GB1571517A - Deodorizing composition and method - Google Patents
Deodorizing composition and method Download PDFInfo
- Publication number
- GB1571517A GB1571517A GB48187/76A GB4818776A GB1571517A GB 1571517 A GB1571517 A GB 1571517A GB 48187/76 A GB48187/76 A GB 48187/76A GB 4818776 A GB4818776 A GB 4818776A GB 1571517 A GB1571517 A GB 1571517A
- Authority
- GB
- United Kingdom
- Prior art keywords
- parts
- pvp
- composition
- polyvinyl pyrrolidone
- weight
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 41
- 238000000034 method Methods 0.000 title claims description 24
- 230000001877 deodorizing effect Effects 0.000 title claims description 11
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims abstract description 55
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims abstract description 55
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims abstract description 54
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- 239000012141 concentrate Substances 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 229940042935 dichlorodifluoromethane Drugs 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229940043237 diethanolamine Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229960002737 fructose Drugs 0.000 description 1
- 235000004611 garlic Nutrition 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 208000007565 gingivitis Diseases 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940046892 lead acetate Drugs 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(ii) nitrate Chemical compound [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 230000008447 perception Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000021108 sauerkraut Nutrition 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 208000003265 stomatitis Diseases 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 239000002023 wood Substances 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
- 229940100530 zinc ricinoleate Drugs 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/817—Compositions of 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 a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
- A61K8/8176—Homopolymers of N-vinyl-pyrrolidones. Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Abstract
The composition contains a) polyvinylpyrrolidone as odour-binding component and b) at least one vehicle. Component b) can be water and/or alcohol or a pharmaceutical and/or cosmetic vehicle. The composition can be used in deodorising products.
Description
(54) DEODORIZING COMPOSITION AND METHOD
(71) I, RUDOLF KÜRNER, a citizen of the Federal Republic of Germany, of
Wehrheimer Strasse 1, D-6380 Bad Hom- burg v.d.H. Federal Republic of Germany, do hereby declare the invention for which I pray that a patent may be granted to me, and the method by which it is to be performed to be particularly described in and by the following statement:
This invention relates to a method for deodorizing. Up to now, offensive odours have been modified or covered by addition of pleasantly smelling substances. This applies to technical fields as well as to cosmetics and hygienics. Thus, a diluting and covering effect. respectively, was achieved.
Another possibility for reducing unpleasant odours lies in the use of filmforming materials such as zinc ricinoleate or copolymers of polyvinyl pyrrolidone and vinyl acetate, which apparently fix the odour molecules by encasing fine suspended particles. However, when film-forming materials are added to scented smellcovering agents, the substrates are prevented from releasing scent molecules since they are now coated with non-evaporating films. Even desirable odours are, thus, suppressed or dampened. This so-called "cheese-plate cover" effect makes it impossible to use such compositions for arm-pits, feet and the like since it is generally known that the plugging of sweat pores may result in serious irritations of the skin. Furthermore. the stickiness of these compositions is unfavourable in a physiological sense.
Antiseptic agents are used to prevent bacterial decomposition of sweat and the development of body odours in arm-pits, on feet and the like. In this way, disagreeable odours are stopped before they may start.
Only lauryl methacrylate is considered a true smell-destroying compound; it acts by generating less odorous copolymers. A chemical effect is utilized here to destroy odours. The chemical nature of the compound and the fact that it is normally manufactured as 80% concentrate in hydrocarbons does, however, not permit its use on humans.
All previous attempts to explain the mechanisms and effects of so-called "smelldestroyers" have involved tests in the gaseous phase in order to simulate the phenomena accompanying the perception of smells as closely as possible.
Former tests (see H.P. Fiedler, "Der
Schweiss", Editio Cantor, Aulendorf, 18.
Beiheft der Arzneimittelforschung, 1968, page 494) have shown, for instance, that essentail oils and active substances in smelldestroying compositions primarily occupy the olfactory cells of the human nose leaving no room for "stink molecules".
All known smell-destroying agents have the disadvantage of showing no selectivities for offensive odours.
German patent 899 248 describes the use of polyvinyl pyrrolidone in preparing socalled dry perfumes. The perfume oil may be added in "dry form" to powdery compositions such as bath-salts; it is completely soluble in the bathing-water and unfolds its scent freely. Compositions of this nature which release fragrant substances to the surroundings, will, however, not remove odours.
Surprisingly, it has now been found that polyvinyl pyrrolidone soluble in water and alcohol acts as true smell-removing agent.
The term "soluble in alcohol" means that the compound can be dissolved in lower aliphatic alcohols having up to 3 carbon atoms.
Suitable are polyvinyl pyrrolidones soluble in water and alcohol which have a k-value of about 5 to 150, preferably about 10 to 95 and especially preferred of about 25-75, particularly about 30 to about 60 the k-value may be defined by the following equation:
k =t (log n rel)/c in which n is the viscosity of the solution in relation to the solvent and c is the concentration in grams per 100 milliliters of solution.
The above mentioned types of polyvinyl pyrrolidone generally have an average molecule weight of about 5000 to 2 000 000; preferred are compounds having an average molecular weight of about 10 000 to 1 000 000 and especially of about 13 000 to 450 000.
The polymeric polyvinyl pyrrolidone soluble in water and alcohol is employed in solutions or admixed with known pharmaceutical, cosmetic or technical carriers or synthetic materials.
Suitable solvents are water and mono- or polyvalent alcohols having up to 6 carbon atoms, preferably water and/or mono- or polyvalent aliphatic alcohols having 1 to 3 carbon atoms; if desired, di- to hexavalent alcohols having up to 6 carbon atoms may be added in amounts up to 50% by weight, preferably up to 30% by weight and especially up to 10% by weight. The following solvents may also be used: alcohols such as methanol, ethanol, propanol, isopropanol, butanol. sec. butanol, amyl alcohol, 2-ethyl1-hexanol, cyclohexanol, phenol (50"C), ethylene glycol, propylene glycol, 1,3butane diol, 1,4-butane diol, glycerol; ketone alcohols such as diacetone alcohol; aliphatic carboxylic acids such as formic acid, acetic acid, propionic acid; etheralcohols such as "Solvofen" glycol ether (GAF), diethylene glycol, triethylene glycol. hexamethylene glycol, polyethylene glycol 400; 2,2'- thio diethanol; lactones such as butyrolactone; ester such as ethyl acetat; ketones such as methyl cylcohexanone; chlorinated hydrocarbons such as methylene dichloride, chloroform, ethylene dichloride; dichloro monofluoro methane, chloro difluoro methane; lactames such as 2-pyrrolidone, N-methyl-2-pyrrolidone, N Vinyl-2-pyrrolidone; amines such as butyl amine, cyclohexyl amine, aniline, ethylene diamine, pyridine. morpholine, 2-amino ethanol, diethanol amine, triethanol amine, aminoethylethanol amine, 2-hydroxyethyl morpholine, 2-amino-2-methyl- 1-propanol; nitro paraffines such as nitro methane, nitro ethane.
Together with lower aliphatic alcohols having 1 to 4 carbon atoms and preferably 2 to 3 carbon atoms, the following hydrocarbon halides may be used: trichloro fluoro methane, dichloro difluoro methane, 1,1,2 trichloro-1 ,2,2-trifluoro ethane, 1,2dichloro-1,1,2,2-tetrafluoro ethane, 1 chloro-l, 1-difluoro ethane. The mixing ratio of hydrocarbon to alcohol generally lies between 90/10 and 60/40 parts by weight, preferably between 80/20 and 70/30 parts by weight.
Preferably, 0.1-75 parts by weight of PVP are dissolved in 99.9 - 25 parts by weight of solvent. Typically, the concentration of polyvinyl pyrrolidone in the solution amounts to about 01% by weight, preferably 0.2 to 10% by weight and especially to 0.3 to 3.0% by weight, based upon the total weight of the solution.
Suitable carriers are water-soluble, waterinsoluble and water-swellable carriers.
Water-soluble carriers are, for instance: water-soluble sugars such as dextrose, lactose, levulose, cane and beet sugar, respectively;
sugar alchols such as sorbite;
inorganic or organic salts such as aluminum potassium sulfate, aluminum sulfate, ammonium chloride, ammonium sulfate, barium chloride, calcium chloride, chromium sulfate, copper sulfate, iron sulfate, magnesium chloride, mercury acetate, nickel nitrate, lead acetate, potassium chloride, potassium sulfate, potassium dichromate, sodium bicarbonate, sodium chloride, sodium nitrate, primary sodium phosphate, sodium pyrophosphate, sodium sulfate, sodium sulfite, sodium thiosulfate, silver nitrate, zinc sulfate;
lower water-soluble polyethylene glycols such as polyethylene glycols having a molecular weight up to about 600.
