BACKGROUND OF THE INVENTION
1. Field of the Invention
[0001] The invention relates generally to the use of inorganic carbonates in the conversion
of biomass, and more specifically to the decomposition and regeneration of such inorganic
carbonates.
2. Description of the Related Art
[0002] Inorganic carbonates, in particular sodium carbonate and potassium carbonate, have
been proposed as catalysts for the conversion of biomass. It is also known that carbonates,
in particular potassium carbonate, are formed as a byproduct of the conversion of
certain types of biomass. However, the role of inorganic carbonates in biomass conversion
has been poorly understood, which has led to on the one hand a sub-optimal use of
these carbonates and, on the other hand, to an undesirable accumulation of carbonates
in biomass conversion reactors due to the formation of carbonates as a byproduct.
[0003] Thus, there is a particular need for an optimized process for the catalytic conversion
of solid biomass material making use of the catalytic properties of inorganic carbonates.
BRIEF SUMMARY OF THE INVENTION
[0004] The present invention addresses these problems by providing a process for the catalytic
conversion of solid biomass material, said process comprising the steps of:
- (i) reacting the solid biomass with an inorganic carbonate, whereby a bio-oil is formed
and at least part of the inorganic carbonate is converted to the corresponding hydroxide;
- (ii) regenerating the hydroxide to the corresponding carbonate; and
- (iii) recycling the carbonate obtained in step (ii) to step (i).
[0005] Another aspect of the invention comprises a method for recovering heat from char
and coke that are formed during the biomass conversion. Suitably, the step of regenerating
the hydroxide to the corresponding carbonate is combined with the step of recovering
heat from char and coke.
DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
[0006] The present invention is based on the discovery that inorganic carbonates decompose
to the corresponding metal oxide and carbon dioxide under conditions that are suitable
for their catalytic conversion of biomass material to a bio-oil.
[0007] This discovery has led to the development of a catalytic conversion process for solid
biomass material, said process comprising the steps of (i) reacting the solid biomass
with an inorganic carbonate whereby a bio-oil is formed and at least part of the inorganic
carbonate is converted to the corresponding hydroxide; (ii) regenerating the hydroxide
to the corresponding carbonate; and (iii) recycling the carbonate obtained in step
(ii) to step (i).
[0008] Schematically, this can be represented as follows:
XO.CO
2 + biomass → XOH + H
2O + CO
2 + activated biomass
XOH + activated biomass → bio-oil + H
2O + XO
XO + CO
2 → XO.CO
2
[0009] The temperature in step (i) is generally in the range of from 200°C to 500°C, more
preferably in the range of from 350°C to 450°C. These temperatures are normally not
considered high enough to cause the decomposition of inorganic carbonates. However,
due to interactions that exist between the carbonate and the biomass material, at
least partial decomposition of the organic carbonates occurs at these temperatures.
[0010] In addition, bio-oil that is formed in the conversion of biomass is highly acidic,
due to the presence of organic acids such as carboxylic acids. Typically, bio-oils
produced in these reactions have a pH of less than 3. This is low enough to convert
an inorganic carbonate to the corresponding hydrogen carbonate, or bicarbonate. The
bicarbonates are thermally considerably less stable than the carbonates from which
they derive.
[0011] In a sense, the reaction is self catalyzed. The formation of a small amount of a
bio-oil lowers the pH, thereby accelerating the decomposition of the carbonate. The
metal hydroxide resulting from the decomposition of the carbonate access a sink for
the acidic bio-oil compounds that are formed. The presence of the metal hydroxide
thereby facilitates the formation of the acidic bio-oil.
[0012] An important corollary to the above described reaction mechanism is the fact that
the inorganic carbonates are not true "catalysts" in that they are themselves converted
in the reaction that is catalyzed by them. As a consequence, they need to be converted
back to the original carbonate before they can be utilized again in the biomass conversion
reaction.
[0013] To some extent, regeneration of the hydroxide to the carbonate may take place
in situ, as sufficient CO
2 may be formed in the biomass conversion to react at least some of the hydroxide back
to the corresponding carbonate. This may be a reason why the need for regeneration
is not generally recognized by those active in this field.
[0014] The picture is complicated further by the fact that biomass material from most sources
contains considerable amounts of inorganic materials, which form a solid byproduct
generally referred to as "ash". Depending on the reaction conditions, at least part
of the ash will be in the form of inorganic carbonates.
