WO2012094457A1 - Polyheterosiloxanes for antimicrobial materials - Google Patents
Polyheterosiloxanes for antimicrobial materials Download PDFInfo
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- WO2012094457A1 WO2012094457A1 PCT/US2012/020276 US2012020276W WO2012094457A1 WO 2012094457 A1 WO2012094457 A1 WO 2012094457A1 US 2012020276 W US2012020276 W US 2012020276W WO 2012094457 A1 WO2012094457 A1 WO 2012094457A1
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- 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
- A01N25/08—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 containing solids as carriers or diluents
- A01N25/10—Macromolecular compounds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- C08G77/58—Metal-containing linkages
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- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/14—Paints containing biocides, e.g. fungicides, insecticides or pesticides
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
Definitions
- Antimicrobial materials are of particular interest for a wide variety of applications. Many metals such as tin, zinc, or silver are known for the antimicrobial properties. There is a continuing need to identify compositions and methods for incorporating such metals into surfaces to render them antimicrobial, yet minimize or eliminate the leaching of the metal from the surface during use.
- the present inventors have discovered certain polyheterosiloxane compositions that are useful to render surfaces antimicrobial.
- the polyheterosiloxane compositions comprise at least 70% by weight of:
- a second metal (M2) selected from Zn, Cu, Bi, or Ag
- R 1 is independently a hydrocarbon group or halogen substituted hydrocarbon group containing 1 to 30 carbon atoms
- a may vary from 0.10 to 0.7
- b may vary from 0.001 to 0.5
- c may vary from zero to 0.9
- d may vary from zero to 0.9
- the polyheterosiloxane composition is soluble in an aromatic hydrocarbon solvent.
- the polyheterosiloxane compositions may be used to prepare durable antimicrobial surfaces. DETAILED DESCRIPTION OF THE INVENTION
- polyheterosiloxane compositions of the present invention contain at least 70% by weight of the following components:
- a second metal (M2) selected from Zn, Cu, Bi, or Ag
- Component (A) of the polyheterosiloxane composition is a first metal described by Ml which may be selected from all non-lanthanide metals in the Periodic Table of Elements, providing the metal selected for Ml is different from the second metal (M2).
- Ml is Ti, Zr, Zn, or any combination thereof.
- Ml is Ti.
- the oxidation state of Ml may independently range from 1 to 7. Alternatively, the oxidation state of Ml independently ranges from 1 to 5. Ml in the polyheterosiloxane compositions may have the same or different oxidation states.
- Ml may be bonded to other Ml
- M1 components M2 components, and/or other various organopolysiloxane segments.
- the metals When bonded to other Ml or M2 components, the metals may be linked via oxygen, such as M1-0-M2.
- Ml may have a variety of substituents bonded to it in the present polyheterosiloxane compositions. These substitutes may be residual or un-reacted substituents present on the metal atom in the starting compound used to prepare the polyheterosiloxane, which is discussed below.
- the amount of Ml present in the polyheterosiloxane compositions may vary, providing the amounts are within the mole fractions as detailed below.
- Component (B) of the polyheterosiloxane composition is a second metal described by M2 which may be selected from Zn, Ag, Bi, Cu, or any combination thereof, providing M2 is not the same as Ml.
- the oxidation state of M2 may independently range from 1 to 7. Alternatively, the oxidation state of M2 independently ranges from 1 to 5. M2 in the polyheterosiloxane compositions may have the same or different oxidation states.
- M2 may be bonded to other Ml
- M2 components M2 components, and/or other various organopolysiloxane segments.
- the metals When bonded to other Ml or M2 components, the metals may be linked via oxygen, such as Ml-O-
- M2 may have a variety of substituents bonded to it in the present polyheterosiloxane compositions. These substitutes may be residual or un-reacted substituents present on the metal atom in the starting compound used to prepare the polyheterosiloxane, which is discussed below.
- the amount of M2 present in the polyheterosiloxane compositions may vary, providing the amounts are within the mole fractions as detailed below.
- the polyheterosiloxane compositions of the present invention contain at least some portion that may be considered as organopolysiloxane segments.
- Organopolysiloxanes are polymers containing siloxy units independently selected from (R ⁇ iO ⁇ ), (R 2 S1O 2/2 ), (RS1O 3/2 ), or (S1O 4/2 ) siloxy units, where R may be any monovalent organic group, alternatively R is a hydrocarbon group containing 1 to 18 carbons, alternatively R is an alkyl group containing 1 to 12 carbon atoms, or alternatively R is methyl or phenyl.
- These siloxy units are commonly referred to as M, D, T, and Q units respectively. Their molecular structures are listed below:
- siloxy units can be combined in various manners to form cyclic, linear, or branched structures.
