Analytische Chemie
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Besides their plasticizing effect, superplasticizers (SPs) are known to retard the hydration of inorganic systems such as cement. Despite their frequent use, the understanding of these highly complex systems is still limited and the relevant parameters, which control the interaction between SPs, and cement components and reaction products are in the focus of ongoing research activities.[1] Optical methods have been successfully used for the analysis and monitoring of the interactions between a broad variety of nanoscale and molecular systems like nanoparticles of various chemical composition and different types of organic ligands or biomolecules. The potential of these methods to study processes at the interface between (hydrated) particles and the fluid phase at a very early stage of concrete formation could reveal possible mechanisms of interaction.
This investigation focuses on the study of organic/inorganic mixtures consisting of cement (CEM) and cement phases (C3S and C3A) in the presence of polycarboxylate ether and organic dyes in aqueous solution (particularly alkali resistant dyes) at a water to powder ratio of 1. Diffuse reflectance as well as steady state and time resolved fluorescence spectroscopy of the above mentioned mixtures were evaluated. Based upon changes of the intensity of the reflectance and fluorescence signal and spectral changes of the dye, acting as optical reporter, a model for the interactions of dye, PCE and cement (including different cement phases) was derived which describes the very first stage of cement hydration.
The stimulated emission (SE) in aluminum laser-induced plasma pumped in resonance with the 3s23p − 3s24s aluminum transition at 266.04 nm is investigated experimentally. It is shown that the population Inversion between the 3s23p and 3s24s states can be created by weak pumping at several microjoule to millijoule pulse energies and result in high gain. The intensity of the SE at 396.15 nm is related to the number density of Al Atoms via absorption measurements. It is found that the SE in forward and backward directions with respect to the pumping laser is different in terms of the line shape and intensity that is attributed to inhomogeneity in a gain coefficient across the plasma plume.
The stimulated emission (SE) in aluminum laser-induced plasma pumped in resonance with the 3s²3p-3s²4s aluminum transition at 266.04 nm is modeled. A collisional-radiative plasma model based on kinetic equations is proposed to explain the creation of the population inversion and lasing. The model predicts fast depopulation of the ground 3s²3p state by the absorption of resonant laser light at 266 nm and very fast population of the excited 3s²4s state by the cascade transitions from the laser-pumped level, which is driven optically and by collisions. The SE of the 3s²3p-3s²4s transition at 396.15 nm is studied and possible SE at 1.3 and 2.1 μm is predicted. It is confirmed by calculations that the population inversion between the 3s²3p and 3s²4s states can be created by weak pumping at several microjoule–millijoule pulse energies and results in high gain.
We present the first spectroscopic study on a reverse glass painting form the classic modern period (1905-1955). Marianne Uhlenhuth’s painting “Ohne Titel, 1954” shows characteristics like experimental use of colorants and abstract compositions, which are well-established in classic modern art. Compared to stained glass, reverse glass paintings are viewed in reflected light, hence they reveal strong and intense colors. New inorganic pigments, development of synthetic organic pigments and the simultaneous supersession of well-known ancient colorants result in experimental works and remarkable pigment mixtures in this period of time. An in-situ, non-invasive approach was used to study the pigments and binding media. In-situ measurements were carried out using Raman spectroscopy (i-Raman®Plus, Bwtek Inc., 785 nm, 20× objective, resolution 4 cm-1), X-ray fluorescence (Tracer III-SD, Bruker AXS Microanalysis GmbH, 40 kV, 15 μA), VIS spectroscopy (SPM 100, Gretag-Imaging AG) and DRIFTS: Diffuse Reflection-Infrared-Fourier-Transform Spectroscopy (ExoScan, Agilent GmbH, 4000-650 cm-1, 256 scans, resolution 4cm-1). The pigments consist of inorganic as well as organic materials. Phthalocyanin green (PG7, colour index No. 74260), viridian and emerald green were used for the green areas. The yellow parts consist of chrome yellow and cadmium yellow. Pigment Yellow 1 (C.I. 11680) was used for the dark yellow/orange part. Red areas were characterized by the presence of cadmium and selenium (cadmium red) in the XRF spectrum. Ultramarine was detected in the blue parts. Concerning the violet color PR81 (bluish red, C.I. 45160:1) in mixture with PG7 (bluish green) were identified as main components. We want to outline that PR81 was rarely found in paintings. It was only recorded in the palettes of Lucio Fontana and Mary Cassatt before. The dark violet areas consist of Prussian blue and an unknown red (organic) colorant. Brown iron oxide was identified as the brown pigment. Bone black in mixture with black iron oxide were used as black materials and zinc white and titanium white as white pigments. XRF analysis of the metal color yields intense copper, zinc and nickel peaks (intensity ratio 3:3:1), which corresponds to “new silver” alloy. Barite and chalk are the fillers in this painting. Results of DRIFTS spectra show gum sometimes mixed with protein or oil (metal soaps) as binding media. The results point out that reverse glass paintings from the classic modern period are excellent examples to study the evolution of new pigments and their acceptance in artist’s palettes.
