scholarly journals Carbon Dioxide (CO2) Adsorption by Activated Carbon Functionalized with Deep Eutectic Solvent (DES)

Author(s):  
N Z Zulkurnai ◽  
U F Md. Ali ◽  
N Ibrahim ◽  
N S Abdul Manan
2018 ◽  
Vol 190 (7) ◽  
pp. 1259-1282 ◽  
Author(s):  
Umi Fazara Md Ali ◽  
Nur Hidayah Azmi ◽  
Khairuddin Md Isa ◽  
Mohamed Kheireddine Aroua ◽  
Tan Ru Shien ◽  
...  

Processes ◽  
2020 ◽  
Vol 8 (8) ◽  
pp. 941
Author(s):  
Jun Liu ◽  
Qiang Chen ◽  
Peng Qi

Upgrading raw biogas to methane (CH4) is a vital prerequisite for the utilization of biogas as a vehicle fuel or the similar field as well. In this work, biogas yield from the anaerobic fermentation of food waste containing methane (CH4, 60.4%), carbon dioxide (CO2, 29.1%), hydrogen sulfide (H2S, 1.5%), nitrogen (N2, 7.35%) and oxygen (O2, 1.6%) was upgraded by dynamic adsorption. The hydrogen sulfide was removed from the biogas in advance by iron oxide (Fe2O3) because of its corrosion of the equipment. Commercial 13X zeolite and carbon molecular sieve (CMS) were used to remove the other impurity gases from wet or dry biogas. It was found that neither 13X zeolite nor CMS could effectively remove each of the impurities in the wet biogas for the effect of water vapor. However, 13X zeolite could effectively remove CO2 after the biogas was dried with silica and showed a CO2 adsorption capacity of 78 mg/g at the condition of 0.2 MPa and 25 °C. Additionally, 13X zeolite almost did not adsorb nitrogen (N2), so the CH4 was merely boosted to ac. 91% after the desulfurated dry biogas passed through 13X zeolite, nitrogen remaining in the biogas. CMS would exhibit superior N2 adsorption capacity and low CO2 adsorption capacity if some N2 was present in biogas, so CMS was able to remove all the nitrogen and fractional carbon dioxide from the desulfurated dry biogas in a period of time. Finally, when the desulfurated dry biogas passed through CMS and 13X zeolite in turn, the N2 and CO2 were sequentially removed, and then followed the high purity CH4 (≥96%).


Processes ◽  
2019 ◽  
Vol 7 (11) ◽  
pp. 855 ◽  
Author(s):  
Azry Borhan ◽  
Suzana Yusup ◽  
Jun Wei Lim ◽  
Pau Loke Show

Global warming due to the emission of carbon dioxide (CO2) has become a serious problem in recent times. Although diverse methods have been offered, adsorption using activated carbon (AC) from agriculture waste is regarded to be the most applicable one due to numerous advantages. In this paper, the preparation of AC from rubber-seed shell (RSS), an agriculture residue through chemical activation using potassium hydroxide (KOH), was investigated. The prepared AC was characterized by nitrogen adsorption–desorption isotherms measured in Micrometrices ASAP 2020 and FESEM. The optimal activation conditions were found at an impregnation ratio of 1:2 and carbonized at a temperature of 700 °C for 120 min. Sample A6 is found to yield the largest surface area of 1129.68 m2/g with a mesoporous pore diameter of 3.46 nm, respectively. Using the static volumetric technique evaluated at 25 °C and 1.25 bar, the maximum CO2 adsorption capacity is 43.509 cm3/g. The experimental data were analyzed using several isotherm and kinetic models. Owing to the closeness of regression coefficient (R2) to unity, the Freundlich isotherm and pseudo-second kinetic model provide the best fit to the experimental data suggesting that the RSS AC prepared is an attractive source for CO2 adsorption applications.


2018 ◽  
Vol 34 ◽  
pp. 02030 ◽  
Author(s):  
N.Z. Zulkurnai ◽  
U.F. Md. Ali ◽  
N. Ibrahim ◽  
N.S. Abdul Manan

The increment amount of the CO2 emission by years has become a major concern worldwide due to the global warming issue. However, the influence modification of activated carbon (AC) has given a huge revolution in CO2 adsorption capture compare to the unmodified AC. In the present study, the Deep Eutectic Solvent (DES) modified surface AC was used for Carbon Dioxide (CO2) capture in the fixed-bed column. The AC underwent pre-carbonization and carbonization processes at 519.8 °C, respectively, with flowing of CO2 gas and then followed by impregnation with 53.75% phosphoric acid (H3PO4) at 1:2 precursor-to-activant ratios. The prepared AC known as sea mango activated carbon (SMAC) was impregnated with DES at 1:2 solid-to-liquid ratio. The DES is composing of choline chloride and urea with ratio 1:2 choline chloride to urea. The optimum adsorption capacity of SMAC was 33.46 mgco2/gsol and 39.40 mgco2/gsol for DES modified AC (DESAC).


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.


2014 ◽  
Vol 1024 ◽  
pp. 35-38
Author(s):  
Farah Diana Mohd Daud ◽  
Srimala Sreekantan ◽  
Abdul Rahman Mohamed

Carbon dioxide (CO2) is considered to be the main greenhouse gas contributing to global warming and climate change. Therefore, the present paper investigates the CO2-capture performance of synthesized calcium hydroxides, Ca(OH)2 sorbent at different temperatures which are 350, 450, 550 and 650°C. The CO2 adsorption of the materials synthesized was studied in a thermo-gravimetric analyzer (TGA). The CO2 adsorption temperature strongly influenced the capture performance of the absorbent. The Ca(OH)2 sorbent are prepared by hydrolysis of calcium alkoxides, NaOH as precipitating agent and mixed solvent of ethanol with deionized (DI) water as medium at 35°C. X- ray diffraction (XRD) result showed 40 nm crystallite size of Ca(OH)2 hexagonal crystal structures. The Ca(OH)2 particle size and morphological properties before and after CO2 adsorption are studied by Field Emission Scanning Electron Microscopy (FESEM). The FESEM image indeed showed the rod like shape of Ca(OH)2 structures with rod length increased from 765 to 893 nm while the diameter is between 140 to 160 nm. When Ca(OH)2 sorbent adsorbed CO2, the structures are rigid interconnected each others like a lump shaped. The prepared Ca(OH)2 sorbent possesses a great potential to capture CO2 when increased temperature. Nevertheless, at intermediate temperatures (350-450°C), Ca(OH)2 sorbent still demonstrates a higher CO2 capture capacity than other intermediate temperature adsorbents such as layered double hydroxides (LDHs), lithium zirconates (LiZrO3) and hydrotalcites.


2020 ◽  
Vol 230 ◽  
pp. 115571 ◽  
Author(s):  
Sima Sepahvand ◽  
Mehdi Jonoobi ◽  
Alireza Ashori ◽  
Florent Gauvin ◽  
H.J.H Brouwers ◽  
...  

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