scholarly journals Removal of lithium from water by aminomethylphosphonic acid-containing resin

2018 ◽  
Vol 83 (9) ◽  
pp. 1059-1069 ◽  
Author(s):  
Aydin Çiçek ◽  
Onur Yilmaz ◽  
Özgür Arar

This study gives an overview of the ability of aminomethylphosphonic acid containing chelating resin for the removal of lithium (Li+) from water. Studies were performed under various conditions such as resin dose, initial Li+ concentration, solution pH and solution temperature. Results showed that the sorption of Li+ reached equilibrium within 15 min and the experimental data were well fitted by the pseudo-second-order kinetic model. The Li+ sorption was highly pH dependent, and the optimum pH for Li+ removal was ?3. Isotherm sorption data displayed good correlation with the Langmuir model, and maximum monolayer sorption capacity of resin found as 13.65 mg/g. Thermodynamic studies suggested that Li+ sorption onto chelating resin was an exothermic and spontaneous process in nature. Resin can be regenerated by 0.1 M HCl, NaCl or H2SO4 with > 99 % efficiency. Desorption of Li+ with 0.1 M NaCl resulted in no changes of the uptake capacity through four subsequent sorption/desorption cycles

Metals ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 149
Author(s):  
Chunhui Zheng ◽  
Chunlin He ◽  
Yingjie Yang ◽  
Toyohisa Fujita ◽  
Guifang Wang ◽  
...  

The continuous expansion of the market demand and scale of commercial amidoxime chelating resins has caused large amounts of resin to be discarded around the world. In this study, the waste amidoxime chelating resin was reutilized as an adsorbent for the removal and recovery of Pb(II), Cu(II), Cd(II) and Zn(II) ions from aqueous solutions. The physical morphology and chemical composition of the waste amidoxime chelating resin (WAC-resin) from the factory was characterized by the elemental analyzer, X-ray photoelectron spectroscopy and Fourier-transform infrared spectroscopy. The influence of the initial metal ions concentration, contact time, temperature and the solution pH on the adsorption performance of the metal ions was explored by batch experiments. It was shown that the optimal pH was 4. Kinetic studies revealed that adsorption process corresponded with the pseudo-second-order kinetic model and the adsorption isotherm was consistent with the Langmuir model. At room temperature, the adsorption capacities of WAC-resin for Pb2+, Cu2+, Zn2+ and Cd2+ reached 114.6, 93.4, 24.4 and 20.7 mg/g, respectively.


2018 ◽  
Vol 21 (8) ◽  
pp. 583-593 ◽  
Author(s):  
Sara Rahnama ◽  
Shahab Shariati ◽  
Faten Divsar

Objective: In this research, a novel magnetite titanium dioxide nanocomposite functionalized by amine groups (Fe3O4@SiO2@TiO2-NH2) was synthesized and its ability for efficient removal of Acid Fuchsine as an anionic dye from aqueous solutions was investigated. Method: The core-shell structure of Fe3O4@SiO2@TiO2 was prepared using Fe3O4 as magnetic core, tetra ethyl orthosilicate as silica and tetra butyl titanate as titanium source for shell. The synthesized nanocomposites (particle size lower than 44 nm) were characterized by FT-IR, XRD, DRS, SEM and TGA instruments. The various experimental parameters affecting dye removal efficiency were investigated and optimized using Taguchi fractional factorial design. Results: The synthesized adsorbent showed the highest removal efficiency of Acid Fuchsine (99 %) at pH= 3.5, without salt addition and during stirring at contact times less than 10 minutes. The study of kinetic models at two concentration levels showed the fast dye sorption on the surface of proposed nanocomposites with pseudo second order kinetic model (R2=1). Also, the fitting of Acid Fuchsine sorption data to Freundlich, Langmuir and Temkin isotherms suggested that Freundlich model gave a better fitting than other models (R2=0.9936, n=2). Conclusion: Good chemical stability, excellent magnetic properties, very fast adsorption kinetics and high removal efficiency make the synthesized nanocomposite as a proper recoverable sorbent for removal of Acid Fuchsine dye from wastewaters.


2017 ◽  
Vol 75 (6) ◽  
pp. 1500-1511 ◽  
Author(s):  
Shengjiong Yang ◽  
Pengkang Jin ◽  
Xiaochang C. Wang ◽  
Qionghua Zhang ◽  
Xiaotian Chen

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.


