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Journal articles on the topic 'Polymeric isocyanate resin'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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1

Buckley, C. J., C. Phanopoulos, N. Khaleque, A. Engelen, M. E. J. Holwill, and A. G. Michette. "Examination of the Penetration of Polymeric Methylene Di-Phenyl-Di-Isocyanate (pMDI) into Wood Structure Using Chemical-State X-Ray Microscopy." Holzforschung 56, no. 2 (2002): 215–22. http://dx.doi.org/10.1515/hf.2002.035.

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Summary The penetration behaviour of isocyanate-based wood resins was evaluated using x-ray microscopy. Aspen wood pieces were bonded together in a controlled manner. These were embedded in a methacrylate-based resinand thin sections were prepared, cut from the transverse face of thewoodcomposite. X-ray images of these sections were prepared at several selected x-ray energies to allow the isocyanate, cellulose, lignin and the embedding agent distributions to be mapped. The isocyanate resin was found to penetrate deeply into the wood. The resin enters large cell lumen, and wicks along the inner

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2

Asafu-Adjaye, Osei, Brian Via, and Sujit Banerjee. "Increasing Cold Tack of Polymeric Methylene Diphenyl Diisocyanate Resin with Partial Soy Flour Substitution." Forest Products Journal 70, no. 1 (2020): 143–44. http://dx.doi.org/10.13073/fpj-d-19-00049.

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Abstract Partial substitution of polymeric methylene diphenyl diisocyanate resin with soy flour increases the cold tack of the resin to the level achieved by urea formaldehyde resin. The tack can be fine-tuned by adjusting the amount of soy flour added. The increase in tack is caused by the reaction of the isocyanate resin with the water contained in soy flour, as well as with hydroxyl and other groups present in soy flour components. The higher cold tack should increase the stability of pre-press mats, especially in particleboard manufacturing.

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3

Gruver, T. Michael, and Nicole R. Brown. "Penetration and performance of isocyanate wood binders on selected wood species." BioResources 1, no. 2 (2006): 233–47. http://dx.doi.org/10.15376/biores.1.2.233-247.

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The penetration and performance of polymeric diphenylmethane diisocyanate (pMDI) wood binder was investigated according to three factors: substrate species (aspen, yellow-poplar, or southern yellow pine); anatomical bonding plane (radial or tangential); and moisture content (0%, 5%, or 12%). Compression shear block tests and fluorescence microscopy were used to examine bond performance and resin penetration. Statistically, each of the aforementioned factors impacted results. As moisture content increased, observed bond strengths and wood failure increased. Bond formation did not occur when the

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4

Wu, Guomin, Xinhao Feng, Can Jin, Zhenwu Kong, and Siqun Wang. "Effect of lignin-containing cellulose nanofibrils on the curing kinetics of polymeric diphenylmethane diisocyanate (PMDI) resin." Holzforschung 73, no. 9 (2019): 879–87. http://dx.doi.org/10.1515/hf-2018-0253.

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Abstract In order to increase the curing rate of polymeric diphenylmethane diisocyanate (PMDI) resin, different contents of lignin-containing cellulose nanofibrils (L-CNFs) were blended into the PMDI. Differential scanning calorimetry (DSC) was used to examine how the addition of L-CNFs influences the curing kinetics of PMDI resin. The activation energy (Ea) of the curing reaction of PMDI/L-CNF systems was calculated using the Kissinger, Friedman and Flynn-Wall-Ozawa model-free methods. The results showed that Ea values calculated by the aforementioned three methods varied in a similar trend w

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5

Zhu, Li Bin, Bo Han, Ji You Gu, Yan Hua Zhang, Hai Yan Tan, and Ying Feng Zuo. "Preparation of Water-Resistance Plywood with UF Resin Modified by Emulsifiable Polyisocyanate." Applied Mechanics and Materials 26-28 (June 2010): 1056–60. http://dx.doi.org/10.4028/www.scientific.net/amm.26-28.1056.

