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Search Results (3,996)

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22 pages, 513 KiB  
Article
Blackcurrant Pomace Extract as a Natural Antioxidant in Vienna Sausages Reformulated by Replacement of Pork Backfat with Emulsion Gels Based on High Oleic Sunflower and Flaxseed Oils
by Nicoleta Cîrstea (Lazăr), Violeta Nour, Alexandru Radu Corbu and Georgiana Gabriela Codină
Gels 2024, 10(8), 534; https://doi.org/10.3390/gels10080534 - 13 Aug 2024
Viewed by 269
Abstract
The incorporation of a blackcurrant pomace extract (BPE) at 2.5%, 5.0% and 10.0% into an emulsion gel based on high oleic sunflower and linseed oils was examined in order to obtain a functional ingredient to be used as a pork backfat replacer in [...] Read more.
The incorporation of a blackcurrant pomace extract (BPE) at 2.5%, 5.0% and 10.0% into an emulsion gel based on high oleic sunflower and linseed oils was examined in order to obtain a functional ingredient to be used as a pork backfat replacer in Vienna sausages. The replacement of the pork backfat with the control emulsion gel reduced the cooking loss but negatively affected the color by decreasing L* and a* values as compared with the traditional product. A decrease in the n-6/n-3 ratio from 10.99 to around 1.54 (by 7 times) was achieved through reformulation, while the PUFA/SFA ratio increased from 0.49 to 1.09. The incorporation of BPE did not have a major impact on the fatty acid profile and improved color by increasing redness, but negatively affected the texture by increasing hardness, gumminess and share force as compared with the sausages reformulated without extract. BPE reduced the pH and the thermal stability of the emulsion gels, increased cooking loss and decreased moisture retention in sausages. BPE increased the oxidative stability of Vienna sausages enriched in polyunsaturated fatty acids; however, the incorporation of BPE into the emulsion gels above 5% affected the sensory scores for appearance, texture and general acceptability of the reformulated sausages. Full article
(This article belongs to the Special Issue Food Gels: Structure and Properties)
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19 pages, 4472 KiB  
Article
Inhaled Ivermectin-Loaded Lipid Polymer Hybrid Nanoparticles: Development and Characterization
by Seyedeh Negin Kassaee, Godwin A. Ayoko, Derek Richard, Tony Wang and Nazrul Islam
Pharmaceutics 2024, 16(8), 1061; https://doi.org/10.3390/pharmaceutics16081061 - 12 Aug 2024
Viewed by 230
Abstract
Ivermectin (IVM), a drug originally used for treating parasitic infections, is being explored for its potential applications in cancer therapy. Despite the promising anti-cancer effects of IVM, its low water solubility limits its bioavailability and, consequently, its biological efficacy as an oral formulation. [...] Read more.
Ivermectin (IVM), a drug originally used for treating parasitic infections, is being explored for its potential applications in cancer therapy. Despite the promising anti-cancer effects of IVM, its low water solubility limits its bioavailability and, consequently, its biological efficacy as an oral formulation. To overcome this challenge, our research focused on developing IVM-loaded lipid polymer hybrid nanoparticles (LPHNPs) designed for potential pulmonary administration. IVM-loaded LPHNPs were developed using the emulsion solvent evaporation method and characterized in terms of particle size, morphology, entrapment efficiency, and release pattern. Solid phase characterization was investigated by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). Using a Twin stage impinger (TSI) attached to a device, aerosolization properties of the developed LPHNPs were studied at a flow rate of 60 L/min, and IVM was determined by a validated HPLC method. IVM-loaded LPHNPs demonstrated spherical-shaped particles between 302 and 350 nm. Developed formulations showed an entrapment efficiency between 68 and 80% and a sustained 50 to 60% IVM release pattern within 96 h. Carr’s index (CI), Hausner ratio (HR), and angle of repose (θ) indicated proper flowability of the fabricated LPHNPs. The in vitro aerosolization analysis revealed fine particle fractions (FPFs) ranging from 18.53% to 24.77%. This in vitro study demonstrates the potential of IVM-loaded LPHNPs as a delivery vehicle through the pulmonary route. Full article
(This article belongs to the Special Issue Novel Dry Powder Formulation and Delivery Systems)
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<p>A schematic diagram of preparation process of LPHNPs.</p>
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<p>Particle size distribution of the developed formulations (<b>A</b>) before freeze-drying and (<b>B</b>) after freeze-drying (mean ± SD; <span class="html-italic">n</span> = 3).</p>
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<p>SEM images of the developed NPs (<b>A</b>,<b>B</b>) before and (<b>C</b>,<b>D</b>) after freeze-drying.</p>
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<p>Release profile of IVM from the prepared LPHNPs over 96 h and initial release in the first 4 h presented in top right corner.</p>
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<p>DSC thermograms of (a) pure IVM, (b) blank LPHNPs, and (c–g) IVM-loaded LPHNPs F1–F5 (exothermic up).</p>
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<p>TGA thermograms of pure IVM, blank LPHNPs, and IVM-loaded LPHNPs (F1–F5).</p>
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<p>FTIR spectra of (a) pure IVM, (b) blank LPHNPs, and (c–g) IVM-loaded LPHNPs F1–F5.</p>
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<p>XRD patterns of (<b>A</b>) pure IVM, (<b>B</b>) PCL, lecithin, Pluronic F127 (poloxamer), and IVM-loaded LPHNPs.</p>
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18 pages, 5729 KiB  
Article
Research on the Prediction of Optimal Frequency for Vibration Mixing and Comparison on Initial Performance of Cold-Recycled Asphalt Emulsion Mixture
by Tian Chen
Materials 2024, 17(16), 4003; https://doi.org/10.3390/ma17164003 - 12 Aug 2024
Viewed by 254
Abstract
The multicomponent cold-recycled asphalt emulsion mixture (CRAEM) has the ability of antireflection cracking between the base and the bottom surface layer, but it has secondary compaction and residual void, which is not conducive to crack resistance and fatigue performance. The application of high-frequency [...] Read more.
