2002
DOI: 10.1016/s0032-3861(02)00062-9
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Synthesis and curing behaviors of a crosslinkable polymer from cashew nut shell liquid

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Cited by 90 publications
(61 citation statements)
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“…This could be due to the extra or synergistic contribution of others CNSL components besides cardanol (cardol, 2-methyl-cardol and polymerized material). 3,4 Cardol is known to contribute more towards the antioxidant activity of CNSL than cardanol. 13 One important parameter in the antioxidant activity is the molar mass.…”
Section: Effect Of Cnsl Derivative Structurementioning
confidence: 99%
See 1 more Smart Citation
“…This could be due to the extra or synergistic contribution of others CNSL components besides cardanol (cardol, 2-methyl-cardol and polymerized material). 3,4 Cardol is known to contribute more towards the antioxidant activity of CNSL than cardanol. 13 One important parameter in the antioxidant activity is the molar mass.…”
Section: Effect Of Cnsl Derivative Structurementioning
confidence: 99%
“…3 Depending on the conditions of the roasting process, the composition of the technical CNSL can change and reach higher cardanol content (83-84%), less cardol (8-11%) and maintain polymeric material as 10% and 2-methyl cardol content as 2%. 4 The use of natural antioxidants is well established. Hindered phenolic compounds (ArOH) represent the major family of both natural and synthetic antioxidants.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, its composition varies as it depends on the time and temperature to which the cashew was submitted. Normally the composition of the technical CNSL is: 60 to 95% cardanol, 4 to 19% cardol, 1 to 2% of anacardic acid, 0.3 to 10% of polymeric material and 1.2 to 4.1% of 2-methylcardol [4,16,17] . The CNSL obtained with super critical CO 2 presented cardanol as its main component (75 to 88%), with its concentration depending on the operational parameters.…”
Section: Introductionmentioning
confidence: 99%
“…The phenolic nature of the material makes it possible to react under a variety of conditions to form both base catalyzed resoles and acid catalyzed novolacs [6] . Cardanol is a source of unsaturated hydrocarbon phenol and behaves as an excellent monomer for thermosetting polymer production [7,8] . Cardanol Formaldehyde is synthesized from CNSL (Cashew Nut Shell Liquid) either by polycondensation with electrophilic compounds, such as formaldehyde, furfuraldehyde or by chain polymerization through the unsaturation presents in the side chain using acid catalysts or by the functionalization at the hydroxyl group and subsequent oligomerization to obtain a functionalized pre-polymer.…”
Section: Introductionmentioning
confidence: 99%