Effect of Extending Oil on Viscoelastic Behavior of Elastomers

1983 ◽  
Vol 56 (4) ◽  
pp. 784-807 ◽  
Author(s):  
N. Nakajima ◽  
E. R. Harrell

Abstract For a number of years, oil-extended elastomers have been in commercial use. The obvious advantage is to dilute elastomers with less expensive oil. In addition, oil improves the processability of the elastomer. This enables the use of a higher-molecular-weight polymer, which, in turn, yields mechanical properties comparable or superior to those of a lower-molecular-weight polymer without oil extension. The viscoelastic properties of the oil-elastomer mixtures at a wide range of concentration and temperature offer information useful for understanding elastomer processability. The viscoelastic properties of such systems are also most sensitive manifestations of the polymer chain structure and, therefore, they represent fundamental characteristics of a given elastomer sample. In this work, two samples of ethylene-propylene copolymer differing in chain structure were selected. The oil-elastomer mixtures were prepared for polymer concentration in the range of 2.5–100%. The viscoelastic properties have been measured in the temperature range of 30–150°C. The frequency range was 10−1–102 rad/s and in some cases −2–102 rad/ s. The superposition principles have been examined with these data for both the temperature and concentration dependence.

1996 ◽  
Vol 69 (1) ◽  
pp. 73-80 ◽  
Author(s):  
N. Nakajima

Abstract Dynamic mechanical measurements were performed with styrene-butadiene-styrene (SBS) block copolymers, Kraton D-1101 and D-l 102. Isochronal data were obtained from −130 to 85°C in the tensile mode at 1 Hz and from 60 to 160°C in the shear mode at 1 rad/s. The isothermal measurements were also performed at 60, 90, 120, 140, and 160°C in the frequency range of 0.0316 to 100 rad/s. The results suggest that the two polymers have different morphologies although the styrene content and the diblock content are about the same for both polymers. Kraton D-1101, which has 1.5 times higher molecular weight, has 3–5 times higher rubbery modulus, compared to D-1102. The lower molecular weight polymer, D-1102, appears to have a larger amount of the mixed phase at the boundary. This is suggest by the lower temperature of the “domain disruption”, Tdd and the higher magnitude of tan δ at Tdd. This explains the difference in the rubbery moduli of the two polymers.


2018 ◽  
Vol 54 (5A) ◽  
pp. 99
Author(s):  
Nguyen Vu Viet Linh

This research investigated the effects of polymer concentration, molecular weight polymer and type of polymer on the morphology of electrosprayed microparticles by Scanning Electron Microscopy. Electrospraying process has been studied to produce nano- and micro- particles for drug carrier application because of high loading capacity and high encapsulation efficiency. Controlling morphology and structure of electrosprayed particles can decide the release of drug from these particles. Particles were hollow and wrinkled semi-spheres as using low polymer concentration while wrinkled spheres as using higher polymer concentration. The electrosprayed particles obtained spherical morphology when the polymer concentration is high enough to generate significant chain entanglements. The results also indicated that high molecular weight polymer could produce spherical microspheres, even with low polymer concentration. The electrospraying process fabricated the microspheres from biodegradable PLA and PCL for drug carrier application. 


1970 ◽  
Vol 92 (3) ◽  
pp. 411-418 ◽  
Author(s):  
W. D. White ◽  
D. M. McEligot

Data are presented for the flow of deionized water solutions of linear, unbranched polymers—Separan AP-30, Polyox WSR-35 and Polyox WSR-301, and mixtures of the latter two in a 0.0235 in. tube. The Reynolds numbers vary from about 1200 to about 12,000. Measurements were made at 4 deg C and near room temperature. Occurrence of transition is confirmed by oscillograph traces and pressure ratio calculations in addition to the usual “break” on a friction factor-Reynolds number graph. From the calibration data, it appears that for small tubes there is a critical parameter, such as molecular weight or polymer length, below which transition occurs as for water, but above which the transition Reynolds number depends on polymer concentration. The low and high polymers were mixed to vary molecular weight distribution of samples. It was found that the higher molecular weight polymer dominates the transition process, but in the turbulent regime the effects are roughly additive.


2020 ◽  
Vol 18 (1) ◽  
pp. 75-92
Author(s):  
Lizcano Nino J.C ◽  
Ferreira Vitor Hugo de Sousa ◽  
Moreno Rosangela B. Z. L

