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Structures of various forms of polyaniline: (a) general form; (b) leucomeraldine; (c) emeraldine; (d) pernigraniline [15].

Structures of various forms of polyaniline: (a) general form; (b) leucomeraldine; (c) emeraldine; (d) pernigraniline [15].

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The wide range of electrical, electrochemical, and optical properties associated with Polyaniline (PANI) and its composites has made them attractive for many industrial applications. In this study, Emeraldine Salt (ES), which is a doped conducting form of PANI, was chemically prepared in situ using the oxidizing agent ammonium persulphate in the pr...

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... is a high molecular weight (typically 100 000) polymer. Its structure can be represented by the general formula shown in Fig. 1a, with n representing the degree of polymerization, and .1 ¡ y/ the oxidation state, varying from 0.0 to 1.0. Thus, leucoemeraldine (Fig. 1b) corresponds to .1 ¡ y/ D 0, emeraldine (Fig. 1c) has .1 ¡ y/ D 0:5. With .1 ¡ y/ D 1:0, we have the completely oxidized state of the polymer, denoted as pernigraniline, a non-conductive form, ...
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... is a high molecular weight (typically 100 000) polymer. Its structure can be represented by the general formula shown in Fig. 1a, with n representing the degree of polymerization, and .1 ¡ y/ the oxidation state, varying from 0.0 to 1.0. Thus, leucoemeraldine (Fig. 1b) corresponds to .1 ¡ y/ D 0, emeraldine (Fig. 1c) has .1 ¡ y/ D 0:5. With .1 ¡ y/ D 1:0, we have the completely oxidized state of the polymer, denoted as pernigraniline, a non-conductive form, shown in Fig. 1d. All of these states, except leucoemeraldine, can be protonated. The states with no protonation are denoted as the 'base' form, ...
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... is a high molecular weight (typically 100 000) polymer. Its structure can be represented by the general formula shown in Fig. 1a, with n representing the degree of polymerization, and .1 ¡ y/ the oxidation state, varying from 0.0 to 1.0. Thus, leucoemeraldine (Fig. 1b) corresponds to .1 ¡ y/ D 0, emeraldine (Fig. 1c) has .1 ¡ y/ D 0:5. With .1 ¡ y/ D 1:0, we have the completely oxidized state of the polymer, denoted as pernigraniline, a non-conductive form, shown in Fig. 1d. All of these states, except leucoemeraldine, can be protonated. The states with no protonation are denoted as the 'base' form, e.g. emeraldine base (which would be ...
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... 1a, with n representing the degree of polymerization, and .1 ¡ y/ the oxidation state, varying from 0.0 to 1.0. Thus, leucoemeraldine (Fig. 1b) corresponds to .1 ¡ y/ D 0, emeraldine (Fig. 1c) has .1 ¡ y/ D 0:5. With .1 ¡ y/ D 1:0, we have the completely oxidized state of the polymer, denoted as pernigraniline, a non-conductive form, shown in Fig. 1d. All of these states, except leucoemeraldine, can be protonated. The states with no protonation are denoted as the 'base' form, e.g. emeraldine base (which would be non-conductive). After protonation, the polymer is denoted as 'salt'. For example, protonation of the emeraldine base form (Fig. 1c) with HCl yields emeraldine ...
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... protonation, the polymer is denoted as 'salt'. For example, protonation of the emeraldine base form (Fig. 1c) with HCl yields emeraldine hydrochoride, as illustrated in Fig. 2 [12][13][14]. ...
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... resulted in electrical conduction even when the volume fraction of ES powder was above 50%. The use of nitrocellulose solution, however, was successful in obtaining electrical conduction with the addition of the ES powder. The experimental data for resistivity versus ller concentration for ES lled nitrocellulose solution are presented in Fig. 11. The resistivity level obtained for the composite lm when it is lled 50% by volume with the ES powder is higher than that for the homogeneous ES powder under 1.3 to 15.8 MPa pressure range (Figs 9, 10, respectively) by about a factor of 2. This difference increases to as high as seventeen-fold when the lm is lled at 30%. This is in ...
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... experimental data for resistivity versus ller concentration for ES lled nitrocellulose solution are presented in Fig. 11. The resistivity level obtained for the composite lm when it is lled 50% by volume with the ES powder is higher than that for the homogeneous ES powder under 1.3 to 15.8 MPa pressure range (Figs 9, 10, respectively) by about a factor of 2. This difference increases to as high as seventeen-fold when the lm is lled at 30%. This is in line with our expectation that, among other characteristics, the resistivity levels of electrically conductive adhesives are largely dependent on the average length of conductive paths between the conductive particles dispersed in the non-conducting matrix [16,18]. ...
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... series of scanning electron micrographs taken at 200£ magni cation shown in Fig. 12 depict the features of the pure ES powder (Fig. 12a), and pure (Fig. 12b) as well as lled nitrocellulose solution (Fig. 12 c -e) adhesive samples fractured subsequent to cure. In Fig. 12a, we see the polydisperse spherical morphology of the bulk ES powder with an average particle diameter of 5-10 ¹m. Figure 12b shows the homogeneous ...
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... series of scanning electron micrographs taken at 200£ magni cation shown in Fig. 12 depict the features of the pure ES powder (Fig. 12a), and pure (Fig. 12b) as well as lled nitrocellulose solution (Fig. 12 c -e) adhesive samples fractured subsequent to cure. In Fig. 12a, we see the polydisperse spherical morphology of the bulk ES powder with an average particle diameter of 5-10 ¹m. Figure 12b shows the homogeneous morphology of the pure nitrocellulose solution after ...
