SE446595B - SELF-INFECTIVE CARPET WITH AN ALKYL PHOSPHATE INFORLIVATE IN THE BACKPROOF - Google Patents
SELF-INFECTIVE CARPET WITH AN ALKYL PHOSPHATE INFORLIVATE IN THE BACKPROOFInfo
- Publication number
- SE446595B SE446595B SE8206616A SE8206616A SE446595B SE 446595 B SE446595 B SE 446595B SE 8206616 A SE8206616 A SE 8206616A SE 8206616 A SE8206616 A SE 8206616A SE 446595 B SE446595 B SE 446595B
- Authority
- SE
- Sweden
- Prior art keywords
- backing
- alkyl
- alkyl phosphate
- carbon atoms
- self
- Prior art date
Links
- 229910019142 PO4 Inorganic materials 0.000 title claims description 10
- 239000010452 phosphate Substances 0.000 title claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title 1
- -1 alkyl phosphate Chemical compound 0.000 claims description 21
- 229920003023 plastic Polymers 0.000 claims description 19
- 239000004033 plastic Substances 0.000 claims description 19
- 239000000463 material Substances 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 230000012010 growth Effects 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 239000004800 polyvinyl chloride Substances 0.000 claims description 5
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 4
- 239000002174 Styrene-butadiene Substances 0.000 claims description 3
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- 244000005700 microbiome Species 0.000 claims description 3
- 239000011115 styrene butadiene Substances 0.000 claims description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 230000000717 retained effect Effects 0.000 claims 1
- 239000000654 additive Substances 0.000 description 14
- 230000000996 additive effect Effects 0.000 description 11
- 239000000645 desinfectant Substances 0.000 description 11
- 239000004698 Polyethylene Substances 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 5
- 241000894006 Bacteria Species 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920001817 Agar Polymers 0.000 description 3
- 241000228245 Aspergillus niger Species 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 241000222122 Candida albicans Species 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 241000191940 Staphylococcus Species 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 229940095731 candida albicans Drugs 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 241000194107 Bacillus megaterium Species 0.000 description 1
- 241001478240 Coccus Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 241000588722 Escherichia Species 0.000 description 1
- 241000588748 Klebsiella Species 0.000 description 1
- 241000588915 Klebsiella aerogenes Species 0.000 description 1
- 241000191938 Micrococcus luteus Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000607142 Salmonella Species 0.000 description 1
- 241001138501 Salmonella enterica Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 241000193996 Streptococcus pyogenes Species 0.000 description 1
- 241001045770 Trichophyton mentagrophytes Species 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940092559 enterobacter aerogenes Drugs 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000010137 moulding (plastic) Methods 0.000 description 1
- 239000006916 nutrient agar Substances 0.000 description 1
- 230000005789 organism growth Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/34—Shaped forms, e.g. sheets, not provided for in any other sub-group of this main group
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/5205—Salts of P-acids with N-bases
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Polymers & Plastics (AREA)
- Toxicology (AREA)
- Textile Engineering (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Saccharide Compounds (AREA)
Description
10 15 20 25 30 35 40 446 595 pe de höga temperaturernainom formningen av plastmaterial utan att förlora sin verkan, och som förblir verksamt under en lång tids- rymd. 10 15 20 25 30 35 40 446 595 pe the high temperatures in the molding of plastic materials without lose their effectiveness, and which remain active for a long period of time space.
Ytterligare ett syftemål hos uppfinningen är att tillhanda- hålla ett desinfektionsmedel som är relativt billigt och som icke erfordrar några speciella processer eller förfaranden vid hanteringen.A further object of the invention is to provide keep a disinfectant that is relatively inexpensive and that does not require any special processes or procedures at the handling.
Ett vidare syftemål hos uppfinningen är att tillhandahålla ett desinfektionsmedel som i en låg procenthalt kan införlivas i synnerligen varierande plastmaterial utan att ogynnsamt på- verka plastmateríaletslinneboende egenskaper. Ännu ett syftemål hos uppfinningen är att tillhandahålla ett desinfektionsmedel som är verksamt mot såväl grampositiva som gramnegativa bakterier över ett utbrett haltområde.A further object of the invention is to provide a disinfectant that can be incorporated in a low percentage in highly variable plastic materials without adversely affecting work plastic material linen-dwelling properties. Yet another object of the invention is to provide a disinfectant that is effective against both gram-positive as gram-negative bacteria over a wide range of concentrations.
