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The relationship between mutagenicity and chemical composition of polycyclic aromatic compounds from coal pyrolysis.

The polycyclic aromatic compounds (PAC) produced from the pyrolysis of a bituminous coal at temperatures of 1125 to 1425 degrees K prove to be mutagenic to S. typhimurium, both in the presence and in the absence of postmitochondrial supernatant (PMS) prepared from Aroclor 1254-induced rat liver. Mutagenicity of the PAC samples measured in the absence of PMS exhibits little dependence on pyrolysis temperature; that measured in its presence is higher at the higher pyrolysis temperatures. However, because of the decrease in PAC yield as the temperature is raised, mutagenicity per mass of coal consumed falls with an increase in temperature if measured without PMS (-PMS) and peaks at an intermediate temperature of 1378 degrees K if measured with PMS (+PMS). Using a new chromatographic technique, we have split each coal-derived PAC sample into two fractions: LC1, containing PAC with alkyl and O-containing substitutions and LC2, consisting of unsubstituted PAC. Substituted (LC1) fractions show no significant +PMS mutagenicity, indicating that, as a whole, the alkylated PAC in our coal pyrolysis products are not mutagenic. Only at the higher temperatures do the substituted fractions exhibit significant -PMS mutagenicity, attributed to PAC with carbonyl or etheric functionalities. The extremely low yields of the substituted PAC under the conditions where they show some activity, however, ensure that they contribute little to overall mutagenicity. In contrast to the substituted fractions, the unsubstituted (LC2) fractions display significant mutagenicity under all conditions and appear to be responsible for virtually all of the mutagenicity in these coal-derived PAC samples. In this fraction, -PMS activity is attributed to nitrogen-containing heterocyclic aromatics.

Animals↗

Optical and mass spectrometric study of the pyrolysis gas of wood particles.

A detailed experimental investigation has been made of the pyrolysis--the first step in biomass combustion--of single birchwood particles. In addition to mass spectrometric and gravimetric analysis, the pyrolysis volatiles were characterized by different optical techniques. Absorption measurements showed a nearly featureless absorption in the ultraviolet spectral region with a continuously stronger absorption for shorter wavelengths. Using different excitation wavelengths, laser-induced fluorescence measurements revealed generally broad spectra in the spectral region from 300-500 nm, which are characteristic spectral signatures for larger hydrocarbons. The optical data were monitored at different times in the pyrolysis process of the particles and compared with the results from the mass spectrometric and gravimetric analysis. The sensitivity of the optical techniques for differentiation between specific molecules was rather low, although formaldehyde could be observed both in absorption and fluorescence spectra. Laser-induced fluorescence measurements were also made for two-dimensional visualization of the pyrolysis volatiles emitted from heated birchwood particles, indicating much higher flows along the fiber direction than across.

Anisotropy↗

[Differences in the mechanisms of low-temperature and high-temperature processes in the formation of 3,4-benzopyrene during wood pyrolysis].

In 4 series of experiments a dependence between 3,4-benzpyrene (BP) output and the temperature of fir sawdust pyrolysis under isothermic conditions has been investigated. The experimental series differed in the duration of wood pulp particles stay in the reaction zone (tau). Also EPR spectra of pyrolysis products have been recorded. The experimental series did not differ in an output of ether extract from pyrolysis products, while BP output temperature curves in their shape were found to be largely dependent on tau: with an increased tau these curves definitely showed the maximum in the range of 300-350 degrees C and the BP output raised in the range of this maximum and also at the temperature of 600 degrees C. In the temperature range over 350 degrees C the character of dependence of the EPR signal value on temperature would correlate well with the temperature-dependent BP output, in the range of lower temperatures the EPR signal was not detected. The data obtained are considered as an evidence of two processes of BP formation in wood pyrolysis-a high-temperature process (temperature over 500 degrees C) and low-temperature one (300-350 degrees C). The high-temperature process seems to have the free-radical mechanism of BP formation, whereas in low temperatures it is evidently the result of a ion type reaction.

