Polyester polyols are an important group of raw materials used in polyurethane chemistry, determining the structure, reactivity and properties of the final PUR materials. Their structure, based on ester bonds and reactive hydroxyl groups, allows for the precise design of elastomers, foams, coatings and CASE systems with diverse mechanical and chemical parameters.
The structure of polyester polyols is characterised by the presence of numerous ester bonds (–COO–) and active hydroxyl groups, which react with isocyanates to form urethane bonds (–NH–CO–O–), which form the basis of the polyurethane structure.
They are obtained from aliphatic dicarboxylic acids and glycols and are characterised by good flexibility and resistance to hydrolysis. Due to their structure, they exhibit better UV stability and a lower tendency to yellowing, which makes them suitable for applications requiring colour fastness.
Aromatic polyester polyols contain aromatic rings in their structure, most often derived from phthalic or terephthalic acid, which translates into high rigidity and thermal resistance of the final materials. They are widely used where mechanical strength and chemical resistance are key.
The manufacturing process involves combining diols and acids, e.g. glycols with adipic acid or other di-,tricarboxylic reagents, under elevated temperature conditions, often with the removal of water formed in the reaction, which leads to the elongation of the polyester chain and the obtaining of a polyol with a specified hydroxyl character and functionality.
A significant difference from polyether polyols is the presence of ester bonds in the backbone. Polyester polyols contain primary hydroxyl groups, which makes them less reactive but also more resistant to hydrolysis. Ester segments can improve adhesion and resistance to solvents and chemicals compared to their polyether counterparts.
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