Ferroelectric Properties of Polymer-Semiconductor Hybrid Material or Composite under Optical Excitation.

Polymer-semiconductor hybrid materials or composites have been investigated with respect to their microstructure, optical, photoconductive, and ferroelectric properties. For this purpose, either CdSe quantum dots or (Cd:Zn)S microparticles were dispersed in poly(vinylidenefluoride-trifluoroethylene) solution and hot pressed to films. In both material systems, the electrical conductivity and the polarization behavior could be controlled by the intensity of the optical excitation. The simultaneous high optical transparency of the CdSe quantum-dot-based hybrid materials makes them particularly interesting for applications in the field of flexible, high-resolution sensors.

Sensing of chemical oxygen demand (COD) by amperometric detection-dependence of current signal on concentration and type of organic species.

The standard method to determine chemical oxygen demand (COD) with K2Cr2O6 uses harmful chemicals, has a long analysis time, and cannot be used for on-site online monitoring. It is therefore necessary to find a fast, cheap, and harmless alternative. The amperometric determination of COD on boron-doped diamond (BDD) electrodes is a promising approach. However, to be a suitable alternative, the electrochemical method must at least be able to determine the COD of water samples independently of the contained substances. Therefore, the current signal as a function of various organic materials was investigated for the first time. It was shown that the height of the signal current depended on the type of organic matter in single-substance solutions and that this substance dependency increases with the amount of COD. Those findings could be explained by the mechanism proposed for this reaction, showing that the selectivity of the reaction depends on the ratio of the concentration of hydroxyl radicals and organic species. We give an outlook on how to improve the method in order to increase the linear working range and avoid signal variance and how to further explain the signal variance.

Influence of chemical structure of organic micropollutants on the degradability with ozonation.

The increasing environmental problems due to various organic micropollutants in water cause the search of suitable additional water treatment methods. Gaining experimental data for the large amount and variety of pollutants would consume a lot of time as well as economic and ecologic resources. An alternative approach is predictive quantitative structure-property relationship (QSPR) modeling, which establishes a correlation between the structural properties of a molecules with a biological, physical, or chemical property. Therefore, in this study, QSPR modeling has been conducted using extensive validation techniques and statistical test to investigate the structural influence on the degradability of organic micropollutants with ozonation. In contrast to most of the other studies, the underlying dataset - rate constants for 92 organic molecules - were obtained under standardized conditions with defined experimental parameters. QSPR modeling was executed using a combination of the software PaDEL for descriptor calculation and QSARINS for the modeling process respecting all five OECD-requirements for applicable QSAR/QSPR-models. The final model was selected using a multi-criteria decision-making tool to evaluate the model quality based on all calculated statistical quality parameters. The model included 10 selected descriptors and fingerprints and showed good regression abilities, predictive power, and stability (R² = 0.8221, CCCtr = 0.9024, Q²loo = 0.7436, R²ext = 0.8420, Q²F1 = 0.8104). The applicability domain of the QSPR model was defined and an interpretation of selected model descriptors has been connected to previous experimental studies. A significant influence of the interpretable descriptors was put into experimental context and compared with previous studies and models. For example, the molar refractivity as a measure of size and polarizability of a molecule and the occurrence of important substructures such as a formamide group seem to decrease the removal rate constant. The contribution of lone electrons entering into resonance as well as the occurrence of fused rings were identified as influences for the increase of the degradability of micropollutants by ozonation.

Prediction of degradability of micropollutants by sonolysis in water with QSPR - a case study on phenol derivates.

