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Latexes glass transition temperature

Macromolecular Symposia Vol.118, June 1997, p.267-73 THERMAL BEHAVIORS OF LATEXES WET LATEX GLASS TRANSITION TEMPERATURES... [Pg.114]

T and are the glass-transition temperatures in K of the homopolymers and are the weight fractions of the comonomers (49). Because the glass-transition temperature is directly related to many other material properties, changes in T by copolymerization cause changes in other properties too. Polymer properties that depend on the glass-transition temperature include physical state, rate of thermal expansion, thermal properties, torsional modulus, refractive index, dissipation factor, brittle impact resistance, flow and heat distortion properties, and minimum film-forming temperature of polymer latex... [Pg.183]

Polymeric binder can be added to the network either as an aqueous latex dispersion or as a solution that should be dried prior to lamination in this process. In either case, the polymer should form a film and join adjacent fibers together and thus improve the stress transfer characteristics of the fibrous network. Provided that the proper film forming conditions are available, the property profile of the bonded network is determined to a significant degree by the properties of the polymeric binder at the temperature of use [20,22]. For example, if a softer type of product is desired, a binder with a relatively low glass transition temperature Tg) is often chosen. [Pg.579]

The molecular weight, glass transition temperature (Tg) and size of dispersed polymer particles in the latexes can... [Pg.348]

Table 6.11 Effect of glass transition temperature Tg on the properties of acrylic-latex-modified mortar (Ma and Brown)... Table 6.11 Effect of glass transition temperature Tg on the properties of acrylic-latex-modified mortar (Ma and Brown)...
RESINS (Acrylonitrile-Butadiene-Styrene). Commonly referred to as ABS resins, these materials are thermoplastic resins which are produced by grafting styrene and acrylonitrile onto a diene-rubber backbone. The usually preferred substrate is polybutadiene because of its low glass-transition temperature (approximately —80°C). Where ABS resin is prepared by suspension or mass polymerization methods, stereospedfic diene rubber made by solution polymerization is the preferred diene. Otherwise, the diene used is a high-gel or cross-linked latex made by a hot emulsion process. [Pg.1436]

Formation of solubilized surfactant-latex complexes can influence the properties and performance of vinyl acrylic latexes prepared with NaLS and other penetrating type anionic surfactants. Such complexes seem to affect glass transition temperature and film coalescence process (12). [Pg.232]

The molecular weight, glass transition temperature (T) and size of dispersed polymer particles in the latexes can affect the strength and c loride ion permeability of latex-modified mortar and concrete to a certain extent [87,93] (Tables 6.11 and 6.12). SBR latexes with smaller particle size appear to initially provide lower chloride ion permeability to the mortars, but a difference in the permeability between the smaller and larger particle sizes eventually becomes insignificant as the concrete ages. The initial decrease in the permeability observed with smaller particles is attributed to the fact that smaller particle size coalesce into films faster than the larger particle sizes. [Pg.254]

Figure 7.23 Applications of the NMR-MOUSE to elastomer materials (a) T2 values for a curing series of carbon-black filled NR. Comparison of values obtained at high homogeneous field (DMX 300) and with the NMR-MOUSE, (b) cross-link series of unfilled SBR with different sulfur content, (c) T2 versus glass-transition temperature Tg of unfilled SBR by the CPMG and the steady-state CPMG methods, (d) normalized Hahn-echo decay curves for poly(butadiene) latex samples. Different decay rates are obtained for small medium and large cross-link densities... Figure 7.23 Applications of the NMR-MOUSE to elastomer materials (a) T2 values for a curing series of carbon-black filled NR. Comparison of values obtained at high homogeneous field (DMX 300) and with the NMR-MOUSE, (b) cross-link series of unfilled SBR with different sulfur content, (c) T2 versus glass-transition temperature Tg of unfilled SBR by the CPMG and the steady-state CPMG methods, (d) normalized Hahn-echo decay curves for poly(butadiene) latex samples. Different decay rates are obtained for small medium and large cross-link densities...
Inaba et al. prepared a series of model styrene/butyl acrylate copolymer latexes with glass transition temperatures at room temperature. The functional monomer 2-(3-isopropenylphenyl)-2-methylethylisocyanate (TMI) was used as monomer/crosslinking agent for further film formation. A small amount of methacrylic acid was introduced in some formulations in order to enhance the crosslinking reaction. A redox initiation system was used to reduce premature crosslinking during the polymerization [82]. [Pg.100]

Series I Acrylic Latex Emulsions. A series of four acrylic latex emulsions varying in glass transition temperature (Tg) (3) were applied first. Tg is the temperature at which the resin changes from a relatively flexible to a relatively stiff material. The acrylic latexes are made from water-insoluble monomers such as acrylates and alkyl acrylates polymerized in emulsion form to produce an aqueous dispersion or latex of the polymer. Upon drying, the emulsion is irreversibly broken so that the applied material becomes wash-fast. The application requires no catalyst or high temperature heating. [Pg.254]

In a related patent (46) Amagi et al. synthesized a triple latex IPN. In brief, polymer 1 was a crosslinked SBR, polymer 2 was a crosslinked styrene-methyl methacrylate copolymer, and polymer 3 was a crosslinked poly (methyl methacrylate). All three were sequentially synthesized on the same latex particle. The latex material was then mechanically blended with linear poly (vinyl chloride). Also, Torvik (47) blended together four polymers that had different glass transition temperatures. [Pg.176]

FIGURE 5 Glass transition temperature of plasticized ethylcellulose latex as a function of plasticizer type and concentration. Source From Ref. 69. [Pg.396]

Particle deformation and polymer diffusion can only occur at temperatures above the glass transition temperature of the polymer. Final coatings, however, are required to be at temperatures considerably below the glass transition temperature. To get around this problem, it is common to add plasticizers to water borne latex dispersions to lower the glass transition temperature of the constituent polymer during the film formation process. Subsequent evaporation of the plasticizer results in a hard final coating. A common plasticizer is 2,2,4-trimethyl-l,3-pentanediol monoisobutyrate, usually referred to as Texanol Ester Alcohol. [Pg.1453]

When designing a film forming latex dispersion, the properties to consider are the final mechanical properties of the film, as well as the ease of film formation The mechanical properties required, as well as the environment of operation will dictate the polymers suitable for the coating and may well dictate the glass transition temperature of the polymer. The crack points alluded to earlier correspond to the transition from capillary deformation to the receding water front regime. Therefore, a value of X less than 100 will ensure a well-formed film. [Pg.1454]

As previously mentioned, the properties of olefm-CO copolymers depend strongly on the nature of the olefin employed. The glass transition temperature of 1-olefin-CO copolymers decreases from room temperature to nearly -60 °C upon increasing the chain length of the 1-olefin from propylene to 1-dodecene [33]. By contrast to polar ethylene-CO copolymers, copolymers with higher l-olefins display a hydrophobic character. For 1-olefin copolymerization, catalysts with entirely alkyl-substituted diphosphine hgands R2P-(CH2) -PR2 (R=alkyl, by comparison to R=Ph in dppp) such as 3 are particularly well-suited [48]. Efhylene-l-olefin-CO terpolymers and 1-olefin-CO copolymers can be prepared in aqueous polymerizations [43, 47, 48]. In the aforementioned copolymerization reactions, the polyketone was reported to precipitate during the reaction as a sohd [45, 47, 48, 50]. However, in the presence of an emulsifier such as sodium dodecyl sulfate (SDS) and under otherwise suitable conditions, stable polymer latexes can be obtained. [Pg.241]

Most paint formulations consist of disperse systems (solid in liquid dispersions) [2]. The disperse phase consists of primary pigment particles (organic or inorganic) which provide the opacity, colour and other optical effects these are usually in the submicron range. Other coarse particles (mostly inorganic) are used in primers and undercoats to seal the substrate and enhance adhesion of the top coat The continuous phase consists of a solution of polymer or resin which provides the basis for a continuous film that seals the surface and protects it from the outside environment Most modem paints contain latexes which are used as film formers. These latexes - which typically have a glass transition temperature (Tg) below... [Pg.204]


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