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Acrylamides acrylonitriles

By using this technique acrylamide, acrylonitrile, and methyl acrylate were grafted onto cellulose [20]. In this case, oxidative depolymerization of cellulose also occurs and could yield short-lived intermediates [21]. They [21] reported an electron spin resonance spectroscopy study of the affects of different parameters on the rates of formation and decay of free radicals in microcrystalline cellulose and in purified fibrous cotton cellulose. From the results they obtained, they suggested that ceric ions form a chelate with the cellulose molecule, possibly, through the C2 and C3 hydroxyls of the anhy-droglucose unit. Transfer of electrons from the cellulose molecule to Ce(IV) would follow, leading to its reduction... [Pg.503]

Applications As the basic process of electron transfer at an electrode is a fundamental electrochemical principle, polarography can widely be applied. Polarography can be used to determine electroreductible substances such as monomers, organic peroxides, accelerators and antioxidants in solvent extracts of polymers. Residual amounts of monomers remain in manufactured batches of (co)polymers. For food-packaging applications, it is necessary to ensure that the content of such monomers is below regulated level. Polarography has been used for a variety of monomers (styrene, a-methylstyrene, acrylic acid, acrylamide, acrylonitrile, methylmethacrylate) in... [Pg.671]

Significant improvement in controlled polymerizations of a variety monomers, including styrene, acrylates, acrylamide, acrylonitrile, 1,3-dienes, and maleic anhydride has been achieved when alkoxyamines have been used as initiators for living, free radical polymerization.(696c, 697) Alkoxyamines can be easily synthesized in situ by the double addition of free radicals, generated by thermal decomposition of an azo-initiator, such as 2,2 -azo-h/.s-/.so-butyronitrile (AIBN), to nitrones (Scheme 2.206). [Pg.295]

A Determination of Carbonyl Compounds by HPLC 8316 Acrylamide, Acrylonitrile and Acrolein by HPLC... [Pg.1207]

Chloroethyl vinyl ether, 2-Chlorophenol, Cyclohexene, Dalapon-sodium. Diallate. 1,1-Dichloroethane, 2,3-Dimethylamine, Dimethylbutane, 1,4-Dioxane, Ethylamine, Ethyl ether, Erhvl sulfide. 2-Heptanone, Metaldehvde. 2-Methvlbutane. 2-Methvl-2-butene. 2-Methyl phenol, Nitromethane, 4-Nitrophenol, 2-Nitropropane, 1-Octene, 2-Pentanone, Phenol, Toluene, Triethylamine, Vinyl chloride, o-Xylene, m-Xylene Acetamide, see Acetonitrile, Acrylamide, Acrylonitrile, Ethylamine... [Pg.1518]

Hamann et al. (11) have prepared phenylazo-bound silica via four-step reactions from the starting silica (Aerosil 200) and carried out the polymerizations of styrene, methyl methacrylate, acrylamide, acrylonitrile, acrylic acid, and 4-vinylpyri-... [Pg.628]

Commission Recommendation of 29 April 2004 on the results of the risk evaluation and the risk reduction strategies for the substances acetonitrile acrylamide acrylonitrile acrylic acid butadiene hydrogen fluoride hydrogen peroxide methacrylic acid methyl methacrylate toluene trichlorobenzene (2004/394/EC) 30.4.2004, Official Journal of the European Union, EC, 2004, No.L.144. [Pg.330]

Bicyclobutanes activated by bridgehead cyano group undergo copolymerization with various monomers such as vinyl chloride, acrylamide, acrylonitrile and styrene ... [Pg.1178]

As various organic monomers, such as acrylamide, acrylonitrile, vinyl acetate, maleic acid and styrene, can polymerize at the same time as forming inorganic nanomaterials, various kinds of polymer-inorganic nanocomposites can be prepared at room temperature by a y-irradiation synthesis method. [Pg.202]

Tetrachlorodibenzo-/)-dioxin Thorium(IV) oxide Triethylenethiophosphoramide Reasonably Anticipated to be Human Carcinogens Acetaldehyde 2-(Acetylamino)fluorene Acrylamide Acrylonitrile... [Pg.2418]

Acrylamide + acrylonitrile Resin Water Ammonium persulfate Atm 165-175 ... [Pg.262]

Values of are, however, more likely to be above or below unity, and curve n of Figure 5.1 represents the nearly ideal pair acrylamide + acrylonitrile, for which r,r2 = 1.17. This shows the slight deviation from ideal copolymeiization and illustrates the use of the curve as a guide to the composition drift, which can be expected when r, r-. ... [Pg.125]

Most of the water-soluble monomers, such as the acrylic and methacrylic acids, are functional monomers and are covered in Section 6.2.3. In Table 6.1 the most water-soluble monomers are acrylamide, acrylonitrile, methyl acrylate and vinyl acetate. Acrylamide contains two reactive centres. The amide group undergoes the reactions characteristic to aliphatic amides. For this reason, acrylamide may be considered as a functional monomer. Copolymerization of acrylamide with other monomers is often done to incorporate hydrophilic centres in oleophylic polymers to promote adhesion and dye acceptance. The monomer is available either as a solid or as a 50% aqueous solution. The latter is the preferred form, since it eliminates handling of a solid. The monomer is a neurotoxin and exposure to skin or inhalation must be prevented. Acrylamide solution is stabilized with cupric ions. Cupric ion availability is pH dependent and the pH must be between 5.2 and 6. Storage temperature should be between 16 and 32 °C... [Pg.119]

A variety of monomers have been successfully polymerized using ATRP [24], Typical monomers include (meth)acrylates, (meth)acrylamides, acrylonitrile, and styrenes as shown in Fig. 3.3. [Pg.25]

