Design and Application of Microfluidic Capture Device for Physical-Magnetic Isolation of MCF-7 Circulating Tumor Cells.

Circulating tumor cells (CTCs) are a type of cancer cell that spreads from the main tumor to the bloodstream, and they are often the most important among the various entities that can be isolated from the blood. For the diagnosis of cancer, conventional biopsies are often invasive and unreliable, whereas a liquid biopsy, which isolates the affected item from blood or lymph fluid, is a less invasive and effective diagnostic technique. Microfluidic technologies offer a suitable channel for conducting liquid biopsies, and this technology is utilized to extract CTCs in a microfluidic chip by physical and bio-affinity-based techniques. This effort uses functionalized magnetic nanoparticles (MNPs) in a unique microfluidic chip to collect CTCs using a hybrid (physical and bio-affinity-based/guided magnetic) capturing approach with a high capture rate. Accordingly, folic acid-functionalized Fe3O4 nanoparticles have been used to capture MCF-7 (breast cancer) CTCs with capture efficiencies reaching up to 95% at a 10 µL/min flow rate. Moreover, studies have been conducted to support this claim, including simulation and biomimetic investigations.

Design of low-cost natural casein biopolymer based adsorbent for efficient adsorption of multiple anionic dyes and diclofenac sodium from aqueous solutions.

The treatment of various organic pollutants from industrial wastewater using bio-based materials has gained significant attention owing to their excellent properties such as low-cost, eco-friendly, non-toxic, and biodegradability. In this perspective, casein (Cn), a protein-based biopolymer, was extracted from the cow milk as a low-cost adsorbent, and the adsorption performances were determined for the pristine Cn. The adsorbent was employed for the removal of two different classes of targeted pollutant anionic dyes such as Congo red (CR), Eriochrome Black T (EBT), Eosin Y (EY), and pharmaceutical waste i.e., diclofenac sodium (DS) and displayed better adsorption performances with the maximum adsorption capacity of 85.54, 31.72, 70.42 and 358.42 mg g-1 respectively. The interactions between Cn and pollutants are mainly ascribed to the electrostatic interaction, hydrogen bonding, hydrophobic interaction, and π-π interactions. Furthermore, to validate with realistic application the adsorbent proved with an excellent removal efficiency of 91.43% for fabric whitener i.e., Ujala Supreme®. These obtained results suggest that the Cn could be the potential adsorbent to effectively eliminate toxic pollutants from the aqueous solutions.

Rhodamine 6G derivative for the selective copper detection and remediation using nanoporous diatomaceous earth-engineered functional receptor.

A rhodamine-derived receptor was synthesized and comprehensively characterized for structural confirmation. The receptor was able to distinguish the copper ions (Cu2+) from other competing cations. The yellow color of the receptor changed to pink upon adding Cu2+ ions, however, other competing cations ions were impotent towards any color variation. The UV-visible titration studies revealed the binding stoichiometry of a 1:1 ratio with a detection limit of 9.663 × 10-8 M. Additionally, a novel idea of the work resides in the use of diatom for the practical application, where the receptor has been tethered on nanoporous diatomaceous earth microparticles (P2D) to remove Cu2+ ions. The results confirmed that 50 mg receptor functionalized DE could adsorb 10 mL of 1 ppm Cu2+ ions from water. Furthermore, a proof-of-concept device that is inexpensive, simple to operate, and continuously removes Cu2+ ions from water has been developed. The efficiency of the device in Cu2+ ion removal could be realized through the naked eye by observing the color change of P2D particles, which has excellent potential for application in remote locations where water contamination is a significant issue.

Nanoarchitectonics of Bimetallic MOF@Lab-Grade Flexible Filter Papers: An Approach Towards Real-Time Water Decontamination and Circular Economy.

