Size-dependent CO and propylene oxidation activities of platinum nanoparticles on the monolithic Pt/TiO2–YOxdiesel oxidation catalyst under simulative diesel exhaust conditions

2015 ◽  
Vol 5 (4) ◽  
pp. 2358-2365 ◽  
Author(s):  
Zhengzheng Yang ◽  
Jun Li ◽  
Hailong Zhang ◽  
Yi Yang ◽  
Maochu Gong ◽  
...  

Small platinum oxide particles are beneficial for forming Pt0active species under diesel exhaust conditions, hence showing better DOC reactivity.

2020 ◽  
Vol 34 (12) ◽  
pp. 16542-16551
Author(s):  
Jian Wang ◽  
He Liu ◽  
Shiguang Fan ◽  
Weining Li ◽  
Zhuo Li ◽  
...  

1966 ◽  
Vol 19 (4) ◽  
pp. 529 ◽  
Author(s):  
IT Ernst ◽  
JL Garnett ◽  
WA Sollich-Baumgartner

The formation of paramagnetic species on catalyst surfaces at room temperature through the interaction of polynuclear aromatics in solid, liquid, or solute form with hydrated platinum oxide (PtO2,2H2O) is reported. The results are attributed to the formation of charge-transfer complexes, where the transferred electrons couple weakly, forming essentially a "diradicaloid" complex with a low-lying, thermally populated, triplet state. The effect of solvent, particle size, oxygen, water of crystallization, and temperature on the generation and stability of these e.s.r. active species has been investigated. The possible importance of these paramagnetic species in catalytic self-activation and hydrogen exchange reactions has been discussed. The following Group VIII transition metal oxides gave no e.s.r. spectra under relatively severe reaction conditions such as 1 hr at 120�: PdO; Ru02,2H20; RuO2; Rh2O3; IrO2,2H2O; ReO2; and NiO.


1995 ◽  
Vol 268 (1) ◽  
pp. R85-R91 ◽  
Author(s):  
G. A. Gronert ◽  
D. L. Fung ◽  
J. H. Jones ◽  
S. L. Shafer ◽  
S. V. Hildebrand ◽  
...  

We investigated the effects of body size on the pharmacokinetics and pharmacodynamics of the renally cleared muscle relaxant metocurine. We hypothesized that pharmacokinetics of the drug would change allometrically in proportion to physiological time [infinity Mb0.25, where Mb is body mass] and that pharmacodynamics would be independent of size because of the highly conserved structure of the acetylcholine receptor. Metocurine effects during general anesthesia were examined in 17 rats, 8 cats, 6 dogs, 5 pigs, 7 sheep, and 12 horses. Allometric analysis demonstrated size dependence for pharmacokinetics, which were affected by physiological time (Mb0.25). Pharmacodynamics were size independent, except for the value for effect compartment concentration associated with 50% twitch paralysis (IC50). Data from individual species had a bimodal distribution that was significant: pigs and sheep were more sensitive than other large species, and their IC50 appeared size independent. IC50 was size dependent in more active species (horse, dog, cat, rat). Although the mechanism is unknown, we speculate that this trend might relate to receptor density within the end plate. Thus pharmacokinetics changed in proportion to physiological time, and pharmacodynamics were in part size independent.


2013 ◽  
Vol 7 (S6) ◽  
Author(s):  
Hidekazu Nakanishi ◽  
Takeki Hamasaki ◽  
Tomoya Kinjo ◽  
Kiichiro Teruya ◽  
Shigeru Kabayama ◽  
...  

2012 ◽  
Author(s):  
Keita Ishizaki ◽  
Naoki Mitsuda ◽  
Naoki Ohya ◽  
Hiroshi Ohno ◽  
Takahiro Naka ◽  
...  

ACS Catalysis ◽  
2016 ◽  
Vol 6 (9) ◽  
pp. 6151-6155 ◽  
Author(s):  
Suresh Gatla ◽  
Daniel Aubert ◽  
Giovanni Agostini ◽  
Olivier Mathon ◽  
Sakura Pascarelli ◽  
...  

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