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1.
Sci Rep ; 13(1): 21238, 2023 Dec 01.
Article in English | MEDLINE | ID: mdl-38040735

ABSTRACT

This study focuses on the synthesis and characterization of supercapacitor materials derived from pyrolyzed natural compounds. Four compounds were investigated: methylcellulose with lysine (ML), methylcellulose with lysine-graphene composite (MLG), algae (A), and algae-graphene composite (AG). The pyrolysis process was utilized to convert these natural compounds into carbon-based materials suitable for supercapacitor applications. The properties of the resulting materials were analyzed extensively to evaluate their potential as supercapacitor electrodes. The electrochemical performance, including specific capacitance, cyclic stability, and rate capability was measured using various characterization techniques. The effects of incorporating graphene into the lysine-methylcellulose and algae matrices were also studied to explore the enhancements in supercapacitor performance. In both cases, the addition of graphene resulted in a positive effect. Among all the materials investigated, the algae-graphene composite exhibited the most favorable properties, demonstrating a specific capacitance of 192 F g-1 after 10,000 galvanostatic charge-discharge cycles at a current of 5 A g-1 in K2SO4 electrolyte. This exceptional performance underscores the potential of the algae-graphene composite as a highly efficient and durable electrode material for supercapacitor applications.

2.
Sci Rep ; 13(1): 18632, 2023 Oct 30.
Article in English | MEDLINE | ID: mdl-37903853

ABSTRACT

Hybrid materials featuring perovskite-type metal oxide in conjunction with heteroatom-doped graphene hold immense promise as alternatives to costly noble metal catalysts for electrochemical water splitting, facilitating the generation of environmentally friendly hydrogen. In this study, perovskite-type oxide containing praseodymium, barium, strontium, cobalt, and iron atoms dispersed in a carbon matrix as a catalyst is synthesized via annealing of the carbon material with substrates for the preparation of perovskite oxide. The mass ratio of reagents regulates the porous structure and elemental composition. The result of the hydrogen evolution reaction (HER), suggests that the hybrid catalysts exhibit intermediate HER kinetics compared to the commercial Pt/C and the catalyst without carbon. The Tafel slope for HER is lower for materials containing carbon, because of the improved reaction kinetics, facilitated proton transfer, and enhanced electrochemical surface area. Therefore, the study provides an effective strategy for the preparation of catalyst and their use as the active catalyst of water splitting.

3.
RSC Adv ; 13(36): 25437-25442, 2023 Aug 21.
Article in English | MEDLINE | ID: mdl-37636512

ABSTRACT

Gelatine and chitosan were used as natural precursors for nitrogen-doping of the graphene foam structure, creating specific types of active sites. The quantitative and qualitative content of nitrogen groups in the carbon structure was determined, which, under the influence of high temperature, were incorporated and transformed into forms of functional groups favorable for electrochemical application. Electrochemical studies proved that the form of pyridine-N, pyrrole-N, and quaternary-N groups have favorable electrochemical properties in the oxygen reduction reaction comparable to commercial platinum-based electrode materials. Using these materials as electrodes in metal-air batteries or fuel cells may eliminate the use of noble metal-based electrodes.

4.
RSC Adv ; 13(15): 10215-10220, 2023 Mar 27.
Article in English | MEDLINE | ID: mdl-37006354

ABSTRACT

The aim of the conducted research was to develop hybrid nanostructures formed from MnCo2O4 and exfoliated graphite. Carbon added during the synthesis allowed for obtaining a well-distributed MnCo2O4 particle size with exposed active sites contributing to the increased electric conductivity. The influence of the weight ratios of carbon to a catalyst for hydrogen and oxygen evolution reactions was investigated. The new bifunctional catalysts for water splitting were tested in an alkaline medium with excellent electrochemical performance and very good working stability. The results for hybrid samples show better electrochemical performance compared to the pure MnCo2O4. The highest electrocatalytic activity was for sample MnCo2O4/EG (2/1), where the value of the overpotential was 1.66 V at 10 mA cm-2, and also for this sample a low value of Tafel slope (63 mV dec-1) was denoted.

