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Search Results (31,164)

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31 pages, 12897 KiB  
Article
Poly (Lactic Acid) Fibrous Film with Betalains from Pitaya (Stenocereus thurberi) by Electrospinning for Potential Use as Smart Food Packaging
by Dalila Fernanda Canizales-Rodríguez, Francisco Rodríguez-Félix, José Agustín Tapia-Hernández, Carmen Lizette Del-Toro-Sánchez, Saúl Ruíz-Cruz, Santiago P. Abourg, Victor Manuel Ocaño-Higuera, María Irene Silvas-García, Cielo Estefanía Figueroa-Enríquez and Milagros Guadalupe Álvarez-Moreno
Coatings 2024, 14(12), 1581; https://doi.org/10.3390/coatings14121581 (registering DOI) - 18 Dec 2024
Abstract
The incorporation of biopolymers and natural colorants in smart packaging has garnered significant attention in the food packaging industry. This study investigates the design and characterization of novel fibrous films incorporating betalain extract (BE) from Stenocereus thurberi in poly (lactic acid) (PLA). An [...] Read more.
The incorporation of biopolymers and natural colorants in smart packaging has garnered significant attention in the food packaging industry. This study investigates the design and characterization of novel fibrous films incorporating betalain extract (BE) from Stenocereus thurberi in poly (lactic acid) (PLA). An electrospinning technique was developed with varying PLA concentrations (2%–12% w/v) and BE concentrations (8%–12% w/v) to create a colorimetric freshness indicator. BE was characterized by quantifying its phytochemical content and assessing its antioxidant capacity. Morphological and structural analyses included scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), polydispersity index (PI), mechanical properties, and functional characteristics such as ammonia sensitivity and total antioxidant activity. The results indicated that the incorporation of BE significantly influenced the average diameter of the nanofibers, ranging from 313 ± 74 nm to 657 ± 99 nm. SEM micrographs showed that PLA12-BE12 films exhibited smooth surfaces without bead formation. The FTIR analysis confirmed effective BE incorporation, revealing intermolecular interactions between the betalain molecules and the PLA matrix, which contributed to enhanced structural and functional stability. The mechanical properties analysis revealed that moderate BE additions (8%–10% w/v) enhanced the Young’s modulus and tensile strength, while higher BE concentrations (12% w/v) disrupted the polymer network, reducing these properties. Additionally, the strain at break decreased significantly with BE incorporation, reflecting limited molecular chain mobility. Increasing BE concentration notably improved antioxidant activity, with the BE concentration of 12% (w/v), the ABTS•+, DPPH•, and FRAP radical scavenging activities at the highest values of 84.28 ± 1.59%, 29.95 ± 0.34%, and 710.57 ± 28.90 µM ET/g, respectively. Ammonia sensitivity tests demonstrated a significant halochromic transition from reddish-pink to yellow, indicating high sensitivity to low ammonia concentrations. The possible mechanism is alkaline pH induces aldimine bond hydrolysis and generates betalamic acid (yellow) and cyclo-DOPA-5-O-ß-glucoside (colorless) The fibrous films also exhibited reversible color changes and maintained good color stability over 30 days, emphasizing their potential for use in smart packaging applications for real-time freshness monitoring and food quality assessment. Full article
(This article belongs to the Special Issue Novel Advances in Food Contact Materials)
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Figure 1

Figure 1
<p>Schematic diagram of the production of PLA12-BE12 nanofibrous film by electrospinning technique.</p>
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<p>UV-vis spectra (<b>a</b>,<b>b</b>) and photograph of color variations (<b>c</b>) in pH 1–14 range of betalain solutions.</p>
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<p>SEM micrographs of PLA films at 2 (<b>a</b>), 4 (<b>b</b>), 6 (<b>c</b>), 8 (<b>d</b>), 10 (<b>e</b>), and 12 (<b>f</b>) % (<span class="html-italic">w</span>/<span class="html-italic">v</span>) fiber. Magnifications images are 1000× and 5000×. Yellow circles show fibers defects.</p>
Full article ">Figure 4
<p>SEM micrographs of PLA 8, 10, and 12% (<span class="html-italic">w</span>/<span class="html-italic">v</span>) fibrous film incorporated with BE at 8% (<span class="html-italic">w</span>/<span class="html-italic">v</span>). The magnification images are 1000× and 5000×. Yellow circles show fibers defects.</p>
Full article ">Figure 5
<p>SEM micrographs of PLA 8, 10, and 12% (<span class="html-italic">w</span>/<span class="html-italic">v</span>) film incorporated with BE at 10% (<span class="html-italic">w</span>/<span class="html-italic">v</span>). The magnification images are 1000× and 5000×. Yellow circles show fibers defects.</p>
Full article ">Figure 6
<p>SEM micrographs of PLA 8, 10, and 12% (<span class="html-italic">w</span>/<span class="html-italic">v</span>) fibrous films incorporated with BE at 12% (<span class="html-italic">w</span>/<span class="html-italic">v</span>). The magnification images are 1000× and 5000×. Yellow circles show fibers defects.</p>
Full article ">Figure 7
<p>SEM micrographs of PLA 12% (<b>a</b>), PLA12%-BE8% (<b>b</b>), PLA12%-BE10% (<b>c</b>), and PA12%-BE12% (<b>d</b>) (<span class="html-italic">w</span>/<span class="html-italic">v</span>) fibrous films and their corresponding histograms. The magnification images are 5000×.</p>
Full article ">Figure 8
<p>Physical appearance and color value (<span class="html-italic">L</span>, <span class="html-italic">a</span>*, <span class="html-italic">b</span>* and Δ<span class="html-italic">E</span>) of PLA 8, 10, and 12% (<span class="html-italic">w</span>/<span class="html-italic">v</span>) fibrous films with the addition of BE at 8, 10, and 12% (<span class="html-italic">w</span>/<span class="html-italic">v</span>).</p>
Full article ">Figure 9
<p>FTIR spectra of the fibrous film: PLA 12% (<b>a</b>), BE (<b>b</b>), PLA12-BE12 (<b>c</b>).</p>
Full article ">Figure 10
<p>Color response of PLA12-BET12 indicator fibrous film at different ammonia concentrations: photographs after reaction with ammonia (<b>a</b>) and color values of the film after reaction with ammonia (Δ<span class="html-italic">E</span>, Δ<span class="html-italic">L</span>, Δ<span class="html-italic">a</span>, Δ<span class="html-italic">b</span>) (<b>b</b>) at 10 min of reaction. Data with different letters on the same column color refer to significant differences (<span class="html-italic">p</span> &lt; 0.05). Data (mean ± SD) are from three independent experiments.</p>
Full article ">Figure 11
<p>Color response of PLA12-BE12 fibrous film, at different ammonia concentrations: photographs after reaction with ammonia (<b>a</b>), color values of the film after reaction with ammonia (Δ<span class="html-italic">E</span>, Δ<span class="html-italic">L</span>, Δ<span class="html-italic">a</span>, Δ<span class="html-italic">b</span>) (<b>b</b>), at 20 min of reaction. Data with different letters on the same column color reference to significant differences (<span class="html-italic">p</span> &lt; 0.05). Data (mean ± SD) are from three independent experiments.</p>
