Synthesis of Electroconducting Hydroxy-Sodalite / Graphite Composite : Preparation and Characterization

Electroconductive hydroxy-sodalite/graphite composites were synthesized by alkali-activation of kaolinite in the presence of sodium hydroxide as the alkali activator and graphite as a conductive filler. Thermal, morphological and microstructural properties in addition to direct current (D.C.) conductivity of the prepared composites were investigated. Thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy in the attenuated total reflection mode (FTIR/ATR), X-ray diffraction (XRD), scanning electron microscope/energy dispersive using X-ray analysis (SEM/EDX) and DC conductivity measurements were used to characterize the prepared composites. The effect of the hydroxyl-sodalite-to-graphite and NaOH-to-kaolinite ratios on the electrical conductivity was investigated and evaluated on the generated composite specimens made of Jordanian kaolinite or pure kaolinite. It was demonstrated that increasing the mass ratio of graphite-to-kaolinite in the clay-based composites increased the electrical conductivity of the resultant composites. It was also observed that using 1:1 graphite-to-pure kaolinite mass ratio showed the best electrical conductivity value of 3 × 10 s/cm, among the other mass ratios used for pure kaolinite specimens, while using 1:1 mass ratio of graphite-to-Jordanian kaolinite showed a conductivity of 1.6 s/cm.


Introduction
Inorganic polymers are macromolecules comprising of inorganic elements as part of their skeletal structure or as pendent functionality within a dimensional skeletal structure [1].The term inorganic polymer is more often used to specify polymers without carbon atoms in their skeletal structures.Inorganic polymers have attracted the attention of researchers on the unique properties of the inorganic counterpart in the polymer as compared to their organic counterparts [2].
The excellent features of the inorganic polymers include high thermal stability, inexpensive versatile sources, high mechanical strength, and the ability to be manufactured in chains, sheets and three-dimensional structures [2] [3].
The reaction of solid aluminosilicate sources, such as kaolinite, with an aqueous alkali hydroxide or silicate solution can produce a synthetic alkali activated aluminosilicate material, which is called inorganic polymers.Sources of solid aluminosilicate include natural minerals such as kaolinites and industrial wastes such as fly-ash and slag from blast furnaces [5].The alkali activation reaction is pH sensitive and NaOH or KOH may have been frequently used for this specific purpose [6] [7].
Hydroxy-sodalite is a crystalline form of aluminosilicate network comprising of diverse ordered channels, sizes and infinite structures [4] [8].This particular channel-like structure is responsible for many applicable properties of the H-SOD, such as molecular sieving [9], catalytic activities [10], ion exchange [11], and high selectivity for adsorption [12] [13].Using naturally occurring aluminosilicate materials such as kaolinite can reduce further CO 2 emissions produced from thermally activated aluminosilicates [14].Aluminosilicate polymers have many enticing properties such as malleability, and ability to be molded in various complex shapes and to be intercalated with different conductive additives, such as carbon nanotubes, graphite powder and metal nanowires [15].Graphite, on the other hand, has a two-dimensional carbon skeletal structure, famed with lubricating and electrical properties and is commercially made from charcoal or coke.Intercalating compounds with graphite can give superior metallic anisotropic properties [16] [17].In the unique sandwiched structure, the host atom or molecule is located between the graphite layers, generating compounds with variable stoichiometries in which the atoms are covalently bonded in the plane with only three of the four potential bonding sites persuaded.The fourth electron is left free to travel through the planes of the carbon layers in graphite, providing vast electron delocalization; hence electrical conductivity.
Graphite is the most stable form of carbon-based structure under standard conditions and has high thermal stability and high electrical conductivity.These desirable properties have led to its widespread utilization in high temperature ma- In this study, the synthesis of a hydroxy-sodalite/graphite composite was done by an alkali activation of kaolinite.The reaction was conducted at a low temperature and pressure in the presence of sodium hydroxide as the alkali activator.
The effect of the hydroxyl-sodalite-to-graphite and NaOH-to-kaolinite ratios on the electrical conductivity was investigated and evaluated on the generated composite specimens made of Jordanian kaolinite or pure kaolinite.

