Elsayed M. Zahran

Triazolophanes: a new class of halide-selective ionophores for potentiometric sensors.

Triazolophanes, cyclic compounds containing 1,2,3-triazole units, are a new class of host molecules that demonstrate strong interactions with halides. These molecules are designed with a preorganized cavity that interacts through hydrogen bonding with spherical anions, such as chloride and bromide. We have explored the use of one such triazolophane as a halide-selective ionophore in poly(vinyl chloride) (PVC) membrane electrodes. Different membrane compositions were evaluated to identify concentrations of the ionophore, plasticizer, and lipophilic additive that give rise to the best chloride and bromide selectivity. The lipophilicity of the plasticizer was found to have a great impact on the electrode response. Additionally, the concentration of the lipophilic additive was found to be critical for optimal response. The utility of a triazolophane-based electrode was demonstrated by quantification of bromide in horse serum samples.

Light-activated tandem catalysis driven by multicomponent nanomaterials

Transitioning energy-intensive and environmentally intensive processes toward sustainable conditions is necessary in light of the current global condition. To this end, photocatalytic processes represent new approaches for H2 generation; however, their application toward tandem catalytic reactivity remains challenging. Here, we demonstrate that metal oxide materials decorated with noble metal nanoparticles advance visible light photocatalytic activity toward new reactions not typically driven by light. For this, Pd nanoparticles were deposited onto Cu2O cubes to generate a composite structure. Once characterized, their hydrodehalogenation activity was studied via the reductive dechlorination of polychlorinated biphenyls. To this end, tandem catalytic reactivity was observed with H2 generation via H2O reduction at the Cu2O surface, followed by dehalogenation at the Pd using the in situ generated H2. Such results present methods to achieve sustainable catalytic technologies by advancing photocatalytic approaches toward new reaction systems.

Reactivity of Pd/Fe bimetallic nanotubes in dechlorination of coplanar polychlorinated biphenyls.

A new class of bimetallic materials based on palladium-decorated iron nanotubes is described that demonstrates high reactivity in dechlorination reactions. This high dechlorination efficiency was attributed to the high surface area to volume ratio of the hollow nanotubes structure. Herein, we evaluated the effect of different conditions, such as the nanotube size, and the palladium loading on the efficiency of the dechlorination of PCB 77, a model coplanar polychlorinated biphenyl (PCB), by the Pd/Fe bimetallic nanotubes system. The efficiency of the dechlorination was lowered by decreasing the tube diameter from 200 to 100 nm. In addition, the interior surface as well as the exterior surface of the as-synthesized Pd/Fe bimetallic nanotubes was found to contribute to the high efficiency of the dechlorination of PCB 77. The dechlorination of PCB 77 by Pd/Fe bimetallic nanotubes demonstrated small activation energy indicating diffusion controlled reaction. The as-prepared Pd/Fe bimetallic nanotubes showed extended lifetime activity when used in multiple dechlorination cycles.

Direct Synthetic Control over the Size, Composition, and Photocatalytic Activity of Octahedral Copper Oxide Materials: Correlation Between Surface Structure and Catalytic Functionality

We report a synthetic approach to form octahedral Cu2O microcrystals with a tunable edge length and demonstrate their use as catalysts for the photodegradation of aromatic organic compounds. In this particular study, the effects of the Cu(2+) and reductant concentrations and stoichiometric ratios were carefully examined to identify their roles in controlling the final material composition and size under sustainable reaction conditions. Varying the ratio and concentrations of Cu(2+) and reductant added during the synthesis determined the final morphology and composition of the structures. Octahedral particles were prepared at selected Cu(2+):glucose ratios that demonstrated a range of photocatalytic reactivity. The results indicate that material composition, surface area, and substrate charge effects play important roles in controlling the overall reaction rate. In addition, analysis of the post-reacted materials revealed photocorrosion was inhibited and that surface etching had preferentially occurred at the particle edges during the reaction, suggesting that the reaction predominately occurred at these interfaces. Such results advance the understanding of how size and composition affect the surface interface and catalytic functionality of materials.

Pd-decorated m-BiVO4/BiOBr ternary composite with dual heterojunction for enhanced photocatalytic activity

We introduce a unique material ensemble to boost the photocatalytic activity of m-BiVO4 by creating dual heterojunction of bismuth oxybromide nanosheets and Pd nanodomains. The m-BiVO4/BiOBr/Pd ternary composite demonstrates substantially higher photocatalytic activity compared to pure m-BiVO4. We demonstrate for the first time the use of such visible light photocatalyst in highly efficient degradation of polychlorinated biphenyls.

Can temperature be used to tune the selectivity of membrane ion-selective electrodes?

The selectivity coefficients, KIJpot, of ion-selective electrodes (ISEs) have been fundamentally related to thermodynamic parameters, but yet, the effect of temperature on KIJpot has not been studied. We describe a new approach to fine-tune the selectivity of ISEs based on the effect of temperature on selectivity coefficients. This effect was quantified for ion exchangers as well as neutral carrier ionophores. Potassium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate was used as an ion exchanger in a poly(vinyl chloride) membrane. The corresponding electrode showed an inverse relationship between log KNa+,K+pot and temperature. Additionally, sodium-selective electrodes using monensin, monensin methyl ester (MME), and monensin decyl ester (MDE) were evaluated as models of electrodes based on neutral carriers. The electrode based on monensin showed an enhancement in the selectivity for sodium over potassium by half an order of magnitude as the temperature increased from 20 to 50 degrees C, while the electrodes based on MME or MDE showed a very small change in selectivity. This can be explained in light of changes in the formation constants between the ions and ionophores with temperature. The theory of the effect of temperature on selectivity for both ion exchangers and neutral carrier ionophores is also discussed.

Cyanostar: C–H Hydrogen Bonding Neutral Carrier Scaffold for Anion-Selective Sensors

Cyanostar, a pentagonal macrocyclic compound with an electropositive cavity, binds anions with CH-based hydrogen bonding. The large size of the cyanostars cavity along with its planarity favor formation of 2:1 sandwich complexes with larger anions, like perchlorate, ClO4-, relative to the smaller chloride. We also show that cyanostar is selective for ClO4- over the bulky salicylate anions by using NMR titration studies to measure affinity. The performance of this novel macrocycle as an anion ionophore in membrane ion sensors was evaluated. The cyanostar-based electrodes demonstrated a Nernstian response toward perchlorate with selectivity patterns distinctly different from the normal Hofmeister series. Different membrane compositions were explored to identify the optimum concentrations of the ionophore, plasticizer, and lipophilic additive that give rise to the best perchlorate selectivity. Changing the concentration of the lipophilic additive tridodecylmethylammonium chloride was found to impact the selectivity pattern and the analytical dynamic range of the electrodes. The high selectivity of the cyanostar sensors and their detection limit could enable the determination of ClO4- in contaminated environmental samples. This novel class of macrocycle provides a suitable scaffold for designing various anion-selective ionophores by altering the size of the central cavity and its functionalization.