scholarly journals Interfacial rheology testing of molten polymer systems: Effect of molecular weight and temperature on the interfacial properties

2021 ◽  
pp. 107280
Author(s):  
Younes El Omari ◽  
Mohamed Yousfi ◽  
Jannick Duchet-Rumeau ◽  
Abderrahim Maazouz
2000 ◽  
Vol 19 (5) ◽  
pp. 579-589 ◽  
Author(s):  
N Sombatsompop ◽  
N.-T Intawong ◽  
N.-S Intawong

1955 ◽  
Vol 28 (1) ◽  
pp. 72-83
Author(s):  
F. M. Mebrett

Abstract In Part I of this investigation, the effect of dihydromyrcene on four vinyl polymerizing systems was studied, and it was found that this compound reduces both the molecular weight of the polymer formed and the rate of polymerization. With rubber, the results are more complicated. A method for separating the simple polymers from the graft (compound) polymers is developed. This method is based on the peculiar colloidal properties of the graft polymers. These separations show that interaction between the natural and synthetic polymers depends on the catalyst used for initiating the polymerization and, therefore, that more than simple transfer is involved. Thus, with benzoyl peroxide, numerous very short side chains are combined with the rubber, while the free vinyl polymer chain grows to approximately the length predicted from known data. With azoisobutyronitrile, on the other hand, there is little or no reaction between the rubber and vinyl component. It is suggested that the formation of these very short grafted chains in place of the expected long ones may be a general feature of rubber-polymer systems of this type.


1990 ◽  
Vol 63 (5) ◽  
pp. 734-746 ◽  
Author(s):  
Jacques Roovers ◽  
Paul M. Toporowski

Abstract In the course of work on linear and ring polybutadienes with 62% 1,2 units, a number of discrepancies were noted with data on polybutadienes of various microstructure available in the literature. For example, GNο=870 kPa for our 62% 1,2-polybutadiene. This is larger than GNο=730 kPa for a 56% 1,2-polybutadiene and GNο=550 kPa for a 78% 1,2-polybutadiene sample. The cis : trans ratio of our 62% 1,2-polybutadiene, prepared with potassium counterion, is 1 : 4, On the other hand, the cis : trans ratio of 62% 1,2-polybutadiene prepared with a modified Li catalyst is estimated to be 1 : 2. It is conceivable that the different cis : trans ratio leads to different properties at constant 1,2 content. Nevertheless, the low levels of both the cis and the trans units are not expected to cause more than minor differences in the properties of the polybutadienes. Correct values for GNο of model polymers are important for the study of the influence of the chemical structure on the melt characteristics of a polymer. For this reason, it was thought useful to reinvestigate 1,2-polybutadiene itself in some detail. The synthesis of narrow molecular-weight distribution 1,2-polybutadiene by anionic polymerization techniques has been described recently. The dilute-solution properties of 1,2-polybutadiene has been investigated. The melt rheology of two 1,2-polybutadiene samples have been studied, but no systematic study of the molecular-weight dependence of the melt properties was made. 1,2-Polybutadiene has been used as a component in block copolymers with 1,4-polybutadiene. These studies have permitted an investigation of the phase behavior of two rubbery blocks at room temperature. Poly(l,4-butadiene-graft-l,2-butadiene)s with well-defined composition and architecture have also been prepared. Hydrosilylated 1,2-polybutadiene has found use as the coupling agent for multiarm star polymer, and this method can easily be extended to the preparation of poly( l,2-butadiene-graft-l,4-butadiene). Hydrogenated 1,2-polybutadienes are prepared as model polymers for poly(l-butene). The synthesis and characterization of a series of 1,2-polybutadienes are described here. Special attention is given to low-molecular-weight polymers. The linear viscoelastic properties of the melts are also described. In the discussion, the relation between the characteristic ratio, C∞, and the plateau modulus, GNο, of a number of model polymer systems is explored.


2021 ◽  
Author(s):  
Theresia Heiden-Hecht ◽  
Stephan Drusch

AbstractOil in water emulsions are commonly stabilized by emulsifying constituents like proteins and/or low molecular weight emulsifiers. The emulsifying constituents can compete or coexist at the interface. Interfacial properties thus depend on molecular structure of the emulsifying constituents and the oil phase and the resulting molecular interactions. The present study systematically analyzed the impact of fatty acid saturation of triacylglycerides and phosphatidylcholine on the interfacial properties of a β-lactoglobulin-stabilized interface. The long-term adsorption behaviour and the viscoelasticity of β-lactoglobulin-films were analyzed with or without addition of phosphatidylcholine via drop tensiometry and dilatational rheology. Results from the present study showed that increasing similarity in fatty acid saturation and thus interaction of phosphatidylcholine and oil phase increased the interfacial tension for the phosphatidylcholine alone or in combination with β-lactoglobulin. The characteristics and stability of interfacial films with β-lactoglobulin-phosphatidylcholine are further affected by interfacial adsorption during changes in interfacial area and crystallization events of low molecular weight emulsifiers. This knowledge gives guidance for improving physical stability of protein-based emulsions in foods and related areas. Graphic abstract


Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2439
Author(s):  
Quantao Fang ◽  
Jiawei Yao ◽  
Kangmin Niu ◽  
Jun Tang ◽  
Yan Wei ◽  
...  

The molecular weight of self-emulsifying amphiphilic epoxy sizing emulsions has a big effect on the carbon fibres and interfacial properties of their composites. Novel amphiphilic epoxy sizing emulsions with four different molecular weights (7500, 11,000, 15,000 and 17,000) were successfully prepared by a self-emulsifying method and applied to improve interfacial bonding between carbon fibres (CFs) and an epoxy resin (EP). The effect of molecular weight on the quality of emulsions, the sized CFs and the interfacial properties of the CF/EP composite system were studied. The results reveal that these novel sizing emulsions exhibited strong emulsifying ability and high processability. The most favourable wettability and adequate CF surface free energy were obtained by the emulsion with a molecular weight of 7500. Compared with unsized CFs, the monofilament fibre tensile performance was remarkably improved when increasing the shape parameter from 5.08 to 7.20. The interfacial sheer strength (IFSS) of the CF/EP composite was greatly increased by 96% with the emulsion of 7500. The enhanced interfacial adhesion benefits were attributed mainly from the enhanced charge interaction between CFs and the sizing layer as well as the compatibility and the mechanical interlock between the sizing layer and the epoxy matrix.


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