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Vinyl starch

If the substituents are not stable during acid hydrolysis or methanolysis, the complementary substitution pattern can be determined after permethylation, as already noted. Examples are organic (acetates) and inorganic esters (sulfates), and benzyl and silyl ethers. " Such an approach was applied as early as 1964 to vinyl starches."" In contrast to the direct determination of the substituent pattern, incomplete methylation and consequently erroneous evaluations cannot be recognized from the product pattern obtained in the indirect methods. If the average DS is known from an independent determination, it allows at least a certain control. Therefore, the absence of OH absorption should be carefully monitored by IR spectroscopy. [Pg.157]

Dichromated Resists. The first compositions widely used as photoresists combine a photosensitive dichromate salt (usually ammonium dichromate) with a water-soluble polymer of biologic origin such as gelatin, egg albumin (proteins), or gum arabic (a starch). Later, synthetic polymers such as poly(vinyl alcohol) also were used (11,12). Irradiation with uv light (X in the range of 360—380 nm using, for example, a carbon arc lamp) leads to photoinitiated oxidation of the polymer and reduction of dichromate to Ct(III). The photoinduced chemistry renders exposed areas insoluble in aqueous developing solutions. The photochemical mechanism of dichromate sensitization of PVA (summarized in Fig. 3) has been studied in detail (13). [Pg.115]

Many of these reactions are reversible, and for the stronger nucleophiles they usually proceed the fastest. Typical examples are the addition of ammonia, amines, phosphines, and bisulfite. Alkaline conditions permit the addition of mercaptans, sulfides, ketones, nitroalkanes, and alcohols to acrylamide. Good examples of alcohol reactions are those involving polymeric alcohols such as poly(vinyl alcohol), cellulose, and starch. The alkaline conditions employed with these reactions result in partial hydrolysis of the amide, yielding mixed carbamojdethyl and carboxyethyl products. [Pg.133]

Suitable protective coUoids for the preparation of acryhc suspension polymers include ceUulose derivatives, polyacrylate salts, starch, poly(vinyl alcohol), gelatin, talc, clay, and clay derivatives (95). These materials are added to prevent the monomer droplets from coalescing during polymerisation (110). Thickeners such as glycerol, glycols, polyglycols, and inorganic salts ate also often added to improve the quahty of acryhc suspension polymers (95). [Pg.169]

Water-Soluble Films. Water-soluble films can be produced from such polymers as poly(vinyl alcohol) (PVOH), methylceUulose, poly(ethylene oxide), or starch (qv) (see Cellulose ethers Polyethers Vinyl polymers). Water-soluble films are used for packaging and dispensing portions of detergents, bleaches, and dyes. A principal market is disposable laundry bags for hospital use. Disposal packaging for herbicides and insecticides is an emerging use. [Pg.378]

Attempts have been made to use cold-set adhesives in the cormgating operation, such as poly(vinyl acetate) and modified, precooked starch formulations, but these have not achieved any appreciable degree of commercial acceptance (20). The use of a polyethylene film appHed to the inside surface of the linerboard facing, which serves as a hot-melt cormgator adhesive, has achieved some commercial usage. However, its use is limited to the small, specialty product niche of fast-food hamburger cartons (see Olefin polymers, polyethylene). [Pg.518]

The paster is a nonheated operation. The most common paster adhesive formulation consists of poly(vinyl alcohol)—clay—starch blends (10). A 100% area adhesive coverage is used. The rate of bond strength development of the adhesive is an important commercial concern and rapid bond formation rates are desirable. [Pg.519]

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]

Pyrotechnic mixtures may also contain additional components that are added to modify the bum rate, enhance the pyrotechnic effect, or serve as a binder to maintain the homogeneity of the blended mixture and provide mechanical strength when the composition is pressed or consoHdated into a tube or other container. These additional components may also function as oxidizers or fuels in the composition, and it can be anticipated that the heat output, bum rate, and ignition sensitivity may all be affected by the addition of another component to a pyrotechnic composition. An example of an additional component is the use of a catalyst, such as iron oxide, to enhance the decomposition rate of ammonium perchlorate. Diatomaceous earth or coarse sawdust may be used to slow up the bum rate of a composition, or magnesium carbonate (an acid neutralizer) may be added to help stabilize mixtures that contain an acid-sensitive component such as potassium chlorate. Binders include such materials as dextrin (partially hydrolyzed starch), various gums, and assorted polymers such as poly(vinyl alcohol), epoxies, and polyesters. Polybutadiene mbber binders are widely used as fuels and binders in the soHd propellant industry. The production of colored flames is enhanced by the presence of chlorine atoms in the pyrotechnic flame, so chlorine donors such as poly(vinyl chloride) or chlorinated mbber are often added to color-producing compositions, where they also serve as fuels. [Pg.347]

Etherification and esterification of hydroxyl groups produce derivatives, some of which are produced commercially. Derivatives may also be obtained by graft polymerization wherein free radicals, initiated on the starch backbone by ceric ion or irradiation, react with monomers such as vinyl or acrylyl derivatives. A number of such copolymers have been prepared and evaluated in extmsion processing (49). A starch—acrylonitrile graft copolymer has been patented (50) which rapidly absorbs many hundred times its weight in water and has potential appHcations in disposable diapers and medical suppHes. [Pg.342]

Low DS starch acetates ate manufactured by treatment of native starch with acetic acid or acetic anhydride, either alone or in pyridine or aqueous alkaline solution. Dimethyl sulfoxide may be used as a cosolvent with acetic anhydride to make low DS starch acetates ketene or vinyl acetate have also been employed. Commercially, acetic anhydride-aqueous alkaU is employed at pH 7—11 and room temperature to give a DS of 0.5. High DS starch acetates ate prepared by the methods previously detailed for low DS acetates, but with longer reaction time. [Pg.345]

Polymers. In combination with various metal salts, sorbitol is used as a stabilizer against heat and light in poly(vinyl chloride) (qv) resins and, with a phenohc antioxidant, as a stabilizer in uncured styrene—butadiene mbber (qv) compositions and in polyolefins (see Heat stabilizers Olefin POLYMERS Rubbercompounding). Heat-sealable films are prepared from a dispersion of sorbitol and starch in water (255). Incorporation of sorbitol in coUagen films gready restricts their permeabiUty to carbon dioxide (256). [Pg.55]

Although they lack commercial importance, many other poly(vinyl acetal)s have been synthesized. These include acetals made from vinyl acetate copolymerized with ethylene (43—46), propjiene (47), isobutjiene (47), acrylonitrile (48), acrolein (49), acrylates (50,47), aHyl ether (51), divinyl ether (52), maleates (53,54), vinyl chloride (55), diaHyl phthalate (56), and starch (graft copolymer) (47). [Pg.450]

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]

Some commercial durable antistatic finishes have been Hsted in Table 3 (98). Early patents suggest that amino resins (qv) can impart both antisHp and antistatic properties to nylon, acryUc, and polyester fabrics. CycHc polyurethanes, water-soluble amine salts cross-linked with styrene, and water-soluble amine salts of sulfonated polystyrene have been claimed to confer durable antistatic protection. Later patents included dibydroxyethyl sulfone [2580-77-0] hydroxyalkylated cellulose or starch, poly(vinyl alcohol) [9002-86-2] cross-linked with dimethylolethylene urea, chlorotria2ine derivatives, and epoxy-based products. Other patents claim the use of various acryUc polymers and copolymers. Essentially, durable antistats are polyelectrolytes, and the majority of usehil products involve variations of cross-linked polyamines containing polyethoxy segments (92,99—101). [Pg.294]