5.
Sci Rep ; 12(1): 22577, 2022 Dec 30.
Article in English | MEDLINE | ID: mdl-36585427

ABSTRACT

Herein, we demonstrate that modification of TiO2 nanotubes with graphene-strontium and cobalt molybdate perovskite can turn them into active electrocatalysts for hydrogen evolution reaction (HER). For this purpose, a simple method of hydrothermal synthesis of perovskites was developed directly on the TiO2 nanotubes substrate. Moreover, the obtained hybrids were also decorated with graphene oxide (GO) during one-step hydrothermal synthesis. The obtained materials were characterized by scanning electron microscopy with energy dispersive X-ray analysis, Raman spectroscopy, and X-ray diffraction analysis. Catalytic properties were verified by electrochemical methods (linear voltammetry, chronopotentiometry). The obtained hybrids were characterized by much better catalytic properties towards hydrogen evolution reaction compared to TiO2 and slightly worse than platinum. The optimized hybrid catalyst (decorated by GO) can drive a cathodic current density of 10 mA cm-2 at an overpotential of 121 mV for HER with a small Tafel slope of 90 mV dec-1 in 0.2 M H2SO4.

6.
J Clin Med ; 11(20)2022 Oct 19.
Article in English | MEDLINE | ID: mdl-36294479

ABSTRACT

The reason why marginal bone loss (MBL) occurs after dental implant insertion without loading has not yet been clearly investigated. There are publications that confirm or reject the notion that there are factors that induce marginal bone loss, but no research investigates what exactly occurs in the bone surrounding the implant neck. In this study, 2196 samples of dental implant neck bone radiographs were analyzed. The follow-up period was 3 months without functional loading of the implant. Marginal bone loss was evaluated in relation to the torque used during the final phase of implant insertion. Radiographic texture features were also analyzed and evaluated. The analyses were performed individually for the anterior and posterior part of the alveolar crest in both the mandible and maxilla. After 3 months, an MBL relation with higher torque (higher than 40 Ncm; p < 0.05) was observed, but only in the lower jaw. The texture features Sum Average (SumAverg), Entropy, Difference Entropy (DifEntr), Long-Run Emphasis (LngREmph), Short-Run Emphasis (ShrtREmph), and discrete wavelet decomposition transform features were changed over time. This study presents that MBL is related to the torque value during dental implant insertion and the location of the procedure. The increasing values of SumAverg and LngREmph correlated with MBL, which were 64.21 to 64.35 and 1.71 to 2.01, respectively. The decreasing values of Entr, DifEntr, and ShrtREmph also correlated with MBL, which were 2.58 to 2.47, 1.11 to 1.01, and 0.88 to 0.84, respectively. The analyzed texture features may become good indicators of MBL in digital dental surgery.

7.
Nanomaterials (Basel) ; 12(18)2022 Sep 12.
Article in English | MEDLINE | ID: mdl-36144944

ABSTRACT

In this paper, we present the results of the gamma irradiation method to obtain N-doped mesoporous activated carbons. Nitrogen-enriched mesoporous carbons were prepared from three chosen commercial activated carbons such as Carbon Black OMCARB C-140, KETJENBLACK EC-600JD and PK 1-3 Norit. HRTEM, SEM, Raman spectra, elemental analysis, XPS studies and widely approved N2 adsorption-desorption measurements allowed us to evaluate the effectiveness of N atom insertion and its influence on the BET surface area and the pore structure of modified carbons. The obtained materials have an exceptionally high N content of up to 3.2 wt.%. Additionally, selected N-doped activated carbons were fully characterized to evaluate their applicability as carbon electrode materials with particular emphasis on Oxygen Reduction Reaction (ORR). The proposed method is a relatively facile, efficient and universal option that can be added to the already known methods of introducing heteroatoms to different carbons.

