SOURCES OF HYDROGEN DONORS AND THEIR EFFECTS ON DENITRIFICATION RATES

Author(s):  
James L. Barnard ◽  
P.G.J. Meiring
Keyword(s):  
2020 ◽  
Vol 7 (1) ◽  
pp. 29-36
Author(s):  
Antonina A. Stepacheva ◽  
Mariia E. Markova ◽  
Yury V. Lugovoy ◽  
Kirill V. Chalov ◽  
Mikhail G. Sulman ◽  
...  

AbstractHydrotreatment of bio-oil oxygen compounds allows the final product to be effectively used as a liquid transportation fuel from biomass. Deoxygenation is considered to be one of the most promising ways for bio-oil upgrading. In the current work, we describe a novel approach for the deoxygenation of bio-oil model compounds (anisole, guaiacol) using supercritical fluids as both the solvent and hydrogen-donors. We estimated the possibility of the use of complex solvent consisting of non-polar n-hexane with low critical points (Tc = 234.5 ºC, Pc = 3.02 MPa) and propanol-2 used as H-donor. The experiments were performed without catalysts and in the presence of noble and transition metals hydrothermally deposited on the polymeric matrix of hypercrosslinked polystyrene (HPS). The experiments showed that the presence of 20 vol. % of propanol-2 in n-hexane results in the highest (up to 99%) conversion of model compounds. When the process was carried out without a catalyst, phenols were found to be a major product yielding up to 95 %. The use of Pd- and Co-containing catalyst yielded 90 % of aromatic compounds (benzene and toluene) while in the presence of Ru and Ni cyclohexane and methylcyclohexane (up to 98 %) were the main products.


2015 ◽  
Vol 68 (11) ◽  
pp. 1640 ◽  
Author(s):  
Eietsu Hasegawa ◽  
Shin-ya Takizawa

2-Aryl-1,3-dimethylbenzimidazolines (DMBIHs) have been applied to photoinduced electron-transfer reductions of various organic substrates. Either direct or indirect electron transfer between the substrates and DMBIHs is utilized to promote the desired transformations. Photoexcitation of the substrates using light above 280 nm was carried out in the former protocol whereas a photosensitization method using materials such as substituted pyrenes, ruthenium and iridium complexes that absorb longer-wavelength light was employed in the latter. In these reactions, DMBIHs undergo initial electron transfer and subsequent proton or hydrogen atom transfer.


Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 671 ◽  
Author(s):  
Eszter Baráth

Hydrogen transfer reactions have exceptional importance, due to their applicability in numerous synthetic pathways, with academic as well as industrial relevance. The most important transformations are, e.g., reduction, ring-closing, stereoselective reactions, and the synthesis of heterocycles. The present review provides insights into the hydrogen transfer reactions in the condensed phase in the presence of noble metals (Rh, Ru, Pd) as catalysts. Since the H-donor molecules (such as alcohols/ethers and amines (1°, 2°, 3°)) and the acceptor molecules (alkenes (C=C), alkynes (C≡C), and carbonyl (C=O) compounds) play a crucial role from mechanistic viewpoints, the present summary points out the key mechanistic differences with the interpretation of current contributions and the corresponding historical achievements as well.


Nature ◽  
1954 ◽  
Vol 173 (4407) ◽  
pp. 720-723 ◽  
Author(s):  
D. KEILIN ◽  
E. F. HARTREE
Keyword(s):  

2019 ◽  
Vol 85 (2) ◽  
pp. 508-514 ◽  
Author(s):  
Xiuwen Chen ◽  
Zhihai Yang ◽  
Xuyan Chen ◽  
Wanyi Liang ◽  
Zhongzhi Zhu ◽  
...  

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