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Graphical abstract Highlights • A facile method was developed to synthesize regenerable and H 2 O resistance sorbent for Hg0 removal. • The Ag nanoparticles were successively confined inside the mesoporous channels of MCM-41 molecule sieve. • The nanoconfinement effect is conducive to excellent Hg0 removal performance and regeneration ability. • The high hydrophobicity of Ag/MCM-41 is beneficial for the resistance to H 2 O. Abstract A facile passivation treatment and amino functionalized method was developed for controllable synthesis of effective and water-resistant Ag/MCM-41 composite sorbent for Hg0 removal in natural gas. The Ag nanoparticles were successively confined inside the mesoporous channels of MCM-41 molecule sieve with an average diameter of 3 nm. The synthesized sorbent was found to achieve a complete removal of Hg0 at high space velocity of 50,000 h−1 in ambient temperature. At 5% breakthrough, the Hg0 capture capacity of 1% (wt%) silver loaded Ag/MCM-41 was as high as 6.64 mg·g−1, which is much higher than the sample of Ag loaded outside of the pore channels (S-Ag/MCM-41) and other existing commercial sorbents. The H 2 O has negligible inhibitory effect on Hg0 removal performance of Ag/MCM-41. In addition, the spent Ag/MCM-41 could be easily regenerated without significant performance degradation over five cycles. We considered the high Hg0 capture efficiency, large adsorption capacity and excellent regeneration performance of Ag/MCM-41 are contributed to the nanoconfinement effect of mesoporous channels of MCM-41 molecule sieve which effectively prevented the growth and agglomeration of Ag nanoparticles. The good hydrophobicity of Ag/MCM-41 is beneficial for the high resistance to H 2 O. This work represents a giant step toward the preparation of effective sorbent for practical applications of Hg0 removal in natural gas. [ABSTRACT FROM AUTHOR]

A fixed-bed reactor was used to study the effect of water vapor on the efficiency of Hg 0 removal over CeO 2 -modified semi-coke. Adsorption experiments showed that the oxidation activity, and therefore, the mercury adsorption efficiency decreased with increasing water vapor concentrations. Hydrogen temperature-programmed reduction (H 2 -TPR) indicated that the oxidation activity of CeO 2 decreased after water vapor treatment. Fourier-transform infrared (FT-IR) studies revealed that CeO 2 -H 2 O showed new bending vibration peaks at 1110 cm −1 ascribed to Ce–OH groups. X-ray photoelectron spectroscopy (XPS) results showed that the content of Ce–OH increased from 20.85% to 39.99%, while the lattice oxygen content decreased from 68.21% to 45.83% after water vapor treatment. Density functional theory (DFT) calculations revealed that H 2 O can be dissociated on clean and oxygen-defective CeO 2 (1 1 1) surfaces to form H atoms and OH fragments. The H atoms associated with the adjacent oxygen atoms of CeO 2 , and the OH fragments were bound directly with Ce atoms to form Ce–OH for the clean CeO 2 surface; or occupied the oxygen vacancies and were surrounded by three Ce atoms via van der Waals forces, without additional bond formation for the oxygen-defective CeO 2 surface. Thus, the formation of Ce–OH groups and the consumption of lattice oxygens reduced the Hg 0 removal efficiency. [ABSTRACT FROM AUTHOR]