Formation and Prediction of PhIP, Harman, and Norharman in Chemical Model Systems Containing Epicatechin under Various Reaction Conditions

Author(s):  
Teng Hui ◽  
Yanlei Li ◽  
Ruixia Chen ◽  
Xiaoyue Yang ◽  
Huan Liu ◽  
...  
2009 ◽  
Vol 27 (Special Issue 1) ◽  
pp. S207-S210
Author(s):  
K. Cejpek ◽  
J. Velíšek

This study is focused on the reactions of isothiocyanates (ITCs) in the presence of amino compounds leading to coloured structures <I>via</I> substituted 2-thiohydantoins. A series of complementary experiments has been done and appropriate reaction conditions and structural prerequisites have been defined. Low-molecular colourants isolated and characterised from the model systems can be sorted into three groups. Yellow to red diastereomeric dehydrodimers of 2-thiohydantoin derivatives that contain an acidic methylene group are formed in mixtures consisted of ITCs and amino acids with &alpha;-methylene group in mild acidic to mild alkaline systems. The condensation products of the 2-thiohydantoins with reactive aromatic or heterocyclic carbaldehydes from the Maillard reaction, essential oils etc. comprise a heterogeneous group of mostly yellow colourants. Blue compounds of two types are structurally more complicated structures that arise from <I>N</I>-substituted amino acids and ITCs in alkaline media.


2021 ◽  
Vol 427 ◽  
pp. 133013
Author(s):  
Johannes Reiff ◽  
Robin Bardakcioglu ◽  
Matthias Feldmaier ◽  
Jörg Main ◽  
Rigoberto Hernandez

2009 ◽  
Vol 47 (4) ◽  
pp. 458-467 ◽  
Author(s):  
Andreas Daiber ◽  
Stefan Schildknecht ◽  
Johanna Müller ◽  
Jens Kamuf ◽  
Markus M. Bachschmid ◽  
...  
Keyword(s):  

2004 ◽  
Vol 52 (22) ◽  
pp. 6837-6842 ◽  
Author(s):  
Fabien Robert ◽  
Gilles Vuataz ◽  
Philippe Pollien ◽  
Françoise Saucy ◽  
Maria-Isabelle Alonso ◽  
...  

2007 ◽  
Vol 3 (2) ◽  
pp. 70-73 ◽  
Author(s):  
Eric T Kool ◽  
Marcey L Waters
Keyword(s):  

2021 ◽  
Vol 13 (6) ◽  
pp. 3583
Author(s):  
Pegah Zahedifar ◽  
Lukasz Pazdur ◽  
Christophe M.L. Vande Velde ◽  
Pieter Billen

The use of polyurethanes and, therefore, the quantity of its scrap are increasing. Considering the thermoset characteristic of most polyurethanes, the most circular recycling method is by means of chemical depolymerization, for which glycolysis is finding its way into the industry. The main goal of polyurethane glycolysis is to recover the polyols used, but only limited attempts were made toward recovering the aromatic dicarbamate residues and derivates from the used isocyanates. By the split-phase glycolysis method, the recovered polyols form a top-layer phase and the bottom layer contain transreacted carbamates, excess glycol, amines, urea, and other side products. The hydrolysis of carbamates results in amines and CO2 as the main products. Consequently, the carbamates in the bottom layer of polyurethane split-phase glycolysis can also be hydrolyzed in a separate process, generating amines, which can serve as feedstock for isocyanate production to complete the polyurethane material cycle. In this paper, the full recycling of polyurethanes is reviewed and experimentally studied. As a matter of demonstration, combined glycolysis and hydrolysis led to an amine production yield of about 30% for model systems. With this result, we show the high potential for further research by future optimization of reaction conditions and catalysis.


1982 ◽  
Vol 13 (49) ◽  
Author(s):  
T. G. TRAYLOR ◽  
M. J. MITCHELL ◽  
J. P. CICCONE ◽  
S. NELSON
Keyword(s):  

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