Studying the Effect of ZnO on Physical and Elastic Properties of (ZnO)x(P2O5)1−x Glasses Using Nondestructive Ultrasonic Method

Amin Matori, Khamirul; Mohd Zaid, Mohd Hafiz; Quah, Hock Jin; Abdul Aziz, Sidek Hj.; Abdul Wahab, Zaidan; Mohd Ghazali, Mohd Sabri

doi:https://doi.org/10.1155/2015/596361

Advances in Materials Science and Engineering

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Abstract Introduction Results and Discussion Conclusion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2015 | Article ID 596361 | https://doi.org/10.1155/2015/596361

Studying the Effect of ZnO on Physical and Elastic Properties of (ZnO)_x(P₂O₅)_1−x Glasses Using Nondestructive Ultrasonic Method

Khamirul Amin Matori,^1,2Mohd Hafiz Mohd Zaid,¹Hock Jin Quah,³Sidek Hj. Abdul Aziz,¹Zaidan Abdul Wahab,¹and Mohd Sabri Mohd Ghazali⁴

Academic Editor: Baibiao Huang

Received23 Sept 2014

Revised15 Dec 2014

Accepted16 Dec 2014

Published06 Jan 2015

Abstract

Binary zinc phosphate glass system with composition of (ZnO)_x(P₂O₅)_1−x, ( = 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6 mol%) was successfully prepared using a conventional melt-quenching method. Composition dependence of physical properties and elastic properties in the (ZnO)_x(P₂O₅)_1−x were discussed in association with the effects of adding zinc oxide (ZnO) as a modifier. The addition of ZnO modifier was expected to produce substantial changes on physical properties of the phosphate glasses. An increase in density values of the phosphate glasses was observed. Elastic moduli were studied by measuring ultrasonic longitudinal and shear velocities ( and ) of the glasses at room. Longitudinal modulus, shear modulus, bulk modulus, Young’s modulus, Poisson’s ratio, and Debye temperature were derived from both data of velocities and respective density of all of the samples. Findings from present work showed dependence of density and elastic moduli of each ZnO-P₂O₅ series on glass composition.

1. Introduction

Phosphate glasses have been extensively studied due to their interesting properties, such as high thermal expansion coefficient, high gain density, low melting point, low refractive index, low dispersive and transparency ability in a wide spectral range (from UV to IR), as well as potential applications in many industrial fields, which made the phosphate glass suitable for the fabrication of optical fibers, sensor, and laser technologies (laser host glasses) [1–5]. However, the poor chemical durability and high hygroscopic and volatile nature limited the phosphate glasses from replacing the conventional glasses in a wide range of technological applications [6–9]. Many researchers reported that properties of the glasses in terms of chemical durability and physical, structural, and elastic properties can be improved by the addition of metal oxides, such as ZnO, PbO, Al₂O₃, TiO₂, and Bi₂O₃ [10–13]. Thus, the phosphate glasses with addition of heavy metal oxide have been found to be used in broad range of applications, such as photonic, bone regeneration and hermetic sealing technology.

In a phosphate glass, phosphorus always stands in a tetrahedral coordination. It is trustworthy from previous works that addition of glass former and/or glass modifier in the phosphate glass will increase density of the glass produced. This has been proven by the addition of lead oxide (PbO) by Matori et al. [13], ferum oxide (Fe₂O₃) by Sidek et al. [14], samarium oxide (Sm₂O₃) by Brassington et al. [15], vanadium oxide (V₂O₅) by Mierzejewski et al. [16], and phosphate glass by Farley and Saunders [17]. Further investigation by other researchers that had studied binary lead phosphate glasses showed an increase in the density and molar volume as PbO was added to the phosphate network system. The addition of PbO and a decrease in the P₂O₅ concentration in the glass network would cause the densities to increase. This indicated that the Pb²⁺ might act as a network modifier, which altered structure of the glass by reducing nonbridging oxygens (NBOs) in the network and causing the structure to become more compact [13]. Sidek et al. on the other hand studied the effects of ZnO addition on thermal properties of tellurite glass. Experimental results showed an increase in density and thermal expansion coefficient as more ZnO content was being added to the tellurite glass network with a decrease in glass transition, Debye temperature, and softening temperature. The decrease was believed to be related to a change in coordination number of the glass network and destruction of the network structure by the formation of some NBOs atoms [18]. In addition, Kim et al. studied the effects of ZnO addition on photoluminescence of the phosphate glass [19]. It was disclosed that the zinc phosphate glasses were chemically durable with a processing temperatures below 400°C. Hence, zinc phosphate glasses have been used as nuclear waste hosts due to their high chemical durability and low processing temperature [20]. Le Saout et al. characterized the structure of (PbO)_x(ZnO)_0.6−x(P₂O₅)_0.4 system using ³¹P NMR, Raman, and infrared spectroscopies. The investigations revealed no significant change in the average chain length composed of PO₄ tetrahedral units with the substitution of Zn for Pb cation [21].

In this study, ZnO is added to the phosphate glass network as a glass modifier to improve chemical durability of the glass. The resulting zinc phosphate glasses would be interesting for study since the glass phase can be formed over a wide range of concentrations. Moreover, the ZnO can enter the glass network, both as network modifier and as a network former [22, 23]. It was also suggested that a dramatic improvement in chemical durability of the phosphate glasses was associated with the formation of P–O–Zn bond after the addition of ZnO into the phosphate network [24]. In order to further investigate the effects of ZnO addition into the phosphate glass system, physical and elastic properties of the zinc phosphate glass network are of concern in this work. A short-term significance of this work is to establish a baseline for the elastic properties of the phosphate glass with the addition of ZnO into the glass network.

2. Experimental Details

Glass batch of (ZnO)_x(P₂O₅)_1−x binary zinc phosphate (where = 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6 mol%) was prepared using conventional melt-quenching method. All the glass samples were prepared from commercial powders by mixing specific weights of the batches using zinc oxide, ZnO (99.99%, Assay, Alfa Aesar, Ward Hill, MA, USA), and phosphorus pentoxide (P₂O₅) (97.00%, Technical grade, Alfa Aesar, Ward Hill, MA, USA) weighed in appropriate quantities according to the mol% of the composition in glass samples. The mixture was ground using an agate mortar to obtain good homogeneity.

The mixture was then placed into an alumina crucible and heated at 1100°C in a box furnace for an hour. The molten mixture was then quickly poured into a stainless steel mould at room temperature. The glass samples were annealed at 350°C ( of zinc phosphate glass in the range of 280°C to 370°C) for an hour before the furnace was switched off in order to remove the thermal strain [23]. The glass samples were allowed to cool down in situ at room temperature for a day. Later, the glass samples were cut (dimensions of ~10 mm × 20 mm) by using an Isomet Low Speed Saw machine (Buehler) and polished using fine sand paper to obtain flat, parallel end faces that were suitable for ultrasonic measurements.

Density measurement was performed using the Archimedes method with acetone as the buoyant liquid: where is the glass sample weight in air, is the glass sample weight in acetone, and is the density of acetone. All of the glass samples’ weights were measured with a digital balance (±0.0001 g accuracy). The molar volume was calculated using the relation of , where is the molar weight and is the density of glass. Ultrasonic measurements were performed at room-temperature by pulse superposition technique using an Ultrasonic Data Acquisition System (Matec 8020, Matec Instruments, USA) at 10 MHz via x-cut and y-cut quartz transducers with a burnt honey used as a bonding material between the glass samples and the transducers. By measuring thickness of the glass sample (), the longitudinal () and transverse () wave velocities can be measured and calculated using the relation . The absolute accuracy in the measurement of the velocity is ±5 ms⁻¹, and the relative error is ±0.1%.

In an amorphous solid, elastic strain produced by small stress can be described by two independent elastic constants, and . Elastic moduli were calculated using the following standard relations [17]:

3. Results and Discussion

The prepared zinc phosphate ((ZnO)_x(P₂O₅)_1−x) glasses were subjected to ultrasonic measurements at room temperature. Table 1 presents the value of density (), molar volume (), sound velocities (both longitudinal () and transverse ()), the calculated elastic constants ( and ), bulk modulus (), Young’s modulus (), Poisson’s ratio (), and Debye temperature () for the investigated samples. When a higher mol% of ZnO was added to the phosphate glass system, an increase in the density () of the glass system from 2420 kg m⁻³ to 3281 kg m⁻³ was observed (Figure 1). The values of the density measurement are near to other researches [19, 21]. This was due to the reduction of P₂O₅ concentration in the glass network, whereby the Zn²⁺ would act as a network modifier, to reduce the number of nonbridging oxygens (NBOs) in the glass structure and a more compact glass was formed. The possible reactions in the glass network can be represented as follows: The additional oxygen sharing and charge balance requirements are met by the conversion of P=O in [POO_3/2] units to form P–O in [PO_4/2]⁺ units. Therefore, continuous titration of P=O bonds was needed in order for the Zn to be incorporated into the glass network and formed P–O–Zn linkages [23].

Figure 2 shows that the molar volume of the glasses is decreased as the content of ZnO is increased. Generally, an opposite trend for the density and molar volume of the investigated samples were observed in this work, which was in agreement with previous reported results [25, 26]. A decrease in molar volume of the (ZnO)_x(P₂O₅)_1−x glasses from 56.2 cm³mol⁻¹ to 32.2 cm³mol⁻¹ was observed due to the substitution of phosphorus by zinc. Since the radius of Zn²⁺ (0.074 nm) was greater than P⁵⁺ (0.038 nm), the addition of ZnO into the glass system has caused an increase in the bond length or inter-atomic spacing between the atoms, whereby the glass network will expand and form more pores.

Zn²⁺ ions might enter the glass network interstitially to break the P–O–P bonds that might lead to the formation of ionic bonds between the Zn²⁺ and single bonded oxygen atoms. So if one assumed that the only effect of adding Zn cations was to break down the network bonds P–O–P, then the decrease in the molar volume with ZnO content would be expected for the entire vitreous range of the studied glass system. Therefore, the compactness of the glass will increase and reduce NBO’s, which increased the rigidity of the glasses [27].

The longitudinal () and shear ultrasonic () velocities in binary zinc phosphate glass systems with different mole fractions of ZnO content are depicted in Figure 3. The changes of glass structure were depending on the propagation of both longitudinal and shear wave velocities in the bulk samples. Hence, filling of Zn²⁺ ions into the phosphate glass network would result in the glass structure being more compact and rigid. As a result, both velocities and were increased from 3887 m s⁻¹ to 4376 m s⁻¹ and 2406 m s⁻¹ to 2506 m s⁻¹, respectively. It can be seen that the values of are higher than . The increase of ultrasonic velocities with the increase of ZnO concentration has been observed, indicating that ZnO plays a dominant role in the velocities. The increase in ultrasonic velocity of the studied glass revealed the fact that the addition of ZnO to the phosphate glass would cause a swift movement of the ultrasonic wave inside the network of the glass structure. Due to this factor, the ultrasonic velocity of the glasses would increase as the ZnO content was increased. In this (ZnO)_x(P₂O₅)_1−x glass system, ZnO functioned as a network modifier. The ZnO would modify the glass structure, making a glass harder.

The independent elastic constants for isotropic solids and glasses are longitudinal modulus () and shear modulus (), where calculation for other elastic constants and Poisson’s ratio depend on the density and both the velocities values. Young’s modulus () determined from the sound velocity was defined as a ratio of the linear stress over the linear strain [27], whereby this Young’s modulus was related to the bond strength of the materials. The bulk modulus () was defined as the changing in volume when a force is acted upon it at all directions [28].

Figure 4 shows the variation of elastic moduli: , , , and versus mol% of ZnO. The values of elastic moduli were showing an increasing trend with the increase of ZnO content. The attainment of a higher value of than indicated that the (ZnO)_x(P₂O₅)_1−x glasses were able to withstand a higher longitudinal stress than transverse stress. The increase in and was due to the changing in the coordination number with an increasing in the ZnO content. A comparison between and () indicated that the samples were more tolerant to the stress from one direction than the stress from all directions. Since the addition of ZnO would increase the rigidity of glass structure, the velocity and elastic moduli would also increase.

The obtained Poisson’s ratio from the elastic moduli is shown in Figure 5. Poisson’s ratio obtained from the glasses was affected by the crosslink density of the glass structure. An increase in Poisson’s ratio from 0.189 to 0.256 as a function of ZnO content suggested that an equal amount of stress was applied throughout the whole range of the glass composition and the lateral strain was gradually leveled out [29]. In addition, the observation made in Poisson’s ratio supported that there were changes in cross link densities. A continuous increase in the Debye temperature was observed as more ZnO was added to the glass system (Figure 6). This was an indication that the obtained Debye temperature from the ultrasonic velocity data was sensitive towards the amount of ZnO content in glass system, whereby the packing structure of the glass became more compact due to the reduction of NBO’s as the ZnO content was being increased.

4. Conclusion

As a conclusion, a series of binary (ZnO)_x(P₂O₅)_1−x, zinc phosphate glass systems have been successfully prepared and characterized. Based on the results, it showed that the densities increased when ZnO content was added to the phosphate glass systems, while a molar volume was decreased. The increase in density was also probably caused by a change in crosslink density and coordination number of Zn²⁺ ions. The addition of ZnO and a decrease of the P₂O₅ concentration in the glass network caused the densities to increase, indicating that the Zn²⁺ had served as a network modifier and altered structure of the glass by reducing NBOs in the network, and thus the structure turned out to be more compact. The decrease in the molar volume might be attributed to a decrease in the bond length or interatomic spacing between the atoms. The velocities ( and ), elastic moduli (, , , ), Poisson’s ratio, and Debye temperature showed a gradual increasing trend as ZnO was being added to the phosphate glass network. The dramatic increase in ultrasonic velocity and elastic moduli was suggested to be caused by the increase in rigidity and change in coordination number as a result of the decrease in the NBO’s, as revealed by density measurement.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The researchers gratefully acknowledge the financial support for this study from the Malaysian Ministry of Higher Education (MOHE) through the Fundamental Research Grant Scheme. The author (Hock Jin Quah) would like to acknowledge the financial support provided by Universiti Putra Malaysia (UPM) under UPM Post-Doctoral Fellowship Scheme.

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Copyright © 2015 Khamirul Amin Matori 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.

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