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Article

Mechanochemical Synthesis of CuO/MgAl2O4 and MgFe2O4 Spinels for Vanillin Production from Isoeugenol and Vanillyl Alcohol

by
Behgam Rahmanivahid
1,2,
Maria Pinilla-de Dios
2,
Mohammad Haghighi
3 and
Rafael Luque
2,4,*
1
Esfarayen University of Technology, Esfarayen 96619-98195, Iran
2
Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Córdoba, Campus de Rabanales, Edificio Marie Curie (C-3), Ctra Nnal IV-A, Km 396, E14014 Córdoba, Spain
3
Chemical Engineering Faculty, Sahand University of Technology, P.O. Box 51335-1996, Sahand New Town, Tabriz 53318-11111, Iran
4
Peoples Friendship University of Russia (RUDN University), 6 Miklukho Maklaya str., 117198 Moscow, Russia
*
Author to whom correspondence should be addressed.
Molecules 2019, 24(14), 2597; https://doi.org/10.3390/molecules24142597
Submission received: 4 June 2019 / Revised: 8 July 2019 / Accepted: 15 July 2019 / Published: 17 July 2019
(This article belongs to the Special Issue Recent Development of Mechanochemical Synthesis)
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Abstract

:
CuO/MgAl2O4 and CuO/MgFe2O4 catalysts were successfully synthesized with the use of spinel supports by a very simple and low-cost mechanochemical method. High-speed ball-milling was used to synthesize these catalyst supports for the first time. Materials were subsequently characterized by using XRD, FESEM, TEM, EDS-Dot mapping, XPS, BET-BJH, and Magnetic Susceptibility to investigate the physical-chemical characteristics of the catalysts. Acidity evaluation results indicated that the catalyst with the Mg-Al spinel support had more acid sites. XRD results showed a successful synthesis of the catalysts with large crystal sizes. Both catalysts were used in isoeugenol oxidation and vanillyl alcohol to vanillin reactions, with the CuO/MgAl2O4 showing optimum results. This catalyst provided 67% conversion (74% selectivity) after 2 h and this value improved to 81% (selectivity 100%) with the second reaction after 8 h. The CuO/MgFe2O4 catalyst in the first reaction after five hours revealed 53% conversion (47% selectivity) and after eight hours with the second reaction, the conversion value improved to 64% (100% selectivity). In terms of reusability, CuO/MgAl2O4 showed better results than the CuO/MgFe2O4 catalyst, for both reactions.

1. Introduction

Vanillin is a chemical compound from the aromatic aldehydes family with many industrial applications [1]. This valuable substance is used in perfumes, food, cosmetics, pharmaceuticals, and other chemical industries [2,3,4]. Vanillin naturally exists in some plant families which have been used for extracting it in so many different ways [5]. According to the multiple uses of vanillin, the annual required amount of this material has been estimated at 12,000 tons. Nowadays, due to the lack of natural resources (less than 1% is provided from them) and considering the low price of synthetic vanillin, this substance is produced by industrial methods [6,7]. There are various industrial methods to produce vanillin. One of them is the bioconversion of materials such as vanillyl alcohol, vanillic acid, creosol, phenolic stilbenes, glucose, lignin, isoeugenol, and eugenol [8,9,10]. Another method to produce vanillin is using biocatalysts because the marginal cost of the product then becomes very low [11,12,13,14]. Chemical synthesis of vanillin from lignin, guaiacol, coniferin, ferulic acid as raw materials is also an important way to produce this substance [3,15,16]. In recent years, vanillin production by the oxidation of some materials such as isoeugenol and vanillyl alcohol has been considered [7,17,18]. In this method, raw materials with an oxidizer such as hydrogen peroxide in the presence of a catalyst with the ability of oxidation produce vanillin [19]. There are several catalysts with oxidation ability which are used in various industries. Some of these catalysts such as Cu-Ti composite, Mn-doped ceria, and Co3O4 were used in the vanillin production reaction [17,18,19]. However, these catalysts need high temperature and pressure or a significant time for this reaction. Also other catalysts such as Pd [20,21], Mn2O3 [22,23,24], and Au [25,26,27] have been used in oxidation reactions of CH4, CO, NO, and CH4O. In several references, CuO was used as a powerful catalyst for oxidation reactions [28,29,30,31]. It seems that these metal oxides, due to their low cost and high oxidation power, are suitable catalysts for the oxidation of isoeugenol and vanillyl alcohol. In this work, CuO was employed as active phase for the synthesis of CuO-based catalysts in view of their application in the selective oxidation of isoeugenol to vanillin. Mg-Al and Mg-Fe spinels (MgAl2O4 and MgFe2O4) were selected as supports due to their previously reported convenient catalytic properties [32,33,34,35].
In recent years, mechanochemistry emerged as a relevant methodology for the synthesis, preparation, and design of nanomaterials [36]. MgFe2O4 and MgAl2O4 spinels were previously synthesized via a mechanochemical method by other researchers, but, with low speed, lengthy, and energy intensive ball-milling conditions (e.g., over 12 h) [37,38]. In this work, high speed ball-milling mechanochemistry was employed as a simple and low-cost methodology, for the first time, in the synthesis of these spinels.
Various analyses, such as X-ray Powder Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Transmission Electron Microscopy (TEM), BET Surface Area and BJH Pore Size, Energy Dispersive X-Ray Spectroscopy (EDS)-Dot mapping, X-Ray Photoelectron Spectroscopy (XPS), and Magnetic Susceptibility, were used to determine the characteristics of the synthesized catalysts.

