Azo dye removal by Moringa oleifera seed extract coagulation

In this paper, the ability of Moringa oleifera seed extract–among other natural coagulants–to remove several different types of dyes has been researched. Moringa oleifera has been demonstrated to have a high removal ability for anionic dyes. This study is particularly focused on testing the removal of an azo dye such as Chicago Sky Blue 6B (CSB). It has taken out the fast kinetic of coagulant action and the high potential of this coagulant agent to treat wastewater from dyestuff. Up to 99% of CSB removal has been achieved with M. oleifera extract dosage of 150, 200 and 250 mg l^?1 for 100, 160 and 200 mg l^?1 of initial CSB concentration, respectively. Temperature does not affect the coagulant process and a pH level greater than 8 has a negative influence. Lower CSB percentage removal is achieved by increasing the initial dye concentration, but an optimum relationship between dye amount removed and M. oleifera extract amount has been established and it appears to be between 0.7 and 0.9, depending on the initial dye concentration and the bulk of the remaining dye concentration.     

Palm oil mill effluent pretreatment using Moringa oleifera seeds as an environmentally friendly coagulant: laboratory and pilot plant studies

This research paper covers the suitability of the coagulation–flocculation process using Moringa oleifera seeds after oil extraction as a natural and environmentally friendly coagulant for palm oil mill effluent treatment. The performance of M. oleifera coagulant was studied along with the flocculant KP 9650 in removal of suspended solids, organic components and in increasing the floc size. The optimum values of the operating parameters obtained from the laboratory jar test were applied in a pilot‐scale treatment plant comprised of coagulation–flocculation and filtration processes. Pilot‐scale pretreatment resulted in 99.7% suspended solids removal, 71.5% COD reduction, 68.2% BOD reduction, 100% oil and grease removal and 91% TKN removal. In pilot plant pretreatment, the percentage recovery of water was 83.3%, and 99.7% sludge was recovered after dewatering in a filter press. Copyright © 2006 Society of Chemical Industry     

Identification of Moringa oleifera protein responsible for the decolorization and pesticide removal from drinking water and industrial effluent – an in silico and in situ evaluation

Natural products are always in demand, especially in the food and water treatment industry, to reduce health hazards caused by the prolonged use of chemicals. Though crude seed extract of Moringa oleifera (MOCE) is used for decolouration, the protein responsible for such activity is not fully known. In this study, in silico analysis of Moringa oleifera coagulant protein (MOCP; a predominant oligomeric protein in MOCE) was undertaken to check its molecular interactions with water and soil pollutants, in order to identify the protein accountable for such activities. The molecular docking studies of MOCP with azo dyes like congo red, tartrazine) and a pesticide (dichlorodiphenyltrichloroethane) revealed a strong binding affinity (?5.66, ?5.33 and ?5.04, respectively, kJ mol^?1) between the protein and the pollutants through hydrogen bonding and electrostatic interactions. Further, these results were verified in situ with MOCP, a recombinant form of MOCP (MOCRP) and MOCE against congo red (100 mg L^?1) and revealed the dye removal efficiency of 63.8%, 65.7%, and 72.3%, respectively. While the jar test results of synthetic coloured water and industrial textile effluent containing congo red showed 51.6% and 58.3%. Hence, we believe that the MOCP is responsible for multiple activities of MOCE and suggest its prospective use for large‐scale treatment of drinking water and industrial effluents. © 2014 Society of Chemical Industry     

Coagulation process for tannery industry effluent treatment using Moringa oleifera seeds protein: Kinetic study,pH effect on floc characteristics and design of a thickener unit

The kinetics of coagulation process for turbidity removal from tannery industry effluent using NaCl solution extracted Moringa oleifera protein is reported here. The effect of initial pH of effluent on floc size and strength was analysed. Floc size decrease with increase in velocity gradient and hierarchy of floc size exponent at different pH was: acidic > neutral > basic. It was observed based on the half-life period data that the process follows a second-order kinetic model with 0.000862 (L/mg min) as the rate constant. The Talmadge–Fitch method is used to analyse batch sedimentation data for the calculation of area for the clarifier-thickener unit to treat 5 m³/h of tannery wastewater.     

