scholarly journals Effectiveness of beetroot seeds and H3PO4 activated beetroot seeds for the removal of dyes from aqueous solutions

2017 ◽  
Vol 8 (4) ◽  
pp. 522-531
Author(s):  
A. Machrouhi ◽  
M. Farnane ◽  
A. Elhalil ◽  
R. Elmoubarki ◽  
M. Abdennouri ◽  
...  
Keyword(s):  
Phosphoric Acid ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Solution Ph ◽  
Experimental Isotherm ◽  
Adsorbent Dosage ◽  
Adsorption Capacities ◽  
Monolayer Adsorption ◽  
Order Kinetic Model ◽  
Pseudo Second Order

Abstract Raw beetroot seeds (BS) and H3PO4 activated beetroot seeds (H3PO4-BS) were evaluate for their effectiveness in removing methylene blue (MB) and malachite green (MG) from aqueous solution. BS were carbonized at 500°C for 2 h, and then impregnated with phosphoric acid (phosphoric acid to BS ratio of 1.5 g/g). The impregnated BS were activated in a tubular vertical furnace at 450°C for 2 h. Batch sorption experiments were carried out under various parameters, such as solution pH, adsorbent dosage, contact time, initial dyes concentration and temperature. The experimental results show that the dye sorption was influenced by solution pH and it was greater in the basic range. The sorption yield increases with an increase in the adsorbent dosage. The equilibrium uptake was increased with an increase in the initial dye concentration in solution. Adsorption kinetic data conformed more to the pseudo-second-order kinetic model. The experimental isotherm data were evaluated by Langmuir, Freundlich, Toth and Dubinin–Radushkevich isotherm models. The Langmuir maximum monolayer adsorption capacities were 61.11 and 74.37 mg/g for MB, 51.31 and 213.01 mg/g for MG, respectively in the case of BS and H3PO4-BS. The thermodynamic parameters are also evaluated and discussed.

scholarly journals Dye removal from aqueous solution by raw maize corncob and H3PO4 activated maize corncob

2017 ◽  
Vol 8 (2) ◽  
pp. 214-224 ◽  
Author(s):  
M. Farnane ◽  
H. Tounsadi ◽  
A. Machrouhi ◽  
A. Elhalil ◽  
F. Z. Mahjoubi ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Order Kinetic ◽  
Solution Ph ◽  
Adsorption Performance ◽  
Adsorption Capacities ◽  
Monolayer Adsorption ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Best Fit

AbstractThe focus of this study is the investigation of removal ability of methylene blue (MB) and malachite green (MG) dyes from aqueous solution by raw maize corncob (RMC) and H3PO4 activated maize corncob (AMC). Maize corncobs were carbonized at 500 °C for 2 h, and then impregnated at a phosphoric acid to maize corncob ratio of 2.5 g/g. The impregnated maize corncob was activated in a tubular vertical furnace at 450 °C for 2 h. Samples were characterized by different methods. Adsorption experiments were carried out as a function of solution pH, adsorbent dosage, contact time, initial concentration of dyes and the temperature. Experimental results show that the activation of maize corncob boosts four times the adsorption performance for the selected dyes. The adsorption process is very rapid and was pH dependent with high adsorption capacities in the basic range. The kinetic data were fitted with the pseudo-second-order kinetic model. The best fit of equilibrium data was obtained by the Langmuir model with maximum monolayer adsorption capacities of 75.27 and 271.19 mg/g for MB, 76.42 and 313.63 mg/g for MG, respectively, in the case of RMC and AMC. The temperature did not have much influence on the adsorption performance.

Adsorption of As(V) from Aqueous Solution by the Fe(III)-Impregnated Sorbent Prepared from Sugarcane Bagasse and Applicability of Different Adsorption Models

2013 ◽  
Vol 316-317 ◽  
pp. 509-515
Author(s):  
Hua Zhang ◽  
Xue Hong Zhang ◽  
Yi Nian Zhu ◽  
Mei Na Liang ◽  
Rong Rong Lu
Keyword(s):  
Aqueous Solution ◽  
Sugarcane Bagasse ◽  
Freundlich Isotherm ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Adsorption Models ◽  
Adsorption Capacities ◽  
Monolayer Adsorption ◽  
Order Kinetic Model ◽  
Pseudo Second Order

In this study, a Fe(III)-impregnated sorbent was prepared from sugarcane bagasse and FeCl3 solution via carbonization/activation in a muffle furnace at 500 °C for 4h. Batch experiments were carried out to determine the capacity of the Fe(III)-impregnated sorbent to adsorb As(V) from aqueous solution. The dynamical data fitted very well with the pseudo-second-order kinetic model and the calculated adsorption capacities of 4.8263, 5.2219 and 7.1225 mg/g were equal to the actual values of the experiments at temperatures of 20, 25, and 35 °C, respectively. The experimental data were modeled by Langmuir and Freundlich isotherm models. The Langmuir isotherm with R2 values of 0.9926-0.9968 could yield better fits than the Freundlich isotherm, and the adsorption was endothermic, indicating monolayer adsorption of As(V).Freundlich isotherm, and the adsorption was endothermic, indicating monolayer adsorption of As(V).

