Search Results (14)

Spent coffee grounds (SCG) are a widely available agro-industrial residue rich in carbon and phenolic compounds, presenting significant potential for biotechnological valorization. This study evaluated the use of SCG as a suitable substrate for fungal laccase production and the application of the resulting fermented biomass (RFB), a mixture of fermented SCG and fungal biomass as a biosorbent for textile dye removal. Two fungal strains, namely Lentinus crinitus UCP 1206 and Trametes sp. UCP 1244, were evaluated in both submerged (SmF) and solid-state fermentation (SSF) using SCG. L. crinitus showed superior performance in SSF, reaching 14.62 U/g of laccase activity. Factorial design revealed that a lower SCG amount (5 g) and higher moisture (80%) and temperature (30 °C ± 0.2) favored enzyme production. Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) analyses confirmed significant structural degradation of SCG after fermentation, especially in SSF. Furthermore, SCG and RFB were chemically activated and evaluated as biosorbents. The activated carbon from SCG (ACSCG) and RFB (ACRFB) exhibited high removal efficiencies for Remazol dyes, comparable to commercial activated carbon. These findings highlight the potential of SCG as a low-cost, sustainable resource for enzyme production and wastewater treatment, contributing to circular bioeconomy strategies. Full article

Redox flow batteries (RFB) often operate at extreme pH conditions and may require cooling to prevent high temperatures. The stability of the battery membranes at these extreme pH-values at high temperatures is still largely unknown. In this paper, a systematic screening of the performance and stability of nine commercial membranes at pH 14 and pH ≤ 0 with temperatures up to 80 °C is conducted in an organic aqueous RFB. Swelling, area resistance, diffusion crossover, battery performance and membrane stability after 40–80 °C temperature treatment are shown, after which a recommendation is made for different user scenarios. The Aquivion E98-05 membrane performed best for both the Tiron/2,7-AQDS battery and the DHPS/Fe(CN)₆ battery at 40 mA/cm², with stable results after 1 week of storage at 80 °C. At 80 mA/cm², E-620-PE performed best in the DHPS/Fe(CN)₆ battery, while Sx-050DK performed best in the Tiron/2,7-AQDS battery. Full article

Loop-mediated isothermal amplification, LAMP, is nowadays the most popular isothermal nucleic acid amplification technique, and as such, several commercial, ready-to-use master mixes have flourished. Unfortunately, independent studies to determine their performance are limited. The current study performed an independent evaluation of the existing ready-to-use commercial LAMP master mixes WarmStart^® LAMP Kit, LavaLAMP™ DNA Master Mix, Saphir Bst Turbo GreenMaster, OptiGene Fast Master Mix ISO-004, and SynLAMP Mix. To reduce bias, three different genes, namely ttr (Salmonella spp.), rfbE (E. coli O157), and hly (Listeria monocytogenes), were targeted. The comparison was based on amplification speed, performance with decreasing DNA concentrations, and the effect of five typical LAMP reaction additives (betaine, DMSO, pullulan, TMAC, and GuHCl). Significant differences were observed among the different master mixes. OptiGene provided the fastest amplification and showed less detrimental effects associated with the supplements evaluated. Out of the chemicals tested, pullulan provided the best results in terms of amplification speed. It is noteworthy that the different additives impacted the master mixes differently. Overall, the current study provides insights into the performance of commercial LAMP master mixes, which can be of value for the scientific community to better select appropriate reagents when developing new methods. Full article

This research tested whether mycorrhizae can rejuvenate the water quality and pollinator functions of degraded riparian forested buffers (RFBs) in agricultural landscapes while facilitating indigenous Abenaki access to ancestral lands. Two plots within a degraded RFB were restored with a multi-functional plant community, one plot inoculated with commercial mycorrhizae and the other without. A control plot remained in a degraded state dominated by the invasive shrub Rhamnus cathartica. The restoration palette of 32 plants included 28 species useful to the Abenaki, representing opportunities for phosphorus removal through harvesting. Monitoring data from 2020 to 2023 indicated consistently greater plant diversity in the restored plots, with 58 newcomers appearing. Although the total phosphorus (P) decreased over time in all the treatments, the greatest decrease was in the uninoculated plot, likely due to pathogenicity from the commercial inoculant or the spatial variability of soil and light. The biomass P of five plant species differed among the species but not among the treatment plots. Nonetheless, Abenaki harvesting removed P and can be an effective form of phytoremediation, phytoextraction. However, this research revealed trade-offs between P mitigation, indigenous use, and pollinator functions of the RFB. Fostering higher biodiversity, Indigenous land access, and P mitigation are important solution-oriented aims to balance when restoring degraded RFBs. Full article

