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Search Results (9,266)

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Keywords = nanocomposite

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18 pages, 9848 KiB  
Article
Degradation of Methyl Orange from Aqueous Solution Using Fe-Ni-Co-Based Trimetallic Nanocomposites: Optimization by Response Surface Methodology
by Areeba Riaz, Bibi Saba Ibrar, Khansa Bibi, Zunaira Habib, Sadaf Ikram, Hafiz Muhammad Aamir Shahzad, Pin Zhao and Zahra Zahra
Sustainability 2024, 16(16), 6958; https://doi.org/10.3390/su16166958 - 14 Aug 2024
Abstract
Effluent-containing dye molecules is a significant environmental hazard. An economical and energy-saving solution is needed to combat this issue for the purpose of environmental sustainability. In this study, Fe-Ni-Co-based trimetallic nanocomposite was synthesized using the coprecipitation method. Scanning Electron Microscopy (SEM), X-ray diffraction [...] Read more.
Effluent-containing dye molecules is a significant environmental hazard. An economical and energy-saving solution is needed to combat this issue for the purpose of environmental sustainability. In this study, Fe-Ni-Co-based trimetallic nanocomposite was synthesized using the coprecipitation method. Scanning Electron Microscopy (SEM), X-ray diffraction (XRD), and Fourier Transform Infra-Red spectroscopy were conducted to explore the physical morphology, phase structure and functional groups of the synthesized catalyst. Among dyes, methyl orange is considered as a major contaminant in textile effluent. The current study focused on the degradation of methyl orange using a trimetallic Fe-Ni-Co-based nanocomposite. A central composite design in response surface methodology was employed to analyze the independent variables including dye concentration, catalyst dose, temperature, hydrogen peroxide, irradiation time, and pH. Dye degradation has been achieved up to 81% in 20 min at the lowest initial concentration (5 mg/L) in optimized conditions. Based on ANOVA, the predicted values were in great agreement with the actual values, signifying the applicability of response surface methodology in the photocatalytic decolorization of dyeing effluents. The results gained from this research demonstrated that the synthesis method of trimetallic nanocomposite (Iron Triad) is a cost-effective and energy efficient method that can be scaled up to a higher level for industrial application. Full article
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Figure 1
<p>Synthesis of Fe-Ni-Co nanocomposite.</p>
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<p>SEM images of trimetallic nanocomposites at different magnification (<b>a</b>) 200 µm, (<b>b</b>) 100 µm, (<b>c</b>) 5 µm and (<b>d</b>) 1 µm.</p>
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<p>(<b>a</b>) The EDS-layered image shows the uniform distribution of the metals Fe, Ni and Co in nanocomposites. The separate diagram for each element including Fe, Ni, and Co is shown in (<b>b</b>), (<b>c</b>) and (<b>d</b>), respectively. (<b>e</b>) shows the EDS spectra and (<b>f</b>) illustrates the composition of the trimetallic nanocomposite.</p>
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<p>XRD pattern of trimetallic (Fe-Ni-Co) nanocomposite.</p>
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<p>FTIR spectra of trimetallic nanocomposite (<b>a</b>) and expended FTIR spectral region from 800 to 400 cm<sup>−1</sup> (<b>b</b>).</p>
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<p>Schematic overview of photocatalysis.</p>
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<p>RSM plots showing the percentage degradation of MO and the interaction between selected variables. (<b>a</b>) The effect of dye concentration and time; (<b>b</b>) the effect of dye concentration and pH; (<b>c</b>) effect of dye concentration and dose; (<b>d</b>) effect of dye concentration and hydrogen peroxide; (<b>e</b>) effect of dye concentration and temperature; (<b>f</b>) effect of time and pH; (<b>g</b>) effect of time and dose; (<b>h</b>) effect of time and hydrogen peroxide; (<b>i</b>) effect of time and temperature; (<b>j</b>) effect of pH and dose; (<b>k</b>) effect of pH and hydrogen peroxide; (<b>l</b>) effect of pH and temperature; (<b>m</b>) effect of dose and hydrogen peroxide; (<b>n</b>) effect of dose and temperature; (<b>o</b>) effect of hydrogen peroxide and temperature.</p>
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<p>Comparison between the predicted and actual degradation of MO.</p>
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22 pages, 10866 KiB  
Article
Catalytic Properties of Pd Deposited on Polyaniline in the Hydrogenation of Quinoline
by Olena O. Kompaniiets, Vladyslav V. Subotin, Andrii S. Poturai, Aleksandr A. Yurchenko, Alina A. Gorlova, Igor B. Bychko, Igor Ye. Kotenko, Olena O. Pariiska, Serhiy V. Ryabukhin, Dmytro M. Volochnyuk and Sergey V. Kolotilov
Chemistry 2024, 6(4), 738-759; https://doi.org/10.3390/chemistry6040044 (registering DOI) - 14 Aug 2024
Viewed by 201
Abstract
A set of Pd-containing composites was prepared by the deposition of Pd on the following carriers: polyaniline (PANI); PANI doped by H2SO4; Norit GSX activated carbon or Aerosil (SiO2) coated by PANI or by H2SO [...] Read more.
A set of Pd-containing composites was prepared by the deposition of Pd on the following carriers: polyaniline (PANI); PANI doped by H2SO4; Norit GSX activated carbon or Aerosil (SiO2) coated by PANI or by H2SO4-doped PANI; PANI after thermal treatment at 300 °C in an atmosphere of H2. One sample was also prepared by the in situ polymerization of aniline in the presence of Pd2+· The decomposition of Pd was carried out via deposition from the solutions of Pd2+ salts or decomposition of Pd0 complex Pd2(dba)3, where dba is dibenzylideneacetone. The composites were studied by powder X-ray diffraction, transmission electron microscopy, IR and Raman spectroscopy. The hydrogenation of quinoline in the presence of composites was carried out; the catalytic performance of the composites was evaluated by the yield of 1,2,3,4-tetrahydroquinoline. It was found that the doping of PANI by H2SO4, inclusion of Norit GSX activated carbon as a component of the carrier or thermal treatment of PANI prior to the deposition of Pd led to significant increase in the catalytic performance of the composites in the hydrogenation of quinoline. Full article
(This article belongs to the Section Catalysis)
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Graphical abstract

Graphical abstract
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<p>Structure of PANI. The x:y ratio can vary depending on the polymer formation conditions.</p>
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<p>Schematic synthesis of sample P1. The content of Pd determined by AAS is shown for convenience.</p>
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<p>Schematic synthesis of samples P2–P7. Carriers are marked by red, while Pd-containing composites are marked by blue. Contents of Pd determined by AAS are shown for convenience.</p>
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<p>Schematic synthesis of samples P8–P11, which contain PANI and additional carriers. Carriers are marked by red, while Pd-containing composites are marked by blue. Contents of Pd determined by AAS are shown for convenience.</p>
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<p>IR spectra of PANI and P1–P3 (the composites, formed upon the in situ polymerization of aniline or PANI treatment with aqueous solutions).</p>
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<p>IR spectra of PANI and P4 (the composite, formed upon Pd deposition on PANI via the decomposition of Pd<sub>2</sub>(dba)<sub>3</sub>).</p>
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<p>IR spectra of PANI-H<sub>2</sub>SO<sub>4</sub> and P6 (the composite, formed upon Pd deposition on PANI-H<sub>2</sub>SO<sub>4</sub> via the decomposition of Pd<sub>2</sub>(dba)<sub>3</sub>).</p>
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<p>IR spectra of PANI and PANI-300.</p>
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<p>IR spectra of PANI-300 and P7 (the composite, formed upon Pd deposition on PANI-300 via the decomposition of Pd<sub>2</sub>(dba)<sub>3</sub>).</p>
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<p>Raman spectra of the samples.</p>
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<p>TEM images of the selected samples.</p>
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<p>TEM images of the selected samples.</p>
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<p>Reaction used for evaluation of the catalytic properties of the composites.</p>
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<p>Yield of THQ vs. the Pd content in the reaction mixture (at p(H2) = 100 bar, T = 100 °C, 24 h, methanol). All samples containing PANI doped by H<sub>2</sub>SO<sub>4</sub> are marked by red color; samples containing C or PANI after thermal treatment are marked by blue (sample P11 contains both H<sub>2</sub>SO<sub>4</sub> and C, and it can be referred to in both these groups).</p>
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<p>The yields of the products (1,2,3,4-tetrahydroquinonile and 1-ethylnaphthalene) in the subsequent hydrogenation of quinoline and 1-ethynylnaphthalene, respectively, in the presence of the P11 (same sample was isolated and reused for the next runs). Conditions: p(H<sub>2</sub>) = 30 bar, T = 50 °C, methanol, 4 h. Pd loading was 1 mol.% for the first run.</p>
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11 pages, 2424 KiB  
Article
Nanocomposites of Natural Rubber Containing Montmorillonite Modified by Poly(2-oxazolines)
by Peter Boháč, Zuzana Nógellová, Miroslav Šlouf, Juraj Kronek, Ľuboš Jankovič, Hamed Peidayesh, Jana Madejová and Ivan Chodák
Materials 2024, 17(16), 4017; https://doi.org/10.3390/ma17164017 - 13 Aug 2024
Viewed by 237
Abstract
Nanocomposites with a natural rubber (NR) matrix containing organomodified montmorillonite (MMT) as a precursor of nanoparticles were prepared using two different polyoxazolines as surface modifiers of the MMT. The materials were characterized by X-ray diffraction, transmission electronic microscopy and ultimate mechanical properties, and [...] Read more.
