2007
DOI: 10.1002/app.26628
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Modification of high ortho novolac resin with diacids to improve its mechanical properties

Abstract: To improve the brittleness of high ortho novolac resins, at first, high ortho novolac resins (N) were synthesized and condensation reactions between N and flexible diacids such as adipic acid (DA4) and azelaic acid (DA7) were carried out with different amounts of diacids, in the presence of zinc acetate as catalyst, in toluene as solvent. To characterize the diacid-modified resins (MN), FT-IR analysis, TGA and DSC techniques were used. The morphologies of MN were also investigated. Moldings were prepared from … Show more

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Cited by 12 publications
(5 citation statements)
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“…0.5 mole phenol, 1.5 mole formaldehyde and NaOH as a catalyst were added to a glass polymerization flask and the temperature of the system was kept constant at 65°C in water bath. The reaction was followed by the determination of the free formaldehyde amount according to the hydroxylamine hydrochloride method (Iyim, 2007). After the reaction, PF resin was purified (excess phenol and water were removed) under vacuum in a rotary evaporator system.…”
Section: Methodsmentioning
confidence: 99%
“…0.5 mole phenol, 1.5 mole formaldehyde and NaOH as a catalyst were added to a glass polymerization flask and the temperature of the system was kept constant at 65°C in water bath. The reaction was followed by the determination of the free formaldehyde amount according to the hydroxylamine hydrochloride method (Iyim, 2007). After the reaction, PF resin was purified (excess phenol and water were removed) under vacuum in a rotary evaporator system.…”
Section: Methodsmentioning
confidence: 99%
“…Despite the centenary, the phenolic resins are still used for a range of applications, such as thermal insulation materials, adhesives, powders of molding, laminated resins, coating of surfaces, and composites [14,15]. This occurs because of its excellent properties like dimensional stability, chemical resistance, thermal stability, and its role as a flame retardant [15][16][17].…”
Section: Introductionmentioning
confidence: 98%
“…The mechanism of chemical modification is to introduce long and flexible molecular chains into the rigid backbone of phenolic resin to improve its toughness, and the large amounts of reactive hydroxymethyl and hydroxyl groups in phenolic resin, which can react with toughening materials, provide the foundation of chemical modification . For example, many polymers with flexible molecular chains and active groups like dicarboxylic acid, epoxy resin, PU prepolymer, cardanol, and polyethylene glycol (PEG) can be used to toughen the resin. Unfortunately, the chemical modification using these flammable polymers always sacrifices the excellent fire‐retardant performance of phenolics.…”
Section: Introductionmentioning
confidence: 99%