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Industrial Engineering Letters www.iiste.org
ISSN 2224-6096 (Paper) ISSN 2225-0581 (online)
Vol.3, No.7, 2013
60
Preparation and Study Optical Properties of (PVA-PVP-CrCl2)
Composites
Raya Ali Abed, Majeed Ali Habeeb
Babylon University, College of Education for pure science, Department of Physics, Iraq
E-mail:rayaali_88@yahoo.com
E-mail:majeed_ali74@yahoo.com
Abstract
In present research, the effect of addition chromium chloride (CrCl2) on the optical properties of (PVA-PVP)
composite has been studied, samples have been prepared by adding (CrCl2) to poly vinyl alcohol and poly vinyl
pyrrolidone with different weight percentages, the absorbance spectra was recorded in the wavelength range
(200-1100) nm. The absorption coefficient, optical energy gap of the indirect transition, extinction coefficient,
refractive index and (real, imaginary) dielectric constant have been determined.
Keywords: Optical properties, (PVA-PVP) composites, chromium chloride.
Introduction
The new composites materials have become the foundation to change and develop engineering designs for
many commodities and industrial products, the most important of these automotive industry, aircraft, ships, and
construction materials [1]. Polyvinyl alcohol has excellent film forming, emulsifying, and adhesive properties. It
is also resistant to oil, grease and solvent. PVA is odorless and nontoxic, as well as has high oxygen and aroma
barrier properties [2], its molecular formula is (C2H4O)x, and its density is between 1.19 and 1.31 g/cm3
[3]. PVP
is a white, hygroscopic powder with a weak characteristic order. In contrast to most polymers, it is readily
soluble in water and a large number of organic solvents, such as alcohols, amines, acids, chlorinated
hydrocarbons, amides, and lactams [4]. Many polymers in everyday use contain fillers and coloring agents that
render them opaque. The optical properties of the base polymer are thus obscured. On the other hand the clarity
of optical transmission of many polymers and the fact that they are almost colorless, coupled with their low
density and excellent mechanical properties, are the reasons for their use to replace glass in many applications
[5].
Experimental work
Three films from (PVA-PVP-CrCl2) composites have been prepared by adding chromium chloride to (PVA-
PVP) with different weight percentages of salt concentration (3,6,9)wt.%. Preparation of films have been done
by using casting method. The absorbance spectra recorded in the wave length (200-1100) nm by using UV
spectrophotometer (UV-1800), the absorption coefficient(α) was calculated from the following equation: [6]
α= 2.303 A/d (1)
Where A is absorption and d is the sample thickness
The optical energy gap has been calculated by using this equation: [7]
αhf= B (hf –Eg)r
(2)
Where hf is the energy of photon, B is proportionality constant and Eg is optical energy gap.
The extinction coefficient (k) is directly proportional to the absorption coefficient (α): [8]
k=αλ/4π (3)
Where λ is the wavelength of light.
The refractive index has been calculated by using this equation: [9]
n= [4R/(R-1)2
- (R+1/R-1)]1/2
(4)
The real and imaginary part of dielectric constants have been determined from this equation:[10]
ε1
=n2
-k2
(5)
ε2=2nk (6)
Results and Discussion
The absorbance of (PVA-PVP-CrCl2) composite with varies concentration over wavelength (200-1100) nm
was recorded at room temperature. Figure (1) display the variation of optical absorbance with wave length for
(PVA-PVP-CrCl2) composite. The intensity of the peak increasing and no shift in the peak position. The
absorbance increases with increasing of weight percentages of the chloride, this is due to absorb the incident
light by free electrons [11].
Industrial Engineering Letters www.iiste.org
ISSN 2224-6096 (Paper) ISSN 2225-0581 (online)
Vol.3, No.7, 2013
61
Figure (1): Variation between absorbance with wavelength for (PVA-PVP-CrCl2) composite.
Figure (2) shows the relation between the absorption coefficient and photon energy of the (PVA-PVP-CrCl2)
composite. From this figure notice that the absorption coefficient dependent on the photon energy, where the
absorption is little at low energy this is means that the possibility of electron transition is little because the
energy of the incident photon is notice sufficient to move the electron from the valance band to the conduction
band. At high energies the absorption coefficient assists in figuring out the nature of electron transition when the
values of the absorption coefficient is high (α >104
) cm-1
it is expected that direct transition of electron occur on
the other band when the values of absorption coefficient is low (α <104
) cm-1
it is expected that indirect
transition of electron occur [12].
