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PANI polyaniline

Polyaniline (PANI) is one of the most frequently investigated conducting polymers because of its ease of synthesis, its relative environmental stabUity and its abUity to exist in a range of intrinsic redox states. PANI exists in various oxidation states, ranging Irom a reduced leucoemeraldine form to the fully oxidized pemigraniline form. [Pg.168]

Other studies in 2000 by Drew et al. reported that it is very difficult to spin fibers of PANI complexed to sulfonated polystyrene (PANFSPS), even when solutions containing sodium chloride and dodecyl benzene sulfonic acid sodium salt were used to lower the surface tension and thereby enhance electrospinning [16,17]. However, PANFSPS nanofibers can be produced by adding a carrier polymer such as PEO, polyacrylonitrile, or polyurethane. Also reported was the use of electrostatically layered sulfonated polystyrene as a template for the surface polymerization of conjugated polymers in their conducting form. Enzymatic synthesis of PANI and a copolymer of pyrrole and PEDOT was done on electrospun nanofiber [Pg.169]

Another study by Hong et al. also reports the preparation of conducting PANI/nylon-6 composites with high electrical conductivity and superior mechanical properties, such as flexibility and lightness [24]. PANI was chemically polymerized on the surface of the nylon-6 electrospun nanofiber webs. The electrical conductivity measurements showed that the conductivity of the PANI/nylon-6 composite electrospun fiber webs was superior to that of PANI/nylon-6 plain-weave fabrics because of the high surface area/volume ratios. The volume conductivities of the PANI/nylon-6 composite electrospun fiber webs increased from 0.5 to 1.5 S cm as the di sion time increased from 10 min to 4h because of the even distribution of PANI in the electrospun fiber webs. However, the surface conductivities of the PANI/nylon-6 composite electrospun fiber webs somewhat decreased from 0.22 to 0.14 S cm as the di sion time increased, probably because PANI was contaminated with aniline monomers, aniline oligomers, and some alkyl chains, which served as electrical resistants. [Pg.171]


Polyaniline (PANI) can be formed by electrochemical oxidation of aniline in aqueous acid, or by polymerization of aniline using an aqueous solution of ammonium thiosulfate and hydrochloric acid. This polymer is finding increasing use as a "transparent electrode" in semiconducting devices. To improve processibiHty, a large number of substituted polyanilines have been prepared. The sulfonated form of PANI is water soluble, and can be prepared by treatment of PANI with fuming sulfuric acid (31). A variety of other soluble substituted AJ-alkylsulfonic acid self-doped derivatives have been synthesized that possess moderate conductivity and allow facile preparation of spincoated thin films (32). [Pg.242]

Polyanilines. Initial preparations of polyaniline (PANI) led to insoluble materials that were difficult to characterize. Use of model compounds and polymers (124,125) allowed for definitive stmctural analysis. Poly( phenylene amineimine) (PPAI) was synthesized directiy to demonstrate that PANI is purely para-linked (126). The synthesis was designed so as to allow linkage through the nitrogen atoms only (eq. 9). Comparison of the properties of PPAI and PANI showed PPAI to be an excellent model both stmcturaHy and electronically. [Pg.38]

A thin layer deposited between the electrode and the charge transport material can be used to modify the injection process. Some of these arc (relatively poor) conductors and should be viewed as electrode materials in their own right, for example the polymers polyaniline (PAni) [81-83] and polyethylenedioxythiophene (PEDT or PEDOT) [83, 841 heavily doped with anions to be intrinsically conducting. They have work functions of approximately 5.0 cV [75] and therefore are used as anode materials, typically on top of 1TO, which is present to provide lateral conductivity. Thin layers of transition metal oxide on ITO have also been shown [74J to have better injection properties than ITO itself. Again these materials (oxides of ruthenium, molybdenum or vanadium) have high work functions, but because of their low conductivity cannot be used alone as the electrode. [Pg.537]

