TY - JOUR A1 - Müller, Max A1 - Rück, Thomas A1 - Jobst, Simon A1 - Pangerl, Jonas A1 - Weigl, Stefan A1 - Bierl, Rudolf A1 - Matysik, Frank-Michael T1 - An Algorithmic Approach to Compute the Effect of Non-Radiative Relaxation Processes in Photoacoustic Spectroscopy JF - Photoacoustics N2 - Successful transfer of photoacoustic gas sensors from laboratory to real-life applications requires knowledge about potential cross-sensitivities towards environmental and gas matrix changes. Multi-dimensional calibration in case of cross-sensitivities can become very complex or even unfeasible. To address this challenge, we present a novel algorithm to compute the collision based non-radiative efficiency and phase lag of energy relaxation on a molecular level (CoNRad) for photoacoustic signal calculation. This algorithmic approach allows to calculate the entire elaxation cascade of arbitrarily complex systems, yielding a theoretical photoacoustic signal. In this work the influence of varying bulk compositions, i.e. nitrogen (N2), oxygen (O2) and water (H2O) on the photoacoustic signal during methane (CH4) detection is demonstrated. The applicability of the algorithm to other photoacoustic setups is shown exemplary by applying it to the relaxational system investigated in [1]. Hayden et al. examined the effect of water on photoacoustic carbon monoxide (CO) detection. Y1 - 2022 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:898-opus4-39935 N1 - Corresponding author: Max Müller VL - 26 PB - Elsevier ER - TY - GEN A1 - van der Weerd, Bastiaan A1 - Bierl, Rudolf A1 - Matysik, Frank-Michael T1 - A Conductivity Probe for Determination of the Carbon Dioxide Tension at the Oxygenator Exhaust Outlet during Extracorporeal Membrane Oxygenation (ECMO) T2 - Proceedings of the 9th ISC Modern Analytical Chemistry 2013, Prag Y1 - 2013 UR - https://www.gdch.de/fileadmin/downloads/Veranstaltungen/Tagungen/2014_Tagungen/analytica/poster_abstracts/sens03_vanderweerd_5860.pdf ER - TY - GEN A1 - Rück, Thomas A1 - Matysik, Frank-Michael A1 - Bierl, Rudolf T1 - Development of a miniaturized photoacoustic multigas sensing system for trace gas measurement T2 - analytica conference 2014, 1. bis 4. April, München Y1 - 2014 UR - https://www.gdch.de/fileadmin/downloads/Veranstaltungen/Tagungen/2014_Tagungen/analytica/poster_abstracts/sens05_rueck_5925.pdf ER - TY - GEN A1 - Rück, Thomas A1 - Matysik, Frank-Michael A1 - Bierl, Rudolf T1 - Comparison of acoustic detectors for use in miniaturized photoacoustic devices designed for nitrogen dioxide trace gas measurement T2 - ANAKON, 23.-26.3.2015, Graz Y1 - 2015 ER - TY - JOUR A1 - Pangerl, Jonas A1 - Sukul, Pritam A1 - Rück, Thomas A1 - Fuchs, Patricia A1 - Weigl, Stefan A1 - Miekisch, Wolfram A1 - Bierl, Rudolf A1 - Matysik, Frank-Michael T1 - An inexpensive UV-LED photoacoustic based real-time sensor-system detecting exhaled trace-acetone JF - Photoacoustics N2 - n this research we present a low-cost system for breath acetone analysis based on UV-LED photoacoustic spectroscopy. We considered the end-tidal phase of exhalation, which represents the systemic concentrations of volatile organic compounds (VOCs) – providing clinically relevant information about the human health. This is achieved via the development of a CO2-triggered breath sampling system, which collected alveolar breath over several minutes in sterile and inert containers. A real-time mass spectrometer is coupled to serve as a reference device for calibration measurements and subsequent breath analysis. The new sensor system provided a 3σ detection limit of 8.3 ppbV and an NNEA of 1.4E-9 Wcm 1Hz 0.5. In terms of the performed breath analysis measurements, 12 out of 13 fell within the error margin of the photoacoustic measurement system, demonstrating the reliability of the measurements in the field. KW - Photoacoustic spectroscopy KW - Real-time mass-spectrometry KW - Breath analysis KW - Acetone KW - UV-LED Y1 - 2024 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:898-opus4-71279 SN - 2213-5979 N1 - Corresponding author der OTH Regensburg: Jonas Pangerl VL - 38 PB - Elsevier ER - TY - JOUR A1 - Escher, Lukas A1 - Rück, Thomas A1 - Jobst, Simon A1 - Pangerl, Jonas A1 - Bierl, Rudolf A1 - Matysik, Frank-Michael T1 - Photodissociation-Driven Photoacoustic Spectroscopy with UV-LEDs for Ozone Detection JF - Photoacoustics N2 - This study presents the development and evaluation of a UV-LED based photoacoustic (PA) measurement system for ozone (O3) detection to demonstrate its potential for low-cost