Preparation and TG/DTG, FT-IR, SEM, BET Surface Area, Iodine Number and Methylene Blue Number Analysis of Activated Carbon from Pistachio Shells by Chemical Activation

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.

2011 ◽  
Vol 704-705 ◽  
pp. 517-522 ◽  
Author(s):  
Xiao Juan Jin ◽  
Zhi Ming Yu ◽  
Gao Jiang Yan ◽  
Wu Yu

Activated carbons were prepared through chemical activation of lignin from straw pulping precursor using potassium carbonate as the chemical agent. Effects of activated temperature, K2CO3/lignin ratio and the activated time on the yield, Iodine number of activated carbon were investigated. Experimental results indicated that the optimum conditions were as follow: activated temperature 800°C, K3CO3(40% concentration) /lignin ratio 5: l, activated time 50min. These conditions allowed us to obtain a BET surface area of 1104 m2/g, including the external or non-microporous surface of 417 m2/g,Amount of methylene blue adsorption, Iodine number and the yield of activated carbon prepared under optimum conditions were 10.6mL/0.lg,1310 mg/g and 19.75%, respectively.


2010 ◽  
Vol 44-47 ◽  
pp. 2562-2568
Author(s):  
Wu Yu ◽  
Ming Yu Zhi ◽  
Xiao Juan Jin

Activated carbons were prepared from waste particle board (WPB) by K2CO3 activation. The effects of different parameters, such as chemical/WPB ratio, activation time and activation temperature on yield, the methylene blue adsorption, Iodine number of activated carbon were investigated. The optimum conditions were determined by the method of factor analysis and the orthogonal design as follows: activation temperature 900°C, K2CO3 (50% concentration)/ WPB 4.0, activation time 60 min. Amount of methylene blue adsorption, Iodine number, phenol adsorption, BET surface area and the yield of activated carbon prepared under optimum conditions were 82.5mg/g, 1234mg/g, 185mg/g, 1026m2/g and 30.4%, respectively.


2014 ◽  
Vol 881-883 ◽  
pp. 579-583 ◽  
Author(s):  
Ling Zhi Chen ◽  
Dong Xu Miao ◽  
Xiao Jie Feng ◽  
Jian Zhong Xu

Activated carbons (AC) were produced by chemical activation with potassium hydroxide (KOH) at 800°C from chars that were carbonized from reedy grass leaves at 450°C in N2atmosphere. The effects of the weight ratio of KOH/char ( impregnation ratio), activation temperature and duration time were examined. Adsorption capacity was demonstrated with iodine number. BET surface area, pore volume and pore size of activated carbons were characterized by N2adsorption isotherms. The maximum surface area and iodine number of the AC was 1100 m2/g and 1080 mg/g produced at 800°C for2h and impregnation ratio is 4:1.The characteristics of activated carbons were determined by Infrared spectroscopy (FT-IR) and X-ray diffraction (XRD). Thermal gravimetry (TG/DTA) analysis of raw material was carried out.


2021 ◽  
Vol 11 (5) ◽  
pp. 12662-12679

In this study, Chemical activation was used to prepare a low-cost activated carbon (AC) from agricultural waste material: Cucumis melo. It was used as a green biosorbent for the removal of cationic and anionic dyes from aqueous solutions (Methylene blue (MB) and Acid orange 7 (AO7)).A full factorial 24 experimental design was used to optimize the preparation conditions. The factors and levels included are activation temperature (300 and 500ºC), activation time (1 and 3 h), H3PO4 concentration (1.5 and 2.5 mol/L), and contact time (60 and 90 min). The surface area of the activated carbons and high removal efficiency of MB and AO7 was chosen as a measure of the optimization. The activated carbon prepared at 500 °C, for 3 hours with an H3PO4 concentration of 2.5 mol/L and a contact time of 90 min, have the largest specific surface area (475 m2/g) and the percentage of discoloration of methylene blue (99.4%). Furthermore, the greater value of AO7 removal (94.20%) was obtained at 3h - activation time, 500°C - activation temperature, 1.5 mol/L - H3PO4 concentration with a 90 min contact time.


2018 ◽  
Vol 6 (1) ◽  
pp. 46
Author(s):  
Nkwaju Yanou Rachel ◽  
Baçaoui Abdelaziz ◽  
Ndi Julius Nsami ◽  
Kouotou Daouda ◽  
Yaacoubi Abdelrani ◽  
...  

AgNO3- activated carbon composite based palm kernel shell was prepared by hydrothermal carbonization. The concentration of AgNO3, activation temperature and impregnation time were investigated on five responses (iodine number, methylene blue number, BET surface area, micropore volume and total pore volume). The most influential parameters of the preparation process were optimized using the Doehlert optimal design. From the ANOVA, the following optimal conditions of preparation were retained: 0.068 mol/L, 210°C and 3.7 h for AgNO3 concentration, activation temperature and impregnation time respectively. The activated carbon (AC) and the composite (AC-AgNO3) were characterized using Fourier Transform infrared spectroscopy, X-Ray diffraction, Scanning Electron Microscopy coupled to Energy Dispersive X-ray spectroscopy and measurements of the surface area. The XRD pattern and SEM-EDX clearly confirmed the presence of silver in the composite. The experimental parameters of AC- AgNO3 composite were as followed: 708.44 mg/g; 293.09 mg/g; 713.0 m2/g; 0.49 cm3/g and 0.76 cm3/g, for iodine number, methylene blue number, BET surface area, micropore volume and total pore volume of AC- AgNO3 respectively. The antibacterial test carried on Escherichia Coli showed that AC-AgNO3 composite has a high-improved antibacterial property of 99.99% fixation with a dosage of 1500 ppm for 5 hours of contact time.


TAPPI Journal ◽  
2018 ◽  
Vol 17 (02) ◽  
pp. 63-69 ◽  
Author(s):  
Mamon Sarkar ◽  
Chao Tian ◽  
M. Sarwar Jahan

Activated carbon was prepared by phosphoric acid (H3PO4) activation of potassium hydroxide (KOH) pulping spent liquor lignin from rice straw and compared with KOH hydroxide activation. The process parameters, such as impregnation ratio, activation temperature, and activation time were varied and their effects on the yield of activated carbon and iodine number were studied. The activated carbon prepared by H3PO4 at 800°C for 60 min at an impregnation ratio of 2.5 reached a Brunauer-Emmett-Teller (BET) surface area of 1063 m2/g, including pore diameter of 14.4 nm, iodine number of 525 mg/g, and yield of 49.2%. Yield and BET surface area in KOH activation was much lower than that of H3PO4.


2010 ◽  
Vol 129-131 ◽  
pp. 1151-1155 ◽  
Author(s):  
Xiao Juan Jin ◽  
Zhi Ming Yu ◽  
Zhe Ren ◽  
Xin Liu

Activated carbons were prepared through chemical activation of waste particle board (WPB) precursor using potassium hydroxide as the chemical agent. The effects of different parameters, such as chemical/WPB ratio, activation time and activation temperature on yield and the methylene blue adsorption capacity of activated carbon were investigated. Experimental results indicated that the optimum conditions were as follow: activation temperature 850°C, KOH(50% concentration)/ WPB 4.0, activation time 50 min. Amount of methylene blue adsorption, Iodine number and the yield of activated carbon prepared under optimum conditions were 15.0 mL/0.lg, 1213mg/g and 36.9%, respectively. Therefore, great potential exists for developing activated carbon products from waste wood, which will have the positive effects of reducing our landfill problem and gain attractive products.


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. 


2016 ◽  
Vol 22 (2) ◽  
pp. 155-165 ◽  
Author(s):  
Safiye Bağcı ◽  
Ayhan Ceyhan

The adsorption of methylene blue (MB) from synthetic aqueous solutions in batch experiments using Lupinus Albus-activated carbon (LAAC) by chemical activation with zinc chloride was investigated. Prior to adsorption experiments, surface/physical properties of LAAC were determined using Scanning Electron Microscopy, Fourier transform infrared Spectroscopy and nitrogen adsorption isotherm. In the adsorption experiments, effects of adsorption time, solution pH, MB concentration and amount of LAAC were investigated. The isotherm and kinetic parameters were used to describe the experimental data. The BET surface area was 1254 m2/g while its total pore volume was found to be 0.484 cm3/g. Maximum adsorption capacity occurred at solution pH value 10 and was recorded as 109.89 mg/g. Adsorption data were modeled using Langmuir, Freundlich and Temkin adsorption isotherms. Langmuir isotherm and pseudo-second-order models fit to the process and reaction kinetics correspondingly.


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%.


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