Synthesis and characterization of various surfactants for stabilized CuO powder

Abstract

In the present work, CuO nanoparticles were successfully prepared by the coprecipitation method using copper acetate (Cu(CH3COO)2) as a basic precursor, sodium hydroxide (NaOH) as a precipitator material, sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) as anionic and cationic surfactants, respectively. The synthesized powders samples were characterized by Fourier transform infrared spectrometry (FTIR), field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD). The investigation showed that the added types of surfactants have effects on the decrease of the crystallite size, on the CuO particles morphology, shape and uniform distribution as it is noticed in the XRD and SEM characterizations. Additionally, the FTIR spectra for all the powders samples showed the same Cu-O stretching vibration mode which indicates the presence of a crystalline CuO monoclinic structure. The obtained results create premises for further advanced the applications of CuO powders in various domains. Introduction Over the years, the interests in developing nanoparticles metal oxides have considerably increased due to the necessity of obtaining materials with outstanding physical and chemical properties. Various methods of metal oxide synthesis have been know so far, researches continue to development a new approaches with a strict control over nanoparticles morphology, size and composition for several technological applications. Copper oxide (CuO), belonging to the nanomaterials class, which has attracted recent research because of its excellent properties, cost effectiveness and wide spectrum of practical applications (solar and electrochemical cells, gas sensors, field emitters, active catalyst and antimicrobial activity, etc.). Also, CuO as nanostructured oxide being classified as a p-type monoclinically structured semiconductor material with a direct band-gap value of 1.85 eV presents a particular attention. This type of material has a special concern because it extends the use in a board range of applications, such as electronics and optoelectronics, catalysts, sensors and biosensors, chemical sensing devices, nanofluids and field emitters, desinfection, cosmetic pigments, antibacterial agent, etc. [1–4]. In order for this material to exhibit viable properties in the desired field of applicability, it is intended to establish its method of obtaining and its synthesis parameters; there Powder Metallurgy and Advanced Materials – RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 52-60 doi: http://dx.doi.org/10.21741/9781945291999-6 53 have been elaborated and known various physical and chemical methods so far, such as sol-gel, coprecipitation, hydrothermal synthesis, mechanical mixing, solid state reaction, thermal descomposition of precursors, microemulsion, microwave irraditiaon, physical vapor deposition, ablation, etc. [3, 5, 6]. From the bottom-up type methods, precipitation is a cheap one, with applicability on a broadscale, and which does not involve the addition of secondary reaction products [7–9]. Particularly, in order to obtain CuO, the method involves precipitation of various soluble copper salts (nitrates, chlorides, sulphates and acetates) in aqueous solutions, followed by their thermal decomposition with oxide formation [4, 5, 10]. Inorganic salts are mixed in an aqueous medium and under a rigorous pH control by using solutions of NaOH, KOH, (NH4)2CO3 or NH4OH, finally the precipitates obtained are subject to characteristic thermal treatment. In the synthesis process the reaction parameters (pH, rate of addition of reactants and speed of stirring, solution concentration, reaction temperature, etc.) have a determining role in the particle size, morphology and granulometry [11 – 13]. In the literature various thermal treatments at relatively high temperature (between 700 °C and 1100 °C) are presented, leading to the phenomenon of agglomeration and increase of particles average size. To prevent the tendency of agglomeration and to favour the formation of nanostructured materials, the use surfactants have been proposed to be used. The use of different surfactants allows the improvement of particles structural, physico-chemical and morphological properties due to the electrostatic and stearic stabilizing mechanisms that reduce the solutions surface tension and improve the nanocrystalline material properties [6, 14 – 18]. Also, the addition of surfactants in the oxide materials precipitation process leads to increase nanoparticle stability and interaction between surfactant molecules and metal ions. The surfactants are chemical substances, focusing on the surface and solubilized materials with low affinity relative to each other. They have an asymmetrical molecular structure, consisting of a non-polar (hydrocarbon) and a polar (ionisable or non-ionisable) part. The role of surfactants is to provide an effective and efficient