Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Linear polymers, emulsion polymerization

A research group in Lehigh University has extensively studied the synthesis and characterization of uniform macroporous styrene-divinylbenzene copolymer particles [125,126]. In their studies, uniform porous polymer particles were prepared via seeded emulsion polymerization in which linear polymer (polystyrene seed) or a mixture of linear polymer and solvent were used as inert diluents [125]. The average pore diameter was on the order of 1000 A with pore volumes up to... [Pg.221]

For example, the parameters g = 0.77, h = 0.94, p = 1.4, and C = 0.158 measured for a polymer sample and compared with the plots in Figures 7.11 through 7.13 were most consistent with athree-arm star monodisperse polymer a poly disperse three-arm star would have g= 1.12,/ = 1.05,p= 1.6, and C close to 0.2. °° The second example was poly(vinyl acetate) (PVAc) prepared by emulsion polymerization. Since no data for linear equivalent were available, g and h were not calculated. At lower conversion/MW p= 1.84 was found, only slightly higher than the theoretically expected p = 1.73 for a randomly branched architecture, p slightly decreased with increasing M, indicating... [Pg.209]

Perhaps the most common particle type used for bioapplications is the polymeric microsphere or nanosphere, which consists basically of a spherical, nonporous, hard particle made up of long, entwined linear or crosslinked polymers. Creation of these particles typically involves an emulsion polymerization process that uses vinyl monomers, sometimes in the presence of... [Pg.588]

Stage in —At an advanced stage of the polymerization (50 to 80% conversion), the supply of excess monomer becomes exhausted due to the disappearance of the monomer droplets. The polymer particles contain all the unreacted monomers. As the concentration of monomer in the polymer particles decreases, the rate of polymerization decreases steadily and deviates from linearity. The characteristics of various stages of emulsion polymerization are summarized in Table 10.4. [Pg.270]

Goetzinger, W., et al.. Characterization of high molecular mass linear polyacrylamide powder prepared by emulsion polymerization as a replaceable polymer matrix for DNA sequencing by capillary electrophoresis. Electrophoresis, 19, 242, 1998. [Pg.248]

Chem. Descrip. ium linear alkylbenzene sulfonate (22% sol n.) Uses Surfactant for emulsion polymerization of range of polymers incl. SBR, vinyl acetate, vinyl chloride, styrene and acrylic latexes defoamer in food-contact paper/paperboard in food-contact textiles in resinous/ polymeric food-contact coatings... [Pg.155]

Other types of IPN s exist, of course. For example, Johnson and Labana (1972) recently synthesized a modified type of latex IPN as follows A crosslinked polymer network I prepared by emulsion polymerization served as a seed latex to linear polymer II. The resulting semi-IPN exhibited the usual core-shell morphology. After suitable coagulation and molding steps, polymer II was selectively crosslinked to form a macroscopic network, resulting in a thermoset material. The topology of this IPN therefore involves microscopic network islands of polymer I embedded in a continuous network of polymer II. [Pg.268]

When the on-line measurement of the MWD or average molecular weight is not possible or not feasible, state estimationbecomes an alternative. The simplest state estimation scheme is the one that can be applied for linear polymers when CTAs are employed to control the MWD of the polymer. In these systems, the ratio of unreacted monomer to CTA provides an estimate of the instantaneous number chain length, DP = Rp/Rt = fcp[M]/fc [CTA]. Therefore, if the ratio can be measured on-line by one of the techniques described in the previous section, a good estimate of DP can be achieved. This feature has been used to monitor and control the MWD of linear homopolymer and copolymers produced in emulsion polymerization systems [104—107]. [Pg.329]

The polymer can be made by suspension, emulsion, solution, or bulk polymerization methods. Most of the PVC used in calendering, extrusion, and molding is prepared by suspension polymerization. Emulsion polymerized vinyl resins are used in plastisols and organisols. ° Only a small amount of commercial PVC is prepared by solution polymerization. The microstructure of PVC is mostly atactic, but a sufficient quantity of syndio-tactic portions of the chain allow for a low fraction of crystallinity (about 5 percent). The polymers are essentially linear, but a low number of short-chain branches may exist. The monomers are predominantly arranged head to tail along the backbone of the chain. Due to the presence of the chlorine group, PVC polymers are more polar than polyethylene. The molecular weights of commercial polymers are M = 100,000 to 200,000 ... [Pg.107]

Styrene butadiene n. A group of thermo plastic elastomers. They are linear co-polymers of styrene and butadiene, produced by lithium catalyzed solution polymerization, with a sandwich molecular structure containing a long Polybutadiene center surrounded by shorter polystyrene ends. A co-polymer of styrene and butadiene made by emulsion polymerization for use in latex paints. [Pg.937]

As pointed out by Hajji et al. [32], polymer blend nanocomposite systems can be prepared by various synthesis routes because of their ability to combine in different ways to introduce each phase. The organic component can be introduced as (1) a precursor, which can be a monomer or an oligomer (2) a preformed linear polymer (in molten, solution, or emulsion states) or (3) a polymer network, physically (eg, semicrystalline linear polymer) or chemically (eg, thermosets, elastomers) cross-linked. The mineral part can be introduced as (1) a precursor (eg, tetraethyl orthosilicate) or (2) preformed nanoparticles. Organic or inorganic polymerization generally becomes necessary if at least one of the starting moieties is a precursor. [Pg.8]


See other pages where Linear polymers, emulsion polymerization is mentioned: [Pg.497]    [Pg.93]    [Pg.147]    [Pg.194]    [Pg.663]    [Pg.245]    [Pg.205]    [Pg.529]    [Pg.199]    [Pg.16]    [Pg.114]    [Pg.487]    [Pg.67]    [Pg.497]    [Pg.320]    [Pg.325]    [Pg.342]    [Pg.264]    [Pg.608]    [Pg.580]    [Pg.497]    [Pg.271]    [Pg.60]    [Pg.524]    [Pg.150]    [Pg.197]    [Pg.77]    [Pg.194]    [Pg.60]    [Pg.84]    [Pg.30]    [Pg.302]    [Pg.313]    [Pg.314]    [Pg.3759]    [Pg.39]   


SEARCH



Emulsion polymerization

Emulsions, polymeric

Linear polymerizations

Polymerization emulsion polymerizations

Polymers emulsion

Polymers linearity

© 2024 chempedia.info