Biosorption of Direct Yellow 12 from aqueous solution using green alga Ulva lactuca

The potential of commonly available green alga Ulva lactuca was investigated as viable biomaterials for removal of synthetic azo dye (Direct Yellow 12, DY-12) from aqueous solution. The results obtained from the batch experiments revealed that the ability of the U. lactuca to remove DY-12 from its aqueous solution was dependent on the dye concentration, pH, and algal biomass but less dependent on the particle size of the U. lactuca. The equilibrium conditions and kinetics of adsorption were investigated, and the adsorption kinetic was consistent with the pseudo-second-order model (R²=1). The adsorption isotherm followed only the Freundlich model with a correlation coefficient R²=0.99. This study demonstrated that the U. lactuca could be used as an effective biosorbent for the removal of DY-12 from its aqueous solution.     

Pomegranate husk as an adsorbent in the removal of toxic chromium from wastewater

The use of a new sorbent developed from the husk of pomegranate, a famous fruit in Egypt, for the removal of toxic chromium from aqueous solution has been investigated. The batch experiment was conducted to determine the adsorption capacity of the pomegranate husk. The effects of initial metal concentration (25 and 50 mg l^-1), pH, contact time, and sorbent concentration (2-6 g l^-1) have been studied at room temperature. A strong dependence of the adsorption capacity on pH was observed, the capacity increased as the pH decreased, and the optimum pH value was pH 1.0. Adsorption equilibrium and kinetics were studied with different sorbent and metal concentrations. The adsorption process was fast, and equilibrium was reached within 3 h. The maximum removal was 100% for 25 mg l^-1 of Cr⁶⁺ concentration on 5 g l^-1 pomegranate husk concentration, and the maximum adsorption capacity was 10.59 mg g^-1. The kinetic data were analysed using various kinetic models—pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion equations—and the equilibrium data were tested using several isotherm models, Langmuir, Freundlich, Tempkin, Dubinin-Radushkevich, and Generalized isotherm equations. The Elovich and pseudo-second-order equations provided the greatest accuracy for the kinetic data, while Langmuir and Generalized isotherm models were the closest fit for the equilibrium data. The activation energy of sorption has also been evaluated as 0.236 and 0.707 kJ mol^-1 for 25 and 50 mg l^-1 chromium concentration, respectively.     

Mass-transfer processes of chromium(VI) adsorption onto guava seeds

The chromium(VI) biosorption onto guava seeds, as an alternative method for Cr⁶⁺ removal from aqueous solutions, was investigated. The parameters affecting kinetics and equilibrium of Cr⁶⁺ adsorption onto guava seeds were studied. An external mass-transfer diffusion coefficient k and intra-particle diffusion coefficient k_i were determined to measure the rate-limiting step of adsorption. A single external mass-transfer diffusion model and intra-particle diffusion models were used. The effects of initial pH, sorbent mass, and initial Cr⁶⁺ concentrations on mass-transfer coefficients were investigated. The external mass-transfer coefficient has an average value of 7.2×10^-3 cm s^-1, while the intra-particle mass-transfer diffusion coefficient was 0.34 mg g^-1 min^-0.5. This indicates that external diffusion to the guava seeds surface and intra-particle diffusion are both involved in the sorption process. The isotherm equilibrium data were well fitted by the Langmuir and Freundlich models with an average correlation coefficient R²=0.98. The maximum removal of Cr⁶⁺ was obtained at pH 1 (about 100% for adsorbent dose of 15 g l^-1 and 25 mg l^-1 initial concentration of Cr⁶⁺). The results indicated that the guava seeds exhibit acceptable sorption capacity.     

Dissolved trace-metal concentrations along the Mediterranean Sea, to the north of the Nile Delta Region, Egypt

