scholarly journals Removal of organic pollutants from produced water by batch adsorption treatment

2021 ◽  
Author(s):  
Eman Hashim Khader ◽  
Thamer Jassim Mohammed ◽  
Nourollah Mirghaffari ◽  
Ali Dawood Salman ◽  
Tatjána Juzsakova ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Produced Water ◽  
Oxygen Demand ◽  
Powdered Activated Carbon ◽  
Pollutant Removal ◽  
Operating Conditions ◽  
Isotherm Models ◽  
Batch Adsorption ◽  
Order Kinetic ◽  
Zeolite X

AbstractThis paper studied the adsorption of chemical oxygen demand (COD), oil and turbidity of the produced water (PW) which accompanies the production and reconnaissance of oil after treating utilizing powdered activated carbon (PAC), clinoptilolite natural zeolite (CNZ) and synthetic zeolite type X (XSZ). Moreover, the paper deals with the comparison of pollutant removal over different adsorbents. Adsorption was executed in a batch adsorption system. The effects of adsorbent dosage, time, pH, oil concentration and temperature were studied in order to find the best operating conditions. The adsorption isotherm models of Langmuir, Freundlich and Temkin were investigated. Using pseudo-first-order and pseudo-second-order kinetic models, the kinetics of oil sorption and the shift in COD content on PAC and CNZ were investigated. At a PAC adsorbent dose of 0.25 g/100 mL, maximum oil removal efficiencies (99.57, 95.87 and 99.84 percent), COD and total petroleum hydrocarbon (TPH) were identified. Moreover, when zeolite X was used at a concentration of 0.25 g/100 mL, the highest turbidity removal efficiency (99.97%) was achieved. It is not dissimilar to what you would get with PAC (99.65 percent). In comparison with zeolites, the findings showed that adsorption over PAC is the most powerful method for removing organic contaminants from PW. In addition, recycling of the consumed adsorbents was carried out in this study to see whether the adsorbents could be reused. Chemical and thermal treatment will effectively regenerate and reuse powdered activated carbon and zeolites that have been eaten. Graphic abstract

scholarly journals Removal of Organic Pollutantsfrom Produced Water by Batch Adsorption Treatment

2021 ◽  
Author(s):  
Eman Hashim Khader ◽  
Thamer Jassim Mohammed ◽  
Nourollah Mirghaffari ◽  
ali Dawood Salman ◽  
Tatjána Juzsakova ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Produced Water ◽  
Oxygen Demand ◽  
Powdered Activated Carbon ◽  
Pollutant Removal ◽  
Isotherm Models ◽  
Batch Adsorption ◽  
Zeolite X ◽  
Operational Conditions ◽  
Sorption System

Abstract This paper investigates the adsorption of oil, chemical oxygen demand (COD) and turbidity of the produced water (PW) which accompanies the oil exploration and production after treatment by using powdered activated carbon (PAC), clinoptilolite natural zeolite (CNZ) and synthetic zeolite type X (XSZ). Moreover, the paper deals with the comparison of pollutant removal over different adsorbents. Sorption was carried out in batch sorption system. The operating factors including adsorbent dosage, time, pH, oil concentration and temperature were investigated to determine the optimum operational conditions. Three adsorption isotherm models (Langmuir, Freundlich and Temkin models) were applied. The kinetics of the oil sorption and the change in COD content over on PAC and CNZ were studied by using pseudo-first order and pseudo-second order kinetics models. Maximum oil removal efficiencies (99.57, 95.87 and 99.84%), COD and total petroleum hydrocarbon (TPH), respectively were found at PAC adsorbent dose of 0.25 g/100 mL. However, maximum turbidity removal efficiency (99.97%) was obtained when zeolite X was used at 0.25g/100 mL concentration. It is not very different from that obtained over PAC (99.65%). The results proved that adsorption over PAC is most effective compared to zeolites in the removal of organic pollutants from PW. Also, regeneration of the consumed adsorbents was carried out in this work to find out the possibility of reusing the adsorbents. The consumed powdered activated carbon and zeolites can be effectively regenerated and reused by chemical treatment and thermal treatment respectively.

scholarly journals Adsorption and Photocatalytic Mineralization of Bromophenol Blue Dye with TiO2 Modified with Clinoptilolite/Activated Carbon

