2019
DOI: 10.1007/s10973-019-08793-6
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Rheokinetic characterization of polyurethane formation in a highly filled composite solid propellant

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Cited by 20 publications
(12 citation statements)
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“…FT-IR spectroscopy was utilized to quantify the extent of HTPB reaction with IPDI to polyurethane [117,118]. The relative ratio of absorbance of the FT-IR bands at 1710 cm À 1 (À C=O stretching of urethane) with that of the peak at 966 cm À 1 [À C=C-(trans) vibration of HTPB], i. e., A 1710 /A 966 was compared, and the extent of urethane content was calculated [119,130]. FT-IR was used in combination with NMR [131].…”
Section: Infrared Spectroscopy (Ft-ir)mentioning
confidence: 99%
“…FT-IR spectroscopy was utilized to quantify the extent of HTPB reaction with IPDI to polyurethane [117,118]. The relative ratio of absorbance of the FT-IR bands at 1710 cm À 1 (À C=O stretching of urethane) with that of the peak at 966 cm À 1 [À C=C-(trans) vibration of HTPB], i. e., A 1710 /A 966 was compared, and the extent of urethane content was calculated [119,130]. FT-IR was used in combination with NMR [131].…”
Section: Infrared Spectroscopy (Ft-ir)mentioning
confidence: 99%
“…Many methods are employed to the PU polymerization kinetics, broadly classi ed into two groups: (i) indirect methods, which measure a physical property functionally related to the extent of the reaction, such as differential scanning calorimetry (DSC), rheometry and viscometry; (ii) direct methods, which measure the concentration of a reactant or product species, such as Fourier transform infrared spectroscopy (FTIR), titration, nuclear magnetic resonance (NMR) and gel permeation chromatography (GPC) [9][10][11][12]. Nevertheless, the very high viscosity and fast gel formation observed when the urethane conversion reaches a signi cant level brings analytical problems to direct methods, limiting their use [15] .…”
Section: Introductionmentioning
confidence: 99%
“…Activation energy values for the polymerization are in the 45 − 55 kJ/mol range [18,19], considered an autocatalytic reaction mechanism [12], in which the monomer acts as a catalyst for the reaction, increasing the conversion rate. The most used autocatalytic models in these studies were Prout-Tompkins and Kamal-Sourour [14,16].…”
Section: Introductionmentioning
confidence: 99%
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