This study presents a novel approach to decontaminate ferrocyanide-contaminated wastewater. The work effectively demonstrates the use of bimetallic Mo/Zr-UiO-66 as a super-adsorbent for rapid sequestration of Prussian blue, a frequently found iron complex in cyanide-contaminated soils/groundwater. The exceptional performance of Mo/Zr-UiO-66 is attributed to the insertion of secondary metallic sites, which deliver synergistic effects, benefiting the inherent qualities of the framework. Moreover, to extend the industrial applications of metal-organic frameworks (MOFs) in real-world scenarios, an approach is delivered to structure the nanocrystalline powders into MOF-based macrostructures. The work demonstrates an interfacial process to develop continuous MOF nanostructures on ordinary laboratory-grade filter papers. The novelty of the work lies in the development of robust free-standing filtration materials to purify PB dye-contaminated water. Additionally, the work embraces a circular economy concept to address problems related to resource scarcity, excessive waste production, and maintenance of economic benefits. Consequently, the PB dye-loaded adsorbent waste is re-employed for the adsorption of heavy metals (Pb2+ and Cd2+ ). Simultaneously, the study aims to address the problems related to the real-time handling of powdered adsorbents, and the generation of ecologically harmful secondary waste, thereby, progressing toward a more sustainable system.

Microfluidic-Assisted Synthesis of Metal-Organic Framework -Alginate Micro-Particles for Sustained Drug Delivery.

Drug delivery systems (DDS) are continuously being explored since humans are facing more numerous complicated diseases than ever before. These systems can preserve the drug's functionality and improve its efficacy until the drug is delivered to a specific site within the body. One of the least used materials for this purpose are metal-organic frameworks (MOFs). MOFs possess many properties, including their high surface area and the possibility for the addition of functional surface moieties, that make them ideal drug delivery vehicles. Such properties can be further improved by combining different materials (such as metals or ligands) and utilizing various synthesis techniques. In this work, the microfluidic technique is used to synthesize Zeolitic Imidazole Framework-67 (ZIF-67) containing cobalt ions as well as its bimetallic variant with cobalt and zinc as ZnZIF-67 to be subsequently loaded with diclofenac sodium and incorporated into sodium alginate beads for sustained drug delivery. This study shows the utilization of a microfluidic approach to synthesize MOF variants. Furthermore, these MOFs were incorporated into a biopolymer (sodium alginate) to produce a reliable DDS which can perform sustained drug releases for up to 6 days (for 90% of the full amount released), whereas MOFs without the biopolymer showed sudden release within the first day.

Facilitated Adsorption of Mercury(II) and Chromium(VI) Ions over Functionalized Carbon Nanotubes.

By considering the importance of water and its purity, herein, a powerful adsorbent has been developed for the adsorption of two toxic contaminants that commonly exist in water, viz., divalent mercury and hexavalent chromium. The efficient adsorbent, CNTs-PLA-Pd, was prepared by covalent grafting polylactic acid to carbon nanotubes and subsequent deposition of palladium nanoparticles. The CNTs-PLA-Pd could adsorb Hg(II), and Cr(VI) entirely exists in water. The adsorption rate for Hg(II) and Cr(VI) was rapid at initial stage, followed by gradual decrease, and attained the equilibrium. The Hg(II) and Cr(VI) adsorption was perceived within 50 min and 80 min, respectively with CNTs-PLA-Pd,. Further, experimental data for Hg(II) and Cr(VI) adsorption was analyzed, and kinetic parameters were estimated using pseudo-first and second-order models. The adsorption process of Hg(II) and Cr(VI) followed the pseudo-second-order kinetics, and the rate-limiting step in the adsorption was chemisorption. The Weber-Morris intraparticle pore diffusion model revealed that the Hg(II) and Cr(VI) adsorption over CNTs-PLA-Pd occurs through multiple phases. The experimental equilibrium parameters for the Hg(II) and Cr(VI) adsorption were estimated by Langmuir, Freundlich, and Temkin isotherms models. All three models were well suited and demonstrated that Hg(II) and Cr(VI) adsorption over CNTs-PLA-Pd transpires through monolayer molecular covering and chemisorption.

