Modification of polyurethane with novel blocking agent

Abstract

Purpose

Fluorinated polyurethane combines some virtues of polyurethane and fluorinated polymer, such as low water absorption, attractive surface properties, good wearability and high weatherability. Fluorocarbon chains have been incorporated into polyurethanes by fluorinated diisocyanates, chain extenders, polyether glycols, polyester glycols and end-cappers. However, the fluorinated polyurethane, which is prepared with monohydric fluorocarbon alcohol, is seldom reported. The purpose of this research is to prepare and apply the novel fluorocarbon alcohols with side chain to modify polyurethane as the blocking agent.

Design/methodology/approach

The novel fluorocarbon alcohol with side chain 2-methoxy-3-nonene perfluorinated oxygen propanol (MNPOP) can be prepared via alcoholysis reaction of methanol and 2,3-epoxypropyl perfluorinated nonene ether (EPPNE), which was prepared with etherification of hexafluoropropene trimer (HFPT) and 2,3-glycidol. Structures of EPPNE and MNPOP are confirmed with FTIR and NMR. The polyurethane can be modified when MNPOP is used as blocking agent.

Findings

In comparison with the conventional polyurethane, the hydrophobic property of fluorinated polyurethane is improved. However, the increase of tensile strength of modified polyurethane is not obvious because MNPOP belongs to monohydric alcohol. And the function of MNPOP in the modified polyurethane is the blocking agent. The thermal stability of conventional and modified polyurethane is almost the same because MNPOP is de-blocked and fluorocarbon chains have not been incorporated into polyurethanes when the temperature is more than 150°C.

Originality/value

The polyurethane is modified with the novel fluorocarbon alcohols with side chain, which functions as the blocking agent. The hydrophobic property of fluorinated polyurethane is improved.

Citation

Chen, L. and Jiang, W. (2014), "Modification of polyurethane with novel blocking agent", Pigment & Resin Technology, Vol. 43 No. 2, pp. 97-103. https://doi.org/10.1108/PRT-04-2013-0030