Non-aqueous redox flow batteries (NARFBs) have been attracting much attention because they can significantly increase power and energy density compared to conventional RFBs. In this study, novel pore-filled anion-exchange membranes (PFAEMs) for application to a NAPFB employing metal polypyridyl complexes (i.e., Fe(bpy)₃²⁺/Fe(bpy)₃³⁺ and Co(bpy)₃²⁺/Co(bpy)₃³⁺) as the redox species are successfully developed. A porous polyethylene support with excellent solvent resistance and mechanical strength is used for membrane fabrication. The PFAEMs are prepared by filling an ionic liquid monomer containing an imidazolium group and a crosslinking agent into the pores of the support film and then performing in situ photopolymerization. As a result, the prepared membranes exhibit excellent mechanical strength and stability in a non-aqueous medium as well as high ion conductivity. In addition, a low crossover rate for redox ion species is observed for the prepared membranes because they have relatively low swelling characteristics in non-aqueous electrolyte solutions and low affinity for the metal-complex redox species compared to a commercial membrane. Consequently, the PFAEM is revealed to possess superior battery performance than a commercial membrane in the NARFB tests, showing high energy efficiency of about 85% and stable operation for 100 cycles. Full article

Redox flow batteries represent a captivating class of electrochemical energy systems that are gaining prominence in large-scale storage applications. These batteries offer remarkable scalability, flexible operation, extended cycling life, and moderate maintenance costs. The fundamental operation and structure of these batteries revolve around the flow of an electrolyte, which facilitates energy conversion and storage. Notably, the power and energy capacities can be independently designed, allowing for the conversion of chemical energy from input fuel into electricity at working electrodes, resembling the functioning of fuel cells. This work provides a comprehensive overview of the components, advantages, disadvantages, and challenges of redox flow batteries (RFBs). Moreover, it explores various diagnostic techniques employed in analyzing flow batteries. The discussion encompasses the utilization of RFBs for large-scale energy storage applications and summarizes the engineering design aspects related to these batteries. Additionally, this study delves into emerging technologies, applications, and challenges in the realm of redox flow batteries. Full article

Redox flow batteries (RFB) are considered one of the most promising electrochemical energy storage technologies for stationary storage applications, especially for long duration energy storage services. RFBs are electrochemical energy converters that use flowing media as or with active materials, where the electrochemical reactions can be reversed. Knowledge of technical standards and other regulations lay the foundations for successful and safe commercialization of products through uniform instructions and generally applicable rules. A small number of papers on safety and regulatory issues of RFBs are reported in the literature, mainly for two reasons. First, because this technology is considered safe; and second, because most of the publications have been limited to short-term characterization studies of materials in chemistry. This paper aims to help fill this gap, providing researchers and students with introductory knowledge on the safety and regulatory aspects of RFBs, mainly from an electrical and hydraulic point of view. The reader is referred to specific regulations for deeper studies and analyses. Full article

The effective scaling-up of redox flow batteries (RFBs) can be facilitated upon lowering the capital costs. The application of ubiquitous manganese along with hydrogen (known as H₂−Mn regenerative fuel cells (RFC)) is seen as an effective solution for this purpose. Here, we aim to evaluate different positive electrodes so as to improve the key performance metrics of the H₂/Mn RFC, namely electrolyte utilization, energy efficiency, and peak power densities. Commercially available carbon paper and graphite felt are used to show that the latter provides better key performance indicators (KPIs), which is consistent with the results reported for standard all-vanadium RFBs in the literature. Even better KPIs are obtained when an in-house carbon catalyst layer (CCL) is employed in combination with graphite felt electrodes (e.g., more than 80% energy efficiency, >0.5 W cm⁻² peak power density and electrolyte utilization of 20 Ah L⁻¹ for felt and carbon metal fabric (CMF), prepared by means of electrospinning and carbonization, in comparison with about 75% energy efficiency 0.45 W cm⁻² peak power density and 11 Ah L⁻¹ electrolyte utilization for felt on its own). It is envisaged that if the electrochemical performance of CCLs can be optimized then it could open up new opportunities for the commercial exploitation of H₂−Mn systems. Full article

