2016
DOI: 10.1002/app.44245
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Functionalization of carbon nanotubes with (3‐glycidyloxypropyl)‐trimethoxysilane: Effect of wrapping on epoxy matrix nanocomposites

Abstract: In this work, multiwalled carbon nanotubes (MWCNT), after previous oxidation, are functionalized with excess (3‐glycidyloxypropyl)trimethoxysilane (GLYMO) and used as reinforcement in epoxy matrix nanocomposites. Infrared, Raman, and energy‐dispersive X‐ray spectroscopies confirm the silanization of the MWCNT, while transmission electron microscopy images show that oxidized nanotubes presented less entanglement than pristine and silanized MWCNT. Thickening of the nanotubes is also observed after silanization, … Show more

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Cited by 12 publications
(10 citation statements)
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“…This enrichment in flexural strength upon addition of FCNTs can be attributed to these two facts (a) the stronger interfacial bond between CNT and epoxy due to the chemical linkage of functional group with both of them and (b) improved state of dispersion due to polar nature of FCNT preventing intermolecular interaction . In case of UCNT, the interfacial bonding is primarily due to the weak Van der Waal kind physical interactions between CNT and epoxy.…”
Section: Resultsmentioning
confidence: 99%
“…This enrichment in flexural strength upon addition of FCNTs can be attributed to these two facts (a) the stronger interfacial bond between CNT and epoxy due to the chemical linkage of functional group with both of them and (b) improved state of dispersion due to polar nature of FCNT preventing intermolecular interaction . In case of UCNT, the interfacial bonding is primarily due to the weak Van der Waal kind physical interactions between CNT and epoxy.…”
Section: Resultsmentioning
confidence: 99%
“…The bands at 2989∼2843 cm −1 corresponding to the C-H [28] vibrations shown in Fig.9 (e) demonstrate, that all four polar silanes are grafted onto the silica surface. The intensive C-H stretching band in Fig.9 (e) indicates the presence of the epoxy silane on the silica surface due to the high number of CH 2 units in the chemical structure of this silane, although the bands from the epoxy ring group were not detected [29]. The broad band around 1631 cm −1 visible in Fig.9 (f) and assigned to N-H stretching belongs to the amine group of the amino silane [28].…”
Section: ) Fourier-transform Infrared Spectroscopy (Ftir)mentioning
confidence: 97%
“…[34][35][36]38,39 In addition, it is observed that the amorphous carbon reflected by the D band is prominent, which means a high defect level. 40 To evaluate the disorder of GHN, the ratio of the D to G peak intensities (I D /I G ) is calculated (∼1.1), suggesting the partial amorphous nature of GHN resulting from its oxidation. 41 It was reported that during the oxidation reaction, disordered sp 3 -oxidized domains with various oxygen functional groups (such as epoxides, ketones, hydroxyls, carboxylic acids, and so forth) could surround the sp 2 graphitic domains.…”
Section: Resultsmentioning
confidence: 99%