Search Results (784)

Background/Objectives: Clopidogrel is a widely prescribed antiplatelet prodrug that requires bioactivation, primarily by the polymorphic CYP2C19 enzyme. Genetic variation in this enzyme leads to differences in active metabolite formation and has prompted the development of pharmacogenetics-guided prescribing. However, current pharmacogenetic strategies are grounded in drug metabolism knowledge derived from mass balance studies conducted in small groups of healthy volunteers. This narrow evidence base may limit the data’s applicability to real-world settings, where factors like polypharmacy or altered organ function may influence drug response. Methods: Pharmacogenetics could benefit from real-world drug metabolism and excretion studies, which we conducted for clopidogrel in 38 kidney and 16 liver transplant recipients from the TransplantLines Biobank and Cohort Study (NCT03272841), utilizing existing LC-SWATH/MS pharmacometabolomic data. Clopidogrel-associated metabolic signals were identified using xenobiotic metabolism knowledge and literature-reported pathways. Results: Across both transplant groups, 26 clopidogrel-associated features were prioritized, of which some matched previously reported urinary metabolites, had previously been observed in plasma, or represented previously unreported metabolites. Clopidogrel carboxylic acid predominated in kidney transplant recipients, whereas its glucuronide form was most abundant in liver transplant recipients. Notably, unmetabolized clopidogrel was consistently detected across all patients. Moreover, our data support a thiol desulfurization route, aligning with emerging evidence of clopidogrel’s role as a hydrogen sulfide-releasing drug. Conclusions: More (putative) clopidogrel metabolites were detected than previously reported, demonstrating the value of pharmacometabolomics in expanding our understanding of drug metabolism. This approach provides novel data that may complement pharmacogenetics research to understand clopidogrel response variability among treated patients. Full article

To address global carbon reduction demands, oxy-fuel combustion in circulating fluidized beds (oxy-CFB) has emerged as a highly promising carbon capture technology, offering extensive fuel flexibility and facilitating bioenergy with carbon capture and storage (BECCS). However, its commercialization is hindered by significant energy penalties and complex scale-up challenges. This review comprehensively analyzes the fundamental multiphase mechanisms, heat transfer behaviors, and multi-pollutant emission characteristics of oxy-CFB systems, drawing upon multiscale modeling advancements and operational data from pilot to 30 MW_th industrial demonstrations. Replacing air with an O₂/CO₂/H₂O mixture fundamentally alters gas–solid hydrodynamics and char conversion pathways, necessitating active fluidization state re-specification. Despite shifting optimal desulfurization temperatures and introducing recarbonation risks, the technology demonstrates inherent advantages in synergistic pollutant control, including the complete elimination of thermal NO_x. While atmospheric oxy-CFB is technically viable, transitioning to pressurized operation is critical to minimizing system efficiency penalties. Furthermore, integrating oxygen carrier-aided combustion (OCAC) and developing advanced predictive control strategies are essential to managing multi-module thermal inertia and enabling rapid dynamic responsiveness for modern power grids. Full article

The Ordovician system in the Shunbei area of the Tarim Basin hosts typical ultra-deep, fault-controlled fracture–vuggy hydrocarbon reservoirs. Compared with the surrounding Tabei and Tazhong areas, the genetic types of Ordovician formation water in Shunbei are more complex, and the relationships and spatial distribution of oil, gas, and water exhibit strong heterogeneity and pronounced fault control. This study systematically collected formation water geochemical and pressure data to clarify the geochemical characteristics and origin of Ordovician formation water in the Shunbei area and to investigate the indicative relationships between ion concentrations and ionic ratios of formation water and reservoir dolomitization, hydrocarbon migration, and accumulation. Research shows that, in contrast to the Tabei and Tazhong areas, the Ordovician formation water in Shunbei is predominantly of the calcium chloride (CaCl₂) type, with enrichment in Ca²⁺ and depletion in Mg²⁺, which may be related to euhedral dolomitization. In fault-controlled fracture–vuggy reservoirs, a high desulfurization coefficient—contrary to its interpretation in conventional reservoirs—corresponds to favorable zones for hydrocarbon accumulation. The rare earth element (REE) composition of the formation water is characterized by heavy REE enrichment, a distinct negative cerium (Ce) anomaly, and a positive europium (Eu) anomaly. Combined with hydrogen–oxygen and strontium isotopic data, these features indicate that the Ordovician formation water in Shunbei represents original depositional paleoseawater that has undergone cross-formational flow and concentration. The water bodies are divided into two distinct formation water systems bounded by the Shunbei No. 5 fault zone. Favorable zones for hydrocarbon enrichment are controlled by source rock distribution, and hydrocarbons migrate together with formation water along strike-slip faults within the Shunbei area, showing a northwest-to-southeast trend. The region between the middle segments of the Shunbei No. 4 and No. 8 fault zones is identified as a favorable area for hydrocarbon accumulation. Full article

