2013
DOI: 10.1134/s0018143913020070
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Aromatic products of radiation-thermal degradation of lignin and chitin

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Cited by 10 publications
(5 citation statements)
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“…For example, acetamide has been reported as a degradation product from both chitin , and N -acetylglucosamine and acetamide, N-(2,4-dihydroxyphenyl) from pyrolysis of chitin at 500 °C . Acetamide and acetic acid are possible products of pericyclic elimination. , Pyridinone derivatives can be a result of dehydration involving the acetamido group . The N -acetylglucosamine monomer released from chitin hydrolysis undergoes dehydration to form a furanic compound to which subsequently, oxygen–nitrogen exchange occurs, affording a 2-acetyl pyrrole ring, which was also detected in the biocrude from chitin HTL.…”
Section: Resultsmentioning
confidence: 99%
“…For example, acetamide has been reported as a degradation product from both chitin , and N -acetylglucosamine and acetamide, N-(2,4-dihydroxyphenyl) from pyrolysis of chitin at 500 °C . Acetamide and acetic acid are possible products of pericyclic elimination. , Pyridinone derivatives can be a result of dehydration involving the acetamido group . The N -acetylglucosamine monomer released from chitin hydrolysis undergoes dehydration to form a furanic compound to which subsequently, oxygen–nitrogen exchange occurs, affording a 2-acetyl pyrrole ring, which was also detected in the biocrude from chitin HTL.…”
Section: Resultsmentioning
confidence: 99%
“…As a result, NAG will be the major oligomer product within a short reaction time whereas glucosamine will be obtained with prolonged reaction time. Thermal chemical methods such as pyrolysis or radiolysis were also employed to convert chitin/chitosan [44][45][46]. Volatile aromatic heterocyclic compounds such as pyrazines, pyridines, pyrroles and furans were produced.…”
Section: Earlier Studiesmentioning
confidence: 99%
“…Pyrolysis or radiolysis of chitin/chitosan to produce volatile aromatic heterocyclic compounds such as pyrazines, pyridines, pyrroles and furans has been reported. [20][21][22] Nevertheless, these methods cannot achieve a selective degradation resulting in trace amounts of products. Hydrolysis of chitin by enzymes or concentrated acids affords NAG and oligomers, but this route suffers from low efficiency, environmental issues and limited product diversity.…”
Section: Introductionmentioning
confidence: 99%