'Det utgör även ett syftemål hos uppfinningen att tillhanda- hålla ett självdesinfekterande plastmaterial som kan formas, gju- tas, blåsas, strängsprutas eller kalandreras. Ett syftemål enligt uppfinningen utgör även att tillhandahålla ett plastunderlag för mattor som gör den övre ytan av mattan självdesinfekterande.It is also an object of the invention to provide keep a self-disinfecting plastic material that can be molded, taken, blown, extruded or calendered. A purpose according to the invention also constitutes to provide a plastic base for carpets that make the upper surface of the carpet self-disinfecting.
Det har visat sig att vissa alkylfosfatderivat kan disper- geras i ett vätskeformigt eller smält plastmaterial och ge spe- ciella fungicida och baktericida egenskaper åt plastmateríalet, och att desinfekterande egenskaper förblir varaktiga efter det att plastmaterialet gjutits, kalandrerats, formats eller på annat sätt-bearbetats medelst metoder inom plastformningen. Alkylfosfat- derivaten kan inblandas i vätskeformiga polymerer, såsom disper- sioner av polyvinylklorid (PVC), därefter genomförd smältning- och kflandrering den framställda polyvínylfilmen eller -belägg- ningen uppvisar de unika baktericida egenskaperna och är verk- sam mot såväl grampositiva som gramnegatíva organismer, inne- fattande då Pseudomonas aeruginosa. Andra exempel på plastmate- rial, i vilka alkylfosfatderivaten enligt uppfinningen kan finna användning utgöres av polyeten, cellulosaacetatbuterat, polyole- finer, polypropener, polystyren, olika fenolhartser och polysty- renbutadien. Användning kan även förekomma i epoximaterial, akrylmaterial, polyvinylacetat och andra hartser och polymeremul- sionerl Den mängd av alkylfosfat som införlivas i plastblandningen kan varieras beroende på den specifika användningen och den spe- cifika organism som avses att inhiberas. Provningsresultat visar dock, att alkylfosfatderivatet vanligen är tillräckligt verk- 15 20 3% 446 595 samt när mindre än en viktprocent av plastmaterialets vikt an- vändes. Ytterligare mängder från en hundradels procent (0,01 %) till 10 procent (10 l) hur prövats och hur gett effektiva resul- tat under speciella förhållanden.It has been found that certain alkyl phosphate derivatives can disperse made into a liquid or molten plastic material and give specific fungicidal and bactericidal properties of the plastic material, and that disinfectant properties remain durable thereafter that the plastic material has been cast, calendered, shaped or otherwise method-processed by methods in plastic molding. Alkyl phosphate the derivatives can be blended into liquid polymers, such as dispersions. polyvinyl chloride (PVC), then carried out and modifying the produced polyvinyl film or coating. exhibits the unique bactericidal properties and is effective against both gram-positive and gram-negative organisms, including grasping then Pseudomonas aeruginosa. Other examples of plastic in which the alkyl phosphate derivatives of the invention can be found use consists of polyethylene, cellulose acetate butyrated, polyol veneers, polypropylenes, polystyrene, various phenolic resins and polystyrene renbutadiene. Use may also occur in epoxy materials, acrylic materials, polyvinyl acetate and other resins and polymer emulsions The amount of alkyl phosphate incorporated into the plastic mixture may vary depending on the specific use and the specific specific organism intended to be inhibited. Test results show however, that the alkyl phosphate derivative is usually sufficiently effective 15 20 3% 446 595 and when less than one% by weight of the weight of the plastic material is used turned. Additional amounts from one hundredth of a percent (0.01%) to 10 percent (10 l) how tried and how yielded effective results under special conditions.
Alkyfiosfatderivaten enligt föreliggande uppfinning kan åskåd- liggöras av den allmänna formeln vari R betecknar alkyl med upp till 18 kolatomer, R1 betecknar alkyl eller hydroxísubstituerad alkyl med upp till 18 kolatomer, R2 har samma betydelse som R1, R3 betecknar alkyl med upp till 18 kolatomer, och R4 har samma betydelse som RS. Exempel på be- tydelser för R-grupperna visas i följande schema: _3- R1 Rz _ Rs R4 -CxHZX+1 -CH3 -CH3 -ø-CXH2x+1 «ø-CXH2X+1 -CXHZX-OH CXHZX-OH vari x=l-18 vari x=1-18 vari x=1-18 vari x=1-18 vari x=1-18 De mest föredragna alkylfosfatderivaten har visat sig vara de följande: varvid den föredragna mängden utgör 0,10-1 viktprocent, räknat på vikten av det plastmaterial, till vilken det sättes.The alkyphosphate derivatives of the present invention can be is made by the general formula wherein R represents alkyl having up to 18 carbon atoms, R1 represents alkyl or hydroxy-substituted alkyl having up to 18 carbon atoms, R 2 has the same meaning as R 1, R 3 represents alkyl of up to 18 carbon atoms, and R 4 has the same meaning as R 5. Examples of meanings for the R groups are shown in the following scheme: _3- R1 Rz _ Rs R4 -CxHZX + 1 -CH3 -CH3 -ø-CXH2x + 1 «ø-CXH2X + 1 -CXHZX-OH CXHZX-OH vari x = l-18 vari x = 1-18 vari x = 1-18 vari x = 1-18 vari x = 1-18 The most preferred alkyl phosphate derivatives have been found to be the following: wherein the preferred amount is 0.10-1% by weight, calculated on the weight of the plastic material to which it is added.
Föreliggande uppfinning har visat sig verksamt inhibera tillväxten av såväl grampositiva som gramnegativa organismer, och har visat sig vara verksam mot Sarcina lutea, Staphylo- coccus aureus, Staphylococcus ulbus, Pseudomonas aeruginosa, Escherichia coli, Klebsíella, Candida albicans, Salmonella choleraesuis,Enterobacter aerogenes, Escherichia communior, 10 15 20 ZS 30 35 40 446 595 4 Streptococcus pyogenes, Bacillus megaterium, Aspergillus niger och andra.The present invention has been found to effectively inhibit the growth of both gram-positive and gram-negative organisms, and has been shown to be effective against Sarcina lutea, Staphylococcus coccus aureus, Staphylococcus ulbus, Pseudomonas aeruginosa, Escherichia coli, Klebsíella, Candida albicans, Salmonella choleraesuis, Enterobacter aerogenes, Escherichia communior, 10 15 20 ZS 30 35 40 446 595 4 Streptococcus pyogenes, Bacillus megaterium, Aspergillus niger and other.
Vid inblandning av det valda tillsatsmedlet i ett plastma- terial väljes en lämplig mängd av det desinfekterande medlet .eller tillsatsen. Om exempelvis 1 000 kg tabletter av polyeten- harts skall inhiberas, kan 1 kg av tillsatsen väljas och sättas till en trumlande blandningsapparat som innehåller -polyetentab1et- terna. Under den trumlande blandningsprocessen bildar den före- dragna utföringsform av tillsatsen som visas ovan en oljig be- läggning på plasttabletterna och fäster som resultat av detta vid tabletterna. Efter blandning under ca 15 minuter är till- satsen homogent kombinerad med plasttabletterna av polyeten, och de belagda tabletterna kan som sådana förvaras eller transporte- ras, och ingen separation uppkommer mellan tillsatsen och tablet- terna; Även detta utgör en bestämd fördel över de tidigare kända systemen, där tvâ eller flera tillsatser användes för att inhi- bera såväl grampositiva som gramnegativa mikroorganismer, efter- som blandningssvårigheter och utskiljning har visat sig utgöra en allvarlig olägenhet hos tidigare kända metoderÄ_Vätskeformiga polymerer eller polymerblandningar kan även användas med före- liggande uppfinning, ehuru plasttahletterna eller -pärlorna utgör den föredragna formen av plastmaterial för användning i uppfin- ningen.When mixing the selected additive in a plastic material, select an appropriate amount of the disinfectant .or the additive. If, for example, 1,000 kg of polyethylene tablets resin is to be inhibited, 1 kg of the additive can be selected and added a tumbling mixer containing -polyethylene tablet- terna. During the tumbling mixing process, it forms drawn embodiment of the additive shown above an oily coating laying on the plastic tablets and adheres as a result at the tablets. After mixing for about 15 minutes, add the batch homogeneously combined with the plastic tablets of polyethylene, and the coated tablets as such can be stored or transported and no separation occurs between the additive and the tablet terna; This also constitutes a definite advantage over the previously known ones systems, where two or more additives are used to inhibit carry both gram-positive and gram-negative microorganisms, which mixing difficulties and precipitation have been shown to pose a serious inconvenience of prior art methodsLiquid polymers or polymer blends can also be used with the present invention, although the plastic tablets or beads constitute the preferred form of plastic material for use in the invention ningen.
Efter det att polyetentabletterna på ovan beskrivet sätt tillräckligt har blandats med det utvalda tillsatsmedlet, kan tabletterna sedan satsas i en matartratt i en konventionell smältsträngpress, där tabletterna sedan smältes och det desin- fekterande tillsatsmedlet homogent fördelas genom den smälta massan genom inverkan av strängpressen. Den erhållna massan av plastmaterial kan formas till olika utformningar, filmer eller föremål pä konventionellt, käñt sätt. På detta sätt framställda folier eller föremål innehåller en jämn dispersion av tillsats- medlet och har en slät och jämn textur.After the polyethylene tablets as described above sufficiently mixed with the selected additive, can the tablets are then loaded into a hopper in a conventional one melt extruder, where the tablets are then melted and the disintegrated the affecting additive is homogeneously distributed throughout the melt mass by the action of the extruder. The mass obtained from plastic materials can be formed into various designs, films or objects in a conventional, käñt way. Produced in this way foils or articles contain an even dispersion of additives the agent and has a smooth and even texture.
Under värmningen i smältsträngpressen såsom beskrivits ovan, kan temperaturerna uppgå till ZSO°C, ehuru det föredragna områ- det är från 150-ZSOOC, men även vid de högre temperaturerna kan ingen förlust i verkan av det desinfekterande medlet påvisas.During the heating in the melt extruder as described above, temperatures can reach ZSO ° C, although the preferred range is it is from 150-ZSOOC, but even at the higher temperatures can no loss in the effect of the disinfectant is detected.
Det är ofta önskvärt att använda konventionella spinnmun- stycken tillsammans med smältsträngpressar för framställning av termoplastiska fibrer. Föreliggande uppfinning är anpassad för 10 15 20 25 5 446 595 användning med sådan fiberframställníng, och de trådar och garn som kan framställas och innehåller den inhiberande tillsatsen för- hindrar tillväxt av såväl grampositiva som gramnegativa organis- mer på de där av framställda garnen, trådarna och tygerna.It is often desirable to use conventional spinning nozzles. pieces together with melt extruders for the manufacture of thermoplastic fibers. The present invention is adapted for 10 15 20 25 5,446,595 use with such fiber making, and the threads and yarns which can be prepared and contains the inhibitory additive prevents the growth of both gram-positive and gram-negative organisms more on those yarns, threads and fabrics made there.
Ett exempel på genomfönndet av föreliggande uppfinning be- skrives i det följande: En tiondel till 1,5 delar av den föredragna utföringsformen (föredraget alkylfosfatderivat) av det i det föregående visade desinfektionsmedlet sättes till 10 delar polyetentabletter. Tab- letterna belägges med det oljiga tíllsatsmedlet genom trumling av blandningen under 20 minuter. De sålunda behandlade tabletter- na smältes sedan i ett provrör genom att röret nedsänkes i ett oljebad vid 200°C under 20 minuter. Provröret upptages sedan från oljebadet och får svalna till rumstemperatur, varvid den smälta massan stelnar. Den kylda massan uttages sedan från provröret och sågas till skivor med en tjocklek av ca 10 mm. Ingen ned- brytning eller annan ovanlig egenskap hos polyetenskivorna kan påvisas. Skivorna anbringas i lämpligt inympade petriskàlar, innehållande näringsagar. Den agar som på detta sätt inympats med olika organismer ges en inkubatíonstid av 24 timmar vid 37°C med skivorna närvarande för att inhibera tillväxten av bakterierna och svamparna runt skivorna, varvid en inhiberings- zon bildas. Följande resultat erhålles: Tabell A Organism Inhiberingszon 1 mm Staph-aureus 10 Pseudomonas Aeruginosa 4 E. Coli - 6 Klebsiella 8 Candida albicans 10 Salmonella chloreasius 7 Aspergillus niger 10 Trichophyton mentagrophytes 15 Det har visat sig vara speciellt verksamt att framställa en självdesinfekterande matta genom tillsats av det desinfekterande tillsatsmedel till mattunderlagct vid dess framställning. I vissa 10 15 20 25 30 35 446 595 .mattor användes en polyvinylklorídemulsion i underlaget, medan andra mattframställare önskar belägga den framställda mattan med ett hartsmaterial, såsom Styren-butadien eller någon annan poly- merkomposition. I endera fallet kan det desinfekterande alkyl- fosfatderivatet införlivas i underlaget under dess framställning och som sådant tillhandahålla ett desinfektionsmedel för mattun- derlaget och mattans övre yta på grund av kapillärverkan eller attraktion hos garnet vid mattytan. Denna kapillärverkan eller attraktion minskar väsentligt de grampositiva eller gramnega- tiva bakterier, innefattande då Pseudomonas aeruginosa, som kommer i kontakt med mattans övre eller undre yta. Om följakt- ligen en nylonmatta väves och medelst sprutning eller andra me- toder förses med ett styrenunderlag som innehåller alkylfosfat- tillsatsen, kommer garnen eller trådarna av nylon i mattans övre yta genom kapillärverkan att bringa det tillsatsmedel som in- blandats i styren-butadienen att migrera