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Materials Chemistry in Italy

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Materials Chemistry".

Deadline for manuscript submissions: closed (30 November 2022) | Viewed by 28118

Special Issue Editors

Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, CS, Italy
Interests: drug delivery systems; stimuli responsive polymers; functional polymers; carbon nanocomposites; polymer therapeutics
Special Issues, Collections and Topics in MDPI journals
Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy
Interests: design, synthesis and characterization of polymer nanoparticles and hydrogels; synthesis and characterization of stimuli-responsive micro- and nanoparticle systems for controlled drug release
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

This Special Issue aims to highlight academic research in Italy on Materials Chemistry Field, including all the aspects of either synthesis and characterization of new materials, or the evaluation of un-expected properties of known materials, as well as any aspect related to this topic. The Special Issue attempts to bring together representative examples of the research in progress in a multidisciplinary scenario, including chemistry physics, biomedicine, and engineering. In this context, Italian researchers have been investigating a wide variety of subjects and promoted innovative researches on different kinds of materials, including organic and inorganic materials, as well as biomaterials, composite and hybrid systems.

Papers within the scope of the issue are both research articles showing key researches or review papers overviewing the recent advances in the field with a critical evaluation of the strength and the weakness of the recent progress in the materials chemistry.

Prof. Dr. Francesca Iemma
Dr. Manuela Curcio
Dr. Alessia Irrera
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Molecules is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • materials chemistry
  • functional materials
  • composite materials
  • biomedical applications

Published Papers (15 papers)

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Research

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18 pages, 2560 KiB  
Article
Nanoparticle-Imprinted Silica Gel for the Size-Selective Capture of Silver Ultrafine Nanoparticles from Water
by Piersandro Pallavicini, Luca Preti, Maria L. Protopapa, Daniela Carbone, Laura Capodieci, Yuri A. Diaz Fernandez, Chiara Milanese, Angelo Taglietti and Lavinia Doveri
Molecules 2023, 28(10), 4026; https://doi.org/10.3390/molecules28104026 - 11 May 2023
Viewed by 1557
Abstract
A synthetic approach has been developed to prepare silica gel monoliths that embed well separated silver or gold spherical nanoparticles (NP), with diameters of 8, 18 and 115 nm. Fe3+, O2/cysteine and HNO3 were all successfully used to [...] Read more.
A synthetic approach has been developed to prepare silica gel monoliths that embed well separated silver or gold spherical nanoparticles (NP), with diameters of 8, 18 and 115 nm. Fe3+, O2/cysteine and HNO3 were all successfully used to oxidize and remove silver NP from silica, while aqua regia was necessary for gold NP. In all cases, NP-imprinted silica gel materials were obtained, with spherical voids of the same dimensions of the dissolved particles. By grinding the monoliths, we prepared NP-imprinted silica powders that were able to efficiently reuptake silver ultrafine NP (Ag-ufNP, d = 8 nm) from aqueous solutions. Moreover, the NP-imprinted silica powders showed a remarkable size selectivity, based on the best match between NP radius and the curvature radius of the cavities, driven by the optimization of attractive Van der Waals forces between SiO2 and NP. Ag-ufNP are increasingly used in products, goods, medical devices, disinfectants, and their consequent diffusion in the environment is of rising concern. Although limited here to a proof-of-concept level, the materials and methods described in this paper may be an efficient solution for capturing Ag-ufNP from environmental waters and to safely dispose them. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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11 pages, 3465 KiB  
Article
Self-Assembly and Electrical Conductivity of a New [1]benzothieno[3,2-b][1]-benzothiophene (BTBT)-Peptide Hydrogel
by Anna Fortunato, Rafael Cintra Hensel, Stefano Casalini and Miriam Mba
Molecules 2023, 28(7), 2917; https://doi.org/10.3390/molecules28072917 - 24 Mar 2023
Cited by 2 | Viewed by 1251
Abstract
The conjugation of small-molecule semiconductors with self-assembling peptides is a powerful tool for the fabrication of supramolecular soft materials for organic electronics and bioelectronics. Herein, we introduced the benchmark organic semiconductor [1]benzothieno[3,2-b][1]-benzothiophene (BTBT) within the structure of a self-assembling amphipathic peptide. The molecular [...] Read more.
