ES2297399T3 - Esteres de carboxialquilcelulosa de peso molecular bajo y su uso como aglomerantes de baja viscosidad y modificadores en composiciones de revestimiento. - Google Patents
Esteres de carboxialquilcelulosa de peso molecular bajo y su uso como aglomerantes de baja viscosidad y modificadores en composiciones de revestimiento. Download PDFInfo
- Publication number
- ES2297399T3 ES2297399T3 ES04719734T ES04719734T ES2297399T3 ES 2297399 T3 ES2297399 T3 ES 2297399T3 ES 04719734 T ES04719734 T ES 04719734T ES 04719734 T ES04719734 T ES 04719734T ES 2297399 T3 ES2297399 T3 ES 2297399T3
- Authority
- ES
- Spain
- Prior art keywords
- ester
- cellulose
- carboxyalkyl
- weight
- degree
- 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.)
- Expired - Lifetime
Links
- 239000008199 coating composition Substances 0.000 title claims description 44
- 239000011230 binding agent Substances 0.000 title abstract description 8
- 239000003607 modifier Substances 0.000 title description 3
- 150000002148 esters Chemical class 0.000 claims abstract description 224
- 229920002678 cellulose Polymers 0.000 claims abstract description 172
- 239000001913 cellulose Substances 0.000 claims abstract description 131
- 239000000203 mixture Substances 0.000 claims abstract description 94
- 238000000576 coating method Methods 0.000 claims abstract description 58
- 229920005989 resin Polymers 0.000 claims abstract description 25
- 239000011347 resin Substances 0.000 claims abstract description 25
- 239000003960 organic solvent Substances 0.000 claims abstract description 16
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 107
- 238000006467 substitution reaction Methods 0.000 claims description 101
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 93
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 92
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 92
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 92
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 57
- 239000002253 acid Substances 0.000 claims description 52
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 52
- -1 hydroxyl anhydroglucose Chemical compound 0.000 claims description 49
- 239000002904 solvent Substances 0.000 claims description 45
- 239000003795 chemical substances by application Substances 0.000 claims description 42
- 239000000049 pigment Substances 0.000 claims description 37
- 239000011248 coating agent Substances 0.000 claims description 36
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 31
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 claims description 28
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 27
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 27
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims description 27
- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 claims description 27
- 229920000642 polymer Polymers 0.000 claims description 21
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 15
- 229920000877 Melamine resin Polymers 0.000 claims description 13
- 239000006185 dispersion Substances 0.000 claims description 12
- 229920002635 polyurethane Polymers 0.000 claims description 11
- 239000004814 polyurethane Substances 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 10
- 229920000728 polyester Polymers 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- 239000004952 Polyamide Substances 0.000 claims description 8
- AVMNFQHJOOYCAP-UHFFFAOYSA-N acetic acid;propanoic acid Chemical compound CC(O)=O.CCC(O)=O AVMNFQHJOOYCAP-UHFFFAOYSA-N 0.000 claims description 8
- 229920000180 alkyd Polymers 0.000 claims description 8
- 229920002647 polyamide Polymers 0.000 claims description 8
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 7
- 239000003822 epoxy resin Substances 0.000 claims description 7
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 7
- 229920000647 polyepoxide Polymers 0.000 claims description 7
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 6
- 238000000926 separation method Methods 0.000 claims description 6
- 239000006096 absorbing agent Substances 0.000 claims description 5
- 239000007900 aqueous suspension Substances 0.000 claims description 5
- 239000000417 fungicide Substances 0.000 claims description 5
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 claims description 5
- 238000000518 rheometry Methods 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- LDMRLRNXHLPZJN-UHFFFAOYSA-N 3-propoxypropan-1-ol Chemical compound CCCOCCCO LDMRLRNXHLPZJN-UHFFFAOYSA-N 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 229920006397 acrylic thermoplastic Polymers 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 238000004581 coalescence Methods 0.000 claims description 4
- 230000007797 corrosion Effects 0.000 claims description 4
- 238000005260 corrosion Methods 0.000 claims description 4
- 239000002270 dispersing agent Substances 0.000 claims description 4
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000003112 inhibitor Substances 0.000 claims description 4
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 4
- 239000005056 polyisocyanate Substances 0.000 claims description 4
- 229920001228 polyisocyanate Polymers 0.000 claims description 4
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 238000009736 wetting Methods 0.000 claims description 4
- 239000000080 wetting agent Substances 0.000 claims description 4
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 claims description 3
- 239000013036 UV Light Stabilizer Substances 0.000 claims description 3
- 230000003254 anti-foaming effect Effects 0.000 claims description 3
- 238000004040 coloring Methods 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- MCSINKKTEDDPNK-UHFFFAOYSA-N propyl propionate Chemical compound CCCOC(=O)CC MCSINKKTEDDPNK-UHFFFAOYSA-N 0.000 claims description 3
- 230000005855 radiation Effects 0.000 claims description 3
- 230000008719 thickening Effects 0.000 claims description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 239000010445 mica Substances 0.000 claims description 2
- 229910052618 mica group Inorganic materials 0.000 claims description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims 9
- BTMVHUNTONAYDX-UHFFFAOYSA-N butyl propionate Chemical compound CCCCOC(=O)CC BTMVHUNTONAYDX-UHFFFAOYSA-N 0.000 claims 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- 230000000087 stabilizing effect Effects 0.000 claims 2
- 238000006116 polymerization reaction Methods 0.000 abstract description 36
- 229920006217 cellulose acetate butyrate Polymers 0.000 abstract description 5
- 229920008347 Cellulose acetate propionate Polymers 0.000 abstract description 4
- 239000006254 rheological additive Substances 0.000 abstract description 4
- 239000000976 ink Substances 0.000 abstract description 3
- 235000010980 cellulose Nutrition 0.000 description 63
- 239000007787 solid Substances 0.000 description 56
- 239000000243 solution Substances 0.000 description 48
- 238000000034 method Methods 0.000 description 43
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 39
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 37
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 33
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 29
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- 238000006460 hydrolysis reaction Methods 0.000 description 24
- 230000007062 hydrolysis Effects 0.000 description 23
- UGZICOVULPINFH-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O UGZICOVULPINFH-UHFFFAOYSA-N 0.000 description 20
- 239000000047 product Substances 0.000 description 20
- 239000000523 sample Substances 0.000 description 20
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 16
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 13
- 229960000583 acetic acid Drugs 0.000 description 13
- 229920002301 cellulose acetate Polymers 0.000 description 13