2. Results and Discussion

2.1. Characterization of the Nanocatalysts

2.1.1. XRD Analysis

XRD analyses of the synthesized samples are shown in Figure 1. Comparing the analysis of the CuO/MgAl2O4 sample with the standard peaks of MgAl2O4 spinels (JCPDS: 01-086-0083; Cubic, 2θ = 19.0, 31.3, 36.8, 44.8, 55.6, 59.3, 65.2, and 77.3), the successful synthesis of this spinel as catalyst support could be easily recognized. However, comparing the analysis of this sample with the standard patterns of CuO (JCPDS: 01-080-1268; 2θ = 35.5, 35.7, 38.8, 39.0, 48.7, 53.5, 58.4, 61.6, 65.9, 66.3, and 68.2), no significant peak was observed in these samples.
This phenomenon represents an appropriate and uniform distribution also with small particles of CuO on the surface of the catalyst support [32]. This occurs due to the use of the mechanochemical method in the distribution of the active phase on the catalyst support. Furthermore, peaks of CuO/MgFe2O4 corresponding to the standard patterns of MgFe2O4 (JCPDS: 01-073-2211; Cubic, 2θ = 30.2, 35.6, 43.2, 53.6, 57.2, 62.8, and 74.3) were observed, which confirms the successful synthesis of this spinel. Also, studying the analysis of this sample and standard peaks of CuO, no peak was observed. This phenomenon can be attributed to the low ratio of the active phase to the support (0.5 wt%), to the proper and uniform dispersion, and also to the small particle size due to the use of a mechanochemical method. Crystal sizes of these two samples are shown in Table 1, which are calculated by the Scherrer equation [39]. These results showed sizes of 25.9 nm and 78 nm for the CuO/MgAl2O4 and CuO/MgFe2O4 samples, respectively. Larger crystal sizes of the synthesized sample with magnetic support indicate that this sample has a lower surface size than the other sample.

2.1.2. TEM and SEM Analysis

TEM analyses of the synthesized samples are shown in Figure 2. TEM images of CuO/MgAl2O4 (Figure 2a) indicate that the average particle size of this catalyst is smaller than 100 nm and, with more detail, crystalline forms of the particles can be seen. On the contrary, the analysis of CuO/MgFe2O4 (Figure 2b) shows that the particle size is around 200 nm and also the formation of large crystals can be seen in this sample. The minimum, maximum, and average particle size of both samples are shown in a particle size distribution plot. The average particle sizes obtained of CuO/MgAl2O4 and CuO/MgFe2O4 were 39 nm and 121 nm, respectively, which is in good agreement with results of crystal size.
Due to the magnetic properties of MgFe2O4, the associated TEM images are not more transparent than the other sample. SEM analysis of CuO/MgAl2O4 and CuO/MgFe2O4 catalysts which are shown in Figure 3 confirm the results of TEM analysis. These analyses show that the particles of CuO/MgAl2O4 (Figure 3a) are smaller than the particles of CuO/MgFe2O4 (Figure 3b). Particle sizes with a magnetic support are large so the crystal regular form can be easily observed.
Both catalysts were found to be non-porous materials. However, due to the small particle size of the CuO/MgAl2O4 catalyst, it can be predicted that its surface area is higher than the other catalyst area. It is noteworthy that the results of this analysis confirmed the XRD analysis results.