The conjugation of small-molecule semiconductors with self-assembling peptides is a powerful tool for the fabrication of supramolecular soft materials for organic electronics and bioelectronics. Herein, we introduced the benchmark organic semiconductor [1]benzothieno[3,2-b][1]-benzothiophene (BTBT) within the structure of a self-assembling amphipathic peptide. The molecular structure of the conjugate was rationally designed to favour π-π stacking between BTBT cores and π-delocalization within the self-assembled architectures. Hydrogels with fibrillar structure were obtained upon self-assembly. Spectroscopic studies confirmed that both hydrogen bonding between peptide segments and π-π stacking between BTBT chromophores are responsible for the formation of the 3D fibrillar network observed by transmission electron microscopy. The hydrogel was successfully deposited on gold interdigitated electrodes and a conductivity up to 1.6 (±0.1) × 10−5 S cm−1 was measured. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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15 pages, 3867 KiB  
Article
Peculiar Properties of the La0.25Ba0.25Sr0.5Co0.8Fe0.2O3−δ Perovskite as Oxygen Reduction Electrocatalyst
by Chiara Aliotta, Maria Costa, Leonarda Francesca Liotta, Valeria La Parola, Giuliana Magnacca and Francesca Deganello
Molecules 2023, 28(4), 1621; https://doi.org/10.3390/molecules28041621 - 08 Feb 2023
Viewed by 1314
Abstract
The electrochemical reduction of molecular oxygen is a fundamental process in Solid Oxide Fuel Cells and requires high efficiency cathode materials. Two La0.25Ba0.25Sr0.5Co0.8Fe0.2O3−δ-based perovskite compounds were prepared by solution combustion synthesis, [...] Read more.
The electrochemical reduction of molecular oxygen is a fundamental process in Solid Oxide Fuel Cells and requires high efficiency cathode materials. Two La0.25Ba0.25Sr0.5Co0.8Fe0.2O3−δ-based perovskite compounds were prepared by solution combustion synthesis, and characterized for their structural, microstructural, surface, redox and electrochemical properties as potential cathodes in comparison with Ba0.5Sr0.5Co0.8Fe0.2O3−δ and La0.5Sr0.5Co0.8Fe0.2O3−δ perovskites. Results highlighted that calcination at 900 °C led to a “bi-perovskite heterostructure”, where two different perovskite structures coexist, whereas at higher calcination temperatures a single-phase perovskite was formed. The results showed the effectiveness of the preparation procedures in co-doping the A-site of perovskites with barium and lanthanum as a strategy to optimize the cathode’s properties. The formation of nanometric heterostructure co-doped in the A-site evidenced an improvement in oxygen vacancies’ availability and in the redox properties, which promoted both processes: oxygen adsorption and oxygen ions drift, through the cathode material, to the electrolyte. A reduction in the total resistance was observed in the case of heterostructured material. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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13 pages, 1966 KiB  
Article
The Quest for Green Solvents for the Sustainable Production of Nanosheets of Two-Dimensional (2D) Materials, a Key Issue in the Roadmap for the Ecology Transition in the Flatland
by Jessica Occhiuzzi, Grazia Giuseppina Politano, Gianluca D’Olimpio and Antonio Politano
Molecules 2023, 28(3), 1484; https://doi.org/10.3390/molecules28031484 - 03 Feb 2023
Cited by 7 | Viewed by 1752
Abstract
The recent advent of two-dimensional (2D) materials has had a ground-breaking impact on science and technology. To exploit in technology their unique thickness-dependent physicochemical properties, the large-scale production of 2D materials is mandatory, but it represents an open challenge still due to various [...] Read more.
