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Search Results (332)

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14 pages, 3701 KiB  
Article
Smart E-Tongue Based on Polypyrrole Sensor Array as Tool for Rapid Analysis of Coffees from Different Varieties
by Alvaro Arrieta Almario, Oriana Palma Calabokis and Eisa Arrieta Barrera
Foods 2024, 13(22), 3586; https://doi.org/10.3390/foods13223586 - 10 Nov 2024
Viewed by 493
Abstract
Due to the lucrative coffee market, this product is often subject to adulteration, as inferior or non-coffee materials or varieties are mixed in, negatively affecting its quality. Traditional sensory evaluations by expert tasters and chemical analysis methods, although effective, are time-consuming, costly, and [...] Read more.
Due to the lucrative coffee market, this product is often subject to adulteration, as inferior or non-coffee materials or varieties are mixed in, negatively affecting its quality. Traditional sensory evaluations by expert tasters and chemical analysis methods, although effective, are time-consuming, costly, and require skilled personnel. The aim of this work was to evaluate the capacity of a smart electronic tongue (e-tongue) based on a polypyrrole sensor array as a tool for the rapid analysis of coffees elaborated from beans of different varieties. The smart e-tongue device was developed with a polypyrrole-based voltammetric sensor array and portable multi-potentiostat operated via smartphone. The sensor array comprised seven electrodes, each doped with distinct counterions to enhance cross-selectivity. The smart e-tongue was tested on five Arabica coffee varieties (Typica, Bourbon, Maragogype, Tabi, and Caturra). The resulting voltammetric signals were analyzed using principal component analysis assisted by neural networks (PCNN) and cluster analysis (CA), enabling clear discrimination among the coffee samples. The results demonstrate that the polypyrrole sensors can generate distinct electrochemical patterns, serving as “fingerprints” for each coffee variety. This study highlights the potential of polypyrrole-based smart e-tongues as a rapid, cost-effective, and portable alternative for coffee quality assessment and adulteration detection, with broader applications in the food and beverage industry. Full article
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<p>Scheme of functional analogy between the human taste system and an e-tongue and its parts (sample; sensory array; multi-channel system; and pattern recognition system).</p>
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<p>Chemical structure of doping ions used in the preparation of the PPy sensor array.</p>
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<p>Image of the smart e-tongue device and its parts (sensor array, multi-potentiostat, and data recording and processing system).</p>
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<p>Schematic of oxidation/reduction processes in PPy sensors where cation exchange (process I) and anion exchange (process II) are presented.</p>
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<p>Reproducibility of (<b>a</b>) the voltammetric signals of 50 cycles of the S7 sensor (PPy/TSA) against a coffee sample from Maragogype variety beans and (<b>b</b>) Voltammetric signals recorded by different S5 sensors (PPy/DBS) in replicates of Typica variety bean coffee prepared in different batches. The lines represent all the replicates of the voltammetric signals of each sensor.</p>
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<p>Voltammetric signals recorded by the sensor array against a coffee sample prepared with Caturra variety beans as instance of sensor redox response variability that contributes to cross-selectivity.</p>
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<p>Voltammetric signals of the lithium perchlorate/S1 doped sensor (PPy/PC) versus coffee samples prepared with beans of different varieties as instance of response variability and cross-selectivity.</p>
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<p>Loading graph resulting from PCNN analysis on the data matrix recorded with the smart e-tongue on the analyzed coffee samples: red-S1 (PPyPC); purple-S2 (PPyFCN); green-S3 (PPy/SF); fuchsia-S4 (PPy/SO4); yellow-S5 (PPy/DBS); grey-S6 (PPy/AQDS); and blue-S7 (PPy/TSA).</p>
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<p>Score graph resulting from the PCNN analysis on the data matrix recorded with the smart e-tongue on the analyzed coffee samples.</p>
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<p>Dendrogram of cluster analysis for coffee samples elaborated with beans of different varieties.</p>
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12 pages, 1914 KiB  
Article
Computational Design of the Electronic Response for Volatile Organic Compounds Interacting with Doped Graphene Substrates
by Li Chen, David Bodesheim, Ahmad Ranjbar, Arezoo Dianat, Robert Biele, Rafael Gutierrez, Mohammad Khazaei and Gianaurelio Cuniberti
Nanomaterials 2024, 14(22), 1778; https://doi.org/10.3390/nano14221778 - 5 Nov 2024
Viewed by 619
Abstract
Changes in the work function provide a fingerprint to characterize analyte binding in charge transfer-based sensor devices. Hence, a rational sensor design requires a fundamental understanding of the microscopic factors controlling the modification of the work function. In the current investigation, we address [...] Read more.
Changes in the work function provide a fingerprint to characterize analyte binding in charge transfer-based sensor devices. Hence, a rational sensor design requires a fundamental understanding of the microscopic factors controlling the modification of the work function. In the current investigation, we address the mechanisms behind the work function change (WFC) for the adsorption of four common volatile organic compounds (toluene, ethanol, 2-Furfurylthiol, and guaiacol) on different nitrogen-doped graphene-based 2D materials using density functional theory. We show that competition between the surface dipole moment change induced by spatial charge redistribution, the one induced by the pure adsorbate, and the one caused by the surface deformation can quantitatively predict the work function change. Furthermore, we also show this competition can explain the non-growing work function change behavior in the increasing concentrations of nitrogen-doped graphenes. Finally, we propose possible design principles for WFC of VOCs interacting with N-doped graphene materials. Full article
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<p>Ball-and-stick representation of VOC molecules and graphene-based substrates.</p>
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<p>Heatmap of work function change <math display="inline"><semantics> <mrow> <mo>Δ</mo> <mi>ϕ</mi> </mrow> </semantics></math> comparisons among different odorant–substrate combinations. The labeled number indicates the corresponding work function change value.</p>
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<p>Comparison of trends in the absolute value of work function change <math display="inline"><semantics> <mrow> <mo>Δ</mo> <mi>ϕ</mi> </mrow> </semantics></math> and charge transfer <span class="html-italic">Q</span> of the substrates towards the adsorption of (<b>a</b>) toluene, (<b>b</b>) ethanol, (<b>c</b>) 2-Furfurylthiol, and (<b>d</b>) guaiacol.</p>
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<p>Linear correlation between work function change <math display="inline"><semantics> <mrow> <mo>Δ</mo> <mi>ϕ</mi> </mrow> </semantics></math> (<span class="html-italic">y</span>-axis) and surface dipole moment change <math display="inline"><semantics> <mrow> <mo>Δ</mo> <msub> <mi>P</mi> <mi>tot</mi> </msub> </mrow> </semantics></math> (<span class="html-italic">x</span>-axis). The straight solid and dashed lines present the fitted and referred linear correlation, respectively.</p>
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<p>Total surface dipole moment change decomposition for 2-Furfurylthiol adsorbed on 4pd-N substrate. (<b>a</b>) Components of surface deformation <math display="inline"><semantics> <msub> <mi>p</mi> <mi mathvariant="normal">s</mi> </msub> </semantics></math> − <math display="inline"><semantics> <msub> <mi>p</mi> <mn>0</mn> </msub> </semantics></math>. (<b>b</b>) Surface dipole moment resulting from the deformation of the VOC molecule upon adsorption <math display="inline"><semantics> <msub> <mi>p</mi> <mi mathvariant="normal">a</mi> </msub> </semantics></math>. (<b>c</b>) <math display="inline"><semantics> <mrow> <mo>Δ</mo> <msub> <mi>p</mi> <mi>cplx</mi> </msub> </mrow> </semantics></math> owing to the spatial charge redistribution in the complex adsorbate–adsorbent system. (<b>d</b>) Charge density difference distribution <math display="inline"><semantics> <mrow> <mo>Δ</mo> <mi>n</mi> </mrow> </semantics></math> of the <span class="html-italic">x</span>–<span class="html-italic">y</span> planar average along the <span class="html-italic">z</span> direction. The grey circle is the location of the substrate, and the area between the two orange circles is the adsorbate location, where the lowest and highest atoms of the VOC molecule are denoted by the two atoms. In (<b>c</b>,<b>d</b>), the curve is divided into several regions: (1), (3) blue areas indicating electron depletion and (2) red area indicating electron accumulation. The dense dashed line denotes the highest position for <math display="inline"><semantics> <mrow> <mo>Δ</mo> <msub> <mi>p</mi> <mi>cplx</mi> </msub> <mo>=</mo> <mn>0</mn> </mrow> </semantics></math>, and the sign of <math display="inline"><semantics> <mrow> <mo>Δ</mo> <mi>n</mi> </mrow> </semantics></math> is labeled in (<b>d</b>).</p>
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<p>The same as <a href="#nanomaterials-14-01778-f005" class="html-fig">Figure 5</a>, but for GR-N.</p>
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<p>Histograms of total surface dipole moment change decomposition for (<b>a</b>) toluene, (<b>b</b>) ethanol, (<b>c</b>) 2-Furfurylthiol, and (<b>d</b>) guaiacol. The variation in the negative total surface dipole moment change <math display="inline"><semantics> <mrow> <mo>Δ</mo> <msub> <mi>P</mi> <mi>tot</mi> </msub> </mrow> </semantics></math> and the distribution of the components <math display="inline"><semantics> <mrow> <mo>Δ</mo> <msub> <mi>p</mi> <mi>cplx</mi> </msub> </mrow> </semantics></math>, <math display="inline"><semantics> <msub> <mi>p</mi> <mi mathvariant="normal">a</mi> </msub> </semantics></math>, and <math display="inline"><semantics> <mrow> <msub> <mi>p</mi> <mi mathvariant="normal">s</mi> </msub> <mo>−</mo> <msub> <mi>p</mi> <mn>0</mn> </msub> </mrow> </semantics></math> are presented.</p>
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16 pages, 3872 KiB  
Article
Classification of Sesame Oil Based on Processing-Originated Differences in the Volatile Organic Compound Profile by a Colorimetric Sensor
by Tianyi Liu, Hai-Ming Shi, Untzizu Elejalde and Xiaodong Chen
Foods 2024, 13(20), 3230; https://doi.org/10.3390/foods13203230 - 11 Oct 2024
Viewed by 820
Abstract
Fragrant edible sesame oil is popular for its unique aroma. The aroma of sesame oil is determined by its volatile organic compound (VOC) profile. Sesame oils produced by different techniques could have different VOC profiles. In addition, blending fragrant sesame oil with refined [...] Read more.
