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This theoretical investigation delves into the analysis of Reactive red 2 (RR-2) adsorption isotherms on metal hydroxide employing a sophisticated double-layer model characterized by dual-energy levels within the realm of physical adsorption phenomena. An examination of five distinct statistical physics frameworks was undertaken to elucidate the modeling and interpretation of equilibrium data. Expression for the physico-chemical parameters involved in the adsorption phenomena was derived based on statistical physics treatment. Fitting experimental adsorption isotherms (308-333 K) to a DAMTBS has revealed the number of anchored molecules per site, occupied receptor site density, and the number of adsorbed layers. The steric parameter n varies between 0.92 and 1.05. More importantly, it is evidenced that the adhesion mechanism of (RR-2) onto metal hydroxide as determined by the estimated adsorption energies (< 40 kJ/mol) supports a spontaneous and exothermic physisorption process. Thermodynamic potential functions such as entropy, Gibbs free energy, and internal energy have been computed based on the most suitable model. This research advances our physical understanding of how metal hydroxide captures dye molecules RR-2 through adsorption reaction for water depollution treatment.

HighlightsAn efficient and general strategy for ultrafast synthesis of seven transition metal layered hydroxides on conductive substrates is proposed, which avoids the use of additional reagents, multiple steps and long production time in the traditional bottom-up method.The whole synthesis process only takes as fast as approximately 13 s, and its synthesis rate reaches ~ 0.46 cm2 s−1.The NiCo LDH@CC as a demonstration example is selected as cathode material for aqueous alkaline Zn (micro-) battery, which exhibits an outstanding performance.Efficient synthesis of transition metal hydroxides on conductive substrate is essential for enhancing their merits in industrialization of energy storage field. However, most of the synthetic routes at present mainly rely on traditional bottom-up method, which involves tedious steps, time-consuming treatments, or additional alkaline media, and is unfavorable for high-efficiency production. Herein, we present a facile, ultrafast and general avenue to synthesize transition metal hydroxides on carbon substrate within 13 s by Joule-heating method. With high reaction kinetics caused by the instantaneous high temperature, seven kinds of transition metal-layered hydroxides (TM-LDHs) are formed on carbon cloth. Therein, the fastest synthesis rate reaches ~ 0.46 cm2 s−1. Density functional theory calculations further demonstrate the nucleation energy barriers and potential mechanism for the formation of metal-based hydroxides on carbon substrates. This efficient approach avoids the use of extra agents, multiple steps, and long production time and endows the LDHs@carbon cloth with outstanding flexibility and machinability, showing practical advantages in both common and micro-zinc ion-based energy storage devices. To prove its utility, as a cathode in rechargeable aqueous alkaline Zn (micro-) battery, the NiCo LDH@carbon cloth exhibits a high energy density, superior to most transition metal LDH materials reported so far.

In this paper, mixed metal hydroxide (MMH) was prepared via MgCl2 and AlCl3 by the co-precipitation method and characterized by XRD, TGA laser and particle size analysis. The inhibitory effect of MMH on the swelling of clay was evaluated by linear expansion, mud ball, laser particle size analysis, X-ray diffraction analysis and TGA. The linear expansion experiment showed that MMH with a ratio of Mg:Al = 3:1 displayed a strong inhibitory effect on bentonite expansion when 0.3% MMH was added to the drilling fluid, demonstrating better inhibition than 4.0% KCl. Within 48 h, only a few cracks were visible on the mud ball surface in the 0.3% MMH suspension, which indicates that MMH can inhibit wet bentonite for deep hydration. X-ray diffraction and particle size analyses of bentonite were conducted before and after MMH was added to illustrate the inhibition. MMH also displayed high temperature resistance in water-based drilling fluid as a shear strength-improving agent, and its dynamic plastic ratio and shear force were stable after aging at 200 °C for 16 h.

The three-dimensional reference interaction site model theory with the Kovalenko–Hirata closure (3D-RISM–KH) combined with the Kirkwood–Buff integral (KBI) was used to clarify the role of alkali metal hydroxides (MOHs) in cellulose solvation in alkali/urea aqueous solutions. Pair distribution functions, KBI, and the excess number of MOHs showed that M+ hydrates were formed close to cellulose and that their distance was the same as the distance between M+ ions and water molecules in the hydrates. The most stable Li+ hydrate due to the highest Li+ charge density was the closest to the cellulose resulting in the most electrostatic interaction and possibly hydrogen bonding with the cellulose. However, K+ had the lowest charge density, formed the least stable hydrate, and had the least interaction with the cellulose. Hence, the direct solvation energy, which is part of the cellulose solvation energy and accounts for the solute–solvent interaction, was the most negative in the LiOH/urea solution. The solvent reorganization energy—which is another part of the cellulose solvation energy and arises from the clustering of urea, water, and MOH (i.e., ion hydrates) around cellulose—was the most negative in the LiOH/urea solution because of the highest probability and the closest positioning of the Li+ hydrate to the cellulose. Therefore, the calculation results obtained using 3D-RISM–KH and KBI explained the difference among the cellulose solubilities in the LiOH/urea, NaOH/urea, and KOH/urea aqueous solutions.

In order to solve the problem of poor dispersion and stability of mixed metal hydroxide (MMH), a kind of mixed metal hydroxide-like compound (MMHlc) gel was synthesized for use as the base mud in drilling fluid instead of bentonite gel. Na2CO3, Na2SiO3, and C17H33CO2Na were used as precipitants to form MMHlc with larger interlayer spacing and smaller particle size. MMHlc was synthesized by the coprecipitation method at 25 °C with a metal molar ratio of Mg:Al:Fe = 3:1:1. The performance evaluation of the treated drilling fluid showed that MMHlc (S2) synthesized using Na2SiO3 as the precipitant had the characteristics of low viscosity, low filtration, and a high dynamic plastic ratio at 25 °C, which fully met the requirements of oil field application, and it maintained its excellent properties after being aged at 250 °C for 16 h. Linear expansion and rolling recovery experiments showed that the S2 sample had excellent rheological properties and good inhibition. X-ray diffraction and FT-IR experiments showed that S2 had the most complete crystal structure, its interlayer distance was large, and its ion exchange capacity was strong. The thermogravimetric experiment showed that the S2 crystal was stable and the temperature resistance of the crystal could reach 340 °C. Zeta potential, particle size analysis, SEM, and TEM results showed that S2 is a nanomaterial with a complete morphology and uniform distribution. The drilling fluid of this formula had the characteristics of low viscosity, low filtration loss, and a high dynamic plastic ratio, and it met the conditions for oil field application. Considering these results, the new MMH prepared by our research institute is a drilling fluid material that can be used at ultra-high temperatures and can provide important support for drilling ultra-deep wells.

The objective of this paper is to introduce a patented and eco-friendly method to synthesize aqueous suspension of all types of alkaline-earth metal hydroxides nanoparticles (NPs). This method is based on an ion exchange process; the exchange takes place at ambient temperature/pressure, starts from cheap or renewable reagents and, in one single step, results in the creation of the crystalline desired nanoparticles in only a few minutes. In terms of structural and morphological features, the synthesized nanoparticles are characterized by means of XRD-Rietveld refinement, FTIR, and TEM. In particular, we obtained pure and crystalline magnesium and calcium hydroxide suspensions, showing the typical brucite crystal structure with a hexagonal lamellar morphology and dimensions generally <100 nm. With respect to the strontium and barium hydroxide suspensions, we observed different kinds of hydroxides (either anhydrous and hydrate forms), characterized by orthorhombic or monoclinic crystal lattices with rod-like nanostructured morphologies. Despite the different morphologies, all synthesized nanoparticles appear constituted by a superimposition of primary nanoparticles, of dimensions ranging from a few to 15 nm, correlated to the increase in the atomic number of the alkaline earth metal.

This article summarizes our recent developments for H2O2- and O2-based green oxidation reactions by polyoxometalates (POMs) and related compounds. POM-based structurally controlled molecular catalysts exhibit high catalytic performance for epoxidation and sulfoxidation with H2O2. These molecular catalysts can be immobilized on the organic–inorganic hybrid support with covalently anchoring N-octyldihydroimidazolium cation fragments via the anion exchange. In addition, we have developed supported metal hydroxide catalysts such as Ru(OH)x/Al2O3 and Cu(OH)x/TiO2 on the basis of the information of the catalytically active sites with POMs. By using these supported metal hydroxide catalysts, novel aerobic oxidative synthesis of nitriles and amides, and efficient aerobic oxidative homocoupling of alkynes can be realized.

Solid-free drilling fluid has more advantages as a new type of drilling fluid compared with traditional drilling fluid, such as improving drilling efficiency, protecting oil and not having clay particles clog the oil and gas layer. In this study, Zn/Cu/Fe-doped magnesium–aluminum hydroxide (Mg-Al MMH) was prepared using the co-precipitation method and evaluated in solid-free drilling fluid. The inhibition mechanism of synthesized hydroxide was analyzed by X-ray diffraction, laser particle-size analysis and thermogravimetric analysis. The samples were directly used as drilling fluid base muds for performance evaluation. The results showed that the linear expansion rate of 4% M6-Fe was only 12.32% at room temperature within 2 h, that the linear expansion rate was 20.28% at 90 °C and that the anti-swelling rate was 81.16% at room temperature, indicating that it has a strong inhibition ability at both room temperature and at high temperatures. Meanwhile, the possibility of multi-mixed metal hydroxide as a drilling fluid base mud is discussed in this study. We found that 4% M6-Fe exhibited low viscosity, a high YP/PV ratio and high temperature resistance, and its apparent viscosity retention rate reached 100% rolled at 200 °C for 16 h, with a YP/PV ratio of 2.33.

The oxygen evolution reaction is central to making chemicals and energy carriers using electrons. Combining the great tunability of enzymatic systems with known oxide-based catalysts can create breakthrough opportunities to achieve both high activity and stability. Here we report a series of metal hydroxide–organic frameworks (MHOFs) synthesized by transforming layered hydroxides into two-dimensional sheets crosslinked using aromatic carboxylate linkers. MHOFs act as a tunable catalytic platform for the oxygen evolution reaction, where the π–π interactions between adjacent stacked linkers dictate stability, while the nature of transition metals in the hydroxides modulates catalytic activity. Substituting Ni-based MHOFs with acidic cations or electron-withdrawing linkers enhances oxygen evolution reaction activity by over three orders of magnitude per metal site, with Fe substitution achieving a mass activity of 80 A  g catalyst − 1 at 0.3 V overpotential for 20 h. Density functional theory calculations correlate the enhanced oxygen evolution reaction activity with the MHOF-based modulation of Ni redox and the optimized binding of oxygenated intermediates. The oxygen evolution reaction is central to making chemicals and energy carriers using electrons. Metal hydroxide–organic frameworks are shown to act as a tunable catalytic platform for oxygen evolution, with π–π interactions dictating stability and transition metals modulating activity.

The general characteristics of the active center of the catalysts (including zinc-cobalt(III) double metal cyanide complex [Zn-Co(III) DMCC]) for the copolymerization reaction of carbon dioxide (CO2) with epoxide are summarized. By comparing the active center, catalytic performance of the Zn-Co(III) DMCC (and other catalysts) with HCAII enzyme in the organism for activating CO2 (COS and CS2), we proposed that the metal-hydroxide bond (M-OH), which is the real catalytic center of human carbonic anhydride II (HCAII), is also the catalytic (initiating) center for the copolymerization. It accelerates the copolymerization and forms a closed catalytic cycle through the chain transfer reaction to water (and thus strictly meets the definition of the catalyst). In addition, the metal-hydroxide bond catalysis could well explain the oxygen/sulfur exchange reaction (O/S ER) in metal (Zn, Cr)-catalyzed copolymerization of COS (and CS2) with epoxides. Therefore, it is very promising to learn from HCAII enzyme to develop biomimetic catalyst for highly active CO2/epoxide copolymerization in a well-controlled manner under mild conditions.