scholarly journals Dysprosium Removal from Water Using Active Carbons Obtained from Spent Coffee Ground

Author(s):  
Lorena Alcaraz ◽  
María Esther Escudero ◽  
Francisco J. Alguacil ◽  
Irene Llorente ◽  
Ana Urbieta ◽  
...  

This paper describes the physico-chemical study of the adsorption of dysprosium (Dy3+) in aqueous solution onto two types of activated carbons synthesized from spent coffee ground. KOH activated carbon is a microporous material with a specific BET surface area of 2330 m2·g-1 and pores with a diameter of 3.2 nm. Carbon activated with water vapor and N2 is a solid mesoporous, with pores of 5.7 nm in diameter and a specific surface of 982 m2·g-1. A significant dependence of the adsorption capacity on the solution pH was found, while it does not depend significantly neither on the dysprosium concentration nor on the temperature. A maximum adsorption capacity of 31.26 mg·g-1 and 33.52 mg·g-1 for the chemically and physically activated carbons, respectively, were found. In both cases, the results obtained from adsorption isotherms and kinetic study were better fit to a Langmuir model and a pseudo-second-order kinetics. In addition, thermodynamic results indicate that dysprosium adsorption onto both activated carbons is an exothermic, spontaneous and favorable process.

Nanomaterials ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1372 ◽  
Author(s):  
Lorena Alcaraz ◽  
María Esther Escudero ◽  
Francisco José Alguacil ◽  
Irene Llorente ◽  
Ana Urbieta ◽  
...  

This paper describes the physicochemical study of the adsorption of dysprosium (Dy3+) in aqueous solution onto two types of activated carbons synthesized from spent coffee ground. Potassium hydroxide (KOH)-activated carbon is a microporous material with a specific Brunauer–Emmett–Teller (BET) surface area of 2330 m2·g−1 and pores with a diameter of 3.2 nm. Carbon activated with water vapor and N2 is a solid mesoporous, with pores of 5.7 nm in diameter and a specific surface of 982 m2·g−1. A significant dependence of the adsorption capacity on the solution pH was found, but it does not significantly depend on the dysprosium concentration nor on the temperature. A maximum adsorption capacity of 31.26 mg·g−1 and 33.52 mg·g−1 for the chemically and physically activated carbons, respectively, were found. In both cases, the results obtained from adsorption isotherms and kinetic study were better a fit to the Langmuir model and pseudo-second-order kinetics. In addition, thermodynamic results indicate that dysprosium adsorption onto both activated carbons is an exothermic, spontaneous, and favorable process.


2015 ◽  
Vol 15 (3) ◽  
pp. 649-655 ◽  
Author(s):  
Husam Faiz Haddad ◽  
Azhagapillai Prabhu ◽  
Ahmed Al Shoaibi ◽  
Chandrasekar Srinivasakannan

The adsorption of benzene, toluene and xylene (BTX) was investigated covering different types of commercially available activated carbons with varied surface area and surface functional groups. The physico-chemical properties were characterized by Brunauer–Emmett–Teller (BET) surface area analysis, Fourier transform infrared (FTIR) spectroscopy and the Boehm titration method. Experiments to assess the adsorption isotherms and kinetics of adsorption were performed and the results are presented. An increase in the surface acid functional groups was found to decrease the adsorption capacity, with the highest adsorption capacity corresponding to carbon with lowest acid functionality.


2012 ◽  
Vol 610-613 ◽  
pp. 1701-1704
Author(s):  
Man Cheng Zhang ◽  
Wei Wang ◽  
Cong Jian Huang ◽  
Ai Min Li

The adsorption behaviors of chlortetracycline on two kinds of granular activated carbons with different BET surface area and average pore width have been studied. The results show that larger BET surface area is beneficial for the adsorption capacity, and wider pore structure can enhance the adsorption rate. Initial solution pH has great effect on the adsorption behavior, and the suitable pH for the effective adsorption is from 4 to 8.


2013 ◽  
Vol 295-298 ◽  
pp. 1321-1326 ◽  
Author(s):  
Kun Wu ◽  
Ting Liu ◽  
Jun Ming Peng

This study investigates the adsorption characteristics of As(V) onto the Fe-based backwashing sludge (FBBS), which was produced in the Fe(II) removal process. FBBS exhibits rough surfaces and shows high BET surface area of 148.41 m2/g. According to the results of EDS and XRD, the main constituents include sulfate inter-layered Fe hydroxide [Fe(SO4)OH], ferric oxhydroxide (γ-FeOOH), quartz (SiO2), and calcium carbonate (CaCO3). The adsorption kinetics data were well described by the Elovich model (r2 = 0.993), indicating the highly heterogeneous adsorption. The maximum adsorption capacity of As(V) increased from 40.04 to 88.76 mg/g as temperatures increased from 298 to 318 K, suggesting an endothermic process. The removal of As(V) was inhibited with elevated solution pH, especially from pH 7.0 to pH 10.0. Moreover, the removal of As(V) was enhanced with an increase in ion strength (0.01-1 M NaNO3), implying that the adsorption of As(V) was mainly through inner-sphere complexes mechanism.


J ◽  
2021 ◽  
Vol 4 (2) ◽  
pp. 193-205
Author(s):  
Opeyemi A. Oyewo ◽  
Sam Ramaila ◽  
Lydia Mavuru ◽  
Taile Leswifi ◽  
Maurice S. Onyango

The presence of toxic metals in surface and natural waters, even at trace levels, poses a great danger to humans and the ecosystem. Although the combination of adsorption and coagulation techniques has the potential to eradicate this problem, the use of inappropriate media remains a major drawback. This study reports on the application of NaNO2/NaHCO3 modified sawdust-based cellulose nanocrystals (MCNC) as both coagulant and adsorbent for the removal of Cu, Fe and Pb from aqueous solution. The surface modified coagulants, prepared by electrostatic interactions, were characterized using Fourier transform infrared, X-ray diffraction (XRD), and scanning electron microscopy/energy-dispersive spectrometry (SEM/EDS). The amount of coagulated/adsorbed trace metals was then analysed using inductively coupled plasma atomic emission spectroscopy (ICP-AES). SEM analysis revealed the patchy and distributed floccules on Fe-flocs, which was an indication of multiple mechanisms responsible for Fe removal onto MCNC. A shift in the peak position attributed to C2H192N64O16 from 2θ = 30 to 24.5° occurred in the XRD pattern of both Pb- and Cu-flocs. Different process variables, including initial metal ions concentration (10–200 mg/L), solution pH (2–10), and temperature (25–45 °C) were studied in order to investigate how they affect the reaction process. Both Cu and Pb adsorption followed the Langmuir isotherm with a maximum adsorption capacity of 111.1 and 2.82 mg/g, respectively, whereas the adsorption of Fe was suggestive of a multilayer adsorption process; however, Fe Langmuir maximum adsorption capacity was found to be 81.96 mg/g. The sequence of trace metals removal followed the order: Cu > Fe > Pb. The utilization of this product in different water matrices is an effective way to establish their robustness.


Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 63
Author(s):  
Maria Harja ◽  
Gabriela Buema ◽  
Nicoleta Lupu ◽  
Horia Chiriac ◽  
Dumitru Daniel Herea ◽  
...  

Fly ash/magnetite material was used for the adsorption of copper ions from synthetic wastewater. The obtained material was characterized by scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX), X-ray diffractometer (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET) surface area, and vibrating sample magnetometer (VSM). Batch adsorption experiments were employed in order to investigate the effects of adsorbent dose, initial Cu (II) concentration and contact time over adsorption efficiency. The experimental isotherms were modeled using Langmuir (four types of its linearization), Freundlich, Temkin, and Harkins–Jura isotherm models. The fits of the results are estimated according to the Langmuir isotherm, with a maximum adsorption capacity of 17.39 mg/g. The pseudo-second-order model was able to describe kinetic results. The data obtained throughout the study prove that this novel material represents a potential low-cost adsorbent for copper adsorption with improved adsorption capacity and magnetic separation capability compared with raw fly ash.


