## Abstract Phenol‐modified cardanol–formaldehyde novolac resins have been synthesized using equal proportions of phenol and cardanol. To this mixture of phenol and cardanol, 0.6 and 0.8 mol of formaldehyde were added separately, under acidic conditions, at five different temperatures ranging betwe
A study on the kinetics of condensation reaction of cardanol and formaldehyde, part I
✍ Scribed by Minakshi Sultania; J. S. P. Rai; Deepak Srivastava
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 290 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
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 chromatography. The reaction between cardanol and formaldehyde was found to follow second‐order kinetics. The overall rate constant (k) increased with the increase of temperature. On the basis of the value of k, various other activation parameters such as activation energy (E~a~), change in enthalpy (ΔH), entropy (ΔS), and free energy (ΔG) of the reaction were also evaluated. It was found that the condensation reaction of cardanol and formaldehyde with aromatic sulphonic acid was nonspontaneous and irreversible. © 2009 Wiley Periodicals, Inc. Int J Chem Kinet 41: 559–572, 2009
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In the present study, a quick method for the determination of composition of the resin formed by alkaline-catalyzed cardanol-formaldehyde reaction has been suggested. The complete analysis of the product could be carried out by determining experimentally the concentration of only one reactant, viz.,