SynopsisZone centrifugation experiments are occasionally ruined by convective processes which occur a t one gravity subsequent to layering a solution of macromolecules on a supporting density gradient. The factors which contribute to this convection have been little understood. In most of the experiments described in this communication, Blue Dextran 2000 is used as the macromolecular component. The convective disturbance may be clearly seen and accurately measured. The effects of macromolecular concentration, composition and density of the supporting gradient, diffusion coefficient of the solute, and several other variables are studied, and an empirical equation constructed to describe the phenomenon. T h i s convective disturbance appears to be minimized or prevented by layering and fractionating in the presence of a centrifugal field.When a solution of large molecules is layered at one gravity over a more dense solution containing a low molecular weight solute, small streaming columns of the macromolecular solution may form at the interface and sink through the dense solution below. An understanding of the conditions governing this phenomenon is important for zone centrifugation studies.In this communication, we will examine some of the factors upon which the convective disturbance depends. In order to do this, a measurement of some reproducible quantity associated with the streaming phenonemon is required. It has proven to be convenient to measure the time interval which occurs after layering, but before the formation of streaming columns of macromolecules. This time lag may be determined with some precision. By showing how the time lag varies with concentration, diffusion coefficient, temperature, etc., we may determine those parameters of the system which are critically involved in the initiation of the streaming phenomenon.
A biosensor is an electronic device that measures biologically important parameters. An example is a sensor that measures the chemicals and materials released during corrosion of a biodegradable magnesium implant that impact surrounding cells, tissues and organs. A responsive biosensor is a biosensor that responds to its own measurements. An example is a sensor that measures the corrosion of an implant and automatically adjusts (slows down or speeds up) the corrosion rate. The University of Cincinnati, the University of Pittsburgh, North Carolina A&T State University, and the Hannover Medical Institute are collaborators in an NSF Engineering Research Center (ERC) for Revolutionizing Metallic Biomaterials (RBM). The center will use responsive sensors in experimental test beds to develop biodegradable magnesium implants. Our goal is to develop biodegradable implants that combine novel bioengineered materials based on magnesium alloys, miniature sensor devices that monitor and control the corrosion, and coatings that slow corrosion and release biological factors and drugs that will promote healing in surrounding tissues. Responsive biosensors will monitor what is happening at the interface between the implant and tissue to ensure that the implant is effective, biosafe, and provides appropriate strength while degrading. Corrosion behavior is a critical factor in the design of the implant. The corrosion behavior of implants will be studied using biosensors and through mathematical modeling. Design guidelines will be developed to predict the degradation rate of implants, and to predict and further study toxicity arising from corrosion products (i.e., Mg ion concentrations, pH levels, and hydrogen gas evolution). Knowing the corrosion rate will allow estimations to be made of implant strength and toxicity risk throughout the degradation process.
Anodization is known to be an effective way to slow down the initial corrosion rate of magnesium (Mg) and its alloys. Here, we investigated the specific use of oxy-salts to improve the corrosion resistance of anodizing coatings. Oxy-salts of silicate, phosphate, and carbonate were added separately to a sodium hydroxide alkaline electrolyte used to anodize Mg alloy AZ91D. The process was investigated in terms of anodizing behavior, the surface properties, and the corrosion behavior of AZ91D. Anodizing AZ91D using the silicate-containing electrolyte generated sparks, and produced a thicker and more corrosion-resistant layer than the other oxy-salts. In the process, MgO and SiO2 formed Mg2SiO4 at high temperatures. Coatings from the phosphate-and carbonate-containing electrolyte anodizations did not contain phosphorus or carbon. We also studied the effects of silicate concentration on the corrosion resistance and properties of the surface.
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