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Polypropylene Samples (polypropylene + sample)

Distribution by Scientific Domains
Polymers and Materials Science100%

Selected Abstracts

Study on Flow Induced Nano Structures in iPP with Different Molecular Weight and Resulting Strength Behavior

MACROMOLECULAR SYMPOSIA, Issue 1 2010
Achim Frick
Abstract Polypropylene samples in a wide molecular weight range between approx. 100,kg/mol to 1 600,kg/mol were processed by injection molding to thin walled micro specimens with respect to study shear induced crystallization phenomena under high shear rate and subsequently possible self reinforcement effects. The specimens nano structures were investigated and related deformation behavior under tensile studied. Novel morphologies have been detect and their micromechanical mechanism interpret and summarized. [source]

Crystal form and orientation of isotactic polypropylene samples prepared by vibration-injection molding

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007
Jie Zhang
Abstract A vibration,injection molding equipment was developed to prepare isotactic polypropylene injection samples to investigate their crystal form and orientation. Wide-angle X-ray scattering experiments (WAXD) were conducted in two modes: theta,theta mode and tube-fixed mode. Through vibration,injection molding, in additional to , form, , form, or , form can be obtained under different conditions. At high melt temperature (230), ,-PP can be induced and the core of the sample contains more ,-PP than the surface. At low melt temperature (190), ,-PP can be induced and the core and the surface of the sample contain approximate same proportion of ,-PP. Pole figures show that ,-PP of a static sample just orientates slightly along M direction, while that of vibration samples orientate much stronger. The orientation of the normal of (040), plane of the sample obtained at T = 230°C, f = 0.5 Hz, and Pv = 75MPa is preferred in M direction, and the orientation of the normal of (040), plane of the sample obtained at T = 190°C, f = 1.5 Hz, and Pv= 35 MPa is preferred in N direction. ,-PP and ,-PP do not show obvious orientation. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source]

Synthesis of branched polypropylene with isotactic backbone and atactic side chains by binary iron and zirconium single-site catalysts

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 8 2003
Zhibin Ye
Abstract This article reports the use of a binary single-site catalyst system for synthesizing comb-branched polypropylene samples having isotactic polypropylene (iPP) backbones and atactic polypropylene (aPP) side chains from propylene feedstock. This catalyst system consisted of the bisiminepyridine iron catalyst {[2-ArNC(Me)]2C5H3N}FeCl2 [Ar = 2,6-C6H3(Me)2] (1) and the zirconocene catalyst rac -Me2Si(2-MeBenz[e]Ind)2ZrCl2 (2). The former in situ generated 1-propenyl-ended aPP macromonomer, whereas the latter incorporated the macromonomer into the copolymer. The effects of reaction conditions, such as the catalyst addition procedure and the ratio of 1/2 on the branching frequency, were examined. Copolymer samples having a branching density up to 8.6 aPP side chains per 1000 iPP monomer units were obtained. The branched copolymers were characterized by 13C NMR and differential scanning calorimetry. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1152,1159, 2003 [source]

Comparison of structure development in injection molding of isotactic and syndiotactic polypropylenes

POLYMER ENGINEERING & SCIENCE, Issue 8 2002
Dongman Choi
A comparative study of the crystallization and orientation development in injection molding isotactic and syndiotactic polypropylenes was made. The injection molded samples were characterized using wide angle X-ray diffraction (WAXD) techniques and birefringence. The injection molded isotactic polypropylene samples formed well-defined sublayers (skin, shear and core zones) and exhibited polymorphic crystal structures of the monoclinic ,-form and the hexagonal ,-form. Considerable amounts of ,-form crystal were formed in the shear and core zones, depending on the injection pressure or on the packing pressure. The isotactic polypropylene samples had relatively high frozen-in orientations in the skin layer and the shear zone. The injection molded syndiotactic polypropylene exhibited the disordered Form I structure, but it did not appear to crystallize during the mold-filling stage because of its slow crystallization rate and to develop a distinct shear zone. The core zone orientation was greatly increased by application of high packing pressure. The isotactic polypropylene samples exhibited much higher birefringence than the syndiotactic polypropylene samples at the skin and shear layers, whereas both materials exhibited similar levels of crystalline orientation in these layers. [source]