scholarly journals Uranium biosorption from aqueous solution by the submerged aquatic plant Hydrilla verticillata

2016 ◽  
Vol 75 (6) ◽  
pp. 1332-1341 ◽  
Author(s):  
Zheng-ji Yi ◽  
Jun Yao ◽  
Mi-jia Zhu ◽  
Hui-lun Chen ◽  
Fei Wang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Aquatic Macrophyte ◽  
Hydrilla Verticillata ◽  
Hydroxyl Groups ◽  
Order Kinetic ◽  
Experimental Conditions ◽  
Submerged Aquatic Plant ◽  
Isotherm Adsorption ◽  
Order Kinetic Model

The biosorption characteristics of U(VI) from aqueous solution onto a nonliving aquatic macrophyte, Hydrilla verticillata (dry powder), were investigated under various experimental conditions by using batch methods. Results showed that the adsorption reached equilibrium within 60 min and the experimental data were well fitted by the pseudo-first-order kinetic model. U(VI) adsorption was strongly pH dependent, and the optimum pH for U(VI) removal was 5.5. Isotherm adsorption data displayed good correlation with the Langmuir model, with a maximum monolayer adsorption capacity of 171.52 mg/g. Thermodynamic studies suggested that U(VI) adsorption onto H. verticillata was an exothermic and spontaneous process in nature. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy indicated that the amino and hydroxyl groups on the algal surface played an important role in U(VI) adsorption. The mechanisms responsible for U(VI) adsorption could involve electrostatic attraction and ion exchange. In conclusion, H. verticillata biomass showed good potential as an adsorption material for the removal of uranium contaminants in aqueous solution.

Biosorption of hexavalent chromium from aqueous solution by polyethyleneimine-modified ultrasonic-assisted acid hydrochar from Sargassum horneri

2020 ◽  
Vol 81 (6) ◽  
pp. 1114-1129 ◽  
Author(s):  
Jun Wang ◽  
Qinglong Xie ◽  
Ao Li ◽  
Xuejun Liu ◽  
Fengwen Yu ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Batch Adsorption ◽  
Crosslinking Reaction ◽  
Order Kinetic ◽  
Adsorption Capacities ◽  
Initial Ph ◽  
Ultrasonic Assisted ◽  
Order Kinetic Model ◽  
Pseudo Second Order

Abstract In this study, an efficient route to synthesizing polyethyleneimine-modified ultrasonic-assisted acid hydrochar (PEI-USAH) is developed and reported. Ultrasonic irradiation technique was used as surface modification method to shorten the crosslinking reaction for hydrochar and polyethyleneimine (PEI). The PEI-USAH showed an excellent adsorption capacity for Cr(VI) from aqueous solution. The physicochemical properties of this PEI-modified adsorbent were comparatively characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, Brunauer–Emmett–Teller analysis and CNHS analysis. The effects of contact time, initial pH, and biosorbent dose on adsorption capacities were investigated. The batch adsorption experiments showed that PEI-USAH possessed the maximum adsorption capacities of 94.38 mg/g and 330.84 mg/g for initial Cr(VI) concentration of 100 mg/L and 500 mg/L, respectively. Furthermore, this adsorption process could be fitted to Langmuir adsorption and described by the pseudo second order kinetic model. Based on the above findings, PEI-USAH could be used as a potential adsorbent for removal of Cr(VI) from wastewater.

scholarly journals On the Active Adsorption of Chromium(III) from Alkaline Solutions Using Multi-Walled Carbon Nanotubes

2019 ◽  
Author(s):  
Francisco J. Alguacil ◽  
Félix A. López
Keyword(s):  
Carbon Nanotubes ◽  
Aqueous Solution ◽  
Alkaline Media ◽  
Alkaline Solutions ◽  
Order Kinetic ◽  
Experimental Conditions ◽  
Equilibrium Data ◽  
Order Kinetic Model ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes

The present investigation deals with the adsorption of chromium(III) from alkaline media using multi-walled carbon nanotubes. The adsorption of Cr(III) has been studied under various experimental conditions: stirring speed of the aqueous solution, initial metal and adsorbent concentrations, NaOH concentration in the aqueous solution, and temperature. The rate law indicated that chromium adsorption is well represented by the particle diffusion model, whereas the adsorption process fits to the pseudo-second order kinetic model within an exothermic character. Equilibrium data fit to the Langmuir type-2 equilibrium isotherm in an spontaneous process. Chromium(III) can be eluted from metal-loaded nanotubes using acidic solutions, from which fine chromium(III) oxide pigment can be ultimately yielded.

scholarly journals Adsorption of Co(II) from aqueous solution using municipal sludge biochar modified by HNO3