8.
J Clin Med ; 11(12)2022 Jun 20.
Article in English | MEDLINE | ID: mdl-35743625

ABSTRACT

The phenomenon of peri-implant bone corticalization after functional loading does not yet have a definite clinical significance and impact on prognosis. An attempt was made to assess the clinical significance of this phenomenon. This prospective study included 554 patients. Standardized intraoral radiographs documenting the jawbone environment of 1556 implants were collected. The follow-up period was 10 years of functional loading. Marginal alveolar bone loss (MBL) and radiographic bone structure (bone index, BI) were evaluated in relation to intraosseous implant design features and prosthetic work performed. After five years, bone structure abnormalities expressed by a reduction of BI to 0.47 ± 0.21 and MBL = 0.88 ± 1.27 mm were observed. Both values had an inverse relationship with each other (p < 0.0001). Reference cancellous bone showed BI = 0.85 ± 0.18. The same relationship was observed after ten years of functional loading: BI = 0.48 ± 0.21, MBL = 1.49 ± 1.94 mm, and again an inverse relationship (p < 0.0001). Increasing corticalization (lower BI) is strongly associated with increasing marginal bone loss and increasing corticalization precedes future marginal bone loss. Marginal bone loss will increase as corticalization progresses.

9.
Sci Rep ; 11(1): 23970, 2021 Dec 14.
Article in English | MEDLINE | ID: mdl-34907258

ABSTRACT

The production of effective catalysts in the oxygen reduction reaction (ORR) continues to be a great challenge for scientists. A constant increase in demand for energy storage materials is followed by a proportionate increase in the number of reports on electrocatalyst synthesis. The scientific world focuses on environmentally friendly materials synthesized in accordance with the safest possible. In this work, we developed a facile method of obtaining heavy-metal-free electrode materials that are effective in ORR. Graphene-based catalysts were doped using azodicarbonamide (ADC) as the source of nitrogen, then carbonized at high temperatures in the range of 700-900 °C under inert gas flow. The produced materials were tested as catalysts for ORR, which is the most important reaction for Zn-air batteries and fuel cells. All obtained nitrogen-doped graphene foams showed increased catalytic activity in ORR owing to active sites created by nitrogen functional groups on the graphene surface. This paper shows that carbonization temperature has a significant impact on nitrogen content and that a small percentage of nitrogen may have a positive effect on the catalytic activity of the obtained materials. The number of transferred electrons in ORR was found to range from three to the maximal theoretical value, i.e., four.

10.
Sci Rep ; 11(1): 22054, 2021 Nov 11.
Article in English | MEDLINE | ID: mdl-34764324

ABSTRACT

The manuscript presents results on the influence of external pressure on graphene exfoliation and subsequent 3D structuring by means of liquid-phase exfoliation. In contrast to known and applied exfoliation methods, the current study exploits the enhancement of splitting forces caused by the application of high pressure. The manufacturing pathway allowed to increase the surface area from 750 m2/g (nanoplatelets) to ca. 1100 m2/g (after 3D structuring). Electrochemical studies revealed that the 3D graphene materials were active in the oxygen reduction reaction (ORR). The outstanding ORR activity of 3D structured graphene materials should not be ascribed to heteroatom catalytic centers since such heteroatoms were successively removed upon increasing the carbonization temperature. XPS data showed that the presence of transition metals and nitrogen (usually regarded as catalytic centers) in G-materials was marginal. The results highlight the importance of structural factors of electrodes in the case of graphene-based materials for Zn-air batteries and ORR.

