0000000000324074
AUTHOR
Raili Vesterinen
showing 3 related works from this author
Chlorinated dioxins and dibenzothiophenes in fly ash samples from combustion of peat, wood chips, refuse derived fuels and liquid packaging boards
1995
Abstract Peat, wood chips, refuse derived fuel and liquid packaging board in different combinations were burned at a temperature of at least 850 °C. Fly ash samples from these combustions were analyzed for polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzothiophenes (PCDBTs) by high resolution GC/MS. The concentrations of tri- and tetrachlorodibenzothiophenes and tri-, tetra- and pentachlorodioxins were highest when mixtures of wood chips and refuse derived fuel (RDF) were burned. The fly ash from the combustion of pure peat pellets did not contain any polychlorinated dibenzothiophenes. When wood chips and RDF were burned the concentrations of chlorinated compounds in fly…
Three nuclei n.m.r. spectroscopy of dimethoate compounds. A large solvent effect on the31PSC1H vicinal coupling
1977
Proton, phosphorus and carbon magnetic resonance spectra of dimethoate, dimethoxon, des-N-methyldimethoate, ω-hydroxydimethoate, trimethyldithiophosphate and O,O-dimethyldithiophosphate in different solvents have been measured. Most of the n.m.r. parameters were characteristic of the structural environment of the corresponding nucleus and solvent-independent. However, in the amide structures dimethoate, dimethoxon, des-N-methyldimethoate and ω-hydroxydimethoate the 31PSC1H vicinal coupling showed an unusually large solvent effect of a 2.3 to 6.5 Hz decrease when CDCI3 was replaced by acetone-d6 or DMSO-d6.
The decomposition of 1-phenyl-3-chloro-nortricyclene and 1-phenylnortricyclene on reduction in 1,2-dimethoxyethane. The EPR spectra of the radical io…
1972
Radical anions of 1-phenyl-3-chloronortricyclene and 1-phenylnortricyclene were produced by reduction with potassium in 1,2-dimethoxyethane under a high vacuum. The initially formed radical anion of 1-phenyl-3-chloronortricyclene was very unstable, and decomposed finally to the anions of naphthalene and biphenyl. The only product of the reduction of 1-phenylnortricyclene was the biphenyl anion. The EPR spectra of the reaction mixtures were measured at temperatures from —80°C to room temperature.