scholarly journals Cd(II) removal from aqueous solutions by pomelo peel derived biochar in a permeable reactive barrier: Modelling, optimization and mechanism

2021 ◽  
Author(s):  
Gang Xiang ◽  
Shengxing Long ◽  
Xianliang Wu ◽  
Huijuan Liu
Keyword(s):  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Large Scale ◽  
Carbon Fixation ◽  
Absolute Error ◽  
Waste Recycling ◽  
Permeable Reactive Barrier ◽  
Experimental Conditions ◽  
Reactive Barrier ◽  
Pomelo Peel

Abstract Biochar can have multiple benefits, such as solid waste recycling, water pollution treatment, carbon fixation and sustainability. The present study aimed to investigate Cd(II) removal from aqueous solutions using pomelo peel derived biochar combined with a permeable reactive barrier (PRB). The results show that there were slight changes in the structure of the pomelo peel derived biochar before and after activation, while the variation was not significant. The specific surface areas of the not activated and activated pomelo peel derived biochars were 3.207 m2/g and 6.855 m2/g, respectively. The pore diameter of the former was 4.165 nm and that of the latter was 4.425 nm, indicating that the two materials are mainly mesoporous. BP-GA was more suitable than RSM for optimizing the removal conditions of Cd(II) using the prepared materials combined with PRB. The maximum removal efficiency of Cd(II) was 90.31% at biochar dosage = 4.84, reaction time = 53.75 min, initial Cd(II) concentration = 19.36 mg/L and initial pH = 6.07. The verification experiment was 88.74% under these experimental conditions, and the absolute error was 1.57%. The saturated adsorption capacity of quartz sand for Cd(II) is approximately 0.08 mg/g when reaching equilibrium. The saturated adsorption capacity of biochar for Cd(II) is approximately 29.76 mg/g. Pseudo second order kinetics and Langmuir isotherm adsorption were more suitable for describing the Cd(II) adsorbed from an aqueous solution by activated pomelo peel derived biochar. The adsorption process of Cd(II) by the prepared biochar was spontaneous, endothermic and entropy driven. Our results suggest that the modified biochar can be regenerated within the fourth cycle and that it has application prospects as a useful adsorbent for water treatment in PRB systems. This finding provides a reference for relieving Cd pollution and for its large scale removal from wastewater when combined with a PRB system.

Commercial Activated Carbon Modified with Sulfuric Acid: A Potential Permeable Reactive Barrier Material for In Situ Remediation of Cr(VI) from Groundwater

2011 ◽  
Vol 343-344 ◽  
pp. 172-176
Author(s):  
Jun Ping Liu ◽  
Huan Zhen Zhang ◽  
Xiao Meng Liu
Keyword(s):  
Activated Carbon ◽  
Sulfuric Acid ◽  
Adsorption Capacity ◽  
Permeable Reactive Barrier ◽  
Contaminated Groundwater ◽  
Batch Studies ◽  
Reactive Barrier ◽  
Chemically Modified ◽  
Synthetic Groundwater

In this study, removal of Cr(Ⅵ) from synthetic groundwater by adsorption onto commercial activated carbon (CAC) made up of coconut shell is investigated in batch studies. Surface modification of CAC with sulfuric acid is also conducted to evaluate its removal performance. It is evident that CAC chemically modified with sulfuric acid (sulfuric-treated CAC) demonstrates higher Cr(Ⅵ) removal efficiency than non-treated CAC in dealing with contaminated groundwater with the pH is about 7.0, suggesting that sulfuric-treated CAC is suitable for the in-situ remediation of Cr(Ⅵ) contaminated groundwater. Adsorption of Cr(Ⅵ) is strongly affected by pH, the granular sulfuric-treated CAC exhibits the highest Cr(Ⅵ) adsorption capacity at pH 1.5 and the maximum Cr(Ⅵ) adsorption capacity of which estimated with the Langmuir model was 8.24mg/g.

