GB2324467A - Rapid and long-lasting biocidal system - Google Patents
Rapid and long-lasting biocidal system Download PDFInfo
- Publication number
- GB2324467A GB2324467A GB9708067A GB9708067A GB2324467A GB 2324467 A GB2324467 A GB 2324467A GB 9708067 A GB9708067 A GB 9708067A GB 9708067 A GB9708067 A GB 9708067A GB 2324467 A GB2324467 A GB 2324467A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- salt
- biocide system
- biocide
- ammonium salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
Abstract
A rapidly active and long lasting biocide system for treatment of hard surfaces comprises - at least one water-soluble or water-dispersible monoquaternary ammonium or phosphonium salt biocidal agent or monoquaternary heterocyclic amine salt biocidal agent; and - at least one water-soluble or water-dispersible polymeric quaternary ammonium salt, polymeric quaternary heterocyclic amine salt or polymeric cationic biguanide salt.
Description
RAPID AND LONG LASTING BIOCIDAL SYSTEM AND ITS USE TO THE
TREATMENT OF HARD SURFACES
The invention relates to a rapid and long lasting biocide system, to its use in biocidal aqueous compositions, particularly for the biocidal treatment of hard surfaces, and to a method for rapid and long lasting biocidal treatment of hard surfaces.
Monoquaternary ammonium or phosphonium salt biocides and monoquaternary heterocyclic amine salt biocides are known as having rapid activity particularly when applied on hard surfaces, but they suffer from the disadvantage of having to be used in relatively high amounts.
It has been proposed, in order to control biocide release, to provide a liquid biocidal composition containing the biocide and a film forming polymer or copolymer such as polyvinylpyrrolidone, copolymers of vinylpyrrolidone and vinyl acetate, copolymers of vinyl ethers and maleic anhydride (GB-A-1 553 132), acrylic or methacrylic copolymers (EP-A-O 290 676) or terephthalic copolyesters (WO 97/06675). The polymer or copolymer film formed on the hard surface holds and protects the biocide, which is slowly released to give extended disinfectancy, by resistance to washing.
Such compositions suffer the disadvantage that they contain a relatively high concentration of polymer compared to the concentration of biocide; besides the increase in cost, this prevents the provision of rapid disinfection.
Further it may also create problems in formulation because most of these polymers are insoluble in water, and thus difficult to formulate in aqueous products.
Thus, a need exists for a biocidal product and a biocidal composition capable of being both rapid acting and long lasting and which can be used at low level.
According to the present invention, there is provided a biocidal system which is able to provide both in-built rapid acting disinfection (for example as little as 5 minutes after having been applied to a hard surface) and in-built extended disinfectancy (for example 24 hours, indeed 3 days or more after having been applied to said hard surface). This biocidal system is composed of a combination of a monocationic salt biocidal agent and a polymeric cat ironic salt compound; isobolograms show that the agent and compound mutually support each other very significantly in their effects and that a lower concentration of biocide is required to achieve the same effect; impact on the environment is thus reduced.
Further, said biocidal system is easy to formulate, particularly in non-ionic active cleaners.
According to the present invention, there is provided a rapidly active and long lasting biocide system (BS) comprising
- at least one watersoluble or waterdispersible monoquaternary ammonium or phosphonium salt biocidal agent or monoquaternary heterocyclic amine salt biocidal agent (M); and
- at least one watersoluble or waterdispersible polymeric quaternary ammonium salt, polymeric quaternary heterocyclic amine salt or polymeric cat ironic biguanide salt (P) (BS) is generally is in the form of an aqueous solution. Preferably at least one non-ionic, amphoteric or zwitterionic surfactant is present.
The present invention also provides the use in a biocidal aqueous composition (BAC), of a biocide system (BS) as defined above as well as a method for the biocidal treatment of a hard surface which comprises applying to said surface a biocidal aqueous composition (BAC) as defined above.
The (BAC) is preferably a hard surface treatment or cleaning composition.
Suitable biocidal agents include: -mono- or -di-(higher alkyl) quaternary ammonium salts such as
N-higher alkyl-N-aryl-N,N-di(lower alkyl) ammonium salts such as R1R2R3R4N+X where
R1 is optionally chloro substituted benzyl, or Cl-C4 alkyl benzyl,
R2 is C8-C24 alkyl,
R3 and R4 are each independently Cl-C4 alkyl or Cl-C4 hydroxyalkyl, and X is a water solubilising anion such halide (e.g.
chloride, bromide, iodide), sulfate, or methylsulfate.
Generally "lower alkyl" as used herein, means alkyl of 1 to 4 carbon atoms while "higher alkyl" means alkyl of at least 8 carbon atoms.
Specific examples include coco-alkyl benzyl dimethylammonium chloride, C12 - C14 alkyl benzyl dimethyl ammonium chloride, coco-alkyl dichlorobenzyl dimethylammonium chloride and tetradecyl benzyl dimethylammonium chloride.
*N, N-di (higher alkyl)-N,N-di(lower alkyl) ammonium salt such as Rl'R2'R3R4N+X- where
R' and R' are each independently, C8-C24 alkyl,
R3 and R4 are each independently, Cl-C4 alkyl, and X is a water solubilising anion such as defined above, such as dodecyl dimethylammonium chloride and dioctyl dimethylammonium chloride.
*N-higher alkyl-N,N,N-tri(lower alkyl) ammonium salts such as
R"R''R "R4"N+X- where
R" is C8-C24 alkyl
R", R " and R4" are each independently Cl-C4 alkyl, and X is a water solubilizing anion such as defined above such as myristyl trimethylammonium bromide and cetyl trimethylammonium bromide.
- monoquaternary heterocyclic amine salts such as laurylpyridinium chloride, cetylpyridinium chloride, C12- C14-alkyl-benzyl imidazolinium chloride.
- higher alkyl triphenyl phosphonium salts wherein the anion is generally a water solubilising anion as defined for X, such as -myristyl triphenyl phosphonium bromide.
Preferably (P) is water soluble and is a biocide such as: - polymers from the reaction of *epichlorhydrin and dimethylamine or diethylamine e.g. poly[hydroxyethylene(dimethylamino)-2hydroxypropyl(dimethylamino)methylene dichloride]; *epichlorhydrin and imidazole; *1,3-dichloro-2-propanol and dimethylamine; *1,3-dichloro-2-propanol and l,3-bis-dimethylamino-2- propanol; *ethylene dichloride and 1,3-bis-dimethylamino-2-propanol; *bis(2-chloroethyl)ether and N,N,N',N'-tetramethylethylene diamine that is polyoxyethylene (dimethylamino) ethylene (dimethylamino) dichloride; *bis(2-chloroethyl)ether and N,N'-bis(dimethylaminopropyl) urea or thiourea; *polymeric biguanidine hydrochloride such as VANTOCIL IB (ICI).
These (P) polymers generally have a molecular weight from 500 to 1,000,000 preferably from 1,000 to 40,000.
The weight ratio (dry basis) (M)/(P) in (BS) is generally from 10/90 to 90/10, preferably 15/85 to 80/20, particularly 20/80 - 40/60 and especially about 25/75.
(BS) is preferably in the form of an aqueous concentrate containing up to, say, 50%, preferably up to 30 or 40%, by weight of (M) + (P) (dry basis). It can be prepared by simply mixing solutions of (M) and (P). Thus, typically, the concentrate will contain 1 to 20%, especially 1 to 10% by weight of (M) and 3 to 60%, especially 3 to 30%, by weight of (P) (as active materials).
(BS) can be used as a rapid and long lasting biocide agent (additive) in a biocidal aqueous composition (BAC).
(BS) and/or (BAC) can contain at least one non-ionic, amphoteric or zwitterionic surfactant. Typically the concentration of surfactant corresponds to the weight ratio (dry basis) of surfactant/(BS) of 0.2/1 to 8/1 preferably 1/1 to 5/1.
Examples of suitable non-ionic surfactants include block polymers of ethylene oxide and propylene oxide, polyethoxylated sorbitan esters, sorbitan fatty esters, ethoxylated fatty esters (e.g. 1-25 oxyethylene units), ethoxylated C8-C22 alcohols (e.g. 1-12 oxyethylene units), polyethoxylated C6-C12 alkylphenols (e.g. 5-25 oxyethylene units), alkylpolyglycosides, amine oxides (such as C10-Cl8 alkyldimethylamineoxides, C8-C22 alkoxyethyl dihydroxyethylamineoxides).
Examples of suitable amphoteric or zwitterionic surfactants include
C6-C20 alkylamphoacetates or alkylamphodiacetates (such as cocoamphoacetates), C10-Cl8 alkyldimethylbetaines, C10-Cl8 alkylamidopropyldimethylbetaines, C10-Cl8 alkyldimethyl sulphobetaines, C10-Cl8 alkylamidopropyldimethyl sulphobetaines.
