Search Results (1,198)

The development of all-concrete liquefied natural gas (LNG) storage tanks is hindered by the susceptibility of conventional concrete to ultra-low temperature (ULT) cycling down to −70 °C. While redispersible polymer powder (RPP) and polypropylene (PP) fibers individually enhance performance, their combined effect in various mineral admixture systems remains unclear. This study investigates the synergy and selective compatibility in hybrid-modified concrete containing fly ash (FA), silica fume (SF), or slag (SG). Comprehensive assessments after 50 ULT cycles reveal that the efficacy of hybrid modification is intrinsically governed by the mineral admixture. Among all systems, the silica fume-based hybrid system (EPSF) exhibits the highest residual compressive strength (57.5 MPa), the lowest strength loss (6.7%), and the most balanced durability. Microstructural analysis reveals that this synergy arises from a dense matrix, continuous polymer network, and effective fiber bridging—achieved only when the mineral admixture enables uniform RPP distribution. In contrast, the FA system exhibits a strength–durability trade-off, with RPP localized at interfaces, while the SG system shows a polymer-activated hydration mechanism. Microstructural and nano-mechanical analyses confirm that RPP acts as a pore filler in cement, an interfacial modifier in FA, a cohesive network former in SF, and a hydration activator in SG. This work establishes that superior ULT resilience requires not merely additive modifications but a matrix-enabled synergy, providing a scientific basis for the rational design of cryogenic concrete. Full article

Accurate prediction of CO₂ diffusion in multicomponent fluids is crucial for efficient enhanced oil and gas recovery (EGR) and carbon capture, utilization and storage (CCUS) operations. Conventional experimental methods struggle to accurately reproduce diffusion processes under reservoir conditions and provide limited insight into molecular-scale mechanisms. Therefore, a detailed microscopic understanding of CO₂ diffusion in complex fluids is urgently needed. In this study, the diffusion behavior and underlying mechanism of the CO₂-CH₄-H₂O system under reservoir temperature and pressure conditions were explored using both experimental techniques and molecular dynamics (MD) simulations. The results indicate that at 354.15 K, the diffusion coefficients follow the order D_CH4 > D_CO2 > D_Fick and decrease with increasing pressure. Higher CO₂ concentrations and water content lead to a reduction in D_CO2. Gravity exhibits a relatively minor influence, slightly enhancing D_CO2 while marginally reducing D_CH4. Near the critical point, a significant decrease in the thermodynamic factor indicates drastic changes in thermodynamic properties. Furthermore, the presence of water promotes CO₂ enrichment at the gas-water interface, consequently reducing both D_CO2 and D_CH4. This work provides valuable insights into bulk-phase transport in multicomponent aquifer systems under reservoir conditions and offers theoretical support for optimizing gas injection strategies and improving the efficiency of EGR and CCUS processes. Full article

As global oil and gas exploration extends to deep and ultra-deep formations, high-temperature and high-salt environments have become major challenges for drilling fluid viscosifiers. In this study, a hydrophobic associative polymer viscosifier, HATA, was synthesized via free-radical copolymerization using acrylamide (AM), 2-acrylamido-2-methylpropanesulfonic acid (AMPS), sodium styrene sulfonate (SSS), and stearyl methacrylate (SMA) as monomers, and its structure was systematically characterized, while its performance and action mechanism in a 4 wt% bentonite base slurry were evaluated. The results show that the base slurry modified with 3 wt% HATA maintains an apparent viscosity retention ratio of 69.20% following 16 h of hot rolling at 180 °C, with an API filtration loss of only 7.2 mL, and its HTHP filtration loss is 73.72% lower than that of the blank bentonite slurry system; this viscosifier sustains effective viscosity and yield point of the drilling fluid system at 200 °C and in 36 wt% NaCl brine. HATA achieves viscosity enhancement and filtration control by regulating surface charges of bentonite particles, constructing stable three-dimensional networks, and stabilizing clay hydration layers, thus presenting a high-performance viscosifier formulation for high-temperature and high-salinity water-based drilling fluids with important theoretical and engineering application values. Full article

