A process was developed for the microencapsulation of inorganic filler part
icles with poly-methyl-methacrylate, to increase the interaction between th
e hydrophilic filler particles and a polymer matrix. The filler utilised wa
s aluminium hydroxide with an average diameter of 1.9 mum and a specific su
rface area of 5 m(2)/g. The process comprised a surface modification, in wh
ich a monolayer of isopropoxy titanium isostearate was chemically bound to
the surface to render it hydrophobic and to ensure a chemical bond between
the filler and the organic phase. Then, an encapsulation reaction was carri
ed out by means of an emulsion-like polymerization process at monomer starv
ed conditions. The modified particles were stabilized in water with sodium-
dodecyl-sulphate. A redox system consisting of cumene-hydroperoxide in comb
ination with sodium-formaldehyde-sulphoxylate and iron(II) salt was applied
for the initiation of the polymerization. Besides surface polymer, free po
lymer particles were also formed. The parameters which varied were the fill
er concentration, the concentration of the initiator components and the sur
factant concentration. At optimum conditions, similar to 50% of the added m
onomer polymerized at the modified filler surface, thus forming encapsulate
d filler particles. SEM together with TGA analysis indicated that a smooth
polymer layer had been formed on the filler surface. At high filler loading
, however, coagulation occurred.