scholarly journals The role of Praseodymium oxide-Impregnated Clinoptilolite Zeolite Catalyst to Increase Octane Number in Gasoline

2018 ◽  
Vol 67 ◽  
pp. 03051
Author(s):  
Eny Kusrini ◽  
Yan Mulders Togar ◽  
Vino Hasyim ◽  
Anwar Usman

In the present work, the role of praseodymium oxide as a promotor of active site in zeolite base as catalyst for increasing the octance number in gasoline were investigated. In this study, we used three types of catalyst, namely the activated clipnotilolite zeolite (catalyst 1), Pr6O11-impregnated clinoptilolite zeolite 0.01 (w/w%) (catalyst 2) and Pr6O11-impregnated clinoptilolite zeolite 0.1 (w/w%) (catalyst 3). Both catalyst 2 and 3 were prepared by impregnation method. The calcination temperature for all of catalysts was set at 500°C for 2 hours to remove the organic impurities and stabilize the structure of catalyst. The Si/Al ratio increased from 5.1 to 5.85 with prasedymium nitrate hexahydrate percentage in catalysts 2 and 3 were 0.14 and 0.05%, respectively. The surface area of catalysts 1 - 3 are 19.42, 18.09 and 15.22 m2/g, respectively. The activity performance of catalyst 3 with 1 and 3 % loading at 27.7°C for 2 min have increased the octane number of 0.1. Increasing octane number of 0.1 was also confirmed by GC-MS data which showed the presence of decreasing C4-C11 hydrocarbon compounds and increasing of aromatic compounds. Pr6O11-impregnated clinoptilolite zeolite catalyst is potential for application in fuel system to increase octane number at room temperature (27.7°C).

2019 ◽  
Author(s):  
Shuyuan Zheng ◽  
Taiping Hu ◽  
Xin Bin ◽  
Yunzhong Wang ◽  
Yuanping Yi ◽  
...  

Pure organic room temperature phosphorescence (RTP) and luminescence from nonconventional luminophores have gained increasing attention. However, it remains challenging to achieve efficient RTP from unorthodox luminophores, on account of the unsophisticated understanding of the emission mechanism. Here we propose a strategy to realize efficient RTP in nonconventional luminophores through incorporation of lone pairs together with clustering and effective electronic interactions. The former promotes spin-orbit coupling and boost the consequent intersystem crossing, whereas the latter narrows energy gaps and stabilizes the triplets, thus synergistically affording remarkable RTP. Experimental and theoretical results of urea and its derivatives verify the design rationale. Remarkably, RTP from thiourea solids with unprecedentedly high efficiency of up to 24.5% is obtained. Further control experiments testify the crucial role of through-space delocalization on the emission. These results would spur the future fabrication of nonconventional phosphors, and moreover should advance understanding of the underlying emission mechanism.<br>


2007 ◽  
Vol 2 (1) ◽  
Author(s):  
A. Ros ◽  
C. Canals-Batlle ◽  
M.A. Lillo-Ródenas ◽  
E. Fuente ◽  
M. A. Montes-Morán ◽  
...  

This paper focuses on the valorisation of solid residues obtained from the thermal treatment of sewage sludge. In particular, sewage sludge samples were collected from two waste water treatment plants (WWTPs) with different sludge line basic operations. After drying, sludges were heated up to 700 °C in appropriate ovens under diluted air (gasification) and inert (pyrolysis) atmospheres. The solids obtained, as well as the dried (raw) sludges, were characterised to determine their textural properties and chemical composition, including the speciation of their inorganic fraction. All the materials under study were employed as adsorbents/catalysts in H2S removal experiments at room temperature. It was found that, depending on the particular sludge characteristics, outstanding results can be achieved both in terms of retention capacities and selectivity. Some of the solids outperform commercially available sorbents specially designed for gaseous emissions control. In these adsorbents/catalysts, H2S is selectively oxidised to elemental sulphur most likely due to the presence of inorganic, catalytically active species. The role of the carbon-enriched part on these solids is also remarked.


2020 ◽  
Vol 281 ◽  
pp. 121028 ◽  
Author(s):  
Saad Mabrouk Yakout ◽  
Hanan A. Mousa ◽  
Hala T. Handal ◽  
Walid Sharmoukh

Nanoscale ◽  
2015 ◽  
Vol 7 (35) ◽  
pp. 14643-14651 ◽  
Author(s):  
Shuang Xu ◽  
Jun Gao ◽  
Linlin Wang ◽  
Kan Kan ◽  
Yu Xie ◽  
...  

2011 ◽  
Vol 678 ◽  
pp. 75-84 ◽  
Author(s):  
Marcello Cabibbo

Magnesium alloys containing rare earth elements are known to have high specific strength and corrosion resistance. The addition of SiC ceramic particles makes the metal matrix composite stronger with better wear and creep resistance and a still good machinability. The role of the reinforcement particles to the enhanced strength can be quantitatively evaluated using transmission electron microscopy (TEM). This paper presents a quantitative strengthening evaluation in a SiC Mg-RE composite alloy. The different contributions were determined by TEM inspections. The microstructure strengthening mechanism was studied after room temperature compression specimens. The way of combining the different contributions and the comparison to the measured yield stress, is also discussed and justified.


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