Dual disintegration of microalgae biomass for cost-effective biomethane production: Energy and cost assessment.

The present study aims to enhance the biomethane production potential of microalgae via a dual disintegration process. During this process, the microalgae biomass was firstly subjected to cell wall weakening by thermochemical disintegration (TC) (50 to 80 °C), pH adjustment with alkali, NaOH (6 to 10) and time (0 to 10 min) and, secondly, by bacterial disintegration (BD). TC-BD disintegration was comparatively higher (33 %) than BD (24 %), TC (8.5 %), and control (7 %). A more significant VFA accumulation of 2816 mg/L was recorded for TC-BD. Similarly, a greater substrate anaerobic biodegradability was achieved in TC-BD (0.32 g COD /g COD) than BD (0.21 g COD /g COD), TC alone (0.09 gCOD/g COD) and control (0.08 g COD /g COD), respectively. The TC-BD achieves a positive net profit and an energy ratio of + 0.12 GJ/d and 1.03. The proposed dual disintegration has a promising future for commercialization.

MOF-Derived Cobalt@Mesoporous Carbon as Electrocatalysts for Oxygen Evolution Reaction: Impact of Organic Linker.

Water electrolysis has attracted scientists' attention as a green route for energy generation. However, the sluggish kinetics of oxygen evolution reaction (OER) remarkably increases the reaction overpotential. In this work, we developed Co-based nanomaterials as cost-effective, highly efficient catalysts for OER. In this regard, different Co-based metal-organic frameworks (MOFs) were synthesized using different organic linkers. After annealing under inert atmosphere, the corresponding Co-embedded mesoporous carbon (Co/MC) materials were produced. Among them, Co/MC synthesized using 2-methyl imidazole (Co/NMC-2MeIM) expressed the highest surface area (412 m2/g) compared to its counterparts. Furthermore, it expressed a higher degree of defects as depicted by Raman spectra. Co/NMC-2MeIM exhibited the best catalytic performance toward OER in alkaline medium. It afforded an overpotential of 292 mV at a current density of 10 mA cm-2 and a Tafel slope of 99.2 mV dec-1. The superior electrocatalytic performance of Co/NMC-2MeIM is attributed to its high content of Co3+ on the surface, high surface area, and enhanced electrical conductivity induced by nitrogen doping. Furthermore, its high content of pyridinic-N and high degree of defects remarkably enhance the charge transfer between the adsorbed oxygen species and the active sites. These results may pave the avenue toward further investigation of metal/carbon materials in a wide range of electrocatalytic applications.

Microwave-Assisted Solvothermal Synthesis of Mo-Doped TiO2 with Exceptional Textural Properties and Superior Adsorption Kinetics.

Assigned to their outstanding physicochemical properties, TiO2-based materials have been studied in various applications. Herein, TiO2 doped with different Mo contents (Mo-TiO2) was synthesized via a microwave-assisted solvothermal approach. This was achieved using titanium (IV) butoxide and molybdenum (III) chloride as a precursor and dodecylamine as a surface directing agent. The uniform effective heating delivered by microwave heating reduced the reaction time to less than 30 min, representing several orders of magnitude lower than conventional heating methods. The average particle size ranged between 9.7 and 27.5 nm and it decreased with increasing the Mo content. Furthermore, Mo-TiO2 revealed mesoporous architectures with a high surface area ranging between 170 and 260 m2 g-1, which is superior compared to previously reported Mo-doped TiO2. The performance of Mo-TiO2 was evaluated towards the adsorption of Rhodamine B (RhB). In contrast to TiO2, which revealed negligible adsorption for RhB, Mo-doped samples depicted rapid adsorption for RhB, with a rate that increased with the increase in Mo content. Additionally, Mo-TiO2 expressed enhanced adsorption kinetics for RhB compared to state-of-the-art adsorbents. The introduced synthesis procedure holds a grand promise for the versatile synthesis of metal-doped TiO2 nanostructures with outstanding physicochemical properties.

Solution combustion synthesis of Ni-based hybrid metal oxides for oxygen evolution reaction in alkaline medium.

Oxygen evolution reaction (OER) has arisen as an outstanding technology for energy generation, conversion, and storage. Herein, we investigated the synthesis of nickel-based hybrid metal oxides (Ni x M1-x O y ) and their catalytic performance towards OER. Ni x M1-x O y catalysts were synthesized by solution combustion synthesis (SCS) using the metal nitrates as oxidizer and glycine as fuel. Scanning electron microscope (SEM) micrographs display a porous morphology for the hybrid binary Ni x M1-x O y , the common feature of combusted materials. X-ray diffraction (XRD) of Ni x M1-x O y depicted well-defined diffraction peaks, which confirms the crystalline nature of synthesized catalysts. The particle size of as-synthesized materials ranges between 20 and 30 nm with a mesoporous nature as revealed by N2-physisorption. The electrocatalytic performance of the as-prepared materials was evaluated towards OER in alkaline medium. Among them, Ni x Co1-x O y showed the best catalytic performance. For instance, it exhibited the lowest overpotential at a current density of 10 mA cm-2 (404 mV), onset potential (1.605 V), and Tafel slope (52.7 mV dec-1). The enhanced electrocatalytic performance of Ni x Co1-x O y was attributed to the synergism between cobalt and nickel and the alteration of the electronic structure of nickel. Also, Ni x Co1-x O y afforded the highest Ni3+/Ni2+ when compared to other electrocatalysts. This leads to higher oxidation states of Ni species, which promote and improve the electrocatalytic activity.