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 7
Author(s):  
Emmanuel Kweinor Tetteh ◽  
Sudesh Rathilal
Keyword(s):  
Activated Carbon ◽  
Photocatalytic Degradation ◽  
Oxygen Demand ◽  
Freundlich Isotherm ◽  
Reaction Rate Constant ◽  
Coefficient Of Determination ◽  
Bromophenol Blue ◽  
Blue Dye ◽  
Order Kinetic ◽  
Co Precipitation

This study presents a hybridized photocatalyst with adsorbate as a promising nanocomposite for photoremediation of wastewater. Photocatalytic degradation of bromophenol blue (BPB) in aqueous solution under UV-irradiation of wavelength 400 nm was carried out with TiO2 doped with activated carbon (A) and clinoptilolite (Z) via the co-precipitation technique. The physiochemical properties of the nanocomposite (A–TiO2 and Z–TiO2) and TiO2 were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier-transform infrared (FTIR) spectroscopy. Results of the nanocomposite (A–TiO2 and Z–TiO2) efficiency was compared to that with the TiO2, which demonstrated their adsorption and synergistic effect for the removal of chemical oxygen demand (COD) and color from the wastewater. At an optimal load of 4 g, the photocatalytic degradation activity (Z–TiO2 > A–TiO2 > TiO2) was found favorably by the second-order kinetic model. Consequently, the Langmuir adsorption isotherms favored the nanocomposites (Z–TiO2 > A–TiO2), whereas that of the TiO2 fitted very well on the Freundlich isotherm approach. Z–TiO2 evidently exhibited a high photocatalytic efficacy of decomposition over 80% of BPB (COD) at reaction rate constant (k) and coefficient of determination (R2) values of 5.63 × 10−4 min−1 and 0.989, respectively.

scholarly journals Performance of Iron-Functionalized Activated Carbon Catalysts (Fe/AC-f) on CWPO Wastewater Treatment

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 337
Author(s):  
Sara Mesa Medina ◽  
Ana Rey ◽  
Carlos Durán-Valle ◽  
Ana Bahamonde ◽  
Marisol Faraldos
Keyword(s):  
Wastewater Treatment ◽  
Activated Carbon ◽  
Landfill Leachate ◽  
Surface Composition ◽  
Treatment Plant ◽  
Reaction Medium ◽  
Pollutant Removal ◽  
Operating Conditions ◽  
Water Matrix ◽  
The Stability

Two commercial activated carbon were functionalized with nitric acid, sulfuric acid, and ethylenediamine to induce the modification of their surface functional groups and facilitate the stability of corresponding AC-supported iron catalysts (Fe/AC-f). Synthetized Fe/AC-f catalysts were characterized to determine bulk and surface composition (elemental analysis, emission spectroscopy, XPS), textural (N2 isotherms), and structural characteristics (XRD). All the Fe/AC-f catalysts were evaluated in the degradation of phenol in ultrapure water matrix by catalytic wet peroxide oxidation (CWPO). Complete pollutant removal at short reaction times (30–60 min) and high TOC reduction (XTOC = 80 % at ≤ 120 min) were always achieved at the conditions tested (500 mg·L−1 catalyst loading, 100 mg·L−1 phenol concentration, stoichiometric H2O2 dose, pH 3, 50 °C and 200 rpm), improving the results found with bare activated carbon supports. The lability of the interactions of iron with functionalized carbon support jeopardizes the stability of some catalysts. This fact could be associated to modifications of the induced surface chemistry after functionalization as a consequence of the iron immobilization procedure. The reusability was demonstrated by four consecutive CWPO cycles where the activity decreased from 1st to 3rd, to become recovered in the 4th run. Fe/AC-f catalysts were applied to treat two real water matrices: the effluent of a wastewater treatment plant with a membrane biological reactor (WWTP-MBR) and a landfill leachate, opening the opportunity to extend the use of these Fe/AC-f catalysts for complex wastewater matrices remediation. The degradation of phenol spiked WWTP-MBR effluent by CWPO using Fe/AC-f catalysts revealed pH of the reaction medium as a critical parameter to obtain complete elimination of the pollutant, only reached at pH 3. On the contrary, significant TOC removal, naturally found in complex landfill leachate, was obtained at natural pH 9 and half stoichiometric H2O2 dose. This highlights the importance of the water matrix in the optimization of the CWPO operating conditions.

