DE1617908A1 - Grundlage fuer Kaugummi - Google Patents
Grundlage fuer KaugummiInfo
- Publication number
- DE1617908A1 DE1617908A1 DE19661617908 DE1617908A DE1617908A1 DE 1617908 A1 DE1617908 A1 DE 1617908A1 DE 19661617908 DE19661617908 DE 19661617908 DE 1617908 A DE1617908 A DE 1617908A DE 1617908 A1 DE1617908 A1 DE 1617908A1
- Authority
- DE
- Germany
- Prior art keywords
- polymer
- weight
- chewing gum
- ethylene
- base
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 235000015218 chewing gum Nutrition 0.000 title claims description 37
- 229940112822 chewing gum Drugs 0.000 title claims description 35
- 229920000642 polymer Polymers 0.000 claims description 46
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 34
- 239000005977 Ethylene Substances 0.000 claims description 34
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 28
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical group CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 claims description 8
- 229920001567 vinyl ester resin Polymers 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 20
- 229920001577 copolymer Polymers 0.000 description 19
- 239000000203 mixture Substances 0.000 description 19
- 239000000178 monomer Substances 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 15
- 229920002689 polyvinyl acetate Polymers 0.000 description 13
- 239000011118 polyvinyl acetate Substances 0.000 description 13
- 239000007787 solid Substances 0.000 description 11
- 230000001055 chewing effect Effects 0.000 description 8
- 230000036571 hydration Effects 0.000 description 8
- 238000006703 hydration reaction Methods 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 229920001897 terpolymer Polymers 0.000 description 8
- 229920001206 natural gum Polymers 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 229920001412 Chicle Polymers 0.000 description 6
- 240000001794 Manilkara zapota Species 0.000 description 6
- 235000011339 Manilkara zapota Nutrition 0.000 description 6
- 229930006000 Sucrose Natural products 0.000 description 6
- 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 6
- 240000008042 Zea mays Species 0.000 description 6
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 6
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 6
- 235000005822 corn Nutrition 0.000 description 6
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 229960004793 sucrose Drugs 0.000 description 6
- 239000006188 syrup Substances 0.000 description 6
- 235000020357 syrup Nutrition 0.000 description 6
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 5
- 229920001038 ethylene copolymer Polymers 0.000 description 5
- 150000001451 organic peroxides Chemical class 0.000 description 5
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 4
- 235000019477 peppermint oil Nutrition 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000012933 diacyl peroxide Substances 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000003599 food sweetener Nutrition 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 150000004668 long chain fatty acids Chemical class 0.000 description 2
- 239000012764 mineral filler Substances 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- -1 saturated aliphatic ketones Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003765 sweetening agent Substances 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 230000009967 tasteless effect Effects 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- XINQFOMFQFGGCQ-UHFFFAOYSA-L (2-dodecoxy-2-oxoethyl)-[6-[(2-dodecoxy-2-oxoethyl)-dimethylazaniumyl]hexyl]-dimethylazanium;dichloride Chemical compound [Cl-].[Cl-].CCCCCCCCCCCCOC(=O)C[N+](C)(C)CCCCCC[N+](C)(C)CC(=O)OCCCCCCCCCCCC XINQFOMFQFGGCQ-UHFFFAOYSA-L 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 1
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
- NFPBWZOKGZKYRE-UHFFFAOYSA-N 2-propan-2-ylperoxypropane Chemical compound CC(C)OOC(C)C NFPBWZOKGZKYRE-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 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
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 240000001238 Gaultheria procumbens Species 0.000 description 1
- 235000007297 Gaultheria procumbens Nutrition 0.000 description 1
- 244000303040 Glycyrrhiza glabra Species 0.000 description 1
- 235000006200 Glycyrrhiza glabra Nutrition 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 244000024873 Mentha crispa Species 0.000 description 1
- 235000014749 Mentha crispa Nutrition 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- 240000001987 Pyrus communis Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 244000290333 Vanilla fragrans Species 0.000 description 1