The multicomponent cold-recycled asphalt emulsion mixture (CRAEM) has the ability of antireflection cracking between the base and the bottom surface layer, but it has secondary compaction and residual void, which is not conducive to crack resistance and fatigue performance. The application of high-frequency vibration mixing technology can reduce voids and improve crack resistance, but it is limited by the complexity of testing to determine the optimal mixing frequency. The fractal dimension of gradation is deduced by fractal theory, and the prediction model for optimal frequency is proposed. Dry, wet, freeze–thaw splitting tests, and rutting tests were employed to test the early mechanical properties of high-frequency vibration mixing specimens corresponding to different vibration accelerations, and mercury inclusion tests were utilized to compare the void distribution corresponding to the optimal mixing frequency and forced mixing, and to verify the prediction model for optimal frequency. The results indicate that the high-frequency vibration mixing technology is able to benefit the initial cracking resistance (28.1% increase), moisture stability (11.2% increase), and high-temperature stability on the macro level on the optimal frequency. Meanwhile, the void distribution structure can be optimized, reducing the proportion of harmful voids and increasing the proportion of transitional pores on the micro level. However, the freeze–thaw resistance needs to be further studied. This study reduces the number and cost of experiments to determine the optimal frequency, and provides theoretical guidance and technical support for the engineering application of the CRAEM. Full article
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<p>Pavement distress with CRAEM base layer.</p>
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<p>The determination of optimal moisture content.</p>
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<p>The optimum dosage of asphalt emulsion.</p>
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<p>Mixing procedures of all the components.</p>
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<p>The appearance and internal structure of vibration mixing instrument.</p>
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<p>Splitting test device.</p>
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<p>The double logarithmic coordinate diagram between gradation and particle size.</p>
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<p>The correlation of gradation fractal dimension and optimum frequency of vibration mixing.</p>
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<p>The gradation fractal dimension of CRAEM.</p>
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<p>Indirect tensile strength under different vibration frequencies.</p>
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<p>Comparative study on the moisture stability under different vibration frequencies.</p>
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<p>Comparison of freeze–thaw tensile strength ratio under different vibration frequencies.</p>
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<p>Comparative study on dynamic stability under different vibration frequencies.</p>
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<p>Comparison on void size distribution between FM and VM (45 Hz).</p>
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16 pages, 14227 KiB  
Article
Optimizing the Extraction of Protein from Defatted Schizochytrium Cell Residues and Studying the Emulsification Characteristics of Protein
by Yingying Yang, Xiangying Zhao, Liping Liu, Xinyu Wang, Ruiguo Li and Jiaxiang Zhang
Fermentation 2024, 10(8), 416; https://doi.org/10.3390/fermentation10080416 - 11 Aug 2024
Viewed by 472
Abstract
In this study, proteins were prepared from Schizochytrium pombe residue after oil extraction using isoelectric point precipitation, and their physicochemical and emulsifying properties were investigated. Our objective was to assess the suitability of these proteins for functional ingredient applications. Through a one-way experiment and [...] Read more.
In this study, proteins were prepared from Schizochytrium pombe residue after oil extraction using isoelectric point precipitation, and their physicochemical and emulsifying properties were investigated. Our objective was to assess the suitability of these proteins for functional ingredient applications. Through a one-way experiment and optimization using response surface design, the effects of time, temperature, pH, and the material–liquid ratio of NaOH alkaline extraction were explored. The isoelectric point is verified by isoelectric point precipitation; the results revealed that crude protein from Schizochytrium (SCP) is minimally soluble at pH 4.2. Compared with whey protein (WP), it promotes better emulsion stability through the emulsification test. This study suggests that Schizochytrium oil-processing byproducts represent a promising source of protein, with potential applications as functional ingredients, offering implications for the usage of these byproducts in various industries. Full article
(This article belongs to the Section Microbial Metabolism, Physiology & Genetics)
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<p>Optimization of single-factor experiments for alkaline leaching of DOS proteins: (<b>a</b>) effect of pH on protein extraction rate; (<b>b</b>) effect of temperature on protein extraction rate; (<b>c</b>) effect of solid–liquid ratio on protein extraction rate; (<b>d</b>) effect of time on protein extraction rate. Different lowercase letters in the diagram suggest significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Response surface and contour plots for each factor. Temperature (A), pH (B), and time (C) response surface plots (<b>a</b>,<b>c</b>,<b>e</b>) and contour plots (<b>b</b>,<b>d</b>,<b>f</b>).</p>
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<p>Effect of acid precipitation conditions on SCP precipitation rate and content: (<b>a</b>) effect of acid precipitation pH on SCP precipitation rate and content; (<b>b</b>) effect of acid precipitation temperature on precipitation rate and content of SCP.</p>
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<p>Effect of SCP solution concentration and pH on the interfacial tension of oil and water: (<b>a</b>) variation in interfacial tension at the oil–water interface with time for different SCP protein concentrations (0.1–2% <span class="html-italic">w</span>/<span class="html-italic">v</span>) and WP (0.6% and 1.5% <span class="html-italic">w</span>/<span class="html-italic">v</span>); (<b>b</b>) interfacial tension of SCP at pH 3.0–9.0.</p>
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<p>EAI and ESI: (<b>a</b>) EAI and ESI at different concentrations of SCP (0.1–2% <span class="html-italic">w</span>/<span class="html-italic">v</span>) and WP (0.6% and 1.5% <span class="html-italic">w</span>/<span class="html-italic">v</span>); (<b>b</b>) EAI and ESI of SCP at different pH (3–9) conditions. WP 1 refers to a WP emulsion with a protein concentration of 0.6%, and WP 2 refers to a WP emulsion with a protein concentration of 1.5%.</p>
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<p>Mean emulsion droplet diameters (D<sub>4,3</sub>): (<b>a</b>) Mean droplet diameters of emulsions (D<sub>4,3</sub>) with different concentrations of SCP (0.1–2% <span class="html-italic">w</span>/<span class="html-italic">v</span>) and WP (0.6% and 1.5% <span class="html-italic">w</span>/<span class="html-italic">v</span>). (<b>b</b>) Mean droplet diameters of SCP emulsions (D<sub>4,3</sub>) at different pH (3–9). WP 1 refers to a WP emulsion with a protein concentration of 0.6% and WP 2 refers to a WP emulsion with a protein concentration of 1.5%.</p>
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<p>Micrographs of SCP emulsions at 0 and 30 days after storage: (<b>a</b>) micrographs of different concentrations of SCP (0.1–2% <span class="html-italic">w</span>/<span class="html-italic">v</span>) and WP (0.6% and 1.5% <span class="html-italic">w</span>/<span class="html-italic">v</span>) emulsions at 0 and 30 days after placement; (<b>b</b>) micrographs of SCP emulsions at different pH (3–7) at 0 and 30 days after placement.</p>
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<p>Creaming index of emulsions and appearance of SCP emulsion (after 0 h and 30 d of storage): (<b>a</b>) creaming index of emulsions and appearance of SCP (0.1–2% <span class="html-italic">w</span>/<span class="html-italic">v</span>) and WP (0.6% and 1.5% <span class="html-italic">w</span>/<span class="html-italic">v</span>) emulsions at different concentrations over a 30-day period of placement; (<b>b</b>) creaming index of emulsions and appearance of SCP emulsions at different pH (3–9) during 30 days of placement.</p>
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22 pages, 3747 KiB  
Article
Macroporous Poly(hydromethylsiloxane) Networks as Precursors to Hybrid Ceramics (Ceramers) for Deposition of Palladium Catalysts
by Jan Mrówka, Robert Kosydar, Kamil Kornaus, Janusz Partyka and Magdalena Hasik
Molecules 2024, 29(16), 3808; https://doi.org/10.3390/molecules29163808 - 11 Aug 2024
Viewed by 264
Abstract
Poly(hydromethylsiloxane) (PHMS) was cross-linked with 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane (D4Vi) in water-in-oil High Internal Phase Emulsions to form macroporous materials known as polyHIPEs. It was shown that in the process of pyrolysis under Ar atmosphere at 520 °C, the obtained polyHIPEs were converted [...] Read more.
