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3859222 
Journal Article 
Grafting of perfluoroalkyl chains onto wood using blocked isocyanates 
Engonga, PE; Marchetti, V; Gerardin, P; Tekely, P; Loubinoux, B 
2000 
Yes 
Journal of Fluorine Chemistry
ISSN: 0022-1139
EISSN: 1873-3328 
Elsevier 
101 
19-25 
English 
Chemical modification of wood was investigated using blocked isocyanates prepared from reaction of 4,4'-diphenylmethane diisocyanate (MDI) with I equivalent of 2-perfluorohexyl ethanol followed by addition of 1.1 equivalent of methyl ethyl ketoxime (MEKO). Thermal dissociation of the urethane linkage bearing a methyl ethyl ketoxime group allows generation of free isocyanate which reacts with alcohols like cyclohexanol or benzyl alcohol. The reaction was then extended to the hydroxyl groups of wood in order to bind perfluoroalkyl chains. Reaction was first studied on wood meal before grafting on blocks. Such modified blocks possess improved dimensional stability compared to untreated ones. Contact angle measurements were also performed. sigma values obtained for modified blocks were greater and did not decrease with time compared to those obtained with unmodified blocks. (C) 2000 Elsevier Science S.A. All rights reserved. 
contact angle; perfluoroalkyl; blacked isocyanates; anti-swelling-efficiency; dimensional stabilization; wood 
PFAS
• FtOH 6:2
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          Excluded/Not on Topic
• ^Per- and Polyfluoroalkyl Substances (PFAS)
     FtOH 6:2 (647-42-7)
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