Figure(2): Relationship between absorption coefficient and photon energy for (PVA-PVP-CrCl2)
composite.
The variation between ((αhf) 1/2
(cm-1
.eV)1/2
) and photon energy of (PVA-PVP-CrCl2) composite shown in
figures (3). It is appear from this figure the values of optical energy gap decrease by increasing weight
percentages from (CrCl2) this is attributed to the increase of disorder in the material, that means allowing
excitation secondary levels inside the energy gap and increase the width of these levels with the increasing of
(CrCl2) concentration which leads to decrease the width gap. Figure (4) show the relationship between ((αhf)1/3
(cm-1
.eV)1/3
) and photon energy of composites, we can see from this figure the values of energy gap for
forbidden indirect transition decrease by increasing weight percentages of chlorides, as well as these values of
forbidden indirect transition are less than the values of allowed indirect transition [13]. The values of optical
energy gap for indirect transition (allowed, forbidden) for all samples shown in table (1).
0
10
20
30
40
50
60
70
80
90
100
200 300 400 500 600 700 800
Absorbance%
Wavelength(nm)
pure
3 wt.%
6 wt.%
9 wt.%
0
200
400
600
800
1000
1200
1400
0 1 2 3 4 5 6 7
Photon energy(eV)
pure
3 wt.%
6 wt.%
9 wt.%
α(cm)-1
Industrial Engineering Letters www.iiste.org
ISSN 2224-6096 (Paper) ISSN 2225-0581 (online)
Vol.3, No.7, 2013
62
Figure (3): Relationship between (αhf)1/2
(cm-1
.eV)1/2
and photon energy for (PVA-PVP-CrCl2) composite.
Figure (4): Relationship between (αhf)1/3
(cm-1
.eV)1/3
and photon energy for (PVA-PVP-CrCl2) composite.
Table (1): Values of the optical energy gap of indirect transition for all samples.
Optical energy gap for indirect transition
Samples
Allowed Forbidden
PVA-PVP-CrCl2 PVA-PVP-CrCl2
pure 4.85 4.6
3wt.% 4.39 3.95
6wt.% 4.3 3.9
9wt.% 4.2 3.8
Figure (5) show the relationship between refractive index and photon energy for (PVA-PVP-CrCl2)
composites. It is obvious from this figure the refractive index increase with increasing of chloride concentration
because of increasing in density composites. In ultraviolet region we note that high values of the refractive index
because of the little transmittance in this region, but in the visible region note that low values because of the high
transmittance in this region [14].
0
10
20
30
40
50
60
70
80
90
0 1 2 3 4 5 6 7
Photon energy(eV)
pure
3 wt.%
6 wt.%
9 wt.%
(αhf)1/2(cm-1.eV)1/2
0
5
10
15
20
25
0 1 2 3 4 5 6 7
Photon energy(eV)
pure
3 wt.%
6 wt.%
9 wt.%
(αhf)1/3(cm-1.eV)1/3
.
Industrial Engineering Letters www.iiste.org
ISSN 2224-6096 (Paper) ISSN 2225-0581 (online)
Vol.3, No.7, 2013
63
Figure (5): Relationship between refractive index and photon energy for (PVA-PVP-CrCl2) composite.
The variation of the extinction coefficient for (PVA-PVP-CrCl2) composite as a function of wavelength
shown in figure (6). This figure show that extinction coefficient (k) has low values at (UV-region) and with the
little concentration, as well as it is increased with increasing of additive concentrations of chlorides because of
increasing in absorption coefficient, but at visible region we note that the extinction coefficient is very low
because of the low absorption at this region[15].
Figure (6): Extinction coefficient for (PVA-PVP-CrCl2) composite with photon energy.
The dielectric constant for two parts (real and imaginary) have been calculated from equations (5) and (6).
Figure (7) show the variation between real part of dielectric constant (ε1) with photon energy. It is concluded that
the variation of (ε1) mainly dependence on (n2
) because of small values of (k2
), while (ε2) mainly dependence on
the (k) values which are related the variation of absorption coefficient, as shown in figure (8).
1
1.2
1.4
1.6
1.8
2
0 1 2 3 4 5 6 7
n
Photon energy(eV)
pure
3 wt.%
6 wt.%
9 wt.%
0.E+00
5.E-04
1.E-03
2.E-03
2.E-03
3.E-03
3.E-03
4.E-03
0 1 2 3 4 5 6 7
k
Photon energy(eV)
pure
3 wt.%
6 wt.%
9 wt.%
Industrial Engineering Letters www.iiste.org
ISSN 2224-6096 (Paper) ISSN 2225-0581 (online)
Vol.3, No.7, 2013
64
Figure (7): Relation between real part of dielectric constant (ε1) with photon energy for (PVA-PVP-CrCl2)
composite.
