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Activated carbon (AC) based adsorbents derived from waste sludge were utilized to remediate mixed contaminants in wastewater as an integrated waste-to-resource approach promoting a paradigm shift in management of refuse sludge and wastewater. This review specifically focuses on the remediation of constituents of landfill leachate by sludge-based activated carbon (SBAC). The adsorption effectiveness of SBAC for the exclusion of leachate characters including heavy metals, phenols, dyes, phosphates, and phosphorus were explored with regard to modifiers such as pH, temperature, properties of the adsorbent including functional groups, initial doses of absorbent and adsorbate, and duration of exposure to note the impact of each parameter on the efficiency of adsorption of the sludge adsorbent. Through the works of various researchers, it was noted that the properties of the adsorbent, pH and temperature impact the working of SBACs. The pH of the adsorbent by influencing the functional groups. Temperature was expected to have a paramount effect on the adsorption efficiency of the SBACs. The importance of the regeneration and recycling of the adsorbents as well as their leachability is highlighted. Sludge based activated carbon is recommended as a timely, resource-efficient, and sustainable approach for the remediation of wastewater.
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Carvão Vegetal , Esgotos , Poluentes Químicos da Água , Poluentes Químicos da Água/química , Poluentes Químicos da Água/análise , Esgotos/química , Carvão Vegetal/química , Adsorção , Águas Residuárias/química , Eliminação de Resíduos Líquidos/métodos , Concentração de Íons de Hidrogênio , Temperatura , Purificação da Água/métodosRESUMO
Dearomatization through photocatalytic oxidation is a swiftly rising phenolic compounds removal technology that works at trifling operations requirements with a special emphasis on the generation of nontoxic products. The study aims to develop a LaVO4/MCM-48 nanocomposite that was prepared via a hydrothermally approach assisting the employment of an MCM-48 matrix, which was then utilized for phenol degradation processes. Various techniques including UV-Vis DRS, FTIR, PL, Raman, TEM, and BET analyses are employed to characterize the developed photocatalyst. The developed photocatalyst presented remarkable characteristics, especially increased light photon utilization, and reduced recombination rate leading to enhanced visible-light-driven photodegradation performance owing to the improved specific surface area, specific porosities, and <2 eV narrow energy bandgap. The LaVO4/MCM-48 nanocomposite was experienced on aqueous phenol solution having 20 mg/L concentration under visible-light exposure, demonstrating exceptional performance in photodegradation up to 99.28%, comparatively higher than pure LaVO4. The conducted kinetic measurements revealed good accordance with pseudo first-order. A possible reaction mechanism for photocatalytic degradation was also predicted. The as-synthesized LaVO4/MCM-48 nanocomposite presented excellent stability and recyclability.
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Nanocompostos , Fenol , Águas Residuárias , Luz , FenóisRESUMO
Researchers have focused on efficient techniques for degrading hazardous organic pollutants due to their negative impacts on ecological systems, necessitating immediate remediation. Specifically, TiO2-based photocatalysts, a wide-bandgap semiconductor material, have been extensively studied for their application in environmental remediation. However, the extensive band gap energy and speedy reattachment of electron (e-) and hole (h+) pairs in bare TiO2 are considered major disadvantages for photocatalysis. This review extensively focuses on the combination of semiconducting photocatalysts for commercial outcomes to develop efficient heterojunctions with high photocatalytic activity by minimizing the e-/h+ recombination rate. The improved activity of these heterojunctions is due to their greater surface area, rich active sites, narrow band gap, and high light-harvesting tendency. In this context, strategies for increasing visible light activity, including doping with metals and non-metals, surface modifications, morphology control, composite formation, heterojunction formation, bandgap engineering, surface plasmon resonance, and optimizing reaction conditions are discussed. Furthermore, this review critically assesses the latest developments in TiO2 photocatalysts for the efficient decomposition of various organic contaminants from wastewater, such as pharmaceutical waste, dyes, pesticides, aromatic hydrocarbons, and halo compounds. This review implies that doping is an effective, economical, and simple process for TiO2 nanostructures and that a heterogeneous photocatalytic mechanism is an eco-friendly substitute for the removal of various pollutants. This review provides valuable insights for researchers involved in the development of efficient photocatalysts for environmental remediation.