scholarly journals Examination of the Effectiveness of Physical and Chemical Activation of Natural Bentonite for the Removal of Heavy Metal Ions from Aqueous Solutions

2002 ◽  
Vol 20 (2) ◽  
pp. 151-167 ◽  
Author(s):  
Fawzi Banat ◽  
Sameer Al-Asheh ◽  
Leena Abu-Aitah
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Adsorption Capacity ◽  
Chemical Activation ◽  
Sodium Dodecyl ◽  
Batch Adsorption ◽  
Initial Material ◽  
Solution Ph ◽  
Experimental Conditions ◽  
Activated Bentonite

The ability of physically and chemically activated bentonite to adsorb copper and nickel ions from aqueous solutions was examined under various experimental conditions. Physically activated bentonite was obtained by thermal treatment of the initial material in an oven at 700°C (T-bentonite), while chemically activated bentonite was obtained in two ways, either by treatment of the initial material with sodium dodecyl sulphate (SDS) as an anionic surfactant to give SDS-bentonite or with aluminium hydroxypolycation as a pillaring agent to give Al-bentonite. Batch adsorption tests were undertaken to study the removal of Cu2+ and Ni2+ ions from aqueous solutions using the above-mentioned types of activated bentonite. The adsorption capacity of the bentonites towards both Cu2+ and Ni2+ ions followed the order: Al-bentonite > SDS-bentonite > T-bentonite > natural bentonite. The initial metal concentration, solution pH, temperature and salinity of the solution affected the adsorption capacity towards both metal ions. The uptake of Cu2+ ions increased with an increase in temperature (25–45°C) as well as with an increase in the initial pH of the solution (3–5). The uptake of Cu2+ and Ni2+ ions decreased significantly with an increase in the NaCl and KCl concentrations present in the aqueous solution. Sulphuric acid of 0.1 M concentration was found to be an effective desorbent for bentonite laden with heavy metals.

scholarly journals Enhanced adsorption removal of anionic dyes via a facile preparation of amino-functionalized magnetic silica

2017 ◽  
Vol 75 (6) ◽  
pp. 1399-1409 ◽  
Author(s):  
Xiao-Shui Li ◽  
Yu-Han Fan ◽  
Shou-Wen Zhang ◽  
Shi-Hua Qi
Keyword(s):  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Maximum Adsorption Capacity ◽  
Reactive Black 5 ◽  
Order Kinetic ◽  
Step Method ◽  
Anionic Dyes ◽  
Solution Ph ◽  
Experimental Conditions ◽  
Magnetic Silica

A novel amino-functionalized magnetic silica (Fe3O4@SiO2-NH2) was easily prepared via a one-step method integrating the immobilization of 3-aminopropyltriethoxysilane with a sol-gel process of tetraethyl orthosilicate into a single process. This showed significant improvement in the adsorption capacity of anionic dyes. The product (Fe3O4@SiO2-NH2) was characterized with scanning electron microscopy, Fourier transform infrared spectroscopy, energy dispersive X-ray spectrometry, zeta potential and vibrating sample magnetometry. The adsorption performance of Fe3O4@SiO2-NH2 was then tested by removing acid orange 10 (AO10) and reactive black 5 (RB5) from the aqueous solutions under various experimental conditions including initial solution pH, initial dye concentrations, reaction time and temperature. The results indicated that the maximum adsorption capacity of AO10 and RB5 on Fe3O4@SiO2-NH2 was 621.9 and 919.1 mg g−1 at pH 2, respectively. The sorption isotherms fit the Langmuir model nicely. Similarly, the sorption kinetic data were better fitted into the pseudo-second order kinetic model than the pseudo-first order model. In addition, the thermodynamic data demonstrated that the adsorption process was endothermic, spontaneous and physical. Furthermore, Fe3O4@SiO2-NH2 could be easily separated from aqueous solutions by an external magnetic field, and the preparation was reproducible.

