NO772912L - Interpolymer. - Google Patents

Interpolymer.

Info

Publication number: NO772912L
Authority: NO; Norway
Prior art keywords: weight; interpolymer; methacrylate; stated; acid
Prior art date: 1977-04-04

Application number

NO772912A

Other languages

English (en)

Norwegian (no)

Inventor

Ira John Westerman

Original Assignee

Goodrich Co B F

Priority date (The priority date 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 date listed.)

1977-04-04

Filing date

1977-08-22

Publication date

1978-10-05

1977-08-22 Application filed by Goodrich Co B F filed Critical Goodrich Co B F

1978-10-05 Publication of NO772912L publication Critical patent/NO772912L/no

Links

229920000642 polymer Polymers 0.000 claims description 56
239000000178 monomer Substances 0.000 claims description 40
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 28
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 22
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 19
-1 acrylic ester Chemical class 0.000 claims description 18
GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 claims description 18
125000004432 carbon atom Chemical group C* 0.000 claims description 12
239000002253 acid Substances 0.000 claims description 11
238000004132 cross linking Methods 0.000 claims description 10
RFIMISVNSAUMBU-UHFFFAOYSA-N 2-(hydroxymethyl)-2-(prop-2-enoxymethyl)propane-1,3-diol Chemical group OCC(CO)(CO)COCC=C RFIMISVNSAUMBU-UHFFFAOYSA-N 0.000 claims description 8
HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 claims description 8
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 7
COCLLEMEIJQBAG-UHFFFAOYSA-N 8-methylnonyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C(C)=C COCLLEMEIJQBAG-UHFFFAOYSA-N 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
239000003431 cross linking reagent Substances 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
229920000570 polyether Polymers 0.000 claims description 5
229910052700 potassium Inorganic materials 0.000 claims description 5
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
150000005846 sugar alcohols Polymers 0.000 claims description 4
239000004721 Polyphenylene oxide Substances 0.000 claims description 3
125000003342 alkenyl group Chemical group 0.000 claims description 3
229940086737 allyl sucrose Drugs 0.000 claims description 3
125000001033 ether group Chemical group 0.000 claims description 3
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
229910052744 lithium Inorganic materials 0.000 claims description 3
229910052708 sodium Inorganic materials 0.000 claims description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
150000008064 anhydrides Chemical class 0.000 claims description 2
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims description 2
LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
150000002500 ions Chemical class 0.000 claims description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
239000011976 maleic acid Substances 0.000 claims description 2
229940065472 octyl acrylate Drugs 0.000 claims description 2
ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 claims description 2
BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 claims description 2
WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 claims 1
125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
229910017464 nitrogen compound Inorganic materials 0.000 claims 1
150000002830 nitrogen compounds Chemical group 0.000 claims 1
229920001577 copolymer Polymers 0.000 description 30
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
238000010521 absorption reaction Methods 0.000 description 14
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 13
239000007788 liquid Substances 0.000 description 12
239000000463 material Substances 0.000 description 11
238000006116 polymerization reaction Methods 0.000 description 9
239000002904 solvent Substances 0.000 description 9
239000010408 film Substances 0.000 description 8
125000000217 alkyl group Chemical group 0.000 description 7
230000000694 effects Effects 0.000 description 6
210000002700 urine Anatomy 0.000 description 6
239000002250 absorbent Substances 0.000 description 5
230000002745 absorbent Effects 0.000 description 5
239000003054 catalyst Substances 0.000 description 5
239000000203 mixture Substances 0.000 description 5
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
239000007789 gas Substances 0.000 description 4
JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 4
KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Substances [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
239000003513 alkali Substances 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
150000001768 cations Chemical class 0.000 description 3
238000007334 copolymerization reaction Methods 0.000 description 3
239000012153 distilled water Substances 0.000 description 3
239000011953 free-radical catalyst Substances 0.000 description 3
238000007654 immersion Methods 0.000 description 3
239000002608 ionic liquid Substances 0.000 description 3
230000014759 maintenance of location Effects 0.000 description 3
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
150000002734 metacrylic acid derivatives Chemical class 0.000 description 3
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 3
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
239000011591 potassium Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 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
YACLCMMBHTUQON-UHFFFAOYSA-N 1-chloro-1-fluoroethane Chemical compound CC(F)Cl YACLCMMBHTUQON-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 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
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
150000008065 acid anhydrides Chemical class 0.000 description 2
150000001252 acrylic acid derivatives Chemical class 0.000 description 2
125000005250 alkyl acrylate group Chemical group 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000002585 base Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
229920006037 cross link polymer Polymers 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
239000000835 fiber Substances 0.000 description 2
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
125000005397 methacrylic acid ester group Chemical group 0.000 description 2
238000000034 method Methods 0.000 description 2
238000006386 neutralization reaction Methods 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000011734 sodium Substances 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
230000008719 thickening Effects 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
FEIQOMCWGDNMHM-KBXRYBNXSA-N (2e,4e)-5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)\C=C\C=C\C1=CC=CC=C1 FEIQOMCWGDNMHM-KBXRYBNXSA-N 0.000 description 1
XVOUMQNXTGKGMA-OWOJBTEDSA-N (E)-glutaconic acid Chemical compound OC(=O)C\C=C\C(O)=O XVOUMQNXTGKGMA-OWOJBTEDSA-N 0.000 description 1
239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
UGCSPKPEHQEOSR-UHFFFAOYSA-N 1,1,2,2-tetrachloro-1,2-difluoroethane Chemical compound FC(Cl)(Cl)C(F)(Cl)Cl UGCSPKPEHQEOSR-UHFFFAOYSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
RFCAUADVODFSLZ-UHFFFAOYSA-N 1-Chloro-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)Cl RFCAUADVODFSLZ-UHFFFAOYSA-N 0.000 description 1
HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
ZVHZPFSWZWSDEN-UHFFFAOYSA-N 1-bromo-1-fluoroethane Chemical compound CC(F)Br ZVHZPFSWZWSDEN-UHFFFAOYSA-N 0.000 description 1
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
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
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical compound OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 description 1
IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical compound OC(=O)C(=C)C#N IJVRPNIWWODHHA-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
CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
ONPJWQSDZCGSQM-UHFFFAOYSA-N 2-phenylprop-2-enoic acid Chemical compound OC(=O)C(=C)C1=CC=CC=C1 ONPJWQSDZCGSQM-UHFFFAOYSA-N 0.000 description 1
KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 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
CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 1
XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
GXLIFJYFGMHYDY-ZZXKWVIFSA-N 4-chlorocinnamic acid Chemical compound OC(=O)\C=C\C1=CC=C(Cl)C=C1 GXLIFJYFGMHYDY-ZZXKWVIFSA-N 0.000 description 1
JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
239000004338 Dichlorodifluoromethane Substances 0.000 description 1
OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
229920001131 Pulp (paper) Polymers 0.000 description 1
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
239000011358 absorbing material Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
229940091181 aconitic acid Drugs 0.000 description 1
150000003926 acrylamides Chemical class 0.000 description 1
150000001253 acrylic acids Chemical class 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 1
239000004411 aluminium Substances 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
150000005840 aryl radicals Chemical class 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
XNNQFQFUQLJSQT-UHFFFAOYSA-N bromo(trichloro)methane Chemical compound ClC(Cl)(Cl)Br XNNQFQFUQLJSQT-UHFFFAOYSA-N 0.000 description 1
RJCQBQGAPKAMLL-UHFFFAOYSA-N bromotrifluoromethane Chemical compound FC(F)(F)Br RJCQBQGAPKAMLL-UHFFFAOYSA-N 0.000 description 1
238000012662 bulk polymerization Methods 0.000 description 1
RLYNGYDVXRKEOO-SQQVDAMQSA-N but-2-enoic acid;(e)-but-2-enoic acid Chemical compound CC=CC(O)=O.C\C=C\C(O)=O RLYNGYDVXRKEOO-SQQVDAMQSA-N 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
229950005499 carbon tetrachloride Drugs 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
150000001767 cationic compounds Chemical group 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
235000019406 chloropentafluoroethane Nutrition 0.000 description 1
AFYPFACVUDMOHA-UHFFFAOYSA-N chlorotrifluoromethane Chemical compound FC(F)(F)Cl AFYPFACVUDMOHA-UHFFFAOYSA-N 0.000 description 1
229930016911 cinnamic acid Natural products 0.000 description 1
235000013985 cinnamic acid Nutrition 0.000 description 1
GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
229940018557 citraconic acid Drugs 0.000 description 1
MRIZMKJLUDDMHF-UHFFFAOYSA-N cumene;hydrogen peroxide Chemical class OO.CC(C)C1=CC=CC=C1 MRIZMKJLUDDMHF-UHFFFAOYSA-N 0.000 description 1
125000004966 cyanoalkyl group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
GTBGXKPAKVYEKJ-UHFFFAOYSA-N decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(C)=C GTBGXKPAKVYEKJ-UHFFFAOYSA-N 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 description 1
125000004386 diacrylate group Chemical group 0.000 description 1
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
KHAYCTOSKLIHEP-UHFFFAOYSA-N docosyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=C KHAYCTOSKLIHEP-UHFFFAOYSA-N 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229960003750 ethyl chloride Drugs 0.000 description 1
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
239000012530 fluid Substances 0.000 description 1
UHCBBWUQDAVSMS-UHFFFAOYSA-N fluoroethane Chemical compound CCF UHCBBWUQDAVSMS-UHFFFAOYSA-N 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
229910001385 heavy metal Inorganic materials 0.000 description 1
SCFQUKBBGYTJNC-UHFFFAOYSA-N heptyl prop-2-enoate Chemical compound CCCCCCCOC(=O)C=C SCFQUKBBGYTJNC-UHFFFAOYSA-N 0.000 description 1
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-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
239000003701 inert diluent Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229940102253 isopropanolamine Drugs 0.000 description 1
PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
WMFOQBRAJBCJND-UHFFFAOYSA-M lithium hydroxide Substances [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
230000002175 menstrual effect Effects 0.000 description 1
HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
125000005395 methacrylic acid group Chemical class 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 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
HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
FEZFGASTIQVZSC-UHFFFAOYSA-N nonanoyl nonaneperoxoate Chemical compound CCCCCCCCC(=O)OOC(=O)CCCCCCCC FEZFGASTIQVZSC-UHFFFAOYSA-N 0.000 description 1
MDYPDLBFDATSCF-UHFFFAOYSA-N nonyl prop-2-enoate Chemical compound CCCCCCCCCOC(=O)C=C MDYPDLBFDATSCF-UHFFFAOYSA-N 0.000 description 1
NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000010422 painting Methods 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
229910001414 potassium ion Inorganic materials 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Substances [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 1
229910001415 sodium ion Inorganic materials 0.000 description 1
229940045872 sodium percarbonate Drugs 0.000 description 1
SPDUKHLMYVCLOA-UHFFFAOYSA-M sodium;ethaneperoxoate Chemical compound [Na+].CC(=O)O[O-] SPDUKHLMYVCLOA-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
UFHILTCGAOPTOV-UHFFFAOYSA-N tetrakis(ethenyl)silane Chemical compound C=C[Si](C=C)(C=C)C=C UFHILTCGAOPTOV-UHFFFAOYSA-N 0.000 description 1
XJPKDRJZNZMJQM-UHFFFAOYSA-N tetrakis(prop-2-enyl)stannane Chemical compound C=CC[Sn](CC=C)(CC=C)CC=C XJPKDRJZNZMJQM-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000010409 thin film Substances 0.000 description 1
UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
229940029284 trichlorofluoromethane Drugs 0.000 description 1
229940096522 trimethylolpropane triacrylate Drugs 0.000 description 1
239000008096 xylene Substances 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/93—Water swellable or hydrophilic
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/932—Thickener or dispersant for aqueous system