Ratiometric colorimetric detection of fluoride ions using a schiff base sensor: enhancing selectivity and sensitivity for naked-eye analysis.

A Schiff base receptor with an active -NH group was designed and synthesized for the selective and sensitive colorimetric detection of inorganic fluoride (F-) ions in an aqueous medium. The sensitivity of the receptor for F- ions was enhanced by the influence of two electron-withdrawing -NO2 groups at ortho and para positions which result in a vivid color change. The receptor underwent a remarkable color change from light yellow to violet, enabling naked-eye detection of F- ions without the need for spectroscopic equipment. To ensure the structural integrity of the synthesized receptors, prominent spectroscopic techniques such as 1H NMR, FTIR, and GCMS analysis were used for characterization. With a limit of detection (LoD) of 0.0996 ppm, a 1 : 2 stoichiometric binding ratio was observed for receptor and F- ions. The binding mechanism confirmed the deprotonation of the -NH group followed by the formation of -HF2, resulting in an intramolecular charge transfer (ICT) transition, which correlates with UV-vis and 1H NMR titration results. In addition, the proposed binding mechanism of F- ion interaction with the receptor was theoretically validated using DFT and TDDFT calculations. Furthermore, as a real-life implementation of the receptor, quantification of the F- ions present in a commercially available mouthwash was demonstrated. To assess the sensitivity performance, a paper-based dip sensor and a solid substrate sensor by functionalizing the receptor on diatomaceous earth were demonstrated. Finally, sensors were built into smartphones that could recognize the red, green, and blue percentages (RGB%) where each parameter defines the intensity of the color, which could also be used as a supplement to the colorimetric investigations.

Cost effective porous areca nut carbon nanospheres for adsorptive removal of dyes and their binary mixtures.

Novel porous nanospheres from areca nuts (ACNPs) were synthesized via one-step pyrolysis without the use of any chemical treatment and the materials were used as adsorbents for the removal of cationic methylene blue (MB) and anionic methyl orange (MO) as well as their binary mixtures. Around, 6-7 tonnes of areca nut biowaste is generated every year which are then burnt due to their slow rate of decomposition resulting in higher carbon footprints. Biosorbents are generally a preferable alternative for dye adsorption but involve chemical modification for surface enhancement and complex sample treatment. In this work, ACNPs, were investigated for their efficiency in the raw form and were characterized by SEM, EDS, FTIR, XRD, and BET techniques before and after subjecting to the dye adsorption studies. The BET analysis of the adsorbents showed a high specific surface area of 693.8 m2/g when prepared at 1000 °C, while the N2 adsorption-desorption plot showed type-IV isotherm, suggesting the microporous nature of the carbon matrix. Batch equilibrium studies showed the removal efficiency of >95% for both the dyes and their binary mixtures under the optimum conditions of 0.15 g/L dosage, 10 µM concentration and contact time of 70 min. Due to the synergistic effects of the binary dyes, higher removal efficiency of MB compared to MO was observed in the binary mixture. Adsorption results were tested using Langmuir, Freundlich, Temkin, Redlich-Peterson, and Elovich isotherms to assess the best fit of the models. The qm value of MB was found to be 97.37 mg/g, while that of MO was 71.22 mg/g which is higher compared to individual dye components having lower values of 86.12 mg/g and 50.35 mg/g, respectively. Extended Langmuir and Jain and Snoeyink isotherms were used for binary data interpretation. The kinetic results showed good agreement with the Pseudo-second order equation, indicating internal diffusion. The possible mechanism involved electrostatic and á´¨-á´¨ interactions between the dye molecules and ACNPs. This approach is comprehensible and cost effective and can be utilized for dye removal in textile industries.

Efficient separation of arsenic species of oxyanion As (III) and As (V) by using effective polymer inclusion membranes (PIM).

