ACTIVE ANALYSIS OF CHEMICAL MIXTURES WITH MULTI-MODAL SPARSE NON-NEGATIVE LEAST SQUARES

New sensor technologies such as Fabry-Pérot interferometers (FPI) offer low-cost and portable alternatives to traditional infrared absorption spectroscopy for chemical analysis. However, with FPIs the absorption spectrum has to be measured one wavelength at a time. In this work, we propose an active-sensing framework to select a subset of wavelengths that best separates the specific components of a chemical mixture. Compared to passive featureselection approaches, in which the subset is selected offline, active sensing selects the next feature on-the-fly based on previous measurements so as to reduce uncertainty. We propose a novel multi-modal non-negative least squares method (MM-NNLS) to solve the underlying linear system, which has multiple nearoptimal solutions. We tested the framework on mixture problems of up to 10 components from a library of 100 chemicals. MM-NNLS can solve complex mixtures using only a small number of measurements, and outperforms passive approaches in terms of sensing efficiency and stability. Index Terms—Active sensing, tunable sensors, multi-modal optimization, chemical mixture analysis.

Active Wavelength Selection for Chemical Identification Using Tunable Spectroscopy

Spectrometers are the cornerstone of analytical chemistry. Recent advances in microoptics manufacturing provide lightweight and portable alternatives to traditional spectrometers. In this dissertation, we developed a spectrometer based on Fabry-Perot interferometers (FPIs). A FPI is a tunable (it can only scan one wavelength at a time) optical filter. However, compared to its traditional counterparts such as FTIR (Fourier transform infrared spectroscopy), FPIs provide lower resolution and lower signal-noiseratio (SNR). Wavelength selection can help alleviate these drawbacks. Eliminating uninformative wavelengths not only speeds up the sensing process but also helps improve accuracy by avoiding nonlinearity and noise. Traditional wavelength selection algorithms follow a training-validation process, and thus they are only optimal for the target analyte. However, for chemical identification, the identities are unknown. To address the above issue, this dissertation proposes active sensing algorithms that select wavelengths online while sensing. These algorithms are able to generate analytedependent wavelengths. We envision this algorithm deployed on a portable chemical gas platform that has low-cost sensors and limited computation resources. We develop three algorithms focusing on three different aspects of the chemical identification problems. First, we consider the problem of single chemical identification. We formulate the problem as a typical classification problem where each chemical is considered as a distinct class. We use Bayesian risk as the utility function for wavelength selection, which calculates the misclassification cost between classes (chemicals), and we select the wavelength with the maximum reduction in the risk. We evaluate this approach on both synthesized and experimental data. The results suggest that active sensing outperforms the passive method, especially in a noisy environment. Second, we consider the problem of chemical mixture identification. Since the number of potential chemical mixtures grows exponentially as the number of components increases, it is intractable to formulate all potential mixtures as classes. To circumvent combinatorial explosion, we developed a multi-modal non-negative least squares (MMNNLS) method that searches multiple near-optimal solutions as an approximation of all the solutions. We project the solutions onto spectral space, calculate the variance of the projected spectra at each wavelength, and select the next wavelength using the variance as the guidance. We validate this approach on synthesized and experimental data. The results suggest that active approaches are superior to their passive counterparts especially when the condition number of the mixture grows larger (the analytes consist of more components, or the constituent spectra are very similar to each other). Third, we consider improving the computational speed for chemical mixture identification. MM-NNLS scales poorly as the chemical mixture becomes more complex. Therefore, we develop a wavelength selection method based on Gaussian process regression (GPR). GPR aims to reconstruct the spectrum rather than solving the mixture problem, thus, its computational cost is a function of the number of wavelengths. We evaluate the approach on both synthesized and experimental data. The results again demonstrate more accurate and robust performance in contrast to passive algorithms

Active Wavelength Selection for Chemical Identification Using Tunable Spectroscopy