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... series of scanning electron micrographs taken at 200£ magni cation shown in Fig. 12 depict the features of the pure ES powder (Fig. 12a), and pure (Fig. 12b) as well as lled nitrocellulose solution (Fig. 12 c -e) adhesive samples fractured subsequent to cure. In Fig. 12a, we see the polydisperse spherical morphology of the bulk ES powder with an average particle diameter of 5-10 ¹m. Figure 12b shows the homogeneous morphology of the pure nitrocellulose solution after solidii cation by ...
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... series of scanning electron micrographs taken at 200£ magni cation shown in Fig. 12 depict the features of the pure ES powder (Fig. 12a), and pure (Fig. 12b) as well as lled nitrocellulose solution (Fig. 12 c -e) adhesive samples fractured subsequent to cure. In Fig. 12a, we see the polydisperse spherical morphology of the bulk ES powder with an average particle diameter of 5-10 ¹m. Figure 12b shows the homogeneous morphology of the pure nitrocellulose solution after solidii cation by evaporation and fracture after immersion in liquid nitrogen. ...
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... series of scanning electron micrographs taken at 200£ magni cation shown in Fig. 12 depict the features of the pure ES powder (Fig. 12a), and pure (Fig. 12b) as well as lled nitrocellulose solution (Fig. 12 c -e) adhesive samples fractured subsequent to cure. In Fig. 12a, we see the polydisperse spherical morphology of the bulk ES powder with an average particle diameter of 5-10 ¹m. Figure 12b shows the homogeneous morphology of the pure nitrocellulose solution after solidii cation by evaporation and fracture after immersion in liquid nitrogen. Figures 12c, d, and e reveal that the degree of dispersion ...
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... Fig. 12a, we see the polydisperse spherical morphology of the bulk ES powder with an average particle diameter of 5-10 ¹m. Figure 12b shows the homogeneous morphology of the pure nitrocellulose solution after solidii cation by evaporation and fracture after immersion in liquid nitrogen. Figures 12c, d, and e reveal that the degree of dispersion of ES powder in adhesives with different ller loadings is quite different. ...
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... Fig. 12a, we see the polydisperse spherical morphology of the bulk ES powder with an average particle diameter of 5-10 ¹m. Figure 12b shows the homogeneous morphology of the pure nitrocellulose solution after solidii cation by evaporation and fracture after immersion in liquid nitrogen. Figures 12c, d, and e reveal that the degree of dispersion of ES powder in adhesives with different ller loadings is quite different. Both nitrocellulose solutions lled 40% and 50% by volume with ES particles show the llers to be well dispersed within the insulating (Figs 12d, e). ...
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... 12c, d, and e reveal that the degree of dispersion of ES powder in adhesives with different ller loadings is quite different. Both nitrocellulose solutions lled 40% and 50% by volume with ES particles show the llers to be well dispersed within the insulating (Figs 12d, e). On the other hand, a non-uniform dispersion of the llers is observed for the case of 30% concentration (Fig. 12c). ...
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... degree of dispersion of ES powder in adhesives with different ller loadings is quite different. Both nitrocellulose solutions lled 40% and 50% by volume with ES particles show the llers to be well dispersed within the insulating (Figs 12d, e). On the other hand, a non-uniform dispersion of the llers is observed for the case of 30% concentration (Fig. 12c). In order to examine the mechanical and conduction behaviors of the composite adhesive, single lap joints were prepared using ES lled nitrocellulose adhesive on aluminum or zinc (plated), as well as on silver substrates. The experimental results revealed that the adhesive / substrate interphase had a strong in uence on the electrical ...
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... joints with Ag substrates exhibited durable, and continuous conduction property over a period of 30 days ( Table 2). The joint resistivity in these samples (Table 2) fell in the range between those for the homogeneous ES powder under 1.3 to 15.8 MPa pressure range (Figs 9, 10, respectively), and the composite lm values with above 40% volume fraction ES ller (Fig. 11). When aluminum substrates were used, except for one case, all joints became completely non-conductive within 6 days even though the initial resistivity values (Table 3) were not much higher than those for the corresponding composite lm values (Fig. 11). ...
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... Ag substrates exhibited durable, and continuous conduction property over a period of 30 days ( Table 2). The joint resistivity in these samples (Table 2) fell in the range between those for the homogeneous ES powder under 1.3 to 15.8 MPa pressure range (Figs 9, 10, respectively), and the composite lm values with above 40% volume fraction ES ller (Fig. 11). When aluminum substrates were used, except for one case, all joints became completely non-conductive within 6 days even though the initial resistivity values (Table 3) were not much higher than those for the corresponding composite lm values (Fig. 11). In the case of Zn plated substrates, all joints became completely non-conductive ...
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... (Figs 9, 10, respectively), and the composite lm values with above 40% volume fraction ES ller (Fig. 11). When aluminum substrates were used, except for one case, all joints became completely non-conductive within 6 days even though the initial resistivity values (Table 3) were not much higher than those for the corresponding composite lm values (Fig. 11). In the case of Zn plated substrates, all joints became completely non-conductive within one day. This loss of conduction may be attributed to a complex redox-reaction occurring at the boundary between the composite adhesive and the metal substrate. This reaction results in the formation of a dense, non-conduction layer of metallic ...

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