A hybrid electrocoagulation-biocomposite adsorption system for the decolourization of dye wastewater.

Among the various methods for the removal of azo dye, electrocoagulation is recognized to be highly efficient. However, the process is associated with high operation and maintenance cost, which demands the need for reducing the electrolysis time without compromising the performance efficiency. This can be achieved by adopting hybrid electrocoagulation process with a low-cost but effective process, such as adsorption. The study investigated the performance of a hybrid electrocoagulation-biocomposite system (H-EC-BC) for removing methyl orange dye. Firstly, the operating parameters of electrocoagulation process were optimized and a removal efficiency of 99% has been attained using Fe-SS electrodes at a pH of 6 for a reaction time of 30 min. The performance of EC process was found to be decreasing with increase in dye concentration. Secondly, biocomposite was synthesized from Psidium guajava leaves and characterized using SEM, FTIR, EDAX, and XRD analyses. The results suggested that it is having a porous nature and cellulose crystal structure and confirmed the presence of chemical elements such as carbon (65.2%), oxygen (29.1%) as primary with Fe, Cl, Na and Ca as secondary elements. The performance of the biocomposite was evaluated for the dye adsorption using spectrophotometric methods. Various operating parameters were optimized using experimental methods and a maximum removal efficiency of 65% was achieved at a pH of 6, dosage of 5 g/L and an adsorption contact time of 120 min. The maximum efficiency (92.78%) was obtained with Fe-SS electrodes and KCl as a sustaining electrolyte under acidic circumstances (pH 6). The biocomposite was observed to be more efficient for higher dye concentration. Langmuir and Freundlich adsorption isotherms were fitted with the experimental results with R2 values as 0.926 and 0.980 respectively. The adsorption kinetics were described using Pseudo-first and Pseudo-second order models, wherein Pseudo-second order model fits the experimental results with R2 value of 0.999. The energy consumption of electrocoagulation (EC) process in the hybrid H-EC-BC system was compared to that of a standard EC process. The results demonstrated that the hybrid system is approximately 7 times more energy efficient than the conventional process, thereby implicating its adaptability for field application.

Removal of polystyrene microplastics using biochar-based continuous flow fixed-bed column.

In the realm of environmental challenges, microplastics have emerged as a pressing threat, presenting risks to both individuals and ecosystems. Conventional treatment plants are presently not equipped for effectively removing these minute contaminants. This study presents an investigation into the potential of a continuous flow biochar column, utilizing biochar derived from banana peel through a nitrogen-free slow pyrolysis process for the removal of microplastics. A systematic exploration of various parameters, including bed height, flow rate, inflow microplastic concentration, and microplastic size is undertaken to discern their impact on polystyrene removal efficiency. A peak removal efficiency of 92.16% has been achieved under specific conditions: a 6-cm bed height, a 3-mL/min flow rate, an inlet concentration of 0.05 g/L, and microplastic sizes ranging from 150 to 300 µm. The removal efficiency was inversely affected by flow rate while directly influenced by bed height. To deepen the understanding of polystyrene removal on biochar, a detailed characterization of the synthesized material was carried out. The removal of microplastics by banana peel biochar (BPB) is observed to be dominated by adsorption and filtration processes. The entanglement of microplastics with minuscule biochar granules, capture between particles, and entrapment in the porous system were identified as the mechanisms of removal. Leveraging the hydrophobic nature of polystyrene microplastics, interactions with the hydrophobic functional groups in BPB result in effective adsorption. This is further complemented by self-agglomeration and filtration mechanisms that synergistically contribute to the elimination of larger agglomerates. The findings thus provide a comprehensive understanding, offering hope for a more effective strategy in mitigating the environmental impact of microplastics.

Evaluating the performance of electrocoagulation system in the removal of polystyrene microplastics from water.

Emerging pollutants, particularly microplastics, present a significant threat to both the environment and human health. Traditional treatment methods lack targeted strategies for their removal. This study thoroughly investigated the efficacy of electrocoagulation as a method for efficiently extracting microplastics from water. Various critical operational parameters, including electrode combinations, pH levels, electrolyte concentrations, electrode geometries, configurations, current intensities, and reaction times, were systematically examined. The study systematically examined the impact of different combinations of aluminium (Al) and stainless steel (SS) electrodes, including Al-Al, SS-SS, Al-SS, and SS-Al. Among these combinations, it was found that the Al-Al pairing exhibited outstanding efficiency in microplastic removal, while simultaneously minimizing energy consumption. Initial pH emerged as a critical parameter, with a neutral pH of 7 demonstrating the highest removal efficiency. In the pursuit of optimizing parameters like electrolyte concentrations, electrode geometry, and configuration, it's noteworthy that consistently achieving removal efficiencies exceeding 90% has been a significant achievement. However, to ascertain economic efficiency, additional factors such as energy consumption, electrode usage, and post-treatment conductivity must be taken into account. To tackle the complexity posed by various parameters and criteria, using multi-criteria decision-making tools like TOPSIS is essential, as it has a track record of effectiveness in practical applications. The electrolyte concentration of 0.5 g L-1 is identified as optimal by TOPSIS analysis Additionally, the TOPSIS highlighted the superiority of cylindrical hollow wire mesh electrodes and established the monopolar parallel configuration as the most effective electrode connection method. The investigation carefully evaluated the effect of reaction time, determining that a 50-min window provides optimal microplastic removal efficiency. This refined system exhibited remarkable proficiency in eliminating microplastics of varying size ranges (0-75 µm, 75-150 µm, and 150-300 µm), achieving removal efficiencies of 90.67%, 93.6%, and 94.6%, respectively, at input concentration of 0.2 g L-1. The present study offers a comprehensive framework for optimizing electrocoagulation parameters, presenting a practical and highly effective strategy to address the critical issue of microplastic contamination in aquatic environments.

Coagulation studies on photodegraded and photocatalytically degraded polystyrene microplastics using polyaluminium chloride.

Microplastics are ubiquitous persistent emerging contaminants, and its presence has been detected even in the most pristine and fragile ecosystems. Advanced oxidation processes are one of the novel degradation technologies used for the elimination of microplastics from the environment. In this study, the effect of ultraviolet C (UV-C, 253.7 nm) and ultraviolet A (UV-A, 365 nm) irradiations on polystyrene (PS) microplastic properties in the presence and absence of titanium dioxide were studied along with their coagulation performances using polyaluminium chloride (PAC). The effects of solar irradiation on the chemical properties of microplastics in aqueous and dry conditions were also investigated. PS microplastics (1.5 g) in three size ranges, 300-150 µm, 150-75 µm, and <75 µm were used during this experiment. After 45 days of irradiation, samples showed discolouration, brittleness, and loss of hydrophobicity. Images obtained from scanning electron microscope revealed smoothening and melting of PS surfaces upon UV exposure. Attenuated total reflectance- Fourier transform infrared spectroscopy and X-ray photon spectroscopy of photoaged samples revealed chemical alterations, bond cleavage and formation of oxygenated functional groups on microplastic surfaces. PAC coagulation of samples before and after UV irradiation showed drastic differences in removal efficiencies, with UV-C irradiated microplastics exhibiting maximum efficiency. Large sized and photocatalytically degraded microplastics showed better removal efficiencies than small sized particles. The 300-150 µm sized PS microplastic, degraded photo catalytically under UV-C irradiation showed approximately 99 % removal efficiency, while PS < 75 µm photodegraded under UV-A irradiation showed only 74.2 % removal efficiency.

Methyl orange dye adsorbed biochar as a potential Brønsted acid catalyst for microwave-assisted biodiesel production.

Biodiesel production from non-edible oils utilizing a highly efficient eco-friendly catalyst is a crucial necessity for replacing fossil fuels. In the present work, biochar has been applied for both energy and environmental purposes. The biochar was made by slow pyrolysis from a variety of biomass, primarily cassava peel, irul wood sawdust, and coconut shell. All biochars were used as adsorbents to remove an anionic dye (methyl orange) by conducting batch adsorption studies. The biochar made from cassava peels showed the highest dye adsorption, and it was characterized using elements analysis (CHNS), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), scanning electron microscopy (SEM), surface area analyzer (BET), total acid density, and sulfonic acid group density to successfully confirm the presence of weak (-OH) and strong (-COOH, -SO3H) acidic groups. Furthermore, for microwave-assisted biodiesel production from Millettia pinnata seed oil, the dye adsorbed biochar made from cassava peel was utilized as a Brønsted acid catalyst. The catalyst having a surface area of 4.89 m2/g, an average pore width of 108.77 nm, a total acid density of 3.2 mmol/g, and a sulfonic acid group density of 1.9 mmol/g exhibits distinctive mesoporous properties that contribute to a biodiesel yield of 91.25%. By utilizing the catalyst for three more cycles and getting a yield of more than 75%, the reusability of the catalyst was investigated.