Contact Time Research Articles

Engineered hybrid iron‐cobalt metal oxide nanoparticles for effective adsorption of malachite green dye

AbstractBACKGROUNDHybrid iron and cobalt metal oxide nanoparticles are well known; however, are not optimized in terms of size and stability. We engineered these hybrid nanoparticles using the co‐precipitation method and characterized them by various techniques, which are then used for the effective adsorption and removal of malachite green (MG) dye.RESULTSThe ideal conditions for synthesis are determined to be 50:50 ratio of Fe2O3 and CoO, pH of 11, temperature range of 40 °C–60 °C, and reactant addition time of 20 min. These hybrid nanoadsorbents effectively eliminated MG dye from aqueous solutions. Factors such as initial MG dye concentration, pH of the medium, contact time, temperature, and nanoadsorbent dose were optimized for the MG removal to achieve a maximum removal efficiency of 96.9%. Non‐linear fitting of data indicates that both Langmuir and Freundlich models provided the best fit, suggesting the presence of both monolayer and multilayer adsorption of MG on hybrid nanoparticles. The kinetics of MG dye removal are better controlled by the intraparticle diffusion (IPD) phenomenon. The adsorption of MG onto the hybrid nanoparticles was confirmed to be endothermic, with negative ΔG and positive ΔH values. The optimized synthetic conditions also positively impacted the hybrid nanoparticles which enhanced the adsorption and exhibited ferromagnetic behavior as compared to the superparamagnetic behavior reported in the literature, making them significantly important for dye removal applications.CONCLUSIONThese findings demonstrate the potential of optimized hybrid nanoparticles as effective nanoadsorbents for dye removal applications, with implications for further applications in photocatalysis and sensing. © 2024 Society of Chemical Industry (SCI).

Effective removal of textile dye via synergy of adsorption and photocatalysis over ZnS nanoparticles: Synthesis, modeling, and mechanism

In this work, we prepared sulfur-zinc nanoparticles (ZnS-TGA) functionalized with thioglycolic acid by a hydrothermal method and tested their photodegradation ability by solar irradiation. ZnS-TGA were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), high-resolution transmission electron microscope (HR-TEM), UV–Vis spectrophotometer and photoluminescence spectroscopy. In the characterization of these nanoparticles, thioglycolic acid proved to be a strong capping ligand, with a specific surface area of 36.82 m2/g and an average size of 7.15 nm. To test the photocatalytic degradability of the product, methylene blue (MB) was used as a model pollutant. Various operational variables were investigated, including pH, amount of nanoparticles, dye concentration, contact time and temperature. The equilibrium adsorption tests, and the statistical physical calculations allowed the analysis of the energetic and steric variables of the adsorption of MB dye molecules on the surface of these nanoparticles. The equilibrium data were well fitted with Langmuir-Freundlich (L-F) and the adsorption kinetics with pseudo-first order. The maximum adsorption capacity of the MB dye removal process was 30.92 mg g−1 at pH 7 and 298 K, and this process was spontaneous and exothermic. The dye molecules and the surface of the nanoparticles exhibited physical interactions with adsorption energies of 23.31–25.92 kJ/mol. The photocatalytic activity of these nanoparticles resulted in a dye degradation efficiency of 91.1 % in 180 min. The photocatalytic efficiency remained almost unchanged after five consecutive degradation cycles, resulting in a methylene blue degradation of 85 %. According to these results, these environmentally friendly nanoparticles have the potential to purify industrial and urban liquids contaminated with harmful organic compounds such as dye molecules.

Nano‐Enhanced Water Purification: Uncovering the Dye Adsorption Efficiency of Ni‐Zn‐S@Cyclodextrine Nanomaterial

