Analysis of the Surface Condition and Changes in Crystallographic Structure of Zirconium Oxide Affected by Mechanical Processing

Zirconium oxide is a material commonly used in dental prosthetics for making cups of permanent prosthetic restorations. In order to properly prepare the surface of zirconium oxide for prosthetic treatment, it must be veneered with ceramics. The quality of cup-veneered ceramics is dependent on many factors, including the surface free energy (SFE) and transformation of zirconium oxide. The aim of the study was to investigate the type of phase transition and the value of free energy of the surface subjected to machining (wet and dry grinding, polishing). Quantitative and qualitative phase identification measurements showed that mechanical treatment causes transformation of the tetragonal phase into a monoclinic phase in the zirconium oxide surface. Prepared samples were analyzed by means of X-ray diffraction (XRD), which confirmed the phenomenon of transition. Measurements of the wetting angle and the calculated values of the surface free energy (SFE) showed no significant differences between the samples subjected to each treatment     

Gas-Phase Deposition of Ultrathin Aluminium Oxide Films on Nanoparticles at Ambient Conditions

We have deposited aluminium oxide films by atomic layer deposition on titanium oxide nanoparticles in a fluidized bed reactor at 27 ± 3 °C and atmospheric pressure. Working at room temperature allows the coating of heat-sensitive materials, while working at atmospheric pressure would simplify the scale-up of this process. We performed 4, 7 and 15 cycles by dosing a predefined amount of precursors, i.e., trimethyl aluminium and water. We obtained a growth per cycle of 0.14–0.15 nm determined by transmission electron microscopy (TEM), similar to atomic layer deposition (ALD) experiments at a few millibars and ~180 °C. We also increased the amount of precursors dosed by a factor of 2, 4 and 6 compared to the base case, maintaining the same purging time. The growth per cycle (GPC) increased, although not linearly, with the dosing time. In addition, we performed an experiment at 170 °C and 1 bar using the dosing times increased by factor 6, and obtained a growth per cycle of 0.16 nm. These results were verified with elemental analysis, which showed a good agreement with the results from TEM pictures. Thermal gravimetric analysis (TGA) showed a negligible amount of unreacted molecules inside the alumina films. Overall, the dosage of the precursors is crucial to control precisely the growth of the alumina films at atmospheric pressure and room temperature. Dosing excess precursor induces a chemical vapour deposition type of growth due to the physisorption of molecules on the particles, but this can be avoided by working at high temperatures.     

Influence of Abrasive Treatment on a Transformation of Zirconium Oxide Used in Dental Prosthetics

Zirconium oxide is a ceramic most often used in the field of dentistry for permanently cementing the substructures of prosthetic restorations in patients. The surface of zirconium oxide should be prepared properly because in the next stage it must be covered with porcelain. The success of prosthetics treatment depends on various factors, but it has been reported that the transformation of zirconium oxide plays a key role. The purpose of the research was to investigate the effect of abrasive blasting on the transformation of zirconium oxide. The research has shown that this type of surface treatment causes the transformation of the tetragonal phase into a monoclinic one. The samples were examined using X-ray diffraction (XRD). The study confirmed the assumption.     

Role of Nitric Oxide in the Regulation of Substrate Metabolism in Heart Failure

Solid experimental evidence indicates that nitric oxide (NO) inhibits oxygen utilization in vitro and in vivo. The role played by NO in cellular metabolism is likely extended to the control of substrate utilization. Studies performed in normal hearts show that NO inhibits glucose uptake and that a reduced synthesis of NO impairs free fatty acid consumption. Interestingly, we found also that myocardial free fatty acid utilization decreases while glucose consumption is enhanced in end stage heart failure, when cardiac NO production falls dramatically. This phenomenon led us to the hypothesis that the reduced synthesis of NO could be at least in part responsible for myocardial metabolic alterations occurring in severe heart failure. The present review mentions some of the seminal studies that defined the function of NO as metabolic modulator. A particular emphasis is put on available data suggesting a role for NO in the control of cardiac substrate utilization in normal and failing hearts.     

A Study of the Localized Ceria Coating Deposition on Fe-Rich Intermetallics in an AlSiFe Cast Alloy

Corrosion inhibiting conversion coating formation is triggered by the activity of micro-galvanic couples in the microstructure and subsequent local increase in pH at cathodic sites, which in the case of aluminium alloys are usually intermetallics. Ceria coatings are formed spontaneously upon immersion of aluminium alloys in a cerium conversion coating solution, the high pH gradient in the vicinity of intermetallics drives the local precipitation of ceria conversion compounds. Cu-rich intermetallics demonstrate a highly cathodic nature and have shown the local precipitation reaction to occur readily. Fe-rich intermetallics are, however, weaker cathodes and have shown varied extents of localized deposits and are in focus in the current work. Model cast Al-7wt.%Si alloys have been designed with 1 wt.% Fe, solidified at different cooling rates to achieve two different microstructures, with big and small intermetallics, respectively. Upon subjecting the two microstructures to the same conversion coating treatment (immersion in a 0.1 M CeCl₃ solution) for a short period of 2 h, preferential heavy deposition on the boundaries of the big intermetallics and light deposition on the small intermetallics was observed. Based on these observations, a mechanism of localized coating initiation at these Fe-rich intermetallic particles (IM) is proposed.     

Changes in the Structure and Corrosion Protection Ability of Porous Anodic Oxide Films on Pure Al and Al Alloys by Pore Sealing Treatment

It is well known that corrosion protection of pure Al is enormously improved by the formation of porous anodic oxide films and by pore sealing treatment. However, the effects of anodizing and pore sealing on corrosion protection for Al alloys are unclear, because the alloying elements included in Al alloys affect the structure of anodic oxide films. In the present study, porous anodic oxide films are formed on pure Al, 1050-, 3003- and 5052-Al alloys, and pore sealing was carried out in boiling water. Changes in the structure and corrosion protection ability of porous anodic oxide films on pure Al and the Al alloys by pore sealing, were examined by scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). SEM observation showed that anodic oxide films formed on pure Al have a smooth surface after pore sealing, and that cracks are formed in anodic oxide films on 1050-, 3003- and 5052-aluminum alloys, after pore sealing. Corrosion protection after pore sealing increased with anodizing time on pure Al, but only slightly increased with anodizing time on the Al alloys.     

The Role of Nitric Oxide in the Failing Heart

Nitric oxide (NO) has effects on contractility, energetics and gene expression of failing myocardium. Initial studies on isolated cardiomyocytes showed NO to reduce systolic shortening but intracoronary infusions of NO-donors or of NO synthase (NOS) inhibitors failed to elicit changes in baseline LV contractility indices such as LVdP/dt(max). Intracoronary infusions of NO-donors or of substance P, which releases NO from the coronary endothelium, however demonstrated NO to induce a downward displacement of the left ventricular (LV) diastolic pressure-volume relation, consistent with increased LV diastolic distensibility. In end-stage failing myocardium, the increased oxygen consumption is related to reduced NO production and in isolated cardiomyocytes, NO blunts the norepinephrine-induced expression of the fetal gene programme thereby preserving myocardial calcium homeostasis.In dilated cardiomyopathy, changed endomyocardial NOS gene expression has been reported. Because of lower endomyocardial NOS gene expression in patients with higher functional class and lower LV stroke work, increased endomyocardial NOS gene expression seems to be beneficial rather than detrimental for the failing heart. A beneficial effect of increased NOS gene expression could result from NO's ability to increase LV diastolic distensibility, to augment LV preload reserve, to reduce myocardial oxygen consumption and to prevent downregulation of calcium ATPase. Upregulated endomyocardial NOS gene expression has also been reported in athlete's heart and could therefore play a role in physiological LV remodeling. Reduced endomyocardial NO content because of decreased NO or increased superoxide production could lower LV diastolic distensibility and contribute to diastolic heart failure. In many conditions such as aging, hypertension, diabetes or posttransplantation, the increased incidence of diastolic heart failure is indeed paralleled by reduced endothelium-dependent vasodilation.     

Study of the Influence of Zirconium,Titanium and Strontium on the Properties and Microstructure of AlSi7Mg0.3Cu0.5 Alloy

The aim of the paper is to describe and specify the properties and microstructure of Al-Si alloy using Zr, a combination of Zr with elements used in the grafting of Al (Ti) alloys, and modification (Sr). Al-Si alloys with a combination of Zr and Ti and Sr elements represent an opportunity for the development of new aluminum alloys with a specific use. The experiment focused on the analysis of the synergistic effects of Zr with Ti and Zr with Sr on a AlSi7Mg0.3Cu0.5 alloy. The experimental alloys contained a constant Zr content of 0.15 wt. % and were alloyed with a gradual addition of Ti and Sr in the range of 0.1 to 0.3 wt. % for Ti, and 0.1 to 0.3 wt. % for Sr. The experimental samples were cast by meltable model casting technology. In variants with a constant addition of Zr 0.15 wt. % and a gradual addition of Ti, we observed an increase in the values of mechanical characteristics, with a significant decrease in ductility. When evaluating the structure of experimental alloys, Ti affected it by increasing the number of precipitated Zr phases. Experimental alloys with Zr and Sr addition were characterized by nucleation of Zr phases in angular morphology. It can be concluded that the investigated elements are expected to have a positive (strengthening) effect even at higher operating temperatures.     

Manganese–Cobalt Based Spinel Coatings Processed by Electrophoretic Deposition Method: The Influence of Sintering on Degradation Issues of Solid Oxide Cell Oxygen Electrodes at 750 °C

This paper seeks to examine how the Mn–Co spinel interconnect coating microstructure can influence Cr contamination in an oxygen electrode of intermediate temperature solid oxide cells, at an operating temperature of 750 °C. A Mn–Co spinel coating is processed on Crofer 22 APU substrates by electrophoretic deposition, and subsequently sintered, following both the one-step and two-step sintering, in order to obtain significantly different densification levels. The electrochemical characterization is performed on anode-supported cells with an LSCF cathode. The cells were aged prior to the electrochemical characterization in contact with the spinel-coated Crofer 22 APU at 750 °C for 250 h. Current–voltage and impedance spectra of the cells were measured after the exposure with the interconnect. Post-mortem analysis of the interconnect and the cell was carried out, in order to assess the Cr retention capability of coatings with different microstructures.     

The Effect of Electrophoretic Deposition Parameters on the Microstructure and Adhesion of Zein Coatings to Titanium Substrates

Zein coatings were obtained by electrophoretic deposition (EPD) on commercially pure titanium substrates in an as-received state and after various chemical treatments. The properties of the zein solution, zeta potential and conductivity, at varying pH values were investigated. It was found that the zein content and the ratio of water to ethanol of the solution used for EPD, as well as the process voltage value and time, significantly influence the morphology of coatings. The deposits obtained from the solution containing 150 g/L and 200 g/L of zein and 10 vol % of water and 90 vol % of ethanol, about 4–5 μm thick, were dense and homogeneous. The effect of chemical treatment of the Ti substrate surface prior to EPD on coating adhesion to the substrate was determined. The coatings showed the highest adhesion to the as-received and anodized substrates due to the presence of a thick TiO₂ layer on their surfaces and the presence of specific surface features. Coated titanium substrates showed slightly lower electrochemical corrosion resistance than the uncoated one in Ringer’s solution. The coatings showed a well-developed surface topography compared to the as-received substrate, and they demonstrated hydrophilic nature. The present results provide new insights for the further development of zein-based composite coatings for biomedical engineering applications.     

Unusual Dependence of the Diamond Growth Rate on the Methane Concentration in the Hot Filament Chemical Vapor Deposition Process

Although the growth rate of diamond increased with increasing methane concentration at the filament temperature of 2100 °C during a hot filament chemical vapor deposition (HFCVD), it decreased with increasing methane concentration from 1% CH₄ –99% H₂ to 3% CH₄ –97% H₂ at 1900 °C. We investigated this unusual dependence of the growth rate on the methane concentration, which might give insight into the growth mechanism of a diamond. One possibility would be that the high methane concentration increases the non-diamond phase, which is then etched faster by atomic hydrogen, resulting in a decrease in the growth rate with increasing methane concentration. At 3% CH₄ –97% H₂, the graphite was coated on the hot filament both at 1900 °C and 2100 °C. The graphite coating on the filament decreased the number of electrons emitted from the hot filament. The electron emission at 3% CH₄ –97% H₂ was 13 times less than that at 1% CH₄ –99% H₂ at the filament temperature of 1900 °C. The lower number of electrons at 3% CH₄ –97% H₂ was attributed to the formation of the non-diamond phase, which etched faster than diamond, resulting in a lower growth rate.     

