1998
DOI: 10.1016/s0021-9673(98)00268-4
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Structural characterization of bio- and geo-macromolecules by off-line thermochemolysis with tetramethylammonium hydroxide

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Cited by 130 publications
(91 citation statements)
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“…Py/TMAH induces cleavage of alkyl aryl ether bonds in lignin and releases products similar to those obtained upon CuO alkaline degradation, including methylated hydroxybenzaldehydes (peaks 6, 12 and 18), hydroxyacetophenones (peaks 15 and 22) and hydroxybenzoic acids (peaks 10, 16 and 24). 13,14,49,50 As seen in Figure 2, Py/TMAH of the cortex and pith released high amounts (over 45% of the total peak area) of the fully methylated derivative of p-coumaric acid, i.e., trans-3-(4-methoxyphenyl)propenoic acid methyl ester, or methyl trans-4-O-methyl-p-coumarate (peak 23), as well as lower amounts (nearly 5% of total peak area) of the fully methylated derivative of ferulic acid, i.e., trans-3-(3,4-dimethoxyphenyl)propenoic acid methyl ester, or methyl 4-O-methyl-ferulate (peak 29). In addition to the trans-forms of methylated p-hydroxycinnamic acids, minor amounts of the cis-isomers (peaks 17 and 26) were also identified.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…Py/TMAH induces cleavage of alkyl aryl ether bonds in lignin and releases products similar to those obtained upon CuO alkaline degradation, including methylated hydroxybenzaldehydes (peaks 6, 12 and 18), hydroxyacetophenones (peaks 15 and 22) and hydroxybenzoic acids (peaks 10, 16 and 24). 13,14,49,50 As seen in Figure 2, Py/TMAH of the cortex and pith released high amounts (over 45% of the total peak area) of the fully methylated derivative of p-coumaric acid, i.e., trans-3-(4-methoxyphenyl)propenoic acid methyl ester, or methyl trans-4-O-methyl-p-coumarate (peak 23), as well as lower amounts (nearly 5% of total peak area) of the fully methylated derivative of ferulic acid, i.e., trans-3-(3,4-dimethoxyphenyl)propenoic acid methyl ester, or methyl 4-O-methyl-ferulate (peak 29). In addition to the trans-forms of methylated p-hydroxycinnamic acids, minor amounts of the cis-isomers (peaks 17 and 26) were also identified.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The aromatic compounds identified in HULIS were remarkably similar to pyrolysis products of HAs, FAs and lignin (Martin et al, 1994(Martin et al, , 1995del Rio et al, 1998;Chefetz et al, 2002;Li et al, 2006;Fukushima et al, 2011). All HULIS pyrograms present two distinct peaks at 32.8 min and 34.5 min (Nos.…”
Section: Sample Functional Groups (%)mentioning
confidence: 87%
“…have also been detected in water soluble organic compounds in organic aerosol (Gelencser et al, 2000;Subbalakshmi et al, 2000) and in dissolved organic matter in river water or rainwater (del Rio et al, 1998). The aromatic compounds identified in HULIS were remarkably similar to pyrolysis products of HAs, FAs and lignin (Martin et al, 1994(Martin et al, , 1995del Rio et al, 1998;Chefetz et al, 2002;Li et al, 2006;Fukushima et al, 2011).…”
Section: Sample Functional Groups (%)mentioning
confidence: 92%
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“…Since its first introduction, pyrolysis-methylation has been applied to many different biopolymers [9 -11], humic materials [12,13], whole soils [14 -15], asphaltenes, kerogens, and coals [13,16] and resins and resinites [9,17].…”
Section: Introductionmentioning
confidence: 99%