2011 ◽  
Vol 6 (3) ◽  
pp. 155892501100600 ◽  
Author(s):  
Fang Li ◽  
Chunmei Ding

Different degree of deacetylation (DD) chitosan was prepared and used for the removal of a Reactive black M-2R (RBM) from aqueous solution. The effects of temperature (298 K~323 K), chitosan dosage, degree of deacetylation on RBM removal were investigated. The adsorption equilibrium was reached within one hour. In order to determine the adsorption capacity, the sorption data were analyzed by using linear form of Langmuir, Freundlich and Tempkin isotherm equation. Langmuir equation shows higher conformity than the other two equations. From the kinetic experiment data, it was found that the sorption process follows the pseudo-second-order kinetic model. Activation energy value for sorption process was found to be 58.28 kJ mol-1. Chitosan with 66% deacetylation degree (DD) exhibited good adsorption performance for RBM. In order to determine the interactions between RBM and chitosan, FTIR analysis was also conducted.


Author(s):  
Xiaochun Yin ◽  
Nadi Zhang ◽  
Meixia Du ◽  
Hai Zhu ◽  
Ting Ke

Abstract In this paper, a series of bio-adsorbents (LR-NaOH, LR-Na2CO3 and LR-CA) were successfully prepared by modifying Licorice Residue with NaOH, Na2CO3 and citric acid, which were used as the adsorbents to remove Cu2+ from wastewater. The morphology and structure of bio-adsorbents were characterized by Fourier Transform Infrared, SEM, TG and XRD. Using static adsorption experiments, the effects of the adsorbent dosage, the solution pH, the adsorption time, and the initial Cu2+ concentration on the adsorption performance of the adsorbents were investigated. The results showed that the adsorption process of Cu2+ by the bio-adsorbents can be described by pseudo-second order kinetic model and the Langmuir model. The surface structure of the LR-NaOH, LR-Na2CO3 and LR-CA changed obviously, and the surface-active groups increased. The adsorption capacity of raw LR was 21.56 mg/g, LR-NaOH, LR- Na2CO3 significantly enhanced this value up to 43.65 mg/g, 43.55 mg/g, respectively. After four adsorption-desorption processes, the adsorption capacity of LR-NaOH also maintained about 73%. Therefore, LR-NaOH would be a promising adsorbent for removing Cu2+ from wastewater, and the simple strategy towards preparation of adsorbent from the waste residue can be as a potential approach using in the water treatment.


2020 ◽  
Vol 10 (9) ◽  
Author(s):  
G. B. Adebayo ◽  
H. I. Adegoke ◽  
Sidiq Fauzeeyat

Abstract Hexavalent chromium was adsorbed from aqueous solution with three prepared and characterized adsorbents, namely goethite (G), activated carbon (AC) and their composite (GAC). The goethite particle was synthesized using the precipitation methods, and activated carbon was prepared from the stem bark of Daniellia oliveri tree and composite in a ratio of 1:5 goethite–activated carbon. The adsorption capacities of G, AC and GAC for Cr(VI) are 6.627, 5.455 and 6.354 mg/g with 0.02 g adsorbent within contact time of 60, 180 and 30 min for G, AC and GAC, respectively, for Cr(VI) adsorption at optimum pH of 3. The isotherm studied was best explained by Langmuir adsorption isotherm and fitted with the pseudo-second-order kinetic model. Desorption studies showed that 1.0 M HNO3 was a better desorbing agent than 0.1 M HNO3, 0.1 M HCl and 1.0 M HCl. Chromium was most desorbed (94.60% in Cr//G using 1 M HNO3). The result obtained revealed that goethite and activated carbon produced are favourable adsorbents and the composite of the two adsorbents gives a more favourable, economical and affordable adsorbent for the clean-up of heavy metal contamination.


Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil

The sorption of uranium and thorium from their aqueous solutions by using 8-hydroxyquinoline modified Na-bentonite (HQ-bentonite) was investigated by the batch technique. Na-bentonite and HQ-bentonite were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier Transform Infrared (FTIR) spectroscopy. Factors that influence the sorption of uranium and thorium onto HQ-bentonite such as solution pH, contact time, initial metal ions concentration, HQ-bentonite mass, and temperature were tested. Sorption experiments were expressed by Freundlich and Langmuir isotherms and the sorption results demonstrated that the sorption of uranium and thorium onto HQ-bentonite correlated better with the Langmuir isotherm than the Freundlich isotherm. Kinetics studies showed that the sorption followed the pseudo-second-order kinetic model. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° indicated that the sorption of uranium and thorium onto HQ-bentonite was endothermic, feasible, spontaneous, and physical in nature. The maximum adsorption capacities of HQ-bentonite were calculated from the Langmuir isotherm at 303 K and were found to be 63.90 and 65.44 for U(VI) and Th(IV) metal ions, respectively.


2017 ◽  
Vol 8 (4) ◽  
pp. 522-531
Author(s):  
A. Machrouhi ◽  
M. Farnane ◽  
A. Elhalil ◽  
R. Elmoubarki ◽  
M. Abdennouri ◽  
...  

Abstract Raw beetroot seeds (BS) and H3PO4 activated beetroot seeds (H3PO4-BS) were evaluate for their effectiveness in removing methylene blue (MB) and malachite green (MG) from aqueous solution. BS were carbonized at 500°C for 2 h, and then impregnated with phosphoric acid (phosphoric acid to BS ratio of 1.5 g/g). The impregnated BS were activated in a tubular vertical furnace at 450°C for 2 h. Batch sorption experiments were carried out under various parameters, such as solution pH, adsorbent dosage, contact time, initial dyes concentration and temperature. The experimental results show that the dye sorption was influenced by solution pH and it was greater in the basic range. The sorption yield increases with an increase in the adsorbent dosage. The equilibrium uptake was increased with an increase in the initial dye concentration in solution. Adsorption kinetic data conformed more to the pseudo-second-order kinetic model. The experimental isotherm data were evaluated by Langmuir, Freundlich, Toth and Dubinin–Radushkevich isotherm models. The Langmuir maximum monolayer adsorption capacities were 61.11 and 74.37 mg/g for MB, 51.31 and 213.01 mg/g for MG, respectively in the case of BS and H3PO4-BS. The thermodynamic parameters are also evaluated and discussed.


2010 ◽  
Vol 62 (8) ◽  
pp. 1888-1897 ◽  
Author(s):  
Nan Chen ◽  
Zhenya Zhang ◽  
Chuanping Feng ◽  
Miao Li ◽  
Rongzhi Chen ◽  
...  

Kanuma mud, a geomaterial, is used as an adsorbent for the removal of fluoride from water. The influences of contact time, solution pH, adsorbent dosage, initial fluoride concentration and co-existing ions were investigated by batch equilibration studies. The rate of adsorption was rapid with equilibrium being attained after about 2 h, and the maximum removal of fluoride was obtained at pH 5.0–8.0. The Freundlich isotherm model was found to represent the measured adsorption data well. The negative value of the thermodynamic parameter ΔG suggests the adsorption of fluoride by Kanuma mud was spontaneous, the endothermic nature of adsorption was confirmed by the positive ΔH value. The negative ΔS value for adsorbent denoted decreased randomness at the solid/liquid interface. The adsorption process using Kanuma mud followed the pseudo-second-order kinetic model. Fluoride uptake by the Kanuma mud was a complex process and intra-particle diffusion played a major role in the adsorption process. It was found that adsorbed fluoride could be easily desorbed by washing the adsorbent with a solution of pH 12. This indicates the material could be easily recycled.


2014 ◽  
Vol 931-932 ◽  
pp. 286-290 ◽  
Author(s):  
W. Pimpa ◽  
C. Pimpa

The intention of this study was to prepare the environment friendly durian seed starch/polyvinyl alcohol (DSS/PVOH) composite hydrogels modified by chemical cross-linking with glutaraldehyde and to assess the adsorption potential of the DSS/PVOH composite hydrogels for the removal of the synthetic dyes from aqueous solution. The hydrogels were characterized by swelling behavior and scanning electron microscope (SEM). The effect of DSS content and initial dye solution pH on the adsorption capacity was studied conducting batch experiment system. The DSS/PVOH composite hydrogels consisting 3% DSS has optimum adsorption capacity of 3.411 mg/g (for methylene blue under the condition of pH 7) and 3.274 mg/g (for acid orange 8 under the condition of pH 2.5) at 24 h of contact time. The adsorptions were well fitted by the pseudo-second order kinetic model. It was indicated that the mechanism of removal predominant is effective for low dye concentrations, below 10 mg/l.


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