22 research outputs found

    Technological Advances in Winery Wastewater Treatment: A Comprehensive Review

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    The commercial production of wine is directly linked to the use of large amounts of fresh water coupledwith the generation of copious amounts of wastewater containing significant amounts of organic andinorganic substances. The impact of this waste stream on the environment has required the wine industryto implement certain protocols in wastewater management to comply with respective effluent dischargeregulations as set out by local authorities. Reduced accessibility to good quality water resources in recentyears has forced wineries to consider more efficient wastewater management strategies to improve waterrecovery and re-use, thereby promoting more sustainable wine production and minimizing the impact onstressed water resources. This review presents a comprehensive overview of established and emerging,physicochemical, biological, advanced oxidation and hybrid wastewater treatment technologies specificallyapplicable to the wine producing industry. Herein, winery wastewater composition and treatmenttechniques, environmental implications, knowledge gaps, technological operational challenges, alternativedisposal and recycling options of treated winery wastewater are critically evaluated

    Membrane supports designed for Pd membranes

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    Unique properties such as high permeance and a theoretically infinite selectivity to hydrogen gas exhibited by Palladium (Pd)-based membranes have caused thin Palladium films to emerge as an attractive method to separate and purify hydrogen from syngas. Pd-based membrane costs are a considerable economic hindrance to transforming this technology into a commonly applied gas separation technology, hence, the cost of these membranes needs to be reduced significantly. Cost reduction can be achieved by utilising composite membranes, composed of a thin dense layer of a Pd alloy deposited onto a porous support structure. While significant research has focused on Pd-based top layer optimisation, the physical properties of each sublayer have all but been ignored. In order to address challenges such as stability and durability of membranes, membrane production and operation costs more effectively, the current work aims to look at each layer as an integral part of the membrane system instead of unlinked individual layers. The end product of Pd-based membrane development should exhibit the following characteristics; a) defect-free continuous films, without protruding defects which would negatively affect the quality of the collected permeate gas, b) mechanically and chemically stable films, to hinder the formation of defects during the lifetime of the membrane under operating conditions, c) the film should have minimum thickness required in order to obtain a) and b) as excessive thickness will have a detrimental impact on H2 permeance and material cost. Please click Additional Files below to see the full abstract

    Synthesis, characterisation and evaluation of IrO2 based binary metal oxide electrocatalysts for oxygen evolution reaction

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    IrO2, IrxRu1-xO2, IrxSnx-1O2 and IrxTax-1O2 (1 ≥ x ≥ 0.7) were synthesized, characterised and evaluated as electrocatalysts for the oxygen evolution reaction in solid polymer electrolyte electrolysers. The electrocatalysts were synthesised by adapting the Adams fusion method. The physical properties of the electrocatalysts were characterised by scanning electron microscopy, transmission electron microscopy and x-ray diffraction. Electrochemical activity of the electrocatalysts toward the oxygen evolution reaction was evaluated by cyclic voltammetry and chronoamperometry. X-ray diffraction revealed no phase separation when RuO2 or SnO2 was introduced into the IrO2 lattice suggesting that solid solutions were formed. Transmission electron microscope analysis revealed nanosize particles for all synthesised metal oxides. Crystallinity increased with the addition of RuO2 and SnO2 while a suppression of crystal growth was observed with the addition of Ta2O5 to IrO2. Chronoamperometry revealed that the addition of all the secondary metal oxides to IrO2 resulted in improved catalytic performance. Ir0.7Ru0.3O2 was identified as the most promising electrocatalyst for the oxygen evolution reaction. Keywords:Web of Scienc

    A review of the processes associated with the removal of oil in water pollution

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    Water plays an essential role in production and refining processes. Many industries that use petrochemicals also require water, especially for cleaning purposes. The wastewaters released by these processes are often rich in petroleum pollutants, which requires significant treatment prior to disposal. The presence of petroleum contaminants in rivers and oceans is a significant threat to human health, as well as to many animal species. A current challenge for most industries and conventional effluent treatment plants is compliance with accepted disposal standards for oil-polluted wastewater. Of particular importance is the processing of dispersed oil in water, as well as oil in water emulsion. Conventional oil and water separation methods for processing oil in water contamination have several technology gaps in terms of applicability and efficiency. The removal and effective processing of dispersed oil and emulsions from oily wastewater is a costly and significant problem. The objective of this paper is to provide a review of the principles associated with oil in water emulsion separation, with the aim of providing a more definitive understanding of the terminology, processes, and methodologies, which will assist the development of a more efficient, innovative and environmentally friendly process for the separation of oily wastewater

    Development of FeCux/FeS/Graphite composite electrode materials for iron-based Alkaline batteries

