Preparation of activated carbons from wet activated sludge by direct chemical activation

2009 ◽  
Vol 59 (12) ◽  
pp. 2387-2394 ◽  
Author(s):  
X. Wang ◽  
N. Zhu ◽  
J. Xu ◽  
B. Yin

An improved method for preparing activated carbons from wet waste activated sludge (WAS) by direct chemical activation was studied in this paper. The effects of processing parameters on iodine adsorption capacity of the product were investigated. Results show that sludge-based activated carbon prepared with KOH had a larger iodine value than those activated with ZnCl2 and KCl. The maximum iodine value was observed at the KOH concentration of 0.50 M. Increasing the impregnation time from 10 to 20 h resulted in a 20% increase in the iodine value. The highest iodine value was obtained at the activation temperature of 600°C and holding time of 1 h. Sludge water content had insignificant effects on the iodine value of products. Raw WAS with a water content of 93.2% can be converted into an activated carbon with a high specific surface area of 737.6 m2 g−1 and iodine value of 864.8 mgg−1 under optimum experimental conditions. Other physical properties such as total pore volume, micropore volume and mean pore diameter of the product were also reported and compared with those of commercial activated carbon.

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.


2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Daouda Kouotou ◽  
Horace Ngomo Manga ◽  
Abdelaziz Baçaoui ◽  
Abdelrani Yaacoubi ◽  
Joseph Ketcha Mbadcam

In this study, activated carbons were prepared from oil palm shells by physicochemical activation. The methodology of experimental design was used to optimize the preparation conditions. The influences of the impregnation ratio (0.6–3.4) and the activation temperature between 601°C and 799°C on the following three responses: activated carbon yield (R/AC-H3PO4), the iodine adsorption (I2/AC-H3PO4), and the methylene blue adsorption (MB/AC-H3PO4) results were investigated using analysis of variance (ANOVA) to identify the significant parameters. Under the experimental conditions investigated, the activation temperature of 770°C and impregnation ratio of 2/1 leading to the R/AC-H3PO4of 52.10%, theI2/AC-H3PO4of 697.86 mg/g, and the MB/AC-H3PO4of 346.25 mg/g were found to be optimum conditions for producing activated carbon with well compromise of desirability. The two factors had both synergetic and antagonistic effects on the three responses studied. The micrographs of activated carbons examined with scanning electron microscopy revealed that the activated carbons were found to be mainly microporous and mesoporous.


2013 ◽  
Vol 773-774 ◽  
pp. 471-477
Author(s):  
Md Mokhlesur Rahman ◽  
Mohamed Awang ◽  
Mohosina Bintey Shajahan ◽  
Tariq Abdul Razak ◽  
Kamaruzzaman Yunus

The optimum condition for preparing a highly efficient activated carbon has been investigated in this work. The effects of different activation temperatures on the pore structure and surface morphology of highly efficient activated carbon (AC) derived from waste palm shell by chemical activation method using phosphoric acid as activating agent were studied. For activation, different activation temperatures in the range of 550 °C-650 °C were carried out. Activated carbon with well developed pore size were produced at activation temperature of 600 °C for 2 hours. At this temperature the Brunauer , Emmett and Teller (BET) surface areas are 1287 m2g-1, the total pore volume for adsorption and desorption are 0.742 cm3 g-1. Scanning Electron Microscope also confirmed the porosity of the highly efficient activated carbon. Finally it was tested in vitro to determine its adsorbing capacity for paraquat as a toxin. For optimum adsorption ability of activated carbon for paraquat, 0.9% NaCl solution is the most suitable solvent. The paraquat preferentially adsorbed onto the activated carbon in NaCl solution. The adsorption ability of the activated carbon (the amount adsorbed) for paraquat observed to be 99.9 mg g-1.


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.


2020 ◽  
Vol 15 (2) ◽  
pp. 79-89
Author(s):  
Sriatun Sriatun ◽  
Shabrina Herawati ◽  
Icha Aisyah

The starting material for activated carbon was biomass from teak woodcutting, which consists of 47.5% cellulose, 14.4% hemicellulose, and 29.9% lignin. The surface area and iodine number of activated carbons are the factors determining the adsorption ability. This study aims to determine the effect of the activator type on activated carbon characters and test the absorption ability for waste cooking oil. The synthesis stages include carbonization, chemical activation, and then physics activation. The activation process consists of two steps. Firstly, the chemical activation via adding H2SO4, and H3PO4 at room temperature for 24 hours, the second, physical activation by heating at various temperatures of 300, 400, and 500 °C for two hours. The characterizations of activated carbon include water content, ash content, iodine number, functional groups, and surface area. Furthermore, the activated carbon was used as an adsorbent for waste cooking oil for 60 minutes at 100 °C with a stirring of 500 rpm. The results were analyzed using UV-Vis spectrophotometry at a maximum wavelength of 403 nm. The iodine numbers of activated carbon ranged 481.1-1211.4 mg/g and 494.8-1204 mg/g for H3PO4 and H2SO4, respectively.Activated carbon with H3PO4 of 15% and an activation temperature of 400 °C has the highest surface area of 445.30 m2/g.  The H2SO4 dan H3PO4 activators can be used to improve the quality of activated carbon in absorbing dyes in waste cooking oil, where the optimum concentration is 10-15% (v/v). The H3PO4 activator tends to produce a higher bleaching percentage than H2SO4. 


BioResources ◽  
2020 ◽  
Vol 16 (1) ◽  
pp. 614-621
Author(s):  
Qingsong Ji ◽  
Haichao Li ◽  
Jingjing Zhang

The object of this study was to prepare activated carbons containing nitrogenous functional groups by a chemical method from nitrogen-containing raw materials. Fish (Ctenopharyngodon idellus) scales were impregnated with phosphoric acid (H3PO4) and activated at varied temperatures. The adsorption ability, structural characteristics, surface chemistry, and morphology of the activated carbons were characterized by methylene blue and iodine values, nitrogen adsorption, the Boehm method, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The total alkaline groups content of the activated carbon produced from fish scales was 0.4330 mmol/g, the total acidic groups was 1.68 mmol/g, the Brunauer–Emmett–Teller (BET) surface area was 501 cm2/g, and the total pore volume was 0.284 cm3/g. The average pore diameter was 1.94 nm under an activation temperature of 550 °C, an activation time of 1 h, and an impregnation ratio of 2. As a result of this study, nitrogenous functional groups that contained acid-base amphoteric adsorbent were produced.


2017 ◽  
Vol 76 (7) ◽  
pp. 1687-1696 ◽  
Author(s):  
Jin Xiao ◽  
Bailie Yu ◽  
Qifan Zhong ◽  
Jie Yuan ◽  
Zhen Yao ◽  
...  

This paper examines a novel method of regenerating saturated activated carbon after adsorption of complex phenolic, polycyclic aromatic hydrocarbons with low energy consumption by using superheated water pretreatment combined with CO2 activation. The effects of the temperature of the superheated water, liquid–solid ratio, soaking time, activation temperature, activation time, and CO2 flow rate of regeneration and adsorption of coal-powdered activated carbon (CPAC) were studied. The results show that the adsorption capacity of iodine values on CPAC recovers to 102.25% of the fresh activated carbon, and the recovery rate is 79.8% under optimal experimental conditions. The adsorption model and adsorption kinetics of methylene blue on regenerated activated carbon (RAC) showed that the adsorption process was in accordance with the Langmuir model and the pseudo-second-order kinetics model. Furthermore, the internal diffusion process was the main controlling step. The surface properties, Brunauer–Emmett–Teller (BET) surface area, and pore size distribution were characterized by Fourier transform infrared spectroscopy (FT-IR) and BET, which show that the RAC possesses more oxygen-containing functional groups with a specific surface area of 763.39 m2 g−1 and a total pore volume of 0.3039 cm3 g−1. Micropores account for 79.8% and mesopores account for 20.2%.


2014 ◽  
Vol 875-877 ◽  
pp. 1585-1589
Author(s):  
Arenst Andreas Arie ◽  
Joong Kee Lee

Activated carbons were prepared from coconut shell by chemical activation method and utilized as electrode materials for electrochemical double layer capacitor (EDLC). A preliminary characteristic of activated carbon from coconut shell includes the Brunnaeur Emmett Teller (BET) analysis and cyclic voltammetry measurements. The BET surface area is not affected by the variation of activation temperature as both of the samples showed BET surface area of about 850-870 m2g-1. The N2 adsorption–desorption isotherms showed that the sample exhibited type I characteristics according to IUPAC classification, which confirms its micro-porosity. Compared with the un-activated carbon samples, the activated ones exhibited the better electrochemical properties with a specific capacitance of 150 F g−1 at a scan rate of 2 mV s−1. The good performance of activated carbon is attributed to the enhancement of surface area due to the KOH pretreatment which can open new pores accessible for the ionic transport


Author(s):  
Mustafa Kaya ◽  
Ömer Şahin ◽  
Cafer Saka

AbstractIn this study, low cost activated carbon was prepared from the pistachio shell by chemical activation with zinc chloride (ZnCl2). The prepared activated carbon was characterized by thermogravimetry (TG) and differential thermal gravimetry (DTG), infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and Brunauer, Emmett and Teller (BET) surface area analyses. Results showed that the activation temperature and impregnation ratio have significant effect on the iodine number of the prepared activated carbon. The optimum conditions for preparing the activated carbon having the highest surface area were found to be an activation temperature of 700 °C, soaking time of 24 h and ZnCl2/ pistachio shell ratio of 50 %. The results showed that the BET surface area, total pore volume, iodine number and methylene blue (MB) number of activated carbon prepared under the optimum conditions were 1108 m2/g, 0.39 cm3/g, 1051 mg/g, 98.48 mg/g, respectively.


2020 ◽  
pp. 174751982097046
Author(s):  
Thu Thuy Luong Thi ◽  
Huu Son Ta ◽  
Khu Le Van

Activated carbons are prepared from coffee husks by chemical activation with ZnCl2 and are characterized by employing Brunauer, Emmett and Teller, scanning electron microscopy, Fourier-transform infrared spectroscopy, and Boehm titrations. The effects of ZnCl2/coffee husks, activation temperature, and activation time are studied, and the results show that the sample ACZ3-600-2 has a high surface area of 1383 m2 g−1, a high pore volume of 1.6482 cm3 g−1, and numerous surface functional groups. The adsorption of reactive red 195 onto the prepared coffee husk activated carbon can be well-described by the pseudo-second-order kinetic model and is found to be controlled by film diffusion followed by intra-particle diffusion. The adsorption isotherm data obtained at 10–40 °C are analyzed and found to follow the Sips model at lower temperatures (10 and 20 °C) and the Redlich–Peterson model at higher temperatures (30 and 40 °C). The obtained thermodynamic parameters (Δ G° < 0, Δ H° = 33.487 kJ mol−1, and Δ S° = 202.30 J K−1 mol−1) suggest that the adsorption of reactive red 195 onto the prepared activated carbon is spontaneous, endothermic, and demonstrates an increasing of randomness at the adsorbate–adsorbent interface. The investigated results show that coffee husk activated carbon is an efficient adsorbent for the removal of reactive red 195 from aqueous solutions.


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