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Absorbent Articles And Supports Therefor (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)

NO772912A 1977-04-04 1977-08-22 Interpolymer. NO772912L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/784,099 US4062817A (en)	1977-04-04	1977-04-04	Water absorbent polymers comprising unsaturated carboxylic acid, acrylic ester containing alkyl group 10-30 carbon atoms, and another acrylic ester containing alkyl group 2-8 carbon atoms

Publications (1)

Publication Number	Publication Date
NO772912L true NO772912L (no)	1978-10-05

Family

ID=25131342

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO772912A NO772912L (no)	1977-04-04	1977-08-22	Interpolymer.

Country Status (15)

Country	Link
US (1)	US4062817A (fr)
JP (1)	JPS53123490A (fr)
AU (1)	AU510453B2 (fr)
BE (1)	BE858800A (fr)
CA (1)	CA1086447A (fr)
CH (1)	CH636363A5 (fr)
DE (1)	DE2734298A1 (fr)
DK (1)	DK337777A (fr)
FR (1)	FR2386565A1 (fr)
GB (1)	GB1589975A (fr)
IT (1)	IT1085352B (fr)
MX (1)	MX145592A (fr)
NL (1)	NL189674C (fr)
NO (1)	NO772912L (fr)
SE (1)	SE425974B (fr)

