CA2527362A1 - Esters (meth)acryliques de glycols alkylene-ylene et leur utilisation - Google Patents

Esters (meth)acryliques de glycols alkylene-ylene et leur utilisation Download PDF

Info

Publication number: CA2527362A1
Authority: CA; Canada
Prior art keywords: weight; reaction mixture; equal; ester; meth
Prior art date: 2003-06-06
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.): Abandoned

Application number

CA002527362A

Other languages

English (en)

Inventor

Ulrich Riegel

Thomas Daniel

Matthias Weismantel

Mark Elliott

Rudiger Funk

Reinhold Schwalm

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF SE

Original Assignee

Individual

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.)

2003-06-06

Filing date

2004-06-04

Publication date

2004-12-16

2003-06-06 Priority claimed from PCT/EP2003/005953 external-priority patent/WO2003104300A1/fr

2003-12-11 Priority claimed from DE2003158369 external-priority patent/DE10358369A1/de

2004-06-04 Application filed by Individual filed Critical Individual

2004-12-16 Publication of CA2527362A1 publication Critical patent/CA2527362A1/fr

Status Abandoned legal-status Critical Current

Links

LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 title claims description 53
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 title claims description 22
-1 acrylic ester Chemical class 0.000 title abstract description 43
239000011541 reaction mixture Substances 0.000 claims abstract description 76
150000002148 esters Chemical class 0.000 claims abstract description 61
238000004519 manufacturing process Methods 0.000 claims abstract description 23
239000000017 hydrogel Substances 0.000 claims description 81
229920000642 polymer Polymers 0.000 claims description 79
239000004971 Cross linker Substances 0.000 claims description 72
238000000034 method Methods 0.000 claims description 71
239000000203 mixture Substances 0.000 claims description 70
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 68
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 56
230000008569 process Effects 0.000 claims description 49
238000006243 chemical reaction Methods 0.000 claims description 45
238000005886 esterification reaction Methods 0.000 claims description 43
230000032050 esterification Effects 0.000 claims description 42
239000002904 solvent Substances 0.000 claims description 40
239000002253 acid Substances 0.000 claims description 30
239000000178 monomer Substances 0.000 claims description 30
239000003054 catalyst Substances 0.000 claims description 23
238000006116 polymerization reaction Methods 0.000 claims description 23
238000001035 drying Methods 0.000 claims description 18
239000012530 fluid Substances 0.000 claims description 18
239000003112 inhibitor Substances 0.000 claims description 15
150000001875 compounds Chemical class 0.000 claims description 14
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
238000004821 distillation Methods 0.000 claims description 12
229920000058 polyacrylate Polymers 0.000 claims description 10
150000002009 diols Chemical class 0.000 claims description 7
239000003085 diluting agent Substances 0.000 claims description 6
239000003999 initiator Substances 0.000 claims description 6
230000003472 neutralizing effect Effects 0.000 claims description 6
238000007873 sieving Methods 0.000 claims description 6
239000007858 starting material Substances 0.000 claims description 6
239000000654 additive Substances 0.000 claims description 5
230000000996 additive effect Effects 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
238000000227 grinding Methods 0.000 claims description 4
239000004568 cement Substances 0.000 claims description 3
239000005022 packaging material Substances 0.000 claims description 3
239000003973 paint Substances 0.000 claims description 3
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 2
239000006185 dispersion Substances 0.000 claims description 2
239000004745 nonwoven fabric Substances 0.000 claims description 2
239000002994 raw material Substances 0.000 claims description 2
230000000379 polymerizing effect Effects 0.000 claims 2
150000002334 glycols Chemical class 0.000 abstract description 3
239000000835 fiber Substances 0.000 description 64
239000002250 absorbent Substances 0.000 description 37
230000002745 absorbent Effects 0.000 description 36
239000000499 gel Substances 0.000 description 33
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 30
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 26
239000000243 solution Substances 0.000 description 25
239000002657 fibrous material Substances 0.000 description 24
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 19
238000006386 neutralization reaction Methods 0.000 description 19
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
238000010276 construction Methods 0.000 description 18
239000000463 material Substances 0.000 description 18
239000007789 gas Substances 0.000 description 17
238000004132 cross linking Methods 0.000 description 16
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 15
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
238000010438 heat treatment Methods 0.000 description 15
229920003043 Cellulose fiber Polymers 0.000 description 14
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
238000010521 absorption reaction Methods 0.000 description 14
230000002829 reductive effect Effects 0.000 description 14
239000000126 substance Substances 0.000 description 14
229920002994 synthetic fiber Polymers 0.000 description 14
NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 13
239000002245 particle Substances 0.000 description 13
150000003254 radicals Chemical class 0.000 description 13
238000010626 work up procedure Methods 0.000 description 13
239000002585 base Substances 0.000 description 12
239000003795 chemical substances by application Substances 0.000 description 12
239000007788 liquid Substances 0.000 description 12
229920003023 plastic Polymers 0.000 description 12
239000004033 plastic Substances 0.000 description 12
239000000047 product Substances 0.000 description 12
235000002639 sodium chloride Nutrition 0.000 description 12
239000012209 synthetic fiber Substances 0.000 description 12
229920001169 thermoplastic Polymers 0.000 description 12
238000007792 addition Methods 0.000 description 11
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 10
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
239000004416 thermosoftening plastic Substances 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
229920002678 cellulose Polymers 0.000 description 9
239000001913 cellulose Substances 0.000 description 9
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239000010408 film Substances 0.000 description 9
229910052757 nitrogen Inorganic materials 0.000 description 9
239000001301 oxygen Substances 0.000 description 9
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238000012856 packing Methods 0.000 description 9
229920000728 polyester Polymers 0.000 description 9
239000003381 stabilizer Substances 0.000 description 9
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 8
229920005372 Plexiglas® Polymers 0.000 description 8
239000004698 Polyethylene Substances 0.000 description 8
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
238000001816 cooling Methods 0.000 description 8
238000001914 filtration Methods 0.000 description 8
150000002500 ions Chemical class 0.000 description 8
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 8
229920000573 polyethylene Polymers 0.000 description 8
229920001223 polyethylene glycol Polymers 0.000 description 8
HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 8
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
206010021639 Incontinence Diseases 0.000 description 7
239000002202 Polyethylene glycol Substances 0.000 description 7
229940048053 acrylate Drugs 0.000 description 7
125000004386 diacrylate group Chemical group 0.000 description 7
239000011780 sodium chloride Substances 0.000 description 7
ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
239000004743 Polypropylene Substances 0.000 description 6
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
238000012644 addition polymerization Methods 0.000 description 6
239000000853 adhesive Substances 0.000 description 6
230000001070 adhesive effect Effects 0.000 description 6
239000008346 aqueous phase Substances 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 6
238000010533 azeotropic distillation Methods 0.000 description 6
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 6
229920001155 polypropylene Polymers 0.000 description 6
239000011148 porous material Substances 0.000 description 6
238000007127 saponification reaction Methods 0.000 description 6
QQOMQLYQAXGHSU-UHFFFAOYSA-N 236TMPh Natural products CC1=CC=C(C)C(O)=C1C QQOMQLYQAXGHSU-UHFFFAOYSA-N 0.000 description 5
239000007983 Tris buffer Substances 0.000 description 5
150000007513 acids Chemical class 0.000 description 5
150000001298 alcohols Chemical class 0.000 description 5
210000001124 body fluid Anatomy 0.000 description 5
239000010839 body fluid Substances 0.000 description 5
238000000576 coating method Methods 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
238000007334 copolymerization reaction Methods 0.000 description 5
239000012632 extractable Substances 0.000 description 5
238000000605 extraction Methods 0.000 description 5
239000011261 inert gas Substances 0.000 description 5
239000011159 matrix material Substances 0.000 description 5
235000013372 meat Nutrition 0.000 description 5
239000005020 polyethylene terephthalate Substances 0.000 description 5
239000000843 powder Substances 0.000 description 5
238000010526 radical polymerization reaction Methods 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
238000005507 spraying Methods 0.000 description 5
239000011732 tocopherol Substances 0.000 description 5
BXJGUBZTZWCMEX-UHFFFAOYSA-N 2,3-dimethylbenzene-1,4-diol Chemical compound CC1=C(C)C(O)=CC=C1O BXJGUBZTZWCMEX-UHFFFAOYSA-N 0.000 description 4
PGSWEKYNAOWQDF-UHFFFAOYSA-N 3-methylcatechol Chemical compound CC1=CC=CC(O)=C1O PGSWEKYNAOWQDF-UHFFFAOYSA-N 0.000 description 4
ZBCATMYQYDCTIZ-UHFFFAOYSA-N 4-methylcatechol Chemical compound CC1=CC=C(O)C(O)=C1 ZBCATMYQYDCTIZ-UHFFFAOYSA-N 0.000 description 4
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 4
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 4
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
239000004793 Polystyrene Substances 0.000 description 4
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 4
229920000297 Rayon Polymers 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
229920002472 Starch Polymers 0.000 description 4
239000003708 ampul Substances 0.000 description 4
150000008064 anhydrides Chemical class 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
235000010354 butylated hydroxytoluene Nutrition 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
238000009833 condensation Methods 0.000 description 4
230000005494 condensation Effects 0.000 description 4
238000013461 design Methods 0.000 description 4
238000009826 distribution Methods 0.000 description 4
239000003814 drug Substances 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 4
LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 4
JVTZFYYHCGSXJV-UHFFFAOYSA-N isovanillin Chemical compound COC1=CC=C(C=O)C=C1O JVTZFYYHCGSXJV-UHFFFAOYSA-N 0.000 description 4
GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
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238000002360 preparation method Methods 0.000 description 4
239000002964 rayon Substances 0.000 description 4
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235000019698 starch Nutrition 0.000 description 4
KEQHJBNSCLWCAE-UHFFFAOYSA-N thymoquinone Chemical compound CC(C)C1=CC(=O)C(C)=CC1=O KEQHJBNSCLWCAE-UHFFFAOYSA-N 0.000 description 4
229960001295 tocopherol Drugs 0.000 description 4
CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 4
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125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
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229920000742 Cotton Polymers 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
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239000004952 Polyamide Substances 0.000 description 3
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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 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 description 3
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WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 2
KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 2
AUFZRCJENRSRLY-UHFFFAOYSA-N 2,3,5-trimethylhydroquinone Chemical compound CC1=CC(O)=C(C)C(C)=C1O AUFZRCJENRSRLY-UHFFFAOYSA-N 0.000 description 2
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235000007079 manganese sulphate Nutrition 0.000 description 1
UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 description 1
AWTNYZMRDAMOGW-UHFFFAOYSA-L manganese(2+);dicarbamodithioate Chemical compound [Mn+2].NC([S-])=S.NC([S-])=S AWTNYZMRDAMOGW-UHFFFAOYSA-L 0.000 description 1
SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 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
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