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The purpose of the study was to manufacture water-resistance plywood with using UF resin modified by emulsifiable polyisocyanate. The emulsifiable polyisocyanate which contains plenty of hydrophilic segments and teminal isocyanate groups were synthesized by reaction between various kinds of polyether polyols and polymeric methane dipthenyl diisocyanate (pMDI). A type of composite adhesive was obtained from the mixture of emulsifiable polyisocyanate and urea formaldehyde resin. The process parameters, such as the molar ratio of –NCO and –OH, mass fraction of emulsifiable polyisocyanate in UF re

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6

Barreto, Maria I. M., Victor De Araujo, Juliana Cortez-Barbosa, André L. Christoforo, and Jorge D. M. Moura. "Structural performance analysis of cross-laminated timber-bamboo (CLTB)." BioResources 14, no. 3 (2019): 5045–58. http://dx.doi.org/10.15376/biores.14.3.5045-5058.

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Construction systems based on cross-laminated timber (CLT) have versatility in material development and are an interesting alternative for construction. This study evaluated the structural performance of cross-laminated timber-bamboo produced from wood (Pinus spp.) and bamboo (Dendrocalamus giganteus). Panels were produced by strips (wood and bamboo) assorted, under non-destructive structural grading, to support a better panel configuration. Small-length pine pieces were also included in the study, considering their low added-value and underutilization in sawmills from Telêmaco Borba, Brazil.

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7

Aristri, Manggar Arum, Muhammad Adly Rahandi Lubis, Sumit Manohar Yadav, et al. "Recent Developments in Lignin- and Tannin-Based Non-Isocyanate Polyurethane Resins for Wood Adhesives—A Review." Applied Sciences 11, no. 9 (2021): 4242. http://dx.doi.org/10.3390/app11094242.

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This review article aims to summarize the potential of using renewable natural resources, such as lignin and tannin, in the preparation of NIPUs for wood adhesives. Polyurethanes (PUs) are extremely versatile polymeric materials, which have been widely used in numerous applications, e.g., packaging, footwear, construction, the automotive industry, the lighting industry, insulation panels, bedding, furniture, metallurgy, sealants, coatings, foams, and wood adhesives. The isocyanate-based PUs exhibit strong adhesion properties, excellent flexibility, and durability, but they lack renewability. T

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8

Lattimer, M. B., C. D. Weber, and Z. R. Hardt. "An Improved Adhesive System for Textile-Reinforced Rubber Products." Rubber Chemistry and Technology 58, no. 2 (1985): 383–91. http://dx.doi.org/10.5254/1.3536072.

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Abstract Resorcinol Formaldehyde Latex (RFL) adhesive systems have been used for over forty years to bond synthetic fibers to rubber compounds. The original RFL formulation was developed by Charch and Maney. The adhesive was applied primarily to rayon fibers and later extended to nylon and glass fibers. At the same time, the formulation evolved with the introduction of synthetic latexes and preformed resorcinol formaldehyde resin solutions. The RFL treated fibers are used to reinforce rubber products (e.g., tires, conveyor belts, hoses, V-belts). With the commercialization of polyester fibers,

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9

Pachha, R. R., J. R. Thakkar, and R. D. Patel. "Studies of vinyl ester resins and their urethanized derivatives." High Performance Polymers 5, no. 3 (1993): 207–12. http://dx.doi.org/10.1088/0954-0083/5/3/004.

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The epoxy resins diglycidyl ether of bisphenol A and triglycidyl p-amino phenol were reacted with acrylic acid to afford the corresponding acrylated resins. These vinyl ester resins were then reacted with toluene di-isocyanate to procure their urethanized derivatives. All these resins were characterized by their viscosity, number average molecular weight and infrared spectrophotometry. Curingconditions for these resins were established by differential scanning calorimetry. The results indicated that the curing reaction follows first-order kinetics, with activation energy in the range 53-84 kJ

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10

Jorda, Johannes, Günther Kain, Marius-Catalin Barbu, Alexander Petutschnigg, and Pavel Král. "Influence of Adhesive Systems on the Mechanical and Physical Properties of Flax Fiber Reinforced Beech Plywood." Polymers 13, no. 18 (2021): 3086. http://dx.doi.org/10.3390/polym13183086.

