An XPS study of hexagonal polyoxymethylene with various bulk morphologies: surface modification under X-ray exposure

Polymer ◽  
1988 ◽  
Vol 29 (5) ◽  
pp. 797-801 ◽  
Author(s):  
P. Boulanger ◽  
J. Riga ◽  
J. Delhalle ◽  
J.J. Verbist
Keyword(s):  
X Ray ◽  
Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 806
Author(s):  
Michalina Ehlert ◽  
Aleksandra Radtke ◽  
Katarzyna Roszek ◽  
Tomasz Jędrzejewski ◽  
Piotr Piszczek

The surface modification of titanium substrates and its alloys in order to improve their osseointegration properties is one of widely studied issues related to the design and production of modern orthopedic and dental implants. In this paper, we discuss the results concerning Ti6Al4V substrate surface modification by (a) alkaline treatment with a 7 M NaOH solution, and (b) production of a porous coating (anodic oxidation with the use of potential U = 5 V) and then treating its surface in the abovementioned alkaline solution. We compared the apatite-forming ability of unmodified and surface-modified titanium alloy in simulated body fluid (SBF) for 1–4 weeks. Analysis of the X-ray diffraction patterns of synthesized coatings allowed their structure characterization before and after immersing in SBF. The obtained nanolayers were studied using Raman spectroscopy, diffuse reflectance infrared Fourier transform spectroscopy (DRIFT), and scanning electron microscopy (SEM) images. Elemental analysis was carried out using X-ray energy dispersion spectroscopy (SEM EDX). Wettability and biointegration activity (on the basis of the degree of integration of MG-63 osteoblast-like cells, L929 fibroblasts, and adipose-derived mesenchymal stem cells cultured in vitro on the sample surface) were also evaluated. The obtained results proved that the surfaces of Ti6Al4V and Ti6Al4V covered by TiO2 nanoporous coatings, which were modified by titanate layers, promote apatite formation in the environment of body fluids and possess optimal biointegration properties for fibroblasts and osteoblasts.


2013 ◽  
Vol 85 (20) ◽  
pp. 9556-9563 ◽  
Author(s):  
Annemie Adriaens ◽  
Paul Quinn ◽  
Sergey Nikitenko ◽  
Mark G. Dowsett

2001 ◽  
Vol 114-116 ◽  
pp. 307-311 ◽  
Author(s):  
José E. Gonçalves ◽  
Sandra C. Castro ◽  
Aline Y. Ramos ◽  
Maria C.M. Alves ◽  
Yoshitaka Gushikem

Langmuir ◽  
2020 ◽  
Vol 36 (37) ◽  
pp. 10923-10932
Author(s):  
Nanako Sakata ◽  
Yoshihiro Takeda ◽  
Masaru Kotera ◽  
Yasuhito Suzuki ◽  
Akikazu Matsumoto

2020 ◽  
Vol 1 (1) ◽  
pp. 1-4

Todays, researchers are challenging with manufacturing polymeric nanocomposites reinforced with ceramic particles due to two inherent properties of ceramic reinforcement particles, particle agglomeration and incompatibility between hydrophilic ceramic particles and hydrophobic polymeric matrix. So in this study, we used nano-Hydroxyapatite (n-HA) as ceramic material and Stearic acid as amphiphilic material for coating n-HA, hydroxysteric acid (SA) surfactant was used for surface coating particles between the hydrophilic HA powders and the hydrophobic polymers. The surface modification and effect of this method were evaluated by by Fourier transformation infrared (FTIR), x-ray diffractometer (XRD), thermal gravimetric analysis (TGA) and Scanning electron microscopy (SEM). The result of FTIR showed that n-HA surfaces were modified successfully and the modification method had the proper grafting amount according to TGA due to this method of modification will be proper for coating reinforcement particles in polymeric matrix.


2018 ◽  
Vol 65 (3) ◽  
pp. 249-262 ◽  
Author(s):  
Zahra Shams Ghahfarokhi ◽  
Mojtaba Bagherzadeh ◽  
Ebrahim Ghiamati Yazdi ◽  
Abbas Teimouri

Purpose The purpose of this paper is study of the type of functional group and its situation on phenyl molecule, in increasing the corrosion protection of modified graphene layers by it. Corrosion protection efficiency of graphene was raised via modifying the surface of graphene-coated carbon steel (CS/G) by using aromatic molecules. Phenyl groups with three different substitutions including COOH, NO2 and CH3 grafted to graphene via diazonium salt formation route, by using carboxy phenyl, nitro phenyl and methyl phenyl diazonium salts in ortho, meta and para spatial situations. Design/methodology/approach Molecular bindings were characterized by using X-ray diffractometer, fourier-transform infrared spectroscopy (FTIR), Raman and scanning electron microscopy (SEM)/ energy dispersive X-ray analysis (EDXA) methods. Anti-corrosion performance of modified CS/G electrodes was evaluated by weight loss and electrochemical techniques, potentiodynamic polarization (Tafel) and electrochemical impedance spectroscopy, in 3.5 per cent NaCl solution. Findings The obtained results confirmed covalently bonding of phenyl groups to the graphene surface. Also, the observed results showed that substitution spatial situations on phenyl groups can affect charge transfer resistance (Rct), corrosion potential (Ecorr), corrosion current density (jcorr) and the slope of the anodic and cathodic reaction (ßa,c), demonstrating that the proposed modification method can hinder the corrosion reactions. The proposed modification led to restoring the graphene surface defects and consequently increasing its corrosion protection efficiency. Originality/value The obtained results from electrochemical methods proved that protection efficiency was observed in order COOH < NO2 < CH3 and MPD in the para spatial situation and showed the maximum protection efficiency of 98.6 per cent in comparison to other substitutions. Finally, the ability of proposed graphene surface modification route was further proofed by using surface methods, i.e. SEM and EDXA, and contact angles measurements.


1943 ◽  
Vol 21b (2) ◽  
pp. 21-33
Author(s):  
L. A. Munro ◽  
D. J. Dewar ◽  
S. Gertsman ◽  
G. Monteith

The effect of gel water content on the catalytic activity of alumina in the decomposition of formic acid at 215 and 250 °C. has been investigated. The previous observations on the dehydration of ethyl alcohol to ether and ethylene are paralleled by the results with formic acid. There are two peaks in the curves showing the relation between activity and gel water content. The ratio CO/CO2 changes with gel water content, i.e., the course of the reaction can be altered by surface modification of the catalyst. The gel showing maximum catalytic activity exhibits greatest sorption. The temperature of activation of a hydrous oxide is not as accurate a measure of the catalytic power as the gel water content. X-ray studies of the catalysts show a threefold change in the structure in the 36 to 0% range of water content, but the fibril structure of the gel of maximum activity (5.3% water) is the same as that for minimum activity. An explanation is suggested.


2020 ◽  
Vol 7 ◽  
Author(s):  
Farnaz Ghorbani ◽  
Melika Sahranavard ◽  
Zohre Mousavi Nejad ◽  
Dejian Li ◽  
Ali Zamanian ◽  
...  

In this study, bioactive glass nanoparticles (BGNPs) with an average diameter of less than 10 nm were synthesized using a sol-gel method and then characterized by transmission electron microscopy (TEM), differential scanning calorimetric (DSC), Fourier transforms infrared spectroscopy (FTIR), and x-ray spectroscopy (XRD). Afterward, three dimensional (3D)-printed polycaprolactone (PCL) scaffolds along with fused deposition modeling (FDM) were incorporated with BGNPs, and the surface of the composite constructs was then functionalized by coating with the gelatin methacryloyl (GelMA) under UV irradiation. Field emission scanning electron microscopy micrographs demonstrated the interconnected porous microstructure with an average pore diameter of 260 µm and homogeneous distribution of BGNPs. Therefore, no noticeable shrinkage was observed in 3D-printed scaffolds compared with the computer-designed file. Besides, the surface was uniformly covered by GelMA, and no effect of surface modification was observed on the microstructure while surface roughness increased. The addition of the BGNPs the to PCL scaffolds showed a slight change in pore size and porosity; however, it increased surface roughness. According to mechanical analysis, the compression strength of the scaffolds was increased by the BGNPs addition and surface modification. Also, a reduction was observed in the absorption capacity and biodegradation of scaffolds in phosphate-buffered saline media after the incorporation of BGNPs, while the presence of the GelMA layer increased the swelling potential and stability of the composite matrixes. Moreover, the capability of inducing bio-mineralization of hydroxyapatite-like layers, as a function of BGNPs content, was proven by FE-SEM micrographs, EDX spectra, and x-ray diffraction spectra (XRD) after soaking the obtained samples in concentrated simulated body fluid. A higher potential of the modified constructs to interact with the aqueous media led to better precipitation of minerals. According to in-vitro assays, the modified scaffolds can provide a suitable surface for the attachment and spreading of the bone marrow mesenchymal stem cells (BMSCs). Furthermore, the number of the proliferated cells confirms the biocompatibility of the scaffolds, especially after a modification process. Cell differentiation was verified by alkaline phosphatase activity as well as the expression of osteogenic genes such as osteocalcin and osteopontin. Accordingly, the scaffolds showed an initial potential for reconstruction of the injured bone.


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