Preparation of Materials and Standards
Jordanian kaolinite rich clay (coded as JK) was collected from Batn elgoul (south of Jordan).As a reference, pure kaolinite clay (coded as PK) was supplied by Merck KGaA (99.99% minimum purity, Germany).Graphite powder with an average diameter size ≤ 150 μm (99.99% minimum purity, Sigma Aldrich) was used as the conductive phase in the composite.The alkaline activating solution was prepared by adding a certain amount of NaOH pellets (98% pure, Merck KGaA, Germany) to Milli-Q integral water in a capped plastic bottle.The sodium hydroxide solution was left to cool down to ambient temperature prior to use.
The graphite/kaolinite powder with different mass ratios was mixed thoroughly with NaOH solution, as listed in Table 1.To ensure enough workability and stability for molding and de-molding of the specimens, a planetary mixer (Hobart A200) was used at 198 rpm for 10 min.The formed viscous dark mixture was molded immediately in a stainless steel cylindrical mould (with a diameter of 2.5 cm) using a hydraulic press at a pressure of 5 -6 MPa.The dimensions of the specimens after hydraulic pressing were measured using a digital caliber to be nearly 18 -23 mm in height.The molded specimens were then cured Advances in Materials Physics and Chemistry in an oven (Heraeus model TU100/150) at 75˚C, which is well below the boiling point of water, for 2 -3 days to prevent the high vapor pressure of water which may disrupt the specimens and affect the strength of the composite body.

Characterization of the Raw Materials and Prepared Composites
The chemical compositions of the pure and Jordanian kaolinites, graphite powder and the resulted inorganic polymer composites were examined on fused pellets using Shimadzu XRF-1800 sequential equipped with Rh anode X-ray tube.The mineralogy of the samples was determined by X-ray diffraction (XRD) analysis using Shimadzu MAXima XRD-7000 diffractometer with a Cu Kα-radiation (λ = 1.54 Å, 40 kV, 40 mA) at a scan rate of 2 degree/min and a 2θ range of 2˚ -7˚.The receiving slit used was 0.3 mm and step scan size 0.02 degree/step.
The produced composites were crushed and sieved down to a diameter of ≤250 μm prior to characterization experiments using a manual mortar and a micro-filter for sieving.Thermogravimetric analysis (TGA) was used to investigate the thermal stability and dehydration of the composites prepared from different NaOH mass ratios by using a NETZSCH (STA 409 PG/PC thermal analyzer).The prepared samples were analyzed promptly by TGA in an isothermal process at 40˚C for 1 h to investigate any mass losses that were associated with free or adsorbed water present in the composites.Then about 35 mg of the composite sample was heated from 50˚C to 1000˚C at a rate of 10˚C min −1 under a nitrogen gas atmosphere.
The infrared (IR) spectra were obtained for the composites prepared from different NaOH mass ratios using a thermo scientific Nicolet spectrometer (Thermo Scientific Smart iTR-IS50R), coupled with an attenuated total reflectance diamond crystal unit.The IR spectra were collected and averaged over 32 total scans from 4000 to 650 cm −1 at a resolution of 2 cm −1 .
The morphology of the prepared composites was evaluated by using scanning

Electrical Conductivity Measurements
The composite samples were subjected to electrochemical current-voltage (I-V) characterization at room temperature using (EG&G) Princeton Applied Research scanning potentiostat (Model 362, USA) instrument with a two-electrode system interfaced to computer software for control and data acquisition.The potential window used was between −0.9 and +1.7 V and a scan rate of 50 mV/S was used in this measurement.The inorganic polymer specimens were connected to the potentiosatat electrodes and their electrical conductivities were measured.
The thickness of the specimens was measured by using a digital caliber.The electrical conductivity ρ was calculated according to the following Equations ( 1) and ( 2): where R is the electrical resistance, l is the length of the cylindrical specimens and A is the cross-sectional area of the cylindrical specimen, V is the applied voltage and I is the measured current.