Fragrant edible sesame oil is popular for its unique aroma. The aroma of sesame oil is determined by its volatile organic compound (VOC) profile. Sesame oils produced by different techniques could have different VOC profiles. In addition, blending fragrant sesame oil with refined oil could also alter the VOC profile of the final product. Current practices in aroma analysis, such as sensory evaluation and gas chromatography (GC), still face many restraints. Hence, there is a need for alternatives. We present a novel 14-unit multiplexed paper-based colorimetric sensor for fragrant sesame oil VOC analysis. The sensor was designed to visualize the VOC profile as a color “fingerprint”. The sensor was validated with 55 branded sesame oil samples produced by two different techniques, i.e., hot pressing and small milling; the experimental results suggested a processing dependency in color VOC fingerprints. The sensor also demonstrated the potential to detect the change in sesame oil VOC profile due to blending with refined oil, with an estimated limit of detection down to 20% v/v of the refined oil. The colorimetric sensor might be used as a simple, rapid, and cost-effective analytical tool in the production and quality control of fragrant sesame oil. Full article
(This article belongs to the Section Food Engineering and Technology)
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<p>(<b>a</b>) A colorimetric sensor array was proposed as a rapid, simple, and low-cost alternative to the current practice for fragrant sesame oil VOC analysis; information on sesame oil properties can be easily derived from the colorimetric VOC “fingerprint” generated by the sensor. (<b>b</b>) The sensor comprised 14 paper-based sensing units, each acting as a colorimetric receptor. The sensor demonstrated the potential to classify fragrant sesame oil samples produced by hot pressing and small milling based on their VOCs and to detect refined oil in fragrant sesame oil. On the principal component analysis (PCA) plot: red dots—small-milled sesame oil samples; blue-dots—hot-pressed sesame oil samples; grayscale symbols—suspected adulterated hot-pressed sesame oil samples.</p>
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<p>(<b>a</b>) The architecture and dimensions of the 14-unit colorimetric sensor. The chemical compositions of the receptors can be found in <a href="#app1-foods-13-03230" class="html-app">Supplementary Information S1</a>. (<b>b</b>) A schematic illustration of the sensing device. The sensing device consisted of a sample chamber, a sensor chamber, and a micro vacuum pump powered by a portable power source. (<b>c</b>) A flowchart of the sensing procedures. The images of the sensor were acquired with a desktop scanner; digital color information was extracted using ImageJ 1.53a (Wayne Rasband, National Institutes of Health, Bethesda, MD, USA) and subjected to further analysis.</p>
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<p>The scanned images and corresponding color difference maps generated by the sensor after exposure to common VOCs in food (for visualization, the color range of 0–167 was expanded to the 8-bit color range). The sensory attributes of the VOCs are included. The 14 receptors demonstrated different affinity to various VOCs, indicating the cross-reactive nature of the sensor.</p>
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<p>(<b>a</b>) Concentrations of major VOCs in the two authentic sesame oil samples measured using HS-SPME-GC analysis. The same groups of VOCs were detected in both HP-S and XM-S, yet the exact composition showed slight variation. (<b>b</b>) The PCA result based on the Euclidean distance values obtained by the colorimetric sensor array in response to the VOCs of HP-S and XM-S. HP-S and XM-S were clearly separated by PC1. Insets: average color difference maps of the two standards; HP-S produced stronger signals than XM-S, especially in receptor Nos. 5, 7, 8, and 11.</p>
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<p>The VOC profiles of the hot-pressed and small-milled samples from (<b>a</b>) Brand A, (<b>b</b>) Brand C, and (<b>c</b>) Brand O. For products from the same brand, the hot-pressed sample always contained more volatile acids and aldehydes (indicated by the arrows).</p>
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<p>(<b>a</b>) Typical scanned images of the colorimetric sensor array after exposure to hot-pressed (HP) and small-milled (XM) samples. Differences in the color fingerprints could be easily observed the naked eye. (<b>b</b>) The average color difference maps of commercial hot-pressed and small-milled samples. Compared with small-milled samples, hot-pressed samples generally produced more significant color changes, especially in sensing unit Nos. 5, 7, 8, and 11. (<b>c</b>) The color difference maps of hot-pressed and small-milled samples from Brands A, C, and O. For products from the same brand, the hot-pressed sample always produced stronger signals. (<b>d</b>) PCA results of 53 commercial samples; hot-pressed samples with normal color difference maps, hot-pressed samples with abnormal color difference maps, and small-milled samples are marked by blue, grayscale, and red symbols, respectively. Most hot-pressed samples clustered in the region of positive PC1 values, while most small-milled samples were found in the region of negative PC1 values. Among hot-pressed samples, some were found to produce less significant color changes; these samples were separated from the other hot-pressed samples by PC2 values.</p>
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<p>(<b>a</b>) The color difference maps of selected normal hot-pressed samples (from Brands A, C, E, and F) and abnormal hot-pressed samples (from Brands B, D, G, H, and J). Stronger signals were detected from normal hot-pressed samples, especially by receptor Nos. 7, 8, and 11. (<b>b</b>) Total lignan contents of the selected commercial hot-pressed samples. Samples with abnormal color difference maps generally had lower lignan contents, except Brand B. A low lignan content suggested that refined oil might be present.</p>
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<p>(<b>a</b>) The average color difference maps of samples containing various volume percentages of fragrant sesame oil. As the volume percentage of fragrant sesame oil increased, the signals detected by the sensor became stronger; the color difference map of blended sesame oil containing more than 80% <span class="html-italic">v</span>/<span class="html-italic">v</span> of fragrant sesame oil closely resembled that of the pure sesame oil. (<b>b</b>) PCA result. Refined oil samples formed a cluster that was clearly separated from that of pure sesame oil; as the volume percentage of refined oil decreased, the PC1 value became more positive; when the percentage decreased to 20% <span class="html-italic">v</span>/<span class="html-italic">v</span>, the clusters started to overlap. (<b>c</b>) PLS regression analysis result. With 9 PLS components selected, an r<sup>2</sup> value of 0.9423 could be obtained, suggesting a reasonably strong correlation.</p>
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23 pages, 10692 KiB  
Article
Intelligent Fault Diagnosis Method for Constant Pressure Variable Pump Based on Mel-MobileViT Lightweight Network
by Yonghui Zhao, Anqi Jiang, Wanlu Jiang, Xukang Yang, Xudong Xia and Xiaoyang Gu
J. Mar. Sci. Eng. 2024, 12(9), 1677; https://doi.org/10.3390/jmse12091677 - 19 Sep 2024
Viewed by 706
Abstract
The sound signals of hydraulic pumps contain abundant key information reflecting their internal mechanical states. In environments characterized by high temperatures or high-speed rotation, or where sensor deployment is challenging, acoustic sensors offer non-contact and flexible arrangement features. Therefore, this study aims to [...] Read more.
