Effect of phosphoric acid and acetic acid addition on the hydrogen evolution using Ni based catalyst prepared in ethanol, methanol, and water solvents

Author(s):  
Asım Balbay ◽  
Cafer Saka
2015 ◽  
Vol 396 ◽  
pp. 304-309 ◽  
Author(s):  
Ting Fang ◽  
Hai-Xia Lu ◽  
Jia-Xing Zhao ◽  
Shu-Zhong Zhan ◽  
Qi-Ying Lv

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Dong Tian ◽  
Yiyi Chen ◽  
Fei Shen ◽  
Maoyuan Luo ◽  
Mei Huang ◽  
...  

Abstract Background Peroxyacetic acid involved chemical pretreatment is effective in lignocellulose deconstruction and oxidation. However, these peroxyacetic acid are usually artificially added. Our previous work has shown that the newly developed PHP pretreatment (phosphoric acid plus hydrogen peroxide) is promising in lignocellulose biomass fractionation through an aggressive oxidation process, while the information about the synergistic effect between H3PO4 and H2O2 is quite lack, especially whether some strong oxidant intermediates is existed. In this work, we reported the PHP pretreatment system could self-generate peroxyacetic acid oxidant, which mediated the overall lignocellulose deconstruction, and hemicellulose/lignin degradation. Results The PHP pretreatment profile on wheat straw and corn stalk were investigated. The pathways/mechanisms of peroxyacetic acid mediated-PHP pretreatment were elucidated through tracing the structural changes of each component. Results showed that hemicellulose was almost completely solubilized and removed, corresponding to about 87.0% cellulose recovery with high digestibility. Rather high degrees of delignification of 83.5% and 90.0% were achieved for wheat straw and corn stalk, respectively, with the aid of peroxyacetic acid oxidation. A clearly positive correlation was found between the concentration of peroxyacetic acid and the extent of lignocellulose deconstruction. Peroxyacetic acid was mainly self-generated through H2O2 oxidation of acetic acid that was produced from hemicellulose deacetylation and lignin degradation. The self-generated peroxyacetic acid then further contributed to lignocellulose deconstruction and delignification. Conclusions The synergistic effect of H3PO4 and H2O2 in the PHP solvent system could efficiently deconstruct wheat straw and corn stalk lignocellulose through an oxidation-mediated process. The main function of H3PO4 was to deconstruct biomass recalcitrance and degrade hemicellulose through acid hydrolysis, while the function of H2O2 was to facilitate the formation of peroxyacetic acid. Peroxyacetic acid with stronger oxidation ability was generated through the reaction between H2O2 and acetic acid, which was released from xylan and lignin oxidation/degradation. This work elucidated the generation and function of peroxyacetic acid in the PHP pretreatment system, and also provide useful information to tailor peroxide-involved pretreatment routes, especially at acidic conditions. Graphical abstract


2016 ◽  
Vol 14 (1) ◽  
pp. 393-403 ◽  
Author(s):  
Eugenia Koutsouri ◽  
Christiana A. Mitsopoulou

AbstractHerein, we report on the homogeneous photocatalytic evolution of hydrogen by using as reductive catalysts the prismatic symmetric tris – dithiolene complexes of the tungsten, namely [W{S2C2(Ph)2}3] (1) and its monoanion [W{S2C2(Ph)2}3](TBA) (2). Complex 2 is fully characterized by elemental analysis, ESI-MS, IR, UV-Vis and fluorescence spectrophotometry as well as cyclic voltammetry. The photocatalytic system consists of [ReBr(CO)3(bpy)] as a photosensitizer, triethanolamine as a sacrificial electron donor and acetic acid as the proton source. Although the activity of the photocatalytic system is rather small (TON=18), it indicates that the homoleptic tris dithiolene complexes can act as proton reductive catalysts with their monoanion form to be more active in accordance with the findings for the bis - dithiolene complexes.


2004 ◽  
Vol 2 (1) ◽  
pp. 220-233 ◽  
Author(s):  
Jiří Verner ◽  
Milan Potáček

AbstractAromatic 1,4-diazabuta-1,3-dienes in glacial acetic acid with thiocyanates produce via criss-cross cycloaddition reactions the corresponding perhydroimidazo[4,5-d]imidazole-2,5-dithiones. When a mixture of thiocyanate and cyanate in a proper ratio was reacted together, nonsymmetrical 5-thioxo-perhydroimidazo[4,5-d]imidazole-2-ones were isolated. With cyanates substituted aromatic 1,4-diazabuta-1,3-dienes afforded product of acetic acid addition to primary formed 1,3-dipole intermediate 5-(4-substituted phenylamino)-3-(4-substituted phenyl)-2-oxoimidazolidin-4-yl acetate.


2018 ◽  
Vol 32 (2) ◽  
pp. 1754-1760 ◽  
Author(s):  
Tanawan Chalermsaktrakul ◽  
Yukihiko Matsumura

2020 ◽  
Vol MA2020-01 (49) ◽  
pp. 2735-2735
Author(s):  
Alexander J Kukay ◽  
Ritu Sahore ◽  
William Blake Hawley ◽  
Jianlin Li ◽  
David L. Wood

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