scholarly journals ADSORPTION OF METHYLENE BLUE ONTO ACTIVATED CARBON DEVELOPED FROM BAOBAB FRUIT SHELL BY CHEMICAL ACTIVATION: KINETIC EQUILIBRIUM STUDIES

2021 ◽  
Vol 22 (2) ◽  
pp. 31-49
Author(s):  
Radhia Nedjai ◽  
Ma’an Fahmi Rashid Alkhatib ◽  
Md Zahangir Alam ◽  
Nassereldeen Ahmed Kabbashi

This article provides results of the usability of baobab fruit shell to produce activated carbons by chemical activation using ZnCl2, H3PO4, and KOH. This study indicated that activated carbon produced from baobab fruit shell fruit can be used as a promising adsorbent for the removal of methylene blue from aqueous solutions. Significant changes on the material surface following the activation process were observed through SEM and FTIR analyses. Scanning electron micrographs of BFS-ACs showed that porous structures were formed during activation, while the FTIR results indicated that the carbons have abundant functional groups on the surface. KOH activation led an activated carbon with a high methylene blue adsorption of 95.54% and maximum adsorption capacity of 113.63 mg/g, which is directly related to the specific surface area of activated carbons. The adsorption isotherm data were fitted to Langmuir and Freundlich adsorption models. The Langmuir isotherm model showed better fit to the equilibrium data than the Freundlich model. The adsorption process was well described by the pseudo-second-order kinetics. The BFS-ACs is an effective and low-cost adsorbent for the removal of MB from an aqueous solution. ABSTRAK: Kajian ini memberi input tentang kebolehgunaan kulit buah baobab bagi menghasilkan karbon teraktifan melalui aktiviti kimia menggunakan ZnCl2, H3PO4, dan KOH. Karbon aktif daripada kulit buah Baobab ini berpotensi sebagai penyerap bagi menyingkir larutan akueus metilin biru. Perubahan ketara pada permukaan bahan diikuti dengan proses pengaktifan dipantau melalui analisis SEM dan FTIR. Imbasan elektron mikrograf BFS-AC menunjukkan struktur porus terhasil semasa proses pengaktifan. Sementara dapatan FTIR menunjukkan karbon mempunyai banyak kumpulan berfungsi pada permukaan. Pengaktifan KOH menghasilkan karbon aktif menggunakan larutan biru metilin yang tinggi sebanyak 95.54% dan kapasiti maksimum penyerapan 113.63 mg/g, iaitu berkadar langsung dengan tumpuan kawasan permukaan karbon aktif berkaitan. Data isoterma penyerapan dibina pada model penyerapan Langmuir dan Freundlich. Model isoterma Langmuir lebih padan pada data keseimbangan berbanding model Freundlich. Proses penyerapan menunjukkan lebih kinetik order-kedua-pseudo. BFS-AC sangat efektif dan penyerap murah bagi membuang MB daripada larutan akues.

2020 ◽  
Vol 82 (9) ◽  
pp. 1932-1949
Author(s):  
Mondira Bardhan ◽  
Tamanna Mamun Novera ◽  
Mumtahina Tabassum ◽  
Md. Azharul Islam ◽  
Ali H. Jawad ◽  
...  

Abstract In this study, activated carbon (AC) was prepared from agro-waste betel nut husks (BNH) through the chemical activation method. Different characterization techniques described the physicochemical nature of betel nut husks activated carbon (BNH-AC) through Fourier transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET), scanning electron microscopy (SEM), and pH point of zero charge. Later, the produced AC was used for methylene blue (MB) adsorption via numerous batch experimental parameters: initial concentrations of MB dye (25–250 mg/L), contact time (0.5–24 hours) and initial pH (2–12). Dye adsorption isotherms were also assessed at three temperatures where the maximum adsorption capacity (381.6 mg/g) was found at 30 °C. The adsorption equilibrium data were best suited to the non-linear form of the Freundlich isotherm model. Additionally, non-linear pseudo-second-order kinetic model was better fitted with the experimental value as well. Steady motion of solute particles from the boundary layer to the BNH-AC's surface was the possible reaction dynamics concerning MB adsorption. Thermodynamic study revealed that the adsorption process was spontaneous and exothermic in nature. Saline water emerged as an efficient eluent for the desorption of adsorbed dye on AC. Therefore, the BNH-AC is a very promising and cost-effective adsorbent for MB dye treatment and has high adsorption capacity.


Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2951
Author(s):  
Mirosław Kwiatkowski ◽  
Jarosław Serafin ◽  
Andy M. Booth ◽  
Beata Michalkiewicz

This paper presents the results of a computer analysis of the effect of activation process temperature on the development of the microporous structure of activated carbon derived from the leaves of common polypody (Polypodium vulgare) via chemical activation with phosphoric acid (H3PO4) at activation temperatures of 700, 800, and 900 °C. An unconventional approach to porous structure analysis, using the new numerical clustering-based adsorption analysis (LBET) method together with the implemented unique gas state equation, was used in this study. The LBET method is based on unique mathematical models that take into account, in addition to surface heterogeneity, the possibility of molecule clusters branching and the geometric and energy limitations of adsorbate cluster formation. It enabled us to determine a set of parameters comprehensively and reliably describing the porous structure of carbon material on the basis of the determined adsorption isotherm. Porous structure analyses using the LBET method were based on nitrogen (N2), carbon dioxide (CO2), and methane (CH4) adsorption isotherms determined for individual activated carbon. The analyses carried out showed the highest CO2 adsorption capacity for activated carbon obtained was at an activation temperature of 900 °C, a value only slightly higher than that obtained for activated carbon prepared at 700 °C, but the values of geometrical parameters determined for these activated carbons showed significant differences. The results of the analyses obtained with the LBET method were also compared with the results of iodine number analysis and the results obtained with the Brunauer–Emmett–Teller (BET), Dubinin–Radushkevich (DR), and quenched solid density functional theory (QSDFT) methods, demonstrating their complementarity.


2019 ◽  
Vol 6 (9) ◽  
pp. 190523 ◽  
Author(s):  
Lu Luo ◽  
Xi Wu ◽  
Zeliang Li ◽  
Yalan Zhou ◽  
Tingting Chen ◽  
...  

Activated carbon (AC) was successfully prepared from low-cost forestry fir bark (FB) waste using KOH activation method. Morphology and texture properties of ACFB were studied by scanning and high-resolution transmission electron microscopies (SEM and HRTEM), respectively. The resulting fir bark-based activated carbon (ACFB) demonstrated high surface area (1552 m 2 g −1 ) and pore volume (0.84 cm 3 g −1 ), both of which reflect excellent potential adsorption properties of ACFB towards methylene blue (MB). The effect of various factors, such as pH, initial concentration, adsorbent content as well as adsorption duration, was studied individually. Adsorption isotherms of MB were fitted using all three nonlinear models (Freundlich, Langmuir and Tempkin). The best fitting of MB adsorption results was obtained using Freundlich and Temkin. Experimental results showed that kinetics of MB adsorption by our ACFB adsorbent followed pseudo-second-order model. The maximum adsorption capacity obtained was 330 mg g −1 , which indicated that FB is an excellent raw material for low-cost production of AC suitable for cationic dye removal.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
N. Mojoudi ◽  
N. Mirghaffari ◽  
M. Soleimani ◽  
H. Shariatmadari ◽  
C. Belver ◽  
...  

AbstractThe purpose of this study was the preparation, characterization and application of high-performance activated carbons (ACs) derived from oily sludge through chemical activation by KOH. The produced ACs were characterized using iodine number, N2 adsorption-desorption, Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The activated carbon prepared under optimum conditions showed a predominantly microporous structure with a BET surface area of 2263 m2 g−1, a total pore volume of 1.37 cm3 g−1 and a micro pore volume of 1.004 cm3 g−1. The kinetics and equilibrium adsorption data of phenol fitted well to the pseudo second order model (R2 = 0.99) and Freundlich isotherm (R2 = 0.99), respectively. The maximum adsorption capacity based on the Langmuir model (434 mg g−1) with a relatively fast adsorption rate (equilibrium time of 30 min) was achieved under an optimum pH value of 6.0. Thermodynamic parameters were negative and showed that adsorption of phenol onto the activated carbon was feasible, spontaneous and exothermic. Desorption of phenol from the adsorbent using 0.1 M NaOH was about 87.8% in the first adsorption/desorption cycle and did not decrease significantly after three cycles. Overall, the synthesized activated carbon from oily sludge could be a promising adsorbent for the removal of phenol from polluted water.


2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Nurgul Ozbay ◽  
Adife Seyda Yargic

Activated carbons were prepared by carbonization of tomato paste processing industry waste at 500°C followed by chemical activation with KOH, K2CO3, and HCl in N2 atmosphere at low temperature (500°C). The effects of different activating agents and impregnation ratios (25, 50, and 100 wt.%) on the materials’ characteristics were examined. Precursor, carbonized tomato waste (CTW), and activated carbons were characterized by using ultimate and proximate analysis, thermogravimetric analysis (TG/DTG), Fourier transform-infrared (FT-IR) spectroscopy, X-ray fluorescence (XRF) spectroscopy, point of zero charge measurements (pHPZC), particle size analyzer, scanning electron microscopy (SEM), energy dispersive X-ray (EDX) spectroscopy, nitrogen adsorption/desorption isotherms, and X-ray diffraction (XRD) analysis. Activation process improved pore formation and changed activated carbons’ surface characteristics. Activated carbon with the highest surface area (283 m3/g) was prepared by using 50 wt.% KOH as an activator. According to the experimental results, tomato paste waste could be used as an alternative precursor to produce low-cost activated carbon.


2021 ◽  
Vol 1195 (1) ◽  
pp. 012018
Author(s):  
J Y Lai ◽  
L H Ngu

Abstract Activated carbon (AC) is an established adsorbent for organic pollutants reduction, metal removal, and liquid and gas adsorption. Cost analysis corresponds to determining the best approach for AC production depending on activation techniques with different degrees of activation is still minimal in literature. A cost estimation of AC production in laboratory scale using different conventional activation and post-activation surface modification process is performed in this study. This study attempts to develop a cost-friendly selection of activation process from laboratory scale prices. Chemicals and utility costs were acquired from vendor quotes (i.e., Sigma-Aldrich and Fisher Scientific) and Sarawak industrial electricity tariffs based on 100 g production. Oil palm-based ACs produced from five different activation or surface modification methods were compared to ascertain the least expensive production approach in terms of estimated production cost. Of the five methods investigated, method that quoted the least expensive production cost is chemical activation using potassium hydroxide (KOH) with minimum estimated cost of $7.30 whereas the most expensive production cost involves surface modification by polyethyleneimine (PEI) impregnation with cost of $873.00. Therefore, the estimated production cost for KOH activation is the minimum at $0.073 g−1 while the maximum is $8.73 g−1 for PEI impregnation.


2019 ◽  
Vol 15 (3) ◽  
pp. 89
Author(s):  
Doan Nguyen Hoang Anh ◽  
Pham Mai Ly ◽  
Dao Minh Trung

Study on preparation of activated carbons by chemical activation with NaOH using the impregnatio ratio of 3:1 (NaOH:char) from Macadamia nut shell in terms on temperature and time. The research result showed that Methylene Blue (MB) absorption at optimum temperature and time of 300oC and 90 minutes was 205,68 mg and the removal efficiency was 97,59% corresponding to the color reduction from 349,67 Pt-Co to 8,4 Pt-Co. This results showed that activated carbons prepared from Maccadia nut shells and chemical activation with NaOH had the capable of color treatment in textile wastewater.


Materials ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2047 ◽  
Author(s):  
Katarzyna Januszewicz ◽  
Paweł Kazimierski ◽  
Maciej Klein ◽  
Dariusz Kardaś ◽  
Justyna Łuczak

Pyrolysis of straw pellets and wood strips was performed in a fixed bed reactor. The chars, solid products of thermal degradation, were used as potential materials for activated carbon production. Chemical and physical activation processes were used to compare properties of the products. The chemical activation agent KOH was chosen and the physical activation was conducted with steam and carbon dioxide as oxidising gases. The effect of the activation process on the surface area, pore volume, structure and composition of the biochar was examined. The samples with the highest surface area (1349.6 and 1194.4 m2/g for straw and wood activated carbons, respectively) were obtained when the chemical activation with KOH solution was applied. The sample with the highest surface area was used as an adsorbent for model wastewater contamination removal.


2020 ◽  
Vol 38 (5-6) ◽  
pp. 191-204
Author(s):  
AL Paredes-Doig ◽  
A Pinedo-Flores ◽  
J Aylas-Orejón ◽  
D Obregón-Valencia ◽  
MR Sun Kou

Activated carbon was prepared from the seeds of aguaje palm ( Mauritia flexuosa L.f.) by a chemical activation with phosphoric acid. This activated carbon was used for adsorbing metal ions: Pb(II), Cd(II), and Cr(III). To understand the mechanism of adsorption of these heavy metals (Cr, Cd, and Pb), the activated carbon surface was oxidized with nitric acid (1 M) increasing the oxygenated surface groups showing an increasing in their adsorption capacities of these metals. The oxidized activated carbon slightly increased the maximum adsorption capacity to 5–7%. The order of adsorption for unoxidized and oxidized activated carbons was Pb> Cd> Cr. This experimental information was corroborated by molecular modeling program Hyperchem 8 based adsorption mainly on two factors: the electron density and orbitals—highest occupied molecular orbital and lowest unoccupied molecular orbital.Activated carbons were characterized by adsorption/desorption of N2, obtaining an increase of microporous surface area for oxidized activated carbon. An increase of surface acidity and a reduction of isoelectric points were observed in oxidized activated carbon. According to these results, the adsorption of metal ions is favored in contact with an oxidized activated carbon, which has more amount of phenolic and carboxylic functional groups. Similarly, decreasing the isoelectric point indicates that the surface has a higher negative charge. The surface information was corroborated by Hyperchem, which indicates that the surface of the oxidized activated carbon has a higher electron density, indicating a larger amount of electrons on its surface, which means the surface of oxidized activated carbon charges negatively and thereby attracts metal ions.


Molecules ◽  
2020 ◽  
Vol 25 (15) ◽  
pp. 3534
Author(s):  
J. A. Villamil ◽  
E. Diaz ◽  
M. A. de la Rubia ◽  
A. F. Mohedano

In this work, dewatered waste activated sludge (DWAS) was subjected to hydrothermal carbonization to obtain hydrochars that can be used as renewable solid fuels or activated carbon precursors. A central composite rotatable design was used to analyze the effect of temperature (140–220 °C) and reaction time (0.5–4 h) on the physicochemical properties of the products. The hydrochars exhibited increased heating values (up to 22.3 MJ/kg) and their air-activation provided carbons with a low BET area (100 m2/g). By contrast, chemical activation with K2CO3, KOH, FeCl3 and ZnCl2 gave carbons with a well-developed porous network (BET areas of 410–1030 m2/g) and substantial contents in mesopores (0.079–0.271 cm3/g) and micropores (0.136–0.398 cm3/g). The chemically activated carbons had a fairly good potential to adsorb emerging pollutants such as sulfamethoxazole, antipyrine and desipramine from the liquid phase. This was especially the case with KOH-activated hydrochars, which exhibited a maximum adsorption capacity of 412, 198 and 146 mg/g, respectively, for the previous pollutants.


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