The sound signals of hydraulic pumps contain abundant key information reflecting their internal mechanical states. In environments characterized by high temperatures or high-speed rotation, or where sensor deployment is challenging, acoustic sensors offer non-contact and flexible arrangement features. Therefore, this study aims to develop an intelligent fault diagnosis method for hydraulic pumps based on acoustic signals. Initially, the Adaptive Chirp Mode Decomposition (ACMD) method is employed to remove environmental noise from the acoustic signals, enhancing the feature signals. Subsequently, the Mel spectrum is extracted as the acoustic fingerprint features of various fault states of the hydraulic pump, and these features are used to train the MobileViT network, achieving accurate identification of the different fault modes. The results indicate that the proposed Mel-MobileViT model effectively identifies and classifies various faults in constant pressure variable pumps, outperforming other models. This study not only provides an efficient and reliable intelligent method for the fault diagnosis of critical industrial equipment such as hydraulic pumps, but also offers new perspectives on the application of deep learning in acoustic pattern analysis. Full article
(This article belongs to the Section Ocean Engineering)
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<p>Convolutional neural network structure.</p>
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<p>MobileViT network architecture.</p>
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<p>The simulated signal includes complex time-varying signals and noise. <math display="inline"><semantics> <mrow> <mi>s</mi> <mo>(</mo> <mi>t</mi> <mo>)</mo> </mrow> </semantics></math>: (<b>a</b>) time-domain waveform; (<b>b</b>) spectrum.</p>
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<p>ACMD algorithm results (blue: true; red: ACMD): (<b>a</b>) time-domain waveform comparison; (<b>b</b>) frequency comparison.</p>
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<p>The time-frequency distribution of the simulated signal: (<b>a</b>) CWT; (<b>b</b>) STFT; (<b>c</b>) ACMD.</p>
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<p>The processing results of the proposed simulation signal by the EMD, VMD, and ACMD algorithms: (<b>a</b>) the spectrum of the original signal; (<b>b</b>) the spectrum of the ACMD modal components; (<b>c</b>) the spectrum of the reconstructed signal from EMD; (<b>d</b>) the spectrum of the reconstructed signal from VMD (K = 8); (<b>e</b>) the EMD component spectrum; and (<b>f</b>) the VMD component spectrum.</p>
Full article ">Figure 6 Cont.
<p>The processing results of the proposed simulation signal by the EMD, VMD, and ACMD algorithms: (<b>a</b>) the spectrum of the original signal; (<b>b</b>) the spectrum of the ACMD modal components; (<b>c</b>) the spectrum of the reconstructed signal from EMD; (<b>d</b>) the spectrum of the reconstructed signal from VMD (K = 8); (<b>e</b>) the EMD component spectrum; and (<b>f</b>) the VMD component spectrum.</p>
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<p>Fault diagnosis process.</p>
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<p>The schematic diagram of the hydraulic system of the constant pressure variable pump fault simulation test bench.</p>
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<p>Sensor installation position of constant pressure variable pump fault simulation test system.</p>
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<p>Physical images of constant pressure variable pump components with faults: (<b>a</b>) slipper pad wear (normal, light, severe); (<b>b</b>) loose slipper (normal, light, severe); (<b>c</b>) plunger wear (normal, light, severe); (<b>d</b>) inner race bearing fault; (<b>e</b>) outer race bearing fault; (<b>f</b>) rolling element bearing fault.</p>
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<p>Mel spectrogram sample construction process.</p>
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<p>Acoustic signal of plunger failure: (<b>a</b>) fault signal time domain; (<b>b</b>) spectrogram.</p>
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<p>Sound signals of plunger fault after ACMD processing: (<b>a</b>) reconstructed signal time domain; (<b>b</b>) spectrum of the reconstructed signal.</p>
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<p>Mel spectrograms of hydraulic pump under various fault conditions: (<b>a</b>) normal; (<b>b</b>) slipper boots (light); (<b>c</b>) slipper boots (heavy); (<b>d</b>) loose boots (light); (<b>e</b>) loose boots (heavy); (<b>f</b>) plunger (light); (<b>g</b>) plunger (heavy); (<b>h</b>) bearing inner ring; (<b>i</b>) bearing outer ring; (<b>j</b>) rolling element.</p>
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<p>Training loss and accuracy curves for Mel-MobileViT: (<b>a</b>) training loss; (<b>b</b>) training accuracy.</p>
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<p>Confusion matrices for different configurations of MobileViT: (<b>a</b>) S; (<b>b</b>) XS; (<b>c</b>) XXS.</p>
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<p>Confusion matrices for different configurations of MobileViT: (<b>a</b>) S; (<b>b</b>) XS; (<b>c</b>) XXS.</p>
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<p>Clustering effect of each layer of network: (<b>a</b>) Input data; (<b>b</b>) Layer 1; (<b>c</b>) Layer 5; (<b>d</b>) Layer 6.</p>
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<p>Clustering effect of each layer of network: (<b>a</b>) Input data; (<b>b</b>) Layer 1; (<b>c</b>) Layer 5; (<b>d</b>) Layer 6.</p>
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<p>Confusion matrices: (<b>a</b>) MobileViT-XXS; (<b>b</b>) MobileNetV1; (<b>c</b>) MobileNetV2.</p>
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10 pages, 3134 KiB  
Communication
All-Dielectric Metasurface-Based Terahertz Molecular Fingerprint Sensor for Trace Cinnamoylglycine Detection
by Qiyuan Xu, Mingjun Sun, Weijin Wang and Yanpeng Shi
Biosensors 2024, 14(9), 440; https://doi.org/10.3390/bios14090440 - 13 Sep 2024
Viewed by 929
Abstract
Terahertz (THZ) spectroscopy has emerged as a superior label-free sensing technology in the detection, identification, and quantification of biomolecules in various biological samples. However, the limitations in identification and discrimination sensitivity of current methods impede the wider adoption of this technology. In this [...] Read more.
Terahertz (THZ) spectroscopy has emerged as a superior label-free sensing technology in the detection, identification, and quantification of biomolecules in various biological samples. However, the limitations in identification and discrimination sensitivity of current methods impede the wider adoption of this technology. In this article, a meticulously designed metasurface is proposed for molecular fingerprint enhancement, consisting of a periodic array of lithium tantalate triangular prism tetramers arranged in a square quartz lattice. The physical mechanism is explained by the finite-difference time-domain (FDTD) method. The metasurface achieves a high quality factor (Q-factor) of 231 and demonstrates excellent THz sensing capabilities with a figure of merit (FoM) of 609. By varying the incident angle of the THz wave, the molecular fingerprint signal is strengthened, enabling the highly sensitive detection of trace amounts of analyte. Consequently, cinnamoylglycine can be detected with a sensitivity limit as low as 1.23 μg·cm2. This study offers critical insights into the advanced application of THz waves in biomedicine, particularly for the detection of urinary biomarkers in various diseases, including gestational diabetes mellitus (GDM). Full article
(This article belongs to the Special Issue Photonics for Bioapplications: Sensors and Technology)
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<p>(<b>a</b>) The structural diagram of the all-dielectric metasurface, illustrating the periodic arrangement of the high-index triangular prism tetramer based on the quartz substrate; (<b>b</b>) a unit cell of the periodic structure with a y-polarized source incident downwards in the z direction; (<b>c</b>) the main view of the unit cell (y–z plane) and corresponding parameters.</p>
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<p>(<b>a</b>) Transmission spectra for x-polarized and y-polarized incident waves at 0°; (<b>b</b>) transmission spectra for x-polarized and y-polarized incident waves at 37°; (<b>c</b>) the electric and magnetic field distribution measured at the surface of the quartz substrate at vertical incidence. The left and right figures correspond to the x-polarized and y-polarized incident wave, respectively.</p>
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<p>(<b>a</b>) Transmission spectra at different incident angles without any analyte; (<b>b</b>) the experimentally measured refractive index (n) and extinction coefficient (k) of cinnamoylglycine across the relevant frequency range; (<b>c</b>) transmission spectra at different incident angles with a <math display="inline"><semantics> <mrow> <mn>1</mn> <mo> </mo> <mi mathvariant="sans-serif">μ</mi> <mi mathvariant="normal">m</mi> </mrow> </semantics></math> thick layer of analyte; (<b>d</b>) the electric field distribution measured at the substrate surface in the x–y plane at 0.487 THz for specific incident angles, corresponding to the transmission spectra shown in (<b>c</b>), respectively.</p>
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<p>(<b>a</b>) Comprehensive transmission spectra without any analyte, with the incident angle ranging from 13° to 70°. Specifically, the rightmost line represents the transmission curve for an angle of 13°, while the leftmost line corresponds to 70°; (<b>b</b>) comprehensive transmission spectra with <math display="inline"><semantics> <mrow> <mn>1</mn> <mo> </mo> <mi mathvariant="sans-serif">μ</mi> <mi mathvariant="normal">m</mi> </mrow> </semantics></math> thick cinnamoylglycine, with the incident angle ranging from 13° to 62°. The corresponding envelope curve has been plotted by red line in the figure.</p>
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<p>(<b>a</b>) Transmission envelope curves for analytes of varying thicknesses; (<b>b</b>) the relationship between the thickness of the analyte and the transmission at <math display="inline"><semantics> <mrow> <mn>0.487</mn> <mo> </mo> <mi mathvariant="normal">T</mi> <mi mathvariant="normal">H</mi> <mi mathvariant="normal">z</mi> </mrow> </semantics></math>.</p>
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18 pages, 4659 KiB  
Article
Automated Room-Level Localisation Using Building Plan Information
by Mathias Thorsager, Sune Kroeyer, Adham Taha, Magnus Melgaard, Linette Anil, Jimmy Nielsen and Tatiana Madsen
Sensors 2024, 24(17), 5753; https://doi.org/10.3390/s24175753 - 4 Sep 2024
Viewed by 486
Abstract
Building Management Systems (BMSs) are transitioning from utilising wired installations to wireless Internet of Things (IoT) sensors and actuators. This shift introduces the requirement of robust localisation methods which can link the installed sensors to the correct Control Units (CTUs) which will facilitate [...] Read more.