In a preferred embodiment, (BAC) is an aqueous hard surface treatment or cleaning composition.
Other possible ingredients of the composition include: * chelating agents such as aminocarboxylates (ethylenediaminetetraacetates, nitrilotriacetates, N,Nbis(carboxymethyl) glutamates), citrates; * builders such as phosphates, silicates; * alcohols such as ethanol, isopropanol, glycols; * Perfumes and colorants.
The (BAC) compositions can be prepared simply by dilution of (BS) in water.
When other additives are present in (BAC) compositions, said additives can be added either to the (BS) system or to the dilution water or to the diluted formulation, said additives are preferably introduced in (BS) when (BS) is a solution.
Examples of microorganisms which can be controlled include: (i) Gram negative bacteria: Pseudomonas aeruginosa;
Escherichia coli; and Proteus mirabilis.
(ii) Gram positive bacteria: Stahvlococcus aureus; and
Streptococcus faecium.
(iii) Other harmful food bacteria: Salmonella tvPhimurium; Listeria monocytogenes; CamPylobacter iefuni; and Yersinia enterocolitica.
(iv) Yeasts: Saccharomvces cerevisiae; and Candida albicans.
(v) Fungi: AsPerqillus niter; Fusarium solani; and
Pencillium chrvsosenum.
(vi) Algae: Chlorella saccharophilia; Chlorella emersonii;
Chlorella vulsaris; and Chiamydomonas eusametos.
The microorganisms controlled by the method of the present invention are preferably Gram negative microorganisms, especially Pseudomonas aerusinosa, Gram positive microorganisms, especially StaPhylococcus aureus, and fungi e.g. Asrergillus niger.
The (BAC) compositions may be applied to the hard surface by coating, spraying, dipping, brushing or wiping, for example. It can be used as surface disinfectant for floors, walls, working surfaces, equipment, furniture, instruments, in hospitals, food plants, breweries and the home (e.g. kitchens and bathrooms). Examples of hard surfaces which can be treated include glazed or unglazed ceramics, glass, PVC, plastic laminate and other hard plastics, stainless steel or other painted or unpainted metals and painted or unpainted wood as well as flexible polymer surfaces.
The amount used will, of course, depend to some extent on the nature of the surface but, generally, total actives should amount to 1 to 1000 ppm, preferably 5 to 500 ppm.
The following Examples further illustrate the present invention.
Test protocol for evaluation of (M)/(P) biocide system (BS) for biocidal activity according to AFNOR 72.150 Standard
Test
Conditions *biocide dilutions : prepared in distilled water *test organism : Pseudomonas aeruginosa ATCC
15442 *temperature : 200C *contact time : 5 minutes and extended to 24
hours *organic matter : Nil *inactivator solution : 3% Tween 80 + 2% Soya
Lecithin *result : dilution to give 5 log
reduction, i.e. 99.999% kill
Procedure 1. Prepare serial dilutions of (M)/(P) biocidal system (BS) with different ratios (M)/(P); 2. inoculate said test dilutions with Pseudomonas aeruginosa bacterial suspension; 3. sample after 5 minutes and 24 hours, by transferring lml of test dilution to 9 mls of inactivator solution; 4. plate out inactivated test dilution on nutrient agar, incubate at 370C for 48 hours and assess for bacterial survivors; 5. calculate dilution which gives 5 log reduction in bacterial numbers.
When all the results had been collated, the t Fractional
Bacterial Concentration ( FBC) was calculated for each particular blend.
The Fractional Bacterial Concentrations (FBC) method compares the biocidal effect of each biocide compound when used in the biocide mixture to the effect produced when each biocide compound is used alone.
FBC = concentration in the mixture/concentration
when used alone E FBC = FBC (M) + FBC (P) E FBC = 1 corresponds to a normal additive effect E FBC = > 1.0 corresponds to antagonism E FBC = < 1.0 corresponds to synergy
Example 1
The tested biocide system (BS) consists of a blend of
- RHODAQUAT RP 50 (Rhone-Poulenc), an aqueous solution containing 50% solids of C12-Cl4 alkyl benzyl dimethyl ammonium chloride;
- and GLOKILL PQ (Rhone-Poulenc), an aqueous solution containing 50% solids of a polymer from epichlorhydrin and dimethylamine.