Examples for water-insoluble carriers are: vegetable and animal oils such as olive oil, palm oil, fish oil, train oil; animal and vegetable fats such as coconut oil, lard, tallow, spermaceti;
mineral oils and mineral oil products such as paraffine oil, petroleum, Vaseline (Registered Trade Mark), stearin;
inorganic carriers such a diatomaceous earth, Aerosil (Registered Trade Mark), talcum, asbestos, rock wool, silk;
organic insoluble carriers such as wood flour, cellulose, wood pulp, textile fibers.
Water-swellable carriers are plant rubbers such as gum arabic, tragant, alginates, karaya;
natural or synthetic resins such as shellac, ethyl cellulose, methyl cellulose, carboxymethyl cellulose, dextrines.
When mixing polyvinyl pyrrolidone with carriers, the weight ratio lies between about 1:999 and 999:1; preferred is a weight ratio of polyvinyl pyrrolidone to carrier in the range of about 10/90 to 90/10 and especially of about 25/75 to 75/25.
In spray compositions, the smellremoving polyvinyl pyrrolidone is preferably used in amounts of 0.3 to 5% by weight, more preferably 0.5 to 3% by weight and especially 1 to 2% by weight of the total spray composition without propellant.
In lotions, the polyvinyl pyrrolidone is preferably employed in amounts of 0.1 to 5% by weight, more preferably 0.5 to 3% by weight and especially 1 to 2% by weight of the total lotion.
In tablets, the polyvinyl pyrrolidone may normally be employed in amounts of 0.1 to 99.9% by weight, preferably 10 to 99.0% by weight and especially 40 to 98% by weight of the tablet.
The smell-removing agent may be used in combination with typical smell-improving additives for technical, cosmetic, medical and hygienic fields. Examples for these known additives are taste-improving agents, flavours. perfumes, fixatives, anti-oxidants, preservatives, dyes, solvents and/or dispersion bases such as creams or lotions. The mentioned materials are employed in usual concentrations.
When using the smell-removing agent in deodorizing compositions, the concentration of the aqueous and/or alcoholic solution of polyvinyl pyrrolidone or of the mixture of polyvinyl pyrrolidone with carriers normally amounts to about 5 to 100% by weight, preferably 10 to 100% by weight and especially 20 to 100% by weight of the total composition.
The use of polyvinyl pyrrolidone in the above mentioned concentrations results in smell-removing compositions which completely remove bad odours for long periods, i.e. for 24 hours or longer. Polyvinyl pyrrolidone is especially suited for removing odours considered unpleasant, repulsive, nauseous or otherwise offensive by humans and animals.
Polyvinyl pyrrolidone used as sole active substance in alcoholic or aqueous solutions (as deodorant spray for arm-pits, feet etc.) can give complete freedom of body odours for an entire day. Should a smell of sweat have developed already, it can be spontaneously removed when sprayed once with the present solution. If an aqueous solution of polyvinyl pyrrolidone in any concentration is then used for washing. followed by rinsing with clear water, the typical smell may disappear completely and not return.
The same spraying solution also removes the smell of onions or pickled herrings from hands.
Even the smell of rotting flowers or
decaying meat, of feces, or offensive odours from garbage cans as well as undesirable
kitchen odours may be removed.
The same applies to tobacco smoke,
cadaverous smells, bad breath especially
that caused by suppurating wounds in the
mouth, and strong-smelling cheese.
When using polyvinyl pyrrolidone as
smell-removing agent, the final composition may also contain perfume oils which will fully release their individual scent without being impeded by the active compound; the addition of cosmetic oils for skin-care is also possible and will not interfere with the smell-removing effect of the composition.
The following examples are illustrative of the present invention. Unless otherwise stated, all parts are parts by weight. In each
Example, the polyvinyl pyrolidone sample was one producing a k-value of 60.
