scholarly journals Dehydrogenation of Propane to Propylene Using Promoter-Free Hierarchical Pt/Silicalite-1 Nanosheets

Catalysts ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 174 ◽  
Author(s):  
Wannaruedee Wannapakdee ◽  
Thittaya Yutthalekha ◽  
Pannida Dugkhuntod ◽  
Kamonlatth Rodponthukwaji ◽  
Anawat Thivasasith ◽  
...  

Propane dehydrogenation (PDH) is the extensive pathway to produce propylene, which is as a very important chemical building block for the chemical industry. Various catalysts have been developed to increase the propylene yield over recent decades; however, an active site of monometallic Pt nanoparticles prevents them from achieving this, due to the interferences of side-reactions. In this context, we describe the use of promoter-free hierarchical Pt/silicalite-1 nanosheets in the PDH application. The Pt dispersion on weakly acidic supports can be improved due to an increase in the metal-support interaction of ultra-small metal nanoparticles and silanol defect sites of hierarchical structures. This behavior leads to highly selective propylene production, with more than 95% of propylene selectivity, due to the complete suppression of the side catalytic cracking. Moreover, the oligomerization as a side reaction is prevented in the presence of hierarchical structures due to the shortening of the diffusion path length.

2019 ◽  
Author(s):  
Alexander Giovannitti ◽  
Reem B. Rashid ◽  
Quentin Thiburce ◽  
Bryan D. Paulsen ◽  
Camila Cendra ◽  
...  

<p>Avoiding faradaic side reactions during the operation of electrochemical devices is important to enhance the device stability, to achieve low power consumption, and to prevent the formation of reactive side‑products. This is particularly important for bioelectronic devices which are designed to operate in biological systems. While redox‑active materials based on conducting and semiconducting polymers represent an exciting class of materials for bioelectronic devices, they are susceptible to electrochemical side‑reactions with molecular oxygen during device operation. We show that this electrochemical side reaction yields hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), a reactive side‑product, which may be harmful to the local biological environment and may also accelerate device degradation. We report a design strategy for the development of redox-active organic semiconductors based on donor-acceptor copolymers that prevent the formation of H<sub>2</sub>O<sub>2</sub> during device operation. This study elucidates the previously overlooked side-reactions between redox-active conjugated polymers and molecular oxygen in electrochemical devices for bioelectronics, which is critical for the operation of electrolyte‑gated devices in application-relevant environments.</p>


2020 ◽  
Vol 5 (10) ◽  
pp. 1407-1414
Author(s):  
Abheek Datta ◽  
Zakaria Ziadi ◽  
Pawan Kumar ◽  
Toshio Sasaki ◽  
Eric Danielson ◽  
...  

A new interaction triumvirate of N–Pt–Ti is established via ballistic bombardment of Pt nanoparticles on TiN films.


1964 ◽  
Vol 17 (11) ◽  
pp. 1229 ◽  
Author(s):  
T Mole ◽  
JR Surtees

The reactions of trimethyl-, triethyl-, tripropyl-, tri-isobutyl-, and triphenylaluminium with phenylacetylene in the presence and absence of benzene or toluene have been studied. In every case phenylethynylaluminium compounds are formed. Dimethyl(phenylethynyl)aluminium and diphenyl(phenylethynyl)aluminium are crystalline solids. The former compound disproportionates partially in ethereal solution. Side reactions competing with the formation of phenylethynylaluminium compounds are also observed. Triethylaluminium and tripropylaluminium add to phenylacetylene to give PhC(AlR2)=CHR (R = Et, Pr), but these alkenylaluminium compounds metallate further phenylacetylene and are so transformed to alkenes. A similar process occurs in the reaction with triphenylaluminium, but in this case both possible products of cis addition are observed. Tri-isobutylaluminium yields phenylethenyl compounds by reduction of the triple bond in the principal side reaction.