The five following dilutions were prepared
RHODAQUAT RP50 10% 7.5t 5.0t 2.5 0% ppm active 50,000 37,500 25,000 12,500 GLOKILL PQ 0% 2.5t 5.0* 7.5 10% ppm active 12,500 25,000 37,500 50,000 water to 100t to 100% to 100% to 100t to 100% 5 minutes test results
RP50 PQ Biocidal actives in ppm FBC FBC EFBC dilution RP 50 PQ RP50 PQ 10% 0% 1 : 1000 50 0 5% 5% 1 : 750 33.33 33.33 0.66 0.33 1 0% 10% 1 : 500 0 100 24 hours test results
RP50 PQ Biocidal actives in ppm FBC FBC #FBC dilution RP 50 PQ RP50 PQ 10% 0% 1 : 2000 25 0 7.5t 2.56 1 : 3500 10.71 3.57 0.428 0.286 0.714 5% 5% 1 : 4000 6.25 6.25 0.250 0.500 0.750 2.56 7.5 1 : 5500 2.27 6.82 0.091 0.546 0.637 0% 10% 1 : 4000 0 12.5 An additive effect can be noted after 5 minutes (but no antagonism) and a significant synergy after 24 hours, particularly for the ratio RP50 / PQ of 1/3.
Example 2
Example 1 is repeated replacing GLOKILL PQ by GLOKILL ELC (Rhone-Poulenc), an aqueous solution containing 50% solids of a polymer from epichlorphydrin and imidazole.
24 hours test results
RP50 ELC Biocidal actives in ppm FBC FBC CFBC dilution I RP 50 ELC RP50 ELC 10% 0% 1 : 2000 25 0 7.58 2.5% 1 : 4000 9.37 3.125 0.375 0.375 0.750 5% 5% 1 : 5000 5.00 5.00 0.200 0.600 0.800 2.58 7.56 1 : 6000 2.08 6.25 0.083 0.750 0.833 0% 10% 1 : 6000 0 8.33 Synergy after 24 hours can be noted here too.
Claims (13)
1. A rapidly active and long lasting biocide system (BS) comprising
- at least one watersoluble or waterdispersible monoquaternary ammonium or phosphonium salt biocidal agent or monoquaternary heterocyclic amine salt biocidal agent (M); and
- at least one watersoluble or waterdispersible polymeric quaternary ammonium salt, polymeric quaternary heterocyclic amine salt or polymeric cat ironic biguanide salt (P).
2. A biocide system according to claim 1 in the form of an aqueous solution.
3. A biocide system according to claim 1 or 2 comprising at least one non-ionic, amphoteric or zwitterionic surfactant.
4. A biocide system according to any one of the preceding claims wherein the biocidal agent is a -mono- or -di-(higher alkyl) quaternary ammonium salt.
5. A biocide system according to any one of the preceding claims wherein the biocidal agent is a N-higher alkyl-N-aryl-N,N-di(lower alkyl) ammonium salt, a N,Ndi(higher alkyl)-N,N-di(lower alkyl) ammonium salt, a Nhigher alkyl-N,N,N-tri(lower alkyl) ammonium salt, a monoquaternary heterocyclic amine salt or a higher alkyl triphenyl phosphonium salt.
6. A biocide system according to claim 5 wherein the N-higher alkyl-N-aryl-N,N-di(lower alkyl) ammonium salt is RlR2R3R4N+X- where
R1 is optionally chloro substituted benzyl, or Cl-C4 alkyl benzyl, R2 is C8-C24 alkyl,
R3 and R4 are each independently C1-C4 alkyl or C1-C4 hydroxyalkyl, and X is sulfate, or methylsulfate; or the N,N-di(higher alkyl)-N,N-di(lower alkyl) ammonium salt is
R'R'R 'R4'N+X- where
R' and R2 are each independently, C8-C24 alkyl, R3' and R4' are each independently, C1-C4 alkyl, and X is halide, sulfate or methylsulfate; or the N-higher alkyl-N,N,N-tri(lower alkyl) ammonium salt is R1 R2 R3 R4 N+X- where
R" is C8-C24 alkyl R2", R " and R4" are each independently C1-C4 alkyl, and X- is halide, sulfate or methylsulfate; or the monoquaternary heterocyclic amine salt is laurylpyridinium chloride, cetylpyridinium chloride, C12
C14-alkyl-benzyl imidazolinium chloride; or the higher alkyl triphenyl phosphonium salt is myristyl triphenyl phosphonium bromide.
