Abstract
This work focuses mainly on the preparation and characterization of polypyrrole/organically modified clay nanocomposites. Organoclay/polypyrrole nanocomposites were prepared by oxidative polymerization of pyrrole in aqueous medium using ferric chloride as the oxidant. Initially, cetyltrimethyl-ammonium bromide and tetrabutyl-ammonium hydrogen sulphate were used as organophilic to modify clay and form an organic clay. After that, polypyrrole/organically modified clay nanocomposites were synthesized by in situ polymerization process in which pyrrole was polymerized in the presence of different proportions of organic clay. The effects of the nature of the organic clays and the preparation method were studied in order to evaluate their structural, morphological and thermal properties. X-ray diffraction (SAXS), Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, transmission electron microscopy, were used to define the characteristics of the materials obtained. The obtained results confirm the intercalation of molecules of salt in the clay layers, and good interaction with the polymer. Thermogravimetric analysis showed better thermal stability of nanocomposites compared to pure polypyrrole. The conductivity behaviour of nanocomposites was also examined.
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1 Introduction
In the last decade, a lot of attention has been devoted to the synthesis and application of nanocomposites with a clay-polymer matrix. Polyolefins, such as polyethylene and polypropylene, are the most commonly used polymers for clays containing nanocomposites [1,2,3]. Lamellar clays of the montmorillonite (MMT) type have been the subject of considerable interest for the manufacture of polymer–clay nanocomposites. These inorganic/organic nanocomposites have new and enhancing properties that individual inorganic and organic components do not possess [4,5,6,7,8,9]. Conjugated or conductive polymers have emerged as a highly promising class of materials for various applications. Their physical and chemical properties make them particularly attractive. The main classes of organic conductive polymers are polyacetylenes, polypyrroles, polythiophenes and polyanilines. They could have very interesting applications in the field of electrical and electronic components since they are very light [10], they can be used as organic semiconductors, electroluminescent materials, coatings for magnetic shielding, active energy storage materials, electrochemical systems [11] antistatic and anticorrosive coating materials, sensors and batteries [12]. These polymers are obtained by electrosynthesis, chemical or oxidative processes depending on the application. Polymerisation is a field of application that seeks an efficient way to produce polymers of a renewable nature, for example by using sustainable resources and developing solvent-free polymerisation processes [13]. The purpose of green chemistry is to develop chemical products and processes that reduce or eliminate the use and synthesis of hazardous substances. It is based on several principles. To meet industry standards while respecting the environment, acids have been replaced by another clay-based ecocatalyst called Maghnite. The latter is of the montmorillonite type and has been the subject of several studies [14,15,16]. The clay layer has a hydrophilic character and metamorphoses into organo-clay (surfactant) to facilitate the wetting of the polymer molecule on the clay surface [17, 18]. Miyata et al. [19, 20] studied the typical chemical synthesis of PPy using FeCl3 as oxidant/dopant in various solvents. They considered methanol to be the best solvent for optimal conductivity and morphology. The resulting polymer demonstrated a more harmonious fibrillar morphology and more tense films. Chen et al. [21] it was also possible to prove that the monomer/oxidant ratio established the electrical conductivity and morphology of the PPy thus obtained. Maximum conductivity has been established at a value of 2:1 monomer/oxidant ratio. In this work, we will highlight an ecocatalyst (clay) by modifying it by exchange with organoclay cations by using it in the synthesis of a conductive polymer based on pyrrole. Surfactants are known to have greater dispersive power at much lower concentrations and a singular capacity for self-organization, which will allow their distribution within the clay. The detailed thermal and morphological properties were studied to get a good overview of the main parameters that can be controlled to determine the structure of the nanocomposite and therefore the properties of the nanocomposite PPy/clay. We are going to optimize the pyrrole/clay mass ratios to obtain the best electrical conductivity as this improvement in properties opens great prospects for the use of these materials in the electronics industry. The objective of this work is to use a local montmorillonite type clay, called Maghnite, as an eco-catalyst in this polymerization by studying the effect of an organic clay prepared with different reports on the properties of PPy/Algeria clay nanocomposites.