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In order to improve the acceptance of broader industrial application of flax fiber reinforced beech (Fagus sylvatica L.) plywood, five different industrial applicated adhesive systems were tested. Epoxy resin, urea-formaldehyde, melamine-urea formaldehyde, isocyanate MDI prepolymer, and polyurethane displayed a divergent picture in improving the mechanical properties—modulus of elasticity, modulus of rupture, tensile strength, shear strength and screw withdrawal resistance—of flax fiber-reinforced plywood. Epoxy resin is well suited for flax fiber reinforcement, whereas urea-formaldehyde, mela

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11

Franke, J. "Isocyanate-Based Casting Resins." Journal of Cellular Plastics 27, no. 1 (1991): 65–66. http://dx.doi.org/10.1177/0021955x9102700182.

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12

Chen, Lijun, Wen Li, and Wei Jiang. "Synthesis and application of cationic fluorinated acrylic resin for use in cathodic electrodeposition coatings." Pigment & Resin Technology 43, no. 5 (2014): 251–55. http://dx.doi.org/10.1108/prt-10-2013-0093.

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Purpose – The purpose of this paper was to prepare a fluorinated acrylate resin, which would be synthesised via solution polymerisation of fluorinated monomer, acrylate monomers and other functional monomers. Relevant characterisation and application studies were also carried out. Fluorinated polymers are expected to be adopted in specific coatings to afford outstanding advantages, such as high chemical and photochemical resistance, low surface tension and low refractive index. At present, fluorinated cathodic electrodeposition (CED) coatings are attracting the attention that they deserve and

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13

Lubis, Muhammad Adly Rahandi, Byung-Dae Park, and Sang-Min Lee. "Microencapsulation of polymeric isocyanate for the modification of urea-formaldehyde resins." International Journal of Adhesion and Adhesives 100 (July 2020): 102599. http://dx.doi.org/10.1016/j.ijadhadh.2020.102599.

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14

Cardamone, Jeanette M. "Reacting Cotton Cellulose with Lignin-Based Polyurethane." Textile Research Journal 62, no. 7 (1992): 371–81. http://dx.doi.org/10.1177/004051759206200702.

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Chain-extended lignin was reacted with blocked isocyanate and the product, lignin polyurethane (LPU), was subsequently applied by padding to cotton print cloth at three add-on levels: 1.70, 3.45, and 4.30%. Product syntheses and reactivity were followed by FTIR spectroscopy. LPU as a formaldehyde-free finish improved durable press (DP) and dimensional stability of the unfinished cloth, but the improvement was less than conventional amino resin finishes. Unlike conventional resin finishes, LPU showed strength and abrasion resistance retention. Abrasion resistance improved at the 3.5% add-on lev

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15

Aristri, Manggar Arum, Muhammad Adly Rahandi Lubis, Raden Permana Budi Laksana, et al. "Bio-Polyurethane Resins Derived from Liquid Fractions of Lignin for the Modification of Ramie Fibers." Jurnal Sylva Lestari 9, no. 2 (2021): 223. http://dx.doi.org/10.23960/jsl29223-238.

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In this study, technical lignin from black liquor was used as a pre-polymer for the preparation of bio-polyurethane (Bio-PU) resins. Briefly, the isolated lignin was fractionated using ethyl acetate (EtAc) and methanol (MeOH). The liquid fractions of lignin, such as lignin-EtAc (L-EtAc) and lignin-methanol (L-MeOH), were mixed with 10% of polymeric isocyanate (based on the weight of liquid fractions) to obtain Bio-PU resins. The isolated lignin, fractionated lignin, and lignin-derived Bio-PU resins were characterized using several techniques. The obtained Bio-PU resins were then used to modify

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16

Hao, Zhi Feng, Xue Mei Wang, Hong Xia Hou, Ya Hong Wu, Hua Gong Li, and Jian Yu. "Study on the Chemical Modification of Titanium-Doped Silicone Using Hydroxyl-Terminated Saturated Polyester." Advanced Materials Research 239-242 (May 2011): 2817–21. http://dx.doi.org/10.4028/www.scientific.net/amr.239-242.2817.

