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- Antrodia vaillantii (2)
- Beton (2)
- Betonangriff (2)
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- Copper(II) (2)
- Dauerhaftigkeit (2)
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- Laser-GMA-hybrid welding (2)
Organisationseinheit der BAM
The present work shows results on elemental distribution analyses in Cu(In,Ga)Se2 thin films for solar cells performed by use of wavelength-dispersive and energy-dispersive X-ray spectrometry (EDX) in a scanning electron microscope, EDX in a transmission electron microscope, X-ray photoelectron, angle-dependent soft X-ray emission, secondary ion-mass (SIMS), time-of-flight SIMS, sputtered neutral mass, glow-discharge optical emission and glow-discharge mass, Auger electron, and Rutherford backscattering spectrometry, by use of scanning Auger electron microscopy, Raman depth profiling, and Raman mapping, as well as by use of elastic recoil detection analysis, grazing-incidence X-ray and electron backscatter diffraction, and grazing-incidence X-ray fluorescence analysis. The Cu(In,Ga)Se2 thin films used for the present comparison were produced during the same identical deposition run and exhibit thicknesses of about 2 µm. The analysis techniques were compared with respect to their spatial and depth resolutions, measuring speeds, availabilities, and detection limits.
Two new octahedral cluster complexes [Re6S8(3,5-Me2PzH)6]Br2 · 2(3,5-Me2PzH) (1) and [Re6Se8(3,5-Me2PzH)6]Br2 · 2(3,5-Me2PzH) (2), where 3,5-Me2PzH is 3,5-dimethylpyrazole, have been synthesized using reaction of rhenium chalcobromide complexes Cs4[Re6S8Br6] · 2H2O and Cs3[Re6Se8Br6] · H2O, respectively, with molten 3,5-dimethylpyrazole. Both compounds synthesized were characterized by X-ray single-crystal diffraction and chemical analysis, IR and luminescent spectra.
Darstellung und Charakterisierung von Nanopartikeln auf der Basis von [Ti2W10PO40]7- und Chitosan
(2005)
The Keggin type polyoxotungstate [Ti2W10PO40]7- forms stable associates with the biopolymer chitosan in the nanometer size range. The cluster compound crystallizes from aqueous solution as K4H3[Ti2W10PO40] · 15H2O having a tetragonal structure. Both, the cluster compound and the chitosan/[Ti2W10PO40] associates show a high hydrolytic stability at pH 7.4. The associates formed between the cluster anion [Ti2W10PO40]7- with the polyaminosaccharide chitosan have been characterized by photon correlation spectroscopy, scanning electron microscopy, filtration, centrifugation and zeta potential measurements. The size of the associates formed is in the range of ca. 5×101 to 5×102 nm. These particles have a defined stoichiometry with 56 cluster anions bound per molecule chitosan. The isoelectric point determined by zeta potential measurements was found for a cluster anion to chitosan molar ratio of 5.5, indicating the charge neutralization between protonated chitosan and [Ti2W10PO40]7- anions. Cellular uptake studies with [Ti2W10PO40]7- using tumor cell lines FaDu (human squamous carcinoma) and HT-29 (human adenocarcinoma) showed that the tungsten amount inside the cells is remarkably enhanced in the presence of chitosan.
This paper presents the results of an interlaboratory study of the rheological properties of cement paste and ultrasound gel as reference substance. The goal was to quantify the comparability and reproducibility of measurements of the Bingham parameters yield stress and plastic viscosity when measured on one specific paste composition and one particular ultrasound gel in different laboratories using different rheometers and measurement geometries.
The procedures for both in preparing the cement paste and carrying out the rheological measurements on cement paste and ultrasound gel were carefully defined for all of the study’s participants. Different conversion schemes for comparing the results obtained with the different measurement setups are presented here and critically discussed. The procedure proposed in this paper ensured a reasonable comparability of the results with a coefficient of variation for the yield stress of 27% and for the plastic viscosity of 24%, despite the individual measurement series’ having been performed in different labs with different rheometers and measurement geometries.
