DE19921899A1 - Mikrobizide Copolymere - Google Patents

Mikrobizide Copolymere

Info

Publication number: DE19921899A1
Authority: DE; Germany
Prior art keywords: component; amino group; antimicrobial; monomers; copolymerization
Prior art date: 1999-05-12
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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE19921899A

Other languages

German (de)

English (en)

Inventor

Peter Ottersbach

Beate Kossmann

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.)

Creavis Gesellschaft fuer Technologie und Innovation mbH

Original Assignee

Creavis Gesellschaft fuer Technologie und Innovation mbH

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.)

1999-05-12

Filing date

1999-05-12

Publication date

2000-11-16

1999-05-12 Application filed by Creavis Gesellschaft fuer Technologie und Innovation mbH filed Critical Creavis Gesellschaft fuer Technologie und Innovation mbH

1999-05-12 Priority to DE19921899A priority Critical patent/DE19921899A1/de

2000-03-30 Priority to AU72363/00A priority patent/AU7236300A/en

2000-03-30 Priority to CN00810327A priority patent/CN1361797A/zh

2000-03-30 Priority to EP00929329A priority patent/EP1183293A1/de

2000-03-30 Priority to PCT/EP2000/002781 priority patent/WO2000069934A1/de

2000-03-30 Priority to JP2000618349A priority patent/JP2002544347A/ja

2000-11-16 Publication of DE19921899A1 publication Critical patent/DE19921899A1/de

2001-11-12 Priority to NO20015531A priority patent/NO20015531L/no

Status Withdrawn legal-status Critical Current

Links

239000000178 monomer Substances 0.000 title claims abstract description 50
230000000845 anti-microbial effect Effects 0.000 title claims abstract description 17
238000000576 coating method Methods 0.000 title claims description 11
239000003973 paint Substances 0.000 title claims description 5
229920001577 copolymer Polymers 0.000 title abstract description 16
125000003277 amino group Chemical group 0.000 title abstract description 6
239000002966 varnish Substances 0.000 title description 2
238000002360 preparation method Methods 0.000 claims abstract description 3
239000000758 substrate Substances 0.000 claims description 35
125000001931 aliphatic group Chemical group 0.000 claims description 25
229920002118 antimicrobial polymer Polymers 0.000 claims description 22
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 22
238000007334 copolymerization reaction Methods 0.000 claims description 21
238000000034 method Methods 0.000 claims description 18
230000005855 radiation Effects 0.000 claims description 15
229920000642 polymer Polymers 0.000 claims description 14
101000623895 Bos taurus Mucin-15 Proteins 0.000 claims description 12
238000010559 graft polymerization reaction Methods 0.000 claims description 9
125000004432 carbon atom Chemical group C* 0.000 claims description 8
238000004519 manufacturing process Methods 0.000 claims description 7
229910052757 nitrogen Inorganic materials 0.000 claims description 7
239000011248 coating agent Substances 0.000 claims description 6
125000004122 cyclic group Chemical group 0.000 claims description 6
125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
229910052760 oxygen Inorganic materials 0.000 claims description 6
125000004430 oxygen atom Chemical group O* 0.000 claims description 6
229920006395 saturated elastomer Polymers 0.000 claims description 6
229930195734 saturated hydrocarbon Natural products 0.000 claims description 6
125000004434 sulfur atom Chemical group 0.000 claims description 6
229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 6
230000008569 process Effects 0.000 claims description 5
239000004599 antimicrobial Substances 0.000 claims description 4
238000006385 ozonation reaction Methods 0.000 claims description 4
238000009832 plasma treatment Methods 0.000 claims description 4
238000003851 corona treatment Methods 0.000 claims description 3
239000011253 protective coating Substances 0.000 claims description 2
230000000379 polymerizing effect Effects 0.000 abstract description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
239000000047 product Substances 0.000 description 37
238000012360 testing method Methods 0.000 description 33
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 24
239000000725 suspension Substances 0.000 description 24
230000000813 microbial effect Effects 0.000 description 21
239000000203 mixture Substances 0.000 description 21
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
244000052616 bacterial pathogen Species 0.000 description 13
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 12
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
241000191967 Staphylococcus aureus Species 0.000 description 10
230000004913 activation Effects 0.000 description 9
-1 4-methylphenylamino Chemical group 0.000 description 8
230000003641 microbiacidal effect Effects 0.000 description 8
241000589517 Pseudomonas aeruginosa Species 0.000 description 7
241000894006 Bacteria Species 0.000 description 6
229910052786 argon Inorganic materials 0.000 description 6
238000001914 filtration Methods 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
238000003756 stirring Methods 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
235000013305 food Nutrition 0.000 description 5
JMSTYCQEPRPFBF-UHFFFAOYSA-N methyl 2-methoxy-2-(prop-2-enoylamino)acetate Chemical compound COC(=O)C(OC)NC(=O)C=C JMSTYCQEPRPFBF-UHFFFAOYSA-N 0.000 description 5
239000002904 solvent Substances 0.000 description 5
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
238000013459 approach Methods 0.000 description 4
BCDUBXMSQFRJJJ-UHFFFAOYSA-N 2-(propanoylamino)prop-2-enoic acid Chemical compound CCC(=O)NC(=C)C(O)=O BCDUBXMSQFRJJJ-UHFFFAOYSA-N 0.000 description 3
BEWCNXNIQCLWHP-UHFFFAOYSA-N 2-(tert-butylamino)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCNC(C)(C)C BEWCNXNIQCLWHP-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
230000001580 bacterial effect Effects 0.000 description 3
239000003999 initiator Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
239000011159 matrix material Substances 0.000 description 3
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
238000004806 packaging method and process Methods 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000004033 plastic Substances 0.000 description 3
229920000307 polymer substrate Polymers 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
229920002614 Polyether block amide Polymers 0.000 description 2
239000004793 Polystyrene Substances 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
239000012965 benzophenone Substances 0.000 description 2
230000005670 electromagnetic radiation Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
229920000578 graft copolymer Polymers 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
239000012528 membrane Substances 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
125000005397 methacrylic acid ester group Chemical group 0.000 description 2
SMWNFFKPVLVOQQ-UHFFFAOYSA-N methyl 2-acetamidoprop-2-enoate Chemical compound COC(=O)C(=C)NC(C)=O SMWNFFKPVLVOQQ-UHFFFAOYSA-N 0.000 description 2
XFHJDMUEHUHAJW-UHFFFAOYSA-N n-tert-butylprop-2-enamide Chemical compound CC(C)(C)NC(=O)C=C XFHJDMUEHUHAJW-UHFFFAOYSA-N 0.000 description 2
239000003504 photosensitizing agent Substances 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
229920000193 polymethacrylate Polymers 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
229920001343 polytetrafluoroethylene Polymers 0.000 description 2
239000004810 polytetrafluoroethylene Substances 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
239000004800 polyvinyl chloride Substances 0.000 description 2
229920000915 polyvinyl chloride Polymers 0.000 description 2
238000012545 processing Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004753 textile Substances 0.000 description 2
231100000331 toxic Toxicity 0.000 description 2
230000002588 toxic effect Effects 0.000 description 2
LPUCKLOWOWADAC-UHFFFAOYSA-M tributylstannyl 2-methylprop-2-enoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C(C)=C LPUCKLOWOWADAC-UHFFFAOYSA-M 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
IECWHJOALGVHPA-UHFFFAOYSA-N 2-hydroxy-n-prop-2-enylbenzamide Chemical compound OC1=CC=CC=C1C(=O)NCC=C IECWHJOALGVHPA-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
TZTADYBXPPAGNG-UHFFFAOYSA-N 3-(ethylamino)but-2-enoic acid Chemical compound CCNC(C)=CC(O)=O TZTADYBXPPAGNG-UHFFFAOYSA-N 0.000 description 1
