Reliable sustainable management strategies for flare gas recovery: technical, environmental, modeling, and economic assessment: a comprehensive review.

The gas flaring network is an inseparable constituent commonly present in most of the oil and gas refineries and petrochemical facilities conferring reliable operational parameters. The improper disposal of burn-off gases improperly results in environmental problems and loss of economic resources. In this regard, waste to energy transforming nexus, in accord with the "carbon neutrality" term, has potentially emerged as a reasonable pathway to preserve our planet. In a transdisciplinary manner, the present review article deeply outlines the different up-to-date strategies developed to recover the emitted gases (flaring minimization) into different value-added products. To analyze the recovery potential of flare gases, different technologies, and decision-making factors have been critically reviewed to find the best recovery methods. We recommend more straightforward recovery methods despite lower profits. In this regard, electricity generation seems to be an appropriate option for application in small amounts of flaring. However, several flare gas utilization processes such as syngas manufacturing, reinjection of gas into petroleum reservoirs, and production of natural gas liquid (NGL) are also recommended as options because of their economic significance, technological viability (both onshore and offshore), and environmental benefits. Moreover, the adopted computational multi-scale data assimilation for predictive modeling of flare gas recovery scenarios has been systematically reviewed, summarized, and inspected.

Dual valorization of coastal biowastes for tetracycline remediation and biomethane production: A composite assisted anaerobic digestion.

Harnessing coastal biowaste for dual valorization in water treatment and biofuel production holds paramount importance for sustainability and resource challenges. This study investigated the potential of engineered composite (CABC) derived from coastal biowaste-based materials for tetracycline (TC) removal and biomethane production. High-yield calcium carbonate (CaCO3; 95.65%; bivalve shells) and biochar (GA-BC; 41.50%; green macroalgae) were produced and used as precursors for CABC. The characterization results revealed presence of ß-CaCO3 and ν2-CO3 aragonite in CaCO3, and composite homogeneity was achieved. The CABC exhibited a maximum TC sorption capacity of 342.26 mg/g via synergistic sorption mechanisms (i.e., surface/pore filling, electrostatic attraction, calcium ion exchange, and chelation). Supplementation of anaerobic digestion process with GA-BC, CaCO3, and CABC was investigated via three consecutive cycles. Biochemical methane potential of glucose as a sole substrate was increased from 157.50 to 217.00, 187.00, and 259.00 mL-CH4, while dual substrate (glucose+TC) treatment was increased from 94.5 to 146.5, 129.0, and 153.00 mL-CH4 for GA-BC, CaCO3, and CABC, respectively. Moreover, system stability and TC removal were increased with the addition of GA-BC (40.90%), CaCO3 (16.30%), and CABC (53.70%). Therefore, this study exemplifies the circular bioeconomy approach, demonstrating the sustainable use of biowaste-derived composite for water treatment and biofuel production.

Cationic Surfactant-Modified Tetraselmis sp. for the Removal of Organic Dyes from Aqueous Solution.

The modification of the Tetraselmis sp. algae material (Tetra-Alg) with surfactant Cethyltrimethylammonium Bromide (CTAB) yielded adsorbent Tetra-Alg-CTAB as an adsorbent of methyl orange (MO) and methylene blue (MB) solutions. The characterization of the adsorbent used an infrared (IR) spectrometer to identify functional groups and Scanning Electron Microscopy with Energy Dispersive X-ray (SEM-EDX FEI Inspect-S50, Midland, ON, Canada) to determine the surface morphology and elemental composition. Methyl orange and methylene blue adsorption on the adsorbent Tetra-Alg, Tetraselmis sp. algae-modified Na+ ions (Tetra-Alg-Na), and Tetra-Alg-CTAB were studied, including variations in pH, contact time, concentration, and reuse of adsorbents. The adsorption of MO and MB by Tetra-Alg-CTAB at pH 10, during a contact time of 90 min, and at a concentration of 250 mg L-1 resulted in MO and MB being absorbed in the amounts of 128.369 and 51.013 mg g-1, respectively. The adsorption kinetics and adsorption isotherms of MO and MB and Tetra-Alg, Tetra-Alg-Na, and Tetra-Alg-CTAB tend to follow pseudo-second-order kinetics models and Freundlich adsorption isotherms with each correlation coefficient value (R2) approaching 1. Due to the modification with the cationic surfactant CTAB, anionic dyes can be strongly sorbed in alkaline pH due to strong electrostatic attraction, while MB is more likely to involve cation exchange and hydrogen bonding. The reuse of Tetra-Alg-CTAB was carried out four times with adsorption percent > 70%, and the adsorbent was very effective in the adsorption of anionic dyes such as MO.