Poly(hydromethylsiloxane) (PHMS) was cross-linked with 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane (D4Vi) in water-in-oil High Internal Phase Emulsions to form macroporous materials known as polyHIPEs. It was shown that in the process of pyrolysis under Ar atmosphere at 520 °C, the obtained polyHIPEs were converted to ceramers with high yields (82.8–88.0 wt.%). Structurally, the obtained ceramers were hybrid ceramics, i.e., they consisted of Si-O framework and preserved organic moieties. Macropores present in the polyHIPE precursors remained in ceramers. Ceramers contained also micro- and mesopores which resulted from the precursor’s mass loss during pyrolysis. Total pore volume and BET specific surface area related to the existence of micro- and mesopores in ceramers depended on the PHMS: D4Vi ratio applied in polyHIPE synthesis. The highest total pore volume (0.143 cm3/g) and specific surface area (344 m2/g) were reached after pyrolysis of the precursor prepared with the lowest amount of D4Vi as compared to PHMS. The composite materials obtained after deposition of PdO nanoparticles onto ceramers followed by reduction of PdO by H2 were active and selective catalysts for phenylacetylene hydrogenation to styrene. Full article
(This article belongs to the Special Issue Porous Materials as Catalysts and Sorbents)
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<p>TG and DTG curves of the studied polyHIPEs. <span class="html-italic">Note:</span> for sample symbols please refer to <a href="#sec3dot2dot1-molecules-29-03808" class="html-sec">Section 3.2.1</a>.</p>
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<p>FTIR spectra of the studied polyHIPEs (P1–P3 samples) and ceramers (C1–C3 samples). <span class="html-italic">Note:</span> for sample symbols please refer to <a href="#sec3dot2dot1-molecules-29-03808" class="html-sec">Section 3.2.1</a> and <a href="#sec3dot2dot2-molecules-29-03808" class="html-sec">Section 3.2.2</a>.</p>
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<p>DRIFT spectra recorded in situ during heating of the P3 polyHIPE under Ar atmosphere.</p>
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<p>SEM images of the materials before (P1) and after (C1) pyrolysis.</p>
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<p>Void and window size distributions in the studied polyHIPEs and ceramers determined by analysis of SEM images. <span class="html-italic">Note:</span> for sample symbols please refer to <a href="#sec3dot2dot1-molecules-29-03808" class="html-sec">Section 3.2.1</a> and <a href="#sec3dot2dot2-molecules-29-03808" class="html-sec">Section 3.2.2</a>.</p>
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<p>N<sub>2</sub> adsorption/desorption isotherms of the studied ceramers. <span class="html-italic">Note:</span> for sample symbols please refer to <a href="#sec3dot2dot2-molecules-29-03808" class="html-sec">Section 3.2.2</a>.</p>
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<p>XRD diffraction patterns of the C3 ceramer and the C3_Pd material. <span class="html-italic">Note:</span> for sample symbols please refer to <a href="#sec3dot2dot2-molecules-29-03808" class="html-sec">Section 3.2.2</a>.</p>
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<p>TPR profiles of the prepared ceramer-PdO systems. <span class="html-italic">Note:</span> for sample symbols please refer to <a href="#sec3dot2dot2-molecules-29-03808" class="html-sec">Section 3.2.2</a>.</p>
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<p>Results of phenylacetylene hydrogenation catalyzed by C1_Pd, C2_Pd and C3_Pd materials treated with H<sub>2</sub> (<b>A</b>–<b>C</b>). <span class="html-italic">Note:</span> for sample symbols please refer to <a href="#sec3dot2dot2-molecules-29-03808" class="html-sec">Section 3.2.2</a>.</p>
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11 pages, 1001 KiB  
Article
Thermal Safety Study of Emulsion Explosive Matrix under the Coupled Effects of Environmental Pressure and Bubble Content with Internal Heat Source
by Yi-Bo Zhang, Qian Liu and Xiao-Cen Shi
Processes 2024, 12(8), 1677; https://doi.org/10.3390/pr12081677 - 10 Aug 2024
Viewed by 337
Abstract
Emulsion explosives have become a hot topic in various studies due to their explosive combustion characteristics and detonation performance under different environmental pressures. The thermal safety of an emulsified matrix was studied with ignition energy as the characterization. A minimum ignition energy test [...] Read more.
Emulsion explosives have become a hot topic in various studies due to their explosive combustion characteristics and detonation performance under different environmental pressures. The thermal safety of an emulsified matrix was studied with ignition energy as the characterization. A minimum ignition energy test experimental system for emulsion matrices was established in this research. The system simulated the occurrence of hot spots inside emulsion matrices using an electric heating wire. The effect of bubbles on the thermal safety of the emulsified matrix was studied by adding expanded perlite additive to the emulsified matrix. This study investigated the variation trend in the minimum ignition energy of the emulsion matrix under the coupled effect of bubbles and ambient pressure using the orthogonal experimental method. The impacts of two factors on the thermal safety of the emulsion matrix were studied at different hot-spot temperatures. Coupled analysis experiments were conducted on emulsion matrices containing 0%, 1.5%, and 3% expanded perlite under pressure environments of 1 atm, 2 atm, and 3 atm. The critical hot-spot temperature of the emulsion matrix significantly decreases with increasing bubble content at 1 atm and 2 atm pressures, as revealed by intuitive analysis and analysis of variance. However, at 3 atm of pressure, the bubble content in the emulsion matrix has no significant effect on its critical hot-spot temperature. The results show that the thermal safety of the emulsified matrix decreases with the increase in the content of expanded perlite and environmental pressure, and the influence of environmental pressure is more significant than that of the bubble content. This paper’s research content serves as a reference for a safe emulsified matrix and as an experimental basis for establishing a production line for developing new equipment. Full article
(This article belongs to the Section Energy Systems)
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<p>Schematic diagram of critical ignition energy measurement system for emulsion matrix.</p>
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12 pages, 4010 KiB  
Article
Improving Shale Stability through the Utilization of Graphene Nanopowder and Modified Polymer-Based Silica Nanocomposite in Water-Based Drilling Fluids
by Yerlan Kanatovich Ospanov, Gulzhan Abdullaevna Kudaikulova, Murat Smanovich Moldabekov and Moldir Zhumabaevna Zhaksylykova
Processes 2024, 12(8), 1676; https://doi.org/10.3390/pr12081676 - 10 Aug 2024
Viewed by 308
Abstract
Shale formations present significant challenges to traditional drilling fluids due to fluid infiltration, cuttings dispersion, and shale swelling, which can destabilize the wellbore. While oil-based drilling fluids (OBM) effectively address these concerns about their environmental impact, their cost limits their widespread use. Recently, [...] Read more.
