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- Table of Contents
Journal of Nanomaterials
Volume 2012 (2012), Article ID 932059, 6 pages
Microstructure and Mechanical Properties of Heterogeneous Ceramic-Polymer Composite Using Interpenetrating Network
1School of Nano & Advanced Materials Engineering, Changwon National University, Changwon, Kyungnam 641-773, Republic of Korea
2High Temperature Materials Research Group, Korea Institute of Materials Science, Changwon, Gyeongnam 641-831, Republic of Korea
Received 5 March 2012; Accepted 22 March 2012
Academic Editor: Sevan P. Davtyan
Copyright © 2012 Eun-Hee Kim et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Prepolymer, which can be polymerized by a photo, has been infiltrated into a porous ceramic to improve the addition effect of polymer into the ceramic, as a function of the functionality of prepolymer. It induces the increase in the mechanical properties of the ceramic. The porous alumina (Al2O3) and the polyurethane acrylate (PUA) with a network structure by photo-polymerization were used as the matrix and infiltration materials, respectively. The porous Al2O3 matrix without the polymer shows lower values in fracture strength than the composites, since the stress is transmitted more quickly via propagation of cracks from intrinsic defects in the porous matrix. However, in the case of composites, the distribution of stress between heterophases results in the improved mechanical properties. In addition, the mechanical properties of composites, such as elastic modulus and fracture strength, are enhanced with increasing the functionality of prepolymer attributed to the crosslinking density of polymer.
Porous alumina (Al2O3) has been widely used as hot gas filtration, catalyst support, filtration for heavy metal ions in water, chromatography, and fine or microchannels for electrophoresis, owing to its excellent physical and chemical properties such as acid resistance and chemical stability [1, 2]. However, its use in practical applications has been impeded by its naturally low mechanical property, which has been a bottleneck in the scientific and technological point of view. Therefore, a ceramic-polymer composite has been introduced as a new class of construction and functional materials for industrial applications, which can combine the hardness and stiffness of ceramic and the rubber elasticity of polymer [3–7]. De Salazar et al. has studied the mechanical properties of composites fabricated with the cellular ceramic (SiC and SiO2·ZrO2) and the epoxy resin, as a function of cell size . Brandt et al. has researched the novel ceramic-polymer composites through polymer-encapsulated TiO2 nanoparticles . However, the composite with the TiO2 shows low mechanical properties, resulting from the no-sintering of composite due to the heat treatment at the relatively low temperature. In addition, various works related to the mechanical properties of ceramic-polymer composites affected by elasticity of polymer used as a reinforcement material have not been researched yet.
Therefore, in this work, to effectively increase the mechanical properties of porous ceramic, two key points have been considered in the fabrication of desirable composite. One is to use the prepolymer which has extremely lower viscosity than polymer. Polymer has generally a gel phase of high viscosity due to the long chain by join with a lot of monomers, deteriorating the dispersibility of polymer into matrix. Therefore, the prepolymer of a sol phase, which can be polymerized by a photo, has been infiltrated into the porous ceramic to maximize the addition effect of polymer into the ceramic matrix. This interpenetrating network (IPN) method increases the universal properties of the ceramic matrix by the homogeneous dispersion of prepolymer into the ceramic matrix. Namely, it is far preferable to incorporate the polymer into the ceramic matrix by covalent bonding between polymer chains than by simply mixing them by shear. The ultraviolet (UV) curing used in this work is one of well-known photopolymerization methods and has been employed at various industrial applications. Its advantages include energy savings, and it yields products with high durability and high scratch resistance. The other is to use polyurethane (PU) which easily changes the elastic modulus of polymer controlled by crosslinking density. PU is the most versatile polymer material, leading to its use in many different applications, for example, in building materials, sports goods, medical equipment, adhesives, and coatings [10–12]. Consequently, the prepolymer infiltrated in the porous matrix has been polymerized by free-radical photopolymerization as a function of the functionality of prepolymer, in efforts to increase the mechanical properties, such as elastic modulus and fracture strength. The microstructure and mechanical properties of the prepared PUA-Al2O3 composites have been observed and measured, respectively, using various analytical techniques.