Electrochemical measurements on polyaniline (PANI) produce a picture of the charge storage mechanism of conducting polymers which differs fundamentally from that obtained using PTh or PPy. In the cyclic voltammetric experiment one observes at least two reversible waves in the potential range between —0.2 and -)-1.23 V vs SCE. Above -1-1.0 V the charging current tends to zero. Capacitive currents and overoxidation effects, as with PPy and PTh, do not occur The striking... [Pg.28]

Other materials which appear to be suitable as active battery el trodes are polyazulene poly (A-vinylcarbazole) polyquinolines and, most recently, polyaniline (PANI) panI, in particular, is a promising material for the... [Pg.32]

Another convenient way to disperse platinum-based electrocatalysts is to use electron-conducting polymers, such as polyaniline (PAni) or polypyrrole (PPy), which play the role of a three-dimensional electrode.In such a way very dispersed electrocatalysts are obtained, with particle sizes on the order of a few nanometers, leading to a very high activity for the oxidation of methanol (Fig. 10). [Pg.86]

PP-g-MA) silicate nanocomposites and intercalated thermoset silicate nanocomposites for flame-retardant applications were characterised by XRD and TEM [333], XRD, TEM and FTIR were also used in the study of ID CdS nanoparticle-poly(vinyl acetate) nanorod composites prepared by hydrothermal polymerisation and simultaneous sulfidation [334], The CdS nanoparticles were well dispersed in the polymer nanorods. The intercalation of polyaniline (PANI)-DDBSA (dodecylbenzene-sulfonate) into the galleries of organo-montmorillonite (MMT) was confirmed by XRD, and significantly large 4-spacing expansions (13.3-29.6A) were observed for the nanocomposites [335],... [Pg.647]

Electronically conducting polymers (ECPs) such as polyaniline (PANI), polypyrrole (PPy) and po 1 y(3.4-cthy 1 cncdi oxyth iophcnc) (PEDOT) have been applied in supercapacitors, due to their excellent electrochemical properties and lower cost than other ECPs. We demonstrated that multi-walled carbon nanotubes (CNTs) prepared by catalytic decomposition of acetylene in a solid solution are very effective conductivity additives in composite materials based on ECPs. In this paper, we show that a successful application of ECPs in supercapacitor technologies could be possible only in an asymmetric configuration, i.e. with electrodes of different nature. [Pg.64]

The mechanisms and reasons of catalytic activity of polyaniline (PANI)-type conducting polymers toward oxygen reduction in acidic and saline solutions are investigated by electrochemical and quantum-chemical methods. The PANI/thermally expanded graphite compositions were developed for realization of fully functional air gas-diffusion electrodes. Principally new concept for creation of rechargeable metal-air batteries with such type of catalysts is proposed. The mockups of primary and rechargeable metal-air batteries with new type of polymer composite catalysts were developed and tested. [Pg.110]

Polyaniline (PANI) was investigated as electrocatalyst for the oxygen reduction reaction in the acidic and neutral solutions. Galvanostatic discharge tests and cyclic voltammetry of catalytic electrodes based on polyaniline in oxygen-saturated electrolytes indicate that polyaniline catalyzes two-electron reduction of molecular oxygen to H2O2 and HO2". [Pg.124]

For example, the investigations of the current-generating mechanism for the polyaniline (PANI) electrode have shown that at least within the main range of potential AEn the "capacitor" model of ion electrosorption/ desorption in well conducting emeraldine salt phase is more preferable. Nevertheless, the possibilities of redox processes at the limits and beyond this range of potentials AEn should be taken into account. At the same time, these processes can lead to the fast formation of thin insulation passive layers of new poorly conducting phases (leucoemeraldine salt, leucoemeraldine base, etc.) near the current collector (Figure 7). The formation of such phases even in small amounts rapidly inhibits and discontinues the electrochemical process. [Pg.319]

Zengin et al. [41] characterized a polyaniline (PANI)/MWNT composite. The FTIR spectra of the composite film show benzoid and quinoid ring vibrations at 1500cm-1 and 1600 cm-1, respectively, which indicate the presence of emeraldine salt (ES) of polyaniline. A weak broad band near 3400 cm-1 is assigned to the N—H stretching mode. The strong band at 1150cm-1 is characteristic of PANI conductivity. The FTIR spectrum of PANI/MWNT composite in the ES form exhibits several clear differences from the spectrum of neat ES PANI (1) the composite spectrum shows an inverse... [Pg.515]

