NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMERS, OBTENTION METHOD, AND USE

Abstract

Method for obtaining a material containing nanostructured reactive molecules based on niobium compounds, the products obtained, and the use thereof as a chemical/biological barrier on surfaces. The nanostructured hybrid material can be used as a component in cosmetic products, intensifying the efficiency and action time thereof. Furthermore, the material can be incorporated into different surfaces, including fabric, retaining its anti-bacterial and anti-viral properties. The material can also be applied in the form of a gel or liquid spray. The niobium nanoparticles combined with quaternary ammonium compounds for sprays and with methylene blue colour to form sanitizing gels are highly efficient in deactivating coronavirus, with prolonged stability and activity.

Claims

1. NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMERS, comprising negatively charged niobium oligomers and organic cations, selected from quaternary ammonium salts of the didecyldimethylammonium chloride, hexadecyltrimethylammonium bromide (CTAB), methylene blue, gentian violet or fuchsine dye, at concentrations of 10 to 2000 mg/L of quaternary ammonium for concentrations between 100 and 3000 mg/L of niobium.

2. NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMERS, according to claim 1, wherein the negatively charged niobium oligomers are obtained from niobium oxides, niobium pentoxide, niobic acid and niobium phosphate, according to a processing comprising: a) dissolving the niobium compounds, containing between 1 and 5 g/L of niobium, in oxalic acid or hydrogen peroxide, in concentrations between 10 and 50% m/m; b) adding 10 to 1000 mg/L of quaternary ammonium salt and/or 500 to 20,000 mg/L of cationic dye to the niobium oligomer obtained in step a); c) stirring the solution obtained in step b) between 10 and 100 rpm, for a period of time between 5 and 30 min, at room temperature the pr ccss defined in claim 5.

3. NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMERS, according to claim 1, wherein the nanostructured hybrid material is incorporated into alcohol gel between 10 and 70% m/m, in ratios of 0.1 to 10% by mass of the niobium compound.

4. A METHOD OF OBTAINING THE NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMERS, defined in claim 1, comprising the following steps: a. dissolving the niobium compounds, containing between 1 and 5 g/L of niobium, in oxalic acid or hydrogen peroxide, in concentrations between 10 and 50% m/m; b. Aadding 10 to 1000 mg/L of quaternary ammonium salt and/or 500 to 20,000 mg/L of cationic dye to the niobium oligomer obtained in step a); c. stirring the solution obtained in step b) between 10 and 100 rpm, for a period of time between 5 and 30 min, at room temperature.

5. THE METHOD OF OBTAINING A NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMER, according to claim 4, wherein in step a) the niobium compounds are selected from the group consisting of niobium oxides, niobium pentoxide, niobic acid and niobium phosphate.

6. THE METHOD OF OBTAINING A NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMERS, according to claim 4, wherein in step b) the quaternary ammonium is selected from didecyldimethylammonium chloride or hexadecyltrimethylammonium bromide (CTAB).

7. THE METHOD OF OBTAINING A NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMERS, according to claim 4, wherein in step b) the cationic dye is selected from the group comprising dye methylene blue, gentian violet or fuchsine.

8. THE METHOD OF OBTAINING A NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMERS, according to claim 4, wherein 0.1 to 5% m/m of alcohol gel 10 to 70% m/m is added after step c).

9. A method of producing sanitizing compounds, with bactericidal and antiviral activities comprising using the nanostructured hybrid material based on niobium oligomers according to claim 1.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0011] FIG. 1 shows a photograph with the products in gel and liquid (B) form from niobium oxide.

[0012] FIG. 2 shows the CTAB NMR spectra, of the new Nb-CTAB molecule and of the model created for the protection generated with the application on surfaces (B).

[0013] FIG. 3 shows the feasibility study of Enterococcusfaecalis (Ef), Escherichia coli (Ec) and Eikenellacorrodens (Ek) bacteria using niobium compounds (A=niobium spray/CTAB; B=niobium spray/CTAB/methylene blue; C=niobium gel/methylene blue).

[0014] FIG. 4 shows the viral load reduction studies for the different samples and their respective controls. In (A), the control samples for the spray are represented by s1-s12 and s13 and the control samples for the gel are represented by g1 and g2, g4-g6. (B) and (C) show the study of the prolonged viral load reduction effect of liquid and gel materials (S12=niobium spray/CTAB; g3=niobium spray/CTAB/methylene blue; g7=niobium gel/methylene blue). The red arrow indicates the result for the g7 sample, which inactivated all the viruses.

DETAILED DESCRIPTION OF THE TECHNOLOGY

[0015] The present technology describes the process of obtaining a material containing nanostructured reactive molecules based on niobium compounds, the products obtained and their use as a chemical/biological barrier on surfaces. The nanostructured hybrid material can be used as a component of cosmetic products, intensifying its effectiveness and time of action. In addition, it can be incorporated into different surfaces, including fabrics, maintaining its action against bacteria and viruses. It can also be applied in the form of a gel or liquid spray. Niobium nanoparticles combined with quaternary ammonium compounds for sprays and with methylene blue dye to form sanitizing gels showed high efficiency in deactivating the coronavirus, with stability and prolonged activity.

[0016] The niobium oligomer-based nanostructured hybrid material contains negatively charged niobium oligomers and organic cations selected from the group comprising quaternary ammonium salts of the didecyldimethylammonium chloride type, hexadecyltrimethylammonium bromide (CTAB), methylene blue, gentian violet and/or fuchsine dye, at concentrations of 10 to 2000 mg/L of quaternary ammonium for concentrations between 100 and 3000 mg/L of niobium.

[0017] Negatively charged niobium oligomers can be obtained from niobium oxides, niobium pentoxide, niobic acid and niobium phosphate.

[0018] The nanostructured hybrid material based on niobium oligomers can be incorporated into alcohol gel between 10 and 70% m/m, in proportions of 0.1 to 10% by mass of the niobium compound.

[0019] The process for obtaining the nanostructured hybrid material based on niobium oligomers comprises the following steps:

a. Dissolving the niobium compounds, containing between 1 and 5 g/L of niobium, in oxalic acid or hydrogen peroxide, in concentrations between 10 and 50% m/m; [0020] b. Adding 10 to 1000 mg/L of quaternary ammonium salt and/or 500 to 20,000 mg/L of cationic dye to the niobium oligomer obtained in step “a”; [0021] c. Stirring the solution obtained in step “b” between 10 and 100 rpm, for a period of time between 5 and 30 min, at room temperature.

[0022] The niobium compounds described in step “a” are selected from the group comprising their oxides, being niobium oxides, niobium pentoxide, niobic acid and niobium phosphate.

[0023] The quaternary ammonium, described in step “b”, is selected from the group comprising didecyldimethylammonium chloride or hexadecyltrimethylammonium bromide (CTAB) and the cationic dye is selected from the group comprising methylene blue, gentian violet or fuchsine dye, which may be added 0.1 to 5% m/m of alcohol gel 10 to 70% m/m after step “c”.

[0024] The nanostructured hybrid material based on niobium oligomer can be used in the production of sanitizing compounds, with bactericidal and antiviral activities, preferably against coronaviruses.

[0025] The following examples describe aspects of the present technology and should not be considered as limiting.

EXAMPLE 1—OBTAINING AND USING A NANOSTRUCTURED HYBRID MATERIAL BASED ON NIOBIUM OLIGOMER FOR THE DEACTIVATION OF THE CORONAVIRUS

[0026] The compounds in spray form are obtained by the reaction of the niobium oligomer containing 2,000 mg/L of niobium with the quaternary ammonium (CTAB) 100 mg/L. CTAB is dripped into the oligomer solution until the formation of a micelle containing niobium and CTAB chemically bonded to form Nb-CTAB. It is important to point out that the micellar point is obtained before the solution gelling, so that agitation must be observed and the medium gelling should be avoided. The resulting micelle should be kept under gentle agitation at 100 rpm for 10 min.

[0027] The sanitizing gel was obtained from the reaction of the methylene blue dye and the niobium compound using equal volumes of the compounds, the dye concentration being 1000 mg/L and the niobium compound concentration of 2,000 mg/L. This material has good sanitizing properties, especially when associated with alcohol gel 70% m/m. In the mixture with alcohol gel 70% m/m, a ratio of 0.5% by mass of the sanitizing gel formed by Nb-methylene blue was prepared.

[0028] FIG. 1 shows a photograph of the final gel obtained containing 0.5% methylene blue dye in 70% alcohol gel and sprays containing 10 mg/L of CTAB quaternary ammonium in aqueous niobium compound.

[0029] Strong evidence of the chemical interaction established between the negatively charged species of niobium and CTAB was obtained by RAMAN spectroscopy, where the shifts referring to the established chemical interactions are clearly observed, as shown in FIG. 2a. A model of the newly formed structure and its effect on the skin surface as a protective layer is presented in FIG. 2b. Thus, based on the analysis of the .sup.1H NMR spectra for the surfactant CTAB and the mixture containing the niobium compound and CTAB, both in D.sub.2O, it can be inferred that there is an interaction between the species, and this synergism potentiates the activity of sample against the virus that causes COVID-19. The niobium compound has a high negative surface charge, which, when interacting with the positive part of the surfactant, transfers electron density, making the hydrogens of the molecule more shielded, causing a significant difference between the chemical shifts of the H. The hydrogens of the methyl groups of CTAB present a chemical shift (5) of 3.16 ppm, however, when interacting with Nb, it is observed a shift to δ=4.31 ppm, which due to the strong influence of the metal, presents itself as an extended singlet and practically superimposed on the water signal. Ha, the carbon hydrogen directly bonded to the N atom of CTAB, has a δ=3.41 ppm; however, in the presence of Nb, the triplet corresponding to this H undergoes a shift to δ=2.91 ppm. The chemical shifts of the compounds clearly indicate the formation of a new chemical species established between Nb-CTAB.