The exceptional stability of C-F bonds renders PFAS highly persistent in aqueous environments, posing significant challenges for conventional treatment technologies. While plasma-based technologies show promise, their efficiency is often limited by poor gas–liquid mass transfer in bulk liquid. Here, an in-house constructed ultrasonic atomization–dielectric barrier discharge (UEN-DBD) system was developed to promote PFAS degradation under non-thermal plasma conditions. Ultrasonic atomization generated microdroplets, which promoted PFAS enrichment at the surface of microdroplets and facilitate interactions with plasma-generated reactive species. Using perfluorooctanoic acid (PFOA) and perfluorooctanesulfonate (PFOS) as model compounds, degradation behavior was evaluated over an initial concentration range of 0.01–1.0 ppm. At 0.01 ppm, degradation efficiencies of 96.06% for PFOA and 94.86% for PFOS were achieved within 5 min. Electron paramagnetic resonance (EPR) spectroscopy confirmed the formation of oxidative radicals (·OH) and suggested a mixed redox environment involving reactive species, potentially including superoxide (O₂·⁻) or hydrated electrons (e_aq⁻), in the discharge-treated system. High-resolution mass spectrometry results are consistent with a stepwise chain-shortening pathway dominated by successive –CF₂– scission, while fluoride-release measurements provided supporting evidence for partial defluorination. These findings advance the understanding of plasma-assisted PFAS degradation at the gas–liquid interface and provide a basis for the further development of plasma-assisted PFAS treatment strategies. Full article

The management of hazardous municipal solid waste incineration (MSWI) residues represents a critical challenge for sustainable development due to their increasing generation and environmental risk. At the same time, the cement industry faces urgent pressure to reduce CO₂ emissions associated with clinker production, creating a demand for alternative supplementary cementitious materials. The aim of this study was to evaluate the feasibility of valorising hazardous municipal solid waste incineration (MSWI) air pollution control fly ash (EWC 19 01 07*) as a constituent of Portland composite cement, in line with circular economy principles and the need to reduce CO₂ emissions associated with clinker production. The investigated fly ash, originating from flue gas cleaning processes, is characterised by high alkalinity and elevated concentrations of heavy metals, which currently necessitate controlled landfilling. To enable its safe reuse, the ash was subjected to high-temperature thermal treatment following granulation and subsequently incorporated into cement formulations under semi-industrial conditions. Two Portland composite cements were produced with different ash contents, corresponding to CEM II/A-07 and CEM II/B-07, while a Portland cement manufactured from the same clinker was used as a reference material. The chemical and phase composition of the ash before and after thermal treatment was analysed using XRF and XRD, supported by SEM/EDS observations. The results demonstrate that thermal treatment at 1150 °C induces partial phase stabilisation of APC fly ash without full vitrification, allowing its integration into cement systems under semi-industrial conditions. The incorporation of ash significantly alters hydration behaviour through increased water demand governed by particle porosity, CaO-rich phase composition, and early ionic interactions in the pore solution, leading to reduced workability and mechanical performance. While immobilisation efficiencies exceeding 99.5% were achieved for most heavy metals due to precipitation and incorporation into hydration products, barium exhibited persistent leaching controlled by its solubility under highly alkaline conditions and limited incorporation into C–S–H phases. These findings define both the technological feasibility and the key environmental constraints of APC fly ash utilisation in Portland composite cement. From a sustainability perspective, the proposed approach contributes to the reduction in hazardous waste landfilling and supports clinker substitution in cement production. The results demonstrate the potential of integrating waste management and low-carbon material design within a circular economy framework while highlighting current environmental limitations related to barium leaching. Full article

Konjac glucomannan (KG) is a biocompatible polysaccharide with limited functional performance in its native form, motivating modification strategies to enhance its properties. This study investigates the effect of gallic acid (GA) functionalization on the structural, physicochemical, mechanical, antioxidant, and biological properties of KG-based films. FTIR analysis confirmed that GA interacts with KG primarily through non-covalent hydrogen bonding without disrupting the polymer backbone. Modification with GA enabled concentration-dependent tuning of surface energy, roughness, hydration behavior, and water vapor permeability. Mechanical testing revealed a significant increase in stiffness and tensile strength accompanied by reduced elongation at higher GA contents. Antioxidant activity was markedly enhanced even at low GA concentrations. All films exhibited excellent hemocompatibility, while cytocompatibility toward human fibroblasts depended on GA content. Optical analysis indicated moderate color changes without severe discoloration. Overall, GA functionalization effectively improves the functional performance of KG films while preserving polymer integrity. Hence, GA-modified KG films as promising candidates for biomedical applications (like wound dressing) requiring antioxidant activity, controlled hydration, and biocompatibility. Full article