- the chemical and physical properties of the resulting polymeric structures vary depending on the number and type of siloxy units in the organopolysiloxane.
- organopolysiloxane segments composed of D or T siloxy units, that is siloxy units having the formula R ' 2 Si02/2 or R'Si0 3 /2.
- the organopolysiloxane segments may contain other siloxy units, that is any combination of M, D, T, or Q siloxy units, providing at least one D or T unit is present in the organopolysiloxane having the formula R' 2 Si0 2/2 or R'Si0 3/2 .
- R' is independently a hydrocarbon group or halogen substituted hydrocarbon group containing 1 to 18 carbon atoms.
- hydrocarbon groups may have from 1 to 18 carbon atoms, alternatively from 1 to 12 carbon atoms, and are exemplified by, but not limited to alkyl groups such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, undecyl, and octadecyl; cycloalkyl such as cyclohexyl; aryl such as phenyl, tolyl, xylyl, benzyl, and 2- phenylethyl; and halogenated hydrocarbon groups such as 3,3,3-trifluoropropyl, 3- chloropropyl, and dichlorophenyl.
- alkyl groups such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, undecyl, and octadecyl
- the number of siloxy units present in any given organopolysiloxane segment of the polyheterosiloxane composition may vary, providing the amounts are within the mole fractions as detailed below.
- the number and type of siloxy units present will affect the molecular weight of the organopolysiloxane segment, and hence the molecular weight of the polyheterosiloxanes.
- the organopolysiloxane segments of the polyheterosiloxane composition are composed primarily of R'Si0 3/2 siloxy units where R' is phenyl.
- the organopolysiloxane segments of the polyheterosiloxane composition are composed primarily of R' 2 Si0 2/2 siloxy units where one R' substituent is phenyl, and the other R' substituent is methyl.
- the organopolysiloxane segments of the polyheterosiloxane composition is composed primarily of a combination of R' 2 Si0 2/2 and R'Si0 3/2 siloxy units where one R' substituent in the R' 2 Si0 2/2 siloxy unit is phenyl, and the other R' substituent is methyl, R' is phenyl in the R'Si0 3/2 siloxy unit.
- the polyheterosiloxane compositions of the present invention contain at least 70%, alternatively 80%, alternatively 90%, alternatively 95%, or alternatively 98% by weight of components (A), (B), and (C) as described above.
- the amount of components (A), (B), and (C) in the present polyheterosiloxane compositions may vary.
- the varied amounts of each is described by defining the mole fractions of each component relative to the total number of moles of components (A), (B), and (C) present in the polyheterosiloxane composition.
- the mole fraction of components (A), (B), and (C) in the polyheterosiloxane composition relative to each other is of the formula [Ml] a [M2] b [R' 2 Si0 2/2 ] c [R'Si0 3/2 ] d
- a may vary from 0.010 to 0.7
- b may vary from 0.001 to 0.5
- c may vary from zero to 0.9
- d may vary from zero to 0.9
- the terminology " ⁇ " describes that the sum of a+b+c+d is approximately equal to 1.
- the sum may be 0.99, 0.98, 0.97, 0.96, 0.95, etc. If the sum does not equal 1, then the polyheterosiloxane composition may include residual amounts of groups that are not described by the aforementioned formula.
- the number of moles of each component in the polyheterosiloxane composition may be determined using common analytical techniques.
- the number of moles of both Ml and M2 in the polyheterosiloxane composition may be determined using common elemental analysis techniques.
- the number of moles of the siloxy units may be determined by
- the number of moles of each component may be calculated from the amounts of each used in the process to prepare the polyheterosiloxane, and accounting for any losses (such as removal of volatile species) that may occur during the process to produce the polyheterosiloxane.
- polyheterosiloxane compositions to be composed of a complex mixture of various heterosiloxane structures. It is believed that the polyheterosiloxane compositions contain various polymeric structures with Si-O-Si, Si-O-Ml, Ml-O-Ml, and M1-0-M2 linkages as well as Si-0-M2 and M2-0-M2 linkages. However, the concentration of metal to metal links (Ml-O-Ml, M1-0-M2, M2-0-M2) are controlled so as to prevent the formation of metal aggregates or particles of sufficient size to either render the polyheterosiloxanes insoluble in organic solvents, or are of insufficient size to be detected using TEM techniques. Residual alkoxide (-OR) groups also exist on polyheterosiloxane structures and are mainly bonded to
- polyheterosiloxane compositions in an aromatic solvent may contain from 1% to 20% by weight alkoxy groups, alternatively, from 5% to 15% by weight alkoxy groups.
- Residual counter ions from the metal salts (M2) may also be present and are believed to be bonded or chelated to Ml and M2.
- the present polyheterosiloxane compositions are typically soluble in many organic solvents.
