Adsorption Of Methylene Blue Dye Research Articles

Synthesis of chitosan-graphene oxide (GO) composite using the sol-gel method and its application in the adsorption of methylene blue dye

Synthesis of chitosan-GO composites using the sol-gel method and its application to methylene blue adsorption has been carried out. This study aims to determine the ability of chitosan-GO composites to adsorb methylene blue. Chitosan-GO composites were made with mass ratios (1:1), (1:3), and (1:5) and characterized by XRD. Material with a ratio (1:1) was chosen to be characterized using BET, SEM-EDS, and used as methylene blue adsorption. Methylene blue adsorption process with several variables including contact time, concentration, and temperature of methylene blue dye. The results of the XRD characterization of the chitosan-GO composite (1:1), (1:3), and (1:5) showed a diffraction peak at an angle of 2θ, namely 25.1°; 26.29° and 19.54°. The surface area of the chitosan-GO composite (1:1) with BET was 145.3505 m2/g. Characterization using SEM showed that the chitosan-GO (1:1) composite had a porous structure and was not homogeneous. Optimum conditions for the adsorption of the chitosan-GO composite on methylene blue were obtained at 50 minutes contact time, concentration of 60 ppm, and at 50°C. The adsorption process of the chitosan-GO composite on methylene blue followed the Freundlich adsorption isotherm with an adsorption capacity of 2.47 mg/g.

Nanoarchitectonics of hydrothermal carbonized sugarcane juice-derived biochar for high supercapacitance and dye adsorption performance

Here, we report the exfoliation of micron-sphere biochar to a few layers using the conventional KOH activation process. Micron-sphere biochar is obtained from hydrothermal carbonization (HTC) of sugarcane juice (Saccharum officinarum). HR-TEM and Raman spectroscopy studies revealed the conversion of micron-sphere biochar (MSB) to a few layers of biochar (FLB) in the activation process. BET characterization revealed FLB with a high surface area of 681.21 m2/g having mesopores. Consequently, an electrochemical study demonstrated excellent supercapacitor performance with a specific capacitance of 964.5 F/g and an energy density of 33.11 Wh/kg at a maximum power density of 936 W/kg. Batch adsorption studies showed rapid Methylene blue (MB) dye adsorption in 10 min. The equilibrium data analysis indicated the Langmuir adsorption isotherm with a correlation coefficient of 0.99. Evaluation of the kinetic models suggests that pseudo-second-order kinetics is the most appropriate model, implying that the adsorption of MB dye is primarily due to chemisorption. These findings suggest a Nanoarchitectonics of biochar into a few layers using traditional KOH activation, suitable for various applications.

Application of Optimization Response Surface for the Adsorption of Methylene Blue Dye onto Zinc-coated Activated Carbon.

The activated carbon was produced in the first phase of this investigation by chemically activating hazelnut shell waste with H3PO4. Composite materials were obtained by coating the activated carbon with zinc oxide, whose BET surface area was calculated as 1278 m2 g-1. ZnO-doped ZnO/AC composite was synthesized as an adsorbent for its possible application in the elimination of organic dyestuff MB, and its removal efficiency was investigated. Morphological properties of ZnO/AC were characterized using analytical methods such as XRD, SEM, and BET. The adsorption system and its parameters were investigated and modeled using the response surface method of batch adsorption experiments. The experimental design consisted of three levels of pH (3, 6.5, and 10), initial MB concentration (50, 100, and 150 mg L-1), dosage (0.1, 0.3, and 0.5 g 100 mL-1), and contact time (5, 50, and 95 min). The results from the RSM suggested that the MB removal efficiency was 98.7% under the optimum conditions of the experimental factors. The R2 value, which expresses the significance of the model, was determined as 99.05%. Adsorption studies showed that the equilibrium data fit well with the Langmuir isotherm model compared to Freundlich. The maximum adsorption capacity was calculated as 270.70 mg g-1.

