NZ739624A - Cleaning composition - Google Patents
Cleaning compositionInfo
- Publication number
- NZ739624A NZ739624A NZ739624A NZ73962418A NZ739624A NZ 739624 A NZ739624 A NZ 739624A NZ 739624 A NZ739624 A NZ 739624A NZ 73962418 A NZ73962418 A NZ 73962418A NZ 739624 A NZ739624 A NZ 739624A
- Authority
- NZ
- New Zealand
- Prior art keywords
- composition
- composition according
- delayed release
- release additive
- surfactant
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 137
- 238000004140 cleaning Methods 0.000 title claims abstract description 43
- 230000003115 biocidal Effects 0.000 claims abstract description 65
- 239000000654 additive Substances 0.000 claims abstract description 42
- 230000003111 delayed Effects 0.000 claims abstract description 42
- 230000000996 additive Effects 0.000 claims abstract description 39
- 239000004753 textile Substances 0.000 claims abstract description 38
- 239000004094 surface-active agent Substances 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 8
- 239000003139 biocide Substances 0.000 claims description 18
- RECUKUPTGUEGMW-UHFFFAOYSA-N Carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- -1 transition metal salt Chemical class 0.000 claims description 7
- 230000000845 anti-microbial Effects 0.000 claims description 6
- 210000004666 bacterial spores Anatomy 0.000 claims description 6
- 239000003613 bile acid Substances 0.000 claims description 6
- 239000000341 volatile oil Substances 0.000 claims description 6
- 235000007746 carvacrol Nutrition 0.000 claims description 5
- RRAFCDWBNXTKKO-UHFFFAOYSA-N Eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims description 4
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims description 4
- 239000005844 Thymol Substances 0.000 claims description 4
- 238000004132 cross linking Methods 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- 229930007823 thymol Natural products 0.000 claims description 4
- 229960000790 thymol Drugs 0.000 claims description 4
- 241000238631 Hexapoda Species 0.000 claims description 3
- MGSRCZKZVOBKFT-UHFFFAOYSA-N Thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 claims description 3
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- 239000012141 concentrate Substances 0.000 claims description 3
- 239000005871 repellent Substances 0.000 claims description 3
- 230000002940 repellent Effects 0.000 claims description 3
- ULDHMXUKGWMISQ-VIFPVBQESA-N (+)-(4S)-carvone Chemical compound CC(=C)[C@H]1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-VIFPVBQESA-N 0.000 claims description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 2
- 229960003767 Alanine Drugs 0.000 claims description 2
- 229940045714 Alkyl sulfonate alkylating agents Drugs 0.000 claims description 2
- 235000005747 Carum carvi Nutrition 0.000 claims description 2
- 240000000467 Carum carvi Species 0.000 claims description 2
- 239000005973 Carvone Substances 0.000 claims description 2
- 235000009024 Ceanothus sanguineus Nutrition 0.000 claims description 2
- 235000005979 Citrus limon Nutrition 0.000 claims description 2
- 240000002268 Citrus limon Species 0.000 claims description 2
- 239000005770 Eugenol Substances 0.000 claims description 2
- 229960002217 Eugenol Drugs 0.000 claims description 2
- 240000006927 Foeniculum vulgare Species 0.000 claims description 2
- 235000004204 Foeniculum vulgare Nutrition 0.000 claims description 2
- QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 claims description 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims description 2
- 229960004873 LEVOMENTHOL Drugs 0.000 claims description 2
- 240000003553 Leptospermum scoparium Species 0.000 claims description 2
- 235000015459 Lycium barbarum Nutrition 0.000 claims description 2
- 240000006217 Mentha pulegium Species 0.000 claims description 2
- 235000016257 Mentha pulegium Nutrition 0.000 claims description 2
- 229940041616 Menthol Drugs 0.000 claims description 2
- 240000005125 Myrtus communis Species 0.000 claims description 2
- 235000013418 Myrtus communis Nutrition 0.000 claims description 2
- 235000016639 Syzygium aromaticum Nutrition 0.000 claims description 2
- 240000005147 Syzygium aromaticum Species 0.000 claims description 2
- WUOACPNHFRMFPN-UHFFFAOYSA-N Terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 claims description 2
- 229940116411 Terpineol Drugs 0.000 claims description 2
- 235000007303 Thymus vulgaris Nutrition 0.000 claims description 2
- 240000002657 Thymus vulgaris Species 0.000 claims description 2
- 239000000642 acaricide Substances 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 2
- 150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
- 239000002280 amphoteric surfactant Substances 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 229930007075 carvone Natural products 0.000 claims description 2
- 229940043350 citral Drugs 0.000 claims description 2
- 229930007907 citral Natural products 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 239000003431 cross linking reagent Substances 0.000 claims description 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecan-1-amine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims description 2
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 claims description 2
- 235000001050 hortel pimenta Nutrition 0.000 claims description 2
- WTEVQBCEXWBHNA-YFHOEESVSA-N neral Chemical compound CC(C)=CCC\C(C)=C/C=O WTEVQBCEXWBHNA-YFHOEESVSA-N 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 235000006678 peppermint Nutrition 0.000 claims description 2
- 235000015132 peppermint Nutrition 0.000 claims description 2
- 235000007735 peppermint Nutrition 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- VQOIVBPFDDLTSX-UHFFFAOYSA-M sodium;3-dodecylbenzenesulfonate Chemical class [Na+].CCCCCCCCCCCCC1=CC=CC(S([O-])(=O)=O)=C1 VQOIVBPFDDLTSX-UHFFFAOYSA-M 0.000 claims description 2
- 150000003505 terpenes Chemical class 0.000 claims description 2
- 235000007586 terpenes Nutrition 0.000 claims description 2
- 239000001585 thymus vulgaris Substances 0.000 claims description 2
- 229910052723 transition metal Inorganic materials 0.000 claims description 2
- 229960004295 valine Drugs 0.000 claims description 2
- 239000004599 antimicrobial Substances 0.000 claims 1
- 239000003093 cationic surfactant Substances 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 238000007865 diluting Methods 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 12
- 210000004215 spores Anatomy 0.000 description 12
- 238000009472 formulation Methods 0.000 description 11
- WVDDGKGOMKODPV-UHFFFAOYSA-N benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 230000000249 desinfective Effects 0.000 description 8
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 7
- SESFRYSPDFLNCH-UHFFFAOYSA-N Benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 4
- 239000004141 Sodium laurylsulphate Substances 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000003809 water extraction Methods 0.000 description 4
- OSDLLIBGSJNGJE-UHFFFAOYSA-N Chloroxylenol Chemical compound CC1=CC(O)=CC(C)=C1Cl OSDLLIBGSJNGJE-UHFFFAOYSA-N 0.000 description 3
- 241000193163 Clostridioides difficile Species 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 235000019445 benzyl alcohol Nutrition 0.000 description 3
- 229960002903 benzyl benzoate Drugs 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 230000000855 fungicidal Effects 0.000 description 3
- 239000000417 fungicide Substances 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000003908 quality control method Methods 0.000 description 3
- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- KYWIYKKSMDLRDC-UHFFFAOYSA-N 2-Undecanone Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 2
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 2
- 241000238876 Acari Species 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 229940100530 ZINC RICINOLEATE Drugs 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 244000052616 bacterial pathogens Species 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229960005443 chloroxylenol Drugs 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 239000000077 insect repellent Substances 0.000 description 2
- 230000000813 microbial Effects 0.000 description 2
- 235000010292 orthophenyl phenol Nutrition 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 230000001603 reducing Effects 0.000 description 2
- 229930000044 secondary metabolites Natural products 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N 2-Phenylphenol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 1
- ZAMOVMHWSVVCQD-UHFFFAOYSA-N 2-benzyl-3-chlorophenol Chemical compound OC1=CC=CC(Cl)=C1CC1=CC=CC=C1 ZAMOVMHWSVVCQD-UHFFFAOYSA-N 0.000 description 1
- 241000239223 Arachnida Species 0.000 description 1
- 229960001230 Asparagine Drugs 0.000 description 1
- 229960000686 Benzalkonium Chloride Drugs 0.000 description 1
- 208000009043 Chemical Burns Diseases 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 229940097362 Cyclodextrins Drugs 0.000 description 1
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 1
- 210000003608 Feces Anatomy 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- DCXYFEDJOCDNAF-UWTATZPHSA-N L-Asparagine Natural products OC(=O)[C@H](N)CC(N)=O DCXYFEDJOCDNAF-UWTATZPHSA-N 0.000 description 1
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N Phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- 229960005323 Phenoxyethanol Drugs 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229940069338 Potassium Sorbate Drugs 0.000 description 1
- CHHHXKFHOYLYRE-STWYSWDKSA-M Potassium sorbate Chemical compound [K+].C\C=C\C=C\C([O-])=O CHHHXKFHOYLYRE-STWYSWDKSA-M 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 229940111630 Tea Tree Oil Drugs 0.000 description 1
- 210000002700 Urine Anatomy 0.000 description 1
- 210000002268 Wool Anatomy 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L Zinc chloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1
- GAWWVVGZMLGEIW-GNNYBVKZSA-L Zinc ricinoleate Chemical compound [Zn+2].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O.CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O GAWWVVGZMLGEIW-GNNYBVKZSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating Effects 0.000 description 1
- ATMLPEJAVWINOF-UHFFFAOYSA-N acrylic acid acrylic acid Chemical compound OC(=O)C=C.OC(=O)C=C ATMLPEJAVWINOF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 230000004059 degradation Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 229960003964 deoxycholic acid Drugs 0.000 description 1
- 230000001419 dependent Effects 0.000 description 1
- 230000001627 detrimental Effects 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000002538 fungal Effects 0.000 description 1
- 230000002209 hydrophobic Effects 0.000 description 1
- 230000001524 infective Effects 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 239000012569 microbial contaminant Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical class C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 230000001264 neutralization Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000004306 orthophenyl phenol Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 235000019477 peppermint oil Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000011528 polyamide (building material) Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000004302 potassium sorbate Substances 0.000 description 1
- 235000010241 potassium sorbate Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002062 proliferating Effects 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 230000001846 repelling Effects 0.000 description 1
