The hydrogenation of methyl linoleate to methyl oleate and methyl stearate was studied in a 6-inch stirred batch reactor at 121°C and 45 psia.
Hydrogenolysis of methyl formate was studied at atmospheric pressure over skeletal copper and copper chromite catalysts.
The gas phase condensation of formaldehyde with propionic acid, propionic anhydride, and methyl propionate was studied over a series of V-Si-P catalysts of varying atomic ratios.
The behaviour of a series of 4-substituted thiophenols as chain transfers in the photopolymerization of the acrylamide and methyl methacrylate was studied.
The steady-state rate of polymerization for the methyl methacrylate was studied first by carrying out the experiments at regular intervals of time with fixed concentrations of all other parameters.
Hydrodeoxygenation of methyl oleate was studied over Ni2P/SBA-15 in a fixed-bed reactor and showed that uniform dispersion of NiP on SBA-15 resulted in higher conversion of esters and selectivity of long-chain paraffin [16].
Photocatalytic activity of the as-prepared ZnO nanocrystals with various (0 0 2) orientations in degradation of methyl orange was studied, it was found that the exposed {0 0 1} facets are reactive facets.
Photocatalytic activity of porous ZnO nanosheets in degradation of methyl orange was studied, and the results indicate that the porous ZnO nanosheets show superior photoreactivity, compared to ZnO nanorods as a benchmarking material.
The electrochemical behaviour in DMF of sulphapyridine and its N1-methyl derivative was studied by means of polarographic, coulometric and cyclic voltammetric methods.
The formation of methyl methacrylate (MMA) was studied in a vapor-phase reaction between methyl propionate (MP) and methanol without using any sources of formaldehyde.