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WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
238000010327 methods by industry Methods 0.000 description 1
NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
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HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
229960000990 monobenzone Drugs 0.000 description 1
238000000465 moulding Methods 0.000 description 1
KXQXILJJTWHMRW-UHFFFAOYSA-N n,n'-bis(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl)hexanediamide Chemical compound C1C(C)(C)N(O)C(C)(C)CC1NC(=O)CCCCC(=O)NC1CC(C)(C)N(O)C(C)(C)C1 KXQXILJJTWHMRW-UHFFFAOYSA-N 0.000 description 1
FSWDLYNGJBGFJH-UHFFFAOYSA-N n,n'-di-2-butyl-1,4-phenylenediamine Chemical compound CCC(C)NC1=CC=C(NC(C)CC)C=C1 FSWDLYNGJBGFJH-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
UCMYJOPIPDLTRT-UHFFFAOYSA-N n,n-diethyl-2-nitrosoaniline Chemical compound CCN(CC)C1=CC=CC=C1N=O UCMYJOPIPDLTRT-UHFFFAOYSA-N 0.000 description 1
DZCCLNYLUGNUKQ-UHFFFAOYSA-N n-(4-nitrosophenyl)hydroxylamine Chemical compound ONC1=CC=C(N=O)C=C1 DZCCLNYLUGNUKQ-UHFFFAOYSA-N 0.000 description 1
MJOANTDRRCETRJ-UHFFFAOYSA-N n-[6-[formyl-(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl)amino]hexyl]-n-(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl)formamide Chemical compound C1C(C)(C)N(O)C(C)(C)CC1N(C=O)CCCCCCN(C=O)C1CC(C)(C)N(O)C(C)(C)C1 MJOANTDRRCETRJ-UHFFFAOYSA-N 0.000 description 1
PNLUGRYDUHRLOF-UHFFFAOYSA-N n-ethenyl-n-methylacetamide Chemical compound C=CN(C)C(C)=O PNLUGRYDUHRLOF-UHFFFAOYSA-N 0.000 description 1
RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 description 1
ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
229940078494 nickel acetate Drugs 0.000 description 1
QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
BQHTWZRFOSRCCH-UHFFFAOYSA-L nickel(2+);dicarbamodithioate Chemical compound [Ni+2].NC([S-])=S.NC([S-])=S BQHTWZRFOSRCCH-UHFFFAOYSA-L 0.000 description 1
229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
150000002826 nitrites Chemical class 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
229920001542 oligosaccharide Polymers 0.000 description 1
150000002482 oligosaccharides Chemical class 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
238000005457 optimization Methods 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
238000006053 organic reaction Methods 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
150000002926 oxygen Chemical class 0.000 description 1
RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
230000036961 partial effect Effects 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
150000004986 phenylenediamines Chemical class 0.000 description 1
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229940068918 polyethylene glycol 400 Drugs 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
238000012667 polymer degradation Methods 0.000 description 1
229920006254 polymer film Polymers 0.000 description 1
239000003505 polymerization initiator Substances 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920006306 polyurethane fiber Polymers 0.000 description 1
229920002620 polyvinyl fluoride Polymers 0.000 description 1
239000011736 potassium bicarbonate Substances 0.000 description 1
235000015497 potassium bicarbonate Nutrition 0.000 description 1
229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
235000011181 potassium carbonates Nutrition 0.000 description 1
TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
244000144977 poultry Species 0.000 description 1
235000013594 poultry meat Nutrition 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
230000002028 premature Effects 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
RZKYDQNMAUSEDZ-UHFFFAOYSA-N prop-2-enylphosphonic acid Chemical compound OP(O)(=O)CC=C RZKYDQNMAUSEDZ-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
238000011002 quantification Methods 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000013557 residual solvent Substances 0.000 description 1
230000000552 rheumatic effect Effects 0.000 description 1
230000002000 scavenging effect Effects 0.000 description 1
150000003333 secondary alcohols Chemical class 0.000 description 1
230000035939 shock Effects 0.000 description 1
238000001577 simple distillation Methods 0.000 description 1
229940047670 sodium acrylate Drugs 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
229940048086 sodium pyrophosphate Drugs 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000011122 softwood Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003892 spreading Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
150000003455 sulfinic acids Chemical class 0.000 description 1
150000003464 sulfur compounds Chemical class 0.000 description 1
230000000475 sunscreen effect Effects 0.000 description 1
239000000516 sunscreening agent Substances 0.000 description 1
239000004583 superabsorbent polymers (SAPs) Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
230000008961 swelling Effects 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
238000012360 testing method Methods 0.000 description 1
DGQOCLATAPFASR-UHFFFAOYSA-N tetrahydroxy-1,4-benzoquinone Chemical compound OC1=C(O)C(=O)C(O)=C(O)C1=O DGQOCLATAPFASR-UHFFFAOYSA-N 0.000 description 1
235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
KRAHLZAGPKKBSW-UHFFFAOYSA-N tetrasodium;dioxidophosphanyl phosphite Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])OP([O-])[O-] KRAHLZAGPKKBSW-UHFFFAOYSA-N 0.000 description 1
238000009757 thermoplastic moulding Methods 0.000 description 1
229920002397 thermoplastic olefin Polymers 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
235000019149 tocopherols Nutrition 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
238000012549 training Methods 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
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
238000005809 transesterification reaction Methods 0.000 description 1
VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
230000005641 tunneling Effects 0.000 description 1
238000002604 ultrasonography Methods 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
239000006200 vaporizer Substances 0.000 description 1
239000002966 varnish Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
238000005303 weighing Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
229910001928 zirconium oxide Inorganic materials 0.000 description 1
QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
- C08G65/3322—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof acyclic
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Macromonomer-Based Addition Polymer (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Polyethers (AREA)

