Kinetics and Mechanism of H2O2 Direct Synthesis over a Pd/C Catalyst in a Batch Reactor

2012 ◽  
Vol 51 (26) ◽  
pp. 8903-8912 ◽  
Author(s):  
Pierdomenico Biasi ◽  
Nicola Gemo ◽  
José Rafael Hernández Carucci ◽  
Kari Eränen ◽  
Paolo Canu ◽  
...  
2013 ◽  
Vol 56 (9-10) ◽  
pp. 540-549 ◽  
Author(s):  
Nicola Gemo ◽  
Pierdomenico Biasi ◽  
Paolo Canu ◽  
Federica Menegazzo ◽  
Francesco Pinna ◽  
...  

2013 ◽  
Vol 3 (11) ◽  
pp. 2971 ◽  
Author(s):  
Tatsumi Ishihara ◽  
Kohei Shigeta ◽  
Yuuki Ooishi ◽  
Maki Matsuka ◽  
Hidehisa Hagiwara ◽  
...  

2020 ◽  
Vol 5 (2) ◽  
pp. 46-55
Author(s):  
Mawan Nugraha ◽  
◽  
Susiani Pupon ◽  
Nofiandri Setyasmara ◽  
◽  
...  

Hydrogen peroxide is an important material for bleaching agent in paper production related to the low price and environmentally friendly chemical. The current production of H2O2 is well-known as indirect synthesis, which uses danger anthraquinone. The synthesis was improved by using the direct reaction of H2 and O2 on Pd or PdAu alloy's catalyst surface and has been known as direct synthesis. The current catalyst used is Pd-Au, but it has limited availability in nature. Therefore we need the alternative of Pd-Au. We investigated Ni alloyed with Pd for the new H2O2 direct synthesis catalyst using a density functional theory approach. We selected the O adsorption to screen the catalysts and compared the species adsorption trend on the surfaces of PdNi and the proven catalysts such as Pd, PdAu, and PdHg. Since the trend of O adsorption on the PdAu and PdNi is similar, it can be concluded that the catalytic selectivity of PdNi equal with PdAu. Further, the stability of PdNi alloy was explored by calculating the binding and compared it with Pd, which leads to the conclusion that PdNi can be a good catalyst for H2O2 synthesis.


Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 949
Author(s):  
Lucas Warmuth ◽  
Gülperi Nails ◽  
Maria Casapu ◽  
Sheng Wang ◽  
Silke Behrens ◽  
...  

Titania nanotubes (TNTs) impregnated with Pd and Pt nanoparticles are evaluated as heterogeneous catalysts in different conditions in two reactions: catalytic CO oxidation (gas phase, up to 500 °C) and H2O2 direct synthesis (liquid phase, 30 °C). The TNTs are obtained via oxidation of titanium metal and the intermediate layer-type sodium titanate Na2Ti3O7. Thereafter, the titanate layers are exfoliated and show self-rolling to TNTs, which, finally, are impregnated with Pd or Pt nanoparticles at room temperature by using Pd(ac)2 and Pt(ac)2. The resulting crystalline Pd/TNTs and Pt/TNTs are realized with different lengths (long TNTs: 2.0–2.5 µm, short TNTs: 0.23–0.27 µm) and a specific surface area up to 390 m2/g. The deposited Pd and Pt particles are 2–5 nm in diameter. The TNT-derived catalysts show good thermal (up to 500 °C) and chemical stability (in liquid-phase and gas-phase reactions). The catalytic evaluation results in a low CO oxidation light-out temperature of 150 °C for Pt/TNTs (1 wt-%) and promising H2O2 generation with a productivity of 3240 molH2O2 kgPd−1 h−1 (Pd/TNTs, 5 wt-%, 30 °C). Despite their smaller surface area, long TNTs outperform short TNTs with regard to both CO oxidation and H2O2 formation.


2011 ◽  
Vol 176-177 ◽  
pp. 172-177 ◽  
Author(s):  
Pierdomenico Biasi ◽  
Federica Menegazzo ◽  
Francesco Pinna ◽  
Kari Eränen ◽  
Tapio O. Salmi ◽  
...  

2007 ◽  
Vol 119 ◽  
pp. 287-290 ◽  
Author(s):  
Kyung Won La ◽  
Min Hye Youn ◽  
Jin Suk Chung ◽  
Sung Hyeon Baeck ◽  
In Kyu Song

CexTi1-xO2 and H3PW12O40/CexTi1-xO2 catalysts were prepared by sol-gel method, and they were applied to the direct synthesis of dimethyl carbonate (DMC) from methanol and carbon dioxide in a batch reactor. The reaction was carried out in an autoclave reactor at 170oC and 5 MPa. It was found that CexTi1-xO2 exhibited a higher catalytic performance than pure CeO2 and TiO2. The catalytic performance of CexTi1-xO2 was the maximum when x=0.1. It was also revealed that H3PW12O40/CexTi1-xO2 catalysts showed a remarkably enhanced catalytic performance than the corresponding CexTi1-xO2 catalysts. The amount of DMC produced by 15 wt% H3PW12O40/ Ce0.1Ti0.9O2 catalyst was six times higher than that produced by Ce0.1Ti0.9O2 catalyst. It is concluded that both Brönsted acid sites provided by H3PW12O40 and base sites in CexTi1-xO2 played an important role in improving the catalytic performance of H3PW12O40/CexTi1-xO2.


2015 ◽  
Vol 248 ◽  
pp. 108-114 ◽  
Author(s):  
Tapio Salmi ◽  
Nicola Gemo ◽  
Pierdomenico Biasi ◽  
Juan Garcia Serna

2007 ◽  
Vol 62 (3-4) ◽  
pp. 305-307 ◽  
Author(s):  
Alena Komersová ◽  
Markéta Masopustová ◽  
Karel Komers ◽  
Šárka Štěpánková ◽  
Alexandr Čegan

Abstract Kinetics and mechanism of in vitro hydrolyses of acetylcholine and acetylthiocholine by carbamates were studied in a batch reactor at 25 °C, pH 8, and ionic strength of 0.11 m. Every hydrolysis was monitored by 3-4 independent methods. All studied hydrolyses can be described by the model of competitive inhibition with an irreversible step (k3). A table of obtained average values of rate constants and discussion of the resultes are given.


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