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21 pages, 1370 KiB  
Article
Thermal, Molecular Dynamics, and Mechanical Properties of Poly(Ethylene Furanoate)/Poly(ε-Caprolactone) Block Copolymers
by Johan Stanley, Panagiotis A. Klonos, Aikaterini Teknetzi, Nikolaos Rekounas, Apostolos Kyritsis, Lidija Fras Zemljič, Dimitra A. Lambropoulou and Dimitrios N. Bikiaris
Molecules 2024, 29(24), 5943; https://doi.org/10.3390/molecules29245943 (registering DOI) - 16 Dec 2024
Abstract
This study presents the synthesis and characterization of a series of multiblock copolymers, poly(ethylene 2,5-furandicarboxylate)-poly(ε-caprolactone) (PEF-PCL), created through a combination of the two-step melt polycondensation method and ring opening polymerization, as sustainable alternatives to fossil-based plastics. The structural confirmation of these block copolymers [...] Read more.
This study presents the synthesis and characterization of a series of multiblock copolymers, poly(ethylene 2,5-furandicarboxylate)-poly(ε-caprolactone) (PEF-PCL), created through a combination of the two-step melt polycondensation method and ring opening polymerization, as sustainable alternatives to fossil-based plastics. The structural confirmation of these block copolymers was achieved through Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy (ATR-FTIR), ensuring the successful integration of PEF and PCL segments. X-ray Photoelectron Spectroscopy (XPS) was employed for chemical bonding and quantitative analysis, providing insights into the distribution and compatibility of the copolymer components. Differential Scanning Calorimetry (DSC) analysis revealed a single glass transition temperature (Tg), indicating the effective plasticizing effect of PCL on PEF, which enhances the flexibility of the copolymers. X-ray Diffraction (XRD) studies highlight the complex relationship between PCL content and crystallization in PEF-PCL block copolymers, emphasizing the need to balance crystallinity and mechanical properties for optimal material performance. Broadband Dielectric Spectroscopy (BDS) confirmed excellent distribution of PEF-PCL without phase separation, which is vital for maintaining consistent material properties. Mechanical properties were evaluated using Nanoindentation testing, demonstrating the potential of these copolymers as flexible packaging materials due to their enhanced mechanical strength and flexibility. The study concludes that PEF-PCL block copolymers are promising candidates for sustainable packaging solutions, combining environmental benefits with desirable material properties. Full article
(This article belongs to the Special Issue Macromolecular Chemistry in Europe)
25 pages, 1843 KiB  
Article
Bimetallic Mesoporous MCM-41 Nanoparticles with Ta/(Ti, V, Co, Nb) with Catalytic and Photocatalytic Properties
by Viorica Parvulescu, Gabriela Petcu, Nicoleta G. Apostol, Irina Atkinson, Simona Petrescu, Adriana Baran, Daniela C. Culita, Ramona Ene, Bogdan Trica and Elena M. Anghel
Nanomaterials 2024, 14(24), 2025; https://doi.org/10.3390/nano14242025 (registering DOI) - 16 Dec 2024
Abstract
Bimetallic (Ta/Ti, V, Co, Nb) mesoporous MCM-41 nanoparticles were obtained by direct synthesis and hydrothermal treatment. The obtained mesoporous materials were characterized by XRD, XRF, N2 adsorption/desorption, SEM, TEM, XPS, Raman, UV-Vis, and PL spectroscopy. A more significant effect was observed on [...] Read more.
Bimetallic (Ta/Ti, V, Co, Nb) mesoporous MCM-41 nanoparticles were obtained by direct synthesis and hydrothermal treatment. The obtained mesoporous materials were characterized by XRD, XRF, N2 adsorption/desorption, SEM, TEM, XPS, Raman, UV-Vis, and PL spectroscopy. A more significant effect was observed on the mesoporous structure, typically for MCM-41, and on optic properties if the second metal (Ti, Co) did not belong to the same Vb group with Ta as V and Nb. The XPS showed for the TaTi-MCM-41 sample that framework titanium is the major component. The new nanoparticles obtained were used as catalysts for oxidation with hydrogen peroxide of olefinic compounds (1,4 cyclohexadiene, cyclohexene, styrene) and photodegradation of organic pollutants (phenol, methyl orange) from water. The results showed improvementsin activity and selectivity in oxidation reactions by the addition of the second metal to the Ta-MCM-41 catalyst. The slow addition of H2O2 was also beneficial for the selectivity of epoxide products and the stability of the catalysts. The band gap energy values decreased in the presence of the second metal, and the band edge diagram evidenced positive potential for all the conduction bands of the bimetallic samples. The highestlevels of photocatalytic degradation were obtained for the samples with TaTi and TaV. Full article
20 pages, 3101 KiB  
Article
Prospection of the Red Biological Patinas Influencing the Urban Scenery Architecture in Portuguese Territory
by Fabio Sitzia, Carla Lisci, Luis Dias, Silvia Macedo Arantes and Ana Teresa Caldeira
Heritage 2024, 7(12), 7236-7255; https://doi.org/10.3390/heritage7120334 (registering DOI) - 16 Dec 2024
Abstract
Portugal’s architecture reflects a rich history influenced by Roman, Moorish, Neoclassical and Romantic styles, with the 20th century marked by Art Deco and colonial influences. Regional styles vary, with white-painted buildings commonly experiencing color changes due to biofilm formation. Visually striking are the [...] Read more.
Portugal’s architecture reflects a rich history influenced by Roman, Moorish, Neoclassical and Romantic styles, with the 20th century marked by Art Deco and colonial influences. Regional styles vary, with white-painted buildings commonly experiencing color changes due to biofilm formation. Visually striking are the red-colored biological patinascommon in the coastal areas. A survey of 120 historical buildings affected by bio-colonization helps to understand the reasons for the patinas’ growing, which beyond natural factors, is often linked to construction defects. A characterization of four samples utilizes Next-Generation Sequencing (NGS) to identify the microorganisms composing the red biofilm, while the SEM-EDS, FTIR-ATR and XRD techniques provide further insights into the biofilm and substrate features. The comprehensive data of biochemical characterization indicate a wide variety of microorganisms, including bacteria and fungi, some of which exhibit potential as producers of a UV-tolerant red/yellow pigment (carotenoid) responsible for the macroscopic coloration of bio-colonization. Full article
11 pages, 2683 KiB  
Article
Increasing SBA-15 Amphoteric Properties by Direct Zr Addition During Synthesis
by Romeo Hernández, José Escobar, José G. Pacheco, José G. Torres, David S. García, Zenaida Guerra, Paz del Ángel, María C. Barrera and Durvel de la Cruz
Catalysts 2024, 14(12), 928; https://doi.org/10.3390/catal14120928 (registering DOI) - 16 Dec 2024
Abstract
Strategies followed to improve SBA-15 surface (essentially inert) included modifications by adding acidic or basic (or both) species during or after silica synthesis. Amphoteric properties are especially important, as some reactions (alcohol dehydration, for instance) require both types of sites to efficiently take [...] Read more.
