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Hybrid Catalysts (hybrid + catalyst)

Distribution by Scientific Domains
Polymers and Materials Science66%
Chemistry33%

Selected Abstracts

Ziegler-Natta/Metallocene Hybrid Catalyst for Ethylene Polymerization

MACROMOLECULAR REACTION ENGINEERING, Issue 6 2007
Mostafa Ahmadi
Abstract A Ziegler-Natta/metallocene hybrid catalyst was produced and utilized in the polymerization of ethylene with the aim of producing bimodal polyethylene. The MgCl2 adduct was prepared by a melt quenching method and Cp2ZrCl2 and TiCl4 catalysts were loaded, respectively, after treating the surface with TiBAl. The polymerization kinetics involved an induction period, followed by fragmentation and expansion of particles. SEM micrographs revealed that the spherical morphology was retained through the initial mild reaction conditions of induction period. The polymers produced showed bimodal molecular weight distribution patterns, suggesting that both components of the hybrid catalyst were active over the support. [source]

ChemInform Abstract: Highly Active and Robust Organic,Inorganic Hybrid Catalyst for the Synthesis of Cyclic Carbonates from Carbon Dioxide and Epoxides.

CHEMINFORM, Issue 31 2008
Takashi Sakai
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

Hybrid titanium catalyst supported on core-shell silica/poly(styrene- co -acrylic acid) carrier

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2010
Lijun Du
Abstract Hybrid titanium catalysts supported on silica/poly(styrene- co -acrylic acid) (SiO2/PSA) core-shell carrier were prepared and studied. The resulting catalysts were characterized by Fourier transform infrared (FTIR) spectroscopy, laser scattering particle analyzer and scanning electronic microscope (SEM). The hybrid catalyst (TiCl3/MgCl2/THF/SiO2·TiCl4/MgCl2/PSA) showed core-shell structure and the thickness of the PSA layer in the two different hybrid catalysts was 2.0 ,m and 5.0 ,m, respectively. The activities of the hybrid catalysts were comparable to the conventional titanium-based Ziegler-Natta catalyst (TiCl3/MgCl2/THF/SiO2). The hybrid catalysts showed lower initial polymerization rate and longer polymerization life time compared with TiCl3/MgCl2/THF/SiO2. The activities of the hybrid catalysts were enhanced firstly and then decreased with increasing P/P. Higher molecular weight and broader molecular weight distribution (MWD) of polyethylene produced by the core-shell hybrid catalysts were obtained. Particularly, the hybrid catalyst with a PSA layer of 5.0 ,m obtained the longest polymerization life time with the highest activity (2071 kg PE mol,1 Ti h,1) and the resulting polyethylene had the broadest MWD (polydispersity index = 11.5) under our experimental conditions. The morphology of the polyethylene particles produced by the hybrid catalysts was spherical, but with irregular subparticles due to the influence of PSA layer. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]

Ziegler-Natta/Metallocene Hybrid Catalyst for Ethylene Polymerization

MACROMOLECULAR REACTION ENGINEERING, Issue 6 2007
Mostafa Ahmadi
Abstract A Ziegler-Natta/metallocene hybrid catalyst was produced and utilized in the polymerization of ethylene with the aim of producing bimodal polyethylene. The MgCl2 adduct was prepared by a melt quenching method and Cp2ZrCl2 and TiCl4 catalysts were loaded, respectively, after treating the surface with TiBAl. The polymerization kinetics involved an induction period, followed by fragmentation and expansion of particles. SEM micrographs revealed that the spherical morphology was retained through the initial mild reaction conditions of induction period. The polymers produced showed bimodal molecular weight distribution patterns, suggesting that both components of the hybrid catalyst were active over the support. [source]

Hybrid titanium catalyst supported on core-shell silica/poly(styrene- co -acrylic acid) carrier

