Title page for ETD etd-04152004-074857

Document Type Doctoral Thesis
Author Labuschagne, Frederick Johannes Willem Jacobus
Email johanl@chamotte.co.za
URN etd-04152004-074857
Document Title Metal catalysed Intumescence of Polyhydroxyl compounds
Degree PhD(Chemical Engineering)
Department Chemical Engineering
Advisor Name Title
Prof WW Focke
  • latent base catalysed intumescence
  • metal catalysed intumescence
  • carbonisation
  • intumescent flame retardants
  • char
  • carbon foam
Date 2004-02-27
Availability unrestricted
Fire presents a great risk to humans and their possessions. Polymeric compounds are highly flammable and compounds are added to increase their fire resistance. These additives are referred to as flame retardants. Intumescent flame retardants are systems that form a carbon rich foam on the surface of the polymer during thermal degradation. A new field of metal catalysed intumescence is discussed in this document. The influence of both the metal ion and organic backbone of polyhydroxylcarboxylic acid metal salts was studied. The intumescence and foaming properties of selected salts were studied in more detail.

Gluconic acid proved to be the best intumescent and showed the best combination of carbon char yield, foam structure and volume, stability and open flame characteristics. As a general rule of thumb, the char volume and structure improved with an increased number of hydroxyl groups in the compound. Carbon char yield increased with an increase in the number of hydroxyl groups for a constant number of carbons in the complex. The number of acid groups in the compound played a lesser role in intumescence. Most metal complexes catalyse intumescent decomposition of polyhydric compounds such as polyhydroxylcarboxylic acids and pentaerythritol. The reduction in the volatilisation losses implies that the metal cations catalyse carbonisation reactions in the polyhydroxyl compound. Unfortunately, the resultant carbon-foams are unstable: the metal residues also catalyse the further oxidative degradation of the char. The low thermal stability of the compositions tested, as well as the afterglow effect makes them unsuitable for use as flame retardant additives in plastics. From the studies of the different metal complexes with acetylacetone and gluconic acid, it was concluded that the calcium ion exhibited the most promise.

When pyrolysed in air with an open gas flame or in a furnace, calcium gluconate monohydrate produces voluminous foam. The foam is of a closed cell structure, densely packed and has no mechanical strength. The cell walls are very thin (5 to 50 nm) and the cells are between 50 m and 200 m in size. If the sample is compressed before heating, the resultant foam produced during pyrolysis is less voluminous than that of the loose powder. The BET surface area of the calcium gluconate monohydrate foamed at 300C for 5 min. is 16.0 m2/g. The foam produced after 5 min heating at 300C has a thermal conductivity similar to standard polystyrene foam.

Adding leached silica to the calcium gluconate monohydrate increases mechanical strength of the foam, but influences the foam volume negatively. The optimum silica level was calculated to be 1:1 gluconate to silica on a mole ratio (11.8% SiO2 by mass). The mechanical strength of the foam can also be increased with the addition of expandable graphite. The graphite has a lesser influence on the foam volume than the silica, but also reduces the foam volume. However, the addition of the expandable graphite gives the sample more .opening. force, as the foam volume of a compressed sample pyrolysed, is similar to that of the heated loose powder.

Calcium gluconate monohydrate starts to degrade at 120C, losing its crystal water and shows a mass loss of 4% at 180C. The exothermic peak (shown in the DSC/TGA data) associated with the metal catalysed carbon oxidation (afterglow) is observed at 570C in air. For the calcium gluconate monohydrate the transition from CaCO3 to CaO occurs above 650C in air.

It has been shown that the foaming of polyhydroxylcarboxylic acids is due to the formation of water vapour during degradation. For calcium gluconate monohydrate, foaming starts due to the loss of crystal water and is continued by the loss of hydroxyl groups as water. The bulk of the foaming is due to the second reaction. It has been shown that compounds with crystal waters produce a more voluminous and lower density foam. The foam is an amorphous carbon rich residue. The molecular mass of the carbon residue increases up to a heating temperature of 300C. This implies that the carbon residue crosslinks during formation, forming a stretchable cell wall for the foam. Compounds with a .free. hydroxyl group at the end of the carbon chain produce a foam of larger volume and lower density. This supports the crosslinking theory. The foam produced when calcium gluconate monohydrate is heated for 5 min at 300C in air is of very low density . 2.5 kg/m3 based on residual mass.

The density of the calcium gluconate monohydrate pyrolysed at 1000C for 5 min in air yields a CaO with a density of 20 kg/m3 . This implies that the high temperature pyrolysis of calcium gluconate can produce an inorganic oxide of low bulk density and possible high specific surface area. The BET surface area of CaCO3 from the gluconate pyrolysed at 600C is ~ 12 m2 /g.

An intumescent coating containing calcium gluconate monohydrate, leached silica and expandable graphite as a system was prepared and compared to commercial formulations. This gluconate based system was at least as efficient as the commercial formulations when painted on balsa wood planks or aluminium plates. On cardboard sheets it did not perform as well as the commercial systems.

More work should be done to overcome the afterglow effect observed with metal- based intumescent systems. The crystal structure of calcium gluconate monohydrate should be determined as to understand the decomposition better. It is unclear whether the decomposition is catalysed inter- or intramolecularly.

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  00Front.pdf 256.26 Kb 00:01:11 00:00:36 00:00:32 00:00:16 00:00:01
  01Thesis.pdf 2.39 Mb 00:11:04 00:05:41 00:04:59 00:02:29 00:00:12
  02Appendices1.pdf 4.39 Mb 00:20:19 00:10:27 00:09:08 00:04:34 00:00:23
  03Appendices2.pdf 4.75 Mb 00:22:00 00:11:19 00:09:54 00:04:57 00:00:25

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