WO2005092466A1 - A process for the extraction of ethanol from a water solution - Google Patents

A process for the extraction of ethanol from a water solution Download PDF

Info

Publication number
WO2005092466A1
WO2005092466A1 PCT/SE2005/000425 SE2005000425W WO2005092466A1 WO 2005092466 A1 WO2005092466 A1 WO 2005092466A1 SE 2005000425 W SE2005000425 W SE 2005000425W WO 2005092466 A1 WO2005092466 A1 WO 2005092466A1
Authority
WO
WIPO (PCT)
Prior art keywords
ethanol
solution
salt
bed
alcohol
Prior art date
Application number
PCT/SE2005/000425
Other languages
French (fr)
Inventor
Michail Gougel
Giuliano Grassi
Original Assignee
Globelive International Ab
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 Globelive International Ab filed Critical Globelive International Ab
Priority to DE602005011947T priority Critical patent/DE602005011947D1/en
Priority to EP05722261A priority patent/EP1737549B1/en
Priority to US10/599,308 priority patent/US7462749B2/en
Publication of WO2005092466A1 publication Critical patent/WO2005092466A1/en

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/04—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
    • B01J20/048—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium containing phosphorus, e.g. phosphates, apatites, hydroxyapatites
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/30—Processes for preparing, regenerating, or reactivating
    • B01J20/34—Regenerating or reactivating
    • B01J20/3433—Regenerating or reactivating of sorbents or filter aids other than those covered by B01J20/3408 - B01J20/3425
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/30—Processes for preparing, regenerating, or reactivating
    • B01J20/34—Regenerating or reactivating
    • B01J20/3483—Regenerating or reactivating by thermal treatment not covered by groups B01J20/3441 - B01J20/3475, e.g. by heating or cooling
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00—Fermentation processes for beer
    • C12C11/02—Pitching yeast
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00—Technologies for the production of fuel of non-fossil origin
    • Y02E50/10—Biofuels, e.g. bio-diesel