Benzopyrenes↗

Energy and nutrient recovery from sewage sludge via pyrolysis.

Energy recovery and nutrient reuse from sewage sludge has traditionally been achieved via anaerobic digestion/power generation with land application of the biosolids. By contrast, thermal processes such as pyrolysis have typically been used only for energy recovery. One such technology has demonstrated at commercial scale that all of the energy in sludge can be beneficially recovered and reused. No attempt was however made to recover and reuse sludge nutrients. There are many potential benefits of using pyrolysis for both energy and nutrient recovery. Firstly, unlike digestion, the principal energy product is oil, which can readily be stored and used when required, ensuring that energy recovery is maximised. Secondly is that the sludge nutrients are recovered in the pyrolysis char. Laboratory soil incubation studies using char from the Subiaco demonstration plant were conducted over an eight-week period to confirm nutrient availability. Results from this study showed that the phosphorus in the char is plant available although the nitrogen was insoluble. Based on these results it appears that there is potential to use pyrolysis as an effective means to recover and reuse both the energy and the very valuable phosphorus present in sewage sludges.

Agriculture↗

Pyrolysis gas chromatography -- a potential technique for characterization of complex organic material.

A pyrolysis gas chromatography (PGC) technique is described and various pyrolysers discussed. Results from analyses of synthetic polymers and organic salts are given. The influence of temperature rise time, pyrolysis temperature, pyrolysis time and sample size is considered. Pyrolysis studies on microorganisms are described various ways of improving the technique are considered.

Chromatography, Gas↗

Analysis of t-butylphenol acetylene condensed resin with methyl-methine linkages in vulcanized rubber by pyrolysis-gas chromatography/mass spectrometry

Methyl-methine linkages of Novolac, a commercially available t-butylphenol acetylene condensed (TBPA) resin, have been identified by recognition of pyrolysis pathways using pyrolysis-gas chromatography/mass spectrometry (Py-GC/mS) in vulcanized rubber. The diagnostic mass spectrum of t-butylphenol with methyl-methine linkages between phenolic rings was observed at m/z 192, corresponding to 4-t-butyl-2-ethyl-6-methylphenol. Other molecular ions were observed at m/z 178, 164, and 150 in the characteristic pyrolyzates. The ion at m/z 192 in the TBPA resin was observed to be characteristic for methyl-methine linkages between the phenolic groups, and the analytical pyrolysis-GC/mS method was thus able to identify the resin at low levels in vulcanized rubber. Copyright 1999 John Wiley & Sons, Ltd.

Journal Article↗

Study of thermal behavior of vitamin D3 by pyrolysis-GC-MS in combination with boiling point-retention time correlation.

The thermal behavior of vitamin D3 was studied based on pyrolysis-GC-MS technique. It was pyrolyzed at 600 degrees C, 750 degrees C, 900 degrees C, respectively. The pyrolysis product were separated With an HP-5 column and identified by the NIST mass spectral search program in combination with the correlation of boiling point and retention time (BP-RT). There are totally 50 components, including mono aromatics and polycyclic aromatic hydrocarbons (PAHs), were determined. It is shown that the contents of the PAHs are increasing with the increasing of the pyrolysis temperature. The contents of the determined components vary from 0.04% to 37.08%.

Cholecalciferol↗

Gas-phase detection of HSOH: synthesis by flash vacuum pyrolysis of di-tert-butyl sulfoxide and rotational-torsional spectrum.

