@article{MuellerRueckJobstetal., author = {M{\"u}ller, Max and R{\"u}ck, Thomas and Jobst, Simon and Pangerl, Jonas and Weigl, Stefan and Bierl, Rudolf and Matysik, Frank-Michael}, title = {An Algorithmic Approach to Compute the Effect of Non-Radiative Relaxation Processes in Photoacoustic Spectroscopy}, series = {Photoacoustics}, volume = {26}, journal = {Photoacoustics}, publisher = {Elsevier}, doi = {10.1016/j.pacs.2022.100371}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:898-opus4-39935}, abstract = {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.}, language = {en} } @misc{vanderWeerdBierlMatysik, author = {van der Weerd, Bastiaan and Bierl, Rudolf and Matysik, Frank-Michael}, title = {A Conductivity Probe for Determination of the Carbon Dioxide Tension at the Oxygenator Exhaust Outlet during Extracorporeal Membrane Oxygenation (ECMO)}, series = {Proceedings of the 9th ISC Modern Analytical Chemistry 2013, Prag}, journal = {Proceedings of the 9th ISC Modern Analytical Chemistry 2013, Prag}, language = {en} } @misc{RueckMatysikBierl, author = {R{\"u}ck, Thomas and Matysik, Frank-Michael and Bierl, Rudolf}, title = {Development of a miniaturized photoacoustic multigas sensing system for trace gas measurement}, series = {analytica conference 2014, 1. bis 4. April, M{\"u}nchen}, journal = {analytica conference 2014, 1. bis 4. April, M{\"u}nchen}, language = {en} } @misc{RueckMatysikBierl, author = {R{\"u}ck, Thomas and Matysik, Frank-Michael and Bierl, Rudolf}, title = {Comparison of acoustic detectors for use in miniaturized photoacoustic devices designed for nitrogen dioxide trace gas measurement}, series = {ANAKON, 23.-26.3.2015, Graz}, journal = {ANAKON, 23.-26.3.2015, Graz}, language = {en} } @article{PangerlSukulRuecketal., author = {Pangerl, Jonas and Sukul, Pritam and R{\"u}ck, Thomas and Fuchs, Patricia and Weigl, Stefan and Miekisch, Wolfram and Bierl, Rudolf and Matysik, Frank-Michael}, title = {An inexpensive UV-LED photoacoustic based real-time sensor-system detecting exhaled trace-acetone}, series = {Photoacoustics}, volume = {38}, journal = {Photoacoustics}, publisher = {Elsevier}, issn = {2213-5979}, doi = {10.1016/j.pacs.2024.100604}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:898-opus4-71279}, pages = {12}, abstract = {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.}, language = {en} } @article{EscherRueckJobstetal., author = {Escher, Lukas and R{\"u}ck, Thomas and Jobst, Simon and Pangerl, Jonas and Bierl, Rudolf and Matysik, Frank-Michael}, title = {Photodissociation-Driven Photoacoustic Spectroscopy with UV-LEDs for Ozone Detection}, series = {Photoacoustics}, volume = {43}, journal = {Photoacoustics}, publisher = {Elsevier BV}, issn = {2213-5979}, doi = {10.1016/j.pacs.2025.100718}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:898-opus4-80076}, pages = {16}, abstract = {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.}, language = {en} } @article{WeiglFeldmeierBierletal., author = {Weigl, Stefan and Feldmeier, Florian and Bierl, Rudolf and Matysik, Frank-Michael}, title = {Photoacoustic detection of acetone in N2 and synthetic air using a high power UV LED}, series = {Sensors Actuators B Chemical}, volume = {316}, journal = {Sensors Actuators B Chemical}, number = {August}, publisher = {Elsevier}, doi = {10.1016/j.snb.2020.128109}, pages = {1 -- 11}, abstract = {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.}, language = {en} } @article{WeiglWittmannRuecketal., author = {Weigl, Stefan and Wittmann, Elisabeth and R{\"u}ck, Thomas and Bierl, Rudolf and Matysik, Frank-Michael}, title = {Effects of ambient parameters and cross-sensitivities from O2, CO2 and H2O on the photoacoustic detection of acetone in the UV region}, series = {Sensors Actuators B Chemical}, journal = {Sensors Actuators B Chemical}, number = {328}, publisher = {Elsevier}, issn = {0925-4005}, doi = {10.1016/j.snb.2020.129001}, abstract = {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.}, language = {en} } @unpublished{PangerlSukulRuecketal., author = {Pangerl, Jonas and Sukul, Pritam and R{\"u}ck, Thomas and Fuchs, Patricia and Weigl, Stefan and Miekisch, Wolfram and Bierl, Rudolf and Matysik, Frank-Michael}, title = {An Inexpensive Uv-Led Photoacoustic Based Real-Time Sensor-System Detecting Exhaled Trace-Acetone}, publisher = {Elsevier}, doi = {10.2139/ssrn.4724198}, abstract = {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.