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    In an attempt to enhance the electrochemical performance of the iron-based electrode, an iron-core copper-shell nano-structured material was synthesized and incorporated with ferrous sulphide, and graphite additives. An electrically conductive nickel mesh as a current collector, coupled with a low-cost hot-pressing technique, was employed to formulate the electrodes. The ferrous and graphite integrated iron-core copper-shell nano-structured negative electrode was investigated for applications in Fe-based alkaline batteries energy storage. FeCu0.25/15%FeS/5%C composite electrode delivered a specific discharge capacity of 385 mAh g-1 an approximately 71% coulombic efficiency. The nominal specific capacity of the electrode exhibited negligible capacity degradation after 40 cycles. Ex-situ X-ray Diffraction characterisations and scanning electrode microscopy images of both the fresh and the discharged electrode surfaces show that particle arrangement was still intact after 40 cycles, with negligible particle agglomeration compared to the pure iron electrode surface which was marked with massive agglomeration

    Optimization of gas diffusion electrode for polybenzimidazole-based high temperature proton exchange membrane fuel cell: Evaluation of polymer binders in catalyst layer

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    Gas diffusion electrodes (GDEs) prepared with various polymer binders in their catalyst layers (CLs) were investigated to optimize the performance of phosphoric acid doped polybenzimidazole (PBI)-based high temperature proton exchange membrane fuel cells (HT-PEMFCs). The properties of these binders in the CLs were evaluated by structure characterization, electrochemical analysis, single cell polarization and durability test. The results showed that polytetrafluoroethylene (PTFE) and polyvinylidene difluoride (PVDF) are more attractive as CL binders than conventional PBI or Nafion binder. At ambient pressure and 160 o C, the maximum power density can reach w 0.61 W cm-2 (PTFE GDE), and the current density at 0.6 V is up to ca. 0.52 A cm-2 (PVDF GDE), with H2/air and a platinum loading of 0.5 mg cm-2 on these electrodes. Also, both GDEs showed good stability for fuel cell operation in a short term durability test.Web of Scienc

    Ex-situ electrochemical characterization of iro2 synthesized by a modified Adams fusion method for the oxygen evolution reaction

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    The development of highly stable and active electrocatalysts for the oxygen evolution reaction (OER) has attracted significant research interest. IrO2 is known to show good stability during the OER however it is not known to be the most active. Thus, significant research has been dedicated to enhance the activity of IrO2 toward the OER. In this study, IrO2 catalysts were synthesized using a modified Adams fusion method. The Adams fusion method is simple and is shown to directly produce nano-sized metal oxides. The effect of the Ir precursor salt to the NaNO3 ratio and the fusion temperature on the OER activity of the synthesized IrO2 electrocatalysts, was investigated. The OER activity and durability of the IrO2 electrocatalysts were evaluated ex-situ via cyclic voltammetry (CV), chronopotentiometry (CP), electrochemical impedance spectroscopy (EIS) and linear sweep voltammetry (LSV)

    Membrane electrode assemblies with low noble metal loadings for hydrogen production from solid polymer electrolyte water electrolysis

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    High performance membrane electrode assemblies (MEAs) with low noble metal loadings (NMLs) were developed for solid polymer electrolyte (SPE) water electrolysis. The electro- chemical and physical characterization of the MEAs was performed by IeV curves, elec- trochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM). Even though the total NML was lowered to 0.38 mg cm-2, it still reached a high performance of 1.633 V at 2 A cm-2 and 80 o C, with IrO2 as anode catalyst. The influences of the ionomer content in the anode catalyst layer (CL) and the cell temperature were investigated with the purpose of optimizing the performance. SEM and EIS measurements revealed that the MEA with low NML has very thin porous cathode and anode CLs that get intimate contact with the electrolyte membrane, which makes a reduced mass transport limitation and lower ohmic resistance of the MEA. A short-term water electrolysis operation at 1 A cm-2 showed that the MEA has good stability: the cell voltage maintained at ~1.60 V without distinct degradation after 122 h operation at 80 o C and atmospheric pressure.Web of Scienc

    Membrane electrode assemblies with low noble metal loadings for hydrogen production from solid polymer electrolyte water electrolysis

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    High performance membrane electrode assemblies (MEAs) with low noble metal loadings (NMLs) were developed for solid polymer electrolyte (SPE) water electrolysis. The electro- chemical and physical characterization of the MEAs was performed by IeV curves, elec- trochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM). Even though the total NML was lowered to 0.38 mg cm-2, it still reached a high performance of 1.633 V at 2 A cm-2 and 80 o C, with IrO2 as anode catalyst. The influences of the ionomer content in the anode catalyst layer (CL) and the cell temperature were investigated with the purpose of optimizing the performance. SEM and EIS measurements revealed that the MEA with low NML has very thin porous cathode and anode CLs that get intimate contact with the electrolyte membrane, which makes a reduced mass transport limitation and lower ohmic resistance of the MEA. A short-term water electrolysis operation at 1 A cm-2 showed that the MEA has good stability: the cell voltage maintained at ~1.60 V without distinct degradation after 122 h operation at 80 o C and atmospheric pressure.Web of Scienc
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