scholarly journals Characterization of Residual Biomasses and Its Application for the Removal of Lead Ions from Aqueous Solution

2019 ◽  
Vol 9 (21) ◽  
pp. 4486 ◽  
Author(s):  
Candelaria Tejada-Tovar ◽  
Angel Darío Gonzalez-Delgado ◽  
Angel Villabona-Ortiz

The removal of water pollutants has been widely addressed for the conservation of the environment, and novel materials are being developed as adsorbent to address this issue. In this work, different residual biomasses were employed to prepare biosorbents applied to lead (Pb(II)) ion uptake. The choice of cassava peels (CP), banana peels (BP), yam peels (YP), and oil palm bagasse (OPB) was made due to the availability of such biomasses in the Department of Bolivar (Colombia), derived from agro-industrial activities. The materials were characterized by ultimate and proximate analysis, Fourier Transform Infrared Spectroscopy (FTIR), Brunauer-Emmett-Teller analysis (BET), Scanning Electron Microscopy (SEM), and Energy Dispersive X-Ray Spectroscopy (EDS) in order to determine the physicochemical properties of bioadsorbents. The adsorption tests were carried out in batch mode, keeping the initial metal concentration at 100 ppm, temperature at 30 °C, particle size at 1 mm, and solution pH at 6. The experimental results were adjusted to kinetic and isotherm models to determine the adsorption mechanism. The remaining concentration of Pb(II) in solution was measured by atomic absorption at 217 nm. The functional groups identified in FTIR spectra are characteristic of lignocellulosic materials. A high surface area was found for all biomaterials with the exception of yam peels. A low pore volume and size, related to the mesoporous structure of these materials, make these bioadsorbents a suitable alternative for liquid phase adsorption, since they facilitate the diffusion of Pb(II) ions onto the adsorbent structure. Both FTIR and EDS techniques confirmed ion precipitation onto adsorbent materials after the adsorption process. The adsorption tests reported efficiency values above 80% for YP, BP, and CP, indicating a good uptake of Pb(II) ions from aqueous solution. The results reported that Freundlich isotherm and pseudo-second order best fit experimental data, suggesting that the adsorption process is governed by chemical reactions and multilayer uptake. The future prospective of this work lies in the identification of alternatives to reuse Pb(II)-contaminated biomasses after heavy metal adsorption, such as material immobilization.

2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Dhiraj Dutta ◽  
Jyoti Prasad Borah ◽  
Amrit Puzari

Results of investigation on adsorption of Mn2+ from aqueous solution by manganese oxide-coated hollow polymethylmethacrylate microspheres (MHPM) are reported here. This is the first report on Mn-coated hollow polymer as a substitute for widely used materials like green sand or MN-coated sand. Hollow polymethylmethacrylate (HPM) was prepared by using a literature procedure. Manganese oxide (MnO) was coated on the surface of HPM (MHPM) by using the electroless plating technique. The HPM and MHPM were characterized by using optical microscopy (OM), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Optical and scanning micrographs were used to monitor the surface properties of the coated layer which revealed the presence of MnO on the surface of HPM. TGA showed the presence of 4-5% of MnO in MHPM. Adsorption isotherm studies were carried out as a function of pH, initial ion concentration, and contact time, to determine the adsorption efficiency for removal of Mn2+ from contaminated water by the synthesized MHPM. The isotherm results showed that the maximum adsorption capacity of MnO-coated HPM to remove manganese contaminants from water is 8.373 mg/g. The obtained R 2 values of Langmuir isotherm and Freundlich isotherm models were 1 and 0.87, respectively. Therefore, R 2 magnitude confirmed that the Langmuir model is best suited for Mn2+ adsorption by a monolayer of MHPM adsorbent. The material developed shows higher adsorption capacity even at a higher concentration of solute ions, which is not usually observed with similar materials of this kind. Overall findings indicate that MHPM is a very potential lightweight adsorbent for removal of Mn2+ from the aqueous solution because of its low density and high surface area.


2016 ◽  
Vol 4 (12) ◽  
pp. 226-241
Author(s):  
K Veeravelan ◽  
S Arivoli ◽  
V Marimuthu

In the present study, adsorption of copper (II) ions from aqueous solution by Activated Zizyphus Jujuba shell Nano Carbon was investigated under batch mode. The influence of solution pH, sorbent dose, copper concentration, contact time and temperature was studied. The copper adsorption was favored with maximum adsorption at pH 6.5. Sorption equilibrium time was observed in 60 min. The equilibrium adsorption data were correlated with Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Hurkins-Jura, Halsay, Radlich-Peterson, Jovanovic and BET isotherm models. The kinetics of the adsorption process was tested by pseudo-first-order, pseudo-second order, Elovich and Intra-particle diffusion models. It was shown that adsorption of copper could be described by the pseudo-second order kinetic model. Thermodynamic parameters such as Gibbs free energy (ΔG0), the enthalpy (ΔH0) and the entropy change of sorption (ΔS0) have also been evaluated and it has been found that the adsorption process was spontaneous, feasible and endothermic in nature. The results indicated that Activated Zizyphus Jujuba shell Nano Carbon can be used as an effective and low-cost adsorbent to remove copper (II) from aqueous solution.