A Brief Review: The Use of L-Ascorbic Acid as a Green Reducing Agent of Graphene Oxide

The reduced form of graphene oxide (r-GO) represents a versatile precursor to obtain graphene derivatives. Graphene oxide (GO) consists of a layered material based on a carbon skeleton functionalized by different oxygen-containing groups, while r-GO is obtained by the almost complete removal of these oxygen-containing functional groups. The r-GO has mechanical, electrical, and optical properties quite similar to graphene, thus, it proves to be a convenient 2D material useful for many technological applications. Nowadays, the most important aspects to consider in producing r-GO are: (i) the possibility of obtaining the highest reduction grade; (ii) the possibility of improving the dispersion stability of the resulting graphene using surfactants; (iii) the use of environmentally friendly and inexpensive reducing agents. Consequently, the availability of effective soft-chemistry approaches based on a green reducing agent for converting GO to r-GO are strongly needed. Among the green reductants, the most suitable is L-ascorbic acid (L-aa). Different studies have revealed that L-aa can achieve C/O ratio and conductivity values comparable to those obtained by hydrazine, a typical reducing agent. These aspects could promote an effective application strategy, and for this reason, this review summarizes and analyzes, in some detail, the up-to date literature on the reduction of GO by L-aa. The results are organized according to the two most important approaches, which are the reduction in liquid-phase, and the reduction in gel-phase. Reaction mechanisms and different experimental parameters affecting the processes were also compared.     

Dependence of the Surface Morphology and Micromechanical and Sclerometric Properties of Al2O3 Layers on the Parameters of Anodizing Aluminum Alloy

The article presents the dependence of the morphology as well as micromechanical and sclerometric properties of Al₂O₃ layers on the parameters of anodizing of aluminum alloys. The oxide layers were produced on the EN AW-5251 aluminum alloy by means of a direct current anodizing in a three-component electrolyte. The input variables (current density and electrolyte temperature) were selected based on the overall design of the experiment. The current density was 1, 2, 3 A/dm², and the electrolyte temperature was 283, 293, 303 K. The surface morphology was examined using a scanning electron microscope (SEM), and then the microscopic images were analyzed using a graphics program. The micromechanical and sclerometric properties were examined by determining the H_IT hardness and three critical loads: Lc1 (critical load at which the first damage of the tested layers occurred-Hertz tensile cracks inside the crack), Lc2 (critical load at which the first cohesive damage of the layers occurred) and Lc3 (load at which the layers were completely damaged). Sclerometric tests with the use of scratch tests were supplemented with pictures from a scanning microscope, showing the scratches. The produced layers are characterized by a hardness above 3 GPa and a porosity of 4.9–10.3%. Such a range of porosity of the produced layers allows their wide application, both for sliding associations with polymers and for their modification.     

Fluorinated Siloxane Modified Layered Double Hydroxide Sealing Film to Enhance the Corrosion Resistance of Anodic Oxide Film of Fricition Stir Welding Joint of Aluminum Alloys

Aluminum alloys and their welding structures have been widely used in aviation, aerospace, automobiles, ships, and other industrial fields. The non-uniform nature of welding structures of aluminum alloys causes intractable corrosion problems. Anodizing and subsequent sealing processes are common and effective methods to improve the corrosion resistance of welding structures. However, traditional sealing processes like hot water sealing and potassium dichromate sealing are criticized due to energy consumption or toxicity. In this work, a layered double hydroxide (LDH) sealing process with subsequent fluorinated siloxane modification is proposed to improve the corrosion resistance of the anodic oxide film of friction stir welding joints of typical aluminum alloys. The obtained sealing film with typical lamelliform structures of LDH grows well at the defects of oxidation film and also smoothens the sample surface. The hydrophobicity of the film can separate the corrosive medium from the sample surface and further enhance corrosion resistance. As a result, the corrosion current of the welded sample in 3.5 wt.% NaCl solution plummets about 3~4 orders of magnitude compared to the initial state without anodizing, indicating superior corrosion resistance brought by this method.     