Definitions

  • the invention refers to a process for extraction of an ethanol from a solution thereof, according to the preamble of appended Claim 1.
  • the separation of ethanol from a low-grade ethyl-alcohol solution is attractive for several reasons.
  • the ethanol for example bio-ethanol
  • a mash is produced, comprising i.a. a solution, having a relatively low concentration of ethyl-alcohol (in general 5%-12%) .
  • bio-ethanol is obtained by a fermentation of a C-6 sugar/water solution having a low concentration (10-25%) .
  • the liquid mixture or solution from which the ethanol is extracted sometimes represents a co-product, the usefulness and market value of which is improved by said extraction of alcohol.
  • Another problem is that one or more properties of the liquid, from which the ethanol is extracted, are affected in a negative sense, by usual present extraction processes, in which the liquid is heated and alcohol is extracted by distillation up to, e.g. 96% (azeotropic bio-ethanol) . Further processing to produce net bio-ethanol 100% can be performed by the use of molecular sieves.
  • One object of the invention is therefore to provide a process by which the energy consumption for the extraction of an ethanol from a solution is improved.
  • a further object is to produce high-grade ethanol, in particular bio-ethanol from a low-grade solution by a one-step process.
  • a further object is to provide a process in which the solution from which the ethanol is extracted does not have to be heated. The objects are, at least to some degree, reached by the invention.
  • An important feature of the invention is that the initial low-grade solution (mash) is brought into contact with a particle bed of a specific salt, namely Mg 3 (P0 4 ) 2 .
  • Mg 3 (P0 4 ) 2 chemically binds ethanol molecules from a solution. Since the salt chemically binds practically only ethanol, even from a low- grade alcohol solution, the ethanol vapour subsequently driven off from the bed will be high-grade. The ethanol vapour driven off from the salt bed is then collected and preferably condensed into liquid form.
  • the energy required to produce the ethanol is relatively small, since only the salt bed with the adsorbed ethanol has to be heated (not all of the solution) to release the ethanol, chemically bound ("adsorbed") in the salt.
  • the valuable product of the process can be the high-grade ethanol and/or solution from which the ethanol has been adsorbed.
  • the removal of ethanol from the solution can sometimes be considered as a product improvement, especially since the solution is not heated by the process, so that the remaining content of the solution is not damaged by heating.
  • the solution could consist of a mash, which after adsorption of ethanol can be processed to obtain a useful animal feed product .
  • the salt bed can be kept under partial vacuum in order to reduce further the heating necessary to evaporate the ethanol .
  • Fig. 1 illustrates schematically the construction of a device for performing the inventive process.
  • the device according to fig. 1 is comprised of a closed vessel 1, provided with a perforated partition wall 2 that divides the vessel vertically into two parts, a bottom part 3 and a top part 4. Disposed in the top part 4 of the vessel, above the perforated partition wall 2 are heatable elements 6 and a layer or bed of salt 5, that will preferentially adsorb ethanol from a low-grade solution.
  • the salt bed is in direct contact with the heatable elements 6.
  • the elements 6 are heated by some energy source 7.
  • the energy source 7 could be a burner from which a flue gas is passed through elements 6 in the form of pipes which extend to a controllable valve device 11 for controling the gas flow through the pipes 6, in order to control the heat supply through the pipes 6.
  • Heat from the source 7 is delivered into the bed 5 through the pipe wall.
  • a liquid portion of the mash is delivered to the vessel 1 through a closable pipe 8, and a closable pipe 9 is provided for carrying away ethanol vapour, said pipes being placed in the upper part 4 of the vessel, above the salt bed 5.
  • the salt bed 5 comprises a layer of salt granules.
  • a pipe 10 is provided for carrying away the mash from which ethanol has been adsorbed by the salt and that has been collected in the lower part 3 of the vessel.
  • the device operates in the following way.
  • the mash liquid is delivered to the pipe 8 connected to the upper part 4 of the vessel.
  • the mash fluid passes through the bed of salt.
  • the salt preferentially adsorbs ethanol from the mash liquid.
  • the remainder of the mash delivered to the vessel, said mash now having a lower alcohol concentration is drained off from the salt bed and is carried away from the bottom part 3 of the vessel through the pipe 10.
  • the mash liquid can be contacted with the salt bed to such an amount that essentially all of the ethanol content thereof is adsorbed by the salt bed, whereby the mash liquid drained off from the salt bed has an essentially ethyl-alcohol content of 0%.
  • the ethanol content of a flow of mash liquid that leaves the apparatus after having passed through the salt bed can be sensed. As soon as the ethanol content sensed raises significantly above 0%, the ethanol adsorption capacity of the bed can be considered exhausted. Then the input of mash liquid is stopped.
  • the heat is delivered from a heat source 7 to the heatable element 6, whereby the salt of the salt bed 5 emits the adsorbed ethanol. If the heat source is a burner or the like, the flue gas flow can be controlled by the valve device 11.
  • the ethanol alcohol is evacuated through the pipe 9. This ethanol vapour is converted, by cooling, into a condensate.
  • the high-grade alcohol thus formed can be used as a fuel, for example.
  • On advantage of the invention is that only the salt bed with adsorbed ethanol has to be heated (not all of the mash liquid) , and a further advantage is that the heating process performed to drive off the ethanol adsorbed by the salt also regenerates the salt for a new cycle.
  • Trials have shown that the salt should have a solubility product of not higher than 10 "24 , since otherwise the salt dissolution and the need to add new salt crystals to the bed will be disturbing.
  • Mg 3 (P0 ) 2 is the preferred salt used in the present invention, has such a solubility product.
  • the heatable elements can be heated by energy from conventional sources or preferably from renewable energy in particular bioenergy for example, by fuel pellets which preferably are made from renewable biological material, for example agro-forestry residues.
  • the device shown on the drawing constitutes a system for batch operation. However, it is obvious that two such devices could be connected in parallel and driven in sequence in opposite phases in order to provide a continuous production of alcohol.

Abstract

A process for the extraction of ethanol from a solution by bringing the solution into contact with a bed of salt (5) consisting of Mg3(PO4)2, whereby the salt adsorbs ethanol from the solution, removing the solution from the salt bed, heating of the salt bed in order to release the ethanol adsorbed thereby as vapour and collecting the ethanol vapour.

