NO326769B1 - Blanding egnet for ekstrahering av eddiksyre fra en vandig strom, fremgangsmate for a oppna eddiksyre fra en vandig fase samt fermenteringsprosess for fremstilling av eddiksyre - Google Patents
Blanding egnet for ekstrahering av eddiksyre fra en vandig strom, fremgangsmate for a oppna eddiksyre fra en vandig fase samt fermenteringsprosess for fremstilling av eddiksyre Download PDFInfo
- Publication number
- NO326769B1 NO326769B1 NO20011161A NO20011161A NO326769B1 NO 326769 B1 NO326769 B1 NO 326769B1 NO 20011161 A NO20011161 A NO 20011161A NO 20011161 A NO20011161 A NO 20011161A NO 326769 B1 NO326769 B1 NO 326769B1
- Authority
- NO
- Norway
- Prior art keywords
- solvent
- acetic acid
- water
- mixture
- hydrogen
- Prior art date
Links
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 title claims abstract description 624
- 239000000203 mixture Substances 0.000 title claims abstract description 119
- 238000000034 method Methods 0.000 title claims abstract description 113
- 238000000855 fermentation Methods 0.000 title claims abstract description 109
- 230000004151 fermentation Effects 0.000 title claims abstract description 107
- 238000000605 extraction Methods 0.000 title claims abstract description 86
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 39
- 239000008346 aqueous phase Substances 0.000 title claims description 51
- 230000008569 process Effects 0.000 title claims description 49
- 239000002904 solvent Substances 0.000 claims abstract description 368
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims abstract description 162
- 239000006184 cosolvent Substances 0.000 claims abstract description 148
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 82
- 229910002092 carbon dioxide Inorganic materials 0.000 claims abstract description 81
- 239000001569 carbon dioxide Substances 0.000 claims abstract description 55
- 238000011084 recovery Methods 0.000 claims abstract description 36
- 125000005265 dialkylamine group Chemical group 0.000 claims abstract description 30
- 239000011877 solvent mixture Substances 0.000 claims abstract description 28
- 150000001298 alcohols Chemical class 0.000 claims abstract description 25
- 238000009835 boiling Methods 0.000 claims abstract description 22
- 230000000813 microbial effect Effects 0.000 claims abstract description 22
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 6
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 6
- 238000004821 distillation Methods 0.000 claims description 112
- 239000007789 gas Substances 0.000 claims description 85
- 241000894006 Bacteria Species 0.000 claims description 50
- 239000012071 phase Substances 0.000 claims description 47
- 239000001257 hydrogen Substances 0.000 claims description 45
- 229910052739 hydrogen Inorganic materials 0.000 claims description 45
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 43
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 43
- 235000015097 nutrients Nutrition 0.000 claims description 43
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 31
- 150000002431 hydrogen Chemical class 0.000 claims description 27
- 125000005270 trialkylamine group Chemical group 0.000 claims description 25
- 230000000789 acetogenic effect Effects 0.000 claims description 24
- 150000001412 amines Chemical class 0.000 claims description 24
- 239000007788 liquid Substances 0.000 claims description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 20
- 150000001408 amides Chemical class 0.000 claims description 20
- 238000000926 separation method Methods 0.000 claims description 20
- 230000001580 bacterial effect Effects 0.000 claims description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 12
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 241000186566 Clostridium ljungdahlii Species 0.000 claims description 9
- 238000005192 partition Methods 0.000 claims description 9
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 8
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 claims description 8
- 238000004064 recycling Methods 0.000 claims description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 6
- 238000000354 decomposition reaction Methods 0.000 claims description 5
- 239000012510 hollow fiber Substances 0.000 claims description 5
- 231100000053 low toxicity Toxicity 0.000 claims description 5
- 239000012528 membrane Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 claims description 4
- 241001464894 Blautia producta Species 0.000 claims description 3
- 241001656810 Clostridium aceticum Species 0.000 claims description 3