Characterization of Hydroxyapatite Film Obtained by Er:YAG Pulsed Laser Deposition on Sandblasted Titanium: An In Vitro Study

The surface of titanium (Ti) dental implants must be modified to improve their applicability, owing to the biological inertness of Ti. This study aims to use sandblasting as a pretreatment method and prepare a hydroxyapatite (HA) coating on Ti to improve its biocompatibility and induce bone bonding and osteogenesis. In this paper, sandblasted Ti discs were coated with α-tricalcium phosphate (α-TCP) via Er:YAG pulsed laser deposition (Er:YAG-PLD). An HA coating was then obtained via the hydrothermal treatment of the discs at 90 °C for 10 h. The surface characteristics of the samples were evaluated by SEM, SPM, XPS, XRD, FTIR, and tensile tests. Rat bone marrow mesenchymal stem cells were seeded on the HA-coated discs to determine cellular responses in vitro. The surface characterization results indicated the successful transformation of the HA coating with a nanorod-like morphology, and its surface roughness increased. In vitro experiments revealed increased cell attachment on the HA-coated discs, as did the cell morphology of fluorescence staining and SEM analysis; in contrast, there was no increase in cell proliferation. This study confirms that Er:YAG-PLD could be used as an implant surface-modification technique to prepare HA coatings with a nanorod-like morphology on Ti discs.     

Hydroxyapatite Film Coating by Er:YAG Pulsed Laser Deposition Method for the Repair of Enamel Defects

There are treatments available for enamel demineralization or acid erosion, but they have limitations. We aimed to manufacture a device that could directly form a hydroxyapatite (HAp) film coating on the enamel with a chairside erbium-doped yttrium aluminum garnet (Er:YAG) laser using the pulsed laser deposition (PLD) method for repairing enamel defects. We used decalcified bovine enamel specimens and compacted α-tricalcium phosphate (α-TCP) as targets of Er:YAG-PLD. With irradiation, an α-TCP coating layer was immediately deposited on the specimen surface. The morphological, mechanical, and chemical characteristics of the coatings were evaluated using scanning electron microscopy (SEM), scanning probe microscopy (SPM), X-ray diffractometry (XRD), and a micro-Vickers hardness tester. Wear resistance, cell attachment of the HAp coatings, and temperature changes during the Er:YAG-PLD procedure were also observed. SEM demonstrated that the α-TCP powder turned into microparticles by irradiation. XRD peaks revealed that the coatings were almost hydrolyzed into HAp within 2 days. Micro-Vickers hardness indicated that the hardness lost by decalcification was almost recovered by the coatings. The results suggest that the Er:YAG-PLD technique is useful for repairing enamel defects and has great potential for future clinical applications.     

The Effect of the Activation Process and Metal Oxide Addition (CaO,MgO, SrO) on the Catalytic and Physicochemical Properties of Natural Zeolite in Transesterification Reaction

This work provides valuable information about unexplored catalytic systems tested in the transesterification reaction of vegetable oil with methanol. It was demonstrated that natural zeolite treatment leads to enhanced catalytic activity and yield of biodiesel production. The activation of the catalytic material in a mixture of 5% H₂–95% Ar resulted in an improvement of the values of the TG conversion and fatty acid methyl esters (FAME) yield. In addition, it was proven that the incorporation of CaO, MgO and SrO oxides onto the natural zeolite surface improves the TG conversion and FAME yield values in the transesterification reaction.     

Influence of Anodizing Parameters on Tribological Properties and Wettability of Al2O3 Layers Produced on the EN AW-5251 Aluminum Alloy

The article presents the effect of anodizing parameters of the EN AW-5251 aluminum alloy on the thickness and roughness of Al₂O₃ layers as well as their wettability and tribological properties in a sliding combination with the T7W material. The input variables were the current density of 1, 2, 3 A/dm² and the electrolyte temperature of 283, 293, 303 K. The tribological tests were performed on the T-17 tester in reciprocating motion, in conditions of technically dry friction. The tests were carried out on a 15 km road with a constant average slip speed of 0.2 m/s and a constant unit pressure of 1 MPa. The measurement of the wettability of the layers was performed using the sitting drop method, determining the contact angles on the basis of which the surface free energy was calculated. The profilographometric measurements were made. The analysis of the test results showed that the anodizing parameters significantly affect the thickness of the Al₂O₃ layers. The performed correlation analysis also showed a significant relationship between the roughness parameters and the wettability of the surface of the layers, which affects the ability to create and maintain a sliding film, which in turn translates into sliding resistance and wear of the T7W material. The analysis of friction and wear tests showed that the layer with hydrophobic properties produced at a current density of 1 A/dm² in an electrolyte at a temperature of 283 K is the most favorable for sliding associations with T7W material.     

