The fundamental corrosion behavior of silicon carbide (SIC) ceramics was investigated after immersion in 290°C water solutions with different pH and dissolved-oxygen concentrations. The weight loss in the oxygenated solution was more than that in the deoxygenated solution and was accelerated by increasing pH. Preferential attack could be found at grain boundaries and around pores on the sample surface immersed in the oxygenated alkaline solution. The weight change, dw, followed the general rate law, (dW)" = kt. The exponent, m , was 1.11 in the alkaline solution and 0.45 in the acidic solution. Based on the above results, the Sic was considered to be directly hydrolyzed to a silica sol, with its dissolution kinetics dependent on the sol stability. This corrosion behavior is quite different from those in high-temperature or vapor-phase hydrothermal oxidation, where the oxidation rate is controlled by oxidant diffusion through the protective silica surface layer. [
We describe attempts to achieve high throughput of 17beta-estradiol (E2) analysis, including the development of an immunocleanup membrane using polyclonal antibodies and an enzyme-linked immunosorbent assay (ELISA) using monoclonal antibodies. An epoxy-group-containing monomer, glycidyl methacrylate (GMA), was graft-polymerized onto a porous hollow-fiber membrane. Subsequently, anti-estrogen (ES) antibody, as a ligand, was coupled with the epoxy group. The ligand density ranged from 3.1 to 5.8 mg/g of the GMA-grafted porous hollow-fiber membrane. A 1.0 microg/L E2 solution was forced to permeate through pores rimmed by the anti-ES-antibody-immobilized polymer chains, at a constant permeation rate. A breakthrough curve, that is, the change in the E2 concentration of the effluent penetrating the outside of the hollow fiber with a change of the effluent volume, was determined. Bound E2 in amounts ranging from 0.42 to 0.80 microg was quantitatively eluted with 3-5 mL of methanol in the permeation mode. The higher permeation rate of the E2 solution resulted in the higher overall binding rate of E2 to the anti-ES-antibody-immobilized porous hollow-fiber membrane because of the negligible diffusional mass-transfer resistance of E2 to the antibody.
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