- 241000193401 Clostridium acetobutylicum Species 0.000 claims description 3
- 241000193161 Clostridium formicaceticum Species 0.000 claims description 3
- 241000186570 Clostridium kluyveri Species 0.000 claims description 3
- 241000186398 Eubacterium limosum Species 0.000 claims description 3
- 241000193459 Moorella thermoacetica Species 0.000 claims description 3
- 241000193448 Ruminiclostridium thermocellum Species 0.000 claims description 3
- 241000193446 Thermoanaerobacterium thermosaccharolyticum Species 0.000 claims description 3
- 229910052786 argon Inorganic materials 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000000284 extract Substances 0.000 claims description 3
- 229910052734 helium Inorganic materials 0.000 claims description 3
- 239000001307 helium Substances 0.000 claims description 3
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 3
- 241001468163 Acetobacterium woodii Species 0.000 claims description 2
- 241001137870 Thermoanaerobacterium Species 0.000 claims description 2
- 230000001476 alcoholic effect Effects 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000002609 medium Substances 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 238000012546 transfer Methods 0.000 claims description 2
- 239000003799 water insoluble solvent Substances 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims 1
- 238000010640 amide synthesis reaction Methods 0.000 abstract description 22
- 239000002253 acid Substances 0.000 description 40
- YOFPVMWVLDSWKR-UHFFFAOYSA-N 11-methyl-n-(11-methyldodecyl)dodecan-1-amine Chemical compound CC(C)CCCCCCCCCCNCCCCCCCCCCC(C)C YOFPVMWVLDSWKR-UHFFFAOYSA-N 0.000 description 24
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 18
- 239000000047 product Substances 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- 230000004048 modification Effects 0.000 description 12
- 238000012986 modification Methods 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 244000005700 microbiome Species 0.000 description 9
- 230000008901 benefit Effects 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000010525 oxidative degradation reaction Methods 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000011593 sulfur Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
- 230000001413 cellular effect Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000013459 approach Methods 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- PZFYOFFTIYJCEW-UHFFFAOYSA-N n-tridecyltridecan-1-amine Chemical compound CCCCCCCCCCCCCNCCCCCCCCCCCCC PZFYOFFTIYJCEW-UHFFFAOYSA-N 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 3
- 239000000052 vinegar Substances 0.000 description 3
- 235000021419 vinegar Nutrition 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 159000000021 acetate salts Chemical class 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000012263 liquid product Substances 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 239000012466 permeate Substances 0.000 description 2
- 238000011027 product recovery Methods 0.000 description 2
- 241001468161 Acetobacterium Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- -1 amide formate Chemical class 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001944 continuous distillation Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 235000020774 essential nutrients Nutrition 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000012092 media component Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- ZMBHCYHQLYEYDV-UHFFFAOYSA-N trioctylphosphine oxide Chemical compound CCCCCCCCP(=O)(CCCCCCCC)CCCCCCCC ZMBHCYHQLYEYDV-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/54—Acetic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/02—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C211/03—Monoamines
- C07C211/07—Monoamines containing one, two or three alkyl groups, each having the same number of carbon atoms in excess of three
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
- C07C51/44—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/47—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/48—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- General Chemical & Material Sciences (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Extraction Or Liquid Replacement (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9947598P | 1998-09-08 | 1998-09-08 | |
US9943998P | 1998-09-08 | 1998-09-08 | |
US9944098P | 1998-09-08 | 1998-09-08 | |
US9943898P | 1998-09-08 | 1998-09-08 | |
