KR20010034843A - 전분 감성/그래프트 중합 조성물 및 그 제조방법과 용도 - Google Patents
전분 감성/그래프트 중합 조성물 및 그 제조방법과 용도 Download PDFInfo
- Publication number
- KR20010034843A KR20010034843A KR1020007012386A KR20007012386A KR20010034843A KR 20010034843 A KR20010034843 A KR 20010034843A KR 1020007012386 A KR1020007012386 A KR 1020007012386A KR 20007012386 A KR20007012386 A KR 20007012386A KR 20010034843 A KR20010034843 A KR 20010034843A
- Authority
- KR
- South Korea
- Prior art keywords
- starch
- weight
- solids
- composition
- polymer emulsion
- 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.)
- Granted
Links
- 229920002472 Starch Polymers 0.000 title claims abstract description 92
- 235000019698 starch Nutrition 0.000 title claims abstract description 92
- 239000008107 starch Substances 0.000 title claims abstract description 89
- 239000000203 mixture Substances 0.000 title claims description 48
- 238000000034 method Methods 0.000 title claims description 41
- 238000010559 graft polymerization reaction Methods 0.000 title description 3
- 230000015556 catabolic process Effects 0.000 title 1
- 238000006731 degradation reaction Methods 0.000 title 1
- 239000000178 monomer Substances 0.000 claims abstract description 50
- 239000000839 emulsion Substances 0.000 claims abstract description 46
- 229920000642 polymer Polymers 0.000 claims abstract description 45
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 34
- 229910052742 iron Inorganic materials 0.000 claims abstract description 17
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 14
- 230000035945 sensitivity Effects 0.000 claims abstract description 5
- 239000007787 solid Substances 0.000 claims description 47
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
- 238000000576 coating method Methods 0.000 claims description 23
- 239000004094 surface-active agent Substances 0.000 claims description 21
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 19
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 18
- 239000011248 coating agent Substances 0.000 claims description 18
- 239000000049 pigment Substances 0.000 claims description 16
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 12
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 12
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 9
- 229910052802 copper Inorganic materials 0.000 claims description 9
- 239000010949 copper Substances 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 9
- 229910052684 Cerium Inorganic materials 0.000 claims description 8
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 7
- 239000002736 nonionic surfactant Substances 0.000 claims description 7
- 125000000129 anionic group Chemical group 0.000 claims description 6
- 239000003945 anionic surfactant Substances 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 5
- 229910021529 ammonia Inorganic materials 0.000 claims description 5
- 238000007334 copolymerization reaction Methods 0.000 claims description 5
- 239000011343 solid material Substances 0.000 claims description 5
- 230000000087 stabilizing effect Effects 0.000 claims description 5
- 239000002562 thickening agent Substances 0.000 claims description 5
- 239000000080 wetting agent Substances 0.000 claims description 5
- 239000002518 antifoaming agent Substances 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims 2
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims 2
- 235000011511 Diospyros Nutrition 0.000 claims 1
- 244000236655 Diospyros kaki Species 0.000 claims 1
- WYCDUUBJSAUXFS-UHFFFAOYSA-N [Mn].[Ce] Chemical compound [Mn].[Ce] WYCDUUBJSAUXFS-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 5
- 206010070834 Sensitisation Diseases 0.000 abstract description 4
- 230000008313 sensitization Effects 0.000 abstract description 4
- 229910021645 metal ion Inorganic materials 0.000 abstract description 3
- 150000004965 peroxy acids Chemical class 0.000 abstract description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 24
- 239000000976 ink Substances 0.000 description 20
- 239000008367 deionised water Substances 0.000 description 17
- 229910021641 deionized water Inorganic materials 0.000 description 17
- 238000003756 stirring Methods 0.000 description 17
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 12
- 239000004908 Emulsion polymer Substances 0.000 description 10
- 239000000123 paper Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000004615 ingredient Substances 0.000 description 8
- 239000002585 base Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 6
- 239000012986 chain transfer agent Substances 0.000 description 5
- 238000007720 emulsion polymerization reaction Methods 0.000 description 5
- 229920000578 graft copolymer Polymers 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 4
- -1 antifoams Substances 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- XOCSLJFIGMLQLF-UHFFFAOYSA-N butyl 2-sulfanylpropanoate Chemical compound CCCCOC(=O)C(C)S XOCSLJFIGMLQLF-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000005002 finish coating Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002655 kraft paper Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 150000003440 styrenes Chemical class 0.000 description 3