Gas-phase oxadisulfane (HSOH), the missing link between the well-known molecules hydrogen peroxide (HOOH) and disulfane (HSSH), was synthesized by flash vacuum pyrolysis of di-tert-butyl sulfoxide. Using mass spectrometry, the pyrolysis conditions have been optimized towards formation of HSOH. Microwave spectroscopic investigation of the pyrolysis products allowed-assisted by high-level quantum-chemical calculations--the first measurement of the rotational-torsional spectrum of HSOH. In total, we have measured approximately 600 lines of the rotational-torsional spectrum in the frequency range from 64 GHz to 1.9 THz and assigned some 470 of these to the rotational-torsional spectrum of HSOH in its ground torsional state. Some 120 out of the 600 lines arise from the isotopomer H(34)SOH. The HSOH molecule displays strong c-type and somewhat weaker b-type transitions, indicating a nonplanar skew chain structure, similar to the analogous molecules HOOH and HSSH. The rotational constants (MHz) of the main isotopomer (A=202 069, B=15 282, C=14 840), determined by applying a least-squares analysis to the presently available data set, are in excellent agreement with those predicted by quantum-chemical calculations (A=202 136, B=15 279, C=14 840). Our theoretical treatment also derived the following barrier heights against internal rotation in HSOH (when in the cis and trans configurations) to be V(cis) approximately equal to 2216 cm(-1) and V(trans) approximately equal to 1579 cm(-1). The internal rotational motion results in detectable torsional splittings that are dependent on the angular momentum quantum numbers J and K(a).

Journal Article↗

Low-pressure pyrolysis of tBu2SO: synthesis and IR spectroscopic detection of HSOH.

Sulfenic acid (HSOH, 1) has been synthesized in the gas-phase by low-pressure high-temperature (1150 degrees C) pyrolysis of di-tert-butyl sulfoxide (tBu(2)SO, 2) and characterized by means of matrix isolation and gas-phase IR spectroscopy. High-level coupled-cluster (CC) calculations (CCSD(T)/cc-pVTZ and CCSD(T)/cc-pVQZ) support the first identification of the gas-phase IR spectrum of 1 and enable its spectral characterization. Five of the six vibrational fundamentals of matrix-isolated 1 have been assigned, and its rotational-resolved gas-phase IR spectrum provides additional information on the O-H and S-H stretching fundamentals. Investigations of the pyrolysis reaction by mass spectrometry, matrix isolation, and gas-phase FT-IR spectroscopy reveal that, up to 500 degrees C, 2 decomposes selectively into tert-butylsulfenic acid, (tBuSOH, 3), and 2-methylpropene. The formation of the isomeric sulfoxide (tBu(H)SO, 3 a) has been excluded. Transient 3 has been characterized by a comprehensive matrix and gas-phase vibrational IR study guided by the predicted vibrational spectrum calculated at the density functional theory (DFT) level (B3LYP/6-311+G(2d,p)). At higher temperatures, the intramolecular decomposition of 3, monitored by matrix IR spectroscopy, yields short-lived 1 along with 2-methylpropene, but also H(2)O, and most probably sulfur atoms. In addition, HSSOH (6), H(2), and S(2)O are found among the final pyrolysis products observed at 1150 degrees C in the gas phase owing to competing intra- and intermolecular decomposition routes of 3. The decomposition routes of the starting compound 2 and of the primary intermediate 3 are discussed on the basis of experimental results and a computational study performed at the B3LYP/6-311G* and second-order Møller-Plesset (MP2/6-311G* and RI-MP2/QZVPP) levels of theory.

Journal Article↗

Identifying acetylated lignin units in non-wood fibers using pyrolysis-gas chromatography/mass spectrometry.

