Search Results (729)

Due to the low hydration activity of steel slag, its mechanical properties are insufficient, which limits its strategic application in steel slag based cementitious composite. In this study, the promoting effect of calcined layered double hydroxide (CLDH) on the hydration process, mechanical properties, and microstructure of high-volume steel slag cementitious materials was systematically investigated. The results showed that the addition of CLDH significantly optimized the material’s performance. When the mass fraction of steel slag was 70 wt% and the CLDH dosage was 2.0 wt%, the 7-day compressive strength reached 42.5 MPa, indicating an increase of 23.9% compared with the control group. Microscopic characterization suggested that CLDH slightly enhanced the hydration reaction of steel slag and increased the generation of hydration products through the nucleation effect. The addition of CLDH demonstrated a change in the composition of C-(A)-S-H to a higher Al/Ca ratio. Meanwhile, the lamellar structure of CLDH effectively filled the pores and promoted the densification of the matrix. This research provides valuable insights for the high-value utilization of steel slag and the design of high-performance cementitious materials. Full article

Magnetic nanoparticles represent the next-generation drug delivery systems, enabling drug targeting to specific organs without adverse effects on the body and with a controlled release rate. Their strengths are represented by biocompatibility, low cost, and easy drug loading; some drawbacks are aggregation and poor stability in biological media. In the present work, we synthesized magnetic core–shell structures with a magnetite core coated with layered double hydroxides (LDHs) based on Mg²⁺ or Zn²⁺ and Al³⁺ ions and loaded with meloxicam, a poorly water-soluble anti-inflammatory drug. Several syntheses have been attempted to obtain iron oxides based on the only magnetite phase. The combined use of different characterization techniques allowed us to reveal that the best product, showing the crucial room temperature superparamagnetism and a good level of compositional uniformity, was obtained from co-precipitation in nitrogen flow. The next LDH coating was successful, even if the hybrids showed the occurrence of aggregation. The drug was mainly adsorbed onto the LDH surfaces, as shown by the X-ray diffraction and Infrared Spectroscopy techniques. The loaded meloxicam amount was low, but the subsequent release into simulated body fluid could be prolonged for 4 days. Our study provides a proof of concept about the importance of a thorough characterization of the nanocomposite hybrids and their possible use for tricky drugs, such as those of class II of the Biopharmaceutical Classification System. Full article

ZnMgAl layered double hydroxides (LDHs) were synthesised via coprecipitation, and oleic acid and stearic acid were grafted onto their surfaces via dehydration condensation to obtain two nano-lubricant additives, OA-ZnMgAl LDH and SA-ZnMgAl LDH. These surface modifications significantly improved the dispersion stability of ZnMgAl LDH in lubricating oil. Tribological tests showed that, at their respective optimal concentrations for friction reduction or wear resistance, ZnMgAl LDH, OA-ZnMgAl LDH, and SA-ZnMgAl LDH reduced the coefficient of friction by 3%, 20%, and 16%, and decreased the wear scar diameter by 7%, 9%, and 14%, respectively, compared with the base oil (XMP-Mobil 320). To clarify the lubrication mechanism, the wear morphology and chemical composition were analysed using 3D optical profilometry, X-ray photoelectron spectroscopy, scanning electron microscopy, and FIB-SEM. The results indicate that LDHs react with the steel surface under load and shear to form a multilayer protective film consisting of an inner oxide layer and an outer graphite layer, preventing direct contact between friction pairs. In addition, the rolling and filling effects of partially unreacted LDHs further reduce friction and wear. Full article

This study investigated a feasible recycling and detoxification process for waste tire ash containing hazardous Zn and Al using acid leaching, followed by layered double hydroxide (LDH) synthesis. The novelty of this work is the direct conversion of a Zn/Al/Fe/Ca-rich real waste system into a phosphorus removal material, in which LDH-related uptake and secondary hydroxyapatite formation cooperatively immobilize phosphorus. Waste tire ash mainly consists of Zn, Al, Fe, Ca, and Si, most of which can be effectively leached with hydrochloric acid (HCl). The optimum leaching conditions for high extraction efficiency involved treatment with 10 M HCl for 10 min at 20 °C (solid–liquid ratio: 50 g/L). Under these conditions, the elution concentrations of Zn and Al from the residue decreased to 0.3 and 0.17 mg/L, respectively, meeting the Japanese leaching standards, whereas the raw ash showed significantly higher values. From the leached solution, LDH-containing products with high phosphorus removal capacity were synthesized at 40 °C for 2 h by adjusting the pH to 11.5. A phosphorus removal performance of 2.0 mmol/g was obtained owing to the formation of hydroxyapatite. The combined process of HCl leaching and LDH synthesis enables the detoxification of waste tire ash and the production of an environmental purification material. Full article

