A biofilm reactor was designed with flat ceramic substrates to remove Co(II), Ni(II) and Zn(II) from industrial wastewater. The ceramics were made of clay and nano-rubber with high mechanical resistance. The surface of the ceramic substrate was modified with neutral fiber and nano-hydroxyapatite. A uniform and stable biofilm mass of 320 g with 2 mm of thickness was produced on the modified ceramic after 3 d. The micro-organisms were identified in the biofilm by polymerase chain reaction (PCR) method. Functional groups of biofilms were identified with a Fourier transform infrared spectrometer (FT-IR). Experiments were designed by central composite design (CCD) using the responsive surface method (RSM). The biosorption process was optimized at pH = 5.8, temperature = 22 °C, feed flux of heavy metal wastewater = 225 ml, substrate flow = 30 ml, and retention time = 7.825 h. The kinetic data was analyzed by pseudo first-order and pseudo second-order kinetic models. Isotherm models and thermodynamic parameters were applied to describe the biosorption equilibrium data of the metal ions on the biofilm-ceramic. The maximum biosorption efficiency and capacity of heavy metal ions were about 72% and 57.21 mg, respectively.

In the present investigation seaweeds of macroalgae like Kappaphycus alvarezii, Gracilaria salicornia and Gracilaria edulis used as novel biosorbent in native (KA, GS, GE) and ethanol modified (EKA, EGS, EGE) for Rhodamine B (RB) removal from aqueous solution in batch process. Effect of various biosorption parameters such as pH, initial concentration of RB, biosorbent dosage and contact time were studied. The maximum biosorption capacity determined as 9.84 (KA), 11.03 (GS), 8.96 (GE), 112.35 (EKA), 105.26 (EGS) and 97.08 mg/g (EGE), respectively towards the removal of RB from aqueous solutions. Better removal of RB was observed using EKA, EGS, and EGE biosorbents at 2.0 pH. The characterizations of the biosorbents were performed using Scanning Electron microscope and Fourier Transform Infrared Spectroscopy. Biosorption equilibrium data evaluated using Langmuir, Freundlich, Temkin, Dubinin-Radushkevich and Jovanovic isotherm model. The Langmuir isotherm model best suited the equilibrium data for all the biosorbents studied. The rate of RB removal subjected to kinetic analysis using pseudo-first-order, pseudo-second-order, intra-particle diffusion and Elovich models. Pseudo-second-order kinetic model better described the experimental data of the RB biosorption. Desorption studies performed using 0.1 M sodium hydroxide as eluting agents for regeneration and recycle analysis. The recyclability of the six biosorbents showed consistent biosorption capacity towards RB removal up to the entire three cycles. The studied biosorbents sourced from large volume and easily available, further biosorption performance indicated that the KA, GS, GE, EKA, EGS and EGE could be used as efficient, alternative and eco-friendly biosorbents for the removal of harmful dyes in the environment.

Metal-resistant bacteria can survive exposure to high metal concentrations without any negative impact on their growth. Biosorption is considered to be one of the more effective detoxification mechanisms acting in most bacteria. However, molecular-scale characterization of metal biosorption by wild metal-resistant bacteria has been limited. In this study, the Pb(II) biosorption behavior of Serratia Se1998 isolated from Pb-contaminated soil was investigated through macroscopic and microscopic techniques. A four discrete site non-electrostatic model fit the potentiometric titration data best, suggesting a distribution of phosphodiester, carboxyl, phosphoryl, and amino or hydroxyl groups on the cell surface. The presence of these functional groups was verified by the attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, which also indicated that carboxyl and phosphoryl sites participated in Pb(II) binding simultaneously. The negative enthalpy (−9.11 kJ mol−1) and large positive entropy (81.52 J mol−1 K−1) of Pb(II) binding with the bacteria suggested the formation of inner-sphere complexes by an exothermic process. X-ray absorption fine structure (XAFS) analysis further indicated monodentate inner-sphere binding of Pb(II) through formation of C−O−Pb and P−O−Pb bonds. We inferred that C−O−Pb bonds formed on the flagellar surfaces, establishing a self-protective barrier against exterior metal stressors. This study has important implications for an improved understanding of metal-resistance mechanisms in wild bacteria and provides guidance for the construction of genetically engineered bacteria for remediation purposes.

Phycoremediation technologies significantly contribute to solving serious problems induced by heavy metals accumulation in the aquatic systems. Here we studied the mechanisms underlying Al stress tolerance in two diazotrophic cyanobacterial species, to identify suitable species for Al phycoremediation. Al uptake as well as the physiological and biochemical responses of Anabaena laxa and Nostoc muscorum to 7 days Al exposure at two different concentrations i.e., mild (100 μM) and high dose (200 μM), were investigated. Our results revealed that A. laxa accumulated more Al, and it could acclimatize to long-term exposure of Al stress. Al induced a dose-dependent decrease in photosynthesis and its related parameters e.g., chlorophyll content (Chl a), phosphoenolpyruvate carboxylase (PEPC) and Ribulose‒1,5‒bisphosphate carboxylase/oxygenase (RuBisCo) activities. The affect was less pronounced in A. laxa than N. muscorum. Moreover, Al stress significantly increased cellular membrane damage as indicated by induced H₂O₂, lipid peroxidation, protein oxidation, and NADPH oxidase activity. However, these increases were lower in A. laxa compared to N. muscorum. To mitigate the impact of Al stress, A. laxa induced its antioxidant defense system by increasing polyphenols, flavonoids, tocopherols and glutathione levels as well as peroxidase (POX), catalase (CAT), glutathione reductase (GR) and glutathione peroxidase (GPX) enzymes activities. On the other hand, the antioxidant increases in N. muscorum were only limited to ascorbate (ASC) cycle. Overall, high biosorption/uptake capacity and efficient antioxidant defense system of A. laxa recommend its feasibility in the treatment of Al contaminated waters/soils.

The level of radioactivity in the soil has been increasing unpredictably due to the human uranium mining exploitation of uranium over the past 100 years. Remediation of metals in actual soil confronts many challenges, remaining poorly understood. This study intends to investigate the concentrations and distributions of U, Cd, Zn, Pb, and Cu in soils surrounded by a uranium mill tailing pond. Furthermore, a phosphorus-modified bio-char was prepared in order to determine its role in immobilizing uranium in soil samples. Results show that the contents of U and Pb are much higher than that of the background values, due to the influence of the uranium mill tailing pond. Phosphorus can enhance the immobilization efficiency of U, Cd, Pb, and Cu in soil samples. The concentration of uranium in the leaching supernatant of phosphorus-modified bio-char group is lower than that of control and unmodified bio-char groups due to the fact that the biosorption occurred in the exterior surface of the biomass, which imply that phosphorus-modified bio-char is a potential immobilization material to reduce the leaching rate of metals. These findings can provide references for remediation technology of metals in natural soil.

It was investigated the potential of Rhodococcus erythropolis AW3 as a biosorbent for the removal of crystal violet (CV) dye from natural water and real effluents. The biosorbent was characterized by flow cytometry, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy X-ray dispersive spectroscopy (EDS), and point of zero charge (pHZPC). Batch biosorption experiments were performed to optimize different parameters involved in the biosorption process. The equilibrium was reached at 90 min at the optimum biosorbent dose of 0.50 g L⁻¹ and pH of 9.0. Results indicated that Langmuir isotherm model was the most suitable to represent the experimental data, and the highest biosorption capacity was 289.8 mg g⁻¹. Kinetic data were well fitted with the pseudo-second-order model. The thermodynamic study showed that the process was favorable, exothermic, and associated with an increase of entropy. Finally, it was demonstrated that the biosorption process using Rhodococcus erythropolis AW3 could be successfully applied to remove CV from natural water and effluents derived from clinical and industrial activities.