2014 ◽  
Vol 20 (1) ◽  
pp. 97-107 ◽  
Author(s):  
Mohammad Behnajady ◽  
Shahrzad Yavari ◽  
Nasser Modirshahla

In this work TiO2-P25 nanoparticles with high surface area have been used as adsorbent for the removal of C.I Acid Red 27 (AR27), as an organic contaminant from aqueous solution. Characteristics of phases and crystallite size of TiO2-P25 nanoparticles were achieved from XRD and the surface area and pore size distribution were obtained from BET and BJH techniques. TiO2-P25 nanoparticles with almost 80% anatase and 20% rutile phases, the average crystallite size of 18 nm, have specific surface area of 56.82 m2 g-1. The effect of various parameters like initial AR27 concentration, pH, contact time and adsorbent dosage has been carried out in order to find desired adsorption conditions. The desired pH for adsorption of AR27 onto TiO2-P25 nanoparticles was 3. The equilibrium data were analyzed with various 2-, 3- and 4-parameter isotherm models. Equilibrium data fitted very well by the 4-parameter Fritz-Schluender model. Results of adsorption kinetics study indicated that the pseudo-second order kinetics provided the best fit with correlation coefficients close to unity.


2016 ◽  
Vol 78 (1-2) ◽  
Author(s):  
Nik Ahmad Nizam Nik Malek ◽  
Nurain Mat Sihat ◽  
Mahmud A. S. Khalifa ◽  
Auni Afiqah Kamaru ◽  
Nor Suriani Sani

In the present study, the adsorption of acid orange 7 (AO7) dye from aqueous solution by sugarcane bagasse (SB) and cetylpyridinium bromide (CPBr) modified sugarcane bagasse (SBC) was examined. SBC was prepared by reacting SB with different concentrations (0.1, 1.0 and 4.0 mM) of cationic surfactant, CPBr. The SB and SBC were characterized using Fourier transform infrared (FTIR) spectroscopy. The adsorption experiments were carried out in a batch mode. The effect of initial AO7 concentrations (5-1000 mg/L), initial CPBr concentrations and pH of AO7 solution (2-9) on the adsorption capacity of SB and SBC were investigated. The experimental adsorption data were analyzed using Langmuir and Freundlich isotherm models. The adsorption of AO7 onto SB and SBC followed Freundlich and Langmuir isotherm models, respectively. The maximum uptake of AO7 was obtained by SBC4.0 (SB treated with 4.0 mMCPBr) with the adsorption capacity of 144.928 mg/g. The highest AO7 removal was found to be at pH 2 and 7 for SB and SBC, respectively. As a conclusion, sugarcane bagasse modified with CPBr can become an alternative adsorbent for the removal of anionic compounds in aqueous solution.


2004 ◽  
Vol 40 (1) ◽  
pp. 1-9 ◽  
Author(s):  
E. Deliyanni ◽  
D. Bakoyannakis ◽  
A. Zouboulis ◽  
K. Matis

The application of an innovative, simple and low cost method was tested for the preparation of nanocrystalline iron hydroxides and oxyhydroxides; different iron precursors have been earlier used and combined to different volatile precipitating agents. The examined in the present product, akagan?ite [?-FeO(OH)], had high surface area and definite pore size distribution. The produced materials were examined in detail (i.e. by powder X-ray diffraction, TEM and nitrogen sorption measurement). Main aim of this study was to evaluate the efficiency of the prepared material in the removal of heavy and toxic metal cations, like Cd(II), from aqueous solutions; cadmium constitutes a priority pollutant. Sorption was found to depended on the solution pH and its ionic strength. Typical isotherm models were applied and calculated the values of maximum adsorbent capacity for the metal as well as that of the enthalpy change during the removal process.


Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2563
Author(s):  
Ali Aldalbahi ◽  
Badr M. Thamer ◽  
Mostafizur Rahaman ◽  
Mohamed H. El-Newehy

The high surface area and porosity of self-nitrogen-doped porous carbons (SNPCs) nominates them for potential application in water treatment due to their high efficiency towards the removal of various pollutants. In this study, SNPCs were fabricated from poly(1,5-diaminonaphthalene) (P(1,5-DANPh) by single and simultaneous carbonization at the activation step at different temperatures (600, 700, and 800 °C). The carbonization’s temperature plays a vital role in controlling the nitrogen-doping, surface area, porosity, and morphology of SNPCs. The SNPCs-7 sample prepared at 700 °C showed the highest surface area (1678.8 m2 g−1) with pore volume (0.943 cm3 g−1) with a micro/meso porous structure. The prepared SNPCs were used as an effective adsorbent for removal of crystal violet dye (CV) from contaminated water. SNPCs-7 showed the highest adsorption of 487.53 mg g−1 and the adsorption capacity of the SNPCs samples follows the order SNPCs-7 > SNPCs-8 > SNPCs-6, which is consistent with the results of their surface area and porosity. The adsorption for CV dye followed Freundlich isotherm models and a pseudo second order kinetic model. The negative values of Gipps free energy (ΔG°) and positive value of enthalpy (ΔH°) indicated that the adsorption of CV dye onto the surface of SNPCs was a spontaneous and endothermic process, respectively. Based on the results, the adsorption mechanism of CV dye onto the surface of SNPCs was proposed.


2016 ◽  
Vol 720 ◽  
pp. 31-36 ◽  
Author(s):  
Ryouichi Hikosaka ◽  
Fukue Nagata ◽  
Masahiro Tomita ◽  
Katsuya Kato

Deoxyribonucleic acid (DNA) adsorption onto particles has applications in biosensors, separation methods, and gene delivery. Mesoporous silica (MPS), which exhibits a high surface area and large pore volume, is used in these applications because its pore size is easily controlled and its surface functional groups are easily exchanged. In this study, three types of MPSs with different pore sizes (2.4, 5.6, and 11.8 nm) were functionalized with different aminosilane coupling reagents and the effects of the MPS pore size and surface functional groups on DNA adsorption were evaluated. As the pore size of MPS increased, MPSs with diethylenetriamine (–3NH2) adsorbed higher amounts of DNA, whereas MPSs with hexylenediamine groups (–2HNH2) adsorbed lower amounts of DNA. Moreover, the fitting of DNA adsorption equilibrium data to Langmuir and Freundlich isotherm models was investigated.


2021 ◽  
Vol 2021 ◽  
pp. 1-16
Author(s):  
Hizkeal Tsade Kara ◽  
Sisay Tadesse Anshebo ◽  
Fedlu Kedir Sabir ◽  
Getachew Adam Workineh

The study was focused on the preparation and characterizations of sodium periodate-modified nanocellulose (NaIO4-NC) prepared from Eichhornia crassipes for the removal of cationic methylene blue (MB) dye from wastewater (WW). A chemical method was used for the preparation of NaIO4-NC. The prepared NaIO4-NC adsorbent was characterized by using X-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electron microscope (SEM), energy-dispersive X-ray (EDX), and Brunauer–Emmett–Teller (BET) instruments. Next, it was tested to the adsorption of MB dye from WW using batch experiments. The adsorption process was performed using Langmuir and Freundlich isotherm models with maximum adsorption efficiency (qmax) of 90.91 mg·g−1 and percent color removal of 78.1% at optimum 30 mg·L−1, 60 min., 1 g, and 8 values of initial concentration, contact time, adsorbent dose, and solution pH, respectively. Pseudo-second-order (PSO) kinetic model was well fitted for the adsorption of MB dye through the chemisorption process. The adsorption process was spontaneous and feasible from the thermodynamic study because the Gibbs free energy value was negative. After adsorption, the decreased values for physicochemical parameters of WW were observed in addition to the color removal. From the regeneration study, it is possible to conclude that NaIO4-NC adsorbent was recyclable and reused as MB dye adsorption for 13 successive cycles without significant efficient loss.


2014 ◽  
Vol 884-885 ◽  
pp. 195-199
Author(s):  
Yu Shang ◽  
Jing Hua Zhang ◽  
Yi Ke Li ◽  
Run Ping Han

Pyrolytic-char, a by-product from the slow pyrolysis of pine sawdust, was characterized by FTIR, SEM and XRD, etc. Then it was used as an adsorbent for the removal of cationic dye, neutral red (NR) from solution in batch mode. Adsorption studies were performed at different pH, salt concentration, contact time and dye concentration in the batch mode. Solution pH 6 is favor of adsorption and it is disadvantage of adsorption with common salt existed. Langmuir and Freundlich isotherm models were used to fit the experimental data and Freundlich was better. The adsorption quantity from experiment was up to 272 mg g1at 293 K. PR can effectively adsorb cationic dye from solution.


2009 ◽  
Vol 4 (4) ◽  
Author(s):  
Franciele Regina Furlan ◽  
Laís Graziela de Melo da Silva ◽  
Ayres Ferreira Morgado ◽  
Antônio Augusto Ulson de Souza ◽  
Selene Maria Arruda Guelli Ulson de Souza

The aim of the present study was to investigate the removal of reactive dyes, Black 5 and Orange 16, through a combined coagulation/adsorption process on activated carbon. A coconut-based powdered activated carbon was used as an adsorbent and aluminum chloride was chosen as the coagulant. In order to obtain the best removal conditions for these dyes, the influence of the following parameters were investigated: coagulant dosage, aqueous solution pH, addition of sodium chloride and the application of increased temperature plus sodium chloride. Adsorption results for the reactive dyes were analyzed by Langmuir and Freundlich isotherm models and showed good correlation. The presence of sodium chloride in the mixture resulted in significant adsorption improvement. The influence of increased temperature plus sodium chloride on the dye removal from aqueous solution showed the feasibility of adsorption and its endothermic nature. Through the reactivation experiments it was verified that the adsorbent can be reused three times, consecutively, after the first adsorption with the virgin carbon. For the final evaluation of the effluent, obtained after the coagulation and adsorption process, acute toxicity tests were carried out with Daphnia magna, and the results obtained showed that the final effluent was not toxic. The combined coagulation/adsorption process was found to be an excellent option for the removal of reactive dyes.


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