; Monika Słota
; Jarosław Polański
Authors place of work:
University of Silesia, Institute of Chemistry, Katowice, Poland
Published in the journal:
Čes. slov. Farm., 2015; 64, 209-211
44<sup>th</sup> Conference drug synthesis and analysis
We tested for the first time the efficiency of SiO2-, Cu-, and Ni-supported Au in deep glycerol oxidation in adiluted and viscous H2O2/H2O liquid phase. Acetic acid (AA), the C2 oxidate, was preferentially formed in such asystem. High conversion (100%) and AA yields (90%) were observed for the sol-gel SiO2-suppported Au in diluted solutions. Although with the increase of glycerol concentration in the viscous liquid phase these values decreased to ca. 40% (conversion) and 20% (AA yield), the addition of acetonitrile improved the AA yield to ca. 40%, while the surfactants were found to be capable of amany-fold enhancement of the catalyst activity at the room temperature highly-viscous liquid phase. High performances were also observed for the bimetallic Au/Cu and Au/Ni catalysts obtained by nano-Au transfer; however, these catalysts were destroyed during the reaction by the Cu or Ni leaching effect.
Nano-Au catalyst (20 mg, 0.1–10.0 μμmol Au) was suspended in amixture of 1.0mL of 30% hydrogen peroxide (10 mmol H2O2) and 0.5mL (0.5–13.6 mol/L) glycerol (Fisher BioReagents® – Glycerol For Molecular Biology) by sonication at room temperature for 10 min (RK 52 H, Bandolin Electronics, 35 kHz). Reagents were stirred at 770 rpm in asealed tube (septa system) placed in athermostated oil bath at 80 °C for 24 h. The resulted reaction mixture was centrifuged and decantated. The supernatant was dissolved into deuterated water and analyzed using 1H and 13C NMR. For quantitative determination of the reaction products we used an external standard procedure with a(NMR Coaxial Small Volume NMR Insert tubes from ARMAR Chemicals) hydroquinone as the reference substance. Additionally, the 2D COSY and HMQC methods were used to identify and quantify products. The spectra were recorded on Bruker Avance 400 or 500 spectrometers with TMS as the internal standard (400 MHz, 1H, 101 MHz 13C or 500 MHz, 1H, 126 MHz 13C) at room temperature. The signal from water was suppressed using 90 water-selective pulses (zggpwg). Optionally this oxidation procedure was modified by the addition of 1.0mL acetonitrile (19.10 mmol) or surfactants: Sulforkanol (sodium laureth sulfate – SLES), Triton X-100, PEG 400, ca. (0.05 wt. %).
The results had an error of ± 2% throughout the experiments. The formation of acetic acid was confirmed using spectroscopic techniques. Eqs.  to  were used to calculate conversion, product selectivity and yield, respectively.
conversion (mol%) = (initial moles of glycerol – final moles of glycerol)/initial moles of glycerol ⋅ 100 
selectivity of products (mol%) = percentage amount of product formed/the total percentage of all product formed ⋅ 100 
yield (%) = conversion of glycerol × selectivity of desired product/100 
Results and discussion
We assumed that treatment of the concentrated glycerol solutions under mild conditions would potentially be amajor advantage for processing waste glycerol. Intuitively, the glycerol concentration that influences the viscosity of asystem should strongly control the glycerol contact with the catalyst surface. In practice, the catalytic reactions of glycerol in water solutions have been performed previously in arelatively diluted solutions, e.g., in the liquid phase: 0.6 mol/L (mol of glycerol per litre of the reaction mixture, if recalculated using data from the literature; glycerol to H2O2 molar ratio amounted to 1 : 4)1) or in the vapor phase: Ar/glycerol/H2O = 5 : 1 : 212) or N2/H2O/Gly = 46/48/63).
