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Keywords = bio-solvents

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23 pages, 6941 KiB  
Article
Isolation and Characterization of Lignin from Sapele (Entandrophragma cylindricum): Application in Flexible Polyurethane Foam Production
by Hubert Justin Nnanga Guissele, Arnaud Maxime Cheumani Yona, Armel Edwige Mewoli, Désiré Chimeni-Yomeni, Lucioni Fabien Tsague, Tatiane Marina Abo, Jean-Bosco Saha-Tchinda, Maurice Kor Ndikontar and Antonio Pizzi
Polymers 2025, 17(15), 2156; https://doi.org/10.3390/polym17152156 - 6 Aug 2025
Abstract
Lignin used in this work was isolated from sapele (Entandrophragma cylindricum) wood through a hybrid pulping process using soda/ethanol as pulping liquor and denoted soda-oxyethylated lignin (SOL). SOL was mixed with a polyethylene glycol (PEG)–glycerol mixture (80/20 v/v) [...] Read more.
Lignin used in this work was isolated from sapele (Entandrophragma cylindricum) wood through a hybrid pulping process using soda/ethanol as pulping liquor and denoted soda-oxyethylated lignin (SOL). SOL was mixed with a polyethylene glycol (PEG)–glycerol mixture (80/20 v/v) as liquefying solvent with 98% wt. sulfur acid as catalyst, and the mixture was taken to boil at 140 °C for 2, 2.5, and 3 h. Three bio-polyols LBP1, LBP2, and LBP3 were obtained, and each of them exhibited a high proportion of -OH groups. Lignin-based polyurethane foams (LBPUFs) were prepared using the bio-polyols obtained with a toluene diisocyanate (TDI) prepolymer by the one-shot method. Gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FTIR), and carbon-13 nuclear magnetic resonance spectroscopy (13C NMR) were used characterize lignin in order to determine viscosity, yield, and composition and to characterize their structure. The PEG-400–glycerol mixture was found to react with the lignin bio-polyols’ phenolic -OHs. The bio-polyols’ viscosity was found to increase as the liquefaction temperature increased, while simultaneously their molecular weights decreased. All the NCO groups were eliminated from the samples, which had high thermal stability as the liquefaction temperature increased, leading to a decrease in cell size, density, and crystallinity and an improvement in mechanical performance. Based on these properties, especially the presence of some aromatic rings in the bio-polyols, the foams produced can be useful in automotive applications and for floor carpets. Full article
(This article belongs to the Section Circular and Green Sustainable Polymer Science)
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21 pages, 4264 KiB  
Article
Study on the Performance Restoration of Aged Asphalt Binder with Vegetable Oil Rejuvenators: Colloidal Stability, Rheological Properties, and Solubility Parameter Analysis
by Heng Yan, Xinxin Cao, Wei Wei, Yongjie Ding and Jukun Guo
Coatings 2025, 15(8), 917; https://doi.org/10.3390/coatings15080917 (registering DOI) - 6 Aug 2025
Abstract
This study evaluates the effectiveness of various rejuvenating oils, including soybean oil (N-oil), waste frying oil (F-oil), byproduct oil (W-oil), and aromatic hydrocarbon oil (A-oil), in restoring aged asphalt coatings by reducing asphaltene flocculation and improving colloidal stability. The rejuvenators were incorporated into [...] Read more.
