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The sustainable catalytic efficacy of transition metal oxides (TMO) and rare earth element-based oxides positions them as pivotal materials for effectively treating contaminated wastewater. This study successfully synthesized a series of Ce@MnO2 photocatalysts using a straightforward hydrothermal method. These photocatalysts were thoroughly characterized for their optical properties, structural morphology, and phase purity. Among the synthesized materials, the Ce@MnO2 (40:60) exhibited the highest photocatalytic activity for the degradation of Acebutolol (ACB), achieving a remarkable degradation efficiency of 92.71% within 90 min under visible light irradiation. This superior performance is attributed to the increased presence of active species and the efficient separation of photogenerated carriers. Additionally, the photocatalytic reaction mechanism was elucidated, highlighting the catalyst's surface charge properties which significantly enhanced performance in a solution with pH 8. The outstanding photo-response in the visible spectrum renders this method not only cost-effective but also environmentally benign, presenting a promising approach for large-scale water purification.
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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.
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Nanosferas , Poluentes Químicos da Água , Carbono/química , Corantes/química , Areca , Adsorção , Porosidade , Nozes/química , Análise Custo-Benefício , Poluentes Químicos da Água/análise , Cinética , Azul de Metileno/química , Concentração de Íons de HidrogênioRESUMO
Poly(3,4-ethylenedioxythiophene) (PEDOT) and PEDOT-functionalized carbon nanoparticles (f-CNPs) were synthesized by in situ chemical oxidative polymerization and pyrolysis methods. f-CNP-PEDOT nanocomposites were prepared by varying the concentration of PEDOT from 1 to 20% by weight (i.e., 1, 2.5, 5, 10, and 20 wt%). Several characterization techniques, such as field-emission scanning electron microscopy (FESEM), attenuated total reflectance-Fourier transform infrared (ATR-FTIR), X-ray diffraction (XRD), N2 Brunauer-Emmett-Teller (BET) and Barrett-Joyner-Halenda (BJH) analyses, as well as cyclic voltammetry (CV), galvanostatic charge discharge (GCD), and electrochemical impedance spectroscopy (EIS), were applied to investigate the morphology, the crystalline structure, the N2 adsorption/desorption capability, as well as the electrochemical properties of these new synthesized nanocomposite materials. FESEM analysis showed that these nanocomposites have defined porous structures, and BET surface area analysis showed that the standalone f-CNP exhibited the largest surface area of 801.6 m2/g, whereas the f-CNP-PEDOT with 20 wt% exhibited the smallest surface area of 116 m2/g. The BJH method showed that the nanocomposites were predominantly mesoporous. CV, GCD, and EIS measurements showed that f-CNP functionalized with 5 wt% PEDOT had a higher capacitive performance compared to the individual f-CNPs and PEDOT constituents, exhibiting an extraordinary specific capacitance of 258.7 F/g, at a current density of 0.25 A/g, due to the combined advantage of enhanced electrochemical activity induced by PEDOT doping, and highly developed porosity of f-CNPs. Symmetric aqueous supercapacitor devices were fabricated using the optimized f-CNP-PEDOT doped with 5 wt% of PEDOT as active material, exhibiting a high capacitance of 96.7 F/g at 1.4 V, holding practically their full charge, after 10,000 charge-discharge cycles at 2 A/g, thus providing the highest electrical electrodes performance. Hereafter, this work paves the way for the potential use of f-CNP-PEDOT nanocomposites in the development of high-energy-density supercapacitors.
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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.
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Separação Celular , Células Neoplásicas Circulantes , Humanos , Células Neoplásicas Circulantes/patologia , Células MCF-7 , Separação Celular/métodos , Dispositivos Lab-On-A-Chip , Técnicas Analíticas Microfluídicas , Nanopartículas de Magnetita/química , Neoplasias da Mama/patologia , FemininoRESUMO
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.
