Niobium oxyhydroxide as a bioactive agent and reinforcement to a high-viscosity bulk-fill resin composite.

OBJECTIVE: The present in vitro study incorporated niobium oxyhydroxide fillers into an experimental high-viscosity bulk-fill resin composite to improve its mechanical performance and provide it a bioactive potential. METHODOLOGY: Scanning electron microscopy synthesized and characterized 0.5% niobium oxyhydroxide fillers, demonstrating a homogeneous morphology that represented a reinforcement for the feature. Fillers were weighed, gradually added to the experimental resin composite, and homogenized for one minute, forming three groups: BF (experimental high-viscosity bulk-fill resin composite; control), BF0.5 (experimental high-viscosity bulk-fill resin composite modified with 0.5% niobium oxyhydroxide fillers), and BFC (commercial bulk-fill resin composite Beautifil Bulk U, Shofu; positive control). In total, 10 specimens/groups (8 × 2 × 2 mm) underwent flexural strength (FS) tests in a universal testing machine (Instron) (500N). Resin composites were also assessed for Knoop hardness (KH), depth of cure (DoC), degree of conversion (DC), elastic modulus (E), and degree of color change (ΔE). The bioactive potential of the developed resin composite was evaluated after immersing the specimens into a simulated body fluid in vitro solution and assessing them using a Fourier-transformed infrared spectroscope with an attenuated total reflectance accessory. One-way ANOVA, followed by the Tukey's test (p<0.05), determined FS, DC, KH, and ΔE. For DoC, ANOVA was performed, which demonstrated no significant difference between groups (p<0.05). CONCLUSIONS: The high-viscosity bulk-fill resin composite with 0.5% niobium oxyhydroxide fillers showed promising outcomes as reinforcement agents and performed well for bioactive potential, although less predictable than the commercial resin composite with Giomer technology.

Sol-gel and Pechini niobium modified: synthesis, characterization and application in the 2,4-D herbicide degradation.

In this work, a comparison was made between the synthesis of niobium-based materials (Nb2O5), both in terms of material characterization and catalytic performance. The methods used were chemical mixtures: modified sol-gel and Pechini. The materials were calcined at different temperatures (753, 873 and 993K) and characterized by the following techniques: photoacousticspectroscopy (PAS), zero charge point (pHPZC), scanning electron microscopy (SEM/EDS), thermogravimetric analysis (TGA/DTG) and X-ray diffraction (XRD). The photocatalytic process was carried out to evaluate the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) under UV radiation (250 W mercury vapor lamp) and different experimental conditions. In addition, to better understand the influence of parameters such as pH, catalyst concentration (0.2, 0.5 and 0.8 g L-1) and calcination temperature, a Design of Experiments (DoE) was used. The results indicated that despite having similar structures and phases in the XRD analysis, the morphology presents two distinct surfaces, due to the preparation method. Differences in the synthesis method affected the catalytic activity in the parameters studied. Although the zero charge point values are close (6.18-6.36), we observed differences in the band gap depending on the calcination temperature. In the optimal condition studied, the catalyst prepared by the sol-gel method obtained the best results.

Remineralizing potential of a fluoride varnish modified by bioactive nanoparticles / Potencial remineralizante de um verniz fluoretado modificado por nanopartículas bioativas

Objective: Evaluate a fluoride varnish modified by nanostructures with the bioactive qualities of silica (SiO2) and niobium pentoxide (Nb2O5), testing its remineralizing potential by surface hardness (SH) and energy-dispersive X-ray spectroscopy (EDX). Material and Methods: Bovine enamel specimens (6×4×2mm) were prepared and submitted to a demineralizing/remineralizing process to produce a subsurface caries-like lesion, evaluated by transversal microradiography image (TMR) and subsequently distributed randomly into three groups: fluoride varnish (VZ); fluoride varnish + silica gelatin (VZ-SiO2) and fluoride varnish + niobium nanoparticles (VZ-Nb2O5). The specimens were subjected to a pH-cycling demineralizing/remineralizing process for 7 days at 37ºC. The %SH loss and %SH recovery (after the pH-cycling regimen) were calculated (n=10/group). The Ca/P weight ratio before and after the pH-cycling regimen was evaluated through SEM/EDX. A two-way ANOVA followed by Tukey's test (p<0.05) was performed for hardness and EDX. Results: TMR image showed the formation of an artificial subsurface lesion, and a significant SH increase was observed in the VZ-Nb2O5 group (p<0.05). Regarding the %SHL and %SHR, the VZ-Nb2O5 and VZ-SiO2 were significantly different compared to the VZ group (p<0.001), but VZ-Nb2O5 presented higher values. The Ca/P ratio showed that blocks treated with VZ-SiO2 and VZ-Nb2O5 showed greater ion deposition, particularly in the presence of Nb. Conclusion: The bioactivity of niobium facilitated greater interaction between the enamel and the varnish, leading to a slow release of nanoparticles and a longer-lasting remineralizing effect (AU)

Objetivo: Avaliar um verniz fluoretado modificado por nanoestruturas com a bioatividade da sílica (SiO2) e pentóxido de nióbio (Nb2O5), testando seu potencial remineralizador pela dureza de superfície (SH) e espectroscopia de energia dispersiva de raios-X (EDX). Material e Métodos: Espécimes de esmalte bovino (6×4×2mm) foram preparados e submetidos à desmineralização/remineralização para produzir uma lesão subsuperficial semelhante a cárie, avaliada por imagem de microrradiografia transversal (TMR) sendo distribuída em três grupos: verniz fluoretado (VZ); verniz fluoretado+gelatina de sílica (VZ-SiO2) e verniz fluoretado+nanopartículas de nióbio (VZ-Nb2O5). As amostras foram submetidas à desmineralização/remineralização por ciclagem de pH durante 7 dias a 37°C. A porcentagem de perda e recuperação de SH foram calculadas (n=10/grupo). A relação em peso Ca/P antes e depois da ciclagem foi avaliada através de MEV/EDX. ANOVA a dois critérios seguida do teste de Tukey (p<0,05) foi realizada para dureza e EDX. Resultados: A TMR mostrou a formação de uma lesão subsuperficial e um aumento significativo de SH foi observado no grupo VZ-Nb2O5 (p<0,05). Em relação ao %SHL e %SHR, o VZ-Nb2O5 e o VZ-SiO2 foram significativamente diferentes em relação ao grupo VZ (p<0,001), mas o VZ-Nb2O5 apresentou valores maiores. A relação Ca/P mostrou que os blocos tratados com VZ-SiO2 e VZ-Nb2O5 apresentaram maior deposição de íons, principalmente na presença de Nb. Conclusão: A bioatividade do nióbio facilitou maior interação entre o esmalte e o verniz, levando a uma liberação lenta de nanopartículas e a um efeito remineralizante mais duradouro (AU)

Mechanical and antibacterial properties of an experimental flowable composite containing Nb2O5 and NF_TiO2 nanoparticles.

This study developed an experimental flowable composite incorporated with niobium pentoxide (Nb2O5) combined or not with titanium dioxide co-doped with fluorine and nitrogen (NF_TiO2) and evaluated the mechanical and antibacterial properties. The experimental flowable composite (TEGDMA + BisGMA 1:1 + 60%wt - inorganic filler - borosilicate 0.7 µm) was formulated according to the type and concentration of Nb2O5 and NF_TiO2 (0.5, 1, 1.5 and 2 wt%) or NF_TiO2 + Nb2O5 (0.25, 0.5, 0.75 and 1 wt% - 1:1). The control groups were formed by the experimental composite without the incorporation of Nb2O5 and/or NF_TiO2 (GC-E) and by a commercial flowable composite (GC). The characterization of the surface of the composite and its particles was carried out using scanning electron microscopy (SEM) and energy dispersive x-rays (EDX). Specimens were manufactured and subjected to mechanical tests of flexural strength (FS) (n = 12), flexural modulus (FM) (n = 12), roughness (Ra) (n = 10), microhardness (n = 10), and contact angle (n = 10); and, to evaluate the antibacterial activity, they were submitted to tests of biofilm formation against S. mutans (CFU/mL) (n = 5), biofilm biomass by dry weight (n = 5) and confocal laser microscopy (%LIVE/DEAD) (n = 5). Data were submitted to one-way ANOVA and Tukey's post-hoc and, those that were not homoscedastic, but with normality, were submitted to Welch's ANOVA and Games-Howell's post-hoc. Dunnet's test was used to compare the controls with the other experimental groups (α = 5). The Nb2O5 particles had an average size of 32.4 µm and the nanoparticles (NPs) of NF_TiO2, 10 nm. EDX analysis identified isolated peaks of N, F, Ti, and Nb confirming the presence of these particles in the resin matrix. The 1.5% NF_TiO2 group had a higher FS and FM than the controls (p < 0.05). GC showed higher microhardness between groups (p < 0.05). There was no difference between the experimental groups regarding contact angle and roughness (p > 0.05), except for GC, which had the highest Ra values and the lowest contact angle between groups (p < 0.05). Composites containing 0.5%, 1%, 1.5%, and 2% Nb2O5, 1%, 1.5%, and 2% NF_TiO2 and 2% Nb2O5 + NF_TiO2 showed lower biofilm formation (p < 0.05), lower total biofilm biomass (p < 0.05), and a higher percentage of dead cells (44%, 52%, 52%, 79%, 42% 43%, 62%, 65%, respectively) than GC and GC-E (5% and 1%, respectively). It is concluded that the incorporation of 1.5% NF_TiO2 promoted a greater FS and FM among the experimental composites and that the addition of Nb2O5 particles (0.5%, 1%, 1.5%, and 2%), NF_TiO2 (1%, 1.5% and 2%) and the combination Nb2O5 + NF_TiO2 (2%) showed significant antibacterial effects.