Example I
A deodorant spray is prepared by dissolving 1.0 parts of polyvinyl pyrrolidone and 0.5 parts of perfume oil in 28.5 parts of alcohol. The solution containing the active substance is then filled into containers in a conventional way while adding 35.0 parts of
Frigen 11 and 35.0 parts of Frigen 12 as propellant (Frigen is a Registered Trade Mark).
Example 2
A deodorant spray is prepared by dissolving 0.5 parts of polyvinyl pyrrolidone, 1.5 parts of isopropyl myristate and 0.5 parts of perfume oil in 28.5 parts of ethanol. The solution containing the active substance is then filled into containers by conventional means, adding 70.0 parts of Frigen 12/114 40/60 as propellant.
Example 3
An aqueous lotion (room spray) for mechanical spraying devices is prepared from 10.0 parts of polyvinyl pyrrolidone, 89.8 parts of water and 0.2 parts of potassium sorbate.
Example 4
A deodorizing mouth-rinse is prepared from 1.0 parts of polyvinyl pyrrolidone, 98.7 parts of distilled water, 0.2 parts of potassium sorbate as preservative and 0.1 parts of saccharine.
Example 5
The hands of several test-persons were contacted with freshly cut onion pieces.
After rinsing with water, the hands still had a specific and rather penetrating smell.
Even repeated washing with water and soap could not remove this smell; it seemed to be fixed in a chemosorptive way to the keratin of the skin.
When the hands were washed once with an aqueous 1% solution of polyvinyl pyrrolidone and rinsed with clear water, the typical smell disappeared completely and did not return.
Example 6
A solution of polyvinylpyrrolidone in water (3% by weight) was applied to the arm pits of several test persons; already existing body odour was removed completely and did not return for 24 hours. The protection against body odour given by the present agent lasts about 14 hours longer than with commercial compositions on the basis of antiseptic substances.
Example 7
Polyvinyl pyrrolidone powder as delivered by the manufacturer was diluted to the use-concentration by stirring 2 grams of the compound into 98 grams of water.
Example 8
The solution of Example 7 was employed in the following tests: (a) Filleted fish was placed into the solution for a short time, i.e. less than 1 minute.
After removal of the fillets from the solution, the typical fish odour had disappeared completely.
(b) An offensively smelling dish rag was immersed into the solution and squeezed several times to ensure thorough wetting.
This took no more than 1 minute. After removal, the dish rag was completely odourless.
(c) Rotting stems of, for instance, orchids and poppies which develop an especially repulsive and penetrating smell, were dipped into the solution for a short time, and the vases were also cleaned with the solution. After this treatment, the offensive smell had disappeared.
(d) Meat, the surface of which showed some decay was placed into the solution for about 2 minutes and then rinsed with clear water.
The mould which had already appeared as well as the black discoloration of the surface and the nauseous odour were completely gone. The meat was again edible.
(e) A sausage which had been stored for 14 days showed mould at the cut surface and its skin was smeary. After having been placed into the solution for 2 minutes, the mentioned superficial traces of decay had disappeared and the sausage could be eaten.
(f) Natural skin for sausages had a bad odour and was smeary. It was placed into the solution where the mentioned defects disappeared completely. The hands of the person conducting this test did also become odourless.
(g) Hands which had been in contact with pickled herrings were in vain washed several times with water and soap. After immersing the hands into the solution and drying them, no smell could be detected, and the smell did not return.
(h) Within a period of 6 months, fifty persons of both sexes and of different ages were cured of an especially repulsive type of bad breath. This odour known as "foetor ex ore" is caused by gingivitis, stomatitis ulcerosa, dentitio difficile, infected tooth extraction wounds and the like. The test-persons rinsed their mouths vigorously with the above solution. The odour was removed spontaneously and completely. No undesirable side-effects were observed.
Example 9
A room spray was prepared by dissolving 2 grams of polyvinyl pyrrolidone in 90 grams of isopropyl alcohol, 5 grams of triethylene glycol and 3 grams of perfume oil. The solution containing the active substance was then filled into containers while 15 grams of
Frigen 11/12 and 7.5 grams of carbonic acid were added as propellant.
Example 10
For the following tests, the person conducting the test held the spray container of
Example 9 over the head and walked around the room to be treated.
(a) The smell of human feces in an especially serious case of pathological diarrhoea was removed rapidly and completely from a toilet, as well as the smell of a cat's feces from a room.