Strategies followed to improve SBA-15 surface (essentially inert) included modifications by adding acidic or basic (or both) species during or after silica synthesis. Amphoteric properties are especially important, as some reactions (alcohol dehydration, for instance) require both types of sites to efficiently take place. In this work, single Zr (nominal 3, 5, and 10 wt%, as ZrOCl2•8H2O) direct addition during SBA-15 synthesis was used to impart amphoteric characteristics (as determined by NH3 and CO2 TPD) to mesostructured SiO2 matrices. Additional materials characterization included textural (N2 physisorption) and structural (XRD, FTIR, and UV–Vis spectroscopies, and HRTEM as well) studies. Actual solids composition was also determined (EDS). The degree of Zr incorporation into mesoporous silica was enhanced with nominal content in binary formulations, although not necessarily integrated into SBA-15 walls forming Zr-O-Si linkages. It seemed that single ZrO2 domains (framework and extra-framework) could provide suitable amphoteric properties by significantly increasing the number and strength of both acid and basic sites (especially formulations containing nominal 5 wt% Zr), as to those over mesostructured silica matrices. Also, potentially deleterious strong acid sites were avoided. The binary oxides present great potential to be applied in reactions requiring vicinal acid–base pairs (alcohol dehydration, for instance). Full article
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<p>FTIR spectra of pristine SBA-15 and various Zr-modified materials at several nominal contents.</p>
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<p>UV–Vis spectra of pristine SBA-15 and various Zr-modified materials at several nominal contents.</p>
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<p>Micrographs of the SBA-15-based materials prepared. (<b>a</b>) S; (<b>b</b>) Z3S; (<b>c</b>) Z5S; (<b>d</b>) Z10S. Arrows: ZrO<sub>2</sub> amorphous domains.</p>
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<p>NH<sub>3</sub> TPD profiles of various studied materials at different nominal Zr contents.</p>
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<p>CO<sub>2</sub> TPD profiles of various studied materials at different nominal Zr contents.</p>
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<p>Relative ratio (both on a per mass basis) of total acid and basic sites (as determined from NH<sub>3</sub> and CO<sub>2</sub> TPD profiles, respectively) of various studied materials at different nominal Zr contents. SBA-15 (S) as reference.</p>
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<p>Total basic to acid sites (as determined from CO<sub>2</sub> and NH<sub>3</sub> TPD profiles, respectively, both on a per-mass basis) ratio of various studied materials at different nominal Zr contents.</p>
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13 pages, 5496 KiB  
Article
Sustainable Removal of Phenol Dye-Containing Wastewater by Composite Incorporating ZnFe2O4/Nanocellulose Photocatalysts
by Zan Li, Kun Gao, Wenrui Jiang, Jiao Xu and Pavel Lushchyk
Sustainability 2024, 16(24), 11023; https://doi.org/10.3390/su162411023 - 16 Dec 2024
Abstract
The escalating issue of phenol-containing wastewater necessitates the development of efficient and sustainable treatment methods. In this context, we present a novel composite photocatalyst comprising ZnFe2O4 (ZFO) nanoparticles supported on nanocellulose (NC), aimed at addressing this environmental challenge. The synthesis [...] Read more.
The escalating issue of phenol-containing wastewater necessitates the development of efficient and sustainable treatment methods. In this context, we present a novel composite photocatalyst comprising ZnFe2O4 (ZFO) nanoparticles supported on nanocellulose (NC), aimed at addressing this environmental challenge. The synthesis involved a facile hydrothermal method followed by the impregnation of ZFO nanoparticles onto the NC matrix. The morphology and structure of ZFO, NC, and ZFO/NC were investigated by TEM, SEM-EDX, UV–vis, FT-IR, XRD, and XPS analyses. ZFO, as a weakly magnetic semiconductor catalytic material, was utilized in photocatalytic experiments under magnetic field conditions. By controlling the electron spin states through the magnetic field, electron–hole recombination was suppressed, resulting in improved photocatalytic performance. The results demonstrated that 43% and 76% degradation was achieved after 120 min of irradiation due to ZFO and 0.5ZFO/NC treatment. Furthermore, the composite 0.5ZFO/NC demonstrated the highest photocatalytic efficiency, showing promising recyclability by maintaining its activity after three cycles of use. This study underscores the potential of the ZFO/NC composite for sustainable wastewater treatment, offering a promising avenue for environmental remediation. Full article
(This article belongs to the Special Issue Advanced Materials and Processes for Wastewater Treatment)
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<p>XRD patterns of NC, ZFO, and hybrid nanocomposites.</p>
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<p>FT-IR spectra of NC, ZFO, and ZFO/NC nanocomposites.</p>
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<p>(<b>a</b>) UV–visible spectra and (<b>b</b>) Tauc plots for the band gap of NC, ZFO, and ZFO/NC nanocomposites.</p>
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<p>XPS survey spectra of ZFO and ZFO/NC: (<b>a</b>) Fe 2p, (<b>b</b>) Zn 2p, (<b>c</b>) O 1s, (<b>d</b>) C 1s.</p>
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<p>Characterization of synthesized NC and nanocomposites. (<b>a</b>,<b>b</b>) denote TEM images for NC and ZFO/NC, respectively. (<b>c</b>,<b>d</b>) denote SEM images for NC and ZFO/NC, respectively.</p>
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<p>Elemental compositions of (<b>a</b>) ZFO and NC and (<b>b</b>) hybrid nanocomposites; (<b>c</b>) EDS mapping results for ZFO.</p>
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<p>(<b>a</b>) Degradation curves of phenol by NC, ZFO, and xZFO/NC (x = 0.1, 0.3, 0.5, and 0.7) in the absence of a magnetic field; (<b>b</b>) degradation curves of phenol by NC, ZFO, and xZFO/NC under magnetic field conditions; (<b>c</b>) comparison of the degradation efficiency of xZFO/NC in the absence of a magnetic field and in the presence of a magnetic field; (<b>d</b>) the percentage increase in the photodegradation rate of xZFO/NC after the addition of a magnetic field.</p>
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<p>(<b>a</b>) UV–visible absorption spectra of phenol and phenol under UV–vis; (<b>b</b>) absorption spectra of the degradation of phenol by 0.5ZFO/NC under the condition of a magnetic field as a function of time.</p>
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<p>Cyclic experiments on photocatalytic degradation of phenol by 0.5ZFO/NC.</p>
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<p>0.5ZFO/NC in the absence of a magnetic field and in the presence of a magnetic field (MF = magnetic field; NMF = no magnetic field): (<b>a</b>) photocurrent response density; (<b>b</b>) electrochemical impedance spectroscopy (CPE = Constant Phase Angle Element).</p>
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<p>Schematic of the mechanism of visible-light photocatalytic phenol degradation by NC, ZFO, and xZFO/NC.</p>
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16 pages, 3071 KiB  
Article
Effect of Calcination-Induced Oxidation on the Photocatalytic H2 Production Performance of Cubic Cu2O/CuO Composite Photocatalysts
by Chi-Jung Chang, Chun-Wen Kang and Arul Pundi
Catalysts 2024, 14(12), 926; https://doi.org/10.3390/catal14120926 (registering DOI) - 16 Dec 2024
Viewed by 78
Abstract
This study explores the H2 production performance of CuO/Cu2O with different morphology (nanocubes) synthesized by different methods using different sacrificial reagent (lactic acid), compared with the other three reported CuO/Cu2O photocatalysts used for H2 production. A cubic [...] Read more.