- 238000011012 sanitization Methods 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- FHHPUSMSKHSNKW-SMOYURAASA-M sodium deoxycholate Chemical compound [Na+].C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 FHHPUSMSKHSNKW-SMOYURAASA-M 0.000 description 1
- OABYVIYXWMZFFJ-ZUHYDKSRSA-M sodium glycocholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 OABYVIYXWMZFFJ-ZUHYDKSRSA-M 0.000 description 1
- JAJWGJBVLPIOOH-IZYKLYLVSA-M sodium taurocholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCS([O-])(=O)=O)C)[C@@]2(C)[C@@H](O)C1 JAJWGJBVLPIOOH-IZYKLYLVSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002459 sustained Effects 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- 239000010677 tea tree oil Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Abstract
The invention relates to an aqueous cleaning and/or sanitising composition comprising (a) at least one biocidal component (b) a polymeric delayed release additive, and (c) at least one surfactant, wherein said composition dries onto a surface being cleaned to form a dry residue and wherein properties of said dry residue are tailored by manipulation of brittleness of the polymeric delayed release additive through identity and/or quantity of the biocidal component and/or surfactant selected. The composition is intended for the cleaning and/or sanitisation of carpet, upholstery or other textiles. The invention also relates to a method of controlling the friability of the dried residue of the composition. The invention also relates to a method of cleaning and/or sanitising a textile article by applying the composition of the invention to said article, and a process of preparing said cleaning and/or sanitising composition. s of said dry residue are tailored by manipulation of brittleness of the polymeric delayed release additive through identity and/or quantity of the biocidal component and/or surfactant selected. The composition is intended for the cleaning and/or sanitisation of carpet, upholstery or other textiles. The invention also relates to a method of controlling the friability of the dried residue of the composition. The invention also relates to a method of cleaning and/or sanitising a textile article by applying the composition of the invention to said article, and a process of preparing said cleaning and/or sanitising composition.
Description
CLEANING COMPOSITION
Field of the Invention
The invention relates to a composition intended for the cleaning and/or
sanitisation of carpet, upholstery or other textiles.
Background of Invention
Simple effective methods for the routine achievement of effective cleaning
and disinfection of carpets and textile furnishings in domestic dwellings, healthcare
facilities and commercial premises remains a major challenge for chemical
formulators. This is demonstrated by the number of documents issued over the past
several decades each describing attempts to formulate towards this important goal.
The present invention relates to textile disinfectant compositions,
particularly disinfectant compositions for use with carpet, fabric or other textile
surfaces.
The invention has been developed primarily for use as a cleaning and/or
disinfecting composition for heavily soiled and contaminated household, commercial
or institutional fabrics and will be described hereinafter with reference to this
application. However, it will be appreciated that the invention is not limited to this
particular field of use.
Contributing to the difficulties in researching acceptable technologies is the
number of important variables routinely encountered in the market place. The ever-
increasing range of synthetic textiles with specific surface chemistries, presale
chemical treatments, designs, constructions and textures and variations in locations
each contribute to difficulties facing chemical formulators. Types of traffic over textiles
and the chemical and physical properties of soiling matter that will be expected to
accumulate at each separate location, are also major chemical design factors to be
considered.
A particular concern in the care of textiles, such as carpet and other soft
furnishings, besides basic cleanliness, is reducing microbial contaminants to safe
levels (sanitising) as determined by public health requirements. This is especially
important in hospital and other health care facilities where the presence of unwanted
bacteria may be detrimental to the health of recovering patients. Spore forming
organisms pose a particular challenge due to their resistance to most common
disinfection chemicals. The spore-forming organism Clostridium difficile (C. diff) in
particular presents significant issues due to the resilience of the spores and the very
low infective dose required for transmission. In carpeted facilities, such as aged care
homes, disinfecting textiles that have been contaminated with C. diff can be
exceedingly difficult.
The disinfection of heavily soiled and contaminated textiles is difficult for
many reasons. The combination of wetness and organic soil which are commonly
encountered provides an ideal nutrient medium for microbe growth such as algae,
bacterial spores, moulds and other microbes. In addition, if the textile is exposed to
soiling and odours from household animal deposits such as urine or faeces under
conditions of minimal domestic hygiene, disinfection and deodorization present a
major challenge because the deposits are associated with the formation of offensive
odours and microbially active substances which remain in the fabric.
Therefore, the need exists for compositions which are capable of removing
gross organic soiling and also preventing the growth of problematic microorganisms in
carpet and other textiles.