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3718
Author(s):  
Mohammad Azam ◽  
Saikh Mohammad Wabaidur ◽  
Mohammad Rizwan Khan ◽  
Saud I. Al-Resayes ◽  
Mohammad Shahidul Islam

The aim of the research was to prepare low-cost adsorbents, including raw date pits and chemically treated date pits, and to apply these materials to investigate the adsorption behavior of Cr(III) and Cd(II) ions from wastewater. The prepared materials were characterized using SEM, FT-IR and BET surface analysis techniques for investigating the surface morphology, particle size, pore size and surface functionalities of the materials. A series of adsorption processes was conducted in a batch system and optimized by investigating various parameters such as solution pH, contact time, initial metal concentrations and adsorbent dosage. The optimum pH for achieving maximum adsorption capacity was found to be approximately 7.8. The determination of metal ions was conducted using atomic adsorption spectrometry. The experimental results were fitted using isotherm Langmuir and Freundlich equations, and maximum monolayer adsorption capacities for Cr(III) and Cd(II) at 323 K were 1428.5 and 1302.0 mg/g (treated majdool date pits adsorbent) and 1228.5 and 1182.0 mg/g (treated sagai date pits adsorbent), respectively. It was found that the adsorption capacity of H2O2-treated date pits was higher than that of untreated DP. Recovery studies showed maximal metal elution with 0.1 M HCl for all the adsorbents. An 83.3–88.2% and 81.8–86.8% drop in Cr(III) and Cd(II) adsorption, respectively, were found after the five regeneration cycles. The results showed that the Langmuir model gave slightly better results than the Freundlich model for the untreated and treated date pits. Hence, the results demonstrated that the prepared materials could be a low-cost and eco-friendly choice for the remediation of Cr(III) and Cd(II) contaminants from an aqueous solution.


2020 ◽  
Vol 83 (1) ◽  
pp. 27-36
Author(s):  
Mardawani Mohamad ◽  
Rizki Wannahari ◽  
Rosmawani Mohammad ◽  
Noor Fazliani Shoparwe ◽  
Kwan Wei Lun ◽  
...  

Used coffee grounds usually end up as landfill. However, the unique structural properties of its porous surface make coffee grounds can be transformed into biochar and performed as an alternative low cost adsorbent. Malachite green (MG) is a readily water soluble dye which is used extensively in textile and aquaculture industries. The mordant complex structures of MG generate destructive effects to animals and environment. In this study, adsorption of malachite green using spent coffee ground biochar as adsorbent was investigated. The experiments were designed in two methods: classical and optimisation by response surface methodology. Three parameters were studied, which are adsorbent dosage, contact time and pH while the responses in this study are malachite green removal (%) and adsorption capacity (mg/g). Optimisation studies were performed using response surface methodology. Quadratic model was chosen for both response and studied using central composite design. The correlation coefficient, R2 for the quadratic model of malachite green removal (%) and adsorption capacity (mg/g) were 0.95 and 0.99, respectively. The optimum malachite green removal (%) predicted was found at 99.27%, by using 0.12 g of adsorbent dosage, 43.05 minutes of contact time and pH of 9.45 at desirability of 1.0. The optimum adsorption capacity (mg/g) predicted was found at 118.01 mg/g, by using 0.02 g of adsorbent dosage, 60 minutes of contact time and pH of 10.24 at desirability of 0.98. So, it was concluded that the spent coffee ground biochar can be used as an effective adsorbent for malachite green removal from aqueous solution.