The heavy metal contaminant arsenic exist in the form of arsenite (As(III)) and arsenate (As(V)) ions. These ions are highly carcinogenic that are usually present in the ground water. To date, most of the designed polymer inclusion membrane (PIM) involved only about separation without differentiating the oxidation states. Thus, there is a research gap on separation of element with different oxidation states. Thus, this study addresses such research gap which have been not explored previously. To extract such ions from water, the present study involves fabrication of PIM by varying the compositions of the base polymer, carrier and plasticizer. Also effect of the strip solution, and transport properties were studied. High performance membrane was obtained with 50% (w/w) Aliquat 336 and 50% (w/w) Cellulose triacetate (CTA). The production of 1 m2 of PIM may cost approximately 0.08-0.16$. Also, we have combined the separation capacity of polymer inclusion membrane (PIM) with the sensitivity and elemental detection using atomic absorption spectrometry (AAS) to detect and separate As(III) and As(V). AAS is limited to detecting only elemental arsenic (As) and does not distinguish between As(III) and As(V). Further, to address such limitations in this current study we were able to separate As(V) from As(III) within 5 h. In addition, to provide sole solution a device was fabricated to extract As(V) in the field studies which displayed outstanding efficiency of 99.7 ± 0.2%. The extracted samples was tested in AAS to differentiate between oxidation states of the arsenic species and these important results are supportive in finding out the redox potential of water and for other geochemical explorations.

Elevated Adsorption of Lead and Arsenic over Silver Nanoparticles Deposited on Poly(amidoamine) Grafted Carbon Nanotubes.

An efficient adsorbent, CNTs-PAMAM-Ag, was prepared by grafting fourth-generation aromatic poly(amidoamine) (PAMAM) to carbon nanotubes (CNTs) and successive deposition of Ag nanoparticles. The FT-IR, XRD, TEM and XPS results confirmed the successful grafting of PAMAM onto CNTs and deposition of Ag nanoparticles. The absorption efficiency of CNTs-PAMAM-Ag was evaluated by estimating the adsorption of two toxic contaminants in water, viz., Pb(II) and As(III). Using CNTs-PAMAM-Ag, about 99 and 76% of Pb(II) and As(III) adsorption, respectively, were attained within 15 min. The controlling mechanisms for Pb(II) and As(III) adsorption dynamics were revealed by applying pseudo-first and second-order kinetic models. The pseudo-second-order kinetic model followed the adsorption of Pb(II) and As(III). Therefore, the incidence of chemisorption through sharing or exchanging electrons between Pb(II) or As(III) ions and CNTs-PAMAM-Ag could be the rate-controlling step in the adsorption process. Further, the Weber-Morris intraparticle pore diffusion model was employed to find the reaction pathways and the rate-controlling step in the adsorption. It revealed that intraparticle diffusion was not a rate-controlling step in the adsorption of Pb(II) and As(III); instead, it was controlled by both intraparticle diffusion and the boundary layer effect. The adsorption equilibrium was evaluated using the Langmuir, Freundlich, and Temkin isotherm models. The kinetic data of Pb(II) and As(III) adsorption was adequately fitted to the Langmuir isotherm model compared to the Freundlich and Temkin models.

A comprehensive review on water remediation using UiO-66 MOFs and their derivatives.

Metal-organic frameworks (MOFs) are a versatile class of porous materials offering unprecedented scope for chemical and structural tunability. On account of their synthetic versatility, tunable and exceptional host-guest chemistry they are widely utilized in many prominent water remediation techniques. However, some of the MOFs present low structural stabilities specifically in aqueous and harsh chemical conditions which impedes their potential application in the field. Among the currently explored MOFs, UiO-66 exhibits structural robustness and has gained immense scientific popularity. Built with a zirconium-terephthalate framework, the strong Zr-O bond coordination contributes to its stability in aqueous, chemical, and thermal conditions. Moreover, other exceptional features such as high surface area and uniform pore size add to the grand arena of porous nanomaterials. As a result of its stable nature, UiO-66 offers relaxed admittance towards various functionalization, including synthetic and post-synthetic modifications. Consequently, the adsorptive properties of these highly stable frameworks have been modulated by the addition of various functionalities. Moreover, due to the presence of catalytically active sites, the use of UiO-66 has also been extended towards the degradation of pollutants. Furthermore, to solve the practical handling issues of the crystalline powdered forms, UiO-66 has been incorporated into various membrane supports. The incorporation of UiO-66 in various matrices has enhanced the rejection, permeate flux, and anti-fouling properties of membranes. The combination of such exceptional characteristics of UiO-66 MOF has expanded its scope in targeted purification techniques. Subsequently, this review highlights the role of UiO-66 in major water purification techniques such as adsorption, photocatalytic degradation, and membrane separation. This comprehensive review is expected to shed light on the existing developments and guide the inexhaustible futuristic scope of UiO-66 MOF.

