Patent Application
20210363465
This invention relates to a formuation that is a nanostructured and non-toxic material obtained by the sol-gel chemical synthesis method for use as a surface, material and/or personal cleaner.
A great number of surface, material and personal cleaning formulation exist in the prior art.
The present invention however, refers to a formulation comprising nanostructured, biocompatible and biocatalytic material comprising a solid acid consisting of mixed oxides of silica and titania (TiO2—SiO2); supporting in its dispersed matrix: copper, silver, gold, iron, rutenium, palladium, zinc, manganese, iridium and/or platinum metals at minimal concentrations, for use in surface, material and personal cleaning.
In the past decade, scientists' ability to manipulate materials at the molecular and atomic levels using nanotechnology has moved from science fiction into scientific fact. Now, nanotechnology is being developed to prevent, diagnose, and treat infectious diseases, with some products in or nearing clinical trial stage. Progress in this field is exponential. Cross-disciplinary nanoscience and nanomedicine researches involving chemists, physicists, biologists and engineers is concerned about the need for developing environmentally friendly and sustainable methods for the synthesis of nanomaterials. There is a current drive to integrate all the green chemistry approaches to design environmentally benign materials and processes. Rapid developments are taking place in the synthesis of biocompatible mixed oxides or simple oxides metallic and bimetallic nanomaterials and their surface modification for bioactivity and nanomedical applications. Biosynthesis of nanoparticles as an emerging highlight of the intersection of nanotechnology and biotechnology has received increased attention due to a growing need to develop environmentally benign technologies in material syntheses. Biomolecules as reluctant are found to have a significant advantage over their counterparts as protecting agents.
The properties of the materials can change notably when its particle size is reduced to particles in the scale of nanometers. In materials science “particle” is a general term to describe small solid objects with sizes ranging from atomic scale (10−10 m) to the microscopic scale (10−3 m). However, the particle size often lies between 10−9-10−5 m. Large particles (>10−6) are commonly called grains (i. e. zeolites, carbon, Raney metals) and small particles (<15 nm) are frequently added (metals) to mixed oxides, i.e. TiO2—SiO2, SiO2 or TiO2. All materials consist of grains (particles) formed by the agglomeration of nanoparticles.
In conventional materials the grains have a size ranging from 100 micrometers to millimeters (mm), while the Nanomaterials particles are in the order of a one billionth of a meter (10−9). A nanometer is around the average diameter of human hair. The radius of an atom is 1 to 3 Angstrom (Å) and a nanometer is equal to 10 Å. Nanomaterials are rigid solid, resistant and are ductile at high temperatures, are resistant to degradation, erosion and corrosion, are also very chemically active. The physical and chemical properties of each nanomaterial or nanostructured material are determined by the type of interactions compounds that functionalized the nanoparticles; as well the electronic density and hydroxyl concentration in the net have an important role in the DNA cracking.
One of the areas in which nanoparticles have increased the importance is in the field of catalysis and biocatálisis, in order to obtain a distribution of particles with well defined shape and size to improve the catalytic activity. In particular, it is necessary to obtain highly dispersed particles in which most of the atoms are located on the surface. The structure includes a solid area, pore size, as well as the shape and volume of the pores. These parameters are important in catalysis and in biocatalysis, because they are responsible to increase the reaction rate. Although the catalytic activity can be related directly with its total contact area between the material and the reactive to catalyze, the determination of the area is generally considered to be an important requirement in the characterization of the biocatalysts. Furthermore, it is necessary to specify the nature of the structure of the pores as they control the transport of reagents and products in the catalytic reaction. In many cases, the course of the reaction is influenced by the size and shape of the pore but the particle size of the support and the metals are more definitively.