This study explores the H2 production performance of CuO/Cu2O with different morphology (nanocubes) synthesized by different methods using different sacrificial reagent (lactic acid), compared with the other three reported CuO/Cu2O photocatalysts used for H2 production. A cubic Cu2O photocatalyst was prepared using a hydrothermal method. It was then calcined at a certain temperature to form a cubic Cu2O/CuO composite photocatalyst. XRD, TEM, and XPS spectra confirmed the successful synthesis of cubic Cu2O/CuO composite photocatalysts by calcination-induced oxidation at a certain temperature. As the calcination temperature increases, the crystal phase of the photocatalyst changes from Cu2O to Cu2O/CuO and then to CuO. The effects of calcination-induced oxidation on morphology, light absorption, the separation of photoexcited carriers, and the H2 production activity of photocatalysts were studied. EPR spectra were monitored to analyze the oxygen vacancies in different samples. Mott–Schottky and Tauc plots were utilized to establish the band structure of the composite photocatalyst. Cu2O/CuO is a type II photocatalyst with a heterogeneous structure that helps to improve electron–hole separation efficiency. The H2 production efficiency of Cu2O/CuO composite photocatalyst reaches 11,888 μmol h−1g−1, 1.6 times that of Cu2O. The formation of the Cu2O/CuO heterojunction leads to enhanced light absorption, charge separation, and hydrogen production activity. Full article
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Figure 1
<p>XRD spectra of (i) Cu<sub>n</sub>O, (ii) Cu<sub>n</sub>O-275, (iii) Cu<sub>n</sub>O-300, (iv) Cu<sub>n</sub>O-350, (v) Cu<sub>n</sub>O-400, and (vi) Cu<sub>n</sub>O-500 samples.</p>
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<p>FESEM images of (<b>a</b>) Cu<sub>n</sub>O, (<b>b</b>) Cu<sub>n</sub>O-300, (<b>c</b>) Cu<sub>n</sub>O-500; and the (<b>d</b>) TEM, (<b>e</b>) HR-TEM, and (<b>f</b>) SAED of Cu<sub>n</sub>O-300 photocatalyst.</p>
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<p>EDX of (<b>a</b>) edges and (<b>b</b>) center areas of the Cu<sub>n</sub>O-300 photocatalyst.</p>
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<p>XPS (<b>a</b>) Cu2p and (<b>b</b>) O1s spectra of Cu<sub>n</sub>O; XPS (<b>c</b>) Cu2p and (<b>d</b>) O1s spectra of Cu<sub>n</sub>O-30; and XPS (<b>e</b>) Cu2p and (<b>f</b>) O1s spectra of Cu<sub>n</sub>O-500.</p>
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<p>(<b>a</b>) DRS (<b>b</b>) Tauc plots of (i) Cu<sub>n</sub>O, (ii) Cu<sub>n</sub>O-300, (iii) Cu<sub>n</sub>O-500; (<b>c</b>) photocatalytic hydrogen production activity of uncalcined Cu<sub>n</sub>O, and Cu<sub>n</sub>O-200, Cu<sub>n</sub>O-300, Cu<sub>n</sub>O-400, Cu<sub>n</sub>O -500 photocatalysts calcined at different temperatures (200, 300, 400, and 500 °C). (<b>d</b>) EIS and (<b>e</b>) photocurrent–time curves under the light on/off illumination by the Xe lamp. (<b>f</b>) PL spectra of (i) Cu<sub>n</sub>O, (ii) Cu<sub>n</sub>O-300, and (iii) Cu<sub>n</sub>O-500 samples.</p>
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<p>Mott–Schottky plots for (<b>a</b>) Cu<sub>2</sub>O and (<b>b</b>) CuO; (<b>c</b>) band structure of Cu<sub>2</sub>O and CuO; and (<b>d</b>) EPR spectra of Cu<sub>n</sub>O, Cu<sub>n</sub>O-300, and Cu<sub>n</sub>O-500 samples.</p>
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13 pages, 4203 KiB  
Article
Porous Carbon Fabricated by Microbial Pretreatment of Brewer’s Grain for the Improvement of Toluene Adsorption Performance
by Jingxin Wang, Xiaohong Wang, Xiaoping Lin, Ziyi Yu, Davide Vione, Haomin Huang, Xiaohong Zhang, Yanhong Zhang, Jiaqi He, Yun Xia and Hansun Fang
Molecules 2024, 29(24), 5931; https://doi.org/10.3390/molecules29245931 (registering DOI) - 16 Dec 2024
Viewed by 50
Abstract
Porous activated carbons (AC-AN and AC-AO) for toluene adsorption were prepared starting from brewer’s grain biomass pretreated with microorganisms (Aspergillus niger van Tieghem for AC-AN and Aspergillus oryzae RIB40 for AC-AO). The structures and chemical properties of the three activated carbon materials [...] Read more.
