SK279993B6 - Polymérny materiál - Google Patents
Polymérny materiál Download PDFInfo
- Publication number
- SK279993B6 SK279993B6 SK3901-92A SK390192A SK279993B6 SK 279993 B6 SK279993 B6 SK 279993B6 SK 390192 A SK390192 A SK 390192A SK 279993 B6 SK279993 B6 SK 279993B6
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- SK
- Slovakia
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- component
- material according
- polymeric material
- starch
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 41
- 239000000463 material Substances 0.000 claims abstract description 75
- 229920002472 Starch Polymers 0.000 claims abstract description 72
- 235000019698 starch Nutrition 0.000 claims abstract description 72
- 239000008107 starch Substances 0.000 claims abstract description 70
- 239000004014 plasticizer Substances 0.000 claims abstract description 17
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 11
- 239000000654 additive Substances 0.000 claims abstract description 3
- 239000000155 melt Substances 0.000 claims abstract description 3
- 229920000642 polymer Polymers 0.000 claims description 56
- -1 aliphatic hydroxy acids Chemical class 0.000 claims description 54
- 229920001577 copolymer Polymers 0.000 claims description 43
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 31
- 239000005977 Ethylene Substances 0.000 claims description 30
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims description 23
- 229920001610 polycaprolactone Polymers 0.000 claims description 18
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 16
- 229920005862 polyol Polymers 0.000 claims description 16
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 15
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 15
- 125000001931 aliphatic group Chemical group 0.000 claims description 15
- 239000000047 product Substances 0.000 claims description 15
- 239000000600 sorbitol Substances 0.000 claims description 15
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 14
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 14
- 239000012948 isocyanate Substances 0.000 claims description 14
- 150000003077 polyols Chemical class 0.000 claims description 14
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 14
- 150000002596 lactones Chemical class 0.000 claims description 13
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- 238000004519 manufacturing process Methods 0.000 claims description 12
- 239000000178 monomer Substances 0.000 claims description 12
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- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 9
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- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- 230000007062 hydrolysis Effects 0.000 claims description 8
- 238000006460 hydrolysis reaction Methods 0.000 claims description 8
- 150000002513 isocyanates Chemical class 0.000 claims description 8
- 150000001241 acetals Chemical class 0.000 claims description 7
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- 238000006243 chemical reaction Methods 0.000 claims description 7
- 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 claims description 6
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 6
- 239000008103 glucose Substances 0.000 claims description 6
- 229920001519 homopolymer Polymers 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 5
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 5
- 229930195725 Mannitol Natural products 0.000 claims description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 5
