WO2001017643A1 - Apparatus and method for removing solvent residues - Google Patents

Apparatus and method for removing solvent residues Download PDF

Info

Publication number
WO2001017643A1
WO2001017643A1 PCT/GB2000/003319 GB0003319W WO0117643A1 WO 2001017643 A1 WO2001017643 A1 WO 2001017643A1 GB 0003319 W GB0003319 W GB 0003319W WO 0117643 A1 WO0117643 A1 WO 0117643A1
Authority
WO
WIPO (PCT)
Prior art keywords
steam
solvent
biomass
separator
vessel
Prior art date
Application number
PCT/GB2000/003319
Other languages
French (fr)
Inventor
Stuart Corr
Robert Elliott Low
James David Morrison
Frederick Thomas Murphy
Paul Alan Dowdle
Original Assignee
Ineos Fluor Holdings Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ineos Fluor Holdings Limited filed Critical Ineos Fluor Holdings Limited
Priority to MXPA02002431A priority Critical patent/MXPA02002431A/en
Priority to CA002383588A priority patent/CA2383588A1/en
Priority to AT00956674T priority patent/ATE273736T1/en
Priority to AU68545/00A priority patent/AU766475C/en
Priority to BR0013803-7A priority patent/BR0013803A/en
Priority to JP2001521425A priority patent/JP2003508205A/en
Priority to IL14843700A priority patent/IL148437A0/en
Priority to DE60013146T priority patent/DE60013146T2/en
Priority to EP00956674A priority patent/EP1212127B1/en
Priority to KR1020027002980A priority patent/KR20020042825A/en
Publication of WO2001017643A1 publication Critical patent/WO2001017643A1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D3/00Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D5/00Condensation of vapours; Recovering volatile solvents by condensation
    • B01D5/0033Other features
    • B01D5/0039Recuperation of heat, e.g. use of heat pump(s), compression
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D11/00Solvent extraction
    • B01D11/02Solvent extraction of solids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D11/00Solvent extraction
    • B01D11/02Solvent extraction of solids
    • B01D11/0215Solid material in other stationary receptacles
    • B01D11/0219Fixed bed of solid material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D11/00Solvent extraction
    • B01D11/02Solvent extraction of solids
    • B01D11/028Flow sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D3/00Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • B01D3/007Energy recuperation; Heat pumps
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D3/00Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • B01D3/34Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping with one or more auxiliary substances
    • B01D3/40Extractive distillation