Multivariate data analysis is a universal tool for the evaluation of process spectroscopic data. In process analytics, huge amounts of information are produced i) by the many variables contained in one spectrum often exceeding 1000 (wavenumbers, wavelength, shifts…), and ii) the high number of spectra that is generated within the measurement period. Multivariate data analysis, often also called Chemometrics, help to extract the relevant information which is needed to examine and even control processes. Therefore, calibration models must be precise and robust, and moreover, must cover a wide range of variation of factors posing an influence on the process.
In this pre-conference course an introduction to both, explorative data analysis by PCA (Principal Component Analysis), and regression analysis by the most frequently used method, i.e. PLSR (Partial Least Squares Regression) is given. In principal, all optical spectroscopic methods are suited for multivariate evaluation. It will be demonstrated that under certain preconditions, even process NMR spectra can be predicted by PLSR models.
At first, basic principles of multivariate data analysis will be provided. This includes a short introduction into the concept of model building and interpretation of results. Detailed aspects of data pretreatment and calibration & validation strategies for chemometric models will be provided with own data from NIR, Raman and NMR spectroscopy.
In a first example, the development of an online compatible method for the quantification of methanol in biodiesel by PLSR is presented. This also includes the classification of biodiesel feedstocks by PCA and statistical tools which allow for the estimation of a full uncertainty budget.
The Raman spectroscopic prediction of Hydroformylation reaction in a miniplant is used to discuss shortcomings and pitfalls which may occur with the transfer of off-line models to the real processes. Design of experiment and strategies for suitable lab-scale experiments are presented as a possible way to overcome problems.
In a third application the prediction of the reactants of an esterification reaction based on process NMR data is demonstrated.
Contamination of natural bodies of water with oil and lubricants (or generally, hydrocarbon derivatives such as petrol, fuel and others) is a commonly found phenomenon around the world due to the extensive production, transfer and use of fossil fuels. The timely identification of these contaminants is of utmost importance, since they directly affect water quality and represent a risk for wildlife and human health even in trace amounts.
In this work, we develop a simple system for the on-field detection of total petroleum hydrocarbons (TPH) in water and soil, the "Spectrocube". The test is based on the measurement of the fluorescence signal emitted by the molecular rotor 4-DNS-OH dye. This dye is embedded in a hydrophobic polymeric matrix (PVDF), avoiding interactions of water with the dye and providing a robust support for use in test-strip fashion. The test-strip’s fluorescence intensity increases linearly at low concentrations of TPH, reaching a saturation value at higher concentrations.
For excitation and evaluation of the test-strip fluorescence, a simple miniature optical system was designed. The system works semi-quantitatively as solvent-free TPH detection kit, as well as quantitatively when using a simple cyclopentane extraction step. To simplify the fluorescence read-out, the device is coupled to a tablet computer via Bluetooth, running a self-programmed software ("app").
Aggregation-induced emission (AIE) has been meanwhile observed for many dye classes and particularly for fluorophores containing propeller-like groups. Herein, we report on the AIE characteristics of a series of four hydrophobic pyrrolidinylvinylquinoxaline (PVQ) derivatives with phenyl, pyrrolyl, indolyl, and methoxythienyl substituents used to systematically vary the torsion angle between this substituent at the quinoxaline C2 position and the planar PVQ moiety. These molecules, which are accessible via four- or five-component one-pot syntheses, were spectroscopically studied in organic solvents and solvent−water mixtures, as dye aggregates, solids, and entrapped in polystyrene particles (PSP). Steady-state and time-resolved fluorescence measurements revealed a strong fluorescence enhancement for all dyes in ethanol−water mixtures of high water content, accompanying the formation of dye aggregates with sizes of a few hundred nm, overcoming polarity and H-bonding-induced fluorescence quenching of the chargetransfer-type emission of these PVQ dyes. The size and shape of these dye aggregates and the size of the AIE effect are controlled by the water content and the substituent-dependent torsion angle that influences the nucleation process and the packing of the molecules during aggregation. Staining of 1 μm-sized carboxy-functionalized PSP with the PVQ dyes resulted also in a considerable increase in the fluorescence quantum yield and lifetime, reflecting the combined influence of the restricted molecular motion and the reduced polarity of the dye microenvironment.
