Search Results (35)

In the race for industrialization and urbanization, the concentration of greenhouse gases like CO₂ and CH₄ is growing rapidly and ultimately resulting in global warming. An Ni-based catalyst over MgO support (Ni/MgO) offers a catalytic method for the conversion of these gases into hydrogen and carbon monoxide through the dry reforming of methane (DRM) reaction. In the current research work, 1–4 wt% strontium is investigated as a cheap promoter over a 5Ni/MgO catalyst to modify the reducibility and basicity for the goal of excelling the H₂ yield and H₂/CO ratio through the DRM reaction. The fine catalytic activities’ correlations with characterization results (like X-ray diffraction, surface area porosity, photoelectron–Raman–infrared spectroscopy, and temperature-programmed reduction/desorption (TPR/TPD)) are established. The 5Ni/MgO catalyst with a 3 wt.% Sr loading attained the highest concentration of stable active sites and the maximum population of very strong basic sites. 5Ni3Sr/MgO surpassed 53% H₂ yield (H₂/CO ~0.8) at 700 °C and 85% H₂ yield (H₂/CO ratio ~0.9) at 800 °C. These outcomes demonstrate the catalyst’s effectiveness and affordability. Higher Sr loading (>3 wt%) resulted in a weaker metal–support contact, the production of free NiO, and a lower level of catalytic activity for the DRM reaction. The practical and cheap 5Ni3Sr/MgO catalyst is scalable in industries to achieve hydrogen energy goals while mitigating greenhouse gas concentrations. Full article

Petroleum is an indispensable energy source in modern industrial society, and maintaining the safe and stable operation of its injection and production system is of great significance. To analyze the mechanism of pipeline damage caused by corrosion and scaling in the injection production system, taking a water injection pipeline in an oil field as an example, the causes of corrosion and scaling damage were studied by detecting pipeline samples and analyzing corrosion products and various service conditions of the pipeline. The results showed that there was more scaling on the inner wall of the pipeline, and there was local corrosion in the pipeline sections that had experienced water injection, shutdown, and gas injection conditions, while there was no significant corrosion thinning in the pipeline sections that had only experienced water injection and shutdown conditions. The scale layer formed under water injection conditions is mainly composed of barium strontium sulfate (Ba_0.75Sr_0.25SO₄), barium sulfate (BaSO₄) and a small amount of silica (SiO₂). The main reason for scale formation is the high content of barium ions (Ba²⁺) in the injected water. The corrosion products formed under gas injection conditions, including strontium ions (Sr²⁺) and sulfate ions (SO₄²⁻), are mainly composed of ferrous carbonate (FeCO₃) and ferric oxide (Fe₂O₃). The pipeline corrosion product FeCO₃ is mainly caused by carbon dioxide (CO₂) in the medium. In addition, the high liquid content, cecal position, high Cl⁻ (chloride ion) content, and slightly acidic environment in the pipeline also accelerate the occurrence of corrosion damage. The Fe₂O₃ in the corrosion products is formed when the pipeline is exposed to air after sampling, and is not the main cause of pipeline corrosion. Full article

Achieving net-zero carbon emissions, this study introduces a sustainable pathway for reducing strontium sulfate (SrSO₄) and celestite ore to strontium sulfide (SrS) using biofuels (biomethane, bioethanol) derived from agro-industrial waste and green hydrogen. Traditional SrSO₄ reduction methods, which rely on fossil-derived reductants like coal and operate at energy-intensive temperatures (1100–1200 °C), generate significant greenhouse gases and toxic byproducts, highlighting the need for eco-friendly alternatives. Experimental results demonstrate that bioethanol outperformed other reductants, achieving 97% conversion of synthetic SrSO₄ at 950 °C within 24 min and 74% conversion of natural celestite ore over 6 h. Remarkably, this bioethanol-driven process matches the energy efficiency of the conventional black ash method while enabling carbon neutrality through renewable feedstock utilization, reducing CO₂ emissions by 30–50%. By valorizing agro-industrial waste streams, this strategy advances circular economy principles and aligns with Mexico’s national agenda for sustainable industrial practices, including its commitment to decarbonizing heavy industries. This study contributes to sustainable development goals and offers a scalable solution for decarbonizing strontium compound production in the chemical industry. Full article

Crystal violet dye poses significant environmental and human health risks due to its toxicity, persistence, and bioaccumulative nature. It contributes to potential carcinogenicity, cytotoxicity, and systemic toxicity upon human exposure. To address this issue, a novel SrCO₃/MgO/CaO/CaCO₃ nanocomposite was synthesized using the Pechini sol-gel method, producing AE500 and AE700 at 500 and 700 °C, respectively, for the efficient removal of crystal violet dye from aqueous media. X-ray diffraction (XRD) analysis confirmed the formation of crystalline phases, with average crystallite sizes of 64.53 nm for AE500 and 75.34 nm for AE700. Energy-dispersive X-ray spectroscopy (EDX) revealed elemental compositions with variations in carbon, oxygen, magnesium, calcium, and strontium percentages influenced by synthesis temperature. Field-emission scanning electron microscopy (FE-SEM) showed morphological differences, where AE500 had irregular polyhedral structures, while AE700 exhibited more compact spherical formations, with average grain sizes of 99.98 and 132.23 nm, respectively. High-resolution transmission electron microscopy (HR-TEM) confirmed the structural integrity and nano-scale morphology, showing aggregated irregularly shaped particles in AE500, while AE700 displayed well-defined polyhedral and nearly spherical nanoparticles. The calculated average particle diameters were 21.67 nm for AE500 and 41.19 nm for AE700, demonstrating an increase in particle size with temperature. Adsorption studies demonstrated maximum capacities of 230.41 mg/g for AE500 and 189.39 mg/g for AE700. The adsorption process was exothermic, spontaneous, and physical, following the pseudo-first-order kinetic model and Langmuir isotherm, indicating monolayer adsorption onto a homogenous surface. Full article

This study analyzes the mineralogical and geochemical composition of 38 surface sediment samples from the northwest African continental shelf between Cap Boujdour (26.5° N) and Cap Blanc (20.5° N). Using a multiproxy approach, sediment characteristics were assessed through grain size, calcium carbonate (CaCO₃), and organic carbon (Corg) measurements, along with X-ray diffraction (XRD) and X-ray fluorescence (XRF) for geochemical analysis. Bottom water properties, including temperature, salinity, and dissolved oxygen, were measured at various stations using a Conductivity, Temperature, and Depth (CTD) sensor. The results reveal that the inner shelf sediments are primarily mud, with high concentrations of terrigenous elements such as iron (Fe), silicon (Si), rubidium (Rb), and potassium (K), with Fe and Si concentrations ranging from 2.1 to 4.3 wt%. The middle and outer shelf sediments are dominated by biogenic carbonates, with CaCO₃ levels approaching 65%, and elevated calcium (Ca) and strontium (Sr) content. These areas also exhibit the highest bottom water temperatures (up to 16 °C), salinity (36%), and moderate oxygen levels (2–4 mL/L). Slope sediments are enriched with mud and montmorillonite, and aeolian contributions are more pronounced south of Dakhla, as indicated by elevated quartz levels (up to 20%) and the presence of illite, aluminum oxide (Al₂O₃), and iron oxide (Fe₂O₃). This study provides valuable new insights into sedimentary processes on the northwest African shelf, offering implications for regional environmental management and resource exploration. Full article

The chemical looping reforming of methane using an SrFeO₃ oxygen carrier to produce synthesis gas from solar energy was experimentally investigated and validated. High-temperature solar heat was used to provide the reaction enthalpy, and therefore the methane feedstock was entirely dedicated to producing syngas. The two-step isothermal process encompassed partial perovskite reduction with methane (partial oxidation of CH₄) and exothermic oxidation of SrFeO_3-δ with CO₂ or H₂O splitting under the same operating temperature. The oxygen carrier material was shaped in the form of a reticulated porous foam structure for enhancing heat and mass transfer, and it was cycled in a solar-heated tubular reactor under different operating parameters (temperature: 950–1050 °C, methane mole fraction: 5–30%, and type of oxidant gas: H₂O vs. CO₂). This study aimed to assess the fuel production capacity of the two-step process and to demonstrate the potential of using strontium ferrite perovskite during solar cycling for the first time. The maximum H₂ and CO production rates during CH₄-induced reduction were 70 and 25 mL/min at 1000 °C and 15% CH₄ mole fraction. The increase in both the cycle temperature and the methane mole fraction promoted the reduction step, thereby enhancing syngas yields up to 569 mL/g during reduction at 1000 °C under 30% CH₄ (778 mL/g including both cycle steps), and thus outperforming the performance of the benchmark ceria material. In contrast, the oxidation step was not significantly affected by the experimental conditions and the material’s redox performance was weakly dependent on the nature of the oxidizing gas. The syngas yield remained above 200 mL/g during the oxidation step either with H₂O or CO₂. Twelve successive redox cycles with stable patterns in the syngas production yields validated material stability. Combining concentrated solar energy and chemical looping reforming was shown to be a promising and sustainable pathway toward carbon-neutral solar fuels. Full article