Definitions

  • Biomass extraction is the extraction of flavours, fragrances or pharmaceutically active ingredients from materials of natural origin (these materials being referred to as “biomass”.
  • biomass materials include but are not limited to flavoursome or aromatic substances such as coriander, cloves, star anise, coffee, orange juice, fennel seeds, cumin, ginger and other kinds of bark, leaves, flowers, fruit, roots, rhizomes and seeds.
  • Biomass may also be extracted in the form of biologically active substances such as pesticides and pharmaceutically active substances or precursors thereto, obtainable e.g. from plant material, a cell culture or a fermentation broth.
  • solvents include liquefied carbon dioxide or, of particular interest, a family of solvents based on organic hydrofluorocarbon (“HFC”) species.
  • HFC organic hydrofluorocarbon
  • hydrofluorocarbon we are referring to materials which contain carbon, hydrogen and fluorine atoms only and which are thus chlorine-free.
  • Preferred hydrofluorocarbons are the hydrofluoroalkanes and particularly the Ci- 4 hydrofluoroalkanes.
  • Suitable examples of C ⁇ -4 hydrofluoroalkanes which may be used as solvents include, inter alia, trifluoromethane (R-23), fluoromethane (R-41), difluoromethane (R-32), pentafluoroefhane (R-125), 1 ,1,1- trifluoroethane (R-143a), 1,1,2,2-tetrafluoroethane (R-134), 1,1,1,2- tetrafluoroethane (R-134a), 1,1-difluoroethane (R-152a), heptafluoropropanes and particularly 1,1,1,2,3,3,3-heptafluoropropane (R-227ea), 1,1,1,2,3,3- hexafluoropropane (R-236ea), 1,1,1,2,2,3-hexa
  • R-134a, R-227ea, R-32, R-125, R-245ca and R-245fa are preferred.
  • An especially preferred hydrofluorocarbon for use in the present invention is 1,1,1 ,2-tetrafluoroethane (R- 134a) .
  • CFC's chlorofluorocarbons
  • HCFC's hydrochlorofluorocarbons
  • liquefied solvent is allowed to percolate by gravity in downflow through a bed of biomass held in vessel 11. Thence it flows to evaporator 12 where the volatile solvent is vaporised by heat exchange with a hot fluid. The vapour from evaporator 12 is then compressed by compressor 13. The compressed vapour is next fed to a condenser 14 where it is liquefied by heat exchange with a cold fluid. The liquefied solvent is then optionally collected in intermediate storage vessel 15 or returned (line 16) directly to the extraction vessel 1 to complete the circuit.
  • the biomass is usually chopped or ground in some manner in order to increase the surface area in contact with the extraction solvent. Whilst beneficially increasing the rate of extraction of the desired components during biomass extraction, this increased surface area acts to increase the quantity of solvent that can remain adsorbed onto and in the biomass after extraction. Clearly some cost-effective method of achieving acceptable residual HFC solvent levels in the exhausted biomass would be of significant value in the development of the technology.
  • a combination of evacuation and heat may act to reduce the levels of residual solvent in the biomass over a period of time.
  • This method however has a number of potential disadvantages including:
  • steam advantageously strips solvent (that typically is an HFC such as 1,1,1,2- tetrafluoroethane, or mixtures of HFC's) from the biomass.
  • solvent that typically is an HFC such as 1,1,1,2- tetrafluoroethane, or mixtures of HFC's
  • the solvent is then entrained in the steam and conveyed to the separator, where the steam and the solvent are separated to allow recovery and/or disposal of the solvent.
  • the steam may contact the biomass once; or the apparatus may optionally include means such as pipework and valves permitting the steam to contact the biomass more than once.
  • the source of steam supplies steam at or near atmospheric pressure.
  • the source of steam supplies steam at super-atmospheric pressure.
  • the separator is or includes an adsorbent material for removing solvent entrained with the steam. More preferably the adsorbent material is or includes activated carbon. These features conveniently make the solvent available for recycling, or permit ready disposal of the solvent.
  • the adsorbent filter material may also act to reduce any volatilised organic materials present in the depleted biomass, again improving the quality of the effluent condensate.
  • a concentrated stream of recovered HFC may be obtained from thermal regeneration of the adsorbent.
  • the loaded adsorbent provides a convenient, compact and cost-effective package for appropriate disposal.
  • Claims 7 and 8 define optional forms of apparatus of the invention, that include a condenser either upstream or downstream of the separator, to condense the stream and facilitate separation of the steam and solvent from one another.
  • Claim 8 defines a preferred form of extractor vessel.
  • the purpose of the optional connection to a vacuum or to suction is to permit evacuation of the vessel at the end of a biomass extraction, thereby removing from the vessel the bulk of the solvent therein. This means that the steam serves primarily to strip solvent that is adsorbed onto the surface of the biomass.
  • the vacuum connection may also advantageously be used to purge the vessel of e.g. water, when it is required to extract a new bed of biomass.
  • the extraction vessel is in use vertical, with the inlet at its lower end and the outlet at its upper end.
  • This advantageously allows the charging of the extraction vessel with a packed bed of biomass.
  • Such a packed bed may advantageously occupy substantially the entire cross-section of part of the vessel.
  • the extraction vessel may optionally include a selectively operable condenser (cooling) jacket. This allows steam condensing advantageously to occur within the extraction vessel.
  • the extraction vessel includes thermal insulation. This advantageously reduces heat transfer from the vessel during both the biomass extraction and desorption (solvent recovery) processes.