Nanocomposites with a natural rubber (NR) matrix containing organomodified montmorillonite (MMT) as a precursor of nanoparticles were prepared using two different polyoxazolines as surface modifiers of the MMT. The materials were characterized by X-ray diffraction, transmission electronic microscopy and ultimate mechanical properties, and parameters obtained by DMTA method (storage and loss moduli and loss tangent) were determined. It was found that the effect of nanofillers presence has a significant effect on tensile strength as well as elongation at break, which are higher for materials with higher viscosity due to the presence of carbon blacks compared to the composites without carbon blacks. From the two modifiers, poly(2-ethyl-2-oxazoline) was identified as a prospective modifier for surface modification of MMT used as the possible additive for tyre treads exhibiting optimal balance between fuel consumption and safety of driving concerning breaking action and lateral breakaway. Full article
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<p>Chemical structures of poly(2-ethyl-2-oxazoline) (PEtOx) and statistical copolymer poly(2-ethyl-2-oxazoline-co-ethyleneimine) (PETOX-PEI).</p>
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<p>Scheme of synthesis of poly(2-ethyl-2-oxazoline) (PETOX) and statistical copolymer poly(2-ethyl-2-oxazoline-co-ethyleneimine) (PETOX-PEI).</p>
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<p>The XRD records of the NR vulcanizates without carbon blacks (left-hand side) and with 20 phr of N-550 carbon blacks (right-hand side) filled with 3 wt % of MMT modified with various amounts of modifiers, 1—no MMT, 2—100 meq of PEI-PETOX copolymer, 3—300 meq of PEI-PETOX copolymer, 4—100 meq of PETOX, 5—300 meq of PETOX.</p>
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<p>Examples of TEM micrographs showing typical morphologies in NR vulcanizates for samples of NR with 3 phr of MMT modified by PETOX100 both without (<b>a</b>–<b>c</b>) and with (<b>d</b>–<b>e</b>) carbon black. All samples, regardless of their modification, contained MMT in the form of large particles (<b>a</b>,<b>d</b>), smaller agglomerates (<b>b</b>,<b>e</b>), and exfoliated platelets (<b>c</b>,<b>f</b>). In contrast, the carbon black particles were homogeneously dispersed in all investigated samples (<b>d</b>–<b>f</b>).</p>
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<p>The DMTA records of the NR vulcanizates without carbon blacks (left-hand side) and with 20 phr of N-550 carbon blacks (right-hand side) filled with 3 wt% of MMT modified with various amounts of modifiers, black—no MMT, red—100 meq of PEI-PETOX copolymer, blue—300 meq of PEI-PETOX copolymer, green—100 meq of PETOX, orange—300 meq of PETOX.</p>
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15 pages, 3885 KiB  
Article
Green Synthesis of Cobalt-Doped CeFe2O5 Nanocomposites Using Waste Gossypium arboreum L. Stalks and Their Application in the Removal of Toxic Water Pollutants
by Saloni Koul, Mamata Singhvi and Beom Soo Kim
Nanomaterials 2024, 14(16), 1339; https://doi.org/10.3390/nano14161339 - 12 Aug 2024
Viewed by 365
Abstract
Currently, there is an increasing need to find new ways to purify water by eliminating bacterial biofilms, textile dyes, and toxic water pollutants. These contaminants pose significant risks to both human health and the environment. To address this issue, in this study, we [...] Read more.
Currently, there is an increasing need to find new ways to purify water by eliminating bacterial biofilms, textile dyes, and toxic water pollutants. These contaminants pose significant risks to both human health and the environment. To address this issue, in this study, we have developed an eco-friendly approach that involves synthesizing a cobalt-doped cerium iron oxide (CCIO) nanocomposite (NC) using an aqueous extract of Gossypium arboreum L. stalks. The resulting nanoparticles can be used to effectively purify water and tackle the challenges associated with these harmful pollutants. Nanoparticles excel in water pollutant removal by providing a high surface area for efficient adsorption, versatile design for the simultaneous removal of multiple contaminants, catalytic properties for organic pollutant degradation, and magnetic features for easy separation, offering cost-effective and sustainable water treatment solutions. A CCIO nanocomposite was synthesized via a green co-precipitation method utilizing biomolecules and co-enzymes extracted from the aqueous solution of Gossypium arboreum L. stalk. This single-step synthesis process was accomplished within a 5-h reaction period. Furthermore, the synthesis of nanocomposites was confirmed by various characterization techniques such as Fourier-transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), dynamic light scattering (DLS), and energy dispersive X-ray (EDX) technology. CCIO NCs were discovered to have a spherical shape and an average size of 40 nm. Based on DLS zeta potential analysis, CCIO NCs were found to be anionic. CCIO NCs also showed significant antimicrobial and antioxidant activity. Overall, considering their physical and chemical properties, the application of CCIO NCs for the adsorption of various dyes (~91%) and water pollutants (chromium = ~60%) has been considered here since they exhibit great adsorption capacity owing to their microporous structure, and represent a step forward in water purification. Full article
(This article belongs to the Special Issue Nanomaterials in Water Applications)
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<p>Illustration of the application of synthesized CCIO NCs in water pollutant removal.</p>
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<p>Characterization of CCIO NCs using (<b>A</b>) SEM, (<b>B</b>) TEM, (<b>C</b>) EDX, (<b>D</b>) FTIR, (<b>E</b>) zeta potential, and (<b>F</b>) XRD.</p>
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<p>UV-Vis spectra of: (<b>A</b>) SF at different concentrations (1–5 mg/mL), (<b>B</b>) MG at different concentrations (1–5 mg/mL), (<b>C</b>) MB at (1–5 mg/mL), and (<b>D</b>) the regeneration efficiency (%) of CCIO NCs using SF, MG, and MB dyes.</p>
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<p>UV-Vis spectra for analyzing the adsorption capacity of CCIO NPs against chromium (<span class="html-small-caps">VI</span>).</p>
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<p>UV-Vis spectra of SF, MG, and MB at 10 mg/mL concentration.</p>
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<p>Antioxidant activity of CCIO NCs at different concentrations (1–5 mg/mL).</p>
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<p>Antimicrobial activity of synthesized CCIO NPs against <span class="html-italic">E. coli</span> and <span class="html-italic">S. aureus</span>.</p>
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<p>Regeneration efficiency of reused CCIO NCs, using SF dye.</p>
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<p>Plausible mechanism of action of CCIO NCs in dye adsorption.</p>
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18 pages, 3926 KiB  
Review
The Development of Polylactide Nanocomposites: A Review
by Purba Purnama, Zaki Saptari Saldi and Muhammad Samsuri
J. Compos. Sci. 2024, 8(8), 317; https://doi.org/10.3390/jcs8080317 - 10 Aug 2024
Viewed by 260
Abstract
Polylactide materials present a promising alternative to petroleum-based polymers due to their sustainability and biodegradability, although they have certain limitations in physical and mechanical properties for specific applications. The incorporation of nanoparticles, such as layered silicate (clay), carbon nanotubes, metal or metal oxide, [...] Read more.
