1967
DOI: 10.1246/nikkashi1898.70.12_2348
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Ozonization of Lignin Model Compounds

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Cited by 9 publications
(8 citation statements)
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“…Ozone oxidation has been used extensively in the paper and pulping industry as a bleaching agent and in the pretreatment of the paper wastewater. Ozone reportedly attacks lignin model compounds at the C3–C4 position of aromatic ring forming muconic acid derivatives. Different types of lignin model compounds have different reactivity toward ozone, and α-carbonyl type compounds are more stable than benzyl alcohol type compounds. , On this basis, we postulated that the treatment of lignin particles with ozone in an aqueous solution would result in activated aromatic rings at the surface of lignin particles that would be selectively cleaved to produce carboxyl groups, while aromatic rings within lignin particles would be less subject to attack from ozone within the limited treatment time. The resulting newly formed carboxyl groups would then improve the solubility of the lignin and offer a site for esterification.…”
Section: Introductionmentioning
confidence: 99%
“…Ozone oxidation has been used extensively in the paper and pulping industry as a bleaching agent and in the pretreatment of the paper wastewater. Ozone reportedly attacks lignin model compounds at the C3–C4 position of aromatic ring forming muconic acid derivatives. Different types of lignin model compounds have different reactivity toward ozone, and α-carbonyl type compounds are more stable than benzyl alcohol type compounds. , On this basis, we postulated that the treatment of lignin particles with ozone in an aqueous solution would result in activated aromatic rings at the surface of lignin particles that would be selectively cleaved to produce carboxyl groups, while aromatic rings within lignin particles would be less subject to attack from ozone within the limited treatment time. The resulting newly formed carboxyl groups would then improve the solubility of the lignin and offer a site for esterification.…”
Section: Introductionmentioning
confidence: 99%
“…These quinoids again decompose to aliphatic products with carbonyl and carboxyl groups due to opening of an aromatic ring. 109 Ozone can also attack molecular sites with an electron deficit (such as -COO -) and, more frequently, at sites with carbon carrying electronwithdrawing groups (such as -NH 3 + , -NO 2 , -CN, -SO 3 H, etc).…”
Section: A Final Ozonide (Iv) Can Be Produced By Another 13-cycloaddmentioning
confidence: 99%
“…attack on phenol via electrophilic substitution 109. To increase the concentration of hydroxyl radicals, ozone is activated with UV, H 2 O 2 , and various catalysts such as activated carbon, alumina, Ferral, platinised TiO 2 .…”
mentioning
confidence: 99%
“…The degree of destruction depends on the medium in which the ozonization is carried out and on the type of lignin used. Moreover, ozone can also react with double bonds in the side-chain of phenyl-propane units, which are more reactive than the aromatic rings (Hatakeyama, 1967). Lignin is reported to have one double bond per 40-60 C, monomeric units (Tiscenko, 1959).…”
Section: Figure 4 Ir Spectra Of the Original And Ozonized Ligninmentioning
confidence: 99%