Application of Chlorine Dioxide for Restoring the Adsorption Capacity of Activated Carbon Wasted under Industrial Conditions

2020 ◽  
Vol 42 (3) ◽  
pp. 171-177
Author(s):  
N. A. Klymenko ◽  
L. A. Savchyna ◽  
L. K. Patiuk ◽  
S. V. Grechanik
2020 ◽  
Vol 5 (3) ◽  
pp. 221
Author(s):  
Muhammad Azam ◽  
Muhammad Anas ◽  
Erniwati Erniwati

This study aims to determine the effect of variation of activation temperature of activated carbon from sugar palm bunches of chemically activatied with the activation agent of potassium silicate (K2SiO3) on the adsorption capacity of iodine and methylene blue. Activated carbon from bunches of sugar palmacquired in four steps: preparationsteps, carbonizationstepsusing the pyrolysis reactor with temperature of 300 oC - 400 oC for 8 hours and chemical activation using of potassium silicate (K2SiO3) activator in weight ratio of 2: 1 and physical activation using the electric furnace for 30 minutes with temperature variation of600 oC, 650 oC, 700 oC, 750 oC and 800 oC. The iodine and methyleneblue adsorption testedby Titrimetric method and Spectrophotometry methodrespectively. The results of the adsorption of iodine and methylene blue activated carbon from sugar palm bunches increased from 240.55 mg/g and 63.14 mg/g at a temperature of 600 oC to achieve the highest adsorption capacity of 325.80 mg/g and 73.59 mg/g at temperature of 700 oC and decreased by 257.54 mg/g and 52.03 mg/g at a temperature of 800 oCrespectively.However, it does not meet to Indonesia standard (Standard Nasional Indonesia/SNI), which is 750 mg/g and 120 mg/g respectively.


Water ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 598
Author(s):  
David Ribes ◽  
Emilia Morallón ◽  
Diego Cazorla-Amorós ◽  
Francisco Osorio ◽  
María J. García-Ruiz

The adsorption and electroadsorption of bromide from natural water has been studied in a filter-press electrochemical cell using a commercial granular activated carbon as the adsorbent. During electroadsorption experiments, different voltages were applied (2 V, 3 V and 4 V) under anodic conditions. The presence of the electric field improves the adsorption capacity of the activated carbon. The decrease in bromide concentration observed at high potentials (3 V or 4 V) may be due to the electrochemical transformation of bromide to Br2. The anodic treatment produces a higher decrease in the concentration of bromide in the case of cathodic electroadsorption. Moreover, in this anodic electroadsorption, if the system is again put under open circuit conditions, no desorption of the bromide is produced. In the case of anodic treatment in the following adsorption process after 24 h of treatment at 3 V, a new decrease in the bromide concentration is observed as a consequence of the decrease in bromide concentration after the electrochemical stage. It can be concluded that the electroadsorption process is effective against the elimination of bromide and total bromine in water, with a content of 345 and 470 µg L−1, respectively, reaching elimination values of 46% in a single-stage electroadsorption process in bromide and total bromine. The application of the electric field to the activated carbon with a positive polarization (anodic electroadsorption) increases the adsorption capacity of the activated carbon significantly, achieving a reduction of up to 220 µg L−1 after 1 h of contact with water. The two stage process in which a previous electrochemical oxidation is incorporated before the electroadsorption stage significantly increased the efficiency from 46% in a single electroadsorption step at 3 V, to 59% in two stages.


2021 ◽  
Vol 15 (2) ◽  
pp. 131-144
Author(s):  
Chunjiang Jin ◽  
Huimin Chen ◽  
Luyuan Wang ◽  
Xingxing Cheng ◽  
Donghai An ◽  
...  

In this study, aspen wood sawdust was used as the raw material, and Fe(NO3)3 and CO2 were used as activators. Activated carbon powder (ACP) was produced by the one-step physicochemical activation method in an open vacuum tube furnace. The effects of different mass ratios of Fe(NO3)3 and aspen wood sawdust on the pore structure of ACP were examined under single-variable experimental conditions. The mass ratio was 0–0.4. The detailed characteristics of ACP were examined by nitrogen adsorption, scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The adsorption capacity of ACP was established by simulating volatile organic compounds (VOCs) using ethyl acetate. The results showed that ACP has a good nanostructure with a large pore volume, specific surface area, and surface functional groups. The pore volume and specific surface area of Fe-AC-0.3 were 0.26 cm3/g and 455.36 m2/g, respectively. The activator played an important role in the formation of the pore structure and morphology of ACP. When the mass ratio was 0–0.3, the porosity increased linearly, but when it was higher than 0.3, the porosity decreased. For example, the pore volume and specific surface area of Fe-AC-0.4 reached 0.24 cm3/g and 430.87 m2/g, respectively. ACP presented good VOC adsorption performance. The Fe-AC-0.3 sample, which contained the most micropore structures, presented the best adsorption capacity for ethyl acetate at 712.58 mg/g. Under the action of the specific reaction products nitrogen dioxide (NO2) and oxygen, the surface of modified ACP samples showed different rich C/O/N surface functional groups, including C-H, C=C, C=O, C-O-C, and C-N.


Author(s):  
Joanna Srenscek-Nazzal ◽  
Urszula Narkiewicz ◽  
Antoni W. Morawski ◽  
Rafal J. Wróbel ◽  
Beata Michalkiewicz

1997 ◽  
Vol 35 (7) ◽  
pp. 279-285 ◽  
Author(s):  
P. C. Chiang ◽  
E. E. Chang ◽  
J. S. Wu

In this investigation, nine typical compounds, i.e., phenol, 2-aminophenol, aniline, 2-chlorophenol, chlorobenzene, β-naphthol, naphthalene, α-naphthylamine and α-chloronaphthalene were introduced to evaluate the effects of the molecular structure and physicochemical properties of these selected adsorbates on the adsorption capacity and desorption efficiency of the activated carbon. Both the thermal and chemical regeneration methods were employed to compare the regeneration efficiencies among these adsorbates and adsorbent.


Author(s):  
Nawwarah Mokti ◽  
Azry Borhan ◽  
Siti Nur Azella Zaine ◽  
Hayyiratul Fatimah Mohd Zaid

The use of an activating agent in chemical activation of activated carbon (AC) production is very important as it will help to open the pore structure of AC as adsorbents and could enhance its performance for adsorption capacity. In this study, a pyridinium-based ionic liquid (IL), 1-butylpyridinium bis(trifluoromethylsulfonyl) imide, [C4Py][Tf2N] has been synthesized by using anion exchange reaction and was characterized using few analyses such as 1H-NMR, 13C-NMR and FTIR. Low-cost AC was synthesized by chemical activation process in which rubber seed shell (RSS) and ionic liquid [C4Py][Tf2N] were employed as the precursor and activating agent, respectively. AC has been prepared with different IL concentration (1% and 10%) at 500°C and 800°C for 2 hours. Sample AC2 shows the highest SBET and VT which are 392.8927 m2/g and 0.2059 cm3/g respectively. The surface morphology of synthesized AC can be clearly seen through FESEM analysis. A high concentration of IL in sample AC10 contributed to blockage of pores by the IL. On the other hand, the performance of synthesized AC for CO2 adsorption capacity also studied by using static volumetric technique at 1 bar and 25°C. Sample AC2 contributed the highest CO2 uptakes which is 50.783 cm3/g. This current work shows that the use of low concentration IL as an activating agent has the potential to produce porous AC, which offers low-cost, green technology as well as promising application towards CO2 capture.


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