AbstractThis research investigates the synthesis of a hybrid nanomaterial, denoted as Ni‐Zn−S@Cyclodextrine, through a cost‐effective and easy co‐precipitation method. The resulting nanomaterial has been thoroughly characterized and applied for the adsorptive removal of Crystal violet and Congo red dyes from their solutions. The study delves into the thermodynamics and kinetics of the sorption process, as well as helps to propose adsorption mechanism for both the dyes onto the Ni‐Zn−S@Cyclodextrine surface. A comprehensive analysis, encompassing techniques, such as XRD, FTIR, SEM‐EDX, TEM, TGA, Zeta potential, and XPS, have been conducted to explore the structural and morphological attributes of the prepared nanomaterial. Furthermore, key sorption parameters, including adsorbent's dosage, temperature, contact time, and solution pH, have been systematically optimized to achieve maximum efficiency. The TEM images of prepared nanomaterial indicated the particle size ranging between 60–80 nm. Moreover, it exhibited a strong affinity for both the dyes, with a maximum adsorption capacity of 138.20 mgg−1 for Congo red and 129.95 mgg−1 for Crystal violet dyes at 303 K. The thermodynamics of the adsorption process indicated an endothermic and spontaneous nature. Isotherm studies revealed that the data best aligned with the Freundlich isotherm, while the kinetics of the reaction adhered to a pseudo‐second order within the investigated temperature range.

Management of medically unexplained symptoms in children and young people: a secondary analysis of a 10-year audit of referrals to a Paediatric Psychology Service

This study evaluated service use of children and young people with medically unexplained symptoms (MUS) referred to a Paediatric Psychology Service between 2008 and 2017. Univariate analyses of activity data...

Valorizing Moroccan crab shells to purify water from Orange G dye: Exploring equilibrium, kinetics, and thermodynamics

A successful approach has been taken to develop a biomaterial derived from fish waste, using Moroccan fish processing by-products from crab shells. Moroccan crab (Portunus pelagicus) shell-derived biomaterial has been developed for wastewater treatment, using marine crustacean waste and addressing the challenges of solid fish waste management. The crab shell powder (CSP) was calcined at 800 °C for three hours and characterized using SEM, EDS, FTIR, and XRD, revealing a predominantly crystalline structure. The CSP's effectiveness as a biosorbent for the removal of the anionic dye Orange G (OG) was assessed under various conditions, including pH, biosorbent mass, temperature, and contact time. Optimal conditions achieved a 98.84 % dye removal rate within 60 min at an adsorbent dose of 0.09 g. The adsorption process adhered to the pseudo-second-order kinetic model and the Freundlich isotherm, indicating a spontaneous, endothermic surface reaction involving multilayer physisorption. The biosorption mechanism is thought to include electrostatic attractions, n-π stacking interactions, hydrogen bonding, and Yoshida hydrogen bonds. The study suggests that CSP is an efficient, eco-friendly adsorbent for industrial wastewater treatment, offering a promising solution for the valorization of fish waste by-products.

Corn Husk‐Derived Carbon Fused with Iron Oxide as Adsorbent for Cationic Dyes

AbstractThe development of nanomaterials for dye degradation has garnered significant interest due to their efficiency, environmental benefits, and cost‐effectiveness. In this study, a nanocomposite adsorbent composed of α‐Fe2O3 coupled with carbon derived from eco‐friendly corn husk has been developed. This material effectively captured cationic dyes, Methylene Blue (MB) and Malachite Green (MG), from aqueous solutions, including industrial dye effluent from local industry. The synthesized nanocomposite demonstrated rapid removal of MB and MG from the solution without the need for additional oxidizing or reducing agents. The adsorption conditions by varying parameters such as adsorbent dose, contact time, solution pH, initial dye concentration, and temperature have been optimized. Adsorption isothermal studies indicated that the Langmuir isotherm model best explained the adsorption process. Kinetic studies revealed that the adsorption process follows a pseudo‐first‐order model for MB, while the intraparticle diffusion model is more appropriate for MG. Moreover, the nanocomposite exhibited excellent reusability and regenerability for dye adsorption. Our study showcases the effectiveness of the synthesized nanocomposite adsorbent, comprising α‐Fe2O3 integrated with carbon derived from eco‐friendly corn husk using a simple and sustainable methodology, in efficiently removing cationic dyes from textile wastewater. This approach offers a promising solution for environmental remediation.

Photocurable Foam for Three-Dimensional-Printed Porous Structures.