"Ullmann's Encyclopedia of Industrial Chemistry" is the benchmark reference in chemistry and chemical and life science engineering, covering inorganic and organic chemicals, advanced materials, pharmaceuticals, polymers and plastics, metals and alloys, biotechnology and biotechnological products, food chemistry, process engineering and unit operations, analytical methods, environmental protection, and much more.
The present article is part of the topic collection "Environmental Protection and Industrial Safety". It covers plant and process safety, focusing on hazardous materials and process conditions.
Hexapotassium dihydrogen monotitanoundecatungstocobaltate(II) tridecahydrate, K6H2[TiW11CoO40]·13H2O, crystallizes from aqueous solution in the cubic space group P 3m. The structure was refined as an inversion twin. The [TiW11CoO40]8- anion has a Keggin structure with one W-atom site occupied by titanium and a central tetrahedral CoO4 group.
The CuII complex of H4TETP (H4TETP = 1,4,8,11-tetraazatetradecane-1,4,8,11-tetrapropionic acid) is five-coordinate with a distorted square-pyramidal structure (τ = 0.45; i.e. the geometry is nearly half-way between square-pyramidal and trigonal-bipyramidal) and a relatively long Cu–N and a short Cu–O bond; the comparison between powder and solution electronic spectroscopy, the frozen solution EPR spectrum and ligand-field-based calculations (angular overlap model, AOM) indicate that the solution and solid state structures are very similar, i.e. the complex has a relatively low 'in-plane' and a significant axial ligand field with a dx²-y² ground state. The ligand-enforced structure is therefore shown to lead to a partially quenched Jahn–Teller distortion and to a relatively low complex stability, lower than with the corresponding acetate-derived ligand H4TETA. This is confirmed by potentiometric titration and by the biodistribution with 64Cu-labeled ligands which show that the uptake in the liver is significantly increased with the H4TETP-based system.
Polyoxometalates (POMs) are inorganic cluster compounds that have been shown to possess a number of pharmacological properties, including antidiabetic, antibacterial, antiprotozoal, antiviral and anticancer activities. Their molecular mechanism of action is largely unknown. However, several studies indicate that many of their activities may be due to the inhibition of enzymes, in particular, of those enzymes that are accessible from the extracellular space and do not require the penetration of cell membranes. In this review, we describe the recent progress in the preparation and optimization of POMs, and an evaluation of their use as inhibitors of different families of enzymes. The next important steps in this area of research will be to gain a better understanding of the interactions of POMs with enzymes on a structural level through an X-ray crystallographic study of enzyme–POM complexes and the analysis of structure–activity relationships. Furthermore, POMs with increased stability and in vivo half-lives have to be prepared. Surface modification may allow the targeting of POM drugs at their sites of action.
Aspects of positional laser-GMA-hybrid welding using high alloyed tubular cored wire electrodes
(2008)
The phosphorylation of p-tert-butylcalix[8]arene (1) with phosphorus pentachloride and hydrolysis gives intramolecular bridging tert-butylcalix[8]arene triphosphates. The reactivity (esterification, dehydratisation, complexation), the structure (nmr and x-ray), and the stereochemical behaviour of the phosphates will be discussed.
The present study documents the results of an
inter-disciplinary model project that was planned with the
aim of developing an innovative winter covering system
for marble statuaries located on the Schlossbru¨cke (Berlin).
Such a system would need to fulfil the various requirements
for structural stability, aesthetics, climate and practical
use. This applied research represents the first complex
scientific study of the sustainability of a winter covering
system. The study is characterised by the use of complex
scientific instruments such as special laboratory analysis
and numerical simulation tools. The interaction between
the environment and the artefacts in connection with the
innovative winter covering structures were studied by
extensive climatic monitoring.
