Gotowa bibliografia na temat „Porous Organic-Inorganic Hybrid Nickle Phosphate Materials”

A hierarchical meso-/macroporous titanium phosphonate (TPPH) hybrid material was prepared via a simple surfactant-assisted process with the use of the precursor tetrabutyl titanate and 1-hydroxy ethylidene-1,1-diphosphonic acid. The prepared hybrid TPPH presented amorphous phase, exhibiting a hierarchical macroporous structure composed of mesopores with a pore size of 2.0 nm. The BET surface area is 256 m2/g. The hydroxyethylidene-bridged organophosphonate groups were homogeneously incorporated in the network of the hierarchical porous solid, as revealed by FT-IR, MAS NMR, XPS, and TGA measurements. The optical properties and photocatalytic activity of the hierarchical TPPH material were investigated in comparison with those of hierarchical porous titanium phosphate and pure mesoporous titania materials, showing superiority of the inorganic-organic hybrid framework, suggesting promising photocatalysts for wastewater cleanup.

The degradation of organic-inorganic hybrid materials based on epoxy resin was characterized electrochemically in aggressive chemical electrolyte. In the present study, the hybrid material as primer was prepared from epoxy resin pigmented by zinc phosphate cured with polyamide (EPZ). The hybrid material was coated on mild steel substrate, and the corrosion behavior was studied by electrode-potential time measurements and mainly by electrochemical impedance spectroscopy (EIS) in 5% NaCl solution. The impedance parameters, namely, coating capacitance (), pore resistance (), charge transfer resistance (), double layer capacitance (), and break point frequency (), corresponding to 45° phase angle as a function of time of exposure were estimated. The observed impedance behavior were compared with the established equivalent electrical circuit represents the coated metal/electrolyte interface. Changes in the values of the circuit components given the information on the stages of degradation and physical phenomenon occurring throughout the degradation of primer coating were also been predicted. In addition, information related to the porous nature of the primer, limited passivation effect, and delamination of coating with longer exposure that resulted in the diffusion controlled corrosion of metal are also recognized. Thus, results indicate that the EPZ coating had good corrosion resistance. This could be a nonpolluting alternative to the traditional chromate like environmentally harmful coatings.

In this work, we evaluated the influence of a novel hybrid 3D-printed porous composite scaffold based on poly(ε-caprolactone) (PCL) and β-tricalcium phosphate (β-TCP) microparticles in the process of adhesion, proliferation, and osteoblastic differentiation of multipotent adult human bone marrow mesenchymal stem cells (ah-BM-MSCs) cultured under basal and osteogenic conditions. The in vitro biological response of ah-BM-MSCs seeded on the scaffolds was evaluated in terms of cytotoxicity, adhesion, and proliferation (AlamarBlue Assay®) after 1, 3, 7, and 14 days of culture. The osteogenic differentiation was assessed by alkaline phosphatase (ALP) activity, mineralization (Alizarin Red Solution, ARS), expression of surface markers (CD73, CD90, and CD105), and reverse transcription–quantitative polymerase chain reaction (qRT-PCR) after 7 and 14 days of culture. The scaffolds tested were found to be bioactive and biocompatible, as demonstrated by their effects on cytotoxicity (viability) and extracellular matrix production. The mineralization and ALP assays revealed that osteogenic differentiation increased in the presence of PCL/β-TCP scaffolds. The latter was also confirmed by the gene expression levels of the proteins involved in the ossification process. Our results suggest that similar bio-inspired hybrid composite materials would be excellent candidates for osteoinductive and osteogenic medical-grade scaffolds to support cell proliferation and differentiation for tissue engineering, which warrants future in vivo research.

Abstract Solvent responsive hydrogel is a kind of intelligent soft material, which can be used in soft robots. Currently, most of the solvent responsive hydrogels are based on pure organic materials which has limited stiffness for actuations. Herein, a novel organic-inorganic composite hydrogel is designed and prepared. Calcium phosphate oligomers (CPO) nanoclusters are incorporated in polymer solution containing polyvinyl alcohol (PVA) and sodium alginate (SA) to form organic-inorganic hybrid copolymer suspensions. The solvent responsive hydrogel is simply prepared using co-evaporation method by optimizing the components in the colloid system. The inorganic nanoparticles work as the scaffold in the porous PVA network and the evaporation caused nonuniformity distribution further induces the formation of heterostructure, which has different shrinkage ratios along the thickness direction. The prepared hydrogel demonstrates excellent shape memory property by changing the environmental solvents between water and ethanol and its repeatability is also verified. The stiffness of hydrogel is enhanced and it has large deformation after incorporation of calcium phosphate nanoparticles. The bending angle of hydrogel can be well controlled by different water to ethanol ratios, allowing for underwater actuation. The functionality of an artificial gripper based on responsive hydrogel with high stiffness is demonstrated to transfer objects in ethanol. The design of organic-inorganic composite hydrogel with high stiffness may provide new insights for preparation of intelligent soft materials for underwater applications.

AbstractOur research is focused on developing inorganic molecular sieve membranes for light gas separations such as hydrogen recovery and natural gas purification, and organic molecular separations, such as chiral enantiomers. We focus on zinc phosphates because of the ease in crystallization of new phases and the wide range of pore sizes and shapes obtained. With our hybrid systems of zinc phosphate crystalline phases templated by amine molecules, we are interested in better understanding the association of the template molecules to the inorganic phase, and how the organic transfers its size, shape, and (in some cases) chirality to the bulk. Furthermore, the new porous phases can also be synthesized as thin films on metal oxide substrates. These films allow us to make membranes from our organic/inorganic hybrid systems, suitable for diffusion experiments. Characterization techniques for both the bulk phases and the thin films include powder X-ray diffraction, TGA, Scanning Electron Micrograph (SEM) and Electron Dispersive Spectrometry (EDS).