This work focuses on four marine sites of the Mediterranean Sea, north of the Nile Delta, Egypt. Surface-water samples were collected seasonally during 2003. The aim of this study is to assess the levels of some dissolved trace metals (Fe, Mn, Zn, Cu, and Pb) in two environmental conditions. The metal concentrations in the coastal zone were in the following ranges: 11.92-30.45 μg l^-1 for Fe, 5.79-17.36 μg l^-1 for Mn, 0.87-7.80 μg l^-1 for Zn, 0.40-1.87 μg l^-1 for Cu, and 1.53-10.31 μg l^-1 for Pb. In the sites with continental water input (mixing zone), the metals were scattered in the following ranges: Fe (19.72-60.33 μg l^-1), Mn (12.63-35.60 μg l^-1), Zn (2.67-22.00), Cu (0.83-8.10 μg l^-1), and Pb (1.72-29.7 μg l^-1). The results for the metal concentrations showed a remarkable decrease in the levels of the different metals going from the estuaries and outlets into the coastal sea water. Generally, the levels of the metals in the two zones are higher than the background levels of the unpolluted area. A comparison of the trace-metal levels in the coastal zone of the Mediterranean Sea north of Nile Delta with the minimal risk concentration (reported by water-quality criteria, WQC) showed a significantly lower content at the coastal area of the Mediterranean sea of Egypt. The study also indicated that the impact of anthropogenic inputs was limited in the distribution of the metals, except that the Pb content was slightly higher in the area of the mixing zone than that reported for WQC. The relationships between the different trace-metal concentrations and the other parameters (salinity, chlorophyll a and suspended particulate matter) were discussed, and the simple regressions between them were evaluated.     

Hydrochemistry and dissolved nutrient flux of two small catchment rivers, south-western India

This paper deals with the water chemistry and dissolved nutrient flux of two small mountainous and heavily dammed rivers—Periyar and Chalakudy—of Kerala on the south-west coast of India. The lower reaches of these rivers are affected by sea-water ingression from the Arabian Sea during the non-monsoon season. Human interference through agriculture, urbanization, and industrialization in the lower and middle stretches of the river basins induces marked concentration variations in the hydro-chemical parameters. Except for N & P, all other chemical constituents exhibit high values during the non-monsoon season. Industrial contaminants in specific locations of the Periyar river reduce the pH to lower levels. Nutrients in the two rivers reveal marked seasonal and regional concentration variations. During the monsoon season, dissolved inorganic nitrogen (DIN) predominates over dissolved organic nitrogen (DON), but the reverse trend is observed during the non-monsoon season. The Periyar river shows higher average concentrations of DIN (monsoon 801 μg l^-1 and non-monsoon 292 μg l^-1) than Chalakudy river (monsoon 478 μg l^-1 and non-monsoon 130 μg l^-1). Dissolved inorganic phosphorus (DIP) has lower average values in the monsoon season (Periyar river, 38 μg l^-1; Chalakudy river, 42 μg l^-1) than dissolved organic phosphorus (DOP) values (Periyar river, 107 μg l^-1; Chalakudy, 62 μg l^-1). The rivers show a marked difference in nutrient flux due to its difference in water discharge/basin characteristics and point/non-point sources of contaminants. The flux rates of DIN, DIP, and DOP during the monsoon are higher than during the non-monsoon season, while those of dissolved silicon (DSi), dissolved Fe (DFe), and DON are lower. On average, the Periyar river discharges 4953 t y^-1 of DIN and 1626 t y^-1 of DON to the coastal waters, and the corres-ponding values of the Chalakudy river are 772 t y^-1 and 596 t y^-1. The Periyar and Chalakudy rivers discharge 245 t y^-1 and 70.8 t y^-1 of DIP, respectively. The total flux of DOP is considerably higher (Periyar river 703 t y^-1 and Chalakudy river 101 t y^-1). The discharge of DSi into the Periyar river (40 193 t y^-1) is nearly five times higher than that in the Chalakudy river (8275 t y^-1). The discharges of DFe through the Periyar and Chalakudy rivers are 257 t y^-1 and 36.7 t y^-1, respectively. To sum up, this study addresses the water quality and nutrient flux of two tropical rivers and discusses the impact of urbanization and industrialization on river-water quality.     

Removal of toxic chromium(VI) from aqueous solution by activated carbon using Casuarina equisetifolia

Highly activated carbon from the seed husk of Casuarina Casuarinas equisetifolia, a worldwide famous plant, have been prepared and tested for the removal of toxic Cr(VI) from its aqueous solution. The adsorbent was investigated for influences of initial chromium concentration (75, 100, 125, and 150 mg l^-1), pH, contact time, and quantity of carbon on removal of Cr(VI) from aqueous solution at room temperature (25±2 °C). The adsorption kinetic of Cr(VI) was studied, and the rates of sorption were found to conform to pseudo-second-order kinetics with a good correlation (R²≥0.99). The Langmuir and Freundlich models fit the isotherm data well. Furthermore, the Gibbs free energy was obtained for each system and was found to be-5.29 kJ mol^-1 for removal of Cr(IV). The negative value of Δ G° indicates the feasibility and spontaneous nature of adsorption. The results indicate that acidic pH (1.05) supported the adsorption of Cr(IV) on activated carbon. The maximum adsorption capacity of Cr(VI) on activated carbon was about 172.4 mg g^-1 at pH 1.05.     

Removal of Cr(VI) from aqueous solution using waste weed, Salvinia cucullata

Biosorption studies of Cr(VI) were carried out using waste weed, Salvinia cucullata. Various adsorption parameters were studied, such as agitation speed, contact time, pH, particle size, and concentrations of adsorbent and adsorbate. The equilibrium was achieved in 12 h. A lower pH favoured adsorption of Cr(VI). The kinetics followed pseudo-second-order rate equations. The adsorption isotherm obeyed both the Langmuir and Freundlich models. The calculated activation energy (1.1 kJ mol^-1) suggested that the adsorption followed a diffusion-controlled mechanism. Various thermodynamic parameters such as Δ G^°, Δ H^°, and Δ S^° were also calculated. The positive values of enthalpy indicated the endothermic nature of the reaction, and Δ S^° showed the increasing randomness at the solid liquid interface of Cr(VI) on the adsorbent, which revealed the ease of adsorption reaction. These thermo-dynamic parameters showed the spontaneity of the reaction. The maximum adsorption of uptake (232 mg g^-1) compared well with reported values of similar adsorbents. The rate-determining step was observed to follow an intra-particle diffusion model.     

Toxicity of the nerve agent tabun to Daphnia magna, a new experimental species in military toxicology

Daphnia magna, a freshwater microcrustacean, is currently tested as an alternative experimental species in research dealing with nerve agents poisonings treatment. Because of this, the toxicity of the nerve agent tabun (a cyanide-group containing organophosphate) to Daphnia had to be examined by estimating the EC₅₀ values. The immobilization of daphnids was chosen as the end-point. It was found that D. magna is sensitive to small amounts of tabun, even after 15 min exposure, and tabun toxicity increases with time. The estimated EC₅₀ values for 15, 30, 45, and 60 min exposure were as follows: 67.39, 38.10, 26.95, and 21.9 μg l^-1. In addition, the toxicity of media to which tabun was added 24 h before the start of experiments was examined. The results obtained indicate that daphnids can be used in experiments with nerve-agent intoxication treatment.     

Physicochemical aspects of using natural scavengers in removing methylene blue (basic dye) from solution

Effluent from dyeing and finishing processes is an important source of water pollution. The effectiveness of bentonite, kaolinite and sediment from a local deposit in removing methylene blue as a cationic dye from aqueous solutions has been investigated. The adsorption equilibrium (isotherm) has been determined according to Freundlich and Langmuir equations. The optimum amount is 0.5 g for all adsorbents, and the optimum pH ranges are 2-8 for bentonite and 2-6 for kaolinite and sediment. With respect to kinetic modelling, the adsorption of methylene blue on various adsorbents was fitted to a second-order equation. Also, the thermodynamic parameters were determined. The negative free energy values indicate the feasibility of the process and spontaneous nature of adsorption. The positive ΔH° values indicate the endothermic nature of the process. Thus, Egyptian clay minerals and sediments have a great tendency to remove the dye from solutions.     

Characterization of arsenic content in marine organisms from temperate, tropical, and polar environments

Arsenic is a widely distributed element which occurs in several chemical forms in the marine environment. Inorganic arsenic mediates the most toxic effects and predominates in sea water and sediments, while organisms generally accumulate non-toxic organic forms to concentrations probably reflecting species-specific characteristics in arsenic metabolism. This work represents an additional contribution to our knowledge on natural levels and chemical speciation of arsenic in marine organisms; basal concentrations were characterized in several species (bivalves, crustaceans, and fishes) from different environments (polar, temperate, and tropical latitudes), and results revealed an elevated variability with values ranging from less than 5 to about 200 μg g^-1. No significant effects were observed as a function of the geographical area, with the only exception of crustaceans always showing more elevated arsenic concentrations in Mediterranean species (about 45-110 μg g^-1) compared with tropical species (lower than 30 μg g^-1). Chemical speciation of arsenic was investigated in representative species from the three studied taxa; the predominance of organic forms confirmed the general tendency of marine organisms to bioaccumulate non-toxic arsenic compounds, probably resulting from a detoxification pathway.     

