scholarly journals Coal-Based Activated Carbons for the Removal of Sulphur Dioxide via Adsorption

1997 ◽  
Vol 15 (10) ◽  
pp. 803-814 ◽  
Author(s):  
A.M. Youssef ◽  
M.R. Mostafa ◽  
E.M. Dorgham

Zinc chloride-activated carbons and steam-activated carbons were prepared from Maghara coal. The textural properties were determined from low-temperature nitrogen adsorption. Zinc chloride activation is usually associated with the creation of new micropores while steam activation involves pore widening particularly when the percentage burn-off is high. The adsorption of SO2 on steam-activated carbon is high compared with ZnCl2-activated carbons. Steam activation develops surface basic groups which provide chemisorption sites for SO2. The adsorption of SO2 is enhanced in the presence of O2 and water vapour and involves the formation of sulphuric acid in this case. Sulphur dioxide adsorption is related to the chemistry of the carbon surface rather than to the extent of the surface area of the activated carbon.

1997 ◽  
Vol 15 (1) ◽  
pp. 59-68 ◽  
Author(s):  
Th. El-Nabarawy ◽  
M.R. Mostafa ◽  
A.M. Youssef

Non-activated carbon ‘A’, physically-activated carbons P1–P4, zinc chloride-activated carbons Z1–Z4 and potassium sulphide-activated carbons K1–K4 were prepared from Maghara coal (Sinai, Egypt). The surface areas of these carbons were determined by investigating the adsorption of carbon dioxide at 298 K and of nitrogen at 77 K. The decolourization powers of the carbons were determined from methylene blue adsorption at 308 K. The adsorption of methanol, benzene, n-hexane, n-octane and α-pinene at 308 K was also determined using equilibrium and flow techniques. The removal of ammonia and phenol from water was investigated on some selected samples. The activated carbons showed high capacities towards the removal of organic pollutants from water and from gas streams via adsorption. Their capacity towards a particular pollutant depends on the method of activation and is related to the textural and/or the chemistry of the carbon surface.


1997 ◽  
Vol 15 (6) ◽  
pp. 419-427 ◽  
Author(s):  
M.A. Hourieh ◽  
M.N. Alaya ◽  
A.M. Youssef

A series of activated carbons ‘Z’ was prepared from Aleppo Pistacia Vera shells using different percentages of zinc chloride at 873 K in the absence of air. Another series ‘ZN’ was prepared using the same conditions as for the ‘Z’ series but employing a nitrogen atmosphere to effect carbonization. The textural properties of the two series of samples were determined from the adsorption of carbon dioxide and methylene blue at 298 K. Activated carbons with a high adsorptive capacity for methylene blue were obtained. Activation with zinc chloride proceeded with increasing microporosity via the creation of new micropores. At high percentages of zinc chloride, slight partial pore widening may take place. Carbon dioxide was accessible to the entire pore system and was therefore suitable as a probe for the investigation of the textural properties of the activated carbons studied. A fraction of the porosity was inaccessible to methylene blue molecules and consequently lower surface areas were calculated from the adsorption of this dye molecule.


2014 ◽  
Vol 12 (2) ◽  
pp. 717-726 ◽  
Author(s):  
Zohra Belala ◽  
Meriem Belhachemi ◽  
Mejdi Jeguirim

Abstract Activated carbons were prepared from date pits by physical activation with CO2 and the textural properties were investigated by BET and D-R methods with N2 and CO2 adsorption isotherms. The interaction of the NO2 with activated carbon was examined at ambient temperature and the effect of operating conditions such as temperature and inlet gas compositions was also examined. It was observed that the development of porosity with increasing time of activation favours the adsorption capacity of NO2. The maximum adsorption capacity reached was about 107 mg/g, which is higher than several activated carbon prepared from classical lignocellulosic biomass. However, a slight decrease of NO2 adsorption capacity was observed with increasing temperature. The addition of oxygen into the inlet gas gave rise to an increase in amount adsorbed of NO2.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lilla Fijołek ◽  
Joanna Świetlik ◽  
Marcin Frankowski

AbstractIn water treatment technology, activated carbons are used primarily as sorbents to remove organic impurities, mainly natural organic matter, but also as catalysts in the ozonation process. Commercially available activated carbons are usually contaminated with mineral substances, classified into two main groups: alkali metals (Ca, Na, K, Li, Mg) and multivalent metals (Al, Fe, Ti, Si). The presence of impurities on the carbon surface significantly affects the pHpzc values determined for raw and ozonated carbon as well as their acidity and alkalinity. The scale of the observed changes strongly depends on the pH of the ozonated system, which is related to the diffusion of impurities from the carbon to the solution. In an acidic environment (pH 2.5 in this work), the ozone molecule is relatively stable, yet active carbon causes its decomposition. This is the first report that indirectly indicates that contaminants on the surface of activated carbon (multivalent elements) contribute to the breakdown of ozone towards radicals, while the process of ozone decomposition by purified carbons does not follow the radical path in bulk solution. Carbon impurities also change the distribution of the reaction products formed by organic pollutants ozonation, which additionally confirms the radical process. The study showed that the use of unpurified activated carbon in the ozonation of succinic acid (SA) leads to the formation of a relatively large amount of oxalic acid (OA), which is a product of radical SA degradation. On the other hand, in solutions with purified carbon, the amount of OA generated is negligible.


