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Zirconium Dichloride (zirconium + dichloride)

Distribution by Scientific Domains

Polymers and Materials Science	100%

Selected Abstracts

Catalytic synthesis of styryl-capped isotactic polypropylenes

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2010
Huahua Huang
Abstract Bis-styrenic molecules, 1,4-divinylbenzene (DVB) and 1,2-bis(4-vinylphenyl)ethane (BVPE), were successfully combined with hydrogen (H2) to form consecutive chain transfer complexes in propylene polymerization mediated by an isospecific metallocene catalyst (i.e., rac -dimethylsilylbis(2-methyl-4-phenylindenyl)zirconium dichloride, I) activated with methylaluminoxane (MAO), rendering a catalytic access to styryl-capped isotactic polypropylenes (i -PP). The chain transfer reaction took place in a unique way where prior to the ultimate chain transfer DVB/H2 or BVPE/H2 caused a copolymerization-like reaction leading to the formation of main chain benzene rings. A preemptive polymer chain reinsertion was deduced after the consecutive actions of DVB/H2 or BVPE/H2, which gave the styryl-terminated polymer chain alongside a metal-hydride active species. It was confirmed that the chain reinsertion occurred in a regio-irregular 1,2-fashion, which contrasted with a normal 2,1-insertion of styrene monomer and ensured subsequent continuous propylene insertions, directing the polymerization to repeated DVB or BVPE incorporations inside polymer chain. Only as a competitive reaction, the insertion of propylene into metal-hydride site broke the chain propagation resumption process while completed the chain transfer process by releasing the styryl-terminated polymer chain. BVPE was found with much higher chain transfer efficiency than DVB, which was attributed to its non-conjugated structure with much divided styrene moieties resulting in higher polymerization reactivity but lower chain reinsertion tendency. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3709,3713, 2010 [source]

Copolymerization of ethylene and N -(vinylphenyl)carbazole with titanium and zirconium catalysts

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 4 2005
Naofumi Naga
Copolymerization of ethylene and N -(vinylphenyl)carbazole (VPC) was investigated with dimethylsilylene(tetramethylcyclopentadienyl)(N-tert -butyl)titanium dichloride (1) and isopropylidenebis(indenyl)zirconium dichloride (2) catalysts. The corresponding copolymers were obtained in the copolymerization, and the copolymerization behavior and structure of the resulting copolymer were studied. [source]

Copolymerization of ethylene with 1-hexene over metallocene catalyst supported on complex of magnesium chloride with tetrahydrofuran

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 10 2004
Krystyna Czaja
Abstract The study of ethylene/1-hexene copolymerization with the zirconocene catalyst, bis(cyclopentadienyl)zirconium dichloride (Cp2ZrCl2)/methylaluminoxane (MAO), anchored on a MgCl2(THF)2 support was carried out. The influence of 1-hexene concentration in the feed on catalyst productivity and comonomer reactivity as well as other properties was investigated. Additionally, the effect of support modification by the organoaluminum compounds [(MAO, trimethlaluminum (AlMe3), or diethylaluminum chloride (Et2AlCl)] on the behavior of the MgCl2(THF)2/Cp2ZrCl2/MAO catalyst in the copolymerization process and on the properties of the copolymers was explored. Immobilization of the Cp2ZrCl2 compound on the complex magnesium support MgCl2(THF)2 resulted in an effective system for the copolymerization of ethylene with 1-hexene. The modification of the support as well as the kind of organoaluminum compound used as a modifier influenced the activity of the examined catalyst system. Additionally, the profitable influence of immobilization of the homogeneous catalyst as well as modification of the support applied on the molecular weight and molecular weight distribution of the copolymers was established. Finally, with the successive self-nucleation/annealing procedure, the copolymers obtained over both homogeneous and heterogeneous metallocene catalysts were heterogeneous with respect to their chemical composition. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2512,2519, 2004 [source]

Gas-Phase Polymerization with Transition Metal Catalysts Supported on Montmorillonite , A Particle Morphological Study

MACROMOLECULAR SYMPOSIA, Issue 1 2009
Sang-Young A. Shin
Abstract This investigation focuses on the mechanism of particle fragmentation and growth when clay-supported metallocene catalysts are used to polymerize ethylene in gas-phase reactors. We supported bis(cyclopentadienyl)-zirconium dichloride (Cp2ZrCl2) on montmorillonite (MMT) pretreated with triisobutylaluminum and 10-undecence-1-ol to produce in-situ polyethylene-clay nanocomposites. During gas phase polymerization, the MMT layers were exfoliated by the growing polymer chains, starting from the openings of the clay galleries. After microtoming, the cross-section of the fragmented MMT particles showed bundles of distorted silicate layer stacks, proving that exfoliation took place during polymerization, producing an in-situ polyethylene-clay nanocomposite. Calculations of d-spacing by transmission electron microscopy (TEM) matched those measured by X-ray diffraction (XRD) analysis. [source]

Structure and properties of multi-walled carbon nanotubes/polyethylene nanocomposites synthesized by in situ polymerization with supported Cp2ZrCl2 catalyst

POLYMER COMPOSITES, Issue 3 2010
Shiyun Li
Multi-walled carbon nanotubes (MWCNTs)/polyethylene (PE) nanocomposites were prepared via in situ polymerization with MWCNTs supported Bis- (cyclopentadienyl) zirconium dichloride (Cp2ZrCl2) catalyst. X-ray photoelectron spectroscopy (XPS) and field emission scanning electron microscope (FESEM) results implied that Cp2ZrCl2 catalyst was immobilized in the surface of the MWCNTs supports via a bridge of methylaluminoxane (MAO). The efficient dispersion of MWCNTs in PE matrix and the strong compressive forces associated with PE on the MWCNTs were demonstrated by means of transmission electron microscope (TEM), FESEM and Raman spectra. With introducing 0.2 wt% MWCNTs, both the tensile strength and elongation of MWCNTs/PE nanocomposite were improved by factors of 1.6 (from 29 to 45 MPa) and 1.5 (from 909% to 1360%) comparing with the pure PE, respectively. Morphology observation of fractured surface revealed that the PE firmly adhered to the nanotubes, which was responsible for the significant improvement of the mechanical properties of nanocomposites. Thermal stabilities of the nanocomposites were significantly improved. In addition, the MWCNTs/PE nanocomposites showed very high ultraviolet (UV) shielding property, which could increase photooxidative stability of the PE. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers [source]