Abstract
The thermal decomposition of cobalt, nickel, manganese, zinc, and copper nitrates supported on nanometric alumina was investigated and compared with decomposition of corresponding bulk nitrates. TG, DTA, and MS measurements in air were performed. The supported nitrates decompose in lower temperatures than the bulk ones and their decomposition proceeds in fewer stages which are better separated. Synthesized materials and bulk nitrates before degradation of nitrates groups undergo dehydration. For decomposition of manganese and copper nitrates, the last step of water vapour releasing is combined with degradation of nitrate groups thus formation of anhydrous metal nitrate during decomposition is not achievable. Thermal decomposition of bulk nitrates leads to oxides—Co3O4, NiO, MnO2, ZnO, and CuO—respectively, as the solid residue. The nickel, zinc, copper, and manganese nitrates while supported on alumina decompose to corresponding oxides (NiO, ZnO, CuO, MnO2) as well. For decomposition of cobalt nitrate while supported on Al2O3 as the solid residue CoAl2O4 were identified. The correlation between dehydration and degradation of nitrates groups temperatures for bulk and supported nitrates was analysed in terms of atomic properties of d-metals.
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Introduction
Metal oxide submicrometer particles have received widespread interest recently because of their envisioned applications in electronics, optics, and magnetic storage devices as well as materials for catalytic applications [1, 2]. The properties of metal oxide catalysts, such as specific surface area, phase composition, particle size, porosity, and activity are greatly affected by the conditions chosen for their preparation [3]. The kind of precursor materials, temperature, and duration of heat treatment as well as the composition of surrounding atmosphere are important parameters.
Metal nitrates hydrates are very often used as the precursors of metal oxides because they give materials of well-defined chemical composition and high specific surface area [4–9]. The advantage of nitrates compared to chlorides or sulphates is that they can be fully converted to corresponding oxides. However, conditions for the synthesis of metal oxides having appropriate properties usually have to be found experimentally [10].
The decomposition of d-metal nitrates hydrates proceeds by stages and rarely leads to anhydrous salt. Usually the dehydration process is not complete and the beginning of nitrate(V) groups decomposition occurs simultaneously with hydration water evolution [11–15]. The mechanism of d-metal nitrates hydrates decomposition is rather complicated and proceeds in different ways depending on whether the gas atmosphere is oxidizing, neutral or reducing. The complete decomposition resulting in metal oxide formation is usually finished below 300 °C [16]. In moist atmosphere, the decomposition of d-metal nitrates can occur at lower temperatures than in dry atmosphere [17].
High specific surface area metal oxides can be synthesized by a route involving impregnation of different types of porous materials, like alumina, carbon, clay, zeolite or silica, with concentrated metal salt solutions and subsequent thermal treatment [18, 19]. This route allows the synthesis of a wide variety of different metal oxides, either as defined phases, if suitably chosen amounts of precursor salts are used, or as amorphous or partially crystalline multiple mixed-metal oxides. Typically, specific surface areas in the range between 50 and 200 m2 g−1 are accessible, and in addition to crystalline binary oxides, a number of spinels and perovskites can also be prepared.
The decomposition of supported nitrates can be strongly affected by the nature of the support. Results obtained by Tiernan et al. [20] show that, depending on the properties of support, the decomposition of the supported cobalt nitrate can either be delayed or enhanced. Further, the crystal size of metal nitrates can affect the decomposition. Cseri et al. [21] have reported that the decomposition of metal nitrates supported on a clay was started and was completed at temperatures of 0–40 and 5–105 °C lower, respectively, compared with the bulk metal nitrates. Since the decomposition was shifted to lower temperatures pronouncedly for the most amorphous nitrates, it was concluded that this shift was due to the small crystal size of the nitrates. They also noted that some decomposition steps that were observed during the decomposition of bulk nitrates were not observed for the supported samples. In [22] the authors showed that NiO particles prepared by decomposition of nickel nitrate supported on SBA-15 under the stream of He containing 1 % of NO resulted in the exclusive formation of small particles with a diameter of about 4 nm. Results obtained in [23] revealed that the routes of decomposition of nickel nitrate bulk and supported on alumina are different, especially concerning formation of intermediate phases in the later case.
The literature concerning the decomposition of supported metal nitrates is mainly focused on the properties and possible applications of the final residue—support covered by metal oxides. In this paper, decomposition of chosen d-metal nitrates supported on the nanometric alumina was investigated and compared with decomposition of correspondent bulk nitrates. However, the goal of the study was not the final product. The study was focused on the mechanism of the thermal decomposition of bulk and supported nitrates as well as the differences in the decomposition path and they possible reasons.
