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Acrylates stability

Poly(vinyl acetate-co-acrylic), stabilized by nonionic surfactant. [Pg.845]

B-8880-50%. [Ethox] High m.w. polyoxyalkylene pdymer dyeing assistant for acrylics stabilizer for aq. emulsions. [Pg.42]

Ethyl acrylate, stabilized by addition of some hydroquinone, and dicobalt octa-carbonyl dissolved in benzene heated in a stirring V4A-steel autoclave to 250 under 160 atm. CO/H2, the pressure raised to ca. 300 atm., and stirring continued... [Pg.643]

Usually pH has to be adjusted with a suitable base, since the acrylate is a polyacid, to get an optimal extended polymer conformation [16] which leads to thickening of emulsions. Final emulsion viscosity depends on acrylate concentration and is independent of temperature control during preparation in contrast to common emulsions. In emulsions acrylate adsorbs at the oil/water interface at low concentrations of acrylate stabilization results from electro-steric effects and in the upper concentration range an associative thickening mechanism is postulated [17]. [Pg.91]

To optimize droplet size and to enhance emulsifying properties in acrylate-stabilized emulsions use of nonionic co-surfactants (sucrose esters) is proposed by Bobin et al. [19] who evaluated emulsions by means of rheology, miCTOSCOpy and pH measurements. [Pg.91]

A soln. of frans,frans-l,4-diacetoxy-l,3-butadiene and methyl acrylate stabilized with hydroquinone heated slowly to reflux in xylene, and the product isolated after 37 hrs. methyl 2j, 5) -diacetoxy-3-cyclohexene-la-carboxylate. Y 93%. E. E. Smissman et al., Am. Soc. 84, 1040 (1962). [Pg.424]

Unzueta and Forcada [93] developed a mechanistic model for the emulsion copolymerization of methyl methacrylate and n-butyl acrylate stabilized by mixed anionic and nonionic surfactants, which was verified by the experimental data. This model is based on the mass and population balances of precursor particles and the moments of particle size distribution. It is sensitive to such parameters as the composition of mixed surfactants and the total surfactant concentration. A competitive particle nucleation mechanism is incorporated into the model to successfully simulate the evolution of particle nuclei during polymerization. [Pg.90]

Chern and Hsu [19] extended the Novak model to the semibatch emulsion copolymerizations of methyl methacrylate and n-butyl acrylate stabilized by mixed anionic (sodium dodecyl sulfate) and nonionic (nonylphenol-40 units... [Pg.177]

Acryhc acid and esters are stabilized with minimum amounts of inhibitors consistent with stabihty and safety. The acryhc monomers must be stable and there should be no polymer formation for prolonged periods with normal storage and shipping (4,106). The monomethyl ether of hydroquinone (MEHQ) is frequentiy used as inhibitor and low inhibitor grades of the acrylate monomers are available for bulk handling. MEHQ at 10—15 ppm is generally... [Pg.156]

In normal practice, inhibitors such as hydroquinone (HQ) [123-31 -9] or the monomethyl ether of hydroquinone (MEHQ) [150-76-5] are added to acrylic monomers to stabilize them during shipment and storage. Uninhibited acrylic monomers should be used prompdy or stored at 10°C or below for no longer than a few weeks. Improperly iahibited monomers have the potential for violent polymerizations. HQ and MEHQ require the presence of oxygen to be effective inhibitors therefore, these monomers should be stored in contact with air and not under inert atmosphere. Because of the low concentration of inhibitors present in most commercial grades of acrylic monomers (generally less than 100 ppm), removal before use is not normally required. However, procedures for removal of inhibitors are available (67). [Pg.165]

Methylphenol is converted to 6-/ f2 -butyl-2-methylphenol [2219-82-1] by alkylation with isobutylene under aluminum catalysis. A number of phenoHc anti-oxidants used to stabilize mbber and plastics against thermal oxidative degradation are based on this compound. The condensation of 6-/ f2 -butyl-2-methylphenol with formaldehyde yields 4,4 -methylenebis(2-methyl-6-/ f2 butylphenol) [96-65-17, reaction with sulfur dichloride yields 4,4 -thiobis(2-methyl-6-/ f2 butylphenol) [96-66-2] and reaction with methyl acrylate under base catalysis yields the corresponding hydrocinnamate. Transesterification of the hydrocinnamate with triethylene glycol yields triethylene glycol-bis[3-(3-/ f2 -butyl-5-methyl-4-hydroxyphenyl)propionate] [36443-68-2] (39). 2-Methylphenol is also a component of cresyHc acids, blends of phenol, cresols, and xylenols. CresyHc acids are used as solvents in a number of coating appHcations (see Table 3). [Pg.67]

