NZ309676A - Coatable biocidal compositions comprising an acrylate emulsion polymer comprising acrylate or methacrylate and carboxylic acid monomers; and a metal salt complexing agent - Google Patents
Coatable biocidal compositions comprising an acrylate emulsion polymer comprising acrylate or methacrylate and carboxylic acid monomers; and a metal salt complexing agentInfo
- Publication number
- NZ309676A NZ309676A NZ309676A NZ30967696A NZ309676A NZ 309676 A NZ309676 A NZ 309676A NZ 309676 A NZ309676 A NZ 309676A NZ 30967696 A NZ30967696 A NZ 30967696A NZ 309676 A NZ309676 A NZ 309676A
- Authority
- NZ
- New Zealand
- Prior art keywords
- acrylate
- composition
- coating
- compositions
- group
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 134
- 230000003115 biocidal effect Effects 0.000 title claims description 50
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 title claims description 29
- 239000000178 monomer Substances 0.000 title claims description 21
- 150000003839 salts Chemical class 0.000 title claims description 17
- 239000004908 Emulsion polymer Substances 0.000 title claims description 16
- 229910052751 metal Inorganic materials 0.000 title claims description 14
- 239000002184 metal Substances 0.000 title claims description 14
- 239000008139 complexing agent Substances 0.000 title claims description 13
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 title claims description 8
- 150000001735 carboxylic acids Chemical class 0.000 title description 2
- 239000000758 substrate Substances 0.000 claims description 95
- 238000000576 coating method Methods 0.000 claims description 62
- 239000003139 biocide Substances 0.000 claims description 48
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 48
- 239000011248 coating agent Substances 0.000 claims description 41
- 239000000839 emulsion Substances 0.000 claims description 33
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 24
- 125000004122 cyclic group Chemical group 0.000 claims description 24
- 230000000052 comparative effect Effects 0.000 claims description 22
- 229910000077 silane Inorganic materials 0.000 claims description 22
- -1 tri- ethylene glycol ethers Chemical class 0.000 claims description 14
- 230000001464 adherent effect Effects 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 238000012360 testing method Methods 0.000 claims description 12
- 125000003178 carboxy group Chemical class [H]OC(*)=O 0.000 claims description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 9
- 229910052725 zinc Inorganic materials 0.000 claims description 9
- 239000011701 zinc Substances 0.000 claims description 9
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 8
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 238000005406 washing Methods 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 230000000845 anti-microbial effect Effects 0.000 claims description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 6
- 230000002538 fungal effect Effects 0.000 claims description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 6
- 150000002989 phenols Chemical class 0.000 claims description 6
- ODIUACFRPDQOPA-UHFFFAOYSA-M C(C=C/C(=O)[O-])(=O)[O-].[Zn+].[NH4+] Chemical compound C(C=C/C(=O)[O-])(=O)[O-].[Zn+].[NH4+] ODIUACFRPDQOPA-UHFFFAOYSA-M 0.000 claims description 5
- RWPOLKFFARHZDK-UHFFFAOYSA-N NC1=CC=CC=C1.N.[Ca+2] Chemical compound NC1=CC=CC=C1.N.[Ca+2] RWPOLKFFARHZDK-UHFFFAOYSA-N 0.000 claims description 5
- MUHUIJPSGRCRFX-UHFFFAOYSA-M [Zn+].C([O-])([O-])=O.[NH4+] Chemical compound [Zn+].C([O-])([O-])=O.[NH4+] MUHUIJPSGRCRFX-UHFFFAOYSA-M 0.000 claims description 5
