable phase
angle
an
a
ng
glle ccontrast.
on
ntr
t ast.
IIn
n Fig.
Fiig.
F
g 14a, for the
e si
ssize
z off diameter
ze
diam
di
ameter 6.0 mm and 3.0 mm defects,
am
the ph
hase
ha
se angle
angl
an
g e contrast
contras
asst is
is over
ov
ve
er the
the
he DL where the defect depth is by
phase
3.0 m
m a
he
h
e m
odulati
tiion
o ffr
rreq
eq
que
ency of 0.05 Hz, which indicates
mm
att tthe
modulation
frequency
tthat
th
hat the
tth
he size
size of
of diameter
diamete
te
er 6.0
6.0
0 mm
mm and
an 3.0 mm defects that are
3
.0 m
m deep are detec
ctab
ble
le at the
the modulation frequency of
3.0
mm
detectable
0.05
5 Hz.
H . In Fig. 14b, for tthe
Hz
he size
he
i off di
diameter 6.0 mm defects, the
phase
ph
e angle
angle contrast is over
over the
ov
tth
he DLL w
phase
where the defect depth is by
3..0 m
ma
on
o
n fr
ffrequency
eque
eq
uenccy o
3.0
mm
att the modulation
off 0.1 Hz, for the size of diame er 3.0
et
3.0 mm
3.
mm defects, the
he
e phase
phase
asse angle
a
ang
gle contrast
co
eter
is over the DL where
the
th
e d
efe
ef
ecct depth is by
by 2.0
0 mm
mm at
at the
th modulation frequency of
defect
0
0.
1H
z, which
wh
w
hich indicates
indiccat
ate
ess that
th
hat
at the
the size
size of diameter 6.0 mm defects
0.1
Hz,
thatt are
arre 3.0
a
3.0
. mm deep
de
d
eep
ep and
an
nd the
th
he
e size
ssiize of diameter
d
3.0 mm defects that
are 2
.0
0 mm
m de
eep
ep ar
a
re
e d
etteccta
e
able at th
2.0
deep
are
detectable
the modulation frequency of
0.1 H
z. T
he d
ettec
e
e ta
ab
biilliitty
y off defect will
wil change depending on the
Hz.
The
detectability
m
mo
od
du
ula
attiio
on
n frequency,
freq
fr
eq
e
que
uen
nccy,
y hence,
h nce, the number
he
num
modulation
and size of the defects
d
ete
ectted
d will
willll also
wi
allsso
a
o change.
ch
han
a ge.
detected
T
Th
he phase
ph
ha
ase
s angle
an
ng
glle contrast
contrast at the sample
sam
The
surface contains more
iinformation
in
formatio
io
on a
bout the shape and location
loc
about
of subsurface defect.
T
Th
he sslope
lope curve of the normalized phase
ph
The
angle contrast distribution can be obtained by means of the differential
d
calculation along
the x or y axis, where the differential normalized phase angle con-
te
ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
eter 6.0 mm and 3.0 mm defects that the defect depths are different, and it can be used to select an appropriate frequency to provide the largest phase difference for NDI purpose. Frequencies at
which the phase difference becomes zero are known as ‘‘blind frequencies’’, also, the excitation frequency should be selected less
than 0.2 Hz, which is inclined to make more defects be detectable
from Fig. 10. The modulation excitation frequency of 0.1 Hz can be
used to obtain the largest phase angle contrast that the defect
depth is below 1.5 mm, and the excitation frequency of 0.05 Hz
is selected to provide larger phase angle difference that the defect
depth is over 1.5 mm in this experimental investigation.
The phase angle images of the specimen acquired using modulation excitation frequencies of 0.02 Hz, 0.05 Hz, 0.1 Hz and
0.15 Hz are presented in Fig. 11.
The gray scale of each image has been adjusted to the maximize
contrast between the defect and the sound material, and the specimen in Fig. 11 was oriented as in Fig. 4.