Families Citing this family (183)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4167464A (en) *	1978-10-16	1979-09-11	The B. F. Goodrich Company	Photopolymerized hydrophilic interpolymers of unsaturated carboxylic acid and esters
US4267103A (en) *	1978-12-07	1981-05-12	The B. F. Goodrich Company	Solvent polymerization of carboxyl containing monomers
JPS55164209A (en) *	1979-06-11	1980-12-20	Nippon Carbide Ind Co Ltd	Thermoplastic resin lubricant and lubricating thermoplastic resin composition
US4401795A (en) *	1979-07-11	1983-08-30	Nl Industries Inc.	Polymeric polyelectrolytes
JPS56501091A (fr) *	1979-09-11	1981-08-06
US4270977A (en) *	1979-11-01	1981-06-02	Nl Industries, Inc.	Process for preparing water sorptive products
BR8009002A (pt) *	1979-12-26	1981-10-20	Goodrich Co B F	Interpolimeros hidrofilos fotopolimerizados de acidos acrilico e agentes de reticulacao polifuncionais
JPS5691838A (en) *	1979-12-27	1981-07-25	Nippon Kayaku Co Ltd	Water absorbing material
DE3002287A1 (de) *	1980-01-23	1981-07-30	Agfa-Gevaert Ag, 5090 Leverkusen	Mehrwertige metallkationen enthaltende anionische mischpolymerisate und ihre verwendung in fotografischen materialien
WO1982000147A1 (fr) *	1980-07-08	1982-01-21	Co B F Goodrich	Interpolymeres hydrophiles d'acides acryliques et d'un acrylate
US4486489A (en) *	1980-07-08	1984-12-04	The B. F. Goodrich Company	Films of hydrophilic interpolymers of neutralized acrylic acid, hydroxyalkyl methacrylate or dialkylaminoalkyl (meth)acrylate and optionally a cross-linking agent
AU7328581A (en) *	1981-03-16	1982-10-06	Hwa, S.C.P.	Novel protein curd product and process of preparation
US4375533A (en) *	1981-07-08	1983-03-01	The Bf Goodrich Company	Polymerization process for carboxyl containing polymers
US4755562A (en) *	1986-06-10	1988-07-05	American Colloid Company	Surface treated absorbent polymers
US4552938A (en) *	1981-10-26	1985-11-12	American Colloid Company	Process for preparing dry solid water absorbing polyacrylate resin
US4985518A (en) *	1981-10-26	1991-01-15	American Colloid Company	Process for preparing water-absorbing resins
US4419502A (en) *	1982-09-29	1983-12-06	The B. F. Goodrich Company	Polymerization process for carboxyl containing polymers
US4610678A (en) *	1983-06-24	1986-09-09	Weisman Paul T	High-density absorbent structures
DE3335954A1 (de) *	1983-10-04	1985-04-04	Roland Dipl.-Kaufm. 7022 Leinfelden-Echterdingen Belz	Verfahren zur durchfuehrung von chemischen reaktionen, insbesondere zur herstellung von kunststoffen mit hilfe von extrudern und anlage hierzu
US4535098A (en) *	1984-03-12	1985-08-13	The Dow Chemical Company	Material for absorbing aqueous fluids
JPH0633006B2 (ja) *	1984-03-20	1994-05-02	大日本印刷株式会社	感熱転写シート
EP0264368B1 (fr) *	1984-04-05	1991-05-15	The Dow Chemical Company	Procede de preparation de resines ameliorees faiblement acides et de resines poreuses faiblement acides
US4614751A (en) *	1984-04-05	1986-09-30	The Dow Chemical Company	Process for preparing improved weak acid resins and porous weak acid resins
DE3682088D1 (de) *	1985-03-18	1991-11-28	Mitsubishi Petrochemical Co	Verfahren zur herstellung von wasserabsorbierenden polymeren.
US4654039A (en) *	1985-06-18	1987-03-31	The Proctor & Gamble Company	Hydrogel-forming polymer compositions for use in absorbent structures
USRE32649E (en) *	1985-06-18	1988-04-19	The Procter & Gamble Company	Hydrogel-forming polymer compositions for use in absorbent structures
US4764447A (en) *	1985-07-17	1988-08-16	Ricoh Co., Ltd.	Non-aqueous type resin dispersion and electrophotographic developer containing said resin
JPS62501568A (ja) *	1985-08-09	1987-06-25	ザ　ダウ　ケミカル　カンパニ−	水性流体の吸収のための材料
US4813945A (en) *	1986-02-26	1989-03-21	Arco Chemical Technology, Inc.	Ultrahigh water-absorbing fiber forming composition
US4892533A (en) *	1986-02-26	1990-01-09	Arco Chemical Technology, Inc.	Ultrahigh water-absorbing fiber-forming composition
CA1326416C (fr) *	1986-08-25	1994-01-25	Ralph Xavier Ewall	Pansements de polymere
DE3631814A1 (de) *	1986-09-19	1988-03-31	Basf Ag	Geringfuegig vernetzte, wasserloesliche polymaleinsaeure, verfahren zu deren herstellung und verwendung
KR880005918A (ko) *	1986-11-10	1988-07-21	원본미기재	안정하며 빨리 분해되는 국소피부조성물
US4735843A (en) *	1986-12-18	1988-04-05	The Procter & Gamble Company	Selectively surface-hydrophilic porous or perforated sheets
US4758641A (en) *	1987-02-24	1988-07-19	The B F Goodrich Company	Polycarboxylic acids with small amount of residual monomer
FR2623516B1 (fr) *	1987-11-19	1994-04-15	Saint Gobain Vitrage	Composition pour revetement antibuee, produit revetu de cette composition et procede de preparation de ce produit
US4996274A (en) *	1988-02-19	1991-02-26	The B. F. Goodrich Company	Polycarboxylic acids with higher thickening capacity and better clarity
DE3813651A1 (de) *	1988-04-22	1989-11-02	Henkel Kgaa	Verdickungsmittel auf basis waessriger emulsions-copolymerlatices und ihre verwendung zur eindickung waessriger fluessigphasen
US4921904A (en) *	1988-12-19	1990-05-01	Nalco Chemical Company	Superabsorbent polymers
US5034139A (en) *	1989-06-19	1991-07-23	Nalco Chemical Company	Polymer composition comprising phosphorous-containing gelling agent and process thereof
US5149335A (en) *	1990-02-23	1992-09-22	Kimberly-Clark Corporation	Absorbent structure
DE4039899A1 (de) *	1990-12-14	1992-06-17	Henkel Kgaa	Lyo-gel, seine herstellung und verwendung zum dichten
US6482373B1 (en)	1991-04-12	2002-11-19	Newmont Usa Limited	Process for treating ore having recoverable metal values including arsenic containing components
GB9114095D0 (en)	1991-06-29	1991-08-14	Allstate Limited	Improvements in water-soluble polymers
US5332559A (en) *	1991-07-10	1994-07-26	Newmont Gold Co.	Biooxidation process for recovery of metal values from sulphur-containing ore materials
US6696283B1 (en)	1991-07-10	2004-02-24	Newmont Usa Limited	Particulate of sulfur-containing ore materials and heap made therefrom
US6383458B1 (en)	1991-07-10	2002-05-07	Newmont Mining Corporation	Biooxidation process for recovery of metal values from sulfur-containing ore materials
TW213474B (fr) *	1991-07-17	1993-09-21	Cargill Inc
JP3148307B2 (ja) *	1991-11-07	2001-03-19	ライオン株式会社	塩感応性ポリマー
CA2114815C (fr)	1993-02-24	2005-06-14	Mark Kevin Melius	Composite absorbant
US5393608A (en) *	1993-05-25	1995-02-28	Moore Business Forms	Non-silicone release polymer
DE69527704T2 (de) *	1994-02-17	2002-12-05	The Procter & Gamble Company, Cincinnati	Poröses absorbierendes material mit modifierter oberflächen-charakteristik und verfahren zu seiner herstellung
US5843575A (en) *	1994-02-17	1998-12-01	The Procter & Gamble Company	Absorbent members comprising absorbent material having improved absorbent property
US5849405A (en) *	1994-08-31	1998-12-15	The Procter & Gamble Company	Absorbent materials having improved absorbent property and methods for making the same
US5422233A (en) *	1994-05-17	1995-06-06	Polaroid Corporation	Photographic processing compositions including hydrophobically modified thickening agent
US5425939A (en) *	1994-05-27	1995-06-20	Elizabeth Arden Company, Division Of Conopco, Inc.	Thickened cosmetic compositions
DE4426008A1 (de)	1994-07-22	1996-01-25	Cassella Ag	Hydrophile, hochquellfähige Hydrogele
EP0708119A1 (fr)	1994-10-21	1996-04-24	Air Products And Chemicals, Inc.	Compositions aqueuses de polymères absorbant de l'eau auto-réticulants
US5719201A (en) *	1995-03-30	1998-02-17	Woodbridge Foam Corporation	Superabsorbent hydrophilic isocyanate-based foam and process for production thereof
US5674917A (en) *	1995-03-30	1997-10-07	Woodbridge Foam Corporation	Superabsorbent hydrophilic isocyanate-based foam and process for production thereof
DE19601763A1 (de) *	1996-01-19	1997-07-24	Hoechst Ag	Verwendung von Tensiden bei der Trocknung von hydrophilen, hochquellfähigen Hydrogelen
DE19601764A1 (de)	1996-01-19	1997-07-24	Hoechst Ag	Verfahren zur Herstellung hydrophiler, hochquellfähiger Hydrogele
US6730387B2 (en)	1996-04-24	2004-05-04	The Procter & Gamble Company	Absorbent materials having improved structural stability in dry and wet states and making methods therefor
US5744509A (en) *	1996-07-01	1998-04-28	Woodbridge Foam Corporation	Foamed polymer and process for production thereof