- SXGBQDIIBBUDKN-UHFFFAOYSA-N acetic acid;azane;zinc Chemical compound [NH4+].[Zn].CC([O-])=O SXGBQDIIBBUDKN-UHFFFAOYSA-N 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- GIYDISLTIIILLG-UHFFFAOYSA-N azane;prop-2-enoic acid;zinc Chemical compound [NH4+].[Zn].[O-]C(=O)C=C GIYDISLTIIILLG-UHFFFAOYSA-N 0.000 claims description 5
- 239000006184 cosolvent Substances 0.000 claims description 5
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 4
- BEZPOYJGECASSD-UHFFFAOYSA-N CC(ON)=O.N.[Zn+2] Chemical compound CC(ON)=O.N.[Zn+2] BEZPOYJGECASSD-UHFFFAOYSA-N 0.000 claims description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 4
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical class O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 3
- 150000001346 alkyl aryl ethers Chemical class 0.000 claims description 3
- DIOLOCSXUMYFJN-UHFFFAOYSA-N calcium;azane Chemical compound N.[Ca+2] DIOLOCSXUMYFJN-UHFFFAOYSA-N 0.000 claims description 3
- 235000013985 cinnamic acid Nutrition 0.000 claims description 3
- WBYWAXJHAXSJNI-UHFFFAOYSA-N cinnamic acid group Chemical class C(C=CC1=CC=CC=C1)(=O)O WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 3
- 150000008056 dicarboxyimides Chemical class 0.000 claims description 3
- 125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 claims description 3
- 150000004053 quinones Chemical class 0.000 claims description 3
- 150000003457 sulfones Chemical class 0.000 claims description 3
- 150000004867 thiadiazoles Chemical class 0.000 claims description 3
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 claims description 3
- PNFOZEDBTQHPPH-UHFFFAOYSA-M C([O-])([O-])=O.C(CN)N.[Ca+].[NH4+] Chemical compound C([O-])([O-])=O.C(CN)N.[Ca+].[NH4+] PNFOZEDBTQHPPH-UHFFFAOYSA-M 0.000 claims description 2
- 150000004891 diazines Chemical class 0.000 claims description 2
- 125000004188 dichlorophenyl group Chemical group 0.000 claims description 2
- 239000012990 dithiocarbamate Substances 0.000 claims description 2
- 150000004659 dithiocarbamates Chemical class 0.000 claims description 2
- ZJXZSIYSNXKHEA-UHFFFAOYSA-N ethyl dihydrogen phosphate Chemical class CCOP(O)(O)=O ZJXZSIYSNXKHEA-UHFFFAOYSA-N 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 238000012986 modification Methods 0.000 claims description 2
- 150000003567 thiocyanates Chemical class 0.000 claims description 2
- KEBUEWXZQBMCNB-UHFFFAOYSA-N 1h-benzimidazol-2-yl carbamate Chemical class C1=CC=C2NC(OC(=O)N)=NC2=C1 KEBUEWXZQBMCNB-UHFFFAOYSA-N 0.000 claims 2
- 229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 claims 2
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 claims 2
- GHEQMRDSHPGZIK-UHFFFAOYSA-N FC=1C(=C(C=CC1)N(C(=O)NC(C1=CC=CC=C1)=O)Cl)F Chemical compound FC=1C(=C(C=CC1)N(C(=O)NC(C1=CC=CC=C1)=O)Cl)F GHEQMRDSHPGZIK-UHFFFAOYSA-N 0.000 claims 2
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 2
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 150000003852 triazoles Chemical class 0.000 claims 2
- UUIVKBHZENILKB-UHFFFAOYSA-N 2,2-dibromo-2-cyanoacetamide Chemical compound NC(=O)C(Br)(Br)C#N UUIVKBHZENILKB-UHFFFAOYSA-N 0.000 claims 1
- VDGRKHYRTPJTLO-UHFFFAOYSA-N ClOC(C(Cl)(Cl)Cl)(C1=CC=CC=C1)Cl Chemical compound ClOC(C(Cl)(Cl)Cl)(C1=CC=CC=C1)Cl VDGRKHYRTPJTLO-UHFFFAOYSA-N 0.000 claims 1
- NSEQHAPSDIEVCD-UHFFFAOYSA-N N.[Zn+2] Chemical compound N.[Zn+2] NSEQHAPSDIEVCD-UHFFFAOYSA-N 0.000 claims 1
- 230000000536 complexating effect Effects 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000000232 haloalkynyl group Chemical group 0.000 claims 1
- 230000002035 prolonged effect Effects 0.000 claims 1
- 150000003918 triazines Chemical class 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 description 24
- 239000011440 grout Substances 0.000 description 18
- 239000004014 plasticizer Substances 0.000 description 12
- 238000001035 drying Methods 0.000 description 11
