z-logo
Premium
Highly efficient methane reforming over a low‐loading Ru/γ‐Al 2 O 3 catalyst in a Pd‐Ag membrane reactor
Author(s) -
Simakov David S. A.,
RománLeshkov Yuriy
Publication year - 2018
Publication title -
aiche journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.958
H-Index - 167
eISSN - 1547-5905
pISSN - 0001-1541
DOI - 10.1002/aic.16094
Subject(s) - syngas , methane , catalysis , steam reforming , membrane reactor , chemistry , hydrogen , bar (unit) , catalytic reforming , methane reformer , carbon fibers , chemical engineering , nuclear chemistry , hydrogen production , materials science , organic chemistry , physics , meteorology , composite number , engineering , composite material
Natural gas can be reformed to syngas (CH 4  + H 2 O = CO + 3H 2 ), at temperatures above 850°C. Membrane catalytic reformers can provide high CH 4 conversions at temperatures below 650°C, by separating H 2 from the reactive mixture. Traditional Ni‐based catalysts suffer from low activity at low temperatures and deactivate rapidly by coking, particularly at low steam/carbon ratios. In this study, an ultralow loading (0.15 wt %) Ru/γ‐Al 2 O 3 catalyst was implemented in a lab‐scale membrane reformer, using a supported 5μm Pd‐Ag film membrane. Methane conversions above 90% were achieved at 650°C, 8 bar, and H 2 O/CH 4  = 2, 3 with contact times of ca. 10 s. The system generated up to 3.5 mol of ultrapure H 2 per mol of CH 4 fed, with a maximum power density of 0.9 kW/L. No significant deactivation was observed after 200 h time on stream, even when using low H 2 O:CH 4 ratios. © 2018 American Institute of Chemical Engineers AIChE J , 64: 3101–3108, 2018

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom