Assessment of chemically modified sugarcane bagasse for lead adsorption from aqueous medium

2010 ◽  
Vol 62 (2) ◽  
pp. 457-465 ◽  
Author(s):  
V. C. G. Dos Santos ◽  
C. R. T. Tarley ◽  
J. Caetano ◽  
D. C. Dragunski

This study evaluated the adsorption capacity of chemically modified sugarcane bagasse with citric acid (B-CA), sodium hydroxide (B-S) and citric acid and sodium hydroxide (B-CAS) for Pb2 +  ion adsorption in aqueous medium. Infrared spectroscopy (FT-IR) was used to characterise the materials, where the chemical modification was confirmed by the presence of carboxylate groups created at 1,730 cm−1 peak. All assays related to Pb2 +  ion adsorption onto adsorbent, i.e. equilibrium time between Pb2 +  ions and adsorbate (24 h), as well as Pb2 +  ion concentration, were performed in batch system. The initial and final Pb2 +  ion concentration after shaking time was determined by Flame Atomic Absorption Spectrometry (FAAS). Isotherm adsorptions were applied to Langmuir and Freundlich linear models and maximum adsorption capacity (MAC) of materials towards Pb2 +  ions was calculated in function of modifications. A significant improvement regarding Pb2 +  ion adsorption after the bagasse treatment with citric acid, in which MAC was 52.63 mg g−1, was observed. The adsorptions followed the behaviour described by the Langmuir linear model and its kinetics follow the behaviour described by the pseudo-second-order equation.

2017 ◽  
Vol 8 (3) ◽  
pp. 200-205
Author(s):  
Thi Thuy Pham ◽  
Thanh Hoa Dinh ◽  
Manh Khai Nguyen ◽  
Bart Van der Bruggen

This study investigated the chemical modification method by citric acid and its enhancement effect on the adsorption capacity of sugarcane bagasse (SB) for copper removal from aqueous solution. Characterization studies were performed by using Fourier transform infra red (FTIR), which showed the introduction of carboxylic group in the structure the modified sugarcane bagasse (MSB). Batch study revealed the influence of pH, time, initial concentration of metal ion on adsorption capacity. The data showed an extremely good fit to Langmuir isotherm model from which the maximum adsorption capacity estimated reached 28.17 mg/g at optimum pH 5.5. Fixed bed column study using the adsorbent MSB confirmed that the breakthrough curves of the adsorption processes were de- pendent on bed height, initial concentration and flow rate. Linear regression analysis of the data demonstrated that Yoon-Nelson kinetic models were appropriate to explain the breakthrough curves. Nghiên cứu đã thực hiện biến tính hóa học vật liệu bã mía bằng acid citric và đánh giá khả năng hấp phụ ion Cu(II) trong nước của bã mía (SB) trước và sau biến tính axit citric. Khảo sát cấu trúc vật liệu thông qua phổ hồng ngoại FTIR cho thấy các nhóm chức carboxylic có khả năng hấp phụ kim loại xuất hiện trong vật liệu biến tính. Thí nghiệm mẻ đánh giá sự ảnh hưởng của pH, thời gian và nồng độ của vật liệu tự nhiên và biến tính đến khả năng hấp phụ ion Cu(II). Kết quả của thí nghiệm mẻ phù hợp với mô hình Langmuir với khả năng hấp phụ cực đại đạt 28,17 mg/g tại nồng độ pH tối ưu là 5,5. Kết quả thí nghiệm trên mô hình cột cho thấy đường cong thoát của quá trình hấp phụ của vật liệu biến tính và chưa biến tính phụ thuộc và chiều cao lớp vật liệu, nồng độ ion Cu(II) ban đầu và vận tốc dòng chảy qua cột. Các dữ liệu thu nhận được từ thực nghiệm phù hợp với mô hình động học Yoon-Nelson.


2020 ◽  
Vol 2 (6) ◽  
pp. 175-181
Author(s):  
Ho Thi Yeu Ly ◽  
Hoang Thi Khanh Dieu ◽  
Trinh Minh Tan Sang ◽  
Le Nguyen Minh Nha

The use of adsorbent prepared from sugarcane bagasse, an agro waste from sugar industries has been studied as an alternative substitute for activated carbon for the removal of dyes from aqueous solution. Adsorbents prepared from sugarcane bagasse modified with citric acid was used as a low-cost biosorbent for removal of dyes from the aqueous solution. Adsorption parameters such as initial pH values, dyes concentrations, adsorbent dosages and contact times were investigated by the batch experiments. The Freundlich and Langmuir adsorption isotherm models were used to evaluate the experimental data. The results showed that the adsorption process of dyes onto the modified sugarcane bagasse leaned towards Langmuir model for MSB and Freundlich for SB. Maximum adsorption capacity of MSB was found to be 8.40 mg/g at pH 9. The results showed that the modified sugarcane bagasse with citric acid could be a potential low-priced adsorbent for removal of the color from the aqueous solution.  


Author(s):  
Anwar Ameen Hezam Saeed ◽  
Noorfidza Yub Harun ◽  
Suriati Sufian ◽  
Muhammad Roil Bilad ◽  
Zaki Yamani Zakaria ◽  
...  

Development of strategies for removing heavy metals from aquatic environments is in high demand. Cadmium is one of the most dangerous metals in the environment, even under extremely low quantities. In this study, kenaf and magnetic biochar composite were prepared for the adsorption of Cd2+. The synthesized biochar was characterized using (a vibrating-sample magnetometer VSM), Scanning electron microscopy (SEM), X-ray powder diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The adsorption batch study was carried out to investigate the influence of pH, kinetics, isotherm, and thermodynamics on Cd2+ adsorption. The characterization results demonstrated that the biochar contained iron particles that help in improving the textural properties (i.e., surface area and pore volume), increasing the number of oxygen-containing groups, and forming inner-sphere complexes with oxygen-containing groups. The adsorption study results show that optimum adsorption was achieved under pH 5–6. An increase in initial ion concentration and solution temperature resulted in increased adsorption capacity. Surface modification of biochar using iron oxide for imposing magnetic property allowed for easy separation by external magnet and regeneration. The magnetic biochar composite also showed a higher affinity to Cd2+ than the pristine biochar. The adsorption data fit well with the pseudo-second-order and the Langmuir isotherm, with the maximum adsorption capacity of 47.90 mg/g.


Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1068
Author(s):  
Xinyue Zhang ◽  
Yani Guo ◽  
Wenjun Li ◽  
Jinyuan Zhang ◽  
Hailiang Wu ◽  
...  

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.


2020 ◽  
Vol 11 (4) ◽  
pp. 11891-11904

In the present study, batch mode adsorption was carried out to investigate the adsorption capacity of dried bael flowers (Aegle marmelos) for the adsorptive removal of Cu(II) ions from aqueous solutions by varying agitation time, initial metal concentration, the dose of adsorbent, temperature, and initial pH of the Cu(II) ion solution. The percentage removal of 98.7% was observed at 50 ppm initial metal ion concentration, 0.5 g/100.00 cm3 adsorbent dosage, within the contact time of 120 minutes at 30 ºC in the pH range of 4 – 7. The sorption processes of Cu(II) ions was best described by pseudo-second-order kinetics. Langmuir isotherm had a good fit with the experimental data with 0.97 of correlation coefficient (R2), and the maximum adsorption capacity obtained was 23.14 mg g-1 at 30 ºC. The results obtained from sorption thermodynamic studies suggested that the adsorption process is exothermic and spontaneous. SEM analysis showed tubular voids on the adsorbent. FTIR studies indicated the presence of functional groups like hydroxyl, –C-O, –C=O, and amide groups in the adsorbent, which can probably involve in metal ion adsorption. Therefore, dried bael flowers can be considered an effective low-cost adsorbent for treating Cu(II) ions.


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.


2012 ◽  
Vol 65 (8) ◽  
pp. 1341-1349 ◽  
Author(s):  
Shokooh Sadat Khaloo ◽  
Amir Hossein Matin ◽  
Sahar Sharifi ◽  
Masoumeh Fadaeinia ◽  
Narges Kazempour ◽  
...  

The application of almond shell as a low cost natural adsorbent to remove Hg2+ from aqueous solution was investigated. Batch experiments were carried out to evaluate the adsorption capacity of the material. The chemical and physical parameters such as pH, sorbent amount, initial ion concentration, and contact time were optimized for the maximum uptake of mercury onto the solid surface. Adsorption isotherms were expressed by Langmuir and Freundlich adsorption models, and the experimental data were found to fit the Langmuir model rather than the Freundlich. The maximum adsorption capacity obtained from the Langmuir isotherm was 135.13 mg/g. A kinetic study was carried out with pseudo-first-order and pseudo-second-order reaction equations and it was found that the Hg2+ uptake process followed the pseudo-second-order rate expression. The thermodynamic values, ΔG0, ΔH0 and ΔS0, indicated that adsorption was an endothermic and spontaneous process. The potential of this material for mercury elimination was demonstrated by efficient Hg2+ removal from a synthetic effluent.


Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6885
Author(s):  
Ashraf Ali ◽  
Sarah Alharthi ◽  
Bashir Ahmad ◽  
Alia Naz ◽  
Idrees Khan ◽  
...  

The adsorptive removal of lead (II) from aqueous medium was carried out by chemically modified silica monolith particles. Porous silica monolith particles were prepared by the sol-gel method and their surface modification was carried out using trimethoxy silyl propyl urea (TSPU) to prepare inorganic–organic hybrid adsorbent. The resultant adsorbent was evaluated for the removal of lead (Pb) from aqueous medium. The effect of pH, adsorbent dose, metal ion concentration and adsorption time was determined. It was found that the optimum conditions for adsorption of lead (Pb) were pH 5, adsorbent dose of 0.4 g/L, Pb(II) ions concentration of 500 mg/L and adsorption time of 1 h. The adsorbent chemically modified SM was characterized by scanning electron microscopy (SEM), BET/BJH and thermo gravimetric analysis (TGA). The percent adsorption of Pb(II) onto chemically modified silica monolith particles was 98%. An isotherm study showed that the adsorption data of Pb(II) onto chemically modified SM was fully fitted with the Freundlich and Langmuir isotherm models. It was found from kinetic study that the adsorption of Pb(II) followed a pseudo second-order model. Moreover, thermodynamic study suggests that the adsorption of Pb(II) is spontaneous and exothermic. The adsorption capacity of chemically modified SM for Pb(II) ions was 792 mg/g which is quite high as compared to the traditional adsorbents. The adsorbent chemically modified SM was regenerated, used again three times for the adsorption of Pb(II) ions and it was found that the adsorption capacity of the regenerated adsorbent was only dropped by 7%. Due to high adsorption capacity chemically modified silica monolith particles could be used as an effective adsorbent for the removal of heavy metals from wastewater.


2020 ◽  
Vol 1 (1) ◽  
pp. 37-44
Author(s):  
Krishna Bahadur Dawadi ◽  
Mahesh Bhattarai ◽  
Puspa Lal Homagai

Adsorptive removal of methyl red (MR) from aqueous solution onto chemically modified Charred Sal (Shorea robusta) Saw-Dust (CSSD) and Xanthated Sal Saw-Dust (XSSD) has been investigated. The surface modification is characterized by Fourier transformed infra-red (FTIR) spectroscopy, scanning electron microscopy (SEM) and elemental Analysis. Different parameters are studied such as contact time, optimum pH, and initial ion concentration. Maximum dye removal is observed at pH 4 for charred and xanthated Sal saw dust. The dye can be quantitatively removed onto the surface of these adsorbent. At a contact time of 3-4 hours maximum adsorption capacity (qmax) for CSSD and XSSD are found to be 70 mg/g and 130 mg/g respectively. Adsorption kinetic data are best fitted onto pseudo second order. The obtained result indicated an excellent alternative for the treatment of dye contaminated waste water using such chemically modified Sal saw dust at low cost with better efficiency.


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