Building Management Systems (BMSs) are transitioning from utilising wired installations to wireless Internet of Things (IoT) sensors and actuators. This shift introduces the requirement of robust localisation methods which can link the installed sensors to the correct Control Units (CTUs) which will facilitate continued communication. In order to lessen the installation burden on the technicians, the installation process should be made more complicated by the localisation method. We propose an automated version of the fingerprinting-based localisation method which estimates the location of sensors with room-level accuracy. This approach can be used for initialisation and maintenance of BMSs without introducing additional manual labour from the technician installing the sensors. The method is extended to two proposed localisation methods which take advantage of knowledge present in the building plan regarding the distribution of sensors in each room to estimate the location of groups of sensors at the same time. Through tests using a simulation environment based on a Bluetooth-based measurement campaign, the proposed methods showed an improved accuracy from the baseline automated fingerprinting method. The results showed an error rate of 1 in 20 sensors (if the number of sensors per room is known) or as few as 1 per 200 sensors (if a group of sensors are deployed and detected together for one room at a time). Full article
(This article belongs to the Special Issue Sensing Technologies and Wireless Communications for Industrial IoT)
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<p>General structure of the communication between the BMS hardware devices in a building plan consisting of six rooms. The red circles indicate IoT devices such as sensors, the blue boxes are control units which connect to the sensors and receive the sensing data, and the green boxes are access points which forward data from CTUs to the BMS.</p>
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<p>Experimental setup of RSSI measurements using two mobile phones. (<b>a</b>) Shows the equipment used for all measurements, and (<b>b</b>) shows the additional measurement locations for the transmitter to counteract the spatial fading.</p>
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<p>Building plan used for the measurement campaign as well as the tests. Tx<sub>1</sub> and Tx<sub>2</sub> depict the transmitter locations for the measurement campaign with the coloured letters depicting the receiver locations for the respective transmitter locations. The two Xs indicate the locations of the CTUs repeated in each room.</p>
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<p>Fitted RSSI model using parameters shown in <a href="#sensors-24-05753-t001" class="html-table">Table 1</a> plotted against the measured values shown in <a href="#sensors-24-05753-f003" class="html-fig">Figure 3</a> normalised for the wall attenuation. The point close to 0 m is an additional measurement point taken with both measurement devices placed in the same location.</p>
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<p>Heatmap showing the probability of correctly estimating a sensor using the single-sensor method for any location in the 8 rooms of the example building plan.</p>
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<p>Accuracy of the proposed methods as a function of the WAF <math display="inline"><semantics> <mi>β</mi> </semantics></math>.</p>
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<p>Accuracy of the proposed methods as a function of the std of the noise <math display="inline"><semantics> <msub> <mi>σ</mi> <mi>ξ</mi> </msub> </semantics></math>.</p>
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<p>Accuracy of the proposed methods as a function of the path loss exponent <math display="inline"><semantics> <mi>α</mi> </semantics></math>.</p>
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<p>Overview of sensor locations for the real-world validation test. The building plan follows the same layout as the one used in the RSSI model fitting measurement campaign. The circles indicate the locations of sensors, and the letters and numbers are used as identifiers for each sensor (the number identifies which room the sensor is in, and the letters distinguish the position of a sensor in a room). The Xs indicate the locations of the CTUs in each room.</p>
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12 pages, 14201 KiB  
Article
Development of Novel Surface-Enhanced Raman Spectroscopy-Based Biosensors by Controlling the Roughness of Gold/Alumina Platforms for Highly Sensitive Detection of Pyocyanin Secreted from Pseudomonas aeruginosa
by Waleed A. El-Said, Tamer S. Saleh, Abdullah Saad Al-Bogami, Mohmmad Younus Wani and Jeong-woo Choi
Biosensors 2024, 14(8), 399; https://doi.org/10.3390/bios14080399 - 19 Aug 2024
Viewed by 954
Abstract
Pyocyanin is considered a maker of Pseudomonas aeruginosa (P. aeruginosa) infection. Pyocyanin is among the toxins released by the P. aeruginosa bacteria. Therefore, the development of a direct detection of PYO is crucial due to its importance. Among the different optical [...] Read more.
Pyocyanin is considered a maker of Pseudomonas aeruginosa (P. aeruginosa) infection. Pyocyanin is among the toxins released by the P. aeruginosa bacteria. Therefore, the development of a direct detection of PYO is crucial due to its importance. Among the different optical techniques, the Raman technique showed unique advantages because of its fingerprint data, no sample preparation, and high sensitivity besides its ease of use. Noble metal nanostructures were used to improve the Raman response based on the surface-enhanced Raman scattering (SERS) technique. Anodic metal oxide attracts much interest due to its unique morphology and applications. The porous metal structure provides a large surface area that could be used as a hard template for periodic nanostructure array fabrication. Porous shapes and sizes could be controlled by controlling the anodization parameters, including the anodization voltage, current, temperature, and time, besides the metal purity and the electrolyte type/concentration. The anodization of aluminum foil results in anodic aluminum oxide (AAO) formation with different roughness. Here, we will use the roughness as hotspot centers to enhance the Raman signals. Firstly, a thin film of gold was deposited to develop gold/alumina (Au/AAO) platforms and then applied as SERS-active surfaces. The morphology and roughness of the developed substrates were investigated using scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques. The Au/AAO substrates were used for monitoring pyocyanin secreted from Pseudomonas aeruginosa microorganisms based on the SERS technique. The results showed that the roughness degree affects the enhancement efficiency of this sensor. The high enhancement was obtained in the case of depositing a 30 nm layer of gold onto the second anodized substrates. The developed sensor showed high sensitivity toward pyocyanin with a limit of detection of 96 nM with a linear response over a dynamic range from 1 µM to 9 µM. Full article
(This article belongs to the Special Issue The Emerging Techniques in Biosensors and Bioelectronics)
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<p>(<b>a</b>) SEM image of the electro-polished aluminum substrate, (<b>b</b>) SEM image of aluminum foil after first anodization, (<b>c</b>) SEM image of aluminum foil after second anodization, (<b>d</b>) SEM image of Au/electro-polished aluminum substrate, (<b>e</b>) SEM image of Au/first anodized aluminum foil, (<b>f</b>) SEM image of Au/second anodized aluminum foil, (<b>g</b>) AFM image of Au/electro-polished aluminum substrate, (<b>h</b>) AFM image of Au/first anodized aluminum foil, and (<b>i</b>) AFM image of Au/second anodized aluminum foil.</p>
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<p>SEM image with different magnifications of second anodized aluminum foil after depositing (<b>a</b>–<b>c</b>) 20 nm of Au, (<b>d</b>–<b>f</b>) 30 nm of Au, and (<b>g</b>–<b>i</b>) 50 nm of Au.</p>
