Catalytic Oxidation of Lignin and Model Compounds over Nano Europium Oxide

Author(s):  
Qingmeng Dong ◽  
Zhouqi Tian ◽  
Wulin Song ◽  
Weiping Deng ◽  
Hongxi Zhang
2003 ◽  
Vol 47 (1) ◽  
pp. 179-184 ◽  
Author(s):  
J.S. Park ◽  
H. Choi ◽  
K.H. Ahn

The sorption and catalytic oxidation of model compounds (pCBA and phenanthrene) and NOM on FeOOH were investigated using hydrogen peroxide and ozone, respectively. After oxidation with ozone, the hydrophobic, transphilic, and hydrophilic NOM fractions were isolated using XAD-8 and -4 resins to analyze the reaction characteristics. The sorption of pCBA was strongly dependent upon the pH, but phenanthrene exhibited a sorption behavior that was independent of the pH. In the case of NOM, the hydrophobic portion showed higher sorption affinity than hydrophilic and transphilic at pH 7.2. The concentrations of model compounds and oxidants were measured during the oxidations and the efficiency was compared for tests done with ozone alone and those using catalytic ozonation. Through the comparison of the sorption and decomposition of the model compounds, along with the effects of bicarbonate addition, mechanisms for catalytic oxidation with hydrogen peroxide or ozone were proposed, respectively.


2010 ◽  
Vol 84 (9) ◽  
pp. 1511-1515
Author(s):  
K. G. Bogolitsyn ◽  
M. A. Aizenshtadt ◽  
A. N. Pryakhin ◽  
V. V. Lunin ◽  
S. A. Pokryshkin

2015 ◽  
Vol 13 (11) ◽  
pp. 3243-3254 ◽  
Author(s):  
Nikhil D. Patil ◽  
Soledad G. Yao ◽  
Mark S. Meier ◽  
Justin K. Mobley ◽  
Mark Crocker

Selective, catalytic oxidation of benzylic –OH groups followed by Baeyer–Villiger oxidation cleaves the β-O-4 linkage in lignin model compounds.


2019 ◽  
Vol 9 (2) ◽  
pp. 384-397 ◽  
Author(s):  
Edwin B. Clatworthy ◽  
Julia L. Picone-Murray ◽  
Alexander K. L. Yuen ◽  
Richard T. Maschmeyer ◽  
Anthony F. Masters ◽  
...  

The catalytic oxidation of lignin model compounds by Co/Br−/H2O2 is investigated; substituting Br− for N-hydroxyphthalimide improved substrate conversion and product yield.


2020 ◽  
Author(s):  
Raku Irie ◽  
Kei Miyako ◽  
Satoko Matsunaga ◽  
Ryuichi Sakai ◽  
Masato Oikawa

<div>Here, we newly propose the structure of protoaculeine B, an N-terminal moiety of the marine peptide toxin aculeine B, as possessing the cis-disubstituted tetrahydro-beta-carboline framework. We prepared two truncated model compounds that lack long-chain polyamine by one-step Pictet-Spengler reaction of tryptophan, and compared the NMR and mass spectra and chemical reactivity with those of natural protoaculeine B. The synthetic models reproduced the profiles of the natural product well, which was conclusive for the structural revision.</div>


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