Mesoporous carbon nitride supported MgO for enhanced CO2 capture.

The growing concern about the environmental consequences of anthropogenic CO2 emissions significantly stimulated the research of low-cost, efficient, and recyclable solid adsorbents for CO2 capture. In this work, a series of MgO-supported mesoporous carbon nitride adsorbents with different MgO contents (xMgO/MCN) was prepared using a facile process. The obtained materials were tested for CO2 capture from 10 vol% CO2 mixture gas with N2 using a fixed bed adsorber at atmospheric pressure. At 25 ºC, the bare MCN support and unsupported MgO samples demonstrated CO2 capture capacities of 0.99, and 0.74 mmol g-1, respectively, which were lower than those of the xMgO/MCN composites.The incorporation of MgO into the MCN improved the CO2 uptake, and the 20MgO/MCN exhibited the highest CO2 capture capacity of 1.15 mmol g-1 at 25 °C. The improved performance of the 20MgO/MCN nanohybrid can be possibly assigned to the presence of high content of highly dispersed MgO NPs along with its improved textural properties in terms of high specific surface area (215 m2g-1), large pore volume (0.22 cm3g-1), and abundant mesoporous structure. The efffects of temperature and CO2 flow rate were also investigated on the CO2 capture performance of 20MgO/MCN. Temperature was found to have a negative influence on the CO2 capture capacity of the 20MgO/MCN, which decreased from 1.15 to 0.65 mmol g-1with temperature rise from 25 C to 150º C, due to the endothermicity of the process. Similarly, the capture capacity decreased from 1.15 to 0.54 mmol g-1 with the increase of the flow rate from 50 to 200 ml minute-1 respectively. Importantly, 20MgO/MCN showed excellent reusability with consistent CO2 capture capacity over five sequential sorption-desorption cycles, suggesting its suitability for the practical capture of CO2.

Efficient CO2 methanation using nickel nanoparticles supported mesoporous carbon nitride catalysts.

The CO2 methanation technique not only gives a solution for mitigating CO2 emissions but can also be used to store and convey low-grade energy. The basic character and large surface area of mesoporous carbon nitride, (MCN), are considered promising properties for the methanation of CO2. So, a series (5-20 wt.%) of Ni-doped mesoporous carbon nitride catalysts were synthesized by using the impregnation method for CO2 methanation. the prepared catalysts were characterized by several physicochemical techniques including XRD, BET, FT-IR, Raman spectroscopy, TEM, TGA analysis, Atomic Absorption, H2-TPR, and CO2-TPD. The catalytic performance was investigated at ambient pressure and temperature range (200-500 °C) using online Gas chromatography system. The prepared catalysts showed good performance where 15%Ni/MCN exhibited the best catalytic conversion and methane yield with 100% methane selectivity at 450 °C for investigated reaction conditions.

Waste cooking oil processing over cobalt aluminate nanoparticles for liquid biofuel hydrocarbons production.

The catalytic conversion of waste cooking oil (WCO) was carried out over a synthetic nano catalyst of cobalt aluminate (CoAl2O4) to produce biofuel range fractions. A precipitation method was used to create a nanoparticle catalyst, which was then examined using field-emission scanning electron microscopy, X-ray diffraction, energy dispersive X-ray, nitrogen adsorption measurements, high-resolution transmission electron Microscopy (HRTEM), infrared spectroscopy, while a gas chromatography-mass spectrometer (GC-MS) was used to analyze the chemical construction of the liquid biofuel. A range of experimental temperatures was looked at including 350, 375, 400, 425, and 450 °C; hydrogen pressure of 50, 2.5, and 5.0 MPa; and liquid hour space velocity (LHSV) of 1, 2.5, and 5 h-1. As temperature, pressure, and liquid hourly space velocity increased, the amount of bio-jet and biodiesel fractional products decreased, while liquid light fraction hydrocarbons increased. 93% optimum conversion of waste cooking oil over CoAl2O4 nano-particles was achieved at 400 °C, 50 bar, and 1 h-1 (LHSV) as 20% yield of bio-jet range,16% gasoline, and 53% biodiesel. According to the product analysis, catalytic hydrocracking of WCO resulted in fuels with chemical and physical characteristics that were on par with those required for fuels derived from petroleum. The study's findings demonstrated the nano cobalt aluminate catalyst's high performance in a catalytic cracking process, which resulted in a WCO to biofuel conversion ratio that was greater than 90%. In this study, we looked at cobalt aluminate nanoparticles as a less complex and expensive alternative to traditional zeolite catalysts for the catalytic cracking process used to produce biofuel and thus can be manufactured locally, which saves the cost of imports for us as a developing country.