Removal of Surfactant Cetyldimethylethyl Ammonium Bromide from Water using Adsorption in Combination with a Membrane Pilot Plant

2021 ◽  
Vol 58 (6) ◽  
pp. 475-485
Author(s):  
Muhammad Zahoor ◽  
Sultan Alam ◽  
Muhammad Ali ◽  
Muhammad Sufaid Khan
Keyword(s):  
Pilot Plant ◽  
Entropy Change ◽  
Hybrid Plant ◽  
Ammonium Bromide ◽  
Order Kinetic ◽  
Peanut Shell ◽  
Permeate Flux ◽  
Adsorption Parameters ◽  
Percentage Retention ◽  
C 30

Abstract In this study, a magnetic carbon nanocomposite (MCNC) was prepared using peanut shell biomass as carbon source. The prepared adsorbent was characterised by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), thermogravimetric/differential thermal analysis (TGA/DTA) and BET surface analysis. Batch experiments were carried out to determine the adsorption parameters of cetyl dimethylethyl ammonium bromide (CDEAB) on MCNC. Of the isotherm and kinetics models used, the Langmuir model fitted the equilibrium adsorption data best, while the kinetics data were best explained by the second-order kinetic pseudo-equation. The numerical values of enthalpy change (ΔH8 = 38 kJ mol–1) and Gibb free energy (ΔG8 = 70.95 kJ mol–1, 72.19 kJ mol–1 and 73.32 kJ mol–1 corresponding to 20°C, 30°C and 40 °C, respectively) were positive, while the value of entropy change (ΔS8 = –0.11 kJ mol–1 K–1) indicated an endothermic and non-spontaneous process. After determining the optimal adsorption parameters, the adsorbent was used in a hybrid plant with a membrane pilot plant equipped with ultrafiltration (UF), nanofiltration (NF) and reverse osmosis (RO) membranes. In MCNC/membrane operation, an improvement in permeate flux was observed for the three selected membranes. The percentage retention of UF and NF membranes was also improved by MCNC pre-treatments in hybrid mode.

scholarly journals Activated Ailanthus altissima Sawdust as Adsorbent for Removal of Acid Yellow 29 from Wastewater: Kinetics Approach

Water ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2136
Author(s):  
Najeeb ur Rahman ◽  
Ihsan Ullah ◽  
Sultan Alam ◽  
Muhammad Sufaid Khan ◽  
Luqman Ali Shah ◽  
...  
Keyword(s):  
Adsorption Process ◽  
Entropy Change ◽  
Ailanthus Altissima ◽  
Suitable Model ◽  
Order Kinetic ◽  
X Rays ◽  
Adsorption Parameters ◽  
A Value ◽  
Order Kinetic Model ◽  
C 30

In this study, Ailanthus altissima sawdust was chemically activated and characterized by Scanning Electron Microscopy (SEM), Fourier Transform Infrared (FTIR), Energy Dispersive X rays (EDX), and surface area analyzer. The sawdust was used as an adsorbent for the removal of azo dye; Acid Yellow 29 (AY 29) from wastewater. Different kinetic and equilibrium models were used to calculate the adsorption parameters. Among the applied models, the more suitable model was Freundlich with maximum adsorption capacities of 9.464, 12.798, and 11.46 mg/g at 20 °C, 30 °C, and 40 °C respectively while R2 values close to 1. Moreover, the kinetic data was best fitted in pseudo second order kinetic model with high R2 values approaching to 1. Furthermore, adsorption thermodynamics parameters such as free energy, enthalpy, and entropy were calculated and the adsorption process was found to be exothermic with a value of ∆H° = −9.981 KJ mol−1, spontaneous that was concluded from ΔG° values which were negative (−0.275, −3.422, and −6.171 KJ mol−1 at 20, 30, and 40 °C respectively). A positive entropy change ∆S° with a value of 0.0363 KJ mol−1 indicated the increase disorder during adsorption process. It was concluded that the activated sawdust could be used as a suitable adsorbent for the removal of waste material, especially dyes from polluted waters.

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.