Speciation of organotin compounds in sediments of semi-closed areas along the Mediterranean coast of Alexandria

Organotin compounds were measured in sediments of four different semi-closed areas of the Mediterranean coast of Alexandria: the Eastern Harbour, Western Harbour, El-Max Bay, and Abu-Qir Bay. Due to the commercial trade activity inside the Western Harbour, in addition to the effect of wastes discharged from El Noubaria canal, it shows the highest concentrations of total tin (6.34 μg g^-1 dry weight), dibutyl tin (1.63 μg g^-1 wet weight), tributyl tin (0.33 μg g^-1 wet weight) and diphenyl tin (1.06 μg g^-1 wet weight) compared with other locations. The concentrations of TBT species showed the highest contents compared with DBT and DPhT compounds in all sampling areas. This trend might be due to the worldwide use of TBT not only as biocides in antifouling paints but also as preserving agents for wood, fungicides in agricultural activities, and heat and UV stabilizers of PVC, which results in a direct release of TBT into the water body, accumulation in aquatic fauna. There is also precipitation into sediments and a decrease in degradation rate into its derivatives. Variations, types, concentrations, and distribution of different organotin compounds are discussed in the areas under investigation. The study reveals a new record of organotin compounds along the Alexandria coast and makes comparisons with other surrounding areas of interest.     

Discriminating zooplankton assemblages through multivariate methods: A case for a tropical polluted harbour and Bar-built estuary

A comparative study (June-July 2001) on zooplankton community structure amid polluted conditions in a stagnant harbour and relatively unaffected tidal estuary near Visakhapatnam, on the east coast of India, revealed a marked disparity in species composition and abundance. While the harbour supported a rich population of calanoids (46.4%), the estuary sustained mostly cyclopoids (55.2%). Univariate and multivariate techniques (species diversity, clustering, non-metric multi-dimensional scaling and one-way ANOSIM) revealed the existence of two differing zooplankton assemblages and associated water quality (similarity 50.6%). While the estuary is typified by high amounts of dissolved silica (67.4 ± 17.7 μmol l^-1) linked with monsoon influx, the harbour waters revealed abnormal levels of phosphate (40.9 ± 9.2 μmol l^-1) and nitrate (15.3 ± 5.41 μmol l^{- 1}) suggestive of intense eutrophication, caused by the discharge of fertilizer-factory waste and domestic sewage. On the basis of routines (e.g. BVSTEP, SIMPER) implemented in Plymouth Routines in Multivariate Ecological Research, it was possible to demonstrate that while species such as Oithona rigida, Oithona brevicornis, crustacean nauplii, gastropod veligers, Acartia spinicauda, and Acartia centrura played a key role in discriminating the zooplankton assemblage in the estuary, Acrocalanus spp. (mainly Acrocalanus gracilis) played a keyed role in harbour waters. Canonical Correspondence Analysis revealed species-environment relationships; for example, while the distribution of Oithona spp. and its associates in the estuary corresponded intimately with high silicate, temperature, and low salinity, it was high salinity, phosphate, and nitrate in the harbour channel that supported a different assemblage of copepods dominated by calanoids.     

Integrated biomonitoring assessment of the Lesina Lagoon (Southern Adriatic Coast, Italy): preliminary results

An integrated biomonitoring program for marine and coastal ecosystems quality assessment combines the chemical characterization of a site with the evaluation of the possible structure alterations of its living communities. This can be considered an useful tool for better identifying the summarized effects of all the components interacting with the biota. Such an integrated procedure was carried out for the assessment of the quality of the Lesina Lagoon (Southern Adriatic Coast, Italy). The water parameters levels showed a high primary production (2-6 μg l^-1); the sediment and pore water toxicity bioassays recorded a low or moderate diffused toxicity. Besides, the benthic meiofauna community structure was characterized by prevalent Nematoda taxa with a homogeneous spatial distribution. On these basis, the Lesina Lagoon seems to be characterized by a prevalent organic pollution mainly related to agricultural and zootechnical activities which, due to the lagoon's conformation, presents a homogeneous spatial distribution.     