Effect of Varying Working Distances between Sandblasting Device and Composite Substrate Surface on the Repair Bond Strength

This study investigates the effect of defined working distances between the tip of a sandblasting device and a resin composite surface on the composite–composite repair bond strength. Resin composite specimens (Ceram.x Spectra ST (HV); Dentsply Sirona, Konstanz, Germany) were aged by thermal cycling (5000 cycles, 5–55 °C) and one week of water storage. Mechanical surface conditioning of the substrate surfaces was performed by sandblasting with aluminum oxide particles (50 µm, 3 bar, 10 s) from varying working distances of 1, 5, 10, and 15 mm. Specimens were then silanized and restored by application of an adhesive system and repair composite material (Ceram.x Spectra ST (HV)). In the negative control group, no mechanical surface pretreatment or silanization was performed. Directly applied inherent increments served as the positive control group (n = 8). After thermal cycling of all groups, microtensile repair bond strength was assessed, and surfaces were additionally characterized using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). The negative control group reached the significantly lowest microtensile bond strength of all groups. No significant differences in repair bond strength were observed within the groups with varying sandblasting distances. Composite surfaces sandblasted from a distance of 1 mm or 5 mm showed no difference in repair bond strength compared to the positive control group, whereas distances of 10 or 15 mm revealed significantly higher repair bond strengths than the inherent incremental bond strength (positive control group). In conclusion, all sandblasted test groups achieved similar or higher repair bond strength than the inherent incremental bond strength, indicating that irrespective of the employed working distance between the sandblasting device and the composite substrate surface, repair restorations can be successfully performed.     

The Role of the L-Arginine-Nitric Oxide Pathway for Peristalsis in the Opossum Oesophageal Body

Knudsen MA, Frøbert O, Tøttrup A. The role of the L-arginine-nitric oxide pathway for peristalsis in the opossum oesophageal body. Scand J Gastroenterol 1994;29:1083-1087.

Background: The aim of the study was to determine the effect of N^G-nitro-L-arginine (L-NNA), an inhibitor of nitric oxide (NO) synthesis, on primary peristalsis in the oesophageal body.

Methods: Peristalsis was induced by pharyngeal stroking in 14 lightly anaesthetized opossums. Oesophageal pressures were monitored with a four-channel, perfused catheter assembly and registered with external transducers 1, 4, 7, and 10 cm proximal to the oesophagogastric junction. Propagation time was the time taken for a contraction to travel between two recording sites and was determined in the proximal, middle, and distal parts of the oesophagus (propagation time between 10 and 7 cm, 7 and 4 cm, and 4 and 1 cm recording sites, respectively).

Results: L-NNA (10^-7-10^-5mol/kg) dose-dependently reduced propagation time of the contraction in the distal oesophagus from 1.13 ± 0.24 sec to 0.27 ± 0.19 sec, whereas propagation in the proximal and middle parts of the oesophagus was unaffected. JV^G-nitro-D-arginine (D-NNA; 10^-5 mol/kg) had no influence on propagation time. In animals treated with L-NNA (10^-5 mol/kg) atropine (50 μg/kg) had no influence on propagation time in any part of the oesophagus. L-Arginine (10^-4 mol/kg) had no influence on the propagation time in animals treated with L-NNA (10^-5 mol/kg) and atropine (50 μg/kg). Neither D-NNA (10^-5 mol/kg) nor L-NNA (10^-7-10^-5 mol/kg) influenced the amplitude of the contractions at any of the recording sites. In animals given L-NNA (10^-5 mol/kg) atropine (50 μg/kg) reduced the amplitude of the contraction significantly only at the distal recording site (1-cm recording site) from 62.0 ± 4.9 mmHg to 34.5 ± 5.3 mmHg. L-Arginine (10^-4 mol/kg) had no effect on the amplitude of contractions.

Conclusion: The L-arginine-NO pathway plays a role in the control of primary peristalsic contractions of the oesophagus.