Spectrometers are the cornerstone of analytical chemistry. Recent advances in microoptics manufacturing provide lightweight and portable alternatives to traditional spectrometers. In this dissertation, we developed a spectrometer based on Fabry-Perot interferometers (FPIs). A FPI is a tunable (it can only scan one wavelength at a time) optical filter. However, compared to its traditional counterparts such as FTIR (Fourier transform infrared spectroscopy), FPIs provide lower resolution and lower signal-noiseratio (SNR). Wavelength selection can help alleviate these drawbacks. Eliminating uninformative wavelengths not only speeds up the sensing process but also helps improve accuracy by avoiding nonlinearity and noise. Traditional wavelength selection algorithms follow a training-validation process, and thus they are only optimal for the target analyte. However, for chemical identification, the identities are unknown. To address the above issue, this dissertation proposes active sensing algorithms that select wavelengths online while sensing. These algorithms are able to generate analytedependent wavelengths. We envision this algorithm deployed on a portable chemical gas platform that has low-cost sensors and limited computation resources. We develop three algorithms focusing on three different aspects of the chemical identification problems. First, we consider the problem of single chemical identification. We formulate the problem as a typical classification problem where each chemical is considered as a distinct class. We use Bayesian risk as the utility function for wavelength selection, which calculates the misclassification cost between classes (chemicals), and we select the wavelength with the maximum reduction in the risk. We evaluate this approach on both synthesized and experimental data. The results suggest that active sensing outperforms the passive method, especially in a noisy environment. Second, we consider the problem of chemical mixture identification. Since the number of potential chemical mixtures grows exponentially as the number of components increases, it is intractable to formulate all potential mixtures as classes. To circumvent combinatorial explosion, we developed a multi-modal non-negative least squares (MMNNLS) method that searches multiple near-optimal solutions as an approximation of all the solutions. We project the solutions onto spectral space, calculate the variance of the projected spectra at each wavelength, and select the next wavelength using the variance as the guidance. We validate this approach on synthesized and experimental data. The results suggest that active approaches are superior to their passive counterparts especially when the condition number of the mixture grows larger (the analytes consist of more components, or the constituent spectra are very similar to each other). Third, we consider improving the computational speed for chemical mixture identification. MM-NNLS scales poorly as the chemical mixture becomes more complex. Therefore, we develop a wavelength selection method based on Gaussian process regression (GPR). GPR aims to reconstruct the spectrum rather than solving the mixture problem, thus, its computational cost is a function of the number of wavelengths. We evaluate the approach on both synthesized and experimental data. The results again demonstrate more accurate and robust performance in contrast to passive algorithms

Détection, localisation et quantification de déplacements par capteurs à fibre optique

For structural health monitoring, optical fiber sensors are mostly used thanks their capacity to provide distributed measurements. Based on the principle of Brillouin scattering, optical fiber sensors measure Brillouin frequency profile, sensitive to strain and temperature into the optical fiber, with a meter spatial resolution over several kilometers. The first problem is to obtain a centimeter spatial resolution with the same sensing length. To solve it, source separation, deconvolution and resolution of inverse problem methodologies are used. Then, the athermal strain into the structure is searched. Several algorithms based on adaptative filter are tested to correct the thermal effect on strain measurements. Finally, several methods are developed to quantify structure displacements from the athermal strain measurements. They have been tested on simulated and controlled-conditions dataPour l’auscultation d’ouvrages, les capteurs à fibre optique sont généralement utilisés puisqu’ils présentent l’avantage de fournir des mesures réparties. Plus particulièrement, le capteur basé sur la technologie Brillouin permet d’acquérir un profil de fréquence Brillouin, sensible à la température et la déformation dans une fibre optique sur une dizaine de kilomètres avec un pas de l’ordre de la dizaine de centimètres. La première problématique est d’obtenir un profil centimétrique sur la même longueur d’auscultation. Nous y répondons en s’appuyant sur des méthodes de séparation de sources, de déconvolution et de résolution de problèmes inverses. Ensuite, nous souhaitons estimer la déformation athermique dans l’ouvrage. Pour cela, plusieurs algorithmes de filtrage adaptatif sont comparés. Finalement, un procédé pour quantifier le déplacement de l’ouvrage à partir des mesures de déformation est proposé. Toutes ces méthodes sont testés sur des données simulées et réelles acquises dans des conditions contrôlées