(b) The effectiveness of the spraying composition against kitchen odours was tested with
(1) garlic,
(2) onions,
(3) sauerkraut,
(4) radish salad,
(5) strong-smelling cheese, and
(6) stewed fish.
All odours disappeared completely.
(c) Tobacco smoke of any kind (cigarettes, cigars, pipe) was removed immediately and completely.
(d) The smell of garbage was removed spontaneously and lastingly from a wastedisposer shaft as well as from garbage cans and other containers.
(e) Rotting potatoes were sprayed and were then odourless.
(f) Liver was left to decay in a closed glass container. When the liver was completely liquefied, the container was opened in the open air. Only persons having a rather insensitive stomach could approach the container. After spraying with the above composition, the container could be brought close to the nose, and no repulsive odour could be detected.
(g) After a room had been carpeted, an offensive odour remained which could be removed by spraying with the above composition.
(h) A laboratory was sprayed with ammonia and formaldehyde, respectively, until the test persons showed serious irritations of eyes and respiratory tracts. The above spraying composition was then used and the persons left the room for 3 minutes. When entering again, they could only detect a slight perfumation of the air.
Example 11
A spraying composition for rooms and textiles was prepared by dissolving 5 parts of glycerol, 2. parts of polyvinyl pyrrolidone and 3 parts of perfume oil in 90 parts of isopropyl alcohol. The solution was then filled into containers, adding 5 parts of carbon dioxide as propellant.
Example 12
The composition according to Example 11 was tested as follows: (a) Heavy fuel oil, freshly cut onion rings and camphor, respectively, were placed upon the bottom of glass containers provided with a lid.
(b) Patches of coarse wool cloth having a size of about 1,5 sq. in. each, were suspended close above the surface of the test substance.
(c) After remaining in the containers for 2 hours, the cloth patches were removed and sprayed with the above composition.
(d) After 5 minutes in the open air, the patches were examined and proved completely odourless.
Example 13
Only one side of a wool sweater showing strong signs of perspiration was sprayed with the composition of Example 11; the sweater was left in the open air over night.
The treated side was then odourless while the other side still smelled "sweaty".
Example 14
A tablet against mouth and stomach odours was prepared by compressing 0.5 grams of polyvinyl pyrrolidone and 0.5 grams of sorbite.
After drinking beer and eating fish, test persons took one tablet each and let it dissolve in the mouth. Bad breath was removed immediately. In a second test, the dissolved tablet was swallowed with some mineral water. In this way, even offensive odours arising from the stomach could be removed.
Example 15
The deodorizing spraying compositions of
Examples 1 and 2 were used on about 100 test persons and resulted in spontaneous removal of perspiration odours from arm pits and feet. When treating one side of the test person with commercial products and the other side with a composition in accordance with the present invention, the present compositions proved superior with regard to compatibility and duration of the effect.
Commercial products often caused allergic reactions and resulted in a reddening of the arm pit; this was never the case with the present compositions. They could even be applied to already irritated parts of the body without interfering with the healing process.
The effectiveness of the present compositions normally lasts two- to four-times longer with commercial products.
Example 16
A deodorizing body spray was prepared by dissolving 2 parts of polyvinyl pyrrolidone and 1 part of perfume oil in 92 parts of isopropyl alcohol. The solution containing the active substance was then filled into containers under addition of 5 parts of carbon dioxide as propellant.
WHAT I CLAIM IS:
1. A method for deodorizing comprising contacting matter requiring to be deodorised with polyvinylpyrrolidone (PVP) dissolved or dispersed in a suitable carrier.
2. A method according to claim 1 wherein said PVP is dissolved in a solvent comprising water and/or an alcohol.
3. A method according to claim 1 wherein 0.1 - 75 parts by weight of PVP are dissolved in 99.9 - 25 parts by weight of solvent.
4. A method according to claim 2 or claim 3 wherein a solution of PVP is sprayed into or over matter to be deodorised.
5. A method according to claim 4 wherein the PVP is sprayed from an "aerosol" container by means of a propellant.
6. A method according to claim 1 wherein said PVP is dispersed in a carrier, the weight ratio of PVP: carrier being within the range 1:999 to 999:1.
7. A method according to any one of the preceding claims wherein said carrier has a perfume dissolved or dispersed therein.
