Influence of the ultrasonic-assisted synthesis on Al distribution in MOR zeolite. From gel to resulting material

2021 ◽  
Author(s):  
Joanna Elzbieta Olszowka ◽  
Veronika Pashkova ◽  
Agnieszka Kornas ◽  
Jiri Dedecek ◽  
Jiri Brus ◽  
...  
Keyword(s):  
Ultrasonic Pretreatment ◽  
Ultrasonic Assisted ◽  
Synthesis Procedure ◽  
Al Distribution

Two Al-rich mordenite samples were prepared by the same synthesis procedure except for the activation of the gel for which classical stirring and ultrasonic pretreatment was used. The organization of...

Epitaxy and texture analysis of Bi-Sr-Ca-Cu-O thin films on (100) MgO using Transmission Electron Microscopy

1990 ◽  
Vol 48 (4) ◽  
pp. 68-69
Author(s):  
J. T. Sizemore ◽  
D. G. Schlom ◽  
Z. J. Chen ◽  
J. N. Eckstein ◽  
I. Bozovic ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Transmission Electron Microscopy ◽  
Critical Currents ◽  
Unit Cell ◽  
X Ray Diffraction ◽  
Cell Axis ◽  
Transmission Electron ◽  
Synthesis Procedure

Investigators observe large critical currents for superconducting thin films deposited epitaxially on single crystal substrates. The orientation of these films is often characterized by specifying the unit cell axis that is perpendicular to the substrate. This omits specifying the orientation of the other unit cell axes and grain boundary angles between grains of the thin film. Misorientation between grains of YBa2Cu3O7−δ decreases the critical current, even in those films that are c axis oriented. We presume that these results are similar for bismuth based superconductors and report the epitaxial orientations and textures observed in such films.Thin films of nominally Bi2Sr2CaCu2Ox were deposited on MgO using molecular beam epitaxy (MBE). These films were in situ grown (during growth oxygen was incorporated and the films were not oxygen post-annealed) and shuttering was used to encourage c axis growth. Other papers report the details of the synthesis procedure. The films were characterized using x-ray diffraction (XRD) and transmission electron microscopy (TEM).

A Mild and Simple Method for Making MIDA Boronates

2020 ◽  
Author(s):  
Aidan Kelly ◽  
Peng-Jui (Ruby) Chen ◽  
Jenna Klubnick ◽  
Daniel J. Blair ◽  
Martin D. Burke
Keyword(s):  
Organic Synthesis ◽  
Boronic Acids ◽  
Simple Method ◽  
Direct Preparation ◽  
Synthesis Procedure ◽  
Harsh Conditions

<div> <div> <div> <p>Existing methods for making MIDA boronates require harsh conditions and complex procedures to achieve dehydration. Here we disclose that a pre-dried form of MIDA, MIDA anhydride, acts as both a source of the MIDA ligand and an in situ desiccant to enable a mild and simple MIDA boronate synthesis procedure. This method expands the range of sensitive boronic acids that can be converted into their MIDA boronate counterparts. Further utilizing unique properties of MIDA boronates, we have developed a MIDA Boronate Maker Kit which enables the direct preparation and purification of MIDA boronates from boronic acids using only heating and centrifuge equipment that is widely available in labs that do not specialize in organic synthesis. </p> </div> </div> </div>

Enzymatic Iodination of Maleic and Fumaric Acids Diethyl Esters

2009 ◽  
Vol 59 (12) ◽  
pp. 1400-1404
Author(s):  
Marius Tudorascu ◽  
Spiridon Oprea ◽  
Afrodita Doina Marculescu ◽  
Stefania Tudorascu
Keyword(s):  
Hydrogen Peroxide ◽  
Tartaric Acid ◽  
Disperse System ◽  
Hydrogen Peroxide Solution ◽  
Ultrasonic Pretreatment ◽  
Tartaric Acids ◽  
Inactive Form ◽  
Generating System ◽  
Sole Product

The mechanism of the enzymatic iodination process of diethylmaleate and diethylfumarate (which present no miscibility with water) in the presence of lactoperoxidase, both in diluted hydrogen peroxide solution and in a generating system of hydrogen peroxide using ammonium and calcium iodides as halide sources in disperse system (after an ultrasonic pretreatment) was studied. The obtained sole product (diethyl-2, 3-diiodosuccinate) after the enzymatic iodination process was directly hydrolyzed to a tartaric acid present in an optically inactive form. The mechanism of obtaining the intermediate and final products and respectively, the existence of both D, L-tartaric acid and meso-tartaric acids (as lithium bitartrates) were also investigated.

Positive Role of Synthesis Method and Hard Template on the Catalytic Performance of SAPO-34 in Methanol to Olefin Reaction.

2020 ◽  
Vol 23 ◽  
Author(s):  
Sajjad Rimaz ◽  
Reza Katal
Keyword(s):  
Particle Size ◽  
Synthesis Method ◽  
Catalytic Performance ◽  
Hard Template ◽  
Structure Directing Agent ◽  
Positive Role ◽  
Methanol To Olefin ◽  
Dg Method ◽  
Synthesis Procedure

: In the present study, SAPO-34 particles were synthesized using hydrothermal (HT) and dry gel (DG) conversion methods in the presence of diethyl amine (DEA) as an organic structure directing agent (SDA). Carbon nanotubes (CNT) were used as hard template in the synthesis procedure to introduce transport pores into the structures of the synthesized samples. The synthesized samples were characterized with different methods to reveal effects of synthesis method and using hard template on their structure and catalytic performance in methanol to olefin reaction (MTO). DG conversion method results in smaller particle size in comparison with hydrothermal method, resulting in enhancing catalytic performance. On the other side, using CNT in the synthesis procedure with DG method results in more reduction in particle size and formation of hierarchical structure which drastically improves catalytic performance.

Ultrasonic-Assisted Surface- Modification of Nanosilica Chloride and its Use for Synthesis of 3,4- Dihydropyrimidinones

2014 ◽  
Vol 11 (5) ◽  
pp. 361-367 ◽  
Author(s):  
Mahgol Tajbakhsh ◽  
Yousef Ranjbar ◽  
Abdolhosein Masuodi ◽  
Parizad Rezaee ◽  
Mahmood Tajbakhsh ◽  
...  
Keyword(s):  
Surface Modification ◽  
Ultrasonic Assisted
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