Youssef 2009
Youssef 2009
Youssef 2009
Plastics
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What is This?
INTRODUCTION
in the majority of resin composites [1]; they are also used in rubber
composites [2]. Mixing the polar and hydrophilic fibers with nonpolar
hydrophobic matrix can result in difficulties associated with the
dispersion of the fibers in the polymeric matrix. The major factors
that govern the properties of short fiber composites are fiber dispersion,
fiber length, fiber orientation, and fiber–matrix adhesion [3]. Coupling
agents or compatibilizing agents are commonly employed to overcome
these problems [4]. These chemical reagents convert the hydrophilic
surface of cellulosic fiber to a hydrophobic one; as a result the fiber–
fiber hydrogen bonding is reduced, the dispersion of the fibers in the
matrix is enhanced and the adhesion is improved via the mechanism
such as entanglement, mechanical interlocking and formation of
physical or chemical bonds between treated fibers and the polymer
matrix [5]. Stael et al. [6] analyzed the composites formed by sugar
cane bagasse and thermoplastic polymer such as polystyrene, poly-
ethylene, and ethylene-co-vinyl acetate by NMR technique.
NMR responses showed that in EVA composite, bagasse can act as
reinforcement whereas in PS and PE composites bagasse acts as filler.
There are several reports on chemical modification of natural fibers,
these methods include bleaching [7] of fibers, alkaline and silane
treatment [8–10], acetylation [11] and cynaoethylation [9,10], reaction
treatment/coating with polymers [8,11], treatment with alkyl isocy-
nate [12,13], grafting polymerization of vinyl monomers [9,10].
The choice of chemical structure and the concentration of coupling
agents play an important role in achieving the optimum mechanical
properties of the composites [14].
Based on the fact that when thermoplastics are subjected to ionizing
radiation undergo structural changes accompanied by molecular cross-
linking, grafting, and chain scission reaction [15,16]. Jacobo et al. [17]
studied the effect of gamma irradiation (1–7 Mrads) on PP-HDPE-wood
fibers. It was found that the improvements in tensile strength were
insignificant.
From the proceeding literature, the effect of ionizing radiation
on bagasse fiber–thermoplastic composite properties has not been
extensively studied. Because electron beam (EB) irradiation has an
advantage over gamma irradiation, due to the latter being time
consuming and having an increased probability of severe oxidation
degradation of the composite, in this study EB irradiation is employed to
LDPE and HDPE prior to mixing with bagasse fibers. The effect of
bagasse fiber/thermoplastic ratio and irradiation dose on the properties
of the composites is investigated. Also, a mechanism of interaction
between composite components is suggested.
EXPERIMENTAL
Materials
NATURAL FIBERS
PLASTIC WASTE
ADDITIVES
in mixing for another 5 min. The sample was admixed for another 5 min
at high speed (50 rpm) to ensure that homogeneous mixing was
achieved. The sample was removed from the mixer and crushed to
small pieces. The crushed samples were pressed in a mold of dimensions
16 16 0.8 cm3, using an electric hot press type Carver-M-154. Hot
pressing was performed at the same processing temperature for each
plastic type, 5 min preheating and 10 min at 20,000 PSI and the sample
cooled at the same pressure for 5 min. The sample removed from the
mold and prepared for mechanical and physical testing.
Phsicomechanical Properties
STATIC BENDING
MOE ¼ P1 L3 =4 b d3 y ð2Þ
where,
b ¼ width of specimen in cm, d ¼ thickness of specimen in cm,
L ¼ length of span in cm, P ¼ maximum load (kg/cm2), P1 ¼ load at
proportional limit (kg/cm2), and y ¼ center of deflection at proportional
limit load in cm.
A
a¼ ð3Þ
b:h
where,
a ¼ the impact toughness in J/cm2, A ¼ absorbed impact energy in Joule,
b ¼ width of the sample in its center in cm, and h ¼ height of the sample
in its center in cm.
WATER ABSORPTION
MODULUS OF RUPTURE
25
LDPE
HDPE
20
Modulus of rupture (MPa)
15
10
5
10 20 30 40 50 60 70 80 90
Fiber ratio (wt.%)
MODULUS OF ELASTICITY
LDPE
HDPE
Modulus of elastcity (GPa)
0
10 20 30 40 50 60 70 80 90
Fiber ratio (wt.%)
IMPACT TOUGHNESS
2.0
1.8 LDPE
HDPE
1.6
Impact strength (J cm−2)
1.4
1.2
1.0
0.8
0.6
0.4
0.2
10 20 30 40 50 60 70 80 90
Fiber ratio (wt.%)
FIGURE 3. Impact strength of bagasse fibers-thermoplastic composites.
WATER ABSORPTION
Figure 4 illustrates the relation between increasing fiber ratio and the
percentage of WA of the composite samples. It is noticed that as the fiber
loading increase, the WA increase gradually; the increase become more
pronounced beyond 50 and 60% fiber loading for HDPE and LDPE,
respectively in which an abrupt increase in WA was observed. Also, it was
observed that WA% values for HDPE were higher than LDPE. This could
be due to that higher amorphous phase percentages (LDPE) can relatively
wets fibers compared to that posses higher crystallinity (HDPE). The
obtained data also reveals that the pronounced increase in percent of WA
occurs at a critical fiber concentration depending on the thermoplastic
used, beyond this concentration, the rate of WA increased remarkably.
This phenomenon can be elucidated as follows; below the critical
concentration, the thermoplastic represent the continuous phase
whereas bagasse fiber is the dispersion phase, therefore, the rate of
increasing WA was relatively small. The low percentage of WA is due to
that, bagasse fiber domains are completely encapsulated by thermo-
plastic phase. Hence, the chance of water penetration and as a result WA
by bagasse fibers was low. Beyond the critical concentration of bagasse
fibers, probably between 50% and 60% there are two co-continuous
phases are present at the same time. Beyond 60%, fibers represent the
continuous phase and the thermoplastic becomes the dispersed phase,
18
LDPE
16 HDPE
14
Water absorption (%)
12
10
4
10 20 30 40 50 60 70 80 90
Fiber ratio (wt.%)
FIGURE 4. Water absorption of bagasse fibers-thermoplastic composites.
30
25
20
15
10
5
0 10 20 30 40 50 60 70
Irradiation dose (kGy)
6
LDPE
HDPE
5
Modulus of elasticity (GPa)
1
0 10 20 30 40 50 60 70
Irradiation dose (kGy)
2.2
LDPE
2.0 HDPE
1.6
1.4
1.2
1.0
0 10 20 30 40 50 60 70
Irradiation dose (kGy)
FIGURE 7. Effect of electron beam irradiation on the impact strength of thermoplastics-
bagasse fiber composite.
LDPE
6.8 HDPE
6.4
6.2
6.0
0 10 20 30 40 50 60 70
Irradiation dose (kGy)
FIGURE 8. Effect of Electron beam irradiation dose on water absorption of bagasse fiber-
thermoplastic composites.
Irradiation
C C C C C* H C + H*
H2 H2 H2 H2 H2
O O*
C C* H C + O2 C C CH2
H2 H2 H2 H
O O* O
Heat
C C CH2 C C + O* H
H2 H H2 H2
Or
O O*
O
Heat +
C C CH2 C O* C
H2 H H2 H2
H
(RO*)
(a)
(b)
(a)
(b)
CONCLUSION
REFERENCES
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