- 239000000126 substance Substances 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 10
- 229910052782 aluminium Inorganic materials 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- 238000009472 formulation Methods 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 8
- 238000009826 distribution Methods 0.000 description 8
- 238000005227 gel permeation chromatography Methods 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 7
- 239000002585 base Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 230000007547 defect Effects 0.000 description 7
- 238000005886 esterification reaction Methods 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 125000004185 ester group Chemical group 0.000 description 6
- 230000032050 esterification Effects 0.000 description 6
- BHXIWUJLHYHGSJ-UHFFFAOYSA-N ethyl 3-ethoxypropanoate Chemical compound CCOCCC(=O)OCC BHXIWUJLHYHGSJ-UHFFFAOYSA-N 0.000 description 6
- 238000004817 gas chromatography Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229910052751 metal Chemical class 0.000 description 6
- 239000002184 metal Chemical class 0.000 description 6
- 229920001542 oligosaccharide Polymers 0.000 description 6
- 150000007524 organic acids Chemical class 0.000 description 6
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 5
- 229920013820 alkyl cellulose Polymers 0.000 description 5
- 150000008064 anhydrides Chemical class 0.000 description 5
- 150000001720 carbohydrates Chemical class 0.000 description 5
- 239000003431 cross linking reagent Substances 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 239000000499 gel Substances 0.000 description 5
- 150000004676 glycans Chemical class 0.000 description 5
- 150000007974 melamines Chemical class 0.000 description 5
- 229920001282 polysaccharide Polymers 0.000 description 5
- 239000005017 polysaccharide Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- YEYKMVJDLWJFOA-UHFFFAOYSA-N 2-propoxyethanol Chemical compound CCCOCCO YEYKMVJDLWJFOA-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 238000001514 detection method Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229940093915 gynecological organic acid Drugs 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 235000005985 organic acids Nutrition 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 230000036961 partial effect Effects 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 description 3
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 3
- 229920002284 Cellulose triacetate Polymers 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920001131 Pulp (paper) Polymers 0.000 description 3
- 238000005852 acetolysis reaction Methods 0.000 description 3
- 230000021736 acetylation Effects 0.000 description 3
- 238000006640 acetylation reaction Methods 0.000 description 3
- 239000003377 acid catalyst Substances 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 3
- 230000003542 behavioural effect Effects 0.000 description 3
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 3
- YHASWHZGWUONAO-UHFFFAOYSA-N butanoyl butanoate Chemical compound CCCC(=O)OC(=O)CCC YHASWHZGWUONAO-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 230000006196 deacetylation Effects 0.000 description 3
- 238000003381 deacetylation reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- XKPKPGCRSHFTKM-UHFFFAOYSA-L magnesium;diacetate;tetrahydrate Chemical compound O.O.O.O.[Mg+2].CC([O-])=O.CC([O-])=O XKPKPGCRSHFTKM-UHFFFAOYSA-L 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 150000002482 oligosaccharides Chemical class 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 3
- 239000011877 solvent mixture Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 3
- 239000012855 volatile organic compound Substances 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- ZAXXZBQODQDCOW-UHFFFAOYSA-N 1-methoxypropyl acetate Chemical compound CCC(OC)OC(C)=O ZAXXZBQODQDCOW-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- LTEQMZWBSYACLV-UHFFFAOYSA-N Hexylbenzene Chemical compound CCCCCCC1=CC=CC=C1 LTEQMZWBSYACLV-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- 206010039509 Scab Diseases 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- ORILYTVJVMAKLC-UHFFFAOYSA-N adamantane Chemical compound C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 2
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 238000011088 calibration curve Methods 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 238000004590 computer program Methods 0.000 description 2
- PGRHXDWITVMQBC-UHFFFAOYSA-N dehydroacetic acid Chemical compound CC(=O)C1C(=O)OC(C)=CC1=O PGRHXDWITVMQBC-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 150000002016 disaccharides Chemical class 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 2
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 229940097364 magnesium acetate tetrahydrate Drugs 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 239000003550 marker Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 230000008823 permeabilization Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000012488 sample solution Substances 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000010189 synthetic method Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- ARVUDIQYNJVQIW-UHFFFAOYSA-N (4-dodecoxy-2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC(OCCCCCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 ARVUDIQYNJVQIW-UHFFFAOYSA-N 0.000 description 1
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-UHFFFAOYSA-N 0.000 description 1
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 description 1
- LHJGJYXLEPZJPM-UHFFFAOYSA-N 2,4,5-trichlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C=C1Cl LHJGJYXLEPZJPM-UHFFFAOYSA-N 0.000 description 1
- JLZIIHMTTRXXIN-UHFFFAOYSA-N 2-(2-hydroxy-4-methoxybenzoyl)benzoic acid Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1C(O)=O JLZIIHMTTRXXIN-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical group COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- VJMGCRKBPXGKAH-UHFFFAOYSA-N 3,4,4-trimethyl-1,3-oxazolidine Chemical compound CN1COCC1(C)C VJMGCRKBPXGKAH-UHFFFAOYSA-N 0.000 description 1
- CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical group COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 1
- GUQMDNQYMMRJPY-UHFFFAOYSA-N 4,4-dimethyl-1,3-oxazolidine Chemical compound CC1(C)COCN1 GUQMDNQYMMRJPY-UHFFFAOYSA-N 0.000 description 1
- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 1
- ZPQAKYPOZRXKFA-UHFFFAOYSA-N 6-Undecanone Chemical compound CCCCCC(=O)CCCCC ZPQAKYPOZRXKFA-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 229920002749 Bacterial cellulose Polymers 0.000 description 1
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 1
- VCTDPGDVDBXMNJ-UHFFFAOYSA-N CCC(CC)(C(C=C1C(C)=O)=CC=C1O)OP(O)=O Chemical compound CCC(CC)(C(C=C1C(C)=O)=CC=C1O)OP(O)=O VCTDPGDVDBXMNJ-UHFFFAOYSA-N 0.000 description 1
- VPFNWSAQNWQCNX-UHFFFAOYSA-N CCCCCCCCCCCCC[Na] Chemical compound CCCCCCCCCCCCC[Na] VPFNWSAQNWQCNX-UHFFFAOYSA-N 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- 239000004287 Dehydroacetic acid Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 241000220010 Rhode Species 0.000 description 1
- OSOSMTZOKLTVFS-UHFFFAOYSA-N S(=O)(=O)(O)C(C(=O)O)CC(=O)O.C(C)C(C[Na])CCCC Chemical compound S(=O)(=O)(O)C(C(=O)O)CC(=O)O.C(C)C(C[Na])CCCC OSOSMTZOKLTVFS-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- HVQNXRAMOIQYMZ-UHFFFAOYSA-N acetic acid;1-butoxybutane;ethane-1,2-diol Chemical compound CC(O)=O.OCCO.CCCCOCCCC HVQNXRAMOIQYMZ-UHFFFAOYSA-N 0.000 description 1
- QWPDCOWMNSWKIQ-UHFFFAOYSA-N acetic acid;hexane-1,2-diol Chemical group CC(O)=O.CCCCC(O)CO QWPDCOWMNSWKIQ-UHFFFAOYSA-N 0.000 description 1
- YJVBLROMQZEFPA-UHFFFAOYSA-L acid red 26 Chemical compound [Na+].[Na+].CC1=CC(C)=CC=C1N=NC1=C(O)C(S([O-])(=O)=O)=CC2=CC(S([O-])(=O)=O)=CC=C12 YJVBLROMQZEFPA-UHFFFAOYSA-L 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- WPKYZIPODULRBM-UHFFFAOYSA-N azane;prop-2-enoic acid Chemical compound N.OC(=O)C=C WPKYZIPODULRBM-UHFFFAOYSA-N 0.000 description 1
