Analytische Chemie
Filtern
Erscheinungsjahr
- 2022 (615) (entfernen)
Dokumenttyp
- Vortrag (217)
- Zeitschriftenartikel (191)
- Posterpräsentation (89)
- Beitrag zu einem Tagungsband (59)
- Forschungsbericht (17)
- Sonstiges (14)
- Forschungsdatensatz (10)
- Buchkapitel (7)
- Dissertation (2)
- Handbuch (2)
Sprache
- Englisch (529)
- Deutsch (85)
- Mehrsprachig (1)
Schlagworte
- Fluorescence (24)
- Digitalization (22)
- Certification (20)
- Conformity assessment (20)
- COVID-19 (19)
- Digital transformation (19)
- Sensor (19)
- Calibration (18)
- Conformity assessment body (18)
- Quality infrastructure (18)
Organisationseinheit der BAM
- 8 Zerstörungsfreie Prüfung (235)
- 1 Analytische Chemie; Referenzmaterialien (215)
- 6 Materialchemie (111)
- 8.2 Zerstörungsfreie Prüfmethoden für das Bauwesen (54)
- 8.4 Akustische und elektromagnetische Verfahren (53)
- 8.0 Abteilungsleitung und andere (52)
- 1.1 Anorganische Spurenanalytik (44)
- 8.5 Röntgenbildgebung (44)
- 6.1 Oberflächen- und Dünnschichtanalyse (42)
- 1.2 Biophotonik (40)
- 6.3 Strukturanalytik (40)
- 1.8 Umweltanalytik (35)
- S Qualitätsinfrastruktur (32)
- 8.1 Sensorik, mess- und prüftechnische Verfahren (31)
- S.2 Digitalisierung der Qualitätsinfrastruktur (30)
- 1.3 Instrumentelle Analytik (28)
- 4 Material und Umwelt (27)
- 1.4 Prozessanalytik (26)
- 1.9 Chemische und optische Sensorik (21)
- 8.6 Faseroptische Sensorik (20)
- 1.7 Organische Spuren- und Lebensmittelanalytik (19)
- 6.6 Physik und chemische Analytik der Polymere (19)
- 1.5 Proteinanalytik (18)
- 1.6 Anorganische Referenzmaterialien (16)
- VP Vizepräsident (16)
- VP.1 eScience (16)
- 6.5 Synthese und Streuverfahren nanostrukturierter Materialien (15)
- 6.0 Abteilungsleitung und andere (14)
- 4.3 Schadstofftransfer und Umwelttechnologien (10)
- 4.2 Material-Mikrobiom Wechselwirkungen (9)
- 7 Bauwerkssicherheit (9)
- 9 Komponentensicherheit (9)
- 3 Gefahrgutumschließungen; Energiespeicher (7)
- 4.5 Kunst- und Kulturgutanalyse (6)
- 5 Werkstofftechnik (5)
- 3.1 Sicherheit von Gefahrgutverpackungen und Batterien (4)
- 9.0 Abteilungsleitung und andere (4)
- 5.1 Mikrostruktur Design und Degradation (3)
- 6.2 Material- und Oberflächentechnologien (3)
- 7.4 Baustofftechnologie (3)
- 7.6 Korrosion und Korrosionsschutz (3)
- 9.5 Tribologie und Verschleißschutz (3)
- 1.0 Abteilungsleitung und andere (2)
- 2 Prozess- und Anlagensicherheit (2)
- 3.5 Sicherheit von Gasspeichern (2)
- 4.1 Biologische Materialschädigung und Referenzorganismen (2)
- 4.4 Thermochemische Reststoffbehandlung und Wertstoffrückgewinnung (2)
- 5.4 Multimateriale Fertigungsprozesse (2)
- 9.4 Integrität von Schweißverbindungen (2)
- P Präsident (2)
- P.0 Präsident und andere (2)
- S.1 Qualität im Prüfwesen (2)
- 2.1 Sicherheit von Energieträgern (1)
- 2.5 Konformitätsbewertung Explosivstoffe/Pyrotechnik (1)
- 3.2 Gefahrguttanks und Unfallmechanik (1)
- 5.2 Metallische Hochtemperaturwerkstoffe (1)
- 6.7 Materialsynthese und Design (1)
- 7.1 Baustoffe (1)
- 7.3 Brandingenieurwesen (1)
- 7.5 Technische Eigenschaften von Polymerwerkstoffen (1)
- 7.7 Modellierung und Simulation (1)
- 9.2 Versuchsanlagen und Prüftechnik (1)
- 9.6 Additive Fertigung metallischer Komponenten (1)
- VP.2 Informationstechnik (1)
Paper des Monats
- ja (5)
This contribution presents a set of largely novel reference standards specially designed for testing different important physical effects and functionalities of radiography-based computed tomography (CT) simulation software. These standards were developed within the scope of the German cooperation project “CTSimU – Radiographic Computed Tomography Simulation for Measurement Uncertainty Evaluation” [1] and serve as tools for the basic qualification of the sufficient physical correctness and required features of simulation software of CT-based coordinate measurement systems (CMSs) via the analyses either of 2D projection images only or of full CT scans. The results serve as input to the German standardisation committee for the development of a new national VDI/VDE guideline in the series VDI/VDE 2630 dealing with the basic qualification aspect of CT simulation software and shall lay ground for the measurement uncertainty determination of dimensional measurements using CT.