In this research, a foam three-dimensional (3D) printing method using digital light processing (DLP) technology was developed to fabricate 3D-printed porous structures. To address the challenges in preparing DLP precursor foam fluid, we designed a specialized foaming device. This device enables the precursor solution to be blended with air, resulting in a stable foam precursor with an adjustable air/liquid fraction and suitable fluidity, crucially enhancing the gas-liquid contact time for the printing process. By manipulation of fluid flow rates, cycle counts, and gas/liquid ratios, one can easily prepare uniform foams with precise control over the pore size and porosity. To avoid significant volume reduction during ultraviolet (UV) curing, nanoparticle fillers were introduced into the network to prevent collapse of the foam structure. Furthermore, the inclusion of an UV absorber enhanced the quality of the printing process by addressing the limitations associated with particle scattering and reflection. The DLP process can readily fabricate intricate structures, featuring a planar resolution below 30 μm and a printing accuracy of less than 1%. Several examples were also demonstrated to highlight the advantages of this technology and its ability to directly print custom foam structures, thereby saving time and material resources.

Green synthesis of zinc oxide nanoparticles for the removal of phenol from textile wastewater

This study investigated the use of zinc oxide nanoparticles (ZnO NPs) as an adsorbent for removing total phenols from textile wastewater. The ZnO NPs were synthesized by reducing Zn(NO3)2⋅6H2O using an extract from Neem leaves (Azadirachta indica). Characterization of the adsorbent was performed using Fourier Transform Infrared (FTIR) spectroscopy to identify functional group modifications, high-resolution scanning electron microscopy (HRSEM) for structural orientation, energy dispersive spectroscopy (EDS) for elemental analysis, and X-Ray diffraction analysis (XRD) for crystallinity, revealing particle crystallinity around 200 nm. Adsorption experiments were conducted over contact times of 20–60 min, with adsorbent loadings between 0.2 and 1 g/100 mL, and temperatures ranging from 30 to 50 °C. Optimal phenol removal, achieving 55.93% (0.67 mg/L), occurred at 43.40 min, 33.70 °C, and an adsorbent dosage of 0.69 g/L of textile wastewater. The phenol adsorption process using ZnO NPs was exothermic, spontaneous, and required low energy, fitting well with the Langmuir isotherm and following a pseudo-second-order kinetic model.

Enhanced removal of acidic dyes (AB1 and MO) from binary systems using anion exchange membrane BII: kinetic, isotherm, and thermodynamic analyses.

In the current work, the adsorption of acid black 1 (AB1), a hair dye, and methyl orange (MO) on anion exchange membrane BII (AEM-BII) in a binary system was studied experimentally. The effects study for contact time, adsorbent's and adsorbates' concentration, and temperature of aqueous media on the AB1 and MO removal, AEM-BII recovery, and reusability were also investigated. The highest removal was observed at optimum conditions, 150-min contact time and 5g L-1 of adsorbent for AB1 (91.2%) and MO (83.4%). Adsorption kinetics was estimated by pseudo-first-order (PFO) and pseudo-second-order (PSO) kinetics. The experimental findings were fitted well by PSO kinetics with an adsorption capacity of 19.45 ± 0.93 and 19.34 ± 0.84mgg-1 for ABI and MO, respectively. Moreover, the adsorption isotherm study confirmed that AB1 and MO adsorption by AEM-BII from the binary system was followed by Langmuir isotherms. Adsorption thermodynamics revealed that adsorption of both AB1 and MO by AEM-BII was endothermic and spontaneous. Moreover, the desorption phenomenon of ABI and MO from the loaded AEM-BII showed that dye removal from AEM-BII was found to be 74.95%, demonstrating AEM-BII can be considered as good adsorbent for acidic dyes from the binary system.

Adsorption study of methylene blue dye using activated carbon prepared from waste palm fiber.

The study investigated the utilization of waste palm fiber as an adsorbent for methylene blue (MB) removal. The waste palm fiber was treated by a series of steps to prepare an activated charcoal adsorbent. The adsorption process of MB on the activated charcoal was modeled using the Box-Behnken design (BBD) in the response surface methodology (RSM). Adsorbent mass, solution pH, temperature, and time were selected as factors, while removal efficiency and adsorption capacity were chosen as responses. Both models were significant with correlation factors of 0.85 and 0.99 for removal efficiency and adsorption capacity, respectively. Optimal conditions for MB removal were achieved at an initial pH of 7, an adsorbent dose of 0.05 g/L, and a contact time of 30 min, resulting in a 99% removal efficiency. The adsorption of MB using the activated charcoal indicates the physical nature of the reaction.