2021 ◽  
Author(s):  
Chunlian Hu ◽  
Wei Zhang ◽  
Yuantao Chen ◽  
Na Ye ◽  
DaWa YangJi ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Order Kinetic ◽  
Adsorption Effect ◽  
Surface Areas ◽  
Order Kinetic Model ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Adsorption Of Co

Abstract Herein adsorption studies were proposed on a carboxylated sludge biochar (CSB) material modified by HNO3 to assess its capacity in the removal of cobalt from aqueous solution. The as-prepared sludge biochar material were characterized by Brunaure-Emmett-Teller (BET), Fourier transform infrared (FT-IR), Thermogravimetric analysis (TGA), Energy-dispersive spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). The isotherm process could be well described by Langmuir isotherm model. The adsorption kinetics indicated that cobalt adsorption followed pseudo-second-order kinetic model. The mechanism between Co(II) and biochar involved electrostatic interaction, ion exchange, surface complexation and physical function. The adsorption capacity on CSB was as high as 72.27 mg·g−1, surpassing original sludge biochar (SB). This is due to the fact that CSB had abundant oxygen-containing functional groups and many hydroxyls, as well as, the BET surface areas increased when SB was modified by HNO3, which stimulate adsorption effect. Therefore, this work shows that CSB could be used as an efficient adsorbent to remove Co(II) in the wastewater.

scholarly journals On the Active Adsorption of Chromium(III) from Alkaline Solutions Using Multiwalled Carbon Nanotubes

2019 ◽  
Vol 10 (1) ◽  
pp. 36 ◽  
Author(s):  
Francisco José Alguacil ◽  
Félix A. López
Keyword(s):  
Carbon Nanotubes ◽  
Aqueous Solution ◽  
Multiwalled Carbon Nanotubes ◽  
Alkaline Media ◽  
Alkaline Solutions ◽  
Order Kinetic ◽  
Multiwalled Carbon ◽  
Experimental Conditions ◽  
Equilibrium Data ◽  
Order Kinetic Model

The present investigation deals with the adsorption of chromium(III) from alkaline media, as representative of highly-caustic component solutions of nuclear tank wastes, using multiwalled carbon nanotubes. The adsorption of Cr(III) has been studied under various experimental conditions, i.e., stirring speed of the aqueous solution, initial metal and adsorbent concentrations, NaOH concentration in the aqueous solution, and temperature. The rate law indicated that chromium adsorption is well represented by the particle diffusion model, whereas the adsorption process fits with the pseudo-second order kinetic model within an exothermic setting. Equilibrium data fit to the Langmuir type-2 equilibrium isotherm in a spontaneous process. Chromium(III) can be eluted from metal-loaded nanotubes using acidic solutions, from which fine chromium(III) oxide pigment can ultimately be yielded.

scholarly journals Adsorption of Benzene by “Green” functionalization of Montmorillonite

2018 ◽  
Vol 150 ◽  
pp. 02001 ◽  
Author(s):  
Hirra Anjum ◽  
Mansoor Abdullah Obaid ◽  
Muhammad Yasir Shamim ◽  
Thanabalan Murugesan
Keyword(s):  
Aqueous Solution ◽  
Batch Process ◽  
Morphological Properties ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Experimental Conditions ◽  
Organically Modified ◽  
Order Kinetic Model ◽  
Mmt Clay ◽  
Nonpolar Organic

The capacity of organically modified Montmorillonite (MMT) clay to adsorb nonpolar organic compound (benzene) in an aqueous solution, was investigated under the batch process. MMT was pretreated (centrifuged) and then functionalized with green intercalating agent i.e. 1-hexyl-3-methyl imadazolium chloride [HMim][Cl]. The characterization through Fourir Transoform Infrared Spectroscopy (FTIR), Differential Scanning Calorimeter (DSC) and Field Emission Scanning Electron Microscope (FE-SEM) confirmed the presence of the oxygen containing functional groups, changes in melting point and variation in the morphological properties. The governing parameters for the sorption of benzene such as the effect of contact time, pH, adsorbent dose and rotation were studied. The kinetic data conformed to pseuodo 2nd order kinetic model and the isotherm experimental data were a better fit to Langmuir model with maximum adsorption capacity of 588.23mg/g under experimental conditions. Overall, MMT intercalated with 1-hexyl-3-methyl imadazolium chloride is a promising environmental friendly adsorbent for the abatement of benzene in an aqueous solution.

scholarly journals Modification of Cu/Cr Layered Double Hydroxide by Keggin Type Polyoxometalate as Adsorbent of Malachite Green from Aqueous Solution

2021 ◽  
Vol 6 (3) ◽  
pp. 209-217
Author(s):  
Neza Rahayu Palapa ◽  
Tarmizi Taher ◽  
Alfan Wijaya ◽  
Aldes Lesbani
Keyword(s):  
Aqueous Solution ◽  
Malachite Green ◽  
Adsorption Process ◽  
Order Kinetic ◽  
Keggin Type ◽  
Isotherm Adsorption ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Double Hydroxide ◽  
Double Hydroxides

