A facile method to modify bentonite nanoclay with silane
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Immobilization of smectite clay onto a desirable surface has received much attention, since its nanospace can be utilized for many applications in material science. Here, we present an efficient method to functionalize surface of bentonite nanoclay (BNC) through the grafting of 3-aminotriethoxysilane (APTES). Infrared spectroscopy and elemental analysis confirmed the presence of organic chains and amine groups in modified nanoclay. XRD analysis confirmed grafting of APTES on the surface of bentonite nanoclay without intercalation. The accomplishment of the surface modification was quantitatively proved by TGA analysis. Modified BNC can covalently couple with different material surfaces, allowing its nanospace to be utilized for intercalation of cations, bio-molecules, and polymeric materials, to be used in advanced military aerospace, pharmaceuticals, and many other commercial applications.
KeywordsBentonite nanoclay Covalent modification Nanospace Silane Surface Spectroscopy
The space in between two layers of smectite clay is in nanometer scale, which is potentially suitable for the accommodation of a range of guest molecules. This nanospace in smectite clay plays an important role in different fields such as polymer nanocomposites, cation adsorption, intercalation, and exfoliation [1, 2, 3]. Smectite clay has also shown the ability to release intercalated molecules as and when required . It would be noteworthy if smectite clay can be grafted on different surfaces, while its nanospace is accommodated for special requirements such as targeted drug delivery, disintegrated agents in drug formation, selective removal of heavy metal contaminants, applications in high-temperature environments, and conducting polymers in wearable electronics. In grafting of clay, chemical bonding is more stable and durable compared to physical bonding.
Silane can be used to graft clay particles onto a range of material surfaces [5, 6]. The hydroxyl groups in clay provide excellent sites for silane grafting. Hydroxyl groups in broken edges of clay particles play a vital role in grafting compared to hydroxyl groups in basal surfaces of clay . Hydrolyzed silane can readily form siloxane bonds with hydroxyl groups in basal surfaces and “broken” edges of swelling clay minerals such as montmorillonite and bentonite. In unrestrained conditions, silane can also be physically adsorbed or intercalated with clay. Some X-ray powder diffraction (XRD) data in the literature show an expansion of nanospace in clay due to intercalation of silane [7, 8]. Silane is very reactive with moisture in the air. When silane is exposed to moisture, hydrolysis occurs rapidly, forming self-condensed, water insoluble resinous oligomer, and polymer structures. This has led to conduct silylation in anhydrous organic solvents in inert gas environments. The rates of both silane hydrolysis and condensation are influenced by variations in pH levels. However, the optimum pH for hydrolysis is not optimum for condensation. Finding the best balance between hydrolysis and condensation is one of the keys to the successful grafting of silane.
In a carefully controlled environment, silane-grafted clay compounds contain special functional groups such as –NH2 and –SH, which can be covalently bonded with desirable surfaces . Here, we report a simple one-pot reaction of a silane-grafted BNC compound, which contains –NH2 for further immobilization on various surfaces. In this study, surface characterization, expansion of nanospace of BNC, and bond formation between APTES and BNC were studied.