- 230000001588 bifunctional effect Effects 0.000 claims description 5
- 239000004202 carbamide Substances 0.000 claims description 5
- 239000000594 mannitol Substances 0.000 claims description 5
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- 150000002895 organic esters Chemical class 0.000 claims description 5
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 5
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 5
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 5
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 5
- 239000004416 thermosoftening plastic Substances 0.000 claims description 5
- UNVGBIALRHLALK-UHFFFAOYSA-N 1,5-Hexanediol Chemical compound CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 4
- 239000004970 Chain extender Substances 0.000 claims description 4
- 150000001299 aldehydes Chemical group 0.000 claims description 4
- 150000001414 amino alcohols Chemical class 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 239000001913 cellulose Substances 0.000 claims description 4
- 229920002678 cellulose Polymers 0.000 claims description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 4
- 125000005442 diisocyanate group Chemical group 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 4
- 150000004676 glycans Chemical class 0.000 claims description 4
- 150000002485 inorganic esters Chemical class 0.000 claims description 4
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- 229920000223 polyglycerol Polymers 0.000 claims description 4
- 229920001451 polypropylene glycol Polymers 0.000 claims description 4
- 229920001282 polysaccharide Polymers 0.000 claims description 4
- 239000005017 polysaccharide Substances 0.000 claims description 4
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 3
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 3
- 229920000856 Amylose Polymers 0.000 claims description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 3
- 229920003232 aliphatic polyester Polymers 0.000 claims description 3
- 150000008064 anhydrides Chemical class 0.000 claims description 3
- 159000000032 aromatic acids Chemical class 0.000 claims description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 3
- 229920002301 cellulose acetate Polymers 0.000 claims description 3
- 150000005690 diesters Chemical class 0.000 claims description 3
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 claims description 3
- 150000002009 diols Chemical class 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 2
- KULQACNMKIDJNN-GASJEMHNSA-N (2r,3s,4r,5r)-1-aminohexane-1,2,3,4,5,6-hexol Chemical compound NC(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO KULQACNMKIDJNN-GASJEMHNSA-N 0.000 claims description 2
- IWHLYPDWHHPVAA-UHFFFAOYSA-N 6-hydroxyhexanoic acid Chemical compound OCCCCCC(O)=O IWHLYPDWHHPVAA-UHFFFAOYSA-N 0.000 claims description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 2
- 229920000881 Modified starch Polymers 0.000 claims description 2
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 claims description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 2
- 150000001279 adipic acids Chemical class 0.000 claims description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 150000001413 amino acids Chemical class 0.000 claims description 2
- 229920006187 aquazol Polymers 0.000 claims description 2
- 229910021538 borax Inorganic materials 0.000 claims description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004327 boric acid Substances 0.000 claims description 2
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 claims description 2
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 claims description 2
- 150000002311 glutaric acids Chemical class 0.000 claims description 2
- 150000002334 glycols Chemical class 0.000 claims description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 2
- GFMIDCCZJUXASS-UHFFFAOYSA-N hexane-1,1,6-triol Chemical compound OCCCCCC(O)O GFMIDCCZJUXASS-UHFFFAOYSA-N 0.000 claims description 2
- WJSATVJYSKVUGV-UHFFFAOYSA-N hexane-1,3,5-triol Chemical compound CC(O)CC(O)CCO WJSATVJYSKVUGV-UHFFFAOYSA-N 0.000 claims description 2
- 229920001600 hydrophobic polymer Polymers 0.000 claims description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 2
- 235000019426 modified starch Nutrition 0.000 claims description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- VGTPKLINSHNZRD-UHFFFAOYSA-N oxoborinic acid Chemical compound OB=O VGTPKLINSHNZRD-UHFFFAOYSA-N 0.000 claims description 2
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- ZBTJXGYIGWGHSV-LTYVRWIXSA-N (4s,5r,6r,7r)-3,4,5,6,7,8-hexahydroxyoctanoic acid;sodium Chemical compound [Na].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)CC(O)=O ZBTJXGYIGWGHSV-LTYVRWIXSA-N 0.000 claims 1
- TURGQPDWYFJEDY-UHFFFAOYSA-N 1-hydroperoxypropane Chemical compound CCCOO TURGQPDWYFJEDY-UHFFFAOYSA-N 0.000 claims 1
- BUKOWKOPJSGGQK-UHFFFAOYSA-N 6-hydroxy caprylic acid Chemical compound CCC(O)CCCCC(O)=O BUKOWKOPJSGGQK-UHFFFAOYSA-N 0.000 claims 1
- IQBGVZDRJBTLDN-UHFFFAOYSA-N 6-hydroxy-3,7-dimethyloctanoic acid Chemical compound CC(C)C(O)CCC(C)CC(O)=O IQBGVZDRJBTLDN-UHFFFAOYSA-N 0.000 claims 1
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- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- RZXDTJIXPSCHCI-UHFFFAOYSA-N hexa-1,5-diene-2,5-diol Chemical class OC(=C)CCC(O)=C RZXDTJIXPSCHCI-UHFFFAOYSA-N 0.000 claims 1
- HOVAGTYPODGVJG-ZFYZTMLRSA-N methyl alpha-D-glucopyranoside Chemical compound CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HOVAGTYPODGVJG-ZFYZTMLRSA-N 0.000 claims 1
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- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical group OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 2
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L87/00—Compositions of unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/06—Biodegradable
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L29/00—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 alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
- C08L29/02—Homopolymers or copolymers of unsaturated alcohols
- C08L29/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/06—Polyurethanes from polyesters
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Water Supply & Treatment (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hematology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Biological Depolymerization Polymers (AREA)
- Materials For Medical Uses (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Dental Preparations (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITTO910327A IT1245485B (it) | 1991-05-03 | 1991-05-03 | Membrane permselettive e loro impiego |
| EP91112942A EP0525245A1 (de) | 1991-08-01 | 1991-08-01 | Absorbierender Einwegartikel |
| ITTO920199A IT1256693B (it) | 1992-03-10 | 1992-03-10 | Composizione polimerica amidacea filmabile, ed articoli sagomati, particolarmente film e foglie ottenibili da tale composizione, aventi elevato effetto barriera e procedimento relativo. |
| ITTO920282A IT1263114B (it) | 1992-03-27 | 1992-03-27 | Composizione polimerica amidacea biodegradabile |
| PCT/EP1992/000959 WO1992019680A1 (en) | 1991-05-03 | 1992-05-04 | Biodegradable polymeric compositions based on starch and thermoplastic polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK390192A3 SK390192A3 (en) | 1994-12-07 |
| SK279993B6 true SK279993B6 (sk) | 1999-06-11 |
Family
ID=27442155
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK3901-92A SK279993B6 (sk) | 1991-05-03 | 1992-05-04 | Polymérny materiál |
Country Status (20)
| Country | Link |
|---|---|
| EP (1) | EP0539541B1 (de) |
| JP (1) | JP2527523B2 (de) |
| KR (1) | KR960008112B1 (de) |
| AT (1) | ATE155161T1 (de) |
| AU (1) | AU658180B2 (de) |
| BR (1) | BR9205258A (de) |
| CA (1) | CA2084994C (de) |
| CZ (1) | CZ285748B6 (de) |
| DE (2) | DE69220754T2 (de) |
| DK (1) | DK0539541T3 (de) |
| ES (1) | ES2103943T3 (de) |
| FI (1) | FI115138B (de) |
| GR (1) | GR3024078T3 (de) |
| HU (1) | HU216971B (de) |
| LV (1) | LV12151B (de) |
| NO (1) | NO319011B1 (de) |
| PL (1) | PL174799B1 (de) |
| RU (1) | RU2095379C1 (de) |
| SK (1) | SK279993B6 (de) |
| WO (1) | WO1992019680A1 (de) |
Families Citing this family (99)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE147995T1 (de) * | 1991-06-26 | 1997-02-15 | Procter & Gamble | Saugfähige einwegartikel mit biodegradierbare schutzfolien |
| PL173320B1 (pl) * | 1991-06-26 | 1998-02-27 | Procter & Gamble | Folia ulegajaca rozkładowi biologicznemu i nieprzenikalna dla płynów |
| ES2112327T3 (es) * | 1991-08-07 | 1998-04-01 | Clopay Corp | Una pelicula termoplastica biodegradable y metodo para producirla. |
| US5939467A (en) * | 1992-06-26 | 1999-08-17 | The Procter & Gamble Company | Biodegradable polymeric compositions and products thereof |
| ATE163883T1 (de) * | 1992-06-26 | 1998-03-15 | Procter & Gamble | Biologisch abbaubare, flüssigkeitsundurchlässige mehrschichtfolienzusammensetzung |
| FR2693734B1 (fr) * | 1992-07-15 | 1994-10-07 | Roquette Freres | Composition thermoformable-biodécomposable à base d'un composé amylacé et d'un polyester biodégradable. |
| US5703160A (en) * | 1992-07-15 | 1997-12-30 | Solvay S.A. | Biodegradable moulding compositions comprising a starch, a biodegradable polyester, and a salt of a hydroxycarboxylic acid |
| US5312850A (en) * | 1993-01-04 | 1994-05-17 | National Starch And Chemical Investment Holding Corporation | Polylactide and starch containing hot melt adhesive |
| AU659353B2 (en) * | 1992-10-29 | 1995-05-11 | National Starch And Chemical Investment Holding Corporation | Polylactide containing hot melt adhesive |
| US5252646A (en) * | 1992-10-29 | 1993-10-12 | National Starch And Chemical Investment Holding Corporation | Polylactide containing hot melt adhesive |
| US5844023A (en) | 1992-11-06 | 1998-12-01 | Bio-Tec Biologische Naturverpackungen Gmbh | Biologically degradable polymer mixture |
| DE4237535C2 (de) † | 1992-11-06 | 2000-05-25 | Biotec Biolog Naturverpack | Biologisch abbaubare Polymermischung, ein Verfahren und eine Folie |
| US5393804A (en) * | 1992-11-24 | 1995-02-28 | Parke, Davis & Company | Biodegradable compositions comprising starch and alkenol polymers |
| BR9405651A (pt) * | 1993-01-08 | 1995-11-14 | Novon International Inc | Composição de mistura de polímeros termoplásticos biodegradáveis; processo de preparar a mesma; artigo formado; filme e fibra |
| US5910520A (en) * | 1993-01-15 | 1999-06-08 | Mcneil-Ppc, Inc. | Melt processable biodegradable compositions and articles made therefrom |
| DE4317696C1 (de) * | 1993-05-27 | 1994-12-22 | Biotec Biolog Naturverpack | Verfahren zur Herstellung von gekörnter, thermoplastischer Stärke |