- the present polyheterosiloxane compositions are soluble in an aromatic hydrocarbon solvent.
- "soluble" means the present
- polyheterosiloxane compositions dissolve in toluene to form a homogeneous solution having a concentration of at least 1 weight percent of the polyheterosiloxane at 23°C, alternatively having a concentration of at least 5 weight percent of the polyheterosiloxane in toluene at 23°C, alternatively having a concentration of at least 10 weight percent of the
- polyheterosiloxane in toluene at 23°C alternatively having a concentration of at least 20 weight percent of the polyheterosiloxane in toluene at 23°C.
- the present polyheterosiloxane compositions may also be soluble in other organic solvents, such as chloroform, carbon tetrachloride, THF, and butyl acetate.
- the polyheterosiloxanes have molecular weights (weight average) ranging from 1000 to 1,000,000 g/mole, alternatively from 2,000 to 400,000 g/mole, alternatively from 2,000 to 200,000 g/mole.
- the molecular weights may be determined using modified GPC techniques to eliminate possible interactions between the sample and the column system. For example, the molecular weights may be determined by GPC analysis using triple detectors (light scattering, refractometer, and viscometer) with a column (PL 5u 100a 100 x 7.8mm) designed for rapid analysis or Flow Injection Polymer Analysis (FIPA).
- the present polyheterosiloxane compositions may include "metal-rich” domains and "siloxane-rich” domains.
- metal-rich domains describes the structural segments of the polyheterosiloxane compositions where a plurality of linking bonds contain Ml or M2 (that is Ml-O-Ml, M1-0-M2, M2-0-M2, Ml-O-Si, or M2-0-Si).
- siloxane-rich refers to the structural segments of the polyheterosiloxane compositions where a plurality of linking bonds are siloxane (Si-O-Si) bonds.
- the present inventors believe the "metal-rich" domains are such that the amount of metal to metal links (Ml-O-Ml, M1-0-M2, M2-0-M2) are minimized so as to prevent the formation of metal aggregates or particles of sufficient size to prevent their solubility in aromatic hydrocarbons, as discussed above.
- the metal rich domain may not be of sufficient size to be observed using high resolution transmission electron micrograph (TEM).
- the Ml and M2 metals are sufficiently distributed in the polyheterosiloxane compositions and have a domain size smaller than 10 nanometers, alternatively smaller than 5 nanometers, or alternatively smaller than 2 nanometers (detection limits for the TEM).
- the present polyheterosiloxane compositions may be prepared by the methods as taught in PCT application No. PCT/US 10/40510, which is incorporated by reference.
- the present polyheterosiloxanes may be prepared by reacting (AO at least one metal (Ml) alkoxide containing Ti, Zr, or Zn, ( ⁇ ) at least one hydrolyzable metal (M2) salt selected from a non-lanthanide metal series of the Periodic Table , and (C at least one silicon- containing material, with an amount of water that provides between 50 and 200% necessary to hydrolyze and condense the alkoxy groups and other hydrolyzable groups on Components (AO, (B , and (CO, to form the present polyheterosiloxane compositions.
- Component (AO) comprises at least one metal alkoxide containing Ti, Zr, or Zn.
- the metal alkoxide may be selected from metal alkoxides having a general formula (I)
- PJmMlOn Xp iOR ⁇ v 1 - m .p-2n where Ml is selected from Ti, Zr, and Zn, each X is independently selected from carboxylate ligands, organosulfonate ligands, organophosphate ligands, ⁇ -diketonate ligands, and chloride ligands, subscript vl is the oxidation state of Ml, m is a value from 0 to 3, n is a value from 0 to 2, p is a value from 0 to 3, each is a monovalent alkyl group having from 1 to 18 carbon atoms, each is an independently selected monovalent alkyl group having from 1 to 6 carbon atoms, aryl group having from 6 to 8 carbon atoms, or a polyether group having a general formula (VI) -(R ⁇ C qR ⁇ , where q is a value from 1 to 4, each R3 is an independently selected divalent alkylene group having from 2 to 6 carbon
- Rl is a monovalent alkyl group having from 1 to 18 carbon atoms.
- alkyl group of Rl examples include methyl, ethyl, propyl, isopropyl, butyl, t-butyl, hexyl, octyl, decyl, dodecyl, hexadecyl, and octadecyl.
- the alkyl group comprises 1 to 8 carbon atoms.
- the alkyl group is methyl, ethyl, propyl, butyl, hexyl, and octyl.
- each R 2 is an independently selected monovalent alkyl group having from 1 to 6 carbon atoms, aryl group having from 6 to 8 carbon atoms, or a polyether group having a general formula (VI) -(R ⁇ C qR ⁇ , where q is a value from 1 to 4, each R ⁇ is an independently selected divalent alkylene group having from 2 to 6 carbon atoms, R ⁇ is an independently selected hydrogen atom or monovalent alkyl group having from 1 to 6 carbon atoms.
