Reactivity Documentation
Polymerizable Compounds |
mixed with |
Polymerizable Compounds |
Summary
- Polymerization hazard: Polymerization reaction may become intense and may cause pressurization
- Potentially hazardous: May be hazardous but unknown
Details
Reactivity Predictions (for each pair of reactive groups)
Polymerizable Compounds
Hazard Predictions
- Polymerization hazard: Polymerization reaction may become intense and may cause pressurization
- Potentially hazardous: May be hazardous but unknown
In general most monomers, especially those of a similar nature such as acrylates, styrenics, etc. are compatible at ambient conditions. However, due to the complex inhibition mechanisms which may or may not involve dissolved oxygen, caution should be used when two monomers are mixed accidentally. Consequently, inadvertent mixtures need to be vetted carefully on an individual basis. Further research of comparable examples in the literature or very small scale, carefully controlled experiments may be needed to fully assess compatibility.
Polymerizable: Materials, commonly called monomers, that have the capability to undergo thermally induced or chemically initiated radical type polymerization reactions, which could generate significant amounts of heat (up to -100 kJ/mol) and pressure due to decomposition and formation of gas byproducts. These monomers are mainly the vinyl monomers common to the chemical industry such as styrene and its derivatives (including divinyl benzene), acrylamide and its derivatives, butadiene, acrylonitrile, vinyl acetate, and others. Also included here are the acrylates and acrylic acid derivatives but note that these materials are also captured in this tool in a separate and distinct category due to their unique hazards and their high volume of use in the industry.
These materials typically are inhibited with low ppm levels of antioxidants (inhibitors) to prevent premature polymerization chain reactions. Many of these inhibitors require dissolved oxygen to be effective. Inhibitor depletion is a function of time and temperature, with higher temperatures increasing depletion rates. These materials are known to be susceptible to destabilization due to low ppm levels of contaminants. Radical generating contaminants such as peroxides and azides are known to initiate monomer polymerization; however, the effects of seemingly benign materials are harder to predict. Therefore, extreme caution should be used in any contamination event. And the material should be presumed to be destabilized until testing and consultation with experts. Uncontrolled polymerization reactions can become adiabatic and lead to a serious runaway reaction with high temperatures and pressures. The general hazards of monomers are discussed in Frurip et al., Process Safety Progress (Vol. 14, No. 2) 1995.