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Search Results (1,485)

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Keywords = biocomposite

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21 pages, 9338 KiB  
Article
Study of Mechanical and Thermal Properties of Environmentally Friendly Composites from Beer Bagasse
by María Jordá-Reolid, Asunción Martínez-García, Ana Ibáñez-García, Miguel Ángel León-Cabezas and Josefa Galvañ-Gisbert
Polymers 2024, 16(20), 2916; https://doi.org/10.3390/polym16202916 - 17 Oct 2024
Abstract
The influence of bagasse fibres from beer manufacturing in mechanical, thermal, and rheological properties of three polymers (BioPE, PLA, and PP) has been studied in order to develop new environmentally friendly biocomposites for injection moulding applications. Totals of 10 wt%, 20 wt%, and [...] Read more.
The influence of bagasse fibres from beer manufacturing in mechanical, thermal, and rheological properties of three polymers (BioPE, PLA, and PP) has been studied in order to develop new environmentally friendly biocomposites for injection moulding applications. Totals of 10 wt%, 20 wt%, and 30 wt% of bagasse fibre (BSG) were added to the polymers by extrusion compounding, adding specific compatibilising additives, and injected samples were mechanically characterised by tensile, Charpy impact, and hardness tests. In addition, the fractures obtained after the impact test were observed using scanning electron microscopy (SEM) to assess the compatibility matrix filler. Characterisation of the thermal properties is also carried out by using differential scanning calorimetry (DSC) and thermogravimetry (TGA). Additionally, melt flow index of the biocomposites is also studied. An increase in the rigidity of the BioPE and PP composites was produced with the increase in BSG content, dealing with a decrease in maximum strain and impact resistance; whereas, in the filled BGS PLA biocomposites, Young’s modulus was lower than that of the PLA material, improving the ductility of the PLA-BGS formulations. Compatibilisation effect was, therefore, different in the nine developed formulations, and the BGS content also influenced their thermal, mechanical, and rheological behaviours. Full article
(This article belongs to the Special Issue Biodegradable Polymer Composites: Fabrication and Applications II)
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<p>TGA curve of BSG.</p>
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<p>FTIR profile for BSG.</p>
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<p>(<b>a</b>) Extrusion compounding equipment; (<b>b</b>) BioPE biocomposites; (<b>c</b>) PLA biocomposites; and (<b>d</b>) PP biocomposites.</p>
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<p>Injected samples of (<b>a</b>) BioPE biocomposites; (<b>b</b>) PLA biocomposites; and (<b>c</b>) PP biocomposites.</p>
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<p>DSC curves of BioPE biocomposites.</p>
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<p>DSC curves of PLA biocomposites.</p>
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<p>DSC curves of PP biocomposites.</p>
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<p>TGA curves of BioPE biocomposites.</p>
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<p>TGA curves of PLA biocomposites.</p>
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<p>TGA curves of PP biocomposites.</p>
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<p>Bar graph MFI results.</p>
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<p>Stress–strain curves for BioPE biocomposites.</p>
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<p>Stress–strain curves for PP biocomposites.</p>
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<p>Stress–strain curves for PLA biocomposites.</p>
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<p>Bar graph impact strength results.</p>
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<p>SEM micrographs of BioPE biocomposites. (<b>a</b>) BioPE90BSG10 at 100×, (<b>b</b>) BioPE90BSG10 at 500×, (<b>c</b>) BioPE80BSG20 at 100×, (<b>d</b>) BioPE80BSG20 at 500×, (<b>e</b>) BioPE70BSG30 at 100× and (<b>f</b>) BioPE70BSG30 at 500×.</p>
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<p>SEM micrographs of PLA biocomposites. (<b>a</b>) PLA90BSG10 at 100×, (<b>b</b>) PLA90BSG10 at 500×, (<b>c</b>) PLA80BSG20 at 100×, (<b>d</b>) PLA80BSG20 at 500×, (<b>e</b>) PLA70BSG30 at 100× and (<b>f</b>) PLA70BSG30 at 500×.</p>
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<p>SEM micrographs of PP biocomposites. (<b>a</b>) PP90BSG10 at 100×, (<b>b</b>) PP90BSG10 at 500×, (<b>c</b>) PP80BSG20 at 100×, (<b>d</b>) PP80BSG20 at 500×, (<b>e</b>) PP70BSG30 at 100× and (<b>f</b>) PP70BSG30 at 500×.</p>
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16 pages, 2800 KiB  
Article
Enhancement and Compatibilization of Waste-Sourced Biocomposites Through Elastomer Blending and Matrix Grafting Modification
by Shunmin Yi, Wanyu Liu, Shihua Xu, Ruijia Hu, Qing Li, Meijia Wu, Qingwen Wang and Zhimin Huang
Molecules 2024, 29(20), 4905; https://doi.org/10.3390/molecules29204905 - 16 Oct 2024
Viewed by 194
Abstract
A novel elastomer-modified multicomponent, multiphase waste-sourced biocomposites, was prepared for converting waste biomass and plastic into value-added products. The effects of blending elastomer–olefin block copolymer (OBC) and maleic anhydride (MAH), and divinylbenzene (DVB) co-grafting of recycled polypropylene (rPP) matrix on the adhesion interface, [...] Read more.
A novel elastomer-modified multicomponent, multiphase waste-sourced biocomposites, was prepared for converting waste biomass and plastic into value-added products. The effects of blending elastomer–olefin block copolymer (OBC) and maleic anhydride (MAH), and divinylbenzene (DVB) co-grafting of recycled polypropylene (rPP) matrix on the adhesion interface, structure, and properties of high wood flour-filled (60 wt.%) composites were thoroughly investigated. The results indicated that DVB introduced branched structures into the polymer matrix molecular chain and increased the MAH grafting rate. Co-grafting rPP/OBC blends enhanced the interfacial adhesion among rPP, OBC, and wood flour. Additionally, MAH-grafted OBC was prone to encapsulating rigid wood flour, thereby forming an embedded structure. Notably, the tensile modulus and impact strength of the final three-component composites increased by 60% and 125%, respectively, compared with the unmodified composites. Additionally, dynamic mechanical analysis revealed that DVB-induced branching promoted the formation of microvoids in the OBC shell layer surrounding the wood, which in turn induced significant plastic deformation in the polymer matrix. This work offers a facile and efficient method for preparing high-toughness, high-stiffness, and low-cost waste PP-based composites for automotive interiors, and indoor and outdoor decoration. Full article
(This article belongs to the Special Issue π-Conjugated Functional Molecules & Polymers)
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<p>FTIR spectra (<b>a</b>,<b>b</b>), MAH grafting degree (<b>c</b>), and melt flow rate (<b>d</b>) of the modified rPP.</p>
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<p>Rheological behavior of polymer matrix: (<b>a</b>) storage modulus; (<b>b</b>) loss damping; (<b>c</b>) complex viscosity; (<b>d</b>) loss viscosity–storage viscosity curves.</p>
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<p>Fracture morphology of polymer matrix: (<b>a</b>) rPP; (<b>b</b>) rPM; (<b>c</b>) rPMD; (<b>d</b>) rPOM; (<b>e</b>) rPOMD.</p>
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<p>DSC curves of the polymer matrix: (<b>a</b>) melting; (<b>b</b>) crystallization.</p>
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<p>Mechanical properties of polymer matrix: (<b>a</b>) tensile stress–strain curves; (<b>b</b>) impact strength; (<b>c</b>) tensile strength; (<b>d</b>) tensile modulus.</p>
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<p>Fracture morphology of the composites: (<b>a</b>,<b>b</b>) WrP; (<b>c</b>,<b>d</b>) WrPM; (<b>e</b>,<b>f</b>) WrPOM; (<b>g</b>,<b>h</b>) WrPOMD.</p>
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<p>Mechanical properties of the composites: (<b>a</b>) tensile strength and modulus; (<b>b</b>) flexural strength and modulus; (<b>c</b>) impact strength.</p>
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<p>(<b>a</b>) Storage modulus, (<b>b</b>) loss modulus, and (<b>c</b>) loss factor of the composites.</p>
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24 pages, 3355 KiB  
Review
Hybrid Fiber-Reinforced Biocomposites for Marine Applications: A Review
by Yang Huang, Mohamed Thariq Hameed Sultan, Farah Syazwani Shahar, Rafał Grzejda and Andrzej Łukaszewicz
J. Compos. Sci. 2024, 8(10), 430; https://doi.org/10.3390/jcs8100430 (registering DOI) - 16 Oct 2024
Viewed by 317
Abstract
Highly efficient fiber-reinforced composites find extensive application in diverse industries. Yet, conventional fiber-reinforced composites have significant environmental impacts during both manufacturing and disposal. Environmentally friendly fiber-reinforced composites have garnered significant attention within the framework of sustainable development. Utilizing natural fibers in place of [...] Read more.