The greenhouse gas CH₄ is more potent than CO_2, although both these gases are solely responsible for global warming. The efficient catalytic conversion of CH₄ into hydrogen-rich syngas, which also demonstrates economic viability, can deplete the concentration of CH₄. This study examines the partial oxidation of methane (POM) prepared by the wetness impregnation process using 5% Ni supported over DSZ95 (93.3% ZrO₂ + 6.7% Sc₂O₃) and promoted with 1% Ga (gallium), 1% Sr (strontium), and 1% Ce (cerium). These catalysts are characterized by surface area porosity, X-ray diffraction, FT-Infrared spectroscopy, Raman infrared spectroscopy, temperature programmed reduction, CO₂ temperature-programmed techniques, desorption techniques, thermogravimetry, and transmission electron microscopy. The characterization results demonstrate that Ni is appropriate for the POM because of its crystalline structure, improved metal support contact, and increased thermal stability with Sr, Ce, and Ga promoters. The synthesized catalyst 5Ni+1Ga-DSZ95 maintained stability for 240 min on stream during the POM at 700 °C. Adding a 1% Ga promoter and active metal Ni to the DSZ95 improved the CH₄ conversion from 70.00% to 75.90% and raised the H₂ yield from 69.21% to 74.80%, while maintaining the reactants’ stoichiometric ratio of (CH₄:O₂ = 2:1). The 5Ni+1Ga-DSZ95 catalyst is superior to the other catalysts, given its rich catalyst surface, strong metal support interaction, high surface area and low amount of carbon deposit. The high H₂/CO ratio (>2.6) and H₂ yield close to 75% indicate that 5Ni+1Ga-DSZ95 is a potent industrial catalyst for hydrogen-rich syngas production through partial oxidation of methane. Full article

The Kraaipan and Amalia greenstone belts in South Africa occur in the western part of the Kaapvaal Craton. The two belts stretch discontinuously in an approximately north–south orientation over a distance of about 250 km from southern Botswana in the north to the Vaal River near Christiana in the south and are separated by a distance of about 90 km. Gold mineralization is hosted in banded iron formation at both the Kalahari Goldridge deposit (Kalgold) in the Kraaipan greenstone belt in the north and the Amalia deposit in the Amalia greenstone belt in the south, with the mineralization associated with quartz–carbonate veins. The footwalls of these deposits are generally composed of mafic volcanic schist and the hanging walls consisting of graywackes, schist and shale units. The Kalgold and Amalia gold deposits show some variation in the redox condition of the mineralizing system and fluid chemistry. The ore mineral assemblage is characterized by magnetite–pyrrhotite–pyrite at Kalgold, which is indicative of reducing conditions, and a magnetite–hematite–pyrite assemblage at Amalia that suggests a relatively oxidizing environment. Average mineralizing temperatures determined from chlorite geothermometry were relatively higher at the Kalahari Goldridge deposit ranging from 350 to 400 °C compared to the slightly cooler range of 330 to 390 °C at Amalia. The composition of the fluids derived from fluid inclusions is indicative of low salinity H₂O--CO₂±CH₄-rich fluids at Kalgold against relatively H₂O-CO₂-rich fluids at Amalia. Evidence from strontium–carbon–oxygen isotopic ratios from carbonates suggests that differences in redox conditions in the deposits could be attributed to different flow pathways by an evolving fluid from a common source (with minimum ⁸⁷Sr/⁸⁶Sr = 0.70354) to the sites of gold deposition, with a significant ore fluid interaction with a thick sequence of carbonaceous meta-pelitic rock units at the Kalahari Goldridge deposit that is absent in the Amalia deposit. Full article

