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recyclability,
energy
use,
and
environmental
INTRODUCTI considerations.
5
ON
End-use
Lignocellulosic natural fibers
applications of
such as sisal, coir, jute, ramie,
natural
fiber
pineapple leaf, and kenaf have
composites for
the potential to be used as a
decking,
replacement for glass or other
tradi-tional
reinforcementflooring,
materials in composites. Theseoutdoor
fibers have many propertiesfacilities,
that make them an attractive window
alternative
to
traditionalframes, various
materials. They have highconstruction
specific properties such asmaterials, and
stiffness, impact resistance,bath-room
parts,
for
14
flexibility, and modulus.
example, and
Combining kenaf fibers (KF)their exposure
with other resources provides ato
the
strategy
for
producingatmosphere or
advanced compos-ite materials
contact
with
that take advantage of the
aqueous media
properties of both types of
has
resources.
It
allows
the
scientist to design materials
based
on
end-use
requirements
within
a Corresponden
framework of cost, availability,ce to: Z. A. M.
Key
words:
kenafpolypropylene composite;
water
absorption;
dimensional
stability;
maleated polypropylene
Ishak
(zarifin.ishak@g
mail. com).
Journal
ofmade
it
Applied Polymernecessary
to
Science,
Vol.evaluate their
120,
563572water
uptake
(2011) VC 2010characteristics.
Wiley
6
Water
Periodicals, Inc.
absorption is
one of the
most important
characteristics
of
KF-filled
polypropylene
(PP/KF)
composite
exposed
to
environmental
condi-tions,
which
determines
their end-use
applications.
Therefore, as a
limiting
parameter,
water
absorption has
to be taken into
account in the
design
of
PP/KF
composites for
final
applications.
Similar
to
water
absorption,
fiber
content
and processing
can
affect
thickness
swelling
and
the
dimensional
stability
of
PP/KF
composites,
which is of
great
importance in
outdoor
applications
such
as
decking
and
7
railing.
In addition,
lignocellulosic
fibers used for
rein-forcement
in
nonpolar
thermoplastics,
such as poly-
behavior
ofof compatibilnatural
fiberizers
in
ther-moplastic reducing
the
composites
amount
and
has
beenrate of water
studied by aabsorption has
number
ofbeen
well
researchers, documented.9
and
theExtensive
effectiveness
research has
been
carried
out
with
different kinds
of
coupling
agents
for
surface
modification of
natural
564
TABLE I
Designation and Composition of Materials
Designation
Materials
PP (wt %)
KF (wt %)
MAPP (wt %)
PP
PP/KF20
PP/KF30
PP/KF40
PP/KF30/M5
PP/KF40/M5
PP
PP kenaf fiber
PP kenaf fiber
PP kenaf fiber
PP kenaf fiber MAPP
PP kenaf fiber MAPP
100
80
70
60
65
55
20
30
40
30
40
5
5
Compounding and
molding
The KF, 35 mm in
length, was initially
dried in a vacuum oven
at 80C for 24 hr. PP,
KF, and MAPP were
extruded using a corotating
twin-screw
extruder
(Model
PSW30) according to
the compositions given
in
Table
I.
The
extrusion
zone
temperature
ranged
from 155C to 175C.
The extrudate was
then pellet-ized with
the extruder pelletizer
(Model PSH10).
After compounding,
the tensile, flexural, and
impact samples were
prepared
by
melt
pressing
pel-lets
of
compounded
material
on a hot press machine
from Kao Tieh GoTech
Testing Machine Inc.
(Taipei, Taiwan). Before
molding,
all
compounded
pellets
were initially dried in a
vacuum oven at 80C for
24
hr
to
remove
moisture entrapped in
the materials. All PP/KF
composites
were
compression molded at
a temperature of 185C
and were preheated
without pressure for 10
min, compressed under
pressure of 10 MPa for
4 min, and cooled under
pressure for 4 min.
and
thick-ness
swelling. After vacuum
Fiber length distribution
drying at 80C for 24 hr
After compounding and molding, KF were taken to a constant weight to
from a small piece of sample using a chemical a precision of 0.001 g,
weight
of
diges-tion technique where xylene was used as the
before
the sol-vent. The fiber length distributions of 100 specimens
water immersion (W d)
fibers were determined with an image analyzer.
were measured with a
balance and thickness
Water absorption and dimensional stability test
was measured with a
thickness gauge (T0).