A series of non-wood plant fibers, namely kenaf, jute, sisal and abaca, have been analyzed upon pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) of the whole material. The pyrolysis products mainly arise from the carbohydrate and lignin moieties of the fibers. The lignin-derived phenols belonged to the p-hydroxyphenylpropanoid (H), guaiacylpropanoid (G) and syringylpropanoid (S) structures, and showed a high S/G ratio of between 2.0 and 5.4, the highest corresponding to kenaf. Among the lignin-derived phenols released, small amounts of sinapyl and coniferyl acetates (in both cis- and trans-forms) were identified for the first time upon Py-GC/MS of lignocellulosic materials. Acetylation of the sinapyl and coniferyl alcohols was at the gamma-position of the side chain. The release of these alcohols derived from intact acetylated lignin units upon pyrolysis seems to indicate that the native lignin in the fibers selected for this study is at least partially acetylated. Sinapyl (and coniferyl) acetates have recently been suggested to be authentic lignin precursors involved in the polymerization of lignin along with the normal sinapyl and coniferyl alcohols. Py-GC/MS will offer a convenient and rapid tool for analyzing naturally acetylated lignins, as well as to screen plant materials for the presence of acetylated units in lignin.

Acetylation↗

Pyrolysis-gas chromatography/mass spectrometry of fractions separated from a low-temperature coal tar: an attempt to develop a general method for characterising structures and compositions of heavy hydrocarbon liquids.

A low-temperature coal tar has been fractionated by column chromatography into acetonitrile, pyridine and 1-methyl-2-pyrrolidinone- (NMP) solubles. The tar and its fractions have been examined by pyrolysis-gas chromatography/mass spectrometry (GC/MS). Fractionation by planar chromatography was also carried out for purposes of comparison. Molecular masses of the fractions were estimated by size-exclusion chromatography (SEC), and bulk structural characterisation was carried out by (13)C-NMR and UV-fluorescence spectrometry. SEC showed that the fractions shifted to progressively shorter elution times (higher apparent masses) with diminishing solubility, i.e. from acetonitrile to NMP solubles. UV-fluorescence spectra showed parallel shifts to longer wavelengths and lower fluorescence quantum yields, indicating increasing sizes of aromatic ring systems and increasingly complex molecules. GC/MS analysis of the tar showed alkanes from C10 to C32 and extensive series of alkylated aromatics, phenols, indenes, naphthalenes, phenanthrenes and fluoranthenes. Pyrolysis-GC/MS results for the acetonitrile solubles closely resembled the data for the tar sample, with extensive series of alkylated benzenes, phenols and naphthalenes as well as alkanes from C16 to C28. The pyridine-soluble fraction showed no significant aromatic pyrolysis products and only relatively weak signals for alkanes between C16 and C27. The NMP-soluble fraction showed even less overall signal, with no significant aromatic components and weak signals for alkanes between C21 and C25, even though (13)C-NMR analyses showed that approximately half of the carbon detected was aromatic. The aliphatics are assumed to provide bridging structures between polycyclic aromatic (PCA) ring systems.

Journal Article↗

Changes in Hydration Properties of Silica Gel in a Process of Its Carbonization by Pyrolysis of Acetylacetone Zn (Ti) Acetylacetonates.

Changes in hydration properties of different compounds in a process of formation of a complex adsorbent comprising carbon and TiO2 or Zn2SiO4 on its surface were studied by 1H NMR spectroscopy under conditions of a liquid phase freezing. Adsorbents were synthesized on the basis of a mesoporous silica gel, the surface of which was covered with a carbon layer formed in a process of a high temperature pyrolysis of acetylacetone. Titanium oxide and zinc silicate on the surface of a parent silica gel were formed by a pyrolysis of acetylacetonates of the corresponding metals. It has been revealed that the main types of surface-active sites for the adsorbed water molecules on the carbosil surface are the systems of condensed benzene nuclei of a carbon component of the surface and hydroxyl groups of silica surface. Zn2SiO4 and TiO2 have been formed in a process of pyrolysis of the corresponding metal acetylacetonates. Water bound with the oxide component of the carbosil surface exceeds 80% of the total amount of the adsorbed water. The carbon component of the surface is localized mainly in the narrowest pores. A minimum value in the free surface energy was recorded for the carbosil sample. Copyright 1998 Academic Press.