Porous activated carbons (AC-AN and AC-AO) for toluene adsorption were prepared starting from brewer’s grain biomass pretreated with microorganisms (Aspergillus niger van Tieghem for AC-AN and Aspergillus oryzae RIB40 for AC-AO). The structures and chemical properties of the three activated carbon materials (AC-AN, AC-AO, and AC that was not pretreated with microorganisms) were characterized by N2 adsorption–desorption isotherms, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The adsorption behavior of the three activated carbons for toluene was studied and correlated with the physical and chemical properties of these materials. The results suggested that the activated carbons prepared by microbial pretreatment had a rougher morphology, higher specific surface area, richer pore structure, fewer oxygen-containing functional groups on the surface, and better adsorption performance for toluene (increased by 31.5% and 18.3% with AC-AN and AC-AO, respectively) compared with the untreated activated carbon (AC). The Thomas model was used to fit the toluene adsorption data, indicating that the rich pore structure accelerated the kinetic process of toluene adsorption. Therefore, appropriate microbial pretreatment of the feedstock that is used to prepare activated carbon can effectively improve its adsorption capacity towards toluene. Full article
(This article belongs to the Section Materials Chemistry)
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Graphical abstract

Graphical abstract
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<p>The morphology and structure of the ACs (AC (<b>a</b>,<b>d</b>), AC-AN (<b>b</b>,<b>e</b>), and AC-AO (<b>c</b>,<b>f</b>)) as studied by both SEM (<b>a</b>–<b>c</b>) and TEM (<b>d</b>–<b>f</b>).</p>
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<p>(<b>a</b>) The N2 adsorption–desorption isotherms and (<b>b</b>) pore-size distributions (PSDs) of ACs.</p>
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<p>FTIR spectra of the investigated ACs.</p>
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<p>Raman spectra of ACs.</p>
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<p>X-ray diffraction (XRD) spectra of ACs.</p>
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<p>Curve-fitted C1s (<b>a</b>) and O1s (<b>b</b>) of XPS spectra for ACs.</p>
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<p>Breakthrough curves (<b>a</b>), the relationship of SBET and adsorption capacities (<b>b</b>), and the Thomas model (<b>c</b>) of ACs.</p>
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14 pages, 5260 KiB  
Article
Thermal Stability of Residual Stress, Microstructure, and Mechanical Property in Shot-Peened CNT/Al-Cu-Mg Composites
by Wenlong Zhu, Shilong Xing, Lianbo Wang, Zhaoyang Yang, Wenliang Yu, Ang Yin, Wenbo Li, Chuanhai Jiang and Vincent Ji
Coatings 2024, 14(12), 1571; https://doi.org/10.3390/coatings14121571 - 16 Dec 2024
Viewed by 143
Abstract
To investigate the thermal stability of a shot-peened specimen and ensure the reliability operation under high temperatures, CNT/Al-Cu-Mg composites were treated by shot peening (SP) and the isothermal aging treatment. The heating temperatures were 100, 150, 200, and 250 °C. Changes in surface [...] Read more.
To investigate the thermal stability of a shot-peened specimen and ensure the reliability operation under high temperatures, CNT/Al-Cu-Mg composites were treated by shot peening (SP) and the isothermal aging treatment. The heating temperatures were 100, 150, 200, and 250 °C. Changes in surface residual stress and the distribution along the depth were investigated. The microstructure changes were analyzed by XRD and observed by TEM. Changes in mechanical properties were characterized by microhardness. The results show that the compressive residual stress (CRS) release and the microstructure changes mainly occurred at the initial stage of heating treatment. After 128 min of isothermal aging treatment at 250 °C, the surface CRS released 91.9% and the maximum CRS released 80.9%, the surface domain size increased by 222%, and the microstrain and microhardness decreased by 49% and 27.3%, respectively. The reinforcement effect introduced by SP basically disappeared. A large number of second-phase particles, such as CNT, Al2Cu, and Al4C3, were anchored at grain boundaries, hindering dislocation movement and enhancing the thermal stability of the material. Isothermal aging treatment at 100 °C and 150 °C for a duration of 32 min is a reliable circumstance for maintaining SP reinforcement. Full article
(This article belongs to the Special Issue Latest Insights in Metal Fatigue, Failure, and Fracture)
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Figure 1
<p>The CNT/Al-Cu-Mg composites: (<b>a</b>) XRD, (<b>b</b>) microstructure.</p>
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<p>Changes in residual stress during continuous heating test.</p>
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<p>Changes in residual stress during the isothermal aging treatment.</p>
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<p>Linear relationship diagram between <math display="inline"><semantics> <mrow> <mi mathvariant="normal">l</mi> <mi mathvariant="normal">o</mi> <mi mathvariant="normal">g</mi> <mfenced separators="|"> <mrow> <mo>−</mo> <mi mathvariant="normal">l</mi> <mi mathvariant="normal">n</mi> <mstyle scriptlevel="0" displaystyle="true"> <mfrac> <mrow> <msubsup> <mrow> <mi mathvariant="sans-serif">σ</mi> </mrow> <mrow> <mi mathvariant="normal">T</mi> </mrow> <mrow> <mi mathvariant="normal">R</mi> <mi mathvariant="normal">S</mi> </mrow> </msubsup> </mrow> <mrow> <msubsup> <mrow> <mi mathvariant="sans-serif">σ</mi> </mrow> <mrow> <mn>0</mn> </mrow> <mrow> <mi mathvariant="normal">R</mi> <mi mathvariant="normal">S</mi> </mrow> </msubsup> </mrow> </mfrac> </mstyle> </mrow> </mfenced> </mrow> </semantics></math> and log t. The slope represents the m values.</p>
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<p>Linear relationship diagram between log t and 1/kT. T is the temperature at which CRS is released halfway. The slope represents the <math display="inline"><semantics> <mrow> <msub> <mrow> <mo>∆</mo> <mi mathvariant="normal">H</mi> </mrow> <mrow> <mi mathvariant="sans-serif">σ</mi> </mrow> </msub> </mrow> </semantics></math>/ln10 values.</p>
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<p>Changes in CRS along the depth direction after the isothermal aging treatment.</p>
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<p>XRD maps of the initial state after SP and after 250 °C isothermal aging.</p>
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<p>Changes in FWHM of the Al (111) diffraction peak along the depth direction.</p>
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<p>Changes in the domain size and the microstrain under different annealing times: (<b>a</b>) domain size, (<b>b</b>) microstrain.</p>
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<p>The TEM of the samples at initial state and after SP: (<b>a</b>) at initial state, (<b>b</b>) mapping of the corresponding area (<b>c</b>,<b>d</b>) after SP.</p>
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<p>The diagram of the subgrain coalescence and the TEM after 250 °C isothermal aging treatment: (<b>a</b>) diagram, (<b>b</b>,<b>c</b>) TEM.</p>
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<p>The surface hardness distributions before and after 250 °C isothermal aging treatment. (<b>a</b>) before the isothermal aging treatment and (<b>b</b>)after the isothermal aging treatment.</p>
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<p>The hardness distributions along the depth before and after the isothermal aging treatment.</p>
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13 pages, 3241 KiB  
Article
Isolating and Identifying One Strain with Lead-Tolerant Fungus and Preliminary Study on Its Capability of Biosorption to Pb2+
by Wanna Li, Liujing Zhao, Cui Liu, Xingpeng Bai, Chenyuan Xu, Fengqiu An and Feilong Sun
Biology 2024, 13(12), 1053; https://doi.org/10.3390/biology13121053 - 16 Dec 2024
Viewed by 168
Abstract
To obtain lead-resistant microorganisms as potential strains for bioremediation, in this study, a strain of fungus with high resistance to lead was isolated and domesticated from lead-contaminated soil, which was cultured and molecularly biologically identified as the genus Sarocladium Pb-9 (GenBank No. MK372219). [...] Read more.