In Table 1, we specified the performance of catalytic Au/SiO2 systems in the oxidation of glycerol in the diluted liquid phase; 0.2 mol/L glycerol, whereas glycerol to H2O2 molar ratio amounted to 1 : 37. For the new catalysts, i.e., SiO2-supported Au, both the conversion and selectivity of the process reached as high as 100% and 90 to 99% (Table 1, entries 1 and 3), respectively, while in these conditions, the Au/C system (Table 1, entry 7) provided much lower conversion (ca. 35%). AA (Au/SiO2) or glycolic acid (GA) and aldehyde (Au/C) were the main products observed for the reactions, respectively. The performance of the Au/C system, typically used for catalytic glycerol oxidation4), compares well to the published data for the 1% Au/C (0.6 mol/L glycerol to H2O2 molar ratio 1 : 4), which provides only slightly higher conversions of ca. 40%1).
In non-diluted glycerol solutions, the selectivity to AA can be increased (up to 99.5% selectivity at 40% conversion, 1.0% Au/SiO2) under the addition of acetonitrile (Table 2). It is worth mentioning that the addition of acetonitrile allowed us to decrease the reaction temperature to 60 °C vs. 80 °C in acetonitrile-free conditions; however, anominal glycerol concentration after the addition of acetonitrile was the lower 2.7 mol/L vs. ca. 4.5 mol/L in the acetonitrile-free conditions. Moreover, the addition of acetonitrile (Table 2, entries 2 (+) and 4 (–)) also increases the selectivity of the AA formation for the f-SiO2-supported Au system (AA selectivity ca. 88% and AA yield ca. 21% with acetonitrile, vs. AA selectivity 0.7% and AA yield 0.3% without acetonitrile). Thus, we observed adecrease in conversion but an increase in AA selectivity for the reaction in the acetonitrile/water solution. We proved that no changes occurred for the blind experiment with the catalysts heated in acetonitrile without glycerol (results not shown).
Thus far, the results of the exhaustive oxidation of glycerol indicated that catalyst availability is of major importance for the observed performance of the system. Below, we report the results of the experiments in which we tested possible applications of the surfactants to improve this feature (Table 3). We observed that aconversion and the yield of AA can be almost doubled at room temperature when Sulforoktanol, PEG 400, or Triton X-100 was used as surfactants.
We observed that, within the complex network of possible reactions, aprocess of deep glycerol oxidation proceeded on Au/SiO2 catalysts preferentially to acetic acid. The selectivity of glycerol oxidation to C3 products was investigated thoroughly. It is not acoincidence, because only C3 oxygenates can form the single carbonous products of glycerol processing, while any oxidation to C2 must also yield the C1 oxygenate (C3 → C2 + C1). This means that, although the process can be fully selective, we obtain at least two products.
Thus, the reactivity to C3 products has been well described, in contrast to the C1 and C2 products. Herein, we described the systems providing high selectivity to acetic acid, the C2 glycerol oxygenate. High conversions (100%) and acetic acid yields (90–99%) were observed for the best catalysts in the diluted aqueous glycerol solutions. Although in arelatively viscous liquid phase these values decreased to ca. 40% and 20%, the addition of acetonitrile could improve the acetic acid yield to ca. 40%, while surfactants were found to be capable of amany-fold enhancement of the catalyst activity. However, this was relatively low at the room temperature highly-viscous liquid phase.
In summary, SiO2-supported Au NPs can form an interesting catalytic system for deep selective glycerol oxidation to acetic acid in undiluted viscous liquid solutions. This seems especially interesting for the processing of glycerol wastes.
The research was co-financed by the National Research and Development Center (NCBiR) under Grant ORGANOMET No: PBS2/A5/40/2014. Author Maciej Kapkowski expresses his appreciation for the support of the DoktoRIS – Scholarship program for innovative Silesia, which is co-financed by the European Union within the framework of the ESF.
Conflicts of interest: none.
*This is a short conference communication version of a publication which appeared in a full form in Kapkowski M, et al, J. Catalysis 2014; 319, 110–118.
prof. Jarosław Polański
University of Silesia, Institute of Chemistry
Szkolna 9 Street, 40-007 Katowice, Poland
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