Highly efficient fiber-reinforced composites find extensive application in diverse industries. Yet, conventional fiber-reinforced composites have significant environmental impacts during both manufacturing and disposal. Environmentally friendly fiber-reinforced composites have garnered significant attention within the framework of sustainable development. Utilizing natural fibers in place of synthetic fibers and progressively decreasing the use of synthetic fibers are the main approaches to achieving a balance between economic progress and environmental quality. Attention is increasingly being drawn to natural fiber-reinforced biocomposites that exhibit outstanding environmental performance, exceptional physical and mechanical capabilities, and biological features. The lightweight and high-strength characteristics of these biocomposites enable them to significantly decrease the weight of structures, making them increasingly popular in many industries. The objective of this review is to evaluate the effectiveness of hybrid fiber-reinforced biocomposites in marine applications, specifically examining their mechanical characteristics, resistance to seawater, and ability to absorb moisture, all while advocating for sustainable material methodologies. To achieve this objective, the paper delineates the distinction between synthetic and natural fibers, examines the benefits of hybrid fiber-reinforced biocomposite materials, and addresses the obstacles and effective approaches in their production and application in seawater. Considering the review analysis, it can be inferred that the use of fiber-reinforced biocomposites in maritime applications shows significant potential and has abundant untapped growth prospects in the future years. Full article
(This article belongs to the Special Issue Recent Progress in Hybrid Composites)
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<p>Development of composite materials.</p>
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<p>Classification of synthetic fibers based on organic, inorganic, and other fibers.</p>
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<p>Structural composition of the cellulose fiber.</p>
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<p>Tensile strength and fracture strain of E-glass fiber (G) and jute fiber (J) hybrid composite laminates.</p>
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<p>Tensile strength, flexural strength and modulus of E-glass fiber (G) and jute fiber (J) composite laminates.</p>
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<p>Hybrid natural fiber-reinforced composites uptake water test: (<b>a</b>) Stacking sequence and nomenclature of biocomposite laminate; (<b>b</b>) Moisture absorption rate after immersion in water at indoor temperature (Reproduced with permission from [<a href="#B73-jcs-08-00430" class="html-bibr">73</a>], Elsevier, 2023).</p>
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<p>The influence of water in the interface between fiber and matrix: (<b>a</b>) Initial state before water absorption; (<b>b</b>) Moisture absorption process; (<b>c</b>) Saturation state; (<b>d</b>) Drying process; (<b>e</b>) Dry state after moisture absorption.</p>
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<p>Mechanical properties of Flax/Epoxy and Hemp/Epoxy: (<b>a</b>) Strength changes under wet and dry conditions; (<b>b</b>) Modulus changes under wet and dry conditions.</p>
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<p>The application of FRPs in marine fields.</p>
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15 pages, 5232 KiB  
Article
Effects of Grapevine Fiber and Additives on the Properties of Polylactic Acid Green Bio-Composites
by Chun-Wei Chang, Chien-Chung Huang, Yi-Jing Jiang, Po-Hsiang Wang and Yeng-Fong Shih
J. Compos. Sci. 2024, 8(10), 422; https://doi.org/10.3390/jcs8100422 - 13 Oct 2024
Viewed by 546
Abstract
In recent years, numerous researchers have incorporated plant fibers into polymers to alter the thermal and mechanical properties of materials. Grapevines, considered agricultural waste, have led to burdens for farmers and environmental challenges due to their mass production. This study aims to reduce [...] Read more.
In recent years, numerous researchers have incorporated plant fibers into polymers to alter the thermal and mechanical properties of materials. Grapevines, considered agricultural waste, have led to burdens for farmers and environmental challenges due to their mass production. This study aims to reduce the brittleness of polylactic acid (PLA) by adding polybutylene succinate (PBS) as a toughening agent and employing grapevine fiber (GVF) as a biomass filler. Additionally, the influence of GVF, toughening agents, compatibilizers, and lubrication agents on the tensile strength, heat deflection temperature (HDT), and impact strength of the composites was examined. The findings revealed that the addition of 10% GVF and 5% PBS increased the impact and tensile strengths of PLA from 17.47 J/m and 49.74 MPa to 29.7 J/m and 54.46 MPa, respectively. Moreover, the HDT of the composites exceeded 120 °C when the GVF content was more than 40 wt%. Additionally, the inclusion of a compatibilizer and a lubrication agent enabled the composite containing 30% GVF to achieve tensile and impact strengths of 45.30 MPa and 25.52 J/m, respectively. Consequently, these GVF/PLA green bio-composites not only improve the mechanical and thermal properties of PLA but also promote the reuse of waste grapevines. Full article
(This article belongs to the Special Issue Sustainable Biocomposites, Volume II)
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<p>(<b>a</b>) Photographs of grapevines and (<b>b</b>) crushed and sieved grapevine powder.</p>
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<p>Preparation of MAH-grafted PBS.</p>
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<p>Preparation of MAH-grafted PLA.</p>
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<p>Preparation of GVF/PLA composites.</p>
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<p>Mechanical and thermal properties of GVF/PLA composites with different content of PBS.</p>
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<p>Mechanical and thermal properties of GVF/PLA composites with different content of GVF.</p>
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<p>Mechanical and thermal properties of GVF/PLA composites modified with PBS-MA.</p>
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<p>Mechanical and thermal properties of GVF/PLA composites modified with PLA-MA.</p>
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<p>Interactions between PLA, PLA-MA, and GVF.</p>
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<p>Mechanical and thermal properties of GVF/PLA composites modified with PLA-MA and lubrication agent.</p>
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<p>SEM images of PLA and its composites: (<b>a</b>) PLA, (<b>b</b>) GP-10-PBS-5, (<b>c</b>) GP-30-PBS-5, (<b>d</b>) GP-40-PBS-5, (<b>e</b>) GP-40-PBS-3, (<b>f</b>) GP-30-PBS-5-PBS-MA-3, (<b>g</b>) MPG-30-5, (<b>h</b>) AMPG-30-5.</p>
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<p>SEM images of PLA and its composites: (<b>a</b>) PLA, (<b>b</b>) GP-10-PBS-5, (<b>c</b>) GP-30-PBS-5, (<b>d</b>) GP-40-PBS-5, (<b>e</b>) GP-40-PBS-3, (<b>f</b>) GP-30-PBS-5-PBS-MA-3, (<b>g</b>) MPG-30-5, (<b>h</b>) AMPG-30-5.</p>
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32 pages, 26302 KiB  
Article
Development of Novel Biocomposites with Antimicrobial-Activity-Based Magnesium-Doped Hydroxyapatite with Amoxicillin
by Carmen Cimpeanu, Daniela Predoi, Carmen Steluta Ciobanu, Simona Liliana Iconaru, Krzysztof Rokosz, Mihai Valentin Predoi, Steinar Raaen and Monica Luminita Badea
Antibiotics 2024, 13(10), 963; https://doi.org/10.3390/antibiotics13100963 - 12 Oct 2024
Viewed by 729
Abstract
Background/Objectives: A biocomposite based on magnesium-doped hydroxyapatite and enriched with amoxicillin (MgHApOx) was synthesized using the coprecipitation method and is presented here for the first time. Methods: The stability of MgHAp and MgHApOx suspensions was evaluated by ultrasound measurements. The structure [...] Read more.
Background/Objectives: A biocomposite based on magnesium-doped hydroxyapatite and enriched with amoxicillin (MgHApOx) was synthesized using the coprecipitation method and is presented here for the first time. Methods: The stability of MgHAp and MgHApOx suspensions was evaluated by ultrasound measurements. The structure of the synthesized MgHAp and MgHApOx was examined with X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The crystalline structure was determined by X-ray diffraction. The FTIR data were collected in the range of 4000–400 cm−1. The morphology of the nanoparticles was evaluated by scanning electron microscopy (SEM). Furthermore, the biocompatible properties of MgHAp, MgHApOx and amoxicillin (Ox) suspensions were assessed using human fetal osteoblastic cells (hFOB 1.19 cell line). The antimicrobial properties of the MgHAp, MgHApOx and Ox suspension nanoparticles were assessed using the standard reference microbial strains Staphylococcus aureus ATCC 25923, Escherichia coli ATCC 25922 and Candida albicans ATCC 10231. Results: X-ray studies have shown that the biocomposite retains the characteristics of HAp and amoxicillin. The SEM assessment exhibited that the apatite contains particles at nanometric scale with acicular flakes morphology. The XRD and SEM results exhibited crystalline nanoparticles. The average crystallite size calculated from XRD analysis increased from 15.31 nm for MgHAp to 17.79 nm in the case of the MgHApOx sample. The energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) analysis highlighted the presence of the constituent elements of MgHAp and amoxicillin. Moreover, XPS confirmed the substitution of Ca2+ ions with Mg2+ and the presence of amoxicillin constituents in the MgHAp lattice. The results of the in vitro antimicrobial assay demonstrated that MgHAp, MgHApOx and Ox suspensions exhibited good antimicrobial activity against the tested microbial strains. The results showed that the antimicrobial activity of the samples was influenced by the presence of the antibiotic and also by the incubation time. Conclusions: The findings from the biological assays indicate that MgHAp and MgHApOx are promising candidates for the development of new biocompatible and antimicrobial agents for biomedical applications. Full article
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<p>Time evolution of the recorded signals of MgHAp suspension from left to right over 5000 s (<b>a</b>); Recorded signals amplitudes during the experiment for MgHAp suspension (<b>b</b>).</p>
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<p>Time evolution of the recorded signals of MgHApOx suspension from left to right over 4500 s (<b>a</b>); Recorded signals amplitudes during the experiment for MgHApOx suspension (<b>b</b>).</p>
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<p>Spectral amplitudes of all recorded signals (<b>a</b>), time-averaged attenuation for the investigated frequency range (<b>b</b>) and relative spectral amplitudes vs. time (<b>c</b>) of MgHAp sample.</p>
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<p>Spectral amplitudes of all recorded signals (<b>a</b>), time-averaged attenuation for the investigated frequency range (<b>b</b>) and relative spectral amplitudes vs. time (<b>c</b>) of MgHApOx sample.</p>
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<p>XRD patterns of MgHAp (<b>b</b>), MgHApOx (<b>c</b>) and Ox (<b>d</b>) samples. The JCPDS # 09-0432 of HAp (<b>a</b>) and JCPDS # 39-1832 of Ox (<b>e</b>). The * indicates the maxima associated with amoxicillin structure.</p>
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<p>XRD patterns of MgHAp (<b>a</b>), MgHApOx (<b>b</b>) relative shift on 2θ range of 25–35°. The * indicates the maxima associated with amoxicillin structure.</p>
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<p>(<b>a</b>,<b>b</b>) SEM micrographs obtained at ×100,000 and at ×200,000 for MgHAp sample; (<b>d</b>,<b>e</b>) SEM micrographs obtained at ×100,000 and at ×200,000 for MgHApOx sample. (<b>c</b>,<b>f</b>) particle size distribution obtained for MgHAp and MgHApOx.</p>
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<p>Energy-dispersive X-ray spectroscopy spectra of (<b>a</b>) MgHAp and (<b>b</b>) MgHApOx.</p>
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<p>FTIR general spectra of MgHAp, MgHApOx and Ox.</p>
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<p>FTIR spectra of MgHAp, MgHApOx and Ox obtained between 900 and 1200 cm<sup>−1</sup> and their second derivative curve.</p>
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<p>Deconvoluted FTIR spectra of the MgHAp, Ox and MgHApOx obtained in the 900–1200 cm<sup>−1</sup> spectral domain.</p>
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<p>General XPS spectra of MgHAp (<b>a</b>) and MgHApOx (<b>b</b>) samples.</p>
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<p>High-resolution XPS spectra and curve-fitting results of C 1s for MgHAp (<b>a</b>) and MgHApOx (<b>b</b>); O1s for MgHAp (<b>c</b>) and MgHApOx (<b>d</b>); Ca2p for MgHAp (<b>e</b>) and MgHApOx (<b>f</b>); P2p for MgHAp (<b>g</b>) and MgHApOx (<b>h</b>).</p>
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<p>High-resolution XPS spectra and curve-fitting results of Mg 2p for MgHAp (<b>a</b>) and MgHApOx (<b>b</b>).</p>
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<p>High-resolution XPS spectra and curve-fitting results of N1s (<b>a</b>) and S 2p (<b>b</b>) for MgHApOx sample.</p>
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<p>Percentage hemolysis of sheep red blood cells (RBCs) exposed to different concentrations of MgHAp, MgHApOx and Ox suspensions. The statistical analysis of the data was performed using one-way ANOVA. The calculated <span class="html-italic">p</span>-values were <span class="html-italic">p</span> &lt; 0.002.</p>
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<p>MTT assay of hFOB 1.19 cells incubated with MgHAp, MgHApOx and Ox suspensions for 24, 48 and 72 h. The results are represented as mean ± standard deviation (SD) and are expressed as percentages of control (100% viability). The statistical analysis of the data was performed using one-way ANOVA. The <span class="html-italic">p</span>-values indicated are * <span class="html-italic">p</span> ≤ 0.002, ** <span class="html-italic">p</span> ≤ 0.001, *** <span class="html-italic">p</span> ≤ 0.0001.</p>
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<p>Lactate dehydrogenase (LDH) activity released in the culture medium of hFOB 1.19 cells after the treatment with MgHAp, MgHApOx and Ox suspensions for 24, 48 and 72 h. The results are represented as mean ± standard deviation (SD). The statistical analysis of the data was performed using one-way ANOVA. The <span class="html-italic">p</span>-values indicated are * <span class="html-italic">p</span> ≤ 0.002, ** <span class="html-italic">p</span> ≤ 0.001, *** <span class="html-italic">p</span> ≤ 0.0001.</p>
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<p>Graphical representation of the logarithmic values of colony forming units (CFU)/mL of <span class="html-italic">S. aureus</span> ATCC 25923 (<b>a</b>), <span class="html-italic">E. coli</span> ATCC 25922 (<b>b</b>) and <span class="html-italic">C. albicans</span> ATCC 10231 (<b>c</b>) microbial strains after 24, 48 and 72 h of exposure to MgHAp, MgHApOx and Ox suspensions. #—depicts the bactericidal properties of the samples. The results are represented as mean ± standard error. Ordinary one-way ANOVA was used for the statistical analysis. The <span class="html-italic">p</span>-values indicated are * <span class="html-italic">p</span> ≤ 0.002, ** <span class="html-italic">p</span> ≤ 0.001, *** <span class="html-italic">p</span> ≤ 0.0001.</p>
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<p>The schematic representation (<b>a</b>) and the image (<b>b</b>) of US experimental setup [<a href="#B95-antibiotics-13-00963" class="html-bibr">95</a>].</p>
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14 pages, 8297 KiB  
Article
The Role of Methods for Applying Cucurbit[6]uril to Hydroxyapatite for the Morphological Tuning of Its Surface in the Process of Obtaining Composite Materials
by Tolkynay Burkhanbayeva, Arthur Ukhov, Dina Assylbekova, Zukhra Mussina, Irina Kurzina, Sandugash Abilkasova, Abdigali Bakibaev, Manar Issabayeva, Rakhmetulla Yerkassov and Zhanat Shaikhova
Materials 2024, 17(20), 4995; https://doi.org/10.3390/ma17204995 - 12 Oct 2024
Viewed by 287
Abstract
In this work, composite materials were obtained for the first time using various methods and the dependences of the resulting surface morphologies were investigated. This involves modifying the surface with cucurbit[n]urils, which are highly promising macrocyclic compounds. The process includes applying cucurbit[6]uril to [...] Read more.
