Sustainable removal of Cr(VI) using graphene oxide-zinc oxide nanohybrid: Adsorption kinetics, isotherms and thermodynamics.

Metal-based adsorbents are limited for hexavalent chromium [Cr(VI)] adsorption from aqueous solutions because of their low adsorption capacities and slow adsorption kinetics. In the present study, decorated zinc oxide (ZnO) nanoparticles (NPs) on graphene oxide (GO) nanoparticles were synthesized via the solvothermal process. The deposition of ZnO NPs on graphene oxide for the nanohybrid (ZnO-GO) improves Cr(VI) mobility in the nanocomposite or nanohybrid, thereby improving the Cr(VI) adsorption kinetics and removal capacity. Surface deposition of ZnO on graphene oxide was characterized through Fourie Transform Infra-red (FTIR), UV-Visible, X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive Spectroscopy (EDS), and Brunauer-Emmett-Teller (BET) techniques. These characterizations suggest the formation of ZnO-GO nanocomposite with a specific area of 32.95 m2/g and pore volume of 0.058 cm2/g. Batch adsorption analysis was carried to evaluate the influence of operational parameters, equilibrium isotherm, adsorption kinetics and thermodynamics. The removal efficiency of Cr(VI) increases with increasing time and adsorbent dosage. FTIR, FESEM and BET analysis before and after the adsorption studies suggest the obvious changes in the surface functionalization and morphology of the ZnO-GO nanocomposites. The removal efficiency increases from high-acidic to neutral pH and continues to decrease under alkaline conditions as well. Mathematical modeling validates that the adsorption follows Langmuir isotherm and fits well with the pseudo 2nd order kinetics (Type 5) model, indicating a homogeneous adsorption process. The thermodynamics study reveals that Cr(VI) adsorption on ZnO-GO is spontaneous, endothermic, and entropy-driven. A negative value of Gibb's Free Energy represents the thermodynamic spontaneity and feasibility of the sorption process. To the best of our knowledge, this is the first study of Cr(VI) removal from aqueous solution using this hybrid nanocomposite at near-neutral pH. The synthesized nanocomposites prove to be excellent candidates for Cr(VI) removal from water bodies and natural wastewater systems.

Adsorption and detoxification of pharmaceutical compounds from wastewater using nanomaterials: A review on mechanism, kinetics, valorization and circular economy.

Antibiotics overuse, inappropriate conduct, and discharge have led to adverse effects on various ecosystems. The occurrence of antibiotics in surface and drinking water is a matter of global concern. It is responsible for multiple disorders, including disruption of endocrine hormones and high chronic toxicity. The hospitals, pharmaceutical industries, households, cattle farms, and aquaculture are the primary discharging sources of antibiotics into the environment. This review provides complete detail on applying different nanomaterials or nanoparticles for the efficient removal of antibiotics from the diverse ecosystem with a broader perspective. Efforts have been made to focus on the degradation pathways and mechanism of antibiotic degradation using nanomaterials. More light has been shed on applying nanostructures in photocatalysis, which would be an economical and efficient solution. The nanoscale material or nanoparticles have incredible potential for mineralizing pharmaceutical compounds in aqueous solutions at low cost, easy handling characteristics, and high efficacy. Furthermore, nanoparticles can absorb the pharmaceutical by-products and wastes at a minimum cost as they can be easily recycled. With the increasing number of research in this direction, the valorization of pharmaceutical wastes and by-products will continue to expand as we progress from old conventional approaches towards nanotechnology. The utilization of nanomaterials in pharmaceutical wastewater remediation is discussed with a major focus on valorization, energy generation, and minimization and its role in the circular economy creating sustainable development.

Biological degradation of polyethylene terephthalate by rhizobacteria.

In view of the growing demand for plastic products, an enormous proportion of plastic waste causing the biological issue is produced. Plants in collaboration with their rhizobacteria partners are also exposed to these contaminants. The study aims to determine the rhizobacterial ability to biodegrade PET plastic. We isolated the rhizobacteria capable of degrading the PET plastic in minimal salt media using it as a sole carbon source. The three rhizospheric isolates, namely Priestia aryabhattai VT 3.12 (GenBank accession No. OK135732.1), Bacillus pseudomycoides VT 3.15 (GenBank accession No. OK135733.1), and Bacillus pumilus VT 3.16 (GenBank accession No. OK1357324.1), showed the highest degradation percentage for PET sheet and powder. The biodegradation end products post 28 days for PET sheet and 18 days of PET powder were studied by Fourier transform infrared spectroscopy (FTIR), high-performance liquid chromatography (HPLC), and scanning electron microscopy (SEM). Our results showed significant biodegradation of PET plastic, and the rate of degradation could account for over 65%. The present study proves soil rhizobacteria's potential and capabilities for efficient degradation of PET plastic occurring at the waste sites. It also implies that rhizobacteria could be beneficial in the remediation of PET waste in future applications.

Multifunctional nanohybrid for simultaneous detection and removal of Arsenic(III) from aqueous solutions.

Herein, for the adsorption and detection of As (III), multifunctional nanohybrid have been synthesized using a solvothermal approach. Structural and functional characterizations confirmed the impregnation of the ZnO over graphene oxide. Nanohybrid exhibits a remarkable qmax (maximum adsorption capacity) of 8.17 mg/g, at an adsorbent dose of 3 g/L and pH of 8.23. Higher adsorption with nanohybrid was attributed to a large BET surface area of 32.950 m2/g. The chemical nature and adsorption behaviour of As(III) on ZnO-GO were studied by fitting the data with various adsorption isotherms (Langmuir & Freundlich) and kinetics models (six models). It is observed from the findings that removal of As(III) with ZnO-GO nanocomposite appears to be technically feasible with high removal efficiency. The feasibility of the nanocomposite to function as a sensor for the detection of As(III) was also evaluated. The fabricated sensor could detect As(III) with a lower limit of detection of 0.24 µM and linear range up to 80 µM. Overall, this study is significant in nanohybrid as a multifunctional composite for the adsorption and detection of As (III) from wastewater.

Study of nano cellulose-based membrane tailorable biodegradability for use in the packaging application of electronic devices.

With a growing demand for packaging materials and witnessing many landfills and huge garbage islands floating in the Pacific oceans, the need for an alternative material such as bio-degradable plastics has risen. Cellulose-based materials are already in use in several packaging industries. Nanocellulose, a processed cellulose with a specific nanostructure, have several advantages such as high specific strength, modulus, high surface area and unique optical properties. By varying the crosslinking percentages, the kinetics of degradation can be tailored. In this work, extracted cellulose from sugarcane bagasse was hydrolyzed to obtain nanocellulose, which was used to fabricate packaging films (membrane) with PVA as matrix and nanocellulose. Variations of PVA and nanocellulose loadings, and crosslinking agent ratios. In the fabricated films were investigated for chemical, mechanical, optical, thermal, and topographical properties. Results from the degradation tests under appropriate physically simulated environments have suggested that the crosslinking has enhanced the mechanical properties, extent of degradation was dependent on percentages of crosslinking. A real-world device packaging application was demonstrated by encapsulation of perovskite solar cells with the fabricated nanocellulose film revealed that the lifetime of the devices improved which might be indicative of the film having lower permeability for oxygen and moisture.

A novel CaO nanocomposite cross linked graphene oxide for Cr(VI) removal and sensing from wastewater.

A novel green nanocomposite has been prepared by immobilizing CaO nanoparticles (CaO NPs) on the surface of graphene oxide. Biogenic CaO-NPs were synthesized from Lala clamshells. Morphological and structural characterizations of the nanocomposite were studied extensively. The adsorption capacity (qmax) of the nanocomposite for removing Cr(VI) was 38.04 mg g-1. In addition to this, the adsorption data were adequately simulated with Langmuir, Freundlich, Temkin, and pseudo-second-order models, suggesting that the adsorption process was the combination of external mass transfer and chemisorption. Electrostatic interaction was the dominant mechanism for Cr(VI) removal. In addition, the synthesized nanocomposites also serve as an excellent sensor for Cr(VI) sensing, with a limit of detection (LOD) of 0.02 µM utilizing electrochemical methods. Therefore, this green nanocomposite can simultaneously serve as an adsorbent and sensor for Cr(VI)removal from aqueous solutions.