Polylactide materials present a promising alternative to petroleum-based polymers due to their sustainability and biodegradability, although they have certain limitations in physical and mechanical properties for specific applications. The incorporation of nanoparticles, such as layered silicate (clay), carbon nanotubes, metal or metal oxide, cellulose nanowhiskers, can address these limitations by enhancing the thermal, mechanicals, barriers, and some other properties of polylactide. However, the distinct characteristics of these nanoparticles can affect the compatibility and processing of polylactide blends. In the polylactide nanocomposites, well-dispersed nanoparticles within the polylactide matrix result in excellent mechanical and thermal properties of the materials. Surface modification is required to improve compatibility and the crystallization process in the blended materials. This article reviews the development of polylactide nanocomposites and their applications. It discusses the general aspect of polylactides and nanomaterials as nanofillers, followed by the discussion of the processing and characterization of polylactide nanocomposites, including their applications. The final section summarizes and discusses the future challenges of polylactide nanocomposites concerning the future material’s requirements and economic considerations. As eco-friendly materials, polylactide nanocomposites offer significant potential to replace petroleum-based polymers. Full article
(This article belongs to the Special Issue Sustainable Biocomposites, Volume II)
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<p>The chemical structure of lactide stereoisomers.</p>
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<p>FTIR spectra of PDLLA/hydroxyapatite nanocomposites at various weight ratios (3:1, 2:1, 1:1) (<b>a</b>); magnified FTIR spectra at section A (<b>b</b>) and section B (<b>c</b>); schematic model of hydrogen bonding between PDLLA and hydroxyapatite particles (<b>d</b>). Adapted with permission [<a href="#B31-jcs-08-00317" class="html-bibr">31</a>]. Copyright 2007 American Chemical Society.</p>
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<p>WAXD diffractogram of various organoclays with C16 organic modifiers. Adapted with permission [<a href="#B9-jcs-08-00317" class="html-bibr">9</a>]. Copyright 2002 American Chemical Society.</p>
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<p>The most commonly used nanofillers in polymer nanocomposites and their properties. Adapted with permission [<a href="#B7-jcs-08-00317" class="html-bibr">7</a>]. Copyright 2012 American Chemical Society.</p>
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<p>The schematic illustration structure of polymer nanocomposities using layered silicate nanoparticles [<a href="#B55-jcs-08-00317" class="html-bibr">55</a>]. (Copyright and permission, Elsevier 2003).</p>
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<p>Transmission electron micrograph of acetylated cellulose nanowhiskers (<b>a</b>). FT-IR spectra of acetylated cellulose nanowhiskers, PDLA and PDLA-g-cellulose nanowhiskers (<b>b</b>) [<a href="#B77-jcs-08-00317" class="html-bibr">77</a>]. (Copyright and permission, Springer Nature 2014).</p>
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28 pages, 3497 KiB  
Review
Polymer-Assisted Graphite Exfoliation: Advancing Nanostructure Preparation and Multifunctional Composites
by Jaime Orellana, Esteban Araya-Hermosilla, Andrea Pucci and Rodrigo Araya-Hermosilla
Polymers 2024, 16(16), 2273; https://doi.org/10.3390/polym16162273 - 10 Aug 2024
Viewed by 514
Abstract
Exfoliated graphite (ExG) embedded in a polymeric matrix represents an accessible, cost-effective, and sustainable method for generating nanosized graphite-based polymer composites with multifunctional properties. This review article analyzes diverse methods currently used to exfoliate graphite into graphite nanoplatelets, few-layer graphene, and polymer-assisted graphene. [...] Read more.
Exfoliated graphite (ExG) embedded in a polymeric matrix represents an accessible, cost-effective, and sustainable method for generating nanosized graphite-based polymer composites with multifunctional properties. This review article analyzes diverse methods currently used to exfoliate graphite into graphite nanoplatelets, few-layer graphene, and polymer-assisted graphene. It also explores engineered methods for small-scale pilot production of polymer nanocomposites. It highlights the chemistry involved during the graphite intercalation and exfoliation process, particularly emphasizing the interfacial interactions related to steric repulsion forces, van der Waals forces, hydrogen bonds, π-π stacking, and covalent bonds. These interactions promote the dispersion and stabilization of the graphite derivative structures in polymeric matrices. Finally, it compares the enhanced properties of nanocomposites, such as increased thermal and electrical conductivity and electromagnetic interference (EMI) shielding applications, with those of neat polymer materials. Full article
(This article belongs to the Special Issue Functional Graphene-Polymer Composites)
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<p>Graphite structures and sources.</p>
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<p>SEM micrographs of rolling intercalation PS with 5% of colloidal graphite [<a href="#B27-polymers-16-02273" class="html-bibr">27</a>]. Reproduced with permission from Tu, H.; Polymers for advanced technologies; Published by John/Wiley &amp; Sons Ltd.; 2008.</p>
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<p>Orientation of the graphite platelet structures in extruded strands: (left) schematic figure of platelet orientation along strand flow direction by extrusion out of the die; and (right) transmission light microscopy pictures of samples cut perpendicular to the strand direction (shows mainly the layer thickness) and cut parallel to the long-axis of the strand (shows the lateral dimension of visible GNP structures), here shown for 1 wt% Graphene nanopowder AO-3 in PC [<a href="#B124-polymers-16-02273" class="html-bibr">124</a>]. Reproduced with permission from Pötschke, P.; Materials; Published by MDPI; 2017.</p>
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<p>SEM images of (<b>a</b>) PVDF/expanded graphite composite fabricated without water (P-EG) and (<b>b</b>) PVDF/expanded graphite composite fabricated with water (P-EG-W) samples [<a href="#B91-polymers-16-02273" class="html-bibr">91</a>]. Reproduced with permission from Tong, J.; Macromolecular materials and engineering; Published by Wiley-VCH Verlag GMBH &amp; Co.; 2020.</p>
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<p>FESEM images of (<b>A</b>) PCGF-30 [<a href="#B87-polymers-16-02273" class="html-bibr">87</a>]. Reproduced with permission from Pradhan, S.S.; Polymer composites; Published by John/Wiley &amp; Sons Ltd.; 2021.</p>
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<p>SEM images of graphite at magnifications of 15 and 150 Kx at different ball milling times: (<b>a</b>,<b>b</b>) 0 h; (<b>c</b>,<b>d</b>) 1 h; (<b>e</b>,<b>f</b>) 4 h; (<b>g</b>,<b>h</b>) 8 h; (<b>i</b>,<b>j</b>) 16 h [<a href="#B130-polymers-16-02273" class="html-bibr">130</a>]. Reproduced with permission from Visco, A.; Polymers; Published by MDPI; 2021.</p>
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<p>EMI-S effectiveness (dB) and wt% filler in different matrix.</p>
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<p>Thermal conductivity and wt% filler in different matrix, conductive nanocomposite.</p>
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<p>Thermal conductivity and wt% filler in different matrices, conductive nanocomposite.</p>
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<p>Engineering state-of-the-art techniques to generate exfoliated graphite/polymers composites.</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, 8501 KiB  
Article
Investigation of the Electrochemical Behavior of CuO-NiO-Co3O4 Nanocomposites for Enhanced Supercapacitor Applications
by Karthik Kannan, Karuppaiya Chinnaiah, Krishnamoorthy Gurushankar, Raman Krishnamoorthi, Yong-Song Chen, Paskalis Sahaya Murphin Kumar and Yuan-Yao Li
Materials 2024, 17(16), 3976; https://doi.org/10.3390/ma17163976 - 10 Aug 2024
Viewed by 348
Abstract
In the present study, composites incorporating NiO-Co3O4 (NC) and CuO-NiO-Co3O4 (CNC) as active electrode materials were produced through the hydrothermal method and their performance was investigated systematically. The composition, formation, and nanocomposite structure of the fabricated material [...] Read more.
