Refine
Year
Publication Type
- Article (331) (remove)
Language
- English (300)
- Multiple languages (16)
- German (15)
Keywords
- eu3+ (4)
- ce3+ (2)
- energy transfer (2)
- led (2)
- tb3+ (2)
- uranyl (2)
- Hydraulic Fracturing, Fracing (1)
- Lead · Pb · Hunting · Gunshot · Fertilizer · Soil contamination · Food contamination · Consumer risk (1)
- MMCT (1)
- Nitrogen generation Pressure swing adsorption Performance indicators Carbon molecular sieve Process intensification (1)
Faculty
- Chemieingenieurwesen (CIW) (331) (remove)
This study investigated the ability of electrically conductive carbon rovings to detect cracks in textile-reinforced concrete (TRC) structures. The key innovation lies in the integration of carbon rovings into the reinforcing textile, which not only contributes to the mechanical properties of the concrete structure but also eliminates the need for an additional sensory system, such as strain gauges, to monitor the structural health. Carbon rovings are integrated into a grid-like textile reinforcement that differs in binding type and dispersion concentration of the styrene butadiene rubber (SBR) coating. Ninety final samples were subjected to a four-point bending test in which the electrical changes of the carbon rovings were measured simultaneously to capture the strain. The mechanical results show that the SBR50-coated TRC samples with circular and elliptical cross-sectional shape achieved, with 1.55 kN, the highest bending tensile strength, which is also captured with a value of 0.65 Ω by the electrical impedance monitoring. The elongation and fracture of the rovings have a significant effect on the impedance mainly due to electrical resistance change. A correlation was found between the impedance change, binding type and coating. This suggests that the elongation and fracture mechanisms are affected by the number of outer and inner filaments, as well as the coating.
A new approach to determine the elements carbon, hydrogen, nitrogen and oxygen (CHNO) in polymers by wavelength-dispersive X-ray fluorescence analysis (WDXRF) in combination with partial least squares (PLS) regression was explored. The quantification of CHNO was achieved by using the Rayleigh and Compton scattering spectra of an Rh X-ray tube from 84 different polymers. Concealed differences of the corresponding scattering spectra could be utilized to quantify CHNO in a multivariate manner. It was shown that the developed model was capable of determining these commonly non-measurable matrix elements in polymers using WDXRF. Furthermore, the influence of spectral resolution, which is given by the collimator and the crystal, on the prediction of CHNO was explored in this study. It was found that minimal spectral resolution led to the most accurate CHNO predictions. Information about matrix composition could be used to improve so-called semi-quantitative XRF methods based on fundamental parameters (FP) for the analysis of plastics, soil or other samples with high organic content.
UV emitting nanoparticles enhance the effect of ionizing radiation in 3D lung cancer spheroids
(2022)
Crystallographic and Photoluminescence Studies on the Solid Solution Li3Ba2La3–xPrx(WO4)8 (x = 0-3
(2022)
Spectroscopic Studies on Pr3+ Doped LuPO4 and YPO4 upon VUV and Synchrotron Radiation Excitation
(2022)
This work deals with the spectroscopic properties of praseodymium doped single crystalline lutetium aluminum garnet (LuAG:Pr3+). A special focus was set on temperature- and time-dependent spectroscopy. Beyond the well-known down-conversion luminescence of LuAG:Pr3+, also UV-A/B up-conversion luminescence under excitation with a 488 nm laser was thoroughly investigated. Furthermore, the results of the spectroscopic investigations on the single crystalline material were supplemented and compared with measurements on a microscale powder sample.
In addition, to the spectroscopic investigations, mechanistic considerations are presented to obtain a closer look at the up-conversion process in LuAG:Pr3+. We promote the thesis of a temperature-dependent energy transfer up-conversion mechanism.
Different from negatively charged CuInS2 (CIS) based quantum dots (QDs), positively charged QDs are difficult to obtain in good optical quality, but are desirable for certain applications. We herein present a general synthesis strategy that allows for a universal surface modification of ternary CIS based QDs with thiol containing ligands.
The idea behind the synthesis design is, to apply a ZnS shell first for passivating and protecting the core QDs, and then add a second ZnS shell for the functionalization via ligand exchange. Whereby easy ligand exchange with thiolated molecules is systematically set up, by using a weak bonding amine ligand for the second shell. Molecules with various terminal groups were used to functionalize the nanoparticles and stabilize them in different media making any surface charge and polarity accessible. Surface defect chemistry seemed to play an important role in our synthesis strategy, therefore to gain a deeper understanding how these defect sites can alter the electronic structure of core/shell nanoparticles theoretical calculations based on density functional theory were performed, whilst structural, colloidal and optical properties were characterized experimentally (by dynamic light scattering, x-ray diffraction, infrared spectroscopy, zeta potential, absorption- and (time resolved) photoluminescence
measurements).
We report on a watt-level highly efficient europium laser operating at the 5D0→7F4 transition. It is based on the stoichiometric KEu(WO4)2 crystal. Under pumping by a green laser at 532.1 nm, the KEu(WO4)2 laser generated a maximum peak output power of 1.11 W at ∼703nm with a slope efficiency of 43.2% and a linear polarization (????‖????????). A laser threshold as low as 64 mW was achieved. True continuous-wave operation was demonstrated. The polarized emission properties of monoclinic KEu(WO4)2 were determined.
The quaternary tungstates Li3Ba2RE3(WO4)8 (RE = La-Nd, Sm-Ho) were obtained by a ceramic synthesis route and were characterized by powder and single crystal X-ray diffraction. The structures of Li3Ba2Pr3(WO4)8 and Li3Ba2Tb3(WO4)8 were refined from single crystal diffractometer data: RbLiBi2(MoO4)4 type, space group C2/c, a = 528.57(2), b = 1292.39(6), c = 1934.80(10) pm, b = 91.522(4)°, 2151 F2 values, 108 parameters for Li3Ba2Pr3(WO4)8 and a = 520.54(2), b = 1272.03(6), c = 1918.85(10) pm, b = 91.948(4)°, 2020 F2 values, 108 variables for Li3Ba2Tb3(WO4)8. Striking polyhedral building units in these tungstates are WO4 tetrahedra and LiO6 octahedra, while the mixed occupied site and the barium atoms have higher coordination numbers, i.e. RE/Li@O8 and Ba@O10. In addition to the powder quality assessment by means of reflection spectroscopy, the synthesized samples were studied for their suitability as a scintillator material. Therefore, X-ray excited luminescence measurements where performed. Apart from Li3Ba2Ce3(WO4)8 and Li3Ba2Nd3(WO4)8, all compounds show strong emission under X-ray irradiation. Li3Ba2La3(WO4)8 and Li3Ba2Gd3(WO4)8 show blue CT luminescence caused by tungstate units, while the other samples show typical and multiple lines due to well known [Xe]4fn → [Xe]4fn transitions.