186
Clement, K.S., Walker, L.L., Wehmeyer, R.M., Whitmarsh, R.H., Molzahn, D.C., Dianis, W.P.,
& Laycock, D.E. (2002). Polymerization of ethylene oxide using metal cyanide catalysts. US
Patent 6,429,342. Available in: https://patents.google.com/patent/us6429342b1/en
Clemitson, I. R. (Ed.). (2015). Castable polyurethane elastomers. CRC Press. ISBN
9781138809208.
Corcuera, M. A., Rueda, L., Saralegui, A., Martín, M. D., Fernández-d’Arlas, B., Mondragon, I.,
& Eceiza, A. (2011). Effect of diisocyanate structure on the properties and microstructure of
polyurethanes based on polyols derived from renewable resources. Journal of Applied Polymer
Science, 122(6), 3677–3685. https://doi.org/10.1002/app.34781.
Cousinet, S., Ghadban, A., Fleury, E., Lortie, F., Pascault, J.-P., & Portinha, D. (2015). Toward
replacement of styrene by bio-based methacrylates in unsaturated polyester resins. European
Polymer Journal, 67, 539–550. https://doi.org/10.1016/j.eurpolymj.2015.02.016.
Crapper, G. (2012). Powder coatings.
Crawford, D. M., Bass, R. G., & Haas, T. W. (1998). Strain effects on thermal transitions and
mechanical properties of thermoplastic polyurethane elastomers. Thermochimica Acta,
323(1–2), 53–63. https://doi.org/10.1016/s0040-6031(98)00541-3.
Dai, J., Ma, S., Liu, X., Han, L., Wu, Y., Dai, X., & Zhu, J. (2015). Synthesis of bio-based unsaturated polyester resins and their application in waterborne UV-curable coatings. Progress in
Organic Coatings, 78, 49–54. https://doi.org/10.1016/j.porgcoat.2014.10.007.
Datta, J., Kosiorek, P., & Włoch, M. (2017). Synthesis, structure and properties of poly(etherurethane)s synthesized using a tri-functional oxypropylated glycerol as a polyol.
Journal of Thermal Analysis and Calorimetry, 128(1), 155–167. https://doi.org/10.1007/
s10973-016-5928-2.
De Hoe, G. X., Zumstein, M. T., Tiegs, B. J., Brutman, J. P., McNeill, K., Sander, M., Coates,
G. W., & Hillmyer, M. A. (2018). Sustainable polyester elastomers from lactones: Synthesis,
properties, and enzymatic hydrolyzability. Journal of the American Chemical Society, 140(3),
963–973. https://doi.org/10.1021/jacs.7b10173.
Delebecq, E., Pascault, J.-P., Boutevin, B., & Ganachaud, F. (2012). On the versatility of urethane/
urea bonds: Reversibility, blocked isocyanate, and non-isocyanate polyurethane. Chemical
Reviews, 113(1), 80–118. https://doi.org/10.1021/cr300195n.
Deligny, P., & Tuck, N. (2000). Alkyds & polyesters. Wiley.
Díaz, A., Katsarava, R., & Puiggalí, J. (2014). Synthesis, properties and applications of biodegradable polymers derived from diols and dicarboxylic acids: From polyesters to poly(ester amide)
s. International Journal of Molecular Sciences, 15(5), 7064–7123. https://doi.org/10.3390/
ijms15057064.
Ding, H., Wang, J., Liu, J., Xu, Y., Chen, R., Wang, C., & Chu, F. (2015). Preparation and properties of a novel flame retardant polyurethane quasi-prepolymer for toughening phenolic foam.
Journal of Applied Polymer Science, 132(35). https://doi.org/10.1002/app.42424.
Dodiuk, H., & Goodman, S. H. (Eds.). (2013). Handbook of thermoset plastics (3rd ed. Edition.
ISBN 978-1-4557-3107-7). William Andrew. https://doi.org/10.1016/c2011-0-09694-1.
Domschke, A., Lohmann, D., & Hopken, J. (2000). Polysiloxane-polyol macromers, their preparation and their use. U.S. Patent No. 6,043,328. Washington, DC: U.S. Patent and Trademark
Office. Available in: https://patents.google.com/patent/us6043328a/en
Dušek, K., Špírková, M., & Ilavský, M. (1991). Network formation in polyurethanes due to
allophanate and biuret formation: Gel fraction and equilibrium modulus. Macromolecular
Symposia, 45(1), 87–95. https://doi.org/10.1002/masy.19910450112.
Dutta, N., Karak, N., & Dolui, S. (2004). Synthesis and characterization of polyester resins based
on nahar seed oil. Progress in Organic Coatings, 49(2), 146–152. https://doi.org/10.1016/j.
porgcoat.2003.09.005.
Dyer, E., Taylor, H. A., Mason, S. J., & Samson, J. (1949). The rates of reaction of isocyanates with
alcohols. I. Phenyl isocyanate with 1-and 2-butanol. Journal of the American Chemical Society,
71(12), 4106–4109. https://doi.org/10.1021/ja01180a064.