- 239000005016 bacterial cellulose Substances 0.000 description 1
- QBLDFAIABQKINO-UHFFFAOYSA-N barium borate Chemical class [Ba+2].[O-]B=O.[O-]B=O QBLDFAIABQKINO-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- 229960004217 benzyl alcohol Drugs 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- RUJILUJOOCOSRO-UNLXIWHUSA-N cellooctaose 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](O[C@@H]2[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]5[C@H](O[C@@H](O[C@@H]6[C@H](O[C@@H](O[C@@H]7[C@H](O[C@@H](O)[C@H](O)[C@H]7O)CO)[C@H](O)[C@H]6O)CO)[C@H](O)[C@H]5O)CO)[C@H](O)[C@H]4O)CO)[C@H](O)[C@H]3O)CO)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O RUJILUJOOCOSRO-UNLXIWHUSA-N 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- VNZQQAVATKSIBR-UHFFFAOYSA-L copper;octanoate Chemical compound [Cu+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O VNZQQAVATKSIBR-UHFFFAOYSA-L 0.000 description 1
- JXGWDGNWDNGFJB-UHFFFAOYSA-L copper;quinoline-8-carboxylate Chemical compound [Cu+2].C1=CN=C2C(C(=O)[O-])=CC=CC2=C1.C1=CN=C2C(C(=O)[O-])=CC=CC2=C1 JXGWDGNWDNGFJB-UHFFFAOYSA-L 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 235000019258 dehydroacetic acid Nutrition 0.000 description 1
- 229940061632 dehydroacetic acid Drugs 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 239000003398 denaturant Substances 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000002320 enamel (paints) Substances 0.000 description 1
- 239000002702 enteric coating Substances 0.000 description 1
- 238000009505 enteric coating Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- CKFGINPQOCXMAZ-UHFFFAOYSA-N formaldehyde hydrate Natural products OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229960001031 glucose Drugs 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229920005684 linear copolymer Polymers 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 239000004306 orthophenyl phenol Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 150000002976 peresters Chemical group 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- TVPFLPJBESCUKI-UHFFFAOYSA-M potassium;n,n-dimethylcarbamodithioate Chemical compound [K+].CN(C)C([S-])=S TVPFLPJBESCUKI-UHFFFAOYSA-M 0.000 description 1
- QDESFMLRHRZCSV-UHFFFAOYSA-M potassium;n-(hydroxymethyl)-n-methylcarbamodithioate Chemical compound [K+].OCN(C)C([S-])=S QDESFMLRHRZCSV-UHFFFAOYSA-M 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- GDESWOTWNNGOMW-UHFFFAOYSA-N resorcinol monobenzoate Chemical compound OC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 GDESWOTWNNGOMW-UHFFFAOYSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- UMEWSJNRBXKWKZ-UHFFFAOYSA-M sodium;1,4-dioxo-1,4-dipentoxybutane-2-sulfonate Chemical compound [Na+].CCCCCOC(=O)CC(S([O-])(=O)=O)C(=O)OCCCCC UMEWSJNRBXKWKZ-UHFFFAOYSA-M 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010959 steel Substances 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
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 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 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 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
- C08B3/00—Preparation of cellulose esters of organic acids
- C08B3/16—Preparation of mixed organic cellulose esters, e.g. cellulose aceto-formate or cellulose aceto-propionate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B13/00—Preparation of cellulose ether-esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B3/00—Preparation of cellulose esters of organic acids
- C08B3/16—Preparation of mixed organic cellulose esters, e.g. cellulose aceto-formate or cellulose aceto-propionate
- C08B3/18—Aceto-butyrates
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/64—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63
- C08G18/6484—Polysaccharides and derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D101/00—Coating compositions based on cellulose, modified cellulose, or cellulose derivatives
- C09D101/08—Cellulose derivatives
- C09D101/10—Esters of organic acids
- C09D101/14—Mixed esters, e.g. cellulose acetate-butyrate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/10—Esters of organic acids, i.e. acylates
- C08L1/14—Mixed esters, e.g. cellulose acetate-butyrate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/32—Cellulose ether-esters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31703—Next to cellulosic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31975—Of cellulosic next to another carbohydrate
- Y10T428/31978—Cellulosic next to another cellulosic
- Y10T428/31982—Wood or paper
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Wood Science & Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Paper (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45503303P | 2003-03-14 | 2003-03-14 | |
| US455033P | 2003-03-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2297399T3 true ES2297399T3 (es) | 2008-05-01 |
Family
ID=33029945
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES04719734T Expired - Lifetime ES2297399T3 (es) | 2003-03-14 | 2004-03-11 | Esteres de carboxialquilcelulosa de peso molecular bajo y su uso como aglomerantes de baja viscosidad y modificadores en composiciones de revestimiento. |
Country Status (9)
| Country | Link |
|---|---|
| US (4) | US7893138B2 (enExample) |
| EP (3) | EP1603952B1 (enExample) |
| JP (3) | JP2006520420A (enExample) |
| CN (3) | CN1761685A (enExample) |
| AT (1) | ATE378357T1 (enExample) |
| DE (1) | DE602004010077T2 (enExample) |
| ES (1) | ES2297399T3 (enExample) |
| PL (1) | PL1603953T3 (enExample) |
| WO (2) | WO2004083254A1 (enExample) |
Families Citing this family (87)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8124676B2 (en) | 2003-03-14 | 2012-02-28 | Eastman Chemical Company | Basecoat coating compositions comprising low molecular weight cellulose mixed esters |
| US8461234B2 (en) | 2003-03-14 | 2013-06-11 | Eastman Chemical Company | Refinish coating compositions comprising low molecular weight cellulose mixed esters |
| US8039531B2 (en) * | 2003-03-14 | 2011-10-18 | Eastman Chemical Company | Low molecular weight cellulose mixed esters and their use as low viscosity binders and modifiers in coating compositions |
| US7893138B2 (en) * | 2003-03-14 | 2011-02-22 | Eastman Chemical Company | Low molecular weight carboxyalkylcellulose esters and their use as low viscosity binders and modifiers in coating compositions |
| US7442730B2 (en) * | 2003-11-28 | 2008-10-28 | Daicel Chemical Industries, Ltd. | Composition having disperse system, and process for producing colored organic solid particle |
| EP1689787A2 (en) | 2003-11-28 | 2006-08-16 | Eastman Chemical Company | Cellulose interpolymers and method of oxidation |
| WO2005087289A1 (ja) * | 2004-03-15 | 2005-09-22 | Terumo Kabushiki Kaisha | 癒着防止材 |
| WO2005094366A2 (en) * | 2004-03-30 | 2005-10-13 | Automotive Systems Laboratory, Inc. | Gas generating system |
| JP2006243688A (ja) * | 2005-02-01 | 2006-09-14 | Fuji Photo Film Co Ltd | セルロースアシレート光学フィルムおよびその製造方法 |
| WO2007008959A2 (en) * | 2005-07-11 | 2007-01-18 | Wood Coatings Research Group, Inc. | Aqueous dispersions utilizing carboxyalkyl cellulose esters and water reducible polymers |
| US7932309B2 (en) * | 2005-11-04 | 2011-04-26 | Hercules Incorporated | Ether derivatives of raw cotton linters for water-borne coatings |
| US20080090960A1 (en) * | 2006-09-18 | 2008-04-17 | Eastman Chemical Company | Low voc coating compositions comprising low molecular weight cellulose mixed esters and low molecular weight hydroxyl-containing polymers |
| US20080069963A1 (en) * | 2006-09-18 | 2008-03-20 | Eastman Chemical Company | Process for making low voc coating compositions comprising low molecular weight cellulose mixed esters and low molecular weight hydroxy-containing polymers |