Unveiling the Nature of lignin's Interaction with Molecules: A Mechanistic Understanding of Adsorption of Methylene Blue Dye.

The valorization of lignin into advanced materials for water and soil remediation is experiencing a surge in demand. However, it is imperative that material research and manufacturing be sustainable to prevent exacerbating environmental issues. Meeting these requirements necessitates a deeper understanding of the role of lignin's functional groups in attracting targeted species. This research delves into the interaction mechanisms between lignin and organic molecules, using the adsorption of the cationic dye Methylene Blue (MB+) as a case study. Herein, we aim to quantitatively estimate the contribution of different interaction types to the overall adsorption process. While carbonyl groups were found to have no significant role in attraction, carboxylic groups (-COOH) exhibited significantly lower adsorption compared with hydroxyl groups (-OH). Through alternately blocking aliphatic and phenolic -OH groups, we determined that 61% of the adsorption occurred through hydrogen bonding and 38% via electrostatic interactions. Performance studies of modified lignin along with spectroscopic methods (XPS, FTIR) confirmed the negligible role of π-π interactions in adsorption. This study offers fundamental insights into the mechanistic aspects of MB adsorption on lignin, laying the groundwork for potential modifications to enhance the performance of lignin-based adsorbents. The findings underscore the importance of hydroxyl groups and provide a roadmap for future studies examining the influence of steric factors and interactions with other organic molecules.

Tunable dye adsorbing materials from crab and shrimp waste shells for water remediation

Crab and shrimp shells are waste byproducts from shellfish farming and processing. In this study, we demonstrated that it is possible to obtain individual shell components either separately or in combinations. These diverse materials were composed of calcium carbonate and organic molecules inter- and intra-mineral, calcium carbonate and organic molecules intra-mineral, organic molecules such as chitin and proteins, only calcium carbonate, and only chitin. These substrates were tested for the adsorption of Methylene Blue and Eosin dyes. The goal is to demonstrate that the organic dye adsorption capacity can be modified by controlling the degree of deconstruction of the starting material. The best adsorption for the positively charged Methylene Blue was achieved on the chitin-calcium carbonate substrates, while the negatively charged Eosin adsorbed best on the chitin substrate. In conclusion, this research demonstrates that it is possible to obtain different materials by deconstructing the shells from crabs and shrimps at various levels reducing the generation of additional wastes. Moreover, these materials exhibit features that are related to the original material and possess new properties that can be also exploited in other fields like material sciences.

Design and preparation of a novel Mg-Al LDH@EDTA-Melamine nanocomposite for effective adsorptive removal of methylene blue and rhodamine B dyes from water

This paper deals with the preparation of a novel nanocomposite consisted of magnesium-aluminum layered double hydroxide (Mg-Al LDH) and ethylenediaminetetraacetic acid (EDTA) as well as melamine (MA) as an adsorbent. This nanocomposite was utilized to adsorb different dyes such as rhodamine B (RhB) and methylene blue (MB) from water. The prepared adsorbent was characterized using FT-IR, EDS, XRD, TGA, and FE-SEM analyses. The effects of various parameters such as concentration, time, adsorbent dosage, temperature, and pH were tested to investigate their influence on adsorption conditions. Both methylene blue and rhodamine B dyes showed pseudo-second-order adsorption kinetics, and their adsorption followed the Langmuir isotherm. Moreover, the maximum adsorption capacities for methylene blue and rhodamine B were found to be 1111.103 mg/g at 45 °C and 232.558 mg/g at 60 °C, respectively. Additionally, the adsorption processes were found to be spontaneous (ΔG°< 0, for both dyes) and exothermic (ΔH°= -12.42 KJ/mol for methylene blue and ΔH°= -25.84 KJ/mol for rhodamine B) for both dyes. Hydrogen bonding and electrostatic forces are responsible for the interactions occur between the nanocomposite and the functional groups in the dyes. The experimental findings demonstrated a greater adsorption rate of MB than RhB, suggesting the adsorbent's stronger affinity for MB. This preference is likely due to MB's size, specific functional groups, and smaller molecule size, enabling stronger interactions and more efficient access to adsorption sites compared to RhB. Even after recycling 4 times, the dye adsorption percentages of the adsorbent for MB and RhB dyes were 90% and 87%, but the desorption percentages of the adsorbate dyes were 85% and 80%, respectively. The prepared adsorbent boasts several unique properties, such as the swift and effortless adsorption of MB and RhB dyes, straightforward synthesis, mild adsorption conditions, remarkable efficiency, and the ability to be recycled up to 4 times without a significant decrease in activity.