7. A biocide system according to any one of the preceding claims wherein the weight ratio (dry basis) (M)/(P) is 15/85 to 80/20.
8. A biocide system according to claim 7 wherein the weight ratio (dry basis) (M)/(P) is 25/75.
9. A biocide system according to any of the preceding claims, in the form of an aqueous concentrate, comprising up to 50% by weight of (M) + (P) (dry basis).
10. A biocide system according to claim 9 comprising 5 to 10% by weight (dry basis) of (M) and 15 to 30% by weight (dry basis) of P.
11. A biocide system according to claim 1 substantially as hereinbefore described.
12. A process for the biocidal treatment of a hard surface which process comprises applying to said surface a biocide system according to any one of the preceding claims.
13. A process according to claim 12 substantially as hereinbefore described.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9708067A GB2324467A (en) | 1997-04-22 | 1997-04-22 | Rapid and long-lasting biocidal system |
AU70669/98A AU7066998A (en) | 1997-04-22 | 1998-04-22 | Rapid and long lasting biocidal system |
PCT/GB1998/001176 WO1998047359A1 (en) | 1997-04-22 | 1998-04-22 | Rapid and long lasting biocidal system |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9708067A GB2324467A (en) | 1997-04-22 | 1997-04-22 | Rapid and long-lasting biocidal system |
Publications (2)
Publication Number | Publication Date |
---|---|
GB9708067D0 GB9708067D0 (en) | 1997-06-11 |
GB2324467A true GB2324467A (en) | 1998-10-28 |
Family
ID=10811122
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9708067A Withdrawn GB2324467A (en) | 1997-04-22 | 1997-04-22 | Rapid and long-lasting biocidal system |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU7066998A (en) |
GB (1) | GB2324467A (en) |
WO (1) | WO1998047359A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102006051559A1 (en) * | 2006-11-02 | 2008-05-08 | Merz Pharma Gmbh & Co. Kgaa | Cleaning- and disinfectant- concentrate, useful in hygienic surfaces and medical area, preferably medical instruments and composite materials, comprises water, cationic biocidal active agents, amines and heterocyclic components |
DE102006051560A1 (en) * | 2006-11-02 | 2008-05-08 | Merz Pharma Gmbh & Co. Kgaa | Cleaning- and disinfecting-concentrate, useful in hygienic surfaces, medical area preferably medical instruments and composite materials, comprises water, cationic biocidal active agents, amines, heterocyclic components and surfactants |
US9750258B2 (en) | 2013-10-14 | 2017-09-05 | Lonza Inc. | Stable composition for controlling biological growth and method for using same in oil field applications |
WO2022048986A1 (en) * | 2020-09-02 | 2022-03-10 | Jointinventions Gmbh | Surface-active disinfectant |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU1180300A (en) * | 1998-11-16 | 2000-06-05 | Rohto Pharmaceutical Co., Ltd. | Liquid ophthalmic preparations |
US6303557B1 (en) | 1999-11-16 | 2001-10-16 | S. C. Johnson Commercial Markets, Inc. | Fast acting disinfectant and cleaner containing a polymeric biguanide |
US8431751B1 (en) | 2008-12-24 | 2013-04-30 | Alcon Research, Ltd. | Polymeric quaternary ammonium compounds with vicinal hydroxy groups |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0099209A1 (en) * | 1982-07-01 | 1984-01-25 | JOHNSON & JOHNSON MEDICAL, INC. | Aqueous disinfectant solutions having residual biocidal activity |
US5049383A (en) * | 1987-04-07 | 1991-09-17 | Hoechst Ag | Aqueous biocidal cationic dispersions of polymers and their use as fungicidal, bactericidal and algicidal treatment agents |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2483177A1 (en) * | 1980-05-29 | 1981-12-04 | Salkin Nicolas | NOVEL DISINFECTANT COMPOSITION COMPRISING A QUATERNARY AMMONIUM AND A HEXAMETHYLENE BIGUANIDE HYDROCHLORIDE OLIGOMER |
DE3445901A1 (en) * | 1984-12-15 | 1986-06-19 | Henkel KGaA, 4000 Düsseldorf | LIQUID DISINFECTANT PREPARATIONS WITH BROADBAND EFFECT |