PCT/US1999/020416 WO2000014052A1 (en) | 1998-09-08 | 1999-09-07 | Microbial process for the preparation of acetic acid as well as solvent for its extraction from the fermentation broth |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20011161D0 NO20011161D0 (no) | 2001-03-07 |
NO20011161L NO20011161L (no) | 2001-04-25 |
NO326769B1 true NO326769B1 (no) | 2009-02-16 |
Family
ID=27493060
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20011161A NO326769B1 (no) | 1998-09-08 | 2001-03-07 | Blanding egnet for ekstrahering av eddiksyre fra en vandig strom, fremgangsmate for a oppna eddiksyre fra en vandig fase samt fermenteringsprosess for fremstilling av eddiksyre |
NO20082453A NO20082453L (no) | 1998-09-08 | 2008-05-30 | Mikrobiell prosess for fremstilling av eddiksyre, samt som opplosningsmiddel for dens ekstraksjon fra fermenteringsbuljongen |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20082453A NO20082453L (no) | 1998-09-08 | 2008-05-30 | Mikrobiell prosess for fremstilling av eddiksyre, samt som opplosningsmiddel for dens ekstraksjon fra fermenteringsbuljongen |
Country Status (26)
Country | Link |
---|---|
US (4) | USRE39175E1 (zh) |
EP (2) | EP1112246B1 (zh) |
JP (1) | JP4497724B2 (zh) |
KR (2) | KR100632773B1 (zh) |
CN (2) | CN1226273C (zh) |
AR (1) | AR023046A1 (zh) |
AT (1) | ATE286871T1 (zh) |
AU (1) | AU760956C (zh) |
BR (1) | BR9913527B1 (zh) |
CA (2) | CA2343231C (zh) |
CZ (2) | CZ303415B6 (zh) |
DE (1) | DE69923192T2 (zh) |
ES (1) | ES2237151T3 (zh) |
HK (1) | HK1040981B (zh) |
ID (1) | ID28710A (zh) |
MY (1) | MY154362A (zh) |
NO (2) | NO326769B1 (zh) |
NZ (3) | NZ535064A (zh) |
PL (2) | PL196768B1 (zh) |
PT (1) | PT1112246E (zh) |
RU (1) | RU2225445C2 (zh) |
TR (4) | TR200809539T2 (zh) |
TW (1) | TWI240717B (zh) |
UA (1) | UA72220C2 (zh) |
WO (1) | WO2000014052A1 (zh) |
ZA (1) | ZA200101560B (zh) |
Families Citing this family (196)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2275146C (en) | 1996-12-20 | 2006-10-31 | Usf Filtration And Separations Group, Inc. | Scouring method |
UA72220C2 (uk) | 1998-09-08 | 2005-02-15 | Байоенджініерінг Рісорсиз, Інк. | Незмішувана з водою суміш розчинник/співрозчинник для екстрагування оцтової кислоти, спосіб одержання оцтової кислоти (варіанти), спосіб анаеробного мікробного бродіння для одержання оцтової кислоти (варіанти), модифікований розчинник та спосіб його одержання |
US7074603B2 (en) | 1999-03-11 | 2006-07-11 | Zeachem, Inc. | Process for producing ethanol from corn dry milling |
ES2400285T3 (es) * | 1999-03-11 | 2013-04-08 | Zeachem, Inc. | Proceso para producir etanol |
AUPR421501A0 (en) | 2001-04-04 | 2001-05-03 | U.S. Filter Wastewater Group, Inc. | Potting method |
AUPR692401A0 (en) | 2001-08-09 | 2001-08-30 | U.S. Filter Wastewater Group, Inc. | Method of cleaning membrane modules |
AUPS300602A0 (en) | 2002-06-18 | 2002-07-11 | U.S. Filter Wastewater Group, Inc. | Methods of minimising the effect of integrity loss in hollow fibre membrane modules |
CA2501628C (en) | 2002-10-10 | 2012-12-04 | U.S. Filter Wastewater Group, Inc. | A filtration and backwashing arrangement for membrane modules |
AU2002953111A0 (en) | 2002-12-05 | 2002-12-19 | U. S. Filter Wastewater Group, Inc. | Mixing chamber |
CN1297529C (zh) * | 2003-05-15 | 2007-01-31 | 河北科技大学 | 丙酸菌发酵液的天然丙、乙酸酸化蒸馏提取法 |
CA2535360C (en) | 2003-08-29 | 2013-02-12 | U.S. Filter Wastewater Group, Inc. | Backwash |
AU2004289373B2 (en) | 2003-11-14 | 2010-07-29 | Evoqua Water Technologies Llc | Improved module cleaning method |
US6846431B1 (en) | 2003-12-26 | 2005-01-25 | Diversified Natural Products, Inc. | Environmentally benign, non-toxic, non-corrosive engine coolant/antifreeze |
MX306561B (es) * | 2004-01-29 | 2013-01-09 | Zeachem Inc | Recuperacion de acidos organicos. |
US8758621B2 (en) | 2004-03-26 | 2014-06-24 | Evoqua Water Technologies Llc | Process and apparatus for purifying impure water using microfiltration or ultrafiltration in combination with reverse osmosis |
JP2007535398A (ja) * | 2004-04-22 | 2007-12-06 | シーメンス ウォーター テクノロジース コーポレイション | 有機物質を消化するためのメンブレンバイオリアクタおよび処理槽を含む濾過装置ならびに廃液処理方法 |
NZ588094A (en) | 2004-08-20 | 2012-04-27 | Siemens Water Tech Corp | Potting head for hollow fibre filter module |
JP4838248B2 (ja) | 2004-09-07 | 2011-12-14 | シーメンス・ウォーター・テクノロジーズ・コーポレーション | 逆洗液体廃棄物の低減 |
US8506806B2 (en) | 2004-09-14 | 2013-08-13 | Siemens Industry, Inc. | Methods and apparatus for removing solids from a membrane module |
US8377305B2 (en) | 2004-09-15 | 2013-02-19 | Siemens Industry, Inc. | Continuously variable aeration |
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