Fast and Clean Synthesis of Nylon-6/Synthetic Saponite Nanocomposites

Nylon/saponite nanocomposites were synthesized and characterized. The nanocomposites were prepared by means of a fast, efficient, low cost, and environmentally friendly method. All of the tested preparations resulted in the pre-designed nanocomposites. To this end, delaminated saponites were directly synthesized to be used as a filler in a polymer matrix formed by nylon-6 by the in situ intercalation polymerisation of an ε-caprolactam monomer without the use of surfactants or other organic reagents to organophilise the clay, thus avoiding the drawbacks of contamination. The efficiency of the preparation method increased, and significant savings were achieved in terms of both energy reaction time, savings of 60% and 70%, respectively, by using microwave radiation as an energy source during the synthesis of the nanocomposites. In addition, given that the method that was followed avoids the use of contaminating organophilic agents, it is important to highlight the savings in reagents and the fact that there was zero environmental contamination.

Phase Change Materials (PCMs) Based in Paraffin/Synthetic Saponite Used as Heat Storage Composites

Synthetic saponites were successfully used to prepare phase change materials (PCMs) based on paraffin/synthetic saponite. Paraffin/synthetic saponites PCMs were prepared by a solution intercalation process. The PCMs were characterized by powder X-ray diffraction, FT-IR spectroscopy, thermal analyses and nitrogen adsorption. The thermal properties and the stability of PCMs were measured by DSC analysis and from heating–cooling curves. The results showed that the prepared PCMs have a higher heating rate and a lower cooling speed than paraffin because the heat storage was improved with the synthetic saponite. A one-pot synthesis method for obtaining PCM has been successfully developed in this work. The material thus obtained had better results for heat storage applications.

Enhancement of the Luminescence Properties of Eu (III) Containing Paramagnetic Saponite Clays

In this study, 1,10-phenanthroline molecules were introduced in the interlayer space of a paramagnetic synthetic saponite clay containing both Eu3+ and Gd3+ ions in structural positions. Two samples with different loading of phenanthroline dye were prepared. The resulting hybrid materials possessed improved optical emission properties due to an efficient antenna effect from the phenanthroline to the Eu3+ centers; this effect was demonstrated to be higher than the metal-to-metal Gd3+-Eu3+ energy transfer previously studied. Insights on the relaxometric properties in aqueous solution of the solids after incorporation of the antenna groups were also obtained through NMR relaxometric analyses.

Combination of solid-state NMR and 1H NMR relaxometry for the study of intercalated saponite clays with the macrocyclic derivatives of Gd(iii) and Y(iii)

A combination of solid-state NMR and 1H-NMR relaxometric investigations has been employed to characterize the structure and physico-chemical properties of a novel synthetic saponite intercalated with Gd(iii) and Y(iii) chelates.

Novel light-emitting clays with structural Tb3+ and Eu3+ for chromate anion detection

For the first time, Tb3+ and Eu3+ were incorporated into the framework of synthetic saponite by a one-pot hydrothermal procedure, obtaining luminescent materials with interesting photophysical properties, exploited for the fluorescent sensing of the chromate anion in water.

Synthetic saponite clays as promising solids for lanthanide ion recovery

The extraction of lanthanide ions (Ln3+) from aqueous solutions was accomplished with layered materials based on synthetic saponite clays, showing interesting uptake performance and good selectivity.

Synthesis of Saponite Based Nanocomposites to Improve the Controlled Oral Drug Release of Model Drug Quinine Hydrochloride Dihydrate

In the present research study, a 2:1 type of smectite clay minerals, namely natural saponite (NSAP) and synthetic saponite (SSAP), was demonstrated for the first time to be controlled drug release host materials for the model drug quinine hydrochloride dihydrate (QU). The popular sol–gel hydrothermal technique was followed for the synthesis of saponite. The QU was ion exchanged and intercalated into an interlayered gallery of synthetic as well as natural saponite matrices. The developed QU-loaded hybrid composite materials along with the pristine materials were characterized by powder X-ray diffraction (PXRD), Fourier transformed infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA), the Brunauer–Emmett–Teller method (BET) for surface area (SA), and scanning electron microscopy (SEM). The characterization of material results using DSC, FTIR and PXRD confirmed the presence of saponite clay mineral phases in the original and the synthesized saponite samples. Similarly, the drug-loaded composites confirmed the successful intercalation of QU drug on the natural and synthesized saponite matrices. The oral drug release performance of both nanocomposites along with pure quinine drug was monitored in sequential buffer environments at 37 ± 0.5 °C. These composite hybrid materials showed the superior controlled release of QU in gastric fluid (pH = 1.2) and intestinal fluid (pH = 7.4). QU release was best fitted in the Korsmeyer–Peppas kinetic model and demonstrated a diffusion-controlled release from nanocomposite layered materials. The observed controlled drug release results suggest that the applied natural/synthetic saponite matrices have the potential to provide critical design parameters for the development of bioengineered materials for controlled drug release.