- Examples of the alkyl groups of R 2 include methyl, ethyl, propyl, isopropyl, butyl, t- butyl, and hexyl.
- Examples of the aryl groups of R 2 include phenyl and benzyl.
- Examples of the divalent alkylene group having from 2 to 6 carbon atoms of R ⁇ include -CH2CH2- and -CH2CH(CH3)- .
- Examples of the alkyl groups having from 1 to 6 carbon atoms of R4 are as described above for R 2 .
- Subscript q in Formula (VI) is a value from 1 to 4, alternatively 1 to 2.
- Examples of the polyether group of Formula (VI) include methoxyethyl, methoxypropyl, methoxybutyl, ethoxyethyl, ethoxypropyl, ethoxybutyl, methoxyethoxyethyl, and ethoxyethoxyethyl.
- R 2 is an alkyl group having from 1 to 6 carbon atoms, alternatively ethyl, propyl, and butyl, alternatively propyl and butyl.
- X is selected from carboxylate ligands, organosulfonate ligands, organophosphate ligands, ⁇ -diketonate ligands, and chloride ligands, alternatively
- the carboxylate ligands useful for X have a formula RI ⁇ COO " where R!5 is selected from hydrogen, alkyl groups, alkenyl groups, and aryl groups.
- R!5 is selected from hydrogen, alkyl groups, alkenyl groups, and aryl groups.
- useful alkyl groups for R!5 include alkyl groups having from 1 to 18 carbon atoms, alternatively 1 to 8 carbon atoms as described above for R1.
- Examples of useful alkenyl groups for Rl5 include alkenyl groups having from 2 to 18 carbon atoms, alternatively 2 to 8 carbon atoms such as vinyl, 2-propenyl, allyl, hexenyl, and octenyl.
- Rl5 examples include aryl groups having from 6 to 18 carbon atoms, alternatively 6 to 8 carbon atoms such as phenyl and benzyl.
- R!5 is methyl, 2-propenyl, allyl, and phenyl.
- the ⁇ -diketonate ligands useful for X can have the following structures:
- R 16 Rl8 , and R 21 are selected from monovalent alkyl and aryl groups.
- Examples of useful alkyl groups for R 16 Rl8 , and R 21 include alkyl groups having from 1 to 12 carbon atoms, alternatively 1 to 4 carbon atoms such as methyl, ethyl, trifluoromethyl, and t-butyl.
- Examples of useful aryl groups for R 16 Rl8 , and R 21 include aryl groups having from 6 to
- R!9 is selected from alkyl groups, alkenyl groups and aryl groups.
- useful alkyl groups for R!9 include CI to C18 alkyl groups, alternatively CI to C8 alkyl groups such as methyl, ethyl, propyl, hexyl and octyl.
- useful alkenyl groups for R!9 include alkenyl groups having from 2 to 18 carbon atoms, alternatively C2 to C8 carbon atoms such as allyl, hexenyl, and octenyl.
- aryl groups for R!9 include aryl groups having from 6 to 18 carbon atoms, alternatively 6 to 8 carbon atoms such as phenyl and tolyl.
- R ⁇ and R 20 are hydrogen or alkyl, alkenyl, and aryl groups. Examples of useful alkyl groups for
- R! and R ⁇ O include alkyl groups having from 1 to 12 carbon atoms, alternatively 1 to 8 carbon atoms such as methyl and ethyl.
- alkenyl groups for R!7 and R ⁇ O include alkenyl groups having from 2 to 18 carbon atoms, alternatively 2 to 8 carbon atoms such as vinyl, allyl, hexenyl, and octenyl.
- useful aryl groups for R!7 and R ⁇ O include aryl groups having from 6 to 18 carbon atoms, alternatively 6 to 8 carbon atoms such as phenyl and tolyl.
- R! , R17 ? 18 ? R19 ? 20 ; an d R 21 are each independently selected and can be the same or different.
- subscript vl is the oxidation state of Ml, ranging from 1 to 7.
- vl ranges from 1 to 5.
- subscript m is a value from 0 to 3, alternatively 0 to 2, alternatively 0.
- n is a value from 0 to 2, alternatively 0 to 1, alternatively 0.
- subscript p is a value from 0 to 3, alternatively 0 to 2, alternatively 0.