Shale formations present significant challenges to traditional drilling fluids due to fluid infiltration, cuttings dispersion, and shale swelling, which can destabilize the wellbore. While oil-based drilling fluids (OBM) effectively address these concerns about their environmental impact, their cost limits their widespread use. Recently, nanomaterials (NPs) have emerged as a promising approach in drilling fluid technology, offering an innovative solution to improve the efficiency of water-based drilling fluids (WBDFs) in shale operations. This study evaluates the potential of utilizing modified silica nanocomposite and graphene nanopowder to formulate a nanoparticle-enhanced water-based drilling fluid (NP-WBDF). The main objective is to investigate the impact of these nanoparticle additives on the flow characteristics, filtration efficiency, and inhibition properties of the NP-WBDF. In this research, a silica nanocomposite was successfully synthesized using emulsion polymerization and analyzed using FTIR, PSD, and TEM techniques. Results showed that the silica nanocomposite exhibited a unimodal particle size distribution ranging from 38 nm to 164 nm, with an average particle size of approximately 72 nm. Shale samples before and after interaction with the graphene nanopowder WBDF and the silica nanocomposite WBDF were analyzed using scanning electron microscopy (SEM). The NP-WBM underwent evaluation through API filtration tests (LTLP), high-temperature/high-pressure (HTHP) filtration tests, and rheological measurements conducted with a conventional viscometer. Experimental results showed that the silica nanocomposite and the graphene nanopowder effectively bridged and sealed shale pore throats, demonstrating superior inhibition performance compared to conventional WBDF. Post adsorption, the shale surface exhibited increased hydrophobicity, contributing to enhanced stability. Overall, the silica nanocomposite and the graphene nanopowder positively impacted rheological performance and provided favorable filtration control in water-based drilling fluids. Full article
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<p>Schematic illustration of modified polymer-based silica nanocomposite [<a href="#B16-processes-12-01676" class="html-bibr">16</a>].</p>
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<p>SEM picture of SiO<sub>2</sub>-NPs (<b>a</b>) and graphene nanopowder (<b>b</b>).</p>
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<p>OFITE 800 rotational viscosimeter.</p>
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<p>OFITE HTHP filter press.</p>
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<p>OFITE dynamic linear swellmeter.</p>
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<p>FT-IR spectra of the silica nanocomposite.</p>
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<p>PSD analysis of the diluted silica nanocomposite.</p>
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<p>TEM image of the diluted silica nanocomposite.</p>
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<p>FESEM micrograph of WBDF: (<b>a</b>) the base WBDF; (<b>b</b>) the silica nanocomposite WBDF; (<b>c</b>) graphene nanopowder WBDF.</p>
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17 pages, 571 KiB  
Review
Advances in Cyclodextrins and Their Derivatives in Nano-Delivery Systems
by Xin-Yu Ji, Yi-Xuan Zou, Han-Fang Lei, Yong Bi, Rui Yang, Ji-Hui Tang and Qing-Ri Jin
Pharmaceutics 2024, 16(8), 1054; https://doi.org/10.3390/pharmaceutics16081054 - 9 Aug 2024
Viewed by 330
Abstract
The diversity of cyclodextrins and their derivatives is increasing with continuous research. In addition to monomolecular cyclodextrins with different branched chains, cyclodextrin-based polymers have emerged. The aim of this review is to summarize these innovations, with a special focus on the study of [...] Read more.
The diversity of cyclodextrins and their derivatives is increasing with continuous research. In addition to monomolecular cyclodextrins with different branched chains, cyclodextrin-based polymers have emerged. The aim of this review is to summarize these innovations, with a special focus on the study of applications of cyclodextrins and their derivatives in nano-delivery systems. The areas covered include nanospheres, nano-sponges, nanogels, cyclodextrin metal–organic frameworks, liposomes, and emulsions, providing a comprehensive and in-depth understanding of the design and development of nano-delivery systems. Full article
(This article belongs to the Special Issue Cyclodextrins and Associated Nanomaterials for Drug and Gene Delivery)
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<p>Advances in CDs and their derivatives in nano-delivery systems.</p>
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18 pages, 3365 KiB  
Article
Sea Bass Fish Head Broth Treated by Thermo-Ultrasonication: Improving the Nutritional Properties and Emulsion Stability
by Huanqing Lei, Xinling Liu, Wei Zhao, Songyi Lin, Jiawei Lin, Jian Li, Xinan Zeng and Zhong Han
Foods 2024, 13(16), 2498; https://doi.org/10.3390/foods13162498 - 8 Aug 2024
Viewed by 459
Abstract
This work investigated the underlying mechanism of thermo-ultrasonic treatment to improve the nutritional properties and emulsion stability of sea bass fish head broth. The effects of ultrasonication on the processing of fish broth were compared with boiling water treatment. The nutritional properties of [...] Read more.
This work investigated the underlying mechanism of thermo-ultrasonic treatment to improve the nutritional properties and emulsion stability of sea bass fish head broth. The effects of ultrasonication on the processing of fish broth were compared with boiling water treatment. The nutritional properties of fish broth mainly include protein, fat, total sugar, 5′-nucleotide and free amino acid content. To achieve a similar effect of nutrient extraction, the thermo-ultrasonic treatment required a shorter time (30 min) than boiling water (120 min). The water-soluble protein, fat and total sugar contents were at their maximum at 120 min of the thermo-ultrasonic treatment. In particular, the fat content increased with the time of thermo-ultrasonic treatment from 0.58% to 2.70%. The emulsion structure of the fish soup was characterized by measuring its color and particle size, using optical microscopy and confocal laser scanning microscopy, and determining its storage stability. Thermo-ultrasonic treatment reduced the particle size of the fish broth emulsion and the fat globules became smaller and more homogeneous. Ultrasonication not only accelerated the nutritional and flavor content of the fish head broth, but also reduced the particle size and enhanced the stability of the emulsified system of the fish broth. The fish head tissue was more severely disrupted by the cavitation effect of an ultrasound, and nutrients migrated more and faster. This was mainly due to the cavitation and mechanical breaking force of the ultrasound on the fish head tissue and the fat globules of the fish broth. Altogether, these findings suggest that the thermo-ultrasonic treatment technique is useful for processing nutrient-rich, storage-stable and ready-to-eat fish head broth. Full article
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<p>Changes in protein (<b>A</b>), fat content (<b>B</b>) and total sugar (<b>C</b>) by boiling water and thermo-ultrasonic treatment with different treatment times (0, 30, 60, 90, 120 min). The contents and TAV of 5′-GMP (<b>D</b>), 5′-AMP (<b>E</b>) and 5′-IMP (<b>F</b>) by boiling water and thermo-ultrasonic treatment with different treatment times (0, 30, 60, 90, 120 min).</p>
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<p>Heat map of the free amino acid content of fish broth (<b>A</b>) and the breakdown of the different types of free amino acids (<b>B</b>) by boiling water and thermo-ultrasonic treatment with different treatment times (0, 30, 60, 90, 120 min).</p>
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<p><span class="html-italic">L</span>* (<b>A</b>) and d<sub>3,2</sub> (<b>B</b>) values of fish broth by different treatments and times. Droplet size distribution of fish broth by boiling water (<b>C</b>) and thermo-ultrasonic treatment (<b>D</b>) with different treatment times (1–5—0, 30, 60, 90, 120 min). The capital superscript letters (A and B) represent significant differences between treatment groups A and B, while small superscript letters (a, b, c, d, e) represent significant differences among treatment times (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Optical micrographs of fish broth prepared by boiling water (<b>A</b>) and thermo-ultrasonic treatment (<b>B</b>) with different treatment times (<b>1</b>–<b>5</b>—0, 30, 60, 90, 120 min; Bar = 50 μm).</p>
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<p>Confocal laser scanning micrographs of fish broth prepared by boiling water (<b>A</b>) and thermo-ultrasonic treatment (<b>B</b>) with different treatment times (<b>1</b>–<b>5</b>—0, 30, 60, 90, 120 min; Bar = 10 μm).</p>
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<p>Appearance of the fish broth after storage at 1, 3, 5, 7 days by boiling water (A) and thermo-ultrasonic treatment (B) with different treatment times (1–5—0, 30, 60, 90, 120 min).</p>
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<p>The correlation analysis of substances and droplet sizes of fish broth prepared by boiling water (<b>A</b>) and thermo−ultrasonic treatment (<b>B</b>) with different treatment times (0, 30, 60, 90, 120 min).</p>
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<p>Schematic diagram of the thermo-ultrasonic treatment on fish broth.</p>
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16 pages, 2315 KiB  
Article
Potential Use of Common Administration of Emulsion for Parenteral Nutrition and Vinpocetine: Compatibility Study and Prospect
by Szymon Tomczak, Kornelia Kaszuba, Jagoda Szkudlarek, Ludwika Piwowarczyk and Anna Jelińska
Metabolites 2024, 14(8), 439; https://doi.org/10.3390/metabo14080439 - 7 Aug 2024
Viewed by 308
Abstract
Vinpocetine (VP) is distributed after oral and intravenous administration, and its uptake in the thalamus, basal ganglia, and visual cortex. Due to poor bioavailability (~7%) and marked first-pass effect (~75%), including a short half-life (2–3 h), oral administration of VP is limited. It [...] Read more.