Numerous biocides have been investigated for their potential for
sanitisation of carpets and other soft furnishings such as aldehydes or aldehyde-
releasing chemicals, halogens such as bromine, chlorine and iodine, oxidizing agents
such as hydrogen peroxide, and low molecular weight alcohols such as ethanol and
isopropanol. However, under practical conditions for household fabrics and soft floor
coverings, all have serious practical limitations that restricts use by reasons such as
toxicity and sensitisation (aldehydes), offensive odours (aldehydes, halogens and
oxidising agents), the propensity for causing chemical burns (halogens), potential for
fibre damage and/or dye reduction (oxidizing agents) or flammability (alcohols). These
biocides also have a serious limitation in that they are suitable for the temporary
sanitisation of textiles only and do not impart any residual biocidal activity to the
treated articles.
Others have tried to solve some of these problems with the use of cationic
biocides, however, these are often incompatible with the common stain resist
treatments and also are prone to causing rapid resoiling of carpet if not completely
removed by a subsequent extraction process. Cationic biocides, such as those
described in US Patent Application No. 13/984558, were developed in an attempt to
mitigate some of these issues, but can still exhibit incompatibilities with stain resist
treatments.
While a number of the above materials may provide an appropriate
temporary sanitizing effect, another important concern which these materials do not
address is the presence of dirt-attracting residues, such as residual surfactants from
the cleaning products used. Such residues allow carpet to quickly become unsanitary
because of the soil and bacteria which may be attracted by the residue.
Conventional carpet and upholstery cleaning solutions typically contain
high loadings of non-ionic surfactants intended to solubilise and disperse
contaminates and soil from the surface. Any residual surfactant which is not fully
removed from the fibres during subsequent rinsing remains present on the fibre
surface. The oily nature of these residues causes the fibres to become more sensitive
to re-soiling than fibres which had not been subjected to the cleaning process. These
residues also often lead to undesirable changes in the texture, feel or softness of the
carpet or upholstery surface. Because of the propensity for these residues to lead to
resoiling, it is normal practice to extract said residues from the carpet using hot water
or similar.
Numerous compositions have been described in the art which attempt to
mitigate these issues through the use of surfactants with lower propensity for re-
soiling along with the inclusion of polymers intended to reduce the tackiness of the
dried cleaning solution residue. These compositions, however, do not exhibit the
longevity of biocidal activity necessary for the treatment of heavily soiled areas such
as those that can be found in areas that have been exposed to significant levels of
microbial contamination.
In circumstances with high degrees of microbial contamination, it is highly
desired for a composition capable of generating a residual layer on the textile for an
extended period of time that will prevent the growth of microorganisms. This can be
particularly important in areas where textiles have remained damp for extended
periods. This residual semi-permanent layer can therefore prevent any remaining
organisms from proliferating and also prevent subsequent recolonisation after the
textile is returned to service.
Surprisingly it has been found that through careful selection of biocide,
surfactant and suitable polymeric delayed release additives, it is possible to tailor the
brittleness of the dried residue following application of the present invention to a
textile. Without wishing to be bound by theory, it is thought that the polymeric delayed
release additive is plasticized by the biocide, thus making it less brittle. The
plasticization of the polymeric delayed release additive also serves to slow down the
evaporation of the biocide, thus also controlling its release. In the context of this
invention therefore, the polymeric delayed release additive is functioning as a delayed
release additive. For the purposes of this document the terms "polymeric delayed
release additive" may be regarded as synonymous with the term "delayed release
polymer".
The present invention may be formulated to allow for the biocide to
plasticize the brittle polymeric delayed release additive and therefore generate a
semi-permanent treatment for the textile that will not easily undergo adhesive failure
from the textile fibres. Alternatively, the present invention may be formulated with a
relatively volatile biocide that will plasticize the polymeric delayed release additive but
during the later stages of drying will evaporate from the textile. This will increase the
brittleness of the dried residue and allow it to fracture from the carpet fibres and be
removed by routine cleaning. The present invention allows for the tailoring of the
brittleness of the dried residue to be manipulated depending on the desired
characteristics of the formulation.
Traditional carpet cleaning processes typically involve the use of steam or
hot water extraction steps in order to remove soiling and reduce the level of residual
cleaning compound present on the carpet surface following cleaning. This process
requires the use of bulky and expensive truck mounted extraction machines and also
adds significant levels of moisture to the carpet. This added moisture can contribute
to the growth of microorganisms on the freshly cleaned carpet.
The quantity of water added to the carpet is such that some compositions,
such as those described in US patent application No. 10/904,504, have included
fungicides to prevent the development of fungal growth due to the large quantities of
water applied to the carpet substrate. Hot water extraction is also a time consuming
and labour-intensive method of cleaning. Therefore, it is highly desirable for products
of this nature to have a sufficiently low propensity for resoiling for hot water extraction
to be unnecessary whilst also imparting the semi-permanent antimicrobial layer.