Water absorption tests were carried out according
The speci-mens were
to ASTM D-570 specifications. Flexural specimens
immersed in water at
were cut from the compression-molded plates and
room temperature for 7
used for the measurements of water absorption
Journal of Applied
weeks.
The weights of the
specimens
were
measured at regular
intervals
using
an
analytical balance. The
surfaces
of
these
specimens
were
thoroughly dried with
tissue papers, and they
were weighed immediately to determine the
weight
of
the
specimens (W w).
565
Flexural test
3366, at a crosshead
The percentage gain at any time t (Mt) as a result speed of 5 mm/min.
11
of water absorption was determined by eq. (1) : Five sam-ples of every
composition
were
Wwthe
Wdweight of the dry mawhere Wd and Ww denote
tested to obtain an
terial (the initial
weight of materials
before water
M %
100
average value.
Wd of materials after water
immersion) and t the weight
immersion, respectively. The specimens were
1
immersed until they were saturated.
The
diffusion
ThreeASTM Impa
M 4 Dt 2 (D) and the maximum water absorbed (M )
coefficient
m
point
D790- ct
t
Mm h p
can be obtained by considering the Ficks law
diffusion
bending
07. Fiveteste
model.
flexural
samples r at
tests
of everyroom
The equation of Ficks
law has been simplified by
12
were
composi-temp
Shen and Springer, to show that the initial absorpconducte
tion wereeratu
tion is given by:
d using
tested tore,
an
obtain acco
Instron
an
rding
model
average to
3366 at
value. AST
a
M
crosshea
Impact D611
d speed
0-08
test
of
5
(notc
mm/min
Charpy hed
and
a
impact sam
span
tests
ples)
length of
were
and
50 mm,
carried AST
accordin
out usingM
g
to
a Zwick
where Mt is the percentage of weight gain at any
time t, Mm is the maximum
absorbed at saturation, D is the mass diffusivity in
the composite, h is the thickness of specimen, and t
is the time of immersion.
The diffusion properties
where
k is laws
the initial
of the by
plotweight
of Mt versus
t1/2, Mm
by Ficks
wereslope
evaluated
gain measis the maximum weight gain, and h is the
urements of predried specimen immersed in water
thickness
of composite.
by considering
the slope
The thickness
swelling
weight
gain curve
versus (TS) was calculated according to the eq. (4):
using the following equation. The coefficient of diffusion (D) is defined as the slope of the normalized
1/2
mass uptake against t and has the form:
p
where T0 and Tw are D
thethicknesses
(mm) of the sample
4M
before and after immersion, respectively.
80
Tensile test
D4812
-06
(unnot
ched
sampl
e).
Both
the
notche
d and
unnotc
hed
sampl
es
were
tested
under
impact
energy
(2)
of
7.5 joules.
TS %
Tw T0
100
T0
S
c
a
n
ni
n
g
el
e
ct
ro
n
m
ic
ro
s
c
o
p
y
I
m
p
a
Journal
of
ct e
fr d
a wi
ct th
ur a
e fie
s ld
ur fa e
c mi
e ss
s io
of n
s S
a ca
mn
pl ni
en
s g
w El
er ec
e tr
eo
x n
a mi
m cr
in os
c
o
p
e
m
o(4)
d
el
Z
ei
ss
S
u
pr
a
3
5
V
P.
To
in
cr
e
a
s
e
th
e conductiv-ityshow
of the sampless the
and
reducefiber
the charginglengt
effects,
h
the
fracture
surface
was
coated
with of
adistrib
thin
layer
gold
using
aution
VG
MicrotechPolaron
of KF
Sputter
Coater
before
thebefor
scanning
electron
microscopy
e and
(SEM)
examination.
after
comp
RE oundi
SU ng. It
LTS can
AN be
D seen
DIS that
CU the
SSI lengt
ON h of
Fiber length the
fibers
distribution
was
Figure
1short
app
e
n
e
d
t
o
a
n
a
v
e
r
a
g
e