- 125000000391 vinyl group Chemical class [H]C([*])=C([H])[H] 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- 229920005692 JONCRYL® Polymers 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- 239000004368 Modified starch Substances 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000012431 aqueous reaction media Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000008120 corn starch Substances 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 239000004815 dispersion polymer Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000019426 modified starch Nutrition 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 229920001567 vinyl ester resin Chemical class 0.000 description 2
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 1
- ICFXCSLDPCMWJI-UHFFFAOYSA-N 2,3-dimethylbut-2-enoic acid;2-ethyl-2-(hydroxymethyl)propane-1,3-diol Chemical compound CC(C)=C(C)C(O)=O.CCC(CO)(CO)CO ICFXCSLDPCMWJI-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- 229940095095 2-hydroxyethyl acrylate Drugs 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- RQAVKYPVSDCFJQ-UHFFFAOYSA-N 2-methyl-n-(2-methylpropoxy)prop-2-enamide Chemical compound CC(C)CONC(=O)C(C)=C RQAVKYPVSDCFJQ-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- ORDRGXFSRBRQQG-UHFFFAOYSA-N 6-methylheptyl 2-sulfanylpropanoate Chemical compound CC(C)CCCCCOC(=O)C(C)S ORDRGXFSRBRQQG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 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 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- MGFFVSDRCRVHLC-UHFFFAOYSA-N butyl 3-sulfanylpropanoate Chemical compound CCCCOC(=O)CCS MGFFVSDRCRVHLC-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- SRPCPRSDICCCRQ-UHFFFAOYSA-N chembl2004385 Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(N=NC3=C4C=CC=CC4=CC=C3O)=CC=C21 SRPCPRSDICCCRQ-UHFFFAOYSA-N 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- WFKDPJRCBCBQNT-UHFFFAOYSA-N n,2-dimethylprop-2-enamide Chemical compound CNC(=O)C(C)=C WFKDPJRCBCBQNT-UHFFFAOYSA-N 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- KCTMTGOHHMRJHZ-UHFFFAOYSA-N n-(2-methylpropoxymethyl)prop-2-enamide Chemical compound CC(C)COCNC(=O)C=C KCTMTGOHHMRJHZ-UHFFFAOYSA-N 0.000 description 1
- UTSYWKJYFPPRAP-UHFFFAOYSA-N n-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCNC(=O)C=C UTSYWKJYFPPRAP-UHFFFAOYSA-N 0.000 description 1
- DCBBWYIVFRLKCD-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-2-methylprop-2-enamide Chemical compound CN(C)CCNC(=O)C(C)=C DCBBWYIVFRLKCD-UHFFFAOYSA-N 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 239000002987 primer (paints) Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- 238000007342 radical addition reaction Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910052572 stoneware Inorganic materials 0.000 description 1
- SFXOHDOEOSCUCT-UHFFFAOYSA-N styrene;hydrochloride Chemical compound Cl.C=CC1=CC=CC=C1 SFXOHDOEOSCUCT-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
- C08L3/02—Starch; Degradation products thereof, e.g. dextrin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/106—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F251/00—Macromolecular compounds obtained by polymerising monomers on to polysaccharides or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/02—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to polysaccharides
-
- 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
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/02—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to polysaccharides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
- C08K2003/3045—Sulfates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Graft Or Block Polymers (AREA)
- Paints Or Removers (AREA)
- Polymerisation Methods In General (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
Description
성분 | 중량(그램) |
스티렌 | 162.5 |
n-부틸 아크릴레이트 | 162.5 |
n-부틸 메르캅토프로피오네이트 | 3.25 |
성분 | 중량(그램) |
스티렌 | 308.80 |
아크릴레이트 | 16.25 |
n-부틸 메르캅토프로피오네이트 | 3.25 |
성분 | 중량(그램) |
n-부틸 아크릴레이트 | 65.5 |
메틸 메타크릴레이트 | 65.5 |
스티렌 | 98.3 |
메타크릴산 | 98.3 |
n-부틸 메르캅토프로피오네이트 | 3.3 |
성분 | 설명 | 중량(g) |
카본 블랙 | Black Pearlsⓡ490(MA 블랙빌러리카에 소재하는 Cabot사 제품) | 50 |
그라인드 운반자 | 실시예3에서 제조된 중합체, 100%의 카르복실기가 수성 암모니아에 의해 중화됨,최종고체물질 15% | 83.3(고체물질 12.5g) |
물 | 수도물 | 115.4 |
소포제 | SurfynolⓡDF58(PA 알렌타운에 소재하는 Air사 제품) | 0.5 |
성분 | 설명 | 중량(g) |
베이스 그라인드 운반자 | 실시예4에서 제조된 분산액 | 80.0 |
저속 운반자 | 실시예3으로부터 제조된 중합체, 100%의 카르복실기가 수성 암모니아에의해 중화됨, 최종고체물질 15% | 12.1 |
물 | 수도물 | 7.9 |
샘플 | 종이색 | 핀홀 |
초벌/마무리 코팅 | 종이변색이 없음, 코팅제가 종이 섬유속으로 스며들지 않음 | 핀홀이 없음, 표면이 고르게 코팅됨 |
마무리 코팅제로 2회 코팅 | 변색됨, 코팅제가 종이 섬유속으로 스며듬 | 코팅에 의해 전체표면 유효범위보다 작은 핀홀이 생김, |
Claims (28)
- 전분 안정화 중합체 에멀젼을 제조하기에 적합한 조성물에 있어서,약 5 ~ 30중량%의 전분 고체물질, 약 1 ~ 5중량%의 과황산염 고체물질 및 적어도 약 70중량%의 에틸렌 불포화 모노머 고체물질을 함유하는 것을 특징으로 하는 조성물.