To obtain lead-resistant microorganisms as potential strains for bioremediation, in this study, a strain of fungus with high resistance to lead was isolated and domesticated from lead-contaminated soil, which was cultured and molecularly biologically identified as the genus Sarocladium Pb-9 (GenBank No. MK372219). The optimal incubation time of strain Pb-9 was 96 h, the optimal incubation temperature was 25 °C, and the optimal incubation pH was 7. The strain Pb-9 had a good adsorption effect on Pb2+ at a lead concentration of 2000 mg/L; scanning electron microscopy (SEM) observed that the spores of the Pb-9 strain appeared to be wrinkled and deformed under Pb2+ stress, and XRD analysis showed that the mycelium of Pb-9 adsorbed Pb2+; Fourier transform infrared spectroscopy (FTIR) analysis showed that the Pb-9 strain might produce substances such as esters and polysaccharides under the treatment of different Pb2+ concentrations. The above results showed that strain Pb-9 has good resistance and adsorption capacity to lead. Therefore, it has potential application value in the bioremediation of environmental heavy metal pollution, and this study provides a fundamental basis for the bioremediation of lead pollution in the environment. Full article
(This article belongs to the Section Toxicology)
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<p>Colony morphology, the microstructure of mycelia, and spores of strain Pb-9 (25 °C, 5 d). Note: (<b>A</b>): Pb-9 strain; (<b>B</b>): Mycelia and spores (1000×; where the eyepiece is 10×).</p>
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<p>Phylogenetic tree of strains Pb-9.</p>
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<p>Growth curves of strain Pb-9.</p>
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<p>Effect of temperature (<b>A</b>) and pH (<b>B</b>) on the growth of strain Pb-9. Note: The standard error takes into account the error of the scale.</p>
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<p>Adsorption rate of Pb<sup>2+</sup> by strain Pb-9 at different Pb<sup>2+</sup> concentrations.</p>
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<p>SEM micrographs of strain Pb-9 treated with different concentrations of Pb<sup>2+</sup>. Note: microstructure of mycelia: (<b>A</b>): CK; (<b>B</b>): 3000 mg/kg; microstructure of spores (<b>C</b>): CK; (<b>D</b>): 2000 mg/kg; (<b>E</b>): 3000 mg/kg; (<b>F</b>): 4000 mg/kg; (<b>A</b>) magnification times 3000×; (<b>B</b>) magnification times 5500×; (<b>C</b>,<b>D</b>) magnification times 5000×; (<b>E</b>) magnification times 20,000×; (<b>F</b>) magnification times 10,000×.</p>
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<p>X-ray diffractogram of strain Pb-9 treated with different concentrations of Pb<sup>2+</sup>.</p>
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<p>Infrared analysis of strain Pb-9 treated with different concentrations of Pd<sup>2+</sup>.</p>
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12 pages, 12558 KiB  
Article
The Effects of Surface Plasma Carburization on the Microstructure and Molten Salt Corrosion Resistance of Ta
by Xuming Lv, Dongbo Wei, Xianpu Huang, Zeyu Gao and Pingze Zhang
Coatings 2024, 14(12), 1570; https://doi.org/10.3390/coatings14121570 - 16 Dec 2024
Viewed by 189
Abstract
In order to enhance the corrosion resistance of tantalum, the double-glow plasma (DGP) metallurgy technique was used to prepare TaC coatings on the tantalum. The morphology, microstructure, and phase constituents of TaC were examined by scanning electron microscopy (SEM) and X-ray diffraction (XRD). [...] Read more.
In order to enhance the corrosion resistance of tantalum, the double-glow plasma (DGP) metallurgy technique was used to prepare TaC coatings on the tantalum. The morphology, microstructure, and phase constituents of TaC were examined by scanning electron microscopy (SEM) and X-ray diffraction (XRD). Nano-indentation tests were used to evaluate the mechanical properties of the coatings. The specimens were immersed in NaCl-KCl molten salt at 830 °C to evaluate their corrosion resistance. The results showed that the coating prepared by the DGP technique has a thickness of approximately 5 µm, the diffusion layer has a thickness of 2.5 µm, and the nano-indentation hardness is measured to be 17.27 GPa. The high-temperature stable ceramic phase enhances the high-temperature oxidation resistance of pure tantalum (Ta), while the dense corroded surface and oxidation products improve the anti-corrosion property of TaC coatings. Full article
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<p>Schematic illustration of double-glow plasma surface carburizing technology producing TaC coatings on Ta surface.</p>
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<p>Surface SEM (<b>a</b>) and cross-section SEM (<b>c</b>) and XRD (<b>b</b>), EDS (<b>d</b>) analysis of carburization layer.</p>
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<p>Mechanical properties of the Ta matrix and TaC carburized coating layer. (<b>a</b>) Load-displacement curves; (<b>b</b>) nano-hardness and elastic modulus; (<b>c</b>) H/E and H<sup>3</sup>/E<sup>2</sup> ratios; (<b>d</b>) elastic work (W<sub>e</sub>), plastic work (W<sub>p</sub>), and their ratio (K).</p>
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<p>XRD pattern of Ta (<b>a</b>) and TaC (<b>b</b>) coatings after molten salt corrosion.</p>
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<p>Corrosion kinetics of TaC coatings and untreated Ta in NaCl-KCl melts.</p>
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<p>Surface morphologies of the Ta and TaC infiltration layers after molten salt corrosion. (<b>a</b>–<b>a2</b>) Ta 1 h, 4 h, 7 h; (<b>b</b>–<b>b2</b>) TaC 1 h, 4 h, 7 h.</p>
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<p>Cross-sectional morphology and elemental line scan of Ta matrix after molten salt corrosion for (<b>a</b>,<b>a1</b>) 1 h, (<b>b</b>,<b>b1</b>) 4 h, and (<b>c</b>,<b>c1</b>) 7 h, respectively. Cross-sectional morphology and elemental line scan of TaC infiltration layer after molten salt corrosion for (<b>d</b>,<b>d1</b>) 1 h, (<b>e</b>,<b>e1</b>) 4 h, and (<b>f</b>,<b>f1</b>) 7 h, respectively.</p>
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<p>Schematic illustration of corrosion behaviors of Ta and TaC coatings in NaCl-KCl molten salt.</p>
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13 pages, 3858 KiB  
Article
The Controlling Effect of CaCO3 Supersaturation over Zn Carbonate Assemblages: Co-Crystallization in Silica Hydrogel
by André Jorge Pinto, Nuria Sánchez-Pastor and Angeles Fernández-González
Minerals 2024, 14(12), 1274; https://doi.org/10.3390/min14121274 - 15 Dec 2024
Viewed by 466
Abstract
Weathering products of sphalerite-bearing ores play an important role in controlling the fate of Zn in the environment. In this framework, the relative stability of Zn carbonates is of special relevance for the common case of ore weathering by carbonated groundwater in the [...] Read more.