Laser-gas metal arc (GMA)-hybrid welding enables a high deposition rate and a stable welding process. Process stability was found to be profoundly dependent on the type of the applied filler wire (solid or tubular cored). Whereas solid wires are deposited in pulsed arc mode, tubular cored wire electrodes are weldable by a stable spray-arc process within a wide operating range. This fact applies above all to a high alloyed metal cored wire electrode, of which the achievable deposition rates exceed the upper limits recommended by the manufacturer. A further interesting aspect is the application of a rutile tubular cored wire for positional laser-GMA-hybrid welding. A modern 20 kW-fibre laser source was available for the experiments. This study is concerned with the weldability of high alloyed tubular cored electrodes for high power laser-GMA-hybrid welding. Results obtained from comparative investigations between tubular cored and solid wire electrodes relating to process stability are summarised.
Decay resistance of pine sapwood treated with titanium alkoxide solutions was tested against the brown-rot fungi Coniophora puteana and Poria placenta for exposure times of 10 and 16 wk. In practice, wood-specimens were vacuum-impregnated by alcoholic solutions of titanium alkoxide with concentrations in the range of 5–16 mass % (solid content in solution) and subsequently cured under different humidity conditions. Results reveal that treated wood degraded up to 5% in comparison to untreated one that deteriorated 38% and 50%, respectively against both wood-decay fungi. Even full protection (mass loss below 3%) was achieved against brown rot with titanium alkoxide solution containing solid content of around 5 mass% with a weight percentage gain (WPG) of 9 mass%. With increased concentration, fungal resistance decreased slightly which was associated with more cracks and imperfections formed in the deposited layers of titanium dioxide in the adjacent wood matrix. Thermal analysis verified that a considerable amount of precursor remained in the wood structure as un-hydrolyzed organic residues. These organics, being bioactive, had the tendency to induce similar fungicidal effects as those of conventional fungicides. The amount of organic residues is correlated with the decay resistance of the tested samples. In a prolonged decay test, mass losses of 16-wk incubated samples do not show behavior different from that of the wood samples incubated for 10 wk. This result implies that the decay protection is permanent and confirms further the fungicidal activity of titanium-alkoxide-treated wood.
The antileaching efficacy of sol-gel-derived TiO2- and SiO2-based precursors has been evaluated through laboratory leaching trials with pine sapwood in two different ways. In a one-step process, wood was vacuum impregnated by the precursor solutions containing CuCl2. The copper (Cu) emission rates of the sol-gel-based impregnated woods were up to 70% lower than that of wood treated with pure CuCl2 solution at the same level of concentration. More improvement (80%) could be achieved in a two-step process, in which sol-gel precursors were introduced into an already CuCl2-treated wood. The refinement was attributed to several effects. In the one-step approach, Cu was embedded in the TiO2/SiO2 gels formed in the wood texture. During a two-step impregnation, gel layers that were formed in the wooden interior acted as an effective diffusion barrier. The sol-gel impregnations made wood more hydrophobic; therefore, the low amount of water that penetrated the cell wall was less efficient to leach out Cu.
During the past 20 years, innovative developments in concrete technology have enabled the production of ultra-high performance fibre reinforced concretes (UHPFC) for the protection and preservation of concrete structures. The main characteristics of UHPFC comprise high compressive and flexural strength as well as high ductility compared to normal strength, normal weight concrete (NSC). This paper focuses on the analysis of crack formation and crack propagation in UHPFC under tensile loading under quasistatic conditions by using acoustic emission (AE) and optical deformation analysis (ODA).
AE is a non-destructive technique to monitor the development of micro structural damage processes caused by external forces. In this context, AE allows for a continuous monitoring of changes in the microstructure (cracks) over time and the corresponding localisation by appropriate algorithms. The AE measurements were performed along with ODA at the surface of the samples in order to analyse the deformation behaviour of the samples and the crack propagation.
For the tests, a UHPFC reference mixture was developed and tested with three different volume percentages of steel fibres (1.0 V.-%, 2.0 V.-%, and 3.0 V.-%). This paper shows that the application of AE is a suitable method to analyse the crack propagation in UHPFC specimens under tensile loading and to localise the crack initiation. Furthermore, insights into the failure mechanism of the fibres are offered by the analysis of the signals of the AE measurements, which allows for a better understanding of UHPFC and its general performance.
The preparation and characterization of tris-pyridyl bispidine (3,7-diazabicyclo[3.3.1]nonane) derivatives with benzimidazole and imidazole donor groups at the N-3 position of the bispidine Skeleton and their copper(II) complexes are reported. The impact of the hetaryl substituents on the configurational isomerism of piperidones and their corresponding bispidones has been studied by NMR spectroscopy, revealing the exclusive appearance in the enol form for the piperidones in solution and the trans-configuration regarding the two pyridyl substituents, as well as the sole formation of the unsymmetric exo-endo isomers for the corresponding bispidones. Thus, the bispidones are preorganized ligands for building pentacoordinated complexes, confirmed by the preparation and characterization of the corresponding Cu(II) complexes. Of the di-pyridyl piperidones with benzimidazole and imidazole substituents, and of the Cu(II) complex of the benzimidazole-containing bispidone, Crystals have become available for the analysis by X-ray diffraction, showing that the piperidones form the enol tautomers also in the solid state.
Bispidines for dual imaging
(2014)
The efficient transformation of the hexadentate bispidinol 1 into carbamate derivatives yields functional bispidines enabling convenient functionalization for targeted imaging. The BODIPY-substituted bispidine 3 combines a coordination site for metal ions, such as radioactive 64CuII, with a fluorescent unit. Product 3 was thoroughly characterized by standard analytical methods, single crystal X-ray diffraction, radiolabeling, and photophysical analysis. The luminescence of ligand 3 was found to be strongly dependent on metal ion coordination: CuII quenches the BODIPY fluorescence, whereas NiII and ZnII ions do not affect it. It follows that, in imaging applications with the positron emitter 64CuII, residues of its origin from enriched 64Ni and the decay products 64NiII and 64ZnII, efficiently restore the fluorescence of the ligand. This allows for monitoring of the emitted radiation as well as the fluorescence signal. The stability of the 64CuII–3 complex is investigated by transmetalation experiments with ZnII and NiII, using fluorescence and radioactivity detection, and the results confirm the high stability of 64CuII–3. In addition, metal complexes of ligand 3 with the lanthanide ions TbIII, EuIII, and NdIII are shown to exhibit emission of the BODIPY ligand and the lanthanide ion, thus enabling dual emission detection.
Four cyclam (1,4,8,11-tetraazacyclotetradecane) ligands with different numbers of N-substituted propionic acid groups lead to pentacoordinate copper(II) complexes that adopt trans-I configurations (4+1 geometry), that is, the complexes have a dx2-y2 ground state with significant rhombic distortion. From the structural data (X-ray diffraction analysis and electron paramagnetic resonance, UV/Vis and IR spectroscopy), as the number of secondary amine groups of the macrocyclic ring substituted with propionic acid groups increases, the distortion from square pyramidal to trigonal bipyramidal increases, and this is expected to lead to relatively low complex stabilities. This is confirmed by in vitro studies with superoxide dismutase (SOD) and human serum challenge experiments as well as by biodistribution data with the 64Cu-labelled complexes. The 64Cu-labelled complexes with cyclam monopropionic and dipropionic acid show high in vitro and in vivo stabilities, and the latter provides a comparable biodistribution profile to that of 64CuTETA (TETA = 1,4,8,11-tetraazacyclotetradecane-1,4,8,11-tetraacetic acid).