- 239000000919 ceramic Substances 0.000 description 10
- 150000004756 silanes Chemical class 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 239000001993 wax Substances 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000004816 latex Substances 0.000 description 6
- 229920000126 latex Polymers 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 230000028070 sporulation Effects 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 238000013270 controlled release Methods 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000003755 preservative agent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 230000000813 microbial effect Effects 0.000 description 4
- 239000004209 oxidized polyethylene wax Substances 0.000 description 4
- 235000013873 oxidized polyethylene wax Nutrition 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 241000233866 Fungi Species 0.000 description 3
- 239000003619 algicide Substances 0.000 description 3
- 230000002421 anti-septic effect Effects 0.000 description 3
- 239000000645 desinfectant Substances 0.000 description 3
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000002070 germicidal effect Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005065 mining Methods 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- WTLBZVNBAKMVDP-UHFFFAOYSA-N tris(2-butoxyethyl) phosphate Chemical compound CCCCOCCOP(=O)(OCCOCCCC)OCCOCCCC WTLBZVNBAKMVDP-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical compound COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000004599 antimicrobial Substances 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- SKKTUOZKZKCGTB-UHFFFAOYSA-N butyl carbamate Chemical compound CCCCOC(N)=O SKKTUOZKZKCGTB-UHFFFAOYSA-N 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000011152 fibreglass Substances 0.000 description 2
- 230000005923 long-lasting effect Effects 0.000 description 2
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 2
- 150000001282 organosilanes Chemical class 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- YYDNBUBMBZRNQQ-UHFFFAOYSA-N 1-methyl-4-methylsulfonylbenzene Chemical compound CC1=CC=C(S(C)(=O)=O)C=C1 YYDNBUBMBZRNQQ-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- HFOCAQPWSXBFFN-UHFFFAOYSA-N 2-methylsulfonylbenzaldehyde Chemical compound CS(=O)(=O)C1=CC=CC=C1C=O HFOCAQPWSXBFFN-UHFFFAOYSA-N 0.000 description 1
- QYYMDNHUJFIDDQ-UHFFFAOYSA-N 5-chloro-2-methyl-1,2-thiazol-3-one;2-methyl-1,2-thiazol-3-one Chemical compound CN1SC=CC1=O.CN1SC(Cl)=CC1=O QYYMDNHUJFIDDQ-UHFFFAOYSA-N 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 241000223678 Aureobasidium pullulans Species 0.000 description 1
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000221955 Chaetomium Species 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229920001651 Cyanoacrylate Polymers 0.000 description 1
- 102100020746 Dolichol-phosphate mannosyltransferase subunit 1 Human genes 0.000 description 1
- 101000932202 Homo sapiens Dolichol-phosphate mannosyltransferase subunit 1 Proteins 0.000 description 1
- PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000606507 Talaromyces pinophilus Species 0.000 description 1
- 241001149558 Trichoderma virens Species 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229940064004 antiseptic throat preparations Drugs 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000003609 aryl vinyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000008047 benzoylureas Chemical class 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- NLCKLZIHJQEMCU-UHFFFAOYSA-N cyano prop-2-enoate Chemical class C=CC(=O)OC#N NLCKLZIHJQEMCU-UHFFFAOYSA-N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- HHICRQHZPBOQPI-UHFFFAOYSA-L diazanium;zinc;dicarbonate Chemical compound [NH4+].[NH4+].[Zn+2].[O-]C([O-])=O.[O-]C([O-])=O HHICRQHZPBOQPI-UHFFFAOYSA-L 0.000 description 1
- 229960002380 dibutyl phthalate Drugs 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000000539 dimer Chemical class 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- PQIOSYKVBBWRRI-UHFFFAOYSA-N methylphosphonyl difluoride Chemical group CP(F)(F)=O PQIOSYKVBBWRRI-UHFFFAOYSA-N 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- XJTVQSAAHBCSBG-UHFFFAOYSA-N n-[chloro(phenyl)carbamoyl]benzamide Chemical compound C=1C=CC=CC=1N(Cl)C(=O)NC(=O)C1=CC=CC=C1 XJTVQSAAHBCSBG-UHFFFAOYSA-N 0.000 description 1
- 239000006199 nebulizer Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000010422 painting Methods 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
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- OSIVISXRDMXJQR-UHFFFAOYSA-M potassium;2-[ethyl(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctylsulfonyl)amino]acetate Chemical compound [K+].[O-]C(=O)CN(CC)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F OSIVISXRDMXJQR-UHFFFAOYSA-M 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 229910052726 zirconium Inorganic materials 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/062—Copolymers with monomers not covered by C09D133/06
- C09D133/064—Copolymers with monomers not covered by C09D133/06 containing anhydride, COOH or COOM groups, with M being metal or onium-cation
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing groups
-
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
-
- 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
- C09D143/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium, or a metal; Coating compositions based on derivatives of such polymers
- C09D143/04—Homopolymers or copolymers of monomers containing silicon
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/14—Paints containing biocides, e.g. fungicides, insecticides or pesticides
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- Paints Or Removers (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/502,166 US5585407A (en) | 1995-07-13 | 1995-07-13 | Water-based coatable compositions comprising reaction products of acrylic emulsion polymers with organoalkoxysilanes |
| PCT/US1996/009540 WO1997003135A1 (en) | 1995-07-13 | 1996-06-07 | Coatable biocidal compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ309676A true NZ309676A (en) | 1999-09-29 |
Family
ID=23996644
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ309676A NZ309676A (en) | 1995-07-13 | 1996-06-07 | Coatable biocidal compositions comprising an acrylate emulsion polymer comprising acrylate or methacrylate and carboxylic acid monomers; and a metal salt complexing agent |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5585407A (enExample) |
| EP (1) | EP0861302B1 (enExample) |
| JP (1) | JPH11508941A (enExample) |
| KR (1) | KR100433867B1 (enExample) |
| CN (1) | CN1148424C (enExample) |
| AU (1) | AU709129B2 (enExample) |
| BR (1) | BR9609609A (enExample) |
| NZ (1) | NZ309676A (enExample) |
| WO (1) | WO1997003135A1 (enExample) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1248268A (zh) * | 1997-01-15 | 2000-03-22 | 伊斯曼化学公司 | 水性氢化硅可交联胶乳组合物和其制备方法 |
| US5891966A (en) * | 1997-12-11 | 1999-04-06 | Eastman Chemical Company | Waterborne silicon hydride crosslinkable latex compositions and methods of preparing the same |
| US5786282A (en) * | 1997-02-25 | 1998-07-28 | Barnhardt Manufacturing Company | Opened wet processed intermediate natural fiber product suitable for formation into end use fiber products with long-lasting antimicrobial properties and method |
| ES2327369T3 (es) | 1998-02-12 | 2009-10-28 | Surfacine Development Company, Llc | Compuestos desinfectantes que proporcionan accion biocida prolongada. |