  • the method of the invention is superior to simple heating and/or evacuation, because
  • steam flow acts to maintain a low partial pressure of HFC solvent in the vapour space around the biomass thus aiding transfer of HFC from the biomass to the steam stream • water from the steam is likely to act to displace HFC from the surface of the biomass through preferential adsorption thus further improving the rate and effectiveness of desorption relative to a flow of other gases such as nitrogen.
  • Figure 1 is a schematic representation of a prior art closed loop biomass extraction circuit
  • Figure 2 is a schematic representation of apparatus according to the invention, that may be included in the Figure 1 circuit.
  • FIG. 2 there is shown a part of the Figure 1 circuit, modified in accordance with the invention.
  • the remainder of the circuit part-illustrated in Figure 2 is as shown in Figure 1.
  • FIG 2 shows the extraction vessel 11 of the Figure 1 apparatus, in the form of a hollow cylinder, closed at each end 11a, lib and being in the preferred embodiment of flanged tube construction.
  • vessel 11 is vertical as shown, although other orientations, e.g. inclined or horizontal, are possible.
  • a packed bed 12 of biomass is in use of the apparatus supported within extraction vessel 11, the cross-section of the packed bed 12 being substantially the same as that of the entire cross-section of the vessel 11 over a substantial part of its length.
  • the vessel 11 is used for biomass extraction, during which solvent such as an HFC is fed into the bottom 11a of vessel 11 via an inlet 13.
  • the solvent passes upwards through the biomass, contacting it and entraining biomass extract.
  • the solvent and extract mixture is conveyed via outlet 14 and delivery line 15 to the remainder of the extraction circuit of Figure 1.
  • the solvent/extract liquor passes via line 15 to the evaporator 12 of Figure 1.
  • a source of steam (e.g. a factory steam supply or a steam generator) is also connectable to inlet 13 from a line 19. This is achieved, e.g. by means of a flow control valve 17 to which both the solvent line 18 and steam line 19 are connected.
  • the flow control valve is operable e.g. under computer control to direct either the solvent from line 18 or the steam in line 19 via the inlet 13.
  • steam line 19 is connectable to supply steam, at atmospheric or super- atmospheric pressure, to the biomass in vessel 11
  • Steam line 19 includes an optional drain valve 27 for draining fluid from line 19.
  • a flow control valve 20 is operable e.g. under computer control to connect the outlet 14 to the solvent/extract delivery line 15; to suction or a vacuum (e.g. generated by a vacuum pump) 21 (for purposes described hereinbelow); or to a further steam line 23 for delivering steam, that has contacted the biomass, and solvent entrained therewith, to a separator in the form of a hollow container 24, in fluid communication with line 23 and containing an adsorbent material such as activated carbon.
  • valve 20 is controlled to connect outlet 14 to steam line 23, steam and solvent pass to container 24 where the adsorbent material separates the steam and solvent from one another.
  • the container 24 includes an outlet 25 remote from line 23, by means of which steam may pass to a condenser (not shown) and thence, in liquid form, to an effluent drain or reservoir.
  • the condenser may be operatively connected in line 23, upstream of contain 24, to permit condensation of the steam before removal of the solvent therefrom by means of the adsorbent material.
  • the apparatus may also optionally include a switchable recirculation loop for the steam, whereby the steam may be caused to contact the biomass more than once.
  • the re-circulation loop may be constituted by the line 26 shown dotted in Figure 2.
  • the flow of steam via line 26 may be deteirnined by e.g. computer controlled valves connecting line 26 to inlet 13 and outlet 14 at either end.
  • the extent of use of a given quantity of steam would be determined by the extent to which it becomes saturated with the solvent.
  • valve 17 is closed so that neither solvent (from line 18) nor steam (from line 19) enters vessel 11.
  • Outlet 14 is then connected, through operation of valve 20, to vacuum 20.
  • the bulk of liquid solvent in vessel 11 is consequently sucked out of vessel 11 by vacuum 20, until the solvent remaining in vessel 11 is constituted substantially by solvent adsorbed onto the biomass.
  • valve 20 operates to connect outlet 14 to line 23, and valve 17 operates to connect inlet 13 to steam line 19. Steam then flows into vessel 11 and contacts the biomass, thereby removing solvent from the biomass and conveying it via line 23 to the separator constituted by container 24 and the adsorbent material therein.
  • some or all of the steam may be recycled one or more times, using control of the various valves in the apparatus, so that the steam contacts the biomass more than once.
  • the condenser is in line 23 upstream of container 24, the steam is of course in liquid form by the time it contacts the adsorbent material. In this case there may be no need for subsequent condensing.
  • the biomass is discharged from the extraction vessel and the vessel recharged with fresh biomass and evacuated using vacuum 21 prior to introduction of fresh solvent from the extraction solvent circuit.
  • the adsorbent material may if desired be removed from the container 24 and heated to recover solvent therefrom.
  • the adsorbent material including adsorbed solvent may be disposed of in e.g. a landfill site or by incineration.
  • heat from the steam condenser may conveniently be used as a pre-heat for water in the steam generator.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Extraction Or Liquid Replacement (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
  • Processing Of Solid Wastes (AREA)
  • Detergent Compositions (AREA)