2012 ◽  
Vol 15 (3) ◽  
pp. E14 ◽  
Author(s):  
Rima J. Isaifan ◽  
Holly A. E. Dole ◽  
Emil Obeid ◽  
Leonardo Lizarraga ◽  
Philippe Vernoux ◽  
...  

2021 ◽  
Author(s):  
Hee Jeong Im ◽  
Yong Joon Park

Abstract Lithia (Li2O)-based cathodes, utilizing oxygen redox reactions for obtaining capacity, exhibit higher capacity than commercial cathodes. However, they are highly reactive owing to superoxides formed during charging, and they enable more active parasitic (side) reactions at the cathode/electrolyte and cathode/binder interfaces than conventional cathodes. This causes deterioration of the electrochemical performance limiting commercialization. To address these issues, the binder and salt for electrolyte were replaced in this study to reduce the side reaction of the cells containing lithia-based cathodes. The commercially used polyvinylidene fluoride (PVDF) binder and LiPF6 salt in the electrolyte easily generate such reactions, and the subsequent reaction between PVDF and LiOH (from decomposition of lithia) causes slurry gelation and agglomeration of particles in the electrode. Moreover, the fluoride ions from PVDF promote side reactions, and LiPF6 salt forms POF3 and HF, which cause side reactions owing to hydrolysis in organic solvents containing water. However, the polyacrylonitrile (PAN) binder and LiTFSI salt decrease these side reactions owing to their high stability with lithia-based cathode. Further, thickness of the interfacial layer was reduced, resulting in decreased impedance value of cells containing lithia-based cathodes. Consequently, for the same lithia-based cathodes, available capacity and cyclic performance were increased owing to the effects of PAN binder and LiTFSI salt in the electrolyte.


Synthesis ◽  
2020 ◽  
Vol 52 (21) ◽  
pp. 3189-3210
Author(s):  
Ayman El-Faham ◽  
Fernando Albericio ◽  
Srinivasa Rao Manne ◽  
Beatriz G. de la Torre

AbstractOxymaPure [ethyl 2-cyano-2-(hydroxyimino)acetate] is an exceptional reagent with which to suppress racemization and enhance coupling efficiency during amide bond formation. The tremendous popularity of OxymaPure has led to the development of several Oxyma-based reagents. OxymaPure and its derived reagents are widely used in solid- and solution-phase peptide chemistry. This review summarizes the recent developments and applications of OxymaPure and Oxyma-based reagents in peptide chemistry, in particular in solution-phase chemistry. Moreover, the side reaction associated with OxymaPure is also discussed.1 Introduction2 Oxyma-Based Coupling Reagents2.1 Aminium/Uronium Salts of OxymaPure2.2 Phosphonium Salts of OxymaPure2.3 Oxyma-Based Phosphates2.4 Sulfonate Esters of OxymaPure2.5 Benzoate Esters of OxymaPure2.6 Carbonates of OxymaPure Derivatives3 OxymaPure Derivatives4 Other Oxime-Based Additives and Coupling Reagents5 Side Reactions Using OxymaPure Derivatives6 Conclusion7 List of Abbreviations


2019 ◽  
Author(s):  
Alexander Giovannitti ◽  
Reem B. Rashid ◽  
Quentin Thiburce ◽  
Bryan D. Paulsen ◽  
Camila Cendra ◽  
...  

<p>Avoiding faradaic side reactions during the operation of electrochemical devices is important to enhance the device stability, to achieve low power consumption, and to prevent the formation of reactive side‑products. This is particularly important for bioelectronic devices which are designed to operate in biological systems. While redox‑active materials based on conducting and semiconducting polymers represent an exciting class of materials for bioelectronic devices, they are susceptible to electrochemical side‑reactions with molecular oxygen during device operation. We show that this electrochemical side reaction yields hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), a reactive side‑product, which may be harmful to the local biological environment and may also accelerate device degradation. We report a design strategy for the development of redox-active organic semiconductors based on donor-acceptor copolymers that prevent the formation of H<sub>2</sub>O<sub>2</sub> during device operation. This study elucidates the previously overlooked side-reactions between redox-active conjugated polymers and molecular oxygen in electrochemical devices for bioelectronics, which is critical for the operation of electrolyte‑gated devices in application-relevant environments.</p>