The objective of this study is to perform a comparative analysis of the impact of incorporating alkaline earth metal carbonates (MCO₃, where M–Mg, Ca, Sr, Ba) into low-calcium fly ash (FA) on the geopolymerization processes and the resultant properties of composite geopolymers. Mechanical activation was employed to enhance the reactivity of the mixtures. The reactivity of the mechanically activated (FA + alkaline earth carbonate) blends towards NaOH solution was experimentally studied using XRD analysis and FTIR spectroscopy. In agreement with thermodynamic calculations, MgCO₃ demonstrated the most active interaction with the alkaline solution, whereas strontium and barium carbonates exhibited little to no chemical interaction, and calcite was situated in the transition region. As the calcite content in the mixture with FA increased, the compressive strength of the geopolymers continuously improved. The addition of Mg, Sr, and Ba carbonates to the FA did not enhance the strength of geopolymers. However, the strength of geopolymers based on these blends was comparable with that of geopolymers based on 100% FA. The strength of geopolymers synthesized from the 100% FA and from the (90% FA + 10% MCO₃) blends, mechanically activated for 180 s, at the age of 180 days was 11.0 MPa (0% carbonate), 11.1 MPa (10% MgCO₃), 36.5 MPa (10% CaCO₃), 13.6 MPa (10% SrCO₃), and 12.4 MPa (10% BaCO₃) MPa, respectively. The influence of carbonate additives on the properties of the composite geopolymers was examined, highlighting filler, dilution, and chemical effects. The latter determined the unique position of calcite among the carbonates of alkaline earth metals. Full article

In this study, geopolymers based on mechanically activated mixtures of fly ash (FA) with SrCO₃ (strontianite) and BaCO₃ (witherite) were synthesized. NaOH solution was used as an alkaline agent and curing was carried out under ambient conditions. XRD, FTIR spectroscopy, thermogravimetry, and SEM were used to study the geopolymerization process and microstructure. The product of geopolymerization of the milled (FA + SrCO₃) and (FA + BaCO₃) blends was X-ray amorphous N-A-S-H gel. The beneficial impact of mechanical activation on the compressive strength of geopolymers was most evident during the initial stages of the curing process. The strength of geopolymers based on the (FA + carbonate) blends after 7 d was either less than the corresponding strength of geopolymers based on the 100% FA or, within the measurement accuracy, equal to it. With increasing curing time, the strength development of geopolymers synthesized from (70% FA + 30% carbonate) blends exceeded the strength growth of geopolymers containing less carbonates; after curing for 180 d, these geopolymers showed the highest compressive strength (20–27 MPa). This trend was more pronounced for the geopolymers based on the (FA + SrCO₃) blends. The influence of SrCO₃ and BaCO₃ addition to the FA on the strength of composite geopolymers was explained by dilution and microfiller effects. The geopolymers based on the FA blended with SrCO₃ and BaCO₃ exhibit potential applications in immobilizing radioactive strontium and producing radiation shielding materials. Full article

The effect of strontium substitution in the structure of the complex oxide Gd₂SrFe₂O₇ on the production of light olefins by CO hydrogenation was investigated. Perovskite-type oxides Gd_2−xSr_1+xFe₂O₇ (x = 0; 0.1; 0.2; 0.3; 0.4) were synthesized by sol–gel technology and characterized by XRD, Mössbauer spectroscopy, BET specific area, acidity testing, and SEM. The experimental data revealed a correlation between the state of iron atoms, acidity, and catalytic performance. It was found that with an increase in the content of Sr²⁺ in the perovskite phase, the basicity of the surface and the oxygen diffusion rate increased. This contributed to the CO dissociative adsorption, formation of active carbon, and its further interaction with atomic hydrogen. Full article

The development of efficient heterogeneous persulfate activators is one of the main research topics in the wastewater treatment area. The present work deals with the heterogeneous activation of sodium persulfate (SPS) using nickel oxide/strontium carbonate (NiO/SrCO₃) for the degradation of sulfamethoxazole (SMX), a representative compound from the group of antibiotics. Results showed that NiO/SrCO₃ exhibited high performance towards the activation of SPS, leading to SMX elimination in brief time spans. The impact of SPS (25–100 mg/L), NiO/SrCO₃ (50–250 mg/L), and SMX (0.25–3.00 mg/L) concentration, and initial pH on the decomposition of SMX was further examined. Experiments were also conducted in real matrices such as secondary effluent and bottled water, revealing the existence of retarding phenomena compared to ultrapure water. This behavior was further investigated with the addition of bicarbonates, chlorides, or humic acid in ultrapure water. It was found that organic matter significantly hampered SMX removal. The role of the main radicals (hydroxyl and sulfate radicals) was determined using appropriate radical traps (methanol and tert-butanol). These quenching experiments combined with the conducted electrochemical measurements revealed that both a radical and a non-radical mechanism contribute to the decomposition of SMX. Full article