Abstract

In the field of biomass extraction, there is a need for effective removal of solvent from spent biomass material. An apparatus for removing solvent residues includes a vessel (11) for containing biomass; a steam source (19) for supplying steam to contact the biomass; and a separator (24) for separating solvent from steam that has contacted the biomass. The disclosure includes a method of use of the apparatus.

Description

APPARATUS AND METHOD FOR REMOVING SOLVENT RESIDUES
This invention concerns apparatuses and a method for removing solvent residues in particular after "extraction" of biomass. Biomass extraction is the extraction of flavours, fragrances or pharmaceutically active ingredients from materials of natural origin (these materials being referred to as "biomass".
Examples of biomass materials include but are not limited to flavoursome or aromatic substances such as coriander, cloves, star anise, coffee, orange juice, fennel seeds, cumin, ginger and other kinds of bark, leaves, flowers, fruit, roots, rhizomes and seeds. Biomass may also be extracted in the form of biologically active substances such as pesticides and pharmaceutically active substances or precursors thereto, obtainable e.g. from plant material, a cell culture or a fermentation broth.
There is growing technical and commercial interest in using near-critical solvents in such extraction processes. Examples of such solvents include liquefied carbon dioxide or, of particular interest, a family of solvents based on organic hydrofluorocarbon ("HFC") species.
By the term "hydrofluorocarbon" we are referring to materials which contain carbon, hydrogen and fluorine atoms only and which are thus chlorine-free.
Preferred hydrofluorocarbons are the hydrofluoroalkanes and particularly the Ci- 4 hydrofluoroalkanes. Suitable examples of Cι-4 hydrofluoroalkanes which may be used as solvents include, inter alia, trifluoromethane (R-23), fluoromethane (R-41), difluoromethane (R-32), pentafluoroefhane (R-125), 1 ,1,1- trifluoroethane (R-143a), 1,1,2,2-tetrafluoroethane (R-134), 1,1,1,2- tetrafluoroethane (R-134a), 1,1-difluoroethane (R-152a), heptafluoropropanes and particularly 1,1,1,2,3,3,3-heptafluoropropane (R-227ea), 1,1,1,2,3,3- hexafluoropropane (R-236ea), 1,1,1,2,2,3-hexafluoropropane (R-236cb), 1 ,1,1,3,3,3-hexafluoropropane (R-236fa), 1,1,1,3,3-pentafluoropropane (R- 245fa), 1 ,1,2,2,3-pentafluoropropane (R-245ca), 1,1,1,2,3-pentafluoropropane (R-245eb), 1,1,2,3,3-pentafluoropropane (R-245ea) and 1,1,1,3,3- pentafluorobutane (R-365mfc). Mixtures of two or more hydrofluorocarbons may be used if desired.
R-134a, R-227ea, R-32, R-125, R-245ca and R-245fa are preferred.
An especially preferred hydrofluorocarbon for use in the present invention is 1,1,1 ,2-tetrafluoroethane (R- 134a) .
It is possible to carry out biomass extraction using other solvents such as chlorofluorocarbons ("CFC's") and hydrochlorofluorocarbons ("HCFC's"), and/or mixtures of solvents. CFC's and HCFC's are not approved for food use and consequently are rarely employed in extraction processes in which the depleted biomass residue is intended as e.g. an animal feed.
Known extraction processes using solvents are normally carried out in closed- loop extraction equipment. A typical example 10 of such a system is shown schematically in Figure 1.
In this typical system, liquefied solvent is allowed to percolate by gravity in downflow through a bed of biomass held in vessel 11. Thence it flows to evaporator 12 where the volatile solvent is vaporised by heat exchange with a hot fluid. The vapour from evaporator 12 is then compressed by compressor 13. The compressed vapour is next fed to a condenser 14 where it is liquefied by heat exchange with a cold fluid. The liquefied solvent is then optionally collected in intermediate storage vessel 15 or returned (line 16) directly to the extraction vessel 1 to complete the circuit.
One of the key areas of concern relating to the use of solvents such as are used in biomass extraction processes is the level of residual solvent on the biomass material after extraction is complete. High levels of residual HFC (or other) solvent may be regarded as undesirable from a number of aspects:
• loss of HFC to atmosphere
• loss of HFC from the recycle process potentially increasing top-up costs
• landfill, incineration, composting and other biomass disposal regulatory issues • suitability of depleted biomass for use as an animal feedstuff supplement
In order to improve the rate of solvent extraction, the biomass is usually chopped or ground in some manner in order to increase the surface area in contact with the extraction solvent. Whilst beneficially increasing the rate of extraction of the desired components during biomass extraction, this increased surface area acts to increase the quantity of solvent that can remain adsorbed onto and in the biomass after extraction. Clearly some cost-effective method of achieving acceptable residual HFC solvent levels in the exhausted biomass would be of significant value in the development of the technology.
A combination of evacuation and heat (e.g. using a heating jacket surrounding extraction vessel 11) may act to reduce the levels of residual solvent in the biomass over a period of time. This method however has a number of potential disadvantages including:
• prolonged evacuation time to achieve low residue levels
• poor heat transfer into the packed-bed of biomass from the vessel jacket resulting in uneven heating and possible thermal deterioration of the biomass (charring, caramelisation etc.)
Such charring and caramelisation are particularly undesirable since they may adversely impact the commercial value of the biomass extracts.
According to the invention in a first aspect there is provided apparatus as defined in Claim 1.
In use of the apparatus steam advantageously strips solvent (that typically is an HFC such as 1,1,1,2- tetrafluoroethane, or mixtures of HFC's) from the biomass. The solvent is then entrained in the steam and conveyed to the separator, where the steam and the solvent are separated to allow recovery and/or disposal of the solvent.
In use of the apparatus the steam may contact the biomass once; or the apparatus may optionally include means such as pipework and valves permitting the steam to contact the biomass more than once.
Preferably the source of steam supplies steam at or near atmospheric pressure.
Alternatively the source of steam supplies steam at super-atmospheric pressure. In preferred embodiments the separator is or includes an adsorbent material for removing solvent entrained with the steam. More preferably the adsorbent material is or includes activated carbon. These features conveniently make the solvent available for recycling, or permit ready disposal of the solvent.
The adsorbent filter material may also act to reduce any volatilised organic materials present in the depleted biomass, again improving the quality of the effluent condensate. Depending on the nature of the adsorbent and on economic attractiveness, a concentrated stream of recovered HFC may be obtained from thermal regeneration of the adsorbent. Alternatively, the loaded adsorbent provides a convenient, compact and cost-effective package for appropriate disposal.
Claims 7 and 8 define optional forms of apparatus of the invention, that include a condenser either upstream or downstream of the separator, to condense the stream and facilitate separation of the steam and solvent from one another.
Claim 8 defines a preferred form of extractor vessel. The purpose of the optional connection to a vacuum or to suction is to permit evacuation of the vessel at the end of a biomass extraction, thereby removing from the vessel the bulk of the solvent therein. This means that the steam serves primarily to strip solvent that is adsorbed onto the surface of the biomass.
The vacuum connection may also advantageously be used to purge the vessel of e.g. water, when it is required to extract a new bed of biomass.
