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Dispersion sheets

Obstacles to greater nanofiller use remain, and just explaining these challenges requires a new set of terminology. The main issue is that nanofiller partides are difficult to disperse meaning that actual nanocomposite properties may not reach their potential or theoretical properties. For example, for proper dispersal, sheet-like nanoday platelets must be exfoliated, physically or chemically, to separate them into individual layers. This issue is probably the most discussed and most problematic obstade impeding the full commerdal-ization of nanocomposite compounds, since the full surface area of each separated sheet or platdet is what creates optimum properties [7-31, 7-32[. [Pg.110]

Simulsol 78 Simulsol 98 Simulsol CS dispersant, sheeted baked snacks CHiForm 12791 dispersant, shellac Triethanolamine dispersant, shoe polishes Dig lycol/CHDM/lsophthalates/SIP copolymer Eastman AQ 29D Eastman AQ 35S Eastman AQ38D Eastman AQ 38S Eastman AQ55S dispersant, shortening Glycosperse O-20 KFG Solec 3F SB dispersant, shower baths Texapon SPN 70 dispersant, shower gels Mapeg 6000 DS... [Pg.2636]

A major advance in force measurement was the development by Tabor, Win-terton and Israelachvili of a surface force apparatus (SFA) involving crossed cylinders coated with molecularly smooth cleaved mica sheets [11, 28]. A current version of an apparatus is shown in Fig. VI-4 from Ref. 29. The separation between surfaces is measured interferometrically to a precision of 0.1 nm the surfaces are driven together with piezoelectric transducers. The combination of a stiff double-cantilever spring with one of a number of measuring leaf springs provides force resolution down to 10 dyn (10 N). Since its development, several groups have used the SFA to measure the retarded and unretarded dispersion forces, electrostatic repulsions in a variety of electrolytes, structural and solvation forces (see below), and numerous studies of polymeric and biological systems. [Pg.236]

Circular dicliroism has been a useful servant to tire biophysical chemist since it allows tire non-invasive detennination of secondary stmcture (a-helices and P-sheets) in dissolved biopolymers. Due to tire dissymmetry of tliese stmctures (containing chiral centres) tliey are biaxial and show circular birefringence. Circular dicliroism is tlie Kramers-Kronig transfonnation of tlie resulting optical rotatory dispersion. The spectral window useful for distinguishing between a-helices and so on lies in tlie region 200-250 nm and hence is masked by certain salts. The metliod as usually applied is only semi-quantitative, since tlie measured optical rotations also depend on tlie exact amino acid sequence. [Pg.2819]

Steeping. Sheet, roU, or suitably milled flock pulp is metered into a pulper along with vigorously stirred 18% sodium hydroxide solution at 50°C. The resulting slurry, containing about 5% finely dispersed pulp, passes to a buffer tank from which it is metered to a slurry press that sieves out the swollen fiber and returns the pressings soda for concentration correction and reuse. The cellulose reacts with the soda as a complex alcohol to form the sodium salt or alk-ceU. [Pg.346]

Fig. 16. Two-hquid flotation flow sheet (39). The original ROM is kaolin (white clay) that contains 11% impurity in the form of mica, anatase, and siUca. Treatment produces high purity kaolin and a Ti02-rich fraction. A, Kaolin stockpile D, dispersant (sodium siUcate plus alkah) W, water K, kerosene C, collector (sodium oleate) RK, recycled kerosene S, screen M, inline mixer SPR, separator CFG, centrifuge P, product and T, to waste. Fig. 16. Two-hquid flotation flow sheet (39). The original ROM is kaolin (white clay) that contains 11% impurity in the form of mica, anatase, and siUca. Treatment produces high purity kaolin and a Ti02-rich fraction. A, Kaolin stockpile D, dispersant (sodium siUcate plus alkah) W, water K, kerosene C, collector (sodium oleate) RK, recycled kerosene S, screen M, inline mixer SPR, separator CFG, centrifuge P, product and T, to waste.
Fiber-reiaforced panels covered with PVF have been used for greenhouses. Transparent PVF film is used as the cover for flat-plate solar collectors (114) and photovoltaic cells (qv) (115). White PVF pigmented film is used as the bottom surface of photovoltaic cells. Nonadhering film is used as a release sheet ia plastics processiag, particularly ia high temperature pressing of epoxy resias for circuit boards (116—118) and aerospace parts. Dispersions of PVF are coated on the exterior of steel hydrauHc brake tubes and fuel lines for corrosion protection. [Pg.382]

As a general rule, however, textile fibers do not wet out readily, are difficult to disperse, and tend to tangle with one another. Consequendy, large amounts of water are necessary to keep the fibers suspended. Further, if the slurry is not handled propedy, the fibers tangle and cause poor sheet formation. Two approaches to resolving these difficulties are increasing slurry—dilution ratio and controlling fiber orientation. [Pg.152]

Papermaking additives can be categorized either as process additives or as functional additives. Process additives are materials that improve the operation of the paper machine, such as retention and drainage aids, biocides, dispersants, and defoamers they are primarily added at the wet end of the paper machine. Functional additives are materials that enhance or alter specific properties of the paper product, such as fillers (qv), sizing agents, dyes, optical brighteners, and wet- and dry-strength additives they may be added internally or to the surface of the sheet. [Pg.15]

The most widely used pitch control method is the addition of pitch dispersants, which can be either organic, ie, typically anionic polymers such as naphthalene sulfonates, ligninsulfonates, and polyacrylates (33,34), or inorganic, ie, typically clay or talc. The polymers maintain the pitch as a fine dispersion in the pulp, preventing agglomeration and potential deposition on the paper machine or the sheet. When talc, clay, or other adsorbent fillers are added to the furnish, moderate amounts of pitch can adsorb on these materials, producing a nontacky soHd that can be retained in the sheet. [Pg.16]

Color intensity and permanence are improved by metal carboxylate salts, especially 2inc salts (83), which cataly2e the dye development and stabili2e the dye in its colored form. The substituted novolak resin, along with extender and binder, can be apphed to the receiving sheet as a solution or aqueous dispersion. Aqueous dispersions are probably the most widely used they are manufactured by the resin suppher or the user from the base resin. [Pg.304]

The first satisfactory photographic film was produced in 1888 when gelatin-dispersed microcrystals of silver haUde were coated on celluloid sheets (23). Within a year George Eastman prepared and marketed toU films on a base produced by dissolving nitrocellulose with camphor and amyl acetate in methanol (qv). [Pg.440]

The processing methods for siHcone mbber are similar to those used in the natural mbber industry (59,369—371). Polymer gum stock and fillers are compounded in a dough or Banbury-type mixer. Catalysts are added and additional compounding is completed on water-cooled roU mills. For small batches, the entire process can be carried out on a two-roU mill. Heat-cured siHcone mbber is commercially available as gum stock, reinforced gum, partially filled gum, uncatalyzed compounds, dispersions, and catalyzed compounds. The latter is ready for use without additional processing. Before being used, sihcone mbber is often freshened, ie, the compound is freshly worked on a mbber mill until it is a smooth continuous sheet. The freshening process eliminates the stmcturing problems associated with polymer—filler interactions. [Pg.53]

Demonstrations (a) Atomix (to show grain boundaries), (b) Model of dispersion strengthening. Take piece of PMMA sheet == 2.5 mm thick and = 7 cm square. Glue four PMMA strips of section =7X7 mm on top of the sheet to form a tray = 7 mm deep. Cut six = 7-mm lengths of an = 6-mm-diameter PMMA rod. Glue the ends of these to... [Pg.291]

Closely related to the ID dispersion relations for the carbon nanotubes is the ID density of states shown in Fig. 20 for (a) a semiconducting (10,0) zigzag carbon nanotube, and (b) a metallic (9,0) zigzag carbon nanotube. The results show that the metallic nanotubes have a small, but non-vanishing 1D density of states, whereas for a 2D graphene sheet (dashed curve) the density of states... [Pg.71]


See other pages where Dispersion sheets is mentioned: [Pg.274]    [Pg.225]    [Pg.274]    [Pg.225]    [Pg.180]    [Pg.65]    [Pg.1145]    [Pg.18]    [Pg.312]    [Pg.313]    [Pg.24]    [Pg.267]    [Pg.295]    [Pg.370]    [Pg.374]    [Pg.378]    [Pg.400]    [Pg.122]    [Pg.247]    [Pg.71]    [Pg.252]    [Pg.7]    [Pg.3]    [Pg.16]    [Pg.22]    [Pg.178]    [Pg.230]    [Pg.8]    [Pg.122]    [Pg.440]    [Pg.335]    [Pg.458]    [Pg.228]    [Pg.366]    [Pg.39]    [Pg.244]    [Pg.76]    [Pg.335]   
See also in sourсe #XX -- [ Pg.274 ]




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