The detection of both viable and viable but non-culturable (VBNC) Escherichia coli O157:H7 is a crucial part of food safety. Traditional culture-dependent methods are lengthy, expensive, laborious, and unable to detect VBNC. Hence, there is a need to develop a rapid, simple, and cost-effective detection method to differentiate between viable/dead E. coli O157:H7 and detect VBNC cells. In this work, recombinase polymerase amplification (RPA) was developed for the detection of viable E. coli O157:H7 through integration with propidium monoazide (PMAxx). Initially, two primer sets, targeting two different genes (rfbE and stx) were selected, and DNA amplification by RPA combined with PMAxx treatment and the lateral flow assay (LFA) was carried out. Subsequently, the rfbE gene target was found to be more effective in inhibiting the amplification from dead cells and detecting only viable E. coli O157:H7. The assay’s detection limit was found to be 10² CFU/mL for VBNC E. coli O157:H7 when applied to spiked commercial beverages including milk, apple juice, and drinking water. pH values from 3 to 11 showed no significant effect on the efficacy of the assay. The PMAxx-RPA-LFA was completed at 39 °C within 40 min. This study introduces a rapid, robust, reliable, and reproducible method for detecting viable bacterial counts. In conclusion, the optimised assay has the potential to be used by the food and beverage industry in quality assurance related to E. coli O157:H7. Full article

Composite anion-exchange membranes (AEMs) consisting of a porous substrate and a vinyl imidazolium poly(phenylene oxide) (VIMPPO)/acrylamide copolymer layer were fabricated in a straightforward process, for use in redox flow batteries. The porous substrate was coated with a mixture of VIMPPO and acrylamide monomers, then subsequently exposed to UV irradiation, in order to obtain a radically cured ion-exchange coating. Combining VIMPPO with low-value reagents allowed to significantly reduce the amount of synthesized ionomer used to fabricate the mem- brane down to 15%. Varying the VIMPPO content also allowed tuning the ionic transport properties of the resulting AEM. A series of membranes with different VIMPPO/acrylamides ratios were prepared to assess the optimal composition by studying the changes of membranes properties—water uptake, area resistivity, permeability, and chemical stability. Characterization of the membranes was followed by cycling experiments in a vanadium RFB (VRFB) cell. Among three composite membranes, the one with VIMPPO 15% w/w—reached the highest energy efficiency (75.1%) matching the performance of commercial ion-exchange membranes (IEMs) used in VRFBs (Nafion^® N 115: 75.0% and Fumasep^® FAP 450: 73.0%). These results showed that the proposed composite AEM, fabricated in an industrially oriented process, could be considered to be a lower-cost alternative to the benchmarked IEMs. Full article

Despite intense research in the field of aqueous organic redox flow batteries, low molecular stability of electroactive compounds limits further commercialization. Additionally, currently used methods typically cannot differentiate between individual capacity fade mechanisms, such as degradation of electroactive compound and its cross-over through the membrane. We present a more complex method for in situ evaluation of (electro)chemical stability of electrolytes using a flow electrolyser and a double half-cell including permeation measurements of electrolyte cross-over through a membrane by a UV–VIS spectrometer. The method is employed to study (electro)chemical stability of acidic negolyte based on an anthraquinone sulfonation mixture containing mainly 2,6- and 2,7-anthraquinone disulfonic acid isomers, which can be directly used as an RFB negolyte. The effect of electrolyte state of charge (SoC), current load and operating temperature on electrolyte stability is tested. The results show enhanced capacity decay for fully charged electrolyte (0.9 and 2.45% per day at 20 °C and 40 °C, respectively) while very good stability is observed at 50% SoC and lower, even at 40 °C and under current load (0.02% per day). HPLC analysis conformed deep degradation of AQ derivatives connected with the loss of aromaticity. The developed method can be adopted for stability evaluation of electrolytes of various organic and inorganic RFB chemistries. Full article

Currently, energy storage technologies are becoming essential in the transition of replacing fossil fuels with more renewable electricity production means. Among storage technologies, redox flow batteries (RFBs) can represent a valid option due to their unique characteristic of decoupling energy storage from power output. To push RFBs further into the market, it is essential to include low-cost materials such as new generation membranes with low ohmic resistance, high transport selectivity, and long durability. This work proposes a composite membrane for vanadium RFBs and a method of preparation. The membrane was prepared starting from two polymers, meta-polybenzimidazole (6 μm) and porous polypropylene (30 μm), through a gluing approach by hot-pressing. In a vanadium RFB, the composite membrane exhibited a high energy efficiency (~84%) and discharge capacity (~90%) with a 99% capacity retention over 90 cycles at 120 mA·cm⁻², exceeding commercial Nafion^® NR212 (~82% efficiency, capacity drop from 90% to 40%) and Fumasep^® FAP-450 (~76% efficiency, capacity drop from 80 to 65%). Full article

Among various components commonly used in redox flow batteries (RFBs), the separator plays a significant role, influencing resistance to current as well as capacity decay via unintended crossover. It is well-established that the ohmic overpotential is dominated by the membrane and interfacial resistance in most aqueous RFBs. The ultimate goal of engineering membranes is to improve the ionic conductivity while keeping crossover at a minimum. One of the major issues yet to be addressed is the contribution of interfacial phenomena in the influence of ionic and water transport through the membrane. In this work, we have utilized a novel experimental system capable of measuring the ionic crossover in real-time to quantify the permeability of ionic species. Specifically, we have focused on quantifying the contributions from the interfacial resistance to ionic crossover. The trade-off between the mass and ionic transport impedance caused by the interface of the membranes has been addressed. The MacMullin number has been quantified for a series of electrolyte configurations and a correlation between the ionic conductivity of the contacting electrolyte and the Nafion^® membrane has been established. The performance of individual ion-exchange membranes along with a stack of various separators have been explored. We have found that utilizing a stack of membranes is significantly beneficial in reducing the electroactive species crossover in redox flow batteries compared to a single membrane of the same fold thickness. For example, we have demonstrated that the utilization of five layers of Nafion^® 211 membrane reduces the crossover by 37% while only increasing the area-specific resistance (ASR) by 15% compared to a single layer Nafion^® 115 membrane. Therefore, the influence of interfacial impedance in reducing the vanadium ion crossover is substantially higher compared to a corresponding increase in ASR, indicating that mass and ohmic interfacial resistances are dissimilar. We have expanded our analysis to a combination of commercially available ion-exchange membranes and provided a design chart for membrane selection based on the application of interest (short duration/high-performance vs. long-term durability). The results of this study provide a deeper insight into the optimization of all-vanadium redox flow batteries (VRFBs). Full article

Redox flow batteries (RFBs), provide a safe and cost-effective means of storing energy at grid-scale, and will play an important role in the decarbonization of global electricity networks. Several approaches have been explored to improve their efficiency and power density, and recently, cell geometry modification has shown promise in efforts to address mass transport limitations which affect electrochemical and overall system performance. Flow-by electrode configurations have demonstrated significant power density improvements in laboratory testing, however, flow-through designs with conductive felt remain the standard at commercial scale. Concentration gradients exist within these cells, limiting their performance. A new concept of redistributing reactants within the flow frame is introduced in this paper. This research shows a 60% improvement in minimum V³⁺ concentration within simulated vanadium redox flow battery (VRB/VRFB) cells through the application of static mixers. The enhanced reactant distribution showed a cell voltage improvement by reducing concentration overpotential, suggesting a pathway forward to increase limiting current density and cycle efficiencies in RFBs. Full article