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Polyurea is a type of elastomer that is derived from the reaction product of an isocyanate component and an amine component. The isocyanate can be aromatic or aliphatic in nature. It can be monomer , polymer , or any variant reaction of isocyanates, quasi-prepolymer or a prepolymer .
The polyurethane urea elastomer (PUU), or poly (urethane urea) elastomer, is a flexible polymeric material that is composed of linkages made out of polyurethane and polyurea compounds. Due to its hyperelastic properties, it is capable of bouncing back high-speed ballistic projectiles as if the material had “hardened” upon impact.
Common interactions include hydrogen bonds, [32] metal coordination, ... In 2014 a polyurea elastomer-based material was shown to be self-healing, melding together ...
A roof coating is a monolithic, fully adhered, fluid applied roofing membrane. Many roof coatings are elastomeric, that is, they have elastic properties that allow them to stretch and return to their original shape without damage.
Moisture cure polyurethanes have been widely used in the adhesive and coating industries. Thermal, mechanical, and surface properties of hyperbranched polyurethane-urea (HBPU) moisture cured coatings have been studied in relationship to chemical structure. [3]
The kinetics and rates of step-growth polymerization can be described using a polyesterification mechanism. The simple esterification is an acid-catalyzed process in which protonation of the acid is followed by interaction with the alcohol to produce an ester and water. However, there are a few assumptions needed with this kinetic model.
[6] [7] Since then, the number of articles submitted per year on molecular layer deposition has increased steadily, and a more diverse range of deposited layers have been observed, including polyamides, [8] [9] [10] polyimines, [11] polyurea, [12] polythiourea [13] and some copolymers, [14] with special interest in the deposition of hybrid films.
To manufacture a polyaspartic ester, an amine is reacted with dialkyl maleate by the aza-Michael reaction. [8]Diethyl maleate is the usual maleate used. This converts the primary amines to secondary amines and also introduces bulky groups to the molecule which causes steric hindrance, slowing the reaction down.