scholarly journals Evaluation of NH 4 + Adsorption Capacity in Water of Coffee Husk-Derived Biochar at Different Pyrolysis Temperatures

2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Nguyen Van Phuong ◽  
Nguyen Khanh Hoang ◽  
Le Van Luan ◽  
L. V. Tan
Keyword(s):  
Adsorption Capacity ◽  
Adsorption Equilibrium ◽  
Water Environment ◽  
Exchange Capacity ◽  
Order Kinetic ◽  
Coffee Husk ◽  
Removal Capacity ◽  
Equilibrium And Kinetics ◽  
Order Kinetic Model ◽  
Adsorption Equilibrium And Kinetics

Ammonium NH 4 + is a pollutant that can be harmful to the water environment. The purpose of this study is to access NH 4 + removal capacity from water by coffee husk-derived biochar. The properties of biochar prepared at different temperatures (300, 450, and 600°C) were determined including TOC, and pH , pH pzc , functional groups of H+/OH−, cation-exchange capacity (CEC), and the characteristics of groups of organic matter (FT-IR spectrum) were identified and evaluated. The trend of NH 4 + adsorption equilibrium and kinetics of biochar have been studied. The experimental design of adsorption equilibrium was carried out by exposing biochar to a NH 4 + solution at different concentrations, ranging from 0 to 50 mg NH 4 + / L for 12 hours. Kinetic surveys were carried out when biochar was exposed to a solution containing 8.3 mg NH 4 + / L for a varying length of time. The results showed that Langmuir and Freundlich models and the pseudo-second-order kinetic model are suitable to explain the NH 4 + adsorption equilibrium and kinetics on the biochar forms derived from coffee husk. Biochar derived from coffee husk prepared at lower pyrolysis temperature has a higher adsorption capacity. The results suggest that the biochar could be used as an adsorbent ammonium from water.

scholarly journals Comparison of Adsorptive Removal of Total Nitrogen (T-N) and Total Phosphorous (T-P) in Aqueous Solution using Granular Activated Charcoal (GAC)

2013 ◽  
Vol 9 (1) ◽  
pp. 1822-1836
Author(s):  
Keon Sang Ryoo ◽  
Jong-Ha Choi ◽  
Yong Pyo Hong
Keyword(s):  
Aqueous Solution ◽  
Kinetic Model ◽  
Adsorption Capacity ◽  
Total Nitrogen ◽  
Activated Charcoal ◽  
Adsorption Equilibrium ◽  
Order Kinetic ◽  
Total Phosphorous ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The present study is to explore the possibility of utilizing granular activated charcoal (GAC) for the removal of total phosphorous (T-P) and total nitrogen (T-N) in aqueous solution. Batch adsorption studies were carried out to determine the influences of various factors like initial concentration, contact time and temperature. The adsorption data showed that GAC has a similar adsorption capacity for both T-N and T-P. The adsorption degree of T-N and T-P on GAC was highly concentration dependent. It was found that the adsorption capacity of GAC is quite favorable at a low concentration. At concentrations of 1.0 mg L-1 of T-P and 2.0 mg L-1 of T-N, approximately 97 % of adsorption was achieved by GAC. The equilibrium data were fitted well to the Langmuir isotherm model. The pseudo-second-order kinetic model appeared to be the better-fitting model because it has higher R2 compared with the pseudo-first-order and intra-particle kinetic model. The theoretical adsorption equilibrium qe,cal from pseudo-second-order kinetic model were relatively similar to the experimental adsorption equilibrium qe,exp. To evaluate the effect of thermodynamic parameters at different temperatures, the change in free energy ΔG, the enthalpy ΔH and the entropy ΔS were estimated. Except for adsorption of T-P at 278 K, the ΔG values obtained were all negative at the investigated temperatures. It indicates that the present adsorption system occurs spontaneously. The adsorption process of T-N by GAC was exothermic in nature, whereas T-P showed endothermic behavior. In addition, the positive values of ΔS imply that there was the increase in the randomness of adsorption of T-N and T-P at GAC-solution interface.  

