Understanding the corrosion behavior of amorphous multiple-layer carbon coating

Calcium is supposed to play an important role in the control of protoplasmic streaming in slime mold plasmodia. The motive force for protoplasmic streaming is generated by the interaction of actin and myosin. This contraction is supposed to be controlled by intracellular Ca-fluxes similar to the triggering system in skeleton muscle. The histochemical localisation of calcium however is problematic because of the possible diffusion artifacts especially in aquous media.To evaluate this problem calcium localisation was studied in small pieces of shock frozen (liquid propane at -189°C) plasmodial strands of Physarum polycephalum, which were further processed with 3 different methods: 1) freeze substitution in ethanol at -75°C, staining in 100% ethanol with 1% uranyl acetate, and embedding in styrene-methacrylate. For comparison the staining procedure was omitted in some preparations. 2)Freeze drying at about -95°C, followed by immersion with 100% ethanol containing 1% uranyl acetate, and embedding. 3) Freeze fracture, carbon coating and SEM investigation at temperatures below -100° C.

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Sem Studies of Co-Cr-Mo Surgical Implant Alloy Corrosion Behavior

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100055448 ◽

1982 ◽

Vol 40 ◽

pp. 520-521

Author(s):

Ann Chidester Van Orden ◽

John L. Chidester ◽

Anna C. Fraker ◽

Pei Sung

Keyword(s):

Electron Microscopy ◽

Corrosion Behavior ◽

Anodic Polarization ◽

Saline Solution ◽

Saturated Calomel Electrode ◽

Physiological Saline ◽

X Ray ◽

Physiological Saline Solution ◽

Scanning Electron

The influence of small variations in the composition on the corrosion behavior of Co-Cr-Mo alloys has been studied using scanning electron microscopy (SEM), energy dispersive x-ray analysis (EDX), and electrochemical measurements. SEM and EDX data were correlated with data from in vitro corrosion measurements involving repassivation and also potentiostatic anodic polarization measurements. Specimens studied included the four alloys shown in Table 1. Corrosion tests were conducted in Hanks' physiological saline solution which has a pH of 7.4 and was held at a temperature of 37°C. Specimens were mechanically polished to a surface finish with 0.05 µm A1203, then exposed to the solution and anodically polarized at a rate of 0.006 v/min. All voltages were measured vs. the saturated calomel electrode (s.c.e.).. Specimens had breakdown potentials near 0.47V vs. s.c.e.

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Surface Structure in Microtomed Sections Caused by Glass and Diamond Knives

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100066334 ◽

1971 ◽

Vol 29 ◽

pp. 456-457

Author(s):

J. Temple Black ◽

William G. Boldosser

Keyword(s):

Plastic Deformation ◽

Epoxy Resin ◽

Carbon Coating ◽

Surface Damage ◽

Body Angle ◽

Normal Manner ◽

Bottom Side ◽

Cutting Direction ◽

Made In ◽

Diamond Knife

Ultramicrotomy produces plastic deformation in the surfaces of microtomed TEM specimens which can not generally be observed unless special preparations are made. In this study, a typical biological composite of tissue (infundibular thoracic attachment) infiltrated in the normal manner with an embedding epoxy resin (Epon 812 in a 60/40 mixture) was microtomed with glass and diamond knives, both with 45 degree body angle. Sectioning was done in Portor Blum Mt-2 and Mt-1 microtomes. Sections were collected on formvar coated grids so that both the top side and the bottom side of the sections could be examined. Sections were then placed in a vacuum evaporator and self-shadowed with carbon. Some were chromium shadowed at a 30 degree angle. The sections were then examined in a Phillips 300 TEM at 60kv.Carbon coating (C) or carbon coating with chrom shadowing (C-Ch) makes in effect, single stage replicas of the surfaces of the sections and thus allows the damage in the surfaces to be observable in the TEM. Figure 1 (see key to figures) shows the bottom side of a diamond knife section, carbon self-shadowed and chrom shadowed perpendicular to the cutting direction. Very fine knife marks and surface damage can be observed.

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Specimen Preparation for Clinical Applications of X-Ray Microanalysis

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100135241 ◽

1990 ◽

Vol 48 (2) ◽

pp. 328-329

Author(s):

J.D. Shelburne ◽

G.M. Roomans

Keyword(s):

Carbon Coating ◽

Clinical Applications ◽

Point Of View ◽

Practical Significance ◽

Sweat Test ◽

Specimen Preparation ◽

Tissue Preparation ◽

X Ray ◽

Gallbladder Stones ◽

Clinical Problems

Proper preparative procedures are a prerequisite for the validity of the results of x-ray microanalysis of biological tissue. Clinical applications of x-ray microanalysis are often concerned with diagnostic problems and the results may have profound practical significance for the patient. From this point of view it is especially important that specimen preparation for clinical applications is carried out correctly.Some clinical problems require very little tissue preparation. Hair, nails, and kidney and gallbladder stones may be examined and analyzed after carbon coating. High levels of zinc or copper in hair may be indicative of dermatological or systemic diseases. Nail clippings may be analyzed (as an alternative to the more conventional sweat test) to confirm a diagnosis of cystic fibrosis. X-ray microanalysis in combination with scanning electron microscopy has been shown to be the most reliable method for the identification of the components of kidney or gallbladder stones.A quantitatively very important clinical application of x-ray microanalysis is the identification and quantification of asbestos and other exogenous particles in lung.

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