- 제 1 항에 있어서,약 0.5 ~ 1중량%의 계면활성제 모노머 고체물질을 추가로 함유하는 것을 특징으로 하는 조성물.
- 제 2 항에 있어서,상기 계면활성제는 음이온 및 비이온 계면활성제로 구성된 군 중에서 선택되는 것을 특징으로 하는 조성물.
- 제 1 항에 있어서,상기 조성물은 철, 니켈, 망간, 세륨 및 구리를 사실상 함유하지 않는 것을 특징으로 하는 조성물.
- 제 1 항에 있어서,상기 조성물은 철을 사실상 함유하지 않는 것을 특징으로 하는 조성물.
- 제 1 항에 있어서,상기 에틸렌 불포화 모노머는 아크릴산, 아크릴레이트, 메타크릴레이트 및 스티렌류로 구성된 군 중에서 선택되는 것을 특징으로 하는 조성물.
- 제 1 항에 있어서,상기 조성물은 또한 색소를 추가적으로 함유하는 것을 특징으로 하는 조성물.
- 전분 안정화 중합체 에멀젼을 제조하는 방법에 있어서,과황산염에 의해 제 1 항 기재의 전분이 감성되게 하는 단계와, 상기 전분의 적어도 일부가 제 1 항 기재의 과황산염에 의해 감성되는 동안, 이 감성되는 전분에 제 1 항 기재의 모노머를 가함으로써, 감성되는 전분이 상기 모노머와 그래프트 공중합되는 단계를 포함하는 것을 특징으로 하는 제조방법.
- 제 8 항에 있어서,첫번째 가해지는 모노머는 전분의 감성이 이루어지기 시작한 후 15분 보다 이르지 않게, 30분 보다 늦지 않게 가해지는 것을 특징으로 하는 제조방법.
- 제 8 항 기재의 제조방법에 의해 제조되는 전분 안정화 중합체 에멀젼.
- 제 8 항 기재의 제조방법에 의해 제조되는 에멀젼과 색소를 함유하는 코팅제.
- 제 1 항 기재의 조성물로부터 제조되는 전분 안정화 중합 에멀젼.
- 약 5 ~ 30중량%의 전분 고체물질, 약 1 ~ 5중량%의 과황산염 고체물질 및 적어도 약 70중량%의 에틸렌 불포화 모노머 고체물질을 함유하는 전분 안정화 중합체 에멀젼 약 10 ~ 90중량%와, 색소 고체물질 약 10 ~ 90중량%를 함유하는 것을 특징으로 하는 코팅제.
- 제 13 항에 있어서,상기 코팅제는 약 5 ~ 30중량%의 전분 고체물질, 약 1 ~ 5중량%의 과황산염 고체물질 및 적어도 약 70중량%의 에틸렌 불포화 모노머 고체물질을 함유하는 전분 안정화 중합체 에멀젼 약 10 ~ 20중량%와, 색소 고체물질 약 80 ~ 90중량%를 함유하는 것을 특징으로 하는 코팅제.
- 제 13 항에 있어서,상기 전분 안정화 중합체 에멀젼은 약 0.5 ~ 1중량%의 계면활성제 모노머 고체물질을 추가로 함유하는 것을 특징으로 하는 코팅제.