2020 ◽  
Vol 82 (5) ◽  
pp. 984-997
Author(s):  
Tatyana Kouznetsova ◽  
Andrei Ivanets ◽  
Vladimir Prozorovich ◽  
Ahmad Hosseini-Bandegharaei ◽  
Hai Nguyen Tran ◽  
...  

Abstract The research aimed to develop a novel mesoporous aluminosilicate/zeolite composite by the template co-precipitation method. The effect of aluminosilicate (AlSi) and zeolite (NaY) on the basic properties and adsorption capacity of the resultant composite was conducted at different mass ratios of AlSi/NaY (i.e., 5/90, 10/80, 15/85, 20/80, and 50/50). The adsorption characteristics of such composite and its feedstock materials (i.e., aluminosilicates and zeolite) towards radioactive Sr2+ ions and toxic metals (Cu2+ and Pb2+ ions) in aqueous solutions were investigated. Results indicated that BET surface area (SBET), total pore volume (VTotal), and mesopore volume (VMeso) of prepared materials followed the decreasing order: aluminosilicate (890 m2/g, 0.680 cm3/g, and 0.644 cm3/g) > zeolite (623 m2/g, 0.352 cm3/g, and 0.111 cm3/g) > AlSi/NaY (20/80) composite (370 m2/g, 0.254 cm3/g, and 0.154 cm3/g, respectively). The Langmuir maximum adsorption capacity (Qm) of metal ions (Sr2+, Cu2+, and Pb2+) in single-component solution was 260 mg/g, 220 mg/g, and 161 mg/g (for zeolite), 153 mg/g, 37.9 mg/g, and 66.5 mg/g (for aluminosilicate), and 186 mg/g, 140 mg/g, and 77.8 mg/g for (AlSi/NaY (20/80) composite), respectively. Ion exchange was regarded as a domain adsorption mechanism of metal ions in solution by zeolite; meanwhile, inner-surface complexation was domain one for aluminosilicate. Ion exchange and inner-surface complexation might be mainly responsible for adsorbing metal ions onto the AlSi/NaY composite. Pore-filling mechanism was a less important contributor during the adsorption process. The results of competitive adsorption under binary-components (Cu2+ and Sr2+) and ternary-components (Cu2+, Pb2+, and Sr2) demonstrated that the removal efficacy of target metals by the aluminosilicate, zeolite, and their composite remarkably decreased. The synthesized AlSi/NaY composite might serve as a promising adsorbent for real water treatment.


Author(s):  
Nguyen Thi Minh Tam ◽  
Yunguo Liu ◽  
Hassan Bashir ◽  
Zhihong Yin ◽  
Yuan He ◽  
...  

Porous graphitic biochar was synthesized by one-step treatment biomass using potassium ferrate (K2FeO4) as activator for both carbonization and graphitization processes. The modified biochar (Fe@BC) was applied for the removal of diclofenac sodium (DCF) in an aqueous solution. The as-prepared material possesses a well-developed micro/mesoporous and graphitic structure, which can strengthen its adsorption capacity towards DCF. The experimental results indicated that the maximum adsorption capacity (qmax) of Fe@BC for DCF obtained from Langmuir isotherm simulation was 123.45 mg·L−1 and it was a remarkable value of DCF adsorption in comparison with that of other biomass-based adsorbents previously reported. Thermodynamic quality and effect of ionic strength studies demonstrated that the adsorption was a endothermic process, and higher environmental temperatures may be more favorable for the uptake of DCF onto Fe@BC surface; however, the presence of NaCl in the solution slightly obstructed DCF adsorption. Adsorption capacity was found to be decreased with the increase of solution pH. Additionally, the possible mechanism of the DCF adsorption process on Fe@BC may involve chemical adsorption with the presence of H-bonding and π–π interaction. With high adsorption capacity and reusability, Fe@BC was found to be a promising absorbent for DCF removal from water as well as for water purification applications.


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