This study evaluates the effectiveness of various rejuvenating oils, including soybean oil (N-oil), waste frying oil (F-oil), byproduct oil (W-oil), and aromatic hydrocarbon oil (A-oil), in restoring aged asphalt coatings by reducing asphaltene flocculation and improving colloidal stability. The rejuvenators were incorporated into aged asphalt binder via direct mixing at controlled dosages. Their effects were assessed using microscopy, droplet diffusion analysis, rheological testing (DSR and BBR), and molecular dynamics simulations. The aim is to compare the compatibility, solubility behavior, and rejuvenation potential of plant-based and mineral-based oils. The results indicate that N-oil and F-oil promote asphaltene aggregation, which supports structural rebuilding. In contrast, A-oil and W-oil act as solvents that disperse asphaltenes. Among the tested oils, N-oil exhibited the best overall performance in enhancing flowability, low-temperature flexibility, and chemical compatibility. This study presents a novel method to evaluate rejuvenator effectiveness by quantifying colloidal stability through grayscale analysis of droplet diffusion patterns. This integrated approach offers both mechanistic insights and practical guidance for selecting bio-based rejuvenators in asphalt recycling. Full article
(This article belongs to the Section Environmental Aspects in Colloid and Interface Science)
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16 pages, 1504 KiB  
Article
Tuning the Activity of NbOPO4 with NiO for the Selective Conversion of Cyclohexanone as a Model Intermediate of Lignin Pyrolysis Bio-Oils
by Abarasi Hart and Jude A. Onwudili
Energies 2025, 18(15), 4106; https://doi.org/10.3390/en18154106 - 2 Aug 2025
Viewed by 172
Abstract
Catalytic upgrading of pyrolysis oils is an important step for producing replacement hydrocarbon-rich liquid biofuels from biomass and can help to advance pyrolysis technology. Catalysts play a pivotal role in influencing the selectivity of chemical reactions leading to the formation of main compounds [...] Read more.
Catalytic upgrading of pyrolysis oils is an important step for producing replacement hydrocarbon-rich liquid biofuels from biomass and can help to advance pyrolysis technology. Catalysts play a pivotal role in influencing the selectivity of chemical reactions leading to the formation of main compounds in the final upgraded liquid products. The present work involved a systematic study of solvent-free catalytic reactions of cyclohexanone in the presence of hydrogen gas at 160 °C for 3 h in a batch reactor. Cyclohexanone can be produced from biomass through the selective hydrogenation of lignin-derived phenolics. Three types of catalysts comprising undoped NbOPO4, 10 wt% NiO/NbOPO4, and 30 wt% NiO/NbOPO4 were studied. Undoped NbOPO4 promoted both aldol condensation and the dehydration of cyclohexanol, producing fused ring aromatic hydrocarbons and hard char. With 30 wt% NiO/NbOPO4, extensive competitive hydrogenation of cyclohexanone to cyclohexanol was observed, along with the formation of C6 cyclic hydrocarbons. When compared to NbOPO4 and 30 wt% NiO/NbOPO4, the use of 10 wt% NiO/NbOPO4 produced superior selectivity towards bi-cycloalkanones (i.e., C12) at cyclohexanone conversion of 66.8 ± 1.82%. Overall, the 10 wt% NiO/NbOPO4 catalyst exhibited the best performance towards the production of precursor compounds that can be further hydrodeoxygenated into energy-dense aviation fuel hydrocarbons. Hence, the presence and loading of NiO was able to tune the activity and selectivity of NbOPO4, thereby influencing the final products obtained from the same cyclohexanone feedstock. This study underscores the potential of lignin-derived pyrolysis oils as important renewable feedstocks for producing replacement hydrocarbon solvents or feedstocks and high-density sustainable liquid hydrocarbon fuels via sequential and selective catalytic upgrading. Full article
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46 pages, 4006 KiB  
Review
Solvent-Driven Electroless Nickel Coatings on Polymers: Interface Engineering, Microstructure, and Applications
by Chenyao Wang, Heng Zhai, David Lewis, Hugh Gong, Xuqing Liu and Anura Fernando
Coatings 2025, 15(8), 898; https://doi.org/10.3390/coatings15080898 (registering DOI) - 1 Aug 2025
Viewed by 339
Abstract
Electroless nickel deposition (ELD) is an autocatalytic technique extensively used to impart conductive, protective, and mechanical functionalities to inherently non-conductive synthetic substrates. This review systematically explores the fundamental mechanisms of electroless nickel deposition, emphasising recent advancements in surface activation methods, solvent systems, and [...] Read more.
