We report the discovery of the hydrotropic properties of a recyclable aromatic acid, p-toluenesulfonic acid (p-TsOH), for potentially low-cost and efficient fractionation of wood through rapid and near-complete dissolution of lignin. Approximately 90% of poplar wood (NE222) lignin can be dissolved at 80°C in 20 min. Equivalent delignification using known hydrotropes, such as aromatic salts, can be achieved only at 150°C or higher for more than 10 hours or at 150°C for 2 hours with alkaline pulping. p-TsOH fractionated wood into two fractions: (i) a primarily cellulose-rich water-insoluble solid fraction that can be used for the production of high-value building blocks, such as dissolving pulp fibers, lignocellulosic nanomaterials, and/or sugars through subsequent enzymatic hydrolysis; and (ii) a spent acid liquor stream containing mainly dissolved lignin that can be easily precipitated as lignin nanoparticles by diluting the spent acid liquor to below the minimal hydrotrope concentration. Our nuclear magnetic resonance analyses of the dissolved lignin revealed that p-TsOH can depolymerize lignin via ether bond cleavage and can separate carbohydrate-free lignin from the wood. p-TsOH has a relatively low water solubility, which can facilitate efficient recovery using commercially proven crystallization technology by cooling the concentrated spent acid solution to ambient temperatures to achieve environmental sustainability through recycling of p-TsOH.

Scots pine planks were heat‐treated under steam in a temperature range of 100–240°C at every 20°C. Changes in chemical structure of the wood samples were examined with UV resonance Raman (UVRR) and Fourier transform infrared (FT‐IR) spectroscopies. Prior to the FT‐IR and UVRR analysis, the heartwood part of wood samples were ground and extracted with acetone. Both the extracts and the extracted samples were analyzed. In addition, Klason lignin contents of the samples were determined. The FT‐IR and UVRR spectroscopy were powerful techniques to monitor chemical changes in the heat‐treated wood samples. Results confirmed most of what determined previously by other research groups using different techniques. The UVRR and FT‐IR spectra of acetone extracts showed that lignin became partly acetone soluble after a heat treatment of 180°C or greater. Increased levels of free phenolic hydroxyl groups were detected in lignin, probably due to cleavages of β‐O‐aryl ether interunit linkages. The amount of extr...

In this study, we present willow wood as a new low-cost, renewable, and sustainable biomass source for the production of a highly porous activated carbon for application in energy storage devices. The obtained activated carbon showed favorable features required for excellent electrochemical performance such as high surface area (∼2 800 m² g^–1) and pore volume (1.45 cm³ g^–1), with coexistence of micropores and mesopores. This carbon material was tested as an electrode for supercapacitor application and showed a high specific capacitance of 394 F g^–1 at a current density of 1 A g^–1 and good cycling stability, retaining ∼94% capacitance after 5 000 cycles (at a current density of 5 A g^–1) in 6 M KOH electrolyte. The prepared carbon material also showed an excellent rate performance in a symmetrical two-electrode full cell configuration using 1 M Na₂SO₄ electrolyte, in a high working voltage of 1.8 V. The maximum energy density and power density of the fabricated symmetric cell reach 23 W h kg^–1 and 10 000 W kg^–1, respectively. These results demonstrate that willow wood can serve as a low-cost carbon feedstock for production of high-performance electrode material for supercapacitors.