scholarly journals Activated Carbons from Crosslinked Novolac Resin

2005 ◽  
Vol 23 (5) ◽  
pp. 381-386
Author(s):  
Janusz Pajak ◽  
Grzegorz Labojko ◽  
Andrzej Lachowski

Activated carbons were prepared from well-characterized Novolac resin cured with various amounts of hexamethylenetetramine (HMTA). The process consisted of curing the resin with HMTA at 200°C, carbonization in nitrogen at 600°C and gasifying the char in carbon dioxide or in steam at 900°C. The influence of the amount of HMTA used for curing on the yield and the characteristics of the activated carbon was investigated. The pore volume attained a maximum for Novolac initially cured with ca. 2 wt% HMTA. Further increase in the amount of HMTA used for curing resulted in an increase in the yield of active carbon, but the susceptibility to carbon dioxide activation decreased. Relative to carbon dioxide, the use of steam generated a narrower, but more extensive, microporosity in the char obtained from cured Novolac resin.

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.


2006 ◽  
Vol 23 (6) ◽  
pp. 1046-1054 ◽  
Author(s):  
Yuvarat Ngernyen ◽  
Chaiyot Tangsathitkulchai ◽  
Malee Tangsathitkulchai

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
N. Mojoudi ◽  
N. Mirghaffari ◽  
M. Soleimani ◽  
H. Shariatmadari ◽  
C. Belver ◽  
...  

AbstractThe purpose of this study was the preparation, characterization and application of high-performance activated carbons (ACs) derived from oily sludge through chemical activation by KOH. The produced ACs were characterized using iodine number, N2 adsorption-desorption, Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The activated carbon prepared under optimum conditions showed a predominantly microporous structure with a BET surface area of 2263 m2 g−1, a total pore volume of 1.37 cm3 g−1 and a micro pore volume of 1.004 cm3 g−1. The kinetics and equilibrium adsorption data of phenol fitted well to the pseudo second order model (R2 = 0.99) and Freundlich isotherm (R2 = 0.99), respectively. The maximum adsorption capacity based on the Langmuir model (434 mg g−1) with a relatively fast adsorption rate (equilibrium time of 30 min) was achieved under an optimum pH value of 6.0. Thermodynamic parameters were negative and showed that adsorption of phenol onto the activated carbon was feasible, spontaneous and exothermic. Desorption of phenol from the adsorbent using 0.1 M NaOH was about 87.8% in the first adsorption/desorption cycle and did not decrease significantly after three cycles. Overall, the synthesized activated carbon from oily sludge could be a promising adsorbent for the removal of phenol from polluted water.


2016 ◽  
Vol 35 (6) ◽  
pp. 535-541 ◽  
Author(s):  
Hongying Xia ◽  
Jian Wu ◽  
Chandrasekar Srinivasakannan ◽  
Jinhui Peng ◽  
Libo Zhang

AbstractThe present work attempts to convert bamboo into a high surface area activated carbon via microwave heating. Different chemical activating agents such as KOH, NaOH, K2CO3 and Na2CO3 were utilized to identify a most suitable activating agent. Among the activating agents tested KOH was found to generate carbon with the highest porosity and surface area. The effect of KOH/C ratio on the porous nature of the activated carbon has been assessed. An optimal KOH/C ratio of 4 was identified, beyond which the surface area as well as the pore volume were found to decrease. At the optimized KOH/C ratio the surface area and the pore volume were estimated to be 3,441 m2/g and 2.093 ml/g, respectively, with the significant proportion of which being microporous (62.3%). Activated carbon prepared under the optimum conditions was further characterized using Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). Activated carbons with so high surface area and pore volume are very rarely reported, which could be owed to the nature of the precursor and the optimal conditions of mixture ratio adopted in the present work.


2019 ◽  
Vol 2 (3) ◽  
pp. 1205-1209
Author(s):  
Hasan Sayğılı

The influence of carbonization temperature (CT) on pore properties of the prepared activated carbon using lentil processing waste product (LWP) impregnated with potassium carbonate was studied. Activated carbons (ACs) were obtained by impregnation with 3:1 ratio (w/w) K2CO3/LWP under different carbonization temperatures at 600, 700, 800 and 900 oC for 1h. Activation at low temperature represented that micropores were developed first and then mesoporosity developed, enhanced up to 800 oC and then started to decrease due to possible shrinking of pores. The optimum temperature for LWP was found to be around 800 oC on the basis of total pore volume and the Brunauer-Emmett-Teller (BET) surface area. The optimum LWPAC sample was found with a CT of 800 oC, which gives the highest BET surface area and pore volume of 1875 m2/g and 0.995 cm3/g, respectively.


