Study of Solid Amine CO2 Sorbents Based on the Modified Fly Ash

2013 ◽  
Vol 448-453 ◽  
pp. 174-177
Author(s):  
Ying Lu Ji ◽  
Hui Ping Song ◽  
Fang Qin Cheng ◽  
Nan Zheng ◽  
Xu Ming Wang

In this paper, coal fly ash was modified by the hydrothermal synthesis method based on sodium hydroxide solution, and then was macerated by ethanol amine. Then we obtained the solid amine adsorbents used to absorb CO2. The modified fly ash was investigated by scanning electron microscope (SEM) and the specific surface area analyzer (BET) for the microstructure and specific surface area. Then, the solid CO2 adsorbent was analyzed by fourier transform infrared spectrometer (FT-IR) and thermal analyzer (TGA) in CO2 atmosphere. Results showed that modified fly ash generated many kinds of zeolite material by the SEM and the BET analysis, greatly increasing the specific surface area, improved the adsorption capacity. FT-IR analysis that the surface of solid amine CO2 adsorbent with amine groups; TGA analysis that compared with the original fly ash, CO2 adsorbent by this paper made has the capability of adsorption of CO2.

2011 ◽  
Vol 356-360 ◽  
pp. 1900-1908 ◽  
Author(s):  
Juliana De Carvalho Izidoro ◽  
Denise Alves Fungaro ◽  
Shao Bin Wang

A Brazilian fly ash sample (CM1) was used to synthesize zeolites by hydrothermal treatment. Products and raw materials were characterized in terms of real density (Helium Pycnometry), specific surface area (BET method), morphological analysis (SEM), chemical composition (XRF) and mineralogical composition (XRD). The zeolites (ZM1) from fly ash were used for metal ion removal from water. Results indicated that hydroxy-sodalite zeolite could be synthesized from fly ash sample. The zeolite presented higher specific surface area and lower SiO2/Al2O3ratio than the ash precursor. The adsorption showed that cadmium is more preferentially adsorbed on ZM1 than zinc. The adsorption equilibrium time for both Zn2+and Cd2+was 20 hours in a batch process. The adsorption isotherms were better fitted by the Langmuir model and the highest percentages of removal using ZM1 were obtained at pH 6 and 5 and doses of 15 and 18 g L-1for Zn2+and Cd2+, respectively. Thermodynamic studies indicated that adsorption of Zn2+and Cd2+by ZM1 was a spontaneous, endothermic process and presented an increase of disorder at the interface solid/solution.


Crystals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 178 ◽  
Author(s):  
Thye Foo Choo ◽  
Mohamad Amran Mohd Salleh ◽  
Kuan Ying Kok ◽  
Khamirul Amin Matori ◽  
Suraya Abdul Rashid

Mixture of aluminum dross (AD) and coal fly ash (CFA) was used to produce high-temperature porous mullite for washcoat application. CFA is the combustion by-product of pulverized coal in a coal-fired power plant, while AD is a waste product produced in secondary aluminum refining. In this study, 80 wt% of AD and 20 wt% of CFA was used to prepare a mullite precursor (MP) via acid leaching and dry-milling. The precursor was coated on a substrate and subsequently fired at 1500 °C. The results showed that the precursor transformed to a hierarchical porous microstructure assembled by large interlocked acicular mullite crystals. The pore structures consisted of large interconnected open pores and small pores. The specific surface area of the mullite washcoat was 4.85 m2g−1 after heating at 1500 °C for 4 h. The specific surface area was compatible with the specific surface area of other high-temperature washcoats.


2021 ◽  
Author(s):  
Prakash Parajuli ◽  
Sanjit Acharya ◽  
Julia Shamshina ◽  
Noureddine Abidi