Decolourization of textile dyes by the white‐rot fungi Phanerochaete chrysosporium and Pleurotus ostreatus

BACKGROUND: The ability of the fungi Pleurotus ostreatus and Phanerochaete chrysosporium to decolourize and detoxify 11 (mono‐, dis‐, poly‐ azo, and anthraquinonic type) dyes, widely used across the textile and leather industries, was tested. RESULTS: Different substrate specificities were revealed between P. ostreatus and P. chrysosporium in decolourization experiments. The latter fungus provided almost complete decolourization of the tested azo dyes up to 600 ppm and dis‐azo dyes up to 1000 ppm, and 80% decolourization of the tris‐azo dye DBU1L38 at 1000 ppm, after 6 days. P. ostreatus provided almost total decolourization of the anthraquinone type dye ABU62 (1000 ppm) after just 1 day. P. ostreatus also showed the ability to decolourize the tested dis‐azo and tris‐azo dyes, giving the best performances against the dis‐azo DBU1U1 (600 ppm) dye, which was 100% decolourized after 6 days. Laccases proved to be the main enzymatic activities acting in P. ostreatus decolourization. CONCLUSION: The potential of the fungi P. ostreatus and P. chrysosporium as efficient bio‐systems for decolourization and detoxification of several toxic industrial dyes was demonstrated. The role of laccases in the decolourization of dis‐azo dyes by P. ostreatus was demonstrated for the first time. Copyright © 2008 Society of Chemical Industry     

Biosorption of Cu(II) onto agricultural materials from tropical regions

BACKGROUND: In Ghana, the discharge of untreated gold mine wastewater contaminates the aquatic systems with heavy metals such as copper (Cu), threatening ecosystem and human health. The undesirable effects of these pollutants can be avoided by treatment of the mining wastewater prior to discharge. In this work, the sorption properties of agricultural materials, namely coconut shell, coconut husk, sawdust and Moringa oleifera seeds for Cu(II) were investigated. RESULTS: The Freundlich isotherm model described the Cu(II) removal by coconut husk (R² = 0.999) and sawdust (R² = 0.993) very well and the Cu(II) removal by Moringa oleifera seeds (R² = 0.960) well. The model only reasonably described the Cu(II) removal by coconut shell (R² = 0.932). A maximum Cu(II) uptake of 53.9 mg g^?1 was achieved using the coconut shell. The sorption of Cu(II) onto coconut shell followed pseudo‐second‐order kinetics (R² = 0.997). FTIR spectroscopy indicated the presence of functional groups in the biosorbents, some of which were involved in the sorption process. SEM‐EDX analysis confirmed an exchange of Mg(II) and K(I) for Cu(II) on Moringa oleifera seeds and K(I) for Cu(II) on coconut shell. CONCLUSION: This study shows that coconut shell can be an important low‐cost biosorbent for Cu(II) removal. The results indicate that ion exchange, precipitation and electrostatic forces were involved in the Cu(II) removal by the biosorbents investigated. Copyright © 2011 Society of Chemical Industry     

Immobilization horseradish peroxidase on amine-functionalized glycidyl methacrylate-<Emphasis Type="Italic">g</Emphasis>-poly(ethylene terephthalate) fibers for use in azo dye decolorization

Activated fibers were used as a new support material for the immobilization of horseradish peroxidase (HRP). Poly(ethylene terephthalate) (PET) fibers were grafted with glycidyl methacrylate (GMA) using benzoyl peroxide (Bz₂O₂) as initiator. 1,6-diaminohexane (HMDA) was then covalently attached to this GMA grafted PET fibers. HMDA-GMA-g-PET fibers were activated with glutaraldehyde and HRP was successfully immobilized. Both on the free HRP and the immobilized HRP activities, pH, temperature, thermal stability, and reusability were investigated. Both free enzyme and immobilized enzyme were used in a batch process for the degradation of azo dye. About 98% of azo dye removal was observed with immobilized HRP, while 79% of azo dye removal was found with the free HRP. 45 min of the contact time is sufficient for the maximum azo dye removal. The HRP immobilized on modified PET fibers were very effective for removal of azo dye from aqueous solutions.     