In the present study, composites incorporating NiO-Co3O4 (NC) and CuO-NiO-Co3O4 (CNC) as active electrode materials were produced through the hydrothermal method and their performance was investigated systematically. The composition, formation, and nanocomposite structure of the fabricated material were characterized by XRD, FTIR, and UV–Vis. The FE-SEM analysis revealed the presence of rod and spherical mixed morphologies. The prepared NC and CNC samples were utilized as supercapacitor electrodes, demonstrating specific capacitances of 262 Fg−1 at a current density of 1 Ag−1. Interestingly, the CNC composite displayed a notable long-term cyclic stability 84.9%, which was observed even after 5000 charge–discharge cycles. The exceptional electrochemical properties observed can be accredited to the harmonious effects of copper oxide addition, the hollow structure, and various metal oxides. This approach holds promise for the development of supercapacitor electrodes. These findings collectively indicate that the hydrothermally synthesized NC and CNC nanocomposites exhibit potential as high-performance electrodes for supercapacitor applications. Full article
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<p>XRD pattern of hydrothermally synthesized (<b>a</b>) NC and (<b>b</b>) CNC nanocomposites.</p>
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<p>(<b>a</b>,<b>b</b>) FE-SEM images of the CNC composite with high and low magnifications, (<b>c</b>) EDAX spectrum with composition analysis table of the NC nanocomposite.</p>
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<p>(<b>a</b>,<b>b</b>) FE-SEM images of the CNC composite with high and low magnifications, (<b>c</b>) EDAX spectrum with composition analysis table of the CNC nanocomposite.</p>
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<p>EDS mapping of the CNC composite’s overall spectrum: (<b>a</b>,<b>b</b>), oxygen (<b>c</b>), cobalt (<b>d</b>), nickel (<b>e</b>), and copper (<b>f</b>), respectively.</p>
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<p>UV–vis absorbance spectrum (<b>a</b>) and (<b>b</b>) optical bandgap of the prepared CNC nanocomposite.</p>
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<p>CV curves of (<b>a</b>) NC, (<b>b</b>) CNC composites, (<b>c</b>) calculated specific capacitance variation against the scan rates for NC and CNC electrodes.</p>
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<p>Redox peak relationships: (<b>a</b>) NC, (<b>b</b>) CNC composites, (<b>c</b>) magnitude variation of current in CV curves, (<b>d</b>,<b>e</b>) determined b-values for NC and CNC composites.</p>
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<p>Specific capacitance contributions versus scan rates (<b>a</b>) NC, (<b>b</b>) CNC electrodes, (<b>c</b>,<b>d</b>) Resultant specific capacitances at a scan rate of 25 mVs<sup>−1</sup> for NC and CNC.</p>
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<p>(<b>a</b>,<b>b</b>) GCD curves, (<b>c</b>,<b>d</b>) corresponding values of specific capacitance, and (<b>e</b>,<b>f</b>) cyclic retention and Coulombic efficiency of NC and CNC electrodes.</p>
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<p>(<b>a</b>,<b>b</b>) EIS analysis of the prepared NC and CNC composites, (<b>c</b>,<b>d</b>) corresponding phase angles.</p>
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<p>Schematic representation of hydrothermally prepared CNC nanocomposite.</p>
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17 pages, 4274 KiB  
Article
ZnO–Graphene Oxide Nanocomposite for Paclitaxel Delivery and Enhanced Toxicity in Breast Cancer Cells
by Lorenzo Francesco Madeo, Christine Schirmer, Giuseppe Cirillo, Ayah Nader Asha, Rasha Ghunaim, Samuel Froeschke, Daniel Wolf, Manuela Curcio, Paola Tucci, Francesca Iemma, Bernd Büchner, Silke Hampel and Michael Mertig
Molecules 2024, 29(16), 3770; https://doi.org/10.3390/molecules29163770 - 9 Aug 2024
Viewed by 398
Abstract
A ZnO-Graphene oxide nanocomposite (Z-G) was prepared in order to exploit the biomedical features of each component in a single anticancer material. This was achieved by means of an environmentally friendly synthesis, taking place at a low temperature and without the involvement of [...] Read more.
A ZnO-Graphene oxide nanocomposite (Z-G) was prepared in order to exploit the biomedical features of each component in a single anticancer material. This was achieved by means of an environmentally friendly synthesis, taking place at a low temperature and without the involvement of toxic reagents. The product was physicochemically characterized. The ZnO-to-GO ratio was determined through thermogravimetric analysis, while scanning electron microscopy and transmission electron microscopy were used to provide insight into the morphology of the nanocomposite. Using energy-dispersive X-ray spectroscopy, it was possible to confirm that the graphene flakes were homogeneously coated with ZnO. The crystallite size of the ZnO nanoparticles in the new composite was determined using X-ray powder diffraction. The capacity of Z-G to enhance the toxicity of the anticancer drug Paclitaxel towards breast cancer cells was assessed via a cell viability study, showing the remarkable anticancer activity of the obtained system. Such results support the potential use of Z-G as an anticancer agent in combination with a common chemotherapeutic like Paclitaxel, leading to new chemotherapeutic formulations. Full article
(This article belongs to the Special Issue Carbon Materials in Materials Chemistry—2nd Edition)
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<p>TGA of GO, ZnO NPs, Z-G, and Z-G*.</p>
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<p>FTIR spectra of GO, ZnO NPs, Z-G and Z-G*.</p>
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<p>pXRD pattern of ZnO NPs, Z-G, and Z-G*.</p>
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<p>SEM (<b>a</b>,<b>b</b>) and TEM (<b>c</b>–<b>e</b>) images of Z-G* (<b>a</b>) and Z-G (<b>b</b>–<b>e</b>). (<b>c</b>) Bright-field TEM (BFTEM) image of ZnO NPs clusters on GO sheets. The wrinkling of the latter is visible as dark lines. (<b>d</b>) BFTEM images at higher magnification showing morphology, size, and arrangement of the ZnO NPs within the cluster. (<b>e</b>) High-resolution TEM (HRTEM) images of ZnO NPs at the edge of the cluster showing lattice planes at a few NPs. (<b>f</b>) Fourier transform of (<b>e</b>) revealing reflections of both ZnO and GO.</p>
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<p>EDX mapping of Z-G* (<b>a</b>–<b>d</b>) and Z-G (<b>e</b>–<b>h</b>). The original SEM images are shown in (<b>a</b>,<b>e</b>). The detected elements were O (<b>b</b>,<b>f</b>), C (<b>c</b>,<b>g</b>), and Zn (<b>d</b>,<b>h</b>). Scale bar = 1 μm.</p>
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<p>Ptx release profiles for Z-G, GO, and ZnO NP samples.</p>
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<p>Cancer cells’ viability after 48 h of incubation with unloaded NPs (GO, Z-G), Ptx, and loaded NPs (ZnO/Ptx, GO/Ptx, and Z-G/Ptx) compared to the control (DMSO treatment). ***/**/* decreased viability vs. control (DMSO); ###/##/# decreased viability vs unloaded NPs; +++/++ decreased viability vs Ptx; */# <span class="html-italic">p</span> &lt; 0.05; **/##/++ <span class="html-italic">p</span> &lt; 0.01; ***/###/+++ <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Light microscopy images of cancer cells treated with Ptx (50 μg/mL) and Z-G/Ptx (25 μg/mL) for 48 h. Scale bar = 100 µm.</p>
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33 pages, 10474 KiB  
Review
A Review on the Advances in Nanomaterials for Electrochemical Non-Enzymatic Glucose Sensors Working in Physiological Conditions
by Velia Osuna, Eider Pedro Aparicio Martínez, Rocio B. Dominguez and Alejandro Vega Rios
Chemosensors 2024, 12(8), 159; https://doi.org/10.3390/chemosensors12080159 - 8 Aug 2024
Viewed by 336
Abstract
Although an enzymatic electrochemical biosensor is a major keystone in Diabetes Mellitus management, its replacement with a low-cost and stable non-enzymatic glucose sensor (NEGS) is of high interest to scientific and industrial fields. However, most NEGS for direct glucose electrooxidation (DGE) must be [...] Read more.