GB8625103D0 (en) * | 1986-10-20 | 1986-11-26 | Unilever Plc | Disinfectant compositions |
BE1003510A5 (en) * | 1989-10-09 | 1992-04-07 | Fabricom Air Conditioning Sa | DISINFECTANT COMPOSITION AND DISINFECTION METHOD. |
FR2662174B1 (en) * | 1990-05-15 | 1993-10-15 | Eparco | CLEANING AND DISINFECTION COMPOSITIONS FOR HOUSEHOLD USE WITH HYPOALLERGENIC PROPERTIES AND ARACID CAPACITIES. |
FR2695297B1 (en) * | 1992-09-08 | 2000-11-03 | Disinfectant agent composition. |
-
1997
- 1997-04-22 GB GB9708067A patent/GB2324467A/en not_active Withdrawn
-
1998
- 1998-04-22 WO PCT/GB1998/001176 patent/WO1998047359A1/en active Application Filing
- 1998-04-22 AU AU70669/98A patent/AU7066998A/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0099209A1 (en) * | 1982-07-01 | 1984-01-25 | JOHNSON & JOHNSON MEDICAL, INC. | Aqueous disinfectant solutions having residual biocidal activity |
US5049383A (en) * | 1987-04-07 | 1991-09-17 | Hoechst Ag | Aqueous biocidal cationic dispersions of polymers and their use as fungicidal, bactericidal and algicidal treatment agents |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102006051559A1 (en) * | 2006-11-02 | 2008-05-08 | Merz Pharma Gmbh & Co. Kgaa | Cleaning- and disinfectant- concentrate, useful in hygienic surfaces and medical area, preferably medical instruments and composite materials, comprises water, cationic biocidal active agents, amines and heterocyclic components |
DE102006051560A1 (en) * | 2006-11-02 | 2008-05-08 | Merz Pharma Gmbh & Co. Kgaa | Cleaning- and disinfecting-concentrate, useful in hygienic surfaces, medical area preferably medical instruments and composite materials, comprises water, cationic biocidal active agents, amines, heterocyclic components and surfactants |
US9750258B2 (en) | 2013-10-14 | 2017-09-05 | Lonza Inc. | Stable composition for controlling biological growth and method for using same in oil field applications |
WO2022048986A1 (en) * | 2020-09-02 | 2022-03-10 | Jointinventions Gmbh | Surface-active disinfectant |
Also Published As
Publication number | Publication date |
---|---|
WO1998047359A1 (en) | 1998-10-29 |
AU7066998A (en) | 1998-11-13 |
GB9708067D0 (en) | 1997-06-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6303557B1 (en) | Fast acting disinfectant and cleaner containing a polymeric biguanide | |
JP5615708B2 (en) | Formulation containing antimicrobial composition | |
JP6076374B2 (en) | Antimicrobial composition | |
CN109561694B (en) | Antimicrobial compositions | |
EP2046936A2 (en) | Biocidal compositions and methods | |
WO2013061082A1 (en) | Anti-microbial composition | |
WO2005044966A1 (en) | Cleaning compositions | |
AU716919B2 (en) | Cleaning and/or disinfecting composition | |
CN103562368A (en) | Broad spectrum disinfectant | |
EP2539424B1 (en) | Toilet bowl cleaner and method | |
CN104202973A (en) | Anti-microbial compositions and related methods | |
US6762162B1 (en) | Disinfecting cationic polymer cleaner comprising an acrylate cationic polymer | |
KR20200130486A (en) | Composition and method for long lasting disinfection | |
GB2324467A (en) | Rapid and long-lasting biocidal system | |
JP2019006832A (en) | Antimicrobial composition | |
US6465409B1 (en) | System based on a biocide and on a polyether silicon for disinfecting hard surfaces | |
WO2011015881A2 (en) | Biocidal composition | |
WO2023275536A1 (en) | Laundry sanitizing composition | |
GB2433510A (en) | A composition for use in the treatment of a surface. | |
US20240108000A1 (en) | Disinfectant compositions exhibiting enhanced biocidal benefits | |
WO2014060755A1 (en) | Cleaning, sanitizing and sterilizing preparations | |
EP4112706A1 (en) | Laundry sanitizing composition | |
JP2023021253A (en) | antimicrobial composition | |
CN116438285A (en) | Aqueous cleaning composition comprising nonionic surfactant, quaternary ammonium compound and chelating agent | |
WO2005011377A1 (en) | A composition for use in the treatment of a surface |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |