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19 pages, 11406 KiB  
Article
Mechanical, Tribological, and Corrosion Resistance Properties of (TiAlCrNbY)Ny High-Entropy Coatings Synthesized Through Hybrid Reactive Magnetron Sputtering
by Nicolae C. Zoita, Mihaela Dinu, Anca C. Parau, Iulian Pana and Adrian E. Kiss
Crystals 2024, 14(11), 993; https://doi.org/10.3390/cryst14110993 (registering DOI) - 17 Nov 2024
Abstract
This study investigates the effects of aluminum and nitrogen content on the microstructure, mechanical properties, and tribological performance of high-entropy coatings based on (TiCrAlNbY)Ny systems. Using a hybrid magnetron sputtering technique, both metallic and nitride coatings were synthesized and evaluated. [...] Read more.
This study investigates the effects of aluminum and nitrogen content on the microstructure, mechanical properties, and tribological performance of high-entropy coatings based on (TiCrAlNbY)Ny systems. Using a hybrid magnetron sputtering technique, both metallic and nitride coatings were synthesized and evaluated. Increasing the aluminum concentration led to a transition from a crystalline to a nanocrystalline and nearly amorphous (NC/A) structure, with the TiAl0.5CrNbY sample (11.8% Al) exhibiting the best balance of hardness (6.8 GPa), elastic modulus (87.1 GPa), and coefficient of friction (0.64). The addition of nitrogen further enhanced these properties, transitioning the coatings to a denser fine-grained FCC structure. The HN2 sample (45.8% nitrogen) displayed the highest hardness (21.8 GPa) but increased brittleness, while the HN1 sample (32.9% nitrogen) provided an optimal balance of hardness (14.3 GPa), elastic modulus (127.5 GPa), coefficient of friction (0.60), and wear resistance (21.2 × 10⁻⁶ mm3/Nm). Electrochemical impedance spectroscopy revealed improved corrosion resistance for the HN1 sample due to its dense microstructure. Overall, the (TiAl0.5CrNbY)N0.5 coating achieved the best performance for friction applications, such as break and clutch systems, requiring high coefficients of friction, high wear resistance, and durability. Full article
(This article belongs to the Special Issue Advances of High Entropy Alloys)
17 pages, 3050 KiB  
Article
Nonlinear Vibrations of Low Pressure Turbine Bladed Disks: Tests and Simulations
by Umidjon Usmanov, Giuseppe Battiato, Christian Maria Firrone, Marta Conte, Emanuele Rosso and Antonio Giuseppe D’Ettole
Appl. Sci. 2024, 14(22), 10597; https://doi.org/10.3390/app142210597 (registering DOI) - 17 Nov 2024
Abstract
One of the most effective methods to limit the mechanical vibrations of bladed disks is the use of friction damping at mechanical joint interfaces. Unfortunately, dedicated tests to assess the impact of mistuning and the effectiveness of friction dampers are uncommon. This paper [...] Read more.
One of the most effective methods to limit the mechanical vibrations of bladed disks is the use of friction damping at mechanical joint interfaces. Unfortunately, dedicated tests to assess the impact of mistuning and the effectiveness of friction dampers are uncommon. This paper presents an original design of an academic demonstrator to perform an experimental analysis of the dynamic response of a tip-free bladed disk with under-platform dampers (UPDs) , including an identification of intrinsic and contact mistuning introduced by the UPDs. The 48-blade disk was tested in a vacuum spinning rig by using permanent magnets. Vibration measurements were performed with the Blade Tip-Timing system. Tests were simulated using the Policontact tool, which predicted the average experimental nonlinear response in the presence of UPD, confirming the tool’s ability to capture the general nonlinear dynamic behavior of the mistuned bladed disk. This study presents a novel approach combining experimental Blade Tip Timing (BTT) with numerical simulations using Policontact (ver. 3.0) software and a model update based on experimental evidence to validate nonlinear dynamic responses. It distinguishes between intrinsic and contact mistuning effects, providing new insights into their impact on bladed disk vibrations. Additionally, a comparison of aluminum and steel UPDs reveals that steel offers a 26% greater damping efficiency due to its higher density and preload, significantly improving vibration reduction. Full article
(This article belongs to the Special Issue Advances in Structural Design for Turbomachinery Applications)
12 pages, 5559 KiB  
Article
Potassium-Based Solid Sorbents for CO2 Adsorption: Key Role of Interconnected Pores
by Yuan Zhao, Jiangbo Huo, Xuefei Wang and Shunwei Ma
Nanomaterials 2024, 14(22), 1838; https://doi.org/10.3390/nano14221838 (registering DOI) - 17 Nov 2024
Abstract
Industrial CO2 emissions contribute to pollution and greenhouse effects, highlighting the importance of carbon capture. Potassium carbonate (K2CO3) is an effective CO2 absorbent, yet its liquid-phase absorption faces issues like diffusion resistance and corrosion risks. In this [...] Read more.
Industrial CO2 emissions contribute to pollution and greenhouse effects, highlighting the importance of carbon capture. Potassium carbonate (K2CO3) is an effective CO2 absorbent, yet its liquid-phase absorption faces issues like diffusion resistance and corrosion risks. In this work, the solid adsorbents were developed with K2CO3 immobilized on the selected porous supports. Al2O3 had an optimum CO2 adsorption capacity of 0.82 mmol g−1. After further optimization of its pore structure, the self-prepared support Al2O3-2, which has an average pore diameter of 11.89 nm and a pore volume of 0.59 cm3 g−1, achieved a maximum CO2 adsorption capacity of 1.12 mmol g−1 following K2CO3 impregnation. Additionally, the relationship between support structure and CO2 adsorption efficiency was also analyzed. The connectivity of the pores and the large pore diameter of the support may play a key role in enhancing CO2 adsorption performance. During 10 cycles of testing, the K2CO3-based adsorbents demonstrated consistent high CO2 adsorption capacity with negligible degradation. Full article
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Figure 1

Figure 1
<p>Schematic diagram of the experimental setup for CO<sub>2</sub> adsorption assessment.</p>
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<p>CO<sub>2</sub> adsorption capacities of the 20% K<sub>2</sub>CO<sub>3</sub>/supports under the conditions: 10 vol% CO<sub>2</sub> in air, 298 K adsorption temperature.</p>
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<p>(<b>a</b>–<b>d</b>) CO<sub>2</sub> adsorption capacities of 20% K<sub>2</sub>CO<sub>3</sub>/Al<sub>2</sub>O<sub>3</sub>-2 adsorbents by varying preparation conditions.</p>
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<p>XRD patterns of Al<sub>2</sub>O<sub>3</sub>-1 and Al<sub>2</sub>O<sub>3</sub>-2.</p>
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<p>SEM images of Al<sub>2</sub>O<sub>3</sub>-1 (<b>a</b>,<b>b</b>) and Al<sub>2</sub>O<sub>3</sub>-2 (<b>c</b>,<b>d</b>).</p>
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<p>N<sub>2</sub> adsorption (hollow) and desorption (solid) isotherms of Al<sub>2</sub>O<sub>3</sub>-1 and Al<sub>2</sub>O<sub>3</sub>-2.</p>
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<p>Pore size distributions of Al<sub>2</sub>O<sub>3</sub>-1 and Al<sub>2</sub>O<sub>3</sub>-2.</p>
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<p>A comparative schematic of CO<sub>2</sub> diffusion in interconnected and non-interconnected pore channels. The arrow represents the direction of molecular diffusion.</p>
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<p>TGA curves of Al<sub>2</sub>O<sub>3</sub>-1 and Al<sub>2</sub>O<sub>3</sub>-2.</p>
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<p>Recycling performance of 20% K<sub>2</sub>CO<sub>3</sub>/Al<sub>2</sub>O<sub>3</sub>-2 adsorbent after 10 cycles.</p>
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14 pages, 3441 KiB  
Article
Metal-Exchanged Phosphomolybdic Acid Salts-Catalyzed Esterification of Levulinic Acid
by Márcio José da Silva, Alana Alves Rodrigues and Wilton Keisuke Taba
Processes 2024, 12(11), 2574; https://doi.org/10.3390/pr12112574 (registering DOI) - 17 Nov 2024
Abstract
We examined the effectiveness of metal-exchanged phosphomolybdic acid salts in converting levulinic acid, derived from biomass, into valuable products (alkyl levulinate). We prepared salts of phosphomolybdic acid using different metals (Fe3+, Al3+, Zn2+, Cu2+, Mn [...] Read more.