Poly(vinyl acetate) is too soft and shows excessive cold flow for use in moulded plastics. This is no doubt associated with the fact that the glass transition temperature of 28°C is little above the usual ambient temperatures and in fact in many places at various times the glass temperature may be the lower. It has a density of 1.19 g/cm and a refractive index of 1.47. Commercial polymers are atactic and, since they do not crystallise, transparent (if free from emulsifier). They are successfully used in emulsion paints, as adhesives for textiles, paper and wood, as a sizing material and as a permanent starch . A number of grades are supplied by manufacturers which differ in molecular weight and in the nature of comonomers (e.g. vinyl maleate) which are commonly used (see Section 14.4.4)... [Pg.389]

Recently, Li et al. [30], Yu et al. [31] reinvestigated the mechanism of graft copolymerization of vinyl monomers onto carbohydrates such as starch and cellulose initiated by the Ce(IV) ion with some new results as mentioned in Section II. Furthermore, they investigated the mechanism of model graft copolymerization of vinyl monomers onto chitosan [51]. They chose the compounds containing adjacent hydroxyl-amine structures, such as D-glucosamine, /mn5-2-amino-cyclohexanol, 2-... [Pg.551]

Reactions of this type are quite popular and widely used to introduce hydrophilic and ionogenic groups into linear polymers as well as directly into polymer networks. These reactions include hydrolysis (PAAm, PAAc and their analogs from PAN, PVA from poly (vinyl acetate), oxyethylation and oxymethylation of starch and cellulose, sulfurization, and other reactions. These processes are of industrial importance, well studied and widely reviewed. [Pg.110]

Carboxymethylcellulose, polyethylene glycol Combination of a cellulose ether with clay Amide-modified carboxyl-containing polysaccharide Sodium aluminate and magnesium oxide Thermally stable hydroxyethylcellulose 30% ammonium or sodium thiosulfate and 20% hydroxyethylcellulose (HEC) Acrylic acid copolymer and oxyalkylene with hydrophobic group Copolymers acrylamide-acrylate and vinyl sulfonate-vinylamide Cationic polygalactomannans and anionic xanthan gum Copolymer from vinyl urethanes and acrylic acid or alkyl acrylates 2-Nitroalkyl ether-modified starch Polymer of glucuronic acid... [Pg.12]

Fluid loss additives such as solid particles and water-thickening polymers may be added to the drilling mud to reduce fluid loss from the well bore to the formation. Insoluble and partially soluble fluid loss additives include bentonite and other clays, starch from various sources, crushed walnut hulls, lignite treated with caustic or amines, resins of various types, gilsonite, benzoic acid flakes, and carefully sized particles of calcium borate, sodium borate, and mica. Soluble fluid loss additives include carboxymethyl cellulose (CMC), low molecular weight hydroxyethyl cellulose (HEC), carboxy-methYlhydroxyethyl cellulose (CMHEC), and sodium acrylate. A large number of water-soluble vinyl copolymers and terpolymers have been described as fluid loss additives for drilling and completion fluids in the patent literature. However, relatively few appear to be used in field operations. [Pg.10]


See other pages where Vinyl starch is mentioned: [Pg.216]    [Pg.192]    [Pg.216]    [Pg.192]    [Pg.172]    [Pg.350]    [Pg.268]    [Pg.10]    [Pg.182]    [Pg.477]    [Pg.482]    [Pg.347]    [Pg.260]    [Pg.164]    [Pg.488]    [Pg.488]    [Pg.489]    [Pg.508]    [Pg.371]    [Pg.530]    [Pg.753]    [Pg.482]    [Pg.483]    [Pg.483]    [Pg.484]    [Pg.100]    [Pg.41]    [Pg.560]    [Pg.266]    [Pg.13]    [Pg.177]    [Pg.100]   
See also in sourсe #XX -- [ Pg.216 ]




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Acrylic acid-vinyl alcohol-starch graft

Ethylene-vinyl alcohol copolymer /thermoplastic starch

Starch vinyl acetate copolymer

Starch with ethylene vinyl alcohol

Starch/ethylene vinyl alcohol blend (SEVA

Vinyl acetate-starch graft copolymers

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