Liquid entrainment presents a significant challenge in wet flue gas desulfurization systems, leading to downstream corrosion and secondary pollution. This study systematically investigates the characteristics of liquid entrainment and pressure drop in a gas cyclone–liquid jet absorption separator (GLAS) through both experimental and simulation methods. The effects of inlet gas flow rate (Q_G), absorbent flow rate (Q_L), overflow pipe insertion depth, and the presence of a liquid-guiding cover (LGC) were evaluated. The results revealed that liquid entrainment initially increased and then decreased with rising Q_G, Q_L, and insertion depth of overflow pipe, given the competing effects of turbulent jet breakup and centrifugal separation. To mitigate liquid entrainment, a novel LGC was introduced at the overflow pipe outlet. This intervention resulted in a reduction in liquid entrainment by up to 23.9%, achieved through physical interception and inertial impaction, while maintaining the difference value of pressure drop of less than 302 Pa. The numerical simulations further analyzed the gas–liquid two-phase distributions in GLAS under various operating conditions, with results that align well with experimental observations. These findings offer valuable insights for mitigating liquid entrainment in GLAS and optimizing its industrial applications. Full article

Traditional calcium hydroxide (Ca(OH)₂) typically exhibits low specific surface area and reactivity, significantly limiting its efficacy in industrial gas–solid reactions such as flue gas desulfurization and thermochemical energy storage. To address these limitations, this study proposes a two-stage synthesis strategy designed to enhance the surface properties and chemical activity of Ca(OH)₂. The process involves the preparation of high-activity calcium oxide (CaO), followed by controlled hydration using diethylene glycol (DEG). Drawing on established mechanisms from cement chemistry, wherein potassium ions (K⁺) catalyze the decomposition of calcium carbonate (CaCO₃), limestone particles (10–20 mm) were pre-soaked in a 0.1 mol/L potassium nitrate (KNO₃) solution for 48 h prior to calcination. Characterization via X-ray diffraction (XRD), scanning electron microscopy (SEM), and Blaine Air Permeability Method analysis revealed that this pretreatment accelerated decomposition kinetics by inducing surface defects, yielding CaO with a maximum reactivity of 435.7 mL. Subsequent hydration at 80 °C with 70 wt% DEG effectively suppressed particle agglomeration and promoted the formation of thin platelet structures. The resulting Ca(OH)₂ achieved a utilization efficiency of 98.5% and a specific surface area of 43.24 m²/g, demonstrating a robust technical route for fabricating high-performance calcium-based sorbents for environmental and energy applications. Full article