The recent advent of two-dimensional (2D) materials has had a ground-breaking impact on science and technology. To exploit in technology their unique thickness-dependent physicochemical properties, the large-scale production of 2D materials is mandatory, but it represents an open challenge still due to various pitfalls and severe limitations including the toxicity of state-of-the-art solvents. Thus, liquid-phase exfoliation based on green and bioderived solvents represents an ideal methodology for massive production. This is particularly crucial for introducing 2D materials in technological applications such as the production of drinking water and agri-food industrial processes. Here, we assessed the production of 2D nanosheets (specifically, graphene, WS2, MoS2) with liquid-phase exfoliation assisted by eco-friendly solvents, with a comparative evaluation of green solvents in terms of the yield and, moreover, the aspect ratio, defectivity, and crystalline quality of the produced nanosheets. In particular, we focus on the most promising green solvents in terms of the yield and the crystalline quality of the produced nanosheets: Polarclean, Iris, and Cyrene, which were compared with acetone/water mixtures, isopropyl alcohol (IPA), triethanolamine (TEA), aqueous solutions of urea, and an ethanol/water mixture as well as two toxic solvents largely used for the production of 2D nanosheets: N-methyl-2-pyrrolidone (NMP) and N, N-dimethylformamide (DMF). Remarkably, the density of defects was particularly low in the liquid-phase exfoliation with Polarclean, as indicated by the Raman spectrum of graphene, with the I(D)/I(G) ratio below 0.1. Furthermore, Polarclean and Iris also enable ink-jet printing with functional inks of 2D materials based on green solvents due to their low dynamic viscosity at room temperature. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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10 pages, 9262 KiB  
Article
Carboxymethylcellulose-Based Hydrogel Obtained from Bacterial Cellulose
by Sanosh Kunjalukkal Padmanabhan, Leonardo Lamanna, Marco Friuli, Alessandro Sannino, Christian Demitri and Antonio Licciulli
Molecules 2023, 28(2), 829; https://doi.org/10.3390/molecules28020829 - 13 Jan 2023
Cited by 7 | Viewed by 1886
Abstract
In the present study, we have produced a sodium carboxymethylcellulose (CMC) hydrogel from a bacterial cellulose etherification reaction with chloroacetic acid in an alkaline medium. Bacterial cellulose (BC) was synthesized via economical and environmentally friendly methods using the Gluconacetobacter xylinus bacterium. After purification, [...] Read more.
In the present study, we have produced a sodium carboxymethylcellulose (CMC) hydrogel from a bacterial cellulose etherification reaction with chloroacetic acid in an alkaline medium. Bacterial cellulose (BC) was synthesized via economical and environmentally friendly methods using the Gluconacetobacter xylinus bacterium. After purification, freeze-drying, and milling, BC microparticles were dispersed in NaOH solution for different time periods before the etherification reaction. This has allowed the understanding of the alkalinization effect on BC modification. All synthesized CMC were soluble in water, and FTIR and XRD analyses confirmed the etherification reaction. The bath of BC in NaOH solution affects both molecular weight and degree of substitution. SEM analysis revealed the change of BC microstructure from fibrous-like to a smooth, uniform structure. The CMC-0 h allowed the production of crosslinked hydrogel after dehydrothermal treatment. Such hydrogel has been characterized rheologically and has shown a water absorption of 35 times its original weight. The optimization of the CMC produced from BC could pave the way for the production of ultrapure hydrogel to be applied in the healthcare and pharmaceutical industry. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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28 pages, 6030 KiB  
Article
Development of Tailored Graphene Nanoparticles: Preparation, Sorting and Structure Assessment by Complementary Techniques
by Kaiyue Hu, Luigi Brambilla, Patrizia Sartori, Claudia Moscheni, Cristiana Perrotta, Lucia Zema, Chiara Bertarelli and Chiara Castiglioni
Molecules 2023, 28(2), 565; https://doi.org/10.3390/molecules28020565 - 05 Jan 2023
Cited by 1 | Viewed by 1438
Abstract
We present a thorough structural characterization of Graphene Nano Particles (GNPs) prepared by means of physical procedures, i.e., ball milling and ultra-sonication of high-purity synthetic graphite. UV-vis absorption/extinction spectroscopy, Dynamic Light Scattering, Transmission Electron Microscopy, IR and Raman spectroscopies were performed. Particles with [...] Read more.
