scholarly journals Activated Carbons Tailored to Remove Different Pollutants from Gas Streams and from Solution

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.


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.


1995 ◽  
Vol 12 (3) ◽  
pp. 247-258 ◽  
Author(s):  
C. Nguyen ◽  
A. Ahmadpour ◽  
D.D. Do

Activated carbon was prepared from nut shells using a conventional two-stage method: carbonization followed by activation. Activation with steam or carbon dioxide as activating agent produced a range of chars of different burn-off. These were characterized for their total and micropore surface areas, and benzene adsorption capacity. Benzene adsorption measurement provided an insight into the effect of porosity development on the adsorptive properties of the adsorbent. It was found that activated carbon products from nut shells were comparable, in terms of adsorption characteristics, with activated carbons from other lignocellulosic precursors. The evolution of porosity of the resulting carbons shows that carbon dioxide is the preferable agent for the production of activated carbon with a narrow micropore size distribution.


2017 ◽  
Vol 19 (2) ◽  
pp. 44-50 ◽  
Author(s):  
Jarosław Serafin

Abstract The objective of this work was preparation of activated carbon from spent dregs for carbon dioxide adsorption. A saturated solution of KOH was used as an activating agent. Samples were carbonized in the furnace at the temperature of 550°C. Textural properties of activated carbons were obtained based on the adsorption-desorption isotherms of nitrogen at −196°C and carbon dioxide at 0°C. The specific surface areas of activated carbons were calculated by the Brunauer – Emmett – Teller equation. The volumes of micropores were obtained by density functional theory method. The highest CO2 adsorption was 9.54 mmol/cm3 at 0°C – and 8.50 mmol/cm3 at 25°C.


2021 ◽  
Vol 7 ◽  
Author(s):  
Prakash Parthasarathy ◽  
Hamish R. Mackey ◽  
Sabah Mariyam ◽  
Shifa Zuhara ◽  
Tareq Al-Ansari ◽  
...  

Bamboo is found worldwide but is especially concentrated in tropical and subtropical areas with the major producing nations being China, Indonesia and Thailand with an annual production of 12 million tonnes. It has found uses in many applications such as: furniture, flooring, roofing, fencing, interior design and scaffolding in the construction industry. In this study, discarded waste bamboo furniture was used in the ground form as the raw material feedstock for the production of a series of biochars and activated carbons. The biochars were produced at different temperatures, namely, 723, 823, 923, 1,023, 1,123 and 1223 K, in a muffle furnace inerted with nitrogen and for different pyrolysis times. The product chars yields were 20–30% by weight of the raw material, surface areas were 100–350 m2/g. Other tests include elemental analysis, helium displacement density, pH, ICP-AES on a leachate sample. Four of the different temperature samples of biochar were used to adsorb the basic dye methylene blue and were shown to possess high adsorption capacities. Then, the same bamboo raw material powder was treated with acid and pyrolysed/activated in a nitrogen atmosphere at the same range of temperatures to produce activated carbons; these were characterized using similar test methods to the biochars. The yields are in the range 20–40% by weight of the raw material feedstock and the BET surface areas are in the range 200–600 m2/g. Three of the different temperature activated carbons were used to adsorb methylene blue and the results were compared with the biochar results. All the adsorption experimental isotherm results were analyzed using conventional isotherm equations. The benefits and cost implications of both biochar and activated carbon routes are discussed. The methylene blue adsorption capacities are extremely attractive in the range 0.42–1.12 mmol/g (150–300 mg/g char product) and extend to over 2.35 mmol/g (700 mg/g) for the bamboo derived activated carbons. The micropore and mesopore volumes have been determined under the various char and activated carbon experimental conditions and coupled with the surface areas; these results have been used to explain the trends in the methylene blue adsorption capacities.


2011 ◽  
Vol 65 (2) ◽  
pp. 123-129 ◽  
Author(s):  
Milan Momcilovic ◽  
Milovan Purenovic ◽  
Milena Miljkovic ◽  
Aleksandar Bojic ◽  
Marjan Randjelovic

Horse chestnut kernel was used as the precursor for the preparation of powdered activated carbon using phosphoric acid as the activating agent. Batch adsorption experiments for the adsorption of cationic dye methylene blue from aqueous solutions were carried out using the obtained carbon as adsorbent. Equilibrium and kinetic experiments were conducted. The equilibrium data were fitted with the Langmuir, Freundlich and Temkin theoretical isotherm models. The best results was obtained in the case of Langmuir model, which indicates that monolayer adsorption occurs on finite number of the active adsorption sites on the carbon surface. The kinetic data were fitted with pseudo-first, pseudo-second, Elovich and interparticle diffusion model. Pseudo-second order model and Elovich model showed the best results of the kinetic data. The increasing of the solution pH led to a higher uptake of methylene blue due to the fact that competitive adsorption of methylene blue cation and proton exists in acidic solutions. The adsorption capacity for methylene blue in equilibrium study was significant (168.93 mg g-1). Comparison of the adsorption capacities of methylene blue onto activated carbons derived from various alternative precursors proves chestnut kernel to be efficient and low-cost material which could be substantially deployed in the future.


2018 ◽  
Vol 5 (1) ◽  
pp. 374
Author(s):  
David Wibowo ◽  
Lanny Setyadhi ◽  
Suryadi Ismadji

The adsorption behavior of activated carbons is determined not only by their porous structures but also by the chemical nature of its surface. The surface chemistry of activated carbons can be selectively modified in order to improve their adsorption capacity. In this study, a NORIT granular activated carbon was treated by oxidant (HNO3) and non-oxidant acid (HCI) at different concentrations and temperatures. The surface chemistries of the materials were characterized by Boehm titration method and by the determination of the point of zero charge (pHPZC).The adsorption properties of the selected samples were studied by adsorption of methylene blue, which is one of the important dyes and found in many textile effluents. In addition, the pore structures of the modified carbons were also studied by argon adsorption at 87.29 K. As results, it was observed that both HN03 and HCI treatments could increase the surface acidity of activated carbons. Activated carbons modified by HCI gave the best performance on the adsorption of methylene blue.Keywords: Activated Carbon, Surface Chemistry, Chemical Treatment, Boehm Titration Method, Adsorption AbstrakKemampuan adsorpsi karbon akti.ftidak hanya ditentukan oleh struktur pori tetapijuga dipengaruhi oleh sifat kimia dari permukaannya. Sifat kimia permukaan karbon aktif dapat secara selektif dimodifikasi dengan tujuan untuk lebih meningkatkan kapasitas adsorpsinya. Pada penelitian ini, karbon aktif NORIT granular ditreatment dengan menggunakan asam oksidator (HNO) dan non-oksidator (HCI) pada berbagai konsentrasi dan suhu. Sifat kimia permukaan karbon aktif dikarakterisasi dengan menggunakan metode titrasi Boehm serta dengan penentuan point of zero charge (pHPZC). Kemampuan adsorpsinya diuji dengan mengadsorp larutan methylene blue, dimana methylene blue merupakan salah satu komponen dalam limbah tekstil. Sedangkan struktur pori karbon aktif dianalisa dengan adsorpsi Ar pada suhu 87,29 K. Penelitian ini menunjukkan bahwa baik treatment dengan HNO3 maupun HCI dapat mengakibatkan terjadinya peningkatan sifat asam pada permukaan karbon aktif. Karbon aktif yang diberi perlalatan dengan HCI memberikan kemampuan adsorpsi yang paling baik dalam adsorpsi larutan methylen biru.Kata Kunci: Karbon Aktif, Sifat Kimia Permukaan, Perlakuan dengan Larutan Kimia, Metode Titrasi Boehm, Adsorpsi


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.  


2015 ◽  
Vol 8 (1) ◽  
pp. 8 ◽  
Author(s):  
Mohamad M. Diémé ◽  
Maxime Hervy ◽  
Saïdou N. Diop ◽  
Claire Gérente ◽  
Audrey Villot ◽  
...  

<p>The objective of this study was to investigate the production of activated carbons (AC) from cashew shells, and millet stalks and their efficiency in fluoride retention. These agricultural residues are collected from Senegal. It is known that some regions of Sénégal, commonly called the groundnut basin, are affected by a public health problem caused by an excess of fluoride in drinking water used by these populations. The activated carbons were produced by a combined pyrolysis and activation with water steam; no other chemical compounds were added. Then, activated carbonaceous materials obtained from cashew shells and millet stalks were called CS-H<sub>2</sub>O and MS-H<sub>2</sub>O respectively. CS-H<sub>2</sub>O and MS-H<sub>2</sub>O show very good adsorbent features, and present carbon content ranges between 71 % and 86 %. The BET surface areas are 942 m² g<sup>-1</sup> and 1234 m².g<sup>-1</sup> for CS-H<sub>2</sub>O and MS-H<sub>2</sub>O respectively. A third activated carbon produced from food wastes and coagulation-flocculation sludge (FW/CFS-H<sub>2</sub>O) was produced in the same conditions. Carbon and calcium content of FW/CFS-H<sub>2</sub>O are 32.6 and 39.3 % respectively. The kinetics sorption were performed with all these activated carbons, then the pseudo-first equation was used to describe the kinetics sorption. Fluoride adsorption isotherms were performed with synthetic and natural water with the best activated carbon from kinetics sorption, Langmuir and Freundlich models were used to describe the experimental data. The results showed that carbonaceous materials obtained from CS-H<sub>2</sub>O and MS-H<sub>2</sub>O were weakly efficient for fluoride removal. With FW/CFS-H<sub>2</sub>O, the adsorption capacity is 28.48 mg.g<sup>-1 </sup>with r² = 0.99 with synthetic water.</p>


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