We examined the effectiveness of metal-exchanged phosphomolybdic acid salts in converting levulinic acid, derived from biomass, into valuable products (alkyl levulinate). We prepared salts of phosphomolybdic acid using different metals (Fe3+, Al3+, Zn2+, Cu2+, Mn2+, Ni2+, and Co2+). The influence of metal cations on the conversion and selectivity of the reactions was assessed. We found that the salts prepared with iron and aluminum phosphomolybdate were the most effective catalysts for the esterification of levulinic acid with methanol, with the conversion and selectivity tending towards 100% after 6 h of reaction at a temperature of 323 K. The effect of catalyst loading and its recovery and reuse was evaluated; the results from the reaction using aluminum phosphomolybdate remained similar for four cycles of use. The influence of temperature on conversion and selectivity was investigated between 298 and 353 K. The reactivity of different alcohols with a carbon chain size of C1-C4 was assessed and conversions above 65% were obtained for all alcohols tested under the conditions evaluated, except for tert-butyl alcohol. These catalysts are a promising alternative to the traditional soluble and corrosive Brønsted acid catalysts. The superior performance of these catalysts was ascribed to the higher pH decline triggered by the hydrolysis of these metal cations. Full article
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Figure 1
<p>Levulinic acid synthesis from pentoses or hexoses.</p>
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<p>Effect of catalyst on the levulinic acid esterification with methyl alcohol <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), methyl alcohol (9.6 mL), catalyst (1 mol %), temperature (323 K).</p>
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<p>Curves of potentiometric titration of metal salts.</p>
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<p>Reaction pathway of esterification of acid levulinic with alkyl alcohol catalyzed by H<sup>+</sup> cations generated in the hydrolysis of metal cation present in the phosphomolybdate salt catalyst [<a href="#B43-processes-12-02574" class="html-bibr">43</a>].</p>
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<p>Conversion and methyl levulinate selectivity of phosphomolybdic heteropoly acid-catalyzed esterification of levulinic acid <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), methyl alcohol (9.6 mL), catalyst (1 mol %), temperature (323 K).</p>
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<p>Impact of catalyst load on the AlMo<sub>12</sub>O<sub>40</sub>-catalyzed esterification of levulinic acid with methyl alcohol <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), methyl alcohol (9.6 mL), catalyst (variable, temperature (323 K).</p>
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<p>Effect of catalyst load on the FeMo<sub>12</sub>O<sub>40</sub>-catalyzed esterification of levulinic acid with methyl alcohol <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), methyl alcohol (9.6 mL), catalyst (variable, temperature (323 K).</p>
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<p>Effect of catalyst load on the H<sub>3</sub>Mo<sub>12</sub>O<sub>40</sub>-catalyzed esterification of levulinic acid with methyl alcohol <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), methyl alcohol (9.6 mL), catalyst (variable, temperature (323 K).</p>
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<p>Effect of temperature on the kinetic curves of the AlMo<sub>12</sub>O<sub>40</sub>-catalyzed esterification of levulinic acid with methyl alcohol <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), methyl alcohol (9.6 mL), catalyst (1 mol %), temperature (variable).</p>
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<p>Impact of temperature on the kinetic curves of the FeMo<sub>12</sub>O<sub>40</sub>-catalyzed esterification of levulinic acid with methyl alcohol <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), methyl alcohol (9.6 mL), catalyst (1 mol %), temperature (variable).</p>
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<p>AlMo<sub>12</sub>O<sub>40</sub>-catalyzed esterification of levulinic acid with alkyl alcohols <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), alkyl alcohol (9.6 mL), catalyst (1 mol %), temperature (323 K).</p>
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<p>Conversion of AlMo<sub>12</sub>O<sub>40</sub>, or FeMo<sub>12</sub>O<sub>40</sub>-catalyzed esterification of levulinic acid with alkyl alcohols <sup>a</sup>. <sup>a</sup> Reaction conditions: levulinic acid (4.0 mmol), alkyl alcohol (9.6 mL), catalyst (1 mol %), temperature (323 K); time (6 h).</p>
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<p>Heteropoly salt-catalyzed levulinic acid with alkyl alcohol.</p>
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<p>Tendency of the donating effect of methyl groups.</p>
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15 pages, 3074 KiB  
Article
A Case Study on Integrating an Eco-Design Tool into the Construction Decision-Making Process
by Kétlin Cornely, Guilherme Ascensão and Victor M. Ferreira
Appl. Sci. 2024, 14(22), 10583; https://doi.org/10.3390/app142210583 (registering DOI) - 16 Nov 2024
Viewed by 496
Abstract
To enhance the sustainability of construction and meet the sector’s environmental agenda, it is essential to comprehensively scrutinize the environmental, social, and economic impacts of construction projects from the project’s design stage. Such assessment is of utmost importance to minimize the impacts of [...] Read more.