- 235000009499 Vanilla fragrans Nutrition 0.000 description 1
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 description 1
- XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- UJRIYYLGNDXVTA-UHFFFAOYSA-N ethenyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC=C UJRIYYLGNDXVTA-UHFFFAOYSA-N 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- KAEAMHPPLLJBKF-UHFFFAOYSA-N iron(3+) sulfide Chemical compound [S-2].[S-2].[S-2].[Fe+3].[Fe+3] KAEAMHPPLLJBKF-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000011477 liquorice Nutrition 0.000 description 1
- 230000018984 mastication Effects 0.000 description 1
- 238000010077 mastication Methods 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- YCJYNBLLJHFIIW-MBABXGOBSA-N validoxylamine A Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)C[C@@H]1N[C@@H]1[C@H](O)[C@@H](O)[C@H](O)C(CO)=C1 YCJYNBLLJHFIIW-MBABXGOBSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
- A23G4/08—Chewing gum characterised by the composition containing organic or inorganic compounds of the chewing gum base
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L31/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
- C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
- C08L31/04—Homopolymers or copolymers of vinyl acetate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
Landscapes
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Confectionery (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51608865A | 1965-12-23 | 1965-12-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1617908A1 true DE1617908A1 (de) | 1972-01-05 |
Family
ID=24054087
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19661617908 Pending DE1617908A1 (de) | 1965-12-23 | 1966-12-16 | Grundlage fuer Kaugummi |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3440060A (enExample) |
| BE (1) | BE691529A (enExample) |
| DE (1) | DE1617908A1 (enExample) |
| FR (1) | FR1505267A (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4069307A (en) | 1970-10-01 | 1978-01-17 | Alza Corporation | Drug-delivery device comprising certain polymeric materials for controlled release of drug |
| US4144317A (en) | 1975-05-30 | 1979-03-13 | Alza Corporation | Device consisting of copolymer having acetoxy groups for delivering drugs |
| JPS5455761A (en) * | 1977-10-12 | 1979-05-04 | Takasago Perfumery Co Ltd | Chewing gum base containing heat decomposed product of natural robber and production thereof |
| US4525363A (en) * | 1983-06-29 | 1985-06-25 | Nabisco Brands, Inc. | Single compatibilizing agents for elastomer-resin combination gum base |
| US4582628A (en) * | 1983-08-29 | 1986-04-15 | Petrolite Corporation | Vinyl-type interpolymers and uses thereof |
| US4968511A (en) * | 1989-03-10 | 1990-11-06 | Amelia Ronald P D | Composition and process for one-step chewing gum |
| US5116627A (en) * | 1991-03-07 | 1992-05-26 | International Flavors & Fragrances Inc. | Chewing gum containing compositions for controlled release of flavor bearing substances and process for producing same |
| US5173317A (en) * | 1991-10-29 | 1992-12-22 | Wm. Wrigley Jr. Company | Gum compositions containing vinyl laurate/vinyl acetate copolymer |
| US5424080A (en) * | 1992-06-30 | 1995-06-13 | Wm. Wrigley Jr. Company | Wax-free chewing gum base |
| AU2002249101B2 (en) * | 2001-03-23 | 2005-10-20 | Gumlink A/S | Coated degradable chewing gum with improved shelf life and process for preparing same |
| US20040156949A1 (en) * | 2001-03-23 | 2004-08-12 | Lone Andersen | Degradable elastomers for chewing gum base |
| US20040180111A1 (en) * | 2001-03-23 | 2004-09-16 | Lone Andersen | Degradable resin substitute for chewing gum |
| ES2554389T3 (es) * | 2001-03-23 | 2015-12-18 | Gumlink A/S | Goma de mascar biodegradable y método para manufacturar tal goma de mascar |
| CN100506060C (zh) * | 2001-03-23 | 2009-07-01 | 古木林科有限公司 | 口香糖的一步制造方法 |
| GB0216413D0 (en) * | 2002-07-15 | 2002-08-21 | Nestle Sa | Tabletted chewing gum sweet |
| ES2311631T3 (es) * | 2002-09-24 | 2009-02-16 | Gumlink A/S | Goma de mascar biodegradable que comprende por lo menos un polimero biodegradable de alto peso molecular. |
| MXPA05002959A (es) * | 2002-09-24 | 2005-06-03 | Gumlink As | Polimero degradable para goma de mascar. |
| RU2303365C2 (ru) * | 2002-09-24 | 2007-07-27 | Гумлинк А/С | Жевательная резинка с улучшенным высвобождением ингредиентов жевательной резинки |
| CN100471398C (zh) | 2002-09-24 | 2009-03-25 | 古木林科有限公司 | 包括至少两种不同的生物可降解聚合物的口香糖 |