US5624971A (en) *	1996-07-01	1997-04-29	Woodbridge Foam Corporation	Foamed polymer and process for production thereof
US5817703A (en) *	1996-09-30	1998-10-06	Woodbridge Foam Corporation	Rebond foam and process for production thereof
US7291137B2 (en)	1997-03-27	2007-11-06	The Procter & Gamble Company	Disposable absorbent articles having multiple absorbent core components including replaceable components
US6989005B1 (en)	1997-03-27	2006-01-24	The Procter & Gamble Company	Absorbent articles having removable components
US7601145B2 (en)	1997-03-27	2009-10-13	The Procter & Gamble Company	Disposable absorbent articles having multiple absorbent core components including replaceable components
US6932800B2 (en)	1997-03-27	2005-08-23	The Procter & Gamble Company	Absorbent articles comprising a material having a high vertical wicking capacity
US7670324B2 (en)	1997-03-27	2010-03-02	The Procter And Gamble Company	Disposable absorbent articles with replaceable absorbent core components having regions of permeability and impermeability on same surface
US5856410A (en) *	1997-05-23	1999-01-05	Amcol International Corporation	Polyacrylate superabsorbent post-polymerization neutralized with solid, non-hydroxyl neutralizing agent.
DE69811293T2 (de) *	1997-06-20	2003-10-23	Rohm And Haas Co., Philadelphia	Polymerzusammensetzungen
HUP0102559A3 (en)	1998-03-13	2001-12-28	Procter & Gamble	Absorbent structures comprising fluid storage members with improved ability to dewater distribution members
US6713661B1 (en)	1998-04-28	2004-03-30	The Procter & Gamble Company	Absorbent articles providing improved fit when wet
US6534572B1 (en)	1998-05-07	2003-03-18	H. B. Fuller Licensing & Financing, Inc.	Compositions comprising a thermoplastic component and superabsorbent polymer
DE19849499A1 (de)	1998-10-27	2000-05-04	Basf Ag	Verfahren zur vollständigen Trocknung von Hydrogelen
DE19854573A1 (de)	1998-11-26	2000-05-31	Basf Ag	Verfahren zur Nachvernetzung von Hydrogelen mit 2-Oxo-tetrahydro-1,3-oxazinen
GB9903140D0 (en)	1999-02-12	1999-04-07	Basf Ag	Interpolymers
US6297337B1 (en)	1999-05-19	2001-10-02	Pmd Holdings Corp.	Bioadhesive polymer compositions
US6521431B1 (en)	1999-06-22	2003-02-18	Access Pharmaceuticals, Inc.	Biodegradable cross-linkers having a polyacid connected to reactive groups for cross-linking polymer filaments
US6610900B1 (en)	1999-08-27	2003-08-26	Kimberly-Clark Worldwide, Inc.	Absorbent article having superabsorbent in discrete pockets on a stretchable substrate
US6429350B1 (en)	1999-08-27	2002-08-06	Kimberly-Clark Worldwide, Inc.	Absorbent article having superabsorbent pockets in a non-absorbent carrier layer
JP3908535B2 (ja)	1999-09-27	2007-04-25	ザプロクターアンドギャンブルカンパニー	硬い表面のクリーニング組成物、予め湿らせた拭取り具、使用方法、及び前記組成物又は拭取り具及びすすぎをしないような強制的条件下において外観及び／又は衛生を改良し、クリーニング及びメンテナンスを容易にするための使用説明書を含有する物品。
US6433061B1 (en)	2000-10-24	2002-08-13	Noveon Ip Holdings Corp.	Rheology modifying copolymer composition
US7414017B2 (en)	2000-12-14	2008-08-19	The Clorox Company	Low residue cleaning solution comprising a C8-C10 alkylpolyglucoside
US7727211B2 (en) *	2001-07-23	2010-06-01	The Procter & Gamble Company	Absorbent article having a replaceable absorbent core component having an insertion pocket
US7476697B2 (en) *	2001-09-10	2009-01-13	Patacca Thomas R	Tooth coating composition
US7189888B2 (en)	2001-12-21	2007-03-13	Kimberly-Clark Worldwide, Inc.	Nonabsorbent surge layer having discrete regions of superabsorbent and method for making
JP3963750B2 (ja) *	2002-03-25	2007-08-22	日本電産サンキョー株式会社	曲面切削加工方法
DE10225943A1 (de)	2002-06-11	2004-01-08	Basf Ag	Verfahren zur Herstellung von Estern von Polyalkoholen
NL1023720C2 (nl) *	2003-06-23	2004-12-28	Univ Eindhoven Tech	Werkwijze voor het wijzigen van de transporteigenschappen van een materiaal, werkwijze voor het vrijmaken van een werkstof uit een implantaat, evenals implantaat met werkstof.
ATE492301T1 (de)	2003-06-30	2011-01-15	Procter & Gamble	Absorbierende artikel enthaltend beschichtete superabsorbierende partikel
US7311968B2 (en) *	2004-06-30	2007-12-25	The Procter & Gamble Company	Absorbent structures comprising coated super-absorbent polymer particles
EP1504772A1 (fr) *	2003-08-06	2005-02-09	The Procter & Gamble Company	Polymères superabsorbants contenant des agents de réticulation de surface activables par rayonnement et leur procédé de fabrication
MXPA06001295A (es) *	2003-08-06	2006-04-11	Procter & Gamble	Articulo absorbente que comprende material recubierto hinchable en agua.
MXPA06001296A (es) *	2003-08-06	2006-04-11	Procter & Gamble	Procedimiento para producir material gelificante absorbente tratado superficialmente.
ATE495764T1 (de) *	2003-08-06	2011-02-15	Procter & Gamble	Verfahren zur herstellung eines wasserquellbaren materials mit beschichteten wasserquellbaren polymeren
CN1832984B (zh)	2003-08-06	2010-06-09	宝洁公司	已涂敷的水可溶胀材料
CA2534778C (fr) *	2003-08-06	2010-11-16	The Procter & Gamble Company	Structures absorbantes comprenant un materiau revetu gonflable dans l'eau
EP1518567B1 (fr)	2003-09-25	2017-06-28	The Procter & Gamble Company	Articles absorbants comprenant des zones d'acquisition et des particules revêtues et superabsorbantes
US9125965B2 (en) *	2004-02-24	2015-09-08	The Procter & Gamble Company	Superabsorbent polymers comprising direct covalent bonds between polymer chain segments and methods of making them
US8357727B2 (en)	2004-02-27	2013-01-22	Dow Global Technologies Llc	Durable foam of olefin polymers, methods of making foam and articles prepared from same
US7361694B2 (en) *	2004-02-27	2008-04-22	Dow Global Technologies Inc.	Durable foam of olefin polymers, methods of making foam and articles prepared from same
DE602004029569D1 (de) *	2004-07-20	2010-11-25	Procter & Gamble	Oberflächlich vernetzte superabsorbierende Partikeln und Verfahren zu ihrer Herstellung
US8080705B2 (en)	2004-07-28	2011-12-20	The Procter & Gamble Company	Superabsorbent polymers comprising direct covalent bonds between polymer chain segments and method of making them
EP1669394A1 (fr)	2004-12-10	2006-06-14	The Procter & Gamble Company	Particules polymères superabsorbantes ayant la réticulation de la surface et la propriété hydrophile améliorées et procédé pour leur préparation
RU2007132228A (ru) *	2005-01-28	2009-03-10	БАСФ Акциенгезельшафт (DE)	Применение эмульсий типа вода в воде полимеров в качестве загустителя в косметических композициях
MX2007009415A (es)	2005-02-04	2007-08-17	Procter & Gamble	Estructura absorbente con material absorbente de agua mejorado.
EP1736508A1 (fr)	2005-06-22	2006-12-27	Basf Aktiengesellschaft	Polymères formant des hydrogels avec perméabilité améliorée et haute capacité d'absorption
EP1757648A1 (fr)	2005-08-23	2007-02-28	Nippon Shokubai Co.,Ltd.	Procédé pour la réticulation en surface de particules de polymère super-absorbantes par rayonnement ultraviolet en présence d'acides de Bronsted
EP1757646A1 (fr)	2005-08-23	2007-02-28	The Procter and Gamble Company	Procédé pour la réticulation en surface de particules de polymère super-absorbantes par rayonnement ultraviolet
CA2620643C (fr) *	2005-08-23	2011-05-10	The Procter & Gamble Company	Articles absorbants comprenant des particules polymeriques superabsorbantes reticulees de surface produites selon un procede dans lequel est utilise un rayonnement ultraviolet extreme
EP1757647A1 (fr)	2005-08-23	2007-02-28	The Procter and Gamble Company	Procédé pour la réticulation en surface des particules de polymère super-absorbantes par rayonnement ultraviolet en présence d'acides de Bronsted
EP1757642A1 (fr)	2005-08-23	2007-02-28	The Procter and Gamble Company	Procédé pour la réticulation de la surface de particules polymères ultra-absorbantes par rayonnement ultraviolet sous vide
EP1757641A1 (fr) *	2005-08-23	2007-02-28	The Procter and Gamble Company	Procédé de réticulation de la surface de particules de polymères super-absorbants hautement neutralisées en utilisant des acides de Bronsted
EP1757643A1 (fr)	2005-08-23	2007-02-28	Nippon Shokubai Co.,Ltd.	Procédé pour la réticulation de la surface de particules polymères ultra-absorbantes par rayonnement ultraviolet sous vide
EP1757645A1 (fr)	2005-08-23	2007-02-28	Nippon Shokubai Co.,Ltd.	Procédé pour la réticulation en surface de particules de polymère super-absorbantes par rayonnement ultraviolet
