scholarly journals Surface Interactions during the Removal of Emerging Contaminants by Hydrochar-Based Adsorbents

Molecules ◽  
2020 ◽  
Vol 25 (9) ◽  
pp. 2264 ◽  
Author(s):  
Silvia Román ◽  
Joâo Manuel Valente Nabais ◽  
Beatriz Ledesma ◽  
Carlos Laginhas ◽  
Maria-Magdalena Titirici
Keyword(s):  
Nicotinic Acid ◽  
Adsorption Capacity ◽  
Emerging Contaminants ◽  
Activated Carbons ◽  
Surface Acidity ◽  
Maximum Adsorption Capacity ◽  
Adsorption Mechanisms ◽  
Olive Stone ◽  
Steric Factors ◽  
Negative Ionization

The aim of this work was to test activated carbons derived from hydrochars produced from sunflower stem, olive stone and walnut shells, as adsorbents for emerging contaminants in aqueous solution, namely fluoxetine and nicotinic acid. The adsorption capacity was determined by the chemical nature of the adsorbents, namely the presence of specific functional groups and their positive or negative ionization in aqueous solutions and also by steric factors. The activated carbons produced by air showed a higher adsorption capacity of fluoxetine, whilst the samples produced by carbon dioxide activation were more useful to remove nicotinic acid. In general, surface acidity was advantageous for fluoxetine adsorption and detrimental for nicotinic acid removal. The adsorption mechanisms involved in each case were discussed and related to the adsorbents characteristics. The maximum adsorption capacity, Q0, given by the Langmuir model was 44.1 and 91.9 mg g−1 for fluoxetine and nicotinic acid adsorption, respectively.

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

2019 ◽  
Author(s):  
Lorena Alcaraz ◽  
María Esther Escudero ◽  
Francisco J. Alguacil ◽  
Irene Llorente ◽  
Ana Urbieta ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Activated Carbons ◽  
Chemical Study ◽  
Bet Surface Area ◽  
Maximum Adsorption Capacity ◽  
Solution Ph ◽  
Microporous Material ◽  
Physico Chemical ◽  
Spent Coffee Ground ◽  
Coffee Ground

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.

scholarly journals The Triple Mechanisms of Atenolol Adsorption on Ca-Montmorillonite: Implication in Pharmaceutical Wastewater Treatment

Materials ◽  
2019 ◽  
Vol 12 (18) ◽  
pp. 2858 ◽  
Author(s):  
Po-Hsiang Chang ◽  
Wei-Teh Jiang ◽  
Binoy Sarkar ◽  
Wendong Wang ◽  
Zhaohui Li
Keyword(s):  
Adsorption Capacity ◽  
Clay Mineral ◽  
Basal Spacing ◽  
Maximum Adsorption Capacity ◽  
Pharmaceutical Wastewater ◽  
Absorption Bands ◽  
Adsorption Mechanisms ◽  
Adsorption Sites ◽  
Dioctahedral Smectite ◽  
Β Receptor

The adsorption of atenolol (AT) from aqueous solutions by Ca-montmorillonite (SAz-2) was investigated in batch studies under different physicochemical conditions. The AT existed in neutral un-dissociated form at pH 10, and was adsorbed on dioctahedral smectite (SAz-2) obeying the Langmuir isotherm with a maximum adsorption capacity of 330 mmol/kg. The kinetic adsorption suggested that both strong and weak adsorption sites existed on SAz-2 and participated in the adsorption mechanisms. The amount of exchangeable cations desorbed from SAz-2 during AT adsorption was linearly correlated with the amounts of adsorbed AT having slopes of 0.43, which implied that a cation exchange based adsorption mechanism was also in place. A comprehensive basal spacing change of SAz-2 was observed after AT adsorption on the clay mineral when tested with or without AT recrystallization. The intercalation of AT into the SAz-2 interlayers did not result in swelling due to the low adsorption capacity of the drug. Prominent interactions between the pharmaceutical molecule and SAz-2 were evidenced by apparent shifts of the infrared absorption bands after adsorption. The interlayer configurations and hydrogen bonding of AT on SAz-2 were also supported by infrared, X-ray diffraction and thermogravimetric analyses. This study suggested that SAz-2 is an excellent material to remove not only AT from pharmaceutical wastewater, but can potentially remove many other β-receptor blocker drugs. The results helped us to understand the possible interlayer configurations and adsorption mechanisms of the drugs on natural clay mineral based adsorbents.

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

Nanomaterials ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1372 ◽  
Author(s):  
Lorena Alcaraz ◽  
María Esther Escudero ◽  
Francisco José Alguacil ◽  
Irene Llorente ◽  
Ana Urbieta ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Potassium Hydroxide ◽  
Activated Carbons ◽  
Bet Surface Area ◽  
Maximum Adsorption Capacity ◽  
Solution Ph ◽  
Microporous Material ◽  
Spent Coffee Ground ◽  
Coffee Ground ◽  
Pseudo Second Order

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.

scholarly journals Preparation of GO/MIL-101(Fe,Cu) composite and its adsorption mechanisms for phosphate in aqueous solution

2021 ◽  
Author(s):  
You Wu ◽  
Zuannian Liu ◽  
Bakhtari Mohammad Fahim ◽  
Junnan Luo
Keyword(s):  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Adsorption Mechanism ◽  
Nitrogen Adsorption ◽  
Adsorption Properties ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Adsorption Mechanisms ◽  
Adsorption Desorption

Abstract In this study, MIL-101(Fe), MIL-101(Fe,Cu), and Graphene Oxide (GO) /MIL-101(Fe,Cu) were synthesized to compose a novel sorbent. The adsorption properties of these three MOFs-based composites were compared toward the removal of phosphate. Furthermore, the influencing factors including reaction time, pH, temperature and initial concentration on the adsorption capacity of phosphate on these materials as well as the reusability of the material were discussed. The structure of fabricated materials and the removal mechanism of phosphate on the composite material were analyzed by Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption-desorption analysis and zeta potential. The results show that the maximum adsorption capacity of phosphate by the composite GO/MIL-101(Fe,Cu)-2% was 204.60 mg·g− 1, which is higher than that of MIL-101(Fe,Cu) and MIL-101(Fe). likewise the specific surface area of GO/MIL-101(Fe,Cu)-2% is 778.11 m2/g is higher than that of MIL-101(Fe,Cu) and MIL-101(Fe),which are 747.75 and 510.66m2/g respectively. The adsorption mechanism of phosphate is electrostatic attraction, form coordination bonds and hydrogen bonds. The fabricated material is a promising adsorbent for the removal of phosphate with good reusability.

scholarly journals The interaction of metallic ions onto activated carbon surface using computational chemistry software

2020 ◽  
Vol 38 (5-6) ◽  
pp. 191-204
Author(s):  
AL Paredes-Doig ◽  
A Pinedo-Flores ◽  
J Aylas-Orejón ◽  
D Obregón-Valencia ◽  
MR Sun Kou
Keyword(s):  
Activated Carbon ◽  
Metal Ions ◽  
Electron Density ◽  
Activated Carbons ◽  
Surface Acidity ◽  
Chemical Activation ◽  
Carbon Surface ◽  
Maximum Adsorption Capacity ◽  
Metallic Ions ◽  
Oxidized Activated Carbon

Activated carbon was prepared from the seeds of aguaje palm ( Mauritia flexuosa L.f.) by a chemical activation with phosphoric acid. This activated carbon was used for adsorbing metal ions: Pb(II), Cd(II), and Cr(III). To understand the mechanism of adsorption of these heavy metals (Cr, Cd, and Pb), the activated carbon surface was oxidized with nitric acid (1 M) increasing the oxygenated surface groups showing an increasing in their adsorption capacities of these metals. The oxidized activated carbon slightly increased the maximum adsorption capacity to 5–7%. The order of adsorption for unoxidized and oxidized activated carbons was Pb> Cd> Cr. This experimental information was corroborated by molecular modeling program Hyperchem 8 based adsorption mainly on two factors: the electron density and orbitals—highest occupied molecular orbital and lowest unoccupied molecular orbital.Activated carbons were characterized by adsorption/desorption of N2, obtaining an increase of microporous surface area for oxidized activated carbon. An increase of surface acidity and a reduction of isoelectric points were observed in oxidized activated carbon. According to these results, the adsorption of metal ions is favored in contact with an oxidized activated carbon, which has more amount of phenolic and carboxylic functional groups. Similarly, decreasing the isoelectric point indicates that the surface has a higher negative charge. The surface information was corroborated by Hyperchem, which indicates that the surface of the oxidized activated carbon has a higher electron density, indicating a larger amount of electrons on its surface, which means the surface of oxidized activated carbon charges negatively and thereby attracts metal ions.

scholarly journals Fe(III) Complexed Polydopamine Modified Mg/Al Layered Double Hydroxide Enhances The Removal of Cr(VI) From Aqueous Solutions