Full article ">Figure 12
<p>ABTS•+ radical inhibition (<b>a</b>), DPPH• radical inhibition (<b>b</b>), and FRAP µM TE/g (<b>c</b>) of different fibrous films at various immersion times. Data (mean ± SD) are from three independent experiments.</p>
Full article ">Figure 13
<p>Color responses of PLA12-BE12 fibrous film after reaction during four cycles in extremely acidic and alkaline atmospheres.</p>
Full article ">Figure 14
<p>Total color change (Δ<span class="html-italic">E</span>) for PLA12-BE12 fibrous film during storage at 4 °C and 25 °C at 30 days. Data with different letters on the same column color refer to significant differences (<span class="html-italic">p</span> &lt; 0.05). Data (mean ± SD) are from three independent experiments.</p>
Full article ">Figure 15
<p>Photograph of PLA12-BE12 intelligent fibrous film indicator during storage at 4 °C and 25 °C at 30 days.</p>
Full article ">Figure 16
<p>Hue angles of the intelligent fibrous film indicator during storage at 4 °C and 25 °C at 30 days. Data with different letters on the same column color refer to significant differences (<span class="html-italic">p</span> &lt; 0.05). Data (mean ± SD) are from three independent experiments.</p>
Full article ">Figure 17
<p>Chroma values of the indicator fibrous film during storage at 4 °C and 25 °C at 30 days. Data with different letters on the same column color refer to significant differences (<span class="html-italic">p</span> &lt; 0.05). Data (mean ± SD) are from three independent experiments.</p>
Full article ">
17 pages, 1626 KiB  
Article
Multiple Electromechanical-Failure Detection in Induction Motor Using Thermographic Intensity Profile and Artificial Neural Network
by Emmanuel Resendiz-Ochoa, Salvador Calderon-Uribe, Luis A. Morales-Hernandez, Carlos A. Perez-Ramirez and Irving A. Cruz-Albarran
Machines 2024, 12(12), 928; https://doi.org/10.3390/machines12120928 (registering DOI) - 17 Dec 2024
Abstract
The use of artificial intelligence-based techniques to solve engineering problems is increasing. One of the most challenging tasks facing industry is the timely diagnosis of failures in electromechanical systems, as they are an essential part of production systems. In this sense, the earlier [...] Read more.
The use of artificial intelligence-based techniques to solve engineering problems is increasing. One of the most challenging tasks facing industry is the timely diagnosis of failures in electromechanical systems, as they are an essential part of production systems. In this sense, the earlier the detection, the higher the economic loss reduction. For this reason, this work proposes the development of a new methodology based on infrared thermography and an artificial intelligence-based classifier for the detection of multiple faults in an electromechanical system. The proposal combines the intensity profile of the grey-scale image, the use of Fast Fourier Transform and an artificial neural network to perform the detection of twelve states for the state of an electromechanical system: healthy, bearing defect, broken rotor bar, misalignment and gear wear on the gearbox. From the experimental setup, 50 thermographic images were obtained for each state. The method was implemented and tested under different conditions to verify its reliability. The results show that the precision, accuracy, recall and F1-score are higher than 99%. Thus, it can be concluded that it is possible to detect multiple conditions in an electromechanical system using the intensity profile and an artificial neural network, achieving good accuracy and reliability. Full article
20 pages, 28423 KiB  
Article
Optical–Physical Characteristics of Low Clouds and Aerosols in South America Based on Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation
by Bo Su, Dekai Lin, Ziji Liu, Qingyan Wu, Wenkai Song and Miao Zhang
Atmosphere 2024, 15(12), 1513; https://doi.org/10.3390/atmos15121513 (registering DOI) - 17 Dec 2024
Abstract
Clouds and aerosols, as important factors in the Earth’s climate system, have significant impacts on the atmospheric environment and global climate. This study investigated the optical and physical properties of clouds and aerosols over South America from 2006 to 2021 using CALIPSO Level [...] Read more.
Clouds and aerosols, as important factors in the Earth’s climate system, have significant impacts on the atmospheric environment and global climate. This study investigated the optical and physical properties of clouds and aerosols over South America from 2006 to 2021 using CALIPSO Level 2 products. South America was divided into four regions: A (Western Andean Mountains), B (Northern Orinoco and Amazon plains), C (Southern La Plata Plains), and D (Eastern Brazilian Highlands). Seasonal variations in the optical properties of low clouds and their interactions with the lowest-layer aerosols were analyzed and compared. The results indicate that Region C had the highest OPlc (probability of low clouds) and AODlc (AOD (Aerosol Optical Depth) of low clouds, likely due to its flat terrain and westerly influences. Both AODlc and OPlc were higher in September–November compared to other seasons. DRlc (depolarization ratio of low clouds) values were higher in Regions C and D, particularly in September–February, possibly due to topographic effects and more precipitation and higher humidity during this period. The elevated CRlc (color ratio of low clouds) in Region A may be attributed to the Andes blocking warm, moist air, leading to increased precipitation and cloud particle content. HLlc (top height of low clouds) and BLlc (base altitude of low clouds) were positively correlated with geographic elevation, while Tlc (thickness of low clouds) was greater at night, potentially due to enhanced atmospheric stability. Furthermore, strong correlations among certain parameters suggested significant interactions between aerosols and clouds. Full article
(This article belongs to the Section Atmospheric Techniques, Instruments, and Modeling)
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Figure 1

Figure 1
<p>The geographical location and zoning of South America. The color bar represents the altitude (elevation). Divided into four regions: A, B, C, and D.</p>
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<p>Seasonal spatial distribution of probability of occurrence of low clouds (OP<sub>lc</sub>), AOD of low clouds (AOD<sub>lc</sub>), percentage of AOD for low clouds (PAOD<sub>lc</sub>), and depolarization ratio of low clouds (DR<sub>lc</sub>) over South America during the day.</p>
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<p>Seasonal spatial distributions of OP<sub>lc</sub>, AOD<sub>lc</sub>, PAOD<sub>lc</sub>, and DR<sub>lc</sub> over South America at night.</p>
Full article ">Figure 4
<p>Seasonal variation of AOD<sub>lc</sub>, PAOD<sub>lc</sub>, and DR<sub>lc</sub> over South America during the day and at night ((<b>a</b>) AOD<sub>lc</sub> daytime; (<b>b</b>) PAOD<sub>lc</sub> daytime; (<b>c</b>) DR<sub>lc</sub> daytime; (<b>d</b>) AOD<sub>lc</sub> nighttime; (<b>e</b>) PAOD<sub>lc</sub> nighttime; (<b>f</b>) DR<sub>lc</sub> nighttime).</p>