- Examples of the metal alkoxides described by Formula (I) useful in the present method include titanium tetrapropoxides, titanium tetrabutoxides, zirconium tetrapropoxides, and zirconium tetrabutoxides from DuPont, aluminum tripropoxides, titanium ethoxide, titanium 2-ethylhexoxide, titanium methoxide, titanium methoxypropoxide, titanium n- nonyloxide, zinc methoxyethoxide, zirconium ethoxide, zirconium 2-ethylhexoxide, zirconium 2-methyl-2-butoxide, and zirconium 2-methoxymethyl-2-propoxide, titanium allylacetoacetate triisopropoxide, titanium bis(triethanolamine) diisopropoxide, titanium chloride triisopropoxide, titanium dichloride diethoxide, titanium diisopropoxy bis(2,4- pentanedionate), titanium diis
- zirconium bis-2,2'-(alloxymethyl)- butoxide)tris(dioctylphosphate), zirconium diisopropoxide bis(2,2,6,6-tetramethyl-3,5- heptanedionate), zirconium dimethacrylate dibutoxide, zirconium
- component (A is selected from titanium tetraisopropoxide, titanium tetrabutoxide, or zirconium tetrabutoxide.
- component ( ⁇ ') may be selected from a polymer resulting from the partial hydrolysis and condensation of the metal alkoxides as described above.
- component ( ⁇ ') may be a butyl titanate polymer (such as DuPont TYZOR® BTP), propyl titanate polymer, iso-propyl titanate polymer, sec-butyl titanate polymer, tert- butyl titanate polymer, or zirconate polymers with similar substituents.
- component ( ⁇ ') may be a butyl titanate polymer (such as DuPont TYZOR® BTP), propyl titanate polymer, iso-propyl titanate polymer, sec-butyl titanate polymer, tert- butyl titanate polymer, or zirconate polymers with similar substituents.
- Component ( ⁇ ') may comprise at least one metal (M2) salt selected from (B'l) a non-hydrated metal salt having a general formula (IV) R ⁇ e M2(Z)( v 2- e )/w or a hydrated metal salt having a general formula (V) M2(Z) v 2/ w -xH20, where M2 is selected from Zn, Cu, Bi, or Ag, v2 is the oxidation state of M2, w is the oxidation state of ligand Z where Z is independently chosen from carboxylates, ⁇ -diketonates, fluoride, chloride, bromide, iodide, organic sulfonate, nitrate, nitrite, sulphate, sulfite, cyanide, phosphites, phosphates, organic phosphites, organic phosphates, and oxalate, each is an independently selected alkyl group having 1 to 18 carbon atoms, alken
- the metal element described by M2 is selected from any of the non-lanthanide metals in the Periodic Table of Elements.
- M2 is Zn, Ag or a combination of both.
- subscript v2 is the oxidation state of M2 and can range from 1 to 7, alternatively 1 to 4.
- subscript w is the oxidation state of ligand Z and can range from 1 to 3, alternatively 1 to 2.
- each Z is independently selected from carboxylate ligands, ⁇ -diketonate ligands, fluoride ligand, chloride ligand, bromide ligand, iodide ligand, organic sulfonate ligands, nitrate ligand, nitrite ligand, sulphate ligand, sulfite ligand, cyanide ligand, phosphate ligand, phosphite ligand, organic phosphite ligands, organic phosphate ligands, and oxalate ligand.
- carboxylate ligands and ⁇ -diketonate ligands useful for Z are as described above for X.
- the organic sulfonate ligands useful for Z have a formula R 22 S03 ⁇ , where R 22 S selected from monovalent alkyl groups, alkenyl groups and aryl groups. Examples of useful alkyl groups, alkenyl groups and aryl groups are as described above for Rl5. Alternatively R 22 is tolyl, phenyl, and methyl.
- organic phosphate ligands useful for Z have a formula (R 2 ⁇ 0)2 ⁇ (3 ⁇ 4 " or R 2 30-
- R 23 is selected from monovalent alkyl groups, alkenyl groups and aryl groups.
- R 2 ⁇ is phenyl, butyl, and octyl.
- the organic phosphite ligands useful for Z have a formula (R ⁇ O)2 PO or R ⁇ O- PC"2 ⁇ " , where R2 is selected from monovalent alkyl groups, alkenyl groups and aryl groups. Examples of useful alkyl groups, alkenyl groups and aryl groups are as described above for R!5. Alternatively R ⁇ 4 S phenyl, butyl, and octyl.
- Z in Formulas (IV) and (V) is independently selected from
- Z includes carboxylate ligands and ⁇ -diketonate ligands.
- subscript e is a value from 0 to 3, alternatively 0 to 2, alternatively 0.
- R 7 is an independently selected alkyl group having 1 to 18 carbon atoms, alkenyl group having from 2 to 8 carbon atoms, or aryl group having from 6 to 8 carbon atoms. Examples of R 7 are as described above for R5.
- x is a value from 0.5 to 12, alternatively 1 to 9.
