Morphological changes of gel-type functional polymers after intermatrix synthesis of polymer stabilized silver nanoparticles
© Bastos-Arrieta et al.; licensee Springer. 2013
Received: 15 November 2012
Accepted: 20 April 2013
Published: 29 May 2013
This paper reports the results of intermatrix synthesis (IMS) of silver metal nanoparticles (Ag-MNPs) in Purolite C100E sulfonic ion exchange polymer of the gel-type structure. It has been shown that the surface morphology of the initial MNP-free polymer is absolutely smooth, but it dramatically changes after the kinetic loading of Ag on the polymer and then IMS of Ag-MNPs. These morphological changes can be explained by the interaction of Ag-NPs with the polymer chains, leading to a sort of additional cross-linking of the polymer. As a result, the modification of the gel-type matrix with Ag-MNPs leads to the increase of the matrix cross-linking, which results in the increase of its surface area and the appearance of nanoporosity in the polymer gel. Ag-MNPs are located near the polymer surface and do not form any visible agglomerations. All these features of the nanocomposites obtained are important for their practical applications in catalysis, sensor applications, and bactericide water treatment.
Ion exchange materials find numerous large-scale industrial applications in various fields, such as water treatment processes, catalysis, and some others. The efficiency of the use of ion exchangers in some instances can be substantially improved by tailored modification of commercially available ion exchange materials with, for example, functional metal nanoparticles (FMNPs) .
The modification of ion exchangers with FMNPs can be carried out by using the intermatrix synthesis (IMS) technique coupled with the Donnan exclusion effect. Such combination allows for production of polymer-metal nanocomposites with the distribution of FMNPs near the surface of the polymer on what appears to be the most favorable in their practical applications. This technique has been used to modify the polymers with cation exchange functionality with FMNPs by using the procedure described by the following sequential stages: (1) immobilization (sorption) of metal or metal complex ions (FMNP precursors) onto the functional groups of the polymer and (2) their chemical or electrochemical reduction inside the polymer matrix (IMS stage) [2–7].
The use of the functional polymers as supports for the metal nanoparticles (MNPs) and metal oxide nanoparticles has, in this sense, one more important advantage dealing with the possibility to synthesize the FMNPs directly at the ‘point of use’ , i.e., inside the supporting polymer, which results in turn in the formation of the polymer-metal nanocomposites (PMNCs) with desired functionality [8–11].
Ag, due to its antibacterial features, represents one of the hot topics of investigation in the noble metal research. The unusual properties of nanometric scale materials in comparison with those of their macro counterparts give in many instances a number of advantages in their practical applications [12–14]. In fact, Ag-MNPs are widely used due to their more efficient antimicrobial activity in comparison with bulk silver . Some of our previous studies were dealt with the IMS of Ag-NPs in different polymer matrices and application of resulting PMNCs for bactericide water treatment [2, 3]. Essentially, in all publications dedicated to the synthesis and application of Ag-MNPs in various supporting polymers, the main attention was paid to the properties of MNPs, i.e., to the properties of just one component of PMNCs, which are determined by PMNC components: the polymer matrix, the NPs, as well as the interaction between them.
In this communication, we report the results obtained by studying the properties of the polymer component of FMNPs composed of Ag-MNPs and Purolite C100E resin of the gel type. It has been shown that IMS of Ag-MNPs in a gel-type polymer results in the dramatic changes of its morphology.
Reagents and materials
All chemicals, such as AgNO3, NaOH (Panreac, S.A., Barcelona, Spain), NaBH4 (Aldrich, Munich, Germany), mineral acids, and others, were of p.a. grade and were used as received. Bidistilled water was used in all experiments. The ion exchange capacity of C100E resin (Purolite, Bala Cynwyd, PA, USA) was determined by acid-base titration to equal to 2.1 meq g−1.
Synthesis and characterization of PMNCs
The IMS of Ag-NPs in Purolite C100E resin was carried by following the standard procedure which included the loading of the functional groups of the polymer in the initial Na form with Ag+ ions by using 0.1 M AgNO3 solution followed by their reduction with NaBH4 solution.
A sample of approximately 10 mg of PMNC was immersed in aqua regia (1 mL) to completely dissolve Ag-MNPs. The final solution was filtered through a 0.22 μm Millipore filter (Millipore Co., Billerica, MA, USA) and diluted for quantification of metal content by using induced coupled plasma optical emission spectrometry (Iris Intrepid II XSP spectrometer, Thermo Electron Co., Waltham, MA, USA) and ICP-MS (Agilent 7500, Agilent Technologies, Inc., Santa Clara, CA, USA). The average uncertainty of metal ion determination was less than 2% in all cases. The specific surface area and the porosity measurements were carried out by using BET technique on Micromeritics ASAP-2000 equipment (Micromeritics Instrument Co., Norcross, GA, USA).
Scanning electron microscope (SEM) coupled with an energy-dispersive spectrometer (EDS) (Zeiss EVO MA 10 and Zeiss MERLIN FE-SEM, Carl Zeiss AG, Oberkochen, Germany) and transmission electron microscope (TEM) studies were carried out using JEOL 2011 and JEOL 1400 (JEOL Ltd., Akishima, Tokyo, Japan). SEM and TEM techniques were used to obtain the metal concentration profiles across the cross section of the FMNP-containing materials, to characterize the morphology of the polymer surface, and for determination of MNP diameters. The PMNC samples were prepared by embedding several granules in the epoxy resin followed by cutting with an ultramicrotome (Leica EM UC6, Leica Microsystems Ltd., Milton Keynes, UK) using a 35° diamond knife (Diatome, Hatfield, PA, USA) at liquid nitrogen temperature (−160°C).
Results and discussion
Increase of pore diameters in Ag-MNP-containing Purolite C100E resin samples
Ag-MNP content (mg/g)
BET average pore diameter (nm)
Ag-C100E PMNC (5a)
112.7 ± 0.5
2.3 ± 0.2
Ag-C100E PMNC (10a)
143.5 ± 0.5
4.4 ± 0.2
The dramatic changes in morphology of the polymer surface are caused by a strong interaction of Ag-MNPs with the polymer matrix. These morphological changes are associated with the inter-polymer mechanical stress, resulting from a strong interaction between Ag-MNPs and the polymer chains. The changes observed must substantially improve the mass transfer properties of the Purolite® C100E resin in comparison with the initial (MNP-free) polymer due to the appearance of nanoporosity (see Figure 3 and Table 1).
IMS technique coupled with the DEE can be successfully applied for the modification of polymers with FMNPs. This version of IMS results in the situation of FMNPs onto the surface of the obtained nanocomposite materials, providing the most favorable distribution that substantially enhances their practical applications. In addition, the DEE-IMS of Ag-MNPs inside the polymeric matrix results in dramatic changes of their morphology, where the most remarkable changes are observed in the case of gel-type polymers (such as Purolite C100E).
The appearance of Ag-MNP-induced porosity results in the formation of a nanoporous nanocomposite material with enhanced mass transfer characteristics, which in turn, must improve the performance of corresponding sensors and biosensors based upon these novel materials as well as the bactericide assays. It seems important to emphasize that the nanoporosity simultaneously appears in C100E resin in the course of the polymer loading with Ag-MNPs.
The authors are sincerely grateful to all their associates cited throughout the text for making this publication possible. Part of this work was supported by the research grant MAT2006-03745, 2006-2009 from the Ministry of Science and Technology of Spain, which is also acknowledged for the financial support of DN.M. JB also thanks the Autonomous University of Barcelona for the personal grant.
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