Prediction of hydroxyapatite crystallite size prepared by sol–gel route: gene expression programming approach

Excellent biocompatibility and its similar biological characteristics to bone apatite, extensively expand the hydroxyapatite (HA) usage in bioimplant applications. The crystallite size of HA is one of the most administrated parameter for determination of reaction rate at the interface of artificial/natural bones. This study tried to propose a new predictive model by employment of the gene expression programming (GEP), i.e., a powerful soft computing technique, to estimate the crystallite size of HA that were prepared by sol–gel route. Firstly, 37 different reliable experiments were carried out considering the type of phosphor precursor, pH, drying temperature, aging time, temperature and time of calcination as practical parameters as input variables, and HA crystallite size as output variable. Absolute fraction of variance (R²), mean absolute percentage error (MAPE), root relative squared error (RRSE), and mean squared error (MSE) were considered to validate the most appropriate GEP model/s. The experiment results were divided randomly into 29 training sets and 8 testing sets. Finally, the best model was selected in R²?=?0.9929, MAPE?=?2.8, RRSE?=?0.0956, and MSE?=?1.7. The results of simulation confirmed the unique features of GEP for the determination of HA crystallite size prepared by sol–gel route.

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Predicted vs. experimental HA crystallite size through GEP-3, GEP-8 and GEP-6 models in (a) training phase, and (b) testing phase.

     

Study of Polypyrrole/Graphene Oxide Nanocomposite Structural and Morphological Changes Including Porosity

Polypyrrole/graphene oxide (PPy/GO) nanocomposite films were electrochemically synthesized to study their structural features. For this purpose, pyrrole monomer was exposed to oxidation in an aqueous dilute solution containing definite amounts of GO and a dopant electrolyte. Potentiostatic electropolymerization was carried out and the current-time curves were obtained for each electrodeposition test. Accordingly, a number of appropriate characterization analyses such as mercury porosimetry, TGA, SEM, XRD, Raman and FTIR spectroscopies were performed in order to investigate the composition and structure of the films. In this regard, factors such as incorporation of GO in the polymer matrix, porous layer structure and the thickness of the films were determined. The results showed that GO concentration could influence on both film thickness and its porous structure. Also, it was observed that the main factor controlling the film thickness and morphology is the potential applied.     

Sulfamic acid: an efficient, cost-effective and recyclable solid acid catalyst for the three-component synthesis of α-amino nitriles

α-Amino nitriles are synthesized by the three-component coupling reaction of aldehydes, amines and trimethylsilyl cyanide using sulfamic acid as a heterogeneous solid acid catalyst, under solvent-free conditions in excellent yields. The catalyst was recovered by simple filtration and was recycled in subsequent reactions.     

N-tert-Butoxycarbonylation of amines using H3PW12O40 as an efficient heterogeneous and recyclable catalyst

The commercially available heteropoly acid H₃PW₁₂O₄₀ (0.5 mol %) is a very efficient and environmentally benign catalyst for N-tert-butoxycarbonylation of amines (primary, secondary) with di-tert-butyl dicarbonate at room temperature in short reaction times (<10 min). No competitive side products such as isocyanates, ureas, N,N-di-tert-butoxycarbonyls, O-Boc and oxazolidinones were observed. Chiral α-amino alcohols and esters afforded the corresponding N-Boc derivatives chemoselectively in excellent yields.     

The first phosphoramide–mercury(II) complex with a Cl2Hg–OP[N(C)(C)]3 segment

Mercury(II) exhibits a strong preference for linear coordination which has been attributed to relativistic effects splitting the 6p orbitals and promoting sp hybridization. If the two ligands attached to the mercury(II) ion are weak donors, the metal ion can act as a good Lewis acid and expand its coordination number. Moreover, mercury has a special affinity for softer bases, such as S and N atoms, and has much less affinity for hard bases, such as those including an O atom. The asymmetric unit of dichlorido[tris(piperidin‐1‐yl)phosphane oxide‐κO]mercury(II)–dichloridomercury(II) (2/1), [HgCl₂{(C₅H₁₀N)₃PO}]₂·[HgCl₂], is composed of one HgCl₂{(C₅H₁₀N)₃PO} complex and one half of a discrete HgCl₂ entity located on an inversion centre. The coordination environment around the Hg^II centre in the complex component is a distorted T‐shape. Bond‐valence‐sum calculations confirm the three‐coordination mode of the Hg^II atom of the complex molecule. The noncovalent nature of the Hg…Cl and Hg…O interactions in the structure are discussed.     