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<p>(<b>a</b>) 3D AFM of electro-polished Al foil, (<b>b</b>) histogram of electro-polished Al foil, (<b>c</b>) 3D AFM of Au<sub>20nm</sub> modified electro-polished Al foil, (<b>d</b>) histogram of Au<sub>20nm</sub> modified electro-polished Al foil, (<b>e</b>) 3D AFM of first anodized Al foil, (<b>f</b>) histogram of first anodized Al foil, (<b>g</b>) 3D AFM of Au<sub>20nm</sub> modified first anodized Al foil, (<b>h</b>) histogram of Au<sub>20nm</sub> modified first anodized Al foil, (<b>i</b>) 3D AFM of second anodized Al foil, (<b>j</b>) histogram of second anodized Al foil, (<b>k</b>) 3D AFM of Au<sub>20nm</sub> modified second anodized Al foil, (<b>l</b>) histogram of Au<sub>20nm</sub> modified second anodized Al foil, (<b>m</b>) 3D AFM of Au<sub>30nm</sub> modified second anodized Al foil, (<b>n</b>) histogram of Au<sub>30nm</sub> modified second anodized Al foil, (<b>o</b>) 3D AFM of Au<sub>50nm</sub> modified second anodized Al foil, and (<b>p</b>) histogram of Au<sub>50nm</sub> modified second anodized Al foil.</p>
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<p>(<b>a</b>) SERS spectra of MBA immobilized on (green curve) Au<sub>20nm</sub> modified electro-polished Al substrate, (pink curve) Au<sub>20nm</sub> modified first anodized Al substrate, (blue curve) Au<sub>20nm</sub> modified second anodized Al substrate, (red curve) Au<sub>30nm</sub> modified second anodized Al substrate, and (black curve) Au<sub>50nm</sub> modified second anodized Al substrate, and (<b>b</b>) SERS spectra of MBA immobilized on three Al/Au<sub>30nm</sub> substrates.</p>
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<p>(<b>a</b>) SERS spectra of different concentrations of PYO using Au<sub>30nm</sub> modified second anodized Al substrate, (<b>b</b>) relationship between the intensity of Raman peak at 1398 cm<sup>−1</sup> and the PYO concentration using Au<sub>30nm</sub> modified second anodized Al substrate, and (<b>c</b>) SERS spectrum of PYO released from <span class="html-italic">P. aeruginosa</span> sample using Au<sub>30nm</sub> modified second anodized Al substrate.</p>
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<p>Design and fabrication of Au/AAO SERS-active surface for sensing PYO biomarker.</p>
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22 pages, 3397 KiB  
Article
Application of Spatial Offset Raman Spectroscopy (SORS) and Machine Learning for Sugar Syrup Adulteration Detection in UK Honey
by Mennatullah Shehata, Sophie Dodd, Sara Mosca, Pavel Matousek, Bhavna Parmar, Zoltan Kevei and Maria Anastasiadi
Foods 2024, 13(15), 2425; https://doi.org/10.3390/foods13152425 - 31 Jul 2024
Cited by 3 | Viewed by 6739
Abstract
Honey authentication is a complex process which traditionally requires costly and time-consuming analytical techniques not readily available to the producers. This study aimed to develop non-invasive sensor methods coupled with a multivariate data analysis to detect the type and percentage of exogenous sugar [...] Read more.
Honey authentication is a complex process which traditionally requires costly and time-consuming analytical techniques not readily available to the producers. This study aimed to develop non-invasive sensor methods coupled with a multivariate data analysis to detect the type and percentage of exogenous sugar adulteration in UK honeys. Through-container spatial offset Raman spectroscopy (SORS) was employed on 17 different types of natural honeys produced in the UK over a season. These samples were then spiked with rice and sugar beet syrups at the levels of 10%, 20%, 30%, and 50% w/w. The data acquired were used to construct prediction models for 14 types of honey with similar Raman fingerprints using different algorithms, namely PLS-DA, XGBoost, and Random Forest, with the aim to detect the level of adulteration per type of sugar syrup. The best-performing algorithm for classification was Random Forest, with only 1% of the pure honeys misclassified as adulterated and <3.5% of adulterated honey samples misclassified as pure. Random Forest was further employed to create a classification model which successfully classified samples according to the type of adulterant (rice or sugar beet) and the adulteration level. In addition, SORS spectra were collected from 27 samples of heather honey (24 Calluna vulgaris and 3 Erica cinerea) produced in the UK and corresponding subsamples spiked with high fructose sugar cane syrup, and an exploratory data analysis with PCA and a classification with Random Forest were performed, both showing clear separation between the pure and adulterated samples at medium (40%) and high (60%) adulteration levels and a 90% success at low adulteration levels (20%). The results of this study demonstrate the potential of SORS in combination with machine learning to be applied for the authentication of honey samples and the detection of exogenous sugars in the form of sugar syrups. A major advantage of the SORS technique is that it is a rapid, non-invasive method deployable in the field with potential application at all stages of the supply chain. Full article
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<p>SORS spectra corresponding to the 17 pure honeys collected in Year 2 before (<b>A</b>) and after (<b>B</b>) preprocessing.</p>
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<p>PCA plot of the SORS spectra acquired for honeys, sugar syrups, and sugar aqueous solutions. Pure honeys (H1–H17) are coloured in green, sugar beet syrups (b01 and b05–b07) in blue, and rice syrups (r01–r04 and r06–r08) in orange. The two blanks are water, while the individual sugars fructose (f), glucose (g), sucrose (s), and maltose (m) are 50, 25, and 12.5% <span class="html-italic">w</span>/<span class="html-italic">v</span> aqueous solutions.</p>
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<p>PCA plots showing the clustering of the 14 pure honeys and their corresponding rice syrup-spiked samples at different adulteration levels (<b>A</b>) and the clustering of the 14 pure honeys and their corresponding sugar beet syrup-spiked samples at different adulteration levels (<b>B</b>). Orange diamonds = pure honeys, red circles = 10% adulteration, blue triangles = 20% adulteration, green crosses = 30% adulteration, and purple exes = 50% adulteration. The ellipses represent 95% confidence ellipses for each group.</p>
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<p>PCA plot based on the SORS spectra of 27 pure heather honeys and 18 heather samples spiked with 20, 40, and 60% partially inverted sugar cane syrup. The number after the underscore represents the percentage of adulteration for each sample. SC = syrup sample.</p>
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<p>A scatter plot showing actual vs. predicted adulteration percentage for a random RF regression model for rice syrup adulteration (<b>A</b>) and sugar beet syrup adulteration (<b>B</b>). The solid line represents y = x (perfect agreement between predictions and ground truth), while the top and bottom dashed lines represent y = x + 3 and y = x – 3 respectively.</p>
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<p>Variable importance for rice and sugar beet classification models. Plot (<b>A</b>) shows the variable importance for one of the rice models, and (<b>B</b>) shows the SORS spectra for one of the pure honeys and its rice-spiked corresponding samples. Plot (<b>C</b>) shows the variable importance for one of the sugar beet models, while (<b>D</b>) shows the SORS spectra of one of the pure honeys with its sugar beet-adulterated samples. The arrows and boxes point to the Raman shift areas identified as significant for the model accuracy.</p>
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15 pages, 2200 KiB  
Article
Enhancing Indoor Positioning Accuracy with WLAN and WSN: A QPSO Hybrid Algorithm with Surface Tessellation
by Edgar Scavino, Mohd Amiruddin Abd Rahman, Zahid Farid, Sadique Ahmad and Muhammad Asim
Algorithms 2024, 17(8), 326; https://doi.org/10.3390/a17080326 - 25 Jul 2024
Viewed by 965
Abstract
In large indoor environments, accurate positioning and tracking of people and autonomous equipment have become essential requirements. The application of increasingly automated moving transportation units in large indoor spaces demands a precise knowledge of their positions, for both efficiency and safety reasons. Moreover, [...] Read more.
In large indoor environments, accurate positioning and tracking of people and autonomous equipment have become essential requirements. The application of increasingly automated moving transportation units in large indoor spaces demands a precise knowledge of their positions, for both efficiency and safety reasons. Moreover, satellite-based Global Positioning System (GPS) signals are likely to be unusable in deep indoor spaces, and technologies like WiFi and Bluetooth are susceptible to signal noise and fading effects. For these reasons, a hybrid approach that employs at least two different signal typologies proved to be more effective, resilient, robust, and accurate in determining localization in indoor environments. This paper proposes an improved hybrid technique that implements fingerprinting-based indoor positioning using Received Signal Strength (RSS) information from available Wireless Local Area Network (WLAN) access points and Wireless Sensor Network (WSN) technology. Six signals were recorded on a regular grid of anchor points covering the research surface. For optimization purposes, appropriate raw signal weighing was applied in accordance with previous research on the same data. The novel approach in this work consisted of performing a virtual tessellation of the considered indoor surface with a regular set of tiles encompassing the whole area. The optimization process was focused on varying the size of the tiles as well as their relative position concerning the signal acquisition grid, with the goal of minimizing the average distance error based on tile identification accuracy. The optimization process was conducted using a standard Quantum Particle Swarm Optimization (QPSO), while the position error estimate for each tile configuration was performed using a 3-layer Multilayer Perceptron (MLP) neural network. These experimental results showed a 16% reduction in the positioning error when a suitable tile configuration was calculated in the optimization process. Our final achieved value of 0.611 m of location incertitude shows a sensible improvement compared to our previous results. Full article
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<p>A sketch of the research area, with depictions of irregular boundaries, signal sources, and the grid of anchor points where signal intensities were recorded.</p>
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<p>(<b>left</b>) The layout of the anchor points (blue circles) and test points in random positions (black dots) within the experimental area. (<b>right</b>) A tessellation of the research area is shown, with respect to the anchor points.</p>
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<p>The profiles of the position error relative to the training and testing data in a typical MLP run. The minimum value in the test profile is highlighted.</p>
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<p>(<b>left</b>) The values of the horizontal and vertical contributions to the total positioning error, as calculated at each QPSO iteration. (<b>right</b>) The overall performance of the QPSO algorithm in terms of the positioning error reduction. A final value of 0.611 m was achieved.</p>
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13 pages, 3469 KiB  
Article
Finite Element Simulation Model of Metallic Thermal Conductivity Detectors for Compact Air Pollution Monitoring Devices
by Josée Mallah and Luigi G. Occhipinti
Sensors 2024, 24(14), 4683; https://doi.org/10.3390/s24144683 - 19 Jul 2024
Viewed by 2568
Abstract
Air pollution has been associated with several health problems. Detecting and measuring the concentration of harmful pollutants present in complex air mixtures has been a long-standing challenge, due to the intrinsic difficulty of distinguishing among these substances from interferent species and environmental conditions, [...] Read more.
Air pollution has been associated with several health problems. Detecting and measuring the concentration of harmful pollutants present in complex air mixtures has been a long-standing challenge, due to the intrinsic difficulty of distinguishing among these substances from interferent species and environmental conditions, both indoor and outdoor. Despite all efforts devoted by the scientific and industrial communities to tackling this challenge, the availability of suitable device technologies able to selectively discriminate these pollutants present in the air at minute, yet dangerous, concentrations and provide a quantitative measure of their concentrations is still an unmet need. Thermal conductivity detectors (TCDs) show promising characteristics that make them ideal gas sensing tools capable of recognising different gas analytes based on their physical fingerprint characteristics at the molecular level, such as their density, thermal conductivity, dynamic viscosity, and others. In this paper, the operation of TCD gas sensors is presented and explored using a finite element simulation of Joule heating in a sensing electrode placed in a gas volume. The results obtained show that the temperature, and hence, the resistance of the individual suspended microbridge sensor device, depends on the surrounding gas and its thermal conductivity, while the sensitivity and power consumption depend on the properties of the constitutive metal. Moreover, the electrode resistance is proven to be linearly dependent on the applied voltage. Full article
(This article belongs to the Section Electronic Sensors)
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<p>Full geometry of the electrode placed at the centre of the gas block (<b>left</b>)—the electrode is very small compared to the gas volume. Electrode-only zoom-in (<b>right</b>).</p>
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<p>Thermal conductivity (<b>a</b>,<b>d</b>,<b>g</b>), heat capacity at constant pressure (<b>b</b>,<b>e</b>,<b>h</b>), and density (<b>c</b>,<b>f</b>) of air (<b>a</b>–<b>c</b>), CO<sub>2</sub> (<b>d</b>–<b>f</b>), and NH<sub>3</sub> (<b>g</b>,<b>h</b>). NH<sub>3</sub> has a constant density of 0.73 kg/m<sup>3</sup> (not plotted).</p>
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<p>Temperature distribution in the electrode for the different metal–gas combinations at the last simulation time of 10 s. The metals used are Al (<b>a</b>–<b>c</b>), Au (<b>d</b>–<b>f</b>), and W (<b>g</b>–<b>i</b>) with respective input voltages of 0.17 V, 0.15 V, and 0.25 V, while the gases are NH<sub>3</sub> (<b>a</b>,<b>d</b>,<b>g</b>), air (<b>b</b>,<b>e</b>,<b>h</b>), and CO<sub>2</sub> (<b>c</b>,<b>f</b>,<b>i</b>).</p>
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<p>Graphs of the temperature at the centre of the electrode as a function of time with all 3 gases for Al (<b>a</b>), Au (<b>b</b>), and W (<b>c</b>).</p>
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<p>Thermal conductivity of air, NH<sub>3</sub>, and CO<sub>2</sub> as a function of temperature (data from COMSOL).</p>
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<p>Electrode resistance as a function of the input voltage in the presence of each of 3 gases (CO<sub>2</sub>, air, and NH<sub>3</sub>) for all 3 electrode materials (Al (<b>a</b>), Au (<b>b</b>), and W (<b>c</b>)).</p>
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<p>Electrode centre temperature as a function of the input potential for all 3 gases (CO<sub>2</sub>, air, and NH<sub>3</sub>) and electrode materials (Al (<b>a</b>), Au (<b>b</b>), and W (<b>c</b>)).</p>
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<p>Electrode centre temperature for Al (<b>a</b>–<b>c</b>), Au (<b>d</b>–<b>f</b>), and W (<b>g</b>–<b>i</b>) over 0.01 s (<b>a</b>,<b>d</b>,<b>g</b>), 0.2 ms (<b>b</b>,<b>e</b>,<b>h</b>), 0.04 ms (<b>c</b>,<b>f</b>,<b>i</b>) timeframes.</p>
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<p>Electrode centre temperature for Al (<b>a</b>–<b>c</b>), Au (<b>d</b>–<b>f</b>), and W (<b>g</b>–<b>i</b>) over 0.01 s (<b>a</b>,<b>d</b>,<b>g</b>), 0.2 ms (<b>b</b>,<b>e</b>,<b>h</b>), 0.04 ms (<b>c</b>,<b>f</b>,<b>i</b>) timeframes.</p>
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12 pages, 2102 KiB  
Article
Facile Preparation of TiO2NTs/Au@MOF Nanocomposites for High-Sensitivity SERS Sensing of Gaseous VOC
by Chunyan Wang, Yina Jiang, Yuyu Peng, Jia Huo and Ban Zhang
Sensors 2024, 24(14), 4447; https://doi.org/10.3390/s24144447 - 10 Jul 2024
Viewed by 1018
Abstract
Surface-enhanced Raman spectroscopy (SERS) is a promising and highly sensitive molecular fingerprint detection technology. However, the development of SERS nanocomposites that are label-free, highly sensitive, selective, stable, and reusable for gaseous volatile organic compounds (VOCs) detection remains a challenge. Here, we report a [...] Read more.
