FI61519C - Foerfarande och apparatur foer framstaellning av modifierade staerkelseprodukter - Google Patents

Foerfarande och apparatur foer framstaellning av modifierade staerkelseprodukter Download PDF

Info

Publication number: FI61519C
Authority: FI; Finland
Prior art keywords: zone; starch; reaction; heating; slurry
Prior art date: 1975-06-10

Application number

FI761671A

Other languages

English (en)

Finnish (fi)

Swedish (sv)

Other versions

FI761671A7 (fr

FI61519B (fi

Inventor

John F Hughes

Original Assignee

Cellcor Corp Of Canada Ltd

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.)

1975-06-10

Filing date

1976-06-10

Publication date

1982-08-10

1976-06-10 Application filed by Cellcor Corp Of Canada Ltd filed Critical Cellcor Corp Of Canada Ltd

1976-12-11 Publication of FI761671A7 publication Critical patent/FI761671A7/fi

1982-04-30 Application granted granted Critical

1982-04-30 Publication of FI61519B publication Critical patent/FI61519B/fi

1982-08-10 Publication of FI61519C publication Critical patent/FI61519C/fi

Links

229920002472 Starch Polymers 0.000 claims description 106
235000019698 starch Nutrition 0.000 claims description 106
239000008107 starch Substances 0.000 claims description 101
239000002002 slurry Substances 0.000 claims description 46
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 45
238000006243 chemical reaction Methods 0.000 claims description 41
239000000463 material Substances 0.000 claims description 31
238000000034 method Methods 0.000 claims description 28
239000004202 carbamide Substances 0.000 claims description 23
238000010438 heat treatment Methods 0.000 claims description 19
230000008569 process Effects 0.000 claims description 18
239000007788 liquid Substances 0.000 claims description 17
150000001875 compounds Chemical class 0.000 claims description 11
229920000881 Modified starch Polymers 0.000 claims description 8
239000004368 Modified starch Substances 0.000 claims description 8
238000004519 manufacturing process Methods 0.000 claims description 8
235000019426 modified starch Nutrition 0.000 claims description 8
150000007519 polyprotic acids Polymers 0.000 claims description 7
150000005846 sugar alcohols Polymers 0.000 claims description 7
150000001412 amines Chemical class 0.000 claims description 6
230000015572 biosynthetic process Effects 0.000 claims description 4
150000007524 organic acids Chemical class 0.000 claims description 4
239000007921 spray Substances 0.000 claims description 4
150000008064 anhydrides Chemical class 0.000 claims description 3
150000007522 mineralic acids Chemical class 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
238000005086 pumping Methods 0.000 claims description 3
150000001408 amides Chemical class 0.000 claims description 2
239000003595 mist Substances 0.000 claims description 2
238000005979 thermal decomposition reaction Methods 0.000 claims 1
239000000047 product Substances 0.000 description 27
229920005862 polyol Polymers 0.000 description 24
150000003077 polyols Chemical class 0.000 description 24
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
239000002253 acid Substances 0.000 description 12
229920002261 Corn starch Polymers 0.000 description 9
239000008120 corn starch Substances 0.000 description 9
229910052740 iodine Inorganic materials 0.000 description 9
239000011630 iodine Substances 0.000 description 9
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 8
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 8
239000000543 intermediate Substances 0.000 description 8
239000010802 sludge Substances 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
239000012530 fluid Substances 0.000 description 6
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 6
229920002635 polyurethane Polymers 0.000 description 6
239000004814 polyurethane Substances 0.000 description 6
239000007787 solid Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
229910001220 stainless steel Inorganic materials 0.000 description 6
239000010935 stainless steel Substances 0.000 description 6
238000012360 testing method Methods 0.000 description 6
244000061456 Solanum tuberosum Species 0.000 description 5
235000002595 Solanum tuberosum Nutrition 0.000 description 5
239000000853 adhesive Substances 0.000 description 5
230000001070 adhesive effect Effects 0.000 description 5
229920000180 alkyd Polymers 0.000 description 5
239000001257 hydrogen Substances 0.000 description 5
229910052739 hydrogen Inorganic materials 0.000 description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
229920000642 polymer Polymers 0.000 description 5
230000009257 reactivity Effects 0.000 description 5
229920000856 Amylose Polymers 0.000 description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
-1 aliphatic amines Chemical class 0.000 description 4
