Carbon nanofibers@NiSe core/sheath nanostructures as efficient electrocatalysts for integrating highly selective methanol conversion and less-energy intensive hydrogen production

2019 ◽  
Vol 7 (45) ◽  
pp. 25878-25886 ◽  
Author(s):  
Bin Zhao ◽  
Jian-Wen Liu ◽  
Ya-Ru Yin ◽  
Dan Wu ◽  
Jing-Li Luo ◽  
...  
Keyword(s):  
Energy Consumption ◽  
Hydrogen Production ◽  
Carbon Nanofibers ◽  
Value Added ◽  
Methanol Conversion

In situ synthesized carbon nanofibers@NiSe core/sheath nanostructures act as robust and stable electrocatalysts for highly selective methanol conversion to value-added formate and boosting hydrogen production with less energy consumption.

scholarly journals Understanding Selectivity in CO2 Hydrogenation to Methanol for MoP Nanoparticle Catalysts Using In Situ Techniques

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 143
Author(s):  
Melis S. Duyar ◽  
Alessandro Gallo ◽  
Samuel K. Regli ◽  
Jonathan L. Snider ◽  
Joseph A. Singh ◽  
...  
Keyword(s):  
Formation Rate ◽  
Methanol Conversion ◽  
Transition Metal Catalysts ◽  
Colloidal Synthesis ◽  
X Ray ◽  
In Situ Techniques ◽  
Methanol Formation ◽  
Diffuse Reflectance Infrared ◽  
Formate Intermediate

Molybdenum phosphide (MoP) catalyzes the hydrogenation of CO, CO2, and their mixtures to methanol, and it is investigated as a high-activity catalyst that overcomes deactivation issues (e.g., formate poisoning) faced by conventional transition metal catalysts. MoP as a new catalyst for hydrogenating CO2 to methanol is particularly appealing for the use of CO2 as chemical feedstock. Herein, we use a colloidal synthesis technique that connects the presence of MoP to the formation of methanol from CO2, regardless of the support being used. By conducting a systematic support study, we see that zirconia (ZrO2) has the striking ability to shift the selectivity towards methanol by increasing the rate of methanol conversion by two orders of magnitude compared to other supports, at a CO2 conversion of 1.4% and methanol selectivity of 55.4%. In situ X-ray Absorption Spectroscopy (XAS) and in situ X-ray Diffraction (XRD) indicate that under reaction conditions the catalyst is pure MoP in a partially crystalline phase. Results from Diffuse Reflectance Infrared Fourier Transform Spectroscopy coupled with Temperature Programmed Surface Reaction (DRIFTS-TPSR) point towards a highly reactive monodentate formate intermediate stabilized by the strong interaction of MoP and ZrO2. This study definitively shows that the presence of a MoP phase leads to methanol formation from CO2, regardless of support and that the formate intermediate on MoP governs methanol formation rate.

scholarly journals Computational and experimental investigations of one-step conversion of poly(carbonate)s into value-added poly(aryl ether sulfone)s

2016 ◽  
Vol 113 (28) ◽  
pp. 7722-7726 ◽  
Author(s):  
Gavin O. Jones ◽  
Alexander Yuen ◽  
Rudy J. Wojtecki ◽  
James L. Hedrick ◽  
Jeannette M. García
Keyword(s):  
High Performance ◽  
Density Functional ◽  
Value Added ◽  
Single Step ◽  
Nucleophilic Attack ◽  
Experimental Investigations ◽  
Aryl Ether ◽  
One Step ◽  
Poly Carbonate

It is estimated that ∼2.7 million tons poly(carbonate)s (PCs) are produced annually worldwide. In 2008, retailers pulled products from store shelves after reports of bisphenol A (BPA) leaching from baby bottles, reusable drink bottles, and other retail products. Since PCs are not typically recycled, a need for the repurposing of the PC waste has arisen. We report the one-step synthesis of poly(aryl ether sulfone)s (PSUs) from the depolymerization of PCs and in situ polycondensation with bis(aryl fluorides) in the presence of carbonate salts. PSUs are high-performance engineering thermoplastics that are commonly used for reverse osmosis and water purification membranes, medical equipment, as well as high temperature applications. PSUs generated through this cascade approach were isolated in high purity and yield with the expected thermal properties and represent a procedure for direct conversion of one class of polymer to another in a single step. Computational investigations performed with density functional theory predict that the carbonate salt plays two important catalytic roles in this reaction: it decomposes the PCs by nucleophilic attack, and in the subsequent polyether formation process, it promotes the reaction of phenolate dimers formed in situ with the aryl fluorides present. We envision repurposing poly(BPA carbonate) for the production of value-added polymers.

Ruthenium catalyzed hydrogen production from formaldehyde–water solution

2021 ◽  
Author(s):  
Mahendra Kumar Awasthi ◽  
Sanjay Kumar Singh
Keyword(s):  
Hydrogen Production ◽  
Water Solution ◽  
Ruthenium Catalyst ◽  
Aqueous Formaldehyde

Efficient hydrogen production from aqueous formaldehyde with appreciably high TOF and TON achieved over an in situ generated ruthenium catalyst in water at 95 °C.

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