Kinetics of sorptive removal of chromium(VI) from aqueous solutions by calcined Mg-Al-CO(3) hydrotalcite

The sorptive removal of hexavalent chromium from aqueous solutions by calcined Mg-Al-CO(3) hydrotalcite was investigated in a batch mode. The influence of agitation speed, solution pH, initial chromium concentration, sorbent concentration and temperature has been tested in kinetic runs. Three kinetic models have been evaluated to fit the experimental data: the pseudo-first order, the modified-second order and the Elovich equation. It was shown that the first-order model could best describe the sorption kinetics. A Freundlich isotherm was used to fit equilibrium experiments. Hydrotalcite presents a sorption capacity of approximately 120 mg Cr/g, under the investigated experimental conditions. The calculated activation energy for process studied was around 40 kJ/mol.     

Experimental study and modelling of Cr (VI) removal from wastewater using Lemna minor

The removal of Cr(VI) from wastewater by Lemna minor was studied both at laboratory and pilot scale. Laboratory tests were conducted under different conditions of initial Cr(VI) concentration (0.5 and 2.0 mg/l) and temperature (285 and 291 K). Batch experiments were carried out during 16 days in which the chromium concentrations, both in the biomass and in wastewater were measured. Data were used to characterize the biouptake capacity of the biomass; results showed that it increases with the temperature and when the initial Cr concentration decreases. The biouptake process could be fitted by an equation, with a correlation coefficient of 0.98. The removal process was assessed using the data of the variation of chromium concentration in the wastewater with respect to time; this allowed obtaining constant parameters which were applied in a mathematical model for the assessment of duckweed systems in a pilot scale plant.     

Removal of chromium (VI) from wastewater using bentonite-supported nanoscale zero-valent iron

Bentonite-supported nanoscale zero-valent iron (B-nZVI) was synthesized using liquid-phase reduction. The orthogonal method was used to evaluate the factors impacting Cr(VI) removal and this showed that the initial concentration of Cr(VI), pH, temperature, and B-nZVI loading were all importance factors. Characterization with scanning electron microscopy (SEM) validated the hypothesis that the presence of bentonite led to a decrease in aggregation of iron nanoparticles and a corresponding increase in the specific surface area (SSA) of the iron particles. B-nZVI with a 50% bentonite mass fraction had a SSA of 39.94 m²/g, while the SSA of nZVI and bentonite was 54.04 and 6.03 m²/g, respectively. X-ray diffraction (XRD) confirmed the existence of Fe⁰ before the reaction and the presence of Fe(II), Fe(III) and Cr(III) after the reaction. Batch experiments revealed that the removal of Cr (VI) using B-nZVI was consistent with pseudo first-order reaction kinetics. Finally, B-nZVI was used to remediate electroplating wastewater with removal efficiencies for Cr, Pb and Cu > 90%. Reuse of B-nZVI after washing with ethylenediaminetetraacetic acid (EDTA) solution was possible but the capacity of B-nZVI for Cr(VI) removal decreased by approximately 70%.     

Removal and recovery of Cr(VI) from polluted ground waters: a comparative study of ion-exchange technologies

The focus of this work has been the study of Cr(VI) removal from ground waters and the simultaneous concentration for its reuse using three different technological alternatives: anion-exchange resins, liquid-liquid extraction assisted by hollow fibre membranes and emulsion pertraction. The viability of the considered objectives, i.e., Cr(VI) separation (<0.5 g/m3) and concentration for reuse (>20,000 g/m3) has been checked and a comparative analysis of the three technologies has been performed. Although the flexibility and ease of operation of non-dispersive solvent extraction, anion-exchange resins and emulsion pertraction lead to higher velocities of chromium removal, yet still maintaining similar concentration efficiencies.     

Visible light induced photocatalytic reduction of Cr(VI) over polymer-sensitized TiO2 and its synergism with phenol oxidation

In this study, both Cr(VI) reduction and phenol oxidation induced by polymer-sensitized TiO₂ were investigated under visible light. Study of the reaction mechanism indicated that poly(fluorene-co-thiophene) (PFT) acted as a semiconductor and was by itself able to reduce Cr(VI) under visible light irradiation. When coupled with TiO₂, PFT served not only as the electron donor for Cr(VI) reduction, but also as a sensitizer. Upon irradiation by visible light, electrons in the sensitizing PFT polymer are excited and are transferred to the conduction band of TiO₂. PFT-catalyzed reduction of Cr(VI) was significantly promoted by the presence of phenol, and synergism between Cr(VI) reduction and phenol degradation was demonstrated both by analysis of the FT-IR spectrum of PFT/TiO₂ and by measuring the effect of repeated use of PFT/TiO₂ on its photocatalytic efficiency. The results provide a cost-effective method to remove organic and inorganic pollutants simultaneously in the complex wastewater.     