Hybrid rGO/Fe3O4 magnetic nanocomposite for anionic and cationic dye removal application

The adsorption removal of anionic and cationic azo dyes with magnetic nanoparticles was an important technological strategy for the purification of dye-contaminated water. The present work highlights the dye adsorption properties of the solvothermally synthesized hybrid reduced graphene oxide‑iron oxide (rGO/Fe3O4) nanocomposite for the efficient adsorption of methyl orange, congo red, metanil yellow, and methylene blue from the aqueous medium. Morphology, and porous characteristics of the material was analysed with FESEM and BET respectively. The magnetic properties of the material viz. M-H, FC, and ZFC were investigated with SQUID-VSM. The BET analysis confirmed the mesoporous structure of the hybrid rGO/Fe3O4 nanocomposite, with a BET-specific surface area of 27.74 m2/g. Dye adsorption experiments of hybrid rGO/Fe3O4 nanocomposite were conducted to analyse the influence of adsorbent dosage, dye concentrations, and pH variations. FTIR spectroscopy was also used to verify the adsorption of azo dyes onto the surface of the rGO/Fe3O4 nanocomposite. Hybrid rGO/Fe3O4 nanocomposite show complete adsorption of methyl orange, congo red, metanil yellow, and methylene blue dyes with adsorption capacities of 58.76, 100.3, 533, and 50 mg/g, respectively in the water medium. Hybrid rGO/Fe3O4 nanocomposite showed excellent adsorption of metanil yellow dye. The adsorbed azo dyes methyl orange, metanil yellow, methylene blue, and congo red by the rGO/Fe3O4 nanocomposite can be easily desorbs from the material indicating its reusability. The magnetic coercivity of the material at 300K was 47.4 Oe, as a result the adsorbent material can be magnetically separated from the purification system. The adsorption process of methyl orange, congo red, metanil yellow, and methylene blue dyes on the rGO/Fe3O4 nanocomposite best fits to the pseudo-second-order kinetics and the Langmuir isotherm model.

Optimizing Methylene Blue Dye Adsorption onto Liquid Natural Rubber-Based Hydrogel: Kinetics, Isotherms and Reusability

In recent years, notable advancements have taken place in the textile industry, particularly with the widespread use of synthetic dyes such as methylene blue (MB). However, the environmental impact of these dyes has raised significant concerns. Their potential to influence both chemical and biochemical demand poses risks, leading to potential disruptions in aquatic plant photosynthesis. Additionally, concerns exist regarding the toxicity and potential carcinogenicity of these dyes to humans. This study achieved successful hydrogel synthesis through the efficient utilization of ultrasonic methods, combining liquid natural rubber (LNR), acrylic acid (AAc), and pectin (Pc) to adsorb MB from aqueous solutions. Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM) were employed to analyze the structure. Utilizing Response Surface Methodology (RSM), the study investigated the effects of the AAc:LNR weight ratio and Pc weight on hydrogel preparation for MB removal. This led to the development of a quadratic polynomial model with an ANOVA-derived R2 value of 0.9970. Optimal conditions for hydrogel production were identified as a 3.00 g/g AAc:LNR weight ratio and 0.0325g of Pc, resulting in an impressive 99.07% MB removal effectiveness. The limit of detection (LOD) for methylene blue adsorption was calculated at 0.64 ppm. The kinetics and isotherms of MB removal were described by the pseudo-second-order and Freundlich models, respectively. Furthermore, the investigation into hydrogel reusability demonstrated its capability for up to five utilization cycles. The LNR/AAc/Pc hydrogel exhibits promising potential as an effective, cost-efficient, and environmentally conscious adsorbent for MB removal. This makes it applicable to water treatment scenarios involving cationic dyes.