Figure (8): Relation between imaginary part of dielectric constant (ε2) with photon energy for (PVA-PVP-
CrCl2) composite.
Conclusions
1- The absorption coefficient for all composites has more increased in (UV-region) and less increased in a
visible region, generally the absorption coefficient increased with increasing of chloride concentration.
2- The energy gap for indirect transition (allowed, forbidden) decreased with increasing of chloride
concentration.
3- Extinction coefficient has low values, generally it is increased with increasing of concentration for all samples.
4- Refractive index and dielectric constant (real, imaginary) increased with increasing of concentration for all
samples.
References
[1] R.B. Seymour, "Polymer composites", 1st
ed., Utrecht, The Nether Lands, 1990.
[2] V. Sedlarik, N. Saha, I. Kuritka, and P. Saha. Environmentally friendly biocomposites based on
waste of the dairy industry and poly(vinyl alcohol)", Journal of Applied Polymer Science,
Vol.106, No.3, pp.1869-1879, 2007.
[3] J. Fromageau, E. Brusseau, D. Vray, G. Gimenez, and P. Delachartre,"Characterization of PVA
cryogel for intravascu-lar ultrasound elasticity imaging", IEEE Transactions on Ultrasonic,
Vol.50, No.10, pp.1318-1324, 2003.
[4] A.H. Nomani, "Study the effect of gamma rays on some physical properties of the polymer
hydroxyethyl", cellulose and cellulose instance, M.Sc Thesis, University of Babylon-Faculty of
Science, 2000.
1
1.5
2
2.5
3
3.5
4
4.5
5
0 1 2 3 4 5 6 7
Photon energy(eV)
pure
3 wt.%
6 wt.%
9 wt.%
ε1
0
0.002
0.004
0.006
0.008
0.01
0.012
0 1 2 3 4 5 6 7
Photon energy(eV)
pure
3 wt.%
6 wt.%
9 wt.%
ε2
Industrial Engineering Letters www.iiste.org
ISSN 2224-6096 (Paper) ISSN 2225-0581 (online)
Vol.3, No.7, 2013
65
[5] I. David, "Introduction to physical polymer", new Cambridge University press, 2002.
[6] C. Mwolfe, N. Holouyak and G.B. Stillman, "Physical properties of Semiconductor", prentice
Hall, New York, 1989.
[7] G. Sami Salman, "optical and structural properties of SnO2 membranes Tinged by fluorosis and
gamma-ray irradiated", Master, Faculty of Sciences, University of Baghdad, 2005.
[8] R Tintu, K. Saurav, K. Sulakshna, Vpn. Nampoori, Pradha krishnan and Sheenuthomas,
"Ge28Se60Sb12 /PVA composite films for photonic application", Journal of Non-Oxide Glasses,
Vol. 2, No 4, pp.167-174, 2010.
[9] B. H. F. AL-Khayat and F. A. Awni, J. Am. Ceram. Soc. Bull., 64(4), pp598-601, 1985.
[10] M. Revanasiddappa, S.C. Raghavendra, S. Khasim and T.K. Vishnuvardhan, J. Bull. Korean
chem., Soc. Vol. 28 , No.7, pp.1104-1108, 2007.
[11] P.U. Asogwa, "Band gap shift and optical characterization of Capped PbO thin films: Effect of thermal
annealing", Chalcogenide Letters, Vol.8, No.3, pp.163-170, 2011.
[12] G. Pinto and Abdel-Karim Maaroufi, "Critical filler concentration for electro conductive
polymer composites", Society of Plastics Engineers (SPE), 10.1002/ spepro.003521, 2011.
[13] M. Dahshan, "Introduction to material science and Engineering", 2nd
ed., 2002.
[14] M.K. Mahsan1, C.K. Sheng1, M.I. Isa1, E. Ghapur E. Ali and M.H. Razali, "Structural and
Physical Properties of PVA/ TiO2 Composite", Malaysia Polymer International Conference,
pp.486-495, 2009.
[15] K. Bula1, T. Jesionowski and S. Borysiak, Proceedings of the Conference of Multiphase
Polymers and Polymer Composites: From Nan scale to Macro Composites, Paris-Est, Creteil
University, France, 2011.
