2017
DOI: 10.1016/j.porgcoat.2017.08.011
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Study on the synthesis of new blocked polyisocyanates as crosslinking agents for hydrophobic polyurethane powder clear coatings

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Cited by 18 publications
(7 citation statements)
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“…The symmetrical bending vibration and strong absorption of CH appear at 2937 and 1670 cm −1 , respectively, because of the tensile vibration of surface OH and CO in the GO. The absorption peak at 1543 cm −1 comes from amide or carbamate, corresponding to the coupling of CHN deformation vibration [34]. The infrared spectrum contains absorption peaks related to Tri‐HDI groups, indicating that chemical reaction, not just absorption or intercalation, occurred between GO and Tri‐HDI.…”
Section: Resultsmentioning
confidence: 99%
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“…The symmetrical bending vibration and strong absorption of CH appear at 2937 and 1670 cm −1 , respectively, because of the tensile vibration of surface OH and CO in the GO. The absorption peak at 1543 cm −1 comes from amide or carbamate, corresponding to the coupling of CHN deformation vibration [34]. The infrared spectrum contains absorption peaks related to Tri‐HDI groups, indicating that chemical reaction, not just absorption or intercalation, occurred between GO and Tri‐HDI.…”
Section: Resultsmentioning
confidence: 99%
“…The symmetrical bending vibration and strong absorption of C H appear at 2937 and 1670 cm À1 , respectively, because of the tensile vibration of surface OH and C O in the GO. The absorption peak at 1543 cm À1 comes from amide or carbamate, corresponding to the coupling of CHN deformation vibration [34] carbon-nitrogen stretching vibration and the CHN deformation vibration. The CHN group weakened the hydrogen bonds between adjacent layers in the GO, and thus the GO flakes were peeled off in polar aprotic solvents.…”
Section: Functional Group Structurementioning
confidence: 99%
“…In step 2, the sample shows a thermal weight loss of 36.14%, and the DSC curve exhibits an obvious endothermic peak (P1). Since the unblocking temperature of the CPL-blocked -NCO group is generally between 130-250°C, the mass and energy change of step 2 is mainly caused by the unblocking of the C 3 IPTS terminal group [38,44,45]. In other words, the CPL of C 3 IPTS is released at this stage, and the -NCO group is exposed.…”
Section: Characterization and Mechanical Testingmentioning
confidence: 99%
“…53 This is additional evidence of the catalytic effect of calcein during polymerization. From the NMR spectra of PUs before degradation (Figure 3A(i,ii),B(i,ii)), there were no characteristic peaks attributed to biurets in the 1 H NMR spectra (9.1 and 9.4 ppm 54 ), and no characteristic peaks attributed to allophanates in the 13 C NMR spectra (156 ppm 55 ), indicating that these two byproducts were not produced during the synthesis process. The detailed assignment of peaks in NMR spectra can be found in the Supporting Information.…”
Section: 2mentioning
confidence: 99%