| US9834516B2 (en) * | 2007-02-14 | 2017-12-05 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom |
| US10174129B2 (en) | 2007-02-14 | 2019-01-08 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom |
| US7919631B2 (en) * | 2007-02-14 | 2011-04-05 | Eastman Chemical Company | Production of ionic liquids |
| WO2009011228A1 (ja) * | 2007-07-19 | 2009-01-22 | Konica Minolta Opto, Inc. | セルロースエステルフィルム、セルロースエステルフィルムの製造方法、それを用いた偏光板、及び液晶表示装置 |
| EP2185596B1 (en) * | 2007-08-24 | 2018-06-13 | Eastman Chemical Company | Mixed cellulose esters having low bifringence and films made therefrom |
| US8349921B2 (en) | 2007-08-24 | 2013-01-08 | Eastman Chemical Company | Mixed cellulose ester films having +C plate and −A plate optical properties |
| US9174879B2 (en) * | 2007-11-30 | 2015-11-03 | Corning Incorporated | Ceramic precursor batch composition and method of increasing ceramic precursor batch extrusion rate |
| US8158777B2 (en) | 2008-02-13 | 2012-04-17 | Eastman Chemical Company | Cellulose esters and their production in halogenated ionic liquids |
| US9777074B2 (en) | 2008-02-13 | 2017-10-03 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom |
| US8354525B2 (en) | 2008-02-13 | 2013-01-15 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom |
| US8188267B2 (en) | 2008-02-13 | 2012-05-29 | Eastman Chemical Company | Treatment of cellulose esters |
| JP2010241848A (ja) * | 2009-03-31 | 2010-10-28 | Fujifilm Corp | セルロース樹脂組成物、成形体及び電気電子機器用筺体 |
| JP5371473B2 (ja) * | 2008-06-30 | 2013-12-18 | 富士フイルム株式会社 | セルロース誘導体、樹脂組成物、成形体並びに電気・電子機器用筺体 |
| CN102076718B (zh) * | 2008-06-30 | 2013-10-23 | 富士胶片株式会社 | 纤维素衍生物及其制备方法、纤维素树脂组合物、模制物及其制备方法、以及电气和电子设备外壳 |
| MX2011001517A (es) * | 2008-09-15 | 2011-03-29 | Eastman Chem Co | Composiciones de recubrimiento base que comprenden esteres mezclados de celulosa de bajo peso molecular. |
| WO2010085569A1 (en) * | 2009-01-21 | 2010-07-29 | Biosphere Industries, Llc | Moisture resistant coating |
| US8067488B2 (en) | 2009-04-15 | 2011-11-29 | Eastman Chemical Company | Cellulose solutions comprising tetraalkylammonium alkylphosphate and products produced therefrom |
| US9200147B2 (en) | 2010-06-29 | 2015-12-01 | Eastman Chemical Company | Processes for making cellulose ester compositions |
| US9273195B2 (en) | 2010-06-29 | 2016-03-01 | Eastman Chemical Company | Tires comprising cellulose ester/elastomer compositions |
| CN101942113A (zh) * | 2010-08-18 | 2011-01-12 | 北京理工大学 | 羧甲基纤维素硝酸酯水性分散体及其制备方法 |
| CN102675964B (zh) * | 2011-02-02 | 2014-09-03 | 日本特殊陶业株式会社 | 油墨及设备 |
| JP5689081B2 (ja) * | 2011-02-02 | 2015-03-25 | 日本特殊陶業株式会社 | インク及びデバイス |
| US8808464B2 (en) | 2011-02-15 | 2014-08-19 | Ecolab Usa Inc. | Method for removal of a hydrophobic and particulate soil composition |
| US8349782B2 (en) | 2011-02-15 | 2013-01-08 | Ecolab Usa Inc. | Hydrophobic and particulate soil removal composition |
| US9796791B2 (en) | 2011-04-13 | 2017-10-24 | Eastman Chemical Company | Cellulose ester optical films |
| CN103635544B (zh) * | 2011-07-06 | 2016-09-28 | 巴斯夫涂料有限公司 | 制备赋予色彩和/或效果多层漆层的方法 |
| US8691893B2 (en) * | 2011-10-07 | 2014-04-08 | Masdar Institute Of Science And Technology | Biodegradable composite materials |
| EP2788385A4 (en) * | 2011-12-05 | 2015-08-12 | Resene Paints Ltd | ORGANIC CONNECTIONS |
| US20130150495A1 (en) | 2011-12-07 | 2013-06-13 | Eastman Chemical Company | Process for dispersing cellulose esters into elastomeric compositions |
| MX364278B (es) * | 2011-12-12 | 2019-04-22 | Basf Coatings Gmbh | Revestimiento de alto contenido de sólidos y proceso para revestir. |
| US9403182B2 (en) * | 2011-12-12 | 2016-08-02 | Basf Coatings Gmbh | High solids coating and process for coating |
| MX2015002430A (es) * | 2012-08-24 | 2015-06-22 | Dow Global Technologies Llc | Acetato-succinatos de hidroxialquilmetilcelulosa. |
| CN102875686A (zh) * | 2012-09-13 | 2013-01-16 | 无锡市凯利药业有限公司 | 一种醋酸丁酸纤维素的制备方法 |
| KR101967478B1 (ko) * | 2012-12-07 | 2019-08-13 | 롯데정밀화학 주식회사 | 내오염성이 개선된 아세틸화 셀룰로오스 에테르의 제조방법 및 이로부터 얻은 아세틸화 셀룰로오스 에테르 |
| CN104277122B (zh) * | 2013-07-11 | 2016-08-10 | 南通醋酸纤维有限公司 | 溶于丙酮的纤维素酯的直接合成方法及其产品 |
| CN103421413B (zh) * | 2013-08-23 | 2015-11-25 | 苏州长盛机电有限公司 | 一种防盗门金属面板涂料 |
| EP2868716B1 (en) | 2013-11-04 | 2017-01-04 | Omya International AG | Process for producing a high solids pigment suspension comprising carboxymethylcellulose-based dispersant |
| CN104447956A (zh) * | 2014-11-14 | 2015-03-25 | 陕西天瑞生物科技有限公司 | 聚氨酯界面特异性亲和多肽及其筛选方法 |
| JP2016183278A (ja) * | 2015-03-26 | 2016-10-20 | 富士ゼロックス株式会社 | 樹脂組成物、樹脂成形体の製造方法、及び樹脂成形体 |
| CN105440141B (zh) * | 2015-11-12 | 2018-01-09 | 中山大桥化工集团有限公司 | 一种乙酰基丁酰基纤维素的制备方法 |
| JP6440149B2 (ja) * | 2016-01-18 | 2018-12-19 | 旭化成株式会社 | セルロース製剤 |
| US10077343B2 (en) | 2016-01-21 | 2018-09-18 | Eastman Chemical Company | Process to produce elastomeric compositions comprising cellulose ester additives |
| JP2017171854A (ja) * | 2016-03-25 | 2017-09-28 | 富士ゼロックス株式会社 | 樹脂組成物、樹脂成形体、及び樹脂組成物の製造方法 |
| CN107254004A (zh) * | 2017-01-20 | 2017-10-17 | 北京理工大学 | 羧甲基纤维素醋酸丙酸酯及其制备方法和用途 |
| JP2020511572A (ja) * | 2017-03-17 | 2020-04-16 | ダウ グローバル テクノロジーズ エルエルシー | 反応生成物混合物からのエステル化セルロースエーテルの回収方法 |
| EP3625295A4 (en) | 2017-05-15 | 2021-07-21 | Alpha Assembly Solutions Inc. | DIELECTRIC INK COMPOSITION |
| CN107576653B (zh) * | 2017-06-24 | 2023-03-17 | 中瀚利加（北京）科技有限公司 | 一种用于鉴定孕妇羊水的组合物 |
| DE102017219658A1 (de) * | 2017-11-06 | 2019-05-09 | Tesa Se | Verfahren zur Herstellung eines Klebebandes |
| JP2019099773A (ja) * | 2017-12-08 | 2019-06-24 | フジコピアン株式会社 | ウレタンエラストマーシート |
| BE1025137B1 (nl) * | 2017-12-22 | 2018-11-09 | Nutri-Ad International Nv | Diervoeder materiaal |
| CN108760900A (zh) * | 2018-03-20 | 2018-11-06 | 华南理工大学 | 一种测定羧甲基纤维素钠取代度的顶空气相色谱法 |
| CN112004895B (zh) * | 2018-04-24 | 2022-10-21 | 伊士曼(中国)投资管理有限公司 | 醇溶性印刷油墨组合物 |
| US20210244049A1 (en) | 2018-06-15 | 2021-08-12 | Taminco Bvba | Treatment of poultry or pigs for reducing the feed conversion ratio or increasing their bodyweight gain |
| CN108760961B (zh) * | 2018-08-06 | 2020-09-22 | 青岛中科荣达新材料有限公司 | 一种液相色谱法检测固体福美钾纯度的方法 |
| CN109192058B (zh) * | 2018-09-13 | 2020-10-23 | 福建省张氏新材料科技有限公司 | 一种具有应力变色效应的热转印商标及其生产工艺 |
| WO2020163259A1 (en) * | 2019-02-04 | 2020-08-13 | Eastman Chemical Company | Cellulose ester compositions derived from post-consumer tire content syngas |
| US11447576B2 (en) * | 2019-02-04 | 2022-09-20 | Eastman Chemical Company | Cellulose ester compositions derived from recycled plastic content syngas |
| US11370983B2 (en) | 2019-02-04 | 2022-06-28 | Eastman Chemical Company | Gasification of plastics and solid fossil fuels |
| JP7149885B2 (ja) * | 2019-03-22 | 2022-10-07 | 株式会社ダイセル | セルロース誘導体粒子、化粧品組成物及びセルロース誘導体粒子の製造方法 |
| CN110387028B (zh) * | 2019-05-21 | 2021-12-03 | 江南大学 | 一种羧基化纳米纤维素晶须改性水性聚氨酯的制备方法 |
| JP7291553B2 (ja) * | 2019-06-20 | 2023-06-15 | 田中貴金属工業株式会社 | 金属パターンの形成方法 |
| KR20220055479A (ko) | 2019-08-26 | 2022-05-03 | 이스트만 케미칼 컴파니 | 2-에틸헥사노일 치환된 셀룰로스 에스터 |
| WO2021061918A1 (en) * | 2019-09-27 | 2021-04-01 | Eastman Chemical Company | Cellulose ester compositions derived from recycled cellulose ester content syngas |
| WO2021068117A1 (en) * | 2019-10-08 | 2021-04-15 | Eastman Chemical (China) Co., Ltd. | Polymer compositions comprising cellulose esters |
| SE543736C2 (en) * | 2019-11-04 | 2021-07-06 | Stora Enso Oyj | Coating for reducing oil absorbency of cellulosic webs |
| EP4061864B1 (en) | 2019-11-18 | 2023-10-18 | Henkel AG & Co. KGaA | One component (1k) anaerobic curable composition |
| JP6779400B1 (ja) * | 2020-03-04 | 2020-11-04 | 大日精化工業株式会社 | 樹脂ビーズ、樹脂ビーズの製造方法、及び樹脂ビーズを用いた製品 |
| JP6872068B1 (ja) | 2020-09-01 | 2021-05-19 | 大日精化工業株式会社 | 樹脂ビーズ、樹脂ビーズの製造方法、及び樹脂ビーズを用いた製品 |
| CN112457721B (zh) * | 2020-12-03 | 2023-02-03 | 上海瑞君电泳涂料有限公司 | 环氧电泳涂料用色浆、电泳涂料及其制备工艺 |
| JP6921293B1 (ja) | 2020-12-23 | 2021-08-18 | 大日精化工業株式会社 | 樹脂ビーズ、樹脂ビーズの製造方法、及び樹脂ビーズを用いた製品 |