WO2007024927A2 (fr) *	2005-08-23	2007-03-01	The Procter & Gamble Company	Articles absorbants comprenant des particules polymeriques superabsorbantes reticulees de surface produites selon un procede dans lequel est utilise un rayonnement ultraviolet extreme
CA2620170C (fr) *	2005-08-23	2011-04-12	The Procter & Gamble Company	Articles absorbants comprenant des particules polymeres superabsorbantes reticulees en surface obtenues par un procede utilisant un rayonnement ultraviolet et des acides de bronsted
US20070049886A1 (en) *	2005-08-31	2007-03-01	Kimberly-Clark Worldwide, Inc.	Absorbent web with improved integrity and methods for making the same
US7838610B2 (en) *	2005-09-30	2010-11-23	Nippon Shokubai Co., Ltd.	Ion-sensitive super-absorbent polymer
JP2007099845A (ja) *	2005-09-30	2007-04-19	Procter & Gamble Co	水性液吸収剤およびその製法
EP1948702A2 (fr)	2005-11-17	2008-07-30	The Procter and Gamble Company	Utilisation et application de copolymeres zwitterioniques definis
MX2008013041A (es)	2006-04-10	2008-10-17	Procter & Gamble	Un miembro absorbente que comprende una resina absorbente de agua modificada.
ATE554799T1 (de) *	2006-08-07	2012-05-15	Procter & Gamble	Absorbierende artikel, die superabsorbierende polymere und ein strahleninduziert hydrophiles material enthalten
US20080083377A1 (en) *	2006-10-04	2008-04-10	Marni Markell Hurwitz	Compact foldable animal litter pan with disposable waste collection sheets
US7748348B2 (en) *	2006-10-04	2010-07-06	I Did It, Inc.	Compact foldable animal litter pan with disposable adhesive waste collection sheets
US7824386B2 (en)	2006-10-26	2010-11-02	The Procter & Gamble Company	Method for using a disposable absorbent article as a swim pant
US7824387B2 (en)	2006-10-26	2010-11-02	The Procter & Gamble Company	Method for using a disposable absorbent article as training pant
US7766887B2 (en)	2006-11-13	2010-08-03	The Procter & Gamble Company	Method for making reusable disposable article
US20080114320A1 (en)	2006-11-13	2008-05-15	Theodora Beck	Absorbent articles having fluid partitioning characteristics and method for evaluating such characteristics
US7842020B2 (en)	2006-11-17	2010-11-30	I Did It, Inc.	Double diaper system
US20080179330A1 (en) *	2007-01-29	2008-07-31	Brooks Kerry G	Trash containment system
EP2121049B1 (fr) *	2007-02-22	2016-03-30	The Procter and Gamble Company	Procédé de traitement de surface d'un matériau particulaire au moyen d'un rayonnement électromagnétique
JP4994175B2 (ja) *	2007-09-28	2012-08-08	富士フイルム株式会社	平版印刷版原版、及びそれに用いる共重合体の製造方法
US20100093581A1 (en) *	2008-10-15	2010-04-15	Rubi Rose, Llc.	All Purpose Cleaning Compositions
ES2523722T3 (es)	2008-11-21	2014-12-01	Hercules Incorporated	Polímeros policarboxílicos hidrofóbicamente modificados no hidrocarbílicos
EP2277558B1 (fr)	2009-07-20	2014-07-02	The Procter and Gamble Company	Particules polymères superabsorbantes et procédés correspondants
EP2277557B1 (fr)	2009-07-20	2014-06-25	The Procter and Gamble Company	Particules polymères superabsorbantes enrobées et procédés correspondants
EP2477487A2 (fr)	2009-09-15	2012-07-25	Basf Se	Dispersions aqueuses contenant des antimicrobiens dans un réseau hybride
WO2011064153A1 (fr)	2009-11-26	2011-06-03	Basf Se	Utilisation de polyesters très ramifiés dans des formulations cosmétiques et dermatologiques
US20110123473A1 (en) *	2009-11-26	2011-05-26	Basf Se	Use of highly-branched polycarbonates in cosmetic and dermatological formulations
RU2012126264A (ru)	2009-11-26	2014-01-20	Басф Се	Применение высокоразветвленных поликарбонатов в косметических и дерматологических композициях
US8653321B2 (en) *	2010-02-25	2014-02-18	The Procter & Gamble Company	Method for determining the gel strength of a hydrogel
WO2011106490A2 (fr)	2010-02-25	2011-09-01	The Procter & Gamble Company	Procédé pour la détermination de la résistance de gel d'un hydrogel
EP2579835B1 (fr)	2010-06-11	2020-06-24	The Procter and Gamble Company	Compositions pour traitement de la peau
FR2961513B1 (fr) *	2010-06-22	2012-07-13	Soc Dexploitation De Produits Pour Les Industries Chimiques Seppic	Nouveau polymere epaississant de phases grasses sans monomere ionique
EP2447286A1 (fr)	2010-11-01	2012-05-02	The Procter & Gamble Company	Procédé utilisant un milieu supercritique pour produire des polymères
EP2732832A3 (fr)	2012-11-14	2015-07-01	Universitair Medisch Centrum Groningen (UMCG)	Dispositif d'administration de médicament comprenant un composé actif et un matériau polymère thermosensible
EP2907828A1 (fr)	2014-02-14	2015-08-19	Basf Se	Procédé de fabrication de copolymères VP/VI cationogènes-ampholytiques
MY176354A (en)	2014-05-05	2020-07-30	Lubrizol Advanced Mat Inc	Homogenous film compositions
KR102455927B1 (ko)	2014-07-09	2022-10-17	루브리졸 어드밴스드 머티어리얼스, 인코포레이티드	하이드로겔 조성물
US9631773B2 (en)	2014-08-26	2017-04-25	Nochar, Inc.	Shipping container having a flame retardant layer and a thermal blocking layer
US11207248B2 (en)	2014-11-10	2021-12-28	The Procter And Gamble Company	Personal care compositions with two benefit phases
WO2016077327A1 (fr)	2014-11-10	2016-05-19	The Procter & Gamble Company	Compositions de soins personnels comportant deux phases à effet bénéfique
US10966916B2 (en)	2014-11-10	2021-04-06	The Procter And Gamble Company	Personal care compositions
WO2016077329A1 (fr)	2014-11-10	2016-05-19	The Procter & Gamble Company	Compositions de soins personnels
ES2745696T3 (es)	2014-12-05	2020-03-03	Univ Florida	Impresión 3D utilizando materiales de cambio de fase como soporte
WO2016130953A1 (fr)	2015-02-13	2016-08-18	University Of Florida Research Foundation, Inc.	Système d'impression en 3d à grande vitesse destiné au remplacement d'une plaie ou d'un tissu
WO2016182969A1 (fr)	2015-05-08	2016-11-17	University Of Florida Research Foundation, Inc.	Milieu de croissance pour culture de cellules tridimensionnelle
US11027483B2 (en)	2015-09-03	2021-06-08	University Of Florida Research Foundation, Inc.	Valve incorporating temporary phase change material
JP2019501268A (ja)	2015-11-05	2019-01-17	ルブリゾルアドバンスドマテリアルズ，インコーポレイテッド	熱成形可能なデュアルネットワークヒドロゲル組成物
WO2017096263A1 (fr)	2015-12-04	2017-06-08	University Of Florida Research Foundation, Incorporated	Polymères réticulables ou fonctionnalisables pour l'impression 3d de matériaux mous
US11111339B2 (en)	2015-12-04	2021-09-07	Momentive Performance Materials Inc.	Polyacrylate salt, methods of preparation and applications for employing the same
US11147268B2 (en)	2015-12-10	2021-10-19	The Clorox Company	Food contact surface sanitizing liquid
US11124644B2 (en)	2016-09-01	2021-09-21	University Of Florida Research Foundation, Inc.	Organic microgel system for 3D printing of silicone structures
CN111065270A (zh)	2017-07-18	2020-04-24	阿格里麦蒂斯有限责任公司	L-草胺膦的生产方法
WO2019079409A1 (fr)	2017-10-20	2019-04-25	The Procter & Gamble Company	Nettoyant pour la peau en mousse aérosol
EP3697374B1 (fr)	2017-10-20	2022-02-16	The Procter & Gamble Company	Nettoyant moussant en aérosol pour la peau
CN109880001A (zh) *	2017-12-06	2019-06-14	万华化学（北京）有限公司	一种丙烯酸树脂的制备方法和由其制备的丙烯酸树脂及用途
CN111432892B (zh)	2017-12-08	2023-08-29	宝洁公司	筛选温和洁肤剂的方法
US11680241B2 (en)	2018-02-08	2023-06-20	University Of Florida Research Foundation, Inc.	Perfusion enabled bioreactors
WO2019157356A1 (fr)	2018-02-08	2019-08-15	University Of Florida Research Foundation	Bioréacteurs permettant la perfusion
CA3099546A1 (fr)	2018-06-13	2019-12-19	Star Liberty LLC	Kits et procedes d'elimination de produits pharmaceutiques liquides et de produits pharmaceutiques solides dissous
CN112449648B (zh) *	2018-07-26	2022-11-15	昭和电工材料株式会社	树脂组合物、储热材料及包括储热材料的物品
US11879119B2 (en)	2018-08-01	2024-01-23	University Of Florida Research Foundation, Inc.	Perfusion bioreactor driven by osmotic pressure gradients
CN113165879A (zh)	2018-11-20	2021-07-23	路博润公司	石墨烯的产生和组合物
EP3887824A1 (fr)	2018-11-29	2021-10-06	The Procter & Gamble Company	Méthodes de criblage de produits de soins personnels
CN117015565A (zh)	2021-03-05	2023-11-07	路博润先进材料公司	用于润湿和分散丙烯酸聚合物的方法
WO2023060083A1 (fr)	2021-10-05	2023-04-13	University Of Florida Research Foundation	Compositions, systèmes et procédés relatifs aux modèles tissulaires hépatiques tridimensionnels (3d) bio-imprimés
CN116004157B (zh) *	2022-08-15	2025-11-28	苏州柯燚半导体材料科技有限公司	一种丙烯酸酯分散液及其在压敏胶上的应用
WO2026043945A1 (fr)	2024-08-22	2026-02-26	The Lubrizol Corporation	Séparateur revêtu de céramique et adhésif

