TY - JOUR A1 - Tahri, K. A1 - Tiebe, Carlo A1 - El Bari, N. A1 - Hübert, Thomas A1 - Bouchikhi, B. T1 - Geographical provenience differentiation and adulteration detection of cumin by means of electronic sensing Systems and SPME-GC-MS in combination with different chemometric approaches JF - Analytical Methods N2 - The detection of the aroma and flavour volatile compounds of spices is key in product quality control. Accordingly, it is necessary to develop new electronic sensing systems for food adulteration control and authenticity assessment for protecting customer's health. In this work, the capability of the E-nose and VE-tongue in combination with SPME-GC-MS to correctly discriminate between several cumin samples of different geographical origins and to detect their adulteration, by using unsupervised and supervised chemometric tools, was evaluated. Regarding the aroma profile, eleven volatile compounds were characterized by SPME-GC-MS; all of them were found in cumin powder while only eight are found in cumin seeds. The main volatile compounds detected were b-pinene, m-cymene, g-terpinene, cuminaldehyde and cuminic alcohol, in different proportions depending on the cumin sample form (seed or powder). In summary, the results obtained are sufficiently encouraging as a starting point for the development of new electronic sensing systems with more improvement in the reliability of the sensor's performance as well as chemometric tools in order to deal with a complex dataset. KW - Voltammetric electronic tongue KW - Electronic nose KW - SPME-GC-MS KW - Chemometric tool KW - Cumin discrimination KW - Geographical origins KW - Adulteration detection PY - 2016 DO - https://doi.org/10.1039/c6ay01906d SN - 1759-9660 VL - 8 IS - 42 SP - 7638 EP - 7649 PB - RCS AN - OPUS4-38558 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hübert, Thomas A1 - Tiebe, Carlo A1 - Detjens, Marc A1 - Majewski, J. T1 - On-site calibration system for trace humidity sensors JF - Measurement N2 - A portable device for calibration of trace humidity sensors and an adopted calibration procedure have been developed. The calibration device is based on humidity generation by permeating water through polymeric membrane tubes. Water vapour transmission rates for various polymers were experimentally determined in order to select the most suitable polymeric material. The developed trace humidity generator consists of a gas-flow polymeric hose immersed in a water reservoir thermostated by a sensorcontrolled heater. Mole fractions of water vapour between 1 µmol/ molˉ¹ and 350 µmol/molˉ¹ (equivalent to frost-point temperatures from -76 °C to -31 °C) were generated by varying either the operating temperature or gas flow. The operating temperature can be varied from 20 °C to 60 °C and kept stable within 0.1 K. Uncertainty analysis indicated that the trace humidity generator produces gas flows of constant humidity amounts with a relative expanded uncertainty less than 3.4% (k = 2) of the generated value. KW - Polymeric tubes KW - Measurements KW - Trace Humidity KW - Sensor calibration KW - Water vapour permeation PY - 2016 DO - https://doi.org/10.1016/j.measurement.2016.05.013 SN - 0263-2241 VL - 91 IS - 9 SP - 251 EP - 257 PB - Elsevier Ltd. AN - OPUS4-36762 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Erwamati, F. U. A1 - Pratapa, S. A1 - Suasmoro, S. A1 - Hübert, Thomas A1 - Banach, Ulrich T1 - Preparation and structural study of Mg1−xZnxTiO3 ceramics and their dielectric properties from 1 Hz to 7.7 GHz JF - Journal of Materials Science: Materials in Electronics N2 - A series of Mg₁₋ₓZnₓTiO₃, x = 0–0.5 (MZT0–MZT0.5) ceramics was synthesised and characterised. The dielectric properties of the samples in the frequency range of 1 Hz – 7.7 GHz were explored using three different methods: a contacting electrode method, a parallel-plate method and a perturbed resonator method. The electrical properties in the space charge and dipolar polarisation frequency ranges are discussed in relation to the phase composition and microstructure data. Differences in the zinc Substitution divided the dielectrics into two groups, namely MZT0-MZT0.2 and MZT0.3–MZT0.5, each with different amount of a main Mg₁₋ₓZnₓTiO₃ solid solution phase and a secondary solid solution phase. Zinc substitution promoted the density of the ceramics, improved the purity of the main phase and increased the permittivity for frequencies up to 10⁸ Hz, but reduced the permittivity in the microwave range. In the MZT0.3–MZT0.5 samples, for frequencies less than 1 MHz the quality (Q x ƒ) factors were lower and log σ ₐ.c, the AC conductivity, was higher than for the MZT0–MZT0.2 samples. Above 10 MHz, the (Q x ƒ) factors and log σ ₐ.c of the two groups were similar. KW - Mg1-xZnxTiO3 KW - Space charge polarisation KW - Dipole polarisation KW - Microwave frequency KW - Dielectric properties PY - 2016 DO - https://doi.org/10.1007/s10854-016-4610-6 SN - 0957-4522 VL - 27 IS - 7 SP - 6637 EP - 6645 PB - Springer CY - Dordrecht, Netherlands AN - OPUS4-36466 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -