Aluminum dispersed bamboo activated carbon production for effective removal of Ciprofloxacin hydrochloride antibiotics: Optimization and mechanism study.

The central composite rotatable design (CCD) of response surface methodology (RSM) was used to optimize aluminum dispersed bamboo activated carbon preparation. The independent variables selected for optimization are activating agent (AlCl3) concentration (mol/L), activation temperature (°C), and activation time (min.). The independent variable's response change was observed through the percentage adsorption efficiency of Ciprofloxacin hydrochloride (CIP) antibiotics. The maximum CIP adsorption efficiency was found to be 93.6 ± 0.36% (13.36 mg/g) for the adsorbent prepared at AlCl3 concentration 2.0 mol/L, activation temperature 900 °C, and activation time 120 min. The adsorption efficiency was recorded at the natural pH (7.9) of the adsorbent (3 g/L)-adsorbate (50 mL solution of 50 ppm) mixture. The Al-dispersed bamboo activated carbon was characterized for its surface morphology, surface elemental compositions, molecular crystallinity, surface area, pore morphology, and surface functional groups. The mechanism of adsorbent surface formation and CIP adsorption sites were explored. The characterization data and mechanism study will help in deciding possible future applications in other fields of study.

Groundwater fluoride removal using modified mesoporous dung carbon and the impact of hydrogen-carbonate in borehole samples.

There have been many research reports pertained to the interference of co - ions including hydrogen carbonate against the removal of fluoride from water. In this context, the present research explores the fluoride removal efficiency of ammonium carbonate modified dung derived carbon (DDC500) in the absence and presence of hydrogen carbonate using synthetically made fluoride solutions and groundwater samples. The adsorbent DDC500 was found to achieve the highest removal of 80% of fluoride at pH 6.95 than the washed carbon (DDC500W) and dung ash (DA) of 48% and 23% respectively. In DDC500, the carbon base in concert with inorganic residues actively functioned in the fluoride removal process and chosen for synthetic fluoride solutions (2-5 mg L-1) and 16 groundwater samples (2.1-3.6 mg L-1) from 10 locations of Usilampatti Taluk in Madurai District, South India. After the removal of hydrogen carbonate in groundwater, the percentage of samples was increased in accordance with the safe limits of World Health Organization (WHO) and Bureau of Indian Standard (BIS). Langmuir isotherm model (R2 = 0.9379) was in concordance with the adsorption of fluoride from groundwater free from hydrogen carbonate. The dynamics of other groundwater quality parameters at conditions and the independency between F-/HCO3- ratio and DE were illustrated by scatter plots. Characterization studies for the dried dung (CD110), derived carbons (DDC500 and DDC500W) and ashes (CD110A, DDC500A and DDC500WA) using FE-SEM, XRD, FTIR, Raman and TGA - EGA were done to understand the nature and behavior of materials.

Effect of co-existing ions during the preparation of alumina by electrolysis with aluminum soluble electrodes: structure and defluoridation activity of electro-synthesized adsorbents.

The electrochemical dissolution of aluminum was carried out to prepare hydrated aluminas which were characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), chemical titrations and defluoridation activities. Aluminas were obtained at controlled pH depending upon the counter cations of the electrolyte. A boehmite AlOOH phase was isolated mainly in ammonium solution, while aluminas synthesized in the other media contained a mixture of phases, usually both boehmite and bayerite γ-Al(OH)3. All the boehmite phases contained nano-crystallites of less than 3 nm. Batch defluoridation experiments revealed a second influence of the original electrolyte. Aluminas were very effective in defluoridation with abatement rates of 99.5%, 98.5% and 97.3% from neutral fluoride solution at 10 mgL(-1) when they were prepared in solution of (NH4)2SO4, (NH4)HCO2 and NH4Cl, respectively. The maximum fluoride capacities were 46.94; 10.25 and 12.18 mg g(-1) for aluminas prepared in solution of (NH4)2SO4; (NH4)HCO2 and NH4Cl, respectively. The amount of dissolved Al was found to be less than 0.19 mgL(-1) at neutral pH. These results show that a defluoridation with electro-synthesized aluminas would be more efficient and safe than a direct electrocoagulation.

Treatment of dairy effluents by electrocoagulation using aluminium electrodes.

