Competitive Adsorption in a Multicomponent Diesel System Using Nickel Oxide/Activated Carbon

被引:0
作者
Nkomzwayo, Thulisile [1 ,2 ]
Mguni, Liberty L. [1 ]
Liu, Xinying [1 ]
Liu, Ran [1 ,3 ]
Yao, Yali [1 ]
机构
[1] Univ South Africa, Inst Dev Energy African Sustainabil IDEAS, ZA-1710 Roodepoort, South Africa
[2] Council Sci & Ind Res CSIR, ZA-0001 Brummeria, South Africa
[3] Hebei Univ Sci & Technol, Coll Chem & Pharmaceut Engn, Shijiazhuang 050018, Peoples R China
基金
新加坡国家研究基金会;
关键词
ACTIVATED CARBON; DEEP DESULFURIZATION; SELECTIVE ADSORPTION; FUEL; BENZOTHIOPHENE; NANOPARTICLES; ADSORBENT; GASOLINE; REMOVAL; SULFUR;
D O I
10.1021/acs.iecr.2c03745
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Nickel oxide, which acts as an intermediate Lewis acid, was loaded onto activated carbon (AC) to enhance the adsorption selectivity of AC in the desulfurization of model diesel. The total sulfur adsorption capacity increased from 2.46 to 4.42 mg-S center dot g adsorbent-1 and the total sulfur removal increased from 46.8 to 84.5% using the AC and Ni(10%)O/ AC adsorbents, respectively. Multicomponent isothermal modeling showed that the incorporation of NiO onto AC significantly improved the synergistic interactions between the thiophenic compounds while mitigating competitive interactions between the more steric 4,6-dimethyl dibenzothiophene (4,6-DMDBT) and 4-methyl-dibenzothiophene (4-MDBT) compounds. The mitigation was attributed to new adsorbate-specific sites created by loading NiO on AC. Spent adsorbent characterization and pyridine adsorption-IR analysis suggested that higher desulfurization performance of the Ni(10%)O/AC adsorbent was attributed to an increase in the adsorbent's Lewis acidity upon loading with NiO, leading to increased Ni-S acid-base interactions, in addition to pi-complexation.
引用
收藏
页码:3812 / 3827
页数:16
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