Search results for "shear"

Friction between Polymer Brushes in Good Solvent Conditions:  Steady-State Sliding versus Transient Behavior

2003

Previous molecular dynamics simulations of friction between polymer brushes in relative sliding motion [Kreer, T.; Muser, M. H.; Binder, K.; Klein, J. Langmuir 2001, 17, 7804] are extended beyond steady-state conditions. We study two different protocols:  (i) stop and return and (ii) stop and go. In protocol (i), the relative, lateral motion between the two surfaces is stopped abruptly and reimposed opposite to the initial direction after the system could relax for some time. Protocol (ii) is similar except that the sliding direction is maintained. In the constant-velocity steady state, the average lateral extension lc of the polymers is found to be a power law of the sliding velocity v, na…

Solidification behavior of the theta system 2-propanol/poly(n-butyl methacrylate)

1995

Thermoreversible gelation of the system 2-propanol/poly (n-butyl methacrylate) — as detected by D'SC or dielectric experiments — does not manifest itself in a straightforward manner in the dynamic-mechanical properties. Its occurrence can, however, be seen in many ways: i) For constant composition of the system and a reference temperature lower than Tgel, the storage modulus G′ is larger than the loss modulus G″ in the glass transition zone of the master curve and both vary in an almost parallel manner with the angular frequency ω over almost two decades (whereas this feature is normally found for other gelling systems within the rubber plateau or the flow region). ii) The entanglement mole…

Melt Strength and Extensibility of High-Density Polyethylene

1984

The extensional flow of polymer melts has been extensively studied because of its importance in many technological processing operations and, from a more fundamental point of view, because the tensile properties of the polymer melts cannot be correlated directly with shear viscosity behavior.1–5

The non-isothermal rheological behaviour of molten polymers: Shear and elongational stress growth of polyisobutylene under heating

1981

Data of stress growth under both shear and elongational kinematics have been taken in presence of heating temperature ramps on a commerical polyisobutylene.

1988

Phase diagrams were calculated for flowing solutions of polystyrene in trans-decahydronaphthalene assuming that the energy (Es) stored in the sheared state has to be added to the Gibbs energy of mixing; Es is computed from viscometric data (flow curves). The resulting phase diagrams exhibit two maxima in most of the cases instead of only one for the stagnant solutions. A comparison with experimental data (Part 1) shows that the calculated demixing behaviour agrees well for moderate shear rates and concentrations of the polymer. Deviations in the semidilute region, particularly for higher values, are a consequence of the fact that so far no reliable theoretical relation has been given for th…

Combined Effects of Pressure and Shear on the Phase Separation of Polymer Solutions

1998

Experimental information available in the literature on the phase separation behavior of the system trans-decalin/polystyrene as a function of pressure and shear rate for different molar masses M o...

Thermo-Mechanical Degradation of LDPE-Based Nanocomposites

2007

Thermo-mechanical degradation of LDPE-based nanocomposites was studied by mainly investigating the rheological properties. For all of the investigated processing conditions, the viscosity of the nanocomposites was higher than that of the pure-LDPE matrix, but on increasing the severity of the mixing conditions, the difference between the viscosity of the nano-filled polymer and that of the pure LDPE decreased. The X-ray traces of the nanocomposites suggest that intercalation has been achieved during the melt, when less-severe processing conditions were used. At severe processing conditions (longer mixing time, high temperature and shear stress) the thermo-mechanical degradation was accelera…

Shear induced mixing/demixing: blends of homopolymers, of homopolymers plus copolymers, and blends in solution

2000

Shear may shift the phase boundary towards the homogeneous state (shear induced mixing, SIM), or in the opposite direction (shear induced demixing, SID). SIM is the typical behavior of mixtures of components of low molar mass and polymer solutions, SID can be observed with solutions of high molar mass polymers and polymer blends at higher shear rates. The typical sequence with increasing shear rate is SIM, then occurrence of an isolated additional immiscible area (SLD), melting of this island into the main miscibility gap, and finally SIM again. A three phase line originates and ends in two critical end points. Raising pressure increases the shear effects. For copolymer containing systems S…

Phase behavior and elastic properties of a slightly crosslinked liquid crystalline main-chain polymer

1990

A liquid crystalline main-chain polymer was slightly crosslinked by a reaction withα, ω-difunctionalized oligo-siloxanes. Crosslinking does not disturb the liquid crystalline phases, which are identified by x-ray measurements as smecticB and smecticA phases. Measurements of the elastic properties of the crosslinked sample show rubber-like elasticity, even in the liquid crystalline phases. A difference of 7 K was found between cooling and heating for the smecticA/isotropic transition from DSC and mechanical measurements.

1991

A new rotational viscometer is presented which can be operated up to 2 000 bar and a maximum shear stress of 420 Pa. It allows, for the first time, to investigate the non-Newtonian flow behaviour of moderately concentrated polymer solutions. Results of measurements with two representatives of the system 2-propanol/poly(butyl methacrylate) with weight-average molecular weights Mw = 520 000 and Mw = 2 050 000, and ratios of weight- to number-average molecular weights Mw/Mn = 1,08 and Mw/Mw = 1,23, resp. in the region of moderate polymer concentrations are reported. For a ca. 7 wt.-% solution of the higher-molecular-weight polymer one obtains viscometric relaxation times τ0 varying from 1 to 1…