Full article ">Figure 5
<p>Seasonal spatial distributions of the probability of color ratio of low clouds (CR<sub>lc</sub>), base altitude of low clouds (B<sub>lc</sub>), top height of low clouds (H<sub>lc</sub>), and thickness of low clouds (T<sub>lc</sub>) over South America during the day.</p>
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<p>Seasonal spatial distributions of CR<sub>lc</sub>, B<sub>lc</sub>, H<sub>lc</sub>, and T<sub>lc</sub> over South America at night.</p>
Full article ">Figure 7
<p>Seasonal variation in CR<sub>lc</sub>, B<sub>lc</sub>, H<sub>lc</sub>, and T<sub>lc</sub> over South America during the day and at night ((<b>a</b>) CR<sub>lc</sub> daytime; (<b>b</b>) B<sub>lc</sub> daytime; (<b>c</b>) H<sub>lc</sub> daytime; (<b>d</b>) T<sub>lc</sub> nighttime; (<b>e</b>) CR<sub>lc</sub> nighttime; (<b>f</b>) B<sub>lc</sub> nighttime; (<b>g</b>) H<sub>lc</sub> nighttime; (<b>h</b>) T<sub>lc</sub> nighttime).</p>
Full article ">Figure 8
<p>Correlation of PAOD<sub>lc</sub> and AOD<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 9
<p>Correlation of Tlc and Hlc over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 10
<p>Correlation of B<sub>lc</sub> and H<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) winter daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 11
<p>Correlation of B<sub>lc</sub> and DR<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 12
<p>Correlation of AODR<sub>lc</sub> and DR<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 13
<p>Correlation of PAODR<sub>lc</sub> and DR<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 14
<p>Correlation of B<sub>la</sub> and B<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 15
<p>Correlation of H<sub>la</sub> and H<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 16
<p>Correlation of T<sub>la</sub> and T<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">Figure 17
<p>Correlation of PAOD<sub>la</sub> and PAOD<sub>lc</sub> over South America from 2006 to 2021: (<b>a</b>) MMA daytime; (<b>b</b>) JJA daytime; (<b>c</b>) SON daytime; (<b>d</b>) DJF nighttime; (<b>e</b>) MMA nighttime; (<b>f</b>) JJA nighttime; (<b>g</b>) SON nighttime; (<b>h</b>) DJF nighttime.</p>
Full article ">
17 pages, 6437 KiB  
Article
Application of Infrared Thermography in Identifying Plant Oils
by Maria Marudova, Sotir Sotirov, Nadezhda Kafadarova and Ginka Antova
Foods 2024, 13(24), 4090; https://doi.org/10.3390/foods13244090 (registering DOI) - 17 Dec 2024
Abstract
In this article, we present a unique system for identifying edible oils through the analysis of their thermophysical properties. The method is based on the use of active infrared thermography. The heating of the oils results from the optical absorption of laser radiation [...] Read more.
In this article, we present a unique system for identifying edible oils through the analysis of their thermophysical properties. The method is based on the use of active infrared thermography. The heating of the oils results from the optical absorption of laser radiation at a specified wavelength. This approach enables greater selectivity in differentiating between various types of edible oils, as the results depend not only on the thermal properties of the specific oils but also on their optical properties, which are uniquely characteristic of each oil. Additionally, the developed system provides a detailed visualization of spatial temperature gradients within the sample’s volume, as well as their changes over time. It overcomes the limitations of other methods that determine only the thermal conductivity coefficients of oils through resistive heating of the sample. In this article, four types of vegetable oils (extra virgin olive oil, sesame oil, sunflower oil, and rapeseed oil) have been studied. Fatty acid analysis, differential scanning calorimetry, and UV-VIS spectroscopy have been used to determine the authenticity, moisture content, and optical properties of the studied samples. The developed system allows for the visualization and determination of the emerging temperature gradients in the sample volume. Full article
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Figure 1

Figure 1
<p>The block diagram of the system for vegetable oils’ identification.</p>
Full article ">Figure 2
<p>Thermogram taken after the completion of the sample tempering process. (<b>a</b>) Thermogram of the sample before the measurement process; (<b>b</b>) temperature distribution profile along the longitudinal axis of the cuvette, shown as the blue line in (<b>a</b>).</p>
Full article ">Figure 3
<p>Crystallization and melting transitions of (<b>a</b>) SFO, (<b>b</b>) SO, (<b>c</b>) EVOO, and (<b>d</b>) RSO.</p>
Full article ">Figure 3 Cont.
<p>Crystallization and melting transitions of (<b>a</b>) SFO, (<b>b</b>) SO, (<b>c</b>) EVOO, and (<b>d</b>) RSO.</p>
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<p>UV-VIS spectra of EVOO, SO, RSO, and SFO.</p>
Full article ">Figure 5
<p>The obtained thermograms captured at (<b>a</b>) 20 s, (<b>b</b>) 80 s, and (<b>c</b>) 160 s from the study of extra virgin olive oil.</p>
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<p>The obtained thermograms captured at (<b>a</b>) 20 s, (<b>b</b>) 80 s, and (<b>c</b>) 160 s from the study of rapeseed oil.</p>
Full article ">Figure 7
<p>The obtained thermograms captured at (<b>a</b>) 20 s, (<b>b</b>) 80 s, and (<b>c</b>) 160 s from the study of sesame oil.</p>
Full article ">Figure 8
<p>The obtained thermograms captured at (<b>a</b>) 20 s, (<b>b</b>) 80 s, and (<b>c</b>) 160 s from the study of sunflower oil.</p>
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<p>Measured temperature profiles of 5 samples of olive oil at the 20th s after the start of the analysis.</p>
Full article ">Figure 10
<p>Temperature profiles of (<b>a</b>) rapeseed oil; (<b>b</b>) EVOO; (<b>c</b>) sesame oil; (<b>d</b>) sunflower oil.</p>
Full article ">Figure 11
<p>Graphical dependences of the variation in the maximum temperatures for each sample depending on the time.</p>
Full article ">Figure 12
<p>Change in the temperature profiles of the studied oils over time: (<b>a</b>) at 20 s from the measurement; (<b>b</b>) at 80 s from the measurement; (<b>c</b>) at 120 s from the measurement; (<b>d</b>) and at 160 s from the measurement.</p>
Full article ">Figure 13
<p>(<b>a</b>) Temperature profiles of the studied oils at 20 s from the measurement; (<b>b</b>) first derivative of temperature profiles of the studied oils at 20 s from the measurement.</p>
Full article ">
15 pages, 1691 KiB  
Article
Study on the Characteristics of Crystal Formation and Transformation of Alkali-Activated Slag Minerals Induced by Weak Alkali
by Guodong Huang, Yonghao Huang, Xiaojun Zheng, Fengan Zhang, Jiahao Xu, Jun Qi and Zijian Chen
Crystals 2024, 14(12), 1086; https://doi.org/10.3390/cryst14121086 - 17 Dec 2024
Abstract
Strong-alkali activation is a prerequisite needed to ensure the full polymerization activity of alkali slag binder and establish excellent mechanical properties; however, it substantially increases the preparation cost. In this study, the effects of both strong and weak alkaline activators on the activation [...] Read more.
