Scanning electron microscopy and thermal characteristics of dentin ablated by a short-pulse XeCl excimer laser

1993 ◽  
Vol 13 (3) ◽  
pp. 353-362 ◽  
Author(s):  
Joseph Neev ◽  
Adam Stabholtz ◽  
Lih-Huei L. Liaw ◽  
Mahmoud Torabinejad ◽  
Jack T. Fujishige ◽  
...  
Author(s):  
Long-Sun Chao ◽  
Yu-Ru Chen ◽  
Hsiun-Chang Peng

In this work, the excimer-laser-induced crystallization of amorphous silicon (a-Si) films was investigated numerically and experimentally. The basic structure is an a-Si film on a glass substrate. This study had investigated the effects of irradiating energy density on the grain size and structure by scanning electron microscopy (SEM). In the surface microstructure analysis of the laser-irradiated area, the critical fluences (full-melt threshold, FMT) between the partial melting and complete melting regimes can be found by applying scanning electron microscopy. An efficient two-dimensional numerical model is carried out to predict the critical fluences (FMT) and the transient temperature distribution during the laser processing. Numerical analysis of the temperature profile showed that a temperature drop occurred at the center of melted zone immediately after laser irradiation. From the analysis of temperature responses, the FMT obtained from the simulation results of the proposed model agree fairly well with those from the experimental data reported in the literature and acquired in this research. Furthermore, the grain growth of the poly-Si was studied by the grain observation of the cross section and its corresponding numerical simulation. The cross-sectional grain structure of the resulting poly-Si film was observed with different laser intensities. The grain sizes decreased with increasing irradiating energy intensity in the partial melting regime. From the surface observation, the grain distribution was uniform and most of the grain has a single crystallographic direction. The average grain size had the biggest value at FMT. But some super large grains occurred and combined with more than one crystallographic direction when the film obtained sufficiently high energy intensities that was closed or over the FMT. The grain distribution was not uniform. The super large gain was around the small grain size. The modified cellular automation method (MCA) was used to simulate the grain growth two-dimensionally and explain the grain development during the solidification process. The grain morphology of the numerical simulation was satisfied with the experimental observation. From the analysis of the grain growth, this model was able to simulate the undercooling effect and grain growth phenomenon and fitted for the experimental grain observation in the excimer-laser-induced crystallization.


2015 ◽  
Vol 78 (6) ◽  
pp. 472-478 ◽  
Author(s):  
Lívia Tosi Trevelin ◽  
Márcia Martins Marques ◽  
Ana Cecília Correa Aranha ◽  
Victor Elias Arana-Chavez ◽  
Adriana Bona Matos

2008 ◽  
Vol 47-50 ◽  
pp. 678-681 ◽  
Author(s):  
Chanakan Asasutjarit ◽  
Sarocha Charoenvai ◽  
Jongjit Hirunlabh ◽  
Joseph Khedari

The effects of pretreatment of coir fiber for manufacturing coir-based green composites have been studied. Composites were prepared using coir fiber treated with varying pretreatment condition. The process ability conditions and physical, mechanical and thermal characteristics of these composites were analyzed. The changes in morphological properties with different coir pretreatment condition were discussed. Surface characterizations of the unpretreated and pretreated coir fiber were investigated from scanning electron microscopy (SEM) studies. It revealed that there is an improved adhesion between fiber and matrix in the case of pretreated coir. SEM investigations confirm that the increase in properties is caused by improved fiber-matrix adhesion.


2005 ◽  
Vol 103 (2) ◽  
pp. 328-336 ◽  
Author(s):  
Henk Johan N. Streefkerk ◽  
Sanne Kleinveld ◽  
Ester L. G. E. Koedam ◽  
Marcel M. M. Bulder ◽  
Hans D. Meeldijk ◽  
...  

