Chemistry Reference
In-Depth Information
Table 3 An overview of MTH process development.
Year
Developed by
Process
Statues
1981-1984 Mobil
MTG
Demonstrated on a 4 b/d plant in Paulsboro,
NJ, USA.
65
1981-1984 Mobil
MTG
Demonstrated on a 100 b/d plant in
Wesseling, Germany.
66
1985
Mobil
MTG
Commercialized in New Zealand
(14500 b/d).
59
TIGAS
b
1980s
Haldor Topsøe
A demonstration plant developed based on
ZSM-5 (1 t/d).
67
2009
Shanxi Coal Institute MTG
A demonstration plant brought on stream in
Shanxi, province, China (100 kt/y).
47
2009
UOP/INEOS and
Total OCP
a
MTO
A semi-commercial demonstration unit built
in Feluy, Belgium (10 t/d).
68
2010
CAC Chemnitz
STF
Currently in a demonstration phase
syngas-to-fuel unit, developed in
Germany.
69
2010
Haldor Topsøe
TIGAS
Currently being demonstrated in Des
Plaines, USA, where a wood gasifier is
running.
70
DMTO
c
2010
Dalian Institute for
Chemical Physics
A plant based on SAPO-34 started in Baotou,
China (600 kt/y).
47
2010
Lurgi
MTP
First plant started in China (500 kt/y propene
and 185 kt/y gasoline).
47
2011
UOP
Advanced
MTO
Construction of a plant in Nanjing, China
announced (295 kt/y).
47
2012
ExxonMobil
MTG
Announced a licensing agreement with
Sundrop Fuels Inc. (3,500 b/d).
71
2012
UOP
Advanced
MTO
Announced a licensing agreement with
China's Jiutai Energy (Zhungeer) Co. Ltd.
(600 kt/y).
72
2012
UOP
Advanced
MTO
Announced a licencing agreement
with Shandong Yangmei Hengtong
Chemicals Co. Ltd. (295 kt/y)
73
2013
UOP
Advanced
MTO
Announced a licensing agreement with
Jiangsu Sailboat Co. Ltd. (833 kt/y)
73
a
Olefin cracking process.
b
Topsøe integrated gasoline synthesis process.
c
Dalian methanol to olefins.
mechanistic works were devoted to direct formation of carbon-carbon
bonds from C
1
units (methanol or dimethyl ether), and several mech-
anisms were proposed.
47
However, high energy barriers are involved in
the direct coupling of C
1
units, and the proposed mechanisms lack ex-
perimental evidence.
47
Already in 1979, Chen and Reagan suggested that
the MTH reaction was autocatalytic.
74
20 years later, Song et al. per-
formed the MTH reaction using extremely purified reagents and reported
a dramatic decrease in the initial rate of methanol conversion.
75
It was
suggested from the observation that the rate at which the direct C
1
-C
1
coupling operates is irrelevant compared to the rate at which trace im-
purities of C
2
þ
compounds initiate the reaction. Recent theoretical work
also illuminate the main bottlenecks of C
1
-C
1
coupling reactions, and
support the conclusion that this route is not viable.
76
At present, the