In Fig. 11a and b, recorded with modulation excitation frequenhree defects of cutouts orien
ntte
ed are
are
re
cies of 0.02 Hz and 0.05 Hz, three
oriented
th
he vertical
ve
errttiica
cal edge
edg
ge
clearly observed, but for four defects located on the
nd
db
b.. A
he exc
e
xciitta
xc
a-of specimen 1# are not visible from Fig. 11a and
Ass th
the
excitadefeccttss of
of specimen
sp
pe
ecciim
men
en 1#
1# bebe
b
etion frequency is increased to 0.1 Hz, all defects
on frequency
cy increasing,
cy
iin
ncrrea
easing
sin
si
ng
g, the
th
he
e defects
de
d
effe
ectts
ect
come visible. With the excitation
nable to be
be detected
det
etec
ecctte
e
ed in
in Fi
F
ig. 11d. As
located the vertical edge are unable
Fig.
d on the
e v
e ti
er
tica
cca
a
all e
dg
ge o
the size of defect that located
vertical
edge
off specimen
zontall a
xis is onl
xi
nly 1
nl
.0 mm, itt iiss lless
ess
es
1# (seen in Fig. 2a) along horizontal
axis
only
1.0
0 to 1.5
1.5
5 mm,
m , and
mm
d this
th leads to more
more
than the defect depth from 1.0
g horizontal
ho
orriizo
zont
nttal axis
n
ax
xis due to the lower
lo
owe
wer
lateral thermal diffusion along
gener
erat
er
ates
es very
ve
v
ery
y small
small phase angle difdif
ifmodulation frequency, which generates
a and
nd healthy
nd
he
h
ea
allth
thy area.
area. So there exits an
an
ference between defective area
0..1 Hz
0
Hz to
to obtain
obtain the best phase
e anann
optimal excitation frequency off 0.1
sp
pecim
eccim
imen
en 1#
1# using lock-in thermother
errmogle contrast for C/C composite specimen
graphic technique.
A over
ov
ver
er the
t e defects
th
d
fu
un
nct
ction of
The phase angle contrast of FEA
as a function
n frequencies
frreq
e ue
en
nccie
es of
of 0.05 Hz
z and
and 0.1 Hz
defect depth at the modulation
are shown in Fig. 12.
e rate
e at
a wh
w
whic
hic
i h the
th
he
e phase
e angle
ang
ngle conco
onn
As can be seen in Fig. 12, the
which
h decrea
ea
e
ase
s s iin
na
n almost
alm
lmost exponential
exp
xp
pon
onen
e tiial
al
trast is affected by defect depth
decreases
an
cimen 2#
2# examples
ex
xam
ampl
p ess using
using phase
us
s anan
manner. Fig. 13 shows the specimen
n excitation
excitatiion
on frequencies
frreq
eque
uenc
ncie
ies of
ie
of 0.15
0
gle images at the modulation
Hz,
0.1 Hz and 0.05 Hz.
he modulation
n ffrequency
r quen
re
qu
uen
ency
cy of
of 0.
0
15
1
5 Hz
H
z,
In Fig. 13a, acquired with the
0.15
Hz,
he modulation
he
m du
mo
dulla
attiion
on frefrefr
edefects that are 1.0 mm deep are observed. As the
.1 Hz, defects that are
e 1.0
1..0 mm
1
mm and
an
nd
d
quency is decreased to the 0.1
ajor
aj
orit
ity
2.0 mm deep become visible, as shown in Fig. 13b. The m
majority
of the defects are detectable in Fig. 13c, which was recorded at
the modulation frequency of 0.05 Hz. However, in Fig. 13, we also
Fig. 10. Phase contrast as function of thermal excitation frequency: (a) the 6.0 mm diameter blind holes and (b) the 3.0 mm diameter blind holes.
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
145
Fig. 11. Phase angle image of specimen 1# recorded at the modulation frequencies of (a) 0.02 Hz, (b) 0.05 Hz, (c) 0.1 Hz and (d) 0.15 Hz.
Fig. 12. Simulations of phase
se ang
angle
ng
n
g
gllle
e ccon
contrast
on
ntras
nt
ra
ast a
ass a function of the defe
defect
efect
ecctt depth:
depth: (a) m
modulation
mo
od
odu
o
d
du
ulat
lat
atiio
ion
on
o
n frequency of
of 0.05
0.05
05
5H
Hz
z and
an
nd
d (b)
(b) modulation
m
frequency of 0.1 Hz.
ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
Fig. 13. Phase angle
le
e contra
co
contrast
t ast
ast ima
as
image
ma
m
ag
ge
eo
off th
tthe
he ssp
speci
specimen
ecimen
en 2#
2# rrecorded
ecorrde
ecorde
eco
rde
rd
ded
d
ed a
at the
t e mod
m
modulation
odula
ua
atttiiio
on
n frequen
frequenc
frequencies
enc
nciie
nc
ies
ess of:
e
f:: (a)
((a
a) 0.1
a)
0.
0
0.15
5 Hz
H
Hz,, (b) 0
0.1 Hz and (c) 0.05 Hz.
Fig. 14. Phase angle contrast of specimen #2 for defect diameter 6.0 mm and 3.0 mm as a function of defect depth at the modulation frequencies of: (a) 0.05 Hz and (b) 0.1 Hz.