Materials and methods
Sample preparation
The samples of supported nitrates were prepared by impregnation the Al2O3 (<500 nm, analytical grade, Aldrich) with an aqueous solution of respective nitrate using the necessary amount of solution for the filling of the support pores. The concentration of the solutions of metal nitrate hydrates: Ni(NO3)2·6H2O, Co(NO3)2·6H2O, Zn(NO3)2·6H2O, Cu(NO3)2·3H2O, and Mn(NO3)2·6H2O (analytical grade, Aldrich) used was 3 mol dm−3. 200 mg of Al2O3 was dispersed in 0.5 mL of each metal nitrate solution and mixture has been blended for several minutes. Next impregnated alumina supports were dried for twenty-four hours at 30 °C on air.
The samples of bulk nitrates were prepared by drying respective nitrate hydrate for twenty-four hours at 30 °C on air. After drying the hydration water content in compounds studied could not be exactly determined, specially for supported samples, that is why we denote water content as xH2O per mole of nitrate.
Methods
Thermal decomposition was performed on an apparatus that enabled simultaneous recording of TG and DTA signals (SDT 2960, TA INSTRUMENTS). This apparatus was connected on-line with a quadrupole mass spectrometer (QMD 300 THERMOSTAR, BALZERS) so that parallel analysis of gaseous products of the reaction was carried out. The energy of the ion source was 70 eV and a Faraday detector was used.
Ion currents for M/q values equal to 18, 30, 44, and 46 were monitored (where M is molecular mass of particle, and q the particle charge). Selected M/q values correspond to the following molecular and fragmentation ions which can be formed during decomposition of nitrates: H2O+, NO+, N2O+, NO +2 . All intensities of ion peaks were first corrected for the background. Measurements were performed in the synthetic air atmosphere (99,999 %, H2O content less than 3 ppm) with flow rate of 9 dm3 h−1. The samples of mass about 15 mg of bulk Me(NO3)2·xH2O and 30 mg of supported Me(NO3)2·xH2O/Al2O3 were heated in the platinum crucible with the rate 1 deg min−1. The gas sampling capillary was placed directly above the vessel. All the data were gathered by an on-line computer system with the commercial software (TA INSTRUMENTS, BALZERS).
The analysis of recorded mass spectrum of gaseous products of decomposition was performed consider the possible products of decomposition along with the fragmentation processes—mainly the origin of M/q = 30 line not only from the NO but also from the fragmentation of NO2 and N2O. Thus, the M/q = 18 and M/q = 46 ion current lines describe liberation of H2O and NO2, respectively. However, small amounts of NO (M/q = 30) and tracers of N2O (M/q = 44) were also observed in the gaseous products of decomposition. Moreover, the shape of M/q = 30, 44, and 46 ion current lines suggest that NO, N2O, and NO2 are liberated during the same stages of decomposition therefore they all are the results of nitrate groups decomposition. To minimize the numbers of ion current lines presented in the figures, the M/q = 46 line was chosen to present not only the emission of NO2 but also the products of nitrate groups decomposition in general.
The composition of initial sample, intermediates, and residue was analysed by X’Pert Pro X-ray diffractometer (PHILIPS Panalytical) using CuKα radiation.
The morphological characteristics of samples was investigated using JEOL JSM 5400 scanning electron microscope.
Results
Co(NO3)2·xH2O
Thermal decomposition of bulk cobalt nitrate hydrate proceeds in several not well-separated stages (Fig. 1). The dehydration starts at room temperature (25 °C) and occurs in five steps that is clearly seen on DTA curve (Fig. 1b) and on mass spectral signals (Fig. 1c). Dehydration associated with several DTA peaks indicates the complexity of dehydration process and proves the formation of series of lower hydrates. The composition of these lower hydrates cannot be calculated based on mass loss because none of them forms the stable phase at the conditions of experiment. At about 175 °C dehydration finishes (MS signal for H2O in Fig. 1c disappears) and decomposition of nitrates begins (MS signal for NO2 appears). However, small amount of nitrogen oxides are evolved below 175 °C what suggests that during dehydration decomposition of nitrate groups proceeds probably on the material surface, which is highly probable for nitrates. At about 250 °C bulk cobalt nitrate is fully decomposed. The steps on TG curve as well as endothermic effects on DTA curve in the temperature range of 20–250 °C are connected with corresponding effects on mass spectra.
In the case of cobalt nitrate supported on Al2O3 dehydration proceeds in three stages. It starts at about 40 °C and is completed at 140 °C, that is temperature 35 °C lower than the end of dehydration of bulk cobalt nitrate. The nitrogen oxides start to release just after dehydration completes at 140 °C which is temperature about thirty-five degrees lower than that for the bulk cobalt nitrate. Though traces of nitrogen oxides are evolved during the dehydration, similar as it was observed for bulk cobalt nitrate. The decomposition of supported cobalt nitrate is finished at about 210 °C. The SEM microphotograph of the residue is shown in Fig. 2a.
The final product of bulk cobalt nitrate decomposition is Co3O4, which was confirmed by XRD analysis (not shown here) and stays in agreement with results presented in the literature [22, 24]. Decomposition of cobalt nitrate supported on Al2O3 leads to CoAl2O4 spinel as the final product at the temperature 210 °C (Fig. 2b). As it is in detail described in the literature, the decomposition of cobalt nitrate on alumina leads to oxide mixture (Al2O3 and Co3O4) or CoAl2O4 spinel, depending on the support synthesis method [25]. However, highly dispersed support can imply the spinel formation even in the relatively low temperature.
Ni(NO3)2·xH2O
The decomposition of nickel nitrate hydrate (Fig. 3) proceeds in several stages like in the case of cobalt nitrate. The dehydration of bulk nickel nitrate hydrate as well as supported one begins at room temperature, but the course of dehydration in both cases is different. Dehydration of bulk nickel nitrate goes through several not well-separated stages and finishes at about 210 °C. For the supported nickel nitrate four well-separated stages of dehydration are observed and the release of hydration water is completed at 175 °C, which is reflected on MS signal of H2O (Fig. 3c).
The decomposition of anhydrous nitrate obtained from bulk nickel nitrate hydrate is one-stage process occurring between 225 and 310 °C. The MS signals for H2O and NO2 obtained during decomposition of supported nickel nitrate reveal evolution of traces of nitrogen oxides at about 125 °C that is before completion of dehydration. The main decomposition of nitrate groups of supported nickel nitrate begins at 190 °C and is two-stage process, which is confirmed by DTA peaks and MS signals (Fig. 3d). At 280 °C, the MS signal for nitrogen oxide disappears that indicates the completion of nitrate groups decomposition; however, on the TG curve (Fig. 3a) the slight decrease of sample mass to 375 °C can be seen, resulting probably from the slow desorption of gaseous product from the support surface.
The final product of nickel nitrate hydrate decomposition of both samples is nickel oxide NiO. Figure 4 shows SEM microphotograph and the results of XRD analysis of the decomposition residue of nickel nitrate supported on Al2O3.
Mn(NO3)2·xH2O
Decomposition of bulk manganese nitrate hydrate is a multistage process with overlapping steps (Fig. 5). As can be seen on DTA curve (Fig. 5b) bulk compound melts at about 35 °C and next undergoes dehydration. Before completing dehydration around 135 °C degradation of nitrate groups begins. This statement is based on MS spectra (Fig. 5c–d)—it is seen that between 135 and 175 °C the rest of H2O evolves together with NO2. The conclusion is that anhydrous manganese nitrate is not formed during decomposition. The residue of decomposition at 300 °C is MnO2.
As can be seen on DTA/TG curves (Fig. 5), decomposition of nitrate supported on Al2O3 starts at about 110 °C which is the temperature lower than that for bulk substance. Decomposing occurs through overlapping stages not separated on TG curves, which are preceded by melting of sample. Mass spectrum analysis showed that below 110 °C water is the only volatile product of decomposition. Above 110 °C, several steps of decomposition occur which is specially clearly seen on DTA curve (Fig. 5b). Between 110 and 210 °C, evolution of NO2 together with H2O is observed similarly as for bulk manganese nitrate hydrate; however, the range of temperature is broadened. The final product of thermal decomposition of manganese nitrate is MnO2. However, as it is seen on Fig. 5a manganese(IV) oxide can be decomposed to Mn2O3 at 600 °C. Furthermore, the results of XRD analysis (Fig. 6b) of solid residue of decomposition of manganese(II) nitrate supported on Al2O3 taken from the temperature 600 °C confirm decomposition to mixture of manganese(III) and aluminium oxides. SEM microphotograph and XRD results (Fig. 6) suggest that both Al2O3 and Mn2O3 exhibit a low degree of crystallinity.