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2010
Lijun Du
Abstract Hybrid titanium catalysts supported on silica/poly(styrene- co -acrylic acid) (SiO2/PSA) core-shell carrier were prepared and studied. The resulting catalysts were characterized by Fourier transform infrared (FTIR) spectroscopy, laser scattering particle analyzer and scanning electronic microscope (SEM). The hybrid catalyst (TiCl3/MgCl2/THF/SiO2·TiCl4/MgCl2/PSA) showed core-shell structure and the thickness of the PSA layer in the two different hybrid catalysts was 2.0 ,m and 5.0 ,m, respectively. The activities of the hybrid catalysts were comparable to the conventional titanium-based Ziegler-Natta catalyst (TiCl3/MgCl2/THF/SiO2). The hybrid catalysts showed lower initial polymerization rate and longer polymerization life time compared with TiCl3/MgCl2/THF/SiO2. The activities of the hybrid catalysts were enhanced firstly and then decreased with increasing P/P. Higher molecular weight and broader molecular weight distribution (MWD) of polyethylene produced by the core-shell hybrid catalysts were obtained. Particularly, the hybrid catalyst with a PSA layer of 5.0 ,m obtained the longest polymerization life time with the highest activity (2071 kg PE mol,1 Ti h,1) and the resulting polyethylene had the broadest MWD (polydispersity index = 11.5) under our experimental conditions. The morphology of the polyethylene particles produced by the hybrid catalysts was spherical, but with irregular subparticles due to the influence of PSA layer. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]

A Robust Protein Host for Anchoring Chelating Ligands and Organocatalysts

CHEMBIOCHEM, Issue 4 2008
Manfred T. Reetz Prof. Dr.
Abstract In order to put the previously proposed concept of directed evolution of hybrid catalysts (proteins that harbor synthetic transition-metal catalysts or organocatalysts) into practice, several prerequisites must be met. The availability of a robust host protein that can be expressed in sufficiently large amounts, and that can be purified in a simple manner is crucial. The thermostable enzyme tHisF from Thermotoga maritima, which constitutes the synthase subunit of a bi-enzyme complex that is instrumental in the biosynthesis of histidine, fulfills these requirements. In the present study, fermentation has been miniaturized and parallelized, as has purification of the protein by simple heat treatment. Several mutants with strategically placed cysteines for subsequent bioconjugation have been produced. One of the tHisF mutants, Cys9Ala/Asp11Cys, was subjected to bioconjugation by the introduction of a variety of ligands for potential metal ligation, of a ligand/metal moiety, and of several organocatalytic entities that comprise a flavin or thiazolium salts. Characterization by mass spectrometry and tryptic digestion was achieved. As a result of this study, a platform for performing future directed evolution of these hybrid catalysts is now available. [source]

An Efficient Hybrid, Nanostructured, Epoxidation Catalyst: Titanium Silsesquioxane,Polystyrene Copolymer Supported on SBA-15

CHEMISTRY - A EUROPEAN JOURNAL, Issue 4 2007
Lei Zhang
Abstract A novel interfacial hybrid epoxidation catalyst was designed with a new immobilization method for homogeneous catalysts by coating an inorganic support with an organic polymer film containing active sites. The titanium silsesquioxane (TiPOSS) complex, which contains a single-site titanium active center, was immobilized successfully by in-situ copolymerization on a mesoporous SBA-15-supported polystyrene polymer. The resulting hybrid materials exhibit attractive textural properties (highly ordered mesostructure, large specific surface area (>380,m2,g,1) and pore volume (,0.46,cm3,g,1)), and high activity in the epoxidation of alkenes. In the epoxidation of cyclooctene with tert -butyl hydrogen peroxide (TBHP), the hybrid catalysts have rate constants comparable with that of their homogeneous counterpart, and can be recycled at least seven times. They can also catalyze the epoxidation of cyclooctene with aqueous H2O2 as the oxidant. In two-phase reaction media, the catalysts show much higher activity than their homogeneous counterpart due to the hydrophobic environment around the active centers. They behave as interfacial catalysts due to their multifunctionality, that is, the hydrophobicity of polystyrene and the polyhedral oligomeric silsesquioxanes (POSS), and the hydrophilicity of the silica and the mesoporous structure. Combination of the immobilization of homogeneous catalysts on two conventional supports, inorganic solid and organic polymer, is demonstrated to achieve novel heterogeneous catalytic ensembles with the merits of attractive textural properties, tunable surface properties, and optimized environments around the active sites. [source]