Comparative and competitive adsorption of Cu(II), Cd(II) and Pb(II) onto Sepia pharaonis endoskeleton biomass from aqueous solutions

In this research, the possibility of simultaneous removal of lead, cadmium and copper divalent ions from water samples through the use of Sepia pharaonis endoskeleton powder (SPEB) as bio‐material, was investigated. The bio‐sorbent was characterised by Fourier transform infrared spectrum (FT‐IR), atomic force microscopy (AFM) and X‐ray fluorescence (XRF). The different factors affecting the bio‐sorption process were studied. Langmuir and Freundlich isotherm models were applied to analyse the experimental data. The kinetic studies showed that the pseudo‐second order model kinetics were compatible with the investigated systems. It was found that under optimal conditions, this bio‐sorbent was efficient in the uptake of these heavy metal ions from both mono and multi‐metal solutions, and high removal percentages were achieved. This study verified the potential ability of SPEB as an efficient natural adsorbent for removal of Pb(II), Cd(II) and Cu(II) ions from river, tap and mineral water samples.     

Removal of quinol from aqueous solution by adsorption onto Fe(III)/Cr(III) hydroxide and application to real effluent treatment

The adsorption capacity of ‘waste’ Fe(III)/Cr(III) hydroxide for removal of quinol at varying agitation time, quinol concentration, adsorbent dose, pH and temperature was investigated by batch method. The Langmuir isotherm was found to represent the equilibrium sorption data well and the adsorption capacity was found to be 24.4 mg g^?1 and 28.2 mg g^?1 for untreated and pre‐treated adsorbent, respectively. Adsorption followed second‐order kinetics. Adsorption was maximum and uniform in the pH range 4.0–10.0 and 6.0–10.0 for untreated and pre‐treated adsorbent, respectively. The adsorption was endothermic in nature. Application of the adsorbent to the treatment of real effluent was demonstrated.     

Production, composition and Pb2+ adsorption characteristics of capsular polysaccharides extracted from a cyanobacterium Gloeocapsa gelatinosa

Pb²⁺ adsorption by the living cells of the cyanobacterium Gloeocapsa gelatinosa was studied. Cyanobacterial cells with intact capsular polysaccharide (CPS) showed 5.7 times higher Pb adsorption capacity than that of cells without CPS. The adsorbed Pb was desorbed by EDTA, indicating that Pb²⁺ adsorption occurred mainly on cell surface. Production, sugar content and ability of CPS to remove Pb²⁺ were then studied in details. CPS production by G. gelatinosa increased when culture time was prolonged. The maximum CPS production was 35.43 mg g⁻¹ dry weight after 30-day cultivation. Xylose, arabinose, ribose, rhamnose, galactose, glucose, mannose and fructose were the neutral sugars presented in CPS of G. gelatinosa. Acidic sugars including galacturonic and glucuronic acids were also found in CPS. The amount and composition of G. gelatinosa's CPS varied according to its growth phase and culture conditions. The highest amount of acidic sugars was produced when cultured under low light intensity. The extracted CPS rapidly removed Pb²⁺ from the solution (82.22±4.82 mg Pb²⁺ per g CPS), directly demonstrating its roles in binding Pb²⁺ ions. Its ability to remove Pb²⁺ rapidly and efficiently, to grow under sub-optimal conditions (such as low pH and low light intensity), and to produce high amount of CPS with acidic sugars, leads us to conclude that G. gelatinosa is a potential viable bioadsorber for mildly acidic water contaminated with Pb²⁺.     

Comparative study of the uses of poly(4-vinylpyridine) and poly(diallyldimethylammonium) chloride for the removal of perchlorate from aqueous solution by polyelectrolyte-enhanced ultrafiltration

An application of polyelectrolyte-enhanced ultrafiltration utilizes cationic polyelectrolytes to electrostatically bind anionic species. The colloid and target anion are then concentrated using an ultrafilter, producing a filtrate with a lower concentration of the target. This study compared the performances of poly(4-vinylpyridine) (P4VP) and poly(diallyldimethylammonium) chloride (PDADMAC) for the removal of perchlorate. Potentiometric titration data revealed that the ionization properties of P4VP in aqueous solution vary as functions of titrant utilized, degree of protonation, and counterion concentration. The greater affinity of perchlorate over chloride for the protonated pyridine residues of P4VP provided up to 95.8% retention of perchlorate under the solution conditions investigated. Through ultrafiltration experiments, the effects solution pH, counterion concentration, and polymer concentration were examined for both P4VP and PDADMAC. In addition, the effectiveness of P4VP recovery and reuse was also assessed.     