2 Materials and methods
2.1 Materials
Pyrrole (Py) and cetyltrimethylammonium bromide, tetrabutyl ammonium hydrogen sulphate (TBAHS) and ferric chloride FeCl3 were supplied by Aldrich and used without further purification. Raw-Maghnite: Algerian montmorillonite clay that was used as a catalyst is supplied by a local company. The various chemical elements in the local maghnite were transformed into oxides and analysed by X-ray fluorescence (experiment carried out at the ENOF). These results make it possible to verify that the maghnite used is basically composed of montmorillonite, since the SiO2/Al2O3 ratio is equal to 3.77 and therefore belongs to the family of phyllosilicates.
2.2 Preparation of maghnite-Na+
Sodium ions are often chosen as compensating ions because they are more easily hydrated and promote the swelling and dispersion of montmorillonite in water. A mass of raw Maghnite (10 g) was placed in a volume of distilled water (40 ml), this mixture was left in suspension under magnetic stirring and at temperature ambient for 2 h. After 2 h, a volume (60 ml) of sodium chloride solution (NaCl, 0.2 M) was added to the previous mixture and stirred for 48 h. After this time, the Maghnite-Na + was filtered and washed several times with distilled water in order to remove Cl- ions. After filtration, the Maghnite-Na+ was dried in the oven for 24 h at a temperature of 105 °C, afterwards it is finely ground and stored in a dry place [22, 23].
2.3 Organic modification of clay
Two types of organo-modified clays were prepared by cation exchange, using sodium maghnite and two surfactants: cetyltrimethyl-ammonium bromide (CTAB) and tetrabutyl-ammonium hydrogen sulphate (TBAHS) at different concentrations. A quantity of 10 ml of 1N hydrochloric acid was added to each of the two one-litre volumetric flasks and then the volume was made up with distilled water. The two solutions obtained were then poured into each vial equipped with a magnetic stirrer, and the acid solutions were placed at a temperature of 80 °C. When the temperature became stable, 10−2 mol of cetyltrimethylammonium bromide and tetrabutyl ammonium hydrogen sulfate (TBAHS) were introduced separately into each mixture. After 3 h of stirring at 80 °C, the amine was dissolved and ionized for both solutions. Then 5 g of sodium maghnite were added, after 3 h of cation exchange, the modified maghnite was recovered and rinsed six times in a row with distilled water at 80 °C to remove the mineral cations. The effectiveness of this rinsing was verified by adding a few drops of silver nitrate to the residue. The physisorbed alkylammonium ions were removed with a mixture of water and ethanol, previously heated to 75 °C. The organophilic maghnite obtained was then dried at 120 °C and ground. This method makes it possible to determine two organic clays called Maghnite-CTA+ and Maghnite-TBA+ throughout this study [24, 25].
2.4 Preparation of the nanocomposites
0.53 g (8 mol) of pyrrole monomer (freshly distilled) was introduced into two separate vessels, a mass percentage of modified clays (0.2, 1, 3.5 and 10%) was added to each vessel which is kept under agitation for 30 min to allow the monomer to settle into the clay structure. Next, a Fecl3 polymerisation initiator (0, 1 M) of a 100 ml volume solution was added to the mixture in each vessel with stirring at 400 rpm for 24 h at room temperature (The operating conditions are shown in Table 1). Each nanocomposite obtained at the end of the reaction has been filtered and washed successively with distilled water, methanol and acetone several times until traces of oxidant disappear, eventually, it will be dried at 60 °C [9] (Fig. 1).