238000010411 cooking Methods 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
230000000694 effects Effects 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
239000000499 gel Substances 0.000 description 4
229910052500 inorganic mineral Inorganic materials 0.000 description 4
239000011707 mineral Substances 0.000 description 4
238000012545 processing Methods 0.000 description 4
239000002699 waste material Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
230000008901 benefit Effects 0.000 description 3
239000003153 chemical reaction reagent Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000002845 discoloration Methods 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000012948 isocyanate Substances 0.000 description 3
150000002513 isocyanates Chemical class 0.000 description 3
239000003921 oil Substances 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
239000003973 paint Substances 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
239000002994 raw material Substances 0.000 description 3
238000010186 staining Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
229920000945 Amylopectin Polymers 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
230000008859 change Effects 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
239000008199 coating composition Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
238000001035 drying Methods 0.000 description 2
238000005485 electric heating Methods 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
238000003475 lamination Methods 0.000 description 2
239000000203 mixture Substances 0.000 description 2
239000003607 modifier Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000004033 plastic Substances 0.000 description 2
235000012015 potatoes Nutrition 0.000 description 2
239000000843 powder Substances 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
230000009467 reduction Effects 0.000 description 2
238000010517 secondary reaction Methods 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000004753 textile Substances 0.000 description 2
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
238000004073 vulcanization Methods 0.000 description 2
ITMIRWIISVVMAK-UHFFFAOYSA-N 2-chloro-3-ethyloxirane Chemical class CCC1OC1Cl ITMIRWIISVVMAK-UHFFFAOYSA-N 0.000 description 1
SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
KPYCVQASEGGKEG-UHFFFAOYSA-N 3-hydroxyoxolane-2,5-dione Chemical compound OC1CC(=O)OC1=O KPYCVQASEGGKEG-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
239000004606 Fillers/Extenders Substances 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
240000003183 Manihot esculenta Species 0.000 description 1
235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
230000004913 activation Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000003974 aralkylamines Chemical class 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
238000010923 batch production Methods 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
150000001869 cobalt compounds Chemical class 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
239000002178 crystalline material Substances 0.000 description 1
230000003413 degradative effect Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000000835 fiber Substances 0.000 description 1
125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
239000008187 granular material Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000003944 halohydrins Chemical class 0.000 description 1
229920006158 high molecular weight polymer Polymers 0.000 description 1
239000011346 highly viscous material Substances 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
235000021374 legumes Nutrition 0.000 description 1
235000021388 linseed oil Nutrition 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
230000013011 mating Effects 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
150000003214 pyranose derivatives Chemical group 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
125000006850 spacer group Chemical group 0.000 description 1
230000008961 swelling Effects 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
239000010409 thin film Substances 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000011345 viscous material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B30/00—Preparation of starch, degraded or non-chemically modified starch, amylose, or amylopectin
- C08B30/12—Degraded, destructured or non-chemically modified starch, e.g. mechanically, enzymatically or by irradiation; Bleaching of starch
- C08B30/16—Apparatus therefor
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
- C08L3/02—Starch; Degradation products thereof, e.g. dextrin
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J103/00—Adhesives based on starch, amylose or amylopectin or on their derivatives or degradation products
- C09J103/02—Starch; Degradation products thereof, e.g. dextrin