| DE19814133A1 (de) * | 1998-03-30 | 1999-10-07 | Espe Dental Ag | Selbstdesinfizierende Kunststoffe und ihre Verwendung im dentalen und dentaltechnischen Bereich |
| US6042877A (en) * | 1998-07-28 | 2000-03-28 | 3M Innovative Properties Company | Method for the manufacture of anti-microbial articles |
| JP2000119587A (ja) * | 1998-10-20 | 2000-04-25 | Clariant Polymer Kk | コーティング組成物 |
| US6221976B1 (en) | 1999-01-25 | 2001-04-24 | The Dow Chemical Company | Polymers containing partially neutralized silanols |
| US6420455B1 (en) | 1999-06-18 | 2002-07-16 | 3M Innovative Properties Company | Antimicrobial composition containing photosensitizers articles, and methods of use |
| US6432396B1 (en) | 2000-07-06 | 2002-08-13 | 3M Innovative Properties Company | Limiting the presence of microorganisms using polymer-bound metal-containing compositions |
| US7459167B1 (en) | 2000-07-27 | 2008-12-02 | 3M Innovative Properties Company | Biocidal polyurethane compositions and methods of use |
| US20030108700A1 (en) * | 2001-11-21 | 2003-06-12 | 3M Innovative Properties Company | Plastic shipping and storage containers and composition and method therefore |
| US20100160445A1 (en) * | 2002-01-17 | 2010-06-24 | Carlson Paul E | Synergistic Mixtures of OPP and DGH |
| US7262222B2 (en) * | 2002-01-17 | 2007-08-28 | Verichem, Inc. | Synergistic mixtures of o-phenylphenol and other nitrogen and aldehyde microbiocides |
| KR20040038041A (ko) * | 2002-10-31 | 2004-05-08 | 에스케이케미칼주식회사 | 살균제 조성물 및 이를 이용한 살균방법 |
| US6897191B2 (en) | 2003-04-30 | 2005-05-24 | Specialty Construction Brands, Inc. | Disinfecting, antimicrobial sealing compositions and methods of using the same |
| EP1667741B1 (en) * | 2003-09-08 | 2009-10-07 | Ethicon, Inc. | Cyanoacrylate monomer formulation containing diiodomethyl-p-tolylsulfone |
| US7902140B1 (en) | 2003-10-21 | 2011-03-08 | Bissell Homecare, Inc. | Carpet cleaning with fungicide |
| WO2006028491A1 (en) * | 2004-02-13 | 2006-03-16 | University Of Florida | Biocides based on silanol terminated silanes and siloxanes |
| WO2006031736A2 (en) * | 2004-09-13 | 2006-03-23 | Horsehead Corp. | Bacteria and mold resistant wallboard |
| US7484261B2 (en) | 2004-09-30 | 2009-02-03 | Kimberly-Clark Worldwide, Inc. | Spot cleaner |
| US20070009695A1 (en) * | 2005-07-07 | 2007-01-11 | Lancer Partnership, Ltd. | Method and apparatus for a mold barrier |
| US8124169B2 (en) | 2005-12-14 | 2012-02-28 | 3M Innovative Properties Company | Antimicrobial coating system |
| US9247736B2 (en) | 2005-12-14 | 2016-02-02 | 3M Innovative Properties Company | Antimicrobial adhesive films |
| US9668476B2 (en) * | 2006-02-23 | 2017-06-06 | Lanxess Corporation | Removable antimicrobial coating compositions and methods of use |
| EP1991624A2 (en) * | 2006-02-23 | 2008-11-19 | E.I. Du Pont De Nemours And Company | Removable antimicrobial coating compositions and methods of use |
| US7585919B2 (en) * | 2006-09-26 | 2009-09-08 | 3M Innovative Properties Company | Polymer derived from monomers with long-chain aliphatic, poly(oxyalkylene) and substrate-reactive groups |
| EP2342282B1 (en) * | 2008-09-26 | 2016-12-28 | 3M Innovative Properties Company | Antimicrobial and antifouling polymeric materials |
| US20110177146A1 (en) * | 2009-07-27 | 2011-07-21 | E. I. Du Pont De Nemours And Company | Removable antimicrobial coating compositions containing cationic rheology agent and methods of use |
| US20110182959A1 (en) | 2009-07-27 | 2011-07-28 | E.I. Du Pont De Nemours And Company. | Removable antimicrobial coating compositions containing acid-activated rheology agent and methods of use |
| US20120148751A1 (en) | 2010-12-14 | 2012-06-14 | Ecolab Usa Inc. | Wear resistant antimicrobial compositions and methods of use |
| EP2468825A1 (en) | 2010-12-21 | 2012-06-27 | Akzo Nobel Coatings International B.V. | Antifouling coating composition |
| US9580574B2 (en) | 2012-12-12 | 2017-02-28 | Galata Chemicals Llc | Bio-based biocide compositions and methods of preserving therewith |
| CN104893380A (zh) * | 2015-05-18 | 2015-09-09 | 苏州市贝克生物科技有限公司 | 一种医用防霉涂料及其制备方法 |
| CN104893379A (zh) * | 2015-05-18 | 2015-09-09 | 苏州市贝克生物科技有限公司 | 一种医用快干杀菌防霉涂料及其制备方法 |
| CN104893456A (zh) * | 2015-05-18 | 2015-09-09 | 苏州市贝克生物科技有限公司 | 一种医用杀菌防霉涂料及其制备方法 |
| CN110114453A (zh) * | 2016-09-08 | 2019-08-09 | 莫尔豪斯医学院 | 清洁组合物，其制造方法和使用 |
| GB201708025D0 (en) * | 2017-05-18 | 2017-07-05 | Clearstream Tech Ltd | A laminate membrane, an implant comprising the laminate membrane and a method of manufacturing the same |
| US20190230929A1 (en) * | 2018-01-30 | 2019-08-01 | W.M. Barr & Company, Inc. | Composition for residual sanitization |
| RU2687356C1 (ru) * | 2018-04-13 | 2019-05-13 | Общество С Ограниченной Ответственностью "Лаборатория Био Зет" | Состав для придания антимикробных свойств продуктам или материалам |
| JP7324720B2 (ja) * | 2020-01-27 | 2023-08-10 | 三菱鉛筆株式会社 | 抗菌粒子水分散体 |
| US12342824B2 (en) | 2020-04-28 | 2025-07-01 | Apex Biomaterials Inc. | Metal-infused antimicrobial material and method of preparation thereof |
| WO2023075664A1 (en) | 2021-10-26 | 2023-05-04 | Rise Research Institutes of Sweden AB | A disinfectant film-forming composition and a dry disinfectant film formed on a surface from the film forming composition |
| CN116535914A (zh) * | 2023-04-26 | 2023-08-04 | 广东美涂士建材股份有限公司 | 一种耐磨抗菌涂料及其制备方法 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL139174B (nl) * | 1963-12-31 | 1973-06-15 | Geigy Ag J R | Werkwijze voor het bereiden van triamino-s-triazinederivaten, geschikt voor het bereiden van oppervlakteveredelingsmiddelen en werkwijze voor het bereiden van oppervlakteveredelingsmiddelen die deze verbindingen bevatten, alsmede voorwerpen die met deze oppervlakteveredelingsmiddelen behandeld zijn. |
| US3666698A (en) * | 1970-12-14 | 1972-05-30 | Sherwin Williams Co | Water-soluble polyester resin containing phenylindan dicarboxylic acid |
| US3837875A (en) * | 1973-01-19 | 1974-09-24 | J Murphy | Composition for cleaning, sealing, preserving, protecting and beautifying host materials |
| JPS5319345B2 (enExample) * | 1974-05-17 | 1978-06-20 | ||
| US3976501A (en) * | 1974-09-18 | 1976-08-24 | Blue Maurice R | Process for cleaning and polishing a floor |
| US4340520A (en) * | 1980-06-27 | 1982-07-20 | Union Carbide Corporation | Polyester aminoorganosilane salt/polyalkylene oxide compositions for improved glass fiber treatment |
| US4340524A (en) * | 1980-06-30 | 1982-07-20 | Union Carbide Corporation | Water-resistant latex sealants |
| US4500337A (en) * | 1980-09-03 | 1985-02-19 | Young Robert W | Adherent controlled release microbiocides containing hydrolyzable silanes and organic titanium compounds |
| US4500339A (en) * | 1980-09-03 | 1985-02-19 | Young Robert W | Adherent controlled release microbiocides containing hydrolyzable silanes |
| US4601954A (en) * | 1984-03-30 | 1986-07-22 | Servicemaster Industries, Inc. | Disinfectant formulation |
| JPS6172071A (ja) * | 1984-09-17 | 1986-04-14 | Yuuhoo Chem Kk | 被覆剤組成物 |
| US5154920A (en) * | 1985-03-13 | 1992-10-13 | Ecolab Inc. | Disinfectant polymeric coatings for hard surfaces |
| US4818536A (en) * | 1986-06-05 | 1989-04-04 | The Dow Chemical Company | Emulsfiable polymer concentrate controlled delivery and release system |
| US5061485A (en) * | 1987-05-12 | 1991-10-29 | Ecolab Inc. | Disinfectant polymeric coatings for hard surfaces |
| JP2600343B2 (ja) * | 1988-10-28 | 1997-04-16 | ダイキン工業株式会社 | 防菌防黴剤組成物 |
| US5089205A (en) * | 1989-09-25 | 1992-02-18 | Becton, Dickinson And Company | Process for producing medical devices having antimicrobial properties |
| US5234974A (en) * | 1990-07-26 | 1993-08-10 | S. C. Johnson & Son, Inc. | Alkali-soluble hydrophilic polymer coatings |
| JP2517785B2 (ja) * | 1990-08-02 | 1996-07-24 | 信越化学工業株式会社 | 含浸性防水剤組成物 |
| US5118534A (en) * | 1991-02-07 | 1992-06-02 | The Dow Chemical Company | Alkylthioethanamine carbamic acid derivatives and their use in biocidal compositions |
| FR2684107B1 (fr) * | 1991-11-27 | 1995-06-23 | Rhone Poulenc Chimie | Dispersions aqueuses de polymeres styrene-acrylate carboxyle et leurs utilisations comme liant dans des compositions adhesives et de revetement. |
| KR950018342A (ko) * | 1993-12-15 | 1995-07-22 | 윌리엄 이. 램버트 3세 | 백악질 기질에 대한 코팅제의 접착력을 개선시키는 혼합조성물 |
-
1995
- 1995-07-13 US US08/502,166 patent/US5585407A/en not_active Expired - Lifetime
-
1996
- 1996-06-07 AU AU59902/96A patent/AU709129B2/en not_active Ceased
- 1996-06-07 WO PCT/US1996/009540 patent/WO1997003135A1/en not_active Ceased
- 1996-06-07 EP EP96917266A patent/EP0861302B1/en not_active Expired - Lifetime
- 1996-06-07 BR BR9609609A patent/BR9609609A/pt not_active IP Right Cessation
- 1996-06-07 CN CNB961954426A patent/CN1148424C/zh not_active Expired - Fee Related
- 1996-06-07 KR KR10-1998-0700207A patent/KR100433867B1/ko not_active Expired - Fee Related
- 1996-06-07 NZ NZ309676A patent/NZ309676A/en unknown
- 1996-06-07 JP JP9505806A patent/JPH11508941A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| AU5990296A (en) | 1997-02-10 |
| MX9800314A (es) | 1998-07-31 |
| US5585407A (en) | 1996-12-17 |
| KR19990028905A (ko) | 1999-04-15 |
| HK1015816A1 (en) | 1999-10-22 |
| KR100433867B1 (ko) | 2004-12-17 |
| BR9609609A (pt) | 1999-05-25 |
| CN1190422A (zh) | 1998-08-12 |
| EP0861302A1 (en) | 1998-09-02 |
| EP0861302B1 (en) | 2001-11-07 |
| AU709129B2 (en) | 1999-08-19 |
| CN1148424C (zh) | 2004-05-05 |
| WO1997003135A1 (en) | 1997-01-30 |
| JPH11508941A (ja) | 1999-08-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU709129B2 (en) | Coatable biocidal compositions | |
| US6727309B1 (en) | Floor finish composition | |
| CA2937827C (en) | Aqueous surface coating composition and modified particles | |
| TW200808850A (en) | Water-based polyurethane floor coating composition | |
| JP2007016201A (ja) | 非反応性の研磨剤固体粒子および有機シラン四級化合物を含有し界面活性剤を含まない洗浄性かつ多機能性液体被覆組成物、および使用法 | |
| JP2010013622A (ja) | スプレー剤 | |
| EP0925120B1 (en) | Preparation and method for applying an anti-slip layer to a surface and product provided with an anti-slip layer | |
| US10259928B2 (en) | Silane group-containing polymer composition and coatings containing same | |
| EP1083207A2 (en) | Biocidal coating compositions | |
| JP2826274B2 (ja) | 抗菌性塗料組成物 | |
| WO2009084191A1 (ja) | 徐溶性被膜を有する複合材およびコーティング組成物 | |
| JP2010013621A (ja) | 親水コーティング剤 | |
| CN101193554A (zh) | 抗微生物涂膜 | |
| US5532291A (en) | Coating composition and processes therefor | |
| JP2010013623A (ja) | 水垢付着防止剤 | |
| JP2010275540A (ja) | 漆喰塗布面の艶消し防汚処理材およびそれを用いた防汚仕上げ方法 | |
| HK1015816B (en) | Coatable biocidal compositions | |
| MXPA98000314A (en) | Biocidal compositions that are used to cover a sustr | |
| JP2010013616A (ja) | コーティング組成物 | |
| JPH0889887A (ja) | 抗菌性塗膜の形成方法及びそれによる感染防止方法 | |
| JPS61233602A (ja) | 抗菌性フイルムを形成することができる液体組成物 | |
| JP2995453B2 (ja) | 抗菌性塗料組成物 | |
| BRPI0904137B1 (pt) | artigo tratado na superfície , e, método para fazer tratamento de superfície resistente a bloqueio | |
| JP2001089713A (ja) | 床用処理剤 | |
| JP2004251100A (ja) | 磁器タイル壁面の塗装工法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RENW | Renewal (renewal fees accepted) | ||
| RENW | Renewal (renewal fees accepted) |