We present a thorough structural characterization of Graphene Nano Particles (GNPs) prepared by means of physical procedures, i.e., ball milling and ultra-sonication of high-purity synthetic graphite. UV-vis absorption/extinction spectroscopy, Dynamic Light Scattering, Transmission Electron Microscopy, IR and Raman spectroscopies were performed. Particles with small size were obtained, with an average lateral size <L> = 70–120 nm, formed by few <N> = 1–10 stacked layers, and with a small number of carboxylic groups on the edges. GNPs relatively more functionalized were separated by centrifugation, which formed stable water dispersions without the need for any surfactant. A critical reading and unified interpretation of a wide set of spectroscopic data was provided, which demonstrated the potential of Specular Reflectance Infrared Spectroscopy for the diagnosis and quantification of chemical functionalization of GNPs. Raman parameters commonly adopted for the characterization of graphitic materials do not always follow a monotonic trend, e.g., with the particle size and shape, thus unveiling some limitations of the available spectroscopic metrics. This issue was overcome thanks to a comparative spectra analysis, including spectra deconvolution by means of curve fitting procedures, experiments on reference materials and the exploitation of complementary characterization techniques. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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21 pages, 4792 KiB  
Article
Rosmarinic and Glycyrrhetinic Acid-Modified Layered Double Hydroxides as Functional Additives for Poly(Lactic Acid)/Poly(Butylene Succinate) Blends
by Francesca Cicogna, Elisa Passaglia, Matilde Benedettini, Werner Oberhauser, Randa Ishak, Francesca Signori and Serena Coiai
Molecules 2023, 28(1), 347; https://doi.org/10.3390/molecules28010347 - 01 Jan 2023
Cited by 8 | Viewed by 1790
Abstract
Immobilizing natural antioxidant and biologically active molecules in layered double hydroxides (LDHs) is an excellent method to retain and release these substances in a controlled manner, as well as protect them from thermal and photochemical degradation. Herein, we describe the preparation of host–guest [...] Read more.
Immobilizing natural antioxidant and biologically active molecules in layered double hydroxides (LDHs) is an excellent method to retain and release these substances in a controlled manner, as well as protect them from thermal and photochemical degradation. Herein, we describe the preparation of host–guest systems based on LDHs and rosmarinic and glycyrrhetinic acids, two molecules obtained from the extraction of herbs and licorice root, respectively, with antioxidant, antimicrobial, and anti-inflammatory properties. Intercalation between the lamellae of the mono-deprotonated anions of rosmarinic and glycyrrhetinic acid (RA and GA), alone or in the presence of an alkyl surfactant, allows for readily dispersible systems in biobased polymer matrices such as poly(lactic acid) (PLA), poly(butylene succinate) (PBS), and a 60/40 wt./wt. PLA/PBS blend. The composites based on the PLA/PBS blend showed better interphase compatibility than the neat blend, correlated with increased adhesion at the interface and a decreased dispersed phase size. In addition, we proved that the active species migrate slowly from thin films of the composite materials in a hydroalcoholic solvent, confirming the optimization of the release process. Finally, both host–guest systems and polymeric composites showed antioxidant capacity and, in the case of the PLA composite containing LDH-RA, excellent inhibitory capacity against E. coli and S. aureus. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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18 pages, 4632 KiB  
Article
Surface Functionalization of Face Masks with Cold Plasma and Its Effect in Anchoring Polyphenols Extracted from Agri-Food
by Francesca Cicogna, Emilia Bramanti, Beatrice Campanella, Stefano Caporali, Luca Panariello, Caterina Cristallini, Randa Ishak, Niccoletta Barbani, Elisa Passaglia and Serena Coiai
Molecules 2022, 27(23), 8632; https://doi.org/10.3390/molecules27238632 - 06 Dec 2022
Cited by 1 | Viewed by 1343
Abstract
To improve the capability of non-woven polypropylene-based fabric (NWF-PP) used for face mask production to retain active biomolecules such as polyphenols, the surface functionalization of NWF-PP–directly cut from face masks–was carried out by employing cold plasma with oxygen. The nature/structure of the functional [...] Read more.