and accurate sensing while for the first time addressing the importance of photodissociation for PA signal generation for O3 in the UV range. With a detection limit of 7.9 ppbV, the system exhibits a significant advancement over state-of-the-art UV-PA O3 detection and is on par with laser-based setups. Following a novel discussion of the PA signal arising from photodissociation and its products, cross-sensitivity effects due to environmental factors such as temperature and gas composition were systematically analyzed. A digital twin driven compensation for these influences was implemented and evaluated. Despite the challenges associated with modeling the effects of H2O and CO2, the PA system shows considerable potential, though further studies in real world applications must be conducted. KW - Photoacoustic spectroscopy KW - UV-LED KW - Ozone KW - Photodissociation KW - Cross-sensitivity Y1 - 2025 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:898-opus4-80076 SN - 2213-5979 N1 - Corresponding author der OTH Regensburg: Lukas Escher VL - 43 PB - Elsevier BV ER - TY - JOUR A1 - Weigl, Stefan A1 - Feldmeier, Florian A1 - Bierl, Rudolf A1 - Matysik, Frank-Michael T1 - Photoacoustic detection of acetone in N2 and synthetic air using a high power UV LED JF - Sensors Actuators B Chemical N2 - The performance of a photoacoustic trace gas sensor for the detection of acetone in N2 and synthetic air is reported. The sensor system utilises an amplitude modulated UV LED. The light source has an emission maximum at 278 nm and a maximum CW output power of 300 mW according to the datasheet. Three different collimating and focusing approaches have been investigated to guide the highly divergent LED light into the acoustic resonator of the photoacoustic measurement cell. A 3D printed aluminium cell was designed to optimize light coupling by simultaneously minimizing the photoacoustic background signal generation. Hence, the diameter of the resonator was set to a comparable large diameter of 10 mm and the inner walls of the resonator were mirror polished. The additive manufacturing procedure allowed for integration of a spirally formed gas channel, enabling gas heating prior to detection. The sensor performance was investigated by measuring acetone in N2 and synthetic air at different concentrations. The UV LED current was set to 86 % of the maximum value according to the datasheet of the light source in order to increase the lifetime and thermal stability. An Allan-Werle deviation analysis validates a stable sensor performance. The limit of detection (LoD) was determined at a 3σ noise level with a 10 s lock-in amplifier time constant by sampling data points over 20 s with a data acquisition rate of 5 Hz. LoDs of 80.8 ppbV and 19.6 ppbV were obtained for acetone in N2 and synthetic air, respectively. KW - Acetone detection KW - Photoacoustic spectroscopy KW - High power UV LED KW - UV LED collimation system KW - Acetone breath analysis Y1 - 2020 U6 - https://doi.org/10.1016/j.snb.2020.128109 N1 - Corresponding author at: Sensorik-Applikationszentrum (SappZ) der Ostbayerischen Technischen Hochschule Regensburg VL - 316 IS - August SP - 1 EP - 11 PB - Elsevier ER - TY - JOUR A1 - Weigl, Stefan A1 - Wittmann, Elisabeth A1 - Rück, Thomas A1 - Bierl, Rudolf A1 - Matysik, Frank-Michael T1 - Effects of ambient parameters and cross-sensitivities from O2, CO2 and H2O on the photoacoustic detection of acetone in the UV region JF - Sensors Actuators B Chemical N2 - We present a sensitive UV LED photoacoustic setup for the detection of gaseous acetone and discuss its applicability towards breath analysis. We investigated the performance of the sensor for low acetone concentrations down to 0.1 parts per million (ppmV). The influences of temperature, flow, pressure, optical power and LED duty cycle on the measured signal have been examined. To gain a better understanding of the different effects on the photoacoustic signal, correlation analysis was applied and feature importance was determined using a large measured dataset. Furthermore, the cross-sensitivities towards O2, CO2 and H2O have been studied extensively. Finally, the sensor’s performance to detect acetone between 0.1–1 ppmV within gas mixtures simulating breath exhale conditions has been investigated, too. With a limit of detection (LoD) of 12.5 parts per billion (ppbV) (3σ) measured under typical breath exhale gas mixture conditions, the sensor demonstrated a high potential for the application of acetone detection in human breath analysis. KW - Acetone detection KW - Photoacoustic spectroscopy KW - High power UV LED KW - Cross-sensitivities KW - Acetone breath analysis Y1 - 2021 U6 - https://doi.org/10.1016/j.snb.2020.129001 SN - 0925-4005 N1 - Corresponding authors: Stefan Weigl, Elisabeth Wittmann, Thomas Rück, Rudolf Bierl, Frank-Michael Matysik N1 - Corrigendum to “Effects of ambient parameters and cross-sensitivities from O2, CO2 and H2O on the photoacoustic detection of acetone in the UV region” [Sens. Actuators B: Chem. 328 (February 2021) (2020) 129001]; https://doi.org/10.1016/j.snb.2020.129392 IS - 328 PB - Elsevier ER - TY - INPR A1 - Pangerl, Jonas A1 - Sukul, Pritam A1 - Rück, Thomas A1 - Fuchs, Patricia A1 - Weigl, Stefan A1 - Miekisch, Wolfram A1 - Bierl, Rudolf A1 - Matysik, Frank-Michael T1 - An Inexpensive Uv-Led Photoacoustic Based Real-Time Sensor-System Detecting Exhaled Trace-Acetone N2 - In this research we present a low-cost system for breath acetone analysis based on UV-LED photoacoustic spectroscopy. We considered the end-tidal phase of exhalation, which represents the systemic concentrations of volatile organic compounds (VOCs) – providing clinically relevant information about the human health. This is achieved via the development of a CO2-triggered breath sampling system, which collected alveolar breath over several minutes in sterile and inert containers. A real-time mass spectrometer is coupled to serve as a reference device for calibration measurements and subsequent breath analysis. The new sensor system provided a 3σ detection limit of 6.4 ppbV and an NNEA of 1.1E-9 Wcm-1Hz-0.5. In terms of the performed breath analysis measurements, 12 out of 13 fell within the error margin of the photoacoustic measurement system, demonstrating the reliability of the measurements in the field. KW - photoacoustic spectroscopy KW - real-time mass-spectrometry KW - breath analysis KW - acetone KW - UV-LED Y1 - 2024 U6 - https://doi.org/10.2139/ssrn.4724198 N1 - Der Aufsatz wurde peer-reviewed unter folgender DOI veröffentlicht: https://doi.org/10.1016/j.pacs.2024.100604 PB - Elsevier ER - TY - JOUR A1 - Rück, Thomas A1 - Bierl, Rudolf A1 - Matysik, Frank-Michael T1 - NO2 trace gas monitoring in air using off-beam quartz enhanced photoacoustic spectroscopy (QEPAS) and interference studies towards CO2, H2O and acoustic noise JF - Sensors and Actuators B: Chemical N2 - We present the development and characterization as well as comprehensive interference studies of a photoacoustic NO2 trace gas detection system. The system is based on an off-beam quartz enhanced photoacoustic scheme (off-beam QEPAS) and signal generation was initiated by amplitude modulating a low-cost diode laser emitting at 450 nm. The QEPAS sensor element features double-resonant amplification, still it is only ∼ 5 × 5 × 2.5 mm in size. The individual and combined resonance characteristics were investigated and specified to 52 dB amplification, adding up 15 dB acoustic- and 37 dB mechanical-resonance amplification. The linearity of the photoacoustic signal dependency on the analyte concentration was verified from 200 ppbV to 100 ppmV NO2 in synthetic air. The detection limit (3σ) was determined to 1.8 ppbV using a lock-in time constant of 10 s and an averaging time of 20 s. The normalized noise equivalent absorption coefficient was specified to 2.5·10−8 W cm−1 Hz−0.5. The stability of the signal was investigated over time and a slight drift by 1‰ was observed after 30 min without temperature stabilizing the photoacoustic cell (PAC). Noise analysis was performed by means of Allan deviation and the inverse dependency of response time and precision of the system on the lock-in time constant was outlined. We performed interference analyses towards N2, O2, CO2, H2O and acoustic noise, respectively. Although neither spectral interferences nor losses due to slow NO2 VT-relaxation were observed, O2 was identified to cause a 15% signal drop due to VVNO2-O2-relaxation. Changing H2O concentrations were found to cause acoustic detuning, which cannot be compensated by adjusting the frequency of modulation, because of the double-resonant feature of the PAC. However, alternative approaches of compensation were discussed. Finally, we carried out heavy traffic noise simulations and determined the QEPAS setup to be 46 times less susceptible towards ambient noise compared to standard microphone-based photoacoustic setups. Y1 - 2018 U6 - https://doi.org/10.1016/j.snb.2017.09.039 VL - 255 IS - Part 3, February SP - 2462 EP - 2471 PB - Elsevier ER -