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Reactive emulsifier

The emulsifier provides sites for the particle nucleation and stabilizes growing or the final polymer particles. Even though conventional emulsifiers (anionic, cationic, and nonionic) are commonly used in emulsion polymerization, other non-conventional ones are also used they include reactive emulsifiers and amphiphilic macromonomers. Reactive emulsifiers and macromonomers, which are surface active emulsifiers with an unsaturated group, are chemically bound to the surface of polymer particles. This strongly reduces the critical amount of emulsifier needed for stabilization of polymer particles, desorption of emulsifier from particles, formation of distinct emulsifier domains during film formation, and water sensitivity of the latex film. [Pg.13]

Instead of conventional surfactant molecules, amphiphilic water soluble macromonomers, especially PEO macromonomers, have been used extensively as a reactive emulsifier and as steric stabilizer polymer, as summarized in Table 5. Generally speaking, however, the mechanism for the particle nucleation in the emulsion polymerization systems using macromonomers has been poorly established when compared to the dispersion copolymerizations with macromonomers as mentioned earlier. [Pg.168]

Synonyms 2-Methyl-2-propene-1-sulfonic acid sodium salt Empiricai C4H7NaO S Formuia H2C=C(CH3)CH2S03Na Properties M.w. 158.15 m.p. > 300 C anionic Uses Dye improver reactive comonomer for acrylic fibers polymerization dyeable polyacrylonitrile/polyvinyl acetate comonomer reactive emulsifier or coemulsifier Manuf./Distrib. Aldrich http //www.sigma-aidrich.com, Monomer-Polymer Dajac Labs Trade Name Synonyms Geropon MLS/A [Rhodia HPCII http //www.rhodia-hpcii.com]... [Pg.4066]

Preferred monomers are alkyl (meth)acrylates, such as butyl acrylate, acrylic acid, and y-methacryloxypropyl triethoxysilane. A reactive emulsifier is used which refers to an emulsifier that has an emulsifying capability and is radically polymerizable. [Pg.162]

Thus, the reactive emulsifier is a compoimd that has a hydrophilic group, e.g., a sulfuric ester, a hydrophobic group, e.g., aliphatic alkyl or aromatic groups, and a radically reactive group, e.g., allyloxy and propenyl groups. [Pg.163]

Specific examples of suitable reactive emulsifiers are shown in Table 5.8. [Pg.163]

MAIs may also be formed free radically when all azo sites are identical and have, therefore, the same reactivity. In this case the reaction with monomer A will be interrupted prior to the complete decomposition of all azo groups. So, Dicke and Heitz [49] partially decomposed poly(azoester)s in the presence of acrylamide. The reaction time was adjusted to a 37% decomposition of the azo groups. Surface active MAIs (M, > 10 ) consisting of hydrophobic poly(azoester) and hydrophilic poly(acrylamide) blocks were obtained (see Scheme 22) These were used for emulsion polymerization of vinyl acetate—in the polymerization they act simultaneously as emulsifiers (surface activity) and initiators (azo groups). Thus, a ternary block copolymer was synthesized fairly elegantly. [Pg.745]

Using magnesium ether carboxylates as emulsifier a porous polyvinylchloride can be made [218] and a propoxylated ether carboxylate is described as emulsifier to make an ethyl acrylate-styrene copolymer [219]. A crosslinked latex with a three-dimensional network is achieved by polymerizing an ethylenically unsaturated monomer with a reactive saturated monomer using ether carboxylate as emulsifier [220]. [Pg.345]

Therefore, there is substantial evidence that GA can play a positive health-related role in addition to its well-known properties as an emulsifier. Therefore, the aim of this chapter is to describe general aspects of the source, composition, and already known uses of GA as well as some new aspects of its antioxidant capacity against some reactive oxygen substances (ROS), and its antimicrobial activity (AMA). [Pg.3]

For studying the emulsifying properties, saturated polyesters can be used to avoid complications by the reactivity of unsaturated units of the EUP [117]... [Pg.161]