Using of modified-bentonite as low-cost sorbent for removal of methylene blue dye from aqueous solution

2020 ◽  
Vol 27 (2) ◽  
pp. 45-54
Author(s):  
Saraa Muwafaq Ibrahim ◽  
Ziad T. Abd Ali
Keyword(s):  
Aqueous Solution ◽  
Methylene Blue ◽  
Silanol Group ◽  
Infrared Spectrometry ◽  
Blue Dye ◽  
Ammonium Bromide ◽  
Vibration Band ◽  
Order Kinetic ◽  
Methylene Blue Dye ◽  
Modified Bentonite

Batch experiments have been studied to remove methylene blue dye (MB) from aqueous solution using modified bentonite. The modified bentonite was synthesized by replacing exchangeable calcium cations in natural bentonite with cationic surfactant cetyl trimethyl ammonium bromide (CTAB). The characteristics of modified bentonite were studied using different analysis such as Scanning electronic microscopy (SEM), Fourier transform infrared spectrometry (FTIR) and surface area. Where SEM shows the natural bentonite has a porous structure, a rough and uneven appearance with scattered and different block structure sizes, while the modified bentonite surface morphology was smooth and supplemented by a limited number of holes. On other hand, (FTIR) analysis that proved NH group aliphatic and aromatic group of MB and silanol group are responsible for the sorption of contaminate. The organic matter peaks at 2848 and 2930 cm-1 in the spectra of modified bentonite which are sharper than those of the natural bentonite were assigned to the CH2 scissor vibration band and the symmetrical CH3 stretching absorption band, respectively, also the 2930 cm-1 peak is assigned to CH stretching band. The batch study was provided the maximum removal efficiency (99.99 % MB) with a sorption capacity of 129.87 mg/g at specified conditions (100 mg/L, 25℃, pH 11 and 250rpm). The sorption isotherm data fitted well with the Freundlich isotherm model. The kinetic studies were revealed that the sorption follows a pseudo-second-order kinetic model which indicates chemisorption between sorbent and sorbate molecules.

Nano-ZrO2/TiO2 Impregnated Orange Wood Sawdust and Peach Stone Shell Adsorbents for Cr (VI) Removal

2020 ◽  
Vol 16 (7) ◽  
pp. 880-892
Author(s):  
Şerife Parlayıcı ◽  
Kübra Tuna Sezer ◽  
Erol Pehlivan
Keyword(s):  
Contact Time ◽  
Ph Value ◽  
Order Kinetic ◽  
Adsorption Parameters ◽  
Wood Sawdust ◽  
Adsorption Data ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Equilibrium Status

Background: In this work, Cr (VI) adsorption on nano-ZrO2๏TiO2 impregnated orange wood sawdust (Zr๏Ti/OWS) and nano-ZrO2๏TiO2 impregnated peach stone shell (Zr๏Ti/PSS) was investigated by applying different adsorption parameters such as Cr (VI) concentrations, contact time, adsorbent dose, and pH for all adsorbents. Methods: The adsorbents were characterized by SEM and FT-IR. The equilibrium status was achieved after 120 min of contact time and optimum pH value around 2 were determined for Cr (VI) adsorption. Adsorption data in the equilibrium is well-assembled by the Langmuir model during the adsorption process. Results: Langmuir isotherm model showed a maximum adsorption value of OWS: 21.65 mg/g and Zr๏Ti/OWS: 27.25 mg/g. The same isotherm displayed a maximum adsorption value of PSS: 17.64 mg/g, and Zr๏Ti/PSS: 31.15 mg/g. Pseudo-second-order kinetic models (R2=0.99) were found to be the best models for describing the Cr (VI) adsorption reactions. Conclusıon: Thermodynamic parameters such as changes in ΔG°, ΔH°, and ΔS° have been estimated, and the process was found to be spontaneous.

scholarly journals Effective Magnetic MOFs Adsorbent for the Removal of Bisphenol A, Tetracycline, Congo Red and Methylene Blue Pollutions

Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1917
Author(s):  
Guangpu Zhang ◽  
Rong Wo ◽  
Zhe Sun ◽  
Gazi Hao ◽  
Guigao Liu ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Electron Microscope ◽  
Bisphenol A ◽  
Congo Red ◽  
Reduction Process ◽  
Entropy Change ◽  
Potential Candidate ◽  
Order Kinetic ◽  
Adsorption Processes ◽  
Infrared Spectrometer