An important focus of research in Industrial X-ray Computed Tomography (CT) is to determine the task-specific measurement uncertainty of CT measurements numerically by using simulations. For this, all relevant influence factors need to be identified and quantified. It is known, for example, that geometrical misalignments of the detector lead to measurement deviations if the reconstruction does not consider these misalignments. This contribution uses computer simulation of CT data to investigate the influence of geometrical misalignments of the detector on several measurands found in typical measurements tasks in the industry. A newly developed test specimen with a broad variety of features is used for this study. Angular and positional detector deviations are systematically introduced into the simulations and deliberately left uncompensated during the CT reconstruction. The resulting measurement deviations are shown and discussed.
The study, dedicated to Beautiful Pietàs conserved in South Tyrol (Northern Italy), aims to establish, for the first time, a connection between Austroalpine raw materials and the high-fired gypsum mortars constituting the Gothic figure groups in question. The origin and chronology of this stylistically and qualitatively differing ensemble have been subject of art historical debate for nearly a century. The discourse is dominated by three main hypotheses: itinerary of an Austrian artist versus itinerary of the work of art created in an artist’s workshop in Austria versus itinerary of the stylistic vocabulary via graphical or three-dimensional models. The comparison of the δ34S values and the 87Sr/86Sr ratios of the gypsum mortars and Austroalpine sulphate deposits (in a compilation of own reference samples and literature data) points to the exploitation of sediments in the Salzkammergut and possibly also in the evaporite district of the Eastern Calcareous Alps, thus evidencing the import of the sculptures and not the activities of local South Tyrolean or itinerant artists. Two geochronological units are distinguishable: The Pietà in the Church St. Martin in Göflan can be assigned to Upper Permian raw material, whereas the metrologically consistent sculptures in the Church of Our Lady of the Benedictine Abbey Marienberg and in the Chapel St. Ann in Mölten correlate with deposits of the Early Triassic (or the Lower-Middle Triassic transition). The medieval gypsum mortars also differ in their mineralogical characteristics, i.e. in their geologically related minor components, as in the first case, characterised by a significant proportion of primary anhydrite, natural carbonate impurities mainly consist of calcite (partly converted to lime-lump-like aggregates), whereas in the second group dolomite (or rather its hydration products after pyrometamorphic decomposition) predominates, accompanied by celestine, quartz and potassium feldspar. The Pietà in the Cathedral Maria Himmelfahrt in Bozen turned out to be made of Breitenbrunn calcareous sandstone (Leitha Mountains, Burgenland, Austria), which is why the sample is not considered in the geochemical analysis.