Vinpocetine (VP) is distributed after oral and intravenous administration, and its uptake in the thalamus, basal ganglia, and visual cortex. Due to poor bioavailability (~7%) and marked first-pass effect (~75%), including a short half-life (2–3 h), oral administration of VP is limited. It requires frequent administration of the drug to obtain a therapeutic effect. Attempts to overcome these difficulties include the use of new drug delivery systems and/or alternative routes of drug administration. One possibility is the common administration of lipid emulsion and drug using the same catheter. However, this procedure is not recommended due to potential interaction and lack of safety data. For this purpose, we checked the compatibility of VP solutions with eight commercially available parenteral nutrition admixtures, i.e., Lipoflex special, Omegaflex special, Lipoflex peri, Omegaflex peri, Kabiven, SmofKabiven, Kabiven Peripheral, and Olimel Peri N4E. Coadministration is only possible if the stability of the drug and the lipid emulsion is confirmed. The available data are scarce and only concern the incompatibility of VP with ibuprofen. Compatibility tests were carried out in simulated administration through a Y-site connector using clinical flow rates. The stability of the drug and lipid emulsion was assessed by visual inspection and measurement of pH, osmolality, particle size as mean droplet diameter (MDD) and percentage of lipids residing in globules larger than 5 µm (PFAT5), zeta potential, polydispersity index, and lipid-free parenteral nutrition admixture(PNA) turbidity. The results of the compatibility of VP with eight commercial PN admixtures showed that all lipid emulsions show different signs of destabilization. In the studied samples, particles larger than 1000 nm, a significant increase in MDD, zeta potential, and loss of homogeneity visible as an increase in the polydispersity index were observed. Most of the samples had PFAT5 above the USP limit (0.05%). Taking into account the obtained data, VP should not be administered with the studied lipid emulsions for parenteral nutrition. Full article
(This article belongs to the Special Issue Drug Metabolism and New Drug Development for Cancers)
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<p>The results of particle size measurements (mean droplet diameter).</p>
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<p>The results of polydispersity index (PDI).</p>
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<p>Lipid droplet size intensity for Lipoflex special sample (<b>left</b>) and Olimel Peri N4E (<b>right</b>).</p>
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<p>The results of zeta potential measurements.</p>
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17 pages, 3500 KiB  
Article
An Experimental Study on the Performance of Materials for Repairing Cracks in Tunnel Linings under Erosive Environments
by Wenliang Zhang, Yufeng Wang, Xiaocong Nan, Shangqu Sun, Yanhui Ma and Yankai Wu
Buildings 2024, 14(8), 2427; https://doi.org/10.3390/buildings14082427 - 6 Aug 2024
Viewed by 420
Abstract
Addressing the current lining cracking problem in coastal tunnels, this paper independently introduces a novel type of repair material for tunnel lining cracks—the composite repair material consisting of waterborne epoxy resin and ultrafine cement (referred to as EC composite repair material). Through indoor [...] Read more.
Addressing the current lining cracking problem in coastal tunnels, this paper independently introduces a novel type of repair material for tunnel lining cracks—the composite repair material consisting of waterborne epoxy resin and ultrafine cement (referred to as EC composite repair material). Through indoor testing, we have analyzed the change rule of the mass change rate, compressive strength, flexural strength, and chloride ion concentration of the repair material samples in erosive environments, with the dosage of each component in the EC composite repair material being varied. We have also investigated the working performance, mechanical properties, and microstructure of the repair material. The results of this study show that when the proportion of each component of ultrafine cement, waterborne epoxy resin, waterborne epoxy curing agent, waterborne polyurethane, defoamer, and water is 100:50:50:2.5:0.5:30, the performance of the EC composite repair material in a chloride ion-rich environment is optimal in all aspects. When the mixing ratio of each component of the EC composite repair material is as stated above, the repair material exhibits the best performance in a chloride ion erosion environment. With this ratio of components in the EC composite repair material, the fluidity, setting time, compressive strength, flexural strength, and bond strength of the repair material in a chloride ion erosion environment can meet the requirements of relevant specifications, and it is highly effective in repairing tunnel lining cracks. The polymeric film formed by the reaction between the waterborne epoxy resin emulsion and the curing agent fills the pores between the hydration products, resulting in a densely packed internal structure of EC composite repair material with enhanced erosion resistance, making it very suitable for repairing cracks in tunnel linings in erosive environments. Full article
(This article belongs to the Special Issue Characterization and Design of Cement and Concrete Materials)
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<p>Experimental model for bond strength.</p>
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<p>The effect of waterborne epoxy resin content on different properties. (<b>a</b>) Rate of mass change. (<b>b</b>) Compressive strength. (<b>c</b>) Flexural strength. (<b>d</b>) Chloride concentration.</p>
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<p>The effect of waterborne polyurethane content on different properties. (<b>a</b>) Rate of mass change. (<b>b</b>) Compressive strength. (<b>c</b>) Flexural strength. (<b>d</b>) Chloride concentration.</p>
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<p>The effect of defoamer dosage on different properties. (<b>a</b>) Mass change rate. (<b>b</b>) Compressive strength. (<b>c</b>) Flexural strength. (<b>d</b>) Chloride concentration.</p>
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<p>Compressive strength curves of EC composite repair material and CM repair material.</p>
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<p>Flexural strength curves of EC composite repair material and CM repair material.</p>
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<p>Bond strength curves of EC composite repair material and CM repair material.</p>
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<p>SEM diagrams of EC composite repair material and CM repair material. (<b>a</b>) SEM of CM repair material (8000×). (<b>b</b>) SEM of EC composite repair material (8000×). (<b>c</b>) SEM of CM repair material (30,000×). (<b>d</b>) SEM of EC composite repair material (30,000×).</p>
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11 pages, 1542 KiB  
Article
Lipid Emulsion Type and Liver Function in Parenteral Nutrition Patients: A Retrospective Study of Patients and Prescribing Practices
by Marvick Melendez, Ronelle Mitchell, Hannah Heredia, Jennifer Lloyd, Jill Taliaferro, Erin K. Beveridge and Stephen J. Ives
Nutrients 2024, 16(16), 2590; https://doi.org/10.3390/nu16162590 - 6 Aug 2024
Viewed by 430
Abstract
Parenteral nutrition (PN) is a life-sustaining method to provide adequate nutrients to patients unable to receive oral or enteral nutrition. PN typically contains a mixture of macro- and micro-nutrients, although the lipid composition has been identified as a concern for liver disease. Therefore, [...] Read more.
