The Effect of Laser Induced Oxygen-Diffusion Hardening on the Surface Structure and Scratch Resistance of Commercially Pure Ti

2009 ◽  
pp. 649-650 ◽  
Author(s):  
Chen Changjun ◽  
Zhang Shichang ◽  
Zhang Min ◽  
Chang Qingming
2015 ◽  
Vol 630 ◽  
pp. 51-57 ◽  
Author(s):  
Helga Hornberger ◽  
Clemens Randow ◽  
Claudia Fleck

2015 ◽  
Vol 652 ◽  
pp. 012014
Author(s):  
Yu F Ivanov ◽  
A D Teresov ◽  
E A Petrikova ◽  
O V Ivanova ◽  
I A Ikonnikova

Author(s):  
Natthaphong KONKHUNTHOT ◽  
Patcharanut BURANAPIMA ◽  
Patipan BOONNITEE ◽  
Mahamasuhaimi MASAE ◽  
Peerawas KONGSONG

In the present work, pack carburization with rubberwood charcoal and rubberwood ash at 925 °C for 6, 12, and 24 h was carried out to improve the surface hardness of commercially pure titanium (CP-Ti).  X-ray diffraction and energy dispersive spectrometer analyses revealed the formation of titanium carbide (TiC) and the existence of oxygen diffusion in the carburized surface. The surface hardness of most optimized conditions has remarkably increased by 481 % as compared to untreated CP-Ti (from 175 HV to 1016 HV) due to the TiC surface layer, while the hardened oxygen diffusion layer of about 300 μm in-depth, as clearly seen in the microhardness profiles is useful for increased load-bearing capacity. Consequently, pack carburization with rubberwood charcoal and rubberwood ash is a promising surface modification technique, which can significantly enhance the surface hardness and increase the load-bearing capacity of CP-Ti for biomedical and tribological applications. HIGHLIGHTS Rubberwood charcoal and ash are a new carbon source to fabricate the TiC layer on CP-Ti. Formation of the TiC layer remarkably enhances the surface hardness of CP-Ti by 481 %. The hardened oxygen diffusion layer is beneficial to load-bearing and anti-wear capacity. GRAPHICAL ABSTRACT


Author(s):  
Sanford H. Vernick ◽  
Anastasios Tousimis ◽  
Victor Sprague

Recent electron microscope studies have greatly expanded our knowledge of the structure of the Microsporida, particularly of the developing and mature spore. Since these studies involved mainly sectioned material, they have revealed much internal detail of the spores but relatively little surface detail. This report concerns observations on the spore surface by means of the transmission electron microscope.


Author(s):  
Robert M. Glaeser ◽  
Thea B. Scott

The carbon-replica technique can be used to obtain information about cell-surface structure that cannot ordinarily be obtained by thin-section techniques. Mammalian erythrocytes have been studied by the replica technique and they appear to be characterized by a pebbly or “plaqued“ surface texture. The characteristic “particle” diameter is about 200 Å to 400 Å. We have now extended our observations on cell-surface structure to chicken and frog erythrocytes, which possess a broad range of cellular functions, and to normal rat lymphocytes and mouse ascites tumor cells, which are capable of cell division. In these experiments fresh cells were washed in Eagle's Minimum Essential Medium Salt Solution (for suspension cultures) and one volume of a 10% cell suspension was added to one volume of 2% OsO4 or 5% gluteraldehyde in 0.067 M phosphate buffer, pH 7.3. Carbon replicas were obtained by a technique similar to that employed by Glaeser et al. Figure 1 shows an electron micrograph of a carbon replica made from a chicken erythrocyte, and Figure 2 shows an enlarged portion of the same cell.


Author(s):  
S. S. Breese ◽  
H. L. Bachrach

Models for the structure of foot-and-mouth disease virus (FMDV) have been proposed from chemical and physical measurements (Brown, et al., 1970; Talbot and Brown, 1972; Strohmaier and Adam, 1976) and from rotational image-enhancement electron microscopy (Breese, et al., 1965). In this report we examine the surface structure of FMDV particles by high resolution electron microscopy and compare it with that of particles in which the outermost capsid protein VP3 (ca. 30, 000 daltons) has been split into smaller segments, two of which VP3a and VP3b have molecular weights of about 15, 000 daltons (Bachrach, et al., 1975).Highly purified and concentrated type A12, strain 119 FMDV (5 mg/ml) was prepared as previously described (Bachrach, et al., 1964) and stored at 4°C in 0. 2 M KC1-0. 5 M potassium phosphate buffer at pH 7. 5. For electron microscopy, 1. 0 ml samples of purified virus and trypsin-treated virus were dialyzed at 4°C against 0. 2 M NH4OAC at pH 7. 3, deposited onto carbonized formvar-coated copper screens and stained with phosphotungstic acid, pH 7. 3.


Sign in / Sign up

Export Citation Format

Share Document