To enhance the sustainability of construction and meet the sector’s environmental agenda, it is essential to comprehensively scrutinize the environmental, social, and economic impacts of construction projects from the project’s design stage. Such assessment is of utmost importance to minimize the impacts of both new construction and rehabilitation projects and is particularly critical during the selection of building materials and construction solutions. This work reports improvements in functionality and user-friendliness of an eco-design tool (UAveiroGreenBuilding) targeting the construction/rehabilitation sector and previously developed within our research group. The optimized version of the eco-design tool underwent validation through the assessment of competitive window frame materials (e.g., wood, PVC, and aluminum) for potential implementation in a rehabilitation project. Windows with PVC frames were identified as the preferred window configuration due to their superior environmental performance and favorable economic profile. Additionally, a digital communication interface was developed to connect the eco-design tool with building information modeling (BIM) projects, achieved through a routine integrated using a Dynamo application. Such successful integration not only streamlined and expedited the data transfer process by obviating the need for manual input but it also enabled the storage of environmental data throughout the life cycle of the project using a simple and reliable data storage protocol. Full article
(This article belongs to the Section Civil Engineering)
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Figure 1
<p>University of Aveiro Campus. (<b>a</b>) The red line highlights the Central Technical Area and (<b>b</b>) the plant of the Central Technical Area.</p>
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<p>Normalized environmental impact of different window frame materials.</p>
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<p>Normalized resource consumption of different window frame materials’ (<b>a</b>) consumption of non-renewable resources and (<b>b</b>) consumption of renewable resources.</p>
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<p>Economic assessment of different window frame solutions.</p>
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<p>Dynamo routine structure.</p>
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<p>Parameters entered into BIM (<b>a</b>) and imported data after executing the developed Dynamo routine (<b>b</b>).</p>
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12 pages, 1092 KiB  
Article
Clinical Efficacy of Two Different Low-Level Laser Therapies for the Treatment of Trigeminal Neuralgia: A Randomized, Placebo-Controlled Trial
by İrem Karagözoğlu, Nermin Demirkol, Özge Parlar Öz, Gökçe Keçeci, Beste Çetin and Mutlu Özcan
J. Clin. Med. 2024, 13(22), 6890; https://doi.org/10.3390/jcm13226890 (registering DOI) - 15 Nov 2024
Viewed by 238
Abstract
Background: Trigeminal neuralgia (TN) is a disease that causes severe pain that can seriously affect the quality of life. This study aimed to compare the effectiveness of two different low-level laser therapies (LLLT) as alternatives to medical treatment to reduce pain and improve [...] Read more.
Background: Trigeminal neuralgia (TN) is a disease that causes severe pain that can seriously affect the quality of life. This study aimed to compare the effectiveness of two different low-level laser therapies (LLLT) as alternatives to medical treatment to reduce pain and improve the quality of life in patients with TN. Methods: A total of 45 patients were randomly divided into 3 groups. In the first group, a new-generation diode laser (GRR laser) was applied at predetermined points in the trigeminal nerve line. In the second group, a low-level neodymium-doped yttrium aluminum garnet (Nd:YAG) laser was applied along the affected nerve line. The placebo group received the same protocol with a Nd:YAG laser without the device switched on. The scores were recorded pre- and post-treatment using the Brief Pain Inventory-Facial (BPI-facial) scale. Results: A statistically significant difference was found between the pre- and post-treatment values of all four variables in the GRR laser, Nd:YAG laser, and placebo groups. When the post-treatment values were compared, statistically significant differences were found between the groups in pain frequency, pain intensity, and interference in facial-specific activities, but no differences were found in general activities. Conclusions: Both LLLTs can be considered alternative treatment modalities for TN, but the GRR laser treatment was more effective than the Nd:YAG laser treatment in reducing pain and improving the quality of life in patients with TN. Full article
(This article belongs to the Topic Advances in Dental Health)
15 pages, 4421 KiB  
Review
Unusual Lignocellulosic Bioresins: Adhesives and Coatings for Metals and Glass
by Antonio Pizzi
Molecules 2024, 29(22), 5401; https://doi.org/10.3390/molecules29225401 (registering DOI) - 15 Nov 2024
Viewed by 540
Abstract
This minireview presents some unusual but encouraging examples of lignocellulosic-based adhesives and coatings used for metals, glass, and some other difficult-to-adhere materials. The reactions and applications presented are as follows. (i) The reactions of tannins and wood lignin with phosphate salts, in particular [...] Read more.
This minireview presents some unusual but encouraging examples of lignocellulosic-based adhesives and coatings used for metals, glass, and some other difficult-to-adhere materials. The reactions and applications presented are as follows. (i) The reactions of tannins and wood lignin with phosphate salts, in particular triethylphosphate, to adhere and join steel and aluminum to Teflon, in particular for non-stick frying pans. These adhesive coatings have been shown to sustain the relevant factory industrial test of 410 °C for 11 min and, moreover, to present a 50% material loss even at 900 °C for 5 min. (ii) Non-isocyanate polyurethanes (NIPU) based on glucose and sucrose as coatings of steel and glass. These were obtained by the carbonation of carbohydrates through reaction with the inexpensive dimethyl carbonate followed by reaction with a diamine; all materials used were bio-sourced. Lastly, (iii) the use of citric acid-based adhesive coupled with any hydroxyl groups carrying material for coating metals is also described. These three approaches give a clear indication of the possibilities and capabilities of biomaterials in this field. All these are presented and discussed. Full article
(This article belongs to the Special Issue Advances in Polymer Materials Based on Lignocellulosic Biomass)
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Figure 1

Figure 1
<p>Structure of a flavonoid unit with atom numbering.</p>
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<p>Basic structures (<b>I</b>) and (<b>II</b>) produced by the reaction of triethylphosphate on the C3 site of tannin flavonoid units [<a href="#B27-molecules-29-05401" class="html-bibr">27</a>].</p>
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<p>Basic structures (<b>III</b>) and (<b>IV</b>) produced by the reaction of triethylphosphate at the aromatic B-ring C4′ and C5′ sites of tannin flavonoid units, coupled with the reaction at the C3 site [<a href="#B27-molecules-29-05401" class="html-bibr">27</a>].</p>
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<p>Structure of a trimer of mimosa tannin showing C4–C8 linkage between the terminal and before-terminal flavonoid unit and C4–C6 linkage between the before-terminal flavonoid unit and all subsequent flavonoid units [<a href="#B2-molecules-29-05401" class="html-bibr">2</a>].</p>
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<p>A variety of structures detected in the reaction of flavonoid tannins with triethylphosphate [<a href="#B27-molecules-29-05401" class="html-bibr">27</a>].</p>
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<p>A variety of structures detected in the reaction of flavonoid tannins with triethylphosphate [<a href="#B27-molecules-29-05401" class="html-bibr">27</a>].</p>
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<p>Structure of the reaction of triethylphosphate with an aminated flavonoid tannin unit [<a href="#B27-molecules-29-05401" class="html-bibr">27</a>].</p>
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<p>Higher-molecular-weight oligomer species detected by reaction of resorcinol used as a simple model compound of aromatic rings of tannin [<a href="#B27-molecules-29-05401" class="html-bibr">27</a>].</p>
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<p>Structure of a flavonoid tannin trimer showing a number of flavonoid units where the heterocyclic ring of the structure has been cleaved and the structure is open [<a href="#B2-molecules-29-05401" class="html-bibr">2</a>].</p>
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<p>Example of TEP reaction site on lignin structure [<a href="#B32-molecules-29-05401" class="html-bibr">32</a>].</p>
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<p>An example of the variety of structures formed by the reaction of triethyl phosphate with lignin units. Note also the cyclic structures formed by intramolecular reaction [<a href="#B32-molecules-29-05401" class="html-bibr">32</a>].</p>
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<p>Example of a detected aminated lignin structure obtained by reaction with triethylphosphate [<a href="#B32-molecules-29-05401" class="html-bibr">32</a>].</p>
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<p>An example of a detected higher-molecular-weight oligomer produced by the reaction of triethylphosphate linking two lignin units [<a href="#B32-molecules-29-05401" class="html-bibr">32</a>]. Note: TEP can be linked through the phenolic –OH groups, as in the figure; with the aliphatic lignin –Ohs; or with both –OH types.</p>
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<p>(<b>Top</b>) Water contact angle variation as a function of time of the lignin-TEP-based resin coated beech wood surface and the untreated beech sample control. (<b>Bottom</b>) Water drop shape after 60 s on: (<b>a</b>) untreated beech wood (control) and (<b>b</b>) beech wood surface coated with a lignin–TEP-based resin [<a href="#B32-molecules-29-05401" class="html-bibr">32</a>].</p>
Full article ">Figure 13 Cont.
