1999
DOI: 10.1016/s0379-6779(98)01166-7
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Sulfonated polyaniline

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Cited by 29 publications
(20 citation statements)
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“…[14,15] A similar decrease in the conductivity was observed for AN/(3-aminobenzene sulfonic acid) copolymers. [29] As illustrated in Figures 7-9, the conductivity of the AN/ SDP (50:50) copolymers steadily increases with an increase in the oxidant/monomer ratio, monomer concentration, or by extending the polymerization time, because of an increase in the oxidized-state content or molecular weight and therefore conjugation length. However, the conductivity of the copolymers varies unusually with HCl concentration (Figure 10) and polymerization temperature (data not shown).…”
Section: Properties Of the An/sdp Copolymer Particlesmentioning
confidence: 93%
“…[14,15] A similar decrease in the conductivity was observed for AN/(3-aminobenzene sulfonic acid) copolymers. [29] As illustrated in Figures 7-9, the conductivity of the AN/ SDP (50:50) copolymers steadily increases with an increase in the oxidant/monomer ratio, monomer concentration, or by extending the polymerization time, because of an increase in the oxidized-state content or molecular weight and therefore conjugation length. However, the conductivity of the copolymers varies unusually with HCl concentration (Figure 10) and polymerization temperature (data not shown).…”
Section: Properties Of the An/sdp Copolymer Particlesmentioning
confidence: 93%
“…All doped forms of PANI (conductive) are practically insoluble substances. However, dissolution of the doped PANI in NMP can be achieved adding a small amount of TEA [14] or another amine, e.g. diethylamine, ethylenediamine.…”
Section: Resultsmentioning
confidence: 99%
“…The subsequent polymerization of ANIA is therefore inhibited, which leads to a large portion of unreacted ANIA even at longer reaction times, as can be seen in Fig 3 and in Table 1. Thus, only a small part of ANIA participates in copolymerization, which suggests that ANIA alone hardly generates the reactive intermediates, which is due to the unfavorable combination of electron‐withdrawing and steric effects of the sulfonic16, 18, 19 or carboxylic group. This is supported also by the composition of OMA and MA copolymers prepared in a bench‐scale synthesis 18.…”
Section: Resultsmentioning
confidence: 99%