Using rice husk ash as a SiO2 source in the preparation of SiO2/Nb2O5 and SiO2/ZnS heterostructures for photocatalytic application.

This work presents the synthesis of SiO2/Nb2O5 and SiO2/ZnS heterostructures using the microwave-assisted hydrothermal (MAH) method, which is fast and has low temperature. The silica used in the synthesis was obtained by burning the rice husk without any pre- or post-treatments. The obtained samples were characterized using various techniques such as X-ray diffraction (XRD), energy-dispersive X-ray analysis (EDX), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), and UV-visible. The obtained silica was found to be amorphous, and the materials used for modification showed characteristic of the type of synthesis used. SEM images showed that Nb2O5 and ZnS interacted with the SiO2 surface, filling the voids. In the photocatalytic process, the heterostructures showed enhanced decolorization efficiency for dyes such as rhodamine B (RhB) and methylene blue (MB) compared to SiO2. For RhB, the silica decolorized approximately 24%, and for MB, it discolored approximately 27%; SiO2/Nb2O5 showed 91.24% decolorization efficiency for RhB and 72.77% MB, while SiO2/ZnS showed approximately 96% for RhB and 100% for MB. All samples were tested under the same conditions. This demonstrates that the use of rice husk residue not only improves the photocatalytic activity of heterostructures but also promotes the utilization of improperly discarded residues.

Niobium: The Focus on Catalytic Application in the Conversion of Biomass and Biomass Derivatives.

The world scenario regarding consumption and demand for products based on fossil fuels has demonstrated the imperative need to develop new technologies capable of using renewable resources. In this context, the use of biomass to obtain chemical intermediates and fuels has emerged as an important area of research in recent years, since it is a renewable source of carbon in great abundance. It has the benefit of not contributing to the additional emission of greenhouse gases since the CO2 released during the energy conversion process is consumed by it through photosynthesis. In the presented review, the authors provide an update of the literature in the field of biomass transformation with the use of niobium-containing catalysts, emphasizing the versatility of niobium compounds for the conversion of different types of biomass.

Niobium-containing bioactive glasses modulate alkaline phosphatase activity during bone repair.

This study aimed to evaluate the pre-clinical behavior of niobium-containing bioactive glasses (BAGNb) by their ability to promote bone repair and regulate alkaline phosphatase (ALP) levels in an animal model. BAGNbs were produced as powders and as scaffolds and surgically implanted in the femur of male rats (Wistar lineage n = 10). Glasses without Nb (BAG) were produced and implanted as well. The Autogenous Bone (AB) was used as a control. After 15, 30, and 60 days of surgical implantation, blood serum samples were collected to quantify ALP activity, and femurs were removed to assess bone repair. Bone samples were histologically processed and stained with H&E to quantify the % new bone into defects. No postoperative complications were identified. Early-stage repair (15 days) resulted in increased ALP activity for all groups, with increased values ​​for powdered BAGNb. The maturation of the new bone led to a reduction in serum ALP levels. Histological sections showed the formation of immature bone tissue and vascularization with the progression of bone deposition to mature and functional tissue over time. BAG powder showed less new bone formation in 15 days, while the analysis at 30 and 60 days showed no difference between groups (p > .05). Niobium-containing bioactive glasses safely and successfully induced bone repair in vivo. The modulation of ALP activity may be a pathway to describe the ability of niobium-containing materials to contribute to new bone formation.