| DE60234884D1 (de) * | 2002-09-24 | 2010-02-04 | Gumlink As | Kaugummi mit niedrigem Feuchtigkeitsgehalt |
| RU2342846C2 (ru) * | 2003-02-04 | 2009-01-10 | Гумлинк А/С | Таблетка прессованной жевательной резинки и способ ее производства |
| DE60323055D1 (de) * | 2003-05-06 | 2008-10-02 | Gumlinck As | Methode zur Herstellung von Kaugummigranulat und komprimierten Kaugummiprodukten, sowie ein Kaugummigranuliersystem |
| EP1474995B1 (en) * | 2003-05-06 | 2012-11-14 | Gumlink A/S | A method for producing chewing gum granules, a gum composition extruder and granulating system, and a chewing gum product |
| JP2007525146A (ja) * | 2003-12-30 | 2007-09-06 | ガムリンク エー／エス | 生分解性ポリマーを含み且つ分解性を促進させたチューインガム |
| ES2351969T3 (es) * | 2003-12-30 | 2011-02-14 | Gumlink A/S | Chicle biodegradable comprimido. |
| DK200401195A (da) * | 2004-08-06 | 2004-08-06 | Gumlink As | Layered chewing gum tablet |
| AU2004323874A1 (en) * | 2004-10-08 | 2006-04-13 | Gumlink A/S | Confectionery product |
| WO2006066572A2 (en) * | 2004-12-22 | 2006-06-29 | Gumlink A/S | Biodegradable chewing gum comprising biodegradable polymer with high glass transition temperature |
| DK1828279T3 (da) * | 2004-12-22 | 2009-06-02 | Gumlink As | Nedbrydelig polymer til tyggegummi |
| EP2028951B1 (en) * | 2006-06-16 | 2011-04-27 | Gumlink A/S | Chewing gum comprising a hydrophobic enzyme formulation |
| IT1397505B1 (it) | 2009-06-25 | 2013-01-16 | Vinavil S P A | Terpolimeri a base di polivinil alcol per formulati di chewing gum a basso impatto adesivo |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2596852A (en) * | 1950-07-14 | 1952-05-13 | Heggie Robert | Permanently flavored chewing gum base |
| US2662016A (en) * | 1950-10-21 | 1953-12-08 | Beech Nut Packing Co | Chewing gum base |
| US3018274A (en) * | 1957-03-05 | 1962-01-23 | Air Reduction | Vinyl acetate copolymers |
| NL126208C (enExample) * | 1961-10-27 |
-
1965
- 1965-12-23 US US516088A patent/US3440060A/en not_active Expired - Lifetime
-
1966
- 1966-12-16 DE DE19661617908 patent/DE1617908A1/de active Pending
- 1966-12-20 BE BE691529D patent/BE691529A/xx unknown
- 1966-12-21 FR FR88281A patent/FR1505267A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US3440060A (en) | 1969-04-22 |
| FR1505267A (fr) | 1967-12-08 |
| BE691529A (enExample) | 1967-06-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1617908A1 (de) | Grundlage fuer Kaugummi | |
| DE2406844C3 (de) | Verfahren zum Vernetzen von Polyäthylen und Äthylencopolymerisaten | |
| EP0515855B1 (de) | Hochfliessfähige Propylen-Ethylen-Copolymerisate | |
| DE2728862C3 (de) | Stabilisierte Formmassen auf der Basis von Vinylchlorid-Polymerisaten | |
| DE2238555B2 (de) | Polymermassen aus Copolymeren aus Äthylen, Kohlenmonoxid und einem Termonomeren | |
| DE974268C (de) | Verfahren zur Blockpolymerisation von Styrol | |
| DE2353783C3 (de) | Verfahren zur Herstellung eines vernetzten Copolymeren des Äthylens | |
| DE1745565A1 (de) | Verfahren zur Herstellung von Copolymeren aus AEthylen und Vinylestern | |
| DE1570220C3 (de) | Festes Vinylchiorid-Propylen-Mischpolymerisat, Verfahren zu seiner Herstellung und Verwendung für thermoplastische Formmassen | |
| EP0503361A1 (de) | Teilvernetzte Kunststoffmasse | |
| DE2652458B2 (de) | Hitzestabilisierte Formmassen auf der Basis von Vinylchlorid Homo- oder Copolymerisaten | |
| CH523928A (de) | Warmverformbare Mischung | |
| DE2046898B2 (de) | Verfahren zur herstellung von propfmischpolymerisaten und deren verwendung in polyvinylchlorid enthaltenden formkoerpern | |
| DE2119701A1 (de) | Polymerisatzusammensetzungen | |
| DE1595416A1 (de) | Verfahren zur Herstellung von Vinylchlorid-Polymeren | |
| DE2234038A1 (de) | Verfahren zur polymerisation von vinylchlorid | |
| DE2830324C2 (de) | Polymeres Bindemittel für Kaugummi und dessen Verwendung | |
| DE1720950B2 (de) | Verfahren zur herstellung von vinylchloridharzmassen | |
| DE2435906B2 (de) | Polymere Formmasse | |
| DE1669395A1 (de) | Verwendung von Polypropylen zur Herstellung von Folien,Faeden u.dgl. | |
| DE3782573T2 (de) | Fluessige copolyester-weichmacher aus 1,4-butandiol und einer mischung von dicarbonsaeuren. | |
| DE2203276A1 (de) | Verfahren zur Herstellung von Lacton-Pfropfmischpolymerisaten | |
| DE2323191B2 (de) | Verfahren zur Herstellung eines Polymeren aus Vinylhalogenid nach einem Zwei-Stufen-Massenpolymerisationsverfahren | |
| DE1154620B (de) | Verfahren zum Vernetzen von Polyaethylenmassen | |
| DE1965443C3 (de) | Herstellungsverfahren für modifiziertes Polyvinylchlorid hoher Schlagfestigkeit |