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PubMed1978

Ingested mutagens from opium and tobacco pyrolysis products and cancer of the oesophagus.

Substances which are commonly sucked or chewed in two areas where the incidence of oesophageal cancer is high, the Transkei and north-east Iran, were tested in bacterial mutagenicity assays. Pyrolysed substances, opium dross in north-east Iran and tobacco pipe residues in the Transkei, displayed mutagenic activity in Salmonella typhimurium strains TA98 and TA100 in the presence of rat liver microsomes.

Administration, Oral↗
PubMed2001

Carbon and char residue yields from rapid pyrolysis of kraft black liquor.

The yields of char residue, fixed carbon, and inorganic carbonate were measured for oxidized black liquor char residues produced in a laboratory laminar entrained-flow reactor (LEFR) at heating rates of 4000-13,000 degrees C/s. The char residue yields at the end of devolatilization thus obtained decreased nearly linearly with temperature, from 75% at 700 degrees C to 58% at 1100 degrees C. There were explainable differences in the char residue yields from the liquor used in this study and those used in other studies. Char residue yields seemed to depend mainly on the temperature to which the particles or droplets were exposed and were not very sensitive to heating rate. Fixed carbon yields behaved similarly to those of the char residue. The fixed carbon remaining at the end of devolatilization decreased from 67% at 700 degrees C to about 45% at 1100 degrees C. The carbonate content in black liquor changed very little before and after devolatilization.

Carbon↗
PubMed2003

GC/MS determination of fatty acid picolinyl esters by direct curie-point pyrolysis of whole bacterial cells.

A single-step method suitable for cellular fatty acid derivatization to picolinyl esters with the use of a pyrolyzer as a thermochemical micro-reactor was developed for whole bacterial cells. This reduced the preparation time from several hours to less than two minutes. In addition, the minimal bacterial mass required for analysis was reduced from several milligrams to micrograms. The profiling of cellular fatty acids of gram-positive and gram-negative bacteria was achieved using three derivatization methods: preparation of methyl esters, beta-picolinyl esters by Harvey's method and a new method based on pyrolytic derivatization to beta-picolinyl esters. It was shown that there are great similarities between profiles of bacterial fatty acids determined by the pyrolytic derivatization method and traditional preparation methods of picolinyl and methyl esters prior to GC analysis. Results obtained by application of the new technique have immense diagnostic value due to vast similarities between profiles of fatty acids derivatized to either picolinyl and methyl esters. Although the latter are referred to in the literature most often, mass spectra of picolinyl esters contain fragment ions that provide structural information about the chain branching, position of unsaturation, and other substituents.

Bacteria↗
PubMed2000

Ultrasound-induced cracking and pyrolysis of some aromatic and naphthenic hydrocarbons.

The action of intense ultrasound on solutions of decahydronaphthalene (decalin) or tetrahydronaphthalene (tetralin) causes, in both cases, a dehydrogenation reaction at room temperature. According to thermodynamic calculations, temperatures as high as 500 degrees C are necessary to achieve the same results. The use of Pd and Se as dehydrogenation catalysts has confirmed the dehydrogenation reactions. Benzene and toluene sonication at room temperature causes aromatic ring breakdown with formation of acetylene and other products. The analogy with radiolysis was noticed. A thermodynamic analysis was conducted on the possible reaction products formed from benzene ring cleavage including polymerization products. It was concluded that acetylene formation from benzene is possible for instance at 650 degrees C only if it is accompanied by coke formation. Otherwise temperatures as high as 1700 degrees C are needed. The nature of the 'coke' formed during sonication is discussed, it was revealed by FT-IR spectroscopy to be a crosslinked polystyrene and hence it is a sonopolymer derived from benzene or toluene ring breakdown products reacted with phenyl and polyphenyl radicals. Again the striking analogy between the IR spectrum of irradiated polystyrene and benzene sonopolymer was noticed. The formation of poly-p-phenylene was excluded by the FT-IR pattern which did not match that of an authentic sample.

Journal Article↗