scholarly journals High Selectivity and Reusability of Biomass-Based Adsorbent for Chloramphenicol Removal

Nanomaterials ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 2950
Author(s):  
Weinan Xing ◽  
Qi Liu ◽  
Jingyi Wang ◽  
Siye Xia ◽  
Li Ma ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Solution Structure ◽  
Low Cost ◽  
Water Environment ◽  
Significant Loss ◽  
Order Kinetic ◽  
Solution Ph ◽  
Suitable Material ◽  
Order Kinetic Model ◽  
Pseudo Second Order

Recently, biomass-based materials have attracted increasing attention because of their advantages of low cost, environment-friendly and nonpollution. Herein, the feasibility of using corn stalk biomass fiber (CF) and Fe3O4 embedded chitosan (CS) as a novel biomass-based adsorbent (CFS) to remove chloramphenicol (CAPC) from aqueous solution. Structure of CFS was characterized by using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Brunauer–Emmett–Teller (BET), scanning electron microscopy (SEM) and zeta potential techniques. The effects of solution pH, adsorption time and ion strength on the adsorption capacity were examined. Adsorption isotherms obtained from batch experiments were better fitted by Langmuir model compared with Freundlich model, Dubinin–Radushkevich model and Temkin model. Adsorption kinetic data matched well to the pseudo-second order kinetic model. CAPC adsorption was endothermic, spontaneous, and entropy-increasing nature on CFS. In addition, the CFS could be separated by an external magnetic field, recycled, and reused without any significant loss in the adsorption capacity of CAPC. Based on these excellent performances, there is potential that CFS can be considered as a proficient and economically suitable material for the CAPC removal from the water environment.

Adsorption Equilibrium and Kinetics of CO2 and H2O on Activated Carbon

2012 ◽  
Vol 27 (2) ◽  
pp. 139-145 ◽  
Author(s):  
Dong XU ◽  
Jun ZHANG ◽  
Gang LI ◽  
Penny XIAO ◽  
Paul WEBLEY ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Adsorption Equilibrium ◽  
Equilibrium And Kinetics ◽  
Adsorption Equilibrium And Kinetics ◽  
Kinetics Of

scholarly journals Factors influencing the adsorption and photocatalysis of direct red 80 in the presence of a TiO2: Equilibrium and kinetics modeling

2021 ◽  
pp. 174751982198996
Author(s):  
Moussa Abbas
Keyword(s):  
Elimination Rate ◽  
Threshold Value ◽  
Heterogeneous Photocatalysis ◽  
Order Kinetic ◽  
Batch Mode ◽  
Adsorption Capacities ◽  
Initial Ph ◽  
Equilibrium And Kinetics ◽  
Order Kinetic Model ◽  
Charge Point

Among the different photocatalysts, TiO2 ( Eg = 3.1 eV, zero charge point (pHpzc = 6.3), and surface = 55 m2/g) is currently the most efficient and the most studied semiconductor due to its strong photocatalytic activity, non-toxicity, and chemical stability. The elimination of DR-80 on TiO2 is studied by adsorption in batch mode and by application of heterogeneous photocatalysis onto TiO2 under UV irradiation. The effects of contact time (0–60 min), initial pH (3–11), dose of the adsorbent (0.5–3 g L−1), and DR-80 concentration (40–60 mg L−1) on the adsorption of DR-80 by TiO2 are studied for optimization of these parameters. The kinetic parameters, rate constants, and equilibrium adsorption capacities are calculated and discussed for each applied theoretical model. The adsorption of DR-80 is well described by the pseudo-first-order kinetic model. The fitting of the adsorption isotherms shows that the models of Langmuir and Temkin offering a better fit and an adsorption 64.102 mg/g at 25 °C of DR-80 are eliminated. The results showed that the photocatalytic efficiency strongly depends on the pH while the initial rate of photodegradation is proportional to the catalyst dose, and becomes almost constant above a threshold value. It was found that the photodegradation is favored at low DR-80 concentrations in accordance with the Langmuir–Hinshelwood model with the constants Kad = 6.5274 L/mg and KL–H = 0.17818 mg L−1 min. However, the adsorption is improved for high DR-80 concentrations. It is found that the degradation depends on both the temperature and the pH with a high elimination rate at high temperature. The photocatalyst TiO2 has a better activity for the degradation of DR-80, compared to some commercial catalysts that have been described in the literature.