- Examples of ( ⁇ ) metal salts described by Formula (IV) useful in the present method include but are not limited to zinc acetate, zinc acrylate, zinc benzoate, zinc 2- ethylhexoate, silver nitrate, silver benzoate, silver 2-ethylhexanoate, silver neodecanoate, copper acetate, copper acrylate, copper benzoate, copper 2-ethylhexoate, bismuth 2- ethylhexanoate, bismuth neodecanoate, bismuth acetate, and bismuth salicylate.
- Examples of hydrated metal salts ( ⁇ 2) described by Formula (VI) useful in the present method include the hydrated versions of any of the metal salts as listed above for
- ( ⁇ ') is zinc acetate, silver nitrate, or a combination of both.
- both the non-hydrated metal salts and the hydrated metal salts described above are commercially available through the major chemical vendors, such as Sigma-Aldrich, Fisher Scientific, Alfa-Aesar, Gelest.
- Component (C) is a silicon-containing material having hydrolyzable groups selected from (C'l) an organosiloxane , or (C'2) a silane.
- component (C) is at least one silicon-containing material selected from (C'l) an organosiloxane having an average formula (II) R5 g (R6o) f SiO (4 -(f+g))/2 or (C'2) a silane having a general formula (III) R 5 SiZ'i,where Z' is CI or OR 6 , each R5 is an independently selected hydrogen atom, alkyl group having 1 to 18 carbon atoms, alkenyl group having from 2 to 18 carbon atoms, aryl group having from 6 to 12 carbon atoms, epoxy group, amino group, or carbinol group, providing at least one R5 groups on the (C'l) organosiloxane or (C'2) silane selected to produce the present polyheterosiloxane composition
- R 2 S1O 2/2 or R'SiC"3 /2 siloxy units.
- at least one R ⁇ R' in the (C'l) organosiloxane or (C'2) silane component as described by formula (II) or (III).
- Each R 6 is an independently selected hydrogen atom or alkyl group having from 1 to 6 carbon atoms, aryl group having from 6 to 8 carbon atoms, or a polyether group having a general formula (VI) -(R ⁇ C qR ⁇ , where q is a value from 1 to 4, each R ⁇ is an independently selected divalent alkylene group having from 2 to 6 carbon atoms, R4 is an independently selected hydrogen atom or monovalent alkyl group having from 1 to 6 carbon atoms, the subscript f is a value from 0.1 to 3, g is a value from 0.5 to 3, and (f+g) is a value from 0.6 to 3.9, h is a value from 0 to 3, i is a value from 1 to 4 and (h+i) equals 4.
- alkyl groups having 1 to 18 carbon atoms of R ⁇ in Formulas (II) and (III) are as described above for R1.
- the alkyl group comprises 1 to 6 carbon atoms;
- the alkyl group is methyl, ethyl, propyl, butyl, and hexyl.
- alkenyl groups having from 2 to 18 carbon atoms of R ⁇ in Formulas (II) and (III) are illustrated by vinyl, propenyl, butenyl, pentenyl, hexenyl, or octenyl.
- the alkenyl group comprises 2 to 8 carbon atoms.
- the alkenyl group is vinyl, allyl, and hexenyl.
- aryl groups having 6 to 12 carbon atoms of R ⁇ in Formulas (II) and (III) are illustrated by phenyl, naphthyl, benzyl, tolyl, xylyl, methylphenyl, 2-phenylethyl, 2-phenyl- 2-methylethyl, chlorophenyl, bromophenyl and fluorophenyl.
- the aryl group comprises 6 to 8 carbon atoms.
- the aryl group is phenyl.
- subscript f is a value from 0.1 to 3, alternatively 1 to 3.
- subscript g is a value from 0.5 to 3, alternatively 1.5 to 2.5.
- organosiloxanes (C'l) described by Formula (II) and useful in the present method include oligomeric and polymeric organosiloxanes, such as silanol-terminated polydimethylsiloxane, polymethylmethoxysiloxane, polysilsesquioxane, alkoxy and/or silanol containing MQ resin, and combinations thereof. They are made by hydrolysis of the corresponding organomethoxysilanes, organoethoxysilanes, organoisopropoxysilanes, and organochlorosilanes.
- each Z' is a chloro atom (CI) or 0R6, where R6 is as described above.
- Z' is OR ⁇ .
- subscript h is a value from 0 to 3, alternatively, h is a value from 1 to 3, alternatively, from 2 to 3.
