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Butyl cellulose

OSE As butylating agent in Organic synthesis, e.g., in the uuuiuf of butyl cellulose. [Pg.239]

Ethyl cellulose butyl cellulose butyl carbitol acetate terpineol ZnO Cu Deore et al. (2011)... [Pg.253]

As of 1996, the production plant at Monsanto was still pilot-scale. Typical properties of Versicon were Compacted powder conductivity 4 S/cm, moisture 4% w/w, particle size 3 - 100 /i, density 1.36 g/cc, surface area 5-20 m /g. Also produced on a pilot scale by Monsanto was a "soluble P(ANi) , a green liquid which is a blend of 50% colloidal P(ANi), 40% xylenes and 10% butyl cellulose. P(ANi) was at one time also marketed by AmeriChem, Inc., Cleveland, OH, USA, in collaboration with Monsanto, and by PolySciences Inc., Pittsburgh, PA, USA. Other dispersions of P(ANi) in PVC, Nylon-12, and other thermoplastics were also, in the mid-1990 s, in the test marketing stage in collaboration with Zipperling Kessler Co.. [Pg.140]

PVF resins are generally compatible with phthalate, phosphate, adipate, and diben2oate plastici2ers, and with phenoHc, melamine—formaldehyde, urea—formaldehyde, unsaturated polyester, epoxy, polyurethane, and cellulose acetate butylate resins. They are incompatible with polyamide, ethyl cellulose, and poly(vinyl chloride) resins (141). [Pg.455]

Citric acid esters are used as plasticizers ia plastics such as poly(viayl chloride), poly(vinhdene chloride), poly(viQyl acetate), poly(viQyl butyral), polypropylene, chlorinated rubber, ethylceUulose, and cellulose nitrate. Most citrate esters are nontoxic and are acceptable by the FDA for use in food-contact packaging and for flavor in certain foods. As a plasticizer, citrate esters provide good heat and light stabiUty and excellent flexibiUty at low temperatures. Triethyl citrate, tri- -butyl citrate, isopropyl citrate, and stearyl citrate are considered GRAS for use as food ingredients (224—228). [Pg.187]

The acetates of most alcohols are also commercially available and have diverse uses. Because of their high solvent power, ethyl, isopropyl, butyl, isobutyl, amyl, and isoamyl acetates are used in ceUulose nitrate and other lacquer-type coatings (see Cellulose, esters). Butyl and hexyl acetates are exceUent solvents for polyurethane coating systems (see Coatings Urethane polymers). Ethyl, isobutyl, amyl, and isoamyl acetates are frequentiy used as components in flavoring (see Flavors and spices), and isopropyl, benzyl, octyl, geranyl, linalyl, and methyl acetates are important additives in perfumes (qv). [Pg.374]

Plasticizers can be classified according to their chemical nature. The most important classes of plasticizers used in rubber adhesives are phthalates, polymeric plasticizers, and esters. The group phthalate plasticizers constitutes the biggest and most widely used plasticizers. The linear alkyl phthalates impart improved low-temperature performance and have reduced volatility. Most of the polymeric plasticizers are saturated polyesters obtained by reaction of a diol with a dicarboxylic acid. The most common diols are propanediol, 1,3- and 1,4-butanediol, and 1,6-hexanediol. Adipic, phthalic and sebacic acids are common carboxylic acids used in the manufacture of polymeric plasticizers. Some poly-hydroxybutyrates are used in rubber adhesive formulations. Both the molecular weight and the chemical nature determine the performance of the polymeric plasticizers. Increasing the molecular weight reduces the volatility of the plasticizer but reduces the plasticizing efficiency and low-temperature properties. Typical esters used as plasticizers are n-butyl acetate and cellulose acetobutyrate. [Pg.626]

Nitro-filter cloths are composed of cellulose nitrate, which is an ester of cellulose. Any chemical compound that will saponify the ester will destroy the cloth. Caustic soda or potash in strengths of 2% at 70° C or over alkali sulfides, polysulfides and sulfohydrates or mixtures of ethyl alcohol and ether, ethyl, amyl and butyl acetates, pyridine, ferrous sulfates, and other reducing agents are detrimental to the cloth. [Pg.127]

Acetic acid is a versatile reagent. It is an important esterifying agent for the manufacture of cellulose acetate (for acetate fibers and lacquers), vinyl acetate monomer, and ethyl and butyl acetates. Acetic acid is used to produce pharmaceuticals, insecticides, and dyes. It is also a precursor for chloroacetic acid and acetic anhydride. The 1994 U.S. production of acetic acid was approximately 4 billion pounds. [Pg.240]