Time-dependent underwater interaction between polyhydroxyalkanoate coatings and functionalized surfaces

Polyhydroxyalkanoates (PHAs), a family of naturally occurring biodegradable polyester, are considered environmentally friendly alternatives to conventional commodity plastics derived from petrochemicals.; however, their molecular interaction in water has not been elucidated. Here, we investigated the surface- and contact time-dependent underwater interaction characteristics of poly(3-hydroxybutyrate-co-4-hydroxybutyrate) (P(3HB-co-4HB)), the most common PHA, using a surface forces apparatus (SFA). We found that PHA showed weak adhesion with functionalized surface and cohesion for a short-contact time (<30 mins) in the water. The adhesion to the functionalized surface was strong in the order of mica (negatively charged hydrophilic), APTES (positively charged hydrophilic), and PS (hydrophobic). However, the adhesive strength of PHA to the functionalized surfaces increased as contact time increased, which may be attributed to chain rearrangement, reorientation, or van der Waals forces of PHA in water. We also confirmed results similar to those for SFA by bulk testing on hydrophilic surfaces. As PHAs have attracted people’s attention as eco-friendly and biocompatible polymers, these results provide insights for the development of PHA-based composite, as well as for the biodegradation and fate of PHA post-use.

Application of porous silica supported GdFeO3 as adsorbent and photo‐Fenton catalyst for removal of rose bengal

AbstractThe synergistic effect of adsorption and photo‐Fenton process of rose bengal (RB) onto the GdFeO3‐impregnated porous silica (GFO/PS) was investigated by varying GFO loading over mesoporous silica, RB concentration, adsorbent dosage, initial pH of solution, contact time of adsorption and photo‐Fenton efficiency. The adsorption capability of RB onto GFO/PS was found to reduce by increasing the adsorbent dosage and solution pH. Meanwhile, GFO/PS photocatalyst exhibited a good performance under visible light illumination. The improvement in photo‐Fenton performance of GFO/PS could be ascribed to its large specific surface area and small band gap energy. The GFO/PS also showed good adsorption capability and high photo‐Fenton catalytic activity, suggesting it as a promising material for use to remove RB from wastewater.

Revisiting the chloramination of phenolic compounds: Formation of novel high-molecular-weight nitrogenous disinfection byproducts

Disinfection is critical for ensuring water safety; however, the potential risks posed by disinfection byproducts (DBPs) have raised public concern. Previous studies have largely focused on low-molecular-weight DBPs with one or two carbon atoms, leaving the formation of high-molecular-weight DBPs (HMW DBPs, with more than two carbon atoms) less understood. This study explores the formation of HMW DBPs during the chloramination of phenolic compounds using a novel approach that combines high-resolution mass spectrometry with density functional theory (DFT) calculations. For the first time, we identified nearly 100 previously unreported HMW nitrogenous DBPs (N-DBPs), with nearly half of those being halogenated N-DBPs. These N-DBPs were tentatively identified as heterocyclic (e.g., pyrrole and pyridine analogs) and coupling heterocyclic N-DBPs. Through detailed structure analysis and DFT calculations, the key formation steps of heterocyclic N-DBPs (monochloramine-mediated ring-opening reactions of halobenzoquinones) and new bonding mechanisms (C–N, C–O, and C–C bonding) of the coupling heterocyclic N-DBPs were elucidated. The selective formation of these novel N-DBPs was significantly influenced by factors such as contact time, monochloramine dosage, pH, and bromide concentration. Our findings emphasize the occurrence of diverse HMW heterocyclic N-DBPs, which are likely toxicologically significant, underscoring the need for further research to evaluate and mitigate their potential health risks in water disinfection.

Adsorptive removal of organophosphate pesticides from aqueous solution using electrospun carbon nanofibers.

