The rapid expansion of shale gas development has revolutionized global energy markets, yet it has also introduced substantial environmental challenges, particularly concerning groundwater resources. This comprehensive review systematically examines the multifaceted impacts of shale gas extraction on groundwater, with a focus on contamination mechanisms, pollutant sources, and mitigation strategies. The study identifies key operational stages—exploration, drilling, hydraulic fracturing, and flowback—as potential sources of groundwater contamination. Inorganic pollutants, including heavy metals and radionuclides, as well as organic compounds such as hydrocarbons and chemical additives, are identified as primary contaminants. The review critically evaluates current wastewater treatment technologies, including reinjection, internal reuse, and advanced desalination methods, highlighting their efficacy and limitations. Additionally, the study proposes a refined environmental management framework that integrates wellbore integrity optimization, enhanced shale gas wastewater treatment, and stringent monitoring protocols. The adoption of clean fracturing technologies and renewable energy applications is recommended to minimize environmental footprints. By establishing comprehensive baseline data and robust pollution monitoring systems, this research provides a scientific foundation for sustainable shale gas development, ensuring the protection of groundwater resources. This review emphasizes the imperative of balancing energy security with environmental sustainability, offering actionable insights for policymakers, industry stakeholders, and environmental scientists.

Lost circulation in oil-based drilling fluids (OBDFs) remains difficult to mitigate because particulate lost circulation materials depend on bridging/packing and gel systems for aqueous media often lack OBDF compatibility and controllable in situ sealing. A dual-precursor oil–water biphasic metal–organic supramolecular gel enables rapid in situ sealing in OBDF loss zones. The optimized formulation uses an oil-phase to aqueous gelling-solution volume ratio of 10:3, with 2.0 wt% Span 85, 12.5 wt% TXP-4, and 5.0 wt% NaAlO₂. Apparent-viscosity measurements and ATR–FTIR analysis were used to evaluate the effects of temperature, time, pH, and shear on MOSG gelation. Furthermore, the structural characteristics and performances of MOSGs were systematically investigated by combining microstructural characterization, thermogravimetric analysis, rheological tests, simulated fracture-plugging experiments, and anti-shear evaluations. The results indicate that elevated temperatures (30–70 °C) and mildly alkaline conditions in the aqueous gelling solution (pH ≈ 8.10–8.30) promote P–O–Al coordination and strengthen hydrogen bonding, thereby facilitating the formation of a three-dimensional network. In contrast, strong shear disrupts the nascent network and delays gelation. The optimized MOSGs rapidly exhibit pronounced viscoelasticity and thermal resistance (~193 °C); under high shear (380 rpm), the viscosity retention exceeds 60% and the viscosity recovery exceeds 70%. In plugging tests, MOSG forms a dense sealing layer, achieving a pressure-bearing gradient of 2.27 MPa/m in simulated permeable formations and markedly improving the fracture pressure-bearing capacity in simulated fractured formations.

Oil-based drill cuttings (OBDCs) have received extensive attention for their environmental impacts and safe disposal. In this study, a high-performance sorbent material was prepared via the chelation and carbonization reaction for the high-value resource utilization of OBDCs. The coordination interaction between the organic acids and metal ions acted as a carbon source. Then, the metal elements were encapsulated into the formed carbon matrix. The results showed that the obtained composites exhibited abundant honeycomb-like pore structures. The addition of citric acid facilitated the formation of graphitized carbon materials and increased the specific surface area and surface functional groups. Impressively, the composites exhibited excellent adsorption performance for Cr(VI), with a maximum adsorption capacity of 56.84 mg/g. The adsorption process followed the pseudo-second-order kinetic model, and was mainly dominated by chemical adsorption. The excellent adsorption properties were attributed to the unique properties of the prepared carbon-based composites, including their large surface area, numerous pore structures, and abundant surface functional groups. This study provides new ideas related to the resource utilization of hazardous organic waste.