Peptization

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Peptization or deflocculation is the process of converting precipitate into colloid by shaking it with a suitable electrolyte called peptizing agent.

This is particularly important in colloid chemistry or for precipitation reactions in an aqueous solution. When colloidal particles bear a same sign electric charge, they mutually repel each other and cannot aggregate together. Freshly precipitated aluminium or iron hydroxide is extremely difficult to filter because the very fine colloidal particles directly pass through a paper filter. To facilitate the filtration, the colloidal suspension must be first flocculated by adding a concentrated solution of salt to the system. Multivalent cations are more efficient flocculants than monovalent cations: AlCl3 > CaCl2 > NaCl. The electrical charges present at the surface of the particles are so "neutralised" and disappear. More correctly speaking, the electrical double layer existing at the surface of the particles is compressed by the added electrolyte and collapses at high ionic strength. The electrical repulsion no longer hinders the aggregation of particles and they can then coalesce to form a flocculent precipitate that is easy to filter. If the precipitate is washed with an excessive volume of deionised water, the electrical double layer present at the surface of the particles expands again and the electrical repulsion reappears: the precipitate peptizes and the particles pass again through the filter.

Peptization is also used in nanoparticle synthesis to make a large grouping of particles split into many primary particles. This is done by changing the surface properties, applying a charge, or by adding a surfactant.

In the synthesis of titania (titanium dioxide) nanoparticles, peptization involves adsorption of quaternary ammonium cation on the titania surface. This causes the surface to become positively charged. Electrostatic repulsion of the primary particles in the agglomerated titania breaks up the agglomerate into primary particles. [1] The efficacy of adsorbates or suspension modification in imparting interparticle electrostatic repulsion is most commonly studied in terms of zeta potential.

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Suspension (chemistry) Heterogeneous mixture of solid particles dispersed in a medium

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Gravimetric analysis Quantitative determination of a chemical species based on its mass

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Zeta potential Electrokinetic potential in colloidal dispersions

Zeta potential is the electrical potential at the slipping plane. This plane is the interface which separates mobile fluid from fluid that remains attached to the surface.

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Polyelectrolyte Polymers whose repeating units bear an electrolyte group

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Flocculation Process by which colloidal particles come out of suspension to precipitate as floc or flake

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Particle aggregation

Particle agglomeration refers to formation of assemblages in a suspension and represents a mechanism leading to the functional destabilization of colloidal systems. During this process, particles dispersed in the liquid phase stick to each other, and spontaneously form irregular particle assemblages, flocs, or agglomerates. This phenomenon is also referred to as coagulation or flocculation and such a suspension is also called unstable. Particle agglomeration can be induced by adding salts or other chemicals referred to as coagulant or flocculant.

Double layer (surface science) Condensed matter physics

A double layer is a structure that appears on the surface of an object when it is exposed to a fluid. The object might be a solid particle, a gas bubble, a liquid droplet, or a porous body. The DL refers to two parallel layers of charge surrounding the object. The first layer, the surface charge, consists of ions adsorbed onto the object due to chemical interactions. The second layer is composed of ions attracted to the surface charge via the Coulomb force, electrically screening the first layer. This second layer is loosely associated with the object. It is made of free ions that move in the fluid under the influence of electric attraction and thermal motion rather than being firmly anchored. It is thus called the "diffuse layer".

Sedimentation potential occurs when dispersed particles move under the influence of either gravity or centrifugation in a medium. This motion disrupts the equilibrium symmetry of the particle's double layer. While the particle moves, the ions in the electric double layer lag behind due to the liquid flow. This causes a slight displacement between the surface charge and the electric charge of the diffuse layer. As a result, the moving particle creates a dipole moment. The sum of all of the dipoles generates an electric field which is called sedimentation potential. It can be measured with an open electrical circuit, which is also called sedimentation current.

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Particle deposition

Particle deposition is the spontaneous attachment of particles to surfaces. The particles in question are normally colloidal particles, while the surfaces involved may be planar, curved, or may represent particles much larger in size than the depositing ones. Deposition processes may be triggered by appropriate hydrodynamic flow conditions and favorable particle-surface interactions. Depositing particles may just form a monolayer which further inhibits additional particle deposition, and thereby one refers to surface blocking. Initially attached particles may also serve as seeds for further particle deposition, which leads to the formation of thicker particle deposits, and this process is termed as surface ripening or fouling. While deposition processes are normally irreversible, initially deposited particles may also detach. The latter process is known as particle release and is often triggered by the addition of appropriate chemicals or a modification in flow conditions.

Polyelectrolytes are charged polymers capable of stabilizing colloidal emulsions through electrostatic interactions. Their effectiveness can be dependent on molecular weight, pH, solvent polarity, ionic strength, and the hydrophilic-lipophilic balance (HLB). Stabilized emulsions are useful in many industrial processes, including deflocculation, drug delivery, petroleum waste treatment, and food technology.

Double layer forces

Double layer forces occur between charged objects across liquids, typically water. This force acts over distances that are comparable to the Debye length, which is on the order of one to a few tenths of nanometers. The strength of these forces increases with the magnitude of the surface charge density. For two similarly charged objects, this force is repulsive and decays exponentially at larger distances, see figure. For unequally charged objects and eventually at shorted distances, these forces may also be attractive. The theory due to Derjaguin, Landau, Verwey, and Overbeek (DLVO) combines such double layer forces together with Van der Waals forces in order to estimate the actual interaction potential between colloidal particles.

Dispersion Technology Inc is a scientific instrument manufacturer located in Bedford Hills, New York. It was founded in 1996 by Philip Goetz and Dr. Andrei Dukhin. The company develops and sells analytical instruments intended for characterizing concentrated dispersions and emulsions, complying with the International Standards for acoustic particle sizing ISO 20998 and Electroacoustic zeta potential measurement ISO 13099.

In 2015, 251 million tubes of toothpaste were sold in the United States. A single tube holds roughly 170 grams of toothpaste, so approximately 43 kilotonnes of toothpaste get washed into the water systems annually. Toothpaste contains silver nanoparticles, also known as nanosilver or AgNPs, among other compounds.

References

  1. Y. Li, T. J. White; Lim, S. H.; Lim, S.H (2004). "Low-temperature synthesis and microstructural control of titania nano-particles". Journal of Solid State Chemistry. 177 (4–5): 1372–1381. Bibcode:2004JSSCh.177.1372L. doi:10.1016/j.jssc.2003.11.016.