- 제 15 항에 있어서,상기 계면활성제는 음이온 및 비이온 계면활성제로 구성된 군 중에서 선택되는 것을 특징으로 하는 코팅제.
- 제 13 항에 있어서,상기 전분 안정화 중합체 에멀젼은 철, 니켈, 망간, 세륨 및 구리를 사실상 함유하지 않는 것을 특징으로 하는 코팅제.
- 제 13 항에 있어서,상기 전분 안정화 중합체 에멀젼은 철을 사실상 함유하지 않는 것을 특징으로 하는 코팅제.
- 제 13 항에 있어서,상기 에틸렌 불포화 모노머는 아크릴산, 아크릴레이트, 메타크릴레이트 및 스티렌류로 구성된 군 중에서 선택되는 것을 특징으로 하는 코팅제.
- 제 13 항에 있어서,상기 코팅제는 a)소포제, b)습윤제, c)증점제, d)베이스, e)암모니아 및 f)물로 구성된 군 중에서 선택되는 첨가제를 1종이상 함유하는 것을 특징으로 하는 코팅제.
- 약 5 ~ 30중량%의 전분 고체물질, 약 1 ~ 5중량%의 과황산염 고체물질 및 적어도 약 70중량%의 에틸렌 불포화 모노머 고체물질을 함유하는 전분 안정화 중합체 에멀젼 약 10 ~ 90중량%와, 색소 고체물질 약 10 ~ 90중량%를 함유하는 것을 특징으로 하는 잉크 조성물.
- 제 21 항에 있어서,상기 잉크 조성물은 약 5 ~ 30중량%의 전분 고체물질, 약 1 ~ 5중량%의 과황산염 고체물질 및 적어도 약 70중량%의 에틸렌 불포화 모노머 고체물질을 함유하는 전분 안정화 중합체 에멀젼 약 10 ~ 20중량%와, 색소 고체물질 약 80 ~ 90중량%를 함유하는 것을 특징으로 하는 잉크 조성물.
- 제 21 항에 있어서,상기 전분 안정화 중합체 에멀젼은 약 0.5 ~ 1중량%의 계면활성제 모노머 고체물질을 추가로 함유하는 것을 특징으로 하는 잉크 조성물.
- 제 23 항에 있어서,상기 계면활성제는 음이온 및 비이온 계면활성제로 구성된 군 중에서 선택되는 것을 특징으로 하는 잉크 조성물.
- 제 21 항에 있어서,상기 전분 안정화 중합체 에멀젼은 철, 니켈, 망간 세륨 및 구리를 사실상 함유하지 않는 것을 특징으로 하는 잉크 조성물.
- 제 21 항에 있어서,상기 전분 안정화 중합체 에멀젼은 철을 사실상 함유하지 않는 것을 특징으로 하는 잉크 조성물.
- 제 21 항에 있어서,상기 에틸렌 불포화 모노머는 아크릴산, 아크릴레이트, 메타크릴레이트 및 스티렌류로 구성된 군 중에서 선택되는 것을 특징으로 하는 잉크 조성물.
- 제 21 항에 있어서,상기 잉크 조성물은 a)소포제, b)습윤제, c)증점제, d)베이스, e)암모니아 및 f)물로 구성된 군 중에서 선택되는 첨가제를 1종이상 함유하는 것을 특징으로 하는 잉크 조성물.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/074,536 US6090884A (en) | 1998-05-07 | 1998-05-07 | Starch degradation/graft polymerization composition, process, and uses thereof |
US09/074,536 | 1998-05-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20010034843A true KR20010034843A (ko) | 2001-04-25 |
KR100719464B1 KR100719464B1 (ko) | 2007-05-18 |
Family
ID=22120087
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020007012386A Expired - Fee Related KR100719464B1 (ko) | 1998-05-07 | 1999-05-03 | 전분 감성/그래프트 중합 조성물 및 그 제조방법과 용도 |
Country Status (14)
Country | Link |
---|---|
US (1) | US6090884A (ko) |
EP (1) | EP1082370B1 (ko) |
JP (1) | JP4527878B2 (ko) |
KR (1) | KR100719464B1 (ko) |
CN (1) | CN1127528C (ko) |
AR (1) | AR016469A1 (ko) |
AT (1) | ATE272084T1 (ko) |
AU (1) | AU3781899A (ko) |
CA (1) | CA2331420C (ko) |
DE (1) | DE69918984T2 (ko) |
DK (1) | DK1082370T3 (ko) |
ES (1) | ES2226382T3 (ko) |
TW (1) | TW552298B (ko) |
WO (1) | WO1999057166A1 (ko) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6210475B1 (en) * | 1999-09-03 | 2001-04-03 | Bayer Corporation | Use of hydroxyalkylated starches for improved emulsification of sizing agents |
CA2532918C (en) * | 2003-07-25 | 2012-07-10 | Basf Aktiengesellschaft | Aqueous dispersions of hydrosoluble polymerisates of ethylenically unsaturated anionic monomers, method for the production and use thereof |
CN1326928C (zh) * | 2004-12-20 | 2007-07-18 | 陈明忠 | 淀粉类生物降解塑料母料及其制备方法 |
CN100344830C (zh) * | 2006-05-16 | 2007-10-24 | 上海迪纺纺织科技有限公司 | 冷转移印花纸用色素隔离剂 |
CN100453158C (zh) * | 2007-06-12 | 2009-01-21 | 陕西科技大学 | 一种淀粉基表面活性剂的制备方法 |
US8613834B2 (en) | 2008-04-03 | 2013-12-24 | Basf Se | Paper coating or binding formulations and methods of making and using same |
US9175179B2 (en) * | 2008-11-18 | 2015-11-03 | Sun Chemical Corporation | Printing ink and coating compositions containing derivatives of starch and modified starch |
KR101449795B1 (ko) * | 2012-02-27 | 2014-10-13 | (주)노루페인트 | 비닐온실용 도료 조성물 및 이를 사용한 도막의 형성방법 |
US9540473B2 (en) * | 2013-03-13 | 2017-01-10 | Akzo Nobel Chemicals International B.V. | Rheology modifiers |
CN105682749B (zh) * | 2013-11-13 | 2019-06-07 | 联合碳化化学品及塑料技术有限责任公司 | 碱可膨胀的交联丙烯酸酯共聚物,其制造方法,以及包含其的组合物 |
FR3024874B1 (fr) * | 2014-08-14 | 2016-09-02 | Roquette Freres | Copolymere de dextrine avec du styrene et un ester acrylique, son procede de fabrication et son utilisation pour le couchage papetier |
CN107011735A (zh) * | 2017-05-11 | 2017-08-04 | 黄山市古城歙砚有限公司 | 一种高细度的墨及其制备方法 |
JP7163646B2 (ja) * | 2018-07-11 | 2022-11-01 | 星光Pmc株式会社 | 水性印刷インキ用コアシェルエマルションの製造方法および水性印刷インキ用コアシェルエマルション |
US20220306791A1 (en) * | 2019-06-14 | 2022-09-29 | Basf Se | Aqueous polymer dispersions suitable as opacifiers in liquid formulations |
JP7472614B2 (ja) * | 2020-04-10 | 2024-04-23 | artience株式会社 | 水性フレキソインキおよび印刷物 |
US20240158556A1 (en) | 2021-04-16 | 2024-05-16 | Wacker Chemie Ag | Starch hybrid copolymers |
WO2024183924A1 (en) | 2023-03-09 | 2024-09-12 | Wacker Chemie Ag | Starch hybrid copolymers |
Family Cites Families (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3332897A (en) * | 1964-12-21 | 1967-07-25 | Nat Starch Chem Corp | Process of grafting monomers onto polysaccharides, and acylating product to obtain an ester |
US3640925A (en) * | 1969-10-16 | 1972-02-08 | Westvaco Corp | Process for the simultaneous gelatinization and graft copolymerization of monomers onto starch |
US3769248A (en) * | 1971-10-06 | 1973-10-30 | Anheuser Busch | Starch derivative protective colloids in emulsion polymer systems |
US4079025A (en) * | 1976-04-27 | 1978-03-14 | A. E. Staley Manufacturing Company | Copolymerized starch composition |
IL52434A (en) * | 1976-07-09 | 1980-06-30 | British Industrial Plastics | Manufacture of resin-containing oxidized starch solutions |
DE2659133C2 (de) * | 1976-12-28 | 1978-09-21 | Roehm Gmbh, 6100 Darmstadt | Verfahren zur Herstellung von blockfesten Überzügen |
US4131576A (en) * | 1977-12-15 | 1978-12-26 | National Starch And Chemical Corporation | Process for the preparation of graft copolymers of a water soluble monomer and polysaccharide employing a two-phase reaction system |
JPS55123610A (en) * | 1979-03-17 | 1980-09-24 | Nichiden Kagaku Kk | Modified starch and its preparation |
US4322322A (en) * | 1979-07-03 | 1982-03-30 | "Graanderivaten Raffinaderijen Amylum", In Het Kort: "G.R. Amylum", Vroeger Glucoseries Reunies Genoemd | Method for preparing a water-containing vinyl acetate polymer dispersion, dispersion thus prepared and protective colloid used thereby |
US4301017A (en) * | 1980-04-28 | 1981-11-17 | Standard Brands Incorporated | Stable, liquid starch graft copolymer composition |
DE3046490A1 (de) * | 1980-12-10 | 1982-07-15 | Hoechst Ag, 6000 Frankfurt | Solvatisierte salze von dinitrophenyl-cyanamiden, verfahren zu ihrer herstellung und ihre verwendung |
JPS59115375A (ja) * | 1982-12-22 | 1984-07-03 | Sugiyama Sangyo Kagaku Kenkyusho | ホルマリン系接着剤 |
DE3323851A1 (de) * | 1983-07-01 | 1985-01-03 | Wacker-Chemie GmbH, 8000 München | Verfahren zur herstellung waessriger polymerdispersionen und ihre verwendung |
DE3323804A1 (de) * | 1983-07-01 | 1985-01-03 | Wacker-Chemie GmbH, 8000 München | Verfahren zur herstellung waessriger polymerdispersionen und ihre verwendung |
US4684708A (en) * | 1985-03-11 | 1987-08-04 | Akzo N.V. | Cationic grafted starch copolymers |
CN1006551B (zh) * | 1985-05-13 | 1990-01-24 | 湖北省化学研究所 | 淀粉基超级吸水剂的制备 |
US4839450A (en) * | 1987-11-17 | 1989-06-13 | The United States Of America As Represented By The Secretary Of Agriculture | Moisture-shrinkable films from starch graft copolymers |
USH502H (en) * | 1987-12-21 | 1988-08-02 | The United States Of America As Represented By The Secretary Of The Army | High speed precision optical fiber winding system |
US5095054A (en) * | 1988-02-03 | 1992-03-10 | Warner-Lambert Company | Polymer compositions containing destructurized starch |
GB8806692D0 (en) * | 1988-03-21 | 1988-04-20 | Cerestar Holding Bv | Acrylate polymer compositions |
US5003022A (en) * | 1989-02-10 | 1991-03-26 | Penford Products Company | Starch graft polymers |
US5055541A (en) * | 1989-06-27 | 1991-10-08 | Sequa Chemicals, Inc. | Starch polymer graft composition and method of preparation |
US5026746A (en) * | 1989-06-26 | 1991-06-25 | Sequa Chemicals, Inc. | Starch based binder composition for non-woven fibers or fabrics |
US5116890A (en) * | 1989-06-26 | 1992-05-26 | Sequa Chemicals, Inc. | Non-formaldehyde self-crosslinking latex |
US5116927A (en) * | 1989-06-27 | 1992-05-26 | Sequa Chemicals, Inc. | Starch polymer graft composition and method of preparation |
US5082882A (en) * | 1989-11-30 | 1992-01-21 | Phillips Petroleum Company | Use of starch in the preparation of polymers |
DE4038732A1 (de) * | 1990-12-05 | 1992-06-11 | Henkel Kgaa | Mit synthetischen polymerverbindungen modifizierte werkstoffe und/oder formteile auf staerkebasis und verfahren zu ihrer herstellung |
TW207987B (ko) * | 1991-03-20 | 1993-06-21 | Hoechst Ag | |
JPH04301017A (ja) * | 1991-03-29 | 1992-10-23 | Nippon Steel Corp | 還元ガス供給ノズル構造 |
DE4133193A1 (de) * | 1991-10-07 | 1993-04-08 | Basf Ag | Waessrige polymerisatdispersionen |
ATE157133T1 (de) * | 1992-06-19 | 1997-09-15 | Penford Products Co | Bindemittel aus kationischer staerke/vinylacetat zum beschichten von pappe |
DE4338486A1 (de) * | 1993-11-11 | 1995-08-10 | Basf Ag | Verfahren zur Herstellung von Aufzeichnungsmaterialien für Tintenstrahldrucker |
US5525414A (en) * | 1994-02-03 | 1996-06-11 | Penford Products Co. | Method and materials for coating synthetic textile compositions |
US5523372A (en) * | 1994-06-29 | 1996-06-04 | Uni-Star Industries Ltd. | Starch graft copolymer from prime starch |
US5403875A (en) * | 1994-05-12 | 1995-04-04 | Rohm And Haas Company | Melt-processed polymer blends |
US5532300A (en) * | 1994-08-12 | 1996-07-02 | National Starch And Chemical Investment Holding Corporation | Water-borne, water redispersible, laminating adhesives for nonwoven applications |
JP3381811B2 (ja) * | 1994-08-24 | 2003-03-04 | 荒川化学工業株式会社 | 製紙用添加剤 |
DE19518620C2 (de) * | 1995-05-24 | 1998-04-09 | Degussa | Pfropfcopolymere auf Basis von Mono-, Oligo- und Polysacchariden, Verfahren zu ihrer Herstellung und ihre Verwendung |
US5753021A (en) * | 1996-07-24 | 1998-05-19 | Eastman Kodak Company | Pigmented ink jet inks containing modified polysaccharide resin |
JP3800370B2 (ja) * | 1996-10-22 | 2006-07-26 | 荒川化学工業株式会社 | 抄き合わせ紙用添加剤および抄き合わせ紙の製造方法 |
-
1998
- 1998-05-07 US US09/074,536 patent/US6090884A/en not_active Expired - Lifetime
-
1999
- 1999-05-03 WO PCT/US1999/009629 patent/WO1999057166A1/en not_active Application Discontinuation
- 1999-05-03 ES ES99920281T patent/ES2226382T3/es not_active Expired - Lifetime
- 1999-05-03 DE DE69918984T patent/DE69918984T2/de not_active Expired - Lifetime
- 1999-05-03 AT AT99920281T patent/ATE272084T1/de not_active IP Right Cessation
- 1999-05-03 CA CA002331420A patent/CA2331420C/en not_active Expired - Fee Related
- 1999-05-03 JP JP2000547133A patent/JP4527878B2/ja not_active Expired - Fee Related
- 1999-05-03 EP EP99920281A patent/EP1082370B1/en not_active Expired - Lifetime
- 1999-05-03 AU AU37818/99A patent/AU3781899A/en not_active Abandoned
- 1999-05-03 KR KR1020007012386A patent/KR100719464B1/ko not_active Expired - Fee Related
- 1999-05-03 CN CN99805888A patent/CN1127528C/zh not_active Expired - Fee Related
- 1999-05-03 DK DK99920281T patent/DK1082370T3/da active
- 1999-05-07 AR ARP990102155A patent/AR016469A1/es unknown
- 1999-05-26 TW TW088107379A patent/TW552298B/zh not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
WO1999057166A1 (en) | 1999-11-11 |
CA2331420A1 (en) | 1999-11-11 |
ES2226382T3 (es) | 2005-03-16 |
TW552298B (en) | 2003-09-11 |
CN1127528C (zh) | 2003-11-12 |
DE69918984T2 (de) | 2005-07-21 |
JP2002513824A (ja) | 2002-05-14 |
JP4527878B2 (ja) | 2010-08-18 |
KR100719464B1 (ko) | 2007-05-18 |
EP1082370B1 (en) | 2004-07-28 |
AU3781899A (en) | 1999-11-23 |
CA2331420C (en) | 2009-08-18 |
EP1082370A1 (en) | 2001-03-14 |
DK1082370T3 (da) | 2004-10-04 |
US6090884A (en) | 2000-07-18 |
ATE272084T1 (de) | 2004-08-15 |
AR016469A1 (es) | 2001-07-04 |
DE69918984D1 (de) | 2004-09-02 |
CN1299380A (zh) | 2001-06-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100719464B1 (ko) | 전분 감성/그래프트 중합 조성물 및 그 제조방법과 용도 | |
US4803252A (en) | Particles of crosslinked polymer prepared by emulsion polymerization in the absence of dispersion stabilizer | |
JPH10502948A (ja) | 水性分散液の製法 | |
US20110152452A1 (en) | Emulsion polymerization process, polymer dispersion and film-forming composition | |
WO2007031419A1 (en) | New rheology modifiers for modifying the rheological behaviour of coating compositions | |
JPH0224310A (ja) | 尿素基を含有し且つエチレン性不飽和単量体を基礎とする分散物重合体、その製造方法およびその用途 | |
US6849681B2 (en) | Carboxylic acid-modified vinylic polymeric compositions | |
US6020061A (en) | Emulsion polymerization using polymeric surfactants | |
EP0391343A2 (en) | Very fine-sized aqueous polymeric microemulsions | |
CA1339436C (en) | Non-aqueous dispersion for alkyd formulations and method of manufacture | |
EP1534761B1 (en) | Rosin-fatty acid vinylic polymer compositions | |
EP1401877B1 (en) | Process for obtaining aqueous polymer dispersions | |
WO2020130994A2 (en) | Polymodal and alkali soluble resin supported emulsion polymers | |
JP2004323759A (ja) | ブロック共重合体を含む水性液及びその製造方法 | |
JPS63258913A (ja) | 硬化性水性樹脂分散液 | |
US6967227B1 (en) | Carboxyester-modified vinylic polymeric compositions | |
JPS62179504A (ja) | 水性フレキソインキ用樹脂バインダ−の製造方法 | |
JPH0346507B2 (ko) | ||
EP1275703A2 (en) | Water resistant polymer composition for ink formulation | |
AU4447302A (en) | Emulsion polymerization using polymeric surfactants |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0105 | International application |
Patent event date: 20001106 Patent event code: PA01051R01D Comment text: International Patent Application |
|
PG1501 | Laying open of application | ||
A201 | Request for examination | ||
AMND | Amendment | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20040210 Comment text: Request for Examination of Application |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20051020 Patent event code: PE09021S01D |
