Graphitic carbon nitride (g-C₃N₄), with facile synthesis, unique structure, high stability, and low cost, has been the hotspot in the field of photocatalysis. However, the photocatalytic performance of g-C₃N₄ is still unsatisfactory due to insufficient capture of visible light, low surface area, poor electronic conductivity, and fast recombination of photogenerated electron-hole pairs. Thus, different modification strategies have been developed to improve its performance. In this review, the properties and preparation methods of g-C₃N₄ are systematically introduced, and various modification approaches, including morphology control, elemental doping, heterojunction construction, and modification with nanomaterials, are discussed. Moreover, photocatalytic applications in energy and environmental sustainability are summarized, such as hydrogen generation, CO₂ reduction, and degradation of contaminants in recent years. Finally, concluding remarks and perspectives on the challenges, and suggestions for exploiting g-C₃N₄-based photocatalysts are presented. This review will deepen the understanding of the state of the art of g-C₃N₄, including the fabrication, modification, and application in energy and environmental sustainability.

The extraction and collection of crude oil will result in the formation of numerous complex emulsions, which will not only decrease crude oil production, raise the cost of extraction and storage, and worsen pipeline equipment loss, but also seriously pollute the environment because the oil in the emulsion can fill soil pores, lower the soil’s permeability to air and water, and create an oil film on the water’s surface to prevent air–water contact. At present, a variety of demulsification technologies have been developed, such as physical, chemical, biological and other new emulsion breaking techniques, but due to the large content of colloid and asphaltene in many crude oils, resulting in the increased stability of their emulsions and oil–water interfacial tension, interfacial film, interfacial charge, crude oil viscosity, dispersion, and natural surfactants have an impact on the stability of crude oil emulsions. Therefore, the development of efficient, widely applicable, and environmentally friendly demulsification technologies for crude oil emulsions remains an important research direction in the field of crude oil development and application. This paper will start from the formation, classification and hazards of crude oil emulsion, and comprehensively summarize the development and application of demulsification technologies of crude oil emulsion. The demulsification mechanism of crude oil emulsion is further analyzed, and the problems of crude oil demulsification are pointed out, so as to provide a theoretical basis and technical support for the development and application of crude oil demulsification technology in the future.

Four products were obtained from sodium dodecylbenzene sulfonate (SDBS) and formaldehyde (40% solution) using a simple reaction. The products were characterized by TGA, IR, UV and MS to confirm the major chemicals in each sample. The new products could reduce the interfacial tension between oil and water in the experimental temperature range further compared to SDBS. The emulsion ability was also enhanced by SDBS-1 to SDBS-4. The oil-displacement efficiencies of SDBS-1 to SDBS-4 were obviously higher than that of SDBS, and the oil-displacement efficiency of SDBS-2 was the best, with an efficiency of 25%. The experimental results all indicate that these products have an excellent ability to reduce oil–water interfacial tension and that they can be used in the oil and petrochemical industry for oil production and have certain practical uses.

At present, the research on aquathermolysis catalysts mainly focuses on the catalytic effect of external catalysts on the reaction, ignoring the fact that external catalysts will form complexes with in situ inorganic minerals after entering the reservoir. In this paper, we investigated the effects of transition metal complexes as external catalysts and bentonite as in situ catalysts on aquathermolysis, respectively. Meanwhile, the aquathermolysis reaction co-catalyzed by external and in situ catalysts was further investigated. The results show that the transition metal complexes exhibited good co-catalysis with bentonite. The viscosity reduction rate can reach 73.47% at 200 °C and 4 h with 0.1 wt.% of catalyst (NAD–Zn) addition. The addition of ethanol under the same reaction conditions will further increase the viscosity reduction rate to 84.59%. The results of thermogravimetric analysis, component analysis and boiling range analysis of heavy oil show that the heavy components in heavy oil are cracked into light components after the aquathermolysis. The results of elemental analysis show that the heteroatoms in the heavy oil were removed and the quality of the crude oil was improved. The results of GC–MS analysis of the model compounds showed that the process of aquathermolysis was mainly through the cleavage of C–C, C–N and C–S bonds to crack the macromolecules into small molecules, and then achieve the effect of viscosity reduction. The main mechanism of catalyst action is the acidic center on the surface of the bentonite and the coordination bonds formed by the transition metal complexes with the heteroatoms.

To study the synergistic catalysis of an ex situ catalyst and in situ clay in the aquathermolysis of heavy oil, in this paper, a series of bentonite-supported catechol-metal complexes were prepared, and the catalytic viscosity reduction performance in the aquathermolysis of heavy oil was investigated. Under the optimized conditions, the viscosity can be reduced by 73%, and the pour point can be lowered by 15.0 °C at most, showing the synergistic catalysis of the ex situ catalyst and in situ clay in this aquathermolytic reaction. Thermogravimetry, physical adsorption-desorption, and scanning electron microscopy were conducted to characterize the thermal stability and microstructure of the ex situ catalyst. The components of the heavy oil before and after the reaction were fully characterized. Six model compounds were used to simulate the aquathermolysis reaction process. In order to study the mechanism of viscosity reduction after the catalytic aquathermolysis reaction, the compounds were analyzed by GC-MS. It is believed that these results will be beneficial in the future for related research in this field.

Oil is the “blood” and economic lifeblood of modern industry, but traditional light crude oil has been over-consumed, and it has been difficult to meet human demand for energy, so the exploitation of heavy oil is particularly important. In this paper, an oil-soluble catalyst was synthesized to catalyze the pyrolysis reaction of heavy oil in collaboration with reservoir minerals, so as to achieve efficient viscosity reduction of heavy oil and reduce production costs. The experimental results showed that Zn(II)O + K had the best synergistic viscosity reduction effect after the aquathermolysis of No. 1 oil sample under the reaction conditions of 180 °C, 4 h, 30% of water, and 0.2% of catalyst, respectively, and the viscosity reduction rate was 61.74%. Under the catalysis of the isopropanol system, the viscosity reduction rate was increased to 91.22%. A series of characterizations such as freezing point, thermogravimetric analysis, DSC analysis, component analysis, gas chromatography, wax crystal morphology analysis, and GC-MS analysis of aqueous organic matter were carried out on heavy oil after reaction by different reaction systems, and it could be verified that the viscosity of heavy oil was reduced. Finally, through the study of the reaction mechanism of the model compound, combined with the aqueous phase analysis, it can be clearly found that the depolymerization between macromolecules, the breaking of heteroatom chains, hydrogenation, ring opening, and other effects mainly occur during the reaction, thereby weakening the van der Waals force and hydrogen bond of the recombinant interval, inhibiting the formation of grid structure in heavy oil and effectively reducing the viscosity of heavy oil.