FI57784C - Foerfarande foer separation av melass i socker och icke-sockersubstanser - Google Patents

Foerfarande foer separation av melass i socker och icke-sockersubstanser Download PDF

Info

Publication number: FI57784C
Authority: FI; Finland
Prior art keywords: sugar; vol; molasses; calcium; separation
Prior art date: 1973-12-14

Application number

FI3582/74A

Other languages

English (en)

Finnish (fi)

Other versions

FI57784B (fi

FI358274A7 (fr

Inventor

Mohammad Munir

Hubert Schiweck

Hans-Werner Weinz

Fritz Wurm

Original Assignee

Sueddeutsche Zucker Ag

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.)

1973-12-14

Filing date

1974-12-12

Publication date

1980-10-10

1974-12-12 Application filed by Sueddeutsche Zucker Ag filed Critical Sueddeutsche Zucker Ag

1975-06-15 Publication of FI358274A7 publication Critical patent/FI358274A7/fi

1980-06-30 Publication of FI57784B publication Critical patent/FI57784B/fi

1980-10-10 Application granted granted Critical

1980-10-10 Publication of FI57784C publication Critical patent/FI57784C/fi

Links

238000000926 separation method Methods 0.000 title claims description 14
235000000346 sugar Nutrition 0.000 claims description 57
235000013379 molasses Nutrition 0.000 claims description 35
238000000034 method Methods 0.000 claims description 20
150000001768 cations Chemical class 0.000 claims description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
238000005342 ion exchange Methods 0.000 claims description 9
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 6
239000000126 substance Substances 0.000 claims description 6
150000008163 sugars Chemical class 0.000 claims description 6
238000004811 liquid chromatography Methods 0.000 claims description 2
125000000542 sulfonic acid group Chemical group 0.000 claims description 2
159000000007 calcium salts Chemical class 0.000 claims 2
238000005341 cation exchange Methods 0.000 claims 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 9
238000010828 elution Methods 0.000 description 9
239000011575 calcium Substances 0.000 description 7
150000001875 compounds Chemical class 0.000 description 6
230000003068 static effect Effects 0.000 description 6
229920002554 vinyl polymer Polymers 0.000 description 6
NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 5
229910052791 calcium Inorganic materials 0.000 description 5
BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 4
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
229910001413 alkali metal ion Inorganic materials 0.000 description 4
239000003456 ion exchange resin Substances 0.000 description 4
229920003303 ion-exchange polymer Polymers 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229910001424 calcium ion Inorganic materials 0.000 description 3
239000003729 cation exchange resin Substances 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
WVAFEFUPWRPQSY-UHFFFAOYSA-N 1,2,3-tris(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1C=C WVAFEFUPWRPQSY-UHFFFAOYSA-N 0.000 description 2
SGVYKUFIHHTIFL-UHFFFAOYSA-N 2-methylnonane Chemical compound CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 2
KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 2
KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical class C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
239000003513 alkali Substances 0.000 description 2
229940023913 cation exchange resins Drugs 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
239000000975 dye Substances 0.000 description 2
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 2
229910001425 magnesium ion Inorganic materials 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
230000008929 regeneration Effects 0.000 description 2
238000011069 regeneration method Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000003860 storage Methods 0.000 description 2
UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical compound C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 0.000 description 2
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
NWRZGFYWENINNX-UHFFFAOYSA-N 1,1,2-tris(ethenyl)cyclohexane Chemical compound C=CC1CCCCC1(C=C)C=C NWRZGFYWENINNX-UHFFFAOYSA-N 0.000 description 1
QLLUAUADIMPKIH-UHFFFAOYSA-N 1,2-bis(ethenyl)naphthalene Chemical compound C1=CC=CC2=C(C=C)C(C=C)=CC=C21 QLLUAUADIMPKIH-UHFFFAOYSA-N 0.000 description 1
FCMUPMSEVHVOSE-UHFFFAOYSA-N 2,3-bis(ethenyl)pyridine Chemical compound C=CC1=CC=CN=C1C=C FCMUPMSEVHVOSE-UHFFFAOYSA-N 0.000 description 1
TURITJIWSQEMDB-UHFFFAOYSA-N 2-methyl-n-[(2-methylprop-2-enoylamino)methyl]prop-2-enamide Chemical compound CC(=C)C(=O)NCNC(=O)C(C)=C TURITJIWSQEMDB-UHFFFAOYSA-N 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
239000004641 Diallyl-phthalate Substances 0.000 description 1
229930091371 Fructose Natural products 0.000 description 1
239000005715 Fructose Substances 0.000 description 1
RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
241001441728 Molidae Species 0.000 description 1
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
MUPFEKGTMRGPLJ-RMMQSMQOSA-N Raffinose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 MUPFEKGTMRGPLJ-RMMQSMQOSA-N 0.000 description 1
240000000111 Saccharum officinarum Species 0.000 description 1
235000007201 Saccharum officinarum Nutrition 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
MUPFEKGTMRGPLJ-UHFFFAOYSA-N UNPD196149 Natural products OC1C(O)C(CO)OC1(CO)OC1C(O)C(O)C(O)C(COC2C(C(O)C(O)C(CO)O2)O)O1 MUPFEKGTMRGPLJ-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
235000016127 added sugars Nutrition 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
229960003237 betaine Drugs 0.000 description 1
ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
VPPSHXIFIAJKMX-UHFFFAOYSA-N bis(prop-2-enyl) 2,3-dihydroxybutanedioate Chemical compound C=CCOC(=O)C(O)C(O)C(=O)OCC=C VPPSHXIFIAJKMX-UHFFFAOYSA-N 0.000 description 1
QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
125000005586 carbonic acid group Chemical group 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000013375 chromatographic separation Methods 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
FNMTVMWFISHPEV-AATRIKPKSA-N dipropan-2-yl (e)-but-2-enedioate Chemical compound CC(C)OC(=O)\C=C\C(=O)OC(C)C FNMTVMWFISHPEV-AATRIKPKSA-N 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
235000011389 fruit/vegetable juice Nutrition 0.000 description 1
239000008103 glucose Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
229910052500 inorganic mineral Chemical class 0.000 description 1
229960004903 invert sugar Drugs 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000011707 mineral Chemical class 0.000 description 1
239000000203 mixture Substances 0.000 description 1
239000000178 monomer Substances 0.000 description 1
150000002772 monosaccharides Chemical class 0.000 description 1
AYGYHGXUJBFUJU-UHFFFAOYSA-N n-[2-(prop-2-enoylamino)ethyl]prop-2-enamide Chemical compound C=CC(=O)NCCNC(=O)C=C AYGYHGXUJBFUJU-UHFFFAOYSA-N 0.000 description 1
LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
238000005192 partition Methods 0.000 description 1
230000035515 penetration Effects 0.000 description 1
DBSDMAPJGHBWAL-UHFFFAOYSA-N penta-1,4-dien-3-ylbenzene Chemical compound C=CC(C=C)C1=CC=CC=C1 DBSDMAPJGHBWAL-UHFFFAOYSA-N 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
230000035939 shock Effects 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
125000001174 sulfone group Chemical group 0.000 description 1
XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
239000001993 wax Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13B—PRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
- C13B35/00—Extraction of sucrose from molasses
- C13B35/02—Extraction of sucrose from molasses by chemical means
- C13B35/06—Extraction of sucrose from molasses by chemical means using ion exchange