Materials and methods
A dispersion of BNC was obtained by dissolving 4 g of nanoclay, hydrophilic bentonite nanoclay (Aldrich), in 100 ml of deionized water. Particles of BNC, 100 nm in size, were obtained by ball milling (FRITSCH PULVERISETTE 7 premium line grinder). 2 mmol dm−3 of APTES solution was prepared by controlled dropwise addition of APTES (Aldrich 99%) to deionized water. A precipitation was obtained by 1 ml/min drop rate addition of BNC to APTES solution without agitation in an ambient environment. The slurry was immediately centrifuged (Sigma 3–18) at 9000 rpm for 15 min and washed five times with deionized water. The collected solid was finally dried at 110 °C for 6 h. Modified and non-modified samples were characterized by Fourier transform infrared spectrophotometry (FTIR), XRD, thermogravimetry (TG), and scanning electron microscopy (SEM). XRD profiles were recorded on a Bruker PW 1050 diffractometer using Cu-Kα radiation (λ = 0.154 nm), over a 2θ range of 3°–70°, step size of 0.01, and a step time of 2 s. FTIR spectra were obtained on a Bruker Vertex 80 coupled with Ram-FT module (RAM II, DTGS detector, 4000–400 cm−1 spectral range, resolution of 4 cm−1, OPUS software). TGA was carried out on an SDT Q600 thermoanalyser (TA Instrument, sample mass ~10 mg; heating rate 10 °C/min; nitrogen flow). SEM and energy dispersive X-ray spectroscopy (EDX) analysis were recorded using HITACHI SU6600 microscope coupled with EDX detector.
Results and discussion
The above characterization methods were performed to investigate the expansion of nanospace, covalent bonding, and surface morphology of APTES-grafted BNC.
Bentonite clay in nanoscale increases the hydroxyl groups on the broken edges of its surface, facilitating a rapid silylation. Dropwise addition of APTES to deionized water reduces the ability to polymerize the resulted uncondensed aminopropyl-functional silanetriol monomer. Hence, these uncondensed silanols lead to react with hydroxyl groups on the surface of BNC, forming a stable Si–O–Si bond on drying. When a short time is given for the reaction in low concentration of APTES, grafting mainly occurs on the broken edges of BNC. When stirring and increasing the reaction time, grafting reaction occurs not only on the edge but also on the interlayer nanospace .
Furthermore, delayering of clay can occur under low pH levels. Adjustment of pH was unnecessary, since the alkaline medium created by APTES catalyzed the silane-grafting process, which was an added advantage in silylation of BNC with APTES.
Successfully grafted APTES on BNC can be confirmed by a group of absorption bands in 3000–2800 cm−1 in spectrum (c) (Fig. 2). This absorption is attributed to the valence vibration ν s,as (CH) of propyl chain in APTES. Its presence is also confirmed by a group of bands of weak intensity in 1490–1300 cm−1 region. Spectra (a) and (c) present the same set of absorption bands relevant to inorganic structure of clay . Since modified and non-modified BNC contain water, there is a characteristic absorption band of deformation vibrations of H2O molecules at 1630 cm−1 and a broad intense absorption band above 3420 cm−1 due to vibrations of OH− groups in water molecules participating in the formation of hydrogen bonds. In spectra (a) and (c), the strong broad band in 1100–900 cm−1 is attributed to valence vibration of Si–O bonds in BNC. Moreover, peaks at 3300, 700, and 1340 cm−1 correspond to the N–H stretching, C–H-bending vibrations, and Si–C stretching, respectively. These peaks support the covalent bonding of APTES onto nanoclay. In spectrum (c), intensive bands in approximately 1200–1100 cm−1 represent the asymmetric stretching of siloxane groups (Si–O–Si). These bands correspond to a combination of Si–O–Si vibrational modes including those of bonds formed between the silane and clay surface and cross-linking between silane molecules on the surface .
APTES-grafted BNC has been obtained by a rapid one-pot reaction under mild conditions. XRD data confirmed grafting APTES on broken edges of BNC, without intercalation. FTIR and TGA confirmed covalent modification of APTES on BNC. Furthermore, SEM–EDX investigation proved the presence of elements in APTES-grafted BNC. This appears as a convenient green modification route to produce APTES-grafted BNC, facilitating several applications such as nanoclay vehicles for targeted drug delivery, selective removal of heavy metal contaminants, and intercalation of conducting polymers in wearable electronics.
This work was financially supported by a short-term research grant—Institute of Technology, University of Moratuwa, Sri Lanka, 2016. We would also like to thank Sri Lanka Institute of Nanotechnology (Pvt) Ltd (SLINTEC) for providing facilities for the research.
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