MGZAGXMLBKSKRX-UHFFFAOYSA-N 3-(methylamino)-1-phenylprop-2-en-1-one Chemical compound CNC=CC(=O)C1=CC=CC=C1 MGZAGXMLBKSKRX-UHFFFAOYSA-N 0.000 description 1
SQNWFKZOFAOCHM-UHFFFAOYSA-N 3-azaniumyl-2-methylprop-2-enoate Chemical class [NH3+]C=C(C)C([O-])=O SQNWFKZOFAOCHM-UHFFFAOYSA-N 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
241000222178 Candida tropicalis Species 0.000 description 1
GUTLYIVDDKVIGB-OUBTZVSYSA-N Cobalt-60 Chemical compound [60Co] GUTLYIVDDKVIGB-OUBTZVSYSA-N 0.000 description 1
241000588724 Escherichia coli Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
229930194542 Keto Natural products 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
240000005384 Rhizopus oryzae Species 0.000 description 1
235000013752 Rhizopus oryzae Nutrition 0.000 description 1
241000248418 Tetrahymena pyriformis Species 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
150000008062 acetophenones Chemical class 0.000 description 1
150000003926 acrylamides Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
150000008360 acrylonitriles Chemical class 0.000 description 1
125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
230000006978 adaptation Effects 0.000 description 1
239000003570 air Substances 0.000 description 1
238000004378 air conditioning Methods 0.000 description 1
125000003172 aldehyde group Chemical group 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
RRCPAXJDDNWJBI-UHFFFAOYSA-N alprenolol hydrochloride Chemical compound [H+].[Cl-].CC(C)NCC(O)COC1=CC=CC=C1CC=C RRCPAXJDDNWJBI-UHFFFAOYSA-N 0.000 description 1
150000003868 ammonium compounds Chemical class 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000012300 argon atmosphere Substances 0.000 description 1
230000004888 barrier function Effects 0.000 description 1
235000013361 beverage Nutrition 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
239000003139 biocide Substances 0.000 description 1
PVEOYINWKBTPIZ-UHFFFAOYSA-N but-3-enoic acid Chemical compound OC(=O)CC=C PVEOYINWKBTPIZ-UHFFFAOYSA-N 0.000 description 1
239000013043 chemical agent Substances 0.000 description 1
YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
230000001427 coherent effect Effects 0.000 description 1
210000001520 comb Anatomy 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
239000007857 degradation product Substances 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000009189 diving Effects 0.000 description 1
238000005553 drilling Methods 0.000 description 1
239000003651 drinking water Substances 0.000 description 1
235000020188 drinking water Nutrition 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000003628 erosive effect Effects 0.000 description 1
IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
MRDCWMLXFWVCIR-UHFFFAOYSA-N ethyl 3-(ethylamino)but-2-enoate Chemical compound CCNC(C)=CC(=O)OCC MRDCWMLXFWVCIR-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000003925 fat Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000002737 fuel gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
230000036541 health Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
239000007943 implant Substances 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
238000002955 isolation Methods 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000000155 melt Substances 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000013508 migration Methods 0.000 description 1
230000005012 migration Effects 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
210000003097 mucus Anatomy 0.000 description 1
YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
229920003052 natural elastomer Polymers 0.000 description 1
229920001194 natural rubber Polymers 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
230000000474 nursing effect Effects 0.000 description 1
239000003921 oil Substances 0.000 description 1
238000013021 overheating Methods 0.000 description 1
125000004043 oxo group Chemical group O=* 0.000 description 1
239000005022 packaging material Substances 0.000 description 1
238000010422 painting Methods 0.000 description 1
UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
150000002976 peresters Chemical class 0.000 description 1
125000005385 peroxodisulfate group Chemical group 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920003055 poly(ester-imide) Polymers 0.000 description 1
229920002492 poly(sulfone) Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920006149 polyester-amide block copolymer Polymers 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
IEFBNOCPIBPPMK-UHFFFAOYSA-N propyl 2-hydroxy-3-(3-triethoxysilylpropylamino)prop-2-enoate Chemical compound CCCOC(=O)C(O)=CNCCC[Si](OCC)(OCC)OCC IEFBNOCPIBPPMK-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
238000011160 research Methods 0.000 description 1
238000007789 sealing Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
230000037072 sun protection Effects 0.000 description 1
230000008961 swelling Effects 0.000 description 1
230000009182 swimming Effects 0.000 description 1
229920003051 synthetic elastomer Polymers 0.000 description 1
239000005061 synthetic rubber Substances 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 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
229920002554 vinyl polymer Polymers 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/10—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to inorganic materials
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/34—Shaped forms, e.g. sheets, not provided for in any other sub-group of this main group
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/46—Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L27/54—Biologically active materials, e.g. therapeutic substances
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- 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
- C08F257/00—Macromolecular compounds obtained by polymerising monomers on to polymers of aromatic monomers as defined in group C08F12/00
- C08F257/02—Macromolecular compounds obtained by polymerising monomers on to polymers of aromatic monomers as defined in group C08F12/00 on to polymers of styrene or alkyl-substituted styrenes
- 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
- C08F259/00—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/006—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers provided for in C08G18/00
- 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
- C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
- 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
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/003—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/20—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
- A61L2300/204—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials with nitrogen-containing functional groups, e.g. aminoxides, nitriles, guanidines
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/404—Biocides, antimicrobial agents, antiseptic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/45—Mixtures of two or more drugs, e.g. synergistic mixtures

