Characterization of tetramethylammonium hydroxide thermochemolysis products of near-shore marine sediments using gas chromatography mass spectrometry and gas chromatography combustion/isotope ratio mass spectrometry

被引:36
作者
Pulchan, J
Abrajano, TA
Helleur, R
机构
[1] MEM UNIV NEWFOUNDLAND,DEPT CHEM,ST JOHNS,NF A1B 3X7,CANADA
[2] MEM UNIV NEWFOUNDLAND,DEPT EARTH SCI,ST JOHNS,NF A1B 3Z5,CANADA
关键词
tetramethylammonium hydroxide; thermochemolysis; lipid; lignin; marine sediments; gas chromatography mass spectrometry; gas chromatography combustion isotope ratio mass spectrometry; carbon isotope;
D O I
10.1016/S0165-2370(97)00051-X
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The study describes the application of gas chromatography/mass spectrometry (GC/MS) and gas chromatography/combustion/isotope ratio mass spectrometry (GC/C/IRMS) to characterize the molecular and compound-specific stable carbon isotope composition, respectively, of tetramethylammonium hydroxide (TMAH) thermochemolysis products of organic matter present in marine sediments. The objective of the study was to examine the usefulness of TMAH thermochemolysis products in identifying organic markers of terrestrial-derived sources in marine sediments. 'Batch-wise' thermochemolysis conditions (excess TMAH, 250 degrees C, sealed glass tube, 30 min) were used on sediments and standards. Compound-specific isotope analysis (CSIA) of standards showed no evidence of isotopic fractionation at methyl carbon during methylation of a number of phenolic acid and fatty acid compounds. It was also shown that no appreciable isotopic affect occurs during bond cleavage and methylation of fatty acid groups of the standard triglyceride, tricaprin. These preliminary tests indicate that the initial delta(13)C composition of chemical markers containing acidic functional groups can be obtained by measuring the delta(13)C Of the corresponding methyl esters and/or ethers after TMAH methylation. In order to confirm the number of methoxy groups in lignin-derived markers, tetraethylammonium hydroxide was employed. Useful chemical markers found in near-shore sediments in reasonable abundance were a range of fatty acids, vanillin, vanillic acid and p-coumaric acid. Preliminary results of CSIA of these phenolic markers and selected saturated fatty acids in three different marine sediment cores are reported. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:135 / 150
页数:16
相关论文
共 21 条
[1]   C-13 C-12 RATIOS IN INDIVIDUAL FATTY-ACIDS OF MARINE MYTILIDS WITH AND WITHOUT BACTERIAL SYMBIONTS [J].
ABRAJANO, TA ;
MURPHY, DE ;
FANG, J ;
COMET, P ;
BROOKS, JM .
ORGANIC GEOCHEMISTRY, 1994, 21 (6-7) :611-617
[2]   THE SCOPE OF PYROLYSIS METHYLATION REACTIONS [J].
CHALLINOR, JM .
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 1991, 20 :15-24
[3]   A NEW RAPID TECHNIQUE FOR THE CHARACTERIZATION OF LIGNIN IN VASCULAR PLANTS - THERMOCHEMOLYSIS WITH TETRAMETHYLAMMONIUM HYDROXIDE (TMAH) [J].
CLIFFORD, DJ ;
CARSON, DM ;
MCKINNEY, DE ;
BORTIATYNSKI, JM ;
HATCHER, PG .
ORGANIC GEOCHEMISTRY, 1995, 23 (02) :169-175
[4]   THE BEHAVIOR OF ESTERS IN THE PRESENCE OF TETRAMETHYLAMMONIUM SALTS AT ELEVATED-TEMPERATURES - FLASH PYROLYSIS OR FLASH CHEMOLYSIS [J].
DELEEUW, JW ;
BAAS, M .
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 1993, 26 (03) :175-184
[5]   GAS CHROMATOGRAPHIC - MASS SPECTROMETRIC STUDIES OF LONG CHAIN HYDROXY ACIDS .2. HYDROXY ACIDS AND FATTY ACIDS OF A 5000-YEAR-OLD LACUSTRINE SEDIMENT [J].
EGLINTON, G ;
HUNNEMAN, DH ;
DOURAGHI.K .
TETRAHEDRON, 1968, 24 (18) :5929-&
[6]   EVIDENCE FROM CARBON ISOTOPE MEASUREMENTS FOR DIVERSE ORIGINS OF SEDIMENTARY HYDROCARBONS [J].
FREEMAN, KH ;
HAYES, JM ;
TRENDEL, JM ;
ALBRECHT, P .
NATURE, 1990, 343 (6255) :254-256
[7]  
FRY B, 1984, CONTRIB MAR SCI, V27, P13
[8]  
Gearing J.N., 1988, Lecture Notes on Coastal and Estuarine Studies, V22, P69
[9]  
GONI MA, 1994, HRC-J HIGH RES CHROM, V17, P476
[10]   Comparison of two thermochemolytic methods for the analysis of lignin in decomposing gymnosperm wood: The CuO oxidation method and the method of thermochemolysis with tetramethylammonium hydroxide (TMAH) [J].
Hatcher, PG ;
Nanny, MA ;
Minard, RD ;
Dible, SD ;
Carson, DM .
ORGANIC GEOCHEMISTRY, 1995, 23 (10) :881-888