<p>(<b>Top</b>) Water contact angle variation as a function of time of the lignin-TEP-based resin coated beech wood surface and the untreated beech sample control. (<b>Bottom</b>) Water drop shape after 60 s on: (<b>a</b>) untreated beech wood (control) and (<b>b</b>) beech wood surface coated with a lignin–TEP-based resin [<a href="#B32-molecules-29-05401" class="html-bibr">32</a>].</p>
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<p>Frying pan metal base with the polyphenolic-TEP binder applied to it (<b>left</b>) and finished pan with Teflon applied on the binder according to a proprietary process (<b>right</b>) [<a href="#B33-molecules-29-05401" class="html-bibr">33</a>].</p>
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<p>Linear and branched oligomers identified in glucose-based NIPUs [<a href="#B60-molecules-29-05401" class="html-bibr">60</a>].</p>
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<p>A polymeric species identified in sucrose-based NIPUs [<a href="#B62-molecules-29-05401" class="html-bibr">62</a>].</p>
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<p>Appearance of glucose and sucrose NIPU coatings on steel. Left: sucrose NIPU coating. Right: glucose NIPU coating [<a href="#B61-molecules-29-05401" class="html-bibr">61</a>].</p>
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<p>Cross-cut test according to [<a href="#B63-molecules-29-05401" class="html-bibr">63</a>] of a glucose-based surface coating on stainless steel cured for 3 min at 300 °C. (<b>a</b>) Before washing in hot water; (<b>b</b>) after washing in hot water [<a href="#B61-molecules-29-05401" class="html-bibr">61</a>].</p>
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18 pages, 7690 KiB  
Article
A Comparison of the Microstructure and Mechanical Properties of RSW and RFSSW Joints in AA6061-T4 for Automotive Applications
by Damon Gale, Taylor Smith, Yuri Hovanski, Kate Namola and Jeremy Coyne
J. Manuf. Mater. Process. 2024, 8(6), 260; https://doi.org/10.3390/jmmp8060260 - 14 Nov 2024
Viewed by 456
Abstract
To reduce vehicle weight and improve energy efficiency, automotive manufacturers are increasingly using aluminum body panels. However, the traditional joining method, Resistance Spot Welding (RSW), presents challenges like weld porosity and electrode degradation when used with aluminum. These issues have driven the industry [...] Read more.
To reduce vehicle weight and improve energy efficiency, automotive manufacturers are increasingly using aluminum body panels. However, the traditional joining method, Resistance Spot Welding (RSW), presents challenges like weld porosity and electrode degradation when used with aluminum. These issues have driven the industry to explore alternative, more effective methods for joining aluminum in vehicle manufacturing such as Refill Friction Stir Spot Welding (RFSSW). This research reports on a comparison of the microstructure and mechanical properties of welds made with RSW and RFSSW in AA6061-T4 automotive sheets. This comparison includes CT scanning, optical and SEM imaging, statistical microscopy, hardness testing, tensile testing, and fatigue testing. The results showed that RFSSW produced fully consolidated welds with a refined, equiaxed grain structure that outperformed RSW’s dendritic grain structure by as much as 73% in tensile testing and 2600% in fatigue testing. These results suggest that future designs utilizing RFSSW could incorporate fewer joints, reducing processing time, energy consumption, and tool wear. Cost studies also found that RFSSW consumes 2.5% of the energy that RSW does per joint, demonstrating that RFSSW is positioned as the preferred method for joining aluminum automotive sheets. Full article
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Figure 1
<p>The RSW process.</p>
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<p>The four stages of RFSSW: (<b>A</b>) clamping, (<b>B</b>) plunging, (<b>C</b>) refilling, and (<b>D</b>) lifting.</p>
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<p>(<b>A</b>) Drawing of the test coupon’s width, height, and weld placement in (<b>B</b>) 2 sheet stack-ups and (<b>C</b>) 3 sheet stack-ups.</p>
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<p>Surface profiles of RFSSW and RSW.</p>
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<p>CT Scan images of 2.0 mm/2.5 mm/1.2 mm stack-up utilizing: (<b>A</b>) RFSSW, (<b>B</b>) RSW.</p>
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<p>(<b>A</b>) Locations of EBSD scans for RFSSW (<b>Top</b>) and RSW (<b>Bottom</b>); (<b>B</b>) Grain maps of RFSSW (<b>Left</b>) and RSW (<b>Right</b>) at 1000× magnification; (<b>C</b>) Grain size distribution of RFSSW (I. nugget center and II. Nugget edge) and RSW (III. Nugget center and IV. Nugget edge).</p>
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<p>Microhardness heat maps of RFFSW and RSW welds (Vickers).</p>
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<p>(<b>A</b>) Fracture modes (nugget pullout and interfacial fracture); (<b>B</b>) Difference in tensile strength between RFSSW and RSW.</p>
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<p>(<b>A</b>) Elongation at UTS for RFSSW and RSW; (<b>B</b>) SEM images at 2500× magnification of the fracture surfaces, RFSSW (ductile dimple) and RSW (brittle fraction).</p>
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<p>Fatigue life curves of RFSSW and RSW.</p>
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12 pages, 2457 KiB  
Article
Vibrational Spectroscopic Identification of the [AlCl2]+ Cation in Ether-Containing Liquid Electrolytes
by Gabriela P. Gomide, Wagner A. Alves and Andrzej Eilmes
Molecules 2024, 29(22), 5377; https://doi.org/10.3390/molecules29225377 - 14 Nov 2024
Viewed by 303
Abstract
A Raman and IR study of AlCl3-based ethereal solutions is here presented and aims at identifying the [AlCl2]+ cation, which has been so far unambiguously characterized by 27Al NMR spectrometry. To do that, experimental–theoretical vibrational spectroscopy was [...] Read more.