Kinetic study of adsorption and photocatalytic degradation of methylene blue dye using TiO2 nanoparticles with activated carbon

Activated carbon (AC) exhibits limited adsorption capacity for pollutants. Conversely, titanium dioxide (TiO2) demonstrates excellent photocatalytic performance, making it a popular choice for pollutant removal. This study investigates the removal of methylene blue (MB) dye from wastewater using AC, TiO2@AC-2, and TiO2@AC-10 samples via adsorption and photocatalysis. The Energy Dispersive analysis of x-rays (EDAX) has confirmed the presence of Ti, C and O in the prepared samples without any impurities. All the diffraction peaks in x-ray diffractograms indicated the presence of pure anatase TiO2 (tetragonal phase) with no evidence of any other phase. Fourier transform infrared spectroscopy (FTIR) analysis identified a peak around 545 cm−1 in the TiO2@AC-2 sample, indicative of O-Ti-O stretching vibrations. This peak shifted to 602 cm−1 in the TiO2@AC-10 sample. Raman spectroscopy confirmed the presence of carbon (D and G bands) at 1310–1347 cm−1 and 1582–1597 cm−1. Additionally, characteristic Raman active bands for anatase TiO2 were observed at 154 cm−1 (Eg), 204 cm−1 (Eg), 398 cm−1 (B1g), 508 cm−1 (A1g), and 628 cm−1 (Eg). N2 adsorption–desorption isotherms revealed a mesoporous structure for all samples (AC, TiO2@AC-2, and TiO2@AC-10) with hysteresis loops, indicating pores ranging from 2 nm to 50 nm in diameter. Reflectance spectra of TiO2@AC-2 and TiO2@AC-10 displayed absorption edges at 368 nm and 385 nm, respectively, corresponding to a direct band gap of approximately 3.22 eV. Subsequently, these prepared samples were effectively employed for the removal of methylene blue (MB) dye from wastewater utilizing both adsorption and photocatalysis method. Under dark conditions, 20 mg L−1 doses of TiO2@AC-2 and TiO2@AC-10 resulted in 60% and 36% dye adsorption within 60 min respectively. In the presence of UV radiation, the degradation of dye was observed to be 74% and 95% by TiO2@AC-2 and TiO2@AC-10 respectively. This observation indicates that TiO2 nanoparticles along with AC leads to enhanced photocatalytic activity. The Langmuir–Hinshelwood model reveals lower rate constants for AC compared to the composite samples. This is likely because AC lacks inherent catalytic activity, requiring UV light to trigger adsorption. Conversely, TiO2@AC-10 exhibits the highest rate constants (K1 = 24.25 × 10−3 min−1 and K2 = 82.71 × 10−3 min−1), aligning with its higher TiO2 content confirmed by EDAX analysis. This suggests a significantly faster photocatalytic rate and superior degradation efficiency, even at a low sample concentration (20 mg L−1).