Although an enzymatic electrochemical biosensor is a major keystone in Diabetes Mellitus management, its replacement with a low-cost and stable non-enzymatic glucose sensor (NEGS) is of high interest to scientific and industrial fields. However, most NEGS for direct glucose electrooxidation (DGE) must be performed under extreme alkaline conditions, implying additional pretreatments before detection and a limited application for on-body, real-time monitoring. Thus, research on DGE in physiological conditions is fundamental to successfully translating the current NEGS into clinical applications. In physiological conditions, drawbacks such as low current, low selectivity, and poisoning appear due to the reduction of OH ions in neutral electrolytes and the presence of chloride ions in biofluids. Therefore, an increasing number of nanomaterials based on Pt, Au, and their nanocomposites have been proposed to improve the electrochemical performance. Additionally, transition metals such as Cu, Pd, Ni, or Co combined with high surface area supports have shown promising results in increasing catalytic sites for DGE. The molecular interaction of phenylboronic acid with glucose has also been demonstrated in neutral conditions. Overall, the present review summarizes the current strategies for DGE in physiological conditions and highlights the challenges still faced for further development of functional glucose NEGS. Full article
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<p>(<b>a</b>) Global prevalence of diabetes in the 20–79 year age group (millions) from 2000 to 2021. (<b>b</b>) Projections of the global prevalence of diabetes in the 20–79 year age group (millions). Reprinted from [<a href="#B2-chemosensors-12-00159" class="html-bibr">2</a>] according to data from the International Diabetes Federation (IDF), under a Creative Commons Attribution 4.0 International License.</p>
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<p>Publication trend of scientific papers in the field of electrochemical glucose detection from 1981 to 2023 using Scopus (keywords: glucose non-enzymatic sensor, electrochemical, and neutral pH); blue bars indicate the works in non-enzymatic detection with alkaline electrolytes, the pink bars represent the published works using enzymatic detection, and the green bars include the reported non-enzymatic glucose sensors at physiological conditions.</p>
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<p>Diagram of the effect of (<b>a</b>) interference with the glucose measurement, and (<b>b</b>) poisoning on the electrode.</p>
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<p>Mechanism of glucose electrooxidation using the Pt electrode according to Ernst and Heitbaum [<a href="#B41-chemosensors-12-00159" class="html-bibr">41</a>,<a href="#B42-chemosensors-12-00159" class="html-bibr">42</a>]. (<b>a</b>) Hydrogen region. (<b>b</b>) Double-layer region.</p>
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<p>Mechanism of DGE (direct glucose electrooxidation) using the Au electrode. 1. Au work electrode; 2. Adsorption of OH<sup>−</sup> on surface ((OH)<sub>ads</sub>); 3. Interaction between the hemiacetal group of glucose and (OH)<sub>ads</sub>; 4. Gluconolactone generation.</p>
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<p>Mechanism of interaction between glucose and phenylboronic acid (PBA) at neutral pH. 1. Phenylboronic acid (PBA) or its derivates; 2. Conformational changes to sp<sup>3</sup> hybridized boronates in aqueous media; 3. Reversible covalent bonds between the boron atom and the hydroxyl groups (1,2 and 1,3 diols) of the glucose; 4. Formation of a boronate ester, a stable complex between PBA and glucose.</p>
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<p>SEM micrographs of (<b>a</b>) Boron-doped diamond (BDD), (<b>b</b>) Ni-BDD, (<b>c</b>) Pt-BDD, (<b>d</b>) PtNi-BDD, (<b>e</b>) Pt/Ni-BDD, and (<b>f</b>) Ni/Pt BDD. CVs response of (<b>g</b>) PtNi-BDD, (<b>h</b>) Magnification of the oxidation peaks at different glucose concentrations of PtNi-BDD (<b>g</b>), (<b>i</b>) Pt-BDD, (<b>j</b>) Ni/Pt-BDD, and (<b>k</b>) Pt/Ni-BDD analyzed under different glucose concentrations (2, 4, 5, 9, and 12 mM) at a pH of 7.4 (0.01 M PBS). (<b>l</b>) Linear calibration relations of the current response vs. glucose concentration [<a href="#B68-chemosensors-12-00159" class="html-bibr">68</a>]. Reprinted (adapted) with permission from [<a href="#B68-chemosensors-12-00159" class="html-bibr">68</a>] Copyright © 2023 with permission from Elsevier.</p>
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<p>(<b>a</b>) Amperometric response to a wide range of glucose concentrations in PBS [0.1 M]. (<b>b</b>) Calibration plot of sensor Au@Pt/Au/Nafion at +0.35 V (Ag/AgCl). (<b>c</b>) Amperometric response for the interference effects of other bio-compounds on the sensor probe. (<b>d</b>) Stability test for 27 days, and the test conditions were PBS [0.1 M] containing 1.0 mM glucose (Note: the electrode was stored at room temperature in a dry state when not in use). Reprinted (adapted) with permission from [<a href="#B100-chemosensors-12-00159" class="html-bibr">100</a>] Copyright © 2023 with permission from Elsevier.</p>
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<p>(<b>a</b>) Scheme of Pd/Au NC synthesis and its HAADF-STEM images. (<b>b</b>) Scheme of Pd/Pt concave nanocube (CNC) synthesis and its HAADF-STEM images; (<b>c</b>) amperometric responses from 0.25 mM to 1 mM; (<b>d</b>) interference studies; (<b>e</b>) calibration curves; (<b>f</b>) real sample experiments. Reprinted (adapted) with permission from [<a href="#B48-chemosensors-12-00159" class="html-bibr">48</a>] Copyright © 2023 with permission from Elsevier.</p>
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<p>TEM micrographs of the CuNWs/MOF/GO sensor: (<b>a</b>) CuNWs, (<b>b</b>) GO, (<b>c</b>) MOF, and (<b>d</b>) a fully assembled nanocomposite; (<b>e</b>) the amperometric I vs. t curve obtained at 0.3 V with the assembled CuNWs/MOF/GO sensor working in 0.1 M PBS, and (<b>f</b>) the calibration curve. Reprinted (adapted) with permission from [<a href="#B105-chemosensors-12-00159" class="html-bibr">105</a>] Copyright © 2018 with permission from Elsevier; (<b>g</b>) the preparation of the Co<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub> nanoflowers/SPCE sensor and its response towards glucose oxidation in 0.01 M PBS at a pH of 7.4. Reprinted (adapted) with permission from [<a href="#B102-chemosensors-12-00159" class="html-bibr">102</a>] Copyright © 2018 with permission from American Chemical Society.</p>
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<p>(<b>a</b>) The assembly of the GCE/PAA-Au-NPs-MPBA sensor with the blockage of the surface after glucose capture. Reprinted (adapted) with permission from [<a href="#B54-chemosensors-12-00159" class="html-bibr">54</a>] Copyright © 2017 with permission from Elsevier; (<b>b</b>) synthesis of mesoporous silica adding PBA for surface functionalization; (<b>c</b>) set up for recording the interaction of glucose with the Ta<sub>2</sub>O<sub>5</sub>/MPSi-PBA sensor and the corresponding response after the glucose addition compared to the minimal response at unmodified PBA surfaces. (<b>d</b>) Reprinted (adapted) with permission from [<a href="#B113-chemosensors-12-00159" class="html-bibr">113</a>] Copyright © 2021 with permission from American Chemical Society.</p>
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<p>Fabrication of a carbon cloth electrode modified with AuNF showing the nanostructures deposed on the textile fibers: the fabrication of the CC-AuNFs with space gauze in between electrodes (<b>a</b>–<b>d</b>), and a SEM image of active AuNF over the CC fibers. Reprinted (adapted) with permission from [<a href="#B60-chemosensors-12-00159" class="html-bibr">60</a>] Copyright © 2023 with permission from Elsevier; (<b>e</b>) fabrication of the patch-like rGO/PU-Au wearable sensor showing the molding of the base electrode and the subsequent surface modifications (FE-SEM micrographs of rGO/PU-Au); the inset photograph showed the on-body recording obtained by the rGO/PU-Au sweat glucose detection after and before a meal. Reprinted (adapted) with permission from [<a href="#B62-chemosensors-12-00159" class="html-bibr">62</a>] Copyright © 2019 with permission from American Chemical Society; (<b>f</b>) the integration of the PdNPs/Co-ZIF-67 sensor in a wearable sweatband with a miniaturized reader; (<b>g</b>) on-body detection and recording of results in a smartphone app; (<b>h</b>) recorded trend of the PdNPs/Co-ZIF-67 wearable sensor for sweat glucose compared to blood glucose. Reprinted (adapted) with permission from [<a href="#B58-chemosensors-12-00159" class="html-bibr">58</a>] Copyright © 2019 with permission from American Chemical Society.</p>
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19 pages, 3920 KiB  
Article
Influence of the Processing Conditions on the Rheology and Heat of Decomposition of Solution Processed Hybrid Nanocomposites and Implication to Sustainable Energy Storage
by Andekuba Andezai and Jude O. Iroh
Energies 2024, 17(16), 3930; https://doi.org/10.3390/en17163930 - 8 Aug 2024
Viewed by 365
Abstract
This study investigates the properties of solution-processed hybrid polyimide (PI) nanocomposites containing a variety of nanofillers, including polyaniline copolymer-modified clay (PNEA), nanographene sheets (NGSs), and carbon nanotube sheets (CNT-PVDFs). Through a series of experiments, the flow behavior of poly(amic acid) (PAA) solution and [...] Read more.
This study investigates the properties of solution-processed hybrid polyimide (PI) nanocomposites containing a variety of nanofillers, including polyaniline copolymer-modified clay (PNEA), nanographene sheets (NGSs), and carbon nanotube sheets (CNT-PVDFs). Through a series of experiments, the flow behavior of poly(amic acid) (PAA) solution and PAA suspension containing polyaniline copolymer-modified clay (PNEA) is determined as a function of the shear rate, processing temperature, and polymerization time. It is shown that the neat PAA solution exhibits a complex rheological behavior ranging from shear thickening to Newtonian behavior with increasing shear rate and testing temperature. The presence of modified clay in PAA solution significantly reduced the viscosity of PAA. Differential scanning calorimetry (DSC) analysis showed that polyimide–nanographene sheet (PI NGS) nanocomposites processed at a high spindle speed (100 rpm) have lower total heat of decomposition, which is indicative of improved fire retardancy. The effect of processing temperature on the specific capacitance of a polyimide–CNT-PVDF composite containing electrodeposited polypyrrole is determined using cyclic voltammetry (CV). It is shown that the hybrid composite working electrode material processed at 90 °C produces a remarkably higher overall stored charge when compared to the composite electrode material processed at 250 °C. Consequently, the specific capacitance obtained at a scan rate of 5 mV/s for the hybrid nanocomposite processed at 90 °C is around 858 F/g after one cycle, which is about 6.3 times higher than the specific capacitance of 136 F/g produced by the hybrid nanocomposite processed at 250 °C. These findings show that the properties of the hybrid nanocomposites are remarkably influenced by the processing conditions and highlight the need for process optimization. Full article
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<p>Schematic illustration of in situ synthesis of (<b>a</b>) PI/clay nanocomposite, (<b>b</b>) PI/graphene nanocomposite, and (<b>c</b>) solution casting of PAA/CNT-PVDF and (<b>d</b>) electrochemical synthesis of polypyrrole.</p>
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<p>Dependence of viscosity on the shear rate and temperature for neat PAA solution. The arrows mark the critical shear rates for transition from shear thickening to Newtonian behavior.</p>
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<p>Effect of temperature on the critical shear rate <math display="inline"><semantics> <mover accent="true"> <mi>γ</mi> <mo>˙</mo> </mover> </semantics></math><sub>c</sub> and steady-state viscosity for the neat poly(amic acid) solution.</p>
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<p>Effect of shear rate and temperature on the viscosity of poly(amic acid) suspension containing 5 wt.% of polyaniline copolymer-modified (PNEA) Cloisite 30B clay. The arrow marks the critical shear rate for transition from shear thickening to Newtonian behavior.</p>
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<p>Effect of shear rate and polymerization time on the viscosity of poly(amic acid) after 30 min and 24 h of polymerization. The arrows mark the critical shear rates for transition from shear thickening to Newtonian behavior.</p>
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<p>Plot of ln viscosity (cP) vs. inverse temperature <math display="inline"><semantics> <mrow> <mfenced> <mrow> <msup> <mi>K</mi> <mrow> <mo>−</mo> <mn>1</mn> </mrow> </msup> </mrow> </mfenced> </mrow> </semantics></math> at a spindle speed rate of 20 rpm for (i) neat PAA sample and (ii) PAA suspension containing 5 wt.% PNEA.</p>
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<p>Plot of (i) inherent viscosity and (ii) reduced viscosity against concentration for (<b>a</b>) PAA solution and (<b>b</b>) PAA suspension containing 5 wt.% PNEA modified clay.</p>
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<p>(<b>a</b>) DSC thermograms of (i) neat PI, (ii) PI-10 wt.% nanographene sheet sheared at 100 rpm for 30 min, and (iii) PI-10 wt.% nanographene sheet and (<b>b</b>) DSC curves of (i) neat PI, (ii) PI-40 wt.% nanographene sheet cast after shearing the suspension at 100 rpm for 30 min, and (iii) PI-40 wt.% nanographene sheet cast without additional shearing of the suspension. The DSC test was conducted under a nitrogen atmosphere at a heating rate of 5 °C/min.</p>
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<p>Cyclic voltammograms of PI/CNT-PVDF composites processed at (i) 90 °C and (ii) 250 °C followed by electrodeposition of PPy using a Ag/AgCl reference electrode and a graphite rod counter electrode for (<b>a</b>) 1 cycle and (<b>b</b>) 10 cycles; (<b>c</b>) composites processed at 90 °C for (i) 1 cycle and (ii) 10 cycles; and (<b>d</b>) composites processed at 250 °C for (i) 1 cycle and (ii) 10 cycles. CV was run at 5 mV/s.</p>
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<p>Cyclic voltammograms of PI/CNT-PVDF composites processed at (i) 90 °C and (ii) 250 °C followed by electrodeposition of PPy using a Ag/AgCl reference electrode and graphite rod counter electrode for (<b>a</b>) 1 cycle and (<b>b</b>) 10 cycles; (<b>c</b>) composites processed at 90 °C for (i) 1 cycle and (ii) 10 cycles; and (<b>d</b>) composites processed at 250 °C for (i) 1 cycle and (ii) 10 cycles. CV was run at 25 mV/s.</p>
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<p>Transient i–t curves obtained during potentiostatic polymerization of 0.5 M pyrrole in a 0.0225 M toluene sulphonic acid solution at an applied potential of 2 V onto PI/CNT-PVDF composite working electrodes processed at (i) 90 °C and (ii) 250 °C.</p>
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<p>Synthesis of polyimide (PI).</p>
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3 pages, 167 KiB  
Editorial
Exclusive Papers by the Editorial Board Members and Topical Advisory Panel Members of Catalysts in the “Photocatalysis” Section
by Jorge Bedia and Detlef W. Bahnemann
Catalysts 2024, 14(8), 509; https://doi.org/10.3390/catal14080509 - 7 Aug 2024
Viewed by 338
Abstract
