JP2527523C - - Google Patents

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Publication number

JP2527523C

JP2527523C JP2527523C JP 2527523 C JP2527523 C JP 2527523C JP 2527523 C JP2527523 C JP 2527523C

Authority

JP

Japan

Prior art keywords

weight

component

composition according

starch

polymer

Prior art date

1999-05-24

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.)

Expired - Lifetime

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• 239000000203 mixture Substances 0.000 claims description 108
• 229920002472 Starch Polymers 0.000 claims description 66
• 235000019698 starch Nutrition 0.000 claims description 66
• 239000008107 starch Substances 0.000 claims description 65
• 229920000642 polymer Polymers 0.000 claims description 63
• -1 aliphatic hydroxyacid Chemical class 0.000 claims description 48
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
• 229920001577 copolymer Polymers 0.000 claims description 19
• 230000000875 corresponding Effects 0.000 claims description 19
• 238000002844 melting Methods 0.000 claims description 18
• 239000004014 plasticizer Substances 0.000 claims description 18
• 125000004432 carbon atoms Chemical group C* 0.000 claims description 17
• PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 17
• 229920001610 polycaprolactone Polymers 0.000 claims description 17
• 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
• 229920005862 polyol Polymers 0.000 claims description 15
• 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 14
• 229920000219 Ethylene vinyl alcohol Polymers 0.000 claims description 14
• 239000000600 sorbitol Substances 0.000 claims description 14
• 239000005977 Ethylene Substances 0.000 claims description 13
• 125000001931 aliphatic group Chemical group 0.000 claims description 13
• 150000002596 lactones Chemical class 0.000 claims description 13
• 229920000728 polyester Polymers 0.000 claims description 13
• 150000003077 polyols Chemical class 0.000 claims description 13
• 229920001059 synthetic polymer Polymers 0.000 claims description 13
• 239000002253 acid Substances 0.000 claims description 12
• 229920002451 polyvinyl alcohol Polymers 0.000 claims description 12
• 229920001169 thermoplastic Polymers 0.000 claims description 12
• XSQUKJJJFZCRTK-UHFFFAOYSA-N urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 12
• VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 11
• 235000011187 glycerol Nutrition 0.000 claims description 11
• 239000004372 Polyvinyl alcohol Substances 0.000 claims description 10
• 125000003118 aryl group Chemical group 0.000 claims description 10
• DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 10
• WMGFVAGNIYUEEP-WUYNJSITSA-N Amylopectin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)O[C@H](OC[C@@H]2[C@H]([C@H](O)[C@@H](O)[C@@H](O[C@@H]3[C@H](O[C@H](O)[C@H](O)[C@H]3O)CO)O2)O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@H]1O WMGFVAGNIYUEEP-WUYNJSITSA-N 0.000 claims description 9
• 229920000945 Amylopectin Polymers 0.000 claims description 9
• FBPFZTCFMRRESA-KAZBKCHUSA-N D-Mannitol Natural products OC[C@@H](O)[C@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KAZBKCHUSA-N 0.000 claims description 9
• 238000006243 chemical reaction Methods 0.000 claims description 9
• LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
• WQZGKKKJIJFFOK-GASJEMHNSA-N D-Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 7
• 229960004063 Propylene glycol Drugs 0.000 claims description 7
• 150000001241 acetals Chemical class 0.000 claims description 7
• QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 7
• JJTUDXZGHPGLLC-UHFFFAOYSA-N dilactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 claims description 7
• 239000008103 glucose Substances 0.000 claims description 7
• 238000006460 hydrolysis reaction Methods 0.000 claims description 7
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
• 239000000047 product Substances 0.000 claims description 7
• 235000013772 propylene glycol Nutrition 0.000 claims description 7
• 239000011780 sodium chloride Substances 0.000 claims description 7
• WQZGKKKJIJFFOK-VFUOTHLCSA-N β-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 7
• 239000004698 Polyethylene (PE) Substances 0.000 claims description 6
• IQPQWNKOIGAROB-UHFFFAOYSA-N [N-]=C=O Chemical compound [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 6
• 150000001299 aldehydes Chemical class 0.000 claims description 6
• 229910052783 alkali metal Inorganic materials 0.000 claims description 6
• 239000004202 carbamide Substances 0.000 claims description 6
• 239000004715 ethylene vinyl alcohol Substances 0.000 claims description 6
• 229920001519 homopolymer Polymers 0.000 claims description 6
• 229920000573 polyethylene Polymers 0.000 claims description 6
• WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-butanediol Substances OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 5
• 239000001913 cellulose Substances 0.000 claims description 5
• 229920002678 cellulose Polymers 0.000 claims description 5
• 239000000594 mannitol Substances 0.000 claims description 5
• 235000010355 mannitol Nutrition 0.000 claims description 5
• 239000000178 monomer Substances 0.000 claims description 5
• 229920000223 polyglycerol Polymers 0.000 claims description 5
• PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 5
• YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 4
• 239000004970 Chain extender Substances 0.000 claims description 4
• 239000004952 Polyamide Substances 0.000 claims description 4
• ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 4
• 150000007513 acids Chemical class 0.000 claims description 4
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
• 239000007795 chemical reaction product Substances 0.000 claims description 4
• VOLSCWDWGMWXGO-UHFFFAOYSA-N cyclobuten-1-yl acetate Chemical compound CC(=O)OC1=CCC1 VOLSCWDWGMWXGO-UHFFFAOYSA-N 0.000 claims description 4
• 150000002118 epoxides Chemical class 0.000 claims description 4
• 150000002170 ethers Chemical class 0.000 claims description 4
• 239000005038 ethylene vinyl acetate Substances 0.000 claims description 4
• 150000002513 isocyanates Chemical class 0.000 claims description 4
• 150000002895 organic esters Chemical class 0.000 claims description 4
• 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 4
• 229920002647 polyamide Polymers 0.000 claims description 4
• 229920000856 Amylose Polymers 0.000 claims description 3
• 229920002301 Cellulose acetate Polymers 0.000 claims description 3
• 229920000881 Modified starch Polymers 0.000 claims description 3
• 239000004368 Modified starch Substances 0.000 claims description 3
• 150000008064 anhydrides Chemical class 0.000 claims description 3
• 150000001991 dicarboxylic acids Chemical class 0.000 claims description 3
• 150000002009 diols Chemical group 0.000 claims description 3
• 150000004676 glycans Polymers 0.000 claims description 3
• 150000002485 inorganic esters Chemical class 0.000 claims description 3
• 235000019426 modified starch Nutrition 0.000 claims description 3
• IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-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
• 229920001223 polyethylene glycol Polymers 0.000 claims description 3
• 229920002959 polymer blend Polymers 0.000 claims description 3
• 229920001282 polysaccharide Polymers 0.000 claims description 3
• 239000005017 polysaccharide Substances 0.000 claims description 3
• 150000004804 polysaccharides Polymers 0.000 claims description 3
• DNIAPMSPPWPWGF-GSVOUGTGSA-N (-)-propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-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
• UNVGBIALRHLALK-UHFFFAOYSA-N (±)-1,5-Hexanediol Chemical compound CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 claims description 2
• ASZLNPRMVCGYCI-UHFFFAOYSA-N 1$l^{2}-azolidine Chemical group C1CC[N]C1 ASZLNPRMVCGYCI-UHFFFAOYSA-N 0.000 claims description 2
• ALQSHHUCVQOPAS-UHFFFAOYSA-N 1,5-Pentanediol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 claims description 2
• 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 description 2
• IWHLYPDWHHPVAA-UHFFFAOYSA-N 6-hydroxyhexanoic acid Chemical compound OCCCCCC(O)=O IWHLYPDWHHPVAA-UHFFFAOYSA-N 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
• KGBXLFKZBHKPEV-UHFFFAOYSA-N Boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
• 229920002134 Carboxymethyl cellulose 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
• 239000005058 Isophorone diisocyanate Substances 0.000 claims description 2
• 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 2
• 229940117969 NEOPENTYL GLYCOL Drugs 0.000 claims description 2
• 229920001228 Polyisocyanate Polymers 0.000 claims description 2
• 239000004743 Polypropylene Substances 0.000 claims description 2
• 229920001451 Polypropylene glycol Polymers 0.000 claims description 2
• 239000004793 Polystyrene Substances 0.000 claims description 2
• 239000000654 additive Substances 0.000 claims description 2
• 229920003232 aliphatic polyester Polymers 0.000 claims description 2
• 125000005157 alkyl carboxy group Chemical group 0.000 claims description 2
• 150000001412 amines Chemical class 0.000 claims description 2
• 150000001413 amino acids Chemical class 0.000 claims description 2
• 159000000032 aromatic acids Chemical class 0.000 claims description 2
• 229920001400 block copolymer Polymers 0.000 claims description 2
• 239000004327 boric acid Substances 0.000 claims description 2
• 239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
• 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 2
• 125000004181 carboxyalkyl group Chemical group 0.000 claims description 2
• 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 2
• 125000005442 diisocyanate group Chemical group 0.000 claims description 2
• QHZOMAXECYYXGP-UHFFFAOYSA-N ethene;prop-2-enoic acid Chemical compound C=C.OC(=O)C=C QHZOMAXECYYXGP-UHFFFAOYSA-N 0.000 claims description 2
• 239000000835 fiber Substances 0.000 claims description 2
• 150000002334 glycols Chemical class 0.000 claims description 2
• 229920000578 graft polymer Polymers 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
• 239000000155 melt Substances 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
• 229920000058 polyacrylate Polymers 0.000 claims description 2
• 229920000647 polyepoxide Polymers 0.000 claims description 2
• 239000005056 polyisocyanate Substances 0.000 claims description 2
• 229920000193 polymethacrylate Polymers 0.000 claims description 2
• 229920001155 polypropylene Polymers 0.000 claims description 2
• 229920002223 polystyrene Polymers 0.000 claims description 2
• 229920000166 polytrimethylene carbonate Polymers 0.000 claims description 2
• 229920002635 polyurethane Polymers 0.000 claims description 2
• 239000004814 polyurethane Substances 0.000 claims description 2
• 235000019448 polyvinylpyrrolidone-vinyl acetate copolymer Nutrition 0.000 claims description 2
• CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 claims description 2
• 239000004328 sodium tetraborate Substances 0.000 claims description 2
• 235000010339 sodium tetraborate Nutrition 0.000 claims description 2
• 150000003568 thioethers Chemical class 0.000 claims description 2
• ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 claims description 2
• 229920002554 vinyl polymer Polymers 0.000 claims description 2
• 235000019422 polyvinyl alcohol Nutrition 0.000 claims 4
• FBPFZTCFMRRESA-KVTDHHQDSA-N Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
• VXXDXJJJTYQHPX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;2-ethyl-2-(hydroxymethyl)propane-1,3-diol Chemical compound CCC(CO)(CO)CO.OCC(CO)(CO)CO VXXDXJJJTYQHPX-UHFFFAOYSA-N 0.000 claims 1
• SLCVBVWXLSEKPL-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims 1
• DXGJPCOIHCEGFD-UHFFFAOYSA-N 5-isocyanato-2-(isocyanatomethyl)-5-phenylcyclohexa-1,3-diene Chemical compound C1=CC(CN=C=O)=CCC1(N=C=O)C1=CC=CC=C1 DXGJPCOIHCEGFD-UHFFFAOYSA-N 0.000 claims 1
• BUKOWKOPJSGGQK-UHFFFAOYSA-N 6-hydroxyoctanoic acid Chemical compound CCC(O)CCCCC(O)=O BUKOWKOPJSGGQK-UHFFFAOYSA-N 0.000 claims 1
• 102000003668 Destrin Human genes 0.000 claims 1
• 108090000082 Destrin Proteins 0.000 claims 1
• RRAMGCGOFNQTLD-UHFFFAOYSA-N Hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims 1
• 239000005057 Hexamethylene diisocyanate Substances 0.000 claims 1
• HOVAGTYPODGVJG-WLDMJGECSA-N Methylglucoside Chemical compound COC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HOVAGTYPODGVJG-WLDMJGECSA-N 0.000 claims 1
• 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
• 230000002378 acidificating Effects 0.000 claims 1
• 230000000996 additive Effects 0.000 claims 1
• 150000001408 amides Chemical class 0.000 claims 1
• 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
• JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 claims 1
• FYFFGSSZFBZTAH-UHFFFAOYSA-N methylaminomethanetriol Chemical compound CNC(O)(O)O FYFFGSSZFBZTAH-UHFFFAOYSA-N 0.000 claims 1
• 229920000068 poly(2-ethyl-2-oxazoline) Polymers 0.000 claims 1
• KFFMWJLUQMFKOH-UHFFFAOYSA-N pyrrol-1-ide Chemical class C=1C=C[N-]C=1 KFFMWJLUQMFKOH-UHFFFAOYSA-N 0.000 claims 1
• 238000000518 rheometry Methods 0.000 claims 1
• 159000000000 sodium salts Chemical class 0.000 claims 1
• 150000003673 urethanes Chemical class 0.000 claims 1
• 239000008188 pellet Substances 0.000 description 16
• 229910052739 hydrogen Inorganic materials 0.000 description 13
• 238000001125 extrusion Methods 0.000 description 11
• 150000001875 compounds Chemical class 0.000 description 10
• 239000001257 hydrogen Substances 0.000 description 10
• 239000004416 thermosoftening plastic Substances 0.000 description 9
• 238000000071 blow moulding Methods 0.000 description 8
• 238000002156 mixing Methods 0.000 description 8
• 210000003128 Head Anatomy 0.000 description 7
• 230000035699 permeability Effects 0.000 description 7
• 238000006065 biodegradation reaction Methods 0.000 description 6
• 238000000034 method Methods 0.000 description 6
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
• 238000007792 addition Methods 0.000 description 5
• 235000014113 dietary fatty acids Nutrition 0.000 description 5
• 239000000194 fatty acid Substances 0.000 description 5
• 238000004519 manufacturing process Methods 0.000 description 5
• 239000000126 substance Substances 0.000 description 5
• BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-Methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 4
• JUJWROOIHBZHMG-UHFFFAOYSA-O Pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 4
• 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
• 125000000217 alkyl group Chemical group 0.000 description 4
• 238000007872 degassing Methods 0.000 description 4
• 150000004665 fatty acids Chemical class 0.000 description 4
• 201000002113 hereditary lymphedema I Diseases 0.000 description 4
• UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
• 125000004435 hydrogen atoms Chemical group [H]* 0.000 description 4
• 238000001746 injection moulding Methods 0.000 description 4
• 238000002360 preparation method Methods 0.000 description 4
• 150000003839 salts Chemical class 0.000 description 4
• YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
• 229920002521 Macromolecule Polymers 0.000 description 3
• 240000008042 Zea mays Species 0.000 description 3
• QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
• 150000001340 alkali metals Chemical class 0.000 description 3
• 125000003277 amino group Chemical group 0.000 description 3
• QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
• 238000007906 compression Methods 0.000 description 3
• 238000007334 copolymerization reaction Methods 0.000 description 3
• 238000002425 crystallisation Methods 0.000 description 3
• 230000005712 crystallization Effects 0.000 description 3
• 150000002148 esters Chemical class 0.000 description 3
• 125000000524 functional group Chemical group 0.000 description 3
• AEMRFAOFKBGASW-UHFFFAOYSA-N glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 3
• 150000001261 hydroxy acids Chemical class 0.000 description 3
• 239000004615 ingredient Substances 0.000 description 3
• 239000007788 liquid Substances 0.000 description 3
• 239000000463 material Substances 0.000 description 3
• 150000002772 monosaccharides Chemical group 0.000 description 3
• 150000002892 organic cations Chemical class 0.000 description 3
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
• ZTHKPSBRWLGUIK-XORBCWOASA-N (2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-6-[[(2R,3S,4R,5R,6R)-3-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2R,3S,4R Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)O[C@H](OC[C@@H]2[C@H]([C@H](O)[C@@H](O)[C@@H](O[C@@H]3[C@H](O[C@H](O[C@@H]4[C@H](O[C@H](O)[C@H](O)[C@H]4O)CO)[C@H](O)[C@H]3O)CO)O2)O[C@@H]2[C@@H]([C@@H](O)[C@H](O[C@@H]3[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)[C@@H](CO)O2)O)[C@H](O)[C@H]1O ZTHKPSBRWLGUIK-XORBCWOASA-N 0.000 description 2
• WXZMFSXDPGVJKK-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
• UPMLOUAZCHDJJD-UHFFFAOYSA-N Diphenylmethane p,p'-diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
• DPUOLQHDNGRHBS-KTKRTIGZSA-N Erucic acid Chemical class CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 2
• BJHIKXHVCXFQLS-UYFOZJQFSA-N Fructose Natural products OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 description 2
• FPYJFEHAWHCUMM-UHFFFAOYSA-N Maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
• TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
• ZQPPMHVWECSIRJ-KTKRTIGZSA-N Oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
• IPCSVZSSVZVIGE-UHFFFAOYSA-N Palmitic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
• PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 2
• SRBFZHDQGSBBOR-SQOUGZDYSA-N Xylose Natural products O[C@@H]1CO[C@@H](O)[C@@H](O)[C@@H]1O SRBFZHDQGSBBOR-SQOUGZDYSA-N 0.000 description 2
• 230000002745 absorbent Effects 0.000 description 2
• 239000002250 absorbent Substances 0.000 description 2
• 238000010521 absorption reaction Methods 0.000 description 2
• 229920000615 alginic acid Polymers 0.000 description 2
• 235000010443 alginic acid Nutrition 0.000 description 2
• 150000001342 alkaline earth metals Chemical class 0.000 description 2
• 229920002988 biodegradable polymer Polymers 0.000 description 2
• 239000004621 biodegradable polymer Substances 0.000 description 2
• 229910052796 boron Inorganic materials 0.000 description 2
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