scholarly journals Covalent triazine-based frameworks (CTFs) from triptycene and fluorene motifs for CO2 adsorption

2016 ◽  
Vol 4 (17) ◽  
pp. 6259-6263 ◽  
Author(s):  
Subarna Dey ◽  
Asamanjoy Bhunia ◽  
Dolores Esquivel ◽  
Christoph Janiak
Keyword(s):  
Carbon Dioxide ◽  
Surface Area ◽  
Co2 Adsorption ◽  
Uptake Capacity ◽  
Carbon Dioxide Uptake

Two microporous CTFs with triptycene (TPC) and fluorene (FL) have been synthesized through a mild AlCl3-catalyzed Friedel–Crafts reaction, with the highest surface area of up to 1668 m2 g−1 for non-ionothermal CTFs. CTF-TPC and CTF-FL show an excellent carbon dioxide uptake capacity of up to 4.24 mmol g−1 at 273 K and 1 bar.

scholarly journals Carbon Dioxide Adsorption on Porous and Functionalized Activated Carbon Fibers

2019 ◽  
Vol 9 (10) ◽  
pp. 1977 ◽  
Author(s):  
Yu-Chun Chiang ◽  
Cheng-Yu Yeh ◽  
Chih-Hsien Weng
Keyword(s):  
Carbon Dioxide ◽  
Activated Carbon ◽  
Surface Area ◽  
Carbon Fibers ◽  
Pore Volume ◽  
Co2 Adsorption ◽  
Physical Adsorption ◽  
Koh Activation ◽  
Co2 Uptake ◽  
Activated Carbon Fibers

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.

scholarly journals Defining a performance map of porous carbon sorbents for high-pressure carbon dioxide uptake and carbon dioxide–methane selectivity

2016 ◽  
Vol 4 (38) ◽  
pp. 14739-14751 ◽  
Author(s):  
Saunab Ghosh ◽  
Marta Sevilla ◽  
Antonio B. Fuertes ◽  
Enrico Andreoli ◽  
Jason Ho ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
High Pressure ◽  
Pore Volume ◽  
Carbon Materials ◽  
Total Pore Volume ◽  
Uptake Capacity ◽  
Heteroatom Doping ◽  
Carbon Dioxide Uptake ◽  
Performance Map ◽  
Methane Selectivity

The relative influence of heteroatom doping, surface area, and total pore volume of highly microporous carbon materials on CO2 uptake capacity, and the CO2/CH4 selectivity, at high pressure (≤30 bar) is presented.

scholarly journals Synthesis of FeCo-MIL-88B and Investigate Its Potential for CO2 Capture

2019 ◽  
Vol 35 (1) ◽  
Author(s):  
Le Minh Cam ◽  
Le Van Khu ◽  
Nguyen Thi Thu Ha ◽  
Nguyen Ngoc Ha
Keyword(s):  
Carbon Dioxide ◽  
Surface Area ◽  
Mesoporous Materials ◽  
Co2 Capture ◽  
Carbon Capture ◽  
Co2 Adsorption ◽  
Carbon Dioxide Capture ◽  
Metal Organic Framework ◽  
Metal Organic ◽  
Organic Framework