2. Experimental Procedure
The polyurethane acrylate (PUA) oligomers were synthesized from polypropylene glycol (PPG Mn = 300, Sigma-Aldrich Korea, Yongin, Republic of Korea) and hexamethylene diisocyanate (HDI, Sigma-Aldrich Korea, Yongin, Republic of Korea) to form isocyanate-terminated prepolymer. PPGs were dried at 80°C with 0.1 mm Hg for several hours until no bubbling was observed. Extra pure grade of HDI was used without further purification. A molar excess of HDI was reacted with PPG for over 1 h at 80°C to obtain HDI-terminated prepolymer. Then, the reacted mixture was cooled down to 40°C, and hydroxyethyl methacrylate (HEMA, Sigma-Aldrich Korea, Yongin, Republic of Korea) was added to obtain HEMA-capped urethane oligomer . Completion of the reaction was confirmed by the disappearance of NCO peak at 2270 cm−1 in the Fourier transform infrared spectroscopy (FT-IR) analysis.
The polymer used in this work was prepared from a homogeneous prepolymer mixture consisting of the PUA oligomer, the reactive diluent, namely, N-vinylpyrrolidone (NVP, Sigma-Aldrich Korea, Yongin, Republic of Korea), and 2-hydroxy-2-methyl-1-phenyl propane-1-one (Darocur 1173, Ciba in Korea, Seoul, Republic of Korea) as a photoinitiator. The prepolymer compositions were fixed at 1/1 and 3/1 (oligomer/NVP) by weight ratio to investigate the effect of crosslinking density of polymer. The green body of ceramic matrix was prepared by an uniaxial pressing process with Al2O3 powder, and then the prepared green body was heat treated at 1000°C for 1 h. At room temperature, the mixed prepolymer was infiltrated into the Al2O3 matrix in a vacuum chamber for the homogeneous infiltration of prepolymer mixture into all pores of ceramic matrix. The prepolymer-infiltrated matrix was cured by UV light (1.5 mW/cm2, 365 nm) for 3 min. The synthetic scheme for the PUA-Al2O3 composite is given in Figure 1, and the basic formulations employed to prepare PUA film and PUA-Al2O3 composites are shown in Tables 1 and 2, respectively.
Dynamic mechanical properties of the polymer films were measured using DMTA (Rheometric Scientific MK) at a heating rate of 4°C/min and 10 Hz. The difference before and after the polymerization of PUA and the presence of PUA in Al2O3 matrix were analyzed using a Fourier transform infrared spectrometer (Nicolet, Thermo Fisher Scientific, MA, USA). The microstructure of composite was observed using a scanning electron microscope (SEM; JEOL Model JSM-5610, Tokyo, Japan). The porosity of composite was measured by mercury porosimeter (AutoPore Iv berries, Micromeritics GmbH, Rutherford, NJ, USA). The fracture strength and elastic modulus of PUA-Al2O3 composite were measured with a universal testing machine (UTM, Instron 5566, Instron Corp., Norwood, MA, USA) in the bending mode at a rate of 0.5 mm min−1. The hardness values of composites were measured using a Vickers indenter (HM-122, Mitutoyo Corp., Japan), with a load of 10 N. All tests were conducted at room temperature, and at least five runs were performed.
3. Results and Discussion
3.1. Synthesis and Mechanical Properties of PUA
Chemical reaction of photopolymerization of PUA measured by FT-IR is shown in Figure 2. The peak at about 1650 cm−1 corresponding to the stretch vibration of vinyl groups almost disappears after the UV-curing, indicating that the prepolymer is converted into the polymer with a long chain. Network polymer is generally formed by the reaction between intermolecules or intramolecules with vinyl group during photopolymerization. Therefore, the functionality represented to the average number of vinyl group per a molecule is important factor for increasing the crosslinking density of polymer, leading to the enhancement of the storage modulus and glass transition temperature () of polymer film. In this work, the functionality of prepolymer is controlled by the composition ratio between PUA with two acrylate groups () and NVP with five-numbered cyclic group attached to the vinyl carbon (). The average functionality () of prepolymer is determined by the following equation: where is the mole fraction of prepolymer having functionality (). The functionality of each prepolymer is shown in Table 1. Therefore, the prepolymer with has higher crosslinking density than that with .
Typical dynamic behaviors in mechanical properties of the neat polymer films are shown in Figure 3 as a function of prepolymer composition. Regardless of prepolymer composition, the storage modulus curve shows a single point of inflection corresponding to the glass transition temperature (). This indicates that the urethane acrylate and NVP segments are phase-mixed at a segment level. When two segments are immiscible, generally two discrete values will be obtained. The elastic modulus in the rubbery state and the of polymer film increase with increasing the functionality of prepolymer. Namely, it is due to the augment of crosslinking density of polymer. Since the polymers are networked, as evidenced by the existence of a rubbery plateau, the molecular weight between crosslinks () can be calculated based on the ideal rubber theory given by where , , , and are density (1.1 g/cm3), gas constant (8.314 m3·Pa/mol·K), absolute temperature (373 K), and the plateau modulus, respectively [14, 15]. Using g/cm3 and plateau values of Figure 3, was calculated (see the table in the Figure 3). is decreased from 922 to 525 with increasing the functionality of prepolymer, inducing the increase in the and elastic modulus of polymer film.