This Special Issue of Catalysts is dedicated to recent advances in the research areas of photocatalysts and photocatalyzed reactions [...] Full article
15 pages, 3590 KiB  
Article
Nanocomposite Coatings of Pectin and Oxide Zinc Nanoparticles to Increase Papaya Shelf Life
by Joelma Saures dos Santos, Caroline Cagnin, Bheatriz Silva Morais de Freitas, Richard Marins da Silva, Glaydson Brasileiro Lopes de Jesus, Celso Martins Belisário, Mariana Buranelo Egea, Josemar Gonçalves de Oliveira Filho and Geovana Rocha Plácido
Coatings 2024, 14(8), 990; https://doi.org/10.3390/coatings14080990 - 6 Aug 2024
Viewed by 396
Abstract
Nanocomposite coatings functionalized with antimicrobial nanoparticles could be a promising alternative for the postharvest preservation of fruits. This study aimed to develop nanocomposite coatings based on pectin incorporated with zinc oxide (NPZ) nanoparticles to preserve the postharvest quality of papaya fruits. The coatings [...] Read more.
Nanocomposite coatings functionalized with antimicrobial nanoparticles could be a promising alternative for the postharvest preservation of fruits. This study aimed to develop nanocomposite coatings based on pectin incorporated with zinc oxide (NPZ) nanoparticles to preserve the postharvest quality of papaya fruits. The coatings were prepared using pectin (3%) and NPZ (0%–0.4%). The materials were characterized for water-related properties (water solubility and water vapor permeability) as well as physical, mechanical, morphological, rheological, and structural properties. The coatings were applied to papaya fruits, which were analyzed for weight loss, firmness, titratable acidity, and soluble solids over nine days of storage. Incorporating NPZ (0%–0.4%) did not affect the films’ water solubility and vapor permeability. However, films with NPZ exhibited lower mechanical properties than pure pectin films. Rheological behavior testing indicated that the pectin solution was a Newtonian fluid, whereas pectin solutions with zinc nanoparticles were non-Newtonian fluids. The pectin coating with 0.2% NPZ was the most effective in preserving the postharvest quality of papaya by reducing fruit weight loss and acidity content. Therefore, the developed coatings incorporated with NPZ showed promise for the postharvest preservation of papaya fruits. Full article
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<p>UV-Vis spectroscopy of zinc oxide nanoparticles (NPZs).</p>
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<p>X-ray diffraction of zinc oxide nanoparticles (NPZs).</p>
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<p>Scanning electron microscopy of zinc oxide nanoparticles (NPZs).</p>
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<p>Surface micrographs (1000×) of films consisting of pectin (P), pectin with 0.2% NPZ (P2Z), and pectin with 0.4% NPZ (P4Z).</p>
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<p>FTIR spectra films consisting of pectin (P), pectin with 0.2% NPZ (P2Z), and pectin with 0.4% NPZ (P4Z).</p>
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<p>Relationship between the shear stress and shear rate for pectin (P1), pectin with 0.2% NPZ (P2Z1), pectin with 0.4% NPZ (P4Z1) films at 25 °C (P2), pectin with 0.2% NPZ (P2Z2), and pectin with 0.4% NPZ (P4Z2) films at 40 °C.</p>
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<p>Relationship between apparent viscosity and shear rate for pectin (P1), pectin with 0.2% NPZ (P2Z1), pectin with 0.4% NPZ (P4Z1) films at 25 °C (P2), pectin with 0.2% NPZ (P2Z2), and pectin with 0.4% NPZ (P4Z2) films at 40 °C.</p>
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11 pages, 3808 KiB  
Article
Gold Nanoparticle Mesoporous Carbon Composite as Catalyst for Hydrogen Evolution Reaction
by Erik Biehler, Qui Quach and Tarek M. Abdel-Fattah
Molecules 2024, 29(15), 3707; https://doi.org/10.3390/molecules29153707 - 5 Aug 2024
Viewed by 368
Abstract
Increased environmental pollution and the shortage of the current fossil fuel energy supply has increased the demand for eco-friendly energy sources. Hydrogen energy has become a potential solution due to its availability and green combustion byproduct. Hydrogen feedstock materials like sodium borohydride (NaBH [...] Read more.
Increased environmental pollution and the shortage of the current fossil fuel energy supply has increased the demand for eco-friendly energy sources. Hydrogen energy has become a potential solution due to its availability and green combustion byproduct. Hydrogen feedstock materials like sodium borohydride (NaBH4) are promising sources of hydrogen; however, the rate at which the hydrogen is released during its reaction with water is slow and requires a stable catalyst. In this study, gold nanoparticles were deposited onto mesoporous carbon to form a nano-composite catalyst (AuNP-MCM), which was then characterized via transmission electron microscopy (TEM), powder X-ray diffraction (P-XRD), and scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS). The composite’s catalytic ability in a hydrogen evolution reaction was tested under varying conditions, including NaBH4 concentration, pH, and temperature, and it showed an activation of energy of 30.0 kJ mol−1. It was determined that the optimal reaction conditions include high NaBH4 concentrations, lower pH, and higher temperatures. This catalyst, with its stability and competitively low activation energy, makes it a promising material for hydrogen generation. Full article
(This article belongs to the Special Issue Two-Dimensional Materials: From Synthesis to Applications)
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<p>TEM images of the AuNP-MCM catalyst at scales of (<b>a</b>) 200 nm, (<b>b</b>) 100 nm, (<b>c</b>) 20 nm, and (<b>d</b>) 5 nm.</p>
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<p>SEM/EDX analysis with (<b>a</b>) the SEM micrograph of the AuNP-MCM catalyst at scales of 2 µm and (<b>b</b>) the EDS spectrum correlating to the indicated gold nanoparticle.</p>
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<p>P-XRD spectra for the MCM and AuNP-MCM. The asterisks highlight the location of important peaks.</p>
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<p>Volume of hydrogen generated over time in the hydrogen evolution reactions catalyzed by AuNP-MCM at different NaBH<sub>4</sub> concentrations (793 µmol, 952 µmol, and 1057 µmol).</p>
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<p>Volume of hydrogen generated over time in the hydrogen evolution reactions catalyzed by AuNP-MCM at different pHs (pH 6, pH 7, and pH 8).</p>
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<p>Volume of hydrogen generated over time in the hydrogen evolution reactions catalyzed by AuNP-MCM at different temperatures (273 K, 288 K, 295 K, and 303 K).</p>
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<p>Arrhenius plot for calculating the activation energy of a hydrogen generation reaction with the AuNP-MCM catalyst.</p>
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<p>Testing reusability of the AuNP-MCM catalyst after five consecutive hydrogen generation reactions.</p>
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<p>Proposed mechanism for the hydrolysis of NaBH<sub>4</sub> while catalyzed by AuNP-MCMs.</p>
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25 pages, 4010 KiB  
Review
Nanoclay-Composite Hydrogels for Bone Tissue Engineering
by Hee Sook Hwang and Chung-Sung Lee
Gels 2024, 10(8), 513; https://doi.org/10.3390/gels10080513 - 3 Aug 2024
Viewed by 359
Abstract
Nanoclay-composite hydrogels represent a promising avenue for advancing bone tissue engineering. Traditional hydrogels face challenges in providing mechanical strength, biocompatibility, and bioactivity necessary for successful bone regeneration. The incorporation of nanoclay into hydrogel matrices offers a potential unique solution to these challenges. This [...] Read more.
