Carbon nitride supported AgPd alloy nanocatalysts for dehydrogenation of formic acid under visible light

2017 ◽  
Vol 5 (14) ◽  
pp. 6382-6387 ◽  
Author(s):  
Liping Xiao ◽  
Young-Si Jun ◽  
Binghui Wu ◽  
Deyu Liu ◽  
Tracy T Chuong ◽  
...  
Keyword(s):  
Formic Acid ◽  
Visible Light ◽  
Carbon Nitride ◽  
Room Temperature ◽  
Ambient Condition ◽  
Alloy Nanoparticles ◽  
Highly Active ◽  
One Step ◽  
The One ◽  
Temperature Preparation

We report a facile approach for the one-step room-temperature preparation of nearly monodisperse AgPd alloy nanoparticles supported on semiconductor graphitic carbon nitride (g-CN). The AgPd/g-CN nanocatalysts are highly active and durable for dehydrogenation of formic acid under visible light or dark at ambient condition.

Hydrogen production from formic acid solution by modified TiO2 and titanate nanotubes in a two-step system under visible light irradiation

2014 ◽  
Vol 69 (8) ◽  
pp. 1676-1681 ◽  
Author(s):  
H. M. Yeh ◽  
S. L. Lo ◽  
M. J. Chen ◽  
H. Y. Chen
Keyword(s):  
Hydrogen Production ◽  
Formic Acid ◽  
Visible Light ◽  
Renewable Energy Sources ◽  
Hydrogen Gas ◽  
Titanate Nanotubes ◽  
Formic Acid Solution ◽  
One Step ◽  
The One ◽  
Platinum Loading

Hydrogen gas is one of the most promising renewable energy sources, and the final product of hydrogen combustion is nothing but water. However, it is still a big challenge to produce hydrogen and store it. Many studies have been conducted into produce hydrogen from water using photocatalysts. Z-scheme photocatalysis is a two-photocatalyst system that comprises a hydrogen catalyst and an oxygen catalyst to produce hydrogen and oxygen respectively. Compared to the one-step system, the two-step system can promote the efficiency of water splitting. In addition, formic acid (FA) is a convenient hydrogen-storage material and can be safely handled in aqueous solutions. Therefore, this study investigated the photocatalytic conversion of FA solution to hydrogen using visible light with several types of hydrogen catalysts (CdS/titanate nanotubes (TNTs), CdS/TiO2, Pt/CdS/TNTs) and WO3 as the oxygen catalyst. The results showed that the yield of hydrogen with CdS/TNTs + WO3 was much higher than with CdS/TiO2 + WO3. Moreover, coating the photocatalysts with metal could further promote the reaction. The optimal platinum loading was 0.01 wt%, and the hydrogen production achieved was 852.5 μmol · h−1 with 20 vol% FA solution.

A Study on the Rearrangement of Dialkyl 1-Aryl-1-hydroxymethylphosphonates to Benzyl Phosphates

2020 ◽  
Vol 24 (4) ◽  
pp. 465-471 ◽  
Author(s):  
Zita Rádai ◽  
Réka Szabó ◽  
Áron Szigetvári ◽  
Nóra Zsuzsa Kiss ◽  
Zoltán Mucsi ◽  
...  
Keyword(s):  
Quantum Chemical ◽  
Room Temperature ◽  
Phase Transfer ◽  
One Pot ◽  
Substrate Dependence ◽  
Triethylbenzylammonium Chloride ◽  
One Step ◽  
The Pudovik Reaction ◽  
The One ◽  
Solid Liquid

The phospha-Brook rearrangement of dialkyl 1-aryl-1-hydroxymethylphosphonates (HPs) to the corresponding benzyl phosphates (BPs) has been elaborated under solid-liquid phase transfer catalytic conditions. The best procedure involved the use of triethylbenzylammonium chloride as the catalyst and Cs2CO3 as the base in acetonitrile as the solvent at room temperature. The substrate dependence of the rearrangement has been studied, and the mechanism of the transformation under discussion was explored by quantum chemical calculations. The key intermediate is an oxaphosphirane. The one-pot version starting with the Pudovik reaction has also been developed. The conditions of this tandem transformation were the same, as those for the one-step HP→BP conversion.

Study of Antioxidant Property of the Rhizome Extract of Polygonatum cirrhifolium (Mahameda) and its use in the green synthesis of Gold nanoparticles

2017 ◽  
Vol 1 (2) ◽  
Author(s):  
Braja Gopal Bag ◽  
Shib Shankar Dash ◽  
Anup Mandal
Keyword(s):  
Gold Nanoparticles ◽  
Green Synthesis ◽  
Room Temperature ◽  
Chemical Constituents ◽  
Antioxidant Property ◽  
Dpph Radical ◽  
Mild Conditions ◽  
One Step ◽  
The One

The antioxidant efficacy of the rhizome extract of Polygonatum cirrhifolium (Mahameda) has been studied against a stable 2, 2-diphenylpicrylhydrazyl (DPPH) radical at room temperature. The chemical constituents present in the rhizome extract have been utilized for the one step synthesis of stable gold nanoparticles at room temperature under very mild conditions.

