Measurement of the Isothermal Volume Dilation Accompanying the Unilateral Extension of Rubber

1959 ◽  
Vol 32 (2) ◽  
pp. 428-433
Author(s):  
Fred G. Hewitt ◽  
Robert L. Anthony

Abstract The fractional increase in volume accompanying the isothermal extension of soft gum rubber was measured for four rubber samples at mean extensions of 14, 33, and 51%. The chain molecular weights Mc of the four samples were 5500, 5100, 4400, and 3000, with an estimated uncertainty of about 10% in each value of Mc. The observed fractional increase in volume ranged from 3.2×10−5 to 142×10−5, the latter value being observed for the sample of lowest chain molecular weight and at the extension of 51%. The experimental results for each sample have been represented by theoretical curves based on Gee's expression for the fractional increase in volume as a function of the sample extension. The theoretical curves exhibit good agreement with those of Gee, Stern, and Treloar. The process of fitting the theoretical curves to the experimental points constituted a determination of Young's modulus E for each rubber specimen. As a check on the experimental results, and also on the theory employed, determinations of E were also made by two additional methods, namely, from rough stess-strain curves, and from the relation E=3γρRT/Mc. With one exception, the internal agreement between the three determinations of E for the four different samples was satisfactory. The exception noted can probably be ascribed to the use of too small a value of Mc for the sample of lowest chain molecular weight.

2018 ◽  
Vol 233 ◽  
pp. 00025
Author(s):  
P.V. Polydoropoulou ◽  
K.I. Tserpes ◽  
Sp.G. Pantelakis ◽  
Ch.V. Katsiropoulos

In this work a multi-scale model simulating the effect of the dispersion, the waviness as well as the agglomerations of MWCNTs on the Young’s modulus of a polymer enhanced with 0.4% MWCNTs (v/v) has been developed. Representative Unit Cells (RUCs) have been employed for the determination of the homogenized elastic properties of the MWCNT/polymer. The elastic properties computed by the RUCs were assigned to the Finite Element (FE) model of a tension specimen which was used to predict the Young’s modulus of the enhanced material. Furthermore, a comparison with experimental results obtained by tensile testing according to ASTM 638 has been made. The results show a remarkable decrease of the Young’s modulus for the polymer enhanced with aligned MWCNTs due to the increase of the CNT agglomerations. On the other hand, slight differences on the Young’s modulus have been observed for the material enhanced with randomly-oriented MWCNTs by the increase of the MWCNTs agglomerations, which might be attributed to the low concentration of the MWCNTs into the polymer. Moreover, the increase of the MWCNTs waviness led to a significant decrease of the Young’s modulus of the polymer enhanced with aligned MWCNTs. The experimental results in terms of the Young’s modulus are predicted well by assuming a random dispersion of MWCNTs into the polymer.


1941 ◽  
Vol 14 (3) ◽  
pp. 580-589 ◽  
Author(s):  
G. Gee ◽  
L. R. G. Treloar

Abstract As high elasticity is a property possessed only by substances of high molecular weight, it is of interest to enquire into the relation between the elastic properties of a highly elastic material such as rubber and its molecular weight. An investigation on these lines has been made possible through the work of Bloomfield and Farmer, who have succeeded in separating natural rubber into fractions having different average molecular weights. The more important physical properties of these fractions have been examined with the object of determining which of the properties are dependent on molecular weight and which are not. Fairly extensive observations were made on the fractions from latex rubber referred to as Nos. 2, 3 and 4 by Bloomfield and Farmer, and some less extensive observations were carried out on the less oxygenated portion of fraction No. 1 obtained from crepe rubber (called hereafter 1b) . Before considering these experimental results, and their relation to the molecular weights of the fractions, it will be necessary to refer briefly to the methods used for the molecular-weight determinations, and to discuss the significance of the figures obtained.


