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Hydrophobic coating tests

Simone and Popino have considered the stability of neomycin in both hydrophobic and hydrophilic ointment bases. No loss of potency over a period of 1 year at 20°C was reported for formulations containing carboxymethylcellulose, polyethylene glycol(P.E.G.) or white-soft paraffin. However, formulations containing hydrous lanolin were reported to be unstable. All materials used in the formulations were obtained from U.S. sources. Coates et al3°l investigated the use of P.E.G. from British sources and described neomycin as being incompatible with the materials tested. [Pg.425]

Once the durability testing of the fuel cells is finalized, the internal components are then characterized. For diffusion layers, some of these characterization techniques include SEM to visualize surface changes, porosimetry measurements to analyze any changes in porosity within the DL and MPL, IGC (inverse gas chromatography) to identify relative humidity effects on the hydrophobic properties of the DLs, contact angle measurements to observe any changes in the hydrophobic/hydrophilic coatings of the DL, etc. [254,255]. [Pg.278]

Through the use of x-ray-induced photoelectron spectroscopy (XPS), Schulze et al. [259] were able to demonstrate that the PTFE particles, which are coated on the diffusion layers, decomposed after fuel cell testing for more than 1,600 hours. This resulted in a change of the hydrophobic properties of the DL. Unfortunately, the mechanism behind the decomposition of PTFE was not explained. [Pg.280]

An inappropriate coating procedure for dsDNA may reduce the specificity of the test. Only ssDNA binds to the hydrophobic surfaces coated with polystyrol, the coating material generally used in ELISAs (E8). Cationic carriers for dsDNA binding, such as poly-L-lysine and protamine sulfate, may result in false-positive antibody reactions (B24). Another binder, an amphipolar ion-pair reagent, has been shown to be fully inert to immunoglobulins. [Pg.147]

In 1996, Gauglitz and coworkers coated surfaces with various amino-and carboxy-substituted polymers [198], The polymers tested were branched poly-(ethyleneimine), a,co-amino-functionalized PEG, chitosan, poly(acrylamide-co-acrylic acid) and an amino-modified dextran. The amino-substituted polymers were immobilized on glass by first immobilizing an aminosilane, followed by succinic anhydride/A-hydroxysuccinimide linker chemistry. Poly(acrylamide-co-acrylic acid) was directly coupled to an aminosilanized surface. When probed with 1 mg mL 1 ovalbumin solution, nonspecific adsorption was lowest for the dextran derivative. Notably, nonspecific adsorption increased in most cases when a hydrophobic hapten (atrazine) was coupled to the polymer-modified surface. [Pg.28]

Therefore inorganic sunscreens commonly used in cosmetic industry should be carefully tested for their photoactivity and phototoxicity. Sunscreens based on titanium and zinc oxides should contain additional antioxidants, eg a-tocopherol or j5-carotene. Even more efficient protection against unwanted ROSs can be achieved by a smart titanium dioxide modification that would block its photocatalytic activity. Recently Lee et al. described a hydrophobic multicomponent polymer coating for nanocrystalline Ti02 containing natural antioxidants extracted from grape seeds... [Pg.356]

Fifty-Microliter Samples. For small sample volumes. Durst (23) showed that with a gelled fluoride electrode in an inverted position and a conventional calomel reference electrode, the fluoride electrode could be made the sample container, and measurements can be made in samples as small as 50 juL. This concept was applied here with the chloride electrode in the inverted position because all connections in the electrode are solid state no liquids are inside the body. The fluoride electrode (Orion Model 94-09), used here as the reference, was directly opposed to the chloride electrode with an air gap of about I mm (Figure 4). Both flat membranes were lightly coated with silicone oil to make them hydrophobic, and the test solution was pipetted into the gap. [Pg.67]

One recourse is to use low-destructive test methods that can quantify the efficacy of protective agents [27] and provide evidence of improper use or application of the silicone [4, 15, 27, 28, 32, 36, 37], High-resolution microscopy would offer the advantage of visualizing the reasons for failure of hydrophobic treatments just after application, before they became visible very much later when the weathered materials started to fail [38, 39]. Weak areas such as inadequate uptake of the treatment, poor penetration depth, and incompleteness of coating could be documented just after the masonry treatment had been applied. [Pg.828]

A sample of the coating is ignited in a test tube or wet-ashed with concentrated HjSO and IINO, . This leaves a residue of silica and the glass tube will become hydrophobic to acid and water. The presence of silicon is confirmed by ... [Pg.136]

Experiments with several different hydrophobic quaternary ammonium salts as coating reagents showed that the adjusted retention times of test anions relative to t for chloride varied somewhat with the chemical structure of the coating [20]. However, it was found that the relative adjusted retention times also varied considerably... [Pg.49]


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