Biological materials play a significant role in the treatment of heavy metal-contaminated soil and wastewater. In this study, the Pb²⁺ biosorption potential of lichen Evernia prunastri, extensively available at a forest in Bilecik-Turkey, was investigated at batch-scale level. The optimal conditions were determined and the adsorption isotherms, kinetics, and thermodynamic calculations were also done. In order to have detailed knowledge about metal biosorption, SEM, FTIR, and BET analyses were carried out before and after the biosorption process. The optimal pH was found pH 4 and the maximum metal uptake capacity was found as 0.067 mol kg⁻¹. The results of this study indicate that the lichen was effectively applied to the removal of Pb²⁺ process as an inexpensive biosorbent from industrial wastewater.

Combustion of fossil fuels including coal is one of the sources of mercury pollution. Combustion waste from fly ash disposal sites poses a problem for the environment and constitutes a potential source of Hg, thus phytostabilisation is a crucial goal in the mitigation of fossil fuel impact. The paper presents mercury (Hg) concentration in technosols from combustion waste and in individual biomass components (fine roots, bark, stem wood and leaves) of alder species (black, gray and green alder) introduced as part of a long-term experiment to develop a method of phytostabilisation and afforestation of a lignite combustion disposal site. Mercury content in the combustion waste was elevated compared to the data for natural soils from uncontaminated forest areas, however, it did not exceed the amounts considered to be toxic. Hg content in technosols was related to clay and silt fraction content and phosphorus content. Mercury in the alder biomass accumulated mainly in the underground part, especially in the fine roots and displayed a positive correlation with acid and alkaline phosphatase and sulfur content, with no differences in the accumulation of Hg between the alder species. The obtained results indicate that the fine roots are the frontier of Hg biosorption in developed alder systems on combustion waste disposal sites.

The immobilized algae Sargassum vulgare was used as biosorbent for Fe³⁺ removal through a batch and continuous system in order to study the biosorption capacity and to establish a new method of the valorization of this waste. The kinetic data could be described by the pseudo first-order and pseudo second-order kinetic models. The batch equilibrium was fitted by the Langmuir model with a value of correlation coefficient (R² = 0.98) higher than that of the Freundlich (R² = 0.89). The process was exothermic and spontaneous and the biomass was successfully desorbed using 0.1 M HCl. Furthermore, the Thomas model, Bohart-Adams model, and Yoon-Nelson model were successfully applied to evaluate the dynamic behavior of Fe³⁺ biosorption in a fixed-bed column. The lower flow rate of 1.04 ml/min showed the greater performance of the process. Fourier transform infrared spectroscopy revealed the presence of several active binding sites, and scanning electron microscopy micrograph confirmed the metal adsorption on the surface. The results reveal that the immobilized algae have a potential removal for Fe³⁺ in a batch and continuous system.

With increasing concern related to sustainable chemistry, we investigated the biosorption of Pb²⁺ ions from aqueous medium using an environmental friendly and economic biosorbent Bougainvillea spectabilis (BS). The BS was modified effectively using citric acid by hydrothermal method. The biosorbent(s) was characterized by scanning electron microscope (SEM), energy dispersion X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA), and point of zero charge (pHₚzc). Various process parameters including biosorbent dosage, time of contact, temperature, solution pH, and initial Pb²⁺ ions concentration were studied in batch mode. Kinetic modeling was performed to evaluate the kinetic data and results showed that the studied process followed the pseudo second order (PSO) kinetics. Equilibrium modeling was done using famous equilibrium models, i.e., Langmuir, Freundlich, Dubinin-Kaganer-Radushkevish, and Temkin in non-linear fashion to evaluate equilibrium data by varying initial Pb²⁺ ions concentration from 20 to 180 mg/L. Based on RMSE values, Langmuir model fits best. This paper also discusses thermodynamic parameters (i.e., enthalpy, entropy, and free energy) showing that the process was spontaneous and endothermic in nature. In comparison with BS (B. spectabilis), an appreciable increase in uptake capacity of CABS (citric acid modified B. spectabilis) was observed in sequestration of Pb²⁺ ions from aqueous medium showing advantage of citric acid modification making it industrially favorable and socially acceptable biosorbent for efficient removal of lead from water.