Sorption of Pb2+ from aqueous solution using polyethylene and polyvinylchloride wastes as adsorbents: a comparative study

This study gives insight into the sorption potential of Pb²⁺ from aqueous solution using polyethylene and polyvinylchloride wastes as adsorbent. The polymer samples were characterised by X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), and scanning electron microscopy (SEM) for their morphological features. Kinetic, equilibrium and thermodynamic batch adsorption experiments investigated varying parameters such as: concentration, temperature and time. The SEM images of the polymers revealed irregular small size particles, indicating a high surface area and porosities facilitating sorption. The adsorption studies documented relatively rapid Pb²⁺ uptake by the polymers that are mainly diffusion controlled, with a second order kinetic process. The sorption of Pb²⁺ onto the polymer surfaces was thermodynamically favoured at relatively low temperature (low energy). Thermodynamic studies demonstrated exothermic physi-sorption mechanisms for Polyethylene (PE) and Polyvinylchloride (PVC).     

A study of external mass transfer effect on biodegradation of phenol using low‐density polyethylene immobilized Bacillus flexus GS1 IIT (BHU) in a packed bed bioreactor

The impact of external mass transport on the biodegradation rate of phenol in a packed bed bioreactor (PBBR) was studied. A potential bacterial species, Bacillus flexus GS1 IIT (BHU), was isolated from the petroleum‐contaminated soil. Low‐density polyethylene (LDPE) immobilized with the B. flexus GS1 IIT (BHU) was used as packing material in the PBBR. The PBBR was operated by varying the inlet feed flow rate from 4 to 10 mL/min, and the corresponding degradation rate coefficients were found to be in the range of 0.119–0.157 L/g h. In addition, the highest removal rate of phenol was obtained to be 1.305 mg/g h at an inlet feed rate of 10 mL/min. The external mass transfer was studied using the model . A new empirical correlation for the biodegradation of phenol in the PBBR was developed after the evaluation at various values of K and n.     

Role of cell surface components on Cu2+ adsorption by Pseudomonas putida 5-x isolated from electroplating effluent

A gram-negative bacterium Pseudomonas putida 5-x with high Cu2+ accumulating capability was isolated from electroplating effluent in Kwun Tong, Hong Kong. The pretreated cells without superficial layer-capsule, isolated cell envelopes and the separated peptidoglycan layer materials were obtained from fresh P. putida 5-x cells, their Cu2+ adsorption capacities and properties were compared with that of the fresh cells. Pretreatment by 0.1 mol L(-1) HCl enhanced Cu2+ adsorption capacity due to the degradation of cell superficial layer-capsule of P. putida 5-x cells. Isolated cell envelopes possessed five times more Cu2+ adsorption capacity than that of fresh intact cell. The Cu2+ adsorption of separated peptidoglycan layer materials indicated that the peptidoglycan layer only played 10-15% part of the Cu2+ adsorption capacity, and implied other cell surface components such as outer membrane or inner membrane might play an important role in such high Cu2+ binding of the cell envelopes. The adsorption process of fresh cells, pretreated cells and cell envelopes of P. putida 5-x could be described with Freundlich isotherm, while the adsorption of Cu2+ by separated peptidoglycan layer materials was better described with Langmuir isotherm.     

Tunnel roof deflection in blocky rock masses as a function of joint spacing and friction – A parametric study using discontinuous deformation analysis (DDA)

The stability of underground openings excavated in a blocky rock mass was studied using the discontinuous deformation analysis (DDA) method. The focus of the research was a kinematical analysis of the rock deformation as a function of joint spacing and friction. Two different opening geometries were studied: (1) span B = h_t; (2) B = 1.5h_t; where the opening height was h_t = 10 m for both configurations. Fifty individual simulations were performed for different values of joint spacing and friction angle. It was found that the extent of loosening above the excavation was predominantly controlled by the spacing of the joints, and only secondarily by the shear strength. The height of the loosening zone h_r was found to be dependent upon the ratio between joint spacing and excavation span S_j/B: (1) h_r < 0.56B for S_j/B  2/10; (2) stable arching within the rock mass for S_j/B  3/10. The results of this study provide explicit correlation between geometrical features of the rock mass, routinely collected during site investigation and excavation, and the expected extent of the loosening zone at the roof, which determines the required support.