Description

A PROCESS FOR THE EXTRACTION OF ETHANOL FROM A WATER SOLUTION
The invention refers to a process for extraction of an ethanol from a solution thereof, according to the preamble of appended Claim 1.
The separation of ethanol from a low-grade ethyl-alcohol solution is attractive for several reasons. First, the ethanol, for example bio-ethanol, can to advantage be produced by biochemical processes, such as fermentation of a mixture of water and sugars (or from starches or ligno- cellulosic feedstock) . By fermentation of the mixture, a mash is produced, comprising i.a. a solution, having a relatively low concentration of ethyl-alcohol (in general 5%-12%) . Usually, bio-ethanol is obtained by a fermentation of a C-6 sugar/water solution having a low concentration (10-25%) . By extracting high-grade alcohol from the low-grade solution, a useful product is obtained, which can be used i.a. as fuel. Moreover, the liquid mixture or solution from which the ethanol is extracted sometimes represents a co-product, the usefulness and market value of which is improved by said extraction of alcohol.
One problem is however the costs for the extraction of high- grade ethanol from such low-grade solutions .
Another problem is that one or more properties of the liquid, from which the ethanol is extracted, are affected in a negative sense, by usual present extraction processes, in which the liquid is heated and alcohol is extracted by distillation up to, e.g. 96% (azeotropic bio-ethanol) . Further processing to produce net bio-ethanol 100% can be performed by the use of molecular sieves. One object of the invention is therefore to provide a process by which the energy consumption for the extraction of an ethanol from a solution is improved. A further object is to produce high-grade ethanol, in particular bio-ethanol from a low-grade solution by a one-step process. A further object is to provide a process in which the solution from which the ethanol is extracted does not have to be heated. The objects are, at least to some degree, reached by the invention.
The invention is defined in the appended independent claims.
Embodiments of the invention are defined in the appended depending claims.
An important feature of the invention is that the initial low-grade solution (mash) is brought into contact with a particle bed of a specific salt, namely Mg3(P04)2.
It has now surprisingly been found that Mg3(P04)2 chemically binds ethanol molecules from a solution. Since the salt chemically binds practically only ethanol, even from a low- grade alcohol solution, the ethanol vapour subsequently driven off from the bed will be high-grade. The ethanol vapour driven off from the salt bed is then collected and preferably condensed into liquid form.
The energy required to produce the ethanol is relatively small, since only the salt bed with the adsorbed ethanol has to be heated (not all of the solution) to release the ethanol, chemically bound ("adsorbed") in the salt.
The valuable product of the process can be the high-grade ethanol and/or solution from which the ethanol has been adsorbed. The removal of ethanol from the solution can sometimes be considered as a product improvement, especially since the solution is not heated by the process, so that the remaining content of the solution is not damaged by heating.
The solution could consist of a mash, which after adsorption of ethanol can be processed to obtain a useful animal feed product .
The salt bed can be kept under partial vacuum in order to reduce further the heating necessary to evaporate the ethanol .
One embodiment of the invention will now be described with reference to an extraction device.
Fig. 1 illustrates schematically the construction of a device for performing the inventive process.
The device according to fig. 1 is comprised of a closed vessel 1, provided with a perforated partition wall 2 that divides the vessel vertically into two parts, a bottom part 3 and a top part 4. Disposed in the top part 4 of the vessel, above the perforated partition wall 2 are heatable elements 6 and a layer or bed of salt 5, that will preferentially adsorb ethanol from a low-grade solution. The salt bed is in direct contact with the heatable elements 6. The elements 6 are heated by some energy source 7. For example, the energy source 7 could be a burner from which a flue gas is passed through elements 6 in the form of pipes which extend to a controllable valve device 11 for controling the gas flow through the pipes 6, in order to control the heat supply through the pipes 6. Heat from the source 7 is delivered into the bed 5 through the pipe wall. A liquid portion of the mash is delivered to the vessel 1 through a closable pipe 8, and a closable pipe 9 is provided for carrying away ethanol vapour, said pipes being placed in the upper part 4 of the vessel, above the salt bed 5. The salt bed 5 comprises a layer of salt granules. A pipe 10 is provided for carrying away the mash from which ethanol has been adsorbed by the salt and that has been collected in the lower part 3 of the vessel.
The device operates in the following way. The mash liquid is delivered to the pipe 8 connected to the upper part 4 of the vessel. The mash fluid passes through the bed of salt. The salt preferentially adsorbs ethanol from the mash liquid. The remainder of the mash delivered to the vessel, said mash now having a lower alcohol concentration is drained off from the salt bed and is carried away from the bottom part 3 of the vessel through the pipe 10. The mash liquid can be contacted with the salt bed to such an amount that essentially all of the ethanol content thereof is adsorbed by the salt bed, whereby the mash liquid drained off from the salt bed has an essentially ethyl-alcohol content of 0%. The ethanol content of a flow of mash liquid that leaves the apparatus after having passed through the salt bed, can be sensed. As soon as the ethanol content sensed raises significantly above 0%, the ethanol adsorption capacity of the bed can be considered exhausted. Then the input of mash liquid is stopped. The heat is delivered from a heat source 7 to the heatable element 6, whereby the salt of the salt bed 5 emits the adsorbed ethanol. If the heat source is a burner or the like, the flue gas flow can be controlled by the valve device 11. The ethanol alcohol is evacuated through the pipe 9. This ethanol vapour is converted, by cooling, into a condensate. The high-grade alcohol thus formed can be used as a fuel, for example. On advantage of the invention is that only the salt bed with adsorbed ethanol has to be heated (not all of the mash liquid) , and a further advantage is that the heating process performed to drive off the ethanol adsorbed by the salt also regenerates the salt for a new cycle. Trials have shown that the salt should have a solubility product of not higher than 10"24, since otherwise the salt dissolution and the need to add new salt crystals to the bed will be disturbing. Mg3(P0 )2 is the preferred salt used in the present invention, has such a solubility product.
The heatable elements can be heated by energy from conventional sources or preferably from renewable energy in particular bioenergy for example, by fuel pellets which preferably are made from renewable biological material, for example agro-forestry residues.
In the drawing, the mash liquid flow is indicated with full arrows, while the vapour flow is indicated with broken arrows in the drawing.
The device shown on the drawing constitutes a system for batch operation. However, it is obvious that two such devices could be connected in parallel and driven in sequence in opposite phases in order to provide a continuous production of alcohol.

