کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1162666 1490895 2016 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Active wavelength selection for mixture identification with tunable mid-infrared detectors
ترجمه فارسی عنوان
انتخاب طول موج فعال برای شناسایی مخلوط با آشکارسازهای نیمه مادون قرمز قابل تنظیم
کلمات کلیدی
انتخاب طول فعال شناسایی مخلوط، فابری پرت تداخل سنجی، رگرسیون فرآیند گاوسی، کوچکترین مربعات غیر منفی کوچک، تجزیه و تحلیل خطی خطی
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• An active wavelength-selection algorithm is proposed for mixture identification.
• The algorithm runs in real-time, interleaving wavelength selection with sensing.
• Wavelength selection is analyte-specific and based on previous measurements.
• Active wavelength selection operates in two stages: exploration and exploitation.
• The approach is compared against a passive strategy based on successive projection.

This article presents a wavelength selection framework for mixture identification problems. In contrast with multivariate calibration, where the mixture constituents are known and the goal is to estimate their concentration, in mixture identification the goal is to determine which of a large number of chemicals is present. Due to the combinatorial nature of this problem, traditional wavelength selection algorithms are unsuitable because the optimal set of wavelengths is mixture dependent. To address this issue, our framework interleaves wavelength selection with the sensing process, such that each subsequent wavelength is determined on-the-fly based on previous measurements. To avoid early convergence, our approach starts with an exploratory criterion that samples the spectrum broadly, then switches to an exploitative criterion that selects increasingly more relevant wavelengths as the solution approaches the true constituents of the mixture. We compare this “active” wavelength selection algorithm against a state-of-the-art passive algorithm (successive projection algorithm), both experimentally using a tunable spectrometer and in simulation using a large spectral library of chemicals. Our results show that our active method can converge to the true solution more frequently and with fewer measurements than the passive algorithm. The active method also leads to more compact solutions with fewer false positives.

Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Analytica Chimica Acta - Volume 937, 21 September 2016, Pages 11–20
نویسندگان
, ,