Surfactant induced microwave disintegration for enhanced biohydrogen production from macroalgae biomass: Thermodynamics and energetics.

This research work aimed about the enhanced bio-hydrogen production from marine macro algal biomass (Ulva reticulate) through surfactant induced microwave disintegration (SIMD). Microwave disintegration (MD) was performed by varying the power from 90 to 630 W and time from 0 to 40 min. The maximum chemical oxygen demand (COD) solubilisation of 27.9% was achieved for MD at the optimal power (40%). A surfactant, ammonium dodecyl sulphate (ADS) is introduced in optimal power of MD which enhanced the solubilisation to 34.2% at 0.0035 g ADS/g TS dosage. The combined SIMD pretreatment significantly reduce the treatment time and increases the COD solubilisation when compared to MD. Maximum hydrogen yield of 54.9 mL H2 /g COD was observed for SIMD than other samples. In energy analysis, it was identified that SIMD was energy efficient process compared to others since SIMD achieved energy ratio of 1.04 which is higher than MD (0.38).

Electrochemical Performance of Na3V2(PO4)2F3 Electrode Material in a Symmetric Cell.

A NASICON-based Na3V2(PO4)2F3 (NVPF) cathode material is reported herein as a potential symmetric cell electrode material. The symmetric cell was active from 0 to 3.5 V and showed a capacity of 85 mAh/g at 0.1 C. With cycling, the NVPF symmetric cell showed a very long and stable cycle life, having a capacity retention of 61% after 1000 cycles at 1 C. The diffusion coefficient calculated from cyclic voltammetry (CV) and the galvanostatic intermittent titration technique (GITT) was found to be ~10-9-10-11, suggesting a smooth diffusion of Na+ in the NVPF symmetric cell. The electrochemical impedance spectroscopy (EIS) carried out during cycling showed increases in bulk resistance, solid electrolyte interphase (SEI) resistance, and charge transfer resistance with the number of cycles, explaining the origin of capacity fade in the NVPF symmetric cell. Finally, the postmortem analysis of the symmetric cell after 1000 cycles at a 1 C rate indicated that the intercalation/de-intercalation of sodium into/from the host structure occurred without any major structural destabilization in both the cathode and anode. However, there was slight distortion in the cathode structure observed, which resulted in capacity loss of the symmetric cell. The promising electrochemical performance of NVPF in the symmetric cell makes it attractive for developing long-life and cost-effective batteries.

Solution combustion synthesis of Ni/La2O3 for dry reforming of methane: tuning the basicity via alkali and alkaline earth metal oxide promoters.

The production of syngas via dry reforming of methane (DRM) has drawn tremendous research interest, ascribed to its remarkable economic and environmental impacts. Herein, we report the synthesis of K, Na, Cs, Li, and Mg-promoted Ni/La2O3 using solution combustion synthesis (SCS). The properties of the catalysts were determined by N2 physisorption experiments, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectrometry (XPS), and H2-TPR (temperature programmed reduction). In addition, their catalytic performance towards DRM was evaluated at 700 °C. The results demonstrated that all catalysts exhibited porous structures with high specific surface area, in particular, Mg-promoted Ni/La2O3 (Mg-Ni-La2O3) which depicted the highest surface area and highest pore volume (54.2 m2 g-1, 0.36 cm3 g-1). Furthermore, Mg-Ni-La2O3 exhibited outstanding catalytic performance in terms of activity and chemical stability compared to its counterparts. For instance, at a gas hourly space velocity (GHSV) of 30 000 mL g-1 h-1, it afforded 83.2% methane conversion and 90.8% CO2 conversion at 700 °C with no detectable carbon deposition over an operating period of 100 h. The superb DRM catalytic performance of Mg-Ni-La2O3 was attributed to the high specific surface area/porosity, strong metal-support interaction (MSI), and enhanced basicity, in particular the strong basic sites compared to other promoted catalysts. These factors remarkably enhance the catalytic performance and foster resistance to coke deposition.

A review on self-sustainable microbial electrolysis cells for electro-biohydrogen production via coupling with carbon-neutral renewable energy technologies.