Preferably the extraction vessel is in use vertical, with the inlet at its lower end and the outlet at its upper end. This advantageously allows the charging of the extraction vessel with a packed bed of biomass. Such a packed bed may advantageously occupy substantially the entire cross-section of part of the vessel.
This arrangement has advantages in reducing the energy consumption of biomass extraction apparatus as shown in Figure 1.
The extraction vessel may optionally include a selectively operable condenser (cooling) jacket. This allows steam condensing advantageously to occur within the extraction vessel.
Preferably the extraction vessel includes thermal insulation. This advantageously reduces heat transfer from the vessel during both the biomass extraction and desorption (solvent recovery) processes.
According to a second aspect of the invention there is provided a method as defined in Claim 14. This method may conveniently be practised using apparatus as defined herein.
Further, advantageous features of the method are defined in Claims 15 to 22 and 24.
The method of the invention is superior to simple heating and/or evacuation, because
• the temperature of the biomass is raised rapidly and directly through intimate contact with steam
• steam flow acts to maintain a low partial pressure of HFC solvent in the vapour space around the biomass thus aiding transfer of HFC from the biomass to the steam stream • water from the steam is likely to act to displace HFC from the surface of the biomass through preferential adsorption thus further improving the rate and effectiveness of desorption relative to a flow of other gases such as nitrogen.
There now follows a description of a preferred embodiment of the invention, by way of non-limiting example, with reference being made to the accompanying drawings in which:
Figure 1 is a schematic representation of a prior art closed loop biomass extraction circuit; and
Figure 2 is a schematic representation of apparatus according to the invention, that may be included in the Figure 1 circuit.
Referring to Figure 2 there is shown a part of the Figure 1 circuit, modified in accordance with the invention. The remainder of the circuit part-illustrated in Figure 2 is as shown in Figure 1.
Figure 2 shows the extraction vessel 11 of the Figure 1 apparatus, in the form of a hollow cylinder, closed at each end 11a, lib and being in the preferred embodiment of flanged tube construction. In the preferred embodiment vessel 11 is vertical as shown, although other orientations, e.g. inclined or horizontal, are possible. A packed bed 12 of biomass is in use of the apparatus supported within extraction vessel 11, the cross-section of the packed bed 12 being substantially the same as that of the entire cross-section of the vessel 11 over a substantial part of its length. The vessel 11 is used for biomass extraction, during which solvent such as an HFC is fed into the bottom 11a of vessel 11 via an inlet 13. The solvent passes upwards through the biomass, contacting it and entraining biomass extract. The solvent and extract mixture is conveyed via outlet 14 and delivery line 15 to the remainder of the extraction circuit of Figure 1. In other words, the solvent/extract liquor passes via line 15 to the evaporator 12 of Figure 1.
A source of steam (e.g. a factory steam supply or a steam generator) is also connectable to inlet 13 from a line 19. This is achieved, e.g. by means of a flow control valve 17 to which both the solvent line 18 and steam line 19 are connected. The flow control valve is operable e.g. under computer control to direct either the solvent from line 18 or the steam in line 19 via the inlet 13.
Thus the steam line 19 is connectable to supply steam, at atmospheric or super- atmospheric pressure, to the biomass in vessel 11
Steam line 19 includes an optional drain valve 27 for draining fluid from line 19.
A flow control valve 20 is operable e.g. under computer control to connect the outlet 14 to the solvent/extract delivery line 15; to suction or a vacuum (e.g. generated by a vacuum pump) 21 (for purposes described hereinbelow); or to a further steam line 23 for delivering steam, that has contacted the biomass, and solvent entrained therewith, to a separator in the form of a hollow container 24, in fluid communication with line 23 and containing an adsorbent material such as activated carbon. When valve 20 is controlled to connect outlet 14 to steam line 23, steam and solvent pass to container 24 where the adsorbent material separates the steam and solvent from one another.
As shown in Figure 2 the container 24 includes an outlet 25 remote from line 23, by means of which steam may pass to a condenser (not shown) and thence, in liquid form, to an effluent drain or reservoir.
In an alternative embodiment the condenser may be operatively connected in line 23, upstream of contain 24, to permit condensation of the steam before removal of the solvent therefrom by means of the adsorbent material.
Other optional features of the apparatus, that may improve energy utilisation in use, include but are not limited to :
• heat recovery from the condensate into the steam generator feed water
• use of a jacket around the extraction vessel as the steam condenser to minimise condensation within the extraction vessel during desorption
• use of an insulated extraction vessel to maintain the internal temperature of the vessel during both extraction and desorption stages
The apparatus may also optionally include a switchable recirculation loop for the steam, whereby the steam may be caused to contact the biomass more than once. The re-circulation loop may be constituted by the line 26 shown dotted in Figure 2. The flow of steam via line 26 may be deteirnined by e.g. computer controlled valves connecting line 26 to inlet 13 and outlet 14 at either end. The extent of use of a given quantity of steam would be determined by the extent to which it becomes saturated with the solvent. In use of the apparatus of Figure 2, following completion of biomass extraction, valve 17 is closed so that neither solvent (from line 18) nor steam (from line 19) enters vessel 11.
Outlet 14 is then connected, through operation of valve 20, to vacuum 20. The bulk of liquid solvent in vessel 11 is consequently sucked out of vessel 11 by vacuum 20, until the solvent remaining in vessel 11 is constituted substantially by solvent adsorbed onto the biomass.
At this point valve 20 operates to connect outlet 14 to line 23, and valve 17 operates to connect inlet 13 to steam line 19. Steam then flows into vessel 11 and contacts the biomass, thereby removing solvent from the biomass and conveying it via line 23 to the separator constituted by container 24 and the adsorbent material therein.
If line 26 is present, some or all of the steam may be recycled one or more times, using control of the various valves in the apparatus, so that the steam contacts the biomass more than once.
After passing through the adsorbent material in container 24 the steam passes via line 25 for condensing and draining.
If the condenser is in line 23 upstream of container 24, the steam is of course in liquid form by the time it contacts the adsorbent material. In this case there may be no need for subsequent condensing.
After desorption of solvent from the biomass is complete, the biomass is discharged from the extraction vessel and the vessel recharged with fresh biomass and evacuated using vacuum 21 prior to introduction of fresh solvent from the extraction solvent circuit.
Following completion of the desorption process the adsorbent material may if desired be removed from the container 24 and heated to recover solvent therefrom.
Alternatively the adsorbent material including adsorbed solvent may be disposed of in e.g. a landfill site or by incineration.
If the apparatus includes a steam generator, heat from the steam condenser may conveniently be used as a pre-heat for water in the steam generator.