[0015] As a result of these complicating factors, prior art processes tend to operate with
uncontrolled amounts of inorganic carbonates. On the one hand, unknown quantities
of carbonate are lost to conversion to the corresponding hydroxide. On the other hand,
equally unknown quantities of carbonate may be formed from the inorganic materials
present in the biomass feedstock.
[0016] The process of the present invention addresses the former issue by providing a regeneration
step in which hydroxide is converted to the corresponding carbonate. In a preferred
embodiment the process of the invention addresses the latter issue by recovering carbonates
present in the ash by-product and recycling them back into the process to the extent
required.
[0017] The process of the invention is suitable for conversion of any type of solid biomass
material to form a bio-oil. The process is particularly suitable for the conversion
of biomass comprising cellulose. The biomass feedstock used in the process may further
comprise lignin.
[0018] An important aspect of the process of invention is the formation of bio-oil. In addition,
part of the biomass is converted to non-condensable gases. During the conversion reaction
to a solid residue is formed as well. The solid residue may contain any unconverted
solid biomass material. The solid residue further comprises solid reaction products
of the biomass conversion reaction, in general coke and char. The inorganic materials
present in the biomass feedstock to some extent end up in the gas phase in the form
of fly ash; for the most part, however, the ash is present in the solid residue, generally
embedded in the char.
[0019] Any inorganic carbonate that was added to the reaction mixture will also find its
way to the solid residue of the biomass conversion reaction. For reasons explained
above, at least some of the inorganic carbonate may be present in the solid residue
in the form of the hydroxide.
[0020] It is desirable to bum the char and/or coke present in the solid residue by heating
the solid residue in an oxygen containing gas. A suitable example of an oxygen containing
gas is air. Heat generated by burning the char and/or coke can be used to supply heat
to the biomass conversion step. Significant amounts of CO
2 are formed during the burning of the char and coke. Any metal hydroxide or metal
oxide present in the solid residue is converted to the corresponding carbonate during
this regeneration step. A suitable regeneration temperature is in the range of from
550°C to 800°C, typically around 650°C.
[0021] Regenerated carbonate is recycled back into step (i). Suitably, the carbonate particles
may be used to carry heat from the regeneration reaction to the biomass conversion
step.
[0022] Any inorganic carbonate is suitable for use as a catalyst in step (i) of the process.
Particularly suitable are the carbonates of the monovalent and divalent metals. The
monovalent alkali metals are particularly preferred, especially sodium and potassium.
[0023] The ash formed in the solid residue of the biomass conversion reaction may comprise
the oxide, the hydroxide or the carbonate of alkali metals and earth alkaline metals.
The ash can be converted to the carbonate ash in step (ii), and the carbonate ash
can be recycled to step (i).
1. A process for the catalytic conversion of solid biomass material, said process comprising
the steps of:
(i) reacting the solid biomass with an inorganic carbonate, whereby a bio-oil is formed
and at least part of the inorganic carbonate is converted to the corresponding hydroxide;
(ii) regenerating the hydroxide to the corresponding carbonate; and
(iii) recycling the carbonate obtained in step (ii) to step (i).
2. The process of claim 1 wherein the solid biomass comprises cellulose.
3. The process of claim 2 wherein the solid biomass further comprises lignin.
4. The process of any one of the preceding claims whereby, in step (i), a solid residue
is formed.
5. The process of claim 4 wherein the solid residue comprises the hydroxide, and solid
reaction products of the biomass.
6. The process of claim 5 wherein the solid reaction products of the biomass comprise
char and ash.
7. The process of claim 6 wherein step (ii) comprises burning the char off the solid
residue in an oxygen-containing gas.
8. The process of any one of the preceding claims wherein the inorganic carbonate is
the carbonate of a monovalent or divalent metal.
9. The process of claim 8 wherein the monovalent metal or divalent metal is an alkali
metal or an earth alkaline metal.
10. The process of claim 9 wherein the inorganic carbonate is sodium carbonate, potassium
carbonate, or a mixture of sodium carbonate and potassium carbonate.
11. The process of claim 6 wherein the ash comprises the oxide, the hydroxide or the carbonate
of an alkali metal and/or an earth alkaline metal.
12. The process of claim 11 wherein the ash is converted to carbonate ash in step (ii),
and the carbonate ash is recycled to step (i).