EXAMPLE 2—BACTERIA DEACTIVATION STUDY

[0030] The products were tested in the feasibility study of Enterococcusfaecalis (Ef), Escherichia coli (Ec) and Eikenellacorrodens (Ek) bacteria. For the studies, 100 μL of BHI culture medium and 100 μL of sterile distilled water were added to each well of the culture medium sterility control plate. The microplates are incubated in an oven at 37° C. and after 24 h the first test reading is performed in a microplate reader. After 48 h, a new reading should be performed, ending the test. Readings are taken at a fixed wavelength of 492 nm. The studies in FIG. 3 showed the ability of the materials to promote the deactivation of three types of bacteria. In the studies carried out, 1.0×0.5 cm silver plates were sequentially polished on 1500, 2000 and 2500 mesh SiC sandpaper and with commercial polishing paste before the cleaning baths. This procedure is optional and not recommended for objects that have details, such as texts and images, on their surfaces.

EXAMPLE 3—STUDY OF VIRAL LOAD REDUCTION

[0031] For viral load reduction studies directly employing the coronavirus, eight parts of the compound were adapted to room temperature (RT) and mixed with one part of the virus suspension. Immediately after incubation for defined periods at room temperature, the mixture was diluted 1:10. After four days of incubation at 37° C. in a CO.sub.2 incubator, cells were microscopically examined for virus-specific cytopathogenic effects after 10 min of virus contact with the niobium compound. All tests were performed in triplicate.

[0032] Initially, exploratory studies were carried out with different proportions of the compounds and with the materials separately. FIG. 4(A) presents these data and clearly shows the potentiated effect of the new molecule formed by the reaction between the niobium compound and CTAB. In fact, the results of samples S10 (representing a solution containing pure CTAB dissolved in water) and S12 (sample containing the same content of CTAB reacted with niobium), clearly indicate the potentiated effect of the Nb-CTAB species.

[0033] Only CTAB promoted a viral load reduction of approximately 30%, while the new molecule Nb-CTAB promoted a 90% reduction in viral load. This result clearly shows the potentiation of the action of the new hybrid molecule formed by the reaction between CTAB and the negatively charged species of niobium, according to the model generated in the present technology.

[0034] Another result that deserves to be highlighted is the data referring to the combination of niobium gel containing niobium-methylene blue with alcohol gel. The presence of niobium gel promoted a viral load reduction of 100%, according to the results of the g7 sample in FIG. 4(A). In turn, alcohol gel (sample g1) without the presence of the Nb-methylene blue compound showed a viral load reduction of only 15%.

[0035] FIG. 4 also presents two ways of presenting the assessment of viral load reduction using the niobium hybrid products developed in the present technology. Graph B indicates that, for values below 1, viral load reduction was observed in the presence of niobium compounds. Graph C shows the same result, but in a quantitative linear form. The results also show that the products have a prolonged effect because the materials were deposited on a glass surface and the virus deposited after 1, 4 and 24 hours. After this period on the surface, the virus was deposited and after 10 min the viral load was analyzed. The material marked as g7 in the graphs showed 100% removal of the virus at all times studied, indicating its efficiency and, in addition, its ability to remain active after 24 h after its application on the surface. The material marked g7 is niobium gel containing methylene blue chemically bonded to the niobium oligomer. As seen in FIG. 4(A), pure alcohol did not show high efficiency under the conditions of the experiments; however, the niobium compound continues to act in the deactivation of the coronavirus for a longer time and with more efficiency compared to pure commercial alcohol gel. The data show that in compounds containing niobium, only 0.5% of it dispersed in commercial alcohol gel promotes 100% reduction in viral load after 24 h of deposition on surfaces. These results indicate the efficiency of the new species formed between the niobium compound and the methylene blue dye, forming in an unprecedented way a semiconductor gel capable of photocatalytically acting in the deactivation of the coronavirus, allowing the formation of a material with the ability to act in a prolonged way on the different surfaces. It should be clear that pure alcohol loses its activity with natural evaporation, but that the niobium species remains active, making this new compound unique in the fight against coronavirus.

[0036] Materials g3 and S12, which are sprays containing the hybrid niobium compounds in liquid form, also showed the ability to deactivate the coronavirus, although less efficient when compared to material g7. These compounds in liquid form also showed efficiency with prolonged time, being active even after 6 h of deposition on surfaces.

[0037] The results obtained indicate that the materials described in the present invention have high potential to be used in the fight against coronavirus and can be used in the form of a spray as a sanitizer and in the form of gel and can be used as a component of an alcohol gel.