Object. In contrast to conventional anastomosis methods, the excimer laser—assisted nonocclusive anastomosis (ELANA) technique involves a platinum ring and intima—adventitia apposition with a rim of medial and adventitial layers exposed to the bloodstream. The authors assessed the reendothelialization of porcine carotid arteries through ELANA compared with conventional anastomosis by using scanning electron microscopy. Methods. In 28 pigs a bypass with one ELANA and one conventional anastomosis was made on the left common carotid artery. All patent anastomoses were evaluated intraoperatively with the aid of an ultrasonographic flowmeter and postoperatively by using scanning electron microscopy at 2 weeks, 2 months, 3 months, and 6 months thereafter. Twenty-four of 28 bypasses (48 of 56 end-to-side anastomoses) were fully patent at the time of evaluation. On scanning electron microscopic evaluation of the bypasses, all 48 patent anastomoses showed complete reendothelialization, including all 24 ELANAs in which the endothelium covered the rim and the laser-ablated edge completely. No endothelial difference was observed between conventional anastomoses and ELANAs, aside from the obvious anatomical differences like the platinum ring, which had been completely covered with endothelium. At 6 months postsurgery, remodeling of the ELANA was observed, leaving the ring covered with a layer of endothelium as the most narrow part of the anastomosis. Conclusions. In long-term experiments, ELANA allows reendothelialization comparable to that achieved with conventional anastomosis. Considering its nonocclusive and high-flow characteristics, the ELANA technique is preferable in cerebral revascularization procedures.


Author(s):  
P.S. Porter ◽  
T. Aoyagi ◽  
R. Matta

Using standard techniques of scanning electron microscopy (SEM), over 1000 human hair defects have been studied. In several of the defects, the pathogenesis of the abnormality has been clarified using these techniques. It is the purpose of this paper to present several distinct morphologic abnormalities of hair and to discuss their pathogenesis as elucidated through techniques of scanning electron microscopy.


Author(s):  
P.J. Dailey

The structure of insect salivary glands has been extensively investigated during the past decade; however, none have attempted scanning electron microscopy (SEM) in ultrastructural examinations of these secretory organs. This study correlates fine structure by means of SEM cryofractography with that of thin-sectioned epoxy embedded material observed by means of transmission electron microscopy (TEM).Salivary glands of Gromphadorhina portentosa were excised and immediately submerged in cold (4°C) paraformaldehyde-glutaraldehyde fixative1 for 2 hr, washed and post-fixed in 1 per cent 0s04 in phosphosphate buffer (4°C for 2 hr). After ethanolic dehydration half of the samples were embedded in Epon 812 for TEM and half cryofractured and subsequently critical point dried for SEM. Dried specimens were mounted on aluminum stubs and coated with approximately 150 Å of gold in a cold sputtering apparatus.Figure 1 shows a cryofractured plane through a salivary acinus revealing topographical relief of secretory vesicles.


Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).


Author(s):  
Ronald H. Bradley ◽  
R. S. Berk ◽  
L. D. Hazlett

The nude mouse is a hairless mutant (homozygous for the mutation nude, nu/nu), which is born lacking a thymus and possesses a severe defect in cellular immunity. Spontaneous unilateral cataractous lesions were noted (during ocular examination using a stereomicroscope at 40X) in 14 of a series of 60 animals (20%). This transmission and scanning microscopic study characterizes the morphology of this cataract and contrasts these data with normal nude mouse lens.All animals were sacrificed by an ether overdose. Eyes were enucleated and immersed in a mixed fixative (1% osmium tetroxide and 6% glutaraldehyde in Sorenson's phosphate buffer pH 7.4 at 0-4°C) for 3 hours, dehydrated in graded ethanols and embedded in Epon-Araldite for transmission microscopy. Specimens for scanning electron microscopy were fixed similarly, dehydrated in graded ethanols, then to graded changes of Freon 113 and ethanol to 100% Freon 113 and critically point dried in a Bomar critical point dryer using Freon 13 as the transition fluid.


Author(s):  
Jane A. Westfall ◽  
S. Yamataka ◽  
Paul D. Enos

Scanning electron microscopy (SEM) provides three dimensional details of external surface structures and supplements ultrastructural information provided by transmission electron microscopy (TEM). Animals composed of watery jellylike tissues such as hydras and other coelenterates have not been considered suitable for SEM studies because of the difficulty in preserving such organisms in a normal state. This study demonstrates 1) the successful use of SEM on such tissue, and 2) the unique arrangement of batteries of nematocysts within large epitheliomuscular cells on tentacles of Hydra littoralis.Whole specimens of Hydra were prepared for SEM (Figs. 1 and 2) by the fix, freeze-dry, coat technique of Small and Màrszalek. The specimens were fixed in osmium tetroxide and mercuric chloride, freeze-dried in vacuo on a prechilled 1 Kg brass block, and coated with gold-palladium. Tissues for TEM (Figs. 3 and 4) were fixed in glutaraldehyde followed by osmium tetroxide. Scanning micrographs were taken on a Cambridge Stereoscan Mark II A microscope at 10 KV and transmission micrographs were taken on an RCA EMU 3G microscope (Fig. 3) or on a Hitachi HU 11B microscope (Fig. 4).


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