Parenteral nutrition (PN) is a life-sustaining method to provide adequate nutrients to patients unable to receive oral or enteral nutrition. PN typically contains a mixture of macro- and micro-nutrients, although the lipid composition has been identified as a concern for liver disease. Therefore, the study of the intravenous lipid emulsion (ILE) prescribing practices in home-based PN (HPN) patients and whether differing lipid PN alters liver function tests (LFTs) is needed. Methods: A retrospective study of monthly LFTs from a random sample of 105 adult HPN patients in the U.S. over a 6-month period was conducted. Patients were receiving olive oil/soy oil (n = 53, Clinolipid), mixed ILE (n = 39, SMOF Lipid), soy oil (SO; n = 4, Intralipid), or none (n = 7). LFTs monitored were alkaline phosphatase (ALP), alanine transaminase (ALT), aspartate transaminase (AST), and total bilirubin (T Bili). Results: No differences were observed in baseline LFTs across groups (all, p > 0.25, η2 < 0.04), nor were there differences in age, body mass index, days of PN, or mean PN volume (all, p > 0.36, η2 < 0.05). There were no significant interactions between ILE type and time (all p > 0.64, ηp2 < 0.03), no effect of ILE type (all p > 0.60, ηp2 < 0.03), and no effect of time (all p > 0.69, ηp2 < 0.01) in terms of LFTs. Average LFTs over six months were also not different between ILE types (all p > 0.30, η2 < 0.04). Conclusion: These findings suggested that patients were mostly prescribed mixed or ILE PN containing more than one lipid source and that differing ILEs in long-term HPN patients did not alter LFTs over a six-month period. Full article
(This article belongs to the Section Clinical Nutrition)
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<p>Baseline LFTs in adult home PN patients (n = 105) according to ILE type. (<b>A</b>) Alanine transaminase (ALT), (<b>B</b>) alkaline phosphatase (ALP), (<b>C</b>) aspartate transaminase (AST), and (<b>D</b>) total bilirubin (TBili). Data are individual points and box and whisker plots (median and IQR). The <span class="html-italic">p</span> values for group comparison were from analysis of variance.</p>
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<p>LFTs in adult home PN patients (n = 105) according to ILE type over time. (<b>A</b>) Alanine transaminase (ALT), (<b>B</b>) alkaline phosphatase (ALP), (<b>C</b>) aspartate transaminase (AST), (<b>D</b>) and total bilirubin (TBili). Data are mean ± 95% confidence intervals. The <span class="html-italic">p</span> values are for group comparison over time using two-way analysis of variance.</p>
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<p>The average of LFTs in adult home PN patients (n = 105) according to ILE type over the 6-month observation period. (<b>A</b>) Alanine transaminase (ALT), (<b>B</b>) alkaline phosphatase (ALP), (<b>C</b>) aspartate transaminase (AST), and (<b>D</b>) total bilirubin (TBili). Data are individual points and box and whisker plots (median and IQR). The <span class="html-italic">p</span> values for group comparison were from analysis of variance.</p>
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<p>Correlation matrix amongst the LFTs in adult home PN patients (n = 105) from baseline to the end of the six-month observation period. Alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP), and total bilirubin (TBili). Data are Spearman’s Rho correlation coefficients; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 for each bivariate relation.</p>
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34 pages, 9283 KiB  
Article
Analysis of the Impact of Cooling Lubricants on the Tensile Properties of FDM 3D Printed PLA and PLA+CF Materials
by Elvis Hozdić and Redžo Hasanagić
Polymers 2024, 16(15), 2228; https://doi.org/10.3390/polym16152228 - 5 Aug 2024
Viewed by 755
Abstract
This study investigates the impact of infill density on the mechanical properties of fused deposition modeling (FDM) 3D-printed polylactic acid (PLA) and PLA reinforced with carbon fiber (PLA+CF) specimens, which hold industrial significance due to their applications in industries where mechanical robustness and [...] Read more.