Surface-enhanced Raman spectroscopy (SERS) is a promising and highly sensitive molecular fingerprint detection technology. However, the development of SERS nanocomposites that are label-free, highly sensitive, selective, stable, and reusable for gaseous volatile organic compounds (VOCs) detection remains a challenge. Here, we report a novel TiO2NTs/AuNPs@ZIF−8 nanocomposite for the ultrasensitive SERS detection of VOCs. The three-dimensional TiO2 nanotube structure with a large specific surface area provides abundant sites for the loading of Au NPs, which possess excellent local surface plasmon resonance (LSPR) effects, further leading to the formation of a large number of SERS active hotspots. The externally wrapped porous MOF structure adsorbs more gaseous VOC molecules onto the noble metal surface. Under the synergistic mechanism of physical and chemical enhancement, a better SERS enhancement effect can be achieved. By optimizing experimental conditions, the SERS detection limit for acetophenone, a common exhaled VOC, is as low as 10−11 M. And the relative standard deviation of SERS signal intensity from different points on the same nanocomposite surface is 4.7%. The acetophenone gas achieves a 1 min response and the signal reaches stability in 4 min. Under UV irradiation, the surface-adsorbed acetophenone can be completely degraded within 40 min. The experimental results demonstrate that this nanocomposite has good detection sensitivity, repeatability, selectivity, response speed, and reusability, making it a promising sensor for gaseous VOCs. Full article
(This article belongs to the Section Biosensors)
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<p>SEM images of TiO<sub>2</sub>NTs/AuNPs (<b>a</b>) and TiO<sub>2</sub>NTs/AuNPs@ZIF−8 nanocomposites obtained at 30 min (<b>b</b>); EDS element distribution map (<b>c</b>) and Spectrum (<b>d</b>) of TiO<sub>2</sub>NTs/AuNPs@ZIF−8.</p>
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<p>SEM image of TiO<sub>2</sub>NTs/AuNPs@ZIF−8 nanocomposites obtained at three different deposition times: 15 min (<b>a</b>), 30 min (<b>b</b>), and 45 min (<b>c</b>), respectively.</p>
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<p>(<b>a</b>) The SERS spectra of 1 ppm gaseous acetophenone adsorbed on the surface of TiO<sub>2</sub>NTs/AuNPs@ZIF−8 nanocomposites with different ZIF−8 shell thicknesses for 30 min; (<b>b</b>) SERS spectra of 1 ppb gaseous acetophenone adsorbed on TiO<sub>2</sub>NTs/AuNPs@ZIF−8 nanocomposites with ZIF−8 shell thickness of 6 nm for different times.</p>
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<p>(<b>a</b>) SERS spectra of different concentrations of acetophenone on the surface of the TiO<sub>2</sub>NTs/AuNPs@ZIF−8 nanocomposites. Inner picture is the plot of the intensity of SERS peak at 1025 cm<sup>−1</sup> versus the logarithm of acetone concentration. (<b>b</b>) SERES spectra measured at 20 different spots on the surface of the TiO<sub>2</sub>NTs/AuNPs@ZIF−8 nanocomposites adsorbed with acetophenone (color insert shows Raman mapping of the substrate surface at 20 different points). The electromagnetic simulation diagrams of the TiO<sub>2</sub>NTs/AuNPs@ZIF−8 composite nanostructure: (<b>c</b>) top view; (<b>d</b>) front view.</p>
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<p>(<b>a</b>) SERS spectra of different concentrations of acetophenone on the surface of the TiO<sub>2</sub>NTs/AuNPs@ZIF−8 nanocomposites. Inner picture is the plot of the intensity of SERS peak at 1025 cm<sup>−1</sup> versus the logarithm of acetone concentration. (<b>b</b>) SERES spectra measured at 20 different spots on the surface of the TiO<sub>2</sub>NTs/AuNPs@ZIF−8 nanocomposites adsorbed with acetophenone (color insert shows Raman mapping of the substrate surface at 20 different points). The electromagnetic simulation diagrams of the TiO<sub>2</sub>NTs/AuNPs@ZIF−8 composite nanostructure: (<b>c</b>) top view; (<b>d</b>) front view.</p>
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<p>(<b>a</b>) The SERS spectra of three common exhaled VOCs and their mixtures, adsorbed on the surface of the nanocomposites, respectively. (<b>b</b>) SERS spectra of 10<sup>−7</sup> M acetophenone on the TiO<sub>2</sub>NTs/AuNPs@ZIF−8 surface under UV light irradiation at different times.</p>
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14 pages, 7264 KiB  
Article
Organic-Acid-Sensitive Visual Sensor Array Based on Fenton Reagent–Phenol/Aniline for the Rapid Species and Adulteration Assessment of Baijiu
by Lei Zhang, Yaqi Liu, Zhenli Cai, Meixia Wu and Yao Fan
Foods 2024, 13(13), 2139; https://doi.org/10.3390/foods13132139 - 5 Jul 2024
Viewed by 997
Abstract
Baijiu is an ancient, distilled spirit with a complicated brewing process, unique taste, and rich trace components. These trace components play a decisive role in the aroma, taste, and especially the quality of baijiu. In this paper, the redox reaction between the Fenton [...] Read more.
Baijiu is an ancient, distilled spirit with a complicated brewing process, unique taste, and rich trace components. These trace components play a decisive role in the aroma, taste, and especially the quality of baijiu. In this paper, the redox reaction between the Fenton reagent and four reducing agents, including o-phenylenediamine (OPD), p-phenylenediamine (PPD), 4-aminophenol (PAP), and 2-aminophenol (OAP), was adopted to construct a four-channel visual sensor array for the rapid detection of nine kinds of common organic acids in baijiu and the identification of baijiu and its adulteration. By exploiting the color-changing fingerprint response brought by organic acids, each organic acid could be analyzed accurately when combined with an optimized variable-weighted least-squares support vector machine based on a particle swarm optimization (PSO-VWLS-SVM) model. What is more, this novel sensor also could achieve accurate semi-quantitative analysis of the mixed organic acid samples via partial least squares discriminant analysis (PLSDA). Most importantly, the sensor array could be further used for the identification of baijiu with different species through the PLSDA model and the adulteration assessment with the one-class partial least squares (OCPLS) model simultaneously. Full article
(This article belongs to the Section Food Analytical Methods)
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<p>Effect of ethanol on organic-acid-sensitive Fenton reagent–phenol/aniline visual sensor array.</p>
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<p>Comparison of color results under different concentrations of reactants.</p>
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<p>Comparison of the color results of the reaction at different times.</p>
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<p>Organic-acid-sensitive Fenton reagent–phenol/aniline visual sensor array with different concentrations of organic acids added: benzoic acid (<b>A1</b>); lactic acid (<b>A2</b>); acetic acid (<b>A3</b>); butyric acid (<b>A4</b>); isobutyric acid (<b>A5</b>); valeric acid (<b>A6</b>); isovaleric acid (<b>A7</b>); hexanoic acid (<b>A8</b>); octanoic acid (<b>A9</b>).</p>
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<p>The pattern recognition results of mixed organic acids based on four-channel colorimetric sensor array via PLSDA.</p>
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<p>(<b>A</b>) The colorimetric results of the organic-acid-sensitive Fenton reagent–phenol/aniline visual sensor array for nine organic acids (25 mmol/L) in the presence of acetaldehyde (25 mmol/L) and ethyl caproate (25 mmol/L); (<b>B</b>) the colorimetric results of the sensor array for nine organic acids in the absence of interferences; (<b>C</b>) the color difference of the colorimetric results in the presence and absence of interference substances.</p>
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<p>Recognition of 12 different baijiu samples with various aroma types (<b>A</b>) and species (<b>B</b>) via organic-acid-sensitive Fenton reagent–phenol/aniline visual sensor array through PLSDA.</p>
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<p>Adulteration assessment of baijiu samples via OCPLS: (<b>a</b>) the result for training samples; (<b>b</b>) the result for prediction samples; (<b>c</b>) the enlarged view of the regular point region in the result for prediction samples.</p>
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<p>Illustration of organic-acid-sensitive Fenton reagent–phenol/aniline visual sensor array.</p>
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14 pages, 6723 KiB  
Article
A Novel Terahertz Metamaterial Microfluidic Sensing Chip for Ultra-Sensitive Detection
by Yuan Zhang, Keke Jia, Hongyi Ge, Xiaodi Ji, Yuying Jiang, Yuwei Bu, Yujie Zhang and Qingcheng Sun
Nanomaterials 2024, 14(13), 1150; https://doi.org/10.3390/nano14131150 - 4 Jul 2024
Viewed by 1291
Abstract
A terahertz metamaterial microfluidic sensing chip for ultrasensitive detection is proposed to investigate the response of substances to terahertz radiation in liquid environments and enhance the molecular fingerprinting of trace substances. The structure consists of a cover layer, a metal microstructure, a microfluidic [...] Read more.