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In this paper, a kind of titanium-doped silicone prepolymer(TDS) was modified by hydroxyl-terminated saturated polyester (HTSP) by condensation polymerization. By Fourier Transform Infrared Spectroscopy (FTIR) the reaction of ethoxy groups of the TDS prepolymer with hydroxyl groups of the HTSP during condensation polymerization process was conﬁrmed. The resins were cured with blocked polymeric isocyanate. The inﬂuence of the HTSP content on the properties of the modified resins such as thermal stability, corrosion resistance, as well as mechanical and other properties, were discussed in detail

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17

Duff, David W., and Gary E. Maciel. "Monitoring postcure reaction chemistry of residual isocyanate in 4,4'-methylenebis(phenyl isocyanate) based isocyanurate resins by nitrogen-15 and carbon-13 CP/MAS NMR." Macromolecules 24, no. 2 (1991): 387–97. http://dx.doi.org/10.1021/ma00002a008.

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18

Barcia, Fábio L., Márcio A. Abrahão, and Bluma G. Soares. "Modification of epoxy resin by isocyanate-terminated polybutadiene." Journal of Applied Polymer Science 83, no. 4 (2001): 838–49. http://dx.doi.org/10.1002/app.10079.

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19

Kadurina, T. I., V. A. Prokopenko, and S. I. Omelchenko. "Studies of interactions in oligomeric epoxy resin-isocyanate systems." European Polymer Journal 22, no. 11 (1986): 865–70. http://dx.doi.org/10.1016/0014-3057(86)90062-5.

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20

Yang, J. F., and T. L. Yu. "The Curing Reaction of Isocyanate-Thickened Unsaturated Polyester Resin." Journal of Macromolecular Science, Part A 31, no. 4 (1994): 427–38. http://dx.doi.org/10.1080/10601329409351529.

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21

Yang, J. F., and T. L. Yu. "The Curing Reaction of Isocyanate-Thickened Unsaturated Polyester Resin." Journal of Macromolecular Science, Part A 31, no. 4 (1994): 427–38. http://dx.doi.org/10.1080/10601329408545295.

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22

Chen, Xinyi, Antonio Pizzi, Hisham Essawy, et al. "Non-Furanic Humins-Based Non-Isocyanate Polyurethane (NIPU) Thermoset Wood Adhesives." Polymers 13, no. 3 (2021): 372. http://dx.doi.org/10.3390/polym13030372.

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Predominantly non-furanic commercial humins were used to prepare humin-based non-isocyanate polyurethane (NIPU) resins for wood panel adhesives. Pure humin-based NIPU resins and tannin–humin NIPU resins were prepared, the latter to upgrade the humins’ performance. Species in the raw humins and species formed in the NIPU resins were identified by Matrix Assisted Laser Desorption Ionization Time of Flight (MALDI ToF) spectrometry and Fourier Transform Infrared (FTIR). Humins, fulvic acid and derivatives, humic acid and its fragments, some lignans present and furanic oligomers present formed NIPU

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23

Wang, Na, Xinhui Wang, Jinyan Lang, Zhenhua Hu, and Heng Zhang. "Synthesis and Characterization of Hyperbranched and Organosilicone Modified Waterborne Polyurethane Acrylates Photosensitive Resin." Polymers 13, no. 13 (2021): 2039. http://dx.doi.org/10.3390/polym13132039.

