I urval från Stockholms universitets publikationsdatabas

• Lignin-first biorefining of Nordic poplar to produce cellulose fibers could displace cotton production on agricultural lands

  2022. Anneli Adler (et al.). Joule 6 (8), 1845-1858

  Artikel

  Here, we show that lignin-first biorefining of poplar can enable the production of dissolving cellulose pulp that can produce regenerated cellulose, which could substitute cotton. These results in turn indicate that agricultural land dedicated to cotton could be reclaimed for food production by extending poplar plantations to produce textile fibers. Based on climate-adapted poplar clones capable of growth on marginal lands in the Nordic region, we estimate an environmentally sustainable annual biomass production of ∼11 tonnes/ha. At scale, lignin-first biorefining of this poplar could annually generate 2.4 tonnes/ha of dissolving pulp for textiles and 1.1 m³ biofuels. Life cycle assessment indicates that, relative to cotton production, this approach could substantially reduce water consumption and identifies certain areas for further improvement. Overall, this work highlights a new value chain to reduce the environmental footprint of textiles, chemicals, and biofuels while enabling land reclamation and water savings from cotton back to food production.

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• Microwave heating for sustainable valorization of almond hull towards high-added-value chemicals

  2022. Manuel Salgado-Ramos (et al.). Industrial crops and products (Print) 189

  Artikel

  Microwave (MW) treatment promotes homogeneous heating compared to conventional methods, thus increasing the recovery of high-added-value compounds and leading to a considerably lower amount of both by-products and side reactions. Therefore, the main goal of this work is to valorize almond hull (AH) via microwave (MW)-assisted radiation (0–200 W, 0–300 psi, 100–190 °C, 10–40 min). In this context, two different pathways were evaluated. Firstly, the transformation of AH into levulinic acid (LA), one of the major bio-based chemicals obtained from lignocellulosic biomass. The so-called almond hull extractives-free biomass (AH-EFB) led to the best results after using both Lewis (AlCl₃⋅6 H₂O, 1 mol/L, 87 % molar yield) and Brønsted (p-toluenesulfonic (p-TsOH), 0.25 mol/L, 91 % molar yield) acids, at 190 °C for 20 min. This latter not only provides a sustainable system in contrast to mineral acids such as H₂SO₄ or HCl, but also the possibility of being recovered and recycled for further transformations. In a parallel secondary experiment, the recovery of biologically active compounds (BACs) was studied separately. For this purpose, antioxidant assays and phenolic profiling were carried out, which demonstrated that MW was more efficient than traditional methods (i.e. soaking) based on obtained values in terms of scavenging activity and polyphenols. Overall, this valorization approach involves most of the Green Chemistry principles, thus contributing to the development of almond biorefineries.

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• Lignin-Chitosan Gel Polymer Electrolytes for Stable Zn Electrodeposition

  2023. Naroa Almenara Perez (et al.). ACS Sustainable Chemistry and Engineering

  Artikel

  Electrochemical energy storage technologies offer means to transition toward a decarbonized society and carbon neutrality by 2050. Compared to conventional lithium-ion batteries, aqueous zinc-ion chemistries do not require scarce materials or toxic and flammable organic-based electrolytes to function, making them favorable contenders in the scenario of intensifying climate change and supply chain crisis. However, environmentally benign and bio-based materials are needed to substitute fossil-based battery materials. Accordingly, this work taps into the possibilities of lignin together with chitosan to form gel polymer electrolytes (GPEs) for zinc-ion chemistries. A simple fabrication process enabling free-standing sodium lignosulfonate–chitosan and micellar lignosulfonate–kraft lignin–chitosan GPEs with diameters exceeding 80 mm is developed. The GPEs combine tensile strength with ductility, reaching Young’s moduli of 55 ± 4 to 940 ± 63 MPa and elongations at break of 14.1 ± 0.2 to 43.9 ± 21.1%. Competitive ionic conductivities ranging from 3.8 to 18.6 mS cm^–1 and electrochemical stability windows of up to +2.2 V vs Zn²⁺/Zn were observed. Given the improved interfacial adhesion of the GPEs with metallic Zn promoted by the anionic groups of the lignosulfonate, a stable cycling of the Zn anode is obtained. As a result, GPEs can operate at 5000 μA cm^–2 with no short-circuit and Coulombic efficiencies above 99.7%, outperforming conventional separator–liquid electrolyte configurations such as the glass microfiber separator soaked into 2 M ZnSO₄ aqueous electrolyte, which short-circuits after 100 μA cm^–2. This work demonstrates the potential of underutilized biorefinery side-streams and marine waste as electrolytes in the battery field, opening new alternatives in the sustainable energy storage landscape beyond LIBs.

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• A preliminary multistep combination of pulsed electric fields and supercritical fluid extraction to recover bioactive glycosylated and lipidic compounds from exhausted grape marc

  2023. Manuel Salgado-Ramos (et al.). Lebensmittel-Wissenschaft + Technologie 180

  Artikel

  This article reports the first multistep combination of pulsed electric field (PEF; 3 kV/cm, 100 kJ/kg, 2 Hz, 100 ms) and supercritical fluid extraction (SFE) with CO₂ (10–20 MPa, 25 mL/min [10% EtOH], 50 °C, 60 min) for exhausted grape marc (EGM). This current protocol was mainly created to recover bioactive glycosylated and lipidic compounds. In this regard, total antioxidant capacity (TAC) was enhanced up to 68% after PEF treatment compared to conventional soaking. However, re-extracting PEF-treated EGM after the application of SFE (PEF + SFE) boosted the efficiency by up to 87%. Several polyphenols (kaempferol, luteolin, scutellarin, and resveratrol, among others), together with other glycosylated structures, were identified by liquid chromatography coupled with mass spectrometry analysis. The bioactive lipidic compounds extracted by SFE, along with the carbohydrate fraction (free sugars) favourably extracted by PEF pre-treatment (mainly glucose, but also fructose and sucrose), were concurrently detected by nuclear magnetic resonance. The remaining solid fraction after treatment was also characterised. Different microscopic morphology was observed by scanning electron microscopy (SEM) on untreated, PEF, and PEF + SC–CO₂–treated EGM. Differential thermogravimetric (DTG) curves determined by thermogravimetric analysis (TGA) also suggested alternative and potential means for the valorisation of this matrix.

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• Mechanically recyclable melt-spun fibers from lignin esters and iron oxide nanoparticles: towards circular lignin materials

  2023. Unnimaya Thalakkale Veettil (et al.). Green Chemistry

  Artikel

  The inferior thermoplastic properties have limited production of melt-spun fibers from lignin. Here we report on the controlled esterification of softwood kraft lignin (SKL) to enable scalable, solvent-free melt spinning of microfibers using a cotton candy machine. We found that it is crucial to control the esterification process as melt-spun fibers could be produced from lignin oleate and lignin stearate precursors with degrees of esterification (DE) ranging from 20-50%, but not outside this range. To fabricate a functional hybrid material, we incorporated magnetite nanoparticles (MNPs) into the lignin oleate fibers by melt blending and subsequent melt spinning. Thermogravimetric analysis and X-ray diffraction studies revealed that increasing the weight fraction of MNPs led to improved thermal stability of the fibers. Finally, we demonstrated adsorption of organic dyes, magnetic recovery, and recycling via melt spinning of the regular and magnetic fibers with 95% and 83% retention of the respective adsorption capacities over three adsorption cycles. The mechanical recyclability of the microfibers represents a new paradigm in lignin-based circular materials.

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