1986
DOI: 10.1016/0021-9797(86)90275-4
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FT—IR characterization of the reaction at the silane/matrix resin interphase of composite materials

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Cited by 96 publications
(56 citation statements)
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“…Different techniques were applied: transmission on thin films or pellets [5][6][7] (KBr, NaCl), diffuse reflectance infrared spectroscopy 6,7) (DRIFT), reflection-absorption infrared spectroscopy 8,9) (RAIR) or the attenuated total reflection (ATR) spectroscopy [10][11][12][13] . Different methods for modifying silicon substrates and glass fibers to get amino-functionalized surfaces are described as well 1,2,5,6,8,14,15) . Culler et al 14) studied the chemical reaction between c-APS films and epoxy resin films.…”
Section: Introductionmentioning
confidence: 99%
“…Different techniques were applied: transmission on thin films or pellets [5][6][7] (KBr, NaCl), diffuse reflectance infrared spectroscopy 6,7) (DRIFT), reflection-absorption infrared spectroscopy 8,9) (RAIR) or the attenuated total reflection (ATR) spectroscopy [10][11][12][13] . Different methods for modifying silicon substrates and glass fibers to get amino-functionalized surfaces are described as well 1,2,5,6,8,14,15) . Culler et al 14) studied the chemical reaction between c-APS films and epoxy resin films.…”
Section: Introductionmentioning
confidence: 99%
“…It is appropriate to determine this working window for a given purpose rather than to rely on literature because different silanes display different reaction rates and because the influence of the (uncontrolled) presence of impurities cannot be underestimated [33,34]. The extent of silane hydrolysis can be monitored by 1 H NMR, while that of condensation can be monitored by 29 Si NMR.…”
Section: Optimisation Of the Silane Solutionmentioning
confidence: 99%
“…Nuclear magnetic resonance spectroscopy (NMR) 1 H NMR measurements were performed on a Bruker 400 Advance at room temperature, averaging 8 scans with a spectral width of 20.62 ppm and an acquisition time of 1.99 s. Chemical shifts were referenced to the water-hydrogen peak at 4.79 ppm and time between sample preparation and the first measurement was kept as low as possible: i.e. between 165 s and 180 s. 29 Si NMR measurements were done using a Bruker 600 Advance at room temperature, averaging at least 256 scans with a spectral width of 5031.70 ppm and an acquisition time of 0.55 s. Recording 1 spectrum takes at least 2 h, and when discussing results, the time associated with a given measurement refers at the time lapse between preparation of a given solution and finishing of the measurement. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX)-SEM analysis was performed with a JEOL JSM-7000F Field Emission Gun scanning electron microscope with high spatial resolution operated at a 20 kV accelerating voltage.…”
Section: Analysis Techniquesmentioning
confidence: 99%
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“…Este agente de acoplamiento (γ-APS) ha sido ampliamente estudiado en materiales compuestos de matriz orgánica reforzados con fibras (19)(20)(21)(22).…”
Section: Introductionunclassified