Claims

1. Apparatus for removing solvent residue from a bed of biomass, comprising an extraction vessel for containing biomass, that permits a solvent or a solvent mixture to contact biomass therein to effect extraction; a source of steam, selectively connectable to supply steam to biomass in the extraction vessel; a separator for separating steam, that has contacted biomass in the extraction vessel, and solvent entrained therewith; and a delivery line for steam/solvent selectively interconnectable between the extraction vessel and the separator to permit passage of steam and solvent entrained therewith to the separator.
2. Apparatus according to Claim 1 wherein the source of steam supplies steam at atmospheric pressure.
3. Apparatus according to Claim 1 wherein the source of steam supplies steam at super-atmospheric pressure.
4. Apparatus according to any preceding claim wherein the separator is or includes an adsorbent material for removmg solvent entrained with the steam.
5. Apparatus according to Claim 4 wherein the adsorbent material is or includes activated carbon.
6. Apparatus according to Claim 4 or Claim 5 wherein the separator includes an inlet for receiving steam and solvent from the extraction vessel and an outlet, the outlet being operatively connected to a condenser to condense the steam after removal of the solvent therefrom by means of the separator.
7. Apparatus according to any of Claims 1 to 5 including a condenser operatively connected in series with and upstream of the separator, whereby the steam is condensed before removal of solvent therefrom by means of the separator.
8. Apparatus according to any preceding claim wherein the extraction vessel is a cylindrical chamber closed at either end and having an inlet at one end and an outlet at its other end, the hollow interior of the chamber being for containing biomass, the inlet being selectively connectable to a source of solvent and a source of steam; and the outlet being selectively connectable as part of a circuit for recovering biomass extract; to a vacuum; or to the said separator.
9. Apparatus according to Claim 8, wherein the extraction vessel is in use vertical, with the inlet at its lower end and the outlet at its upper end.
10. Apparatus according to any preceding claim, wherein the extraction vessel contains a packed bed of biomass.
11. Apparatus according to Claim 10 wherein the packed bed of biomass occupies substantially the entire cross-section of at least a portion of the extraction vessel.
12. Apparatus according to any preceding claim including a steam condenser jacket around at least part of the extraction vessel.
13. Apparatus according to any preceding claim including thermal insulation for the extraction vessel.
14. A method of removing solvent residues from a bed of biomass, comprising contacting the biomass with steam; passing the steam, in vapour or liquid form, and solvent entrained therewith, to a separator; and separating the steam and the solvent from one another in the separator.
15. A method according to Claim 14 wherein the step of separating includes contacting an adsorbent with the steam/solvent mixture.
16. A method according to Claim 14 or Claim 15 including the step of condensing the steam after passing it to the separator.
17. A method according to Claim 14 or Claim 15 including the step of condensing the steam before passing it to the separator.
18. A method according to Claim 17 wherein the condensing occurs within a vessel containing the biomass.
19. A method according to Claim 14 or any claim dependent therefrom, wherein the step of contacting the biomass with steam occurs in a vessel, and the method includes the step of partially or substantially evacuating the vessel before the steam contacts the biomass.
20. A method according to Claim 15 or any claim dependent therefrom, including the step of heating the adsorbent to recover solvent therefrom.
21. A method according to any of Claims 15 to 19 including the step of disposing of the adsorbent and the solvent therewith.
22. A method according to Claim 16 or Claim 17 or any claim dependent therefrom, wherein the step of condensing the steam includes recovering heat from the condensate and using the recovered heat to pre-heat water for steam generation.
23. Solvent recovered by the method of any of Claims 14 to 20, Claim 22 when dependent from any of Claims 14 to 20.
PCT/GB2000/003319 1999-09-06 2000-08-31 Apparatus and method for removing solvent residues WO2001017643A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
MXPA02002431A MXPA02002431A (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residues.
CA002383588A CA2383588A1 (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residues
AT00956674T ATE273736T1 (en) 1999-09-06 2000-08-31 DEVICE AND METHOD FOR REMOVAL OF SOLVENT REMAIN
AU68545/00A AU766475C (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residues
BR0013803-7A BR0013803A (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residue from a biomass bed, and, solvent
JP2001521425A JP2003508205A (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residue
IL14843700A IL148437A0 (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residues
DE60013146T DE60013146T2 (en) 1999-09-06 2000-08-31 DEVICE AND METHOD FOR REMOVING SOLVENT RESIDUES
EP00956674A EP1212127B1 (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residues
KR1020027002980A KR20020042825A (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residues