Effect of the magnetic core in alginate/gum composite on adsorption of divalent copper, cadmium, and lead ions in the aqueous system.

The change of composition of an adsorbent material has been widely used as a method to increase its adsorption capacity, particularly concerning adsorbents made of polysaccharides. Introducing magnetic adsorbents into contaminated water treatment systems is a highly promising strategy, as it promotes the metal ions removal from water. Considering this, gum Arabic (GA) was associated with alginate (Alg), when magnetite nanoparticles were present or absent, to produce beads that were utilised to take up Cu(II), Cd(II), and Pb(II) from aqueous solution. After a complete characterisation (for which Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, and swelling were used), the adsorption properties were established using batch and column tests. The magnetic beads (MAlg/GA) demonstrated improved adsorption in comparison with the beads made without magnetite (Alg/GA) under the same conditions. In normal adsorption conditions (pH 6.0, 25 °C, 2.5 g L-1 of adsorbent dosage), the highest uptake capacities recorded for the MAlg/GA beads were: for Cu(II), 1.33 mmol g-1; Cd(II), 1.59 mmol g-1; and for Pb(II), 1.43 mmol g-1. The pseudo-second-order kinetics and Langmuir isotherm models provided good fits for the adsorption of these metals. Overall, ion exchange and physical forces led to the uptake of these metals by both Alg/GA and MAlg/GA; moreover, the functional groups on the beads played crucial roles as binding sites. Additionally, it was observed that flow rates of >2 mL min-1 did not produce noticeable changes in uptake levels over the same flow period. It was found that the efficient eluting agent was HNO3 (0.2 M). In some cases, the metals were not removed fully from the used beads during the first five cycles of regeneration and reuse. The results of this investigation show that these beads are efficient adsorbents for the removal of metal ions from spiked well water samples.

Functionalization of carbon from rubber fruit shells (Hevea brasiliensis) with silane agents and its application to the adsorption of bi-component mixtures of methylene blue and crystal violet.

In this research, activated carbon was obtained from rubber fruit shells (ACRPs). The obtained activated carbon (ACRPs) was modified by magnetite particle coating and silanization with triethoxyiphenylsilane (TEPS) to produce a new magnetic adsorbent (ACRPs-MS). The affinity of as-prepared adsorbent (ACRPs-MS) toward methylene blue (MB) and crystal violet (CV) dyes was tested in mono-component and bi-component solutions. Structural characterization proves the success of the magnetite coating process and the silanization of ACRPs. In the infrared (IR) spectroscopy spectrum of ACRPs-MS, Si-O-Fe and Si-O-Si bonds were identified, which indicated the presence of magnetite and silane. This is also supported by the elemental composition contained in the energy-dispersive X-ray (EDX) diffractogram. In addition, the presence of the porous structure of the surface of the material and the increase in the specific surface area increase the accessibility of contaminants such as MB and CV dyes to be adsorbed to the ACRPs-MS adsorption site effectively. The experimental results showed that the adsorption of mono-component MB and CV dyes by ACRPs-MS was optimum at pH 8 and an interaction time of 60 min. The adsorption kinetics of mono-component MB and CV dyes by ACRPs-MS tended to follow pseudo-second-order kinetics (PSO) models with PSO rate constant (k2) values of 0.198 and 0.993 g mg-1 min-1, respectively. The adsorption of MB and CV dyes by ACRPs-MS in a bi-component mixture tends to follow the Langmuir isotherm model with adsorption capacity (qm) values of 85.060 and 90.504 mg g-1, respectively. Analysis of adsorption data on the bi-component mixture between MB and CV by ACRPs-MS with the Langmuir isotherm equation for a binary mixture resulted in qm of 22.645 × 10-3 mmol equiv g-1. ACRPs-MS material can be used repeatedly five times with adsorption ability > 80%. Desorption of MB and CV dyes was carried out using 0.05 M HCl solution. ACRPs-MS material was able to adsorb MB and CV dyes with a large adsorption capacity and could be used in repeated adsorption. Thus, it can be stated that ACRPs-MS can be used as an effective adsorbent for MB and CV dyes, either singly or in a bi-component mixture.

