Influence of surface morphology and surface free energy on the anticoagulant properties of nanocone‐shaped ZnO films

2021 ◽  
pp. 52005
Author(s):  
Zhen Hong ◽  
Xingxing Yu ◽  
Hanwen Jiang ◽  
Mingshan Xue ◽  
Sibo Peng ◽  
...  
2006 ◽  
Vol 20 (4) ◽  
pp. 307-311 ◽  
Author(s):  
Emilena Maria Castor Xisto Lima ◽  
Wander José da Silva ◽  
Juliana Silva Moura ◽  
Fernanda Faot ◽  
Altair Antoninha Del Bel Cury

The aim of this study was to evaluate surface free energy (SFE), surface roughness (SR) and surface hardness (SH) of two commercially available materials for fabricating dental implant abutments. In addition, the specimens were investigated by scanning electron microscopy (SEM) to determine the surface morphology. Twenty five discs (5 x 2 mm) of Ti-6Al-4V and Tilite (Ni-Cr-Ti) alloys were used in this study. Surface free energy was determined by the contact angle formed between a drop of distilled, deionized water and the surface of the specimen of each material. The surface roughness was measured with a mechanical profilometer and the surface hardness was evaluated by means of the Vickers hardness micro indentation test. SFE, SR and SH data were analyzed using one-way ANOVA (p < 0.05). Statistical differences (p < 0.05) were found between Ti-6Al-4V (36.2 erg.cm-2; 0.2 µm) and Tilite (30.9 erg.cm-2; 0.16 µm) for SFE and SR. However, the differences between the surface hardness values of Ti-6Al-4V (325.0 kg/mm²) and Tilite (324.3 kg/mm²) were not statistically significant (p > 0.05). Evaluations by SEM revealed different surface morphology. Within the limits of this study, it can be concluded that the Ti-6Al-4V and Tilite alloys showed differences in surface properties, except for surface hardness, suggesting that both alloys may be considered appropriate for producing abutments. Further studies are, however, necessary to elucidate the biological responses to implant abutments made with these alloys.


2012 ◽  
Vol 717-720 ◽  
pp. 633-636 ◽  
Author(s):  
Biplob K. Daas ◽  
Kevin M. Daniels ◽  
S. Shetu ◽  
Tangali S. Sudarshan ◽  
M.V.S. Chandrashekhar

We present epitaxial graphene (EG) growth on non-polar a-plane and m-plane 6H-SiC faces where material characterization is compared with that known for EG grown on polar faces. AFM surface morphology exhibits nanocrystalline graphite like features for non-polar faces, while polar silicon face shows step like features. This differing behavior is attributed to the lack of a hexagonal template on the non-polar faces. Non-polar faces also exhibit greater disorder and red shift of all Raman peaks (D, G and 2D) with increasing temperature. This is attributed to decreasing stress with increasing temperature. These variations provide evidence of different EG growth mechanisms on non-polar and polar faces, likely due to differences in surface free energy. We also present differences between a-plane ( ) EG and m-plane ( ) EG in terms of morphology, thickness and Raman characteristics.


1989 ◽  
Vol 50 (24) ◽  
pp. 3527-3534 ◽  
Author(s):  
P. Oswald ◽  
F. Melo ◽  
C. Germain

2011 ◽  
Vol 2 (2) ◽  
pp. 101-105
Author(s):  
L. Fazekas ◽  
Z. S. Tiba ◽  
G. Kalácska

Abstract The lubricant storing and releasing ability of the thermally sprayed surfaces plays an essential role in the proper operation of the components. In the case of porous sprayed surfaces the lubricant storing and releasing ability depends mainly on porosity and the surface energy (adhesion susceptibility). The adhesion ability can also be expressed indirectly with an index number that is by determining the surface free energy.


1989 ◽  
Vol 54 (12) ◽  
pp. 3171-3186 ◽  
Author(s):  
Jan Kloubek

The validity of the Fowkes theory for the interaction of dispersion forces at interfaces was inspected for the system water-aliphatic hydrocarbons with 5 to 16 C atoms. The obtained results lead to the conclusion that the hydrocarbon molecules cannot lie in a parallel position or be randomly arranged on the surface but that orientation of molecules increases there the ration of CH3 to CH2 groups with respect to that in the bulk. This ratio is changed at the interface with water so that the surface free energy of the hydrocarbon, γH, rises to a higher value, γ’H, which is effective in the interaction with water molecules. Not only the orientation of molecules depends on the adjoining phase and on the temperature but also the density of hydrocarbons on the surface of the liquid phase changes. It is lower than in the bulk and at the interface with water. Moreover, the volume occupied by the CH3 group increases on the surface more than that of the CH2 group. The dispersion component of the surface free energy of water, γdW = 19.09 mJ/m2, the non-dispersion component, γnW = 53.66 mJ/m2, and the surface free energies of the CH2 and CH3 groups, γ(CH2) = 32.94 mJ/m2 and γ(CH3) = 15.87 mJ/m2, were determined at 20 °C. The dependence of these values on the temperature in the range 15-40 °C was also evaluated.


2020 ◽  
Vol 7 (12) ◽  
pp. 3869-3876
Author(s):  
Kathryn M. Peruski ◽  
Brian A. Powell

Solubility of neptunium dioxide decreases as microstructure grain size increases, likely due to decreasing surface free energy and surface area.


2021 ◽  
pp. 002203452110181
Author(s):  
A.A. Balhaddad ◽  
I.M. Garcia ◽  
L. Mokeem ◽  
M.S. Ibrahim ◽  
F.M. Collares ◽  
...  

Cervical composites treating root carious and noncarious cervical lesions usually extend subgingivally. The subgingival margins of composites present poor plaque control, enhanced biofilm accumulation, and cause gingival irritation. A potential material to restore such lesions should combine agents that interfere with bacterial biofilm development and respond to acidic conditions. Here, we explore the use of new bioresponsive bifunctional dental composites against mature microcosm biofilms derived from subgingival plaque samples. The designed formulations contain 2 bioactive agents: dimethylaminohexadecyl methacrylate (DMAHDM) at 3 to 5 wt.% and 20 wt.% nanosized amorphous calcium phosphate (NACP) in a base resin. Composites with no DMAHDM and NACP were used as controls. The newly formulated 5% DMAHDM–20% NACP composite was analyzed by micro-Raman spectroscopy and transmission electron microscopy. The wettability and surface-free energy were also assessed. The inhibitory effect on the in vitro biofilm growth and the 16S rRNA gene sequencing of survival bacterial colonies derived from the composites were analyzed. Whole-biofilm metabolic activity, polysaccharide production, and live/dead images of the biofilm grown over the composites complement the microbiological assays. Overall, the designed formulations had higher contact angles with water and lower surface-free energy compared to the commercial control. The DMAHDM-NACP composites significantly inhibited the growth of total microorganisms, Porphyromonas gingivalis, Prevotella intermedia/nigrescens, Aggregatibacter actinomycetemcomitans, and Fusobacterium nucleatum by 3 to 5-log ( P < 0.001). For the colony isolates from control composites, the composition was typically dominated by the genera Veillonella, Fusobacterium, Streptococcus, Eikenella, and Leptotrichia, while Fusobacterium and Veillonella dominated the 5% DMAHDM–20% NACP composites. The DMAHDM-NACP composites contributed to over 80% of reduction in metabolic and polysaccharide activity. The suppression effect on plaque biofilms suggested that DMAHDM-NACP composites might be used as a bioactive material for cervical restorations. These results may propose an exciting path to prevent biofilm growth and improve dental composite restorations’ life span.


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