| GB9311399D0 (en) * | 1993-06-02 | 1993-07-21 | Zeneca Ltd | Polyester composition |
| EP0723572B1 (de) * | 1993-10-15 | 1999-12-08 | H.B. Fuller Licensing & Financing, Inc. | Biologisch abbaubare bzw. kompostierbare hot melt-klebstoffe, enthaltend polyester auf basis von milchsäure |
| US5500465A (en) * | 1994-03-10 | 1996-03-19 | Board Of Trustees Operating Michigan State University | Biodegradable multi-component polymeric materials based on unmodified starch-like polysaccharides |
| FI98818C (fi) * | 1994-03-21 | 1997-08-25 | Valtion Teknillinen | Alifaattisilla polyestereillä oksastetut tärkkelysjohdannaiset ja menetelmä niiden valmistamiseksi sekä käyttö |
| US5739244A (en) * | 1994-03-23 | 1998-04-14 | Fisk; Donald | Polymer composition containing prime starch |
| IT1271316B (it) | 1994-12-23 | 1997-05-27 | Novamont Spa | Bastoncini cotonati in materiale plastico |
| CN1083020C (zh) * | 1995-02-14 | 2002-04-17 | 智索股份有限公司 | 可生物降解的纤维和非织造布 |
| US5540929A (en) * | 1995-03-08 | 1996-07-30 | Board Of Trustees Operating Michigan State University | Polysaccharides grafted with aliphatic polyesters derived from cyclic esters |
| ES2201173T3 (es) * | 1995-04-07 | 2004-03-16 | BIO-TEC BIOLOGISCHE NATURVERPACKUNGEN GMBH & CO. KG | Mezcla de polimeros biologicamente degradable. |
| FR2735483B1 (fr) * | 1995-06-13 | 1997-08-08 | Potency Sarl | Materiau composite totalement biodegradable et procede de fabrication de ce materiau |
| CA2226579A1 (en) * | 1995-07-12 | 1997-01-30 | Valtion Teknillinen Tutkimuskeskus | Thermoplasticized starch component and process for the preparation thereof |
| DE19624641A1 (de) | 1996-06-20 | 1998-01-08 | Biotec Biolog Naturverpack | Biologisch abbaubarer Werkstoff, bestehend im wesentlichen aus oder auf Basis thermoplastischer Stärke |
| DE19630232A1 (de) * | 1996-07-26 | 1998-01-29 | Wolff Walsrode Ag | Monoaxial gereckte, biologisch abbbaubare und kompostierbare Folie mit verbesserten Eigenschaften |
| EP0950690B1 (de) | 1996-11-05 | 2005-01-26 | NOVAMONT S.p.A. | Biologisch abbaubare Polymerzusammensetzungen, die Stärke und ein thermoplastisches Polymer enthalten |
| DE19729306C2 (de) | 1997-07-09 | 2002-04-04 | Celanese Ventures Gmbh | Stärke und/oder modifizierte Stärke und Weichmacher enthaltende Zusammensetzungen sowie Verfahren und Verwendung |
| DE19750846C1 (de) | 1997-11-17 | 2000-01-27 | Biop Biopolymer Gmbh | Verfahren zur Herstellung einer Komponente für die Herstellung von Polymermischungen auf der Basis von Stärke |
| DE19805925A1 (de) * | 1998-02-13 | 1999-08-19 | Kalle Nalo Gmbh | Wursthülle mit Stärke oder Stärkederivaten sowie Verfahren zu ihrer Herstellung |
| CA2324949A1 (en) * | 1998-03-24 | 1999-09-30 | Avantgarb, Llc | Modified textile and other materials and methods for their preparation |
| US6380336B1 (en) | 1998-03-24 | 2002-04-30 | Nano-Tex, Llc | Copolymers and oil-and water-repellent compositions containing them |
| DE19824968A1 (de) * | 1998-06-04 | 1999-12-09 | Kalle Nalo Gmbh & Co Kg | Von einem Netz umgebene, schlauchförmige Hülle für ein pastöses Füllgut sowie Verfahren zu ihrer Herstellung |
| ITTO980524A1 (it) | 1998-06-17 | 1999-12-17 | Novamont Spa | Composizioni contenenti amido aventi elevata resistenza all'invecchiam ento. |
| ES2216425T3 (es) * | 1998-12-16 | 2004-10-16 | Kuraray Co., Ltd. | Fibras termoplasticas de alcohol polivinilico y su procedimiento de preparacion. |