Polyisobutylene Cellulose acetate Poly(ethyl methacrylate) Poly(butyl methacrylate)... [Pg.27]

Okamoto et al [85] performed the optical resolution of primaquine and other racemic drugs by high performance liquid chromatography using cellulose and amylose tris-(phenylcarbamate) derivatives as chiral stationary phases. Primaquine and other compounds were effectively resolved by cellulose and/or amylose derivatives having substituents such as methyl, tertiary butyl, or halogen, on the phenyl groups. [Pg.190]

Lamellar, single crystals of cellulose triacetate, precipitated from nitromethane with butyl alcohol, were studied by X-ray and electron diffraction. Only the crystals containing the mother liquor, or moistened with nitromethane, showed rich diffraction details. From stretched and annealed fibers, it was found that the unit cell is tetragonal, with a = fe = 21.15A (2.115 nm), and c = 41.36 A (4.136 nm). [Pg.397]

Fig. 5.2 The main crop-to-energy chains. BtL Biomass-to-Liquid, GtL Gas-to-Liquid, ETBE Ethyl tert-butyl ether, MTBE Methyl tert-butyl ether, MeOH Methanol, DME Dimethyl ether. Pyrolysis oil, HTU-Diesel (Hydro Thermal Upgrading), ethanol and hydrogen from ligno-cellulosic species are not considered here because of their minor practical relevance in the near future... Fig. 5.2 The main crop-to-energy chains. BtL Biomass-to-Liquid, GtL Gas-to-Liquid, ETBE Ethyl tert-butyl ether, MTBE Methyl tert-butyl ether, MeOH Methanol, DME Dimethyl ether. Pyrolysis oil, HTU-Diesel (Hydro Thermal Upgrading), ethanol and hydrogen from ligno-cellulosic species are not considered here because of their minor practical relevance in the near future...
Uncharged styryl (methine) disperse dyes were originally introduced to provide greenish yellow colours on cellulose acetate fibres. One such dye still in use is Cl Disperse Yellow 31 (6.226), which is made by condensing 4-(N-butyl-N-chloroethylamino)benzaldehyde with ethyl cyanoacetate. Suitable compounds for polyester usually contain the electron-accepting dicyanovinyl group, introduced with the aid of malononitrile. An increased molecular size leads to improved fastness to sublimation, as in the case of Cl Disperse Yellow 99 (6.227). A novel polymethine-type structure of great interest is present in Cl Disperse Blue 354 (6.228), which is claimed to be the most brilliant blue disperse dye currently available [85]. [Pg.350]

Full dissolution has been reported to proceed in ionic liquids such as butyl- or allyl-methyl-imidazolium chloride under microwave irradiation [59, 60], The Clanton is claimed to be essential to favor the de-agglomerization of the cellulose by breaking its H-bonds that hold it together [61]. The cellulose can subsequently be precipitated from the ionic liquid upon addition of, for example, water, without significant depolymerization. [Pg.40]

Among the methacrylates, methyl and ethyl ester can be the most easily polymerized by the uncatalyzed polymerization. This specificity was a conclusion (25) which was obtained in the uncatalyzed polymerization initiated with silk or cellulose. Also in the cases of PVPA (23) and starch (26) the same specificity was observed, as shown in Table 6. n-Butyl ester was always hardly polymerized. [Pg.112]

Subsequent tests in which small portions of these undiluted liquid amines and dried cellulose nitrate linters were contacted (with a little added butyl acetate for the solid phenol) under various conditions, gave ignition with the first 3 amines, and exotherms to 110°C with foaming decomposition for the remaining 4. Other amine resin components showed slight or no exotherms in either test [2], Contact of cellulose nitrate with a little butylamine caused explosive reaction [3]. [Pg.85]


See other pages where Butyl cellulose is mentioned: [Pg.610]    [Pg.4929]    [Pg.283]    [Pg.321]    [Pg.391]    [Pg.52]    [Pg.2005]    [Pg.610]    [Pg.4929]    [Pg.283]    [Pg.321]    [Pg.391]    [Pg.52]    [Pg.2005]    [Pg.72]    [Pg.94]    [Pg.41]    [Pg.364]    [Pg.249]    [Pg.257]    [Pg.102]    [Pg.544]    [Pg.432]    [Pg.927]    [Pg.21]    [Pg.253]    [Pg.115]    [Pg.115]    [Pg.131]    [Pg.74]    [Pg.85]    [Pg.304]    [Pg.306]    [Pg.113]    [Pg.17]    [Pg.405]    [Pg.406]    [Pg.56]   
See also in sourсe #XX -- [ Pg.52 ]




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Cellulose acetate butylate

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