scholarly journals Adsorption of Pb2+ ions from aqueous solutions by gelatin/activated carbon composite bead form

2017 ◽  
Vol 36 (1-2) ◽  
pp. 355-371 ◽  
Author(s):  
Fareeda Hayeeye ◽  
Qiming J Yu ◽  
Memoon Sattar ◽  
Watchanida Chinpa ◽  
Orawan Sirichote
Keyword(s):  
Activated Carbon ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Ph Value ◽  
Carbon Composite ◽  
Batch Adsorption ◽  
Maximum Adsorption Capacity ◽  
Solution Ph ◽  
Experimental Conditions ◽  
Composite Bead

Gelatin and activated carbon materials have been combined together to obtain a gelatin/activated carbon composite bead form which is ecofriendly, nontoxic, biocompatible, and inexpensive material. In this paper, gelatin/activated carbon adsorption for Pb2+ ions from aqueous solutions was studied experimentally under various conditions. The experimental conditions such as contact time, solution pH, and gelatin/activated carbon dosage were examined and evaluated by using batch adsorption experiments. The maximum adsorption capacity of gelatin/activated carbon for Pb2+ ions was obtained to be 370.37 mg g−1. This maximum capacity was comparable with that of commercial ion exchange resins and it was much higher than those of natural zeolites. The uptake process for Pb2+ ions was found to be relatively fast with 92.15% of the adsorption completed in about 5 min in batch conditions. The adsorption capacity was also strongly solution pH dependent. Adsorption was observed at pH value as low as 2.0 and maximum adsorption was achieved at a pH of approximately 5. The results indicated that the gelatin/activated carbon was effective to be used as an adsorbent for Pb2+ ions removal in wastewater treatment.

Benchmark of Simplified Time-Dependent Density Functional Theory for UV-Vis Spectral Properties of Porphyrinoids

2019 ◽  
Author(s):  
Kamal Batra ◽  
Stefan Zahn ◽  
Thomas Heine
Keyword(s):  
Density Functional Theory ◽  
Density Functional ◽  
Large Scale ◽  
Absolute Error ◽  
Time Dependent ◽  
Basis Set ◽  
Basis Sets ◽  
Functional Theory ◽  
Framework Materials ◽  
Dependent Density

<p>We thoroughly benchmark time-dependent density- functional theory for the predictive calculation of UV/Vis spectra of porphyrin derivatives. With the aim to provide an approach that is computationally feasible for large-scale applications such as biological systems or molecular framework materials, albeit performing with high accuracy for the Q-bands, we compare the results given by various computational protocols, including basis sets, density-functionals (including gradient corrected local functionals, hybrids, double hybrids and range-separated functionals), and various variants of time-dependent density-functional theory, including the simplified Tamm-Dancoff approximation. An excellent choice for these calculations is the range-separated functional CAM-B3LYP in combination with the simplified Tamm-Dancoff approximation and a basis set of double-ζ quality def2-SVP (mean absolute error [MAE] of ~0.05 eV). This is not surpassed by more expensive approaches, not even by double hybrid functionals, and solely systematic excitation energy scaling slightly improves the results (MAE ~0.04 eV). </p>

Sorption of Bisphenol A in Aqueous Solutions on Irradiated and as-Grown Multiwalled Carbon Nanotubes

2018 ◽  
Vol 69 (5) ◽  
pp. 1233-1239
Author(s):  
Raluca Madalina Senin ◽  
Ion Ion ◽  
Ovidiu Oprea ◽  
Rusandica Stoica ◽  
Rodica Ganea ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Bisphenol A ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Multiwalled Carbon Nanotubes ◽  
Adsorption Process ◽  
Sorption Process ◽  
Multiwalled Carbon ◽  
Before And After ◽  
Kinetic Sorption

In this study, non-irradiated and weathered multiwalled carbon nanotubes (MWCNTs) obtained through irradiation, were studied as adsorbents for BPA, both nanomaterials being characterized before and after the adsorption process. The objectives of our investigation were to compare the characteristics of non-irradiated and irradiated MWCNTs, to evaluate the adsorption capacity of BPA by pristine and irradiated MWCNTs and to determine the variation of the kinetic, sorption and thermodynamic parameters during sorption process using both sorbents.

scholarly journals Enhanced Adsorption of Bisphenol A from Aqueous Solution with 2-Vinylpyridine Functionalized Magnetic Nanoparticles

Polymers ◽  
2018 ◽  
Vol 10 (10) ◽  
pp. 1136 ◽  
Author(s):  
Qiang Li ◽  
Fei Pan ◽  
Wentao Li ◽  
Dongya Li ◽  
Haiming Xu ◽  
...  
Keyword(s):  
Bisphenol A ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Magnetic Nanoparticle ◽  
Maximum Adsorption Capacity ◽  
Salting Out ◽  
Functionalized Magnetic Nanoparticles ◽  
Ft Ir ◽  
Fe3o4 Nanospheres ◽  
Enhanced Adsorption

In this study, a novel 2-vinylpyridine functionalized magnetic nanoparticle (Mag-PVP) was successfully prepared. The prepared Mag-PVP was characterized by transmission electronic microscopy (TEM), Fourier transform infrared spectrophotometry (FT-IR), vibrating sample magnetometry (VSM) and thermogravimetric analysis (TGA), and was used for the adsorption of bisphenol A (BPA) from aqueous solutions. Mag-PVP, which is composed of Fe3O4 nanoparticles and poly divinylbenzene-2-vinylpyridine (with a thickness of 10 nm), exhibited magnetic properties (Ms = 44.6 emu/g) and thermal stability. The maximum adsorption capacity (Qm) of Mag-PVP for BPA obtained from the Langmuir isotherm was 115.87 mg/g at 20 °C, which was more than that of Fe3O4 nanospheres. In the presence of NaCl, the improved adsorption capacity of Mag-PVP was probably attributed to the screening effect of Mag-PVP surface charge and salting-out effect. In the presence of CaCl2 and humic acid (HA), the adsorption capacity of BPA decreased due to competitive adsorption. The adsorption of BPA by Mag-PVP increased slightly with the increase in pH from 3.0 to 5.0 and obtained the largest adsorption amount at pH 5.0, which was probably attributed to hydrogen bonding interactions. Moreover, in actual water, Mag-PVP still showed excellent adsorption performance in removing BPA. The high adsorption capacity and excellent reusability performance in this work indicated that Mag-PVP was an effective adsorbent for removing BPA from aqueous solutions.

scholarly journals Mixed Oxide Layered Double Hydroxide Materials: Synthesis, Characterization and Efficient Application for Mn2+ Removal from Synthetic Wastewater

Materials ◽  
2020 ◽  
Vol 13 (18) ◽  
pp. 4089
Author(s):  
Cristina Modrogan ◽  
Simona Cǎprǎrescu ◽  
Annette Madelene Dǎncilǎ ◽  
Oanamari Daniela Orbuleț ◽  
Eugeniu Vasile ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Layered Double Hydroxides ◽  
Synthetic Wastewater ◽  
Precipitation Method ◽  
Metallic Ions ◽  
Materials Synthesis ◽  
Experimental Conditions ◽  
Edx Analysis ◽  
Co Precipitation ◽  
Double Hydroxides