This academic article was published by The International Institute for Science,
Technology and Education (IISTE). The IISTE is a pioneer in the Open Access
Publishing service based in the U.S. and Europe. The aim of the institute is
Accelerating Global Knowledge Sharing.
More information about the publisher can be found in the IISTE’s homepage:
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Preparation and study optical properties of (pva pvp-cr cl2) composites

  • 1. Industrial Engineering Letters www.iiste.org ISSN 2224-6096 (Paper) ISSN 2225-0581 (online) Vol.3, No.7, 2013 60 Preparation and Study Optical Properties of (PVA-PVP-CrCl2) Composites Raya Ali Abed, Majeed Ali Habeeb Babylon University, College of Education for pure science, Department of Physics, Iraq E-mail:rayaali_88@yahoo.com E-mail:majeed_ali74@yahoo.com Abstract In present research, the effect of addition chromium chloride (CrCl2) on the optical properties of (PVA-PVP) composite has been studied, samples have been prepared by adding (CrCl2) to poly vinyl alcohol and poly vinyl pyrrolidone with different weight percentages, the absorbance spectra was recorded in the wavelength range (200-1100) nm. The absorption coefficient, optical energy gap of the indirect transition, extinction coefficient, refractive index and (real, imaginary) dielectric constant have been determined. Keywords: Optical properties, (PVA-PVP) composites, chromium chloride. Introduction The new composites materials have become the foundation to change and develop engineering designs for many commodities and industrial products, the most important of these automotive industry, aircraft, ships, and construction materials [1]. Polyvinyl alcohol has excellent film forming, emulsifying, and adhesive properties. It is also resistant to oil, grease and solvent. PVA is odorless and nontoxic, as well as has high oxygen and aroma barrier properties [2], its molecular formula is (C2H4O)x, and its density is between 1.19 and 1.31 g/cm3 [3]. PVP is a white, hygroscopic powder with a weak characteristic order. In contrast to most polymers, it is readily soluble in water and a large number of organic solvents, such as alcohols, amines, acids, chlorinated hydrocarbons, amides, and lactams [4]. Many polymers in everyday use contain fillers and coloring agents that render them opaque. The optical properties of the base polymer are thus obscured. On the other hand the clarity of optical transmission of many polymers and the fact that they are almost colorless, coupled with their low density and excellent mechanical properties, are the reasons for their use to replace glass in many applications [5]. Experimental work Three films from (PVA-PVP-CrCl2) composites have been prepared by adding chromium chloride to (PVA- PVP) with different weight percentages of salt concentration (3,6,9)wt.%. Preparation of films have been done by using casting method. The absorbance spectra recorded in the wave length (200-1100) nm by using UV spectrophotometer (UV-1800), the absorption coefficient(α) was calculated from the following equation: [6] α= 2.303 A/d (1) Where A is absorption and d is the sample thickness The optical energy gap has been calculated by using this equation: [7] αhf= B (hf –Eg)r (2) Where hf is the energy of photon, B is proportionality constant and Eg is optical energy gap. The extinction coefficient (k) is directly proportional to the absorption coefficient (α): [8] k=αλ/4π (3) Where λ is the wavelength of light. The refractive index has been calculated by using this equation: [9] n= [4R/(R-1)2 - (R+1/R-1)]1/2 (4) The real and imaginary part of dielectric constants have been determined from this equation:[10] ε1 =n2 -k2 (5) ε2=2nk (6) Results and Discussion The absorbance of (PVA-PVP-CrCl2) composite with varies concentration over wavelength (200-1100) nm was recorded at room temperature. Figure (1) display the variation of optical absorbance with wave length for (PVA-PVP-CrCl2) composite. The intensity of the peak increasing and no shift in the peak position. The absorbance increases with increasing of weight percentages of the chloride, this is due to absorb the incident light by free electrons [11].