The technique of painting on the reverse side of a glass panel was rediscovered by German artists at the beginning of the 20th century. They appreciated the impressive gloss, luminosity, and depth of colours in this genre. Compared to stained glass, the distinctive properties of this technique are: (1) the paint is applied “cold”, hence, it doesn’t involve a firing step, (2) reverse paintings on glass are framed and always viewed in reflected light and (3) the reverse paint stratigraphy is different from canvas paintings, starting with the front most layer and ending with the backing layer. In 1908 several artists, including Gabriele Münter, Wassily Kandinsky, Heinrich Campendonk, August Macke and Franz Marc of the “Der Blaue Reiter” (the Blue Rider) collective took an interest in this technique and started to share their interest with other colleagues in Europe. Our pioneering project is tracing this transfer of knowledge by a multidisciplinary approach in terms of art history, paint technology and material science. More than 100 artists and >1000 reverse paintings on glass were identified during the project. This high number of objects clearly points out that this technique was by far more important for modern art than previously assumed. In-situ, non-invasive measurements (XRF, Raman, VIS, DRIFTS) on a well-considered selection of 67 paintings reveal the broad palette of colorants ranging from traditional to experimental. Special attention is paid to the impact of synthetic organic pigments (SOP) in artists palette. Demonstrative examples by W. Kandinsky, L. G. Buchheim and F. Jespers are used to discuss analytical challenges and highlights.
A wide range of methods are used to estimate the plant-availability of soil phosphorus (P). Published research has shown that the diffusive gradients in thin films (DGT) technique has a superior correlation to plant-available P in soils compared to standard chemical extraction tests. In order to identify the plant-available soil P species, we combined DGT with infrared and P K- and L-edge X-ray adsorption near-edge structure (XANES) spectroscopy. This was achieved by spectroscopically investigating the dried binding layer of DGT devices after soil deployment. All three spectroscopic methods were able to distinguish between different kinds of phosphates (poly-, trimeta-, pyro- and orthophosphate) on the DGT binding layer. However, infrared spectroscopy was most sensitive to distinguish between different types of adsorbed inorganic and organic phosphates. Additionally, also intermediates of the time-resolved hydrolysis of trimetaphosphate in soil could be analyzed. Furthermore, infrared and XANES microspectroscopy make it also possible to analyze P compounds on the binding layer with a lateral resolution down to 1 µm2. Therefore, P species of a spatial soil segment (e.g. rhizosphere) can be mapped and analyzed.
The characterization of a catalyst often occurs by averaging over large areas of the catalyst material. On the other hand, optical probing is easily achieved at a resolution at the micrometer scale, specifically in microspectroscopy. Here, using surface-enhanced Raman scattering (SERS) mapping of larger areas with micrometer-sized spots that contain tens to hundreds of supported gold nanoparticles each, the photoinduced dimerization of p-aminothiophenol (PATP) to 4,4′-dimercaptoazobenzene (DMAB) was monitored. The mapping data reveal an inhomogeneous distribution of catalytic activity in the plasmon-catalyzed reaction in spite of a very homogeneous plasmonic enhancement of the optical signals in SERS. The results lead to the conclusion that only a fraction of the nanostructures may be responsible for a high catalytic activity. The high spot-to-spot variation in catalytic activity is also demonstrated for DMAB formation by the plasmon-catalyzed reduction from p-nitrothiophenol (PNTP) and confirms that an improvement of the accuracy and reproducibility in the characterization of catalytic reactions can be achieved by microspectroscopic probing of many positions. Using SERS micromapping during the incubation of PATP, we demonstrate that the reaction occurs during the incubation process and is influenced by different parameters, leading to the conclusion of dimerization in a gold-catalyzed, nonphotochemical reaction as an alternative to the plasmon-catalyzed process. The results have implications for the future characterization of new catalyst materials as well as for optical sensing using plasmonic materials.