Simultaneous activation/sulfurization method for production of sulfurized activated carbons: characterization and Hg(II) adsorption capacity

2013 ◽  
Vol 69 (3) ◽  
pp. 546-552 ◽  
Author(s):  
Hadi ShamsiJazeyi ◽  
Tahereh Kaghazchi
Keyword(s):  
Specific Surface ◽  
Adsorption Capacity ◽  
Activated Carbons ◽  
Nitrogen Adsorption ◽  
Surface Charges ◽  
Ph Values ◽  
Surface Areas ◽  
Simultaneous Activation ◽  
Adsorption Desorption ◽  
Significant Attention

As an inexpensive method for modification of activated carbons (ACs), sulfurization has attracted significant attention. However, the resulting sulfurized activated carbons (SACs) often are less porous than the original ACs. In this work, we propose a new method for concurrent sulfurization/activation that can lead to preparation of SACs with more porosity than the corresponding non-sulfurized ACs. By using scanning electron microscopy, nitrogen adsorption/desorption, and iodine number experiments, the porous structure of the SACs has been compared with that of non-sulfurized ACs. The specific surface areas of SACs are higher than the corresponding ACs, regardless of the type of activation agents used. For instance, the specific surface area of SAC and AC activated with phosphoric acid is 1,637 and 1,338 m2/g, respectively. Additionally, sulfur contents and surface charges (pHpzc) of the SACs and non-sulfurized ACs are compared. In fact, the SACs have higher sulfur contents and more acidic surfaces. Furthermore, the Hg(II) adsorption capacity of SACs has been compared with the corresponding non-sulfurized ACs. The Hg(II) adsorption isotherms on a selected SAC is measured at different pH values and temperatures. Hg(II) adsorptions as high as 293 mg/g are observed by using SACs prepared by the method proposed in this study.

scholarly journals Sorption of Methylene Blue for Studying the Specific Surface Properties of Biomass Carbohydrates

Coatings ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1115
Author(s):  
Tatiana Skripkina ◽  
Ekaterina Podgorbunskikh ◽  
Aleksey Bychkov ◽  
Oleg Lomovsky
Keyword(s):  
Methylene Blue ◽  
Specific Surface ◽  
Surface Area ◽  
Surface Characterization ◽  
Gas Adsorption ◽  
Comparative Method ◽  
Nitrogen Adsorption ◽  
Surface Areas ◽  
Nitrogen Adsorption Isotherms ◽  
Adsorption Desorption

The surface area is an important parameter in setting any biorefining technology. The aim of this study was to investigate the applicability of sorption of methylene blue to characterize the surface of the main biomass carbohydrates: α-cellulose, sigmacell cellulose, natural gum, β-glucan, and starch. The morphology of particles of the model objects was studied by scanning electron microscopy. Nitrogen adsorption isotherms demonstrate that the selected carbohydrates are macroporous adsorbents. The monolayer capacities, the energy constants of the Brunauer–Emmett–Teller (BET) equation, and specific surface areas were calculated using the BET theory, the comparative method proposed by Gregg and Sing, and the Harkins–Jura method. The method of methylene blue sorption onto biomass carbohydrates was adapted and mastered. It was demonstrated that sorption of methylene blue proceeds successfully in ethanol, thus facilitating surface characterization for carbohydrates that are either soluble in water or regain water. It was found that the methylene blue sorption values correlate with specific surface area determined by nitrogen adsorption/desorption and calculated from the granulometric data. As a result of electrostatic attraction, the presence of ion-exchanged groups on the analyte surface has a stronger effect on binding of methylene blue than the surface area does. Sorption of methylene blue can be used in addition to gas adsorption/desorption to assess the accessibility of carbohydrate surface for binding large molecules.

scholarly journals Characterization of Chemically Activated Carbons Prepared from Miscanthus and Switchgrass Biomass

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1654 ◽  
Author(s):  
Beata Doczekalska ◽  
Monika Bartkowiak ◽  
Bogusława Waliszewska ◽  
Grażyna Orszulak ◽  
Joanna Cerazy-Waliszewska ◽  
...  
Keyword(s):  
Activated Carbons ◽  
Nitrogen Adsorption ◽  
Crop Species ◽  
Alternative Source ◽  
Surface Oxygen Groups ◽  
Surface Areas ◽  
Oxygen Groups ◽  
Adsorption Desorption ◽  
Chemical Groups

Lignocellulosic biomass, including that of energy crops, can be an alternative source to produce activated carbons (ACs). Miscanthus and switchgrass straw were used to produce ACs in a two-step process. Crushed plant material was carbonized at 600 °C and then obtained carbon was activated using NaOH or KOH at 750 °C. The content of surface oxygen groups was determined using Boehm’s method. The porosity of ACs was assayed using the nitrogen adsorption/desorption technique, while their thermal resistance using the thermogravimetric method. The ACs derived from miscanthus and switchgrass were characterized by surfaces rich in chemical groups and a highly developed porous structure. The highest specific surface areas, over 1600 m2/g, were obtained after carbon treatment with NaOH. High values of iodine number, 1200–1240 mg/g, indicate an extensive system of micropores and their good adsorption properties. The type of activator affected the contents of oxygen functional groups and some porosity parameters as well as thermal stability ranges of the ACs. Among obtained carbons, the highest quality was found for these derived from M. sacchariflorus followed by switchgrass, after activation with NaOH. Hence, while these crop species are not as effective biomass sources as other energy grasses, they can become valuable feedstocks for ACs.