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A new type of waterborne polyurethane acrylate was synthesized for use as a UV curing coating. The N,N-dihydroxy methyl ethyl-3-Methyl aminopropanoate monomer was first prepared via adding reactions of methyl acrylate and diethanol amine with methyl alcohol as the solvent. Then, the hyperbranched prepolymer was obtained by addition of trimethylolpropane with toluenesulfonic acid as catalyst and N,N-dimethyl formamide as solvent. The resulting hyperbranched and organosilicone modified waterborne polyurethane acrylates was synthesized through the mixed reaction of prepolymer and Hydroxy silicone

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24

Soares, Bluma G., Viviane Gonçalez, Rurik Galimberti, Alex S. Sirqueira, Fabio L. Barcia, and Renata A. Simão. "Toughening of an epoxy resin with an isocyanate-terminated polyether." Journal of Applied Polymer Science 108, no. 1 (2008): 159–66. http://dx.doi.org/10.1002/app.26991.

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25

Shih, Wen-Chang, Chen-Chi M. Ma, Jen-Chang Yang, and Hung-De Chen. "Polydimethylsiloxane containing isocyanate group-modified epoxy resin: Curing, characterization, and properties." Journal of Applied Polymer Science 73, no. 13 (1999): 2739–47. http://dx.doi.org/10.1002/(sici)1097-4628(19990923)73:13<2739::aid-app22>3.0.co;2-f.

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26

Soares, Bluma G., Viviane Gonçalez, Rurik Galimberti, Fabio L. Barcia, and Alex S. Sirqueira. "Polyester containing isocyanate groups-Modified epoxy resin: Rheological, dynamic-mechanical, and impact properties." Polymer Engineering & Science 48, no. 10 (2008): 1917–22. http://dx.doi.org/10.1002/pen.21035.

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27

Sendijarevic, Vahid, Aisa Sendijarevic, Kurt C. Frisch, and Paul Reulen. "Novel isocyanate-based matrix resins for high temperature composite applications." Polymer Composites 17, no. 2 (1996): 180–86. http://dx.doi.org/10.1002/pc.10603.

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28

Chen, Yahn-Haur, and Chin-Ping Yang. "Coemulsion and electrodeposition properties of mixtures of cationic epoxy resin and cationic acrylic resin containing blocked-isocyanate groups." Journal of Applied Polymer Science 51, no. 9 (1994): 1539–47. http://dx.doi.org/10.1002/app.1994.070510903.

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29

Guo, Baochun, Weiwen Fu, Demin Jia, Qinghua Qiu, and Lei Wang. "Cure Behaviour and Structure of Dicyanate-Epoxy Novolac Blends." Polymers and Polymer Composites 10, no. 3 (2002): 237–48. http://dx.doi.org/10.1177/096739110201000306.

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The cure characteristics of bisphenol A dicyanate-novolac epoxy resin blends were investigated by gel time determination and dynamic DSC. The effects of the proportion on the structures of cured blends were investigated by FTIR. In situ FTIR was utilized to study the curing mechanism and curing kinetics. The results indicated the distinct catalytic effects of the novolac epoxy resin on the curing of bisphenol A dicyanate. Due to considerable amounts of unepoxidized phenol present in the novolac epoxy resin, the reactions between phenol and cyanate disturbed the formation of the co-reaction pro

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30

Lubis, Muhammad Adly Rahandi, Byung-Dae Park, and Sang-Min Lee. "Modification of urea-formaldehyde resin adhesives with blocked isocyanates using sodium bisulfite." International Journal of Adhesion and Adhesives 73 (March 2017): 118–24. http://dx.doi.org/10.1016/j.ijadhadh.2016.12.001.

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31

Miyazaki, Junko, and Takato Nakano. "Fracture behavior of laminated wood bonded with water based polymer-isocyanate resin and resorcinol-formaldehyde resin under impact fatigue." Journal of Applied Polymer Science 109, no. 1 (2008): 276–81. http://dx.doi.org/10.1002/app.27457.

