scholarly journals Counterion adsorption theory of dilute polyelectrolyte solutions: Apparent molecular weight, second virial coefficient, and intermolecular structure factor

2012 ◽  
Vol 137 (3) ◽  
pp. 034902 ◽  
Author(s):  
M. Muthukumar

1968 ◽  
Vol 110 (2) ◽  
pp. 243-250 ◽  
Author(s):  
A. J. Haydon ◽  
A. R. Peacocke

1. The lysine-rich fraction (Ia+Ib, or f1) of calf thymus histones was isolated as the sulphate by acid extraction. 2. Sedimentation-equilibrium measurements with interference optics showed that this fraction was monodisperse with a molecular weight of 19500±2000. 3. The ‘apparent molecular weight’ calculated from the sedimentation-equilibrium studies varied markedly with concentration. The large second virial coefficient implied by such variation was attributed to the very high charge/mass ratio of this relatively small protein. Estimates of the charge were made from the values of this virial coefficient. 4. The very large value of the virial coefficient explains anomalies in the earlier reports of the molecular weight of this histone and also why the z-average molecular weight can appear to be lower than the weight-average molecular weight. 5. The differences of the specific refractive increments, and the partial specific volumes, between dialysed and undialysed solutions of this histone fraction could also be attributed to its high molecular charge, which was estimated from these differences and agreed, within the expected limits, with the value deduced from the second virial coefficient. 6. Sedimentation-velocity measurements combined with the known molecular weight imply that lysine-rich histone has a high frictional ratio and an extended shape. Optical-rotatory-dispersion measurements indicated that it had a low helical content.



2008 ◽  
Vol 86 (6) ◽  
pp. 503-511 ◽  
Author(s):  
Stephanie Beck-Candanedo ◽  
David Viet ◽  
Derek G Gray

The partitioning behaviour of dye-labeled dextrans of high molecular weight in aqueous suspensions of native cellulose nanocrystals was studied. Cellulose concentrations lie in the isotropic–nematic coexistence region. Blue dextrans of various molecular weights and degrees of substitution of dye molecules (anionic Cibacron blue 3G-A) were investigated. Increasing the total concentration of blue dextran and degree of dye substitution led to increasing partition coefficients. Increasing dextran molecular weight resulted in higher partition coefficients, in agreement with theory. Partition coefficients were larger than predicted theoretically using a second virial coefficient approximation. Electrostatic and entropic contributions to the partition coefficient of blue dextran are discussed. Dextrans labeled with neutral fluorescein isothiocyanate did not partition preferentially in this system.Key words: partition coefficient, cellulose nanocrystals, dextrans, degree of substitution, polyelectrolyte.



2002 ◽  
Vol 106 (21) ◽  
pp. 5500-5505 ◽  
Author(s):  
A. Striolo ◽  
J. Ward ◽  
J. M. Prausnitz ◽  
W. J. Parak ◽  
D. Zanchet ◽  
...  


1962 ◽  
Vol 35 (4) ◽  
pp. 908-917 ◽  
Author(s):  
G. V. Schulz ◽  
A. Mula

Abstract Natural rubber can be brominated in dilute cyclohexane solution, whereby the molecular weight, corresponding to the bromine content, increases. For brominated rubber, increasing bromine content makes cyclohexane an increasingly poorer solvent, which is shown by a contraction of the molecule coils and a decrease in the second virial coefficient. Quantitative results were obtained through viscosity and light scattering measurements. Cyclohexane solutions of brominated rubber containing about 43% bromine have a θ point at room temperature. Here the second virial coefficient is zero and the coil has an ideal Gaussian density distribution. In this state the coil diameter is about 1.6 times bigger than for completely free rotation. A comparison of these data with X-ray low angle scattering could yield a quantitative measure of possible molecular branching. Brominated rubber with about one bromine per isoprene residue is a good starting material for the preparation of electron-microscope samples which can be used for the determination of the molecular weight distribution in rubber. The value of the weight average degree of polymerization determined by an electron microscope is in agreement with that determined through (1) light scattering and (2) ultracentrifuge and diffusion measurements. The molecular inhomogeneity of our sample is of the order of 0.5.



1993 ◽  
Vol 46 (6) ◽  
pp. 929 ◽  
Author(s):  
K Kiyosawa

The osmotic pressures of aqueous solutions of small non-electrolytes, namely ethane-1,2-diol, propane-1,2,3-triol, sucrose and raffinose , were found to be expressible by quadratic equations of the molar concentration, which indicate that these aqueous systems involve no term higher than the second virial coefficient A2. Analysis has shown that A2 mainly does not arise from non-ideality of the aqueous solutions, but its magnitude depends on the partial molar volume of the solute, more precisely on the molecular weight or van der Waals radius or volume of the solute in the aqueous solution.



1985 ◽  
Vol 17 (4) ◽  
pp. 657-660 ◽  
Author(s):  
Lina Zhang ◽  
Dajian Qiu ◽  
Renyuan Qian


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