A Raman and IR study of AlCl3-based ethereal solutions is here presented and aims at identifying the [AlCl2]+ cation, which has been so far unambiguously characterized by 27Al NMR spectrometry. To do that, experimental–theoretical vibrational spectroscopy was so employed, and the data are interpreted successfully. As a known amount of water is added to the tetrahydrofuran (THF)-containing electrolyte, a Raman band at 271 cm−1 has its intensity increased along with the most intense band of [AlCl4], and such behavior is also seen for a band at 405 cm−1 in the IR spectra. New bands at around 420 and 400 cm−1 are observed in both Raman and IR spectra for the tetraglyme (G4)-based systems. The [AlCl2(THF)4]+ complex, in the cis and trans forms, is present in the cyclic ether, while the cis-[AlCl2(G4)]+ isomer is identified in the acyclic one. Full article
(This article belongs to the Section Electrochemistry)
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<p>Raman spectra of a 0.5 mol kg<sup>−1</sup> AlCl<sub>3</sub> solution at the region of the ν<sub>AlO</sub> and ν<sub>AlCl</sub> vibrations: (a) AlCl<sub>3</sub>-THF system; (b) AlCl<sub>3</sub>-THF:H<sub>2</sub>O system with water/salt molar ratio of 0.4.</p>
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<p>Far-IR spectra of a 0.5 mol kg<sup>−1</sup> AlCl<sub>3</sub> solution at the region of the ν<sub>AlO</sub> and ν<sub>AlCl</sub> modes: (a) AlCl<sub>3</sub>-THF system; (b) AlCl<sub>3</sub>-THF:H<sub>2</sub>O system with water/salt molar ratio equal to 0.4.</p>
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<p>Raman spectra of AlCl<sub>3</sub>/G4 solutions at the region of the ν<sub>AlO</sub> and ν<sub>AlCl</sub> vibrations: (a) 1 mol kg<sup>−1</sup>; (b) 2 mol kg<sup>−1</sup>.</p>
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<p>Far-IR spectra of AlCl<sub>3</sub>/G4 solutions at the region of the ν<sub>AlO</sub> and ν<sub>AlCl</sub> vibrations: (a) 1 mol kg<sup>−1</sup>; (b) 2 mol kg<sup>−1</sup>.</p>
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<p>AIMD-simulated Raman (<b>a</b>) and IR (<b>b</b>) spectra of AlCl<sub>n</sub> complexes with explicit THF solvent molecules.</p>
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<p>AIMD-simulated Raman (<b>a</b>) and IR (<b>b</b>) spectra of AlCl<sub>n</sub> complexes with explicit G4 solvent molecule.</p>
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<p>Calculated harmonic (a) and anharmonic (b) Raman spectrum of the [AlCl<sub>4</sub>]<sup>−</sup> anion.</p>
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12 pages, 2735 KiB  
Article
PTHF/LATP Composite Polymer Electrolyte for Solid State Batteries
by Elmira Nurgaziyeva, Gulnur Turlybay, Aigul Tugelbayeva, Almagul Mentbayeva and Sandugash Kalybekkyzy
Polymers 2024, 16(22), 3176; https://doi.org/10.3390/polym16223176 - 14 Nov 2024
Viewed by 346
Abstract
The novel crosslinked composite polymer electrolyte (CPE) was developed and investigated using polytetrahydrofuran (PTHF) and polyethyleneglycol diacrylate (PEGDA), incorporating lithium aluminum titanium phosphate (LATP) particles and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt. Composite polymer electrolytes (CPEs) for solid-state lithium-ion batteries (LIBs) were synthesized by harnessing [...] Read more.
The novel crosslinked composite polymer electrolyte (CPE) was developed and investigated using polytetrahydrofuran (PTHF) and polyethyleneglycol diacrylate (PEGDA), incorporating lithium aluminum titanium phosphate (LATP) particles and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt. Composite polymer electrolytes (CPEs) for solid-state lithium-ion batteries (LIBs) were synthesized by harnessing the synergistic effects of PTHF crosslinking and the addition of LATP ceramics, while systematically varying the film composition and LATP content. CPEs containing 15 wt% LATP (PPL15) demonstrated improved mechanical strength and electrochemical stability, achieving a high conductivity of 1.16 × 10−5 S·cm−1 at 80 °C, outperforming conventional PEO-based polymer electrolytes. The CPE system effectively addresses safety concerns and mitigates the rapid degradation typically associated with polyether electrolytes. The incorporation of PEGDA not only enhances mechanical stability but also facilitates lithium salt dissociation and ion transport, leading to a uniform microstructure free from agglomerated particles. The temperature-dependent ionic conductivity measurements indicated optimal performance at lower LATP concentrations, highlighting the impact of ceramic particle agglomeration onion transport pathways. These findings contribute to advancing solid-state battery systems toward practical application. Full article
(This article belongs to the Section Polymer Applications)
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<p>(<b>a</b>) Schematic illustration of the synthesis of methacrylated-PTHF; (<b>b</b>) FTIR Spectroscopy on polymer (α-methacrylated PTHF); (<b>c</b>) chemical reaction of the synthesis of methacrylated-PTHF.</p>
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<p>(<b>a</b>) XRD images of the prepared LATP in the form of powder and pellet; (<b>b</b>) impedance profile measured at room temperature for LATP pellet.</p>
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<p>Scheme of CPE synthesis (<b>a</b>); FTIR Spectroscopy on polymer (α-methacrylated PTHF), PEGDA, CPE (<b>b</b>); structure of coin cell (<b>c</b>).</p>
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<p>SEM images of (<b>a</b>) LATP pellet; (<b>b</b>) LATP powder; (<b>c</b>) PPL0; (<b>d</b>) PPL15.</p>
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<p>TGA of PPL CPEs (<b>a</b>); stress-strain curves of PPL CPEs (<b>b</b>).</p>
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<p>LSV curve of PPL15 CPE (<b>a</b>); Arrhenius plots for PPL CPEs with different LATP content (<b>b</b>).</p>
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17 pages, 2637 KiB  
Article
Influence of Phase Composition and Morphology on the Calcium Ion Release of Several Classical and Hybrid Endodontic Cements
by Ivanka Dimitrova, Galia Gentscheva, Ivanka Spassova and Daniela Kovacheva
Materials 2024, 17(22), 5568; https://doi.org/10.3390/ma17225568 - 14 Nov 2024
Viewed by 287
Abstract
The ability of the cement to release calcium ions, which participate in the remineralization of dentin by forming apatite which improves root canal sealing with time, is of particular importance. Five recently introduced calcium-silicate commercial dental cements were investigated with a view to [...] Read more.