  • 2. Industrial Engineering Letters www.iiste.org ISSN 2224-6096 (Paper) ISSN 2225-0581 (online) Vol.3, No.7, 2013 61 Figure (1): Variation between absorbance with wavelength for (PVA-PVP-CrCl2) composite. Figure (2) shows the relation between the absorption coefficient and photon energy of the (PVA-PVP-CrCl2) composite. From this figure notice that the absorption coefficient dependent on the photon energy, where the absorption is little at low energy this is means that the possibility of electron transition is little because the energy of the incident photon is notice sufficient to move the electron from the valance band to the conduction band. At high energies the absorption coefficient assists in figuring out the nature of electron transition when the values of the absorption coefficient is high (α >104 ) cm-1 it is expected that direct transition of electron occur on the other band when the values of absorption coefficient is low (α <104 ) cm-1 it is expected that indirect transition of electron occur [12]. Figure(2): Relationship between absorption coefficient and photon energy for (PVA-PVP-CrCl2) composite. The variation between ((αhf) 1/2 (cm-1 .eV)1/2 ) and photon energy of (PVA-PVP-CrCl2) composite shown in figures (3). It is appear from this figure the values of optical energy gap decrease by increasing weight percentages from (CrCl2) this is attributed to the increase of disorder in the material, that means allowing excitation secondary levels inside the energy gap and increase the width of these levels with the increasing of (CrCl2) concentration which leads to decrease the width gap. Figure (4) show the relationship between ((αhf)1/3 (cm-1 .eV)1/3 ) and photon energy of composites, we can see from this figure the values of energy gap for forbidden indirect transition decrease by increasing weight percentages of chlorides, as well as these values of forbidden indirect transition are less than the values of allowed indirect transition [13]. The values of optical energy gap for indirect transition (allowed, forbidden) for all samples shown in table (1). 0 10 20 30 40 50 60 70 80 90 100 200 300 400 500 600 700 800 Absorbance% Wavelength(nm) pure 3 wt.% 6 wt.% 9 wt.% 0 200 400 600 800 1000 1200 1400 0 1 2 3 4 5 6 7 Photon energy(eV) pure 3 wt.% 6 wt.% 9 wt.% α(cm)-1
  • 3. Industrial Engineering Letters www.iiste.org ISSN 2224-6096 (Paper) ISSN 2225-0581 (online) Vol.3, No.7, 2013 62 Figure (3): Relationship between (αhf)1/2 (cm-1 .eV)1/2 and photon energy for (PVA-PVP-CrCl2) composite. Figure (4): Relationship between (αhf)1/3 (cm-1 .eV)1/3 and photon energy for (PVA-PVP-CrCl2) composite. Table (1): Values of the optical energy gap of indirect transition for all samples. Optical energy gap for indirect transition Samples Allowed Forbidden PVA-PVP-CrCl2 PVA-PVP-CrCl2 pure 4.85 4.6 3wt.% 4.39 3.95 6wt.% 4.3 3.9 9wt.% 4.2 3.8 Figure (5) show the relationship between refractive index and photon energy for (PVA-PVP-CrCl2) composites. It is obvious from this figure the refractive index increase with increasing of chloride concentration because of increasing in density composites. In ultraviolet region we note that high values of the refractive index because of the little transmittance in this region, but in the visible region note that low values because of the high transmittance in this region [14]. 0 10 20 30 40 50 60 70 80 90 0 1 2 3 4 5 6 7 Photon energy(eV) pure 3 wt.% 6 wt.% 9 wt.% (αhf)1/2(cm-1.eV)1/2 0 5 10 15 20 25 0 1 2 3 4 5 6 7 Photon energy(eV) pure 3 wt.% 6 wt.% 9 wt.% (αhf)1/3(cm-1.eV)1/3 .
  • 4. Industrial Engineering Letters www.iiste.org ISSN 2224-6096 (Paper) ISSN 2225-0581 (online) Vol.3, No.7, 2013 63 Figure (5): Relationship between refractive index and photon energy for (PVA-PVP-CrCl2) composite. The variation of the extinction coefficient for (PVA-PVP-CrCl2) composite as a function of wavelength shown in figure (6). This figure show that extinction coefficient (k) has low values at (UV-region) and with the little concentration, as well as it is increased with increasing of additive concentrations of chlorides because of increasing in absorption coefficient, but at visible region we note that the extinction coefficient is very low because of the low absorption at this region[15]. Figure (6): Extinction coefficient for (PVA-PVP-CrCl2) composite with photon energy. The dielectric constant for two parts (real and imaginary) have been calculated from equations (5) and (6). Figure (7) show the variation between real part of dielectric constant (ε1) with photon energy. It is concluded that the variation of (ε1) mainly dependence on (n2 ) because of small values of (k2 ), while (ε2) mainly dependence on the (k) values which are related the variation of absorption coefficient, as shown in figure (8). 1 1.2 1.4 1.6 1.8 2 0 1 2 3 4 5 6 7 n Photon energy(eV) pure 3 wt.% 6 wt.% 9 wt.% 0.E+00 5.E-04 1.E-03 2.E-03 2.E-03 3.E-03 3.E-03 4.E-03 0 1 2 3 4 5 6 7 k Photon energy(eV) pure 3 wt.% 6 wt.% 9 wt.%
  • 5. Industrial Engineering Letters www.iiste.org ISSN 2224-6096 (Paper) ISSN 2225-0581 (online) Vol.3, No.7, 2013 64 Figure (7): Relation between real part of dielectric constant (ε1) with photon energy for (PVA-PVP-CrCl2) composite. Figure (8): Relation between imaginary part of dielectric constant (ε2) with photon energy for (PVA-PVP- CrCl2) composite. Conclusions 1- The absorption coefficient for all composites has more increased in (UV-region) and less increased in a visible region, generally the absorption coefficient increased with increasing of chloride concentration. 2- The energy gap for indirect transition (allowed, forbidden) decreased with increasing of chloride concentration. 3- Extinction coefficient has low values, generally it is increased with increasing of concentration for all samples. 4- Refractive index and dielectric constant (real, imaginary) increased with increasing of concentration for all samples. References [1] R.B. Seymour, "Polymer composites", 1st ed., Utrecht, The Nether Lands, 1990. [2] V. Sedlarik, N. Saha, I. Kuritka, and P. Saha. Environmentally friendly biocomposites based on waste of the dairy industry and poly(vinyl alcohol)", Journal of Applied Polymer Science, Vol.106, No.3, pp.1869-1879, 2007. [3] J. Fromageau, E. Brusseau, D. Vray, G. Gimenez, and P. Delachartre,"Characterization of PVA cryogel for intravascu-lar ultrasound elasticity imaging", IEEE Transactions on Ultrasonic, Vol.50, No.10, pp.1318-1324, 2003. [4] A.H. Nomani, "Study the effect of gamma rays on some physical properties of the polymer hydroxyethyl", cellulose and cellulose instance, M.Sc Thesis, University of Babylon-Faculty of Science, 2000. 1 1.5 2 2.5 3 3.5 4 4.5 5 0 1 2 3 4 5 6 7 Photon energy(eV) pure 3 wt.% 6 wt.% 9 wt.% ε1 0 0.002 0.004 0.006 0.008 0.01 0.012 0 1 2 3 4 5 6 7 Photon energy(eV) pure 3 wt.% 6 wt.% 9 wt.% ε2
  • 6. Industrial Engineering Letters www.iiste.org ISSN 2224-6096 (Paper) ISSN 2225-0581 (online) Vol.3, No.7, 2013 65 [5] I. David, "Introduction to physical polymer", new Cambridge University press, 2002. [6] C. Mwolfe, N. Holouyak and G.B. Stillman, "Physical properties of Semiconductor", prentice Hall, New York, 1989. [7] G. Sami Salman, "optical and structural properties of SnO2 membranes Tinged by fluorosis and gamma-ray irradiated", Master, Faculty of Sciences, University of Baghdad, 2005. [8] R Tintu, K. Saurav, K. Sulakshna, Vpn. Nampoori, Pradha krishnan and Sheenuthomas, "Ge28Se60Sb12 /PVA composite films for photonic application", Journal of Non-Oxide Glasses, Vol. 2, No 4, pp.167-174, 2010. [9] B. H. F. AL-Khayat and F. A. Awni, J. Am. Ceram. Soc. Bull., 64(4), pp598-601, 1985. [10] M. Revanasiddappa, S.C. Raghavendra, S. Khasim and T.K. Vishnuvardhan, J. Bull. Korean chem., Soc. Vol. 28 , No.7, pp.1104-1108, 2007. [11] P.U. Asogwa, "Band gap shift and optical characterization of Capped PbO thin films: Effect of thermal annealing", Chalcogenide Letters, Vol.8, No.3, pp.163-170, 2011. [12] G. Pinto and Abdel-Karim Maaroufi, "Critical filler concentration for electro conductive polymer composites", Society of Plastics Engineers (SPE), 10.1002/ spepro.003521, 2011. [13] M. Dahshan, "Introduction to material science and Engineering", 2nd ed., 2002. [14] M.K. Mahsan1, C.K. Sheng1, M.I. Isa1, E. Ghapur E. Ali and M.H. Razali, "Structural and Physical Properties of PVA/ TiO2 Composite", Malaysia Polymer International Conference, pp.486-495, 2009. [15] K. Bula1, T. Jesionowski and S. Borysiak, Proceedings of the Conference of Multiphase Polymers and Polymer Composites: From Nan scale to Macro Composites, Paris-Est, Creteil University, France, 2011.
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