Water-based drill cuttings generated during onshore natural gas development are complex solid wastes that may pose environmental risks if improperly managed. This study evaluates the feasibility of reutilizing water-based drill cuttings as pavement base materials after stabilization using a novel composite stabilizer composed of cement, stabilizer liquid agent, and water-reducing powder (CLP stabilizer). Mix proportion optimization was conducted through compaction and 7-day unconfined compressive strength tests, followed by evaluation of road performance, including strength, compressive rebound modulus, water stability, and temperature shrinkage, with stabilized powder stabilized soil as a control. Microstructural characteristics were analyzed using X-ray diffraction and scanning electron microscopy, and environmental safety was assessed through heavy metal leaching tests and background soil investigation. The results show that the optimal mixture ratio of curing agent (5% cement + 2% liquid stabilizer + 8% superplasticizer powder) satisfies the strength requirement for pre-drilling road bases, exhibiting superior performance compared to the control group. When the stabilizer dosage reaches 9%, the 7-day unconfined compressive strength achieves a maximum of 3.38 MPa, representing a 51% increase over the control group. At a stabilizer dosage of 12%, the splitting tensile strength reaches a peak value of 0.901 MPa, showing a 60.3% improvement. These results indicate enhanced deformation resistance, water stability, and reduced temperature shrinkage rates. Microstructural analysis indicates that the formation of calcium silicate hydrate (C-S-H) gel and ettringite (AFt phase) leads to a denser structure and enhanced durability. Heavy metal concentrations comply with relevant standards, demonstrating controllable environmental risks and supporting sustainable pavement base application. Full article

The efficient utilization of industrial waste (containing alkaline compounds, especially Ca-based species) for flue gas desulfurization (FGD) is of great importance for both environmental protection and resource recovery. In this study, paper industry white mud was modified with Ca(OH)₂ to develop a cost-effective sorbent with enhanced SO₂ removal performance. Optimization experiments identified the best preparation conditions as a 1:1 Ca(OH)₂/white mud ratio, 60 °C modification temperature, 6 h reaction time, and a liquid-to-solid ratio of 3:1. Under these conditions, the sorbent achieved nearly 100% SO₂ removal in the first 6 h and maintained >90% efficiency after 10 h, significantly outperforming raw white mud and Ca(OH)₂ alone. Characterization revealed that the superior performance originated from structural stability and abundant active sites. BET analysis showed a high surface area (24.8 m²·g⁻¹) and pore volume (0.160 cm³·g⁻¹), which were largely preserved after desulfurization, indicating resistance to pore blockage. SEM images confirmed a transition from porous aggregates to densified product layers, consistent with a shrinking-core/product-layer mechanism. XRD identified CaSO₄·2H₂O as the dominant product, while in situ FTIR demonstrated that O₂ promotes sulfite oxidation and H₂O accelerates hydrated sulfate formation, enhancing activity but causing faster pore blocking. The presence of NO extended sorbent durability by catalyzing continuous sulfite oxidation through NO/NO₂ redox cycling. Overall, Ca(OH)₂-modified white mud combines high reactivity, durability, and structural stability, offering a promising alternative to conventional sorbents. This work provides a viable route for the resource utilization of paper industry waste and practical insights for designing efficient and sustainable materials for industrial FGD systems. Full article

Background: Polysubstance use, particularly the combination of opioids and stimulants, represents a growing public health concern due to its high risk of severe multisystem complications and mortality. Here, we present a case illustrating the lethal synergy of opioid–stimulant co-use. Methods: A 37-year-old male with chronic Hepatitis C and documented polysubstance use reported recent use of fentanyl, cocaine, methamphetamine, and cannabis. He presented with generalized weakness, left lower limb pain, tense edema, and anuria. Clinical assessment included monitoring of vital signs, physical examination, capillary blood gas analysis, extended laboratory panels (muscle and cardiac enzymes, electrolytes, and coagulation parameters), urinalysis, and Doppler imaging. Management over five days included intravenous hydration, diuretics, urinary alkalinization, electrolyte correction, anticoagulation, metabolic and vitamin therapy, hemodialysis, and comprehensive supportive care. Results: Laboratory evaluation revealed massive rhabdomyolysis (peak CK 161,050 U/L), severe hyperkalemia (K⁺ 8.4 mmol/L), metabolic acidosis, acute kidney injury with oligoanuria, and left-sided deep vein thrombosis. Despite intensive multidisciplinary interventions, the patient’s repeated refusal of ongoing treatment critically contributed to a fatal outcome. Conclusions: This case underscores the high mortality risk associated with opioid–stimulant co-use and the crucial impact of treatment refusal. Clinicians and public health stakeholders should recognize the rapid progression of multisystem dysfunction in polysubstance users and prioritize early, aggressive interventions combined with patient engagement strategies to mitigate fatal outcomes. Full article