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Poluentes Ambientais , Recuperação e Remediação Ambiental , Titânio/química , Catálise , LuzRESUMO
Novel Ag3VO4/KIT-6 nanocomposite photocatalyst has been successfully fabricated by a newly-designed simple hard-template induction process, in which the particles of Ag3VO4 were grown on the KIT-6 surface and inside the porous framework of the silica matrix. The developed porous framework nanocomposite was characterized by several techniques including N2-Physiosorption analysis. The obtained nanocomposite revealed a high surface area (273.86 m2/g) along with the possession of monoclinic Ag3VO4, which is highly responsive to visible light (with distinct intensity at about 700 nm). The UV-Vis DRS reveals that the Ag3VO4/KIT-6 photocatalyst bears a bandgap of 2.29 eV which confirms that the material has a good visible light response. The synthesized nanocomposite was tested for its superior physicochemical properties by evaluating its degradation efficiency for Congo Red (CR). The novel composite exhibited superior degradation capability of CR, reaching up to 96.49%, which was around three times the pure Ag3VO4. The detailed kinetic study revealed that the as-prepared material followed a pseudo first order kinetic model for the CR degradation. The study includes a comprehensive parametric study for the formulation of the optimized reaction conditions for photocatalytic reactions. The commercial applicability of the composite material was investigated by a regeneration and recyclability test, which revealed extraordinary results. Furthermore, the possible degradation pathway for CR was also proposed.
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The case of a 60 year old male patient, diagnosed with rheumatoid arthritis presenting with recurrent massive pericardial effusion, and unresponsive to treatment of rheumatoid arthritis is documented. Pericardial biopsy proved Tuberculous pericarditis with positive fluid culture for Mycobacterium Tuberculosis. Anti-tuberculous treatment was started along with corticosteroids. Follow up after three months showed no evidence of pericardial effusion.
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Artrite Reumatoide/complicações , Mycobacterium tuberculosis/isolamento & purificação , Derrame Pericárdico/etiologia , Pericardite Tuberculosa/diagnóstico , Corticosteroides/uso terapêutico , Artrite Reumatoide/tratamento farmacológico , Biópsia , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Derrame Pericárdico/tratamento farmacológico , Derrame Pericárdico/patologia , Pericardite Tuberculosa/tratamento farmacológico , Pericardite Tuberculosa/microbiologia , Recidiva , Resultado do TratamentoRESUMO
Polluted water resources, particularly those polluted with industrial effluents' dyes, are carcinogenic and hence pose a severe threat to sustainable and longstanding worldwide development. Meanwhile, adsorption is a promising process for polluted/wastewater treatment. In particular, activated carbon (AC) is popular among various wastewater treatment adsorbents, especially in the organic contaminants' remediation in wastewater. Hence, the AC's synthesis from degradable and non-degradable resources, the carbon activation involved in the AC synthesis, and the AC's modification to cutting-edge and effective materials have been modern-research targets in recent years. Likewise, the main research focuses worldwide have been the salient AC characteristics, such as its surface chemistry, porosity, and enhanced surface area. Notably, various modified-AC synthesis methods have been employed to enhance the AC's potential for improved contaminants-removal. Hence, we critically analyze the different modified ACs (with enhanced (surface) functional groups and textural properties) of their capacity to remove different-natured anionic dyes in wastewater. We also discuss the corresponding AC modification techniques, the factors affecting the AC properties, and the modifying agents' influence on the AC's morphological/adsorptive properties. Finally, the AC research of future interest has been proposed by identifying the current AC research gaps, especially related to the AC's application in wastewater treatment.
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Águas Residuárias , Poluentes Químicos da Água , Adsorção , Carvão Vegetal/química , Corantes , Águas Residuárias/química , Poluentes Químicos da Água/análiseRESUMO
BACKGROUND: A combination of biologically active ligand and metal in one molecule may increase the activity and reduce the toxicity. OBJECTIVES: In this study, the synthesis and characterization of platinum(IV) complexes with bioactive hydrazide ligands are discussed. METHOD: Elemental analysis, conductivity measurements, and spectroscopic studies were used to elucidate the structure of complexes. RESULTS: Our study suggests that hydrazide ligands coordinate with Pt(IV) in a bidentate fashion. The platinum(IV) complexes have octahedral geometry with a metal to ligand ratio of 1:2. Hydrazide ligands were coordinated with central metal platinum(IV) by oxygen of carbonyl group and nitrogen of primary amine. Synthesized complexes exhibited variable DPPH radical scavenging and lipoxygenase inhibition activity. Furthermore, it is also found that Pt(IV)-hydrazide complexes are more potent superoxide and nitric oxide radical scavengers than their uncoordinated hydrazide ligands, while in the case of lipoxygenase enzyme inhibition, some of the free hydrazide ligands are more active than their respective Pt(IV) complexes. In silico docking technique explores molecular interactions of synthesized ligands in the active site of the lipoxygenase enzyme. Predicted docking energies are in good agreement with experimental data suggesting that in silico studies might be useful for the discovery of therapeutic candidates. CONCLUSION: Structure-function relationship demonstrates that the radical scavenging and enzyme inhibition activities of the Pt(IV) compounds are affected by the nature of the ligand, position of substituent, electronic and steric effects. However, electronic factors seem to play a more important role than other factors.