Titanium dioxide occurs in nature in three crystalline phases; anatase, rutile and brookite. The anatase and brookite can transform into rutile at high temperatures. The anatase to rutile can be irreversibly transformed by heating. There are several factors that influence the phase shift, such as particle size, crystal morphology, but in particular influence of the poisoning ions to the network. The literature indicates that the three phases, the anatase has a great chemical stability, resistance to corrosion, is inert from biological agents and has high specific surface area. However, the commercial titania Is a mix (Degussa P25) and contains 60 to 80% anatase. The problem only to produce the anatase phase is due to the rutile phase is thermodynamically more stable. Therefore by the sol-gel process is possible to obtain pure anatase and pure rutile. The structure of anatase and rutile are tetragonal, whereas brookite is orthorhombic, each titanium atom is attached to 6 oxygen atoms almost equidistant and each oxygen atom is linked to three atoms of titanium Some antecedents of similar materials can be found in: WO 2006/080241, WO 2004/089839 as well as:
U.S. Pat. No. 6,124,367. This patent protects reservoirs used in the Fischer Tropsch reactions from sintering by imparting a higher degree of mechanical strength to the reservoir. It incorporates SiO2 and Al2O3 into the reservoir and claims a rutile-anatase ratio of 1/9. It is a porous reservoir with either a spherical or a cylindrical shape. It is made by extrusion, spray drying or tableting.
U.S. Pat. No. 6,117,814. This patent describes a titania reservoir which also incorporates silica and alumina as a binder into the structure. The purpose of the binder is to impart better mechanical properties to the reservoir. The size range of this reservoir is from between 20 to 120 microns. The reservoir is approximately 50% binder, which is fabricated by a sol-gel process.
U.S. Pat. No. 6,087,405. This patent describes a reservoir to be used in a Fischer Tropsch gas synthesis reaction. The reservoir incorporates group VII metals into its structure. The rutile-anatase ratio in the structure is a distinguishing feature of this patent.
WO2003/064324. The invention relates to a titanium oxide-based polymer composition. The inventive composition comprises a TiOx(OH)y(H2O)z(x+y+z=3) titanium oxide-based polymer in the form of a gel or sol. Said polymer, which has a one-dimensional (1D) structure, is made from concentrically-wound fibres having a periodicity, which is deduced from the spacing between said fibres, of between 3.5 Å and 4 Å. Each fibre comprises TiO6 octahedrons and each TiO6 octahedron shares two opposite edges with two adjacent octahedrons (2×2.92 Å) in order to form infinite chains which develop along the axis of a fibre.
According to the invention, two adjacent chains form double lines as a result of the shared edges (2×3.27 Å). The inventive polymer is suitable for use as a photosensitive element in a photovoltaic cell, such as a sunscreen for a window.
WO/2006/079757. Method of preparing stable oxide ceramic precursor sol-gel solutions based on lead, titanium, zirconium and lanthanide(s) and method of preparing said ceramic. The invention relates to a method of preparing a stable oxide ceramic precursor sol-gel solution based on lead, titanium, zirconium and lanthanide(s). The invention comprises the following successive steps consisting in: a) preparing a sol-gel solution by bringing a molecular lead precursor, a molecular titanium precursor, a molecular zirconium precursor and a molecular lanthanide precursor into contact with a medium comprising a diol solvent and optionally an aliphatic mono-alcohol; b) leaving the solution thus obtained to stand for a sufficient period of time in order to obtain a solution having an essentially-constant viscosity; and c) diluting the solution obtained in the preceding step with a diol solvent identical to that used in step a or a solvent that is miscible with said solvent, at a predetermined rate. The invention can be used to prepare an oxide ceramic material comprising lead, a lanthanide metal, titanium and zirconium.
WO2007/141590. Sol-gel nanostructured titania reservoirs for use in the controlled release of drugs in the central nervous system and method of synthesis. The invention is related to a sol-gel nanostructured titania reservoir and its synthesis which is biocompatible with brain tissue. The pore size distribution, crystallite size and the extent of the crystalline phase distribution of anatase, brookite and rutile can be fully controlled. This device may be used to contain neurological drugs. It may be inserted directly into brain tissue for the purpose of the controlled time release of drugs over a period of from 6 months to three years.
WO93/21969. Novel coating materials for biomedical applications, particularly for use on biomedical implants, the coating material containing gel-derived titania where the material is capable of inducing calcium phosphate formation onto its surface under in vitro conditions, e.g. in a simulated body fluid and/or under in vivo conditions, processes for the preparation of the coating materials as well as their use in biomedical implant technology.
These nanostructured products have thereby an innovative use and, in particular, provide the foundations of Catalytic Nanomedicine, to completely eliminate amputation and improve quality of life.
Formulations comprising a nanostructured particles consisting of a solid acid, made of mixed oxides of silica and titania (TiO2—SiO2); supporting in its dispersed matrix: copper, silver, gold, iron, rutenium, rhodium, cobalt, zinc, palladium, zinc, manganese, iridium and/or platinum metals at minimal concentrations, and at least one functionalizing agent in contact with the particle; for use as a surface, material and personal cleaner.
