Conductivity Studies of PMMA/Al 2 O 3 Composite

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Conductivity Studies of PMMA/Al 2 O 3 Composite S.Devikala*, P. Kamaraj and M. Arthanreeswari. Department of chemistry, SRM University, Kattankulathur, Tamil Nadu, India *Corresponding author s mail id: sdevikala@gmail.com Abstract Poly methyl methacrylate (PMMA) / Al 2 O 3 composites were prepared by sol gel method. The structural, micro structural and the dielectric properties of the composites were studied using X- ray diffraction( XRD), Scanning Electron Microscopy (SEM) and Hioki 3522-50 LCR Meter respectively. The electrical conductivity of composites has been investigated at different temperatures at frequency ranging from 50 Hz to 1MHZ. The dielectric loss, dielectric constant and conductivity were changed with change in the concentration of Al 2 O 3 and frequency of applied field. The electrical conductivities of the composites were found to increase with increasing temperature. Keywords- PMMA, Al2O3, electrical conductivity, polymer composite I. Introduction Composites can be defined as materials that consist of two or more chemically and physically different phases separated by a distinct interface. Composites, the wonder materials are becoming an essential part of todays materials due to the advantages such as low weight, corrosion resistance, high fatigue strength, and faster assembly. They are extensively used as materials in making aircraft structures, electronic packaging to medical equipment, and space vehicle to home building. Composite materials having long-term durability for continuous purposes are desirable and cost-effective. There is much interest in the development of inexpensive composite polymers with an appropriate weight, appropriate electric conductivity and/or appropriate impact value for use with practical articles Itoh et al (2006a), Itoh et al (2006b), Kanda et al (2009). Polymer composites have steadily gained growing importance during the past decade. A vigorous development of polymer composite and extensive utilization of polymer materials in technology have led to the polymer composites Wenderlinch (1973). The importance of polymers is mainly because polymers are still regarded as a cheap alternative material that is manufactured easily. The intensive use of polymer in broad use has led to the development of materials for specific applications namely composites Kryezewski (1975). Ceramic materials are typically brittle, possess low dielectric strength and in many cases are difficult to be processed requiring high temperature. On the other hand, polymers are flexible, can be easily processed at low temperatures and exhibit high dielectric break down field Mead (1961).A good amount of work has been reported on the conduction mechanism in polymeric materials. The electrical conduction in polymer film has much importance due to the discovery of the memory phenomenon and has wide applications now-a-days in thin film devices Chakraborty et al (1991). The electrical conduction in iodine doped polystyrene (PS) and poly(methyl methacrylate) (PMMA) has already been reported Sangawar et al (1995). Belsare et al (1998) measured the electrical conductivity of iodine doped polyblend films of polystyrene (PS) and poly(methyl methacrylate) (PMMA). Electrical conduction in semiconducting PVC PMMA thin film has been reported Deshmuk et al (2005). A. Chemicals and reagents II. EXPERIMENTAL The monomer MMA, Al 2 O 3, benzoyl peroxide, chloroform and petroleum ether were obtained from Alfa Aesar, India and used as such. B. Preparation of PMMA The purified monomer (MMA) (10ml) was taken in a polymeriz ation tube and 50mg of benzoyl peroxide which acts as a catalyst was added to accelerate polymerization, in the polymerization reaction. The polymerization tube was then kept in a water bath at 60-70 o C with periodical shaking. A hard viscous polymer was obtained after 90 minutes of heat treatment. The polymerized mass was dissolved in chloroform and then transferred into a beaker. The viscous polymer solution was precipitated by the addition of petroleum ether. The precipitated polymer was then filtered and oven dried at 60 o C. The polymer formed was found to be syndiotactic devikala et al (2011). C. Preparation of PMAl composites A definite quantity of PMMA was dissolved in chloroform followed by the addition of a known quantity of Al 2 O 3 and then it was made into a paste in an agate mortar then it was subjected to heat at 80 C for 1 hour in a Muffle furnace and made into a powder. PMAl composites were prepared in the following

proportions of PMMA and Al 2 O 3 : PMAl 1 9:1, PMAl 2 8:2, PMAl 3-7:3, PMAl 4-6:4,, PMAl 5 5:5 and PMAl 6 4:6. D. PXRD In order to understand the properties of composite material, it is essential to know about the details of its structure. The X-ray diffraction pattern (XRD) technique was used for characterization. The PXR D of PMMA, Al 2 O 3 and PMAl composites were recorded using Philips X PERT PRO diffractometer with Cu Kα (λ= 1.54060 Å) incident radiation. The XRD peaks were recorded in the 2θ range of 20 80. E. SEM The Scanning electron microscopy produces detailed photographs that provide important information about the surface structure. The morphology of PMMA, Al 2 O 3 and PMAl composites are recorded using Philips XL30. The samples were gold plated before SEM observation. F. Dielectric properties and conductivity measurement The electrical conductivity of composites were measured using Hioki 3522-50 LCR Meter. Testing temperature ranged from 40 to 60 C at frequency ranging from 50 Hz to 1MHZ. III. RESULTS AND DISCUSSION A. PXRD Pure PMMA showed a predominant and broad peak with a maximum at 2θ 13.89 along with broad but low-intensity peaks at 30 and 34. These broad peaks indicated the amorphous nature of the polymer (Fig.1). XRD of pure Al 2 O 3 is shown in the figure 20. Peaks at 37.88(110), 42.41 (113) and 67.09 (214) correspond to the diffraction patterns of Al 2 O 3 respectively. After the formation of the composite PMAl, the peaks were suppressed and a broad peaks appeaedr at 14 and 15 with a maximum at 15.04. This indicate an increase in the amorphous nature of composites. Thus the addition of Al 2 O 3 to PMMA may induce a significant increase in the amorphicity of composite materials. Fig. 1. XRD of PMMA Fig. 2. XRD of Al 2 O 3

Fig. 3. XRD of PMAl 6 B. SEM The SEM images of PMMA, Al 2 O 3 and the composite, PMAl 6 were shown in the figures 4,5 and 6 respectively. The composite possess smooth surface when compared to PMMA. The rough fractured surface of PMMA was changed due to the addition of Al 2 O 3. Fig. 4. SEM image of PMMA Fig. 5. SEM image of Al 2 O 3 The micrograph of pure PMMA shows a homogenous phase. SEM showed how the PMMA microspheres are inserted in the fine-grained solid-organic matrix. However, the PMMA contraction was found favourable, since this non-rigid behavior avoided the formation of cracks due to the absence of tensile stresses in the matrix. No density gradients of templates were observed in the cross sections analysed by sem, showing in all cases a homogenous microstructure. The inorganic moieties were well dispersed in the PMMA matrices. From the above observations it can be concluded that in our composite systems there was a good compatibility between the organic and inorganic components and the micro metred sized inorganic particles are well dispersed in the PMMA matrix. Fig. 6. SEM image of PMAl6

B. AC conductivity of PMMA/ Al 2 O 3 composites (IJIRSE) International Journal of Innovative Research in Science & Engineering The measured conductance G, from 50 Hz to 5000000Hz used to calculate ac conductivity, σ(ac) using the following expression: σ(ac) = G d/a where d is the thickness of the sample and A is the cross sectional area of the electrode. The AC conductivity of PMAl composites at different temperatures were shown in Table 1. Polymer materials in pure state are electrical insulators. However they are filled with specific additives, as metallic powders metallic fibers, ionic conductive polymers, etc. The conductivity of pure PMMA was found to be 5X10-18 S/cm. El-Bashir et al (2010). The electrical conductivity of the composite increased with the Al 2 O 3 content. The electrical conductivity of the composites exhibited a pronounced transition with the increase of Al 2 O 3 content, from an insulator to nearly a semiconductor. The increase of ac conductivity can be related to the electronic polarization as well as to the hopping of charge carrier over a small barrier height. The Table 1 indicates that ac conductivity is increased with increasing alumina content, a result which supports the suggestion of hopping charge carrier conduction mechanism This transition can be satisfactorily explained and described by the formation of the conductive network in the composite Pan et al (2000). As the temperature increased, the charge carries are thermally activated and the free volume increases and more vacant sites are created for the motion of ions, which in turn enhanced the conductivity. Table 1. shows the variation of conductivity with Al 2 O 3 concentration for different temperatures. Conductivity (S/cm) System studied 313K 323K 333K PMAl 1 1.48X10-9 1.95X10-8 1.56X10-7 PMAl 2 2.75X10-9 2.37 X10 8 2.56X10-7 PMAl 3 3.01X10-9 3.89 X10-8 3.89 X10-7 PMAl 4 4.41X10-9 4.92 X10-8 4.90 X10-7 PMAl 5 5.95X10-9 5.96 X10-8 5.75 X10-7 PMAl 6 6.68X10-9 6.80 X10-8 6.71 X10-7 C. Dielectric properties The higher value of dielectric constant is due to higher grain size. The dielectric constant strongly depends on the grain size.the dielectric constant of materials was due to the electronic, ionic, dipolar and surface charge polarizations which depend on the frequencies. The larger value of dielectric constant at lower frequency may be due to space charge polarization arising at the grain boundary interfaces. Figures 7 and 8 showed the variation of dielectric loss and dielectric constant as functions of frequency. In both the plots, the dielectric loss and dielectric constant decreased with the increase of frequency, which was in good agreement with the reported value Fang et al (2006).

Fig. 7. Variation of dielectric loss with frequency at 333K for PMAl 6 Fig. 8. Variation of dielectric constant with frequency at 333K for PMAl 6 IV. CONCLUSION Poly methyl methacrylate (PMMA) / Al 2 O 3 composites were prepared by sol gel method. The polymer composites were characterized using PXRD and SEM. The electrical conductivity and dielectric properties of the polymer composites were measured. The A.C electrical conductivity of the composites increases by increasing the Al 2 O 3 concentrations and with increased temperature. As the temperature increasef the charge carries were thermally activated and the free volume increases and more vacant sites are created for the motion of ions, which in turn enhances the conductivity. The dielectric loss and dielectric constant decreased with the increase of frequency. This was due to the electronic, ionic, dipolar and surface charge polarizations which depend on the frequencies. The large value of dielectric constant at lower frequency may be due to space charge polarization arising at the grain boundary interfaces. V. REFERENCES 1. K. Itoh, M. Kanda, Y. Nishi, J. Japan Inst. Metals. 70 (2006) pp.940 944. 2. M. Kanda, K. Itoh, Y. Nishi, J. Japan Inst. Metals. 70 (2006) pp. 945 949. 3. M. Kanda, Y. Nishi, Mater. Trans. 50 (2009) pp. 177 181.

4. Wenderlinch B."Macromolecular Physics", Academic press, New York. (1973) 5. Kryezewski M. Polym. Sci. Polym. Symp. (USA) 50 (1975) 359. 6. Mead C A. J. Appl. Phys. USA 33 (1961) 646. 7. Chakraborty S C, Patil N B, Das S K and Basu S. Indian J.Pure & Appl. Phys. 29 (1991) 478 8. Sangawar V S. Study of dielectric and other properties of doped thin film polystyrene (PS) and poly(methyl methacrylate) (PMMA) thermoelectrets, Ph D Thesis, Amravati University,Amravati (1995) 9. Belsare N G and Deogaonkar V S. Indian J. Pure & Appl. Phys. 36 (1998) 280. 10. Deshmukh S H, Burghate D K, Deogaonkar V S and Deshmukh P T. Indian J. Phys. 79 (2005) 1263. 11. Devikala, S, Kamaraj. E Journal of chemistry 8(S1) (2011) pp.165-170. 12. S. M. El-Bashir and A. Hindi. Polymer-Plastics Technology and Engineering, 49 (2010) pp. 78-82. 13. Pan YX, Yu ZZ, Ou YC, Hu GH. J. Polym Sci Part B: Polym Phys 38 (2000) 1626-33. 14. X S Fang, C H Ye, T Xie, ZY Wong, J W Zhao and L D Zhang. Appl. Phys. l88 ( 2006) 013101-013103