2.5 Characterization
The infrared spectra were drawn on a Perkin Elmer IR TWO spectrophotometer equipped with an ATR, in the range 400–4000 cm−2. The X-ray diffraction analysis (XRD) was performed at room temperature in a Bruker D8 Advance X-ray diffractometer (40 kV, 30 mA). Thermogravimetric (TGA) and differential scanning calorimetric (DSC) analyses of clay samples were measured on Shimadzu TGA 51 equipment, using an air flow rate of 50 ml/min and a heating rate of 10.0 °C/min. Transmission electron micrographs (TEM) were performed on a Hitachi 8100. The electrical conductivity was measured using an Ohm meter (Advantest, Digital electrometer, TR8652) (four-point method). The surface morphology of the prepared materials was observed by Scanning Electron Microscopy (SEM) “JEOL 7001F, FEG-SEM”.
3 Results and discussion
3.1 Infrared spectroscopy (IR)
The infrared spectra of the PPyNC nanocomposites prepared by the different organoclays and organophilic Maghnite, Polypyrrole are shown in Fig. 2. These infrared spectra show that virgin PPy and nanocomposites have almost the same vibration bands that overlap with the vibration bands of organically modified clay. The absorption bands at 2925 cm−1 and 2854 cm−1 which are attributed to the valence vibrations of the –CH2 groups, as well as the band at 1544 cm−1 corresponds to the elongation of the C=C bond in the pyrrole ring and the peak at 1271 cm−1 is induced by the C–N stretch. A band is observed at 3450 cm−1 corresponds to the N–H bond of PPy, the results obtained are comparable to those in the literature [26,27,28,29,30,31]. In addition, the bands between 784 and 675 cm−1 also indicate deformation vibrations of N–H in the polymer and the absorption band at 835 cm−1, suggesting several interactions between PPy and the organically modified clay, there is an intense peak at 1057 cm−1 and two bands of 455 and 515 cm−1 related to the elongation and torsional vibrations of the Si–O–Si and Si–O–Al bonds, respectively furthermore the bands of 1440 and 1131 cm−1 confirm the protonation of the nitrogen atom in the polypyrrole. The wide bands at 1643 cm−1 and 3625 cm−1 are attributable to elongations of hydroxyl groups in water linked by hydrogen bonding to clay [32, 33]. Also the characteristic peak of PPy registered in PPy/Mag nanocomposite systems is a strong indication of PPy intercalation in nanocomposite systems.
3.2 X-ray diffraction (XRD)
Figure 3 shows the comparative diffractograms of Mag-Na+, Mag-CTA+(1CEC, 2CEC) and Mag-TBA+(2CEC). The XRD obtained are practically identical and indicate an incorporation of the alkyl chains of the surfactant in the Maghnite galleries. Indeed, for a concentration at 1CEC, the interfoliar distance of Mag-Na+was reduced from 12.7 to 18.16 Å for Mag-CTA+ (1CEC) corresponding to a “bilayer” organization. However, for a concentration of 2CEC, a bimodal profile for Mag-CTA+ (2CEC) is observed centred on two values 19.27 Å and 33.53 Å. Concerning the second surfactant Fig. 3 also shows the Mag- Na+diffractograms exchanged with the prepared TBAHS(1CEC), there is a slight increase in the interfoliar distance indicating an insertion of the surfactant into the Maghnite galleries. This slight increase can be explained by the short alkyl chains (4 carbons) of the surfactant. Thus, TBA+ ions adopt a monolayer conformation.