Zn(NO3)2·xH2O
Bulk zinc nitrate hydrate (Fig. 7) starts to dehydrate at about 30 °C. Dehydration is accompanied by melting of a compound at 35 °C (sharp, endothermic DTA peak on Fig. 7). According to MS analysis, signal from water disappears at 120 °C which means that dehydration finishes at this temperature. Decomposition of nitrate groups starts at 75 °C and is finished at 265 °C when ZnO as final product is formed. However, when we analyse the shape of TG curve, the stage of dehydration is not separated from the stage of nitrate groups decomposition. Decomposition of zinc nitrate hydrate supported on Al2O3 proceeds at the beginning similarly to the decomposition of bulk material. Dehydration and melting of hydrate in a comparable temperature (around 40 °C) can be noticed. The differences show when decomposition of nitrate groups starts. NO2 was detected in gaseous products starting from 60 °C together with H2O. The second stage of nitrogen oxides evolution appeared at 175 °C. The decomposition of supported Zn(NO3)2 finished about 320 °C.
The final product of decomposition, ZnO, forms on the surface of Al2O3 flower-shaped grains which actually consist of wurtzite-type crystals (Fig. 8).
Cu(NO3)2·xH2O
Cu(NO3)2 hydrate decomposes by overlapping stages. As can be seen in (Fig. 9) bulk Cu(NO3)2 hydrate starts to lose mass at about 75 °C in several not separated stages. Almost at the temperature of the beginning of dehydration, nitrogen oxides starts to evolve (Fig. 9d). The dehydration and decomposition of nitrate groups proceed simultaneously to 225 °C when dehydration finishes. Releasing the water vapour at temperatures about 200 °C suggests evolving constitution water rather that hydration one. Especially as Cu(NO3)2·3Cu(OH)2 or Cu2(OH)3(NO3) according to the literature can be identified as solid intermediate during copper nitrate decomposition [26, 27]. Complete decomposition of bulk cooper nitrate hydrate finishes at 250 °C. It should be noticed that the last stage of decomposition (225–250 °C) is combined only with degradation of nitrates groups.
It should be noticed that the mechanism of decomposition of copper nitrate supported on Al2O3 is significantly different as the decomposition of bulk material. In case of supported Cu(NO3)2 hydrate two stages of dehydration can be observed. Dehydration starts at 60 °C and is associated with one endothermic peak on DTA (Fig. 9b) and adequate signal on MS spectrum (Fig. 9c). The second stage of dehydration occurs between 175 and 225 °C. Decomposition of nitrate groups proceeds at the same temperature ranges as dehydration does. Thus, elimination of water from the structure is always accompanied with degradation of nitrate groups even in the relatively low temperature (about 70 °C). At the temperature of 225 °C copper nitrate supported on Al2O3 is fully decomposed.
The final product of Cu(NO3)2 hydrate decomposition in both cases is monoclinic CuO (Fig. 10b). CuO crystals which were formed on the Al2O3 support have a needle-shaped form (Fig. 10a).
Discussion and conclusions
Analysis of the temperatures of the beginning of dehydration (T deh) and temperatures of the end of decomposition (T fin) of adequate bulk and supported nitrates (Table 1) leads to conclusion that there are no significant differences and correlations between those temperatures.
In case of temperatures of the beginning of decomposition (T decomp), the differences are not significant as well but we observe the general dependence that temperature of decomposition of supported nitrate is lower than temperature of decomposition of adequate bulk nitrate (Fig. 11). The lowest temperature of decomposition occurs for Cu(NO3)2, and the highest for Ni(NO3)2.
No significant correlation between the atomic properties of d-metals, listed in Table 2, and temperature of decomposition were found, may be with one exception concerning some slight correlation between covalent radius of cation and the T decomp. The lack of significant correlations seems to indicate that the main role in decomposition of studied nitrates plays processes which occur in the nitrate ion; however, the modifications in the electron and geometric structure of NO3 − ion resulted from its different surroundings can be responsible for changes in the picture of decomposition of individual nitrates.
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This work has been performed with the financial support of the Polish Ministry of Science and Higher Education, under the Grant No. 11.11.160.438.
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Barbara Małecka—Deceased.
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Małecka, B., Łącz, A., Drożdż, E. et al. Thermal decomposition of d-metal nitrates supported on alumina. J Therm Anal Calorim 119, 1053–1061 (2015). https://doi.org/10.1007/s10973-014-4262-9
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DOI: https://doi.org/10.1007/s10973-014-4262-9