The ability of the cement to release calcium ions, which participate in the remineralization of dentin by forming apatite which improves root canal sealing with time, is of particular importance. Five recently introduced calcium-silicate commercial dental cements were investigated with a view to the influence of the physicochemical characteristics on the possibility of releasing calcium ions in an aqueous medium. Two hybrid calcium-silicate cements in the form of a paste-like ready mix (BioCal® Cap and TheraCal LC) and three calcium-silicate cements consisting of two components—powder and liquid (Harvard MTA Universal, Rootdent, and BioFactor) were subjected to powder XRD, SEM, and EDS for detailed examination. The cements were immersed in water for 28 days and the phase composition and morphology of the cements before and after soaking were studied. The total calcium release for each cement was determined by ICP-OES. BioFactor and BioCal® Cap release the highest amount of calcium ions, while the lowest release is registered with Rootdent and TheraCal LC. The PDT treatment of BioFactor does not influence substantially the calcium release. The impact of the elemental and phase composition on the calcium release and calcium carbonate formation was discussed. A reciprocal relation between the aluminum content and the quantity of the released calcium has been found. Full article
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16 pages, 14457 KiB  
Article
ScAlN PMUTs Based on Flexurally Suspended Membrane for Long-Range Detection
by Shutao Yao, Wenling Shang, Guifeng Ta, Jinyan Tao, Haojie Liu, Xiangyong Zhao, Jianhe Liu, Bin Miao and Jiadong Li
Micromachines 2024, 15(11), 1377; https://doi.org/10.3390/mi15111377 - 14 Nov 2024
Viewed by 314
Abstract
Piezoelectric micromachined ultrasonic transducers (PMUTs) have been widely applied in distance sensing applications. However, the rapid movement of miniature robots in complex environments necessitates higher ranging capabilities from sensors, making the enhancement of PMUT sensing distance critically important. In this paper, a scandium-doped [...] Read more.
Piezoelectric micromachined ultrasonic transducers (PMUTs) have been widely applied in distance sensing applications. However, the rapid movement of miniature robots in complex environments necessitates higher ranging capabilities from sensors, making the enhancement of PMUT sensing distance critically important. In this paper, a scandium-doped aluminum nitride (ScAlN) PMUT based on a flexurally suspended membrane is proposed. Unlike the traditional fully clamped design, the PMUT incorporates a partially clamped membrane, thereby extending the vibration displacement and enhancing the output sound pressure. Experimental results demonstrate that at a resonant frequency of 78 kHz, a single PMUT generates a sound pressure level (SPL) of 112.2 dB at a distance of 10 mm and achieves a high receiving sensitivity of 12.3 mV/Pa. Distance testing reveals that a single PMUT equipped with a horn can achieve a record-breaking distance sensing range of 11.2 m when used alongside a device capable of simultaneously transmitting and receiving ultrasound signals. This achievement is significant for miniaturized and integrated applications that utilize ultrasound for long-range target detection. Full article
(This article belongs to the Special Issue MEMS Ultrasonic Transducers)
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<p>(<b>a</b>) Structure of the PMUT; (<b>b</b>–<b>d</b>) cross-sectional structure of FS-PMUT with sealed grooves, T-PMUT, and FS-PMUT with open grooves.</p>
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<p>(<b>a</b>) The first-order modal shapes of FS-PMUT with different numbers of grooves, including those with open grooves (top) and those with sealed grooves (bottom); (<b>b</b>) transmission sensitivity and reception sensitivity of FS-PMUT with different numbers of grooves, including those with open grooves (dashed line) and with sealed grooves (solid line); (<b>c</b>,<b>d</b>) transmission and reception sensitivity of FS-PMUT with four sealed grooves of different widths; (<b>e</b>,<b>f</b>) transmission and reception sensitivity of FS-PMUT with four sealed grooves of different angles.</p>
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<p>(<b>a</b>) Equivalent circuit model, including the electrical domain (left) and mechanical domain (right); (<b>b</b>) schematic diagram of the boundary structure.</p>
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<p>Simulated frequency responses of FS-PMUT and T-PMUT at their resonance frequencies: (<b>a</b>) mode shapes of FS-PMUT and T-PMUT; (<b>b</b>) center displacement of PMUT at 10 Vpp; (<b>c</b>) comparison of vibration displacement along the diameter direction of the PMUT. (<b>d</b>) Transmission sensitivity at a distance of 10 mm; (<b>e</b>) comparison of reception sensitivity.</p>
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<p>(<b>a</b>–<b>f</b>) FS-PMUT (sealed groove) fabrication process flow; (<b>g</b>,<b>h</b>) scanning electron microscopy of the upper surface of FS-PMUT (sealed groove).</p>
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<p>(<b>a</b>) Device dimensions (2 mm × 2 mm × 0.3 mm) relative to a coin and a conventional ultrasound transducer; (<b>b</b>–<b>d</b>) the optical images of the three PMUT structures mentioned in this work: (<b>b</b>) is FS-PMUT with sealed grooves, (<b>c</b>) is FS-PMUT with open grooves, (<b>d</b>) is T-PMUT; (<b>e</b>,<b>f</b>) the cross-sectional view taken through a scanning electron microscope.</p>
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<p>LDV test results of FS-PMUT (R590) and T-PMUT (R715). (<b>a</b>) center displacement of PMUT at 10 Vpp; (<b>b</b>) the displacement along the diameter direction of the PMUT.</p>
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<p>Measured electrical impedance values of a single PMUT in air. (<b>a</b>) electrical characteristics of FS-PMUT with sealed grooves; (<b>b</b>) electrical characteristics of FS-PMUT with open grooves; (<b>c</b>) electrical characteristics of T-PMUT.</p>
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<p>(<b>a</b>) Schematic diagram of experimental set up; (<b>b</b>–<b>d</b>) comparison results of the reception sensitivity.</p>
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<p>(<b>a</b>) The block diagram of the system; (<b>b</b>) experimental assembly for distance testing; (<b>c</b>) envelope curves of the echo signal during distance measurement using a single PMUT.</p>
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<p>SNR versus distance: at a threshold of 12 dB, the maximum range of the FS-PMUT with sealed grooves is 11.2 m.</p>
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17 pages, 2151 KiB  
Article
Design and Development of D-A-D Organic Material for Solution-Processed Organic/Si Hybrid Solar Cells with 17.5% Power Conversion Efficiency
by Fahim Ullah, Kamran Hasrat, Sami Iqbal and Shuang Wang
Molecules 2024, 29(22), 5369; https://doi.org/10.3390/molecules29225369 - 14 Nov 2024
Viewed by 251
Abstract
Organic/silicon hybrid solar cells have attracted much interest due to their cheap fabrication process and simple device structure. A category of organic substances, Dibenzothiophene–Spirobifluorene–Dithiophene (DBBT-mTPA-DBT), comprises dibenzo [d,b] thiophene and 3-(3-methoxyphenyl)-6-(4-methoxyphenyl)-9H-Carbazole, which function as electron donors. In contrast, methanone is an [...] Read more.