Adsorption Characteristics of Phenol in Aqueous Solution by Pinus massoniana Biochar

2013 ◽  
Vol 295-298 ◽  
pp. 1154-1160 ◽  
Author(s):  
Guo Zhi Deng ◽  
Xue Yuan Wang ◽  
Xian Yang Shi ◽  
Qian Qian Hong
Keyword(s):  
Aqueous Solution ◽  
Ph Value ◽  
Pinus Massoniana ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Adsorbent Dosage ◽  
Salt Ions ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The objective of this paper is to investigate the feasibility of phenol adsorption from aqueous solution by Pinus massoniana biochar. Adsorption conditions, including contact time, initial phenol concentration, adsorbent dosage, strength of salt ions and pH, have been investigated by batch experiments. Equilibrium can be reached in 24 h for phenol from 50 to 250 mg• L-1. The optimum pH value for this kind of biochar is 5.0. The amount of phenol adsorbed per unit decreases with the increase in adsorbent dosage. The existence of salt ions makes negligible influence on the equilibrium adsorption capacity. The experimental data is analyzed by the Freundlich and Langmuir isotherm models. Equilibrium data fits well to the Freundlich model. Adsorption kinetics models are deduced and the pseudo-second-order kinetic model provides a good correlation for the adsorbent process. The results show that the Pinus massoniana biochar can be utilized as an effective adsorption material for the removal of phenol from aqueous solution.

scholarly journals Sorption of Cd2+ and Pb2+ on Aragonite Synthesized from Eggshell

2020 ◽  
Vol 12 (3) ◽  
pp. 1174 ◽  
Author(s):  
Lulit Habte ◽  
Natnael Shiferaw ◽  
Mohd Danish Khan ◽  
Thenepalli Thriveni ◽  
Ji Whan Ahn
Keyword(s):  
Experimental Data ◽  
Synthetic Wastewater ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Solution Ph ◽  
Surface Precipitation ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
High Sorption ◽  
Pseudo Second Order

In the present work, waste eggshells were used as a precursor for the synthesis of aragonite crystals through the wet carbonation method. Cadmium (Cd2+) and lead (Pb2+) were removed by the synthesized aragonite from synthetic wastewater. The influence of initial solution pH, contact time, Cd2+ and Pb2+ concentration, and sorbent dosage were evaluated. The major sorption was observed in the first 100 mins and 360 mins for Pb2+and Cd2+ respectively reaching sorption equilibrium at 720 mins (12 hr). The sorption capacity toward Pb2+ was much higher than toward Cd2+. Both heavy metals displayed high sorption capacities at initial pH 6. The pseudo-second-order kinetic model fits well with the experimental data with a higher correlation coefficient R2. Two isotherm models were also evaluated for the best fit with the experimental data obtained. Langmuir isotherm best fits the sorption of the metals on aragonite synthesized from eggshells. X-ray diffraction (XRD) and Scanning electron microscopy (SEM) results of sorbent after sorption showed that the mechanism of sorption was dominated by surface precipitation. Therefore, aragonite crystals synthesized from waste eggshells can be a potential substitute source for the removal of Cd2+ and Pb2+ from contaminated water.

Phosphorus removal from aqueous solution using a novel granular material developed from building waste

2017 ◽  
Vol 75 (6) ◽  
pp. 1500-1511 ◽  
Author(s):  
Shengjiong Yang ◽  
Pengkang Jin ◽  
Xiaochang C. Wang ◽  
Qionghua Zhang ◽  
Xiaotian Chen
Keyword(s):  
Granular Material ◽  
Chemical Precipitation ◽  
Phosphate Removal ◽  
Precipitation Process ◽  
Order Kinetic ◽  
Solution Ph ◽  
Experimental Conditions ◽  
Removal Capacity ◽  
Order Kinetic Model ◽  
Pseudo Second Order

In this study, a granular material (GM) developed from building waste was used for phosphate removal from phosphorus-containing wastewater. Batch experiments were executed to investigate the phosphate removal capacity of this material. The mechanism of removal proved to be a chemical precipitation process. The characteristics of the material and resulting precipitates, the kinetics of the precipitation and Ca2+ liberation processes, and the effects of dosage and pH were investigated. The phosphate precipitation and Ca2+ liberation processes were both well described by a pseudo-second-order kinetic model. A maximum precipitation capacity of 0.51 ± 0.06 mg g−1 and a liberation capacity of 6.79 ± 0.77 mg g−1 were measured under the experimental conditions. The processes reached equilibrium in 60 min. The initial solution pH strongly affected phosphate removal under extreme conditions (pH <4 and pH >10). The precipitates comprised hydroxyapatite and brushite. This novel GM can be considered a promising material for phosphate removal from wastewater.

scholarly journals Simultaneous removal of cationic and anionic dyes from aqueous solution by double functional groups modified bagasse

2020 ◽  
Vol 82 (10) ◽  
pp. 2159-2167
Author(s):  
Ru-yi Zhou ◽  
Jun-xia Yu ◽  
Ru-an Chi
Keyword(s):  
Aqueous Solution ◽  
Functional Groups ◽  
Order Kinetic ◽  
Anionic Dyes ◽  
Adsorption Capacities ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Amine Groups ◽  
Modified Adsorbents ◽  
Zeta Potential Analysis

Abstract Double functional groups modified bagasse (DFMBs), a series of new zwitterionic groups of carboxyl and amine modified adsorbents, were prepared through grafting tetraethylenepentamine (TEPA) onto the pyromellitic dianhydride (PMDA) modified bagasse using the DCC/DMAP method. DFMBs' ability to simultaneously remove basic magenta (BM, cationic dye) and Congo red (CR, anionic dye) from aqueous solution in single and binary dye systems was investigated. FTIR spectra and Zeta potential analysis results showed that PMDA and TEPA were successfully grafted onto the surface of bagasse, and the ratio of the amount of carboxyl groups and amine groups was controlled by the addition of a dosage of TEPA. Adsorption results showed that adsorption capacities of DFMBs for BM decreased while that for CR increased with the increase of the amount of TEPA in both single and binary dye systems, and BM or CR was absorbed on the modified biosorbents was mainly through electrostatic attraction and hydrogen bond. The adsorption for BM and CR could reach equilibrium within 300 min, both processes were fitted well by the pseudo-second-order kinetic model. The cationic and anionic dyes removal experiment in the binary system showed that DMFBs could be chosen as adsorbents to treat wastewater containing different ratios of cationic and anionic dyes.

scholarly journals A Comparative Study on Hexavalent Chromium Adsorption onto Chitosan and Chitosan-Based Composites

Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3427
Author(s):  
Rachid El Kaim Billah ◽  
Moonis Ali Khan ◽  
Young-Kwon Park ◽  
Amira AM ◽  
Hicham Majdoubi ◽  
...  
Keyword(s):  
Sio2 Nanoparticles ◽  
Analysis Data ◽  
Isotherm Models ◽  
Equilibration Time ◽  
Order Kinetic ◽  
Excellent Thermal Stability ◽  
Monolayer Adsorption ◽  
Pseudo Second Order ◽  
Chromium Adsorption ◽  
Ft Ir

Chitosan (Cs)-based composites were developed by incorporating silica (Cs–Si), and both silica and hydroxyapatite (Cs–Si–Hap), comparatively tested to sequester hexavalent (Cr(VI)) ions from water. XRD and FT-IR data affirmed the formation of Cs–Si and Cs–Si–Hap composite. Morphological images exhibits homogeneous Cs–Si surface, decorated with SiO2 nanoparticles, while the Cs–Si–Hap surface was non-homogeneous with microstructures, having SiO2 and Hap nanoparticles. Thermal analysis data revealed excellent thermal stability of the developed composites. Significant influence of pH, adsorbent dose, contact time, temperature, and coexisting anions on Cr(VI) adsorption onto composites was observed. Maximum Cr(VI) uptakes on Cs and developed composites were observed at pH 3. The equilibration time for Cr(VI) adsorption on Cs–Si–Hap was 10 min, comparatively better than Cs and Cs–Si. The adsorption data was fitted to pseudo-second-order kinetic and Langmuir isotherm models with respective maximum monolayer adsorption capacities (qm) of 55.5, 64.4, and 212.8 mg/g for Cs, Cs–Si, and Cs–Si–Hap. Regeneration studies showed that composites could be used for three consecutive cycles without losing their adsorption potential.

scholarly journals Preparation of bio-absorbents by modifying licorice residue via chemical methods and removal of copper ions from wastewater

2021 ◽  
Author(s):  
Xiaochun Yin ◽  
Nadi Zhang ◽  
Meixia Du ◽  
Hai Zhu ◽  
Ting Ke
Keyword(s):  
Adsorption Capacity ◽  
Copper Ions ◽  
Order Kinetic ◽  
Solution Ph ◽  
Chemical Methods ◽  
Simple Strategy ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Surface Active ◽  
Adsorption Desorption