scholarly journals Using one filter stage of unsaturated/saturated vertical flow filters for nitrogen removal and footprint reduction of constructed wetlands

2017 ◽  
Vol 76 (1) ◽  
pp. 124-133 ◽  
Author(s):  
Ania Morvannou ◽  
Stéphane Troesch ◽  
Dirk Esser ◽  
Nicolas Forquet ◽  
Alain Petitjean ◽  
...  
Keyword(s):  
Constructed Wetlands ◽  
Oxygen Demand ◽  
Pollutant Removal ◽  
Operating Conditions ◽  
Vertical Flow ◽  
Saturated Layer ◽  
Recirculation Rate ◽  
Total Filtration ◽  
Filtration Area ◽  
Stage System

French vertical flow constructed wetlands (VFCW) treating raw wastewater have been developed successfully over the last 30 years. Nevertheless, the two-stage VFCWs require a total filtration area of 2–2.5 m2/P.E. Therefore, implementing a one-stage system in which treatment performances reach standard requirements is of interest. Biho-Filter® is one of the solutions developed in France by Epur Nature. Biho-Filter® is a vertical flow system with an unsaturated layer at the top and a saturated layer at the bottom. The aim of this study was to assess this new configuration and to optimize its design and operating conditions. The hydraulic functioning and pollutant removal efficiency of three different Biho-Filter® plants commissioned between 2011 and 2012 were studied. Outlet concentrations of the most efficient Biho-Filter® configuration are 70 mg/L, 15 mg/L, 15 mg/L and 25 mg/L for chemical oxygen demand (COD), 5-day biological oxygen demand (BOD5), total suspended solids (TSS) and total Kjeldahl nitrogen (TKN), respectively. Up to 60% of total nitrogen is removed. Nitrification efficiency is mainly influenced by the height of the unsaturated zone and the recirculation rate. The optimum recirculation rate was found to be 100%. Denitrification in the saturated zone works at best with an influent COD/NO3-N ratio at the inflet of this zone larger than 2 and a hydraulic retention time longer than 0.75 days.

scholarly journals Effects of selection and compiling strategy of substrates in column-type vertical-flow constructed wetlands on the treatment of synthetic landfill leachate containing bisphenol A

2021 ◽  
Author(s):  
Rajani Ghaju Shrestha ◽  
Daisuke Inoue ◽  
Michihiko Ike
Keyword(s):  
Activated Carbon ◽  
Bisphenol A ◽  
Landfill Leachate ◽  
Low Cost ◽  
Oxygen Demand ◽  
Ammonium Nitrogen ◽  
Pollutant Removal ◽  
Vertical Flow ◽  
Batch Mode ◽  
Synthetic Leachate

Abstract A constructed wetland (CW) is a low-cost, eco-friendly, easy-to-maintain, and widely applicable technology for treating various pollutants in the waste landfill leachate. This study determined the effects of the selection and compiling strategy of substrates used in CWs on the treatment performance of a synthetic leachate containing bisphenol A (BPA) as a representative recalcitrant pollutant. We operated five types of lab-scale vertical-flow CWs using only gravel (CW1), a sandwich of gravel with activated carbon (CW2) or brick crumbs (CW3), and two-stage hybrid CWs using gravel in one column and activated carbon (CW4) or brick crumbs (CW5) in another to treat synthetic leachate containing BPA in a 7-d sequential batch mode for 5 weeks. CWs using activated carbon (CW2 and CW4) effectively removed ammonium nitrogen (NH4-N) (99–100%), chemical oxygen demand (COD) (93–100%), and BPA (100%), indicating that the high adsorption capacity of activated carbon was the main mechanism involved in their removal. CW5 also exhibited higher pollutant removal efficiencies (NH4-N: 94–99%, COD: 89–98%, BPA: 89–100%) than single-column CWs (CW1 and CW3) (NH4-N: 76–100%, COD: 84–100%, BPA: 51–100%). This indicates the importance of the compiling strategy along with the selection of an appropriate substrate to improve the pollutant removal capability of CWs.