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 Insights into Starch Coated Nanozero Valent Iron-Graphene Composite for Cr(VI) Removal from Aqueous Medium

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Prasanna Kumarathilaka ◽  
Vimukthi Jayaweera ◽  
Hasintha Wijesekara ◽  
I. R. M. Kottegoda ◽  
S. R. D. Rosa ◽  
...  
Keyword(s):  
Point Of Zero Charge ◽  
Inert Material ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Graphene Composite ◽  
Removal Capacity ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
First Time

Embedding nanoparticles into an inert material like graphene is a viable option since hybrid materials are more capable than those based on pure nanoparticulates for the removal of toxic pollutants. This study reports for the first time on Cr(VI) removal capacity of novel starch stabilized nanozero valent iron-graphene composite (NZVI-Gn) under different pHs, contact time, and initial concentrations. Starch coated NZVI-Gn composite was developed through borohydrate reduction method. The structure and surface of the composite were characterized by scanning electron microscopy (SEM), X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), and point of zero charge (pHpzc). The surface area and pHpzc of NZVI-Gn composite were reported as 525 m2 g−1 and 8.5, respectively. Highest Cr(VI) removal was achieved at pH 3, whereas 67.3% was removed within first few minutes and reached its equilibrium within 20 min obeying pseudo-second-order kinetic model, suggesting chemisorption as the rate limiting process. The partitioning of Cr(VI) at equilibrium is perfectly matched with Langmuir isotherm and maximum adsorption capacity of the NZVI-Gn composite is 143.28 mg g−1. Overall, these findings indicated that NZVI-Gn composite could be utilized as an efficient and magnetically separable adsorbent for removal of Cr(VI).

scholarly journals Optimization of cadmium(II) adsorption onto modified and unmodified lignocellulosics (rice husk and egussi peeling)

2015 ◽  
Vol 5 (1) ◽  
pp. 45
Author(s):  
Tchuifon Tchuifon Donald Raoul ◽  
Nche George Ndifor-Angwafor ◽  
Ngakou Sadeu Christian ◽  
Kamgaing Théophile ◽  
Ngomo Horace Manga ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Rice Husk ◽  
Order Kinetic ◽  
Adsorption Model ◽  
Batch Technique ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Adsorbed Quantity ◽  
Minimal Mass ◽  
Modified Adsorbents

<p>The present study is based on the adsorption of cadmium (II) ions on rice husk and egussi peeling, unmodified and modified with nitric acid in aqueous solution, using batch technique. It was carried out as a function of contact time, dosage, pH and initial concentration. The equilibrium time was achieved within 25 minutes for unmodified rice husk (Glu NT) and 20 minutes for unmodified egussi peeling (Cuc NT) with an adsorbed quantity of 13.18 mg/g. In the case of modified materials, we obtained 15 minutes for modified rice husk (Glu HNO3) and 10 minutes for modified egussi peeling (Cuc HNO3) with an adsorbed quantity of 18.77 mg/g. The maximum biosorption occurred at pH 5.5 for all biosorbents. The adsorbent mass for maximum adsorption was 0.4 g giving an adsorption capacity of 62.02 % for unmodified adsorbents. In the case of modified adsorbents, the minimal mass at which maximum adsorption occurred was 0.4 g giving an adsorption capacity of 98.33 % and 0.6 g giving an adsorption capacity of 98.33 % for modified rice husk and egussi peeling respectively. The adsorbent/adsorbate equilibrium was well described by the pseudo-second order kinetic model and by Langmuir’s and Freundlich adsorption model. This models showed that the adsorption of cadmium (II) is a chemisorption process.</p>

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