Results and Discussions
The TGA curves of the prepared composite materials showed that the major mass loss steps occurred above 500˚C (Figure 1(A) and Figure 1(B)).The derivative curves are also shown here to give a better comparison among the samples.The first mass loss located at 70˚C is nearly identical for graphite and the composites which attributed to free or adsorbed water.The second mass loss step started from 400˚C to 700˚C is attributed to the de-hydroxylation of un-reacted kaolinite.The magnitude of this broad peak is found to be increasing with the increase in NaOH concentration up to 800˚C, indicating a full transformation of kaolinite samples during the alkali activation [4].
The IR spectra in Figure 2(A) and Figure 2(B) show remarkable differences in the three main wave numbers regions: The bands located at 650, 750 and 780 cm −1 are corresponding to the Al-O bending mode of AlO 6 octahedra in kaolinite [24] [25].They showed a reduction in the peak intensity which reveals the disintegration of the genuine octahedral structure of the kaolinite particles [4].Two distinctive weak absorption bands appeared at 730 and 660 cm −1 .These two bands are associated with zeolitic phases in the composite, which were reported for the bands observed at 731 and Advances in Materials Physics and Chemistry The chemical compositions of PK and JK samples are listed in Table 2.The PK powder is composed mainly of 47.8% SiO 2 and 36.1% Al 2 O 3 that makes it suitable for H-SOD synthesis [14].
The    phase of H-SOD in the composites.H-SOD crystallites accumulated and bonded to the reacted surface of the composite.Figure 4(C) illustrates that the surface of the synthesized material is homogeneously covered by H-SOD nano-particles when Jordanian kaolinite was used in the composite preparation.The H-SOD/graphite particles are linked with each other and aggregate to form porous structure on the surface of the material.The composite aggregates are less than 5 μm in diameter, while the single crystallite diameter of the composite is about 700 nm [4].
The electrical conductivity of the composites, obtained from using 0.25, 0.50, 0.75 and 1.00 mass ratios of graphite-to-kaolinite, was measured.Figure 5 shows the variation of the electrical conductivity with increasing the mass ratio of graphite-to-kaolinite.The electrical conductivities of both kaolinite based composites increased when increasing the graphite-to-kaolinite mass ratio.It was also observed that 1:1 graphite:PK composite showed the highest electrical conductivity value of 3 × 10 −3 s/cm among all graphite:PK ratios.When 1:1 graphite:JK ratio was used, the conductivity of the composite even reached 1.6 s/cm.Advances in Materials Physics and Chemistry

R.
Alomari et al.DOI: 10.4236/ampc.2019.9300327 Advances in Materials Physics and Chemistry terial manufacturing applications [18] [19].Electrically conductive clay-based materials are acquiring a substantial debate due to their superior properties over their metallic electroconductive analogues [15] [20].They have attracted great attention in many industrial and scientific areas because of their high chemical, thermal and wear resistances and high mechanical strength as compared to the traditional metal-based electroconductive materials.Moreover, electroconductive clays have a potential to provide higher electrical sensitivity since they have been served as ensemble of microarrays or ultramicroelectrodes, which enhanced the signal and lowered the background noise [15] [21].The electroconductive polymers prepared with aluminosilicate materials might be tailored to specific industrial applications by incorporating conventional functional groups into the aluminosilicate matrix.The resulted materials are of a salutary hybrid since it combines the high mechanical strength of aluminosilicates and the electroconductivity of the filling additives in the material structure.The electrical conductivity of the clays is more often evaluated on a rectangular or cylindrical specimen to affirm the bearing of a uniform electric filed in the specimen material [21] [22] [23].
SEM images and EDX results of the graphite and the kaolinite-based H-SOD samples synthesized at different NaOH/kaolinite mass ratios are shown in Figure 4.The SEM image of the graphite powder (Figure 4(A)) shows the presence of carbon and oxygen atoms, as determined by the EDX spot analysis.

Figure 4 (
Figure 4(B) and Figure 4(C) illustrate that the reaction between graphite powder and different NaOH/kaolinite mass ratios caused an evolution of a new

Figure 4 .
Figure 4. SEM images of (A) graphite (B) pure kaolinite based H-SOD/graphite composite synthesized using different NaOH/clay mass ratio (C) Jordanian kaolinite based H-SOD/graphite composite synthesized using 0.4 NaOH/clay mass ratio.

Figure 5 .
Figure 5. Values of electrical conductivity for different (a) pure kaolinite based H-SOD/graphite composite mass ratios synthesized using different NaOH/kaolinite mass ratio (C) Jordanian kaolinite based H-SOD/graphite composite mass ratios synthesized using different NaOH/kaolinite mass ratio.

Table 1 .
The mass ratios of the components of PK and JK based H-SOD/graphite composites where P1-P4 are codes referring to PK based H-SOD/graphite composites and T1-T4 are referring to JK H-SOD/graphite composites.