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Phosphate coatings absorption

The most important uses for phosphate coatings entail sealing with oil or paint and it is therefore of interest to study absorption values. Table 15.9 compares the absorption of diacetone alcohol into coatings of widely differing thicknesses and composition despite these differences, values of 10-8-12-9g/m are obtained throughout. It is therefore evident that absorption is predominantly a surface effect and not appreciably influenced by coating thickness. [Pg.713]

Distearyl thiodipropionate Ditridecyl thiodipropionate Poly-a-methylstyrene Trixylenyl phosphate plasticizer, absorption bases Lanolin alcohol plasticizer, ABS-PC Triphenyl phosphate plasticizer, acrylate elastomers Triisononyl trimellitate plasticizer, acrylate resins Diisooctyl phthalate plasticizer, acrylic coatings Benzyl phthalate Butyl benzyl phthalate Polypropylene glycol dibenzoate plasticizer, acrylic latex 2-Pyrrolidone... [Pg.5535]

Zinc phosphate coatings resist corrosion creep which can occur underneath paint scratches. Painting should be carried out as soon as possible after the initial drying of the coating otherwise re-absorption of water may reduce paint adhesion. [Pg.1066]

Fig. 1 UV/vis absorption spectra following the aggregation of protein A coated gold nanoparticles in the presence of antiprotein A for a the control—prior to adding antiprotein A, b at 30 min, and c at 60 min. The solution contained 7.8 x 1011 gold nanoparticles/mL and 0.32 ixg/mL antiprotein A in phosphate-buffered solution at pH 7.0... Fig. 1 UV/vis absorption spectra following the aggregation of protein A coated gold nanoparticles in the presence of antiprotein A for a the control—prior to adding antiprotein A, b at 30 min, and c at 60 min. The solution contained 7.8 x 1011 gold nanoparticles/mL and 0.32 ixg/mL antiprotein A in phosphate-buffered solution at pH 7.0...
Fig. 3 Control experiments to validate the selectivity of the aggregation process. Changes in the absorption intensity at 620 nm are used to monitor the rate of aggregation of the gold nanoparticles, a Phosphate buffer solution at pH 7.0, b 0.32 mg/mL polyclonal antiprotein A, c 7.8 x 1011 protein A coated gold nanoparticles/mL, d 7.8 x 1011 protein A coated gold nanoparticles/mL and 0.6 mg/mL monoclonal antiprotein A, e 7.8 x 1011 protein A coated gold nanoparticles/mL and 0.72 mg/mL anti-albumin, and / 7.8 xlO11 protein A coated gold nanoparticles/mL and 0.32 mg/mL polyclonal antiprotein A. All experiments were carried out in phosphate-buffered solution at pH 7.0 for 2 h... Fig. 3 Control experiments to validate the selectivity of the aggregation process. Changes in the absorption intensity at 620 nm are used to monitor the rate of aggregation of the gold nanoparticles, a Phosphate buffer solution at pH 7.0, b 0.32 mg/mL polyclonal antiprotein A, c 7.8 x 1011 protein A coated gold nanoparticles/mL, d 7.8 x 1011 protein A coated gold nanoparticles/mL and 0.6 mg/mL monoclonal antiprotein A, e 7.8 x 1011 protein A coated gold nanoparticles/mL and 0.72 mg/mL anti-albumin, and / 7.8 xlO11 protein A coated gold nanoparticles/mL and 0.32 mg/mL polyclonal antiprotein A. All experiments were carried out in phosphate-buffered solution at pH 7.0 for 2 h...
The use of the cationic micellar agent CTAB (50 mM) in phosphate-borate buffer (10 mM of each salt), pH 8.6, with 10% acetonitrile was preferred because of a faster separation (about 15 min) of heroin and related substances. Because the cationic surfactant, which coats the capillary silica wall with a positively charged layer, reverses the electroosmotic flow (EOF), the voltage (-15 kV) must be applied with a reversed polarity (with the cathode at the injection point). Detection was by UV absorption at 280 nm. [Pg.167]

