PubMed · 13575376
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H KOLDER. 1958. Explosive recompression.. https://pubmed.ncbi.nlm.nih.gov/13575376/
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The miniaturized mass-spectrometric detector with atmospheric pressure chemical ionization (APCI) is described. The analyzer employed in this instrument is the monopole with rod 54 mm in length and 2 mm in radius, which retains its efficiency up to 0.13 Pa ( approximately 10(-3)Torr). Together with the ion source, channeltron ion detector, radio frequency power supply and preamplifier, it is packed into a case with dimension of 185 mm x 100 mm x 70 mm. Mass spectrometer with the whole vacuum system weighs about 20 kg. In spite of low power of the vacuum system, the limit of detection at ppt level is achieved. The "strong" fragmentation mode is suggested for high-specific detection of phosphor-containing substances. The detector conforms to multicapillary column attachment.
Denitrification using methane as sole electron donor under anoxic condition was investigated. Sludge produced by a denitrifying reactor using acetate as electron donor was put in contact with methane at partial pressures from 1.8 to 35.7kPa. Nitrate depletion and gaseous nitrogen production were measured. The denitrification rate was independent of the methane partial pressure when superior or equal to 8.8kPa. The nitrate depletion was asymptotic. A denitrification rate of 0.25g NO(3)(-)-Ng(-1) VSSd(-1) was observed at the onset of culturing, followed by a slower and lineal denitrification rate of 4.9x10(-3)g NO(3)(-)-Ng(-1) VSSd(-1). Abiotic nitrate removal or the availability of another carbon source were discarded from control experiments made in the absence of methane or using sterilized inoculum.
An analytical method for the determination of residues of the antibiotic drugs lincomycin and tylosin in honey was developed. The procedure employed a solid-phase extraction for the isolation of lincomycin and tylosin from diluted honey samples. The antibiotic residues were subsequently analyzed by reversed-phase HPLC with atmospheric pressure chemical ionization mass spectrometric detection. Average analyte recoveries for lincomycin and tylosin ranged from 84 to 107% in replicate sets of honey samples fortified with drug concentrations of 0.01, 0.5, and 10 microg/g. The method detection limits were determined to be 0.007 and 0.01 microg/g for lincomycin and tylosin, respectively.