Adsorption of Phenol on Red Mud

2013 ◽  
Vol 864-867 ◽  
pp. 1759-1762
Author(s):  
Maroš Soldán ◽  
Lenka Blinová ◽  
Jozef Fiala ◽  
Blanka Galbičková ◽  
Janka Ševčíková ◽  
...  

The objective of this study was to investigate the removal of phenol from aqueous solution by using activated and non-activated red mud in adsorption experiments. The study was carried out as function of red mud dosage and initial phenol concentration. It was found that the maximum removal was obtained at dosage of 0.5 g of red mud and initial concentration of phenol 40 mg/l. Activation has no positive effect on adsorption effectiveness.

2017 ◽  
Vol 76 (6) ◽  
pp. 1466-1473 ◽  
Author(s):  
M. H. Salmani ◽  
M. Mokhtari ◽  
Z. Raeisi ◽  
M. H. Ehrampoush ◽  
H. A. Sadeghian

Wastewater containing pharmaceutical residual components must be treated before being discharged to the environment. This study was conducted to investigate the efficiency of tungsten-carbon nanocomposite in diclofenac removal using design of experiment (DOE). The 27 batch adsorption experiments were done by choosing three effective parameters (pH, adsorbent dose, and initial concentration) at three levels. The nanocomposite was prepared by tungsten oxide and activated carbon powder in a ratio of 1 to 4 mass. The remaining concentration of diclofenac was measured by a spectrometer with adding reagents of 2, 2′-bipyridine, and ferric chloride. Analysis of variance (ANOVA) was applied to determine the main and interaction effects. The equilibrium time for removal process was determined as 30 min. It was observed that the pH had the lowest influence on the removal efficiency of diclofenac. Nanocomposite gave a high removal at low concentration of 5.0 mg/L. The maximum removal for an initial concentration of 5.0 mg/L was 88.0% at contact time of 30 min. The results of ANOVA showed that adsorbent mass was among the most effective variables. Using DOE as an efficient method revealed that tungsten-carbon nanocomposite has high efficiency in the removal of residual diclofenac from the aqueous solution.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Wilson Mwandira ◽  
Kazunori Nakashima ◽  
Satoru Kawasaki ◽  
Allison Arabelo ◽  
Kawawa Banda ◽  
...  

AbstractThe present study investigated biosorption of Pb (II) and Zn (II) using a heavy metal tolerant bacterium Oceanobacillus profundus KBZ 3-2 isolated from a contaminated site. The effects of process parameters such as effect on bacterial growth, pH and initial lead ion concentration were studied. The results showed that the maximum removal percentage for Pb (II) was 97% at an initial concentration of 50 mg/L whereas maximum removal percentage for Zn (II) was at 54% at an initial concentration of 2 mg/L obtained at pH 6 and 30 °C. The isolated bacteria were found to sequester both Pb (II) and Zn (II) in the extracellular polymeric substance (EPS). The EPS facilitates ion exchange and metal chelation-complexation by virtue of the existence of ionizable functional groups such as carboxyl, sulfate, and phosphate present in the protein and polysaccharides. Therefore, the use of indigenous bacteria in the remediation of contaminated water is an eco-friendly way of solving anthropogenic contamination.


2019 ◽  
Vol 14 (4) ◽  
pp. 897-907 ◽  
Author(s):  
Hosseinali Asgharnia ◽  
Hamidreza Nasehinia ◽  
Roohollah Rostami ◽  
Marziah Rahmani ◽  
Seyed Mahmoud Mehdinia

Abstract Phenol and its derivatives are organic pollutants with dangerous effects, such as poisoning, carcinogenicity, mutagenicity, and teratogenicity in humans and other organisms. In this study, the removal of phenol from aqueous solution by adsorption on silica and activated carbon of rice husk was investigated. In this regard, the effects of initial concentration of phenol, pH, dosage of the adsorbents, and contact time on the adsorption of phenol were investigated. The results showed that the maximum removal of phenol by rice husk silica (RHS) and rice husk activated carbon (RHAC) in the initial concentration of 1 mgL−1 phenol, 2 gL−1 adsorbent mass, 120 min contact time, and pH 5 (RHS) or pH 6 (RHAC) were obtained up to 91% and 97.88%, respectively. A significant correlation was also detected between increasing contact times and phenol removal for both adsorbents (p < 0.01). The adsorption process for both of the adsorbents was also more compatible with the Langmuir isotherm. The results of this study showed that RHS and RHAC can be considered as natural and inexpensive adsorbents for water treatment.