Sorption Behaviour of Waste-Generated Trace Metals in Estuarine Waters

1988 ◽  
Vol 20 (6-7) ◽  
pp. 113-121 ◽  
Author(s):  
G. A. Glegg ◽  
J. G. Titley ◽  
G. E. Millward ◽  
D. R. Glasson ◽  
A. W. Morris
Keyword(s):  
Specific Surface ◽  
Toxic Metal ◽  
Nitrogen Adsorption ◽  
Turbidity Maximum ◽  
Tamar Estuary ◽  
Sorption Behaviour ◽  
Surface Areas ◽  
Adsorption Desorption ◽  
Mn Oxides

Samples of suspended particles have been collected from the turbidity maximum region of the Tamar Estuary, S.W. England. Specific surface areas and porosities of the particles were determined by a BET nitrogen adsorption technique. The role of surface coatings of organic matter and Fe and Mn oxides was examined. The data show that the specific surface area was highest at the turbidity maximum and was associated with high Fe/Mn ratios. The characterised particles were then used in time-dependent adsorption-desorption experiments, with waters from the metal-rich Carnon River, S.W. England. The rates and extents of the sorption processes were interpreted in terms of a two-stage reaction which was related to the microstructures of the particles. Kinetic analyses of the desorption profiles gave rate constants which are of significance in the prediction of the fate of toxic metal wastes discharged into estuaries.

Synthesis of Novel Core-Shell Structured Hydroxyapatite/Meso-Silica for Removal of Methylene Blue from Aqueous Solutions

2012 ◽  
Vol 463-464 ◽  
pp. 543-547 ◽  
Author(s):  
Cheng Feng Li ◽  
Xiao Lu Ge ◽  
Shu Guang Liu ◽  
Fei Yu Liu
Keyword(s):  
Methylene Blue ◽  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Low Cost ◽  
Nitrogen Adsorption ◽  
Precipitation Method ◽  
Core Shell ◽  
Adsorption Desorption

Core-shell structured hydroxyapatite (HA)/meso-silica was prepared and used as absorbance of methylene blue (MB). HA/meso-silica was synthesized in three steps: preparation of nano-sized HA by wet precipitation method, coating of dense silica and deposition of meso-silica shell on HA. As-received samples were characterized by Fourier transformed infare spectra, small angle X-ray diffraction, nitrogen adsorption-desorption isotherm and transmission electron microscopy. A wormhole framework mesostructure was found for HA/meso-silica. The specific surface area and pore volume were 128 m2•g-1 and 0.36 cm3•g-1, respectively. From the adsorption isotherm, HA/meso-silica with the great specific surface area exhibited a prominent adsorption capacity of MB (134.0 mg/g) in comparison with bare HA (0 mg/g). This study might shed light on surface modification of conventional low-cost adsorbents for removal of organic pollutants from aqueous solutions.

Optimization of Production Conditions for Activated Carbons from Rice Husk by Potassium Carbonate Using Response Surface Methodology

2014 ◽  
Vol 1053 ◽  
pp. 303-310 ◽  
Author(s):  
Mian Wu Meng ◽  
Cong Liang Qi ◽  
Qing Ye Liu ◽  
Liang Lv ◽  
Hao Ai ◽  
...  
Keyword(s):  
Response Surface Methodology ◽  
Adsorption Capacity ◽  
Response Surface ◽  
Rice Husk ◽  
Activated Carbons ◽  
Total Pore Volume ◽  
Nitrogen Adsorption ◽  
Average Pore ◽  
Activation Temperature ◽  
Nitrogen Adsorption Isotherm

A three-factor-three-level experiment was developed by the central composite design (CCD) and Response surface methodology to discuss the effects of concentration of K2CO3, activation temperature and time on the adsorption capacity of the activated carbon (AC) derived from the rice husk and to identify the key preparation parameters. The performance of the AC was characterized by nitrogen adsorption isotherm as Brunauer–Emmett–Teller (BET) and scanning electron microscope (SEM), respectively. The optimal parameters were obtained: Rice husk was soaked in K2CO3 solution (2.32 mol/L) with an impregnation ratio (rice husk: K2CO3=1:3) (wt. %), activated at 1239 K for 0.48 h. The results showed that iodine adsorption capacity of the AC was 1268.52 mg/g, the error between the models predicted (1356.98 mg/g) was only 6.2%. The AC has a large apparent surface area (SBET = 1312 m2/g), total pore volume (0.78 cm3/g) and average pore diameter (11.92 Å).