2.1.3. EDX Analysis

EDX analysis was carried out to determine the distribution of the elements on each catalyst surface and its impact on the activity of the catalysts in the reaction [40,41]. EDX-dot mapping analysis was used for both CuO/MgAl2O4 and CuO/MgFe2O4 catalysts, respectively. Results are shown in Figure 4. Mg, Al, and O elements follow a uniform distribution in the CuO/MgAl2O4 sample which results in a proper and uniform formation of this spinel. Dot mapping of Cu element in this catalyst shows a highly proper and uniform distribution of CuO on the support surface, as the active phase. On the other hand, CuO/MgFe2O4 catalyst follows a uniform distribution of Mg, Fe, and O elements and shows also a good distribution of Cu on the support surface. Both element weight distributions are consistent with the theoretical data. It can be said that these uniform distributions are attributable to the mechanochemical synthesis method. This method forces a proper mix of the components of the spinel support synthesis and also an appropriate distribution of the active phase (CuO) on the supports (MgAl2O4 and MgFe2O4) [42,43].

2.1.4. XPS Analysis

The surfaces of both synthesized samples were studied by XPS analysis and the results are shown in Figure 5 and Figure 6. Before analysis, the peak locations for both samples were calibrated according to the peak of C1s (adsorbed species CO and CO2) which appears at 284.6 eV. Figure 5 shows peaks at 724.6 and 711.1 eV which are related to Fe2p3/2 and Fe2p1/2 respectively. They confirmed the existence of Fe3+ species in the CuO/MgFe2O4 catalyst.
The presence of the Mg2p peak at 48.9 eV is related to Mg2+ in the sample. So, it is possible to conclude the successful formation of MgFe2O4 spinel [44,45,46]. The O1s peak at 529.8 eV belongs to the Mg–O, Fe–O bond or is related to absorbed oxygen of various species on the catalyst surface [44,45,46]. In this case, the peak of CuO was not observed correctly which may be due to the very low amount (0.5 wt%) and also XPS is a local/superficial analysis [47].
The XPS image corresponding to the CuO/MgAl2O4 catalyst is shown in Figure 6. Peaks at 50.3 eV and 74.7 eV which are related to Mg2p and Al2p, indicate the presence of Mg2+ and Al3+ species in this sample which proves the successful synthesis of MgAl2O4 spinel [47,48,49]. Also various species of O1s detected in the synthesized samples at 531.5 and 532.5 eV peaks are related to Al–O and Mg–O bonds, respectively and also the peak at 530.2 eV, because of the oxygen of absorbed species on the catalyst surface or it is related to Cu–O bond in the active phase [49,50]. For Cu2+ species, the peaks at 934.0 and 954.0 eV are related to Cu2p in this sample which shows the existence of CuO on the catalyst surface [51]. It should be noted that a partial change in peak locations of some species, with decreasing or increasing bonding energy, is due to a change in the energy level of various species in different environments [45,52,53,54]. Results from this analysis support the results from XRD and EDS analysis.

2.1.5. BET-BJH Analysis

The surface area and pore diameter of the catalyst are two key characteristics to be evaluated in all catalysts. Synthesized catalysts were evaluated by BET-BJH analysis and the results are shown in Table 1 and Figure 7. According to the table, the surface areas of CuO/MgAl2O4 and CuO/MgFe2O4 catalysts were 20 m2/g and 3 m2/g, respectively. The reason for the very small surface area of the CuO/MgFe2O4 catalyst is its large particle and crystal size which is demonstrated in XRD and FESEM analysis.
From Figure 7, which shows the adsorption and desorption isotherms of the synthesized samples, these catalysts can be easily categorized into type III of the IUPAC classification. The hysteresis forms of the samples indicate that both synthesized catalysts are non-porous and have plate structures, so the samples have an inter-particle surface. However, according to Table 1, the obtained pore diameters for CuO/MgAl2O4 and CuO/MgFe2O4 catalysts are 51.4 nm and 18.2 nm, respectively. These results confirm previous analyses, such as XRD and SEM.