The present disclosure includes disclosure of a formulation, comprising a quantity of a silica oxide, a quantity of a titanium oxide, and a quantity (or quantities) of one or more of copper, silver, gold, iron, rutenium, palladium, zinc, manganese, iridium and/or platinum metals, as referenced herein.
The sol-gel methodology is used to control the physico-chemical properties of the material in a thin, nanometric size and with a wide surface area. The nanoparticle comprised in the disclosed formulation is characterized by being a solid acid consisting of mixed oxides of silica and titania incorporating in its dispersed matrix, copper, silver, gold, iron, rutenium, palladium, zinc, manganese, iridium and/or platinum metals, or mixtures thereof, to minimum concentrations; and at least one functionalizing agent in contact with the particle. The carrier may be in liquid, oil, gel or solid form.
The functionalizing agent may have several functions. One function is stabilizing the particle in a carrier so that particles do not agglomerate and are uniformly distributed. In addition it may also assist in releasing antimicrobially effective amounts of ions into the environment of a microbe. The functionalizing agents may include polyurethanes and water soluble polymers, they promote dissolution in paints, and also improves adherence to the microbial surfaces. Functionalization agents may also include hydrophobic polymers which are used as emulsions and solutions to modify the particulate surfaces.
The formulation that comprises the nanostructured particles is effective as a broad-spectrum, fast-acting antimicrobial agent. The antimicrobial effectiveness of the functionalized nanoparticles has been evaluated using standard methods which resulted hi a significant effect in the killing of different types of microbes including bacteria, viruses, molds and fungi.
The present product can be formulated, depending on the carrier, as a surface cleaner, directed to be applied on any type of surface to eliminate microbial agents and prevent infections. The product can be further formulated as a material cleaner, directed to be applied to any type of material to eliminate microbial agents and prevent infections. Furthermore, the product can be formulated as a personal hygiene product to be applied on the skin, hair, nails and other external tissues to eliminate microbial agents and prevent infections.
The use of the product is of particular interest, but not limited to the sanitization of surfaces and materials in hospitals, clinics and other health institutions for decreasing transmission of nosocomial infections.
Sol-gel process using metal alkoxides.
At the functional group level, three reactions are generally used to describe the sol-gel process: hydrolysis, alcohol condensation, and water condensation. However, the characteristics and properties of a particular sol-gel inorganic network are related to a number of factors that affect the rate of hydrolysis and condensation reactions, such as, pH, temperature and time of reaction, reagent concentrations, catalyst nature and concentration, H2O/M molar ratio (R), aging temperature and time, and drying. Of the factors listed above, pH, nature and concentration of catalyst, H2O/M molar ratio (R), and temperature have been identified as most important. Thus, by controlling these factors, it is possible to vary the structure and properties of the sol-gel-derived inorganic network over wide ranges. For example, Sakka et al. observed that the hydrolysis of TEOS utilizing R values of 1-2 and 0.01 M HCl as a catalyst yields a viscous, spinnable solution. It was further shown, that these solutions exhibited a strong concentration dependence on the intrinsic viscosity and a power law dependence of the reduced viscosity on the number average molecular weight(31-34):
[n]=k(Mn)a (1)
Values for a ranged from 0.5 to 1.0, which indicates a linear or lightly branched molecule or chain.
Values of “a” in eq. 1 ranged from 0.1 to 0.5, indicating spherical or disk shaped particles. These results are consistent with the structures which emerge under the conditions employed by the Ströber process, for preparing SiO2 powders. It was further shown that with hydrolysis under basic conditions and R values ranging from seven (7) to twenty-five (25), monodisperse, spherical particles could be produced.