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Antioxidantes , Complexos de Coordenação , Antioxidantes/farmacologia , Inibidores Enzimáticos , Hidrazinas , Ligantes , Inibidores de Lipoxigenase/farmacologia , Estrutura Molecular , PlatinaRESUMO
The world's water supplies have been contaminated due to large effluents containing toxic pollutants such as dyes, heavy metals, surfactants, personal care products, pesticides, and pharmaceuticals from agricultural, industrial, and municipal resources into water streams. Water contamination and its treatment have emerged out as an escalating challenge globally. Extraordinary efforts have been made to overcome the challenges of wastewater treatment in recent years. Various techniques such as chemical methods like Fenton oxidation and electrochemical oxidation, physical procedures like adsorption and membrane filtration, and several biological techniques have been recognized for the treatment of wastewater. This review communicates insights into recent research developments in different treatment techniques and their applications to eradicate various water contaminants. Research gaps have also been identified regarding multiple strategies for understanding key aspects that are important to pilot-scale or large-scale systems. Based on this review, it can be determined that adsorption is a simple, sustainable, cost-effective, and environmental-friendly technique for wastewater treatment, among all other existing technologies. However, there is a need for further research and development, optimization, and practical implementation of the integrated process for a wide range of applications.
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Metais Pesados , Poluentes Químicos da Água , Purificação da Água , Adsorção , Eliminação de Resíduos Líquidos , Águas Residuárias/análise , Poluentes Químicos da Água/análiseRESUMO
In this study, titania/silica nanocomposite and mesoporous TiO2 (m-TiO2) photocatalysts are developed by KIT-6 template via a sol-gel approach. The synthesized photocatalysts are characterized by XRD, EDX, SEM, Raman, PL, and UV-vis DRS analysis techniques. The as-synthesized series revealed a high surface area, smaller size, a greater number of accessible active sites, and enhanced light-harvesting capability. The m-TiO2 photocatalysts' charge recombination capability was curiously inferior to the rest of as-synthesized TiO2/KIT-6 nanocomposite materials. The band-gap of as-synthesized materials were suitable for their activity in UV light irradiations. It was pragmatic that the photocatalytic degradation efficiency of m-TiO2 photocatalysts was superior as compared to that of commercial TiO2 photocatalyst under UV light irradiations, owing to the synergistic outcome of the anatase phase and a greater number of accessible active-sites availability as a result of high surface area. Moreover, the m-TiO2 was critically evaluated by investigating various parameters affecting the photocatalytic degradation reaction of MB including the effect of irradiation time, pH, catalyst dosage, and dye concentration. The m-TiO2, 45wt% composite material and commercial-TiO2 exhibited 99.27, 91.20, and 84.67% degradation of methyl blue in 50 min, respectively. Finally, the m-TiO2 exhibited excellent recyclability with negligible loss of activity performance.