Supersulfated cement (SSC) is an environmentally friendly cementitious material with a low clinker content, in which industrial byproduct gypsum serves as the sulfate source, thereby enabling the valorization of solid waste. The hydration process, pore structure, microstructure, and hydration products were investigated using paste samples by means of isothermal calorimetry, X-ray diffraction (XRD), thermogravimetric analysis (TG–DTG), Fourier transform–infrared spectroscopy (FT-IR), mercury intrusion porosimetry (MIP), and scanning electron microscopy (SEM), while compressive strength was evaluated using mortar specimens. Compared with ordinary Portland cement (OPC), SSC offers clear advantages in reducing energy consumption and greenhouse gas emissions. In this study, the effects of titanium gypsum (TG) and flue gas desulfurization gypsum (FGD) on the hydration behavior, fluidity, mechanical properties, and microstructural evolution of an anhydrite (AH)–phosphogypsum (PG)-based SSC were systematically investigated. The results indicate that the incorporation of 11% TG and FGD mitigates the strong sulfate environment caused by the rapid dissolution of soluble AH, thereby regulating the hydration process. As the proportion of TG and FGD increased, the cumulative heat release within 72 h gradually decreased. When AH was completely replaced, the cumulative heat release of TG4 and FG4 decreased by approximately 19.7% and 28.6%, respectively. TG and FGD exhibited opposite effects on the fluidity of SSC while both promoting strength development. Among all mixtures, TG2 and FG2 showed the best performance, with the highest 28-day compressive strengths of 50.15 MPa and 51.95 MPa, respectively. Microstructural analysis reveals that differences in particle size distribution and dissolution kinetics among gypsums governed the sulfate release characteristics and slag activation mechanisms, thus leading to distinct hydration pathways, pore structure evolution, and microstructural densification. This study provides a theoretical basis for the efficient utilization of various industrial byproduct gypsums and offers important guidance for the controllable design of SSC performance. Full article

With the expansion of global oil and gas resource exploration and development into deep and ultra deep layers, the efficient development of deep carbonate rock fracture cave reservoirs has become the key to ensuring energy security. However, this type of reservoir commonly faces high temperatures, high salinity, and extremely strong heterogeneity, leading to increasingly severe water content spikes caused by dominant water flow channels. Although the existing traditional inorganic plugging agent has good temperature resistance, it has the defects of great brittleness and easy cracking, while the organic polymer gel is prone to degradation failure under high temperature and high salt environments. In order to solve the above problems, a new biochar-enhanced inorganic composite gel system was constructed by using biochar prepared from agricultural and forestry waste pyrolysis as a functional enhancement component. Through rheological testing, high-temperature and high-pressure mechanical experiments, long-term thermal stability evaluation, and dynamic sealing experiments of fractured rock cores, the reinforcement and toughening laws and rheological control mechanisms of biochar on inorganic matrices were systematically studied. Research has found that a biochar content of 0.5 wt% can significantly improve the micro pore structure of the matrix. By utilizing its micro aggregate filling effect and interfacial chemical bonding, the compressive strength of the solidified body can be increased to over 2 MPa, and there is no significant decline in strength after aging at 130 °C for 30 days. More importantly, the unique “adsorption slow-release” mechanism of biochar effectively stabilizes the hydration reaction kinetics at high temperatures, extending the solidification time of the system to 15 h and solving the problem of flash condensation in deep well pumping. This system exhibits excellent shear thinning characteristics and crack sealing ability, and presents a unique “yield reconstruction” toughness sealing feature. This study elucidates the multidimensional strengthening mechanism of biochar in inorganic cementitious materials, providing technical reference for stable oil and water control in deep fractured reservoirs. Full article

The Midong Block is currently a primary target for coalbed methane (CBM) exploration and development in Xinjiang. However, fracturing operations in this region generally exhibit low flowback rates, which escalate the risk of reservoir damage and ultimately suppress daily gas production. To elucidate the impact of various geological and engineering factors on flowback efficiency and permeability damage, as well as their underlying mechanisms, this study conducted fracturing fluid flowback simulation experiments. The pulse-decay permeability measurement and weighing methods were employed to quantify the variations in flowback rates and permeability damage intensities under different conditions. Experimental results indicated that the permeability damage rate in the Xishanyao Formation coal samples ranged from 3.12% to 92.86% after flowback, with 92% of the samples exhibiting a flowback rate of less than 10%. This significant impairment was primarily attributed to the synergistic effects of stress-induced fracture closure, clay mineral hydration swelling, and coal fines migration. Specifically, elevated confining pressures and prolonged soaking times exacerbated reservoir damage. A low flowback pressure differential intensified the water locking effect, hindering fluid recovery. Notably, the flowback velocity displayed a U-shaped velocity sensitivity profile. In the low-temperature regime, damage characteristics fluctuated, controlled by competitive thermal–hydro–mechanical (THM) coupling mechanisms. Full article