Electroless nickel deposition (ELD) is an autocatalytic technique extensively used to impart conductive, protective, and mechanical functionalities to inherently non-conductive synthetic substrates. This review systematically explores the fundamental mechanisms of electroless nickel deposition, emphasising recent advancements in surface activation methods, solvent systems, and microstructural control. Critical analysis reveals that bio-inspired activation methods, such as polydopamine (PDA) and tannic acid (TA), significantly enhance coating adhesion and durability compared to traditional chemical etching and plasma treatments. Additionally, solvent engineering, particularly using polar aprotic solvents like dimethyl sulfoxide (DMSO) and ethanol-based systems, emerges as a key strategy for achieving uniform, dense, and flexible coatings, overcoming limitations associated with traditional aqueous baths. The review also highlights that microstructural tailoring, specifically the development of amorphous-nanocrystalline hybrid nickel coatings, effectively balances mechanical robustness (hardness exceeding 800 HV), flexibility, and corrosion resistance, making these coatings particularly suitable for wearable electronic textiles and smart materials. Furthermore, commercial examples demonstrate the real-world applicability and market readiness of nickel-coated synthetic fibres. Despite significant progress, persistent challenges remain, including reliable long-term adhesion, internal stress management, and environmental sustainability. Future research should prioritise environmentally benign plating baths, standardised surface activation protocols, and scalable deposition processes to fully realise the industrial potential of electroless nickel coatings. Full article
(This article belongs to the Section Surface Characterization, Deposition and Modification)
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10 pages, 1225 KiB  
Article
Development of an LC-MS Method for the Analysis of Birch (Betula sp.) Bark Bioactives Extracted with Biosolvents
by Inmaculada Luque-Jurado, Jesús E. Quintanilla-López, Rosa Lebrón-Aguilar, Ana Cristina Soria and María Luz Sanz
Molecules 2025, 30(15), 3181; https://doi.org/10.3390/molecules30153181 - 29 Jul 2025
Viewed by 183
Abstract
Birch (Betula sp.) bark is a well-known natural source of betulin (Bet) and betulinic acid (BAc), both of which have several bioactive properties. The evaluation of the extraction performance, relative to these lupane-type triterpenoids, provided by different biosolvents requires the development of [...] Read more.
Birch (Betula sp.) bark is a well-known natural source of betulin (Bet) and betulinic acid (BAc), both of which have several bioactive properties. The evaluation of the extraction performance, relative to these lupane-type triterpenoids, provided by different biosolvents requires the development of a high-resolution and high-sensitivity liquid chromatography-mass spectrometry (LC-MS) approach that is also compatible with challenging extractants such as natural deep eutectic solvents (NADESs). In this work, an LC-MS method was developed and analytically characterized prior to its application for the quantitation of Bet and BAc in birch bark extracts obtained using conventional solvents (methanol and acetone) and biosolvents (limonene and NADESs). High precision (RSD < 3.3%), sensitivity (LOD: 23 ng mL−1 and 29 ng mL−1 for Bet and BAc, respectively), and accuracy (95–102% recovery) were found for this optimized method, using an acidulated water–methanol mixture as the mobile phase and sodium acetate as an additive. Extraction experiments conducted at 55 °C revealed that the NADESs, particularly thymol:1-octanol (1:1 molar ratio), outperformed the other solvents and were highly effective for the recovery of both triterpenoids (17.50 mg g−1 and 0.92 mg g−1 of Bet and BAc, respectively). This method can also be applied to similar extracts obtained from other biomasses. Full article
(This article belongs to the Special Issue New Advances in Deep Eutectic Solvents, 2nd Edition)
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29 pages, 3084 KiB  
Article
The Cascade Transformation of Furfural to Cyclopentanone: A Critical Evaluation Concerning Feasible Process Development
by Christian A. M. R. van Slagmaat
ChemEngineering 2025, 9(4), 74; https://doi.org/10.3390/chemengineering9040074 - 19 Jul 2025
Viewed by 279
Abstract
Furfural is a fascinating bio-based platform molecule that can be converted into useful cyclic compounds, among others. In this work, the hydrogenative rearrangement-dehydration of furfural towards cyclopentanone using a commercially available Pt/C catalyst was investigated in terms of its reaction performance to assess [...] Read more.
Furfural is a fascinating bio-based platform molecule that can be converted into useful cyclic compounds, among others. In this work, the hydrogenative rearrangement-dehydration of furfural towards cyclopentanone using a commercially available Pt/C catalyst was investigated in terms of its reaction performance to assess its feasibility as an industrial process. However, acquiring an acceptable cyclopentanone yield proved very difficult, and the reaction was constrained by unforeseen parameters, such as the relative liquid volume in the reactor and the substrate concentration. Most strikingly, the sacrificial formation of furanoic oligomers that precipitated onto the catalyst’s surface was a troublesome key factor that mediated the product’s selectivity versus the carbon mass balance. By applying a biphasic water–toluene solvent system, the yield of cyclopentanone was somewhat improved to a middling 59%, while tentatively positive distributions of reaction components over these solvent phases were observed, which could be advantageous for anticipated down-stream processing. Overall, the sheer difficulty of controlling this one-pot cascade transformation towards a satisfactory product output under rather unfavorable reaction parameters renders it unsuitable for industrial process development, and a multi-step procedure for this chemical transformation might be considered instead. Full article
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13 pages, 2599 KiB  
Article
Enhancement of Dimensional Stability, Hydrophobicity, and Mechanical Strength of North American Red Alder Wood Through Silane Impregnation Combined with DES Pretreatment
by Yang Zheng, Ting Zhou, Chenyang Cai and Honghai Liu
Forests 2025, 16(7), 1152; https://doi.org/10.3390/f16071152 - 12 Jul 2025
Viewed by 240
Abstract
Wood is a green and renewable bio-based building material, but its hygroscopicity affects its dimensional stability, limiting its use in construction. Chemical modification can improve its properties, yet its effectiveness depends on wood permeability and traditional modifiers. This study first used a deep [...] Read more.
Wood is a green and renewable bio-based building material, but its hygroscopicity affects its dimensional stability, limiting its use in construction. Chemical modification can improve its properties, yet its effectiveness depends on wood permeability and traditional modifiers. This study first used a deep eutectic solvent (DES) to boost the permeability of North American alder wood. Then, methyl trimethoxysilane was impregnated under supercritical carbon dioxide (SCI), pressure (PI), vacuum (VI), and atmospheric pressure (AI) conditions. DES treatment damaged the cell structure, increasing wood permeability. Silane was deposited and polymerized in the cell lumen, chemically bonding with cell-wall components, filling walls and pits, and thickening walls. The VI group had the highest absolute density (0.59 g/cm3, +36.6%) and the lowest moisture absorption (4.4%, −33.3%). The AI group had the highest ASE (25%). The PI group showed the highest surface hardness (RL, 2592 N) and a water contact angle of 131.9°, much higher than natural wood. Overall, the VI group had the best performance. Silane reacts with cellulose, hemicellulose, and lignin in wood via hydrolysis and hydroxyl bonding, forming stable bonds that enhance the treated wood’s hydrophobicity, dimensional stability, and surface hardness. Full article
(This article belongs to the Section Wood Science and Forest Products)
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18 pages, 1085 KiB  
Article
Overcoming the Reversibility in the Diels–Alder Reaction of Bio-Based Electron-Poor Furans with Maleimides Through Liquid-to-Solid Phase Transition
by Konstantin I. Galkin, Daria V. Zakharova, Rinat R. Aysin, Anastasia A. Danshina, Alexandra M. Pak, Irina V. Sandulenko, Roman A. Novikov and Ksenia S. Egorova
Int. J. Mol. Sci. 2025, 26(14), 6550; https://doi.org/10.3390/ijms26146550 - 8 Jul 2025
Viewed by 424
Abstract
In the chemistry of bio-based furans, the Diels–Alder reaction plays an important role as a renewable route for the synthesis of fuels, fine chemicals, and monomers. Nonetheless, the unfavorable kinetic and thermodynamic parameters inherent to the Diels–Alder reaction involving furans as dienes often [...] Read more.
In the chemistry of bio-based furans, the Diels–Alder reaction plays an important role as a renewable route for the synthesis of fuels, fine chemicals, and monomers. Nonetheless, the unfavorable kinetic and thermodynamic parameters inherent to the Diels–Alder reaction involving furans as dienes often lead to the reversibility of cycloaddition, resulting in decreased equilibrium conversion and diastereoselectivity. In this study, we present a new strategy for overcoming the problem of reversibility in chemical reactions. We demonstrate that conducting the reaction under solvent-free conditions can facilitate the transition from a molten state formed by the initial reactants to a solid phase containing the reaction product along with an excess of the initial substrate. According to our results, such a liquid-to-solid transition of the reaction mixture can lead to exceptionally high conversion and diastereoselectivity in the furan–maleimide Diels–Alder reaction, particularly for challenging electron-poor furanic substrates. Our approach enables the reversible furan–maleimide Diels–Alder reaction to be performed in a cleaner and more environmentally friendly manner, free from the complexities associated with the use of solvents and the need for purification from side products. Full article
(This article belongs to the Section Physical Chemistry and Chemical Physics)
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42 pages, 1721 KiB  
Review
Electrospinning Enables Opportunity for Green and Effective Antibacterial Coatings of Medical Devices
by Saverio Caporalini, Bahareh Azimi, Samir Zergat, Mahdi Ansari Chaharsoughi, Homa Maleki, Giovanna Batoni and Serena Danti
J. Funct. Biomater. 2025, 16(7), 249; https://doi.org/10.3390/jfb16070249 - 6 Jul 2025
Cited by 1 | Viewed by 1018
Abstract
The growing antimicrobial resistance and the increasing environmental concerns associated with conventional antibacterial agents have prompted a search for more effective and sustainable alternatives. Biopolymer-based nanofibers are promising candidates to produce environment-friendly antibacterial coatings, owing to their high surface-to-volume ratio, structural adaptability, and [...] Read more.
The growing antimicrobial resistance and the increasing environmental concerns associated with conventional antibacterial agents have prompted a search for more effective and sustainable alternatives. Biopolymer-based nanofibers are promising candidates to produce environment-friendly antibacterial coatings, owing to their high surface-to-volume ratio, structural adaptability, and tunable porosity. These features make them particularly well-suited for delivering antimicrobial agents in a controlled manner and for physically modifying the surface of medical devices. This review critically explores recent advances in the use of electrospun fibers enhanced with natural antimicrobial agents as eco-friendly surface coatings. The mechanisms of antibacterial action, key factors affecting their efficacy, and comparisons with conventional antibacterial agents are discussed herein. Emphasis is placed on the role of a “green electrospinning” process, which utilizes bio-based materials and nontoxic solvents, to enable coatings able to better combat antibiotic-resistant pathogens. Applications in various clinical settings, including implants, wound dressings, surgical textiles, and urinary devices, are explored. Finally, the environmental benefits and prospects for the scalability and sustainability of green coatings are discussed to underscore their relevance to next-generation, sustainable solutions in healthcare. Full article
(This article belongs to the Special Issue Advanced Technologies for Processing Functional Biomaterials)
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22 pages, 3243 KiB  
Article
Development of a Continuous Extrusion Process for Alginate Biopolymer Films for Sustainable Applications
by Zahra Eslami, Saïd Elkoun, Miraidin Mirzapour and Mathieu Robert
Polymers 2025, 17(13), 1818; https://doi.org/10.3390/polym17131818 - 29 Jun 2025
Viewed by 714
Abstract
This study presents a novel method for producing extrudable alginate-based films using continuous thermo-mechanical mixing, providing a scalable alternative to conventional solvent-casting techniques. The effects of glycerol concentration (30–50 wt%) and processing temperature (110–120 °C) on the films’ thermal, mechanical, and structural properties [...] Read more.
This study presents a novel method for producing extrudable alginate-based films using continuous thermo-mechanical mixing, providing a scalable alternative to conventional solvent-casting techniques. The effects of glycerol concentration (30–50 wt%) and processing temperature (110–120 °C) on the films’ thermal, mechanical, and structural properties were systematically investigated. Structural characterization was performed using 1H NMR and FT-IR, and thermal transitions were analyzed via DSC (Differential Scanning Calorimetry) and DMA (Dynamic Mechanical Analysis). The glass transition temperature (Tg) of the alginate/glycerol/water system was modeled using the Gordon–Taylor equation. Glycerol incorporation significantly reduced Tg—by up to 76 °C with 40 wt% glycerol—and enhanced ductility and toughness, reaching 3.26 MJ/m3 at the optimal level. The influence of processing temperature was found to depend on plasticizer content: at lower glycerol levels, elevated temperatures decreased Tg and elongation at break, likely due to thermal degradation. However, films with higher glycerol content retained stable mechanical and thermal behavior across both temperature profiles. This work is among the first to explore how processing temperature affects extruded, plasticized pure alginate films. The findings provide key insights into the formulation and scalable production of bio-based packaging materials, highlighting the importance of optimizing both plasticizer concentration and processing parameters. Full article
(This article belongs to the Special Issue Recent Advances and Applications of Polymer Nanocomposites)
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50 pages, 8944 KiB  
Review
Fire-Resistant Coatings: Advances in Flame-Retardant Technologies, Sustainable Approaches, and Industrial Implementation
by Rutu Patel, Mayankkumar L. Chaudhary, Yashkumar N. Patel, Kinal Chaudhari and Ram K. Gupta
Polymers 2025, 17(13), 1814; https://doi.org/10.3390/polym17131814 - 29 Jun 2025
Viewed by 1534
Abstract
Fire-resistant coatings have emerged as crucial materials for reducing fire hazards in various industries, including construction, textiles, electronics, and aerospace. This review provides a comprehensive account of recent advances in fire-resistant coatings, emphasizing environmentally friendly and high-performance systems. Beginning with a classification of [...] Read more.
Fire-resistant coatings have emerged as crucial materials for reducing fire hazards in various industries, including construction, textiles, electronics, and aerospace. This review provides a comprehensive account of recent advances in fire-resistant coatings, emphasizing environmentally friendly and high-performance systems. Beginning with a classification of traditional halogenated and non-halogenated flame retardants (FRs), this article progresses to cover nitrogen-, phosphorus-, and hybrid-based systems. The synthesis methods, structure–property relationships, and fire suppression mechanisms are critically discussed. A particular focus is placed on bio-based and waterborne formulations that align with green chemistry principles, such as tannic acid (TA), phytic acid (PA), lignin, and deep eutectic solvents (DESs). Furthermore, the integration of nanomaterials and smart functionalities into fire-resistant coatings has demonstrated promising improvements in thermal stability, char formation, and smoke suppression. Applications in real-world contexts, ranging from wood and textiles to electronics and automotive interiors, highlight the commercial relevance of these developments. This review also addresses current challenges such as long-term durability, environmental impacts, and the standardization of performance testing. Ultimately, this article offers a roadmap for developing safer, sustainable, and multifunctional fire-resistant coatings for future materials engineering. Full article
(This article belongs to the Special Issue Flame-Retardant Polymer Composites II)
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22 pages, 1280 KiB  
Article
Dimethyl Isosorbide: An Innovative Bio-Renewable Solvent for Sustainable Chromatographic Applications
by Aleksandra Damjanoska, Kristina Mitreska, Matilda Petrova, Jelena Acevska, Katerina Brezovska and Natalija Nakov
Molecules 2025, 30(13), 2713; https://doi.org/10.3390/molecules30132713 - 24 Jun 2025
Viewed by 1113
Abstract
The increasing environmental concerns and regulatory restrictions on toxic conventional solvents have driven the search for sustainable alternatives. Dimethyl isosorbide (DMI), a bio-renewable solvent, has shown potential as a replacement for short-chain glycol ethers, although its use as solvent in liquid chromatography (LC) [...] Read more.
