191
Pilch-Pitera, B., Byczyński, Ł., & Myśliwiec, B. (2017). Study on the synthesis of new blocked
polyisocyanates as crosslinking agents for hydrophobic polyurethane powder clear coatings.
Progress in Organic Coatings, 113, 82–89. https://doi.org/10.1016/j.porgcoat.2017.08.011.
Pocius, A. V., & Dillard, D. A. (2002). Adhesion science and engineering: Surfaces, chemistry and
applications. Elsevier.
Prashantha, K., Rashmi, B., & Pai, K. V. K. (2015). Preparation and characterization
of poly(2-hydroxyethyl methacrylate) and castor oil based uralkyds interpenetrating polymer networks. Polymers and Polymer Composites, 23(4), 223–228. https://doi.
org/10.1177/096739111502300403.
Prueitt, R. L., Lynch, H. N., Zu, K., Shi, L., & Goodman, J. E. (2017). Dermal exposure to toluene
diisocyanate and respiratory cancer risk. Environment international, 109, 181–192. https://doi.
org/10.1016/j.envint.2017.09.017.
Raghuraman, A., Babb, D., Miller, M., Paradkar, M., Smith, B., & Nguyen, A. (2016). Sequential
dmc/fab-catalyzed alkoxylation toward high primary hydroxyl, high molecular weight polyether
polyols. Macromolecules, 49(18), 6790–6798. https://doi.org/10.1021/acs.macromol.6b01363.
Raheem, A. B., Noor, Z. Z., Hassan, A., Hamid, M. K. A., Samsudin, S. A., & Sabeen,
A. H. (2019). Current developments in chemical recycling of post-consumer polyethylene terephthalate wastes for new materials production: A review. Journal of Cleaner Production, 225,
1052–1064. https://doi.org/10.1016/j.jclepro.2019.04.019.
Raspoet, G., Nguyen, M. T., McGarraghy, M., & Hegarty, A. F. (1998). The alcoholysis reaction
of isocyanates giving urethanes: Evidence for a multimolecular mechanism. The Journal of
Organic Chemistry, 63(20), 6878–6885. https://doi.org/10.1021/jo9806411.
Rausch Jr, K. W., & Mcclellan, T. R. (1972). Continuous process for the one-shot preparation of a thermoplastic noncellular polyurethane. U.S. Patent No. 3,642,964. Washington,
DC: U.S. Patent and Trademark Office. Available in: https://patents.google.com/patent/
us3642964a/en
Reardon, S., Carrol, A. L., Dumont, J. H., Park, C. H., Lee, K. S., & Labouriau, A. (2019).
Extending the working life of toluene diisocyanate-based polyurethanes. Journal of Applied
Polymer Science, 136(33), 47865. https://doi.org/10.1002/app.47865.
Rivera-Armenta, J., Heinze, T., & Mendoza-Martinez, A. (2004). New polyurethane foams modified with cellulose derivatives. European Polymer Journal, 40(12), 2803–2812. https://doi.
org/10.1016/j.eurpolymj.2004.07.015.
Rogers, M. E., & Long, T. E. (Eds.) (2003). Synthetic methods in step-growth polymers: Wiley. Print
ISBN: 9780471387695. Online ISBN: 9780471220527. https://doi.org/10.1002/0471220523.
Rolph, M. S., Markowska, A. L., Warriner, C. N., & O’Reilly, R. K. (2016). Blocked isocyanates:
From analytical and experimental considerations to non-polyurethane applications. Polymer
Chemistry, 7(48), 7351–7364. https://doi.org/10.1039/c6py01776b.
Sadler, J. M., Toulan, F. R., Palmese, G. R., & La Scala, J. J. (2015). Unsaturated polyester resins
for thermoset applications using renewable isosorbide as a component for property improvement. Journal of Applied Polymer Science, 132(30). https://doi.org/10.1002/app.42315.
Sahoo, S., Kalita, H., Mohanty, S., & Nayak, S. K. (2018). Degradation study of biobased polyester–polyurethane and its nanocomposite under natural soil burial, UV radiation and hydrolyticsalt water circumstances. Journal of Polymers and the Environment, 26(4), 1528–1539. https://
doi.org/10.1007/s10924-017-1058-6.
Salla, J., Ramis, X., Morancho, J., & Cadenato, A. (2002). Isoconversional kinetic analysis of a
carboxyl terminated polyester resin crosslinked with triglycidyl isocyanurate (TGIC) used in
powder coatings from experimental results obtained by DSC and TMDSC. Thermochimica
Acta, 388(1–2), 355–370. https://doi.org/10.1016/s0040-6031(02)00036-9.
Saralegi, A., Rueda, L., Fernández-d’Arlas, B., Mondragon, I., Eceiza, A., & Corcuera,
M. A. (2013). Thermoplastic polyurethanes from renewable resources: Effect of soft segment chemical structure and molecular weight on morphology and final properties. Polymer
International, 62(1), 106–115. https://doi.org/10.1002/pi.4330.
8 Reactive and Functional Polyesters and Polyurethanes
Pilch-Pitera, B., Byczyński, Ł., & Myśliwiec, B. (2017). Study on the synthesis of new blocked
polyisocyanates as crosslinking agents for hydrophobic polyurethane powder clear coatings.
Progress in Organic Coatings, 113, 82–89. https://doi.org/10.1016/j.porgcoat.2017.08.011.
Pocius, A. V., & Dillard, D. A. (2002). Adhesion science and engineering: Surfaces, chemistry and
applications. Elsevier.
Prashantha, K., Rashmi, B., & Pai, K. V. K. (2015). Preparation and characterization
of poly(2-hydroxyethyl methacrylate) and castor oil based uralkyds interpenetrating polymer networks. Polymers and Polymer Composites, 23(4), 223–228. https://doi.
org/10.1177/096739111502300403.
Prueitt, R. L., Lynch, H. N., Zu, K., Shi, L., & Goodman, J. E. (2017). Dermal exposure to toluene
diisocyanate and respiratory cancer risk. Environment international, 109, 181–192. https://doi.
org/10.1016/j.envint.2017.09.017.
Raghuraman, A., Babb, D., Miller, M., Paradkar, M., Smith, B., & Nguyen, A. (2016). Sequential
dmc/fab-catalyzed alkoxylation toward high primary hydroxyl, high molecular weight polyether
polyols. Macromolecules, 49(18), 6790–6798. https://doi.org/10.1021/acs.macromol.6b01363.
Raheem, A. B., Noor, Z. Z., Hassan, A., Hamid, M. K. A., Samsudin, S. A., & Sabeen,
A. H. (2019). Current developments in chemical recycling of post-consumer polyethylene terephthalate wastes for new materials production: A review. Journal of Cleaner Production, 225,
1052–1064. https://doi.org/10.1016/j.jclepro.2019.04.019.
Raspoet, G., Nguyen, M. T., McGarraghy, M., & Hegarty, A. F. (1998). The alcoholysis reaction
of isocyanates giving urethanes: Evidence for a multimolecular mechanism. The Journal of
Organic Chemistry, 63(20), 6878–6885. https://doi.org/10.1021/jo9806411.
Rausch Jr, K. W., & Mcclellan, T. R. (1972). Continuous process for the one-shot preparation of a thermoplastic noncellular polyurethane. U.S. Patent No. 3,642,964. Washington,
DC: U.S. Patent and Trademark Office. Available in: https://patents.google.com/patent/
us3642964a/en
Reardon, S., Carrol, A. L., Dumont, J. H., Park, C. H., Lee, K. S., & Labouriau, A. (2019).
Extending the working life of toluene diisocyanate-based polyurethanes. Journal of Applied
Polymer Science, 136(33), 47865. https://doi.org/10.1002/app.47865.
Rivera-Armenta, J., Heinze, T., & Mendoza-Martinez, A. (2004). New polyurethane foams modified with cellulose derivatives. European Polymer Journal, 40(12), 2803–2812. https://doi.
org/10.1016/j.eurpolymj.2004.07.015.
Rogers, M. E., & Long, T. E. (Eds.) (2003). Synthetic methods in step-growth polymers: Wiley. Print
ISBN: 9780471387695. Online ISBN: 9780471220527. https://doi.org/10.1002/0471220523.
Rolph, M. S., Markowska, A. L., Warriner, C. N., & O’Reilly, R. K. (2016). Blocked isocyanates:
From analytical and experimental considerations to non-polyurethane applications. Polymer
Chemistry, 7(48), 7351–7364. https://doi.org/10.1039/c6py01776b.
Sadler, J. M., Toulan, F. R., Palmese, G. R., & La Scala, J. J. (2015). Unsaturated polyester resins
for thermoset applications using renewable isosorbide as a component for property improvement. Journal of Applied Polymer Science, 132(30). https://doi.org/10.1002/app.42315.
Sahoo, S., Kalita, H., Mohanty, S., & Nayak, S. K. (2018). Degradation study of biobased polyester–polyurethane and its nanocomposite under natural soil burial, UV radiation and hydrolyticsalt water circumstances. Journal of Polymers and the Environment, 26(4), 1528–1539. https://
doi.org/10.1007/s10924-017-1058-6.
Salla, J., Ramis, X., Morancho, J., & Cadenato, A. (2002). Isoconversional kinetic analysis of a
carboxyl terminated polyester resin crosslinked with triglycidyl isocyanurate (TGIC) used in
powder coatings from experimental results obtained by DSC and TMDSC. Thermochimica
Acta, 388(1–2), 355–370. https://doi.org/10.1016/s0040-6031(02)00036-9.
Saralegi, A., Rueda, L., Fernández-d’Arlas, B., Mondragon, I., Eceiza, A., & Corcuera,
M. A. (2013). Thermoplastic polyurethanes from renewable resources: Effect of soft segment chemical structure and molecular weight on morphology and final properties. Polymer
International, 62(1), 106–115. https://doi.org/10.1002/pi.4330.
8 Reactive and Functional Polyesters and Polyurethanes