This study investigates the impact of infill density on the mechanical properties of fused deposition modeling (FDM) 3D-printed polylactic acid (PLA) and PLA reinforced with carbon fiber (PLA+CF) specimens, which hold industrial significance due to their applications in industries where mechanical robustness and durability are critical. Exposure to cooling lubricants is particularly relevant for environments where these materials are frequently subjected to cooling fluids, such as manufacturing plants and machine shops. This research aims to explore insights into the mechanical robustness and durability of these materials under realistic operating conditions, including prolonged exposure to cooling lubricants. Tensile tests were performed on PLA and PLA+CF specimens printed with varying infill densities (40%, 60%, 80%, and 100%). The specimens underwent tensile testing before and after exposure to cooling lubricants for 7 and 30 days, respectively. Mechanical properties such as tensile strength, maximum force, strain, and Young’s modulus were measured to evaluate the effects of infill density and lubricant exposure. Higher infill densities significantly increased tensile strength and maximum force for both PLA and PLA+CF specimens. PLA specimens showed an increase in tensile strength from 22.49 MPa at 40% infill density to 45.00 MPa at 100% infill density, representing a 100.09% enhancement. PLA+CF specimens exhibited an increase from 23.09 MPa to 42.54 MPa, marking an 84.27% improvement. After 30 days of lubricant exposure, the tensile strength of PLA specimens decreased by 15.56%, while PLA+CF specimens experienced an 18.60% reduction. Strain values exhibited minor fluctuations, indicating stable elasticity, and Young’s modulus improved significantly with higher infill densities, suggesting enhanced material stiffness. Increasing the infill density of FDM 3D-printed PLA and PLA+CF specimens significantly enhance their mechanical properties, even under prolonged exposure to cooling lubricants. These findings have significant implications for industrial applications, indicating that optimizing infill density can enhance the durability and performance of 3D-printed components. This study offers a robust foundation for further research and practical applications, highlighting the critical role of infill density in enhancing structural integrity and load-bearing capacity. Full article
(This article belongs to the Special Issue Mechanical and Structural Properties of Polymer Materials)
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<p>3D model of tensile-test specimens according to the ISO 527-2-2012 standard [<a href="#B36-polymers-16-02228" class="html-bibr">36</a>].</p>
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<p>Tensile-test specimens with “<span class="html-italic">Honeycomb</span>” infill pattern and 40%, 60%, 80%, and 100% infill density.</p>
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<p>The 3D printed PLA specimens tested: the strength-strain curves: (<b>a</b>) PLA tensile-tested specimens with 40% fill density—Case 1; (<b>b</b>) PLA tensile-tested specimens with 60% fill density—Case 2, (<b>c</b>) PLA tensile-tested specimens with 80% fill density—Case 3, and (<b>d</b>) PLA tensile-tested specimens with 100% fill density—Case 4. All the PLA tensile-tested specimens were not exposed to cooling lubricant.</p>
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<p>The 3D printed PLA specimens tested: the strength-strain curves: (<b>a</b>) PLA tensile-tested specimens with 40% fill density—Case 1; (<b>b</b>) PLA tensile-tested specimens with 60% fill density—Case 2, (<b>c</b>) PLA tensile-tested specimens with 80% fill density—Case 3, and (<b>d</b>) PLA tensile-tested specimens with 100% fill density—Case 4. All the PLA tensile-tested specimens were not exposed to cooling lubricant.</p>
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<p>The mechanical parameters of FDM 3D-printed PLA specimens tested that were not exposed to cooling lubricant: (<b>a</b>) average maximum force, (<b>b</b>) average Young’s modulus.</p>
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<p>The 3D printed PLA specimens tested: the strength-strain curves: (<b>a</b>) PLA tensile-tested specimens with 40% fill density—Case 5; (<b>b</b>) PLA tensile-tested specimens with 60% fill density—Case 6, (<b>c</b>) PLA tensile-tested specimens with 80% fill density—Case 7, and (<b>d</b>) PLA tensile-tested specimens with 100% fill density—Case 8. All PLA tensile-tested specimens were exposed to cooling lubricant for 7 days.</p>
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<p>The mechanical parameters of FDM 3D-printed PLA specimens tested that were exposed to cooling lubricant for 7 days: (<b>a</b>) average maximum force, (<b>b</b>) average Young’s modulus.</p>
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<p>The 3D printed PLA specimens tested: the strength-strain curves: (<b>a</b>) PLA tensile-tested specimens with 40% fill density—Case 9; (<b>b</b>) PLA tensile-tested specimens with 60% fill density—Case 10, (<b>c</b>) PLA tensile-tested specimens with 80% fill density—Case 11, and (<b>d</b>) PLA tensile-tested specimens with 100% fill density—Case 12. All the PLA tensile-tested specimens were exposed to cooling lubricant for 30 days.</p>
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<p>The mechanical parameters of FDM 3D-printed PLA specimens tested that were exposed to cooling lubricant for 30 days: (<b>a</b>) average maximum force, (<b>b</b>) average Young’s modulus.</p>
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<p>The mechanical parameters of FDM 3D-printed PLA specimens tested: (<b>a</b>) average tensile strength, (<b>b</b>) average strain.</p>
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<p>The 3D printed PLA+CF specimens tested: the strength-strain curves: (<b>a</b>) PLA+CF tensile-tested specimens with 40% fill density—Case 13; (<b>b</b>) PLA+CF tensile-tested specimens with 60% fill density—Case 14, (<b>c</b>) PLA+CF tensile-tested specimens with 80% fill density—Case 15, and (<b>d</b>) PLA+CF tensile-tested specimens with 100% fill density—Case 16. All the PLA+CF tensile-tested specimens were not exposed to cooling lubricant.</p>
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<p>The mechanical parameters of FDM 3D-printed PLA+CF specimens tested that were not exposed to cooling lubricant: (<b>a</b>) average maximum force, (<b>b</b>) average Young’s modulus.</p>
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<p>The 3D printed PLA+CF specimens tested: the strength-strain curves: (<b>a</b>) PLA+CF tensile-tested specimens with 40% fill density—Case 17; (<b>b</b>) PLA+CF tensile-tested specimens with 60% fill density—Case 18, (<b>c</b>) PLA+CF tensile-tested specimens with 80% fill density—Case 19, and (<b>d</b>) PLA+CF tensile-tested specimens with 100% fill density—Case 20. All the PLA+CF tensile-tested specimens were exposed to cooling lubricant for a period of 7 days.</p>
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<p>The 3D printed PLA+CF specimens tested: the strength-strain curves: (<b>a</b>) PLA+CF tensile-tested specimens with 40% fill density—Case 17; (<b>b</b>) PLA+CF tensile-tested specimens with 60% fill density—Case 18, (<b>c</b>) PLA+CF tensile-tested specimens with 80% fill density—Case 19, and (<b>d</b>) PLA+CF tensile-tested specimens with 100% fill density—Case 20. All the PLA+CF tensile-tested specimens were exposed to cooling lubricant for a period of 7 days.</p>
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<p>The mechanical parameters of FDM 3D-printed PLA+CF specimens tested that were exposed to cooling lubricant for a period of 7 days: (<b>a</b>) average maximum force, (<b>b</b>) average Young’s modulus.</p>
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<p>The 3D printed PLA+CF specimens tested: the strength-strain curves: (<b>a</b>) PLA+CF tensile-tested specimens with 40% fill density—Case 21; (<b>b</b>) PLA+CF tensile-tested specimens with 60% fill density—Case 22, (<b>c</b>) PLA+CF tensile-tested specimens with 80% fill density—Case 23, and (<b>d</b>) PLA+CF tensile-tested specimens with 100% fill density—Case 24. All the PLA+CF tensile-tested specimens were exposed to cooling lubricant for a period of 30 days.</p>
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<p>The 3D printed PLA+CF specimens tested: the strength-strain curves: (<b>a</b>) PLA+CF tensile-tested specimens with 40% fill density—Case 21; (<b>b</b>) PLA+CF tensile-tested specimens with 60% fill density—Case 22, (<b>c</b>) PLA+CF tensile-tested specimens with 80% fill density—Case 23, and (<b>d</b>) PLA+CF tensile-tested specimens with 100% fill density—Case 24. All the PLA+CF tensile-tested specimens were exposed to cooling lubricant for a period of 30 days.</p>
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<p>The mechanical parameters of FDM 3D-printed PLA+CF specimens tested that were exposed to cooling lubricant for a period of 30 days: (<b>a</b>) average maximum force, (<b>b</b>) average Young’s modulus.</p>
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<p>The mechanical parameters of FDM 3D-printed PLA+CF specimens tested: (<b>a</b>) average tensile strength, (<b>b</b>) average strain.</p>
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<p>Comparison of tensile strength between PLA and PLA+CF materials at different infill densities and exposure times: (<b>a</b>) not exposed to cooling lubricant, (<b>b</b>) exposed to cooling lubricant for a period of 7 days, (<b>c</b>) exposed to cooling lubricant for a period of 30 days.</p>
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<p>Comparison of strain between PLA and PLA+CF materials at different infill densities and exposure times: (<b>a</b>) not exposed to cooling lubricant, (<b>b</b>) exposed to cooling lubricant for a period of 7 days, (<b>c</b>) exposed to cooling lubricant for a period of 30 days.</p>
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<p>Comparison of strain between PLA and PLA+CF materials at different infill densities and exposure times: (<b>a</b>) not exposed to cooling lubricant, (<b>b</b>) exposed to cooling lubricant for a period of 7 days, (<b>c</b>) exposed to cooling lubricant for a period of 30 days.</p>
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<p>Comparison of tensile strength and strain between PLA and PLA+CF materials with 100% infill densities and exposure times: (<b>a</b>) average tensile strength, (<b>b</b>) average strain.</p>
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16 pages, 8936 KiB  
Article
Novel Collagen-Based Emulsions Embedded with Palmarosa Essential Oil, and Chamomile and Calendula Tinctures, for Skin-Friendly Textile Materials
by Laura Chirilă, Miruna S. Stan, Sabina Olaru, Alina Popescu, Mihaela-Cristina Lite, Doina Toma and Ionela C. Voinea
Materials 2024, 17(15), 3867; https://doi.org/10.3390/ma17153867 - 5 Aug 2024
Viewed by 475
Abstract
Skin-friendly textile materials were obtained by applying oil-in-water emulsions based on palmarosa essential oil, chamomile, and calendula tinctures onto cotton fabrics. Different formulations based on these bioactive principles incorporated in collagen as polymeric matrices were prepared and immobilized on a plain weave textile [...] Read more.