Polyaniline (PAni, PANI), 73 550 22 207t. See also PAni/V205 entries applications, 7 538... [Pg.724]

The use of conjugated polymer as membranes to separate various liquid mixtures has been reported in the literature [19,20], From those, polyaniline (PANi) is one of the most interesting and studied conjugated polymers. Polyaniline is usually prepared by direct oxidative polymerization of aniline in the presence of a chemical oxidant, or by electrochemical polymerization on different electrode materials [21,22], The possible interconversions between different oxidation states and protonated and depronated states [23], figure 4, make this material remarkable for different purposes. Under most conditions, PANi... [Pg.124]

The use of pyrolyzed polyacrylonitrile (PPAN) and polyaniline (PAni) (Fig. 15.8(d), (e)) as catalysts for the ODH of ethylbenzene should only be mentioned here for the sake of completeness. Although first results were quite promising [45], this concept has so far not been followed in terms of N-doped nanocarbon catalyst development. This is most likely due to the poor self-oxidation resistance as a result of polar C-N bonds. [Pg.403]

Fig. 1 Building units of conducting polymers, (1) polyacetylene (PA) (2) polypyrrole (PPy), polythiophene (PTh), polyfurane (PFu) (3) polyphenylene (PP) (4) polyaniline (PANI) 5 polyindole (PIND) (6) polycarbazole (PCaz) (7) polyazulene (Paz) (8) polynaphthalene (PNa) (9) polyanthracene (PAnth) (10) polypyrene (PPyr) (11) polyfluorene (PFiu) (12) poly(isothionaphthalene) (PITN) (13) poly(dithienothiophene) (14) poly(thienopyrrole) (15) poly(dithienylbenzene) (1G) poly(3-alkylthiophene) (17) poly(phenylene vinylene) (18) poly(bipyrrole) (PBPy), poly(bithiophene) (PBT) (19) poly(phenylenesulfide) (20) 4-poly(thienothiophene) (21) poly(thienyl vinylene), poly(furane vinylene) (22) poly(ethylenedioxythiophene) (PEDOT). Fig. 1 Building units of conducting polymers, (1) polyacetylene (PA) (2) polypyrrole (PPy), polythiophene (PTh), polyfurane (PFu) (3) polyphenylene (PP) (4) polyaniline (PANI) 5 polyindole (PIND) (6) polycarbazole (PCaz) (7) polyazulene (Paz) (8) polynaphthalene (PNa) (9) polyanthracene (PAnth) (10) polypyrene (PPyr) (11) polyfluorene (PFiu) (12) poly(isothionaphthalene) (PITN) (13) poly(dithienothiophene) (14) poly(thienopyrrole) (15) poly(dithienylbenzene) (1G) poly(3-alkylthiophene) (17) poly(phenylene vinylene) (18) poly(bipyrrole) (PBPy), poly(bithiophene) (PBT) (19) poly(phenylenesulfide) (20) 4-poly(thienothiophene) (21) poly(thienyl vinylene), poly(furane vinylene) (22) poly(ethylenedioxythiophene) (PEDOT).
To use polyaniline (PANI) as indicator electrode in the titration of trimeprazine base with tartaric acid in isopropanol solution. [Pg.997]

New materials Polyaniline (PANI) shows high temperature H binding... [Pg.17]


See other pages where PANI polyaniline is mentioned: [Pg.44]    [Pg.97]    [Pg.416]    [Pg.111]    [Pg.305]    [Pg.351]    [Pg.3]    [Pg.59]    [Pg.568]    [Pg.125]    [Pg.202]    [Pg.135]    [Pg.370]    [Pg.607]    [Pg.122]    [Pg.135]    [Pg.1020]    [Pg.125]    [Pg.1020]    [Pg.239]    [Pg.44]    [Pg.106]    [Pg.108]    [Pg.547]    [Pg.299]    [Pg.658]   


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