}, language = {en} } @article{RueckBierlMatysik, author = {R{\"u}ck, Thomas and Bierl, Rudolf and Matysik, Frank-Michael}, title = {NO2 trace gas monitoring in air using off-beam quartz enhanced photoacoustic spectroscopy (QEPAS) and interference studies towards CO2, H2O and acoustic noise}, series = {Sensors and Actuators B: Chemical}, volume = {255}, journal = {Sensors and Actuators B: Chemical}, number = {Part 3, February}, publisher = {Elsevier}, doi = {10.1016/j.snb.2017.09.039}, pages = {2462 -- 2471}, abstract = {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 per mille 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.}, language = {en} } @article{RueckBierlMatysik, author = {R{\"u}ck, Thomas and Bierl, Rudolf and Matysik, Frank-Michael}, title = {Development and characterization of a laboratory setup for photoacoustic NO2 determination based on the excitation of electronic 2B2 and 2B1 states using a low-cost semiconductor laser}, series = {Sensors and Actuators A: Physical}, volume = {258}, journal = {Sensors and Actuators A: Physical}, publisher = {Elsevier}, address = {Amsterdam, Niederlande}, doi = {10.1016/j.sna.2017.03.024}, pages = {193 -- 200}, abstract = {This work gives a detailed characterization of a laboratory setup for photoacoustic NO2 trace gas detection at the ppb level. The signal generation is based on the excitation of electronic 2B2 and 2B1 states using a low-cost semiconductor laser emitting at 450 nm. An acoustic resonator was used for signal amplification and the modulation frequency of the laser was determined to 3395 Hz in order to gain maximum signal amplification. The quality of resonant amplification was determined to 7.9. The gas samples were NO2 calibration gases diluted with pure nitrogen. The signal-to-noise ratio (SNR) dependency on the flow rate Q and the lock-in time constant τLIA was investigated, respectively, and the optimum values were specified to Q = 500 mL/min and τLIA = 2 s. In case of ambient noise, increasing τLIA to 10 s was evaluated as sufficient for SNR preservation. The noise level was measured in the absence of NO2 and it was determined to be composed of 51\% electronic noise and 49\% gas flow noise. With the analyte concentration ranging from 300 ppbV to 100 ppmV, the linear dependency of the photoacoustic amplitude on the NO2 concentration was specified, the sensitivity was determined to 110 μV/ppmV and the maximum measurement error was calculated to ±0.8\%. The detection limit was determined to 2.0 ppbV. Furthermore, the stability of the signal was investigated and a maximum drift of ±1\% was observed within a measuring period of 30 min. The response time τ90 was specified to 58 s. All results considered, this photoacoustic measuring system, which is based on low-cost signal generation and detection units, provides an excellent basis in view of developing a portable device for photoacoustic trace gas detection.}, language = {en} } @article{RueckBierlMatysik, author = {R{\"u}ck, Thomas and Bierl, Rudolf and Matysik, Frank-Michael}, title = {Low-cost photoacoustic NO2 trace gas monitoring at the pptV-level}, series = {Sensors and Actuators A: Physical}, volume = {263}, journal = {Sensors and Actuators A: Physical}, publisher = {Elsevier}, address = {Amsterdam, Niederlande}, doi = {10.1016/j.sna.2017.06.036}, pages = {501 -- 509}, abstract = {We present the development and the characterization of a photoacoustic NO2 trace gas detection system. The system is based on the implementation of low-cost components, i.e. a mass-produced blue diode laser and a standard MEMS microphone which is commonly built into smartphones, for example. An optimized cell design was realized by means of 3D printing. The linearity of the photoacoustic signal dependency on the analyte concentration was verified from 200 ppbV to 100 ppmV NO2. The detection limit (1σ) was determined to 33 pptV and the normalized noise equivalent absorption coefficient was calculated to 7.0 ∙ 10-10 W cm-1 Hz-1/2. The dynamic range of the system was verified to be linear over three magnitudes of order and the sensitivity was calculated to 814 μV/ppmV. The system was characterized in view of optimal operating