CA002527362A 2003-06-06 2004-06-04 Esters (meth)acryliques de glycols alkylene-ylene et leur utilisation Abandoned CA2527362A1 (fr)

Applications Claiming Priority (5)

Application Number	Priority Date	Filing Date	Title
EPPCT/EP/03/05953		2003-06-06
PCT/EP2003/005953 WO2003104300A1 (fr)	2002-06-01	2003-06-06	Esters (meth)acryliques de trimethylolpropane polyalcoxyle
DE10358369.6		2003-12-11
DE2003158369 DE10358369A1 (de)	2003-06-06	2003-12-11	(Meth)acrylester von Alkylenylenglycolen und deren Verwendung
PCT/EP2004/006033 WO2004108795A1 (fr)	2003-06-06	2004-06-04	Esters (meth)acryliques de glycols alkylene-ylene et leur utilisation

Publications (1)

Publication Number	Publication Date
CA2527362A1 true CA2527362A1 (fr)	2004-12-16

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ID=33512405

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002527362A Abandoned CA2527362A1 (fr)	2003-06-06	2004-06-04	Esters (meth)acryliques de glycols alkylene-ylene et leur utilisation

Country Status (6)

Country	Link
EP (1)	EP1636291A1 (fr)
JP (1)	JP2006527179A (fr)
BR (1)	BRPI0410899A (fr)
CA (1)	CA2527362A1 (fr)
MX (1)	MXPA05012802A (fr)
WO (1)	WO2004108795A1 (fr)

Families Citing this family (11)