In this study, activated carbons derived from walnut shells (CA-N) and apple wood (CA-M) were used as adsorbents to remove cobalt(II) and strontium(II) ions from aqueous solutions. The novel materials were obtained using nitric acid (CA-Mox) and nitric acid/urea mixture (CA-Mox-u, CA-Nox-u) as oxidizing agents. The physical–chemical characteristics of activated carbons were determined from nitrogen sorption isotherms, SEM-EDX, FTIR, pH metric titrations, the Boehm titration method and elemental analysis. The results of batch experiments indicate that maximum adsorption can be achieved in broad pH ranges: 4–8 for Co(II) and 4–10 for Sr(II). The maximum adsorption capacities of Co(II) and Sr(II) on oxidized activated carbons at pH = 4 are: CA-Mox, 0.085 and 0.076 mmol/g; CA-Mox-u, 0.056 and 0.041 mmol/g; and CA-Nox-u, 0.041 and 0.034 mmol/g, respectively. The mathematical models (pseudo-first-order, pseudo-second-order and intraparticle diffusion kinetic models, and Langmuir, Freundlich, Dubinin–Radushkevich, and Temkin–Pyzhev isotherm models) were used to explain the adsorption kinetics, to study the adsorption mechanism and predict maximum adsorption capacity of the adsorbents. The adsorption mechanisms of toxic metal ions on activated carbons were proposed. Full article

This study presents a comprehensive analysis of sediment texture along with geochemical variation, potential sources, and ecological risk assessment of major elements and trace metals in the bottom sediments of Iranian territorial waters situated in the northeast Persian Gulf. To achieve this, diverse laboratory methods, GIS techniques, statistical analyses, and index analysis approaches were employed. Over 50% of the sediment particles are mud, while one-third are sand-sized particles, primarily composed of skeletal fragments. The sediment’s elements concentrations were ranked in descending order as Ca > Al > Fe > Sr > Mn > Ba > Cr > Ni > V > Zn > Cu > Pb > As > Co > Mo > Cd. Cluster analysis revealed strong correlations among Al-Ni-Cr-V, Cd-Cu-Zn-Pb, Ba-Fe, silt-clay, and Ca-Sr. Calcium and strontium showed extremely severe enrichment due to high content of carbonate matter. Arsenic and Mo were significantly enriched, while Ba, V, Co, Zn, and Cu demonstrated moderate enrichment. Nevertheless, all the sampling stations were classified as having zero to very low levels of contamination, indicating a low potential ecological risk. Arsenic emerged as the primary contributor to the ecological risk index. Notably, no strong correlation was found between As, Mo, and other elements, indicating that As and Mo likely originate from distinct sources. Full article

Solar-driven evaporation technology is often used in areas with limited access to clean water, as it provides a low-cost and sustainable method of water purification. Avoiding salt accumulation is still a substantial challenge for continuous desalination. Here, an efficient solar-driven water harvester that consists of strontium-cobaltite-based perovskite (SrCoO₃) anchored on nickel foam (SrCoO₃@NF) is reported. Synced waterways and thermal insulation are provided by a superhydrophilic polyurethane substrate combined with a photothermal layer. The structural photothermal properties of SrCoO₃ perovskite have been extensively investigated through state-of-the-art experimental investigations. Multiple incident rays are induced inside the diffuse surface, permitting wideband solar absorption (91%) and heat localization (42.01 °C @ 1 sun). Under 1 kW m⁻² solar intensity, the integrated SrCoO₃@NF solar evaporator has an outstanding evaporation rate (1.45 kg/m² h) and solar-to-vapor conversion efficiency (86.45% excluding heat losses). In addition, long-term evaporation measurements demonstrate small variance under sea water, illustrating the system’s working capacity for salt rejection (1.3 g NaCl/210 min), which is excellent for an efficient solar-driven evaporation application compared to other carbon-based solar evaporators. According to the findings of this research, this system offers significant potential for producing fresh water devoid of salt accumulation for use in industrial applications. Full article