2009
DOI: 10.1002/kin.20411
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A study on the kinetics of condensation reaction of cardanol and formaldehyde, part I

Abstract: Novolac resins having cardanol-to-formaldehyde mole ratios of 1:0.4, 1:0.5, and 1:0.6 were prepared by using aromatic sulphonic acid as the catalyst at four different temperatures ranging between 90 • C and 120 • C, with an interval of 10 • C. Free formaldehyde and free phenol contents were determined at regular time intervals to check the completion of the reaction. The synthesized novolacs were characterized by Fourier-transform infrared spectroscopic analysis, nuclear magnetic resonance, and gel permeation … Show more

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Cited by 15 publications
(7 citation statements)
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“…Resins derived from CNSL/cardanol are widely employed in the field of surface coatings, adhesives, laminates, rubber compounding and have several miscellaneous applications. Cardanol, like phenol, can be condensed with active hydrogen containing compounds such as formaldehyde to yield a series of phenolic resins, for instance, base-catalyzed resoles and acid-catalyzed novolacs [1][2][3][4][5][6][7][8][9]. The cardanol-based novolac-type phenolic resins may be modified to develop epoxy resins with epichlorohydrin to enhance the performance of such resins in various fields [10][11][12][13].…”
Section: Introductionmentioning
confidence: 99%
“…Resins derived from CNSL/cardanol are widely employed in the field of surface coatings, adhesives, laminates, rubber compounding and have several miscellaneous applications. Cardanol, like phenol, can be condensed with active hydrogen containing compounds such as formaldehyde to yield a series of phenolic resins, for instance, base-catalyzed resoles and acid-catalyzed novolacs [1][2][3][4][5][6][7][8][9]. The cardanol-based novolac-type phenolic resins may be modified to develop epoxy resins with epichlorohydrin to enhance the performance of such resins in various fields [10][11][12][13].…”
Section: Introductionmentioning
confidence: 99%
“…Several publications from Sultania et al are related to the synthesis of VE resins from cardanol . First, a cardanol‐based novolac precursor was synthesized from cardanol and formaldehyde . Then, the epoxidation of the cardanol‐based novolac precursor is conducted with epichlorhydrin .…”
Section: Introductionmentioning
confidence: 99%
“…An irreversible non-spontaneous second-order reaction using cardanol with formaldehyde in the presence of organic weak acids such as p-toluenesulfonic acid, ethanedioic acid, amber acid and citiricacid acid as the catalyst was carried out [59][60][61]. In all the systems, the value of step rate constant k1 were found to be lower than k2, thus the condensation reaction may be considered as the rate-determining stage of the whole reaction.…”
Section: Cardanol Based Phenolic Resinmentioning
confidence: 99%