Gold Recovery from Aqueous Solutions Using Bioadsorbent Synthesized from Rambutan Peel

2012 ◽  
Vol 506 ◽  
pp. 405-408 ◽  
Author(s):  
T. Rubcumintara ◽  
A. Aksornpan ◽  
W. Jonglertjunya ◽  
W. Koo-Amornpattana ◽  
P. Tasaso
Keyword(s):  
Gold Recovery ◽  
Hydroxyl Groups ◽  
Loading Capacity ◽  
Order Kinetic ◽  
Gold Concentration ◽  
Solution Ph ◽  
Adsorbent Surface ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ft Ir

The recovery of gold from chloride solutions using bioadsorbent synthesized from waste rambutan peel was studied. The initial gold concentration 25-900 mg/L, solution pH 1-4, temperature 25-60 °C and the amount of adsorbent 1-25 mg were found to affect the efficiency for gold recovery as well as loading capacity. The 99.8 % gold recovery was accomplished in 1 h with loading capacity of 100 mg Au/g adsorbent at the following conditions: adsorbent 25 mg, initial gold concentration 100 mg/L, pH 2 and temperature 60 °C. The decrease of adsorbent from 25 to 1 mg resulted in the highest loading capacity of 2530 mg Au/g adsorbent and 100 % gold recovery within 100 h. The adsorption isotherm as well as mechanism were also elucidated. The Langmuir isotherm and the pseudo second-order kinetic model were fitted well with the experimental results. The activation energy of reaction was calculated to be 31.07 kJ/mol. The mechanism of adsorption is clarified to be the oxidation of hydroxyl groups and reduction of trivalent gold ions to metallic gold on the adsorbent surface which were supported by FT-IR, XRF and SEM.

Synthesis of Functionalized Magnetite Titanium Dioxide Nanocomposite for Removal of Acid Fuchsine Dye

2018 ◽  
Vol 21 (8) ◽  
pp. 583-593 ◽  
Author(s):  
Sara Rahnama ◽  
Shahab Shariati ◽  
Faten Divsar
Keyword(s):  
Titanium Dioxide ◽  
Removal Efficiency ◽  
Magnetic Core ◽  
Fractional Factorial ◽  
Order Kinetic ◽  
Sorption Data ◽  
Salt Addition ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ft Ir

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.

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.

REMOVAL OF STRONTIUM (II) FROM AQUEOUS SOLUTION USING FUNCTIONALIZED CARBON NANOTUBES

2012 ◽  
Vol 11 (02) ◽  
pp. 1250019 ◽  
Author(s):  
RAJESH KUMAR ◽  
S. K. JAIN
Keyword(s):  
Carbon Nanotubes ◽  
Polluted Water ◽  
Order Kinetic ◽  
Environmental Application ◽  
Functionalized Carbon Nanotubes ◽  
Multi Wall Carbon Nanotubes ◽  
Adsorption Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ft Ir

This study was carried out to evaluate the environmental application of functionalized carbon nanotubes through the experimental removal of strontium (II) from water. The aim was to find the optimal condition for the removal of strontium from water under different conditions such as initial concentration of strontium, contact time and neutral pH. The functionalized multi wall carbon nanotubes (f-MWCNT) were characterized by FT-IR and scanning electron microscopy (SEM). The adsorption isotherms were correlated to Freundlich and Langmuir models and it was found that the adsorption data could be fitted better by Langmuir model than Freundlich one. The kinetic data shows that the adsorption describes well with the pseudo-second order kinetic model. Functionalized MWCNT can be used as good adsorbent for the removal of the strontium ions from polluted water according to results.

Adsorption of Zn(II) from Aqueous Solutions by Thiol-Functionalized MCM-48

2011 ◽  
Vol 413 ◽  
pp. 148-153 ◽  
Author(s):  
Xue Na Hu ◽  
Ya Han ◽  
Jia Yan Li ◽  
Jun Yan Wu ◽  
Jian Rong Chen ◽  
...  
Keyword(s):  
Ethylene Oxide ◽  
Batch Adsorption ◽  
Order Kinetic ◽  
Pluronic P123 ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Poly Ethylene Oxide ◽  
Ft Ir ◽  
Poly Ethylene ◽  
Poly Propylene

Thiol-functionalized MCM-48 (SH-MCM-48) was synthesized by co-condensation method, with co-templates of cetyltrimethylammonium bromide (CTAB) and nonionic poly (ethylene oxide)–poly (propylene oxide)–poly (ethylene oxide) triblock copolymer (Pluronic P123). The resulting material was characterized by XRD and FT-IR spectrum. The potential of SH-MCM-48 for adsorption Zn (II) from aqueous solution was examined. Batch adsorption studies were carried out to investigate the effect of experimental parameters including pH, metal ions concentration and adsorption time. The maximum adsorption capacities of Zn (II) onto SH-MCM-48 were 30.12, 34.01 and 38.02 mg g-1 at the temperature of 303, 313 and 323K, respectively. The adsorption kinetics data were found to follow the pseudo-second-order kinetic model, and adsorption isotherms were fitted well with Langmuir and Freundlich models. Moreover, the adsorption thermodynamic parameters (△G0, △H0 and △S0) were measured, and indicated that the adsorption was an exothermic and spontaneous process.

scholarly journals Karekterisasi, Kinetika, dan Isoterm Adsorpsi Limbah Ampas Kelapa sebagai Adsorben Ion Cu(II)

SAINTIFIK ◽  
2020 ◽  
Vol 6 (2) ◽  
pp. 104-115
Author(s):  
Agusriyadin Agusriyadin
Keyword(s):  
Adsorption Capacity ◽  
Ph Effect ◽  
Maximum Adsorption Capacity ◽  
Order Kinetic ◽  
Optimum Conditions ◽  
Langmuir Adsorption ◽  
Adsorbent Surface ◽  
Adsorption Data ◽  
Order Kinetic Model ◽  
Pseudo Second Order

Penelitian ini bertujuan untuk menguji kemampuan AK dan AKPM dalam mengadsorpsi ion Cu (II), pengaruh parameter adsorpsi dan mekanisme adsorpsi. AK dan AKP Madsorben dibuat dari residu ampas kelapa. Adsorben dikarakterisasi dengan FTIR, SEM dan EDS. Pengaruh parameter adsorpsi seperti pH awal, dosis adsorben, waktu kontak dan konsentrasi ion Cu (II) awal diperiksa untuk menentukan kondisi optimum serapan tembaga (II). Ion Cu (II) yang teradsorpsi diukur berdasarkan pada konsentrasi Ion Cu (II) sebelum dan sesudah adsorpsi menggunakan metode AAS. Hasil karakterisasi menunjukkan bahwa struktur pori dan gugus fungsi tersedia pada permukaan adsorben. Menurut percobaan efek pH, kapasitas adsorpsi maksimum dicapai pada pH 7. Waktu kontak optimal dan konsentrasi tembaga awal (II) ditemukan masing-masing pada 120 menit dan 100 mg L-1. Data eksperimental sesuai dengan model kinetik orde dua orde dua, dan Langmuir isoterm adsorpsi yang diperoleh paling sesuai dengan data adsorpsi. Kapasitas adsorpsi maksimum adsorben ditemukan menjadi 4,73 dan 6,46 mg g-1 pada kondisi optimal. The results of characterization showed that the pore structure and the functional groups were available on adsorbent surface. According to the pH effect experiments, the maximum adsorption capacity was achieved at pH 7. Optimum contact time and initial copper(II) concentration were found at 120 min and 100 mg L-1, respectively. The experimental data were comply with the pseudo-second-order kinetic model, and Langmuir adsorption isotherm obtained best fitted the adsorption data. The maximum adsorption capacity of the adsorbents was found to be 4.73 and 6.46 mg g-1 at optimum conditions.

scholarly journals Preparation of bio-absorbents by modifying licorice residue via chemical methods and removal of copper ions from wastewater

2021 ◽  
Author(s):  
Xiaochun Yin ◽  
Nadi Zhang ◽  
Meixia Du ◽  
Hai Zhu ◽  
Ting Ke
Keyword(s):  
Adsorption Capacity ◽  
Copper Ions ◽  
Order Kinetic ◽  
Solution Ph ◽  
Chemical Methods ◽  
Simple Strategy ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Surface Active ◽  
Adsorption Desorption

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.

scholarly journals The Removal of Uranium and Thorium from Their Aqueous Solutions by 8-Hydroxyquinoline Immobilized Bentonite

Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil
Keyword(s):  
Aqueous Solutions ◽  
Metal Ions ◽  
Langmuir Isotherm ◽  
Freundlich Isotherm ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
X Ray ◽  
Order Kinetic Model ◽  
Pseudo Second Order

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.

scholarly journals Preparation and Adsorption Properties of Biochar/g-C3N4 Composites for Methylene Blue in Aqueous Solution

2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Xiaodong Li
Keyword(s):  
Methylene Blue ◽  
Thermodynamic Parameters ◽  
Raw Materials ◽  
Order Kinetic ◽  
Adsorption Effect ◽  
Freundlich Model ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Doping Ratio

Using straw and urea as raw materials, biochar (BC) and g-C3N4 were prepared by oxygen-free pyrolysis at 300°C and 550°C. BC/g-C3N4 was prepared by loading different amounts of g-C3N4 onto the surface of biochar and characterized by SEM and FT-IR. The adsorption effect on methylene blue (MB) was investigated from the aspects of dosage and pH. The studies of adsorption equilibrium isotherms and the kinetic and the thermodynamic parameters on the BC/g-C3N4 adsorbents are discussed. The results showed that BC/g-C3N4 0.16 g/L with a doping ratio of 1 : 3 was added to the MB solution with an initial concentration of 50 mg/L and pH=11. The adsorption rate and adsorption amount were 96.72% and 302.25 mg/g, respectively. The adsorption process included surface adsorption and intraparticle diffusion, which conformed to the pseudo-second-order kinetic model and Langmuir-Freundlich model. Thermodynamic parameters (ΔG0<0, ΔH0>0, and ΔS0>0) showed that the adsorption reaction is spontaneous, which positively correlated with temperature.

scholarly journals Effectiveness of beetroot seeds and H3PO4 activated beetroot seeds for the removal of dyes from aqueous solutions

2017 ◽  
Vol 8 (4) ◽  
pp. 522-531
Author(s):  
A. Machrouhi ◽  
M. Farnane ◽  
A. Elhalil ◽  
R. Elmoubarki ◽  
M. Abdennouri ◽  
...  
Keyword(s):  
Phosphoric Acid ◽  
Isotherm Models ◽  
Order Kinetic ◽  
Solution Ph ◽  
Experimental Isotherm ◽  
Adsorbent Dosage ◽  
Adsorption Capacities ◽  
Monolayer Adsorption ◽  
Order Kinetic Model ◽  
Pseudo Second Order

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.

Removal of fluoride from aqueous solution by adsorption onto Kanuma mud

2010 ◽  
Vol 62 (8) ◽  
pp. 1888-1897 ◽  
Author(s):  
Nan Chen ◽  
Zhenya Zhang ◽  
Chuanping Feng ◽  
Miao Li ◽  
Rongzhi Chen ◽  
...  
Keyword(s):  
Adsorption Process ◽  
Fluoride Concentration ◽  
Freundlich Isotherm ◽  
Order Kinetic ◽  
Solution Ph ◽  
Intra Particle Diffusion ◽  
Order Kinetic Model ◽  
Pseudo Second Order ◽  
Solid Liquid Interface ◽  
Solid Liquid

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.

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