DDuðx; yÞN jx ¼ Duðx þ 1; yÞN Duðx; yÞN
te
trast DDu(x, y, 0, s) in Eq. (8) is calculated by subtraction of adjacent normalized phase angle contrast.
ð8Þ
The differential normalized phase angle contrast distribution provides maximum, minimum and zeros values, too. The distance between characteristic points is used for defect size determination
and the zero point is used for location of defect determination.
Fig. 15a shows the normalized phase angle contrast induced by
the modulation frequency of 0.05 Hz at the central line of the defects whose diameters are 6.0 mm and 3.0 mm (seen in Fig. 13c).
The locations of defects can be quantitatively determined by zero
value points from Fig. 15b. The location of diameter 6.0 mm defects
that are 1.0 mm, 2.0 mm and 3.0 mm deep is calculated to be
20.04 mm, 43.24 mm and 66.8 mm from the left edge of the specimen 2#, and the location of diameter 3.0 mm defects that are
146
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
Fig. 15. Phase angle contrast normalized and its differential curve: (a) the curve of phase angle contrast normalized and (b) the differential curve of phase angle contrast
normalized.
Fig. 16. Phase angle image off spec
specimen
pec
p
eccime
e
im
men 3
me
3#
# us
using
siing
ng ultrasound
u t asou d lock-in
oc n th
thermography
herrrm
mo
ogr
og
g
gra
aph
ap
phy att the
tth
he m
he
modula
mo
mod
modulation
od
o
dula
ul tion
t o frequen
frequencies
equen
nccies
iess of
of ((a)
a) 0
a)
0.1
.1
1H
Hz,
z (b) 0.2 Hz and (c) 0.5 Hz.
1.0 mm, 2.0 mm and 3.0 mm dee
deep
ep is calcu
calculated
cula
cu
l ted to be 20.04
04
4 mm,
ft e
d eo
dg
he
e sp
sspecimen.
ecimen. The
he di
d
istance
44.65 and 67.9 mm from the left
edge
off tthe
distance
between the minimum and ma
maximum
differential
normalized
axi
x mu
mum
um d
di
ifferential n
ormalized
ated a
he ssize
iz
ze o
efe
ect
c , which
phase angle contrast is calculated
ass tth
the
off the de
defect,
has been marked in Fig. 15b.
4.3. Ultrasound lock-in thermography
raphy
juD uH j
rHu
ð9Þ
where
wh
her
ere
e SNR
SSN
NR presents th
the
he ssignal–noise
ig
gna
al–no
oise ratio in phase angle image,
wh
whe
here uD and uH are
e tthe
he
h
em
me
mean
ea
an
n va
value
alue of phase in the defective areas
where
presents
pr
resen
en
e
nts the standard deviation of phase
healthy
and
and
d healt
h
thy
h areas,
s,, an
a
nd rHu p
nd
angl
le iin
nh
ea
e
althy
hy
y ar
a
rea
eas,, re
rrespectively.
esp
s eccti
tively.
angle
healthy
areas,
The
Th
he phase
pha
ase
se angle
angl
an
g e images
im
ma
ages of
of specimen
specime 3# by ULIT are illustrated
Fig
Fi
g. 16(a–c).
16
6(a
(a–cc).. In
In the
tth
he same
sam
me way, they show detection of the real
in Fig.
cracks
cra
cr
cra
accks inside
i siide
in
de the
the specimen
th
spe
peci
cimen 3# at the modulation frequencies of
ci
0..1 H
0
z, 0.2
z,
0.2 Hz
0.
Hz and
a d 0.5
0.5 Hz.
0.1
Hz,
Th
T
he phase
pha
pha
h se
e angle
anglle contrast and the signal–noise
an
sig
The
ratio of defective
arre
a
ea
a (marked
(mar
(m
a ked in Fig. 16c) by Eq. (9) calculation are plotted in
area
Fig. 17a and b.
It was found that the phase angle contrast is increased with the
modulation frequency increasing, in this study, the modulation fre-
te
ht l:
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:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
As the SiC coating are formed
med on the surface
su
urrfa
u
f ce
e of
of C/C
C//C composite
com
ompo
posite
site
si
te
g CVR technique
e in
i the
th
he high
hiig
gh tempertempe
pe
errtest specimen 3# and 4# using
ds to generate real
rea
al cracks
cra
r ck
ks inner
in
nn
ner
er the
the
th
ature environment, which leads
asound wave was used
d to
to stimulate
s im
st
mulat
ullatte
specimen. The modulated ultrasound
g lock-in thermographic technique.
techn
hniq
ique
ue
ue.
the specimen 3# and 4# using
The signal–noise ratio (SNR)) of the phase angle image was defined to evaluate the performance of defect detection as following,
respectively:
SNR
SSN
N ¼
NR
Fig. 17. Phase angle contrast and signal–noise ration as function of the modulation frequencies: (a) phase angle contrast and (b) signal–noise ratio.