2015 ◽  
Vol 74 (11) ◽  
Author(s):  
Riry Wirasnita ◽  
Tony Hadibarata ◽  
Abdull Rahim Mohd Yusoff ◽  
Zainab Mat Lazim

An oil palm empty fruit bunch-derived activated carbon has been successfully produced by chemical activation with zinc chloride and without chemical activation. The preparation was conducted in the tube furnace at 500oC for 1 h. The surface structure and active sites of activated carbons were characterized by means of Fourier transform infrared spectrometry and field emission scanning electron microscopy. The proximate analysis including moisture content, ash content, bulk density, pH, and pH at zero charge was conducted to identify the psychochemical properties of the adsorbent. The results showed that the zinc chloride-activated carbon has better characteristics compared to the carbon without chemical activation.  


2021 ◽  
Vol 1162 ◽  
pp. 65-73
Author(s):  
Rakhmawati Farma ◽  
Ona Lestari ◽  
Erman Taer ◽  
Apriwandi ◽  
Minarni ◽  
...  

Heavy metal such as Cu, Fe, and Zn are the most serious contributers to environmental problems. The removal of heavy metal from the environment is the research interest nowdays. The adsorption of Cu, Fe and Zn from wastewater was investigated with various activated carbons as adsorbents. The activated carbons were produced from oil palm leaves by using multi-activation methods. The H3PO4, NaOH, ZnCl2 and KOH were chosen as chemical activating agents. Batch adsorption experiment was used to test the ability of activated carbon to remove Cu, Fe, and Zn from wastewater. The surface characteristics of activated carbon were evaluated using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FTIR), and nitrogen adsorption-desorption isotherms. The Activated carbons were able to purify wastewater with a maximum turbidity level of 2.83 NTU. The AC-H3PO4 activated carbon showed the highest absorbability of Cu metal as 91.540%, while the highest absorbabilities of Zn and Fe metals were indicated by AC-KOH activated carbon of 22.853% and 82.244% absorption respectively. Therefore, these results enable the oil palm leaves to become a high potential for activated carbon as removal the heavy metals.


Energies ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2237
Author(s):  
Sara Stelitano ◽  
Giuseppe Conte ◽  
Alfonso Policicchio ◽  
Alfredo Aloise ◽  
Giovanni Desiderio ◽  
...  

Pinecones, a common biomass waste, has an interesting composition in terms of cellulose and lignine content that makes them excellent precursors in various activated carbon production processes. The synthesized, nanostructured, activated carbon materials show textural properties, a high specific surface area, and a large volume of micropores, which are all features that make them suitable for various applications ranging from the purification of water to energy storage. Amongst them, a very interesting application is hydrogen storage. For this purpose, activated carbon from pinecones were prepared using chemical activation with different KOH/precursor ratios, and their hydrogen adsorption capacity was evaluated at liquid nitrogen temperatures (77 K) at pressures of up to 80 bar using a Sievert’s type volumetric apparatus. Regarding the comprehensive characterization of the samples’ textural properties, the measurement of the surface area was carried out using the Brunauer–Emmett–Teller method, the chemical composition was investigated using wavelength-dispersive spectrometry, and the topography and long-range order was estimated using scanning electron microscopy and X-ray diffraction, respectively. The hydrogen adsorption properties of the activated carbon samples were measured and then fitted using the Langmuir/ Töth isotherm model to estimate the adsorption capacity at higher pressures. The results showed that chemical activation induced the formation of an optimal pore size distribution for hydrogen adsorption centered at about 0.5 nm and the proportion of micropore volume was higher than 50%, which resulted in an adsorption capacity of 5.5 wt% at 77 K and 80 bar; this was an increase of as much as 150% relative to the one predicted by the Chahine rule.


1997 ◽  
Vol 15 (7) ◽  
pp. 531-540 ◽  
Author(s):  
P.J.C. Anstice ◽  
J.F. Alder

An ASC/T (Cu2+, Cr6+, Ag and triethylenediamine impregnated) Whetlerite activated carbon sample was exposed to a flow rate of 1 l/min, 0.746 mg/l SO2 in 80% RH air at 22°C for up to 510 min. Samples were subsequently challenged with 2 mg/l HCN in an identical diluent gas stream. Increasing SO2 exposure resulted in accelerated HCN and (CN)2 bed penetration. The basic shapes of the breakthrough profiles were however essentially unchanged. This observation is in accordance with numerical analysis of these results using Hinshelwood's adsorption model, which suggested that the adsorption rate constant was not significantly affected by SO2 but rather the pollutant exposure resulted in the number of active centres on the carbon surface being reduced and the effective bed depth of the sample being shortened. This loss in active centres was thought most likely to result from the reduction of Cr6+ to Cr3+.


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.


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