Organic/silicon hybrid solar cells have attracted much interest due to their cheap fabrication process and simple device structure. A category of organic substances, Dibenzothiophene–Spirobifluorene–Dithiophene (DBBT-mTPA-DBT), comprises dibenzo [d,b] thiophene and 3-(3-methoxyphenyl)-6-(4-methoxyphenyl)-9H-Carbazole, which function as electron donors. In contrast, methanone is an electron acceptor, with an ∆Est of 3.19 eV. This work focused on hybrid solar cells based on the guest–host phenomena of DBBT-mTPA-DBT and CBP. Using a Si/poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT: PSS) hybrid solar cell with an ultra-thin Dibenzothiophene–Spirobifluorene–Dithienothiophene (DBBT-mTPA-DBT) interlayer between Si and Al led to a PCE of 17.5 ± 2.5%. The DBBT-mTPA-DBT interlayer substantially improved the Si/Al interface, reducing contact resistance from 6.5 × 10⁻1 Ω·cm2 to 3.5 × 10⁻2 Ω·cm2. This improvement increases electron transport efficiency from silicon to aluminum and reduces carrier recombination. The solar cell containing the DBBT-mTPA-DBT/Al double-layer cathode shows a 10.85% increase in power conversion efficiency relative to the standard Al cathode device. Full article
(This article belongs to the Special Issue Catalysts: New Materials for Green Chemistry)
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<p>(<b>a</b>) J-V characteristics of hybrid solar cells with and without DBBT-mTPA-DBT layer manufactured under identical circumstances and tested under AM 1.5 light irradiation at 100 mW/cm<sup>2</sup>; (<b>b</b>) EQE spectra; (<b>c</b>) the relationship between reflectivity and wavelength of the device with Si and Si/PEDOT: PSS; and (<b>d</b>) IQE<sup>−1</sup> plotted in absorption lengths of the device with and W/O DBBT-mTPA-DBT layer.</p>
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<p>(<b>a</b>) Al rear Si current–voltage measurements with and without DBBT-mTPA-DBT layer; (<b>b</b>) scheme for measuring contact resistance, R1, R2, R3 is resistance between contact and <span class="html-italic">W</span> and <span class="html-italic">d</span> is the contact length and width respectively; and (<b>c</b>) extrapolated series resistance <span class="html-italic">R<sub>s</sub></span> values from dV/d (lnI) vs. “I” of hybrid solar cells with and without DBBT-mTPA-DBT.</p>
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<p>(<b>a</b>) Band diagram of PEDOT:PSS/Si heterojunction hybrid solar cells. (<b>b</b>) Schematic diagram of the Si/PEDOT: PSS hybrid solar cells.</p>
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<p>Molecular structure and synthetic method of DBBT-mTPA-DBT.</p>
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<p>(<b>a</b>) Chemical structure, HOMO and LUMO electron cloud distribution, and (<b>b</b>) energy gap of DBBT-mTPA-DBT.</p>
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<p>(<b>a</b>,<b>b</b>) indicate absorption and emission peaks spotted at 347 and 550 nm of DBBT-mTPA-DBT. (<b>c</b>) Pl spectra of DBBT-mTPA-DBT at different states. (<b>d</b>) TGA trace of DBBT-mTPA-DBT with a heating rate of 10 °C min<sup>−1</sup>.</p>
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<p>(<b>A</b>) The chemical structure of CBP; (<b>B</b>) different guest–host molar ratios ranging from 0 to 90%.</p>
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37 pages, 6444 KiB  
Review
The Role of Precipitates in Hydrogen Embrittlement of Precipitation-Hardenable Aluminum Alloys
by Terezie Košová Altnerová, Darja Rudomilova, Pavel Novák and Tomáš Prošek
Metals 2024, 14(11), 1287; https://doi.org/10.3390/met14111287 - 14 Nov 2024
Viewed by 309
Abstract
This review examines hydrogen embrittlement (HE) in precipitation-hardenable aluminum alloys, focusing on the role of precipitates as hydrogen traps. It covers hydrogen entry mechanisms, the effects of microstructural features such as dislocations and grain boundaries, and secondary phase evolution during heat treatment. The [...] Read more.