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9920949.6A GB9920949D0 (en) 1999-09-06 1999-09-06 Apparatus and method for removing solvent residues
GB9920949.6 1999-09-06

Publications (1)

Publication Number Publication Date
WO2001017643A1 true WO2001017643A1 (en) 2001-03-15

Family

ID=10860376

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB2000/003319 WO2001017643A1 (en) 1999-09-06 2000-08-31 Apparatus and method for removing solvent residues

Country Status (17)

Country Link
US (2) US6685839B1 (en)
EP (1) EP1212127B1 (en)
JP (1) JP2003508205A (en)
KR (1) KR20020042825A (en)
CN (1) CN1420799A (en)
AT (1) ATE273736T1 (en)
AU (1) AU766475C (en)
BR (1) BR0013803A (en)
CA (1) CA2383588A1 (en)
DE (1) DE60013146T2 (en)
ES (1) ES2226906T3 (en)
GB (2) GB9920949D0 (en)
IL (1) IL148437A0 (en)
MX (1) MXPA02002431A (en)
RU (1) RU2223134C2 (en)
WO (1) WO2001017643A1 (en)
ZA (1) ZA200201745B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7001511B2 (en) 1999-09-06 2006-02-21 Ineous Fluor Holdings Limited Apparatus and method for removing solvent residues

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT1473071E (en) * 2003-04-30 2008-03-11 Air Prod & Chem Method and system for purifying exhaust gas
ITMO20040202A1 (en) * 2004-07-30 2004-10-30 Illycaffe Spa METHODS AND APPARATUS FOR OBTAINING DRINKS.
CA2767125A1 (en) * 2009-07-02 2011-01-06 Bioexx Specialty Proteins Ltd. Process for removing organic solvents from a biomass
GB201002617D0 (en) * 2010-02-16 2010-03-31 Ineos Fluor Holdings Ltd Heat transfer compositions
GB201002616D0 (en) * 2010-02-16 2010-03-31 Ineos Fluor Holdings Ltd Heat transfer compositions
CN103830931A (en) * 2012-11-27 2014-06-04 张勇 Full-automatic extraction-evaporation device
RU2665739C1 (en) * 2017-07-03 2018-09-04 Олег Владимирович Борисенко Borisenko's non-buried water engine
US11865474B2 (en) * 2021-03-24 2024-01-09 Gene Pool Technologies , Inc. Residual solvent recovery apparatuses and methods

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH289059A (en) * 1948-10-01 1953-02-28 Metallgesellschaft Ag System for the recovery of the solvent in the extraction of solid products.
US4289505A (en) * 1980-06-13 1981-09-15 Air Resources, Inc. Solvent recovery from water
DE3538745A1 (en) * 1985-10-31 1987-05-07 Extraktionstechnik Gmbh METHOD AND SYSTEM FOR WATER-FREE SOLID EXTRACTION WITH ORGANIC SOLVENTS