mot de övre delarna av mattans yta och därigenom bilda en matta med desinfekterande ver- kan mot en stor variation av vanliga bakterier och svampar. Som angivits i det föregående, användes olika hartser för att fram- ställa mattunderlag och innefattar polyvinylkloridhartser, sty- ren-butadien, polyolefiner och andra. _ För bestämning av den inhiberande verkan hos det föredragna alkylfosfatderivatet enligt föreliggande uppfinning: c H on c H 'Z 4 e R 12 zs--N--_o--P--oc n I 2 5 c H on OCZHS 2 4 í ett prov av matta på lämpliga provorganismer, användes en lämp- lig ASTM-metod (beteckning: G22-67T), vilken innefattade följande väsentliga steg: 1) Ett provstycke valdes med måtten S x 5 cm, med 100 nylonmatt- garn, smälta till ett polyvínylkloridunderlag.An example of the practice of the present invention is is written in the following: One tenth to 1.5 parts of the preferred embodiment (preferred alkyl phosphate derivative) of the foregoing the disinfectant is added to 10 parts of polyethylene tablets. Tab- the letters are coated with the oily additive by tumbling of the mixture for 20 minutes. The tablets thus treated were then melted in a test tube by immersing the tube in one oil bath at 200 ° C for 20 minutes. The test tube is then picked up from the oil bath and allowed to cool to room temperature, whereby it melts the mass solidifies. The cooled mass is then taken out of the test tube and sawn into slices with a thickness of about 10 mm. No down- refraction or other unusual property of the polyethylene sheets can demonstrated. The slices are placed in suitably grafted petri dishes, containing nutrient agar. The agar inoculated in this way with different organisms, an incubation period of 24 hours is given at 37 ° C with the discs present to inhibit the growth of the bacteria and fungi around the discs, whereby an inhibitory zone is formed. The following results are obtained: Table A Organism Inhibition Zone 1 mm Staph-aureus 10 Pseudomonas Aeruginosa 4 E. Coli - 6 Klebsiella 8 Candida albicans 10 Salmonella chloreasius 7 Aspergillus niger 10 Trichophyton mentagrophytes 15 It has been found to be particularly effective in producing one self-disinfecting carpet by adding the disinfectant additives to carpet substrates in its manufacture. In some 10 15 20 25 30 35 446 595 carpets used a polyvinyl chloride emulsion in the substrate, while other carpet manufacturers wish to coat the manufactured carpet with a resin material, such as styrene-butadiene or another additional composition. In either case, the disinfectant alkyl the phosphate derivative is incorporated into the substrate during its preparation and as such provide a disinfectant for carpet and the upper surface of the mat due to capillary action or attraction of the yarn at the mat surface. This capillary action or attraction significantly reduces the gram-positive or gram-negative active bacteria, including Pseudomonas aeruginosa, which comes into contact with the upper or lower surface of the carpet. If consequential a nylon mat is woven and by spraying or other means is provided with a styrene support containing alkyl phosphate the additive, the yarns or threads of nylon come in the upper of the carpet surface by capillary action to bring the additive contained in mixed in the styrene-butadiene to migrate towards the upper parts of the surface of the carpet and thereby form a carpet with disinfectant can against a wide variety of common bacteria and fungi. As indicated above, various resins were used to produce carpet mats and includes polyvinyl chloride resins, pure butadiene, polyolefins and others. To determine the inhibitory effect of the preferred the alkyl phosphate derivative of the present invention: c H on c H 'Z 4 e R 12 zs - N --_ o - P - oc n I 2 5 c H on OCZHS 2 4 In a sample of carpet on suitable test organisms, a suitable ASTM method (designation: G22-67T), which included the following essential steps: 1) A test piece was selected with the dimensions S x 5 cm, with 100 nylon mats. yarn, melt into a polyvinyl chloride backing.
Z) Testorganismer inympades i kända halter (antal celler per ml) i näringssaltagarmedia, lämplig för deras tillväxt. Varje matt- prov anbringades mellan skikt av sådana inympade agarmedia i petriskålar, en för varje organism. Totalt användes SO-55 ml agar per petriskål. 3] Provstyckaw.inkuberades vid 35-37°C under 12 dygn. Inhiberings- 10 7 446 595 graden på organismtillväxten bestämdes'genom frånvaron av bak- terietíllväxt. 4) Observationer av synliga och fysikaliska påverkníngar på prov- stycket gjordes.Z) Test organisms were inoculated at known levels (number of cells per ml) in nutrient media, suitable for their growth. Every mat- samples were applied between layers of such inoculated agar media in petri dishes, one for each organism. A total of SO-55 ml was used agar per petri dish. 3] Samples were incubated at 35-37 ° C for 12 days. Inhibitory 10 7,446,595 the degree of organism growth was determined by the absence of terietal growth. 4) Observations of visible and physical effects on the sample the paragraph was made.
Resultat: a) Mikrobiell inhibering Använd organism Halt i inympad $ dödade av totala näringssaltagar, antalet organismer celler/ml i ympkulturen (medelvärde från ,två prov)' Staphylococcus aureus 18,5 x 103 100 % Escherichía coli 10,2 x 103 99 $ Bacilius megaterium 13,6 X 103 99 s Pseudomonas aeruginosa 16,3 x 103 99 $ A. niger ingen tillväxt gb) Fysikalíska förändringar i mattstyckena Ingen míkrobiell nedbrytning av mattstyckena kunde obser- veras. Ingen missfärgning förelåg vid tvättning och torkning av provstyckena vid slutet av 12 dygns inkuberingsperiod.Results: a) Microbial inhibition Use organism Content in grafted $ killed by total nutrient salts, number of organisms cells / ml in the inoculum culture (mean from , two tests) ' Staphylococcus aureus 18.5 x 103 100% Escherichía coli 10.2 x 103 99 $ Bacilius megaterium 13.6 X 103 99 s Pseudomonas aeruginosa 16.3 x 103 99 $ A. niger no growth gb) Physical changes in the carpet pieces No microbial degradation of the mat pieces could be observed. veras. No discoloration was present during washing and drying the specimens at the end of the 12 day incubation period.
Olika andra användningsområden och midifíkationer framgår för fackmannen, och de här visade exemplen avser icke att be- gränsa föreliggande uppfinning.Various other uses and midifications appear for the person skilled in the art, and the examples shown here are not intended to limit the present invention.
Claims (3)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8206616A SE446595B (en) | 1982-11-19 | 1982-11-19 | SELF-INFECTIVE CARPET WITH AN ALKYL PHOSPHATE INFORLIVATE IN THE BACKPROOF |
| FR828219893A FR2536632B1 (en) | 1982-11-19 | 1982-11-26 | PROCESS FOR FORMING MATERIALS WITH SELF-HYGIENIC PROPERTIES, BASED ON CATIONIC ALKYL PHOSPHATE DERIVATIVES, AND THEIR USE FOR THE INHIBITION OF MICROBES, ESPECIALLY IN PLASTICS |
| BE0/209611A BE895195A (en) | 1982-11-19 | 1982-11-30 | HEALTH COMPOSITIONS BASED ON ALKYL PHOSPHATES, THEIR PREPARATION AND THEIR USE |
| GB08234072A GB2131029B (en) | 1982-11-19 | 1982-11-30 | Sanitizing of organic polymers |
| AU91364/82A AU567484B2 (en) | 1982-11-19 | 1982-12-09 | Quarternary ammonium phosphate salts incorporated into carpets as sanitizing agent. |
| JP57216252A JPS59106420A (en) | 1982-11-19 | 1982-12-09 | Production of self-disinfectant substance |
| NL8204806A NL8204806A (en) | 1982-11-19 | 1982-12-13 | DISINFECTION AGENTS AND METHODS OF DISINFECTION. |
| AT0468082A AT384630B (en) | 1982-11-19 | 1982-12-23 | ANTIMICROBIALLY EQUIPPED CARPET PRODUCT |
| DE19823248708 DE3248708A1 (en) | 1982-11-19 | 1982-12-31 | PRODUCT WITH ANTI-DISEASE PROPERTIES AND USE OF AN ANTI-GROWTH COMPOUND FOR PRODUCING THE PRODUCT |
| CH28383A CH665521GA3 (en) | 1982-11-19 | 1983-01-19 |
Applications Claiming Priority (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8206616A SE446595B (en) | 1982-11-19 | 1982-11-19 | SELF-INFECTIVE CARPET WITH AN ALKYL PHOSPHATE INFORLIVATE IN THE BACKPROOF |
| FR828219893A FR2536632B1 (en) | 1982-11-19 | 1982-11-26 | PROCESS FOR FORMING MATERIALS WITH SELF-HYGIENIC PROPERTIES, BASED ON CATIONIC ALKYL PHOSPHATE DERIVATIVES, AND THEIR USE FOR THE INHIBITION OF MICROBES, ESPECIALLY IN PLASTICS |
| BE0/209611A BE895195A (en) | 1982-11-19 | 1982-11-30 | HEALTH COMPOSITIONS BASED ON ALKYL PHOSPHATES, THEIR PREPARATION AND THEIR USE |
| GB08234072A GB2131029B (en) | 1982-11-19 | 1982-11-30 | Sanitizing of organic polymers |
| AU91364/82A AU567484B2 (en) | 1982-11-19 | 1982-12-09 | Quarternary ammonium phosphate salts incorporated into carpets as sanitizing agent. |
| JP57216252A JPS59106420A (en) | 1982-11-19 | 1982-12-09 | Production of self-disinfectant substance |