parameters, i.e. lock-in time constant τLIA and total mass flow rate, optical performance and signal stability. The mass flow dependend response time of the system was specified to 19 s and an idealized step response to a quasi-Heaviside step function was quantified as a function of τLIA. The quality factor of acoustic resonance was determined to 21.9 and an empirical expression regarding acoustic node shifting is provided. The expression takes into account the radius of the resonator pipe and the radius of the hole, which was drilled into the pipe for microphone coupling. Furthermore, we studied the cross-sensitivity of the photoacoustic signal towards H2O and CO2, respectively.}, language = {en} } @misc{WeiglMatysikBierl, author = {Weigl, Stefan and Matysik, Frank-Michael and Bierl, Rudolf}, title = {Development of a sensor system for analysis of human breath exhale}, series = {BayWISS Herbstakademie 2018, Plankstetten}, journal = {BayWISS Herbstakademie 2018, Plankstetten}, abstract = {Atemgasanalyse ist ein junges und vielversprechendes Feld im Bereich der diagnostischen Medizin. Der Ansatz verspricht einfach zug{\"a}ngliche und leicht wiederholbare Probennahme die zum einen non-invasiv ist und zugleich R{\"u}ckschl{\"u}sse auf Vorg{\"a}nge im menschlichen K{\"o}rper und bspw. dessen Gesundheitszustand zul{\"a}sst. Seit Ende des 20. Jahrhunderts gibt es Massenspektrometer die es erm{\"o}glicht haben mehrere Tausend verschiedene Stoffe in der Ausatemluft nachzuweisen. Diese Technologien verbessern sich stetig und erm{\"o}glichen es die Vorg{\"a}nge und Zusammenh{\"a}nge zwischen Zusammensetzung der Ausatemluft und systemischen Prozessen besser zu verstehen. Die bei Studien mit Massenspektrometern ermittelten Biomarker, deren qualitative und quantitative Detektion Gesundheitsdiagnosen erm{\"o}glichen, haben aber noch nicht den Weg in den klinischen Alltag gefunden. Das Problem sind meistens die hohen Anschaffungskosten, komplizierte Datenauswertung und zumeist geringe Verf{\"u}gbarkeit und Immobilit{\"a}t dieser Messger{\"a}te. Die photoakustische Spektroskopie ist eine selektive und hochsensitive Messmethode, die es erm{\"o}glichen soll den Biomarker „Aceton", der grunds{\"a}tzlich die Metabolisierung von Fetten widerspiegelt, schnell und reproduzierbar quantitativ zu detektieren. Dabei m{\"u}ssen Hindernisse wie Querempfindlichkeiten, ausgel{\"o}st durch die komplexe Zusammensetzung der Messmatrix Atemgas, bei gleichzeitig kleine Aceton Konzentrationen (200-800 parts-per-billion) {\"u}berwunden werden. Verschiedene Wellenl{\"a}ngenbereiche mit unterschiedlichen Lichtquellen, akustisch resonante sowie innovative Messzellendesigns und anspruchsvolle Datenauswertung mittels komplexer Algorithmik sind n{\"o}tig um das Ziel, die Entwicklung eines kompakten, g{\"u}nstigen und zuverl{\"a}ssigen Acetonsensors, zu erreichen.}, language = {en} } @article{vanderWeerdBierlMatysik, author = {van der Weerd, Bastiaan and Bierl, Rudolf and Matysik, Frank-Michael}, title = {Trends in Electrochemical Sensing of Blood Gases}, series = {Bioanalytical Reviews}, volume = {6}, journal = {Bioanalytical Reviews}, publisher = {Springer}, address = {Berlin}, doi = {10.1007/11663_2016_1}, pages = {263 -- 280}, abstract = {The monitoring of partial pressures of the blood gases carbon dioxide (pCO2) and oxygen (pO2) is of great importance in clinical diagnostics. The measure of pCO2 and pO2 provides essential information about the patient's metabolism, gas exchange, ventilation, and acid-base homeostasis. The conventional electrochemical methods for clinical blood gas analysis are based on the potentiometric Severinghaus sensor for carbon dioxide and the amperometric Clark sensor for oxygen. These techniques are well established and are only shortly discussed in this overview. However, in recent years a variety of modifications of these classical sensor concepts and new approaches of electrochemical sensing of pCO2 and pO2 have been introduced. This review summarizes recent developments in this field and discusses the potential for future applications in clinical blood gas analysis.