2019 ◽  
Vol 62 (6) ◽  
pp. 1435-1445 ◽  
Author(s):  
Saravanan Ramiah Shanmugam ◽  
Sushil Adhikari ◽  
Hyungseok Nam ◽  
Vivek Patil

HighlightsGlyphosate sorption using bio-based adsorbents was investigated in this study.Biochars showed poor sorption of glyphosate in comparison to the activated carbons.Total pore volume of bio-based adsorbents played a key role in sorption of glyphosate.Abstract. This study examined the glyphosate sorption ability of different bio-based materials, including biochars and activated carbons synthesized from Douglas fir, kraft lignin, and mixed wood pellets. All the biochars showed poor sorption of glyphosate in comparison to the activated carbons derived from biochars and the commercial powdered activated carbon (PAC) investigated in this study. All the biochar-derived activated carbons produced in the laboratory showed comparable glyphosate sorption in comparison to PAC. The activated carbons synthesized from Douglas fir biomass showed the highest glyphosate sorption among the activated carbons investigated. Langmuir and Freundlich isotherms were used to describe the adsorption kinetics of glyphosate onto activated carbons. Adsorption capacity showed better correlation (R2 = 0.989) with the total pore volume in comparison to the Brunauer-Emmett-Teller (BET) surface area and microporosity. The results of batch desorption tests indicated that the biochar-derived activated carbons and PAC showed >60% glyphosate retention. The results of this study indicate that activated carbons derived from biochars produced with thermochemical conversion processes could effectively sorb herbicide such as glyphosate similarly to commercial activated carbon and could be used either as a replacement for PAC in water treatment plants or for on-site treatment of agricultural runoff water. Keywords: Adsorption, Desorption, Herbicides, Kraft lignin, Model isotherms, Pore volume.


2019 ◽  
Vol 9 (10) ◽  
pp. 1977 ◽  
Author(s):  
Yu-Chun Chiang ◽  
Cheng-Yu Yeh ◽  
Chih-Hsien Weng

Polyacrylonitrile-based activated carbon fibers (ACFs), modified using potassium hydroxide (KOH) or tetraethylenepentamine (TEPA), were investigated for carbon dioxide (CO2) adsorption, which is one of the promising alleviation approaches for global warming. The CO2 adsorption isotherms were measured, and the values of isosteric heat of adsorption were calculated. The results showed that the KOH-modified ACFs exhibited a great deal of pore volume, and a specific surface area of 1565 m2/g was obtained. KOH activation made nitrogen atoms easily able to escape from the surface of ACFs. On the other hand, the surface area and pore volume of ACFs modified with TEPA were significantly reduced, which can be attributed to the closing or blocking of micropores by the N-groups. The CO2 adsorption on the ACF samples was via exothermic reactions and was a type of physical adsorption, where the CO2 adsorption occurred on heterogeneous surfaces. The CO2 uptakes at 1 atm and 25 °C on KOH-activated ACFs reached 2.74 mmole/g. This study observed that microporosity and surface oxygen functionalities were highly associated with the CO2 uptake, implying the existence of O-C coordination, accompanied with physical adsorption. Well cyclability of the adsorbents for CO2 adsorption was observed, with a performance decay of less than 5% over up to ten adsorption-desorption cycles.


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.


Energies ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 3136 ◽  
Author(s):  
Deneb Peredo-Mancilla ◽  
Imen Ghouma ◽  
Cecile Hort ◽  
Camelia Matei Ghimbeu ◽  
Mejdi Jeguirim ◽  
...  

The aim of the present work is to study the effect of different activation methods for the production of a biomass-based activated carbon on the CO 2 and CH 4 adsorption. The influence of the activation method on the adsorption uptake was studied using three activated carbons obtained by different activation methods (H 3 PO 4 chemical activation and H 2 O and CO 2 physical activation) of olive stones. Methane and carbon dioxide pure gas adsorption experiments were carried out at two working temperatures (303.15 and 323.15 K). The influence of the activation method on the adsorption uptake was studied in terms of both textural properties and surface chemistry. For the three adsorbents, the CO 2 adsorption was more important than that of CH 4 . The chemically-activated carbon presented a higher specific surface area and micropore volume, which led to a higher adsorption capacity of both CO 2 and CH 4 . For methane adsorption, the presence of mesopores facilitated the diffusion of the gas molecules into the micropores. In the case of carbon dioxide adsorption, the presence of more oxygen groups on the water vapor-activated carbon enhanced its adsorption capacity.


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