Journal Article↗

Identification of natural dyes used in works of art by pyrolysis-gas chromatography/mass spectrometry combined with in situ trimethylsilylation.

Samples of four natural dyes from different organic families--natural madder (anthraquinonoid), curcuma (curcuminoid), saffron (carotenoid) and indigo (indigotic)--were analysed using a new procedure based on pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS), which includes the on-line derivatisation of the natural dyes using hexamethyldisilazane (HMDS). In addition, a previous procedure involving the addition of a 10% H2SO4 aqueous solution to the dye and further separation with ethyl acetate has been tested. This procedure enhances the sensitivity of the method by extracting the colouring compounds from the rest of the compounds present in the natural dye. Two possible derivatising reagents--HMDS and tetramethylammonium hydroxide (TMAH)--were compared in order to assess their effectiveness in the proposed method. Characteristic peaks from trimethylsilyl derivatives of alizarin, quinizarin, xanthopurpurin and purpurin were obtained for madder; peaks from safranal, isophorone and trimethylsilyl derivative of crocetin for saffron; peaks from 4-(4-hydroxy-3-methoxy)phenyl-3-buten-2-one and 4-(4-hydroxy-3-methoxy)phenyl-2-butanone, which are primary pyrolysis products of curcuma, and peaks from indole, 2-methylindole and 2,3-dihydroindol-2-one, which are primary pyrolysis products of indigo, among others, were obtained. The reported procedure leads to the unambiguous identification of the four studied dyes from solid samples formed by individual dyes.

Journal Article↗

Identification and discrimination of oral asaccharolytic Eubacterium spp. by pyrolysis mass spectrometry and artificial neural networks.

Curie-point pyrolysis mass spectra were obtained from 29 oral asaccharolytic Eubacterium strains and 6 abscess isolates previously identified as Peptostreptococcus heliotrinreducens. Pyrolysis mass spectrometry (PyMS) with cluster analysis was able to clarify the taxonomic position of this group of organisms. Artificial neural networks (ANNS) were then trained by supervised learning (with the back-propagation algorithm) to recognize the strains from their pyrolysis mass spectra; all Eubacterium strains were correctly identified, and the abscess isolates were identified as un-named Eubacterium taxon C2 and were distinct from the type strain of P. heliotrinreducens. These results demonstrate that the combination of PyMS and ANNs provides a rapid and accurate identification technique.

Bacterial Typing Techniques↗

Rapid phenotypic characterization of Vibrio isolates by pyrolysis metastable atom bombardment mass spectrometry.

Pyrolysis mass spectrometry was investigated for rapid characterization of food-borne bacterial pathogens. Nine isolates of Vibrio parahaemolyticus and one isolate each of Vibrio fluvialis, Vibrio hollisae, and Vibrio vulnificus were analyzed. Pyrolysis mass spectra, generated via an alternative ionization method, metastable atom bombardment, were subject to principal component-discriminant analysis. The spectral patterns were used to distinguish Vibrio isolates differing in species, serotype and expression of the thermostable direct hemolysin gene. The patterns of similarity and dissimilarity amongst spectra in the Vibrio test set generally reflected those associated with species, serotype or hemolysin-producing genes, though the combined influence of these and other variables in the multi-dimensional data did not produce a simple clustering with respect to any one of these characteristics. These results suggested that with enough examples to model the most common combinations, the method should be able to characterize Vibrio isolates according to their phenotypic characteristics. Pyrolysis-mass spectrometry with metastable atom bombardment and pattern recognition appeared suitable for rapid infraspecific comparison of Vibrio isolates. This integrated analytical, pattern-recognition system should be examined further for potential utility in clinical and public health diagnostic contexts.

Animals↗

Steranes and triterpanes generated from kerogen pyrolysis in the absence and presence of minerals.

Steranes and triterpanes generated from pyrolysis of immature Monterey Formation kerogen in the presence and absence of calcite, illite and montmorillonite reveal results that are both consistent and divergent with published data that reflect the use of these biological markers as maturation indicators. The extent of isomerization of biomarkers generated from pyrolysis of kerogen at 300 degrees C for 2 hours, at C-20 in 14 alpha(H), 17 alpha(H)-steranes, at C-22 in 17 alpha(H),21 beta(H)-hopanes and of 17 beta(H),21 beta(H)-hopanes correspond to early diagenetic stages in rock extracts from sedimentary basins. Isomerization increases with heating time and, after 1000 hours, attains values which correspond to the catagenetic stage in sedimentary basins, or equivalent to that of mature oil. Stepwise pyrolysis of the kerogen indicates faster isomerization rates for steranes and triterpanes in the bitumen than those retained in the kerogen structure, confirming earlier studies. Presence of a mineral matrix can influence the isomerization of steranes and triterpanes considerably. Comparisons with results from kerogen heated alone, for a given maturation stage, show that calcite inhibits, illite catalyzes slightly and montmorillonite has a pronounced catalytic effect on these reactions. This effect results in early isomerization of steranes and hopanes corresponding to the catagenetic stage in the presence of montmorillonite, while kerogen or kerogen with calcite held at the same temperature (300 degrees C) and time (10 hours) only yield isomerized products which correspond to a diagenetic stage. Further, illite and montmorillonite affect various isomerization reactions differently. The fastest reaction is the isomerization at C-20 in 14 alpha(H),17 alpha (H)-steranes followed by that at C-22 in 17 alpha(H),21 beta(H)-hopanes and the slowest is the formation of 14 beta(H),17 beta(H) steranes. These results show that maturation measurements of rock or oil samples from basins which use biological markers have to take into account the mineral matrix effects, which have been largely ignored until present.

Bentonite↗

Pyrolysis mass spectra, sulfhydryl and tryptophan content of the embryonic nuclei from adult human normal and nuclear-cataractous lenses.

Cataractous state-related alterations were studied by Curie-point pyrolysis low voltage mass spectrometry performed on the embryonic nuclei from adult normal and nuclear-cataractous human lenses. It was shown that the relative intensities of ion signals assigned to sulfur dioxide and tentatively, to other sulfur oxidation products correlate with the increase in lens nuclear color. Since these ion signals may represent pyrolysis fragments from methionine sulfoxide, methionine sulfone, cysteic acid and disulfide compounds present in the parent material, it is concluded that progressive oxidation of sulfur compounds appears to take place during nuclear cataractogenesis. Automated pyrolysis mass spectrometry coupled with multivariate analysis of the spectral data by computer turned out to be a rapid method of characterizing sub-milligram samples of lens material. The results were supported by data obtained by conventional determination of sulfhydryl and tryptophan groups.

Cataract↗

Volatilisation of alkali and alkaline earth metallic species during the pyrolysis of biomass: differences between sugar cane bagasse and cane trash.

Sugar cane bagasse and cane trash were pyrolysed in a novel quartz fluidised-bed/fixed-bed reactor. Quantification of the Na, K, Mg and Ca in chars revealed that pyrolysis temperature, heating rate, valence and biomass type were important factors influencing the volatilisation of these alkali and alkaline earth metallic (AAEM) species. Pyrolysis at a slow heating rate (approximately 10 K min(-1)) led to minimal (often <20%) volatilisation of AAEM species from these biomass samples. Fast heating rates (>1000 K s(-1)), encouraging volatile-char interactions with the current reactor configuration, resulted in the volatilisation of around 80% of Na, K, Mg and Ca from bagasse during pyrolysis at 900 degrees C. Similar behaviour was observed for monovalent Na and K with cane trash, but the volatilisation of Mg and Ca from cane trash was always restricted. The difference in Cl content between bagasse and cane trash was not sufficient to fully explain the difference in the volatilisation of Mg and Ca.

Bioelectric Energy Sources↗