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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Advanced materials research Vol. 47-50 (June 2008), p. 765-768 
    ISSN: 1662-8985
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: A melt blending process was employed to prepare nano-composites based onthermoplastic polyurethane (TPU) and multi-walled carbon nanotubes (MWNT). The content ofMWNT filled in TPU was increased till 40phr (parts per hundreds of rubber). Scanning electronmicroscope (SEM) and transmission electron microscope (TEM) showed that the unmodifiedMWNT were dispersed uniformly in the TPU matrix beyond expectation. Dynamic mechanicalthermal analysis (DMTA) test demonstrated that the nano-composites possessed greatly increasedmodulus, and the flowing temperature moved to higher temperature with increasing MWNT content.Moreover, the nano-composites exhibited improved wear resistance, evidently increased thermalconductivity, and prominently raised electrical conductivity that might mean the TPU/MWNTnano-composites have potential application as multi-functional materials
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 1558-1562 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 39 (1993), S. 1455-1464 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A companion article (Chen and Hu, 1993a) discussed a statistical theory that for a system consisting of two closed subsystems, the residence time density (RTD) functions of the two subsystems will be statistically independent, if a two-dimensional perfect mixing exists at the subsystem boundary. In this case, the overall RTD function is related to that for individual subsystems through the convolution integral. This theory has been validated experimentally using two die-screw combinations.Based on this theory, a predictive RTD model for an intermeshing counterrotating twin-screw extruder has been developed. The screw in the longitudincl direction has been treated as C-chambers in series. The overall RTD of leakage flows has been calculated from the RTDs of these individual chambers and then converted into the RTD of the extruder. The predicted RTD has been tested against experimental results with success.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract This paper reports on the relative role of the functional group content and the molecular weight of a glycidyl methacrylate (GMA) functionalised PP (PP-g-GMA) as reactive compatibiliser in the compatibilisation of polypropylene (PP) and poly(butylene terephthalate) (PBT) immiscible blends in a co-rotating twin screw extruder. Two series of PP-g-GMA were compared in terms of their compatibilising effects on the morphology and mechanical properties (elongation at break and impact strength) of the blend. The first series of PP-g-GMA had the same molecular weight but different GMA contents while the second series of PP-g-GMA had the same GMA content but different molecular weights. The compatibilising effects of the first series of PP-g-GMA were dictated primarily by the amount of GMA in the blend, i.e., two PP-g-GMA having different GMA contents had the same compatibilising efficiency when the amount of GMA in the blend was the same. For the second series of PP-g-GMA, the higher the molecular weight, the higher the compatibilising efficiency.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 229 (1995), S. 1-13 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Geschmolzenes Polypropylen (PP) wurde in einem Batchmischer radikalisch mit Glycidylmethacrylat (GMA) gepfropft. Bei 200°C verläuft die Pfropfung sehr rasch und ist nach 2 bis 3 Minuten abgeschlossen. Die Pfropfausbeute beim ausschließlichen Einsatz von GMA ist niedrig und kann in Gegenwart von Styrol als Comonomerem erhöht werden, wobei auch der Kettenabbau des PP verringert wird. Die während der Pfropfung gebildeten Mengen an homo- und copolymerem GMA wurden bestimmt. Es kann angenommen werden, daß in Gegenwart von Styrol dieses zunächst mit den PP-Makroradikalen reagiert und stabilere Styryl-Radikale bildet, die dann mit GMA gepfropft werden. Die Geschwindigkeit dieser Reaktion ist sehr viel größer als die der Reaktion von GMA mit PP-Makroradikalen. Im Gegensatz zu der über einen Charge-Transfer-Komplex ablaufenden Pfropfung von Mischungen aus Maleinsäureanydrid und Styrol folgt die Pfropfung von GMA in Gegenwart von Styrol einem statistischen Copolymerisationsprozeß.