coating to induce electrostatic or stearic repulsions that can counterbalance van der Waals attractions [19 – 22]. The specialized literature shows research studies to improve the properties and formation of CuO nanoparticles by using various surfactants of the type of of oleic acid (OA), polyethylene glycol (PEG), cetyltrimethylammonium bromide (CTAB), hypochlorite dodecyl sulphate (SDS), polyvinylpyrrolidone (PVP), tetraoctylammonium bromide (TOAB), playing an important role in the synthesis process steps since the incipient phase. The reason for selecting the two types of surfactants (CTAB and SDS) in the experiments carried out in the present study is based on their remarkable effects on particle stability, size changing, morphology and the surface properties of the precipitated particles, but also because they have low price, can be found relatively easy on the market and have low toxicity [7, 14, 23 – 25]. This paper presents the study of obtaining CuO nanoparticles by the coprecipitation method, in the absence and in the presence of two types of surfactants, anionic (SDS) and cationic (CTAB). It is presented the effect of surfactants on CuO nanoparticles morphology, average size and crystalline structure. The morphological and structural properties are highlighted by using field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD) and Fourier transform infrared spectrometry (FT-IR). Powder Metallurgy and Advanced Materials – RoPM&AM 2017 Materials Research Forum LLC Materials Research Proceedings 8 (2018) 52-60 doi: http://dx.doi.org/10.21741/9781945291999-6 54 Experimental details For the synthesis of CuO powders: copper acetate monohydrate [Cu(CH3COO)2], sodium hydroxide [NaOH] and surfactants of type anionic [C12H25NaO4S, SDS 99%] and [C19H42BrN, CTAB > 99 %], were used as starting materials. All reagents were purchased from the company Sigma-Aldrich without any previous purification. For the synthesis of CuO in the absence and in the presence of surfactants the stock solutions of 1M [Cu(CH3COO)2] and 1M [NaOH] were prepared, respectively. From the stock solution of acetate one part is taken and the pH is adjusted in basic medium by adding NaOH solution in dropwise until the formation of a greenish-blue precipitate was observed. In the case of samples with surfactant, over the source of copper the afferent surfactants (SDS and CTAB concentration 0.1 M) was added and under continuous stirring the precipitating agent (NaOH) was adding in dropwise until the precipitate formed and the pH was adjusted to about 1011. After the precipitation formation, the stirring continues up to a temperature of 80 °C. The introduction of SDS anionic surfactant induces a homogeneous nuclear process due to considerable size effect of counter-ions on the crystal facets. By adding CTAB as a cationic surfactant there is a complete ionization and cation formation in the tetrahedric structure, but it also determines a control of the growth rates of different faces of the CuO nanoparticles [14, 26]. For all synthesized samples the same synthetic conditions (time, temperature and pH) were maintained. The precipitates thus formed are left in the rest position, then have been filtered under vacuum using a Buchner funnel, and following they were washed with a water-ethanol mixture for purification and removal of the secondary compounds. After washing, the samples were subjected to the drying step in the oven at a temperature of 80 °C, preceded by calcination sintering at a temperature of 550 °C for 3 hours in normal atmosphere. Due to the sintering temperature of the dry samples changed colour from green to blue to black. The functional groups and the chemical bonds of the synthesized oxide samples were analyzed by Fourier Transform Infrared spectrometry (Bruker Optics, Vertex 80V) using the KBr pellet method in the wavenumber range of 4000-400 cm by averaging 64 scans. In the processing of all spectra, the bands attributable to the vibration mode of the C=O bond in CO2 were extracted. In order to investigate the morphology and particle size a Field Emission Scanning electron microscope (FE-SEM), obtained at an operating voltage at 10 kV and a magnitude of 30 000x has been used. X-ray diffraction measurements of the synthesized CuO particles were recorded using a Rigaku Smartlab diffractometer with the radiation CuKa=1.540593 Å, indicating the limit of variation for the current between 150 mA and 190 mA. Data were collected at a scan rate of 12°/min. in the range 20 = 20-95°. Results and Discussion FTIR Spectra The FTIR spectra of the different samples are presented as a comparison between CuO powders obtained in the absence of surfactants (Figure 1a) and in the presence of surfactants (Fig. 1b and c). For all samples treated at 550 °C, bands attributed to both the vibration mode of the Cu-O linkages in the precursor and to the surfactants vibration mode can be seen, thus suggesting the binding of surfactants to particle surface. Band