Claims

1. A process for the extraction of ethanol from a solution, characterized by bringing the solution into contact with a bed of salt, whereby the salt adsorbs ethanol from the solution, removing the solution from the salt bed, heating of the salt bed in order to release the ethanol adsorbed thereby as vapour and collecting the ethanol.
2. A process according to Claim 1, characterized in that the salt is Mg3(P0 )2-
3. A process according to Claim 1 or 2 , characterized in that the salt preferentially adsorbs ethanol molecules from a low-grade ethyl-alcohol solution, whereby high-grade ethanol can be obtained from the low concentration alcohol solution, in a one-step process.
4. A process according to any of Claims 1-3, characterized in that the solution consists of a low-grade ethyl-alcohol liquid which has been separated from a mash.
5. A process according to any of Claims 1-4, characterized by passing a flow of the solution through the bed, sensing the ethyl-alcohol content of the solution leaving the bed, and stopping the input flow to the bed when the sensed alcohol content of the solution leaving the bed significantly raises above 0%, and collecting the solution leaving the bed and having an alcohol content of about 0%,
PCT/SE2005/000425 2004-03-25 2005-03-23 A process for the extraction of ethanol from a water solution WO2005092466A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
DE602005011947T DE602005011947D1 (en) 2004-03-25 2005-03-23 PROCESS FOR EXTRACTION OF ETHANOL FROM AN AQUEOUS SOLUTION
EP05722261A EP1737549B1 (en) 2004-03-25 2005-03-23 A process for the extraction of ethanol from a water solution
US10/599,308 US7462749B2 (en) 2004-03-25 2005-03-23 Process for the extraction of ethanol from a water solution

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0400775-3 2004-03-25
SE0400775A SE527535C2 (en) 2004-03-25 2004-03-25 Procedure for extracting alcohol from a solution

Publications (1)

Publication Number Publication Date
WO2005092466A1 true WO2005092466A1 (en) 2005-10-06

Family

ID=32067527

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SE2005/000425 WO2005092466A1 (en) 2004-03-25 2005-03-23 A process for the extraction of ethanol from a water solution

Country Status (7)

Country Link
US (1) US7462749B2 (en)
EP (1) EP1737549B1 (en)
AT (1) ATE418371T1 (en)
DE (1) DE602005011947D1 (en)
ES (1) ES2318471T3 (en)
SE (1) SE527535C2 (en)
WO (1) WO2005092466A1 (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4492637A (en) * 1983-11-25 1985-01-08 The Board Of Regents Of The University Of Nebraska Water separation process
US4874524A (en) * 1988-03-30 1989-10-17 The Curators Of The University Of Missouri Separation of adsorbed components by variable temperature desorption
DD274362A1 (en) * 1988-07-27 1989-12-20 Univ Halle Wittenberg RELEASE AGENT FOR ETHYL ALCOHOL WATER MIXTURES
US5421860A (en) * 1992-05-22 1995-06-06 Engelhard Process Chemicals Gmbh Sorption of organic compounds from fluids
US5427689A (en) * 1994-10-17 1995-06-27 Phillips Petroleum Company Separation of polar substances from hydrocarbons
WO2001034267A1 (en) * 1999-11-11 2001-05-17 Gougel Industri Ab A system and a device for desalination of water