Bleaching effectiveness and cytotoxicity of new experimental formulation of niobium-based bleaching gel.

OBJECTIVES: The development of new bleaching agents with minimum concentration of hydrogen peroxide (HP), without adverse effects, and with bleaching effectiveness, has great clinical relevance. The aim of this study was to evaluate the bleaching efficacy and cytotoxicity of a new niobium-based bleaching gel, compared to already available HP-based gels. MATERIALS AND METHODS: For the bleaching efficacy analysis, 40 bovine incisors were randomly divided into 4 groups according to the established bleaching protocol: control, untreated; 35HP, 35% HP bleaching gel; 6HP, 6% HP bleaching gel; NbHP, niobium gel associated with 3% HP gel. The color variation was measured in a spectrophotometer and the values of ΔL, Δa, Δb, and ΔE obtained. For the cell viability assay by MTT, MC3T3 cells were exposed to bleaching gel extracts (1:500, 1:250, 1:125 dilutions; immediately and 24 h). Statistical tests were performed (P < 0.05). RESULTS: The color alteration for all bleaching gels was significant compared to control (P < 0.05), but the NbHP gel showed a significant ΔE than other gels, with expressive color alteration at 14 days (P < 0.05). The 35HP showed high cytotoxicity regarding control and the most groups in all periods and extracts analyzed (P < 0.05), while the NbHP showed greater cell viability than control in the immediate period, dilution of the 1:500 and superior to 6HP in the most extracts at 24 h. CONCLUSION: The new experimental niobium-based gel has bleaching efficacy similar to that of gels with a high concentration of HP, and it has high cytocompatibility. CLINICAL RELEVANCE: The use of this new generation of niobium-based whitening gel associated with a low concentration of hydrogen peroxide represents the possibility of a tooth whitening with lower dentin sensitivity.

Orthodontic resins loaded with niobium silicate particles: Impact of filler concentration on the physicochemical and biological properties.

OBJECTIVES: White spot lesions (WSL) are prevalent in patients using orthodontic appliances. The presence of ion-releasing compounds in the tooth-appliance interface may limit enamel demineralization to control WSL incidence. Thus, this study aims to evaluate the mineral formation on SiNb-containing experimental orthodontic resins and the influence of these fillers on the physicochemical and biological properties of developed materials. MATERIALS AND METHODS: The SiNb particles were synthesized via the sol-gel route and characterized by their molecular structure and morphology. Photopolymerizable orthodontic resins were produced with a 75 wt% Bis-GMA/25 wt% TEGDMA and 10 wt%, 20 wt%, or 30 wt% addition of SiNb. A control group was formulated without SiNb. These resins were tested for their degree of conversion, softening in solvent, cytotoxicity in fibroblasts, flexural strength, shear bond strength (SBS), and mineral deposition. RESULTS: The addition of 10 wt% of SiNb did not impair the conversion of monomers, cytotoxicity, and flexural strength. All groups with SiNb addition presented similar softening in solvent. The presence of these particles did not affect the bond strength between metallic brackets and enamel, with SBS values ranging from 16.41 to 18.66 MPa. The mineral deposition was observed for all groups. CONCLUSION: The use of niobium silicate as filler particles in resins may be a strategy for the adhesion of orthodontic appliances. The 10 wt% SiNb concentration resulted in a material with suitable physicochemical and biological properties while maintaining the bond strength to tooth enamel and promoting mineral deposition.

Cu/Nb2O5, Fe/Nb2O5 and Cu-Fe/Nb2O5 applied in salicylic acid degradation: Parameters studies and photocatalytic activity.

This study describes the synthesis of Cu/Nb2O5, Fe/Nb2O5, and Cu-Fe/Nb2O5 catalysts obtained by incorporating copper and/or iron metals into niobium pentoxide (Nb2O5). The new materials were characterized by the following techniques: Thermogravimetric Analysis (TA), surface and pore analysis, X-ray diffractometry (XRD), and Fourier Transform Infrared Spectroscopy (FT-IR). The catalyst was applied in the photocatalytic degradation of salicylic acid (SA). The influence of different parameters (calcined temperature, pH, and metal addition) on the photocatalytic reaction was evaluated. The results indicated that catalysts containing copper were more active and pH influenced the SA degradation process. SA removal results indicated that Cu/Nb2O5 photocatalyst presented a 1.5 fold higher degradation after 120 min in comparison to Cu-Fe/Nb2O5 and 4.6 fold higher than Fe/Nb2O5 catalyst, all them calcined at 400 °C. In tests carried out in the presence of formic acid, increasing the pH from about 3 to 7 allowed an almost 3.4-fold increase in SA degradation for the Cu-Fe/Nb2O5 catalyst calcined at 400 °C.

Avaliação das propriedades físico-químicas e osteogênicas do cimento portland associado ao pentóxido de nióbio / Evaluation of the physicochemical and osteogenic properties of portland cement associated with niobium pentoxide

Este trabalho objetivou desenvolver, caracterizar e avaliar a atividade osteogênica de formulações de CP com diferentes proporções de óxido de Nióbio (Nb2O5), substituindo o Bi2O3. Foram utilizados três grupos, um controle e dois experimentais: GC (MTA Angelus®), F6 (75% CP, 20% Nb2O5 e 5% CaSO4) e F7 (75% CP, 10% Bi2O3, 10% Nb2O5e 5% CaSO4). As formulações foram submetidas às análises de Difração de RaioX (DRX), Microscopia Eletrônica de Varredura (MEV), Espectroscopia de Infravermelho com Transformada de Fourier (FTIR), Espectrometria de Fluorescência de Raios-X (FRX), pH, tempo de presa, radiopacidade, resistência a compressão, citotoxicidade e bioatividade. Os dados obtidos foram avaliados estatisticamente pelo teste de variância (ANOVA) com correção de Bonferroni (p<0,05%). O resultado do teste de pH: Nióbio 10% Imediato (12,205 ±0,304); 24h; (12,770 ± 0,226) 48h: (12,910 ± 0,169). Nióbio 20%: imediato (12,080 ± 0,282); 24 h: (12,350 ± 0,593); 48 h: (12,580 ± 0,73). Para o tempo de presa inicial em segundos: MTA (397,500 ±10,606); Nióbio 10% (294,333 + 90,897) e Nióbio 20% (279,000 + 15,874). O tempo de presa final para os grupos foram: MTA (15,000 + 49,497), Nióbio 10% (560 ±38,587), sendo menor quando comparado ao MTA (p<0,001) e Nióbio 20% (715,666 ± 30,664) (p<0,01). Os valores da radiopacidade em mm Al do Nióbio 10% (3,888 ±0,340); Nióbio 20% (3,713 ± 0,712). A resistência a compressão em MPa foi: Nióbio 10% (694,150 + 78,951) Nióbio 20% (699,295 + 47,672). A viabilidade celular não apresentou diferença entre o MTA e grupos experimentais (p<0,05). Os resultados da capacidade osteogênese das formulações a partir do ensaio da fosfatase alcalina (FAL) em UI/L por grama de proteína para cada grupo foi: MTA (1,9 + 1,227) e Nióbio 20% (1,784 + 1,342) (p>0,05). Nossos achados apontam propriedades relevantes para as formulações com Nb2O5 como, pH alcalino, radiopacidade, resistência a compressão e atividade da fosfatase alcalina (AU).

Work aimed to develop, characterize and evaluate the osteogenic activity of PC formulations with different proportions of Niobium oxide (Nb2O5), replacing Bi2O3. Three groups were used, one control and two experimental: GC (MTA Angelus®), F6 (75% CP, 20% Nb2O5 and 5% CaSO4) and F7 (75% CP, 10% Bi2O3, 10% Nb2O5e 5% CaSO4) . The formulations were submitted to X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), X-ray Fluorescence Spectrometry (FRX), pH, setting, radiopacity, compressive strength, cytotoxicity and bioactivity. The data obtained were statistically evaluated by the test of variance (ANOVA) with Bonferroni correction (p<0.05%). The pH test result: Niobium 10% Immediate (12.205 ±0.304); 24h; (12.770 ± 0.226) 48h: (12.910 ± 0.169). Niobium 20%: immediate (12.080 ± 0.282); 24h: (12.350 ± 0.593); 48 h: (12.580 ± 0.73). For initial setting time in seconds: MTA (397,500 ±10,606); Niobium 10% (294,333 + 90,897) and Niobium 20% (279,000 + 15,874). The final setting time for the groups were: MTA (15,000 + 49,497), Niobium 10% (560 ± 38,587), being smaller when compared to MTA (p<0,001) and Niobium 20% (715,666 ± 30,664) (p<0 .01). Radiopacity values in mm Al of 10% Niobium (3.888 ±0.340); Niobium 20% (3.713 ± 0.712). The compressive strength in MPa was: Niobium 10% (694.150 + 78.951) Niobium 20% (699.295 + 47.672). Cell viability showed no difference between MTA and experimental groups (p<0.05). The results of the osteogenesis capacity of the formulations from the alkaline phosphatase assay (ALF) in IU/L per gram of protein for each group were: MTA (1.9 + 1.227) and Niobium 20% (1.784 + 1.342) (p> 0.05). Our findings point to relevant properties for Nb2O5 formulations such as alkaline pH, radiopacity, compressive strength and alkaline phosphatase activity (AU).

Preparation and characterization of novel as-cast Ti-Mo-Nb alloys for biomedical applications.

Ti and its alloys are the most used metallic biomaterials devices due to their excellent combination of chemical and mechanical properties, biocompatibility, and non-toxicity to the human body. However, the current alloys available still have several issues, such as cytotoxicity of Al and V and high elastic modulus values, compared to human bone. ß-type alloys, compared to α-type and (α + ß)-type Ti alloys, have lower elastic modulus and higher mechanical strength. Then, new biomedical ß-type alloys are being developed with non-cytotoxic alloying elements, such as Mo and Nb. Therefore, Ti-5Mo-xNb system alloys were prepared by argon arc melting. Chemical composition was evaluated by EDS analysis, and the density measurements were performed by Archimedes' method. The structure and microstructure of the alloys were obtained by X-ray diffraction and optical and scanning electron microscopy. Microhardness values were analyzed, and MTT and crystal violet tests were performed to assess their cytotoxicity. As the Nb concentration increases, the presence of the ß-Ti phase also grows, with the Ti-5Mo-30Nb alloy presenting a single ß-Ti phase. In contrast, the microhardness of the alloys decreases with the addition of Nb, except the Ti-5Mo-10Nb alloy, which has its microhardness increased probably due to the ω phase precipitation. Biological in-vitro tests showed that the alloys are not cytotoxic.

3D printing of poly(butylene adipate-co-terephthalate) (PBAT)/niobium containing bioactive glasses (BAGNb) scaffolds: Characterization of composites, in vitro bioactivity, and in vivo bone repair.

This study aimed to produce poly(butylene adipate-co-terephthalate) (PBAT)/niobium containing bioactive glasses (BAGNb) composites scaffolds produced by fused deposition modeling (FDM) printing and evaluate their physicochemical and biological properties in vitro and in vivo. The composite filaments were produced by melt-extrusion with the addition of 10 wt% of BAGNb (PBAT/BAGNb). Filaments without BAGNb were produced as the control group (PBAT). The filaments were characterized and were used to produce 3D-printed scaffolds using FDM. The scaffolds' structure and surface properties were assessed. In vitro cell, proliferation, and cell mineralization analysis were performed. In vivo data was obtained in the rat femur model (n = 10), and the bone repair was assessed after 15, 30, and 60 postoperative days. The printed structures presented 69.81% porosity for the PBAT/BAGNb group and 74.54% for the PBAT group. Higher cell mineralization was observed for the PBAT/BAGNb group. The in vivo data showed that the PBAT/BAGNb presented new bone formation comparable to positive controls. The combination of PBAT and BAGNb in 3D-printed scaffolds may be an alternative to produce bioactive materials with controllable shapes and properties for bone regeneration treatments.

Low Mg content on Ti-Nb-Sn alloy when in contact with eBMMSCs promotes improvement of its biological functions.