Nanoparticle Fe3O4 magnetized activated carbon from Armeniaca sibirica shell for the adsorption of Hg(II) ions

BioResources ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. 6100-6120
Author(s):  
Yinan Hao ◽  
Yanfei Pan ◽  
Qingwei Du ◽  
Xudong Li ◽  
Ximing Wang
Keyword(s):  
Activated Carbon ◽  
Adsorption Capacity ◽  
Ph Value ◽  
Removal Rate ◽  
Freundlich Isotherm ◽  
Entropy Change ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Adsorption Parameters ◽  
Initial Concentration

Armeniaca sibirica shell activated carbon (ASSAC) magnetized by nanoparticle Fe3O4 prepared from Armeniaca sibirica shell was investigated to determine its adsorption for Hg2+ from wastewater. Fe3O4/ASSAC was characterized using XRD (X-ray diffraction), FTIR (Fourier transform infrared spectroscopy), SEM (scanning electron microscopy), and BET (Brunauer–Emmett–Teller). Optimum adsorption parameters were determined based on the initial concentration of Hg2+, reaction time, reaction temperature, and pH value in adsorption studies. The experiment results demonstrated that the specific surface area of ASSAC decreased after magnetization; however the adsorption capacity and removal rate of Hg2+ increased 0.656 mg/g and 0.630%, respectively. When the initial concentration of Hg2+ solution was 250 mg/L and the pH value was 2, the adsorption time was 180 min and the temperature was 30 °C, and with the Fe3O4/ASSAC at 0.05 g, the adsorption reaching 97.1 mg/g, and the removal efficiency was 99.6%. The adsorption capacity of Fe3O4/ASSAC to Hg2+ was in accord with Freundlich isotherm models, and a pseudo-second-order kinetic equation was used to fit the adsorption best. The Gibbs free energy ΔGo < 0，enthalpy change ΔHo < 0, and entropy change ΔSo < 0 which manifested the adsorption was a spontaneous and exothermic process.

scholarly journals Removal of Cu(II) from Aqueous Solutions Using Amine-Doped Polyacrylonitrile Fibers

2020 ◽  
Vol 10 (5) ◽  
pp. 1738
Author(s):  
Kay Thwe Aung ◽  
Seung-Hee Hong ◽  
Seong-Jik Park ◽  
Chang-Gu Lee
Keyword(s):  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Isotherm Models ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Equilibrium Studies ◽  
Naoh Solution ◽  
Surface Modified ◽  
Pan Fibers

Polyacrylonitrile (PAN) fibers were prepared via electrospinning and were modified with diethylenetriamine (DETA) to fabricate surface-modified PAN fibers. The surface-modified PAN fibers were used to evaluate their adsorption capacity for the removal of Cu(II) from aqueous solutions. Batch adsorption experiments were performed to examine the effects of the modification process, initial concentration, initial pH, and adsorbent dose on the adsorption of Cu(II). Kinetic analysis revealed that the experimental data fitted the pseudo-second-order kinetic model better than the pseudo-first-order model. Adsorption equilibrium studies were conducted using the Freundlich and Langmuir isotherm models, and the findings indicated that the PAN fibers modified with 85% DETA presented the highest adsorption capacity for Cu(II) of all analyzed samples. Moreover, the results revealed that the Freundlich model was more appropriate than the Langmuir one for describing the adsorption of Cu(II) onto the modified fibers at various initial Cu(II) concentrations. The maximum adsorption capacity was determined to be 87.77 mg/g at pH 4, and the percent removal of Cu(II) increased as the amount of adsorbent increased. Furthermore, the surface-modified PAN fibers could be easily regenerated using NaOH solution. Therefore, surface-modified PAN fibers could be used as adsorbents for the removal of Cu(II) from aqueous solutions.

Adsorption performance of powdered activated carbon-ultrafiltration systems

2001 ◽  
Vol 1 (5-6) ◽  
pp. 13-19 ◽  
Author(s):  
C. Campos ◽  
I. Baudin ◽  
J.M. Lainé
Keyword(s):  
Activated Carbon ◽  
Adsorption Process ◽  
Carbon Particle ◽  
Drinking Water Treatment ◽  
Powdered Activated Carbon ◽  
Operating Conditions ◽  
Adsorption Model ◽  
Filtration Time ◽  
Adsorption Removal ◽  
Carbon Performance

