Removal of iron and manganese from groundwater sources using nano-biosorbents

Background The presence of iron (Fe) and manganese (Mn) ions in rocky beds leads to groundwater pollution. Moreover, their excessive concentration causes bad taste and color stains of water. Methods Tea leaves-derived char (TLC), rice straw-derived char (RSC), and nanosilica (NS) were used to adsorb Fe and Mn ions from water sources. The effects of parameters such as contact time, composition percentage, and particle size of biosorbents in a fixed-bed adsorption column were investigated. Results The study on the adsorption of Fe and Mn ions showed that the amount of adsorption increased significantly by decreasing the particle size. Furthermore, the combination of nano-biosorbents with nanosilica improved the adsorption. The Thomas and Adams–Bohart models adequately indicated the adsorption of Fe and Mn ions onto nano-biosorbents in the column mode. The TLC and RSC with NS are applicable for the removal of Fe and Mn ions from groundwater. Conclusions According to the BET analysis results, with more crushing of biosorbents by ball mill and placing them in the furnace, specific surface area of tea leaves and rice straw increased from 0.29 to 3.45 and from 3.70 to 10.99 m2/g, respectively. The absorption of iron and manganese from the aqueous solution increased with the percentage of nano-silica. According to breakthrough curves, under best conditions (the seventh mode), nano-biosorbents could remove 98.05% and 97.92% of iron and manganese ions, respectively. The maximum equilibrium capacity of the adsorption column (mg/g) was 256.56 for iron and 244.79 for manganese. Graphical abstract

Photocatalytic degradation of VOCs from air stream using Mo:TiO2/GAC nanocomposites

Modification of TiO2 is one of the techniques used to enhance its photodegradation efficiency and to make it visible-light-active. In this study, Mo-doped TiO2 nanoparticles were synthesized using a fast sol-gel technique, and then coated on granular activated carbon (GAC) as both substrate and adsorbent to obtain Mo:TiO2/GAC composite. The fabricated composite was characterized using powder XRD, SEM, EDAX, FTIR, and BET analysis. Then the composite was applied to photodegrade volatile organic compounds (VOCs) under both UV and visible light irradiation. The characterization results showed high crystallinity and purity. Mo:TiO2/GAC composite had higher photodegradation efficiency compared with bare TiO2 and bare GAC. Moreover, studying operational parameters showed that the optimum condition for photodegradation efficiency of VOCs was at flowrate of 1 l/min, VOCs concentration of 20 ppm, and light intensity of 400 and 600 W/m2 for UV and visible light respectively. The results suggest that Mo:TiO2/GAC is a visible-light-active composite and can be acceptably used to decompose VOCs under visible light with adequate efficiency and without the generation of harmful by-products such as O3 as compared with UV.

Growth of Interconnected ZnO Nanostructures-Its Photocatalytic and Electrochemical Properties

We report the synthesis of interconnected ZnO nano structures through the addition of polyvinyl pyrrolidone (PVP) in a growth medium consisting of ZnCl2 and NaOH at a temperature of 70 0C with a reaction time of 24 hrs. The formation of interconnected ZnO is evaluated in accordance with the reaction time and reaction temperature used for the synthesis, and samples were characterized by powder X-ray diffraction, Fourier transform infra- red (FTIR) spectroscopy, Brunauer-Emmett-Teller(BET) analysis, Field emission scanning electron microscopy (FESEM), Photoluminescence (PL) and Electrochemical methods. BET studies show the mesoporous nature of ZnO grown with the addition of PVP in the growth medium. Interconnected ZnO nanostructures exhibit efficient visible light driven photo catalytic degradation of methylene blue (MB) attributed to interconnected morphology of ZnO. Electro chemical studies have shown that the interconnected ZnO nanostructures give higher order specific capacitance.

A Low Cost Fe3O4–Activated Biochar Electrode Sensor by Resource Utilization of Excess Sludge for Detecting Tetrabromobisphenol A

Owing to its ubiquity in natural water systems and the high toxicity of its accumulation in the human body, it is essential to develop simple and low-cost electrochemical sensors for the determination of 3,3′,5,5′-tetrabromobisphenol A (TBBPA). In this work, Fe3O4–activated biochar, which is based on excess sludge, was prepared and characterized using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR) and BET analysis to analyze its basic features. Subsequently, it was used to fabricate an electrochemical sensor for the detection of TBBPA. The electrochemical test results revealed that the Fe3O4–activated biochar film exhibited a larger active surface area, a lower charge transfer resistance and a higher accumulation efficiency toward TBBPA. Consequently, the peak current of TBBPA was significantly enhanced on the surface of the Fe3O4–activated biochar. The TBBPA sensing platform developed using the Fe3O4–activated biochar composite film, with relatively a lower detection limit (3.2 nM) and a wider linear range (5–1000 nM), was successfully utilized to determine TBBPA levels in water samples. In summary, the effective application of Fe3O4–activated biochar provided eco-friendly and sustainable materials for the development of a desirable high-sensitivity sensor for TBBPA detection.

Highly Photoactive Titanium Dioxide Supported Platinum Catalyst: Synthesis Using Cleaner Ultrasound Approach

Catalysts increase reaction rates; however, the surface area to volume ratio of catalysts has a vital role in catalytic activity. The noble metals such as platinum (Pt) and gold (Au) are expensive; despite this, they have proven their existence in catalysis, motivating the synthesis of supported metal catalysts. Metal catalysts need to be highly dispersed onto the support. In this investigation, an ultrasound approach has been attempted to synthesise highly photoactive titanium dioxide (TiO2) nanoparticles by the hydrolysis of titanium tetraisopropoxide in an acetone/methanol mixture. To enhance its photocatalytic activity, TiO2 was doped with Pt. The synthesised photocatalyst was characterised by techniques such as particle size analysis (PSA), XRD, FE-SEM, TEM, and EDX. The enhancement in the surface characteristics of Pt-doped TiO2 compared with bare TiO2 support was confirmed with Brunauer–Emmett–Teller (BET) analysis. The enhanced surface area and uniformity in particle size distribution at the nanoscale level were due to the effects of ultrasonic irradiation. The obtained results corroborated the size and composition of the synthesised catalysts. The size of the catalysts is in the nanometre range, and good dispersion of Pt catalysts over the TiO2 support was observed. The UV-Visible spectroscopy analysis was performed to study the optical properties of the synthesised TiO2 and Pt/TiO2 photocatalysts. An increase in the absorbance was noted when Pt was added to TiO2, which is due to the decrease in the band gap energy.

Studies on Synthesis and Characterization of Fe3O4@SiO2@Ru Hybrid Magnetic Composites for Reusable Photocatalytic Application

Degradation of dye pollutants by the photocatalytic process has been regarded as the most efficient green method for removal organic dyes from contaminated water. The current research work describes the synthesis of Fe3O4@SiO2@Ru hybrid magnetic composites (HMCs) and their photocatalytic degradation of two azo dye pollutants, methyl orange (MO) and methyl red (MR), under irradiation of visible light. The synthesis of Fe3O4@SiO2@Ru HMCs involves three stages, including synthesis of Fe3O4 magnetic microspheres (MMSs), followed by silica (SiO2) coating to get Fe3O4@SiO2 MMSs, and then incorporation of presynthesized Ru nanoparticles (~3 nm) onto the surface of Fe3O4@SiO2 HMCs. The synthesized HMCs were characterized by XRD, FTIR, TEM, EDS, XPS, BET analysis, UV-DRS, PL spectroscopy, and VSM to study the physical and chemical properties. Furthermore, the narrow band gap energy of the HMC photocatalyst is a significant parameter that provides high photocatalytic properties due to the high light adsorption. The photocatalytic activity of synthesized Fe3O4@SiO2@Ru HMCs was assessed by researching their ability to degrade the aqueous solution of MO and MR dyes under visible radiation, and the influence of various functional parameters on photocatalytic degradation has also been studied. The results indicate that the photocatalytic degradation of MO and MR dyes is more than 90%, and acid media favors better degradation. The probable mechanism of photodegradation of azo dyes by Fe3O4@SiO2@Ru HMC catalysts has been proposed. Furthermore, due to the strong ferromagnetic Fe3O4 core, HMCs were easily separated from the solution after the photocatalytic degradation process for reuse. Also, the photocatalytic activity after six cycles of use is greater than 90%, suggesting the stability of the synthesized Fe3O4@SiO2@Ru HMCs.

Oxygen Vacancies Enable Excellent Electrochemical Kinetics of Carbon Coated Mesoporous SnO2 Nanoparticles in Lithium Ion Battery

Herein, we report the synthesis, characterization and electrochemical performance of carbon coated mesoporous SnO2 nanoparticles (NPs) prepared by adopting a simple hydrothermal process. BET analysis shows that the SnO2 formed...

Microwave-Assisted Hydrothermal Synthesis of Zinc-Aluminum Spinel ZnAl2O4

The drawback of the hydrothermal technique is driven by the fact that it is a time-consuming operation, which greatly impedes its commercial application. To overcome this issue, conventional hydrothermal synthesis can be improved by the implementation of microwaves, which should result in enhanced process kinetics and, at the same time, pure-phase and homogeneous products. In this study, nanometric zinc aluminate (ZnAl2O4) with a spinel structure was obtained by a hydrothermal method using microwave reactor. The average ZnAl2O4 crystallite grain size was calculated from the broadening of XRD lines. In addition, BET analysis was performed to further characterize the as-synthesized particles. The synthesized materials were also subjected to microscopic SEM and TEM observations. Based on the obtained results, we concluded that the grain sizes were in the range of 6–8 nm. The surface areas measured for the samples from the microwave reactor were 215 and 278 m2g−1.

Fabrication and Characterization of Environmentally Friendly Biochar Anode

Electrical power generation by means of electrochemical systems utilizing wastewaters is a global energy challenge tackling technique for which a creation of novel eco-friendly electrode materials is in high relevance. For this purpose a Rhodophyta algae derived activated biochar anode bound with a flaxseeds mucilage binder (5, 10, 20, 30 wt.%) was formed and characterized by thermogravimetric, Brunauer-Emmett-Teller (BET) analysis as well as conductivity and mechanical resistance determination. Activation technique with KOH prior to carbonization at 800 °C of algae was employed to obtain biocarbon with a large surface area. The highest specific surface area of 1298.49 m2/g was obtained with the binder-free sample and had a tendency to decrease with the increase of the binder content. It was estimated that biochar anodes are thermally stable at the temperature of up to 200 °C regardless of binder concentration. The concentration of the binder on the other hand had a significant influence in anodes mechanical resistance and electrical conductance: anode with 30 wt.% of the binder had the highest compressive strength equal to 104 bar; however, the highest conductivity was estimated in anode with 5 wt.% of the binder equal to 58 S/m. It is concluded that anode with 10 wt.% mucilage binder has the optimal properties necessary in MFC utilization.

Bisphenol A Adsorption on Silica Particles Modified with Beta-Cyclodextrins

This study presents the synthesis of silica particles bearing two beta-cyclodextrin (BCD) (beta-cyclodextrin-BCD-OH and diamino butane monosubstituted beta-cyclodextrin-BCD-NH2). The successful synthesis of the BCD-modified silica was confirmed by FT-IR and TGA. Using contact angle measurements, BET analysis and SEM characterization, a possible formation mechanism for the generation of silica particles bearing BCD derivatives on their surface was highlighted. The obtained modified silica displayed the capacity to remove bisphenol A (BPA) from wastewater due to the presence of the BCD moieties on the surface of the silica. The kinetic analysis showed that the adsorption reached equilibrium after 180 min for both materials with qe values of 107 mg BPA/g for SiO2-BCD-OH and 112 mg BPA/g for SiO2-BCD-NH2. The process followed Ho’s pseudo-second-order adsorption model sustaining the presence of adsorption sites with different activities. The fitting of the Freundlich isotherm model on the experimental results was also evaluated, confirming the BCD influence on the materials’ adsorption properties.