2006 ◽  
Vol 41 (1) ◽  
pp. 94-99 ◽  
Author(s):  
Lua'y Zeatoun ◽  
Munjed Al-Sharif ◽  
Abeer Al-Bsoul

Abstract Tar sands were found to remove significant amounts of phenol from aqueous solution in the presence of titania; about 70% at an initial concentration of 10 ppm. Batch sorption experiments showed that phenol uptake was increased with either an increase in initial phenol concentration, percentage of titania in the sorbent or pre-activation temperature. On the other hand, the presence of soft ions such as sodium, Na+, or potassium, K+, or the increase of solution temperature suppressed the uptake of phenol. Physical pre-activation of the tar sands influenced the adsorption process positively. The sorption process appears to be exothermic and relatively fast; the equilibrium isotherm data were well represented by either Langmuir or Freundlich models.


2014 ◽  
Vol 2014 ◽  
pp. 1-8
Author(s):  
Xiao Chen ◽  
Yan Liang ◽  
Xuefei Zhou ◽  
Yanling Zhang

A novel non-photo-dependent semiconductor catalyst (CT) was employed to degrade phenol in the present pilot-scaled study. Effect of operational parameters such as phenol initial concentration, light area, and catalyst loading on phenol degradation, was compared between CT catalyst and the conventional photocatalyst titanium dioxide. CT catalyst excelled titanium dioxide in treating and mineralizing low-level phenol, under both mild UV radiation and thunder conditions of nonphoton. The result suggested that CT catalyst could be applied in circumstances when light is not easily accessible in pollutant-carrying media (e.g., particles, cloudy water, and colored water).


2013 ◽  
Vol 3 (2) ◽  
pp. 119-127 ◽  
Author(s):  
Papita Das Saha ◽  
Jaya Srivastava ◽  
Shamik Chowdhury

The efficacy of seashells as a new adsorbent for removal of phenol from aqueous solutions was studied by performing batch equilibrium tests under different operating parameters such as solution pH, adsorbent dose, initial phenol concentration, and temperature. The phenol removal efficiency remained unaffected when the initial pH of the phenol solution was in the range of 3–8. The amount of phenol adsorbed increased with increasing initial phenol concentration while it decreased with increasing temperature. The adsorption equilibrium data showed excellent fit to the Langmuir isotherm model with maximum monolayer adsorption capacity of 175.27 mg g−1 at pH 4.0, initial phenol concentration = 50 mg L−1, adsorbent dose = 2 g and temperature = 293 K. Analysis of kinetic data showed that the adsorption process followed pseudo-second-order kinetics. Activation energy of the adsorption process, calculated using the Arrhenius equation, was found to be 51.38 kJ mol−1, suggesting that adsorption of phenol onto seashells involved chemical ion-exchange. The numerical value of the thermodynamic parameters (ΔG0, ΔH0 and ΔS0) indicated that adsorption of phenol onto seashells was feasible, spontaneous and endothermic under the examined conditions. The study shows that seashells can be used as an economic adsorbent for removal of phenol from aqueous solution.


2014 ◽  
Vol 15 ◽  
pp. 89-93 ◽  
Author(s):  
R Ulambayar ◽  
J Oyuntsetseg ◽  
A Tsiiregzen ◽  
D Bayaraa

Trivalent chromium (Cr3+) removal from aqueous solution  by electrocoagulation using iron electrodes material was investigated in this paper. Effects of current density, initial concentration of Cr 3+, operating time,  pH, electrode distance, and operating cost have been investigated. At higher current density and solution pH, remarkable removal of Cr3+ was observed. Experiments have been show that the maximum removal percentage of the Cr3+ 99.89 % was at initial concentration 1000mg/L,  current density 9.34mA/cm2 and reaction time 1 hours. Energy consumption was calculated  for Cr3+ removal at different time. The method is observed to be very effective in the removal Cr3+ ion from aqueous solution. Electrocoagulation process need simple equipment, designable any size, use any chemical substances and low operating cost.DOI: http://doi.dx.org/10.5564/mjc.v15i0.330 Mongolian Journal of Chemistry 15 (41), 2014, p89-93


2019 ◽  
Vol 70 (5) ◽  
pp. 1507-1512
Author(s):  
Baker M. Abod ◽  
Ramy Mohamed Jebir Al-Alawy ◽  
Firas Hashim Kamar ◽  
Gheorghe Nechifor

