Particle colloidally stable

Surfactant keeps emulsion droplets and latex particles colloidally stable against coalescence/aggregation. The surfactant plays another important role in emulsion polymerisation besides stabilisation. Surfactant is critically involved in the nucleation mechanism (i.e., how the particles are formed) of the polymer latex particles (418,419). The amount of surfactant used is critical in controlling the latex particle size distribution. As surfactant is added to an emulsion, some remains dissolved in the aqueous phase, and some adsorbs onto the surface of the emulsion droplets according to an adsorption isotherm (e.g., Langmuir, Freundhch, or Frumkin adsorption isotherms) (173). 

Taken together, the experimental observations reported in the previous sections suggest that the formation of colloidally stable particles heated above their phase-transition temperature may be a universal phenomenon, taking place not only in aqueous polymer solutions, but also in solutions of polymers that can undergo a coil-globule transition in organic solvents. 

Under what conditions are colloids stable Explain qualitatively (with schematic diagrams) the forces between colloidal particles. How does the force of repulsion between them vary with concentration As the concentration of the colloid increases, there is the tendency to coagulate and in fact the critical concentration for coagulation gets less as the valence of the ions present increases (Schulze-Hardy rule). Give a detailed, although qualitative, rationalization of this law. (Bockris)... 

More generally, it is widely recognized that it is the establishment of repulsive electrostatic forces stronger than attractive van der Waals forces that is the main effective mechanism preventing aggregation of biopolymer molecules and colloidal particles in stable aqueous systems. 

Colloids are always present in natural waters containing the transuranium elements. (Colloids are defined as particles with sizes ranging from 1 to 450 nm. These particles form stable suspensions in natural waters.) Colloids of the transuranium elements can be formed by hydrolysis of transuranium ions, or by the sorption of transuranium elements on the naturally occurring colloids. The naturally occurring colloids include such species as metal hydroxides, silicate polymers, organics (such as humates), and the like. The mobility of the transuranium elements in an aquifer is determined largely by the mobility of its pseudocolloids, that is, those colloidal species formed by the adsorption of the transuranium ions upon the naturally occurring colloids. 

The colloidal stable polymer dispersions, the monodisperse polymer particles, and high conversions (85-100%) can be obtained with most of the other macromonomers (MAL,VB, and MA) of PEO (MW>PEO=2000)) [76]. Also, when macromonomers are used (3.1 wt% based on styrene), there is practically no coagulum produced. This is not the case in the presence of polymerizable PEO surfactants (surfmer I R1=CH3(CH2)11-, R2=H, n=34 and surfmer II R =CH3 (CH2)n-, R2=H, n=42) despite the higher amounts of stabilizer used (up to 60 wt% of coagulum). Furthermore, the particles are more monodisperse with PEO macromonomer (Dw/Dn=1.025 for PEO-MA and 1.13 for PVPo) compared to those with surfmer. Comparatively poorer results were obtained with conventional surfactants such as ethoxylated nonylphenol, even when used in large amounts. 

In later stages of the polymerization it is possible to have a situation in which the larger particles bear enough charges to be colloidally stable, but where N r is not large enough to prevent nucleation. A steady state may soon be reached in which dN/dt = 0. Then, according to Equation 3,... 

The chemistry and physics of such particles represent a separate, rapidly developing field. The consideration of this field (even if brief) is beyond the scope of this review. From the standpoint of this review, of most interest is the fact that melting of similar films often produces stable colloid solutions of metals in non-aqueous media. Early works in this field were summarized in review [19]. Among later results, noteworthy is the stabilization of metal nanoparticles in tertiary amines, which appear to be a unique medium for formation of stable colloid solutions of a wide variety of metals [20, 21]. Metal colloids stable for, at least, several years were obtained through the intermediate formation of thin films of co-condensates of metals with amines. 

When either ion-hydration interaction or ion-dispersion forces were included in the treatment, the results were qualitatively identical to the traditional DLVO theory, which roughly predicts that strongly charged colloidal particles are stable, and weakly charged particles coagulate. Significant quantitative differences, which can account for specific ion effects, could he introduced by either mechanism, when suitable interaction parameters were selected. 

Colloids Stable mixtures in which particles of rather large sizes (ranging from 1 nm to 1 tm) are dispersed throughout another substance. 

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