Strong-alkali activation is a prerequisite needed to ensure the full polymerization activity of alkali slag binder and establish excellent mechanical properties; however, it substantially increases the preparation cost. In this study, the effects of both strong and weak alkaline activators on the activation performance of alkali slag were examined, using a combination of X-ray diffraction, scanning electron microscopy, and Fourier-transform infrared spectroscopy analysis methods. The reaction mechanism was analyzed under different alkaline conditions, and the preparation cost could be significantly reduced without significantly degrading mechanical properties. The results indicate that Ca(OH)2 can stimulate the reactivity of slag, resulting in a 40% decrease in compressive strength (compared to NaOH) but a 25–50% reduction in preparation cost. With increasing Ca(OH)2 dosage, the compressive strength first increases and then decreases. The best excitation effect is achieved at a dosage of 40 g Ca(OH)2 per 450 g GBFS. The formation of aluminosilicate is the main driving force for the observed increase in compressive strength. Excessive dosage of Ca(OH)2 will lead to its deposition in the specimen, thus affecting the development of compressive strength. Full article
(This article belongs to the Section Mineralogical Crystallography and Biomineralization)
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Figure 1
<p>Analysis of NaOH-, Ca(OH)<sub>2</sub>-, and Na<sub>2</sub>CO<sub>3</sub>-induced compressive strength.</p>
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<p>XRD analysis.</p>
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<p>SEM analysis. (<b>a</b>) Specimen N0; (<b>b</b>) specimen N20; (<b>c</b>) specimen N40; (<b>d</b>) specimen C20; (<b>e</b>) specimen C40; (<b>f</b>) specimen C60.</p>
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<p>FT-IR analysis. (<b>a</b>) NaOH excitation; (<b>b</b>) Ca(OH)<sub>2</sub> excitation.</p>
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24 pages, 4996 KiB  
Article
Research and Performance Evaluation of Environmentally Friendly Shale Inhibitor TIL-NH2 for Shale Gas Horizontal Wells
by Yuexin Tian, Xiangjun Liu, Yintao Liu, Haifeng Dong, Guodong Zhang, Biao Su, Xiaofeng Liu, Yifan Hu, Jinjun Huang and Zeze Lu
Molecules 2024, 29(24), 5950; https://doi.org/10.3390/molecules29245950 - 17 Dec 2024
Abstract
Wellbore instability caused by hydration during the development of shale gas reservoirs poses significant challenges to drilling engineering. In this study, a novel and environmentally friendly shale inhibitor, TIL-NH2, was synthesized via free radical polymerization using 1-vinylimidazole and N-(2-bromoethyl)-1,3-propanediamine dihydrobromide as [...] Read more.
Wellbore instability caused by hydration during the development of shale gas reservoirs poses significant challenges to drilling engineering. In this study, a novel and environmentally friendly shale inhibitor, TIL-NH2, was synthesized via free radical polymerization using 1-vinylimidazole and N-(2-bromoethyl)-1,3-propanediamine dihydrobromide as the main raw materials. The molecular structure of TIL-NH2 was characterized by infrared spectroscopy and nuclear magnetic resonance. Incorporating imidazole cations and amino bifunctional groups, TIL-NH2 exhibits excellent inhibitory performance and environmental friendliness. Its performance was systematically evaluated through linear swelling tests, shale cuttings rolling recovery tests, permeability recovery experiments, and dynamic adsorption analyses. The results indicate the following: (1) At a concentration of 1.2 wt%, TIL-NH2 reduced the linear swelling height of shale by 65.69%, significantly outperforming traditional inhibitors like KCl and NW-1. (2) Under conditions of 140 °C, the cuttings rolling recovery rate of TIL-NH2 reached 88.12%, demonstrating excellent high-temperature resistance. (3) Permeability recovery experiments showed that at a concentration of 2.0 wt%, TIL-NH2 achieved a permeability recovery rate of 90.58%, effectively mitigating formation damage. (4) Dynamic adsorption experiments indicated that at a concentration of 2.5 wt%, the adsorption capacity tended toward saturation, reaching 26.00 mg/g, demonstrating stable adsorption capability. Additionally, environmental friendliness evaluations revealed that TIL-NH2 has a degradation rate exceeding 90% within 28 days, and its acute toxicity is significantly lower than that of traditional inhibitors like KCl (the LC50 of TIL-NH2 is 1080.3 mg/L, whereas KCl is only 385.4 mg/L). This research provides a high-efficiency and environmentally friendly new inhibitor for green drilling fluid systems in horizontal shale gas wells, offering important references for technological advancements in unconventional energy development. Full article
(This article belongs to the Topic Petroleum and Gas Engineering, 2nd edition)
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<p>Reaction mechanism equation.</p>
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<p>TIL-NH<sub>2</sub> inhibitor infrared spectra [<a href="#B39-molecules-29-05950" class="html-bibr">39</a>].</p>
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<p><sup>1</sup>H-NMR spectrum of TIL-NH<sub>2</sub> [<a href="#B39-molecules-29-05950" class="html-bibr">39</a>].</p>
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<p>Relationship between shale swelling height and immersion time in TIL-NH<sub>2</sub> solutions with different concentrations.</p>
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<p>Relationship between shale swelling height and immersion time under different concentrations of inhibitor solution.</p>
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<p>Variation in heat rolling recovery with TIL-NH<sub>2</sub> addition at different temperatures.</p>
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<p>Heat roll recovery for each inhibitor at 140 °C.</p>
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<p>Expansion stress of illite in response to different solution treatments.</p>
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<p>Influence of TIL-NH<sub>2</sub> concentration on the swelling stress of illite.</p>
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<p>Effect of combined KCl/TIL-NH<sub>2</sub> solutions on illite swelling stress.</p>
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<p>Triaxial stress diagrams of downhole shale of the Longmaxi Formation soaked by different treatments ((<b>a</b>) water, (<b>b</b>) diesel fuel, (<b>c</b>) white oil, (<b>d</b>) 2% DEM, (<b>e</b>) 2% polyetheramine, (<b>f</b>) TIL-NH<sub>2</sub> solution).</p>
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<p>Variation in shale permeability recovery rates at different TIL-NH<sub>2</sub> concentrations.</p>
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<p>Dynamic adsorption as a function of TIL-NH<sub>2</sub> concentration.</p>
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<p>Influence of KCl concentration on the anti-swelling effectiveness of TIL-NH<sub>2</sub>.</p>
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<p>Biodegradation rates of different concentrations of TIL-NH<sub>2</sub> as a function of time.</p>
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<p>Flowchart summarizing the experimental design and workflow of this study.</p>
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16 pages, 1285 KiB  
Article
Different Correlation Patterns Between Circulating Amino Acids and Body Temperature in Fibromyalgia Syndrome: A Cross-Sectional Study
by Antonio Casas-Barragán, Francisco Molina, Rosa María Tapia-Haro, José Manuel Martínez-Martos, María Jesús Ramírez-Expósito, Alma Rus, María Correa-Rodríguez and María Encarnación Aguilar-Ferrándiz
Int. J. Mol. Sci. 2024, 25(24), 13517; https://doi.org/10.3390/ijms252413517 - 17 Dec 2024
Abstract
The aim of this study was to analyze the association between circulating amino acids and central and peripheral body temperature in subjects with and without fibromyalgia syndrome (FMS). A total of 47 patients with FMS and 59 healthy subjects were included in the [...] Read more.