- subscript i is a value from 1 to 4, alternatively i is a value from 1 to
- Examples of the silanes (C'2) described by Formula (III) include
- triphenylsilanol phenyldimethoxysilanol, phenylmethoxysilanediol, methyldimethoxysilanol, methylmethoxysilanediol, phenyldiethoxysilanol, phenylethoxysilanediol,
- polyheterosiloxane compositions Component (A and Component ( ⁇ ) are reacted with water to form a mixed metal oxides solution containing M1-0-M2 oxo-linkages, and (2) then further reacting the mixed metal oxides solution with Component (C'l) or (C'2) to form the polyheterosiloxane composition, wherein the total amount of water added is between 50 and 200% of the amount theoretically necessary for the hydrolysis and condensation of all alkoxy groups and other hydrolyzable groups on Components ( ⁇ '), ( ⁇ ), and (CO- [0076] An amount of water must be added in each embodiment so that polyheterosiloxanes having at least two non-Si metal elements are formed.
- water can also be incorporated via the hydrated metal salts (B'2)
- B'2 hydrated metal salts
- a person skilled in the art would understand that when hydrated metal salts are utilized either smaller amounts or no additional amounts of water may need to be added in order for the needed amount of water to be present.
- the amount of water needed for making the present polyheterosiloxanes ranges from 50% to 200% of the theoretical amount of water necessary for complete hydrolysis and condensation of all the alkoxy and other hydrolyzable groups present on each of the components.
- 0.5 mole of water is necessary for hydrolysis and condensation of 1 mole of alkoxy and other hydrolyzable groups.
- the amount of water needed to make the present polyheterosiloxanes ranges from 70% to 150% of the theoretical amount of 3 ⁇ 40 necessary for complete hydrolysis and condensation of all the alkoxy and other hydrolyzable groups present on each of the components, alternatively, 80% to 120% on the same basis.
- the water is added slowly to ensure the metal alkoxide does not react so quickly with the water as to form a precipitate.
- one method of accomplishing this is to dilute the water with solvents.
- the solvents useful for diluting the water are the same as used for dispersing the components.
- the needed water may also be added at one time or during one or more of the steps.
- Other hydrolyzable groups that may be present and need to be hydrolyzed and condensed are any found on the components used, including, but not limited to, chloro.
- the term "dispersion" in the present methods means that the molecules of the various components are homogenously distributed.
- Each of the components may be liquid or solids and so it is preferred that they are pre-mixed or dispersed. Stirring one or more of the components in a solvent is an excellent way to get a homogenous dispersion; or a solvent may not be needed if one or more components can be dispersed in another component.
- any kind of solvent is useful including polar solvents, non-polar solvent, hydrocarbon solvents including aromatic and saturated hydrocarbons, alcohols.
- solvents useful for dispersing Components ( ⁇ '), ( ⁇ '), and (C includes hydrocarbonethanol, 1-propanol, isopropanol, 1-butanol, 2-butanol, methoxyethanol, methoxyethoxyethanol, butyl acetate, toluene, and xylene, alternatively isopropanol, 1- butanol, 2-butanol, and butyl acetate.
- One type of solvent could be used or a mixture of different solvents would also be useful.
- the dispersing or mixing may be done by any conventional means such as stirring.
- the reaction between Components ( ⁇ '), ( ⁇ ), and (C in each of the methods proceeds at room temperature (20°C) but if desired, elevated temperatures up to about 140°C may be used. Alternatively, the temperature can range from 20°C to 120°C. Generally, the reaction can take 30 minutes to 24 hours, alternatively 10 minutes to 4 hours.
- An optional step in all the methods comprises removing the solvent to produce the polyheterosiloxane. The solvents can be removed by any conventional manner such as heating to elevated temperatures or using reduced pressure.
- the polyheterosiloxane can then be redispersed in a solvent of choice such as toluene, THF, butyl acetate, chloroform, dioxane, 1-butanol, and pyridine. Since the Si-O-M linkages made by the present method can be susceptible to hydrolytic cleavage in the presence of 3 ⁇ 4(), to ensure longer shelf life it is preferred to minimize the polyheterosiloxane' s exposure to moisture.
- a solvent of choice such as toluene, THF, butyl acetate, chloroform, dioxane, 1-butanol, and pyridine.
