scholarly journals Anchoring carbon nanotubes and post-hydroxylation treatment enhanced Ni nanofiber catalysts towards efficient hydrous hydrazine decomposition for effective hydrogen generation

2019 ◽  
Vol 55 (61) ◽  
pp. 9011-9014 ◽  
Author(s):  
Pan Yang ◽  
Lijun Yang ◽  
Qiang Gao ◽  
Qiang Luo ◽  
Xiaochong Zhao ◽  
...  
Keyword(s):  
Activation Energy ◽  
Carbon Nanotubes ◽  
Hydrogen Generation ◽  
Hydrazine Decomposition ◽  
Effective Hydrogen

CNTs and hydroxylation enhanced Ni nanofibers for decomposing hydrous hydrazine with a reduced activation energy down to 51.05 kJ mol−1.

Retracted Article: Mesoporous multiwalled carbon nanotubes as supports for monodispersed iron–boron catalysts: improved hydrogen generation from hydrous hydrazine decomposition

2013 ◽  
Vol 1 (2) ◽  
pp. 358-366 ◽  
Author(s):  
Dong Ge Tong ◽  
Wei Chu ◽  
Ping Wu ◽  
Gui Fang Gu ◽  
Li Zhang
Keyword(s):  
Carbon Nanotubes ◽  
Carbon Nanotube ◽  
Multiwalled Carbon Nanotubes ◽  
Hydrogen Generation ◽  
Multiwalled Carbon Nanotube ◽  
Multiwalled Carbon ◽  
Hydrazine Decomposition ◽  
Retracted Article

Mesoporous multiwalled carbon nanotube supported monodispersed iron–boron catalysts greatly enhanced the hydrogen generation from hydrous hydrazine decomposition.

scholarly journals Retraction: Mesoporous multiwalled carbon nanotubes as supports for monodispersed iron–boron catalysts: improved hydrogen generation from hydrous hydrazine decomposition

2020 ◽  
Vol 8 (14) ◽  
pp. 6908-6908
Author(s):  
Dong Ge Tong
Keyword(s):  
Carbon Nanotubes ◽  
Multiwalled Carbon Nanotubes ◽  
Hydrogen Generation ◽  
Multiwalled Carbon ◽  
Hydrazine Decomposition

Retraction of ‘Mesoporous multiwalled carbon nanotubes as supports for monodispersed iron–boron catalysts: improved hydrogen generation from hydrous hydrazine decomposition’ by Dong Ge Tong et al., J. Mater. Chem. A, 2013, 1, 358–366.

Increased crystallinity of RuSe2/Carbon Nanotubes for enhanced electrochemical hydrogen generation performance

Nanoscale ◽  
2021 ◽  
Author(s):  
Dongze Li ◽  
Meng Zha ◽  
Ligang Feng ◽  
Guangzhi Hu ◽  
Chaoquan Hu ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Water Splitting ◽  
Hydrogen Generation ◽  
Electrochemical Water Splitting

Ru-based catalyst is significant in the green hydrogen generation via electrochemical water-splitting reaction. Herein, it is found that the increased crystallinity of cubic RuSe2 nanoparticles anchored over carbon nanotubes (RuSe2/CNTs)...

In situ synthesis of Ni nanofibers via vacuum thermal reduction and their efficient catalytic properties for hydrogen generation

2018 ◽  
Vol 6 (24) ◽  
pp. 11370-11376 ◽  
Author(s):  
Qinglong Fu ◽  
Pan Yang ◽  
Jingchuan Wang ◽  
Hefang Wang ◽  
Lijun Yang ◽  
...  
Keyword(s):  
Reduction Method ◽  
Hydrogen Generation ◽  
Catalytic Properties ◽  
Decomposition Reaction ◽  
Thermal Reduction ◽  
In Situ Synthesis ◽  
Hydrazine Decomposition

Ni nanofibers have been prepared by a vacuum thermal reduction method, and further used as efficient catalysts for hydrogen generation from hydrous hydrazine decomposition reaction.

scholarly journals Mechanistic study of hydrazine decomposition on Ir(111)

2020 ◽  
Vol 22 (7) ◽  
pp. 3883-3896 ◽  
Author(s):  
Xiuyuan Lu ◽  
Samantha Francis ◽  
Davide Motta ◽  
Nikolaos Dimitratos ◽  
Alberto Roldan
Keyword(s):  
Hydrogen Generation ◽  
Mechanistic Study ◽  
Hydrazine Decomposition

Theory–experiment evidence of continuous hydrogen generation upon N–N splitting and NH2 assisted dehydrogenation of N2H4 catalysed by metallic Ir(111) catalyst.