| GB2607074A (en) * | 2021-05-27 | 2022-11-30 | Kemira Oyj | Moisture and oil barrier |
| CN120500510A (zh) * | 2023-01-16 | 2025-08-15 | 丹尼斯科美国公司 | 新羧甲基纤维素及制备方法 |
| CN120641271A (zh) * | 2023-02-10 | 2025-09-12 | 伊士曼(中国)投资管理有限公司 | 复合纸及其制备方法 |
| CN116693703A (zh) * | 2023-07-12 | 2023-09-05 | 浦拉司科技（上海）有限责任公司 | 一种羟乙基纤维素去除金属离子的方法 |
Family Cites Families (196)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1652573A (en) | 1925-06-29 | 1927-12-13 | Mallabar Herbert John | Manufacture of cellulose acetate |
| US1683347A (en) | 1927-08-25 | 1928-09-04 | Eastman Kodak Co | Process of making chloroform-soluble cellulose acetate |
| US1878954A (en) | 1929-08-10 | 1932-09-20 | Eastman Kodak Co | Process for rendering cellulose acetate free from haze |
| US2129052A (en) | 1936-02-04 | 1938-09-06 | Eastman Kodak Co | Hydrolyzed cellulose acetate |
| US2801239A (en) * | 1954-06-07 | 1957-07-30 | Eastman Kodak Co | Method of hydrolyzing cellulose esters |
| US3281267A (en) | 1961-11-13 | 1966-10-25 | Lowe Paper Co | High gloss coated paper |
| US3386932A (en) * | 1964-06-30 | 1968-06-04 | Celanese Corp | Novel cellulosics, segmented copolymers, and methods of preparing same |
| JPS4841037B1 (enExample) * | 1964-10-26 | 1973-12-04 | ||
| US3411941A (en) | 1965-03-01 | 1968-11-19 | Eastman Kodak Co | Process for coating a metallic article with thermally reflowable cellulose acetate butyrate/melamine-formaldehyde resin/alkyd or acrylic resin coating compositions |
| US3518249A (en) * | 1966-12-01 | 1970-06-30 | Eastman Kodak Co | Oligosaccharide propionate compositions and processes |
| US3429840A (en) * | 1967-08-14 | 1969-02-25 | Eastman Kodak Co | Acrylic resins containing cellulose butyrate benzoate,coatings and compositions |
| US3850770A (en) | 1969-10-24 | 1974-11-26 | Kansai Paint Co Ltd | Radiation curable compositions from acrylurethane resins |
| US3821267A (en) * | 1970-05-05 | 1974-06-28 | Rorer Inc William H | A-acylthio-p-cyclohexylphenylacetic acid and derivatives |
| UST921011I4 (en) * | 1973-09-19 | 1974-04-09 | Defensive publication | |
| GB1463490A (en) | 1973-09-26 | 1977-02-02 | Ici Ltd | Coating process |
| UST941001I4 (en) | 1974-06-17 | 1975-12-02 | Defensive publication | |
| US3998768A (en) * | 1974-12-24 | 1976-12-21 | E. I. Du Pont De Nemours And Company | Thermosetting powder coating composition of a blend of acrylic polymers having different glass transition temperatures and a blocked polyisocyanate cross-linking agent |
| JPS51119089U (enExample) | 1975-03-22 | 1976-09-27 | ||
| JPS51119089A (en) * | 1975-04-11 | 1976-10-19 | Asahi Chem Ind Co Ltd | Method for preparing a low molecular weight cellulose mixed ester |
| JPS51119088A (en) | 1975-04-11 | 1976-10-19 | Asahi Chem Ind Co Ltd | Method for preparing a low molecular weight cellulose ester |
| US4007144A (en) * | 1976-02-27 | 1977-02-08 | Eastman Kodak Company | Thermosetting cellulose ester powder coating compositions |
| US4134809A (en) * | 1977-08-22 | 1979-01-16 | Eastman Kodak Company | Radiation curable cellulose ester-acrylate compositions |
| US4170663A (en) * | 1978-03-13 | 1979-10-09 | Ppg Industries, Inc. | Method for producing coatings of low gloss |
| JPS5676422A (en) | 1979-11-29 | 1981-06-24 | Kansai Paint Co Ltd | Cellulose derivative-containing, oxidation-curable emulsion composition |
| NZ199597A (en) | 1981-02-13 | 1985-02-28 | Dulux Australia Ltd | Acrylic coating compositions |
| DE3125569A1 (de) * | 1981-06-30 | 1983-01-20 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von ueberzuegen |
| JPS6017441B2 (ja) * | 1981-07-10 | 1985-05-02 | ダイセル化学工業株式会社 | 新規なセルロ−スアセテ−トの製造方法 |
| US4389502A (en) * | 1981-12-24 | 1983-06-21 | E. I. Du Pont De Nemours And Company | Clear air-dry acrylic lacquer coating composition |
| US4598111A (en) * | 1982-03-18 | 1986-07-01 | Glasurit America, Inc. | Coating composition containing cross-linked microparticles |
| US4725640A (en) | 1982-07-06 | 1988-02-16 | Basf Corporation | Metal fixative in automotive paint |
| DE3246417C2 (de) * | 1982-12-15 | 1987-04-09 | Akzo Gmbh, 5600 Wuppertal | Wasserunlösliche Fasern aus Celluloseacetat, Cellulosepropionat und Cellulosebutyrat mit einem extrem hohen Absorptionsvermögen für Wasser und physiologische Flüssigkeiten |
| JPS59152901A (ja) * | 1983-02-21 | 1984-08-31 | Daicel Chem Ind Ltd | カルボキシアルキル・アセチル・セルロ−スとその塩およびその製造法 |
| JPS59166501A (ja) * | 1983-03-10 | 1984-09-19 | Daicel Chem Ind Ltd | 高結晶性低分子量酢酸セルロ−ス |
| DE3322037A1 (de) * | 1983-06-18 | 1984-12-20 | Basf Farben + Fasern Ag, 2000 Hamburg | Ueberzugsmasse, insbesondere zur herstellung einer transparenten deckschicht |
| US4551491A (en) * | 1983-07-29 | 1985-11-05 | Inmont Corporation | Pearlescent automotive paint compositions |
| US4605687A (en) | 1983-08-26 | 1986-08-12 | Inmont Corporation | Multilayer automotive paint system |
| NZ209347A (en) | 1983-09-09 | 1987-06-30 | Dulux Australia Ltd | Thermoplastic coating composition containing at least one acrylic polymer and at least two plasticisers |
| US4590265A (en) * | 1984-02-17 | 1986-05-20 | Eastman Kodak Company | Carboxylated cellulose ester and manufacture thereof |
| GB2156829B (en) * | 1984-04-02 | 1987-08-19 | Kodak Ltd | Base coat compositions for wet-on-wet applicatons, and articles coated therewith |
| US4603160A (en) * | 1984-04-30 | 1986-07-29 | Eastman Kodak Company | Acrylic castings and process for the preparation thereof |
| JPS60252664A (ja) | 1984-05-28 | 1985-12-13 | Nippon Paint Co Ltd | 塗料組成物 |
| US4692481A (en) | 1984-09-27 | 1987-09-08 | E. I. Du Pont De Nemours And Company | Process for matching color of paint to a colored surface |
| US4598015A (en) | 1984-12-11 | 1986-07-01 | Inmont Corporation | Multilayer satin finish automotive paint system |
| US4551492A (en) * | 1984-12-27 | 1985-11-05 | E. I. Du Pont De Nemours And Company | Polyester coating composition |
| US4740541A (en) * | 1985-05-31 | 1988-04-26 | Borden, Inc. | Copier resistant coating for polyvinyl chloride |
| JPS61276834A (ja) | 1985-06-03 | 1986-12-06 | Nippon Oil & Fats Co Ltd | ポリウレタン樹脂成形物の上塗り塗装方法 |
| US4650821A (en) * | 1985-07-01 | 1987-03-17 | Eastman Kodak Company | Novel acrylic castings and process for the preparation thereof |
| US4598020A (en) * | 1985-08-16 | 1986-07-01 | Inmont Corporation | Automotive paint compositions containing pearlescent pigments and dyes |
| US4755581A (en) * | 1986-08-21 | 1988-07-05 | Ppg Industries, Inc. | Thermosetting high solids coating composition of epoxies, polyols and anhydrides |
| US4732790A (en) * | 1986-08-21 | 1988-03-22 | Ppg Industries, Inc. | Color plus clear application of thermosetting high solids coating composition of hydroxy-functional epoxies and anhydrides |
| US4732791A (en) * | 1986-08-21 | 1988-03-22 | Ppg Industries, Inc. | Color plus clear application of thermosetting high solids coating composition of epoxies, polyols and anhydrides |
| US4755582A (en) | 1986-08-21 | 1988-07-05 | Ppg Industries, Inc. | Thermosetting high solids coating composition of hydroxy-functional epoxies and anhydrides |
| IT1197484B (it) | 1986-10-07 | 1988-11-30 | Mazzucchelli Celluloide Spa | Procedimento per la produzione di effetti di colore a sfumatura nella massa di lastre di materiale plastico |
| US4753829A (en) * | 1986-11-19 | 1988-06-28 | Basf Corporation | Opalescent automotive paint compositions containing microtitanium dioxide pigment |
| US5089313A (en) * | 1986-12-10 | 1992-02-18 | Marley Mouldings Inc. | Process for coating metal and plastic to impart wood-like appearances |
| JPS63245478A (ja) | 1987-03-31 | 1988-10-12 | Sakura Color Prod Corp | 固形塗料 |
| EP0289997B1 (de) | 1987-05-08 | 1994-01-12 | Herberts Gesellschaft mit beschränkter Haftung | Überzugsmittel und dessen Verwendung bei Verfahren zur Herstellung von Mehrschichtüberzügen |