Generally speaking, the hydrolysis reaction (Eq. 2), through the addition of water, replaces alkoxide groups (OR) with hydroxyl groups (OH). Subsequent condensation reactions are made, involving the silanol groups (Si—OH) produce siloxane bonds (Si—O—Si) plus the by-products water or alcohol in the case of silica. Under most conditions, condensation commences before hydrolysis is complete. However, conditions such as, pH, H2O/Si molar ratio (R), and catalyst can force completion of hydrolysis before condensation begins. Additionally, because water and alkoxides are immiscible, a mutual solvent is utilized. With the presence of this homogenizing agent, alcohol, hydrolysis is facilitated due to the miscibility of the alkoxide and water. As the number of siloxane bonds increases, the individual molecules are bridged and jointly aggregate in the sol. When the sol particles are aggregate, or inter-knit into a network, a gel is formed. Upon drying, trapped volatiles (water, alcohol, etc.) are driven off and the network shrinks as further condensation can occur. It should be emphasized, however, that the addition of solvents and certain reaction conditions may promote esterification and depolymerization reactions. The hydrolysis/condensation reaction follows two different mechanisms, which depend of the coordination of metallic central atom. When the coordination number is satisfied the hydrolysis reaction occurs by nucleophilic substitution (Se):
Hydrolysis reaction via nucleophilic substitution (Sn).
When the coordination number is major, the hydrolysis reaction takes place by nucleophilic addition:
Hydrolysis reaction via nucleophilic addition (An).
These mechanisms need that the oxygen coordination is increased from 2 to 3, the additional bond generation involves one electron pair of the oxygen and the new bond can be equivalent to the other bonds. During the condensation step an enormous concentration of hydroxyl groups are formed. This OH can be linked between the metallic atoms or only be simple —OH ligand in the surface.
Under acidic conditions, it is likely that an alkoxide group is protonated in a rapid first step. Electron density is withdrawn from the silicon atom, making it more electrophilic and thus more susceptible to attack from water. This results in the formation of a penta-coordinate transition state with significant SN2-type character. 13 The transition state decays by displacement of an alcohol and inversion of the silicon tetrahedron, using silica as example:
Base-catalyzed hydrolysis of silicon alkoxides proceeds much more slowly than acid-catalyzed hydrolysis at an equivalent catalyst concentration. Basic alkoxide oxygens tend to repel the nucleophile, —OH. However, once an initial hydrolysis has occurred, following reactions proceed stepwise, with each subsequent alkoxide group more easily removed from the monomer then the previous one. Therefore, more highly hydrolyzed silicones are more prone to attack. Additionally, hydrolysis of the forming polymer is more sterically hindered than the hydrolysis of a monomer. Although hydrolysis in alkaline environments is slow, it still tends to be complete and irreversible. Thus, under basic conditions, it is likely that water dissociates to produce hydroxyl anions in a rapid first step. The hydroxyl anion then attacks the silicon atom. Again, an SN2-type mechanism has been proposed in which the —OH displaces —OR with inversion of the silicon tetrahedron.
1.6871 g Of acetil platinum acetonate (Pt(acac)2) were mixed with 246 ml of acetone. The mixture was maintained under agitation until the platinum complex was dissolved. To this mixture, 1.2501 g of GABA previously dissolved in 20 ml of deionized water was added. pH was adjusted to 3 with phosphoric acid. Simultaneously, 89 ml of TEOS and 9.8 ml of titanium butoxide dissolved in 70 ml of deionized water were added. Everything was maintained under agitation and at room temperature until de gel was formed.
1.6871 g Of acetil platinum acetonate (Pt(acac)2) were mixed with 246 ml of acetone. The mixture was maintained under agitation until the platinum complex was dissolved. To this mixture, 1.2501 g of glutamic acid previously dissolved in 20 ml of deionized water was added. pH was adjusted to 3 with phosphoric acid. Simultaneously, 89 ml of TEOS and 9.8 ml of titanium butoxide dissolved in 15 ml of absolute ethanol. 1.7203 g of ammonium sulphate dissolved in 70 ml of deionized water was added. Everything was maintained under agitation and at room temperature until de gel was formed.
1.6871 g Of acetil platinum acetonate (Pt(acac)2) were mixed with 246 ml of acetone. The mixture was maintained under agitation until the platinum complex was dissolved. To this mixture, 1.2501 g of GABA previously dissolved in 40 ml of deionized water was added. pH was adjusted to 3 with phosphoric acid. Simultaneously, 89 ml of TEOS and 9.8 ml of titanium butoxide dissolved in 15 ml of absolute ethanol were added. 1.7203 g of ammonium sulphate dissolved in 140 ml of deionized water was added. Everything was maintained under agitation and at room temperature until de gel was formed.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2018/055337 | 7/18/2018 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62534751 | Jul 2017 | US |
