Recent advances in the application of magnetic materials for the management of perfluoroalkyl substances in aqueous phases.

Perfluoroalkyl substances (PFASs) are a class of artificially synthesised organic compounds extensively used in both industrial and consumer products owing to their unique characteristics. However, their persistence in the environment and potential risk to health have raised serious global concerns. Therefore, developing effective techniques to identify, eliminate, and degrade these pollutants in water are crucial. Owing to their high surface area, magnetic responsiveness, redox sensitivity, and ease of separation, magnetic materials have been considered for the treatment of PFASs from water in recent years. This review provides a comprehensive overview of the recent use of magnetic materials for the detection, removal, and degradation of PFASs in aqueous solutions. First, the use of magnetic materials for sensitive and precise detection of PFASs is addressed. Second, the adsorption of PFASs using magnetic materials is discussed. Several magnetic materials, including iron oxides, ferrites, and magnetic carbon composites, have been explored as efficient adsorbents for PFASs removal from water. Surface modification, functionalization, and composite fabrication have been employed to improve the adsorption effectiveness and selectivity of magnetic materials for PFASs. The final section of this review focuses on the advanced oxidation for PFASs using magnetic materials. This review suggests that magnetic materials have demonstrated considerable potential for use in various environmental remediation applications, as well as in the treatment of PFASs-contaminated water.

A Novel Metal-Containing Mesoporous Silica Composite for the Decolorization of Rhodamine B: Effect of Metal Content on Structure and Performance.

A series of novel MnxFey@SiO2 (x,y = 1-20%) nanocomposites were synthesized for the first time via the sol-gel/combustion method with different content of precursors (Mn and Fe acetate salts). The effect of precursor content and ratio on physicochemical properties were observed by various characterization methods. Moreover, Rhodamine B (RhB) was chosen as the target pollutant to test the performance of these nanocomposites under a photocatalytic Fenton-like reaction. The results showed that the nanocomposite morphology improved by increasing Fe and Mn content. In this study, interesting behavior was observed in BET results which were different from the fact that increasing metal content can decrease the surface area. This study revealed that one metal could be more critical in controlling the properties than another. Moreover, the precursor ratio appears to have a more tangible effect on the surface area than the effect of precursor content. Among all synthesized nanocomposites, Mn1Fe5@SiO2 showed the highest surface area of 654.95 m2/g. At optimum batch conditions (temp = 25 °C, catalyst dosage = 1 g L-1, H2O2 = 75 mmolL-1, and initial RhB concentration = 50 mg L-1), complete removal (simultaneous adsorption/degradation) occurred using Mn1Fe5@SiO2 at neutral pH. This study showed that the designed nanomaterial could be used as a dual functional adsorbent/photocatalyst in different environmental applications.

Rapid surface degradation of co-axially arranged polypropylene globules by nanoporous carbonized TiO2 assisted with UV-C.

The degradation of plastics, especially polypropylene (PP), is difficult since it is the most hydrophobic polymer. Photocatalytic degradation of PP films has been reported to be one of the most efficient degradation techniques. However, it is still insignificant to employ it in field applications. In this study, TiO2 nanoparticles supported on amorphous carbon with nanoporosity (TiO2@NC) are used as a photocatalyst to degrade macro-sized co-axially oriented PP globules under the influence of UV-C irradiation. Surface characterization such as SEM, ATR-FTIR, and XPS of the PP globules was performed. The SEM images distinctly showed the surface degradation phenomenon. Interestingly, the ATR-FTIR spectra demonstrated a significant rise in the band intensity in the -OH radical region and fairly in the CO region as well, with the increase in the photocatalytic time. Surprisingly, in the XPS spectra, the intensity of C-1s spectra kept on falling, and the intensity of O-1s spectra kept on rising with the increase in the photocatalytic time. The higher surface area due to nanoporosity of TiO2@NC enhanced the photocatalytic degradation of PP globules than previously reported studies. TiO2@NC seems to be a potential catalyst for the degradation of different types of polymers.

Stearic acid mediated growth of edge-on oriented bilayer poly(3-hexylthiophene) Langmuir films.