Sustainable management of food waste; pre-treatment strategies, techno-economic assessment, bibliometric analysis, and potential utilizations: A systematic review.

Food waste (FW) contains many nutritional components such as proteins, lipids, fats, polysaccharides, carbohydrates, and metal ions, which can be reused in some processes to produce value-added products. Furthermore, FW can be converted into biogas, biohydrogen, and biodiesel, and this type of green energy can be used as an alternative to nonrenewable fuel and reduce reliance on fossil fuel sources. It has been demonstrated in many reports that at the laboratory scale production of biochemicals using FW is as good as pure carbon sources. The goal of this paper is to review approaches used globally to promote turning FW into useable products and green energy. In this context, the present review article highlights deeply in a transdisciplinary manner the sources, types, impacts, characteristics, pre-treatment strategies, and potential management of FW into value-added products. We find that FW could be upcycled into different valuable products such as eco-friendly green fuels, organic acids, bioplastics, enzymes, fertilizers, char, and single-cell protein, after the suitable pre-treatment method. The results confirmed the technical feasibility of all the reviewed transformation processes of FW. Furthermore, life cycle and techno-economic assessment studies regarding the socio-economic, environmental, and engineering aspects of FW management are discussed. The reviewed articles showed that energy recovery from FW in various forms is economically feasible.

Methylene blue removal from aqueous solutions using a biochar/gellan gum hydrogel composite: Effect of agitation mode on sorption kinetics.

Hydrogel membranes are prepared by casting a mixture of gellan gum (associated with PVA) and biochar produced from a local Egyptian plant. The mesoporous material is characterized by a specific surface area close to 134 m2 g-1, a residue of 28 % (at 800 °C), and a pHPZC close to 6.43. After grinding, the material is tested for Methylene Blue sorption at pH 10.5: sorption capacity reaches 1.70 mmol MB g-1 (synergistic effect of the precursors). The sorption isotherms are fitted by both Langmuir and Sips eqs. MB sorption increases with temperature: the sorption is endothermic (∆H°: 12.9 kJ mol-1), with positive entropy (∆S°: 125 J mol-1 K-1). Uptake kinetics are controlled by agitation speed (optimum ≈200 rpm) and resistance to intraparticle diffusion. The profiles are strongly affected by the mode of agitation: the equilibrium time (≈180 min) is reduced to 20-30 min under sonication (especially at frequency: 80 kHz). The mode of agitation controls the best fitting equation: pseudo-first order rate agitation for mechanical agitation contrary to pseudo-second order rate under sonication. The sorption of MB is poorly affected by ionic strength (loss <6 % in 45 g L-1 NaCl solution). Desorption (faster than sorption) is completely achieved using 0.7 M HCl solution. At the sixth recycling, the loss in sorption is close to 5 % (≈ decrease in desorption efficiency). The process is successfully applied for the treatment of MB-spiked industrial solution: the color index decreases by >97 % with a sorbent dose close to 1 g L-1; a higher dose is required for maximum reduction of the COD (60 % at 3 g L-1).

Tuning cationic/anionic dyes sorption from aqueous solution onto green algal biomass for biohydrogen production.