The aim of this study was to analyze the association between circulating amino acids and central and peripheral body temperature in subjects with and without fibromyalgia syndrome (FMS). A total of 47 patients with FMS and 59 healthy subjects were included in the study. The concentration of amino acids was determined in serum samples using a fluorimeter coupled with a high-performance liquid chromatography system. An infrared thermography camera was used to estimate peripheral hand temperatures. The core temperature of the body was estimated using an infrared thermometer, which was applied to the axillary and tympanic areas. Correlations between several thermographic variables of the hands and tryptophan, methionine, 3-methylhistidine, histidine, glutamic acid, and tyrosine were identified exclusively within the FMS group. In contrast, correlations between aminoadipic acid and serine and thermographic variables were observed only in the healthy control group. The concentrations of asparagine and lysine correlated with thermographic variables in both groups. The essential amino acid leucine was found to correlate with axillary temperature in FMS patients. However, it should be noted that the observed associations between aminoadipic acid and tryptophan blood concentrations and axillary temperature were limited to the control group. Several correlations were identified between circulating amino acids and different body temperatures in both healthy controls and patients with FMS. However, the correlation pattern differs significantly between FMS patients and healthy controls. These findings suggest the possibility of a change in the function of several amino acids in the thermoregulatory process in patients with FMS. Full article
(This article belongs to the Special Issue Amino Acids and Related Compounds in Health and Disease)
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<p>Flow diagram of the patient screening process for study enrollment.</p>
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<p>Linear regression standardized P-P plot of predictive factors associated with peripheral and central temperature in both populations.</p>
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<p>Thermograms of the hands in a patient with fibromyalgia and in a healthy woman. (<b>A</b>) Thermographic image of the dorsal area of both hands of a woman diagnosed with fibromyalgia (El1 and El7 = thumb finger; El2 and El8 = index finger; El3 and El9 = middle finger; El4 and El10 = ring finger; El5 and El11 = pinkie finger; El6 and El12 = dorsal centre). (<b>B</b>) Thermographic image of the palmar area of both hands of a healthy woman (El1 and El9 = thumb finger; El2 and El10 = index finger; El3 and El11 = middle finger; El4 and El12 = ring finger; El5 and El13 = pinkie finger; El6 and El14 = thenar eminence; El7 and El15 = palmar centre; El8 and El16 = hipothenar eminence). Red triangles = the point of maximum temperature within each area. Blue triangles = the point of minimum temperature within each area.</p>
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12 pages, 1852 KiB  
Article
Nondestructive Determination of Tocopherol and Tocotrienol in Vitamin E Powder Using Near- and Mid-Infrared Spectroscopy
by Saowaluk Rungchang, Sila Kittiwachana, Sujitra Funsueb, Chitsiri Rachtanapun, Juthamas Tantala, Phumon Sookwong, Laichheang Yort, Chayanid Sringarm and Sudarat Jiamyangyuen
Foods 2024, 13(24), 4079; https://doi.org/10.3390/foods13244079 - 17 Dec 2024
Abstract
Vitamin E is an essential nutrient, but its poor water solubility limits food and pharmaceutical applications. The usability of vitamin E can be enhanced via modification methods such as encapsulation, which transforms the physical state of vitamin E from a liquid to a [...] Read more.
Vitamin E is an essential nutrient, but its poor water solubility limits food and pharmaceutical applications. The usability of vitamin E can be enhanced via modification methods such as encapsulation, which transforms the physical state of vitamin E from a liquid to a powder. This study examined the efficacy of near-infrared (NIR) and mid-infrared (MIR) spectroscopy in identifying and predicting various vitamin E derivatives in vitamin E-encapsulated powder (VEP). An MIR analysis revealed the fundamental C–H vibrations of vitamin E in the range of 2700–3250 cm−1, whereas an NIR analysis provided information about the corresponding combination, first, and second overtones in the range of 4000–9000 cm−1. The MIR and NIR data were analyzed using a principal component analysis to characterize the VEP. Partial least squares (PLS) regression was applied to predict the content of individual vitamin E derivatives. PLS cross-validation revealed that NIR analysis provides more reliable predictive accuracy and precision for the contents of vitamin E derivatives, achieving a higher coefficient of determination for prediction (Q2) (0.92–0.99) than MIR analysis (0.20–0.85). For test set validation, the NIR predictions exhibited a significant level of accuracy, as indicated by a high ratio of prediction to deviation (RPD) and Q2. Furthermore, the PLS models developed using the NIR data had statistically significant predictive performance, with a high RPD (1.54–3.92) and Q2 (0.66–0.94). Thus, NIR spectroscopy is a valuable nondestructive technique for analyzing vitamin E samples, while MIR spectroscopy serves as a useful method for confirming its presence. Full article
(This article belongs to the Section Food Analytical Methods)
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<p>(<b>a</b>) NIR and (<b>b</b>) MIR spectra of encapsulated vitamin E.</p>
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<p>PCA score and loading plots of (<b>a</b>) NIR and (<b>b</b>) MIR data for encapsulated vitamin E.</p>
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<p>Scatter plots of the actual and predicted quality parameters for the NIR spectra of encapsulated vitamin E.</p>
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<p>PLS coefficients for the NIR spectra of encapsulated vitamin E.</p>
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19 pages, 4141 KiB  
Article
Study on the Curing Behaviors of Benzoxazine Nitrile-Based Resin Featuring Fluorene Structures and the Excellent Properties of Their Glass Fiber-Reinforced Laminates
by Mingzhen Xu, Lunshuai He, Jiaqu Zhang, Zexu Fan and Bo Li
Materials 2024, 17(24), 6167; https://doi.org/10.3390/ma17246167 - 17 Dec 2024
Abstract
Benzoxazine and o-phthalonitrile resin are two of the most eminent polymer matrices within high-performance fiber-reinforced resin-based composite materials. Studying the influence modalities of their structures and forming processes on performance can furnish a theoretical basis for the design and manufacturing of superior performance [...] Read more.