11.
Sci Rep ; 11(1): 18387, 2021 09 15.
Article in English | MEDLINE | ID: mdl-34526635

ABSTRACT

In this work, nitrogen-doped porous carbons obtained from chitosan, gelatine, and green algae were investigated in their role as supercapacitor electrodes. The effects of three factors on electrochemical performance have been studied-of the specific surface area, functional groups, and a porous structure. Varying nitrogen contents (from 5.46 to 10.08 wt.%) and specific surface areas (from 532 to 1095 m2 g-1) were obtained by modifying the carbon precursor and the carbonization temperature. Doping nitrogen into carbon at a level of 5.74-7.09 wt.% appears to be the optimum for obtaining high electrochemical capacitance. The obtained carbons exhibited high capacitance (231 F g-1 at 0.1 A g-1) and cycle durability in a 0.2 mol L-1 K2SO4 electrolyte. Capacitance retention was equal to 91% at 5 A g-1 after 10,000 chronopotentiometry cycles. An analysis of electrochemical behaviour reveals the influence that nitrogen functional groups have on pseudocapacitance. While quaternary-N and pyrrolic-N nitrogen groups have an enhancing effect, due to the presence of a positive charge and thus improved electron transfer at high current loads, the most important functional group affecting energy storage performance is graphite-N/quaternary-N. The study points out that the search for the most favourable organic precursors is as important as the process of converting precursors to carbon-based electrode materials.

12.
Nanomaterials (Basel) ; 11(3)2021 Mar 17.
Article in English | MEDLINE | ID: mdl-33803051

ABSTRACT

This paper addresses the problem of improving electrochemical energy storage with electrode materials obtained from common raw ingredients in a facile synthesis. In this study, we present a simple, one-pot route of synthesizing microporous carbon via a very fast reaction of sucrose and graphene (carbon source), chitosan (carbon and nitrogen source), and H3PO4. Porous carbons were successfully produced during high temperature carbonization, using nitrogen as a shielding gas. Samples were characterized using X-ray powder diffractometry, elemental analysis, N2 adsorption-desorption measurements, scanning electron microscopy, and Raman spectroscopy. The developed carbon material possessed a high surface area, up to 1313 m2 g-1, with no chemical or physical activators used in the process. The structural parameters of the microporous carbons varied depending on the ratio of reagents and mass composition. Samples were prepared both with and without chitosan. The present synthesis route has the advantages of being a single-step approach and only involving low-cost and environmentally friendly sources of carbon. More importantly, microporous carbon was prepared without any activators and potentially offers great application in supercapacitors. Cyclic voltammetry and constant current charge-discharge tests show that sucrose-based porous carbons show excellent electrochemical performance with a specific capacitance of up to 143 F g-1 at a current density of 1 A g-1 in a 6 M KOH electrolyte.

13.
Sci Rep ; 11(1): 7084, 2021 Mar 29.
Article in English | MEDLINE | ID: mdl-33782447

ABSTRACT

The development of effective catalysts for the oxygen reduction reaction (ORR) is a significant challenge in energy conversion systems, e.g., Zn-air batteries. Herein, green-algae- and gelatine-derived porous, nitrogen-rich carbons were extensively investigated as electrode materials for electrochemical catalytic reactions. These carbon-based catalysts were designed and optimized to create a metal-free catalyst via templating, carbonization, and subsequent removal of the template. The additional incorporation of graphene improved electronic conductivity and enhanced the electrochemical catalytic reaction. Porous carbons with heteroatoms were used as effective platinum-free ORR electrocatalysts for energy conversion; the presence of nitrogen in the carbon provided more active sites for ORR. Our catalyst also displayed notable durability in a rechargeable Zn-air battery energy system. More importantly, the nitrogen-containing porous carbons were found to have comparable ORR performance in alkaline media to commercially available electrocatalysts. The manuscript demonstrates that nitrogen atom insertion is an appropriate approach when aiming to eliminate noble metals from the synthesis route. N-doped carbons are competitive materials compared to reference platinum-based catalysts.