Microbial electrolysis cell (MEC) technology is a promising bioelectrochemical hydrogen production technology that utilizes anodic bio-catalytic oxidation and cathodic reduction processes. MECs require a lower external energy input than water electrolysis; however, as they also require the application of external power sources, this inevitably renders MEC systems a less sustainable option. This issue is the main obstacle hindering the practical application of MECs. Therefore, this review aims to introduce a self-sustainable MEC technology by combining conventional MECs with advanced carbon-neutral technologies, such as solar-, microbial-, osmotic-, and thermoelectric-powers (and their combinations). Moreover, new approaches to overcome the thermodynamic barriers and attain self-sustaining MECs are discussed in detail, thereby providing a working principle, current challenges, and future perspective in the field. This review provides comprehensive insights into reliable hydrogen production as well as the latest trends towards self-sustainable MECs for practical application.

Natural clay-supported palladium catalysts for methane oxidation reaction: effect of alloying.

The catalytic combustion of methane (CCM) has been extensively studied owing to the wide use of methane in motor vehicles and power generation turbines. However, the absence of polarizability and the high C-H bond strength are considered to be the main drawbacks that limit its oxidation by traditional catalytic converters. Palladium-based catalysts are recognized as the benchmark catalysts for methane oxidation, especially under oxidizing conditions, and their activity is dependent on different parameters such as size, dispersion, and the nature of the support. Additionally, metal oxides are the most common supports used for CCM; however, they can become saturated with water, especially during steady-state operation at low temperatures, owing to their hydrophilic nature. This causes saturation of the active sites with OH species, which poisons the active centers of the catalyst, prevents activation of methane molecules, and induces catalyst sintering. Herein, we reported the synthesis of a binary palladium nanoalloy on a halloysite nanotube support (PdM@Hal). This one-pot synthesis procedure was performed via ultrasound-enhanced reduction of metal precursors in aqueous solution containing dispersed halloysite nanotubes, using NaBH4 as reducing agent. Transmission electron microscopy revealed that the synthesized PdM@Hal catalysts preserved the morphology of the pristine support after synthesis and calcination, with good dispersion of the catalyst on the surface of the support. Promoted metal-support interactions revealed enhanced catalytic performance, following the order PdNi > PdCo > Pd > PdCu, with activation energies of 68-94 kJ mol-1.

Enhanced photocatalytic performance of WON@porous TiO2 nanofibers towards sunlight-assisted degradation of organic contaminants.

In the last few decades, TiO2 has been widely used in different types of photocatalytic applications. However, the relatively large optical band gap (∼3.2 eV), low charge carrier mobility and consequently its low quantum efficiency limit its photocatalytic activity. Herein, we construct a novel nanostructured heterojunction of WON/TiO2 nanofibers (NFs) by integration of TiO2 nanofibers synthesized by electrospinning of a polymer solution containing a titanium(iv) butoxide precursor with WON nanoparticles fabricated via annealing of a WO3 precursor in dry ammonia at 700 °C. The synthesized photocatalysts were characterized using different spectroscopic techniques. Their photocatalytic performance towards the degradation of methyl orange, methylene blue, and phenol as model contaminants was investigated and the charge transfer process was elucidated and compared to that of a TiO2/WO3 heterojunction.

Synthesis and performance evaluation of nanostructured NaFe x Cr1-X (SO4)2 cathode materials in sodium ion batteries (SIBs).

This research work focuses on the synthesis and performance evaluation of NaFe x Cr1-X (SO4)2 (X = 0, 0.8 and 1.0) cathode materials in sodium ion batteries (SIBs). The novel materials having a primary particle size of around 100-200 nm were synthesized through a sol-gel process by reacting stoichiometric amounts of the precursor materials. The structural analysis confirms the formation of crystalline, phase pure materials that adopt a monoclinic crystal structure. Thermal analysis indicates the superior thermal stability of NaFe0.8Cr0.2(SO4)2 when compared to NaFe(SO4)2 and NaCr(SO4)2. Galvanostatic charge/discharge analysis indicates that the intercalation/de-intercalation of a sodium ion (Na+) into/from NaFe(SO4)2 ensues at about 3.2 V due to the Fe2+/Fe3+ active redox couple. Moreover, ex situ XRD analysis confirms that the insertion/de-insertion of sodium into/from the host structure during charging/discharging is accompanied by a reversible single-phase reaction rather than a biphasic reaction. A similar sodium intercalation/de-intercalation mechanism has been noticed in NaFe0.8Cr0.2(SO4)2which has not been reported earlier. The galvanostatic measurements and X-ray photoelectron spectroscopy (XPS) analysis confirm that the Cr2+/Cr3+ redox couple is inactive in NaFe x Cr1-X (SO4)2 (X = 0, 0.8) and thus does not contribute to capacity augmentation. However, suitable carbon coating may lead to activation of the Cr2+/Cr3+ redox couple in these inactive materials.