2008 ◽  
Vol 112 (27) ◽  
pp. 10209-10213 ◽  
Author(s):  
Z.-H. Qin ◽  
M. Lewandowski ◽  
Y.-N. Sun ◽  
S. Shaikhutdinov ◽  
H.-J. Freund

2020 ◽  
Vol 92 (3) ◽  
pp. 413-427 ◽  
Author(s):  
Robinson B. Dinamarca ◽  
Rodrigo Espinoza-González ◽  
Cristian H. Campos ◽  
Gina Pecchi

AbstractThis study reports the catalytic preparation, characterization, and evaluation of nanoscale core-shell structures with a γ-Fe2O3 core covered by a SiO2 monoshell or by a SiO2@TiO2 multishell as a support for Pt nanoparticles (NPs) to synthesize active and operationally stable catalysts for selective liquid-phase cinnamaldehyde hydrogenation. The structures were designed with a magnetic core so they could be easily recovered from the catalytic bed by simple magnetization and with a SiO2 monoshell or a SiO2@TiO2 multishell to protect the magnetic core. At the same time, this study details the effect of the shell on the catalytic performance. Moreover, the effect of particle size on the selective production of cinnamyl alcohol was studied by preparing two families of catalysts with metal loadings of 1 wt% and 5 wt% Pt with respect to the core-shell. The particle size effect enabled the Fe2O3@SiO2-5%Pt system, with an average particle size of 5.6 nm, to reach 100 % conversion of cinnamaldehyde at 300 min of reaction, producing cinnamyl alcohol with 90 % selectivity; this result differed greatly from that of the Fe2O3@SiO2-1%Pt (dPt = 3.5 nm) system, which reached a maximum conversion at 600 min with 49 % selectivity for the product of interest. However, the Fe2O3@SiO2@TiO2-x%Pt systems showed lower levels of conversion and selectivity compared to those of the Fe2O3@SiO2-x%Pt catalysts, which is attributed to the fact that average metal particle sizes below 5.0 nm were obtained in both cases. After reduction in H2 at 773 K, the Fe2O3@SiO2@TiO2-1%Pt catalyst showed deactivation, reaching 10 % conversion at 600 min of reaction and 60 % selectivity for the product of interest. However, the reduced Fe2O3@SiO2@TiO2-5%Pt system showed 98 % conversion with 95 % selectivity for cinnamyl alcohol at 24 h of operation; the increase in selectivity is attributed to the combined effects of the increase in average particle size (~7.5 nm) and the presence of strong metal-support interaction – SMSI – effects after reduction. Finally, the most selective systems were tested for operational stability, where the Fe2O3@SiO2@-5%Pt catalyst could be reused in three consecutive operating cycles while maintaining its activity and selectivity for cinnamyl alcohol – unlike the Fe2O3@SiO2@TiO2-5%Pt reduced system, which was deactivated after the third reaction cycle due to active phase leaching.


2000 ◽  
Vol 18 (1) ◽  
pp. 65-74
Author(s):  
L.A. Belyakova ◽  
A.M. Varvarin

The solid-phase thermal and catalytic hydrosilylation of N-vinyl-2-pyrrolidone on the surface of hydride silicas has been studied. It was established that thermal polymerization of N-vinyl-2-pyrrolidone occurs as a side reaction during the thermal hydrosilylation of N-vinyl-2-pyrrolidone. It has also been found that the interaction of silicon hydride groups with water and propan-2-ol, as well as the formation of metallic platinum occur as side reactions during the catalytic hydrosilylation of N-vinyl-2-pyrrolidone on the surface of hydride silicas. Thermal hydrosilylation of N-vinyl-2-pyrrolidone in the absence of a catalyst and solvent is much preferred for the chemical bonding of N-vinyl-2-pyrrolidone in the surface layer of hydride silicas.


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