2007
DOI: 10.1016/j.jaap.2007.03.001
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Evaluate the pyrolysis pathway of glycine and glycylglycine by TG–FTIR

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Cited by 148 publications
(80 citation statements)
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“…The first peaks were attributed to deamination of pristine molecules, and the second to secondary pyrolysis reactions. However, different from [20] we did not find a pronounced deamination peak suggesting that the majority of free amine groups were already transformed into the amide and/or imide moiety before activation energy for direct deamination was reached. This was also supported by the unchanged C/N ratio of the 200 • C residue (Table 1).…”
Section: Offline-pyrolysis and Tga-ftircontrasting
confidence: 84%
See 1 more Smart Citation
“…The first peaks were attributed to deamination of pristine molecules, and the second to secondary pyrolysis reactions. However, different from [20] we did not find a pronounced deamination peak suggesting that the majority of free amine groups were already transformed into the amide and/or imide moiety before activation energy for direct deamination was reached. This was also supported by the unchanged C/N ratio of the 200 • C residue (Table 1).…”
Section: Offline-pyrolysis and Tga-ftircontrasting
confidence: 84%
“…Furthermore, the evolution of NH 3 started during this decomposition step and exhibited a weak shoulder around 280 • C at the peak of maximum NH 3 release (360 • C). Pyrolysis of Gly and Gly-Gly also had two NH 3 release peaks at similar temperatures (260-285 • C, 360-380 • C) [20]. The first peaks were attributed to deamination of pristine molecules, and the second to secondary pyrolysis reactions.…”
Section: Offline-pyrolysis and Tga-ftirmentioning
confidence: 90%
“…34 Although one-to-one correspondence of the observed differential thermogravimetric (DTG) peaks in the present study to these sequence is not possible at present, the DTG peak shift to the lower temperature side and increased separation of the peaks observed might imply the decomposition promotion due to the thermocatalytic action of the titania substrate and the complex formation. This is attributed to the specific binding of the molecular fractions, due to the specific adsorption configuration.…”
Section: Discussionmentioning
confidence: 54%
“…It has been postulated that the combined study of biomass and amino acids is the best approach to grasp a more comprehensive mechanism of nitrogen chemistry in biomass components (N-Chemistry) (Becidan et al, 2007). While the pyrolysis of amino acids has been extensively studied, there is very little information on the product distribution from the co-pyrolysis of amino acids with other forms of biomass (Li et al, 2007;Ren et al, 2011). Thus, this study attempts to bridge this gap in a more detailed manner.…”
Section: Introductionmentioning
confidence: 99%
“…Thus, this study attempts to bridge this gap in a more detailed manner. Since most of the elemental nitrogen is bound in proteins, co-pyrolysis of lignin + tyrosine, ethyl cellulose + tyrosine, and sodium alginate + tyrosine was conducted with the aim of finding features that are protein-specific (Li et al, 2007;Hansson et al, 2003Hansson et al, , 2004. Notably, the studies of the pyrolysis of some biomass constituents such as tyrosine, laminarin and sodium alginate are scarce in literature.…”
Section: Introductionmentioning
confidence: 99%