Recent Advances in Microfluidic Platform for Physical and Immunological Detection and Capture of Circulating Tumor Cells.

CTCs (circulating tumor cells) are well-known for their use in clinical trials for tumor diagnosis. Capturing and isolating these CTCs from whole blood samples has enormous benefits in cancer diagnosis and treatment. In general, various approaches are being used to separate malignant cells, including immunomagnets, macroscale filters, centrifuges, dielectrophoresis, and immunological approaches. These procedures, on the other hand, are time-consuming and necessitate multiple high-level operational protocols. In addition, considering their low efficiency and throughput, the processes of capturing and isolating CTCs face tremendous challenges. Meanwhile, recent advances in microfluidic devices promise unprecedented advantages for capturing and isolating CTCs with greater efficiency, sensitivity, selectivity and accuracy. In this regard, this review article focuses primarily on the various fabrication methodologies involved in microfluidic devices and techniques specifically used to capture and isolate CTCs using various physical and biological methods as well as their conceptual ideas, advantages and disadvantages.

Garlic peel based mesoporous carbon nanospheres for an effective removal of malachite green dye from aqueous solutions: Detailed isotherms and kinetics.

Biowaste based nanoadsorbents have gained much attention in the recent times for wastewater decolourization owing to their low cost, high surface area and high adsorption capacities. In the present research, garlic peel based nanoparticles (GCNP) were synthesized at different temperatures by a one step pyrolytic green approach for the effective removal of cationic dye, malachite green from the aqueous medium. The surface properties of Garlic nanoparticles were elucidated by N2 adsorption- desorption and all the GCNP samples were found to exhibit Type IV(a) isotherm indicating the presence of mesopores in carbon matrix. Using BET calculations, highest surface area (380 m2/g) was obtained for GCNP synthesized at 1000 ◦C. Characterization of nanoparticles was done by XRD, EDAX, SEM and FTIR studies before and after the dye treatment. Adsorption studies conducted using different parameters like contact time, concentration and pH and dosage of adsorbent showed removal efficiency above 90% for the contact time of 70 min. Best adsorption experimental results were obtained for GCNP synthesized at 1000 °C ascribable to its high surface area, higher total pore volume (0.26 cm2/g) and higher carbon content. Four adsorption isotherm models were used to validate batch equillibrium studies and the results showed data in good agreement with Langmuir and Freundlich isotherms with maximum Langmuir adsorbtion capactiy to be 373.7 mg/g. Kinetic modelling of the data showed best fit with the Pseudo second order model with rate constant value of 48.726 g mg-1 min-1. Regenerative studies were conducted conducted upto 6 cycles. Also the GC nanoparticles were tested for their compatibility in membrane form wherein, removal efficiency results were obtained for GCNP anchored in polyvinyl difluoride (PVDF) and polysulfone (PSF) membrane matrix for dye adsorption.

Surface engineering of silica based materials with Ni-Fe layered double hydroxide for the efficient removal of methyl orange: Isotherms, kinetics, mechanism and high selectivity studies.