|
AMND | Amendment | ||
E601 | Decision to refuse application | ||
PE0601 | Decision on rejection of patent |
Patent event date: 20060330 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20051020 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |
|
J201 | Request for trial against refusal decision | ||
PJ0201 | Trial against decision of rejection |
Patent event date: 20060703 Comment text: Request for Trial against Decision on Refusal Patent event code: PJ02012R01D Patent event date: 20060330 Comment text: Decision to Refuse Application Patent event code: PJ02011S01I Appeal kind category: Appeal against decision to decline refusal Decision date: 20070226 Appeal identifier: 2006101005702 Request date: 20060703 |
|
AMND | Amendment | ||
PB0901 | Examination by re-examination before a trial |
Comment text: Amendment to Specification, etc. Patent event date: 20060802 Patent event code: PB09011R02I Comment text: Request for Trial against Decision on Refusal Patent event date: 20060703 Patent event code: PB09011R01I Comment text: Amendment to Specification, etc. Patent event date: 20051206 Patent event code: PB09011R02I Comment text: Amendment to Specification, etc. Patent event date: 20040210 Patent event code: PB09011R02I |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20060831 Patent event code: PE09021S01D |
|
B701 | Decision to grant | ||
PB0701 | Decision of registration after re-examination before a trial |
Patent event date: 20070226 Comment text: Decision to Grant Registration Patent event code: PB07012S01D Patent event date: 20060817 Comment text: Transfer of Trial File for Re-examination before a Trial Patent event code: PB07011S01I |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20070511 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20070514 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
PR1001 | Payment of annual fee |
Payment date: 20100511 Start annual number: 4 End annual number: 4 |
|
PR1001 | Payment of annual fee |
Payment date: 20110511 Start annual number: 5 End annual number: 5 |
|
PR1001 | Payment of annual fee |
Payment date: 20120507 Start annual number: 6 End annual number: 6 |
|
FPAY | Annual fee payment |
Payment date: 20130429 Year of fee payment: 7 |
|
PR1001 | Payment of annual fee |
Payment date: 20130429 Start annual number: 7 End annual number: 7 |
|
FPAY | Annual fee payment |
Payment date: 20140428 Year of fee payment: 8 |
|
PR1001 | Payment of annual fee |
Payment date: 20140428 Start annual number: 8 End annual number: 8 |
|
FPAY | Annual fee payment |
Payment date: 20150424 Year of fee payment: 9 |
|
PR1001 | Payment of annual fee |
Payment date: 20150424 Start annual number: 9 End annual number: 9 |
|
FPAY | Annual fee payment |
Payment date: 20160429 Year of fee payment: 10 |
|
PR1001 | Payment of annual fee |
Payment date: 20160429 Start annual number: 10 End annual number: 10 |
|
FPAY | Annual fee payment |
Payment date: 20170427 Year of fee payment: 11 |
|
PR1001 | Payment of annual fee |
Payment date: 20170427 Start annual number: 11 End annual number: 11 |
|
LAPS | Lapse due to unpaid annual fee | ||
PC1903 | Unpaid annual fee |
Termination category: Default of registration fee Termination date: 20190222 |