Earthen immovable cultural relics, such as murals and painted clay sculptures, are prone to deterioration (e.g., efflorescence, flaking, and cracking) under long-term preservation conditions. While conventional restoration materials primarily offer reinforcement, they fail to regulate the migration of soluble salts within the relics, which is the main cause of such damage. Herein, aimed at protecting the painted sculptures and murals of the Yungang Grottoes, nano calcium-aluminum layered double hydroxides (Ca-Al LDHs) were prepared, and their effectiveness in regulating salt crystallization within the earthen ground layer, as well as their reinforcement performance were investigated. Simulated salt crystallization tests revealed that coating the ground layer with Ca-Al LDHs delayed salt-induced damage time by 150%. This can be attributed to the ability of Ca-Al LDHs to adsorb sulfate ions from soluble salts, thereby inhibiting the crystallization of magnesium sulfate on the surface of the ground layer. After curing Ca-Al LDHs-coated samples at 35 °C and 55% relative humidity (RH) for 7 days, their surface Leeb hardness increased by 3.1%, and the weight loss rate (measured via tape peeling test) decreased by 38.3%. These results indicate that the surface bonding strength was enhanced following Ca-Al LDHs coating, with the underlying mechanism being the transformation of part of the LDHs into calcium carbonate under the influence of water and carbon dioxide. This study demonstrates that Ca-Al LDHs not only suppress magnesium sulfate crystallization but also provide effective surface consolidation, showing promising potential for application in conserving painted sculptures and murals at the Yungang Grottoes. Full article

This study investigates the gel characteristics of alkali-activated materials (AAMs) synthesized using wood ash (WA), and metakaolin (MK) as solid precursors. The research explores the influence of precursor type and sodium hydroxide (NaOH) concentrations in the alkali activator solution on the resulting physicochemical, microstructural, mechanical, and radiological properties of gels. The alkaline activators were prepared by mixing sodium hydroxide solutions (6 M and 12 M) with a sodium silicate (water glass) solution at a volume ratio of 1.5. The physicochemical characteristics of raw materials and AAMs were thoroughly analyzed using X-ray fluorescence (XRF), Diffuse Reflectance Infrared Fourier Transform (DRIFT) spectroscopy, X-ray diffraction (XRD), and scanning electron microscopy (SEM) with EDS elemental mapping. FTIR analysis confirmed the formation of an amorphous gels geopolymer network. XRD revealed the presence of characteristic crystalline phases (quartz, calcite) within an amorphous matrix. Mechanical properties, such as compressive strength, depended on precursor type and alkali molarity: metakaolin (12 M) reached ~14 MPa, while wood ash showed ~4 MPa (6 M) and ~0.5 MPa (12 M) due to high CaO, low Si and Al, and unfavorable SiO₂/Al₂O₃ (5.71) and Na₂O/Al₂O₃ (3.19) ratios. Furthermore, this research estimates radiological doses by quantifying radionuclide content via gamma-spectrometry. Alkali activation significantly reduced radiological hazard parameters, with radium equivalent activity (Ra_eq) decreasing to 238.0 Bq/kg and the external hazard index (H_ex) to 0.643 for A₁₂MK, while the annual effective dose rate for A₁₂WA was only 0.265 nSv/y-all values remaining well below the recommended safety limit of 370 Bq/kg (≤1 mSv/y). The decrease in activity concentration index (I_γ), Ra_eq, and H_ex with increasing NaOH concentration indicates effective radionuclide immobilization within the geopolymer matrix, confirming the suitability of these alkali-activated materials for safe use in construction from a radiation protection perspective. Full article