To improve the capability of non-woven polypropylene-based fabric (NWF-PP) used for face mask production to retain active biomolecules such as polyphenols, the surface functionalization of NWF-PP–directly cut from face masks–was carried out by employing cold plasma with oxygen. The nature/structure of the functional groups, as well as the degree of functionalization, were evaluated by ATR-FTIR and XPS by varying the experimental conditions (generator power, treatment time, and oxygen flow). The effects of plasma activation on mechanical and morphological characteristics were evaluated by stress–strain measurements and SEM analysis. The ability of functionalized NWF-PP to firmly anchor polyphenols extracted from cloves was estimated by ATR-FTIR analysis, IR imaging, extractions in physiological solution, and OIT analysis (before and after extraction), as well as by SEM analysis. All the results obtained converge in showing that, although the plasma treatment causes changes–not only on the surface–with certain detriment to the mechanical performance of the NWF-PP, the incorporated functionalities are able to retain/anchor the active molecules extracted from the cloves, thus stabilizing the treated surfaces against thermo-oxidation even after prolonged extraction. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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14 pages, 440 KiB  
Article
The Kinetics of Sorption–Desorption Phenomena: Local and Non-Local Kinetic Equations
by Giovanni Barbero, Antonio M. Scarfone and Luiz R. Evangelista
Molecules 2022, 27(21), 7601; https://doi.org/10.3390/molecules27217601 - 05 Nov 2022
Cited by 2 | Viewed by 1191
Abstract
The kinetics of adsorption phenomena are investigated in terms of local and non-local kinetic equations of the Langmuir type. The sample is assumed in the shape of a slab, limited by two homogeneous planar-parallel surfaces, in such a manner that the problem can [...] Read more.
The kinetics of adsorption phenomena are investigated in terms of local and non-local kinetic equations of the Langmuir type. The sample is assumed in the shape of a slab, limited by two homogeneous planar-parallel surfaces, in such a manner that the problem can be considered one-dimensional. The local kinetic equations in time are analyzed when both saturation and non-saturation regimes are considered. These effects result from an extra dependence of the adsorption coefficient on the density of adsorbed particles, which implies the consideration of nonlinear balance equations. Non-local kinetic equations, arising from the existence of a time delay characterizing a type of reaction occurring between a bulk particle and the surface, are analyzed and show the existence of adsorption effects accompanied by temporal oscillations. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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10 pages, 1991 KiB  
Article
Effect of Formic Acid on the Outdiffusion of Ti Interstitials at TiO2 Surfaces: A DFT+U Investigation
by Daniel Forrer and Andrea Vittadini
Molecules 2022, 27(19), 6538; https://doi.org/10.3390/molecules27196538 - 03 Oct 2022
Cited by 2 | Viewed by 1039
Abstract
Ti interstitials play a key role in the surface chemistry of TiO2. However, because of their elusive behavior, proof of their participation in catalytic processes is difficult to obtain. Here, we used DFT+U calculations to investigate the interaction between formic acid [...] Read more.
Ti interstitials play a key role in the surface chemistry of TiO2. However, because of their elusive behavior, proof of their participation in catalytic processes is difficult to obtain. Here, we used DFT+U calculations to investigate the interaction between formic acid (FA) and excess Ti atoms on the rutile-TiO2(110) and anatase-TiO2(101) surfaces. The excess Ti atoms favor FA dissociation, while decreasing the relative stability of the bidentate bridging coordination over the monodentate one. FA species interact significantly with the Ti interstitials, favoring their outdiffusion. Eventually, Ti atoms can emerge at the surface forming chelate species, which are more stable than monodentate FA species in the case of rutile, and are even energetically favored in the case of anatase. The presence of Ti adatoms that can directly participate to surface processes should then be considered when formic acid and possibly carboxylate-bearing species are adsorbed onto TiO2 particles. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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15 pages, 4669 KiB  
Article
Barium Titanate Functionalization with Organosilanes: Effect on Particle Compatibility and Permittivity in Nanocomposites
by Nico Zamperlin, Andrea Bottacini, Emanuela Callone, Alessandro Pegoretti, Marco Fontana and Sandra Dirè
Molecules 2022, 27(19), 6499; https://doi.org/10.3390/molecules27196499 - 01 Oct 2022
Cited by 3 | Viewed by 1793
Abstract
Barium titanate (BT) recently gained new interest in the preparation of dielectric and piezoelectric lead-free materials for applications in sensors, electronics, energy harvesting and storage fields. Barium titanate nanocomposites can achieve attractive performance, provided that the compatibility between ceramic particles and polymeric matrices [...] Read more.