Weathering products of sphalerite-bearing ores play an important role in controlling the fate of Zn in the environment. In this framework, the relative stability of Zn carbonates is of special relevance for the common case of ore weathering by carbonated groundwater in the presence of calcium carbonates. We investigated the experimental (co)nucleation and growth of Zn and Ca carbonates at 25 °C in finite double diffusion silica hydrogel media with the purpose of deciphering the system’s reactive pathway and unraveling the major governing factors behind the obtained mineral assemblages. The crystallized solids were carefully extracted two months post-nucleation and studied with micro-Raman spectroscopy, micro X-ray diffraction (XRD), scanning electron microscopy, and electron microprobe (EMP) methods. The obtained results indicate that the grown Zn-bearing phases corresponded to smithsonite and/or Zn hydroxyl carbonate, while CaCO3 polymorphs aragonite and calcite were also crystallized. Moreover, the observed mineral textural relationships reflected the interplay between supersaturation with respect to CaCO3/pCO2 and the grown Zn-bearing carbonate. Experiments conducted in more supersaturated conditions with respect to CaCO3 polymorphs (higher pCO2) favored the precipitation of smithsonite, while the opposite was true for the obtained Zn hydroxyl carbonate phase. The gathered Raman, XRD, and EMP data indicate that the latter phase corresponded to a non-stoichiometric, poorly crystalline solid. Full article
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Graphical abstract

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<p>Experimental setup used for crystal growth.</p>
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<p>Representative Raman spectra of solids obtained in experiments 1 and 2, relative to the shift intervals (<b>a</b>) 50 &lt; cm<sup>−1</sup> &lt; 450 and (<b>b</b>) 990 &lt; cm<sup>−1</sup> &lt; 1140. The inset in (<b>a</b>) depicts a BSE micrograph of a grown solid polished section, with the corresponding Zn% compositional profile measured with EMP. Hznc = Hydrozincite; Prds = Parádsasvárite; Vtr = Vaterite; Smt = Smithsonite.</p>
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<p>Representative micro-X-ray diffraction pattern obtained in a solid grown in experiments 1 and 2. The * marks reflections assignable to parádsasvárite [<a href="#B22-minerals-14-01274" class="html-bibr">22</a>]. Negative intensity values are an artifact of background noise removal, without which, pattern interpretation was not possible.</p>
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<p>BSE micrographs of solids grown in experiment 3. (<b>a</b>) Calcite (Cal) crystal displaying a hopper-like growth pattern. The inset displays a polished section of a rosette aggregate of aragonite (Arg) crystals. (<b>b</b>) Zn hydroxyl carbonate spherules (Zn OH-Carb), as obtained in experiments 1 and 2, calcite, and a multi-phase spherule (*) whose Raman spectral analysis revealed a core of Zn hydroxyl carbonate overgrown by layers of smithsonite.</p>
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<p>(<b>a</b>) Polarized reflected-light micrograph of a cross-sectioned multi-phase spherule obtained in experiment 3. The Raman spectra of each grown morphology (I, II, and III) are displayed in (<b>b</b>,<b>c</b>). Smt = smithsonite, Hznc = hydrozincite, Prds = parádsasvárite. * Bands not assigned to smithsonite, see text for explanation.</p>
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<p>BSE micrographs of representative solids grown in experiments 4–9: (<b>a</b>) aragonite (Arg); (<b>b</b>) calcite (Cal) and aragonite with an overgrowth; (<b>c</b>) calcite with an overgrowth; and (<b>d</b>) Zn hydroxyl carbonate.</p>
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<p>(<b>a</b>) BSE micrograph of a cross-sectioned overgrown calcite crystal, representative of those grown in experiments 4–9. The Raman spectra of each grown phase (I and II) are displayed in (<b>b</b>) and (<b>c</b>). Hznc = hydrozincite. * Bands not assigned to smithsonite, see text for explanation.</p>
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<p>(<b>a</b>) BSE micrograph of a cross-sectioned overgrown aragonite crystal, representative of those grown in experiments 10–15. The Raman spectra of each grown phase (I and II) are displayed in (<b>b</b>,<b>c</b>). The spectrum of smithsonite obtained in experiments at higher supersaturation with respect to Zn carbonates (<a href="#minerals-14-01274-f007" class="html-fig">Figure 7</a>c) is displayed in (<b>c</b>). * Bands not assigned to aragonite or smithsonite, see text for explanation.</p>
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<p>Schematic growth sequence of the multi-phase spherule analyzed in <a href="#minerals-14-01274-f005" class="html-fig">Figure 5</a>a. See text for explanation. Smt = smithsonite, Cal = calcite, Zn OH-Carb = zinc hydroxyl carbonate, Sat<sub>phase</sub> = thermodynamic saturation with respect to the phase in subscript.</p>
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19 pages, 25398 KiB  
Article
Red Mud in Combination with Construction Waste Red Bricks for the Preparation of Low-Carbon Binder Materials: Design and Material Characterization
by Teng Qin, Hui Luo, Rubin Han, Yunrui Zhao, Limin Chen, Meng Liu, Zhihang Gui, Jiayao Xing, Dongshun Chen and Bao-Jie He
Buildings 2024, 14(12), 3982; https://doi.org/10.3390/buildings14123982 - 15 Dec 2024
Viewed by 386
Abstract
The effective and safe treatment of red mud has become a pressing global issue in recent years. The purpose of this study is to prepare different systems of low-carbon cementitious materials by combining various solid wastes (slag powder, red brick of construction waste) [...] Read more.