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32

Balakrishna, R. S., M. N. Sathyanarayana, B. Balaji Vishwanath, and M. M. Shirsalkar. "Cathodically depositable systems based on epoxy resin and blocked isocyanates with cardanol." Journal of Applied Polymer Science 41, no. 78 (1990): 1365–72. http://dx.doi.org/10.1002/app.1990.070410701.

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33

Kieffer, A., A. Hartwig, G. Schmidt-Naake, and O. D. Hennemann. "Reactions at the interphase between an isocyanate and epoxy resins — infrared spectroscopic investigations." Acta Polymerica 49, no. 12 (1998): 720–24. http://dx.doi.org/10.1002/(sici)1521-4044(199812)49:12<720::aid-apol720>3.0.co;2-4.

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34

ZMIHORSKA-GOTFRYD, ANNA. "Polymer compositions based on butoxylated melamine-formaldehyde resin modified with urethane prepolymers with isocyanate end-groups." Polimery 48, no. 04 (2003): 280–87. http://dx.doi.org/10.14314/polimery.2003.280.

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35

Lonikar, S. V., N. Rungsimuntakul, R. D. Gilbert, and R. E. Fornes. "The effect of masked isocyanates on the moisture absorption of MY 720/DDS epoxy resin." Journal of Polymer Science Part A: Polymer Chemistry 28, no. 4 (1990): 759–75. http://dx.doi.org/10.1002/pola.1990.080280406.

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36

Liu, Kuan-Liang, Pei-Yu Kuo, Jin-Lin Han, and Kuo-Huang Hsieh. "Influence of Bioadditives Made from Sugarcane Bagasse on Interpenetrating Polymer Networks." International Journal of Polymer Science 2020 (July 25, 2020): 1–15. http://dx.doi.org/10.1155/2020/8084940.

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To achieve a sustainable bioeconomy, various bioderived additives have been developed to produce biocomposites, but only a handful of research on biocomposites focuses on the effect of bioderived additives on interpenetrating polymer networks (IPNs). This study is aimed at understanding the interaction between bioadditives and interpenetrating polymer networks and is the first study to build the relationship between bioadditive ratio and damping factor based on dynamic mechanical analysis. The IPNs were prepolymerized in bulk by isocyanate and poly(oxypropylene) polyol (PPG) with two different

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37

Keijsers, Edwin, Martien van den Oever, Jan van Dam, Aad Lansbergen, Cor Koning, and Harald van den Akker. "The development of reed composite fiber boards using partially bio-based, formaldehyde- and monomeric isocyanate-free resins." Reinforced Plastics 64, no. 4 (2020): 195–203. http://dx.doi.org/10.1016/j.repl.2019.10.007.

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38

Ji, Youngyoun, Jinhwan Kim, and Jin-Young Bae. "Flame-retardant ABS resins from novel phenyl isocyanate blocked novolac phenols and triphenyl phosphate." Journal of Applied Polymer Science 102, no. 1 (2006): 721–28. http://dx.doi.org/10.1002/app.23258.

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39

Chang, Chang-Pin, Cheng-Hung Shih, Jhu-Lin You, Meng-Jey Youh, Yih-Ming Liu, and Ming-Der Ger. "Preparation and Ballistic Performance of a Multi-Layer Armor System Composed of Kevlar/Polyurea Composites and Shear Thickening Fluid (STF)-Filled Paper Honeycomb Panels." Polymers 13, no. 18 (2021): 3080. http://dx.doi.org/10.3390/polym13183080.

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In this study, the ballistic performance of armors composed of a polyurea elastomer/Kevlar fabric composite and a shear thickening fluid (STF) structure was investigated. The polyurea used was a reaction product of aromatic diphenylmethane isocyanate (A agent) and amine-terminated polyether resin (B agent). The A and B agents were diluted, mixed and brushed onto Kevlar fabric. After the reaction of A and B agents was complete, the polyurea/Kevlar composite was formed. STF structure was prepared through pouring the STF into a honeycomb paper panel. The ballistic tests were conducted with refere

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40

Kieffer, Andreas, and Andreas Hartwig. "Interphase Reaction of Isocyanates with Epoxy Resins Containing Functional Groups of Different Reactivity." Macromolecular Materials and Engineering 286, no. 4 (2001): 254–59. http://dx.doi.org/10.1002/1439-2054(20010401)286:4<254::aid-mame254>3.0.co;2-l.

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41

Sankar, S. S., S. V. Lonikar, R. D. Gilbert, R. E. Fornes, and E. O. Stejskal. "Solid-state cpmas 13C-NMR studies of the reaction of an epoxy resin with masked isocyanates." Journal of Polymer Science Part B: Polymer Physics 28, no. 3 (1990): 293–302. http://dx.doi.org/10.1002/polb.1990.090280304.

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42

Umemura, Kenji, Akihiro Takahashi, and Shuichi Kawai. "Durability of isocyanate resin adhesives for wood. II. Effect of the addition of several polyols on the thermal properties." Journal of Applied Polymer Science 74, no. 7 (1999): 1807–14. http://dx.doi.org/10.1002/(sici)1097-4628(19991114)74:7<1807::aid-app24>3.0.co;2-0.

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43

Wachenfeld-Eisele, E., and W. Burchard. "Solution properties of amine-cured epoxy resins based on triglycidyl isocyanurate: semidilute solutions." Macromolecules 22, no. 5 (1989): 2496–501. http://dx.doi.org/10.1021/ma00195a085.

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44

Yoon, Chul-Hyun, Jin-Sup Shin, In-Woo Cheong, Doug-Youn Lee, Young-Jun Park, and Jung-Hyun Kim. "Effect of interfacial crosslinking on miscibility behavior between isocyanate-functionalized poly(n-butyl methacrylate) particles and carboxylic alkali-soluble resin." Journal of Applied Polymer Science 90, no. 3 (2003): 792–98. http://dx.doi.org/10.1002/app.12566.

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45

Duan, Huajun, Sa Ji, Jie Chen, and Bo Zhang. "Effects of phthalic anhydride polyester polyol on mechanical properties of polyurethane resin system based on polymethylene polyphenyl isocyanate-polypropylene glycol." Plastics, Rubber and Composites 47, no. 9 (2018): 413–21. http://dx.doi.org/10.1080/14658011.2018.1517139.

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46

Sun, Weihong, Xin Yan, and Xi Zhu. "Dynamic mechanical and underwater acoustic properties of the polyurethane/epoxy resin blend elastomers filled with macroporous poly(vinyl acetate-co-triallyl isocyanurate) resin beads." Journal of Applied Polymer Science 122, no. 4 (2011): 2359–67. http://dx.doi.org/10.1002/app.34112.

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47

Despres, A., A. Pizzi, and L. Delmotte. "13C NMR investigation of the reaction in water of UF resins with blocked emulsifiable isocyanates." Journal of Applied Polymer Science 99, no. 2 (2005): 589–96. http://dx.doi.org/10.1002/app.22498.

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48

Duff, David W., and Gary E. Maciel. "Carbon-13 and nitrogen-15 CP/MAS NMR characterization of biuret-rich 4,4'-methylenebis(phenyl isocyanate)-based resins." Macromolecules 23, no. 20 (1990): 4367–71. http://dx.doi.org/10.1021/ma00222a007.

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Sienkiewicz, A., and P. Czub. "Blocked isocyanates as alternative curing agents for epoxy-polyurethane resins based on modified vegetable oils." Express Polymer Letters 13, no. 7 (2019): 642–55. http://dx.doi.org/10.3144/expresspolymlett.2019.54.

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Leu, Tsu-Shang. "Structure and characterization for conterminously linked polymer of short-chain epoxy resin with triallyl isocyanurate and bismaleimide." Journal of Applied Polymer Science 102, no. 3 (2006): 2470–80. http://dx.doi.org/10.1002/app.24585.

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