The growth and structural evolution of stearic acid (SA) blended poly(3-hexylthiophene) [P3HT] Langmuir and Langmuir-Blodgett (LB) films were studied using complimentary surface and interface sensitive techniques to understand the possibility of ordering and layering of promising charge carrier mobility polymers, at the air-water interface and on the transferred solid substrate. SA-induced and subsequent compression-induced transitions in P3HT structure, from aggregated-3D to soft-2D and from in-plane mixed to unmixed layer, are evident at low and high pressures, respectively. The blending of SA molecules enhances the amphiphilic character of P3HT, which reduces the extent of the out-of-plane aggregation to form edge-on oriented (EO) bottom side-chain folded-bilayer (f-BL) islands (of size ~60 nm) within SA monolayer (ML), of commensurate thickness (~2.6 nm). Further compression, gradually rejects the less hydrophilic f-BL islands from the mixed layer to form EO P3HT BL islands (of coverage in-tune with starting composition) on top of SA ML. The formation of nearly covered P3HT(BL)/SA(ML) structured film on solid substrate is evident for the first time, which (even of limited P3HT thickness) has immense importance in the device properties, as the current in the bottom-gated organic thin-film transistors is known to travel only within few ML region near gate-dielectric.

Photocatalytic Degradation of Organic Pollutants over MFe2O4 (M = Co, Ni, Cu, Zn) Nanoparticles at Neutral pH.

In this study, we report a surfactant-mediated synthesis of ferrites (MFe2O4: M = Co, Ni, Cu, Zn) using the co-precipitation-oxidation method. The band gap calculated from UV-Visible diffuse reflectance spectra were found in the range of 1.11-1.81 eV. These ferrite nanocatalysts were studied for the photocatalytic degradation of multiple organic dyes in a 32 W UV-C/H2O2 system. All the four ferrites showed an excellent dye degradation rate in the range of 2.065-2.417 min-1 at neutral pH. In the optimized condition, NiF was found to degrade 89%, 92%, 93%, and 78% of methylene blue, methyl orange, bromo green, and methyl red, respectively within 1 min of UV-irradiation. A 40% TOC removal was recorded after 5 min of degradation reaction, which increased to 60% after 50 min. Mechanism elucidated by scavenger studies and fluorescence spectroscopy revealed that •OH and holes were the primary reactive radicals responsible for the degradation process. Ferrite photocatalysts showed an insignificant performance loss in seven consecutive cycles. The photocatalyst was found efficient in the presence of a high concentration of salts. Thus, it was concluded that these photocatalysts are highly suitable for the remediation of dye-contaminated wastewater.

Role of Fe, Na and Al in Fe-Zeolite-A for adsorption and desorption of phosphate from aqueous solution.

In this study, Fe-Zeolite-A as a phosphate adsorbent was synthesized by incorporating iron into the framework of Zeolite-A using ammonium iron citrate as the Fe3+source. The adsorption (in acidic condition) and desorption of phosphate (in alkaline condition) from an aqueous solution was repetitively performed for 18 times in batch test using Fe-Zeolite-A. The rate of adsorption and desorption of PO43- was much faster (consistently) than any of the reported study so far. The crystalline phase of pristine zeolite changed to amorphous after one adsorption phase and ultimately transformed into a highly amorphous phase after 18 adsorption/desorption cycles. It was due to the formation of more active sites on the surface of the zeolite by a release of atoms, breaking of bonds and deposition of metal and phosphate compounds on the surface (by rigorous acid/base treatment). Increase in active sites enhanced the sorption efficiency of Fe-Zeolite-A. With the help of microscopic and spectroscopic techniques, it was found that Fe3+, Al3+and Na+ metal ions of the Fe-Zeolite-A were involved in the adsorption/desorption of PO43-. Fe3+ ion exhibited ligand exchange mechanism by exchanging OH ions with PO43-. Al3+and Na+ exhibited interactions like precipitation, hydrogen bonding, and diffusion respectively to adsorb PO43-. Fe3+ metal ion dominated over other metal ions by ligand exchange principle, making the sorption process a highly reversible one. The adsorbent showed quantitative adsorption/desorption capacity even after continuous 18 cycles indicating a higher level of reusability.

A delayed eco-epidemiological system with infected prey and predator subject to the weak Allee effect.

We consider a system of delay differential equations to represent predator-prey eco-epidemic dynamics with weak Allee effect in the growth of predator population. The basic aim of the paper is to observe the dynamics of such system under the influence of gestation delay of predator and Allee parameter. We analyze essential mathematical features of the proposed model such as uniform persistence, stability and Hopf-bifurcation at the interior equilibrium point of the system. Global asymptotic stability analysis of the positive equilibrium points by constructing a suitable Lyapunov function for the delayed model is carried out separately. We perform several numerical simulations to illustrate the applicability of the proposed mathematical model and our analytical findings. We observe that the system exhibits chaotic oscillation due to increase of the delay parameter τ. We also observe that there is a threshold of Allee parameter above which the predator population will be washed away from the system.