A terahertz metamaterial microfluidic sensing chip for ultrasensitive detection is proposed to investigate the response of substances to terahertz radiation in liquid environments and enhance the molecular fingerprinting of trace substances. The structure consists of a cover layer, a metal microstructure, a microfluidic channel, a metal reflective layer, and a buffer layer from top to bottom, respectively. The simulation results show that there are three obvious resonance absorption peaks in the range of 1.5–3.0 THz and the absorption intensities are all above 90%. Among them, the absorption intensity at M1 = 1.971 THz is 99.99%, which is close to the perfect absorption, and its refractive index sensitivity and Q-factor are 859 GHz/RIU and 23, respectively, showing excellent sensing characteristics. In addition, impedance matching and equivalent circuit theory are introduced in this paper to further analyze the physical mechanism of the sensor. Finally, we perform numerical simulations using refractive index data of normal and cancer cells, and the results show that the sensor can distinguish different types of cells well. The chip can reduce the sample pretreatment time as well as enhance the interaction between terahertz waves and matter, which can be used for early disease screening and food quality and safety detection in the future. Full article
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<p>(<b>a</b>) TMMSC under TE-polarized terahertz wave irradiation. (<b>b</b>) Metallic microstructure. (<b>c</b>) Structural design diagram of microfluidic sensor based on the particle swarm optimization algorithm.</p>
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<p>(<b>a</b>) TMMSC characteristic absorption curve. (<b>b</b>) the relative impedance of TMMSC in M1. (<b>c</b>) RLC equivalent circuit model. (<b>d</b>) Simulated absorption from ADS and CST.</p>
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<p>(<b>a</b>) TMMSC characteristic absorption curve. (<b>b</b>) the relative impedance of TMMSC in M1. (<b>c</b>) RLC equivalent circuit model. (<b>d</b>) Simulated absorption from ADS and CST.</p>
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<p>Electric field along the z-plane and surface current distribution for a sample-free resonance in the TMMSC microfluidic channel. (<b>a</b>) Re(Ez) of M1, (<b>b</b>) Re(Ez) of M2, (<b>c</b>) Re(Ez) of M3, (<b>d</b>) surface current of M1, (<b>e</b>) surface current of M2, and (<b>f</b>) surface current of M3 resonance peaks.</p>
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<p>(<b>a</b>) Absorption characteristics of TE and TM polarized THz waves. (<b>b</b>) TM polarized electric field distribution.</p>
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<p>(<b>a</b>) Variation of absorption with phi for theta = 0°. (<b>b</b>) Variation of absorption with theta for phi = 0°.</p>
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<p>(<b>a</b>) TMMS absorption characteristics for different h2; (<b>b</b>) variation of Q-factor and absorption intensity of M1 with h2. (<b>c</b>) TMMS absorption characteristics for different r; (<b>d</b>) variation of Q-factor and absorption intensity of M1 with r. (<b>e</b>) TMMS absorption characteristics for different w; (<b>f</b>) variation of Q-factor and absorption intensity of M1 with w.</p>
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<p>(<b>a</b>) Absorption curves with and without sample filling in the microfluidic channel. (<b>b</b>) Absorption and Q-factor of M1 and M2 resonance peaks. (<b>c</b>) The detection capability of PI-type sensor. (<b>d</b>) The detection capability of quartz-type sensor. (<b>e</b>) The frequency shift of the M1 resonance peak. (<b>f</b>) Sensitivity and FOM of M1 resonance peak.</p>
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<p>(<b>a</b>) Absorption curve of TMMSC when filling cancer and normal cells. (<b>b</b>) Frequency shift relationship curve.</p>
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<p>Process flow including (1) photolithography and etching to form microcirculation channels in the buffer layer; (2) production of metallic reflective layers; (3) creating a metal resonance pattern on a cover plate; (4) punching of holes in the cover plate; (5) bonding of the silicon substrate and the cover plate for encapsulation.</p>
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17 pages, 2986 KiB  
Article
Simple Siamese Model with Long Short-Term Memory for User Authentication with Field-Programmable Gate Arrays
by Hyun-Sik Choi
Electronics 2024, 13(13), 2584; https://doi.org/10.3390/electronics13132584 - 1 Jul 2024
Cited by 1 | Viewed by 691
Abstract
Recent studies have focused on user authentication methods that use biometric signals such as electrocardiogram (ECG) and photo-plethysmography (PPG). These authentication technologies have advantages such as ease of acquisition, strong security, and the capability for non-aware authentication. This study addresses user authentication using [...] Read more.
Recent studies have focused on user authentication methods that use biometric signals such as electrocardiogram (ECG) and photo-plethysmography (PPG). These authentication technologies have advantages such as ease of acquisition, strong security, and the capability for non-aware authentication. This study addresses user authentication using electromyogram (EMG) signals, which are particularly easy to acquire, can be fabricated in a wearable form such as a wristwatch, and are readily expandable with technologies such as human–machine interface. However, despite their potential, they often exhibit lower accuracy (approximately 90%) than traditional methods such as fingerprint recognition. Accuracy can be improved using complex algorithms and multiple biometric authentication technologies; however, complex algorithms use substantial hardware resources, making their application to wearable devices difficult. In this study, a simple Siamese model with long short-term memory (LSTM) (SSiamese-LSTM) is proposed to achieve a high accuracy of over 99% with limited resources suitable for wearable devices. The hardware implementation was accomplished using field-programmable gate arrays (FPGAs). In terms of accuracy, EMG measurement results from Chosun University were used, and data from 100 individuals were employed for verification. The proposed digital logic will be integrated with an EMG sensor in the form of a watch that can be used for user authentication. Full article
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<p>EMD signal analysis. (<b>a</b>) Original signal (A), (<b>b</b>) Original signal (B), (<b>c</b>) IMF<sub>1</sub> (A), (<b>d</b>) IMF<sub>1</sub> (B), (<b>e</b>) IMF<sub>4</sub> (A), and (<b>f</b>) IMF<sub>4</sub> (B). A and B refer to different individuals.</p>
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<p>Structure of the proposed SSiamese neural networks for embeddings.</p>
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<p>Simple schematic of LSTM blocks.</p>
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<p>Confusion matrix for user authentication.</p>
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<p>ROC curve for user authentication. The dashed line represents the performance of a random classifier.</p>
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<p>Bit precision of parameters used in each layer by Keras and implemented in hardware.</p>
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<p>Schematic diagram of the proposed user authentication system implemented in the form of a wearable watch.</p>
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14 pages, 6445 KiB  
Article
Multi-Sensor-Assisted Low-Cost Indoor Non-Visual Semantic Map Construction and Localization for Modern Vehicles
by Guangxiao Shao, Fanyu Lin, Chao Li, Wei Shao, Wennan Chai, Xiaorui Xu, Mingyue Zhang, Zhen Sun and Qingdang Li
Sensors 2024, 24(13), 4263; https://doi.org/10.3390/s24134263 - 30 Jun 2024
Viewed by 1062
Abstract
With the transformation and development of the automotive industry, low-cost and seamless indoor and outdoor positioning has become a research hotspot for modern vehicles equipped with in-vehicle infotainment systems, Internet of Vehicles, or other intelligent systems (such as Telematics Box, Autopilot, etc.). This [...] Read more.
With the transformation and development of the automotive industry, low-cost and seamless indoor and outdoor positioning has become a research hotspot for modern vehicles equipped with in-vehicle infotainment systems, Internet of Vehicles, or other intelligent systems (such as Telematics Box, Autopilot, etc.). This paper analyzes modern vehicles in different configurations and proposes a low-cost, versatile indoor non-visual semantic mapping and localization solution based on low-cost sensors. Firstly, the sliding window-based semantic landmark detection method is designed to identify non-visual semantic landmarks (e.g., entrance/exit, ramp entrance/exit, road node). Then, we construct an indoor non-visual semantic map that includes the vehicle trajectory waypoints, non-visual semantic landmarks, and Wi-Fi fingerprints of RSS features. Furthermore, to estimate the position of modern vehicles in the constructed semantic maps, we proposed a graph-optimized localization method based on landmark matching that exploits the correlation between non-visual semantic landmarks. Finally, field experiments are conducted in two shopping mall scenes with different underground parking layouts to verify the proposed non-visual semantic mapping and localization method. The results show that the proposed method achieves a high accuracy of 98.1% in non-visual semantic landmark detection and a low localization error of 1.31 m. Full article
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<p>An illustration of the proposed system structure. I. Non-visual semantic detection, II. map construction, and III. matching and localization (the black, red and cyan dots represent the waypoint, non-visual semantic Landmark and Wi-Fi fingerprint, and the green lines represent the matching relationship of non-visual semantics between the venue map and the trajectory map).</p>
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<p>Diagram of joint points.</p>
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<p>The diagram of the road node’s features in a sliding window (the blue dashed line is the auxiliary line).</p>
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<p>The association relationship among the waypoints, non-visual semantic landmarks, and Wi-Fi fingerprints in a single-trajectory semantic map.</p>
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<p>A schematic diagram of the experimental scene. (<b>a</b>) is a schematic of the floor B3 in the mall 1 scene and (<b>b</b>) is a schematic of the floor B4 in the mall 2 scene.</p>
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<p>Non-visual semantic landmark matching results between the trajectory map and the venue map in two mall scenes. (<b>a</b>,<b>b</b>) represent the results of non-visual semantic landmark matching in mall 1 and mall 2. Red star represents road node, green and red triangle represent slop entry/exit, green and red square represent entry/exit. Black line indicates the waypoints of the constructed scene map, the blue line indicates the waypoints of the new localization map, and the cyan line represent the matching relationship of non-visual semantics between the venue map and the new localization map.</p>
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<p>The localization results based on non-visual semantic landmark matching. (<b>a</b>,<b>b</b>) represents a schematic diagram of 2D and 3D localization results in mall 1. (<b>c</b>,<b>d</b>) represents a schematic diagram of 2D and 3D localization results in mall 2. The blue line indicates the constructed scene map, and the green line indicates the new localization map.</p>
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<p>CDF of localization errors of two malls. (<b>a</b>) is CDF of location errors of mall 1 scene, and (<b>b</b>) is CDF of location errors of mall 2 scene.</p>
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