Wellbore stability is one of the major challenges during drilling operations in shale gas formations. Drilling fluid seepage can significantly alter the pore pressure around the wellbore, thereby inducing wellbore instability. In this study, the Darcy pore fluid flow model was applied to both the mud cake and wellbore to predict pore pressure, which helps improve the accuracy of calculating collapse pressure and fracture pressure. Shale samples were collected from the Puguang Gas Reservoir, and their composition and physicochemical properties were systematically analyzed. The results indicate that the clay content in the formation can reach up to 35.5%, with distinct hydrophilic characteristics, and the maximum hydration expansion rate of the shale is 5.79%. The permeabilities of shale and mud cake were measured via the pore pressure transmission test. Specifically, shale samples from Sub-layer 1 exhibit the highest permeabilities for both rock and mud cake, which are 8.27 × 10⁻¹⁸ m² and 2.07 × 10⁻²⁰ m², respectively. In contrast, samples from Sub-layer 3 show the lowest permeability values, being 2.76 × 10⁻²⁰ m² and 1.66 × 10⁻²² m². The borehole tensile breakdown pressure and compressive collapse pressure were calculated using a poro-mechanical coupling model. The Sub-layer with the lowest cohesion strength after drilling fluid immersion presents the narrowest mud density window of 0.04 g/cm³, making it the most susceptible to wellbore stability failures; furthermore, the maintenance of wellbore stability requires strict control of the drilling mud density within the range. This study can provide guidance for accurate prediction of mud density window during drilling operations in shale formations. Full article

Fluid seepages and seabed pockmarks are widely observed on continental margins worldwide in hydrate- and non-hydrate-bearing sediment. Subsurface gas chimneys connecting seafloor pockmarks to underlying gas reservoirs are commonly revealed by seismic reflection data, indicating pathways of past and present fluid migration. Fluid seepage occurs when the seal of a gas reservoir is breached, allowing fluids to migrate upward and vent at the seafloor, forming pockmarks. In hydrate-bearing settings, gas reservoirs beneath hydrate layers typically consist of coexisting water and gas phases. However, quantitative constraints on gas saturation in free-gas zones beneath hydrates inferred from pockmark morphology remain limited. In this study, a two-phase pockmark model was developed to investigate gas-chimney growth and pockmark formation, and to estimate gas saturation in free-gas zones below hydrates using pockmark depth and gas-zone thickness as key parameters. The model was applied to the Storegga Slide region off Norway, where hydrates, pockmarks, and chimney-like seismic anomalies have been documented. Here, the application is intended to represent localized near-threshold (pre-seepage) conditions leading to pockmark initiation, rather than the present-day post-venting state. Model results for the initiation (near-threshold, pre-venting) stage indicate that the effective gas saturation in the free-gas reservoir beneath the hydrates was approximately 1.36–1.58% for gas-zone thicknesses of 50–100 m, and that the corresponding chimney-propagation timescale during initiation was on the order of ~200 years. These estimates represent threshold conditions required for seal breach and pockmark formation rather than present-day seepage states. During venting, methane gas may form hydrates within the chimney inside the hydrate stability zone, while authigenic carbonates precipitate in pockmarks and shallow sediments. These secondary hydrates and carbonates eventually seal the chimney, leaving behind a residual gas chimney in the subsurface sediment. Full article

Natural gas hydrates, as an abundant potential energy resource, are widely present in marine sediments. In this paper, a novel method using color recognition technology is proposed for reconstructing marine hydrate reservoirs. By identifying the red, green, and blue values of image colors within the study area’s grid, numerical values are assigned and translated into geological parameters. These parameters are then input into the Computer Modeling Group software to establish heterogeneous reservoirs, and numerical simulations are conducted. The results indicate that this method successfully establishes a correspondence between color features and geological parameters. The reconstructed model images exhibit a high degree of consistency with the original images, allowing for precise parameter readings. The method was applied to hydrate reservoirs in the second trial production area of the South China Sea, the Shenhu SH2 area, and the Nankai Trough. The cumulative gas production obtained through numerical simulation of the reconstructed models closely matched the known production data, with discrepancies of 3.5%, 0.9%, and 7.6%, respectively. These findings confirm the reliability of the model, providing valuable insights for future studies on heterogeneous hydrate reservoirs and extending its application prospects to heterogeneous oil and gas reservoir research. Full article