The use of powdered activated carbon in combination with ultrafiltration membranes is attracting increasing interest for the removal of organic compounds in drinking water treatment. The overall adsorption efficiency of this hybrid membrane process strongly depends on the reactor configuration and its operating conditions. Identification of the operating conditions yielding optimum carbon performance can be facilitated by the use of mathematical models describing the adsorption process. In this study, the effect of various designs and operating parameters on the efficiency of the adsorption process is discussed using an adsorption model previously developed and verified by the authors. This discussion includes the effect of filtration time, membrane reactor volume, carbon dosing procedure, carbon dose and carbon particle size on the adsorption removal of two selected micropollutants and dissolved organic matter.

scholarly journals Adsorption of Hexavalent Chromium from Aqueous Solution Using Chemically Activated Carbon Prepared from Locally Available Waste of Bamboo (Oxytenanthera abyssinica)

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Tamirat Dula ◽  
Khalid Siraj ◽  
Shimeles Addisu Kitte
Keyword(s):  
Activated Carbon ◽  
Hexavalent Chromium ◽  
Freundlich Isotherm ◽  
Kinetic Studies ◽  
Batch Adsorption ◽  
Koh Activation ◽  
Order Kinetic ◽  
Oxytenanthera Abyssinica ◽  
Equilibrium Data ◽  
Order Kinetic Model

This study reports on the adsorption of Hexavalent Chromium from aqueous solutions using activated carbon prepared from bamboo (Oxytenanthera abyssinica) waste by KOH activation heating in an electrical furnace at 1073 K for 3 hrs. Batch adsorption experiments were also carried out as a function of pH, contact time, initial concentration of the adsorbate, adsorbent dosage, and temperature of the solution. Kinetic studies of the data showed that the adsorption follows the pseudo-second-order kinetic model. Thermodynamic parameters showed that adsorption on the surface of BWAC was feasible, spontaneous in nature, and exothermic between temperatures of 298 and 318 K. The equilibrium data better fitted the Freundlich isotherm model for studying the adsorption behavior of Hexavalent Chromium by BWAC. IR spectrum for loaded and unloaded BWAC was obtained using FT-IR spectrophotometer. Adsorption efficiency and capacity of Hexavalent Chromium were found to be 98.28% at pH 2 and 59.23 mg/g at 300 K.

Electrochemical removal of carbamazepine in water with Ti/PbO2 cylindrical mesh anode

2015 ◽  
Vol 73 (5) ◽  
pp. 1155-1165 ◽  
Author(s):  
J. D. García-Espinoza ◽  
P. Gortáres-Moroyoqui ◽  
M. T. Orta-Ledesma ◽  
P. Drogui ◽  
P. Mijaylova-Nacheva
Keyword(s):  
Supporting Electrolyte ◽  
Oxygen Demand ◽  
Electrochemical Reactor ◽  
Operating Conditions ◽  
Current Intensity ◽  
Oxygen Flux ◽  
Order Kinetic ◽  
Electrolysis Time ◽  
Direct Oxidation

Carbamazepine (CBZ) is one of the most frequently detected organic compounds in the aquatic environment. Due to its bio-persistence and toxicity for humans and the environment its removal has become an important issue. The performance of the electrochemical oxidation process and in situ production of reactive oxygen species (ROS), such as O3 and H2O2, for CBZ removal have been studied using Ti/PbO2 cylindrical mesh anode in the presence of Na2SO4 as supporting electrolyte in a batch electrochemical reactor. In this integrated process, direct oxidation at anode and indirect oxidation by in situ electrogenerated ROS can occur simultaneously. The effect of several factors such as electrolysis time, current intensity, initial pH and oxygen flux was investigated by means of an experimental design methodology, using a 24 factorial matrix. CBZ removal of 83.93% was obtained and the most influential parameters turned out to be electrolysis time, current intensity and oxygen flux. Later, the optimal experimental values for CBZ degradation were obtained by means of a central composite design. The best operating conditions, analyzed by Design Expert® software, are the following: 110 min of electrolysis at 3.0 A, pH = 7.05 and 2.8 L O2/min. Under these optimal conditions, the model prediction (82.44%) fits very well with the experimental response (83.90 ± 0.8%). Furthermore, chemical oxygen demand decrease was quantified. Our results illustrated significant removal efficiency for the CBZ in optimized condition with second order kinetic reaction.

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