A flexible polyionic liquid (PIL) nanofiber membrane-supported phosphomolybdic acid catalyst (PM-PIL) was fabricated via stepwise chemical transformation of polyacrylonitrile (PAN) nanofiber membranes. The nitrile groups of PAN were converted into pyridine units, followed by quaternization and anion exchange with phosphomolybdic acid (PMo), resulting in a polyionic liquid membrane with uniformly immobilized PMo species. Benefiting from its nanofibrous architecture and ionic liquid characteristics, the PM-PIL membrane simultaneously acts as a heterogeneous catalyst and a Pickering emulsion stabilizer, enabling efficient interfacial catalytic oxidation desulfurization. The PM-PIL membrane exhibited excellent catalytic performance toward dibenzothiophene (DBT) oxidation in an H₂O₂-based model oil system. Under optimized conditions (60 °C, O/S = 150:1), more than 90% DBT removal was achieved within 90 min, and complete desulfurization was obtained within 2 h. Compared with phosphomolybdic acid and poly(pyridine), the PM-PIL membrane showed markedly enhanced activity and stability, maintaining over 90% efficiency after six cycles. Product analysis confirmed selective oxidation of DBT to dibenzothiophene sulfone. This work provides a robust and recyclable membrane-based catalytic platform for efficient oxidative desulfurization. Full article

Soil salinization is a major challenge affecting crop yield in arid and semi-arid regions. Amendments to agricultural soil under drip irrigation represent a potential strategy to ameliorate soil salinization. This study conducted a field experiment over two years to identify the impacts of desulfurized gypsum, biochar, and straw on sunflower yield and soil characteristics in salinized and alkalized soil. Soil amelioration significantly improved soil characteristics by reducing saline–alkali stress at a 0–15 cm soil depth. Increased and decreased surface soil moisture and density of soil bulk were achieved by the second year, respectively, through the application of straw and biochar. These soil amendments also significantly decreased soil electrical conductivity and pH, and the application of biochar significantly reduced the sodium adsorption ratio (SAR refers to the adsorption ratio of sodium ions to other ions in soil) and Na⁺ by 32.1% and 34.7%, respectively, compared with drip irrigation alone. Application of desulfurized gypsum combined with drip irrigation decreased soil pH, SAR, and Na⁺ by 0.25, 41.6%, and 38.1%, respectively, compared with drip irrigation alone. The three soil amendments significantly increased sunflower yields by 51.2–80.0% in the second year, with the biochar treatment showing the most significant impact. The results showed that combined biochar and drip irrigation could play an important role in ameliorating soil salinization in the Hetao Irrigation Area, thereby contributing to increased crop yields and sustainable agriculture. However, given the relatively short experimental duration and the single location of this study, as well as the lack of long-term monitoring of salt balance and drainage conditions, further research with extended timelines, expanded geographic coverage, and focused assessment of salt dynamics is needed to confirm and generalize these findings. Full article

To address the problem of excessive sulfur in high-sulfur magnetite concentrates when used directly, this study systematically investigated the desulfurization behavior and mechanism during oxidative roasting. Green pellets were prepared by mixing high-sulfur iron concentrate fines with 1% bentonite, followed by roasting experiments in air at 800–1200 °C. Thermogravimetric analysis (TG), real-time flue gas analysis (DOAS), X-ray diffraction (XRD), and scanning electron microscopy–energy dispersive spectroscopy (SEM–EDS) were employed to characterize the process and products. The results show that sulfur release is mainly concentrated in two stages: intensive oxidative decomposition of FeS/FeS₂ in the range of 480–580 °C and release of reacted sulfur originally encapsulated within the pellets in the range of 940–1080 °C. It was found that alkali metal oxides CaO and MgO in the feed can fix sulfur at a high temperature. They react with released SO₂ and iron oxides to form Ca/Mg sulfate–iron oxide composite phases, such as (Ca_0.75Mg_0.25)SO₄·0.38Fe₂O₃ and (Ca_0.91Mg_0.09)SO₄·3.66Fe₂O₃·1.47MgO, which slow the SO₂ emission rate. A desulfurization ratio above 99% can be achieved when roasting at 1100 °C and above. This study clarifies the sulfur migration mechanism during the roasting of high-sulfur iron concentrate pellets, providing a theoretical basis for optimizing the roasting process to achieve efficient desulfurization and recovery of iron resources. Full article