In this work, composite materials were obtained for the first time using various methods and the dependences of the resulting surface morphologies were investigated. This involves modifying the surface with cucurbit[n]urils, which are highly promising macrocyclic compounds. The process includes applying cucurbit[6]uril to the hydroxyapatite surface in water using different modification techniques. The first method involved precipitating a dispersion of CB[6] in undissolved form in water. The second method involved using fully dissolved CB[6] in deionized water, after which the composite materials were dried to constant weight. The third method involved several steps: first, CB[6] was dissolved in deionized water, then, upon heating, a dispersion of CB[6] was formed on the surface of HA. The fourth method involved using ultrasonic treatment. All four methods yielded materials with different surface morphologies, which were studied and characterized using techniques such as infrared (IR) spectroscopy and scanning electron microscopy (SEM). Based on these results, it is possible to vary the properties and surface morphology of the obtained materials. Depending on the method of applying CB[6] to the surface and inside the HA scaffold, it is possible to adjust the composition and structure of the target composite materials. The methods for applying CB[6] to the hydroxyapatite surface enhance its versatility and compatibility with the body’s environment, which is crucial for developing new functional composite materials. This includes leveraging supramolecular systems based on the CB[n] family. The obtained results can be used to model the processes of obtaining biocomposite materials, as well as to predict the properties of future materials with biological activity. Full article
(This article belongs to the Section Advanced Nanomaterials and Nanotechnology)
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<p>Diffractogram of synthesized stoichiometric <b>HA</b> (red line—synthesized HA, green line—standard).</p>
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<p>Synthesis scheme <b>CB[6]</b>.</p>
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<p>X-ray diffraction pattern <b>CB[6]</b>.</p>
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<p>Scheme for applying <b>CB[6]</b> to the <b>HA</b> surface.</p>
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<p>IR spectrum of the cleavage composite obtained by <b>Method 1</b>, <b>CB[6]</b> (green line), <b>HA</b> (orange line) and composite (blue line).</p>
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<p>IR spectrum of the cleavage composite obtained by <b>Method 2</b>, <b>CB[6]</b> (green line), <b>HA</b> (orange line) and composite (blue line).</p>
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<p>SEM images of samples obtained by <b>Method 1</b> ((<b>A</b>) 1500× magnification, (<b>B</b>) 3000× magnification).</p>
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<p>SEM images of samples obtained by <b>Method 2</b> ((<b>A</b>) 1500× magnification, (<b>B</b>) 10,000× magnification).</p>
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<p>Schematic representation of the formation of conglomerates of <b>CB[6]</b> molecules on the surface of <b>HA</b> using <b>Method 2</b>.</p>
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<p>SEM images of samples obtained by <b>Method 3</b> ((<b>A</b>) 500× magnification, (<b>B</b>) 4000× magnification).</p>
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<p>Scheme for producing composites using ultrasonic interaction.</p>
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<p>SEM images of composites obtained by <b>Method 3</b> (<b>upper image</b>) and when composites were obtained by ultrasound interaction (<b>lower image</b>)<b>.</b></p>
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15 pages, 6273 KiB  
Article
New Refined Experimental Analysis of Fungal Growth in Degraded Bio-Based Materials
by Dmytro Kosiachevskyi, Kamilia Abahri, Isabelle Trinsoutrot-Gattin, Lisa Castel, Anne Daubresse, Mohend Chaouche and Rachid Bennacer
Processes 2024, 12(10), 2188; https://doi.org/10.3390/pr12102188 - 9 Oct 2024
Viewed by 480
Abstract
When exposed to different building environmental conditions, bio-composite materials, such as hemp mortars, represent a risk of mold proliferation. This later plays a critical role in the biodeterioration of the materials when their physical properties are locally modified by the natural aging process. [...] Read more.
When exposed to different building environmental conditions, bio-composite materials, such as hemp mortars, represent a risk of mold proliferation. This later plays a critical role in the biodeterioration of the materials when their physical properties are locally modified by the natural aging process. The primary objectives of the present work are first to assess the evolution of the surface of contaminated mortar; second, to investigate an accurate DNA extraction method that could be used for both bio-composite mortars and their fiber sources collected in situ; then, to understand the process of the proliferation of mold strains on both hemp shives and hemp mortar; and finally, to compare mold strains present in these phases to show their relationship to mold contamination and their impact on human health. In situ hemp mortar contamination behavior was investigated in the region of Pau (France) two months after hemp mortar application in extreme conditions (high humidity, low temperature, no aeration), which did not match the standard conditions under which hemp mortar must be used. The SEM observations and FTIR and pH analyses highlighted the decrease in pH level and the presence of organic matter on the mortar surface. DNA sequencing results showed that hemp shives were the main source of fungal contamination of hemp mortar. A mold population analysis showed that the most dominant phylum was Ophistokonta, which represented 83.6% in hemp shives and 99.97% in hemp mortar. The Acrostalagmus genus representatives were the most abundant, with 42% in hemp shives and 96% in hemp mortar. The interconnection between the mold strain characteristics (particularly the ability to grow in extreme environments) and the presence of hemp mortar was emphasized. Full article
(This article belongs to the Topic Advances in Sustainable Materials and Products)
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<p>Images of mold proliferation on hemp mortar taken from contaminated areas in January 2018 (<b>A</b>) with the optical microscope (<b>B</b>) and with the electronic microscope (<b>C</b>).</p>
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<p>Oxide analysis of used lime-based binder with hydraulic additions.</p>
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<p>Mass ratios of hemp mortar composition.</p>
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<p>Scheme of the DNA extraction protocol.</p>
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<p>ATR-FTIR spectrum obtained from the contaminated hemp mortar sample.</p>
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<p>W-SEM observations of fungal growth on the contaminated hemp mortar samples.</p>
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<p>Diagram of pH level evolution on the surface and in the middle of the samples before and after the weathering aging cycles.</p>
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<p>Rarefaction analysis of the observed OTUs for the hemp shives, the hemp mortar, and the negative control as a function of an increasing number of sequences.</p>
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<p>Relative abundance levels of each fungal phylum for hemp shives (<b>a</b>) and hemp mortar (<b>b</b>).</p>
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<p>Fungal community analysis in hemp shives (18S rDNA).</p>
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<p>Fungal community analysis in hemp mortar (18S rDNA).</p>
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<p>Venn diagram evaluating the mold contamination of hemp shives, hemp mortar, and both.</p>
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43 pages, 8271 KiB  
Review
Valorization of Eggshell as Renewable Materials for Sustainable Biocomposite Adsorbents—An Overview
by Bolanle M. Babalola and Lee D. Wilson
J. Compos. Sci. 2024, 8(10), 414; https://doi.org/10.3390/jcs8100414 - 8 Oct 2024
Viewed by 568
Abstract
The production and buildup of eggshell waste represents a challenge and an opportunity. The challenge is that uncontrolled disposal of generated eggshell waste relates to a sustainability concern for the environment. The opportunity relates to utilization of this biomass resource via recycling for [...] Read more.