Herein, low-cost diatomite (DE) and bentonite (BE) materials were surface modified with Ni-Fe layered double hydroxide (LDHs) (represented as NFD and NFB respectively), using a simple co-precipitation procedure for the removal of methyl orange (MO) dye from water. The adsorbents of both before and after MO adsorption have been studied by XRD, N2 adsorption-desorption isotherm, FTIR, FESEM-EDX and XPS characterization. The zeta potential analysis was used to observe the surface charge of adsorbents within the pH ranges of 4-10. The MO removal efficiency was significantly improved after LDHs modification, showing a 94.7% and 92.6% efficiency for NFD and NFB at pH 6, respectively. Whereas bare DE and BE have shown removal efficiency of 15.5% and 4.9% respectively. The maximum adsorption capacities of NFD and NFB using the Langmuir isotherm model were found to be 246.9 mgg-1 and 215.9 mgg-1 respectively. The designed NFD showed high selectivity towards anionic-based dyes from water and also the effect of salts shows the dye removal percentage was increased and decreased for the addition of Na2SO4 and NaCl, respectively. The reusability of NFD and NFB have been studied for a maximum of five cycles and they can remove MO up to four cycles. Therefore, the designed adsorbents can be very effective towards the removal of MO from water and they may be useful for dye-based wastewater treatment.

Functionalized Porous Hydroxyapatite Scaffolds for Tissue Engineering Applications: A Focused Review.

Biomaterials have been widely used in tissue engineering applications at an increasing rate in recent years. The increased clinical demand for safe scaffolds, as well as the diversity and availability of biomaterials, has sparked rapid interest in fabricating diverse scaffolds to make significant progress in tissue engineering. Hydroxyapatite (HAP) has drawn substantial attention in recent years owing to its excellent physical, chemical, and biological properties and facile adaptable surface functionalization with other innumerable essential materials. This focused review spotlights a brief introduction on HAP, scope, a historical outline, basic structural features/properties, various synthetic strategies, and their scientific applications concentrating on functionalized HAP in the diverse area of tissue engineering fields such as bone, skin, periodontal, bone tissue fixation, cartilage, blood vessel, liver, tendon/ligament, and corneal are emphasized. Besides clinical translation aspects, the future challenges and prospects of HAP based biomaterials involved in tissue engineering are also discussed. Furthermore, it is expected that researchers may find this review expedient in gaining an overall understanding of the latest advancement of HAP based biomaterials.

Cerium based UiO-66 MOF as a multipollutant adsorbent for universal water purification.

Herein, we demonstrate the use of cerium (Ce)-UiO-66 metal organic framework (MOF) for the removal of a variety of potentially toxic pollutants. The Ce-UiO-66 MOF, with similar framework topologies to Zr-UiO-66, has not been explored for its adsorptive properties in water remediation. The replacement of Zr metal center with Ce yields a MOF that can be synthesized in shorter durations with lesser energy consumptions and with excellent multipollutant adsorption properties. Further, the Ce-UiO-66 MOF was also studied for its adsorption abilities in the binary component system. Interestingly, the adsorbent showed higher adsorption capacities in the presence of other pollutants. Removal studies for other potentially toxic anionic and cationic dyes showed that the Ce-UiO-66 MOF has a wide range of contaminant removal abilities. Investigations of individual adsorption capacities revealed that the Ce-UiO-66 MOF has a maximum adsorption capacity of 793.7 mg/g for congo red (CR), 110 mg/g for methylene blue (MB), 66.1 mg/g for fluoride (F-), 30 mg/g for Cr6+ and 485.4 mg/g for the pharmaceutical waste diclofenac sodium (DCF). To imply the practical applications of the Ce-UiO-66 MOF we have also demonstrated an adaptable filter that could separate all the potentially toxic pollutants.

New optofluidic based lab-on-a-chip device for the real-time fluoride analysis.