The large-scale dredging activities in port areas generate substantial quantities of dredged soil, leading to land occupation and disposal challenges, while industrial wastes such as fly ash and desulfurization gypsum remain underutilized. In this study, industrial wastes were employed as a curing agent to stabilize dredged soil, aiming to achieve both mechanical performance improvement and cost-effective recycling. In total, 100 g of curing agent was added to 1 kg of sludge. The optimal strength-maximizing formulation comprised 4.5% activator 1 #, 4.5% fly ash, 4.5% mineral powder, and 0.5% desulfurization gypsum. It achieved an unconfined compressive strength of 0.794 MPa. For enhanced cost-effectiveness, a modified binder blend (1.88% activator 1 #, 4.5% fly ash, 4.5% mineral powder, and 0.5% desulfurization gypsum) delivered 0.63 MPa at 28 days, satisfying mechanical construction specifications. Results demonstrate that unconfined compressive strength increases with solid wastes; however, with the extension of solidification time, the unconfined compressive strength of dredged soil gradually slows down. Full article

The rational utilization of industrial solid waste is an effective way to reduce environmental pollution. This study investigated the potential application of fluorogypsum (FG), flue gas desulfurization gypsum (FGD), phosphogypsum (PG), and titanium gypsum (TG) in the production of excess-sulfated slag cement (ESSC). It further investigated the effects of different types of gypsum on the performance and hydration process of ESSC through a wet grinding process. The results showed that as the pH value of the gypsum increased, the setting time of ESSC decreased, and hydration heat release occurred earlier. Phase analysis and microstructural characterization indicated that the type of gypsum affected the hydration rate, microstructure, and quantity of hydration products of ESSC, thereby influencing its compressive strength. To further improve the performance of ESSC, a wet grinding process was employed to enhance particle activity and promote hydration reactions. PG, due to its high solubility, demonstrated a better activation effect; after wet grinding, the 28 d compressive strength reached 40.03 MPa. Meanwhile, ESSC pastes prepared with high-pH FG exhibited not only good early strength (3-day strength of 21.93 MPa) after wet grinding but also excellent water resistance, with a softening coefficient of 0.96. This study clarifies the impact of gypsum type on ESSC performance and provides valuable insights for enhancing its properties. Full article

To enhance the rheological properties and engineering applicability of fully solid waste filling slurry, this study uses iron tailings sand as aggregate and slag, steel slag, and desulfurization ash as cementing materials. Through a central composite design experiment, the synergistic regulatory effects of steel slag (10~30%) and desulfurization ash (10~30%) on the slurry’s rheological and strength properties were systematically investigated. The yield stress and plastic viscosity of the slurry were quantified based on the Bingham fluid model, using expansion tests and L-tube models, while isothermal calorimetry analysis and microscopic image processing revealed the underlying micro-mechanisms. The results show that when both steel slag and desulfurization ash contents are 20%, the cured specimen prepared from the slurry achieves an optimal 28-day uniaxial compressive strength of 5.90 MPa at 28 days, with yield stress and plastic viscosity of 146.71 Pa and 3.04 Pa·s, respectively. Micro-mechanistic analysis revealed that desulfurization ash effectively reduced the yield stress by up to 38% (from 196.04 Pa to 90.01 Pa) and increased the fractal dimension of flocculated structures to 1.906, thereby optimizing initial flowability. Conversely, steel slag increased the yield stress but decreased plastic viscosity, enhancing structural stability, and regulating the later hydration process. The loop tests confirmed the good transport performance and engineering adaptability of the optimized mix, achieving a cost reduction of up to 65% compared to cement-based systems. Full article

This study aimed to develop sustainable supersulfated cement (SSC) comprising ferronickel slag (FNS), desulfurized gypsum, carbide slag, and a small amount of Portland cement (PC). A two-stage optimization approach considering mechanical strength, volume stability, durability, and sustainability was employed to screen the mixture proportions of low-clinker FNS-based SSC. Orthogonal experiments were firstly conducted to investigate the effects of PC, carbide slag, and desulfurized gypsum contents on the mechanical properties of SSC mortar. Range analysis revealed that carbide slag exerted the most significant impact on early-age mechanical strength, while desulfurized gypsum plays an increasingly important role in late-age strength development. Subsequently, a single-factor test was applied to determine the optimal carbide slag content in FNS-based SSC. The results demonstrated that with the incorporation of 4% carbide slag, the SSC mortar achieved the 3-day and 28-day compressive strengths of 15.88 and 42.5 MPa, with relatively low volumetric expansion. The screened mixture proportions also satisfied the requirements for strength class 42.5 SSC according to both Chinese and British standards. A life cycle assessment further indicated that its carbon emission was approximately 46.91% lower than that of conventional PC. This research provided key technical and data support for the synergistic utilization of multi-source solid wastes in producing low-carbon cementless binder. Full article