The production and buildup of eggshell waste represents a challenge and an opportunity. The challenge is that uncontrolled disposal of generated eggshell waste relates to a sustainability concern for the environment. The opportunity relates to utilization of this biomass resource via recycling for waste valorization, cleaner production, and development of a circular economy. This review explores the development of eggshell powder (ESP) from eggshell waste and a coverage of various ESP composite sorbents with an emphasis on their potential utility as adsorbent materials for model pollutants in solid–liquid systems. An overview of literature since 2014 outlines the development of eggshell powder (ESP) and ESP composite adsorbents for solid–liquid adsorption processes. The isolation and treatment of ESP in its pristine or modified forms by various thermal or chemical treatments, along with the preparation of ESP biocomposites is described. An overview of the physico-chemical characterization of ESP and its biocomposites include an assessment of the adsorption properties with various model pollutants (cations, anions, and organic dyes). A coverage of equilibrium and kinetic adsorption isotherm models is provided, along with relevant thermodynamic parameters that govern the adsorption process for ESP-based adsorbents. This review reveals that ESP biocomposite adsorbents represent an emerging class of sustainable materials with tailored properties via modular synthetic strategies. This review will serve to encourage the recycling and utilization of eggshell biomass waste and its valorization as potential adsorbent systems. The impact of such ESP biosorbents cover a diverse range of adsorption-based applications from environmental remediation to slow-release fertilizer carrier systems in agricultural production. Full article
(This article belongs to the Special Issue Sustainable Biocomposites, Volume II)
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<p>Global egg production for two decades, where production (10<sup>6</sup> metric tons) covers a four-decade period. Redrawn with permission from [<a href="#B15-jcs-08-00414" class="html-bibr">15</a>].</p>
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<p>The overall structure of an egg and the eggshell. Copied with permission [<a href="#B26-jcs-08-00414" class="html-bibr">26</a>].</p>
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<p>Steps involved in the preparation of ESP.</p>
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<p>General flowchart of the preparatory steps for making eggshell biocomposite materials that contain various additives (1 to 8), as follows: (1) anthill clay, (2) multi-walled carbon nanotubes (MWCNTs), (3) sodium alginate, (4) titanium dioxide, (5) strontium ferrite, (6) eggshell powder (ESP), (7) sodium dodecyl sulfate (SDS), and (8) chitosan/acetic acid.</p>
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<p>Typical characterization results of ESP. (<b>A</b>) SEM: (a) ESP; (b) CES; (<b>B</b>) XRD; (<b>C</b>) XPS; (<b>D</b>) IR copied with permission [<a href="#B7-jcs-08-00414" class="html-bibr">7</a>,<a href="#B58-jcs-08-00414" class="html-bibr">58</a>,<a href="#B59-jcs-08-00414" class="html-bibr">59</a>].</p>
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<p>Simplified illustration of an adsorption experiment. Adapted and redrawn with permission [<a href="#B74-jcs-08-00414" class="html-bibr">74</a>].</p>
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<p>Adsorption of an adsorbate in the liquid phase onto a solid adsorbent at the solid–liquid interface. The circles depict the adsorbate particles while the dashed line represent the imaginary interface boundary. Copied and modified with permission [<a href="#B77-jcs-08-00414" class="html-bibr">77</a>].</p>
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<p>Contributing factors for the adsorption mechanism of pollutants onto eggshell particles. Copied with permission [<a href="#B146-jcs-08-00414" class="html-bibr">146</a>].</p>
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<p>Application of eggshell in various industries. Copied with permission [<a href="#B74-jcs-08-00414" class="html-bibr">74</a>].</p>
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<p>Application of eggshell waste in catalysis.</p>
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<p>Application of ES as a photocatalyst in water treatment. Copied and redrawn with permission [<a href="#B59-jcs-08-00414" class="html-bibr">59</a>].</p>
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<p>Application of eggshell as a slow-release fertilizer system. Adapted with permission [<a href="#B195-jcs-08-00414" class="html-bibr">195</a>].</p>
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<p>(<b>a</b>) Water holding capacity and (<b>b</b>) water retention capacity of soil with and without ES and ES-SRF. Copied and modified with permission [<a href="#B195-jcs-08-00414" class="html-bibr">195</a>].</p>
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<p>The use of granular ternary agro-waste adsorbent for orthophosphate uptake at pH 4.5 and 8.5. Copied with permission [<a href="#B16-jcs-08-00414" class="html-bibr">16</a>].</p>
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<p>Application of eggshell in treatment of water containing metal-ion species. Copied with permission [<a href="#B197-jcs-08-00414" class="html-bibr">197</a>].</p>
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14 pages, 9262 KiB  
Article
Innovative Hemp Shive-Based Bio-Composites: Part I: Modification of Potato Starch Binder by Sodium Meta-Silicate and Glycerol
by Laura Vitola, Ina Pundiene, Jolanta Pranckeviciene and Diana Bajare
Materials 2024, 17(19), 4911; https://doi.org/10.3390/ma17194911 - 8 Oct 2024
Viewed by 421
Abstract
The growing demand for sustainable building materials has boosted research on plant-based composite materials, including hemp shives bound with biodegradable binders. This study investigates the enhancement of potato-starch-based binders with sodium metasilicate and glycerol to produce eco-friendly bio-composites incorporating hemp shives. Potato starch, [...] Read more.
The growing demand for sustainable building materials has boosted research on plant-based composite materials, including hemp shives bound with biodegradable binders. This study investigates the enhancement of potato-starch-based binders with sodium metasilicate and glycerol to produce eco-friendly bio-composites incorporating hemp shives. Potato starch, while renewable, often results in suboptimal mechanical properties and durability in its unmodified form. The addition of sodium metasilicate is known to improve the mechanical strength and thermal stability of starch-based materials, while glycerol acts as a plasticizer, potentially enhancing flexibility and workability. Bio-composites were produced with varying concentrations of sodium metasilicate (0–107% by mass of starch) and glycerol (0–133% by mass of starch), and their properties were evaluated through thermal analysis, density measurements, water absorption tests, compressive strength assessments, and thermal conductivity evaluations. The results demonstrate that sodium metasilicate significantly increases the bulk density, water resistance, and compressive strength of the bio-composites, with enhancements up to 19.3% in density and up to 2.3 times in compressive strength. Glycerol further improves flexibility and workability, though excessive amounts can reduce compressive strength. The combination of sodium metasilicate and glycerol provides optimal performance, achieving the best results with an 80% sodium metasilicate and 33% glycerol mixture by weight of starch. These modified bio-composites offer promising alternatives t2 o conventional building materials with improved mechanical properties and environmental benefits, making them suitable for sustainable construction applications. Full article
(This article belongs to the Section Construction and Building Materials)
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<p>Scheme of binder and bio-composite preparation process.</p>
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<p>Differential scanning calorimetry (DSC) (solid line) and thermogravimetric analysis (TGA) (dotted line) of studied potato starch binders.</p>
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<p>FTIR transmittance spectra of studied potato starch binders.</p>
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<p>Microstructure of obtained potato starch binder.</p>
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<p>The obtained bio-composites bounded by potato starch binder.</p>
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<p>The microstructure of obtained bio-composites bounded by a potato starch binder modified by sodium metasilicate solution and glycerol (BC-120-25).</p>
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<p>The index of the bulk density of obtained bio-composites bounded by potato starch binder modified by sodium metasilicate solution and glycerol.</p>
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<p>The index of the capillary water absorption of obtained bio-composites bounded by potato starch binder modified by sodium metasilicate solution and glycerol. (green background: acceptable results).</p>
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<p>The index of compressive strength of obtained bio-composites bounded by potato starch binder modified by sodium metasilicate solution and glycerol.</p>
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21 pages, 4106 KiB  
Article
An Investigation of the Mechanical Properties of Flax/Basalt Epoxy Hybrid Composites from a Sustainability Perspective
by Martina Panico, Ersilia Cozzolino, Ilaria Papa, Iman Taha and Valentina Lopresto
Polymers 2024, 16(19), 2839; https://doi.org/10.3390/polym16192839 - 8 Oct 2024
Viewed by 575
Abstract
Currently, sustainability plays a central role in the response to global challenges, strongly influencing decisions in various sectors. From this perspective, global efforts to explore inventive and eco-friendly solutions to address the demands of industrialization and large-scale production are being made. Bio-based composites [...] Read more.
Currently, sustainability plays a central role in the response to global challenges, strongly influencing decisions in various sectors. From this perspective, global efforts to explore inventive and eco-friendly solutions to address the demands of industrialization and large-scale production are being made. Bio-based composites needed for lightweight applications benefit from the integration of natural fibers, due to their lower specific weight compared to synthetic fibers, contributing to the overall reduction in the weight of such structures without compromising the mechanical performance. Nevertheless, challenges arise when using natural fibers in composite laminates and hybridization seems to be a solution. However, there is still a lack of knowledge in the literature regarding the strategies and possibilities for reducing laminate thickness, without sacrificing the mechanical performance. This work aims to fill this knowledge gap by investigating the possibility of reducing the laminate thickness in hybrid flax/basalt composites made of plies, organized in the same stacking sequence, through only varying their number. Tensile, Charpy, flexural, and drop-weight tests were carried out for the mechanical characterization of the composites. The results obtained confirm the feasibility of achieving thinner hybrid composites, thus contributing to sustainability, while still having acceptable mechanical properties for structural applications. Full article
(This article belongs to the Special Issue Natural Fiber-Based Green Materials)
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<p>Typical stress–strain trends for the IP<sub>6</sub>, IP<sub>9</sub>, and IP<sub>12</sub> configurations.</p>
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<p>Typical flexural stress–strain trends for the IP<sub>6</sub>, IP<sub>9</sub>, and IP<sub>12</sub> configurations.</p>
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<p>Impact strength and energy absorbed as a function of the number of plies.</p>
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<p>Microscopic detail of Charpy test specimens, labelled as follows: (<b>a</b>) IP<sub>6</sub>; (<b>b</b>) IP<sub>9</sub>; and (<b>c</b>) IP<sub>12</sub>.</p>
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<p>Force vs. displacement penetration and indentation curves for different levels of impact energy: (<b>a</b>) IP<sub>6</sub>; (<b>b</b>) IP<sub>9</sub>; and (<b>c</b>) IP<sub>12</sub>.</p>
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<p>Pictures of IP<sub>6</sub>, IP<sub>9</sub>, and IP<sub>12</sub> specimens impacted by the same level of energy, I<sub>e</sub>, at penetration.</p>
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<p>Pictures of the indentation damage that occurred on the IP<sub>6</sub> specimens, impacted with three different levels of impact energy I<sub>e</sub>.</p>
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<p>Pictures of the indentation damage that occurred on the IP<sub>9</sub> specimens, impacted with three different levels of impact energy I<sub>e</sub>.</p>
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<p>Pictures of the indentation damage that occurred on the IP<sub>12</sub> specimens, impacted with three different levels of impact energy I<sub>e</sub>.</p>
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<p>Example of indentation damage depth measurement (IP<sub>12</sub>, I<sub>e</sub> = 25 J).</p>
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<p>Variation in the indentation damage depth as a function of impact energy for each lamination configuration IP<sub>6</sub>, IP<sub>9</sub>, and IP<sub>12</sub>.</p>
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15 pages, 5717 KiB  
Article
Topical Biocomposites Based on Collagen, Hyaluronic Acid and Metronidazole as Periodontitis Treatment
by Madalina Georgiana Albu Kaya, Alice Geanina Simonca, Ileana Rau, Alina Elena Coman, Minodora Maria Marin, Lacramioara Popa, Roxana Trusca, Cristina-Elena Dinu-Pirvu and Mihaela Violeta Ghica
Pharmaceuticals 2024, 17(10), 1336; https://doi.org/10.3390/ph17101336 - 7 Oct 2024
Viewed by 432
Abstract
Background: It is well known that periodontitis affects the gums and surrounding connective tissue. The chronic inflammatory response induced by bacteria in the gingival tissue leads to the loss of the collagen connection between the tooth and the bone and ultimately to bone [...] Read more.
Background: It is well known that periodontitis affects the gums and surrounding connective tissue. The chronic inflammatory response induced by bacteria in the gingival tissue leads to the loss of the collagen connection between the tooth and the bone and ultimately to bone loss. Methods: In this context, the aim of this research was the obtaining and characterization of a drug release supports in the form of sponges based on collagen, hyaluronic acid as a support and metronidazole as an antibiotic for the treatment of periodontitis. The sponges were characterized by FT-IR spectroscopy, water uptake, contact angle, SEM microscopy, in vitro metronidazole release analysis from sponges and data modeling. Results: The results showed that all the sponges had a porous structure with interconnected pores, the pore sizes being influenced by hyaluronic acid and metronidazole; the spongious structure became much more dense for samples with metronidazole content. All metronidazole-loaded sponges showed good surface wettability and an adequate swelling capacity for a suitable antimicrobial release at the periodontal pocket. The porous structures allow a controlled release, fast in the first hour, essential to control the initial microbial load at the periodontal level, which continues slowly in the following hours to ensure an effective treatment of periodontitis. Conclusions: Correlating all physical–chemical and bio-pharmaceutical results obtained, a promising solution for periodontitis treatment could be a met-ronidazole–collagen–hyaluronic system consisting of 1% collagen, 1.5% metronidazole and 0.8% hyaluronic acid, and in vitro and in vivo tests are recommended to continue studies. Full article
(This article belongs to the Special Issue Development of Specific Dosage Form: Wound Dressing)
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<p>The FT-IR spectra for (<b>a</b>) M1 collagen; (<b>b</b>) HA-HA; (<b>c</b>) MTZ-MTZ; (<b>d</b>) the spongious matrices M1-M6.</p>
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<p>The FT-IR spectra for (<b>a</b>) M1 collagen; (<b>b</b>) HA-HA; (<b>c</b>) MTZ-MTZ; (<b>d</b>) the spongious matrices M1-M6.</p>
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<p>SEM images of M1–M6 sponges: (<b>a</b>) M1 (×500 magnification); (<b>b</b>) M2 (×500 magnification); (<b>c</b>) M3 (×500 magnification); (<b>d</b>) M3 (×2000 magnification); (<b>e</b>) M3 (×5000 magnification); (<b>f</b>) M4 (×500 magnification); (<b>g</b>) M4 (×2000 magnification); (<b>h</b>) M5 (×500 magnification); (<b>i</b>) M6 (×500 magnification).</p>
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<p>SEM images of M1–M6 sponges: (<b>a</b>) M1 (×500 magnification); (<b>b</b>) M2 (×500 magnification); (<b>c</b>) M3 (×500 magnification); (<b>d</b>) M3 (×2000 magnification); (<b>e</b>) M3 (×5000 magnification); (<b>f</b>) M4 (×500 magnification); (<b>g</b>) M4 (×2000 magnification); (<b>h</b>) M5 (×500 magnification); (<b>i</b>) M6 (×500 magnification).</p>
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<p>Water uptake ability of M1–M6 matrices. Results are not statistically significant (ns) for <span class="html-italic">p</span>-value &gt; 0.05; results are statistically significant for <span class="html-italic">p</span>-value as follows: ** <span class="html-italic">p</span>  &lt;  0.01, **** <span class="html-italic">p</span>  &lt;  0.0001.</p>
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<p>Images of the drop shape and the corresponding contact angle mean values for the spongious matrices: (<b>a</b>) M1; (<b>b</b>) M2; (<b>c</b>) M3; (<b>d</b>) M4; (<b>e</b>) M5; (<b>f</b>) M6.</p>
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<p>Plot of % cumulative drug release profiles from the sponges versus time.</p>
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16 pages, 4805 KiB  
Article
Properties of Multiple-Processed Natural Short Fiber Polypropylene and Polylactic Acid Composites: A Comparison
by Barbara Liedl, Thomas Höftberger and Christoph Burgstaller
Macromol 2024, 4(4), 723-738; https://doi.org/10.3390/macromol4040043 - 5 Oct 2024
Viewed by 817
Abstract
Natural fiber composites have gained increasing attention due to sustainability considerations. One often neglected aspect is the potential for the mechanical recycling of such materials. In this work, we compounded injection-molded polypropylene (PP) and polylactic acid (PLA) short cellulose fiber composites with fiber [...] Read more.
Natural fiber composites have gained increasing attention due to sustainability considerations. One often neglected aspect is the potential for the mechanical recycling of such materials. In this work, we compounded injection-molded polypropylene (PP) and polylactic acid (PLA) short cellulose fiber composites with fiber shares up to 40 percent by weight. Both matrix materials were reinforced by the addition of the fibers. We investigated a trifold full recycling process, where we subjected the materials produced in the first place to compounding, injection molding, testing, and shredding, and then repeated the process. Although the materials’ properties assigned to degradation were found to decrease with progressive recycling, attractive mechanical properties could be preserved even after the third reprocessing cycle. Full article
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<p>Process overview for this study: The initial materials were produced by compounding matrix materials with a respective fiber share. The granules were injection-molded to the universal test specimen. A set of these were taken for testing the material properties; the rest of the specimens, the sprues, and the runners were shredded to pieces of less than 5 mm in size and extruded again for a total of three cycles.</p>
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<p>Elastic modulus (<b>a</b>) and tensile strength (<b>b</b>) of PP– and PLA–matrix compounds plotted against the fiber volume share.</p>
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<p>Strain at break (<b>a</b>) and notched Charpy impact strength (<b>b</b>) of PP– and PLA–matrix compounds plotted against the fiber volume share. For a better visualization, the standard deviation at PP with 0 vol% cellulose fiber was omitted; the actual value is 130.4 kJ/m<sup>2</sup>, with a standard deviation of 90.8%.</p>
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<p>Image taken of PP– (<b>left</b>) and PLA–matrix compounds (<b>right</b>), with an intended fiber share of 0, 10, 30, and 40 wt% (from top to bottom) after processing and three reprocessing cycles (from left to right).</p>
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<p>Lightness (L*) of PP– (<b>a</b>) and PLA–cellulose fiber composites (<b>b</b>) with an intended fiber share of 0, 10, 30, and 40 wt%. The pure materials were transparent and were therefore measured on a white standard background.</p>
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<p>E-modulus of PP– (<b>a</b>) and PLA–cellulose fiber composites (<b>b</b>), with an intended fiber share of 0, 10, 30, and 40 wt%.</p>
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<p>Tensile strength of PP– (<b>a</b>) and PLA–cellulose fiber composites (<b>b</b>), with an intended fiber share of 0, 10, 30, and 40 wt%.</p>
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<p>Strain at break of PP– (<b>a</b>) and PLA–cellulose fiber composites (<b>b</b>), with an intended fiber share of 0, 10, 30, and 40 wt%.</p>
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<p>Notched Charpy impact strength of PP- (<b>a</b>) and PLA-cellulose fiber composites (<b>b</b>), with an intended fiber share of 0, 10, 30, and 40 wt%.</p>
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<p>Melt volume flow rate (MVR) of PP– (<b>a</b>) and PLA–cellulose fiber composites (<b>b</b>), with an intended fiber share of 0, 10, 30, and 40 wt%.</p>
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<p>Oxidation induction time (OIT) of PP– (<b>a</b>) and intrinsic viscosity (IV) of PLA–cellulose fiber composites (<b>b</b>), with an intended fiber share of 0, 10, 30, and 40 wt%.</p>
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<p>Microscopic images of the extracted fibers from PP containing 40 wt% cellulose after different reprocessing cycles with a magnification of 32×. Scale bar in the upper left picture represents 500 µm and is valid for all pictures.</p>
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<p>SEM images of the surface fractures of the cryo-broken test specimen of PP (<b>top</b>) and PLA (<b>bottom</b>), with 10 wt% cellulose fibers after different reprocessing cycles. Scale bar in the lower left picture represents 100 µm, and is valid for all pictures.</p>
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<p>IFSS calculated from modified Kelly–Tyson equation (Equation (2)) for PP and PLA compounds, with an assumed fiber length of 500 µm.</p>
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<p>Normalized fiber length degradation, calculated from modified Kelly–Tyson equation (Equation (2)) for PP (<b>a</b>) and PLA (<b>b</b>) compounds reprocessed three times, assuming that τ<sub>c</sub> is constant.</p>
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37 pages, 4470 KiB  
Review
A Review of Natural Fibres and Biopolymer Composites: Progress, Limitations, and Enhancement Strategies
by Innes McKay, Johnattan Vargas, Liu Yang and Reda M. Felfel
Materials 2024, 17(19), 4878; https://doi.org/10.3390/ma17194878 - 4 Oct 2024
Viewed by 941
Abstract
The interest in natural fibres and biopolymers for developing bio-composites has greatly increased in recent years, motivated by the need to reduce the environmental impact of traditional synthetic, fossil fuel-derived materials. However, several limitations associated with the use of natural fibres and polymers [...] Read more.