Ether and Relativity

We consider one of the fundamental debates in performing the relativity theory, namely, the ether and the relativity points of view, in a way to aid the learning of the subjects. In addition, we present our views and prospects while describing the issues that being accessible to many physicists and allowing broader views. Also, we very briefly review the two almost recent observations of the Webb redshift and the ultra high energy cosmic rays, and the modified relativity models that have been presented to justify them, wherein we express that these justifications have not been performed via a single model with a single mechanism.     

3D vs. turbostratic: controlling metal–organic framework dimensionality via N-heterocyclic carbene chemistry

Using azolium-based ligands for the construction of metal–organic frameworks (MOFs) is a viable strategy to immobilize catalytically active N-heterocyclic carbenes (NHC) or NHC-derived species inside MOF pores. Thus, in the present work, a novel copper MOF referred to as Cu-Sp5-BF₄, is constructed using an imidazolinium ligand, H₂Sp5-BF₄, 1,3-bis(4-carboxyphenyl)-4,5-dihydro-1H-imidazole-3-ium tetrafluoroborate. The resulting framework, which offers large pore apertures, enables the post-synthetic modification of the C² carbon on the ligand backbone with methoxide units. A combination of X-ray diffraction (XRD), solid-state nuclear magnetic resonance (ssNMR) and electron microscopy (EM), are used to show that the post-synthetic methoxide modification alters the dimensionality of the material, forming a turbostratic phase, an event that further improves the accessibility of the NHC sites promoting a second modification step that is carried out via grafting iridium to the NHC. A combination of X-ray absorption spectroscopy (XAS) and X-ray photoelectron spectroscopy (XPS) methods are used to shed light on the iridium speciation, and the catalytic activity of the Ir–NHC containing MOF is demonstrated using a model reaction, stilbene hydrogenation.

A new MOF with a saturated N-heterocyclic carbene ligand undergoes a series of structural transformations to produce a turbostratic material, which serves as a better support for an iridium hydrogenation catalyst, when compared to the parent material.     

High-Resolution Temporo-Ensemble PIV to Resolve Pore-Scale Flow in 3D-Printed Fractured Porous Media

Transport in Porous Media - Fractures are conduits that can enable fast advective transfer of (fluid, solute, reactant, particle, etc.) mass and energy. Such fast transfer can significantly affect...     

Unsteady motion of a non-linear viscoelastic fluid

In this paper, we study the unsteady flow of a generalized second grade fluid. Specifically, we solve numerically the linear momentum equations for the flow of this viscoelastic shear-thinning (shear-thickening) fluid surrounding a solid cylindrical rod that is suddenly set into longitudinal and torsional motion. The equations are made dimensionless. The results are presented for the shear stresses at the wall, related to the drag force; these are physical quantities of interest, especially in oil-drilling applications.     

Synthesis of polymeric organic-inorganic hybrid materials. Partially deacetylated chitin-silica hybrid

This work reports the synthesis of a novel polymeric organic-inorganic hybrid. The inorganic component is a silica network obtained by controlled hydrolysis of tetraethyl orthosilicate via sol-gel process and the organic counterpart is partially deacetylated chitin (CHI). The resulting polymer hybrids were homogeneous transparent film forming glassy materials being compatible through a wide composition range. Simultaneous thermal analysis of a CHI/silica 1:1 mixture confirms the intermolecular complex formation between organic and inorganic polymers.