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New insights into removal efficacy of perfluoroalkyl substances by layered double hydroxide and its composite materials

Though the use of per-and polyfluoroalkyl substances (PFAS) is strictly restricted worldwide, PFAS have been increasingly detected in aqueous environment with high human exposure risk. Effective PFAS remediation requires the simultaneous concentration and decomposition of these compounds from dilute solutions, presenting a significant challenge. The present work evaluated the suitability of layered double hydroxide (LDH) materials, promising adsorbents for anionic pollutants, for the removal of long-chain and short-chain PFAS in micro-polluted water. Additionally, it explored their potential for PFAS degradation after modification. The results suggested that LDH adsorbents have limited ability to extract short-chain PFAS such as perfluorobutane sulfonate (PFBS) from water matrices, especially in dilute solutions. Although organic modification of LDHs could enhance their uptake efficacy on PFAS, it cannot improve the decomposition of PFAS. Innovatively, a composite featuring zero-valent iron (ZVI) particles coupled with LDH was developed, in which the nanoscale ZVI core is coated with LDH to adsorb and decompose perfluorooctanoic acid (PFOA) synergistically. Characterization of the composite showed that LDH coating not only hinders the aggregation of ZVI particles, but also reduces the passivation of ZVI. The PFOA removal efficacy of the composite can be further facilitated in acid environment. By-product analysis revealed that the composite decomposed PFOA mainly through decarboxylation and formation of unstable alcohol.

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Heat and mass transport micropolar Maxwell and Williamson nanofluids flow past a perpendicular cylinder using combined convective flow

The current study aims to investigate the heat and mass transport characteristics of micropolar Maxwell and Williamson nanofluids flowing past a perpendicular cylinder under the influence of combined convective flow using the Buongiorno nanofluid model. The objective is to analyze the axisymmetric flow of these nanofluids around an orthogonal cylinder, highlighting the effects of various physical parameters on temperature profiles and velocity distributions. Maple 23 software was employed to solve the coupled nonlinear differential equations derived from appropriate similarity transformations. The numerical results are presented in tabular and graphical form to show the impacts of key parameters on the selected micropolar nanofluids. The significant outcomes show that the skin friction coefficient, as well as the Nusselt and Sherwood numbers, increase along the axial direction, indicating enhanced heat and mass transfer capabilities. Additionally, the study emphasizes the roles of micro polarity, relaxation time, and viscoelastic properties in modulating these transfer processes. These findings have significant implications for applications in biomechanics, polymer manufacturing, aerosol deposition, and thermal treatment processes, offering valuable insights for future research and industrial practices.

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Understanding the growth kinetics of polydopamine nanoparticles as a function of the temperature and the type of alcohol used as solvent media in their polymerization

Currently, one of the bottlenecks in the large-scale production of particles used for biomedical purposes is reproducibility achieving sizes less than 100 nm. For this reason, the main purpose of this work was to elucidate how the size of polydopamine nanoparticles (PDA NPs), which are widely used in cancer nanomedicine, was affected by several synthesis parameters to facilitate their production scaling-up. Specifically, PDA NPs growth kinetics were investigated as a function of the polymerization temperature (15-50°C) and the type of alcohol (ethanol, 2-propanol, or a mixture of both) used to produce them, finding that an increase in temperature and the amount of 2-propanol in the solvent media allowed smaller NPs to be obtained. Based on the results achieved, a mathematical model capable of predicting PDA NP diameter as a function of the temperature and reaction time, the NH4OH concentration, and the type of alcohol used to synthesize them was proposed. Also, PDA solubility in the different media was studied to explain NP size behavior depending on the type of alcohol employed, which conditioned the formation of PDA oligomers. Finally, additional assays were conducted to confirm that an increase in the synthesis temperature did not affect some of the most important properties of PDA NPs from a biomedical point of view: their Fe3+-loading capacity and their inherent antitumor activity. Therefore, the results obtained in this research could be useful to scale-up the obtaining of 100 nm PDA NPs in a reproducible manner hereafter without significantly altering their outstanding physical-chemical properties.

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A Review on Novel Routes of Synthesizing Titanium Dioxide-Based Nanostructure Derived from Ilmenite Mineral

Nanostructure materials have received significant attention in recent years due to the unique properties and potential applications in various fields. Among these materials, titanium dioxide (TiO2)-based materials have proven promising due to outstanding mechanical, electrical, and catalytic properties. Therefore, this research aimed to offer a comprehensive overview of synthesis and photocatalytic applications of TiO2-based nanostructure materials derived from ilmenite mineral. Furthermore, the pretreatment process of ilmenite mineral using mechanical activation was explored. Various synthetic routes, such as liquid-based, residue-based, and direct ilmenite-based approaches, were also discussed and the advantages and limitations of the routes were explained. In addition, the research included a comparative analysis of the properties of TiO2-based nanostructure materials derived from ilmenite mineral with the commercial in terms of crystallinity, composition, morphology, and selected optical properties. The article concluded with a discussion of the challenges and prospects for using nanostructure materials based on TiO2 from ilmenite mineral. This research served as a valuable resource for explorers and scientists working on nanostructure materials and provides insight into the sustainable use of natural resources for synthesis of advanced TiO2-based materials with shaped properties.

