Aqueous miscible organic-layered double hydroxides with improved CO2 adsorption capacity

Adsorption ◽  
2020 ◽  
Vol 26 (7) ◽  
pp. 1127-1135 ◽  
Author(s):  
Xuancan Zhu ◽  
Chunping Chen ◽  
Yixiang Shi ◽  
Dermot O’Hare ◽  
Ningsheng Cai
2012 ◽  
Vol 24 (23) ◽  
pp. 4531-4539 ◽  
Author(s):  
Ainara Garcia-Gallastegui ◽  
Diana Iruretagoyena ◽  
Veronica Gouvea ◽  
Mohamed Mokhtar ◽  
Abdullah M. Asiri ◽  
...  

Materials ◽  
2020 ◽  
Vol 13 (18) ◽  
pp. 4089
Author(s):  
Cristina Modrogan ◽  
Simona Cǎprǎrescu ◽  
Annette Madelene Dǎncilǎ ◽  
Oanamari Daniela Orbuleț ◽  
Eugeniu Vasile ◽  
...  

Magnesium–aluminum (Mg-Al) and magnesium–aluminum–nickel (Mg-Al-Ni) layered double hydroxides (LDHs) were synthesized by the co-precipitation method. The adsorption process of Mn2+ from synthetic wastewater was investigated. Formation of the layered double hydroxides and adsorption of Mn2+ on both Mg-Al and Mg-Ni-Al LDHs were observed by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy Dispersive Spectrometry (EDX) analysis. XRD patterns for prepared LDHs presented sharp and symmetrical peaks. SEM studies revealed that Mg-Al LDH and Mg-Al-Ni LDH exhibit a non-porous structure. EDX analysis showed that the prepared LDHs present uniformly spread elements. The adsorption equilibrium on these LDHs was investigated at different experimental conditions such as: Shaking time, initial Mn2+ concentration, and temperatures (10 and 20 °C). The parameters were controlled and optimized to remove the Mn2+ from synthetic wastewater. Adsorption isotherms of Mn2+ were fitted by Langmuir and Freundlich models. The obtained results indicated that the isotherm data fitted better into the Freundlich model than the Langmuir model. Adsorption capacity of Mn2+ gradually increased with temperature. The Langmuir constant (KL) value of Mg-Al LDH (0.9529 ± 0.007 L/mg) was higher than Mg-Al-Ni LDH (0.1819 ± 0.004 L/mg), at 20 °C. The final adsorption capacity was higher for Mg-Al LDH (91.85 ± 0.087%) in comparison with Mg-Al-Ni LDH (35.97 ± 0.093%), at 20 °C. It was found that the adsorption kinetics is best described by the pseudo-second-order model. The results indicated that LDHs can be considered as a potential material for adsorption of other metallic ions from wastewater.


2019 ◽  
Vol 19 (3) ◽  
pp. 475-483 ◽  
Author(s):  
Muvumbu Jean-Luc Mukaba ◽  
Alechine Emmanuel Ameh ◽  
Chuks Paul Eze ◽  
Leslie Felicia Petrik

Author(s):  
Joanna Srenscek-Nazzal ◽  
Urszula Narkiewicz ◽  
Antoni W. Morawski ◽  
Rafal J. Wróbel ◽  
Beata Michalkiewicz

2020 ◽  
Vol 294 ◽  
pp. 109871 ◽  
Author(s):  
Satriyo Krido Wahono ◽  
Joseph Stalin ◽  
Jonas Addai-Mensah ◽  
William Skinner ◽  
Ajayan Vinu ◽  
...  

Energies ◽  
2019 ◽  
Vol 12 (17) ◽  
pp. 3294 ◽  
Author(s):  
Zhenjian Liu ◽  
Zhenyu Zhang ◽  
Xiaoqian Liu ◽  
Tengfei Wu ◽  
Xidong Du

Carbon dioxide (CO2) has been used to replace coal seam gas for recovery enhancement and carbon sequestration. To better understand the alternations of coal seam in response to CO2 sequestration, the properties of four different coals before and after supercritical CO2 (ScCO2) exposure at 40 °C and 16 MPa were analyzed with Fourier Transform infrared spectroscopy (FTIR), low-pressure nitrogen, and CO2 adsorption methods. Further, high-pressure CO2 adsorption isotherms were performed at 40 °C using a gravimetric method. The results indicate that the density of functional groups and mineral matters on coal surface decreased after ScCO2 exposure, especially for low-rank coal. With ScCO2 exposure, only minimal changes in pore shape were observed for various rank coals. However, the micropore specific surface area (SSA) and pore volume increased while the values for mesopore decreased as determined by low-pressure N2 and CO2 adsorption. The combined effects of surface property and pore structure alterations lead to a higher CO2 adsorption capacity at lower pressures but lower CO2 adsorption capacity at higher pressures. Langmuir model fitting shows a decreasing trend in monolayer capacity after ScCO2 exposure, indicating an elimination of the adsorption sites. The results provide new insights for the long-term safety for the evaluation of CO2-enhanced coal seam gas recovery.


Processes ◽  
2019 ◽  
Vol 7 (9) ◽  
pp. 634 ◽  
Author(s):  
Shazia Shukrullah ◽  
Muhammad Yasin Naz ◽  
Norani M. Mohamed ◽  
Khalid A. Ibrahim ◽  
Nasser M. AbdEl-Salam ◽  
...  

Carbon dioxide is one of the major greenhouse gases and a leading source of global warming. Several adsorbent materials are being tested for removal of carbon dioxide (CO2) from the atmosphere. The use of multiwalled carbon nanotubes (MWCNTs) as a CO2 adsorbent material is a relatively new research avenue. In this study, Fe2O3/Al2O3 composite catalyst was used to synthesize MWCNTs by cracking ethylene gas molecules in a fluidized bed chemical vapor deposition (CVD) chamber. These nanotubes were treated with H2SO4/HNO3 solution and functionalized with 3-aminopropyl-triethoxysilane (APTS). Chemical modification of nanotubes removed the endcaps and introduced some functional groups along the sidewalls at defected sites. The functionalization of nanotubes with amine introduced carboxylic groups on the tube surface. These functional groups significantly enhance the surface wettability, hydrophilicity and CO2 adsorption capacity of MWCNTs. The CO2 adsorption capacity of as-grown and amine-functionalized CNTs was computed by generating their breakthrough curves. BELSORP-mini equipment was used to generate CO2 breakthrough curves. The oxidation and functionalization of MWCNTs revealed significant improvement in their adsorption capacity. The highest CO2 adsorption of 129 cm3/g was achieved with amine-functionalized MWCNTs among all the tested samples.


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