2.1.6. Acidity

Pyridine (PY) and 2,6-dimethylpyridine (DMPY) absorption methods were used at 200 °C (pulse chromatographic titration methodology) to investigate the acidity of CuO/MgAl2O4 and CuO/MgFe2O4 catalysts [55,56,57]. Through the PY absorption, it is possible to obtain the total amount of acid sites. By the DMPY absorption method, Brönsted acid sites can be determined. Lewis acid sites are calculated by subtracting these values from each other [58]. The results of this method can be seen in Table 2. According to the results, the total amount of acid sites of the CuO/MgAl2O4 catalyst (69 μmol PY/g) is higher than the amount of the CuO/MgFe2O4 catalyst (38 μmol PY/g). However, the amount of Lewis acid sites is almost the same for both samples (26 μmol PY/g). The reason for the difference in the value of Brönsted acid sites and the coincidence on the value of Lewis acid sites is the magnetic support of MgFe2O4 which is related with the surface area. The effect of acid sites was further determined by examining the catalyst activity.

2.1.7. Magnetic Susceptibility Analysis

Magnetic properties of CuO/MgAl2O4 and CuO/MgFe2O4 catalysts are shown in Table 2. Due to the use of Mg-Fe spinel in the synthesis of CuO/MgFe2O4 as catalyst support, this sample showed a highly desirable magnetic susceptibility of 416 × 10−6 m3/kg. On the contrary, the synthesized catalyst with Mg-Al spinel does not have magnetic susceptibility. According to the magnetic behavior of the CuO/MgFe2O4 catalyst, this sample has a great ability to be separated easily from the reaction mixture which can be considered an advantage for this catalyst.

2.2. Catalytic Performance Study toward Vanillin Production

In order to evaluate the synthesized catalysts activity, CuO-based spinel systems were employed in oxidation reactions of isoeugenol and vanillyl alcohol to vanillin. To carry out these reactions, an oxidizer (hydrogen peroxide) and a solvent (acetonitrile) were used. Both reactions were carried out at a temperature of 90 °C. After using GC to obtain the amount of the reaction products, the conversion and selectivity of each reaction were calculated. Results are shown in Figure 8 and Figure 9. To determine the behavior of each catalyst in the reaction, first both vanillin production reactions were performed at 90 °C (isoeugenol oxidation) and 40 °C (vanillyl alcohol oxidation) over 24 h without any catalyst (Table 3 and Table 4, respectively). Using the synthesized catalysts, the results showed that CuO/MgAl2O4 catalyst has a very good activity in the isoeugenol oxidation reaction. After two hours of reaction, conversion reached 67%. The selectivity of vanillin production was 74%, at the same time. After 8 h with the same catalyst, conversion was 81% and the selectivity in the oxidation reaction of vanillyl alcohol to vanillin was raised to 100%. The performance of CuO/MgFe2O4 was not so efficient. With this catalyst, after 2 h, the conversion was 36% with a selectivity of 39% in the vanillin production reaction from isoeugenol. After 5 h, the conversion increased to 53% with a selectivity of 46%. After 8 h of the oxidation reaction of vanillyl alcohol, the conversion was 64% with a selectivity of 100%.
Taking into account the results, it is possible to determine that the Mg-Al spinel support exhibited a comparably superior performance to that of Mg-Fe spinel. This may be due to the greater surface area and pore volume of CuO/MgAl2O4. Active sites for this reaction were previously reported to be moderate acidic and/or redox metal sites, in this case being a synergistic combination between the CuO phase and the spinel support. Another important characteristic of heterogeneous catalysts is their reusability. The CuO/MgAl2O4 catalyst was used four consecutive times in the isoeugenol and vanillyl alcohol oxidation reaction over 2 and 8 h, respectively and CuO/MgFe2O4 catalyst was used over 5 and 8 h. For this purpose, CuO/MgAl2O4 and CuO/MgFe2O4 catalysts were separated once finished from the reaction mixture with filter paper and by a magnet, respectively. Then, they were oven-dried for 24 h at 110 °C to use again in reactions. From Figure 9, the first reuse of CuO/MgAl2O4 catalyst in the vanillin production reaction from isoeugenol, showed a good performance with a 7% decrease in the conversion and a 13% reduction in selectivity. After the second and third reuse, the conversion changed to 40% and 29%, respectively and the selectivity varied to 42% for the second reuse and 28% for the third one. With the same catalyst, in the oxidation reaction of vanillyl alcohol the conversion gradually decreased to 79% after the first reuse.
For the next iterations, conversion decreased to 56% and 29%, respectively with 100% selectivity. On the other hand, the CuO/MgFe2O4 catalyst showed different results. In both reactions, drastic reductions were observed after their reuse. The conversion of this catalyst in the isoeugenol oxidation reaction after the first reuse was 29% with a selectivity of 23%. After the second and third iterations the conversion was almost constant at 17% with a selectivity of 8%. The conversion of this catalyst after the first reuse in the vanillyl alcohol oxidation reaction was 42%. This value decreased to 26% and 25% after the second and third reuse, respectively. According to the results, it is possible to conclude that both catalysts CuO/MgAl2O4 and CuO/MgFe2O4 have good ability to produce vanillin from vanillyl alcohol and isoeugenol. Based on the analysis and the values from conversion, selectivity and reusability, it can be said that the MgAl2O4 spinel is the most appropriate support for the active phase of CuO to perform both reactions.

