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This study explores the utilization of bio-polyol, derived from castor oil modified with waste tire rubber (WTR), in the synthesis of rigid polyurethane-polyisocyanurate foams. Two WTR concentrations (10% and 20%) were incorporated, investigating their impact on foaming, cellular structure, and various foam properties. Response surface methodology assessed the influence of polyol/isocyanate ratios and WTR content on thermal, physical, and mechanical responses. Results indicated significant effects of polyol/isocyanate ratios on thermal and density properties, while WTR content exhibited an opposite trend. Mechanical behavior showed a distinct pattern compared to thermal and physical aspects, suggesting no conclusive correlation between compressive stress variability and polyol/ isocyanate ratio or WTR content. Consequently, the application of these foams depends on specific property requirements, highlighting the potential of sustainable bio-polyols and recycled WTR in replacing conventional petroleum-based counterparts in polyurethane foam production. Highlights * Development of rigid polyurethane-polyisocyanurate foams based on castor oil. * Polyurethane-polyisocyanurate foams modified with waste tire rubber. * Increased isocyanate index impacts thermal stability and density. * Response surface methodology showed variability in compressive stress behavior and the polyol/isocyanate ratio. * For application of polyurethane-polyisocyanurate foams will depend on the desired properties. KEYWORDS castor oil, response surface methodology, rigid polyurethane-polyisocyanurate foams, tire rubber waste, 1 | INTRODUCTION Improper disposal of solid waste is one of the main environmental problems currently faced. (1) With the increase in population and consumption, the amount of waste generated [...]

[Display omitted] Improving ligand-to-active metal charge transfer (LAMCT) by finely tuning the organic ligand is a decisive strategy to enhance charge transfer in metal organic frameworks (MOFs)-based catalysts. However, in most MOFs loaded with active metal catalysts, electron transmission encounters massive obstacle at the interface between the two constituents owing to poor LAMCT. Herein, amines (–NH 2) functionalized MOFs (NH 2 -MIL-101(Cr)) encapsulated active metal Pt nanoclusters (NCs) catalysts are synthesized by the polyol reduction method and utilized for the photoreduction of CO 2. Surprisingly, the introduction of –NH 2 (electron donating) groups within the matrix of MIL-101(Cr) improved the electron migration through the LAMCT process, fostering a synergistic interaction with Pt. The combined experimental analysis exposed the high number of metallic Pt (Pt0) in Pt@NH 2 -MIL-101(Cr) catalyst through seamless electron shuttling from N of –NH 2 group to excited Pt generating versatile hybrid Pt-N catalytic centres. Consequently, these versatile hybrid catalytic centres act as electro-nucleophilic centres, which enable the efficient and selective conversion of C O bond in CO 2 to harvest CH 4 (131.0 µmol.g−1) and maintain excellent stability and selectivity for consecutive five rounds, superior to Pt@MIL-101(Cr) and most reported catalysts. Our study verified that the precise tuning of organic ligands in MOFs immensely improves the surface-active centres, electron migration, and catalytic selectivity of the excited Pt NCs catalysts encaged inside MOFs through an improved LAMCT pathway. [ABSTRACT FROM AUTHOR]

A polyol bonding agent (BA) was utilized to enhance the mechanical properties of propellant with low aluminum content. Through scanning electron microscope (SEM) and X‐ray photoelectron spectroscopy (XPS) analysis, it was discovered that BA can physically bond to the surfaces of ammonium perchlorate (AP) and hexogen (RDX). The results of mechanical testing showed that the use of BA can significantly improve the mechanical properties of propellants. Specifically, as the amount of BA increases, the maximum tensile strength (σm) of the propellant also increases, the fracture elongation (εb) initially increases and then decreases, the "dewetting ratio" continuously decreases, and the creep resistance of the propellant also increases. At a BA content of 0.2%, the σm of the propellant reaches 0.6 MPa, the εb exceeds 50%, and the "dewetting ratio" is less than 1.1. [ABSTRACT FROM AUTHOR]

In this work, ruthenium-based catalysts were synthesized via polyol reduction method with different metal oxides as support and caesium as promoter. The samples were characterized through XRD, ICP-OES, nitrogen physisorption and XPS. Then, the catalysts were tested for ammonia synthesis in the range of temperatures 548–673 K and pressures 1–5 MPa. The synthesized catalysts allowed an ammonia production rate approximately four times higher compared with the performances of similar catalytic formulations in literature (tested at same conditions). The best performance were achieved with the Cs–Ru/CeO 2 (1% wt Cs, 5% wt Ru), reaching an ammonia production of nearly 73 mmol h−1∙g cat −1 at 673 K and 5 MPa. As showed by the XPS analysis, the increased Ce3+/Ce4+ ratio led to an enhancement of oxygen vacancies, which favoured the dissociative adsorption of nitrogen, that is the limiting step in the ammonia synthesis reaction. Such high catalytic activity can be ascribed to the beneficial effect of the polyol reduction method for the maximization of the exposure of active sites. [Display omitted] • Ru-catalysts were synthesized via polyol reduction and tested for NH 3 production. • Cs–Ru/CeO 2 enabled a NH 3 production rate of 43 mmol h−1∙g cat −1 at 673 K and 1 MPa. • Increased Ce3+/Ce4+ ratio enhanced oxygen vacancies favouring N 2 adsorption. [ABSTRACT FROM AUTHOR]

The goal of this work was to evaluate the chemical constitution and health-promoting potential of 12 varieties of Chaenomeles × superba, speciosa and japonica leaves. Carotenoids, chlorophylls, triterpenes, sugars, polyols and acids were analyzed quantitatively and qualitatively using high pressure liquid chromatography (LC) coupled with mass spectrometry (MS), while the mineral profile was determined using atomic absorption spectroscopy (AAS). Moreover, the in vitro anticholinergic potential (inhibition of acetyl-cholinesterase (AChE) and butyryl-cholinesterase (BuChE)) and antioxidant (ABTS, FRAP, ORAC) capacity were evaluated. For the first time in Chaenomeles genotypes 26 carotenoid derivatives and 22 chlorophyll derivatives were identified. Some varieties contained high amounts of carotenoids and chlorophylls (Ch. × superba 'Colour Trail', 'Nicoline', 'Pink Lady', 'Texas Scarlet'), and triterpenes (Ch. speciosa 'Simonii', 'Rubra', and Ch. × superba 'Colour Trail', 'Nicoline') and showed high ORAC antioxidant (Ch. × superba 'Pink Lady' and Ch. speciosa 'Simonii') and anticholinergic (Ch. speciosa species) activity. The studied leaves also contained sugars (3.1 to 16.5 mg/100 g), organic acids (3.9–8.1 g/100 g), and minerals (Ca, Cu, Fe, K, Mg, Mn, Na, and Zn). In conclusion, Chaenomeles leaves show potential as a new source for the production of nutraceuticals, as well as for medical and/or cosmetic purposes. [ABSTRACT FROM AUTHOR]