Magnesium is a metal used in the composition of titanium alloys and imparts porosity. Due to its osteoconductive, biocompatible and biodegradable characteristics, its application in the development of biomedical materials has become attractive. This study aimed to evaluate the influence of magnesium present in porous Ti-Nb-Sn alloys, which have a low elastic modulus in adhesive, osteogenic properties and the amount of reactive intracellular oxygen species released in mesenchymal stem cells derived from bone marrow equine bone (eBMMSCs). Mechanical properties of the alloy, such as hardness, compressive strength and elastic modulus, were analyzed, as well as surface morphological characteristics through scanning electron microscopy. The evaluation of magnesium ion release was performed by atomic force spectroscopy. The biological characteristics of the alloy, when in contact with the alloy surface and with the culture medium conditioned with the alloy, were studied by SEM and optical microscopy. Confirmation of osteogenic differentiation by alizarin red and detection of ROS using a Muse® Oxidative Stress Kit based on dihydroetide (DHE). The alloy showed an elastic modulus close to cortical bone values. The hardness was close to commercial Ti grade 2, and the compressive strength was greater than the value of cortical bone. The eBMMSCs adhered to the surface of the alloy during the experimental time. Osteogenic differentiation was observed with the treatment of eBMMMSCs with conditioned medium. The eBMMSCs treated with conditioned medium decreased ROS production, indicating a possible antioxidant defense potential of magnesium release.

Potential of Nb2O5 nanofibers in photocatalytic degradation of organic pollutants.

Various photocatalytic nanomaterials for environmental remediation have been promoted due to the pollution caused by different organic pollutants. In this study, Nb2O5 nanofibers were obtained by electrospinning technique, presenting controlled crystallinity and high specific surface area to improve the photoactivity response. The structural characterization indicated Nb2O5 nanofibers with orthorhombic phase formation. The photoluminescence measurements showed different energy levels contributing to the electronic transition events. The nanofibers with a bandgap up to 3.6 eV were applied to photocatalysis of dyes (rhodamine B (RhB) or methylene blue (MB)) and fluoxetine (FLX), listed as an emergent pollutant. In the optimized condition (pH = 9), the RhB and MB photocatalysis was 59% and 93% more efficient than photolysis due to ζ = - 50 mV ± 5 for EtOH_550 sample increased interaction with MB (cationic) compared to RhB unprotonated (pKa = 3.7). Therefore, FLX (pKa = 10.7) was selected due to protonated form at pH = 9 and showed 68% ± 1 adsorption in 30 min for EtOH_550. The FLX photocatalytic degradation under UV light irradiation was up to 17% higher than the photolytic degradation. The formation of hydroxyl radicals in the photocatalytic system (EtOH_550) was proven by the Coumarine probe assay, corroborating with the greater amount of α-[2-(methylamino)ethyl]benzylalcohol (MAEB), a by-product obtained after FLX oxidation. Additionally, the material achieved specific catalytic activity for the different organic compounds (RhB, MB, or FLX). Therefore, Nb2O5 nanofibers were efficient for degrading three different pollutants under UV light, proving a viable alternative for environmental remediation.

New insights of Nb2O5-based coatings on the 316L SS surfaces: enhanced biological responses.

This communication aims to propose new insights of Nb2O5-based coatings on the 316L SS surface with great prospects to be used in the dentistry field as brackets. The Nb2O5 thin film was incorporated into the 316L SS by using PVD method. For this purpose, the studied system was characterized structurally and morphologically by using AFM, FTIR-IRRAS, Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). Biological assays were performed using human gingival fibroblast cell-line HGF-1. In agreement with FTIR and Raman results, the XPS technique indicates that Nb is present in an oxidation state assigned to Nb2O5. Furthermore, the coatings produced by PVD technique are less toxic and induces less inflammation in gingival cells (cell-line HGF-1), suggesting the strategy of use Nb2O5 thin film to cover the 316L SS promoted since its protection of the physiological environment to its biocompatibility improvement.

Fast pyrolysis as a tool for obtaining levoglucosan after pretreatment of biomass with niobium catalysts.

Levoglucosan (LGA) is a promising chemical platform derived from the pyrolysis of biomass that offers access to a variety of value-added products. We report an efficient route to produce LGA via the pretreatment of biomass with niobium compounds (oxalate, chloride and oxide) followed by fast pyrolysis coupled with gas chromatography-mass spectrometry (Py-GC-MS) at temperatures of 350-600 °C. Catalytic pretreatment reduces the quantity of lignin in the biomass, concentrates the cellulose and enhance LGA formation during fast pyrolysis. The pretreatment also removes alkaline metals, preventing competitive side reactions. The effect of several parameters such as catalyst weight, time, temperature, and solvent, with the optimal pretreatment conditions determined to be 3 (wt.%) niobium oxalate for 1 h at 23 °C in water. Pretreatment increased the LGA yields by 6.40-fold for sugarcane bagasse, 4.15-fold for elephant grass, 4.13-fold for rice husk, 2.86-fold for coffee husk, and 1.86-fold for coconut husk as compared to the raw biomasses. These results indicate that biomass pretreatment using niobium derivates prior fast pyrolysis can be a promising technique for biomass thermochemical conversion in LGA and others important pyrolytic products.