Light-emitting nanoparticles like semiconductor nanocrystals (termed quantum dots, QDs) are promising candidates for biosensing and bioimaging applications based on their bright and stable photoluminescent properties. As high-quality QDs are often synthesized in organic solvents, strategies needed to be developed to render them water-dispersible without affecting their optical properties and prevent changes in postmodification steps like the biofunctionalization with antibodies or DNA. Despite a large number of studies on suitable surface modification procedures, the preparation of water-soluble QDs for nanobiotechnology applications still presents a challenge. To highlight the advantages of surface silanization, we systematically explored the influence of the core/multishell architecture of CdSe/CdS/ZnS QDs and the silanization conditions on the optical properties of the resulting silanized QDs. Our results show that the optical properties of silica-coated CdSe/CdS/ZnS QDs are best preserved in the presence of a thick CdS (6 monolayers (ML)) intermediate shell, providing a high photoluminescence quantum yield (PL QY), and a relatively thick ZnS (4.5 ML) external shell, effectively shielding the QDs from the chemical changes during silica coating. In addition to the QD core/shell architecture, other critical parameters of the silica-coating process, that can have an influence on the optical properties of the QD, include the choice of the surfactant and its concentration used for silica coating. The highest PL QY of about 46% was obtained by a microemulsion silica-coating procedure with the surfactant Brij L4, making these water-dispersible QDs to wellsuited optical reporters in future applications like fluorescence immunoassays, biomedicine, and bioimaging.
Protein immobilization for the functionalization of particles is used in various applications, including biosensors, lateral-flow immunoassays (LFIA), bead-based assays, and others. Common methods for the quantification of bound protein are measuring protein in the supernatant before and after coating and calculating the difference. This popular approach has the potential for a significant overestimation of the amount of immobilized protein since layers not directly bound to the surface (soft protein corona) are usually lost during washing and handling. Only the layer directly bound to the surface (hard corona) can be used in subsequent assays. A simplified amino acid analysis method based on acidic hydrolysis and RP-HPLC-FLD of tyrosine and phenylalanine (aromatic amino acid analysis, AAAA) is proposed to directly quantify protein bound to the surface of gold nano- and latex microparticles. The results are compared with indirect methods such as colorimetric protein assays, such as Bradford, bicinchoninic acid (BCA), as well as AAAA of the supernatant. For both particle types, these indirect quantification techniques show a protein overestimation of up to 1700% compared to the direct AAAA measurements. In addition, protein coating on latex particles was performed both passively through adsorption and covalently through EDC/sulfo-NHS chemistry. Our results showed no difference between the immobilization methodologies. This finding suggests that usual protein determination methods are no unambiguous proof of a covalent conjugation on particles or beads.
The fourth dataset dedicated to the Open Guided Waves platform presented in this work aims at a carbon fiber composite plate with an additional omega stringer at constant temperature conditions. The dataset provides full ultrasonic guided wavefields. Two types of signals were used for guided wave excitation, namely chirp signal and tone-burst signal. The chirp signal had a frequency range of 20-500kHz. The tone-burst signals had a form of sine modulated by Hann window with 5 cycles and carrier frequencies 16.5kHz, 50kHz, 100kHz, 200kHz, 300kHz. The piezoceramic actuator used for this purpose was attached to the center of the stringer side surface of the core plate. Three scenarios are provided with this setup: (1) wavefield measurements without damage, (2) wavefield measurements with a local stringer debond and (3) wavefield measurements with a large stringer debond. The defects were caused by impacts performed from the backside of the plate. As result, the stringer feet debonds locally which was verified with conventional ultrasound measurements.
MALDI-TOF-MS-based identification of monoclonal murine anti-SARS-CoV-2 antibodies within one hour
(2022)
During the SARS-CoV-2 pandemic, many virus-binding monoclonal antibodies have been developed for clinical and diagnostic purposes. This underlines the importance of antibodies as universal bioanalytical reagents. However, little attention is given to the reproducibility crisis that scientific studies are still facing to date. In a recent study, not even half of all research antibodies mentioned in publications could be identified at all. This should spark more efforts in the search for practical solutions for the traceability of antibodies. For this purpose, we used thirty-five monoclonal antibodies against SARS-CoV-2 to demonstrate how sequence-independent antibody identification can be achieved by simple means applied onto the protein. First, we examined the intact and light chain masses of the antibodies relative to the reference material NIST-mAb 8671. Already half of the antibodies could be identified based solely on these two parameters. In addition, we developed two complementary peptide mass fingerprinting methods with MALDI-TOF-MS that can be performed in 45 minutes and had a combined sequence coverage of over 80%. One method is based on the partial acidic hydrolysis of the protein by 5 mM of sulfuric acid at 99 °C. Furthermore, we established a fast way for a tryptic digest without an alkylation step. We were able to show that the distinction of clones is possible simply by a brief visual comparison of the mass spectra. In this work, two clones originating from the same immunization gave the same fingerprints. Later, a hybridoma sequencing confirmed the sequence identity of these sister clones. In order to automate the spectral comparison for larger libraries of antibodies, we developed the online software ABID 2.0 (https://gets.shinyapps.io/ABID/). This open-source software determines the number of matching peptides in the fingerprint spectra. We propose that publications and other documents critically relying on monoclonal antibodies with unknown amino acid sequences should include at least one antibody fingerprint. By fingerprinting an antibody in question, its identity can be confirmed by comparison with a library spectrum at any time and context.