A PDMS (Polydimethylsiloxane) microfluidic channel coupled with UV-vis fibre-optic spectrometer and new synthesized colorimetric probe was integrated into an optofluidic based Lab-on-a-chip device for highly sensitive and real-time quantitative measurements of fluoride ions (F¯). An 'S' shaped microchannel in a microfluidic device was designed to act as microreactor to facilitate the continuous reaction between synthetized colorimetric probe (sensor) and F¯ ions. Following this reaction, the UV-vis optical probe in the downstream detection zone of the microfluidic device was used to capture their spectrum and present as F¯ concentration in real-time conditions. An initial study of the developed colorimetric probe with multi-colour change with several binding and chromophore groups such as -OH, -NH and -NO2 groups confirmed its high sensitivity and selectivity for F¯ ions with a detection limit of 0.79 ppm. The performance of the developed optofluidic device was evaluated for the selective, sensitive detection of F¯ ions including real samples out-performing conventional methods. The technology has advantages such as low sample consumption, rapid analysis, high sensitivity and portability. Presented new Lab-on-a-chip device provides many competitive advantages for the real-time analysis of F¯ ions needed across broad sectors.

MOF based engineered materials in water remediation: Recent trends.

The significant upsurge in the demand for freshwater has prompted various developments towards water sustainability. In this context, several materials have gained remarkable interest for the removal of emerging contaminants from various freshwater sources. Among the currently investigated materials for water treatment, metal organic frameworks (MOFs), a developing class of porous materials, have provided excellent platforms for the separation of several pollutants from water. The structural modularity and the striking chemical/physical properties of MOFs have provided more room for target-specific environmental applications. However, MOFs limit their practical applications in water treatment due to poor processability issues of the intrinsically fragile and powdered crystalline forms. Nevertheless, growing efforts are recognized to impart macroscopic shapability to render easy handling shapes for real-time industrial applications. Furthermore, efforts have been devoted to improve the stabilities of MOFs that are subjected to fragile collapse in aqueous environments expanding their use in water treatment. Advances made in MOF based material design have headed towards the use of MOF based aerogels/hydrogels, MOF derived carbons (MDCs), hydrophobic MOFs and magnetic framework composites (MFCs) to remediate water from contaminants and for the separation of oils from water. This review is intended to highlight some of the recent trends followed in MOF based material engineering towards effective water regeneration.

Recovery of spent VOSO4 using an organic ligand for vanadium redox flow battery applications.

To recover the spent vanadium compound, Rhodamine-B-based Schiff's base ligand (L1) was synthesized via ultrasonication process and was evaluated with vanadyl sulfate (VOSO4), which has shown considerable selectivity towards V(IV). The change of the solution color from colorless to pink is attributed to L1 after the reaction with vanadium ion owing to the successful formation of the vanadium complex and the opening of the spirolactam ring in the L1 structure. In FT-IR spectra, the vanadyl peaks are co-existed with the L1 structure, which confirmed the complex formation of the L1 with vanadium. Similarly, the binding energy of V(IV) was identified at 516.2 eV for V2p3/2 in XPS spectra. The new strategy for VOSO4 recovery was established through solvent extraction and acid leaching. After recovery process, the absence of vanadium peak in the XPS confirmed the complete removal of V(IV) from the complex. The recovered VOSO4 solution used as an electrolyte in vanadium redox flow battery (VRFB) systems, where the unit cell performance is comparable with the conventional electrolyte solution. The advantage of study is reuse of VOSO4 as a resource for energy storage applications.

Naturally available diatomite and their surface modification for the removal of hazardous dye and metal ions: A review.

The presence of toxic pollutants such as dyes and metal ions at higher concentrations in water is very harmful to the environment. Removal of these pollutants using diatomaceous earth or diatomite (DE) and surface-modified DE has been extensively explored due to their excellent physio-chemical properties and low cost. Therefore, naturally available DE being inexpensive, their surface modified adsorbents could be one of the potential candidates for the wastewater treatment in the future. In this context, the current review has been summarized for the removal of both pollutants i.e., dyes and metal ions by surface-modified DE using the facile adsorption process. In addition, this review is prominently focused on the various modification process of DE, their cost-effectiveness; the physio-chemical characteristics and their maximum adsorption capacity. Further, real-time scenarios of reported adsorbents were tabulated based on the cost of the process along with the adsorption capacity of these adsorbents.