| US5086144A (en) | 1987-11-16 | 1992-02-04 | The Sherwin-Williams Company | Acid-functional polymers derived from cellulose acetate butyrate unsaturated alcohol copolymers and coatings prepared from same |
| US4859758A (en) | 1987-11-16 | 1989-08-22 | The Sherwin-Williams Company | Acid-functional polymers derived from cellulose ester-unsaturated alcohol copolymers, which are reacted with cyclic anhydrides |
| US4975300A (en) | 1987-12-31 | 1990-12-04 | Minnesota Mining And Manufacturing Company | Method for curing an organic coating using condensation heating and radiation energy |
| US4902578A (en) * | 1987-12-31 | 1990-02-20 | General Electric Company | Radiation-curable coating for thermoplastic substrates |
| JP2622999B2 (ja) * | 1988-01-27 | 1997-06-25 | 日本油脂 株式会社 | 有彩色金属フレーク顔料並びにこの顔料を含有する塗料組成物、インキ組成物、化粧料組成物及びプラスチック成形組成物 |
| US4855184A (en) | 1988-02-02 | 1989-08-08 | Minnesota Mining And Manufacturing Company | Radiation-curable protective coating composition |
| DE3814284A1 (de) | 1988-04-28 | 1989-11-09 | Wolff Walsrode Ag | Waessrige celluloseesterdispersionen und ihre herstellung |
| US4888372A (en) | 1988-06-23 | 1989-12-19 | E. I. Du Pont De Nemours And Company | High solids solvent-based polyester coating composition |
| US4983730A (en) * | 1988-09-02 | 1991-01-08 | Hoechst Celanese Corporation | Water soluble cellulose acetate composition having improved processability and tensile properties |
| JP2668083B2 (ja) | 1988-09-05 | 1997-10-27 | 関西ペイント株式会社 | 自動車用塗料組成物 |
| JPH02232249A (ja) * | 1989-03-03 | 1990-09-14 | Kansai Paint Co Ltd | 樹脂組成物、硬化性組成物及び塗料組成物 |
| DE3922363A1 (de) | 1989-07-07 | 1991-01-17 | Basf Lacke & Farben | Verfahren zur herstellung einer mehrschichtigen lackierung und basislack zur herstellung der basisschicht einer mehrschichtigen lackierung |
| JPH05507302A (ja) * | 1990-04-16 | 1993-10-21 | イーストマン コダック カンパニー | 低分子量セルロースエステルの製造 |
| DE4014212C2 (de) | 1990-05-03 | 1994-10-06 | Herberts Gmbh | Effektbasislack zur Beschichtung von Polypropylensubstraten |
| US6077659A (en) | 1990-05-15 | 2000-06-20 | New York Blood Center, Inc. | Vitamin E and derivatives thereof prevent potassium ion leakage and other types of damage in red cells that are virus sterilized by phthalocyanines and light |
| US5292876A (en) * | 1990-07-20 | 1994-03-08 | Eastman Kodak Company | Mixed cellulose esters |
| SG47853A1 (en) * | 1990-11-30 | 1998-04-17 | Eastman Chem Co | Aliphatic-aromatic copolyesters and cellulose ester/polymer blend |
| US5292783A (en) * | 1990-11-30 | 1994-03-08 | Eastman Kodak Company | Aliphatic-aromatic copolyesters and cellulose ester/polymer blends |
| JPH04348130A (ja) | 1991-05-24 | 1992-12-03 | Nisshinbo Ind Inc | セルロース微粉末及びその製造方法 |
| JP3208825B2 (ja) * | 1991-05-28 | 2001-09-17 | 日本油脂株式会社 | 凹凸模様を有する塗膜形成用の粉体塗料、その製造方法、製造装置、塗装方法および塗膜 |
| DE4127513A1 (de) * | 1991-08-20 | 1993-02-25 | Bayer Ag | Bindemittelgemische und ihre verwendung |
| US5283126A (en) * | 1991-08-29 | 1994-02-01 | Bee Chemical | Utilization of flexible coating on steel to impart superior scratch and chip resistance |
| US5384163A (en) * | 1991-10-23 | 1995-01-24 | Basf Corporation | Cellulose esters moidified with anhydrides of dicarboxylic acids and their use in waterborne basecoats |
| JPH0710964B2 (ja) | 1991-12-18 | 1995-02-08 | イサム塗料株式会社 | ポリウレタン塗料組成物 |
| DE4218106A1 (de) | 1992-06-02 | 1993-12-09 | Herberts Gmbh | Überzugsmittel und dessen Verwendung bei Verfahren zur Herstellung von Mehrschichtenüberzügen |
| US5425969A (en) | 1992-06-26 | 1995-06-20 | Toyota Jidosha Kabushiki Kaisha | Method of coating articles made of polypropylene with an electrically conductive primer and electrostatically applied overcoat |
| US5284885A (en) | 1992-09-29 | 1994-02-08 | Agri-Film, Inc. | Aqueous nitrocellulose compositions |
| US5873931A (en) | 1992-10-06 | 1999-02-23 | Minnesota Mining And Manufacturing Company | Coating composition having anti-reflective and anti-fogging properties |
| TW256845B (enExample) * | 1992-11-13 | 1995-09-11 | Taisyal Kagaku Kogyo Kk | |
| US5372638A (en) | 1992-11-27 | 1994-12-13 | Basf Corporation | Aluminum flake pigment treated with metal salts and coatings containing the same |
| US5360644A (en) | 1992-12-15 | 1994-11-01 | Basf Corporation | Chip-resistant composite coating |
| US6407224B1 (en) * | 1992-12-25 | 2002-06-18 | Nauchno-prozvodstvennaya firma “Efiry Tselljulosy” | Catalytic system for cellulose acylation process for producing said catalytic system, and for its practical application |
| DE4302055C1 (de) | 1993-01-26 | 1994-03-24 | Rhodia Ag Rhone Poulenc | Celluloseacetat-Filamente sowie ein Verfahren zu deren Herstellung |
| CA2116167C (en) | 1993-03-15 | 2007-05-15 | Myron W. Shaffer | One-component coating compositions containing oxime- or lactam-blocked polyisocyanates which have improved resistance to yellowing |
| US5510443A (en) * | 1993-03-15 | 1996-04-23 | Bayer Corporation | Process for preparing a coating with improved resistance to yellowing and the resulting coating |
| US6313202B1 (en) | 1993-05-28 | 2001-11-06 | Eastman Chemical Company | Cellulose ester blends |
| DE4325352C1 (de) * | 1993-07-28 | 1994-09-01 | Rhodia Ag Rhone Poulenc | Plastifiziertes Celluloseacetat, Verfahren zu dessen Herstellung und seine Verwendung zur Herstellung von Filamenten |
| US5322560A (en) * | 1993-08-31 | 1994-06-21 | Basf Corporation | Aluminum flake pigment treated with time release corrosion inhibiting compounds and coatings containing the same |
| WO1995016731A1 (en) * | 1993-12-13 | 1995-06-22 | Ppg Industries, Inc. | Coating composition and articles having a cured coating |
| JP3329049B2 (ja) | 1994-01-24 | 2002-09-30 | 日本油脂ビーエーエスエフコーティングス株式会社 | 自動車用上塗塗料のクリヤーコート用熱硬化被覆組成物 |
| US5389139A (en) * | 1994-02-14 | 1995-02-14 | Basf Corporation | Nitro-substituted polymeric corrosion inhibitors for aluminum flake pigment |
| DE4407415A1 (de) * | 1994-03-05 | 1995-09-07 | Basf Lacke & Farben | Beschichtungsmittel auf Basis eines hydroxylgruppenhaltigen Polyacrylatharzes und seine Verwendung in Verfahren zur Herstellung einer Mehrschichtlackierung |
| US5498781A (en) | 1994-05-23 | 1996-03-12 | Basf Corporation | Passification of optically variable pigment and waterborne coating compositions containg the same |
| US5520963A (en) | 1994-06-30 | 1996-05-28 | Dupont Canada, Inc. | Paint formulation |
| DE4439679A1 (de) * | 1994-11-07 | 1996-05-09 | Henkel Ecolab Gmbh & Co Ohg | Verfahren zur Herstellung von Wasch- und Reinigungsmitteltabletten durch Mikrowellen- und Heißluftbehandlung |
| US5585186A (en) | 1994-12-12 | 1996-12-17 | Minnesota Mining And Manufacturing Company | Coating composition having anti-reflective, and anti-fogging properties |
| US5527848A (en) | 1994-12-14 | 1996-06-18 | Basf Corporation | Pacification of optically variable pigments for use in waterborne coating compositions |
| CA2208273A1 (en) * | 1994-12-30 | 1996-07-11 | Kevin Joseph Edgar | Process for preparing cellulose esters using a sulfonic acid resin catalyst |
| US5705632A (en) * | 1995-01-19 | 1998-01-06 | Fuji Photo Film Co., Ltd. | Process for the preparation of cellulose acetate film |
| DE69634578T2 (de) | 1995-01-19 | 2005-09-15 | Fuji Photo Film Co., Ltd., Minami-Ashigara | Celluloseacetatlösung und Verfahren zu ihrer Herstellung |
| US5580819A (en) * | 1995-03-22 | 1996-12-03 | Ppg Industries, Inc. | Coating composition, process for producing antireflective coatings, and coated articles |
| DE69630089T2 (de) | 1995-03-31 | 2004-04-01 | Daicel Chemical Industries, Ltd., Sakai | Celluloseacetat mit hoher verformbarkeit und verfahren zu dessen herstellung |
| JP3609480B2 (ja) * | 1995-03-31 | 2005-01-12 | 大日本インキ化学工業株式会社 | 塗膜形成方法及びそれに使用されるベースコート塗料 |
| DE69626254T2 (de) | 1995-03-31 | 2003-07-24 | Daicel Chemical Industries, Ltd. | Celluloseacetat mit ausgezeichneter festigkeit und verfahren zur herstellung |
| JP3942668B2 (ja) * | 1995-03-31 | 2007-07-11 | ダイセル化学工業株式会社 | 成形性の高い酢酸セルロースおよびその製造法 |
| JP3942669B2 (ja) | 1995-03-31 | 2007-07-11 | ダイセル化学工業株式会社 | 物理強度に優れたセルロースアセテート、及びその製造法 |
| JP3533751B2 (ja) | 1995-04-26 | 2004-05-31 | 日本油脂Ｂａｓｆコーティングス株式会社 | 熱硬化性塗料組成物 |
| US6051242A (en) * | 1995-05-02 | 2000-04-18 | Mycone Dental Corporation | Quick-drying coating compositions |
| US5610233A (en) * | 1995-08-03 | 1997-03-11 | Eastman Chemical Company | Aqueous coating compositions containing cellulose esters |
| US6025433A (en) | 1995-12-20 | 2000-02-15 | Basf Coatings Ag | Thermosetting paint composition |
| US5753373A (en) * | 1995-12-21 | 1998-05-19 | Minnesota Mining And Manufacturing Company | Coating composition having anti-reflective and anti-fogging properties |
| DE19602848A1 (de) | 1996-01-26 | 1997-07-31 | Basf Ag | Verfahren zur Herstellung von Pigmenten |
| US5668273A (en) | 1996-01-29 | 1997-09-16 | Eastman Chemical Company | Carboxyalkyl cellulose esters |
| DE19609143C1 (de) * | 1996-03-08 | 1997-11-13 | Rhodia Ag Rhone Poulenc | Melt-blown-Vlies, Verfahren zu dessen Herstellung und dessen Verwendungen |
| US5998035A (en) | 1996-03-28 | 1999-12-07 | Mazda Motor Corporation | Method for forming coating and base coating paint used therefor |
| DE19616287C5 (de) | 1996-04-24 | 2013-11-14 | Eckart Gmbh | Verfahren zur Herstellung einer Perlglanzpigment-Zubereitung |
| US5741880A (en) * | 1996-05-10 | 1998-04-21 | The Sherwin-Williams Company | Clearcoating compositions |
| SE509240C2 (sv) | 1996-05-28 | 1998-12-21 | Perstorp Ab | Termoplastisk kompound bestående av en termoplastisk polymer bunden till en dendritisk eller hyperförgrenad makromolekyl samt komposition och produkt därav |
| US6046259A (en) | 1996-06-27 | 2000-04-04 | Ppg Industries Ohio, Inc. | Stable aqueous dispersions of cellulose esters and their use in coatings |
| US6040053A (en) | 1996-07-19 | 2000-03-21 | Minnesota Mining And Manufacturing Company | Coating composition having anti-reflective and anti-fogging properties |
| JP3264361B2 (ja) * | 1996-07-30 | 2002-03-11 | ダイセル化学工業株式会社 | セルロースアセテート溶液の製造方法 |
| JP4035181B2 (ja) * | 1996-07-30 | 2008-01-16 | ダイセル化学工業株式会社 | セルロースの混合脂肪酸エステル、その溶液およびセルロースの混合脂肪酸エステルフイルム |
| US6228433B1 (en) | 1997-05-02 | 2001-05-08 | Permagrain Products, Inc. | Abrasion resistant urethane coatings |
| JP3137924B2 (ja) | 1997-05-13 | 2001-02-26 | フジコピアン株式会社 | 感圧転写磁気記録媒体 |
| WO1999002619A1 (en) | 1997-07-08 | 1999-01-21 | Kansai Paint Co., Ltd. | High-solid coating composition and method of topcoating with the same |
| JPH1135601A (ja) * | 1997-07-18 | 1999-02-09 | Nippon Paper Ind Co Ltd | エステルエーテル混合セルロース誘導体及びその製造法 |
| US6001484A (en) | 1998-01-09 | 1999-12-14 | Advanced Elastomer Systems, L.P. | Composite article of cellulose esters and thermoplastic elastomers |
| US6218448B1 (en) * | 1998-04-01 | 2001-04-17 | Akzo Nobel N.V. | Mixtures or pastes based on cellulose and the use thereof in coatings |
| EP0990682B1 (en) | 1998-04-15 | 2005-11-09 | BASF Coatings Japan Ltd. | Method for formation of coating film and coating composition |
| ATE285306T1 (de) | 1998-05-15 | 2005-01-15 | Hoeganaes Ab | Metallurgische zusammensetzungen auf eisenbasis, die flussmittel enthalten und verfahren zu deren verwendung |
| US5994530A (en) | 1998-06-25 | 1999-11-30 | Eastman Chemical Corporation | Carboxyalkyl cellulose esters for use in aqueous pigment dispersions |
| DE19846971A1 (de) * | 1998-10-12 | 2000-04-20 | Basf Coatings Ag | Beschichtungsmittel, Verfahren zu seiner Herstellung und seine Verwendung als Decklack oder Klarlack, insbesondere zur Beschichtung von Kunststoffen |
| EP1048683B1 (en) * | 1998-11-13 | 2005-05-25 | DAICEL CHEMICAL INDUSTRIES, Ltd. | Aliphatic copolymer, production process, aliphatic polyester resin composition, various uses, coating composition, and agricultural or horticultural particulate composition comprising degradable coating film |
| DE19854236A1 (de) | 1998-11-24 | 2000-05-25 | Wacker Chemie Gmbh | Verwendung von Schutzkolloid-stabilisierten Vinylaromat-1,3-Dien-Mischpolymerisaten als Klebemittel für poröse Substrate |
| US6635314B1 (en) | 1999-03-17 | 2003-10-21 | E. I. Du Pont De Nemours And Company | High solids clear coating composition |
| CN1344301A (zh) | 1999-03-17 | 2002-04-10 | 纳幕尔杜邦公司 | 高固含量透明涂料组合物 |
| AU772837B2 (en) | 1999-03-17 | 2004-05-06 | E.I. Du Pont De Nemours And Company | High solids acid etch resistant clear coating composition |
| BR0010513A (pt) | 1999-03-17 | 2002-01-08 | Du Pont | Composição de revestimento transparente com alto teor de sólidos, resistente à corrosão ácida e desgastes e método de produção de um revestimento transparente em um substrato |
| US6610777B1 (en) * | 1999-07-30 | 2003-08-26 | Ppg Industries Ohio, Inc. | Flexible coating compositions having improved scratch resistance, coated substrates and methods related thereto |
| DE19936635A1 (de) * | 1999-08-04 | 2001-02-15 | Wolff Walsrode Ag | Wäßrige Überzugsmittel und dessen Verwendung in Lacken |
| JP2001129927A (ja) * | 1999-11-08 | 2001-05-15 | Konica Corp | 光学異方性フィルムおよび液晶表示装置 |
| ATE301138T1 (de) | 1999-10-27 | 2005-08-15 | Valspar Sourcing Inc | Reibfreier decklack |
| US6303670B1 (en) * | 2000-02-25 | 2001-10-16 | Nippon Paper Industries Co., Ltd. | Cellulose based coating composition curable with ultraviolet ray |
| JP3919418B2 (ja) | 2000-03-24 | 2007-05-23 | 豊田合成株式会社 | 光輝塗料及び光輝塗膜 |
| US6227433B1 (en) * | 2000-04-04 | 2001-05-08 | The Boeing Company | Friction welded fastener process |
| US6582807B2 (en) | 2000-04-07 | 2003-06-24 | Case Western Reserve University | Polymer 1D photonic crystals |
| US6653411B2 (en) | 2000-04-19 | 2003-11-25 | Brewer Science, Inc. | Anti-reflective coating compositions comprising polymerized aminoplasts |
| US6323310B1 (en) * | 2000-04-19 | 2001-11-27 | Brewer Science, Inc. | Anti-reflective coating compositions comprising polymerized aminoplasts |
| US6355303B1 (en) * | 2000-04-28 | 2002-03-12 | E. I. Du Pont De Nemours And Company | Process for the preparation of multi-layer coatings of the water-borne base coat/powder clear coat type |
| DE10048670A1 (de) | 2000-09-30 | 2002-04-25 | Basf Coatings Ag | Beschichtungsstoffsystem für die Herstellung farb- und/oder effektgebender Mehrschichtlackierungen auf der Basis von Mehrkomponentenbeschichtungsstoffen |
| DE10048849A1 (de) | 2000-10-02 | 2002-04-18 | Basf Coatings Ag | Verfahren zur Herstellung eines thermisch und mit aktinischer Strahlung härtbaren Mehrkomponentensystems und seine Verwendung |
| US6609677B2 (en) * | 2000-10-23 | 2003-08-26 | Ncr Corporation | Bevel ribbed core |
| US7026470B2 (en) | 2000-11-01 | 2006-04-11 | Eastman Chemical Corporation | Use of carboxymethyl cellulose acetate butyrate as a precoat or size for cellulosic man-made fiber boards |
| WO2001035719A2 (en) | 2000-11-02 | 2001-05-25 | Eastman Chemical Company | Wood stain containing carboxymethyl cellulose acetate butyrate |
| US20050227162A1 (en) | 2000-11-06 | 2005-10-13 | Van Rooyen Arthur Jozef Gerard | Kit of parts for the preparation of a solvent based coating composition |
| US7208534B2 (en) * | 2000-11-06 | 2007-04-24 | Akzo Nobel N.V. | Solvent based coating composition |
| DE10055549A1 (de) * | 2000-11-09 | 2002-05-29 | Basf Coatings Ag | Farb- und/oder effektgebende Mehrschichtlackierung, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE10100195A1 (de) | 2001-01-04 | 2002-08-01 | Basf Coatings Ag | Wäßriger, effektgebender Beschichtungsstoff, Verfahren zu seiner Herstellung und seine Verwendung |
| US6758992B2 (en) | 2001-02-28 | 2004-07-06 | 3M Innovative Properties Company | Process of stripe coating to produce microstructured composite articles |
| US7001948B2 (en) | 2001-05-16 | 2006-02-21 | American Polymer Corporation | Polyurea coating compositions |
| US6794442B2 (en) * | 2001-06-21 | 2004-09-21 | Basf Corporation | Fast drying basecoat refinish composition |
| DE10147546B4 (de) | 2001-09-26 | 2006-04-13 | Basf Coatings Ag | Polyurethan, Verfahren zu seiner Herstellung und seine Verwendung |