3. Conclusions

CuO/MgAl2O4 and CuO/MgFe2O4 catalysts with spinel supports were synthesized for the first time by using a mechanochemical method (high-speed ball-milling) as a quick and efficient method. The active phase of CuO was distributed on the catalyst surface using conventional (low speed) ball milling. With this method, the synthesis time and the costs were significantly reduced. Results from different analyses showed that CuO/MgFe2O4 catalyst had higher particle and crystal size than CuO/MgAl2O4 catalyst which is related to the small surface area. Larger particle size caused a smaller area. Both catalysts used in the oxidation reaction of isoeugenol and vanillyl alcohol showed a good ability to produce vanillin. CuO/MgFe2O4 catalyst showed high magnetic susceptibility and therefore easy separation from the reaction mixture. In both reactions comparing the conversion, selectivity, and reusability of the catalysts, CuO/MgAl2O4 presented better characteristics for these reactions, explainable because of its surface area and acid sites.

4. Materials and Methods

4.1. Materials

Magnesium oxide (MgO 99%, Aldrich, St. Louis, MO, USA), aluminum oxide (Al2O3 99%, Panreac, Barcelona, Spain), iron oxide III (α-Fe2O3 99%, Merck, Kenilworth, NJ, USA) and hydrated copper chloride (CuCl2.2H2O 99.8%, Sigma-Aldrich, St. Louis, MO, USA) were used to synthesize CuO/MgAl2O4 and CuO/MgFe2O4. Isoeugenol (C10H12O2 98%, Aldrich), acetonitrile (C2H3N 99.8%, Panreac), vanillyl alcohol (C8H10O3 98%, Aldrich), and hydrogen peroxide (H2O2 50 wt% in H2O, Sigma-Aldrich) were used for vanillin production reactions. All reagents were used without further purification.

4.2. Preparation and Procedure of the Nanocatalysts

The synthesis procedure of CuO/MgAl2O4 and CuO/MgFe2O4 nanocatalysts is shown in Figure 10. As can be seen, for the synthesis of MgAl2O4 spinel, stoichiometric amounts of MgO and Al2O3 were mixed by high speed ball milling (Emax model, Retsch, Haan, Germany) at 900 rpm for 1 h. Then, the obtained mixture of oxides was calcined in a furnace with air flow at 900 °C for 3 h. After preparing the spinel support for the deposition of CuO active phase on its surface, specific amounts of hydrated copper chloride and MgAl2O4 (to achieve a 0.5 wt% CuO in the final material) were mixed by conventional ball milling (PM 100 model, Retsch, Germany) at 350 rpm for 10 min. Finally, to synthesize the CuO/MgAl2O4 catalyst, ball milled samples were calcined at 400 °C for 2 h (Figure 10).
To synthesize the CuO/MgFe2O4 catalyst, the whole synthesis process was performed as the previous catalyst, but in the synthesis of the magnetic spinel support MgFe2O4, the MgO, and α-Fe2O3 were mixed by high speed ball milling. For other parameters such as stoichiometric ratio, calcination time and temperature, the ball milling speed and time were quite similar to the synthesis process of CuO/MgAl2O4 catalyst.