PVP Stabilized Ruthenium (0) Nanorods as Effective Catalysts in Hydrogen Generation from the Hydrolysis of Sodium Borohydride

2011 ◽  
Vol 197-198 ◽  
pp. 1577-1581 ◽  
Author(s):  
Shu Ge Peng ◽  
Jun Na Liu ◽  
Xiao Fei Liu ◽  
Yu Qing Zhang ◽  
Jun Zhang
Keyword(s):  
Activation Energy ◽  
Microwave Heating ◽  
Absorption Spectra ◽  
Catalytic Property ◽  
Sodium Borohydride ◽  
Boiling Point ◽  
Hydrogen Generation ◽  
First Time ◽  
Hydrolysis Of

Poly (N-vinyl-2-pyrrolidone) (PVP) - stabilized ruthenium (0) nanorods have been successfully synthesized by refluxing ruthenium (Ⅲ) chloride (RuCl3) in low boiling point alcohols (including ethanol, n-propanol, and n-butanol) using microwave heating for the first time. The effects of low boiling point alcohols on the preparation and catalytic property of ruthenium nanorods were discussed. UV-Vis absorption spectra indicated ruthenium nanorods could be synthesized in n-butanol after 2 h refluxing, far below the refluxing time in ethanol and n-propanol. The activation energy of the hydrolysis of NaBH4 catalyzed by Ruthenium (0) nanorods obtained in ethanol, n-propanol, and n-butanol were determined to be 41.1, 33.3, and 27.9 kJ / mol, respectively.

Hydrogen generation from hydrazine catalyzed by a Ni1-(CeO1.8)0.5/carbon-nanotubes catalyst

2018 ◽  
Vol 126 (1) ◽  
pp. 153-165 ◽  
Author(s):  
Yongli Dong ◽  
Hong-Yu Zhang ◽  
Guohui Yin ◽  
Jiquan Zhao ◽  
Yuecheng Zhang
Keyword(s):  
Carbon Nanotubes ◽  
Hydrogen Generation

Oxidation of dibenzothiophene using the heterogeneous catalyst of tungsten-based carbon nanotubes

2019 ◽  
Vol 8 (1) ◽  
pp. 68-77 ◽  
Author(s):  
Nguyen Duc Vu Quyen ◽  
Tran Ngoc Tuyen ◽  
Dinh Quang Khieu ◽  
Ho Van Minh Hai ◽  
Dang Xuan Tin ◽  
...  
Keyword(s):  
Activation Energy ◽  
Carbon Nanotubes ◽  
Heterogeneous Catalyst ◽  
Activation Enthalpy ◽  
Intermediate Compound ◽  
Activation Process ◽  
Modern Methods ◽  
The Stability ◽  
Reaction Cycles ◽  
Mechanism Of The Reaction

Abstract Highly effective tungsten-based carbon nanotubes (W/CNT) were synthesized and used as a heterogeneous catalyst for the oxidation of dibenzothiophene (DBT) with the oxidant H2O2. The obtained materials were characterized by modern methods. The Langmuir–Hinshelwood kinetics model described the precursor mechanism of the reaction well through an intermediate compound. The low activation energy showed that the reaction was mainly controlled by diffusion. The positive activation enthalpy proved the endothermic nature of the activation process, and this process did not alter the inside structure of the catalyst. The thermodynamic parameters of the reaction were determined, which implied that the oxidation was endothermic and spontaneous at 303 K. The more negative values of the Gibbs free energy from 283 to 323 K confirmed that the reaction was more favorable at high temperatures. The stability and activity of catalyst were retained after three reaction cycles.

Sign in / Sign up

Export Citation Format

Share Document