Colistin sulfate (COL), a critical last-line antibiotic, poses a severe environmental threat due to its persistence and role in spreading mobile resistance genes. This study introduces a novel quaternary Ni-Co-Zn-Al layered double-hydroxide/activated carbon composite (Q-LDH/AC) for highly efficient COL remediation. The composite’s unique architecture, revealed through comprehensive characterization, enables an exceptional adsorption capacity of 952.52 mg·g⁻¹ under optimal conditions (pH 7, 55 °C), a value that significantly surpasses those reported for most previous adsorbents. The process was spontaneous and endothermic, with kinetics and isotherms best described by the pseudo-second-order and Langmuir–Freundlich models, respectively, indicating a complex mechanism dominated by chemisorption on both homogeneous and heterogeneous sites. A key innovative feature is the successful regeneration and reusability of the composite, which retained over 70% efficiency after five cycles, enhancing its potential for practical, cost-effective water treatment applications. The thermodynamic parameters (ΔG° = −8140.68 kJ/mol, ΔH° = +61.22 kJ/mol) indicate that the reaction is spontaneous and endothermic. The interaction mechanism of COL on Q-LDH/AC can be deduced by FT-IR including hydrogen bonding, π-π bonding, electrostatic interactions, and surface complexation. Beyond mere regeneration, this work demonstrates a pioneering circular economy strategy by repurposing the spent COL-laden adsorbent not as waste, but as a high-performance electrocatalyst. In direct urea fuel cell tests, this electrode achieved a superior and stable current density of 45.63 mA/cm² for Q-LDL/AC, substantially outperforming the pristine Q-LDH/AC/COL (206.63 mA/cm²) and highlighting how the captured pollutant enhances functionality. This dual-purpose approach successfully closes the loop, transforming the environmental liability of antibiotic-laden waste into a valuable resource for energy applications. With a production cost of 2.755 USD/g, this work presents not only a highly effective adsorbent but also a transformative, circular strategy that simultaneously addresses water pollution and energy recovery. These findings offer a promising dual-purpose solution for mitigating the environmental spread of antibiotic resistance through a sustainable cycle that enables efficient antibiotic removal from wastewater while simultaneously converting the captured pollutant into a useful energy resource. Full article

This study investigated the antibacterial activities of Se-Al/Zn layered double hydroxide (LDH) and its polycarbazole (PCz) hybrid against Gram-positive Bacillus subtilis and Gram-negative E. coli cells. Antibacterial performances were evaluated using zone of inhibition assays, viable cell counting, and measurement of metabolic activity based on intracellular ATP levels. The collective results showed that both materials exhibited significant antibacterial activity, with PCz–Se–Al/Zn LDH demonstrating enhanced antibacterial activity compared to Se–Al/Zn LDH. Fluorescent live/dead staining and scanning electron microscopy revealed that treatment with either material resulted in loss of metabolic activity and induction of a non-culturable state in bacterial cells, without observable membrane damage or pronounced morphological changes. Possible antibacterial mechanisms of action associated with LDH and PCz–LDH systems are briefly discussed. Full article

Quaternary Ni-Zn-Mg-Al metallic mixed oxide (MMO) catalysts were synthesized by co-precipitation from layered double hydroxide precursors. The effect of varying Zn content on physicochemical properties and catalytic performance was evaluated. Mg-Al and ternary Ni-Mg-Al and Zn-Mg-Al catalysts were synthetized for comparative purposes. XRD, N₂ sorption, MP-AES, CO₂-TPD, NH₃-TPD, SEM, and EDS characterized the materials’ physicochemical properties. The tested reaction was the transesterification between glycerol and dimethyl carbonate to obtain glycerol carbonate to improve the biodiesel industry. The catalyst containing both Ni and Zn showed the highest glycerol conversion among the evaluated materials. This was related to the increased number and strength of surface basic and acid active sites. Specifically, a high density of strong basic sites and acid ones in the quaternary catalysts was required for the reaction mechanism. The catalyst with 20 at% of Zn (MMO-Ni₁₅Zn₂₀) achieved the highest glycerol carbonate yield (89.6%) under mild reaction conditions and was solvent-free. MMO-Ni₁₅Zn₂₀ catalytic performance was associated with its high total basicity and predominance of strong basic sites and a moderate amount of acid sites. The differences observed between catalytic performances suggest that these results depend on the influence of structural, textural, acid, and basic properties. Reuse tests of the MMO-Ni₁₅Zn₂₀ catalyst showed moderate stability, with a progressive decrease in activity due to the loss of strong basic sites and the formation of agglomerated regions. Nevertheless, MMO-Ni₁₅Zn₂₀ maintained a GC selectivity of 100% in the successive cycles. Full article