This work sets out to examine the efficiency of an electrolytic treatment: electrocoagulation, applied to dairy effluents. The experiments were carried out using a soluble aluminium anode on artificial wastewater derived from solutions of milk powder. The flocks generated during this treatment were separated by filtration. The analysis of the filtrates showed that the chemical oxygen demand (COD) was reduced by up to 61% while the removal of phosphorus, nitrogen contents, and turbidity were 89, 81 and 100%, respectively. An analogous treatment applied to phosphate and lactose solutions revealed that lactose was not eliminated, a fact that could account for the rather poor lowering of the COD. Compared to the chemical coagulation treatment with aluminium sulphate, the efficiency of the electrocoagulation technique was almost identical. However the wastewaters treated by electrocoagulation differed by the fact that they exhibited a lower conductivity and a neutral pH value (by contrast to the acid nature of the solution treated by the chemical coagulation). This result (low conductivity, neutral pH) tends to show that it may be possible to recycle the treated water for some industrial uses. Moreover, the electrocoagulation process uses fewer reagents: the mass of the aluminium anode dissolved during the treatment is lower compared to the quantity of the aluminium salt used in chemical coagulation. These two observations clearly show that the electrocoagulation technique is more performing.

Mercury(II) removal from water by electrocoagulation using aluminium and iron electrodes.

In this work, electrocoagulation was used to evaluate the treatment of synthetic solutions containing mercury(II) of concentration 2 x 10(-5)M. The effects of the distance between the electrodes, current density, charge loading and initial pH on the removal efficiency were investigated, using aluminium and iron electrodes. Analysis of the filtrates resulting from the treatment was made by anodic redissolution in the differential pulse mode. The removal efficiency was above 99.9% when the distance between the electrodes was 3 cm, the current density ranging from 2.5 to 3.125 A dm(-2); for instance, 99.95% of the mercury(II) was eliminated when a charge loading of 9.33 and 15.55 F m(-3) were used for iron and aluminium respectively. In these conditions, by varying the pH of the mercury(II) solutions from 3 to 7, the removal efficiency remained higher than 99%. In addition, some experiments were carried out on a river water contaminated with mercury(II) ions, and the results obtained showed that the presence of organic matter do not influence the efficiency of the treatment. The elimination of mercury(II) ions is best performed with iron, where 15 min of electrolysis was sufficient to reach the highest removal compared to aluminium which required 25 min for the same result.

Validation of a new method using the reactivity of electrogenerated superoxide radical in the antioxidant capacity determination of flavonoids.

This article lays out a new method to measure the antioxidant capacity of some flavonoids. The methodology developed is based on the kinetics of the reaction of the antioxidant substrate with the superoxide radical (O(2)(*-)). A cyclic voltammetric technique was used to generate O(2)(*-) by reduction of molecular oxygen in aprotic media. In the same experiment the consumption of the radical was directly measured by the anodic current decay of the superoxide radical oxidation in the presence of increasing concentrations of antioxidant substrate. The method was statistically validated on flavonoid monomers and on the standard antioxidants: trolox, ascorbic acid and phloroglucinol. The linear correlations between the anodic current of O(2)(*-) and the substrate concentration allowed the determination of antioxidant index values expressed by the substrate concentration needed to consume 30% (AI(30)) and 50% (AI(50)) of O(2)(*-) in given conditions of oxygen concentration and scanning rate. The fidelity of the method was examined intraday and interlaboratories.

Electrolytic arsenic removal for recycling of washing solutions in a remediation process of CCA-treated wood.

The remediation of chromated copper arsenate or CCA-treated wood is a challenging problem in many countries. In a wet remediation, the recycling of the washing solutions is the key step for a successful process. Within this goal, owing to its solubility and its toxicity, the removal of arsenic from washing solution is the most difficult process. The efficiency of arsenic removal from As(III) solutions by electrolysis was investigated in view of the recycling of acidic washing solutions usable in the remediation of CCA-treated wood. Electrochemical reduction of As(III) is irreversible and thus difficult to perform at carbon electrodes. However the electrolytic extraction of arsenic can be performed by the concomitant reduction of the cupric cation and arsenite anion. The cathodic deposits obtained by controlled potential electrolysis were analyzed by X-ray diffraction (XRD) and energy dispersive X-ray microanalysis. XRD diffraction data indicated that these deposits were mixtures of copper and copper arsenides Cu(3)As and Cu(5)As(2). Electrolysis was carried out in an undivided cell with graphite cathode and copper anode, under a controlled nitrogen atmosphere. The evolution of arsine gas AsH(3) was not observed under these conditions.