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Accelerated de-chelation of EDTA-metal complexes: A novel and versatile approach for wastewater and solid waste remediation

Industrial waste, including wastewater and solid waste, often contains toxic heavy metals that necessitate extraction and separation prior to safe disposal or reusing them. Sewage sludge incineration ash (SSIA), a non-incinerable waste, holds significant amounts of heavy metals such as iron, zinc, copper, nickel, chromium, and lead. Recovery and reuse of heavy metals from SSIA and further application of treated SSIA sludge remain challenging. Ethylenediaminetetraacetic acid (EDTA) is widely used for heavy metals chelation in different applications. While its chelation with heavy metals is rapid and easy to achieve, the de-chelation of the metal complexes is otherwise slow (∼3 days) and challenging due to their high stability constants. In this study, we investigate the recovery of heavy metals from SSIA through chelation using EDTA, and develop, for the first time, a method to rapidly de-chelate the EDTA-metal complexes through the facile chilling process (1 – 3 h) that accelerates the separation of EDTA and metal ions. A sequential precipitation of high-purity heavy metals from the EDTA-metal complexes was demonstrated with and without de-chelation. This novel and versatile method allows the separation of many valuable compounds from the treated SSIA, including regenerated EDTA, potassium hexafluorosilicate, iron phosphate, iron(III) hydroxide, iron silicate, titanium phosphate, calcium phosphate, copper(I) thiocyanate, nickel bis(dimethylglyoximate), lead(II) sulfate, and zinc sulfide. This approach opens doors for more sustainable waste management and the recovery of valuable resources from industrial waste.

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Enhancing the environmental and economic sustainability of heterotrophic microalgae cultivation: Kinetic modelling and screening of alternative carbon sources

Heterotrophic microalgae cultivation has been suggested to reduce conventional photo-autotrophic microalgal biomass production costs. In heterotrophic cultivation, the most relevant operational costs are constituted by the supply of pure substrates used as carbon source (e.g., glucose), and the high energy request for culture aeration. In addition, suboptimal conditions of temperature and pH reduce the algal productivity, further increasing production costs. In this work, an attempt was made to define more sustainable and cost-effective strategies for the heterotrophic cultivation of Chlorellaceae and Scenedesmaceae. Several by-products from a local confectionery industry were thus screened as alternative carbon sources. Manufacturing residues from peppermint and liquorice candies production allowed to achieve comparable maximum growth rates (1.44 d-1), biomass yields (0.33 g COD·g COD-1) and biomass productivities (370 mg COD·L-1·d-1) as those achieved using glucose. A preliminary economic evaluation showed that the operational costs could be lowered of up to 85.6% by substituting glucose with the selected industrial by-products. As for fermentation conditions, high growth rates could be maintained at relatively low dissolved oxygen (DO) concentrations, and in a large range of temperature and pH values. In addition, optimal temperatures (37.0 – 37.2°C), pH values (6.8 – 7.4), and DO concentrations (> 0.5 – 1 mg O2·L-1) were identified. On the overall, the study demonstrated the possibility of achieving the reduction of operational costs for heterotrophic microalgae cultivation, while implementing circular economy principles in the framework of resource recovery during the bioremediation of organic waste.

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Conversion augmentation of an industrial NH3 oxidation reactor by geometry modification to improve the flow and temperature pattern uniformity using CFD modeling

BackgroundThe optimization of flow and temperature patterns in industrial reactors is crucial for achieving efficient and uniform chemical reactions. This study's major goals are to pinpoint possible areas for improvement in the NH3 oxidation reactor's performance and to deal with the problem of uneven flow distribution inside the reactor. MethodsIn this study, the reactor building design has been changed by extending the feed pipeline vertically and increasing the number of incoming feed streams in order to achieve uniformity in the property distribution on the catalyst surface of an industrial NH3 Oxidation reactor. Thus, using the CFD approach and the finite volume method, a three-dimensional model has been suggested. The results are contrasted with the actual geometrical configuration. The property alteration along the catalyst surface and the reactor length have been assessed. Significant findingsBy expanding the feed pipeline, the flow pattern at the reactor entry is fully developed and becomes uniform. As a result, NO2 production could go up by as much as 11 %. The rates of NH3 conversion, NO yield, and HNO3 generation consequently increased by 12.5 %, 3.1 %, and 8.0 %, respectively. Additionally, this alteration results in a uniform distribution of temperature and pressure across the catalytic surface, prolonging the lifetime of the catalyst. The pressure and temperature difference over the surface of the catalyst with the original reactor configuration was also found to be approximately 250 Pa and 423.15 K, according to the data. Pressure and temperature difference were reduced to 15 Pa and 273.15 K, respectively, as the feed line's length was increased at the same time.

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