A method for analyzing non-Newtonian blood viscosity data in low shear rates

Viscosity measurements were made using a coaxial rotating cylinder viscometer for blood having various volume fractions of red cells. A method is described for analyzing non-Newtonian blood viscosity in low shear rates by taking account of an increase or a decrease in size of red cell aggregates induced by shear. Our results are compared with empirical formulae presented by Scott Blair, Weaver-Evans-Walder and Thurston.     

A modified graphical method for determination of equilibrium constants

A modification is described of the method of Dixon (1965) for determining equilibrium constants (K) of combinations of the type A+Bright harpoon over left harpoonAB. The method obviates drawing of a tangent to the curve at the origin.     

Hydrodynamics of non-Newtonian liquids in external-loop airlift bioreactors

In order to obtain further information on the behaviour and optimal design of external-circulation-loop airlift bioreactors, the liquid circulating velocity was studied using highly viscous pseudoplastic solutions of starch and antibiotic biosynthesis liquids of Penicillium chrysogenum, Streptomyces griseus, Streptomyces erythreus, Bacillus licheniformis and Cephalosporium acremonium. Measurements of liquid circulation velocity were made in laboratory and pilot plant external-loop airlift bioreactors, under various conditions concerning gas flow rate, riser liquid height at constant downcomer height, A _D /A _R ratio, using the impulse-response technique. It has been found that these parameters had a significant effect on liquid circulation velocity together with the apparent viscosity and dry weight of the solid phase in the biosynthesis liquids. For the tested liquids, the superficial liquid velocity in the riser section of an external-loop airlift bioreactor may be described by the following equation: where the exponents and the constant c take different values depending on the liquid phase properties and flow regime.     

Hydrodynamics of non-Newtonian liquids in external-loop airlift bioreactors

Gas holdup investigation was performed in two external-loop airlift bioreactors of laboratory (V _L =1.189·10^?3? 1.880·10^?3 m³; H _R =1.16 ? 1.56 m; H _D = 1.10 m; A _D /A _R = 0.111 ? 1.000) and pilot scale (V _L =0.157?0.170 m³; H _R =4.3?4.7 m; H _D =4.0?4.4 m;A _D /A _R =0.04?0.1225), respectively, using as liquid phase non-Newtonian starch solutions of different concentration with K=0.061?3.518 Pa sⁿ and n=0.86?0.39 and fermentation broths of P. chrysogenum, S. griseus, S. erythreus, B. licheniformis and C. acremonium at different hours since inoculation and from different batches. The influence of bioreactor geometry, liquid properties and the amount of introduced compressed air was investigated. The effect of sparger design on gas holdup was found to be negligible. It was found that gas holdup depends on the flow media index, ?_GR decreasing with the increase of liquid pseudoplasticity, A _D /A _R ratio and H _R /H _D ratio. The experimental data are in agreement with those presented in literature by Popovic and Robinson, which take into account liquid properties, geometric parameters and gas superficial velocity, with a maximum error of ±30%. It was obtained a correlation for gas holdup estimation taking into account the non-Newtonian behaviour of the fermentation broths and the dry weight of the solid phase, as well. The concordance between the experimental data and those calculated with the proposed correlation was good, with a maximum error of ±17%. Also, a dimensionless correlation for gas holdup involving superficial velocities of gas and liquid, cross sectional areas ratio, dispersion height to riser diameter ratio, as well as Froude and Morton numbers, was obtained.     

A modified method for the determination of chemical oxygen demand (COD) for samples with high salinity and low organics

This study proposes a modification to the standard method for the determination of the chemical oxygen demand of samples with a salinity up to 40 g NaCl/L and low organic concentrations (20-230 mg COD/L). The masking of chloride by the use of a HgSO(4):Cl ratio of 20:1 prior to digestion, and the use of 3g K(2)Cr(2)O(7)/L in the digestion solution resulted in an error of less than 10% and 12% for samples containing 40 g NaCl/L at 20-190 mg COD/L and 230 mg COD/L, respectively. Comparison of the standard method with the new proposed method using a synthetic sewage highlights the large errors (50-85%) of the standard method in contrast to an error of less than 10% for the proposed modified method.     

A simple method for the determination of DNA molecular weight distribution

A method is described for the molecular weight distribution of DNA which is determined from sedimentation-velocity analysis. Knowing the distribution of sedimentation coefficients for a single DNA concentration it is possible to extrapolate such a distribution to infinite dilution of the solute in a simple way. Two versions (using two or three terms of a series) of extrapolating equations are considered and discussed in detail. The sedimentation coefficients distribution calculated from these equations differs only insignificantly with that obtained in a conventional way.     

Transport of low molecular weight substances in protein crystals and films

Diffusion of synthetic dyes in lysozyme crystals and bovine serum albumin (BSA) amorphous films is shown to depend on the size of diffusate molecule far more strongly than in solutions. The diffusion coefficient increases from 10(-8) to 10(-13) cm2 sec-1 on about 1.5 divided by 2--fold increase in diffusate dimensions, the diffusion being completely arrested on reaching the limiting dimensions of about 14 A and 12 A for BSA films and lysozyme crystals, respectively. The diffusion in lysozyme crystals is anisotropic, with a diffusion maximum directed along their screw axes. The diffusion coefficient dependence on the charge of diffusate and its binding to proteins is discussed.     

A modified colorimetric method for the determination of pyrrolidone carboxylyl peptidase activity in bacteria

The direct spectrophotometric estimation of ferrocyanide (1) suggested the possibility of measuring small quantities of reducing sugars. However, as previously described (1), the method is not applicable to the measurement of reducing sugars because of the high temperature required for the required oxidation step.Due to the relative differences in molar extinction coefficients at the wavelengths concerned (1,5), the measurement of ferrocyanide rather than ferricyanide (5) provides a large increase in sensitivity.A comparison of such a method with a modified folin-Wu method (2–4) for estimation of blood glucose should indicate the possibility of its application to biological fluids containing cells and proteins.     

Semiquantitative determination of low molecular weight proteinase inhibitors in the presence of high molecular weight inhibitors by a modified radial diffusion assay

The radial diffusion assay is very suitable for the determination of proteinase inhibitors in biological fluids. By combining radial diffusion and ultrafiltration, it has become possible to directly determine low molecular weight proteinase inhibitors in mixtures with inhibitors of higher molecular weight. By this modification the inhibitor solutions to be investigated are not pipetted into wells as usually, but are applied on small pieces of dialysis membranes lying on the gel. The exclusion limit of the membrane must be of a magnitude that the inhibitors of higher molecular weight are retained, whereas the inhibitors of lower molecular weight can diffuse into the gel. The modified method can be used for the direct determination of e.g. aprotinin (Mr 6500) in the presence of alpha 1-proteinase inhibitor (Mr 54,000), ovoinhibitor (Mr 50,000) and ovomucoid (Mr 27,000), respectively. The modified method is suitable for the direct determination of low molecular weight inhibitors of trypsin and papain in serum, synovial fluid and saliva. Tissue extracts containing 4 M guanidine hydrochloride or 6 M urea can be investigated directly, too.