The Bio-oil was produced from the pyrolysis of agricultural wastes (Eucalyptus sawdust) and discarded soybean frying oil. The temperature of the pyrolysis system was initiated at 28°C and increased to 850°C. Atmospheric distillation of crude bio-oil was performed and a fraction at a temperature range 160–240°C (pyrolysis oil) was separated and subjected to GC-MS, ¹H-NMR, TGA and FTIR analysis to identify the different properties and compounds present in pyrolysis oil. It was noticed that there was an abundance of oxygen and nitrogen containing compounds as well as other reactive species in pyrolysis oil. To reduce the amount of these species, the pyrolysis oil was subjected to hydrogenation in the presence of NiMo as a catalyst. After hydrogenation, the atmospheric distillation of hydrogenated bio-oil was performed and another fraction at temperature range 160–240°C (hydrogenated bio-oil) was separated and analyzed by the same techniques. It was noticed that during hydrogenation, more than 60% oxygenated and other reactive species were converted into hydrocarbons. Hydrogenated bio-oil showed very similar physico-chemical properties such as distillation curve, density, viscosity, freezing point, flash point, the presence of hydrocarbons and enthalpy of combustion as aviation kerosene also known as QAV-1.

Titanium dioxide (TiO₂) has been widely used as a potential candidate for the production of green hydrogen using the artificial photosynthesis approach. However, the wide bandgap (∼3.3 eV) of anatase TiO₂ makes it difficult to absorb a large fraction of the solar radiation reaching the Earth, thus providing a low photocatalytic activity. Anatase TiO₂ absorbs only 4% of solar radiation, which can be improved by engineering its bandgap to enhance absorption in the visible region. In the literature, many strategies have been adopted to improve the photocatalytic activity of TiO₂, such as metal and non-metal doping and heterojunctions. These techniques have shown incredible enhancement in visible light absorption and improved photocatalytic activity due to their ability to lower the bandgap of pure TiO₂ semiconductors. This review highlights different techniques like doping, heterojunctions, acidic modification, creating oxygen vacancies, and temperature- and pressure-dependence, which have improved the photochemical response of TiO₂ by improving charge-transfer efficiencies. Additionally, the charge-transfer mechanism and enhancement in the photochemical response of TiO₂ is discussed in each portion separately.

This work presents the production of sewage sludge oil by pyrolysis, shows the physicochemical properties and compares it with commercial diesel. The sewage sludge was dried and mixed to discarded cooking oil to increase the fuel conversion rate due to the pyrolysis process at an initial temperature of 25 °C and a final of 650 °C. The oil was distilled and analyzed in a Proton nuclear magnetic resonance (1H-NMR), Gas Chromatogram and Mass spectrometry (GC-MS), thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR) to perform a structural characterization on the molecular distribution, groups of functions and the product thermal stability. The authors measured fundamental physicochemical properties like viscosity, density and flashpoint and compared the results with the corresponding commercial S-10 diesel properties observing good agreement.

Several Carbon Capture and Storage (CCS) techniques have been studied including injections of carbon dioxide (CO₂) into the mature and/or depleted hydrocarbon reservoirs and deep saline aquifers. This work aims to test storing CO₂ into the magnesium-rich evaporite strata and also into the stratigraphic intervals containing Mg-rich brines. The test simulates Mg-carbonation of the synthetic solution obtained from the Mg-evaporite mineral, bischofite – both experimentally in the laboratory condition and also through computerised geochemical simulation. The laboratory experiments, which resulted in the crystallisation of anhydrous magnesite, were analysed. The TOUGHREACT^TM, Geochemist’s Workbench^TM (GWB) and PHREEQC^TM software simulated the experiments as computerised geochemical model and tested the results for natural geological conditions. The geochemical simulations successfully demonstrate the immense CCS potential for the Mg-evaporite (as well as the sedimentary strata charged with Mg-evaporitic brine) at their subsurface geological occurrences at elevated pressure-temperature and high salinity.

Carbon capture and storage (CCS) has been observed as an alternative measure to mitigate emissions from greenhouse gases. CCS systems separate CO2 during the process of converting fuel and transport to the facilities where they are stored, e.g., under geological formation conditions. Capture and sequestration technologies are now widely used in different industries. CO2 capture is currently a costly and energy-consuming technology. The costs obviously depend on the size of the plant and the type of fuel used. Generally, capture systems are categorized into three categories: pre-combustion, post-combustion, and oxy-fuel combustion. The saline aquifer, depleted oil, and gas fields are large-capacity storage sinks. The coalbeds also provide as a substitute to geological storage. One of the main advantages of coal storage is renewable methane fuel and coal desulfurization. The studied coal reserves are located in Candiota, State of Rio Grande do Sul, Brazil. These are the largest coal deposits in the country, with a reserve of 1 billion tons. This work will represent a study on CO2 storage in Candiota coalbed system. The use of a synthetic CO2 cylinder with a flow of 0.2 L/min varies the time of contact with the coalbed. The results from the volatile matter increase by 11%. The results of the ultimate analysis exhibited an 8% increase for carbon and oxygen after 60 minutes of CO2 flow in the coalbed. On the other hand, there was a reduction of 32% for sulfur. The resultant phenomena occur due to the adsorption capacity of CO2, where the compounds are released from the pores of coal.

This work is based on our previous research on sulfur-assisted graphitization of biopitch by focusing on catalyst-driven optimization of biomass-derived pitch (BDP) composites as sustainable alternatives to coal tar pitch (CTP). Biomass from eucalyptus sawdust was pyrolyzed to produce BDP, which was used as a binder for carbon–carbon composites. The properties of BDP/graphite and CTP/graphite composites, including bending strength, electrical conductivity, hardness, density, porosity, mass loss, and shrinkage, were compared. Furthermore, the influence of catalysts (NiSO₄, K₂SO₄, CuSO₄, FeSO₄, and KOH) on composite performance was systematically investigated. Results show that catalyst selection significantly enhances structural, electrical, and mechanical properties, demonstrating the potential of combining eco-friendly materials with strategic catalyst engineering to develop high-performance, sustainable composites.