NMP [191-193] can be applied to a wide range of monomers such as styrenes, acrylates, acrylamides, acrylonitrile, and 1,3-dienes. Acyclic nitroxides such as 2,2,5-trimethyl-4-phenyl-3-azahexane-3-nitroxide (TIPNO) or Af-tert-butyl-iV-(l-diethyl phosphono-2,2-dimethylpropyl) nitroxide (DEPN) enables the reversible termination of the growing polymer chains. [Pg.26]

Diethylene glycol bis (allyl carbonate) monomer, organic synthesis Methacrylic acid monomer, organic synthetic Vinyl chloride monomer, paints Acrylamide Acrylonitrile 2-Hydroxyethylethylene urea Methyl methacrylate Styrene Vinyl chloride Vinyltoluene monomer monomer, paints/coatings 3,3,5-Trimethylcyclohexyl methacrylate monomer, photographic reproductive toners Dicyclopentenyl methacrylate 2-Phenoxyethyl methacrylate 3,3,5-Trimethylcyclohexyl methacrylate... [Pg.5476]

Quatemized copolymers of vinyl pyrrolidone and dimethylaminoethylthacrylate, which is cationic, have been developed for the hair care and skin care industries because of their optimal substantivity, minimum buildup, and ability to form nontacky and continuous films. Other important comonomers include vinyl alcohol, styrene, maleic anhydride, acrylamide, acrylonitrile, crotonic acid, and methyl methacrylate. [Pg.312]

Determination of intermediates in dye synthesis (anthraquinone and derivatives), azo dyes in intermediates, products, coloring solutions and industrial effluents. Determination of aggregation number of textile dyes. Determination of food colors (e.g., of tartrazine type) in soft drinks Determination of monomers (aldehydes, acrylamide, acrylonitrile, isocyanates, methyl methacrylate, styrene, vinyl acetate) in final products and industrial effluents. Determination of initiators (azodiisobutyinitrile, benzoyt peroxide, cyclohexylperoxydicarbonate, laurylperoxide), inhibitors (hydroquinones, butylated hydroxyanisole, 4-f-butyl phenolsulphide, AAphenyt- -naphthylamine) and organo-tin stabilizers in PVC plastics... [Pg.3762]

Toxic in contact with skin 3 Danger >200 to <1000 Acrolein, acrylamide, acrylonitrile, aniline, t-butylhydroperoxide, ethylene dibromide, formaldehyde, hydrogen peroxide, methyl iodide, phenol... [Pg.363]

Paper coating Styrene butadiene plus polar monomers Core styrene butadiene Shell acrylic acid, acrylamide, acrylonitrile Increased water resistance and higher gloss... [Pg.3763]

Results of the Risk Evaluation and the Risk Reduction Strategies for the Substances Acetonitrile Acrylamide Acrylonitrile Acrylic acid Butadiene Hydrogen fluoride Hydrogen peroxide Methacrylic acid Methyl methacrylate Toluene Trichlorobenzene. (notified under document number C(2004) 1446) (Text with EEA relevance) (2004/394/EC). Available at http //esis.jrc.ec.europa.eu/doc/risk assess-ment/OJ RECOMMENDAT10N / ojrecl08883.pdf (accessed October 25,2013). [Pg.133]

To detect acrylamide in aqueous matrices, the EPA-OSW method is GC in combination with electron capture detector (ECD) [35]. The detection level is 0.032 pg/L. Method 8316 of EPA-OSW deals with the high-performance liquid chromatographic determination of acrylamide, acrylonitrile, and acrolein in water. Detection is in UV-mode LOD is 10 pg/L. [43]. [Pg.741]

Iso-Butyl Acrylate Methyl Acrylate Acrolein Acrylamide Acrylonitrile Charcoal I-Dodecene Adipic Acid Dioctyl Adipate... [Pg.127]

Adipic acid dimethyi adipate (polyesters), acrylamide (acrylonitrile co-polymers), acrylonitrile (acrylamide co-polymers), acrylic acid (acrylic polymers), buta-1,3-dlene (PS co-polymers, elastomers), butan-1,4-diol (polyesters), 2,2-bis(4-hydroxyphenyl)butan-1-ol (polyesters), 1,1-bis(4-hydroxyphenyl)cyclohexane (polyesters), 4,4 -(propane-2,2-diyl)-dlphenol known as bisphenol A (polyesters), ethyleneglycol (polyestere), formaldehyde (phenol-formaldehyde resins), isophthalic acid (PET), caprolactame and C -C,2 aminocar-boxyllc acids and their lactames (polyamides), melamine (amino-formaldehyde resins), methacryllc acid and methyl methacrylate (acrylic polymers), methylstyrene (PS and co-polymers), propyleneglycol (polyesters), sebacic acid and dimethyl sebacate (polyesters), styrene (PS and co-polymers), terephthalic acid and dimethyl terephthalate (PET), vinyl acetate (vinyl acetate co-polymers), vinyl chloride (PVC and co-polymers), vinylldenechlorlde (PVdC and co-polymers)... [Pg.1048]

Plastic foams Acrylamide Acrylonitrile Netherlands 3,715 1968 Stamicarbon N.V. ... [Pg.523]


See other pages where Acrylamides acrylonitriles is mentioned: [Pg.43]    [Pg.489]    [Pg.109]    [Pg.421]    [Pg.53]    [Pg.36]    [Pg.164]    [Pg.540]    [Pg.253]    [Pg.301]    [Pg.306]    [Pg.641]    [Pg.178]    [Pg.489]    [Pg.268]    [Pg.146]    [Pg.372]    [Pg.675]    [Pg.1162]    [Pg.6929]    [Pg.625]    [Pg.84]    [Pg.1162]    [Pg.629]   
See also in sourсe #XX -- [ Pg.355 ]




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Acrylamide, from acrylonitrile

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