1986 ◽  
Vol 71 ◽  
Author(s):  
I. Suni ◽  
M. Finetti ◽  
K. Grahn

AbstractA computer model based on the finite element method has been applied to evaluate the effect of the parasitic area between contact and diffusion edges on end resistance measurements in four terminal Kelvin resistor structures. The model is then applied to Al/Ti/n+ Si contacts and a value of contact resistivity of Qc = 1.8×10−7.Ωcm2 is derived. For comparison, the use of a self-aligned structure to avoid parasitic effects is presented and the first experimental results obtained on Al/Ti/n+Si and Al/CoSi2/n+Si contacts are shown and discussed.


1998 ◽  
Vol 507 ◽  
Author(s):  
M. Zeman ◽  
R.A.C.M.M. Van Swaaij ◽  
E. Schroten ◽  
L.L.A. Vosteen ◽  
J.W. Metselaar

ABSTRACTA calibration procedure for determining the model input parameters of standard a-Si:H layers, which comprise a single junction a-Si:H solar cell, is presented. The calibration procedure consists of: i) deposition of the separate layers, ii) measurement of the material properties, iii) fitting the model parameters to match the measured properties, iv) simulation of test devices and comparison with experimental results. The inverse modeling procedure was used to extract values of the most influential model parameters by fitting the simulated material properties to the measured ones. In case of doped layers the extracted values of the characteristic energies of exponentially decaying tail states are much higher than the values reported in literature. Using the extracted values of model parameters a good agreement between the measured and calculated characteristics of a reference solar cell was reached. The presented procedure could not solve directly an important issue concerning a value of the mobility gap in a-Si:H alloys.


1973 ◽  
Vol 95 (4) ◽  
pp. 535-538 ◽  
Author(s):  
J. C. Lin ◽  
R. Greif

The absorption of a vibrational-rotational band has been studied and the contribution from the first hot band has been included. A specific application has been made to carbon monoxide and good agreement with experimental results has been obtained.


PEDIATRICS ◽  
1972 ◽  
Vol 50 (5) ◽  
pp. 688-692
Author(s):  
Anatole S. Dekaban ◽  
Kenton R. Holden ◽  
George Constantopoulos

Repeated fresh plasma or whole blood transfusions were given to five patients with either Hurler, Hunter, or Sanfilippo types of mucopolysaccharidosis. Clinical observations and total 24-hour urinary AMPS and their composition and molecular weight distribution were determined before, during, and after transfusions. The two patients who received plasma transfusions showed no noticeable change in the amount of AMPS excreted; of the three patients who received whole blood transfusions, two had slightly less excretion of AMPS while the third showed no difference. The AMPS in the CSF were measured in one patient before and after blood transfusions and found to be unchanged; likewise, the determination of molecular weights in the isolated AMPS was virtually identical. In the patients studied, the transfusions caused no demonstrable difference in the patients' clinical condition.


2010 ◽  
Vol 3 (2) ◽  
pp. 47-60
Author(s):  
Alexey V. Starov

In this paper, analysis of existing methods application of criterial description of ignition conditions and combustion break-out for summarizing of experimental results is carried out. Experimental results are obtained at investigations of hydrogen combustion in combustor with high supersonic speed of airflow. For these conditions selection of several criterions was substantiated and they have a good agreement with new experimental results. At the same time complexity of determination of experimental physical parameters, which are included in criterions, do not allow confidently to apply them for prediction of steady-state combustion limits. Therefore further accumulation of experimental data and development of measurement methods are necessary for accurate criterions obtaining.


1987 ◽  
Vol 52 (5) ◽  
pp. 1235-1245 ◽  
Author(s):  
Petr Štěpánek ◽  
Zdeněk Tuzar ◽  
Čestmír Koňák

The response of quasielastic light scattering to the polydispersity of scattering objects has been investigated. A new method of the polydispersity index determination has been suggested, suitable for the range 1.02 ⪬ Mw/Mn ⪬ 2.0 and consisting in the measurement of the dependence of the apparent decay time on the correlator sampling time. The polydispersity index can be determined by comparing these dependences with the theoretical ones obtained using correlation curves simulated for various values of the polydispersity index, assuming lognormal and Schulz-Zimm distributions of molecular weights. The test measurements on polystyrene standards having molecular weights in the range 9 103 – 20.6 106 give polydispersity index values Mw/Mn that are in a good agreement with those given by the manufacturer. The polydispersity index for polystyrene having the molecular weight Mw = 20.6 106 thus determined was Mw/Mn = 1.35.


1978 ◽  
Vol 56 (11) ◽  
pp. 1569-1574
Author(s):  
Nga Ho-Duc

Theoretically we can determine the disordered or ordered structure of polypeptides and their dimensions in dilute solutions from hydrodynamic properties. We have presently a wealth of theories for random coil chains and a limited but sufficient number of theories for ordered chains for interpreting experimental results.Viscosity data for seven poly(γ-benzyl-L-glutamate) samples in 1,2-dichloroethane at 25 °C are analyzed and the length per monomeric residue (h) is calculated according to the equivalent ellipsoid approach. The degree of flexibility or rigidity is characterized by calculating Ns, the number of monomer units in a rigid segment or a Kuhn statistical segment; the determination of Ns is made by applying Yamakawa and Fujii's equation modified by Vitovskaya and Tsvetkov.Values obtained for h assuming the solute molecule to be a rigid, stiff chain, range between 1.3 to 2 Å. One notices that the h value close to 1.5 Å is found for the three following molecular weights: 1.8 × 105, 1.7 × 105, and 1.5 × 105. They are, in fact, the samples having a length in good quantitative agreement with that of the rigid segment determined by the method of Vitovskaya and Tsvetkov. This rigid segment corresponds to a sample of 700 ± 100 monomer units.The analysis of the experimental data of poly(γ-benzyl-L-glutamate) in dichloroacetic acid indicates that, in addition to the formation of hydrogen bonds, other interactions between the polypeptide and the solvent are present.In summary, we may conclude that the study of the helix–coil transition using hydrodynamic measurements is judged satisfactory but the determination of characteristic dimensions used to describe exactly the conformation of the macromolecule is somewhat ambiguous. One major problem is the degree of flexibility encountered with high molecular weight chains. However, to get around this difficulty, we propose, according to our results, a method which consists in determining the number of monomer units within a rigid segment from the different values found for h and then the dimensions from the samples for which the chain length is in good agreement with that of a rigid segment thus determined.


1943 ◽  
Vol 16 (3) ◽  
pp. 493-508
Author(s):  
Paul J. Flory

Abstract Experimental methods for fractionating polyisobutylene and for determining osmotic pressures have been described. The ratio π/c of osmotic pressure to concentration has been found in the case of cyclohexane solutions of polyisobutylene to vary nonlinearly with concentration, contrary to recent theories advanced by Huggins and the writer. The slope of this relationship appears to be independent of molecular weight. Reliable methods for extrapolating π/c to c=0 have been established, enabling the determination of absolute molecular weights with satisfactory precision up to values of about 1,000,000. Molecular weights of polyisobutylenes calculated from Staudinger's equation are too low; the discrepancy is more than ten-fold at high molecular weights. On the basis of data for carefully fractionated samples covering a two-hundred-fold molecular weight range, the intrinsic viscosity is found to be proportional to the 0.64 power of the molecular weight. This decided deviation from Staudinger's “law”cannot in this instance be attributed to nonlinear chain structure, as Staudinger has sought to do in other cases. This dependence of molecular weight on intrinsic viscosity leads to the definition of a “viscosity average”molecular weight which is obtained when the relationship is applied to heterogeneous polymers. The viscosity average is less than the weight average molecular weight, which would be obtained if Staudinger's equation were applicable, and greater than the number average obtained by osmotic or cryoscopic methods.


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