The increasing environmental concerns and regulatory restrictions on toxic conventional solvents have driven the search for sustainable alternatives. Dimethyl isosorbide (DMI), a bio-renewable solvent, has shown potential as a replacement for short-chain glycol ethers, although its use as solvent in liquid chromatography (LC) is underexplored. This study presents a physicochemical characterization of DMI with a particular focus on its application as an innovative solvent in LC analyses. The partition coefficient (log P = −0.44) was determined using the OECD 107 method, and viscosity measurements for DMI and its mixtures with water and ethanol were conducted at 25 °C, 40 °C, and 60 °C. Viscosity ranged from 1.28 mPa·s at 60 °C to 2.62 mPa·s at 40 °C. The Central Composite Face 23 experimental design for studying the chromatographic behavior of DMI confirmed that 50% (v/v) DMI can be effectively utilized in the mobile phases, at a column temperature of 40 °C, with backpressures ranging from 160 to 300 bar and a UV cut-off at 240 nm. Its effectiveness as an eluent in LC was demonstrated for the quantification of methylparaben and propylparaben in pharmaceutical formulations. This study highlights DMI’s promise as a sustainable bio-renewable alternative to conventional organic solvents used as eluents in LC, supporting eco-friendly practices in pharmaceutical analysis. Full article
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16 pages, 3109 KiB  
Article
Mitigating Shrinkage and Enhancing the Structure of Thermally Insulating Starch Aerogel via Solvent Exchange and Chitin Addition
by Jacob Staker, Gracie M. White, Sevinch Pasilova, Daniel A. Scheiman, Haiquan Guo, Andres Tovar and Amanda P. Siegel
Macromol 2025, 5(2), 28; https://doi.org/10.3390/macromol5020028 - 18 Jun 2025
Cited by 1 | Viewed by 419
Abstract
Bio-based compostable starch aerogels have significant potential as a sustainable alternative to traditional polymer aerogels across various applications. However, they suffer from very significant shrinkage, shown in published work as 40–50% using existing processes. We hypothesized that the shrinkage is largely caused by [...] Read more.
Bio-based compostable starch aerogels have significant potential as a sustainable alternative to traditional polymer aerogels across various applications. However, they suffer from very significant shrinkage, shown in published work as 40–50% using existing processes. We hypothesized that the shrinkage is largely caused by pore collapse through the solvent exchange process, during which the water used to fabricate the starch matrix is replaced with ethanol. To mitigate this issue, this work introduces two strategies: (1) implementing a deep-freezing protocol (DFP) prior to the solvent exchange, followed by pure ethanol solvent exchanges instead of water/ethanol mixtures, and (2) incorporating chitin as a structural additive. As a baseline, we fabricated potato starch aerogels (PSAs) using conventional processes of mixing, heating, and retrogradation. By applying a DFP before pure ethanol exchanges, shrinkage was reduced from 44% to 10% in pure PSA samples. Furthermore, the addition of chitin reduced shrinkage to 8% in potato starch-chitin aerogels. Porosity, density, surface area, pore size distribution, thermal decomposition temperature, thermal conductivities, and scanning electron microscopy images demonstrate a correlation between reduced shrinkage and desired thermal material properties. Full article
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23 pages, 4150 KiB  
Article
Optimized Coagulation Flocculation of Drinking Water Using Pine cone-Based Bio-Coagulants: A Comparative Study of Different Extracts
by Ouiem Baatache, Abderrezzaq Benalia, Kerroum Derbal, Amel Khalfaoui and Antonio Pizzi
Water 2025, 17(12), 1793; https://doi.org/10.3390/w17121793 - 15 Jun 2025
Viewed by 558
Abstract
High turbidity in raw water poses a major challenge to drinking water quality and requires effective, sustainable treatment solutions. This work investigates the reduction in turbidity in raw water and the enhancement of overall drinking water quality through the coagulation–flocculation process. The performance [...] Read more.
High turbidity in raw water poses a major challenge to drinking water quality and requires effective, sustainable treatment solutions. This work investigates the reduction in turbidity in raw water and the enhancement of overall drinking water quality through the coagulation–flocculation process. The performance of Pine cone extract as a bio-coagulant was evaluated using four different solvent-based extractions (PC-H2O, PC-HCl, PC-NaCl, and PC-NaOH). The effects of key operational parameters were analyzed, and jar tests were carried out to enhance the coagulation–flocculation process by identifying the optimal conditions. Experimental design was further refined using RSM based on a BBD, incorporating three factors: initial pH, coagulant dosage, and settling time, with turbidity removal efficiency as the response variable. Statistical analysis confirmed that initial pH, coagulant dosage, and settling time significantly influenced turbidity reduction at a confidence level of p-value < 0.05 for all four solvents. Among the extracts tested, PC-HCl demonstrated the highest turbidity removal efficiency. The optimal conditions achieving 78.57% turbidity reduction were a pH of 8.5, a coagulant dosage of 100 mL/L, and a settling time of 120 min. These findings highlight the significant potential of Pine cone extract as an effective, sustainable, and eco-friendly organic coagulant for raw water treatment. Full article
(This article belongs to the Section Wastewater Treatment and Reuse)
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24 pages, 2822 KiB  
Review
Green Pathways: Enhancing Amine Synthesis Using Deep Eutectic Solvents
by Andrés R. Alcántara and Gonzalo de Gonzalo
Catalysts 2025, 15(6), 586; https://doi.org/10.3390/catal15060586 - 12 Jun 2025
Viewed by 3021
Abstract
Deep eutectic solvents (DESs) have emerged as prominent, environmentally benign substitutes for traditional solvents and catalysts in organic synthesis, notably in the synthesis of amines, pivotal structures in many industrial sectors. Their distinctive physicochemical attributes—including negligible volatility, exceptional thermal stability, and adjustable polarity—render [...] Read more.
Deep eutectic solvents (DESs) have emerged as prominent, environmentally benign substitutes for traditional solvents and catalysts in organic synthesis, notably in the synthesis of amines, pivotal structures in many industrial sectors. Their distinctive physicochemical attributes—including negligible volatility, exceptional thermal stability, and adjustable polarity—render them particularly advantageous for facilitating a broad spectrum of amination reactions. DESs can serve dually as reaction media and as intrinsic catalytic systems, accelerating reaction kinetics without necessitating supplementary catalysts or severe reaction conditions. They are especially efficacious in processes such as reductive amination, transamination, and multicomponent transformations, often affording superior yields and streamlining product isolation. The extensive hydrogen-bonding network intrinsic to DESs is believed to mediate crucial mechanistic steps, frequently obviating the requirement for external additives. Moreover, DESs are recyclable and exhibit compatibility with a diverse array of substrates, encompassing bio-derived and pharmaceutical intermediates. Full article
(This article belongs to the Special Issue Feature Papers in Catalysis for Pharmaceuticals)
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