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Benzenossulfonatos , Titânio , CatáliseRESUMO
Mineral stress is one of the major abiotic stresses faced by crop plants. The present study was undertaken to investigate the impact of mineral stress (iron (Fe) and phosphorus (P)) on various morphological and biochemical responses of the shoot and root tissues and root architecture of common bean (Phaseolus vulgaris L.). This study also leads us to the identification of P stress responsive proteins. The study was conducted under in vitro conditions, in which seeds of Shalimar French Bean-1 (SFB-1) variety were cultured on four different MGRL medium (control (P1Fe1), iron deficient (P1Fe0), phosphorus deficient (P0Fe1), and phosphorus and iron deficient (P0Fe0)). Chlorophyll content of leaves, Fe/P content of root tissues, total sugars, proline, length, and weight of shoot and root tissues were assessed and compared within and between the treatments. The analyzed data revealed significant difference between control and other three treatments. Chlorophyll content of shoots was found significantly decreased under mineral stress treatments P0Fe1, P1Fe0, and P0Fe0 than control. Length and weight of shoot and root were also observed significantly decreased under P0Fe1, P1Fe0, and P0Fe0 as compared to control. Total sugar was significantly higher in P0Fe1 of roots in comparison to control. Proline content was significantly higher in both tissues of shoots and roots of plants grown under P1Fe0, P0Fe1, and P0Fe0 than control condition. Furthermore, we unexpectedly observed the recovery of roots (mainly primary roots) under P0Fe0 as compared to P1Fe0 and P0Fe1. Interestingly higher concentration of Fe was also observed in P0Fe1 compared to other treatments and also higher concentration of P was observed in P1Fe1. These findings suggested that there is a crosstalk between Fe and P and also revealed that there is a disruption in the ability of PR (primary root) to sense local P deficiency in the absence of Fe. Furthermore, proteomics analysis (SDS-PAGE followed by MALDI MS) helped in identification of defensive proteins in P stress condition compared to control.
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Regulação da Expressão Gênica de Plantas , Ferro/metabolismo , Phaseolus/crescimento & desenvolvimento , Fósforo/metabolismo , Raízes de Plantas/crescimento & desenvolvimento , Proteômica , Ferro/farmacologia , Fósforo/farmacologiaRESUMO
The organosulfur compounds present in liquid fuels are hazardous for health, asset, and the environment. The photocatalytic desulfurization technique works at ordinary conditions and removes the requirement of hydrogen, as it is an expensive gas, highly explosive, with a broader flammability range and is declared the most hazardous gas within a petroleum refinery, with respect to flammability. The projected work is based on the synthesis of V2O5 microspheres for photocatalytic oxidation for the straight-run diesel (SRD) and diesel oil blend (DOB). The physicochemical properties of V2O5 microspheres were examined by FT-IR, Raman, UV-vis DRS, SEM, and Photoluminescence evaluations. The as-synthesized photocatalyst presented a trivial unit size, a narrow bandgap, appropriate light-capturing capability, and sufficient active sites. The desulfurization study discovered that the anticipated technique is substantial in desulfurizing DOB up to 37% in 180 min using methanol as an interfacing agent. Furthermore, the outcome of employing a range of polar interfacing solvents was examined, and the 2-ethoxyethanol elevated the desulfurization degree up to 51.3%. However, the anticipated technology is constrained for its application in sulfur removal from SRD. Additionally, the mechanism for a photocatalytic reaction was seen in strong agreement with pseudo-first-order kinetics. The investigated photocatalyst exhibited a compromised recyclability and regeneration tendency.
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Mixed matrix membranes (MMMs) were fabricated by the hydrothermal synthesis of ordered mesoporous KIT-6 type silica and incorporating in polyimide (P84). KIT-6 and MMMs were characterized to evaluate morphology, thermal stability, surface area, pore volume, and other characteristics. SEM images of synthesized MMMs and permeation data of CO2 suggested homogenous dispersion of mesoporous fillers and their adherence to the polymer matrix. The addition of KIT-6 to polymer matrix improved the permeability of CO2 due to the increase in diffusivity through porous particles. The permeability was 3.2 times higher at 30% loading of filler. However, selectivity showed a slight decrease with the increase in filler loadings. The comparison of gas permeation results of KIT-6 with the well-known MCM-41 revealed that KIT-6 based MMMs showed 14% higher permeability than that of MMMs composed of mesoporous MCM-41. The practical commercial viability of synthesized membranes was examined under different operating temperatures and mixed gas feeds. Mesoporous KIT-6 silica is an attractive additive for gas permeability enhancement without compromising the selectivity of MMMs. Graphical abstract.
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Dióxido de Carbono , Polímeros , Membranas Artificiais , PermeabilidadeRESUMO
BACKGROUND: Antioxidant, anti-inflammatory, antiviral and antitumoral activities among others are essential characteristics in the development of novel therapeutic compounds. Acid hydrazides can form complexation with certain metal ions that positively enhance these biological characteristics. OBJECTIVE: Five new complexes of uranium with hydrazide ligands were synthesized at room temperature. METHODS: The characterization was done by spectroscopic methods (ESI-Mass, IR, 1H-NMR, 13CNMR), CHN analysis and conductivity measurements. Metal complexes along with their respective ligands were further screened for their antioxidant (DPPH, superoxide and nitric oxide free radicals) properties and enzyme inhibition (α-glucosidase) activities. RESULTS: Elemental and spectral data indicate octahedral geometry around uranyl (UO2 2+) species. Magnetic moments indicate the diamagnetic nature of uranyl(VI) ion in the complex in solid state. IC50 values showed potential antioxidant behavior of uranyl complexes demonstrating interesting structure-activity relationships. In general, hydrazide ligands were not active against superoxide and nitric oxide radicals while varying degree of results were observed against DPPH radical whereas all uranyl-complexes showed promising radical scavenging activities against all of them. Promising inhibitory potential was displayed by UO2 +2 hydrazide complexes against α- glucosidases whereas free hydrazide ligands were inactive. CONCLUSION: Structure function relationship demonstrates that the nature of ligand, position of substituent, electronic and steric effects are significant factors affecting the radical scavenging and enzyme inhibition activities of the compounds.
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Complexos de Coordenação/química , Complexos de Coordenação/farmacologia , Hidrazinas/química , Urânio/química , alfa-Glucosidases/metabolismo , Compostos de Bifenilo/química , Sequestradores de Radicais Livres/química , Sequestradores de Radicais Livres/farmacologia , Inibidores de Glicosídeo Hidrolases/química , Inibidores de Glicosídeo Hidrolases/farmacologia , Concentração Inibidora 50 , Óxido Nítrico/química , Picratos/químicaRESUMO
Photocatalytic H2 production is a promising strategy toward green energy and alternative to carbon-based fuels which are the root cause of global warming and pollution. In this study, carbon nanotubes (CNTs) incorporated Z-scheme assembly of AgBr/TiO2 was developed for photocatalytic H2 production under visible light irradiations. Synthesized photocatalysts were characterized through transmission electron microscope (TEM), X-ray photoelectron spectra (XPS), X-ray diffractometer (XRD), Fourier transform infrared (FTIR), photoluminescence spectra (PL), Brunauer Emmet-Teller(BET), and UV-vis spectroscopy analysis techniques. The composite photocatalysts exhibited a H2 production of 477 ppm which was three-folds higher than that produced by TiO2. The good performance was attributed to the strong interaction of three components and the reduced charge recombination, which was 89 and 56.3 times lower than the TiO2 and AgBr/TiO2. Furthermore, the role of surface acidic and basic groups was assessed and the photocatalytic results demonstrated the importance of surface functional groups. In addition, the composites exhibited stability and reusability for five consecutive cycles of reaction. Thus, improved performance of the photocatalyst was credited to the CNTs as an electron mediator, surface functional groups, higher surface area, enhanced charge separation and extended visible light absorption edge. This work provides new development of Z-scheme photocatalysts for sustainable H2 production.
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In this work, new nanoporous silica (Korea Advanced Institute of Science and Technology-6 (KIT-6)-dried or KIT-6-calcined) incorporated with isolated Ti materials with different Si/Ti ratios (Si/Ti = 200, 100, and 50) has been synthesized and investigated to establish photocatalytic reduction of CO2 in the presence of H2O vapors. The properties of the materials have been characterized through N2 adsorption/desorption, UV-vis, TEM, FT-IR, and XPS analysis techniques. The intermediate amount of the isolated Ti (Si/Ti = 100) has resulted to be more uniformly distributed on the surface and within the three-dimensional pore structure of the KIT-6 material, without its structure collapsing, than the other two ratios (Si/Ti = 200 and 50). However, titania agglomerates have been observed to have formed due to the increased Ti content (Si/Ti = 50). The Ti-KIT-6 (calcined) materials in the reaction showed higher activity than the Ti-KIT-6 (dried) materials, which produced CH4, H2, CO, and CH3OH (vapors) as fuel products. The Ti-KIT-6 (Si/Ti = 100) material also showed more OH groups, which are useful to obtain a higher production rate of the products, particularly methane, which was even higher than the rate of the best commercial TiO2 (Aeroxide P25, Evonik Industries AG, Essen, Germany) photocatalyst.