The effect of a vitamin B12 based catalyst on hydrogen peroxide oxidation reactions and the performance evaluation of a membraneless hydrogen peroxide fuel cell under physiological pH conditions

2020 ◽  
Vol 8 (8) ◽  
pp. 2749-2755 ◽  
Author(s):  
Jungyeon Ji ◽  
Yongjin Chung ◽  
Yongchai Kwon
Keyword(s):  
Hydrogen Peroxide ◽  
Performance Evaluation ◽  
Fuel Cell ◽  
Vitamin B12 ◽  
Oxidation Reaction ◽  
Oxidation Reactions ◽  
Peroxide Oxidation ◽  
Hydrogen Peroxide Oxidation ◽  
Ph Conditions ◽  
Anodic Catalyst

A new anodic catalyst (CNT/VitB12) is introduced for promoting the hydrogen peroxide oxidation reaction (HPOR) and the performance of a membraneless hydrogen peroxide fuel cell (HPFC).

scholarly journals Hydrogen Peroxide Oxidation Reaction on a 4-Mercaptopyridine Self-Assembled Monolayer on Au(111) Metallized by Platinum Nanoislands

2021 ◽  
Author(s):  
Mathias Piescheck ◽  
Areeg Abdelrahman ◽  
Johannes M. Hermann ◽  
Heiko Müller ◽  
Timo Jacob ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Oxidation Reaction ◽  
Structural Changes ◽  
Systematic Investigation ◽  
Peroxide Oxidation ◽  
Self Assembled Monolayer ◽  
Hydrogen Peroxide Oxidation ◽  
Before And After ◽  
Total Current Density ◽  
Self Assembled

AbstractA systematic investigation of the hydrogen peroxide oxidation reaction (HPOR) in phosphate buffer (pH = 7.3) on an Au(111) single crystal modified with a 4-mercaptopyridine self-assembled monolayer (SAM) has been conducted before and after metallization with Pt. While bare Au(111) shows considerable electrocatalytic activity towards the HPOR, the inhibition of the oxidation reaction after modification with the SAM implies that adsorbed 4-mercaptopyridine molecules do not catalyze the HPOR. However, SAM-modified Au(111) recovers catalytic activity for the HPOR already after a single metallization step fabricating Pt islands on-top. Hydrogen peroxide (HP) may then either react at the (non-metallic) Pt nanoislands or on reactivated Au sites, made accessible by structural changes of the SAM induced by the metallization. The shape of the voltammetric profiles for the HPOR on repeatedly metallized SAMs suggests that the contribution of Au to the total current density gradually diminishes with increasing Pt coverage while the contribution of the Pt islands increases. The electrochemical behavior is dominated by the Pt islands at a coverage of 0.5 ML obtained by three subsequent metallization steps. Graphical abstract

Crystal and solution structure of (E)-1,2-bis(ethylsulphonyl)cyclobutane-1,2-dicarbonitrile

1989 ◽  
Vol 54 (12) ◽  
pp. 3253-3259
Author(s):  
Jaroslav Podlaha ◽  
Miloš Buděšínský ◽  
Jana Podlahová ◽  
Jindřich Hašek
Keyword(s):  
Hydrogen Peroxide ◽  
Solution Structure ◽  
Peroxide Oxidation ◽  
X Ray ◽  
X Ray Crystallography ◽  
Nmr Study ◽  
Hydrogen Peroxide Oxidation ◽  
Unusual Product ◽  
C Nmr

The unusual product of the reaction of 2-chloroacrylonitrile with ethane thiol and following hydrogen peroxide oxidation was found to be (E)-1,2-bis(ethylsulphonyl)cyclobutane-1,2-dicarbonitrile by means of X-ray crystallography. 1H and 13C NMR study of this compound has proven the same conformation of the molecule in solution.

scholarly journals Hydrogen Peroxide Oxidation of Coordinated Thiocyanate Ion in cis- and trans-[Coen2NH3NCS]2+: The Preparation and Properties of trans-[Coen2NH3CN]2+

1973 ◽  
Vol 51 (24) ◽  
pp. 4152-4158 ◽  
Author(s):  
Albert Richard Norris ◽  
James William Lennox Wilson
Keyword(s):  
Hydrogen Peroxide ◽  
Spectral Properties ◽  
Peroxide Oxidation ◽  
Reaction Conditions ◽  
Thiocyanate Ion ◽  
Hydrogen Peroxide Oxidation ◽  
Percent Conversion ◽  
Cis And Trans ◽  
In Cis

The hydrogen peroxide oxidation of thiocyanate ion in cis- and trans-[Coen2NH3NCS]2+ leads to the formation of the corresponding cis- and trans-cyanoammine- and diamminebis(ethylenediamine)cobalt-(III) complexes. The spectral properties of the previously unreported trans-[Coe2NH3CN]2+ are reported and compared to the spectral properties of the cis-isomer.Observations are made concerning the reaction conditions which favor a high percent conversion of trans-[Coen2NH3NCS]2+ to trans-[Coen2NH3CN]2+.

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