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Engineering & Computer Science (AREA)
Biochemistry (AREA)
Materials Engineering (AREA)
Life Sciences & Earth Sciences (AREA)
Crystallography & Structural Chemistry (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)
Adhesives Or Adhesive Processes (AREA)
Paper (AREA)

FI761671A 1975-06-10 1976-06-10 Foerfarande och apparatur foer framstaellning av modifierade staerkelseprodukter FI61519C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US58581075A	1975-06-10	1975-06-10
US58581075		1975-06-10

Publications (3)

Publication Number	Publication Date
FI761671A7 FI761671A7 (fr)	1976-12-11
FI61519B FI61519B (fi)	1982-04-30
FI61519C true FI61519C (fi)	1982-08-10

Family

ID=24343057

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI761671A FI61519C (fi)	1975-06-10	1976-06-10	Foerfarande och apparatur foer framstaellning av modifierade staerkelseprodukter

Country Status (16)

Country	Link
US (1)	US4155884A (fr)
JP (1)	JPS51151345A (fr)
AU (1)	AU498436B2 (fr)
BE (2)	BE842704A (fr)
BR (1)	BR7603642A (fr)
CA (1)	CA1067898A (fr)
DE (1)	DE2626110C2 (fr)
ES (1)	ES448652A1 (fr)
FI (1)	FI61519C (fr)
FR (1)	FR2314253A1 (fr)
GB (1)	GB1528851A (fr)
IT (1)	IT1063595B (fr)
NL (1)	NL7606212A (fr)
NO (1)	NO142842C (fr)
SE (1)	SE434756B (fr)
ZA (1)	ZA763423B (fr)

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US4242241A (en) *	1977-10-31	1980-12-30	The Celotex Corporation	Method for making a slurry containing particulate matter and fibers for a preformed insulation product
FR2411236A1 (fr) *	1977-12-08	1979-07-06	Cellcor Corp Of Canada Ltd	Procede de preparation d'hydrolysats d'amidon
SE452327B (sv) *	1979-08-28	1987-11-23	St Lawrence Tech Ltd	Kemisk reaktor for framstellning av modifierad sterkelse och sterkelsederivat i homogen flytande form
US4321364A (en) *	1980-04-17	1982-03-23	Minister For Public Works For The State Of New South Wales	Preparation of soluble chromogenic substrates
US4391836A (en) *	1980-08-08	1983-07-05	National Starch And Chemical Corporation	Process for preparing instant gelling starches
US4505757A (en) *	1982-02-16	1985-03-19	Kaken Pharmaceutical Co. Ltd.	Method for a specific depolymerization of a polysaccharide having a rod-like helical conformation
US4578353A (en) *	1982-07-19	1986-03-25	St. Lawrence Reactors Limited	Fermentation of glucose with recycle of non-fermented components
US4497896A (en) *	1982-07-19	1985-02-05	St. Lawrence Technologies Limited	Fermentation of glucose with recycle of non-fermented components
US4667654A (en) *	1985-07-10	1987-05-26	National Starch And Chemical Corporation	Pulse combustion process for the preparation of pregelatinized starches
US4761185A (en) *	1986-11-14	1988-08-02	Universite De Sherbrooke	Rapid starch depolymerization via spray reactors
FR2647050B1 (fr) *	1989-05-16	1991-11-22	Seppic Sa	Procede de fabrication d'un amidon directement compressible en vue de l'utilisation dans la fabrication de comprimes et comprimes obtenus
US5032683A (en) *	1989-06-26	1991-07-16	Sequa Chemicals, Inc.	Glyoxal modified aqueous starch dispersion and method
DE3931363A1 (de) *	1989-09-20	1991-03-28	Tomka Ivan	Verfahren zur reduktion der quellbarkeit von staerke
DE69229710T2 (de) *	1991-11-15	2000-03-02	Kanegafuchi Kagaku Kogyo K.K., Osaka	Esterbindung enthaltende Polymere für pharmazeutische Zubereitungen
US5320669A (en) *	1992-12-14	1994-06-14	Iowa State University Research Foundation, Inc.	Cereal grain-based biodegradable thermoplastic compositions
NL9300214A (nl) *	1993-02-03	1994-09-01	Avebe Coop Verkoop Prod	Werkwijze voor het bereiden van een smeltkleefstofsamenstelling alsmede voorwerpen die onder toepassing van een dergelijke samenstelling zijn vervaardigd.
US5525154A (en) *	1994-11-04	1996-06-11	Universite Laval	Method for the hydrolysis of starchy materials by sweetpotato endogenous amylases
FR2850391B1 (fr) *	2003-01-24	2007-04-20	Roquette Freres	Procede et composition adhesive aqueuse pour la production de panneaux a base de matieres vegetales
DE10325535B4 (de) *	2003-06-04	2007-02-22	Mühle Rüningen GmbH & Co. KG	Papierleimungsmittel und Verfahren zu dessen Herstellung sowie dessen Verwendung
US8057621B2 (en) *	2005-04-12	2011-11-15	Kohler Herbert B	Apparatus and method for producing a corrugated product under ambient temperature conditions
US7815741B2 (en)	2006-11-03	2010-10-19	Olson David A	Reactor pump for catalyzed hydrolytic splitting of cellulose
US7815876B2 (en)	2006-11-03	2010-10-19	Olson David A	Reactor pump for catalyzed hydrolytic splitting of cellulose
WO2008157705A1 (fr) *	2007-06-20	2008-12-24	Kohler Herbert B	Procédé de production de carton ondulé
EP3508339B1 (fr)	2008-03-21	2023-11-15	International Paper Company	Procédé de production de carton ondulé
EP2391505B1 (fr) *	2009-01-22	2021-03-10	Intpro, Llc	Procédé de contrôle de l'humidité et de la température lors d'une opération d'ondulation
CN102766422B (zh) *	2012-05-16	2014-03-05	桐乡嘉力丰实业股份有限公司	一种糯米湿胶及其制备方法
EP3251826B1 (fr)	2012-11-01	2020-07-22	HBK Family, LLC	Procédé pour rainurer une bande dans le sens de la machine
DE102017127632A1 (de) *	2017-11-22	2019-05-23	Bauer Verfahrenstechnik Gmbh	Verfahren zur kontinuierlichen thermischen Behandlung eines wässrigen Stärkezustands
CN114206601B (zh)	2019-08-05	2023-06-09	因特普罗有限责任公司	行进纸幅材中特定于纸的水分控制
CN111772173A (zh) *	2020-08-19	2020-10-16	佛山高峰淀粉科技有限公司	一种马蹄糕用变性淀粉及其制备工艺