The paper descibes a novel method to detoxify pine wood (Pinus silvestris L.) treated with CCB-, CCF- CC-, and Cu-HDO-type salt preservatives. In the process of biological detoxification organic acids produced by strains of Antrodia vaillantii and other brown rot fungi are used for the dissolution of the previously fixed inorganic compounds. These findings are the basis for applying an acid pulping process (FORMACELL) developed by Nimz and Schone (1992) at the BFH, Hamburg, to detoxify salt impregnated wood waste with a mixture of acetic and formic acid. First results achieved with wood chips from treated poles after approximately 20 years of service life show that the obtained pulp contains less than 100 ppm of Cr and Cu. The pulp properties were neither influenced by the Cr and Cu ions nor by the age of the poles. The extracted quantities of Cr and Cu remain with the lignin whereas the acids are evaporated and recycled in the pulping process.
Composition and microstructure stability of cement compound under cyclic hydrothermal condition
(2020)
There have been many researches focused on the performance improvement of ultra-high performance concrete (UHPC) by autoclaving treatment. The goal of autoclaving is to increase the pozzolanic reaction, and to densify the cement stone and the transition zone which originates from the incorporation of supplementary cementitious materials (SCMs), such as silica fume, fly ash and blast furnace slag. Due to the superior properties, UHPC can also be utilized under high mechanical load and aggressive condition, for example, the fabrication of water tanks for thermal storage which is of great significance for saving energy and reducing CO2 emission. It is known that mineral stability of the hydration products of an inorganic binder is highly related to the temperature and pressure of the environment. A certain stable composition at room temperature, however, may undergo a phase transformation at high temperature and the performance decrease under this severe condition will generally be more severe. In this way, the rationale behind this deterioration under long-term hydrothermal condition involving many cycles and long duration has to be clarified, and then appropriate optimizing methods will be performed in order to obtain a kind of construction with high durability under aggressive environment. For this purpose, different types and amounts of SCMs are introduced into the standard mixture of UHPC and the phase compositions after autoclaving at 200 °C and 15.5 bar are determined by combined X-ray diffraction and scanning electron microscope. Mercury intrusion porosimeter is used to characterise the microstructure of the samples. In order to establish the relationship between microstructure and macroscopic properties, compressive and flexural strength are also investigated.
Chemischer Angriff auf Betonbauwerke - Bewertung des Angriffsgrads und geeignete Schutzprinzipien
(2014)
In verschiedenen Bereichen des Betonbaus ist Beton einem chemischen Angriff von außen ausgesetzt, der die Dauerhaftigkeit des betreffenden Bauteils bzw. des gesamten Bauwerks beeinträchtigen kann. Für einen chemischen Angriff in natürlichen Böden und Grundwässern bestehen normative Vorgaben in DIN 4030-1 [R10] bzw. DIN 1045-2 [R19], um den Angriffsgrad anhand der Art und Konzentration der angreifenden Stoffe in Expositionsklassen XA1 (schwach angreifend) bis XA3 (stark angreifend) einzustufen. Hinsichtlich weiterer maßgeblicher Einflussfaktoren wird an dieser Stelle nicht näher differenziert, ob und inwieweit die Regelungen für Böden und Grundwässer auch auf andere Bereiche mit chemischem Angriff auf Beton zu übertragen sind, ist stets im Einzelfall zu überprüfen. Ebenfalls sind die zu treffenden Maßnahmen über die Vorgaben der DIN EN 206-1/DIN 1045-2 [R19] hinaus anwendungsspezifisch festzulegen. Der Hauptausschuss Baustofftechnik (HABT) des DBV hat daher den Arbeitskreis "Chemischer Angriff auf Beton" beauftragt, dieses Merkblatt zu erarbeiten, das Hilfestellung bei der Bewertung einer projektspezifischen chemischen Angriffssituation auf Beton sowie bei der Planung und Ausführung von Schutzprinzipien leisten soll.