The increasing quantity and variety of organic contaminants discharged into surface and groundwater increase the necessity of additional and suitable water treatment methods, which can be incorporated into existing wastewater treatment plants. The huge variety of micropollutants and local variability of the composition of the organic load or matrix effects paired with multiple possible degradation processes lead to the requirement of a recommendation tool for the best possible water treatment method under given local conditions. Due to the diversity of physicochemical properties of micropollutants, such predictions are challenging. In this study, a quantitative correlation between the structural properties of certain micropollutants and their degradability using high-frequency sonolysis has been investigated. Therefore, Quantitative Structure-Property Relationship (QSPR) has been applied on a set of phenol derivates. To obtain the kinetic data, all experiments have been conducted in standardized, constant conditions for all 32 investigated phenol derivates. QSPR modelling was then executed using the software PaDEL for descriptor calculation and the software QSARINS for the overall modelling process including genetic algorithm (GA) and multiple linear regression (MLR). The final model consisting of 5 molecular descriptors was selected using a multi-criteria decision-making method based on extensive statistical parameters. The predictive power and robustness of the model was evaluated by means of internal cross validation and external validation using an independent validation set. The final selected model showed very good values for regression abilities, predictive power as well as stability (R2adj = 0.9455, CCCtr = 0.9777, Q2loo = 0.9285, CCCext = 0.9797 and Q2ext-F1 = 0.9711). The applicability domain of the QSPR model was defined based on the Williams plot and Insubria plot. The five OECD principles for the application of QSPR/QSAR modelling in industry and regulation were fulfilled in the whole process to the best of our knowledge, including the collection of the underlying experimental data as well as the entire modelling process. The final QSPR model included the molecular polarity and occurrence of hydrogen bonds as major influences on the reaction rate constants in accordance with previous studies. Nevertheless, potential biases in the selection of these descriptors due to the small size of the dataset were highlighted.

Refining of Precious Metal Bearing Materials from Secondary Sources-Methanesulfonic Acid Leaching of Raw Silver Granules as a Promising Approach towards a Green Way of Silver Refining.

The state-of-the-art technology of raw silver refining in a silver nitrate-based electrorefining process (Moebius-electrolysis) is accompanied by several disadvantages, both from a technological and from an ecological point of view. In addition, increasing concentrations of critical impurities from secondary sources, like palladium, in raw silver are a further challenge for the future of silver refining. Thus, there is strong motivation for the development of an adequate, alternative process of raw silver refining to substitute the existing Moebius-electrolysis. Due to its less environmentally toxic character and the high aqueous solubility of its silver salt, methanesulfonic acid (MSA) is a possible base chemical for the design of an efficient refining method based on leaching of raw silver followed by electrowinning, with less ecological and technological complications. In this paper the results of some fundamental investigations on the leaching of raw silver granules, containing approx. 94% silver, with methanesulfonic acid and hydrogen peroxide as an oxidation agent are presented. Agitation leaching experiments were conducted on a laboratory scale and the effects of the solid concentration, the hydrogen peroxide dosage and the temperature as leaching parameters were studied. The obtained results indicate that silver leaching yields of more than 90% are achievable with leaching at elevated temperatures of 65 °C or 80 °C, solid concentrations of 500 g/L and at a stoichiometric H2O2:Ag-ratio of 3:1. Increased solid concentrations greater than 500 g/L and elevated temperatures of 65 °C or 80 °C additionally improved the selectivity of the process regarding the leaching of Pd.

Influence of 3d Transition Metal Doping on Lithium Stabilized Na-ß″-Alumina Solid Electrolytes.

Na-ß″-alumina is the commercially most successful solid electrolyte due to its application in ZEBRA and NAS® batteries. In this work, Li-stabilized Na-ß″-alumina electrolytes were doped with 3d transition metal oxides, namely TiO2, Mn3O4, and NiO, in order to improve their ionic conductivity and fracture strength. Due to XRD and EDX measurements, it was concluded that Mn- and Ni-ions are incorporated into the crystal lattice of Na-ß″-alumina. In contrast, TiO2 doping results in the formation of secondary phases that enable liquid-assisted sintering at temperatures as low as 1500 °C. All dopants increased the characteristic fracture strength of the electrolytes; 1.5 wt% of NiO doping proved to be most efficient and led to a maximal characteristic fracture strength of 296 MPa. Regarding the ionic conductivity, TiO2 doping showed the uppermost value of up to 0.30 S cm-1 at 300 °C. In contrast to the other dopants, TiO2 doping lowered the sintering temperature needed to obtain a dense, stable, and highly conductive Na-ß″-alumina electrolyte suitable for applications in Na based batteries.

Sodium Solid Electrolytes: NaxAlOy Bilayer-System Based on Macroporous Bulk Material and Dense Thin-Film.

A new preparation concept of a partially porous solid-state bilayer electrolyte (BE) for high-temperature sodium-ion batteries has been developed. The porous layer provides mechanical strength and is infiltrated with liquid and highly conductive NaAlCl4 salt, while the dense layer prevents short circuits. Both layers consist, at least partially, of Na-ß-alumina. The BEs are synthesized by a three-step procedure, including a sol-gel synthesis, the preparation of porous, calcined bulk material, and spin coating to deposit a dense layer. A detailed study is carried out to investigate the effect of polyethylene oxide (PEO) concentration on pore size and crystallization of the bulk material. The microstructure and crystallographic composition are verified for all steps via mercury intrusion, X-ray diffraction, and scanning electron microscopy. The porous bulk material exhibits an unprecedented open porosity for a NaxAlOy bilayer-system of ≤57% with a pore size of ≈200-300 nm and pore volume of ≤0.3 cm3∙g-1. It contains high shares of crystalline α-Al2O3 and Na-ß-alumina. The BEs are characterized by impedance spectroscopy, which proved an increase of ionic conductivity with increasing porosity and increasing Na-ß-alumina phase content in the bulk material. Ion conductivity of up to 0.10 S∙cm-1 at 300 °C is achieved.

Aluminum Melt Filtration with Carbon Bonded Alumina Filters.

The wetting behavior was measured for Al2O3-C in contact with AlSi7Mg with a conventional sessile drop test (vacuum, 950 °C and 180 min) and a sessile drop test with a capillary purification unit (vacuum, 730 °C and 30 min). The conventional test yielded contact angles of around 92°, whereas the sessile drop measurement with capillary purification showed a strongly non-wetting behavior with a determined apparent contact angle of the rolling drop of 157°. Filtration tests, which were repeated twice, showed that the Al2O3-C filter possessed a better filtration behavior than the Al2O3 reference filter. For both filtration trials, the PoDFA (porous disc filtration analysis) index of the Al2O3-C filter sample was equal to half of the PoDFA index of the Al2O3 reference filter sample, indicating a significantly improved filtration performance when using Al2O3-C filter. Notable is the observation of a newly formed layer between the aluminum and the Al2O3-C coating. The layer possessed a thickness between 10 µm up to 50 µm and consisted of Al, C, and O, however, with different ratios than the original Al2O3-C coating. Thermodynamic calculations based on parameters of the wetting and filtration trials underline the possible formation of an Al4O4C-layer.

Pyrocatalytic oxidation - strong size-dependent poling effect on catalytic activity of pyroelectric BaTiO3 nano- and microparticles.

Pyrocatalysis is an emerging advanced oxidation process for wastewater remediation with the potential for thermal energy harvesting and utilization. Although several studies explored the potential of new pyrocatalyst materials to degrade harmful organic water pollutants, the role of important material properties and electric poling procedures on the pyrocatalytic activity is still unclear. In this work, we investigate the interdependence between particle size, electric poling and pyrocatalytic activity of BaTiO3 powders with nominal particle sizes of 100, 200 and 500 nm by using the dichlorofluorescein redox assay. Depending on the particle size, the influence of surface area or phase composition on the pyrocatalytic activity predominates. Moreover, we demonstrate that poling of pyrocatalysts leads to a strong size-dependent increase of pyrocatalytic activity. This poling effect increases with particle size up to +247% and can be explained with size-dependent changes in phase composition and domain structure. Combining all results, the progression of the pyrocatalytic activity as a function of particle size was derived and a future strategy for maximizing the catalytic performance of pyrocatalysts was developed. This study greatly improves the understanding about the role of important material properties and electric poling on pyrocatalytic activity, thus enabling an effective catalyst design. With the help of highly active catalysts, the pyrocatalytic process can take the next step in its development into a new and energy-efficient advanced oxidation process for water remediation.

The sorption behaviour of amine micropollutants on polyethylene microplastics - impact of aging and interactions with green seaweed.

Microplastics are ubiquitous in the environment. Due to still rising global production, the emission of polymers into the environment and the abundance of microplastics have increased accordingly. Due to the long mineralization processes of microplastics, distribution in all compartments can be found. The hydrophobic surfaces of the particles can sorb chemical pollutants, therefore providing a potential pathway to accumulation by organisms within the food web. However, little is known about how long-term aging and degradation processes of microplastics can affect the sorption behaviours of organic pollutants on the particles. In this study, important industrial additives of emerging environmental concern, such as hydrophobic aromatic amines, were studied in relation to their sorption behaviour on high-density polyethylene and low-density polyethylene microplastics. Diphenylamine (log POW (logarithmic octanol-water partition coefficient) = 3.5) showed strong sorption, carbamazepine (log POW = 2.5) showed moderate sorption, and aniline (log POW = 0.9) showed no detectable sorption behaviour. Artificially aged particles exposed to photochemical aging and long-term mechanical treatment in water were compared to pristine microplastics. While mechanically aged microplastics promoted the sorption of aromatic amines, photochemically aged particles showed a decrease in sorption capacity due to changed surface chemistry. Importantly, the sorption capacity increased with increasing salinity, leading to strong implications for ocean systems, as an elevated uptake of pollutants could occur under marine conditions. Moreover, our study demonstrates that the ecotoxicological effects of diphenylamine on the growth of the seaweed Ulva (sea lettuce, Chlorophyta) were reduced in the presence of microplastics. As the plastic particles withdrew enough contaminants from solution, even toxic levels of diphenylamine (c = 10-4 M) became tolerable for the algae. However, the pollutants initially sorbed on the microplastics can be released again at a later point in the ageing process, thus having delayed pollution potential.

Pyrocatalysis-The DCF assay as a pH-robust tool to determine the oxidation capability of thermally excited pyroelectric powders.

Pyrocatalysis uses thermally excited pyroelectric materials for the generation of reactive oxygen species in water. This unique feature allows it to harvest energy in the form of natural temperature gradients or waste heat from industrial processes in order to degrade organic pollutants at low costs. Its further development into an advanced oxidation process for water remediation is dependent on the availability of pH-robust and nonspecific redox assays for the determination of its oxidation capability. Nevertheless, previous studies neglected the influence of pH changes and they were focused mainly on the degradation of one organic compound or specific chemical dosimetries. In this study, a pH-robust and nonspecific reaction protocol of the dichlorofluorescein assay was established for the investigation of the oxidation capability of the pyrocatalytic process. This reaction protocol was tested on three pyroelectric powders (LiNbO3, LiTaO3, BaTiO3) in different amounts and it overcomes major constraints of a previously used dichlorodihydrofluorescein diacetate-based reaction protocol. Instead of its diacetate, dichlorodihydrofluorescein was used as fluorogenic probe and its concentration was drastically reduced to 1 µM. For the first time, these changes enable the determination and comparison of the oxidation capability independently of pH-rising processes, which are present for all investigated pyroelectric powders up to a pH of 11. Additionally, the precision of the dichlorofluorescein assay was drastically increased and the determination and consideration of autoxidation processes was enabled. Of all three pyroelectric powders, BaTiO3 exhibited the highest oxidation capability with a linear increase with respect to the powder amount.

A novel model for pyro-electro-catalytic hydrogen production in pure water.

The pyro-electro-catalytic induced generation of hydrogen gas is an environmentally friendly and sustainable way to convert excess thermal energy into a storable form. The main idea is to make use of spontaneous polarization of pyroelectric materials that can be altered by temperature changes. Thus, surface potential changes and subsequent electron exchange with surrounding molecules can be induced. In this work, a fundamental model to describe the behavior of a thermally excited pyroelectric material in pure water is developed. The model combines the fields of pyroelectricity, electrochemistry, diffusion and semiconductor theory. After derivation, it was used to explore some basic questions on pyro-electro-catalytic hydrogen production and the accuracy was tested with experimental data. The results show that p/εr has to be balanced depending on the temperature gradient to maximize the hydrogen production. The validation of the experimental data revealed good agreement.

Degradation of endocrine disruptor bisphenol A by ultrasound-assisted electrochemical oxidation in water.

Micropollutants are becoming an increasing problem for the environment and wastewater treatment. One example is Bisphenol A (BPA), an endocrinic disruptor, which is widely used in plastic production. Due to its endocrine disrupting effects on aquatic (micro-)organisms and its ubiquity, in surface- and wastewater alike, adequate treatment techniques are necessary. In this study, the degradation of BPA by a sonoelectrochemical hybrid system was investigated, using a low frequency (24kHz) ultrasound horn and two boron doped diamond electrodes. It was found that by the combination of the individual processes, i.e. ultrasound and electrochemical oxidation, more than 90% of BPA could be removed within 30min at an initial concentration of 1mgL-1. Moreover, synergistic effects were discovered and a considerable improvement compared to the individual processes could be achieved by using a potential of 5V, whereas synergistic effects were absent at a potential of 10V. This study provides investigation of ultrasound amplitude, potential and electrode positioning on BPA degradation. The reaction was found to follow pseudo first order kinetics with a rate constant of 0.089min-1. Samples were analysed by high pressure liquid chromatography (HPLC) using a diode array detector. Moreover, the presence and distribution of hydroxyl radicals within the reactor was visualized by using sonochemiluminescence.