| WO2000039212A1 (de) * | 1998-12-23 | 2000-07-06 | Bio-Tec Biologische Naturverpackungen Gmbh & Co. Kg | Biologisch abbaubare polymerwerkstoffe bzw. ternäre polymermischungen auf basis polysaccharid oder polysaccharid-derivat |
| ES2243160T3 (es) * | 1999-03-08 | 2005-12-01 | THE PROCTER & GAMBLE COMPANY | Estructura absorbente, flexible, que comprende fibras de almidon. |
| IT1315241B1 (it) | 1999-10-12 | 2003-02-03 | Isagro Spa | Dispositivo biodegradabile ad azione attraente per la lotta agliinsetti. |
| CA2414197C (en) * | 2000-07-24 | 2010-08-24 | Dow Global Technologies Inc. | Thermoplastic superabsorbent polymer blend compositions and their preparation |
| KR100396937B1 (ko) * | 2000-07-29 | 2003-09-02 | 정효식 | 생분해성 및 가수분해성을 갖는 수지 조성물 |
| US6573340B1 (en) | 2000-08-23 | 2003-06-03 | Biotec Biologische Naturverpackungen Gmbh & Co. Kg | Biodegradable polymer films and sheets suitable for use as laminate coatings as well as wraps and other packaging materials |
| KR100402549B1 (ko) * | 2000-12-20 | 2003-10-22 | 휴마트로 코포래이션 | 가요성 구조물을 위한 전분 필라멘트의 전기방사 제조공정 |
| ITTO20010058A1 (it) | 2001-01-25 | 2002-07-25 | Novamont Spa | Miscele ternarie di poliesteri biodegradabili e prodotti da queste ottenuti. |
| ITTO20010060A1 (it) | 2001-01-25 | 2002-07-25 | Novamont Spa | Miscele ternartie di poliesteri alifatici biodegradabili e prodotti da queste ottenuti. |
| US7297394B2 (en) | 2002-03-01 | 2007-11-20 | Bio-Tec Biologische Naturverpackungen Gmbh & Co. Kg | Biodegradable films and sheets suitable for use as coatings, wraps and packaging materials |
| US7241832B2 (en) | 2002-03-01 | 2007-07-10 | bio-tec Biologische Naturverpackungen GmbH & Co., KG | Biodegradable polymer blends for use in making films, sheets and other articles of manufacture |
| US7077994B2 (en) † | 2001-10-19 | 2006-07-18 | The Procter & Gamble Company | Polyhydroxyalkanoate copolymer/starch compositions for laminates and films |
| DE10208858A1 (de) | 2002-03-01 | 2003-09-11 | Kalle Gmbh & Co Kg | Rauch- und wasserdampfdurchlässige Nahrungsmittelhülle aus einem thermoplastischen Gemisch |
| CN1230466C (zh) * | 2003-02-25 | 2005-12-07 | 丁少忠 | 一种可完全生物降解塑料母料及其制备方法 |
| US7172814B2 (en) | 2003-06-03 | 2007-02-06 | Bio-Tec Biologische Naturverpackungen Gmbh & Co | Fibrous sheets coated or impregnated with biodegradable polymers or polymers blends |
| US7714065B2 (en) * | 2003-12-17 | 2010-05-11 | The Procter & Gamble Company | Polymeric structures comprising a hydrophile/lipophile system |
| CN101061167B (zh) * | 2004-10-05 | 2010-12-15 | 普朗蒂克科技有限公司 | 可成型的生物降解性聚合物 |
| CN100506927C (zh) | 2005-03-21 | 2009-07-01 | 刘景春 | 多质离散效应纳米结构液膜及其制备方法和应用 |
| CN104945683A (zh) * | 2006-04-18 | 2015-09-30 | 普朗蒂克科技有限公司 | 聚合物膜 |
| US8414939B2 (en) | 2006-07-31 | 2013-04-09 | Wm. Wrigley Jr. Company | Food product with an encapsulated lecithin material |
| ITMI20061845A1 (it) | 2006-09-27 | 2008-03-28 | Novamont Spa | Composizioni biodegradabili polifasiche a base di amido |
| EP2115008B1 (de) | 2007-03-01 | 2019-09-18 | De Staat der Nederlanden, vert. door de Minister van Volksgezondheid, Welzijn en Sport, namens de Minister, Projectdirectie ALT, het INTRAVACC | Auf offener stärke basierendes, biologisch abbaubares material |
| KR100888088B1 (ko) | 2007-11-14 | 2009-03-11 | (주)에코메이트코리아 | 내열성이 개선된 생분해성 수지 조성물 |
| CN102099419B (zh) * | 2008-06-18 | 2013-10-23 | 巴斯夫欧洲公司 | 乙二醛和甲基乙二醛作为聚合物共混物的添加剂 |
| US20110313075A1 (en) | 2008-09-29 | 2011-12-22 | Basf Se | Aliphatic polyester |
| JP5518077B2 (ja) | 2008-09-29 | 2014-06-11 | ビーエーエスエフ ソシエタス・ヨーロピア | 紙をコートする方法 |
| CN102165013B (zh) | 2008-09-29 | 2013-04-24 | 巴斯夫欧洲公司 | 可生物降解的聚合物混合物 |