The fabrication of nanostructures with ever-decreasing sizes has increased the demand of suitable characterization methods which allow to determine their shape and size at the true nanoscale, and similarly important, enable the investigation of their optical properties beyond the diffraction limit. Due to its high spectral and spatial resolution down to the (sub-) nanometer range, electron beam-based techniques, namely cathodoluminescence (CL) has become a powerful characterization tool, particularly to study plasmonic and dielectric nanostructures. However, the interpretation of the resulting spectral CL maps is not always unambiguously straightforward.
In this work, Mie resonances in single Si nanospheres of different sizes have been systematically studied, using experimental CL spectroscopy and an analytical CL model. For smaller spheres (r ~ 75 nm), the eigenmodes can be unequivocally identified, with relative changes in intensity of the electric and magnetic dipole depending on the electron beam position within the sphere. However, in larger spheres (r ~ 105 nm), the modal assignment becomes increasingly difficult due to a larger number of Mie modes in the visible spectral range. Additionally, penetrating electron beams generate two radiating dipoles at the two Si interfaces – due to the electron and its image charge collapsing at those interfaces – which can, depending on the electron beam’s velocity and its path length inside the particle, produce distinct resonances or dips (constructive or destructive interference of those two radiative dipoles). It is demonstrated that superimposed on the eigenmodes of the studied nanospheres, these resonances can distort the recorded spectrum and lead to potentially erroneous assignment of modal characters to the spectral features. An intuitive analogy is developed to unambiguously distinguish those resonance induced by transition radiation from the nanoparticle-specific Mie resonances.
Dieses Dokument fasst den Projekfortschritt des BAM-Projektes "Entwicklung von Wärmenachbehandlungsstrategien zur Vermeidung von Spannungsrelaxationsrissen" im Rahmen des Fachausschusses 1 "Schweißmetallurgie" des DVS e.V. für das Projektjahr 2021 zusammen und stellt die wichtigsten Ergebnisse in Kurzform vor.
This paper presents first advances in the area of aerial chemical trail following. For that purpose, we equipped a palm-size aerial robot, based on the Crazyflie 2.0 quadrocopter, with a small lightweight metal oxide gas sensor for measuring evaporated ethanol from chemical trails. To detect and localize a 5 cm wide chemical trail, a detection criterion was developed that uses only relative changes in the transient phase of the sensor response. The reduction in signal strength dependence improves the robustness of its application. We tested our setup in first crossing-trail experiments showing that our flying ant robot can correlate an odor hit with the chemical trail within 0.14 m. Principally, this could enable aerial chemical trail following in the future.
In der Masterarbeit wurde ein Screening gegen den CCMV mit einer linearen Peptidbibliothek entwickelt, wobei zwei lineare Binder identifiziert wurden. Das resynthetisierte Peptid wurde auf seine Bindungseigenschaften mittels ELISA und MST untersucht. Aufgrund eines Aminosäurefehlers in der selbst durchgeführten Resynthese des Peptids sind die Ergebnisse nicht vollständig übertragbar. Um eine umsetzbare Cyclusgröße für die Peptidbibliothek zu finden, wurden Ringgrößen mit sechs bis acht Aminosäuren untersucht. Da keiner der gewählten Ringgrößen bevorzugt war, wurde die Ringgröße aus acht Aminosäuren für die Peptidbibliothek gewählt. Der Ringschluss wurde durch die Bildung einer Disulfidbrücke erreicht. Dadurch war die Alkylierung der vorhandenen Thiolgruppe in den Abbruchsequenzen notwendig.