Organophosphate pesticides (OPPs) are widely prevalent in the environment primarily due to their low cost and extensive use in agricultural lands. However, it is estimated that only about 5% of these applied pesticides reach their intended target organisms. The remaining 95% residue linger in the environment as contaminants, posing significant ecological and health risks. This underscores the need for materials capable of effectively removing, recovering, and recycling these contaminants through adsorption processes. In this research, adsorbent materials composed of electro-spun carbon nanofibers (ECNFs) derived from polyacrylonitrile was developed. The materials were characterized through several techniques, including scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Fourier Transform Infrared Spectroscopy (FTIR), Brunauer-Emmett-Teller (BET) analysis, and contact angle measurements. SEM analysis revealed details of the structural properties and inter-fiber spacing variations of the carbon nanofibers. The results revealed that ECNFs possess remarkable uniformity, active surface areas, and high efficiency for adsorption processes. The adsorption studies were conducted using batch experiments with ethion pesticide in aqueous solution. High-Performance Liquid Chromatography-Diode Array Detector (HPLC-DAD) was utilized to quantify the concentrations of the OPP. Various parameters, including adsorbent dosage, pH, contact time, and initial ethion concentration, were investigated to understand their impact on the adsorption process. The adsorption isotherm was best described by the Freundlich model, while the kinetics of adsorption followed a non-integer-order kinetics model. The adsorption capacity of the ECNFs for OPP removal highlights a significant advancement in materials designed for environmental remediation applications. This study demonstrates the potential of ECNFs to serve as effective adsorbents, contributing to the mitigation of pesticide contamination in agricultural environments.

Recent Advances in Utilizing Lignocellulosic Biomass Materials as Adsorbents for Textile Dye Removal: A Comprehensive Review.

This review embarks on a comprehensive journey, exploring the application of lignocellulosic biomass materials as highly effective adsorbents for the removal of textile dyes (cationic and anionic dyes) from wastewater. A literature review and analysis were conducted to identify existing gaps in previous research on the use of lignocellulosic biomass for dye removal. This study investigates the factors and challenges associated with dye removal methods and signifies their uses. The study delves into the pivotal role of several parameters influencing adsorption, such as contact time, pH, concentration, and temperature. It then critically examines the adsorption isotherms, unveiling the equilibrium relationship between adsorbent and dye and shedding light on the mechanisms of their interaction. The adsorption process kinetics are thoroughly investigated, and a detailed examination of the adsorbed rate of dye molecules onto lignocellulosic biomass materials is carried out. This includes a lively discussion of the pseudo-first, pseudo-second, and intra-particle diffusion models. The thermodynamic aspects of the adsorption process are also addressed, elucidating the feasibility and spontaneity of the removal process under various temperature conditions. The paper then dives into desorption studies, providing insights into the regeneration potential of lignocellulosic biomass materials for sustainable reusability. The environmental impact and cost-effectiveness of employing lignocellulosic biomass materials in textiles including Congo Red, Reactive Black 5, Direct Yellow 12, Crystal Violet, Malachite Green, Acid Yellow 99, and others dyes from wastewater treatment are discussed, emphasizing the significance of eco-friendly solutions. In summary, this review brings together a wealth of diverse studies and findings to present a comprehensive overview of lignocellulosic biomass materials as adsorbents for textile cationic and anionic dye removal, encompassing various aspects from influential parameters to kinetics, adsorption isotherms, desorption, and thermodynamics studies. Its scope and other considerations are also discussed along with its benefits. The collective knowledge synthesized in this paper is intended to contribute to the advancement of sustainable and efficient water treatment technologies in the textile industry.

Natural deep eutectic solvent-functionalized multiwall carbon nanotubes for lead removal from wastewater

In this study, two natural deep eutectic solvents (NADESs) were prepared from natural hydrogen bond donors (HBDs) based on sugar, namely fructose and sucrose, alongside H2O, and choline chloride as a hydrogen bond acceptor (HBA). The prepared NADESs were used as functionalizing agents with multiwall carbon nanotubes (MWCNTs), and the functionalized MWCNTs were used as adsorbents of Pb(II) lead ions from aqueous solution. The analyses demonstrated that MWCNTs functionalized with sucrose-based NADES to have more sub-stems and functional groups than the MWCNTs functionalized with fructose-based NADES, providing more possible sites for Pb(II) adsorption. The time dependence of Pb(II) adsorption onto these novel adsorbents was found to be better described by a pseudo-second-order kinetic model. Additionally, the Langmuir model better fits the adsorption data due to its higher coefficient of determination. Finally, the operating conditions (pH, adsorbent concentration, and contact time) were optimized using the Box-Behnken model, which demonstrated pH to exert greater influence on the adsorption process than the other studied factors. To the best of our knowledge, this study is the first to apply NADESs as emerging functionalizing agents for carbon nanomaterials in the removal of heavy metals from synthetic wastewater.

