Latex density

Fig. XI-7. Volume fraction profile of 280,000-molecular-weight poly(ethylene oxide) adsorbed onto deuterated polystyrene latex at a surface density of 1.21 mg/m and suspended in D2O, from Ref. 70.

An interesting historical application of the Boltzmann equation involves examination of the number density of very small spherical globules of latex suspended in water. The particles are dishibuted in the potential gradient of the gravitational field. If an arbitrary point in the suspension is selected, the number of particles N at height h pm (1 pm= 10 m) above the reference point can be counted with a magnifying lens. In one series of measurements, the number of particles per unit volume of the suspension as a function of h was as shown in Table 3-3. 

The supporting medium was water at 298 K (p = 0.99727), and the density of latex is 1.2049 g cm . The latex particles had an average radius of 2.12 x 10 mm hence, their effective mass corrected for buoyancy is their volume times the density difference Ap between latex and the supporting medium, water... 

Latex mbber foams are generally prepared in slab or molded forms in the density range 64—128 kg/m (4—8 lbs/fT). Synthetic SBR latexes have replaced natural mbber latexes as the largest volume raw material for latex foam mbber. Other elastomers used in significant quantities are polychloroprene, nitrile mbbers, and synthetic i j -polyisoprene (115). 

Tensile Strength and Elongation. The tensile strength of latex mbber foam has been shown to depend on the density of the foam (149,177) and on the tensile strength of the parent mbber (177,178). At low densities the tensile modulus approximates a linear relation with density but kicreases with a higher power of density at higher densities. Similar relations hold for polyurethane and other flexible foams (156,179,180). 

The latex may consist entirely of natural latex or synthetic SBR latex or maybe a mixture of both. In the Dunlop process, natural mbber foams shrink more than SBR foams duriag washing and dryiag. The load-beariag capacity of the foams at a given density falls significantly as SBR is used ia place of natural mbber. 

Processing ndProperties. Neoprene has a variety of uses, both in latex and dry mbber form. The uses of the latex for dipping and coating have already been indicated. The dry mbber can be handled in the usual equipment, ie, mbber mills and Banbury mixers, to prepare various compounds. In addition to its excellent solvent resistance, polychloroprene is also much more resistant to oxidation or ozone attack than natural mbber. It is also more resistant to chemicals and has the additional property of flame resistance from the chlorine atoms. It exhibits good resiUence at room temperature, but has poor low temperature properties (crystallization). An interesting feature is its high density (1.23) resulting from the presence of chlorine in the chain this increases the price on a volume basis. 

Today polyether foam with a density of less than half that of rubber latex foam is widely used as a cushioning material. Polyester foams, although tending to be more expensive, continue to have a number of outlets, particularly where a high initial modulus is desirable. In addition to miscellaneous upholstery applications... 

If natural rubber is treated with proton donors a product is formed which has the same empirical formula. (CjHjj), and is soluble in hydrocarbon solvents but which has a higher density, is inelastic and whose unsaturation is only 51% that of natural rubber. It is believed that intramolecular ring formation occurs to give products containing the segments shown in Figure 30.5. Known as cyclised rubber it may be prepared by treating rubber, on a mill, in solvent or in a latex with materials such as sulphuric acid or stannic chloride. 

The Bingham plastic model can describe acrylic latex paint, with a yield stress of 112 dyn/cm2, a limiting viscosity of 80 cP, and a density of 0.95 g/cm3. What is the maximum thickness of this paint that can be applied to a vertical wall without running ... 

The adsorption of fully and partially hydrolyzed (88%) polyvinyl alcohol (PVA) on 190-1lOOnm monodisperse polystyrene latex particles was investigated. The effect of molecular weight was investigated for 190 nm-size particles using the serum replacement adsorption and desorption methods. The adsorption density at the adsorption-isotherm plateau followed the relationships for the fully hydrolyzed... 

PVA and TaM -for the 88%-hydrolyzed PVA. The same dependence was found for the adsorbed layer thickness measured by viscosity and photon correlation spectroscopy. Extension of the adsorption isotherms to higher concentrations gave a second rise in surface concentration, which was attributed to multilayer adsorption and incipient phase separation at the interface. The latex particle size had no effect on the adsorption density however, the thickness of the adsorbed layer increased with increasing particle size, which was attributed to changes in the configuration of the adsorbed polymer molecules. The electrolyte stability of the bare and PVA-covered particles showed that the bare particles coagulated in the primary minimum and the PVA-covered particles flocculated in the secondary minimum and the larger particles were less stable than the smaller particles. 

Polystyrene Latexes. The polystyrene latexes used were the mono-disperse LS-1102-A, LS-1103-A, and LS-1166-B (Dow Chemical Co.) with average particle diameters of 190, 400, and llOOnm, respectively. The latexes were cleaned by ion exchange with mixed Dcwex 50W-Dowex 1 resin (9). The double-distilled and deionized (DDI) water used had a conductivity of 4x10 ohm- cm-. The surface groups of the ion-exchanged latexes determined by conductometric titration (10) were strong-acid sulfates the surface charge densities were 1.35, 3.00 and 5.95 jiC/cm, respectively. 

Effect of PVA Molecular Weight on Adsorbed Layer Thickness. Figure 4 shows the variation of reduced viscosity with volume fraction for the bare and PVA-covered 190nm-size PS latex particles. For the bare particles, nre(j/ is independent of and the value of the Einstein coefficient is ca. 3.0. For the covered particles, rired/ t increases linearly with tp. Table IV gives the adsorbed layer thicknesses calculated from the differences in the intercepts for the bare and covered particles and determined by photon correlation spectroscopy, as well as the root-mean-square radii of gyration of the free polymer coil in solution. The agreement of the adsorbed layer thicknesses determined by two independent methods is remarkable. The increase in adsorbed layer thickness follows the same dependence on molecular weight as the adsorption density, i.e., for the fully hydrolyzed PVA s and... 

Polystyrene latices used as an adsorbent were prepared by the Kotera-Furusawa-Takeda method(8 to reduce the spurious effects of surface active substances. The average diameter(D) and the surface gharge density(ao) of the latex particles were determined D=2000 A and 0O = 1.5 uC/cm. A silica sample was prepared by the method described by Stttber et al.(9), and was composed of highly mono-disperse spherical particles of 1900 X in diameter. These colloids were used after dialyzing exhaustively against distilled water to remove the ionic impurities. 

Several experimental parameters have been used to describe the conformation of a polymer adsorbed at the solid-solution interface these include the thickness of the adsorbed layer (photon correlation spectroscopy(J ) (p.c.s.), small angle neutron scattering (2) (s.a.n.s.), ellipsometry (3) and force-distance measurements between adsorbed layers (A), and the surface bound fraction (e.s.r. (5), n.m.r. ( 6), calorimetry (7) and i.r. (8)). However, it is very difficult to describe the adsorbed layer with a single parameter and ideally the segment density profile of the adsorbed chain is required. Recently s.a.n.s. (9) has been used to obtain segment density profiles for polyethylene oxide (PEO) and partially hydrolysed polyvinyl alcohol adsorbed on polystyrene latex. For PEO, two types of system were examined one where the chains were terminally-anchored and the other where the polymer was physically adsorbed from solution. The profiles for these two... 

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