Facile Solventless Synthesis of a Nylon-6,6/Silver Nanoparticles Composite and Its XPS Study

Silver nanoparticles were synthesized and supported on thin nylon membranes by means of a simple method of impregnation and chemical reduction of Ag ions at ambient conditions. Particles of less than 10 nm were obtained using this methodology, in which the nylon fibers behave as constrained nanoreactors. Pores on nylon fibres along with oxygen and nitrogen from amide moieties in nylon provide effective sites for in situ reduction of silver ions and for the formation and stabilization of Ag nanoparticles. Transmission electron microscopy (TEM) analysis showed that silver nanoparticles are well dispersed throughout the nylon fibers. Furthermore, an interaction between nitrogen of amides moieties of nylon-6,6 and silver nanoparticles has been found by X-ray photoelectron spectroscopy (XPS).


Introduction
Research on the synthesis of mesoporous materials containing nanoparticles represents a fast-developing area of nanoscience and nanotechnology.This interest is stimulated by several possible application areas of these materials including catalytic [1], magnetic [2], and optoelectronic [3,4].Metal nanoparticles dispersed in polymeric matrixes have recently been the subject of intense study aiming to develop nanocomposite films [5][6][7][8].General approaches for the synthesis and support of nanoparticles inside porous materials include impregnation [9] and deposition-precipitation [10].A drawback of this nanocomposites is the difficulty to disperse nanoparticles in most systems [11]; hence one potential advantage of such metal/polymer systems is that the size and distribution of dispersed metal nanoparticles can be readily controlled based on the properties of the host polymer [12,13].
Silver particles with a narrow size distribution have been produced upon reversible chemical transformation between metallic and oxide states in a titania matrix [14] and in a mesoporous silica which was grafted with hydrophobic -Si(CH 3 ) 3 groups at the pore surface [15].
Nylon is an electron-rich and polar synthetic polymer (polyamide) usually made from the monomers adipoyl chloride and hexamethylene diamine to form a linear molecular chain (Figure 1).Synthetic nylon membranes have a porous structure [16] and are composed of microfibrils that are interconnected forming a three-dimensional network.Such morphological features provide a unique reaction vessel for synthesizing and supporting metal nanoparticles, allowing enhanced access of guest molecules to catalytic centres, compared with nonporous films.
In this work, a facile synthesis of silver nanoparticles of less than 10 nm in diameter with a narrow size distribution, using porous nylon fibers as unique nanoreactors to generate a nylon-6,6/silver nanoparticles composite, is reported.

Experimental
All chemical reagents were analytical grade and were used without further purification.The measurements of lattice-fringe spacing and angles were made using digital image analysis of reciprocal space parameters, according to Akamatsu et al. [17].Using this method the precision is 0.0001 nm for lattice spacing and 0.1 ∘ for lattice plane angles.This analysis was carried out with the Digital Micrograph software, Oxford, UK.

Preparation of the
X-ray photoelectron spectroscopy (XPS) was performed using an UHV system of VG Microtech ESCA3000 Multilab, with an Al K  X-ray source (1486.6 eV) and CLAM4MCD analyser.The surface of the sample was etched for 10 s with 3 kV Ar + at 0.16 A/mm 2 .The XPS spectrum was obtained at 55 ∘ from the normal surface in the constant pass energy mode; the pass energies used were 50 eV and 20 eV for survey and high resolution, respectively.The peak positions were referenced to the Shirley background Ag 3d 5/2 photopeak at 368.21 eV and C 1s hydrocarbon groups in a binding energy of 285.00 eV.XPS spectra were fitted with the program SDP v 4.1 [18].For the process of deconvolution the uncertainty in the binding energy was estimated to be 5% (i.e., ±0.05 eV).