The series of nanocomposites generated by the in situ polymerization of Py is illustrated in Figs. 4, 5 and 6. The pyrrole is represented by an important peak at 2Ɵ = 24.6°, the peak characterizes the amorphous polypyrrole [34]. These peaks were also detected in nanocomposites with the appearance of additional peaks characteristic of the Maghnite organophilic, confirming its good dispersion in the polymer matrix. All nanocomposites elaborated by Mag-CTA+(1CEC) showed a peak around 2Ɵ ≈ 5.75° corresponding respectively to the distances between the layers d001 ≈ 16.65–18.9 A°. The distance between the layers of these nanocomposites decreased compared to the Mag-CTA+(1CEC), which had a d001 ≈ 18.1 Å. This result confirms the intercalation of PPy in the Mag-CTA+(1CEC). The preparation of nanocomposites by Mag-CTA+(2CEC) showed the displacement of the basal peak d001 at low angles between 2Ɵ ≈ 2.6–2.5°, the distances between the layers being respectively from 34.3 to 33.4 Å thus confirming their intercalated shapes (Fig. 5). Except for nanocomposites prepared with 10% Mag-CTA+(2CEC), the polymerization of Py reveals a partially intercalated structure of low-yielding clay (Table 2), due to the closure of the clay galleries leading to tortuous diffusion pathways, these results are consistent with those obtained in the literature [35]. Similar results were obtained using Mag-TBA+ (1CEC) as a reinforcement in the synthesis of nanocomposites showing intercalated structures (Fig. 6). On X-ray diffractograms relating to 0.5.1% by weight of clay, the nanocomposites PPy/Mag-CTA+(1CEC, 2CEC), PPy/Mag-TBA+(1CEC) (Figs. 4, 5 and 6) show a significant peak corresponding to PPy, however, no clay peak appears, which makes it possible to conclude the presence of an exfoliation of montmorillonite in the polymer matrix.
3.3 Transmission electron microscope (TEM)
Transmission electron microscopy is the most widely used qualitative technique for characterizing polymer–clay nanocomposite dispersions and to confirm the results obtained by DRX analysis, the nanocomposites obtained are illustrated in Fig. 7. The nanocomposite obtained by Mag-CTA+(1CEC) showed an intercalated structure of the modified clay. The TEM image of the nanocomposite NCPPy/Mag-CTA+((1CEC) With 3 wt.% and 10% shows an intercalated morphology (Fig. 7a NC2PPy, b NC4PPy10/Mag-CTA+(1CEC)), which corresponds to the results found by DRX with a presence of small tactoids. In addition, we note the presence of some aggregates. The dark lines correspond to the silicate monolayers. The existence of intercalated clay regions is probably due to the limitation of the diffusion of PPy in organophilic clay layers. Micrographs of the nanocomposites (Fig. 7c NC6PPy3, d NC8PPy10/Mag-CTA+(2CEC)) are in favour of an intercalated morphology that preserves the order of the clay particles. However, micrographs of the nanocomposites NCPPy/Mag-TBA + (1CEC), With 3% by weight and 10% are favourable to an intercalated morphology where the order of the clay particles is maintained (Fig. 7e NC10PPy3, f NC12PPy10/Mag-TBA + (1CEC)). The series of nanocomposites (3, 5 and 10%) developed by Mag-TBA + (1CEC) revealed an intercalated structure, these results are in agreement with those of DRX. On the other hand The TEM image of the PPy nanocomposites with 0.5 and 1% by weight of the modified clay shows an exfoliated morphology, a degree of disorder in the morphology of the clay. The clay platelets are separated from each other which is in favour of an exfoliated structure.
3.4 Thermal stability (TGA)
The TGA curves for PPy and these nanocomposites are shown in Fig. 8. According to the TGA curves, PPy nanocomposites show several levels of degradation, the first being between 50 and 150 °C, which corresponds to the departure or loss of the bound and cross-linked water molecules in the intercalated space. In this temperature range, approximately ≈ 05.06% mass loss, which confirms the hydrophobic character of PPy and organically modified clays. Decomposition of doping anions to PPy begins at 200 °C followed by a large mass loss of 260–630 °C due to the significant thermal degradation of the PPy chains which corresponds to a 50% decrease. For pure PPy, polymer degradation and decomposition begins at 270 °C, and the polymer appears to decompose entirely at 630 °C, while the thermal degradation of NCPPy composites all occurs at close to 262 °C, an increase of 12 °C over virgin PPy. These results clearly show that the thermal stability of the nanocomposites obtained is related to the content and nature of the clay, the state of existence of the clay in the polymer matrix (intercalation or exfoliation), so it can be concluded that the experimental results obtained are in accordance with the literature [36, 37].