Nb-MCM-Type Mesoporous Material Synthesis Using Ionic Solid as Structure-Directing Agent for In Situ Lipase Immobilization.

MCM-41 and MCM-48 with niobium were successfully synthesized using 1-tetradecyl-3-methylimidazolium chloride ([C14MI]Cl) as a structure-directing agent. The best Si/Nb molar ratio was chosen (Si/Nb = 20) and the CALB enzyme was immobilized in situ in the synthesized Nb-MCM. SEM micrographs showed the formation of very regular spherical agglomerates with a diameter between 0.25 and 0.75 µm. The material presented a surface area of 954 and 704 m2/g and a pore volume of 0.321 and 0.286 cm3/g, for Nb-MCM-41 and Nb-MCM-48, respectively. Also, both materials showed a pore size of 2.261 nm. The number of recycles obtained for the CALB enzyme immobilized in Nb-MCM-41 and Nb-MCM-48 was 26 recycles with a residual activity of 49.62% and 16 recycles with a residual activity of 53.01%, respectively. For both materials, enzymatic activity remained stable for 5 months of storage at room temperature and refrigeration. The supports were able to catalyze the esterification reaction at 40, 60, and 80 °C, showing industrial application in reactions that require high temperatures. This methodology allows the preparation of new highly active and selective enzyme catalysts using niobium and [C14MI]Cl. Also, the new materials can provide greater viability in processes, ensuring a longer service life of catalysts. Graphical abstract.

Photocatalytic degradation of real textile wastewater using carbon black-Nb2O5 composite catalyst under UV/Vis irradiation.

This work investigated the impregnation of Nb2O5 into carbon black (CB) in different ratios and its effect in photocatalytic degradation of real wastewater from a dyeing factory by advanced oxidative processes (AOP). Synthesized catalysts were characterized regarding their crystalline structure (DRX, micro-Raman), morphology (MEV), textural (BET area) and optical properties (bandgap energy by diffuse reflectance) and pH at the point of zero charge (pHpzc). Preliminary tests showed better photodegradation results in the acidic medium after 5 h of irradiation with NCB-0.5 (Nb2O5:CB 0.5:1). Treatment parameters optimization was carried out using response surface methodology based on Box-Behnken experimental design. Catalyst concentration, solution pH and irradiation time were varied, analysing absorbance reduction (285 and 574 nm), COD and TOC removal after treatment as responses. The composite catalyst showed improved photocatalytic activity, attributed to an increase in adsorption capacity and the bandgap narrowing, redshifting the absorption edge wavelength to the visible region, brought by CB impregnation. Optimal conditions were found at 0.250 g L-1 of catalyst, pH 2.0 and 5 h of irradiation, removing 72.19% and 93.52% of absorbance in 285 and 574 nm, respectively, 51.29% of COD and 70.70% of TOC using NCB-0.5.

Visible-light Bi-Fe-Nb-O photoanodes for solar-light driven hydrogen production.

Currently, CO2 emission is the main cause of climate change and its various related environmental impacts. Therefore, we have as a prime the development of clean sources of energy. The hydrogen economy is very attractive in this regard, however, when generated from the methane reform, there are also large-scale CO2 emissions. Thus, this research aims to develop and characterize bismuth and iron niobate-based photoanodes for hydrogen production via water photoelectrolysis. Bi2FexNbO7 films were synthesized by the sol-gel method and deposited on FTO coated glass plates by dip-coating technique. The influence of heat treatment (400, 500 and 600°C) and amount of iron on the structure (Bi2FexNbO7, x = 0, 0.8, 1, 1.2) were evaluated. Optical, structural and morphological properties were performed, as well as photoanode efficiency in photocurrent assays. The results indicate that the increase of temperature as well as the amount of iron leads to a higher absorption capacity and hence to lower band gap values. Regarding the structural properties, it was possible to observe the BFNO phase in the samples treated at 500 and 600°C. The films heat-treated at 400°C had a heterogeneous texture and a good covering. At 600°C there were some cracks in films surface. Therefore, samples with more iron and treated at 400°C showed better responses in photocurrent assays. It can be concluded that bismuth-iron niobate has a great potential to be applied in photoelectrolysis hydrogen production.