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Medicinal Chemistry (AREA)
Wood Science & Technology (AREA)
Polymers & Plastics (AREA)
General Health & Medical Sciences (AREA)
Materials Engineering (AREA)
Zoology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Inorganic Chemistry (AREA)
Environmental Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
Epidemiology (AREA)
Transplantation (AREA)
Oral & Maxillofacial Surgery (AREA)
Dermatology (AREA)
Molecular Biology (AREA)
Biomedical Technology (AREA)
Hematology (AREA)
Toxicology (AREA)
Materials For Medical Uses (AREA)
Paints Or Removers (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Graft Or Block Polymers (AREA)

DE19921899A 1999-05-12 1999-05-12 Mikrobizide Copolymere Withdrawn DE19921899A1 (de)

Priority Applications (7)

Application Number	Priority Date	Filing Date	Title
DE19921899A DE19921899A1 (de)	1999-05-12	1999-05-12	Mikrobizide Copolymere
AU72363/00A AU7236300A (en)	1999-05-12	2000-03-30	Microbicidal copolymers
CN00810327A CN1361797A (zh)	1999-05-12	2000-03-30	杀微生物共聚物
EP00929329A EP1183293A1 (de)	1999-05-12	2000-03-30	Mikrobizide copolymere
PCT/EP2000/002781 WO2000069934A1 (de)	1999-05-12	2000-03-30	Mikrobizide copolymere
JP2000618349A JP2002544347A (ja)	1999-05-12	2000-03-30	抗微生物性コポリマー
NO20015531A NO20015531L (no)	1999-05-12	2001-11-12	Mikrobedrepende kopolymerer

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19921899A DE19921899A1 (de)	1999-05-12	1999-05-12	Mikrobizide Copolymere

Publications (1)

Publication Number	Publication Date
DE19921899A1 true DE19921899A1 (de)	2000-11-16

Family

ID=7907834

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19921899A Withdrawn DE19921899A1 (de)	1999-05-12	1999-05-12	Mikrobizide Copolymere

Country Status (7)

Country	Link
EP (1)	EP1183293A1 (zh)
JP (1)	JP2002544347A (zh)
CN (1)	CN1361797A (zh)
AU (1)	AU7236300A (zh)
DE (1)	DE19921899A1 (zh)
NO (1)	NO20015531L (zh)
WO (1)	WO2000069934A1 (zh)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2002046279A2 (de) *	2000-12-09	2002-06-13	Creavis Gesellschaft Für Technologie Und Innovation Mbh	Verfahren zur thermisch unterstützten antimikrobiellen oberflächenausrüstung
WO2002070573A1 (de) *	2001-03-07	2002-09-12	Creavis Gesellschaft Für Technologie Und Innovation Mbh	Mikrobizide trennsysteme
EP2036930A1 (en) *	2007-09-12	2009-03-18	Institut National De La Recherche Agronomique (Inra)	Copolymer-grafted polyolefin substrate having antimicrobial properties and method for grafting
CN102325446A (zh) *	2008-12-29	2012-01-18	3M创新有限公司	通过乙烯胺-乙烯醇共聚物的衍生化获得的涂层表面抗微生物共聚物

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10117106A1 (de) *	2001-04-06	2002-10-17	Creavis Tech & Innovation Gmbh	Antimikrobielle Konservierungssysteme für Lebensmittel
WO2015146196A1 (ja) *	2014-03-28	2015-10-01	株式会社日本触媒	新規重合体、樹脂組成物、樹脂成形体、および新規重合体の製造方法
JP6809777B2 (ja) *	2015-03-27	2021-01-06	株式会社日本触媒	熱可塑性重合体、樹脂組成物、樹脂成形体、光学部材、および熱可塑性重合体の製造方法
JP6846105B2 (ja) *	2015-08-20	2021-03-24	株式会社日本触媒	重合体、樹脂組成物および樹脂成形体ならびに重合体の製造方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19709075A1 (de) *	1997-03-06	1998-09-10	Huels Chemische Werke Ag	Verfahren zur Herstellung antimikrobieller Kunststoffe
DK0872512T3 (da) *	1997-04-14	2001-08-27	Degussa	Fremgangsmåde til modificering af overfladen af polymersubstrater ved podningspolymerisation

1999
- 1999-05-12 DE DE19921899A patent/DE19921899A1/de not_active Withdrawn
2000
- 2000-03-30 CN CN00810327A patent/CN1361797A/zh active Pending
- 2000-03-30 JP JP2000618349A patent/JP2002544347A/ja active Pending
- 2000-03-30 WO PCT/EP2000/002781 patent/WO2000069934A1/de not_active Application Discontinuation
- 2000-03-30 EP EP00929329A patent/EP1183293A1/de not_active Withdrawn
- 2000-03-30 AU AU72363/00A patent/AU7236300A/en not_active Abandoned
2001
- 2001-11-12 NO NO20015531A patent/NO20015531L/no unknown