Abstract In this study, alkali and alkaline earth metal chlorides with different cationic radii (LiCl, NaCl, and KCl, MgCl2, and CaCl2) were used to gain insight into the behavior of cellulose solutions in the presence of salts. The specific focus of the study was evaluation of the effect of salts’ addition on the sol-gel transition of the cellulose solutions and on their ability to form monoliths, as well as evaluation of the morphology (e.g., specific surface area, pore characteristics, and microstructure) of aerocelluloses prepared from these solutions. The effect of the salt addition on the sol-gel transition of cellulose solutions was studied using rheology, and morphology of resultant aerogels was evaluated by Scanning Electron Microscopy (SEM) and Brunauer-Emmett-Teller (BET) analysis, while the salt influence on the aerocelluloses’ crystalline structure and thermal stability was evaluated using powder X-Ray Diffraction (pXRD) and Thermogravimetric Analysis (TGA), respectively. The study revealed that the effect of salts’ addition was dependent on the component ions and their concentration. The addition of salts in the amount below certain concentration limit significantly improved the ability of the cellulose solutions to form monoliths and reduced the sol-gel transition time. Salts of lower cationic radii had a greater effect on gelation. However, excessive amount of salts resulted in the formation of fragile monoliths or no formation of gels at all. Analysis of surface morphology demonstrated that the addition of salts resulted in a significant increase in porosity and specific surface area, with salts of lower cationic radii leading to aerogels with much larger (~1.5 and 1.6-fold for LiCl and MgCl2, respectively) specific surface area compared to aerocelluloses prepared with no added salt. Thus, by adding the appropriate salt into the cellulose solution prior to gelation, the properties of aerocelluloses that control material’s performance (specific surface area, density, and porosity) could be tailored for a specific application.


Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1052 ◽  
Author(s):  
Juvet Malonda Shabani ◽  
Omotola Babajide ◽  
Oluwaseun Oyekola ◽  
Leslie Petrik

Zeolites are aluminosilicate crystalline materials known for their unique characteristics, and have been prominent for nearly half a century due to their wide and important industrial applications. The production of zeolites, however, remains a challenge due to the high cost of commercial reagents conventionally used as feedstocks. In the current study, hydroxy sodalite (HS) zeolite samples were synthesised from coal fly ash feedstock by a direct hydrothermal synthesis method. The effects of hydrothermal crystallisation synthesis time on phase crystallinity, crystal size, and morphology of the formed HS were investigated. The prepared samples were characterised using XRD, SEM, EDS and FT-IR techniques. The XRD results of the samples prepared with varying synthesis times confirmed the formation of HS from low to high phase purity and crystallinity from 11 to over 98%. The SEM results reflected gradual variation in crystal morphology, of which highly crystalline HS samples were associated with hexagonal-cubic and cubic-platelet crystals. The FTIR, depicting zeolite characteristics of T–O and T–O–T stretching vibrations in the molecular framework, further confirmed the formation of HS zeolites for samples obtained above the 24-h synthesis time. These zeolite samples were then evaluated for their catalytic activities in the conversion of maggot oil to biodiesel. The application of the various hydroxy sodalite samples for the transesterification of maggot oil yielded up to 84.10% biodiesel (FAME) with physicochemical properties that were in compliance with the biodiesel specification standards. This study investigated the novel use of a coal fly ash-derived, heterogeneous HS catalyst in biodiesel production from maggot oil, and indicates its potential to enhance biodiesel yield and quality upon process optimisation tests.


Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2424 ◽  
Author(s):  
Bao-guo Fan ◽  
Li Jia ◽  
Yan-lin Wang ◽  
Rui Zhao ◽  
Xue-song Mei ◽  
...  

In order to obtain the adsorption mechanism and failure characteristics of CO2 adsorption by potassium-based adsorbents with different supports, five types of supports (circulating fluidized bed boiler fly ash, pulverized coal boiler fly ash, activated carbon, molecular sieve, and alumina) and three kinds of adsorbents under the modified conditions of K2CO3 theoretical loading (10%, 30%, and 50%) were studied. The effect of the reaction temperature (50 °C, 60 °C, 70 °C, 80 °C, and 90 °C) and CO2 concentration (5%, 7.5%, 10%, 12.5%, and 15%) on the adsorption of CO2 by the adsorbent after loading and the effect of flue gas composition on the failure characteristics of adsorbents were obtained. At the same time, the microscopic characteristics of the adsorbents before and after loading and the reaction were studied by using a specific surface area and porosity analyzer as well as a scanning electron microscope and X-ray diffractometer. Combining its reaction and adsorption kinetics process, the mechanism of influence was explored. The results show that the optimal theoretical loading of the five adsorbents is 30% and the reaction temperature of 70 °C and the concentration of 12.5% CO2 are the best reaction conditions. The actual loading and CO2 adsorption performance of the K2CO3/AC adsorbent are the best while the K2CO3/Al2O3 adsorbent is the worst. During the carbonation reaction of the adsorbent, the cumulative pore volume plays a more important role in the adsorption process than the specific surface area. As the reaction temperature increases, the internal diffusion resistance increases remarkably. K2CO3/AC has the lowest activation energy and the carbonation reaction is the easiest to carry out. SO2 and HCl react with K2CO3 to produce new substances, which leads to the gradual failure of the adsorbents and K2CO3/AC has the best cycle failure performance.


