2021
DOI: 10.1016/j.jhazmat.2020.124965
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A comparative study of the removal of o-xylene from gas streams using mesoporous silicas and their silica supported sulfuric acids

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Cited by 16 publications
(14 citation statements)
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“…Especially at 700 °C, the o -xylene breakthrough from the HIO bed remained unseen until 54 h, and the process curve was also different as compared to the curves acquired at lower temperatures ( Figure 2 b), thus, implying that HIO might have possessed super capacity (more than 691 mg g[Fe] −1 ) and unique reaction mechanism for removing o -xylene, which need to be studied further. Comparing Q B of HIO for removing o -xylene with other materials already reported in the literature [ 9 , 10 , 11 , 12 ], the value obtained here was higher.…”
Section: Resultssupporting
confidence: 40%
See 1 more Smart Citation
“…Especially at 700 °C, the o -xylene breakthrough from the HIO bed remained unseen until 54 h, and the process curve was also different as compared to the curves acquired at lower temperatures ( Figure 2 b), thus, implying that HIO might have possessed super capacity (more than 691 mg g[Fe] −1 ) and unique reaction mechanism for removing o -xylene, which need to be studied further. Comparing Q B of HIO for removing o -xylene with other materials already reported in the literature [ 9 , 10 , 11 , 12 ], the value obtained here was higher.…”
Section: Resultssupporting
confidence: 40%
“…Therefore, the development of new technologies to prevent the VOC contamination is currently of significant interest [ 5 , 6 , 7 , 8 ]. Among these, the processes that can enable the achievement of VOC resource utilization are a key to move towards sustainability; thus, these have received an increasing attention in recent years [ 9 , 10 , 11 , 12 , 13 , 14 ]. Considering that the mainstream technologies for VOCs elimination such as catalytic oxidation and thermal combustion are based on VOCs oxidation reactions, it is suspected that VOCs have a potential as reducing agents in the iron-making process from iron oxide ores.…”
Section: Introductionmentioning
confidence: 99%
“…However, as can be seen from Figure 1 and Table 1 (the TG curves and the calculated amount of the P-and C-state H 2 SO 4 for the SSA(E)-4 and SSA(W)-4), the proportion of the C-state H 2 SO 4 in SSA(E)-4 was higher than that in SSA(W)-4, indicating that the features of the solvents affected the anchoring states of sulfuric acid in SG support. As suggested in our previous studies [22,23], the C-state H 2 SO 4 , defined as the chemically bonded sulfuric acid, was formed by the condensation of silanol groups of SG surface and sulfuric acid molecules, and it was higher than the P-state counterpart (defined as the physisorbed sulfuric acid) in the bond strength. It was speculated that the use of ethyl acetate as the impregnation medium might promote the condensation of silanol groups and H 2 SO 4 molecules since it is a weakly polar solvent (dipole moment µ = 4.40, dielectric constant ε = 6.02) without hydroxyl groups compared with water (µ = 1.84, ε = 80.10) [24].…”
Section: Loading Amount and Anchoring States Of Sulfuric Acid In The ...mentioning
confidence: 61%
“…It is speculated that the observed adsorption superiority of SSA(E)-4 towards o-xylene was closely associated with a higher amount of the C-state H 2 SO 4 as compared to SSA(E)-4. Gao et al [23] suggested that the C-state sulfuric acid had higher thermal stability than the P-state counterpart, thereby leading to a superior performance in SSA(E)-4 for removing o-xylene from the gas stream.…”
Section: Effect Of Temperature On Adsorption Of Ssa(e)-4 and Ssa(w)-4...mentioning
confidence: 99%
“…The data obtained from this model can be used to calculate the theoretical breakthrough time (t B,th , min) and theoretical breakthrough adsorption capacity (Q B,th , mg g −1 ). The Equation (2) for this model is [37]:…”
Section: Model Of the Breakthrough Curvesmentioning
confidence: 99%