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
Organic Chemistry (AREA)
Saccharide Compounds (AREA)
Treatment Of Liquids With Adsorbents In General (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

FI3582/74A 1973-12-14 1974-12-12 Foerfarande foer separation av melass i socker och icke-sockersubstanser FI57784C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE2362211		1973-12-14
DE2362211A DE2362211C3 (de)	1973-12-14	1973-12-14	Verfahren zur Aufarbeitung von Melassen

Publications (3)

Publication Number	Publication Date
FI358274A7 FI358274A7 (fr)	1975-06-15
FI57784B FI57784B (fi)	1980-06-30
FI57784C true FI57784C (fi)	1980-10-10

Family

ID=5900770

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI3582/74A FI57784C (fi)	1973-12-14	1974-12-12	Foerfarande foer separation av melass i socker och icke-sockersubstanser

Country Status (26)

Country	Link
US (1)	US3975205A (fr)
JP (1)	JPS5719959B2 (fr)
AR (1)	AR201795A1 (fr)
AT (1)	AT337122B (fr)
BE (1)	BE823320A (fr)
BG (1)	BG26203A3 (fr)
CH (1)	CH606439A5 (fr)
DD (1)	DD116633A5 (fr)
DE (1)	DE2362211C3 (fr)
DK (1)	DK652674A (fr)
ES (1)	ES432902A1 (fr)
FI (1)	FI57784C (fr)
FR (1)	FR2272174B1 (fr)
GB (1)	GB1448524A (fr)
HU (1)	HU170337B (fr)
IE (1)	IE40300B1 (fr)
IN (1)	IN140210B (fr)
IT (1)	IT1024418B (fr)
NL (1)	NL7416136A (fr)
PH (1)	PH11729A (fr)
PL (1)	PL101202B1 (fr)
RO (1)	RO76618A (fr)
SE (1)	SE7415619L (fr)
SU (1)	SU549088A3 (fr)
TR (1)	TR18440A (fr)
ZA (1)	ZA747957B (fr)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4046590A (en) *	1976-09-08	1977-09-06	California And Hawaiian Sugar Company	Process for the production of a colorless sugar syrup from cane molasses
DE2735995C2 (de) *	1977-08-10	1982-06-09	Gerhard Dipl.-Chem. Dr.rer.nat. 4040 Neuss Quentin	Verfahren zur Reinigung technischer Zuckerlösungen
AU540231B2 (en) *	1978-11-02	1984-11-08	Mitsubishi Kasei Corporation	Adsorption separation method and apparatus
NL7909337A (nl) *	1979-12-28	1981-07-16	Akzo Nv	Werkwijze voor de regeneratie van sorbentia, in het bijzonder ionenuitwisselaars.
GR73024B (fr) *	1980-02-29	1984-01-25	Suomen Sokeri Oy
JPS61295540A (ja) *	1985-06-24	1986-12-26	Konishiroku Photo Ind Co Ltd	自動焦点式のカラ−プリンタ
DE3630878C1 (en) *	1986-09-11	1988-03-10	Amino Gmbh	Process for the preparation of L-tryptophan and DL-serine
JPH01238939A (ja) *	1988-03-18	1989-09-25	Fuji Photo Film Co Ltd	画像記録装置
FI86416C (fi) *	1988-06-09	1992-08-25	Suomen Sokeri Oy	Foerfarande foer tillvaratagande av betain ur melass.
US6663780B2 (en)	1993-01-26	2003-12-16	Danisco Finland Oy	Method for the fractionation of molasses
FI96225C (fi)	1993-01-26	1996-05-27	Cultor Oy	Menetelmä melassin fraktioimiseksi
US5443650B2 (en) *	1993-06-11	2000-05-30	Univ Louisiana State	Process for softening a sugar-containing aqueous solution such as sugar juice or molasses
US5466294A (en) *	1993-12-14	1995-11-14	The Amalgamated Sugar Company	Sugar beet juice purification process
US5795398A (en)	1994-09-30	1998-08-18	Cultor Ltd.	Fractionation method of sucrose-containing solutions
US6224776B1 (en)	1996-05-24	2001-05-01	Cultor Corporation	Method for fractionating a solution
JP3539470B2 (ja) *	1997-12-25	2004-07-07	オルガノ株式会社	ベタインの回収方法
FI20002150L (fi) *	2000-09-29	2002-03-30	Finnfeeds Finland Oy	Menetelmä tuotteiden talteenottamiseksi prosessiliuoksista
FI20010977A7 (fi)	2001-05-09	2002-11-10	Danisco Sweeteners Oy	Kromatografinen erotusmenetelmä
FI20021251A0 (fi)	2002-06-26	2002-06-26	Finnfeeds Finland Oy	Menetelmä betaiinin talteenottamiseksi
EP1781116A4 (fr) *	2004-06-04	2009-07-29	Horizon Science Pty Ltd	Edulcorant naturel
CN101203270B (zh)	2005-06-03	2014-07-02	视界科技有限公司	具有体重再分配性能的物质
CN104323268A (zh) *	2006-09-19	2015-02-04	视界科技有限公司	从甘蔗中获得的提取物及其生产方法
CN103561585B (zh)	2011-02-08	2016-05-25	产品制造者(澳大利亚)有限公司	糖提取物
MY171216A (en)	2012-08-28	2019-10-02	The Product Makers Australia Pty Ltd	Extraction method
EP3035949B1 (fr)	2013-08-16	2023-10-04	Poly Gain Pte Ltd	Extraits dérivés de canne à sucre et utilisations
RU2765487C1 (ru) *	2020-10-01	2022-01-31	Федеральное государственное бюджетное образовательное учреждение высшего образования "Кубанский государственный технологический университет" (ФГБОУ ВО "КубГТУ")	Способ получения бетаина и сахарозы из мелассы
CN113319110B (zh) *	2021-05-18	2023-01-24	昆明理工大学	一种酒精废醪液喷淋修复重金属污染土壤及增肥的方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2868677A (en) *	1956-07-30	1959-01-13	Ultra Sucro Company	Clarification and demineralization process for b-molasses and similar materials containing concentrated impurities
US2971868A (en) *	1958-05-02	1961-02-14	Rohm & Haas	Ion exchange process
US2929746A (en) *	1959-06-02	1960-03-22	Rohm & Haas	Process for purifying sugar
DE1567248A1 (de) *	1966-08-25	1970-06-25	Braunschweigische Maschb Ansta	Verfahren zur Gewinnung von Fluessigzucker hoher Reinheit aus Rohrmelassen
US3785864A (en) *	1970-07-23	1974-01-15	Boehringer Mannheim Gmbh	Process for the chromatographic separation of multi-component mixtures containing glucose
US3767526A (en) *	1971-12-06	1973-10-23	Agency Ind Science Techn	Method for increasing yield of sucrose

