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The production of biobased copolymers such as poly(styrene-co-butyl acrylate-co-methacrylic acid) for paints and coating applications is indispensable for the establishment of sustainable biorefine...

IR spectroscopy can be a non-destructive and straightforward probing tool in the battery research. However, its application has been limited due to the difficulties related to the handling and interpretation of ex situ samples along with the lack of widely applicable in situ and operando cells. Herein, we show a simple, operando ATR-IR two electrode pouch cell with an IR-transmissive silicon window and discuss its advantages and limitations. This setup is applied to the study of the polyanthraquinone (PAQ) reaction mechanism in Li- and Mg-organic batteries. During the reduction/oxidation process of the PAQ, not only the conversion of both C O groups into C–O– species is observed, but also the formation of an intermediate semiquinone radical anion as an intermediate product. Furthermore, continuous measurement of IR spectra allows visualization of the gradual solid-electrolyte interphase (SEI) buildup on the cathode during cycling.

Despite the fact that the methanol synthesis process includes industrially some of the most important catalytic chemical reactions, it is still not clear how different gaseous species impact cataly...

Semi-interpenetrating polymer networks (semi-IPNs) were prepared by in situ simultaneous orthogonal polymerizations, where the linear poly(e-caprolactone) (PCL) was synthesized by ring-opening polymerization of e-caprolactone and the poly(styrene-co-divinylbenzene) (PS) network was formed by free-radical polymerization of styrene/divinylbenzene. Semi-IPNs were used as the precursors for the preparation of porous PS monoliths. To this end, the PCL domains were selectively removed by hydrolysis under basic conditions. By changing the amount of organocatalyst used for the ring-opening polymerization of e-caprolactone, the relative polymerization kinetics of both monomers was varied, which has a pronounced effect on the morphology of thus-obtained PS frameworks.

A new species’ class of Cu-, Ga- and Zn-based rate catalysts was prepared by a systematic co-precipitation technique at the different related pH values (6.5–8.0) along with calcination functional conditions, influencing components’ physical properties, these were characterized, and their application performance for water–gas shift (WGS) reaction was researched. Substances were analysed by various experimental methods, namely chemisorption, temperature-programmed reduction (TPR) characterisation, diffraction, physisorption and microscopy. A homogenous size dispersion of the compounds with smaller granular particles was obtained for catalysis, implemented with high pH-resulting outputs. H2 TPR profiles revealed a tailored stronger effect of Cu–Zn on Ga for process, operated with low pH-conditioned forms. Over Cu/ZnGaOX, WGS was sensitive to Cu, which was primarily active. Catalytic chemical reactivity, activity and selectivity were also found to be critically dependent on material lattice structure, copper surface area and metal–support interaction phenomena. The temperature-programmed surface reaction with mass spectrometry (TPSR–MS) measurements showed that formulations, synthesised at the pH of 8.0, enabled reaching >99% of the equilibrium yield CO conversion at 260 °C. An increase in the converted CO, oxidation and H2 productivity with the integral steam content in gaseous feed flow was achieved. The heterogeneous phase processing at the correlated pH of 7.6 demonstrated the highest formed CO product at the temperature of 200 °C, compared with literature. This is particularly promising for reagent purity hydrogen-fed fuel cells. The kinetics for each co-precipitated solid was evaluated regarding the efficiency for the WGS in a fixed bed reactor. Keywords: Syngas, Hydrogen, Cu/ZnGaOX catalyst, Water–gas shift (WGS), Steam reforming reactions, Fuel cell systems

A fast, robust, and convenient method for quantitative determination of polyamide-6 (PA6) and polyamide-66 (PA66) in plastic wastes is presented. The method includes a straightforward procedure for...