14.
Sci Rep ; 11(1): 2044, 2021 Jan 21.
Article in English | MEDLINE | ID: mdl-33479478

ABSTRACT

The synthesis of metal-free but electrochemically active electrode materials, which could be an important contributor to environmental protection, is the key motivation for this research approach. The progress of graphene material science in recent decades has contributed to the further development of nanotechnology and material engineering. Due to the unique properties of graphene materials, they have found many practical applications: among others, as catalysts in metal-air batteries, supercapacitors, or fuel cells. In order to create an economical and efficient material for energy production and storage applications, researchers focused on the introduction of additional heteroatoms to the graphene structure. As solutions for functionalizing pristine graphene structures are very difficult to implement, this article presents a facile method of preparing nitrogen-doped graphene foam in a microwave reactor. The influence of solvent type and microwave reactor holding time was investigated. To characterize the elemental content and structural properties of the obtained N-doped graphene materials, methods such as elemental analysis, high-resolution transmission electron microscopy, scanning electron microscopy, and Raman spectroscopy were used. Electrochemical activity in ORR of the obtained materials was tested using cyclic voltamperometry (CV) and linear sweep voltamperometry (LSV). The tests proved the materials' high activity towards ORR, with the number of electrons reaching 3.46 for tested non-Pt materials, while the analogous value for the C-Pt (20 wt% loading) reference was 4.

15.
Materials (Basel) ; 13(13)2020 Jul 06.
Article in English | MEDLINE | ID: mdl-32640535

ABSTRACT

The N-doped hybrid carbon materials containing amorphous carbon nanotubes (ACNTs) were obtained by free growth of a polymer at 200 °C. The improvement of electrical conductivity was achieved by a final carbonization at 600-800 °C under the flow of nitrogen. The microstructure of ACNT/N-doped hybrids was characterized using a transmission electron microscope and X-ray diffusion. Furthermore, their elemental composition was measured using energy-dispersive X-ray spectroscopy and an elemental analyzer. The experimental results indicated that the ACNTs had a diameter in the range of 40-60 nm and the N-doped carbon background contained nitrogen atoms in most bonded pyrrolic-N and quaternary-N groups. The results revealed that the microstructure of the as-grown nanotubes, prepared by the proposed method, is mainly amorphous. This technique introduces the advantages of low cost and process simplicity, which may redeem some drawbacks of the methods commonly used in ACNT synthesis.

16.
Materials (Basel) ; 13(9)2020 May 02.
Article in English | MEDLINE | ID: mdl-32370239

ABSTRACT

The constantly growing demand for active, durable, and low-cost electrocatalysts usable in energy storage devices, such as supercapacitors or electrodes in metal-air batteries, has triggered the rapid development of heteroatom-doped carbon materials, which would, among other things, exhibit high catalytic activity in the oxygen reduction reaction (ORR). In this article, a method of synthesizing nitrogen-doped graphene is proposed. Few-layered graphene sheets (FL-graphene) were prepared by electrochemical exfoliation of commercial graphite in a Na2SO4 electrolyte with added calcium carbonate as a separator of newly-exfoliated FL-graphene sheets. Exfoliated FL-graphene was impregnated with a suspension of green algae used as a nitrogen carrier. Impregnated FL-graphene was carbonized at a high temperature under the flow of nitrogen. The N-doped FL-graphene was characterized through instrumental methods: high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, and Raman spectroscopy. Electrochemical performance was determined using cyclic voltamperometry and linear sweep voltamperometry to check catalytic activity in ORR. The N-doped electroexfoliated FL-graphene obeyed the four-electron transfer pathways, leading us to further test these materials as electrode components in rechargeable zinc-air batteries. The obtained results for Zn-air batteries are very important for future development of industry, because the proposed graphene electrode materials do not contain any heavy and noble metals in their composition.

17.
J Med Chem ; 62(23): 10711-10739, 2019 12 12.
Article in English | MEDLINE | ID: mdl-31710483

ABSTRACT

Histone deacetylase 6 (HDAC6) is a peculiar HDAC isoform whose expression and functional alterations have been correlated with a variety of pathologies such as autoimmune disorders, neurodegenerative diseases, and cancer. It is primarily a cytoplasmic protein, and its deacetylase activity is focused mainly on nonhistone substrates such as tubulin, heat shock protein (HSP)90, Foxp3, and cortactin, to name a few. Selective inhibition of HDAC6 does not show cytotoxic effects in healthy cells, normally associated with the inhibition of Class I HDAC isoforms. Here, we describe the design and synthesis of a new class of potent and selective HDAC6 inhibitors that bear a pentaheterocyclic central core. These compounds show a remarkably low toxicity both in vitro and in vivo and are able to increase the function of regulatory T cells (Tregs) at well-tolerated concentrations, suggesting a potential clinical use for the treatment of degenerative, autoimmune diseases and for organ transplantation.


Subject(s)
Histone Deacetylase 6/antagonists & inhibitors , Hydroxamic Acids/chemistry , Animals , Cell Survival/drug effects , Drug Design , Gene Expression Regulation, Enzymologic/drug effects , Histone Deacetylase 6/genetics , Histone Deacetylase 6/metabolism , Histones/metabolism , Mice , Protein Isoforms , Spleen/cytology , T-Lymphocytes, Regulatory , Tubulin/genetics , Tubulin/metabolism
18.
Nanomaterials (Basel) ; 9(7)2019 Jul 03.
Article in English | MEDLINE | ID: mdl-31277243

ABSTRACT

We demonstrate an accessible and effective technique for exfoliating graphite foil and graphite powder into graphene in a water solution of inorganic salt. In our research, we report an electrochemical cathodic exfoliation in an aqueous solution of Na2SO4. After electro-exfoliation, the resulting graphene was premixed with furfuryl alcohol (FA) and an inorganic template (CaCO3 and Na2CO3). Once FA was polymerized to poly(furfuryl alcohol) (PFA), the mixture was carbonized. Carbon bridges originating in thermally-decomposed PFA joined exfoliated graphene flakes and stabilized the whole sponge-type structure after the nano-template was removed. Gases evolved at the graphite electrode (cathode) played an important role in the process of graphene-flake splitting and accelerated the change of graphite into graphene flakes. Starting graphite materials and graphene sponges were characterized using Raman spectroscopy, SEM, high-resolution transmission electron microscopy (HRTEM), elemental analysis, and low-temperature adsorption of nitrogen to determine their structure, morphology, and chemical composition. The discovered manufacturing protocol had a positive influence on the specific surface area and porosity of the sponges. The SEM and HRTEM studies confirmed a high separation degree of graphite and different agglomeration pathways. Raman spectra were analyzed with particular focus on the intensities of ID and IG peaks; the graphene-type nature of the sponges was confirmed.

19.
Int J Biol Macromol ; 80: 605-9, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26193681

ABSTRACT

Collagen was extracted from the skin of Brama australis, the fish from warm-water sea. The yield of collagen from skin of B. australis was about 1.5% on a wet weight basis of raw material. The isolated protein was confirmed as collagen by different physico-chemical techniques such as: FTIR, SDS-PAGE, and amino acid analysis. The denaturation temperature (T(d)) of obtained collagen was found to be 24°C, what is promising as an advantage for cosmetic application. According to the electrophoretic pattern, collagen consisted of two different α-chains (α1 and α2) and was classified as type I collagen. Although T(d) of obtained collagen is higher than 20 °C it is still far from T(d) of mammalian collagen.


Subject(s)
Collagen/chemistry , Collagen/isolation & purification , Fishes , Skin/chemistry , Amino Acids/chemistry , Animals , Collagen Type I/chemistry , Collagen Type I/isolation & purification , Electrophoresis, Polyacrylamide Gel , Protein Denaturation , Spectroscopy, Fourier Transform Infrared , Temperature
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