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2795564A (en) *	1953-05-13	1957-06-11	Rohm & Haas	Aqueous paint bases and water-base paints and process for preparing them
US2790736A (en) *	1955-01-31	1957-04-30	Rohm & Haas	Methods of making coated paper products and the products obtained
US2892791A (en) *	1956-02-03	1959-06-30	California Research Corp	Lubricant composition
US2892792A (en) *	1956-02-03	1959-06-30	California Research Corp	Lubricant composition
US3194777A (en) *	1956-05-14	1965-07-13	Pittsburgh Plate Glass Co	Coating compositions
US2892788A (en) *	1956-07-30	1959-06-30	California Research Corp	Lubricant composition
US3317493A (en) *	1963-11-05	1967-05-02	Du Pont	Terpolymer containing methyl methacrylate, 2-ethylhexyl acrylate and methacrylic acid and compositions containing same
US3575911A (en) *	1964-11-19	1971-04-20	Minnesota Mining & Mfg	Adhesives
US3577517A (en) *	1965-03-26	1971-05-04	Mitsubishi Rayon Co	Acrylic or methacrylic acid copolymer in resinous aerosol hair preparations
US3657175A (en) *	1969-06-26	1972-04-18	Standard Brands Chem Ind Inc	Carboxylic acid latices providing unique thickening and dispersing agents
US3954898A (en) *	1969-11-27	1976-05-04	Mitsui Toatsu Chemicals, Incorporated	Powder coating of epoxy resin, acrylic copolymer and tertiary amine
IL35515A0 (en) *	1970-05-13	1970-12-24	Israel American Technology Inc	A hydrophilic copolymer and a method for its preparation
GB1394990A (en) *	1971-08-12	1975-05-21	Hydrophilics Int Inc	Copolymers and compositions containing copolymers
US3957740A (en) *	1972-04-24	1976-05-18	Hydrophilics International, Inc.	Copolymers
FR2218351B1 (fr) *	1973-02-16	1976-05-14	Protex Manuf Prod Chimiq
US3970633A (en) *	1973-05-16	1976-07-20	Rohm And Haas Company	Thermosetting powder coatings composition
US3940351A (en) *	1974-07-02	1976-02-24	The B. F. Goodrich Company	Polymerization of carboxylic acid monomers and alkyl acrylate esters in chlorofluoroethane
CH606154A5 (fr) *	1974-07-02	1978-11-15	Goodrich Co B F