- the present disclosure further provides a method for forming an antimicrobial coating comprising:
- TnBT tetrabutyl titanate
- 21. Og 1-BuOH 20.2g toluene
- 6.43g AgN0 3 were mixed in a 500ml flask. Stirred at RT for ⁇ 2 hours and then added 43.2g solution containing 10% 0.1N HC1 in 1-BuOH. Continued stirring for 1.5 hours at RT. Added a prehydrolyzed siloxane solution that was prepared by mixing 28.50g
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KR1020137017019A KR20140006820A (en) | 2011-01-05 | 2012-01-05 | Polyheterosiloxanes for antimicrobial materials |
JP2013548527A JP2014504667A (en) | 2011-01-05 | 2012-01-05 | Polyheterosiloxane for antibacterial materials |
EP12700586.6A EP2661647A1 (en) | 2011-01-05 | 2012-01-05 | Polyheterosiloxanes for antimicrobial materials |
CN2012800040436A CN103261922A (en) | 2011-01-05 | 2012-01-05 | Polyheterosiloxanes for antimicrobial materials |
US13/885,702 US20130230603A1 (en) | 2011-01-05 | 2012-01-05 | Polyheterosilxoanes For Antimicrobial Materials |
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US201161429973P | 2011-01-05 | 2011-01-05 | |
US61/429,973 | 2011-01-05 |
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US (1) | US20130230603A1 (en) |
EP (1) | EP2661647A1 (en) |
JP (1) | JP2014504667A (en) |
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US11532806B2 (en) | 2014-04-01 | 2022-12-20 | The Research Foundation For The State University Of New York | Electrode materials that include an active composition of the formula MgzMxOy for group II cation-based batteries |
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US10064273B2 (en) | 2015-10-20 | 2018-08-28 | MR Label Company | Antimicrobial copper sheet overlays and related methods for making and using |
CN109221250A (en) * | 2018-10-19 | 2019-01-18 | 东南大学 | A kind of high activity composite nano anti-biotic material and its methods for making and using same |
CN112832028B (en) * | 2021-02-05 | 2023-06-30 | 浙江红督服饰有限公司 | Preparation method of natural antibacterial silk cloth |
CN112826156B (en) * | 2021-02-05 | 2023-12-15 | 江西梦娜袜业有限公司 | Preparation method of socks with deodorizing and antibacterial functions |
Citations (3)
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US1040510A (en) | 1911-10-07 | 1912-10-08 | Chester W Cliff | Steam-generator. |
US4400326A (en) * | 1979-09-24 | 1983-08-23 | Dow Corning Corporation | Aqueous metal ammine siliconate solutions, and amorphous materials derived therefrom, and methods of their use |
WO2011002826A1 (en) * | 2009-07-02 | 2011-01-06 | Dow Corning Corporation | Methods for preparing polyheterosiloxanes |
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US4347347A (en) * | 1979-06-28 | 1982-08-31 | Ube Industries, Ltd. | Crosslinked organometallic block copolymers and process for production thereof |
JPS56159223A (en) * | 1980-05-13 | 1981-12-08 | Seishi Yajima | Production of heat-resistant compound |
JP3899546B2 (en) * | 1996-03-11 | 2007-03-28 | 株式会社豊田中央研究所 | Layered organic titanosilicate and molded body of layered organic titanosilicate |
US6213722B1 (en) * | 1996-03-29 | 2001-04-10 | Davor Jack Raos | Sucker rod actuating device |
JP3846545B2 (en) * | 2000-06-08 | 2006-11-15 | 信越化学工業株式会社 | Coating agent composition, coating method and coated article |
JP4041966B2 (en) * | 2002-06-18 | 2008-02-06 | 信越化学工業株式会社 | Article with hard coat agent and hard coat film formed |
US8425926B2 (en) * | 2003-07-16 | 2013-04-23 | Yongxing Qiu | Antimicrobial medical devices |
US7652157B2 (en) * | 2007-06-22 | 2010-01-26 | General Electric Company | Metal oxide coatings |
GB2459082B (en) * | 2008-02-19 | 2010-04-21 | Phillip Raymond Michael Denne | Improvements in artificial lift mechanisms |
-
2012
- 2012-01-05 EP EP12700586.6A patent/EP2661647A1/en not_active Withdrawn
- 2012-01-05 JP JP2013548527A patent/JP2014504667A/en active Pending
- 2012-01-05 US US13/885,702 patent/US20130230603A1/en not_active Abandoned
- 2012-01-05 CN CN2012800040436A patent/CN103261922A/en active Pending
- 2012-01-05 WO PCT/US2012/020276 patent/WO2012094457A1/en active Application Filing
- 2012-01-05 KR KR1020137017019A patent/KR20140006820A/en not_active Application Discontinuation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1040510A (en) | 1911-10-07 | 1912-10-08 | Chester W Cliff | Steam-generator. |
US4400326A (en) * | 1979-09-24 | 1983-08-23 | Dow Corning Corporation | Aqueous metal ammine siliconate solutions, and amorphous materials derived therefrom, and methods of their use |
WO2011002826A1 (en) * | 2009-07-02 | 2011-01-06 | Dow Corning Corporation | Methods for preparing polyheterosiloxanes |
Cited By (1)
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US11532806B2 (en) | 2014-04-01 | 2022-12-20 | The Research Foundation For The State University Of New York | Electrode materials that include an active composition of the formula MgzMxOy for group II cation-based batteries |
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EP2661647A1 (en) | 2013-11-13 |
CN103261922A (en) | 2013-08-21 |
KR20140006820A (en) | 2014-01-16 |
JP2014504667A (en) | 2014-02-24 |
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