8. A method according to any one of the preceding claims wherein the PVP has a k-value in the range 5-150.
9. A method according to any one of the peceing claims wherein the PVP is administered orally.
10. A method of deodorising substantially as any exemplified in the Examples.
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (10)
1. A method for deodorizing comprising contacting matter requiring to be deodorised with polyvinylpyrrolidone (PVP) dissolved or dispersed in a suitable carrier.
2. A method according to claim 1 wherein said PVP is dissolved in a solvent comprising water and/or an alcohol.
3. A method according to claim 1 wherein 0.1 - 75 parts by weight of PVP are dissolved in 99.9 - 25 parts by weight of solvent.
4. A method according to claim 2 or claim 3 wherein a solution of PVP is sprayed into or over matter to be deodorised.
5. A method according to claim 4 wherein the PVP is sprayed from an "aerosol" container by means of a propellant.
6. A method according to claim 1 wherein said PVP is dispersed in a carrier, the weight ratio of PVP: carrier being within the range 1:999 to 999:1.
7. A method according to any one of the preceding claims wherein said carrier has a perfume dissolved or dispersed therein.
8. A method according to any one of the preceding claims wherein the PVP has a k-value in the range 5-150.
9. A method according to any one of the peceing claims wherein the PVP is administered orally.
10. A method of deodorising substantially as any exemplified in the Examples.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2557365A DE2557365C2 (en) | 1975-12-19 | 1975-12-19 | Use of polyvinylpyrrolidone to quench unwanted odors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1571517A true GB1571517A (en) | 1980-07-16 |
Family
ID=5964921
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB48187/76A Expired GB1571517A (en) | 1975-12-19 | 1976-12-16 | Deodorizing composition and method |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JPS5279029A (en) |
| AT (1) | ATA868176A (en) |
| BE (1) | BE849182A (en) |
| CA (1) | CA1076475A (en) |
| CH (1) | CH622700A5 (en) |
| DE (1) | DE2557365C2 (en) |
| FR (1) | FR2335260B1 (en) |
| GB (1) | GB1571517A (en) |
| IT (1) | IT1064474B (en) |
| NL (1) | NL7613664A (en) |
| SE (1) | SE436968B (en) |
| ZA (1) | ZA766967B (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002055114A1 (en) * | 2001-01-09 | 2002-07-18 | Schuer Joerg P | Method for neutralising odours in the air in a non-toxic manner |
| US7108879B2 (en) | 1995-03-31 | 2006-09-19 | Jorg Peter Schur | Process for improving the durability of, and/or stabilizing, microbially perishable products |
| US7323187B1 (en) | 1999-08-27 | 2008-01-29 | Schuer Joerg Peter | Impregnation method |
| US7638114B1 (en) | 1999-07-07 | 2009-12-29 | Schuer Joerg Peter | Method for disinfecting the air |
| CN113264633A (en) * | 2021-04-20 | 2021-08-17 | 广西壮族自治区环境保护科学研究院 | Ecological restoration method for black and odorous river channel |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57166167A (en) * | 1981-04-07 | 1982-10-13 | Hitachi Ltd | Deodorant |
| EP0101083A1 (en) * | 1981-09-22 | 1984-02-22 | Wilhelm O. H. Grunert | Process for neutralising irritants and toxic gases and for preparations suitable for carrying out the process |
| DE3347742A1 (en) * | 1983-12-30 | 1985-07-11 | IG Sprühtechnik GmbH, 7867 Wehr | Deodorising spray |
| JP2006149892A (en) * | 2004-11-30 | 2006-06-15 | Lion Corp | Composition for suppressing urine odor |
| JP5825053B2 (en) * | 2010-11-17 | 2015-12-02 | ライオン株式会社 | Liquid-based sweat deodorant composition |
| DE102016225736A1 (en) | 2016-12-21 | 2018-06-21 | Henkel Ag & Co. Kgaa | Anhydrous deodorant compositions with absorber combination I |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH56377A (en) * | 1911-06-26 | 1912-11-01 | Masch Vertriebs Ges Mit Besch | Paper roll carriers for copier machines |
| DE899248C (en) * | 1944-07-27 | 1953-12-10 | Basf Ag | Cosmetic preparations and processes for their manufacture |
| DE873891C (en) * | 1944-07-27 | 1953-04-20 | Basf Ag | Cosmetic preparations |
| AT196853B (en) * | 1956-04-30 | 1958-03-25 | Fritz Dr Hettinger | Process for the formation of aerosols |
| US3431208A (en) * | 1965-11-17 | 1969-03-04 | Schering Corp | Denture spray |
| DE1767875A1 (en) * | 1968-06-26 | 1971-09-30 | Kuerner Rudolf Dr Dipl Chem | Body care product with a deodorizing effect |
| DE2158463A1 (en) * | 1971-11-25 | 1973-05-30 | Schwarzkopf Gmbh Hans | Aerosol compsn - contg film-former and phasing out agent to delay release of active ingredient |
| DE2263509C2 (en) * | 1972-12-27 | 1981-12-24 | Rudolf Dr. 6380 Bad Homburg Kürner | deodorant |
| US3923974A (en) * | 1973-04-23 | 1975-12-02 | Sterling Drug Inc | Solid fine crystalline paracetamol polymer complex composition |
| US3851032A (en) * | 1973-04-23 | 1974-11-26 | Sterling Drug Inc | Process of preparing a solid fine crystalline paracetamol polymer complex composition |
| GB1485373A (en) * | 1973-11-08 | 1977-09-08 | Unilever Nv | Antiperspirant composition |
| GB1501862A (en) * | 1974-03-13 | 1978-02-22 | Unilever Ltd | Applicator for a skin treatment composition |
| US3939099A (en) * | 1974-12-26 | 1976-02-17 | Chesebrough-Pond's, Inc. | Fragrance composition |
-
1975
- 1975-12-19 DE DE2557365A patent/DE2557365C2/en not_active Expired
-
1976
- 1976-11-17 SE SE7612860A patent/SE436968B/en not_active IP Right Cessation
- 1976-11-22 ZA ZA766967A patent/ZA766967B/en unknown
- 1976-11-23 AT AT868176A patent/ATA868176A/en not_active Application Discontinuation
- 1976-11-24 IT IT29707/76A patent/IT1064474B/en active
- 1976-11-29 CA CA266,737A patent/CA1076475A/en not_active Expired
- 1976-12-02 FR FR7636366A patent/FR2335260B1/en not_active Expired
- 1976-12-08 NL NL7613664A patent/NL7613664A/en unknown
- 1976-12-08 JP JP51146664A patent/JPS5279029A/en active Granted
- 1976-12-08 BE BE173063A patent/BE849182A/en not_active IP Right Cessation
- 1976-12-15 CH CH1577476A patent/CH622700A5/en not_active IP Right Cessation
- 1976-12-16 GB GB48187/76A patent/GB1571517A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7108879B2 (en) | 1995-03-31 | 2006-09-19 | Jorg Peter Schur | Process for improving the durability of, and/or stabilizing, microbially perishable products |
| US7638114B1 (en) | 1999-07-07 | 2009-12-29 | Schuer Joerg Peter | Method for disinfecting the air |
| US7323187B1 (en) | 1999-08-27 | 2008-01-29 | Schuer Joerg Peter | Impregnation method |
| WO2002055114A1 (en) * | 2001-01-09 | 2002-07-18 | Schuer Joerg P | Method for neutralising odours in the air in a non-toxic manner |
| CN113264633A (en) * | 2021-04-20 | 2021-08-17 | 广西壮族自治区环境保护科学研究院 | Ecological restoration method for black and odorous river channel |
Also Published As
| Publication number | Publication date |
|---|---|
| SE7612860L (en) | 1977-06-20 |
| NL7613664A (en) | 1977-06-21 |
| FR2335260A1 (en) | 1977-07-15 |
| JPS5279029A (en) | 1977-07-02 |
| CA1076475A (en) | 1980-04-29 |
| ATA868176A (en) | 1980-05-15 |
| ZA766967B (en) | 1977-10-26 |
| BE849182A (en) | 1977-04-01 |
| IT1064474B (en) | 1985-02-18 |
| JPS5722589B2 (en) | 1982-05-13 |
| SE436968B (en) | 1985-02-04 |
| CH622700A5 (en) | 1981-04-30 |
| FR2335260B1 (en) | 1981-06-12 |
| DE2557365A1 (en) | 1977-07-28 |
| DE2557365C2 (en) | 1982-05-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |