Distribution of iron in activated carbon composites: assessment of arsenic removal behavior

2015 ◽  
Vol 15 (5) ◽  
pp. 990-998 ◽  
Author(s):  
Trishikhi Raychoudhury ◽  
Ferry Schiperski ◽  
Traugott Scheytt
Keyword(s):  
Activated Carbon ◽  
Removal Efficiency ◽  
Arsenic Removal ◽  
Iron Concentration ◽  
Granular Activated Carbon ◽  
Model Fit ◽  
Solution Ph ◽  
First Order Kinetics ◽  
Kinetics Of ◽  
Partitioning Behavior

The main objectives of this study were to evaluate the effectiveness of using iron impregnated granular activated carbon (AC) to remove arsenic from water and to assess the partitioning behavior of arsenic under a variety of conditions. Iron impregnated granular activated carbon (AC-Fe) composites were prepared with different ferric (Fe+3) concentrations, ranging from 0.09 to 3.0 M. These AC-Fe composites were able to remove 92–98% of the arsenate [As(V)] and 42–65% of the arsenite [As(III)]. The composite containing the lowest iron concentration (1.54%) was the most effective at arsenic sorption. Langmuir model fit indicated that the maximum 125 mg As(V)/gFe and 98.4 mg As(III)/gFe can be sorbed by the composite. The kinetics of arsenic sorption is well explained by pseudo first-order kinetics. The arsenate removal efficiency was found to decrease with increasing solution pH, while the As(III) removal efficiency was found to increase. The background ionic strength (IS) had no significant effect of on As(V) removal, but As(III) removal increased when the IS was greater than 50 mM NaCl. Our results indicate that a small amount of iron embedded efficiently in AC may have considerable potential in removing arsenic from water.

Kinetic of oxidation of methyl orange by vanadium(V) under conditions VO2+ and decavanadates coexist: Catalysis by Triton X-100 micellar medium

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Methyl Orange ◽  
Solution Ph ◽  
Vanadium Concentration ◽  
Limiting Behavior ◽  
First Order ◽  
First Order Kinetics ◽  
Ph Range ◽  
Kinetic Pattern ◽  
Triton X ◽  
Kinetics Of

The kinetics of oxidation of methyl orange by vanadium(V) {V(V)} has been investigated in the pH range 2.3-3.79. In this pH range V(V) exists both in the form of decavanadates and VO2+. The kinetic results are distinctly different from the results obtained for the same reaction in highly acidic solution (pH < 1) where V(V) exists only in the form of VO2+. The reaction obeys first order kinetics with respect to methyl orange but the rate has very little dependence on total vanadium concentration. The reaction is accelerated by H+ ion but the dependence of rate on [H+] is less than that corresponding to first order dependence. The equilibrium between decavanadates and VO2+ explains the different kinetic pattern observed in this pH range. The reaction is markedly accelerated by Triton X-100 micelles. The rate-[surfactant] profile shows a limiting behavior indicative of a unimolecular pathway in the micellar pseudophase.

scholarly journals Modeling of the adsorption kinetics of zinc onto granular activated carbon and natural zeolite

2006 ◽  
Vol 71 (8-9) ◽  
pp. 957-967 ◽  
Author(s):  
Ljiljana Markovska ◽  
Vera Meshko ◽  
Mirko Marinkovski
Keyword(s):  
Mass Transfer ◽  
Activated Carbon ◽  
Simulation Study ◽  
Natural Zeolite ◽  
Granular Activated Carbon ◽  
Model Parameters ◽  
Mass Transfer Resistance ◽  
External Mass Transfer ◽  
Transfer Resistance ◽  
Kinetics Of

The isotherms and kinetics of zinc adsorption from aqueous solution onto granular activated carbon (GAC) and natural zeolite were studied using an agitated batch adsorber. The maximum adsorption capacities of GAC and natural zeolite towards zinc(II) from Langmuir adsorption isotherms were determined using experimental adsorption equilibrium data. The homogeneous solid diffusion model (HSD-model) combined with external mass transfer resistance was applied to fit the experimental kinetic data. The kinetics simulation study was performed using a computer program based on the proposed mathematical model and developed using gPROMS. As the two-mass transfer resistance approach was applied, two model parameters were fitted during the simulation study. External mass transfer and solid phase diffusion coefficients were obtained to predict the kinetic curves for varying initial Zn(II) concentration at constant agitation speed and constant adsorbent mass. For any particular Zn(II) - adsorbent system, k f was constant, except for the lowest initial concentration, while D s was found to increase with increasing initial Zn(II) concentration.

