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Photo: Barnabà<br />

Materials<br />

CTS offers a series of products based on the phenolic structure derived<br />

from cashew nut shells.<br />

• Cardanol-based phenolic resins (novolacs) as curing agents of<br />

commercial epoxy resins;<br />

• Cardanol-based polyols (POLYCARD XFN) for the preparation of<br />

polyurethanes;<br />

• Cardanol-based epoxy-novolacs (NOVOCARD XFN);<br />

• Saturated and unsaturated polyester resins prepared using cardanol<br />

derivatives;<br />

• Cardanol-based aminoalcohols to be used in polymeric matrices with<br />

a polyurea scaffold;<br />

• Cardanol-based acrylic and methacrylic monomers as additives for<br />

coating or varnishes;<br />

• Cardanol-based benzoxazines as either coupling agents for glass and<br />

natural fibres or as reticulating agents for epoxy resins.<br />

Cardanol based polyols for poluyrethanes<br />

Polycard XFN product line is a family of earth-friendly polyols derived<br />

from cardanol for the formulation of both high and low density rigid<br />

polyurethane foams, flexible polyurethane foams for use in insulating<br />

foams, mattresses and couches, elastomers and coatings. The high<br />

percentage of primary hydroxyl groups give these polyols a relatively<br />

high rate of reactivity with isocyanates. In addition to classic polyols an<br />

aminolachol monomer, AMINOLCARD XFN-AM120, is available.<br />

Cardanol based epoxy hardeners<br />

Novocard XFN products are liquid cardanol/formaldehyde novolacs<br />

designed to be used as curing agent in formulating heat cured bisphenol-<br />

A and bisphenol-F epoxy resins. Their long alkenyl side chains impart<br />

flexibility in cured epoxy resins. The intrinsic properties of the phenolic<br />

structure are chemical resistance, heat and flame resistance. Novocard<br />

XFN can also be used as polyols for polyurethane formulations.<br />

Cardanol based epoxy monomer and resins<br />

Epocard XFN are epoxy monomers and resins suitable for composite<br />

manufacture and coating applications which are available in a wide range<br />

of viscosities. The alkyl side chain of the phenolic ring enhances the<br />

final product flexibility, while the phenolic structure enhances chemical<br />

resistance, heat and flame durability. Epoxy Equivalent Weight and their<br />

formulation can be tailored for any end-use. - MT<br />

References:<br />

CTS-Materials Divison Brochure<br />

wikipedia<br />

Tullo, Alexander H.: (September 8,<br />

2008). „A Nutty Chemical“. Chemical and<br />

Engineering News 86 (36): 26–27.<br />

Senning, Alexander: (2006). Elsevier‘s<br />

Dictionary of Chemoetymology. Elsevier.<br />

ISBN 0444522395<br />

Ikeda, Ryohei et. al.: (2000). „A new<br />

crosslinkable polyphenol from a<br />

renewable resource“. Macromolecular<br />

Rapid Communications 21 (8): 496–499.<br />

www.ctsusa.us<br />

bioplastics MAGAZINE [05/09] Vol. 4 29

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