2019 ◽  
Vol 26 (1) ◽  
pp. 99-102
Author(s):  
Dāvis CONKA ◽  
Līga AVOTINA ◽  
Ruta SVINKA ◽  
Visvaldis SVINKA ◽  
Laris BAUMANE ◽  
...  

Natural clay is a perspective material for application as sorbents for wastewater treatment as well as for sorption of radionuclides, where the properties of the clays can be changed under influence of ionizing radiation. For application of Latvian illite/kaolinite clays for isotope sorption it is important to characterize the physic-chemical properties of pre-prepared air dried clays. Two fractions of the illite clays were selected. A fraction with grain size 100 μm (SiO2 content 60.9 ± 1.5 wt.%, specific surface area 35 m2/g) and a sand free fraction – 2 μm (SiO2 47.7 ± 1.9 wt.%, specific surface area 38 m2/g). Selected fractions were irradiated with accelerated electrons (5 MeV, ELU-4, Salaspils, absorbed dose up to 500 kGy). Non-irradiated and irradiated clays were analysed with means of Fourier transform infrared (FT-IR) spectrometry.  


Clay Minerals ◽  
2018 ◽  
Vol 53 (4) ◽  
pp. 665-674 ◽  
Author(s):  
Emmanuel Ajenifuja ◽  
Abimbola P.I. Popoola ◽  
Kabir O. Oyedotun ◽  
Olawale Popoola

ABSTRACTKaolin and diatomite are abundant and widely available geological materials that may immobilize or stabilize functional chemical species on their surfaces for various applications. Acid-treated kaolin and diatomite were intercalated with photocatalyst Ag-TiO2nanoparticles using the sol–gel technique to prepare nanocomposite ceramic materials. The nanocomposites were sintered between 900°C and 1000°C to induce thermal reactions and to enhance nanoparticle–substrate attachment. Chemical and thermal characterizations of the acid-treated materials and intercalated nanocomposites were performed with energy-dispersive X-ray (EDX) analysis and differential scanning calorimetry (DSC), respectively. The Brunauer–Emmett–Teller (BET)-specific surface area and scanning electron microscopy (SEM) were employed for physical and microstructural characterization of the nanocomposites, respectively. Morphological studies revealed a uniform distribution of Ag-TiO2nanocrystallites in pores and on mineral particle surfaces. The BET analysis showed remarkable surface and grain modification by sintering. Decreases in the BET-specific surface area were observed for the sintered ceramic nanocomposite, Ag-TiO2-kaolin (20.244 to 5.446 m2/g) and Ag-TiO2-diatomite (19.582 to 10.148 m2/g).


NANO ◽  
2016 ◽  
Vol 11 (05) ◽  
pp. 1650052 ◽  
Author(s):  
Ying Chen ◽  
Shenglun Ji ◽  
Tengfei Qiao ◽  
Shuang Miao ◽  
Yu Zhao

Graphene–Bi2WO6 composite photocatalyst with excellent photocatalytic properties were synthetized by ultrasonic-microwave synergistic method. The obtained samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier infrared (FT-IR) spectrum, specific surface area analyzer (BET) and UV-Vis diffuse reflectance spectra. The photocatalytic activities of as-prepared samples were evaluated by degradation of pyridine in light oil under visible light irradiation. The results show that graphene changed appearance structure of Bi2WO6, which prevented the Bi2WO6 nanosheets reunion arrangement, and increased specific surface area of the catalyst. It can also reduce the recombination probability of photogenerated carrier, so as to improve the photocatalytic activity of the composite catalyst. The optimal amount of graphene is 2%, with the denitrification rate as high as 89.28%, much higher than that of pure Bi2WO6.


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