1982
DOI: 10.1515/hfsg.1982.36.2.55
|View full text |Cite
|
Sign up to set email alerts
|

The Chemistry of Delignification - A General Concept - Part II

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
49
0
4

Year Published

2000
2000
2022
2022

Publication Types

Select...
5
5

Relationship

0
10

Authors

Journals

citations
Cited by 90 publications
(55 citation statements)
references
References 20 publications
2
49
0
4
Order By: Relevance
“…In acidic media, it forms a hydroxonium cation (Lachenal 1996;Gierer 1982), which is an electrophile and attacks the electron-rich sites of lignin, initiating such reactions as: ring hydroxylation, oxidative demethylation, oxidative ring opening, displacement of side chains, cleavage of β-aryl ether bonds, and epoxidation (Gierer 1982). The reduced viscosity of the pulps from hydrogen peroxide-aided treatments is presumably due to the formation of harmful radicals induced by high temperature and transition metals present in wood (Lachenal 1996).…”
Section: Hydrotropic Treatmentmentioning
confidence: 99%
“…In acidic media, it forms a hydroxonium cation (Lachenal 1996;Gierer 1982), which is an electrophile and attacks the electron-rich sites of lignin, initiating such reactions as: ring hydroxylation, oxidative demethylation, oxidative ring opening, displacement of side chains, cleavage of β-aryl ether bonds, and epoxidation (Gierer 1982). The reduced viscosity of the pulps from hydrogen peroxide-aided treatments is presumably due to the formation of harmful radicals induced by high temperature and transition metals present in wood (Lachenal 1996).…”
Section: Hydrotropic Treatmentmentioning
confidence: 99%
“…6). The subsequent steps include a reaction with the superoxide anion radical (O2· -) forming a hydroperoxide anion structure and its rearrangement to the primary oxidation products (oxirane, muconic acid ester, or carbonyl structures) (Chang and Gratzl 1980;Gierer 1982;Sixta et al 2006). The hydroperoxide structure, with a pKa value of 12 to 13, plays a crucial role, and has lately been shown to be the key intermediate in the course of phenolic lignin oxidation (Ji et al 2009a,b).…”
Section: Alkali-o2 Oxidationmentioning
confidence: 99%
“…During peroxyformic acid treatment, electrophilic HO + ions are formed (HCOOOH + H + = HCOOH + HO + ). According to model compound studies the main reactions for the HO + ions with lignin are expected to be ring hydroxylation, oxidative ring opening, substitution of side chains, cleavage of β-aryl ether bonds, and epoxidation (Gierer et al 1982;Hortling et al 1991;Strumila and Rapson 1975;Yuan et al 1998b).…”
Section: Papermaking Propertiesmentioning
confidence: 99%