scholarly journals Improving the Activity of Fe/C/N ORR Electrocatalyst Using Double Ammonia Promoted CO2 Laser Pyrolysis

2020 ◽  
Vol 6 (4) ◽  
pp. 63
Author(s):  
Henri Perez ◽  
Mathieu Frégnaux ◽  
Emeline Charon ◽  
Arnaud Etcheberry ◽  
Olivier Sublemontier
Keyword(s):  
Co2 Laser ◽  
Large Scale ◽  
Laser Energy ◽  
Reduction Reaction ◽  
Laser Pyrolysis ◽  
Highly Active ◽  
One Step ◽  
Orr Activity ◽  
Set Up ◽  
The One

Recently, we reported the use of CO2 laser pyrolysis for the synthesis of promising Fe/C/N electrocatalysts for Oxygen Reduction Reaction (ORR) in fuel cells. The set-up used single laser pyrolysis of an aerosolized solution of iron acetylacetonate in toluene with ammonia, both as laser energy transfer agent and nitrogen source. In the present paper, we investigate the effect of a second ammonia promoted CO2 laser pyrolysis on the feature and ORR activity of Fe/C/N electrocatalysts. Indeed, compared to single pyrolysis, the second ammonia promoted CO2 laser pyrolysis could be an interesting way to synthesize in one-step performing ORR electrocatalysts on a large scale. For this comparison, a two-stage reactor was built, allowing both single ammonia-induced CO2 laser pyrolysis as reported previously or double ammonia-induced CO2 laser pyrolysis. In the latter configuration, the catalyst nanopowder flow is formed at the first stage of the reactor, then mixed with a second ammonia flow and allowed to cross a second CO2 laser beam, thus undergoing a second ammonia-induced CO2 laser pyrolysis before being collected on filters. It is found that the second ammonia-induced CO2 laser pyrolysis significantly improves the ORR performances of the materials prepared by single CO2 laser pyrolysis. The effect is demonstrated for three different catalysts for which the onset potentials for the ORR from single-stage to double-stage configuration increase from 625 mV to 845 mV, 790 mV to 860 mV, and 800 mV to 885 mV, respectively. The selectivity of the ORR was determined at 600 mV/SHE and lie between 3.41 and 3.72. These promising performances suggesting potentialities for the one-step formation of highly active Fe/C/N ORR electrocatalysts are discussed, based on results of surface analysis by XPS, specific surface area measurements, and Raman spectroscopy.

scholarly journals Characterization of highly active 2-keto-3-deoxy-L-arabinonate and 2-keto-3-deoxy-D-xylonate dehydratases in terms of the biotransformation of hemicellulose sugars to chemicals

2020 ◽  
Vol 104 (16) ◽  
pp. 7023-7035
Author(s):  
Samuel Sutiono ◽  
Bettina Siebers ◽  
Volker Sieber
Keyword(s):  
Racemic Mixture ◽  
Highly Active ◽  
Key Points ◽  
Deoxy Sugar ◽  
Weimberg Pathway ◽  
One Step ◽  
The One ◽  
Increased Activity ◽  
Enzyme Class

Abstract2-keto-3-L-arabinonate dehydratase (L-KdpD) and 2-keto-3-D-xylonate dehydratase (D-KdpD) are the third enzymes in the Weimberg pathway catalyzing the dehydration of respective 2-keto-3-deoxy sugar acids (KDP) to α-ketoglutaric semialdehyde (KGSA). The Weimberg pathway has been explored recently with respect to the synthesis of chemicals from L-arabinose and D-xylose. However, only limited work has been done toward characterizing these two enzymes. In this work, several new L-KdpDs and D-KdpDs were cloned and heterologously expressed in Escherichia coli. Following kinetic characterizations and kinetic stability studies, the L-KdpD from Cupriavidus necator (CnL-KdpD) and D-KdpD from Pseudomonas putida (PpD-KdpD) appeared to be the most promising variants from each enzyme class. Magnesium had no effect on CnL-KdpD, whereas increased activity and stability were observed for PpD-KdpD in the presence of Mg2+. Furthermore, CnL-KdpD was not inhibited in the presence of L-arabinose and L-arabinonate, whereas PpD-KdpD was inhibited with D-xylonate (I50 of 75 mM), but not with D-xylose. Both enzymes were shown to be highly active in the one-step conversions of L-KDP and D-KDP. CnL-KdpD converted > 95% of 500 mM L-KDP to KGSA in the first 2 h while PpD-KdpD converted > 90% of 500 mM D-KDP after 4 h. Both enzymes in combination were able to convert 83% of a racemic mixture of D,L-KDP (500 mM) after 4 h, with both enzymes being specific toward the respective stereoisomer. Key points• L-KdpDs and D-KdpDs are specific toward L- and D-KDP, respectively.• Mg2+affected activity and stabilities of D-KdpDs, but not of L-KdpDs.• CnL-KdpD and PpD-KdpD converted 0.5 M of each KDP isomer reaching 95 and 90% yield.• Both enzymes in combination converted 0.5 M racemic D,L-KDP reaching 83% yield.

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