The effective and safe treatment of red mud has become a pressing global issue in recent years. The purpose of this study is to prepare different systems of low-carbon cementitious materials by combining various solid wastes (slag powder, red brick of construction waste) with different systems of low-carbon cementitious materials and to observe the effects of different cementitious compositions on the construction performance, mechanical properties, freeze–thaw resistance, and heavy metal leaching properties by designing different systems of low-carbon cementitious materials, as well as to analyze the microscopic morphology, mineral composition, and strength-forming mechanisms of the different systems of low-carbon cementitious materials through the use of X-ray fluorescence (XRF), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) techniques. The findings reveal that a ternary cementitious system containing 16% red brick powder exhibits the most favorable overall performance. Compared to a binary system, this mixture improves fluidity by 4.5%, increases compressive strength by 18.27%, reduces drying shrinkage by 39.56%, and lowers the mass loss rate during dry–wet cycling by 11.07%. Furthermore, the leaching levels of heavy metals such as Cr, As, Pb, Ni, and Cu in the red mud-based cementitious materials, combined with multiple solid wastes, are within the safe limits for non-hazardous environmental release, as specified by Chinese regulations, under both freeze–thaw and non-freeze–thaw conditions. This study demonstrates for the first time the potential of combining red mud with construction waste brick dust and provides a scientific basis and theoretical guidance for the synergistic utilization of alkaline solid waste, calcium solid waste, and silica–aluminum solid waste. Full article
(This article belongs to the Section Building Materials, and Repair & Renovation)
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<p>XRD, particle size distribution, and SEM images of raw materials: (<b>a</b>,<b>d</b>,<b>g</b>) RM, (<b>b</b>,<b>e</b>,<b>h</b>) RB, (<b>c</b>,<b>f</b>,<b>i</b>) MP.</p>
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<p>A flowchart of the preparation of low-carbon gelling materials.</p>
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<p>Flowability of low-carbon gelling material: (<b>a</b>) binary system; (<b>b</b>) ternary system.</p>
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<p>Mechanical properties of low-carbon gelling material: (<b>a</b>) binary system; (<b>b</b>) ternary system.</p>
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<p>Drying shrinkage and mass loss of low-carbon gelling material. (<b>a</b>) Drying shrinkage of binary gelling material; (<b>b</b>) mass loss rate of binary gelling material; (<b>c</b>) drying shrinkage of ternary gelling material; (<b>d</b>) mass loss rate of ternary gelling material.</p>
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<p>The mass loss and rate of loss for binary and ternary gelling materials during wet and dry cycling.</p>
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<p>Microanalysis of low-carbon cementitious materials: (<b>a</b>–<b>e</b>) SEM images of binary and ternary cementitious materials at different magnifications; (<b>f</b>–<b>j</b>) EDS images of binary and ternary cementitious materials showing the distribution of different elements.</p>
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<p>Microscopic analysis of low-carbon gelling material: (<b>a</b>–<b>e</b>) XRD patterns and FTIR spectra.</p>
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<p>Frost resistance of low-carbon gelling material: (<b>a</b>) binary system; (<b>b</b>) ternary system.</p>
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<p>Heavy metal leaching characteristics of low-carbon cementitious materials: (<b>a</b>) freeze–thaw; (<b>b</b>) non-freeze–thaw.</p>
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23 pages, 4064 KiB  
Article
Investigation of the Photocatalytic Activity of Copper-Modified Commercial Titania (P25) in the Process of Carbon Dioxide Photoreduction
by Konrad Sebastian Sobczuk, Iwona Pełech, Daniel Sibera, Piotr Staciwa, Agnieszka Wanag, Ewa Ekiert, Joanna Kapica-Kozar, Katarzyna Ćmielewska, Ewelina Kusiak-Nejman, Antoni Waldemar Morawski and Urszula Narkiewicz
Materials 2024, 17(24), 6139; https://doi.org/10.3390/ma17246139 (registering DOI) - 15 Dec 2024
Viewed by 302
Abstract
Abstract: The photocatalytic reduction of CO2 to useful products is an area of active research because it shows a potential to be an efficient tool for mitigating climate change. This work investigated the modification of titania with copper(II) nitrate and its [...] Read more.
Abstract: The photocatalytic reduction of CO2 to useful products is an area of active research because it shows a potential to be an efficient tool for mitigating climate change. This work investigated the modification of titania with copper(II) nitrate and its impact on improving the CO2 reduction efficiency in a gas-phase batch photoreactor under UV–Vis irradiation. The investigated photocatalysts were prepared by treating P25-copper(II) nitrate suspensions (with various Cu2+ concentrations), alkalized with ammonia water, in a microwave-assisted solvothermal reactor. The titania-based photocatalysts were characterized by SEM, EDS, ICP-OES, XRD and UV-Vis/DR methods. Textural properties were measured by the low-temperature nitrogen adsorption/desorption studies at 77 K. P25 photocatalysts modified with copper(II) nitrate used in the process of carbon dioxide reduction allowed for a higher efficiency both for the photocatalytic reduction of CO2 to CH4 and for the photocatalytic water decomposition to hydrogen as compared to a reference. Similarly, modified samples showed significantly higher selectivity towards methane in the CO2 conversion process than the unmodified sample (a change from 30% for a reference sample to 82% for the P25-R-Cu-0.1 sample after the 6 h process). It was found that smaller loadings of Cu are more beneficial for increasing the photocatalytic activity of a sample. Full article
(This article belongs to the Special Issue Advances in Photocatalyst Materials and Green Chemistry)
11 pages, 4025 KiB  
Article
Experimental Research on Permeability and Effective Radon Reduction of Chemical Solidification of Uranium Tailings
by Jindong Wang and Shuai Zhang
Atmosphere 2024, 15(12), 1493; https://doi.org/10.3390/atmos15121493 - 14 Dec 2024
Viewed by 425
Abstract
To be able to study the permeability coefficient and radon reduction effect of three materials before and after the solidification of uranium tailings. Firstly, uranium tailings, blast furnace slag, lime, fly ash and cement were selected as raw materials for the experiment. Three [...] Read more.
