Books > Professional & Technical > Industrial chemistry & manufacturing technologies > Industrial chemistry
|
Buy Now
MWW-Type Titanosilicate - Synthesis, Structural Modification and Catalytic Applications to Green Oxidations (Paperback, 2013 ed.)
Loot Price: R1,853
Discovery Miles 18 530
|
|
MWW-Type Titanosilicate - Synthesis, Structural Modification and Catalytic Applications to Green Oxidations (Paperback, 2013 ed.)
Series: SpringerBriefs in Green Chemistry for Sustainability
Expected to ship within 10 - 15 working days
|
This book provides a comprehensive review of a new generation of
selective oxidation titanosilicate catalysts with the MWW topology
(Ti-MWW) based on the research achievements of the past 12 years.
It gives an overview of the synthesis, structure modification and
catalytic properties of Ti-MWW. Ti-MWW can readily be prepared by
means of direct hydrothermal synthesis with
crystallization-supporting agents, using dual-structure-directing
agents and a dry-gel conversion technique. It also can be
post-synthesized through unique reversible structure transformation
and liquid-phase isomorphous substitution. The structural
conversion of Ti-MWW into the materials usable for processing large
molecules is summarized. Taking advantage of the structure
diversity of the lamellar precursor of Ti-MWW, it can be fully or
partially delaminated, and undergo interlayer silylation to obtain
a novel structure with larger porosity. In the selective oxidation
(alkene epoxidation and ketone/aldehyde ammoximation) with hydrogen
peroxide or organic peroxide as an oxidant, the unique catalytic
properties of Ti-MWW are described in comparison to conventional
titanosilicates such as TS-1 and Ti-Beta.
General
Is the information for this product incomplete, wrong or inappropriate?
Let us know about it.
Does this product have an incorrect or missing image?
Send us a new image.
Is this product missing categories?
Add more categories.
Review This Product
No reviews yet - be the first to create one!
|
|
Email address subscribed successfully.
A activation email has been sent to you.
Please click the link in that email to activate your subscription.