Solvent- (SB) and water-borne (WB) fluoropolymer coatings were produced for the outdoor protection of bronze. The coatings were prepared from commercially available resins with alternating fluoroethylene/vinylether copolymers. Because any application of protective coatings on works of art requires that they be removable in accordance with conservation ethics, various approaches to achieve removability of coatings were tested. The influence of modifications was verified through comparisons of hydrophobic, compact and irremovable protective coatings. Consequently, we prepared four types of coatings: two SB coatings and two WB coatings. The first SB coating was designed to have a hydrophobic compact structure (SB-c coating), and the second SB coating was modified with the addition of agents that impart strippability (SB-h coating). The same approach was used for the preparation of the two WB coatings: a compact (WB-c) coating vs. a hydrophilic (WB-h) coating, the latter being prepared through the addition of hydrophilic polyisocyanate. The surface properties of the coatings were compared using scanning electron (SEM) and atomic force (AFM) microscopy. WB coatings were found to be more homogeneous in comparison with SB coatings and to have lower surface roughness. Contact angles confirmed the more hydrophobic nature of SB coatings. Potentiodynamic polarisation measurements and accelerated corrosion tests (exposure to acid vapours) revealed that protection efficiency not only increased with thickness but significantly depended on the coating structure. The structure of coatings depended on the rheological parameters of the formulations simulating their behaviour during storage, deposition, and formation of the dry coating. Combined electrochemical and vibrational spectroscopic experiments were used to simulate long-term outdoor exposure of the protective coatings. Ex situ IR RA spectroelectrochemical measurements showed that hydration was more prevalent with WB coatings, and oxidation of bronze at the interface eventually occurred (656 cm −1 band). WB coatings with more free C O groups were more prone to degradation. In situ Raman spectroelectrochemistry confirmed the better protection efficiency of SB over WB coatings. The optical properties of the coatings on glass showed higher transmittance for WB coatings compared to SB coatings.

The use of rare earth elements is a growing trend in diverse industrial activities, leading to the need for eco-friendly approaches to their efficient recovery and reuse. The aim of this work is the development of an environmentally friendly and competitive technology for the recovery of those elements from wastewater. Kinetic and equilibria batch assays were performed with zeolite, with and without bacterial biofilm, to entrap rare earth ions from aqueous solution. Continuous assays were also performed in column setups. Over 90% removal of lanthanum and cerium was achieved using zeolite as sorbent, with and without biofilm, decreasing to 70% and 80%, respectively, when suspended Bacillus cereus was used. Desorption from the zeolite reached over 60%, regardless of the tested conditions. When in continuous flow in columns, the removal yield was similar for all of the rare earth elements tested. Lanthanum and cerium were the elements most easily removed by all tested sorbents when tested in single- or multi-solute solutions, in batch and column assays. Rare earth removal from wastewater in open setups is possible, as well as their recovery by desorption processes, allowing a continuous mode of operation., This study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the research project PTDC/AAG-TEC/5269/2014, the strategic funding of UID/BIO/04469/2013 unit and BioTecNorte operation (NORTE-01-0145-FEDER-000004) funded by the European Regional Development Fund under the scope of Norte2020 - Programa Operacional Regional do Norte, Portugal., info:eu-repo/semantics/publishedVersion

Two-component solvent-born polyurethane coatings for the protection of bronze from corrosion were prepared. Trisilanol-heptaisooctyl polyhedral oligomeric silsesquixane (POSS) nanoparticles were exploited to increase the coating protective efficiency. Its improvement was confirmed through a combination of characterisation techniques. In particular, the POSS addition caused an increase of the water contact angle, and an enhancement of the elastic connotation and abrasion resistance of the polyurethane coating. Potentiodynamic polarisation measurements also indicated that the coating containing POSS nanoparticles has an improved protection efficiency. Impedance spectroscopy revealed that the magnitude of low-frequency impedance of polyurethane coatings decreased more for the coating without POSS during exposure in electrolyte for thirty days. Ex situ IR reflection-absorption spectroelectrochemistry was exploited to get insight into the degradation of coatings during chronocoulometric charging at anodic potentials. IR reflection-absorption technique was also used to evaluate any possible effect of different stripper solutions on the bronze substrate.

Properties of mixed-metal MOFs depend on the distribution of different metals within their frameworks. Determination of this distribution is often very challenging. Using an example of aluminum- and iron-containing MIL-100, we demonstrate that 27Al NMR spectroscopy, when combined with first-principles calculations and magnetic, X-band electron paramagnetic resonance, Fe K-edge extended X-ray absorption fine structure, and Mössbauer measurements, enables one to accurately determine the arrangement of Al and Fe within the metal trimers, which are the basic building units of MIL-100. In this particular material, the incorporation of Fe and Al on the framework metal sites is random. Crucial for deciphering the arrangement is detecting NMR signals, shifted because of the strong hyperfine interaction between the 27Al nuclei and the unpaired electronic spins of Fe3+ ions, assigning the shifted signals aided by first-principles calculations of hyperfine couplings, and quantitatively evaluating the NMR intensities and the measured effective magnetic moment.