Poly , latex particle

Partially hydrolyzed poly(vinyl alcohol) grades are preferred because they have a hydrophobic /hydrophilic balance that make them uniquely suited for emulsion polymerization. The compatibUity of the residual acetate units with the poly(vinyl acetate) latex particles partly explains the observed stabilization effect. The amount of PVA employed is normally 4—10% on the weight of vinyl acetate monomer. The viscosity of the resulting latex increases with increasing molecular weight and decreasing hydrolysis of the PVA (318). 

Paine et al. [99] tried different stabilizers [i.e., hydroxy propylcellulose, poly(N-vinylpyrollidone), and poly(acrylic acid)] in the dispersion polymerization of styrene initiated with AIBN in the ethanol medium. The direct observation of the stained thin sections of the particles by transmission electron microscopy showed the existence of stabilizer layer in 10-20 nm thickness on the surface of the polystyrene particles. When the polystyrene latexes were dissolved in dioxane and precipitated with methanol, new latex particles with a similar surface stabilizer morphology were obtained. These results supported the grafting mechanism of stabilization during dispersion polymerization of styrene in polar solvents. 

Some research groups also tried to build up bi- and multilayers of latex particles by using self-assembly techniques [92-94,97]. Either the alternate adsorption technique outlined in Figure 14 was used, in which cationic and anionic particles are successively adsorbed, or a slightly modified version of successive adsorption of anionic particles and a cationic poly-... 

Figure 4b. Reaction of poly(vinylbenzyl chloride) latex with 0.35 M glycinate at 52.5°C. Diameter of latex particles 160 nm.

Polymeric particles can be constructed from a number of different monomers or copolymer combinations. Some of the more common ones include polystyrene (traditional latex particles), poly(styrene/divinylbenzene) copolymers, poly(styrene/acrylate) copolymers, polymethylmethacrylate (PMMA), poly(hydroxyethyl methacrylate) (pHEMA), poly(vinyltoluene), poly(styrene/butadiene) copolymers, and poly(styrene/vinyltoluene) copolymers. In addition, by mixing into the polymerization reaction combinations of functional monomers, one can create reactive or functional groups on the particle surface for subsequent coupling to affinity ligands. One example of this is a poly(styrene/acrylate) copolymer particle, which creates carboxylate groups within the polymer structure, the number of which is dependent on the ratio of monomers used in the polymerization process. 

Bagchi, P., and Birnbaum, S.M. (1981) Effect of pH on the adsorption of immunoglobulin G on anionic poly(vinyltoluene) model latex particles./. Colloid Interface Sci. 83, 460 178. 

An example of the effectiveness of this equation is given by an aqueous HEUR gel made up of a polymer with Mn = 20 x 103 Daltons at a concentration of 30kgm-3 filled with a poly(styrene) latex with a particle diameter of 0.2 pm at q> = 0.2. The unfilled gel had a network modulus of 0.4 kPa, whilst the modulus of the filled gel was 0.7 kPa. Equation (2.68) predicts a value of 0.728 kPa. The poly(styrene) particles act as a non-interactive filler because the surface is strongly hydrophobic as it consists mainly of benzene rings and adsorbs a monolayer of HEUR via the hydrophobic groups, resulting in a poly(ethylene oxide) coating that does not interact with the HEUR network. This latter point was... 

To illustrate how the effect of the adsorption on the modulus of the filled gel may be modelled we consider the interaction of the same HEUR polymer as described above but in this case filled with poly(ethylmetha-crylate) latex particles. In this case the particle surface is not so hydrophobic but adsorption of the poly (ethylene oxide) backbone is possible. Note that if a terminal hydrophobe of a chain is detached from a micellar cluster and is adsorbed onto the surface, there is no net change in the number of network links and hence the only change in modulus would be due to the volume fraction of the filler. It is only if the backbone is adsorbed that an increase in the number density of network links is produced. As the particles are relatively large compared to the chain dimensions, each adsorption site leads to one additional link. The situation is shown schematically in Figure 2.13. If the number density of additional network links is JVL, we may now write the relative modulus Gr — G/Gf as... 

Polyelectrolytes provide excellent stabilisation of colloidal dispersions when attached to particle surfaces as there is both a steric and electrostatic contribution, i.e. the particles are electrosterically stabilised. In addition the origin of the electrostatic interactions is displaced away from the particle surface and the origin of the van der Waals attraction, reinforcing the stability. Kaolinite stabilised by poly(acrylic acid) is a combination that would be typical of a paper-coating clay system. Acrylic acid or methacrylic acid is often copolymerised into the latex particles used in cement sytems giving particles which swell considerably in water. Figure 3.23 illustrates a viscosity curve for a copoly(styrene-... 