    Notes: This paper concerns free-radical grafting of glycidyl methacrylate (GMA) onto polypropylene (PP) in the molten state carried out in a batch mixer. This free-radical grafting proceeds very rapidly as it goes to completion within two to three minutes at 200°C. The grafting yield of GMA alone is low and it is greatly enhanced upon addition of styrene as a second monomer with a reduced chain degradation of PP. Homopolymer and copolymer of GMA formed during grafting were quantified. It is suggested that in the presence of styrene, the dominating grafting mechanism is that styrene reacts with the PP macroradicals to form more stable styryl macroradicals which then react with GMA to form GMA-grafted PP. The rate of this reaction is much greater than that between the PP macroradicals and GMA. Unlike grafting of mixtures of maleic anhydride and styrene, which is dictated primarily by formation of a charge transfer complex, free-radical grafting of GMA in the presence of styrene follows a random copolymerization process.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 665-675 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The transesterification reaction of poly[ethylene-co-(vinyl acetate)] (EVA) with 1-octanol was studied in the molten state by the use of a batch mixer (Haake Rheocord) as the reactor. The conversion of the vinyl acetate group into the vinyl alcohol group was determined by Fourier transform infrared spectroscopy (FTIR). Several organometallic compounds were used as catalysts, of which tin-based compounds, such as dibutyltin dilaurate and dibutyltin oxide, showed the highest activities. Experimental results suggested that the real catalyst is an intermediate product (dialkoxide) formed between an organotin compound and the reactive alcohol. This was confirmed by examining the interaction between a tin compound and an alcohol with the help of different techniques like infraed spectroscopy, high-performance liquid chromatography and mass balance. Finally, a mechanism for the transesterification in the presence of an organotin compound as catalyst was proposed, suggesting that the overall reaction rate is proportional to the concentrations of the ester and the alcohol, and to the square root of the catalyst concentration. This was fully supported by kinetic studies.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 97-107 
    ISSN: 0887-624X
    Keywords: transesterification ; interfaces ; diffusion ; mixing ; solvent effect ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This article presents a unique example dealing with how chemical reactions between immiscible polymers in the melt behave differently than they would do in solution. Specifically, a model reaction was chosen: the transesterification between poly(ethylene-co-methyl acrylate) (EMA) and polystyrene mono-hydroxylated at the chain end (PSOH). It was carried out in the melt in a batch mixer. The overall rate of this reaction has a similar dependence of temperature, composition of reactants, and the nature and concentration of catalyst as in solution. The reactivity of PSOH decreases drastically with increasing molecular weight, and it becomes very weak when the molecular weight exceeds 8000 g/mol. As opposed to a reaction in solution or in a homogeneous melt, mechanical mixing increases the reaction rate since it generates interfacial area and reduces the diffusion length. The EMA-g-PS graft copolymer formed at the interfaces reduces the interfacial tension, and increases the miscibility of the reaction mixture. However, its occupation of the interfaces reduces contact between the reactive moieties, thus decreasing the overall reactivity. More importantly and much to our surprise, adding 1 to 2 wt % of an inert solvent increased greatly the overall reaction rate. While an increased interfacial mixing and diffusion by the presence of minor amounts of solvent are thought to be the major factors contributing to the drastic increase in reactivity, numerous questions still remain. Nevertheless, this study clearly showed that as opposed to a reaction in solution, mechanical mixing and the presence of minor amounts of solvent are two additional and critical means to control chemical reactions between immiscible polymer melts. © 1995 John Wiley & Sons, Inc.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1053-1063 
    ISSN: 0887-624X
    Keywords: free radical grafting ; polypropylene ; glycidyl methacrylate ; styrene ; maleic anhydride ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The free radical grafting reactivity of glycidyl methacrylate (GMA) onto polypropylene (PP) in the molten state is low. This article shows that adding styrene as a second monomer (or comonomer) increases both the rate and yield of GMA grafting and reduces PP chain scission. The proposed mechanism is that when St is added to the PP/GMA/peroxide grafting system, St reacts first with PP macroradicals to form stable styryl macroradicals. These latter then react (or copolymerize) with GMA to form GMA grafted PP. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1053-1063, 1998
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2763-2774 
    ISSN: 0887-624X
    Keywords: free radical grafting ; glycidyl methacrylate ; polyethylene ; styrene ; reactive extrusion ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Glycidyl methacrylate (GMA) is a very useful monomer as it bears an epoxy group which is capable of reacting with various other functional groups. However, its melt free radical grafting reactivity onto a polymer backbone is low. In this study, we show that the use of styrene (St) as a comonomer greatly promotes both GMA's grafting yield and grafting rate onto polyethylene (PE). It is proposed that, in the presence of St, the dominant mechanism of the free radical grafting of GMA onto PE is that St reacts first with PE secondary macroradicals and the resulting styryl macroradicals then copolymerize with GMA leading to grafted GMA. We also show that the contribution of St is not related to an improved solubility of GMA in the molten PE. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 2763-2774, 1998
    Additional Material: 20 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3453-3464 
    ISSN: 0887-624X
    Keywords: quaternization ; poly(vinylpyridines) ; alkyl halide ; kinetics ; steric hindrance ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Quaternization reactions of poly(vinylpyridines) with alkyl halides show retardation in excess of that predicted by the classical second-order kinetics. Based on the classical collision and transition state theories, a kinetic model has been developed to quantify such retardation, in which the overall reaction rate is characterized by a rate constant k0 of the intrinsic reactivity between a pyridyl group and an alkyl halide group, and by a steric hindrance effect parameter α. The latter accounts for the degree to which the rate of collisions of reactants is reduced, or to which the freedom of movement of the reactants in the transition state is restricted as the reaction proceeds. The resulting kinetic expression has been validated using experimental results reported in the literature and those of our own. The functional dependence of k0 and α values on the nature of poly(vinylpyridines) and that of alkyl halides is explained. Other factors affecting k0 and α, including changes in macromolecular dimensions and/or in the distribution of residue environment, quality of solvent, and reaction temperature, are discussed. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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