Investigation of kinetics and thermodynamics of methylene blue dye adsorption using activated carbon derived from bamboo biomass

This research paper aimed to evaluate the potential of activated carbon (AC) made from non-torrefied and torrefied bamboo biochar samples for the purpose of adsorbing methylene blue solution. The process involved impregnating bamboo biochar with a 5 M potassium hydroxide (KOH) solution at a 1:4 ratio of biochar to KOH, followed by carbonization at 800 °C, 900 °C, and 1000 °C to produce activated carbon samples. The samples were then characterized using techniques such as XRD, FESEM-EDX, FTIR, FE-TEM, and BET analysis to study their respective phase, surface morphology, elemental composition, functional groups, and structural and surface properties. The results showed that the torrefied bamboo AC exhibited a specific surface area of 366 m2/g and a total pore volume of 0.24 m3/g. Kinetic analyses showed adsorption following a pseudo-second-order model, with a capacity of 83.3 mg/g according to the Langmuir model and a favorability constant of 0.52 from the Freundlich model. Thermodynamic studies revealed the process to be spontaneous and endothermic, with changes in enthalpy and entropy of 77,810.73 kJ/mol and 269.9 kJ/mol·K, respectively. These findings highlight the effectiveness of bamboo-derived AC as a sustainable adsorbent for MB dye removal, offering a promising solution for water pollution control.

Production and Characterization of Activated Carbon Derived from Costus Afer Leaves (C. afer) for the Adsorption of Methylene Blue Dye from an Aqueous Solution

In this work, Costus afer leaves (C. after) was utilized as an agricultural waste material for the synthesis of activated carbon (AC) used for the adsorption of methylene blue dye from its aqueous solution. The raw material was prepared, chemically activated using KHCO3 with an impregnation ratio of 1:3, and later carbonized at a temperature of 700℃ in an inert N2 atmosphere for 1hour to produce activated carbon. The proximate analysis of the biomass revealed the percentage of ash content, moisture content, volatile matter, and fixed carbon present in the waste biomass. The raw and activated carbon produced were characterized using various tests such as: Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray (EDX), Fourier Transform Infrared-(FTIR) Spectrometry, X-Ray Fluorescence (XRF), and Brunauer-Emmett-Teller (BET). The results revealed that the SBET of the biomass increased from 400m2/g to 600m2/g after activation. Adsorption studies were carried out in batch mode to determine the influencing factors of adsorption with varying adsorbent dosage, contact time, and pH values. The adsorption experiment revealed high adsorption efficiency at an optimum parameter of dosage (0.2g), contact time (10 min), and pH (8) with a 70.58% removal of methylene blue dye. An increase in dosage, contact time, and pH above the optimum parameter leads to a decrease in percentage removal. The adsorption capacity was achieved using adsorption isotherm models like Langmuir and Freundlich. Adsorption of methylene blue validated the Langmuir model with an R2 of 0.999 and a Qm of 11.83 mg/g. These results show that activated carbon prepared from Costus afer leaves constitutes an effective low-cost material for the adsorption of Methylene dye from wastewater.

Blended Nephelium lappaceum and Durio zibethinus wastes for activated carbon production via microwave-ZnCl2 activation: optimization for methylene blue dye removal

Herein, this work targets to employ the blended fruit wastes including rambutan (Nephelium lappaceum) peel and durian (Durio zibethinus) seed as a promising precursor to produce activated carbon (RPDSAC). The generation of RPDSAC was accomplished through a rapid and practical procedure (microwave-ZnCl2 activation). To evaluate the adsorptive capabilities of RPDSAC, its efficacy in eliminating methylene blue (MB), a simulated cationic dye, was measured. The Box–Behnken design (BBD) was utilized to optimize the crucial adsorption parameters, namely A: RPDSAC dose (0.02–01 g/100 mL), B: pH (4–10), and C: time (2–6 min). The BBD design determined that the highest level of MB removal (79.4%) was achieved with the condition dosage of RPDSAC at 0.1 g/100 mL, contact time (6 min), and pH (10). The adsorption isotherm data is consistent with the Freundlich concept, and the pseudo-second-order versions adequately describe the kinetic data. The monolayer adsorption capacity (qmax ) of RPDSAC reached 120.4 mg/g at 25 °C. Various adsorption mechanisms are involved in the adsorption of MB dye onto the surface of RPDSAC, including π–π stacking, H-bonding, pore filling, and electrostatic forces. This study exhibits the potential of the RPDSAC as an adsorbent for removal of toxic cationic dye (MB) from contaminated wastewater.

