Thermally Stable Forms of Pure Polyaniline Catalyzed by an Acid-ExchangedMontmorillonite Clay CalledMaghnite-H + as an Effective Catalyst Rahmouni Abdelkader

Polyaniline salt form (PANI-ES) was synthesized by oxidative polymerization of aniline using potassium persulfate as an oxidant and an acid-exchanged montmorillonite clay called Maghnite-H+ as an effective catalyst. The clay, which was used as a catalyst, was supplied by a local company known as ENOF Maghnia (Western Algeria). The chemical stability of PANI has been investigated by thermogravimetry and differential scanning calorimetry, that a good thermal stability of PANI could be improved by combining PANI with montmorillonite. TGA results illustrated that there were two major stages for weight loss of the ES-form PANI powder sample. The different forms of PANI were characterized by infrared spectroscopy, thermal analysis, and H-NMR spectroscopy and conductivity measurements.


Introduction
As a new organic metal and electrically conductive material, polyaniline continues to attract extensive attention from scientists and engineers although its chemical synthesis was reported almost one century ago [1].Polyaniline is environmentally stable and inert.It has a wide range of potential technological applications including storage batteries, electrochromic devices, light emitting diodes, corrosion inhibitors, and a variety of sensors including chemical [2].Polyaniline has been combined with inorganic materials such as montmorillonite [3].In recent years layered silicates or clays have found their way for being used as fillers for polymers to increase many properties including tensile strength, modulus, barrier, thermal stability, and ignition temperature [4].The polymerization of polyaniline was induced in heterogeneous phase by Maghnite-H + under suitable conditions.Maghnite-H + is a montmorillonite sheet silicate clay exchanged with protons [5].Researchers have demonstrated that the introduction of only a small amount of clay into the polymer structure of polyaniline can lead to a significant enhancement of its properties [6].Therefore, the aim of this paper is to improve the thermal stability of polyaniline through the synthesis with layered materials.The thermogravimetric analysis and differential scanning calorimetry demonstrated the improved thermal stability of the intercalated nanocomposites relative to the pure polyaniline due to the incorporated Na + -montmorillonite.This paper reports the properties of a series of PANI-Mag composites which were prepared by emulsion polymerization of aniline in the presence of a Maghnite substrate.The proposed process for the polymerization is show in Scheme 1.Based on the TGA and DSC results, thermal aging experiments were designed to study the thermal reactions of PANI-ES, PANI-EB, and PANI-HCL by infrared spectroscopy, UV spectroscopy, and H 1 -NMR spectroscopy.

Thermogravimetric Analysis (TGA).
The tests were performed on a TA instrument (TGA Q500) by heating the samples from 20 to 550 • C at 20 • C/min, with DTG thermograms giving the variations of the weight loss derivative as a function of temperature.

Preparation of Maghnite-H + .
Maghnite-H + was prepared according to the process reported in our previous study [10].Raw Maghnite (20 g) was crushed for 20 mn using a prolabo ceramic balls grinder.It was then dried for 2 h at 105 • C. The Maghnite was placed in an Erlenmeyer flask together with 500 mL of distilled water.The Maghnite/water mixture was stirred using a magnetic stirrer and combined with 0.25 M sulfuric acid solution, until neutralization was achieved over 2 days at room temperature, the mineral was then washed with distilled water to become sulfate-free and then dried at 105 • C.

Synthesis of Different Forms of Polyaniline.
Polyaniline salt (PANI-ES) was synthesized by the chemical oxidation of aniline with potassium persulfate (K 2 S 2 O 8 ), water, and montmorillonite (Mag-H + ) and the mixture was precooled to below 0 • C in an ice bath.5.1 mL of (0.055 mol) aniline was added to 6% of (0.356 g) Mag-H + clay catalyst layered.The reaction was stirring for 30 mn at 0 • C, after this time 3 g of (0.013 mol) oxidant was added slowly during 10 mn, after this we added drop by drop 15 mL of water.The reaction was continued for 1 h and 30 min in the optimal condition (0 • C).
The precipitate product was filtered and washed with distilled water as far as neutralization, because this product contained traces of initiator, oligomer, and monomer.In the end, we obtained black solid which is composed of polymer-Mag.However, the Mag-H + is separated by filtration because it's insoluble in the solvents in which the polymer is soluble.
Eventually, the resultit's black solution (polymer-solvent), after evaporation result a black powderit's (PANI-ES), washed several times with water and methanol, where dried at 60 • C for 48 h for characterization.
The polyaniline base (PANI-EB) is obtained by deal treatment of polyaniline salt (PANI-ES) with a solution of dilute NaOH (0.5 M).Then, the prepared ES-form PANI was converted to EB-form PANI by stirring with 200 mL of 0.5 M NaOH dilute solution at room temperature for 5 to 10 hours.At the end of the stirring, the PANI-EB was filtered, washed with water and methanol several times, and dried under vacuum at 60 • C for 48 hours by characterization.