Cryopreservation is a common way for long‐term storage of therapeutical proteins, erythrocytes, and mammalian cells. For cryoprotection of these biosamples to keep their structural integrity and biological activities, it is essential to incorporate highly efficient cryoprotectants. Currently, permeable small molecular cryoprotectants such as glycerol and dimethyl sulfoxide dominate in cryostorage applications, but they are harmful to cells and human health. As acting in the extracellular space, membrane‐impermeable macromolecular cryoprotectants, which exert remarkable membrane stabilization against cryo‐injury and are easily removed post‐thaw, are promising candidates with biocompatibility and feasibility. Water‐soluble hydroxyl‐containing polymers such as poly(vinyl alcohol) and polyol‐based polymers are potent ice recrystallization inhibitors, while polyampholytes, polyzwitterions, and bio‐inspired (glyco)polypeptides can significantly increase post‐thaw recovery with reduced membrane damages. In this review, the synthetic macromolecular cryoprotectants are systematically summarized based on their synthesis routes, practical utilities, and cryoprotective mechanisms. It provides a valuable insight in development of highly efficient macromolecular cryoprotectants with valid ice recrystallization inhibition activity for highly efficient and safe cryopreservation of cells. [ABSTRACT FROM AUTHOR]

BACKGROUND: Development of insecticide resistance in the major malaria vectors has necessitated the development of novel vector control tools. One such strategy involves the use of toxic sugar baits that targets the sugar‐feeding behaviour of mosquito vectors. In this study, we investigated the potential of polyols, as a toxic food (sugar) source in toxic sugar baits against the malaria vector Anopheles stephensi Liston. We examined the acute toxicity of six polyols, namely, erythritol, glycerol, mannitol, propylene glycol (PG), sorbitol, and xylitol on adult female An. stephensi mosquitoes at two different concentrations – 2% and 10%. We also studied changes in fecundity, egg hatchability and mid‐gut peroxide levels induced by polyol exposure. RESULTS: Among the six polyol compounds tested, PG was most toxic and lethal followed by glycerol and erythritol (P < 0.001) compared to the control (sucrose). PG induced acute mortality at different tested concentrations. In the erythritol‐ and glycerol‐fed groups, a dose‐dependent effect on mortality was observed. Glycerol evidently reduced fecundity and egg‐hatchability in gonotrophic cycles G1 and G2. Sucrose was the preferred food source (48%), followed by erythritol (18%), PG (10%) and glycerol (8%). Ingestion of polyols increased peroxide levels in mosquito guts, which persisted for extended durations ultimately resulting in rapid mortality (P < 0.05). CONCLUSION: The present study highlights the usefulness of sugar polyols for the development of toxic sugar baits with minimal yet effective ingredients. Further research could be focused on field experiments and on the exploration of synergistic effects of different polyols for optimization of field applications. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

For the first time, oxide (TiO2, CeO2, ZnO, Al2O3) supported Cu catalysts, prepared by the aqueous reduction method using sodium borohydride, were employed for the acceptorless dehydrogenation of 2‐octanol and various C4–C8 polyols. The method used to prepare the catalysts enabled the formation of small Cu particles in the range of 14–36 nm, depending on the point of the zero charge of the support. We showed that the conversion increased with Cu surface area, where Cu/TiO2 led to the highest conversion of 2‐octanol (>99.9%). The selectivity depends on the support and conversion. Up to 80% conversion, the selectivity to 2‐octanone was between 83% and 90% when using Cu/TiO2. In this study, we also report for the first time the acceptorless dehydrogenation of 1,3‐butanediol, 2,3‐butanediol, 1,2‐pentanediol, and 1,5‐pentanediol in liquid phase. While metal active sites promoted the dehydrogenation reaction, the presence of acidic and basic sites favored the formation of by‐products, mainly resulting from dehydration reactions, pinacol rearrangements, and aldol and retro‐aldol condensations. In addition to value‐added chemicals, all the reactions also released molecular hydrogen. [ABSTRACT FROM AUTHOR]

During the last decades, the interest in the development of materials fully or partially biobased has increased. Polyurethanes are extensively used in a wide range of industries because of their versatility. The present work explores the synthesis of partially biobased poly(urethane‐urea) (PUU) composites employing soy‐based polyol (SPO) and cellulose nanocrystals (CNC). The latter were incorporated during the synthesis (in‐situ) or after the synthesis (ex‐situ). The possibility of a technological application as coatings was investigated for the designed materials. Polycaprolactone diol was used as a soft segment due to high functionality of the soy‐based polyol. The physicochemical, thermal and mechanical properties of the prepared matrices were analyzed. Poly(urethane‐urea)s containing up to 20% by weight of biobased polyol showed coating application potentiality. Compared to a polycaprolactone‐based polyurethane, the utilization of the bioprecursor enhanced light absorption in the UV–Vis region. In addition, partially biobased systems showed better mechanical resistance (Young's modulus increased up to 6 times) and hydrophobicity (sweeling decreased from 60 to 8 per cent by weight). Incorporation of cellulose nanocrystals affected primarily the physicochemical and rheological properties of dispersions. Regarding coating properties, nanocrystals utilization complemented the soy‐based polyol improving the performance of the films. Furthermore, the incorporation route affected the dispersions and films properties. Highlights: SPO was incorporated up to 20 per cent by weight in PUU composites.Higher SPO contents improved UV–Vis absorption and tensile strength of films.Films were less hydrophilic as more SPO was incorporated.The CNC‐reinforcement was complementary to the utilization of the SPO.CNC incorporation route affects properties and performance of the coatings. [ABSTRACT FROM AUTHOR]

Polyurethane is a kind of synthetic polymer composed of isocyanates, polyols and chain extenders. Due to its excellent mechanical flexibility, biodegradability and physicochemical properties, polyurethane is widely used in biological, medical, food and antifouling fields. With the continuous development of science and technology, ordinary polyurethane materials have been unable to meet people's diverse and high standard aseptic requirements, and the development and application of antibacterial polyurethane is getting more and more attention. In this paper, the antibacterial modification methods of polyurethane materials were introduced, and the application status and antibacterial mechanism of polyurethane materials in medical treatment, food packaging, water treatment and other aspects in recent years were reviewed. At the end, the problems faced in the application of antibacterial polyurethane materials and corresponding improvement measures are discussed. [ABSTRACT FROM AUTHOR]

High internal phase emulsions (HIPEs) are commonly stabilized by a large amount of surfactants that should be removed after the polymerization of the continuous phase, and the resulting polyHIPEs from W/O HIPEs are usually brittle and chalky. Herein we report on an amphiphilic polymerizable polyurethane (PPU) macromolecular surfactant synthesized by polyaddition reaction of diisocyanates and polyols, which can well stabilize up to 88% internal phase volume of W/O HIPE with a content of only 5 wt% based the oil phase. Compared with the HIPEs stabilized by traditional surfactant Span 80, HIPEs stabilized by PPU at either room temperature or 70 °C are much more stable owing to the increased viscosity which can inhibit droplet coalescence. Moreover, the resulting polyHIPEs not only have several times higher mechanical properties than those stabilized by Span 80 but also have higher elasticity. The effects of concentration of PPU on the morphology and mechanical properties of the resulting polyHIPEs were investigated. It was found that with the increase of PPU content, the average void and window sizes decreased, while the compression strength increased. Cyclic compression tests were performed to examine reversible compressibility and durability of these polyHIPEs. The polymerizable polyurethane macromolecular surfactant (PPU) synthesized through the polyaddition reaction of diisocyanates and polyols can solely stabilize high internal phase emulsions (HIPEs), and highly interconnected macroporous polymer produced by the polymerization of HIPE stabilized with PPU, known as polyHIPE, can withstand large deformation compression with no visible cracks. [ABSTRACT FROM AUTHOR]

Purpose: This study aims to fabricate the acrylic-based polymeric composite coating with a hydrophobic surface associated with natural oil polyol (NOP) and polydimethylsiloxane with the incorporation of 3 Wt.% SiO2 nanoparticle (SiO2np) against the corrosive NaCl media. Design/methodology/approach: The structural properties of the formulated polymeric composite coatings were investigated by using Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, water contact angle (WCA) and cross-hatch (X-Hatch) tests. The WCA measurement was used to study the surface wettability of the formulated polymeric composite coatings. The corrosion protection performance of the nanocomposite coated on the mild steel substrate was studied by immersing the samples in 3.5 Wt.% NaCl solution for 30 days using electrochemical impedance spectroscopy. Findings: The enhanced polymeric composite coating system performed with an excellent increase in the WCA up to 111.1° which is good hydrophobic nature and very high coating resistance in the range of 1010 Ω attributed to the superiority of SiO2np. Originality/value: The incorporation of SiO2np into the polymeric coating could enhance the surface roughness and hydrophobic properties that could increase corrosion protection. This approach is a novel attempt of using NOP along with the addition of SiO2np. [ABSTRACT FROM AUTHOR]

Environmental issues, including climate change and plastic pollution, have compelled scientists to look at alternatives to traditional polymers. Scientists are actively researching biobased hyperbranched polymers, an emerging group of highly branched polymers made from sustainable resources. They are seen as a promising alternative to petrochemical-based polymers. Hyperbranched polymers can be made using single- and double-monomer techniques. This review provides an extensive perspective of the synthesis and properties of biobased hyperbranched polymers made from a variety of renewable starting materials, including starch, lignin, vanillin, levulinic acid, furfurylamine, ferulic acid, citric acid, adipic acid, succinic acid, and tannic acid and various vegetable oils have been investigated till date. Most of these biobased hyperbranched polymers have been created using vegetable oil as their raw materials because numerous vegetable oil derivatives like monoglycerides, polyols, and fatty acids can be potentially used as monomers for the polymer. In the paper, specifics about modified biobased hyperbranched polymers, their composites, nanocomposites, and functionalized versions are highlighted. These materials belong to a class that combines the special characteristics of hyperbranched polymers with the reinforcing and functionalizing effects of fillers like silver, carbon, silicone, clay, etc. Lastly, the paper also discusses the various practical applications of biobased hyperbranched polymers in various industrial sectors and their prospects for the future. [ABSTRACT FROM AUTHOR]

Polyurethanes are the result of a reaction between an isocyanate and a polyol. The large variety of possible reagents creates many possible polyurethanes to be made, such as soft foams, rigid foams, coatings, and adhesives. This polymer is one of the most produced and consumed polymers in the world with an ever-increasing demand. Despite its usual petrochemical nature, research on bio-based polyurethanes flourishes due to the ease in creating bio-based polyols. This work covers the synthesis of a novel macauba kernel oil polyol by the epoxidation of the oil, followed by a ring-opening reaction of the epoxide with glycerol, used for the preparation of polyurethane foams using different NCO/OH ratios. The FTIR and H1 results confirm the formation of the epoxide and polyol, and the polymers in all NCO/OH ratios were confirmed by FTIR, showing great similarities between the samples, especially PU 1.0 and PU 1.2. Despite the TGs showing close behaviors for the three samples, their DTGs showed great difference between the samples, with PU 1.0 presenting a regular PU DTG profile with three degradation peaks while the other two sample presented five degradation peaks, indicating a higher crosslinking density in them. [ABSTRACT FROM AUTHOR]

Friction remains as the primary mode of energy dissipation and components wear, and achieving superlubricity shows high promise in energy conservation and lifetime wear protection. The results in this work demonstrate that direct superlubricity combined with superlow wear can be realized for steel/Si3N4 contacts on engineering scale when polyhydroxy alcohol solution was selectively modified by amino group. Macroscopic direct superlubricity occurs because 3-amino-1,2-propanediol molecules at the friction interface could be induced to rotate and adsorb vertically on the friction surface, forming in-situ thick and dense molecular films to passivate the asperity contacts. Furthermore, amino modification is also conducive to improving the lubrication state from boundary to mixed lubrication regime by strengthening the intermolecular hydrogen bonding interaction, presenting enhanced load-bearing capability and reduced direct solid asperity contacts. Thus, direct superlow average friction of 0.01 combined with superlow wear are achieved simultaneously. The design principle of direct superlubricity and superlow wear in this work indeed offers an effective strategy to fundamentally improve energy efficiency and provide lifetime wear protection for moving mechanical assemblies. [ABSTRACT FROM AUTHOR]

SUMMARY: In eggs, the albumen and yolk undergo physicochemical changes during storage, which will decrease egg quality. Several factors can contribute to the loss of egg quality (such as temperature, humidity, duration of storage, thin eggshell, age of the flock). Coatings are a tool that can help maintain egg quality during long storage periods. The standard composition of egg coatings includes polysaccharides, lipids, proteins and polyols that can be used as plasticising substances and incorporated to induce flexibility in films. Glycerol is the most commonly used plasticiser in egg coatings due to its abundance and relatively low cost. However, other substances have demonstrated better results when added to coatings to extend the shelf life of eggs. Few studies have investigated the relationship between polyol plasticisers and the different bases for preparing coatings. Furthermore, little discussion exists about which levels should be incorporated into the egg-coating solution. The real impact of using polyols in egg coatings still has some gaps. This review gives an overview of the current use of polyols and trends in developing new egg coatings. [ABSTRACT FROM AUTHOR]

Traditional adhesives made using urea or phenol formaldehyde are toxic to humans and the environment, and as a result, the industry is very interested in developing bio‐based adhesives. Polyurethane (PU)‐based adhesives are very attractive due to their strong bonding strength, and thermal and chemical stability. Polyols derived from petrochemicals are one of the most important constituents in PU‐based adhesives. Current trends are to find an alternative for petrochemical‐based polyols without compromising the important characteristics of adhesives. In this research, PU adhesives were prepared using soybean oil‐based polyol and isocyanate. Three different diols such as 1,2‐ethanediol (EDO), 1,4‐butanediol (BDO), and 1,6‐hexanediol (HDO) were used to study the effect of crosslinking, amount of crosslinkers (diols), and diol's chain length on the properties of bio‐based adhesives. The adhesive's lap shear strength using metallic and wood coupons was measured. The BDO‐based bio‐adhesives showed the best bonding strength compared to EDO and HDO adhesives. The mechanical strength was observed to be increasing with an increase in the amount of diols up to a certain concentration and then started decreasing. On the oakwood, the bonding strength was increased from 3 to 6.36 MPa after incorporating 10 wt% of BDO which was the highest bonding strength observed among all the other adhesives. The thermal and chemical stability of these adhesives were also studied. Structural characterization confirms no significant changes after being immersed in different solvents for 24 h. This work introduces a sustainable alternative to petroleum‐based adhesives using polyols from vegetable oil. Highlights: Soybean oil‐based polyol was used for adhesives.1,2‐Ethanediol, 1,4‐butanediol, and 1,6‐hexanediol were used as crosslinkers.The bonding strength was measured using wood and metallic coupons.The bonding strength was observed to be increasing with an increase in the amount of diols.The highest bonding strength of 6.36 MPa was observed. [ABSTRACT FROM AUTHOR]

Vegetable-oil-based polyurethane has become a promising sustainable candidate for controlled-release fertilizer based on green chemistry. The purpose of this study was to prepare a series of coatings from selective feedstocks including five vegetable oils with a high saturation degree, mono-unsaturation degree, or poly-unsaturation degree, considering that vegetable oil fatty acids played a key role in the synthesis of polyol and polyurethane. The effect of the type and proportion of fatty acids on the physicochemical properties, microstructure, and macro-properties of vegetable-oil-derived polyols and their resulting coatings was characterized and discussed. The position and number of the hydroxy groups were determined by the type and proportion of fatty acid, and polyol from linseed oil with a high poly-unsaturation degree and three carbon–carbon double bonds had a high hydroxyl value and functionality, whereas polyol from palm oil with a high saturation degree possessed the lowest hydroxyl value and functionality. The resultant coating from linseed-oil-based polyol had a good cross-linking density, and the nitrogen release longevity of coated urea was 56 days at a coating percentage of 3%, and its nitrogen use efficiency was increased by 27.15% compared with conventional urea. Although the palm-oil-based coating had good hydrophobicity, its coated urea was not ideal. Overall, this study has enriched theories of bio-based polyurethane coatings for controlled-release fertilizers; using vegetable oil with a poly-unsaturation degree, it is easy to obtain an excellent coating for controlled-release fertilizer, and this will help provide economic and environmental benefits. [ABSTRACT FROM AUTHOR]

The document is a contents list of the journal "Dalton Transactions: An International Journal of Inorganic Chemistry," which covers various topics related to inorganic chemistry. It includes articles on metal complexes, electrocatalysts, nanocrystals, and organic synthesis. The journal aims to provide original research and perspectives to contribute to scientific progress in the field of chemistry. One article discussed in the document is about the synthesis and characterization of copper complexes that can be used in the degradation of organic dyes using visible light. Another article focuses on the synthesis and characterization of palladium complexes for use in focused electron beam induced deposition. [Extracted from the article]

The field of 2D nanomaterials is ever-growing with a myriad of synthetic advancements that have been used to obtain such materials. There are top-down, as well as bottom-up, fabrication methods for obtaining 2D nanomaterials; however, synthesis of 2D nanomaterials from solution offers a simple scalable way to control size, shape, and surface. This review outlines the recent advances in colloidal polyol synthesis of 2D nanomaterials and provides perspectives on the similarities and differences in various syntheses. Various materials classes are presented and discussed, including metals, oxides, chalcogenides, and halides, that can be synthesized as 2D nanomaterials via a polyol process. Throughout the literature, polyol media is demonstrated to be versatile not only as a solvent and reducing agent for metal precursors but also as a binding and shape-directing agent for many 2D nanomaterials. Polyols also offer the ability to dissolve various surfactants and additives that can further control the morphology and composition of various nanomaterials. In this review, we outline the various 2D materials that have been realized via the solution polyol route. [ABSTRACT FROM AUTHOR]

The document is a contents list for the journal "Green Chemistry," published by The Royal Society of Chemistry. It highlights the articles and papers featured in the current issue, covering a range of topics related to sustainable chemistry and green technologies. The articles include research on bio-based polymers, nitrogen fixation strategies, carbon aerogels for energy storage, and the use of ionic liquids in new energy and biotechnologies. The journal aims to provide cutting-edge research for a greener and more sustainable future. [Extracted from the article]

Following our previous studies aimed at the valorization of cellulose waste and glycerol, biobased polyols-polyesters were synthesized using both a "green approach" and a novel heterogeneous catalyst based on scandium silicate thortveitite. The latter showed an enhanced linear selectivity compared with most of the analogous catalysts reported in recent studies. Polymers obtained were tested in two important reactions with potential industrial applications: as co-monomers for the synthesis of polyurethanes and as binders for 3D printers. The polyols-polyesters were obtained, with the average molecular weight ranging from 440 to 1050 Da. It is worth noting that the typical polyol polyester used in coatings is branched and has an average molecular weight of 2000–4000 Da. [ABSTRACT FROM AUTHOR]

With the implementation of the "plastic restriction order" and the demand for sustainable society development, biodegradable coatings derived from biomass materials have garnered significant interest. This study presents the synthesis of a double‐salt bio‐based waterborne polyurethane (PLA‐WPU) by utilizing poly(lactic acid) polyol (PLA) and isophorone diisocyanate (IPDI) as the main raw materials, along with 2,2‐dihydroxymethylpropionic acid (DMPA) and sodium ethylenediamine ethanesulfonate (A‐95) as a hydrophilic chain extender. Synergistic reinforcement of PLA‐WPU using hydrophobically modified cellulose nanocrystals (M‐CNC) and polycarbonate diimide (PDCDA). At an M‐CNC content of 3% relative to the effective mass of PLA‐WPU, the tensile strength reached 36.12 MPa. After 8 days a lipase PBS solution, the degradation rate reached 54%. Excellent waterproof performance was observed, exhibiting a contact angle of 143.5°. When applied as a surface coating on kraft paper, the Cobb 60 value decreased from 74.0 to 28.6 g/m2, while increasing the tensile strength by 451.3%. Importantly, the kraft paper maintained excellent waterproofing, mechanical strength, and high barrier properties even after repeated folding, high and low‐temperature conditions, and exposure to varying pH solutions. It proved to be both degradable and recyclable, making it a promising alternative to liner paper or plastic membrane, especially in food packaging. [ABSTRACT FROM AUTHOR]

This study explored the feasibility of Waste Cooking Oil (WCO)‐based Bio‐Polyurethane (Bio‐PU) as an eco‐friendly alternative to petroleum‐derived polyols in plywood adhesives. The objective is to evaluate the impact of varied WCO concentrations and methylene diphenyl diisocyanate (MDI) levels on Bio‐PU and plywood performance. The Bio‐PU's characteristics, rheology, and functional groups are studied. Plywood made from three layers of 100 mm x 100 mm × 2 mm rubberwood (Hevea brasiliensis) veneer is bonded with Bio‐PU using a dual spread approach at 180 g.m−2, hot pressed at 120 °C and 1 MPa for 4 min. The laboratory‐fabricated plywood is tested for physical, mechanical, and adhesive properties. Results showed that Bio‐PU exhibited unique adhesive characteristics, with excellent adhesive strength, despite a slight decrease with higher WCO concentrations. WCO insertion do not compromise delamination resistance. FTIR analysis confirmed successful polyurethane chain synthesis. This research highlighted the potential of WCO‐based Bio‐PU's as a sustainable, high‐performance plywood adhesive. [ABSTRACT FROM AUTHOR]

Polyurethane foams are materials characterized by low density and thermal conductivity and can therefore be used as thermal insulation materials. They are synthesized from toxic and environmentally unfriendly petrochemicals called isocyanates and polyols, which react with each other to form a urethane group via the displacement of the movable hydrogen atom of the −OH group of the alcohol to the nitrogen atom of the isocyanate group. The following work describes the synthesis of polyurethane foams, focusing on using environmentally friendly materials, such as polyols derived from plant sources or modifiers, to strengthen the foam interface derived from plant precipitation containing cellulose derived from paper waste. The polyurethane foam industry is looking for new sources of materials to replace the currently used petrochemical products. The solutions described are proving to be an innovative and promising area capable of changing the face of current PU foam synthesis. [ABSTRACT FROM AUTHOR]

Stabilized enzymes are crucial for the industrial application of biocatalysis due to their enhanced operational stability, which leads to prolonged enzyme activity, cost-efficiency and consequently scalability of biocatalytic processes. Over the past decade, numerous studies have demonstrated that deep eutectic solvents (DES) are excellent enzyme stabilizers. However, the search for an optimal DES has primarily relied on trial-and-error methods, lacking systematic exploration of DES structure-activity relationships. Therefore, this study aims to rationally design DES to stabilize various dehydrogenases through extensive experimental screening, followed by the development of a straightforward and reliable mathematical model to predict the efficacy of DES in enzyme stabilization. A total of 28 DES were tested for their ability to stabilize three dehydrogenases at 30°C: (S)-alcohol dehydrogenase from Rhodococcus ruber (ADH-A), (R)-alcohol dehydrogenase from Lactobacillus kefir (Lk-ADH) and glucose dehydrogenase from Bacillus megaterium (GDH). The residual activity of these enzymes in the presence of DES was quantified using first-order kinetic models. The screening revealed that DES based on polyols serve as promising stabilizing environments for the three tested dehydrogenases, particularly for the enzymes Lk-ADH and GDH, which are intrinsically unstable in aqueous environments. In glycerol-based DES, increases in enzyme half-life of up to 175-fold for Lk-ADH and 60-fold for GDH were observed compared to reference buffers. Furthermore, to establish the relationship between the enzyme inactivation rate constants and DES descriptors generated by the Conductor-like Screening Model for Real Solvents, artificial neural network models were developed. The models for ADH-A and GDH showed high efficiency and reliability (R² > 0.75) for in silico screening of the enzyme inactivation rate constants based on DES descriptors. In conclusion, these results highlight the significant potential of the integrated experimental and in silico approach for the rational design of DES tailored to stabilize enzymes. [ABSTRACT FROM AUTHOR]

Bio-based polyurethane foam sorbents were developed, incorporating different amounts of rice husk ash, 2, 8 and 20 wt% relative to the total mass of the polyols for the adsorption of diesel oil in single-phase and two-phase systems. The composites were characterized using scanning electron microscopy, microtomography, X-ray diffraction, infrared spectroscopy, thermogravimetry analysis and contact angle. In single-phase diesel oil systems, higher levels of ash incorporation (8 and 20%) increased the hydrocarbon removal capacity by up to 43% compared to pure polyurethane foam. Removals of up to 5.348 mg g−1 were found for the composite with 8% ash and 5.518 mg g−1 for the composite with 20%. In two-phase systems, varying the concentration of diesel oil from 10 g L−1 to 150 g L−1, there is a possibility that the lower contact angle of the composites may interfere with adsorption, as the composite with 2% ash tended to have a higher diesel oil sorption capacity. Sorption kinetics showed a high rate at contact times of around 8 min. The non-linear pseudo-second-order models fitted the observed sorption phenomena satisfactorily, with coefficients of determination greater than 0.90. [ABSTRACT FROM AUTHOR]

Vat photopolymerization 3D printing has proven very successful for the rapid additive manufacturing (AM) of polymeric parts at high resolution. However, the range of materials that can be printed and their resulting properties remains narrow. Herein, we report the successful AM of a series of poly(carbonate‐b‐ester‐b‐carbonate) elastomers, derived from carbon dioxide and bio‐derived ϵ‐decalactone. By employing a highly active and selective Co(II)Mg(II) polymerization catalyst, an ABA triblock copolymer (Mn=6.3 kg mol−1, ÐM=1.26) was synthesized, formulated into resins which were 3D printed using digital light processing (DLP) and a thiol‐ene‐based crosslinking system. A series of elastomeric and degradable thermosets were produced, with varying thiol cross‐linker length and poly(ethylene glycol) content, to produce complex triply periodic geometries at high resolution. Thermomechanical characterization of the materials reveals printing‐induced microphase separation and tunable hydrophilicity. These findings highlight how utilizing DLP can produce sustainable materials from low molar mass polyols quickly and at high resolution. The 3D printing of these functional materials may help to expedite the production of sustainable plastics and elastomers with potential to replace conventional petrochemical‐based options. [ABSTRACT FROM AUTHOR]

The utilization of leather waste (LW) in a polyurethane (PU) matrix makes a smart and novel shape stable phase change material (SSPCM). This is essential for sustainability as it reduces landfill waste after use. The PU is synthesized in bulk with a 90% yield, using biodegradable polycaprolactone diol and bio‐based polyol (castor oil), along with tolylene‐2,4‐diisocyanate. PL and PLG composites are prepared by blending of constituent components PU (P), LW (L), and poly(glycidyl methacrylate) (PGMA, G), as specified by their code names. Role of LW (hydrogen bonding and chemical crosslinking) and morphology are elucidated by FTIR and SEM, respectively. Self‐healing time (2 h), shape fixity ratios (Rf) (PL: 60–80% and PLG: 60–70%) and shape recovery ratios (Rr) (100% for both) are determined at 60°C. PLG displays faster shape recovery in water (<30 s) compared to air (>300 s). Shape stability and thermal properties of the SSPCM are examined using the temperature responsive leakage study, TGA, and DSC. This research introduces a new approach for using leather waste (LW) in SSPCM, with self‐healing and 100% Rr. This material may find application where SSPCM with high durability and flexibility is essential such as textile and footwear materials. [ABSTRACT FROM AUTHOR]

The bio‐based hydrophilic monoglycerol succinate was synthesized and reacted with bio‐based raw materials including polyols, pentamethylene diisocyanate, 1,4‐butanediol, to prepare the waterborne polyurethane acrylate (Bio‐WPUA) emulsions with high bio‐based content. The effect of bio‐based polyol categories including poly(trimethylene ether glycol), poly(tetrahydrofuran), and castor oil on the properties of Bio‐WPUA and its films were studied. The structure, thermal stability, crystallinity, contact angle, and mechanical properties of Bio‐WPUA film were characterized with fourier infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry, X‐ray diffraction, contact angle analyzer, and mechanical tensile testing. It was found that Bio‐WPUA film containing poly(trimethylene ether glycol) as the soft‐segmented display good tensile stress, thermal stability, and water resistance with 1.38% of the water absorption rate, while Bio‐WPUA containing castor oil polyol as the soft‐segmented had good tensile strain and low‐temperature film‐forming properties with excellent film properties. The bio‐carbon content of Bio‐WPUA was high up to 40% according to ASTM D6866‐22, and possesses good physical mechanical and chemical resistance performance. The results provide theoretical guidance for the synthesis of polyurethane emulsions with bio‐based materials instead of petroleum‐based materials. [ABSTRACT FROM AUTHOR]

The research progress, existing problems and future development of flame retarding modification of bio-based polyurethane are summarized. The work summarized the research status of commonly used methods for preparing bio-based polyurethane, including basic characteristics, application effect and development prospect of various flame retardant agent. At present, vegetable oil-based polyols can effectively replace traditional industrial synthetic petroleum-based polyols as raw materials for the synthesis of bio-based polyurethane. However, there are still some shortcomings in this area that have not been addressed. The defects of polyurethane, such as flammability and smokiness, need to be improved. The practical application conversion rate of research results was not high. The environmental protection and safety performance of bio-based polyurethane can be further improved and enriched. Therefore, more efforts should be put into the above questions, which were all of great significance to the development of polyurethane. The research on retarding modification of polyurethane will have great development space and application value in the future. [ABSTRACT FROM AUTHOR]