Benzoxazine and o-phthalonitrile resin are two of the most eminent polymer matrices within high-performance fiber-reinforced resin-based composite materials. Studying the influence modalities of their structures and forming processes on performance can furnish a theoretical basis for the design and manufacturing of superior performance composite materials. In this study, we initially incorporated a fluorene structure into the molecular main chain through molecular design to prepare a fluorene-containing benzoxazine nitrile-based resin. The polymerization reaction behavior and process of this resin were monitored meticulously using differential scanning calorimetry and infrared spectroscopy. Meanwhile, by manipulating the pre-polymerization reaction conditions, the impact of the pre-polymerization reaction on the polymerization behavior of the resin monomer was investigated, respectively. Subsequently, diverse glass fiber-reinforced resin-based composite materials were fabricated via hot-pressing in combination with a programmed temperature rise process. Through the characterization of structural strength and thermomechanical properties, it was found that the composite laminates all manifested outstanding bending strength (~600 MPa) and modulus (>30 GPa). Nevertheless, with the elevation of the post-curing temperature, the structural strength and modulus of the composite materials displayed distinct variation laws. This study also discussed the variation laws of the thermal properties of the composite materials by analyzing the glass transition temperature and crosslinking density. Additionally, the interface bonding effect between the glass fiber and the resin matrix was deliberated through the analysis of the cross-sectional morphology of the composite laminates. The results demonstrated that this work proposes an improved matrix resin system with outstanding thermal stability and mechanical properties that broadens the foundation and ideas for subsequent research. Full article
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<p>The synthesis process of the WZ-cn monomer.</p>
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<p>(<b>a</b>) DSC curves and (<b>b</b>) FTIR spectrum of various WZ-cn pre-polymers.</p>
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<p>The chromatograms of various WZ-cn pre-polymers: (<b>a</b>) WZ-cn-30, (<b>b</b>) WZ-cn-60, and (<b>c</b>) WZ-cn-90.</p>
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<p>DSC time sweep of the WZ-cn-90 pre-polymer.</p>
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<p>FTIR spectrum of the WZ-cn-90 pre-polymer cured at various temperatures.</p>
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<p>(<b>a</b>,<b>b</b>) The free hydrogen catalyzes the ring-opening polymerization of the oxazine ring in WZ-cn to form the Mannich bridge structure; (<b>c</b>) the active group in the Mannich bridge catalyzes the ring-forming polymerization of the nitrile group in WZ-cn to form a triazine ring and a phthalocyanine ring; and (<b>d</b>) possible structure of the WZ-cn polymer.</p>
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<p>The TGA analysis curves of WZ-cn/GF composite laminates treated at various temperatures: (<b>a</b>) TGA; (<b>b</b>) zoom into view.</p>
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<p>Schematic diagram of S1, S2, and S3 in the formulas A* and K*.</p>
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<p>The DMA analysis curves of WZ-cn/GF composite laminates treated at various temperatures: (<b>a</b>) storage modulus; (<b>b</b>) Tan δ.</p>
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<p>(<b>a</b>) Flexural strength and (<b>b</b>) flexural modulus of various WZ-cn/GF composite laminates.</p>
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<p>SEM images of the fracture surface of various WZ-cn/GF composite laminates: (<b>a</b>) and (<b>a-1</b>) WZ-cn/GF-200; (<b>b</b>) and (<b>b-1</b>) WZ-cn/GF-240; and (<b>c</b>) and (<b>c-1</b>) WZ-cn/GF-280.</p>
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16 pages, 4329 KiB  
Article
Porphyrin-Based Aluminum Metal-Organic Framework with Copper: Pre-Adsorption of Water Vapor, Dynamic and Static Sorption of Diethyl Sulfide Vapor, and Sorbent Regeneration
by Mohammad Shahwaz Ahmad and Alexander Samokhvalov
Materials 2024, 17(24), 6160; https://doi.org/10.3390/ma17246160 - 17 Dec 2024
Viewed by 70
Abstract
Metal–organic frameworks (MOFs) are hybrid inorganic–organic 3D coordination polymers with metal sites and organic linkers, which are a “hot” topic in the research of sorption, separations, catalysis, sensing, and environmental remediation. In this study, we explore the molecular mechanism and kinetics of interaction [...] Read more.
Metal–organic frameworks (MOFs) are hybrid inorganic–organic 3D coordination polymers with metal sites and organic linkers, which are a “hot” topic in the research of sorption, separations, catalysis, sensing, and environmental remediation. In this study, we explore the molecular mechanism and kinetics of interaction of the new copper porphyrin aluminum metal–organic framework (actAl-MOF-TCPPCu) compound 4 with a vapor of the volatile organic sulfur compound (VOSC) diethyl sulfide (DES). First, compound 4 was synthesized by post-synthetic modification (PSM) of Al-MOF-TCPPH2 compound 2 by inserting Cu2+ ions into the porphyrin ring and characterized by complementary qualitative and quantitative chemical, structural, and spectroscopic analysis. Second, the interaction of compound 4 with DES vapor was analyzed dynamically by the novel method of in situ time-dependent attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy at controlled humidity levels. The sorbent–adsorbate interactions, as analyzed by the shifts in IR peaks, indicate that the bonding includes the hydroxy O-H, carboxylate COO, and phenyl groups. The kinetics of sorption obeys the Langmuir pseudo-first-order rate law. The pre-adsorption of water vapor by compound 4 at the controlled relative humidity under static (equilibrium) conditions yields the binary stoichiometric adsorption complex (Al-MOF-TCPPCu)1.0(H2O)8.0. The pre-adsorption of water vapor makes the subsequent sorption of DES slower, while the kinetics obey the same rate law. Then, static pre-adsorption of water vapor was followed by static sorption of DES vapor, and the ternary adsorption complex (Al-MOF-TCPPCu)1.0(H2O)8.0(DES)3.8 was obtained. Despite the pre-adsorption of significant amounts of water, the binary complex adsorbs a large amount of DES: ca. 36.6 wt. % (per compound 4). Finally, the ternary complex is facilely regenerated by gentle heating under vacuum. Compound 4 and related MOFs are promising for adsorptive removal of vapor of DES and related VOSCs from dry and humid air. Full article
(This article belongs to the Special Issue Adsorbents and Their Applications (Second Volume))
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<p>Diethyl sulfide and its presence in nature, technology, and the environment.</p>
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<p>The 2D molecular structure of the structural unit of copper-containing porphyrin aluminum MOF, compound <b>4</b> actAl-MOF-TCPPCu.</p>
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<p>Powder XRD patterns of activated compounds: (<b>a</b>) compound <b>2</b> actAl-MOF-TCPPH<sub>2</sub>; (<b>b</b>) the target compound <b>4</b> actAl-MOF-TCPPCu.</p>
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<p>The starting in situ time-dependent ATR-FTIR spectra of compound 4 in the flow of DES vapor. (<b>a</b>) High wavenumbers; (<b>b</b>) mid-IR; (<b>c</b>) low wavenumbers.</p>
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<p>The proposed model of bonding DES molecules to compound <b>4</b>.</p>
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<p>Kinetics of in situ sorption of DES vapor by the activated compound <b>4</b>. (<b>a</b>) Integration of IR peak due to the asymmetric CH<sub>2</sub> stretching at 2965 cm<sup>−1</sup>; (<b>b</b>) kinetic analysis of the integrated peak.</p>
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<p>The in situ time-dependent ATR-FTIR spectra of the binary adsorption complex hydAl-MOF-TCPPCu in the flow of DES vapor. (<b>a</b>) High wavenumber range; (<b>b</b>) mid-IR range; (<b>c</b>) low wavenumber range.</p>
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<p>Kinetics of in situ sorption of DES vapor by compound <b>4hyd</b>. (<b>a</b>) Integrated IR peak of asymmetric CH<sub>2</sub> stretching; (<b>b</b>) formal kinetic analysis of peak area in time.</p>
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<p>Powder XRD patterns of sorbent compound 4 and its adsorption complexes. (<b>a</b>) actAl-MOF-TCPPCu and hydAl-MOF-TCPPCu (binary adsorption complex). (<b>b</b>) hydAl-MOF-TCPPCu and DES-hydAl-MOF-TCPPCu (ternary adsorption complex). (<b>c</b>) actAl-MOF-TCPPCu and regAl-MOF-TCPPCu (regenerated ternary adsorption complex).</p>
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11 pages, 2922 KiB  
Article
The Trace-Element Characteristics of Chrysoberyl: Insights from Compositional and Spectroscopic Analyses
by Linling Dong, Yimiao Liu, Xinxin Gao and Ren Lu
Minerals 2024, 14(12), 1280; https://doi.org/10.3390/min14121280 - 17 Dec 2024
Viewed by 119
Abstract
To characterize the trace-element characteristics of chrysoberyl, we studied twenty-six chrysoberyl samples from various localities by using laser ablation inductively coupled plasma mass spectrometry (LA–ICP–MS), photoluminescence (PL), and ultraviolet–visible–near-infrared (UV–Vis–NIR) spectroscopy. Chemical analysis has confirmed the existence of trace elements, including Fe, Ti, [...] Read more.