Tailoring electrospun nanocomposite fibers of polylactic acid for seamless methylene blue dye adsorption applications.

The introduction of biopolymers, which are sustainable and green materials, desegregated nature's water purification proficiency with science and technology, opens a new sustainable methodology in water reclamation. In order to introduce an efficacious adsorbent system for MB dye-toxic pollutant, adsorption, providing robust mechanical properties and facile processability, a facile system was introduced via electrospinning utilizing polylactic acid (PLA) and Ti3C2Tx, viz., PMX. The addition of 3 wt.% Ti3C2Tx led to a 3-fold substantial augmentation in the uptake capacity of the membrane from 197.28 to 307 mg/g when the adsorbate concentration was 100 ppm. The adsorption followed a PSO behavior, proposing that the rate-limiting stage is chemisorption and data best fitted to Freundlich isotherm, indicating heterogeneous adsorption sites and multi-layer adsorption. Further, biodegradability was studied by simulating natural environmental conditions where the nanofibers exhibited 42-64% degradation after 270 days. Based on the result with PLA, it is anticipated that the prepared fibrous system will introduce a new perspective as a potential candidate for MB removal from wastewater, opening new directions toward the research and development in wastewater treatment with electrospun biopolymer fibers using waste PLA.

Exploring the potential of olive pomace derived activated charcoal as an efficient adsorbent for methylene blue dye: a comprehensive investigation of isotherms, kinetics, and thermodynamics

Methylene blue (MB) is a heterocyclic aromatic chemical compound used as a dye in various dyeing processes. The accumulation of such an organic compound poses a significant threat to both the environment and human health. Therefore, numerous biological, physical, and chemical processes have been established to remove MB dye, with adsorption being the most predominant dye-based treatment technology. In this context, the aim of this work was to evaluate the adsorption properties of activated carbon derived from olive pomace against methylene blue. To this end, scanning electron microscopy (SEM), energy dispersive x-ray spectroscopy (EDS), and Fourier transform infrared spectroscopy (FT-IR) analyses were carried out to confirm the adsorption of MB on carbon structures. In addition, the effect of contact time, pH, initial dye concentration, adsorbent dose, and temperature on the adsorption efficiency of MB was investigated. On the other hand, kinetic and isothermal models were used to further understand the adsorption mechanism, which showed a good correlation with the pseudo-second-order kinetic model and the Langmuir isotherm. Finally, thermodynamic analysis showed favorable conditions for physisorption, with the process being both endothermic and spontaneous.

Enhanced adsorption capacity of phosphoric acid-modified montmorillonite clay and ground coffee waste-derived carbon-based functional composite beads for the effective removal of methylene blue

Clays, valued for their versatility, serve as economical adsorbents. Recent studies show that physical, thermal, and chemical modifications can enhance their adsorption capacity. In this study, the synthesis of a functional bead comprising phosphoric acid-modified montmorillonite (PMMT) and coffee waste carbon (CWC) and its application for the efficient adsorption of methylene blue (MeB) dye is investigated. A highly flexible and low-cost phyllosilicate, montmorillonite clay, MMT was treated with phosphoric acid to enhance the ionic density, composited with CWC, resulting in improved surface properties thereafter was transformed into easily recoverable bead form through subsequent cross-linking steps. These functional composite beads were characterized using various characterization techniques. As a result, the existing tetrahedral sheets possessed by the MMT having weak bonds between the layers are improved in a way that they can allow molecule exchange for the efficient enhancement of the adsorption capacity of the composite material. Moreover, after the necessary modifications, the adsorbent was found to be mechanically stable, inhibiting secondary pollutions from the use in powder forms while allowing the interlayers favorable for not just cationic but also anionic exchange whilst increasing the specific surface area and pore volume. The surface area was enhanced to 9.93 m2 /g. Following this, maximum adsorption capacity of 489.9 mg/g was attained showing a superior removal efficiency for methylene blue dye (>80%). The adsorption equilibrium was analyzed using Freundlich and Langmuir models. The adsorption mechanism aligns with the Langmuir model which encompasses a monolayer adsorption. All in all, this study is anticipated to play a crucial role in the search for adsorbents with multiple functionalities and good structural stability during and after use.