3.5 Electrical conductivity
Table 3 shows the following results, the highest electrical conductivity being that of PPy/Mag-CTA + (2 CEC) nanocomposites of the order of 1.41 S/cm, while that of PPy/Mag TBA + (1 CEC) nanocomposites is of the order of 0.61 S/cm. We notice from the table that the electrical conductivity decreases with increasing charge rate in the two nanocomposites PPy/Mag-CTA + and PPy/Mag-TBA + . The results show that good electrical conductivity is obtained using a small amount of organophilic Maghnite for 1% by weight and continues to decrease to 10% by weight (Fig. 9). The decrease in conductivity to 10% of the amount of organophilic Maghnite can be explained by the fact that Maghnite acts as an insulator once its amount is increased. Maghnite acts as an oxidizing support, bearing in mind that the chemical synthesis of conductive polymers in general requires the presence of an oxidizing agent. Montmorillonite hinders the relocation of electrons along polymer chains and limits inter-chain movement.
3.6 Scanning electron microscope
Figures 10 and 11 illustrate the SEM images of the different PPy/clay nanocomposites obtained, the images show during polymerization, the clay particles were not visible on the surface of the NCPP nanocomposites. The micrograph shown in Figs. 10 and 11 illustrates a more ordered and denser structure. Smaller aggregates with a high density of the granules are better observed for loading rates of 1%, whereas these aggregates are larger with a lower density per unit area for loading rates of 3.5% (these aggregates are observed by arrows in Figs. 10 and 11). This shows that increasing loading rates in nanocomposites increase the compactness of the samples which become denser. The clay particles have been coated by the polymer (Fig. 10), and can be enhanced by an attractive interaction between the PPy and the surface clay, the polymer is probably bound to the surface by a hydrogen bond between the amine groups of the polymer and the surface oxygen of the clay. The Poly(pyrrole) is in the form of non-uniformly distributed agglomerates, in the case of 10% clay, these organically modified clay particles are more dense (Fig. 11). There are interactions between amines and surface silicates in organophilic Maghnite [38]. The microstructure of a thin layer of polypyrrole is shown in Fig. 11. The film has a uniform granular morphology and the average grain size is approximately 0.5 µm.
3.7 Thermal analysis (DSC)
We observe on the thermogram of the PPy- Mag % nanocomposites the presence of a first endothermic peak located between 105 and 121 °C which indicates the departure of water. A second endothermic peak is located between 250 and 290 °C which is related to the decomposition of the surfactant (CTAB, TBAHS). A third peak is located around 425 °C and 505 °C which is linked to the cross-linking of the polymer chains which is delayed compared to that of polypyrrole, and finally an endothermic peak is located around 507 °C and 549 °C which indicates the decomposition of the nanocomposite. The DSC analysis was performed in order to study the influence of the loading rate on the glass transition temperature of the matrix. According to Fig. 12, the Tg of the PPy/MMT % nanocomposites is higher than that of polypyrrole which is 75.46 °C, this slight increase is due to the introduction of clay into the matrix which makes it more rigid.
4 Conclusion
This work deals with the implementation of PPy/Maghnite-Organophile nanocomposites and the characterization by different analyses (IR, TGA and DRX, SEM, TEM, DSC) which allowed to quantify the quantity of surfactants incorporated in the clay and the spacing between the clay layers. The existance of PPy within the interlayer of clay has been verified by XRD, FTIR, and SEM, TEM studies. Electrical conductivity measurements show a decrease in conductivity with increasing charge rates. The results of thermogravimetric analysis show a significant improvement in the thermal stability of the different nanocomposites developed compared to virgin PPy. Currently, we are investigating the possibility of coating these nanocomposites on coated surfaces for applications in electronic device covers.
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Mrah, L., Meghabar, R. Influence of clay modification process in polypyrrole-layered silicate nanocomposite. SN Appl. Sci. 2, 659 (2020). https://doi.org/10.1007/s42452-020-2338-7
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DOI: https://doi.org/10.1007/s42452-020-2338-7