Barium titanate (BT) recently gained new interest in the preparation of dielectric and piezoelectric lead-free materials for applications in sensors, electronics, energy harvesting and storage fields. Barium titanate nanocomposites can achieve attractive performance, provided that the compatibility between ceramic particles and polymeric matrices is enhanced to the benefit of the physical properties of the final composite. Tuning the particle–matrix interface through particle functionalization represents a viable solution. In this work, surface functionalization of BT nanoparticles (NPs), obtained by hydrothermal synthesis, with 3-glycidyloxypropyltrimethoxysilane, 2-[(acetoxy(polyethyleneoxy)propyl]triethoxysilane and triethoxysilylpropoxy(polyethyleneoxy)dodecanoate, was performed after optimizing the hydroxylation process of the NPs to improve their surface reactivity and increase the yield of grafting. Solid-state nuclear magnetic resonance and thermogravimetric analysis were used to quantify the molecules grafted onto the ceramic nanoparticles. Both bare and functionalized particles were employed in the realization of epoxy- and polydimethylsiloxane (PDMS)-based nanocomposites. Functionalization was proven to be beneficial for particle dispersibility and effective for particle alignment in the PDMS matrix. Moreover, the dielectric constant measurements revealed the potential of PDMS-based nanocomposites for applications in the field of dielectric elastomers. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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19 pages, 6409 KiB  
Article
Manufacturing of Fluff Pulp Using Different Pulp Sources and Bentonite on an Industrial Scale for Absorbent Hygienic Products
by Saeed Ismaeilimoghadam, Mehdi Sheikh, Pouyan Taheri, Sadegh Maleki, Hossien Resalati, Mehdi Jonoobi, Bahareh Azimi and Serena Danti
Molecules 2022, 27(15), 5022; https://doi.org/10.3390/molecules27155022 - 07 Aug 2022
Cited by 4 | Viewed by 3580
Abstract
In this study, for the first time, a composite fluff pulp was produced based on the combination of softwood (i.e., long-length fiber), hardwood (i.e., short-length fiber), non-wooden pulps (i.e., bagasse) and bentonite, with specific amounts to be used in hygienic pads (e.g., baby [...] Read more.
In this study, for the first time, a composite fluff pulp was produced based on the combination of softwood (i.e., long-length fiber), hardwood (i.e., short-length fiber), non-wooden pulps (i.e., bagasse) and bentonite, with specific amounts to be used in hygienic pads (e.g., baby diapers and sanitary napkins). After the defibration process, the manufactured fluff pulp was placed as an absorbent mass in diapers and sanitary napkins. Therefore, tests related to the fluff pulp, such as grammage, thickness, density, ash content, humidity percentage, pH and brightness, tests related to the manufactured baby diapers, such as absorption capacity, retention rate, retention capacity, absorption time and rewet, and tests related to the sanitary napkin, such as absorption capacity and rewet, were performed according to the related standards. The results demonstrated that increasing the amount of bagasse pulp led to increasing the ash content, pH and density of fluff pulp and decreasing the brightness. The addition of bentonite as a filler also increased ash content and pH of fluff pulp. The results also demonstrated that increasing of bagasse pulp up to 30% in combination with softwood pulp led to increasing absorption capacity, retention rate, retention capacity, absorption time and rewet of baby diapers and of sanitary napkins. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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15 pages, 2584 KiB  
Communication
Alginate Self-Crosslinking Ink for 3D Extrusion-Based Cryoprinting and Application for Epirubicin-HCl Delivery on MCF-7 Cells
by Giulia Remaggi, Ovidio Catanzano, Fabiana Quaglia and Lisa Elviri
Molecules 2022, 27(3), 882; https://doi.org/10.3390/molecules27030882 - 27 Jan 2022
Cited by 5 | Viewed by 3006
Abstract
3D-printed hydrogels are particularly advantageous as drug-delivery platforms but their loading with water-soluble active compounds remains a challenge requiring the development of innovative inks. Here, we propose a new 3D extrusion-based approach that, by exploiting the internal gelation of the alginate, avoids the [...] Read more.