Neben den etablierten Alkylierungsreagenzien Iodessigsäure, Iodacetamid und Acrylamid wurden zwei Epoxide mituntersucht. Hierbei konnte nur bei Acrylamid und Propylenoxid eine vollständige Alkylierung beobachtet werden. Eine synthetische Peptidbibliothek aus zehn Aminosäuren pro Kopplungsschritt und einer Peptidlänge von acht Aminosäuren wurde erfolgreich nach der Split-and-Mix-Synthese hergestellt. Neben den kanonischen Aminosäuren wurde die synthetische Aminosäure 3-(3-Pyridyl)-alanin in die Peptidbibliothek mit eingebaut. Peptidsequenzen aus der cyclische Peptidbibliothek konnte mittels MALDI-TOF-MS identifiziert werden. Es konnte außerdem gezeigt werden, dass synthetische Aminosäuren mit proteinogenen Aminosäuren erfolgreich übersetzt werden. Anschließend wurde das entwickelte Screening auf eine cyclische Peptidbibliothek übertragen. Dabei konnte kein Binder identifiziert werden, da zu viele Nebenreaktionen auftraten. Ein alternativer Ringschluss über die Seitenketten von Lysin und Cystein wurden mit ortho-Phthaldialdehyd und 2,4,6-Trichloro-1,3,5-triazin (Cyanurchlorid) untersucht. Beide Bedingungen wiesen keinen erfolgreichen Ringschluss auf. Obwohl der Ringschluss über die Seitenketten von Lysin und Cystein nicht erfolgreich war, sollte ein Austausch von Cystein angestrebt werden, so dass kein freies Cystein in den Abbruchsequenzen vorhanden ist und die Alkylierung überflüssig wäre. Der Ringschluss durch Verwendung anderer Seitenketten bietet einen vielseitigen Ansatz.
Bifunctional fluorescent molecular oxoanion probes based on the benzoxadiazole (BD) chromophore are described which integrate a thiourea binding motif and a polymerizable 2-aminoethyl methacrylate unit in the 4,7-positions of the BD core. Concerted charge transfer in this electron donor-acceptor-donor architecture endows the dyes with strongly Stokes shifted (up to >250 nm) absorption and fluorescence. Binding of electron-rich carboxylate guests at the thiourea receptor leads to further analyte-induced red-shifts of the emission, shifting the fluorescence maximum of the complexes to ≥700 nm. Association constants for acetate are ranging from 1–5×105 M−1 in acetonitrile. Integration of one of the fluorescent probes through its polymerizable moiety into molecularly imprinted polymers (MIPs) grafted from the surface of submicron silica cores yielded fluorescent MIP-coated particle probes for the selective detection of antibiotics containing aliphatic carboxylate groups such as enoxacin (ENOX) at micromolar concentrations in highly polar solvents like acetonitrile.
In current Li-ion batteries electrode materials consist typically of inorganic materials, such as LiCoO2, LiNixCoyMn1-zO2, LiFePO4, Li4Ti5O12. These materials struggle with toxicity or limited mineral resources, making them expensive. Therefore, eco-friendly, sustainable, and low-cost alternatives are researched for in recent years. A series of organic compounds were investigated as electrode materials for alkali-ion batteries. Among them organic carbonyl-based materials show reversible storage of lithium- or sodium-ions. Metal terephthalates stand out with their easy synthesis, moderate operational voltage and enhanced dissolution stability compared to other organic compounds. One degradation pathway consists of the dissolution of the electrode material by HF, formed in a side reaction by water and the fluorous electrolyte. Fluorinated metal terephthalates could offer higher dissolution stability against HF and less contamination by water due to their increased hydrophobicity.
The goal of this project is the synthesis and the investigation of the formation mechanism of a series of calcium-based MOFs with increasing fluorine content. For this purpose, we aimed for the construction of calcium-based MOFs with terephthalic acid (H2-pBDC), 2-fluoro-terephthalic acid (H2-2F-pBDC), 2,3,4,5-tetrafluoroterephthalic acid (H2-pBDC-F4), isophthalic acid (H2-mBDC) and 5-fluoro-isophthalic acid (H2-5F-mBDC).