A magnetic metal−organic frameworks adsorbent (Fe3O4@MIL-53(Al)) was prepared by a typical solvothermal method for the removal of bisphenol A (BPA), tetracycline (TC), congo red (CR), and methylene blue (MB). The prepared Fe3O4@MIL-53(Al) composite adsorbent was well characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), and fourier transform infrared spectrometer (FTIR). The influence of adsorbent quantity, adsorption time, pH and ionic strength on the adsorption of the mentioned pollutants were also studied by a UV/Vis spectrophotometer. The adsorption capacities were found to be 160.9 mg/g for BPA, 47.8 mg/g for TC, 234.4 mg/g for CR, 70.8 mg/g for MB, respectively, which is superior to the other reported adsorbents. The adsorption of BPA, TC, and CR were well-fitted by the Langmuir adsorption isotherm model, while MB followed the Freundlich model, while the adsorption kinetics data of all pollutants followed the pseudo-second-order kinetic models. The thermodynamic values, including the enthalpy change (ΔH°), the Gibbs free energy change (ΔG°), and entropy change (ΔS°), showed that the adsorption processes were spontaneous and exothermic entropy-reduction process for BPA, but spontaneous and endothermic entropy-increasing processes for the others. The Fe3O4@MIL-53(Al) was also found to be easily separated after external magnetic field, can be a potential candidate for future water treatment.

scholarly journals Lignocellulose@ Activated Clay Nanocomposite with Hierarchical Nanostructure Enhancing the Removal of Aqueous Zn(II)

Polymers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1710 ◽  
Author(s):  
Xiaotao Zhang ◽  
Yinan Hao ◽  
Zhangjing Chen ◽  
Yuhong An ◽  
Wanqi Zhang ◽  
...  
Keyword(s):  
Ph Value ◽  
Removal Rate ◽  
Weight Ratio ◽  
Order Kinetic ◽  
Adsorption Parameters ◽  
Hierarchical Nanostructure ◽  
Desorption Temperature ◽  
Desorption Time ◽  
Adsorption Temperature ◽  
Hcl Concentration

A lignocellulose@ activated clay (Ln@AC) nanocomposite with a hierarchical nanostructure was successfully synthesized by the chemical intercalation reaction and applied in the removal of Zn(II) from an aqueous solution. Ln@AC was characterized by N2 adsorption/desorption isotherms and X-Ray Diffraction (XRD), scanning Electron Microscope (SEM), transmission Electron Microscopy (TEM) and Fourier Transform Infrared Spectroscopy (FTIR) analysis, and the results indicate that an intercalated–exfoliated hierarchical nanostructure was formed. The effects of different adsorption parameters on the Zn(II) removal rate (weight ratio of Ln to AC, Ln@AC dosage, initial Zn(II) concentration, pH value, adsorption temperature, and time) were investigated in detail. The equilibrium adsorption capacity reached 315.9 mg/g under optimal conditions (i.e., the weight ratio of Ln to AC of 3:1, Ln@AC dosage of 1 g/L, initial Zn(II) concentration of 600 mg/L, pH value of 6.8, adsorption temperature of 65 °C, and adsorption time of 50 min). The adsorption process was described by the pseudo-second-order kinetic model, Langmuir isotherm model, and the Elovich model. Moreover, Zn(II) could be easily eluted by HCl, and the effects of HCl concentration, desorption temperature, and ultrasonic desorption time on desorbed amount were tested. Desorption studies revealed that with an HCl concentration of 0.25 mol/L, desorption temperature of 70 °C, and ultrasonic desorption time of 20 min, the maximum desorption capacity and efficiency were achieved at 202.5 mg/g and 64.10%, respectively. Regeneration experimental results indicated that the Ln@AC exhibited a certain recyclable regeneration performance. Due to such outstanding features, the novel Ln@AC nanocomposite proved to have great adsorption potential for Zn(II) removal from wastewater, and exhibited an extremely significant amount of adsorbed Zn(II) when compared to conventional adsorbents.

scholarly journals Multi-Component Adsorption of Benzene, Toluene, Ethylbenzene, and Xylene from Aqueous Solutions by Montmorillonite Modified with Tetradecyl Trimethyl Ammonium Bromide

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
H. Nourmoradi ◽  
Mehdi Khiadani ◽  
M. Nikaeen
Keyword(s):  
Experimental Data ◽  
Aqueous Solutions ◽  
Structural Changes ◽  
Freundlich Isotherm ◽  
Isotherm Models ◽  
Ammonium Bromide ◽  
Order Kinetic ◽  
Multicomponent Adsorption ◽  
Benzene Toluene ◽  
Kinetic And Isotherm Models