Background: A diet low in fermentable oligo‐, di‐, monosaccharides and polyols (LFD) improves symptoms in patients with irritable bowel syndrome (IBS). Previous studies have focused on patients with IBS and diarrhea (IBS‐D). It is unclear whether LFD is effective for IBS with constipation (IBS‐C) or IBS with mixed bowel habits (IBS‐M). This open‐label, real‐world study evaluates the relative effectiveness of the LFD among IBS subtypes. Methods: This study analyzes data from a service that provides low‐FODMAP meals to individuals with IBS. Participants met with a registered dietitian and completed the IBS symptom severity survey (IBS‐SSS) before and after undergoing a 2–4‐week period of FODMAP restriction. The primary endpoint was the proportion of participants with ≥50‐point decrease in IBS‐SSS between the three IBS subtypes. Key Results: After FODMAP restriction, 90% of participants with IBS‐D, 75% with IBS‐C, and 84% with IBS‐M met the primary endpoint (p = 0.045). Similar improvement was seen for a 100‐point decrease, but the difference between IBS subtypes was not significant (p = 0.46). After FODMAP restriction, all groups had statistically significant improvement in total IBS‐SSS as well as individual symptom categories. Improvement in IBS‐SSS subcategories was similar among the groups except for the categories of bloating severity (IBS‐M had greatest improvement) and bowel movement satisfaction (IBS‐C had less improvement). Conclusion & Inferences: Though the proportion of responders was highest for IBS‐D and lowest for IBS‐C, the LFD led to robust improvement in overall symptoms in all IBS subtypes. Key individual symptoms also showed significant improvements in all IBS subtypes. [ABSTRACT FROM AUTHOR]

Polyalcohol liquefaction can be performed by acid or base catalysis, producing polyols with different properties. This study compared the mechanical properties of foams produced using polyols from liquefied Cytisus scoparius obtained by acid and base catalysis and using two different foam catalysts. The differences were monitored using FTIR analysis. Acid-catalyzed liquefaction yielded 95.1%, with the resultant polyol having an OH index of 1081 mg KOH/g, while base catalysis yielded 82.5%, with a similar OH index of 1070 mg KOH/g. Generally, compressive strength with dibutyltin dilaurate (DBTDL) ranged from 16 to 31 kPa (acid-liquefied polyol) and 12 to 21 kPa (base-liquefied polyol), while with stannous octoate (TIN), it ranged from 17 to 42 kPa (acid) and 29 to 68 kPa (base). Increasing water content generally decreased the compressive modulus and strength of the foams. Higher water content led to a higher absorption at 1670 cm−1 in the FTIR spectrum due to the formation of urea. Higher isocyanate indices generally improved compressive strength, but high amounts led to unreacted isocyanate that could be seen by a higher absorption at 2265 cm−1 and 3290 cm−1. DBTL was shown to be the best foam catalyst due to higher trimer conversion seen in the spectra by a higher absorption at 1410 cm−1. Acid- and base-derived polyols lead to different polyurethane foams with different FTIR spectra, particularly with a higher absorption at 1670 cm−1 for foams from acid-derived liquefaction. [ABSTRACT FROM AUTHOR]

Intensive research is currently being carried out worldwide to replace fossil raw materials with renewable ones or waste based on chemical synthesis. However, it is important that the newly developed raw materials do not conflict with global food production and recommend the use of non-edible or waste raw materials. Therefore, modified non-edible oilseed radish oil was used in the synthesis of polymeric materials. The functionalization of the oil was achieved through one-step, solvent-free transesterification process with triethanolamine, diethylene glycol, polypropylene glycol, ethylene glycol and propylene glycol. Biopolyols with hydroxyl numbers in the range of 237–346 mg KOH/g and different chemical structures were obtained. Open-cell polyurethane foams were produced by replacing 100% of the original petrochemical polyol with the biopolyols. The influence of the chemical structures of the biopolyols on the properties of the thermal insulation materials was analysed. The foams were characterised by low apparent densities of about 16 kg/m3. The type of biopolyol did not have a significant influence on the mechanical strength of the foams. A thermal analysis of the polyurethane biofoams was also carried out. [ABSTRACT FROM AUTHOR]

This paper discusses methods of using biomass from the agriculture, forestry, food and aquaculture industries as potential raw materials for bio-polyols and as fillers in the production of rigid polyurethane (RPUR) foams. Various aspects of obtaining bio-polyols are discussed, as well as the impact of replacing petrochemical polyols with bio-polyols on the properties of foams. Special attention is paid to the conversion of vegetable oils and lignin. Another important aspect of the research is the use of biomass as foam fillers. Chemical and physical modifications are discussed, and important factors, such as the type and origin of biomass, particle size and amount, affecting the foaming process, microstructure and properties of RPUR foams are identified. The advantages and disadvantages of using biomass in foam production are described. It is found that bio-polyols can replace (at least partially) petrochemical polyols while maintaining the high insulation and strength of foams. In the case of the use of biomass as fillers, it is found that the shaping of their properties is largely dependent on the specific characteristics of the filler particles. This requires further research into process optimization but allows for the fine-tuning of RPUR foam properties to meet specific requirements. [ABSTRACT FROM AUTHOR]

BACKGROUND: Polymeric microcapsules (MCs) have become an important issue and have attracted increasing attention because of their tunable physical and chemical properties. Diverse shell structures can confer multiple properties on MCs. RESULTS: Different polyols (1,4‐butanediol and glycerin) and polyamines (triethylenetetramine and isophorondiamine) were selected as crosslinkers to obtain emamectin benzoate (EB)‐loaded poly(urethane–urea) MCs (PU‐MCs) by interfacial polymerization. The four obtained PU‐MCs showed sphericity with different degrees of smoothness on their surfaces, and displayed a uniform size distribution ranging from 500 to 700 nm. Moreover, transmission electron microscopy showed that the shell thickness was roughly uniform, and was greatly influenced by the type and structure of the crosslinker. GI‐MCs, prepared using glycerin and isophorondiamine, had the largest shell thickness. GT‐MCs, obtained using glycerin and triethylenetetramine, had the highest encapsulation efficiency and drug‐loading content, and BT‐MCs, obtained using mixtures of 1,4‐butanediol and triethylenetetramine, had the fastest release behavior. Thermogravimetric analysis revealed that the greater the degree of shell crosslinking, the higher decomposition temperature and the greater the thermal stability. A BT‐MC suspension had the lowest viscosity and contact angle with the best wettability. Bioassay experiments showed that BT‐MCs exhibited good insecticidal activity against Plutella xylostella larvae with a half‐maximal lethal concentration of 4.19 mg/L. Furthermore, a BT‐MC suspension showed good thermal and light stability, with potential applications in minimizing the toxicity of EB through sustained release. CONCLUSION: Various properties of EB‐loaded PU‐MCs were modulated through simple selection of different polyols and polyamines during fabrication, which might have an important role in constructing the pesticide delivery system and improving pesticide utilization. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Cleansing products, particularly innovative cosmetic foams, must efficiently remove impurities with minimal impact on the skin barrier and have a favorable sensory profile. The choice of product ingredients is crucial to ensure the optimal characteristics. The current study aims to provide a comprehensive framework for understanding the variability in the characteristics of a cleansing foam to achieve desired properties. The novelty of this study lies in the combination of ingredients for their potential synergistic and complementary effects in cleansing dry skin, as well as the application of Quality by Design (QbD) elements to develop and optimize the formulation of cleansing foam. The effects of varying the concentration of mild surfactants, polyols, and gel-forming agents on the properties of the gels and of the generated foams were studied. Significant influences of the formulation factors were observed: an increased ratio of xanthan gum positively impacted the texture properties of the gel, whereas higher concentrations of surfactants had a negative impact on these parameters. Additionally, increasing the polyols ratio was found to negatively influence the foaming property and stability of the foam. The study established an optimal formulation of a cleansing foam with a ratio of 0.45% xanthan gum, 26.19% surfactants and 2.16% polyols to be used for dry skin hygiene. [ABSTRACT FROM AUTHOR]