Traceable determination of non-static XCT machine geometry: New developments and case studies
(2022)
It is fundamental to determine the machine geometry accurately for dimensional X-ray computed tomography (XCT) measurements. When performing high-accuracy scans, compensation of a non-static geometry, e.g. due to rotary axis errors or drift, might become necessary. Here we provide an overview of methods to determine and account for such deviations on a per projection basis. They include characterisation of stage error motions, in situ geometry measurements, numerical simulations, and reconstruction-based optimization relying on image quality metrics and will be discussed in terms of their metrological performance. Since a radiographic calibration is always required to provide an initial absolute geometry, this method will be presented as well. The improvements of the XCT geometry correction methods are presented by means of case studies. The methods can be applied individually or in combination and are intended to provide a toolbox for XCT geometry compensation.
A software toolbox is introduced that addresses several needs common to computed tomography (CT). Built for the WIPANO CTSimU project to serve as the reference implementation for its image processing and evaluation tasks, it provides a Python 3 interface that is adaptable to many conceivable applications. Foremost, the toolbox features a pipeline architecture for sequential 2D image processing tasks, such as flat field corrections and image binning, and enables the user to create their own processing modules. Beyond that, it provides means to measure line profiles and image quality assessment algorithms to calculate modulation transfer functions (MTF) or to determine the interpolated basic spatial resolution (iSRb) using a duplex wire image. It can also be used to calculate projection matrices for the reconstruction of scans with arbitrary industrial CT geometries and trajectories. The CTSimU project defined a framework of projection- and volume-based test scenarios for the qualification of radiographic simulation software towards its use in dimensional metrology. The toolbox implements the necessary evaluation routines and generates reports for all projection-based tests.
Development of an Accurate and Robust Air-Coupled Ultrasonic Time-of-Flight Measurement Technique
(2022)
Ultrasonic time-of-flight (ToF) measurements enable the non-destructive characterization of material parameters as well as the reconstruction of scatterers inside a specimen. The time-consuming and potentially damaging procedure of applying a liquid couplant between specimen and transducer can be avoided by using air-coupled ultrasound. However, to obtain accurate ToF results, the waveform and travel time of the acoustic signal through the air, which are influenced by the ambient conditions, need to be considered. The placement of microphones as signal receivers is restricted to locations where they do not affect the sound field. This study presents a novel method for in-air ranging and ToF determination that is non-invasive and robust to changing ambient conditions or waveform variations. The in-air travel time was determined by utilizing the azimuthal directivity of a laser Doppler vibrometer operated in refracto-vibrometry (RV) mode. The time of entry of the acoustic signal was determined using the autocorrelation of the RV signal. The same signal was further used as a reference for determining the ToF through the specimen in transmission mode via cross-correlation. The derived signal processing procedure was verified in experiments on a polyamide specimen. Here, a ranging accuracy of <0.1 mm and a transmission ToF accuracy of 0.3μs were achieved. Thus, the proposed method enables fast and accurate non-invasive ToF measurements that do not require knowledge about transducer characteristics or ambient conditions.
