Study of the effect of the LDH cations precursors in the removal of arsenic in aqueous solution

Layered double hydroxides (LDH) are anionic clays, mainly used as adsorbents, ion exchange material, and catalysts. Generally, they present high specific surface areas, alkaline character, high metallic dispersion, and high thermal stability. If they contain a transitional element in their structure, the solid may present redox properties. LDH were synthesized with the following combinations: MgAl, MgFe, and ZnMgFe, aiming to determine the effect of cationic nature in the structure and the functionality of the synthesized clay as adsorbents in polluted aqueous effluents. The textural properties were determined by nitrogen adsorption isotherms. Crystalline structure was studied by XRD and the presence of the anions of the interlayer was determined by FTIR spectroscopy. The studies of removal of As(III) and As(V) from aqueous solutions, using the LDH, show that after 24 h the solids reach a high removal efficiency. ZnMgFe solid removed both species of arsenic with values of 95 and 98% for As(II) and As(V), respectively. The MgFe solid showed some selectivity to the uptake of As(V), while the MgAl only removed As(V). This selective behaviour can be beneficial in studies of arsenic speciation.

Synthesis and Characterization of Layered Double Hydroxides as Materials for Electrocatalytic Applications

Layered double hydroxides (LDHs) are anionic clays which have found applications in a wide range of fields, including electrochemistry. In such a case, to display good performances they should possess electrical conductivity which can be ensured by the presence of metals able to give reversible redox reactions in a proper potential window. The metal centers can act as redox mediators to catalyze reactions for which the required overpotential is too high, and this is a key aspect for the development of processes and devices where the control of charge transfer reactions plays an important role. In order to act as redox mediator, a material can be present in solution or supported on a conductive support. The most commonly used methods to synthesize LDHs, referring both to bulk synthesis and in situ growth methods, which allow for the direct modification of conductive supports, are here summarized. In addition, the most widely used techniques to characterize the LDHs structure and morphology are also reported, since their electrochemical performance is strictly related to these features. Finally, some electrocatalytic applications of LDHs, when synthesized as nanomaterials, are discussed considering those related to sensing, oxygen evolution reaction, and other energy issues.

Magnetic sorption materials for recovery of organic anions from aqueous solutions

Layered double hydroxides (LDHs) belong to the class of two-dimensional anionic clays with a layered structure similar to brucite. The combination of sorption and magnetic properties of layered materials is promising. In this work, magnetic materials based on LDHs (MLDHs) were synthesized and their sorption and magnetic properties were studied. The synthesis of LDHs was carried out by a co-precipitation method followed by calcination. Intercalated Mg, Fe(III)-, Mg, Fe(III), Al-and Mg, Al-LDHs were prepared using LDHs by rehydration in solutions of iron(III) citrate (Cit) or oxalate (Ox) followed by the calcination at 400°C for 2-4 h. LDHs and their thermal decomposition products were characterized by FTIR spectroscopy, laser and X-ray diffraction and thermogravimetry. The sorption experiment was carried out under static conditions using glutamic acid (Glu) as a model organic compound. The maximum sorption capacity of Mg, Fe(III)-LDH and Mg, Al-FeCit-LDH calcined at 400°C was 6.6 and 8.8 mg/g Glu, respectively. The sorption kinetics of intercalated and calcined Mg, Al-and Mg, Fe(III), Al-LDH and calcined at 500º C Mg, Fe(III)-LDH was described by the pseudo-second order model. The magnetic properties of the LDHs and thermal decomposition products were retained after the adsorption of glutamic acid, making it possible to easily separate these MLDHs from the solution by magnetic field.

Effect of LDHs and Other Clays on Polymer Composite in Adsorptive Removal of Contaminants: A Review

Recently, the development of a unique class of layered silicate nanomaterials has attracted considerable interest for treatment of wastewater. Clean water is an essential commodity for healthier life, agriculture and a safe environment at large. Layered double hydroxides (LDHs) and other clay hybrids are emerging as potential nanostructured adsorbents for water purification. These LDH hybrids are referred to as hydrotalcite-based materials or anionic clays and promising multifunctional two-dimensional (2D) nanomaterials. They are used in many applications including photocatalysis, energy storage, nanocomposites, adsorption, diffusion and water purification. The adsorption and diffusion capacities of various toxic contaminants heavy metal ions and dyes on different unmodified and modified LDH-samples are discussed comparatively with other types of nanoclays acting as adsorbents. This review focuses on the preparation methods, comparison of adsorption and diffusion capacities of LDH-hybrids and other nanoclay materials for the treatment of various contaminants such as heavy metal ions and dyes.

New Technological Approach for Glycyrrethic Acid Oral and Topical Administration

Background: 18β- glycyrrhetinic acid (Gly) is the major bioactive component of licorice roots and rhizomes of the Glycyrrhiza glabra species. It shows many activities such as antiviral, anti-inflammatory, antioxidant, antimicrobial, and antifungal, however, its use in the health field is very limited due to the low water solubility. Methods: This paper deals with the development of a new technological approach for Gly dissolution rate enhancement. It consists of Gly intercalation (guest) in the interlamellar spaces between the inorganic spaces (host) of the anionic clays “hydrotalcites” (HTlc) to obtain hybrids MgAl-HTlc-Gly and ZnAl-HTlc-Gly. Gly can find applications in both systemic and local therapies, thus advantages of the use of the hybrids in these two fields were investigated. Results: Gly dissolution rate from hybrids in the intestinal environment, site in which it is preferentially absorbed, resulted enhanced (ZnAl-HTlc-Gly > MgAl-HTlc-Gly) compared to the crystalline form, thereby, making them suitable for oral administration as dry powder in hard capsules. : For a local therapy, bioadhesive, vaginal emulgels loaded with the hybrids were developed. These showed suitable mucoadhesive property to the vaginal mucosa, necessary to prolong the residence time in the application site. The emulgel containing ZnAl-HTlc-Gly showed a faster and higher release profile than that containing MgAl- HTlc-Gly. Conclusions: The obtained results suggest that Gly intercalation into HTlc, especially in ZnAl-HTlc, allows to enhance Gly dissolution when the hybrids are formulated both as oral or topical products.

Synthesis and Physico-chemical Characterization of Nanohybrid Materials Based on Isonicotinic Acid Hydrazide

The usual treatment for tuberculosis is difficult by its long-term therapy, raised dosing frequency and adverse effects of anti-tuberculosis drugs. Anionic clays, also called layered double hydroxides are a class of hydrotalcite like structures having high compositional variety and being able to self-assembly in the presence of drug molecules. The work refers to the development of nanohybrid materials like delivery systems that intercalates isonicotinic acid hydrazide, known as isoniazid anti-tuberculosis drug, into layered structure of hydrotalcite compounds. Loaded drug molecules of isoniazid were proved to be released in a controlled way from the as synthesized nanostructure in a simulated buffer solution. The obtained sample was characterized by advanced techniques thus demonstrating the inclusion of isoniazid antibiotic between hydrotalcite sheets. These results revealed important expectations for further researches of these organic-inorganic nanocomposites for tuberculosis treatment.

Development and Characterization of New Topical Hydrogels Based on Alpha Lipoic Acid—Hydrotalcite Hybrids

Alpha lipoic acid (ALA) is a well-known anti-aging compound. The activity of this molecule is limited by two important factors: (i) The low stability to oxidation and thermal processes and (ii) the low solubility. Particularly the latter limits ALA formulation in hydrophilic bases. The purpose of this paper is to present a new technological approach to stabilize lipoic acid in topical hydrogels for cosmetic use. With this aim, ALA was intercalated in two different lamellar anionic clays (hydrotalcites), MgAl and ZnAl, obtaining the hybrids MgAl-ALA and ZnAl-ALA. The intercalation allows to obtain a more manageable product in comparison to raw ALA. After the preliminary characterization, hydrogels containing the hybrids were prepared and characterized, also in comparison to the commercial product Tiobec® in terms of rheological properties, stability to temperature and centrifugation, release, and cytotoxicity. The obtained results highlighted that the hydrogel containing MgAl-ALA is a suitable alternative to the products currently available on the market.

Understanding the Ion Exchange Process in LDH Nanomaterials by Fast In Situ XRPD and PCA-Assisted Kinetic Analysis

Layered double hydroxides (LDHs) are nanomaterials with interesting properties finding applications in many fields, such as catalysis, environmental chemistry, and pharmaceuticals. They are anionic clays with positively charged layers and anions within the layers to reach neutrality. Their properties are defined by both composition and morphology. The composition can be tuned by exchanging the interlayer anion. The far more stable, common, and highly prevalent among natural LDHs is the carbonate anion thanks to its double negative charge. To adapt the properties of LDHs for technological applications, the challenge is to exchange the carbonate with the functionalizing monovalent anions in an effective and cheap way. In this study, the exchange of carbonate with nitrate ions is studied by in situ X-ray powder diffraction (XRPD). The exchange is carried out by a liquid-assisted grinding approach, inserting the mechanically ground dry sample in a capillary and then wetting it with a drop of nitric acid, while measuring the XRPD pattern. The kinetics of the process was investigated by the Avrami-Erofe’ev method; the reaction mechanism was determined using the advancing interface model and by analyzing the XRD peak shapes, which evidentiate changes in the crystallinity during the reaction. The reaction starts from the faces perpendicular to the layers and occurs along the channels, increasingly limited by diffusion when approaching the internal part of the crystals.