ZnO-CuO supported on activated carbon for H2S removal at room temperature

被引:127
作者
Balsamo, M. [1 ]
Cimino, S. [2 ]
de Falco, G. [2 ]
Erto, A. [1 ]
Lisi, L. [2 ]
机构
[1] Univ Naples Federico II, Dipartimento Ingn Chim Mat & Prod Ind, Ple Tecchio 80, I-80125 Naples, Italy
[2] CNR, IRC, Ple Tecchio 80, I-80125 Naples, Italy
关键词
Reactive adsorption; Mixed metal oxides; Sulphur poisoning; Sorbent; Gas cleaning; HYDROGEN-SULFIDE REMOVAL; ZINC-OXIDE SORBENTS; REACTIVE ADSORPTION; SURFACE-CHEMISTRY; GAS STREAMS; DESULFURIZATION; MECHANISM; DECOMPOSITION; NANOPARTICLES; PERFORMANCE;
D O I
10.1016/j.cej.2016.06.085
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
Sorbents for low temperature reactive adsorption of H2S were prepared by dispersing mixed Zn and Cu oxides onto a commercial activated carbon at fixed total metal loading and Cu:Zn atomic ratios from 0:1 to 1:1. Fresh and spent sorbents were characterized by means of ICP-MS, SEM-EDX, XRD, BET and pore size distribution, DRIFT and sulphur elemental analysis. H2S (50-3000 ppmv in N-2) removal tests were run under dynamic conditions at 30 degrees C. Due to the high dispersion of the metal oxide phase and its favorable interaction with the carbonaceous support, the functionalized sorbents showed a strongly enhanced adsorption capacity with respect to the raw activated carbon, under dry conditions. Furthermore, the utilization factor of the active phase (moles of S captured per mole of Cu + Zn) increased along with the Cu content up to 76%, thus demonstrating a clear promoting effect of Cu-insertion on the reactivity of ZnO, already at low Cu concentration. Temperature Programmed Desorption (TPD) of H2S and SO2 from saturated sorbents showed that H2S.adsorption was coupled with oxidation phenomena leading to the formation of metal sulphates apart from metal sulphides and/or elemental sulphur, testifying the complexity of the surface reactions. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:399 / 407
页数:9
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