Structural and surface aspects of thermally treated copper aluminium mixed hydroxides

1991 ◽  
Vol 69 (10) ◽  
pp. 1511-1515 ◽  
Author(s):  
Awad I. Ahmed ◽  
S. E. Samra ◽  
S. A. El-Hakam
Keyword(s):  
Pore Structure ◽  
Copper Content ◽  
Textural Properties ◽  
Nitrogen Adsorption ◽  
Phase Changes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Areas ◽  
Structure Surface ◽  
Adsorption Desorption

CuO–Al2O3 catalysts containing various amounts of copper oxide have been prepared by precipitation. The phase changes were studied by X-ray diffraction. The results obtained revealed that the thermal treatment of solid CuO–Al2O3 at 700 °C produced only crystalline CuO. Heating to 900 °C led to the formation of copper alumina spinel together with unreacted CuO and γ-Al2O3. The spinel content was found to increase with increasing copper content. Nitrogen adsorption–desorption isotherms on the calcined samples have been measured. Surface areas have been calculated and the pore structure analysed. The textural properties of the system were found to depend on both the copper content and the calcination temperature. Key words: CuO, Al2O3 catalysts, structure, surface area, pore structure.

scholarly journals Catalytic Decomposition of H2O2 over Pure and Li2O-Doped Co3O4 Solids

1998 ◽  
Vol 16 (9) ◽  
pp. 733-746 ◽  
Author(s):  
Gamil A. El-Shobaky ◽  
Nagi R.E. Radwan ◽  
Farouk M. Radwan
Keyword(s):  
Heat Treatment ◽  
Specific Surface ◽  
Catalytic Decomposition ◽  
Nitrogen Adsorption ◽  
Progressive Increase ◽  
Lithium Oxide ◽  
Lithium Nitrate ◽  
Surface Areas ◽  
Catalytically Active ◽  
Cobaltic Oxide

Pure and doped Co3O4 samples were prepared by the thermal decomposition at 500–900°C of pure and lithium nitrate-treated basic cobalt carbonate. The amounts of dopant added were varied in the range 0.75–6 mol% Li2O. The effects of this treatment on the surface and catalytic properties of cobaltic oxide solid were investigated using nitrogen adsorption at −196°C and studies of the decomposition of H2O2 at 30–50°C. The results obtained revealed that Li2O doping of Co3O4 followed by heat treatment at 500°C and 600°C resulted in a progressive increase in the value of the specific surface area, SBET, to an extent proportional to the amount of dopant present. However, the increase was more pronounced in the case of solid samples calcined at 500°C. This increase in the specific surface areas has been attributed to the fixation of a portion of the dopant ions on the uppermost surface layers of the solid leading to outward growth of the surface lattice. The observed increase in SBET due to Li2O doping at 500°C might also result from a narrowing of the pores in the treated solid as a result of the doping process. Lithium oxide doping of cobaltic oxide followed by heat treatment at 700–900°C resulted in a significant decrease in the SBET, Vp and r̄ values. Pure and doped solids precalcined at 500°C and 600°C exhibited extremely high catalytic activities which were not much affected by doping with Li2O. On the other hand, doping followed by calcination at 700–900°C brought about a considerable and progressive increase in the catalytic activity of the treated solids. This treatment did not modify the activation energy of the catalysed reaction, i.e. doping of Co3O4 solid followed by heating at 700°C and 900°C did not alter the mechanism of the catalytic reaction but increased the concentration of catalytically active constituents taking part in the catalytic process without altering their energetic nature.

Removal of Cu, Fe, and Zn from Peat Water by Using Activated Carbon Derived from Oil Palm Leaves

2021 ◽  
Vol 1162 ◽  
pp. 65-73
Author(s):  
Rakhmawati Farma ◽  
Ona Lestari ◽  
Erman Taer ◽  
Apriwandi ◽  
Minarni ◽  
...  
Keyword(s):  
Heavy Metal ◽  
Activated Carbon ◽  
Oil Palm ◽  
Activated Carbons ◽  
Nitrogen Adsorption ◽  
Surface Characteristics ◽  
Batch Adsorption ◽  
X Ray ◽  
Turbidity Level ◽  
Adsorption Desorption

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.

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.

Effects of Carbonation on the Specific Surface BET of Cement Mortar Measured by Two Different Methods: Nitrogen Adsorption and Water Adsorption

2014 ◽  
Vol 931-932 ◽  
pp. 421-425 ◽  
Author(s):  
Son Tung Pham ◽  
William Prince
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Water Adsorption ◽  
Cement Mortar ◽  
Nitrogen Adsorption ◽  
Accelerated Carbonation ◽  
Molecular Sizes ◽  
The Difference ◽  
Adsorption Desorption

The objective of this work was to examine the microstructural changes caused by the carbonation of normal mortar. Samples were prepared and subjected to accelerated carbonation at 20°C, 65% relative humidity and 20% CO2concentration. The evolutions of the pore size distribution and the specific surface area during carbonation were calculated from the adsorption - desorption isotherms of water vapour and nitrogen. Conflicts observed in the results showed that the porous domains explored by these two methods are not the same due to the difference in molecular sizes of nitrogen and water. These two techniques therefore help to complementarily evaluate the effects of carbonation. The study also helped to explain why results in the literature diverge greatly on the influence of carbonation on specific surface area.

Sign in / Sign up

Export Citation Format

Share Document