The low activity and expansion risk of steel slag limit its large-scale utilization in cementitious systems. This study developed an alkali-sulfate synergistic activation method to prepare binder with steel slag content exceeding 50 wt%. The effects of alkali activator dosage, modulus, steel slag and flue gas desulfurization gypsum content on the mechanical properties and workability were systematically investigated. With a mix of 60% steel slag, 30% fly ash, 10% desulfurization gypsum and activated by additional 20% alkali activator with modulus 1.0, the 28-day compressive strength reached 12.85 MPa, along with excellent volume stability. Microstructural characterization revealed that the main hydration products are C-A-S-H and ettringite, which jointly form a dense microstructure. When used to solidify lead–zinc tailings for backfill, the binder yielded satisfactory strength and effectively immobilized heavy metals (Pb, As, Cd, Zn), with leaching concentrations meeting environmental standards and immobilization efficiencies > 80%. Heavy metals were primarily immobilized through physical encapsulation, ion exchange, and co-precipitation. This study elucidates the hydration and mechanisms of high-content steel slag systems under alkali-sulfate synergistic activation, providing a sustainable technical framework for large-scale utilization of steel slag and tailings management. Full article

Hydrogen sulfide (H₂S) commonly exists in natural gas, syngas, and coal-derived gas, and the elimination of H₂S from industrial gases is essential before application. In this study, we utilized low-cost lignite as a raw material. After acid-washing pretreatment, nitrogen-containing substances (urea or dicyandiamide) were incorporated into the coal, and two types of N-modified activated carbon desulfurizers for ambient-temperature H₂S removal were prepared via an in situ loading method, integrating the synthesis of activated carbon with the loading of active components. When the dicyandiamide content was 9 wt.%, and the oxygen concentration for desulfurization was 5%, the breakthrough time reached 550 min with a corresponding breakthrough sulfur capacity of 79.6 mg/g. Characterization revealed that the dicyandiamide-N-modified desulfurizer possessed elevated oxygen and nitrogen contents, which may partially augment the density of surface alkaline active sites. This enhancement is likely to induce alkalization of the interfacial water layer, thereby potentially accelerating H₂S dissociation into HS⁻ and subsequently facilitating its oxidative conversion to elemental sulfur via reaction with oxygen. Full article

In this study, CaO-SiO₂-Al₂O₃-MgO-TiO₂ slag was used as the research object to simulate the blast furnace ironmaking process. Based on the experimental data, the influences of basicity (R(w(CaO)/w(SiO₂))) and the magnesia–alumina ratio (w(MgO)/w(Al₂O₃)) on desulfurization ability are discussed. Additionally, the influences of dissimilarity, basicity, and the magnesia–alumina ratio on slag structure were analyzed using Fourier transform infrared spectroscopy (FT-IR). The results show that when w(Al₂O₃) = 20% and w(MgO)/w(Al₂O₃) = 0.50, sulfide capacity (lgC_s) accretion with the increment in R. Moreover, when w(Al₂O₃) = 20% and R = 1.30, sulfide capacity accretion with the increment in w(MgO)/w(Al₂O₃). Fourier transform infrared spectroscopy was used to confirm that, with increasing basicity and the magnesia–alumina ratio, the concentration of dissociated free oxygen ions (O²⁻) in slag increases, and these ions interact with the bridging oxygen (O⁰) of silicate to depolymerize the complex Si-O structure into simpler units. Full article