4.3. Characterization Techniques of the Nanocatalysts

Analysis by X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Transmission Electron Microscopy (TEM), Energy-dispersive X-ray spectroscopy (EDS) Dot mapping, X-ray Photoelectron Spectroscopy (XPS), Brunauer-Emmett-Teller (BET)/Barrett-Joyner-Halenda (BJH) and Magnetic Susceptibility techniques were used to evaluate the characteristics of the synthesized nanocatalysts. Catalyst acidity was determined by the titration method of pyridine and dimethyl pyridine through a gas chromatograph with flame ionization detector (FID) and a packed column Chromosorb AW-MCS 80/100 of 0.5 m. The surface morphology and particle size of the synthesized catalysts were analyzed by using TEM (Transmission Electron Microscopy, JEM-1400 (JEOL, Peabody, MA, USA) analyser) and SEM (Scanning Electron Microscopy, JSM-7800F Prime (JEOL, Peabody, MA, USA) analyzer). Considering the importance of the element composition on the catalyst surface, an XPS analyzer Ultra High Vacuum (UHV) multipurpose surface analysis (Specst model, Berlin, Germany) operating at pressures <10−10 mbar using a conventional X-ray source—XR spectra were recorded on a Bruker D8 X ray diffractometer (10–80° 2ϴ range) in the Bragg-Brentano geometry and in reflection mode, using a Cu X-ray tube, a rotating platform, a monochromatic primary beam, and a high sensitivity detector—and an EDX analyzer X-MaxN (OXFORD Instruments, Abingdon, UK) were applied to obtain the surface elements composition and the material types. The specific surface area and pore diameter of the catalysts were measured by using the BET-BJH method with ASAP 2000 (Micromeritics Instrument, Norcross, GA, USA) device. A MS2 A Magnetic Susceptibility Meter (Bartington Instruments, Witney, Oxon, UK) device was used to determine the magnetic power of the MgFe2O4 spinel.

4.4. Experimental Set-Up for the Catalytic Performance Test

Synthesized catalysts were used in the vanillin production reaction from vanillin alcohol and isoeugenol, to gain an appropriate assessment of their catalytic activity.
The reaction was carried out in a carousel with a Pyrex tube. For the oxidation reaction of isoeugenol, 8 mL acetonitrile, 1.2 mL H2O2 (hydrogen peroxide) solution (20 mmol H2O2), and 0.8 mL isoeugenol (5 mmol) were poured into a Pyrex tube with 0.1 g of catalyst. Products were analyzed at different time intervals by a Gas chromatograph (7890A model, Agilent Technologies, Santa Clara, CA, USA) fitted with a capillary column Petrocol 100 m × 0.25 mm and 0.5 μm and a flame ionization detector (FID). The results were finally confirmed by GC-MS.
Also, for the vanillin alcohol oxidation reaction, 8 mL of acetonitrile was poured into a carousel tube and the temperature was increased to 40 °C to provide suitable conditions for complete dissolution of vanillyl alcohol. Then 0.77 g (5 mmol) of vanillyl alcohol was added to the solvent and after complete dissolution of vanillyl alcohol in acetonitrile, 1.2 mL of hydrogen peroxide with 0.1 g catalyst were added to the reaction mixture. The carousel was adjusted to 90 °C with a magnetic stirrer speed of 800 rpm. To evaluate the progress of the reactions, the reaction mixture was sampled at different times. Sampling was done by a syringe with a filter. To study the reusability of the samples, catalysts were separated after reaction by a paper filter and washed by acetonitrile. Then, they were oven dried at 110 °C for 24 h and re-used in the vanillin production reaction. To obtain conversion and selectivity of the reaction, products were analyzed by the same gas chromatograph and also, results were confirmed by GC-MS.

Author Contributions

Conceptualization, B.R., M.H. and R.L.; methodology, B.R.; validation, M.H. and R.L., investigation, B.R..; resources, R.L.; data curation, B.R. and M.P.d.D.; writing—original draft preparation, B.R. and M.P.d.D.; writing—review and editing, M.H. and R.L.; supervision, M.H. and R.L.

Funding

The publication was prepared with support from RUDN University Program 5-100.

Acknowledgments

The authors gratefully acknowledge Ministry of Science Research and Technology of Iran for the financial support of the research as well as Iran Nanotechnology Initiative Council and Iran Science Elites Federation for complementary financial supports.

Conflicts of Interest

The authors declare no conflict of interest.

