Upcycling of post-consumer polyethylene terephthalate bottles into aluminum-based metal-organic framework adsorbents for efficient orthophosphate removal.

2-Phosphonobutane-1,2,4,-tricarboxylic acid (PBTC) is an orthophosphate compound widely used as an antiscalant chemical and corrosion inhibitor in manufacturing. However, PBTC poses persistent environmental concerns due to its stability and resistance to conventional water treatment. In addressing the issues of PBTC in aquatic systems, Al-based metal-organic frameworks (MOFs) have been developed and applied as sustainable adsorbents.

Preparation of heterogeneous cation exchange membrane and its contributions in enhancing the removal of Ni by capacitive deionization system.

Capacitive deionization (CDI), an emerging method to eliminate ions from water at a low cost, has garnered significant interest in recent years. This study evaluates the implication of cation exchange resin loading on the membrane via the nonsolvent-induced phase inversion method. After determining the quantity of resins efficiently loaded on the membrane, it was subsequently utilized as a cation exchange membrane in the membrane capacitive deionization (MCDI) unit to examine the performance removal of Ni.

Synthesis and characterization of Au-decorated graphene oxide nanocomposite for magneto-electrochemical detection of SARS-CoV-2 nucleocapsid gene.

Fast and effective diagnosis is the first step in monitoring the current coronavirus 2 (CoV-2) pandemic. Herein, we establish a simple and sensitive electrochemical assay using magnetic nanocomposite and DNA sandwich probes to rapidly quantify the CoV-2 nucleocapsid (N) gene down to the 0.37 fM level.

Microwave assisted synthesis of MnO nanograins intercalated into reduced graphene oxide layers as cathode material for alternative clean power generation energy device.

MnO nanograins incorporated into reduced graphene oxide as a nanocomposite electrocatalyst have been synthesized via one-step, facile, and single-pot microwave-assisted hydrothermal technique. The nanocomposites were employed as cathode material of fuel cells for oxygen reduction reaction (ORR). The synthesized product was thoroughly studied by using important characterization, such as XRD for the structure analysis and FESEM and TEM analyses to assess the morphological structures of the material.

Multi-function adsorbent-photocatalyst MXene-TiO composites for removal of enrofloxacin antibiotic from water.

MXenes, a new family of two-dimensional transition metal carbides or nitrides, have attracted tremendous attention for various applications due to their unique properties such as good electrical conductivity, hydrophilicity, and ion intercalability. In this work, TiC MXene, or MX, is converted to MX-TiO composites using a simple and rapid microwave hydrothermal treatment in HCl/NaCl mixture solution that induces formation of fine TiO particles on the MX parent structure and imparts photocatalytic activity to the resulting MX-TiO composites. The composites were used for enrofloxacin (ENR), a frequently found contaminating antibiotic, removal from water.

Preparation of Water-Based Alkyl Ketene Dimer (AKD) Nanoparticles and Their Use in Superhydrophobic Treatments of Value-Added Teakwood Products.

A process for preparing emulsions of alkyl ketene dimer (AKD) nanoparticles a nanoemulsion template (emulsion/evaporation) method has been developed. The effects of types and contents of stabilizing agents, , anionic (sodium dodecyl sulfate, SDS), cationic (cetyltrimethylammonium bromide, CTAB), amphoteric (phosphatidylcholine, PC), and polymeric (poly(vinyl alcohol), PVA), on the colloidal stability and hydrodynamic size of the AKD nanoparticles are investigated. The use of 0.

Voltammetric biosensor for coronavirus spike protein using magnetic bead and screen-printed electrode for point-of-care diagnostics.

The rapid spread of the novel human coronavirus 2019 (COVID-19) and its morbidity have created an urgent need for rapid and sensitive diagnostics. The real-time polymerase chain reaction is the gold standard for detecting the coronavirus in various types of biological specimens. However, this technique is time consuming, labor intensive, and expensive.

Dynamic broadening alters triplet extinction coefficients in fluorene oligomers and polymers.

We report T ← T spectra and extinction coefficients, ε, and other properties as functions of chain length for a series of fluorene oligomers, oF, and polymers, pF, with n = 2-84 repeat units. We find that ε increases with length, peaking at 159 400 M cm for oF and then decreases for longer chains. ε does not scale with 1/n or e to reach a constant value at long length, as predicted by the commonly applied oligomer extrapolation approximation, although spectral shifts, oscillator strengths, and transition dipole moments do reach limiting values for chains near 10 units long.

Sudden, "step" electron capture by conjugated polymers.

Data showing significant time-resolution-limited "step" capture of electrons following radiolysis by 7 - 10 ps electron pulses in a series of different length and different concentration conjugated polyfluorene polymers in tetrahydrofuran (THF) are presented. At the highest concentration, ∼48 mM in repeat units for lengths from 20 to 133 fluorenes, ∼30% of the electrons formed during pulse radiolysis were captured in the step, with a constant efficiency per repeat unit. Step capture per repeat unit (q = 6.

Toward designed singlet fission: electronic states and photophysics of 1,3-diphenylisobenzofuran.

Single crystal molecular structure and solution photophysical properties are reported for 1,3-diphenylisobenzofuran (1), of interest as a model compound in studies of singlet fission. For the ground state of 1 and of its radical cation (1(+*)) and anion (1(-*)), we report the UV-visible absorption spectra, and for neutral 1, also the magnetic circular dichroism (MCD) and the decomposition of the absorption spectrum into purely polarized components, deduced from fluorescence polarization. These results were used to identify a series of singlet excited states.

Length and time-dependent rates in diffusion-controlled reactions with conjugated polymers.

Rate constants for diffusion-controlled reactions of solvated electrons with conjugated fluorene oligomers (oF) and polymers (pF) were measured in liquid tetrahydrofuran (THF). Preparative gel permeation chromatography (GPC) was used to separate the polyfluorenes into fractions having narrowed distributions of lengths. Both oF and pF's were used in determinations of the attachment rate constants k(inf) as a function of length, where k(inf) refers to the rate coefficients at long times where they are indeed constant.

Electronic structures of interfacial states formed at polymeric semiconductor heterojunctions.

Heterojunctions between organic semiconductors are central to the operation of light-emitting and photovoltaic diodes, providing respectively for electron-hole capture and separation. However, relatively little is known about the character of electronic excitations stable at the heterojunction. We have developed molecular models to study such interfacial excited electronic excitations that form at the heterojunction between model polymer donor and polymer acceptor systems: poly(9,9-dioctylfluorene-co-bis-N,N-(4-butylphenyl)-bis-N,N-phenyl-1,4-phenylenediamine) (PFB) with poly(9,9-dioctylfluorene-co-benzothiadiazole) (F8BT), and poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) (TFB) with F8BT.

Exciton regeneration at polymeric semiconductor heterojunctions.

Control of the band-edge offsets at heterojunctions between organic semiconductors allows efficient operation of either photovoltaic or light-emitting diodes. We investigate systems where the exciton is marginally stable against charge separation and show via E-field-dependent time-resolved photoluminescence spectroscopy that excitons that have undergone charge separation at a heterojunction can be efficiently regenerated. This is because the charge transfer produces a geminate electron-hole pair (separation 2.