Magnesium–aluminum (Mg-Al) and magnesium–aluminum–nickel (Mg-Al-Ni) layered double hydroxides (LDHs) were synthesized by the co-precipitation method. The adsorption process of Mn2+ from synthetic wastewater was investigated. Formation of the layered double hydroxides and adsorption of Mn2+ on both Mg-Al and Mg-Ni-Al LDHs were observed by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy Dispersive Spectrometry (EDX) analysis. XRD patterns for prepared LDHs presented sharp and symmetrical peaks. SEM studies revealed that Mg-Al LDH and Mg-Al-Ni LDH exhibit a non-porous structure. EDX analysis showed that the prepared LDHs present uniformly spread elements. The adsorption equilibrium on these LDHs was investigated at different experimental conditions such as: Shaking time, initial Mn2+ concentration, and temperatures (10 and 20 °C). The parameters were controlled and optimized to remove the Mn2+ from synthetic wastewater. Adsorption isotherms of Mn2+ were fitted by Langmuir and Freundlich models. The obtained results indicated that the isotherm data fitted better into the Freundlich model than the Langmuir model. Adsorption capacity of Mn2+ gradually increased with temperature. The Langmuir constant (KL) value of Mg-Al LDH (0.9529 ± 0.007 L/mg) was higher than Mg-Al-Ni LDH (0.1819 ± 0.004 L/mg), at 20 °C. The final adsorption capacity was higher for Mg-Al LDH (91.85 ± 0.087%) in comparison with Mg-Al-Ni LDH (35.97 ± 0.093%), at 20 °C. It was found that the adsorption kinetics is best described by the pseudo-second-order model. The results indicated that LDHs can be considered as a potential material for adsorption of other metallic ions from wastewater.

scholarly journals Magnetically Recyclable Wool Keratin Modified Magnetite Powders for Efficient Removal of Cu2+ Ions from Aqueous Solutions

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1068
Author(s):  
Xinyue Zhang ◽  
Yani Guo ◽  
Wenjun Li ◽  
Jinyuan Zhang ◽  
Hailiang Wu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Ion Concentration ◽  
Bet Surface Area ◽  
Chemical Compositions ◽  
Ion Adsorption ◽  
X Ray ◽  
Wool Keratin

The treatment of wastewater containing heavy metals and the utilization of wool waste are very important for the sustainable development of textile mills. In this study, the wool keratin modified magnetite (Fe3O4) powders were fabricated by using wool waste via a co-precipitation technique for removal of Cu2+ ions from aqueous solutions. The morphology, chemical compositions, crystal structure, microstructure, magnetism properties, organic content, and specific surface area of as-fabricated powders were systematically characterized by various techniques including field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM), thermogravimetric (TG) analysis, and Brunauer–Emmett–Teller (BET) surface area analyzer. The effects of experimental parameters such as the volume of wool keratin hydrolysate, the dosage of powder, the initial Cu2+ ion concentration, and the pH value of solution on the adsorption capacity of Cu2+ ions by the powders were examined. The experimental results indicated that the Cu2+ ion adsorption performance of the wool keratin modified Fe3O4 powders exhibited much better than that of the chitosan modified ones with a maximum Cu2+ adsorption capacity of 27.4 mg/g under favorable conditions (0.05 g powders; 50 mL of 40 mg/L CuSO4; pH 5; temperature 293 K). The high adsorption capacity towards Cu2+ ions on the wool keratin modified Fe3O4 powders was primarily because of the strong surface complexation of –COOH and –NH2 functional groups of wool keratins with Cu2+ ions. The Cu2+ ion adsorption process on the wool keratin modified Fe3O4 powders followed the Temkin adsorption isotherm model and the intraparticle diffusion and pseudo-second-order adsorption kinetic models. After Cu2+ ion removal, the wool keratin modified Fe3O4 powders were easily separated using a magnet from aqueous solution and efficiently regenerated using 0.5 M ethylene diamine tetraacetic acid (EDTA)-H2SO4 eluting. The wool keratin modified Fe3O4 powders possessed good regenerative performance after five cycles. This study provided a feasible way to utilize waste wool textiles for preparing magnetic biomass-based adsorbents for the removal of heavy metal ions from aqueous solutions.

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