Global water security and energy demands associated with uncontrollable population growth and rapid industrial progress are one of the utmost serious needs dangerously confronting humanity. On account of waste as a wealth strategy; a multifunctional eco-friendly sorbent (MGAP) from green alga was prepared successfully for remediation of cationic/anionic organic dyes and biohydrogen production. The structural and morphological properties of sorbent were systematically scrutinized by a variety of spectral analyses. The loading capacity of MGAP towards rhodamine B (RhB) and methyl orange (MO) dyes was inclusivity inspected under variable experimental conditions. The adsorption kinetics of both dyes onto MGAP was in good agreement with pseudo-second-order theory, whereas adsorption isotherms could fit well with the Langmuir model, with satisfactory loading capacities of 144.92 and 196.04 mg g-1 for RhB and MO molecules, respectively. Moreover, ultra-sonication treatment admirably decreased the sorption equilibrium time from 180.0 min to 30.0 min. Furthermore, spent sorbent was managed particularly for biohydrogen production with a measured yield of 112.89, 116.59, and 128.17 mL-H2/gVS for MGAP, MGAP-MO, and MGAP-RhB, respectively. Overall, the produced MGAP can potentially be offered up as a promising dye scavenger for wastewater remediation and biohydrogen production, thereby fulfilling waste management and circular economy.

Biosorption kinetics of cerium(III) and cobalt(II) from liquid wastes using individual bacterial species isolated from low-level liquid radioactive wastes.

The existence of toxic heavy metals in the aquatic environment has emphasized a considerable exigency to develop several multifunctional biosorbents for their removal. Herein, three individual bacterial species of Cellulosimicrobium cellulans, Bacillus coagulans, and Microbacterium testaceum were successfully isolated from low-level liquid radioactive wastes. Their loading capacities towards cerium and cobalt metal ions were inclusivity inspected under variable operational parameters of pH, primary pollutant concentration, interaction time, temperature, stirring speed, and biosorbent dosage. By analyzing the influence of solution pH, concentration, temperature, biosorbent mass, and agitation speed on the biosorption kinetics, the biosorption process confirms pseudo-second-order kinetic, intraparticle diffusion, and Elovich equation. Remarkably, the isolated Microbacterium testaceum exhibited high loading capacities reaching 68.1 mg g-1, and 49.6 mg g-1 towards Ce(III), and Co(II) ions, respectively, at the initial concentration of 2.8 mM, pH 4.5, and 25 °C. Overall, the isolated bacterial species can potentially be offered up as a promising scavenger for Ce(III) and Co(II) from liquid waste effluents.

U(VI) and Th(IV) recovery using silica beads functionalized with urea- or thiourea-based polymers - Application to ore leachate.

Urea and thiourea have been successfully deposited at the surface of silica beads (through one-pot reaction with formaldehyde) for designing new sorbents for U(VI) and Th(IV) recovery (UR/SiO2 and TUR/SiO2 composites, respectively). These materials have been characterized by FTIR, titration, elemental analysis, BET, TGA, SEM-EDX for identification of structural and chemical properties, and interpretation of binding mechanisms. Based on deprotonation of reactive groups (amine, carbonyl, or thiocarbonyl) and metal speciation, the optimum pH was ~4. Uptake kinetics was fast (equilibrium within 60-90 min). Although the kinetic profiles are fitted by the pseudo-first order rate equation, the resistance to intraparticle diffusion cannot be neglected. Sorption isotherms were fitted by Langmuir equation (maximum sorption capacities: 1-1.2 mmol g-1). Thermodynamics are also investigated showing differences between the two types of functionalized groups: exothermic for TUR/SiO2 and endothermic for UR/SiO2. Metal desorption is highly effective using 0.3-0.5 M HCl solutions: total desorption occurs within 30-60 min; sorption/desorption properties are remarkably stable for at least 5 cycles. The sorbents have marked preference for U(VI) and Th(IV) over alkali-earth and base metals at pHeq ~4.8. By preliminary precipitation steps, it is possible "cleaning" ore leachates of pegmatite ore, and recovering U(VI) and Th(IV) using functionalized silica beads. After elution and selective recovery by precipitation with oxalate (Th-cake) and alkaline (U-cake), the metals can be valorized.

Phosphorylation of Guar Gum/Magnetite/Chitosan Nanocomposites for Uranium (VI) Sorption and Antibacterial Applications.

The development of new materials is needed to address the environmental challenges of wastewater treatment. The phosphorylation of guar gum combined with its association to chitosan allows preparing an efficient sorbent for the removal of U(VI) from slightly acidic solutions. The incorporation of magnetite nanoparticles enhances solid/liquid. Functional groups are characterized by FTIR spectroscopy while textural properties are qualified by N2 adsorption. The optimum pH is close to 4 (deprotonation of amine and phosphonate groups). Uptake kinetics are fast (60 min of contact), fitted by a pseudo-first order rate equation. Maximum sorption capacities are close to 1.28 and 1.16 mmol U g-1 (non-magnetic and magnetic, respectively), while the sorption isotherms are fitted by Langmuir equation. Uranyl desorption (using 0.2 M HCl solutions) is achieved within 20-30 min; the sorbents can be recycled for at least five cycles (5-6% loss in sorption performance, complete desorption). In multi-component solutions, the sorbents show marked preference for U(VI) and Nd(III) over alkali-earth metals and Si(IV). The zone of exclusion method shows that magnetic sorbent has antibacterial effects against both Gram+ and Gram- bacteria, contrary to non-magnetic material (only Gram+ bacteria). The magnetic composite is highly promising as antimicrobial support and for recovery of valuable metals.

Correction to: Role of identified bacterial consortium in treatment of Quhafa wastewater treatment plant influent in Fayuom, Egypt.

The original version of this article unfortunately contained an error.

The synergistic effect of ultrasound power and magnetite incorporation on the sorption/desorption behavior of Cr(VI) and As(V) oxoanions in an aqueous system.

Though abundant studies have targeted the sorption of Cr(VI) and As(V) anions by organic polymers or magnetic metal oxides, there is no research literature on the sorption characteristics of Cr(VI) and As(V) by thiourea-formaldehyde resin (TF) and its magnetic derivative (MTF). TF resin is a strong chelating agent, which has several practical applications. This paper reports on the removal of Cr(VI) and As(V) oxoanions by TF and MTF sorbents. The sorbents were characterized by Fourier transform infrared (FTIR), nuclear magnetic resonance (NMR) spectroscopy, elemental analysis, zetametry, Brunauer-Emmett-Teller (BET) analysis, and differential light scattering (DLS). The synergistic influence of magnetite incorporation and ultrasonic power on sorption kinetics, isotherms, and oxoanion desorption were investigated, including the analysis of the uncertainty in the study results. The relationship between kinetic and equilibrium constants of the two sorbents under normal shaking and ultrasound shaking was analysed. Ultrasound power improved the mass transfer and makes the sorption ultra-fast while magnetite enhanced the sorption capacity. The MTF particles sorbed 4.28 and 1.97 mmol g-1 of Cr(VI) and As(V), respectively, under optimum conditions. Further, desorption kinetics and efficiency of Cr(VI) and As(V) were estimated using normal shaking and ultrasonic agitation. Ultrasound power reduced the time and the concentration of NaCl required for the stabilization of desorption efficiency.

Role of identified bacterial consortium in treatment of Quhafa Wastewater Treatment Plant influent in Fayuom, Egypt.

This study was aimed to biologically treat domestic wastewater using identified bacterial consortium for chemical pollutants removal by treating/passing it through sand biofilters. The identification, toxicity test, and the optimum dose of the investigated bacterial consortium were carried out using Microtox analyzer and Batch biological treatment, respectively. Furthermore, application of sedimentation followed by gravel and sand biofilters for wastewater treatment was evaluated. The results showed that the bacterial consortium is composed of Pediococcus acidilactici, Pediococcus pentosaceus, Lactobacillus plantarum, and Bacillus subtilis. The optimum dose for wastewater treatment within 6 h of contact time is 2.5 mg/L, this dose (2.5 mg/L) has no toxic effect. The removal percentage of chemical oxygen demand (COD), biological oxygen demand (BOD), total solids (TS), total dissolved solids (TDS), total suspended solids (TSS), ammonia, nitrate, total Kjeldahl nitrogen (TKN), and oil and grease reached 93.4, 83.5, 37.5, 49.2, 93.4, 100, 55.7, 76.6, and 76% in the effluent of the treated wastewater, respectively after the third sand biofilter filtration. It can be concluded that using bacterial consortium for domestic wastewater treatment could be a good tool for chemical pollutants removal. Moreover, this study provides low cost and eco-friendly tool for domestic wastewater treatment using simple multistage biofilters based on an identified bacterial consortium. This system can be upscaled for the treatment of larger volumes of wastewater.