Elastomers with reactive end groups such as maleic anhydride (MA) or glycidyl methacrylate (GMA) are preferred for toughening PET. The reason that they are so effective is that they form a graft copolymer by reaction with the PET hydroxyl and carboxyl end groups (as shown below). The graft copolymer then acts as an emulsifier to decrease the interfacial tension and reduce the tendency... [Pg.509]

Although not a telomerization, it is mentioned here, that syndiotactic 1,2-polybutadienes were prepared in aqueous emulsions with a 7t-allyl-cobalt catalyst [33]. Similarly, chloroprenes were polymerized using aqueous solutions of [PdCl2(TPPMS)2] and [RhCl(TPPMS)3] as catalysts at 40 °C in the presence of an emulsifier and a chain growth regulator (R-SH, R=Cio-Cis) [35]. Despite the usual low reactivity of chlorinated dienes, these reactions proceeded surprisingly fast, leading to quantitative conversion of 10 g chloroprene in 2 hours with only 50 mg of catalyst (approximate TOP = 3500 h- ). [Pg.198]

B.E.S.T. has several potential limitations. System performance can be influenced by the presence of detergents and emulsifiers, which can adversely affect oil/water phase separation. Because some solvents cannot exist in a liquid state in media with a pH of less than 10, performance can also be affected by alkaline feed material. Depending on the compounds present, some sludges may be reactive with the solvent under alkaline conditions. Elevated levels of volatiles can also be chemically reactive with amine solvents. In addition, some solvents used in the process, such as triethylamine (TEiA), are flammable in oxygenated environments. [Pg.917]

Milk containing fat globules with a natural fat globule membrane can be activated, deactivated, and reactivated by proper changes in temperature. However, some loss of activity will occur upon repeated activation (Wang and Randolph 1978). The phenomenon of temperature activation is found only when the fat globules have their natural layer of adsorbed materials. Neither homogenized milk, nor emulsions of tributyrin, nor butter oil emulsified in skim milk can be activated in this manner. [Pg.226]

In the manufacture of unsaturated polyester resins the polyester is synthesized and then diluted with a vinyl reactive monomer such as styrene (see POLYESTERS, UNSATURATED). A portion of the dibasic acid of the polyester is maleic or some other vinyl reactive diacid that can be polymerized with the styrene to yield a highly cross-linked, high performance polymer system. Other esters made with propylene glycol, dipropylene glycol, and tripropylene glycol are used as emulsifiers in foods, as plasticizers in polymer systems, and as part of acrylate resin systems. [Pg.366]

The formulation ofmoisture-ujriiig silicones includes a silicone polymer, filler, a moisture-reactive cross-linker, and sometimes a catalyst. A newer class of silicone sealants are known as the silicone latex sealants. These sealants are silicone-in-water emulsions that cure by evaporation of the emulsifying water. Addition-curing silicones in general are two-part systems that cure by the platinum-catalyzed reaction of a silicone hydride with typically a vinyl group attached to silicon. Because no by-products are generated by the cure, there are few volatiles and no shrink in thick sections. [Pg.1462]

Even when the presence of homopolymer is not detrimental for the subsequent application of the graft copolymer as an emulsifying agent for the two homopolymers, high values for e are desirable. However, s values > 50% have only been achieved in a few special cases where the low-molar-mass radical is less reactive with respect to the monomer than the, simultaneously produced, polymer radical32,33,36,41 (see Table 3.16). [Pg.173]


See other pages where Reactive emulsifier is mentioned: [Pg.601]    [Pg.215]    [Pg.52]    [Pg.136]    [Pg.157]    [Pg.41]    [Pg.162]    [Pg.163]    [Pg.57]    [Pg.601]    [Pg.215]    [Pg.52]    [Pg.136]    [Pg.157]    [Pg.41]    [Pg.162]    [Pg.163]    [Pg.57]    [Pg.191]    [Pg.366]    [Pg.441]    [Pg.18]    [Pg.19]    [Pg.61]    [Pg.520]    [Pg.464]    [Pg.310]    [Pg.221]    [Pg.53]    [Pg.147]    [Pg.160]    [Pg.160]    [Pg.252]    [Pg.73]    [Pg.165]    [Pg.19]    [Pg.24]    [Pg.158]    [Pg.21]    [Pg.218]   
See also in sourсe #XX -- [ Pg.162 ]




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