Cobalt dopping Fe-MIL-88B were successfully synthesized -in solvothermal procedure using DMF as solvent and with/without NaOH. The samples were characterized using SEM, BET and TGA techniques. The partly substitution of Fe by Co does not change the octahedral shape of their parent Fe-MIL-88B. Crystallizations conducted in NaOH medium, however, results in rod like with 2-end octahedral shape crystals. The BET specific surface area is 139cm2/g. The TGA data indicated that the presence of Co resulted in an increase in thermal stability of synthesized samples compared to parent Fe-MIL-88B. The CO2 adsorption isotherms in Fe-MIL-88B-Co samples were measured volumetrically at five temperatures:278K, 288K, 298K, 308K, 318K. The obtained results showed that Fe-MIL-88B-Co is a potential adsorbent with a maximum adsortption capacity of 1.2312 mmol/g (at T= 278K). The sample synthesized in alkali medium exhibited a better adsorbent for CO2 storage. Keywords MIL, adsorption, CO2 References [1] S. Chu, Carbon Capture and Sequestration, Science325(2009)1599 [2] R.S. Haszeldine,Carbon Capture and Storage: How Green Can Black Be?, Science325(2009) 1647[3] D.M. D’Alessandro, B. Smit, J.R. Long,Carbon Dioxide Capture: Prospects for New Materials, Angewandte Chemie International Edition. 49(2010) 6058[4] S. Bai, J. Liu, J. Gao, Q. Yang Can Li,Hydrolysis controlled synthesis of amine-functionalized hollow ethane–silica nanospheres as adsorbents for CO2 capture, Microporous and Mesoporous Materials151(2012) 474[5] K. Sumida, D.L. Rogow, J.A. Mason, T.M. McDonald, E.D. Bloch, Z.R. Herm, T.H. Bae, J.R.[6] Long,Carbon Dioxide Capture in Metal–Organic Frameworks, Chemical Reviews, 112(2012) 724[7] J.D. Carruthers, M.A. Petruska, E.A. Sturm, S.M. Wilson,Molecular sieve carbons for CO2 capture, Microporous and Mesoporous Materials,154 (2012) 62[8] X. Yan, L. Zhang, Y. Zhang, K. Qiao, Z. Yan, S. Komarneni,Amine-modified mesocellular silica foams for CO2 capture, Chemical Engineering Journal,168 (2011), 918[9] A. Zukal, C.O. Arean, M.R. Delgado, P. Nachtigall, A. Pulido, J. Mayerova, J. Cˇejka,Combined volumetric, infrared spectroscopic and theoretical investigation of CO2 adsorption on Na-A zeolite,Microporous and Mesoporous Materials 146 (2011) 97[10] S. Keskin, T.M. van Heest, D.S. Sholl, Can Metal–Organic Framework Materials Play a Useful Role in Large‐Scale Carbon Dioxide Separations?, ChemSusChem3 (2010) 879[11] T.M. McDonald, W.R. Lee, J.A. Mason, B.M. Wiers, C.S. Hong, J.R. Long, Capture of Carbon Dioxide from Air and Flue Gas in the Alkylamine-Appended Metal–Organic Framework mmen-Mg2(dobpdc), Journal of the American Chemical Society134 (2012) 7056[12] X. Yan, S. Komarneni, Z. Zhang, Z. Yan(2014),Extremely enhanced CO2 uptake by HKUST-1 metal–organic framework via a simple chemical treatment, Microporous and Mesoporous Materials183 (2014) 69–73[13] Gia-Thanh Vuong, Minh-Hao Pham and Trong-On Do*, Direct synthesis and mechanism of the formation of mixed metal Fe2Ni-MIL-88B†, CrystEngComm, DOI: 10.1039/c3ce41453a[14] Lê Văn Khu, Nguyễn Quốc Anh, Nguyễn Ngọc Hà, Lê Minh Cầm, Tổng hợp, đặc trưng và khảo sát khả năng hấp phụ CO2 của Fe-MIL-88B, Tạp chí xúc tác và hấp phụ 4 (1) (2015) 52[15] K. S. W. Sing, D. H. Everett, R. A. W. Hau et.al, Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity, Pure and Applied Chemistry 57 (1985) 603

scholarly journals Adsorption of carbon dioxide on MIL53(Al), CuBTC and K- NaX zeolite

2020 ◽  
Vol 4 (3) ◽  
pp. 30-42
Author(s):  
Fehime Cakicioglu-Ozkan
Keyword(s):  
Carbon Dioxide ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Co2 Adsorption ◽  
Ultrasonic Method ◽  
Metal Organic Frameworks ◽  
Isosteric Heat ◽  
Metal Organic ◽  
Increasing Temperature

CO2 adsorption on K exchanged NaX zeolites, and metal organic frameworks (MOFs), namely Cu-BTC and MIL53 (Al) was studied at 5 °C and 25 °C.  Exchange via ultrasonic and traditional methods, was conducted at 50 °C and 70 °C. The maximum replacement of Na+ ion with K+ ion in the extra framework of zeolite was increased from 76% to 83% with increasing temperature from 50 °C to 70 °C in the ultrasonic method which is more effective than traditional one. Compared with the zeolites, the MOF adsorbents used in this work have higher Langmuir specific surface area values namely 1278, 1473 and about 1000 m2/g for MIL 53, Cu-BTC and zeolite adsorbents respectively. The resulting CO2 isotherms can be well represented by the Toth equation. Comparison of the isosteric heat of adsorption at zero loading shows that CO2 was adsorbed more weakly on MOFs than zeolites.

