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This study focuses on the development of high-performance insulation materials to address the critical issue of reducing building energy consumption. Magnesium-aluminum layered double hydroxides (LDHs), known for their distinctive layered structure featuring positively charged brucite-like layers and an interlayer space, have been identified as promising candidates for insulation applications. Building upon previous research, which demonstrated the enhanced thermal insulation properties of methyl trimethoxysilane (MTS) functionalized LDHs synthesized through a one-step in situ hydrothermal method, this work delves into the systematic exploration of particle size regulation and its consequential effects on the thermal insulation performance of coatings. Our findings indicate a direct correlation between the dosage of MTS and the particle size of LDHs, with an optimal dosage of 4 wt% MTS yielding LDHs that exhibit a tightly interconnected hydrotalcite lamellar structure. This specific modification resulted in the most significant improvement in thermal insulation, achieving a temperature difference of approximately 25.5 °C. Furthermore, to gain a deeper understanding of the thermal insulation mechanism of MTS-modified LDHs, we conducted a thorough characterization of their UV-visible diffuse reflectance and thermal conductivity. This research contributes to the advancement of LDH-based materials for use in thermal insulation applications, offering a sustainable solution to energy conservation in the built environment.

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Over the past decade, the attention of researchers has been drawn to materials with enzyme-like properties to substitute natural enzymes. The ability of nanomaterials to mimic enzymes makes them excellent enzyme mimics; nevertheless, there is a wide berth for improving their activity and providing a platform to heighten their potential. Herein, we report a green and facile route for Tectona grandis leaves extract-assisted synthesis of silver nanoparticles (Ag NPs) decorated on Mg-Al layered double hydroxides (Mg-Al-OH@TGLE-AgNPs) as a nanocatalyst. The Mg-Al-OH@TGLE-AgNPs nanocatalyst was well characterized, and the average crystallite size of the Ag NPs was found to be 7.92 nm. The peroxidase-like activity in the oxidation of o-phenylenediamine in the presence of H2O2 was found to be an intrinsic property of the Mg-Al-OH@TGLE-AgNPs nanocatalyst. In addition, the use of the Mg-Al-OH@TGLE-AgNPs nanocatalyst was extended towards the quantification of Hg2+ ions which showed a wide linearity in the concentration range of 80-400 µM with a limit of detection of 0.2 nM. Additionally, the synergistic medicinal property of Ag NPs and the phytochemicals present in the Tectona grandis leaves extract demonstrated notable antibacterial activity for the Mg-Al-OH@TGLE-AgNPs nanocatalyst against Gram-negative Escherichia coli and Gram-positive Bacillus cereus.

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The decommissioning of uranium mill tailings (UMTs) is usually accompanied by uranium (U) contamination in soil, which poses a serious threat to human health and ecological safety. In this study, a novel phosphorus-modified bamboo biochar (PBC) cross-linked Mg-Al layered double-hydroxide (LDH) composite ("PBC@LDH") was successfully prepared by phosphate pre-impregnation and a hydrothermal method with Mg-Al LDH. Physicochemical analysis revealed that phosphorus-containing functional groups and Mg-Al LDH were grafted onto the pristine biochar (BC) matrix. Laboratory-scale incubation and column leaching experiments were performed on the prepared BC, PBC, and PBC@LDH. The results showed that, at a dosage of 10%, the PBC@LDH composite had a commendable ability to immobilize U in soil. After 40 days of incubation with the stabilizer, the more mobile U was converted into immobilized species. Furthermore, during a column leaching experiment with simulated acid rain, the cumulative loss and leaching efficiency of U were remarkably reduced by PBC@LDH treatment compared with the control, reaching 53% and 54%, respectively. Surface complexation, co-precipitation, and reduction described the adsorption and immobilization mechanisms. In conclusion, this research demonstrates that the PBC@LDH composite offers a potentially effective amendment for the remediation of U contaminated soil.

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A strategy to realize a reinforced photothermal stability cellulose nanofibrils (CNFs) films was reported. The LDHs were dispersed homogeneously onto the active site of CNFs surface by electrostatic self-assembly and the Mg/Al LDHs armour-type nanofibrils were prepared. After simple vacuum filtration, this kind nanofibrils can fabricate highly ordered multilayer film. Suitable amount of additive can bring outstanding photo-thermal property. The visible-light transmittance of the composite films can reach to c.a 80.0% when addition was 0.1% wt. and folding strength of the films contained 0.5% wt LDHs can increased by 15 times. The strength and the light transmittancevery of composite films was also higher than the pure nanocellulose film with the photothermal radiometry for about 30 h under 60 °C drying condition. The production is simple and highly repeatable process could be a good reference for preparation of high photothermal stability and transparent CNFs-based thin films.

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Recently, layered double hydroxides (LDHs) have attracted much consideration due to their versatility and easily manipulating properties and their potential applications such as anion exchangers, support of catalysts, flame retardants, biomedical drug delivery. A novel method for the in-situ preparation in situ of LDHs, using electrocoagulation (EC) processes was developed, the EC process was performed under two different conditions, at 5 mA m-2, changing polarity of the electrodes to find out the composition that leads to LDHs generation. The final product was characterized using XRD, BET and FTIR techniques. This method presented the following advantages: (1) Simultaneously LDHs synthesis and wastewater treatment by ion removal; (2) Polarity control allows to manipulate the M2+/M3+ molar ratio, LDHs properties and its potential applications; (3) The method spent less time to carry out the synthesis and; (4) it did not need complicated solid-liquid separation processes.

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A series of flower-like Mg-Al-layered double hydroxides (FHMA) with four Mg/Al ratios were successfully prepared via a simple method which put the mixed solution of magnesium and aluminum in the mixed solution of water and ethylene glycol (EG). After calcination under 600 °C, the calcination products (CFHMA) were used to adsorb bromate anionic from aqueous solution. The FHMA, CFHMA, and reconstructed CFHMA were characterized by FT-IR, XRD spectra, TG/DTA, N2 adsorption-desorption isotherm, and SEM. It was found that FHMA had the flower-like morphology when Mg/Al ratio was 2 and 3. Moreover, FHMA lost the layered structures during calcination under 600 °C, but the disappeared structures were reconstructed after adsorption of bromate anionic, which was attributed to the "reformation effect" of FHMA with bromate as an interlayer anion. A series of adsorption studies were performed and the mechanism and reactivity of CFHMA were discussed including the effect of different kind of equilibration conditions, such as initial bromate anionic concentration, adsorbent dosage, contact time, initial solution pH, and co-existing anions. The results of adsorption displayed that the most suitable calcination temperature of FHMA is 600 °C, and the best ratio of Mg/Al is 2:1 to remove bromate anionic pollutant from water. The equilibrium adsorption data of CFHMA revealed a good compliance with the Langmuir model and the experimental data of CFHMA fitted well to the pseudo-second-order kinetic model. The calcination product of FHMA was a decent adsorbent of bromate anionic pollutant.

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In the study, two novel applied biocarbon-Mg/Al layered double hydroxides composites (CPLDH and CPLDH-Ca) were successfully prepared and characterized by TEM, ICP-AES, XFS, EDS, FTIR, XRD, BET and pHpzc. The fluoride removal efficiency (RF) and protein recovery ratio (RP) of the adsorbents were studied in protein systems of lysozyme (LSZ) and bovine serum albumin (BSA). The results showed that the CPLDH-Ca presented remarkable performance for selective fluoride removal from protein solution. It reached the maximum RF of 92.1% and 94.8% at the CPLDH-Ca dose of 2.0g/L in LSZ and BSA system, respectively. The RP in both systems of LSZ and BSA were more than 90%. Additionally, the RP of CPLDH-Ca increased with the increase of ionic strengths, and it almost can be 100% with more than 93% RF. Fluoride adsorption by the CPLDH-Ca with different initial fluoride concentrations was found to obey the mixed surface reaction and diffusion controlled adsorption kinetic model, and the overall reaction rate is probably controlled by intra-particle diffusion, boundary layer diffusion and reaction process. The adsorption isotherms of fluoride in BSA system fit the Langmuir-Freundlich model well. The BSA has synergistic effect on fluoride adsorption and the degree increased with the increase of the initial BSA concentration.

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The intercalation of cetirizine into two types of layered double hydroxides, Zn/Al and Mg/Al, has been investigated by the ion exchange method to form CTZAN and CTMAN nanocomposites, respectively. The basal spacing of the nanocomposites were expanded to 31.9 Å for CTZAN and 31.2 Å for CTMAN, suggesting that cetirizine anion was intercalated into Layered double hydroxides (LDHs) and arranged in a tilted bilayer fashion. A Fourier transform infrared spectroscopy (FTIR) study supported the formation of both the nanocomposites, and the intercalated cetirizine is thermally more stable than its counterpart in free state. The loading of cetirizine in the nanocomposite was estimated to be about 57.2% for CTZAN and 60.7% CTMAN. The cetirizine release from the nanocomposites show sustained release manner and the release rate of cetirizine from CTZAN and CTMAN nanocomposites at pH 7.4 is remarkably lower than that at pH 4.8, presumably due to the different release mechanism. The inhibition of histamine release from RBL2H3 cells by the free cetirizine is higher than the intercalated cetirizine both in CTZAN and CTMAN nanocomposites. The viability in human Chang liver cells at 1000 µg/mL for CTZAN and CTMAN nanocomposites are 74.5 and 91.9%, respectively.

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