}, language = {en} } @inproceedings{RueckLandgrafLaeppleetal., author = {R{\"u}ck, Thomas and Landgraf, Ferdinand and L{\"a}pple, I. and Unger, J. and Matysik, Frank-Michael and Bierl, Rudolf}, title = {Specification of an improved photoacoustic setup for high-sensitive, low-cost NO2 trace gas detection}, series = {18th International Conference on Photoacoustic and Photothermal Phenomena (ICPPP18), 2015, September 6-10, Novi Sad, Serbia}, booktitle = {18th International Conference on Photoacoustic and Photothermal Phenomena (ICPPP18), 2015, September 6-10, Novi Sad, Serbia}, language = {en} } @inproceedings{vanderWeerdBierlMatysik, author = {van der Weerd, Bastiaan and Bierl, Rudolf and Matysik, Frank-Michael}, title = {A Conductivity Probe for the Determination of Carbon Dioxide Tension at the Oxygenator Exhaust Outlet during Extracorporeal Membrane Oxygenation (ECMO)}, series = {analytica Conference 2014, 1. bis 4. April, M{\"u}nchen}, booktitle = {analytica Conference 2014, 1. bis 4. April, M{\"u}nchen}, language = {en} } @inproceedings{vanderWeerdBierlMatysik, author = {van der Weerd, Bastiaan and Bierl, Rudolf and Matysik, Frank-Michael}, title = {A Conductivity Probe for the Determination of Carbon Dioxide Tension at the Oxygenator Exhaust Outlet during Extracorporeal Membrane Oxygenation (ECMO)}, series = {Electrochemistry 2014, September 22 - 24, Mainz}, booktitle = {Electrochemistry 2014, September 22 - 24, Mainz}, language = {en} } @inproceedings{vanderWeerdBierlMatysik, author = {van der Weerd, Bastiaan and Bierl, Rudolf and Matysik, Frank-Michael}, title = {A Planar Conductivity Probe for CO2 Determination at the Oxygenator Outlet}, series = {Doktorandenseminar GDCh Prozessanalytik 2014, Berlin}, booktitle = {Doktorandenseminar GDCh Prozessanalytik 2014, Berlin}, language = {en} } @article{BraunDurnerRabletal., author = {Braun, Peter and Durner, Bernhard and Rabl, Hans-Peter and Matysik, Frank-Michael}, title = {Investigations on the decomposition of AdBlue urea in the liquid phase at low temperatures by an electrochemically induced pH shift}, series = {Monatshefte f{\"u}r Chemie}, volume = {150}, journal = {Monatshefte f{\"u}r Chemie}, number = {9}, publisher = {Springer}, doi = {10.1007/s00706-019-02406-6}, pages = {1633 -- 1641}, abstract = {Ammonia-based selective catalytic reduction (SCR) systems are the most widely used technology for reduction of nitrogen oxide emissions from lean-burn engines such as diesel engines. However, at low exhaust temperatures, the SCR process is limited by difficulties in the decomposition of the ammonia precursor urea, which is carried on-board using an aqueous solution "AdBlue". In this study, the decomposition of AdBlue urea induced by electrical current and the resulting associated pH shifts were investigated in a divided cell configuration in the liquid phase. The decomposition was found to be favored in both electrochemical compartments, anodic and cathodic, at temperatures of 60-80 degrees C compared to a reference without electrochemical treatment. In addition to the determination of ammonia contents using an ammonia sensor, IC/HPLC analyses were carried out for each sample. Different side products such as biuret, nitrate, cyanuric acid, ammelide, and others were formed. In the anodic compartment, nitrate formation could be observed due to oxidation of ammonia at the electrode surface. [GRAPHICS] .}, language = {en} } @article{BraunRablMatysik, author = {Braun, Peter and Rabl, Hans-Peter and Matysik, Frank-Michael}, title = {Investigations on the Liquid-Phase Decomposition of AdBlue Urea for the Selective Catalytic Reduction Process}, series = {Chemie Ingenieur Technik}, volume = {91}, journal = {Chemie Ingenieur Technik}, number = {7}, publisher = {Wiley}, doi = {10.1002/cite.201800055}, pages = {961 -- 968}, abstract = {Difficulties in decomposing AdBlue to ammonia limit the applicability of selective catalytic reduction systems at low exhaust temperatures. Investigations on the decomposition of AdBlue in the liquid phase under elevated pressure at temperatures up to 165 degrees C were carried out. Besides effects of inorganic catalysts, the impact of pH on urea decomposition was examined. After dissolution in aqueous phase, the compounds ZnO, WO3, and MoO3 were found to be effective in liquid-phase AdBlue decomposition. However, the efficiency was dropping significantly over few hours. Decomposition of AdBlue urea was also found to be favored for alkaline and acidic conditions.}, language = {en} }