Using Sugarcane Bagasse as an Adsorbent Material to Remove Iron from Water

This study evaluates the effectiveness of chemically treated sugarcane bagasse as an adsorbent for iron removal from water. The bagasse was modified using sodium hydroxide and citric acid, and its adsorption capabilities were characterized [1-3]. Batch adsorption experiments were conducted to determine the impact of initial iron concentration, contact time, pH, and adsorbent dosage. Results indicated that the treated sugarcane bagasse exhibited a significantly higher iron adsorption capacity compared to the raw material, with an enhancement factor of 1.7. Optimal conditions were identified as a contact time of 100 minutes, a pH of 3, and an adsorbent dosage of 1.5 grams. Adsorption isotherms were best described by the Langmuir model, yielding a maximum adsorption capacity (qmax) of 15.57 mg/g. Additionally, dynamic adsorption tests showed that the adsorbent could be reused effectively, with a desorption efficiency of 75.20%. These findings demonstrate that chemically treated sugarcane bagasse is a viable, cost-effective, and environmentally friendly option for iron removal in water treatment [4].

Chitosan a Veritable Material for Removal of Some Organic Pollutants in Wastewater: An Empirical Studies

In the present study, Chitosan from cockroaches was successfully prepared, characterized by X-raydiffraction, Fourier transform infrared spectroscopy and scanning electron microscopy, and tested as adsorbent for the removal of p-Nitrophenol and Naphthalene from aqueous solutions. The influence of process variables solution pH, adsorbent dose, contact time and initial adsorbent concentration on the adsorption was evaluated. The equilibrium data was tested by Langmuir and Freundlich isotherm models for the best fit. It found the R2 values of 0.9976 for Freundlich isotherm and 0.9903 forLangmuir isotherm using Naphthalene. R2 values of 0.9843 for Freundlich isotherm and 0.739 for Langmuir isotherm. Maximum removal efficiencies of 98% for Naphthalene at the pH of 6, contact time of 2.5 h, an adsorbent dosage of 2.0 g and initial concentration of 20 mg/L. 92% for p-Nitrophenolat the pH of 6, contact time of 3.0 h, adsorbent dosage of 2.0 g and initial concentration of 60 mg/L were obtained respectively. This result shows that the prepared adsorbent has the capacity for the removal of Naphthalene and p-Nitrophenol from wastewater.

Effect of Probe Contact Resistance, Thermoelectric Voltage and Time Dependence on Electrical Resistance Measurement of Superalloy Single-Crystal Steel by Four-Point Probe

Effect of Probe Contact Resistance, Thermoelectric Voltage and Time Dependence on Electrical Resistance Measurement of Superalloy Single-Crystal Steel by Four-Point Probe

Removal of Rhodamine-B dye from Aqueous Solutions Using Alkaline-Modified Activated Carbon from Cocoa Pod Husk.

Rhodamine-B (RhB) dye in wastewater poses health and environmental risks due to respiratory and eye infections, neurotoxicity, and carcinogenicity, necessitating proper disposal for risk mitigation. This study investigates RhB removal from water using NaOH-modified activated carbon derived from cocoa pod husk (CPHAC). Employing a face-centered central composite design, operational variables were optimized to achieve maximum RhB dye removal efficiency. The study reveals a removal efficiency of 98.87 ± 0.84% under optimized conditions: adsorbent dose of 1.34g, contact time of 71.59min, and an initial RhB concentration of 6.61 ppm. The Freundlich isotherm model demonstrated a good fit, suggesting that RhB removal is governed by heterogeneity and multilayer adsorption. Kinetic experiments revealed that adsorption follows a pseudo-second-order model, indicating likely irreversible adsorption with dye molecules forming chemical bonds on CPHAC's surface. Overall, this study demonstrates the effectiveness of CPHAC as an efficient adsorbent for RhB removal from water.