Skin-friendly textile materials were obtained by applying oil-in-water emulsions based on palmarosa essential oil, chamomile, and calendula tinctures onto cotton fabrics. Different formulations based on these bioactive principles incorporated in collagen as polymeric matrices were prepared and immobilized on a plain weave textile structure from 100% cotton. The functionalized textile materials were characterized in terms of physicochemical, mechanical, antibacterial, and biocompatibility points of view. The pH values of the prepared emulsions were in the range of 4.81–5.23 and showed no significant differences after 4 h of storage. Moreover, the addition of a higher quantity of active principles (palmarosa essential oil and plant tinctures) caused slightly lower values of acidic pH. The electrical conductivity of the obtained emulsions increased with the decrease in the oil phases in the system. The highest values were obtained for the emulsion developed with the smallest volume fraction of active principle—palmarosa essential oil and plant tinctures. The emulsion that contained the least amount of collagen and the highest number of active principles exhibited the lowest stability. The textile materials treated with synthesized emulsions exerted antibacterial effects against S. aureus and E. coli strains and did not affect keratinocyte growth, spreading, and organization, highlighting the biocompatibility of these developed skin-friendly textiles. Full article
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<p>Variation in time of the creaming index values for the emulsions containing palmarosa essential oil and plant tinctures.</p>
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<p>Representative images of Petri dishes revealing the antibacterial effect against (<b>a</b>) <span class="html-italic">E. coli</span> and (<b>b</b>) <span class="html-italic">S. aureus</span> strains, after 24 h in the presence of emulsion-treated fabrics.</p>
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<p>Fluorescence images of Live and Dead staining of human keratinocytes (HaCaT cells) grown for 24 h in the presence of extracts from emulsion-treated fabrics (R1–R6) or untreated fabrics (C). Live cells are shown in green (after staining with calcein AM solution) and dead cells are presented in red (labeled with propidium iodide solution). In parallel, cells without any fabrics were analyzed. All images were obtained with 20× objective.</p>
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<p>Organization of actin filaments (labeled in red with phalloidin-iFluor 555 reagent) in human keratinocytes (HaCaT cells) after 24 h of incubation in direct contact with emulsion-treated fabrics (R1–R6) or untreated fabrics (C). In parallel, cells without any fabrics were analyzed.</p>
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<p>Biocompatibility in terms of cell viability, nitric oxide level, and lactate (LDH) dehydrogenase evaluated on human keratinocytes (HaCaT cells) after 24 h of growth: (<b>a</b>) in the presence of fabrics extracts, and (<b>b</b>) in direct contact with the emulsion-treated fabrics. Data are calculated as mean ± standard deviation (<span class="html-italic">n</span> = 3) and normalized to HaCaT cells grown: (<b>a</b>) in the presence of extracts from untreated fabric (C—control), (<b>b</b>) in direct contact with untreated fabric (C). No significance was obtained after statistical analysis was performed between fabric extracts. * <span class="html-italic">p</span> &lt; 0.5 compared to untreated fabrics (C).</p>
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21 pages, 1852 KiB  
Review
Current Review: Alginate in the Food Applications
by Shirin Kazemzadeh Pournaki, Ricardo Santos Aleman, Mehrdad Hasani-Azhdari, Jhunior Marcia, Ajitesh Yadav and Marvin Moncada
J 2024, 7(3), 281-301; https://doi.org/10.3390/j7030016 - 5 Aug 2024
Viewed by 360
Abstract
Due to global development and increased public awareness of food’s effects on health, demands for innovative and healthy products have risen. Biodegradable and environmentally friendly polymer usage in modern food products is a promising approach to reduce the negative health and environmental effects [...] Read more.
Due to global development and increased public awareness of food’s effects on health, demands for innovative and healthy products have risen. Biodegradable and environmentally friendly polymer usage in modern food products is a promising approach to reduce the negative health and environmental effects of synthetic chemicals. Also, desirable features such as flavor, texture, shelf-life, storage condition, water holding capacity, a decrease in water activity, and an oil absorption of fried food have been improved by many polysaccharides. One of the important polymers, which is applied in the food industry, is alginate. Alginates are a safe and widely used compound in various industries, especially the food industry, which has led to innovative methods for for the improvement of this industry. Currently, different applications of alginate in stable emulsions and nano-capsules in food applications are due to the crosslinking properties of alginate with divalent cations, such as calcium ions, which have been studied recently. The main aim of this review is to take a closer look at alginate properties and applications in the food industry. Full article
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<p>Egg-box model of alginate-adding divalent cations.</p>
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<p>Block distribution of constituent monomers in alginate polymer (adapted by Pawer and Edgar, 2012) [<a href="#B17-J-07-00016" class="html-bibr">17</a>].</p>
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<p>Egg-box model of alginate proposed by Draget (2000) [<a href="#B16-J-07-00016" class="html-bibr">16</a>] with some modifications.</p>
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<p>Ionic gelling mechanisms. External gelification and internal gelification: insoluble salt (<b>a</b>) and partially soluble salt (<b>b</b>) (adapted by Helgerud et al., 2010) [<a href="#B25-J-07-00016" class="html-bibr">25</a>].</p>
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<p>Major steps of producing raw alginate from brown seaweed.</p>
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