1977
- 1977-04-04 US US05/784,099 patent/US4062817A/en not_active Expired - Lifetime
- 1977-07-25 CA CA283,430A patent/CA1086447A/fr not_active Expired
- 1977-07-26 AU AU27328/77A patent/AU510453B2/en not_active Expired
- 1977-07-26 DK DK337777A patent/DK337777A/da not_active Application Discontinuation
- 1977-07-29 DE DE19772734298 patent/DE2734298A1/de not_active Withdrawn
- 1977-08-03 IT IT26465/77A patent/IT1085352B/it active
- 1977-08-04 SE SE7708882A patent/SE425974B/xx not_active IP Right Cessation
- 1977-08-05 GB GB32858/77A patent/GB1589975A/en not_active Expired
- 1977-08-08 NL NLAANVRAGE7708733,A patent/NL189674C/xx not_active IP Right Cessation
- 1977-08-15 JP JP9709477A patent/JPS53123490A/ja active Pending
- 1977-08-17 MX MX170268A patent/MX145592A/es unknown
- 1977-08-22 NO NO772912A patent/NO772912L/no unknown
- 1977-09-08 FR FR7727258A patent/FR2386565A1/fr active Granted
- 1977-09-16 BE BE180990A patent/BE858800A/fr not_active IP Right Cessation
1978
- 1978-01-01 CH CH946177A patent/CH636363A5/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
NL189674C (nl)	1993-06-16
FR2386565A1 (fr)	1978-11-03
GB1589975A (en)	1981-05-20
DE2734298A1 (de)	1978-10-05
US4062817A (en)	1977-12-13
DK337777A (da)	1978-10-05
SE7708882L (sv)	1978-10-05
CH636363A5 (de)	1983-05-31
NL189674B (nl)	1993-01-18
SE425974B (sv)	1982-11-29
JPS53123490A (en)	1978-10-27
CA1086447A (fr)	1980-09-23
AU510453B2 (en)	1980-06-26
IT1085352B (it)	1985-05-28
AU2732877A (en)	1979-02-01
FR2386565B1 (fr)	1984-05-25
BE858800A (fr)	1978-01-16
MX145592A (es)	1982-03-11
NL7708733A (nl)	1978-10-06