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB211417A (en) 1923-09-10 1924-02-21 William Davis Moore Method and apparatus for facing foundry moulds
US1977411A (en) * 1934-01-08 1934-10-16 Howard G Smith Boiler
US3612066A (en) 1970-02-05 1971-10-12 Reynolds Tobacco Co R Denicotinizing process
US3669679A (en) 1970-04-24 1972-06-13 Gen Foods Corp Green bean decaffeination employing fluorinated hydrocarbons
US3671263A (en) * 1971-02-23 1972-06-20 Procter & Gamble Semi-continuous countercurrent decaffeination process
AT331374B (en) * 1972-12-22 1976-08-25 Studiengesellschaft Kohle Mbh PROCESS FOR THE PRODUCTION OF FATS AND OILS FROM VEGETABLE AND ANIMAL PRODUCTS
CA1079008A (en) * 1975-10-24 1980-06-10 Cp Associates Limited Solvent pulping process
CA1140919A (en) * 1980-05-15 1983-02-08 Du Pont Canada Inc. Control of residual solvent in proteinaceous materials
DE3045877A1 (en) * 1980-12-05 1982-07-08 Linde Ag, 6200 Wiesbaden Solvent residue removed from bulk material - by steam with partial recycling through compressor and reheater, used esp. for removing per:chloroethylene from bones
US4539816A (en) * 1981-04-03 1985-09-10 Minnesota Mining And Manufacturing Company Heat and liquid recovery using open cycle heat pump system
US4486453A (en) * 1982-12-27 1984-12-04 The Procter & Gamble Company Desolventizing process
US4802975A (en) * 1984-03-29 1989-02-07 Amoco Corporation Method for stripping of residual solvent
US5092983A (en) 1986-09-12 1992-03-03 The Standard Oil Company Process for separating extractable organic material from compositions comprising said extractable organic material intermixed with solids and water using a solvent mixture
US5281732A (en) 1991-12-31 1994-01-25 University Research & Marketing Solvent extraction of oil from oil-bearing materials
US5516923A (en) 1992-04-27 1996-05-14 Agritech International Extracting oil from oil bearing plant parts
US5440055A (en) 1993-03-12 1995-08-08 Aphios Corporation Method and apparatus for extracting taxol from source materials
GB9618576D0 (en) * 1996-09-05 1996-10-16 Boc Group Plc Air separation
GB9920949D0 (en) 1999-09-06 1999-11-10 Ici Ltd Apparatus and method for removing solvent residues

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH289059A (en) * 1948-10-01 1953-02-28 Metallgesellschaft Ag System for the recovery of the solvent in the extraction of solid products.
US4289505A (en) * 1980-06-13 1981-09-15 Air Resources, Inc. Solvent recovery from water
DE3538745A1 (en) * 1985-10-31 1987-05-07 Extraktionstechnik Gmbh METHOD AND SYSTEM FOR WATER-FREE SOLID EXTRACTION WITH ORGANIC SOLVENTS

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7001511B2 (en) 1999-09-06 2006-02-21 Ineous Fluor Holdings Limited Apparatus and method for removing solvent residues

Also Published As

Publication number Publication date
ES2226906T3 (en) 2005-04-01
MXPA02002431A (en) 2002-07-30
EP1212127A1 (en) 2002-06-12
ATE273736T1 (en) 2004-09-15
IL148437A0 (en) 2002-09-12
ZA200201745B (en) 2003-05-28
RU2223134C2 (en) 2004-02-10
US20040016704A1 (en) 2004-01-29
EP1212127B1 (en) 2004-08-18
AU766475C (en) 2004-09-09
AU766475B2 (en) 2003-10-16
AU6854500A (en) 2001-04-10
JP2003508205A (en) 2003-03-04
BR0013803A (en) 2002-05-21
GB0021141D0 (en) 2000-10-11
DE60013146D1 (en) 2004-09-23
CA2383588A1 (en) 2001-03-15
US7001511B2 (en) 2006-02-21
GB9920949D0 (en) 1999-11-10
GB2353731A (en) 2001-03-07
US6685839B1 (en) 2004-02-03
GB2353731B (en) 2001-10-31
CN1420799A (en) 2003-05-28
KR20020042825A (en) 2002-06-07
DE60013146T2 (en) 2005-09-01

Similar Documents

Publication Publication Date Title
US6589422B2 (en) Apparatus and method for extracting biomass
US6676838B2 (en) Apparatus and methods for removing solvent residues
US20060124544A1 (en) System for liquid extraction, and methods
AU766475C (en) Apparatus and method for removing solvent residues
EP1345665B1 (en) Apparatus and method for extracting biomass
US6521022B1 (en) Apparatus and method for reducing residual solvent levels
GB2353735A (en) Apparatus and method for extracting biomass

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CR CU CZ DE DK DM DZ EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2000956674

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 148437

Country of ref document: IL

Ref document number: 2383588

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 2002/01745

Country of ref document: ZA

Ref document number: 200201745

Country of ref document: ZA

WWE Wipo information: entry into national phase

Ref document number: IN/PCT/2002/00271/DE

Country of ref document: IN

ENP Entry into the national phase

Ref document number: 2001 521425

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 68545/00

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: PA/a/2002/002431

Country of ref document: MX

Ref document number: 1020027002980

Country of ref document: KR

ENP Entry into the national phase

Ref document number: 2002 2002108732

Country of ref document: RU

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 008150745

Country of ref document: CN

WWP Wipo information: published in national office

Ref document number: 1020027002980

Country of ref document: KR

WWP Wipo information: published in national office

Ref document number: 2000956674

Country of ref document: EP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWG Wipo information: grant in national office

Ref document number: 68545/00

Country of ref document: AU

WWG Wipo information: grant in national office

Ref document number: 2000956674

Country of ref document: EP