scholarly journals Effect of Different Treatment on the Adsorption of p-Cresol by Activated Carbon

2017 ◽  
Vol 5 (1) ◽  
pp. 55 ◽  
Author(s):  
Sirous Nouri
Keyword(s):  
Activated Carbon ◽  
Adsorption Capacity ◽  
Activated Carbons ◽  
Molecular Form ◽  
Carbon Surface ◽  
Ionic Form ◽  
Freundlich Model ◽  
London Dispersion ◽  
Carbon Change ◽  
London Dispersion Forces

<p>Adsorption of p-Cresol by three activated carbons (one untreated and two treated) was carried out at 301 K and at controlled pH conditions. By treating the activated carbon the PZC and adsorption capacity (Q<sub>max</sub>) of carbon change. The adsorption capacity of each carbon, by using the homogenous Langmuir-Freundlich model, was found to comparing the effect of different treatment. At pH lower than pK<sub>a</sub> of p-cresol (molecular form), it was observed that the electron density of aromatic ring and also those of the carbon surface, are the main forces involved in the adsorption process, by affecting the extent of London dispersion forces. Treating by H<sub>2</sub> increase the PZC and treating by H<sub>2</sub>SO<sub>4</sub> decrease this factor. At higher pH (in ionic form), it was found that the electrostatic forces played a significant role on the extent of adsorption. In this condition the adsorption of the solute dependent on the concentration of anionic form of the solute. The effect of pH must be considered from its combined effects on the carbon surface and on the solute molecules. It was found that the uptake of the molecular form of the aromatic solute was dependent on the PZC of the carbon.</p>

SURFACE MODIFICATIONS OF ACTIVATED CARBON AND ITS IMPACT ON APPLICATION

2019 ◽  
Vol 26 (01) ◽  
pp. 1830006 ◽  
Author(s):  
MATHEUS PEGO ◽  
JANAÍNA CARVALHO ◽  
DAVID GUEDES
Keyword(s):  
Surface Modification ◽  
Activated Carbon ◽  
Surface Chemistry ◽  
Surface Structure ◽  
Adsorption Capacity ◽  
Activated Carbons ◽  
Surface Modifications ◽  
Hazardous Substances ◽  
Carbon Surface ◽  
Corona Treatment

The main and new surface modification methods of activated carbon (AC) and their influence on application (adsorption capacity) were reviewed. Adsorption capacity is an important issue, contributing to hazardous substances environment management. According to literature, it is true that surface chemistry strongly affects adsorption capacity. Surface chemistry can be modified by several methods that lead to different activated carbon properties. Furthermore, adsorbate properties, and their relationships with surface structure, can impact adsorption properties. Surface modifications can be conducted by adding some atoms to the surface structure, making the surface more acidic or basic. Introduction of oxygen and ammonia atoms (chemical modification) are the main processes to make the surface more acidic and basic, respectively, although may bring chemical wastes to environment. Surface modification is done by chemical and physical modifications that lead activated carbons to present different properties. The main and new methods of chemical and physical modifications are compared and presented in this paper. Some new physical methods, like corona treatment, plasma discharge and microwave radiation, can be applied to cause surface modifications. Corona treatment can be a practical and new way to cause surface modification on an activated carbon surface.

scholarly journals Effect of Treatment on the Adsorption Capacity of Activated Carbon

2002 ◽  
Vol 20 (9) ◽  
pp. 917-925 ◽  
Author(s):  
Sirous Nouri
Keyword(s):  
Adsorption Capacity ◽  
Activated Carbons ◽  
Ph Value ◽  
Carbon Surface ◽  
Point Of Zero Charge ◽  
Molecular Forms ◽  
Model Parameters ◽  
Ionic Form ◽  
Solution Ph ◽  
Adsorption Affinity

The adsorption of p-cresol by three activated carbons, one untreated S.E.I. and the other two treated S.E.I., was carried out under controlled conditions. Such treatment led to a change in the point of zero charge (PZC) and the adsorption capacity (Qmax) of the carbon concerned. The adsorption capacity and affinity (K1) of each carbon was determined using the Langmuir homogeneous and binary models to compare the effects of different treatments on these and relative parameters. The variation of the model parameters with the solution pH was also studied. The fitted parameters obtained from both models showed the pH value had the most significant effect on the adsorption capacity (Qmax) and the adsorption affinity (K1) of a given carbon, with both quantities showing a decrease with increasing pH. It was found that the uptake of the molecular forms of the aromatic solute was dependent on the PZC of the carbons. Treatment with H2 increased the PZC whilst treatment with H2SO4 led to a decrease in this factor. At higher pH (when the solute was in an ionic form), it was found that electrostatic forces played a significant role on the extent of adsorption. Under these conditions, the adsorption of the solute depended on the concentration of its anionic form. It was shown that the effect of pH must be considered from the viewpoint of its combined effect on the carbon surface and on the solute molecules.

scholarly journals The influence of active carbon contaminants on the ozonation mechanism interpretation

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lilla Fijołek ◽  
Joanna Świetlik ◽  
Marcin Frankowski
Keyword(s):  
Activated Carbon ◽  
Active Carbon ◽  
Alkali Metals ◽  
Activated Carbons ◽  
Carbon Surface ◽  
Bulk Solution ◽  
Ozone Decomposition ◽  
Reaction Products ◽  
Treatment Technology ◽  
Carbon Impurities

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.

scholarly journals Pinecone-Derived Activated Carbons as an Effective Medium for Hydrogen Storage

Energies ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2237
Author(s):  
Sara Stelitano ◽  
Giuseppe Conte ◽  
Alfonso Policicchio ◽  
Alfredo Aloise ◽  
Giovanni Desiderio ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Hydrogen Storage ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Hydrogen Adsorption ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Textural Properties ◽  
Biomass Waste ◽  
Wavelength Dispersive Spectrometry

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.

Adsorption of Soluble Metal Ions from Red Mud by Modified Activated Carbon

2008 ◽  
Vol 368-372 ◽  
pp. 1541-1544 ◽  
Author(s):  
Hua Lei Zhou ◽  
Dong Yan Li ◽  
Guo Zhuo Gong ◽  
Ya Jun Tian ◽  
Yun Fa Chen
Keyword(s):  
Activated Carbon ◽  
Metal Ions ◽  
Adsorption Capacity ◽  
Red Mud ◽  
Activated Carbons ◽  
Valuable Metal ◽  
Surface Areas ◽  
Alumina Industry ◽  
Modified Activated Carbons ◽  
Almost All

Activated carbon was employed as the adsorption carrier for the metal ions in HCl solution of red mud, a solid waste produced in alumina industry. To improve the adsorption capacity to valuable metal ions, the activated carbon was modified by chemicals including HNO3, H2O2, H2SO4, H3PO4, NH3, Na2CO3, and tri-butyl phosphate (TBP). It was found that the modifications contributed the high adsorption capacity to almost all metal ions we focused on. In the case of TBP, remarkably higher adsorption capacity and selectivity of Sc3+ was observed. The correlation between the surface areas, IR spectra of those chemically modified activated carbons and adsorption was schemed.

Effect of Fractal Dimension of Powder Activated Carbon on SO2 Adsorption

2014 ◽  
Vol 955-959 ◽  
pp. 2169-2172 ◽  
Author(s):  
Bing Li ◽  
Jian Ming Xue ◽  
Yue Yang Xu ◽  
Hong Liang Wang ◽  
Chun Yuan Ma ◽  
...  
Keyword(s):  
Fractal Dimension ◽  
Activated Carbon ◽  
Adsorption Capacity ◽  
Activated Carbons ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Removal Capacity ◽  
Powder Activated Carbon

Five kinds of powder activatedcarbons were studied to investigate the removal of SO2 from flue gasin a fixed bed reactor. The fractal dimension of activated carbon was determined by N2 adsorption isothermat 77Kand SO2 adsorptioncapacity was correlated with thefractal dimension. The results show thatthe activated carbons prepared from different precursors by differentactivation methods have different fractal dimension. Big differences in SO2 adsorption capacity are found between fivekinds of activated carbons. SO2 adsorption capacity increases with the fractaldimension increasing. The results indicate that the fractal dimension could be used as a indicator of SO2removal capacity on powder activated carbon.

Quinone/hydroquinone redox couple as a source of enormous capacitance of activated carbon electrodes

2013 ◽  
Vol 1505 ◽  
Author(s):  
Krzysztof Fic ◽  
Mikolaj Meller ◽  
Grzegorz Lota ◽  
Elzbieta Frackowiak
Keyword(s):  
Activated Carbon ◽  
Redox Reactions ◽  
Electrode Materials ◽  
Activated Carbons ◽  
Hydroxyl Group ◽  
Carbon Surface ◽  
Carbon Electrodes ◽  
Main Subject ◽  
Solution Ph ◽  
Reversible Redox

ABSTRACTThe main subject of this paper is to examine and to evaluate the capacitive behaviour of activated carbon electrodes electrochemically decorated by quinone-type functional groups. For this purpose, different electrolytes, i.e. hydroquinone, catechol and resorcinol at the concentration of 0.38 mol L-1, dissolved in 1 mol L-1 H2SO4, 1 mol L-1 Li2SO4 and 6 mol L-1 KOH were used. These electrolytes could generate electroactive groups (able to undergo reversible redox reactions) on the surface of electrode material. Apart from typical adsorption of the mentioned dihydroxybenzenes, so called grafting could occur and might cause generation of quinone|hydroquinone functionals on carbon surface. As an effect of functional reversible redox reaction, additional capacitance value, called pseudocapacitance, could be achieved. Hence, besides typical charge originating from charging/discharging of the electrical double layer on the electrode/electrolyte interface, additional capacitance comes also from faradaic reactions. Activated carbons are the most promising electrode materials for this purpose; apart from great physicochemical properties, they are characterized by well-developed specific surface area over 2000 m2 g-1 which results in high capacitance values.In the manuscript the influence of the hydroxyl group location as well as electrolyte solution pH on the electrochemical performance of the electrode is discussed.

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
Keyword(s):  
Activated Carbon ◽  
Low Temperature ◽  
Zinc Chloride ◽  
Sulphur Dioxide ◽  
Activated Carbons ◽  
Textural Properties ◽  
Nitrogen Adsorption ◽  
Carbon Surface ◽  
Steam Activation ◽  
Pore Widening

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.

Adsorption of cadmium(II) from aqueous solution onto activated carbon

1997 ◽  
Vol 35 (7) ◽  
pp. 205-211 ◽  
Author(s):  
R. Leyva-Ramos ◽  
J. R. Rangel-Mendez ◽  
J. Mendoza-Barron ◽  
L. Fuentes-Rubio ◽  
R. M. Guerrero-Coronado
Keyword(s):  
Activated Carbon ◽  
Adsorption Isotherm ◽  
Adsorption Capacity ◽  
Freundlich Isotherm ◽  
Carbon Surface ◽  
Maximum Adsorption Capacity ◽  
Solution Ph ◽  
Ph Values ◽  
Average Percent Deviation ◽  
Initial Ph

The adsorption isotherm of cadmium on activated carbon was measured in a batch adsorber. Effects of temperature and solution pH on the adsorption isotherm were investigated by determining the adsorption isotherm at temperatures of 10, 25, and 40°C and at initial pH values from 2 to 8. Langmuir isotherm better fitted the experimental data since the average percent deviation was lower than with the Freundlich isotherm It was noticed that the amount of Cd2+ adsorbed was reduced about 3 times by increasing the temperature from 10 to 40°C. It was found that Cd2+ was not adsorbed on activated carbon at pH of 2 or lower and that Cd2+ was precipitated out as Cd(OH)2 at pH values above 9. Maximum adsorption capacity was observed at pH of 8 and the adsorption capacity was decreased about 12 times by reducing the initial pH from 8 to 3. According to the cadmium speciation diagram the predominant species below pH of 8 is Cd2+. Thus, cadmium was adsorbed on the activated carbon surface as Cd2+. It was concluded that the adsorption capacity is a strong function of pH and temperature.

scholarly journals ADSORPSI ZAT WARNA METILEN BIRU DENGAN KARBON AKTIF DARI KULIT DURIAN MENGGUNAKAN KOH DAN NaOH SEBAGAI AKTIVATOR

2017 ◽  
Vol 6 (1) ◽  
pp. 49-55 ◽  
Author(s):  
Farida Hanum ◽  
Rikardo Jgst Gultom ◽  
Maradona Simanjuntak
Keyword(s):  
Activated Carbon ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Contact Time ◽  
Wavelength Region ◽  
Second Order ◽  
Carbon Surface ◽  
Maximum Adsorption Capacity ◽  
Activation Process ◽  
Maximum Surface

Durian is a kind of tropical fruits which can grow well in Indonesia. Durian is containing 60-75% shell. Durian shell could be a potential alternative to activated carbon because it contains 57.42% carbon. The aim of this research is to know the effect of contact time and  stirring speed to activated carbon adsorption capacity from durian shell with KOH and NaOH as activators. FTIR (Fourier Transform Infra Red) analysis showed the activation process effects on  absorption intensity  wavelength region and resulted in formation of C = C aromatic tape, so that the nature of the charcoal becomes more polar compared with the initial condition. Analysis using spectrophotometer UV-Vis to determine  absorbance and  final concentration of each variation of contact time and stirring speed. The results showed that the maximum adsorption capacity obtained by activation of KOH and NaOH on stirring speed of 150 rpm and a contact time of 90 minutes is equal to 3.92 mg / g and 3.8 mg / g respectively. The maximum surface area obtained by activation of KOH and NaOH during the stirring speed 130 rpm and a contact time of 120 minutes is equal to 1785.263 m2 / g and 1730.332 m2 / g respectively. The maximum surface area obtained from this research has met the standards of commercial activated carbon surface area was between 800-1800 m2/ g. Modeling pseudo second order presents a more representative adsorption data, a second order equation is based on the assumption that adsorption step is chemosorption.

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