Publication	Publication Date	Title
NO772912L (no)	1978-10-05	Interpolymer.
US4190562A (en)	1980-02-26	Improved water absorbent copolymers of copolymerizable carboxylic acids and acrylic or methacrylic esters
US5712316A (en)	1998-01-27	Powder-form cross-linked polymers capable of absorbing aqueous liquids and body fluids, method of preparing them and their use
US4066583A (en)	1978-01-03	Flexible water absorbent polymer compositions comprising (a) unsaturated carboxylic acid, acrylic ester containing alkyl group 10-30 carbon atoms, additional monomer plus (b) aliphatic diol
JP2922216B2 (ja)	1999-07-19	高吸水性ポリマー製造法
RU2106153C1 (ru)	1998-03-10	Порошкообразная смола, способ ее получения, изделие
KR100351477B1 (ko)	2002-11-07	흡수성및방수성을가진감온성(感溫性)폴리머조성물
US5286827A (en)	1994-02-15	Superabsorbent crosslinked copolymers formed from an ampholytic ion pair (2-methacryloyloxyethyldimethylammonium cation (MEDMA)/sulfonate anion) copolymerized with other comonomers
RU2001126351A (ru)	2003-08-10	Порошкообразные, сшитые, абсорбирующие водные жидкости, а также кровь полимеры, способ их получения и их применение
JPH05132528A (ja)	1993-05-28	電解質水溶液吸収性重合体
JPS6136763B2 (fr)	1986-08-20
JPH10330433A (ja)	1998-12-15	水膨潤性親水性ポリマー組成物
GB2179663A (en)	1987-03-11	Absorptive resins
CA2043662C (fr)	1996-08-27	Copolymeres reticules ampholytiques superabsorbants, formes d'une paire d'ions
US5439983A (en)	1995-08-08	Grafted copolymers highly absorbent to aqueous electrolyte solutions
NO791464L (no)	1979-11-06	Fremgangsmaate til fremstilling av karboksylholdige polymerer
EP0055728A4 (fr)	1982-08-11	Interpolymeres hydrophiles d'acides acryliques et d'un acrylate.
JPH0323567B2 (fr)	1991-03-29
US5252690A (en)	1993-10-12	Superabsorbent polymers
JPH0420007B2 (fr)	1992-03-31
US5412052A (en)	1995-05-02	Grafted copolymers highly absorbent to aqueous electrolyte solutions
JP2927911B2 (ja)	1999-07-28	高吸水性ポリマーおよびその製造法
Buchholz	1990	Preparation and structure of polyacrylates
JP3141059B2 (ja)	2001-03-05	感温性吸水樹脂
JP2716485B2 (ja)	1998-02-18	高吸水性ポリマーの製造法