A triazine-based covalent organic polymer for efficient CO2 adsorption

2015 ◽  
Vol 51 (49) ◽  
pp. 10050-10053 ◽  
Author(s):  
Ruth Gomes ◽  
Piyali Bhanja ◽  
Asim Bhaumik
Keyword(s):  
Schiff Base ◽  
Surface Area ◽  
Co2 Adsorption ◽  
Condensation Reaction ◽  
Organic Polymer ◽  
Bet Surface Area ◽  
Uptake Capacity ◽  
Hexagonally Ordered

A new triazine functionalized hexagonally ordered covalent organic polymer (TRITER-1) with a high BET surface area (716 m2 g−1) has been synthesized via the Schiff-base condensation reaction between a triamine and terephthaldehyde. TRITER-1 shows an excellent CO2 uptake capacity of 58.9 wt% at 273 K and 5 bar pressure.

scholarly journals New Porous Silicon-Containing Organic Polymers: Synthesis and Carbon Dioxide Uptake

Processes ◽  
2020 ◽  
Vol 8 (11) ◽  
pp. 1488
Author(s):  
Safaa H. Mohamed ◽  
Ayad S. Hameed ◽  
Emad Yousif ◽  
Mohammad Hayal Alotaibi ◽  
Dina S. Ahmed ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Surface Area ◽  
Pore Volume ◽  
High Surface ◽  
High Surface Area ◽  
Organic Polymers ◽  
Average Pore ◽  
Carbon Dioxide Uptake ◽  
Design And Synthesis ◽  
The One

The design and synthesis of new multifunctional organic porous polymers has attracted significant attention over the years due to their favorable properties, which make them suitable for carbon dioxide storage. In this study, 2-, 3-, and 4-hydroxybenzaldehyde reacted with phenyltrichlorosilane in the presence of a base, affording the corresponding organosilicons 1–3, which further reacted with benzidine in the presence of glacial acetic acid, yielding the organic polymers 4–6. The synthesized polymers exhibited microporous structures with a surface area of 8.174–18.012 m2 g−1, while their pore volume and total average pore diameter ranged from 0.015–0.035 cm3 g−1 and 1.947–1.952 nm, respectively. In addition, among the synthesized organic polymers, the one with the meta-arrangement structure 5 showed the highest carbon dioxide adsorption capacity at 323 K and 40 bar due to its relatively high surface area and pore volume.

Hypercrosslinked microporous polymers based on carbazole for gas storage and separation

RSC Advances ◽  
2014 ◽  
Vol 4 (105) ◽  
pp. 61051-61055 ◽  
Author(s):  
Xiao Yang ◽  
Miao Yu ◽  
Yang Zhao ◽  
Chong Zhang ◽  
Xiaoyan Wang ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Surface Area ◽  
Gas Storage ◽  
Carbazole Derivatives ◽  
Carbon Dioxide Uptake ◽  
Microporous Polymers

Hypercrosslinked microporous polymers from carbazole derivatives exhibit highly surface area of 1845 m2 g−1 and a carbon dioxide uptake ability of 4.63 mmol g−1 at 1.13 bar and 273 K.

Remarkable gas adsorption by carbonized nitrogen-rich hypercrosslinked porous organic polymers

2014 ◽  
Vol 2 (36) ◽  
pp. 15139-15145 ◽  
Author(s):  
Xiao Yang ◽  
Miao Yu ◽  
Yang Zhao ◽  
Chong Zhang ◽  
Xiaoyan Wang ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Surface Area ◽  
Gas Adsorption ◽  
High Surface ◽  
High Surface Area ◽  
Organic Polymer ◽  
High Carbon ◽  
Porous Organic Polymer ◽  
Carbon Dioxide Uptake ◽  
High Carbon Dioxide

Carbonized materials from a nitrogen-rich hypercrosslinked porous organic polymer exhibit a high surface area of 2065 m2 g−1 and an exceptionally high carbon dioxide uptake up to 6.51 mmol g−1 (1.13 bar/273 K).

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