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Vinyl alcohol, and

Currently, almost all acetic acid produced commercially comes from acetaldehyde oxidation, methanol or methyl acetate carbonylation, or light hydrocarbon Hquid-phase oxidation. Comparatively small amounts are generated by butane Hquid-phase oxidation, direct ethanol oxidation, and synthesis gas. Large amounts of acetic acid are recycled industrially in the production of cellulose acetate, poly(vinyl alcohol), and aspirin and in a broad array of other... [Pg.66]

The web materials used to form dmms and cans can be customized to each packaging apphcation. The materials are selected based on the package properties of moisture and humidity resistance, nonstick resistance, or barrier properties required. The adhesives used to bond the phes together include sihcates, poly(vinyl alcohol), and poly(vinyl acetate) (10). Sihcate adhesives are most commonly used in the manufacture of dmm packages. [Pg.519]

Functional derivatives of polyethylene, particularly poly(vinyl alcohol) and poly(acryLic acid) and derivatives, have received attention because of their water-solubility and disposal iato the aqueous environment. Poly(vinyl alcohol) is used ia a wide variety of appHcations, including textiles, paper, plastic films, etc, and poly(acryLic acid) is widely used ia detergents as a builder, a super-absorbent for diapers and feminine hygiene products, for water treatment, ia thickeners, as pigment dispersant, etc (see Vinyl polymers, vinyl alcohol polymers). [Pg.479]

Other typical pyrotechnic fuels include charcoal, sulfur, boron, siUcon, and synthetic polymers such as poly(vinyl alcohol) and poly(vinyl chloride). Extensive use has been made of natural products such as starches and gums, and the use of these materials continues to be substantial in the fireworks industry. MiUtary pyrotechnics have moved away from the use of natural products due to the inherent variabiUty in these materials depending on climatic conditions during the growth of the plants from which the compounds are derived. [Pg.347]

The thermal glass-transition temperatures of poly(vinyl acetal)s can be determined by dynamic mechanical analysis, differential scanning calorimetry, and nmr techniques (31). The thermal glass-transition temperature of poly(vinyl acetal) resins prepared from aliphatic aldehydes can be estimated from empirical relationships such as equation 1 where OH and OAc are the weight percent of vinyl alcohol and vinyl acetate units and C is the number of carbons in the chain derived from the aldehyde. The symbols with subscripts are the corresponding values for a standard (s) resin with known parameters (32). The formula accurately predicts that resin T increases as vinyl alcohol content increases, and decreases as vinyl acetate content and aldehyde carbon chain length increases. [Pg.450]

Poly(vinyl acetate) emulsions can be made with a surfactant alone or with a protective coUoid alone, but the usual practice is to use a combination of the two. Normally, up to 3 wt % stabilizers may be included in the recipe, but when water sensitivity or tack of the wet film is desired, as in some adhesives, more may be included. The most commonly used surfactants are the anionic sulfates and sulfonates, but cationic emulsifiers and nonionics are also suitable. Indeed, some emulsion compounding formulas require the use of cationic or nonionic surfactants for stable formulations. The most commonly used protective coUoids are poly(vinyl alcohol) and hydroxyethyl cellulose, but there are many others, natural and synthetic, which are usable if not preferable for a given appHcation. [Pg.464]

Poly(vinyl alcohol) [9002-89-5] was discovered through the addition of alkaU to a clear alcohoHc solution of poly(vinyl acetate), which resulted in the ivory-colored poly(vinyl alcohol) (4). The same discovery has been made by studying the reversible transformation between poly(vinyl alcohol) and poly(vinyl acetate) via esterification and saponification (5). The first scientific reports on poly(vinyl alcohol) were pubUshed in 1927 (6,7). [Pg.475]

Poly(vinyl nitrate) has been prepared and studied for use in explosives and rocket fuel (104,105). Poly(vinyl alcohol) and sulfur trioxide react to produce poly(vinyl sulfate) (106—111). Poly(vinyl alkane sulfonate)s have been prepared from poly(vinyl alcohol) and alkanesulfonyl chlorides (112—114). In the presence of urea, poly(vinyl alcohol) and phosphoms pentoxide (115) or phosphoric acid (116,117) yield poly(vinyl phosphate)s. [Pg.481]

Reaction between poly(vinyl alcohol) and isocyanates yields substituted carbamate esters (127—134) ... [Pg.481]

Acetalization. Poly(vinyl alcohol) and aldehydes form compounds of industrial mi o t2in.ceJntramoiecuiaracetaii tion... [Pg.481]

PuUy hydroly2ed poly(vinyl alcohol) and iodine form a complex that exhibits a characteristic blue color similar to that formed by iodine and starch (171—173). The color of the complex can be enhanced by the addition of boric acid to the solution consisting of iodine and potassium iodide. This affords a good calorimetric method for the deterrnination of poly(vinyl alcohol). Color intensity of the complex is effected by molecular weight, degree of... [Pg.481]

Because of the many choices of hydrophilic monomers, cross-linkers, and hydrophobic monomers, a large number of formulations have been developed and manufactured into hydrogel lenses. The water content of these hydrogel lenses ranges from about 38%, for HEMA-based lenses, to 80%, for poly(vinyl alcohol) and partially hydrolysed acrylonitrile lenses. Table 2 gives a representative Hst of FDA approved hydrogel materials available to the consumer in the early 1990s. [Pg.104]

Because of its high cold flow, poly(vinyl acetate) is of little value in the form of mouldings and extrusions. However, because of its good adhesion to a number of substrates, and to some extent because of its cold flow, a large quantity is produced for use in emulsion paints, adhesives and various textile finishing operations. A minor proportion of the material is also converted into poly(vinyl alcohol) and the poly(vinyl acetal)s which, are of some interest to the plastics industry. [Pg.386]

Since poly(vinyl acetate) is usually used in an emulsion form, the emulsion polymerisation process is commonly used. In a typical system, approximately equal quantities of vinyl acetate and water are stirred together in the presence of a suitable colloid-emulsifier system, such as poly(vinyl alcohol) and sodium lauryl sulphate, and a water-soluble initiator such as potassium persulphate. [Pg.388]

The C-C-R bond angle changes significantly in the 0° conformation of vinyl alcohol and in vinyl amine. In all of these vinyl systems, the substituent shortens the C-H bond (on the carbon to which the substituent is attached), most dramatically in the case of the substituents NHj and OH. [Pg.52]

If you completed the previous exercises in this chapter, you ve already run the jobs for vinyl alcohol and vinyl amine. [Pg.80]

On saponification this last compound yields vinyl alcohol and phenyl-acetaldehyde and alcohol, thus —... [Pg.195]

Thermally reversible gels can be prepared from poly (vinyl alcohol) and alkali metal salts of o-hydroxybenzal derivatives having benzenoid groups at both ends 24). Colored gels can be obtained, depending on the type of ketone used (Figure 4). [Pg.15]

A dispersant that can be used in drilling fluids, spacer fluids, cement slurries, completion fluids, and mixtures of drilling fluids and cement slurries controls the rheologic properties of and enhances the filtrate control in these fluids. The dispersant consists of polymers derived from monomeric residues, including low-molecular-weight olefins that may be sulfonated or phosphonated, unsaturated dicarboxylic acids, ethylenically unsaturated anhydrides, unsaturated aliphatic monocarboxylic acids, vinyl alcohols and diols, and sulfonated or phosphonated styrene. The sulfonic acid, phosphonic acid, and carboxylic acid groups on the polymers may be present in neutralized form as alkali metal or ammonium salts [192,193]. [Pg.311]

NA Peppas. Hydrogels of poly(vinyl alcohol) and its copolymers. In NA Peppas, ed. Hydrogels in Medicine and Pharmacy, Vol. II Polymers. Boca Raton, FL CRC... [Pg.546]

Vijay Kumar R, Elgamiel R, Diamant Y, Gedanken A (2001) Sonochemical preparation and characterization of nanocrystalline copper oxide embedded in poly(vinyl alcohol) and Its effect on crystal growth of copper oxide. Langmuir 17(5) 1406-1410... [Pg.266]

The identification of anionic polyfacrylic acid) sizes can be carried out by staining with a fluorescent cationic dye (Cl Basic Orange 14) followed by spectroscopic measurement of excitation wavelength and fluorescence emission [195,196]. Such methods can also be used (with Cl Basic Orange 14 or Cl Basic Red 1) to detect and estimate carboxymethylcellulose, poly(vinyl alcohol) and starch derivatives [197]. [Pg.109]

The basis of ultrafiltration is that a liquor is passed through a membrane many times until the required concentration of the permeate is attained. Fouling of the membrane can be a problem and regular cleaning and disinfection of the membrane is recommended. Ultrafiltration of poly(vinyl alcohol) and starch sizes offers economic advantages over... [Pg.110]


See other pages where Vinyl alcohol, and is mentioned: [Pg.22]    [Pg.194]    [Pg.284]    [Pg.337]    [Pg.68]    [Pg.42]    [Pg.298]    [Pg.472]    [Pg.479]    [Pg.229]    [Pg.164]    [Pg.449]    [Pg.463]    [Pg.466]    [Pg.471]    [Pg.498]    [Pg.152]    [Pg.54]    [Pg.404]    [Pg.10]    [Pg.168]    [Pg.11]    [Pg.87]    [Pg.429]    [Pg.479]    [Pg.486]    [Pg.109]    [Pg.111]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.2 , Pg.328 ]




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