Excessive sugar intake can lead to poor health outcomes. The use of sweeteners is considered as a strategy to reduce added sugar consumption. The presence of sweeteners in food products has increased significantly in many countries. Therefore, the aim of this study was to identify the added sugars and sweeteners in packaged products. 1550 (57.9%) out of 2676 food products contained at least one added sugar. Confectionery and desserts (35.38±24.82 g/100 g), and snack foods (20.70±16.20 g/100 g) were the main categories containing the highest amount of added sugar. 229 (8.6%) out of 2676 food products contained various types of sweeteners. The most popular added sugar was sucrose (62.9%), while the most popular sweetener was sorbitol (28.2%). This is the most comprehensive study in the city center of Edirne province in Türkiye reporting on the types and frequency of added sugars and sweeteners in packaged products. This study offers monitoring to improve the legislation of Türkiye on added sugars and sweeteners used in the food supply.

Abstract The study of diffusion in biological materials is crucial for fields like food science, engineering, and pharmaceuticals. Research that combines numerical and analytical methods is needed to better understand diffusive phenomena across various dimensions and under variable boundary conditions within food matrices. This study aims to bridge this gap by examining the diffusion of substances through biological materials analytically and numerically, calculating diffusivity and conducting surface analysis. The research proposes a process for sweetening Bing-type cherries (Prunus avium) using sucrose/xylitol solutions and a staining technique utilising erythrosine and red gardenia at varying concentrations (119, 238 and 357 ppm) and temperatures (40, 50 and 60 °C). Given the fruit's epidermis resistance, the effective diffusivities of skin were inferior to those in flesh. Temperature and concentration synergise in enhancing diffusion coefficients and dye penetration within the food matrix (357 ppm and 60 °C). Red gardenia displayed significant temperature-dependent variation (p = 0.001), whereas erythrosine dye remained stable by temperature changes (p > 0.05). Gardenia's effective diffusivities in cherry flesh and skin, at 357 ppm and 60 °C, 3.89E−08 and 6.61E−09 m2/s, respectively, significantly differed from those obtained at lower temperatures and concentrations. The results highlight the temperature-concentration impacts on mass transfer calculations for food colouring processes and preservation methodologies.

The aim of the work was to review modern extraction, detection and quantification analytical methods of inositols and their derivatives. Methods. Inositols are extracted from vegetable raw materials by methods of liquid extraction, under pressure, microwave extraction and supercritical fluid extraction. Quantitatively analyzed by methods of gas and liquid chromatography with preliminary derivatization. The structure of inositols can be determined by the NMR spectroscopy. Results. Inositols and their derivatives are biologically active compounds, wich are involved in the egulation of the intracellular calcium level, the transmission of hormonal signals, the breakdown of fats and the reduction of cholesterol in the blood, the modulation of the neurotransmitters activity, etc. Inositols are used in the production of vitamin preparations. The main source for inositols extraction is vegetable raw material, namely alfalfa, as well as wheat sprouts, grapefruit, hazelnuts and others. In the paper, the methods of inositols extraction with organic and inorganic solvents, including the use of a Soxhlet apparatus, liquid extraction under pressure, microwave extraction and supercritical fluid extraction are considered. The procedure of preliminary sample preparation and polyols derivatization for their further separation and quantitative determination is described. Modern chromatographic methods of polyols identification and quantitative determination are analyzed. The possibility of using 1H, 13C and 31P NMR spectroscopy to identify the structure of inositols and their derivatives is described. Conclusions. Inositols are biologically active compounds of a wide spectrum of action, therefore there is an urgent need to develop biotechnological processes for their production and extraction from plant raw materials and microorganisms.

Abstract Background Erythritol, a natural polyol, is a low-calorie sweetener synthesized by a number of microorganisms, such as Moniliella pollinis. Yet, a widespread use of erythritol is limited by high production costs due to the need for cultivation on glucose-rich substrates. This study explores the potential of using Trichoderma reesei as an alternative host for erythritol production, as this saprotrophic fungus can be cultivated on lignocellulosic biomass residues. The objective of this study was to evaluate whether such an alternative host would lead to a more sustainable and economically viable production of erythritol by identifying suitable carbon sources for erythritol biosynthesis, the main parameters influencing erythritol biosynthesis and evaluating the feasibility of scaling up the defined process. Results Our investigation revealed that T. reesei can synthesize erythritol from glucose but not from other carbon sources like xylose and lactose. T. reesei is able to consume erythritol, but it does not in the presence of glucose. Among nitrogen sources, urea and yeast extract were more effective than ammonium and nitrate. A significant impact on erythritol synthesis was observed with variations in pH and temperature. Despite successful shake flask experiments, the transition to bioreactors faced challenges, indicating a need for further scale-up optimization. Conclusions While T. reesei shows potential for erythritol production, reaching a maximum concentration of 1 g/L over an extended period, its productivity could be improved by optimizing the parameters that affect erythritol production. In any case, this research contributes valuable insights into the polyol metabolism of T. reesei, offering potential implications for future research on glycerol or mannitol production. Moreover, it suggests a potential metabolic association between erythritol production and glycolysis over the pentose phosphate pathway.

As the global production of polymers exceeded 400 million tons in 2022, it is imperative that recycling rates are increased to prevent the predominant end-of-life handling through landfilling and incineration processes. With an increasing reliance on polyurethane (PU), the 2022 global production of PU reached almost 26 million tons. As PU is mainly utilised as a thermoset material, the extensive cross-linked networks render melting and remolding processes known from thermoplastic materials incompatible. As such, the majority of PU that is recycled is processed through mechanical shredding and gluing processes or chemical recycling via glycolysis and acidolysis processes for polyol recovery, all providing a secondary material with properties different from the parent material. Here, we show that the well-established acidolysis process can be used to both depolymerise PU and separate the polyol and dianiline adducts with a specific focus on analysing and valorising the dianiline component arising from the hard segment of PU. By evaluation of the reaction outcome from acidolysis of flexible PU foam with succinic acid, adipic acid or phthalic acid under neat conditions, succinic acid was found to form the corresponding succinimide of toluene diamines that is readily separable from the polyol. The toluene diamine could in turn be reformed through ruthenium-catalysed hydrogenation or simple hydrolysis. Ultimately, the combined acidolysis/hydrolysis of a flexible PU foam yields the polyol and dianiline in a combined 83 wt% recovery. A similar recovery rate was achieved for a commercial rebonded flexible foam. As current PU recycling methods only target the polyol fraction often obtained in a low quality, this advancement shows that current industrially applied acidolysis could be altered so that both the diamines and polyol can be obtained from flexible PU foam. Preliminary results show that the process is applicable to rigid PU foams, a PU fraction that is difficult to recycle due to its molecular complexity. Finally, a mechanistic pathway is suggested to account for the observed product distributions. [ABSTRACT FROM AUTHOR]