Polymer Flooding has become one of the most implemented EOR techniques, due to three factors: First, Polymer flooding has expanded the range of the screening criteria parameters. Second, this EOR method is more effective than water injection, while handling water management issues in high water-cut reservoirs. Nevertheless, polymer retention can turn a viable technical project into an uneconomical one. Polymer loss due to retention is an inevitable phenomenon, which happens during injection processes. The development of experimental analysis aiming to minimize or reduce polymer loss from the displacing fluid bank is beneficial to broaden the application of this CEOR method. This experimental work evaluated the injection schemes aiming to reduce polymer retention in porous media. The approach consisted of injecting less-concentrated polymer banks followed for the main polymer bank designed for mobility control. An experimental methodology to quantify polymer retention due to each injected polymer bank, cumulative polymer retention, resistance factor, residual resistance factor and inaccessible pore volume (IPV) was developed. The measurement process was based on the injection of 20 PV polymer banks at a constant flow rate of 1ml/min at 25°C, separated by 30 PV brine banks. Two HPAM with molecular weights of 6-8 million and 20 million Daltons using 350mD and 5000 mD sandstone cores were tested, respectively. The HPAM solutions considering a Colombian field (0.7% NaCl) and seawater (3.5% TDS) salinities were prepared. All rock samples were previously submitted to the injection of 50 PV for preventing fines migration. Two injection schemes with variable polymer concentrations were performed: The first one in which the polymer concentration increased in each successive bank, and the second one in which the concentration decreased. HPAM concentration solutions from 50 ppm to 2000 ppm were sequentially used in both injection schemes. By comparing the results of these two schemes, the effect of the injection of the less-concentrated polymer solutions was evaluated. For the increasing concentration experiments, cumulative retention values of 175.7 μg/g and 58.9 μg/g were calculated for the low-molecular weight polymer and the high-molecular weight polymer, respectively. While comparing with decreasing concentration experiments, for the high-molecular weight HPAM a 19% of retention reduction was evidenced, but no retention reduction was observed for the low-molecular weight one. The results indicate that different retention mechanisms are strongly dependents on the absolute permeability of the samples. Additionally, IPV values of 0.5 PV and 0.25 PV were calculated using low and high permeability samples, respectively. There was no linear relation between the absolute permeability reduction and the polymer concentration of the first bank injected into the sample. The novelty of this work is to use sacrificial banks of less-concentrated HPAM solutions as a reducing retention agent for the polymer bank designed for mobility control.


2008 ◽  
Vol 55-57 ◽  
pp. 905-908 ◽  
Author(s):  
N. Jintakanon ◽  
Pakorn Opaprakasit ◽  
Atitsa Petchsuk ◽  
Mantana Opaprakasit

ontrolled-release materials for urea are prepared by spray coating urea granulates with lactic acid based homo- and co-polymers solutions. Percent coating as a function of polymer types, molecular weight, polymer concentration, and dose applications are examined by gravimetric analysis. Percentage of urea dissolution in water of the coated fertilizer is measured by monitoring refractive index of the solutions. Morphology of the polymer coating surfaces is revealed by Scanning Electron Microscopy (SEM). It was found that an amount of cracks and pin-holes, which is dependent on polymer types and molecular weight, plays a significant role in controlling the rate of urea release. Results from urea dissolution test also suggests that the synthesized poly(lactic acid-co-ethylene terephthalate) show urea-holding efficiency comparable to that of commercial PLA, despite its much lower molecular weight, indicating that the copolymer is potentially suitable for this specific application.


1995 ◽  
Vol 12 (3) ◽  
pp. 259-265 ◽  
Author(s):  
S. Millot ◽  
J.L. Loubet ◽  
J.M. Georges

An extensive study on the determination of the 'hydrodynamic' layer thickness of polymer solutions and melt polymers was conducted with a surface force apparatus. For different concentrations and polymer molecular weights, a 'hydrodynamic layer' of fluid was detected on each solid surface which did not contribute to the flow. These thicknesses, denoted as LH, are compared to the characteristic polymer dimensions and the hydrodynamic (RH) and gyration (Rg) radii. It appears that in contrast to the molecular weight, polymer concentration has little effect on the relative hydrodynamic layer thickness (LH/2RH, LH/2Rg). Indeed, this ratio indicates that two coils of low molecular weight and one coil of high molecular weight are 'immobile' on the solid surfaces. The mechanism responsible could be entanglement of the free (unattached) chains in the bulk with immobilized chains on the surface.


1975 ◽  
Vol 48 (4) ◽  
pp. 548-557 ◽  
Author(s):  
G. R. Cotten

Abstract 1. A direct correlation between bound rubber content and molecular weight of soluble polymer was found for a wide range of carbon black samples and processing conditions in SBR. 2. No significant polymer degradation occurred during the ineorporation of carbon black into SBR rubber. 3. A theory was proposed to explain the observed changes in viscosity and extrusion shrinkage of rubber stocks. This theory is based on the concept of occluded rubber which is rich in high molecular weight polymer and behaves as a part of filler volume during viscous flow.


2013 ◽  
Vol 734-737 ◽  
pp. 2549-2552
Author(s):  
Jiu Zhou Sun ◽  
Chang Bin Wang ◽  
Liang Kan ◽  
Ze Hua Wang

The laboratory evaluation studied the matching relationship between different concentration polymer solution and the formation permeability,and also the matching relationship between different molecular weight polymer solution and the formation permeability. The influences on the solution viscoelasticity,which were caused by the polymer concentration and the molecular weights,were analysed by the laboratory evaluation tests on the viscoelasticity of the polymer solution.


1982 ◽  
Vol 47 (03) ◽  
pp. 197-202 ◽  
Author(s):  
Kurt Huber ◽  
Johannes Kirchheimer ◽  
Bernd R Binder

SummaryUrokinase (UK) could be purified to apparent homogeneity starting from crude urine by sequential adsorption and elution of the enzyme to gelatine-Sepharose and agmatine-Sepharose followed by gel filtration on Sephadex G-150. The purified product exhibited characteristics of the high molecular weight urokinase (HMW-UK) but did contain two distinct entities, one of which exhibited a two chain structure as reported for the HMW-UK while the other one exhibited an apparent single chain structure. The purification described is rapid and simple and results in an enzyme with probably no major alterations. Yields are high enough to obtain purified enzymes for characterization of UK from individual donors.


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