L. Junyan et al. / Composites: Part B 45 (2013) 138–147
147
Fig. 18. Phase angle image of specimen 4#: (a) ultrasound excitation at the modulation frequency of 0.1 Hz, (b) ultrasound excitation at the modulation frequency of 0.5 Hz
and (c) light excitation at the modulation frequency of 0.1 Hz.
quency of 0.5 Hz provides good phase angle contrast for the inner
crack defects from Fig. 17a, the signal–noise ratio of phase angle
image is decreased with the modulation frequency increasing, in
this investigation, the modulation frequency
q
y of 0.1 Hz provides
p
the highest signal–noise ratio
tio for the inner cracks defects from
fro
rom
rom
al–noise ratio is over 5.0
5..0 a
th
he
e range
r ng
ra
ge
Fig. 17b. However, the signal–noise
att the
5 Hz,
Hz,
z, in
in this
th
hiiss study,
sttud
st
ud
u
dy,
y,
of modulation frequencies from 0.1 Hz to 0.5
an
a
nd signal–noise
nd
sig
gn
na
a
al–
l n
l–
no
oiisse ratio
rat
atio
io
combining into the phase angle contrast and
tion frequency
cy of
cy
of 0.5
0..5 Hz
0
Hz is
is selected
selleccte
ted as
as
are considered, the modulation
ncy for the
he
e inner
iin
nne
nerr interfacial
in
ntte
errfa
faci
cia
ci
all crack
c ack decr
optimal modulation frequency
ound lock-in
lockk--in
k
i thermographic
th
he
errmo
mogrrap
aphi
h c technique.
fects detection using ultrasound
speci
cciimen 4#
4# by
by ULIT
ULIT are presented
pres
pr
esen
sen
ented
The phase angle images of specimen
hase angle
ang
gle image
e of
of specimen
specimen
n 4#
4# using
ussiing
ng
in Fig. 18a and b, and the phase
mps is
is shown
sh
hown
ow in
ow
in Fig. 18c.
lock-in thermography by lamps
e crack
cra
ra
ack
ck defects
de
d
efe
efe
fectts are
are observed from
m the
the
It can be seen that more
ultras
assou
a
und
d lock-in
loccck
lo
k-in thermography,, and
an
a
nd
phase angle image using ultrasound
dete
tecttab
te
blle
e from
fro
om the phase angle
e image
ima
mag
ge
e
the crack defects are hardly detectable
using lamps stimulation.
5. Conclusion
Acknowledgments
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ht l:
tp +8
:/ 6
/w 41
w 18
w 3
.il 72
gw 6
el 985
ls
.c
om
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Two active infrared thermographic
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com
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ind
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the temtemte
tem
to model the experimental test. The
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agr
g ee
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me
ent
n with
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th experimental
e pe
ex
p rimental
perature contrast of FEA is in good agreement
6.0
0 mm
mm defect
d fect
de
fe
ect
ct that
tha
th
att is by
measurement. The size of diameter 6.0
3.0
.0 mm
m defect
defect
de
defe
ffe
ec that
th
ha
att is
is by
by
3.0 mm deep and the size of diameter 3.0
temperatu
ure
re contrast
co
onttra
rast
ast
st image
ima
im
imag
ag
ge by
by
2.0 mm deep are detectable using temperature
phy with pulse heatt time
tim
im
me of
of 0.003
0.0
00
03
3 s.
s.
pulse transient thermography
tha
hat a
re by
The size of diameter 6.0 mm and 3.0 mm defects that
are
e using lock-in thermography at the
3.0 mm deep are detectable
modulation frequency of 0.05 Hz. The locations of defects are obtained by differential computation of normalized temperature contrast and normalized phase angle contrast. Ultrasound lock-in
thermography is available to detect cracks inside C/C composite,
and it compensates the disadvantage of lamps excitation for real
cracks detection using lock-in thermography.
the Fundamental Research Funds for the Central Universities under
Contract no. HIT.NSRIF.2009025 and the 111 Project (B07018).
te
This work was supported by the Chinese National Natural Science Foundation under Contract nos. 51074208 and 51173034,