| NL8204806A NL8204806A (en) | 1982-11-19 | 1982-12-13 | DISINFECTION AGENTS AND METHODS OF DISINFECTION. |
| AT0468082A AT384630B (en) | 1982-11-19 | 1982-12-23 | ANTIMICROBIALLY EQUIPPED CARPET PRODUCT |
| DE19823248708 DE3248708A1 (en) | 1982-11-19 | 1982-12-31 | PRODUCT WITH ANTI-DISEASE PROPERTIES AND USE OF AN ANTI-GROWTH COMPOUND FOR PRODUCING THE PRODUCT |
| CH28383A CH665521GA3 (en) | 1982-11-19 | 1983-01-19 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE8206616D0 SE8206616D0 (en) | 1982-11-19 |
| SE8206616L SE8206616L (en) | 1984-05-20 |
| SE446595B true SE446595B (en) | 1986-09-29 |
Family
ID=40349443
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8206616A SE446595B (en) | 1982-11-19 | 1982-11-19 | SELF-INFECTIVE CARPET WITH AN ALKYL PHOSPHATE INFORLIVATE IN THE BACKPROOF |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS59106420A (en) |
| AT (1) | AT384630B (en) |
| AU (1) | AU567484B2 (en) |
| BE (1) | BE895195A (en) |
| CH (1) | CH665521GA3 (en) |
| DE (1) | DE3248708A1 (en) |
| FR (1) | FR2536632B1 (en) |
| GB (1) | GB2131029B (en) |
| NL (1) | NL8204806A (en) |
| SE (1) | SE446595B (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5474739A (en) | 1978-02-04 | 1995-12-12 | Interface, Inc. | Microbiocidal composition |
| US5133933A (en) | 1983-08-16 | 1992-07-28 | Interface Research Corporation | Microbiocidal preservative |
| US4935232A (en) | 1983-08-16 | 1990-06-19 | Interface Research Corporation | Microbiocidal composition and method of preparation thereof |
| US4908209A (en) | 1983-08-16 | 1990-03-13 | Interface, Inc. | Biocidal delivery system of phosphate ester and method of preparation thereof |
| US5032310A (en) | 1983-08-16 | 1991-07-16 | Interface, Inc. | Microbiocidal cleansing and disinfecting formulations and preparation thereof |
| US5024840A (en) * | 1984-03-08 | 1991-06-18 | Interface, Inc. | Antimicrobial carpet and carpet tile |
| CA1334273C (en) * | 1984-10-09 | 1995-02-07 | Robert H. Mcintosh | Microbiocidal composition and method of preparation thereof |
| US4957948A (en) | 1988-05-05 | 1990-09-18 | Interface, Inc. | Biocidal protective coating for heat exchanger coils |
| US5453275A (en) | 1988-05-05 | 1995-09-26 | Interface, Inc. | Biocidal polymeric coating for heat exchanger coils |
| JPH0521766U (en) * | 1991-09-05 | 1993-03-23 | 俊雄 今中 | Vase with mirror |
| EP1960057A4 (en) * | 2005-12-16 | 2013-03-27 | David Kannar | Surface active calcium phosphates |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3247134A (en) * | 1962-07-09 | 1966-04-19 | Owens Corning Fiberglass Corp | Fire retardant cellular polyurethane compositions containing an organic phosphate amine salt |
| US3364192A (en) * | 1964-07-27 | 1968-01-16 | Pfizer & Co C | Antistatic polymer compositions containing ammonium phosphates |
| GB1036578A (en) * | 1963-08-27 | 1966-07-20 | Pfizer & Co C | Tertiary amine salts of phosphoric acid esters |
| US3280131A (en) * | 1964-02-10 | 1966-10-18 | Millmaster Onyx Corp | Quaternary ammonium salts of organophosphorus acids |
| US3920836A (en) * | 1972-09-27 | 1975-11-18 | Askew Anthony B | Sanitizing plastic material |
| DE2654794A1 (en) * | 1976-12-03 | 1978-06-08 | Hoechst Ag | THERMOSTABLE QUATERNAERE AMMONIUM COMPOUNDS FOR FIBER PREPARATION |
| DE3014765A1 (en) * | 1980-04-17 | 1981-10-29 | Henkel Kgaa | Amino hydrohalide antimicrobials - for use as surface disinfectants with a long lasting effect |
| HU184319B (en) * | 1980-08-27 | 1984-08-28 | Borsodi Vegyi Komb | Fungicide compositions salts of phosphonoic acid-monoesters and process for producing the active agents |
-
1982
- 1982-11-19 SE SE8206616A patent/SE446595B/en not_active IP Right Cessation
