Graphene oxide/mixed metal oxide hybrid materials for enhanced adsorption desulfurization of liquid hydrocarbon fuels

被引:77
作者
Menzel, Robert [1 ,3 ]
Iruretagoyena, Diana [2 ]
Wang, Yifan [1 ]
Bawaked, Salem M. [4 ,5 ]
Mokhtar, Mohamed [4 ,5 ]
Al-Thabaiti, Shaeel A. [4 ,5 ]
Basahel, Sulaiman N. [4 ,5 ]
Shaffer, Milo S. P. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, England
[3] Bio Nano Consulting, Gridiron Bldg,One Pancras Sq, London N1C 4AG, England
[4] King Abdulaziz Univ, Fac Sci, Dept Chem, Jeddah, Saudi Arabia
[5] King Abdulaziz Univ, Surface Chem & Catalyt Studies Grp, Jeddah 21413, Saudi Arabia
基金
英国工程与自然科学研究理事会;
关键词
Graphene oxide; Mixed metal oxide; Dibenzothiophene; Adsorption; Desulfurization; LAYERED DOUBLE HYDROXIDE; DIBENZOTHIOPHENE; REMOVAL; SULFUR; DEEP; CHALLENGES; AEROGELS; DIESEL; LIGHT;
D O I
10.1016/j.fuel.2016.04.125
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
A series of mixed metal oxides (MMOs) adsorbents (MgAl-, CuAl-and CoAl-MMOs) were supported on graphene oxide (GO) through in-situ precipitation of layered double hydroxides (LDHs) onto exfoliated GO, followed by thermal conversion. The study shows that GO is an excellent support for the LDH-derived MMOs due to matching geometry and charge complementarity, resulting in a strong hybrid effect, evidenced by significantly enhanced adsorption performance for the commercially important removal of heavy thiophenic compounds from hydrocarbons. Fundamental liquid-phase adsorption characteristics of the MMO/GO hybrids are quantified in terms of adsorption equilibrium isotherms, selectivity and adsorbent regenerability. Upon incorporation of as little as 5 wt% GO into the MMO material, the organosulfur uptake was increased by up to 170%, the recycling stability was markedly improved and pronounced selectivity for thiophenic organosulfurs over sulfur-free aromatic hydrocarbons was observed. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:531 / 536
页数:6
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