ln den letzten Jahren wurden diverse Prüfverfahren und Methoden entwickelt, um die Leistungsfähigkeit von Beton bzw. Bindemittel hinsichtlich des Widerstands gegenüber betonaggressiven Einwirkungen beurteilen zu können. Ein wesentliches Ziel von Prüfverfahren zur Beurteilung der Dauerhaftigkeit von Baustoffen ist, die im Laufe der Nutzungsdauer zu erwartenden Einwirkungen auf den Baustoff realitätsnah abzubilden. Dazu sind die Prüfparameter auf die im jeweiligen Anwendungsbereich vorherrschenden Umgebungs- und Randbedingungen anzupassen. Daneben sind auch die Bewertungskriterien individuell unter Berücksichtigung der im Einzelfall geforderten Nutzungsdauer eines Bauwerks festzulegen. Eine systematische Zuordnung von adäquaten Prüfverfahren bzw. Prüfparametem und Bewertungskriterien für die verschiedenen Anwendungsbereiche im Betonbau, in denen betonaggressive Einwirkungen auftreten, ist mit Ausnahme von Einzelfällen bislang nicht vorhanden. Daneben stellt sich in der Praxis immer wieder das Problem, das Angriffspotenzial der Umgebung eines Bauwerks (prüftechnisch) zu erfassen und zu bewerten.
Der Hauptausschuss Baustofftechnik des DBV hat daher den Arbeitskreis „Chemischer Angriff auf Beton“ beauftragt, dieses Merkblatt zu erarbeiten, das auf Basis von einschlägigen Erfahrungen der Baupraxis und wissenschaftlichen Erkenntnissen Grundsätze und bewährte Methoden zur Beurteilung der Einwirkungs- und Widerstandsseite beim chemischen Angriff auf Beton aufzeigt und diesbezüglich Hinweise für verschiedene Anwendungsbereiche im Betonbau liefert.
ABSTRACT: A collection of thioimidazolium salts were synthesized and used as a new class of nonvolatile alkylating agents. Their nonvolatility prevents exposure during use or handling and are thus drastically safer than conventional alkylating agents. We discovered that thioimidazolium Iodide salts cannot release volatile compounds in the solid state, but instead only decompose when molten. Since decomposition proceeds via alkyl iodide elimination, SN2 of iodide on the thioimidazolium cation is constrained in the solid state, and instead can occur only upon melting when ions are mobile. By smart design of these alkylators, the melting point and thus the decomposition temperature of these salts can be increased from 106 to 169 °C and release negligible volatile organic compounds prior to melting. Thioimidazolium-bis(trifluoromethanesulfonyl)imide (TFSI) ionic liquids act as a completely nonvolatile and air-stable TFSI-based alkylating agent and can be used for high-throughput Synthesis of TFSI ionic liquids without solvent. Alkyl groups from methyl to dodecyl can be transferred to a nucleophile and the product purified by sublimation of the thione byproduct, which can then be recycled. We also found that thioimidazolium salts with a dodecyl chain are bactericidal, yet can hydrolyze in water to form benign neutral products, and thus wont accumulate in the environment. These results demonstrate that thioimidazolium salts are a designable platform for the pursuit of safer and more environmentally friendly alkylating and antiseptic agents.
This article reports a comprehensive investigation of the average and local structure of La5.6WO12-δ, which has excellent mixed proton, electron and oxide ion conduction suitable for device applications. Synchrotron X-ray and neutron powder diffraction show that a cubic fluorite supercell describes the average structure, with highly disordered lanthanum and oxide positions. On average, the tungsten sites are sixfold coordinated and a trace [3.7 (1.3)%] of anti-site disorder is detected. In addition to sharp Bragg reflections, strong diffuse neutron scattering is observed, which hints at short-range order. Plausible local configurations are considered and it is shown that the defect chemistry implies a simple 'chemical exchange' interaction that favours ordered WO6 octahedra. The local model is confirmed by synchrotron X-ray pair distribution function analysis and EXAFS experiments performed at the La K and W L-3 edges. It is shown that ordered domains of similar to 3.5 nm are found, implying that mixed conduction in La5.6WO12-δ is associated with a defective glassy-like anion sublattice. The origins of this ground state are proposed to lie in the nonbipartite nature of the face-centred cubic lattice and the pairwise interactions which link the orientation of neighbouring octahedral WO6 sites. This 'function through frustration' could provide a means of designing new mixed conductors.