Heavy-metal distribution and risk assessment of sediment and fish from El-Mex Bay, Alexandria, Egypt

Heavy metals are increasingly being released into natural waters from geological and anthropogenic sources. The distribution of several heavy metals (Cr, Cu, Cd, Pb, Zn, and Hg) was investigated in muscle, gill, and liver in two different fish species seasonally collected in El-Mex Bay (autumn 2004-summer 2005). In order to evaluate the pollution status of the Bay, the concentrations of the selected metals in the labile and total fractions were analysed in sediment samples collected from eight sites in El-Mex Bay during autumn 2004. Also, the Index of Geoaccumulation (I_geo) for the sediment was estimated. The total and labile fractions of the selected metals in sediment samples were 15.2 and 62.8 μg g^-1 dw for Cu, 1.8 and 5.0 μg g^-1 dw for Cd, 79.1 and 130.3 μg g^-1 dw for Zn, 0.2 and 1.2 μg g^-1 dw for Hg, 35.8 and 93.0 μg g^-1 dw for Pb, and 13.9 and 31.0 μg g^-1 dw for Cr. The concentrations of all metals were lower in flesh than those recorded in liver and gill due to their physiological roles. The metal pollution index for fish was calculated. Health hazard calculations for the contaminated sediments and fish consumption were calculated to evaluate the effect of pollution on health.     

Retention of 137cesium in acid sulphate soils of South Central Thailand

Adsorption and desorption of ¹³⁷Cs by acid sulphate soils from the Nakhon Nayok province, South Central Plain of Thailand located near the Ongkarak Nuclear Research Center (ONRC) were investigated using a batch equilibration technique. The influence of added limestone (12 and 18 tons ha^-1) on ¹³⁷Cs adsorption-desorption was studied. Based on Freundlich isotherms, both adsorption and desorption of ¹³⁷Cs were nonlinear. A large portion (98.26-99.97%) of added ¹³⁷Cs (3.7 × 10³-7.03 × 10⁵ Bq l^-1) was sorbed by the soils with or without added lime. The higher lime treatments, however, favoured stronger adsorption of ¹³⁷Cs as compared with soil with no lime, which was supported by higher K_ads values. The addition of lime, the cation exchange capacity and pH of the soil increased and hence favoured the stronger adsorption of ¹³⁷Cs. Acid sulphate soils with a high clay content, medium to high organic matter, high CEC, and predominant clay types consisting of a mixture of illite, kaolinite, and montmorillonite were the main soil factors contributing to the high ¹³⁷Cs adsorption capacity. Competing cations such as NH₄⁺, K⁺, Na⁺, Ca²⁺, and Mg²⁺ had little influence on ¹³⁷Cs adsorption as compared with liming, where a significant positive correlation between K_ads and soil pH was observed. The ¹³⁷Cs adsorption-desorption characteristics of the acid sulphate soils studied exhibited a very strong irreversible sorption pattern. Only a small portion (0.09-0.58%) of ¹³⁷Cs adsorbed at the highest added initial ¹³⁷Cs concentration was desorbed by four successive soil extractions. Results clearly demonstrated that Nakhon Nayok province acid sulphate soils have a high ¹³⁷Cs adsorption capacity, which limits the ¹³⁷Cs bioavailability.     

Heavy-metal adsorption by non-living biomass

The adsorption of some heavy metals onto the walls of harvested, washed, and dried non-living biomass cells of different Pseudomonas strains was studied at optimum experimental conditions using a simplified single component system. The Langmuir adsorption model was found to be a suitable approach to describe the system via multi-step processes. Isotherms measured at 30.0°C and pH 5.5 with [M]_total = 10-100 mM for tight, reversible Cr⁶⁺(aq), Ni²⁺(aq), Cu²⁺(aq) and Cd²⁺(aq) binding by the cell walls of the investigated biomass fit the Langmuir model and give the pH-independent stoichiometric site capacities ν_i and equilibrium constants K_i for metal binding at specific biomass sites i = A, B, C, and D. Tight binding sites A, B, and D of the non-living biomass are occupied by Cr^VI, sites A and C by Ni^II, sites A and D by Cd^II, and only site B by Cu^II. It is concluded that ν_i is a stoichiometric parameter that is independent of the magnitude of K_i for binding site i and that the studied heavy metals selectively and tightly bind at different biomass sites.     

Steam activation,characterisation and adsorption studies of activated carbon from maize tassels

In this paper, steam-produced activated carbon (STAC) from maize tassel (MT) was evaluated for its ability to remove basic dye (methylene blue MB) from aqueous solution in a batch adsorption process. The equilibrium experiments were conducted in the range of 50–300 mg/L initial MB concentrations at 30°C, for effect of pH, adsorbent dosage and contact time. The experimental data were analysed by Langmuir, Freundlich and Temkin isotherm models of adsorption. Freundlich adsorption isotherm was found to have highest value of R²(R²=0.97) compared to other models of Langmuir and Temkin having (0.96 and 0.95 respectively). STAC has a high adsorptive capacity for MB dye (200 mg/g) and also showed favourable adsorption for the dye with the separation factor (R_L<1) for the dye-activated carbon system. The kinetic data obtained were analysed using pseudo first-order kinetic equation and pseudo second-order kinetic equation. The experimental data fitted well into pseudo second-order kinetic equation, as demonstrated by the high value of R².     

Contributions of adsorption,bioreduction and desorption to uranium immobilization by extracellular polymeric substances

● EPS immobilizes U(VI) via adsorption, bioreduction and desorption. ● This work provides a framework to quantify the three immobilization processes. ● The non-equilibrium adsorption of U follows pseudo-second-order kinetics. ● The equilibrium adsorption of U followed Langmuir and Freundlich isotherms. Hexavalent uranium (U(VI)) can be immobilized by various microbes. The role of extracellular polymeric substances (EPS) in U(VI) immobilization has not been quantified. This work provides a model framework to quantify the contributions of three processes involved in EPS-mediated U(VI) immobilization: adsorption, bioreduction and desorption. Loosely associated EPS was extracted from a pure bacterial strain, Klebsiella sp. J1, and then exposed to H₂ and O₂ (no bioreduction control) to immobilize U(VI) in batch experiments. U(VI) immobilization was faster when exposed to H₂ than O₂ and stabilized at 94% for H₂ and 85% for O₂, respectively. The non-equilibrium data from the H₂ experiments were best simulated by a kinetic model consisting of pseudo-second-order adsorption (k_a = 2.87 × 10⁻³ g EPS·(mg U)⁻¹·min⁻¹), first-order bioreduction (k_b = 0.112 min⁻¹) and first-order desorption (k_d = 7.00 × 10⁻³ min⁻¹) and fitted the experimental data with R² of 0.999. While adsorption was dominant in the first minute of the experiments with H₂, bioreduction was dominant from the second minute to the 50^th min. After 50 min, adsorption was negligible, and bioreduction was balanced by desorption. This work also provides the first set of equilibrium data for U(VI) adsorption by EPS alone. The equilibrium experiments with O₂ were well simulated by both the Langmuir isotherm and the Freundlich isotherm, suggesting multiple mechanisms involved in the interactions between U(VI) and EPS. The thermodynamic study indicated that the adsorption of U(VI) onto EPS was endothermic, spontaneous and favorable at higher temperatures.     

Equilibrium studies on the adsorption of acid dye into chitin

We report the adsorption isotherm of acid dye on the surface of chitin, a unique solid adsorbent. Adsorption process offers an attractive benefit for a dyeing house treatment. Influences of essential kinetic parameters such as adsorbent particle size, reaction temperature governing the dye adsorption have been investigated. Adsorptions isotherms of dye on chitin were developed and the equilibrium data fitted well to the Langmuir, Freundlich and Redlich Peterson isotherm model. At optimum conditions maximum dye adsorption capacity of chitin estimated with the Langmuir 44.0, 85.0, 104.3 mg/g and 85.0, 114.10, 113.62 mg/g adsorbent. The results showed that chelating polymer of chitin could be considered as potential adsorbents for acid dye removal from dilute solution.     

Magnetic particles precipitated onto wheat husk for removal of methyl blue from aqueous solution

Magnetic particles prepared via co-precipitation and impregnated onto wheat husk (MN-WH) were used for the removal of methyl blue (MB) from aqueous solution. Experiments were conducted in a batch mode for optimization regarding pH, contact time, adsorbent dose, initial dye concentrations, and temperature. Maximum adsorption (98%) was achieved at pH 5. The adsorption data were fitted into pseudo-first, pseudo-second, intraparticle diffusion, and Elovich equation revealing that adsorption followed pseudo-second-order kinetics. The four most common isotherm models, i.e. the Langmuir, Freundlich, Tempkin, and Dubinin–Radushkevich (D–R), were used to evaluate the data, with the best fit to a Langmuir isotherm (R² = 0.996), followed by a Freundlich isotherm (R² = 0.995), indicating monolayer adsorption of MB on the surface of MN-WH. Thermodynamic parameters calculated from the Van't Hoff equation revealed that the adsorption is exothermic (ΔHº = ?19.7 kJ mol^?1).