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Publication number	Priority date	Publication date	Assignee	Title
WO2005095498A1 (fr) *	2004-03-30	2005-10-13	Basf Aktiengesellschaft	Procede perfectionne de fabrication de polymeres superabsorbants
DE102005002412A1 (de) *	2005-01-18	2006-07-27	Basf Ag	Verfahren zur Herstellung von Polymeren durch Sprühpolymerisation
DE102006008998A1 (de)	2006-02-23	2007-08-30	Röhm Gmbh	Verfahren zur Herstellung von Alkoxypolyoxyalkylen(meth)acrylaten
EP1996493A2 (fr)	2006-03-14	2008-12-03	Basf Se	Procédé pour transporter de manière pneumatique des particules polymères absorbant l'eau
CN101405207B (zh) *	2006-03-14	2013-07-17	巴斯夫欧洲公司	吸水性聚合物颗粒的气动输送方法
DE102006039420A1 (de)	2006-08-23	2008-02-28	Evonik Rohmax Additves Gmbh	Verfahren zur Herstellung von Methacrylatestern
US8334352B2 (en)	2007-09-21	2012-12-18	Dsm Ip Assets B.V.	Branched polyesteramine acrylate
DE102008040214A1 (de)	2008-07-07	2010-01-14	Evonik Röhm Gmbh	Verfahren zur Herstellung von Polyalkylenglykoldi(meth)acrylaten
KR102429543B1 (ko) *	2018-10-18	2022-08-04	주식회사 엘지화학	신규한 가교제 화합물 및 이를 이용하여 제조되는 고흡수성 수지
KR102614264B1 (ko) *	2019-09-19	2023-12-18	주식회사 엘지화학	에스터화 생성물의 중화/수분리조 및 에스터화 생성물의 중화/수분리 방법
CN112661638B (zh) *	2020-12-18	2022-07-15	宁波坚锋新材料有限公司	一种增韧中间体及其制备方法以及用于3d打印的增韧驱蚊高分子生物降解复合材料

Family Cites Families (9)

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JPS6024807B2 (ja) *	1979-02-19	1985-06-14	昭和電工株式会社	高吸水性ヒドロゲルの製造方法
EP0559476B1 (fr) *	1992-03-05	1997-07-16	Nippon Shokubai Co., Ltd.	Méthode de préparation d'une résine absorbante
JP3466222B2 (ja) *	1992-03-05	2003-11-10	株式会社日本触媒	吸水性樹脂の製造方法
JP3631545B2 (ja) *	1995-11-22	2005-03-23	株式会社巴川製紙所	可逆性記録方法
JP3281307B2 (ja) *	1997-12-24	2002-05-13	日立化成工業株式会社	感光性樹脂組成物、これを用いた感光性エレメント、感光性樹脂組成物の層の積層方法、感光性樹脂組成物層積層基板及び感光性樹脂組成物の層の硬化方法
JP4450909B2 (ja) *	1999-11-17	2010-04-14	花王株式会社	セメント分散剤の製造方法
KR100537085B1 (ko) *	2000-06-22	2005-12-16	히다치 가세고교 가부시끼가이샤	감광성 수지조성물, 이것을 사용한 감광성 엘리먼트,레지스트 패턴의 제조방법 및 프린트 배선판의 제조방법
CN1250622C (zh) *	2001-01-19	2006-04-12	巴斯福股份公司	吸水剂、其制备方法及其应用
EP1270530A1 (fr) *	2001-06-20	2003-01-02	Cognis Iberia, S.L.	Retardateur de prise pour plâtre

2004
- 2004-06-04 JP JP2006508273A patent/JP2006527179A/ja active Pending
- 2004-06-04 EP EP04736051A patent/EP1636291A1/fr not_active Withdrawn
- 2004-06-04 WO PCT/EP2004/006033 patent/WO2004108795A1/fr active Application Filing
- 2004-06-04 CA CA002527362A patent/CA2527362A1/fr not_active Abandoned
- 2004-06-04 BR BRPI0410899-0A patent/BRPI0410899A/pt not_active IP Right Cessation
- 2004-06-04 MX MXPA05012802A patent/MXPA05012802A/es unknown

Also Published As

Publication number	Publication date
EP1636291A1 (fr)	2006-03-22
WO2004108795A1 (fr)	2004-12-16
JP2006527179A (ja)	2006-11-30
BRPI0410899A (pt)	2006-07-04
MXPA05012802A (es)	2006-02-22

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KR20050020984A (ko)	2005-03-04	폴리알콕실화 트리메틸올프로판의 (메트)아크릴산에스테르

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