It would be desirable to provide a biocidal composition that imparts a semi-
permanent preventative layer to prevent the regrowth/recolonisation of
microorganisms on the textile surface. It would also be desirable to provide a
composition that does not contribute to the formation of dirt attracting residues and
can also be used without the hot water extraction equipment necessary for traditional
textile cleaning methods.
A reference herein to a patent document or other matter which is given as
prior art is not to be taken as an admission that that document or matter was known
or that the information it contains was part of the common general knowledge as at
the priority date of any of the claims.
Summary of Invention
According to a first embodiment of the present invention there is provided
an aqueous cleaning and/or sanitising composition comprising:
a. at least one biocidal component,
b. a polymeric delayed release additive, and
c. at least one surfactant;
wherein said composition dries onto a surface being cleaned to form a dry residue
and wherein properties of said dry residue are tailored by manipulation of brittleness
of the polymeric delayed release additive through identity and/or quantity of the
biocidal component and/or surfactant selected.
According to a second embodiment of the invention there is provided a
method of controlling friability of dried residue of a cleaning and/or sanitising
composition comprising:
a. at least one biocidal component,
b. a polymeric delayed release additive, and
c. at least one surfactant;
by manipulation of identity and/or quantities of the biocidal component, polymeric
delayed release additive and surfactant.
According to a third embodiment of the invention there is provided a
method of cleaning and/or sanitising a textile article by applying the composition
according to the first embodiment to said article.
According to a fourth embodiment of the invention there is provided a
process of preparing a cleaning and/or sanitising composition by dilution of a
concentrate
a. at least one biocidal component;
b. a polymeric delayed release additive; and
c. at least one surfactant
wherein properties of dried residue of the composition are tailored by manipulation of
brittleness of the polymeric delayed release additive through identity and/or quantity
of the biocidal component and/or surfactant selected.
There is also provided a cleaning and/or sanitising composition according
to the first embodiment capable of generating a semi-permanent antimicrobial
residual layer on treated textiles.
There is also provided a cleaning and/or sanitising composition according
to the first embodiment where the composition is used as a delivery vehicle for
secondary components such as miticides, fungicides, odour absorbing compounds,
animal repellents or insect repellents.
There is also provided a cleaning and/or sanitising composition according
to the first embodiment where the composition includes a spore germinant.
Throughout the description and claims of the specification, the word
"comprises" and variations of the word, such as "comprising" and "comprises", is not
intended to exclude other additives, components, integers or steps.
Detailed Description of the Invention
In accordance with the present invention there is provided an aqueous
cleaning and/or sanitising composition comprising:
a. at least one biocidal component,
b. a polymeric delayed release additive, and;
c. at least one surfactant;
wherein said composition dries onto a surface being cleaned to form a dry residue
and wherein properties of said dry residue are tailored by manipulation of brittleness
of the polymeric delayed release additive through identity and/or quantity of the
biocidal component and/or surfactant selected.
The pH of the compositions generally affects biocidal action, and the
preferred pH will vary depending on the particular biocidal components utilised in the
composition. For example, phenolic biocides are at their most biocidal when present
in their unionised form and a neutral to mild acid pH would be preferable. Phenolic
compounds used in an alkaline medium are also more susceptible to oxidation. For
cationic biocides, a mildly alkaline pH (about 7-9) is preferable due to their increased
biocidal performance in this range.
The selection of pH also generally affects compatibility with the textile type
that is to be treated. For example, for the cleaning of wool, the high level of alkalinity
of woollen blends or silk textiles can cause significant degradation of the textile fibres.
In a more preferred embodiment the pH of the composition is mildly acidic in the
range of about 5.5 to 7.0 to allow for the composition to be used for the cleaning of a
wide range of carpet or upholstery fibres including those which are sensitive to high
levels of alkalinity. Other embodiments may be contemplated that have higher pH
values, for example in the range of about 9 - 11 if their use is only intended for use on
non- alkalinity sensitive fibres such as polyamide or polyolefin.
Biocidal Component
The composition of the invention comprises at least one biocidal
component. In a preferred embodiment, the combination of biocidal components is
stable and maintains its antimicrobial activity during and following the drying of the
composition onto the textile substrate. In a particularly preferred embodiment the
biocidal components may reduce the brittle nature of the polymeric delayed additive,
such that adhesive failure from the textile surface due to the physical forces
experienced during the textile’s normal use, is significantly reduced. In a particularly
preferred embodiment, when used in conjunction with the polymeric delayed release
additive and surfactant, the biocidal components are capable of generating a semi-
permanent antimicrobial prevention layer on treated textiles.
In a preferred embodiment, the biocidal component is selected from the
group consisting of one or more aliphatic or cycloaliphatic terpenes, an aromatic or
phenolic biocide and combinations thereof. In a particularly preferred embodiment the
biocidal component is selected from the non-limiting group consisting of thymol,
carvacrol, eugenol, menthol, terpineol, carvone, citral and combinations thereof. In
another preferred example the biocidal component is a synthetically derived phenolic
compound such as o-phenylphenol, 2-benzylchlorophenol or chloroxylenol.
In a further aspect of the invention the biocidal component may be in the
form of an essential oil such as the essential oils of cloves, thyme, fennel, caraway,
peppermint, lemon myrtle, tea tree or combinations thereof. In a preferred
embodiment, a synergistic combination of thymol and carvacrol are used. In a highly
preferred embodiment, phenolic biocides are used in combination with a biocidal
essential oil.
Alternatively, or in addition, biocidal components that may act as
crosslinking agents may be employed to increase the hardness of the polymeric
delayed release additive to tailor the friability of the dried residue into the desired
range. In a preferred embodiment, the crosslinking biocidal agent is a transition metal
salt. In a particularly preferred embodiment the crosslinking biocidal agent is a zinc
salt.
The total quantity of the biocidal components will be largely dependent on
the antimicrobial activities of the selected components, the degree of soiling of the
textile articles to be treated and if the composition is intended to be diluted prior to
use. Preferably the biocidal components are present in the composition at a
concentration of about 0.01 to 10% w/w of the composition, more preferably at a
concentration of about 0.05 to 5% w/w, even more preferably at a concentration
between about 0.1 to 2% w/w of the composition.
Polymeric delayed release additive
The composition of the invention comprises at least one polymeric delayed
release additive that functions as a polymeric delayed release additive. The least one
polymeric delayed release additive is selected from either a water soluble anionic
acrylic based copolymer or styrene maleic anhydride resin which, on drying, will result
in a non-tacky solid. In a preferred embodiment, the polymeric delayed release
additive will form a brittle film upon drying.
Preferably the polymeric delayed release additives are present in the
composition at a concentration of about 0.5 to 30% w/w of the composition, more
preferably at a concentration of about 1.0 to 15% w/w, even more preferably at a
concentration between about 2 to 10% w/w of the composition.
Preferred examples are the aqueous solutions of acrylic acid/methacrylic
acid copolymers sold under the trade name Syntran 4020, Syntran 4180 and Syntran
4125, all available from Interpolymer Corporation. Another preferred example is
Flexisperse 305 (Innovative Chemical Technologies Inc.). Other polymeric agents will
include styrene maleic anhydride copolymers such as described in US Patent No.
3,835,071.
Typically, within the prior art, these materials find utility as anti-redeposition
polymers. An example of this may be found in US Patent Appl. 13/778,208 (published
as US 2014/0100153) which utilises a styrene maleic anhydride copolymer as an anti-
redeposition agent. As described within the ‘208 teaching, the function of the anti-
redeposition agent is to facilitate sustained suspension of soils in a cleaning solution
and prevent the removed soils from being redeposited onto the substrate being
cleaned.
Surfactant
The composition of the invention includes at least one surfactant.
Preferably the surfactant selected is capable of solubilising the biocidal components
to form a water white, single phase composition. More preferably the surfactant
should be capable of modifying the friability of the polymeric delayed release additive
in conjunction with the biocidal components. Anionic surfactants are preferred due to
foaming characteristics, tackiness of dried residue and compatibility with stain resist
treatments, although embodiments based on non-ionic, cationic and amphoteric are
equally envisioned. In a preferred embodiment, the surfactant is selected from the
group consisting of alkyl sulfates, alkyl ether sulfates, alkyl benzene sulfonates, alkyl
naphthalene sulfonates, alkyl sulfonates, alkyldiphenyloxide disulfonates and
combinations thereof. In a preferred embodiment, the surfactant used is sodium
dodecyl sulfate. In a particularly preferred embodiment, a combination of anionic and
amphoteric surfactants is used.
Preferably the surfactants are present in the composition at a concentration
of about 0.5 to 30% w/w of the composition, more preferably at a concentration of
about 1.0 to 15% w/w, even more preferably at a concentration between about 1.5 to
% w/w of the composition.
Secondary components
In a further aspect of the invention the composition acts as a carrier for
secondary compositions appropriate for the control or management of household
pests, mites or other biological fouling. Embodiments of the invention may also be
suitable for the repellence of insects, arachnids or animals as required. In a preferred
embodiment, the composition of the present invention may serve as a vehicle or
carrier for the transport of secondary compositions appropriate for the control of
household pests, mites etc. These secondary compositions are envisioned to be able
to be carried in the present invention without compromising the biocidal activity of the
present invention.
Examples of such secondary compositions are miticides such as benzyl
alcohol and benzyl benzoate, odour absorbing compounds such as cyclodextrins or
zinc ricinoleate, dog or cat repelling compounds such as 2-undecanone, insect
repellent compounds such as dimethyl phthalate or fungicides such as
phenoxyethanol or potassium sorbate.
In a preferred embodiment, secondary components will be present in the
formulation in an amount between about 0.1 to 5% w/w of the composition of the
invention. In a more preferred embodiment the secondary components will be present
in the formulation in an amount between about 0.1 and 1.0% w/w of the composition.
Bacterial spore germinant
In a further aspect of the invention the composition may also contain a
bacterial spore germinant. The inclusion of a spore germinant causes exposed
bacterial spores to germinate into the vegetative state and therefore be more
susceptible to the action of the biocidal components. Examples of suitable spore
germinants which may be used in the composition of the invention are dodecylamine
and other alkylamines, L-alanine, L-valine, L-asparagine and bile acids.
In a highly preferred embodiment the composition may include the sodium,
potassium or amine salt of a bile acid as a C. difficile spore germinant. In a
particularly preferred embodiment the bile acid spore germinant may be selected from
the group consisting of sodium cholate, sodium taurocholate, sodium glycocholate,
sodium deoxycholate and mixtures thereof.
Given that these bile acids may also function as surfactants, it is envisaged
that some embodiments may only contain these bile acids with no additional
surfactant within the formulation.
In a preferred embodiment, the spore germinant is present in the
formulation in an amount between about 0.001 to 2% w/w of the composition. In a
more preferred embodiment the spore germinant is present in the formulation in an
amount between about 0.005 to 1.0% w/w of the composition.
Examples
The following examples are manufactured by dissolving and mixing the
various ingredients into deionised water at room temperature. Each ingredient is
dissolved to yield a clear solution before the next ingredient is added. A portion of the
water (up to 50%) may be withheld in the initial phase of manufacture and added
when all of the ingredients are dissolved if necessary. More concentrated examples
may require the hydrophobic components to be first solubilised in a surfactant premix
as would be obvious to a person skilled in the art.
Table 1
Weight Percentages of Actives
Ingredient Example 1 Example 2 Example 3 Example 4
SLS 1.5 - - 2.0
2A1 - 1.5 - -
BAK - - 4.0 - - 2.0
PCMX - 0.5 - 2.0
TTO 0.5 - 2.5 1.0
CAR 0.2 - 1.6 -
THY 0.2 - - -
OPP - 0.2 - -
SYN 2.5 - 20.0 -
SMA - 2.5 - 15.0
H O To 100% To 100% To 100% To 100%
LEGEND
SLS – Sodium Lauryl Sulphate
2A1 – Alkyldiphenyloxide Disulfonate
916 – Linear (C9-C11) alcohol ethoxylate 6 mol ethylene oxide
PCMX - Chloroxylenol
PMO – Peppermint Oil
BAK – Benzalkonium Chloride
TTO – Tea Tree Oil
CAR – Carvacrol
THY – Thymol
OPP – ortho-phenylphenol
SYN – Syntran 4125
SMA – Styrene Maleic Anhydride Copolymer
The pH of Examples 1 - 4 may be adjusted with either sodium hydroxide or
citric acid to be within the desired range.
Examples 1 and 2 are intended to be ready-to-use compositions. The
compositions of Examples 3 and 4 may be diluted prior to use. The extent of the
dilution will vary according to the nature and concentration of active ingredient in the
particular formula and the degree of fouling on the particular textile. Dilutions of up to
50 to 1 can be made with the more concentrated products, e.g. Example 3, in
situations where the soiling on the textile is minimal or where the composition is being
applied as a preventative treatment.
More specialised formulations may be prepared from the preceding
formulation to incorporate secondary compounds such as insect/animal repellents,
odour absorbing compounds or miticides. In these cases, the main formulation may
serve as a carrier for the secondary compounds. Examples of these modified
formulations are as follows:
Example 5 - Added miticide
The formulation of Example 1 is modified by the addition of a readily
dispersible solution of miticides, benzyl alcohol and benzyl benzoate.
PREMIX A. 0.5g of benzyl benzoate is mixed with 0.5g benzyl alcohol and
1.5g sodium lauryl sulphate. This is dissolved, if need be, with gentle warming.
2.5g of PREMIX A is added very slowly to 100g of Example 1 under strong
agitation. The resulting solution is mixed for a minimum of 30 minutes at room
temperature. The solution is checked for stability and such other quality control
characteristics as required.
Example 6 - Added odour neutraliser
The formulation of Example 4 is modified by the addition of a readily
dispersible solution of the odour absorbing compound zinc ricinoleate.
PREMIX B. 25.0g of Example 4 is diluted with 100.0g deionised water
while stirring. To this solution is added 5.0g of Tegosorb A30 while stirring. Stirring is
continued for 30 minutes until a clear, homogenous product is obtained. The pH of the
sample is adjusted to the range of 7-9 using sodium hydroxide. The solution is
checked for stability and other quality control characteristics as required.
Example 7 - Included spore germinant
The formulation of Example 2 is modified by the addition of a spore
germinant. In this example, sodium cholate, a germinant for the spores of Clostridium
difficile is used.
0.01g of sodium cholate is added to 100g of Example 2 with stirring under
strong agitation. The resulting solution is mixed for a minimum of 30 minutes at room
temperature. The solution is checked for stability and such other quality control
characteristics as required.