2021 ◽  
Author(s):  
Changcheng Chen ◽  
Mina Luo ◽  
Fu Chen ◽  
Chao Huang ◽  
Chunmei Zhu ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Adsorption Mechanisms ◽  
Removal Capacity ◽  
Double Hydroxide ◽  
Double Hydroxides ◽  
Influence Of Ph

Abstract Herein, we report the preparation of Fe(III) complexed polydopamine modified Mg/Al layered double hydroxides composite material (LDHs@PDA-Fe(III)) and its application to the removal of Cr(VI) in aqueous solution. LDHs@PDA-Fe(III) was characterized and analyzed by field-emission scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), Fourier transformed infrared (FTIR), X-ray diffraction (XRD), X-ray photoelectron (XPS). The adsorption performance was studied through a series of adsorption experiments. Under the influence of pH, time, temperature, concentration, the maximum adsorption capacity obtained in the experiment is 683.4 mg/g. In addition, after 5 adsorption cycles, LDHs@PDA-Fe(III) still shows excellent adsorption capacity and stability. Combining adsorption experiments and characterization analysis, it is inferred that the adsorption of Cr(VI) by LDHs@PDA-Fe(III) is the result of the synergistic effect of multiple adsorption mechanisms. Therefore, the efficient removal capacity and excellent stability make LDHs@PDA-Fe(III) an ideal adsorbent for removing Cr(VI) from aqueous solutions.

scholarly journals Thermal Activation of Digested Sewage Sludges for Carbon Dioxide Removal from Biogas

Fuels ◽  
2020 ◽  
Vol 1 (1) ◽  
pp. 30-46
Author(s):  
Mirko Tinnirello ◽  
Davide Papurello ◽  
Massimo Santarelli ◽  
Sonia Fiorilli
Keyword(s):  
Adsorption Capacity ◽  
Dwell Time ◽  
Activated Carbons ◽  
Co2 Concentration ◽  
Physical Activation ◽  
Maximum Adsorption Capacity ◽  
Activation Process ◽  
Co2 Removal ◽  
Sewage Sludges ◽  
Activating Agent

Anaerobically digested sewage sludges were used as feedstock in the production of activated carbons through physical activation. These char samples were experimentally tested as adsorbents for the removal of CO2 from a simulated biogas mixture. The CO2 concentration level allowed in biomethane was fixed from the European Standards EN 16723-1 and EN 16723-2. The char yield and the subsequent adsorption capacity values were studied, considering the operating parameters of the process. A physical activation process was considered with the following parameters: the temperature, the dwell time, the activating agent, the heating rate, the flow rate, and the method. Among the adsorption tests, the activating temperature and the agent employed affected the CO2 removal. The maximum adsorption capacity was achieved with nitrogen as an activating agent at 600 °C, with 2 h of dwell time (102.5 mg/g).

scholarly journals Preparation of Activated Carbons from Spent Coffee Grounds and Coffee Parchment and Assessment of Their Adsorbent Efficiency

Processes ◽  
2021 ◽  
Vol 9 (8) ◽  
pp. 1396
Author(s):  
Gustavo A. Figueroa Campos ◽  
Jeffrey Paulo H. Perez ◽  
Inga Block ◽  
Sorel Tchewonpi Sagu ◽  
Pedro Saravia Celis ◽  
...  
Keyword(s):  
Lactic Acid ◽  
Activated Carbon ◽  
Adsorption Capacity ◽  
Activated Carbons ◽  
Low Cost ◽  
Maximum Adsorption Capacity ◽  
Spent Coffee Grounds ◽  
Hydrophobic Compounds ◽  
Coffee Grounds ◽  
By Products

The valorization of coffee wastes through modification to activated carbon has been considered as a low-cost adsorbent with prospective to compete with commercial carbons. So far, very few studies have referred to the valorization of coffee parchment into activated carbon. Moreover, low-cost and efficient activation methods need to be more investigated. The aim of this work was to prepare activated carbon from spent coffee grounds and parchment, and to assess their adsorption performance. The co-calcination processing with calcium carbonate was used to prepare the activated carbons, and their adsorption capacity for organic acids, phenolic compounds and proteins was evaluated. Both spent coffee grounds and parchment showed yields after the calcination and washing treatments of around 9.0%. The adsorption of lactic acid was found to be optimal at pH 2. The maximum adsorption capacity of lactic acid with standard commercial granular activated carbon was 73.78 mg/g, while the values of 32.33 and 14.73 mg/g were registered for the parchment and spent coffee grounds activated carbons, respectively. The Langmuir isotherm showed that lactic acid was adsorbed as a monolayer and distributed homogeneously on the surface. Around 50% of total phenols and protein content from coffee wastewater were adsorbed after treatment with the prepared activated carbons, while 44, 43, and up to 84% of hydrophobic compounds were removed using parchment, spent coffee grounds and commercial activated carbon, respectively; the adsorption efficiencies of hydrophilic compounds ranged between 13 and 48%. Finally, these results illustrate the potential valorization of coffee by-products parchment and spent coffee grounds into activated carbon and their use as low-cost adsorbent for the removal of organic compounds from aqueous solutions.

scholarly journals Cu(II) and Cd(II) Removal from Aqueous Solution with LDH@GO-NH2 and LDH@GO-SH: Kinetics and Probable Mechanism

2021 ◽  
Author(s):  
Wei Liao ◽  
Di Bao ◽  
Huiqiang Li ◽  
Ping Yang
Keyword(s):  
Adsorption Capacity ◽  
Thiol Group ◽  
Maximum Adsorption Capacity ◽  
Isomorphic Substitution ◽  
Temperature Dependent ◽  
Adsorption Mechanisms ◽  
Adsorption Processes ◽  
Endothermic Process ◽  
Pseudo Second Order ◽  
Near Future

Abstract Two novel adsorbents of thiol- and amino-functionalized GO grafted onto LDH (LDH@GO-NH2 and LDH@GO-SH) were synthesized and contrasted for adsorption properties for Cu(II) and Cd(II). Characterization experiments illustrated that thiol group (-SH) and amino group (-NH2) were existed onto LDH@GO-NH2 and LDH@GO-SH. Adsorption isotherm results showed that the adsorption processes were satisfactorily fitted by both Langmuir and Freundlich models. The maximum adsorption capacity of Cd(II) on LDH@GO-SH at 308 K was 102.77 mg/g, which was about triple that of LDH@GO-NH2. The enhancement in adsorption capacity was due to the cooperative effect of LDH and GO-SH. The kinetic experimental data for LDH@GO-NH2 and LDH@GO-SH were found to be in good agreement with pseudo-second-order model. The thermodynamic parameters calculated from the temperature dependent adsorption isotherms indicated that the adsorption was a spontaneous and endothermic process. The possible adsorption mechanisms comprising formation of precipitation, isomorphic substitution of Mg(II), and formation of complexation with amino-groups and thiol-groups were proposed. Desorption experiments put into evidence that the LDH@GO-NH2 and LDH@GO-SH may be promising suitable candidates for the remediation of metal ions from aqueous solutions in real work in the near future.

scholarly journals Adsorption of Cd, Cu, Ni and Zn in tropical soils under competitive and non-competitive systems

2010 ◽  
Vol 67 (3) ◽  
pp. 301-307 ◽  
Author(s):  
Cindy Silva Moreira ◽  
Luís Reynaldo Ferracciú Alleoni
Keyword(s):  
Adsorption Capacity ◽  
Tropical Soils ◽  
Langmuir Model ◽  
Tropical Region ◽  
Maximum Adsorption Capacity ◽  
Competitive System ◽  
Adsorption Mechanisms ◽  
Competitive Systems ◽  
Metal Affinity ◽  
Surface Samples

The adsorption of heavy metals in soils affects their behavior in the environment and their bioavailability to plants. The knowledge of the adsorption mechanisms in competitive systems allows a more realistic evaluation of the metals' behavior in the soil than the single metal adsorption. The objectives of this study were (i) to evaluate Cd, Cu, Ni, and Zn adsorption in 14 surface samples (0-0.2 m) of representative soils of the Brazilian humid-tropical region, in competitive and non-competitive systems, and (ii) to establish metal affinity sequences for each soil, based in the maximum adsorption capacity (MAC) estimated by the Langmuir model. The Rhodic Eutrudox, the Kandiudalf Eutrudox, the Arenic Hapludalf, the Arenic Hapludult and the Typic Argiudoll had the highest metals' adsorption capacity, whereas the Typic Quartzipsamment and the sandy-textured Arenic Hapludult had the lowest values. In general, the MAC values for metals were lower in the competitive than in the non-competitive system. In the non-competitive system, the most common affinity sequence was Cu > Zn > Ni > Cd, whereas the most common sequence was Cu > Cd > Zn > Ni in the competitive system. In general, the Langmuir model fitted well the adsorption data of metals on the studied soils.

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