Application of magnetic iron oxide nanoparticles prepared from microemulsions for protein purification

BACKGROUND: Magnetic nanoparticles are of immense interest for their applications in biotechnology. This paper reports the synthesis of magnetic iron oxide nanoparticles from two different water‐in‐oil microemulsion systems (ME‐MIONs), their characterization and also their use in purification of coagulant protein. RESULTS: ME‐MIONs have demonstrated to be an efficient binder in the purification of Moringa oleifera protein when compared with the superparamagnetic iron oxide nanoparticles prepared from coprecipitation in aqueous media. The size and morphology of the ME‐MIONs were studied by transmission electron microscopy (TEM) while the structural characteristics were studied by X‐ray diffraction (XRD). The microemulsion magnetic iron oxide nanoparticles (ME 1‐MION and ME 2‐MION) obtained have a size range 7–10 nm. The protein and ME‐MIONs interaction was investigated by Fourier transform infrared spectroscopy (FT‐IR); the presence of three peaks at 2970, 2910 and 2870 cm^?1 respectively, confirms the binding of the protein. The purification and molecular weight of the coagulant protein was 6.5 kDa as analyzed by SDS‐PAGE. CONCLUSION: The ME‐MIONs have the advantage of being easily tailored in size, are highly efficient as well as magnetic, cost effective and versatile; they are, thus, very suitable for use in a novel purification technique for protein or biomolecules that possess similar characteristics to the Moringa oleifera coagulant protein. Copyright © 2011 Society of Chemical Industry     

Fe(III)/H2O2-Like System for Removal of Azo Dye from Aqueous Solution

Fe(III)/H₂O₂ system is an effective method for separating the organic compounds from aqueous solution, whereas it is often investigated under lower pH conditions. In order to improve performance of the system, a Fe(III)/H₂O₂-like system that was composed of iron-based coagulant and H₂O₂ was developed, which has the combined effect of flocculation and oxidation. The system when used for decolorization of an organic azo dye solution, Procion Red MX-5B, under wider pH range, indicated higher decolorization efficiency. Parameters affecting the decolorization such as coagulant dosage, H₂O₂ concentration, initial solution pH, temperature, and initial dye concentration were examined in this study. The results indicated that with appropriate coagulant dosage, H₂O₂ concentration, and pH, it was more effective for the decolorization, especially in a weak alkaline environment (pH = 7-8); the pseudo-first-order kinetics could express the azo dye concentration as a function of the reaction time. This study further illustrated that the azo dye solution was degraded to a degree with 53.22% TOC removal at an initial total TOC concentration of 14.92 mg/L. Overall, the established system in this study was favorable to the decolorization of soluble azo dye.     

Removal of turbidity from drinking water using natural coagulants

The ability of three plant materials, seeds such as Moringa oleifera, Strychnos potatorum and Phaseolus vulgaris, to act as natural coagulants was tested using synthetic turbid water formulated to resemble the drinking water. An improved and alternative method for the extraction of the active coagulant agent M. oleifera, S. potatorum, P. vulgaris seeds was developed and compared with the conventional water extraction method. In the new method the seeds were extracted using different solvents of NaCl and NaOH to extract the active coagulant agent from natural coagulants. In addition, ultrasound was investigated as a potential method to assist the extraction process. Batch coagulation experiments were conducted to evaluate the performance of the extracted coagulant achieved through various schemes. The optimum turbidity removal at different values of initial synthetic wastewater turbidity from 100 to 500 NTU was investigated. Sodium chloride at 0.5 M was found to provide a high turbidity removal of >99% compared to NaOH and distilled water extract. Among these three coagulant M. oleifera seed extracts is the highest performance in turbidity removal. The optimum coagulant dosage showed the coagulation with blended coagulant M. oleifera, S. potatorum and P. vulgaris. The study was carried out for initial turbidity of the sample such as 100 NTU (low), 250 NTU (medium) and 500 NTU (high). For the natural coagulant dosage was found to be 250–1000 mg/L respectively. It was found that the percentage of removal is highest in M. oleifera.     

THE EFFECT OF ENVIRONMENTALLY BENIGN FRUIT EXTRACT OF SHAHJAN (MORINGA OLEIFERA) ON THE CORROSION OF MILD STEEL IN HYDROCHLORIC ACID SOLUTION

The inhibition of the corrosion of mild steel in hydrochloric acid solution by the fruit extract of shahjan (Moringa oleifera) was studied using weight loss, electrochemical impedance spectroscopy (EIS), linear polarization, and potentiodynamic polarization techniques (Tafel). Inhibition was found to increase with increasing concentration of the extract. The effect of temperature, immersion time, and acid concentration on the corrosion behavior of mild steel in hydrochloric acid solutions with addition of extract was also studied. The inhibition occurred via adsorption of the inhibitor molecules on the mild steel surface obeying the Langmuir adsorption isotherm. Thermodynamic activation parameters such as activation energy, enthalpy (ΔH*), and entropy (ΔS*) of activation for corrosion process were calculated and discussed. The results obtained show that both chemical and physical adsorption of inhibitor molecules occur simultaneously and the fruit extract of shahjan (Moringa oleifera) could serve as an effective inhibitor of the corrosion of mild steel in hydrochloric acid media.     

Optimum Coagulant from Acacia mearnsii de Wild for Wastewater Treatment

A novel coagulant agent from Acacia mearnsii de Wild tannin extract was characterized for removal of the anthraquinonic colorant Alizarin Violet 3R and the anionic surfactant sodium dodecylbenzene sulfonate. This coagulant is the result of a previous optimization study. The influence of operative variables such as temperature, coagulant dosage, initial pollutant content, and pH was investigated. The new coagulant demonstrates a high affinity for dye and surfactant and is efficient within a wide range of working conditions. While the temperature does not affect the coagulant ability, an acidic pH seems to increase the contaminant removal from aqueous solutions. Implementation in a pilot plant confirms the feasibility of this coagulant not only at lab scale, but also at higher level.     

Biocorrosion inhibition of mild steel in crude oil-water environment using extracts of Musa paradisiaca peels,Moringa oleifera leaves,and Carica papaya peels as biocidal-green inhibitors: kinetics and adsorption studies

Biocorrosion inhibition of mild steel in the crude oil-water environment was investigated in the absence and presence of Carica papaya peel extract, Musa paradisiaca peel extract, and Moringa oleifera leaf extract as potential biocidal-green inhibitors using gravimetric, polarization, and surface analysis (Inverted metallurgical microscope and Fourier transform infra-red spectroscopy) methods. Kinetics and adsorption behaviors of the extracts were determined and evaluated. Results revealed that each of the extracts functioned as biocidal-green inhibitors in the crude oil-water environment and that biocorrosion inhibition efficiency (IE%) of each extract increased with increase in extract concentration and exposure time. Maximum IE% of 97.7, 96.5, and 99.2% was achieved with Musa paradisiaca peel extract, Moringa oleifera leaf extract, and Carica papaya peel extract, respectively, at 4000?mg/l extract concentration and 35 d exposure time. Polarization studies indicated that each of the extracts acts as a mixed-type inhibitor. Mild steel susceptibility to biocorrosion was significantly reduced by each of the extracts through biofilm development suppression and extract adsorption onto the mild steel surface which obeyed Langmuir, Freundlich, Temkin, and Flory-Huggins isotherm models. Kinetics of mild steel biocorrosion inhibition followed a Monod form of kinetics (Type A). Gibbs free energy of adsorption values for Musa paradisiaca peel extract (?9.65?kJ/mol), Moringa oleifera leaf extract (?9.57?kJ/mol), and Carica papaya peel extract (?9.71?kJ/mol) showed that each extract adsorption was spontaneous and of physical adsorption.     

Heterogeneous catalyzed biodiesel production from Moringa oleifera oil

In this study, biodiesel was produced from Moringa oleifera oil using sulfated tin oxide enhanced with SiO₂ (SO₄²⁻/SnO₂-SiO₂) as super acid solid catalyst. The experimental design was done using design of experiment (DoE), specifically, response surface methodology based on three-variable central composite design (CCD) with alpha (α) = 2. The reaction parameters studied were reaction temperature (60 °C to 180 °C), reaction period (1 h to 3 h) and methanol to oil ratio (1:6 to 1:24). It was observed that the yield up to 84 wt.% of Moringa oleifera methyl esters can be obtained with reaction conditions of 150 °C temperature, 150 min reaction time and 1:19.5 methanol to oil ratio, while catalyst concentration and agitation speed are kept at 3 wt.% and 350-360 rpm respectively. Therefore this study presents the possibility of converting a relatively new oil feedstock, Moringa oleifera oil to biodiesel and thus reducing the world's dependency on existing edible oil as biodiesel feedstock.     

Electrochemical degradation of the Acid Blue 62 dye on a β-PbO<Subscript>2</Subscript> anode assessed by the response surface methodology

The electrochemical degradation of the anthraquinonic dye Acid Blue 62 in a filter-press reactor on a Ti/Pt/β-PbO₂ anode was investigated using the response surface methodology with the variables: current density, pH, [NaCl], and temperature. The system’s modeling was carried out with the charge required for 90% decolorization (Q ⁹⁰) and the chemical oxygen demand removal percentage after a 30 min electrolysis (COD ³⁰), with good correlations between predicted and observed values. Best conditions for decolorization were attained in acidic solutions (pH = 4) with medium to high [NaCl] (1.0–2.0 g L⁻¹) and lower temperature due to the prevalent oxidant species HOCl and Cl₂. Optimal conditions for COD ³⁰ removal were attained at high current densities in pH > 5 solutions with high [NaCl], when the prevalent oxidant species are HOCl and OCl⁻. The lowest charge per unit volume of the electrolyzed solution necessary for total mineralization was attained at pH 11.     

结构态亚铁羟基化合物还原预处理印染废水的效果和机制

印染废水的脱色是重要的处理难题。以6种偶氮染料模拟废水和实际印染废水为目标污染物,研究了亚铁羟基化合物(ferrous hydroxy complex ,FHC)还原预处理印染废水的效果和机理。通过亚铁结构形态、初始pH、FHC投加量、Fe/OH^-摩尔比等因素对FHC还原转化染料的影响研究,综合评价了FHC对多种偶氮染料的反应性能。实验结果表明FHC具有较高的还原活性,投加89.6 mg·L^-1的FHC,可以去除90%以上的偶氮染料。亚铁结构形态对还原脱色有很大影响,溶解态亚铁基本不能还原偶氮染料,结构态亚铁FHC相似文献   

Azoic dyes hosted on hydrotalcite-like compounds: Non-toxic hybrid pigments

Layered double hydroxides with the hydrotalcite type structure and a Mg:Al ratio of three have been prepared with an azoic dye (methyl orange) stabilized on the external surface. Methyl orange was incorporated by reconstruction from a mildly calcined LDH-CO₃ precursor. The solids have been characterized by powder X-ray diffraction and FTIR, UV–vis and ²⁷Al, ¹³C CP/MAS NMR spectroscopies. Hartree–Fock calculations were performed in order to investigate the guest-host arrangement. Results show that the methyl orange molecule is in configuration trans and that the carbons in α- and β-positions, relative to the azo group, are interacting directly with brucite-like layers. Hydrotalcite shows a very high affinity for retention of azoic dyes. Another advantage offered by the stabilization of methyl orange anions in hydrotalcites compounds is that they are shielded from acid attacks.     