| RU2485144C2 (ru) * | 2008-11-05 | 2013-06-20 | Тейдзин Кемикалз Лтд. | Композиция полимера молочной кислоты и формованное изделие из данной композиции |
| WO2010069804A1 (de) | 2008-12-19 | 2010-06-24 | Basf Se | Verfahren zur herstellung eines verbundbauteils durch mehrkomponentenspritzguss |
| WO2010100052A1 (de) | 2009-03-03 | 2010-09-10 | Basf Se | Verbackungsresistentes polyalkylencarbonat |
| FR2947557B1 (fr) | 2009-07-03 | 2011-12-09 | Ulice | Procede de production de materiau biodegradable |
| CN101608058B (zh) * | 2009-07-16 | 2010-08-25 | 任伟 | 一种全降解仿纸材料及其制备方法 |
| WO2011020170A1 (en) * | 2009-08-18 | 2011-02-24 | National Research Council Of Canada | Process of producing thermoplastic starch/polymer blends |
| US8658069B2 (en) | 2009-11-09 | 2014-02-25 | Basf Se | Method for producing shrink films |
| WO2011117203A1 (de) | 2010-03-24 | 2011-09-29 | Basf Se | Verfahren zur folienherstellung |
| EP2550330A1 (de) | 2010-03-24 | 2013-01-30 | Basf Se | Verfahren zur herstellung von clingfolien |
| AU2011322685A1 (en) | 2010-10-27 | 2013-05-23 | Basf Se | Use of polymer blends for producing slit film tapes |
| WO2012113744A1 (de) | 2011-02-23 | 2012-08-30 | Basf Se | Polyesterfolie enthaltend nährsalze |
| US8546472B2 (en) | 2011-03-23 | 2013-10-01 | Basf Se | Polyesters based on 2-methylsuccinic acid |
| EP2688956A1 (de) | 2011-03-23 | 2014-01-29 | Basf Se | Polyester auf basis von 2-methylbernsteinsaeure |
| EP2551301A1 (de) | 2011-07-29 | 2013-01-30 | Basf Se | Biologisch abbaubare Polyesterfolie |
| RU2490289C1 (ru) * | 2012-02-02 | 2013-08-20 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Московский государственный университет пищевых производств" Министерства образования и науки Российской Федерации | Биологически разрушаемая высоконаполненная термопластичная композиция с использованием крахмала и наномодификатора |
| PL2831186T3 (pl) * | 2012-03-28 | 2020-01-31 | Thüringisches Institut Für Textil- Und Kunststoff- Forschung E.V. | Wielofunkcyjne warstewki powlekające, które mogą być stosowane w formie ciekłej |
| CN104428369B (zh) | 2012-07-09 | 2016-10-12 | 巴斯夫欧洲公司 | 聚合物混合物的完全厌氧消化的方法 |
| WO2014009176A1 (de) | 2012-07-10 | 2014-01-16 | Basf Se | Verfahren zum vollständigen anaeroben abbau von polymermischungen |
| KR20150086491A (ko) | 2012-11-15 | 2015-07-28 | 바스프 에스이 | 생분해성 폴리에스테르 혼합물 |
| US9056979B2 (en) | 2012-11-15 | 2015-06-16 | Basf Se | Biodegradable polyester mixture |
| EP2826817B1 (de) | 2013-07-15 | 2017-07-05 | Basf Se | Biologisch abbaubare polyestermischung |
| DE102014223786A1 (de) | 2013-12-10 | 2015-06-11 | Basf Se | Polymermischung für Barrierefilm |
| WO2016087372A1 (de) | 2014-12-05 | 2016-06-09 | Basf Se | Biologisch abbaubare copolyester |
| DE102015217309A1 (de) | 2015-09-10 | 2017-03-16 | Basf Se | Polymerzusammensetzung |
| US10077333B2 (en) | 2016-04-20 | 2018-09-18 | Elevance Renewable Sciences, Inc. | Renewably derived polyesters and methods of making and using the same |
| RU2629680C1 (ru) * | 2016-06-21 | 2017-08-31 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Национальный исследовательский Мордовский государственный университет им. Н.П. Огарёва" | Полимерная композиция для изготовления биодеградируемых изделий |
| US11072683B2 (en) | 2016-12-22 | 2021-07-27 | Basf Se | Furandicarboxylic acid-containing polyesters |
| ES2895041T3 (es) | 2017-06-19 | 2022-02-17 | Basf Se | Película de tres capas biodegradable |
| JP2019006900A (ja) * | 2017-06-26 | 2019-01-17 | プランティック・テクノロジーズ・リミテッド | 樹脂組成物およびその製造方法 |
| PT3891208T (pt) | 2018-12-06 | 2023-05-02 | Basf Se | Processo para produzir um (co) poliéster |
| GB201913593D0 (en) * | 2019-09-20 | 2019-11-06 | Norner Verdandi As | Composition |
| RU2746725C1 (ru) * | 2019-12-26 | 2021-04-19 | Федеральное государственное автономное образовательное учреждение высшего образования "Национальный исследовательский университет "Московский институт электронной техники" | Способ получения биодеградируемого покрытия с высокой гидрофильностью на основе биополимера |
| PL433862A1 (pl) | 2020-05-07 | 2021-11-08 | Grupa Azoty Spółka Akcyjna | Sposób wytwarzania skrobi termoplastycznej i skrobia termoplastyczna |
| WO2024074561A1 (en) | 2022-10-05 | 2024-04-11 | Basf Se | Biodegradable polymer blend and use thereof |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ221198A (en) * | 1986-08-05 | 1990-09-26 | Chisso Corp | Granular fertiliser with poly-3-hydrox-3-alkylpropionic acid coating |
| GB2214918B (en) * | 1988-02-03 | 1992-10-07 | Warner Lambert Co | Polymeric materials made from starch and at least one synthetic thermoplastic polymeric material |
| JP2679837B2 (ja) * | 1989-02-23 | 1997-11-19 | 中興化成工業株式会社 | 生分解性複合材料 |
| IT1233599B (it) * | 1989-05-30 | 1992-04-06 | Butterfly Srl | Composizioni polimeriche per la produzione di articoli di materiale plastico biodegradabile e procedimenti per la loro preparazione |
| CN1048864A (zh) * | 1989-07-18 | 1991-01-30 | 沃纳-兰伯特公司 | 含有无序结构淀粉的以聚合物为基料的混合组合物 |
| EP0444880B1 (de) * | 1990-02-28 | 1997-05-07 | Director-General Of The Agency Of Industrial Science And Technology | Verfahren zur Herstellung eines bioabbaubaren, formbaren Materials |
| JPH03263441A (ja) * | 1990-03-12 | 1991-11-22 | Kuraray Co Ltd | 生分解性組成物、フイルムおよび農業用マルチフイルム |
| JP3068174B2 (ja) * | 1990-10-30 | 2000-07-24 | 株式会社島津製作所 | 生分解性プラスチック |
| JPH04248851A (ja) * | 1991-01-25 | 1992-09-04 | Jsp Corp | 微生物分解性組成物及びシート |
| IT1245408B (it) * | 1991-02-20 | 1994-09-20 | Butterfly Srl | Composizioni polimeriche biodegradabili a base di amido e di polimero termoplastico |
-
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- 1992-05-04 DE DE69220754T patent/DE69220754T2/de not_active Expired - Lifetime
- 1992-05-04 AT AT92909158T patent/ATE155161T1/de not_active IP Right Cessation
- 1992-05-04 ES ES92909158T patent/ES2103943T3/es not_active Expired - Lifetime
- 1992-05-04 HU HU9204174A patent/HU216971B/hu not_active IP Right Cessation
- 1992-05-04 EP EP92909158A patent/EP0539541B1/de not_active Expired - Lifetime
- 1992-05-04 RU RU9292016573A patent/RU2095379C1/ru not_active IP Right Cessation
- 1992-05-04 JP JP4508540A patent/JP2527523B2/ja not_active Expired - Fee Related
- 1992-05-04 CZ CS923901A patent/CZ285748B6/cs not_active IP Right Cessation
- 1992-05-04 KR KR1019920703404A patent/KR960008112B1/ko not_active IP Right Cessation
- 1992-05-04 DK DK92909158.5T patent/DK0539541T3/da active
- 1992-05-04 PL PL92297375A patent/PL174799B1/pl not_active IP Right Cessation
- 1992-05-04 CA CA002084994A patent/CA2084994C/en not_active Expired - Lifetime
- 1992-05-04 SK SK3901-92A patent/SK279993B6/sk unknown
- 1992-05-04 AU AU16509/92A patent/AU658180B2/en not_active Ceased
- 1992-05-04 DE DE0539541T patent/DE539541T1/de active Pending
- 1992-05-04 WO PCT/EP1992/000959 patent/WO1992019680A1/en active IP Right Grant
- 1992-12-30 NO NO19925049A patent/NO319011B1/no not_active IP Right Cessation
- 1992-12-31 FI FI925978A patent/FI115138B/fi not_active IP Right Cessation
-
1997
- 1997-07-10 GR GR970401484T patent/GR3024078T3/el unknown
-
1998
- 1998-02-12 LV LVP-98-22A patent/LV12151B/en unknown
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