Abstract In this paper, a series of bio-adsorbents (LR-NaOH, LR-Na2CO3 and LR-CA) were successfully prepared by modifying Licorice Residue with NaOH, Na2CO3 and citric acid, which were used as the adsorbents to remove Cu2+ from wastewater. The morphology and structure of bio-adsorbents were characterized by Fourier Transform Infrared, SEM, TG and XRD. Using static adsorption experiments, the effects of the adsorbent dosage, the solution pH, the adsorption time, and the initial Cu2+ concentration on the adsorption performance of the adsorbents were investigated. The results showed that the adsorption process of Cu2+ by the bio-adsorbents can be described by pseudo-second order kinetic model and the Langmuir model. The surface structure of the LR-NaOH, LR-Na2CO3 and LR-CA changed obviously, and the surface-active groups increased. The adsorption capacity of raw LR was 21.56 mg/g, LR-NaOH, LR- Na2CO3 significantly enhanced this value up to 43.65 mg/g, 43.55 mg/g, respectively. After four adsorption-desorption processes, the adsorption capacity of LR-NaOH also maintained about 73%. Therefore, LR-NaOH would be a promising adsorbent for removing Cu2+ from wastewater, and the simple strategy towards preparation of adsorbent from the waste residue can be as a potential approach using in the water treatment.

Equilibrium and Kinetic Studies for the Biosorption of Aqueous Nickel(II) Ions onto the Pseudomonas alcaligenes Biomass

2010 ◽  
Vol 171-172 ◽  
pp. 41-44
Author(s):  
Xiao Cun Xiao ◽  
Gai Xia Fang ◽  
Er Li Zhao ◽  
Lv Bin Zhai ◽  
Jun Shuai Shi
Keyword(s):  
Industrial Wastewater ◽  
Chemical Interaction ◽  
Kinetic Studies ◽  
Synthetic Wastewater ◽  
Order Kinetic ◽  
Adsorption Capacities ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Pseudomonas Alcaligenes ◽  
Batch Biosorption

The objective of this study is to assess the environmentaly friendly Ni(II) adsorption from synthetic wastewater using Pseudomonas alcaligenes biomass (PA-2). The ability of PA-2 to remove the Ni(II) ions was investigated by using batch biosorption procedure. The effects such as pH, dosage of biosorbent, Ni(II) initial concentration and sorbate–sorbent contact time and agitating speed on the adsorption capacities of PA-2 were studied. Biosorption equilibriums were rapidly established in about 60 min and the adsorption kinetics followed the pseudo-second order kinetic model. The maximum Ni(II) adsorption capacity determined from Langmuir isotherm were 82.23 mg/g PA-2 at pH 5.0, at 25±2°C and shaker speed 150 rpm, respectively. The carboxyl , hydroxyl and amino groups of the PA-2 were involved in chemical interaction with the Ni(II) ions depicted by Fourier transform infrared spectroscopic (FTIR) results. The study points to the potential of new use of Pseudomonas alcaligenes biomass as an effective biosorbent for the removal of Ni(II) and from environmental and industrial wastewater.

scholarly journals Adsorption of Cr(VI) ions onto goethite, activated carbon and their composite: kinetic and thermodynamic studies

2020 ◽  
Vol 10 (9) ◽  
Author(s):  
G. B. Adebayo ◽  
H. I. Adegoke ◽  
Sidiq Fauzeeyat
Keyword(s):  
Activated Carbon ◽  
Heavy Metal Contamination ◽  
Stem Bark ◽  
Order Kinetic ◽  
Adsorption Capacities ◽  
Optimum Ph ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Daniellia Oliveri ◽  
Kinetic And Thermodynamic Studies

Abstract Hexavalent chromium was adsorbed from aqueous solution with three prepared and characterized adsorbents, namely goethite (G), activated carbon (AC) and their composite (GAC). The goethite particle was synthesized using the precipitation methods, and activated carbon was prepared from the stem bark of Daniellia oliveri tree and composite in a ratio of 1:5 goethite–activated carbon. The adsorption capacities of G, AC and GAC for Cr(VI) are 6.627, 5.455 and 6.354 mg/g with 0.02 g adsorbent within contact time of 60, 180 and 30 min for G, AC and GAC, respectively, for Cr(VI) adsorption at optimum pH of 3. The isotherm studied was best explained by Langmuir adsorption isotherm and fitted with the pseudo-second-order kinetic model. Desorption studies showed that 1.0 M HNO3 was a better desorbing agent than 0.1 M HNO3, 0.1 M HCl and 1.0 M HCl. Chromium was most desorbed (94.60% in Cr//G using 1 M HNO3). The result obtained revealed that goethite and activated carbon produced are favourable adsorbents and the composite of the two adsorbents gives a more favourable, economical and affordable adsorbent for the clean-up of heavy metal contamination.

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