Mit dem zerstörungsfreien Verfahren der nuklear magnetischen Resonanz (NMR) mit Fokus auf 1H-Protonen lässt sich der Feuchtegehalt in porösen Materialien bestimmen und bei einem vollgesättigten Medium eine Porengrößenverteilung ableiten. Für die Ermittlung der Porengrößenverteilung muss die gemessene T2-Relaxationszeitenverteilung mit dem Parameter Oberflächenrelaxivität (OR) umgerechnet werden. Ist dieser Parameter für das zu untersuchende Medium unbekannt, kann dieser mithilfe von Vergleichsverfahren abgeschätzt werden. Dabei kommen z. B. Gassorption, Quecksilberporosimetrie (MIP), Dünnschliff-Mikroskopie oder µ-Computer-Tomographie (µ-CT) zum Einsatz. Da die verschiedenen Verfahren allerdings unterschiedliche Auflösungsgrenzen aufweisen und auf verschiedenen physikalischen Prinzipien beruhen, können die ermittelten ORs für ein Medium stark variieren. Um ein besseres Verständnis für die OR und die Einflüsse der Vergleichsverfahren zu bekommen, wurden 19 verschiedene Sandsteintypen untersucht. Die OR wurde zum einen basierend auf der spezifischen inneren Oberfläche aus der dynamischen Dampfsorption (DVS) und der Gassorption abgeleitet. Zum anderen wurden die Relaxationszeitenverteilungen durch manuelles Anpassen der OR derart in Porengrößenverteilungen umgerechnet, sodass es eine Übereinstimmung mit den Porengrößenverteilungen aus MIP und/oder µ-CT gibt. Die Umrechnung von Relaxationszeitverteilungen in eine Porengrößenverteilung berücksichtigt dabei sowohl fast- als auch slow-diffusion. Insgesamt ergab sich für die Sandsteine ein breites Spektrum an ORs, bei dem die über die innere spezifische Oberfläche ermittelten ORs andere Größenordnungen aufwiesen (< 10 µm/s), als bei dem Vergleich mit MIP oder µ-CT (bis 600 µm/s). Die mit MIP und µ-CT ermittelten Werten lagen dabei um einen Faktor von 1 bis 30 auseinander. Dieser umfangreiche Datensatz, der vier verschiedene Vergleichsverfahren einbezieht, soll neue Erkenntnisse in der Charakterisierung von porösen Materialien (z. B. bezüglich der Oberflächenrauigkeit) und in der Ursache für die starke Variation der OR ermöglichen. Durch das Berücksichtigen von fast- als auch slow-diffusion, können dabei sogar Daten in eine Porengrößenverteilung umgerechnet werden, bei denen das fast-diffusion-Kriterium nach Brownstein und Tarr nicht erfüllt ist. Außerdem ergibt sich aus der Berücksichtigung des slow-diffusion-Regimes ein neues Verständnis für die obere Auflösungsgrenze von NMR.
Stability, dissolution, and cytotoxicity of NaYF4‑upconversion nanoparticles with different coatings
(2022)
Upconversion nanoparticles (UCNPs) have attracted considerable attention owing to their unique photophysical properties. Their utilization in biomedical applications depends on the understanding of their transformations under physiological conditions and their potential toxicity. In this study, NaYF4: Yb,Er UCNPs, widely used for luminescence and photophysical studies, were modified with a set of four different coordinatively bound surface ligands, i.e., citrate, alendronate (AA), ethylendiamine tetra(methylene phosphonate) (EDTMP), and poly(maleic anhydride-alt-1-octadecene) (PMAO), as well as silica coatings with two different thicknesses. Subsequently, the aging-induced release of fluoride ions in water and cell culture media and their cytotoxic profile to human keratinocytes were assessed in parallel to the cytotoxic evaluation of the ligands, sodium fluoride and the lanthanide ions. The cytotoxicity studies of UCNPs with different surface modifications demonstrated the good biocompatibility of EDTMP-UCNPs and PMAO-UCNPs, which is in line with the low amount of fluoride ions released from these samples. An efficient prevention of UCNP dissolution and release of cytotoxic ions, as well as low cytotoxicity was also observed for UCNPs with a sufficiently thick silica shell. Overall, our results provide new insights into the
understanding of the contribution of surface chemistry to the stability, dissolution behavior, and cytotoxicity of UCNPs. Altogether, the results obtained are highly important for future applications of UCNPs in the life sciences and bioimaging studies.
The development of methodologies to sense glyphosate has gained momentum due to its toxicological and ecotoxicological effects. In this work, a red-emitting and polymerizable guanidinium benzoxadiazole probe was developed for the fluorescence detection of glyphosate. The interaction of the fluorescent probe and the tetrabutylammonium salt of glyphosate was studied via UV/vis absorption and fluorescence spectroscopy in chloroform and acetonitrile. The selective recognition of glyphosate was achieved by preparing molecularly imprinted polymers, able to discriminate against other common herbicides such as 2,4-dichlorophenoxyacetic acid (2,4-D) and 3,6-dichloro-2-methoxybenzoic acid (dicamba), as thin layers on submicron silica particles. The limits of detection of 4.8 µM and 0.6 µM were obtained for the sensing of glyphosate in chloroform and acetonitrile, respectively. The reported system shows promise for future application in the sensing of glyphosate through further optimization of the dye and the implementation of a biphasic assay with water/organic solvent mixtures for sensing in aqueous environmental samples.