M. Akbari and R. Najjar
Clement, K.S., Walker, L.L., Wehmeyer, R.M., Whitmarsh, R.H., Molzahn, D.C., Dianis, W.P.,
& Laycock, D.E. (2002). Polymerization of ethylene oxide using metal cyanide catalysts. US
Patent 6,429,342. Available in: https://patents.google.com/patent/us6429342b1/en
Clemitson, I. R. (Ed.). (2015). Castable polyurethane elastomers. CRC Press. ISBN
9781138809208.
Corcuera, M. A., Rueda, L., Saralegui, A., Martín, M. D., Fernández-d’Arlas, B., Mondragon, I.,
& Eceiza, A. (2011). Effect of diisocyanate structure on the properties and microstructure of
polyurethanes based on polyols derived from renewable resources. Journal of Applied Polymer
Science, 122(6), 3677–3685. https://doi.org/10.1002/app.34781.
Cousinet, S., Ghadban, A., Fleury, E., Lortie, F., Pascault, J.-P., & Portinha, D. (2015). Toward
replacement of styrene by bio-based methacrylates in unsaturated polyester resins. European
Polymer Journal, 67, 539–550. https://doi.org/10.1016/j.eurpolymj.2015.02.016.
Crapper, G. (2012). Powder coatings.
Crawford, D. M., Bass, R. G., & Haas, T. W. (1998). Strain effects on thermal transitions and
mechanical properties of thermoplastic polyurethane elastomers. Thermochimica Acta,
323(1–2), 53–63. https://doi.org/10.1016/s0040-6031(98)00541-3.
Dai, J., Ma, S., Liu, X., Han, L., Wu, Y., Dai, X., & Zhu, J. (2015). Synthesis of bio-based unsaturated polyester resins and their application in waterborne UV-curable coatings. Progress in
Organic Coatings, 78, 49–54. https://doi.org/10.1016/j.porgcoat.2014.10.007.
Datta, J., Kosiorek, P., & Włoch, M. (2017). Synthesis, structure and properties of poly(etherurethane)s synthesized using a tri-functional oxypropylated glycerol as a polyol.
Journal of Thermal Analysis and Calorimetry, 128(1), 155–167. https://doi.org/10.1007/
s10973-016-5928-2.
De Hoe, G. X., Zumstein, M. T., Tiegs, B. J., Brutman, J. P., McNeill, K., Sander, M., Coates,
G. W., & Hillmyer, M. A. (2018). Sustainable polyester elastomers from lactones: Synthesis,
properties, and enzymatic hydrolyzability. Journal of the American Chemical Society, 140(3),
963–973. https://doi.org/10.1021/jacs.7b10173.
Delebecq, E., Pascault, J.-P., Boutevin, B., & Ganachaud, F. (2012). On the versatility of urethane/
urea bonds: Reversibility, blocked isocyanate, and non-isocyanate polyurethane. Chemical
Reviews, 113(1), 80–118. https://doi.org/10.1021/cr300195n.
Deligny, P., & Tuck, N. (2000). Alkyds & polyesters. Wiley.
Díaz, A., Katsarava, R., & Puiggalí, J. (2014). Synthesis, properties and applications of biodegradable polymers derived from diols and dicarboxylic acids: From polyesters to poly(ester amide)
s. International Journal of Molecular Sciences, 15(5), 7064–7123. https://doi.org/10.3390/
ijms15057064.
Ding, H., Wang, J., Liu, J., Xu, Y., Chen, R., Wang, C., & Chu, F. (2015). Preparation and properties of a novel flame retardant polyurethane quasi-prepolymer for toughening phenolic foam.
Journal of Applied Polymer Science, 132(35). https://doi.org/10.1002/app.42424.
Dodiuk, H., & Goodman, S. H. (Eds.). (2013). Handbook of thermoset plastics (3rd ed. Edition.
ISBN 978-1-4557-3107-7). William Andrew. https://doi.org/10.1016/c2011-0-09694-1.
Domschke, A., Lohmann, D., & Hopken, J. (2000). Polysiloxane-polyol macromers, their preparation and their use. U.S. Patent No. 6,043,328. Washington, DC: U.S. Patent and Trademark
Office. Available in: https://patents.google.com/patent/us6043328a/en
Dušek, K., Špírková, M., & Ilavský, M. (1991). Network formation in polyurethanes due to
allophanate and biuret formation: Gel fraction and equilibrium modulus. Macromolecular
Symposia, 45(1), 87–95. https://doi.org/10.1002/masy.19910450112.
Dutta, N., Karak, N., & Dolui, S. (2004). Synthesis and characterization of polyester resins based
on nahar seed oil. Progress in Organic Coatings, 49(2), 146–152. https://doi.org/10.1016/j.
porgcoat.2003.09.005.
Dyer, E., Taylor, H. A., Mason, S. J., & Samson, J. (1949). The rates of reaction of isocyanates with
alcohols. I. Phenyl isocyanate with 1-and 2-butanol. Journal of the American Chemical Society,
71(12), 4106–4109. https://doi.org/10.1021/ja01180a064.
M. Akbari and R. Najjar