The interest in natural fibres and biopolymers for developing bio-composites has greatly increased in recent years, motivated by the need to reduce the environmental impact of traditional synthetic, fossil fuel-derived materials. However, several limitations associated with the use of natural fibres and polymers should be addressed if they are to be seriously considered mainstream fibre reinforcements. These include poor compatibility of natural fibres with polymer matrices, variability, high moisture absorption, and flammability. Various surface treatments have been studied to tackle these drawbacks, such as alkalisation, silane treatment, acetylation, plasma treatment, and polydopamine coating. This review paper considers the classification, properties, and limitations of natural fibres and biopolymers in the context of bio-composite materials. An overview of recent advancements and enhancement strategies to overcome such limitations will also be discussed, with a focus on mechanical performance, moisture absorption behaviour, and flammability of composites. The limitations of natural fibres, biopolymers, and their bio-composites should be carefully addressed to enable the widespread use of bio-composites in various applications, including electronics, automotive, and construction. Full article
(This article belongs to the Section Advanced Composites)
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<p>Classification of common natural fibres by origin.</p>
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<p>Tensile strength vs. diameter of common plant fibres.</p>
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<p>Extracted fibres of flax (<b>a</b>) [<a href="#B40-materials-17-04878" class="html-bibr">40</a>], hemp (<b>b</b>) [<a href="#B41-materials-17-04878" class="html-bibr">41</a>], jute (<b>c</b>) [<a href="#B42-materials-17-04878" class="html-bibr">42</a>], kenaf (<b>d</b>) [<a href="#B42-materials-17-04878" class="html-bibr">42</a>], sisal (<b>e</b>) [<a href="#B42-materials-17-04878" class="html-bibr">42</a>], abaca (<b>f</b>) [<a href="#B42-materials-17-04878" class="html-bibr">42</a>], bamboo (<b>g</b>) [<a href="#B43-materials-17-04878" class="html-bibr">43</a>], bagasse (<b>h</b>) [<a href="#B42-materials-17-04878" class="html-bibr">42</a>], cotton (<b>i</b>) [<a href="#B42-materials-17-04878" class="html-bibr">42</a>], coir (<b>j</b>) [<a href="#B32-materials-17-04878" class="html-bibr">32</a>], asbestos (<b>k</b>) [<a href="#B44-materials-17-04878" class="html-bibr">44</a>], and regenerated cellulose fibres (<b>l</b>) [<a href="#B45-materials-17-04878" class="html-bibr">45</a>].</p>
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<p>Hierarchical structure of flax fibre, from bast stems to elementary fibres [<a href="#B5-materials-17-04878" class="html-bibr">5</a>].</p>
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<p>Average tensile properties of flax fibre from the literature [<a href="#B5-materials-17-04878" class="html-bibr">5</a>,<a href="#B47-materials-17-04878" class="html-bibr">47</a>,<a href="#B52-materials-17-04878" class="html-bibr">52</a>,<a href="#B53-materials-17-04878" class="html-bibr">53</a>,<a href="#B54-materials-17-04878" class="html-bibr">54</a>,<a href="#B55-materials-17-04878" class="html-bibr">55</a>,<a href="#B56-materials-17-04878" class="html-bibr">56</a>].</p>
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<p>Global plastic production in 2021 by polymer type and origin [<a href="#B71-materials-17-04878" class="html-bibr">71</a>].</p>
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<p>Classification of common biodegradable polymers by origin.</p>
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<p>Chemical structure of (<b>a</b>) PLA, (<b>b</b>) PGA, and (<b>c</b>) PCL [<a href="#B82-materials-17-04878" class="html-bibr">82</a>].</p>
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<p>Chemical structures of (<b>a</b>) PHB [<a href="#B85-materials-17-04878" class="html-bibr">85</a>] and (<b>b</b>) P4HB [<a href="#B86-materials-17-04878" class="html-bibr">86</a>].</p>
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<p>Chemical structure of epoxidised linolein, a major constituent of ESO [<a href="#B99-materials-17-04878" class="html-bibr">99</a>].</p>
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<p>Chemical structure of (<b>a</b>) BOF and (<b>b</b>) DGEI [<a href="#B99-materials-17-04878" class="html-bibr">99</a>].</p>
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<p>Chemical and physical modification of natural fibres [<a href="#B173-materials-17-04878" class="html-bibr">173</a>].</p>
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17 pages, 2693 KiB  
Article
Melt-Processed Polybutylene-Succinate Biocomposites with Chitosan: Development and Characterization of Rheological, Thermal, Mechanical and Antimicrobial Properties
by Remo Merijs-Meri, Janis Zicans, Tatjana Ivanova, Linda Mezule, Aleksandrs Ivanickins, Ivan Bockovs, Juris Bitenieks, Rita Berzina and Alina Lebedeva
Polymers 2024, 16(19), 2808; https://doi.org/10.3390/polym16192808 - 3 Oct 2024
Viewed by 591
Abstract
The current research is devoted to the development and characterization of green antimicrobial polymer biocomposites for food packaging applications. The biocomposites were developed by melt compounding on the basis of two different succinate polymer matrices with varying chain stiffness—polybutylene succinate (PBS) or its [...] Read more.
The current research is devoted to the development and characterization of green antimicrobial polymer biocomposites for food packaging applications. The biocomposites were developed by melt compounding on the basis of two different succinate polymer matrices with varying chain stiffness—polybutylene succinate (PBS) or its copolymer with 20 mol.% of polybutylene adipate (PBSA). Fungi chitosan oligosaccharide (C98) and crustacean chitosan (C95) were used as antimicrobial additives. The rheological properties of the developed biocomposites were determined to clear out the most suitable temperature for melt processing. In addition, mechanical, thermal, barrier and antimicrobial properties of the developed biocomposites were determined. The results of the investigation revealed that PBSA composites with 7 wt% and 10 wt% of the C98 additive were more suitable for the development of green packaging films because of their higher ultimate elongation values, better damping properties as well as their superior anti-microbial behavior. However, due to the lower thermal stability of the C98 additive as well as PBSA, the melt processing temperatures of the composites desirably should not exceed 120 °C. Additionally, by considering decreased moisture vapor barrier properties, it is recommended to perform further modifications of the PBSA-C98 composites through an addition of a nanoclay additive due to its excellent barrier properties and thermal stability. Full article
(This article belongs to the Special Issue Advances in Polymer Composites II)
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Figure 1

Figure 1
<p>Dynamic viscosity <span class="html-italic">η</span> of PBSA (<b>a</b>) and PBS (<b>b</b>) composites with C98 and C95 chitosan additives as a function of frequency v at 100 °C, 120 °C, 140 °C and 160 °C.</p>
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<p>Shear viscosity of PBSA (<b>a</b>) and PBS (<b>b</b>) composites with C98 and C95 chitosan additives as a function of shear rate at 100 °C, 120 °C, 140 °C and 160 °C.</p>
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<p>Tensile modulus <span class="html-italic">E<sub>t</sub></span> (<b>a</b>), yield strength <span class="html-italic">σ<sub>Y</sub></span> (<b>b</b>), strain at yield <span class="html-italic">ε<sub>Y</sub></span> (<b>c</b>), ultimate strength <span class="html-italic">σ<sub>B</sub></span> (<b>d</b>) and strain at break <span class="html-italic">ε<sub>B</sub></span> (<b>e</b>) of PBS and PBSA composites with C98 and C95 chitosan additives as a function of the filler content.</p>
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<p>Tensile modulus <span class="html-italic">E<sub>t</sub></span> (<b>a</b>), yield strength <span class="html-italic">σ<sub>Y</sub></span> (<b>b</b>), strain at yield <span class="html-italic">ε<sub>Y</sub></span> (<b>c</b>), ultimate strength <span class="html-italic">σ<sub>B</sub></span> (<b>d</b>) and strain at break <span class="html-italic">ε<sub>B</sub></span> (<b>e</b>) of PBS and PBSA composites with C98 and C95 chitosan additives as a function of the filler content.</p>
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<p>Storage modulus <span class="html-italic">E’</span> (<b>a</b>) and loss tangent <span class="html-italic">tanδ</span> (<b>b</b>) of PBS and PBSA composites with C98 and C95 chitosan additives as a function of temperature. −40.</p>
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<p>Storage modulus <span class="html-italic">E’</span> (<b>a</b>) and loss tangent <span class="html-italic">tanδ</span> (<b>b</b>) of PBS and PBSA composites with C98 and C95 chitosan additives as a function of temperature. −40.</p>
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<p>Thermogravimetric curves of neat PBS and PBSA matrices, as well as C95 and C98 chitosan additives.</p>
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<p>Thermogravimetric curves of PBSA (<b>a</b>) and PBS (<b>b</b>) composites with C95 and C98 chitosan additives as a function of temperature.</p>
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<p>FTIR spectra of PBSA and PBS composites with C95 and C98 chitosan additives at carboxyl (<b>a</b>) and hydroxyl (<b>b</b>) absorption ranges.</p>
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<p>Antimicrobial efficacy of the developed composites on <span class="html-italic">E. coli</span> (<b>a</b>) and <span class="html-italic">S. cerevisiae</span> (<b>b</b>) cells in surface tests and low soiling conditions. The results are expressed as log CFU per ml. Each point represents at least 3 experimental repeats.</p>
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<p>Moisture vapor sorption kinetic curves and diffusion coefficient <span class="html-italic">D</span> values of PBSA and PBS composites with C95 and C98 chitosan additives.</p>
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15 pages, 4103 KiB  
Case Report
The Management of Wound Healing in Infections after Hip Arthoplasty Using Stimulan and Negative Pressure Wound Therapy
by Florentin Dimofte, Cristina Dimofte, Sorin Ungurianu, Cristina Serban, George Țocu, Nicoleta Cârneciu, Iulia Filip, Laura Bezman, Ana Fulga, Dana Tutunaru, Irina Mihaela Abdulan, Bogdan Mihnea Ciuntu, Raul Mihailov, Alin Mihai Vasilescu and Dorel Firescu
Diagnostics 2024, 14(19), 2206; https://doi.org/10.3390/diagnostics14192206 - 3 Oct 2024
Viewed by 764
Abstract
Background: medical teams continue to face challenges with infections following hip replacement surgery, whether they occur shortly after the procedure or months or years later. Certain medical conditions like diabetes, rheumatoid arthritis, and obesity are risk factors that make patients more susceptible to [...] Read more.
Background: medical teams continue to face challenges with infections following hip replacement surgery, whether they occur shortly after the procedure or months or years later. Certain medical conditions like diabetes, rheumatoid arthritis, and obesity are risk factors that make patients more susceptible to infections. Traditional intervention methods such as DAIR, one-step, or two-step procedures are being enhanced and refined to ensure quicker and more effective treatment. Some cases present particularly difficult challenges, featuring persistent fistulas and unpredictable responses to treatment. Methods: in our article, we share two unique cases, detailing their histories, progressions, and treatment decisions. We explore the use of antibiotic-impregnated calcium biocomposite as a local adjuvant therapy and the application of negative pressure therapy to expedite healing. The system of NWPT has seen widespread uptake and is now implemented routinely for open wounds, such as open fractures, fasciotomies, ulcers, and infected wounds. Results: our findings demonstrate that surgical debridement and calcium sulfate bead insertion successfully treat bone and joint infections without causing any side effects or complications. As a particularity, in the first case, we encountered the exteriorization of Stimulan pearls after surgery, without other complications related to the biocomposite. Conclusions: we have found that NPWT is a beneficial tool in managing complex wounds in both acute and chronic stages, after the infection is cured, reducing the need for frequent dressing changes, shortening hospital stays, and enhancing patient comfort. Full article
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Figure 1
<p>Aspect of the wound upon admission—tegumentary defect in the middle one-third of the scar with an intermittent fistula aspect and modified periregional tissue.</p>
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<p>Intraoperative aspect—exposure of the left hip joint with debridement of the affected tissues.</p>
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<p>Fragments of removed tissue–modified appearance of consistency and color (metallosis).</p>
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<p>Pelvis X-ray with both joints—left total hip arthroplasty with augmented total non-cemented prosthesis with screws in the acetabulum—preoperative aspect.</p>
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<p>X-ray of the left pelvis—highlighting of Stimulan pearls around the prosthesis chamber and in the layer adjacent to the skin.</p>
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<p>Ten days postoperative—wound dehiscence is observed at the scar site in the lower third, with about a quarter of the added pearls being externalized.</p>
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<p>The local appearance of the wound after removal of all externalized pearls and daily grooming of the wound (red granulating wound margins).</p>
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<p>Local aspect after removing the negative pressure kit—granulation can be seen both deep in the wound and around the edges.</p>
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<p>Appearance after final suture of the wound.</p>
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<p>Final aspect—healed scar.</p>
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<p>Keloid scar—in the lower third of the post-operative scar (knee region), a sub-tegumentary collection can be seen bulging the skin.</p>
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<p>Collection starting to externalize—seropurulent secretion with wheals (about 45 mL modified content).</p>
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<p>Sequence of images from the preparation of Stimulan pearls. (<b>a</b>) Mixing the biocomposite powder with Vancomycin and Gentamicin powders and blending with the liquid content until a paste is formed. (<b>b</b>) Adding the mixed paste into the silicone mold to form the pearls. (<b>c</b>) Final appearance of Stimulan pearls—different sizes. (<b>d</b>) Application of Stimulan pearls at the site of infection.</p>
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<p>Control X-ray of the prosthesis and biocomposite—in the knee region the position of the Stimulan pearls on the side.</p>
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<p>Day 5 postintervention—infiltrated dressing with serous content (about 80 mL).</p>
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<p>Day 5 postintervention—on the dressing, there was a yellowish seromucculent secretion and, from the wound, a continuous, serosanguininolent secretion.</p>
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<p>Day 10 postintervention—the same secretion but reduced in quantity, otherwise clean wound appearance.</p>
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<p>Local aspect 4 weeks after intervention—most of the sutures were removed, except in the area where the secretion was present; those sutures were subsequently removed. The local appearance is inflammatory, slightly red, with no signs of cicatrization.</p>
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<p>Two weeks after placing the negative pressure kit—in the area of the defect, the black sponge applied in the integumentary defect can be seen. No inflammatory signs or secondary secretion.</p>
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<p>Two weeks after removing the negative pressure kit—the consistent narrowing of the skin defect. Thigh and knee were smooth without inflammatory manifestations and without secondary secretion.</p>
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