2001
DOI: 10.1016/s0300-9440(01)00239-9
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Pathways targeting solvent-free PUR coatings

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Cited by 17 publications
(14 citation statements)
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“…In the development of high solid polyurethane coatings, as for epoxy coatings, the adopted approach is to lower the binder of the resin, add diluents or lower the viscosity of the polyisocyanate crosslinking agent [84,111,116,117]. Renz et al [118] described the effect of these modifications and their possible negative effects. Hydroxy-terminated polyester and hydroxy-functional acrylic resins are the most common polyols used in the formulation of high solid polyurethane coatings [84,116].…”
Section: High Solid Polyurethane Coatingsmentioning
confidence: 99%
“…In the development of high solid polyurethane coatings, as for epoxy coatings, the adopted approach is to lower the binder of the resin, add diluents or lower the viscosity of the polyisocyanate crosslinking agent [84,111,116,117]. Renz et al [118] described the effect of these modifications and their possible negative effects. Hydroxy-terminated polyester and hydroxy-functional acrylic resins are the most common polyols used in the formulation of high solid polyurethane coatings [84,116].…”
Section: High Solid Polyurethane Coatingsmentioning
confidence: 99%
“…All products were isolated in >99% purity with the exception of the sample with n = 4 and R = NCO (>98%), as confirmed by 700-MHz 1 H NMR and 13 C NMR spectroscopies and GPC, in most cases limited only by the detection level of the equipment (data not shown). Because of the strong emphasis on purity, no yields were determined.…”
Section: Synthesis Of Isocyanuratesmentioning
confidence: 73%
“…The combined resin-fraction was then distilled in a thin-film shortpath evaporator at 220°C and <10 À7 mbar, collecting the distillate as a very slightly greenish transparent viscous oil. The distillate was evaporated using a thin-film short-path evaporator at 160°C and <10 À7 mbar, collecting the pure product as resin as a very slightly greenish transparent viscous oil, characterized by (numbers for HDI-trimer) 1 H-NMR (700 MHz, C 6 D 6 ): δ = 3.78 (2H, t), 2.54 (2H, t), 1.53 (2H, quin), and 1.03-0.92 (6H, m) ppm; 13 …”
Section: Synthesis Of Functional Isocyanuratesmentioning
confidence: 99%
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