Microwave-accelerated sorption of cationic dyes onto green marine algal biomass.

Monolithic algal green powder (MAGP) was fabricated based on the marine green macroalga Enteromorpha flexuosa. It was scrutinized by using scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), Fourier transform infrared (FT-IR), point of zero charge (PHPZC), and Brunauer-Emmett-Teller (BET) surface area. The ability of Enteromorpha flexuosa to capture both crystal violet (CV) and methylene blue (MB) from aqueous solutions was evaluated. The influence of variable conditional parameters on CV dye and MB dye batch sorption was investigated. Results showed that percentage removal of 90.3% and 93.4% were obtained under optimum conditions of variables for CV and MB, respectively. Effect of microwave radiation on dye sorption was also appraised. Processing the sorption under microwave irradiation (microwave-enforced sorption, MES) increases mass transfer and a contact time as low as 1 min is sufficient under optimized conditions (exposure time and power) reaching the equilibrium. The reusability of MAGP sorbent was achieved for four cycles of sorption/desorption by using 0.5 M HCl. The ability of MAGP for cationic dyes removal from spiked tap water and petrochemical plant discharge wastewater samples was successfully registered. Ultimately, the displayed data showed a superior and excellent ability of algal powder to be exploited as a green, harmless, and effective sorbent for cationic dye removal.

Investigation of novel nanomaterial for the removal of toxic substances from contaminated water.

Ligand-functionalized nanomaterials exhibit great potential for the removal of hazardous substances from the environment and industrial wastewater. In this work, a composite nanosphere material was fabricated using mesoporous silica and organic ligand, and employed for the efficient detection and subsequent removal of toxic sulfanilamide (SNA) from waste samples. The organic ligand 2-naphthol was successfully conjugated onto the mesoporous nanospheres, which then captured SNA under suitable conditions. A naked-eye color change was observed even when a trace amount of SNA interacted with the material, which is the most promising advantage of the fabricated material. A low limit of detection and quantification limit were also determined, and the new nanosphere material revealed the ultra-trace detection performance of 0.27 µg L-1 of SNA in aqueous media. The effect of solution pH, competing ions, color optimization and initial concentration of SNA on the nanosphere material was investigated under the optimum conditions. The nanosphere material exhibited rapid adsorption properties, and its maximum adsorption capability approached 79.20 mg g-1. Several compounds were examined as common interfering substances including vanillin, glucose, lactose, starch and sucrose, which did not adversely interfere in both the detection and adsorption systems using the proposed nanosphere material. The data emphasized that the proposed material is highly suitable for the capture of SNA from contaminated water based on its selectivity, sensitivity, cost-effectiveness and eco-friendly approach. The results also indicate that this nanosphere material will attract attention from researchers for the efficient and selective capture of the toxic SNA.

Facile synthesis of magnetic disinfectant immobilized with silver ions for water pathogenic microorganism's deactivation.

One-pot synthesis of a new magnetic disinfectant was achieved through the polymerization of thiourea and formaldehyde in the presence of magnetite nanoparticles (MTUF). The obtained magnetic chelating resin was loaded with Ag(I) ions. This material was tested as a disinfectant for water pathogenic microorganism's deactivation. The toxicity of MTUF before and after Ag(I) loading was estimated. The antimicrobial activity tests of MTUF-Ag were carried out against Escherichia coli, Salmonella Typhimurium, and Pseudomonas aeruginosa as examples of Gram-negative bacteria; Listeria monocytogenes, Staphylococcus aureus, Enterococcus faecalis, and Bacillus subtilis as examples of Gram-positive bacteria; and Candida albicans as representative for fungi. The results showed that the minimum inhibitory dosage (MID) of MTF-Ag against Escherichia coli, Salmonella Typhimurium, Listeria monocytogenes, Staphylococcus aureus, and mixed culture were 1.5, 2.0, 1.0, 1.5, and 1.5 mg/mL, respectively, after 40 min of contact time. While C. albicans was more resistant to the magnetic disinfectant, only three log reductions were done at 2.5 mg/mL. The studied MTUF-Ag was successfully tested for water and wastewater pathogenic microorganism's deactivation. It can be concluded that MTUF-Ag could be a good candidate for water disinfection.