A bio-based flame retardant nickel phytate (PA-Ni) was synthesized and combined with soybean oil-based polyol (SO) to create a green rigid polyurethane foam (RPUF) with enhanced compressive strength, good thermal stability and flame retardant. The results showed that the RPUF-SO2/Ni3 with 3 wt% PA-Ni had the highest initial and termination temperature, maximum thermal decomposition rate temperature and carbon residue, and better thermal stability. Its limiting oxygen index was increased by 2.6% compared with RPUF-SO2 without PA-Ni added, and the peak heat release rate (PHRR) and total heat release rate (THR) were reduced by 14.92% and 19.92%, respectively. In addition, RPUF-SO2/Ni3 had the lowest Ds under the conditions of flame (18.90) and flameless (22.41), and had the best smoke suppression effect. And the compressive strength of RPUF-SO/Ni3 was significantly enhanced by the addition of PA-Ni. The results show that the improvement of flame retardancy of RPUF is mainly the result of the combined effect of gas-phase and condensed-phase flame retardancy, among which the flame retardancy of RPUF-SO/Ni3 was the best. The current findings offer a practical way to produce green and low-carbon RPUF as well as promising prospects for the material's safe application. [ABSTRACT FROM AUTHOR]

The study of diffusion in biological materials is crucial for fields like food science, engineering, and pharmaceuticals. Research that combines numerical and analytical methods is needed to better understand diffusive phenomena across various dimensions and under variable boundary conditions within food matrices. This study aims to bridge this gap by examining the diffusion of substances through biological materials analytically and numerically, calculating diffusivity and conducting surface analysis. The research proposes a process for sweetening Bing-type cherries (Prunus avium) using sucrose/xylitol solutions and a staining technique utilising erythrosine and red gardenia at varying concentrations (119, 238 and 357 ppm) and temperatures (40, 50 and 60 °C). Given the fruit's epidermis resistance, the effective diffusivities of skin were inferior to those in flesh. Temperature and concentration synergise in enhancing diffusion coefficients and dye penetration within the food matrix (357 ppm and 60 °C). Red gardenia displayed significant temperature-dependent variation (p = 0.001), whereas erythrosine dye remained stable by temperature changes (p > 0.05). Gardenia's effective diffusivities in cherry flesh and skin, at 357 ppm and 60 °C, 3.89E−08 and 6.61E−09 m2/s, respectively, significantly differed from those obtained at lower temperatures and concentrations. The results highlight the temperature-concentration impacts on mass transfer calculations for food colouring processes and preservation methodologies. [ABSTRACT FROM AUTHOR]

Polyurethane foam compositions derived from bioderived polyester polyols with various additives were evaluated for disintegration under composting conditions using the ISO 20200 standard and were characterized by thermogravimetric analysis, microscopy, infrared spectroscopy, and imaging to provide additional insight. Compared to polyether polyol-based polyurethanes, the bioderived polyurethanes were found to display increased disintegration with an average mass loss of 25.4 ± 3.6 weight percent when subjected to composting conditions for 45 days, suggesting that these materials are less likely to persist in the environment when compared to other types of commodity plastics. Additives such as carbon black and lignin added within the foam composition did not accelerate the disintegration. [ABSTRACT FROM AUTHOR]

Fusarium oxysporum f. sp. lentis (Fol) is considered the most destructive disease for lentil (Lens culinaris Medik.) worldwide. Despite the extensive studies elucidating plants' metabolic response to fungal agents, there is a knowledge gap in the biochemical mechanisms governing Fol-resistance in lentil. Τhis study aimed at comparatively evaluating the metabolic response of two lentil genotypes, with contrasting phenotypes for Fol-resistance, to Fol-inoculation. Apart from gaining insights into the metabolic reprogramming in response to Fol-inoculation, the study focused on discovering novel biomarkers to improve early selection for Fol-resistance. GC-MS-mediated metabolic profiling of leaves and roots was employed to monitor changes across genotypes and treatments as well as their interaction. In total, the analysis yielded 178 quantifiable compounds, of which the vast majority belonged to the groups of carbohydrates, amino acids, polyols and organic acids. Despite the magnitude of metabolic fluctuations in response to Fol-inoculation in both genotypes under study, significant alterations were noted in the content of 18 compounds, of which 10 and 8 compounds referred to roots and shoots, respectively. Overall data underline the crucial contribution of palatinitol and L-proline in the metabolic response of roots and shoots, respectively, thus offering possibilities for their exploitation as metabolic biomarkers for Fol-resistance in lentil. To the best of our knowledge, this is the first metabolomics-based approach to unraveling the effects of Fol-inoculation on lentil's metabolome, thus providing crucial information related to key aspects of lentil–Fol interaction. Future investigations in metabolic aspects of lentil–Fol interactions will undoubtedly revolutionize the search for metabolites underlying Fol-resistance, thus paving the way towards upgrading breeding efforts to combat fusarium wilt in lentil. [ABSTRACT FROM AUTHOR]

Recyclability of polyurethane materials is significant to relieve environmental problems caused by damaged polymers. Inspired by plenty of self‐healing properties based on dynamic covalent bonds. A high mechanical strength and thermally reversible polyurethane adhesive are acquired through co‐polymerization of poly‐1,4‐butylene adipate glycol (PBA), soybean oil‐based polyol (MESO), and toluene diisocyanate (TDI) whose linear polymer chains are constructed by Diels–Alder reaction between furfuryl alcohol (FA) and bismaleimide (BMI), named DAPU. Further, the obtained polyurethane adhesives show great recyclability, mechanical performance (Whose tensile strength can reach 91.7 MPa), and appropriate self‐healing ability through the thermally reversible Diels–Alder covalent bonds and hydrogen bonds between urethane groups, which may pave a way for further development of recyclable materials. [ABSTRACT FROM AUTHOR]

Sulfate radical–based advanced oxidation processes (SR-AOPs) are renowned for their exceptional capacity to degrade refractory organic pollutants due to their wide applicability, cost-effectiveness, and swift mineralization and oxidation rates. The primary sources of radicals in AOPs are persulfate (PS) and peroxymonosulfate (PMS) ions, sparking significant interest in their mechanistic and catalytic aspects. To develop a novel nanocatalyst for SR-AOPs, particularly for PMS activation, we synthesized carbon-coated FeCo nanoparticles (NPs) using solvothermal methods based on the polyol approach. Various synthesis conditions were investigated, and the NPs were thoroughly characterized regarding their structure, morphology, magnetic properties, and catalytic efficiency. The FeCo phase was primarily obtained at [OH−] / [Metal] = 26 and [Fe] / [Co] = 2 ratios. Moreover, as the [Fe]/[Co] ratio increased, the degree of xylose carbonization to form a carbon coating (hydrochar) on the NPs also increased. The NPs exhibited a spherical morphology with agglomerates of varying sizes. Vibrating-sample magnetometer analysis (VSM) indicated that a higher proportion of iron resulted in NPs with higher saturation magnetization (up to 167.8 emu g−1), attributed to a larger proportion of FeCo bcc phase in the nanocomposite. The best catalytic conditions for degrading 100 ppm Rhodamine B (RhB) included 0.05 g L−1 of NPs, 2 mM PMS, pH 7.0, and a 20-min reaction at 25 °C. Notably, singlet oxygen was the predominant specie formed in the experiments in the SR-AOP, followed by sulfate and hydroxyl radicals. The catalyst could be reused for up to five cycles, retaining over 98% RhB degradation, albeit with increased metal leaching. Even in the first use, dissolved Fe and Co concentrations were 0.8 ± 0.3 and 4.0 ± 0.5 mg L−1, respectively. The FeCo catalyst proved to be effective in dye degradation and offers the potential for further refinement to minimize Co2+ leaching. [ABSTRACT FROM AUTHOR]