TY - JOUR
T1 - Micro-syngas technology options for GtL
AU - Trevisanut, Cristian
AU - Jazayeri, Seyed M.
AU - Bonkane, Said
AU - Neagoe, Cristian
AU - Mohamadalizadeh, Ali
AU - Boffito, Daria C.
AU - Bianchi, Claudia L.
AU - Pirola, Carlo
AU - Visconti, Carlo Giorgio
AU - Lietti, Luca
AU - Abatzoglou, Nicolas
AU - Frost, Lyman
AU - Lerou, Jan
AU - Green, William
AU - Patience, Gregory S.
N1 - Publisher Copyright:
© 2016 Canadian Society for Chemical Engineering.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Natural gas emissions contribute to climate change, and equally importantly, affect the health of populations near gas fields.[1] At night, the flares from the Bakken fields in North Dakota burn as bright as the lights in cities as large as Minneapolis. Rather than flaring (or worse, venting), this associated natural gas represents a multi-billion dollar opportunity.[2] Pipelines and liquefying natural gas are cost prohibitive in many cases. Converting methane to fuels is an attractive alternative. We examined three options to convert natural gas to syngas (H2 and CO), which is the first step to producing fuels: Steam Methane Reforming (SMR), Auto-Thermal Reforming (ATR), and Catalytic Partial Oxidation (CPOX). Based on a multi-objective optimization analysis, C5+ hydrocarbon yields are highest with CPOX as the first step followed by Fischer-Tropsch synthesis (FT). A micro-refinery with the CPOX-FT process treating 2800kL·d-1 (100 MCF·d-1) natural gas, produces 1300 L·d-1 (8.2 bbl·d-1) of C5+ hydrocarbons. Maximum yields for the SMR-FT and ATR-FT processes are 938 L·d-1 and 1100 L·d-1 (5.9 bbl·d-1, 7.0 bbl·d-1) of C5+, respectively. Large-scale POX and ATR processes produce 1600 L per 2800 kL (10 bbl per 100 MCF) of natural gas.
AB - Natural gas emissions contribute to climate change, and equally importantly, affect the health of populations near gas fields.[1] At night, the flares from the Bakken fields in North Dakota burn as bright as the lights in cities as large as Minneapolis. Rather than flaring (or worse, venting), this associated natural gas represents a multi-billion dollar opportunity.[2] Pipelines and liquefying natural gas are cost prohibitive in many cases. Converting methane to fuels is an attractive alternative. We examined three options to convert natural gas to syngas (H2 and CO), which is the first step to producing fuels: Steam Methane Reforming (SMR), Auto-Thermal Reforming (ATR), and Catalytic Partial Oxidation (CPOX). Based on a multi-objective optimization analysis, C5+ hydrocarbon yields are highest with CPOX as the first step followed by Fischer-Tropsch synthesis (FT). A micro-refinery with the CPOX-FT process treating 2800kL·d-1 (100 MCF·d-1) natural gas, produces 1300 L·d-1 (8.2 bbl·d-1) of C5+ hydrocarbons. Maximum yields for the SMR-FT and ATR-FT processes are 938 L·d-1 and 1100 L·d-1 (5.9 bbl·d-1, 7.0 bbl·d-1) of C5+, respectively. Large-scale POX and ATR processes produce 1600 L per 2800 kL (10 bbl per 100 MCF) of natural gas.
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U2 - 10.1002/cjce.22433
DO - 10.1002/cjce.22433
M3 - Article
AN - SCOPUS:84960089154
SN - 0008-4034
VL - 94
SP - 613
EP - 622
JO - Canadian Journal of Chemical Engineering
JF - Canadian Journal of Chemical Engineering
IS - 4
ER -