Mugdha S. Bichave

Bio: Mugdha S. Bichave is an academic researcher. The author has contributed to research in topics: Reusability & Nanomaterials. The author has an hindex of 1, co-authored 1 publications receiving 5 citations.

Nano-metal oxides-activated carbons for dyes removal: A review

Abstract: It is common for dyes to be utilized in a wide range of industries such as leather and textiles as well as the printing, paper, and packaging industry. Most dyes fall into a dangerous category of water toxins that have had a significant impact on the ecosystem. Dye removal from wastewater can be done in a variety of methods. It is now necessary to develop advanced and cost-effective methods. Organic dyes may be removed from textiles using adsorption, which is a more effective and environmentally beneficial process. Nanomaterials are a more attractive option for dye removal because of their unique characteristics. An approach to the synthesis, characterization, and dye removal capabilities of nano-metal oxides-activated carbons is presented. This review also includes a discussion of several operating parameters associated with the adsorption process, adsorption isotherms, kinetics, thermodynamic behavior, and reusability of the adsorbent.

Performance of Dye Removal from Single and Binary Component Systems by Adsorption on Composite Hydrogel Beads Derived from Fruits Wastes Entrapped in Natural Polymeric Matrix

Abstract: The treatment of contaminated water is currently a major concern worldwide. This work was directed towards the preparation of a composite hydrogel by entrapping cherry stones powder on chitosan, which is known as one of the most abundant natural polymers. The synthesized material was characterized by scanning electron microscopy, by Fourier transform infrared spectroscopy, and by the point of zero charge determination. Its ability to remove two azo dyes models (Acid Red 66 and Reactive Black 5) existing in single form and in binary mixture was evaluated. Response Surface Methodology–Central Composite Design was used to optimize three parameters affecting the process while targeting the lowest final contaminant concentrations. The best results were obtained at pH 2, an adsorbent dose of 100 g/L, and a temperature of 30 °C, when more than 90% of the pollutants from the single component systems and more than 70% of those of the binary mixtures were removed from their aqueous solutions. The adsorption process was in accordance with Elovich and pseudo-second-order kinetic models, and closely followed the Freundlich and Temkin equilibrium isotherms. The obtained results led to the conclusion that the prepared hydrogel composite possesses the ability to successfully retain the target molecules and that it can be considered as a viable adsorbent material.

Different Adsorption Behaviors and Mechanisms of Anionic Azo Dyes on Polydopamine–Polyethyleneimine Modified Thermoplastic Polyurethane Nanofiber Membranes

Abstract: Considering the notable mechanical properties of thermoplastic polyurethane (TPU), polydopamine–polyethyleneimine (PEI) -modified TPU nanofiber membranes (PDA/PEI-TPU NFMs) have been developed successfully for removal of anionic azo dyes. The adsorption capacity of PDA/PEI-TPU NFMs was evaluated using three anionic dyes: congo red (CR), sunset yellow (SY), and methyl orange (MO). Interestingly, it exhibited different adsorption behaviors and mechanisms of CR on PDA/PEI-TPU NFMs compared with SY and MO. With the decrease in pH, leading to more positive charges on the PDA/PEI-TPU NFMs, the adsorption capacity of SY and MO increased, indicating electrostatic interaction as a main mechanism for SY and MO adsorption. However, wide pH range adaptability and superior adsorption have been observed during the CR adsorption process compared to SY and MO, suggesting a synergistic effect of hydrogen bonding and electrostatic interaction, likely as a critical factor. The adsorption kinetics revealed that chemical interactions predominate in the CR adsorption process, and multiple stages control the adsorption process at the same time. According to the Langmuir model, the maximum adsorption capacity of CR, SY and MO were reached 263, 17 and 23 mg/g, respectively. After six iterations of adsorption–desorption, the adsorption performance of the PDA/PEI-TPU NFMs did not decrease significantly, which indicated that the PDA/PEI-TPU NFMs have a potential application for the removal of CR molecules by adsorption from wastewater.

Efficient and environmentally friendly removal of azo textile dye using a low-cost adsorbent: Kinetic and reuse studies with application to textile effluent

Abstract: Recently, there has been an increasing interest in environmentally friendly methods for the removal of toxic dyes to enable sustainable textile dyeing processes. In this study, a highly efficient, non-toxic, low-cost MgO particles were prepared by sol-gel technique and utilized for the removal of Reactive Red 21 azo dye by adsorption process. The prepared MgO particles were characterized by Scanning Electron Microscopy, Fourier Transform Infrared Spectroscopy, X-Ray Diffraction, and Particle Size Analysis. The batch adsorption studies were performed for optimizing the parameters affecting adsorption. The adsorption behavior of Reactive Red 21 was accurately characterized by the Langmuir model. The adsorption process was found to be thermodynamically spontaneous at room temperatures as indicated by the negative Gibbs free energy change (∆G) value of −30.65 kj/mol. The kinetic studies indicate that the pseudo-second-order model provides a good fit to the adsorption of Reactive Red 21. The adsorption capacity of the prepared MgO particles for Reactive Red 21 was determined to be 355 mg/g at room temperature over a wide pH range of 5–9, with a contact time of 20 min. The regeneration of dye-adsorbed MgO particles was conducted at 500 °C for 2 h. The regenerated MgO particles were then utilized for adsorbing Reactive Red 21 five times with a sufficiently high dye removal efficiency. The prepared MgO particles provided a 98 % dye removal in real textile wastewater containing Reactive Red 21 dye.

Computational insights into the adsorption mechanisms of anionic dyes on the rutile TiO2 (110) surface: Combining SCC-DFT tight binding with quantum chemical and molecular dynamics simulations

Abstract: Metal oxides are gaining momentum rapidly for application in water pollutant remediation. In this study, the adsorption proprieties of two anionic dyes, i.e., acid yellow 36 (AY36) and acid orange 6 (AO6) on the (1 1 0) surface of rutile titanium dioxide (TiO2) in an aqueous medium were investigated using computational methods. The density functional theory (DFT) was used to determine the reactivity of organic molecules by calculating the frontier molecular orbital energies, energy gap (ΔEgap), chemical hardness (η), chemical softness (σ), electronegativity (χ), chemical potential (μ), electrophilicity (ω), the fraction of electrons transferred (ΔN), back-donation energy (ΔEback-donation), Mulliken charge, and Fukui indices. The obtained results showed that the AY36 molecule is more reactive than the AO6 molecule and may have a good adsorption capability compared to the AO6 dye. The most favorable adsorption configurations of AY36 and AO6 molecules were investigated using molecular dynamics (MD) simulation. The calculated interaction energies by MD simulation showed that the TiO2 (1 1 0) surface has a high sensitivity to interact with the two anionic dyes, with more affinity toward the AY36 molecule. Furthermore, to get deep insights into the chemistry of interactions between the anionic dyes and the TiO2 (1 1 0) surface, the self-consistent charge density functional tight-binding (SCC-DFTB) method was carried out. Results showed that anionic dyes adsorbed on the TiO2 (1 1 0) surface by forming covalent bonds between oxygen atoms of the sulfonic group and Ti atoms. Theoretical insights from this work would serve as a guide for researchers to explore the application of oxides in water pollutant remediation.

State-of-the-art adsorption and adsorptive filtration based technologies for the removal of trace elements: A critical review.

Abstract: Water and wastewater are contaminated with various types of trace elements that are released from industrial activities. Their presence, at concentrations above the permissible limit, will cause severe negative impacts on human health and the environment. Due to their cost-effectiveness, simple design, high efficiency, and selectivity, adsorption, and adsorptive filtration are techniques that have received lots of attention as compared to other water treatment techniques. Adsorption isotherms and kinetic studies help to understand the mechanisms of adsorption and adsorption rates, which can be used to develop and optimize different adsorbents. This state-of-the-art review provides and combines the advancements in different conventional and advanced adsorbents, biosorbents, and adsorptive membranes for the removal of trace elements from water streams. Herein, this review discusses the sources of different trace elements and their impact on human health. The review also covers the adsorption technique with a focus on various advanced adsorbents, their adsorption capacities, and adsorption isotherm modeling in detail. In addition, biosorption is critically discussed together with its mechanisms and biosorption isotherms. In the end, the application of various advanced adsorptive membranes is discussed and their comparison with adsorbents and biosorbents is systematically presented.