Modification of Cu/Cr layered double hydroxides (LDHs) has been conducted by intercalation using Keggin type polyoxometalate [a-SiW12O40]4- to form CuCr-[a-SiW12O40]. The materials were analyzed by XRD, FTIR, and surface area analyses. Furthermore, materials were used as selectivity adsorbents of cationic dyes such as malachite green, rhodamine-B and methylene blue. The malachite green is more selective than others from an aqueous solution. The adsorption of malachite green showed that the adsorption capacity of CuCr-[a-SiW12O40] was higher than pristine LDHs. The adsorption process was followed pseudo second order kinetic model and Langmuir isotherm adsorption. The Qmax value of CuCr-[a-SiW12O40] reached 55.322 mg/g at 323 K after 100 minutes adsorption time. Thermodynamic parameters such as ΔG, ΔH and ΔS confirm that the adsorption process was endothermic, spontaneous, and more favorable at high temperatures. The intercalated material was higher structural stability toward reusability adsorbent than pristine LDHs.

scholarly journals Facile Synthesis of Polyethylene Glycol@Tannin-Amine Microsphere towards Cr(VI) Removal

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1035
Author(s):  
Chengbing Yuan ◽  
Yan Zhang ◽  
Jinshui Yao ◽  
Qinze Liu ◽  
Fan-Gong Kong
Keyword(s):  
Polyethylene Glycol ◽  
Adsorption Capacity ◽  
Photoelectron Spectroscopy ◽  
Sewage Treatment ◽  
Maximum Adsorption Capacity ◽  
Hydroxyl Groups ◽  
Order Kinetic ◽  
Initial Concentration ◽  
Synthetic Strategy ◽  
Order Kinetic Model

Herein, a synthetic strategy for a rough microsphere Cr(VI)-adsorbent via the reaction of tannic acid (TA) and 1,6-hexanediamine (HA) and using polyethylene glycol (PEG) as surface modifier was presented. This adsorbent was characterized by a Fourier Transform Infrared spectrometer (FTIR), thermogravimetic analysis (TGA), X-ray photoelectron spectroscopy (XPS), etc. Certain factors, including contact time, PEG@poly(tannin-1,6-hexanediamine) (PEG@PTHA) dosage, initial concentration, and experimental temperature affecting the Cr(VI) adsorption performance of adsorbent were explored. PEG@PTHA can adsorb Cr and the Cr(VI) was reduced up to Cr(III) due to the existence of phenolic hydroxyl groups. Its adsorption capacity can reach up to 300 mg/g within 10 min and approximately 100% removal percentage below the initial concentration of 100 mg/L. Its behavior matched well with the Langmuir isotherm model and pseudo-second-order kinetic model. A PEG@PTHA adsorbent with maximum adsorption capacity (450 mg/g) has great prospects in Cr(VI)-sewage treatment.

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.

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.

Performance of poly-o-phenylenediamine and its carbon dot composite electrode in the removal of Cu2+ from its aqueous solution

2021 ◽  
pp. 2151037
Author(s):  
Yu Meng ◽  
Qing Zhong ◽  
Arzugul Muslim
Keyword(s):  
Aqueous Solution ◽  
Electrochemical Reduction ◽  
Composite Electrode ◽  
Reduction Process ◽  
Order Kinetic ◽  
Carbon Dot ◽  
First Order ◽  
Oxidation Reduction ◽  
Order Kinetic Model ◽  
Optimal Ph

Because −NH2 and −NH− in poly-[Formula: see text]-phenylenediamine (P[Formula: see text]PD) can interact strongly with the empty orbitals of Cu to show unique electrochemical activity, P[Formula: see text]PD is suitable for the removal of Cu[Formula: see text] by electrochemical oxidation–reduction process. In this study, with P[Formula: see text]PD and its carbon dot composite (CDs/P[Formula: see text]PD) as working electrodes, the electrochemical reduction and removal of Cu[Formula: see text] in the aqueous solution were carried out with the potentiostatic method. According to effects of voltage, pH of the solution, initial concentration of Cu[Formula: see text], and electrochemical reduction time on the Cu[Formula: see text] removal, the Cu[Formula: see text] removal ratios of P[Formula: see text]PD and CDs/P[Formula: see text]PD were up to 64.69% and 73.34%, respectively, at −0.2 V and the optimal pH. Additionally, results showed that these processes were in line with the quasi-first order kinetic model. Both P[Formula: see text]PD and CDs/P[Formula: see text]PD showed good reproducibility in six cycles. After five times of repeated usage, the regeneration efficiencies of P[Formula: see text]PD and CDs/P[Formula: see text]PD dropped to 77.04% and 79.36%, respectively.

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