A large number of hindered phenoHc antioxidants are based on the Michael addition of 2,6-di-/ f2 -butylphenol and methyl acrylate under basic catalysis to yield the hydrocinnamate which is a basic building block used in the production of octadecyl 3-(3,5-di-/ f2 butyl-4-hydroxyphenyl)propionate, [2082-79-3], tetrakis(methylene-3(3,5-di-/ f2 butyl-4-hydroxylphenyl)propionate)methane [6683-19-8], and many others (63,64). These hindered phenolic antioxidants are the most widely used primary stabilizers in the world and are used in polyolefins, synthetic and natural mbber, styrenics, vinyl polymers, and engineering resins. 2,6-Di-/ f2 -butylphenol is converted to a methylene isocyanate which is trimerized to a triazine derivative... [Pg.69]

As a pharmaceutical, methyl salicylate is used in liniments and ointments for the relief of pain and for rheumatic conditions. As a flavor and fragrance agent, it is used in confectioneries, dentifrices, cosmetics, and perfumes. Other commercial applications for methyl salicylate are as a dye carrier, as a uv-light stabilizer in acrylic resins, and as a chemical intermediate. The May 1996 price was 5.50/kg (18). [Pg.289]

The principal solution to fabrication difficulties is copolymerization. Three types of comonomers are commercially important vinyl chloride acrylates, including alkyl acrylates and alkyimethacrylates and acrylonitrile. When extmsion is the method of fabrication, other solutions include formulation with plasticizers, stabilizers, and extmsion aids plus applying improved extmsion techniques. The Hterature on vinyHdene chloride copolymers through 1972 has been reviewed (1). [Pg.427]

New vinyl acetate—acrylate (VAA) emulsion copolymers stabilized with poly(vinyl alcohol) have been developed. The acryflc component of the VAAs contributes to improved compatibiUty with tackifiers (143). [Pg.469]

Resins are also used for permanent tooth-colored veneers on fixed prostheses, ie, crown and bridges. Compositions for this application include acryflcs, vinyl—acryflcs, and dimethacrylates, as well as silica- or quartz-microfilled composites. The resins are placed on the metallic substrates of the prostheses and cured by heat or light. These resins are inexpensive, easy to fabricate, and can be matched to the color of tooth stmcture. Acrylic facings do not chemically adhere to the metals and are retained only by curing the resin into mechanical undercuts designed into the metal substrate. They have relatively low mechanical strength and color stability, and poor abrasion and strain resistance they also deform more under the stress of mastication than porcelain veneers or facings. [Pg.490]

Low temperatures can cause a phase separation in stabilized solutions in which case one phase can become deficient in stabilizer and subject to runaway reactions. Acrylic acid can crystallize out of stabilized solution, and subsequent thawing of these essentially pure acrylic acid crystals can initiate runaway reactions, often with severe consequences. Thawing of crystallized (frozen) materials needs to be accomplished using established procedures in thaw boxes or similar devices. If established procedures are not available, a safety review needs to be conducted and a procedure developed prior to thawing the material. [Pg.107]

The demands on insulating materials in soil and fresh water are relatively low. Anodically evolved oxygen makes the use of aging-resistant insulating materials necessary. These consist of special types of rubber (neoprene) and stabilized plastics of polyethylene, and polyvinylchloride, as well as cast resins such as acrylate, epoxy, polyester resin and many others. [Pg.217]


See other pages where Acrylates stability is mentioned: [Pg.515]    [Pg.160]    [Pg.149]    [Pg.403]    [Pg.575]    [Pg.515]    [Pg.181]    [Pg.184]    [Pg.515]    [Pg.160]    [Pg.149]    [Pg.403]    [Pg.575]    [Pg.515]    [Pg.181]    [Pg.184]    [Pg.496]    [Pg.171]    [Pg.171]    [Pg.285]    [Pg.285]    [Pg.427]    [Pg.311]    [Pg.254]    [Pg.179]    [Pg.379]    [Pg.312]    [Pg.57]    [Pg.230]    [Pg.509]    [Pg.334]    [Pg.3]    [Pg.341]    [Pg.490]    [Pg.49]    [Pg.277]    [Pg.64]    [Pg.411]   
See also in sourсe #XX -- [ Pg.265 ]




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