Ex situ synthesis and characterization of a polymer-carbon nanotube-based hybrid nanocatalyst with one of the highest catalytic activities and stabilities for the hydrolytic dehydrogenation of hydrazine-borane at room temperature conditions

2019 ◽  
Vol 552 ◽  
pp. 432-438 ◽  
Author(s):  
Buse Demirkan ◽  
Esra Kuyuldar ◽  
Yaşar Karataş ◽  
Mehmet Gülcan ◽  
Fatih Sen
Polymer ◽  
2017 ◽  
Vol 118 ◽  
pp. 68-74 ◽  
Author(s):  
Muhammad Nisar ◽  
Carlos Pérez Bergmann ◽  
Julian Geshev ◽  
Raúl Quijada ◽  
Griselda Barrera Galland

RSC Advances ◽  
2021 ◽  
Vol 11 (22) ◽  
pp. 13245-13255
Author(s):  
Mehdi Davoodi ◽  
Fatemeh Davar ◽  
Mohammad R. Rezayat ◽  
Mohammad T. Jafari ◽  
Mehdi Bazarganipour ◽  
...  

New nanocomposite of zeolitic imidazolate framework-67@magnesium aluminate spinel (ZIF-67@MgAl2O4) has been fabricated by a simple method at room temperature with different weight ratios.


2009 ◽  
Vol 1240 ◽  
Author(s):  
Ji-Ye Kang ◽  
Su-Mi Eo ◽  
Loon-Seng Tan ◽  
Jong-Beom Baek

AbstractSingle-walled carbon nanotube (SWCNT) and multi-walled carbon nanotube (MWCNT) were functionalized with 3,4-diaminobenzoic acid via “direct” Friedel-Crafts acylation reaction in PPA/P2O5 to afford ortho-diamino-functionalized SWCNT (DIF-SWCNT) and MWCNT (DIF-MWCNT). The resultant DIF-SWCNT and DIF-MWCNT showed improved solubility and dispersibility. To improve interfacial adhesion between CNT and polymer matrix, the grafting of ABPBI onto the surface of DIF-SWCNT (10 wt%) or DIF-MWCNT (10 wt%) was conducted by simple in-situ polymerization of AB monomer, 3,4-diaminobenzoic acid dihydrochloride, in PPA. The resultant ABPBI-g-MWCNT and ABPBI-g-SWCNT showed improved the mechanical and electrical properties.


2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Evelyn Carolina Martínez Ceballos ◽  
Ricardo Vera Graziano ◽  
Gonzalo Martínez Barrera ◽  
Oscar Olea Mejía

Poly(dichlorophosphazene) was prepared by melt ring-opening polymerization of the hexachlorocyclotriphosphazene. Poly[bis(2-hydroxyethyl-methacrylate)-phosphazene] and poly[(2-hydroxyethyl-methacrylate)-graft-poly(lactic-acid)-phosphazene] were obtained by nucleophilic condensation reactions at different concentrations of the substituents. The properties of the synthesized copolymers were assessed by FTIR,1H-NMR and31P-NMR, thermal analysis (DSC-TGA), and electron microscopy (SEM). The copolymers have a block structure and show twoTg's below room temperature. They are stable up to a temperature of 100°C. The type of the substituents attached to the PZ backbone determines the morphology of the polymers.


Carbon ◽  
2006 ◽  
Vol 44 (5) ◽  
pp. 848-853 ◽  
Author(s):  
Vassilios Tzitzios ◽  
Vasilios Georgakilas ◽  
Eudokia Oikonomou ◽  
Michael Karakassides ◽  
Dimitrios Petridis

2008 ◽  
Vol 29 (4) ◽  
pp. 451-457 ◽  
Author(s):  
Te-Cheng Mo ◽  
Hong-Wen Wang ◽  
San-Yan Chen ◽  
Yun-Chieh Yeh

2020 ◽  
Author(s):  
Joel D. Smith ◽  
George Durrant ◽  
Daniel Ess ◽  
Warren Piers

<div>The synthesis and characterization of an iridium polyhydride complex (Ir-H4)</div><div>supported by an electron-rich PCP framework is described. This complex readily loses molecular</div><div>hydrogen allowing for rapid room temperature hydrogen isotope exchange (HIE) at the hydridic</div><div>positions and the α-C-H site of the ligand with deuterated solvents such as benzene-d6, toluene-d8</div><div>and THF-d8. The removal of 1-2 equivalents of molecular H2 forms unsaturated iridium carbene</div><div>trihydride (Ir-H3) or monohydride (Ir-H) compounds that are able to create further unsaturation</div><div>by reversibly transferring a hydride to the ligand carbene carbon. These species are highly active</div><div>hydrogen isotope exchange (HIE) catalysts using C6D6 or D2O as deuterium sources for the</div><div>deuteration of a variety of substrates. By modifying conditions to influence the Ir-Hn speciation,</div><div>deuteration levels can range from near exhaustive to selective only for sterically accessible sites.</div><div>Preparative level deuterations of select substrates were performed allowing for procurement of</div><div>>95% deuterated compounds in excellent isolated yields; the catalyst can be regenerated by</div><div>treatment of residues with H2 and is still active for further reactions.</div>


Author(s):  
U. Mahaboob Basha ◽  
D. Mohana Krishnudu ◽  
P. Hussain ◽  
K. Manohar Reddy ◽  
N. Karthikeyan ◽  
...  

In the current work epoxy resin is chosen as matrix, treated Sacharum offinarum ( SugarCane) fiber, Pennisetum typhoides (Jowar)/ Fillet miller (Ragi) filler are chosen as reinforcement. Room temperature cured Epoxy System filled with Sacharum offinarum fiber and Pennisetum typhoides (Jowar)/ Fillet miller (Ragi) filler are synthesised by mechanical shear mixer, then kept in a Ultra sonic Sonicator for better dispersion of Pennisetum typhoides (Jowar)/ Fillet miller (Ragi) filler in the matrix. Different weights of modified Pennisetum typhoides (Jowar)/ Fillet miller (Ragi) filler (1,2,3,4,5 gm wt) has been incorporated into the Epoxy matrix in order to study the variation of Mechanical and Thermal properties.


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