Coagulation and flocculation of dye-containing solutions using a biopolymer (Chitosan)

Chitosan, dissolved in acetic acid, was used for the coagulation–flocculation of an anionic dye (Reactive Black 5). In acidic solutions protonated amine groups of chitosan attract dye sulfonic groups. Increasing chitosan dosage increases dye removal up to a concentration resulting in complete neutralization of anionic charges; above, the excess of cationic charges leads to suspension re-stabilization. Process efficiency increases with decreasing the initial pH of dye solution: the molar ratio between dye molecules and amine groups ([n]) respects the stoichiometry between sulfonic functions and protonated amine groups at initial pH 5; at initial pH 3 a possible dye aggregation phenomenon results in higher molar ratio [n]. The coefficient [n] depends on both the pH and the molecular weight of chitosan. The main mechanism for dye coagulation with chitosan sounds to be charge neutralization at acidic pH.     

Degradation of an Azo Dye (Ponceau 4R) and Treatment of Wastewater from a Food Industry by Ozonation

Experiments for degradation of the extensively marketed Ponceau 4R dye in aqueous solution and for oxidation of raw wastewater from a confectionary industry have been carried out by using ozone. All the experiments were performed in a cylindrical semi-batch reactor at approximately 20 ^oC for 7200 s. A mass flow rate of 1.158?×?10^?6 kg s^?1 of ozone was continuously fed in the reactor. The pH of the azo dye aqueous solution (distilled water + Ponceau 4R) was always kept at approximately 5.8, while in the case of the raw wastewater the same factor was changed from 4.7 to 9.4 in two different experimental runs. Absorbance measurements at 508 nm show that the investigated azo dye found in the azo dye aqueous solution was completely degraded after only 600 s. At this initial period a substantial fall of TOC (Total Organic Carbon) (up to 45%) was noticed, but the rate was exponentially decreased at longer reaction times up to a TOC removal no higher than 60%. The ozonation was also responsible for reducing the apparent color of the raw wastewater to almost 10% of its initial value at the optimum pH (9.4 ± 1.5). The effect of pH was important on apparent color, but it had absolutely no influence on the kinetics results of COD (Chemical Oxygen Demand), which were kept constant over the entire period of reaction.     

Biotechnological Potential of Soil Isolate,Flavobacterium mizutaii for Removal of Azo Dyes: Kinetics,Isotherm, and Microscopic Study

Flavobacterium mizutaii has been isolated from soil samples for efficient removal of two azo dyes that is, napthol blue black (Color Index 20470) and direct red 80 (Color Index 35780). The adsorption behaviors of these azo dyes have been investigated in detail to explore the potentiality of F. mizutaii in pollution control management. Effects of various conditions such as pH, temperature, dye concentrations, and incubation time have been studied to optimize the adsorption process. The process is found to be a function of pH of the solution, with the optimum range being pH 1.0–2.0. The results also establish that 405.82 ± 51.4 µmol of napthol blue black and 253.15 ± 31.8 µmol of direct red 80 are adsorbed per gram of F. mizutaii at optimum conditions. FTIR spectroscopic study and functional groups modifications demonstrates different functional groups viz. carboxyl, amine, and phosphate groups of the cell wall components responsible for adsorption of the dyes. AFM along with TEM analysis demonstrates a conspicuous surface morphology change of the dye-adsorbed biomass.

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