Microwave driven trimethylsilylation of phenol-formaldehyde resins: Extent of reactions determined by 13C and 29Si n.m.r.

Parisa Monsef-Mirzai, Harminder Manak, William R. McWhinnie*, Colin E. Snape, Okin Sirkecioglu, John Andresen

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

A phenol-formaldehyde (PF) resite resin and phenol:2,6-di-t-butylphenol-formaldehyde (DTBPF) co-resite were reacted under conditions of microwave heating with N-(trimethylsilyl)imidazole (TMSI). Low degrees of reaction were observed for the PF resin (19%) and for the DTBPF co-resite (0.3-0.4%) as examples of macromolecular systems with very limited porosity. 13C SPE MAS n.m.r. was an effective method to determine the degree of silylation and 13C CP MAS n.m.r. gave very similar results. When a different reagent mix (1:1:1 N,O-bis(trimethylsilyl)acetamide:N(trimethylsilyl)imidazole: trimethylchlorosilane) was used both 13C and 29Si SPE n.m.r. were in agreement that 100% silylation of the OH groups had been achieved for the PF resin. Thus, with proper choice of conditions and reagents, microwave-driven silylation is a very effective method of OH analysis even for systems of significantly more limited porosity compared with coals.

Original languageEnglish
Pages (from-to)369-374
Number of pages6
JournalFuel
Volume77
Issue number5
DOIs
Publication statusPublished - Apr 1998
Externally publishedYes

Keywords

  • MAS n.m.r.
  • Microwave heating
  • Phenol-formaldehyde resites
  • Silylation

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