Alternative embodiments
In the following examples, a crosslinking biocide is used to increase the
friability of the dried residue either in isolation or in combination with other biocidal
species. In these embodiments, sodium lauryl sulphate is used as the surfactant and
Syntran 4125 is used as the polymeric delayed release additive.
Table 2
Weight Percentages of Actives
Water 95.5 94
Zinc Chloride 0.5 0.5
Sodium Lauryl Sulphate 1.5 2.5
Carvacrol - 0.5
Syntran 4125 2.5 2.5
Claims (27)
1. An aqueous cleaning and/or sanitising composition comprising: a. at least one biocidal component, b. a polymeric delayed release additive, and c. at least one surfactant; wherein said composition dries onto a surface being cleaned to form a dry residue and wherein properties of said dry residue are tailored by manipulation of brittleness of the polymeric delayed release additive through identity and/or quantity of the biocidal component and/or surfactant selected.
2. A composition according to claim 1, wherein the biocidal component is selected from the group consisting of one or more aliphatic or cycloaliphatic terpenes, an aromatic or phenolic biocide and combinations thereof.
3. A composition according to claim 2, wherein the biocidal component is selected from the group consisting of thymol, carvacrol, eugenol, menthol, terpineol, carvone, citral and combinations thereof.
4. A composition according to any one of claims 1 to 3 also comprising a biocidal essential oil.
5. A composition according to claim 4, wherein the biocidal essential oil is selected from the group consisting of the essential oils of cloves, thyme, fennel, caraway, peppermint, lemon myrtle, tea tree and combinations thereof.
6. A composition according to claim 1, wherein the biocidal component acts as a crosslinking agent of the polymeric delayed release additive.
7. A composition according to claim 6, wherein the crosslinking biocidal component is a transition metal salt.
8. A composition according to any one of claims 1 to 7, wherein the biocide is present at a concentration of between about 0.01 to 10% w/w of the composition.
9. A composition according to claim 8, wherein the biocidal component is present at a concentration of between about 0.1 and 2.0% w/w of the composition.
10. A composition according to any one of claims 1 to 9, wherein the polymeric delayed release additive is selected from a water soluble acrylic polymer/copolymer or styrene-maleic anhydride resin.
11. A composition according to claim 10, wherein the polymeric delayed release additive dries to a friable powder or brittle film.
12. A composition according to any one of claims 1 to 11, wherein the polymeric delayed release additive is present at a concentration of between about 0.5 to 30.0% w/w of the composition.
13. A composition according to claim 12, wherein the polymeric delayed release additive is present at a concentration of between about 2.0 to 10.0% w/w of the composition.
14. A composition according to any one of claims 1 to 13, wherein the surfactants are selected from the group consisting of anionic, cationic, non-ionic and amphoteric surfactants.
15. A composition according to claim 14, wherein the surfactant is selected from the group consisting of alkyl sulfates, alkyl ether sulfates, alkyl benzene sulfonates, alkyl naphthalene sulfonates, alkyl sulfonates, alkyldiphenyloxide disulfonates and combinations thereof.
16. A composition according to any one of claims 1 to 15, wherein the surfactant is present at a concentration of between about 0.5 to 30.0% w/w of the composition.
17. A composition according to claim 16, wherein the surfactant is present at a concentration of about 1.5 to 10.0% w/w of the composition.
18. A composition according to any one of claims 1 to 17, wherein the composition has a pH in the range of about 5.0 to 9.0.
19. A composition according to claim 18, wherein the composition has a pH in the range of about 5.5 to 7.0.
20. A composition according to any one of claims 1 to 19, wherein the composition also contains a bacterial spore germinant.
21. A composition according to claim 20, wherein the bacterial spore germinant is selected from the group consisting of dodecylamine, L-alanine, L-valine, Lasparagine and a bile acid salt.
22. A composition according to any one of claims 1 to 20, wherein the composition also contains an insect/animal repellent, odour absorbing compound or miticide.
23. A composition according to any one of claims 1 to 22 which generates a semi- permanent anti-microbial coating on treated textile articles.
24. A method of controlling friability of dried residue of a cleaning and/or sanitising composition comprising: a. at least one biocidal component, b. a polymeric delayed release additive, and c. at least one surfactant; by manipulation of identity and/or quantities of the biocidal component, polymeric delayed release additive and surfactant.
25. A method of cleaning and/or sanitising a textile article by applying the composition according to any one of claims 1 to 23 to said article.
26. A process of preparing a cleaning and/or sanitising composition, comprising combining: a. at least one biocidal component, b. a polymeric delayed release additive, and c. at least one surfactant; to form a concentrate, wherein properties of dried residue of the composition are tailored by manipulation of brittleness of the polymeric delayed release additive through identity and/or quantity of the biocidal component and/or surfactant selected.
27. A process according to claim 26 comprising diluting said concentrate with water.
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AU2017900319 | 2017-02-02 |
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