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2002046279A2 (de) *	2000-12-09	2002-06-13	Creavis Gesellschaft Für Technologie Und Innovation Mbh	Verfahren zur thermisch unterstützten antimikrobiellen oberflächenausrüstung
WO2002046279A3 (de) *	2000-12-09	2002-08-22	Creavis Tech & Innovation Gmbh	Verfahren zur thermisch unterstützten antimikrobiellen oberflächenausrüstung
WO2002070573A1 (de) *	2001-03-07	2002-09-12	Creavis Gesellschaft Für Technologie Und Innovation Mbh	Mikrobizide trennsysteme
EP2036930A1 (en) *	2007-09-12	2009-03-18	Institut National De La Recherche Agronomique (Inra)	Copolymer-grafted polyolefin substrate having antimicrobial properties and method for grafting
WO2009034152A1 (en) *	2007-09-12	2009-03-19	Institut National De La Recherche Agronomique - Inra	Copolymer-grafted polyolefin substrate having antimicrobial properties and method for grafting
CN102325446A (zh) *	2008-12-29	2012-01-18	3M创新有限公司	通过乙烯胺-乙烯醇共聚物的衍生化获得的涂层表面抗微生物共聚物
CN102325446B (zh) *	2008-12-29	2014-07-09	3M创新有限公司	通过乙烯胺-乙烯醇共聚物的衍生化获得的涂层表面抗微生物共聚物

Also Published As

Publication number	Publication date
WO2000069934A1 (de)	2000-11-23
AU7236300A (en)	2000-12-05
NO20015531D0 (no)	2001-11-12
CN1361797A (zh)	2002-07-31
JP2002544347A (ja)	2002-12-24
EP1183293A1 (de)	2002-03-06
NO20015531L (no)	2002-01-11

Publication	Publication Date	Title
DE19709075A1 (de)	1998-09-10	Verfahren zur Herstellung antimikrobieller Kunststoffe
DE10022406A1 (de)	2001-11-15	Antimikrobielle, Aminofunktionalisierte Copolymere
DE19921904A1 (de)	2000-11-16	Verfahren zur Herstellung inhärent mikrobizider Polymeroberflächen
DE19921898A1 (de)	2000-11-16	Verfahren zur Herstellung inhärent mikrobizider Polymeroberflächen
WO2001072859A1 (de)	2001-10-04	Antimikrobielle beschichtungen, enthaltend polymere von acrylsubstituierten alkylsulfonsäuren
DE19921900A1 (de)	2000-11-16	Verfahren zur Herstellung inhärent mikrobizider Polymeroberflächen
WO2001016193A1 (de)	2001-03-08	Copolymere von acryloyloxyalkylaminoverbindungen
WO2001087998A2 (de)	2001-11-22	Antimikrobielle polymere und polymerblends aus polymeren alkylacrylamiden
EP1228112A1 (de)	2002-08-07	Copolymere von acryloylaminoalkylverbindungen
DE19940023A1 (de)	2001-03-01	Copolymere des Aminopropylvinylethers
DE19921895A1 (de)	2000-11-16	Antimikrobielle Copolymere
DE19921899A1 (de)	2000-11-16	Mikrobizide Copolymere
DE19921903A1 (de)	2000-11-16	Mikrobizide Copolymere
WO2001062810A1 (en)	2001-08-30	Copolymers of allylphosphonium salts
DE19921902A1 (de)	2000-11-16	Mikrobizide Copolymere
DE19921897A1 (de)	2000-11-16	Verfahren zur Herstellung inhärent mikrobizider Polymeroberflächen
DE19940697A1 (de)	2001-03-01	Copolymere von Acryloyloxyalkylammoniumsalzen
DE19943344A1 (de)	2001-03-15	Copolymere von Dialkylaminoalkylacrylamiden
DE19952222A1 (de)	2001-05-03	Copolymere von Acryloylaminoalkylammoniumsalzen
DE19952221A1 (de)	2001-05-03	Copolymere von Acryloyloxyalkyldialkylaminen
DE10123195A1 (de)	2002-11-14	Elutionsfreie antimikrobielle Polymere
DE19955992A1 (de)	2001-05-23	Copolymere von Acryloyloxyalkylbenzophenonammoniumsalzen
WO2004033568A1 (de)	2004-04-22	Antimikrobielle beschichtungen und ein verfahren zu deren herstellung

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2005-03-17	8139	Disposal/non-payment of the annual fee