TY - JOUR
T1 - Aniline and oligoaniline modified cyclohexanone-formaldehyde resins
AU - Ateş, E.
AU - Kizilcan, N.
PY - 2011
Y1 - 2011
N2 - Purpose - Cyclohexanone-formaldehyde resins (CF-Rs) were ITin situ/IT modified with aniline, 4-aminodiphenylamine, and ITN/IT-ITN/IT'-diphenyl-1,4- phenylene diamine in presence of sodium hydroxide. The purpose of this paper is to report the synthesis of conducting resins with aniline, dimer and trimer aniline, with a one-step method of ITin situ/IT modification of ketonic resin. The roles of ketone, aniline concentration, the conductivity of the product are investigated. Design/methodology/approach - Ketone, formalin (37 per cent aqueous solution), aniline or oligoaniline were mixed and 20 per cent aqueous NaOH solution was added to produce the resin. Findings - The aniline-modified (CF-Rs) were found to have conductivity values of 10UP-3/UP-10UP-5/UP S/cm and may be considered as conductive ketonic resin. Research limitations/implications - The reaction mixture must be stirred continuously. Amount of aniline and oligoaniline is limited. Subsequently, 37 per cent formalin was added dropwise in total while refluxing. The amount of aniline is limited since the formed resin may become insoluble in common organic solvents. Practical implications - This work provides the application of conducting resins. The modified resins containing aniline groups may also promote the adhesive strength of a coating and corrosion inhibition to metal surfaces. Originality/value - Aniline formaldehyde, ITN/IT-ITN/IT'-diphenyl-1,4-phenylenediamine-formaldehyde, aniline- and oligoaniline-modified (CF-Rs) have been synthesised in the presence of a base catalyst. These resins are conductive resins and the ketonic resins formed have physical properties of both aniline-formaldehyde resins such as conductivity.
AB - Purpose - Cyclohexanone-formaldehyde resins (CF-Rs) were ITin situ/IT modified with aniline, 4-aminodiphenylamine, and ITN/IT-ITN/IT'-diphenyl-1,4- phenylene diamine in presence of sodium hydroxide. The purpose of this paper is to report the synthesis of conducting resins with aniline, dimer and trimer aniline, with a one-step method of ITin situ/IT modification of ketonic resin. The roles of ketone, aniline concentration, the conductivity of the product are investigated. Design/methodology/approach - Ketone, formalin (37 per cent aqueous solution), aniline or oligoaniline were mixed and 20 per cent aqueous NaOH solution was added to produce the resin. Findings - The aniline-modified (CF-Rs) were found to have conductivity values of 10UP-3/UP-10UP-5/UP S/cm and may be considered as conductive ketonic resin. Research limitations/implications - The reaction mixture must be stirred continuously. Amount of aniline and oligoaniline is limited. Subsequently, 37 per cent formalin was added dropwise in total while refluxing. The amount of aniline is limited since the formed resin may become insoluble in common organic solvents. Practical implications - This work provides the application of conducting resins. The modified resins containing aniline groups may also promote the adhesive strength of a coating and corrosion inhibition to metal surfaces. Originality/value - Aniline formaldehyde, ITN/IT-ITN/IT'-diphenyl-1,4-phenylenediamine-formaldehyde, aniline- and oligoaniline-modified (CF-Rs) have been synthesised in the presence of a base catalyst. These resins are conductive resins and the ketonic resins formed have physical properties of both aniline-formaldehyde resins such as conductivity.
KW - Coatings
KW - Epoxy resins
KW - Resins
KW - Surface conductivity
UR - http://www.scopus.com/inward/record.url?scp=79251624145&partnerID=8YFLogxK
U2 - 10.1108/03699421111095919
DO - 10.1108/03699421111095919
M3 - Article
AN - SCOPUS:79251624145
SN - 0369-9420
VL - 40
SP - 29
EP - 35
JO - Pigment and Resin Technology
JF - Pigment and Resin Technology
IS - 1
ER -