3D-printed hydrogels are particularly advantageous as drug-delivery platforms but their loading with water-soluble active compounds remains a challenge requiring the development of innovative inks. Here, we propose a new 3D extrusion-based approach that, by exploiting the internal gelation of the alginate, avoids the post-printing crosslinking process and allows the loading of epirubicin-HCl (EPI). The critical combinations of alginate, calcium carbonate and d-glucono-δ-lactone (GDL) combined with the scaffold production parameters (extrusion time, temperature, and curing time) were evaluated and discussed. The internal gelation in tandem with 3D extrusion allowed the preparation of alginate hydrogels with a complex shape and good handling properties. The dispersion of epirubicin-HCl in the hydrogel matrix confirmed the potential of this self-crosslinking alginate-based ink for the preparation of 3D-printed drug-delivery platforms. Drug release from 3D-printed hydrogels was monitored, and the cytotoxic activity was tested against MCF-7 cells. Finally, the change in the expression pattern of anti-apoptotic, pro-apoptotic, and autophagy protein markers was monitored by liquid-chromatography tandem-mass-spectrometry after exposure of MCF-7 to the EPI-loaded hydrogels. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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Review

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19 pages, 3756 KiB  
Review
Bismuth-Based Halide Perovskites for Photocatalytic H2 Evolution Application
by Costanza Tedesco and Lorenzo Malavasi
Molecules 2023, 28(1), 339; https://doi.org/10.3390/molecules28010339 - 01 Jan 2023
Cited by 5 | Viewed by 2416
Abstract
Metal halide perovskites (MHPs), in particular lead-based perovskites, have earned recognized fame in several fields for their outstanding optoelectronic properties, including direct generation of free charge carriers, optimal ambipolar charge carrier transport properties, high absorption coefficient, point-defect tolerance, and compositional versatility. Nowadays, this [...] Read more.
Metal halide perovskites (MHPs), in particular lead-based perovskites, have earned recognized fame in several fields for their outstanding optoelectronic properties, including direct generation of free charge carriers, optimal ambipolar charge carrier transport properties, high absorption coefficient, point-defect tolerance, and compositional versatility. Nowadays, this class of materials represents a real and promising alternative to silicon for photovoltaic technologies. This worthy success led to a growing interest in the exploration of MHPs in other hot research fields, such as solar-driven photocatalytic water splitting towards hydrogen production. Nevertheless, many of these perovskites show air and moisture instability problems that considerably hinder their practical application for photocatalytic water splitting. Moreover, if chemical instability is a problem that can be in part mitigated by the optimization of the chemical composition and crystal structure, the presence of lead represents a real problem for the practical application of MHPs in commercial devices due to environmental and healthcare issues. To successfully overcome these problems, lead-free metal halide perovskites (LFMHPs) have gained increasing interest thanks to their optoelectronic properties, comparable to lead-based materials, and their more eco-friendly nature. Among all the lead-free perovskite alternatives, this mini-review considers bismuth-based perovskites and perovskite derivatives with a specific focus on solar-driven photocatalysis application for H2 evolution. Special attention is dedicated to the structure and composition of the different materials and to the advantage of heterojunction engineering and the relative impact on the photocatalytic process. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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18 pages, 4952 KiB  
Review
The Renewed Interest on Brunogeierite, GeFe2O4, a Rare Mineral of Germanium: A Review
by Marco Ambrosetti and Marcella Bini
Molecules 2022, 27(23), 8484; https://doi.org/10.3390/molecules27238484 - 02 Dec 2022
Cited by 2 | Viewed by 1312
Abstract
GeFe2O4, also known as brunogeierite, is a rare mineral of germanium. It has a normal spinel structure and, as with many other spinels, amazing functional properties thanks to its peculiar structural features. In the past, its spectroscopic, optical, magnetic [...] Read more.
GeFe2O4, also known as brunogeierite, is a rare mineral of germanium. It has a normal spinel structure and, as with many other spinels, amazing functional properties thanks to its peculiar structural features. In the past, its spectroscopic, optical, magnetic and electronic properties were determined; then, for many years, this compound was left behind. Only recently, a renewed interest in this oxide has arisen, particularly for its application in the electrochemical field. In this review paper, the crystal structure of GeFe2O4 will be described, as well as the synthesis methods required to obtain single crystals or polycrystalline powders. Its spectroscopic, magnetic, optical and electrical properties will be reported in detail. Then, successful applications known so far will be described: its use as anode in Lithium Ion and Sodium Ion Batteries and as electrocatalyst for urea oxidation reaction. Full article
(This article belongs to the Special Issue Materials Chemistry in Italy)
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