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2735792A (en) *		1956-02-21		kroyer
US2417969A (en) *	1941-12-15	1947-03-25	Stein Hall & Co Inc	Dissociated starch and method of making the same
BE615950A (fr) *	1961-04-03
GB1008042A (en) *	1962-11-27	1965-10-22	Corn Products Co	Process for modifying a carbohydrate material
CA941825A (en) *	1970-07-14	1974-02-12	Scholten-Honig Research N. V.	Redispersible hydrophobic starch derivatives and process for their preparation

1976
- 1976-06-08 GB GB23535/76A patent/GB1528851A/en not_active Expired
- 1976-06-08 ES ES448652A patent/ES448652A1/es not_active Expired
- 1976-06-08 BE BE167722A patent/BE842704A/fr not_active IP Right Cessation
- 1976-06-08 AU AU14710/76A patent/AU498436B2/en not_active Expired
- 1976-06-08 BR BR3642/76A patent/BR7603642A/pt unknown
- 1976-06-08 BE BE942704A patent/BE942704A/fr unknown
- 1976-06-09 ZA ZA763423A patent/ZA763423B/xx unknown
- 1976-06-09 SE SE7606495A patent/SE434756B/xx not_active IP Right Cessation
- 1976-06-09 FR FR7617338A patent/FR2314253A1/fr active Granted
- 1976-06-09 NL NL7606212A patent/NL7606212A/xx not_active Application Discontinuation
- 1976-06-09 NO NO761960A patent/NO142842C/no unknown
- 1976-06-09 IT IT24118/76A patent/IT1063595B/it active
- 1976-06-10 FI FI761671A patent/FI61519C/fi not_active IP Right Cessation
- 1976-06-10 JP JP51068609A patent/JPS51151345A/ja active Granted
- 1976-06-10 DE DE2626110A patent/DE2626110C2/de not_active Expired
- 1976-06-10 CA CA254,545A patent/CA1067898A/fr not_active Expired
1978
- 1978-01-25 US US05/872,237 patent/US4155884A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
IT1063595B (it)	1985-02-11
GB1528851A (en)	1978-10-18
NL7606212A (nl)	1976-12-14
NO761960L (fr)	1976-12-13
JPS51151345A (en)	1976-12-25
SE434756B (sv)	1984-08-13
NO142842B (no)	1980-07-21
BE942704A (fr)	1976-10-01
FR2314253B1 (fr)	1981-05-22
BR7603642A (pt)	1977-01-25
DE2626110A1 (de)	1976-12-30
FI761671A7 (fr)	1976-12-11
BE842704A (fr)	1976-10-01
FR2314253A1 (fr)	1977-01-07
FI61519B (fi)	1982-04-30
AU1471076A (en)	1977-12-15
DE2626110C2 (de)	1987-03-26
ES448652A1 (es)	1977-12-01
JPS5754120B2 (fr)	1982-11-16
US4155884A (en)	1979-05-22
AU498436B2 (en)	1979-03-15
CA1067898A (fr)	1979-12-11
NO142842C (no)	1980-10-29
ZA763423B (en)	1977-05-25
SE7606495L (sv)	1976-12-11

Legal Events

Date	Code	Title	Description
2004-08-31	MM	Patent lapsed	Owner name: CELLCOR CORPORATION OF CANADA LIMITED

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