Influence of Mo(VI) immobilization and temperature on As(V) sorption onto magnetic separable poly p-phenylenediamine-thiourea-formaldehyde polymer.

The immobilization of Mo(VI) on magnetic poly p-phenylenediamine-thiourea-formaldehyde composite polymer (MpPDTF) (through an intermediary adsorption step) increased sorption of As(V) ions: retention capacity increased from 35.15mg As g-1 for MpPDTF to 99.04mg As g-1 for MpPDTF immobilized Mo(VI) at 298±1K. The impact of temperature and Mo(VI) immobilization on the kinetic and equilibrium constants of As(V) sorption on MpPDTF was evaluated. The thermodynamic study shows that Mo(VI) immobilization on MpPDTF changes the sorption process of As(V) on MpPDTF from exothermic associated with entropy decrease to endothermic associated with entropy increase. Also the impact of phosphate competition was studied. MpPDTF immobilized Mo(VI) was successfully tested for As(V) removal from the industrial effluents of insecticides manufacturing industry. NaHCO3 solution (0.5M) can be efficiently used for sorbent regeneration for at least 3 cycles with limited decrease in sorption performance.

Magnetic Schiff's base sorbent based on shrimp peels wastes for consummate sorption of chromate.

Magnetic Schiff's base chitosan composite has been prepared starting from shrimp peels as a raw material. Chitosan extraction involved three main stages as preconditioning, demineralization deproteinization and deacetylation. Chitosan modification process took place through the reaction between chitosan and polymeric Schiff's base of thiourea/glutaraldehyde in the presence of magnetite. The synthetic hybrid composite was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy-energy dispersive X-ray analyses and tested as sorbent for Cr(VI) recovery from aqueous solution. The performance of the sorbent was systematically evaluated by batch sorption experiments, followed by equilibrium and kinetic studies with different mathematical models. The isotherm study demonstrate that the sorbent achieved 99.1% (sorption capacity; 252.45 mg g-1) removal efficiency in Cr(VI) solution with concentrations up to 400 mg/L. Experimental data gave better mathematical fitting towards pseudo-second-order kinetic model and Langmuir isotherm model. The distribution coefficient was obtained at different temperatures and the thermodynamic parameters have been calculated: the sorption is endothermic, spontaneous and contributes to increase the randomness of the system. The sorbent could be recycled for three cycles of sorption/desorption.

Arsenic(V) sorption using chitosan/Cu(OH)2 and chitosan/CuO composite sorbents.

The removal of As(V) ions from aqueous solution was carried out using composite sorbents based on chitosan (as the encapsulating material) and Cu(OH)2 or CuO. The sorbents were characterized using SEM, EDX and Zeta potential analysis. Sorption uptake was highly dependent on pH, temperature, initial As(V) concentration and sorbent dosage (SD): the optimum initial pH for arsenic removal was found close to 4. The sorption isotherm was described by the Langmuir equation. The metal ion can be bound through two different sorption sites: one having a strong affinity for As(V) (probably Cu(OH)2 or CuO) and the other having a lower affinity (probably the encapsulating material). The uptake kinetics was well fitted by the pseudo-second order rate equation. The effect of temperature was also evaluated, verifying the endothermic nature of the sorption process. Arsenic elution was performed using a saline solution (30 g L(-1) NaCl) at pH 12. The recycling of the sorbent was tested, maintaining a removal efficiency and a metal recovery over 95% for five successive sorption/desorption cycles.