PubMed · 5918734
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C G Hunter. 1966. Aromatic solvents.. https://doi.org/10.1093/annhyg%2F9.4.191
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Yield and selectivity of benzene produced from aquasonolysis of the selected cyclic C6Hx hydrocarbons, i.e., 1,4-cyclohexadiene, 1,3-cyclohexadiene, cyclohexene, cyclohexane, and methylcyclopentane, have been investigated in this work. Benzene cannot be detected during the aquasonolysis of cyclohexane and methylcyclopentane. The order of yield and selectivity of benzene was as follows: 1,4-cyclohexadiene>>1,3-cyclohexadiene>>cyclohexene. The initial concentrations of substrates can affect the yield of benzene. During the aquasonolysis of 1,3-cyclohexadiene and cyclohexene, other C6 species except benzene were also found. It was suggested that benzene could directly be generated by formal dehydrogenation of cyclic C6Hx hydrocarbons.
Soots were prepared from flame combustion of benzene and o-dichlorobenzene (ODCB), creating one soot without carbon-chlorine bonds (benzene soot) and one with such bonds (ODCB soot). ODCB soot was tested for PCDD/F formation between 277 and 600 degrees C without additional chlorine, but levels were very low. Copper and Cu2O were added as potential catalysts for ODCB soot oxidation, but levels of PCDD/F observed were even lower than without these additives. Both benzene soot and ODCB soot produced PCDD/F after adding CuCl2 to the reaction mixtures, suggesting that a (volatile) metal chloride was needed in order for PCDD/F formation to take place. Under the various conditions of [Cu2+], time, and temperature tested, ODCB soot was always more reactive than benzene soot in forming PCDD/F. It seemed plausible that, despite the fact that CuCl2 was very effective in creating C-Cl bonds in benzene soot, the C-Cl bonds created in ODCB soot during preparation were of a reactivity so as to make this soot especially prone to PCDD/F formation. High temperature (gas phase) chlorination of soots by HCI or other chlorinating agents, followed by deposition of these soots and condensed metal chlorides on the ducts and walls of the postcombustion zone, could create an effective mechanism for de novo formation of PCDD/F.
Frequency of intentional exposure to organic solvents has been increasing among children and adolescents in Brazil. Analysis of benzene, toluene and xylenes (BTX) in human blood is necessary to diagnose the intentional and accidental exposure to these solvents. A method for BTX determination in blood samples by gas chromatography preceded by solid phase microextration (SPME) from headspace (HS) has been described. SPME has several advantages when compared to other extraction techniques such as simplicity, low cost and solvent-free extraction. The method presents good repeatability (precision was of 2.2-8.0%), accuracy from -4.7 to -9.4%, limit of detection <1.0 ug/mL, linearity from 1.0 to 100 ug/mL for toluene and from 5.0 to 100 ug/mL for the other solvents (R2 > 0.99), which shows to be efficient and adequate for the detection of exposure to BTX in blood samples.