Results and Discussion
The membranes used in this work are composed of nylon-6,6 fibers in the micrometer range, as shown in Figure 2(a).The fibers surface is rough (Figure 2(b)) and has several pores of less than 100 nm in diameter (inset Figure 2(b)).
These pores may allow guest molecules to enter.Thus, when a nylon membrane is immersed in aqueous AgNO 3 , Ag + ions are readily impregnated into the nylon membrane fibers through the pores.Most of the incorporated Ag + ions are bound to nylon macromolecules probably via electrostatic (i.e., ion-dipole) interactions, because the electron-rich oxygen and nitrogen atoms of polar amides groups are expected to interact with positive metal ions.The posterior rinse with ethanol (ca.30 s) removes Ag + ions that were not anchored to nylon fibres.Figure 3 shows the pure nylon membrane and nylon membranes having Ag nanoparticles, using 0.5 mM, 1 mM, 1.5 mM, and 10 mM AgNO 3 solutions, respectively.As the concentration of nanoparticles increases, the membranes exhibit different colours from light yellow to yellow and finally yellow-brownish.
Energy-dispersive X-ray spectroscopy (EDX) spectrum in Figure 4, which was collected from the nylon-6,6/silver nanoparticles composite, clearly shows the presence of Ag signal peak, indicating the effectiveness of the electrostatic assembly of the particles on the surface of the nylon fibers.The yellowish colour of Ag-nylon composite membrane (Figure 3) also suggests the presence of Ag nanoparticles on the polymer surface.
UV-Vis spectra of the nylon-6,6/silver nanoparticles composites are shown in Figure 5.Because the nylon-6,6 membrane was used as the reference, the absorption spectra can be considered as the absorption of Ag species.Using 0.5 mM AgNO 3 a narrow symmetrical absorption band is   located at 390 nm (Figure 5(a)); this is attributable to the surface plasmon resonance of silver nanoparticles in agreement with the observed yellow colour showed in Figure 3 [19].No absorption was observed at wavelengths longer than 450 nm.These observations imply that Ag nanoparticles were formed.The surface plasmon peak underwent a shift to It is noted that the absorption intensity of the plasmon band increases as the concentration of aqueous AgNO 3 augments, also in agreement with the membrane intensity changes in colour, which can be attributed to the increase in the Ag nanoparticles concentration.These assumptions are confirmed by TEM observations.As shown in Figure 6 monodisperse Ag nanoparticles were obtained at AgNO 3 0.5 mM.Their mean diameter (d) was measured as 3.3 nm with a standard deviation () of 0.9 nm.
Figure 7 shows Z-contrast images of nylon fibres with Ag particles.Figures 7(a) and 7(c) correspond to a concentration of 1.0 mM of AgNO 3 resulting in nanoparticles with an average size of 4.3 nm with a standard deviation of 1.4 nm.Using a solution of 1.5 mM AgNO 3 (Figures 7(b) and 7(d)), the average particle size slightly increases to 6.2 nm with a standard deviation of 1.8 nm.Therefore, it is possible to control the size and size distribution by adjusting the concentration of metal ions in solution.
Because of the porous structure of nylon fibre and the strong interactions between Ag + ions and the carbonyl and amide groups of nylon macromolecule, Ag + ions were uniformly and tightly anchored to the nylon fibres [20].Such interactions would lower the mobility of Ag + ions, enhance the formation of silver nuclei, limit the formation of several morphologies, and prevent the growth of larger particles [21].This is particularly true at low Ag + ion concentrations and can explain the formation of monodisperse Ag nanoparticles (after NaBH 4 reduction) under such conditions.At higher AgNO 3 concentrations, larger amounts of Ag + ions are embedded on nylon membranes, leading to large and widely distributed particles after reduction [22].In these kinds of systems, it is expected that the carbonyl and amide groups may also play an important role in stabilization of metal nanoparticles in addition to the porous structure of nylon fibres.
The HRTEM image in Figure 8 shows Ag nanoparticles between 2 and 3 nm in diameter.This image possesses atomic resolution; therefore, several crystalline planes are distinguishable and the interplanar distances can be measured.The interplanar distances shown in the micrograph were measured from the Fourier transforms (FFT) of these nanoparticles (Figure 8, bottom), where the corresponding crystalline planes are specified.The interplanar distances and their corresponding crystalline planes match the ones of metallic Ag (FCC) phase.The measured interplanar distance is 2.36 Å and corresponds to the (111) plane [23].
In order to examine the chemical composition of the nylon-6,6/Ag nanoparticles fibre composite, as well as the possible interaction of silver metal with the nylon moieties, after formation of Ag nanoparticles, X-ray photoelectronic spectroscopy (XPS) was used.Figure 9 shows the XPS survey spectra obtained after Ar + etching for 10 s.
Figure 9 shows the increase in the Ag 3d signal corresponding to the different concentrations of AgNO 3 added in the solution reaction; a spectrum of nylon-6,6 is used as reference.Clearly an increase of the concentration of the metal precursor salt favours the formation of the nylon/ Ag composite.
In order to obtain more information about the chemical state of the Ag nanoparticles present in the composite a curve fit of the various signals was made and is shown in Figure 10.
Table 1 shows the binding energies of the XPS deconvolution of Ag 3d, C 1s, O 1s, and N 1s core levels samples with the Ag metallic, AgO, and nylon-6,6 as references.The peak energy position in the deconvolution and number of peaks were based in data reported by Beamson and Brigs [24] and Hoflund and Hazos [25] and calibrated with metallic Ag foil as reference.
From Table 1, a positive chemical shift in N 1s core level and negative chemical shift in Ag 3d 5/2 of Ag(0) of nanoparticles, with respect to N 1s and Ag 3d 5/2 of nylon and Ag metallic, are observed.From the data in Table 1 the general rule based on the electronegativity can explain both the positive chemical shift of the N 1s core level and the negative chemical shift of the Ag 3d 5/2 core level.This effect can be seen It can be also observed that for N 1s the maximum shifting (Δ) occurs for the 0.5 mM simple with Δ = 0.22 eV; however, for 0.1 mM sample, Δ = 0.11, it contains the largest amount of Ag nanoparticles, taking in account the amount of AgO.For the 1.5 mM sample, Ag 3d peaks can be deconvoluted satisfactorily obtaining thus all oxidation states even in the samples with less Ag concentration.In addition, in Figure 10, the data obtained from the curve fitting show that there is no change in the binding energy of the orbitals of C 1s despite the use of different AgNO 3 concentrations.There is, however, a 0.31 eV shift in the N 1s peak corresponding to the sample with 1.5 mM AgNO 3 .This small shift in binding energy suggests there is an interaction of the nitrogen atoms in nylon during the stabilization of the silver nanoparticles.
A similar chemical shift for N 1s binding energy in XPS spectra has been observed for the interactions of PVP with Pt nanoparticles and nitrocellulose with Ru [26,27].Hence, pores of nylon fibers, where the nitrogen atoms from the amide groups are found, not only interact with the metal ions presumably through iondipole forces, but once the reduction reaction occurs, they also stabilize the Ag nanoparticles.Analysis of the O 1s and Ag 3d 5/2 peaks shows the presence of AgO, which was expected due to the high reactivity of the silver nanoparticles at the sizes obtained.Nevertheless, the fact that there is still a signal corresponding to Ag 0 suggests that the oxidation takes place only on the surface of the nanoparticles, while metallic silver remains at their core; again this is possible due to the stabilizing effect of the amide groups present in the nylon fibers.This nylon-6,6/Ag nanoparticles composite will be probed in dyes removal from aqueous solutions and in applications regarding its antibacterial properties.

Conclusions
It was demonstrated that using an aqueous Ag ion impregnation of nylon fibres followed by a reduction with NaBH 4 , a composite of Ag nanoparticles attached to the polymer can be formed.The whole process is carried out at ambient conditions.SEM, HRTEM, and XPS studies confirmed the presence of such Ag nanoparticles in the fibres, with an average size of 3.3 nm.This very simple and versatile synthetic route could be applied to obtain other composites made of metal nanoparticles and natural or synthetic polymer fibres.Moreover, an interaction between nitrogen of amides moieties of nylon-6,6 and silver nanoparticles has been found by X-ray photoelectron spectroscopy.

Table 1 :
The binding energy position by XPS of nylon-6,6-and Ag-containing samples core levels Ag 3d, C 1s, O 1s, and N 1s.
in Figure10for N 1s.For the composite samples analysed, all C 1s, O 1s, and Ag 3d 5/2 of AgO core levels are in the same positions as exhibited in Table 1 and Figure 10.O 1s (530.33 eV) corresponds to O=C and Ag-O at 367.31 eV; C 1s corresponds to (1) C-CH 2 at 283.84 eV, (2) CH 2 -CH 2 at 284.14 eV, (3) CH 2 -N at 285 eV, and (4) C=O at 286.81 eV.