Effective treatment of coal slime water is essential for sustainable coal preparation plant operation but hindered by the stable suspension of fine, negatively charged particles. To address this, a novel star-shaped inorganic–organic hybrid polymer (aluminum hydroxide-polyacrylamide, Al-PAM) was synthesized via in situ polymerization. Its performance was systematically compared with well-established coagulants/flocculants—polyaluminum chloride (PAC), non-ionic polyacrylamide (NPAM), and their binary combination through settling tests and quartz crystal microbalance with dissipation monitoring (QCM-D). The results showed a positive correlation between the molecular weight of Al-PAM and its flocculation efficiency. The optimal variant, Al-PAM-442, achieved an exceptionally high initial settling rate (50.4 m/h) and low supernatant turbidity (45.77 NTU) at an ultralow dosage of 6 mg/L. QCM-D analysis elucidated the mechanism: Al-PAM forms a thick, soft, and irreversibly adsorbed hydrated layer on silica, enabling strong electrostatic anchoring and effective polymer bridging. In contrast, PAC adsorption was reversible, while NPAM formed a thin, compact film with poor bridging capacity. Although the combined PAC/NPAM system showed synergistic performance, it required a significantly higher dosage (70 mg/L). This study demonstrates that the star-shaped Al-PAM architecture successfully integrates charge neutralization and bridging into a single molecule, offering a highly efficient and practical solution for industrial coal slurry dewatering. Full article

Sugar fatty acid esters represent promising scaffolds for technological applications. These compounds are low-cost and allow rapid modulation of their properties. In this study, we have shown that lipase obtained from solid fermentation from Aspergillus niger (hydrolytic activity of 8.32 × 10⁶ U/g) can promote a selective route towards the 2,5-dissubstituted D-mannitol laurate. Indeed, the lipase hydrolytic activity allowed the yield of 80% in DMF (P.A.) at 55 °C and 6 h. Finally, Mg/Al layered double hydroxides (LDH) were compared towards the selectivity of the expected dissubstituted product. The data obtained through the comparative analysis allows establishing some variables such as solvent (DMF), temperature (55 °C) and solvent dehydration degree for obtaining these molecules for future application studies in supramolecular gelation systems. Full article

This paper presents a focused review of a closed-loop system for sustainable hydrogen production utilizing the reaction between metallic aluminum powders and water, coupled with renewable energy-driven recycling of aluminum hydroxide (or alumina) byproducts back to metallic aluminum powders. A green energy closed-loop system based on aluminum could be achieved if the converting process is accomplished by a green Hall–Héroult process, where a cermet inert anode was used. Meanwhile, the byproduct alumina is converted back to the liquid form of aluminum at high temperature (up to 960 °C), producing pure oxygen. A high-pressure atomization process is then used to break the aluminum droplets into powder using argon gas. The technical feasibility, thermodynamic efficiency, economic viability, environmental sustainability, and comparison of this green aluminum cycle with existing hydrogen production and energy storage technologies are discussed. The aluminum–water reaction offers exceptional energy density (29.7 kJ/g of Al), ambient temperature operation, and zero direct carbon emissions. However, commercial implementation faces substantial challenges including overall round-trip energy efficiency (estimated 34.5–46.6%), technological maturity of the recycling process, passivation layer management, and economic competitiveness with conventional water electrolysis. Despite these challenges, the system demonstrates advantages for seasonal energy storage, off-grid applications, and integration with intermittent renewable energy sources. This analysis provides a framework for researchers, engineers, and policymakers to assess the potential role of aluminum-based energy cycles in the global energy transition toward carbon neutrality. Full article

To mitigate the exhausting of phosphate rock (PR) reserves and the widespread water eutrophication due partially to excessive phosphorus (P), efficient adsorbents are valuable. Calcium (Ca) and aluminum (Al) containing layered double hydroxides (CaAl-LDHs) showed high P adsorption capacity and potential as slow-release P fertilizers, which merits further investigation. Two P proportions (5% and 10%) of P-adsorbed CaAl-LDHs (P-LDHs) were prepared, and its effects on various soil P contents and oilseed rape (Brassica napus L.) growth were evaluated. The main components of 5%P-LDH were P-intercalated CaAl-LDH and brushite, while 10%P-LDH mainly consisted of brushite. The proportions of P were extracted from 10%P-LDH and increased in the order of 4.9% (deionized water) < 48.9% (Olsen method) < 63.5% (Bray method) < 67.4% (citric acid), which suggested that 10%P-LDH could be citrate-soluble P fertilizer. 10%P-LDH showed similar effects on soil available P with single superphosphate (SSP). Both 5%- and 10%P-LDHs showed comparable improvement with SSP on aboveground dry weight of oilseed in the red soil, while being inapparent in the Fluvo-aquic soil. The CaAl-LDH appeared capable of providing Ca for rape growth in the low initial P concentration red soil, which showed the highest dry weight when combined with SSP. The recycled P-LDHs, especially 10%P-LDH, could supply P in a comparable manner with SSP for oilseed rape P uptake. Based on trials conducted under controlled conditions, our study suggested a promising production route of commercial P fertilizer alternatives via water P removal by CaAl-LDH. Further validations with realistic wastewater P removal by CaAl-LDH and via field scale growth trials are still needed before wide application of the alternative P fertilizer production procedure reported in the present study. Full article

The increasing demand for lithium-ion batteries (LIBs) has intensified the need for efficient lithium (Li) recovery from secondary sources. This study focuses on anti-solvent crystallization for the recovery of high-purity lithium hydroxide monohydrate (LiOH·H₂O) from a Li-rich leachate, derived from the flue dust of a pilot-scale pyrometallurgical process for LIB material recycling. To optimize product yield and purity, a series of experiments were performed, focusing on the influence of parameters such as solvent type, organic-to-aqueous (O/A) volumetric ratio, crystallization time, stirring rate, and anti-solvent addition rate. Acetone was identified as the most effective anti-solvent, producing rectangular cuboid crystals with approximately 90% Li recovery and around 95% purity, under optimized conditions (O/A = 4, 3 h, 150 rpm, and solvent flow rate of 5 mL/min). The flow rate influenced crystal morphology and impurity entrapment, with 5 mL/min favoring nucleation-dominated crystallization regime, producing ~20 μm of well-dispersed crystals with reduced impurity incorporation. SEM-EDS, surface washing, and gradual dissolution of obtained LiOH·H₂O crystals revealed that the impurities sodium (Na), potassium (K), aluminum (Al), calcium (Ca) and chromium (Cr) were crystallized as conglomerates. It was found that Na, K, Al, and Ca primarily crystallized as highly soluble conglomerates, while Cr was crystallized as a lowly soluble conglomerate impurity. In contrast Zn was distributed throughout the crystal bulk, suggesting either the entrapment of soluble zincate species within the growing crystals or the formation of mixed Li-Zn phase. Therefore, to achieve battery-grade purity, further purification measures are necessary. Full article

ZnAl and ZnAlCe layered double hydroxide (LDH) conversion layers modified with picolinoyl N4-phenylthiosemicarbazide (HL) are fabricated on hot-dip galvanized steel (HDG) to improve corrosion protection. X-ray diffraction (XRD) confirms that HL molecules are not intercalated within the LDH interlayers, whereas Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and energy-dispersive X-ray spectroscopy (EDS) analyses reveal their surface adsorption. Moreover, scanning electron microscopy (FE-SEM) observations reveal that HL modification induces changes in surface morphology. After 168 h in 0.1 M NaCl, the LDH structure remains intact, and N and S signals are still detected, confirming the persistence of both the LDH layer and adsorbed HL molecules under corrosive conditions. During 168 h immersion in NaCl, electrochemical measurements indicate that the modified LDH layers exhibit higher corrosion resistance than the unmodified ones, with the ZnAlCe LDH/HL coating providing the most effective protection. Full article