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AbstractSome cases of occurrence of matrix effects (mostly ion suppression) in protein‐precipitated plasma samples, and their influence on the validity of plasma concentrations and pharmacokinetic parameters, are discussed. The comparison of matrix effects using either electrospray (TurboIonspray, TISP) or atmospheric pressure chemical ionization (APCI) indicated that APCI is less prone to matrix effects. Nevertheless, TISP is usually the first choice of ionization technique since unknown thermally labile metabolites might be present in the plasma samples causing erroneous results. A high impact of ion suppression on the plasma concentrations after intravenous (i.v.) administration was found, depending on the drug formulation (vehicle). Since ion suppression caused significantly lower plasma concentrations (by a factor of up to 5.5) after i.v. dosing, the area under the curve (AUC) was underestimated and the plasma clearance was consequently erroneously high, with an impact on drug candidate selection. By simple stepwise dilution (e.g. 10‐fold and 50‐fold) of the supernatant of protein‐precipitated plasma samples, including all calibration and quality control samples, the matrix effects were recognized and eliminated. Copyright © 2003 John Wiley & Sons, Ltd.

The importance of fluorinated products in pharmaceutical and medicinal chemistry has necessitated the development of synthetic fluorination methods, of which direct C–H fluorination is among the most powerful. Despite the challenges and limitations associated with the direct fluorination of unactivated C–H bonds, appreciable advancements in manipulating the selectivity and reactivity have been made, especially via transition metal catalysis and photochemistry. Where transition metal catalysis provides one strategy for C–H bond activation, transition-metal-free photochemical C–H fluorination can provide a complementary selectivity via a radical mechanism that proceeds under milder conditions than thermal radical activation methods. One exciting development in C–F bond formation is the use of small-molecule photosensitizers, allowing the reactions i) to proceed under mild conditions, ii) to be user-friendly, iii) to be cost-effective and iv) to be more amenable to scalability than typical photoredox-catalyzed methods. In this review, we highlight photosensitized C–H fluorination as a recent strategy for the direct and remote activation of C–H (especially C(sp3)–H) bonds. To guide the readers, we present the developing mechanistic understandings of these reactions and exemplify concepts to assist the future planning of reactions.

This study presents 5-hydroxymethylfurfural removal from waste hand paper hydrolysate using activated carbon adsorption. In this context, the effects of adsorbent dosage, initial 5-hydroxymethylfurfural concentration, temperature, and agitation speed on 5-hydroxymethylfurfural adsorption were investigated. Moreover, isotherm and kinetic evaluations were performed using Langmuir, Freundlich, and Temkin models. The experimental data were correlated with zero, first, pseudo-first, and Weber–Morris intraparticle diffusion models. The toxicity of 5-hydroxymethylfurfural was determined using the resazurin reduction assay, and the EC50 of 5-hydroxymethylfurfural in the hydrolysate was found as 192 mg/L. Most convenient 5-hydroxymethylfurfural adsorption was obtained at 5 g/L AC dosage, 40 °C and 150 rpm agitation speed. The highest 5-hydroxymethylfurfural removal efficiency was 92% at 7 g/L AC dosage. The adsorption data fitted best with the Langmuir isotherm model with a maximum uptake capacity of 70.92 mg/g (R2: 0.96). The zero-order reaction kinetic model was the most suitable one among the others inspected. It was determined that intraparticle diffusion was not the rate-limiting step. This study showed that waste hand paper hydrolysate can effectively be detoxified by activated carbon adsorption.

Here, it is discovered that titanate (H2Ti3O7) nanotubes can confine the merger of erythrosin B (ErB) photocatalysis and TEMPO catalysis for highly selective aerobic oxidation of sulfides under irradiation of green light-emitting diodes (LEDs).

The luminescence efficiency of lanthanide-doped upconversion nanoparticles is of particular importance for their embodiment in biophotonic and photonic applications. Here, we show that the upconversion luminescence of typically used NaYF4:Yb3+30%/Tm3+0.5% nanoparticles can be enhanced by ~240 times through a hierarchical active core/active shell/inert shell (NaYF4:Yb3+30%/Tm3+0.5%)/NaYbF4/NaYF4 design, which involves the use of directed energy migration in the second active shell layer. The resulting active core/active shell/inert shell nanoparticles are determined to be about 11 times brighter than that of well-investigated (NaYF4:Yb3+30%/Tm3+0.5%)/NaYF4 active core/inert shell nanoparticles when excited at ~980 nm. The strategy for enhanced upconversion in Yb3+/Tm3+-codoped NaYF4 nanoparticles through directed energy migration might have implications for other types of lanthanide-doped upconversion nanoparticles.

Ultrafast laser-annealing technique for the fabrication of large-grain perovskite films and efficient perovskite solar cells at room temperature.

AbstractA novel multifunctional conjugated polymer (RCP‐1) composed of an electron‐donating backbone (carbazole) and an electron‐accepting side chain (cyanoacetic acid) connected through conjugated vinylene and terthiophene has been synthesized and tested as a photosensitizer in two major molecule‐based solar cells, namely dye sensitized solar cells (DSSCs) and organic photovoltaic cells (OPVs). Promising initial results on overall power conversion efficiencies of 4.11% and 1.04% are obtained from the basic structure of DSSCs and OPVs based on RCP‐1, respectively. The well‐defined donor (D)‐acceptor (A) structure of RCP‐1 has made it possible, for the first time, to reach over 4% of power conversion efficiency in DSSCs with an organic polymer sensitizer and good operation stability.

Abstract Energy harvesting in natural environment has attracted a great deal of attention to generate stable and continuous electrical energy. In this work, we proposed an advanced pyroelectric energy harvesting system by using form-stable phase change material (PCM) composites. The PCM composite connected pyro-electrode generated electrical polarization due to the change of external environment. Polyethylene glycol (PEG) and 1-tetradecanol (1-TD) composites with different phase transition field induced the temperature difference during light-on/-off process. Poly(vinylidene difluoride) (PVDF) was utilized for pyroelectric energy harvesting. The PVDF based pyro-electrode was applied changing the conditions of solar light irradiation and heat air flow. The PCM composites controlled the temperature fluctuation effectively and generated stable output electrical voltage and current. Numerical simulation was carried out to provided in-depth insight into the underlying physics of the system. We envisage that the developed thermal energy harvesting system can pave a way towards high-throughput and sustainable energy harvesting.