Biomass to Liquids (BtL)
Introduction
The term BtL is applied to synthetic fuels made from biomass through a thermo chemical route. The objective is to produce fuel components that are similar to those of current fossil-derived petrol (gasoline) and diesel fuels and hence can be used in existing fuel distribution systems and with standard engines. They are also known as synfuels.
Although the processes for production of BtL are well known and have been applied using fossil-feedstocks, such as methane (GtL) or coal, commercial biofuels based on these technolgies are not currently available in the market place.
However, BtL RD&D in Europe is gathering momentum, and the world's first commercial BtL Plant is under construction in Frieberg Saxony, utilising the Choren Carbo-V ® Process.
The Choren Carbo-V ® Process
© Copyright Choren
The Choren Carbo-V ® Process View
at larger size>>
The Carbo-V® Process is a three-stage gasification process resulting in the production of syngas:
- low temperature gasification,
- high temperature gasification and
- endothermic entrained bed gasification.
The Fischer-Tropsch (FT) process is then used to convert the synthesis gas into an automotive fuel SunDiesel®. The waxes formed during the FT synthesis are further processed using hydrocracking.
© Copyright Choren
Reactor being delivered to the Choren
BTL plant.
View
at larger size>>
The Choren website lists a number of advantages for SunDiesel®:
- High cetane number and therefore much better ignition performance than conventional diesel fuel,
- No aromatics or sulfur and significantly reduces pollutants from exhaust emissions,
- Can be used without any adjustment to existing infrastructure or engine systems,
- Largely CO2-neutral.
© Copyright Choren
SunDiesel® demonstration
fuel station at Choren BtL plant
View
at larger size>>
Presentation on Choren BtL plant from EBTP SPM2
CEA Bure Saudron Pilot Plant
In December 2009, CEA (Atomic and Alternative Energy Commission) France announced the construction of a pilot BTL plant in Bure Saudron. The plant will use 75000 tonnes per foresty and agricultural residues to produce ~23000 tonnes/year of biofuel (diesel, kerosene and naptha). The Bure Saudron project will add hydrogen during the synthesis stage to optimise the ratio with carbon monoxide [Source CEA].
NSE Biofuels Demonstration Plant
NSE Biofuels Oy - a joint venture between Neste Oil and Stora Enso - is building a BtL demonstration plant at Stora Enso’s Varkaus Mill in Finland, due to open in 2009. As well as providing test data and operating experience, the plant will also reduce greenhouse gas emissions as wood-based gas from the plant will replace oil in the pulp mill’s lime kiln, making the Varkaus integrate virtually fossil fuel free. Following trials, the joint venture will assess the viability of building a commercial production plant at one of Stora Enso’s mills.
Presentation on the Neste Oil Stora Enso joint venture from EBTP SMP2
© Copyright Stora
Enso
The NSE Biofuels BtL demonstration
plant.
The Dutch Biorefinery Initiative (DBI)
In 2009, a demonstration facility will be initiated in the Port of Rotterdam by WUR and ECN with support from the Netherlands government. This will include a 10 MWth entrained-flow gasification based syngas production platform for heat and power, base chemicals and BtL. Information on this project is included in the IEA Bioenergy Task 42 publication on Biorefineries
BtL Facts and Figures
BtL fuels may be produced from almost any type of low-moisture
biomass, residues or organic wastes such as short rotation trees, perennial
grasses, straw, forest thinnings, bark from paper-pulp production, bagasse,
waste paper or reclaimed wood or fibre based-composites.
It is estimated that over 4m3 of BtL-fuels can be produced per
hectare of land per annum. Hence, in future if 4-6 million hectares of land
were used to grow energy crops, one could replace 20-25 % of the liquid transport
fuel currently used.
The advantage of the BtL route to liquid transport fuels lies in the ability to use almost any type of biomass, with little pre-treatment other than moisture control. This is because the feedstock is gasified in the first stage of the process. The gas produced is then treated further to clean it, remove tars, particulates and gaseous contaminants, and to adjust the ratio of the required gases (hydrogen and carbon monoxide) to that required. The result is a balanced syngas that can be used in the second, catalytic, stage. Syngas may also be obtained by pyrolysis to form charcoal. The hot charcoal is then reacted with steam to produce watergas.
The two main catalytic processes for BtL production are Fisher-Tropsch and the Mobil Process
Fisher-Tropsch
The Fischer-Tropsch process is a catalyzed chemical reaction in which carbon monoxide and hydrogen are converted into liquid hydrocarbons of various forms. Generally the catalysts used, for the following reaction, are based on iron and cobalt.
(2n+1)H2 + n(CO) -> CnH2n+2 + nH2O
The FT process is an established technology and is already applied on a large scale from coal or natural gas. Developed in the 1920s in Germany, it was used by both Germany and Japan during World War II and later by South Africa and to a lesser extent in the United States.
One problem is the high capital cost of the multistage process. This may be greater when biomass is used as feedstock, since the scale of operation may be limited by the distance over which biomass can be transported to the factory at an economic price. Hence, the economy of scale is decreased compared to a large coal or gas-based operation. Running and maintenance costs are also comparatively high.
Mobil Process
This is a two stage catalytic process. In the first stage LINK
methanol is produced. The methanol is then used as feedstock to generate
hydrocarbons of varying chain length, using a zeolite catalyst. In the conversion,
a number of reactions take place in the gas phase. The conversion is initiated
by the removal of water to produce dimethyl ether:
2CH3OH(g) -> CH3OCH3(g) + H2O(g)
This is followed by various other reactions in which further molecules of
water are removed resulting in gradual increase in chain length.
These reactions
include the following.
2CH3OCH3(g) + 2CH3OH(g) -> C6H12(g) + 4H2O(g)
3CH3OCH3(g) -> C6H12(g) + 3H2O(g)
As a result of other dehydration reactions occuring in parallel a mixture
of hydrocarons is produced of which about 80% is suitable for petrol production.
The mixture contains (w/w) around 50% highly branched alkanes, 12% highly
branched alkenes, 7% cycloalkanes and 30% aromatics. This process has been
commercialised by Methanex in New Zealand using methanol produced from natural
gas.

