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Spin coating procedure

The rqjroducibility of polymer film formation is greatly improved by the spin coating technique where the polymer solution is applied by a microsyringe onto the center of a rapidly rotated disk electrode Rather thick films can be produced by repeated application of small volumes of stock solution. A thorough discussion and detailed experimental description of a reliable spin coating procedure was given recently... [Pg.53]

The synthetic polymer Nation is an anionic, inert polymer that has hydrophilic and hydrophobic properties. Nation is composed of perfluorosulfonic acid and has shown to increase the lifetime of sensors and to decrease the inflammatory response in the short term and decrease interferents (believed to be due to the anionic property). Nation can be applied as an outer coating to sensors through a dip coating or spin coating procedure to entrap the enzyme and improve biocompatibility of the... [Pg.229]

Using preformed redox polymers as electrode modifiers has the advantage of completely characterizing polymers prior to modifying the electrode surface. Control of the layer thickness of the deposited films can be achieved by carefully controlling the amount deposited by using drop- or spin-coating procedures. [Pg.270]

Spin coating is a useful method for laying down onto an infrared transparent window a uniform thin layer of a few micrometers thickness of a polymer from a solution. A film can conveniently be cast from a polymer that is soluble in a convenient solvent at a concentration of 1-2%. An example of a spin-coater is shown in Figure 4 a clean 13 mm diameter window is attached to the sample stub, onto which several drops of the solution are laid down from a pipette, after which the rotor is spim for a few seconds. Thin films on gold-coated disks suitable for reflection-absorption measurements (see the section Thin films on metallic substrates ), may also be prepared by the spin-coating procedure. [Pg.2236]

These data show that the modelling of the spin coating procedure gives a reasonable estimate of the amount of deposited material. [Pg.1168]

The authors thank Ing. P. van Acker and E. Rodenburg for their help with the spin-coating procedure. We also thank Dr.A. Knoester and Ing. N. Groesbeek from the Royal/Dutch Shell Laboratory in Amsterdam for the HRSEM measurements. Dr. H. Zandbergen is acknowledged for the TEM measurements. [Pg.1170]

ICD always presents a major Cotton band at 200nm and a minor Cotton band of opposite sign at 223 nm, but its intensity is critically dependent on the him processing. In particular, maximum ICD intensities (in the presence of all the considered non-racemic molecules) have been observed for SPS hlms spin-coated from chloroform solutions, for spin rates larger than 1600 rpm (Fig. 10.12). The ICD phenomena are instead negligible for spin-coating procedures with most solvents and always for spin rates lower than 100 rpm [192]. [Pg.223]

Fig. 10. Formation of noncentrosymmetric multilayer film by combining self-assembly and a surface S 2 reaction, where R = (CH2)30H procedure I = spin-coating followed by annealing at 110°C and procedure II = reaction of Cl2Si0SiCl20SiCl2, ie, a dilute solution of 4-[A/,A/,-bis-(3-hydroxyprop5l)-aminophenylazo]-4 -pyridine on a benzyl chloride SAM surface was used, resulting in facile formation of SAMs having high... Fig. 10. Formation of noncentrosymmetric multilayer film by combining self-assembly and a surface S 2 reaction, where R = (CH2)30H procedure I = spin-coating followed by annealing at 110°C and procedure II = reaction of Cl2Si0SiCl20SiCl2, ie, a dilute solution of 4-[A/,A/,-bis-(3-hydroxyprop5l)-aminophenylazo]-4 -pyridine on a benzyl chloride SAM surface was used, resulting in facile formation of SAMs having high...
Figure 5. Sorbic acid molecules on HOPG as reported by Smith et. al. (10). This surface was prepared by spin-coating a dilute sorbic acid-benzene solution onto a freshly cleaved HOPG substrate. Images of the surface were obtained in liquid helium. The elongated structure shown was representative of those present on surfaces prepared with this procedure. Figure 5. Sorbic acid molecules on HOPG as reported by Smith et. al. (10). This surface was prepared by spin-coating a dilute sorbic acid-benzene solution onto a freshly cleaved HOPG substrate. Images of the surface were obtained in liquid helium. The elongated structure shown was representative of those present on surfaces prepared with this procedure.
Sample Preparation. PBS-MP20, obtained in powder form from Mead Chemical Co., was the primary source of the samples used in this study. A portion of the MP20 powder was dissolved in 2-methoxyethyl acetate (Mead Chemical) and films were spin-coated on silicon wafers. Films were baked at 120 C for 1 hour prior to irradiation. MP20 samples, both in powder and film form, were irradiated under vacuum at 30 C in a Co source. Films were spun from methoxyethyl acetate solutions of the irradiated powders. These films were also baked at 120 C for 1 hour. The above procedure created two types of degraded MP20 samples (1) those irradiated in film form and (2) those irradiated in powder form. The first type of films were designated as IF-type films. Films spun from solutions of the irradiated powders were designated as IP-type films. [Pg.21]

Another important aspect is the proximity of particle layer and thin or thick films, whereby the border between thin and thick films remains ambiguous. Conventional processing of particle assemblies comprises molding of the particle mass, like dry compression or wet casting. In the case of nanoparticles, to form a film is much more rational than conventional powder processing. In a dry procedure, production of nanoparticles and film formation in most cases take place simultaneously. An assembly of nanoparticles can also be formed in a wet procedure by precipitation on the templates or even by simple dip or spin coating from a sol containing nanoparticles. [Pg.683]

Formulation of Resist Solutions. Forty grams of a Novolak resin was mixed with 10 g of the photoactive compound, and dissolved in 100 g of bis-2-methoxy-ethylether. After wafers were spin-coated, the samples were immediately placed on a hot plate at 82 C for 14 min. The formulation procedure of a composite resist of poly (2-methyl-1-pentene sulfone) in the Novolak resin is as follows the polysulfone was mixed with the resin (13 wt% solid), and then dissolved in 2-methoxyethyl acetate the films were spin-coated onto silicon wafers, and then baked at 100°C for 20 min prior to electron beam exposure. [Pg.345]

In one recent study, Mn2+-doped CdS nanocrystals grown with a ZnS passivating shell were used as the recombination centers in direct current (dc) electroluminescent devices (104). The Mn2+ CdS/ZnS nanocrystals were prepared by the inverse micelle procedure (102) (see Section II.C) and these colloids were incorporated into a multilayer device structure by spin-coat... [Pg.110]

In Chapter 10, the use of membranes for different applications are described. One of the possible membranes for hydrogen cleaning is an asymmetric membrane comprised of the dense end of a proton conduction perovskite such as BaCe0 95 Yb0 05O3 5 and a porous end to bring mechanical stability to the membrane. In this case, it is possible to take from the slurry, obtained by the acetate procedure, several drops to be released over a porous ceramic membrane, located in the spinning bar of a spin-coating machine. Thereafter, the assembly powder, thin film porous membrane is heated from room temperature up to 1573 K at a rate of 2K/min, kept at this temperature for 12 h, and then cooled at the same rate in order to get the perovskite end film over the porous membrane [50],... [Pg.115]


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See also in sourсe #XX -- [ Pg.223 ]




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Coatings spin-coated

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