Fig. 10.2. Comparison of optical and hydrodynamic properties of CdTe quantum dots (2.5 nm) solubilized in water with an amphiphilic polymer (octylamine-modified polyacrylic acid) or a multidentate polymer ligand, (a) Absorption (blue curves) and fluorescence emission red curves) spectra of CdTe quantum dots with amphiphilic polymer upper) or multidentate polymer lower) coatings, (b) Dynamic light scattering size data of quantum dots with amphiphilic polymer blue curve) and multidentate polymer green curve) coatings. PL Photoluminescence, AU Arbitrary units. All samples were dissolved in phosphate buffered saline... Fig. 10.2. Comparison of optical and hydrodynamic properties of CdTe quantum dots (2.5 nm) solubilized in water with an amphiphilic polymer (octylamine-modified polyacrylic acid) or a multidentate polymer ligand, (a) Absorption (blue curves) and fluorescence emission red curves) spectra of CdTe quantum dots with amphiphilic polymer upper) or multidentate polymer lower) coatings, (b) Dynamic light scattering size data of quantum dots with amphiphilic polymer blue curve) and multidentate polymer green curve) coatings. PL Photoluminescence, AU Arbitrary units. All samples were dissolved in phosphate buffered saline...
Erythromycin formulations are highly irritant if administered by i.m. injection and are not used in horses. Many p.o. preparations of erythromycin are enteric coated to allow passage into the small intestine, where absorption is higher because of the higher pH. In horses, erythromycin stearate and erythromycin phosphate produce peak plasma concentrations faster than the ester formulations following p.o. administration. [Pg.43]

Until recently, all ferritin cores were thought to be microcrystalline and to be the same. However, x-ray absorption spectroscopy, Mossbauer spectroscopy, and high-resolution electron microscopy of ferritin from different sources have revealed variations in the degree of structural and magnetic ordering and/or the level of hydration. Structural differences in the iron core have been associated with variations in the anions present, e.g., phosphate or sulfate, and with the electrochemical properties of iron. Anion concentrations in turn could reflect both the solvent composition and the properties of the protein coat. To understand iron storage, we need to define in more detail the relationship of the ferritin protein coat and the environment to the redox properties of iron in the ferritin core. [Pg.15]

Nowadays, the use of the reflection electron microscope (REM) or, recently, the tunnel electron microscope, as well as secondary ion mass spectrometry (SIMS), AES, electron-dispersive X-ray spectrometry, impedance spectroscopy, and so on, are yielding substantial increases in the knowledge of corrosion reactions in coatings and at their interface with metal or other substrates. As far as zinc or zinc-coated surfaces are concerned, problems of interfacial and intercoat adhesion, differential diffusion phenomena and electrolytic cell behavior on the substrate, and interreactions of zinc with conversion coatings (chromates, phosphates, silanes, silanols, etc.) have been analyzed, leading toward spectacular improvements in, for example, paint adhesion, absorption of conversion coatings and, in general, the protective action inside films as well as on their substrates. [Pg.96]


See other pages where Phosphate coatings absorption is mentioned: [Pg.714]    [Pg.743]    [Pg.358]    [Pg.605]    [Pg.351]    [Pg.181]    [Pg.47]    [Pg.190]    [Pg.267]    [Pg.28]    [Pg.622]    [Pg.493]    [Pg.186]    [Pg.493]    [Pg.29]    [Pg.346]    [Pg.488]    [Pg.18]    [Pg.486]    [Pg.620]    [Pg.358]    [Pg.64]    [Pg.8]    [Pg.248]    [Pg.325]    [Pg.350]    [Pg.351]    [Pg.48]    [Pg.441]    [Pg.190]    [Pg.1465]    [Pg.190]    [Pg.95]    [Pg.622]    [Pg.274]    [Pg.305]   
See also in sourсe #XX -- [ Pg.15 , Pg.29 ]

See also in sourсe #XX -- [ Pg.15 , Pg.29 ]




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