Glycerol carbonate (GC) and glycidol (GD) are commercial products possible from glycerol transformation, which has become a subject of great importance. Among several basic catalysts screened in this work, BaO showed the highest glycerol conversion of 71% with almost complete selectivity to GC. A tandem synthesis of GD with a selectivity as high as 80% with 98% glycerol conversion could be achieved with mixed oxides of Ba and lanthanides (La and Ce) prepared by the coprecipitation method. Although BaO alone showed the highest basicity as measured by CO 2 TPD, tuning of basicity by incorporation of CeO 2 resulted in the formation of GD. Incorporation of Ba into the ceria matrix induced oxygen vacancies in the cerium oxide material. The presence of u″/v″ doublets at 888.7 and 903.2 eV, respectively, in XPS of the Ba−Ce sample also confirmed the oxygen vacancies in the lattice. In this tandem approach to GD, the subsequent decarboxylation of initially formed GC was due to the presence of a CeO 2 lattice with defects, which is known to be the best for CO 2 adsorption. Increase in both catalyst loading and temperature showed a dramatic enhancement in GD selectivity. A plausible reaction pathway for the transesterification of glycerol with DMC to give GC followed by its decarboxylation to GD is also proposed based on the structural characterization and activity studies.

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Glycerol carbonylation with urea is a very feasible option to produce glycerol carbonate with a net result of CO 2 fixation through urea synthesis. The prerequisite of an efficient catalyst for this reaction is to possess both acid and basic sites together. Several acidic supports were screened for ZnO catalyst in this work and Zn/MCM-41 was found to exhibit the best activity and almost complete selectivity to glycerol carbonate (GC). Although, non-catalytic glycerol carbonylation resulted in GC formation but glycerol conversion achieved was twice with Zn/MCM-41 as a catalyst. Further to that increase in Zn loading from 2 to 5% resulted in increase in glycerol conversion from 63 to 82%. The prepared catalysts were characterized by XRD, NH 3 and CO 2 -TPD and effects of reaction parameters such as catalyst loading, glycerol to urea mole ratio and temperature on glycerol conversion and GC selectivity in batch mode of operation were also studied. Time on stream activity of 5% Zn/MCM-41 catalyst for continuous carbonylation of glycerol was also studied for *100 h with an average conversion of *55% and complete selectivity to GC. This indicated five times lower productivity of GC per h due to lower residence time than that in a batch operation as compared to that of a continuous operation. Activation energy estimated from the Arrhenius plot was found to be 39.82 kJ mol -1 suggesting that the reaction is kinetically controlled. A reaction pathway mediated by acid and basic sites of the Zn/MCM-41 catalyst is also proposed.

Direct one-pot hydrogenation of furfural (FFR) to cyclopentanone (CPO) was investigated over different silica-supported Pd catalysts. Among these, 4% Pd on fumed silica (4%Pd/f-SiO 2 ) showed remarkable results, achieving almost 98% furfural (FFR) conversion with ∼89% selectivity and 87% yield to cyclopentanone at 165 °C and 500 psig H 2 pressure. More interestingly, the fumed-silica-supported catalyst tuned the selectivity toward the rearrangement product, i.e., cyclopentanone, whereas all of the other supports were found to give ring hydrogenation as well as side chain hydrogenation products due to their parent Brönsted acidity and specific support properties. X-ray diffraction data revealed the presence of different phases of the face-centered cubic lattice of metallic Pd along with lowest crystallite size of 15.6 nm in the case of the silica-supported Pd catalyst. However, Pd particle size was found to be in the range of 5–13 nm with even dispersion over the silica support, confirmed by high-resolution transmission electron microscopy analysis. While studying the effect of reaction parameters, it was observed that lower temperature gave low furfural conversion of 58% with only 51% CPO selectivity. Similarly, higher H 2 pressure lowered CPO selectivity with subsequent increase in 2-methyl furan and ring hydrogenation product 2-methyl furan and 2-methyl tetrahydrofuran. Thus, as per the requirement, the product selectivity can be tuned by varying the type of support and/or the reaction parameters suitably. With the help of several control experiments and the characterization data, a plausible reaction pathway was proposed for the selective formation of cyclopentanone.

Glycerol transesterification using propylene carbonate (PC) to glycerol carbonate (GC) could be efficiently performed under solvent-free conditions using solid base as catalysts involving non-noble metal oxide in combination with hydrotalcites (HTs). Among all of the catalysts studied for transesterification, the best result was obtained over a calcium-doped hydrotalcite (Ca-HT) catalyst, giving 84% conversion of glycerol and almost complete GC selectivity. The crystal structure of HT was modified by incorporation of Ca and La into HT, as revealed by X-ray diffraction studies. The temperature-programmed desorption of carbon dioxide study confirmed the presence of the highest basic site density in terms of 1.94 mmol of CO 2 desorbed/g of catalyst, responsible for its higher transesterification efficiency of the Ca-HT catalyst. The Fourier transform infrared spectroscopy study showed peaks at 3036 and 3042 cm −1 for Ca-HT and lanthanum-doped hydrotalcite (La-HT), respectively, confirming the presence of hydrogen bonding between water and interlayer carbonate anions responsible for abstracting proton from the primary hydroxyl group of glycerol to attack over carbonyl carbon of PC. The presence of intercalated carbonate ions is also confirmed by the Raman study, in both HT and Ca-HT catalysts and even after use of the Ca-HT catalyst. The thermogravimetry−differential thermal analysis study evidenced the higher thermal stability of the Ca-HT (T 4 = 765 °C) catalyst than that of parent HT with a Mg/Al ratio of 3:1 (T 4 = 630 °C). Various process conditions, such as the temperature, molar ratio of glycerol/PC, and catalyst loading, significantly influenced conversion and selectivity of glycerol and GC, respectively.

Reacting glycerol with urea is the most attractive option for the production of glycerol carbonate (GC), as it utilizes two inexpensive chemicals readily available in the chemical cycle.

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Efficient and highly selective isomerization of glucose to fructose was achieved by using the inexpensive Ba−Zr mixed metal oxide catalyst. Catalyst was prepared by varying Ba−Zr ratios using co‐precipitation method. Various phases formed, planes exposed, morphology, elemental composition and particle size, basic site density and strength, oxidation state of elements were well studied by using various characterization techniques. The XRD analysis clearly indicates the presence of Ba+2 and Zr+4 in the form of BaO, ZrO2 and BaZrO3 phases. The SEM and HR‐TEM images indicate that, Ba−Zr (2 : 1) catalyst prepared showed uniform morphology with spherical and rod‐shaped particles ranging from 300 to 600 nm. Under the optimized reaction conditions Ba−Zr (2 : 1) catalyst exhibited excellent results in terms of 57 % of glucose conversion with 89 % selective formation of glucose. The presence of both acidic as well as basic sites play vital roles in activating the substrate molecules to selectively yield fructose. Ba−Zr (2 : 1) catalyst showed excellent recyclability performance up to four recycles.