To be able to study the permeability coefficient and radon reduction effect of three materials before and after the solidification of uranium tailings. Firstly, uranium tailings, blast furnace slag, lime, fly ash and cement were selected as raw materials for the experiment. Three solidified materials were mixed with 7.5%, 10% and 12.5% of equal proportions of cement. The curing samples of nine kinds of solidified bodies were prepared after curing. Subsequently, the permeability coefficient was determined through the utilization of X-ray diffraction (XRD) and scanning electron microscopy (SEM). And cumulative radon concentrations in uranium tailings and samples were measured by RAD7. Thus, the radon exhalation rate of the original sample and the sample were determined. The experimental results show that the permeability coefficient of nine samples decreased with the quadratic function with the increase in the amount of curing agent. Microscopic scanning results show that there is a positive correlation among the radon exhalation rate, permeability coefficient and cementation degree. The best material for solidifying uranium tailings and radon insulation was blast furnace slag, followed by fly ash. Full article
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<p>XRD patterns of fly ash samples.</p>
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<p>SEM images of uranium tailing sample.</p>
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<p>Scanning electron microscopy results of uranium tailings and samples mixed with different curing agents.</p>
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<p>The permeability coefficient curve of each sample.</p>
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<p>Uranium tailings and single-sided radon exhalation rate curve of each sample.</p>
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<p>Relationship between permeability coefficient and radon exhalation rate of each sample.</p>
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31 pages, 10953 KiB  
Article
Immobilization of Pb2+, CrO42−, Hg2+, and Cd2+ in Coal Fly Ash/PP-g-MHBP-Based Geopolymers
by Paola M. Fonseca Alfonso, Mercedes Díaz Lagos and Edwin A. Murillo
J. Compos. Sci. 2024, 8(12), 528; https://doi.org/10.3390/jcs8120528 - 14 Dec 2024
Viewed by 494
Abstract
Contamination by heavy metals (HMs) such as Pb, Cd, Cr, and Hg poses significant risks to the environment and human health owing to their toxicity and persistence. Geopolymers (GPs) have emerged as promising materials for immobilizing HMs and reducing their mobility through physical [...] Read more.
Contamination by heavy metals (HMs) such as Pb, Cd, Cr, and Hg poses significant risks to the environment and human health owing to their toxicity and persistence. Geopolymers (GPs) have emerged as promising materials for immobilizing HMs and reducing their mobility through physical encapsulation and chemical stabilization. This study explored the novel use of isotactic polypropylene functionalized in the molten state with maleinized hyperbranched polyol polyester (PP-g-MHBP) as an additive in coal fly ash (CFA)-based GPs to enhance HM immobilization. Various characterization techniques were employed, including compressive strength tests, XRD, ATR-FTIR, SEM-EDX, XPS analyses, and TCLP leaching tests, to assess immobilization effectiveness. These results indicate that although the addition of PP-g-MHBP does not actively contribute to the chemical interactions with HM ions, it acts as an inert filler within the GP matrix. CFA/PP-g-MHBP-based GPs demonstrated significant potential for Cd2+ immobilization up to 3 wt% under acidic conditions, although the retention of Pb2+, CrO42−, and Hg2+ varied according to the specific chemistry of each metal, weight percentage of the added metal, matrix structure, and regulatory standards. Notably, high immobilization percentages were achieved for CrO42− and Hg2+, although the leaching concentrations exceeded US EPA limits. These findings highlight the potential of CFA/PP-g-MHBP-based GPs for environmental applications, emphasizing the importance of optimizing formulations to enhance HM immobilization under varying conditions. Full article
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<p>Schema of the preparation process for the CFA/PP-<span class="html-italic">g</span>-MHBP-based geopolymers.</p>
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<p>Volume and cumulative volume particle size distributions of CFA and PP-<span class="html-italic">g</span>-MHBP samples.</p>
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<p>XRD pattern of the CFA sample with internal standard.</p>
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<p>XRD patterns of (<b>a</b>) the CFA sample and GP1 specimen after 28 days of curing; (<b>b</b>) the GP specimens with 1.0 wt% of Pb<sup>2+</sup>, CrO<sub>4</sub><sup>2−</sup>, Hg<sup>2+</sup>, and Cd<sup>2+</sup> after 28 days of curing; (<b>c</b>) the GP specimens with 3.0 wt% of Pb<sup>2+</sup>, CrO<sub>4</sub><sup>2−</sup>, Hg<sup>2+</sup>, and Cd<sup>2+</sup> after 28 days of curing. The CFA pattern did not include internal standards.</p>
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<p>ATR-FTIR spectra of the CFA sample, the control GP specimen (GP1), and GP specimens containing (<b>a</b>) 1.0 wt% and (<b>b</b>) 3.0 wt% of Pb<sup>2+</sup>, CrO<sub>4</sub><sup>2−</sup>, Cd<sup>2+</sup>, and Hg<sup>2+</sup> after 28 days of curing.</p>
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<p>Effect of HM ion type and content on compressive strength and main transmittance minimum position in the GP specimens.</p>
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<p>SEM images of GPs after 28 days of curing, with 1.0 wt% and 3.0 wt% of (<b>a</b>,<b>b</b>) Pb<sup>2+</sup>, (<b>c</b>,<b>d</b>) CrO<sub>4</sub><sup>2−</sup>, (<b>e</b>,<b>f</b>) Hg<sup>2+</sup>, and (<b>g</b>,<b>h</b>) Cd<sup>2+</sup>, respectively.</p>
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<p>XPS survey spectra of GP1 and GP specimens containing 1 wt% Pb<sup>2+</sup>, Hg<sup>2+</sup>, CrO<sub>4</sub><sup>2−</sup>, and Cd<sup>2+</sup> after 28 days of curing.</p>
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<p>High-resolution XPS spectra of Si 2s, Si 2p, Al 2s, Al 2p, Na 2s, and Pb 4f peaks for the GP1 and GP specimens containing 1 wt% Pb<sup>2+</sup>, Hg<sup>2+</sup>, CrO<sub>4</sub><sup>2−</sup>, and Cd<sup>2+</sup> after 28 days of curing.</p>
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<p>Effects of Pb<sup>2+</sup>, CrO<sub>4</sub><sup>2−</sup>, Hg<sup>2+</sup>, and Cd<sup>2+</sup> content on the concentration in the TCLP extract, percentage of immobilization, and compressive strength of GP specimens after 28 days of curing: (<b>a</b>) Pb<sup>2+</sup>, (<b>b</b>) CrO<sub>4</sub><sup>2−</sup>, (<b>c</b>) Hg<sup>2+</sup>, and (<b>d</b>) Cd<sup>2+</sup>.</p>
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<p>Effects of Pb<sup>2+</sup>, CrO<sub>4</sub><sup>2−</sup>, Hg<sup>2+</sup>, and Cd<sup>2+</sup> content on the concentration in the TCLP extract, percentage of immobilization, and compressive strength of GP specimens after 28 days of curing: (<b>a</b>) Pb<sup>2+</sup>, (<b>b</b>) CrO<sub>4</sub><sup>2−</sup>, (<b>c</b>) Hg<sup>2+</sup>, and (<b>d</b>) Cd<sup>2+</sup>.</p>
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