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Methanol dehydration process to dimethyl ether (DME) has been considered as one of the main routes to produce clean fuel, that is, DME. Thus, efficient catalysts are highly required for selective production of DME. Herein, UiO-66 was used as a precursor for the synthesis of zirconium oxide sulfate embedded carbon (ZrOSO4@C). The synthesis method involves a one-step carbonization of UiO-66 in the presence of sulfuric acid (10 wt %). Material characterizations using X-ray diffraction, X-ray photoelectron spectroscopy, Fourier transform infrared, and Raman spectroscopy approve the formation of the high crystalline phase of ZrOSO4@C. Nitrogen adsorption–desorption isotherms and high-resolution transmission electron microscopy confirm the mesopore structure of the materials. Acidity analysis using pyridine temperature-programmed desorption and isopropanol dehydration corroborates that ZrOSO4@C has weak and intermediate acidic sites making ZrOSO4@C an effective catalyst for methanol dehydration to DME. The materials offered full conversion (100%) with excellent selectivity (100%) at a relatively low temperature (250 °C). The catalyst exhibited a long-term stability for 120 h. Based on these results, DME is produced efficiently in terms of conversion, selectivity, and long-term stability.

Oxidative coupling of CH4 forming C2H6 and C2H4 proceeded smoothly upon contact with Na2O2, BaO2, and SrO2 at low temperatures below 673 K. This indicates that O22− ions are very reactive for activation of CH4. O2− ions contained in the peroxides did not activate CH4.

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