scholarly journals Iron-impregnated granular activated carbon for arsenic removal: Application to practical column filters

2019 ◽  
Vol 239 ◽  
pp. 235-243 ◽  
Author(s):  
Mahatheva Kalaruban ◽  
Paripurnanda Loganathan ◽  
Tien Vinh Nguyen ◽  
Tanjina Nur ◽  
Md Abu Hasan Johir ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Arsenic Removal ◽  
Granular Activated Carbon

Application of Carbonaceous Materials to Phenol Removal from Aqueous Solution by Adsorption

2012 ◽  
Vol 164 ◽  
pp. 297-301 ◽  
Author(s):  
Wei Fang Dong ◽  
Li Hua Zang ◽  
Qing Chao Gong ◽  
Cun Cun Chen ◽  
Cai Hong Zheng ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Adsorption Capacity ◽  
Petroleum Coke ◽  
Granular Activated Carbon ◽  
Powdered Activated Carbon ◽  
Maximum Adsorption Capacity ◽  
Phenol Removal ◽  
Carbonaceous Materials ◽  
Solution Ph ◽  
Equilibrium Studies

Low cost carbonaceous materials were evaluated for their ability to remove phenol from wastewater. The effects of adsorbents dosage, contact time and maximum adsorption capacity were investigated for granular activated carbon, powdered activated carbon, petroleum coke and multi-walled carbon nanotube (MWNT). Equilibrium studies were conducted in 50mg/L initial phenol concentration, solution pH of 5 and at temperature of 23°C. The results showed the adsorption process was fast and it reached equilibrium in 3 h. Petroleum coke and MWNT had poor adsorption which could reach the removal efficiency of phenol with 43.18% and 36.64% respectively. The granular activated carbon possessed good adsorption ability to phenol with 96.40% at the optimum dosage 5g and optimum time 90min.The powdered activated carbon was an effective adsorbent with a maximum adsorption capacity of 42.32 mg/g.

Coupling of anodic oxidation and adsorption by granular activated carbon for chemical oxygen demand removal from 4,4′-diaminostilbene-2,2′-disulfonic acid wastewater

2010 ◽  
Vol 62 (11) ◽  
pp. 2669-2677 ◽  
Author(s):  
Lizhang Wang ◽  
Yuemin Zhao
Keyword(s):  
Activated Carbon ◽  
Chemical Oxygen Demand ◽  
Residence Time ◽  
Applied Voltage ◽  
Oxygen Demand ◽  
Granular Activated Carbon ◽  
Cod Removal ◽  
Disulfonic Acid ◽  
High Concentration ◽  
Solution Ph

Experiments were performed to reduce chemical oxygen demand (COD) from 4,4′-diaminostilbene-2,2′-disulfonic (DSD) acid manufacturing wastewater using electrochemical oxidation coupled with adsorption by granular activated carbon. The COD removal is affected by the residence time and applied voltage. When the residence time is increased, lower value of COD effluent could be obtained, however, the average current efficiency (ACE) decreased rapidly, and so does the applied voltage. In addition, aeration could effectively enhance COD removal efficiency and protect anodes from corrosion. Furthermore, the acidic condition is beneficial to the rapid decrease of COD and the values of pH effluent are independent of the initial solution pH. The optimization conditions obtained from these experiments are applied voltage of 4.8 V, residence time of 180 min and air–liquid ratio of 4.2 with the COD effluent of about 690 mg L−1. In these cases, the ACE and energy consumption are 388% and 4.144 kW h kg−1 COD, respectively. These perfect results from the experiments illustrate that the combined process is a considerable alternative for the treatment of industrial wastewater containing high concentration of organic pollutants and salinity.

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