Acrylic acid Butadiene

Later, Kang et al. [35] reported surface modification of carbon black using various monomers like acetylene, acrylic acid, butadiene, and oxygen. They concluded that it is possible to manipulate the surface properties of carbon black using plasma polymerization. 

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. 

The polar component increased exponentially with growing concentration of OH or COOH groups in the plasma copolymers of allyl alcohol-ethylene, allyl alcohol-butadiene or acrylic acid-butadiene precursors (Fig. 18.5). Low concentrations of OH or COOH groups produce only a very small polar component (Fig. 18.5). It is assumed that in this case the functional groups at the polymer surface are oriented toward the bulk, and thus do not contribute to the polar component... 

Copoly(Acrylic Acid - Butadiene) Copoly(Propylene Oxide - Tetrahydrofuran) P 631-2822... 

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). 

Gel-formation by reaction of acrylic acid-butadiene co-oligomers with saccharides and related hydroxylated compounds [130]. 

Acrylonitrile is mainly used to produce acrylic fibers, resins, and elastomers. Copolymers of acrylonitrile with butadiene and styrene are the ABS resins and those with styrene are the styrene-acrylonitrile resins SAN that are important plastics. The 1998 U.S. production of acrylonitrile was approximately 3.1 billion pounds. Most of the production was used for ABS resins and acrylic and modacrylic fibers. Acrylonitrile is also a precursor for acrylic acid (by hydrolysis) and for adiponitrile (by an electrodimerization). 

A lower max response at resonance was noted for poly butadiene-acrylic acid-containing pro-pints compared with polyurethane-containing opaque proplnts. Comparison of the measured response functions with predictions of theoretical models, which were modified to consider radiant-heat flux effects for translucent proplnts rather than pressure perturbations, suggest general agreement between theory and expt. The technique is suggested for study of the effects of proplnt-formulation variations on solid-proplnt combustion dynamics... 

CA 63,17781 (1965) Proplnt failure characteristics were measured in uniaxial and biaxial stress states for poly butadiene acrylic acid and Nitroplastisol proplnts, and failure conditions were examined over a wide range of temps. The observed failure conditions were compared for various failure criteria, and it was found that a... 

A modified latex composition contains a phosphorus surface group. Such a latex is formed by emulsion polymerization of unsaturated synthetic monomers in the presence of a phosponate or a phosphate which is intimately bound to the surface of the latex. Thus, a modified latex containing 46% solids was prepared by emulsion polymerization of butadiene, styrene, acrylic acid-styrene seed latex, and a phosphonate comonomer in H20 in the presence of phosphated alkylphenol ethoxylate at 90°C. The modified latex is useful as a coating for substrates and as a binder in aqueous systems containing inorganic fillers employed in paper coatings, carpet backings, and wallboards [119]. 

Brandt [200] has extracted tri(nonylphenyl) phosphite (TNPP) from a styrene-butadiene polymer using iso-octane. Brown [211] has reported US extraction of acrylic acid monomer from polyacrylates. Ultrasonication was also shown to be a fast and efficient extraction method for organophosphate ester flame retardants and plasticisers [212]. Greenpeace [213] has recently reported the concentration of phthalate esters in 72 toys (mostly made in China) using shaking and sonication extraction methods. Extraction and analytical procedures were carefully quality controlled. QC procedures and acceptance criteria were based on USEPA method 606 for the analysis of phthalates in water samples [214]. Extraction efficiency was tested by spiking blank matrix and by standard addition to phthalate-containing samples. For removal of fatty acids from the surface of EVA pellets a lmin ultrasonic bath treatment in isopropanol is sufficient [215]. It has been noticed that the experimental ultrasonic extraction conditions are often ill defined and do not allow independent verification. 

Partially saponified poly(vinyl acetate) Fully saponified poly(vinyl acetate) Copolymers with crotonic acid Copolymers with vinyl acetate with methacrylic acid with acrylic acid esters with acrylonitrile with styrene with ethyl vinyl ether with butadiene... 

Specific design considerations for a few substances including acrylic acid, styrene, organic peroxides, ethylene oxide, and 1,3-butadiene are given in CCPS (1995) on the basis of an industiy-practice survey. Detailed information for other substances is distributed by industry... 

POLYMERIZING Has the tendency to self-react to form larger molecules, while possibly generating enough heat/gases to burst a container Acrylic acid, styrene, 1,3-butadiene... 

Emulsion paints are based on aqueous synthetic resin dispersions, which afford a lacquer-like paint film. The resin dispersions which are commonly used by the paint industry contain water as the carrier phase. A large number of such dispersions are available, based on different resins such as poly(vinyl acetate), which may be employed as a copolymer with vinyl chloride, maleic dibutyl ester, ethylene, acrylic acid esters, polyacrylic resin, and copolymers of the latter with various monomers, as well as styrene-butadiene or poly(vinyl propionate). These disper-... 

However, the two syntheses of Tamiflu, involving two potentially hazardous azide-containing intermediates, need further improvements. A recently published short and enantioselective pathway starting from acrylic acid and 1,3-butadiene looks promising [47]. 

Acrylic acid, Initiator, Water, 1148 Aluminium chloride, Water, 0062 Barium peroxide, Propane, 0216 1,3-Benzodithiolium perchlorate, 2677 1,1 -Bis(fluorooxy)tetrafluoroethane, 0641 Borane-tetrahydrofuran, 0138 Boron tribromide, Water, 0122 Bromine, Aluminium, Dichloromethane, 0261 Bromine, Tungsten, Tungsten trioxide, 0261 f 1,3-Butadiene, 1480 Calcium oxide, Water, 3937 Chlorine trifluoride, Refractory materials, 3981 Chromium trioxide, Acetic acid, 4242 Copper(II) oxide, Boron, 4281 Diazoacetonitrile, 0675 Dihydroxymaleic acid, 1447 Ethyl azide, 0872... 

List C contains peroxidisable monomers, where the presence of peroxide may initiate exothermic polymerisation of the bulk of material. Precautions and procedures for storage and use of monomers with or without the presence of inhibitors are discussed in detail. Examples cited are acrylic acid, acrylonitrile, butadiene, 2-chlorobutadiene, chlorotrifluoroethylene, methyl methacrylate, styrene, tetraflu-oroethylene, vinyl acetate, vinylacetylene, vinyl chloride, vinylidene chloride and vinylpyridine [1]. 

This molecule, CH2 = C - CN, is copolymerized with acrylic acid, styrene, maleic anhydride, butadiene, or is op re ne to produce a wide variety of plastics and coatings. 

Monomers which can add to their own radicals are capable of copolymerizing with SO2 to give products of variable composition. These include styrene and ring-substituted styrenes (but not a-methylstyrene), vinyl acetate, vinyl bromide, vinyl chloride, and vinyl floride, acrylamide (but not N-substituted acrylamides) and allyl esters. Methyl methacrylate, acrylic acid, acrylates, and acrylonitrile do not copolymerize and in fact can be homopolymer-ized in SO2 as solvent. Dienes such as butadiene and 2-chloro-butadiene do copolymerize, and we will be concerned with the latter cortpound in this discussion. 

Many substituents stabilize the monomer but have no appreciable effect on polymer stability, since resonance is only possible with the former. The net effect is to decrease the exothermicity of the polymerization. Thus hyperconjugation of alkyl groups with the C=C lowers AH for propylene and 1-butene polymerizations. Conjugation of the C=C with substituents such as the benzene ring (styrene and a-methylstyrene), and alkene double bond (butadiene and isoprene), the carbonyl linkage (acrylic acid, methyl acrylate, methyl methacrylate), and the nitrile group (acrylonitrile) similarly leads to stabilization of the monomer and decreases enthalpies of polymerization. When the substituent is poorly conjugating as in vinyl acetate, the AH is close to the value for ethylene. 

Commercial barrier resins which are used as packaging films and blown bottles are produced by blending copolymers of acrylonitrile, ethyl acrylate, and butadiene with selected copolymers of acrylonitrile. These barrier resins have a Tg of about 125 C, a coefficient of linear expansion of 6.7 X 10 5 cm/cm C, a heat deflection temperature of 77 C, and an index of refraction of 1.511. These resins are resistant to nonoxidizing alkalis and acids and are decomposed by mineral acids. 

A terpolymer of butadiene, acrylonitrile, and acrylic acid can be made by similar procedures developed for the copolymer. Substitution of this terpolymer in propellant formulation results in a higher modulus and a greater resistance to creep without appreciable sacrifice of strain capability except at temperatures below ambient. 

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