The aim of this study is to use the dry fibers of date palm as low-cost biosorbent for the removal of Cd(II), and Ni(II) ions from aqueous solution by fluidized bed column. The effects of many operating conditions such as superficial velocity, static bed height, and initial concentration on the removal efficiency of metal ions were investigated. FTIR analyses clarified that hydroxyl, amine and carboxyl groups could be very effective for bio-sorption of these heavy metal ions. SEM images showed that dry fibers of date palm have a high porosity and that metal ions can be trapped and sorbed into pores. The results show that a bed height of 6 cm, velocity of 1.1Umf and initial concentration for each heavy metal ions of 50 mg/L are most feasible and give high removal efficiency. The fluidized bed reactor was modeled using ideal plug flow and this model was solved numerically by utilizing the MATLAB software for fitting the measured breakthrough results. The breakthrough curves for metal ions gave the order of bio-sorption capacity as follow: Cd(II)]Ni(II).


2018 ◽  
Vol 6 (1) ◽  
pp. 22-30
Author(s):  
C. Lalhriatpuia ◽  
◽  
Thanhming liana ◽  
K. Vanlaldinpuia

The photocatalytic activity of Nanopillars-TiO2 thin films was assessed in the degradation of Bromophenol blue (BPB) dye from aqueous solution under batch reactor operations. The thin films were characterized by the XRD, SEM and AFM analytical methods. BET specific surface area and pore sizes were also obtained. The XRD data showed anatase phase of TiO2 particles with average particle size of 25.4 and 21.9 nm, for S1 and S2 catalysts respectively. The SEM and AFM images indicated the catalyst composed with Nanosized pillars of TiO2, evenly distributed on the surface of the substrate. The average height of the pillars was found to be 180 and 40 nm respectively for the S1 and S2 catalyst. The BET specific surface area and pore sizes of S1 and S2 catalyst were found to be 5.217 and 1.420 m2/g and 7.77 and 4.16 nm respectively. The photocatalytic degradation of BPB using the UV light was studied at wide range of physico-chemical parametric studies to determine the mechanism of degradation as well as the practical applicability of the technique. The batch reactor operations were conducted at varied pH (pH 4.0 to 10.0), BPB initial concentration (1.0 to 20.0 mg/L) and presence of several interfering ions, i.e., cadmium nitrate, copper sulfate, zinc chloride, sodium chloride, sodium nitrate, sodium nitrite, glycine, oxalic acid and EDTA in the photocatalytic degradation of BPB. The maximum percent removal of BPB was observed at pH 6.0 and a low initial concentration of the pollutant highly favours the photocatalytic degradation using thin films. The presence of several interfering ions suppressed the photocatalytic activity of thin films to some extent. The time dependence photocatalytic degradation of BPB was demonstrated with the pseudo-first-order rate kinetics. Study was further extended with total organic carbon measurement using the TOC (Total Organic Carbon) analysis. This demonstrated an apparent mineralization of BPB from aqueous solutions.


Processes ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 720
Author(s):  
Do Tra Huong ◽  
Nguyen Van Tu ◽  
Duong Thi Tu Anh ◽  
Nguyen Anh Tien ◽  
Tran Thi Kim Ngan ◽  
...  

Fe-Cu materials were synthesized using the chemical plating method from Fe powder and CuSO4 5% solution and then characterized for surface morphology, composition and structure by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD), respectively. The as-synthesized Fe-Cu material was used for removal of phenol from aqueous solution by internal microelectrolysis. The internal electrolysis-induced phenol decomposition was then studied with respect to various parameters such as pH, time, Fe-Cu material weight, phenol concentration and shaking speed. The optimal phenol decomposition (92.7%) was achieved under the conditions of (1) a pH value of phenol solution of 3, (2) 12 h of shaking at the speed of 200 rpm, (3) Fe-Cu material weight of 10 g/L, (4) initial phenol concentration of 100.98 mg/L and (5) at room temperature (25 ± 0.5 °C). The degradation of phenol using Fe-Cu materials obeyed the second-order apparent kinetics equation with a reaction rate constant of k of 0.009 h−1L mg−1. The optimal process was then tested against real coking wastewater samples, resulting in treated wastewater with favorable water indicators. Current findings justify the use of Fe-Cu materials in practical internal electrolysis processes.


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