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Sample Availability: Samples of the compounds CuO/MgAl2O4 and CuO/MgFe2O4 are available from the authors.
Molecules 24 02597 g001 550
Figure 1. XRD patterns of prepared nanocatalysts: (a) CuO/MgAl2O4, (b) CuO/MgFe2O4.
Figure 1. XRD patterns of prepared nanocatalysts: (a) CuO/MgAl2O4, (b) CuO/MgFe2O4.
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Molecules 24 02597 g002 550
Figure 2. TEM images and size distribution of (a) CuO/MgAl2O4 catalyst, (b) CuO/MgFe2O4 catalyst.
Figure 2. TEM images and size distribution of (a) CuO/MgAl2O4 catalyst, (b) CuO/MgFe2O4 catalyst.
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Molecules 24 02597 g003 550
Figure 3. SEM images of synthesized nanocatalysts: (a) CuO/MgAl2O4, (b) CuO/MgFe2O4.
Figure 3. SEM images of synthesized nanocatalysts: (a) CuO/MgAl2O4, (b) CuO/MgFe2O4.
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Molecules 24 02597 g004 550
Figure 4. EDX elemental dot mapping analysis of (a) CuO/MgAl2O4 and (b) CuO/MgFe2O4 nanocatalysts.
Figure 4. EDX elemental dot mapping analysis of (a) CuO/MgAl2O4 and (b) CuO/MgFe2O4 nanocatalysts.
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Molecules 24 02597 g005 550
Figure 5. XPS data of CuO/MgFe2O4 nanocatalyst.
Figure 5. XPS data of CuO/MgFe2O4 nanocatalyst.
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Figure 6. XPS data of CuO/MgAl2O4 nanocatalyst.
Figure 6. XPS data of CuO/MgAl2O4 nanocatalyst.
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Molecules 24 02597 g007 550
Figure 7. Adsorption/desorption isotherms of the nanocatalysts (a) CuO/MgAl2O4 and (b) CuO/MgFe2O4.
Figure 7. Adsorption/desorption isotherms of the nanocatalysts (a) CuO/MgAl2O4 and (b) CuO/MgFe2O4.
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Molecules 24 02597 g008 550
Figure 8. Catalytic activity at 90 °C of CuO/MgAl2O4 catalyst in the oxidation of isoeugenol to vanillin (top image) and CuO/MgAl2O4 catalyst in the oxidation of vanillyl alcohol to vanillin (bottom image).
Figure 8. Catalytic activity at 90 °C of CuO/MgAl2O4 catalyst in the oxidation of isoeugenol to vanillin (top image) and CuO/MgAl2O4 catalyst in the oxidation of vanillyl alcohol to vanillin (bottom image).
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Figure 9. Catalytic activity at 40 °C of CuO/MgFe2O4 catalyst in the oxidation of isoeugenol to vanillin (top image) and CuO/MgFe2O4 catalyst in the oxidation of vanillyl alcohol to vanillin (bottom image).
Figure 9. Catalytic activity at 40 °C of CuO/MgFe2O4 catalyst in the oxidation of isoeugenol to vanillin (top image) and CuO/MgFe2O4 catalyst in the oxidation of vanillyl alcohol to vanillin (bottom image).
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Figure 10. Mechanochemical synthesis of CuO/MgAl2O4 and CuO/MgFe2O4 nanocatalysts.
Figure 10. Mechanochemical synthesis of CuO/MgAl2O4 and CuO/MgFe2O4 nanocatalysts.
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Table
Table 1. Structural properties of CuO/MgAl2O4 and CuO/MgFe2O4 nanocatalysts.
Table 1. Structural properties of CuO/MgAl2O4 and CuO/MgFe2O4 nanocatalysts.
SpinelSurface Area
(m2/g)		Pore Volume
(cm3/g)		Mean Pore Size
(nm)		Crystallite Size
(nm)
CuO/MgAl2O4200.0918.225.9 a
CuO/MgFe2O4<50.0351.478.0 b
a Crystallite size estimated by Scherrer’s equation at 2θ = 36.8°. b Crystallite size estimated by Scherrer’s equation at 2θ = 35.6°.
Table
Table 2. Acidity and magnetic properties of CuO/MgAl2O4 and CuO/MgFe2O4 nanocatalysts.
Table 2. Acidity and magnetic properties of CuO/MgAl2O4 and CuO/MgFe2O4 nanocatalysts.
NanocatalystMagnetic Susceptibility
(10−6 m3/Kg)		Total Acidity
(µmol PY/g)		Brönsted Acidity
(µmol DMPY/g) 1		Lewis Acidity
(µmol PY/g) 2
CuO/MgAl2O4-694326
CuO/MgFe2O4416381226
1 DMPY: 2,6-dimethylpyridine; 2 PY: Pyridine.
Table
Table 3. Catalytic activity of CuO/MgAl2O4 and CuO/MgFe2O4 catalysts in the oxidation of isoeugenol to vanillin.
Table 3. Catalytic activity of CuO/MgAl2O4 and CuO/MgFe2O4 catalysts in the oxidation of isoeugenol to vanillin.
Molecules 24 02597 i001
EntryCatalystTime (h)Conversion (%mol)Selectivity
VanillinOthers
1Blank218793
2CuO/MgAl2O42677426
31 Reuse CuO/MgAl2O42707624
42 Reuse CuO/MgAl2O42636436
53 Reuse CuO/MgAl2O42404258
64 Reuse CuO/MgAl2O42292872
7Blank5201189
8CuO/MgFe2O45534654
91 Reuse CuO/MgFe2O45504555
102 Reuse CuO/MgFe2O45292377
113 Reuse CuO/MgFe2O4517991
124 Reuse CuO/MgFe2O4517892
Reaction Conditions: 8 mL acetonitrile, 5 mmol isoeugenol, 20 mmol H2O2, 100 mg catalyst, 90 °C.
Table
Table 4. Catalytic activity of CuO/MgAl2O4 and CuO/MgFe2O4 catalysts in the oxidation of vanillin alcohol to vanillin.
Table 4. Catalytic activity of CuO/MgAl2O4 and CuO/MgFe2O4 catalysts in the oxidation of vanillin alcohol to vanillin.
Molecules 24 02597 i002
EntryCatalystTime (h)Conversion (%mol)Selectivity
VanillinOthers
1Blank8210100
2CuO/MgAl2O4881100-
31 Reuse CuO/MgAl2O4884100-
42 Reuse CuO/MgAl2O4879100-
53 Reuse CuO/MgAl2O4856100-
64 Reuse CuO/MgAl2O4829100-
7Blank8210100
8CuO/MgFe2O4864100-
91 Reuse CuO/MgFe2O4865100-
102 Reuse CuO/MgFe2O4842100-
113 Reuse CuO/MgFe2O4826100-
124 Reuse CuO/MgFe2O4825100-
Reaction Conditions: 8 mL acetonitrile, 5 mmol vanillin alcohol, 20 mmol H2O2, 100 mg catalyst, 40 °C

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MDPI and ACS Style

Rahmanivahid, B.; Pinilla-de Dios, M.; Haghighi, M.; Luque, R. Mechanochemical Synthesis of CuO/MgAl2O4 and MgFe2O4 Spinels for Vanillin Production from Isoeugenol and Vanillyl Alcohol. Molecules 2019, 24, 2597. https://doi.org/10.3390/molecules24142597

AMA Style

Rahmanivahid B, Pinilla-de Dios M, Haghighi M, Luque R. Mechanochemical Synthesis of CuO/MgAl2O4 and MgFe2O4 Spinels for Vanillin Production from Isoeugenol and Vanillyl Alcohol. Molecules. 2019; 24(14):2597. https://doi.org/10.3390/molecules24142597

Chicago/Turabian Style

Rahmanivahid, Behgam, Maria Pinilla-de Dios, Mohammad Haghighi, and Rafael Luque. 2019. "Mechanochemical Synthesis of CuO/MgAl2O4 and MgFe2O4 Spinels for Vanillin Production from Isoeugenol and Vanillyl Alcohol" Molecules 24, no. 14: 2597. https://doi.org/10.3390/molecules24142597

APA Style

Rahmanivahid, B., Pinilla-de Dios, M., Haghighi, M., & Luque, R. (2019). Mechanochemical Synthesis of CuO/MgAl2O4 and MgFe2O4 Spinels for Vanillin Production from Isoeugenol and Vanillyl Alcohol. Molecules, 24(14), 2597. https://doi.org/10.3390/molecules24142597

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