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Arsênio , Polímeros , Polímeros/química , Membranas Artificiais , Água , ÍonsRESUMO
In this study, novel V2O5-decorated garlic peel biochar (VO/GPB) nanocomposites are prepared via the facile hydrothermal technique. As-synthesized VO/GPB is characterized by various spectroscopic and analytical techniques. The surface morphology of the as-prepared samples was predicted by SEM analysis, which shows that the block-like V2O5 was uniformly decorated on the stone-like GPB surface. The elemental mapping analysis confirms the VO/GPB composite is composed of the following elements: C, O, Na, Mg, Si, P, K, and V, without any other impurities. The photocatalytic activity of the VO/GPB nanocomposite was examined by the degradation of methyl orange (MO) under the irradiation of visible light; 84% degradation efficiency was achieved within 30 min. The reactive oxidative species (ROS) study reveals that hydroxyl and superoxide radicals play an essential role in MO degradation. Moreover, the antioxidant action of the VO/GPB nanocomposite was also investigated. From the results, the VO/GPB composite has higher antioxidant activity compared to ascorbic acid; the scavenging effect increased with increasing concentrations of VO/GPB composite until it reached 40 mg/L, where the scavenging effect was the highest at 93.86%. This study will afford innovative insights into other photocatalytic nanomaterials with effective applications in the field of photocatalytic studies with environmental compensation.
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Selective laser sintering (SLS) is an additive manufacturing process that has shown promise in the production of medical devices, including hip cups, knee trays, dental crowns, and hearing aids. SLS-based 3D-printed dosage forms have the potential to revolutionise the production of personalised drugs. The ability to manipulate the porosity of printed materials is a particularly exciting aspect of SLS. Porous tablet formulations produced by SLS can disintegrate orally within seconds, which is challenging to achieve with traditional methods. SLS also enables the creation of amorphous solid dispersions in a single step, rather than the multi-step process required with conventional methods. This review provides an overview of 3D printing, describes the operating mechanism and necessary materials for SLS, and highlights recent advances in SLS for biomedical and pharmaceutical applications. Furthermore, an in-depth comparison and contrast of various 3D printing technologies for their effectiveness in tissue engineering applications is also presented in this review.
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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 â¦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.
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Alho , Nanosferas , Carbono , Concentração de Íons de Hidrogênio , Cinética , Corantes de Rosanilina , Água/químicaRESUMO
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.
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Dióxido de Silício , Poluentes Químicos da Água , Adsorção , Compostos Azo , Hidróxidos , Cinética , Poluentes Químicos da Água/análiseRESUMO
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.
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Cério , Estruturas Metalorgânicas , Poluentes Químicos da Água , Purificação da Água , Adsorção , Cério/toxicidade , Poluentes Químicos da Água/análiseRESUMO
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.
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Diatomaceous earth or diatom (DE) are naturally available and low cost micro particles with distinct porous structure were used as an adsorbent for the removal of a hazardous dye, Eriochrome Black T (EBT). The surface modification of these DE were performed by sol-gel and hydrothermal methods to obtain a series of adsorbents such as diatom-ceria (DC), diatom-silica xerogel (DX), and diatom-silica xerogel-ceria (DXC). A cauliflower like morphology structure of ceria was observed on DE and DX. The adsorption performance of EBT was conducted by varying various parameters such as pH, adsorbent dosage, initial concentration, contact time and ionic strength. The materials DE, DC, DX and DXC showed the EBT removal efficiencies of 52, 77, 20, and 93%, respectively. The maximum adsorption capacity (qm) of DE, DC, DX and DXC was found to be 13.83, 23.64, 0.2 and 47.02â¯mgg-1 for the adsorption of EBT, respectively. The selectivity of EBT towards DXC was evaluated by treating a mixture of anionic dyes. The dye removal experiments was performed in presence of inorganic salts, however the presence of these salts did not affect the removal efficiency of DXC. Furthermore, the reusability of DXC was studied by recycling it up to 5 times and even at 5th cycle a removal efficiency of â¼66.8% was found. Thus, these studies demonstrate that the DXC material could be a promising candidate for the removal of EBT via adsorption for real time application in water treatment.