The stress-strain behavior of the neat polymer films prepared with different compositions of prepolymer is shown in Table 1. The tensile strength of polymer films is enhanced with increasing the functionality of prepolymer, while the elongation at breaking point decreases, owing to an increase in the crosslinking density. High crosslinking density provides the rigidity in the polymer film and disturbs the chain folding, resulting in the high elastic modulus and the low strain at breaking point in the glassy state.
3.2. Microstructure and Mechanical Properties of PUA-Al2O3 Composites
The presence of PUA in the porous matrix is investigated using FT-IR (Figure 4). In the PUA-Al2O3 composites (runs 2 and 3), the peaks at 2800 cm−1 and 1700 cm−1 corresponding to the C–H aliphatic and conjugated C=O groups, respectively, are detected, which are indicated by arrows in Figure 4. The evidence means that PUA is infiltrated into the porous Al2O3 matrix because these peaks are shown in PUA molecule.
The microstructures of fracture surfaces in PUA-Al2O3 composites with different compositions of prepolymer are shown in Figure 5. In the pure Al2O3 matrix, the Al2O3 particles are almost distinguishable and independent (Figure 5(a-1)), whereas interfaces between Al2O3 particles in the PUA-Al2O3 composites are continuously connected irrespective of the functionality of prepolymer (Figures 5(b-1) and 5(c-1)). The porosities of composites prepared are shown in Table 2, indicating that the porosity of composite is decreased with the increase of the functionality of polymer infiltrated in the matrix, as shown in SEM morphology of Figure 5. In addition, the size of pore existed in the matrix is significantly reduced in the PUA-Al2O3 composites, compared with the pure Al2O3 matrix, which is indicated with white solid arrows in Figure 5. It is provided that the prepolymer with a low viscosity is well infiltrated into the porous matrix. In the low magnification of Figure 5, the fracture surfaces of the pure Al2O3 matrix show considerably rough and uneven, compared with those of PUA-Al2O3 composites. In addition, Al2O3 particles are remarkably aggregated in the pure Al2O3 matrix. However, the fracture surfaces of PUA-Al2O3 composites become smooth and the aggregation between Al2O3 particles is gradually declined with increasing the functionality of prepolymer. Namely, SEM images investigate a good adhesion of the polymer to the ceramic matrix. Therefore, in the case of PUA-Al2O3 composites, the crack propagation through the matrix could be obstructed at the polymer phase , improving the mechanical properties in the PUA-Al2O3 composites.
The elastic modulus and fracture strength values of PUA-Al2O3 composites with different compositions of prepolymer are shown in Figure 6. The composite prepared with the prepolymer composition of 3/1 shows the highest fracture strength and elastic modulus of about 8.5 MPa and of about 9.9 GPa, respectively. In the case of PUA-Al2O3 composites, the fracture strength and elastic modulus are enhanced, compared with those of the porous Al2O3 matrix without the polymer. It is owing to the crack energy (stress energy) dispersed by the polymer and the reduction of porosity. Namely, the crack propagating in the matrix is deflected and/or obstructed at the polymer. Also, the fracture strength and elastic modulus are increased with increasing the functionality of polymer. This enhancement is related to the increase in the crosslinking density of polymer. However, hardness is not changed in spite of the addition and functionality of polymer (see Table 2). It is because the polymer is very lower hardness value than the matrix.
The PUA-Al2O3 composite has been fabricated by infiltration method to improve the mechanical properties of porous Al2O3 matrix. Especially, the interpenetrating network (IPN) method, usually used to increase the universal properties of matrix, is introduced to homogeneously disperse the polymer into the matrix, as a function of the functionality of prepolymer. The tensile strength and elasticity of neat polymer films are increased with increasing the functionality of prepolymer related to the crosslinking density. The microstructure of fracture surface shows a good adhesion between the polymer and the matrix. The PUA-Al2O3 composites have higher values in the fracture strength and elastic modulus than the porous matrix without the polymer, since the crack propagation from intrinsic defects formed at the surface and in the inside matrix is interrupted by the polymer. Therefore, the mechanical properties are improved by the distribution of stress between heterophases in the PUA-Al2O3 composite and enhanced with increasing the functionality of polymer.
This work was supported by the National Research Foundation of Korea (NRF) Grant funded by the Korean Government (MEST) (2011-0030802), by the Korea Institute of Materials Science (KIMS) in 2012, and by the Changwon National University in 2011.
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