| US7446149B2 (en) * | 2001-09-27 | 2008-11-04 | Basf Corporation | Fast drying clearcoat refinish composition |
| US6522812B1 (en) * | 2001-12-19 | 2003-02-18 | Intel Corporation | Method of precision fabrication by light exposure and structure of tunable waveguide bragg grating |
| PT1483347E (pt) | 2002-02-20 | 2006-08-31 | Du Pont | Vernizes que contem copoliester-poliol altamente ramificado |
| US6924010B2 (en) * | 2002-05-08 | 2005-08-02 | Eastman Chemical Company | Low solution viscosity cellulose triacetate and its applications thereof |
| DE10241853B3 (de) * | 2002-09-09 | 2004-01-22 | Byk-Chemie Gmbh | Polymeres Harnstoffurethan als Rheologiesteuerungsmittel und Verfahren zur Herstellung |
| EP1569977B1 (en) * | 2002-11-05 | 2008-06-11 | The Sherwin-Williams Company | Curable compositions |
| US6913831B2 (en) | 2002-12-26 | 2005-07-05 | Suzuka Fuji Xerox, Co., Ltd. | Coating material for recycling and a thermoplastic resin mold |
| US8039531B2 (en) * | 2003-03-14 | 2011-10-18 | Eastman Chemical Company | Low molecular weight cellulose mixed esters and their use as low viscosity binders and modifiers in coating compositions |
| US7893138B2 (en) | 2003-03-14 | 2011-02-22 | Eastman Chemical Company | Low molecular weight carboxyalkylcellulose esters and their use as low viscosity binders and modifiers in coating compositions |
| US20040185269A1 (en) | 2003-03-18 | 2004-09-23 | Loper Scott W. | Scratch and mar resistant low VOC coating composition |
| EP1625176B1 (en) | 2003-04-24 | 2009-07-22 | Nuplex Resins B.V. | Coating composition |
| US20050031873A1 (en) | 2003-08-04 | 2005-02-10 | Guenter Berschel | Method for multi-coat refinishing of substrates |
| US7144631B2 (en) * | 2003-11-07 | 2006-12-05 | E. I. Du Pont De Nemours And Company | Method for achieving primerless windshield sealant adhesion over a carbamate clearcoat |
| US20050123781A1 (en) | 2003-12-04 | 2005-06-09 | Drescher James C. | One-component flexible etch resistant clearcoat |
| US7185530B2 (en) * | 2003-12-22 | 2007-03-06 | Eastman Chemical Company | Device to measure the solidification properties of a liquid film and method therefor |
| US7472584B2 (en) * | 2003-12-22 | 2009-01-06 | Eastman Chemical Company | Device to measure the solidification properties of a liquid film and method therefor |
| TW200530352A (en) | 2004-02-09 | 2005-09-16 | Nippon Paint Co Ltd | Metallic base coating composition and process for producing a composite film |
| US7052540B2 (en) * | 2004-03-11 | 2006-05-30 | Eastman Chemical Company | Aqueous dispersions of carboxylated cellulose esters, and methods of making them |
| US20060100353A1 (en) * | 2004-11-08 | 2006-05-11 | Barsotti Robert J | Coating compositions for basecoats containing acrylic branched polymers |
| CA2612889C (en) | 2005-07-01 | 2011-06-28 | The Sherwin-Williams Company | Multi-layer coating system including a hydroxyl modified polyurethane dispersion binder |
| US20070028806A1 (en) * | 2005-08-03 | 2007-02-08 | Piro Bonnie D | Coating compositions having improved appearance containing coated titanium dioxide pigments |
| US20080085953A1 (en) * | 2006-06-05 | 2008-04-10 | Deepanjan Bhattacharya | Coating compositions comprising low molecular weight cellulose mixed esters and their use to improve anti-sag, leveling, and 20 degree gloss |
| WO2007145955A2 (en) | 2006-06-05 | 2007-12-21 | Eastman Chemical Company | Methods for improving the anti-sag, leveling, and gloss of coating compositions comprising low molecular weight cellulose mixed esters |
| US20070282038A1 (en) | 2006-06-05 | 2007-12-06 | Deepanjan Bhattacharya | Methods for improving the anti-sag, leveling, and gloss of coating compositions comprising low molecular weight cellulose mixed esters |
| TW200815508A (en) * | 2006-07-24 | 2008-04-01 | Fujifilm Corp | Cellulose acylate film, and polarizing plate and liquid crystal display device using the same |
| US20080090960A1 (en) * | 2006-09-18 | 2008-04-17 | Eastman Chemical Company | Low voc coating compositions comprising low molecular weight cellulose mixed esters and low molecular weight hydroxyl-containing polymers |
| US20080069963A1 (en) * | 2006-09-18 | 2008-03-20 | Eastman Chemical Company | Process for making low voc coating compositions comprising low molecular weight cellulose mixed esters and low molecular weight hydroxy-containing polymers |
-
2004
- 2004-03-09 US US10/796,235 patent/US7893138B2/en not_active Expired - Lifetime
- 2004-03-09 US US10/796,176 patent/US7585905B2/en not_active Expired - Lifetime
- 2004-03-11 JP JP2006507067A patent/JP2006520420A/ja active Pending
- 2004-03-11 JP JP2006507119A patent/JP2006523752A/ja not_active Withdrawn
- 2004-03-11 ES ES04719734T patent/ES2297399T3/es not_active Expired - Lifetime
- 2004-03-11 EP EP04719807.2A patent/EP1603952B1/en not_active Expired - Lifetime
- 2004-03-11 CN CNA2004800069143A patent/CN1761685A/zh active Pending
- 2004-03-11 WO PCT/US2004/007397 patent/WO2004083254A1/en not_active Ceased
- 2004-03-11 WO PCT/US2004/007573 patent/WO2004083253A1/en not_active Ceased
- 2004-03-11 CN CN2013100854159A patent/CN103145856A/zh active Pending
- 2004-03-11 CN CN2004800069675A patent/CN1820028B/zh not_active Expired - Lifetime
- 2004-03-11 PL PL04719734T patent/PL1603953T3/pl unknown
- 2004-03-11 EP EP20040719734 patent/EP1603953B1/en not_active Expired - Lifetime
- 2004-03-11 AT AT04719734T patent/ATE378357T1/de not_active IP Right Cessation
- 2004-03-11 DE DE200460010077 patent/DE602004010077T2/de not_active Expired - Lifetime
- 2004-03-11 EP EP10011755.5A patent/EP2301973B1/en not_active Expired - Lifetime
-
2009
- 2009-07-28 US US12/510,324 patent/US8003715B2/en not_active Expired - Lifetime
-
2011
- 2011-07-15 US US13/184,085 patent/US20110282049A1/en not_active Abandoned
- 2011-09-12 JP JP2011198648A patent/JP5588411B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE602004010077D1 (de) | 2007-12-27 |
| US8003715B2 (en) | 2011-08-23 |
| ATE378357T1 (de) | 2007-11-15 |
| WO2004083253A1 (en) | 2004-09-30 |
| CN1820028A (zh) | 2006-08-16 |
| DE602004010077T2 (de) | 2008-03-13 |
| EP1603952A1 (en) | 2005-12-14 |
| JP5588411B2 (ja) | 2014-09-10 |
| EP2301973A3 (en) | 2011-11-09 |
| US20090286095A1 (en) | 2009-11-19 |
| US7585905B2 (en) | 2009-09-08 |
| US7893138B2 (en) | 2011-02-22 |
| EP2301973A2 (en) | 2011-03-30 |
| CN1761685A (zh) | 2006-04-19 |
| EP1603953B1 (en) | 2007-11-14 |
| US20040180993A1 (en) | 2004-09-16 |
| CN103145856A (zh) | 2013-06-12 |
| EP2301973B1 (en) | 2013-10-30 |
| CN1820028B (zh) | 2011-04-06 |
| EP1603952B1 (en) | 2013-09-04 |
| EP1603953A1 (en) | 2005-12-14 |
| PL1603953T3 (pl) | 2008-06-30 |
| JP2006520420A (ja) | 2006-09-07 |
| JP2006523752A (ja) | 2006-10-19 |
| US20110282049A1 (en) | 2011-11-17 |
| US20040181009A1 (en) | 2004-09-16 |
| JP2012021163A (ja) | 2012-02-02 |
| WO2004083254A1 (en) | 2004-09-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2297399T3 (es) | Esteres de carboxialquilcelulosa de peso molecular bajo y su uso como aglomerantes de baja viscosidad y modificadores en composiciones de revestimiento. | |
| US7026470B2 (en) | Use of carboxymethyl cellulose acetate butyrate as a precoat or size for cellulosic man-made fiber boards | |
| JP5091116B2 (ja) | 低分子量セルロース混合エステル並びにそれらのコーティング組成物中の低粘度結合剤及び改質剤としての使用 | |
| US5994530A (en) | Carboxyalkyl cellulose esters for use in aqueous pigment dispersions | |
| AU722534B2 (en) | Carboxyalkyl cellulose esters | |
| EP2328983B1 (en) | Basecoat compositions comprising low molecular weight cellulose mixed esters | |
| US8124676B2 (en) | Basecoat coating compositions comprising low molecular weight cellulose mixed esters | |
| CA2755742A1 (en) | Refinish coating compositions comprising low molecular weight cellulose mixed esters | |
| MX2011009954A (es) | Composiciones de recubrimiento de reacabado que comprenden esteres mezclados de celulosa de bajo peso molecular. |