Nanoclay-composite hydrogels represent a promising avenue for advancing bone tissue engineering. Traditional hydrogels face challenges in providing mechanical strength, biocompatibility, and bioactivity necessary for successful bone regeneration. The incorporation of nanoclay into hydrogel matrices offers a potential unique solution to these challenges. This review provides a comprehensive overview of the fabrication, physico-chemical/biological performance, and applications of nanoclay-composite hydrogels in bone tissue engineering. Various fabrication techniques, including in situ polymerization, physical blending, and 3D printing, are discussed. In vitro and in vivo studies evaluating biocompatibility and bioactivity have demonstrated the potential of these hydrogels for promoting cell adhesion, proliferation, and differentiation. Their applications in bone defect repair, osteochondral tissue engineering and drug delivery are also explored. Despite their potential in bone tissue engineering, nanoclay-composite hydrogels face challenges such as optimal dispersion, scalability, biocompatibility, long-term stability, regulatory approval, and integration with emerging technologies to achieve clinical application. Future research directions need to focus on refining fabrication techniques, enhancing understanding of biological interactions, and advancing towards clinical translation and commercialization. Overall, nanoclay-composite hydrogels offer exciting opportunities for improving bone regeneration strategies. Full article
(This article belongs to the Special Issue Hydrogel-Based Scaffolds with a Focus on Medical Use (2nd Edition))
Show Figures

Figure 1

Figure 1
<p>Properties of hydrogels for bone tissue engineering.</p>
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<p>Considerations and benefits of nanoclay reinforcement in hydrogels for bone tissue engineering.</p>
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<p>Nanoclay-composite hydrogel for 3D printing biomaterial ink. (<b>A</b>) Synthesis process and representative images of a nanoclay sol-like mixture, a nanoclay-methacrylated hyaluronic acid mixture, and a nanoclay-methacrylated hyaluronic acid-alginate gel-like mixture. (<b>B</b>) Representative images of a straight filament and straight filament rotating around the collecting rod. (<b>C</b>) Optical images of straight filaments with diameters of 100, 200, and 300 µm, respectively. (<b>D</b>) Filaments can be formed into spiral shapes to endure extensive stretching, subsequently used to create a handmade clover. (<b>E</b>) 3D printing of complex architectures based on hydrogels. (<b>F</b>) Macroscopic and fluorescence images of the non-porous scaffold and 3D printed porous scaffold based on hydrogels. (<b>G</b>) In vivo micro-CT reconstructed images of calvarial defects at 4 weeks and 8 weeks after implantation. Reproduced with permission from Guo et al. [<a href="#B97-gels-10-00513" class="html-bibr">97</a>].</p>
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<p>Dual nanoengineered DNA hydrogel (DAC) hydrogel for vascularized bone regeneration. (<b>A</b>) Schematic illustration of preparation of DAC hydrogel. (<b>B</b>) Schematics of the extrusion 3D printing process, scale bar: 5 mm. (<b>C</b>) Stability of 3D-printed DAC hydrogels at different pH values. (<b>D</b>) Reaction scheme of QK peptide-conjugated amyloid fibrils (AF-QK). (<b>E</b>) Stimulation effects of various hydrogels on HUVEC migration (<b>Left</b>). Quantitative migration ratio after HUVECs being cultured for 24 h (<b>Right</b>). (<b>F</b>) qRT–PCR analysis of angiogenesis-related gene (VEGF, PDGF-B, CD31, and VWF) expression in HUVECs cultured for 3 days. (<b>G</b>) Mineralized matrix determined by Alizarin red staining for 7 and 14 days. (<b>H</b>) Representative micro-CT images with cross-section and longitudinal section of skull defects implanted with hydrogels. (<b>I</b>) Quantitative analysis of OCN, CD31, and VEGF expression at 4, 8, and 12 weeks. *, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01; ***, <span class="html-italic">p</span> &lt; 0.001. AF = amyloid fibrils, DA = DNA/AF hydrogel, DAC1.0 = DNA/AF/nanoclay hydrogel. Reproduced with permission from Yang et al. [<a href="#B98-gels-10-00513" class="html-bibr">98</a>].</p>
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<p>Gelatin–Sumecton composite hydrogels. (<b>A</b>) Macroscopical images of lyophilized hydrogels. Scale bar = 5 mm. (<b>B</b>) Swelling ratio after 24 h of hydration. Statistical significance: *** <span class="html-italic">p</span> &lt; 0.001. (<b>C</b>) Scanning electron microscopy (SEM) representative images. Scale bar = 200 μm. (<b>D</b>) Compressive stress–strain curves of hydrogels. (<b>E</b>) Histomorphometric analysis showing the percentage of repair among all experimental groups. Same letters displayed in different histograms denote significant differences (<span class="html-italic">p</span> &lt; 0.001) among these groups. (<b>F</b>) Cross-sectional representative images stained with VOF trichrome dye of the defect site. SUM0: gelatin hydrogel without Sumecton, SUM0.5: gelatin–Sumecton composite hydrogel with Sumecton 0.5%, SUM1: gelatin–Sumecton composite hydrogel with Sumecton 1%, SUM2: gelatin–Sumecton composite hydrogel with Sumecton 2%, CT: Connective tissue, DS: Defect site, NB: Newly formed bone. Scale bar is 500 μm in (<b>F</b>). Reproduced with permission from Lukin et al. [<a href="#B114-gels-10-00513" class="html-bibr">114</a>].</p>
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<p>Halloysite nanotube-composite chitosan hydrogels. In vitro biocompatibility of scaffolds: (<b>A</b>) OD values; and (<b>B</b>) live/dead staining of free (control) and encapsulated hASCs in different hydrogels on days 1, 3, and 5 of culture. In vitro osteogenic differentiation of free (control) and encapsulated hASCs in normal medium (NM) and osteogenic medium (OM): (<b>C</b>) ALP activity on days 7 and 14 of culture; and (<b>D</b>) Alizarin red staining on day 21 of culture; scaffolds: (a) CS/GP = chitosan/β-glycerophosphate hydrogel, (b) mHNT2CS/GP = chitosan/β-glycerophosphate hydrogel with chitosan-modified HNTs, and (c) IC@mHNT2CS/GP = chitosan/β-glycerophosphate hydrogel with chitosan-modified HNTs and Icariin. * <span class="html-italic">p</span> &lt; 0.03, ** <span class="html-italic">p</span> &lt; 0.002, *** <span class="html-italic">p</span> &lt; 0.001. Reproduced with permission from Aghdam et al. [<a href="#B119-gels-10-00513" class="html-bibr">119</a>].</p>
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