Multicomponent adsorption of benzene, toluene, ethylbenzene, and xylene (BTEX) was assessed in aqueous solutions by montmorillonite modified with tetradecyl trimethyl ammonium bromide (TTAB-Mt). Batch experiments were conducted to determine the influences of parameters including loading rates of surfactant, contact time, pH, adsorbate concentration, and temperature on the adsorption efficiency. Scanning electron microscope (SEM) and X-ray diffractometer (XRD) were used to determine the adsorbent properties. Results showed that the modification of the adsorbent via the surfactant causes structural changes of the adsorbent. It was found that the optimum adsorption condition achieves with the surfactant loading rate of 200% of the cation exchange capacity (CEC) of the adsorbent for a period of 24 h. The sorption of BTEX by TTAB-Mt was in the order ofB<T<E<X. The experimental data were fitted by many kinetic and isotherm models. The results also showed that the pseudo-second-order kinetic model and Freundlich isotherm model could, respectively, be fitted to the experimental data better than other available kinetic and isotherm models. The thermodynamic study indicated that the sorption of BTEX with TTAB-Mt was achieved spontaneously and the adsorption process was endothermic as well as physical in nature. The regeneration results of the adsorbent also showed that the adsorption capacity of adsorbent after one use was 51% to 70% of original TTAB-Mt.

Adsorption of Chromium (VI) from Aqueous Solution by Agricultural Waste Derived Activated Carbon

2013 ◽  
Vol 726-731 ◽  
pp. 2100-2106 ◽  
Author(s):  
Hua Zhang ◽  
Xue Hong Zhang ◽  
Yi Nian Zhu ◽  
Shou Rui Yuan
Keyword(s):  
Aqueous Solution ◽  
Activated Carbon ◽  
Agricultural Waste ◽  
Order Kinetic ◽  
Chromium Vi ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Grapefruit Peel ◽  
Pseudo Second Order ◽  
C 30

Activated carbon prepared from grapefruit peel, an agricultural solid waste by-product, has been used for the adsorption of Cr(VI) from aqueous solution. The effects of adsorbent dosage, pH and temperature on adsorption of Cr(VI) were investigated. The maximum adsorption yield was obtained at the initial pH of 3. The dynamical data fit very well with the pseudo-second-order kinetic model and the calculated adsorption capacities (23.98, 24.33 and 24.81 mg/g) were in good agreement with experiment results at 20°C, 30°C and 40 °C for the 100 mg/L Cr(VI) solution. The Freundlich model (R2 values were 0.9198-0.9871) fitted adsorption data better than the Langmuir model. The calculated parameters confirmed the favorable adsorption of Cr(VI) on the activated carbon prepared from grapefruit peel.

scholarly journals Comparison of adsorptions by rice hull and Lewatit TP 214 of platinum in chloride solution

2013 ◽  
Vol 78 (6) ◽  
pp. 811-826 ◽  
Author(s):  
M.H. Morcali ◽  
B. Zeytuncu ◽  
O. Yucel
Keyword(s):  
Waste Product ◽  
Second Order ◽  
Attenuated Total Reflection ◽  
Rate Equations ◽  
Rice Hull ◽  
Order Kinetic ◽  
Adsorption Parameters ◽  
Biomass Waste ◽  
Equilibrium Data ◽  
Pseudo Second Order

Rice hull, a biomass waste product, and Lewatit TP 214, a thiosemicarbazide sorbent, were investigated as adsorbents for the adsorption of platinum (IV) ions from synthetically prepared dilute chloroplatinic acid solutions. The rice hull was characterized by Attenuated Total Reflection-Fourier transform infrared spectroscopy (ATR-FTIR). The effects of the different adsorption parameters, sorbent dosage, contact time, temperature and pH of solution on adsorption percentage were studied in detail on a batch sorption. The adsorption equilibrium data were best fitted with the Langmuir isotherm model. The maximum monolayer adsorption capacities, Qmax, at 25?C were found to be 42.02 and 33.22 mg g-1 for the rice hull and Lewatit TP 214, respectively. Thermodynamic calculations using the measured ?H?, ?S? and ?G? values indicate that the adsorption process was spontaneous and exothermic. The pseudo-first-order and pseudo-second-order rate equations were investigated; the adsorption of platinum ions for both sorbents was found to be described by the pseudo-second-order kinetic model. The kinetic rate, k2, using 30 mg sorbent at 25?C was found to be 0.0289 and 0.0039 g min-1 mg-1 for the rice hull and Lewatit TP 214, respectively. The results indicated that the rice hull can be effectively used for the removal of platinum from aqueous solution.

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