Antifoams and Defoamers



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Your One-Stop Source to learn about Antifoams, their properties, how Defoamers work, and the breakdown of unwanted foaming.

 


Mechanism

Foam formation is the result of dissolved molecules in a liquid. The dissolved molecules alter the surface tension of the liquid, and can be viewed as surface active agents (surfactants). The surfactants can be nonionic, cationic, anionic, or amphoteric. The liquid can be either aqueous, nonaqueous, or both (some industrial systems may contain dissolved organics which require special consideration). Different surfactants will generate different types of foam, and foam stability. When agitated, bubbles will form, which will immediately encounter gravitational effects pulling liquid along the bubble walls back down into the liquid beneath the bubble. A simplified picture of a bubble can be described as spherical, having both an outer wall and inner wall.

Nonionic surfactant generated foam is generally depicted as having a hydrophobic head (water insoluble portion) at the air-liquid interface, and the hydrophilic tail (water soluble portion) at an aqueous solution. Its orientation would be reversed in nonaqueous liquids.

Anionic surfactant generated foam would have a negative charge on the hydrophilic tail. As aqueous liquid is pulled down over the bubble's surface, the negative charges reach a concentration at the bubble at the liquid interface. Most often the negative charge serves to stabilize the bubble, and will begin to repel each other at the interface. This phenomenon is known as an electrostatic repulsion.

Cationic surfactant generated foam would have a positive charge on the hydrophilic tail, and would exhibit similar behavior as the anionic surfactant in an ideal aqueous liquid.

When the surface tension is high enough, bubble formation becomes more rigid and stable. If a bubble is subjected to mechanical agitation, bubbles caused by entrained air, would form very stable lamellar structures. The Marangoni effect is a major stabilizing factor in foam, and is driven by osmotic pressure. In some cases, the aqueous liquid is being pulled through the bubbles' walls creating regions of low and high surfactant concentrations, which sets up a gradient along the bubbles' surface. The gradient would pump liquid back onto the bubble walls, where this phenomenon is referred to as a surface transport.

The bulk viscosity also contributed to foam stability. As the viscosity of liquids increase, entrained air, now a bubble, can be trapped below the liquid's surface. Increasing viscosity of the system also reduces the coalescence capability of smaller bubbles merging to become larger bubbles. If the bubbles become large enough (increasing the diameter), bubble stability decreases. The surface viscosity is also important, as it effects the coalescence formation between bubbles. The higher the bulk viscosity becomes, the lower the coalescence formation is between bubbles.

When the surface tension is lowered on the bubble, it will burst. The resulting interaction of the defoamer to disperse the foam and its bubble formation is a physical interaction with the aqueous liquid. We engineer defoamers to work with specific applications and their systems. We use a check list to describe the criteria in which form is generated and from this check list, a defoamer selection is made to begin testing.

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Last updated January, 2007
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