Results and Discussion
3.1.FTIR Spectral Analysis.The FTIR spectra of the PANI-ES and PANI-EB under the same conditions were shown in Figures 1 and 2. The FTIR spectroscopy evidence the formation of polyaniline structure containing 1,4-paradisubstituted linear chain.The vibration frequencies of the major infrared bands and their assignment for polyaniline PANI-ES and PANI-EB are summarized in Table 1.

1 H-NMR Spectral Analysis.
The 1 H-NMR spectra of the PANI-ES and PANI-EB polymers exhibit strongest sharp peak centered at 7 ppm and 7.8 ppm due to protons on phenylene and disubstituted phenylene units, the weak peak at 4.81 ppm and medium broad peak at 6.22 ppm due to (-NH-and -NH 2 ) end group, respectively.Other broad peaks centered at 1.78 ppm and 8 ppm may be due to the water protons bonded by (-NH-and -NH 2 ) groups and (H-N + ), respectively, as shown in Figures 3 and 4 [11].

Thermal Analysis
(A) Thermal Analysis of Maghnite-Na + .The thermal characterizations of the composites include thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC).Weight losses (%) versus temperature ( • C) curves for pure Maghnite-Na + are shown in Figures 5 and 6.In Figure 5, the TGA of pure Maghnite-Na + shows two stages of weight loss.The first weight loss in Na + -Mag below 100 • C is a result of the release of free water.The second weight loss around 600 • C is associated with the dehydroxylation of silicate structure [12,13].The total weight loss is only 13.94% up to 800 • C. As can be expected, Maghnite-Na + shows a high thermal stability.• C/min in nitrogen is shown in Figure 7.It can be found that at the temperature range of 187-600 • C the weight loss amounted to 61, 17%, which can be reasonably attributed to the weight loss of the polymerized polyaniline (PANI-ES) and to thermal decomposition of the polyaniline chains.
Polyaniline is known to be a hygroscopic polymer [14].Some authors [15] assigned the endothermic effect registered by DSC in the range from ambient temperature up to approximately 120 • C to the evaporation of water.Figure 8 is the DSC thermogram of the PANI-EB form powder in the first run and second run.In the first run there were two endothermic peaks at 55.99 and 103.46 • C and the PANI-EB powder had discernible moisture content [16].Therefore, these endothermic peaks were most likely due to the evaporation of water.This was in agreement with the TGA results.
In the second run, there were almost no significant endothermic or exothermic peaks, as shown in Figure 8, because no apparent moisture existed in the sample but Tg appear at 74.06      [17].For more information such as stability, conductivity, solubility, chemical structure, and morphology of different form of polyaniline, Table 2 shows the thermodynamics properties of different states of polyaniline.(1) Initiation (see Scheme 2).The mechanism of the reaction occurs within the layers of the Maghnite exchanged by H + protons, which are capable of initiating cationic polymerization in the presence of the oxidant K 2 S 2 O 8 .
(2) Propagation (see Scheme 3).Propagation is by the successive addition of monomers on the chain macromere growing.
(3) Termination (see Scheme 4).The termination takes place during the recombination of two radical ions giving rise to the final polymer.

Conclusion
Polyaniline has been intensively studied recently due to its various properties as well as to its environmental stability.The thermal behavior of polyaniline PANI-ES, PANI-EB, and PANI-HCl were studied using thermogravimetric analysis and differential scanning calorimetry.The montmorillonite clay has received intensive attention because it is natural, abundant, cheap, and has high chemical resistance.Therefore, the aim of this paper is to improve the thermal stability of PANI through the synthesis with layered materials.Although the polymer is black, which could be identified as PANI-ES.
It has been proved that Mag-H + can be used to induce the polymerization of aniline, and this offers new possibilities for the selective study of montmorillonite as catalysts and for the synthesis of polymers conductors such as polypyrrole, polythiophene, polyaniline, and there derivates.

Figure 7 :
Figure 7: TGA curves of a pure PANI-ES obtained in nitrogen atmosphere at heating rate of 10 • C/min.

6 International
• C. First run and second run in Figures 9 and 10 show the DSC cooling trace of the PANI-ES and PANI-HCl.Two remarks can be observed.(a) Three endothermic peaks; these Journal of Polymer Science

Figure 9 :
Figure 9: DSC curve of the PANI-ES composite obtained in nitrogen atmosphere at heating rate of 10 • C/min.

Figure 10 :
Figure 10: DSC Curve of the PANI-HCl composite obtained in nitrogen atmosphere at heating rate of 10 • C/min.

3. 4 .
Proposed Mechanism of the Reaction.The proposed mechanism of cationic polymerization of (PANI) catalyzed by Maghnite-H + .

Table 1 :
The vibration frequencies of PANI-ES and PANI-EB.