This review examines hydrogen embrittlement (HE) in precipitation-hardenable aluminum alloys, focusing on the role of precipitates as hydrogen traps. It covers hydrogen entry mechanisms, the effects of microstructural features such as dislocations and grain boundaries, and secondary phase evolution during heat treatment. The interaction between hydrogen and precipitates, including the role of coherent and incoherent interfaces, is analyzed in view of the impact on HE susceptibility. Various techniques used to assess the interaction between hydrogen and aluminum alloys are also compared. The goal is to summarize the state-of-the-art understanding of the microstructural factors influencing the resistance of aluminum alloys to HE. Full article
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<p>Schematic drawing of trap sites in metals.</p>
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<p>Microstructure of Al-2 wt.% Cu age-hardened alloy.</p>
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<p>Schematic illustration of: (<b>a</b>) solid solution, (<b>b</b>) coherent precipitate, (<b>c</b>) semi-coherent precipitate, and (<b>d</b>) incoherent precipitate. Different size dots indicate different types of atoms.</p>
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<p>Schematic diagram of hydride formation mechanism. Reprinted with permission from ref. [<a href="#B67-metals-14-01287" class="html-bibr">67</a>], 1989 Elsevier Science Publishing. (<b>a</b>) The movement of hydrogen toward areas of elevated hydrostatic stress in front of crack tips. (<b>b</b>) Formation of brittle hydride. (<b>c</b>) Hydride fracture followed by blunting at the hydride/matrix interface.</p>
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<p>Schematic diagram of Hydrogen-Enhanced Decohesion mechanism. Three types of weakening of the interatomic bond (1) by hydrogen in the lattice (2) by adsorbed hydrogen (3) by hydrogen at the particle/matrix interface. Adapted from Ref. [<a href="#B11-metals-14-01287" class="html-bibr">11</a>].</p>
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<p>Schematic diagram of Hydrogen-Enhanced Localized Plasticity mechanism. Adapted from Ref. [<a href="#B11-metals-14-01287" class="html-bibr">11</a>].</p>
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<p>Schematic diagram of Adsorption-Induced Dislocation Emission mechanism. Reprinted with permission from ref. [<a href="#B67-metals-14-01287" class="html-bibr">67</a>], 1989 Elsevier Inc.</p>
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<p>Schematic illustration of aging states of aluminum alloys.</p>
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<p>HRTEM image of S phase particle (Al<sub>2</sub>CuMg) of AA 2024-T3 exposed in 0.01 M NaCl solution for 30 min. Reprinted with permission from ref. [<a href="#B123-metals-14-01287" class="html-bibr">123</a>]. 2020 Elsevier Ltd.</p>
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<p>TEM (bright field) images of AA 6063 in: (<b>a</b>) under-aged, (<b>b</b>) peak-aged, and (<b>c</b>) over-aged conditions. Adapted from Ref. [<a href="#B104-metals-14-01287" class="html-bibr">104</a>].</p>
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<p>Imaging of hydrogen trapped in a sample of AA 6061-T6 charged with hydrogen using both two-dimensional (2D) and three-dimensional (3D) secondary ion mass spectrometry (SIMS). Reprinted with permission from ref. [<a href="#B20-metals-14-01287" class="html-bibr">20</a>], 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. (<b>A</b>) 2D images of <sup>1</sup>H<sup>−</sup>, and <sup>28</sup>Si<sup>−</sup>, <sup>52</sup>Cr<sup>−</sup>, <sup>56</sup>Fe<sup>−</sup> (<b>B</b>) 3D image of <sup>1</sup>H<sup>−</sup> (<b>C</b>) 3D image of <sup>1</sup>H<sup>−</sup> after TDA measurement.</p>
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<p>Changes in equilibrium fraction of precipitating phases in AA 7050 in relation to temperature; H: homogenization temperature, 1 to 5: various quenching temperatures. Reprinted with permission from ref. [<a href="#B108-metals-14-01287" class="html-bibr">108</a>], 2004 Elsevier B.V.</p>
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<p>Fracture surface of the 7050 aluminum alloy in three different states: (<b>a</b>) in air, (<b>b</b>) precharged with hydrogen for 12 h, and (<b>c</b>) 24 h. Reprinted from ref. [<a href="#B41-metals-14-01287" class="html-bibr">41</a>], 2015 ASM International.</p>
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<p>Schematic illustrations of different hydrogen diffusion in AA 7046-T4: (<b>a</b>) without and (<b>b</b>) with intragranular η-MgZn<sub>2</sub> precipitates (red dots). Reprinted with permission from ref. [<a href="#B59-metals-14-01287" class="html-bibr">59</a>], 2022 Elsevier B.V.</p>
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<p>Stress-strain curves of: (<b>a</b>) under-aged, (<b>b</b>) peak-aged, and (<b>c</b>) over-aged condition of AA 7050 with different charging times. Reprinted from ref. [<a href="#B41-metals-14-01287" class="html-bibr">41</a>], 2015 ASM International.</p>
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<p>TEM images of Al–Li alloy 8090 at different stages of aging at 190 °C: (<b>A</b>) after 1.5 h, (<b>B</b>) 10 h, (<b>C</b>) 40 h, and (<b>D</b>) 100 h. Reprinted with permission from ref. [<a href="#B157-metals-14-01287" class="html-bibr">157</a>], 2014 Elsevier Inc.</p>
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<p>A general summary of the behavior of precipitates towards hydrogen during their evolution.</p>
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20 pages, 11818 KiB  
Article
Destructive Effects of Slag from Municipal Waste Incineration Plants on Cement Composites
by Marta Sybis, Jacek Mądrawski, Wojciech Kostrzewski, Emilia Konował, Zbigniew Walczak and Ireneusz Laks
Materials 2024, 17(22), 5559; https://doi.org/10.3390/ma17225559 - 14 Nov 2024
Viewed by 281
Abstract
The increasing production of solid waste and the scarcity of natural aggregates as a matter of fact have made waste recycling a necessity. One such waste, which is generated in large quantities, is slag. However, slag from incineration plants may contain harmful elements [...] Read more.
The increasing production of solid waste and the scarcity of natural aggregates as a matter of fact have made waste recycling a necessity. One such waste, which is generated in large quantities, is slag. However, slag from incineration plants may contain harmful elements that adversely affect the physical, chemical and mechanical properties of cement composites. This study presents laboratory research results on the effect of slag from the Poznan Municipal Waste Thermal Conversion Plant (Poland) on the physicochemical properties of cement composites. The samples were analyzed by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). It was shown that the slag analyzed contained significant amounts of aluminum, which had a direct effect on the structure of the concrete. An example of this influence is the release of hydrogen during reactions, which causes swelling and cracking of the concrete and reduces its mechanical strength. The authors emphasize that waste aggregate (slag) can be effectively used in the production of concrete after appropriate processing that reduces the risk of adverse effects. Full article
(This article belongs to the Section Construction and Building Materials)
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<p>Material composition of coarse slag.</p>
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<p>Slag grain size curve.</p>
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<p>(<b>a</b>) Average element composition of slag from OES analysis. (<b>b</b>) Elemental composition of the slag as determined by SEM/EDS microscopy (EDS-mapping). (<b>c</b>) Diffractogram for slag.</p>
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<p>(<b>a</b>) Average element composition of slag from OES analysis. (<b>b</b>) Elemental composition of the slag as determined by SEM/EDS microscopy (EDS-mapping). (<b>c</b>) Diffractogram for slag.</p>
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<p>Elemental EDS analysis of cement.</p>
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<p>Scheme of the test rig for testing the content of emitted gas.</p>
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<p>Cumulative gas emissions and daily gas increments from sample A.</p>
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<p>Elemental EDS analysis of sample C.</p>
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<p>Diffractogram of sample C.</p>
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<p>SEM photo of sample C.</p>
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<p>Elemental EDS analysis of sample B.</p>
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<p>Diffractogram of sample B.</p>
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<p>SEM image of sample B.</p>
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<p>XPS spectra for sample C.</p>
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<p>XPS spectra for sample B.</p>
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<p>FT-IR spectra for samples B and C.</p>
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<p>Swollen beam (<b>a</b>), and cracks in concrete specimen (<b>b</b>) caused by SOK slag supplements.</p>
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<p>EDS analysis of the swollen portion of the sample.</p>
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<p>Image of SEM of part of the concrete expansion sample.</p>
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