Mesoporous Bioglasses Enriched with Bioactive Agents for Bone Repair, with a Special Highlight of María Vallet-Regí’s Contribution

Throughout her impressive scientific career, Prof. María Vallet-Regí opened various research lines aimed at designing new bioceramics, including mesoporous bioactive glasses for bone tissue engineering applications. These bioactive glasses can be considered a spin-off of silica mesoporous materials because they are designed with a similar technical approach. Mesoporous glasses in addition to SiO2 contain significant amounts of other oxides, particularly CaO and P2O5 and therefore, they exhibit quite different properties and clinical applications than mesoporous silica compounds. Both materials exhibit ordered mesoporous structures with a very narrow pore size distribution that are achieved by using surfactants during their synthesis. The characteristics of mesoporous glasses made them suitable to be enriched with various osteogenic agents, namely inorganic ions and biopeptides as well as mesenchymal cells. In the present review, we summarize the evolution of mesoporous bioactive glasses research for bone repair, with a special highlight on the impact of Prof. María Vallet-Regí´s contribution to the field.

Effective Dehydration of Fructose Over Stable Ti-Doped SBA-15 Catalysts

High-effective synthesis of 5-hydroxymethylfurfural (HMF) from carbohydrates is an interesting reaction among biomass valorization. The as-synthesized Ti-SBA-15 catalysts with mesoporous structures showed high catalytic efficiency for the conversion of fructose to HMF. Ti-SBA-15 catalysts with different Si/Ti ratios were characterized by characterization techniques such as elemental analysis, XRD, TEM, N2 adsorption–desorption, NH3-TPD, and pyridine-FTIR. The acidity of Ti-SBA-15 catalysts could be tuned by altering addition amount of titanium. The effects of reaction conditions, including reaction time, temperature, and amount of catalyst, on the conversions of fructose and the yields of HMF were also investigated. It is found that Ti-SBA-15 catalysts whose Si/Ti ratio is 120 gave the best yields of HMF, which demonstrated 100% conversion of fructose with a maximum HMF yield of 82% at 140°C after 1 h. In addition, its catalytic performance was retained after 5 recycles in fructose conversion reaction, proving its good catalytic stability.

Surface engineering of Ti3C2Tx MXene by oxygen plasma irradiation as room temperature ethanol sensor

In this work, a surface modification strategy by oxygen plasma irradiation was introduced for the first time to significantly improve the room temperature sensing performance of Ti3C2T[Formula: see text] MXene. Oxygen plasma irradiation induced TiO2 formation on the Ti3C2T[Formula: see text] surface, produced lattice distortion, increased the specific surface area, and provided mesoporous structures. The gas sensitivity performance characterization results show the gas response value of Ti3C2T[Formula: see text] irradiated for 0.5 h (Ti3C2T[Formula: see text]0.5P) was hundreds of times better than the pristine Ti3C2T[Formula: see text]alongside with its sufficient response time (280 s) and rapid recovery time (11 s). The excellent sensing performance is attributed to the formation of more reactive sites on the edge and basal planes of Ti3C2T[Formula: see text] and mesoporous structures which greatly improved the adsorption of ethanol. Additionally, the relatively low work function of TiO2 facilitates the formation of a Schottky junction for easy migration of charge carrier, the thereby shortening the sensing response time. This strategy offers a facile and controllable surface modification of other 2D materials, without damaging their structures.

Sensitive chemoselectivity of cellulose nanocrystal films

Cellulose nanocrystals (CNCs) self-assembled into a chiral nematic structure film is an advanced platform for the fabrication of fascinating sensing, photonic and chiral nematic materials. Despite extensive progress in the functions of CNCs, their chemoselectivity has rarely been reported. Here, we exploit a brand-new perspective of CNCs in chemoselectivity, which shows sensitive selectivity even between isomers of monosaccharides and disaccharide by generating discernible crystal patterns. This sensitive selectivity of glucose homologs is attributed to the selective interaction of carbohydrate–carbohydrate, which enables the tune of the photonic properties and chiral mesoporous structures. Moreover, based on the chemoselectivity, chiral mesoporous structures with tunable specific surface areas are assembled from CNC suspensions and glucose homologs. We envision that the sensitive chemoselectivity of CNC films could provide insights into the recognition of carbohydrates and the preparation of mesoporous carbon in numerous practical applications.

Micro-mesoporous modified activated carbon from corn husks for removal of hexavalent chromium ions

Modified activated carbon sorbents (ACP-Zn and ACP-Zn-Fe) had been prepared from the activation of corn husks precursor to increase the chemical activity of the resulting adsorbents by increasing the number of active functional groups and generation of micro-mesoporous structures. Fourier transform infrared (FTIR) assessed the acidic surface properties of the prepared activated carbons that is due to the presence acidic functional groups such as –OH and –COOH which improves the removal efficiency of the produced sorbents. Textural characteristics revealed the generation of micro-mesoporous structures in ACP–Zn and ACP-Zn-Fe. Thus the combination of H3PO4 with Zn or Zn–Fe could enhance the mesoporosity with a considerable decrease in the adsorption of nitrogen. However, the formation of mesopores might be attributed to the template-like effects of the obtained Zn- of Zn-Fe compounds inside the carbon structure. These structures were employed as sorbents for removal of hexavalent chromium Cr(VI) ions from its aqueous solutions, and the removal efficiency reached ~ 86% for ACP-Zn-Fe and ~ 82% for ACP-Zn. The kinetic modeling studies revealed that the sorption process follows the pseudo-second-order model which indicates that the mechanism of process is chemisorptions. Freundlich, Langmuir and Dubinin–Radushkevich (D–R) models were used to express the experimental data. The isotherm modeling studies revealed that the sorption process was fit with both Freundlich and Langmuir models with maximum capacity 24.8 and 30.3 mg/g for ACP-Zn and ACP-Zn-Fe, respectively.

Modeling of sorption kinetics of U(VI) micro-quantities nanostructured materials with anatase mesoporous structures

The sorption kinetics of uranyl ions micro-quantities from fluoride solutions by nanostructured materials with anatase mesoporous structures has been studied. Using the model of competitive sorption of ions and positively charged complexes of uranyl ion on deprotonated hydroxyl groups of an anatase, kinetic curves of changes in the ratio of ionic forms of uranium in solution were calculated. Modeling was carried out under the assumption of a two-stage mechanism of uranium complex ions sorption. The modeling considered the influence of the uranyl ion carbonate complexes formation. The shift in equilibrium among ionic forms of uranyl correlates with the stability of the complexes in solution.

Molecular Bottom-Up Approaches for the Synthesis of Inorganic and Hybrid Nanostructures

Chemical routes for the synthesis of nanostructures are fundamental in nanoscience. Among the different strategies for the production of nanostructures, this article reviews the fundamentals of the bottom-up approaches, focusing on wet chemistry synthesis. It offers a general view on the synthesis of different inorganic and hybrid organic–inorganic nanostructures such as ceramics, metal, and semiconductor nanoparticles, mesoporous structures, and metal–organic frameworks. This review article is especially written for a wide audience demanding a text focused on the basic concepts and ideas of the synthesis of inorganic and hybrid nanostructures. It is styled for both early researchers who are starting to work on this topic and also non-specialist readers with a basic background on chemistry. Updated references and texts that provide a deeper discussion and describing the different synthesis strategies in detail are given, as well as a section on the current perspectives and possible future evolution.