- 1982-11-26 FR FR828219893A patent/FR2536632B1/en not_active Expired
- 1982-11-30 GB GB08234072A patent/GB2131029B/en not_active Expired
- 1982-11-30 BE BE0/209611A patent/BE895195A/en unknown
- 1982-12-09 AU AU91364/82A patent/AU567484B2/en not_active Expired
- 1982-12-09 JP JP57216252A patent/JPS59106420A/en active Granted
- 1982-12-13 NL NL8204806A patent/NL8204806A/en active Search and Examination
- 1982-12-23 AT AT0468082A patent/AT384630B/en not_active IP Right Cessation
- 1982-12-31 DE DE19823248708 patent/DE3248708A1/en active Granted
-
1983
- 1983-01-19 CH CH28383A patent/CH665521GA3/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6143470B2 (en) | 1986-09-27 |
| NL8204806A (en) | 1984-07-02 |
| CH665521GA3 (en) | 1988-05-31 |
| AU567484B2 (en) | 1987-11-26 |
| SE8206616D0 (en) | 1982-11-19 |
| FR2536632A1 (en) | 1984-06-01 |
| DE3248708A1 (en) | 1984-07-05 |
| SE8206616L (en) | 1984-05-20 |
| JPS59106420A (en) | 1984-06-20 |
| AU9136482A (en) | 1984-06-14 |
| DE3248708C2 (en) | 1988-05-26 |
| BE895195A (en) | 1983-03-16 |
| AT384630B (en) | 1987-12-10 |
| ATA468082A (en) | 1987-05-15 |
| GB2131029A (en) | 1984-06-13 |
| FR2536632B1 (en) | 1989-06-16 |
| GB2131029B (en) | 1986-01-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4683080A (en) | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein | |
| NO174951B (en) | Microbiocide concentrate solution and microbiocide preparation | |
| SE446595B (en) | SELF-INFECTIVE CARPET WITH AN ALKYL PHOSPHATE INFORLIVATE IN THE BACKPROOF | |
| CA2090208A1 (en) | Antibacterial and antifungal polyacetal resin composition | |
| EP0218768A2 (en) | Compositions containing antimicrobial agents in combination with stabilizers | |
| US4110504A (en) | Self-sanitizing carpet construction composition | |
| CN102892824A (en) | Antimicrobial plastic composition and preparation method thereof | |
| CN114213755B (en) | Hydrophobic durable antibacterial polypropylene composite material and preparation method thereof | |
| US4608289A (en) | Carpet containing sanitizing compounds and methods | |
| EP1110948A2 (en) | Polyhexamethyleneguanidine phosphate powder, method of making the same and antimicrobial resin containing the same | |
| KR100379774B1 (en) | Antimicrobial agents, antimicrobial resin compositions, and articles having antimicrobial activity | |
| US4617328A (en) | Biocidal agents for use in plastics, polymers and cellulosic materials | |
| US3360431A (en) | Compositions and method for incorporating microbiocidal amounts of arsenosobenzene into resins | |
| US3197430A (en) | Bacteriostatic acrylonitrile polymers | |
| US4331480A (en) | Biocides for protection of polymeric materials | |
| AU2018285446B2 (en) | Antimicrobial polymer composition | |
| US4711914A (en) | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein | |
| US3198765A (en) | Bacteriostatic acrylonitrile polymers | |
| CN108912478B (en) | Accessory for gondola water faucet | |
| US4758609A (en) | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein | |
| US4721736A (en) | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein | |
| CA1213507A (en) | Use of cationic amino alkyl phosphates as a sanitizer in plastics | |
| US5028619A (en) | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein | |
| US4895877A (en) | Microbiocidal compositions comprising an aryl alkanol and a microbiocidal compound dissolved therein | |
| AU623440B2 (en) | Microbiocidal compositions |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NAL | Patent in force |
Ref document number: 8206616-8 Format of ref document f/p: F |
|
| NUG | Patent has lapsed |
Ref document number: 8206616-8 Format of ref document f/p: F |