[1] O’Carroll, C. (2004, April). European market update. In Proceedings of the European Laminates Conference and Workshop, Berlin-Germany, 1-12.
[2] Kamrani, S., Moradifar, A., Yadoollahi, S., & Seraian, A. R. (2013). The Investigation on Feasibility of Oriented Strand Boards to Parquet Production from Mixed Residual Veneer Popular and Beech. Iranian Journal of Wood and Paper Industries, 3(2), 25-38, [In Persian].
[3] Gillern, M. F., Oita, K., Teng, R. J., & Tiedeman, G. T. (1981). U. S. Patent No. 4, 264,671. Washington, DC: U. S. Patent and Trademark Office.
[4] Kandelbauer, A., & Teischinger, A. (2009). Dynamic mechanical properties of decorative papers impregnated with melamine formaldehyde resin. European Journal of wood and wood products, 68(2), 179-187.
[5] Özbay, G., Kökten, E. S., & Özçifçi, A. (2021). Synthesis and characterization of resol type phenol-formaldehyde resin improved by SiO2-Np.
[6] Ullah, S., Bustam, M. A., Ahmad, F., Nadeem, M., Naz, M. Y., Sagir, M., & Shariff, A. M. (2015). Synthesis and characterization of melamine formaldehyde resins for decorative paper applications. Journal of the Chinese Chemical Society, 62(2), 182-190.
[7] Weiss, S., Seidl, R., Kessler, W., Kessler, R. W., Zikulnig-Rusch, E. M., & Kandelbauer, A. (2020). Unravelling the phases of melamine formaldehyde resin cure by infrared spectroscopy (FTIR) and multivariate curve resolution (MCR). Polymers, 12(11), 2569.
[8] Erzen, B., Karataş, M., Deniz, Ş., & Aydoğmuş, E. (2024). Advances in Synthesis, Characterization, and Industrial Applications of Phenol Formaldehyde Resins.
[9] Sari, R. K., Fitrianum, F., Kristak, L., Maulana, M. I., Antov, P., Hidayat, W., ... & Adly, M. (2024). Performance of Oriented Strand Board Bonded with a Hybrid Phenol-Formaldehyde/Polymeric Methylene Diphenyl Diisocyanate Adhesives System. BioResources, 19(4).
[10] Galaburda, M., Szewczuk‐Karpisz, K., Goncharuk, O., Siryk, O., Charmas, B., & Deryło‐Marczewska, A. (2024). The influence of sodium alginate on the structural and adsorption properties of resorcinol‐formaldehyde resins and their porous carbon derivatives. ChemPhysChem, 25(4), e202300796.
[11] Galaburda, M., Sternik, D., Chrzanowska, A., Oranska, O., Kovalov, Y., & Derylo-Marczewska, A. (2024). Physicochemical and Adsorption Characterization of Char Derived from Resorcinol–Formaldehyde Resin Modified with Metal Oxide/Silica Nanocomposites. Materials, 17(9), 1981.
[12] Pilato, L. (Ed.). (2010). Phenolic resins: a century of progress (Vol. 11, p. 2010). New York: Springer.
[13] Gardziella, A., Pilato, L. A., & Knop, A. (2013). Phenolic resins: chemistry, applications, standardization, safety and ecology. Springer Science & Business Media.
[14] Zhang, W., Ma, Y., Wang, C., Li, S., Zhang, M., & Chu, F. (2013). Preparation and properties of lignin–phenol–formaldehyde resins based on different biorefinery residues of agricultural biomass. Industrial Crops and Products, 43, 326-333.
[15] Lin, W. S., & Lee, W. J. (2018). Influence of curing temperature on the bonding strength of heat-treated plywood made with melamine-urea-formaldehyde and phenol–formaldehyde resins. European Journal of Wood and Wood Products, 76, 297-303.
[16] Gillern, M. F., Oita, K., Teng, R. J., & Tiedeman, G. T. (1981). U.S. Patent No. 4,264,671. Washington, DC: U.S. Patent and Trademark Office.
[17] Taverna, M. E., Ollearo, R., Moran, J. I., Nicolau, V. V., Estenoz, D. A., & Frontini, P. M. (2015). Mechanical evaluation of laminates based on phenolic resins using lignins as partial substitutes for phenol.
[18] Cardona, F., & Sultan, M. B. H. (2016). Characterization of environmentally sustainable resole phenolic resins synthesized with plant-based bioresources. BioResources, 11(1), 965-983.
[19] Bajia, S. C., Swarnkar, P., Kumar, S., & Bajia, B. (2007). Microwave Assisted Synthesis of Phenol‐Formaldehyde Resole. Journal of Chemistry, 4(4), 457-460.
[20] Hu, X. M., Zhao, Y. Y., & Cheng, W. M. (2015). Effect of formaldehyde/phenol ratio (F/P) on the properties of phenolic resins and foams synthesized at room temperature. Polymer Composites, 36(8),1531-1540.
[21] Gabilondo, N., Larranaga, M., Pena, C., Corcuera, M. A., Echeverría, J. M., & Mondragon, I. (2006). Polymerization of resole resins with several formaldehyde/phenol molar ratios: amine catalysts against sodium hydroxide catalysts. Journal of applied polymer science, 102(3), 2623-2631.
[22] Bhattacharjee, G., Neogi, S., & Das, S. K. (2014). Phenol–formaldehyde runaway reaction: a case study. International Journal of Industrial Chemistry, 5, 1-6.
[23] Zarei, G. M., Ahmadlouydarab, M., & Asadzadeh, N. (2023). Effect of Temperature on Enhanced Oil Recovery from aTwo-Dimensional Porous Medium when Injecting Polyacrylamide Polymer Solution. Iranian Chemical Engineering Journal, 23(130), 117-131, [In Persian].
[24] Ghafouri Taleghani, H. R., Salimi Kkenari, H., & Cheraghi, M. (2024). Investigation of the Controlled Release Behavior of Amoxicillin from Dextran Hydrogels. Iranian Chemical Engineering Journal, 23(135), 46-58, [In Persian].
[25] Khani, M. H., & Gh Khamseh, A. A. (2023). Kinetic, Isotherm, and Thermodynamic Study of Uranium Biosorption by Microalgae Chlorella Vulgaris. Iranian Chemical Engineering Journal, 23(132), 117-131, [In Persian]
[26] Barnes, H. A. (2000). A handbook of elementary rheology. University of Wales, Institute of Non-Newtonian Fluid Mechanics.
[27] Shaghaghi, S., Beheshty, M. H., & Rahimi, H. (2011). Preparation and rheological characterization of phenolic/glass prepregs, [In Persian].
[28] Zhao, C., Zhang, G., & Zhao, L. (2012). Effect of curing agent and temperature on the rheological behavior of epoxy resin systems. Molecules, 17(7), 8587-8594.
[29] Kordani, N., & Vanini, A. S. (2014). Different method to make laminates by shear thickening fluid. Science and Engineering of Composite Materials, 21(3), 421-425.
[30] Gürgen, S. (2019). An investigation on composite laminates including shear thickening fluid under stab condition. Journal of Composite Materials, 53(8), 1111-1122.
[31] Bhattacharjee, G., Neogi, S., & Das, S. K. (2014). Phenol–formaldehyde runaway reaction: a case study. International Journal of Industrial Chemistry, 5, 1-6.
[32] Żmihorska-Gotfryd, A. (2006). Phenol-formaldehyde resols modified by boric acid. Polimery, 51(5), 386-388.
[33] Pizzi, A., & Ibeh, C. C. (2014). Phenol–formaldehydes. In Handbook of thermoset plastics,13-44, William Andrew Publishing.
[34] Li, T., Cao, M., Liang, J., Xie, X., & Du, G. (2017). Theoretical confirmation of the quinone methide hypothesis for the condensation reactions in phenol-formaldehyde resin synthesis. Polymers, 9(2), 45.
[35] Lorenzo, G., Zaritzky, N. E., & Califano, A. N. (2011). Viscoelastic characterization of fluid and gel like food emulsions stabilized with hydrocolloids. Procedia Food Science, 1, 281-286.
[36] Hashemnejad, S. M., & Kundu, S. (2019). Rheological properties and failure of alginate hydrogels with ionic and covalent crosslinks. Soft Matter, 15(39), 7852-7862.
[37] Barnes, H. A. (2000). A handbook of elementary rheology. University of Wales, Institute of Non-Newtonian Fluid Mechanics.
[38] Guseva, D. V., Rudyak, V. Y., Komarov, P. V., Bulgakov, B. A., Babkin, A. V., & Chertovich, A. V. (2018). Dynamic and static mechanical properties of crosslinked polymer matrices: multiscale simulations and experiments. Polymers, 10(7), 792.