1973
- 1973-12-14 DE DE2362211A patent/DE2362211C3/de not_active Expired
1974
- 1974-11-27 US US05/527,799 patent/US3975205A/en not_active Expired - Lifetime
- 1974-12-03 AR AR256762A patent/AR201795A1/es active
- 1974-12-05 IN IN2693/CAL/74A patent/IN140210B/en unknown
- 1974-12-06 HU HUSU882A patent/HU170337B/hu unknown
- 1974-12-09 BG BG028404A patent/BG26203A3/xx unknown
- 1974-12-10 PH PH16606A patent/PH11729A/en unknown
- 1974-12-11 RO RO7480758A patent/RO76618A/fr unknown
- 1974-12-11 SU SU2083397A patent/SU549088A3/ru active
- 1974-12-11 NL NL7416136A patent/NL7416136A/xx not_active Application Discontinuation
- 1974-12-11 IT IT54493/74A patent/IT1024418B/it active
- 1974-12-11 DD DD182931A patent/DD116633A5/xx unknown
- 1974-12-11 JP JP14164174A patent/JPS5719959B2/ja not_active Expired
- 1974-12-12 SE SE7415619A patent/SE7415619L/xx unknown
- 1974-12-12 IE IE2556/74A patent/IE40300B1/xx unknown
- 1974-12-12 PL PL1974176410A patent/PL101202B1/pl unknown
- 1974-12-12 GB GB5375074A patent/GB1448524A/en not_active Expired
- 1974-12-12 TR TR18440A patent/TR18440A/xx unknown
- 1974-12-12 AT AT991474A patent/AT337122B/de not_active IP Right Cessation
- 1974-12-12 FI FI3582/74A patent/FI57784C/fi active
- 1974-12-13 ES ES432902A patent/ES432902A1/es not_active Expired
- 1974-12-13 FR FR7441227A patent/FR2272174B1/fr not_active Expired
- 1974-12-13 CH CH1663274A patent/CH606439A5/xx not_active IP Right Cessation
- 1974-12-13 BE BE151475A patent/BE823320A/fr not_active IP Right Cessation
- 1974-12-13 ZA ZA00747957A patent/ZA747957B/xx unknown
- 1974-12-13 DK DK652674A patent/DK652674A/da unknown

Also Published As

Publication number	Publication date
IT1024418B (it)	1978-06-20
RO76618A (fr)	1981-04-30
GB1448524A (en)	1976-09-08
BE823320A (fr)	1975-06-13
ZA747957B (en)	1976-01-28
DD116633A5 (fr)	1975-12-05
ATA991474A (de)	1976-09-15
BG26203A3 (bg)	1979-02-15
AU7625074A (en)	1976-06-10
FI57784B (fi)	1980-06-30
CH606439A5 (fr)	1978-10-31
PH11729A (en)	1978-05-30
FR2272174A1 (fr)	1975-12-19
ES432902A1 (es)	1976-11-01
AR201795A1 (es)	1975-04-15
SE7415619L (fr)	1975-06-16
FI358274A7 (fr)	1975-06-15
SU549088A3 (ru)	1977-02-28
AT337122B (de)	1977-06-10
NL7416136A (nl)	1975-06-17
JPS5094145A (fr)	1975-07-26
IE40300L (en)	1975-06-14
DE2362211B2 (de)	1976-01-22
US3975205A (en)	1976-08-17
DK652674A (fr)	1975-08-18
IE40300B1 (en)	1979-04-25
PL101202B1 (pl)	1978-12-30
FR2272174B1 (fr)	1980-02-22
DE2362211C3 (de)	1978-05-11
IN140210B (fr)	1976-09-25
HU170337B (fr)	1977-05-28
DE2362211A1 (de)	1975-06-19
JPS5719959B2 (fr)	1982-04-26
TR18440A (tr)	1977-02-16

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EP1490521B1 (fr)	2013-12-11	Separation de sucres, d'alcools de sucres, d'hydrates de carbone et de melanges de ceux-ci
CN102946961B (zh)	2015-11-25	分离方法
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US5127957A (en)	1992-07-07	Method for the recovery of betaine from molasses
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CN118076423A (zh)	2024-05-24	混合离子形式糖色谱法
JPS60130400A (ja)	1985-07-11	イオン交換樹脂による糖類の分離、精製方法