Decolourization of Methylene Blue by using Eucalyptus Globulus Leaf Powder as a Adsorbent

In the present study, the feasibility of using low-cost adsorbent Eucalyptus Globulus leaf powder for the cationic dyes adsorption from aqueous solutions have been investigated. Batch adsorption studies are conducted to study conducted to the different parameters are adsorbent dosage of 2-20 g/L, initial dye concentration of 50-250 mg /L, Temperature of 293oK, 303 oK and 313 oK on adsorption of methylene blue dye at equilibrium time of 80 minutes respectively and optimal pH of 5.0. The equilibrium data is analysed with isotherm models are Langmuir and Freundlich and kinetic models are Pseudo-first order, Pseudo-second order model. The adsorption equilibrium and kinetic data fitted well to Freundlich isotherm model for methylene blue dye and Pseudo-second order model for methylene blue dyes. The adsorption is an Endothermic and it is energetically favourable adsorption. The result demonstrates that Eucalyptus Globulus leaf powder could be employed as effective and low-cost adsorbent for the removal of methylene blue and from aqueous solutions.

Effect of the Photoreduction Process on the Self-Cleaning and Antibacterial Activity of Au-Doped TiO2 Colloids on Cotton Fabric.

This study aims at understanding the effect of the photoreduction process during the synthesis of gold (Au)-doped TiO2 colloids on the conferred functionalities on cotton fabrics. TiO2/Au and TiO2/Au/SiO2 colloids were synthesized through the sol-gel method with and without undergoing the photoreduction step based on different molar ratios of Au:Ti (0.001 and 0.01) and TiO2/SiO2 (1:1 and 1:2.3). The colloids were applied to cotton fabrics, and the obtained photocatalytic self-cleaning, wet photocatalytic activity, UV protection, and antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria were investigated. The obtained results demonstrated that the photoreduction of Au weakened the self-cleaning effect and reduced the photocatalytic activity of coated fabrics. Also, an excess amount of Au deteriorated the photocatalytic activity under both UV and visible light. The most efficient self-cleaning effect was obtained on fabrics coated with a ternary TiO2/Au/SiO2 colloid containing ionic Au, where it decomposed coffee and red-wine stains after 3 h of illumination. Adding silica (SiO2) made the fabrics superhydrophilic and led to greater methylene blue (MB) dye adsorption, a faster dye degradation pace, and more efficient stain removal. Moreover, the photoreduction process affected the size of Au nanoparticles (NPs), weakened the antibacterial activity of fabrics against both types of tested bacteria, and modestly increased the UV protection. In general, the photoactivity of Au-doped colloids was influenced by the synthesis method, the ionic and metallic states of the Au dopant, the concentration of the Au dopant, and the presence and concentration of silica.

By-product Eucalyptus leaves valorization in the basic dye adsorption: kinetic equilibrium and thermodynamic study

Abstract Algerian Eucalyptus Leaves (AEL), a natural biodegradable adsorbent abundantly available, was used for the removal of methylene blue (MB) dye. The AEL properties for the removal of MB were investigated under different conditions by varying the AEL amount, MB concentration, pH of the solution and the reaction temperature. Scanning electron microscopy (SEM) and infrared spectroscopy (FTIR) techniques have been used to characterize AEL biosorbent. Experimental results showed that the adsorption of MB dye at the concentration of 50 mg L−1 reached to 91 % at pH 10 with a stirring speed of 200 rpm and after 180 min of reaction time. The experimental data were analyzed using the linear forms of different kinetic models (pseudo-first order kinetic model, pseudo-second order kinetic model, and intra-particle diffusion models). The results demonstrated that the adsorption kinetics of MB was consistent with the pseudo-second order model with R 2 value of 0.9969. The isotherm models Langmuir, Freundlich, Dubinin, Elovich, Brunaut Emmet Teller and Temkin models were also investigated to describe the adsorption equilibrium. The results show that the AEL adsorption is in accordance with Temkin isotherm. The thermodynamic study revealed that the adsorption is spontaneous and exothermic. Therefore, as a cheap green adsorbent with high MB adsorption performance, AEL is expected to become one of the best candidate materials for future industrial wastewater treatment.

Ultrasonic-Assisted Nitrate Anion Incorporation in Triaminoguanidium Chloride Based Covalent Organic Polymer for Methylene Blue Dye Adsorption.

Terephthalaldehyde-triaminoguanidium chloride covalent organic polymer, Te-TGCl COP can facilely be incorporated with NaNO3 by sonication. Te-TGCl COP incorporated with NaNO3 via ultrasonication adsorbs Methylene Blue (MB) dye. Te-TGCl COP alone shows negligible adsorption capacity for MB, however, when treated with NaNO3, its adsorption capacity emerges slightly. Moreover, ultrasonication of the NaNO3 treated COP, Te-TG-NaNO3 COP shows dramatic increase in its adsorption capacity for MB (qe for Te-TGCl COP ≈0 mg g-1; for Te-TG-NaNO3=17.65 mg g-1). Emergence of MB dye adsorption property in Te-TG-NaNO3 COP composite may be attributed primarily to the electrostatic interaction of MB dye molecules with nitrate anions and the sonochemical effect caused fibrous morphological structure of the adsorbent material. The kinetics of MB dye adsorption onto Te-TG-NaNO3 COP composite exhibits an excellent fit for the pseudo-second order model, suggesting the rate-determining step to be chemisorption. Homogeneous monolayer adsorption of MB dye onto Te-TG-NaNO3 COP composite can be suggested as the Langmuir isotherm model seemed to be fitted well.

Carbon encapsulated ZnO nanoplates for efficient removal of organic dyes from aqueous medium by adsorption: Role of organic ligand and calcination temperature

Water pollution by organic dyes poses great challenge to the environment as well as living organisms. Herein, we have fabricated nanoplates of ZnO in carbon matrix by controlled calcination of zinc-metal organic frameworks (Zn-MOFs) and used as adsorbents for efficient removal of organic dyes from water. Zn-MOF of phthalic acid and 5-nitrophthalic acid produced nanoplates of ZnO (ZnO-C and ZnO-NC) in carbon matrix without and with nitrogen doping. The fabricated hybrid nanostructures were characterized using PXRD, FTIR, BET, TGA, HR-SEM, HR-TEM and XPS analysis. Both ZnO-C and ZnO-NC showed high adsorption of cationic dyes (crystal violet (CV), methylene blue (MB) and Rhodamine B (Rh B)) compared to anionic dyes (methyl orange (MO) and Eosin yellow (EY)). Nitrogen doped ZnO-NC exhibited relatively higher percentage of dyes removal (99 %) compared to ZnO-C. Interestingly, ZnO-NC showed high adsorption of MB dye across the pH range from acidic (pH = 3.0) to alkaline (pH = 11.0). The zero-point charge indicated the negative surface charge for ZnO-NC/ZnO-C that facilitated electrostatic interactions between dyes and adsorbents. Adsorption kinetics suggested a pseudo second order model and adsorption isotherm fitted well with the Freundlich model, suggesting heterogenous adsorption with multilayer coverage of dye molecules. The reusability of ZnO-NC showed only slight reduction of adsorption in three successive cycles. Further, ZnO-NC was used as column packing materials for the successful removal of both cationic as well as anionic dyes upon filtration. Thus, the present studies provided insight on the organic ligand structure and calcination temperature of MOFs for transforming them into effective organic dye adsorbent.