Other latexes which have been produced by this method include poly(butyl methacrylate), poly(butyl acrylate) and poly(styrene/DVB) [161]. Additionally, polymer blends were produced by mixing, under high shear, HIPEs of partially polymerised monomer, followed by completion of polymerisation. The conversion prior to blending had to be less than 5%, to allow efficient mixing of the highly viscous emulsions. The materials thus produced resembled agglomerates of latex particles, due to copolymerisation at the points of contact of partially polymerised droplets. 

Other nutshell materials have been synthesised [164]. Hydrophobic latex particles containing a crosslinked poly(VBC) core and a macroporous poly(styrene/DVB) shell were prepared from concentrated o/w emulsions. Similarly, hydrophilic porous particles of crosslinked acrylamide surrounding a linear poly(ethyleneoxide) core were formed from w/o HIPEs. The poly(VBC) cores of the hydrophobic particles were quaternised and used to bind [Co(CO)4] anions, whereas the hydrophilic latexes were employed in the immobilisation of lipase. 

Ahmed et al.t measured t]red/(i> for polystyrene latexes with adsorbed layers of commercial poly(vinyl alcohol) (PVA) samples of different molecular weights. The latex particles were 190 nm in diameter and the limiting values of as - 0 had the following values for PVA samples of the indicated molecular weight ... 

Garvey et al.85) made a similar sedimentation study on poly(vinyl alcohol) adsorbed on polystyrene latex particles. Adsorbance of the polymer was also measured. Both the thickness of the adsorbed layer and the adsorbance increased linearly with the square root of the molecular weight. The volume occupied by a polymer molecule in the adsorbed layer was approximately equal to that of the effective hydrodynamic sphere in bulk solution. However, the measured values of LH were greater than the hydrodynamic diameters of the polymer coils in solution. Thus, it may be concluded that adsorbed poly(vinyl alcohol) assumes a conformation elongated in the direction normal to the surface. 

Figure 16. Schematic of a latex particle with an adsorbed layer of poly electrolyte (- ) the extension in space of the adsorbed layer and (---------) the extension in...

Figure 10. Density of different polymer latex particles as a function of centrifugation time (N = 40.000 min 1) (Y ) polyvinyl acetate (%) poly(vinylacetate-co-ethylene) (A) polystyrene (X) poly( butadiene-co-styrene) (O) poly butadiene)...

Chang, K., Litt, M., and Jamieson, A. M., "The Measurement of Latex Particle Size by Quasielastic Laser Light Scatter-ing", J. Poly. Sci.-Phys., to be published. 

The transmission electron microscopy results are consistent with a segregated latex particle consisting of a polystyrene rich core and a soft poly-n-butyl acrylate rich shell. 

The latex particle diameter produced in the emulsion copolymerization of styrene with partially neutralized poly(methacrylic acid) macromonomers, 48, was studied as a function of degree of neutralization [127]. The latex particle... 

A. Loxley and B. Vincent, Equilibrium and kinetic aspects of the pH swelling of poly(vinylpyridine) latex particles, Colloid Polymer Sci. 275, 1108-1114 (1997). 

These applications require a good knowledge of the nature and magnitude of interactions between nucleic acids and polymer particles. To that purpose, many systematic studies were carried out by different authors and in this lab on the adsorption behavior of various nucleic acids onto various type latex microspheres, mostly cationic and anionically-charged polystyrene or hydrophilic (i.e. poly[N-isopropylacrylamide]) latex particles. 

Recently, core-shell type microgels, which contain a hydrophobic core and a hydrophilic thermosensitive shell, have become attractive for scientists because such systems can combine the properties characteristic of both the core and the shell [53], We have prepared core-shell microgel particles consisting of a poly(styrene) core onto which a shell of polyCA-isopropylacrylamide) (PS-PNIPA) has been affixed in a seeded emulsion polymerization [54-56], In this case, the ends of the crosslinked PNIPA chains are fixed to a solid core, which defines a solid boundary of the network. In this respect, these core-shell latex particles present crosslinked polymer brushes on defined spherical surfaces. The solvent quality can be changed from good solvent conditions at room temperature to poor solvent conditions at a temperature... 

Taniguchi T, Duracher D, Delair T, Elaissari A, Pichot C (2003) Adsorption/desorption behavior and covalent grafting of an antibody onto cationic amino-functionalized poly(styrene-/V-isopropyl aery I am i de) core-shell latex particles. Colloids Surf B Biointerfaces 29 53-65... 

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