Corrected Debye-Hückel analysis of surface complexation; III. Spherical particle charging including ion condensation

Statistical mechanics has been used to derive a model for the charging of a spherical particle in a salt solution to complement our experimental studies and gain a deeper understanding of the processes involved in surface complexation. Our chosen model goes beyond the equilibrium constants and the Gouy-Chapmann theory currently used in surface complexation models. The proton adsorption is taken to occur at a harmonic potential well on the surface characterized by a frequency v and a well depth u(0). Outside the particle surface there is a capacitor layer of width w(c) which is impenetrable to the salt ions. The diffuse screening of the charged particle is described by a corrected Debye-Hückel analysis accounting for ion size in the ion-ion interactions. To account also for nonlinear electrostatic response a layer of condensed counterions has been introduced. The criterion for the onset of ion condensation is that the electrostatic field exceeds a linear response criterion. Ion size effects are accounted for in terms of hole-corrected electrostatic energies and excluded volume. The model has been applied to titrated surface charge data on goethite (alpha-FeOOH) at various background concentrations and good agreement between the experimental data and the model was obtained. Both the size of the screening ions and the central particle size were shown to be of importance for the surface charge.     

Flexible polyfluorinated bis-diazirines as molecular adhesives

Motivated by a desire to develop flexible covalent adhesives that afford some of the same malleability in the adhesive layer as traditional polymer-based adhesives, we designed and synthesized two flexible, highly fluorinated bis-diazirines. Both molecules are shown to function as effective crosslinkers for polymer materials, and to act as strong adhesives when painted between two polymer objects of low surface energy, prior to thermal activation. Data obtained from lap-shear experiments suggests that greater molecular flexibility is correlated with improved mechanical compliance in the adhesive layer.

Flexible, highly fluorinated covalent adhesives are synthesized, and are shown to afford comparable C–H insertion efficiency and adhesion strength relative to a rigid analogue, while providing improved mechanical compliance in the adhesion layer.     

Photocatalytic Activity of Supported Metal Nanoparticles and Single Atoms

Photocatalysis has been known as one of the promising technologies due to its eco-friendly nature. However, the potential application of many photocatalysts is limited owing to their large bandgaps and inefficient use of the solar spectrum. One strategy to overcome this problem is to combine the advantages of heteroatom-containing supports with active metal centers to accurately adjust the structural parameters. Metal nanoparticles (MNPs) and single atom catalysts (SACs) are excellent candidates due to their distinctive coordination environment which enhances photocatalytic activity. Metal-organic frameworks (MOFs), covalent organic frameworks (COFs) and carbon nitride (g-C₃N₄) have shown great potential as catalyst support for SACs and MNPs. The numerous combinations of organic linkers with various heteroatoms and metal ions provide unique structural characteristics to achieve advanced materials. This review describes the recent advancement of the modified MOFs, COFs and g-C₃N₄ with SACs and NPs for enhanced photocatalytic applications with emphasis on environmental remediation.     

Bernstein operational matrix of fractional derivatives and its applications

In this paper, Bernstein operational matrix of fractional derivative of order α in the Caputo sense is derived. We also apply this matrix to the collocation method for solving multi-order fractional differential equations. The numerical results obtained by the present method compares favorably with those obtained by various collocation methods earlier in the literature.     

Green synthesis of ZnCo<Subscript>2</Subscript>O<Subscript>4</Subscript> nanoparticles by <Emphasis Type="Italic">Aloe albiflora</Emphasis> extract and its application as catalyst on the thermal decomposition of ammonium perchlorate

This work aimed the evaluation of pH influence in the obtainment of composites from palygorskite (PAL) and chitosan (CS). The materials PAL/CS-1 and PAL/CS-2 were obtained by similar methodology with modified pHs: 5.0 ± 0.5 and 11.0 ± 0.5, respectively. Both materials were evaluated for specific surface area analysis, elemental analysis, XRD, FTIR, thermal analysis, MEV and interaction drug composite, using 5-aminosalicylic acid (5-ASA) as model. The surface area analysis data showed the reduction in PAL/CS-2 related to CS presence on surface in contrast with PAL/CS-1, which corroborate with elemental analysis present nine times more of CS in PAL/CS-2 composition. Regarding to XRD data, the interaction of CS with PAL did not cause modification in clay structure in PAL/CS-2. These results were confirmed by FTIR data with the N–H deformation vibration in PAL/CS-2 while PAL/CS-1 was invariable to PAL. In thermal analysis, results were observed 60.2% residual mass to PAL/CS-2, which it was lower than PAL (87.2%) and PAL/CS-1 (86.7%), due to CS decomposition which had enthalpy energy of 62.1 J g^?1 K^?1, confirming the data previously cited. PAL/CS-2 presented 5-ASA adsorption of 7.9 mg g^?1, which was inferior to others probably caused by scarcity of active sites of PAL already occupied by CS. These results showed that pH control was fundamental to enhance efficiency of obtainment of composite in basic pH because the decrease in CS protonation degree increasing interaction between this one and PAL, although it contributed to decrease in 5-ASA adsorption due to low availability of interaction sites.     

Silver(I)‐N‐heterocyclic carbene complexes of bis‐imidazol‐2‐ylidenes having different aromatic‐spacers: synthesis,crystal structure,and in vitro antimicrobial and anticancer studies

A series of Ag(I) complexes ( 6 , 7 , 8 , 9 ) derived from imidazol‐2‐ylidenes was synthesized by reacting Ag₂O with an o‐, m‐, p‐xylyl or 1,3,5‐triazine‐linked imidazolium salts ( 1 , 2 , 3 , 4 ) and then characterizing these using various spectro‐analytical techniques. Additionally, triazine‐linked bis‐imidazolium salt 5 was characterized using the single‐crystal X‐ray diffraction method. Complexes 6–9 were formed from the N‐heterocyclic carbene ligand precursors 1–3 as PF₆^‐ salts in good yields. Conversely, salt 5 does not form Ag(I) complex even under various reaction conditions. Using ampicillin as a standard, complexes 6–9 were tested against bacteria strains Escherichia coli and Staphylococcus aureus as Gram‐negative and Gram‐positive bacteria, respectively, showing potent antimicrobial activities against the tested bacteria even at minimum inhibition concentration and bacterial concentration levels. Furthermore, the potential anticancer activities of the reported complexes were evaluated against the human colorectal cancer (HCT 116) cell lines, using 5‐fluorouracil as a standard drug. The highest anticancer activities were observed for complex 8 with an IC₅₀ value of 3.4 μm , whereas the lowest was observed for complex 9 with an IC₅₀ value of 18.1 μm . Copyright © 2013 John Wiley & Sons, Ltd.     

Solvent Free Synthesis of Coumarins

An efficient synthesis of 3-substituted coumarins under solventless system is described.     

Fundamental solution of generalized thermo-viscoelasticity using the finite element method

The present paper is aimed at an investigation of the temperature, displacement, and stress in a viscoelastic half space of Kelven–Voigt type. The formulation is applied according to three theories of generalized thermoelasticity: Lord–Shulman with one relaxation time, Green–Lindsay with two relaxation times, as well as the coupled theory. The nondimensional governing equations are solved by the finite element method. Numerical results for the temperature distribution, displacement, and thermal stress are represented graphically. Comparisons are made with the results predicted by the CD, L-S, and G-L theories in the presence and absence of the viscoelastic relaxation time.