28.02.2013 Views

Handbook of Solvents - George Wypych - ChemTech - Ventech!

Handbook of Solvents - George Wypych - ChemTech - Ventech!

Handbook of Solvents - George Wypych - ChemTech - Ventech!

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

972 David Randall<br />

Hydrophobic substances such as hydrocarbons will prefer to be within the polymer<br />

particle; these are described as A Group coalescents. These tend to be inefficient coalescing<br />

agents. Molecules, which are more hydrophilic than hydrocarbons tend to be preferentially<br />

sited at the particle - aqueous interface, along with the surfactant system. These are described<br />

as AB Group coalescents. These exhibit the best efficiency as coalescing solvents.<br />

In the third group are the hydrophobic glycol ethers and similar species. These exhibit<br />

good coalescing power, but are partitioned between the polymer particle, the boundary<br />

layer, and the aqueous phase. More <strong>of</strong> these are required than AB Group coalescents, they<br />

are called ABC Group coalescents. Finally, hydrophilic species such as glycols and the<br />

more polar glycol ethers are inefficient coalescing agents, and are more commonly used as<br />

freeze thaw stabilizers. These are described as C Group coalescents.<br />

14.19.2.5 Properties <strong>of</strong> coalescing agents<br />

14.19.2.5.1 Hydrolytic stability<br />

A coalescing agent should have good hydrolytic stability (a high degree <strong>of</strong> resistance to hydrolysis)<br />

so that it can be used successfully in both low and high pH latex systems.<br />

14.19.2.5.2 Water solubility<br />

It is desirable for a coalescing aid to have low water miscibility for the following reasons:<br />

• When added to a coating formulation, a coalescing aid with low water miscibility<br />

partitions into the polymer phase and s<strong>of</strong>tens the polymer; this improves pigment<br />

binding and polymer fusion.<br />

• There is less tendency for the evaporation <strong>of</strong> the coalescing aid to be accelerated by<br />

evaporation <strong>of</strong> the water during the early stages <strong>of</strong> drying.<br />

• The early water resistance <strong>of</strong> the coating is not adversely affected.<br />

• When a latex coating is applied to a porous substrate, water immiscible coalescing<br />

aids are not lost into the porous substrate along with the water; i.e., more coalescing<br />

aid will be available to coalesce the coating.<br />

14.19.2.5.3 Freezing point<br />

The freezing point <strong>of</strong> a coalescing agent should be low (below -20°C) as materials with a<br />

high freezing point may require specialized (therefore more expensive) handling techniques<br />

in transport and storage.<br />

14.19.2.5.4 Evaporation rate<br />

The evaporation rate <strong>of</strong> a coalescing aid should be slow enough to ensure good film formation<br />

<strong>of</strong> the emulsion coating under a wide range <strong>of</strong> humidity and temperature conditions;<br />

however, it should be fast enough to leave the coating<br />

film in a reasonable length <strong>of</strong> time and not cause<br />

excessive film s<strong>of</strong>tness. The evaporation rate <strong>of</strong> the<br />

coalescing aid should be less than that <strong>of</strong> water but<br />

not so slow that it remains in the film for an extended<br />

period <strong>of</strong> time causing dirt pickup.<br />

14.19.2.5.5 Odor<br />

Figure 14.19.2.5. Location <strong>of</strong> species in aqueous<br />

dispersions.<br />

The odor <strong>of</strong> a coalescing agent should be minimal.<br />

This is especially important for interior coatings applications.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!