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4492637A (en) * 1983-11-25 1985-01-08 The Board Of Regents Of The University Of Nebraska Water separation process
US4874524A (en) * 1988-03-30 1989-10-17 The Curators Of The University Of Missouri Separation of adsorbed components by variable temperature desorption
DD274362A1 (en) * 1988-07-27 1989-12-20 Univ Halle Wittenberg RELEASE AGENT FOR ETHYL ALCOHOL WATER MIXTURES
US5421860A (en) * 1992-05-22 1995-06-06 Engelhard Process Chemicals Gmbh Sorption of organic compounds from fluids
US5427689A (en) * 1994-10-17 1995-06-27 Phillips Petroleum Company Separation of polar substances from hydrocarbons
WO2001034267A1 (en) * 1999-11-11 2001-05-17 Gougel Industri Ab A system and a device for desalination of water

Also Published As

Publication number Publication date
US7462749B2 (en) 2008-12-09
US20070205093A1 (en) 2007-09-06
SE527535C2 (en) 2006-04-04
SE0400775D0 (en) 2004-03-25
ATE418371T1 (en) 2009-01-15
EP1737549B1 (en) 2008-12-24
ES2318471T3 (en) 2009-05-01
EP1737549A1 (en) 2007-01-03
SE0400775L (en) 2005-09-26
DE602005011947D1 (en) 2009-02-05

Similar Documents

Publication Publication Date Title
US7572353B1 (en) Ethanol distillation process
US4277635A (en) Process of concentrating ethanol from dilute aqueous solutions thereof
US7867365B2 (en) Ethanol distillation with distillers soluble solids recovery apparatus
US4345973A (en) Vapor phase dehydration of aqueous alcohol mixtures
Jeong et al. Production of anhydrous ethanol using various PSA (Pressure Swing Adsorption) processes in pilot plant
WO1986003686A1 (en) Bulk removal of water from organic liquids
JP6628604B2 (en) Purification of succinic acid
WO2010096626A1 (en) Use of pressure swing absorption for water removal from a wet methanol stream
WO2013177056A1 (en) Process and adsorbent for separating ethanol and associated oxygenates from a biofermentation system
JP2021116246A (en) Purified 1,3-butanediol and its manufacturing method
EP1737549B1 (en) A process for the extraction of ethanol from a water solution
CN108976144A (en) A kind of method of biopharmaceutical production DMF waste liquid purification
GB2096125A (en) Multi-stage adsorption process for separating organic liquids from water
EP0081211B1 (en) Concentration of organic chemicals from dilute aqueous solutions
US5030775A (en) Process for preparing motor fuel grade alcohol
CN106458829A (en) Method for extracting ferulic acid and/or salts of same
Abdeen et al. Dehydration of ethanol on zeolite based media using adsorption process
CN102417450A (en) Method for purifying chromatographic grade butyl acetate
CN207891287U (en) A kind of catalyst mother liquor comprehensive recycling device in propenecarbonyl
CN1106712A (en) Process for separating components of a liquid mixture
Ladadok et al. Kinetics, isotherm and thermodynamics of sterol adsorption on styrene-divinylbenzene anion-exchange resins.
CN101255096A (en) Method for purifying and reclaiming alcohol from weak liquor by activated charcoal adsorption-microwave azeotropic distillation desorption
RU2037000C1 (en) Fibrous semi-finished product production method
Tadayon et al. DESIGN OF ADSORPTIVE DISTILLATION FOR SEPARATION OF ETHANOL-WATER AZEOTROPIC MIXTURE USING BIO-BASED ADSORBENTS.
SK288853B6 (en) Apparatus for concentrating volatile organic compounds by adsorption and desorption and a method for concentrating volatile organic compounds by adsorption and desorption

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 BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG 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 NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

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

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2005722261

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 10599308

Country of ref document: US

Ref document number: 2007205093

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Ref document number: DE

WWP Wipo information: published in national office

Ref document number: 2005722261

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 10599308

Country of ref document: US