To characterize the trace-element characteristics of chrysoberyl, we studied twenty-six chrysoberyl samples from various localities by using laser ablation inductively coupled plasma mass spectrometry (LA–ICP–MS), photoluminescence (PL), and ultraviolet–visible–near-infrared (UV–Vis–NIR) spectroscopy. Chemical analysis has confirmed the existence of trace elements, including Fe, Ti, Ga, Sn, B, Cr, and V. The phenomenon of ionic isomorphic substitution frequently occurs at lattice sites within chrysoberyl. Notably, the isomorphic substitution of Al3+ in octahedral sites is significant, with the primary substituting elements being Fe, Ti, Cr, V, Ga, and Sn. The PL spectra of chrysoberyl samples exhibit sharp peaks at 678 and 680 nm, which are attributed to Cr3+, even in samples in which the Cr concentration is below the detection limit of LA-ICP-MS. This demonstrates the high-sensitivity feature of PL spectroscopy. The UV–Vis–NIR spectra of chrysoberyl samples consistently exhibit a band at 440 nm, and strong double narrow bands near 367 nm and 375 nm are observed. These spectral features are associated with Fe3+ chromophores—specifically, Fe3+-Fe3+ pairs or clusters and Fe3+ ions, respectively. By combining LA–ICP–MS analysis and PL mapping on a sample exhibiting color zoning, it has been found that the darker sections contain a higher concentration of Cr compared to the lighter sections, while the concentrations of other elements remain largely consistent. In other words, subtle variations in Cr concentration may be the underlying cause of color zoning in chrysoberyl. Full article
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<p>Rough and polished chrysoberyl samples from various localities: (<b>A</b>) Myanmar; (<b>B</b>) Sri Lanka; (<b>C</b>) Tanzania; (<b>D</b>) India; (<b>E</b>) Brazil.</p>
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<p>The photoluminescence spectra of chrysoberyl samples. The spectral directions are in the same orientation. (<b>A</b>) Increasing Cr concentration; (<b>B</b>) Cr concentrations below the detection limit of LA-ICP-MS.</p>
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<p>The UV–Vis–NIR spectra of chrysoberyl samples. The spectral directions are in the same orientation.</p>
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<p>The elemental ternary plots illustrate the relationships between chemical composition and origins. (<b>A</b>) The Fe-Ti-Sn diagram; (<b>B</b>) The Fe-Ti-Ga diagram; (<b>C</b>) The Fe-Ga-Sn diagram; (<b>D</b>) The B-V-Cr diagram.</p>
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<p>An approximate linear negative correlation between the content of Al and the content of octahedral-site substituting metal ions (Me<sup>n+</sup>). The dashed line represents the linear fit for the content of Al and Me<sup>n+</sup>.</p>
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<p>The relationship between trace elements and Me<sup>n+</sup> concentration in chrysoberyl samples. (<b>A</b>) The relationship between Me<sup>n+</sup> and Fe. The dashed line represents the linear fit for the content of Fe and Me<sup>n+</sup>; (<b>B</b>) the relationship between Me<sup>n+</sup> and Ti. The dashed line is the approximation of the content of Ti and Me<sup>n+</sup>.</p>
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<p>The UV–Vis–NIR spectra of chrysoberyl sample S3. CIE L*a*b* coordinates of color circles here are calculated under D65 light for a 1 cm wafer thickness to demonstrate color features of chrysoberyl at the different sections of the zoning.</p>
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<p>Laser PL mapping of chrysoberyl sample S3: (<b>A</b>) at 678 nm; (<b>B</b>) at 680 nm; (<b>C</b>) schematic diagram of the test area.</p>
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33 pages, 5819 KiB  
Article
Blind Infrared Remote-Sensing Image Deblurring Algorithm via Edge Composite-Gradient Feature Prior and Detail Maintenance
by Xiaohang Zhao, Mingxuan Li, Ting Nie, Chengshan Han and Liang Huang
Remote Sens. 2024, 16(24), 4697; https://doi.org/10.3390/rs16244697 - 16 Dec 2024
Viewed by 186
Abstract
The problem of blind image deblurring remains a challenging inverse problem, due to the ill-posed nature of estimating unknown blur kernels and latent images within the Maximum A Posteriori (MAP) framework. To address this challenge, traditional methods often rely on sparse regularization priors [...] Read more.
The problem of blind image deblurring remains a challenging inverse problem, due to the ill-posed nature of estimating unknown blur kernels and latent images within the Maximum A Posteriori (MAP) framework. To address this challenge, traditional methods often rely on sparse regularization priors to mitigate the uncertainty inherent in the problem. In this paper, we propose a novel blind deblurring model based on the MAP framework that leverages Composite-Gradient Feature (CGF) variations in edge regions after image blurring. This prior term is specifically designed to exploit the high sparsity of sharp edge regions in clear images, thereby effectively alleviating the ill-posedness of the problem. Unlike existing methods that focus on local gradient information, our approach focuses on the aggregation of edge regions, enabling better detection of both sharp and smoothed edges in blurred images. In the blur kernel estimation process, we enhance the accuracy of the kernel by assigning effective edge information from the blurred image to the smoothed intermediate latent image, preserving critical structural details lost during the blurring process. To further improve the edge-preserving restoration, we introduce an adaptive regularizer that outperforms traditional total variation regularization by better maintaining edge integrity in both clear and blurred images. The proposed variational model is efficiently implemented using alternating iterative techniques. Extensive numerical experiments and comparisons with state-of-the-art methods demonstrate the superior performance of our approach, highlighting its effectiveness and real-world applicability in diverse image-restoration tasks. Full article
21 pages, 4834 KiB  
Article
Thermal, Molecular Dynamics, and Mechanical Properties of Poly(Ethylene Furanoate)/Poly(ε-Caprolactone) Block Copolymers
by Johan Stanley, Panagiotis A. Klonos, Aikaterini Teknetzi, Nikolaos Rekounas, Apostolos Kyritsis, Lidija Fras Zemljič, Dimitra A. Lambropoulou and Dimitrios N. Bikiaris
Molecules 2024, 29(24), 5943; https://doi.org/10.3390/molecules29245943 - 16 Dec 2024
Viewed by 380
Abstract
This study presents the synthesis and characterization of a series of multiblock copolymers, poly(ethylene 2,5-furandicarboxylate)-poly(ε-caprolactone) (PEF-PCL), created through a combination of the two-step melt polycondensation method and ring opening polymerization, as sustainable alternatives to fossil-based plastics. The structural confirmation of these block copolymers [...] Read more.
This study presents the synthesis and characterization of a series of multiblock copolymers, poly(ethylene 2,5-furandicarboxylate)-poly(ε-caprolactone) (PEF-PCL), created through a combination of the two-step melt polycondensation method and ring opening polymerization, as sustainable alternatives to fossil-based plastics. The structural confirmation of these block copolymers was achieved through Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy (ATR-FTIR), ensuring the successful integration of PEF and PCL segments. X-ray Photoelectron Spectroscopy (XPS) was employed for chemical bonding and quantitative analysis, providing insights into the distribution and compatibility of the copolymer components. Differential Scanning Calorimetry (DSC) analysis revealed a single glass transition temperature (Tg), indicating the effective plasticizing effect of PCL on PEF, which enhances the flexibility of the copolymers. X-ray Diffraction (XRD) studies highlight the complex relationship between PCL content and crystallization in PEF-PCL block copolymers, emphasizing the need to balance crystallinity and mechanical properties for optimal material performance. Broadband Dielectric Spectroscopy (BDS) confirmed excellent distribution of PEF-PCL without phase separation, which is vital for maintaining consistent material properties. Mechanical properties were evaluated using Nanoindentation testing, demonstrating the potential of these copolymers as flexible packaging materials due to their enhanced mechanical strength and flexibility. The study concludes that PEF-PCL block copolymers are promising candidates for sustainable packaging solutions, combining environmental benefits with desirable material properties. Full article
(This article belongs to the Special Issue Macromolecular Chemistry in Europe)
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<p>ATR-FTIR spectra of neat PEF, neat PCL, and block copolymers.</p>
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<p>XPS survey of sample neat PEF, PCL, and their copolymers.</p>
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<p>High-resolution XPS spectrum of core level C 1s for neat PEF and PCL samples and their copolymers.</p>
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<p>Comparative DSC traces for all samples and both scans performed. (<b>a</b>) during quenching, (<b>b</b>) subsequent heating after quenching, (<b>c</b>) cooling with 80–100 K/min and (<b>d</b>) subsequent heating after (<b>c</b>). The recorded heat flow is presented upon normalization to the mass of each sample, while the added arrows mark the recorded effects of PCL addition on the glass transition.</p>
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<p>Effects on (<b>a</b>) the glass transition temperature, <span class="html-italic">T<sub>g</sub></span>, and (<b>b</b>) the corresponding heat capacity change, Δ<span class="html-italic">c<sub>p</sub></span>.</p>
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<p>XRD patterns of amorphous neat PEF, neat PCL, and block copolymers.</p>
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<p>Comparative isochronal <span class="html-italic">ε</span>″(<span class="html-italic">T</span>) plots for all samples, showing the plasticization action of PCL over PEF (acceleration of the segmental relaxation, <span class="html-italic">α</span>).</p>
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<p>(<b>a</b>) Segmental dynamics map for all samples. (<b>b</b>) The PCL fraction effect on the dielectric/calorimetric <span class="html-italic">T</span><sub>g</sub> and on the fragility of <span class="html-italic">α</span> relaxation.</p>
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<p>(<b>a</b>) Isothermal curves of the AC conductivity, <span class="html-italic">σ</span>’(<span class="html-italic">f, T</span>), for neat PEF and P1090, showing that the formation of DC plateau due to ionic conductivity occurs uniquely at <span class="html-italic">T</span> &gt; <span class="html-italic">T</span><sub>g</sub>. (<b>b</b>) Comparative curves of <span class="html-italic">σ</span>’ at the lowest frequency of recording against the reciprocal temperature (Arrhenius plots of conductivity) for all samples.</p>
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<p>(<b>a</b>) Hardness and (<b>b</b>) reduced modulus values of block copolymers with standard deviation.</p>
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<p>The decrease in (<b>a</b>) hardness and (<b>b</b>) reduced modulus values with respect to ε-CL content.</p>
Full article ">Scheme 1
<p>Synthesis route to PEF and PEF-PCL block copolymers.</p>
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20 pages, 1467 KiB  
Article
Clustering-Based Thermography for Detecting Multiple Substances Under Large-Scale Floating Covers
by Yue Ma, Benjamin Steven Vien, Thomas Kuen and Wing Kong Chiu
Sensors 2024, 24(24), 8030; https://doi.org/10.3390/s24248030 - 16 Dec 2024
Viewed by 190
Abstract
This study presents a novel approach for monitoring waste substrate digestion under high-density polyethylene (HDPE) geomembranes in sewage treatment plants. The method integrates infrared thermal imaging with a clustering algorithm to predict the distribution of various substrates beneath Traditional outdoor large-scale opaque geomembranes, [...] Read more.
This study presents a novel approach for monitoring waste substrate digestion under high-density polyethylene (HDPE) geomembranes in sewage treatment plants. The method integrates infrared thermal imaging with a clustering algorithm to predict the distribution of various substrates beneath Traditional outdoor large-scale opaque geomembranes, using solar radiation as an excitation source. The technique leverages ambient weather conditions to assess the thermal responses of HDPE covers. Cooling constants are used to reconstruct thermal images, and clustering algorithms are explored to segment and identify different material states beneath the covers. Laboratory experiments have validated the algorithm’s effectiveness in accurately classifying varied regions by analyzing transient temperature variations caused by natural excitations. This method provides critical insights into scum characteristics and biogas collection processes, thereby enhancing decision-making in sewage treatment management. The methodology under development is anticipated to undergo rigorous evaluation across various floating covers at a large-scale sewage treatment facility in Melbourne. Subsequent to field validation, the implementation of an on-site, continuous thermography monitoring system is envisioned to be further advanced. Full article
19 pages, 35488 KiB  
Article
Downscaling Land Surface Temperature via Assimilation of LandSat 8/9 OLI and TIRS Data and Hypersharpening
by Luciano Alparone and Andrea Garzelli
Remote Sens. 2024, 16(24), 4694; https://doi.org/10.3390/rs16244694 - 16 Dec 2024
Viewed by 196
Abstract
Land surface temperature (LST) plays a pivotal role in many environmental sectors. Unfortunately, thermal bands produced by instruments that are onboard satellites have limited spatial resolutions; this seriously impairs their potential usefulness. In this study, we propose an automatic procedure for the spatial [...] Read more.
Land surface temperature (LST) plays a pivotal role in many environmental sectors. Unfortunately, thermal bands produced by instruments that are onboard satellites have limited spatial resolutions; this seriously impairs their potential usefulness. In this study, we propose an automatic procedure for the spatial downscaling of the two 100 m thermal infrared (TIR) bands of LandSat 8/9, captured by the TIR spectrometer (TIRS), by exploiting the bands of the optical instrument. The problem of fusion of heterogeneous data is approached as hypersharpening: each of the two sharpening images is synthesized following data assimilation concepts, with the linear combination of 30 m optical bands and the 15 m panchromatic (Pan) image that maximizes the correlation with each thermal channel at its native 100 m scale. The TIR bands resampled at 15 m are sharpened, each by its own synthetic Pan. On two different scenes of an OLI-TIRS image, the proposed approach is compared with 100 m to 15 m pansharpening, carried out uniquely by means of the Pan image of OLI and with the two high-resolution assimilated thermal images that are used for hypersharpening the two TIRS bands. Besides visual evaluations of the temperature maps, statistical indexes measuring radiometric and spatial consistencies are provided and discussed. The superiority of the proposed approach is highlighted: the classical pansharpening approach is radiometrically accurate but weak in the consistency of spatial enhancement. Conversely, the assimilated TIR bands, though adequately sharp, lose more than 20% of radiometric consistency. Our proposal trades off the benefits of its counterparts in a unique method. Full article
(This article belongs to the Special Issue Remote Sensing for Land Surface Temperature and Related Applications)
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