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Phases and Coatings

Pyrolyses of siloxane materials leads to ceramic-like phases. For example, ceramic fibers based on silicon carbide have been prepared from polycar-bosilane/polymethylphenylsiloxane polymer blends.  [Pg.45]

PDMS coatings have been made less oleophobic by modifying them using copolyacrylate side chains some of which are semifiuorinated or PDMS itself. Also relevant here are UV-curable bismaleimides containing PDMS as hydrophobic agents.  [Pg.45]

PDMS emerged as the polymer of choice for micropatterned surfaces and microfluidic devices. Fabrication is particularly straightforward since PDMS can be cast against a suitable mold with high fidelity. The optical, thermal, interfacial, permeability, and reactivity properties of PDMS make possible numerous functionalities including optical detection, reversible deformation, reversible wetting, and management of cell proliferation.  [Pg.45]


The complex mixtures of methylated alditol acetates, often obtained after methylation analysis, cannot be adequately resolved on conventional packed GLC columns. The fractionation of large numbers of these derivatives now can be achieved using capillary columns (Geyer et al., 1982). It is unlikely that a single column can adequately resolve all the derivatives from the methylation analysis of plant cell walls (Lomax et al., 1985). A combination of different liquid phases and coating procedures, namely wall-coated (WCOT), support-coated (SCOT), and permanently bonded (BP) phases will be required (Geyer et al., 1982 Lomax et al., 1985). As an alternative to PMAA, partially ethylated alditol acetates may be used... [Pg.93]

Analytical separations may be classified in three ways by the physical state of the mobile phase and stationary phase by the method of contact between the mobile phase and stationary phase or by the chemical or physical mechanism responsible for separating the sample s constituents. The mobile phase is usually a liquid or a gas, and the stationary phase, when present, is a solid or a liquid film coated on a solid surface. Chromatographic techniques are often named by listing the type of mobile phase, followed by the type of stationary phase. Thus, in gas-liquid chromatography the mobile phase is a gas and the stationary phase is a liquid. If only one phase is indicated, as in gas chromatography, it is assumed to be the mobile phase. [Pg.546]

Capillary Electrochromatography Another approach to separating neutral species is capillary electrochromatography (CEC). In this technique the capillary tubing is packed with 1.5-3-pm silica particles coated with a bonded, nonpolar stationary phase. Neutral species separate based on their ability to partition between the stationary phase and the buffer solution (which, due to electroosmotic flow, is the mobile phase). Separations are similar to the analogous HPLC separation, but without the need for high-pressure pumps, furthermore, efficiency in CEC is better than in HPLC, with shorter analysis times. [Pg.607]

Zhou and colleagues determined the %w/w H2O in methanol by GG, using a capillary column coated with a nonpolar stationary phase and a thermal conductivity detector. A series of calibration standards gave the following results. [Pg.616]

In general, the longer a chromatographic column, the better will be the separation of mixture components. In modem gas chromatography, columns are usually made from quartz and tend to be very long (coiled), often 10-50 m, and narrow (0.1-1.0 mm, internal diameter) — hence their common name of capillary columns. The stationary phase is coated very thinly on the whole length of the inside wall of the capillary column. Typically, the mobile gas phase flows over the stationary phase in the column at a rate of about 1-2 ml/min. [Pg.249]

Classification of the many different encapsulation processes is usehil. Previous schemes employing the categories chemical or physical are unsatisfactory because many so-called chemical processes involve exclusively physical phenomena, whereas so-called physical processes can utilize chemical phenomena. An alternative approach is to classify all encapsulation processes as either Type A or Type B processes. Type A processes are defined as those in which capsule formation occurs entirely in a Hquid-filled stirred tank or tubular reactor. Emulsion and dispersion stabiUty play a key role in determining the success of such processes. Type B processes are processes in which capsule formation occurs because a coating is sprayed or deposited in some manner onto the surface of a Hquid or soHd core material dispersed in a gas phase or vacuum. This category also includes processes in which Hquid droplets containing core material are sprayed into a gas phase and subsequentiy solidified to produce microcapsules. Emulsion and dispersion stabilization can play a key role in the success of Type B processes also. [Pg.318]

Suspension Polymerization. At very low levels of stabilizer, eg, 0.1 wt %, the polymer does not form a creamy dispersion that stays indefinitely suspended in the aqueous phase but forms small beads that setde and may be easily separated by filtration (qv) (69). This suspension or pearl polymerization process has been used to prepare polymers for adhesive and coating appHcations and for conversion to poly(vinyl alcohol). Products in bead form are available from several commercial suppHers of PVAc resins. Suspension polymerizations are carried out with monomer-soluble initiators predominantly, with low levels of stabilizers. Suspension copolymerization processes for the production of vinyl acetate—ethylene bead products have been described and the properties of the copolymers determined (70). Continuous tubular polymerization of vinyl acetate in suspension (71,72) yields stable dispersions of beads with narrow particle size distributions at high yields. [Pg.465]

Preferential deposition of weaMy adsorbed dissolved components on the outer surface of the catalyst body is a similar phenomenon but can occur after impregnation during removal of the solvent. When the impregnated particle is heated, the Hquid phase expands and coats the exterior surfaces with dissolved species as the solvent evaporates. In particularly severe cases, the entire outer surface of the catalyst can become completely coated with a soHd that blocks access to the underlying pore stmcture. [Pg.196]

Viscosity of Systems with Dispersed Phases. A large proportion of coatings are pigmented and, therefore, have dispersed phases. In latex paints, both the pigments and the principal polymer are in dispersed phases. The viscosity of a coating having dispersed phases is a function of the volume concentration of the dispersed phase and can be expressed mathematically by the Mooney equation (96), a convenient form of which is... [Pg.346]

What of the corrosion resistance of new turbine-blade alloys like DS eutectics Well, an alloy like NiaAl-NisNb loses 0.05 mm of metal from its surface in 48 hours at the anticipated operating temperature of 1155°C for such alloys. This is obviously not a good performance, and coatings will be required before these materials are suitable for application. At lower oxidation rates, a more insidious effect takes place - preferential attack of one of the phases, with penetration along interphase boundaries. Obviously this type of attack, occurring under a break in the coating, can easily lead to fatigue failure and raises another problem in the use of DS eutectics. [Pg.223]

Lead is an element used in many industrial processes and also has been used in fuels and coatings. Tetraethyl lead was added to gasoline to improve performance as a motor fuel, and elemental lead was extensively used in paints and coatings to improve coverage and durability until the 1970s, when phase-out efforts began to reduce lead emissions to the environment. [Pg.50]


See other pages where Phases and Coatings is mentioned: [Pg.168]    [Pg.582]    [Pg.45]    [Pg.131]    [Pg.582]    [Pg.242]    [Pg.168]    [Pg.582]    [Pg.45]    [Pg.131]    [Pg.582]    [Pg.242]    [Pg.361]    [Pg.546]    [Pg.547]    [Pg.564]    [Pg.66]    [Pg.320]    [Pg.320]    [Pg.322]    [Pg.129]    [Pg.129]    [Pg.136]    [Pg.54]    [Pg.130]    [Pg.270]    [Pg.481]    [Pg.279]    [Pg.209]    [Pg.209]    [Pg.445]    [Pg.106]    [Pg.35]    [Pg.2124]    [Pg.184]    [Pg.107]    [Pg.445]    [Pg.453]    [Pg.429]    [Pg.443]    [Pg.529]    [Pg.633]    [Pg.4]    [Pg.313]   


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